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CN105350299A - Automatic temperature adjustment breathable type outdoor sportswear fabric and preparation method - Google Patents

Automatic temperature adjustment breathable type outdoor sportswear fabric and preparation method Download PDF

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Publication number
CN105350299A
CN105350299A CN201510635502.6A CN201510635502A CN105350299A CN 105350299 A CN105350299 A CN 105350299A CN 201510635502 A CN201510635502 A CN 201510635502A CN 105350299 A CN105350299 A CN 105350299A
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fiber
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prepared
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CN105350299B (en
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董好杰
倪宏竹
张倩
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Henan University of Science and Technology
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Henan University of Science and Technology
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    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10Treating 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
    • D06M13/144Alcohols; Metal alcoholates
    • AHUMAN NECESSITIES
    • A41WEARING APPAREL
    • A41DOUTERWEAR; PROTECTIVE GARMENTS; ACCESSORIES
    • A41D31/00Materials specially adapted for outerwear
    • AHUMAN NECESSITIES
    • A41WEARING APPAREL
    • A41DOUTERWEAR; PROTECTIVE GARMENTS; ACCESSORIES
    • A41D31/00Materials specially adapted for outerwear
    • A41D31/04Materials specially adapted for outerwear characterised by special function or use
    • A41D31/14Air permeable, i.e. capable of being penetrated by gases
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01DMECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D1/00Treatment of filament-forming or like material
    • D01D1/02Preparation of spinning solutions
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01DMECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D5/00Formation of filaments, threads, or the like
    • D01D5/0007Electro-spinning
    • D01D5/0015Electro-spinning characterised by the initial state of the material
    • D01D5/003Electro-spinning characterised by the initial state of the material the material being a polymer solution or dispersion
    • 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
    • D01F2/00Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof
    • D01F2/06Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from viscose
    • D01F2/08Composition of the spinning solution or the bath
    • 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
    • D01F8/00Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
    • D01F8/04Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
    • D01F8/12Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers with at least one polyamide as constituent
    • 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
    • D01F8/00Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
    • D01F8/04Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
    • D01F8/16Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers with at least one other macromolecular compound obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds as constituent
    • DTEXTILES; PAPER
    • D02YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
    • D02GCRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
    • D02G3/00Yarns or threads, e.g. fancy yarns; Processes or apparatus for the production thereof, not otherwise provided for
    • D02G3/02Yarns or threads characterised by the material or by the materials from which they are made
    • D02G3/04Blended or other yarns or threads containing components made from different materials
    • D02G3/045Blended or other yarns or threads containing components made from different materials all components being made from artificial or synthetic material
    • DTEXTILES; PAPER
    • D03WEAVING
    • D03DWOVEN FABRICS; METHODS OF WEAVING; LOOMS
    • D03D15/00Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M10/00Physical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. ultrasonic, corona discharge, irradiation, electric currents, or magnetic fields; Physical treatment combined with treatment with chemical compounds or elements
    • D06M10/04Physical treatment combined with treatment with chemical compounds or elements
    • D06M10/08Organic compounds
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    • D06M10/00Physical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. ultrasonic, corona discharge, irradiation, electric currents, or magnetic fields; Physical treatment combined with treatment with chemical compounds or elements
    • D06M10/04Physical treatment combined with treatment with chemical compounds or elements
    • D06M10/08Organic compounds
    • D06M10/10Macromolecular compounds
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    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10Treating 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
    • D06M13/144Alcohols; Metal alcoholates
    • D06M13/148Polyalcohols, e.g. glycerol or glucose
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    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/01Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural macromolecular compounds or derivatives thereof
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    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/01Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural macromolecular compounds or derivatives thereof
    • D06M15/03Polysaccharides or derivatives thereof
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    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/53Polyethers
    • AHUMAN NECESSITIES
    • A41WEARING APPAREL
    • A41DOUTERWEAR; PROTECTIVE GARMENTS; ACCESSORIES
    • A41D2400/00Functions or special features of garments
    • A41D2400/10Heat retention or warming
    • AHUMAN NECESSITIES
    • A41WEARING APPAREL
    • A41DOUTERWEAR; PROTECTIVE GARMENTS; ACCESSORIES
    • A41D2400/00Functions or special features of garments
    • A41D2400/36Deoderising or perfuming
    • AHUMAN NECESSITIES
    • A41WEARING APPAREL
    • A41DOUTERWEAR; PROTECTIVE GARMENTS; ACCESSORIES
    • A41D2500/00Materials for garments
    • A41D2500/20Woven
    • AHUMAN NECESSITIES
    • A41WEARING APPAREL
    • A41DOUTERWEAR; PROTECTIVE GARMENTS; ACCESSORIES
    • A41D31/00Materials specially adapted for outerwear
    • A41D31/04Materials specially adapted for outerwear characterised by special function or use
    • A41D31/30Antimicrobial, e.g. antibacterial
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    • D06M2101/00Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
    • D06M2101/02Natural fibres, other than mineral fibres
    • D06M2101/04Vegetal fibres
    • D06M2101/06Vegetal fibres cellulosic
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    • D06M2101/00Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
    • D06M2101/16Synthetic fibres, other than mineral fibres
    • D06M2101/18Synthetic fibres consisting of macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M2101/26Polymers or copolymers of unsaturated carboxylic acids or derivatives thereof
    • D06M2101/28Acrylonitrile; Methacrylonitrile
    • DTEXTILES; PAPER
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    • D06M2101/16Synthetic fibres, other than mineral fibres
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    • D06M2101/16Synthetic fibres, other than mineral fibres
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    • D06M2101/34Polyamides
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    • D10INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
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    • D10B2201/00Cellulose-based fibres, e.g. vegetable fibres
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    • D10B2201/22Cellulose-derived artificial fibres made from cellulose solutions
    • D10B2201/24Viscose
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    • D10B2211/20Protein-derived artificial fibres
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    • D10B2321/00Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D10B2321/10Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds polymers of unsaturated nitriles, e.g. polyacrylonitrile, polyvinylidene cyanide
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    • D10B2331/00Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products
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Abstract

