[Technical Field]
[0001] The present invention relates to a polyethylene yarn, a method for manufacturing
the same, and a skin cooling fabric including the same. More particularly, the present
invention relates to a polyethylene yarn which enables the manufacture of a skin cooling
fabric having a dimensional stability and having improved weavability which can provide
a user with a soft tactile sensation as well as a cooling feeling or a cooling sensation,
a method for manufacturing the same, and a skin cooling fabric including the same.
[Background Art]
[0002] As global warming progresses, there is an increasing need for fabrics that can be
used to overcome intense heat. Factors that can be considered in developing fabrics
that can be used to overcome the intense heat include (i) removal of factors that
cause intense heat and (ii) removal of heat from the user's skin.
[0003] A method focused on the removal of factors of intense heat, a method of reflecting
light by applying an inorganic compound to the surface of the fiber (for example,
see
JP 4227837B), a method of scattering light by dispersing inorganic fine particles inside and
on the surface of the fiber (for example, see
JP 2004-292982A) and the like have been proposed. However, blocking these external factors can only
prevent additional intense heat, and for users who already feel heat, there is a limit
that not only can it not be a significant solution, but also the tactile sensation
of the fabric is degraded.
[0004] On the other hand, as a method capable of removing heat from a user's skin, a method
of improving moisture absorption of the fabric in order to utilize the heat of evaporation
of sweat (for example, see
JP 2002-266206A), a method of increasing a contact area between the skin and the fabric in order
to increase the heat transfer from the skin to the fabric (for example, see
JP 2009-24272A), and the like have been proposed.
[0005] However, in the case of using the evaporation heat of sweat, since the function of
the fabric depends greatly on external factors such as humidity or the user's constitution,
there is a problem that its consistency cannot be guaranteed. In the case of a method
of increasing the contact area between the skin and the fabric, as the contact area
increases, the air permeability of the fabric decreases, so that many cooling effects
that the user wants cannot be obtained.
[0006] Thus, it may be desirable to increase heat transfer from the skin to the fabric by
improving the thermal conductivity of the fabric itself. To achieve this purpose,
JP 2010-236130A proposes manufacturing fabrics using ultra-high strength polyethylene fibers (Dyneema
® SK60) having high thermal conductivity.
[0007] However, Dyneema
® SK60 fiber used in
JP 2010-236130A is an Ultra High Molecular Weight Polyethylene (UHMWPE) fiber having a weight average
molecular weight of 600,000 g/mol or more. Even if it exhibits high thermal conductivity,
since it can be produced only by a gel spinning method due to the high melt viscosity
of UHMWPE, there is a problem that environmental problems are caused and considerable
costs are required to recover the organic solvent. Further, since Dyneema
® SK60 fiber has high strength of 28 g/d or more, a high tensile modulus of 759 g/d
or more, and a low elongation at break of 3 to 4 %, the weavability is not good. In
addition, since Dyneema
® SK60 fiber has excessively high stiffness, it is unsuitable for use in the manufacture
of skin cooling fabrics that are intended for contacting with the user's skin.
[0008] Even if yarns for skin cooling fabrics are made of polyethylene having a relatively
lower weight average molecular weight than that of UHMWPE, excessively high shrinkage
stress, dry thermal shrinkage, and wet thermal shrinkage at high temperatures may
result in deformation of the fabric during the dyeing and heat setting processes of
the fabric and during the washing of the final product.
[DETAILED DESCRIPTION OF THE PRESENT DISCLOSURE]
[Technical Problem]
[0009] Therefore, the present invention is directed to providing a polyethylene yarn that
can prevent one or more of the problems due to limitations and disadvantages of the
related arts, a method for manufacturing the same, and a skin cooling fabric including
the same.
[0010] An aspect of the present invention is to provide a polyethylene yarn capable of providing
a user with a soft tactile sensation as well as a cooling feeling or a cooling sensation,
and also having improved weavability that enables the manufacture of a skin cooling
fabrics having excellent dimensional stability.
[0011] Another aspect of the present invention is to provide a method for manufacturing
a polyethylene yarn capable of providing a user with a soft tactile sensation as well
as a cooling feeling or a cooling sensation, and also having improved weavability
that enables the manufacture of a skin cooling fabrics having excellent dimensional
stability.
[0012] Yet another aspect of the present invention is to provide a fabric capable of providing
a user with a soft tactile sensation as well as a cooling feeling or a cooling sensation,
and also having excellent dimensional stability.
[0013] Additional advantages, objects, and features of the invention will be set forth in
part in the description which follows and in part will become apparent to those having
ordinary skill in the art upon examination of the following or may be learned from
practice of the invention.
[Technical Solution]
[0014] In accordance with one aspect of the present invention as described above, a polyethylene
yarn is provided, wherein,
- (i) in a graph showing a shrinkage stress due to the temperature rise, obtained under
the conditions of an initial load of 0.1 g/d and a temperature rising rate of 2.5
°C/s, a shrinkage stress at 70 °C, and the shrinkage stress at 100 °C were 0.005 to
0.075 g/d, respectively,
- (ii) a dry thermal shrinkage rate after being placed in air at 70 °C for 15 minutes
under a load of 0.1 g/d is 0.1 to 0.5 %,
- (iii) a dry thermal shrinkage rate after being placed in air at 100 °C for 15 minutes
under a load of 0.1 g/d is 0.5 to 1.5 %, and
- (iv) a wet thermal shrinkage rate after being immersed in hot water at 100 °C for
30 minutes is 0.1 to 1 %.
[0015] The polyethylene yarn may have an interlacing number of 10 to 40 ea/m.
[0016] Oil pick-up (OPU) of the polyethylene yarn may be 1 to 4 wt%.
[0017] The polyethylene yarn may be a twisted yarn having a twist number of 50 to 300 TPM
(twists per meter) in the Z direction.
[0018] The polyethylene yarn may have tensile strength of more than 4 g/d and 6 g/d or less,
a tensile modulus of 15 to 80 g/d, elongation at break of 14 to 55 %, and crystallinity
of 60 to 85 %.
[0019] The polyethylene yarn may have a weight average molecular weight (Mw) of 50,000 to
99,000 g/mol.
[0020] The polyethylene yarn may have total fineness of 75 to 450 denier, and the polyethylene
yarn may include a plurality of filaments each having a DPF (denier per filament)
of 1 to 5 denier.
[0021] The polyethylene yarn may have a circular cross-section.
[0022] In accordance with another aspect of the present invention, a skin cooling fabric
including the polyethylene yarns as a weft yarn and a warp yarn is provided, wherein
- (i) dry thermal shrinkage rates in the directions of warp and weft after heat treatment
in a chamber at 70 °C for 15 minutes are 0.1 to 1.0 %, respectively,
- (ii) dry thermal shrinkage rates in the directions of warp and weft after heat treatment
in a chamber at 100 °C for 15 minutes are 0.3 to 1.2 %, respectively, and
- (iii) wet thermal shrinkage rates in the directions of warp and weft after immersion
in hot water at 100 °C for 30 minutes are 0.2 to 1.0 %, respectively.
