WO2005033383A1 - Vinyl chloride based fiber and method for production thereof - Google Patents

Vinyl chloride based fiber and method for production thereof Download PDF

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Publication number
WO2005033383A1
WO2005033383A1 PCT/JP2004/013215 JP2004013215W WO2005033383A1 WO 2005033383 A1 WO2005033383 A1 WO 2005033383A1 JP 2004013215 W JP2004013215 W JP 2004013215W WO 2005033383 A1 WO2005033383 A1 WO 2005033383A1
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WO
WIPO (PCT)
Prior art keywords
mass
vinyl chloride
parts
fiber
epoxidized
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PCT/JP2004/013215
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French (fr)
Japanese (ja)
Inventor
Atsushi Horihata
Akira Moroi
Original Assignee
Denki Kagaku Kogyo Kabushiki Kaisha
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Application filed by Denki Kagaku Kogyo Kabushiki Kaisha filed Critical Denki Kagaku Kogyo Kabushiki Kaisha
Priority to US10/574,178 priority Critical patent/US20070009735A1/en
Priority to JP2005514381A priority patent/JPWO2005033383A1/en
Publication of WO2005033383A1 publication Critical patent/WO2005033383A1/en

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Classifications

    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F1/00General methods for the manufacture of artificial filaments or the like
    • D01F1/02Addition of substances to the spinning solution or to the melt
    • D01F1/10Other agents for modifying properties
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/02Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D01F6/08Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polymers of halogenated hydrocarbons
    • D01F6/10Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polymers of halogenated hydrocarbons from polyvinyl chloride or polyvinylidene chloride
    • DTEXTILES; PAPER
    • D10INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10BINDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B2321/00Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D10B2321/04Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds polymers of halogenated hydrocarbons
    • D10B2321/041Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds polymers of halogenated hydrocarbons polyvinyl chloride or polyvinylidene chloride
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/29Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2913Rod, strand, filament or fiber

Definitions

  • Vinyl chloride fiber and method for producing the same
  • the present invention relates to a chloride-based fiber having a brow, a hue, and a texture resembling human hair used in the manufacture of hair decoration products such as wigs, hair pieces, blades, extension hair and the like. .
  • a vinyl chloride-based fiber obtained by spinning a polyvinyl chloride-based resin in the past is excellent in transparency and flexibility, and thus it is often used as a fiber for artificial hair constituting a hair decoration product. It is used.
  • Wet spinning methods and dry spinning methods are known as the above-mentioned "method using a solvent”
  • melt spinning methods are known as the above-mentioned "method using no solvent”.
  • a salt-like resin has a high melt viscosity and an extremely low spinnability, so a salt-like resin is melt-spun to obtain a certain quality of vinyl chloride fiber. There was a problem that it was difficult to do.
  • the salt-and-boil type resin is desalted into the salt-and-vinyl polymer that constitutes a salt-type resin when exposed to high temperature environments and exposed to sunlight and ultraviolet light. As a hydrogen peroxide reaction occurs, chloride-based fibers composed of chloride-based resins are 1) poor in initial colorability, and 2) easily become strong yellowish fibers. 3) There was a problem that the product value might be reduced.
  • a vinyl chloride-based resin consisting of 100 to 60% by weight of vinyl chloride-based resin and 0 to 40% by weight of chlorinated chloride-based resin.
  • a chloride-based boule-based fiber has been proposed which also has the strength of a salt-like bole-based resin composition (see Patent Document 1).
  • tin is used as the heat stabilizer (b).
  • Patent Document 1 Japanese Patent Application Laid-Open No. 11-100714
  • melt spinning using a vinyl chloride resin composition containing the above-mentioned “hydrode-talcite-based heat stabilizer” a metal mesh in a melt spinning machine may be used. Since the carbides are clogged, the frequency of thread breakage further increases and spinning becomes difficult, and there is a problem that continuous melt spinnability, that is, long runnability of melt spinning becomes worse. There is also a problem that the vinyl chloride-based fiber containing the hyd- ide-talcite-based heat stabilizer as a component discolors when it is curled by applying heat.
  • the present invention aims to solve these problems.
  • a long-passing property of melt spinning is secured by using an iron- and / or id-portal heat-stable stabilizer, and good and stable productivity can be obtained. It is an object of the present invention to provide a salt-like fiber and a method for producing the same, which causes little discoloration even when
  • the inventors of the present invention investigated the cause of the above problems: 1) The vinyl resin composition containing the above-mentioned "hydrite-talcite-based heat stabilizer” The fact that carbides of chloride-based resins are clogged in a wire mesh in a melt-spinning machine during melt spinning using a melt spinning machine, and 2) vinyl chloride containing the above-mentioned "hydrite-talcite-based heat stabilizer” as a component When heat is applied to the base fiber to cause curling, the problem of discoloration of the salt-bullet base fiber is It has been found that it is caused by the poor dispersion of the id mouth talcite heat stabilizer.
  • the inventors of the present invention have, based on strong findings, (a) 100 parts by mass of a salt-based grease, and (b) a heat stabilizer based on an id-portal talc 0.2-5.
  • a heat stabilizer based on an id-portal talc 0.2-5.
  • epoxy compound 0.2.10-10.0 parts by mass was added to the vinyl chloride-based resin composition containing 0 parts by mass, a hydride-talcite-based heat stabilizer was used.
  • the invention described in claim 2 relates to the invention described in claim 1, wherein the epoxy compound is an epoxy-based soybean oil, an epoxidized linseed oil, an epoxy-based soybean oil, an epoxy-based fish oil, an epoxy-based beef oil.
  • Epoxidized animal and animal oils Epoxidized animal and animal oils, epoxy-containing methacrylic acid compounds, epoxidized methyl stearate, epoxy butadiene polybutadiene, tris (epoxypropyl) isocyanurate, epoxy oil Fatty acid ester, epoxidized linseed oil fatty acid ester, vinyl chlorohexene epoxide, dicyclohexene carboxylate, bisphenol A diglycidyl ether, glycerin polyglycidyl ether, and cyclohexane dimethanol polyglycidyl ether power It is characterized in that at least one of Epokishii ⁇ thereof.
  • the invention described in claim 3 relates to the invention described in claim 1 or 2, wherein the chlorinated boule-based resin composition further comprises (d) a nitrogen-containing polyol 0. 01-2. It is characterized in that it contains 0 parts by mass.
  • the invention described in claim 4 relates to the invention described in claim 3, wherein the nitrogen-containing polyol is tris (2-hydroxyethyl) isocyanurate, tris (3-hydroxy propyl) isocyanurate, Alternatively, it is characterized by being tris (4-hydroxybutyl) isocyanurate.
  • the invention described in claim 5 is as follows: (a) 100 parts by mass of a salt-and-bure based resin, (b) a hydifice-based thermal stabilizer 0.2-5. 0 parts by mass, and (C) Epoxy compound: A salt-based resin composition containing 0.2 to 10.0 parts by mass is melt-spun at a temperature of 170 to 190 ° C.
  • the invention described in claim 6 is the method according to the invention described in claim 5, under the atmosphere of air in which the melt spun chloride-based boule fiber is maintained at a temperature of 90-120 ° C. — After being drawn to 4 times, this drawn chloride-based fiber is kept at a temperature of 110-140 ° C. until it shrinks to a length of 60-100% of the fiber length of the drawn fiber under an air atmosphere It is characterized by heat relaxation.
  • the chlorinated boule-based resin composition further comprises (d) a nitrogen-containing polyol 0. 01-2. It is characterized in that it contains 0 parts by mass.
  • the vinyl chloride resin composition further comprises (d) a nitrogen-containing polyol in an amount of 0.1-2 parts by mass. Because of the synergistic effect with the epoxy compound, the effect of suppressing color change when heat is applied in the curling step can be improved.
  • the vinyl chloride resin composition further comprises (d) 0.1 to 20 parts by mass of a nitrogen-containing polyol. Because of the synergistic effect with the epoxy compound, the effect of suppressing discoloration when heat is applied in the curling step can be improved.
  • the vinyl chloride-based fiber of the present invention comprises (a) 100 parts by mass of a vinyl chloride-based resin, (b) a thermal stabilizer based on hydrotalcite, and 0.5 to 2.0 parts by mass, (C) Epoxy compound It is composed of a vinyl chloride resin composition containing 0.2 to 10.0 parts by mass.
  • the above-mentioned "vinyl chloride-based resin” is obtained by bulk polymerization, solution polymerization, suspension polymerization, emulsion polymerization and the like of (i) vinyl chloride, and the polymerization method thereof
  • polyvinyl chloride, chlorinated polyvinyl chloride, polyvinyl chloride, polyvinyl chloride, chlorinated polyethylene, chloride-vinyl acetate copolymer, chloride-vinyl chloride, and the like are examples of polyvinyl chloride, chlorinated polyvinyl chloride, polyvinyl chloride, chlorinated polyethylene, chloride-vinyl acetate copolymer, chloride-vinyl chloride, and the like.
  • Ruethylene copolymer vinyl chloride-propylene copolymer, butyl chloride-styrene copolymer, chloride-bullet isobutylene copolymer, chloride-polyether-biarylidene copolymer, chloride-bistyrene copolymer, anhydrous Maleic acid terpolymers, vinyl styrene-acrylonitrile terpolymers, vinyl chloride-butadiene copolymers, vinyl isoprene copolymers, vinyl chloride-chlorinated propylene copolymers, Shiojibi-bi -Salt byluriden acetate-Bullet acetate terpolymer, Chloride burl-Maleic ester copolymer, Chloride-Bryl methacrylate ester copolymer, Chloride-Bryl-Acrylonitrile copolymer, Chloride-Bivinyl various Chlorine-containing resins such as boule ether
  • block copolymers which contain chloride chloride and graft copolymers which contain sodium chloride.
  • salt-based vinyl fat composition for fibers may be blended with known additives used in conventional salt-vinyl based compositions.
