TECHNICAL FIELD
[0001] The present invention relates to an artificial leather which includes a fiber entanglement
including ultrafine fibers, an elastomer, and a functional agent (flame retardant
or the like), has moderate air permeability and a flexible texture, is excellent in
flame retardancy, and has feels like natural suede and an elegant appearance. The
present invention also relates to an artificial leather backing material used for
obtaining the artificial leather, and having good formability of an opening portion.
BACKGROUND ART
[0002] Conventionally, an artificial leather including a fiber entanglement formed of ultrafine
fibers and an elastomer and having raised nap has excellent characteristics in air
permeability, durability, uniformity of quality, and the like as compared with natural
leather, and is used not only as a clothing material but also in various fields such
as interior materials of public transporters such as aircrafts, ships, and railroad
vehicles, interior materials for vehicles, interior materials, building materials,
and miscellaneous goods.
[0003] In the fields described above, artificial leather is often required to have high
flame retardant performance, and in the fields where flame retardancy is required,
it is common that the artificial leather includes a flame retardant. Among them, in
order to cope with a ventilation system particularly in an interior material for vehicles,
moderate air permeability is required by the density and material configuration of
artificial leather and control of an opening portion.
[0004] Meanwhile, in order to develop the flame retardancy in the artificial leather, methods
such as applying a flame retardant to ultrafine fibers, applying the flame retardant
to the entire artificial leather, and coating and applying the flame retardant to
one surface of the artificial leather are adopted.
[0005] However, in the artificial leather obtained by these methods, the elastomer such
as polyurethane constituting the artificial leather and an ultrafine thermoplastic
synthetic fiber constituting a nonwoven fabric, a woven fabric, or a knitted fabric
are different from each other in a mechanism developing flame retardancy, and therefore,
it is known that it is very difficult to make the entire artificial leather flame
retardant.
[0006] In order to solve such a problem of flame retardancy, it has been proposed that an
organic phosphorus component copolymerized polyester is used for ultrafine fibers
of artificial leather (for example, see Patent Document 1), a polyurethane elastomer
obtained by copolymerizing an organic phosphorus component is used for an elastomer
of artificial leather (for example, see Patent Document 2), or a diaryl phosphoramidate-based
flame retardant is attached to ultrafine fibers and exhausted (for example, see Patent
Document 3).
[0007] In addition, there have been proposed a method in which a base formed of a flame-retardant
heat-resistant fiber is stacked on a back surface and integrated by entanglement (for
example, see Patent Document 4), a method in which a flame retardant is partially
applied so as to have an area ratio of 60 to 90% in order to secure a certain air
permeability when the flame retardant is applied to a back surface of artificial leather
(for example, see Patent Document 5), and a method in which vent holes penetrating
the artificial leather are formed (for example, see Patent Document 6).
PRIOR ART DOCUMENTS
PATENT DOCUMENTS
SUMMARY OF THE INVENTION
PROBLEMS TO BE SOLVED BY THE INVENTION
[0009] In the technique as disclosed in Patent Document 1, the organophosphorus component
is copolymerized as compared with polyester usually used for ultrafine fibers, so
that spinnability and dye dyeability at the time of production are deteriorated. In
addition, since thread strength of ultrafine fibers and rubbing fastness of the artificial
leather decrease, it is difficult to use the artificial leather for applications requiring
high light resistance and high abrasion resistance.
[0010] In the technique as disclosed in Patent Document 2, the organophosphorus component
is copolymerized with a polyurethane component that is an important constituent material
for imparting strength and texture to the artificial leather without aged deterioration,
and the design is such that texture and durability are lowered as compared with normal
polyurethane.
[0011] In the technique as disclosed in Patent Document 3, when the diaryl phosphoramidate-based
flame retardant is attached without using a binder, the flame retardant may fall off
during use, and the flame retardancy becomes unstable. On the other hand, when the
flame retardant is attached with a binder, a tactile sensation of a surface of the
artificial leather becomes a hard feel. In addition, as disclosed in the background
art of Patent Document 3, in a case where a water-soluble flame retardant such as
guanidine phosphate is added to the entire artificial leather, when a napped surface
is subjected to a process of absorbing moisture and then drying, there occurs a phenomenon
that the guanidine phosphate is dissolved by the moisture and transferred to the surface
to form a cyclic stain, that is, so-called "water spot", and there is a problem that
designability of the artificial leather is significantly impaired.
[0012] In the technique as disclosed in Patent Document 4, it is necessary to have a sufficient
basis weight of the flame-retardant heat-resistant fiber in order to secure a certain
flame retardancy, and denseness of an entangled structure of the artificial leather
is reduced, so that an elegant appearance and a flexible texture tend to be impaired.
A method of integrating by entanglement by inserting into the inside and intertwining
and integrating the flame-retardant heat-resistant fiber and a method of mixing flame-retardant
heat-resistant fiber with constituent fiber also have the same problem.
[0013] In the technique as disclosed in Patent Document 5, since the flame retardant is
applied in a dot shape, sufficient flame retardancy is not obtained, and a preliminary
artificial leather does not have sufficient air permeability, so that it is not possible
to achieve both denseness for an elegant appearance and air permeability that can
be compatible with, for example, a ventilation system.
[0014] In the technique as disclosed in Patent Document 6, in the punching by a punching
roll, a scrap after the punching is likely to clog a sheet or the punching roll, and
mass production is difficult.
[0015] To summarize the above, in the techniques as disclosed in Patent Documents 1 to 6,
in the artificial leather including a fiber entanglement formed of ultrafine fibers
difficult to be made flame retardant and an elastomer, the artificial leather achieving
both the flame retardancy and other important characteristics (in particular, moderate
air permeability, flexible texture, feels like natural suede, and elegant appearance)
cannot be provided.
[0016] Thus, the present invention has been made in view of the above circumstances, and
an object thereof is to provide an artificial leather having excellent functionality
(flame retardancy and the like) while having moderate air permeability and a flexible
texture, and having feels like natural suede and an elegant appearance. Another object
of the present invention is to provide an artificial leather backing material used
for obtaining the artificial leather, and having good formability of an opening portion.
SOLUTIONS TO THE PROBLEMS
[0017] As a result of intensive studies by the present inventors to achieve the above object,
it has been found that in an artificial leather including an ultrafine fiber entanglement,
an elastomer, and a functional agent (flame retardant or the like), when the form
of existence of the functional agent (flame retardant or the like) is within a specific
range and tackiness of the functional agent (flame retardant or the like) is within
a specific range, an artificial leather having good formability and achieving both
functionality (flame retardancy or the like) and other important characteristics can
be provided even if an opening portion is provided in the artificial leather.
[0018] The present invention has been completed based on these findings. The present invention
provides the following inventions.
[0019] The artificial leather of the present invention is an artificial leather including
a fiber entanglement including an ultrafine fiber having an average single fiber diameter
of 0.1 um or more and 10 um or less, and an elastomer, in which one surface is a napped
surface having a raised nap, the other surface is a flame retardant surface having
a flame retardant, and the following requirements 1 and 2 are satisfied.
Requirement 1: At least the flame retardant surface has a plurality of opening portions.
Requirement 2: The flame retardant has a tackiness of 0.1 N/cm2 or more and 2.0 N/cm2 or less.
[0020] According to a preferred aspect of the artificial leather of the present invention,
an opening ratio of the flame retardant surface is 1% or more and 40% or less.
[0021] According to a preferred aspect of the artificial leather of the present invention,
the artificial leather has a plurality of opening portions in each of the napped surface
and the flame retardant surface, and at least some of the opening portions are through
opening portions formed to penetrate from the napped surface to the flame retardant
surface.
[0022] According to a preferred aspect of the artificial leather of the present invention,
the fiber entanglement is formed by integrating a fiber entanglement including the
ultrafine fiber and a woven/knitted fabric (a).
[0023] According to a preferred aspect of the artificial leather of the present invention,
the flame retardant surface is a surface formed by stacking a woven/knitted fabric
(b).
[0024] According to a preferred aspect of the artificial leather of the present invention,
a presence ratio of the flame retardant in a thickness direction satisfies the following
formula:

where W is a thickness (mm) from the flame retardant surface where the flame retardant
is present, and W
0 is a thickness (mm) of the entire artificial leather.
[0025] According to a preferred aspect of the artificial leather of the present invention,
the flame retardant contains a phosphorus-based compound.
[0026] According to a preferred aspect of the artificial leather of the present invention,
the fiber entanglement including the elastomer has a density of 0.20 g/cm
3 or more and 0.50 g/cm
3 or less.
[0027] In a production method for an artificial leather of the present invention, a flame
retardant having a tackiness of 0.1 N/cm
2 or more and 2.0 N/cm
2 or less is applied to one surface of a napped sheet-shaped article including a fiber
entanglement including ultrafine fibers having an average single fiber diameter of
0.1 um or more and 10 um or less and an elastomer to form a flame retardant surface,
and a plurality of opening portions are provided on at least the flame retardant surface.
[0028] An artificial leather backing material of the present invention is an artificial
leather backing material including a fiber entanglement including an ultrafine fiber
having an average single fiber diameter of 0.1 um or more and 10 um or less, and an
elastomer, in which one surface is a napped surface having a raised nap, the other
surface is a functional surface having a functional agent, and the functional agent
has a tackiness of 0.1 N/cm
2 or more and 2.0 N/cm
2 or less. The artificial leather backing material can be used as the artificial leather
of the present invention by forming an opening portion, and the artificial leather
backing material itself can also be used as an artificial leather.
[0029] An artificial leather backing material of the present invention is an artificial
leather backing material including a fiber entanglement including an ultrafine fiber
having an average single fiber diameter of 0.1 um or more and 10 um or less, and an
elastomer, in which one surface is a napped surface having a raised nap, and the other
surface is a functional surface having a functional agent, the functional surface
has a Kinetic friction coefficient of 0.15 or more and 0.60 or less, and the artificial
leather backing material has a stiffness of 30 mm or more and 150 mm or less.
[0030] An artificial leather backing material of the present invention is an artificial
leather backing material including a fiber entanglement including an ultrafine fiber
having an average single fiber diameter of 0.1 um or more and 10 um or less, and an
elastomer, in which one surface is a napped surface having a raised nap, the other
surface is a functional surface having a functional agent, and an adhesion amount
of the functional agent is 2 to 30% by mass with respect to the artificial leather
backing material.
EFFECTS OF THE INVENTION
[0031] According to the present invention, it is possible to obtain an artificial leather
having excellent functionality (flame retardancy and the like) while having moderate
air permeability and a flexible texture, and having feels like natural suede and an
elegant appearance. In addition, it is possible to obtain an artificial leather backing
material used for obtaining the artificial leather, and having good formability of
an opening portion.
EMBODIMENTS OF THE INVENTION
[0032] The artificial leather of the present invention is an artificial leather including
a fiber entanglement including an ultrafine fiber having an average single fiber diameter
of 0.1 um or more and 10 um or less, and an elastomer, in which one surface is a napped
surface having a raised nap, the other surface is a flame retardant surface having
a flame retardant, and the following requirements 1 and 2 are satisfied.
Requirement 1: At least the flame retardant surface has a plurality of opening portions.
Requirement 2: The flame retardant has a tackiness of 0.1 N/cm2 or more and 2.0 N/cm2 or less.
[0033] A ratio by weight of the ultrafine fiber contained in the fiber entanglement is
preferably 60% or more, more preferably 80% or more.
[0034] An artificial leather backing material of the present invention is an artificial
leather backing material including a fiber entanglement including an ultrafine fiber
having an average single fiber diameter of 0.1 um or more and 10 um or less, and an
elastomer, in which one surface is a napped surface having a raised nap, the other
surface is a functional surface having a functional agent, and the functional agent
has a tackiness of 0.1 N/cm
2 or more and 2.0 N/cm
2 or less.
[0035] An artificial leather backing material of the present invention is an artificial
leather backing material including a fiber entanglement including an ultrafine fiber
having an average single fiber diameter of 0.1 um or more and 10 um or less, and an
elastomer, in which one surface is a napped surface having a raised nap, and the other
surface is a functional surface having a functional agent, the functional surface
has a Kinetic friction coefficient of 0.15 or more and 0.60 or less, and an artificial
leather has a stiffness of 30 mm or more and 150 mm or less.
[0036] An artificial leather backing material of the present invention is an artificial
leather backing material including a fiber entanglement including an ultrafine fiber
having an average single fiber diameter of 0.1 um or more and 10 um or less, and an
elastomer, in which one surface is a napped surface having a raised nap, the other
surface is a functional surface having a functional agent, and an adhesion amount
of the functional agent is 2 to 30% by mass with respect to the artificial leather
backing material. Hereinafter, the constituent elements will be described in detail,
but the present invention is not limited to the scope described below at all as long
as the gist thereof is not exceeded.
