CROSS REFERENCE TO RELATED APPLICATIONS
TECHNICAL FIELD
[0002] The present disclosure is directed to multi-layered films. More specifically, the
present disclosure relates to multi-layered films having gas-barrier properties, methods
of making such multi-layered films, articles incorporating the multi-layered films
(e.g., airbags, fuel hose liners, and vehicle tires), and methods for manufacturing
such articles. The present disclosure also relates to articles of footwear that incorporate
the airbags.
BACKGROUND
[0003] This section provides background information related to the present disclosure which
is not necessarily prior art.
[0004] The design of athletic equipment and apparel as well as footwear involves a variety
of factors from the aesthetic aspects, to the comfort and feel, to the performance
and durability. While design and fashion may be rapidly changing, the demand for increasing
performance in the market is unchanging. To balance these demands, designers employ
a variety of materials and designs for the various components that make up athletic
equipment and apparel as well as footwear.
[0005] Articles of footwear conventionally include an upper and a sole structure. The upper
may be formed from any suitable material(s) to receive, secure, and support a foot
on the sole structure. The upper may cooperate with laces, straps, or other fasteners
to adjust the fit of the upper around the foot. A bottom portion of the upper, proximate
to a bottom surface of the foot, attaches to the sole structure.
[0006] Sole structures generally include a layered arrangement extending between a ground
surface and the upper. One layer of the sole structure includes an outsole that provides
abrasion-resistance and traction with the ground surface. The outsole may be formed
from rubber or other materials that impart durability and wear-resistance, as well
as enhance traction with the ground surface. Another layer of the sole structure includes
a midsole disposed between the outsole and the upper. The midsole provides cushioning
for the foot and may be partially formed from a polymer foam material that compresses
resiliently under an applied load to cushion the foot by attenuating ground-reaction
forces. Sole structures may also include a comfort-enhancing insole or a sockliner
located within a void proximate to the bottom portion of the upper and a strobel attached
to the upper and disposed between the midsole and the insole or sockliner.
US 2020/087512 A1 discloses an article of footwear with a sole stmcture including a bladder.
BRIEF DESCRIPTION OF THE DRAWINGS
[0007] Further aspects of the present disclosure will be readily appreciated upon review
of the detailed description, described below, when taken in conjunction with the accompanying
drawings.
FIG. 1 is a bottom front perspective view of an article of footwear incorporating a multi-layered
film of the present disclosure.
FIG. 2 is an exploded perspective view of the article of footwear shown in FIG. 1.
FIG. 3 is a top schematic view of the article of footwear with an upper of the footwear
omitted for discussion purposes to show a footprint of a midsole chassis and airsole.
FIG. 4A is an expanded side view of a heel region of the airsole in an uncompressed state.
FIG. 4B is an expanded side view of the heel region of the airsole in a compressed state.
FIG. 5 is a sectional view of a multi-layered film of the present disclosure, such as for
use in the article of footwear and the airsole shown in FIGs. 1-4B.
FIG. 6 is an expanded sectional view of a core region of the multi-layered film of the present
disclosure shown in FIG. 5.
FIGs. 7A-7E are sectional views of alternative multi-layered films of the present disclosure.
FIG. 8 shows a spacer component according to one exemplary embodiment of the present disclosure.
FIGs. 9A-9B show an exemplary article of athletic equipment (i.e., a soccer ball; useful for
understanding the invention, but not claimed) incorporating the multi-layered film
of the present disclosure.
FIGs. 10A-10B show a tire (useful for understanding the invention, but not claimed) incorporating
the multi-layered film of the present disclosure.
FIGs. 11A-11C show micrographs illustrating extent of cracking in bladders formed from various
configurations of layers as disclosed herein after being subjected to KIM testing
as described herein.
FIG. 12A shows a comparison of gas transmission rates for a control bladder including 32 EVOH
layers (bottom curve) versus a bladder having 24 EVOH layers with 50 percent thickness
of the control (top curve) and a bladder having 32 EVOH layers with 50 percent thickness
of the control (middle curve). FIGs. 12B-12C are micrographs showing the lack of cracking in the 24 EVOH layer bladder and 32
EVOH layer bladder, respectively, after being subjected to KIM testing as described
herein.
FIG. 13A shows a comparison of gas transmission rates (GTR) for a control bladder including
32 EVOH layers (bottom curve) versus a bladder having 24 EVOH layers with 50 percent
thickness of the control (top curve) and a bladder having 32 EVOH layers with 75 percent
thickness of the control (middle curve). FIG. 13B is a micrograph showing mild cracking in the 32 EVOH layer bladder after being subjected
to KIM testing as described herein.
FIG. 14 shows a comparison of gas transmission rates for a control bladder including 32 EVOH
layers (curve with squares) versus a bladder having 64 EVOH layers with 150 percent
thickness compared to the control (curve with circles) and a bladder having 40 EVOH
layers with approximately the same thickness as the control (curve with triangles).
[0008] Corresponding reference numerals indicate corresponding parts throughout the drawings.
DESCRIPTION
[0009] Claim 1 defines an article of footwear. Claims 2 to 15 define optional features thereof.
The article of footwear comprises a multi-layered film. Thus, the present disclosure
is directed to a multi-layered film (e.g., microlayer film) having thin gas-barrier
layers, which have been found to increase film flexibility while also retaining good
film durability and gas-barrier properties. Such a multi-layered film is particularly
suitable for use in articles that require gas-barrier and/or gas-retention properties
while also being subjected to repeated flexing conditions, such as airbags for use
in footwear cushioning (referred to as "airsoles," as defined below). Thus, the present
claims require that the multi-layered film is in a bladder in a sole structure of
an article of footwear.
[0010] Fluid-filled bladders, including bladders configured for use as cushioning elements,
may be formed from multi-layered films that include gas-barrier layers. The gas-barrier
layers may be brittle enough to develop cracking (and/or crazing) over time. For example,
this may occur after multiple cycles of flexing and release. Cracking (and/or crazing)
may become visible to the naked eye. It may reduce the transparency of one or more
areas of the cushioning element. It may increase the gas transmission rate of the
cushioning element.
[0011] Bladders having bulbous protrusions and/or areas of relatively small radii of curvature
may be more likely to crack. Therefore, these types of bladders are at particular
risk of visible defects. They are also at risk of an unacceptable increase in gas
transmission rate resulting from aligned cracks in many, even all, layers (catastrophic
cracking). There has therefore been a general reluctance in the present field to produce
these types of bladders commercially, particularly bladders which are used as cushioning
elements, as they will be exposed to a very large number of flexing and release cycles
during use.
[0012] Proposals to mitigate increased gas transmission rate due to cracking, and to reduce
the visibility of cracks once they have formed, include increasing the thickness of
individual gas-barrier layers present in the film; and increasing the number of gas-barrier
layers present in the film. Either of these options may lead to an increase in the
overall amount of gas-barrier material present in the multi-layered film.
[0013] In a multi-layered film having a core region including a gas-barrier material, the
core region of the film presents the greatest barrier to rapid diffusion of gas molecules.
When cracks are present in the gas-barrier material forming the gas-barrier layers
of the core region, a gas molecule is able to bypass the gas-barrier material, and
diffuse more rapidly through the more gas-permeable materials present in the film.
When cracks are aligned throughout many or all layers of the core region of a gas-barrier
film, a gas molecule can pass through large portions of the core region of the film
or even through the entire core region of the film in a relatively short amount of
time. Increasing the number of gas-barrier layers decreases the likelihood that cracks
will occur in an aligned manner in a large number of layers or in all layers of the
core. When cracks are not aligned, a gas molecule is forced to take a tortuous path
in order to pass through the overall multi-layered film. A similar effect has been
proposed upon increasing individual gas-barrier layer thicknesses. However, it has
until now not been well understood how to prevent or diminish the formation of cracks
in the gas-barrier layers in the first place.
[0014] Unexpectedly, it has now been found that decreasing the thickness of each individual
gas-barrier layer may prevent or diminish the formation of cracks in the layers. Instead
of using average individual gas-barrier layer thicknesses of several micrometers,
individual average gas-barrier layer thicknesses of less than or equal to 0.75 micrometers,
(particularly of less than or equal to 0.5 micrometers), namely in a range of about
0.01 micrometers to about 0.75 micrometers (particularly, in a range of about 0.01
micrometers to about 0.5 micrometers), are proposed. Average individual gas-barrier
layer thicknesses of below about 0.75 micrometers, and particularly of below about
0.5 micrometers, have been found to reduce cracking and may reduce catastrophic cracking
of the type mentioned above. It has also been found that the use of these thinner
layers in multi-layered films may result in films and bladders that have a gas transmission
rate (that is, without taking into account any cracks, i.e., for films or bladders
prior to exposure to flexing and release) which remains satisfactory compared to the
gas transmission rate of thicker layers. In particular, the gas transmission rate
for the films or bladders may be less than or equal to 4 cubic centimeters per square
meter per day, or less than or equal to 3 cubic centimeters per square meter per day.
[0015] It has surprisingly been found that when these thinner layers are used, it is not
necessary to compensate in other ways. For example, it is not necessary to increase
the overall amount of gas-barrier material, or even to maintain the same overall amount
of gas-barrier material by increasing the number of gas-barrier layers when their
individual thicknesses are reduced. This is in contrast to the proposals to increase
the number of gas-barrier layers or increase the thickness of each individual gas-barrier
layer; both of which tend to lead to an increase in the overall amount of gas-barrier
material.
[0016] It has been found that it is possible to use a relatively low number of gas-barrier
layers, for example about 20 gas-barrier layers (for example, about 24 gas-barrier
layers, thus fewer layers than the 32 gas-barrier layers of the control bladders of
the Examples set out hereinbelow) although more gas-barrier layers may be used, for
example at least 30 gas-barrier layers or at least 40 gas-barrier layers, in order
to provide particularly low gas transmission rates. The number of gas-barrier layers
may optionally be no more than 70. There may be no need for particularly large amounts
of gas-barrier material to be present overall in the multi-layered films.
[0017] The more crack- and craze-resistant multi-layered films disclosed herein may be used
to make bladders (for example, cushioning elements) with a wider variety of shapes
and for a wider variety of uses, than has previously been possible. Cushioning elements
having bulbous protrusions and/or areas of relatively small radii of curvature may
be made, which maintain high clarity and low gas diffusion rates for long periods
of use.
[0018] As used herein, the terms "airbag" and "bladder" are interchangeable and each refers
to either a fluid-inflated and sealed component or a fluid-inflatable and sealable
component, the latter of which can be inflated with one or more fluids and sealed.
As can be appreciated, the sealed and sealable terms can refer to fixed seals (e.g.,
with welded seams) and/or to dynamic seals that can switch between open and closed
states (e.g., with valves). Furthermore, the airbags discussed herein can each have
a single interior cavity that can be inflated with a fluid, multiple interior cavities
that are separate and can be independently inflated with one or more fluids, and/or
multiple interior cavities that are fluidly connected (at least some of them) and
that can be inflated with one or more fluids, and combinations thereof. As further
used herein, the term "airsole" refers to an airbag used as cushioning element in
a footwear midsole component to provide cushioning and/or support to an article of
footwear.
[0019] The shape of a bladder typically includes an upper surface and a lower surface, with
a sidewall positioned between the upper surface and the lower surface. While bladders
may be shaped so that the sidewall includes either convex or concave curved regions,
it is common for the sidewalls to include convex regions which curve away from and
extend beyond the upper surface of the bladder or from the lower surface of the bladder
or from both the upper surface and the lower surface of the bladder. When the bladder
is a midsole component of an article of footwear, the upper surface of the bladder
may be positioned so that it faces the insole of the article of footwear or the cavity
within the upper of the article of footwear configured to contain the foot of a wearer
during use, while the lower surface of the bladder may be positioned so that it faces
the outsole of the article of footwear or the ground. It is common for a curved region
of the sidewall to be visible from the outer surface of the article of footwear, or
even to be exposed and form a portion of the outer surface of the article of footwear.
As used herein, the term "bulbous protrusion" or "bulbous portion" may refer to a
portion or region of a bladder having one or more of the following characteristics,
such as at least two, at least three, or all four of the following characteristics.
The bulbous protrusion or bulbous portion may be a curved sidewall of the bladder,
including a convexly curved sidewall of the bladder. In particular, a bulbous protrusion
or bulbous portion may be a part of a rearwardly and/or laterally extending bladder
in an article of footwear, which projects more than 1 millimeter, optionally more
than 2 millimeters, optionally more than 3mm, optionally more than 4 millimeters,
optionally more than 5 millimeters, beyond the upper or lower surface of the bladder
(alternatively, beyond the rear of the article of footwear) and/or beyond one or more
sides of the article of footwear. When flexed, the bulbous protrusion or portion of
the bladder may extend even further, such as by more than an additional 1 millimeter,
or more than an additional 2 millimeters, or more than an additional 3 millimeters.
Additionally or alternatively, the bulbous protrusion or bulbous portion may be a
concavely or convexly curved surface, particularly a convexly cured surface, having
a curvature that is at least about twice, at least about three times, or even at least
about five times, the minimum curvature found elsewhere in the bladder. Additionally
or alternatively, the bulbous protrusion or bulbous portion may be a concavely or
convexly curved surface (such as a convexly-curved sidewall of a bladder in an article
of footwear), where the height of the curved surface (such as its height when disposed
in an article of footwear) is at least about 50 percent higher, at least about 100
percent higher, or at least about 150 percent higher than the minimum height found
elsewhere in the bladder. Additionally or alternatively, the bulbous protrusion or
bulbous portion may include a concavely or convexly curved surface, particularly a
convexly-curved sidewall, having a radius of curvature that is less than half, less
than a third, or even less than a fifth, of the maximum radius of curvature found
elsewhere in the bladder.
[0020] The multi-layered film or multiple sheets of the multi-layered film can be shaped
into a variety of wall geometries for airbags (e.g., by thermoforming, blow molding,
etc.) and the produced airbag can be inflated with one or more fluids (e.g., one or
more gases) and sealed for use as footwear airsoles.
FEATURES OF THE DISCLOSURE
[0021] Various non-limiting features of the present disclosure will now be described.
[0022] In the multi-layered film disclosed herein, which has one or more core regions, each
of the gas-barrier layers has an average thickness in a range of from about 0.01 to
about 0.75 micrometers, and may particularly have an average thickness in a range
of about 0.01 to about 0.5 micrometers. Each of the elastomeric layers has an average
thickness in a range of from about 2 micrometers to about 8 micrometers, optionally
from about 2 micrometers to about 4 micrometers thick.
[0023] Optionally, the number of gas-barrier layers in each of the one or more core regions
is in a range of from about 20 to about 70; optionally, wherein each of the one or
more core regions comprises at least about 40 layers, optionally from about 50 to
about 100 layers, from about 50 to about 90 layers, from about 50 to about 80 layers,
from about 50 to about 70 layers, from about 60 to about 100 layers, from about 60
to about 90 layers, or from about 60 to about 80 layers.
[0024] Optionally, the gas-barrier material comprises a nitrogen gas-barrier material.
[0025] Optionally, the gas-barrier material comprises or consists essentially of one or
more gas-barrier polymers, and wherein the gas-barrier material comprises a gas-barrier
polymeric component consisting of all polymers present in the gas-barrier material.
[0026] Optionally, the one or more gas-barrier polymers comprise or consist essentially
of one or more thermoplastic vinylidene chloride polymers, one or more thermoplastic
acrylonitrile polymers or copolymers, one or more thermoplastic polyamides, one or
more thermoplastic epoxy resins, one or more thermoplastic amine polymers or copolymers,
or one or more thermoplastic polyolefin homopolymers or copolymers.
[0027] Optionally, the one or more thermoplastic polyolefin homopolymers or copolymers comprise
or consist essentially of one or more thermoplastic polyethylene copolymers.
[0028] Optionally, the one or more thermoplastic polyolefin homopolymers or copolymers comprise
or consist essentially of one or more thermoplastic ethylene-vinyl alcohol copolymers.
[0029] Optionally, the one or more thermoplastic ethylene-vinyl alcohol copolymers include
from about 28 mole percent to about 44 mole percent ethylene content, optionally from
about 32 mole percent to about 44 mole percent ethylene content.
[0030] Optionally, the elastomeric material comprises or consists essentially of one or
more thermoplastic elastomeric polymers, and wherein the elastomeric material comprises
an elastomeric polymeric component consisting of all polymers present in the elastomeric
material.
[0031] Optionally, the one or more thermoplastic elastomeric polymers comprise or consist
essentially of one or more thermoplastic elastomeric polyolefin homopolymers or copolymers,
one or more thermoplastic elastomeric polyamide homopolymers or copolymers, one or
more thermoplastic elastomeric polyester homopolymers or copolymers, one or more thermoplastic
elastomeric polyurethane homopolymers or copolymers, one or more thermoplastic elastomeric
styrenic homopolymers or copolymers, or any combination thereof.
[0032] Optionally, the elastomeric material comprises or consists essentially of one or
more thermoplastic elastomeric polyurethane homopolymers or copolymers, optionally
wherein the elastomeric material comprises or consists essentially of one or more
polydiene polyol-based thermoplastic elastomeric polyurethane homopolymers or copolymers.
[0033] Optionally, the one or more thermoplastic elastomeric polyurethane homopolymers or
copolymers comprise a plurality of first segments derived from one or more polyols
and a plurality of second segments derived from a diisocyanate.
[0034] Optionally, the one or more thermoplastic elastomeric polyurethane homopolymers or
copolymers is a polymerization product of a diisocyanate with one or more polyols.
[0035] Optionally, the thermoplastic elastomeric polyurethane homopolymer or copolymer comprises
or consists essentially of one or more polydiene polyol-based thermoplastic elastomeric
polyurethane homopolymers or copolymers and wherein the polyol comprises or consists
essentially of a polybutadiene polyol, a polyisoprene polyol, a partially or fully
hydrogenated derivative of a polybutadiene polyol or of a polyisoprene polyol, or
any combination thereof.
[0036] Optionally, the one or more polyols comprise or consist essentially of a polyester
polyol, a polyether polyol, a polycarbonate polyol, a polycaprolactone polyether,
or any combination thereof.
[0037] Optionally, the diisocyanate comprises or consists essentially of an aliphatic diisocyanate,
an aromatic diisocyanate, or any combination thereof.
[0038] Optionally, the aliphatic diisocyanate comprises or consists essentially of hexamethylene
diisocyanate (HDI), isophorone diisocyanate (IPDI), butylenediisocyanate (BDI), bisisocyanatocyclohexylmethane
(HMDI), 2,2,4-trimethylhexamethylene diisocyanate (TMDI), bisisocyanatomethylcyclohexane,
bisisocyanatomethyltricyclodecane, norbornane diisocyanate (NDI), cyclohexane diisocyanate
(CHDI), 4,4'-dicyclohexylmethane diisocyanate (H12MDI), diisocyanatododecane, lysine
diisocyanate, or any combination thereof.
[0039] Optionally, the aromatic diisocyanate comprises or consists essentially of toluene
diisocyanate (TDI), TDI adducts with trimethylolpropane (TMP), methylene diphenyl
diisocyanate (MDI), xylene diisocyanate (XDI), tetramethylxylylene diisocyanate (TMXDI),
hydrogenated xylene diisocyanate (HXDI), naphthalene 1,5-diisocyanate (NDI), 1,5-tetrahydronaphthalene
diisocyanate, para-phenylene diisocyanate (PPDI), 3,3'-dimethyldiphenyl-4,4'-diisocyanate
(DDDI), 4,4'-dibenzyl diisocyanate (DBDI), 4-chloro-1,3-phenylene diisocyanate, or
any combination thereof.
[0040] Optionally, the gas-barrier material has a melt flow index of from about 5 to about
7 grams per 10 minutes at 190 degrees Celsius when using a weight of 2.16 kilograms.
[0041] Optionally, the elastomeric material has a melt flow index of from about 20 to about
30 grams per 10 minutes at 190 degrees Celsius when using a weight of 2.16 kilograms.
[0042] Optionally, the melt flow index of the gas-barrier material is from about 80 percent
to about 120 percent of the melt flow index of the elastomeric material, optionally
from about 90 percent to about 110 percent of the melt flow index of the elastomeric
material, from about 95 percent to about 105 percent of the melt flow index of the
elastomeric material, or wherein the melt flow index of the gas-barrier material is
substantially the same as the melt flow index of the elastomeric material, wherein
the melt flow index is measured in cubic centimeters per 10 minutes at 190 degrees
Celsius when using a weight of 2.16 kilograms.
[0043] Optionally, the gas-barrier material has a melting temperature of from about 165
degrees Celsius to about 183 degrees Celsius.
[0044] Optionally, the elastomeric material has a melting temperature of from about 155
degrees Celsius to about 165 degrees Celsius.
[0045] Optionally, the melting temperature of the gas-barrier material is within about 10
degrees Celsius of the melting temperature of the elastomeric material, optionally
within about 8 degrees Celsius of the melting temperature of the elastomeric material,
or within about 5 degrees Celsius of the melting temperature of the elastomeric material.
[0046] Optionally, the blended material comprises or consists essentially of a blend of
one or more additional thermoplastic elastomers and a second material, optionally
wherein the second material comprises or consists essentially of one or more second
polymers, optionally wherein the one or more second polymers comprise or consist essentially
of one or more second thermoplastics.
[0047] Optionally, the one or more second thermoplastics comprise one or more thermoplastic
polyolefin homopolymers or copolymers, one or more thermoplastic polyamide homopolymers
or copolymers, one or more thermoplastic polyester homopolymers or copolymers, one
or more thermoplastic polyurethane homopolymers or copolymers, one or more thermoplastic
styrenic homopolymers or copolymers, or any combination thereof.
[0048] Optionally, the one or more second thermoplastics comprise or consist essentially
of thermoplastic polypropylene homopolymers or copolymers, thermoplastic polyethylene
homopolymers or copolymers, thermoplastic polybutylene homopolymers or copolymers,
or any combination thereof.
[0049] Optionally, the one or more second thermoplastics comprise or consist essentially
of one or more thermoplastic polyethylene copolymers.
[0050] Optionally, the one or more second thermoplastics comprise or consist essentially
of one or more thermoplastic ethylene-vinyl alcohol copolymers.
[0051] Optionally, a polymeric component of the blended material consists of one or more
additional thermoplastic elastomeric polyurethane homopolymers or copolymers, and
one or more second thermoplastic ethylene-vinyl alcohol copolymers.
[0052] Optionally, the polymeric component of the thermoplastic elastomeric material consists
of one or more additional thermoplastic elastomeric polyester-polyurethane copolymers
and one or more second thermoplastic ethylene-vinyl alcohol copolymers.
[0053] Optionally, the blended material comprises one or more recycled additional thermoplastic
elastomers, or one or more recycled second thermoplastics, or both.
[0054] Optionally, the blended material is a phase-separated blend of the one or more additional
thermoplastic elastomers and the one or more second thermoplastics.
[0055] Optionally, the phase-separated blend includes one or more phase-separated regions
including interfaces between the one or more additional thermoplastic elastomers and
the one or more second thermoplastics.
[0056] Optionally, the blend comprises about 95 percent by weight of the one or more additional
thermoplastic elastomers and about 5 percent by weight of the one or more second thermoplastics
based on a total weight of the blend.
[0057] Optionally, the one or more recycled polymers comprise one or more recycled thermoplastics,
optionally wherein the one or more recycled thermoplastics comprise one or more recycled
thermoplastic elastomers; optionally wherein the recycled material comprises a recycled
material polymeric component consisting of one or more recycled thermoplastics, optionally
wherein the recycled material polymeric component comprises or consists essentially
of one or more recycled thermoplastic elastomers.
[0058] Optionally, the recycled material comprises one or more recycled thermoplastic elastomers,
optionally wherein the one or more recycled thermoplastic elastomers comprise one
or more reground thermoplastic elastomers, optionally wherein the one or more recycled
or reground thermoplastic elastomers includes a thermoplastic elastomeric material
according to any one of paragraphs [0045] to [0054].
[0059] Optionally, the recycled material further comprises one or more recycled second thermoplastics,
optionally wherein the one or more recycled second thermoplastics comprise one or
more reground second thermoplastics, optionally wherein the one or more recycled or
reground second thermoplastics include a thermoplastic according to any one of paragraphs
[0061] to [0064].
[0060] Optionally, the recycled material comprises one or more recycled or reground thermoplastic
polyurethane elastomers or one or more recycled or reground thermoplastic ethylene-vinyl
alcohol copolymers or both.
[0061] Optionally, the recycled material comprises a blend of the one or more recycled or
reground thermoplastic elastomers and one or more second thermoplastics, or wherein
the recycled material comprises a blend of one or more thermoplastic elastomers and
one or more recycled thermoplastics or one or more recycled second thermoplastics,
optionally wherein the blend is a phase-separated blend, and optionally wherein the
phase-separated blend comprises one or more interfaces between the one or more recycled
thermoplastic elastomers and the one or more second thermoplastics.
[0062] Optionally, the recycled material comprises about 99 percent to about 90 percent
by weight of the one or more recycled thermoplastic elastomers and about 1 percent
to about 10 percent by weight of the one or more second thermoplastics based on a
total weight of the recycled material, optionally wherein the recycled material comprises
about 99 percent to about 93 percent by weight of the one or more recycled thermoplastic
elastomers and about 1 percent to about 7 percent by weight of the one or more second
thermoplastics, or about 99 percent to about 95 percent by weight of the one or more
recycled thermoplastic elastomers and about 1 percent to about 5 percent by weight
of the one or more second thermoplastic elastomers.
[0063] Optionally, the recycled material comprises about 99 percent to about 50 percent
by weight of recycled or reground polymers based on a total weight of recycled material,
optionally from about 99 percent to about 75 percent by weight of recycled or reground
polymers.
[0064] Optionally, the recycled material further comprises one or more virgin first thermoplastic
elastomers, optionally wherein the one or more virgin first thermoplastic elastomers
includes one or more virgin thermoplastic polyurethane elastomers.
[0065] Optionally, the multi-layered film further comprises one or more tie layers, each
of the one or more tie layers individually comprising or consisting essentially of
a tie material, wherein the one or more tie layers increase a bond strength between
two adjacent layers.
[0066] Optionally, the tie material of each of the one or more tie layers independently
comprises or consists essentially of a polyurethane, a polyacrylate, an ethylene-acrylate
copolymer, a maleic anhydride grafted polyolefin, or any combination thereof, optionally
wherein the tie material comprises or consists essentially of a blended material according
to any of paragraphs [0061] to [0071] or a recycled material according to any of paragraphs
[0072] to [0079].
[0067] Optionally, the tie material of the one or more tie layers independently comprises
or consists essentially of one or more thermoplastic polyurethane elastomeric homopolymers
or copolymers, optionally wherein the one or more tie layers comprise or consist essentially
of a polydiene polyol-based thermoplastic polyurethane.