[0023] The dry thermal shrinkage rate and the wet thermal shrinkage rate are measured according
to the ASTM D 1776 method.
[0024] The skin cooling fabric at 20 °C may have a thickness direction thermal conductivity
of 0.0001 W/cm· °C, a thickness direction heat transfer coefficient of 0.001 W/cm
2· °C, and a contact cold sensation (Q
max) of 0.1 W/cm
2 or more.
[0025] The area density of the skin cooling fabric may be 75 to 800 g/m
2.
[0026] In accordance with another aspect of the present invention, a method for manufacturing
a polyethylene yarn is provided, including the steps of:
melting a polyethylene having a density of 0.941 to 0.965 g/cm3, a weight average molecular weight (Mw) of 50,000 to 99,000 g/mol, and a melt index
(MI) (at 190 °C) of 6 to 21 g/10 min,
extruding the molten polyethylene through a spinneret having a plurality of spinning
holes;
cooling a plurality of filaments formed when the molten polyethylene is discharged
from the holes of the spinneret;
drawing a multifilament composed of the cooled filaments using a multistage drawing
part including a series of godet rollers; and
winding the drawn multifilament with a winder,
wherein an overfeed ratio defined by Equation 1 below is 6 to 10 %.

[0027] In Equation 1, OFR is the overfeed ratio, V
1 is the speed of the last godet roller of the multistage drawing part, and V
2 is the speed of the winder.
[0028] The general description related to the present invention given above is intended
only to illustrate or disclose the present invention and should not be construed as
limiting the scope of the present invention.
[ADVANTAGEOUS EFFECTS]
[0029] The polyethylene yarn for a skin cooling fabric of the present invention has high
thermal conductivity, shrinkage properties adjusted to an appropriate range, and excellent
weavability, and can be easily manufactured at a relatively low cost without causing
environmental problems.
[0030] In addition, the skin cooling fabric woven from the polyethylene yarn of the present
invention (i) can consistently provide a user with a cooling sensation regardless
of external factors such as humidity, (ii) can continuously provide a user with a
sufficient cooling sensation without sacrificing air permeability, (iii) can provide
a soft tactile sensation to a user, and (iv) does not cause deformation due to post-processing
such as dyeing, heat setting, etc., as well as washing of the final product.
[BRIEF DESCRIPTION OF DRAWINGS]
[0031] The accompanying drawings, which are included to provide further understanding of
the invention and are incorporated in and constitute a part of this application, illustrate
embodiment(s) of the invention, and together with the description serve to explain
the principle of the invention.
FIG. 1 schematically shows an apparatus for manufacturing a polyethylene yarn according
to an embodiment of the present invention.
FIG. 2 schematically shows an apparatus for measuring the contact cold sensation (Qmax) of a skin cooling fabric.
FIG. 3 schematically shows an apparatus for measuring the thermal conductivity and
heat transfer coefficient in the thickness direction of the skin cooling fabric.
[DETAILED DESCRIPTION OF THE EMBODIMENTS]
[0032] Hereinafter, embodiments according to the present invention will be described in
detail with reference to the accompanying figures. However, the embodiments described
below are provided for illustrative purposes only to help clear understanding of the
present invention and should not be construed as limiting the scope of the present
invention.
[0033] In order to make the user feel a sufficient cooling sensation, the yarns used in
the manufacture of the skin cooling fabric are preferably polymer yarns having high
thermal conductivity.
[0034] In the case of a solid, heat is generally transferred through the movement of free
electrons and lattice vibrations called "phonon". In the case of a metal, heat is
transferred in the solid mainly by the movement of free electrons. In contrast, in
the case of nonmetallic materials such as polymers, heat is mainly transferred through
the phonon within the solid (especially in the direction of the molecular chains connected
via covalent bonds).
[0035] In order to improve the thermal conductivity of the fabric so that the user can feel
a cooling sensation, it is necessary to enhance the heat transfer capability through
the phonon of the polymer yarn by increasing the crystallinity of the polymer yarn
to 60 % or more.
[0036] According to the present invention, in order to produce a polymer yarn having such
high crystallinity, high density polyethylene (HDPE) is used. This is because yarns
made from high density polyethylene (HDPE) having a density of 0.941 to 0.965 g/cm
3 have relatively high crystallinity as compared with yarns made from low density polyethylene
(LDPE) having a density of 0.910 to 0.925 g/cm
3 and yarns made from linear low density polyethylene (LLDPE) having a density of 0.915
to 0.930 g/cm
3.
[0037] Meanwhile, the high density polyethylene (HDPE) yarn may be classified into an ultra
high molecular weight polyethylene (UHMWPE) yarn and a high molecular weight polyethylene
(HMWPE) yarn according to their weight average molecular weight (Mw). The UHMWPE generally
refers to a linear polyethylene having a weight average molecular weight (Mw) of 600,000
g/mol or more, whereas the HMWPE generally refers to a linear polyethylene having
a weight average molecular weight (Mw) of 20,000 to 250,000 g/mol.
[0038] As mentioned above, since UHMWPE yarns such as Dyneema
® can only be produced by gel spinning due to the high melt viscosity of UHMWPE, there
is a problem that environmental problems are caused and considerable costs are required
to recover the organic solvent.
[0039] Since HMWPE has a relatively low melt viscosity compared to UHMWPE, melt spinning
is possible, and as a result, environmental and high cost problems associated with
UHMWPE yarns can be overcome. Therefore, the polyethylene yarn for a skin cooling
fabric of the present invention is a yarn formed of HMWPE.
[0040] The polyethylene yarn of the present invention has the following shrinkage properties:
- (i) in a graph showing a shrinkage stress due to a temperature rise, obtained under
the conditions of an initial load of 0.1 g/d and a temperature rising rate of 2.5
°C/s, the shrinkage stress at 70 °C and the shrinkage stress at 100 °C were 0.005
to 0.075 g/d, respectively;
- (ii) the dry thermal shrinkage rate after being placed in air at 70 °C for 15 minutes
under a load of 0.1 g/d is 0.1 to 0.5 %;
- (iii) the dry thermal shrinkage rate after being placed in air at 100 °C for 15 minutes
under a load of 0.1 g/d is 0.5 to 1.5 %; and
- (iv) the wet thermal shrinkage rate after being immersed in hot water at 100 °C for
30 minutes is 0.1 to 1 %.
[0041] If the shrinkage stress at 70 °C and the shrinkage stress at 100 °C of the polyethylene
yarn is too small, the crystallinity and orientation of the yarn are reduced due to
the low draw ratio in the drawing step, and thus, the fabric made from the yarn does
not have a sufficient cooling sensation. Therefore, the shrinkage stress at 70 °C
and the shrinkage stress at 100 °C of the polyethylene yarn are preferably 0.005 g/d
or more, respectively.
