WO2012117596A1 - 高機能ポリエチレン繊維、及び染色高機能ポリエチレン繊維 - Google Patents
高機能ポリエチレン繊維、及び染色高機能ポリエチレン繊維 Download PDFInfo
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- WO2012117596A1 WO2012117596A1 PCT/JP2011/071057 JP2011071057W WO2012117596A1 WO 2012117596 A1 WO2012117596 A1 WO 2012117596A1 JP 2011071057 W JP2011071057 W JP 2011071057W WO 2012117596 A1 WO2012117596 A1 WO 2012117596A1
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- polyethylene fiber
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- dtex
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/02—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D01F6/04—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polyolefins
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- A—HUMAN NECESSITIES
- A41—WEARING APPAREL
- A41D—OUTERWEAR; PROTECTIVE GARMENTS; ACCESSORIES
- A41D19/00—Gloves
- A41D19/015—Protective gloves
- A41D19/01505—Protective gloves resistant to mechanical aggressions, e.g. cutting. piercing
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F110/00—Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F110/02—Ethene
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D5/00—Formation of filaments, threads, or the like
- D01D5/24—Formation of filaments, threads, or the like with a hollow structure; Spinnerette packs therefor
- D01D5/247—Discontinuous hollow structure or microporous structure
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/10—Other agents for modifying properties
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F11/00—Chemical after-treatment of artificial filaments or the like during manufacture
- D01F11/04—Chemical after-treatment of artificial filaments or the like during manufacture of synthetic polymers
- D01F11/06—Chemical after-treatment of artificial filaments or the like during manufacture of synthetic polymers of macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
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- D—TEXTILES; PAPER
- D02—YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
- D02G—CRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
- D02G3/00—Yarns or threads, e.g. fancy yarns; Processes or apparatus for the production thereof, not otherwise provided for
- D02G3/22—Yarns or threads characterised by constructional features, e.g. blending, filament/fibre
- D02G3/32—Elastic yarns or threads ; Production of plied or cored yarns, one of which is elastic
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- D—TEXTILES; PAPER
- D02—YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
- D02G—CRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
- D02G3/00—Yarns or threads, e.g. fancy yarns; Processes or apparatus for the production thereof, not otherwise provided for
- D02G3/22—Yarns or threads characterised by constructional features, e.g. blending, filament/fibre
- D02G3/36—Cored or coated yarns or threads
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- D—TEXTILES; PAPER
- D02—YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
- D02G—CRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
- D02G3/00—Yarns or threads, e.g. fancy yarns; Processes or apparatus for the production thereof, not otherwise provided for
- D02G3/44—Yarns or threads characterised by the purpose for which they are designed
- D02G3/442—Cut or abrasion resistant yarns or threads
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- D—TEXTILES; PAPER
- D02—YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
- D02J—FINISHING OR DRESSING OF FILAMENTS, YARNS, THREADS, CORDS, ROPES OR THE LIKE
- D02J1/00—Modifying the structure or properties resulting from a particular structure; Modifying, retaining, or restoring the physical form or cross-sectional shape, e.g. by use of dies or squeeze rollers
- D02J1/22—Stretching or tensioning, shrinking or relaxing, e.g. by use of overfeed and underfeed apparatus, or preventing stretch
- D02J1/224—Selection or control of the temperature during stretching
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- D—TEXTILES; PAPER
- D03—WEAVING
- D03D—WOVEN FABRICS; METHODS OF WEAVING; LOOMS
- D03D15/00—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used
- D03D15/50—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the properties of the yarns or threads
- D03D15/56—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the properties of the yarns or threads elastic
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04B—KNITTING
- D04B1/00—Weft knitting processes for the production of fabrics or articles not dependent on the use of particular machines; Fabrics or articles defined by such processes
- D04B1/22—Weft knitting processes for the production of fabrics or articles not dependent on the use of particular machines; Fabrics or articles defined by such processes specially adapted for knitting goods of particular configuration
- D04B1/24—Weft knitting processes for the production of fabrics or articles not dependent on the use of particular machines; Fabrics or articles defined by such processes specially adapted for knitting goods of particular configuration wearing apparel
- D04B1/28—Weft knitting processes for the production of fabrics or articles not dependent on the use of particular machines; Fabrics or articles defined by such processes specially adapted for knitting goods of particular configuration wearing apparel gloves
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04B—KNITTING
- D04B21/00—Warp knitting processes for the production of fabrics or articles not dependent on the use of particular machines; Fabrics or articles defined by such processes
- D04B21/14—Fabrics characterised by the incorporation by knitting, in one or more thread, fleece, or fabric layers, of reinforcing, binding, or decorative threads; Fabrics incorporating small auxiliary elements, e.g. for decorative purposes
- D04B21/18—Fabrics characterised by the incorporation by knitting, in one or more thread, fleece, or fabric layers, of reinforcing, binding, or decorative threads; Fabrics incorporating small auxiliary elements, e.g. for decorative purposes incorporating elastic threads
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/165—Ethers
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/165—Ethers
- D06M13/17—Polyoxyalkyleneglycol ethers
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/53—Polyethers
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/79—Polyolefins
- D06P3/794—Polyolefins using dispersed dyes
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
- D06M2101/16—Synthetic fibres, other than mineral fibres
- D06M2101/18—Synthetic fibres consisting of macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M2101/20—Polyalkenes, polymers or copolymers of compounds with alkenyl groups bonded to aromatic groups
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- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2321/00—Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D10B2321/02—Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds polyolefins
- D10B2321/021—Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds polyolefins polyethylene
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
- Y10T428/2964—Artificial fiber or filament
- Y10T428/2967—Synthetic resin or polymer
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/30—Woven fabric [i.e., woven strand or strip material]
- Y10T442/3008—Woven fabric has an elastic quality
- Y10T442/3024—Including elastic strand or strip
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/40—Knit fabric [i.e., knit strand or strip material]
- Y10T442/413—Including an elastic strand
Definitions
- the present invention relates to a polyethylene fiber having a small change in physical properties in the region from around room temperature to around the crystal dispersion temperature of polyethylene, and excellent in dimensional stability, dyeability and cut resistance.
- high-performance textiles such as various sports clothing, bulletproof / protective clothing / protective gloves, and various safety goods; various rope products such as tag ropes, mooring ropes, yacht ropes, construction ropes; various braided products such as fishing lines and blind cables ; Net products such as fishing nets and ball-proof nets; Chemical filters, battery separators and reinforcing materials for various nonwoven fabrics; Curtain materials for tents, etc .; Reinforcing fibers for sports such as helmets and skis, composites such as speaker cones and prepregs High-strength fibers are used in a wide range of industries.
- a polyethylene fiber having a high elastic modulus produced by using a so-called gel spinning method in which ultra high molecular weight polyethylene is dissolved in a solvent has already been used (see, for example, Patent Document 1).
- the said polyethylene fiber uses an organic solvent for manufacture, there exists a problem which a working environment deteriorates at the time of this polyethylene fiber preparation.
- even in a case where the product is used indoors or outdoors even after it is made into a product even a trace amount of residual solvent remaining in the polyethylene fiber causes a burden on the environment, which is a problem.
- polyethylene fibers using a melt spinning method using high molecular weight polyethylene as a raw material have been proposed (see, for example, Patent Documents 2 and 3).
- the polyethylene fiber obtained by this means has a lower molecular weight of the polyethylene raw material used than the polyethylene fiber obtained by the gel spinning method.
- the fiber which has a high elongation and a high shrinkage rate is obtained by this means.
- the polymer molded body having such characteristics exhibits excellent performance for applications in which heat shrinkage is positively performed.
- Patent Document 4 discloses a method of forming a polyethylene microporous film. This microporous formation method is achieved by using a plasticizer and removing the plasticizer with a solvent.
- microporous formation is described as being preferably used for battery separators, diaphragms for electrolytic capacitors, various filters, moisture-permeable and waterproof clothing, etc., and is used as a so-called separation membrane. Therefore, there was no description or suggestion on improving the dyeability of polyethylene fibers.
- An object of the present invention is to solve the above-described conventional problems. Specifically, a highly functional polyethylene fiber having a high mechanical property retention rate and excellent dimensional stability not only in the product processing temperature range but also in the product use temperature range is obtained. Further, the present invention provides a high-performance polyethylene fiber that can achieve a high dye exhaustion rate by a simple dyeing operation and is excellent in dyeing fastness. This provides high-performance polyethylene fibers that can be used as various industrial materials as ropes, nets, woven and knitted fabrics, and reinforcing fibers. Another object of the present invention is to provide a method for producing the high-performance polyethylene fiber.
- fibers are produced through a melt spinning method using no solvent and a drawing step in order to avoid adverse effects on manufacturing workers and the environment. Furthermore, the heat treatment step after the stretching step, and the tension at the time of winding after the heat treatment step are precisely controlled.
- the present inventors pay attention to heat treatment conditions and winding conditions after the stretching process, mechanical thermal analysis (TMA) and thermal contraction rate of the polyethylene fiber, solid viscoelasticity, and higher-order structure of the polyethylene fiber. As a result, the present invention has been completed.
- TMA mechanical thermal analysis
- the intrinsic viscosity [ ⁇ ] is 0.8 dL / g or more and 4.9 dL / g or less
- the repeating unit is substantially ethylene
- TMA Mechanism Thermal Analysis
- the maximum shrinkage stress is 0.4 cN / dtex or less
- the thermal shrinkage rate at 100 ° C. is 2.5% or less.
- the shrinkage stress at 50 ° C. in TMA is preferably 0.05 cN / dtex or less
- the shrinkage stress at 80 ° C. is preferably 0.2 cN / dtex or less.
- the second aspect of the high-performance polyethylene fiber of the present invention is that the intrinsic viscosity [ ⁇ ] is 0.8 dL / g or more and 4.9 dL / g or less, the repeating unit is substantially ethylene, and the storage modulus at 105 ° C. is maintained. The rate is 30% or more with respect to the storage elastic modulus at 30 ° C.
- the storage elastic modulus retention at 80 ° C. is preferably 50% or more with respect to the storage elastic modulus at 30 ° C.
- the storage elastic modulus retention at 50 ° C. is 80% with respect to the storage elastic modulus at 30 ° C. The above is preferable.
- the intrinsic viscosity [ ⁇ ] is 0.8 dL / g or more and 4.9 dL / g or less
- the repeating unit is substantially ethylene
- the range is from ⁇ 50 ° C. to 60 ° C.
- the storage elastic modulus at intervals of 10 ° C. is 60% or more and 130% or less with respect to the storage elastic modulus at 20 ° C.
- the intrinsic viscosity [ ⁇ ] is 0.8 dL / g or more and 4.9 dL / g or less
- the repeating unit is substantially composed of ethylene
- the ratio of monoclinic crystals in the fiber Is 0.5% to 30%
- the ratio of orthorhombic is 40% to 90%.
- the degree of crystallinity in the fiber is preferably 60% or more and 95% or less.
- the weight average molecular weight (Mw) of polyethylene is 50,000 to 600,000, and the ratio (Mw / Mn) of the weight average molecular weight to the number average molecular weight (Mn) is 5.0 or less. It is preferable that The tensile strength is preferably 8 cN / dtex or more, and the initial elastic modulus is preferably 200 cN / dtex or more. Furthermore, the residual solvent concentration in the fiber is preferably 1000 ppm or less.
- the high-performance polyethylene fiber of the present invention has pores from the fiber surface to the inside, the pores are approximated to a cylinder, and the average diameter of the pores when measured using a mercury intrusion method with a contact angle of 140 degrees is 3 nm to It is preferable that the porosity is 1.5 to 20% at 1 ⁇ m.
- the polyethylene fiber preferably contains 0.005 to 10.0% by mass of an organic substance having an affinity for both the disperse dye and the polyethylene.
- the organic substance having an affinity for both the disperse dye and polyethylene preferably contains at least one polyether compound having a molecular weight of 500 or more.
- the high-performance polyethylene fiber of the present invention is suitable for a dyeing solution in which the disperse dye (Diaceliton fast Scarlet B (CI Disperse Red 1)) is adjusted to a concentration of 0.4 g / L and the dyeing assistant (Disper TL) is adjusted to a concentration of 1 g / L.
- the exhaustion rate when dyed at 100 ° C. for 90 minutes at a bath ratio of 1: 100 is preferably 17% or more.
- the intrinsic viscosity [ ⁇ ] is 0.8 dL / g or more and 4.9 dL / g or less, melt-spun polyethylene whose repeating unit is substantially ethylene, and further at a temperature equal to or higher than the crystal dispersion temperature of polyethylene.
- a method for producing a high-performance polyethylene fiber characterized by being subjected to a heat treatment for 0.01 seconds or more at a temperature higher by 10 ° C. or higher than the crystal dispersion temperature after stretching and then winding with a tension of 0.5 cN / dtex or less Is also included.
- the dyed high-performance polyethylene fiber of the present invention is characterized in that the high-performance polyethylene fiber is dyed with a disperse dye.
- Dyeing high-performance polyethylene fibers have a grade 3 or higher rating of washing fastness according to JIS L-0844 A-1 method and / or dry cleaning fastness according to JIS L-0860 A-1 method. Preferably there is.
- the coated elastic yarn of the present invention is characterized in that the high-performance polyethylene fiber or the dyed polyethylene fiber is covered with an elastic yarn.
- the protective woven or knitted fabric of the present invention is woven and knitted using at least a part of the high-performance polyethylene fiber, the dyed polyethylene fiber or the coated elastic yarn, and the index value of the coup tester is 2.5 or more.
- Cut-resistant gloves are suitable for the use of the protective woven or knitted fabric.
- the high-performance polyethylene fiber of the present invention has little change in physical properties and excellent dimensional stability in a wide product processing temperature range and product use temperature range. Moreover, a high dye exhaustion rate can be achieved by aqueous dyeing at 100 ° C., and the dyeing fastness is excellent. In addition, since any color dyeing can be freely selected, it is possible to provide dyed products of various colors. Rope, nets, woven and knitted fabrics using this fiber exhibit excellent performance and design as industrial materials, and can be widely applied.
- the high-performance polyethylene fiber of the present invention has an intrinsic viscosity of 0.8 dL / g or more, preferably 1.0 dL / g or more, more preferably 1.2 dL / g or more, and 4.9 dL / g or less, preferably It is 4.0 dL / g or less, More preferably, it is 2.5 dL / g or less.
- an intrinsic viscosity 0.8 dL / g or more, preferably 1.0 dL / g or more, more preferably 1.2 dL / g or more, and 4.9 dL / g or less, preferably It is 4.0 dL / g or less, More preferably, it is 2.5 dL / g or less.
- the residual solvent concentration in the fiber is preferably 1000 ppm or less, more preferably 500 ppm or less, and still more preferably 200 ppm or less.
- the residual solvent include hydrocarbon solvents such as decalin (decahydronaphthalene).
- the high-performance polyethylene fiber preferably has a maximum shrinkage temperature of 105 ° C. or higher in TMA (mechanical thermal analysis) measurement, more preferably 110 ° C. or higher, and still more preferably 115 ° C. or higher.
- TMA mechanical thermal analysis
- the maximum shrinkage stress in TMA measurement is 0.4 cN / dtex or less, More preferably, it is 0.35 cN / dtex or less, More preferably, it is 0.3 cN / dtex or less.
- the high-performance polyethylene fiber is characterized by a small difference in dimensional stability from the room temperature region to the crystal dispersion temperature region because the strain remaining at around room temperature is small. Therefore, the shrinkage stress at 50 ° C.
- the high-functional polyethylene fiber preferably has a heat shrinkage rate at 100 ° C. of 2.5% or less, more preferably 2.3% or less, and still more preferably 2.0% or less.
- the high-performance polyethylene fiber preferably has a tensile strength of 8 cN / dtex or more. By having such tensile strength, it is possible to develop applications that could not be developed with conventional polyethylene fibers obtained by a conventional melt spinning method.
- the tensile strength is more preferably 10 cN / dtex or more, and still more preferably 11 cN / dtex or more. Higher tensile strength is preferable, and the upper limit is not particularly limited. For example, it is difficult to obtain a fiber having a tensile strength of 55 cN / dtex or more by technical and industrial production by the melt spinning method.
- the highly functional polyethylene fiber of the present invention easily absorbs the energy of the blade and exhibits high cut resistance even when the tensile strength is less than 15 cN / dtex.