[0068] Optionally, the multi-layered film further comprises one or more structural layers,
each of the one or more structural layers independently comprising or consisting essentially
of a structural layer material, optionally wherein the structural layer material comprises
or consists essentially of a blended material as described herein.
[0069] Optionally, the structural layer material of each of the one or more structural layers
independently comprises or consists essentially of a polydiene polyol-based thermoplastic
polyurethane.
[0070] Optionally, the elastomeric material of the one or more core regions is a first elastomeric
material, wherein the multi-layered film further comprises a second elastomeric material,
and wherein the formed multi-layered film further comprises:
a first structural layer secured to a first side of one of the one or more core regions,
optionally wherein the first structural layer comprises the second elastomeric material
and optionally has an average thickness ranging from about 900 micrometers to about
1990 micrometers; and
a second structural layer secured to a second side of the core region that is opposing
to the first side of the core region, optionally wherein the second structural layer
comprises the second elastomeric material and optionally has an average thickness
ranging from about 900 micrometers to about 1990 micrometers.
[0071] Optionally, the multi-layered film further comprises one or more cap layers, wherein
the one or more cap layers comprise or consist essentially of a cap layer material,
optionally wherein the cap layer material comprises or consists essentially of a blended
material according to any of paragraphs [0061] to [0071] or a recycled material according
to any of paragraphs [0072] to [0079].
[0072] Optionally, the cap layer material of the one or more cap layers comprises or consists
essentially of a polyurethane, a polyacrylate, an ethylene-acrylate copolymer, a maleic
anhydride grafted polyolefin, or any combination thereof.
[0073] Optionally, the cap layer material of the one or more cap layers comprises or consists
essentially of a thermoplastic polyurethane, optionally a polydiene polyol-based thermoplastic
polyurethane.
[0074] Optionally, at least one of the one or more tie layers is positioned between one
of the one or more structural layers and one of the one or more core regions.
[0075] Optionally, at least one of the one or more structural layers is positioned between
one of the one or more tie layers and one of the one or more cap layers.
[0076] Optionally, the multi-layered film is a coextruded layered sheet, or a laminated
layered sheet.
[0077] Optionally, the multi-layered film comprises a first cap layer, a first structural
layer, a first tie layer, a core region, a second tie layer, a second structural layer,
and a second cap layer, wherein a first cap layer inner surface contacts a first surface
of the first structural layer, a second surface of the first structural layer contacts
a first surface of the first tie layer, a second surface of the first tie layer contacts
a first surface of the core region, a second surface of the core region contacts a
first surface of the second tie layer, a second surface of the second tie layer contacts
a first surface of the second structural layer, and a second surface of the second
structural layer contacts an inner layer of the second cap layer.
[0078] Optionally, the multi-layered film has a structure of A-B-C-B-A, wherein A represents
a structural layer, B represents a tie layer, and C represents a core region.
[0079] Optionally, the multi-layered film has a structure of D-A-B-C-B-A-D, wherein A represents
a structural layer, B represents a tie layer, C represents a core region, and D represents
a cap layer.
[0080] Optionally, the one or more core regions has a gas transmission rate of from about
0.3 to about 1.9 cubic centimeters per square meter per day for nitrogen measured
at 23 degrees Celsius and 0 percent relative humidity for a structure having a thickness
of from about 72 micrometers to about 320 micrometers, optionally wherein each of
the one or more core regions has a gas transmission rate of from about 0.3 to about
1.9 cubic centimeters per square meter per day for nitrogen measured at 23 degrees
Celsius and 0 percent relative humidity.
[0081] Optionally, the multi-layered film comprises one or more protective layers, each
of the one or more protective layers individually comprising or consisting essentially
of a protective material, wherein each of the one or more protective layers is adjacent
to a core region and has a protective layer thickness, wherein a combination of the
one or more protective layers and the adjacent core region has a minimum radius of
curvature which is greater than a minimum radius of curvature which causes cracking
of the core region, or of one or more individual layers within the core region.
[0082] The multi-layered film may be made by a method comprising:
co-extruding the gas-barrier material and the elastomeric material to form the multi-layered
film.
[0083] Optionally, the method further comprises:
co-extruding at least one tie layer with the multi-layered film comprising the core
region to form a multi-layered film comprising the one or more core regions and the
tie layer.
[0084] Optionally, the method further comprises:
applying at least one structural layer to the multi-layered film comprising the core
region and the tie layer to form a multi-layered film comprising the one or more core
regions, the tie layer, and the structural layer, wherein the structural layer comprises
a structural layer material as described herein.
[0085] Optionally, the method further comprises:
co-extruding at least one structural layer with the multi-layered film comprising
the core region and the tie layer to form a multi-layered film comprising the one
or more core regions, the tie layer, and the structural layer.
[0086] Optionally, the method further comprises:
co-extruding at least one cap layer with the multi-layered film comprising the core
region, the tie layer, and the structural layer to form a multi-layered film comprising
the core region, the tie layer, the structural layer, and the cap layer.
[0087] Also disclosed herein is an article of footwear comprising the multi-layered film,
wherein the article comprises a series of three or more layers, including:
a first cap layer comprising or consisting essentially of a first cap layer material,
the first cap layer including a first cap layer outer surface defining a first outer
surface of the multi-layered film, a first cap layer inner surface opposing the first
cap layer outer surface, a first cap layer thickness extending from the first cap
layer inner surface to the first cap layer outer surface, wherein the first cap layer
outer surface defines a first exterior surface of the article;
optionally, a second cap layer comprising or consisting essentially of a second cap
layer material, the second cap layer including a second cap layer outer surface defining
a second outer surface of the multi-layered film, a second cap layer inner surface
opposing the second cap layer outer surface, a second cap layer thickness extending
from the second cap layer inner surface to the second cap layer outer surface, optionally
wherein the second cap layer outer surface defines a second exterior surface of the
article; and
the one or more core regions, each of the one or more core regions including a core
region first surface, a core region second surface, and a core region thickness extending
from the core region first surface to the core region second surface, wherein each
of the one or more core regions is positioned between the first cap layer inner surface
and the second cap layer inner surface.
[0088] Optionally, in the multi-layered film, the second cap layer is present and wherein
the first cap layer material and the second cap layer material are substantially the
same.
[0089] Optionally, in the multi-layered film, the second cap layer is present and wherein
the first cap layer material and the second cap layer material are different.
[0090] Optionally, in the multi-layered film, the first cap layer inner surface is in contact
with the core region first surface, or the optional second cap layer inner surface
is in contact with the core region second surface, or both.
[0091] Optionally the multi-layered film of the article is configured as a series of four
of more layers including one or more structural layers, each of the one or more structural
layers comprising a structural layer material and including a structural layer first
surface, a structural layer second surface opposing the structural layer first surface,
and a structural layer thickness extending from the structural layer first surface
to the structural layer second surface;
optionally wherein at least one of the one or more structural layers is positioned
between the first cap layer and the core region, or between the second cap layer and
the core region; or
optionally wherein the one or more structural layers comprise two or more structural
layers, and at least a first one of the two or more structural layers is positioned
between an inner surface of a first cap layer and the first surface of a core region,
and at least a second one of the two or more structural layers is positioned between
a second surface of a core region and the inner surface of the second cap layer.
[0092] Optionally, in the multi-layered film, a first surface of a first one of the structural
layers is in contact with the inner surface of the first cap layer, and the second
surface of the first one of the structural layers is in contact with a first surface
of one of the one or more core regions, or wherein the first surface of a second one
of the one or more structural layers is in contact with the second surface of one
of the one or more core regions, and the second surface of the second one of the structural
layers is in contact with an inner surface of the second cap layer, or both.
[0093] Optionally, in the multi-layered film, the one or more structural layers comprise
or consist essentially of the blended material of any one of paragraphs [0061] to
[0071].
[0094] Optionally, in the multi-layered film, the one or more structural layers comprise
or consist essentially of the recycled material of any one of paragraphs [0072] to
[0079].
[0095] Optionally the multi-layered film of the article is configured as a series of five
or more layers including one or more tie layers, each of the one or more tie layers
including a tie layer first surface, a tie layer second surface opposing the tie layer
first surface, and a tie layer thickness extending from the tie layer first surface
to the tie layer second surface;
optionally wherein at least one of the one or more tie layers is positioned between
one of the one or more structural layers and one of the one or more core regions,
or between the first cap layer and one of the one or more structural layers, or between
the second cap layer and one of the one or more structural layers, or any combination
thereof; or
optionally wherein the one or more tie layers comprise two or more tie layers, and
at least a first one of the two or more tie layers is positioned between a second
surface of a first structural layer and a first layer of a core region, and at least
a second one of the two or more tie layers is positioned between a second surface
of a core region and a first surface of a structural layer.
[0096] Optionally, in the multi-layered film, a first surface of a first one of the one
or more tie layers is in contact with a second surface of a first one of the one or
more structural layers, and the second surface of the first one of the one or more
tie layers is in contact with a first surface of a core region; or wherein a first
surface of a second one of the one or more tie layers is in contact with a second
surface of one of the one or more core regions, and the second surface of the second
one of the one or more tie layers is in contact with a first surface of a second one
of the one or more structural layers, or both.
[0097] Optionally the multi-layered film of the article comprises a first cap layer, a first
structural layer, a first tie layer, a core region, a second tie layer, a second structural
layer, and a second cap layer, wherein the first cap layer inner surface contacts
the first surface of the first structural layer, the second surface of the first structural
layer contacts the first surface of the first tie layer, the second surface of the
first tie layer contacts the first surface of the core region, the second surface
of the core region contacts the first surface of the second tie layer, the second
surface of the second tie layer contacts the first surface of the second structural
layer, and the second surface of the second structural layer contacts the inner layer
of the second cap layer.
[0098] Optionally the multi-layered film forms an external-facing layer of a cushioning
element in the article of footwear.
[0099] Optionally the multi-layered film is effective at retaining a fluid in the cushioning
element.
[0100] The multi-layered film may be made by a method comprising:
co-extruding gas-barrier material and elastomeric material to form a multi-layered
film comprising the one or more core regions.
[0101] Optionally, the method further comprises:
applying at least one tie layer to the multi-layered film comprising the one or more
core regions to form a multi-layered film comprising the one or more core regions
and the tie layer, wherein the tie layer comprises a tie material as described herein.
[0102] Optionally, the method further comprises:
co-extruding at least one tie layer with the multi-layered film comprising the core
region to form a multi-layered film comprising the one or more core regions and the
tie layer.
[0103] Optionally, the method further comprises:
applying at least one structural layer to the multi-layered film comprising the core
region and the tie layer to form a multi-layered film comprising the one or more core
regions, the tie layer, and the structural layer, wherein the structural layer comprises
a structural layer material as described herein.
[0104] Optionally, the method further comprises:
co-extruding at least one structural layer with the multi-layered film comprising
the core region and the tie layer to form a multi-layered film comprising the one
or more core regions, the tie layer, and the structural layer.
[0105] Optionally, the method further comprises:
applying at least one cap layer to the multi-layered film comprising the core region,
the tie layer, and the structural layer to form a multi-layered film comprising the
core region, the tie layer, the structural layer, and the cap layer, wherein the cap
layer comprises a cap layer material as described herein.
[0106] Optionally, the method further comprises:
co-extruding at least one cap layer with the multi-layered film comprising the core
region, the tie layer, and the structural layer to form a multi-layered film comprising
the core region, the tie layer, the structural layer, and the cap layer.
[0107] The bladder for an article of footwear disclosed herein may comprise:
a first sheet; and
a second sheet,
wherein the first sheet, or the second sheet, or each of the first sheet and the second
sheet comprise the multi-layered film disclosed herein,
wherein a first side of the first sheet faces a second side of the second sheet,
wherein the first sheet and the second sheet are joined together by a bond to form
an internal cavity in a space between the first side of the first sheet and the second
side of the second sheet,
wherein the bond extends around at least a portion of a perimeter of the internal
cavity, optionally wherein the bond is contiguous around only one or more portions
of the perimeter of the internal cavity, and includes one or more apertures capable
of admitting a gas to the internal cavity, forming an open cavity; or wherein the
bond is contiguous around an entire perimeter of the internal cavity, forming a sealed
bladder capable of retaining a gas in the internal cavity at a pressure above atmospheric
pressure, at atmospheric pressure, or below atmospheric pressure; particularly, above
or at atmospheric pressure.
[0108] Optionally, the first sheet and the second sheet are adhesively bonded or are thermally
bonded, optionally wherein bladder includes a thermal bond formed by radio frequency
welding between the first sheet and the second sheet.
[0109] Optionally, the bond is contiguous around the entire perimeter of the internal cavity
and the internal cavity comprises a gas, optionally wherein the gas is a pressurized
gas.
[0110] Optionally, the gas comprises nitrogen gas or air.
[0111] Optionally, the internal cavity has an initial internal pressure of from about 20
pounds per square inch (137.9 kilopascals) to about 22 pounds per square inch (151.7
kilopascals).
[0112] Optionally, after 2 years of use, the internal cavity has an inflation pressure of
from at least about 70 percent to about 80 percent of the initial internal pressure.
[0113] Each of the gas-barrier layers has an average thickness ranging from about 0.01 micrometer
to about 0.75 micrometers, particularly in a range of from about 0.01 micrometers
to about 0.5 micrometers.
[0114] Each of the elastomeric layers has an average thickness ranging from about 2 micrometers
to about 8 micrometers.
[0115] Optionally, the core region comprises at least 30, or at least 40, or at least 50
gas-barrier layers; optionally up to 70 gas-barrier layers.
[0116] Optionally, the plurality of elastomeric layers comprises at least 50 elastomeric
layers.
[0117] Optionally, the average total thickness of the core region ranges from about 125
micrometers to about 200 micrometers, and the multi-layered film further comprises:
a first structural layer secured to a first side of the core region, optionally wherein
the first structural layer has an average thickness ranging from about 900 micrometers
to about 1990 micrometers; and
a second structural layer secured to a second side of the core region that is opposing
to the first side of the core region, optionally wherein the second structural layer
has an average thickness ranging from about 900 micrometers to about 1990 micrometers.
[0118] Optiohnally, the structural layer material of each of the one or more structural
layers independently comprises or consists essentially of a polydiene polyol-based
thermoplastic polyurethane.
[0119] Optionally, the bladder further comprises one or more cap layers, wherein the one
or more cap layers comprise or consist essentially of a cap layer material.
[0120] Optionally, the cap layer material of the one or more cap layers comprises or consists
essentially of a polyurethane, a polyacrylate, an ethylene-acrylate copolymer, a maleic
anhydride grafted polyolefin, or any combination thereof.
[0121] Optionally, each cap layer has a thickness ranging from about 5 micrometers to about
25 micrometers.
[0122] The bladder may further comprise one or more tie layers, each of the one or more
tie layers individually comprising or consisting essentially of a tie material, wherein
the one or more tie layers increase a bond strength between two adjacent layers.
[0123] The tie material of each of the one or more tie layers may independently comprise
or consist essentially of a polyurethane, a polyacrylate, an ethylene-acrylate copolymer,
a maleic anhydride grafted polyolefin, or any combination thereof.
[0124] Optionally, each of the one or more tie layers has an average thickness ranging from
about 5 micrometers to about 20 micrometers.
[0125] Optionally, the bladder is configured as an airsole for an article of footwear and
wherein the bladder comprises one or more bulbous protrusions.
[0126] Optionally, the one or more bulbous protrusions are found in a heel portion of the
airsole, a lateral portion of the airsole, a medial portion of the airsole, or any
combination thereof.
[0127] Optionally, the bladder comprises:
a first sheet; and
a second sheet,
wherein the first sheet, or the second sheet, or each of the first sheet and the second
sheet, comprise the multi-layered film,
wherein a first side of the first sheet faces a second side of the second sheet,
wherein the first sheet and the second sheet are joined together by a bond at discrete
locations.
[0128] Optionally, the bond between the first sheet and the second sheet forms
a substantially U-shaped first chamber; and
a substantially U-shaped second chamber, the second chamber being spaced apart from
the first chamber in a direction extending along a longitudinal axis of the bladder.
[0129] Optionally, the first chamber and the second chamber are in gas communication with
one another.
[0130] Optionally, the first chamber is aligned with the second chamber in the direction
extending along the longitudinal axis of the bladder.
[0131] Optionally, the first chamber includes a first leg and a second leg joined by a first
arcuate segment and the second chamber includes a third leg and a fourth leg joined
by a second arcuate segment.
[0132] Optionally, the first leg, the second leg, the third leg, and the fourth leg extend
in the same direction.
[0133] Optionally, the first leg and the second leg are disposed between the first arcuate
segment and the second arcuate segment.
[0134] Optionally, at least one of the first leg, the second leg, the third leg, or the
fourth leg is elongate.
[0135] The bladder may further comprise a third chamber extending between the first leg
and the second leg in a direction toward the first arcuate segment.
[0136] Optionally, the third chamber is spaced apart from the first leg and the second leg.
[0137] The bladder may further comprise a fourth chamber extending between the third leg
and the fourth leg in a direction toward the second arcuate segment.
[0138] Optionally, the fourth chamber is spaced apart from the third leg and the fourth
leg.
[0139] Optionally, at least one of the third chamber or the fourth chamber is elongate.
[0140] The bladder may further comprise a web area defining the first chamber and the second
chamber.
[0141] Optionally, the web area includes a first portion that is substantially U-shaped
and a second portion that is substantially U-shaped.
[0142] Optionally, the bladder does not exhibit cracking after at least 350,000 KIM cycles,
or at least 400,000 KIM cycles.
[0143] Optionally, the bladder has a gas transmission rate of no more than 120 percent of
an original gas transmission rate after 320,000 KIM cycles.
[0144] Optionally, the bladder has a gas transmission rate of from about 0.5 to about 2
cubic centimeters per square meter per day for nitrogen measured at 23 degrees Celsius
and 0 percent relative humidity for a structure having a thickness of from about 72
micrometers to about 320 micrometers after from about 0 KIM cycles to about 320,000
KIM cycles.
[0145] Optionally, the bladder is a thermoformed bladder.
[0146] Optionally, the multi-layered film or the bladder further comprises a decorative
element.
[0147] A decorative element may be applied to the multi-layered film by a method comprising
applying the decorative element by printing, painting, brushing, or spraying the decorative
element onto the multi-layered film or bladder; or dipping the multi-layered film
or bladder into the decorative element; or pressing the decorative element and the
multi-layered film or bladder together, wherein the decorative element is in the form
of a solid, a liquid, or a gas when applied to the multi-layered film or bladder,
optionally wherein the decorative element comprises a pigment or a dye or both a pigment
and a dye.
[0148] Optionally, the decorative element comprises pigments or dyes or both, and the step
of applying the decorative element onto the multi-layered film or bladder comprises
curing the decorative element on the multi-layered film or bladder, optionally wherein
the curing comprises drying the decorative element, or crosslinking the decorative
element, or infusing at least a portion of the decorative element into a polymeric
material of an exterior surface of the multi-layered film or bladder, or bonding the
decorative element to the exterior surface of the multi-layered film or bladder, or
any combination thereof.
[0149] Optionally, the method comprises the step of bonding the decorative element to the
exterior surface of the multi-layered film or bladder, and the bonding includes forming
an adhesive bond by applying an adhesive to a first side of the decorative element
or to the exterior surface of the multi-layered film or bladder, or both, and then
pressing together the first side of the decorative element and the exterior surface
of the multi-layered film or bladder.
[0150] Optionally, the method comprises the step of bonding the decorative element to the
exterior surface of the multi-layered film or bladder, and the bonding includes forming
a thermal bond between a thermoplastic material of a first side of the decorative
element and a thermoplastic material defining the exterior surface of the multi-layered
film or bladder, by softening or melting at least an outer portion of one or both
of the thermoplastic materials, and pressing the first side of the decorative element
and the exterior surface of the multi-layered film or bladder against each other while
the one or both of the thermoplastic materials are softened or melted, and then re-solidifying
the softened or melted outer portion.
[0151] Optionally, the decorative element is applied to an exterior surface of the multi-layered
film or bladder, and, during applying or during the curing or during both the applying
and the curing, the decorative element infuses into a material defining the exterior
surface of the multi-layered film or bladder, optionally wherein the decorative element
is applied as a solution of a dye.
[0152] Optionally, the internal cavity of the bladder further comprises a spacer component.
[0153] Optionally, the spacer component comprises a foamed component, an injection molded
component, a 3D printed component, a textile component, or any combination thereof.
[0154] Optionally, the foamed component comprises a plurality of foam particles.
[0155] Optionally, the spacer component comprises:
a first layer;
a second layer; and
a plurality of connecting members extending between and joining the first layer and
the second layer.
[0156] Optionally, the internal cavity of the bladder is hollow.
[0157] Optionally, the bladder further comprises a textile.
[0158] Optionally, the textile forms a layer of the first sheet, a layer of the second sheet,
or layers of both the first sheet and the second sheet.
[0159] Optionally, the textile forms an outer layer of the first sheet and/or an outer layer
of the second sheet, or wherein the textile forms an inner layer of the first sheet
and/or an inner layer of the second sheet.
[0160] Optionally, the textile is a spacer textile having a first textile face, a second
textile face, and a textile thickness extending from the first textile face to the
second textile face, wherein the textile thickness is from about 0.3 centimeters to
about 3 centimeters, or from about 0.5 centimeters to about 1 centimeter, optionally
wherein a fiber density of the first textile face and the second textile face is at
least 25 percent greater, or at least 50 percent greater, or at least 75 percent greater
than a fiber density between the first textile face and the second textile face.
[0161] Optionally, fibers or yarns of the textile comprise or consist essentially of synthetic
fibers or yarns formed from one or more thermoplastic materials, optionally wherein
the thermoplastic materials of the synthetic fibers or yarns comprise or consist essentially
of a thermoplastic elastomeric material.
[0162] Optionally, a melting temperature of the thermoplastic material of the synthetic
fibers or yarns is within 20 degrees Celsius of a melting temperature of a thermoplastic
material forming an outer layer of the bladder.
[0163] Optionally, the first sheet, the second sheet, or both comprise a layered sheet,
and a polymeric component of the thermoplastic material of the synthetic fibers or
yarns is substantially the same as a polymeric component of a thermoplastic material
of one or more layers of the first sheet and/or one or more layers of the second sheet,
optionally wherein the polymeric component of the thermoplastic material of the synthetic
fibers or yarns is substantially the same as a polymeric component of a thermoplastic
material of a cap layer or of a structural layer of the first sheet and/or a cap layer
or a structural layer of the second sheet.
[0164] Optionally, the cushioning element is a cushioning element for a consumer good, optionally
wherein the cushioning element is a cushioning element for an article of apparel,
an article of footwear, or an article of sporting equipment.
[0165] Optionally, the cushioning element is a cushioning element for an article of footwear,
and the cushioning element for an article of footwear is an airsole.
[0166] The disclosed sole structure for an article of footwear having an upper may comprise:
a heel region disposed in a posterior end;
a forefoot region disposed in an anterior end;
a mid-foot region disposed intermediately between the heel region and the forefoot
region; and
the bladder.
[0167] The bladder may be disposed in the heel region.
[0168] Optionally, the article of footwear further comprises a chassis secured to the upper.
[0169] Optionally, the article of footwear further comprises an outsole, optionally wherein
the outsole is secured to the bladder.
[0170] Optionally, the bladder is disposed between the chassis and the outsole.
[0171] The article of footwear may have a forefoot region, a midfoot region, and a heel
region along a longitudinal axis of the article of footwear, the article of footwear
comprising:
an upper; and
a sole structure including the bladder; optionally, wherein the bulbous portion has
a first height in an uncompressed state and a second height in a compressed state,
the second height being less than 50 percent of the first height.
[0172] Optionally, the bulbous portion of the bladder is a bulbous heel portion, and is
in a heel region of the article of footwear.
[0173] Optionally, the bladder comprises a second multi-layered film, optionally wherein
a structure of the second multi-layered film differs from a structure of the first
multi-layered film in number of gas-barrier layers and elastomeric layers, or differs
in thickness of gas-barrier layers and elastomeric layers, or differs in both number
and thickness of gas-barrier layers and elastomeric layers.
[0174] Optionally, the plurality of gas-barrier layers comprises at least 30 or at least
40 gas-barrier layers; and, optionally, up to 70 gas-barrier layers.
[0175] Optionally, the plurality of gas-barrier layers comprises at least 50 gas-barrier
layers.
[0176] Optionally, an average total thickness of the plurality of gas-barrier layers and
the plurality of elastomeric layers is less than 200 micrometers.
[0177] Optionally, the average total thickness of the plurality of gas-barrier layers and
the plurality of elastomeric layers is less than 175 micrometers.
[0178] Optionally, the first height ranges from about 10 millimeters to about 24 millimeters.
[0179] Optionally, the first height ranges from about 15 millimeters to about 24 millimeters.
[0180] Optionally, the second height ranges from about 8.6 millimeters to about 13.6 millimeters.
[0181] Optionally, the second height ranges from about 8.6 millimeters to about 11 millimeters.
[0182] Optionally, the plurality of gas-barrier layers compositionally comprise one or more
thermoplastic vinylidene chloride polymers, one or more thermoplastic acrylonitrile
polymers or copolymers, one or more thermoplastic polyamides, one or more thermoplastic
epoxy resins, one or more thermoplastic amine polymers or copolymers, one or more
thermoplastic polyolefin homopolymers or copolymers, or any combination thereof.
[0183] Optionally, the plurality of gas-barrier layers compositionally comprise ethylene
vinyl alcohol.
[0184] Optionally, the plurality of elastomeric layers compositionally comprise one or more
thermoplastic elastomeric polymers.
[0185] Optionally, the plurality of elastomeric layers compositionally comprise a polyolefin
copolymer, a polyester, a thermoplastic polyurethane, a styrenic block copolymer,
or any combination thereof.
[0186] Optionally, the plurality of elastomeric layers compositionally comprise a thermoplastic
polyurethane.
[0187] Optionally, the multi-layered film further comprises at least one structural layer
having an average thickness ranging from about 900 micrometers to about 1990 micrometers.
[0188] Optionally, the bulbous heel portion extends a first rearward distance beyond the
outsole in the uncompressed state and a second rearward distance beyond the outsole
in the compressed state, and wherein a difference between the first rearward distance
and the second rearward distance ranges from about 1.1 millimeters to about 1.9 millimeters.
[0189] Optionally, the difference between the first rearward distance and the second rearward
distance ranges from about 1.1 millimeters to about 1.5 millimeters.