  • additives include, for example, plasticizers, lubricants, compatibilizers, processing aids, toughening agents, UV absorbers, antioxidants, antistatic agents, fillers, flame retardants, pigments, initial color improvers, conductive agents. Gendering agents, surface treatment agents, light stabilizers, and perfumes.
  • the chlorine burle-based fiber of the present invention preferably has a thickness of 20 to 100 denier, more preferably 50 to 80 denier.
  • a thickness of 20 to 100 denier more preferably 50 to 80 denier.
  • the cross-sectional shape of the vinyl chloride-based fiber of the present invention may be any shape, for example, circular, oval, glasses, star, H-shaped, double-sided, Y-shaped, triangle, square, cross, heart It may be a shape, a horseshoe shape, or a combination of these. Also, these hollow bodies may be used.
  • the "noid-in-mouth-talcite-based heat stabilizer” in the present invention does not have the problem of adversely affecting the microorganisms in the environment or generating an odor like the organotin-based heat stabilizer, There is no toxicity.
  • such "noid-opening-talcite-based heat stabilizers” are compounds with a light-opening-talcite compound, and more specifically, magnesium and z or an alkali metal and aluminum, zinc, magnesium, or magnesium. It is a composite salt compound that also has aluminum power.
  • some of their complex salts are those obtained by dehydrating the compound crystal water.
  • the high mouth talcite compound may be a natural product or a synthetic product, but as a synthetic method of the synthetic product, a conventionally known method may be used.
  • the yarn breakage frequency increases when the blending amount of the gauze and lidoguchi heat-site-based heat stabilizer is less than 0.2 parts by mass, and the gauze and i-domouth talcite-based heat resistance Stabilizer formulation If the amount is more than 5.0 parts by mass, the initial colorability is deteriorated. Therefore, in the present invention, the blending amount of the above-mentioned hyd- ide-talcite-based heat stabilizer is preferably 0.2-5. 0 parts by mass, and more preferably 0.5-5. 0 parts by mass. It is.
  • the "epoxy compound" in the present invention is preferably epoxy soybean oil, epoxy soybean linseed oil, epoxy soybean oil, epoxidized fish oil, epoxy oil calf oil, epoxy oil castor oil, epoxy oil safflower Epoxides and oils such as oil and vegetable oils, epoxy-containing methacrylic acid compounds, epoxidized methyl stearate, epoxidized polybutadiene, tris (epoxypropyl) isocyanurate, epoxidized tall oil fatty acid ester, epoxidized linseed oil fatty acid ester, And at least one epoxy compound selected from biphenyl hexahexene, dicyclohexene carboxylate, bisphenol A diglycidyl ether, glycerin polyglycidyl ether, and cyclohexane dimethanol polyglycidyl ether. That is, as long as it 's Chikarama be epoxy compounds other than these Epokishii
  • the compounding amount of the “epoxy compound” when the compounding amount of the “epoxy compound” is less than 0.2 parts by mass, the effect of improving the long-run property of melt spinning or the color change suppressing effect of the vinyl chloride fiber produced can be improved.
  • the fruit becomes smaller, and when the blending amount of the epoxy compound is more than 10.0 parts by mass, the frequency of thread breakage increases. Therefore, in the present invention, the compounding amount of the epoxy compound is preferably 0.2 to 10.0 parts by mass, more preferably 0.5 to 30.0 parts by mass.
  • the salt-and-brull-based resin composition may further contain (d) 0.1 to 20 parts by mass of a nitrogen-containing polyol.
  • a nitrogen-containing polyol in an amount of 0.1 to 2 parts by mass, curling is imparted due to the synergistic effect with the epoxy compound. The effect of suppressing color change when heat is applied in the process can be greatly improved.
  • the nitrogen-containing polyol is preferably tris (2-hydroxyethyl) isocyanurate, tris (3-hydroxypropyl) isocyanurate, or tris (4-hydroxybutynore) isocyanurate. Even if it is an epoxy compound other than these nitrogen-containing polyols, unless it is against the purpose.
  • the blending amount of the nitrogen-containing polyol is less than 0.01 parts by mass, the effect of reducing the color change when heat is applied in the curling step becomes poor, and the nitrogen If the blending amount of the contained polyol is more than 2.0 parts by mass, the yarn breakage frequency is increased. Therefore, in the present invention, the blending amount of the nitrogen-containing polyol is preferably 0.01 to 2.0 parts by mass, and more preferably 0.02 to 1.0 parts by mass.
  • the vinyl chloride-based fiber of the present invention is preferably (a) 100 parts by mass of vinyl chloride-based resin, (b) thermal stabilizer based on hyde-portal talc 0.2-5.
  • a vinyl chloride resin composition containing 0 parts by mass and (c) 0.20 parts by mass of epoxy compound at a temperature of 170 to 190 ° C.
  • epoxy compound 0 Melt-spinning of a chloride-based resin composition containing 2 to 10 parts by mass at a temperature of 170 to 190 ° C.
  • a powder compound is prepared by mixing the above-mentioned "vinyl chloride resin composition" using a mixer such as a Henschel mixer, a ribbon platen, etc., Alternatively, a pellet compound obtained by melt-mixing the same is melted at a temperature of 170-190 ° C. using a melt extruder such as a single-screw extruder, a counter-rotating twin-screw extruder, or a co-Carni shaft extruder. It is manufactured by spinning.
  • a melt extruder such as a single-screw extruder, a counter-rotating twin-screw extruder, or a co-Carni shaft extruder. It is manufactured by spinning.
  • the melt-spun vinyl chloride-based fiber is stretched to 2 to 4 times in an air atmosphere maintained at a temperature of 90 to 120 ° C.
  • the drawn vinyl chloride fiber is thermally relaxed in an air atmosphere maintained at a temperature of 110-140 ° C. to a length of 60-100% before treatment.
  • the chloride-based resin composition preferably further includes (d) a nitrogen-containing polyol of 0.1 to 20 parts by mass. Can be contained.
  • the salt-to-water vinyl-based resin composition further has (d) nitrogen-containing polyol 0.1 to 20 parts by mass, the synergy with the epoxy compound is obtained. By the effect, it is possible to improve the suppression effect of color change when heat is applied in the curling process. Ru.
  • Example 2 The same procedure as in Example 1 was repeated except that 0.5 parts by mass of (d) nitrogen-containing polyol (NF-SE, manufactured by Nissan Chemical Co., Ltd.) was added to the salt-bure based resin composition. A salt-based fiber was obtained.
  • NF-SE nitrogen-containing polyol
  • Example 1 was repeated except that 5 parts by mass of (d) nitrogen-containing polyol (NF-SE, manufactured by Nissan Chemical Co., Ltd.) was added to the salt-to-bule type resin composition in the same manner as in Example 1 above. System fiber was obtained.
  • NF-SE nitrogen-containing polyol
  • NF-12 Zn 0.8 part by mass
  • the melt-spinning was carried out with a nozzle cross-sectional area of 0.06 mm 2 , a hole number of 120, and a mold temperature of 175 ° C. by an extrusion amount of lOKgZ time, and a vinyl chloride fiber of an average fineness of 135 denier. I asked.
  • this drawn fiber is 75% of the fiber length of the drawn fiber in an air atmosphere at 110 ° C.
  • the mixture was heat-relaxed until it shrunk to give a vinyl chloride-based fiber having an average fineness of 60 denier.
  • Example 1-13 and Comparative Example 1-14 of vinyl chloride-based fibers obtained in (4) Longura Colorability, (mouth) discoloration, (ha) yarn breakage frequency, and (ii) initial colorability were evaluated.
  • the evaluation results are shown in Table 1 below.
  • the “long run property” in the above item (b) represents continuous melt spinning time until a state in which production can not be performed unless the wire mesh is replaced due to frequent occurrence of thread breakage during melt spinning. And the evaluation criteria are
  • the “discoloring property” in the above (mouth) is a characteristic value for determining the degree of discoloration at the time of the curling step! / ,.
  • This “discoloring property” is a color difference meter (Kurashiki Spinning Co., Ltd.) after heat treatment in a gear oven at 105 ° C. for 1 hour in a state of tensioning vinyl chloride based fibers before and after heat treatment.
  • the b value before heat treatment measured by color measurement with a high-accuracy spectrophotometer COLOR-7X (Here, the b value is the value measured under the light reception condition of 'illumination based on the condition b of JIS Z 8722. B) and b after heat treatment is b, the difference between b and b, A b,
  • the "thread breakage frequency" in the above (iii) is the number of occurrences of single yarn breakage when melt spinning is carried out, but converted to the yarn breakage frequency per hour (number of times Z hours),
  • the “initial colorability” in the above (2) is the force with which the color of the yarn immediately after melt-spinning is visually evaluated.
  • Example 1 The chloride-type fiber obtained in Example 1 gave a vinyl chloride-type target fiber, which is good for all properties.
  • the salted fibers obtained in Example 2 are those obtained by blending the polyol in the composition of Example 1 and having a slight difficulty in the color changeability. With respect to all the characteristic values
  • the vinyl chloride-based fiber obtained in Example 3 has some difficulty in the thread breakage frequency compared to the vinyl chloride-based fiber obtained in Example 1, but all the characteristic values have problems as a product. It was in the range.
  • the salted boule fiber obtained in Comparative Example 1 has a high content of yarn breakage frequency and is difficult to be spun because the compounding amount of the hydride-talcite-based heat stabilizer is small, so that the long run property is obtained. Was bad.
  • the salted boule based fibers obtained in Comparative Example 2 had poor initial colorability because the blending amount of the hydrotalcite-based heat stabilizer was too large.
  • the chloride-based fiber obtained in Comparative Example 3 had a long-running property and a discoloring property because the blending amount of the epoxy compound was small.
  • the chloride-based fiber obtained in Comparative Example 4 has a high yarn breakage frequency due to too much compounding amount of the epoxy compound, which makes spinning difficult, and the long-run property is bad. It was
  • the chloride-based boule fiber of the present invention has a salt, for example, having wrinkles, hues, and a texture similar to human hair used in the production of hair decoration products such as wigs, hairpieces, blades, and fixture hairs. It can be an ibule based fiber.