- the reason for this is not clear, but is thought to be due to the presence of the pore structure described later. That is, due to the presence of the pore structure, elasticity is imparted in the cross-sectional direction of the fiber, which is the traveling direction of the blade, and the energy dispersion efficiency is increased. Therefore, if the tensile strength is 8 cN / dtex or more, it is considered that the required cut resistance can be satisfied.
- the high-performance polyethylene fiber of the present invention preferably has an initial elastic modulus of 200 cN / dtex or more and 750 cN / dtex or less. If the polyethylene fiber has such an initial elastic modulus, physical properties and shape changes are less likely to occur with respect to external forces applied during product and product processing.
- the initial elastic modulus is more preferably 250 cN / dtex or more, further preferably 300 cN / dtex or more, particularly preferably 350 cN / dtex or more, more preferably 730 cN / dtex or less, still more preferably 710 cN / dtex or less.
- the high-functional polyethylene fiber has a high storage elastic modulus retention rate in a wide temperature range.
- the storage elastic modulus retention at 105 ° C. is preferably at least 30% or more with respect to the storage elastic modulus at 30 ° C., more preferably 35% or more, and further preferably 40% or more.
- the retention rate of the storage elastic modulus at 80 ° C. is preferably 50% or more with respect to the storage elastic modulus at 30 ° C., more preferably 55% or more, and further preferably 60% or more.
- Fibers with a high storage modulus retention even under dynamic loading are less affected by environmental changes even under high temperature environments such as 50 ° C. and 80 ° C. for 24 hours or more, and have good physical property retention. Show. Here, good physical property retention refers to fluctuation within a range of 100 ⁇ 5%. Further, during post-processing using hot water such as dyeing the fiber, the higher the storage modulus retention at 105 ° C., the lower the mechanical properties after post-processing.
- the change in storage elastic modulus at ⁇ 50 ° C. to 60 ° C. is small. That is, it is preferable that the storage elastic modulus at ⁇ 50 ° C. to 60 ° C. is maintained in the range of 60% to 130%, more preferably 65% to 125% with respect to the storage elastic modulus at 20 ° C. More preferably, it is 70% or more and 120% or less. Molded products with a high storage modulus retention even under dynamic loading are less affected by environmental changes even in the environment of -50 ° C to 60 ° C, and have good strength and elastic modulus over a long period of time. Indicates the physical property retention rate.
- the tensile strength and elastic modulus retention ratios are 60% to 130%, preferably 85% to 115% even when placed in an environment of 60 ° C. for 30 days continuously. For this reason, for example, in applications that are used under high tension, such as fiber reinforced plastic, concrete reinforced fiber, and ropes, and in which the environmental temperature during use is large, fluctuations in product performance due to environmental changes can be reduced. it can.
- the high-functional polyethylene fiber preferably has a monoclinic crystal ratio of 0.5% to 30%, more preferably 1.0% to 28%, and still more preferably 2. It is 0% or more and 25% or less. Furthermore, the ratio of orthorhombic crystals is preferably 40% or more and 90% or less, more preferably 45% or more and 85% or less, and still more preferably 50% or more and 80% or less.
- the monoclinic component in the internal structure can be controlled by controlling the deformation in the molten state and solid state, heat treatment conditions, and winding tension described later. It is preferable to contain a small amount. If the monoclinic component exceeds 30%, the storage modulus retention rate tends to be difficult to maintain in the range of 60% to 130%. The reason is not clear, but it seems that the crystal structure of monoclinic crystal is more unstable than that of orthorhombic crystal.
- the ratio of monoclinic crystal and orthorhombic crystal can be obtained by solid high-resolution 13 C NMR. Specifically, it was measured at room temperature using “Avance 400 wb” (manufactured by Brukerbiospin). Magnetic field strength and spin rate were measured at 9.4 T and 4 kHz, respectively. Dipolar decoupling (DD) / MAS was used as the measurement pulse. The fiber sample was cut and filled into the rotor. The DD / MAS spectrum was measured by a single pulse method (DD / MAS method) with a waiting time of 4300 seconds and a spectrum reflecting all components. Waveform separation was performed as monoclinic, orthorhombic and amorphous components from the low magnetic field side. The ratio was determined from the monoclinic, orthorhombic and amorphous components and the area ratio of each peak.
- the crystallinity of the high-performance polyethylene fiber is preferably 60% to 95%, more preferably 70% to 90%, and still more preferably 75% to 88%.
- the crystallinity is less than 60%, not only the change rate of the storage elastic modulus at -50 ° C to 60 ° C is increased, but also the fiber properties are lowered, which is not preferable.
- the degree of crystallinity exceeds 95%, the suppleness is impaired and the texture is unfavorable when processed into a glove.
- the specific gravity of the high-performance polyethylene fiber is preferably 0.880 g / cm 3 or more, more preferably 0.920 g / cm 3 or more, and still more preferably 0.930 g / cm 3 or more. Moreover, since the said high performance polyethylene fiber is comprised from polyethylene, specific gravity is less than 1.0. The specific gravity is preferably from 0.999 g / cm 3 or less, more preferably 0.995 g / cm 3 or less, more preferably 0.990 g / cm 3 or less.
- the polyethylene used in the present invention preferably has a repeating unit substantially ethylene. Further, within the range where the effects of the present invention can be obtained, not only ethylene homopolymer but also ethylene and a small amount of other monomers such as ⁇ -olefin, acrylic acid and its derivatives, methacrylic acid and its derivatives, vinylsilane and its A copolymer with a derivative or the like can be used. These may be a copolymer or a blend of an ethylene homopolymer and a copolymer, and further a homopolymer such as other ⁇ -olefin, and may have a partial cross-linking. Good.
- the intrinsic viscosity of the fiber satisfies the above range, it may be a blend of polyethylenes having different weight average molecular weights. Furthermore, as long as the intrinsic viscosity of the fibers satisfies the above range, polyethylene blends having different molecular weight distributions (Mw / Mn) may be used.
- the other monomer such as ⁇ -olefin is preferably 5.0 mol% or less, more preferably 1.0 mol% or less, in terms of monomer units. More preferably, it is 0.2 mol% or less. Of course, it may be a homopolymer of ethylene alone.
- the high-functional polyethylene fiber preferably has a weight average molecular weight in the fiber state of 50,000 to 600,000, more preferably 70,000 to 300,000, still more preferably 90,000 to 200,000. is there.
- the weight average molecular weight is less than 50,000, not only a high draw ratio cannot be obtained in the drawing step described later, but the tensile strength of the fiber obtained by rapid cooling after drawing described below is 8 cN / dtex. No more. This is presumably because the molecular weight is low, so the number of molecular ends per cross-sectional area is large and this acts as a structural defect.
- the ratio of the weight average molecular weight to the number average molecular weight is preferably 5.0 or less.
- Mw / Mn exceeds 5.0, the tension in the stretching step described later increases due to the inclusion of the high molecular weight component, and yarn breakage frequently occurs during stretching.
- the ratio (Mw / Mn) is preferably 1.2 or more, more preferably 1.5 or more, and still more preferably 1.8 or more.
- the said weight average molecular weight and number average molecular weight mean the value calculated
- the high-performance polyethylene fiber preferably has a pore structure inside the fiber in addition to the fiber surface.
- maintained inside a fiber is securable.
- the pore structure acts as a defect of the fiber and the mechanical properties are remarkably lowered.
- the dye imparted to the fiber is difficult to drop off, and further, in combination with the molecular characteristics of polyethylene, a highly functional polyethylene fiber excellent in dyeability can be obtained. .
- the high-performance polyethylene fiber has pores from the surface to the inside of the fiber. That is, there are pores on the surface and inside of the fiber (see FIGS. 1 and 2).
- FIG. 1 is an SEM photograph in which the surface of the high-performance polyethylene fiber of the present invention is magnified 50,000 times, and pores (black portions) are observed inside the ellipse.
- FIG. 2 is an SEM photograph of a cross section cut from a direction perpendicular to the fiber axis of the highly functional polyethylene fiber of the present invention. The magnification is 50,000 times.
- the high-performance polyethylene fiber preferably has pores having an average diameter of 3 nm to 1 ⁇ m. Further, when a fiber cross section obtained by cutting the high-performance polyethylene fiber perpendicularly to the direction perpendicular to the fiber axis is observed with a scanning electron microscope (SEM) at a magnification of 20,000 times, the average diameter is 3 nm to 1 ⁇ m. It is preferable to have 0.05 or more pores per 1 ⁇ m 2 .
- the average diameter of the pores is preferably 8 nm or more and 500 nm or less, more preferably 10 nm or more and 200 nm or less, and further preferably 15 nm or more and 150 nm or less.
- the dye can be prevented from being detached when the highly functional polyethylene fiber having the pores is dyed and used as a product such as a glove. Furthermore, a decrease in mechanical properties of the fiber can also be suppressed. On the other hand, by controlling the average diameter of the pores of the polyethylene fiber to 3 nm or more, the dye can easily penetrate into the fiber and the dyeability is improved.
- the dyeability is improved and the color of the colored fiber is improved.
- a more preferable number of pores is 0.1 or more per 1 ⁇ m 2 , and further preferably 0.2 or more.
- the upper limit of the number of pores is determined by the upper limit value of the porosity described later. Therefore, the upper limit of the number of pores is not limited as long as it is included in the porosity range described later.
- the upper limit of the number of pores is 10,000 per 1 ⁇ m 2.
- the number is preferably about 8000, more preferably 8000.
- the upper limit of the number of pores is preferably about 5000 per 1 ⁇ m 2 , more preferably 1000.
- the number and average diameter of the pores can be determined by a mercury intrusion method or a nitrogen adsorption method, in addition to observation by a scanning electron microscope.
- a scanning electron microscope when the cross section of the pore is an ellipse or a polygon, the distance connecting the two most distant points present on the outer periphery of the pore is taken as the diameter.
- the pore shape of the high-performance polyethylene fiber of the present invention has anisotropy, and in addition to the fiber axis direction and the direction perpendicular to the fiber axis direction, it may have a maximum diameter in a direction crossing the fiber axis obliquely. is there.
- the high-performance polyethylene fiber preferably has a porosity of 1.5% or more and 20% or less, more preferably 1.8% or more and 15% or less, and further preferably 2.0% or more and 10% or less. It is.
- the porosity means the ratio of the volume occupied by the pores in the fiber.
- the porosity greatly affects the dyeability and mechanical properties of the fiber. When the porosity is less than 1.5%, the dyeability is lowered and the color of the colored fiber is deteriorated. On the other hand, when the porosity exceeds 20%, the pores act as structural defects on the contrary due to the increase of the voids, and the mechanical properties tend to be lowered.
- the porosity can be determined by a scanning electron microscope in addition to the mercury intrusion method.
- the average diameter of the pores determined by the mercury intrusion method is preferably 3 nm or more and 1 ⁇ m or less, more preferably 8 nm or more and 500 nm or less, more preferably 10 nm, as in the case of observation with a scanning electron microscope. As mentioned above, it is 200 nm or less, More preferably, it is 15 nm or more and 150 nm or less.
- the high-functional polyethylene fiber contains an organic substance having affinity for both the disperse dye and polyethylene while having the pores inside the fiber.
- the organic substance is considered to exist in or near the pores.
- the organic matter is preferably contained in a ratio of 0.005% by mass or more and 10.0% by mass or less, more preferably 0.05% by mass or more and 8.0% by mass or less, with respect to the high-performance polyethylene fiber. More preferably, it is 0.2 mass% or more and 5.0 mass% or less. When the content of the organic substance is 0.005% by mass or more, the dye exhaustion rate tends to increase.
- content of the said organic substance in a highly functional polyethylene fiber can be calculated
- the organic material only needs to contain both a component having affinity for disperse dyes and a component having affinity for polyethylene, and may be a mixture or a single compound.
- the organic substance include a compound having high affinity for both the disperse dye and polyethylene, and a mixture of a compound having affinity for the disperse dye and a compound having affinity for polyethylene. These organic substances are preferably those having polarity.
- the component having affinity for the disperse dye is a compound capable of dissolving the disperse dye.
- it will not specifically limit if it is an organic substance which has this effect
- the dispersing agent of a disperse dye, surfactant, a polyester type compound, etc. are mentioned.
- dispersant for the disperse dye examples include polyphthalic anionic surfactants such as naphthalene sulfonic acid formaldehyde condensate, Schaefer acid / cresol / formaldehyde condensate, and lignin sulfonic acid.
- Surfactants include surfactants such as polyalkylene glycols such as polyethylene glycol, polypropylene glycol, and polybutylene glycol, copolymers thereof, polyvinyl alcohol, nonionic surfactants, anionic surfactants, and cationic surfactants. Is mentioned.
- examples include polyether surfactants such as alkylene oxide adducts or alkylene oxide adducts of polyhydric alcohols.
- component having affinity for polyethylene examples include those capable of swelling polyethylene.
- Components having an affinity for polyethylene include paraffin, ethylene glycol or polyethylene glycol polymerized with ethylene glycol, polypropylene glycol, alkylene glycol such as polybutylene glycol; low molecular weight polyethylene, polyethylene wax, partially oxidized polyethylene wax, partial Examples include alkali metal salts of oxidized polyethylene wax.
- components having high affinity for both disperse dyes and polyethylene include polyoxyethylene, polyoxypropylene, polyoxybutylene, poly (oxyethylene-oxypropylene) random copolymer or block copolymer, poly (oxy Polyethylene compounds such as (ethylene-oxybutylene) random copolymer or block copolymer, and ethylene glycol, polyethylene glycol polymerized with ethylene glycol, polypropylene glycol, and alkylene glycol such as polybutylene glycol.
- an organic substance having high affinity for both the above-mentioned disperse dye and / or polyethylene one of the above-exemplified compounds may be used alone, or two or more may be used in combination.
- polyether examples include polyoxyethylene and polyoxybutylene.
- the molecular weight of the polyether is preferably 500 or more, more preferably 1000 or more, still more preferably 2000 or more, preferably 100,000 or less, preferably 50,000 or less, more preferably 30,000 or less. When the molecular weight exceeds 100,000, it is not preferable because the viscosity increases and it becomes difficult to uniformly apply to the entire fiber.
- at least 1 type of a polyether compound is included among the compounds illustrated above.
- the high-performance polyethylene fiber having the above-described pore structure becomes a product having a high exhaustion rate by dyeing with a disperse dye. Further, the dyed high-performance polyethylene fiber dyed with a disperse dye has excellent dyeing fastness that is practical in dark colors such as blue and black. Further, when the high-performance polyethylene fiber also has an organic substance having a high affinity for both the disperse dye and polyethylene in or near the pore structure, it has a further improved exhaust rate and dyeing fastness. It will be a thing.
- the production method for obtaining the high-performance polyethylene fiber of the present invention is preferably based on the following melt spinning method.
- melt spinning which is one of the methods for producing ultra-high molecular weight polyethylene fibers using a solvent, can produce high-strength polyethylene fibers, but it is not only low in productivity but also the health of manufacturing workers using solvents. The impact on the environment of the product and the solvent remaining in the fiber has a great impact on the health of the product user.
- the above-described polyethylene is melt-extruded using an extruder or the like, and supplied to a spinning nozzle (spinneret) using a quantitative supply device and discharged.
- the melt extrusion temperature is preferably higher than the melting point of polyethylene by 10 ° C. or more (more preferably 50 ° C. or more, more preferably 80 ° C. or more).
- the inert gas supply pressure is preferably 0.001 MPa or more and 0.8 MPa or less, more preferably 0.05 MPa or more and 0.7 MPa or less, and further preferably 0.1 MPa or more and 0.5 MPa or less. .
- a filter is provided in the nozzle pack before the spinning nozzle (spinning nozzle).
- a filter having a mesh diameter of 100 ⁇ m or less.
- a more preferable mesh diameter is 50 ⁇ m or less, and further preferably 15 ⁇ m or less.
- the nozzle diameter of the spinning nozzle is 0.3 to 2.5 mm, preferably 0.5 to 1.5 mm.
- the nozzle temperature be 80 ° C. or higher (more preferably 100 ° C. or higher) higher than the melting point of polyethylene.
- the discharge amount is preferably 0.1 g / min or more.
- the discharge linear velocity is preferably 10 to 120 cm / min, more preferably 20 to 110 cm / min, and still more preferably 30 to 100 cm / min.
- the discharged yarn is cooled to 5 to 40 ° C. and then wound at 100 m / min or more.