[0190] Optionally, a geometry of the bulbous heel portion in the uncompressed state defines
a first vector extending from a rearward-most point of the uncompressed bulbous heel
portion to a rearward-most point of the midsole chassis, and a second vector extending
from the rearward-most point of the uncompressed bulbous heel portion to a rearward-most
point of the outsole, and wherein the first vector and the second vector extends from
each other at an angle ranging from about 115 degrees to about 137.5 degrees.
[0191] Optionally, a geometry of the bulbous heel portion in the compressed state defines
a third vector extending from a rearward-most point of the compressed bulbous heel
portion to the rearward-most point of the midsole chassis, and a fourth vector extending
from the rearward-most point of the compressed bulbous heel portion to the rearward-most
point of the outsole, and wherein the third vector and the fourth vector extends from
each other at an angle ranging from about 38 degrees to about 107 degrees.
[0192] Optionally, a gas is retained within the airsole.
[0193] Optionally, the airsole has an initial inflation pressure ranging from about 20 pounds
per square inch (137.9 kilopascals) to about 22 pounds per square inch (151.7 kilopascals).
[0194] Optionally, the multi-layered film is configured such that, after 1 year of use,
the airsole retains an inflation pressure of at least about 70 percent of the initial
inflation pressure, of at least 80 percent of the initial inflation pressure, or of
at least 90 percent of the initial inflation pressure.
[0195] Optionally, the multi-layered film is configured such that, after 2 years of use,
the airsole retains an inflation pressure of at least about 70 percent of the initial
inflation pressure, of at least 80 percent of the initial inflation pressure, or of
at least 90 percent of the initial inflation pressure.
[0196] Optionally, the bulbous heel portion does not exhibit visually-observable crazing
after at least 350,000 KIM cycles, or at least 400,000 KIM cycles.
[0197] Optionally, the airsole has a gas transmission rate of no more than 120 percent of
an original gas transmission rate after 320,000 KIM cycles.
[0198] Optionally, the airsole has a gas transmission rate ranging from about 0.5 to about
2 cubic centimeters per square meter per day for nitrogen measured at 23 degrees Celsius
and 0 percent relative humidity for a structure having a thickness ranging from about
72 micrometers to about 320 micrometers after from about 0 KIM cycles to about 320,000
KIM cycles.
[0199] A method of making a bladder that comprises a first sheet and a second sheet, wherein
a first side of the first sheet faces a second side of the second sheet, may comprise:
bonding the first sheet and the second sheet together to form an internal cavity in
a space between the first side of the first sheet and the second side of the second
sheet, wherein the bond extends around at least a portion of a perimeter of the internal
cavity, optionally wherein the bond is contiguous around only one or more portions
of the perimeter of the internal cavity, and includes one or more apertures capable
of admitting a fluid to the internal cavity, forming an open cavity; or wherein the
bond is contiguous around an entire perimeter of the internal cavity, forming a sealed
bladder capable of retaining a fluid in the internal cavity;
wherein the first sheet, the second sheet, or both comprise a multi-layered film as
described herein.
[0200] Optionally, the bladder comprises one or more internal cavities, optionally wherein
the one or more internal cavities includes at least two internal cavities, and optionally
wherein each of the one or more internal cavities is an open cavity, or each of the
one or more internal cavities is a sealed bladder, or the one or more internal cavities
include at least one open cavity and at least one sealed bladder.
[0201] Optionally, bonding comprises adhesively bonding or thermally bonding, optionally
wherein the first sheet and the second sheet include a thermal bond formed by radio
frequency (RF) welding.
[0202] Optionally, the method further comprises closing the one or more apertures in the
perimeter of the internal cavity, thereby forming a sealed bladder.
[0203] Optionally, closing comprises forming an adhesive bond or a thermal bond between
the first side of the first sheet and the second side of the second sheet at the one
or more apertures.
[0204] Optionally, the method further comprises inflating the sealed bladder with a fluid.
[0205] Optionally, the method further comprises subjecting the bladder to a thermoforming
step, optionally wherein the thermoforming step occurs before inflation of the bladder,
or wherein the thermoforming step occurs simultaneously with inflation of the bladder,
or wherein the thermoforming step occurs after inflation of the bladder, or any combination
thereof.
[0206] Optionally, in the method, the bladder comprises an outer surface and thermoforming
comprises placing the bladder in a mold, wherein the mold comprises an inner molding
surface.
[0207] Optionally, the inner molding surface contacts the outer surface of the bladder.
[0208] Optionally, a protective sheath having an outer surface is placed between at least
a portion of the outer surface of the bladder and the inner molding surface, and wherein
the outer surface of the protective sheath contacts the inner molding surface.
[0209] Optionally, the protective sheath comprises an inner surface, wherein the inner surface
of the protective sheath contacts the outer surface of the bladder; optionally wherein
the inner surface of the protective sheath comprises a raised pattern.
[0210] Optionally, the inner surface of the protective sheath comprises a raised pattern
and wherein the raised pattern is imprinted into the bladder during thermoforming.
[0211] Optionally, thermoforming comprises increasing a temperature of the bladder to a
softening temperature of the first sheet, the second sheet, or both, conforming the
outer surface of the bladder to the shape of the inner molding surface.
[0212] Optionally, thermoforming further comprises applying a compressive force between
the outer surface of the bladder and the inner molding surface, or optionally between
the outer surface of the protective sheath and the inner molding surface.
[0213] Optionally, the compressive force provides a pressure differential between the outer
surface of the bladder and the inner molding surface, or optionally between the outer
surface of the protective sheath and the inner molding surface.
[0214] Optionally, the pressure differential is a positive pressure differential.
[0215] Optionally, the pressure differential is a negative pressure differential.
[0216] A method for making an article of footwear disclosed herein may comprise:
securing the bladder disclosed herein to an upper for an article of footwear.
[0217] The method may further comprise securing the bladder disclosed herein to an outsole
and a midsole chassis, such that the bladder is disposed between the midsole chassis
and the outsole to produce a sole structure; and
securing the midsole chassis to an upper for an article of footwear.
BLADDERS AND AIRBAGS
[0218] In the bladder of the article of claim 1, the first film, or the second film, or
each of the first film and the second film is a multi-layered film. Thus, in one aspect,
an airbag can include a first sheet, a second sheet, or both a first sheet and a second
sheet of the multi-layered film that are bonded together (e.g., thermally bonded)
to form an internal cavity in a space between the first and second sheets, where the
bond extends around at least a portion of a perimeter of the internal cavity. The
internal cavity can be inflated with one or more fluids (e.g., one or more gases)
during or after the bonding step. In some aspects, the bond extends around the entire
perimeter of the internal cavity, providing a sealed airbag. In other aspects, the
bond extends around only a portion of the entire perimeter (e.g., around most of the
entire perimeter) and defines a sealable aperture configured to receive fluid(s)/gases(s)
to the internal cavity. Under each aspect, when inflated and sealed, the resulting
airbag is capable of retaining the received fluid(s)/gases(s) in the internal cavity
for extended usage due to the gas-barrier properties of the multi-layered film. In
some aspects, the bladder can comprise a second multi-layered film, optionally wherein
the structure of the second multi-layered film differs from the structure of the first
multi-layered film in number of gas-barrier layers and elastomeric layers, or differs
in thickness of gas-barrier layers and elastomeric layers, or differs in both number
and thickness of gas- barrier layers and elastomeric layers.
[0219] As discussed in more detail below, the multi-layered film includes one or more core
regions, where each of the one or more core regions comprises multiple layers that
alternate between thin gas-barrier layers (each having at least one gas-barrier material)
and elastomeric layers (each having at least one elastomeric material). In an aspect,
in the core region, the gas-barrier material(s) of the gas-barrier layers and the
elastomeric material(s) of the elastomeric layers have similar processing characteristics
and can be co-extruded with reduced interlayer shear. This allows the alternating
gas-barrier layers and elastomeric layers to be co-extended while retaining their
structural integrities and desired layer thicknesses for use in the resulting multi-layered
films.
[0220] In an aspect, to impart good gas-barrier properties, the gas-barrier materials of
the gas-barrier layers are typically less flexible (e.g., more glass-like) than the
elastomeric materials of the elastomeric layers. In particular, the elastomeric materials
of the elastomeric layers may have a lower glass transition temperature than the gas-barrier
materials of the gas-barrier layers, for example 20 degrees Celsius lower, particularly
50 degrees Celsius lower. As such, the gas-barrier layers of the core region(s) are
more susceptible to microscopic cracking when subjected to repeated, excessive stress
loads, such as those potentially generated during flexing and release of the multi-layered
film.
[0221] It has been found that the use of at least 20, or at least 30, or at least 40 gas-barrier
layers, where each gas-barrier layer has an average layer thickness in a range of
from about 0.01 to about 0.75 micrometers (optionally, in a range of from about 0.01
to about 0.5 micrometers), and a corresponding number of elastomeric layers such that
in each core region, the gas-barrier layers and the elastomeric layers alternate,
can increase the flexibility of the core region(s), while maintaining the durability
and gas-barrier properties of the multi-layered film. As such, airbags incorporating
the multi-layered film can be designed to withstand repeated flexing and release (e.g.,
by walking, running, and jumping) with reduced with reduced or no visually observable
cracking, crazing, or hazing over extended usage.
[0222] In an aspect, the multi-layered films and airbags, bladders, and other enclosed and/or
hollow articles constructed therefrom are configured to withstand repeated flexing
and release without cracking, crazing, or developing haze or other significant appearance
changes. In an exemplary aspect, a bladder constructed from sheets comprising the
multi-layered films can be incorporated as a cushioning element into a sole structure
of an article of footwear. Further in this aspect, actions such as walking, running,
and jumping may cause flexing and release of the bladder; however, bladders and other
articles comprising the multi-layered films have a longer useful lifetime than known
cushioning elements. In one aspect, disclosed herein is an article comprising the
disclosed multi-layered films. In one aspect, the article is a cushioning element.
In another aspect, the multi-layered film forms an external-facing layer of the cushioning
element and is effective at retaining a fluid in the cushioning element. In any of
these aspects, the cushioning element is a component of a consumer good such as an
article of footwear, apparel, or sporting equipment. In another aspect, the cushioning
element is a cushioning element for an article of footwear, and the cushioning element
for the article of footwear is an airsole.
[0223] Each of the elastomeric layers has an average thickness of from about 2 micrometers
to about 8 micrometers, such as from about 2 micrometers to about 5 micrometers, from
about 5 micrometers to about 8 micrometers, or from about 4 micrometers to about 6
micrometers.
[0224] In some aspects, the core region comprises at least 50 gas-barrier layers, or from
about 50 to about 100 gas-barrier layers, from about 60 to about 80 gas-barrier layers,
or from about 60 to about 70 gas-barrier layers. In one aspect, the core region comprises
at least 50 elastomeric layers, or from about 50 to about 100 elastomeric layers,
from about 60 to about 80 elastomeric, or from about 60 to about 70 elastomeric layers.
[0225] In one aspect, the average total thickness of the core region ranges from about 125
to about 200 micrometers and the multi-layered film further includes a first structural
layer secured to a first side of the core region, wherein the first structural layer
has an average thickness of from about 900 micrometers to about 1990 micrometers,
optionally from about 900 micrometers to about 1500 micrometers, from about 1500 micrometers
to about 1990 micrometers, or from about 1000 micrometers to about 1400 micrometers;
and a second structural layer secured to a second side of the core region that is
opposite to the first side of the core region, wherein the second structural layer
has an average thickness of from about 900 micrometers to about 1990 micrometers,
optionally from about 900 micrometers to about 1500 micrometers, from about 1500 micrometers
to about 1990 micrometers, or from about 1000 micrometers to about 1400 micrometers.
[0226] In another aspect, the structural layer material of each of the one or more structural
layers independently comprises or consists essentially of a polydiene polyol-based
thermoplastic polyurethane.
[0227] In another aspect, the disclosed bladders further include one or more cap layers
comprising or consisting essentially of a cap layer material. In another aspect, the
cap layer material of the one or more cap layers comprises or consists essentially
of a polyurethane, a polyacrylate, an ethylene-acrylate copolymer, a maleic anhydride
grafted polyolefin, or any combination thereof. In still another aspect, each cap
layer has a thickness of from about 5 micrometers to about 25 micrometers, or from
about 5 micrometers to about 10 micrometers, or from about 10 micrometers to about
20 micrometers.
[0228] In still another aspect, the disclosed bladders further include one or more tie layers,
each of the one or more tie layers comprising or consisting essentially of a tie material,
wherein the one or more tie layers increase a bond strength between two adjacent layers.
In another aspect, the tie material of each of the one or more tie layers independently
comprises or consists essentially of a polyurethane, a polyacrylate, an ethylene-acrylate
copolymer, a maleic anhydride grafted polyolefin, or any combination thereof. In still
another aspect, each of the one or more tie layers has a thickness of from about 5
micrometers to about 20 micrometers, or from about 5 micrometers to about 10 micrometers,
or from about 10 micrometers to about 20 micrometers.
[0229] As used herein, a gas-barrier layer is understood to be a membrane comprising or
consisting essentially of a gas-barrier material, where the thickness of the gas-barrier
material in the gas-barrier layer is at least 0.01 microns. The gas-barrier material
comprises or consists essentially of one or more gas-barrier compounds, including
one or more polymeric gas-barrier compounds (i.e., gas-barrier polymers), or one or
more non-polymeric gas-barrier compounds, or a combination of one or more gas-barrier
polymers and one or more non-polymeric gas-barrier compounds. Polymeric and non-polymeric
gas-barrier compounds have the ability to restrict the passage of gasses through the
material. While no polymer offers an infinite gas-barrier, gas-barrier polymers typically
exhibit higher level of crystallinity at room temperature, and higher levels of intramolecular
hydrogen bonding, as compared with polymers which are poor gas-barriers. Many examples
of gas-barrier polymers and non-polymeric gas-barrier compounds are known in the art.
The one or more gas-barrier compounds can include one or more gas-barrier polymers,
particularly one or more thermoplastic gas-barrier polymers. In the multi-layered
film, one or more gas-barrier layers may be used alone, or in combination with other
layers formed of other materials, including other polymeric materials such as elastomeric
materials. The other layers formed of elastomeric materials are referred to as "elastomeric
layers," and the elastomeric material comprises or consists essentially of one or
more elastomers, particularly one or more thermoplastic elastomers. A "core region"
is an internal region of the multi-layered film in which the one or more gas-barrier
layers are located. In many aspects, the core region comprises a plurality of individual
gas-barrier layers each alternating with a layer formed of other materials. Particularly,
the core region comprises a plurality of gas-barrier layers each having an average
thickness of less than or equal to about 0.75 micrometers, each of the gas-barrier
layers alternating with an elastomeric layer, optionally at least 20 individual gas-barrier
layers each alternating with an elastomeric layer. When used alone or in combination
with other materials (particularly, elastomeric materials) in an airbag or bladder,
the core region resiliently retains the gas. Depending upon the structure and use
of the airbag or bladder, the core region may retain the gas at a pressure which is
above, at, or below atmospheric pressure. Examples of gasses include air, oxygen gas
(O
2), and nitrogen gas (N
2), as well as inert gasses. In one aspect, the gas-barrier layer is a nitrogen gas-barrier
layer.
[0230] The gas transmission rate of the core region of the multi-layered film or of the
entire multi-layered film, such as the oxygen gas or nitrogen gas transmission rate,
can be measured using ASTM D1434. Thus, as used herein, the term "gas-barrier" material
may refer to a material forming one or more layers in a core region of a multi-layered
film, the core region of the multi-layered film having a total thickness less than
or equal to 200 micrometers, or less than or equal to 100 micrometers, in which the
core region, or the multi-layered film as a whole, has an oxygen gas or nitrogen gas
transmission rate as measured using ASTM D1434 of less than or equal to about 4 cubic
centimeters per square meter per day, optionally less than or equal to about 3 cubic
centimeters per square meter per day.
[0231] Optionally, the multi-layered film comprises from about 40 to about 90 layers. In
particular, the multi-layered film comprises about 20 or more gas-barrier layers,
such as about 30 or more gas-barrier layers, or about 40 or more gas-barrier layers,
optionally fewer than 70 gas-barrier layers.
[0232] In one aspect of a multi-layered film, the plurality of layers includes a series
of alternating layers, in which the alternating layers include two or more gas-barrier
layers, each of the two or more gas-barrier layers individually comprising a gas-barrier
material, the gas-barrier material comprising or consisting essentially of one or
more gas-barrier compounds. In the series of alternating layers, adjacent layers are
individually formed of materials which differ from each other at least in their chemical
compositions based on the individual components present (e.g., the materials of adjacent
layers may differ based on whether or not a gas-barrier compound is present, or differ
based on class or type of gas-barrier compound present), the concentration of the
individual components present (e.g., the materials of adjacent layers may differ based
on the concentration of a specific type of gas-barrier compound present), or may differ
based on both the components present and their concentrations.
[0233] The plurality of layers of the multi-layered film can include first gas-barrier layers
comprising a first gas-barrier material and second gas-barrier layers comprising a
second gas-barrier material, wherein the first and second gas-barrier materials differ
from each other based as described above. The first gas-barrier material can be described
as comprising a first gas-barrier component consisting of all the gas-barrier compounds
present in the first gas-barrier material, and the second gas-barrier material can
be described as comprising a second gas-barrier material component consisting of all
the gas-barrier compounds present in the second gas-barrier material. The first gas-barrier
component may consist only of one or more gas-barrier polymers, and the second gas-barrier
component may consist only of one or more inorganic gas-barrier compounds. The first
gas-barrier component may consist of a first one or more gas-barrier polymers, and
the second gas-barrier component may consist of a second one or more gas-barrier polymers,
wherein the first one or more gas-barrier polymers differ from the second one or more
gas-barrier polymers in polymer class, type, or concentration. The first gas-barrier
component and the second gas-barrier component may both include the same type of gas-barrier
compound, but the concentration of the gas-barrier compound may differ, optionally
the concentrations may differ by at least 5 weight percent based on the weight of
the gas-barrier material. In these multi-layered films, the first gas-barrier layers
and the second gas-barrier layers may alternate with each other, or may alternate
with additional gas-barrier layers (e.g., third gas-barrier layers comprising a third
gas-barrier material, fourth gas-barrier layers comprising a fourth gas-barrier material,
etc., wherein each of the first, second, third and fourth, etc., gas-barrier materials
may differ from each other as described above).
[0234] The gas-barrier material comprises or consists essentially of one or more gas-barrier
compounds. The one or more gas-barrier compounds may comprise one or more gas-barrier
polymers, or may comprise one or more non-polymeric gas-barrier compounds, including
one or more inorganic gas-barrier compounds, or may comprise a combination of at least
one gas-barrier polymer and at least one non-polymeric gas-barrier compound. The combination
of at least one gas-barrier polymer and at least one non-polymeric gas-barrier compound,
including at least one inorganic gas-barrier compound, may comprise a blend or mixture,
or may comprise a composite in which fibers, particles, or platelets of the non-polymeric
gas-barrier compound are surrounded by the gas-barrier polymer.
[0235] The gas-barrier material may comprise or consist essentially of one or more inorganic
gas-barrier compounds. The one or more inorganic gas-barrier compounds may take the
form of fibers, particulates, platelets, or combinations thereof. The fibers, particulates,
platelets may comprise or consist essentially of nanoscale fibers, particulates, platelets,
or combinations thereof. Examples of inorganic gas-barrier compounds include carbon
fibers, glass fibers, glass flakes, silicas, silicates, calcium carbonate, clay, mica,
talc, carbon black, particulate graphite, metallic flakes, and combinations thereof.
The inorganic gas-barrier component may comprise or consist essentially of one or
more clays. Examples of suitable clays include bentonite, montmorillonite, kaolinite,
and mixtures thereof. The inorganic gas-barrier component may consist of clay. Optionally,
the gas-barrier material may further comprise one or more additional ingredients,
such as a polymer, processing aid, colorant, or any combination thereof. In aspects
where the gas-barrier material comprises or consists essentially of one or more inorganic
barrier compounds, the gas-barrier material may be described as comprising an inorganic
gas-barrier component consisting of all inorganic gas-barrier compounds present in
the gas-barrier material. When one or more inorganic gas-barrier compounds are included
in the gas-barrier material, the total concentration of the inorganic gas-barrier
component present in the gas-barrier material can be less than 60 weight percent,
or less than 40 weight percent, or less than 20 weight percent of the total composition.
Alternatively, the gas-barrier material may consist essentially of the one or more
inorganic gas-barrier materials.
[0236] The gas-barrier compound may comprise or consist essentially of one or more gas-barrier
polymers. The one or more gas-barrier polymers may include one or more thermoplastic
polymers. The gas-barrier material may comprise or consist essentially of one or more
thermoplastic polymers, meaning that the gas-barrier material comprises or consists
essentially of a plurality of thermoplastic polymers, including thermoplastic polymers
which are not gas-barrier polymers. In another example, the gas-barrier material may
comprise or consist essentially of one or more thermoplastic gas-barrier polymers,
meaning that all the polymers present in the gas-barrier material are thermoplastic
gas-barrier polymers. The gas-barrier material can be described as comprising a polymeric
component consisting of all polymers present in the gas-barrier material. For example,
the polymeric component of the gas-barrier material may consist of a single class
of gas-barrier polymer, such as, for example, one or more polyolefins, or can consist
of a single type of gas-barrier polymer, such as one or more ethylene-vinyl alcohol
copolymers. Optionally, the gas-barrier material may further comprise one or more
non-polymeric additives, such as one or more fillers, processing aids, colorants,
or any combination thereof.
[0237] Many gas-barrier polymers are known in the art. Examples of gas-barrier polymers
include vinyl polymers such as vinylidene chloride polymers, acrylic polymers such
as acrylonitrile polymers, polyamides, epoxy polymers, amine polymers, polyolefins
such as polyethylenes and polypropylenes, copolymers thereof, such as ethylene-vinyl
alcohol copolymers, and mixtures thereof. Examples of thermoplastic gas-barrier polymers
include thermoplastic vinyl homopolymers and copolymers, thermoplastic acrylic homopolymers
and copolymers, thermoplastic amine homopolymers and copolymers, thermoplastic polyolefin
homopolymers and copolymers, and mixtures thereof. The one or more gas-barrier polymers
may comprise or consist essentially of one or more thermoplastic polyethylene copolymers,
such as, for example, one or more thermoplastic ethylene-vinyl alcohol copolymers.
The one or more ethylene-vinyl alcohol copolymers may include from about 28 mole percent
to about 44 mole percent ethylene content, or from about 32 mole percent to about
44 mole percent ethylene content. The one or more gas-barrier polymers may comprise
or consist essentially of one or more polyethyleneimines, polyacrylic acids, polyethyleneoxides,
polyacrylamides, polyamidoamines, or any combination thereof.
[0238] The multi-layered film may further comprise second layers, the one or more second
layers comprising a second material. Optionally, the second material comprises one
or more polymers. Claim 1 requires a multi-layered film including a core region comprising
at least 20 gas-barrier layers and a plurality of elastomeric layers, wherein the
gas-barrier layers alternate with the elastomeric layers.
[0239] Depending upon the class of gas-barrier compounds used and the intended use of the
multi-layered film, the second material may have a higher gas transmittance rate than
the gas-barrier material, meaning that the second material is a poorer gas-barrier
than the gas-barrier material. In some aspects, the one or more second layers act
as substrates for the one or more gas-barrier layers, and may serve to increase the
strength, elasticity, and/or durability of the multi-layered film. Alternatively or
additionally, the one or more second layers may serve to decrease the amount of gas-barrier
material(s) needed, thereby reducing the overall material cost. Even when the second
material has a relatively high gas transmittance rate, the presence of the one or
more second layers, particularly when the one or more second layers are positioned
between one or more barrier layers, may help maintain the overall gas-barrier properties
of the film by increasing the distance between cracks in the gas-barrier layers, thereby
increasing the distance gas molecules must travel between cracks in the barrier layers
in order to pass through the multi-layered film. While small fractures or cracks in
the gas-barrier layers of a multi-layered film may not significantly impact the overall
barrier properties of the film, using thinner gas-barrier layers, or using a larger
number of thinner gas-barrier layers, can avoid or reduce visible cracking, crazing,
or hazing of the multi-layered film. The one or more second layers may include, but
are not limited to, a tie layer located between and promoting adhesion between two
different layers of the multi-layered film, a structural layer providing mechanical
support to the multi-layered film, a bonding layer including a bonding material such
as a hot melt adhesive material to an exterior surface of the multi-layered film,
a cap layer providing protection to an exterior surface of the multi-layered film,
and any combination thereof.
[0240] The second material may be an elastomeric material comprising or consisting essentially
of at least one elastomer. As used herein, the term elastomer may refer to a material
having an elongation at break of greater than 400 percent, determined in accordance
with ASTM D-412-98 at 25 degrees Celsius. Optionally, the term elastomer may refer
to a material that, when formed into a plaque, has a break strength of from 10 to
35 kilogram-force, such as from about 10 to about 25 kilogram-force, from about 10
to about 20 kilogram-force, from about 15 to about 35 kilogram-force, or from about
20 to about 30 kilogram-force. Optionally, the tensile breaking strength or ultimate
strength of an elastomer, if adjusted for cross-sectional area, may be greater than
70 kilogram-force per square centimeter, or greater than 80 kilogram-force per square
centimeter. Optionally, an elastomer, when formed into a plaque, has a strain to break
of from 450 percent to 800 percent, or from 500 to 800 percent, or from 500 to 750
percent, or from 600 to 750 percent, or from 450 to 700 percent. As another option,
an elastomer plaque may have a load at 100 percent strain of from 3 to 8 kilogram-force
per millimeter, or of about 3 to about 7 kilogram-force per millimeter, about 3.5
to about 6.5 kilogram-force per millimeter, or about 4 to about 5 kilogram-force per
millimeter. Optionally, the elastomer plaque has a toughness of from 850 kilogram-millimeters
to 2200 kilogram-millimeters, or of from about 850 kilogram-millimeters to about 2000
kilogram-millimeters, or of from about 900 kilogram-millimeters to about 1750 kilogram-millimeters,
or of from about 1000 kilogram-millimeters to about 1500 kilogram -millimeters, or
of from about 1500 kilogram-millimeters to about 2000 kilogram-millimeters. Optionally,
the elastomer plaque has a stiffness of from about 35 to about 155, or of from about
50 to about 150, or of from about 50 to about 100, or of from about 50 to about 75,
or of from about 60 to about 155, or of from about 80 to about 150. Optionally, the
elastomer plaque has a tear strength of from about 35 to about 80, or of from about
35 to about 75, or of from about 40 to about 60, or of from about 45 to about 50.