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  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Textile Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Artificial Filaments (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

A vinyl chloride based fiber which comprises a vinyl chloride based resin composition comprising 100 parts by mass of (a) a vinyl chloride based fiber, 0.2 to 5.0 parts by mass of (b) a hydrotalcite based heat stabilizer and 0.2 to 10.0 parts by mass of (c) an epoxy compound. Incorporation of 0.2 to 10.0 parts by mass of (c) an epoxy compound into the above vinyl chloride based resin composition improves the dispersibility of the hydrotalcite based heat stabilizer, which results in the securement of a long-running continuous operation of a melt spinning process and in the achievement of good and stable productivity in the case of the use of a hydrotalcite based heat stabilizer, and also allows the production of a vinyl chloride based fiber exhibiting reduced discoloration when heated in a step of curling.

Description

明 細 書  Specification
塩化ビニル系繊維及びその製造方法  Vinyl chloride fiber and method for producing the same
技術分野  Technical field
[0001] 本発明は、ウイッグ、ヘアピース、ブレード、エクステンションヘアー等の頭髪装飾製 品の製造において用いられる人毛に似た艷、色相、及び、風合いを有する塩化ビ- ル系繊維に関するものである。  The present invention relates to a chloride-based fiber having a brow, a hue, and a texture resembling human hair used in the manufacture of hair decoration products such as wigs, hair pieces, blades, extension hair and the like. .
背景技術  Background art
[0002] 従来、塩ィ匕ビュル系榭脂を紡糸して得た塩ィ匕ビニル系繊維は、透明性及び柔軟性 に優れているので、頭髪装飾製品を構成する人工毛髪用繊維として、多く使用され ている。この人工毛髪用繊維を工業的に製造するには、溶剤を用いる方法と溶媒を 使用しない方法とがある。前記「溶剤を用いる方法」としては、湿式紡糸法及び乾式 紡糸法が知られており、また、前記「溶媒を使用しない方法」としては、溶融紡糸法が 知られている。  [0002] A vinyl chloride-based fiber obtained by spinning a polyvinyl chloride-based resin in the past is excellent in transparency and flexibility, and thus it is often used as a fiber for artificial hair constituting a hair decoration product. It is used. There are a method using a solvent and a method not using a solvent to industrially produce this artificial hair fiber. Wet spinning methods and dry spinning methods are known as the above-mentioned "method using a solvent", and melt spinning methods are known as the above-mentioned "method using no solvent".
[0003] 塩ィ匕ビュル系榭脂は、溶融粘度が高ぐ且つ、曳糸性が極めて低いので、塩ィ匕ビ -ル系榭脂を溶融紡糸して一定品質の塩ィ匕ビニル繊維とすることは、難し 、と 、う問 題があった。そして、塩ィ匕ビュル系榭脂は、高温の環境下におかれたり、また、 日光 や紫外線に曝されると、塩ィ匕ビュル系榭脂を構成する塩ィ匕ビニル重合体に脱塩ィ匕水 素反応が生じるので、塩ィ匕ビ二ル系榭脂で構成される塩ィ匕ビュル系繊維は、 1)初期 着色性が劣ること、 2)黄色味の強い繊維になり易いこと、 3)商品価値を低下させる 場合があること、といった問題があった。  [0003] A salt-like resin has a high melt viscosity and an extremely low spinnability, so a salt-like resin is melt-spun to obtain a certain quality of vinyl chloride fiber. There was a problem that it was difficult to do. The salt-and-boil type resin is desalted into the salt-and-vinyl polymer that constitutes a salt-type resin when exposed to high temperature environments and exposed to sunlight and ultraviolet light. As a hydrogen peroxide reaction occurs, chloride-based fibers composed of chloride-based resins are 1) poor in initial colorability, and 2) easily become strong yellowish fibers. 3) There was a problem that the product value might be reduced.
[0004] そこで、力かる問題を解決するために、塩ィ匕ビ二ル系榭脂 100— 60重量%と塩素 化塩ィ匕ビュル系榭脂 0— 40重量%からなる塩ィ匕ビニル系混合物 100重量部に対し て、 (a)エチレン 酢酸ビュル系榭脂を 1一 35重量部と、(b)熱安定剤 0.2— 5.0重量 部と、(c)滑剤 0.2— 5.0重量部とを配合してなる塩ィ匕ビュル系榭脂組成物力もなる 塩化ビュル系繊維が提案された (特許文献 1を参照。 ) 0そして、前記特許文献 1には 、前記熱安定剤 (b)として、スズ系熱安定剤、 Ca-Zn系熱安定剤、ハイド口タルサイト 系熱安定剤、及び、ゼォライト系熱安定剤力 なる群の内から選択される少なくとも 1 種を用いることが開示されて 、る。 [0004] Therefore, in order to solve the pressing problem, a vinyl chloride-based resin consisting of 100 to 60% by weight of vinyl chloride-based resin and 0 to 40% by weight of chlorinated chloride-based resin. A mixture of (a) 35 parts by weight of (a) ethylene-butyl acetate based resin, (b) 0.2 to 5.0 parts by weight of a heat stabilizer, and (c) 0.2 to 5.0 parts by weight of a lubricant per 100 parts by weight of the mixture. In addition, a chloride-based boule-based fiber has been proposed which also has the strength of a salt-like bole-based resin composition (see Patent Document 1). 0 And, in Patent Document 1, tin is used as the heat stabilizer (b). System heat stabilizer, Ca-Zn system heat stabilizer, hydrotalcite-based heat stabilizer, and zeolitic system heat stabilizer at least one selected from the group consisting of The use of seeds is disclosed.
特許文献 1:特開平 11-100714号公報  Patent Document 1: Japanese Patent Application Laid-Open No. 11-100714
発明の開示  Disclosure of the invention
発明が解決しょうとする課題  Problem that invention tries to solve
[0005] しカゝしながら、前記「熱安定剤」として例示されて ヽるスズ系熱安定剤(有機スズ系 安定剤)を含有する塩ィ匕ビュル系榭脂組成物を用いて溶融紡糸する場合には、有 機スズ系安定剤が環境に排出されると、生態系に悪影響を及ぼしたり、独特の臭気 を放っという問題があった。そして、前記「スズ系熱安定剤」以外の熱安定剤を含有 する塩ィ匕ビ二ル系榭脂組成物を用いて溶融紡糸する場合には、製造時の糸切れ、 初期着色性等の面力 満足できる性能の塩ィ匕ビニル系繊維が得られな 、と 、う問題 かあつた。 Melt-spinning using a salt-based resin composition containing a tin-based heat stabilizer (organotin-based stabilizer) exemplified as the above-mentioned “heat stabilizer”. If organic tin stabilizers are discharged into the environment, there is a problem that they adversely affect the ecosystem and emit unique odors. And when melt spinning using a polyvinyl chloride resin composition containing a heat stabilizer other than the above-mentioned “tin-based heat stabilizer”, breakage of yarn at the time of production, initial colorability, etc. Facet It is difficult to obtain a vinyl chloride-based vinyl fiber with satisfactory performance.
[0006] また、前記「ハイド口タルサイト系熱安定剤」を含有する塩化ビニル系榭脂組成物を 用いて溶融紡糸する場合には、溶融紡糸機械内における金網に塩ィヒビ二ル系榭脂 の炭化物が詰まるので、糸切れ頻度がいっそう増えて紡糸が困難となり、そのために 、連続溶融紡糸性、即ち、溶融紡糸のロングラン性が悪くなるという問題があった。ま た、このハイド口タルサイト系熱安定剤を構成成分に含む塩ィ匕ビニル系繊維は、熱を 加えてカールさせる際に、変色するという問題もあった。  In the case of melt spinning using a vinyl chloride resin composition containing the above-mentioned “hydrode-talcite-based heat stabilizer”, a metal mesh in a melt spinning machine may be used. Since the carbides are clogged, the frequency of thread breakage further increases and spinning becomes difficult, and there is a problem that continuous melt spinnability, that is, long runnability of melt spinning becomes worse. There is also a problem that the vinyl chloride-based fiber containing the hyd- ide-talcite-based heat stabilizer as a component discolors when it is curled by applying heat.
[0007] 本発明は、これらの問題を解決することを目的としている。  [0007] The present invention aims to solve these problems.
[0008] 即ち、本発明は、ノ、イド口タルサイト系熱安定剤を使用し、溶融紡糸のロングラン性 が確保されて、良好で安定した生産性が得られ、しかも、カール付与工程で熱を加え ても、変色が少な 、塩ィ匕ビュル系繊維及びその製造方法を提供することを目的とし ている。  That is, according to the present invention, a long-passing property of melt spinning is secured by using an iron- and / or id-portal heat-stable stabilizer, and good and stable productivity can be obtained. It is an object of the present invention to provide a salt-like fiber and a method for producing the same, which causes little discoloration even when
課題を解決するための手段  Means to solve the problem
[0009] 本発明者らは、前記問題が生じる原因 ¾|¾意探究したところ、 1)前記「ハイド口タル サイト系熱安定剤」を含有する塩ィ匕ビ二ル系榭脂組成物を用いて溶融紡糸する際に 、溶融紡糸機械内における金網に塩ィヒビ二ル系榭脂の炭化物が詰まること、及び、 2 )前記「ハイド口タルサイト系熱安定剤」を構成成分に含む塩化ビニル系繊維に熱を 加えてカールさせる際に、該塩ィ匕ビュル系繊維が変色すること、といった問題が、ハ イド口タルサイト系熱安定剤の分散不良によって生じることを見出した。そして、本発 明者らは、力かる知見に基づいて、(a)塩ィ匕ビュル系榭脂 100質量部、及び、(b)ノ、 イド口タルサイト系熱安定剤 0. 2-5. 0質量部を含有する塩化ビニル系榭脂組成物 に、(c)エポキシィ匕合物 0. 2— 10. 0質量部を含有させたところ、ハイド口タルサイト 系熱安定剤を使用しても、溶融紡糸のロングラン性が確保されて、良好で安定した生 産性が得られ、しかも、カール付与工程で熱を加えても、変色が少ない塩化ビュル系 繊維を提供できることを見出して本発明を完成するに至った。 The inventors of the present invention investigated the cause of the above problems: 1) The vinyl resin composition containing the above-mentioned "hydrite-talcite-based heat stabilizer" The fact that carbides of chloride-based resins are clogged in a wire mesh in a melt-spinning machine during melt spinning using a melt spinning machine, and 2) vinyl chloride containing the above-mentioned "hydrite-talcite-based heat stabilizer" as a component When heat is applied to the base fiber to cause curling, the problem of discoloration of the salt-bullet base fiber is It has been found that it is caused by the poor dispersion of the id mouth talcite heat stabilizer. The inventors of the present invention have, based on strong findings, (a) 100 parts by mass of a salt-based grease, and (b) a heat stabilizer based on an id-portal talc 0.2-5. When (c) epoxy compound 0.2.10-10.0 parts by mass was added to the vinyl chloride-based resin composition containing 0 parts by mass, a hydride-talcite-based heat stabilizer was used. Also, it has been found that long-run properties of melt spinning can be secured, good and stable productivity can be obtained, and moreover, it is possible to provide a chloride-based fiber with less discoloration even if heat is applied in the curling step. It came to complete.