[Fiber entanglement]
[0037] The fiber entanglement constituting the artificial leather of the present invention
includes an ultrafine fiber, and the ultrafine fiber has an average single fiber diameter
of 0.1 um or more and 10 um or less. When the average single fiber diameter of the
ultrafine fiber is 0.1 um or more, preferably 1.5 um or more, an excellent effect
of coloring property after dyeing, light resistance, fastness to rubbing, and stability
during spinning is exhibited, and strength of the artificial leather that withstands
practical use can be obtained. On the other hand, when the average single fiber diameter
is 10.0 µm or less, preferably 6.0 µm or less, more preferably 4.5 µm or less, it
is possible to obtain an artificial leather that has flexibility, and dense and soft-to-the-touch
surface quality.
[0038] In the present invention, the average single fiber diameter of ultrafine fiber is
calculated by taking a scanning electron microscope (SEM) photograph of a cross-section
of the artificial leather, randomly selecting 10 ultrafine fibers having a circular
shape or an elliptical shape close to a circular shape, measuring the single fiber
diameters, calculating the arithmetic average of the 10 fibers, and rounding the arithmetic
average off to the first decimal place. However, when ultrafine fibers having an irregular
cross-section are used, first, the cross-sectional area of the single fiber is measured,
and the diameter of a hypothetical circle on the assumption that the cross-section
was circular is calculated to obtain the diameter of the single fiber.
[0039] As the ultrafine fiber of the fiber entanglement constituting the artificial leather
of the present invention, various synthetic fibers including polyesters such as polyethylene
terephthalate, polytrimethylene terephthalate, polytetramethylene terephthalate, polycyclohexylenedimethylene
terephthalate, polyethylene-2,6-naphthalenedicarboxylate, and polyethylene-1,2-bis(2-chlorophenoxy)ethane-4,4'-dicarboxylate,
polyamides such as polyamide 6 and polyamide 66, polymers such as acrylic polyethylene
and polypropylene, and the like can be used. Among these, polyester fibers formed
of polymers such as polyethylene terephthalate, polybutylene terephthalate and polytrimethylene
terephthalate, and the like are excellent in strength, dimensional stability, light
resistance and coloring properties and are thus preferably used. Ultrafine fibers
formed of different materials can be mixed in the fiber entanglement as long as the
object of the present invention is not impaired.
[0040] The cross-sectional shape of the ultrafine fiber is circular from the viewpoint of
processing operability, and it is also possible to employ ultrafine fibers having
a modified cross-sectional shape such as an ellipse, polygons such as a flattened
polygon and a triangle, a fan shape, a cross shape, a hollow shape, a Y-shape, a T-shape,
and a U-shape.
[0041] Inorganic particles such as titanium oxide particles, a lubricant, a pigment, a thermal
stabilizer, a UV absorber, a conductive agent, a heat storage agent, an antibacterial
agent, and the like can be added to the ultrafine fibers forming the fiber entanglement
according to various purposes.
[0042] In order to achieve excellent deep color developability in the present invention,
a resin constituting the ultrafine fiber may be a polyester-based resin, and the polyester-based
resin may contain a pigment having an average particle diameter of 0.05 µm or more
and 0.20 µm or less. The particle diameter referred to herein is a particle diameter
in a state in which the pigment is present in the ultrafine fiber, and generally refers
to a particle diameter referred to as a secondary particle diameter. When the average
particle diameter is 0.05 µm or more, preferably 0.07 µm or more, the pigment is gripped
inside the ultrafine fiber, and therefore, falling off from the ultrafine fiber is
suppressed. When the average particle diameter is 0.20 um or less, preferably 0.18
um or less, more preferably 0.16 um or less, stability during spinning and yarn strength
are excellent. The average particle diameter is calculated by the following method.
- (1) An ultrathin slice having a thickness of 5 to 10 um is prepared in a cross-sectional
direction of a plane perpendicular to a longitudinal direction of the ultrafine fiber.
- (2) A fiber cross section in the ultrathin slice is observed with a transmission electron
microscope (TEM) at a magnification of 10,000.
- (3) Using image analysis software, an equivalent circle diameter of the particle diameter
of the pigment contained in a visual field of 2.3 um × 2.3 um of an observation image
is measured at 20 points. When the number of pigment particles contained in the visual
field of 2.3 um × 2.3 um is less than 20, the equivalent circle diameter of the particle
diameter of the existing pigment is all measured.
- (4) An average value (arithmetic average) is calculated for the particle diameters
at the measured 20 points.
[0043] In order to achieve excellent deep color developability in the present invention,
when the resin constituting the ultrafine fiber is a polyester-based resin and a pigment
is contained in the polyester-based resin, the content of the pigment contained in
the polyester-based resin forming the ultrafine fiber is preferably 0.5% by mass or
more and 2.0% by mass or less with respect to the mass of the ultrafine fiber. When
the proportion of the pigment is 0.5% by mass or more, preferably 0.7% by mass or
more, and more preferably 0.9% by mass or more, the deep color developability is excellent.
When the proportion of the pigment is 2.0% by mass or less, preferably 1.8% by mass
or less, and more preferably 1.6% by mass or less, an artificial leather having high
physical properties such as strength can be obtained. As the pigment, carbon-based
black pigments such as carbon black and graphite, and oxide-based black pigments such
as triiron tetraoxide and composite oxides of copper and chromium can be used. The
pigment is preferably carbon black from the viewpoint of easily obtaining a pigment
having a small particle diameter and excellent dispersibility in a polymer. As a chromatic
fine-particle oxide pigment, a known pigment close to the target color can be used,
and examples thereof include iron oxyhydroxide (e.g., "TM Yellow 8170" produced by
Dainichiseika Color & Chemicals Mfg. Co., Ltd.), iron oxide (e.g., "TM Red 8270" produced
by Dainichiseika Color & Chemicals Mfg. Co., Ltd.), and cobalt aluminate (e.g., "TM
Blue 3490E" produced by Dainichiseika Color & Chemicals Mfg. Co., Ltd.).
[0044] In the artificial leather of the present invention, a fiber entanglement including
the ultrafine fiber is one of constituent elements. Examples of the fiber entanglement
include a woven fabric, a knitted fabric, and a nonwoven fabric, and the fiber entanglement
further includes an elastomer inside or outside, and these may be properly used depending
on the cost and properties required for each application and purpose. Woven and knitted
fabrics are preferably used from the viewpoint of cost, and nonwoven fabrics, fiber
entanglements filled with an elastomer, and the like are preferably used from the
viewpoint of texture with a sense of fulfillment and quality due to fine naps.
[0045] In the case of using a woven/knitted fabric as the fiber entanglement, examples of
the woven fabric include plain woven fabrics, twill woven fabrics, satin woven fabrics,
and various woven fabrics based on these weave structures. As the knitted fabric,
any of warp knitted fabrics, weft knitted fabrics represented by tricot knit fabrics,
lace knit fabrics, and various knitted fabrics based on these knitting structures
may be adopted.
[0046] In the case of using a nonwoven fabric as the fiber entanglement, all nonwoven fabrics
described in various categories may be applied, such as general short fiber nonwoven
fabrics, long fiber nonwoven fabrics, needle punch nonwoven fabrics, papermaking nonwoven
fabrics, spunbond nonwoven fabrics, meltblown nonwoven fabrics, and electrospun nonwoven
fabrics. Here, a nonwoven fabric is preferable from the viewpoint of the texture with
a sense of fulfillment and the quality due to fine naps.
[0047] The inclusion of the elastomer inside or outside the fiber entanglement is more preferably
used from the viewpoint of excellent durability and abrasion resistance of the artificial
leather. In particular, it is preferable that the elastomer is contained in the fiber
entanglement from the viewpoint of flexibility.
[0048] In addition, in the artificial leather of the present invention, it is preferable
to integrate the fiber entanglement and a woven/knitted fabric (a) by entanglement
from the viewpoint of excellent mechanical strength. More preferably, the fiber entanglement
is a nonwoven fabric, and the woven/knitted fabric (a) is contained therein. Still
more preferably, a balance of appearance, flexibility, and strength is optimized when
the fiber entanglement is a nonwoven fabric and the woven/knitted fabric (a) is a
woven fabric.
[0049] In the woven/knitted fabric (a) integrated with the fiber entanglement, as the yarn
that constitutes the woven/knitted fabric (a), synthetic fibers formed of polyester,
polyamide, polyethylene, polypropylene, copolymers thereof, or the like are preferably
used. Among these, synthetic fibers formed of polyester, polyamide and copolymers
thereof may be used singly or in combination or in mixture. As the yarn that constitutes
the woven/knitted fabric (a), filament yarns, spun yarns, blended yarns of filaments
and short fibers, and the like may be used. From the viewpoint of durability, particularly
mechanical strength and the like, it is more preferable to use a multifilament including
a polyester-based resin or a polyamide-based resin.
[0050] When the average single fiber diameter of the fibers that constitute the woven/knitted
fabric (a) is 50.0 µm or less, more preferably 15.0 µm or less, and still more preferably
13.0 µm or less, not only an artificial leather excellent in flexibility is obtained,
but also even when the fibers of the woven/knitted fabric are exposed on the surface
of the artificial leather, a hue difference from the ultrafine fiber containing the
pigment after dyeing is reduced, so that uniformity of a hue of the surface is not
impaired. On the other hand, when the average single fiber diameter of the fibers
that constitute the woven/knitted fabric (a) is 1.0 µm or more, more preferably 8.0
µm or more, and still more preferably 9.0 µm or more, shape stability of a product
as an artificial leather is improved. The average single fiber diameter of the fibers
that constitute the woven/knitted fabric (a) is calculated by taking a scanning electron
microscope (SEM) photograph of the cross-section of the artificial leather, randomly
selecting 10 fibers constituting the woven fabric, measuring the single fiber diameter
of the fiber, calculating the arithmetic average of the 10 fibers, and rounding the
arithmetic average off to the first decimal place. When the fibers that constitute
the woven/knitted fabric (a) are multifilaments, a total fineness of the multifilaments
is measured according to "8.3.1 Fineness based on corrected mass b) Method B (simple
method)" in "8.3 Fineness" in JIS L 1013: 2010 "Chemical fiber filament yarn test
method", and is preferably 30 dtex or more and 170 dtex or less. When the total fineness
of the yarns that constitute the woven/knitted fabric (a) is 170 dtex or less, an
artificial leather excellent in flexibility is obtained. On the other hand, when the
total fineness is 30 dtex or more, not only the shape stability of a product as the
artificial leather is improved, but also when the fiber entanglement is a nonwoven
fabric, the fibers that constitute the woven/knitted fabric (a) are less likely to
be exposed on the surface of the artificial leather when the woven/knitted fabric
(a) is integrated by entanglement by needle punching or the like, which is preferable.
When the woven/knitted fabric (a) is a woven fabric, the multifilaments of the warp
and the weft preferably have the same total fineness. In addition, the yarns constituting
the woven fabric preferably have a twist count of 1000 T/m or more and 4000 T/m or
less. When the twist count is 4000 T/m or less, more preferably 3500 T/m or less,
and still more preferably 3000 T/m or less, an artificial leather excellent in flexibility
is obtained. When the twist count is 1000 T/m or more, more preferably 1500 T/m or
more, and still more preferably 2000 T/m or more, in a case where a nonwoven fabric
and a woven fabric are integrated by entanglement by needle punching or the like,
damage to fibers constituting the woven fabric can be prevented, and the mechanical
strength of the artificial leather is excellent, which is preferable.
[0051] As the woven/knitted fabric (a), a woven/knitted fabric containing a composite fiber
(hereinafter, described as a side-by-side composite fiber in some cases) in which
two or more kinds of polymers are combined in a side-by-side or eccentric sheath-core
type may also be used. For example, in a side-by-side composite fiber formed of two
or more kinds of polymers having different intrinsic viscosities (IV), different internal
strains are generated between the two components by stress concentration on the high
viscosity side during stretching. Because of this internal strain, the high viscosity
side shrinks greatly by the difference in elastic recovery after stretching and the
difference in thermal shrinkage in the heat treatment process, and strain is generated
in the single fiber to develop a three-dimensional coil type crimp. By this three-dimensional
coil type crimp, stretchability as artificial leather is developed.
[0052] When the fiber entanglement is a nonwoven fabric, a nonwoven fabric can provide an
appearance and a texture that are uniform and elegant when the surface of the nonwoven
fabric is napped. Examples of the form of the nonwoven fabric include a long fiber
nonwoven fabric mainly composed of filaments and a short fiber nonwoven fabric mainly
composed of fibers of 100 mm or less. When the long fiber nonwoven fabric is used
as a fibrous substrate, an artificial leather having excellent strength can be obtained,
which is preferable. On the other hand, in the case of the short fiber nonwoven fabric,
the number of fibers oriented in the thickness direction of the artificial leather
can be increased as compared with the case of the long fiber nonwoven fabric, and
the surface of the artificial leather when napped can have a high dense feeling.
[0053] The fiber length of the ultrafine fibers in the case where a short fiber nonwoven
fabric is used is preferably 25 mm or more and 90 mm or less. When the fiber length
is 90 mm or less, more preferably 80 mm or less, and still more preferably 70 mm or
less, good quality and texture are obtained. On the other hand, when the fiber length
is 25 mm or more, more preferably 35 mm or more, and still more preferably 40 mm or
more, an artificial leather with excellent abrasion resistance can be obtained.