Many gas-barrier compounds are brittle and/or relatively inflexible, and so the one
or more gas-barrier layers may be susceptible to cracking when subjected to repeated,
excessive stress loads, such as those potentially generated during flexing and release
of a multi-layered film. Thus, the elastomeric material may have a lower glass transition
temperature than that of the gas-barrier material (when it comprises one or more polymers),
for example 20 degrees Celsius lower, particularly 50 degrees Celsius lower. A multi-layered
film which includes gas-barrier layers alternating with second layers of an elastomeric
material results in a multi-layered film that is better able to withstand repeated
flexing and release while maintaining its gas-barrier properties, as compared to a
film without the elastomeric second layers present.
[0241] In one aspect, the second material comprises or consists essentially of one or more
polymers. As used herein, the one or more polymers present in the second material
are referred to herein as one or more "second polymers" or a "second polymer," as
these polymers are present in the second material. References to "second polymer(s)"
are not intended to indicate that a "first polymer" is present, either in the second
material, or in the multi-layered film as a whole, although, in many aspects, multiple
classes or types of polymers are present. In one aspect, the second material comprises
or consists essentially of one or more thermoplastic polymers. In another aspect,
the second material comprises or consists essentially of one or more elastomeric polymers.
In yet another aspect, the second material comprises or consists essentially of one
or more thermoplastic elastomers. The second material can be described as comprising
a polymeric component consisting of all polymers present in the second material. In
one example, the polymeric component of the second material consists of one or more
elastomers. Optionally, the second material can further comprise one or more non-polymeric
additives, such as fillers, processing aids, and/or colorants.
[0242] Many polymers which are suitable for use in the second material are known in the
art. Exemplary polymers which can be included in the second material (e.g., second
polymers) include polyolefins, polyamides, polycarbonates, polyimines, polyesters,
polyacrylates, polyesters, polyethers, polystyrenes, polyureas, and polyurethanes,
including homopolymers and copolymers thereof (e.g., polyolefin homopolymers, polyolefin
copolymers, etc.), and combinations thereof. In one example, the second material comprises
or consists essentially of one or more polymers chosen from polyolefins, polyamides,
polyesters, polystyrenes, and polyurethanes, including homopolymers and copolymers
thereof, and combinations thereof. In another example, the polymeric component of
the second material consists of one or more thermoplastic polymers, or one or more
elastomers, or one or more thermoplastic elastomers, including thermoplastic vulcanizates.
Alternatively, the one or more second polymers can include one or more thermoset or
thermosettable elastomers, such as, for example, natural rubbers and synthetic rubbers,
including butadiene rubber, isoprene rubber, silicone rubber, and the like.
[0243] Polyolefins are a class of polymers which include monomeric units derived from simple
alkenes, such as ethylene, propylene, and butene. Examples of thermoplastic polyolefins
include polyethylene homopolymers, polypropylene homopolymers, polypropylene copolymers
(including polyethylene-polypropylene copolymers), polybutene, ethylene-octene copolymers,
olefin block copolymers, propylene-butane copolymers, and combinations thereof, including
blends of polyethylene homopolymers and polypropylene homopolymers. Examples of polyolefin
elastomers include polyisobutylene elastomers, poly(alpha-olefin) elastomers, ethylene
propylene elastomers, ethylene propylene diene monomer elastomers, and combinations
thereof.
[0244] Polyamides are a class of polymers which include monomeric units linked by amide
bonds. Naturally-occurring polyamides include proteins such as wool and silk, while
synthetic amides include polymers such as nylons and aramids. The one or more second
polymers can include thermoplastic polyamides such as nylon 6, nylon 6-6, and/or nylon-11,
as well as thermoplastic polyamide copolymers.
[0245] Polyesters are a class of polymers which include monomeric units derived from an
ester functional group, and are commonly made by condensing dibasic acids such as,
for example, terephthalic acid, with one or more polyols. In one example, the second
material can comprise or consist essentially of one or more thermoplastic polyester
elastomers. Examples of polyester polymers include homopolymers such as polyethylene
terephthalate, polybutylene terephthalate, and poly-1,4-cyclohexylene-dimethylene
terephthalate, as well as copolymers such as polyester polyurethanes.
[0246] Styrenic polymers are a class of polymers which include monomeric units derived from
styrene. The one or more second polymers can comprise or consist essentially of styrenic
homopolymers, styrenic random copolymers, styrenic block copolymers, or combinations
thereof. Examples of styrenic polymers include styrenic block copolymers, such as
acrylonitrile butadiene styrene block copolymers, styrene acrylonitrile block copolymers,
styrene ethylene butylene styrene block copolymers, styrene ethylene butadiene styrene
block copolymers, styrene ethylene propylene styrene block copolymers, styrene butadiene
styrene block copolymers, and combinations thereof.
[0247] Polyurethanes are a class of polymers which include monomeric units joined by carbamate
linkages. Polyurethanes are most commonly formed by reacting a polyisocyanate (e.g.,
a diisocyanate or a triisocyanate) with a polyol (e.g., a diol or triol), optionally
in the presence of a chain extender. The monomeric units derived from the polyisocyanate
are often referred to as the hard segments of the polyurethane, while the monomeric
units derived from the polyols are often referred to as the soft segments of the polyurethane.
The hard segments can be derived from aliphatic polyisocyanates, or from organic isocyanates,
or from a mixture of both. The soft segments can be derived from saturated polyols,
or from unsaturated polyols such as polydiene polyols, or from a mixture of both.
When the multi-layered film is to be bonded to natural or synthetic rubber, including
soft segments derived from one or more polydiene polyols can facilitate bonding between
the rubber and the film when the rubber and the film are crosslinked in contact with
each other, such as in a vulcanization process.
[0248] Examples of suitable polyisocyanates from which the hard segments of the polyurethane
can be derived include hexamethylene diisocyanate (HDI), isophorone diisocyanate (IPDI),
butylenediisocyanate (BDI), bisisocyanatocyclohexylmethane (HMDI), 2,2,4-trimethylhexamethylene
diisocyanate (TMDI), bisisocyanatomethylcyclohexane, bisisochanatomethyltricyclodecane,
norbornane diisocyanate (NDI), cyclohexane diisocyanate (CHDI), 4,4'-dicyclohexhylmethane
diisocyanate (H12MDI), diisocyanatododecane, lysine diisocyanate, toluene diisocyanate
(TDI), TDI adducts with trimethylolpropane (TMP), methylene diphenyl diisocyanate
(MDI), xylylene diisocyanate (XDI), tetramethylxylylene diisocyanate (TMXDI), hydrogenated
xylylene diisocyanate (HXDI), naphthalene 1,5-diisocyanate (NDI), 1,5-tetrahydronaphthalene
diisocyanate, para-phenylene diisocyanate (PPDI), 3,3'-dimethyldiphenyl-4,4'-diisocyanate
(DDDI), 4,4'-dibenzyl diisocyanate (DBDI), 4-chloro-1,3-phenylene diisocyanate, and
any combination thereof. In one aspect, the polyurethane comprises or consists essentially
of hard segments derived from toluene diisocyanate (TDI), or from methylene diphenyl
diisocyanate (MDI), or from both.
[0249] The soft segments of the polyurethane can be derived from a wide variety of polyols,
including polyester polyols, polyether polyols, polyester-ether polyols, polycarbonate
polyols, polycaprolactone polyethers, and combinations thereof. In one aspect, the
polyurethane comprises or consist essentially of monomeric units derived from C
4-C
12 polyols, or C
6-C
10 polyols, or Cs or lower polyols, meaning polyols with 4 to 12 carbon molecules, or
with 6 to 10 carbon molecules, or with 8 or fewer carbon molecules in their chemical
structures. In another aspect, the polyurethane comprises or consists essentially
of monomeric units derived from polyester polyols, polyester-ether polyols, polyether
polyols, or any combination thereof. In yet another aspect, the polyurethane comprises
or consists essentially of soft segments derived from polyols or diols having polyester
functional units. The soft segments derived from polyols or diols having polyester
functional units can comprise about 10 to about 50, or about 20 to about 40, or about
30 weight percent of the soft segments present in the polyurethane.
[0250] The multi-layered film can be produced by various means such as co-extrusion, lamination,
layer-by-layer deposition, or the like. When co-extruding one or more barrier layers
alone or with one or more second layers, selecting materials (e.g., a first barrier
material and a second barrier material, or a single barrier material and a second
material) having similar processing characteristics such as melt temperature and melt
flow index, can reduce interlayer shear during the extrusion process, and can allow
the alternating barrier layers and second layers to be co-extruded while retaining
their structural integrities and desired layer thicknesses. In one example, the one
or more barrier materials and, optionally, the second material when used, can be extruded
into separate individual films, which can then be laminated together to form the multi-layered
film.
[0251] The multi-layered film can be produced using a layer-by-layer deposition process.
A substrate, which optionally can comprise a second material or a barrier material,
can be built into a multi-layered film by depositing a plurality of layers onto the
substrate. The layers can include one or more barrier layers (e,g., first barrier
layers, second barrier layers, etc.). Optionally, the layers can include one or more
second layers. The one or more barrier layers and/or second layers can be deposited
by any means known in the art such as, for example, dipping, spraying, coating, or
another method. The one or more barrier layers can be applied using charged solutions
or suspensions, e.g., cationic solutions or suspensions or anionic solutions or suspensions,
including a charged polymer solution or suspension. The one or more barrier layers
can be applied using a series of two or more solutions having opposite charges, e.g.,
by applying a cationic solution, followed by an anionic solution, followed by a cationic
solution, followed by an anionic solution, etc.
[0252] The thickness of an individual barrier layer is in a range of from about 0.01 micrometers
to about 0.75 micrometers thick, preferably in a range of from about 0.01 micrometers
to about 0.5 micrometers thick. The thickness of an individual second layer can range
from about 2 micrometers to about 8 micrometers thick (in particular, each of the
elastomeric layers of the core region as defined in the claims has an average thickness
in a range of from about 2 micrometers to about 8 micrometers), or from about 2 micrometers
to about 4 micrometers thick.
In a further aspect, thickness of the film and/or their individual layers can be measured
by any method known in the art such as, for example, ASTM E252, ASTM D6988, ASTM D8136,
or using light microscopy or electron microscopy.
[0253] In some aspects, the barrier layers, including the multi-layered film, have a Shore
hardness of from about 35A to about 95A, optionally from about 55A to about 90A. In
these aspects, hardness can be measured using ASTM D2240 using the Shore A scale.
[0254] In one aspect, when a co-extrusion process is used to form the barrier layer from
a plurality of alternating barrier layers and second layers, the barrier material
has a melt flow index of from about 5 to about 7 grams per 10 minutes at 190 degrees
Celsius when using a weight of 2.16 kilograms, while the second material has a melt
flow index of from about 20 to about 30 grams per 10 minutes at 190 degrees Celsius
when using a weight of 2.16 kilograms. In a further aspect, the melt flow index of
the barrier material is from about 80 percent to about 120 percent of the melt flow
index of the barrier material per 10 minutes when measured at 190 degrees Celsius
when using a weight of 2.16 kilograms. In any of these aspects, melt flow index can
be measured using ASTM D1238. Alternatively or additionally, the barrier material
or the second material or both have a melting temperature of from about 165 degrees
Celsius to about 183 degrees Celsius, or from about 155 degrees Celsius to about 165
degrees Celsius. In one such example, the barrier material has a melting temperature
of from about 165 degrees Celsius to about 183 degrees Celsius, while the second material
has a melting temperature of from about 155 degrees Celsius to about 165 degrees Celsius.
Further in these aspects, melting temperature can be measured using ASTM D3418.
[0255] In an aspect, the multi-layered film exhibits a low gas-transmission rate such that
airbags incorporating the multi-layered film can be inflated and sealed for extended
use. Such airbags can provide good cushioning and support when incorporated into consumer
products (e.g., as airsoles for footwear). In a further aspect, the level of cushioning
or support does not significantly decrease over an extended period of time once the
airbags are inflated with a gas, due to the low gas transmission rate of the multi-layered
film, which substantially reduces the escape of the inflation gas.
[0256] In one aspect, the airbag internal cavity is inflated to a positive pressure, i.e.,
has an inflation internal pressure above about 15 pounds per square inch (about 100
kilopascals). In further aspects, airbag internal cavity has an inflation internal
pressure ranging from about 17 pounds per square inch (about 117 kilopascals) to about
30 pounds per square inch (about 207 kilopascals). In further aspects, airbag internal
cavity has an inflation internal pressure ranging from about 20 pounds per square
inch (about 138 kilopascals) to about 22 pounds per square inch (about 152 kilopascals).
In one aspect, after 2 years of use, the airbag internal cavity still has an internal
pressure of at least about 60 percent of the inflation internal pressure. In further
aspects, after 2 years of use, the airbag internal cavity still has an internal pressure
of at least about 70 percent of the inflation internal pressure.
[0257] In some aspects, the airbag has a gas transmission rate of no more than 120 percent
of an original gas transmission rate after 320,000 KIM cycles, where KIM cycles are
performed using the KIM Test Protocol defined in the Property Analysis and Characterization
Procedures section included herein. In one aspect, the bladder has a gas transmission
rate ranging from about 0.5 to about 2 cubic centimeters per square meter per day
for nitrogen measured at 23 degrees Celsius and 0 percent relative humidity for a
film having a thickness ranging from 72 micrometers to 320 micrometers after from
0 KIM cycles to 320,000 KIM cycles. In one aspect, the airbag does not exhibit crazing
or cracking after at least 350,000 KIM cycles, or after at least 400,000 KIM cycles.
[0258] In some embodiments, the multi-layered film may also include additional layers on
one or both opposing sides of the core region(s). For instance, the multi-layered
film may include one or more thicker structural layers to increase the structural
integrity and durability of the multi-layered film during use in articles, such as
airsoles for footwear. Additionally or alternatively, the multi-layered film may also
include one or more cap layers to improve abrasion resistance, assist in airbag formation
(e.g., during thermoforming or blow molding), to improve bonding to other article
components, to improve surface properties for printing graphics and indicia, to improve
visual aesthetics and/or tactile properties, water resistance, and the like.
[0259] As shown in
FIGs. 1 and
2, the footwear 1010 is an example article of footwear that incorporates the multi-layered
film of the present disclosure. As shown in
FIG. 1, the article of footwear 1010 can be divided lengthwise into one or more regions
along a longitudinal axis A1010, such as into a forefoot region 1012, a mid-foot region
1014, and a heel region 1016. The forefoot region 1012 can be further described as
including a toe portion corresponding to a portion of the footwear 1010 that surrounds
the phalanges of a wearer's foot when worn, and a ball portion corresponding to a
portion of the footwear 1010 that surrounds the metatarsophalangeal (MTP) joint of
the wearer's foot when worn. The mid-foot region 1014 corresponds with a portion surrounding
an arch area of the wearer's foot when worn, and the heel region 1016 corresponds
with portions of the footwear 1010 surrounding rear portions of the wearer's foot,
including the calcaneus bone, when worn.
[0260] The footwear 1010 can further include an anterior end 1018 associated with a forward-most
location of the forefoot region 1012, and a posterior end 1020 corresponding to a
rearward-most location of the heel region 1016. As further shown in
FIG. 1, the longitudinal axis A1010 of the footwear 1010 extends along the length of the
footwear 1010 from the anterior end 1018 to the posterior end 1020, and generally
divides the footwear 1010 into a medial side 1022 and a lateral side 1024. Accordingly,
the medial side 1022 and the lateral side 1024 respectively correspond with opposite
sides of the footwear 1010 and extend through the regions 1012, 1014, and 1016.
[0261] The footwear 1010 also includes an upper 1026 and a sole structure 1028, where the
upper 1026 forms a structure that is configured to cover some or all of a wearer's
foot and can fit the wearer's foot to the sole structure 1028. The upper 1026 includes
an interior surface (not shown) that defines an interior void configured to receive
and secure a wearer's foot for support on the sole structure 1028. The interior void
can be accessed at an ankle opening 1026a and can be shaped and sized to match and
fit the wearer's foot. For instance, the upper 1026 can extend over the instep and
toe areas of the wearer's foot (at the forefoot region 1012), along medial and lateral
sides of the wearer's foot (at the mid-foot region 1014), and around the heel area
of the wearer's foot (at the heel region 1016).
[0262] The upper 1026 may be formed from one or more components that can be stitched, adhesively
bonded, thermally bonded, or otherwise together to form the interior void, such as
mesh, textiles, foam, leather, and synthetic leather. The materials may be selected
and located to impart properties of durability, air-permeability, wear-resistance,
flexibility, comfort, and the like. More specific examples of suitable materials for
the upper 1026 are discussed below.
[0263] The upper 1026 can also have any suitable design, shape, size, and/or colorway for
footwear applications. For example, in certain aspects, e.g., if the footwear 1010
is a basketball shoe, then the upper 1026 can be a high-top profile that is shaped
to provide high support to a wearer's ankle. Alternatively, in certain aspects, e.g.,
if footwear 1010 is a running shoe, then the upper 1026 can have a low-top profile.
[0264] In the example shown in
FIGs. 1 and
2, the sole structure 1028 includes a midsole 1030 configured to provide cushioning,
support, and aesthetic characteristics, and an outsole 1032 configured to provide
a ground-engaging surface of the footwear 1010. In the shown embodiment, the midsole
1030 of the sole structure 1028 is further divided into multiple subcomponents that
can provide different forms of cushioning, support, and aesthetics, such as a chassis
1034 and an airsole 1036.
[0265] The chassis 1034 can be attached to the upper 1026 to provide an interface between
the upper 1026 and the airsole 1036. In the embodiment illustrated in
FIGs. 1 and
2, the chassis 1034 is a single-component chassis formed from one or more resilient
materials, such as foams and/or rubbers, to impart properties of cushioning, responsiveness,
and energy distribution to the wearer's foot.
[0266] In the shown embodiment, the chassis 1034 is depicted as having a single, full-length
component extending from the forefoot region 1012 to the heel region 1016. Alternatively,
the chassis 1034 may include multiple components, such as a first component extending
from the forefoot region 1012 to the mid-foot region 1014 and a second component extending
from the mid-foot region 1014 to the heel region 1016. In yet further alternative
aspects, the chassis 1034 may include multiple components providing zonal regions
of cushioning and/or rigid support at forefoot region 1012, midfoot region 1014, and/or
heel region 1016. The component(s) of the chassis 1034 may be pre-formed from any
suitable resilient materials (e.g., foams and rubbers) and/or rigid materials (e.g.,
plates and molded parts). In embodiments incorporating resilient materials, the component(s)
of the chassis 1034 can include molded foam parts, loose foam beads retained in carrier
shells, fused foam bead parts (e.g., by compression molding or steam chest molding),
foam beads entrapped in a resilient polymeric resin matrix, and the like to impart
properties of cushioning, responsiveness, support, and energy distribution to the
wearer's foot.
[0267] Examples of suitable resilient materials for foams include thermoplastic elastomers
such as, for example, thermoplastic elastomeric polyolefin homopolymers or copolymers,
thermoplastic elastomeric polyamide homopolymers or copolymers, thermoplastic elastomeric
polyester homopolymers or copolymers, thermoplastic elastomeric polyurethane homopolymers
or copolymers, thermoplastic elastomeric styrenic homopolymers or copolymers, or any
combination thereof. These materials may also include one or more additives, such
blowing agents, cross-linking agents, colorants, fillers, and the like. Suitable chemical
blowing agents include azo compounds such as azodicarbonamide, sodium bicarbonate,
isocyanate, and combinations thereof. Alternatively, the foams of the chassis 1034
may be produced using one or more physical blowing agents that can phase transition
to gases based on a change in temperature and/or pressure. Suitable cross-linking
agents (for cross-linked foams) include peroxide-based crosslinking agents such as
dicumyl peroxide. Suitable fillers include modified or natural clays, modified or
unmodified synthetic clays, talc glass fiber, powdered glass, modified or natural
silica, calcium carbonate, mica, paper, wood chips, and combinations thereof.
[0268] In some embodiments, the chassis 1034 can include one or more semi-rigid plate components,
such as carbon-fiber plates, polymeric (e.g., polyamide-based) plates, and the like.
In further alternative embodiments, the chassis 1034 can be omitted and the airsole
1036 can be directly secured to the upper 1026.
[0269] As shown in
FIGs. 1 and
2, the outsole 1032 can have a geometry that matches the geometry of airsole 1036 and
is configured to provide a ground-engaging surface of the footwear 1010. For example,
the outsole 1032 can be provided as a polymeric component that is overmolded onto,
adhered to, or otherwise secured to the airsole 1036 to provide increased durability,
puncture resistance, and/or abrasion resistance to the airsole 1036 in the ground-facing
direction. Examples of suitable materials for the outsole 1032 include those capable
of bonding to the airsole 1036 directly and/or with adhesives, and that preferably
exhibit abrasion resistance and/or puncture resistance, such as polyurethanes, thermoplastic
polyurethanes, polyether block amines, vulcanized rubbers, and combinations thereof.
[0270] The airsole 1036 is an example airbag for use with the footwear 1010 and incorporates
the multi-layered film of the present disclosure. As briefly noted above, the multi-layered
film exhibits an increased balance between durability and flexibility, while also
retaining good gas-barrier properties. As such, airsoles incorporating the multi-layered
film can have a broader range of unique and advanced three-dimensional geometries
than those achievable with current barrier films.
[0271] For example, the airsole 1036 can include one or more protruding and/or bulbous portions,
such as a heel portion 1038 at the heel region 1016, medial portions 1040a, 1040b,
and 1040c at the medial side 1022, and/or lateral portions 1042a, 1042b, and 1042c
at the lateral side 1024. These protruding portions, particularly heel portion 1038,
can potentially be subjected to high stress loads from flexing and release during
each foot strike due to their extreme geometries, potentially resulting in significant
flexing deformation of the multi-layered film and the barrier layers within. This
is best illustrated in
FIG. 3, which shows the portions 1038; 1040a, 1040b, and 1040c; and 1042a, 1042b, and 1042c
of the airsole 1036 extending beyond a top-down, cross-sectional footprint of the
chassis 1034 of the midsole 1030. As can be appreciated, during each foot strike,
the downward pressure applied to the airsole 1036 by the wearer's body weight and
transferred through the upper 1026 and the chassis 1034 can generate high stress loads
on the protruding portions 1038; 1040a, 1040b, and 1040c; and 1042a, 1042b, and 1042c.
These high stress loads resulting from flexing and release of the multi-layered film
can be particularly high at the heel portion 1038 due to heel-striking during walking
and running. Furthermore, these high stress loads are compounded over time through
repeated flexing and release of the multi-layered film of the airsole 1036, which
can occur with each foot strike.
[0272] The effects of flexing and release of the multi-layered film are illustrated in
FIGs.
4A and
4B. FIG. 4A is an expanded view of the heel portion 1038 at the heel region 1016 in an uncompressed
state, such as when the footwear 1010 raised during a walking or running stride or
when the footwear 1010 is sitting on an underlying surface (e.g., surface 1044) without
any applied weight.
[0273] Still referring to
FIGs. 4A and
4B, heel portion 1038 is a bulbous, protruding portion having a height 1046 in an uncompressed
state, where the height 1046 is distance from the top of the airsole 1036 at the chassis
1034 to the bottom of the airsole 1036 at the outsole 1032 as taken along an axis
1048 that is a vertical axis perpendicular to the surface 1044 when the footwear 1010
is resting upright on the surface 1044. In an exemplary aspect, suitable heights 1046
can range from about 10 to about 24 millimeters, from about 10 to 20 millimeters,
or from about 15 to about 24 millimeters. Heel portion 1038 further protrudes rearwardly
from the chassis 1034 by a distance 1050 in a direction along or parallel to axis
A1010.
[0274] In one aspect, a point 1052 can be defined as a furthest rearward point on heel portion
1038 along axis A1010. As shown in
FIG. 4A, the extent of the bulbous, protruding geometry of the heel portion 1038 can be defined
by two vectors. These two vectors include a first vector 1054, which begins at point
1052 and extends through a rearward-most contact point 1056 between the chassis 1034
and the airsole 1036, and a second vector 1058 begins at point 1052 and extends through
a rearward-most contact point 1060 between the outsole 1032 and the airsole 1036.
In some aspects, an angle 1062 between the first vector 1054 through point 1056 and
the second vector 1058 through point 1060 ranges from about 115 degrees to about 137.5
degrees, or from about 115 degrees to about 125 degrees, or from about 120 degrees
to about 137.5 degrees.
[0275] As can be appreciated, the bulbous, protruding geometry of the heel portion 1038,
as can be independently characterized by the height 1046, the rearward distance 1050,
and the angle 1062 is vertically unsupported by either outsole 1032 or chassis 1034.
As also can be appreciated, a greater rearward distance 1050 will subject the multi-layered
film of the airsole 1036 at the location of point 1052 to greater the potential stress
loads during each foot strike. Accordingly, examples of suitable distances 1050 can
range from about 4.5 millimeters to about 7.1 millimeters, or from about 4.5 millimeters
to about 6.0 millimeters, or from about 6.0 millimeters to about 7.1 millimeters.
[0276] FIG. 4B is an expanded view of the heel portion 1038 in a compressed state, such as when
the footwear 1010 is receiving a load applied by a wearer's foot strike on the surface
1044. In one aspect, in the compressed state, the heel portion 1038 has a reduced
height 1064, where height 1064 is a distance from the top of the airsole 1036 at the
chassis 1034 to the bottom of the airsole 1036 at the outsole 1032, as taken along
the axis 1048. Examples of suitable heights 1064 range from about 8.6 to about 13.6
millimeters, or from about 8.6 to about 11 millimeters, or from about 10 millimeters
to about 13.6 millimeters. Further in this aspect, the heel portion 1038 protrudes
rearwardly by a distance 1066 taken in direction along or parallel to the axis A1010.
Examples of suitable distances 1066 range from about 6.4 millimeters to about 8.2
millimeters, or from about 6.4 millimeters to about 7.0 millimeters, or from about
7.0 millimeters to about 8.2 millimeters.
[0277] In one aspect, in a compressed state, a 200 pound weight is placed on the disclosed
bladder and/or an article of footwear comprising the bladder. In an alternative aspect,
in a compressed state, the bladder and/or article of footwear is subjected to an applied
force equivalent to that exerted by a 300 pound person wearing a pair of footwear
including the bladders in a sole structure thereof.
[0278] As shown in
FIGs. 4A and
4B, the height 1046 in the uncompressed state is greater than the height 1064 in the
compressed state. Examples of suitable differences in heights 1046 and 1064 range
from about 1.4 millimeters to about 10.4 millimeters, as measured by the Load Compression
Test Protocol described in the Property Analysis and Characterization Procedures section
herein. In another aspect, the height 1064 in the compressed state ranges from about
56.7 percent to about 86.0 percent of the height 1046 in the uncompressed state, as
measured by the Load Compression Test Protocol. In a further aspect, the differences
between the uncompressed height 1046 and the compressed height 1064 are applicable
at the time of manufacturing as well as within 3 months of use, within 6 months of
use, within 1 year of use, or within 2 years of use. Without wishing to be bound by
theory, an inflated airsole that does not exhibit crazing or cracking after at least
320,000 KIM cycles or greater retains a low gas transmission rate and a high proportion
of its inflation internal pressure, thus limiting the amount of compression possible
and thus limiting compressed height 1064 as a proportion of uncompressed height 1046
after a period of regular use.