[0010] 即ち、請求項 1に記載された発明は、前記目的を達成するために、(a)塩ィ匕ビュル 系榭脂 100質量部、(b)ハイド口タルサイト系熱安定剤 0. 2-5. 0質量部、及び、 (c )エポキシ化合物 0. 2— 10. 0質量部を含有する塩化ビニル系榭脂組成物で構成さ れていることを特徴とする塩ィ匕ビュル系繊維である。  That is, in order to achieve the above object, according to the invention described in claim 1, (a) 100 parts by mass of a salt-based resin, (b) a hydite-talcite-based heat stabilizer 0. A vinyl chloride resin composition comprising 2 to 5 parts by mass and (c) an epoxy compound 0.2 to 10.0 parts by mass; It is a fiber.
[0011] 請求項 2に記載された発明は、請求項 1に記載された発明において、前記エポキシ 化合物が、エポキシィ匕大豆油、エポキシ化亜麻仁油、エポキシィ匕桐油、エポキシィ匕 魚油、エポキシィ匕牛脂油、エポキシィ匕ひまし油、エポキシィ匕サフラワー油等のェポキ シ化動植物油、エポキシ含有メタクリル酸ィ匕合物、エポキシ化ステアリン酸メチル、ェ ポキシィ匕ポリブタジエン、トリス(エポキシプロピル)イソシァヌレート、エポキシィ匕トー ル油脂肪酸エステル、エポキシ化亜麻仁油脂肪酸エステル、ビニルクロへキセンジ ェポキサイド、ジシクロへキセンカルボキシレート、ビスフエノール Aジグリシジルエー テル、グリセリンポリグリシジルエーテル、及び、シクロへキサンジメタノールポリグリシ ジルエーテル力 選ばれる少なくとも一種のエポキシィ匕合物であることを特徴とする ものである。  [0011] The invention described in claim 2 relates to the invention described in claim 1, wherein the epoxy compound is an epoxy-based soybean oil, an epoxidized linseed oil, an epoxy-based soybean oil, an epoxy-based fish oil, an epoxy-based beef oil. Epoxy oil, castor oil, epoxy oil, safflower oil, etc. Epoxidized animal and animal oils, epoxy-containing methacrylic acid compounds, epoxidized methyl stearate, epoxy butadiene polybutadiene, tris (epoxypropyl) isocyanurate, epoxy oil Fatty acid ester, epoxidized linseed oil fatty acid ester, vinyl chlorohexene epoxide, dicyclohexene carboxylate, bisphenol A diglycidyl ether, glycerin polyglycidyl ether, and cyclohexane dimethanol polyglycidyl ether power It is characterized in that at least one of Epokishii 匕合 thereof.
[0012] 請求項 3に記載された発明は、請求項 1又は 2に記載された発明において、前記塩 化ビュル系榭脂組成物が、さらに、(d)窒素含有ポリオール 0. 01-2. 0質量部を含 有することを特徴とするものである。  [0012] The invention described in claim 3 relates to the invention described in claim 1 or 2, wherein the chlorinated boule-based resin composition further comprises (d) a nitrogen-containing polyol 0. 01-2. It is characterized in that it contains 0 parts by mass.
[0013] 請求項 4に記載された発明は、請求項 3に記載された発明において、前記窒素含 有ポリオールが、トリス(2—ヒドロキシェチル)イソシァヌレート、トリス(3—ヒドロキシプロ ピル)イソシァヌレート、又は、トリス(4ーヒドロキシブチル)イソシァヌレートであることを 特徴とするものである。 [0014] 請求項 5に記載された発明は、(a)塩ィ匕ビュル系榭脂 100質量部、(b)ハイド口タル サイト系熱安定剤 0. 2-5. 0質量部、及び、(c)エポキシィ匕合物 0. 2— 10. 0質量 部を含有する塩ィ匕ビュル系榭脂組成物を 170— 190°Cの温度で溶融紡糸すること を特徴とするものである。 [0013] The invention described in claim 4 relates to the invention described in claim 3, wherein the nitrogen-containing polyol is tris (2-hydroxyethyl) isocyanurate, tris (3-hydroxy propyl) isocyanurate, Alternatively, it is characterized by being tris (4-hydroxybutyl) isocyanurate. [0014] The invention described in claim 5 is as follows: (a) 100 parts by mass of a salt-and-bure based resin, (b) a hydifice-based thermal stabilizer 0.2-5. 0 parts by mass, and (C) Epoxy compound: A salt-based resin composition containing 0.2 to 10.0 parts by mass is melt-spun at a temperature of 170 to 190 ° C.
[0015] 請求項 6に記載された発明は、請求項 5に記載された発明において、前記溶融紡 糸した塩ィ匕ビュル系繊維を 90— 120°Cの温度に保持した空気雰囲気下で 2— 4倍 まで延伸した後、この延伸した塩ィ匕ビュル系繊維を 110— 140°Cの温度に保持した 空気雰囲気下で延伸した繊維の繊維長の 60— 100%の長さに収縮するまで熱弛緩 させることを特徴とするちのである。  [0015] The invention described in claim 6 is the method according to the invention described in claim 5, under the atmosphere of air in which the melt spun chloride-based boule fiber is maintained at a temperature of 90-120 ° C. — After being drawn to 4 times, this drawn chloride-based fiber is kept at a temperature of 110-140 ° C. until it shrinks to a length of 60-100% of the fiber length of the drawn fiber under an air atmosphere It is characterized by heat relaxation.
[0016] 請求項 7に記載された発明は、請求項 5又は 6に記載された発明において、前記塩 化ビュル系榭脂組成物が、さらに、(d)窒素含有ポリオール 0. 01-2. 0質量部を含 有することを特徴とするものである。  [0016] In the invention described in claim 7, in the invention described in claim 5 or 6, the chlorinated boule-based resin composition further comprises (d) a nitrogen-containing polyol 0. 01-2. It is characterized in that it contains 0 parts by mass.
発明の効果  Effect of the invention
[0017] 請求項 1, 2に記載された発明によれば、(a)塩ィ匕ビ二ル系榭脂 100質量部、(b)ハ イド口タルサイト系熱安定剤 0. 2-5. 0質量部、及び、(c)エポキシ化合物 0. 2— 10 . 0質量部を含有する塩化ビニル系榭脂組成物で構成されているので、ハイド口タル サイト系熱安定剤を使用しても、溶融紡糸のロングラン性が確保されて、良好で安定 した生産性が得られ、しカゝも、カール付与工程で熱を加えても、変色が少ない塩ィ匕ビ -ル系繊維を提供することができる。  According to the invention as recited in claims 1 and 2, (a) 100 parts by mass of a vinyl-based resin, (b) a heat-portal thermal stabilizer 0.2-5 Since it is composed of a vinyl chloride resin composition containing 0 parts by mass and (c) an epoxy compound 0.2 to 10.0 parts by mass, a hydite talcite-based heat stabilizer is used Also, long runnability of melt spinning is secured, and good and stable productivity is obtained, and salty vinyl fiber with less discoloration even if heat is applied in the curling process is provided. can do.
[0018] 請求項 3, 4に記載された発明によれば、前記塩ィ匕ビ二ル系榭脂組成物が、さらに 、(d)窒素含有ポリオール 0. 01-2. 0質量部を有しているので、前記エポキシィ匕合 物との相乗効果によって、カール付与工程で熱をカ卩えた際の変色の抑制効果を 、つ そう向上させることができる。  [0018] According to the invention as recited in claims 3 and 4, the vinyl chloride resin composition further comprises (d) a nitrogen-containing polyol in an amount of 0.1-2 parts by mass. Because of the synergistic effect with the epoxy compound, the effect of suppressing color change when heat is applied in the curling step can be improved.
[0019] 請求項 5, 6に記載された発明によれば、(a)塩ィ匕ビ二ル系榭脂 100質量部、(b)ハ イド口タルサイト系熱安定剤 0. 2-5. 0質量部、及び、(c)エポキシ化合物 0. 2— 10 . 0質量部を含有する塩化ビュル系榭脂組成物を 170— 190°Cの温度で溶融紡糸 するので、ハイド口タルサイト系熱安定剤を使用しても、溶融紡糸のロングラン性が確 保されて、良好で安定した生産性が得られ、しカゝも、カール付与工程で熱を加えても 、変色が少な!/ヽ塩ィ匕ビュル系繊維を提供することができる。 [0019] According to the invention described in claims 5 and 6, (a) 100 parts by mass of a vinyl chloride resin, (b) a thermal stabilizer based on a hyaluronan-based material 0.2-5 Hydride-talcite-based resin composition is melt-spinned at a temperature of 170-190 ° C. by using a chloride-based resin composition containing 0 parts by mass and (c) an epoxy compound of 0.2 to 10 parts by mass. Even if a heat stabilizer is used, the long-run property of melt spinning is ensured, and good and stable productivity is obtained, and even if heat is applied in the curling step, the kneader is also used. Low discoloration! / ヽ 匕 系 fiber can be provided.
[0020] 請求項 7に記載された発明によれば、前記塩ィ匕ビ二ル系榭脂組成物が、さらに、(d )窒素含有ポリオール 0. 01-2. 0質量部を有しているので、前記エポキシ化合物と の相乗効果によって、カール付与工程で熱をカ卩えた際の変色の抑制効果を!、つそう 向上させることができる。 [0020] According to the invention described in claim 7, the vinyl chloride resin composition further comprises (d) 0.1 to 20 parts by mass of a nitrogen-containing polyol. Because of the synergistic effect with the epoxy compound, the effect of suppressing discoloration when heat is applied in the curling step can be improved.
発明を実施するための最良の形態  BEST MODE FOR CARRYING OUT THE INVENTION
[0021] 本発明の塩ィ匕ビニル系繊維は、(a)塩ィ匕ビ二ル系榭脂 100質量部、(b)ハイドロタ ルサイト系熱安定剤 0. 2-5. 0質量部、及び、(c)エポキシ化合物 0. 2— 10. 0質 量部を含有する塩化ビニル系榭脂組成物で構成されている。  [0021] The vinyl chloride-based fiber of the present invention comprises (a) 100 parts by mass of a vinyl chloride-based resin, (b) a thermal stabilizer based on hydrotalcite, and 0.5 to 2.0 parts by mass, (C) Epoxy compound It is composed of a vinyl chloride resin composition containing 0.2 to 10.0 parts by mass.
[0022] このように、 (a)塩ィ匕ビ二ル系榭脂 100質量部、及び、(b)ハイド口タルサイト系熱安 定剤 0. 2-5. 0質量部を含有する塩化ビュル系榭脂組成物に、(c)エポキシ化合 物 0. 2— 10. 0質量部を含有させると、ノ、イド口タルサイト系熱安定剤を使用しても、 溶融紡糸のロングラン性が確保されて、良好で安定した生産性が得られ、し力も、力 ール付与工程で熱を加えても、変色が少な ヽ塩ィ匕ビュル系繊維を提供することがで きる。  Thus, (a) 100 parts by mass of a vinyl chloride-based resin and (b) a hydrotalcite-based heat stabilizer 0.2 to 50 parts by mass When (b) epoxy compound 0.2.10 parts by mass is added to the boule-based resin composition, the long-run property of melt spinning is improved even when using a nodite-talcite-based heat stabilizer. As a result, good and stable productivity can be obtained, and even if heat is applied in the force application step, it is possible to provide a salt-free fiber with little discoloration.