[0054] The basis weight of the fiber entanglement including the ultrafine fiber that constitutes
the artificial leather according to the present invention is measured according to
"6.2 Mass per Unit Area (ISO method)" in "Test methods for nonwovens" of JIS L 1913:
2010, and is preferably in a range of 50 g/m
2 or more and 600 g/m
2 or less. When the basis weight of the nonwoven fabric is 50 g/m
2 or more, more preferably 100 g/m
2 or more, an artificial leather having a sense of fulfillment and an excellent texture
can be obtained. On the other hand, when the basis weight is 600 g/m
2 or less, more preferably 450 g/m
2 or less, a soft artificial leather having excellent moldability can be obtained.
Even when the woven/knitted fabric (a) is integrated by entanglement, the basis weight
of the fiber entanglement is preferably in the above-described basis weight range.
[Elastomer]
[0055] Next, the artificial leather of the present invention has an elastomer. Preferably,
the elastomer is contained in the fiber entanglement. By including the elastomer inside,
the softness, shape stability, and abrasion resistance of the artificial leather are
improved. Unlike a functional agent (flame retardant or the like) to be described
later, the elastomer is required to have a purpose as a binder of the fiber entanglement.
[0056] As the elastomer, polyurethane, styrene-butadiene rubber (SBR), nitrile rubber (NBR),
acrylic resin, and the like may be used, and it is a preferred aspect to use polyurethane
as the main component among these. Use of polyurethane can afford an artificial leather
having touch having feels like natural suede, an elegant appearance, and physical
properties enough to endure actual use.
[0057] The polyurethane forming the elastomer preferably contains a black pigment (b) having
an average particle diameter of 0.05 um or more and 0.20 um or less and a coefficient
of variation (CV) of 75% or less.
[0058] The particle diameter referred to herein is a particle diameter in a state in which
the black pigment (b) is present in the elastomer, and generally refers to a particle
diameter referred to as a secondary particle diameter.
[0059] When the average particle diameter is 0.05 µm or more, preferably 0.07 µm or more,
the black pigment (b) is gripped inside the elastomer, and therefore, falling off
from the ultrafine fiber is suppressed. When the average particle diameter is 0.20
µm or less, preferably 0.18 um or less, more preferably 0.16 µm or less, dispersibility
is excellent when the elastomer is impregnated.
[0060] When the coefficient of variation (CV) of the particle diameter is 75% or less, preferably
65% or less, more preferably 60% or less, still more preferably 55% or less, and most
preferably 50% or less, a distribution of the particle diameter becomes small, and
falling off of small particles from a surface of the elastomer, precipitation of significantly
aggregated particles in an impregnation tank, and the like are suppressed.
[0061] In the present invention, the average particle diameter and the coefficient of variation
(CV) are calculated by the following method.
- (1) An ultrathin slice having a thickness of 5 to 10 um is prepared in a cross-sectional
direction of a plane perpendicular to a longitudinal direction of the artificial leather.
- (2) A cross section of the elastomer in the ultrathin slice is observed with a transmission
electron microscope (TEM) at a magnification of 10,000.
- (3) Using image analysis software, an equivalent circle diameter of the particle diameter
of the black pigment (b) contained in a visual field of 2.3 µm × 2.3 µm of an observation
image is measured at 20 points. When the number of particles of the black pigment
(b) contained in the visual field of 2.3 µm × 2.3 µm is less than 20, the equivalent
circle diameter of the particle diameter of the existing black pigment (b) is all
measured.
- (4) The average value (arithmetic average) and the coefficient of variation (CV) are
calculated for the particle diameters at the measured 20 points. In the present invention,
the coefficient of variation is calculated by the following equation:

[0062] As the black pigment (b) in the present invention, carbon-based black pigments such
as carbon black and graphite, and oxide-based black pigments such as triiron tetraoxide
and composite oxides of copper and chromium can be used. The black pigment is preferably
carbon black from the viewpoint of easily obtaining a pigment having a small particle
diameter and excellent dispersibility in a polymer.
[0063] As the polyurethane used in the present invention, either organic solvent-based polyurethane
used in the state of being dissolved in an organic solvent or water-dispersible polyurethane
used in the state of being dispersed in water can be used. Polyurethane obtained by
reaction of a polymer diol, an organic diisocyanate, and a chain extender is preferably
used as polyurethane to be used for the present invention.
[0064] For example, a polycarbonate-based diol, polyester-based diol, polyether-based diol,
silicone-based diol, or fluorine-based diol can be used as the aforementioned polymer
diol, and a copolymer of a combination of these diols can also be used. Among them,
it is a preferred aspect to use a polycarbonate-based diol from the viewpoint of hydrolysis
resistance and abrasion resistance.
[0065] A polycarbonate-based diol as described above can be produced, for example, through
ester exchange reaction between alkylene glycol and ester carbonate or through reaction
of phosgene or a chloroformate with alkylene glycol.
[0066] Examples of the alkylene glycol include linear alkylene glycols such as ethylene
glycol, propylene glycol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, 1,9-nonanediol,
and 1,10-decanediol, branched alkylene glycols such as neopentyl glycol, 3-methyl-1,5-pentanediol,
2,4-diethyl-1,5-pentanediol, and 2-methyl-1,8-octanediol, alicyclic diols such as
1,4-cyclohexanediol, aromatic diols such as bisphenol A, and glycerin, trimethylolpropane,
and pentaerythritol. In the present invention, either a polycarbonate-based diol obtained
from a single alkylene glycol or a copolymerized polycarbonate-based diol obtained
from two or more alkylene glycols can be adopted.
[0067] Examples of the polyester-based diols include polyester diols produced by condensing
one of various low molecular weight polyols and a polybasic acid.
[0068] For example, one or a plurality selected from the following can be used as the low
molecular weight polyol described above: ethylene glycol, 1,2-propylene glycol, 1,3-propylene
glycol, 1,3-butane diol, 1,4-butane diol, 2,2-dimethyl-1,3-propane diol, 1,6-hexane
diol, 3-methyl-1,5-pentane diol, 1,8-octane diol, diethylene glycol, triethylene glycol,
dipropylene glycol, tripropylene glycol, cyclohexane-1,4-diol, and cyclohexane-1,4-dimethanol.
[0069] Adducts prepared by adding various alkylene oxides to bisphenol A are also usable.
[0070] Furthermore, for example, one or a plurality selected from the following can be used
as the polybasic acid: succinic acid, maleic acid, adipic acid, glutaric acid, pimelic
acid, suberic acid, azelaic acid, sebacic acid, dodecane dicarboxylic acid, phthalic
acid, isophthalic acid, terephthalic acid, and hexahydroisophthalic acid.
[0071] Examples of the polyether-based diols used in the present invention include polyethylene
glycol, polypropylene glycol, polytetramethylene glycol, and copolymerized diols which
are formed by combining these substances.
[0072] The number average molecular weight of the polymer diol is preferably in a range
of 500 or more and 4000 or less when the molecular weight of a polyurethane-based
elastomer is constant. When the number average molecular weight is preferably 500
or more, more preferably 1,500 or more, it is possible to prevent the artificial leather
from becoming hard. When the number average molecular weight is 4000 or less, or more
preferably 3000 or less, the polyurethane can maintain its strength.
[0073] Examples of the organic diisocyanate used in the present invention include aliphatic
diisocyanates such as hexamethylene diisocyanate, dicyclohexylmethane diisocyanate,
isophorone diisocyanate, and xylylene diisocyanate, and aromatic diisocyanates such
as diphenylmethane diisocyanate and tolylene diisocyanate. These compounds can also
be used in combination.
[0074] As the chain extender, amine chain extenders such as ethylenediamine and methylenebisaniline,
and diol chain extenders such as ethylene glycol can be preferably used. Furthermore,
a polyamine which is obtained by reacting polyisocyanate and water can also be used
as a chain extender.
[0075] The polyurethane used in the present invention may be used in combination with a
crosslinker with the aim of improving waterproofness, abrasion resistance, hydrolysis
resistance, and the like. The crosslinker may be an external crosslinker that is added
as a third component to polyurethane, or an internal crosslinker that introduces reaction
points to form a crosslinked structure in advance into the polyurethane molecular
structure. It is preferable to use an internal crosslinker from the viewpoint that
crosslinking points can be formed more uniformly in the polyurethane molecular structure
and that the decrease in flexibility can be mitigated.
[0076] The crosslinking agent used may be a compound having an isocyanate group, an oxazoline
group, a carbodiimide group, an epoxy group, a melamine resin, a silanol group and
the like.
[0077] The elastomer may contain various additives including flame retardants such as "phosphorus,
halogen, and inorganic flame retardants"; antioxidants such as "phenolic, sulfur,
and phosphorus antioxidants"; ultraviolet absorbers such as "benzotriazole, benzophenone,
salicylate, cyanoacrylate, and oxalic acid anilide UV absorbers"; light stabilizers
such as "hindered amine and benzoate light stabilizers"; hydrolysis stabilizers such
as polycarbodiimide; plasticizers; antistatic agents; surfactants; coagulation modifiers;
and dyes according to purposes.
[0078] In general, the content of the elastomer in the artificial leather can be appropriately
adjusted in consideration of the type of the elastomer to be used, a production method
for the elastomer, and the texture and physical properties; however, in the present
invention, the content of the elastomer is preferably 10% by mass or more and 60%
by mass or less with respect to the mass of the fiber entanglement. When the content
of the elastomer is preferably 10% by mass or more, more preferably 15% by mass or
more, still more preferably 20% by mass or more, the bonding between the fibers by
the elastomer can be enhanced, and the abrasion resistance of the artificial leather
can be improved. On the other hand, when the content of the elastomer is preferably
60% by mass or less, more preferably 45% by mass or less, still more preferably 40%
by mass or less, the flexibility of the artificial leather can be further increased.
[0079] According to a preferred aspect of the artificial leather of the present invention,
the density of the fiber entanglement including the elastomer, that is, the density
of the fiber entanglement with the elastomer (the density of the woven/knitted fabric
(b) described later and the artificial leather containing no flame retardant) is preferably
0.20 g/cm
3 or more and 0.50 g/cm
3 or less. When the density is 0.20 g/cm
3 or more, preferably 0.25 cm
3, the shape stability, dimensional stability, and strength of the artificial leather
become sufficient. In addition, the artificial leather becomes dense, and the opening
portion becomes a clean opening portion without fraying or the like. On the other
hand, when the density is 0.50 g/cm
3 or less, preferably 0.45 g/cm
3 or less, the air permeability and flexibility of the artificial leather are improved.
[Functional agent (flame retardant or the like)]
[0080] The functional agent used in the present invention refers to an agent that imparts
functionality such as flame retardancy, antifouling properties, yellowing resistance,
NOx resistance, grip properties, water repellency, oil repellency, color migration
resistance, abrasion resistance, odor resistance, durability, flexibility, and stretchability
to a fibrous product. The functional agent (flame retardant or the like) used for
the artificial leather of the present invention has tackiness of 0.1 N/cm
2 or more and 2.0 N/cm
2 or less. When the tackiness of the functional agent (flame retardant or the like)
is 0.10 N/cm
2 or more, preferably 0.15 N/cm
2 or more, and more preferably 0.20 N/cm
2 or more, the functional agent (flame retardant or the like) is secured to the fiber
entanglement with sufficient adhesiveness during application and drying of the functional
agent (flame retardant or the like), and the functional agent (flame retardant or
the like) after drying does not fall off even in a high-temperature environment. When
the tackiness is 2.00 N/cm
2 or less, preferably 1.60 N/cm
2 or less, and more preferably 1.00 N/cm
2 or less, after the formation of the opening, the fiber dusts composed of the fiber,
the elastomer, and the functional agent (flame retardant or the like) are not clogged
in the opening, and the formability of the opening portion is improved, and when the
formation of the opening portion is punching, continuous processing can be performed
without clogging the needle hole. In addition, a structure in which the functional
agent (flame retardant or the like) is uniformly dispersed and bonded is obtained,
and the texture of the artificial leather becomes flexible. In the present invention,
the tackiness of the functional agent (flame retardant or the like) is a value obtained
by measurement and calculation as follows.
- (1) A functional agent (flame retardant or the like) is heated to 60°C.
- (2) Using a tack meter, a stainless steel probe (contact pressure 24.5 N/cm2) is pressed against the functional agent (flame retardant or the like) at a speed
of 6 mm/min, and held for 5 seconds.
- (3) After (2), a maximum load at the time of peeling at 6 mm/min is read.
- (4) (2) to (3) are repeated five times, and the arithmetic average of the resulting
values is rounded off to the second decimal place.
[0081] In order to stably obtain the adhesiveness, opening properties, and softness even
when there is a temperature change, the tackiness when the functional agent (flame
retardant or the like) is heated to 40°C is preferably 0.05 N/cm
2 or more and 1.00 N/cm
2 or less, and the tackiness at 20°C is preferably 0.01 N/cm
2 or more and 0.50 N/cm
2 or less. In particular, the tackiness at 20°C is preferable when the stickiness of
the surface of the functional surface (surface of the flame retardant or the like)
is small as handleability such as molding or sewing of an artificial leather sheet
at room temperature. When the tackiness of the functional agent is within the above
range, resistance is reduced when the artificial leather is unwound from the roll
shape, and the handleability of the artificial leather is improved in the work of
the next step. When the functional agent (flame retardant or the like) is heated to
40°C or 20°C, the tackiness is measured in the same manner as described above except
that the heating temperature in (1) is changed to 40°C or 20°C.
