TECHNICAL FIELD
[0001] This invention relates to a polyamide yarn having on the surface of the polyamide
yarn hydrophobic organic ester dip penetration regulator having a melting point greater
than 27°C and convertible by conventional means into a tire cord having low stiffness
and high air permeability and a process for making polymeric tire yarns.
BACKGROUND
[0002] Fiber finishes having hydrophobic organic ester components, with a melting point
lower than ambient temperature, have been used by fiber producers because of their
ease of handling at ambient temperature. These liquid esters provide lubrication to
the fiber during spinning, plying, twisting, and fabric weaving operations. Unfortunately,
these liquid lubricants tend to promote excessive stiffness in resorcinol-formaldehyde-latex
(RFL) treated cords. This stiffness causes handling problems in tire manufacturing
and it is accompanied by low air permeability of RFL dipped cord which causes excessive
curing blows in tires.
[0003] Triglyceride ester lubricants used in commercial finishes are examples of stiffness-promoting
finish ingredients. Examples of such esters are transesterified triglyceride made
from glyceryl trioleate, coconut oil and palm oil and having a melting point of approximately
21°C and coconut oil with a melting point of approximately 24-27°C.
[0004] It is especially important for tire cords not to have excessive stiffness or poor
air permeability, the cause of which is believed to be excessive dip penetration into
the tire cord. The object of this invention is to develop a tire yarn convertible
to a tire cord, said cord having low stiffness and high air permeability and a process
for making such tire yarn.
[0005] High dipped cord stiffness can be reduced by mechanically exercising fabrics during
the fabric hot stretching process. For example, fabrics can be passed over breaker
or flexing bars under relatively high tensions to physically break apart stuck filaments
to reduce dipped cord stiffness. However , this is undesirable in that some dip is
removed and fabrics may be damaged. Furthermore, mechanical fabric treatments do not
increase dipped cord permeability.
[0006] Fabric hot stretching temperatures and tensions can influence dipped cord air permeability,
but it is difficult to significantly increase air permeability without adversely affecting
other properties such as adhesion. Curing blows caused by low air permeability dipped
cords can be reduced by using lower temperature, longer tire curing cycles, but this
increases tire manufacturing cost.
[0007] Excessive dipped cord stiffness can cause several problems in tire building, including
difficulty in making tight uniform turn-ups and excessive trapped air which aggravates
curing blows in tires. It is physically more difficult to turn carcass fabric plies
around the bead, causing operator discomfort. Even when plies are turned up automatically,
there is a tendency for turn-ups to come loose. Low air permeability leads to excessive
curing blows in tires. Invariably some air is trapped between components as tires
are assembled. If this air collects in pockets during the tire curing process, air
bubbles result in the cured tire, and the tire must be rejected.
SUMMARY OF THE INVENTION
[0008] A polyamide yarn suitable for use as a tire yarn characterized by a tenacity of greater
than 9 g/den., a copper content of greater than 40 parts per million and having on
the surface of the polyamide yarn at least 0.05% based on the weight of the polyamide
yarn hydrophobic organic ester dip penetration regulator, preferably pentaerythritol
tetralaurate or hydrogenated coconut oil, having a melting point greater than 27°C
and convertible by conventional means into a tire cord having an air permeability
as measured by wicking of at least 0.4 liter/30 min., preferably 0.7 liter/30 min.
and preferably a stiffness of less than 40 grams, more preferably less than 30 grams
has been discovered. An ethoxylated nonionic surfactant may preferably be added to
the surface of the polyamide yarn.
[0009] A process for making a tire yarn comprising applying to a synthetic polymeric yarn
at least 0.05% based on the weight of the synthetic polymeric yarn, hydrophobic organic
ester dip penetration regulator, preferably a polyol ester, more preferably a pentaerythritol
ester or a triglyceride, preferably hydrogenated coconut oil, preferably at least
0.25% based on the weight of the synthetic polymeric yarn, having a melting point
greater than 27°C to the synthetic polymeric yarn wherein the tire yarn is convertible
by conventional means into tire cord having low stiffness preferably less than 40
grams and more preferably less than 30 grams and high air permeability preferably
at least 0.4 liter/30 min., more preferably at least 0.7 liter/30 min., has also been
discovered. An ethoxylated nonionic surfactant 0.05-0.5% by weight based on the weight
of the synthetic polymeric yarn is preferably applied to the synthetic polymeric yarn.