[0042] However, if the shrinkage stress at 70 °C and the shrinkage stress at 100 °C is too
large, the yarn has excessively high strength due to the high draw ratio in the drawing
step, and thus, the weavability is lowered and the cuttability of the final fabric
is also lowered. Therefore, the shrinkage stress at 70 °C and the shrinkage stress
at 100 °C of the polyethylene yarn are preferably 0.075 g/d or less, respectively.
[0043] Specifically, the polyethylene yarn has shrinkage stress at 70 °C of 0.005 to 0.075
g/d, 0.005 to 0.050 g/d, 0.007 to 0.025 g/d, or 0.007 to 0.015 g/d. The polyethylene
yarn has a shrinkage stress at 100 °C of 0.005 to 0.075 g/d, 0.015 to 0.060 g/d, 0.025
to 0.050 g/d, or 0.030 to 0.045 g/d.
[0044] If the dry thermal shrinkage rate at 70 °C of the polyethylene yarn is too low, the
shrinkage due to heat is too small, and in the case of a fabric woven with this yarn,
the spacing between the warp and weft intersections (i.e., voids) becomes excessively
large, allowing air to easily pass through, which reduces the cooling sensation of
the fabric. Therefore, the dry thermal shrinkage rate at 70 °C of the polyethylene
yarn is preferably 0.1 % or more.
[0045] However, if the dry thermal shrinkage rate at 70 °C is too high, excessive shrinkage
due to heat occurs in the heat treatment step or the heat treatment step after dyeing
in the fabric manufacturing process, the fabric becomes stiffer, and the tactile sensation
of the final fabric is reduced. Therefore, the dry thermal shrinkage rate at 70 °C
of the polyethylene yarn is preferably 0.5 % or less.
[0046] Specifically, the polyethylene yarn may have a dry thermal shrinkage rate at 70 °C
of 0.10 to 0.50 %, 0.20 to 0.50 %, 0.20 to 0.40 %, or 0.20 to 0.35 %.
[0047] As the dry thermal shrinkage rate at 100 °C of the polyethylene yarn is lower, it
is more advantageous in terms of dimensional stability. However, shrinkage due to
heat is insufficient, and thus the tensile strength and tear strength of the final
fabric become insufficient, such that a phenomenon in which the fabric is easily torn
occurs. Therefore, the dry thermal shrinkage rate at 100 °C of the polyethylene yarn
is preferably 0.5 % or more.
[0048] However, if the dry thermal shrinkage rate at 100 °C is too high, excessive shrinkage
due to heat occurs during the heat treatment step or the post-dyeing heat treatment
step in the fabric manufacturing process, the fabric becomes stiffer, and the tactile
sensation of the final fabric is reduced. In addition, it is difficult to accurately
match the final fabric density and the fabric width to be designed. Therefore, the
dry thermal shrinkage rate at 100 °C of the polyethylene yarn is preferably 1.5 %
or less.
[0049] Specifically, the polyethylene yarn may have a dry thermal shrinkage rate at 100
°C of 0.50 to 1.50 %, 0.75 to 1.50 %, 0.75 to 1.25 %, or 0.80 to 1.00 %.
[0050] As the wet thermal shrinkage rate at 100 °C of the polyethylene yarn is lower, it
is more advantageous in terms of dimensional stability. However, shrinkage due to
heat is insufficient, and thus the tensile strength and tear strength of the final
fabric become insufficient, such that a phenomenon in which the fabric is easily torn
occurs. Therefore, the wet thermal shrinkage rate at 100 °C of the polyethylene yarn
is preferably 0.1 % or more.
[0051] However, if the wet thermal shrinkage rate at 100 °C is too high, not only is the
fabric size reduced or the fabric becomes stiffer due to excessive shrinkage of the
yarn when performing the post-dyeing heat treatment step, but also the fabric is deformed
when end consumers wash the fabric. Therefore, the wet thermal shrinkage rate at 100
°C of the polyethylene yarn is preferably 1 % or less.
[0052] Specifically, the polyethylene yarn may have a wet thermal shrinkage rate at 100
°C of 0.10 to 1.00 %, 0.50 to 1.00 %, 0.50 to 0.90 %, or 0.70 to 0.85 %.
[0053] According to one embodiment of the invention, the polyethylene yarn may have an interlacing
number of 10 to 40 ea/m.
[0054] The interlacing is performed to strengthen the convergence between filaments forming
the yarn. The better the convergence between filaments, the higher the weavability
of the yarn. However, in the case of conventional polyethylene yarns having relatively
high strength and relatively low elongation, the interlacing number was at the level
of 3 to 5 ea/m because of the high risk of causing pills or yarn breakage in the interlacing
process.
[0055] In contrast, since the polyethylene yarn of the present invention has relatively
low strength and relatively high elongation, a high level of interlacing (i.e., 10
ea/m or more) can be imparted without causing pills or yarn breakage. However, even
in the case of polyethylene yarn of the present invention, if the interlacing number
exceeds 40 ea/m, there is a risk of causing pills or yarn breakage.
[0056] In the case of conventional polyethylene yarn, it was necessary to additionally perform
a twisting step in order to satisfy the required convergency in spite of the low interlacing
number of 5 ea/m or less. On the contrary, the polyethylene yarn according to one
embodiment of the present invention can satisfy the required convergence even without
a separate twisting step, because of the high interlacing number of 10 ea/m or more,
and thus the productivity of the yarn can be improved.
[0057] However, the polyethylene yarn of the present invention is not limited to untwisted
yarn, and in order to further improve the convergence of the filaments, it may be
a twisted yarn. For example, the polyethylene yarn of the present invention may be
a twisted yarn having a twist number of 50 to 300 TPM (twists per meter) in the Z
direction. If the twist number is less than 50 TPM, a satisfactory convergence strengthening
effect cannot be achieved. On the other hand, if the twist number exceeds 300 TPM,
not only does the final fabric become stiffer but also the smoothness of the fabric
surface is degraded, which is disadvantageous in terms of cooling sensation.
[0058] According to one embodiment of the present invention, the oil pick-up (OPU) of the
polyethylene yarn may be 1 to 4 wt%.
[0059] The emulsion attached to the filaments forming the yarn is to improve the weavability
of the yarn. If the OPU is less than 1 wt%, continuous weaving is impossible due to
generation of pills or yarn breakage in the weaving step. On the other hand, when
the OPU exceeds 4 wt%, an excessive amount of emulsion causes oil to adhere continuously
to the loom body when weaving the fabric with the yarn, causing problems in weavability.
In the refining and dyeing step, the emulsion is not properly removed, or there is
a burden of having to perform many washing steps for complete removal.
[0060] The polyethylene yarn according an embodiment of the present invention has tensile
strength of 4 g/d or more and 6 g/d or less, a tensile modulus of 15 to 80 g/d, elongation
at break of 14 to 55 %, and crystallinity of 60 to 85 %. Preferably, the polyethylene
yarn has tensile strength of 4.5 g/d to 5.5 g/d, a tensile modulus of 40 to 60 g/d,
elongation at break of 20 to 35 %, and crystallinity of 70 to 80 %.
