[Technical Field]
[0001] The following disclosure relates to a dope dyed polyethylene yarn and a functional
fabric including the same, and more particularly, to a dope dyed polyethylene yarn
having excellent color uniformity and a functional fabric including the same.
[Background Art]
[0002] A high-density polyethylene (HDPE) yarn refers to a high-strength polyethylene yarn
having a density of 0.94 g/cm
3 or more. The high-density polyethylene yarn has been used in various materials for
sports ropes, fishing lines, protective clothes, bulletproof clothes, stab proof clothes,
and the like requiring a high strength, and also has been applied to various composite
materials requiring an ultrahigh strength.
[0003] In addition, the high-density polyethylene yarn has a high thermal conductivity by
lattice vibration called phonon, and has excellent lightness because it has a specific
gravity of about 0.93 and is light enough to float on water.
[0004] Therefore, the high-density polyethylene yarn has been widely used for summer clothes,
work clothes, sportswear, and the like requiring a cooling sensation, as well as the
textile products requiring a high strength, such as sports ropes, fishing lines, protective
clothes, bulletproof clothes, and stab proof clothes.
[0005] However, the high-density polyethylene yarn is known as a flame retardant fiber because
it is nearly impossible to dye even using any dye in a dyeing system due to its hydrophobicity
caused by high crystallinity.
[0006] Two kinds of coloring methods are currently used to dye the high-density polyethylene
yarn. One is a dope dyeing method in which spinning is performed by adding a pigment,
and the other one is a polymer blend method in which different dyeable polymers are
mixed.
[0007] However, a dope dyed polyethylene yarn manufactured by the polymer blend method has
a disadvantage in that it is difficult to maintain the specific physical properties
of the high-density polyethylene yarn, such as a high thermal conductivity and lightness,
because the polymers having different physical properties are mixed in addition to
polyethylene.
[0008] Therefore, as disclosed in
Korean Patent No. 10-1992444 "Method of Manufacturing Dope Dyed Polyethylene Multi-Filament False-Twist Yarn",
a dope dyed polyethylene yarn manufactured by a dope dyeing method of melt spinning
a masterbatch chip to which a pigment is added has been used in the related art.
[0009] However, in the dope dyed polyethylene yarn according to the related art, it is difficult
for the pigment to be uniformly mixed with polyethylene having a relatively high viscosity,
and color unevenness of the yarn due to the non-uniformity of mixing between the pigment
and the polyethylene raw material is serious. Therefore, the quality is degraded due
to the non-uniformity of the dope dyed yarn itself, and physical properties of the
yarn such as a strength are deteriorated as a large amount of pigment is added in
order to express a desired color. Furthermore, the quality of the final product manufactured
using the yarn is also degraded.
[DETAILED DESCRIPTION OF THE INVENTION]
[Technical Problem]
[0010] An embodiment of the present invention is directed to providing a dope dyed polyethylene
yarn having excellent color uniformity and a functional fabric including the same.
[Technical Solution]
[0011] In one general aspect, a dope dyed polyethylene yarn contains a pigment, wherein
L*, a* and b* measured under the following measurement condition satisfy the following
expression:
[Measurement condition]
[0012] a measurement region is formed by winding the dope dyed polyethylene yarn around
a planar substrate, computer color matching (CCM) is measured in the measurement region,
and the CCM is measured at least n times (n is a natural number of 50 or more) every
time the dope dyed polyethylene yarn is wound around the substrate 70 turns,

wherein C
max, C
min, and C
aver represent maximum, minimum, and average values of any one selected from L*, a*, and
b*, respectively.
[0013] In the dyed polyethylene yarn according to an embodiment of the present invention,
when the CCM of the dope dyed polyethylene yarn is measured, a standard deviation
of values of L* may be 3 or less.
[0014] In the dope-dyed polyethylene yarn according to an embodiment of the present invention,
the pigment may be contained in an amount of 0.00005 to 1 wt% with respect to a total
weight of the dope dyed polyethylene yarn.
[0015] In the dyed polyethylene yarn according to an embodiment of the present invention,
a degree of crystallinity of the dope dyed polyethylene yarn may be 60 to 80%.
[0016] In the dyed polyethylene yarn according to an embodiment of the present invention,
the dope dyed polyethylene yarn may have an initial modulus of 10 to 300 cN/dtex and
a strength of 1.5 to 20 g/d when measured according to ASTM D2256.
[0017] In the dope-dyed polyethylene yarn according to an embodiment of the present invention,
the dope dyed polyethylene yarn may have a melt index (Ml, @190°C) of 0.5 to 22 g/10
min when measured according to ASTM D1238.