An antioxidant 0.001-0.05% by weight based on the weight of the synthetic polymeric
yarn is preferably applied to the synthetic polymeric yarn. The synthetic polymeric
yarn is preferably polyamide yarn, preferably polyhexamethylene adipamide yarn.
[0010] The dip penetration regulator is applied to the synthetic polymeric yarn during yarn
spinning, drawing, winding, or a post-winding operation. It can be applied by itself,
with a diluent, or in combination with a finish. It is conveniently applied by adding
it to a "spin" finish, and applying just after quenching and before the yarn is forwarded
on the feed roll. A suitable "spin" finish typically contains 0-90 wt. % of a hydrophobic
ester lubricant with a melting point below ambient temperatures, 0-95 wt. % of a nonionic
surfactant, 0-5 wt. % of an antioxidant and, optionally, small quantities of other
components. Typical nonionic surfactants include ethoxylated sorbitol and sorbitan
fatty acid esters. When the dip penetration regulator of this invention is applied
together with the "spin" finish, it can be applied as an aqueous emulsion at or above
ambient temperatures, or as a neat oil above ambient temperatures. The dip penetration
regulator can also be conveniently applied to the yarn as an "overlay" finish, after
the yarn has been spun and drawn, immediately before winding. It can also be applied
in a separate operation, after the spinning, drawing and winding operations; for example,
in a rewinding or beaming operation. In the latter methods of application, it is convenient
to apply the dip penetration regulator as a neat oil at temperatures above its melting
point, but it can also be applied in emulsified form.
[0011] Typical synthetic yarns useful for this invention are polyamides, such as 6,6 nylon,
6 nylon and copolymers thereof, polyesters such as polyethylene terephthalate and
copolymers thereof, aramids and polyvinyl alcohol. To meet the strength and durability
requirements for tire applications, the yarns are normally prepared from high viscosity
polymers containing stabilizers and are drawn at high draw ratios to yield high tenacity
yarns. A typical process for preparing polyamide yarns with tenacities greater than
9 gpd, suitable for tire applications, is described in U.S. Patent No. 3,311,691.
[0012] Synthetic polymeric tire yarns are converted to tire cords by a series of steps including:
twisting of the singles yarn; cabling the twisted singles yarn to a tire cord; dipping
the cord in a bath containing the reaction product of resorcinol, formaldehyde and
latex (RFL) at ambient temperatures; and heating and stretching the RFL-containing
cord to produce a strong, stabilized cord ready for rubber embedment. After cabling,
it is common practice to weave the tire cord into fabric and dip and hot-stretch the
fabric so produced. A wide range of cord compositions and structures are possible
through the selection of yarn type and denier, denier per filament, twist level, number
of plies, RFL composition, dip pick up, hot-stretching treating conditions, etc. Polyester
and aramid tire cords or fabrics may require a pre-dip before the RFL dip in order
to achieve acceptable adhesion.
[0013] When the yarns of this invention containing at least 0.05 wt. % dip penetration regulator
based on the weight of yarn are processed into RFL-containing tire cords as described
above, they were found to have surprisingly increased air permeability, as measured
by wicking after rubber embedment, and sharply reduced stiffness. The improvements
are significant with as little as 0.05 wt. % dip penetration regulator on yarn and
are quite dramatic at higher levels of dip penetration regulator, such as 0.1 wt.
% and above. Equally surprising is that the improvements in air permeability and stiffness
are accomplished with little or no loss in the critical property of cord adhesion
to rubber. The dip penetration regulator is believed to function by limiting the RFL
dip penetration, during cord processing, to an area near the surface of the cord.
[0014] Low dipped cord stiffness eliminates problems in making uniform tight turn-ups since
less force is required to bend carcass fabric plies around the bead, and there is
little or no tendency for turn-ups to come loose. This is especially important where
multiple carcass plies are turned up simultaneously. High dipped cord air permeability
allows cords to dissipate trapped air and act as a reservoir, thereby eliminating
curing blows.
TEST METHODS
[0015] For the testing of cord stiffness, cord wicking and cord adhesion, tire yarn samples
were converted into tire cord by the process described in paragraph two for Control
1. The number of plies of yarn per cord varied with yarn denier. For yarns 1070 denier
and above a 2-ply construction was used, wherein the singles yarn twist was 10 'Z'
tpi and the cable twist was 10 'S' tpi. For yarns less than 1070 denier a 3-ply construction
was used, wherein the singles twist was 10 'Z' tpi and the cable twist was 10 'S'
tpi.