[0061] If the tensile strength is more than 6 g/d, the tensile modulus is more than 80 g/d,
or the elongation at break is less than 14 %, not only is the weavability of the polyethylene
yarn not good, but also the fabric produced using the yarn is excessively stiff, such
that the user may feel discomfort. Conversely, if the tensile strength is 4 g/d or
less, the tensile modulus is less than 15 g/d, or the elongation at break exceeds
55 %, pills may form on fabrics and even breakage of the fabric occurs when the user
continuously uses fabrics made from these polyethylene yarns.
[0062] If the crystallinity of the polyethylene yarn is less than 60 %, its thermal conductivity
is low, and thus the fabric made therefrom cannot provide the user with a sufficient
cooling sensation. That is, since the polyethylene yarn has crystallinity of 60 to
85 %, the skin cooling fabric produced using the same may have thermal conductivity
in the thickness direction of 0.0001 W/cm· °C or more, a heat transfer coefficient
in the thickness direction of 0.001 W/cm
2· °C or more at 20 °C, and a contact cold sensation (Qmax) of 0.1 W/cm
2 or more.
[0063] The polyethylene yarn according to an embodiment of the present invention has a weight
average molecular weight (Mw) of 50,000 to 99,000 g/mol. The weight average molecular
weight (Mw) of the polyethylene yarn is closely related to the physical properties
of polyethylene used as a raw material.
[0064] The polyethylene yarn of the present invention may have a DPF (Denier Per Filament)
of 1 to 5. That is, the polyethylene yarn may include a plurality of filaments each
having a fineness of 1 to 5 denier. In addition, the polyethylene yarn of the present
invention may have total fineness of 75 to 450 denier.
[0065] In a polyethylene yarn having a predetermined total fineness, if the fineness of
each filament exceeds 5 denier, the smoothness of the fabric made form the polyethylene
yarn becomes insufficient and the contact area with the body becomes small, thus making
it impossible to provide a user with a sufficient cooling sensation. In general, the
DPF can be adjusted through the discharge amount per hole of a spinneret (hereinafter,
referred to as the "single-hole discharge amount") and the draw ratio.
[0066] The polyethylene yarn of the present invention may have a circular cross-section
or a non-circular cross-section, but it is desirable to have a circular cross-section
from the viewpoint that it can provide an uniform cooling sensation to the user.
[0067] The skin cooling fabric of the present invention made from the polyethylene yarn
described above may be a woven or knitted fabric having a weight per unit area (i.e.,
area density) of 75 to 800 g/m
2. If the area density of the fabric is less than 75 g/m
2, the denseness of the fabric will be insufficient and there will be many voids in
the fabric. These voids reduce the cooling sensation of the fabric. On the other hand,
if the area density of the fabric exceeds 800 g/m
2, the fabric is very stiff due to the excessively dense fabric structure, causing
a problem in the tactile sensation felt by the user, and the high weight causes a
problem in use.
[0068] According to one embodiment of the present invention, the skin cooling fabric of
the present invention includes the above-mentioned polyethylene yarns of the present
invention as a warp yarn and a weft yarn, and may be a fabric having a cover factor
of 400 to 2000 according to Equation 2 below.

[0069] In Equation 2, CF is a cover factor, W
D is a warp density (ea/inch), W
T is a weft fineness (denier), F
D is a weft density (ea/inch), and F
T is a weft fineness (denier).
[0070] If the cover factor is less than 400, there is a problem that the denseness of the
fabric is insufficient, and the cooling sensation of the fabric is lowered due to
too many voids existing in the fabric. On the other hand, if the cover factor is more
than 2000, the denseness of the fabric is excessively high, the tactile sensation
of the fabric becomes worse, and a problem in use can occur due to the high fabric
weight.
[0071] The skin cooling fabric of the present invention has the following features:
- (i) dry thermal shrinkage rates in the directions of warp and weft after heat treatment
in a chamber at 70 °C for 15 minutes are 0.1 to 1.0 %, 0.2 to 0.8 %, or 0.25 to 0.45
%, respectively,
- (ii) dry thermal shrinkage rates in the directions of warp and weft after heat treatment
in a chamber at 100 °C for 15 minutes are 0.3 to 1.2 %, 0.5 to 1.0 %, or 0.75 to 0.95
%, respectively, and
- (iii) wet thermal shrinkage rates in the directions of warp and weft after immersion
in hot water at 100 °C for 30 minutes are 0.2 to 1.0 %, 0.5 to 1.0 %, or 0.65 to 0.85
%.
[0072] The dry thermal shrinkage rate and the wet thermal shrinkage rate of the fabric are
measured according to the ASTM D 1776 method.
[0073] The skin cooling fabric according to one embodiment of the present invention has,
at 20 °C:
- (i) thermal conductivity in the thickness direction of 0.0001 W/cm· °C or higher,
or 0.0003 to 0.0005 W/cm· °C;
- (ii) a heat transfer coefficient in the thickness direction of 0.001 W/cm2· °C or higher, or 0.01 to 0.02 W/cm2· °C; and
- (iii) a contact cold sensation (Qmax) of 0.1 W/cm2 or more, 0.1 to 0.3 W/cm2, or 0.1 to 0.2 W/cm2.
[0074] The measurement method of the thermal conductivity, heat transfer coefficient, and
contact cold sensation (Q
max) of the fabric will be described later.
[0075] In order to manufacture polyethylene yarns having the above-mentioned shrinkage properties,
tensile strength, tensile modulus, elongation at break, and crystallinity, not only
process factors such as (i) the spinning temperature, (ii) the L/D of the spinneret,
(iii) the discharge linear velocity from the spinneret of the molten polyethylene,
(iv) the distance from the spinneret to the multistage drawing part [specifically,
the first godet roller part of a multistage drawing part], (v) cooling conditions,
and (vi) spinning speed, etc., should be precisely controlled, but it is also necessary
to select a raw material having physical properties that are suitable for the present
invention.
[0076] Hereinafter, a method for manufacturing a polyethylene yarn for a skin cooling fabric
of the present invention will be described in detail with reference to FIG. 1.
[0077] First, a chip-shaped polyethylene is injected into an extruder 100 and melted.
[0078] The polyethylene used as a raw material for the manufacture of the polyethylene yarn
of the present invention has a density of 0.941 to 0.965 g/cm
3, a weight average molecular weight (Mw) of 50,000 to 99,000 g/mol, and a melt index
(MI) (at 190 °C) of 6 to 21 g/10 min.
[0079] In order to manufacture a fabric that provides a high cooling sensation, the polyethylene
yarn needs to have a high crystallinity of 60 to 85 %, and in order to manufacture
a polyethylene yarn having such a high crystallinity, it is essential to use a high
density polyethylene (HDPE) having a density of 0.941 to 0.965 g/cm
3.