[0023] 前記「塩ィ匕ビ二ル系榭脂」は、(ィ)塩ィ匕ビニルの塊状重合、溶液重合、懸濁重合、 乳化重合等によって得られたものであるが、その重合方法には特に限定されず、例 えば、ポリ塩化ビニル、塩素化ポリ塩ィ匕ビニル、ポリ塩ィ匕ビユリデン、塩素化ポリェチ レン、塩ィ匕ビ二ルー酢酸ビュル共重合体、塩ィ匕ビ二ルーエチレン共重合体、塩化ビ- ループロピレン共重合体、塩化ビュル スチレン共重合体、塩化ビュル イソブチレン 共重合体、塩ィ匕ビュル一塩ィ匕ビユリデン共重合体、塩ィ匕ビ二ルースチレン 無水マレ イン酸三元共重合体、塩ィ匕ビュル スチレン アクリロニトリル三元共重合体、塩ィ匕ビ 二ルーブタジエン共重合体、塩ィ匕ビュル イソプレン共重合体、塩化ビニルー塩素化 プロピレン共重合体、塩ィヒビ二ルー塩ィヒビユリデンー酢酸ビュル三元共重合体、塩ィ匕 ビュル マレイン酸エステル共重合体、塩ィ匕ビュルーメタクリル酸エステル共重合体、 塩ィ匕ビュル アクリロニトリル共重合体、塩ィ匕ビ二ルー各種ビュルエーテル共重合体 等の塩素含有榭脂、(口)それらの相互のブレンド品、(ハ)それらの塩素含有樹脂と 他の塩素を含まない合成樹脂、例えば、アクリロニトリル スチレン共重合体、アタリ口 二トリルースチレン ブタジエン三元共重合体、エチレン 酢酸ビニル共重合体、ェチ レンーェチル (メタ)アタリレート共重合体、ポリエステル等とのブレンド品、或いは、(二[0023] The above-mentioned "vinyl chloride-based resin" is obtained by bulk polymerization, solution polymerization, suspension polymerization, emulsion polymerization and the like of (i) vinyl chloride, and the polymerization method thereof For example, polyvinyl chloride, chlorinated polyvinyl chloride, polyvinyl chloride, polyvinyl chloride, chlorinated polyethylene, chloride-vinyl acetate copolymer, chloride-vinyl chloride, and the like. Ruethylene copolymer, vinyl chloride-propylene copolymer, butyl chloride-styrene copolymer, chloride-bullet isobutylene copolymer, chloride-polyether-biarylidene copolymer, chloride-bistyrene copolymer, anhydrous Maleic acid terpolymers, vinyl styrene-acrylonitrile terpolymers, vinyl chloride-butadiene copolymers, vinyl isoprene copolymers, vinyl chloride-chlorinated propylene copolymers, Shiojibi-bi -Salt byluriden acetate-Bullet acetate terpolymer, Chloride burl-Maleic ester copolymer, Chloride-Bryl methacrylate ester copolymer, Chloride-Bryl-Acrylonitrile copolymer, Chloride-Bivinyl various Chlorine-containing resins such as boule ether copolymers, (the mouth) blends of them with each other, (iii) those chlorine-containing resins and other chlorine-free synthetic resins, such as acrylonitrile styrene copolymer, atari mouth Blends with ditrilostyrene-butadiene terpolymer, ethylene-vinyl acetate copolymer, ethylene-ethyl (meth) atarylate copolymer, polyester, etc., or
)塩化ビュルを重合含有するブロック共重合体、塩ィヒビュルを重合含有するグラフト 共重合体等をあげることができる。 And the like) block copolymers which contain chloride chloride, and graft copolymers which contain sodium chloride.
[0024] 前記「繊維用塩ィ匕ビ二ル系榭脂組成物」には、従来塩ィ匕ビニル系組成物に使用さ れる公知の添加剤を配合してもよい。これらの添加剤は、例えば、可塑剤、滑剤、相 溶化剤、加工助剤、強化剤、紫外線吸収剤、酸化防止剤、帯電防止剤、充填剤、難 燃剤、顔料、初期着色改善剤、導電性付与剤、表面処理剤、光安定剤、及び、香料 である。  [0024] The above-mentioned "salt-based vinyl fat composition for fibers" may be blended with known additives used in conventional salt-vinyl based compositions. These additives include, for example, plasticizers, lubricants, compatibilizers, processing aids, toughening agents, UV absorbers, antioxidants, antistatic agents, fillers, flame retardants, pigments, initial color improvers, conductive agents. Gendering agents, surface treatment agents, light stabilizers, and perfumes.
[0025] 本発明の塩化ビュル系繊維は、その一本の太さ力 好ましくは, 20— 100デニー ルであり、さらに好ましくは、 50— 80デニールである。このように、塩化ビュル繊維一 本の太さが 20— 100デニールであると、天然の毛髪と遜色がないものとなり、そして 、塩ィ匕ビュル繊維一本の太さが 50— 80デニールであると、それにカ卩えて、触感及び 風合いが向上したものとなる。  [0025] The chlorine burle-based fiber of the present invention preferably has a thickness of 20 to 100 denier, more preferably 50 to 80 denier. Thus, if the thickness of one chloride burle fiber is 20 to 100 denier, it becomes comparable to natural hair, and if the thickness of one chloride boule fiber is 50 to 80 denier In addition, the touch and feel are improved.
[0026] 本発明の塩化ビニル系繊維の断面形状は、いかなるものでもよぐ例えば、円形、 楕円形、メガネ形、星形、 H字形、丁字形、 Y字形、三角形、四角形、十字形、ハート 形、馬蹄形、又は、これらの組み合わせでもよい。また、これらの中空体であってもよ い。  The cross-sectional shape of the vinyl chloride-based fiber of the present invention may be any shape, for example, circular, oval, glasses, star, H-shaped, double-sided, Y-shaped, triangle, square, cross, heart It may be a shape, a horseshoe shape, or a combination of these. Also, these hollow bodies may be used.
[0027] 本発明における「ノヽイド口タルサイト系熱安定剤」は、有機スズ系熱安定剤のように 、環境における微生物に悪影響をおぼしたり、臭気を発生させるといった問題がなく 、し力も、毒性がない。このような「ノヽイド口タルサイト系熱安定剤」は、具体的には、ハ イド口タルサイトイ匕合物であり、さらに具体的には、マグネシウム及び z又はアルカリ 金属とアルミニウム或いは亜鉛、マグネシウム及びアルミニウム力もなる複合塩ィ匕合 物である。また、それらの複合塩には、化合物結晶水を脱水したものもある。また、ハ イド口タルサイト化合物は、天然物であっても合成品であってもよいが、合成品の合成 方法としては、従来公知の方法でよい。  [0027] The "noid-in-mouth-talcite-based heat stabilizer" in the present invention does not have the problem of adversely affecting the microorganisms in the environment or generating an odor like the organotin-based heat stabilizer, There is no toxicity. Specifically, such "noid-opening-talcite-based heat stabilizers" are compounds with a light-opening-talcite compound, and more specifically, magnesium and z or an alkali metal and aluminum, zinc, magnesium, or magnesium. It is a composite salt compound that also has aluminum power. In addition, some of their complex salts are those obtained by dehydrating the compound crystal water. In addition, the high mouth talcite compound may be a natural product or a synthetic product, but as a synthetic method of the synthetic product, a conventionally known method may be used.
[0028] 本発明においては、前記ノ、イド口タルサイト系熱安定剤の配合量が 0. 2質量部より 少ないと、糸切れ頻度が増加し、そして、前記ノ、イド口タルサイト系熱安定剤の配合 量が 5. 0質量部より多いと、初期着色性を悪化させるる。したがって、本発明におい ては、前記ハイド口タルサイト系熱安定剤の配合量は、好ましくは、 0. 2-5. 0質量 部であり、さらに好ましくは、 0. 5-3. 0質量部である。 In the present invention, the yarn breakage frequency increases when the blending amount of the gauze and lidoguchi heat-site-based heat stabilizer is less than 0.2 parts by mass, and the gauze and i-domouth talcite-based heat resistance Stabilizer formulation If the amount is more than 5.0 parts by mass, the initial colorability is deteriorated. Therefore, in the present invention, the blending amount of the above-mentioned hyd- ide-talcite-based heat stabilizer is preferably 0.2-5. 0 parts by mass, and more preferably 0.5-5. 0 parts by mass. It is.
[0029] 本発明における「エポキシィ匕合物」は、好ましくは、エポキシィ匕大豆油、エポキシィ匕 亜麻仁油、エポキシィ匕桐油、エポキシ化魚油、エポキシィ匕牛脂油、エポキシィ匕ひまし 油、エポキシィ匕サフラワー油等のエポキシィ匕動植物油、エポキシ含有メタクリル酸ィ匕 合物、エポキシ化ステアリン酸メチル、エポキシ化ポリブタジエン、トリス(エポキシプロ ピル)イソシァヌレート、エポキシ化トール油脂肪酸エステル、エポキシ化亜麻仁油脂 肪酸エステル、ビュルクロへキセンジェポキサイド、ジシクロへキセンカルボキシレー ト、ビスフエノール Aジグリシジルエーテル、グリセリンポリグリシジルエーテル、及び、 シクロへキサンジメタノールポリグリシジルエーテルから選ばれる少なくとも一種のェ ポキシ化合物であるが、本発明の目的に反しない限りこれらのエポキシィ匕合物以外 のエポキシ化合物であっても力まわな 、。 [0029] The "epoxy compound" in the present invention is preferably epoxy soybean oil, epoxy soybean linseed oil, epoxy soybean oil, epoxidized fish oil, epoxy oil calf oil, epoxy oil castor oil, epoxy oil safflower Epoxides and oils such as oil and vegetable oils, epoxy-containing methacrylic acid compounds, epoxidized methyl stearate, epoxidized polybutadiene, tris (epoxypropyl) isocyanurate, epoxidized tall oil fatty acid ester, epoxidized linseed oil fatty acid ester, And at least one epoxy compound selected from biphenyl hexahexene, dicyclohexene carboxylate, bisphenol A diglycidyl ether, glycerin polyglycidyl ether, and cyclohexane dimethanol polyglycidyl ether. That is, as long as it 's Chikarama be epoxy compounds other than these Epokishii 匕合 thereof it is not contradictory to the object of the present invention.
[0030] 本発明においては、前記「エポキシィ匕合物」の配合量が 0. 2質量部より少ないと、 溶融紡糸のロングラン性の改善効果や製造される塩ィ匕ビニル系繊維の変色抑制効 果が小さくなり、そして、前記エポキシィ匕合物の配合量が 10. 0質量部より多いと、糸 切れ頻度が増加する。したがって、本発明においては、前記エポキシィ匕合物の配合 量は、好ましくは、 0. 2— 10. 0質量部であり、さらに好ましくは、 0. 5-3. 0質量部 である。  In the present invention, when the compounding amount of the “epoxy compound” is less than 0.2 parts by mass, the effect of improving the long-run property of melt spinning or the color change suppressing effect of the vinyl chloride fiber produced can be improved. The fruit becomes smaller, and when the blending amount of the epoxy compound is more than 10.0 parts by mass, the frequency of thread breakage increases. Therefore, in the present invention, the compounding amount of the epoxy compound is preferably 0.2 to 10.0 parts by mass, more preferably 0.5 to 30.0 parts by mass.
[0031] 本発明にお 、ては、前記塩ィ匕ビュル系榭脂組成物は、好ましくは、さらに、(d)窒 素含有ポリオール 0. 01-2. 0質量部を含有することができる。このように前記塩ィ匕 ビュル系榭脂組成物力 さらに、(d)窒素含有ポリオール 0. 01-2. 0質量部を有し ていると、前記エポキシィ匕合物との相乗効果によって、カール付与工程で熱をカ卩えた 際の変色の抑制効果を 、つそう向上させることができる。  In the present invention, preferably, the salt-and-brull-based resin composition may further contain (d) 0.1 to 20 parts by mass of a nitrogen-containing polyol. . Thus, when the salt-like resin composition power is further added, (d) a nitrogen-containing polyol in an amount of 0.1 to 2 parts by mass, curling is imparted due to the synergistic effect with the epoxy compound. The effect of suppressing color change when heat is applied in the process can be greatly improved.