一种自动调温透气型户外运动衣面料及其制备方法,由经纱和纬纱交织成预制体,将预制体浸渍后,制得面料;其中,经纱由改性锦纶纤维20-30份、改性粘胶纤维45-50份和改性聚丙烯腈纤维20-35份组成;纬纱由改性涤纶纤维50-60份和牛奶纤维40-50份组成。本发明将制得的经纱和纬纱合成预制体,并将预制体置于悬浮乳液中,在超声波下浸渍10-14h后,取出烘干,制得运动衣面料。制备的运动衣面料具有自动调温性、高透气性和吸汗性,使运动过程中更加舒适、安全、健康。An automatic temperature-regulating breathable outdoor sportswear fabric and a preparation method thereof. Warp yarns and weft yarns are interwoven into preforms, and the preforms are impregnated to obtain fabrics; wherein, the warp yarns are made of 20-30 parts of modified nylon fibers, modified It consists of 45-50 parts of viscose fiber and 20-35 parts of modified polyacrylonitrile fiber; the weft yarn consists of 50-60 parts of modified polyester fiber and 40-50 parts of milk fiber. The invention synthesizes the prepared warp yarn and weft yarn into a preform, places the preform in a suspending emulsion, immerses the preform under ultrasonic waves for 10-14 hours, takes it out and dries, and obtains the sportswear fabric. The prepared sportswear fabric has automatic temperature regulation, high air permeability and sweat absorption, which makes it more comfortable, safe and healthy during exercise.

Description

一种自动调温透气型户外运动衣面料及其制备方法A kind of automatic temperature-regulating breathable outdoor sportswear fabric and its preparation method

技术领域 technical field

本发明涉及运动衣领域,具体涉及一种自动调温透气型户外运动衣面料及其制备方法。 The invention relates to the field of sportswear, in particular to an automatic temperature-regulating breathable outdoor sportswear fabric and a preparation method thereof.