Tire Cord Stiffness
[0016] Cord stiffness is a measure of the force, in grams, required to pull a sample of
tire cord through a hole in a Teflon® polytetrafluoroethylene plate. A 2-inch unbent,
unkinked sample of cord was centered and balanced horizontally in the hook on the
end of a vertical wire which was inserted through a circular hole 1.0 cm in diameter
in the center of a horizontal Teflon® plate (90 x 60 x 5 mm). The wire was slowly
raised so that the cord was raised until it contacted the underside of the Teflon®
plate. As the wire continued upward, the cord was bent at about its midpoint and pulled
through the plate. The maximum force required to pull the cord through the plate was
recorded. Ten samples per cord were averaged to give the stiffness in grams.
Wicking of Tire Cords
[0017] The test was conducted as described in ASTM Test D-2692-79 (pages 499-503; 1984 Annual
Book of ASTM Standards, Section 7, Volume 7.01) with the following differences. Nitrogen
was used, rather than air, as the gas which was wicked, and it was determined volumetrically,
using a Precision Wet Test Meter (Precision Scientific Co., Chicago, IL). The molded
sample size was the same as that of Test D-2692-79, but only a single layer of tire
cords was used rather than two layers of fabric. Thus, each sample was comprised of:
2 layers of 6.4 x 89 x 3.2 mm rubber stock, a layer of 38 x 76 x 3.2 mm rubber stock,
a layer of 20 tire cords, a layer of 38 x 76 x 3.2 mm rubber stock and 2 layers of
6.4 x 89 x 3.2 mm rubber stock. The 20 tire cords were laid in (zero tension) parallel
to each other and to the edges of the 38 mm dimensions of the rubber stock; the cords
were evenly spaced over a total distance of 50 mm, centered along the 76 mm dimension.
The rubber stock employed was a combination of natural rubber (80 parts by weight),
styrene-butadiene rubber (20 parts), N351 Black (35 parts), plus minor amounts of
other conventional ingredients. After completing sample preparation in the mold, the
rubber was cured in a press for 40 minutes at 150°C with 20 tons (178 kN) pressure.
The molded sample was then cooled to room temperature and trimmed as in D-2692 to
expose fresh ends of the cord.
[0018] Wicking was determined by clamping the sample between the plates of the test chamber.
After ensuring that there is no leakage around the edges of the sample, one side of
the test chamber was pressured up to 100 psi (690 kPa) with nitrogen gas. Wicking
was the amount of nitrogen in liters that passed along/through the tire cords in 30
minutes as recorded on the West Test Meter. Three molded samples were tested per tire
cord and the results averaged. The wicking so determined is considered to be predictive
of the air permeability of the tire cord in a tire.
Hot, Two-Ply Strip Adhesion Test
[0019] The test utilized was the same as ASTM Test D-4393-85, Strap Peel Adhesion of Reinforcing
Cords or Fabrics to Rubber Compounds (pages 1133-1142; 1985 Annual Book of ASTM Standards,
Section 7, Volume 7.01) with a few modifications. The particular variation used was
to test individual tire cords, 1260 denier/2 ply, that had been RFL dipped singly.
The rubber stock was the same formulation of natural rubber and styrene/butadiene
rubber described under the Wicking Test Method. The 1260/1/2 tire cords were warped
at 36 ends/inch (vs. 24 in D-4393-85). After embedment of the cords in the rubber
stock, the sample was cured at 160°C +/- 2°C for 20 minutes at 62kN pressure. Since
hot adhesion was desired, the samples were heated in the Instron oven at 120°C +/-
2°C for 25 +/- 5 minutes prior to testing. The separation force was based on Option
1 or the mid-line between the high and low peaks of separation force. Four samples
per warp were tested and the results were reported as average force in pounds per
inch.
EXAMPLES
CONTROL 1
[0020] Freshly spun filament yarn of polyhexamethylene adipamide of 70 relative viscosity
as measured in United States Patent 2,385,890 and containing 64 parts per million
copper as a stabilizer in the form of a cupric salt was two-stage drawn (5.2x), annealed
(220°C), relaxed (5-6%) and wound according to the process described in United States
Patent 3,311,691. Finish (1.2 weight percent based based on weight of yarn) was applied
to the yarn as a neat oil at about 75°C via a kiss roll applicator located at the
bottom of the spinning chimney, just before the feed roll; this is usually referred
to as the "spin" finish. The "spin" finish was a mixture of four ingredients: 29 weight
percent of a nonionic surfactant, a polyethoxylated oleate of sorbitan; 3 weight percent
of a hindered phenolic antioxidant; 1 weight percent of a substituted polysiloxane;
and 67 weight percent of hydrophobic organic ester lubricant, which is an unsaturated
triglyceride derived from glyceryl trioleate, coconut oil and palm oil (melting point
21°C). The tire yarn so produced was 1260 denier and contained 210 filaments. It had
a typical tire yarn tenacity of 9.8 g/den. as measured with 3 tpi yarn twist.