[0082] Although the functional agent (flame retardant or the like) may be a resin itself
composed of a polymer compound having an active functional group, in addition to a
low molecular compound having a functional component (flame retardant component or
the like), it is preferable to contain a resin in order to obtain durability of functionality,
and the resin is selected from, for example, an acrylic resin, a urethane resin, a
polyester resin, a vinyl acetate resin, and the like, is not particularly limited,
and is preferably an acrylic resin having a good balance from the viewpoint of adhesiveness
to a fiber entanglement and a woven/knitted fabric, heat resistance, and adhesiveness.
An amount of the binder resin to be blended is not limited to a specific value, and
is preferably in a range of 5 to 50% by mass with respect to a total mass of the functional
component (flame retardant component or the like) contained in the functional agent
(flame retardant or the like). When the blending amount is 5% by mass or less, the
flame retardant is likely to cause falling off of a powder component, and when the
blending amount exceeds 50% by mass, the texture of the artificial leather may be
impaired. From the viewpoint of the tackiness, for example, a resin having low rubber
elasticity is preferably used. For example, regarding the acrylic resin, an acrylamide-based
acrylic resin is more preferable than an acrylonitrile-based acrylic resin because
the tackiness is better. In general, many resins have a hard texture, and the texture
can be softened by reducing the blending amount of the resin. When an ethylene-vinyl
acetate resin having high adhesiveness is used, the adhesiveness and the tackiness
are enhanced even in a small amount; therefore, when it is desired to reduce the blending
amount of the resin, it is preferable to contain ethylene-vinyl acetate.
[0083] When the functional agent is a flame retardant and a combustion mode is a carbonization
type, as the resin of the flame retardant, other resins such as acrylic resins, SBR
resins, and MBR resins may also be used, provided they do not affect the carbide formation
of vinyl acetate, vinyl acetate copolymer resins, or the like. In particular, if the
flame retardant is made to further include an acrylic resin, the advantages of softened
texture and improved water resistance of the flame retardant are obtained.
[0084] The type of the flame retardant component of the flame retardant is not particularly
limited, and the flame retardant component is preferably water-insoluble or sparingly
water-soluble from the viewpoint of water spot. The "water spot" as used herein refers
to a phenomenon in which, in the artificial leather to which a flame retardant is
added, when moisture typified by water droplets adheres from either side of the front
and back surfaces and the artificial leather is then naturally dried, the wet portion
becomes a white spot or stain. From the viewpoint of adapting to recent environmental
hormone regulations, it is preferable to use a dehalogenated flame retardant. Examples
of the dehalogenated flame retardant include phosphorus-containing compounds, nitrogen-containing
compounds, phosphorus-nitrogen compounds, sulfoamide-based compounds, phosphorus-sulfoamide-based
compounds, and sulfur-containing nitrogen-based compounds, and these can be used alone
or in combination of two or more thereof. From the viewpoint of the flame retardant
performance, a phosphorus-based compound is preferable, and examples of the phosphorus-based
compound include guanidine-based compounds, carbamate-based compounds, phosphate ester-based
compounds, phosphate ester-amide-based compounds, ammonium polyphosphate compounds,
and aromatic phosphate ester-based compounds such as triphenyl phosphate and trixylenyl
phosphate. Particularly, an ammonium polyphosphate flame retardant having a high phosphorus
content is preferable, and a type covered with a melamine resin or a silicon oxide
resin is preferable for further making the flame retardant sparingly water-soluble.
As the inorganic flame retardant, known flame retardants such as aluminum hydroxide,
titanium oxide, zinc oxide, expandable graphite, magnesium hydroxide, calcium carbonate,
zinc borate, ammonium polyphosphate, and red phosphorus can be used, and it is preferable
to use a polyphosphate-based flame retardant excellent in processability and durability.
[0085] As the combustion mode of the flame retardant, there are a carbonization type for
forming a carbonized film and a melting type for dropping a fire source, and although
any mode is not limited, the melting type is preferable from the viewpoint of flame
retardant stability in flame retardant evaluation in the case of sufficient flame
retardancy.
[0086] In the artificial leather of the present invention, in the evaluation of the flame
retardancy, based on burning test standard (horizontal burning rate) of automobile
interior material of Federal Motor Vehicle Safety Standards (FMVSS) No. 302, a test
piece (350 mm × 100 mm) is held horizontally, a 38 mm flame is allowed to remain for
15 seconds, and the flame retardancy is evaluated by a burning rate with respect to
254 mm between a gauge line A and a gauge line B according to the following criteria.
- In the case where the flame self-extinguishes before reaching the gauge line A, a
judgment classification is "non-combustible", and the product is judged as acceptable.
- In the case where the flame self-extinguishes after the gauge line A, and the burning
distance is within 50 mm and the burning time was within 60 seconds, the judgment
classification is "self-extinguished", and the product is judged as acceptable.
- In the case where the flame does not self-extinguish but the burning rate between
the gauge lines is 4 inches/min (about 101.6 mm/min) or less, the judgment classification
is "burning at rate not more than specified rate", and the product is judged as acceptable.
- In the case where the flame does not self-extinguish and the burning rate between
the gauge lines exceeds 4 inches/min (about 101.6 mm/min), the judgment classification
is "burning at rate exceeding specified rate", and the composite sheet product is
judged as unacceptable.
[0087] For example, when a carbonization type agent such as an antifouling agent is applied
to the artificial leather, since the flame retardant is of the carbonization type,
the carbonization amount increases, the flame retardancy improves, and the combustion
mode can be selected according to the material configuration of the artificial leather.
When the carbonization type is selected for the flame retardant, by selecting a resin
that is easily carbonized for the resin of the flame retardant, the above-described
flame retardant component can be reduced, which is preferable from the viewpoint of
cost. For example, there is a vinyl group-containing resin that forms a carbonized
skeleton during combustion.
[0088] It is preferable that the vinyl group-containing resin contains at least one selected
from a vinyl acetate resin, an ethylene-vinyl acetate copolymer resin, an acrylic
vinyl acetate copolymer resin, a vinyl acetate vinyl copolymer resin, and a branched
fatty acid vinyl acetate copolymer resin, since the formation of a carbide by using
the vinyl acetate resin or the vinyl acetate copolymer resin in combination with a
phosphorus-based compound promotes flame retardancy, and particularly exhibits an
effect of improving flame retardant properties for horizontal burning of the artificial
leather.
[0089] An adhesion amount of the flame retardant is required to be determined from the viewpoint
of securing necessary flame retardant performance and reducing texture curing, and
increases or decreases depending on the basis weight, thickness, and ultrafine fiber
of the artificial leather, the polymer type of the elastomer, and the fiber entanglement
type; however, it is preferable to contain the flame retardant in an amount of 2 to
30% by mass with respect to the artificial leather from the viewpoint of achieving
both the flame retardancy and the texture. An application amount of the flame retardant
is preferably 10 to 200 g/m
2, and more preferably within a range of 20 to 100 g/m
2. Although the adhesion amount of the flame retardant can be calculated by, for example,
mass after application - mass after application, when the adhesion amount is calculated
from the artificial leather after application, the adhesion amount can also be calculated
using elemental peak analysis such as fluorescent X-rays.
[0090] As a solution used for applying the flame retardant to the artificial leather, it
is preferable that the viscosity is 500 to 10000 mPa·s at normal temperature from
the viewpoint of coating permeability, and a viscosity modifier may be contained as
necessary. The viscosity is more preferably 1500 to 9000 mPa-s, and still more preferably
2500 to 7000 mPa·s. In this way, a presence ratio of the flame retardant described
later in the thickness direction falls within a suitable range, and an artificial
leather that is more flexible and has high flame retardancy can be obtained. The method
for measuring the viscosity of the solution is not particularly limited, but a measurement
method using a commonly used rotational viscometer is used. The viscosity modifier
used for adjusting the viscosity of the solution is preferably poorly soluble in water
from the viewpoint of preventing occurrence of water spot, and is preferably, for
example, an alkali-thickened acrylic resin or an ethylene oxide higher fatty acid
ether.
[0091] In the present invention, in addition to the components described above, aluminum
hydroxide, magnesium hydroxide, a metal oxide, and the like can also be used as a
flame retardant aid for the flame retardant.
[0092] The adhesion amount of the functional agent (flame retardant or the like) is required
to be determined from the viewpoint of securing necessary functional performance and
reducing texture curing, and the opening properties of the artificial leather backing
material, and increases or decreases depending on the basis weight, thickness, and
ultrafine fiber of the artificial leather, the polymer type of the elastomer, and
the fiber entanglement type; however, it is preferable to contain the functional agent
in an amount of 2 to 30% by mass with respect to the artificial leather from the viewpoint
of satisfying the above characteristics. An application amount of the functional agent
(flame retardant or the like) is preferably 10 to 200 g/m
2, and more preferably within a range of 20 to 100 g/m
2.
[Woven/knitted fabric (b)]
[0093] In the artificial leather of the present invention, the functional surface (surface
of flame retardant or the like) is preferably a surface formed by stacking the woven/knitted
fabric (b). That is, by adopting an aspect in which the woven/knitted fabric (b) is
further stacked to the fiber entanglement on the functional surface (surface of flame
retardant or the like) side opposite to the napped surface of the artificial leather,
the artificial leather has more strength and also has flexibility. In this case, the
fiber entanglement may include the woven/knitted fabric (a) as described above, and
a suitable woven/knitted fabric can be selected according to the purpose of each of
the woven/knitted fabric (a) and the woven/knitted fabric (b).
[0094] As for the kind of the woven/knitted fabric (b) used in the present invention, it
is possible to use any of various kinds of knitted fabrics such as warp knitted fabrics
and weft knitted fabrics typified by tricot knitted fabrics, lace knitted fabrics,
and knitted fabrics based on these knitting methods, and various kinds of woven fabrics
such as plain weave fabrics, twill weave fabrics, satin weave fabrics, and woven fabrics
based on these weaving methods. In a preferred aspect, a knitted fabric having high
air permeability and high stretchability is used as the woven/knitted fabric (b).
[0095] As for the kind of the yarn that constitutes the woven/knitted fabric (b), for example,
a filament yarn, a spun yarn, or a blended yarn of a filament yarn and short fibers
can be used.
[0096] The density of the woven/knitted fabric (b) is preferably 0.10 g/cm
3 or more and 0.60 g/cm
3 or less. When the density of the woven/knitted fabric (b) is 0.10 g/cm
3 or more, more preferably 0.15 g/cm
3 or more, an artificial leather having good shape retention can be obtained. On the
other hand, when the density of the woven/knitted fabric (b) is 0.60 g/cm
3 or less, more preferably 0.50 g/cm
3 or less, the functional agent (flame retardant or the like) can be penetrated to
the inside, and an artificial leather excellent in flexibility can be obtained.
[0097] The thickness of the woven/knitted fabric (b) is preferably 0.10 to 2.50 mm, more
preferably 0.15 to 1.50 mm, and still more preferably 0.20 to 1.00 mm. If the thickness
of the woven/knitted fabric (b) is less than 0.10 mm, the processability and strength
at the time of sticking with the fiber entanglement are deteriorated, and if the thickness
exceeds 2.50 mm, the flexibility of the air permeability tends to be impaired.
[0098] The method of stacking the fiber entanglement and the woven/knitted fabric (b) is
not limited, and a method of bonding the fiber entanglement and the woven/knitted
fabric (b) with an adhesive interposed therebetween is common. Examples of the adhesive
include thermoplastic resins such as a polyester resin, a copolymerized polyester
resin, a nylon resin, and an acrylic resin, and moisture-curable resins such as a
silicone rubber, a polystyrene rubber, and a polyurethane resin. A thermoplastic resin
excellent in workability is preferably used and, in particular, a nylon resin excellent
in hydrolysis resistance is preferably used. In the artificial leather including the
ultrafine fiber, a moisture-curable resin capable of being processed with a low thermal
history is preferable from the viewpoint of improving rubbing fastness.
[0099] A thickness of an adhesive layer is preferably 1 to 300 um as long as the adhesive
layer has sufficient bondability and does not impair the flexibility and air permeability
of the artificial leather.
[0100] In the case where a thermoplastic resin is used as the adhesive, the softening temperature
of the thermoplastic resin is preferably 70 to 160°C, more preferably 80 to 120°C.
If the softening temperature is lower than 70°C, the thermoplastic resin may be softened
during the processing or actual use. If the softening temperature is higher than 160°C,
the texture of the artificial leather and the rubbing fastness may be impaired by
the softening treatment at the time of sticking.
[Artificial leather]
[0101] The artificial leather of the present invention includes the fiber entanglement and
the elastomer, and one surface is a napped surface having a raised nap, and the other
surface is a flame retardant surface having the flame retardant.