背景技术 Background technique

衣、食、住、行作为人民生活的基本需求,随着科技的进步,人民的生活水平在逐步提高,人民的需求也在不断提高。当前,户外体育运动已经成为人们工作之余的一项重要运动项目。由于在运动的过程中,人体会产生热量和汗液,而普通的运动服装不透气、不吸汗,这样运动过程中人们会感到非常不舒适,降低运动的乐趣,因此需要研究出一款高透气性、智能调温的运动纺织品为人们提供一种冷时放热,热时吸热,消除运动过程中温度变化而产生的冷热感,提高人们运动的乐趣。 Clothing, food, housing, and transportation are the basic needs of people's lives. With the advancement of science and technology, people's living standards are gradually improving, and people's needs are also constantly improving. At present, outdoor sports have become an important sport for people after work. Since the human body produces heat and sweat during exercise, and ordinary sportswear is airtight and does not absorb sweat, people will feel very uncomfortable during exercise and reduce the enjoyment of exercise. Therefore, it is necessary to develop a high-breathability 1. Intelligent temperature-adjusting sports textiles provide people with a kind of heat release when cold and heat absorption when hot, eliminating the feeling of cold and heat caused by temperature changes during exercise, and improving people's enjoyment of exercise.

现在,体育事业蓬勃发展,调温纺织品已经成为国内外纺织功能性产品的研究热点。在国内,调温纤维的研究和应用还处于起步阶段,市场还没有完全成熟的产品。但由于调温纤维具有储热调温功能,并且具有优良的可与其他各种纤维的混纺性,其应用范围及其广阔,因此,必将具有广阔的市场发展空间。 Now, with the vigorous development of the sports industry, temperature-regulating textiles have become a research hotspot of textile functional products at home and abroad. In China, the research and application of temperature-regulating fibers are still in their infancy, and there are no fully mature products in the market. However, because the temperature-regulating fiber has heat storage and temperature-regulating functions, and has excellent blending properties with other various fibers, its application range is extremely wide, so it will definitely have a broad market development space.

发明内容 Contents of the invention

本发明的目的在于克服现有技术的不足,提供一种自动调温透气型户外运动衣面料及其制备方法。 The purpose of the present invention is to overcome the deficiencies of the prior art, and provide an automatic temperature-regulating breathable outdoor sportswear fabric and a preparation method thereof.

本发明为了解决上述问题所采取的技术方案为:一种自动调温透气型户外运动衣面料,由经纱和纬纱交织成预制体,将预制体浸渍后,制得面料;其中,经纱由以下重量组份的原料组成:改性锦纶纤维20-30份、改性粘胶纤维45-50份和改性聚丙烯腈纤维20-35份;纬纱由以下重量组份的原料组成:改性涤纶纤维50-60份和牛奶纤维40-50份。 The technical solution adopted by the present invention in order to solve the above problems is: an automatic temperature-regulating breathable outdoor sportswear fabric, which is interwoven with warp yarns and weft yarns into a prefabricated body, and the prefabricated body is impregnated to obtain a fabric; wherein the warp yarn is made of the following weight: Raw material composition of components: 20-30 parts of modified nylon fiber, 45-50 parts of modified viscose fiber and 20-35 parts of modified polyacrylonitrile fiber; the weft yarn is composed of raw materials with the following weight components: modified polyester fiber 50-60 servings and 40-50 servings of milk fiber.

本发明中,所述的改性锦纶纤维为聚乙二醇接枝聚酰胺6,其中,聚乙二醇分子量为4000-6000。 In the present invention, the modified nylon fiber is polyethylene glycol grafted polyamide 6, wherein the molecular weight of polyethylene glycol is 4000-6000.

本发明中,所述的改性粘胶纤维由以下重量组份的原料组成:粘胶纺丝液90-95份,微胶囊复配相变材料5-10份。 In the present invention, the modified viscose fiber is composed of the following raw materials by weight: 90-95 parts of viscose spinning solution, and 5-10 parts of microcapsule compound phase change material.