[0021] The above tire yarn was converted into a conventional 2-ply 1260/1/2 tire cord (singles
twist = 10 'Z' tpi; cable twist = 10 'S' tpi) and processed on a multi-end, 3-oven
hot stretching unit using the following process parameters in ovens 1/2/3: temperature
= 138°C/room temperature/238°C; exposure time = 108/54/54 seconds; applied stretch
= 2.4/2.4/0.0%. Cords were passed through a resorcinol-formaldehyde-latex (D5A) dip
(20% dip solids) before entering the first oven.
[0022] The dipped and stretched cord so prepared was characterized in terms of dip-pick-up
(DPU), stiffness, wicking, and hot two-ply adhesion. See Table I for the data. Although
an excellent tire cord in most respects, the cord was undesirably stiff (41 g.) and
showed a low level of wicking (.08 liters/30 min.).
EXAMPLE 1
[0023] This Example describes the preparation of polyhexamethylene adipamide tire cords
which showed substantial advantages over Control 1 in terms of stiffness and wicking
via "spin" finish modification.
[0024] Five different Samples, A-E, of polyhexamethylene adipamide tire yarns were prepared
in the same manner as Control 1 above, except for the following differences in the
spin finish: higher melting hydrophobic organic esters were substituted in place of
the unsaturated triglyceride in all of the Samples (see Table II) and a mixture of
polyethoxylated sorbitol fatty acid esters was used in Sample C as the nonionic surfactant
in place of the polyethoxylated oleate of sorbitan. Two of the higher melting esters,
hydrogenated coconut oil (mp 39°C; Samples A-C) and pentaerythritol tetralaurate (mp
34°C; Samples D-E), exemplify the kind of dip penetration regulators characteristic
of this invention. Lower melting point coconut oil (mp 24-27°C) when used as the sole
spin finish lubricant, without added dip penetration regulator does not produce the
desirable results of this invention (see Control 2). Compositions of the finishes
applied to the Sample yarns and to Control 1 yarn are given in Table II.
[0025] Sample tire yarnds A-E were converted to tire cords in the same way as for Control
1; tire cord properties are given in Table I. From Table I, it can be seen that the
relatively simple change in finish composition of the tire yarn to include at least
a portion of hydrophobic organic ester dip penetration regulator with mp greater than
27°C yielded rather dramatic changes in tire cord stiffness and wicking. Thus, the
tire cord stiffness of Samples A-E ranged from 39 to 71% lower than that of Control
1, while wicking was 12.5 to 40 times greater than Control 1. Hot two-ply adhesion
values for Samples A-E were about the same as that of Control 1.
EXAMPLE 2
[0026] This Example describes the preparation of polyhexamethylene adipamide tire cords
with improved stiffness and wicking through the use of special "overlay" finishes.
[0027] Control 1 polyhexamethylene adipamide tire yarn, prepared as described above and
containing 1.2% of the Control 1 "spin" finish given in Table II, was modified by
applying the higher melting dip penetration regulators as "overlay" finishes in an
off line process to the drawn, annealed and relaxed yarn. The higher melting dip penetration
regulators used were hydrogenated coconut oil (mp 39°C), Sample F, and pentaerythritol
tetralaurate (mp 34°C), Sample G. Application of the "overlay" finish was effected
by running Control 1 yarn through a slotted applicator to which the dip pentration
regulator was metered as a neat oil at a temperature of about 70°C. The conditions
were adjusted such that Sample F picked up 0.6 wt. % of hydrogenated coconut oil,
while Sample G picked up 0.5 wt. % of pentaerythritol tetralaurate based on the weight
of the yarn.
[0028] The tire yarns prepared as above were converted to tire cords in the same manner
as Control 1 yarn. Cord properties are listed in Table I. Opposite Control 1, it can
be seen that Samples F and G showed a marked decrease in cord stiffness of 46% and
a dramatic increase in wicking of 9-24 fold.