- the molding method in the molten state after discharging. Specifically, it is preferable to deform at a magnification of 50 times or more (more preferably 100 times or more, still more preferably 150 times or more) before winding the discharge yarn. At this time, it is important that the time required for deformation is within 3 minutes (more preferably within 2 minutes, further preferably within 1 minute). If the time required for deformation exceeds 3 minutes, structural relaxation in the molten state occurs, and the monoclinic to orthorhombic ratio in the polyethylene fiber and the void structure inside the fiber cannot be obtained.
- the obtained undrawn yarn is drawn at a frequency of at least one time below the melting point of the fiber. It is recommended that stretching be performed in two or more stages. At this time, when stretching a plurality of times, it is preferable that the temperature at the time of stretching is higher as the process proceeds to the subsequent stage.
- the stretching temperature of the initial stretching (for example, the first stretching) is preferably less than the crystal dispersion temperature of polyethylene, specifically, preferably 80 ° C. or less, and more preferably 75 ° C. or less.
- the stretching temperature at the final stage of stretching is preferably not less than the crystal dispersion temperature of polyethylene and not more than the melting point of polyethylene, specifically 90 ° C. or more and less than the melting point.
- the stretching temperature is preferably higher than the crystal dispersion temperature of polyethylene and lower than the melting point of polyethylene.
- the crystal dispersion temperature of the polyethylene fiber a value obtained by the measurement method described later is used.
- the draw ratio is preferably 6 times or more, more preferably 8 times or more, still more preferably 10 times or more, and preferably 30 times or less, more preferably 25 times or less, still more preferably 20 times. It is as follows.
- the first stage draw ratio is preferably 1.05 to 4.00 times
- the second stage draw ratio is preferably It is preferably 2.5 to 15 times.
- the molding method of the unstretched molded body in a solid state it is preferable to control the molding method of the unstretched molded body in a solid state.
- the total stretching ratio in the solid state is preferably 8 times or more (more preferably 9 times or more, and further preferably 10 times or more).
- the time required for the deformation in the solid state is preferably within 5 minutes (more preferably within 4 minutes, further preferably within 3 minutes). If the time required for deformation exceeds 5 minutes, the monoclinic and orthorhombic ratio of polyethylene fibers and the pore structure inside the fibers cannot be obtained.
- the reason why the deformation time during spinning and drawing is important is estimated as follows.
- the ratio of orthorhombic and monoclinic can be kept within a predetermined range.
- the detailed mechanism is not clarified, if the deformation time is longer than 5 minutes in the stretching conditions, the orthorhombic crystal having a stable crystal structure is also subjected to deformation stress and the ratio of the orthorhombic crystal is decreased. Presumed not.
- the time required for deformation may be short, it is necessary to give a predetermined temperature to the fiber. Therefore, a time of 0.1 second or longer, preferably 1 second or longer, more preferably 10 seconds or longer is required. .
- the crystal structure in the fiber has a predetermined ratio of orthorhombic crystal and monoclinic crystal. Due to the presence of a monoclinic crystal at a certain ratio, excellent cut resistance is exhibited even when the fiber strength is 15 cN / dtex or less. Although the details are not clear, rather than the orthorhombic crystal whose crystal structure in the fiber is all stable, a certain amount of monoclinic crystal is present in the fiber, so that it can be given from the blade as a cushion. It is estimated that energy can be dispersed. However, when the ratio of monoclinic crystal increases, stable mechanical properties with respect to temperature, which is an inherently important factor, cannot be maintained, so the ratio of orthorhombic crystal and monoclinic crystal is preferable. Further, the time required for the deformation also affects the dyeability of the fibers described later, which is one of the features of the present invention. Specifically, when the time required for deformation exceeds 5 minutes, the number of pores in the fiber imparting dyeability decreases.
- the method for treating the drawn yarn after the drawing step described above is also important. Specifically, the heat treatment temperature and time in the step of heat-treating the stretched molded body that has passed through the above-described stretching step, and the winding tension and temperature in the winding step. By precisely controlling the heat treatment conditions and the winding tension, the heat shrinkage rate at 100 ° C. can be made 2.5% or less.
- the heat treatment is performed at a temperature higher than the crystal dispersion temperature of polyethylene by 10 ° C. or more (more preferably 15 ° C. or more, more preferably 20 ° C. or more) at a temperature higher than 0.01 seconds (more preferably 0.05 seconds or more). And more preferably 0.1 seconds or more).
- the upper limit of the heat treatment temperature is the melting point of polyethylene.
- the tension applied to the high-performance polyethylene fiber during heat treatment is preferably 5 cN / dtex or less, more preferably 2 cN / dtex or less, and still more preferably 1 cN / dtex or less. When heat treatment is performed at a temperature lower than 10 ° C.
- the heating method during the heat treatment is not particularly limited. Known methods such as a hot roller, a radiation panel, a steam jet, and a hot pin are recommended, but are not limited thereto.
- the three elements of the treatment temperature, the treatment time, and the treatment tension are preferably within the above ranges.
- the treatment time is shorter than the above range or the treatment temperature is lower than the above range
- the monoclinic crystal fraction in the obtained molded product is large, and the fluctuation of the storage elastic modulus due to the temperature effect increases.
- Tend when the treatment temperature is higher than the above range, or when the tension during the treatment is larger than the above range, the molded product passing through the process is easily broken or the dynamics of the obtained molded product There is a tendency that the physical properties are low or the cut-resistant performance is lowered.
- the winding tension is preferably 0.5 cN / dtex or less, more preferably 0.4 cN / dtex or less, and still more preferably 0.3 cN / dtex or less.
- the winding tension exceeds 0.5 cN / dtex, excessive residual stress is applied to the inside of the fiber.
- the thermal contraction rate at 100 ° C. exceeds 2.5%
- the maximum contraction stress in TMA exceeds 0.4 cN / dtex.
- the shrinkage stress increases in the region from the room temperature assumed as the product's use environment temperature to the vicinity of the crystal dispersion temperature of polyethylene, resulting in changes in physical properties and dimensions due to environmental changes.
- the temperature at the time of winding is preferably 5 ° C. or more (more preferably 10 ° C. or more, more preferably 20 ° C. or more) lower than the crystal dispersion temperature. If the tension is larger than the above range, or if the temperature at the time of winding is equal to or higher than the crystal dispersion temperature, residual stress is generated inside the resulting product, and dimensional changes and mechanical property fluctuations occur after commercialization. In addition, the shrinkage stress increases in the region from the room temperature assumed as the product's use environment temperature to the vicinity of the crystal dispersion temperature of polyethylene, resulting in changes in physical properties and dimensions due to environmental changes. This is not preferable because of restrictions such as the limited use temperature range of the product.
- the high-functional polyethylene fiber of the present invention imparts the above-mentioned organic substance having high affinity to both the disperse dye and polyethylene to the undrawn yarn.
- the step of imparting the organic material used in the present invention may be performed at any stage as long as it is before the stretching step, but it is desirable to carry out the unstretched yarn after discharging the raw material resin from the spinning nozzle. Further, the undrawn yarn may be transferred to the drawing step immediately after the organic matter is applied, but may be left for a certain period of time. If an organic substance is applied to the raw polyethylene resin before the melt extrusion process, the organic substance may be decomposed due to the influence of heat or shear in the extrusion process, and the organic substance may clog the filter mesh, resulting in a decrease in spinning productivity. is there.
- the method for applying the organic material is not particularly limited.
- the organic material or the organic solution may be a method of immersing undrawn yarn in a liquid organic material or an organic solution prepared by dispersing and dissolving the organic material in water or an organic solvent. And a method of applying or spraying to the undrawn yarn.
- the dyed high-performance polyethylene fiber of the present invention is obtained by dyeing the high-performance polyethylene fiber with a disperse dye.
- the high-performance polyethylene fiber has a bath ratio with respect to a dyeing solution in which the disperse dye (Diaceliton fast Scarlet B (CI Disperse Red1)) is adjusted to a concentration of 0.4 g / L and the dyeing assistant (Disper TL) is adjusted to a concentration of 1 g / L.
- the exhaustion rate when dyed for 90 minutes at 100 ° C. (115 ° C. oil as a heat source) at 1: 100 is preferably 17% or more.
- the exhaustion rate is more preferably 20% or more, still more preferably 22% or more, and still more preferably 30% or more.
- the exhaustion rate is determined by measuring the absorbance of the staining solution before and after staining.
- wash fastness JIS L-0844 No. A-1
- dry cleaning fastness JIS L-0860 method A-1, perchlorethylene
- a dyed high-performance polyethylene fiber having a degree of JIS L-0860 (A-1 method, perchlorethylene) having a grade of 3 or higher is obtained.
- a dyed product having equivalent dyeing fastness can also be easily obtained.
- the method for dyeing the high-performance polyethylene fiber is not particularly limited, and any conventionally known dyeing method can be employed.
- a disperse dye is preferably used. Disperse dyes hold one or more chromophores. Specific examples of the disperse dye include azo dyes, anthraquinone dyes, quinophthalone dyes, naphthalimide dyes, naphthoquinone dyes, and nitro dyes.
- disperse dyes available on the market include C.I. I. Disperse Yellow 3, C.I. I. Disperse Yellow 5, C.I. I. Disperse Yellow 64, C.I. I. Disperse Yellow 160, C.I. I. Disperse Yellow 211, C.I. I. Disperse Yellow 241, C.I. I. Disperse Orange 29, C.I. I. Disperse Orange 44, C.I. I. Disperse Orange 56, C.I. I. Disperse Red 60, C.I. I. Disperse Red 72, C.I. I. Disperse Red 82, C.I. I. Disperse Red 388, C.I. I. Disperse Blue 79, C.I. I. Disperse Blue 165, C.I. I. Disperse Blue 366, C.I. I. Disperse Blue 148, C.I. I. Dispers Violet 28, C.I. I. Disperse Green 9 is an example.
- disperse dye can be selected from an appropriate database (for example, “color index”). Details of disperse dyes and other examples are described in “Industrial dyes”, edited by Klaus Hungel, Wiley-VCH, Weinheim, 2003, pages 134-158. Therefore, what is necessary is just to select with reference to these. Two or more disperse dyes may be used in combination.
- additives such as sequestering agents and reduction inhibitors may be used. These additives may be used together with the disperse dye at the time of dyeing to give the high-performance polyethylene fiber.
- the reason why the dyed high-performance polyethylene fiber is obtained is not clear, but the present inventors presume that it is due to the following mechanism. That is, the presence of organic matter having a high affinity for both the fine pores expressed in the fiber and the disperse dye and the polyethylene fiber filled in the fiber allows the dye to penetrate into the fiber, and the above-mentioned pore structure Therefore, it is considered that the loss of the dye after commercialization can be reduced to the utmost limit.
- the use of the high-performance polyethylene fiber and / or dyed high-performance polyethylene fiber is not particularly limited.
- the high-performance polyethylene fiber may be used as a thread, or a coated elastic thread in which the elastic fiber is a core thread and the polyethylene fiber of the present invention is a sheath thread. It is preferable to make a woven or knitted fabric using this coated elastic yarn.
- the coated elastic yarn By using the coated elastic yarn, the wearing feeling of the woven or knitted fabric is enhanced, and the desorption is facilitated.
- the pores (microvoids) present on the surface and inside of the high-performance polyethylene fiber used for the sheath yarn absorb and reflect light, thereby suppressing the embrittlement of the elastic fiber (core yarn).
- Examples of the elastic fiber that can be used for the core yarn of the coated elastic yarn include, but are not particularly limited to, polyurethane-based, polyolefin-based, and polyester-based fibers.
- the elastic fiber here refers to a fiber having a recoverability of 50% or more when stretched by 50%.
- a covering machine may be used, or the elastic fiber may be twisted with the non-elastic fiber while drafting the elastic fiber.
- the mixing ratio of the elastic fibers is 1% or more, preferably 5% or more, and more preferably 10% or more by mass ratio. When the mixing ratio of elastic fibers is low, sufficient stretch recovery properties cannot be obtained. However, if the mixing ratio of the elastic fibers is too high, the strength becomes low, so 50% or less, more preferably 30% or less is preferable.
- a woven fabric or knitted fabric (woven or knitted fabric) using the coated elastic yarn is suitably used as a protective woven or knitted fabric.
- the index value of the coup tester is 2.5 or more, preferably 2.8 or more, more preferably 3.0 or more, and further preferably 4.0 from the viewpoint of durability of cut resistance. Above, especially preferably 5.0 or more.
- the fiber can be thickened to increase the index value of the coup tester. However, when the fibers are thick, the texture tends to be poor. Therefore, the index value of the coup tester is preferably 14 or less, more preferably 12 or less, and still more preferably 10 or less.
- the woven or knitted fabric using the coated elastic yarn of the present invention preferably contains 30% or more of the coated elastic yarn by mass ratio among the yarns constituting the woven or knitted fabric.
- the coated elastic yarn preferably has a single yarn fineness of 1.5 dtex or more and 220 dtex or less. Synthetic fibers such as polyester, nylon and acrylic, natural fibers such as cotton and wool, regenerated fibers such as rayon, etc.
- the index value of the woven / knitted coup tester can be within the above range.
- Protective woven or knitted fabric using the coated elastic yarn of the present invention is suitably used as a raw material for cut resistant gloves.
- the glove of the present invention can be obtained by applying the fiber and / or coated elastic yarn of the present invention to a knitting machine.
- the fabric and / or coated elastic yarn of the present invention can be applied to a loom to obtain a fabric, which can be cut and sewn to form a glove.
- the body fabric of the protective woven or knitted fabric of the present invention includes the above-described coated elastic yarn as a constituent fiber from the viewpoint of cut resistance, and the mass ratio thereof is preferably 30% or more, more preferably 50%. As mentioned above, More preferably, it is 70% or more.
- the single yarn fineness of the coated elastic yarn is preferably 1.5 dtex or more and 220 dtex or less. More preferably, it is 10 dtex or more and 165 dtex or less, More preferably, it is 20 dtex or more and 110 dtex or less.
- synthetic fibers such as polyester, nylon and acrylic, natural fibers such as cotton and wool, and regenerated fibers such as rayon may be used. From the viewpoint of ensuring friction durability, it is preferable to use a polyester multifilament having a single yarn fineness of 1 to 4 dtex or the same nylon filament.
- the woven or knitted fabric thus obtained can be used as a glove as it is, for example, but if necessary, a resin can be applied to impart anti-slip properties.
- a resin can be applied to impart anti-slip properties.
- the resin used here include urethane-based and ethylene-based resins, but are not particularly limited.
- the high-performance polyethylene fiber and / or dyed high-performance polyethylene fiber of the present invention is for tapes, ropes, safety ropes, nets, ball-proof nets, fishnet nets, fishing lines, meat fastening threads, material protective covers, sheets, and kites. It is suitably used as a thread, a bowstring, a sail cloth, and a curtain material.
- the above uses may require various colors or design properties depending on the purpose as well as mechanical properties.
- post-processing see, for example, Japanese Patent No. 4041761 for coating a resin containing an inorganic pigment or an organic pigment has often been applied, but by using the dyed high-performance polyethylene fiber of the present invention, It becomes possible to use without impairing the texture of the.
- the high-performance polyethylene fiber of the present invention has little change in physical properties over a wide temperature range and is excellent in dimensional stability. Therefore, fiber-reinforced resin reinforcement, cement reinforcement, and fiber reinforcement that require heating in the post-processing step. It is preferably used as a rubber reinforcing material, or a protective material, bulletproof material, medical suture, artificial tendon, artificial muscle, machine tool component, battery separator, or chemical filter whose environmental change is assumed.
- Intrinsic viscosity The specific viscosity of various dilute solutions was measured using an Ubbelohde capillary viscosity tube with decalin at a temperature of 135 ° C. The intrinsic viscosity was determined from the extrapolation point to the origin of the straight line obtained by the least square approximation from the plot with respect to the concentration of the diluted solution viscosity. Upon measurement, the sample was divided or cut into a length of about 5 mm, and 1% by mass of antioxidant (“Yoshinox (registered trademark) BHT” manufactured by Yoshitomi Pharmaceutical) was added to the polymer, and the temperature was 135 ° C. The measurement solution was prepared by stirring and dissolving for 4 hours.
- Weight average molecular weight Mw, number average molecular weight Mn, and Mw / Mn The weight average molecular weight Mw, the number average molecular weight Mn, and Mw / Mn were measured by gel permeation chromatography (GPC).