本发明中的改性涤纶纤维为聚乙二醇接枝聚对苯二甲酸乙二醇酯,其中,聚乙二醇分子量为1000-2000。 The modified polyester fiber in the present invention is polyethylene glycol grafted polyethylene terephthalate, wherein the molecular weight of polyethylene glycol is 1000-2000.

一种自动调温透气型户外运动衣面料的制备方法,包括以下步骤: A method for preparing an automatic temperature-regulating breathable outdoor sportswear fabric, comprising the following steps:

步骤一、将重量比为2:4:1的正十四烷、正十六烷、正二十烷配置成混合溶液,将混合溶液置于三口瓶中水浴加热,水浴温度为70-80℃,以1000-1300rpm的转速搅拌10-15min后,按照混合溶液:乳化剂:PVA水溶液=10:0.2:0.5-1.0的重量比,加入乳化剂和PVA水溶液,以450-600rpm的转速搅拌1-1.5h,形成乳液,然后加入浓度为10%的稀硫酸,调节乳液pH至4-5,备用; Step 1. Prepare n-tetradecane, n-hexadecane, and n-eicosane with a weight ratio of 2:4:1 to form a mixed solution, place the mixed solution in a three-necked bottle and heat it in a water bath, and the temperature of the water bath is 70-80°C , after stirring at a speed of 1000-1300rpm for 10-15min, according to the weight ratio of mixed solution: emulsifier: PVA aqueous solution = 10:0.2:0.5-1.0, add emulsifier and PVA aqueous solution, and stir at a speed of 450-600rpm for 1- 1.5h to form an emulsion, then add dilute sulfuric acid with a concentration of 10%, adjust the pH of the emulsion to 4-5, and set aside;

步骤二、将摩尔比为1:4.5-5的三聚氰胺和甲醛置于容器中形成溶液,于75-80℃密闭搅拌0.5h,然后加入浓度为10-15%的Na2CO3稀溶液,调节溶液的pH至9-10,45-50℃搅拌至溶液澄清透明;然后照该溶液:乳液=3:5的体积比,将该溶液加入步骤一制备的乳液中,搅拌2.5-3h,形成悬浮液,用离心机将悬浮液进行分离,离心速度为2500-3000rpm,将离心得到的沉淀分别用乙二醇和去离子水洗涤3-5次,然后置于40-50℃烘箱中烘干10-12h,制得微胶囊复配相变材料,备用; Step 2: Put melamine and formaldehyde with a molar ratio of 1:4.5-5 in a container to form a solution, and stir in a sealed container at 75-80°C for 0.5h, then add a diluted solution of Na 2 CO 3 with a concentration of 10-15%, and adjust The pH of the solution is 9-10, and stirred at 45-50°C until the solution is clear and transparent; then according to the volume ratio of the solution:emulsion=3:5, add the solution to the emulsion prepared in step 1, stir for 2.5-3h, and form a suspension Separate the suspension with a centrifuge at a speed of 2500-3000rpm, wash the precipitate obtained by centrifugation with ethylene glycol and deionized water for 3-5 times, and then dry it in an oven at 40-50°C for 10- 12h, the microcapsule composite phase change material was prepared and set aside;

步骤三、按照粘胶纺丝液90-95份、微胶囊复配相变材料5-10份的重量份数,称取粘胶纺丝液和步骤二制得的微胶囊复配相变材料,混合后经喷丝板挤出,制得改性粘胶纤维,备用; Step 3, according to the parts by weight of 90-95 parts of viscose spinning solution and 5-10 parts of microcapsule compound phase change material, weigh the viscose spinning solution and the microcapsule compound phase change material prepared in step 2 , mixed and extruded through a spinneret to obtain a modified viscose fiber for subsequent use;

步骤四、按照紫外光固化丙烯酸酯粘合剂70-80份、微胶囊复配相变材料5-7份的重量份数,称取紫外光固化丙烯酸酯粘合剂和步骤二制得的微胶囊复配相变材料,混合得复合粘合剂,将复合粘合剂涂覆在聚丙烯腈纤维上,经紫外光照射,得到改性聚丙烯腈纤维,备用; Step 4, according to the parts by weight of 70-80 parts of UV-curable acrylate adhesive and 5-7 parts of microcapsule composite phase-change material, weigh the UV-curable acrylate adhesive and the microcapsule prepared in step 2. Capsules are compounded with phase change materials, mixed to obtain a composite adhesive, coated on the polyacrylonitrile fiber by the composite adhesive, and irradiated with ultraviolet light to obtain a modified polyacrylonitrile fiber, which is ready for use;