[0080] When the weight average molecular weight (Mw) of polyethylene used as a raw material
is less than 50,000 g/mol, the finally obtained polyethylene yarn is made difficult
to express a strength of 4 g/d or more and a tensile modulus of 15 g/d or more, and
as a result, pills may form on fabrics. On the contrary, when the weight average molecular
weight (Mw) of the polyethylene exceeds 99,000 g/mol, the weavability of polyethylene
yarn is not good due to the excessively high strength and tensile modulus, the stiffness
is too high, and it is unsuitable for use in the manufacture of skin cooling fabrics
that are intended for contacting with the user's skin.
[0081] When the melt index (MI) of polyethylene used as a raw material is less than 6 g/10
min, it is difficult to ensure smooth flowability in an extruder 100 due to the high
viscosity and low flowability of the molten polyethylene, and the uniformity and processability
of the extrudate are reduced, thus increasing the risk of yarn breakage during the
spinning process. On the other hand, when the melt index (MI) of the polyethylene
exceeds 21 g/10min, the flowability in the extruder 100 becomes relatively good, but
it may be difficult for the finally obtained polyethylene yarn to have strength of
greater than 4 g/d and a tensile modulus of 15 g/d or more.
[0082] Optionally, a fluorine-based polymer can be added to polyethylene.
[0083] As the method of adding the fluorine-based polymer, (i) a method of injecting a master
batch containing polyethylene and a fluorine-based polymer together with a polyethylene
chip into the extruder 100 and then melting them therein, or (ii) a method of injecting
the fluorine-based polymer into an extruder 100 through a side feeder while injecting
the polyethylene chip into the extruder 100, and then melting them together, may be
mentioned.
[0084] By adding a fluorine-based polymer to the polyethylene, the occurrence of yarn breakage
during the spinning process and the multistage stretching process can be further suppressed,
and thus the productivity can be further improved. As a nonlimiting example, the fluorine-based
polymer added to the polyethylene may be a tetrafluoroethylene copolymer. The fluorine-based
polymer may be added to the polyethylene in such amount that the content of fluorine
in the finally produced yarn becomes 50 to 2500 ppm.
[0085] After the polyethylene having the above-described physical properties is injected
into the extruder 100 and melted, the molten polyethylene is transferred to a spinneret
200 by a screw (not shown) in the extruder 100, and extruded through a plurality of
spinning holes formed in the spinneret 200.
[0086] The number of holes in the spinneret 200 may be determined according to the DPF and
the total fineness of the produced yarn. For example, when manufacturing a yarn having
total fineness of 75 denier, the spinneret 200 may have 20 to 75 holes. Further, when
manufacturing a yarn having total fineness of 450 denier, the spinneret 200 may have
90 to 450 holes, preferably 100 to 400 holes.
[0087] The melting step in the extruder 100 and the extrusion step through the spinneret
200 are preferably performed at 150 to 315 °C, preferably 250 to 315 °C, more preferably
265 to 310 °C. That is, the extruder 100 and the spinneret 200 are preferably maintained
at 150 to 315 °C, preferably 250 to 315 °C, more preferably 265 to 310 °C.
[0088] When the spinning temperature is less than 150 °C, the spinning temperature is low
so that the HDPE may not be uniformly melted and thus spinning may be difficult. On
the other hand, when the spinning temperature exceeds 315 °C, the polyethylene may
be thermally decomposed and it may be difficult to express the high strength.
[0089] L/D, which is the ratio of the hole length L to the hole diameter D of the spinneret
200, may be 3 to 40. When L/D is less than 3, a die swell phenomenon occurs during
melt extrusion, and it becomes difficult to control the elastic behavior of polyethylene,
resulting in a poor spinning property. Further, when the L/D exceeds 40, a non-uniform
discharge phenomenon may occur due to a pressure drop along with yarn breakage caused
by a necking phenomenon of the molten polyethylene passing through the spinneret 200.
[0090] As the molten polyethylene is discharged from the holes of the spinneret 200, the
solidification of the polyethylene is started by the difference between the spinning
temperature and the ambient temperature, and simultaneously a semi-solidified filament
is formed. In this specification, not only the semi-solidified filament but also the
completely solidified filament are collectively referred to as "filament".
[0091] The plurality of filaments 11 are completely solidified by being cooled in a quenching
zone 300. The cooling of the filaments 11 may be performed by an air cooling method.
[0092] In the quenching zone 300, the cooling of the filaments 11 is preferably performed
so as to be cooled to 15 to 40 °C using cooling air having a wind speed of 0.2 to
1 m/s. When the cooling temperature is less than 15 °C, the elongation may be insufficient
due to over-cooling, which may cause yarn breakage in the drawing process. When the
cooling temperature exceeds 40 °C, the fineness deviation between filaments 11 increases
due to non-uniform solidification which may cause yarn breakage in the drawing process.
[0093] Subsequently, the filaments 11 that are cooled and completely solidified are converged
by a converging part 400 to form a multifilament 10.
[0094] As illustrated in FIG. 1, the method of the present invention may further include
a step of applying an emulsion onto the cooled filaments 11 using an oil roller (OR)
or oil jet, before forming the multifilament 10. The emulsion applying step may be
performed through a metered oiling (MO) method.
[0095] Optionally, the step of forming the multifilament 10 through a converging part 400
and the step of applying the emulsion may be performed at the same time.
[0096] The oil may be applied to the filaments 11 according to the dual roller system, which
is a two-stage system. In the case of this system, the amount of oil pick-up (OPU)
can be adjusted to 1 to 4 wt% by setting the rotation speed to 5 to 20 rpm.
[0097] As illustrated in FIG. 1, the polyethylene yarn of the present invention may be produced
via a direct spinning drawing (DSD) process. The multifilament 10 is directly transferred
to a multistage drawing part 500 including a plurality of godet roller parts GR1...
GRn and multistage-drawn at a total draw ratio of 2.5 to 8.5, preferably 3.5 to 7.5,
and then wound on a winder 600.
[0098] Alternatively, after the multifilament 10 is first wound as an undrawn yarn, the
undrawn yarn can be drawn, thereby manufacturing the polyethylene yarn of the present
invention. The polyethylene yarn of the present invention may be manufactured through
a two-step process of first melt spinning polyethylene to produce an undrawn yarn
and then drawing the undrawn yarn.
[0099] If the total draw ratio applied in the drawing process is less than 3.5, in particular,
less than 2.5, (i) the finally obtained polyethylene yarn cannot have crystallinity
of 60 % or more, and thus the fabric made from the yarn cannot provide a user with
a sufficient cooling sensation, and (ii) the polyethylene yarn cannot have strength
of greater than 4 g/d, a tensile modulus of 15 g/d or more, and elongation at break
of 55 % or less, and as a result, pills may form on the fabric produced from the yarn.
[0100] On the other hand, when the total draw ratio is greater than 7.5, in particular,
greater than 8.5, the finally obtained polyethylene yarn cannot have strength of 6
g/d or less, a tensile modulus of 80 g/d or less, and elongation at break of 14 %
or more. Therefore, not only is the weavability of the polyethylene yarn not good,
but also the fabric produced using the yarn becomes excessively stiff, thus making
the user feel discomfort.