- GPC 150C ALC / GPC manufactured by Waters
- the column one “GPC UT802.5” (manufactured by SHODEX) and two “UT806M” (manufactured by SHODEX) are used, and the detector.
- RI detector differential refractometer
- the measurement solvent was o-dichlorobenzene, and the column temperature was 145 ° C.
- the calibration curve of molecular weight is created using a polystyrene sample with a known molecular weight by the universal calibration method.
- a cross-section sample of the fiber was prepared by the following procedure.
- a sample embedded with an acrylic resin (BUEHLER, “SAMPL-KWICK 473”) was used to measure the fiber axis at an acceleration voltage of 5 kV using a cross-section sample preparation device (JEOL, “Cross Section Polisher (registered trademark)”). The orthogonal direction was cut vertically.
- JEOL Cross-section sample preparation device
- S4800 scanning electron microscope
- Hitachi High-Technologies Corporation the cross section of the sample was observed at an acceleration voltage of 0.5 kV, and a photograph was taken at an enlargement magnification of 20,000 times.
- pores having a diameter of 3 nm to 1 ⁇ m per 1 ⁇ m 2 of an arbitrary cross section of the fiber were visually counted. This measurement was performed five times at different locations, and the average value was used. As the diameter of the pore, the maximum diameter was used when it was not circular.
- Porosity (%) 100 ⁇ (volume [mL] by pores having a diameter of 3 nm to 1 ⁇ m ⁇ sample mass [g]) / (cell volume ⁇ (mass mass [g] / (mercury density [g / mL] ]))
- the residual liquid of the dyeing liquid is returned to room temperature, 5 mL of the residual liquid and 5 mL of acetone are mixed in a measuring flask, and further acetone / water (1/1) is added to make a total of 100 ml (a). .
- 5 ml of the stock solution of the dyeing solution before use for dyeing and 5 mL of acetone were placed in a volumetric flask and mixed, and further acetone / water (1/1) was added to make a total of 100 ml (b).
- the absorbance of the residual liquid (a) and the stock solution (b) at a wavelength of 350 nm to 700 nm was measured using an ultraviolet spectrophotometer (manufactured by Hitachi, Ltd., “double beam spectrophotometric type 150-20 type”). The maximum values were defined as the absorbance a of the residual liquid and the absorbance b of the stock solution, respectively.
- the exhaustion rate (DY%) was calculated
- equation using the obtained light absorbency. DY (%) (1 ⁇ (absorbance a of residual liquid) / (absorbance b of stock solution)) ⁇ 100
- the measurement conditions were: 1H resonance frequency: 500.1 MHz, detection pulse flip angle: 45 °, data capture time: 4.0 seconds, delay time: 1.0 second, integration number: 64 times, measurement temperature: 110 The temperature was set to 0 ° C., and “TOPSPIN ver. 2.1” (manufactured by Bruker BioSpin) was used as a measurement and analysis program. Further, the sample was dissolved in heavy water, or the dry residue was dissolved in CDCl 3 , H-NMR measurement was performed, and the organic substance was quantitatively evaluated. The calculation method is as follows: The organic substance ratio (X mass%) is 0.8 to 1.5 ppm of polyethylene peak integral value A, and the organic substance peak integral value B is B / A. Obtainable.
- TMA Mechanical thermal analysis
- a thermal stress strain measuring device manufactured by Seiko Instruments Inc., “TMA / SS120C” was used.
- An initial load of 0.01764 cN / dtex was applied to a fiber sample having a length of 20 mm, the temperature was raised at a rate of temperature rise of 20 ° C./min, and the maximum shrinkage temperature and the maximum shrinkage stress were measured at 50 ° C. and 80 ° C.
- the measurement start temperature was ⁇ 10 ° C.
- the measurement end temperature was 140 ° C.
- the rate of temperature increase was 1.0 ° C./min.
- the strain amount was 0.04%
- the initial load at the start of measurement was 0.05 cN / dtex.
- the measurement frequency was 11 Hz.
- “TA Universal Analysis” manufactured by TA Instruments was used. At this time, the retention rate was calculated from the following equation.
- Storage modulus of storage modulus at 105 ° C., 80 ° C., and 50 ° C. (%) 100 ⁇ [(Storage modulus at each temperature of 105 ° C., 80 ° C., and 50 ° C.) / (Storage modulus at 30 ° C.]]
- Retention rate of storage elastic modulus at ⁇ 50 ° C. to 60 ° C. with respect to storage elastic modulus of 20 ° C. (Production Examples 17 to 31)
- a solid viscoelasticity measuring apparatus (TA Instruments, “DMA Q800”) was used. Measurement conditions were used by adjusting the measurement sample length to 10 mm and the sample fineness to about 100 dtex.
- both ends of the measurement sample were sandwiched with cardboard using an adhesive and a double-sided tape so that slippage between the fiber sample and the apparatus chuck and single yarn separation would not occur.
- the presence of cardboard between the measurement sample and the apparatus chuck in the measurement makes it possible to suppress slippage at the apparatus chuck and single yarn scattering in the case of fibers.
- the measurement start temperature was ⁇ 140 ° C.
- the measurement end temperature was 140 ° C.
- the rate of temperature increase was 1.0 ° C./min.
- the strain amount was 0.04%
- the initial load at the start of measurement was 0.05 cN / dtex.
- the measurement frequency was 11 Hz.
- “TA Universal Analysis” manufactured by TA Instruments
- a solid viscoelasticity measurement apparatus (“DMA Q800” manufactured by TA Instruments Inc.) is used for measurement, and “TA Universal Analysis” (for analysis of data) ( TA Instruments, Inc.) was used.
- the measurement was performed in the temperature range of ⁇ 140 ° C. to 140 ° C., and the rate of temperature increase was about 1.0 ° C./min.
- the strain amount was 0.04%, and the initial load at the start of measurement was 0.05 cN / dtex.
- Residual solvent concentration Gas chromatography (manufactured by Shimadzu Corporation) was used to measure the residual solvent concentration in the fiber sample. 10 mg of the sample fiber was set in a glass insert at the gas chromatography inlet. The inlet was heated above the boiling point of the solvent, and the solvent volatilized by heating was introduced into the column by nitrogen purge. The column temperature was set to 40 ° C. and the solvent was trapped for 5 minutes. Next, measurement was started after the column temperature was raised to 80 ° C. From the obtained peak, the residual solvent concentration was determined.
- Cut Resistance The cut resistance was evaluated by using a cutting tester (“SOOPMAT”, “Coop Tester”). An aluminum foil was provided on the sample stage of this apparatus, and the sample was placed thereon. Next, the circular blade provided in the apparatus was run on the sample while rotating in the direction opposite to the running direction. When the sample is cut, the circular blade and the aluminum foil come into contact with each other to energize, and sense that the cut resistance test has been completed. During the operation of the circular blade, the counter attached to the device counts the numerical value linked to the rotational speed of the circular blade, and the numerical value was recorded.
- the evaluation value calculated here is called an index and is calculated by the following equation.
- A (count value of cotton cloth before sample test + count value of cotton cloth after sample test) / 2
- Index value (sample count value + A) / A
- Dyeing method A knitted fabric was obtained using various fibers to be evaluated, and after refining the knitted fabric, a dyed knitted fabric was obtained by the steps of dyeing, reduction washing and drying, and the dyeing fastness was evaluated.
- Crystal component ratio measurement The crystal component ratio was determined by solid-state high-resolution 13 C NMR. Specifically, it was measured at room temperature using “Avance 400 wb” (manufactured by Brukerbiospin). Magnetic field strength and spin rate were measured at 9.4 T and 4 kHz, respectively. Dipolar decoupling (DD) / MAS was used as the measurement pulse. The sample was cut into strips and filled into the rotor. The DD / MAS spectrum was measured by a single pulse method (DD / MAS method) with a waiting time of 4300 seconds and a spectrum reflecting all components. Waveform separation was performed as monoclinic, orthorhombic and amorphous components from the low magnetic field side. The ratio was determined from the monoclinic, orthorhombic and amorphous components and the area ratio of each peak.
- a high density polyethylene pellet having an intrinsic viscosity of 1.9 dL / g, a weight average molecular weight of 120,000, and a ratio of the weight average molecular weight to the number average molecular weight of 2.7 is supplied to a container supplying nitrogen gas at a pressure of 0.005 MPa. Filled.
- the pellets are supplied to an extruder and melted at 280 ° C., the nozzle filter mesh diameter is 10 ⁇ m, the orifice diameter (nozzle diameter) is 0.8 mm, and the nozzle surface temperature is 280 ° C. and the single hole discharge amount is 0 It discharged at 4 g / min.
- the discharged yarn is passed through a 10 cm heat insulation section, and then cooled with a quench air with a wind speed of 0.5 m / sec in a 40 ° C. environment, and then wound into a cheese shape at a spinning speed of 270 m / min to obtain an undrawn yarn. It was.
- the drawn yarn was subjected to heat treatment at 120 ° C. for 0.2 seconds, and then wound at 25 ° C. with a tension of 0.22 cN / dtex to obtain a fiber.
- Table 1 shows the physical properties of the obtained fibers, the physical property retention after the acceleration test, TMA (mechanical thermal analysis), the storage elastic modulus retention, and the organic content.
- the obtained fiber was used as a sheath yarn, and 155 dtex spandex (manufactured by Toyobo Co., Ltd., “Espa (registered trademark))) was used as a core yarn, thereby forming a single covering yarn.
- a knitted fabric having a basis weight of 500 g / m 2 was produced with a knitting machine (manufactured by Shima Seiki Seisakusho).
- Table 1 shows index values of the obtained knitted coup tester.
- Production Example 2 A fiber, a knitted fabric, and a dyed knitted fabric were obtained in the same manner as in Production Example 1 except that the heat treatment was performed at 110 ° C. for 0.2 seconds in Production Example 1.
- Table 1 shows the physical properties of the obtained fibers, the physical property retention after the acceleration test, TMA (mechanical thermal analysis), the storage elastic modulus retention, the organic content, and the index value of the knitted fabric. It is shown in Table 3.
- Production Example 3 A fiber, a knitted fabric, and a dyed knitted fabric were obtained in the same manner as in Production Example 1 except that the heat treatment was performed at 110 ° C. for 0.012 seconds in Production Example 1.
- Table 1 shows the mechanical properties of the obtained fibers, the physical property retention after the acceleration test, TMA (mechanical thermal analysis), the storage elastic modulus retention, the organic content, and the knitted index value. Are shown in Table 3.
- Production Example 4 A fiber, a knitted fabric, and a dyed knitted fabric were obtained in the same manner as in Production Example 1 except that the winding tension in Production Example 1 was 0.41 cN / dtex.
- Table 1 shows the mechanical properties of the obtained fibers, the physical property retention after the acceleration test, TMA (mechanical thermal analysis), the storage elastic modulus retention, the organic content, and the knitted index value. Are shown in Table 3.
- Production Example 5 an undrawn yarn was obtained in the same manner as in Production Example 1, except that the cheese shape was scraped off at a spinning speed of 330 m / min.
- the obtained undrawn yarn was heated with hot air at 105 ° C. and drawn 10 times, and then subjected to a heat treatment at 120 ° C. for 0.2 seconds, followed by 0.2 ° C. at 25 ° C.
- the fiber was obtained by winding with a tension of 22 cN / dtex.
- a knitted fabric and a dyed knitted fabric were obtained in the same manner as in Production Example 1.
- Table 1 shows the physical properties of the obtained fibers, the physical property retention after the acceleration test, TMA (mechanical thermal analysis), the storage elastic modulus retention, the organic content, and the index value of the knitted fabric. It is shown in Table 3.
- Production Example 8 A fiber, a knitted fabric and a dyed knitted fabric were obtained in the same manner as in Production Example 1 except that the heat treatment at 105 ° C. for 0.5 seconds and the winding tension at 0.28 cN / dtex were used in Production Example 1.
- Table 1 shows the physical properties of the obtained fibers, the physical property retention after the acceleration test, TMA (mechanical thermal analysis), the storage elastic modulus retention, the organic content, and the index value of the knitted fabric. It is shown in Table 3.
- Table 2 shows the physical properties of the obtained fibers, the physical property retention after the acceleration test, TMA (mechanical thermal analysis), the storage elastic modulus retention, the organic content, and the knitted index value. It was found that the fibers obtained without the heat treatment had low physical property retention, high heat shrinkage rates and high shrinkage stresses of TMA, and poor dimensional stability.
- Production Example 10 A fiber was obtained in the same manner as in Production Example 9 except that a heat treatment at 60 ° C. for 0.2 seconds was performed in Production Example 9.
- Table 2 shows the physical properties of the obtained fibers, the physical property retention after the acceleration test, TMA (mechanical thermal analysis), the storage elastic modulus retention, the organic content, and the knitted index value.
- the obtained fiber had a low physical property retention rate, a high thermal shrinkage rate and a high shrinkage stress of TMA, and poor dimensional stability. It was found that the heat treatment was insufficient and the residual stress inside the fiber was not completely removed.
- Production Example 11 A fiber was obtained in the same manner as in Production Example 9 except that a heat treatment at 120 ° C. for 0.005 seconds was performed in Production Example 9.
- Table 2 shows the physical properties of the obtained fibers, the physical property retention after the acceleration test, TMA (mechanical thermal analysis), the storage elastic modulus retention, the organic content, and the knitted index value.
- the obtained fiber had a low physical property retention rate, a high thermal shrinkage rate and a high shrinkage stress of TMA, and poor dimensional stability. It was found that the heat treatment was insufficient and the residual stress inside the fiber was not completely removed.
- Production Example 12 A fiber was obtained in the same manner as in Production Example 9 except that the heat treatment at 120 ° C. for 0.2 seconds was performed in Production Example 9 to obtain a winding tension of 0.55 cN / dtex.
- Table 2 shows the physical properties of the obtained fibers, the physical property retention after the acceleration test, TMA (mechanical thermal analysis), the storage elastic modulus retention, the organic content, and the knitted index value.
- the obtained fiber had a low physical property retention rate, a high thermal shrinkage rate and a high shrinkage stress of TMA, and poor dimensional stability. It was found that stress was applied inside the fiber due to the high winding tension after the heat treatment.
- the nozzle filter mesh diameter is set to 200 ⁇ m, the diameter is set to 170 ° C., the diameter is 0.2 mm, and the metering pump is provided with a 390 hole At a single hole discharge rate of 1.0 g / min.
- Nitrogen gas adjusted to 100 ° C. is supplied at a speed of 1.2 m / min with a gas supply orifice on the slit installed immediately below the nozzle so that it strikes the yarn as evenly as possible, and decahydronaphthalene on the fiber surface is applied. Evaporated actively. Then, it cooled substantially with the airflow set to 30 degreeC, and it picked up with the speed
- the solvent contained in the form of yarn was reduced to about half of the original mass.
- the fiber was stretched 3 times in a heating oven at 120 ° C.
- This fiber was stretched 4.0 times in a heating oven set at 149 ° C.
- the film was wound up at 1 cN / dtex at 25 ° C. without going through a heat treatment step.
- Table 2 shows the physical properties of the obtained fiber, the physical property retention after the acceleration test, TMA (mechanical thermal analysis), the storage elastic modulus retention, the organic content, and the knitted index value.
- the physical property retention rate, thermal shrinkage rate, shrinkage stress, and storage modulus retention rate after the acceleration test showed very good values, but the residual solvent showed a high value of 500 ppm. Further, no pores were confirmed in the fiber, and the porosity and exhaustion rate were very low. Further, an attempt was made to produce a dyed knitted fabric in the same manner as in Production Example 1, but the test was stopped because the dyeing could not be performed to the extent that the color fastness was tested.
- a high density polyethylene pellet having an intrinsic viscosity of 0.7 dL / g, a weight average molecular weight of 42,000, and a ratio of the weight average molecular weight to the number average molecular weight of 5.1 is supplied to a container supplying nitrogen gas at a pressure of 0.005 MPa. Filled. Pellets were supplied to an extruder and melted at 230 ° C., and discharged from a spinneret consisting of a nozzle filter orifice diameter ⁇ 0.8 mm having a mesh diameter of 10 ⁇ m and 360 H at a nozzle surface temperature of 230 ° C. and a single hole discharge rate of 0.4 g / min. .