[0018] In the dyed polyethylene yarn according to an embodiment of the present invention,
the dope dyed polyethylene yarn may have a dry heat shrinkage rate (@100°C) of 2 to
15% when measured according to ASTM D4974-04.
[0019] A functional fabric according to the present invention is manufactured using the
dope dyed polyethylene yarn.
[0020] In the functional fabric according to an embodiment of the present invention, the
functional fabric may have a contact cooling sensation of 0.1 to 0.3 W/cm
2 when measured by bringing a heat plate (T-box) at 30 ± 2°C into contact with the
functional fabric at 20 ± 2°C at 20 ± 2°C and 65 ± 2% R.H.
according to an embodiment of the present invention, the functional fabric may have
a thermal conductivity in a thickness direction of 0.05 to 0.25 W/mK when measured
by bringing a heat source plate (BT-box) at 30 ± 2°C into contact with the functional
fabric at 20 ± 2°C at 20 ± 2°C and 65 ± 2% R.H.
[Advantageous Effects]
[0021] As set forth above, the polyethylene yarn according to the present invention has
excellent color uniformity, such that coloring characteristics may be excellent compared
to the amount of pigment added.
[0022] Further, the polyethylene yarn according to the present invention may maintain the
inherent excellent thermal conductivity of high-density polyethylene in spite of addition
of a pigment, such that a fabric having an excellent cooling sensation may be manufactured.
[0023] Further, the functional fabric according to the present invention includes a polyethylene
yarn having excellent color uniformity and an excellent thermal conductivity, such
that the functional fabric may have excellent coloring characteristics and color uniformity
and may have a cooling sensation.
[Brief Description of Drawings]
[0024]
FIG. 1 is a schematic view illustrating a process of manufacturing a yarn according
to an exemplary embodiment of the present invention.
FIG. 2 is a photograph of an apparatus for measuring computer color matching (CCM)
of a functional fabric according to an exemplary embodiment of the present invention.
FIG. 3 is a schematic view illustrating an apparatus for measuring a contact cooling
sensation of the functional fabric according to an exemplary embodiment of the present
invention.
FIG. 4 is a schematic view illustrating an apparatus for measuring a thermal conductivity
in a thickness direction of the functional fabric according to an exemplary embodiment
of the present invention.
FIG. 5 illustrates a result of measuring the CCM of the yarn according to an exemplary
embodiment of the present invention.
[DETAILED DESCRIPTION OF EMBODIMENTS]
[0025] Unless otherwise defined, all the technical terms and scientific terms used in the
present specification have the same meanings as commonly understood by those skilled
in the art to which the present invention pertains. The description for the known
function and configuration unnecessarily obscuring the gist of the present invention
will be omitted in the following description and the accompanying drawings.
[0026] In addition, unless the context clearly indicates otherwise, the singular forms used
in the present specification may be intended to include the plural forms.
[0027] In addition, units used in the present specification without special mention are
based on weight, and as an example, a unit of % or a ratio refers to wt% or a weight
ratio. Unless otherwise defined, wt% refers to wt% of any one component in a composition
with respect to the total weight of the composition.
[0028] In addition, a numerical range used in the present specification includes upper and
lower limits and all values within these limits, increments logically derived from
a form and span of a defined range, all double limited values, and all possible combinations
of the upper and lower limits in the numerical range defined in different forms. Unless
otherwise particularly defined in the present specification, all values out of the
numerical range that may occur due to the rounding off of the experimental errors
or values also fall within the defined numerical ranges.
[0029] In the present specification, the expression "comprise(s)" is intended to be an open-ended
transitional phrase having an equivalent meaning to "include(s)," "contain(s)," "have
(has)," and "is (are) characterized by," and does not exclude elements, materials,
or steps, all of which are not further recited herein.
[0030] In a dope dyed polyethylene yarn according to the related art, it is difficult for
a pigment to be uniformly mixed with polyethylene having a relatively high viscosity,
and color unevenness of the yarn due to non-uniformity of mixing between the pigment
and the polyethylene raw material is serious. Therefore, the quality is degraded due
to the non-uniformity of the dope dyed yarn itself, and physical properties of the
yarn such as a strength are deteriorated as a large amount of pigment is added in
order to express a desired color. Furthermore, the quality of the final product manufactured
using the yarn is also degraded.
[0031] Therefore, the present applicant has conducted intensive studies for a long period
of time to develop a polyethylene fiber having excellent color uniformity while maintaining
physical properties thereof. As a result, the present applicant has developed a novel
dope dyed polyethylene yarn having excellent color uniformity by increasing a mixing
degree between the pigment and the raw material of the polyethylene yarn.