[0032] 前記窒素含有ポリオールは、好ましくは,トリス(2—ヒドロキシェチル)イソシァヌレー ト、トリス(3—ヒドロキシプロピル)イソシァヌレート、又は、トリス (4ーヒドロキシブチノレ)ィ ソシァヌレートである力 本発明の目的に反しない限りこれらの窒素含有ポリオール 以外のエポキシ化合物であっても力まわな 、。 [0033] 本発明においては、前記窒素含有ポリオールの配合量が 0. 01質量部より少ないと 、カール付与工程で熱を加えた際の変色を少なくする効果力 、さくなり、そして、前 記窒素含有ポリオールの配合量が 2. 0質量部より多いと糸切れ頻度が増加する。し たがって、本発明においては、前記窒素含有ポリオールの配合量は、好ましくは、 0. 01-2. 0質量部であり、さらに好ましくは、 0. 02-1. 0質量部である。 [0032] The nitrogen-containing polyol is preferably tris (2-hydroxyethyl) isocyanurate, tris (3-hydroxypropyl) isocyanurate, or tris (4-hydroxybutynore) isocyanurate. Even if it is an epoxy compound other than these nitrogen-containing polyols, unless it is against the purpose. In the present invention, if the blending amount of the nitrogen-containing polyol is less than 0.01 parts by mass, the effect of reducing the color change when heat is applied in the curling step becomes poor, and the nitrogen If the blending amount of the contained polyol is more than 2.0 parts by mass, the yarn breakage frequency is increased. Therefore, in the present invention, the blending amount of the nitrogen-containing polyol is preferably 0.01 to 2.0 parts by mass, and more preferably 0.02 to 1.0 parts by mass.
[0034] 本発明の塩ィ匕ビニル系繊維は、好ましくは、(a)塩ィ匕ビ二ル系榭脂 100質量部、(b )ハイド口タルサイト系熱安定剤 0. 2-5. 0質量部、及び、(c)エポキシィ匕合物 0. 2 一 10. 0質量部を含有する塩ィ匕ビ二ル系榭脂組成物を 170— 190°Cの温度で溶融 紡糸することにより製造される。このように、 (a)塩ィ匕ビ二ル系榭脂 100質量部、(b)ハ イド口タルサイト系熱安定剤 0. 2-5. 0質量部、及び、(c)エポキシ化合物 0. 2— 10 . 0質量部を含有する塩化ビュル系榭脂組成物を 170— 190°Cの温度で溶融紡糸 すると、ハイド口タルサイト系熱安定剤を使用しても、溶融紡糸のロングラン性が確保 されて、良好で安定した生産性が得られ、しカゝも、カール付与工程で熱を加えても、 変色が少ない塩ィ匕ビュル系繊維を提供することができる。  [0034] The vinyl chloride-based fiber of the present invention is preferably (a) 100 parts by mass of vinyl chloride-based resin, (b) thermal stabilizer based on hyde-portal talc 0.2-5. By melt spinning a vinyl chloride resin composition containing 0 parts by mass and (c) 0.20 parts by mass of epoxy compound at a temperature of 170 to 190 ° C. Manufactured. Thus, (a) 100 parts by mass of vinyl chloride resin, (b) thermal stabilizer based on 0.52 parts by mass of a talc-based heat stabilizer, and (c) epoxy compound 0 Melt-spinning of a chloride-based resin composition containing 2 to 10 parts by mass at a temperature of 170 to 190 ° C. ensures long-run properties of melt-spinning even with the use of a hydrotalcite-based heat stabilizer. As a result, good and stable productivity can be obtained, and even if heat is applied in the curling step, it is possible to provide a salt-like fiber with little discoloration.
[0035] 本発明の塩ィ匕ビニル系繊維の製造にぉ ヽては、前記「塩化ビニル系榭脂組成物」 をヘンシェルミキサ、リボンプレンダ等の混合機を使用して混合したパウダーコンパゥ ンド、又は、これを溶融混合したペレットコンパゥンドを、単軸押出機、異方向二軸押 出機、コ-カルニ軸押出機等の溶融押出機を使用して 170— 190°Cの温度で溶融 紡糸することにより製造される。  [0035] For producing the vinyl chloride-based fiber of the present invention, a powder compound is prepared by mixing the above-mentioned "vinyl chloride resin composition" using a mixer such as a Henschel mixer, a ribbon platen, etc., Alternatively, a pellet compound obtained by melt-mixing the same is melted at a temperature of 170-190 ° C. using a melt extruder such as a single-screw extruder, a counter-rotating twin-screw extruder, or a co-Carni shaft extruder. It is manufactured by spinning.
[0036] 本発明の塩ィ匕ビニル系繊維の製造においては、前記溶融紡糸した塩化ビニル系 繊維を 90— 120°Cの温度に保持した空気雰囲気下で 2— 4倍まで延伸した後、この 延伸した塩化ビニル系繊維を 110— 140°Cの温度に保持した空気雰囲気下で処理 前の 60— 100%の長さになるまで熱弛緩させる。  In the production of the vinyl chloride-based fiber of the present invention, the melt-spun vinyl chloride-based fiber is stretched to 2 to 4 times in an air atmosphere maintained at a temperature of 90 to 120 ° C. The drawn vinyl chloride fiber is thermally relaxed in an air atmosphere maintained at a temperature of 110-140 ° C. to a length of 60-100% before treatment.
[0037] 本発明の塩ィ匕ビニル系繊維の製造にぉ ヽては、前記塩化ビュル系榭脂組成物は 、好ましくは、さらに、(d)窒素含有ポリオール 0. 01-2. 0質量部を含有させることが できる。このように、前記塩ィ匕ビ二ル系榭脂組成物力 さらに、(d)窒素含有ポリオ一 ル 0. 01-2. 0質量部を有していると、前記エポキシィ匕合物との相乗効果によって、 カール付与工程で熱を加えた際の変色の抑制効果をいつそう向上させることができ る。 In order to produce the vinyl chloride-based fiber of the present invention, preferably, the chloride-based resin composition preferably further includes (d) a nitrogen-containing polyol of 0.1 to 20 parts by mass. Can be contained. Thus, when the salt-to-water vinyl-based resin composition further has (d) nitrogen-containing polyol 0.1 to 20 parts by mass, the synergy with the epoxy compound is obtained. By the effect, it is possible to improve the suppression effect of color change when heat is applied in the curling process. Ru.
実施例  Example
[0038] (実施例 1)  Example 1
(a)塩ィ匕ビニル榭脂 (大洋塩ビ株式会社製、 TH— 1000) 80質量部と、塩素化塩化 ビニル榭脂 (積水化学工業株式会社製、 HA— 24K) 10質量部と、エチレン'酢ビ Ζ 塩ビグラフト重合榭脂 (積水化学工業株式会社製、 TGH-1100) 10質量部とを配合 して得た塩ィ匕ビ二ル系榭脂 100質量部、(b)ハイド口タルサイト系熱安定剤 (協和化 学社製、アル力マイザ一— 1) 2質量部、(c)エポキシィ匕合物(日本油脂社製、フアル ノック 75ASV) 0. 8質量部、(d)窒素含有のポリオール(日産化学社製、 NF-SE)0 . 5質量部、(e)亜リン酸エステルイ匕合物 (旭電ィ匕社製、アデカスタブ PEP— 8) 0. 5質 量部、(f)亜鉛石鹼(日産化学社製 NF— 12Zn) 0. 8質量部、(g)カルシウム石鹼(日 産化学社製、 NF-12Ca) l. 0質量部、及び、(h)エステル系滑剤(理研ビタミン社 製 EW-100) 0. 7質量部を含有する塩化ビニル系榭脂組成物を、ノズル断面積 0. 06mm2、孔数 120、及び,金型温度 175°Cの紡糸金型から、押出量 lOKgZ時間 で溶融紡糸して、平均繊度 135デニールの塩ィ匕ビュル系繊維とした。そして、この塩 化ビュル系繊維を 105°Cの空気雰囲気下で 300%まで延伸した後、この延伸した繊 維を、 110°Cの空気雰囲気下で、延伸した繊維の繊維長の 75%の長さに収縮する まで、熱弛緩させて平均繊度 60デニールの塩ィ匕ビュル系繊維を得た。 (a) 80 parts by mass of vinyl chloride vinyl chloride (manufactured by Taiyo U.S. Chloride, TH-1000) and 10 parts by mass of chlorinated vinyl chloride resin (manufactured by Sekisui Chemical Co., Ltd., HA-24K) and ethylene ' 100 parts by mass of a vinyl chloride resin obtained by blending 10 parts by mass of vinyl acetate / vinyl chloride / vinyl graft polymer resin (manufactured by Sekisui Chemical Co., Ltd., TGH-1100) Heat stabilizer (Kyoto Chemical Co., Ltd., Almizer 1) 2 parts by mass, (c) Epoxy compound (Nippon Yushi Co., Ltd., Falknock 75 ASV) 0.8 part by mass, (d) nitrogen-containing Polyol (Nissan Chemical Co., Ltd., NF-SE): 0.5 parts by mass, (e) phosphite ester compound (Asaken Denshi Co., Ltd., Adekastab PEP-8) 0.5 mass part, (f ) 0.8 part by weight of zinc stone (NF-12 Zn manufactured by Nissan Chemical Co., Ltd.), 1.0 part by weight of calcium stone (NF-12Ca made by Nissei Chemical Co., Ltd.), and (h) ester-based lubricant (Manufactured by Riken Vitamin Co., Ltd. EW-100) 0. 7 parts by mass Vinyl chloride榭脂compositions containing, the nozzle cross-sectional area 0. 06mm 2, hole number 120, and, from a spinning die mold temperature 175 ° C, was melt-spun at an extrusion amount lOKgZ time, average fineness 135 It is a denier's salted fiber-based fiber. Then, after the chlorinated boule fiber is drawn to 300% in an air atmosphere at 105 ° C., the drawn fiber is taken to 75% of the fiber length of the drawn fiber in an air atmosphere at 110 ° C. It was heat-relaxed until it shrunk to a length to obtain a salted boule fiber having an average fineness of 60 denier.
[0039] (実施例 2)  Example 2
塩ィ匕ビュル系榭脂組成物に、(d)窒素含有のポリオール (日産化学社製、 NF-SE) 0. 5質量部を含有させな力つた以外は、前記実施例 1と同様にして塩ィ匕ビ二ル系繊 維を得た。  The same procedure as in Example 1 was repeated except that 0.5 parts by mass of (d) nitrogen-containing polyol (NF-SE, manufactured by Nissan Chemical Co., Ltd.) was added to the salt-bure based resin composition. A salt-based fiber was obtained.
[0040] (実施例 3)  (Example 3)
塩ィ匕ビュル系榭脂組成物に、(d)窒素含有のポリオール (日産化学社製、 NF-SE) 5質量部を含有させた以外は、前記実施例 1と同様にして塩ィ匕ビュル系繊維を得た。  Example 1 was repeated except that 5 parts by mass of (d) nitrogen-containing polyol (NF-SE, manufactured by Nissan Chemical Co., Ltd.) was added to the salt-to-bule type resin composition in the same manner as in Example 1 above. System fiber was obtained.
[0041] (比較例 1)  Comparative Example 1
(a)塩ィ匕ビニル榭脂 (大洋塩ビ株式会社製、 TH— 1000) 80質量部と、塩素化塩化 ビニル榭脂 (積水化学工業株式会社製、 HA— 24K) 10質量部と、エチレン'酢ビ Ζ 塩ビグラフト重合榭脂 (積水化学工業株式会社製、 TGH-1100) 10質量部とを配合 して得た塩ィ匕ビ二ル系榭脂 100質量部、(b)ハイド口タルサイト系熱安定剤 (協和化 学社製、アル力マイザ一— 1) 0. 1質量部、(c)エポキシィ匕合物(日本油脂社製、ファ ルパック 75ASV) 0. 8質量部、(e)亜リン酸エステルイ匕合物 (旭電ィ匕社製、アデカス タブ PEP-8) 0. 5質量部、(f)亜鉛石鹼(日産化学社製 NF-12Zn) 0. 8質量部、(g )カルシウム石鹼(日産化学社製、 NF-12Ca) 1. 0質量部、及び、(h)エステル系滑 剤 (理研ビタミン社製 EW-100) 0. 7質量部を含有する塩化ビニル系榭脂組成物を 、ノズル断面積 0. 06mm2、孔数 120、及び,金型温度 175°Cの紡糸金型から、押 出量 lOKgZ時間で溶融紡糸して、平均繊度 135デニールの塩ィ匕ビニル系繊維とし た。そして、この塩化ビュル系繊維を 105°Cの空気雰囲気下で 300%まで延伸した 後、この延伸した繊維を、 110°Cの空気雰囲気下で、延伸した繊維の繊維長の 75% の長さに収縮するまで、熱弛緩させて平均繊度 60デニールの塩ィ匕ビニル系繊維を 得た。 (a) 80 parts by mass of vinyl chloride vinyl chloride (manufactured by Taiyo U.S. Chloride, TH-1000) and 10 parts by mass of chlorinated vinyl chloride resin (manufactured by Sekisui Chemical Co., Ltd., HA-24K) and ethylene ' Sweet potato vinegar 100 parts by weight of vinyl chloride resin obtained by blending 10 parts by weight of vinyl chloride graft resin (TGH-1100, manufactured by Sekisui Chemical Co., Ltd.) Agent (Kyoto Chemical Co., Ltd., Almighty Mizer 1) 0.1 part by mass, (c) Epoxy compound (FALPACK 75 ASV manufactured by NOF Corporation) 0.8 part by mass, (e) phosphorous acid Ester compound (Asahi Den IC Co., Ltd., Adekas tub PEP-8) 0.5 part by mass, (f) Zinc stone crucible (Nissan Chemical Co., Ltd. NF-12 Zn) 0.8 part by mass, (g) calcium stone Vinyl chloride-based resin composition containing 1.0 part by mass of 鹼 (Nissan Chemical Co., Ltd., NF-12Ca), and 0.7 part by mass of (h) ester-based lubricant (EW-100 manufactured by Riken Vitamin Co., Ltd.) The melt-spinning was carried out with a nozzle cross-sectional area of 0.06 mm 2 , a hole number of 120, and a mold temperature of 175 ° C. by an extrusion amount of lOKgZ time, and a vinyl chloride fiber of an average fineness of 135 denier. I asked. Then, after the chloride-based fiber is drawn to 300% in an air atmosphere at 105 ° C., this drawn fiber is 75% of the fiber length of the drawn fiber in an air atmosphere at 110 ° C. The mixture was heat-relaxed until it shrunk to give a vinyl chloride-based fiber having an average fineness of 60 denier.