- the obtained undrawn yarn was allowed to stand for 1 day, then 1.2 times between two driving rolls set at 65 ° C. roller temperature and atmospheric temperature, and then 5.0 times heated with hot air at 100 ° C.
- the drawn yarn was continuously subjected to heat treatment at 120 ° C. for 0.2 seconds and then wound at 25 ° C. with a tension of 0.22 cN / dtex to obtain a fiber.
- Table 2 shows the physical properties of the obtained fiber, the physical property retention after the acceleration test, TMA (mechanical thermal analysis), the storage elastic modulus retention, the organic content, and the knitted index value.
- the obtained fiber had low mechanical properties and low physical property retention. Also, the index value of the knitted fabric was low. Further, the fibers had small pores, and the porosity and exhaustion rate were very low. Further, an attempt was made to produce a dyed knitted fabric in the same manner as in Production Example 1, but the test was stopped because the dyeing could not be performed to the extent that the color fastness was tested.
- a high density polyethylene pellet having an intrinsic viscosity of 1.9 dL / g, a weight average molecular weight of 120,000, and a ratio of the weight average molecular weight to the number average molecular weight of 2.7 is supplied to a container supplying nitrogen gas at a pressure of 0.005 MPa. Filled. Pellets are supplied to an extruder and melted at 280 ° C., the nozzle filter mesh diameter is 10 ⁇ m, and the nozzle diameter is 280 ° C. and the single-hole discharge rate is 0.4 g / min from the spinneret consisting of an orifice diameter of 0.8 mm and 360H. Was discharged.
- the discharged yarn is passed through a 10 cm heat insulation section, and then cooled with a quench air with a wind speed of 0.5 m / sec in a 40 ° C. environment, and then wound into a cheese shape at a spinning speed of 270 m / min to obtain an undrawn yarn. It was.
- the obtained fiber was used as a sheath yarn, and 155 dtex spandex (manufactured by Toyobo Co., Ltd., “Espa”) was used as the core yarn to obtain a single covering yarn.
- a knitted fabric having a basis weight of 500 g / m 2 was produced with a knitting machine (manufactured by Shima Seiki Seisakusho).
- Table 4 shows index values of the obtained knitted coup tester.
- Production Example 18 A fiber, a knitted fabric, and a dyed knitted fabric were obtained in the same manner as in Production Example 17 except that heat treatment was performed at 110 ° C. for 0.2 seconds in Production Example 17. The evaluation results of the obtained fibers and knitted fabrics are shown in Table 4, and the results of dyeing fastness are shown in Table 6.
- Production Example 19 A fiber, a knitted fabric, and a dyed knitted fabric were obtained in the same manner as in Production Example 17 except that the heat treatment was performed at 110 ° C. for 0.012 seconds in Production Example 17.
- Table 4 shows the evaluation results of the obtained fibers and knitted fabrics, and Table 6 shows the results of dyeing fastness.
- Table 1 shows the physical properties, storage elastic modulus retention, and mechanical properties retention of the obtained fibers.
- the obtained fiber had a low storage elastic modulus retention rate and a low physical property retention rate. Long stretch deformation time and insufficient heat treatment, so monoclinic crystal ratio is high and orthorhombic crystal ratio is low. .
- Production Example 24 A fiber was obtained in the same manner as in Production Example 23 except that a heat treatment at 60 ° C. for 0.2 seconds was performed in Production Example 23.
- Table 5 shows the physical properties, storage elastic modulus retention, and mechanical properties retention of the obtained fibers.
- the obtained fiber had a low storage elastic modulus retention rate and a low physical property retention rate. This is considered to be due to the fact that the residual stress inside the fiber is not completely removed due to the long drawing deformation time and insufficient heat treatment.
- Production Example 25 A fiber was obtained in the same manner as in Production Example 23 except that a heat treatment at 120 ° C. for 0.005 seconds was performed in Production Example 23.
- Table 5 shows the physical properties, storage elastic modulus retention, and mechanical properties retention of the obtained fibers.
- the obtained fiber had a low storage elastic modulus retention rate and a low physical property retention rate. This is considered to be due to the fact that the residual stress inside the fiber is not completely removed due to the long drawing deformation time and insufficient heat treatment.
- Example 26 A fiber was obtained in the same manner as in Production Example 23, except that in Example 23, a heat treatment was performed at a spinning deformation time of 3.3 min, 120 ° C., and 0.2 seconds to obtain a winding tension of 0.55 cN / dtex.
- Table 5 shows the physical properties, storage elastic modulus retention, and mechanical properties retention of the obtained fibers.
- the obtained fiber had a low storage elastic modulus retention rate and a low physical property retention rate. It was found that stress was applied inside the fiber due to the high winding tension after the heat treatment.
- Nitrogen gas adjusted to 100 ° C. is supplied at a speed of 1.2 m / min with a gas supply orifice on the slit installed immediately below the nozzle so that it strikes the yarn as evenly as possible, and decahydronaphthalene on the fiber surface is applied. Evaporated actively. Then, it cooled substantially with the airflow set to 30 degreeC, and it picked up with the speed
- the film was wound up at 1 cN / dtex at 25 ° C. without going through a heat treatment step. At this time, the spinning deformation time was 0.5 min and the stretching deformation time was 2.2 min. Table 5 shows the physical properties, storage elastic modulus retention, and mechanical properties retention of the obtained fibers. The residual solvent showed a high value of 1200 ppm.
- a high density polyethylene pellet having an intrinsic viscosity of 0.7 dL / g, a weight average molecular weight of 42,000, and a ratio of the weight average molecular weight to the number average molecular weight of 5.1 is supplied to a container supplying nitrogen gas at a pressure of 0.005 MPa. Filled. The pellets were supplied to an extruder, melted at 230 ° C., and discharged from a spinneret having an orifice diameter of ⁇ 0.8 mm and 360H at a nozzle surface temperature of 230 ° C. and a single hole discharge rate of 0.4 g / min.
- the discharged yarn was passed through a 10 cm heat insulation section, then cooled with a quench air at 40 ° C. and a wind speed of 0.5 m / sec, and then wound into a cheese shape at a spinning speed of 270 m / min to obtain an undrawn yarn.
- the obtained unstretched yarn was stretched 2.0 times between two drive rolls set at a roller temperature and an atmospheric temperature of 65 ° C, and then heated with hot air at 100 ° C to 4.0 times, and then stretched.
- Fibers were obtained in the same manner as in Production Example 23 except that the drawn yarn was continuously subjected to heat treatment at 120 ° C. for 0.2 seconds and then wound at 25 ° C. with a tension of 0.22 cN / dtex.
- Table 5 shows the maximum change in physical properties and storage elastic modulus of the obtained fiber.
- the obtained fiber had low mechanical properties, and the retention rate of storage elastic modulus and the retention rate of mechanical properties were significantly reduced.
- the high-performance polyethylene fiber of the present invention has little change in physical properties and can improve dimensional stability in a wide product processing temperature range and a wide use temperature range as a product. Further, the high-performance polyethylene fiber of the present invention can be dyed and the color can be freely selected.
- a protective woven or knitted fabric utilizing the cut resistance characteristic of the fiber, or the fiber alone or dyed polyethylene fiber as a tape, rope, net, fishing line, material protective cover, sheet, kite thread, bow bow , Sail cloth, curtain material, protective material, bulletproof material, medical suture, artificial tendon, artificial muscle, fiber reinforced resin reinforcing material, cement reinforcing material, fiber reinforced rubber reinforcing material, machine tool parts, battery separator, chemical filter, etc. It exhibits excellent performance as an industrial material and can be widely applied.
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Abstract
Description
本発明は、上記高機能ポリエチレン繊維の製造方法を提供することも目的とする。該方法は、製造作業者や環境への悪影響を避ける為に、溶剤を用いない溶融紡糸法及び延伸工程を経て繊維を作製する。更に、延伸工程後の熱処理工程、更には該熱処理工程後の巻取り時の張力を精密に制御する。