[0032] Specifically, the dope dyed polyethylene yarn according to the present invention
is a dope dyed polyethylene yarn containing a pigment, wherein L*, a* and b* measured
under the following measurement condition satisfy the following expression:
[Measurement condition]
[0033] a measurement region is formed by winding the dope dyed polyethylene yarn around
a planar substrate, computer color matching (CCM) is measured in the measurement region,
and the CCM is measured at least n times (n is a natural number of 50 or more) every
time the dope dyed polyethylene yarn is wound around the substrate 70 turns,

wherein C
max, C
min, and C
aver represent maximum, minimum, and average values of any one selected from L*, a*, and
b*, respectively.
[0034] Specifically, in the expression, (C
max - C
min)/C
aver × 100 may be 0.1 to 8 and more specifically 3 to 7. The dope dyed polyethylene yarn
has excellent color uniformity, such that coloring characteristics may be excellent
compared to the amount of pigment added. In addition, although a small amount of pigment
is added, the dope dyed polyethylene yarn has excellent coloring characteristics,
such that the dope dyed polyethylene yarn may maintain the inherent excellent thermal
conductivity of high-density polyethylene, thereby manufacturing a fabric having an
excellent cooling sensation.
[0035] Specifically, a region covered with the dope dyed polyethylene yarn, that is, a measurement
region, is formed on the substrate, as the dope dyed polyethylene yarn is wound around
the planar substrate.
[0036] In this case, the dope dyed polyethylene yarn wound n-1 (n is a natural number of
2 or more) turns and the dope dyed polyethylene yarn wound n turns may be in contact
with each other so that they are wound around a perimeter of the substrate in one
direction of the substrate.
[0037] Since the measurement region is formed by covering the substrate with the dope dyed
polyethylene yarn, the measurement region exhibits a color similar to when the dope
dyed polyethylene yarn is made into a fabric. The measurement region is not limited
as long as it has an area in which the CCM may be measured. However, the area occupied
by the measurement region on the substrate may be appropriately adjusted according
to a size of the substrate, and a thickness and the number of turns of winding of
the dope dyed polyethylene yarn. As a non-limiting example, a measurement region may
be formed by winding a dope dyed polyethylene yarn having a thickness of 410 De around
a square planar substrate having a width of 6.5 cm, a length of 6.5 cm, and a height
of 0.5 cm, 30 turns or more, specifically, 40 to 100 turns, and more specifically,
50 to 90 turns.
[0038] In the measurement region formed by the method described above, when the n-1
th (n is a natural number of 2 or more) CCM is measured and then the n
th CCM is measured, a measurement region for measuring the n
th CCM may be formed on a measurement region formed for measuring the n-1
th CCM.
[0039] Hereinafter, it is assumed that the previously formed measurement region is a first
measurement region, and the subsequently formed measurement is a second measurement
region.
[0040] CCM is measured in the first measurement region formed by winding the dope dyed polyethylene
yarn around the substrate 70 turns in one direction of the substrate, and then, CCM
is measured in the second measurement region formed by winding the dope dyed polyethylene
yarn around the first measurement region again. That is, the second measurement region
is formed by winding the dope dyed polyethylene yarn to cover the first measurement
region while a winding direction of the dope dyed polyethylene yarn is changed to
a direction opposite to the one direction of the substrate.
[0041] Therefore, the first measurement region in which the n-1
th CCM is measured and the second measurement region in which the n
th CCM is measured have the same size, and when the second measurement region is formed
on the first measurement region, a thickness of the measurement region formed on the
substrate is increased by the thickness of the dope dyed polyethylene yarn. In the
first measurement region and the second measurement region, the CCMs may be measured
at the same position.
[0042] L*, a* and b* of the CCM measured in the measurement region may satisfy the expression
described above.
[0043] Specifically, the pigment may be contained in an amount of 0.0001 to 0.5 wt%, specifically,
0.002 to 0.05 wt%, and more specifically, 0.01 to 0.03 wt%, with respect to the total
weight of the dope dyed polyethylene yarn, but the present invention is not limited
thereto. However, within the above range, the dope dyed polyethylene yarn may have
excellent coloring characteristics and color uniformity compared to the amount of
pigment added.
[0044] In this case, when the CCM of the yarn is measured, a standard deviation of values
of L* is 3 or less, specifically, 2 or less, and more specifically, 1.5 or less. Thus,
the dope dyed polyethylene yarn may have significantly excellent color uniformity
that is not easily distinguishable with the naked eye.
[0045] In the present invention, the pigment is not limited as long as it is a pigment or
a raw material used in dope dyeing of polyethylene according to the related art. As
a specific example, in a case of a black polyethylene yarn, the pigment may be carbon
black particles.
