Patent Application
20250019869
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.
A high-density polyethylene (HDPE) yarn refers to a high-strength polyethylene yarn having a density of 0.94 g/cm3 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 ultra-high strength.
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.
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.
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.
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.
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.
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.
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.
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.
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:
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 Cmax, Cmin, and Caver represent maximum, minimum, and average values of any one selected from L*, a*, and b*, respectively.
When the CCM of the dope dyed polyethylene yarn is measured, a standard deviation of values of L* may be 3 or less.
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.
A degree of crystallinity of the dope dyed polyethylene yarn may be 60 to 80%.
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.
The dope dyed polyethylene yarn may have a melt index (MI, @190° C.) of 0.5 to 22 g/10 min when measured according to ASTM D1238.
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.
In another general aspect, a functional fabric is manufactured using the dope dyed polyethylene yarn.
The functional fabric may have a contact cooling sensation of 0.1 to 0.3 W/cm2 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.
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.
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.
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.
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.
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.
In addition, unless the context clearly indicates otherwise, the singular forms used in the present specification may be intended to include the plural forms.
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.
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.
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.
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.
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.
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:
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 Cmax, Cmin, and Caver represent maximum, minimum, and average values of any one selected from L*, a*, and b*, respectively.
Specifically, in the expression, (Cmax−Cmin)/Caver×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.
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.
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.
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.
In the measurement region formed by the method described above, when the n-1th (n is a natural number of 2 or more) CCM is measured and then the nth CCM is measured, a measurement region for measuring the nth CCM may be formed on a measurement region formed for measuring the n-1th CCM.
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.
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.
Therefore, the first measurement region in which the n-1th CCM is measured and the second measurement region in which the nth 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.
L*, a* and b* of the CCM measured in the measurement region may satisfy the expression described above.
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.
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.
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.
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.
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.
In addition, a melt index (MI, @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/cm3. 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.
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.
The dope dyed polyethylene yarn of the present invention may be manufactured by a dope dyeing method.
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 nth 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.
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.
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.
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.
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
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.
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.
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.
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.
L/D that is a ratio of a hole length L to a hole diameter D of the die 200 may be 3 to 40. When L/D 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 L/D 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.
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”.
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.
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.
Subsequently, the cooled and fully solidified filaments 11 may be interlaced by an interlacer 400 to form a multi-filament 10.
As illustrated in
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.
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.
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.
Specifically, the functional fabric may have a contact cooling sensation of 0.1 to 0.3 W/cm2 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/cm2, 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.
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.
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.
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 %.
Physical properties were measured as follows.
As illustrated in
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 Cmax, Cmin, and Caver 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)
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).
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.
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.
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.
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 g/d 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:
A melt index (MI, @190° C.) was measured at 190° C. and 2.16 kg according to ASTM D1238.
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.
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
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
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 cm2) 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/cm2·° C.).
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.
A dope dyed polyethylene yarn having a total fineness of 410 denier was manufactured.
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. L/D that was a ratio of a length L to a hole diameter D of the die was 6. The die temperature was 270° C.
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.
The physical properties of the manufactured yarn were measured. The calculated value of (Cmax−Cmin)/Caver×100 is shown in Table 1 as a ΔC value.
The manufactured dope dyed polyethylene yarn was weaved to manufacture a functional fabric having an area density of 500 g/m2. The physical properties of the manufactured functional fabric were measured. The results are shown in Table 2.
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.
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.
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 g/mol 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.
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.
Referring to
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.
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.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2021-0175078 | Dec 2021 | KR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/KR2022/019716 | 12/6/2022 | WO |