[0279] As can also be appreciated, the distance 1050 in the uncompressed state is less than
the distance 1066 in the compressed state. Examples of suitable differences in the
distances 1050 and 1066 range from about 1.1 millimeters to about 1.9 millimeters,
as measured by the Load Compression Test Protocol. In a further aspect, the suitable
differences in distances are applicable at time of manufacturing, within 3 months
of use, within 6 months of use, within 1 year of use, or within 2 years of use. In
another aspect, distance 1050 in the uncompressed state ranges from about 70.3 percent
to about 86.6 percent of the distance 1066 in the compressed state, as measured by
the Load Compression Test Protocol.
[0280] As shown, a point 1068 is furthest rearward point on heel portion 1038 along axis
A1010 when the airsole is in the compressed state, while the point 1052 is the furthest
rearward point on heel portion 1038 along axis A1010 when the airsole is in the uncompressed
state. In some aspects, point 1068 and point 1052 are located on the same physical
location of the heel portion 1038, while in other aspects, such as when the airsole
1036 has an asymmetrical shape and/or bend location, point 1068 and point 1052 can
be located on different physical spots of the heel portion 1038.
[0281] The extent of the compression of the bulbous, protruding geometry of the heel portion
1038 can be defined by two vectors. These two vectors include a first vector 1070
that begins at point 1068 and extends through a rearward-most contact point 1056 between
the chassis 1034 and the airsole 1036, while a second vector 1072 begins at point
1068 and extends through a rearward-most contact point 1060 between the outsole 1032
and the airsole 1036. Still further in this aspect, the angle 1074 between the first
vector 1070 and the second vector 1072 ranges from about 38 degrees to about 107 degrees,
or from about 38 degrees to about 80 degrees, or from about 80 degrees to about 107
degrees. As can be appreciated, the bulbous, protruding geometry of the heel portion
1038, as can be independently characterized by the height 1064, the rearward distance
1066, and the angle 1074 is vertically unsupported by either outsole 1032 or chassis
1034. As also can be appreciated, a greater rearward distance 1066 will subject the
multi-layered film of the airsole 1036 at the location of point 1068 to greater potential
stress loads during each foot strike. Accordingly, examples of suitable distances
1066 can range from about 6.4 millimeters to about 8.2 millimeters, or from about
6.4 millimeters to about 7.0 millimeters, or from about 7.0 millimeters to about 8.2
millimeters.
[0282] In any of these aspects, the angle 1074 in the compressed state is less than the
angle 1062 in the uncompressed state. Examples of suitable differences in the angles
1062 and 1074 range from about 37.5 degrees to about 77 degrees, as measured by the
Load Compression Test Protocol. Furthermore, the suitable differences in angles are
applicable at time of manufacturing, within 3 months of use, within 6 months of use,
within 1 year of use, or within 2 years of use. In another aspect, angle 1074 ranges
from about 33.0 percent to about 77.8 percent of angle 1062, as measured by the Load
Compression Test Protocol.
[0283] Although the airsole 1036 depicted in
FIGs. 4A and
4B is depicted symmetrically, in some aspects, the profile or shape of the airsole 1036
can be different from that depicted. In one aspect, the airsole 1036 can be made from
two multi-layered films as disclosed herein, wherein the multi-layered films are sheets
that are joined together around a perimeter. In an aspect, one sheet can be thermoformed
and can, in some aspects, form the bottom of the airsole 1036 in partially in contact
with the outsole 1032. Further in this aspect, a second sheet can form the top of
the airsole 1036, wherein the second sheet may or may not be thermoformed and wherein
the second sheet can be partially on contact with chassis 1034. In any of these aspects,
stress loads caused by flexing and release of the multi-layered film(s) at the heel
portion 1038 may not be distributed symmetrically about an exemplary asymmetric airsole
1036 depending on its particular geometry. For purposes of determining the distance
1050, the vectors 1070 and 1072, and the angle 1074, the longitudinal axis A1010 is
parallel to the surface 1044 as the footwear 1010 is oriented upright on the surface
1044 (e.g., axis A1010 is oriented horizontally in the illustration of
FIGs. 4A and 4B).
[0284] In any of the above aspects, flexing and release stress loads applied to the multi-layered
film of the airsole 1036 can exceed the performance tolerances of currently-known
barrier films over repeated foot strikes in footwear applications, which can produce
visible crazing or hazing effects in the barrier films. While these crazing and hazing
effects do not noticeably affect the performance of the barrier films (e.g., gas retention),
they can detract from the aesthetics of the airsoles, which may be an undesirable
effect for many consumers. The multi-layered film of the present disclosure, however,
can withstand higher repeated stress loads compared to current barrier films used
in footwear applications while exhibiting reduced or no visually observable cracking,
crazing, or hazing and, further, retaining good gas-barrier properties. The gas-barrier
layers of the core region(s) in the disclosed multi-layered film have an average layer
thickness in a range of from about 0.01 micrometers to about 0.75 micrometers, particularly
in a range of from about 0.01 micrometers to about 0.5 micrometers; and have increased
flexibility and/or elastic properties compared to currently-known barrier films, allowing
the multi-layered film of the present disclosure to undergo repeated flexing-release
cycles substantially without losing gas-barrier properties and without the appearance
of crazing, hazing, or the like. Further in this aspect, these superior properties
allow for the disclosed airsoles 1036 to have a longer useful lifetime without an
appreciable change in gas transmission rate.
[0285] Furthermore, while particularly beneficial for use with airbags having more extreme
geometries (e.g., airsole 1036 with uncompressed height 1046), the multi-layered film
of the present disclosure can be used as a suitable replacement in any current gas-barrier
applications that incorporate multi-layered films (e.g., microlayer films). For example,
in footwear applications, the multi-layered film can be incorporated into airsoles
having any suitable geometry, such as those disclosed in
U.S. Patent Nos. 10,149,513,
11,019,880, and
11,019,881 and
U.S. Patent Application Publication Nos. 2019/0231027,
2020/0205514,
2021/0145119, and
2021/0195996. This allows the same multi-layered film to be interchangeably used as feedstock
for multiple different airsole geometries, thereby increasing manufacturing efficiency,
reducing raw material waste, and reducing manufacturing carbon impact.
[0286] As shown in
FIG. 5, multi-layered film 1076 is an example multi-layered film of the present disclosure,
such as for use in the airsole 1036. In some aspects, the articles disclosed herein
can comprise multiple layers as illustrated, for example, in
FIG. 5. In this exemplary embodiment, the article is a sheet comprising gas-barrier layers
and includes two structural layers, 2200a having a thickness 2180a and 2200b having
a thickness 2180b and a core region or film 2160 having a thickness 2140. In one aspect,
the article can be two-sided. Further in this aspect, a two-sided article can include
a symmetrical arrangement of layers on both sides of core region 2160. Suitable examples
of thicknesses 2180a and 2180b range from about 900 micrometers to about 1990 micrometers,
or from about 900 micrometers to about 1400 micrometers, or from about 1400 micrometers
to about 1990 micrometers. Suitable examples of thickness 2140 range from about 125
micrometers to about 200 micrometers, or from about 125 micrometers to about 175 micrometers,
or from about 150 micrometers to about 200 micrometers.
[0287] In one such aspect in accordance with the example of
FIG. 5, structural layers 2200a and 2200b can comprise or consist essentially of a structural
layer material. In such an aspect, the core region 2160 can comprise or consist essentially
of a multi-layered film comprising gas-barrier layers as disclosed herein.
[0288] In any of these aspects, structural layer 2200a can have a first surface 2200a' and
a second surface 2200a", while structural layer 2200b can have a first surface 2200b'
and a second surface 2200b". In another aspect, the core region 2160 can have a first
surface 2160a and a second surface 2160b. In some aspects, the second surface 2200a"
of the structural layer 2200a and the first surface 2160a of the core region 2160
can be adjacent to one another or otherwise in contact with one another. In one aspect,
the second surface 2160b of the core region 2160 and the second surface 2200b" of
the structural layer 2200b can be adjacent to one another or otherwise in contact
with one another. In some aspects, first surface 2200a' of structural layer 2200a
and/or first surface 2200b' of structural layer 2200b can independently optionally
be an outer surface of an article incorporating the multi-layered film disclosed herein.
In any of these aspects, structural layer 2200a and structural layer 2200 can be made
from the same material or from different materials and can have the same or different
thicknesses.
[0289] In one aspect, provided herein are articles comprising the multi-layered films disclosed
herein, the articles including:
a first cap layer comprising or consisting essentially of a first cap layer material,
the first cap layer including a first cap layer outer surface defining a first outer
surface of the multi-layered film, a first cap inner layer surface opposing the first
cap layer outer surface, a first cap layer thickness extending from the first cap
layer inner surface to the first cap layer outer surface, wherein the first cap layer
outer surface defines a first exterior surface of the article;
a second cap layer comprising or consisting essentially of a second cap layer material,
the second cap layer including a second cap layer outer surface defining a second
outer surface of the multi-layered film, a second cap layer inner surface opposing
the second cap layer outer surface, a second cap layer thickness extending from the
second cap layer inner surface to the second cap layer outer surface, optionally wherein
the second cap layer outer surface defines a second exterior surface of the article;
and
one or more core regions as disclosed herein.
[0290] In another aspect, the first cap layer material and the second cap layer material
are substantially the same. In an alternative aspect, the first cap layer material
and the second cap layer material are different. In some aspects, the first cap layer
inner surface is in contact with the core region first surface, or the second cap
layer inner surface is in contact with the core region second surface, or both.
[0291] In one aspect, the gas-barrier material comprises or consists essentially of a nitrogen
barrier material. In a further aspect, the gas-barrier material comprises or consists
essentially of one or more gas-barrier polymers. Further in this aspect, the gas-barrier
material can comprise a gas-barrier polymeric component consisting of all polymers
present in the gas-barrier material. In another aspect, the one or more gas-barrier
polymers comprise or consist essentially of one or more thermoplastic vinylidene chloride
polymers, one or more thermoplastic acrylonitrile polymers or copolymers, one or more
thermoplastic polyamides, one or more thermoplastic epoxy resins, one or more thermoplastic
amine polymers or copolymers, or one or more thermoplastic polyolefin homopolymers
or copolymers. In one aspect, the one or more thermoplastic polyolefin homopolymers
or copolymers comprise or consist essentially of one or more thermoplastic polyethylene
copolymers, or comprise or consist essentially of one or more thermoplastic ethylene-vinyl
alcohol copolymers. In one aspect, the one or more ethylene-vinyl alcohol copolymers
include from about 28 mole percent to about 44 mole percent ethylene content, or from
about 32 mole percent to about 44 mole percent ethylene content.
[0292] In another aspect, the elastomeric material comprises or consists essentially of
one or more thermoplastic elastomeric polymers, and further comprises an elastomeric
polymeric component consisting of all polymers present in the elastomeric material.
In another aspect, the one or more thermoplastic elastomeric polymers comprise or
consist essentially of one or more thermoplastic elastomeric polyolefin homopolymers
or copolymers, one or more thermoplastic elastomeric polyamide homopolymers or copolymers,
one or more thermoplastic elastomeric polyester homopolymers or copolymers, one or
more thermoplastic elastomeric polyurethane homopolymers or copolymers, one or more
thermoplastic elastomeric styrenic homopolymers or copolymers, or any combination
thereof.
[0293] In further aspects, the one or more styrenic homopolymers or copolymers can include
one or more styrenic block copolymers, such as acrylonitrile butadiene styrene block
copolymers, styrene acrylonitrile block copolymers, styrene ethylene butylene styrene
block copolymers, styrene ethylene butadiene styrene block copolymers, styrene ethylene
propylene styrene block copolymers, styrene butadiene styrene block copolymers, and
combinations thereof.
[0294] In an aspect, the elastomeric material comprises or consists essentially of one or
more thermoplastic elastomeric polyurethane homopolymers or copolymers, optionally
wherein the elastomeric material comprises or consists essentially of one or more
polydiene polyol-based thermoplastic elastomeric polyurethane homopolymers or copolymers.
[0295] In some aspects, the one or more thermoplastic elastomeric polyurethane homopolymers
or copolymers comprise a plurality of first segments derived from one or more polyols
and a plurality of segments derived from a diisocyanate. In another aspect, the one
or more thermoplastic elastomeric polyurethane homopolymers or copolymers is a polymerization
product of a diisocyanate with one or more polyols.
[0296] In another aspect, the thermoplastic elastomeric polyurethane homopolymer or copolymer
comprises or consists essentially of one or more polydiene polyol-based thermoplastic
elastomeric polyurethane homopolymers or copolymers, wherein the polyol comprises
or consists essentially of a polybutadiene polyol, a polyisoprene polyol, a partially
or fully hydrogenated derivative of a polybutadiene polyol or of a polyisoprene polyol,
or any combination thereof.
[0297] In another aspect, the one or more polyols comprise or consist essentially of a polyester
polyol, a polyether polyol, a polycarbonate polyol, a polycaprolactone polyether,
or any combination thereof.
[0298] In still another aspect, the diisocyanate comprises or consists essentially of an
aliphatic diisocyanate, an aromatic diisocyanate, or any combination thereof. In one
aspect, the aliphatic diisocyanate comprises or consists essentially of hexamethylene
diisocyanate (HDI), isophorone diisocyanate (IPDI), butylenediisocyanate (BDI), bisisocyanatocyclohexylmethane
(HMDI), 2,2,4-trimethylhexamethylene diisocyanate (TMDI), bisisocyanatomethylcyclohexane,
bisisochanatomethyltricyclodecane, norbornane diisocyanate (NDI), cyclohexane diisocyanate
(CHDI), 4,4'-dicyclohexhylmethane diisocyanate (H12MDI), diisocyanatododecane, lysine
diisocyanate, or any combination thereof. In another aspect, the aromatic diisocyanate
comprises or consists essentially of toluene diisocyanate (TDI), TDI adducts with
trimethylolpropane (TMP), methylene diphenyl diisocyanate (MDI), xylene diisocyanate
(XDI), tetramethylxylylene diisocyanate (TMXDI), hydrogenated xylene diisocyanate
(HXDI), naphthalene 1,5-diisocyanate (NDI), 1,5-tetrahydronaphthalene diisocyanate,
para-phenylene diisocyanate (PPDI), 3,3'-dimethyldiphenyl-4,4'-diisocyanate (DDDI),
4,4'-dibenzyl diisocyanate (DBDI), 4-chloro-1,3-phenylene diisocyanate, or any combination
thereof.
[0299] In an aspect, in the multi-layered films, the gas-barrier material can have a melt
flow index of from about 5 to about 7 grams per 10 minutes at 190 degrees Celsius
when using a weight of 2.16 kilograms. In another aspect, the elastomeric material
can have a melt flow index of from about 20 to about 30 grams per 10 minutes at 190
degrees Celsius when using a weight of 2.16 kilograms. In any of these aspects, in
the multi-layered films, the melt flow index of the gas-barrier material can be from
about 80 percent to about 120 percent of the melt flow index of the elastomeric material,
or from about 90 percent to about 110 percent of the melt flow index of the elastomeric
material, from about 95 percent to about 105 percent of the melt flow index of the
elastomeric material, or can be substantially the same as the melt flow index of the
elastomeric material, when the melt flow index is measured in cubic centimeters per
10 minutes at 190 degrees Celsius when using a weight of 2.16 kilograms.
[0300] In one aspect, the gas-barrier material can have a melting temperature of from about
165 degrees Celsius to about 183 degrees Celsius, while in another aspect, the elastomeric
material can have a melting temperature of from about 155 degrees Celsius to about
165 degrees Celsius. In any of these aspects, the melting temperature of the gas-barrier
material is within about 10 degrees Celsius of the melting temperature of the elastomeric
material, optionally within about 8 degrees Celsius of the melting temperature of
the elastomeric material, or within about 5 degrees Celsius of the melting temperature
of the elastomeric material.
[0301] In any of these aspects, without wishing to be bound by theory, thin gas-barrier
layers alternating with elastomeric layers as disclosed herein can improve the flexibility
tolerances of the core region or multi-layered film without compromising durability
or gas-barrier properties. Further in this aspect, the disclosed multi-layered films
allow for the production of articles incorporating the multi-layered films, wherein
the articles can incorporate extreme geometries without exhibiting cracking, crazing,
hazing, or loss of gas-barrier properties over time.
[0302] In some aspects, the multi-layered films disclosed herein further comprise a blended
material, wherein the blended material comprises or consists essentially of a blend
of one or more additional thermoplastic elastomers and a second material, optionally
wherein the second material comprises or consists essentially of one or more second
polymers, optionally wherein the one or more second polymers comprise or consist essentially
of one or more second thermoplastics.
[0303] In an aspect, the one or more second thermoplastics can comprise one or more thermoplastic
polyolefin homopolymers, one or more thermoplastic polyamide homopolymers or copolymers,
one or more thermoplastic polyester homopolymers or copolymers, one or more thermoplastic
polyurethane homopolymers or copolymers, one or more thermoplastic styrenic homopolymers
or copolymers, or any combination thereof.
[0304] In further aspects, the one or more styrenic homopolymers or copolymers can include
one or more styrenic block copolymers, such as acrylonitrile butadiene styrene block
copolymers, styrene acrylonitrile block copolymers, styrene ethylene butylene styrene
block copolymers, styrene ethylene butadiene styrene block copolymers, styrene ethylene
propylene styrene block copolymers, styrene butadiene styrene block copolymers, and
combinations thereof.
[0305] In another aspect, the one or more second thermoplastics can comprise or consist
essentially of thermoplastic polypropylene homopolymers or copolymers, thermoplastic
polyethylene homopolymers or copolymers, thermoplastic polybutylene homopolymers or
copolymers, or any combination thereof.
[0306] In some aspects, the one or more second thermoplastics comprise or consist essentially
of one or more thermoplastic polyethylene copolymers. In another aspect, the one or
more second thermoplastics comprise or consist essentially of one or more thermoplastic
ethylene-vinyl alcohol copolymers. In one aspect, a polymeric component of the blended
material consists of one or more additional thermoplastic elastomeric polyurethane
homopolymers or copolymers, and one or more second thermoplastic ethylene-vinyl alcohol
copolymers. In an alternative aspect, the polymeric component of the thermoplastic
elastomeric material consists of one or more additional thermoplastic elastomeric
polyester-polyurethane copolymers and one or more second thermoplastic ethylene-vinyl
alcohol copolymers. In some aspects, the blended material comprises one or more recycled
additional thermoplastic elastomers, or one or more recycled second thermoplastics,
or both.
[0307] In some aspects, the blended material is a phase-separated blend of the one or more
additional thermoplastic elastomers and the one or more second thermoplastics. In
some aspects, the phase-separated blend includes one or more phase-separated regions
including interfaces between the one or more additional thermoplastic elastomers and
the one or more second thermoplastics. In some aspects, the blend comprises about
95 percent by weight of the one or more second thermoplastics and about 5 percent
by weight of the one or more second thermoplastics based on a total weight of the
blend.
[0308] As used herein, the term recycled material may refer to a polymeric material which
has previously been extruded into a film, and may have been previously thermoformed
into a bladder, before being shredded or ground and re-extruded into a film. Optionally,
therefore, the thermal history of a material may provide evidence that it is a recycled
material, rather than a virgin material. Optionally, a recycled material, particularly
a recycled polymeric material, may comprise up to 10 percent of a gas-barrier polymeric
material on a weight basis, as it may have been recycled by grinding or shredding
a multi-layered film that included a gas-barrier material. In an aspect, the disclosed
multi-layered films further comprise a recycled material comprising one or more recycled
polymers, optionally wherein the one or more recycled polymers comprise one or more
recycled thermoplastics, optionally wherein the one or more recycled thermoplastics
comprise one or more recycled thermoplastic elastomers; optionally wherein the recycled
material comprises a recycled material polymeric component consisting of one or more
recycled thermoplastics, optionally wherein the recycled material polymeric component
comprises or consists essentially of one or more recycled thermoplastic elastomers.
[0309] In another aspect, the recycled material can comprise one or more recycled thermoplastic
elastomers, and optionally the one or more recycled thermoplastic elastomers comprise
one or more reground thermoplastic elastomers, optionally wherein the one or more
recycled or reground thermoplastic elastomers includes a thermoplastic elastomeric
material as disclosed herein.
[0310] In some aspects, the recycled material further comprises one or more recycled second
thermoplastics, and the one or more recycled second thermoplastics optionally comprise
one or more reground second thermoplastics, optionally wherein the one or more recycled
or reground second thermoplastics include a thermoplastic as disclosed herein.
[0311] In one aspect, the recycled material comprises one or more recycled or reground thermoplastic
polyurethane elastomers or one or more recycled or reground thermoplastic ethylene-vinyl
alcohol copolymers or both. In an aspect, the recycled material comprises a blend
of the one or more recycled or reground thermoplastic elastomers and one or more second
thermoplastics, or comprises a blend of one or more thermoplastic elastomers and one
or more recycled thermoplastics or one or more recycled thermoplastics, optionally
wherein the blend is a phase-separated blend, and optionally wherein the phase-separated
blend comprises one or more interfaces between the one or more recycled thermoplastic
elastomers and the one or more second thermoplastics.
[0312] In another aspect, in the multi-layered films, the recycled material comprises about
99 percent to about 90 percent by weight of the one or more recycled thermoplastic
elastomers and about 1 percent to about 10 percent by weight of the one or more second
thermoplastics based on a total weight of the recycled material, optionally wherein
the recycled material comprises about 99 percent to about 93 percent by weight of
the one or more recycled thermoplastic elastomers and about 1 percent to about 7 percent
by weight of the one or more second thermoplastics, or about 99 percent to about 95
percent by weight of the one or more recycled thermoplastic elastomers and about 1
percent to about 5 percent by weight of the one or more second thermoplastic elastomers.
[0313] In an aspect, the recycled material comprises about 99 percent to about 50 percent
by weight of recycled or reground polymers based on a total weight of recycled material,
or from about 99 percent to about 75 percent by weight of recycled or reground polymers.
[0314] In some aspects, the recycled material further comprises one or more virgin first
thermoplastic elastomers, optionally wherein the one or more virgin thermoplastic
elastomers includes one or more virgin thermoplastic polyurethane elastomers.
[0315] In one aspect, the multi-layered film further comprises one or more tie layers, each
of the one or more tie layers individually comprising or consisting essentially of
a tie material, wherein the one or more tie layers increase a bond strength between
two adjacent layers. In some aspects, the tie material of each of the one or more
tie layers independently comprises or consists essentially of a polyurethane, a polyacrylate,
an ethylene-acrylate copolymer, a maleic anhydride grafted polyolefin, or any combination
thereof, and optionally the tie material comprises or consists essentially of a blended
material or a recycled material as disclosed herein. In another aspect, the tie layer
material of the one or more tie layers independently comprises or consists essentially
of one or more thermoplastic polyurethane elastomeric homopolymers or copolymers,
optionally wherein the one or more tie layers comprise or consist essentially of polydiene
polyol-based thermoplastic polyurethane.
[0316] In one aspect, in the multi-layered films, the elastomeric material can be a first
elastomeric material, and the multi-layered films further include a second elastomeric
material, and the formed multi-layered film further comprises a first structural layer
secured to a first side of one of the one or more core regions, wherein the first
structural layer comprises the second elastomeric material and has an average thickness
ranging from about 900 micrometers to about 1990 micrometers, optionally from about
900 to about 1500 micrometers, from about 1500 to about 1990 micrometers, from about
1200 to about 1800 micrometers, or from about 1000 to about 1400 micrometers.
[0317] In another aspect, the multi-layered films further comprise one or more structural
layers, each of the one or more structural layers independently comprising or consisting
essentially of a structural layer material, optionally wherein the structural layer
material comprises or consists essentially of a blended material or a recycled material
as described herein. In some aspects, the structural layer material of the one or
more structural layers independently comprises or consists essentially of a polydiene
polyol-based thermoplastic polyurethane.
[0318] In still another aspect, the multi-layered films can comprise one or more cap layers,
wherein the one or more cap layers comprise or consist essentially of a cap layer
material, optionally wherein the cap layer material comprises or consists essentially
of a blended material or a recycled material as disclosed herein. In some aspects,
the cap layer material of the one or more cap layers comprises or consists essentially
of a polyurethane, a polyacrylate, an ethylene-acrylate copolymer, a maleic anhydride
grafted polyolefin, or any combination thereof. In another aspect, the cap layer material
of the one or more cap layers comprises or consists essentially of a thermoplastic
polyurethane, optionally a polydiene polyol-based thermoplastic polyurethane.
[0319] In some aspects, at least one of the one or more tie layers is positioned between
one of the one or more structural layers and one of the one or more core regions.
In another aspect, at least one of the one or more structural layers is positioned
between one of the one or more tie layers and one of the one or more cap layers. In
another aspect, the multi-layered film can be a coextruded layered sheet or a laminated
layered sheet.
[0320] In one aspect, disclosed herein is a multi-layered film comprising a first cap layer,
a first structural layer, a first tie layer, a core region, a second tie layer, a
second structural layer, and a second cap layer, wherein a first cap layer inner surface
contacts a first surface of the first structural layer, a second surface of the first
structural layer contacts a first surface of the first tie layer, a second surface
of the first tie layer contacts a first surface of the core region, a second surface
of the core region contacts a first surface of the second tie layer, a second surface
of the second tie layer contacts a first surface of the second structural layer, and
a second surface of the second structural layer contacts an inner layer of the second
cap layer.
[0321] In an alternative aspect, the disclosed multi-layered films have a structure of A-B-C-B-A,
wherein A represents a structural layer, B represents a tie layer, and C represents
a core region. In another aspect, the disclosed multi-layered films have a structure
of D-A-B-C-B-A-D, wherein A represents a structural layer, B represents a tie layer,
C represents a core region, and D represents a cap layer.
[0322] In an aspect, in any of the disclosed multi-layered films, each of the one or more
core regions can have a gas transmission rate of from about 0.3 to about 1.9 cubic
centimeters per square meter per day for nitrogen measured at 23 degrees Celsius and
0 percent relative humidity, optionally for a structure having a thickness of from
about 72 micrometers to about 320 micrometers, optionally wherein each of the one
or more core regions can have a gas transmission rate of from about 0.3 to about 1.9
cubic centimeters per square meter per day for nitrogen measured at 23 degrees Celsius
and 0 percent relative humidity, optionally for a structure having a thickness of
from about 72 micrometers to about 320 micrometers
[0323] In any of these aspects, the multi-layered film further comprises one or more protective
layers, each of the one or more protective layers individually comprising or consisting
essentially of a protective material, wherein each of the one or more protective layers
is adjacent to a core region and has a protective layer thickness, wherein a combination
of the one or more protective layers and the adjacent core region has a minimum radius
of curvature which is greater than a minimum radius of curvature which causes cracking
of the core region, or of one or more individual layers within the core region.