[0046] An initial modulus of the dope dyed polyethylene yarn may be 10 to 300 cN/dtex and
specifically50 to 300 cN/dtex, and more specifically 70 to 150 cN/dtex when measured
according to ASTM D2256. In this case, a strength of the dope dyed polyethylene yarn
may be, but is not limited to, 1.5 to 20 g/d, specifically 4 to 20 g/d and more specifically
10 to 15 g/d when measured according to ASTM D2256. However, within the above ranges,
the dope dyed polyethylene yarn may have a high thermal conductivity and a stiffness
suitable for weavability.
[0047] In addition, a polydispersity index of the dope dyed polyethylene yarn may be 5 to
20 and specifically 7 to 15, and in this case, a weight average molecular weight of
the dope dyed polyethylene yarn may be 45,000 to 300,000 g/mol and preferably 100,000
to 200,000 g/mol. Within the above ranges, when the yarn is melt-extruded, flowability
of a melt is preferable, occurrence of thermal decomposition is prevented, and processability
such as no yarn breakage during drawing is secured, such that a fabric having uniform
physical properties may be manufactured and a fabric having excellent durability may
be provided.
[0048] In addition, a melt index (Ml, @190°C) of the dope dyed polyethylene yarn may be
0.5 to 22 g/10 min, specifically, 1 to 10 g/10 min, and more specifically, 2 to 8
g/10 min, when measured at 190°C and 2.16 kg according to ASTM D1238. In addition,
a density of the dope dyed polyethylene yarn may be 0.93 to 0.97 g/cm
3. In addition, a degree of crystallinity of the dope dyed polyethylene yarn after
spinning may be 60 to 80% and specifically 65 to 75%. The degree of crystallinity
of the polyethylene yarn may be derived together with a crystallite size at the time
of crystallinity analysis using an X-ray diffractometer. As described above, when
the melt index, the density, and the degree of crystallinity are within the above
ranges, heat is rapidly diffused and dissipated by lattice vibration called phonon
in a direction of molecular chains linked via a covalent bond of high-density polyethylene
(HDPE), and a function of discharging moisture generated by sweating or breathing
is improved, such that a fabric having an excellent cooling sensation may be provided.
[0049] In addition, the dope dyed polyethylene yarn has a significantly low dry heat shrinkage
rate (@100°C) of 2 to 15% and specifically 2.7 to 5% when measured according to ASTM
D4974-04, such that the dope dyed polyethylene yarn may have excellent shape stability.
[0050] The dope dyed polyethylene yarn of the present invention may be manufactured by a
dope dyeing method.
[0051] Specifically, the dope dyed polyethylene yarn may be formed of a polyethylene resin
composition containing a color masterbatch, the color masterbatch being prepared by:
mixing a pigment with polyethylene in the form of a chip and performing drying to
prepare a first master chip; and repeating a process of melting and re-mixing the
first master chip and performing drying n times (n is a natural number of 1 or more)
to prepare the n
th master chip. In this case, n may be, but is not limited to, 2 to 5 and specifically
2 or 3. The polyethylene resin composition containing the color masterbatch prepared
as described above is prepared, such that the dope dyed polyethylene yarn may have
more excellent color uniformity.
[0052] A content of the pigment in the color masterbatch may be variously adjusted, and
the pigment may be contained in an amount of 0.05 to 10.0 wt% and specifically 0.1
to 5 wt% with respect to the total weight of the color masterbatch. Within the above
range, the dope dyed polyethylene yarn may have excellent coloring characteristics
in spite of a lower content of the pigment compared to a color masterbatch according
to the related art.
[0053] In addition, in the polyethylene resin composition containing the color masterbatch,
the color masterbatch may be appropriately mixed according to a content ratio of the
pigment in the yarn described above. Specifically, the color masterbatch may be contained
in an amount of 0.1 to 10 wt% with respect to the total weight of the polyethylene
resin composition.
[0054] The dope dyed polyethylene yarn manufactured by the dope dyeing method may have significantly
excellent color uniformity as described above, such that a high-quality fabric may
be provided.
[0055] Hereinafter, a method of manufacturing a dope dyed polyethylene yarn according to
an exemplary embodiment of the present invention will be described in detail with
reference to FIG. 1.
[0056] First, a first master chip is obtained by mixing a pigment with polyethylene in the
form of a chip, and then, the dried first master chip is melted again and re-mixed
to obtain a second master chip. Thereafter, a dope dyed polyethylene melt is obtained
by injecting the prepared second master chip and polyethylene in the form of a chip
into an extruder 100 and melting them.
[0057] The molten polyethylene is transported through a die 200 by a screw (not illustrated)
in the extruder 100, and the transported polyethylene is extruded through a plurality
of holes formed in the die 200. The number of holes of the die 200 may be determined
according to a denier per filament (DPF) and a fineness of a yarn to be manufactured.