[0101] If the linear velocity of the first godet roller part (GR1) that determines the spinning
speed of the melt spinning of the present invention is determined, the linear velocity
of the remaining godet roller parts is appropriately determined so that in the multistage
drawing part 500, a total draw ratio of 2.5 to 8.5, preferably 3.5 to 7.5, can be
applied to the multifilament 10.
[0102] According to one embodiment of the present invention, by appropriately setting the
temperature of the godet roller parts (GR1... GRn) of the multistage drawing part
500 in the range of 40 to 140 °C, heat-setting of the polyethylene yarn may be performed
through the multistage drawing part 500.
[0103] For example, the temperature of the first godet roller part (GR1) may be 40 to 80
°C, and the temperature of the last godet roller part (GRn) may be 110 to 140 °C.
The temperature of each of the godet roller parts excluding the first and last godet
roller parts (GR1, GRn) may be set to be equal to or higher than the temperature of
the godet roller part immediately before. The temperature of the last godet roller
part (GRn) may be set to be equal to or higher than the temperature of the godet roller
part immediately before, but may be set slightly lower than that temperature.
[0104] Interlacing of the multifilament 10 that has passed through the multistage drawing
part 500 may be performed. In this case, the nozzle pressure of an interlacing apparatus
is adjusted so that the number of interlacings may be 10 to 40 ea/m.
[0105] After the interlacing step, the multifilament 10 is wound on the winder 600, thereby
completing the manufacture of the polyethylene yarn for a skin cooling fabric of the
present invention.
[0106] As described above, when the interlacing step is performed with a high number of
interlacings of 10 to 40 ea/m, it is possible to satisfy the required convergence
without a separate twisting step, but in order to further improve the convergence
of the filaments, a step of twisting the polyethylene yarn with a twist number of
50 to 300 TPM (twists per meter) in the Z direction may be further performed in addition
to the interlacing step.
[0107] In order to ensure the low shrinkage rate of the polyethylene yarn of the present
invention, it is important to control the tension between the last roller (GRn) of
the multistage drawing part 500 and the winder 600. According to the present invention,
the over feed ratio defined by Equation 1 below is 6 to 10 %.

in Equation 1, OFR is the overfeed ratio, V
1 is the speed of the last godet roller (GRn), and V
2 is the speed of the winder 600.
[0108] Hereinafter, the present invention will be described in more detail by way concrete
examples. However, these examples are only to aid the understanding of the present
invention and the scope of the present invention is not limited thereto.
Example 1
[0109] A polyethylene yarn containing 200 filaments and having total fineness of 400 denier
was produced using the apparatus illustrated in FIG. 1. In detail, a polyethylene
chip having a density of 0.961 g/cm
3, a weight average molecular weight (Mw) of 87,660 g/mol, a polydispersity index (PDI)
[ratio (Mw/Mn) of weight average molecular weight (Mw) to number average molecular
weight (Mn)] of 6.4, and a melt index (MI at 190 °C) of 11.9 g/10 min was injected
into an extruder 100 and melted. The molten polyethylene was extruded through a spinneret
200 having 200 holes. L/D, which is the ratio of the hole length L to the hole diameter
D of the spinneret 200, was 5.0. The spinneret temperature was 270 °C.
[0110] The filaments 11 formed while being discharged from the spinneret 200 were finally
cooled to 25 °C by cooling air having a wind speed of 0.5 m/s in a quenching zone
300, and were converged into a multifilament 10 by the converging unit 400 and moved
to the multistage drawing part 500. Simultaneously with the converging step, a step
of applying oil through the MO (Metered Oiling) method was performed.
[0111] The multistage drawing part 500 was composed of a total of five stage godet rollers,
the temperature of the godet roller parts was set to 80 to 125 °C, and the temperature
of the rear stage roller part was set to be higher than the temperature of the roller
part immediately before.
[0112] After the multifilament 10 was drawn at a total draw ratio of 7.5 by the multistage
drawing part 500, 20 ea/m of interlacing was produced and wound on the winder 600
at an overfeed ratio of 6.5 %, thereby obtaining a polyethylene yarn with an OPU of
3 wt%.
Example 2
[0113] A polyethylene yarn was obtained in the same manner as in Example 1, except that
a polyethylene chip having a density of 0.958 g/cm
3, a weight average molecular weight (Mw) of 98,290 g/mol, a polydispersity index (PDI)
of 8.4, and a melt index (MI at 190 °C) of 6.1 g/10 min was used, the spinneret temperature
was 275 °C and the overfeed ratio was 7.5 %.
Example 3
[0114] A polyethylene yarn was obtained in the same manner as in Example 1, except that
a polyethylene chip having a density of 0.948 g/cm
3, a weight average molecular weight (Mw) of 78,620 g/mol, a polydispersity index (PDI)
of 8.2, and a melt index (MI at 190 °C) of 15.5 g/10 min was used, the spinneret temperature
was 260 °C, and the total draw ratio was 7.0.
Comparative Example 1
[0115] A polyethylene yarn was obtained in the same manner as in Example 1, except that
a polyethylene chip having a density of 0.962 g/cm
3, a weight average molecular weight (Mw) of 98,550 g/mol, a polydispersity index (PDI)
of 4.9, and a melt index (MI at 190 °C) of 6.1 g/10 min was used, the spinneret temperature
was 280 °C, and the overfeed ratio was 2.0 %.
Comparative Example 2
[0116] A polyethylene yarn was obtained in the same manner as in Example 1, except that
a polyethylene chip having a density of 0.961 g/cm
3, a weight average molecular weight (Mw) of 98,230 g/mol, a polydispersity index (PDI)
of 7.0, and a melt index (MI at 190 °C) of 2.9 g/10 min was used, the spinneret temperature
was 295 °C, the total draw ratio was 8.2, and the overfeed ratio was 3.0 %.
Comparative Example 3
[0117] A polyethylene yarn was obtained in the same manner as in Example 1, except that
a polyethylene chip having a density of 0.961 g/cm
3, a weight average molecular weight (Mw) of 180,550 g/mol, a polydispersity index
(PDI) of 6.4, and a melt index (MI at 190 °C) of 0.6 g/10 min was used, the spinneret
temperature was 295 °C, it was drawn at a total draw ratio of 14 through the multistage
drawing part 500 composed of a total of eight stage godet roller parts, the temperature
of the godet roller parts was set to 70 to 130 °C, and the overfeed ratio was 2.5
%.
Test Example 1
[0118] The shrinkage properties, toughness, tensile strength, tensile modulus, elongation
at break, and crystallinity of the polyethylene yarn prepared by each of Examples
1 to 3 and Comparative Examples 1 to 3 were respectively measured as follows, and
the results are shown in Table 1 and Table 2 below.