[0102] First, in the artificial leather of the present invention, one surface is the napped
surface having the raised nap. That is, the raised nap may be provided only on the
surface to be a product surface of the artificial leather, and is also allowed to
be provided on both surfaces. As for the form of raised nap in the case where the
artificial leather has raised nap on the surface to be the product surface, the raised
nap preferably has a length and direction flexibility to such an extent that traces
remain when the artificial leather is stroked with a finger, that is, a so-called
finger mark remain due to the change of direction of the raised nap from the viewpoint
of design effects. Examples of the form having raised nap on the other surface (back
surface) with respect to the product surface of the artificial leather include imparting
a flame retardant after forming raised nap on the back surface of the fiber entanglement.
When the woven/knitted fabric (b) is stacked on the back surface of the fiber entanglement,
the front and back surfaces of the fiber entanglement are napped, and the flame retardant
is added to the surface of the stacked woven/knitted fabric (b), so that the flame
retardant is present in the napped portion of the back surface of the fiber entanglement,
and the flame retardant surface has raised nap.
[0103] More specifically, when the surface to be the product surface is the napped surface,
the raised napped length on the surface is preferably 50 um or more and 500 um or
less, and more preferably 100 um or more and 450 um or less. When the raised nap length
is 50 um or more, the raised nap covers the elastomer, and the exposure of the elastomer
on the product surface of the artificial leather is suppressed, so that an elegant
appearance can be obtained. When the woven/knitted fabric (a) is entangled and integrated
with the fiber entanglement constituting the artificial leather, or when the fiber
entanglement itself includes a woven/knitted fabric, setting the raised nap length
within the above range can sufficiently cover a tissue of the woven/knitted fabric
in the vicinity of the product surface of the artificial leather, which is preferable
in that a naturally-like and elegant appearance can be obtained. On the other hand,
when the raised nap length is 500 um or less, an artificial leather excellent in design
effect and abrasion resistance can be obtained.
[0104] In the present invention, the raised nap length of the artificial leather is calculated
by the following method.
- (1) A thin slice with a thickness of 1 mm in the cross-sectional direction of a plane
perpendicular to the longitudinal direction of the artificial leather is prepared
in the state of the raised nap of the artificial leather being ruffled by using a
lint brush, etc.
- (2) A cross-section of the artificial leather is observed at 90-fold magnification
by means of a scanning electron microscope (SEM).
- (3) In an SEM image photographed, the height of a raised nap portion (layer including
only ultrafine fiber) is measured at 10 points at intervals of 200 um in the width
direction of the cross-section of the artificial leather.
- (4) With respect to the measured height of the raised nap portion (layer including
only ultrafine fiber) at 10 points, the average value (arithmetic average) is calculated.
[0105] In the artificial leather of the present invention, it is important to have a plurality
of opening portions in the functional surface (surface of flame retardant or the like).
The "opening portion" in the present invention is not limited to a portion where a
hole (through opening portion) formed by penetrating an artificial leather from the
napped surface to the functional surface (surface of flame retardant or the like)
is opened, and includes, for example, a case where the opening portion does not overlap
the woven/knitted fabric (b) in a planar direction and is not the through opening
portion. Examples of the latter include a form in which an opening portion is formed
in advance in the woven/knitted fabric (b) containing the functional agent (flame
retardant or the like) and the woven/knitted fabric (b) is stacked on the fiber entanglement.
The shape of the opening portion can be any shape according to a desired design, and
polygonal shapes such as a round shape, an elliptical shape, a flat shape, and a triangular
shape, a fan shape, a cross shape, and deformed shapes such as a hollow shape, a Y
shape, a T shape, and a U shape can be adopted. An arrangement pattern of the opening
portion is not particularly limited, and the opening portion may be regularly provided
or irregularly provided; however, from the viewpoint of exhibiting uniform air permeability
and strength throughout the artificial leather, the opening portions are preferably
regularly arranged at predetermined intervals. A hole diameter of the opening portion
is preferably 0.1 to 3.0 mm and more preferably 0.5 to 2.5 mm from the viewpoint of
achieving both air permeability and strength of the entire artificial leather.
[0106] In addition, in the artificial leather of the present invention, an opening ratio
of the functional surface (surface of flame retardant or the like) is preferably 1%
or more and 40% or less from the viewpoint of achieving both air permeability and
strength of the entire artificial leather. That is, when the opening ratio is 1% or
more, more preferably 2% or more, an artificial leather excellent in air permeability
can be obtained. On the other hand, when the opening ratio is 40% or less, more preferably
20% or less, and still more preferably 150 or less, an artificial leather excellent
in strength can be obtained.
[0107] The artificial leather of the present invention has a plurality of opening portions
in each of the napped surface and the functional surface (surface of flame retardant
or the like), and at least some of the opening portions are the through opening portions
formed to penetrate from the napped surface to the functional surface (surface of
flame retardant or the like). With this configuration, an artificial leather having
more excellent air permeability can be obtained.
[0108] The shape of the through opening portion in the thickness direction may be, for example,
a cylindrical through opening portion in which the hole diameters of the opening portion
of the napped surface and the opening portion of the functional surface (surface of
flame retardant or the like) are the same, or a mortar-shaped through opening portion
in which the hole diameters of the opening portion of the napped surface and the opening
portion of the functional surface (surface of flame retardant or the like) are different.
That is, the shape of the through opening portion can be selected in consideration
of the design and mechanical properties of the artificial leather.
[0109] In the artificial leather of the present invention, the presence ratio of the functional
agent (flame retardant or the like) in the thickness direction preferably satisfies
the following formula:

where W is the thickness (mm) from the functional surface (surface of flame retardant
or the like) where the functional agent (flame retardant or the like) is present,
and W
0 is the thickness (mm) of the entire artificial leather. When the presence ratio of
the functional agent (flame retardant or the like) in the thickness direction is 0.001
or more, more preferably 0.01 or more, still more preferably 0.05 or more, an artificial
leather excellent in functionality (flame retardancy or the like) can be obtained.
On the other hand, when the presence ratio of the functional agent (flame retardant
or the like) in the thickness direction is 0.7 or less, more preferably 0.5 or less,
and still more preferably 0.3 or less, an artificial leather excellent in air permeability
and flexibility can be obtained.
[0110] The presence ratio of the functional agent (flame retardant or the like) in the
thickness direction is obtained by collecting and preparing three SEM measurement
samples, randomly selecting five points in an observation image of each cross section,
measuring W and W
0 at each point, and calculating W/W
0 using an arithmetic average value. When the functional agent (flame retardant or
the like) cannot be specified from a normal SEM image, for example, calculation is
performed using a method of determining a resin containing an element peak as the
functional agent by SEM-EDX. For example, in the case of the flame retardant, calculation
is performed using a method of determining a resin containing a phosphorus element
peak as the flame retardant.
[0111] As a preferred form of the artificial leather, a form in which the woven/knitted
fabric (b) is stacked on the fiber entanglement and the functional agent (flame retardant
or the like) is unevenly distributed in the woven/knitted fabric (b) is preferable
from the viewpoint of functionality (flame retardancy or the like).
[0112] As a preferable form of the functional surface (surface of flame retardant or the
like) of the artificial leather, it is preferable that the functional agent (flame
retardant or the like) is present on the surface of the functional surface (surface
of flame retardant or the like), and an area ratio of the functional agent (flame
retardant or the like) of the functional surface (surface of flame retardant or the
like) is 10 to 100%. The area ratio is obtained by collecting and preparing three
SEM measurement samples, randomly selecting five points in an observation image of
50 times of the surface of each functional surface (surface of flame retardant or
the like), photographing a SEM image, binarizing the SEM image, and then performing
calculation by using a value obtained by arithmetically averaging the area ratio in
which the functional agent (flame retardant or the like) is present with respect to
a total area obtained by excluding the opening portion from an image area of 50 times.
When the area ratio is preferably 10% or more, more preferably 30% or more, an artificial
leather excellent in functionality (flame retardancy or the like) and functional (flame
retardant, etc.) stability can be obtained, and for example, when a polyurethane foam
is laminated on the back surface of an artificial leather such as an interior material
for vehicles, smoothness of the functional surface (surface of flame retardant or
the like) increases, so that e peel strength with the polyurethane foam increases.
[0113] The artificial leather of the present invention preferably has a thickness of 0.2
mm or more and 2.5 mm or less as measured according to "6.1.1 A method" in "6.1 Thickness
(ISO method)" in "Test methods for nonwovens" of JIS L 1913: 2010 When the thickness
of the artificial leather is 0.2 mm or more, more preferably 0.3 mm or more, and still
more preferably 0.4 mm or more, not only excellent processability at the time of production
is obtained, but also a sense of fulfillment and excellent texture are obtained. On
the other hand, when the thickness is 2.5 mm or less, more preferably 2.0 mm or less,
and still more preferably 1.5 mm or less, a soft artificial leather having excellent
moldability can be obtained.
[0114] In the artificial leather of the present invention, the rubbing fastness measured
by a "9.1 friction tester type I (clock meter) method" according to JIS L 0849: 2013
"Test methods for color fastness to rubbing" and light fastness measured by a "7.2
Exposure method a) First exposure method" according to JIS L 0843: 2006 "Test method
for color fastness to light of xenon arc lamp" are each preferably grade 3 or higher.
When the rubbing fastness and the light fastness are grade 3 or higher, it is possible
to prevent color loss and contamination of clothes and the like during actual use.
[0115] In the artificial leather of the present invention, the mass loss of the artificial
leather after 20,000 times of abrasion under a pressing load of 12.0 kPa in an abrasion
test measured in accordance with "8.19.5 Method E (Martindale method)" of "8.19 Abrasion
strength and color change by rubbing" of JIS L 1096:2010 "Cloth experiment method
of woven fabric and knitted fabric" is preferably 20 mg or less, more preferably 15
mg or less, still more preferably 10 mg or less. When the mass loss is 20 mg or less,
fluff dropping during actual usage can be prevented.
[0116] In the artificial leather of the present invention, the tensile strength as measured
in accordance with "6.3.1 Tensile strength and percentage elongation (ISO method)"
in "Test methods for nonwovens" of JIS L 1913: 2010 is preferably from 20 to 400 N/cm
in arbitrary measurement direction. When the tensile strength is 20 N/cm or more,
more preferably 30 N/cm or more, and still more preferably 40 N/cm or more, the artificial
leather is excellent in shape stability and durability, which is preferable. When
the tensile strength is 400 N/cm or less, more preferably 300 N/cm or less, and still
more preferably 250 N/cm or less, an artificial leather excellent in moldability is
obtained.
[0117] The artificial leather of the present invention preferably has a stiffness of 30
to 150 mm as measured by a cantilever method in "8.21 Stiffness" of JIS L 1096:2010
"Cloth experiment method of woven fabric and knitted fabric", from the viewpoint of
texture and flexibility, and more preferably 50 to 130 mm.
[0118] In the artificial leather of the present invention, the air permeability is preferably
1 to 400 cm
3/cm
2/sec, more preferably 20 to 300 cm
3/cm
2/sec, and still more preferably 70 to 250 cm
3/cm
2/sec in order to achieve both flame retardancy and air permeability in Method A (Frazier
type method) of "8.26 Air permeability" of JIS L 1096: 2010 "Cloth experiment method
of woven fabric and knitted fabric". In the present invention, the air permeability
is greatly affected by the opening; however, when the fiber entanglement has air permeability,
the fiber entanglement is better from the viewpoint of sweatiness and multiplication
of bacteria. Therefore, the air permeability of the fiber entanglement having no opening
portion is preferably 1 to 100 cm
3/cm
2/sec, more preferably 2 to 50 cm
3/cm
2/sec.
[0119] The basis weight of the artificial leather of the present invention is measured according
to "6.2 Mass per Unit Area (ISO method)" in "Test methods for nonwovens" of JIS L
1913: 2010, and is preferably in a range of 50 g/m
2 or more and 800 g/m
2 or less. When the basis weight of the nonwoven fabric is 50 g/m
2 or more, more preferably 100 g/m
2 or more, still more preferably 150 g/m
2 or more, an artificial leather having a sense of fulfillment and an excellent texture
can be obtained. On the other hand, when the basis weight is 800 g/m
2 or less, more preferably 600 g/m
2 or less, and still more preferably 500 g/m
2 or less, a soft artificial leather having excellent moldability can be obtained.
[0120] From the viewpoint of the texture and flexibility of the artificial leather after
formation of the opening, the artificial leather backing material for producing the
artificial leather having the opening portion according to the present invention preferably
has a stiffness of 30 mm or more and 150 mm or less, more preferably 50 mm or more
and 130 mm or less, as measured by the cantilever method in "8.21 Stiffness" of JIS
L 1096: 2010 "Cloth experiment method of woven fabric and knitted fabric". When the
stiffness is 30 mm or more and 150 mm or less, an opening portion is easily formed
in the artificial leather backing material, and for example, when the opening portion
is formed with a hollow punch such as a hole piercing punch, waste of the artificial
leather backing material hollowed out at the opening portion tends to come out from
the hollow portion of the punch, so that productivity of opening forming processing
is improved.