本発明の高機能ポリエチレン繊維は、その極限粘度が0.8dL/g以上、好ましくは1.0dL/g以上、より好ましくは1.2dL/g以上であり、4.9dL/g以下、好ましくは4.0dL/g以下、より好ましくは2.5dL/g以下である。極限粘度を4.9dL/g以下とすることにより、溶融紡糸法での製糸や圧延成形フィルムからスプリットヤーンを得ることが容易になり、いわゆるゲル紡糸等で製糸する必要がない。そのため、製造コストの抑制、作業工程の簡略化の点で優位である。更に、製造時に溶剤を用いないため作業者や環境への影響も小さい。また製品となった繊維中の残留溶剤も存在しないため製品使用者に対する溶剤の悪影響がない。また、極限粘度を0.8dL/g以上とすることにより、ポリエチレンの分子末端基の減少により、繊維中の構造欠陥数を減少させることができる。そのため、強度や弾性率等の繊維の力学物性や耐切創性能を向上させることができる。なお、繊維中の残留溶剤濃度は、1000ppm以下が好ましく、より好ましくは500ppm以下、更に好ましくは200ppm以下である。前記残留溶剤としては、デカリン(デカヒドロナフタレン)等の炭化水素系溶剤が挙げられる。
また、前記高機能ポリエチレン繊維は、100℃における熱収縮率が、2.5%以下であることが好ましく、より好ましくは2.3%以下、更に好ましくは2.0%以下である。
動的な負荷下でも貯蔵弾性率の保持率の高い繊維は、24時間以上、50℃や80℃等の高温環境下においても、環境変化の影響を受けることが少なく、良好な物性保持率を示す。ここで、良好な物性保持率とは、100±5%の範囲内で変動することを指す。また該繊維を染色する等の熱水を用いた後加工時において、105℃における貯蔵弾性率の保持率が高い程、後加工後の力学物性低下を抑えることが可能となる。
重量平均分子量と数平均分子量との比(Mw/Mn)は、が5.0以下であることが好ましい。Mw/Mnが5.0を超えると、高分子量成分の含有により後述する延伸工程での張力が大きくなり、延伸中での糸切れが多発し好ましくない。前記比(Mw/Mn)は1.2以上が好ましく、より好ましくは1.5以上、更に好ましくは1.8以上である。上記重量平均分子量及び数平均分子量は、実施例に記載の方法により測定して求められた値を意味する。
すなわち、密度勾配管法を用いて、本発明の高機能ポリエチレン繊維の密度を測定すると、経時的にポリエチレン繊維の密度が大きくなる。これは、毛細管現象により、密度勾配管内の溶媒が、繊維の内部の細孔に存在する空気と置換したためと考えられる。
気孔率(%)=100×(直径が3nm~1μmの細孔による容積[mL]×サンプル質量[g])/{セル容積-(水銀の質量[g]/水銀の密度[g/mL])}
なお、水銀圧入法によって求められる細孔の平均直径は、走査型電子顕微鏡による観察の場合と同様、3nm以上、1μm以下であるのが好ましく、8nm以上、500nm以下がより好ましく、更に好ましくは10nm以上、200nm以下であり、更に一層好ましくは15nm以上、150nm以下である。
該有機物は、高機能ポリエチレン繊維に対して0.005質量%以上、10.0質量%以下の比率で含有させることが好ましく、より好ましくは0.05質量%以上、8.0質量%以下、更に好ましくは0.2質量%以上、5.0質量%以下である。該有機物の含有量が0.005質量%以上であると、染料の吸尽率が高くなる傾向がある。一方、その含有量が10.0質量%以下であると、繊維中の不純物としての作用が抑えられ、力学物性等の繊維特性を維持することができる。なお、高機能ポリエチレン繊維における前記の有機物の含有量は、実施例で採用するNMR法、又は、ガスクロマトグラフ法や赤外分光法より求めることができる。
上述の分散染料及び/又はポリエチレンの両方に親和性の高い有機物としては、上記例示の化合物の内1種を単独で使用してもよく、また、2種以上を組み合わせて使用してもよい。具体的なポリエーテルとしては、ポリオキシエチレン、ポリオキシブチレンが挙げられる。上記ポリエーテルの分子量は、500以上が好ましく、より好ましくは1000以上、更に好ましくは2000以上であり、100,000以下が好ましく、好ましくは50,000以下、更に好ましくは30,000以下である。分子量が100,000を超えると、粘度が大きくなり繊維全体に均一に付与することが困難になるため好ましくない。なお、本発明に係る有機物としては、上記例示の化合物の中でも、ポリエーテル化合物を少なくとも1種含むものであるのが好ましい。
この場合、延伸回数及び延伸温度が重要なだけではなく、特に固体状態での合計の延伸倍率を8倍以上(より好ましくは9倍以上、更に好ましくは10倍以上)にすることが好ましい。このとき固体状態での変形に要する時間を5分間以内(より好ましくは4分間以内、更に好ましくは3分間以内)とすることが好ましい。変形に要する時間が5分間を超えると、ポリエチレン繊維の単斜晶と斜方晶の比率、及び繊維内部の細孔構造を得ることができない。
また、巻取り張力が0.5cN/dtexを超えた場合は、繊維内部に余剰な残留応力を付与することとなる。その結果、100℃における熱収縮率が2.5%を超え、TMA(機械熱分析)における、あるいは最大収縮応力が0.4cN/dtexを超えてしまい好ましくない。また、製品の使用環境温度として想定される室温付近からポリエチレンの結晶分散温度付近の領域での収縮応力が高くなり、環境変化によって物性変化や寸法変化が発生し、更には、製品加工条件や最終製品の使用温度範囲が限定される等の制約が生じる為、好ましくない。
また巻取り時の温度は、結晶分散温度よりも5℃以上(より好ましくは10℃以上、更に好ましくは20℃以上)低い温度が好ましい。張力が上記範囲よりも大きい、または巻取り時の温度が結晶分散温度以上だと、得られる製品内部に残留応力が生じ寸法変化や力学物性変動が製品化後に生じるため好ましくない。また、製品の使用環境温度として想定される室温付近からポリエチレンの結晶分散温度付近の領域での収縮応力が高くなり、環境変化によって物性変化や寸法変化が発生し、更には、製品加工条件や最終製品の使用温度範囲が限定される等の制約が生じる為、好ましくない。
なお、有機物を付与する方法は特に限定されないが、例えば、液状の有機物、あるいは水や有機溶媒に有機物を分散、溶解させて調製した有機物溶液に未延伸糸を浸漬させる方法、前記有機物あるいは有機物溶液を未延伸糸に塗布あるいは噴霧する方法等が挙げられる。
前記染色高機能ポリエチレン繊維を使用すれば、分散染料による100℃で30分程度の簡便な染色操作でも、洗濯堅牢度(JIS L-0844のA-1号)が3級以上、あるいはドライクリーニング堅牢度(JIS L-0860のA-1法、パークロロエチレン)が3級以上の染色高機能ポリエチレン繊維が得られ、また、この染色高機能ポリエチレン繊維を使用すれば、当該染色高機能ポリエチレン繊維と同等の染色堅牢度を有する染色品も容易に得ることができる。
本発明の被覆弾性糸を使用した織編物は、当該織編物を構成する糸の内、上述被覆弾性糸を質量比で3割以上含むことが好ましい。また、被覆弾性糸としては、1.5dtex以上、220dtex以下の単糸繊度を有するものが好ましい。残りの7割以下の割合で、ポリエステル、ナイロン、アクリル等の合成繊維、綿、毛等の天然繊維、レーヨン等の再生繊維等を用いてもよい。摩擦耐久性を確保する観点からは、単糸繊度が1~4dtexのポリエステルマルチフィラメントや、同ナイロンフィラメントを用いることが推奨される。本発明のポリエチレン繊維及び/又は被覆弾性糸を使用することに加えて、これらの構成を採用することで、織編物のクープテスターのインデックス値を上記範囲とすることができる。
前記の用途は、力学物性と同時に目的に応じて多様な色目、あるいは意匠性を求められることがある。従来、無機顔料、又は有機顔料を含有する樹脂を被覆する後加工(例えば特許4041761号を参照)が施されることが多かったが、本発明の染色高機能ポリエチレン繊維を用いることによって、素材本来の風合いを損なうことなく利用することが可能となる。
温度135℃のデカリンにてウベローデ型毛細粘度管を用いて、種々の希薄溶液の比粘度を測定した。希薄溶液粘度の濃度に対するプロットから最小2乗近似で得られる直線の原点への外挿点より極限粘度を決定した。測定に際し、サンプルを約5mm長の長さにサンプルを分割又は切断し、ポリマーに対して1質量%の酸化防止剤(吉富製薬製、「ヨシノックス(登録商標) BHT」)を添加し、135℃で4時間攪拌溶解して測定溶液を調製した。
重量平均分子量Mw、数平均分子量Mn及びMw/Mnは、ゲル・パーミエーション・クロマトグラフィー(GPC)によって測定した。GPC装置としては、「GPC 150C ALC/GPC」(Waters製)を用い、カラムとしては「GPC UT802.5」(SHODEX製)を一本、「UT806M」(SHODEX製)を2本用い、検出器として示差屈折率計(RI検出器)を用いて測定した。測定溶媒は、o-ジクロロベンゼンを使用し、カラム温度を145℃とした。試料濃度は1.0mg/mlとし、200マイクロリットル注入し測定した。分子量の検量線は、ユニバーサルキャリブレーション法により分子量既知のポリスチレン試料を用いて作成されている。
万能試験機(株式会社オリエンテック製、「テンシロン万能材料試験機」)を用い、試料長200mm(チャック間長さ)、伸長速度100%/分の条件で歪-応力曲線を雰囲気温度20℃、相対湿度65%条件下で測定した。破断点での応力と伸びから強度(cN/dtex)、伸度(%)、曲線の原点付近の最大勾配を与える接線から弾性率(cN/dtex)を計算して求めた。この時、測定時にサンプルに印加する初荷重を繊維10000m当りの重さ(g)の1/10とした。なお、各値は10回の測定値の平均値を使用した。
測定繊維サンプルを70cmにカットし、両端より各々10cmの位置に、即ちサンプル長さ50cmがわかるように印をつけた。次に、繊維サンプルに荷重が印加されないようにジグにぶら下げた状態で、熱風循環型の加熱炉を用いて、温度100℃で30分間加熱した。その後、加熱炉より繊維サンプルを取り出し、室温まで十分に徐冷した後に、最初に繊維サンプルに印をつけた位置の長さを計測した。収縮率は以下の式より求めた。なお、値は2回の測定値の平均値を使用した。
収縮率(%)=100×(加熱前の繊維サンプル長さ-加熱後の繊維サンプル長さ)/(加熱前の繊維サンプル長さ)
繊維の断面試料を下記の手順で作製した。
アクリル樹脂(BUEHLER社製、「SAMPL-KWICK 473」)で包埋した試料を、断面試料作製装置(JEOL製、「クロスセクションポリッシャ(登録商標)」)を用いて加速電圧5kVで、繊維軸の直交方向を垂直に切断した。
走査電子顕微鏡(日立ハイテクノロジーズ社製、「S4800」)を用いて、加速電圧0.5kVで試料の断面を観察し、拡大倍率20,000倍で写真を撮影した。次いで、繊維の任意の断面の1μm2あたりの、直径が3nm~1μmの細孔を目視で数えた。この測定を、場所を変えて5回行い、その平均値を用いた。細孔の直径は、円形でない場合は最大径を用いた。
サンプルを室温で24時間、真空脱気を行い、前処理を行った。次に、セル容積6mLの容器にサンプル0.08gを入れ、自動ポロシメータ(MICROMERITICS社製、「オートポアIII 9420」)を用い、細孔半径が約0.0018~100μmまでの細孔分布を測定した。本測定より各細孔径に対するサンプル1gあたりの水銀の浸入体積を微分した値を得ることができる。このとき、細孔を円柱近似し、接触角を140度、水銀の表面張力を480mN/m(480dynes/cm)、水銀密度を13.5335g/mLとした。気孔率は以下の式を用いて算出した。
気孔率(%)=100×(直径が3nm~1μmの細孔による容積[mL]×サンプル質量[g])/(セル容積-(水銀の質量[g]/(水銀の密度[g/mL]))
サンプル1gを70℃の精錬液(サンプルに対し液量が50倍、「ノイゲン(登録商標)HC」(第一工業製薬社製)が2g/L)に投入し、20分間精錬した。次にサンプルを水洗し、脱水、乾燥した。
分散染料(Diacelliton fast Scarlet B(CI Disperse Red1))をイオン交換水1Lに対し、0.4000g、染色助剤(Disper TL)をイオン交換水1Lに対し1gの濃度になるように、両者をイオン交換水に溶解し染液を調製した。この染液100mLと前記精錬したサンプル1gとを三角フラスコに入れ、染液を115℃に調整したオイルバスで加熱しながら、90分間振とうさせた。このときの振とう回数は110回/分である。
次に、紫外分光光度計(日立製作所製、「ダブルビーム分光光度型 150-20型」)を用いて、波長350nm~700nmにおける該残液(a)と該原液(b)の吸光度を測定し、その最大値をそれぞれ残液の吸光度a、原液の吸光度bとした。得られた吸光度を用いて以下の式で吸尽率(DY%)を求めた。
DY(%)=(1-(残液の吸光度a)/(原液の吸光度b))×100
有機物をガスクロマトグラフ質量分析計やH-NMR測定等を用いて同定した。
次に、以下の方法で該有機物の定量測定を行った。
アセトン/ヘキサン(=5/5)の混合液を用い室温で2分間浸しサンプルを洗浄する。これを3回繰り返した後、サンプル約10mgをオルトジクロロベンゼン/C6D6(=8/2)0.6mLを135℃で溶解させた。次に、H-NMR(分光計;ブルカー・バイオスピン社製、「AVANCE500」、マグネット;オクスフオード社製)を用いて測定を行った。
X=(B/A)×1.95
測定には、熱応力歪測定装置(セイコーインスツルメント社製、「TMA/SS120C」)を用いた。長さ20mmの繊維試料に初荷重0.01764cN/dtex負荷し、昇温速度20℃/分で昇温して、最大収縮温度及び最大収縮応力、50℃、80℃における収縮応力を測定した。
105℃、80℃、50℃における貯蔵弾性率の保持率(製造例1~16)
測定には、固体粘弾性測定装置(T.A.インスツルメント社製、「DMA Q800」)を用いた。測定条件は、測定サンプル長を10mm、試料繊度を100dtexとした。測定に際し、繊維サンプルと装置チャック間での滑りや単糸のバラケが発生しないように、繊維サンプル両端を接着剤と両面テープを用いて厚紙で挟んだ。これにより測定において繊維サンプルと装置チャック間に厚紙が存在することにより、装置チャックでの滑りや単糸のバラケを抑制することが可能となる。測定開始温度を-10℃、測定終了温度を140℃、昇温速度を1.0℃/minとした。歪み量を0.04%とし、測定開始時の初荷重0.05cN/dtexとした。また、測定周波数を11Hzとした。データの解析には、「T.A.Universal Analysis」(T.A.インスツルメント社製)を用いた。このとき保持率の計算は以下の式より求めた。
105℃、80℃、50℃における貯蔵弾性率の保持率(%)=100×[(105℃、80℃、50℃の各温度における貯蔵弾性率)/(30℃における貯蔵弾性率)]
測定には、固体粘弾性測定装置(T.A.インスツルメント社製、「DMA Q800」)を用いた。測定条件は、測定サンプル長を10mm、試料繊度を約100dtexとなるように調整して使用した。測定に際し繊維サンプルと装置チャック間での滑りや単糸のバラケが発生しないように、測定サンプル両端を接着剤と両面テープを用いて厚紙で挟んだ。これにより測定において測定サンプルと装置チャック間に厚紙が存在することにより、繊維の場合、装置チャックでの滑りや単糸のバラケを抑制することが可能となる。また測定開始温度を-140℃、測定終了温度を140℃、昇温速度を1.0℃/minとした。歪み量を0.04%とし、測定開始時の初荷重0.05cN/dtexとした。また、測定周波数を11Hzとした。データの解析には、「T.A.Universal Analysis」(T.A.インスツルメント社製)を用いた。保持率は以下の式より求めた。この各温度の貯蔵率の値から、20℃の貯蔵弾性率から最も大きく変化した値を最大変化量とした。
20℃の貯蔵弾性率に対する-50℃から60℃における貯蔵弾性率の保持率(%)=100×[(-50℃から60℃の10℃ピッチの各温度における貯蔵弾性率)/(20℃における貯蔵弾性率)]
製造例1~16では、測定には、固体粘弾性測定装置(T.A.インスツルメント社製、「DMA Q800」)を用いた。測定は、-150℃から140℃の温度範囲で、昇温速度を約1.0℃/minとした。11Hzの測定周波数で得られた値より損失弾性率を計算し、温度分散を低温側より求めた。損失弾性率の値を対数で縦軸に取り、横軸を温度でプロットし、最も高温側に現れる吸収のピーク値を結晶分散温度とした。
製造例1~16では、繊維サンプルを温度60℃の加熱炉中で24時間処理した後、一昼夜冷却させて上述の強度、伸度、弾性率の測定を行った。物性保持率は以下の式より求めた。
物性保持率(%)=100×(60℃、24時間処理後の力学物性/処理前の力学物性)
製造例17~31では、繊維サンプルを温度60℃の加熱炉中で30日間処理した後、温度20℃の室内で24時間以上冷却させて上述の強度、伸度、弾性率の測定を行った。物性保持率は以下の式より算出した。
60℃、30日後の物性保持率(%)=100×(60℃、30日処理後の力学物性/処理前の力学物性)
繊維サンプル中の残留溶剤濃度の測定には、ガスクロマトグラフィー(島津製作所製)を用いた。試料の繊維10mgをガスクロマトグラフィー注入口のガラスインサートにセットした。注入口を溶剤の沸点以上に加熱し、加熱により揮発した溶剤を窒素パージでカラムに導入した。カラム温度を40℃に設定し、溶剤を5分間トラップさせた。次に、カラム温度を80℃まで昇温させた後に測定を開始した。得られたピークより、残留溶剤濃度を求めた。
耐切創性は、切断試験機(ソドマット(SODMAT)社製、「クープテスター」)を用いて評価した。
この装置の試料台にはアルミニウム箔が設けられており、この上に試料を載置した。次いで、装置に備えられた円形の刃を、走行方向とは逆方向に回転させながら試料の上を走らせた。試料が切断されると、円形刃とアルミニウム箔とが接触して通電し、耐切創性試験が終了したことを感知する。円形刃が作動している間中、装置に取り付けられているカウンターが、円形刃の回転数に連動した数値をカウントするので、その数値を記録した。
A=(サンプルテスト前の綿布のカウント値+サンプルテスト後の綿布のカウント値)/2
インデックス値=(サンプルのカウント値+A)/A
評価する各種繊維を用いて編地を得て、該編地を精錬後、染色、還元洗浄、乾燥の工程で染色編地を得て、染色堅牢度を評価した。
なお、評価用編地は、編機としてシングルニット、φ30in×18ゲージを用い、密度をC/W=19/30とした天竺編地である。
精錬条件として、「ノイゲンHC(第一工業製薬株式会社製)」を1g/L用い、浴比1:30で60℃、10分間撹拌し、次に60℃の温水で洗浄後、脱水、風乾した。
染色を以下の方法で行った。
(i)使用染料
黒色染料として「Dianix(登録商標) Black GS-E」(ダイスタージャパン株式会社製)を、青色染料として「Sumikaron(登録商標) Blue S-BG 200%」(住友化学工業株式会社製)を用いた。
(ii)染色条件
黒色に関しては、上記黒色染料を水に分散させて6%owfの濃度の染液を調製し、浴比1:10とし、青色に関しては、上記青色染料を水に分散させて2%owfの濃度の染液を調製し、浴比1:10とした。次いで、評価用編地を染液に浸漬し、これを2℃/分で昇温し100℃で30分間保持した後に、常温まで水冷後、60℃の温水で湯洗いし、排水に色がつかなくなるまで洗浄、排水を繰り返した。
(iii)還元洗浄
評価用編地に付着している余分な染料を洗い落とすために、「テックライト」(株式会社ADEKA製)0.8g/L、水酸化ナトリウム0.5g/L中で、80℃、10分間還元洗浄した。次に、60℃の温水で洗浄後、脱水、風乾した。
(i)洗濯堅牢度