(1) Shrinkage stress of polyethylene yarn
[0119] The polyethylene yarn was cut to prepare a sample having a length of 1000 mm. A thermal
stress tester (Kanebo Eng., KE-2) was used to obtain a graph showing the shrinkage
stress of the sample according to the temperature rise. The initial load was 0.1 g/d
and the temperature rising rate was 2.5 °C/s. From the graph, the shrinkage stresses
at 70 °C and 100 °C were obtained, respectively.
(2) Dry thermal shrinkage rate of polyethylene yarn
[0120] The dry thermal shrinkage rate of the polyethylene yarn was measured using Testrite
MK-V (Testrite Ltd.). In detail, the polyethylene yarn was cut to prepare a sample
having a length (L
0) of 1000 mm. The sample was placed in air at 70 °C (or 100 °C) for 15 minutes under
a load of 0.1 g/d and removed, and then left at room temperature for 10 minutes. Then,
the length of the sample (i.e., length L
1 after shrinkage) was measured, and the dry thermal shrinkage rate at 70 °C (or 100
°C) was calculated by Equation 3 below.

where L
0 is the length before shrinkage, and L
1 is the length after shrinkage.
(3) Wet thermal shrinkage rate of polyethylene yarn
[0121] The polyethylene yarn was cut to prepare a sample having a length (L
0) of 1000 mm. The sample was completely immersed in hot water at 100 °C for 30 minutes
under a load of 0.1 g/d and removed, and then left at room temperature for 120 minutes.
Then, the length of the sample (i.e., length L
1 after shrinkage) was measured, and the wet thermal shrinkage rate was calculated
by Equation 4 below.

where L
0 is the length before shrinkage, and L
1 is the length after shrinkage.
(4) Tensile strength, tensile modulus, elongation at break, and toughness of polyethylene
yarn
[0122] The tensile strength, tensile modulus, and elongation at break of the polyethylene
yarns were determined using an Instron universal tensile tester (Instron Engineering
Corp., Canton, Mass) in accordance with ASTM D885 (sample length: 250 mm, tensile
speed: 300 mm/min, and initial load: 0.05 g/d).
(5) Crystallization of polyethylene yarn
[0123] The crystallinity of the polyethylene yarn was measured using an XRD instrument (X-ray
diffractometer) (manufacturer: PANalytical, model name: EMPYREAN). In detail, the
polyethylene yarn was cut to prepare a sample having a length of 2.5 cm. The sample
was fixed to a sample holder and then measurement was performed under the following
conditions.
- Light source (X-ray source): Cu-Kα radiation
- Power: 45 KV × 25 mA
- Mode: continuous scan mode
- Scan angle range: 10° to 40°
- Scan speed: 0.1 °/s
[Table 1]
|
Example 1 |
Example 2 |
Example 3 |
PE |
Density (g/cm3) |
0.961 |
0.958 |
0.948 |
Mw (g/mol) |
87,660 |
98,290 |
78,620 |
PDI |
6.4 |
8.4 |
8.2 |
MI (g/10min) |
11.9 |
6.1 |
15.5 |
Spinneret temperature (°C) |
270 |
275 |
260 |
Total draw ratio |
7.5 |
7.5 |
7.0 |
Over feed ratio (%) |
6.5 |
7.5 |
6.5 |
PE yarn |
Shrinkage stress (g/d) at 70 °C |
0.008 |
0.011 |
0.007 |
Shrinkage stress (g/d) at 100 °C |
0.035 |
0.045 |
0.034 |
Dry thermal shrinkage rate (%) at 70 °C |
0.25 |
0.35 |
0.23 |
Dry thermal shrinkage rate (%) at 100 °C |
0.85 |
0.97 |
0.83 |
Wet thermal shrinkage rate (%) at 100 °C |
0.72 |
0.85 |
0.70 |
Tensile strength (g/d) |
4.6 |
5.3 |
4.5 |
Tensile modulus (g/d) |
49.6 |
56.3 |
44.6 |
Elongation at break (%) |
25 |
22 |
26 |
Crystallinity (%) |
72 |
74 |
71 |
[Table 2]
|
Com parative Example 1 |
Com parative Example 2 |
Com parative Example 3 |
PE |
Density (g/cm3) |
0.962 |
0.961 |
0.961 |
Mw /mol |
98,550 |
98,230 |
180,550 |
PDI |
4.9 |
7.0 |
6.4 |
MI (g/10min) |
6.1 |
2.9 |
0.6 |
Spinneret temperature (°C) |
280 |
295 |
295 |
Total draw ratio |
7.5 |
8.2 |
14.5 |
Over feed ratio (%) |
2.0 |
3.0 |
2.5 |
PE yarn |
Shrinkage stress (g/d) at 70 °C |
0.025 |
0.038 |
0.052 |
Shrinkage stress (g/d) at 100 °C |
0.083 |
0.092 |
0.125 |
Dry thermal shrinkage rate (%) at 70 °C |
0.65 |
0.72 |
0.93 |
Dry thermal shrinkage rate (%) at 100 °C |
1.65 |
1.75 |
2.2 |
Wet thermal shrinkage rate (%) at 100 °C |
1.2 |
1.4 |
1.7 |
|
Tensile strength (g/d) |
6.5 |
7.1 |
18.0 |
Tensile modulus (g/d) |
63.4 |
67.2 |
493 |
Elongation at break (%) |
13.5 |
12.7 |
6.0 |
Crystallinity (%) |
73 |
73 |
80 |
Example 4
[0124] The plain weave was performed using the polyethylene yarn of Example 1 as a warp
yarn and a weft yarn, thereby manufacturing a fabric having a warp density of 30 ea/inch
and a weft density of 30 ea/inch.
Example 5
[0125] A fabric was manufactured in the same manner as in Example 4, except that the polyethylene
yarn of Example 2 was used instead of the polyethylene yarn of Example 1.
Example 6
[0126] A fabric was manufactured in the same manner as in Example 4, except that the polyethylene
yarn of Example 3 was used instead of the polyethylene yarn of Example 1.
Comparative Example 4
[0127] A fabric was manufactured in the same manner as in Example 4, except that the polyethylene
yarn of Comparative Example 1 was used instead of the polyethylene yarn of Example
1.
Comparative Example 5
[0128] A fabric was manufactured in the same manner as in Example 4, except that the polyethylene
yarn of Comparative Example 2 was used instead of the polyethylene yarn of Example
1.
Comparative Example 6
[0129] A fabric was manufactured in the same manner as in Example 4, except that the polyethylene
yarn of Comparative Example 3 was used instead of the polyethylene yarn of Example
1.
Test Example 2
[0130] The contact cold sensation (Q
max), thermal conductivity (thickness direction), heat transfer coefficient (thickness
direction), stiffness, dry thermal shrinkage rate (at 70 °C & 100 °C), and wet thermal
shrinkage rate (at 100 °C) of the fabrics respectively manufactured by Examples 4
to 6 and Comparative Examples 4 to 6 were measured as follows, and the results are
shown in Tables 3 and 4 below.