EXAMPLE 3 AND CONTROL 2
[0029] Example 3 shows the beneficial effects of a very low level of a high melting dip
penetration regulator on the stiffness and wicking of polyhexamethylene adipamide
tire cord.
[0030] A polyhexamethylene adipamide tire yarn was prepared in the same way as Control 1,
except that the "spin" finish was changed to the following composition: coconut oil
(82 wt. %; mp = 24-27°C), hindered phenolic antioxidant (3 wt. %), and sorbitan tristearate-20
ethylene oxide (15 wt. %); this yarn was Control 2. Another yarn was prepared in the
same manner and with the same "spin" finish as Control 2, except that the coconut
oil level in the finish was reduced to 77 wt. % and 5 wt. % of hydrogenated palm oil
(mp 61°C) was added; this yarn was Example 3. Example 3 and Control 2 were converted
to tire cords and hot-stretched by procedures similar to those used for Control 1.
Test results on the cords are given in Table III. It can be seen that, even with as
little as 5 weight percent based on the weight of finish of a higher melting dip penetration
regulator in the "spin" finish, such as hydrogenated palm oil, tire cord stiffness
was reduced by 12%, wicking was noticeably increased and adhesion was not adversely
affected.

1. A process for making tire yarn comprising applying to a synthetic polymeric yarn
at least 0.05%, based on the weight of the synthetic polymeric yarn, hydrophobic organic
ester dip penetration regulator, having a melting point greater than 27°C to the synthetic
polymeric yarn wherein the tire yarn is convertible by conventional means into tire
cord having low stiffness and high air permeability.
2. The process of Claim 1 wherein the regulator is a polyol ester.
3. The process of Claim 2 wherein the polyol ester is a pentaerythritol ester.
4. The process of Claim 2 wherein the polyol ester is a triglyceride.
5. The process of Claim 4 wherein the triglyceride is hydrogenated coconut oil.
6. The process of any one of Claims 1 to 5 or 7 further comprising applying 0.05-0.5%
ethoxylated nonionic surfactant by weight based on the weight of the synthetic polymeric
yarn.
7. The process of Claim 5 wherein at least 0.25% hydrogenated coconut oil by weight
based on the weight of the synthetic polymeric yarn is applied.
8. The process of any one of Claims 1 to 7 further comprising applying 0.001-0.05%
antioxidant compound by weight based on the weight of the synthetic polymeric yarn.
9. The process of any one of Claims 1 to 8 wherein the synthetic polymeric yarn is
polyamide yarn.
10. The process of Claim 9 wherein the polyamide yarn is polyhexamethylene adipamide
yarn.
11. The process of any one of Claims 1 to 10 wherein the air permeability as measured
by wicking of the tire cord is at least 0.40 liters/30 min.
12. The process of any one of Claims 1 to 11 wherein the stiffness of the tire cord
is less than 40 grams.
13. The process of Claim 11 or Claim 12 wherein the air permeability as measured by
wicking of the tire cord is at least 0.7 liter/30 min.
14. The process of Claim 12 or Claim 13 wherein the stiffness of the tire cord is
less than 30 grams.
15. A polyamide yarn suitable for use as a tire yarn characterized by a tenacity of
greater than 9 g/den., a copper content of greater than 40 parts per million and having
on the surface of the polyamide yarn at least 0.05% based on the weight of the polyamide
yarn hydrophobic organic ester dip penetration regulator having a melting point greater
than 27°C and convertible by conventional means into a tire cord having an air permeability
as measured by wicking of at least 0.4 liters/30 min.
16. The polyamide yarn of Claim 15 further characterized by the tire cord having a
stiffness of less than 40 grams.
17. The polyamide yarn of Claim 15 or Claim 16 wherein the regulator is pentaerythritol
tetralaurate.
18. The polyamide yarn of Claim 15 or Claim 16 wherein the regulator is hydrogenated
coconut oil.
19. The polyamide yarn of any one of Claims 15 to 18 further characterized by having
on the surface of the polyamide yarn 0.05-0.5% ethoxylated nonionic surfactant by
weight based on the weight of the polyamide yarn.
20. The polyamide yarn of any one of Claims 15 to 19 wherein the air permeability
is greater than 0.7 liter/30 min. and the stiffness is less than 30 grams.
21. The polyamide yarn of any one of Claims 15 to 20 wherein the polyamide yarn is
polyhexamethylene adipamide yarn.