[0121] In the artificial leather backing material of the present invention, the Kinetic
friction coefficient of the functional surface is preferably 0.15 or more and 0.60
or less in terms of the formability of the opening portion and the productivity of
opening forming processing. A friction coefficient affects slipperiness of the functional
agent and an opening device (punch, hollow needle, drill, etc.), for example, in the
case of an opening method is perforation (punch, hollow needle, etc.) and drilling.
[0122] In the artificial leather backing material of the present invention, the adhesion
amount of the functional agent is preferably 2 to 30% by mass with respect to the
artificial leather backing material in terms of the properties of the artificial leather
described above, the formability of the opening, and the productivity of opening forming
processing. When the adhesion amount of the functional agent is less than 2% by mass,
fiber waste hollowed out at the opening portion of the artificial leather backing
material is likely to be loosened, and for example, in the case of a punch, it is
difficult to remove the fiber waste from the hollow portion. When the adhesion amount
of the functional agent is more than 30% by mass, for example, in the case of the
punch, the hollow portion is likely to be clogged with the waste. The adhesion amount
can be calculated from a weight change before and after application similarly to the
adhesion amount, and can also be calculated by chemical analysis such as fluorescent
X-ray.
[Production method for artificial leather]
[0123] The artificial leather of the present invention is preferably produced by applying
a flame retardant having a tackiness of 0.1 N/cm
2 or more and 2.0 N/cm
2 or less to one surface of a napped sheet-shaped article including a fiber entanglement
including ultrafine fibers having an average single fiber diameter of 0.1 um or more
and 10 um or less and an elastomer to form a flame retardant surface, and providing
a plurality of opening portions on at least the flame retardant surface to have. Hereinafter,
the details of each step will be described.
<Step of producing ultrafine fiber-generating fibers>
[0124] The ultrafine fiber constituting the artificial leather of the present invention
can be produced by a conventionally known method, and examples of the method include
a sea-island spinning method, a mixed spinning method, and a split type composite
spinning method in synthetic fiber production. It is preferable to use ultrafine fiber-generating
fibers including two or more kinds of polymer substances having different solubilities
in a solvent in terms of productivity such as formation of the fiber entanglement.
[0125] In an ultrafine fiber generation step, an island portion formed of a resin to be
an ultrafine fiber is formed, and an ultrafine fiber-generating fiber having a sea-island
type composite structure in which an easily soluble polymer forms a sea portion is
produced.
[0126] As the ultrafine fiber-generating fiber, an islands-in-the-sea fiber is used in which
thermoplastic resins having different solvent solubilities are used as a sea portion
(easily soluble polymer) and an island portion (hardly soluble polymer), and the sea
portion is dissolved and removed using a solvent or the like to cause the island portion
to form an ultrafine fiber. Use of the islands-in-the-sea fiber is favorable in view
of the texture or surface quality of the artificial leather, because at the time of
removing the sea portion, a suitable gap can be provided between island portions,
that is, between ultrafine fibers inside a fiber bundle.
[0127] As the method of spinning the ultrafine fiber-generating fiber having a sea-island
composite structure, a method using a mutually arranged polymer body in which a spinneret
for sea-island composite fibers is used and the fiber is spun by mutually arranging
a sea portion and an island portion is preferred from the viewpoint that ultrafine
fibers having a uniform single fiber fineness are obtained.
[0128] As a method of incorporating the pigment into the island portion, even when spinning
is performed using a resin chip obtained by kneading the pigment with the resin of
the island portion, any method can be adopted in which a master batch obtained by
kneading the pigment with the resin is prepared in advance, and the master batch and
chips of another resin are mixed and spun.
[0129] As the sea portion of the islands-in-the-sea fibers, for example, a copolymerized
polyester obtained by copolymerizing polyethylene, polypropylene, polystyrene, sodium
sulfoisophthalic acid, polyethylene glycol or the like, and polylactic acid can be
used, but polystyrene or copolymerized polyester is preferably used from the viewpoint
of yarn making property, easy elutability, and the like.
[0130] In the production method for an artificial leather of the present invention, in the
case of using the islands-in-the-sea fiber, an islands-in-the-sea fiber in which the
strength of the island portion is 2.5 cN/dtex or more is preferably used. When the
strength of the island portion is 2.5 cN/dtex or more, more preferably 2.8 cN/dtex
or more, still more preferably 3.0 cN/dtex or more, the abrasion resistance of the
artificial leather is enhanced, and at the same time, reduction in the rubbing fastness
due to falling off of the fiber can be suppressed.
[0131] In the present invention, the strength of the island portion of the islands-in-the-sea
fibers is calculated by the following method.
- (1) 10 islands-in-the-sea fibers having a length of 20 cm are bundled.
- (2) The sea portion is dissolved and removed from the sample of (1), and an air drying
is performed.
- (3) A test is performed 10 times (N=10) in accordance with "8.5.1 Standard time test"
of "8.5 Tensile strength and percentage elongation" of JIS L 1013:2010 "Testing methods
for man-made filament yarns" under the conditions of a grasp interval of 5 cm, a tensile
speed of 5 cm/min, and a load of 2 N.
- (4) A value obtained by rounding the arithmetic average value (cN/dtex) of the test
results of (3) to the first decimal place is employed as the strength of the island
portion of the islands-in-the-sea fiber.
<Step of producing fiber entanglement>
[0132] A conventional production method for a fiber entanglement in which ultrafine fibers
or islands-in-the-sea fibers are used as a woven/knitted fabric and a nonwoven fabric
can be applied. Preferably, the spun-out ultrafine fiber-generating fiber is opened
and passed through a cross wrapper, etc. to form a fiber web, and the fiber web is
then entangled to obtain a nonwoven fabric. As the method for obtaining the nonwoven
fabric by entangling the fiber web, a needle punching treatment, a water jet punching
treatment, and the like can be used.
[0133] As for the form of the nonwoven fabric, either a short-fiber nonwoven fabric or a
long-fiber nonwoven fabric may be used as described above, and in the case of the
short-fiber nonwoven fabric, the number of fibers oriented in the thickness direction
of the artificial leather is larger than that in the long-fiber nonwoven fabric, and
the surface of the artificial leather at the time of being napped can give a highly
dense feeling.
[0134] In the case where a short-fiber nonwoven fabric is used for the nonwoven fabric,
the obtained ultrafine fiber-generating fibers are preferably crimped, cut to a predetermined
length to obtain a raw cotton, then opened, stacked, and entangled, thereby obtaining
a short-fiber nonwoven fabric. Generally known methods may be used for the crimping
and cutting steps.
[0135] In addition, when the artificial leather includes the woven/knitted fabric (a), the
obtained nonwoven fabric and the woven/knitted fabric (a) are stacked and then integrated
by entanglement. For the entanglement and integration of the nonwoven fabric and the
woven/knitted fabric (a), the woven/knitted fabric (a) is stacked on one surface or
both surfaces of the nonwoven fabric, or the woven/knitted fabric (a) is sandwiched
between a plurality of nonwoven fabric webs, and then the fibers of the nonwoven fabric
and the woven/knitted fabric (a) can be interlaced by needle punching, water jet punching,
or the like.
[0136] The apparent density of the nonwoven fabric including ultrafine fiber-generating
fibers after needle punching or water jet punching is preferably 0.15 g/cm
3 or more and 0.45 g/cm
3 or less. Preferably, when the apparent density is 0.15 g/cm
3 or higher, the sheet-shaped article should have sufficient shape stability and dimension
stability. In addition, preferably, when the apparent density is 0.45 g/cm
3 or lower, a sufficient space can be kept such that the elastomer is imparted.
[0137] It is also preferable for the nonwoven fabric to be subjected to heat shrinkage treatment
with warm water or steam to improve the dense feeling of the fibers.
[0138] Then, the nonwoven fabric may be impregnated with an aqueous solution of a water-soluble
resin and dried to add the water-soluble resin to the nonwoven fabric. Adding the
water-soluble resin to the nonwoven fabric fixes the fibers and improves the dimensional
stability.
<Step of generating ultrafine fiber>
[0139] When the islands-in-the-sea fiber is used, in this step, the obtained fibrous substrate
is treated with a solvent to generate ultrafine fibers having an average single fiber
diameter of single fibers of 0.1 um or more and 10 um or less.
[0140] The development of ultrafine fibers is carried out by immersing the nonwoven fabric
formed of islands-in-the-sea fibers in a solvent to ensure dissolution and removal
of the sea portion of the islands-in-the-sea fibers.
[0141] When the ultrafine fiber-generating fiber is an islands-in-the-sea fiber and the
sea portion is polyethylene, polypropylene or polystyrene, an organic solvent such
as toluene or trichloroethylene can be used as the solvent to dissolve and remove
the sea portion. An aqueous alkali solution of sodium hydroxide or the like can be
used when the sea portion is copolymerized polyester or polylactic acid. Hot water
can be used when the sea portion is water-soluble thermoplastic polyvinyl alcohol-based
resin.
<Step of adding elastomer>
[0142] In this step, a fiber entanglement including ultrafine fibers or ultrafine fiber-generating
fibers as a main component is impregnated with a solution of an elastomer and solidified
to add the elastomer. The method of fixing the elastomer to the fiber entanglement
may be a method of impregnating a solution of the elastomer into the fiber entanglement
and then subjecting the resultant to wet coagulation or dry coagulation, and these
methods can be appropriately selected according to the kind of the used elastomer.
[0143] N,N'-dimethylformamide, dimethyl sulfoxide, or the like is preferably used as the
solvent used when polyurethane is added as the elastomer. A water-dispersible polyurethane
liquid in which polyurethane is dispersed as an emulsion in water may be used.
[0144] The elastomer may be applied to the fiber entanglement before generating ultrafine
fibers from the ultrafine fiber-generating fibers, or after generating ultrafine fibers
from the ultrafine fiber-generating fibers.
<Step of half-cutting and grinding fiber entanglement including elastomer>
[0145] From the viewpoint of production efficiency, it is also a preferable aspect that
after the completion of the step above, the fiber entanglement provided with the elastomer
is cut in half in the thickness direction to form half-cut sheets as two fiber entanglements.
[0146] Furthermore, a napped surface can be formed by applying a napping treatment to the
fiber entanglement provided with the elastomer or a half-cut sheet-shaped article
obtained by cutting in half. The napping treatment can be performed by grinding the
surface using sandpaper or a roll sander. The napping treatment can be applied to
only one surface or both surfaces.
[0147] When the napping treatment is applied, a lubricant such as a silicone emulsion can
be added to the surface of the fiber entanglement before the napping treatment. In
addition, when an antistatic agent is applied before the napping treatment, a ground
powder generated by grinding is less likely to deposit on sandpaper. In this way,
a napped sheet-shaped article having a napped surface is formed.
<Step of dyeing napped sheet-shaped article>
[0148] It is preferable for the napped sheet-shaped article to be dyed. Examples of the
dyeing treatment include jet dyeing treatment using a jigger dyeing machine or a jet
dyeing machine, dip dyeing treatment such as thermosol dyeing treatment using a continuous
dyeing machine, and printing treatment to the napped surface, such as roller printing,
screen printing, inkjet printing, sublimation printing, and vacuum sublimation printing.
In particular, a jet dyeing machine is preferably used from the viewpoint of quality
and appearance from the viewpoint of obtaining a flexible texture. If necessary, the
artificial leather may be subjected to various kinds of resin finishing after the
dyeing.
<Step of stacking and integrating woven/knitted fabric (b)>
[0149] It is preferable that the woven/knitted fabric (b) is stacked and integrated with
an adhesive on a surface opposite to a napped surface (when both surfaces each have
a napped surface, the napped surface on a side to be a product surface) of the napped
sheet. Examples of the method of adding the adhesive include a method of applying
a predetermined amount of the adhesive using a device such as a rotary screen, a knife
roll coater, a gravure roll coater, a kiss roll coater, or a calender coater. In particular,
it is preferable to form a discontinuous adhesive layer using a rotary screen or a
gravure roll coater because the artificial leather has a good texture. Forming a discontinuous
adhesive layer can prevent texture curing and reduction in air permeability of the
artificial leather. The discontinuous adhesive layer means an adhesive layer including
both a portion where an adhesive is present and a portion where an adhesive is absent
with respect to an adhesion surface, that is, a horizontal surface of the woven/knitted
fabric or raised nap sheet. For example, the discontinuous adhesive layer means an
adhesive layer in which the adhesive is arranged in a dot pattern.
[0150] As a bonding method, when a thermoplastic resin is used as an adhesive, the adhesive
can be integrated by thermocompression bonding. For the thermocompression bonding,
a method such as heat rolls can be used. In the case where heat rolls are used, it
is preferable to set the temperature of the heat roll on the woven/knitted fabric
side higher than the temperature of the heat roll on the skin sheet side. When a wet-curable
resin is used as an adhesive, adhesion is promoted under a suitable temperature and
humidity environment called curing.
[0151] The roll temperature on the woven/knitted fabric side in thermocompression bonding
with heat rolls is preferably 80 to 180°C, more preferably 100 to 160°C. If the roll
temperature on the woven/knitted fabric side is lower than 80°C, adhesion takes time,
and a large load is imposed on the process. If the roll temperature on the woven/knitted
fabric side is higher than 180°C, the texture of the artificial leather becomes coarse
and hard.