For example, when a yarn having a total fineness of 75 denier is manufactured, the
die 200 may have 20 to 75 holes, and when a yarn having a total fineness of 450 denier
is manufactured, the die 200 may have 90 to 450 holes and preferably 100 to 400 holes.
[0058] The melting process performed in the extruder 100 and the extrusion process performed
in the die 200 may be changed and applied depending on a melt index of the polyethylene
chip. Specifically, the melting process and the extrusion process are performed, for
example, at 150 to 315°C, preferably 250 to 315°C, and still preferably 265 to 310°C.
That is, the extruder 100 and the die 200 are maintained at 150 to 315°C, preferably
250 to 315°C, and more preferably 265 to 310°C.
[0059] When a spinning temperature is lower than 150°C, the polyethylene is not uniformly
melted due to a low spinning temperature, resulting in difficulty in spinning. On
the other hand, when the spinning temperature is higher than 315°C, a desired strength
may not be exhibited due to thermal decomposition of the polyethylene.
[0060] LID that is a ratio of a hole length L to a hole diameter D of the die 200 may be
3 to 40. When LID is less than 3, a die swell phenomenon may occur during melt extrusion,
and an elastic behavior of the polyethylene is not easily controlled, resulting in
poor spinnability. When LID exceeds 40, a yarn breakage may occur due to a necking
phenomenon of the molten polyethylene passing through the die 200, and discharge unevenness
may occur due to a decrease in pressure.
[0061] The polyethylene is solidified by a difference between the spinning temperature and
room temperature while the molten polyethylene is discharged through the holes of
the die 200 to form semi-solidified filaments 11. In the present specification, both
the semi-solidified filaments and fully solidified filaments are collectively referred
to as "filaments".
[0062] A plurality of filaments 11 are cooled in a cooling zone (or a quenching zone) 300
to be fully solidified. The cooling of the filaments 11 may be performed by an air
cooling method.
[0063] In addition, multi-stage cooling is performed at the time of the cooling in the cooling
zone, such that more uniform crystallization may be obtained. Therefore, a yarn that
further smoothly discharges moisture and sweat and has an excellent cooling sensation
may be manufactured.
[0064] Subsequently, the cooled and fully solidified filaments 11 may be interlaced by an
interlacer 400 to form a multi-filament 10.
[0065] As illustrated in FIG. 1, the polyethylene yarn of the present invention may be manufactured
by a direct spinning drawing (DSD) process. That is, the multi-filament 10 may be
directly transferred to a multi-stage drawing unit 500 including a plurality of godet
rollers GR1 to GRn, the transferred multi-filament 10 may be subjected to multi-stage
drawing at a total draw ratio of 2 to 20 and preferably 3 to 15, and then, the drawn
multi-filament 10 may be wound around a winder 600. In addition, shrinkage drawing
(relaxation) of 1 to 5% is applied in the final drawing section at the time of the
multi-stage drawing, such that a yarn having more excellent durability may be provided.
[0066] Alternatively, the polyethylene yarn of the present invention may be manufactured
by winding the multi-filament 10 as an undrawn yarn and then drawing the undrawn yarn.
That is, the polyethylene yarn of the present invention may be manufactured through
a two-stage process of melt-spinning polyethylene to manufacture an undrawn yarn and
then drawing the undrawn yarn.
[0067] A functional fabric according to the present invention includes the dope dyed polyethylene
yarn. Since the functional fabric includes the dope dyed polyethylene yarn having
excellent color uniformity and an excellent thermal conductivity, such that the functional
fabric may have excellent coloring characteristics and color uniformity and may have
a cooling sensation.
[0068] The functional fabric according to the present invention may be manufactured using
the dope dyed polyethylene yarn described above alone, and may further include a yarn
different from the dope dyed polyethylene yarn in order to further impart another
functionality. It is preferable that the polyethylene yarn is used alone in terms
of having both excellent cooling sensation and color uniformity.
[0069] Specifically, the functional fabric may have a contact cooling sensation of 0.1 to
0.3 W/cm
2 when measured by bringing a heat plate (T-box) heated to 30 ± 2°C into contact with
the functional fabric at 20 ± 2°C at 20 ± 2°C and 65 ± 2% R.H, and may have a thermal
conductivity in a thickness direction of 0.05 to 0.25 W/mK when measured by bringing
a heat source plate (BT-box) heated to 30 ± 2°C into contact with the functional fabric
at 20 ± 2°C at 20 ± 2°C and 65 ± 2% R.H. More specifically, the contact cooling sensation
may be 0.15 to 0.22 W/cm
2, and the thermal conductivity may be 0.08 to 0.2 W/mK. The functional fabric having
a cooling sensation may provide an appropriate cooling sensation for a user to feel
comfortable in a high temperature environment when it is worn by the user after being
manufactured or processed into a product later.