[0042] (比較例 2)  Comparative Example 2
塩ィ匕ビュル系榭脂組成物に、(b)ハイド口タルサイト系熱安定剤 (協和化学社製、 アル力マイザ一— 1) 10質量部を含有させた以外は、前記比較例 1と同様にして塩ィ匕 ビュル系繊維を得た。  Comparative Example 1 and Comparative Example 1 except that (b) Hyde-portal thalcite-based heat stabilizer (Kyoka Chemical Co., Ltd., Al-Forceizer 1) contained 10 parts by mass in the salt-and-bule-based resin composition. A salted boule based fiber was obtained in the same manner.
[0043] (比較例 3)  Comparative Example 3
塩ィ匕ビュル系榭脂組成物に、(b)ハイド口タルサイト系熱安定剤 (協和化学社製、 アル力マイザ一— 1) 2質量部、及び、(c)エポキシ化合物 (日本油脂社製、フアルパッ ク 75ASV) 0. 1質量部を含有させた以外は、前記比較例 1と同様にして塩ィ匕ビニル 系繊維を得た。  (B) 2 parts by mass of (b) hide mouth thalcite-based heat stabilizer (Kyoka Chemical Co., Ltd., Al-Forceizer 1), and (c) epoxy compound (Nippon Yushi Co., Ltd.) A vinyl chloride-based fiber was obtained in the same manner as in Comparative Example 1 except that 0.1 parts by mass of HALFPACK 75 ASV was contained.
[0044] (比較例 4)  Comparative Example 4
塩ィ匕ビュル系榭脂組成物に、(b)ハイド口タルサイト系熱安定剤 (協和化学社製、 アル力マイザ一— 1) 2質量部、及び、(c)エポキシ化合物 (日本油脂社製、フアルパッ ク 75ASV) 20質量部を含有させた以外は、前記比較例 1と同様にして塩ィ匕ビニル系 繊維を得た。  (B) 2 parts by mass of (b) hide mouth thalcite-based heat stabilizer (Kyoka Chemical Co., Ltd., Al-Forceizer 1), and (c) epoxy compound (Nippon Yushi Co., Ltd.) A vinyl chloride-based fiber was obtained in the same manner as in Comparative Example 1 except that 20 parts by mass of HALPACK 75 ASV was contained.
[0045] 以上、実施例 1一 3及び比較例 1一 4で得られた塩ィ匕ビニル系繊維の (ィ)ロングラ ン性、(口)変色性、(ハ)糸切れ頻度、及び、(二)初期着色性を評価した。評価結果 は、次の表 1に示される。 As described above, Example 1-13 and Comparative Example 1-14 of vinyl chloride-based fibers obtained in (4) Longura Colorability, (mouth) discoloration, (ha) yarn breakage frequency, and (ii) initial colorability were evaluated. The evaluation results are shown in Table 1 below.
[表 1]  [table 1]
Figure imgf000012_0001
Figure imgf000012_0001
[0047] 前記 (ィ)における「ロングラン性」は、溶融紡糸時に金網目詰まりにより糸切れが多 発し、金網を交換しなければ製造を行えない状態になるまでの連続溶融紡糸時間を 表したものであり、その評価基準は、次の The “long run property” in the above item (b) represents continuous melt spinning time until a state in which production can not be performed unless the wire mesh is replaced due to frequent occurrence of thread breakage during melt spinning. And the evaluation criteria are
◎:連続溶融紡糸時が 96時間を超えても糸切れの問題がないので、作業性 '生産 性の点でより効果が上ったもの  :: There is no problem of thread breakage even when continuous melt spinning exceeds 96 hours, so that the effect is improved in terms of workability 'productivity'
〇:連続溶融紡糸時間が 96— 48時間でわずかに糸切れが発生する力 ロングラン 製造として問題がないもの、  Good: Continuous melt spinning time 96 to 48 hours Slight breakage occurs. Forced long run No problem for production
X:連続溶融紡糸時間が 48時間未満で多数の糸切れが発生するので、ロングラン 製造として成り立たないもの  X: A long run can not be produced because a large number of thread breakage occurs in less than 48 hours of continuous melt spinning time
とした。  And
[0048] 前記(口)における「変色性」は、カール付与工程の際の変色度合!/、を判断する特 性値である。この「変色性」は、塩ィ匕ビニル系繊維を緊張させた状態で 105°Cのギア オーブン中で 1時間熱処理した後、熱処理前後の塩ィヒビニル系繊維の色を色差計( 倉敷紡績社製、高精度分光測色機 COLOR - 7X)で測色して、熱処理前の b値 (な お、前記 b値は、 JIS Z 8722の条件 bに準拠した照明 '受光条件で測定した値であ る。)を b とし、そして、熱処理後の bを b としたとさ〖こおける〖こ、 b と b との差 A b、 The “discoloring property” in the above (mouth) is a characteristic value for determining the degree of discoloration at the time of the curling step! / ,. This “discoloring property” is a color difference meter (Kurashiki Spinning Co., Ltd.) after heat treatment in a gear oven at 105 ° C. for 1 hour in a state of tensioning vinyl chloride based fibers before and after heat treatment. The b value before heat treatment measured by color measurement with a high-accuracy spectrophotometer COLOR-7X (Here, the b value is the value measured under the light reception condition of 'illumination based on the condition b of JIS Z 8722. B) and b after heat treatment is b, the difference between b and b, A b,
1 2 1 2 1 2 1 2
即ち、 A b=b — b で評価される力 その評価基準は、次の  That is, the force evaluated by A b = b-b The evaluation criterion is
1 2  1 2
® : A b< 0. 5 であって、目視で変色しているかわ力 ないもの  ®: A b <0.5, with no visible discoloration
O : 0. 5≤A b< l. 0 であって、わずかに変色しているが製品として問題のないも の O: 0.5 ≤ A b <1 or 0, slightly discolored but no problem as a product of
X : l. 0≤Ab であって、目視でも変色しているとわ力り不合格であるもの とした。  X: l. 0≤Ab, and if discolored visually, it is considered to be a failure.
[0049] 前記 (ハ)における「糸切れ頻度」は、溶融紡糸を行った際の単糸切れが起きる回 数であるが、 1時間当りの糸切れ頻度(回数 Z時間)に換算して、次の評価基準 ◎ : 0回 であって、ロングラン製造対象製品として全く問題のないもの  [0049] The "thread breakage frequency" in the above (iii) is the number of occurrences of single yarn breakage when melt spinning is carried out, but converted to the yarn breakage frequency per hour (number of times Z hours), The following evaluation criteria ◎: 0 times, no problem as a product for long run production
〇:1一 2回 であって、ロングラン製造対象製品として問題のないもの  ○: 1 and 2 times, and no problem as a product for long run production
X : 3回以上 であって、ロングラン製造対象製品として問題のあるもの  X: 3 or more times and having problems as products for long run production
で評価した。  It evaluated by.
[0050] 前記 (二)における「初期着色性」は、溶融紡糸した直後の糸の色を目視により評価 される力 その評価基準は、次の  The “initial colorability” in the above (2) is the force with which the color of the yarn immediately after melt-spinning is visually evaluated.
〇:黄変がないもの  ○: There is no yellowing
X:黄変があるもの  X: There is yellowing
とした。  And
[0051] 表 1から次のことがわ力る。  [0051] The following can be understood from Table 1.
[0052] 実施例 1で得られた塩ィ匕ビュル系繊維は、すべての特性に関して良ぐ目標とする 塩ィ匕ビニル系繊維が得られた。  [0052] The chloride-type fiber obtained in Example 1 gave a vinyl chloride-type target fiber, which is good for all properties.
[0053] 実施例 2で得られた塩ィ匕ビュル系繊維は、実施例 1の配合中のポリオールを配合し な力つたものである力 変色性においてわずかに難はある力 全ての特性値に関してThe salted fibers obtained in Example 2 are those obtained by blending the polyol in the composition of Example 1 and having a slight difficulty in the color changeability. With respect to all the characteristic values
、製品として問題のない範囲内のものであった。 , It was in the range without problems as a product.
[0054] 実施例 3で得られた塩化ビニル系繊維は、実施例 1で得られた塩化ビニル系繊維 に比べて糸切れ頻度に多少難はあるが、全ての特性値に関して、製品として問題の な 、範囲内のものであつた。 The vinyl chloride-based fiber obtained in Example 3 has some difficulty in the thread breakage frequency compared to the vinyl chloride-based fiber obtained in Example 1, but all the characteristic values have problems as a product. It was in the range.
[0055] 比較例 1で得られた塩ィ匕ビュル系繊維は、ハイド口タルサイト系熱安定剤の配合量 が少な力つたために、糸切れ頻度が多くなつて紡糸が困難となり、ロングラン性が悪 かった。 [0055] The salted boule fiber obtained in Comparative Example 1 has a high content of yarn breakage frequency and is difficult to be spun because the compounding amount of the hydride-talcite-based heat stabilizer is small, so that the long run property is obtained. Was bad.
[0056] 比較例 2で得られた塩ィ匕ビュル系繊維は、ハイド口タルサイト系熱安定剤の配合量 が多すぎるために、初期着色性が悪力つた。 [0057] 比較例 3で得られた塩ィ匕ビュル系繊維は、エポキシィ匕合物の配合量が少な力つた ために、ロングラン性と変色性とが悪力つた。 [0056] The salted boule based fibers obtained in Comparative Example 2 had poor initial colorability because the blending amount of the hydrotalcite-based heat stabilizer was too large. [0057] The chloride-based fiber obtained in Comparative Example 3 had a long-running property and a discoloring property because the blending amount of the epoxy compound was small.
[0058] 比較例 4で得られた塩ィ匕ビュル系繊維は、エポキシィ匕合物の配合量が多すぎたた めに、糸切れ頻度が多くなつて紡糸が困難となり、ロングラン性が悪力つた。 [0058] The chloride-based fiber obtained in Comparative Example 4 has a high yarn breakage frequency due to too much compounding amount of the epoxy compound, which makes spinning difficult, and the long-run property is bad. It was
産業上の利用可能性  Industrial applicability
[0059] 本発明の塩化ビュル系繊維は、例えば、ウイッグ、ヘアピース、ブレード、ェクステン シヨンヘアー等の頭髪装飾製品の製造において用いられる人毛に似た艷、色相、及 び、風合 、を有する塩ィ匕ビュル系繊維とすることができる。 [0059] The chloride-based boule fiber of the present invention has a salt, for example, having wrinkles, hues, and a texture similar to human hair used in the production of hair decoration products such as wigs, hairpieces, blades, and fixture hairs. It can be an ibule based fiber.