<Step of adding functional agent (flame retardant or the like)>
[0152] A functional agent (flame retardant or the like) is added to one surface of the napped
sheet-shaped article to form a functional surface (surface of flame retardant or the
like), thereby obtaining an artificial leather backing material. Here, the functional
agent (flame retardant or the like) having a tackiness of 0.1 N/cm
2 or more and 2.0 N/cm
2 or less is applied to obtain the functional surface (surface of flame retardant or
the like). Alternatively, the functional surface has a Kinetic friction coefficient
(JIS K 7125) of 0.15 or more and 0.60 or less, and the artificial leather backing
material has a stiffness of 30 mm or more and 150 mm or less. In this step, the functional
surface (surface of flame retardant or the like) is formed on a surface opposite to
the napped surface (when both surfaces each have a napped surface, the napped surface
on the side to be a product surface) of the napped sheet-shaped article.
[0153] Examples of the method of forming the functional surface (surface of flame retardant
or the like) include a method of applying the functional agent (flame retardant or
the like) to a stacked sheet obtained by stacking the napped sheet-shaped article
or the woven/knitted fabric (b) by using a device such as a rotary screen, a knife
roll coater, a gravure roll coater, a kiss roll coater, or a calender coater. Although
the functional agent (flame retardant or the like) may be applied by a padding treatment
and migrated by drying to be unevenly distributed to a surface layer, stability of
unevenly distributed to the surface layer is poor. The napping treatment may be further
performed after the functional agent (flame retardant or the like) is applied and
dried. Alternatively, the functional agent (flame retardant or the like) may be applied
to the woven/knitted fabric (b) in advance, and then the woven/knitted fabric (b)
may be stacked on the surface opposite to the napped surface (when both surfaces each
have the napped surface, the napped surface on the side to be a product surface) of
the napped sheet-shaped article to form a functional surface (surface of flame retardant
or the like).
[0154] Since the functional agent (flame retardant or the like) permeates the inside after
being applied, the functional agent (flame retardant or the like) is permeated while
adjusting the viscosity of the functional agent (flame retardant or the like), a mesh
of a gravure roll, the application amount, an immersion amount, and the like. As a
drying method after the application of the functional agent (flame retardant or the
like), the drying can be performed using a known dryer such as a tenter dryer.
<Step of forming opening>
[0155] Then, the functional (flame retardant or the like) sheet including the functional
surface (surface of flame retardant or the like) has a plurality of opening portions
at least on the functional surface (surface of flame retardant or the like). Examples
of the means for providing the opening portion include methods such as boring such
as perforation and drilling, and laser processing. The opening portion may be formed
not only on the functional surface (surface of flame retardant or the like) but also
on the other surface. The timing of opening is not limited, and for example, the fiber
entanglement and the woven/knitted fabric (b) may be separately opened and then stacked
and integrated. Preferably, the functional agent (flame retardant or the like) is
applied to the stacked sheet, and a through opening portion is formed by a drill,
a perforated needle, or a hole piercing punch. The artificial leather is obtained
by forming the opening portion.
[0156] Since the artificial leather after the opening portion is formed has a smaller contact
area than before the opening, the Kinetic friction coefficient of the functional surface
decreases. For example, from the viewpoint of stacking a polyurethane foam on the
functional surface by frame lamination or the like, or from the viewpoint of handleability
in the next step, the Kinetic friction coefficient of the functional surface is preferably
0.10 to 0.55 as the artificial leather having the opening portion.
<Post-processing step>
[0157] In addition, in the artificial leather, it is also possible to provide an artificial
leather in which a design may be applied to its surface as necessary. For example,
the surface may be subjected to post processing such as embossing, laser processing,
pinsonic processing, and printing processing.
[0158] The artificial leather of the present invention obtained by the production method
exemplified above is excellent in functionality (flame retardancy and the like) while
having moderate air permeability and a flexible texture, has feels like natural suede
and an elegant appearance, and can be widely used for an interior material for vehicles,
interior materials, building materials, and miscellaneous goods, and in particular,
the artificial leather is suitably used for the interior material for vehicles because
of its excellent functionality (flame retardancy and the like). In addition, the artificial
leather backing material of the present invention obtained by the production method
exemplified above is excellent in opening formability, and is suitably used for the
production of the artificial leather.
EXAMPLES
[0159] Next, the artificial leather of the present invention will be described more specifically
using Examples, but the present invention is not limited only to these Examples. Unless
otherwise described, physical properties are measured based on the methods described
above.
[Measuring methods and processing methods for evaluation]
(1) Average single-fiber diameter of ultrafine fiber (µm)
[0160] In the measurement of the average single fiber diameter of ultrafine fibers, the
average single fiber diameter was calculated by observing the ultrafine fibers by
means of a scanning electron microscope, Model "VW-9000", manufactured by Keyence
Corp.
(2) Abrasion resistance of artificial leather
[0161] After 20,000 times of abrasion under a pressing load of 12.0 kPa in an abrasion test
measured in accordance with "8.19.5 Method E (Martindale method)" of "8.19 Abrasion
strength and color change by rubbing" of JIS L 1096:2010 "Cloth experiment method
of woven fabric and knitted fabric", an abrasion state of the artificial leather surface
was observed and compared with the surface state before the test, and a degree of
abnormality was judged according to the following grade. In this evaluation, grades
3 to 5 were regarded as acceptable.
- Grade 5: not recognized at all.
- Grade 4: slightly recognized; however, hardly conspicuous.
- Grade 3: apparently recognized; however, less conspicuous.
- Grade 2: somewhat remarkable abnormality is recognized.
- Grade 1: considerably remarkable abnormality is recognized.
(3) Tensile strength of artificial leather
[0162] Two specimen sheets of 2 cm × 20 cm were sampled in an arbitrary direction of the
artificial leather, and the tensile strength specified in accordance with "6.3.1 Tensile
strength and percentage elongation (ISO method)" in "Test methods for nonwovens" of
JIS L 1913: 2010 was measured. In the measurement, the average of two sheets was employed
as the tensile strength of the artificial leather.
(4) Appearance quality and feel of artificial leather
[0163] The appearance quality and feel of the artificial leather were evaluated by a total
of 20 evaluators consisting of 10 healthy adult men and 10 healthy adult women and
after visually deciding the following ratings, the most common rating was employed
as the appearance quality and feel of the artificial leather. In the case of a tie
between ratings, a higher rating was employed as the quality and feel of the artificial
leather. The acceptance level of the present invention was "A, B, or C".
- A: Elegant appearance like natural leather, dense surface touch, and premium luxurious
feeling
- B: Although inferior to natural leather, slightly elegant appearance, slightly dense
surface touch, and moderate luxurious feeling
- C: Artificial elegance and surface touch, and low luxurious feeling
- D: Less elegant, rough surface touch, and felt as low-cost product
(5) Evaluation of air permeability of artificial leather
[0164] For each artificial leather to be measured, a 200 mm × 200 mm test piece was taken
from five different positions and subjected to measurement according to Method A (Frazier
type method) of "8.26 Air permeability" of JIS L 1096: 2010 "Cloth experiment method
of woven fabric and knitted fabric", followed by calculating the quantity of air (cm
3/cm
2/sec) passing through the test piece based on the conversion table attached to the
test apparatus. In addition, the five calculations thus obtained were averaged to
give a value to be adopted as the air permeability (cm
3/cm
2/sec).
(6) Test of flexibility of artificial leather
[0165] Based on the cantilever method described in "8.21 Stiffness" of JIS L 1096: 2010
"Cloth experiment method of woven fabric and knitted fabric", the flexibility of the
artificial leather was evaluated by preparing a test piece of 2 cm × 15 cm, placing
the test piece on a horizontal table having a 45° slope, making the test piece to
glide, and reading the scale when a middle point at one end of the test piece was
in contact with the slope.
(7) Flame retardant performance test of artificial leather
[0166] As described above, evaluation was performed based on the burning test standard (horizontal
burning rate) of the automobile interior material of Federal Motor Vehicle Safety
Standards (FMVSS) No. 302. The size of the test piece at this time was 350 mm × 100
mm.
(8) Test of water spot properties of artificial leather
[0167] An artificial leather sample was placed, 3 cm
3 of water was added dropwise onto the surface, the sample was allowed to stand until
it was naturally dried, and then the occurrence of ring stain and the like on the
sample surface was observed. A case where the ring stain and the like were visually
clearly conspicuous was determined to be unacceptable.
(9) Opening ratio of artificial leather
[0168] The opening ratio refers to an area ratio of the opening portion in the entire area
on one surface of the artificial leather, and refers to an area ratio on the surface.
A 20 cm × 20 cm sample of the artificial leather was scanned by image photographing,
an operation of calculating the area ratio by binarization processing was performed
on the sample at 5 points, and the area ratio was determined by arithmetic average.
(10) Presence ratio of flame retardant in thickness direction
[0169] The presence ratio of the flame retardant in the thickness direction was calculated
by the above method after observing the cross section of the artificial leather by
using the scanning electron microscope (SEM), Model "VW-9000", manufactured by Keyence
Corp.
(11) Density of fiber entanglement including elastomer
[0170] The density of the fiber entanglement including the elastomer (the density of the
woven/knitted fabric (b) and the artificial leather containing no flame retardant)
shown in Examples and Comparative Examples was calculated by measuring the basis weight
of the fiber entanglement to which the elastomer was added (including the woven/knitted
fabric (a) when there was the woven/knitted fabric (a)) according to "6.2 Mass per
Unit Area (ISO method)" in "Test methods for nonwovens" of JIS L 1913: 2010 as described
above, and dividing the basis weight by the thickness of the fiber entanglement to
which the elastomer was added. Five samples were randomly taken out from the fiber
entanglement sample including the elastomer, and the average value was taken as the
density.

(12) Tackiness of functional agent
[0171] Measurement and calculation were performed according to the following procedure.
- (1) The functional agent was heated to 60°C.
- (2) Using a tack meter (Tack Taster TA-500 manufactured by Universal Building Materials
Co., Ltd.), a stainless steel probe (contact pressure 24.5 N/cm2) was pressed against the functional agent (flame retardant or the like) at a speed
of 6 mm/min, and held for 5 seconds.
- (3) After (2), a maximum load at the time of peeling at 6 mm/min was read.
- (4) (2) to (3) were repeated five times, and the arithmetic average of the resulting
values was rounded off to the second decimal place to obtain the tackiness at 60°C.
(13) Kinetic friction coefficient
[0172] Three test pieces of 80 mm × 200 mm were taken from the artificial leather, and the
functional surface was measured at a test speed of 100 mm/min, with a sliding piece
of 63 mm × 63 mm, and at a load of 1.92 N according to JIS K 7125, and the average
value was taken as the Kinetic friction coefficient.
[Example 1]
<Step of producing raw stock>
[0173] While polyethylene terephthalate was used as the island component, polystyrene was
used as the sea component, and the island component and the sea component were subjected
to melt spinning using a sea-island composite spinneret having 16 islands under the
conditions of an island/sea mass ratio of 80/20, a discharge rate of 1.2 g/(min-hole),
and a spinning speed of 1,100 m/min, and then 2.7-fold stretching was performed in
a spinning oil solution bath set at 90°C. Then, crimping was performed using a stuffer
box crimper, followed by cutting to a length of 51 mm to provide raw stock of islands-in-the-sea
fiber with a single fiber fineness of 3.8 dtex.
<Step of producing fiber entanglement>
[0174] The raw stock obtained as described above was used to form a laminated web via carding
and cross wrapper steps. The needle punching treatment was performed with a number
of punches of 2,500 punches/cm
2 to obtain a nonwoven fabric having a basis weight of 540 g/m
2 and a thickness of 2.4 mm.
<Step of generating ultrafine fiber>
[0175] The nonwoven fabric obtained as described above was shrunk with hot water at 96°C.
Thereafter, the nonwoven fabric shrunk with hot water was impregnated with a polyvinyl
alcohol (hereinafter, may be abbreviated as PVA) aqueous solution having a saponification
degree of 88%, which was prepared so as to have a concentration of 12% by mass. Furthermore,
the nonwoven fabric was squeezed with rollers and dried by hot air having a temperature
of 120°C for 10 minutes while allowing for migration of PVA, to obtain a PVA-impregnated
sheet in which the mass of PVA was 25% by mass relative to the mass of a sheet base.
The PVA-impregnated sheet thus obtained was immersed in trichloroethylene, and squeezed
and compressed by a mangle ten times. Thus, dissolution removal of the sea portion
and compression treatment of the PVA-impregnated sheet were performed to obtain a
PVA-impregnated sheet in which the ultrafine fiber bundles to which PVA was applied
were entangled. The average single fiber diameter of the ultrafine fiber was 4.4 um.