步骤五、将涤纶纤维放入等离子体处理仪中,抽真空用氧气处理0.5-1.5h,然后将处理过的涤纶纤维直接浸渍在质量分数为20-35%聚乙二醇的溶液中,在25-30℃的温度下浸泡6-7h,取出晾干,然后用Ar等离子处理,处理时间为1-2.5min,功率为100-200W,压强为50-60Pa,处理后,用蒸馏水超声清洗6-8min,晾干后,制得改性涤纶纤维,备用; Step 5. Put the polyester fiber into the plasma treatment apparatus, vacuumize and treat it with oxygen for 0.5-1.5h, and then directly immerse the treated polyester fiber in a solution with a mass fraction of 20-35% polyethylene glycol. Soak at a temperature of 25-30°C for 6-7h, take it out and dry it, and then treat it with Ar plasma, the treatment time is 1-2.5min, the power is 100-200W, and the pressure is 50-60Pa. After treatment, it is ultrasonically cleaned with distilled water for 6 -8min, after drying, the modified polyester fiber is obtained, which is for subsequent use;

步骤六、将聚酰胺6和聚乙二醇按照50-90:10-50的质量比置于质量分数为98%的甲酸中,在30-40℃的温度下搅拌1.5-2h,形成质量分数为14-17%的均匀纺丝液,通过静电纺丝机进行纺丝,纺丝液流速为0.2-0.4ml/h,喷嘴口径为1-1.2mm,得到改性锦纶纤维,备用; Step six, polyamide 6 and polyethylene glycol are placed in formic acid with a mass fraction of 98% according to the mass ratio of 50-90:10-50, and stirred at a temperature of 30-40°C for 1.5-2h to form a mass fraction It is 14-17% uniform spinning solution, which is spun by an electrospinning machine. The flow rate of the spinning solution is 0.2-0.4ml/h, and the nozzle diameter is 1-1.2mm, so as to obtain modified nylon fiber and set aside;

步骤七、按照所述改性锦纶纤维20-30份、改性粘胶纤维45-50份和改性聚丙烯腈纤维20-35份的重量份数,将步骤六制得的改性锦纶纤维、步骤三制得的改性粘胶纤维、步骤四制得的改性聚丙烯腈纤维合成轻纱;按照改性涤纶纤维50-60份和牛奶纤维40-50份的重量份数,将牛奶纤维和步骤五制得的改性涤纶纤维合成纬纱;最后将经纱和纬纱合成预制体,备用; Step 7, according to the parts by weight of 20-30 parts of modified nylon fiber, 45-50 parts of modified viscose fiber and 20-35 parts of modified polyacrylonitrile fiber, the modified nylon fiber obtained in step 6 , the modified viscose fiber that step 3 makes, the modified polyacrylonitrile fiber synthetic light yarn that step 4 makes; According to the parts by weight of 50-60 parts of modified polyester fiber and 40-50 parts of milk fiber, milk The fiber and the modified polyester fiber prepared in step 5 synthesize the weft yarn; finally, the warp yarn and the weft yarn are synthesized into a prefabricated body for subsequent use;

步骤八、按照下列重量组份,称取各材料进行混合:壳聚糖2-5份、丙三醇2-3份、乙醇60-75份、植物蜡2-2.5份、负离子粉1-5份,制得悬浮乳液,将步骤七制得的预制体置于该悬浮乳液中,在超声波下浸渍10-14h后,取出烘干,制得运动衣面料。 Step 8, according to the following weight components, weigh each material and mix: 2-5 parts of chitosan, 2-3 parts of glycerol, 60-75 parts of ethanol, 2-2.5 parts of vegetable wax, 1-5 parts of negative ion powder part to prepare a suspoemulsion, place the prefabricated body prepared in step 7 in the suspoemulsion, immerse it under ultrasonic waves for 10-14 hours, take it out and dry it, and obtain a sportswear fabric.