[0324] Turning to
FIG. 6, in one aspect, disclosed herein are multi-layered films, the multi-layered films
comprising one or more core regions 2160, wherein each of the one or more core regions
comprises a plurality of layers, the plurality of layers comprising gas-barrier layers
3020 comprising at least one gas-barrier material alternating with elastomeric layers
3010 comprising at least one elastomeric material; wherein each of the gas-barrier
layers has a thickness 3021 in a range of from about 0.01 micrometers to about 0.75
micrometers thick, particularly in a range of from about 0.01 micrometers to about
0.5 micrometers thick; and wherein each of the elastomeric layers has a thickness
3011 of from about 2 micrometers to about 8 micrometers thick, or from about 2 micrometers
to about 4 micrometers thick. In some aspects core region 2160 is adjacent to another
layer 3030 such as, for example, a tie layer, a structural layer, or a cap layer.
[0325] In another aspect, each of the one or more core regions comprises at least 50 layers,
or from about 50 to about 100 layers, from about 50 to about 90 layers, from about
50 to about 80 layers, from about 50 to about 70 layers, from about 60 to about 100
layers, from about 60 to about 90 layers, or from about 60 to about 80 layers. Each
of the one or more core regions has an average total thickness less than 200 micrometers,
optionally from about 125 micrometers to about 200 micrometers, or from about 125
micrometers to about 175 micrometers, or from about 150 micrometers to about 200 micrometers.
[0326] Referring now to
FIG. 7A, in an alternative aspect, a sheet or multi-layered film can incorporate single structural
layer 2200a comprising a structural material and core region 2160 comprising gas-barrier
layers.
[0327] In some aspects, the articles disclosed herein can comprise multiple layers as illustrated,
for example, in
FIG. 7B. In this exemplary embodiment, the article is a sheet comprising gas-barrier layers
and includes a two cap layers, 2120a having a thickness 2100a and 2120b having a thickness
2100b, two structural layers, 2200a having a thickness 2180a and 2200b having a thickness
2180b, and a core region 2160 having a thickness 2140. Suitable examples of thicknesses
2180a and 2180b range from about 900 micrometers to about 1990 micrometers, or from
about 900 micrometers to about 1400 micrometers, or from about 1400 micrometers to
about 1990 micrometers. Suitable examples of thickness 2140 range from about 125 micrometers
to about 200 micrometers, or from about 125 micrometers to about 175 micrometers,
or from about 150 micrometers to about 200 micrometers. Suitable examples of thicknesses
2100a and 2100b range from about 5 micrometers to about 25 micrometers. In one aspect,
the article can be two-sided. Further in this aspect, a two-sided article can include
a symmetrical arrangement of layers on both sides of core region 2160.
[0328] In one such aspect in accordance with the example of
FIG. 7B, cap layers 2120a and 2120b can comprise or consist essentially of a cap layer material.
In such an aspect, structural layers 2200a and 2200b can also comprise or consist
essentially of a structural layer material, or can comprise or consist essentially
of a barrier material. In such an aspect, the core region 2160 can comprise or consist
essentially of a multi-layered film as disclosed herein.
[0329] In any of these aspects, the cap layer 2120a can have a first surface 2120a' and
a second surface 2120a", while the cap layer 2120b can have a first surface 2120b'
and a second surface 2120b". In another aspect, the structural layer 2200a can have
a first surface 2200a' and a second surface 2200a", while the core region 2200b can
have a first surface 2200b' and a second surface 2200b". In still another aspect,
the core region 2160 can have a first surface 2160a and a second surface 2160b. In
some aspects, the second surface 2120a" of the cap layer 2120a and the first surface
2200a' of the structural layer 2200a can be adjacent to one another or otherwise in
contact with one another. In a further aspect, the second surface 2200a" of the structural
layer 2200a and the first surface 2160a of the core region and the second surface
2200a" of the structural layer 2200a can be adjacent to one another or otherwise in
contact with one another. In one aspect, the second surface 2160b of the core region
2160 and the second surface 2200b" of the structural layer 2200b can be adjacent to
one another or otherwise in contact with one another. In still another aspect, the
first surface 2200b' of the structural layer 2200b and the second surface 2120b" of
the cap layer 2120b can be adjacent to one another or otherwise in contact with one
another. In some aspects, first surface 2120a' of cap layer 2120a and/or first surface
2120b' of cap layer 2120b can independently optionally be an outer surface of an article
incorporating the multi-layered film disclosed herein. In any of these aspects, structural
layer 2200a and structural layer 2200b can be made from the same material or from
different materials and can have the same or different thicknesses. In another aspect,
cap layer 2120a and cap layer 2120b can be made from the same material or from different
materials and can have the same or different thicknesses.
[0330] In another aspect, the article can be configured as a series of four or more layers
including one or more structural layers, each of the one or more structural layers
comprising a structural layer material and including a structural layer first surface,
a structural layer second surface opposing the structural layer first surface, and
a structural layer thickness extending from the structural layer first surface to
the structural layer second surface;
optionally wherein at least one of the one or more structural layers is positioned
between the first cap layer and the core region, or between the second cap layer and
the core region; or
optionally wherein the one or more structural layers comprise two or more structural
layers, and at least a first one of the two or more structural layers is positioned
between an inner surface of a first cap layer and the first surface of a core region,
and at least a second one of the two or more structural layers is positioned between
a second surface of a core region and the inner surface of the second cap layer.
[0331] In another aspect, a first surface of a first one of the structural layers is in
contact with the inner surface of the first cap layer, and the second surface of the
first one of the structural layers is in contact with a first surface of one of the
one or more core regions, or the first surface of a second one of the one or more
structural layers is in contact with the second surface of one of the one or more
core regions, and the second surface of the second one of the structural layers is
in contact with an inner surface of the second cap layer, or both.
[0332] In one aspect, the one or more structural layers comprise or consist essentially
of the blended material or the recycled material as disclosed herein.
[0333] Referring now to
FIG. 7C, in an alternative aspect, a sheet or multi-layered film can incorporate single structural
layer 2200a comprising a structural material, single cap layer 2120a comprising a
cap layer material, and core region 2160 comprising gas-barrier layers.
[0334] In some aspects, the articles disclosed herein can comprise multiple layers as illustrated,
for example, in
FIG. 7D. In this exemplary embodiment, the article is a sheet comprising gas-barrier layers
and includes two cap layers, specifically cap layer 2120a (having a thickness 2100a),
cap layer 2120b (having a thickness 2100b); two structural layers, specifically structural
layer (2200a having a thickness 2180a), structural layer 2200b (having a thickness
2180b); two tie layers, specifically tie layer 2240a (having a thickness 2220a) and
tie layer 2240b (having a thickness 2220b); and a core region or layer 2160 (having
a thickness 2140). Suitable examples of thicknesses 2180a and 2180b range from about
900 micrometers to about 1990 micrometers, or from about 900 micrometers to about
1400 micrometers, or from about 1400 micrometers to about 1990 micrometers. Suitable
examples of thickness 2140 range from about 125 micrometers to about 200 micrometers,
or from about 125 micrometers to about 175 micrometers, or from about 150 micrometers
to about 200 micrometers. Suitable examples of thicknesses 2100a and 2100b range from
about 5 micrometers to about 25 micrometers. Suitable examples of thicknesses 2220a
and 2220b range from about 5 micrometers to about 20 micrometers. In one aspect, the
article can be two-sided. Further in this aspect, a two-sided article can include
a symmetrical arrangement of layers on both sides of core region 2160.
[0335] In one such aspect in accordance with the example of
FIG. 7D, cap layers 2120a and 2120b can comprise or consist essentially of a cap layer material.
In such an aspect, structural layers 2200a and 2200b can also comprise or consist
essentially of a structural layer material, or can comprise or consist essentially
of a barrier material. In such an aspect, the tie layers 2240a and 2240b can comprise
or consist essentially of a tie material, or can comprise or consist essentially of
a barrier material. In such an aspect, the core region 2160 can comprise or consist
essentially of a multi-layered film as disclosed herein.
[0336] In any of these aspects, the cap layer 2120a can have a first surface 2120a' and
a second surface 2120a", while the cap layer 2120b can have a first surface 2120b'
and a second surface 2120b". In another aspect, the structural layer 2200a can have
a first surface 2200a' and a second surface 2200a", while the core region 2200b can
have a first surface 2200b' and a second surface 2200b". In still another aspect,
the tie layer 2240a can have a first surface 2240a' and a second surface 2240a", while
the tie layer 2240b can have a first surface 2240b' and a second surface 2240b". In
still another aspect, the core region 2160 can have a first surface 2160a and a second
surface 2160b. In some aspects, the second surface 2120a" of the cap layer 2120a and
the first surface 2200a' of the structural layer 2200a can be adjacent to one another
or otherwise in contact with one another. In a further aspect, the second surface
2200a" of the structural layer 2200a and the first surface 2240a' of the tie layer
2240a can be adjacent to one another or otherwise in contact with one another. In
a still further aspect, the first surface 2160a of the core region and the second
surface 2240a" of the tie layer 2240a can be adjacent to one another or otherwise
in contact with one another. In one aspect, the second surface 2160b of the core region
2160 and the second surface 2240b" of the tie layer 2240b can be adjacent to one another
or otherwise in contact with one another. In another aspect, the first surface 2240b'
of the tie layer 2240b and the second surface 2200b" of the structural layer 2200b
can be adjacent to one another or otherwise in contact with one another. In still
another aspect, the first surface 2200b' of the structural layer 2200b and the second
surface 2120b" of the cap layer 2120b can be adjacent to one another or otherwise
in contact with one another. In some aspects, first surface 2120a' of cap layer 2120a
and/or first surface 2120b' of cap layer 2120b can independently optionally be an
outer surface of an article incorporating the multi-layered film disclosed herein.
In any of these aspects, structural layer 2200a and structural layer 2200b can be
made from the same material or from different materials and can have the same or different
thicknesses. In a further aspect, cap layer 2120a and cap layer 2120b can be made
from the same material or from different materials and can have the same or different
thicknesses. In a still further aspect, tie layer 2240a and tie layer 2240b can be
made from the same material or from different materials and can have the same or different
thicknesses.
[0337] Referring now to
FIG. 7E, in an alternative aspect, a sheet or multi-layered film can incorporate single structural
layer 2200a comprising a structural material, single cap layer 2120a comprising a
cap layer material, single tie layer 2240a comprising a tie layer material, and core
region 2160 comprising gas-barrier layers.
[0338] In an aspect, the article can be configured as a series of five or more layers including
one or more tie layers, each of the one or more tie layers including a tie layer first
surface, a tie layer second surface opposing the tie layer first surface, and a tie
layer thickness extending from the tie layer first surface to the tie layer second
surface;
optionally wherein at least one of the one or more tie layers is positioned between
one of the one or more structural layers and one of the one or more core regions,
or between the first cap layer and one of the one or more structural layers, or between
the second cap layer and one of the one or more structural layers, or any combination
thereof; or
optionally wherein the one or more tie layers comprise two or more tie layers, and
at least a first one of the two or more tie layers is positioned between a second
surface of a first structural layer and a first layer of a core region, and at least
a second one of the two or more tie layers is positioned between a second surface
of a core region and a first surface of a structural layer.
[0339] In one aspect, a first surface of a first one of the one or more tie layers is in
contact with a second surface of a first one of the one or more structural layers,
and the second surface of the first one of the one or more tie layers is in contact
with a first surface of a core region, or wherein a first surface of a second one
of the one or more tie layers is in contact with a second surface of one of the one
or more core regions, and the second surface of the second one of the one or more
tie layers is in contact with a first surface of a second one of the one or more structural
layers, or both.
[0340] In an aspect, the article comprises the first cap layer, a first structural layer,
a first tie layer, a core region, a second tie layer, a second structural layer, and
the second cap layer, wherein the first cap layer inner surface contacts the first
surface of the first structural layer, the second surface of the first structural
layer contacts the first surface of the first tie layer, the second surface of the
first tie layer contacts the first surface of the core region, the second surface
of the core region contacts the first surface of the second tie layer, the second
surface of the second tie layer contacts the first surface of the second structural
layer, and the second surface of the second structural layer contacts the inner layer
of the second cap layer, and optionally the core region comprises one or more core
regions, or comprises a plurality of microlayers.
[0341] One or both of the sheets comprising gas-barrier layers as shown in
FIGs. 5 and
7A-7E can independently be transparent, translucent, and/or opaque. As used herein, the
term "transparent" for a barrier layer and/or a bladder means that light passes through
the barrier layer in substantially straight lines and a viewer can see through the
barrier layer. In comparison, for an opaque barrier layer, light does not pass through
the barrier layer and one cannot see clearly through the barrier layer at all. A translucent
barrier layer falls between a transparent barrier layer and an opaque barrier layer,
in that light passes through a translucent layer but some of the light is scattered
so that a viewer cannot see clearly through the layer.
[0342] The airsole 1036 can be produced from the sheets comprising gas-barrier layers as
shown in
FIGs. 5 and
7A-7E using any suitable technique, such as thermoforming (e.g. vacuum thermoforming),
blow molding, extrusion, injection molding, vacuum molding, rotary molding, transfer
molding, pressure forming, heat sealing, casting, low-pressure casting, spin casting,
reaction injection molding, radio frequency (RF) welding, and the like. In an aspect,
the sheets comprising gas-barrier layers as shown in
FIGs. 5 and
7A-7E can be produced by co-extrusion followed by vacuum thermoforming to form the profile
of the airsole 1036 which can optionally include one or more valves (e.g., one way
valves) that allows the airsole 1036 to be filled with the fluid (e.g., gas).
[0343] In any of these aspects, the multi-layered films and articles produced therefrom
are suitable for use in mass-market articles of footwear.
[0344] In an aspect, the multi-layered films and articles formed therefrom can include one
or more textiles or one or more spacer materials, wherein the spacer materials can
be textiles, foamed components, 3D printed components, or other materials as described
herein.
[0345] Additional processes can be performed on the multi-layered films and/or articles
formed therefrom, including, but not limited to, application of decorative elements
and thermoforming to impart useful structures, shapes, or textures.
[0346] In one exemplary embodiment, provided herein is a method for producing the multi-layered
films disclosed herein, the method comprising co-extruding the gas-barrier material
and the elastomeric material to form a multi-layered structure comprising the one
or more core regions.
[0347] In one aspect, the method further comprises applying at least one tie layer to the
multi-layered film to form a multi-layered film comprising one or more core regions
and the tie layer, wherein the tie layer comprises a tie material as described herein.
In some aspects, the method comprises co-extruding at least one tie layer with the
multi-layered film to form a multi-layered film comprising the one or more core regions
and the tie layer.
[0348] In another aspect, the method comprises applying at least one structural layer to
the multi-layered film comprising the core region and the tie layer to form a multi-layered
film comprising the one or more core regions, the tie layer, and the structural layer,
wherein the structural layer comprises a structural layer material. Further in this
aspect, the method can comprise co-extruding at least one structural layer with the
multi-layered film comprising the core region and the tie layer to form a multi-layered
film comprising the one or more core regions, the tie layer, and the structural layer.
[0349] In yet another aspect, the method further comprises applying at least one cap layer
to the multi-layered film comprising the core region, the tie layer, and the structural
layer to form a multi-layered film comprising the core region, the tie layer, the
structural layer, and the cap layer, wherein the cap layer comprises a cap layer material
as described herein. In some aspects, the method further comprises co-extruding at
least one cap layer with the multi-layered film comprising the core region, the tie
layer, and the structural layer to form a multi-layered film comprising the core region,
the tie layer, the structural layer, and the cap layer.
[0350] In some aspects, the article is a layered sheet, optionally a coextruded layered
sheet or a laminated layered sheet.
[0351] In another aspect, each of the one or more core regions comprises at least 50 layers,
or from about 50 to about 100 layers, from about 50 to about 90 layers, from about
50 to about 80 layers, from about 50 to about 70 layers, from about 60 to about 100
layers, from about 60 to about 90 layers, or from about 60 to about 80 layers.
[0352] In another aspect, the gas-barrier material comprises or consists essentially of
one or more gas-barrier polymers, wherein the gas-barrier material comprises a gas-barrier
polymeric component consisting of all polymers present in the gas-barrier material.
In some aspects, the gas-barrier material comprises a nitrogen barrier material.
[0353] In an aspect, the one or more gas-barrier polymers comprise or consist essentially
of one or more thermoplastic vinylidene chloride polymers, one or more thermoplastic
acrylonitrile polymers or copolymers, one or more thermoplastic polyamides, one or
more thermoplastic epoxy resins, one or more thermoplastic amine polymers or copolymers,
or one or more thermoplastic polyolefin homopolymers or copolymers. In some aspects,
the one or more thermoplastic polyolefin homopolymers or copolymers comprise or consist
essentially of one or more thermoplastic ethylene-vinyl alcohol copolymers. In another
aspect, the one or more thermoplastic ethylene-vinyl alcohol copolymers include from
about 28 mole percent to about 44 mole percent ethylene content, or from about 32
mole percent to about 44 mole percent ethylene content.
[0354] In another aspect, the elastomeric material comprises or consists essentially of
one or more thermoplastic elastomeric polymers, and comprises an elastomeric polymeric
component consisting of all polymers present in the elastomeric material. In one aspect,
the one or more thermoplastic elastomeric polymers comprise or consist essentially
of one or more thermoplastic elastomeric polyolefin homopolymers or copolymers, one
or more thermoplastic elastomeric polyamide homopolymers or copolymers, one or more
thermoplastic elastomeric polyester homopolymers or copolymers, one or more thermoplastic
elastomeric polyurethane homopolymers or copolymers, one or more thermoplastic elastomeric
styrenic homopolymers or copolymers, or any combination thereof.
[0355] In further aspects, the one or more styrenic homopolymers or copolymers can include
one or more styrenic block copolymers, such as acrylonitrile butadiene styrene block
copolymers, styrene acrylonitrile block copolymers, styrene ethylene butylene styrene
block copolymers, styrene ethylene butadiene styrene block copolymers, styrene ethylene
propylene styrene block copolymers, styrene butadiene styrene block copolymers, and
combinations thereof.
[0356] In some aspects, the elastomeric material comprises or consists essentially of one
or more thermoplastic elastomeric polyurethane homopolymers or copolymers, and optionally
comprises or consists essentially of one or more polydiene polyol-based thermoplastic
elastomeric homopolymers or copolymers.
[0357] In one aspect, the one or more thermoplastic elastomeric polyurethane homopolymers
or copolymers comprise a plurality of first segments derived from one or more polyols
and a plurality of second segments derived from a diisocyanate. In another aspect,
the one or more thermoplastic elastomeric polyurethane homopolymers or copolymers
is a polymerization product of a diisocyanate with a polyol.
[0358] In one aspect, the thermoplastic elastomeric polyurethane homopolymer or copolymer
comprises or consists essentially of one or more polydiene polyol-based thermoplastic
elastomeric polyurethane homopolymers or copolymers and the polyol comprises or consists
essentially of a polybutadiene polyol, a polyisoprene polyol, a partially or fully-hydrogenated
derivative of a polybutadiene polyol or of a polyisoprene polyol, or any combination
thereof. In one aspect, the polyol comprises or consists essentially of a polyester
polyol, a polyether polyol, a polycarbonate polyol, a polycaprolactone polyether,
or any combination thereof.
[0359] In one aspect, the diisocyanate can comprise or consist essentially of an aliphatic
diisocyanate, an aromatic diisocyanate, or any combination thereof. In one aspect,
the aliphatic diisocyanate comprises or consists essentially of hexamethylene diisocyanate
(HDI), isophorone diisocyanate (IPDI), butylenediisocyanate (BDI), bisisocyanatocyclohexylmethane
(HMDI), 2,2,4-trimethylhexamethylene diisocyanate (TMDI), bisisocyanatomethylcyclohexane,
bisisochanatomethyltricyclodecane, norbornane diisocyanate (NDI), cyclohexane diisocyanate
(CHDI), 4,4'-dicyclohexhylmethane diisocyanate (H12MDI), diisocyanatododecane, lysine
diisocyanate, or any combination thereof. In another aspect, the aromatic diisocyanate
comprises or consists essentially of toluene diisocyanate (TDI), TDI adducts with
trimethylolpropane (TMP), methylene diphenyl diisocyanate (MDI), xylene diisocyanate
(XDI), tetramethylxylylene diisocyanate (TMXDI), hydrogenated xylene diisocyanate
(HXDI), naphthalene 1,5-diisocyanate (NDI), 1,5-tetrahydronaphthalene diisocyanate,
para-phenylene diisocyanate (PPDI), 3,3'-dimethyldiphenyl-4,4'-diisocyanate (DDDI),
4,4'-dibenzyl diisocyanate (DBDI), 4-chloro-1,3-phenylene diisocyanate, or any combination
thereof.
[0360] In one aspect, the multi-layered films disclosed herein and/or airbags or bladders
incorporating the multi-layered films can include a spacer component in an internal
cavity. For example, as shown in
FIG. 8, the spacer material can comprise or consist essentially of a textile, a foamed component,
an injection-molded component, a component produced by 3D printing or additive manufacturing,
or any combination thereof. In another aspect, the foamed component can comprise or
consist essentially of a plurality of foam particles. In one aspect, the spacer component
additionally comprises a surrounding thermoplastic material as described herein.
[0361] In one aspect, the spacer component or textile can have a decorative function, e.g.,
adding color or a pattern to a multi-layered film that is visible when an article
incorporating the multi-layered film is worn. In another aspect, the spacer component
or textile can assist in keeping layers or sheets forming a structure such as a bladder
in proper alignment with one another and can resist forces that would otherwise shift
different components of the bladder, thus stabilizing bladders, airbags, and other
articles incorporating the multi-layered films disclosed herein. In another aspect,
the internal cavity of the bladder can be hollow.
[0362] In an aspect, the spacer component can comprise a first layer, a second layer, and
a plurality of connecting members extending between and joining the first layer and
the second layer.
[0363] In some aspects, the bladder further comprises a textile. In one aspect, the textile
forms a layer of the first sheet, a layer of the second sheet, or layers of both the
first sheet and the second sheet. In one aspect, the textile forms an outer layer
of the first sheet and/or an outer layer of the second sheet, or wherein the textile
forms an inner layer of the first sheet and/or an inner layer of the second sheet.
[0364] In another aspect, the textile can be a spacer textile, the spacer textile having
a first textile face, a second textile face, and a textile thickness extending from
the first textile face to the second textile face, wherein the textile thickness is
from about 0.3 centimeters to about 3 centimeters, or from about 0.5 centimeters to
about 1 centimeter, optionally wherein a fiber density of the first textile face and
the second textile face is at least 25 percent greater, or at least 50 percent greater,
or at least 75 percent greater than a fiber density between the first textile face
and the second textile face.
[0365] In an aspect, fibers or yarns of the textile comprise or consist essentially of synthetic
fibers or yarns formed from one or more thermoplastic materials, optionally wherein
the thermoplastic materials of the synthetic fibers or yarns comprise or consist essentially
of a thermoplastic elastomeric material. In another aspect, a melting temperature
of the thermoplastic material of the synthetic fibers or yarns is within 20 degrees
Celsius of a melting temperature of a thermoplastic material forming an outer layer
of the bladder.
[0366] In one aspect, the first sheet, the second sheet, or both, comprise a layered sheet,
and a polymeric component of the thermoplastic material of the synthetic fibers or
yarns is substantially the same as a polymeric component of a thermoplastic material
of one or more layers of the first sheet and/or one or more layers of the second sheet,
optionally wherein the polymeric component of the thermoplastic material of the synthetic
fibers or yarns is substantially the same as a polymeric component of a thermoplastic
material of a cap layer or of a structural layer of the first sheet and/or the second
sheet.
[0367] In one aspect, core 3150 includes a first wall 3130a that is normally spaced apart
from a second wall 3130b at a predetermined distance as seen in
FIG. 8. A plurality of connecting members 3140 extend between first wall 3130a and second
wall 3130b. When a fluid pressurizes bladder 3100, the fluid places an outward force
on airsole layers 3110a and 31 10b. The outward force extends connecting members 3140,
thereby placing connecting members 3140 in tension and restraining further outward
movement of airsole layers 3110a and 3110b.
[0368] In a further aspect, connecting members 3140 can comprise drop yams that each include
multiple tensile filaments that are anchored to first wall 3130a and second wall 3130b.
One method of manufacturing core 3150 is double needle bar Raschel knitting. In some
aspects, a portion of first wall 3130a and second wall 3130b may be formed of air-bulked
or otherwise texturized yam, such as false twist texturized yam having a combination
of Nylon 6,6 and Nylon 6. Connecting members 3140 can be formed of a similar material.
In some aspects, first wall 3130a and second wall 3130b also include fusing filaments.
Although the thickness of core 3150, which is measured when connecting members 3140
are in a tensile state between first wall 3130a and second wall 3130b, may vary significantly
within the scope of the present disclosure, a thickness that is suitable for footwear
applications may range from 8 to 15 millimeters. In some aspects, peripheral bond
3120 can be formed by compressing and heat sealing airsole layers 3110a and 3110b
together around substantially the entire periphery of core 3150.
[0369] In some aspects, double-walled fabric cores are typically secured within an outer
barrier of a bladder by attaching a layer of thermally activated fusing agent to the
first wall and second wall of the core, and then heating the outer barrier, core,
and fusing agent to cause the fusing agent to fuse the walls of the core to the outer
barrier. The thermally activated fusing agent is typically a sheet of thermoplastic
material that is heated and pressed into contact with the first wall and the second
wall prior to placing the core between layers of the outer barrier. Although this
process could be utilized to effectively secure core 3150 and airsole layers 3110a
and 23110b to each other, this process adds a manufacturing step and additional expense
to the manufacturing process.
[0370] In an alternative aspect, a plurality of fusing filaments 3160 can be used, where
the fusing filaments 3160 that are integrated into first wall 3130a and second wall
3130b, through weaving for example. Fusing filaments 3160 are formed of a material
that will fuse, bond, or otherwise become secured to airsole layers 3110a and 3110b
when the various components of bladder 3100 are heated and compressed together.