<Step of adding elastomer>
[0176] A dimethylformamide (hereinafter, may be abbreviated as DMF) solution of polyurethane
prepared so that the concentration of a solid content mainly composed of polyurethane
was 13% was immersed in the PVA-impregnated sheet obtained as described above. Thereafter,
the sea-removing PVA-impregnated sheet immersed in DMF solution of polyurethane was
squeezed with rollers. Then, the sheet was immersed in a DMF aqueous solution having
a concentration of 30% by mass to solidify the polyurethane. After that, PVA and DMF
were removed by hot water, and a silicone oil emulsion solution adjusted to a concentration
of 1% by mass was impregnated, thereby applying a silicone-based lubricant such that
the applied amount thereof was 0.5% by mass relative to the total mass of the mass
of the fiber entanglement and the mass of the polyurethane, and drying was performed
with hot air having a temperature of 110°C for ten minutes. As a result, a polyurethane-impregnated
sheet having a thickness of 1.8 mm and a polyurethane mass of 33% by mass relative
to the mass of the fiber entanglement was obtained. The density of the polyurethane-impregnated
sheet which was the fiber entanglement including the elastomer was 0.35 g/cm
3.
<Step of half-cutting and napping>
[0177] The polyurethane-impregnated sheet obtained as described above was cut in half such
that the thickness of each part was 1/2. Subsequently, a napping treatment was performed
by grinding the surface layer portion of the half-cut surface by 0.3 mm with an endless
sandpaper having a sandpaper grit size of 180 to obtain a napped sheet having a thickness
of 0.6 mm.
<Step of dyeing and finishing>
[0178] The napped sheet obtained as described above was dyed with a black disperse dye at
120°C using a jet dyeing machine, and reduction-cleaned. Thereafter, a drying treatment
was performed at 100°C for 7 minutes to obtain a dyed sheet having an average single
fiber diameter of the ultrafine fiber of 4.4 um, a basis weight of 220 g/m
2, and a thickness of 0.70 mm.
<Flame retardant processing>
[0179] A flame retardant A was obtained by mixing 20 parts by mass of ammonium polyphosphate
treated with a silicon oxide resin (manufactured by Wellchem. com, phosphorus content:
28%, nitrogen content: 14%) as a flame retardant main component of the flame retardant,
0.2 parts by mass of polyoxyethylene sorbitan monostearate (nonionic surfactant) as
a surfactant, 11 parts of methyl acrylate resin having a nonvolatile content of 50%
as a binder resin, and 4 parts by mass of melamine cyanurate (nitrogen content: 49.4%),
and using hydroxyethyl cellulose as a thickener. Coating processing of applying a
flame retardant processing agent solution (the viscosity was adjusted to 3000 mPa-s
by the thickener) containing 70% by mass of the flame retardant A to one surface opposite
to the product surface of the dyed sheet using a screen coater was performed, and
then drying treatment was performed at a temperature of 100°C for 7 minutes to obtain
a sheet with a flame retardant in which the adhesion amount of the flame retardant
with respect to the mass of the artificial leather after drying was 20% by mass.
<Punching>
[0180] In the sheet with a flame retardant, a through opening portion was formed with a
punching board in which needles were planted, thereby obtaining an artificial leather
(needle diameter: 1.2 mm, longitudinal pitch: 5 mm, transverse pitch: 5 mm, opening
ratio: 6%). The through opening portion after the punching was not clogged with fiber
waste, the flame retardant did not stick to an edge of the opening portion, a clean
opening portion was formed, and the fiber waste and the flame retardant did not adhere
to the punching board after the punching in which dust was blown off by air. The obtained
artificial leather had excellent flame retardancy while having moderate air permeability
and a flexible texture, and had dense feels like natural suede and an elegant appearance.
The tackiness of the flame retardant was 0.45 N/cm
2 at 60°C, 0.20 N/cm
2 at 40°C, and 0.14 N/cm
2 at 20°C. The basis weight of the artificial leather was 240 g/m
2, and the thickness was 0.72 mm. The results are shown in Table 1.
[Example 2]
[0181] An artificial leather was obtained in the same manner as in Example 1 except that
an ultrafine fiber-generating fiber having a sea-island composite structure including
an island component and a sea component was subjected to melt spinning using a sea-island
composite spinneret having 16 islands under the conditions of an island/sea mass ratio
of 55/45, a discharge amount of 1.0 g/(min-hole), and a spinning speed of 1100 m/min,
and then the ratio of stretching in a spinning oil solution bath set at 90°C was 3.4
times. The density of the polyurethane-impregnated sheet was 0.360 g/cm
3, which was higher than that in Example 1, and the immersion amount of the flame retardant
was small, so that W/W
0 = 0.07. The average single fiber diameter of the ultrafine fiber was 2.9 um. The
results are shown in Table 1.
[Example 3]
[0182] A laminated web was formed using the raw stock described in Example 1 via the carding
and cross wrapper steps, and then a plain woven fabric (basis weight: 75 g/m
2) having a warp density of 95 yarns/2.54 cm and a weft density of 76 yarns/2.54 cm,
in which a twisted yarn obtained by twisting a multifilament (average single fiber
diameter: 11 um, total fineness: 84 dtex, 72 filaments) containing polyethylene terephthalate
having an intrinsic viscosity (IV value) of 0.65 at 2500 T/m was used for both wefts
and warps, was stacked on and under the laminated web. Thereafter, an artificial leather
in which the average single fiber diameter of the ultrafine fiber was 4.4 um, the
basis weight was 360 g/m
2, and the thickness was 1.0 mm was obtained in the same manner as in Example 1 except
that the needle punching treatment was performed with a number of punches of 2,500
punches/cm
2 to obtain a nonwoven fabric of a fiber entanglement having a basis weight of 700
g/m
2 and a thickness of 3.0 mm. A tough artificial leather having higher strength than
that of Example 1 was obtained. The results are shown in Table 1.
[Example 4]
[0183] A tricot fabric was prepared with a multifilament (total fineness: 48 dtex, 18 filaments)
containing polyethylene terephthalate by using a single tricot machine, and dyed with
a black disperse dye to prepare a dyed tricot fabric having a warp density of 32 yarns/2.54
cm and a weft density of 48 yarns/2.54 cm, and a low-melting-point nylon resin (softening
temperature: 90°C) as an adhesive was applied in an amount of 20 g/m
2 in the form of dots using a gravure roll coater, and then dried with hot air at a
temperature of 100°C to obtain a tricot with an adhesive. The tricot side was thermocompression-bonded
to the dyed sheet of Example 3 with a heat roll heated to a temperature of 150°C to
obtain a composite sheet having a basis weight of 440 g/m
2 and a thickness of 1.1 mm. The composite sheet was subjected to flame retardant processing
and punched in the same manner as in Example 3 to obtain an artificial leather having
a basis weight of 490 g/m
2 and a thickness of 1.2 mm. An artificial leather having higher strength than that
of Example 3 was obtained. The flame retardant adhered to the entire tricot, and the
tricot as a single component had high flame retardancy, so that the artificial leather
had high flame retardancy. The results are shown in Table 1.
[Example 5]
[0184] A circular knitted base fabric was knitted with a blister structure using an interlaced
yarn containing a multifilament (84 dtex/25 f, average single fiber diameter of ultrafine
fibers after sea removal: 9 um) using a sea-island composite yarn using polyethylene
terephthalate as the island component and polystyrene as the sea component and a multifilament
(33 dtex/12 f) of polyethylene terephthalate. An artificial leather including the
fiber entanglement including the elastomer was obtained in the same manner as in Example
1 except that the fiber entanglement was a circular knitted base fabric. The basis
weight of the artificial leather was 240 g/m
2, and the thickness was 0.72 mm. The artificial leather which had a luxurious feeling
in a lower zone as compared with Example 1 and a relatively hard texture, and was
excellent in water spot and punching processability was obtained. The results are
shown in Table 1.
[Example 6]
[0185] An artificial leather having a basis weight of 490 g/m
2 and a thickness of 1.2 mm was obtained in the same manner as in Example 4 except
that with respect to the flame retardant, 30 parts by mass of a dialkylphosphinic
acid metal salt as a main component of the flame retardant and 15 parts by mass of
an acrylic acid ester copolymer as a binder resin were used to obtain a flame retardant
B, and a flame retardant processing agent solution containing 50% by mass of the flame
retardant B was obtained. The tackiness of the flame retardant was 1.50 N/cm
2 at 60°C, 0.50 N/cm
2 at 40°C, and 0.30 N/cm
2 at 20°C. Since the flame retardant had high tackiness at room temperature, the immersion
amount was smaller than that in Example 4, and the tackiness at 60°C was high, an
artificial leather having excellent flame retardancy and appearance quality was obtained
although holes and punching board needles were slightly clogged after punching. The
results are shown in Table 1.
[Example 7]
[0186] An artificial leather was obtained in the same manner as in Example 4 except that
the opening ratio was 14%. Since the number of opening portions was larger than that
in Example 4, the flame retardancy was slightly inferior; however, an artificial leather
excellent in flexibility and the like was obtained. The results are shown in Table
1.
[Comparative Example 1]
[0187] An artificial leather was obtained in the same manner as in Example 4 except that
5 parts by mass of a methyl acrylate resin and 10 parts by mass of an acrylonitrile
resin were used as binder components for the flame retardant. The tackiness was high,
the opening portion was clogged during punching, and the air permeability was poor.
The results are shown in Table 1.
[Comparative Example 2]
[0188] An artificial leather was obtained in the same manner as in Example 4 except that
the average single fiber diameter of the ultrafine fibers was 11 um. A rough surface
touch quality with no elegance was obtained. The results are shown in Table 1.
[Table 1]
|
Example 1 |
Example 2 |
Example 3 |
Example 4 |
Example 5 |
Example 6 |
Example 7 |
Comparative Example 1 |
Comparative Example 2 |
Fiber entanglement |
Average single fiber diameter of ultrafine fiber (µm) |
4.4 |
2.9 |
4.4 |
4.4 |
9.0 |
4.4 |
4.4 |
4.4 |
11.0 |
Fiber entanglement |
Nonwoven fabric |
Nonwoven fabric |
Nonwoven fabric |
Nonwoven fabric |
Knitted fabric |
Nonwoven fabric |
Nonwoven fabric |
Nonwoven fabric |
Nonwoven fabric |
Woven/knitted fabric (a) |
- |
- |
Woven fabric |
Woven fabric |
- |
Woven fabric |
Woven fabric |
Woven fabric |
Woven fabric |
Woven/knitted fabric (b) |
- |
- |
- |
Tricot |
- |
Tricot |
Tricot |
Tricot |
Tricot |
Elastomer |
Polyurethane |
Density of fiber entanglement including elastomer (g/cm3) |
0.35 |
0.36 |
0.40 |
0.40 |
0.30 |
0.40 |
0.40 |
0.40 |
0.42 |
Flame retardant |
Flame retardant main component |
Ammonium polyphosphate |
Dialkylphosp hinic acid metal salt |
Ammonium polyphosphate |
Main resin |
Methyl acrylate |
Acrylic acid ester |
Methyl acrylate |
Acrylonitrile |
Methyl acrylate |
Tackiness at 60° C (N/cm2) |
0.45 |
0.45 |
0.45 |
0.45 |
0.45 |
1.5 |
0.45 |
2.1 |
0.45 |
Artificial leather backing material (before opening) |
Kinetic friction coefficient |
0.29 |
0.28 |
0.31 |
0.27 |
0.29 |
0.41 |
0.25 |
0.61 |
0.31 |
Stiffness (mm) |
70 |
75 |
80 |
95 |
90 |
90 |
90 |
105 |
125 |
Artificial leather |
Thickness (mm) |
0.72 |
0.72 |
1.0 |
1.2 |
0.72 |
1.2 |
1.2 |
1.2 |
0.72 |
Basis weight (g/m2) |
240 |
240 |
360 |
360 |
240 |
360 |
330 |
360 |
362 |
W/W0 |
0.10 |
0.07 |
0.15 |
0.21 |
0.31 |
0.17 |
0.21 |
0.25 |
0.28 |
Opening ratio (%) |
6 |
6 |
6 |
6 |
6 |
6 |
14 |
6 |
6 |
Air permeability (cm3/cm2/sec) |
110 |
105 |
100 |
90 |
110 |
95 |
140 |
65 |
95 |
Flame retardancy (mm/min) |
25 |
30 |
20 |
10 |
40 |
Self-extinguished |
60 |
30 |
7 |
Tensile strength (N/cm) |
50 |
55 |
70 |
80 |
40 |
78 |
70 |
75 |
62 |
Appearance quality and feel |
A |
A |
A |
A |
C |
A |
A |
A |
D |
Abrasion resistance |
5 |
4 |
5 |
5 |
3 |
5 |
4 |
5 |
5 |
Stiffness (mm) |
65 |
70 |
75 |
90 |
85 |
85 |
85 |
100 |
120 |
Water spot |
Acceptable |
Acceptable |
Acceptable |
Acceptable |
Acceptable |
Acceptable |
Acceptable |
Acceptable |
Acceptable |
Punching processability |
Good |
Good |
Good |
Good |
Good |
Slightly good |
Good |
Poor |
Good |
[0189] Particular embodiments have been used to detail the invention. However, it is evident
to those skilled in the art that various alternations and modifications are allowed
without departing from the spirit and scope of the invention.