[0070] The fabric may be processed into a product having a cooling sensation requiring an
appropriate cooling sensation. The product may be any textile product according to
the related art, and may be preferably summer clothes, sportswear, masks, and work
clothes to impart a cooling sensation to a human body.
[0071] Hereinafter, the present invention will be described in more detail with reference
to Examples. However, the following Examples are only reference examples for describing
the present invention in detail, and the present invention is not limited thereto
and may be implemented in various forms.
[0072] Unless otherwise defined, all technical terms and scientific terms used herein have
the same meanings as commonly understood by those skilled in the art to which the
present invention pertains. The terms used for the description herein are only for
effectively describing a certain Example rather than limiting the present invention.
In addition, unless otherwise stated in the specification, a unit of an additive may
be wt%.
[0073] Physical properties were measured as follows.
[Measurement of physical properties of yarn]
<1. Measurement of computer color matching (CCM)>
[0074] As illustrated in FIG. 2, a measurement region was formed by winding a dope dyed
polyethylene yarn around a substrate having a width of 6.5 cm, a length of 6.5 cm,
and a height of 0.5 cm, computer color matching (CCM) was measured in the measurement
region, and the CCM was measured every time the dope dyed polyethylene yarn was wound
around the substrate 70 turns (± 10). The total number of times of measurement of
CCM was 135.
[0075] The CCM was measured by a colorimeter (KAE1-063, GNB TECH), and L*, a*, and b* values
and a value of the following expression were calculated.

wherein C
max, C
min, and C
aver represent maximum, minimum, and average values of any one selected from L*, a*, and
b*, respectively.
<2. Weight average molecular weight (Mw) (g/mol) and polydispersity index (PDI)>
[0076] A polyethylene yarn was completely dissolved in the following solvent, and then,
a weight average molecular weight (Mw) and a polydispersity index (Mw/Mn: PDI) of
the polyethylene yarn were calculated using gel permeation chromatography (GPC).
- Analyzer: HLC-8321 GPC/HT, Tosoh Corporation
- Column: PLgel guard (7.5 × 50 mm) + 2 × PLgel mixed-B (7.5 × 300 mm)
- Column temperature: 160°C
- Solvent: trichlorobenzene (TCB) + 0.04 wt% dibutylhydroxytoluene (BHT) (after drying
with 0.1% CaCl2)
- Injector and detector temperature: 160°C
- Detector: RI detector
- Flow rate: 1.0 ml/min
- Injection amount: 300 µL
- Sample concentration: 1.5 mg/mL
- Standard sample: polystyrene
<3. Strength (g/d) and initial modulus (g/d)>
[0077] A stress-strain curve of the polyethylene yarn was obtained using a universal tensile
tester (Instron Engineering Corp., Canton, Mass) according to the ASTM D2256 method.
A sample length was 250 mm, a tensile speed was 300 mm/min, and an initial load was
set to 0.05 g/d. A strength (g/d) was calculated from a stress and an elongation at
a breaking point, and an initial modulus (g/d) was calculated from a tangent line
providing a maximum gradient on the curve in the vicinity of the origin point. The
measurement was performed 5 times for each yarn, and an average of the values was
calculated.
<4. Degree of crystallinity>
[0078] A degree of crystallinity of the polyethylene yarn was measured using an X-ray diffractometer
(XRD) [manufacturer: Malvern Panalytical, model name: EMPYREAN]. Specifically, 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 the 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°/sec
<5. Strength at break (kgf) and elongation at break (%)>
[0079] A strength at break of the yarn sample was measured by applying a tensile speed of
300 mm/min to a sample having a size of 250 mm using an Instron tester (Instron Engineering
Corp., Canton, Mass) according to the ASTM D-885 test method.
<6. Dry heat shrinkage rate>
[0080] According to the ASTM D4974-04 method, each of an initial length (L1) of the sample
in a state in which a load of 0.2 gld was applied and a length (L2) of the sample
after 2 minutes in a state in which a load of 0.2 g/d was applied at 100°C was measured
using a dry heat shrinkage rate measuring apparatus (manufacturer: TESTRITE, model
name: MK-V), and a dry heat shrinkage rate (%) of the yarn was calculated by the following
Expression 2:

<7. Melt index>
[0081] A melt index (Ml, @190°C) was measured at 190°C and 2.16 kg according to ASTM D1238.