聚酰胺6具有强度高、回弹性好、耐疲劳、可染性和耐腐蚀、耐虫蛀等优良性能,密度低于大多数纤维品种,耐磨性能则优于合成纤维其他品种,适用于户外运动服饰中;聚乙二醇在常温下可由无定形到结晶的转变获得一定的相变焓,并以潜热的形式吸收、储存、释放,可作为相变调温、储能材料。 Polyamide 6 has excellent properties such as high strength, good resilience, fatigue resistance, dyeability, corrosion resistance, and insect resistance. Its density is lower than most fiber varieties, and its wear resistance is better than other synthetic fibers. It is suitable for outdoor use In sportswear; polyethylene glycol can obtain a certain phase change enthalpy from amorphous to crystallization at room temperature, and absorb, store, and release it in the form of latent heat, and can be used as a phase change temperature adjustment and energy storage material.

本发明中以聚乙二醇为相变材料,以聚酰胺6(PA6)为高分子载体,通过共混静电纺丝方法,将调温材料聚乙二醇引入至高分子载体PA6中,制备相变纳米调温纤维。实验中发现,聚乙二醇与PA6共混纺丝纺出的纤维并未出现分离相,二者相容性良好,并且PA6大分子与聚乙二醇存在氢键结合,随着聚乙二醇的混入,纺丝液的黏度改善,在一定程度上有利于获得形貌规整、分布均匀的纤维,且纳米纤维的直径有一定程度的提高,当PA6与聚乙二醇的共混比例为一定时,可获得形貌变得规整、无珠状物、纤维之间无黏连的PA6/聚乙二醇共混纳米纤维,纤维的平均直径为(100±12)nm;随着聚乙二醇共混比例的提高,相变纳米纤维的熔融温度和熔融焓值逐渐增大,这是由于随着聚乙二醇在相变纳米纤维中含量的增加,其固态-液态相变储存的能量也逐渐增大,且不同共混比例的相变纳米纤维的熔融温度和焓值均小于聚乙二醇,这是由于高分子材料PA6的熔融温度较高,其在聚乙二醇相变调温范围内保持固态形状不发生改变且不提供热焓值;其次,PA6与聚乙二醇之间形成氢键结合以及相变纳米纤维的三维纤维网状结构,也对相变材料聚乙二醇的相转变有抑制作用,导致相变纤维的熔融温度和焓值均小于相变材料。 In the present invention, polyethylene glycol is used as the phase change material, polyamide 6 (PA6) is used as the polymer carrier, and the temperature-regulating material polyethylene glycol is introduced into the polymer carrier PA6 through a blending electrospinning method to prepare the phase change material. Change nano temperature regulating fiber. In the experiment, it was found that the fibers spun out of the blended spinning of polyethylene glycol and PA6 did not appear separated phases, and the compatibility between the two was good, and there was a hydrogen bond between the PA6 macromolecule and polyethylene glycol, and with the polyethylene glycol The viscosity of the spinning solution is improved to a certain extent, which is beneficial to obtain fibers with regular shape and uniform distribution, and the diameter of nanofibers is increased to a certain extent. When the blending ratio of PA6 and polyethylene glycol is 1 Timing, PA6/polyethylene glycol blended nanofibers with regular morphology, no beads, and no adhesion between fibers can be obtained. The average diameter of the fibers is (100±12) nm; With the increase of alcohol blending ratio, the melting temperature and melting enthalpy of phase change nanofibers gradually increase, which is due to the energy stored in its solid-liquid phase transition with the increase of polyethylene glycol content in phase change nanofibers. It also increases gradually, and the melting temperature and enthalpy of phase change nanofibers with different blending ratios are lower than that of polyethylene glycol, which is due to the higher melting temperature of polymer material PA6, and its The shape of the solid state does not change in the temperature range and does not provide enthalpy; secondly, the formation of hydrogen bonding between PA6 and polyethylene glycol and the three-dimensional fiber network structure of phase-change nanofibers also affect the phase-change material polyethylene glycol. Alcohol has an inhibitory effect on the phase transition, resulting in the melting temperature and enthalpy of the phase change fiber being lower than that of the phase change material.