JIS L-0844のA-1号(洗濯汚染)に準拠して、評価を実施した。このとき乾燥を吊干しとした。
(ii)摩擦堅牢度
JIS L-0849に準拠し、摩擦試験機II形を用い、乾燥試験と湿潤試験を実施した。
(iii)汗堅牢度
JIS-L-0846に準拠して、酸性人工汗液及びアルカリ性人工汗液にて試験を実施した。
(iv)ドライクリーニング堅牢度
JIS L-0860のA-1法に準拠し、パークロロエチレンを用いて評価を実施した。また、JIS L-0860のB-1法に準拠し、石油系による洗濯汚染評価も実施した。
繊維の比重は、密度勾配管法により測定した。
(密度勾配管の作製)
重液として水、軽液としてイソプロピルアルコールを用い、重液に軽液を少しずつ連続的に混合しながらメモリ付きのガラス管に注ぎ入れ、ガラス管の底部には重液が存在し、ガラス管の上部に行くにつれて軽液の比率が多くなるようにして密度勾配管を作製した。この密度勾配管を30℃±0.1℃の恒温槽に入れた。
次いで、比重既知のガラス玉5個以上(比重は全て異なる)を作製した密度勾配管に静かに投入し、このまま1日間静置した後、各ガラス玉と液面との距離を測定し、このとき得られた距離を縦軸、ガラス球の比重値を横軸にとったグラフを作成し(検量線)、該グラフが直線になっていることで正確な比重液が得られていることを確認した。
(比重の測定)
上述のようにして作製した密度勾配管に、繊維サンプル(試料長:6~8mm)を投入し、投入直後、5時間後、及び24時間後における繊維サンプルの液面からの位置を測定した。密度勾配管作製時に作成した検量線を使用して、サンプルの位置における比重値を求めた。
また、5時間後の比重値と比較した場合に、24時間後の比重値が増加しているものを、繊維内部の細孔が表面と連通しているものと判断した。
示差走査熱量計(T.A.インスツルメント社製、「DSC測定装置」)を用い、データの解析には、「T.A.Universal Analysis」(T.A.インスツルメント社製)を用いた。試料を5mg以下に切断し、アルミニウムパンに約2mg充填・封入した。同様の空のアルミニウムパンをリファレンスとした。測定は、不活性ガス下、50℃から200℃の温度範囲で、昇温速度を約10℃/minとした。得られた昇温DSC曲線のベースラインを補正し、ピーク面積をサンプル重量で割り返して測定融解熱量を算出し下記記載の式より結晶化度を求めた。
結晶化度(%)= 100×(測定融解熱量(J/g))/(293(J/g))
結晶成分の比率は、固体高分解能13C NMR により求めた。具体的には、「Avance400wb」(Brukerbiospin社製)により室温で測定した。磁場強度及びスピン速度は、それぞれ9.4Tと4kHzで測定した。測定パルスはDipolar decoupling (DD)/MASを用いた。試料は短冊状に切断してローターに充填した。DD/MASスペクトルは待ち時間を4300秒としてシングルパルス法(DD/MAS法)で、全成分を反映するスペクトルを測定した。低磁場側から単斜晶、斜方晶、非晶成分として波形分離を行った。単斜晶、斜方晶、非晶成分、各々のピークの面積比より比率を求めた。
極限粘度1.9dL/g、重量平均分子量120,000、重量平均分子量と数平均分子量の比が2.7である高密度ポリエチレンペレットを0.005MPaの圧力で窒素ガスを供給しているコンテナに充填した。ペレットを押出機に供給して280℃で溶融し、ノズルフィルターのメッシュ径を10μmとして、オリフィス径(ノズル径)φ0.8mm、360Hからなる紡糸口金からノズル面温度280℃で単孔吐出量0.4g/minで吐出した。吐出された糸条を10cmの保温区間を通過させ、その後40℃環境下、風速0.5m/secのクエンチ風で冷却後、紡糸速度270m/minでチーズ形状に捲き取り、未延伸糸を得た。
製造例1において、110℃、0.2秒の熱処理とした以外は、製造例1と同様にして繊維、編物、染色編地を得た。得られた繊維の物性、加速試験後の物性保持率、TMA(機械熱分析)、貯蔵弾性率の保持率、有機物の含有量、編物のインデックス値を表1に、染色堅牢度の評価結果を表3に示した。
製造例1において、110℃、0.012秒の熱処理とした以外は、製造例1と同様にして繊維、編物、染色編地を得た。得られた繊維の力学物性、加速試験後の物性保持率、TMA(機械熱分析)、貯蔵弾性率の保持率、有機物の含有量、編物のインデックス値を表1に、染色堅牢度の評価結果を表3に示した。
製造例1において、巻取り張力を0.41cN/dtexとした以外は、製造例1と同様にして繊維、編物、染色編地を得た。得られた繊維の力学物性、加速試験後の物性保持率、TMA(機械熱分析)、貯蔵弾性率の保持率、有機物の含有量、編物のインデックス値を表1に、染色堅牢度の評価結果を表3に示した。
製造例1において、紡糸速度330m/minでチーズ形状に捲き取った以外は、製造例1と同様にして未延伸糸を得た。得られた該未延伸糸を、105℃の熱風で加熱して10倍に延伸した後に、連続して120℃で0.2秒の熱処理を該延伸糸に施した後、25℃で0.22cN/dtexの張力で巻き取って繊維を得た。得られた繊維を用いて、製造例1と同様に編物、染色編地を得た。得られた繊維の物性、加速試験後の物性保持率、TMA(機械熱分析)、貯蔵弾性率の保持率、有機物の含有量、編物のインデックス値を表1に、染色堅牢度の評価結果を表3に示した。
製造例1において、窒素ガス供給圧を0.15MPa、ノズルフィルターのメッシュ径を20μmとし、未延伸糸に付与する有機物をポリプロピレングリコールに変更して未延伸糸に対し3質量%付与した以外は、製造例1と同様にして未延伸糸を得た。この有機物は分散染料、及びポリエチレンの両方に親和性の高いものである。次いで、該未延伸糸を、ローラー温度及び雰囲気温度を45℃に設定した2個の駆動ロール間で2.5倍とした以外は、製造例1と同様にして繊維を得た。得られた繊維の物性、加速試験後の物性保持率、TMA(機械熱分析)、貯蔵弾性率の保持率、有機物の含有量、編物のインデックス値を表1に、染色堅牢度の評価結果を表3に示した。
製造例1において、窒素ガス供給圧を0.5MPa、ノズルフィルターのメッシュ径を80μmとし、未延伸糸に付与する有機物をポリエチレングリコール/パラフィン(=88/12;質量比)に変更して未延伸糸に対し2質量%付与した以外は、製造例1と同様にして未延伸糸を得た。この有機物は分散染料、及びポリエチレンの両方に親和性の高いものである。該未延伸糸を、ローラー温度及び雰囲気温度を25℃に設定した2個の駆動ロール間で2.0倍で延伸し、次いで105℃の熱風で加熱して6.0倍に延伸して繊維を得た。得られた繊維の物性、加速試験後の物性保持率、TMA(機械熱分析)、貯蔵弾性率の保持率、有機物の含有量、編物のインデックス値を表1に、染色堅牢度の評価結果を表3に示した。
製造例1において、105℃、0.5秒の熱処理、0.28cN/dtexの巻取り張力とした以外は、製造例1と同様にして繊維、編物、染色編地を得た。得られた繊維の物性、加速試験後の物性保持率、TMA(機械熱分析)、貯蔵弾性率の保持率、有機物の含有量、編物のインデックス値を表1に、染色堅牢度の評価結果を表3に示した。
極限粘度1.9dL/g、重量平均分子量120,000、重量平均分子量と数平均分子量の比が2.7である高密度ポリエチレンペレットを、0.005MPaの圧力で窒素ガスを供給しているコンテナに充填した。ペレットを押出機に供給して280℃で溶融し、ノズルフィルターのメッシュ径を10μmとし、オリフィス径φ0.8mm、360Hからなる紡糸口金からノズル面温度280℃で単孔吐出量0.4g/minで吐出した。吐出された糸条を10cmの保温区間を通過させ、その後40℃、風速0.5m/secのクエンチ風で冷却後、オクタポリエーテル/エチレングリコール(=80/20;質量比)の混合液を該未延伸糸に対し、2質量%付与して紡糸速度270m/minでチーズ形状に捲き取り、未延伸糸を得た。
得られた該未延伸糸を1日静置後、ローラー温度及び雰囲気温度を65℃に設定した2個の駆動ロール間で2.5倍、次いで105℃の熱風で加熱して4.8倍に延伸した後に、25℃で0.22cN/dtexの張力で巻き取って繊維を得た。得られた繊維の物性、加速試験後の物性保持率、TMA(機械熱分析)、貯蔵弾性率の保持率、有機物の含有量、編物のインデックス値を表2に示した。熱処理を施さず得られた繊維は物性保持率が低く、熱収縮率やTMAの収縮応力が高い数値を示し、寸法安定性が悪いことがわかった。
製造例9において、60℃、0.2秒の熱処理を施した以外は、製造例9と同様にして繊維を得た。得られた繊維の物性、加速試験後の物性保持率、TMA(機械熱分析)、貯蔵弾性率の保持率、有機物の含有量、編物のインデックス値を表2に示した。得られた繊維は物性保持率が低く、また、熱収縮率やTMAの収縮応力が高い数値を示し寸法安定性も悪かった。熱処理が不十分で、繊維内部の残留応力が除去し切れていないことがわかった。
製造例9において、120℃、0.005秒の熱処理を施した以外は、製造例9と同様にして繊維を得た。得られた繊維の物性、加速試験後の物性保持率、TMA(機械熱分析)、貯蔵弾性率の保持率、有機物の含有量、編物のインデックス値を表2に示した。得られた繊維は物性保持率が低く、また、熱収縮率やTMAの収縮応力が高い数値を示し、寸法安定性も悪かった。熱処理が不十分で、繊維内部の残留応力が除去し切れていないことがわかった。
製造例9において、120℃、0.2秒の熱処理を施し、巻取り張力0.55cN/dtexとした以外は、製造例9と同様にして繊維を得た。得られた繊維の物性、加速試験後の物性保持率、TMA(機械熱分析)、貯蔵弾性率の保持率、有機物の含有量、編物のインデックス値を表2に示した。得られた繊維は物性保持率が低く、また、熱収縮率やTMAの収縮応力が高い数値を示し、寸法安定性も悪かった。熱処理後の高い巻取り張力により、繊維内部に応力が印加されたことがわかった。
極限粘度8.2dL/g、重量平均分子量1,020,000、重量平均分子量と数平均分子量の比が5.2の超高分子量ポリエチレンを0.005MPaの圧力で窒素ガスを供給しているコンテナに充填し、押出機に供給して300℃で溶融し、ノズルフィルターのメッシュ径を100μmとして紡糸を試みたが、ノズルから押出せず、紡糸することができなかった。
極限粘度20dL/g、重量平均分子量3,300,000、重量平均分子量と数平均分子量の比が6.3である超高分子量ポリエチレンを10質量%、及びデカヒドロナフタレン90質量%のスラリー状の混合物を、分散しながら230℃の温度に設定したスクリュー型の混練り機で溶解し、ノズルフィルターのメッシュ径を200μmにし、170℃に設定した直径0.2mm、390ホールを有する口金に計量ポンプにて単孔吐出量1.0g/minで供給した。
ノズル直下に設置したスリット上の気体供給オリフィスにて、100℃に調整した窒素ガスを1.2m/minの速度で供給し、できるだけ糸条に均等に当たるようにして、繊維表面のデカヒドロナフタレンを積極的に蒸発させた。その後、30℃に設定された空気流にて実質的に冷却し、ノズル下流に設置されたネルソン状のローラーにて50m/minの速度で引き取った。この際に糸状に含有される溶剤は、元の質量の約半分まで低下していた。
引き続き、繊維を120℃の加熱オーブン下で3倍延伸した。この時、繊維にオクタポリエーテル/エチレングリコール(=80/20;質量比)の混合液を、該延伸糸に対し、0.5質量%付与した。この繊維を149℃に設置した加熱オーブン中にて、4.0倍で延伸した。延伸後、熱処理工程を介さず、25℃で1cN/dtexで巻き取った。得られた繊維の物性、加速試験後の物性保持率、TMA(機械熱分析)、貯蔵弾性率の保持率、有機物の含有量、編物のインデックス値を表2に示す。加速試験後の物性保持率や熱収縮率、収縮応力、貯蔵弾性率の保持率は非常に良好な数値を示したが、残存溶剤が500ppmと高い数値を示した。また、繊維に細孔が確認されず、気孔率と吸尽率が非常に低かった。
更に、得られた繊維を製造例1と同様にして染色編地を作製しようとしたが、染色堅牢度を試験する程の染色ができなかったので、試験を中止した。
極限粘度0.7dL/g、重量平均分子量42,000、重量平均分子量と数平均分子量の比が5.1である高密度ポリエチレンペレットを0.005MPaの圧力で窒素ガスを供給しているコンテナに充填した。ペレットを押出機に供給して230℃で溶融し、メッシュ径10μmのノズルフィルターオリフィス径φ0.8mm、360Hからなる紡糸口金からノズル面温度230℃で単孔吐出量0.4g/minで吐出した。オクタポリエーテル/エチレングリコール(=80/20;質量比)の混合液を該未延伸糸に対し、1.0質量%付与して紡糸速度270m/minでチーズ形状に捲き取り、未延伸糸を得た。
得られた該未延伸糸を1日静置後、ローラー温度及び雰囲気温度を65℃に設定した2個の駆動ロール間で1.2倍、次いで100℃の熱風で加熱して5.0倍に延伸した後に、連続して120℃で0.2秒の熱処理を該延伸糸に施した後、25℃で0.22cN/dtexの張力で巻き取って繊維を得た。得られた繊維の物性、加速試験後の物性保持率、TMA(機械熱分析)、貯蔵弾性率の保持率、有機物の含有量、編物のインデックス値を表2に示す。得られた繊維は力学物性が低く、物性保持率も低かった。また、編物のインデックス値も低かった。また、繊維に細孔も小さく、気孔率と吸尽率が非常に低かった。
更に、得られた繊維を製造例1と同様にして染色編地を作製しようとしたが、染色堅牢度を試験する程の染色ができなかったので、試験を中止した。
製造例1において、窒素ガスの供給圧を0.9MPa、ノズルフィルターのメッシュ径を200μmとし、1段目の延伸温度を90℃とした以外は、製造例1と同様にして繊維を得た。得られた繊維の物性、加速試験後の物性保持率、TMA(機械熱分析)、貯蔵弾性率の保持率、有機物の含有量、編物のインデックス値を表1に示した。得られた繊維は有機物の含有量が非常に低かった。
更に、得られた繊維を製造例1と同様にして染色編地を作製しようとしたが、染色堅牢度を試験する程の染色ができなかったので、試験を中止した。
極限粘度1.9dL/g、重量平均分子量120,000、重量平均分子量と数平均分子量の比が2.7である高密度ポリエチレンペレットを0.005MPaの圧力で窒素ガスを供給しているコンテナに充填した。ペレットを押出機に供給して280℃で溶融し、ノズルフィルターのメッシュ径を10μmとして、オリフィス径φ0.8mm、360Hからなる紡糸口金からノズル面温度280℃で単孔吐出量0.4g/minで吐出した。吐出された糸条を10cmの保温区間を通過させ、その後40℃環境下、風速0.5m/secのクエンチ風で冷却後、紡糸速度270m/minでチーズ形状に捲き取り、未延伸糸を得た。
製造例17において、110℃、0.2秒の熱処理とした以外は、製造例17と同様にして繊維、編物、染色編地を得た。得られた繊維、編物の評価結果を表4に、染色堅牢度の結果を表6に示した。
製造例17において、110℃、0.012秒の熱処理とした以外は、製造例17と同様にして繊維、編物、染色編地を得た。得られた繊維、編物の評価結果を表4に、染色堅牢度の結果を表6に示す。
製造例17において、巻取り張力を0.41cN/dtexとした以外は、製造例17と同様にして繊維、編物、染色編地を得た。得られた繊維、編物の評価結果を表4に、染色堅牢度の結果を表6に示す。
製造例17において、紡糸速度330m/min、紡糸での変形時間を0.4minとしてチーズ形状に捲き取った以外は、製造例17と同様にして未延伸糸を得た。得られた該未延伸糸を、延伸時間を3.3minとし、105℃の熱風で加熱して10倍に延伸した後に、連続して120℃で0.2秒の熱処理を該延伸糸に施した後、25℃で0.22cN/dtexの張力で巻き取って繊維を得た。得られた繊維から、製造例17と同様に編物、染色編地を得た。繊維、編物の評価結果を表4に、染色の結果を表6に示す。
製造例17において、窒素の供給圧力を0.15MPa、ノズルフィルターのメッシュ径を20μmとし、紡糸変形時間を1.9minとした以外は、製造例17と同様にして未延伸糸を得た。得られた該未延伸糸を、ローラー温度及び雰囲気温度を45℃に設定した2個の駆動ロール間で2.5倍、次いで105℃の熱風で加熱して4.8倍に延伸した。続いて、120℃で0.2秒の熱処理を該延伸糸に施した後、35℃で0.22cN/dtexの張力で巻き取って繊維を得た。得られた繊維から、製造例17と同様に編物、染色編地を得た。繊維、編物の評価結果を表4に、染色の結果を表6に示す。
極限粘度1.9dL/g、重量平均分子量120,000、重量平均分子量と数平均分子量の比が2.7である高密度ポリエチレンペレットを、0.005MPaの圧力で窒素ガスを供給しているコンテナに充填した。ペレットを押出機に供給して280℃で溶融し、オリフィス径φ0.8mm、360Hからなる紡糸口金からノズル面温度280℃で単孔吐出量0.4g/minで吐出した。吐出された糸条を10cmの保温区間を通過させ、その後40℃、風速0.5m/secのクエンチ風で冷却後、紡糸速度270m/min、紡糸での変形時間を0.8minでチーズ形状に捲き取り、未延伸糸を得た。
製造例23において、60℃、0.2秒の熱処理を施した以外は、製造例23と同様にして繊維を得た。得られた繊維の物性、貯蔵弾性率の保持率、力学物性の保持率を表5に示す。得られた繊維は貯蔵弾性率の保持率が低く、物性保持率も低かった。延伸変形時間が長いこと、及び熱処理が不十分なために、繊維内部の残留応力が除去し切れていないことによる影響と考えられる。
製造例23において、120℃、0.005秒の熱処理を施した以外は、製造例23と同様にして繊維を得た。得られた繊維の物性、貯蔵弾性率の保持率、力学物性の保持率を表5に示す。得られた繊維は貯蔵弾性率の保持率が低く、物性保持率も低かった。延伸変形時間が長いこと、及び熱処理が不十分なために、繊維内部の残留応力が除去し切れていないことによる影響と考えられる。
製造例23において、紡糸変形時間を3.3min、120℃、0.2秒の熱処理を施し、巻取り張力0.55cN/dtexとした以外は、製造例23と同様にして繊維を得た。得られた繊維の物性、貯蔵弾性率の保持率、力学物性の保持率を表5に示す。得られた繊維は貯蔵弾性率の保持率が低く、物性保持率も低かった。熱処理後の高い巻取り張力により、繊維内部に応力が印加されたことがわかった。
極限粘度8.2dL/g、重量平均分子量1,020,000、重量平均分子量と数平均分子量の比が5.2の超高分子量ポリエチレンを用い、300℃で加熱し紡糸を試みたがノズルから吐出することができず、紡糸することができなかった。
極限粘度20dL/g、重量平均分子量3,300,000、重量平均分子量と数平均分子量の比が6.3である超高分子量ポリエチレンを10質量%、及びデカヒドロナフタレン90質量%のスラリー状の混合物を、分散しながら230℃の温度に設定したスクリュー型の混練り機で溶解し、170℃に設定した直径0.8mm、260ホールを有する口金に計量ポンプにて単孔吐出量1.0g/minで供給した。
ノズル直下に設置したスリット上の気体供給オリフィスにて、100℃に調整した窒素ガスを1.2m/minの速度で供給し、できるだけ糸条に均等に当たるようにして、繊維表面のデカヒドロナフタレンを積極的に蒸発させた。その後、30℃に設定された空気流にて実質的に冷却し、ノズル下流に設置されたネルソン状のローラーにて50m/minの速度で引き取った。この際に糸状に含有される溶剤は、元の質量の約半分まで低下していた。
引き続き、繊維を120℃の加熱オーブン下で3倍延伸した。この繊維を149℃に設置した加熱オーブン中にて、4.0倍で延伸した。延伸後、熱処理工程を介さず、25℃で1cN/dtexで巻き取った。このとき紡糸変形時間は0.5min、延伸変形時間は2.2minであった。得られた繊維の物性、貯蔵弾性率の保持率、力学物性の保持率を表5に示す。残存溶剤が1200ppmと高い数値を示した。