[0371] Fusing filaments 3160 may be woven or otherwise mechanically manipulated into walls
3130a and 3130b during the double needle bar Raschel knitting process or following
the knitting process. Accordingly, fusing filaments 3160 can be integrated into walls
3130a and 3130b during the manufacturing process of core 3150, or fusing filaments
3160 can be subsequently added to walls 3130a and 3130b. The configuration of fusing
filaments 3160 and the manner in which fusing filaments 3160 are integrated into walls
3130a and 3130b may vary greatly within the scope of the present disclosure.
[0372] In some aspects, in a disclosed spacer element having a plurality of connecting members,
the spacer element comprises a textile and the plurality of members comprise yarns
or fibers which, in some aspects, comprise a spacer thermoplastic material. Further
in these aspects, the spacer element comprises a surrounding thermoplastic material
surrounding the plurality of yarns or fibers of the textile and consolidating at least
a portion of the textile, wherein the surrounding thermoplastic material has a melting
temperature lower than a melting temperature of the fiber thermoplastic material.
[0373] In other instances, in a disclosed spacer textile having a plurality of connecting
yarns or fibers, the plurality of connecting yarns or fibers comprise a spacer thermoplastic
material and a surrounding thermoplastic material surrounding the plurality of connecting
yarns or fibers of the textile and consolidating at least a portion of the textile,
wherein the surrounding thermoplastic material has a melting temperature lower than
a melting temperature of the spacer thermoplastic material.
[0374] In any of these aspects, the disclosed bladder can be a thermoformed bladder.
METHODS FOR MAKING BLADDERS AND AIRBAGS
[0375] A bladder that comprises a first sheet and a second sheet, wherein a first side of
the first sheet faces a second side of the second sheet, may be made by a method comprising:
bonding the first sheet and the second sheet together to form an internal cavity in
a space between the first side of the first sheet and the second side of the second
sheet, wherein the bond extends around at least a portion of a perimeter of the internal
cavity, optionally wherein the bond is contiguous around only one or more portions
of the perimeter of the internal cavity, and includes one or more apertures capable
of admitting a fluid to the internal cavity, forming an open cavity; or wherein the
bond is contiguous around an entire perimeter of the internal cavity, forming a sealed
bladder capable of retaining a fluid in the internal cavity;
wherein the first sheet, the second sheet, or both comprise a multi-layered film as
disclosed herein.
[0376] In another aspect, in the disclosed method, the bladder comprises one or more internal
cavities, optionally wherein the one or more internal cavities includes at least two
internal cavities, and optionally wherein each of the one or more internal cavities
is an open cavity, or each of the one or more internal cavities is a sealed bladder,
or the one or more internal cavities include at least one open cavity and at least
one sealed bladder. In still another aspect, bonding comprises adhesively bonding
or thermally bonding, optionally wherein the first sheet and the second sheet include
a thermal bond formed by radio frequency (RF) welding.
[0377] In still another aspect, the disclosed method further comprises closing the one or
more apertures in the perimeter of the internal cavity, thereby forming a sealed bladder.
In still another aspect, closing comprises forming an adhesive bond or a thermal bond
between the first side of the first sheet and the second side of the second sheet
at the one or more apertures.
[0378] In any of these aspects, the method further comprises inflating the sealed bladder
with a fluid.
METHODS FOR PRODUCING THE MULTI-LAYERED FILMS
[0379] In an aspect, the sheets comprising gas-barrier layers can be produced by co-extrusion
followed by vacuum thermoforming to form the profile of the airsole which can optionally
include one or more valves (e.g., one way valves) that allows the airsole to be filled
with the fluid (e.g., gas).
[0380] In any of these aspects, the multi-layered films and articles produced therefrom
are suitable for use in mass-market articles of footwear.
[0381] In an aspect, the multi-layered films and articles formed therefrom can include one
or more textiles or, in the case of bladders or airbags, one or more spacer materials,
wherein the spacer materials can be textiles, foamed components, 3D printed components,
or other materials as described herein.
[0382] Additional processes can be performed on the multi-layered films and/or articles
formed therefrom, including, but not limited to, application of decorative elements
and thermoforming to impart useful structures, shapes, or textures.
[0383] The multi-layered films disclosed herein may be made by a method including at least
the steps of co-extruding the gas-barrier material and the elastomeric material to
form a multi-layered film comprising one or more core regions, wherein each of the
one or more core regions comprises a plurality of layers, the plurality of layers
comprising gas-barrier layers comprising the gas-barrier material alternating with
elastomeric layers comprising the elastomeric material.
[0384] In one aspect, the disclosed method further comprises applying at least one tie layer
to the multi-layered film comprising the one or more core regions to form a multi-layered
film comprising the one or more core regions and the tie layer, wherein the tie layer
comprises a tie material as disclosed herein. In a further aspect, the disclosed method
further comprises co-extruding at least one tie layer with the multi-layered film
comprising the core region to form a multi-layered film comprising the one or more
core regions and the tie layer.
[0385] In one aspect, the disclosed method further comprises applying at least one structural
layer to the multi-layered film comprising the core region and the tie layer to form
a multi-layered film comprising the one or more core regions, the tie layer, and the
structural layer, wherein the structural layer comprises a structural layer material
as disclosed herein. In an alternative aspect, the disclosed method further comprises
co-extruding at least one structural layer with the multi-layered film comprising
the core region and the tie layer to form a multi-layered film comprising the one
or more core regions, the tie layer, and the structural layer.
[0386] In one aspect, the disclosed method further comprises applying at least one cap layer
to the multi-layered film comprising the core region, the tie layer, and the structural
layer to form a multi-layered film comprising the core region, the tie layer, the
structural layer, and the cap layer, wherein the cap layer comprises a cap layer material
as disclosed herein. In an alternative aspect, the disclosed method further comprises
co-extruding at least one cap layer with the multi-layered film comprising the core
region, the tie layer, and the structural layer to form a multi-layered film comprising
the core region, the tie layer, the structural layer, and the cap layer.
ARTICLES
[0387] Articles disclosed herein may comprise:
a first cap layer comprising or consisting essentially of a first cap layer material,
the first cap layer including a first cap layer outer surface defining a first outer
surface of the multi-layered film, a first cap inner layer surface opposing the first
cap layer outer surface, a first cap layer thickness extending from the first cap
layer inner surface to the first cap layer outer surface, wherein the first cap layer
outer surface defines a first exterior surface of the article;
a second cap layer comprising or consisting essentially of a second cap layer material,
the second cap layer including a second cap layer outer surface defining a second
outer surface of the multi-layered film, a second cap layer inner surface opposing
the second cap layer outer surface, a second cap layer thickness extending from the
second cap layer inner surface to the second cap layer outer surface, optionally wherein
the second cap layer outer surface defines a second exterior surface of the article;
and
one or more core regions as disclosed herein.
[0388] In another aspect, the first cap layer material and the second cap layer material
are substantially the same. In an alternative aspect, the first cap layer material
and the second cap layer material are different. In some aspects, the first cap layer
inner surface is in contact with the core region first surface, or the second cap
layer inner surface is in contact with the core region second surface, or both.
[0389] In another aspect, the article can be configured as a series of four or more layers
including one or more structural layers, each of the one or more structural layers
comprising a structural layer material and including a structural layer first surface,
a structural layer second surface opposing the structural layer first surface, and
a structural layer thickness extending from the structural layer first surface to
the structural layer second surface;
optionally wherein at least one of the one or more structural layers is positioned
between the first cap layer and the core region, or between the second cap layer and
the core region; or
optionally wherein the one or more structural layers comprise two or more structural
layers, and at least a first one of the two or more structural layers is positioned
between an inner surface of a first cap layer and the first surface of a core region,
and at least a second one of the two or more structural layers is positioned between
a second surface of a core region and the inner surface of the second cap layer.
[0390] In another aspect, a first surface of a first one of the structural layers is in
contact with the inner surface of the first cap layer, and the second surface of the
first one of the structural layers is in contact with a first surface of one of the
one or more core regions, or the first surface of a second one of the one or more
structural layers is in contact with the second surface of one of the one or more
core regions, and the second surface of the second one of the structural layers is
in contact with an inner surface of the second cap layer, or both.
[0391] In one aspect, the one or more structural layers comprise or consist essentially
of the blended material or the recycled material as disclosed herein.
[0392] In an aspect, the article can be configured as a series of five or more layers including
one or more tie layers, each of the one or more tie layers including a tie layer first
surface, a tie layer second surface opposing the tie layer first surface, and a tie
layer thickness extending from the tie layer first surface to the tie layer second
surface;
optionally wherein at least one of the one or more tie layers is positioned between
one of the one or more structural layers and one of the one or more core regions,
or between the first cap layer and one of the one or more structural layers, or between
the second cap layer and one of the one or more structural layers, or any combination
thereof; or
optionally wherein the one or more tie layers comprise two or more tie layers, and
at least a first one of the two or more tie layers is positioned between a second
surface of a first structural layer and a first layer of a core region, and at least
a second one of the two or more tie layers is positioned between a second surface
of a core region and a first surface of a structural layer.
[0393] In one aspect, a first surface of a first one of the one or more tie layers is in
contact with a second surface of a first one of the one or more structural layers,
and the second surface of the first one of the one or more tie layers is in contact
with a first surface of a core region, or wherein a first surface of a second one
of the one or more tie layers is in contact with a second surface of one of the one
or more core regions, and the second surface of the second one of the one or more
tie layers is in contact with a first surface of a second one of the one or more structural
layers, or both.
[0394] In an aspect, the article comprises the first cap layer, a first structural layer,
a first tie layer, a core region, a second tie layer, a second structural layer, and
the second cap layer, wherein the first cap layer inner surface contacts the first
surface of the first structural layer, the second surface of the first structural
layer contacts the first surface of the first tie layer, the second surface of the
first tie layer contacts the first surface of the core region, the second surface
of the core region contacts the first surface of the second tie layer, the second
surface of the second tie layer contacts the first surface of the second structural
layer, and the second surface of the second structural layer contacts the inner layer
of the second cap layer, and optionally the core region comprises one or more core
regions, or comprises a plurality of microlayers.
[0395] In some aspects, the article is a layered sheet, optionally a coextruded layered
sheet or a laminated layered sheet.
[0396] In another aspect, disclosed herein are articles comprising the multi-layered films
disclosed herein.
[0397] Method for Making an Article of Footwear. The article of footwear disclosed herein may be made by a method comprising securing
the disclosed bladder to an upper for an article of footwear. In another aspect, the
method further comprises securing the bladder to an outsole and a midsole chassis,
such that the bladder is disposed between the midsole chassis and the outsole, to
produce a sole structure; and securing the midsole chassis to an upper for an article
of footwear. Also disclosed herein are articles of footwear made using the disclosed
methods.
THERMOFORMING
[0398] In any of the foregoing aspects, the bladder can be subjected to a thermoforming
step, optionally wherein thermoforming occurs before inflation of the bladder, or
wherein the thermoforming step occurs simultaneously with the inflation of the bladder,
or wherein the thermoforming step occurs after the inflation of the bladder. In one
aspect, thermoforming the bladder can impart one or more structural or other properties
to the bladder, such as three-dimensional shape or structure, rigidity, abrasion resistance,
water resistance, or the like, to one or more portions of the bladder. In some aspects,
the thermoforming process can be useful in imparting a texture to the bladder, wherein
the texture can be decorative, functional, or both decorative and functional.
[0399] In an aspect, a portion of the bladder can be selectively thermoformed, for example,
by masking portions of the bladder that are not desired to be exposed to the thermoforming
process, or by using tooling that contacts or covers only a portion of the bladder.
[0400] In one aspect, the bladder comprises an outer surface and thermoforming comprises
placing the bladder in a mold, wherein the mold comprises an inner molding surface.
Further in this aspect, the inner molding surface contacts the outer surface of the
bladder.
[0401] In some aspects, a protective sheath having an outer surface is placed between at
least a portion of the outer surface of the bladder and the inner molding surface,
and the outer surface of the protective sheath contacts the inner molding surface.
In a further aspect, the protective sheath comprises an inner surface and the inner
surface of the protective sheath contacts the outer surface of the bladder. In an
optional aspect, the inner surface of the protective sheath comprises a raised pattern.
In some aspects, the raised pattern of the inner surface of the protective sheath
is imprinted into the bladder during thermoforming. In one aspect, use of a protective
sheath may be effective in reducing the number of air bubbles that form and become
trapped in any layer of the bladder during the thermoforming process.
[0402] In some aspects, thermoforming comprises increasing a temperature of the bladder
to a softening temperature of the first sheet, the second sheet, or both, conforming
the outer surface of the bladder to the shape of the inner molding surface.
[0403] In an aspect, thermoforming further comprises applying a compressive force between
the outer surface of the bladder and the inner molding surface, or optionally between
the outer surface of the protective sheath and the inner molding surface. In some
aspects, the compressive force provides a pressure differential between the outer
surface of the bladder and the inner molding surface, or optionally between the outer
surface of the protective sheath and the inner molding surface. In one aspect, the
pressure differential can be a positive pressure differential. In another aspect,
the pressure differential can be a negative pressure differential.
[0404] In any of these aspects, following thermoforming, the bladder can be cooled. During
and after cooling, in an aspect, the bladder retains shape and/or other properties
imparted during or as a result of the disclosed thermoforming process.
DECORATION
[0405] In one aspect, disclosed herein is a multi-layered film or a bladder, wherein the
multi-layered film or bladder further comprises a decorative element.
[0406] Also disclosed herein is a method for applying a decorative element to a multi-layered
film or bladder. In one aspect, the method comprises applying the decorative element
by printing, painting, brushing, or spraying the decorative element onto the multi-layered
film or bladder. In another aspect, the method comprises dipping the multi-layered
film or bladder into the decorative element, or pressing the decorative element into
the multi-layered film or bladder. In an aspect, the decorative element is in the
form of a solid, a liquid, or a gas when applied to the multi-layered film or bladder.
In an optional aspect, the decorative element comprises a pigment or a dye or both
a pigment and a dye.
[0407] In one aspect, the decorative element comprises pigments or dyes or both and the
step of applying the decorative element onto the multi-layered film or bladder comprises
curing the decorative element on the multi-layered film or bladder, optionally wherein
the curing comprises drying the decorative element, crosslinking the decorative element,
or infusing at least a portion of the decorative element into a polymeric material
of an exterior surface of the multi-layered film or bladder, or bonding the decorative
element to the exterior surface of the multi-layered film or bladder, or any combination
thereof.
[0408] In another aspect, the method includes the step of bonding the decorative element
to the exterior surface of the multi-layered film or bladder, and the bonding includes
forming an adhesive bond by applying an adhesive to a first side of the decorative
element or to the exterior surface of the multi-layered film or bladder, or both,
and then pressing together the first side of the decorative element and the exterior
surface of the multi-layered film or bladder.
[0409] In an alternative aspect, the method includes the step of bonding the decorative
element to the exterior surface of the multi-layered film or bladder, and the bonding
includes forming a thermal bond between a thermoplastic material of a first side of
the decorative element and a thermoplastic material defining the exterior surface
of the multi-layered film or bladder, by softening or melting at least an outer portion
of one or both of the thermoplastic materials, and pressing the first side of the
decorative element and the exterior surface of the multi-layered film or bladder against
each other while one or both of the thermoplastic materials are softened or melted,
and then re-solidifying the softened or melted outer portion.
[0410] In an aspect, the decorative element is applied to an exterior surface of the multi-layered
film or bladder, and, during applying or during curing or during both the applying
and the curing, the decorative element infuses into a material defining the exterior
surface of the multi-layered film or bladder, optionally wherein the decorative element
is applied as a solution of a dye.
[0411] Also disclosed herein are multi-layered films and/or bladders comprising a decorative
element applied according to any one of the disclosed methods.
ARTICLES INCORPORATING THE MULTI-LAYERED FILMS
[0412] Sole Structures. In an aspect, disclosed herein is a sole structure for an article of footwear having
an upper, the sole structure comprising a heel region disposed in a posterior end;
a forefoot region disposed in an anterior end; a mid-foot region disposed intermediately
between the heel region and the forefoot region; and a bladder as disclosed herein.
In one aspect, the bladder is disposed in the heel region.
[0413] Also disclosed are articles of footwear comprising the disclosed bladders, and articles
of footwear comprising the disclosed sole structures.
[0414] Thus, disclosed herein is an article of footwear comprising an upper and a sole structure,
wherein the upper, the sole structure, or both the upper and the sole structure comprise
a bladder, the bladder comprising:
a first film secured to a second film to define a sealed internal cavity; and
a fluid disposed within the sealed internal cavity at a pressure of about one atmosphere
(101 kilopascals) or greater;
wherein the first film, the second film or each of the first film and the second film
is a multi-layered film including a core region comprising at least 50 gas-barrier
layers and a plurality of elastomeric layers, wherein the gas-barrier layers alternate
with the elastomeric layers, wherein each of the gas-barrier layers comprises at least
one gas-barrier material and has an average thickness in a range of from about 0.01
micrometers to about 0.75 micrometers, wherein each of the elastomeric layers comprises
at least one elastomeric material and has an average thickness in a range of from
about 2 micrometers to about 8 micrometers, and wherein the core region has a total
thickness less than 200 micrometers.
[0415] In one aspect, the sole structure comprises the bladder. In another aspect, the article
of footwear further comprises a chassis secured to the upper. In still another aspect,
the article of footwear further comprises an outsole and, optionally, the outsole
is secured to the bladder. In some aspects, in the article of footwear, the bladder
can be disposed between the chassis and the outsole.
[0416] Sporting Equipment. Disclosed herein and useful for understanding the invention, but not claimed, are
articles of sporting equipment comprising the multi-layered films. The articles of
athletic equipment include any articles where flexibility and gas-barrier properties
are useful, such as, for example, inflatable balls, rafts, watercraft, mats, balance
trainers, flotation devices, and the like.
[0417] Referring now to
FIG. 9A, the multi-layered films can be incorporated into a soccer ball (useful for understanding
the invention, but not claimed). Further, the soccer ball can have outer covering
4000, one or more intermediate layers (shown herein as 4010a, 4010b, and 4010c, although
other versions having more or fewer intermediate layers should also be considered
disclosed), and an innermost gas-barrier layer 4020 comprising the disclosed multi-layered
film, wherein gas-barrier layer 4020 allows the soccer ball to maintain an inflated
state during play by reducing rates of gas (e.g., inflation air) transmission through
the multi-layered film.
FIG. 9B shows a cross-section of the soccer ball of
FIG. 9A, wherein the positioning between an innermost intermediate layer 4010c and the multi-layered
film 4020 comprising alternating gas-barrier layers 4040 and elastomeric layers 4050.
Interior 4030 is hollow and, upon inflation of the ball, is filled with air or another
gas. Interior 4030 is surrounded by the multi-layered film 4020, which provides for
a low gas-transmission rate (e.g. less than about 0.5 to about 2 cubic centimeters
per square meter per day for nitrogen measured at 23 degrees Celsius and 0 percent
relative humidity for a film having a thickness ranging from 72 micrometers to 320
micrometers).
[0418] Transportation Equipment. Also disclosed herein (and useful for understanding the invention, but not claimed)
are articles useful in transportation comprising the multi-layered films. The article
can be a tire for a bicycle, automobile, tractor, motorized scooter, motorcycle, or
any other vehicle using inflatable tires.
[0419] An exemplary tire is shown in
FIGs. 10A and
10B. Outer surface 5000 of the tire can display a pattern of treads for improved traction
and/or other aspects of operation on a road or track. Further, the tire can comprise
rubber or another material 5010 that is, in some aspects, vulcanized to enhance strength,
flexibility, and durability of the tire. Inner layer of the tire 5020 comprises the
multi-layered film disclosed herein, which, in some aspects, provides a surface area
reducing gas transmission in order to maintain inflation of the tire during use.
[0420] The multi-layered film can cover the entire inner surface of the tire including the
sidewalls (shown). Alternatively, the multi-layered film can cover a portion of the
tire. The disclosed tires can incorporate tubes or can be tubeless tires and can further
include any other layers commonly associated with a particular use (e.g. belts, noise
reduction devices, and the like, for automobile tires) in addition to the disclosed
multi-layered films.
PROPERTY ANALYSIS AND CHARACTERIZATION PROCEDURES
[0421] Specific Gravity/Density Test Protocol. The specific gravity (S.G.) or density is measured for samples taken using the Component
Sampling Procedure as described herein, using a digital balance or a Densicom Tester
(Qualitest, Plantation, Florida, USA). Each sample is weighed and then is submerged
in a distilled water bath (at 22 degrees Celsius plus or minus 2 degrees Celsius).
To avoid errors, air bubbles on the surface of the samples are removed, e.g., by wiping
isopropyl alcohol on the sample before immersing the sample in water, or using a brush
after the sample is immersed. The weight of the sample in the distilled water is recorded.
The specific gravity is calculated using the following formula:

[0422] Melting Temperature, Glass Transition Temperature, and Enthalpy of Melting Test Protocol. The melting temperature and glass transition temperature are determined using a commercially
available Differential Scanning Calorimeter ("DSC") in accordance with ASTM D3418-97,
using a sample prepared using the Material Sampling Procedure. Briefly, a 10-15 gram
sample is placed into an aluminum DSC pan and then the lid is sealed with a crimper
press. The DSC is configured to scan from -100 degrees Celsius to 225 degrees Celsius
with a 20 degree Celsius per minute heating rate, hold at 225 degrees Celsius for
2 minutes, and then cool down to 25 degrees Celsius at a rate of -10 degrees Celsius
per minute. The DSC curve created from this scan is then analyzed using standard techniques
to determine the glass transition temperature and the melting temperature. The enthalpy
of melting is calculated by integrating the area of the melting endotherm peak and
normalizing by the sample mass.
[0423] Alternatively, glass transition temperature can be determined using Dynamic Mechanical
Analysis (DMA). In this technique, a piece of the multi-layered film about 1 millimeter
thick, about 5 millimeters to about 10 millimeters wide and about 20 millimeters long
is mounted on a film tension fixture of a DMA apparatus. The sample is heated over
a pre-determined temperature range at a fixed rate of, for example, about 1 degree
Celsius to about 5 degrees Celsius per minute. During heating, the sample is tested
at fixed frequency (e.g., about 1 Hertz) and a small oscillation amplitude (e.g. about
0.05 percent strain). The storage modulus (or complex shear) is recorded.
[0424] G' is the storage modulus, representing elastic portion of the viscoelastic material.
G" is the loss modulus, representing the viscous portion. G' measures the energy stored
and G" measures the energy lost/dissipated as heat. Tan delta is the ratio of G"/G'
and the peak region is indicative of the glass transition temperature of the sample.
[0425] Melt Flow Index Test Protocol. The melt flow index is determined according to the test method detailed in ASTM D1238-13
Standard Test Method for Melt Flow Rates of Thermoplastics by Extrusion Plastometer,
using Procedure A described therein. Briefly, the melt flow index measures the rate
of extrusion of thermoplastics through an orifice at a prescribed temperature and
load. In the test method, approximately 7 grams of the material is loaded into the
barrel of the melt flow apparatus, which has been heated to a temperature specified
for the material. A weight specified for the material is applied to a plunger and
the molten material is forced through the die. A timed extrudate is collected and
weighed. Melt flow rate values are calculated in grams/10 minutes.
[0426] Creep Relaxation Temperature Test Protocol. The creep relation temperature is determined according to the exemplary techniques
described in
U.S. Patent No. 5,866,058. The creep relaxation temperature is calculated to be the temperature at which the
stress relaxation modulus of the tested material is 10 percent relative to the stress
relaxation modulus of the tested material at the solidification temperature of the
material, where the stress relaxation modulus is measured according to ASTM E328-02.
The solidification temperature is defined as the temperature at which there is little
to no change in the stress relaxation modulus or little to no creep about 300 seconds
after a stress is applied to a test material, which can be observed by plotting the
stress relaxation modulus (in Pascals) as a function of temperature (in degrees Celsius).
[0427] KIM Test Protocol. For each KIM test, a multi-layered article as described herein is extruded and formed
into a cushioning device component having an average wall thickness of between 400
micrometers and 1000 micrometers. Upon inflating the cushioning device to (15.0 pound-force
per square inch to 25.0 pound-force per square inch) about 103 kilopascals to about
172 kilopasca s with nitrogen gas, the cushioning device is intermittently compressed
by a reciprocating piston having a 101.6 mm, 127 mm, or 152.4 mm (4.0, 5.0, or 6.0
inch) diameter platen, or by a platen having a geometry similar to a shoe last to
distribute forces evenly across an entire airsole. The stroke of each piston is calibrated
as follows. The multi-layered article is first subjected to a force-controlled test
wherein the multi-layered article is taken to a peak load of 2250 Newtons, resulting
in from about 25 percent to about 70 percent compression based on inflation pressure.
The displacement at this peak load is recorded and used to set the peak displacement
in the KIM test, using a gage block. A typical KIM test is run to a predetermined
cycle count such as 320,000 or 400,000 cycles to mimic a mileage count for an average
athlete (e.g. 175 pounds and 6 feet tall).
[0428] Load Compression Test Protocol. To perform a Load Compression Test, an airsole or other cushioning device is subjected
to compression in a suitable apparatus. In one aspect, a KIM testing apparatus as
described above can be used to perform the Load Compression Test on a footwear component
such as an airsole, where the piston simulates the force of an average wearer's foot
when the component is in use (e.g., when the airsole is deformed due to a wearer taking
a step, jumping, standing, or the like). The piston or other apparatus can be held
in position for a length of time sufficient to measure distances as shown in
FIGs. 4A-4B, including heights 1046 and 1064, lengths 1050 and 1066, as well as angles 1062 and
1074. In one aspect, these heights, distances, and angles can be measured by any technique
known in the art (e.g. a ruler, caliper, laser measurement, angle finder, protractor,
smartphone or tablet app, or the like, as appropriate for the quantity being measured).
SAMPLING PROCEDURES
[0429] Using the Test Protocols described above, various properties of the materials disclosed
herein and articles formed therefrom can be characterized using samples prepared with
the following sampling procedures.
[0430] Material Sampling Procedure. The Material Sampling Procedure can be used to obtain a neat sample of a polymeric
material or of a polymer, or, in some instances, a sample of a material used to form
a polymeric material or a polymer. The material is provided in media form, such as
flakes, granules, powders, pellets, or the like. If a source of the polymeric material
or polymer is not available in a neat form, the sample can be cut from a component
or element containing the polymeric material or polymer, such as a composite element
or a sole structure, thereby isolating a sample of the material.
[0431] Component Sampling Procedure. This procedure can be used to obtain a sample of a material from a component of an
article of footwear, an article of footwear, a component of an article of apparel,
an article of apparel, a component of an article of sporting equipment, or an article
of sporting equipment. A sample including the material in a non-wet state (e.g., at
25 degrees Celsius and 20 percent relative humidity) is cut from the article or component
using a blade. If the material is bonded to one or more additional materials, the
procedure can include separating the additional materials from the material to be
tested.