Claims

請求の範囲 The scope of the claims
[1] (a)塩ィ匕ビ二ル系榭脂 100質量部、(b)ハイド口タルサイト系熱安定剤 0. 2-5. 0 質量部、及び、(c)エポキシィ匕合物 0. 2— 10. 0質量部を含有する塩化ビニル系榭 脂組成物で構成されていることを特徴とする塩ィ匕ビニル系繊維。  [1] (a) 100 parts by mass of vinyl chloride-based resin, (b) thermal stabilizer based on hyde-portal oxide 0.2-5 parts by mass, and (c) epoxy compound 0 2— A vinyl chloride-based fiber comprising a vinyl chloride-based resin composition containing 10.0 parts by mass.
[2] 前記エポキシ化合物が、エポキシ化大豆油、エポキシ化亜麻仁油、エポキシ化桐 油、エポキシ化魚油、エポキシィ匕牛脂油、エポキシィ匕ひまし油、エポキシィ匕サフラヮ 一油等のエポキシ化動植物油、エポキシ含有メタクリル酸ィ匕合物、エポキシ化ステア リン酸メチノレ、エポキシィ匕ポリブタジエン、トリス(エポキシプロピル)イソシァヌレート、 エポキシ化トール油脂肪酸エステル、エポキシィ匕亜麻仁油脂肪酸エステル、ビュル クロへキセンジェポキサイド、ジシクロへキセンカルボキシレート、ビスフエノール Aジ グリシジルエーテル、グリセリンポリグリシジルエーテル、及び、シクロへキサンジメタノ 一ルポリグリシジルエーテル力も選ばれる少なくとも一種のエポキシィ匕合物であること を特徴とする請求項 1に記載の塩化ビニル系繊維。  [2] The epoxy compound is epoxidized animal oil such as epoxidized soybean oil, epoxidized linseed oil, epoxidized tung oil, epoxidized fish oil, epoxidized calf oil, epoxidized linseed oil, epoxidized safflower oil, etc. Methacrylic acid compound, epoxidized stearic acid phosphoric acid methynole, epoxy dipolybutadiene, tris (epoxypropyl) isocyanurate, epoxidized tall oil fatty acid ester, epoxy dihydric linseed oil fatty acid ester, buhl chlorhexene poxide, dicyclohexylene Carboxylate, bis-phenol A diglycidyl ether, glycerine polyglycidyl ether, and at least one epoxy compound selected from cyclohexanedimethanoyl polyglycidyl ether. Vinyl chloride fiber mounting.
[3] 前記塩ィ匕ビュル系榭脂組成物が、さらに、(d)窒素含有ポリオール 0. 01-2. 0質 量部を含有することを特徴とする請求項 1又は 2に記載の塩化ビニル系繊維。  [3] The chloride according to any one of claims 1 and 2, wherein the salt-like grease composition further comprises (d) a nitrogen-containing polyol in an amount of 0.1-20.0 parts by mass. Vinyl fiber.
[4] 前記窒素含有ポリオール力 トリス(2—ヒドロキシェチル)イソシァヌレート、トリス(3— ヒドロキシプロピル)イソシァヌレート、又は、トリス(4ーヒドロキシブチノレ)イソシァヌレー トであることを特徴とする請求項 3に記載の塩ィ匕ビニル系繊維。  [4] The nitrogen-containing polyol according to claim 3, which is tris (2-hydroxyethyl) isocyanurate, tris (3-hydroxypropyl) isocyanurate, or tris (4-hydroxybutynore) isocyanurate. Salt and vinyl fibers described.
[5] (a)塩ィ匕ビ二ル系榭脂 100質量部、(b)ハイド口タルサイト系熱安定剤 0. 2-5. 0 質量部、及び、(c)エポキシィ匕合物 0. 2— 10. 0質量部を含有する塩化ビニル系榭 脂組成物を 170— 190°Cの温度で溶融紡糸することを特徴とする塩ィ匕ビニル系繊維 の製造方法。  [5] (a) 100 parts by mass of vinyl chloride-based resin, (b) thermal stability agent for hydite mouth talcite 0.2-5. 0 parts by mass, and (c) epoxy compound 0 A method for producing a vinyl chloride-based fiber comprising melt spinning a vinyl chloride resin composition containing 1 to 10 parts by mass at a temperature of 170 to 190 ° C.
[6] 前記溶融紡糸した塩化ビニル系繊維を 90— 120°Cの温度に保持した空気雰囲気 下で 2— 4倍まで延伸した後、この延伸した塩ィ匕ビュル系繊維を 110— 140°Cの温度 に保持した空気雰囲気下で処理前の 60— 100%の長さになるまで熱弛緩させること を特徴とする請求項 5に記載の塩化ビニル系繊維の製造方法。  [6] The melt-spun vinyl chloride fiber is drawn to 2 to 4 times in an air atmosphere maintained at a temperature of 90 to 120 ° C., and then this drawn chloride-based fiber is taken to 110 to 140 ° C. The method for producing a vinyl chloride-based fiber according to claim 5, characterized in that heat relaxation is performed to a length of 60 to 100% before treatment under an air atmosphere maintained at a temperature of
[7] 前記塩ィ匕ビュル系榭脂組成物が、さらに、(d)窒素含有ポリオール 0. 01-2. 0質 量部を含有することを特徴とする請求項 5又は 6に記載の塩ィ匕ビュル系繊維の製造 [7] The salt according to claim 5 or 6, characterized in that the salt-and-bole based fat composition further comprises (d) a nitrogen-containing polyol in an amount of 0.1-20.0 parts by mass. Manufacture of textiles
o請 Zdf/ェ:) d 91 C8CCC0/S00Z OAV o Z Zdf /: :) d 91 C8 CCC 0 / S00 Z OAV
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101300377B (en) * 2005-11-02 2011-05-18 电气化学工业株式会社 Fiber with modified cross section and fiber for artificial hair formed of the same
KR101044900B1 (en) * 2006-02-28 2011-06-28 덴끼 가가꾸 고교 가부시키가이샤 Vinyl chloride resin fiber and method for producing same
CN103073830A (en) * 2013-02-16 2013-05-01 哈尔滨中大型材科技股份有限公司 Preparation method of maleic anhydride grafted chlorinated polyvinyl chloride composite material

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20120111990A (en) * 2011-03-31 2012-10-11 유인식 The manufacturing method of the synthetic textiles included plant fatty acid
CN108395643B (en) * 2018-03-23 2020-02-07 邵阳学院 Modified hydrocalumite for PVC heat stabilizer and clean preparation method thereof

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11100714A (en) * 1997-07-31 1999-04-13 Kanegafuchi Chem Ind Co Ltd Vinyl chloride-based fiber and its production
JP2000328355A (en) * 1999-05-20 2000-11-28 Kanegafuchi Chem Ind Co Ltd Vinyl chloride-based fiber and its production
JP2001279523A (en) * 2000-03-29 2001-10-10 Toyo Chem Co Ltd Vinyl chloride-based resin composition for fiber and stabilizer composition for vinyl chloride-based resin for fiber

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5836012B2 (en) * 1980-11-07 1983-08-06 アデカ・ア−ガス化学株式会社 Halogen-containing resin composition
CN1089820C (en) * 1997-03-11 2002-08-28 钟渊化学工业株式会社 Vinyl chloride fibers and process for preparing the same
JP2000328358A (en) * 1999-05-11 2000-11-28 Toray Ind Inc Soft polyester fiber and fabric
WO2004090208A1 (en) * 2003-04-04 2004-10-21 Denki Kagaku Kogyo Kabushiki Kaisha Polyvinyl chloride fiber, process for producing the same, and use thereof
JP4828428B2 (en) * 2004-09-29 2011-11-30 株式会社カネカ Polyvinyl chloride fiber with little initial coloration
WO2006035863A1 (en) * 2004-09-30 2006-04-06 Kaneka Corporation Polyvinyl chloride fiber and process for production thereof

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11100714A (en) * 1997-07-31 1999-04-13 Kanegafuchi Chem Ind Co Ltd Vinyl chloride-based fiber and its production
JP2000328355A (en) * 1999-05-20 2000-11-28 Kanegafuchi Chem Ind Co Ltd Vinyl chloride-based fiber and its production
JP2001279523A (en) * 2000-03-29 2001-10-10 Toyo Chem Co Ltd Vinyl chloride-based resin composition for fiber and stabilizer composition for vinyl chloride-based resin for fiber

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101300377B (en) * 2005-11-02 2011-05-18 电气化学工业株式会社 Fiber with modified cross section and fiber for artificial hair formed of the same
KR101044900B1 (en) * 2006-02-28 2011-06-28 덴끼 가가꾸 고교 가부시키가이샤 Vinyl chloride resin fiber and method for producing same
CN103073830A (en) * 2013-02-16 2013-05-01 哈尔滨中大型材科技股份有限公司 Preparation method of maleic anhydride grafted chlorinated polyvinyl chloride composite material
CN103073830B (en) * 2013-02-16 2015-04-29 哈尔滨中大型材科技股份有限公司 Preparation method of maleic anhydride grafted chlorinated polyvinyl chloride composite material

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