極限粘度0.7dL/g、重量平均分子量42,000、重量平均分子量と数平均分子量の比が5.1である高密度ポリエチレンペレットを0.005MPaの圧力で窒素ガスを供給しているコンテナに充填した。ペレットを押出機に供給して230℃で溶融し、オリフィス径φ0.8mm、360Hからなる紡糸口金からノズル面温度230℃で単孔吐出量0.4g/minで吐出した。吐出された糸条を10cmの保温区間を通過させ、その後40℃、風速0.5m/secのクエンチ風で冷却後、紡糸速度270m/minでチーズ形状に捲き取り、未延伸糸を得た。得られた該未延伸糸を、ローラー温度及び雰囲気温度を65℃に設定した2個の駆動ロール間で2.0倍、次いで100℃の熱風で加熱して4.0倍に延伸した後に、連続して120℃で0.2秒の熱処理を該延伸糸に施した後、25℃で0.22cN/dtexの張力で巻き取った以外は製造例23と同様にして繊維を得た。得られた繊維の物性、貯蔵弾性率の最大変化量を表5に示す。得られた繊維は力学物性が低く、貯蔵弾性率の保持率及び力学物性の保持率が著しく低下した。
紡糸変形時間を0.2min、延伸変形時間を5.2minにした以外は製造例17と同様にして繊維を得た。得られた繊維の物性、貯蔵弾性率の最大変化量を表5に示す。得られた繊維は貯蔵弾性率及び力学物性の保持率が大きく低下した。
紡糸変形時間を0.2min、延伸変形時間を4.8min、巻取り張力を0.58cN/dtexにした以外は製造例17と同様にして繊維を得た。得られた繊維の物性、貯蔵弾性率の保持率、力学物性の保持率を表5に示す。得られた繊維は貯蔵弾性率及び力学物性の保持率が大きく低下した。
Claims (20)
- 極限粘度[η]が0.8dL/g以上4.9dL/g以下で、その繰り返し単位が実質エチレンからなり、
TMA(機械熱分析)における最大収縮応力が0.4cN/dtex以下であり、100℃における熱収縮率が2.5%以下であることを特徴とする高機能ポリエチレン繊維。 - TMA(機械熱分析)における50℃の収縮応力が0.05cN/dtex以下、80℃における収縮応力が0.2cN/dtex以下である請求項1に記載の高機能ポリエチレン繊維。
- 極限粘度[η]が0.8dL/g以上4.9dL/g以下で、その繰り返し単位が実質エチレンからなり、
105℃における貯蔵弾性率の保持率が30℃の貯蔵弾性率に対して30%以上であることを特徴とする高機能ポリエチレン繊維。 - 80℃における貯蔵弾性率の保持率が30℃の貯蔵弾性率に対して50%以上、50℃における貯蔵弾性率の保持率が30℃の貯蔵弾性率に対して80%以上である請求項3に記載の高機能ポリエチレン繊維。
- 極限粘度[η]が0.8dL/g以上4.9dL/g以下で、その繰り返し単位が実質エチレンからなり、
-50℃から60℃の範囲内の10℃間隔での貯蔵弾性率が、20℃での貯蔵弾性率に対して60%以上130%以下であることを特徴とする高機能ポリエチレン繊維。 - 極限粘度[η]が0.8dL/g以上4.9dL/g以下で、その繰り返し単位が実質エチレンからなり、
繊維中の単斜晶の比率が0.5%以上30%以下、且つ、斜方晶の比率が40%以上90%以下であることを特徴とする高機能ポリエチレン繊維。 - 繊維中の結晶化度が、60%以上95%以下である請求項6に記載の高機能ポリエチレン繊維。
- ポリエチレンの重量平均分子量(Mw)が50,000~600,000であり、重量平均分子量と数平均分子量(Mn)の比(Mw/Mn)が5.0以下である請求項1~7のいずれか1項に記載の高機能ポリエチレン繊維。
- 引張強度が8cN/dtex以上、初期弾性率が200cN/dtex以上である請求項1~8のいずれか1項に記載の高機能ポリエチレン繊維。
- 繊維中の残留溶剤濃度が、1000ppm以下である請求項1~9のいずれか1項に記載の高機能ポリエチレン繊維。
- 繊維表面から内部にかけて細孔を有し、細孔を円柱近似し、接触角140度で水銀圧入法を用いて測定した際の細孔の平均直径が3nm~1μmで、細孔による気孔率が1.5~20%である請求項1~10のいずれか1項に記載の高機能ポリエチレン繊維。
- ポリエチレン繊維が、分散染料及びポリエチレンの両方に親和性を有する有機物を0.005~10.0質量%含有している請求項1~11のいずれか1項に記載の高機能ポリエチレン繊維。
- 分散染料及びポリエチレンの両方に親和性を有する有機物が、分子量500以上のポリエーテル化合物を少なくとも1種含有している請求項12に記載の高機能ポリエチレン繊維。
- 分散染料(Diaceliton fast Scarlet B (CI Disperse Red 1))を0.4g/L、染色助剤(Disper TL)を1g/Lの濃度に調整した染液に対し、浴比1:100にて100℃、90分間染色したときの吸尽率が17%以上である請求項1~13のいずれか1項に記載の高機能ポリエチレン繊維。
- 請求項1~14のいずれか1項に記載の高機能ポリエチレン繊維を、分散染料で染色してなることを特徴とする染色高機能ポリエチレン繊維。
- JIS L-0844のA-1号法に準じた洗濯堅牢度、及び/又は、JIS L-0860のA-1法に準じたドライクリーニング堅牢度の評価値が、3級以上である請求項15に記載の染色高機能ポリエチレン繊維。
- 請求項1~14のいずれか1項に記載の高機能ポリエチレン繊維又は請求項15若しくは16に記載の染色ポリエチレン繊維を、弾性糸にカバリングしてなることを特徴とする被覆弾性糸。
- 請求項1~14のいずれか1項に記載の高機能ポリエチレン繊維、請求項15若しくは16に記載の染色ポリエチレン繊維又は請求項17に記載の被覆弾性糸を、少なくとも一部に用いて製織編され、
クープテスターのインデックス値が2.5以上であることを特徴とする防護用織編物。 - 請求項18に記載の防護用織編物からなることを特徴とする耐切創性手袋。
- 極限粘度[η]が0.8dL/g以上4.9dL/g以下であり、その繰り返し単位が実質エチレンからなるポリエチレンを溶融紡糸し、
更にポリエチレンの結晶分散温度以上の温度で延伸した後に、
結晶分散温度よりも10℃以上高い温度で、0.01秒以上の熱処理を施した後、
0.5cN/dtex以下の張力で巻き取ることを特徴とする高機能ポリエチレン繊維の製造方法。
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CN116324056A (zh) * | 2020-12-30 | 2023-06-23 | 可隆工业株式会社 | 耐切割性聚乙烯纱线 |
TW202302943A (zh) * | 2021-05-07 | 2023-01-16 | 美商生活實驗設計公司 | 涼感紗及其製成之織物 |
KR102480920B1 (ko) * | 2021-12-08 | 2022-12-26 | 코오롱인더스트리 주식회사 | 치수안정성이 향상된 폴리에틸렌 원사 및 이를 포함하는 기능성 원단 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003528994A (ja) * | 2000-03-27 | 2003-09-30 | ハネウェル・インターナショナル・インコーポレーテッド | 高強力高モジュラスフィラメント |
WO2003085176A1 (fr) * | 2002-04-09 | 2003-10-16 | Toyo Boseki Kabushiki Kaisha | Fibre de polyethylene et procede de production de la fibre |
WO2011102186A1 (ja) * | 2010-02-19 | 2011-08-25 | 東洋紡績株式会社 | 成型加工性に優れた高機能ポリエチレン繊維 |
Family Cites Families (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3166885A (en) * | 1963-06-20 | 1965-01-26 | Deering Milliken Res Corp | Production of composite stretch yarns |
NL7304178A (ja) * | 1972-04-06 | 1973-10-09 | ||
US5171815A (en) * | 1986-10-22 | 1992-12-15 | University Of Pittsburgh | Method for producing doubly oriented polymers |
DE3850905T2 (de) * | 1987-05-06 | 1994-12-01 | Mitsui Petrochemical Industries, Ltd., Tokio/Tokyo | Molekular orientiertes geformtes Gebilde aus Ethylen-alpha-olefin-copolymer mit ultrahohem Molekulargewicht. |
JPH01293102A (ja) * | 1988-05-23 | 1989-11-27 | Tokuyama Soda Co Ltd | 微多孔性中空糸膜及びその製造方法 |
WO1993009277A1 (en) * | 1991-10-31 | 1993-05-13 | Ube-Nitto Kasei Co., Ltd. | Porous fiber and method of making thereof |
FI93865C (fi) * | 1992-05-29 | 1995-06-12 | Borealis Holding As | Sulakehrätty luja polyeteenikuitu |
JPH1160790A (ja) | 1997-08-08 | 1999-03-05 | Mitsui Chem Inc | ポリエチレン微多孔膜およびその製造方法 |
JP3666635B2 (ja) | 1999-08-30 | 2005-06-29 | 東洋紡績株式会社 | 均一性に優れた高強度ポリエチレン繊維 |
EP1350868B1 (en) | 2000-12-11 | 2007-06-27 | Toyo Boseki Kabushiki Kaisha | High strength polyethylene fiber |
JP3734077B2 (ja) | 2000-12-11 | 2006-01-11 | 東洋紡績株式会社 | 高強度ポリエチレン繊維 |
JP4389142B2 (ja) * | 2001-08-08 | 2009-12-24 | 東洋紡績株式会社 | 高強度ポリエチレン繊維の製造方法 |
JP4366626B2 (ja) * | 2001-08-09 | 2009-11-18 | 東洋紡績株式会社 | スクリーン印刷用メッシュ織編物 |
JP4066226B2 (ja) | 2001-08-09 | 2008-03-26 | 東洋紡績株式会社 | 高強度ポリオレフィン繊維およびその製造方法 |
JP3832631B2 (ja) * | 2001-08-23 | 2006-10-11 | 東洋紡績株式会社 | 高強度ポリエチレン繊維 |
US7216771B2 (en) * | 2001-09-15 | 2007-05-15 | Ronald Leslie Huish | Storage units |
CN100422399C (zh) * | 2002-04-01 | 2008-10-01 | 闫镇达 | 超高强度、超高模量聚乙烯纤维的纺制方法 |
JP5197912B2 (ja) * | 2004-11-19 | 2013-05-15 | 国立大学法人東京農工大学 | 多孔質体の製造方法 |
US20100000031A1 (en) * | 2005-12-02 | 2010-01-07 | Basf Se | Migration-stable dyes in polymeric materials via complex formation of polyisobutene derivatives with dyes |
EP2063004B1 (en) * | 2006-04-07 | 2012-04-25 | DSM IP Assets B.V. | Polyethylene fiber and method for production thereof |
US7935283B2 (en) * | 2009-01-09 | 2011-05-03 | Honeywell International Inc. | Melt spinning blends of UHMWPE and HDPE and fibers made therefrom |
-
2011
- 2011-09-14 CN CN201180004869.8A patent/CN102812170B/zh active Active
- 2011-09-14 KR KR1020137022892A patent/KR101361871B1/ko active IP Right Grant
- 2011-09-14 US US14/002,421 patent/US11155936B2/en active Active
- 2011-09-14 WO PCT/JP2011/071057 patent/WO2012117596A1/ja active Application Filing
- 2011-09-14 MY MYPI2013003222A patent/MY161188A/en unknown
- 2011-09-14 EP EP11859984.4A patent/EP2682504B1/en active Active
-
2012
- 2012-03-02 TW TW101106852A patent/TWI558869B/zh active
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003528994A (ja) * | 2000-03-27 | 2003-09-30 | ハネウェル・インターナショナル・インコーポレーテッド | 高強力高モジュラスフィラメント |
WO2003085176A1 (fr) * | 2002-04-09 | 2003-10-16 | Toyo Boseki Kabushiki Kaisha | Fibre de polyethylene et procede de production de la fibre |
WO2011102186A1 (ja) * | 2010-02-19 | 2011-08-25 | 東洋紡績株式会社 | 成型加工性に優れた高機能ポリエチレン繊維 |
Non-Patent Citations (1)
Title |
---|
See also references of EP2682504A4 * |
Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2014113727A (ja) * | 2012-12-07 | 2014-06-26 | Toyobo Co Ltd | ポリエチレンテープ、ポリエチレンスプリットヤーン及びそれらの製造方法 |
JP2014114362A (ja) * | 2012-12-07 | 2014-06-26 | Toyobo Co Ltd | ポリエチレンテープ、ポリエチレンスプリットヤーン及びそれらの製造方法 |
US10337123B2 (en) | 2014-06-18 | 2019-07-02 | E I Du Pont De Nemours And Company | Flash spun plexifilamentary strands and sheets |
US10329692B2 (en) * | 2015-07-10 | 2019-06-25 | E I Du Pont De Nemours And Company | Flash spun plexifilamentary strands and sheets |
WO2017146144A1 (ja) * | 2016-02-24 | 2017-08-31 | 東洋紡株式会社 | 着色ポリエチレン繊維およびその製造方法 |
TWI715733B (zh) * | 2016-02-24 | 2021-01-11 | 日商東洋紡股份有限公司 | 著色聚乙烯纖維、編繩、釣魚線、手套、繩索、網、針織物或編織物及著色聚乙烯纖維之製造方法 |
JP2017179684A (ja) * | 2016-03-29 | 2017-10-05 | 東洋紡株式会社 | 耐切創性に優れたポリエチレン繊維、およびそれを用いた製品 |
JP2018003230A (ja) * | 2016-06-23 | 2018-01-11 | 東洋紡株式会社 | 着色ポリエチレン繊維およびその製造方法 |
JP6992257B2 (ja) | 2016-06-23 | 2022-01-13 | 東洋紡株式会社 | 着色ポリエチレン繊維およびその製造方法 |
JP2018135627A (ja) * | 2017-02-20 | 2018-08-30 | 東洋紡株式会社 | 着色ポリエチレン繊維およびその製造方法 |
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JP7333411B2 (ja) | 2019-03-21 | 2023-08-24 | コーロン インダストリーズ インク | 耐切断性ポリエチレン原糸、その製造方法、およびこれを用いて製造された保護用製品 |
JP2022551745A (ja) * | 2019-12-27 | 2022-12-13 | コーロン インダストリーズ インク | 優れた寸法安定性を有するポリエチレン原糸およびその製造方法 |
JP7348394B2 (ja) | 2019-12-27 | 2023-09-20 | コーロン インダストリーズ インク | 優れた寸法安定性を有するポリエチレン原糸およびその製造方法 |
KR20220142746A (ko) * | 2021-04-15 | 2022-10-24 | 에쓰대시오일 주식회사 | 고온 인장 시험기의 다단 연신을 이용한 폴리올레핀계 모노필라멘트 원사의 제조방법, 이에 의해 제조된 폴리올레핀계 모노필라멘트 원사 및 상기 폴리올레핀계 모노필라멘트 원사의 물성 예측방법 |
KR102486793B1 (ko) | 2021-04-15 | 2023-01-10 | 에쓰대시오일 주식회사 | 고온 인장 시험기의 다단 연신을 이용한 폴리올레핀계 모노필라멘트 원사의 제조방법, 이에 의해 제조된 폴리올레핀계 모노필라멘트 원사 및 상기 폴리올레핀계 모노필라멘트 원사의 물성 예측방법 |
Also Published As
Publication number | Publication date |
---|---|
US11155936B2 (en) | 2021-10-26 |
CN102812170B (zh) | 2015-04-22 |
TWI558869B (zh) | 2016-11-21 |
EP2682504B1 (en) | 2017-05-17 |
MY161188A (en) | 2017-04-14 |
EP2682504A1 (en) | 2014-01-08 |
US20140000007A1 (en) | 2014-01-02 |
TW201245520A (en) | 2012-11-16 |
EP2682504A4 (en) | 2014-09-10 |
KR101361871B1 (ko) | 2014-02-12 |
CN102812170A (zh) | 2012-12-05 |
KR20130117872A (ko) | 2013-10-28 |
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