[Measurement of physical properties of fabric]
<1. Contact cooling sensation>
[0082] Upon request, Korea Apparel Testing & Research Institute (KATRI) measured a contact
cooling sensation in a test environment of 20 ± 2°C and 65 ± 2% R.H using KES-F7 (Thermo
Labo II) apparatus.
[0083] Specifically, a fabric sample having a size of 20 cm × 20 cm was prepared, and the
fabric sample was left under conditions of a temperature of 20 ± 2°C and RH of 65
± 2% for 24 hours. Subsequently, a contact cooling sensation (Q max) of the fabric
was measured in a test environment of a temperature of 20 ± 2°C and RH of 65 ± 2%
using KES-F7 THERMO LABO II (Kato Tech Co., Ltd.) apparatus. Specifically, as illustrated
in FIG. 3, a fabric sample 23 was placed onto a base plate (also referred to as "Water-Box")
21 maintained at 20°C ± 2°C, and a heat plate (T-Box) 22a (contact area: 3 cm × 3
cm) heated to 30°C ± 2°C was placed onto the fabric sample 23 for only 1 second. That
is, one surface of the fabric sample 23 having the other surface in contact with the
base plate 21 was instantaneously brought into 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. Subsequently, a Q max value displayed on a monitor (not illustrated) connected to
the apparatus was recorded. Such a test was repeated 10 times, and an arithmetic mean
of the Q max values was calculated.
<2. Thermal conductivity>
[0084] A fabric sample having a size of 20 cm × 20 cm was prepared, and the fabric sample
was left under conditions of a temperature of 20 ± 2°C and RH of 65 ± 2% for 24 hours.
Subsequently, a thermal conductivity and a heat transfer coefficient of the fabric
were measured in a test environment of a temperature of 20 ± 2°C and RH of 65 ± 2%
using KES-F7 THERMO LABO II (Kato Tech Co., Ltd.) apparatus. Specifically, as illustrated
in FIG. 4, the fabric sample 23 was placed onto the base plate 21 maintained at 20°C
± 2°C, and a heat source plate (BT-Box) 22b (contact area: 5 cm × 5 cm) at 30°C ±
2°C was placed onto the fabric sample 23 for 1 minute. Heat was continuously supplied
to the BT-Box 22b so that the temperature of the BT-Box 22b was maintained at 30°C
± 2°C even while the BT-Box 22b was in contact with the fabric sample 23. The quantity
of heat (that is, a heat flow loss) supplied to maintain the temperature of the BT-Box
22b was displayed on a monitor (not illustrated) connected to the apparatus. Such
a test was repeated 5 times, and an arithmetic mean of the heat flow loss values was
calculated. Subsequently, a thermal conductivity and a heat transfer coefficient of
the fabric were calculated using the following Expressions 3 and 4:

wherein K is the thermal conductivity (W/cm·°C), D is a thickness (cm) of the fabric
sample 23, A is the contact area (= 25 cm
2) of the BT-Box 22b, ΔT is a temperature difference (= 10°C) between the both surfaces
of the fabric sample 23, W is the heat flow loss (Watt), and k is the heat transfer
coefficient (W/cm
2·°C).
[Example 1]
<Preparation of color masterbatch>
[0085] A first master chip was obtained by mixing a pigment with polyethylene in the form
of a chip, and then, the dried first master chip was melted and mixed again to obtain
a second master chip, that is, a color masterbatch. In this case, the pigment was
mixed in an amount of 0.83 wt% with respect to the total weight of the color masterbatch.
<Manufacturing of polyethylene yarn>
[0086] A dope dyed polyethylene yarn having a total fineness of 410 denier was manufactured.
[0087] Specifically, a polyethylene chip having a weight average molecular weight (Mw) of
154,604 g/mol and the second master chip were injected into an extruder to melt them,
thereby forming a melt. In this case, the second master chip was mixed in an amount
of 3 wt% with respect to the total weight of the melt. The melt was extruded through
a die having 200 holes. LID that was a ratio of a length L to a hole diameter D of
the die was 6. The die temperature was 270°C.
[0088] Filaments formed while being discharged through nozzle holes of the die were cooled,
interlaced, and then drawn. Subsequently, the drawn multi-filament was wound around
a winder. The winding tension was 0.8 g/d.
[0089] The physical properties of the manufactured yarn were measured. The calculated value
of (C
max - C
min)/C
aver × 100 is shown in Table 1 as a ΔC value.
<Manufacturing of functional fabric>
[0090] The manufactured dope dyed polyethylene yarn was weaved to manufacture a functional
fabric having an area density of 500 g/m
2. The physical properties of the manufactured functional fabric were measured. The
results are shown in Table 2.