(1) Contact cold sensation (Qmax) of fabric
[0131] A fabric sample having a size of 20 cm × 20 cm was prepared, and then allowed to
stand for 24 hours under the conditions of a temperature of 20 ± 2 °C and a RH of
65 ± 2 %. Then, the contact cold sensation (Q
max) of the fabric was measured using a KES-F7 THERMO LABO II (Kato Tech Co., LTD.) apparatus
under the test environment of a temperature of 20 ± 2 °C and 65 ± 2 % RH.
[0132] In detail, as illustrated in FIG. 2, the fabric sample 23 was placed on a base plate
(also referred to as "Water-Box") 21 maintained at 20 °C, and a T-Box 22a (contact
area: 3 cm × 3 cm) heated to 30 °C was placed on the fabric sample 23 for only 1 second.
That is, the other surface of the fabric sample 23 whose one surface was in contact
with the base plate 21 was brought into instantaneous contact with the T-Box 22a.
The contact pressure applied to the fabric sample 23 by the T-Box 22a was 6 gf/cm
2. Then, the Q
max value displayed on a monitor (not shown) connected to the apparatus was recorded.
Such a test was repeated 10 times and the arithmetic mean value of the obtained Qmax
values was calculated.
(2) Thermal conductivity and heat transfer coefficient of fabric
[0133] A fabric sample having a size of 20 cm × 20 cm was prepared and then allowed to stand
for 24 hours under the conditions of a temperature of 20 ± 2 °C and a RH of 65 ± 2
%. Then, the thermal conductivity and heat transfer coefficient of the fabric were
measured using a KES-F7 THERMO LABO II (Kato Tech Co., LTD.) apparatus under the test
environment of a temperature of 20 ± 2 °C and 65 ± 2 % RH.
[0134] In detail, as illustrated in FIG. 3, the fabric sample 23 was placed on a base plate
21 maintained at 20 °C, and the T-Box 22b (contact area: 5 cm × 5 cm) heated to 30
°C was placed on the fabric sample 23 for 1 minute. Even while the BT-Box 22b was
in contact with the fabric sample 23, heat was continuously supplied to the BT-Box
22b so that the temperature could be maintained at 30 °C. The amount of heat (i.e.,
heat flow loss) supplied to maintain the temperature of the BT-Box 22b was displayed
on a monitor (not shown) connected to the apparatus. Such a test was repeated 5 times
and the arithmetic mean value of the obtained heat flow loss was calculated. Then,
the thermal conductivity and the heat transfer coefficient of the fabric were calculated
using Equations 5 and 6 below.

where K is a thermal conductivity (W/cm· °C), D is a thickness (cm) of the fabric
sample 23, A is a contact area (= 25 cm
2) of the BT-Box 22b, ΔT is a temperature difference (= 10 °C) on both sides of the
fabric sample 23, W is a heat flow loss (Watt), and k is a heat transfer coefficient
(W/cm
2· °C).
(3) Stiffness of fabric
[0135] The stiffness of the fabric was measured by the circular bend method using a stiffness
measuring device in accordance with ASTM D 4032. As the stiffness (kgf) is lower,
the fabric has softer properties.
(4) Dry thermal shrinkage rate of fabric
[0136] A fabric was cut to prepare a sample having a size of 20 cm x 20 cm (warp direction
length x weft direction length). Lines having a length of 20 cm (i.e., "length before
shrinkage", L
0) in the warp and weft directions were marked on the sample, respectively. The sample
was heat-treated in a chamber at 70 °C (or 100 °C) for 15 minutes and then left at
ambient temperature for 10 minutes. Then, the lengths of the lines displayed on the
sample (i.e., "length after shrinkage", L
1) were respectively measured, and the dry thermal shrinkage rate at 70 °C (or 100
°C) was calculated by Equation 7 below with respect to each of the warp direction
and the weft direction.

where L
0 is "length before shrinkage" (i.e., 20 cm) and L
1 is "length after shrinkage".
(5) Wet thermal shrinkage rate of fabric
[0137] A fabric was cut to prepare a sample having a size of 20 cm × 20 cm (warp direction
length × weft direction length). Lines having a length of 20 cm (i.e., "length before
shrinkage", L
0) in the warp and weft directions were marked on the sample, respectively. The sample
was treated with hot water at 100 °C for 30 minutes using an IR dyeing machine, and
then left at ambient temperature for 120 minutes. Then, the lengths of the lines displayed
on the sample (i.e., "length after shrinkage", L
1) were respectively measured, and the wet thermal shrinkage rate was calculated by
Equation 8 below with respect to each of the warp direction and the weft direction.

where L
0 is "length before shrinkage" (i.e., 20 cm) and L
1 is "length after shrinkage".
[Table 3]
|
Example 4 |
Example 5 |
Example 6 |
Qmax (W/cm2) |
0.158 |
0.165 |
0.148 |
Thermal conductivity (W/cm· °C) |
0.00042 |
0.00048 |
0.00037 |
Heat transfer coefficient (W/cm2· °C) |
0.0124 |
0.0142 |
0.0122 |
Stiffness (kgf) |
0.45 |
0.52 |
0.43 |
Dry thermal shrinkage rate (%) at 70 °C |
Warp direction |
0.35 |
0.45 |
0.33 |
Weft direction |
0.32 |
0.42 |
0.29 |
Dry thermal shrinkage rate (%) at 100 °C |
Warp direction |
0.85 |
0.93 |
0.82 |
Weft direction |
0.80 |
0.88 |
0.76 |
Wet thermal shrinkage rate (%) at 100 °C |
Warp direction |
0.75 |
0.83 |
0.73 |
Weft direction |
0.70 |
0.76 |
0.66 |
[Table 4]
|
Com parative Example 4 |
Com parative Example 5 |
Com parative Example 6 |
Qmax (W/cm2) |
0.165 |
0.168 |
0.169 |
Thermal conductivity (W/cm· °C) |
0.00056 |
0.00060 |
0.00064 |
Heat transfer coefficient (W/cm2· °C) |
0.00148 |
0.00150 |
0.00155 |
Stiffness (kgf) |
0.65 |
0.72 |
0.95 |
Dry thermal shrinkage rate (%) at 70 °C |
Warp direction |
1.05 |
1.18 |
1.45 |
Weft direction |
1.02 |
1.13 |
1.39 |
Dry thermal shrinkage rate (%) at 100 °C |
Warp direction |
1.35 |
1.48 |
1.88 |
Weft direction |
1.25 |
1.33 |
1.68 |
Wet thermal shrinkage rate (%) at 100 °C |
Warp direction |
1.3 |
1.55 |
2.0 |
Weft direction |
1.18 |
1.44 |
1.82 |
[Explanation of Symbols]
100: |
extruder |
200: |
spinneret |
300: |
quenching zone |
11: |
filaments |
OR: |
oil roller |
400: |
converging part |
10: |
multifilament |
500: |
multistage drawing part |
GR1: |
first godet roller part |
GRn: |
last godet roller part |
600: |
winder |
21: |
base plate |
22a: |
T-Box |
22b: |
BT-Box |
23: |
fabric sample |
|
|