[0432] The sample is taken at a location along the article or component that provides a
substantially constant material thickness for the material as present on the article
or component (within plus or minus 10 percent of the average material thickness).
For many of the test protocols described above, a sample having a surface area of
4 square centimeters is used. The sample is cut into a size and shape (e.g., a dogbone-shaped
sample) to fit into the testing apparatus. In cases where the material is not present
on the article or component in any segment having a 4 square centimeter surface area
and/or where the material thickness is not substantially constant for a segment having
a 4 square centimeter surface area, sample sizes with smaller cross-sectional surface
areas can be taken and the area-specific measurements are adjusted accordingly.
DEFINITIONS
[0433] Unless defined otherwise, all technical and scientific terms used herein have the
same meaning as commonly understood by one of ordinary skill in the art to which this
disclosure belongs. It will be further understood that terms, such as those defined
in commonly used dictionaries, should be interpreted as having a meaning that is consistent
with their meaning in the context of the specification and relevant art and should
not be interpreted in an idealized or overly formal sense unless expressly defined
herein.
[0434] All publications, patents, and patent applications cited in this specification are
cited to disclose and describe the methods and/or materials in connection with which
the publications are cited. Any lexicographical definition in the publications, patents,
and patent applications cited that is not also expressly repeated in the instant specification
should not be treated as such and should not be read as defining any terms appearing
in the accompanying claims.
[0435] This disclosure is not limited to particular aspects, embodiments, or examples described,
and as such can, of course, vary. The terminology used herein serves the purpose of
describing particular aspects, embodiments, and examples only, and is not intended
to be limiting, since the scope of the present disclosure will be limited only by
the appended claims.
[0436] Where a range of values is provided, each intervening value, to the tenth of the
unit of the lower limit unless the context clearly dictates otherwise, between the
upper and lower limit of that range and any other stated or intervening value in that
stated range, is encompassed within the disclosure. The upper and lower limits of
these smaller ranges can independently be included in the smaller ranges and are also
encompassed within the disclosure, subject to any specifically excluded limit in the
stated range. Where the stated range includes one or both of the limits, ranges excluding
either or both of those included limits are also included in the disclosure.
[0437] As will be apparent to those of skill in the art upon reading this disclosure, each
of the individual aspects, embodiments and examples described and illustrated herein
has discrete components and features which can be readily separated from or combined
with the features of any of the other several aspects, embodiments, and examples without
departing from the scope of the present disclosure. Any recited method can be carried
out in the order of events recited or in any other order that is logically possible.
[0438] Although any methods and materials similar or equivalent to those described herein
can also be used in the practice or testing of the present disclosure, the preferred
methods and materials are now described. Functions or constructions well-known in
the art cannot be described in detail for brevity and/or clarity. Aspects of the present
disclosure will employ, unless otherwise indicated, techniques of nanotechnology,
organic chemistry, materials science and engineering and the like, which are within
the skill of the art. Such techniques are explained fully in the literature.
[0439] It should be noted that ratios, concentrations, amounts, and other numerical data
can be expressed herein in a range format. Where the stated range includes one or
both of the limits, ranges excluding either or both of those included limits are also
included in the disclosure, e.g. the phrase "x to y" includes the range from 'x' to
'y' as well as the range greater than 'x' and less than `y.' The range can also be
expressed as an upper limit, e.g. `about x, y, z, or less' and should be interpreted
to include the specific ranges of `about x,' 'about y,' and `about z' as well as the
ranges of `less than x,' less than y,' and `less than z.' Likewise, the phrase `about
x, y, z, or greater' should be interpreted to include the specific ranges of `about
x,' `about y,' and `about z' as well as the ranges of `greater than x,' greater than
y,' and `greater than z.' In addition, the phrase "about 'x' to 'y'", where 'x' and
'y' are numerical values, includes "about 'x' to about 'y'". It is to be understood
that such a range format is used for convenience and brevity, and thus, should be
interpreted in a flexible manner to include not only the numerical values explicitly
recited as the limits of the range, but also to include all the individual numerical
values or sub-ranges encompassed within that range as if each numerical value and
sub-range is explicitly recited. To illustrate, a numerical range of "about 0.1 percent
to 5 percent" should be interpreted to include not only the explicitly recited values
of about 0.1 percent to about 5 percent, but also include individual values (e.g.,
1 percent, 2 percent, 3 percent, and 4 percent) and the sub-ranges (e.g., 0.5 percent,
1.1 percent, 2.4 percent, 3.2 percent, and 4.4 percent) within the indicated range.
[0440] As used herein, the term "polymer" refers to a chemical compound formed of a plurality
of repeating structural units referred to as monomers. Polymers often are formed by
a polymerization reaction in which the plurality of structural units become covalently
bonded together. When the monomer units forming the polymer all have the same chemical
structure, the polymer is a homopolymer. When the polymer includes two or more monomer
units having different chemical structures, the polymer is a copolymer. One example
of a type of copolymer is a terpolymer, which includes three different types of monomer
units. The co-polymer can include two or more different monomers randomly distributed
in the polymer (e.g., a random co-polymer). Alternatively, one or more blocks containing
a plurality of a first type of monomer can be bonded to one or more blocks containing
a plurality of a second type of monomer, forming a block copolymer. A single monomer
unit can include one or more different chemical functional groups.
[0441] Polymers having repeating units which include two or more types of chemical functional
groups can be referred to as having two or more segments. For example, a polymer having
repeating units of the same chemical structure can be referred to as having repeating
segments. Segments are commonly described as being relatively harder or softer based
on their chemical structures, and it is common for polymers to include relatively
harder segments and relatively softer segments bonded to each other in a single monomeric
unit or in different monomeric units. When the polymer includes repeating segments,
physical interactions or chemical bonds can be present within the segments or between
the segments or both within and between the segments. Examples of segments often referred
to as "hard segments" include segments including a urethane linkage, which can be
formed from reacting an isocyanate with a polyol to form a polyurethane. Examples
of segments often referred to as "soft segments" include segments including an alkoxy
functional group, such as segments including ether or ester functional groups, and
polyester segments. Segments can be referred to based on the name of the functional
group present in the segment (e.g., a polyether segment, a polyester segment), as
well as based on the name of the chemical structure which was reacted in order to
form the segment (e.g., a polyol-derived segment, an isocyanate-derived segment).
When referring to segments of a particular functional group or of a particular chemical
structure from which the segment was derived, it is understood that the polymer can
contain up to 10 mole percent of segments of other functional groups or derived from
other chemical structures. For example, as used herein, a polyether segment is understood
to include up to 10 mole percent of non-polyether segments.
[0442] The terms "Material Sampling Procedure" and "Component Sampling Procedure" as used
herein refer to the respective sampling procedures and test methodologies described
in the Property Analysis and Characterization Procedure section. These sampling procedures
and test methodologies characterize the properties of the recited materials, films,
articles and components, and the like, and are not required to be performed as active
steps in the claims.
[0443] The term "about," as used herein, can include traditional rounding according to significant
figures of the numerical value. In some aspects, the term about is used herein to
mean a deviation of 10 percent, 5 percent, 2.5 percent, 1 percent, 0.5 percent, 0.1
percent, 0.01 percent, or less from the specified value.
[0444] The articles "a" and "an," as used herein, mean one or more when applied to any feature
in aspects of the present disclosure described in the specification and claims. The
use of "a" and "an" does not limit the meaning to a single feature unless such a limit
is specifically stated. The article "the" preceding singular or plural nouns or noun
phrases denotes a particular specified feature or particular specified features and
can have a singular or plural connotation depending upon the context in which it is
used.
[0445] As used herein, the terms "about," "approximate," "at or about," and "substantially"
mean that the amount or value in question can be the exact value or a value that provides
equivalent results or effects as recited in the claims or taught herein. That is,
it is understood that amounts, sizes, formulations, parameters, and other quantities
and characteristics are not and need not be exact, but can be approximate and/or larger
or smaller, as desired, reflecting tolerances, conversion factors, rounding off, measurement
error and the like, and other factors known to those of skill in the art such that
equivalent results or effects are obtained. In some circumstances, the value that
provides equivalent results or effects cannot be reasonably determined. In such cases,
it is generally understood, as used herein, that "about" and "at or about" mean the
nominal value indicated ± 10 percent variation unless otherwise indicated or inferred.
In general, an amount, size, formulation, parameter or other quantity or characteristic
is "about," "approximate," or "at or about" whether or not expressly stated to be
such. It is understood that where "about," "approximate," or "at or about" is used
before a quantitative value, the parameter also includes the specific quantitative
value itself, unless specifically stated otherwise.
[0446] As used herein, the phrase "consists essentially of" or "consisting essentially of"
refer to the feature being disclosed as having primarily the listed feature without
other active components (relative to the listed feature) and/or those that do not
materially affect the characteristic(s) of the listed feature. For example, the gas-barrier
material can consist essentially of a gas-barrier material, which means that gas-barrier
material can include fillers, colorants, etc. that do not substantially interact with
or interact with the change the function or chemical characteristics of the gas-barrier
material. In another example, the gas-barrier material can consist essentially of
a thermoplastic ethylene-vinyl alcohol copolymer, which means that the gas-barrier
material does not include a sufficient amount of another type of thermoplastic polymer
or copolymer to alter the properties (e.g., melting temperature, melt flow index,
creep relaxation temperature, or the like) of the gas-barrier material. Further in
this aspect, when the gas-barrier material consists essentially of one polymer type
(e.g., a thermoplastic ethylene-vinyl alcohol copolymer), it may contain less than
1 weight percent of another type of polymer.
[0447] As used herein, "polyurethane" refers to a copolymer (including oligomers) that contains
a urethane group (-N(C=O)O-). These polyurethanes can contain additional groups such
as ester, ether, urea, allophanate, biuret, carbodiimide, oxazolidinyl, isocynaurate,
uretdione, carbonate, and the like, in addition to urethane groups. In an aspect,
one or more of the polyurethanes can be produced by polymerizing one or more isocyanates
with one or more polyols to produce copolymer chains having (-N(C=O)O-) linkages.
[0448] As used herein, the terms "at least one" and "one or more of" an element are used
interchangeably, and have the same meaning that includes a single element and a plurality
of the elements, and can also be represented by the suffix "(s)" at the end of the
element. For example, "at least one polyurethane," "one or more polyurethanes," and
"polyurethane(s)" can be used interchangeably and have the same meaning.
[0449] As used herein, a "sheet" or "film" refers to a flexible strip comprising one or
more polymeric materials, the sheet or film having a thickness that is much smaller
than its length and/or width. As used herein, a "core layer" may refer to an internal
layer of material in a multi-layer sheet or film. Similarly, as used herein, a "core
region" may refer to one or more layers which is, or which together form, an internal
region of material in a multi-layer sheet or film. As used herein, a "cap layer" may
refer to an externally-facing layer of material in a multi-layer sheet or film. Also
as used herein, a "structural layer" may refer to a layer of material in a multi-layer
sheet or film that is disposed between a cap layer and a core layer. As used herein,
a "tie layer" may also refer to an internal layer in a multi-layer sheet or film;
wherein, typically, a tie layer comprises a material which increases a bond strength
of the adjacent layers.
[0450] When an element or layer is referred to as being "on," "engaged to," "connected to,"
"attached to," or "coupled to" another element or layer, it may be directly on, engaged,
connected, attached, or coupled to the other element or layer, or intervening elements
or layers may be present. In contrast, when an element is referred to as being "directly
on," "directly engaged to," "directly connected to," "directly attached to," or "directly
coupled to" another element or layer, there may be no intervening elements or layers
present. Other words used to describe the relationship between elements should be
interpreted in a like fashion (e.g., "between" versus "directly between," "adjacent"
versus "directly adjacent," etc.). As used herein, the term "and/or" includes any
and all combinations of one or more of the associated listed items.
[0451] The terms first, second, third, etc. may be used herein to describe various elements,
components, regions, layers and/or sections. These elements, components, regions,
layers and/or sections should not be limited by these terms. These terms may be only
used to distinguish one element, component, region, layer, or section from another
region, layer, or section. Terms such as "first," "second," and other numerical terms
do not imply a sequence or order unless clearly indicated by the context. Thus, a
first element, component, region, layer, or section discussed below could be termed
a second element, component, region, layer, or section without departing from the
teachings of the example configurations.
[0452] As used herein, the terms "crack," "cracking," "craze," "crazing," "break," and "breakage"
may be used interchangeably, to describe a fracture in the gas-barrier material forming
one or more gas-barrier layers in a core region of a multi-layered film. As described
below, the degree or level of cracking can be classified as being "severe cracking,"
"mild cracking" or "little to no cracking," based on the extent of the fracture within
the core region and the effects the cracking has on the properties (including gas
transmission rate and clarity) of a multi-layered film.
[0453] "Little to no cracking" may describe a level of cracking in which no cracking is
present in the gas-barrier core, or in which a single fracture in the gas-barrier
material of a gas-barrier layer of the core may extend within or across only a single
gas-barrier layer, or only a few gas-barrier layers (and the elastomer layers directly
adjacent to them). For example, the extent of an individual fracture can be determined
by viewing a magnified cross-section of the thickness of the core region of the film.
When observed in this manner, typically either no cracking in the gas-barrier layers
is observed, or fractures which affect less than 20 percent of the gas-barrier layers,
or fractures which affect less than 20 percent of the cross-sectional thickness of
the core region, are observed. Typically, the edges of any fractures which are present
do not pull away from each other and create a gap in the core region. FIG. 11C shows
micrographs of two cross-sectional thicknesses of core regions of a multi-layer film,
both of which exhibit little to no cracking. A multi-layer film exhibiting little
to no cracking typically does not have any cracking or crazing which is visible to
the naked eye, and has an acceptably low rate of gas transmission.
[0454] "Mild cracking" may describe a level of cracking in which a single fracture in the
gas-barrier may extend across a few gas-barrier layers or across several gas-barrier
layers (and the elastomer layers directly adjacent to them), but which does not extend
across a majority of the of gas-barrier layers and elastomer layers present in the
core region, or which does not extend across a majority of the total thickness of
the core region. For example, the extent of an individual fracture can be determined
by viewing a magnified cross-section of the thickness of the core region of the film.
When observed in this manner, typically fractures which effect 3-10 gas-barrier layers,
or fractures which effect less than 50 percent of the gas-barrier layers, or fractures
which effect less than 50 percent of the cross-sectional thickness of the core region,
are observed. While the edges of some fractures may pull away from each other and
create a small gap in the core region, this does not occur in the majority of the
fractures.
FIG. 11B shows micrographs of two cross-sectional thicknesses of core regions of a multi-layer
film, both of which exhibit mild cracking. A multi-layer film exhibiting mild cracking
may exhibit a small decrease in transparency, as the presence of mild cracks may make
the film appear somewhat hazy. In some examples, a few of the mild cracks may be visible
to the naked eye.
[0455] "Severe cracking" may describe a level of cracking in which a single fracture in
the gas-barrier layers of the core may extend across a majority of the gas-barrier
layers and elastomer layers present in the core region, or across a majority of the
thickness of the core region. For example, the extent of an individual fracture can
be determined by viewing a magnified cross-section of the thickness of the core region
of the multi-layer film. When observed in this manner, a fracture may extend across
at least 50 percent of a cross-sectional thickness of the core region, or across more
than 75 percent of the cross-sectional thickness of the core region, or across the
entire cross-sectional thickness of the core region. Often, the edges of fractures
pull away from each other and create a gap in the core region.
FIG. 11A shows micrographs of two cross-sectional thicknesses of core regions of a multi-layer
film, both of which exhibit severe cracking. A multi-layer film exhibiting severe
cracking typically will exhibit an unacceptably high rate of gas diffusion, has a
decreased level of transparency as compared to its initial level of transparency,
and includes cracks and crazes which are visible to the naked eye.
EXAMPLES
[0456] The present disclosure is more particularly described in the following examples that
are intended as illustrations only, since numerous modifications and variations within
the scope of the present disclosure will be apparent to those skilled in the art.
[0457] Example 1. Multi-layer Control and Test Films were prepared and formed into Control and Test
Bladders. These Bladders were subjected to repeated flexing and releasing cycles to
simulate the conditions to which bladders are exposed to during wear when used as
cushioning elements in a midsole of an article of footwear.
[0458] The Control and Test Films were all extruded films and all included a gas-barrier
core region formed by extruding a gas-barrier material and an elastomeric material
in alternating layers. The same gas-barrier material (including ethylene-vinyl alcohol)
and the same elastomeric material (including thermoplastic polyurethane) were used
in the Control and Test Films. Each Film also included a structural layer positioned
on either side of the core region (2 structural layers total), and a cap layer on
each film surface (2 cap layers total). The structural layers of the Control and Test
Films were formed of the same materials as each other (including thermoplastic polyurethane).
The cap layers of the Control and Test Films were also formed of the same materials
as each other (including thermoplastic polyurethane).
[0459] The Bladders were prepared by thermoforming two films of the same type (i.e., 2 Control
Films for the Control Bladder, 2 Test Films for a Test Bladder), bonding the two films
to each other to form the perimeter of the bladder, and filling the bladder with nitrogen
gas, to form a sealed bladder containing the nitrogen gas at a pressure of about 138
Kilopascals.
[0460] The sealed Control and Test Bladders were then each subjected to a number of KIM
test cycles. Following about 350,000 (350k) to about 400,000 (400k) KIM test cycles,
the appearance of the Films of the Bladders was assessed by the naked eye and assigned
a Cracking Level (Severe, Mild, or Little-to-No cracking). Samples of the core regions
of areas of the Films exhibiting cracking visible to the naked eye were taken and
inspected microscopically. When Little-to-No cracking was visible to the naked eye,
the regions of the Test Bladders selected for microscopy corresponded to the same
areas where extensive cracking was observed in the Control Bladders.
[0461] The Control Films each included a gas-barrier core region including 32 gas-barrier
layers and 32 elastomeric layers, with each gas-barrier layer directly adjacent to
an elastomeric layer in an alternating pattern. In the Control Film, the thickness
of the individual gas-barrier layers ranged from about 1.0 micrometers to about 1.2
micrometers. Each of the two Control Films individually had a total thickness of about
25.4-30.8 micrometers. Following about 350,000 KIM cycles, the Control Films of the
Control Bladder exhibited Severe racking.
FIG. 11A shows micrographs of cross-sections of core regions of areas of the Control Film
exhibiting cracking visible to the naked eye, taken from the Control Bladder after
about 350k KIM cycles.
[0462] The First Test Films each included a gas-barrier core region including 32 gas-barrier
layers and 32 elastomeric layers with each gas-barrier layer directly adjacent to
an elastomeric layer in an alternating pattern. In the First Test Film, the thickness
of the individual gas-barrier layers were about 75 percent as thick as the individual
gas-barrier layers in the Control Film, and so ranged from about 0.8 micrometers to
about 0.9 micrometers. Following about 400k KIM cycles, the First Test Films of the
First Test Bladder exhibited Mild cracking based on visual inspection by the naked
eye and microscopy.
FIG. 11B shows micrographs of cross-sections of core regions of areas of the First Test Film
exhibiting mild cracking visible to the naked eye, taken from the First Test Bladder
after about 400k KIM cycles.
[0463] The Second Test Films each included a gas-barrier core region including 32 gas-barrier
layers and 32 elastomeric layers in the same alternating pattern as described above.
In the Second Test Film, the thickness of the individual gas-barrier layers were about
50 percent as thick as the individual gas-barrier layers in the Control Film, and
so ranged from about 0.5 micrometers to about 0.6 micrometers. Following about 400k
KIM cycles, the Second Test Films of the Second Test Bladder exhibited Little-to-No
cracking, based on visual inspection using the naked eye as well as microscopy.
FIG. 11C shows micrographs of cross-sections of core regions of areas of the First Test Film
exhibiting mild cracking visible to the naked eye, taken from the Second Test Bladder
after about 400k KIM cycles.
[0464] Example 2. Multi-layer Control and Test Films were prepared and formed into Control and Test
Bladders as described in Example 1. These Bladders were subjected to repeated flexing
and releasing cycles to simulate the conditions to which bladders are exposed to during
wear when used as cushioning elements in a midsole of an article of footwear. The
sealed Control and Test Bladders were each subjected to a total of 400,000 (400k)
KIM test cycles. Before the KIM testing and following 60,000 (60k), 120,000 (120k),
and/or 320,000 (320k) KIM test cycles, the gas transmission rate was measured for
each of the Bladders (see
FIGS. 12A, 13A, and
14 for the exact number of cycles after which the gas transmission rate of the Control
and Test Bladders were measured). Gas transmission rates (GTR) were measured in cubic
centimeters per square meter per day. The measured gas transmission rates were used
to develop a gas transmission rate fatigue model using the following equation:

where G is gas transmission rate, G
0 is the gas transmission rate prior to any KIM cycling, G
m is the gas transmission rate after 320,000 KIM cycles, and k is a growth parameter
depending on gas-barrier layer thickness as well as the type and number of gas-barrier
layers in the films of the bladder. Following 400,000 (400k) KIM test cycles, the
appearance of the Films of the Bladders was assessed as described in Example 1.
[0465] Example 2A. The Control Films and Control Bladder, as well as the Second Test Films and Second
Test Bladders used in Example 2A were the same as in Example 1. The Third Test Films
each included a gas-barrier core region including 24 gas-barrier layers alternating
with 24 elastomeric layers, 33 percent fewer gas-barrier layers than in the Control
and Second Test Films. In the Third Test Film, the thickness of individual gas-barrier
layers was about 50 percent of individual gas-barrier layers in the Control Film,
and so ranged from about 0.5 micrometers to about 0.6 micrometers.
[0466] FIG. 12A shows the GTRs measured for the Control Bladder (bottom curve) and for the Second
Test Bladder (middle curve), and for the Third Test Bladder (top curve) after the
indicated number of KIM cycles.
FIG. 12A also shows the GTR calculated using the above equation for 240,000 KIM cycles (GTR
240k). Unexpectedly, the measured and calculated GTRs for both the Second and Third Test
Bladders were all only slightly higher than for the Control Bladder and were still
comfortably below the desired maximum of 3 cubic centimeters per square meter per
day. This was unexpected as the gas-barrier layers of both the Second and Third Test
films were 50 percent thinner than those of the Control Film, and the Third Test Film
contained 33 percent fewer of these thinner gas-barrier layers than the Second and
Control Test Films.
[0467] As in Example 1, following 400k KIM cycles, areas of the Control Films of the Control
Bladder exhibited Severe cracking, while areas of the Second Test Films of the Second
Test Bladder exhibited Little-to-No cracking. The Third Test Films of the Third Test
Bladder also exhibited Little-to-No cracking.
FIG. 12B shows micrographs of cross-sections of core regions of areas of the Second Test Film.
FIG. 12C shows micrographs of cross-sections of core regions of areas of the Third Test Film
exhibiting Little-to-No cracking.
[0468] Example 2B. The Control Films and Control Bladder, as well as the First Test Films and First
Test Bladders used in Example 2B were the same as in Example 1. The Third Test Films
and the Third Test Bladder were the same as in Example 2A.
[0469] FIG. 13A shows the GTRs measured for the Control Bladder (bottom curve) and for the First
Test Bladder (middle curve), and for the Third Test Bladder (top curve) after the
indicated number of KIM cycles.
FIG. 13A also shows the GTR calculated as in Example 2A. As in Example 2A, unexpectedly, the
measured and calculated GTRs for both the First and Third Test Bladders were all only
slightly higher than for the Control Bladder and were still comfortably below the
desired maximum of 3 cubic centimeters per square meter per day. The calculated GTR
for the First Test Bladder (2.10 cc/m
2·day) was only slightly lower than the GTR calculated for the Second Test Bladder
(2.15 cc/m
2·day). This was unexpected as the gas-barrier layers of the Second Test Film were
about a third thinner than the First Test Film (the thickness of the gas-barrier layers
in the Second Test Film were about 50 percent of the thickness as the gas-barrier
layers in the Control Film, while the thickness of the gas-barrier layers in the First
Test Film were about 75 percent of the thickness of the gas-barrier layers in the
Control Film).
[0470] As in Examples 1 and 2A, following 400k KIM cycles, areas of the Control Films of
the Control Bladder exhibited Severe cracking, while areas of the First Test Films
of the First Test Bladder exhibited Mild cracking, and the Third Test Films of the
Third Test Bladder exhibited Little-to-No cracking.
FIG. 13B shows micrographs of cross-sections of core regions of areas of the First Test Film.
[0471] Example 2C. The Control Films and Control Bladder used in Example 2C were the same as in Example
1. The Fourth Test Films each included a gas-barrier core region including 40 gas-barrier
layers alternating with 40 elastomeric layers as described above. The Fourth Test
Films included 25 percent more gas-barrier layers than in the Control Films. In the
Fourth Test Films, the thickness of the individual gas-barrier layers was the same
as in the Control Films, and so ranged from about 1.0 micrometers to about 1.2 micrometers.
The Fifth Test Films each included a gas-barrier core region including 60 gas-barrier
layers alternating with 60 elastomeric layers as above. The Fifth Test Films included
over 87 percent more gas-barrier layers than in the Control Films. In the Fifth Test
Films, the thickness of the individual gas-barrier layers was 150 percent of their
thickness in the Control Films, and so ranged from about 1.5 micrometers to about
1.8 micrometers.
[0472] FIG. 14 shows the GTRs measured for the Fourth Test Bladder (top curve), and for the Fifth
Test Bladder (bottom curve) after the indicated number of KIM cycles.
FIG. 13A also shows the GTR calculated as in Examples 2A and 2B. The measured and calculated
GTRs for the Fifth Test Bladder was lower than for the Control Bladder other Test
Bladders, as would be expected based on the increased thickness and number of the
gas-barrier layers. The measured and calculated GTR (2.24 cubic centimeters per square
meter per day) for the Fourth Test Bladder were higher than for the Fifth Test Bladder,
but surprisingly were also higher than for the First and Second Test Bladders (calculated
GTR of 2.10 cubic centimeters per square meter per day and 2.15 cubic centimeters
per square meter per day, respectively). This was unexpected as the First and Second
Test Films each had thinner gas-barrier layers and fewer gas-barrier layers than the
Fourth Test Film.
[0473] As in Examples 1, 2A and 2B, following 400k KIM cycles, areas of the Control Films
of the Control Bladder exhibited Severe cracking, while areas of the Fourth Test Films
of the Fourth Test Bladder and of the Fifth Test Films of the Fifth Test Bladder both
exhibited Mild cracking.
[0474] The results of Examples 1 to 2C are summarized in Table 1.

[0475] As a person skilled in the art will readily appreciate, the above description is
meant as an illustration of the implementation of the principles of this invention.
This description is not intended to limit the scope or application of this invention
in that the invention is susceptible to modification, variation, and change, without
departing from the invention as defined in the following claims.