[Example 2]
[0091] A yarn and a fabric were manufactured in the same manner as that of Example 1, except
that the content of the pigment in the color masterbatch was changed from 0.83 wt%
to 0.40 wt% and the content of the color masterbatch in the melt was changed from
3 wt% to 3.3 wt% in Example 1. In addition, the measured physical properties of the
yarn and the fabric manufactured in the same manner as that of Example 1 are shown
in Tables 1 and 2, respectively.
[Example 3]
[0092] A yarn and a fabric were manufactured in the same manner as that of Example 1, except
that the content of the pigment in the color masterbatch was changed from 0.83 wt%
to 0.40 wt% and the content of the color masterbatch in the melt was changed from
3 wt% to 3.8 wt% in Example 1. In addition, the measured physical properties of the
yarn and the fabric manufactured in the same manner as that of Example 1 are shown
in Tables 1 and 2, respectively.
[Comparative Example 1]
[0093] A yarn and a fabric were manufactured in the same manner as that of Example 1, except
that a pigment was mixed with polyethylene in the form of a chip having a weight average
molecular weight (Mw) of 134,277 glmol to obtain a first master chip, the dried first
master chip was used as a color masterbatch, the content in the pigment in the color
masterbatch was changed to 10.0 wt%, and the content of the color masterbatch in the
melt was changed from 3 wt% to 0.25 wt% in Example 1. In addition, the measured physical
properties of the yarn and the fabric manufactured in the same manner as that of Example
1 are shown in Tables 1 and 2, respectively.
Table 1
Classification |
Example 1 |
Example 2 |
Example 3 |
Comparativ e Example 1 |
Physical properties of polyethylene yarn |
CCM |
L* average (Caver) |
67.91 |
66.82 |
68.95 |
63.18 |
L* minimum (Cmin) |
65.30 |
65.90 |
67.18 |
58.17 |
L* maximum (Cmax) |
71.63 |
39.33 |
70.63 |
69.67 |
ΔC |
9.32 |
5.13 |
5.00 |
18.20 |
L* standard deviation |
1.26 |
0.83 |
0.66 |
3.23 |
PDI |
7.7 |
8.1 |
7.2 |
7.5 |
Mw (g/mol) |
137,267 |
139,768 |
146,822 |
134,277 |
Degree of crystallinity (%) |
75.1 |
75.6 |
74.2 |
65.2 |
Strength (g/d) |
12.5 |
13.1 |
13.4 |
7.64 |
Initial modulus (g/d) |
140.2 |
147.7 |
153.5 |
111 |
Strength at break (kgf) |
5.13 |
5.37 |
5.49 |
3.1 |
Elongation at break (%) |
8.2 |
7.8 |
7.0 |
13.8 |
Melt index (g/10 min) |
5.4 |
7.3 |
7.4 |
11.9 |
[Table 2]
Classification |
Example 1 |
Example 2 |
Example 3 |
Comparative Example 1 |
Physical properties of functional |
Contact cooling sensation (W/cm2) |
0.208 |
0.207 |
0.212 |
0.151 |
fabric |
Thermal conductivity (W/mK) |
0.105 |
0.107 |
0.112 |
0.123 |
[0094] Referring to Tables 1 and 2, in the case of the fabric according to each of Examples,
it was confirmed that the mechanical properties such as the strength and the elongation
were excellent, the cooling sensation was excellent, and the color uniformity of the
yarn was significantly excellent.
[0095] FIG. 5 illustrates the result obtained by measuring the value of the CCM over time
in the measurement region of the dope dyed polyethylene yarn illustrated in FIG. 2
while spinning the dope dyed polyethylene yarn according to each of Examples. Specifically,
the values of the CCMs of the dope dyed polyethylene yarns according to Examples 1
to 3 and Comparative Example 1 are illustrated.
[0096] Referring to FIG. 5, in the dope dyed polyethylene yarn according to the present
invention, it was confirmed that the color was hardly changed even during spinning
for a long period of time, and thus, the yarn having excellent color uniformity was
manufactured.
[0097] Hereinabove, although the present invention has been described by specific matters,
exemplary embodiments, and drawings, they have been provided only for assisting in
the entire understanding of the present invention. Therefore, the present invention
is not limited to the exemplary embodiments. Various modifications and changes may
be made by those skilled in the art to which the present invention pertains from this
description.
[0098] Therefore, the spirit of the present invention should not be limited to the described
exemplary embodiments, but the claims and all modifications equal or equivalent to
the claims are intended to fall within the scope and spirit of the present invention.
[Detailed Description of Elements]
[0099]
10: Multi-filament 11: Filament
21: Base plate 23: Fabric
22a: T-box 22b: BT-box
100: Extruder 200: Die
300: Cooling zone 400: Interlacer
500: Drawing unit 600: Winder