粘胶纤维具有较高的强力和耐疲劳性能,并且具有吸湿性,可以吸收运动过程中产生汗液;将微胶囊复配相变材料加入粘胶纺丝液中,经喷丝板挤出后,制得含有微胶囊复配相变材料的改性粘胶纤维既具有较高的强力、耐疲劳性能和吸湿性,同时也具有自调温性能,价格成本低,并且环保。 Viscose fiber has high strength and fatigue resistance, and has hygroscopicity, which can absorb sweat produced during exercise; add microcapsule compound phase change materials into viscose spinning solution, and extrude through the spinneret, The prepared modified viscose fiber containing the microcapsule compound phase change material not only has high strength, fatigue resistance and hygroscopicity, but also has self-regulating temperature performance, low price and cost, and is environmentally friendly.

聚丙烯腈纤维具有柔软、膨松、易染、色泽鲜艳、耐光、抗菌,弹性较好、透气性好的特点,运用紫外光固化丙烯酸酯粘合剂将微胶囊复配相变材料粘接在聚丙烯腈纤维上,使聚丙烯腈纤维在具有自身优良性能的基础上同时兼具自调温功能。采用的紫外光固化丙烯酸酯粘合剂,固化光源为紫外光时的光固化粘合剂,主体成分是丙烯酸酯类,可通过改变其分子链结构和相对分子质量的大小,改变粘合剂的硬度、柔顺性、粘附性、耐介质性、耐久性和固化速度,并且固化后强度较好,透明度高:固化温度低,室温下即可固化。 Polyacrylonitrile fiber has the characteristics of softness, bulkiness, easy dyeing, bright color, light resistance, antibacterial, good elasticity and good air permeability. The microcapsule compound phase change material is bonded to the On the polyacrylonitrile fiber, the polyacrylonitrile fiber has the function of self-temperature adjustment on the basis of its own excellent performance. The UV-curable acrylate adhesive used is a photo-curable adhesive when the curing light source is ultraviolet light. The main component is acrylate, which can change the molecular chain structure and relative molecular weight of the adhesive. Hardness, flexibility, adhesion, medium resistance, durability and curing speed, and good strength after curing, high transparency: low curing temperature, can be cured at room temperature.

涤纶纤维对伸长、压缩、弯曲等形变的恢复能力与羊毛接近,具有强度高、弹性好、耐磨性好、耐光性好、耐腐蚀,利用低温等离子体处理涤纶纤维将聚乙二醇截止到涤纶纤维上,能使纤维表面产生活性自由基,形成亲水中,提高纤维的吸湿性能,将其做运动衣材料,可以吸收运动过程产生的汗液。 The recovery ability of polyester fiber to elongation, compression, bending and other deformations is close to that of wool. When applied to polyester fiber, active free radicals can be generated on the surface of the fiber, forming hydrophilic, improving the moisture absorption performance of the fiber, making it a sportswear material, which can absorb sweat generated during exercise.

牛奶纤维具有较好的耐磨性、抗起球性、着色性、柔软性、亲肤性、透气性、导湿性,并且对皮肤有养护作用;由于其不使用甲醛偶氮类助剂或原料,纤维甲醛含量为零;富含对人体有益的十八种氨基酸,能促进人体细胞新陈代谢,防止皮肤衰老、瘙痒,营养肌肤;具有天然保湿因子,因此能保持皮肤水份含量,使皮肤柔润光滑,减少皱纹,具有广谱抑菌功能,持久性强,天然抑菌功能达99%以上,抗菌率达80%以上。 Milk fiber has good abrasion resistance, anti-pilling, coloring, softness, skin-friendly, air permeability, moisture permeability, and has a maintenance effect on the skin; because it does not use formaldehyde azo additives or raw materials , fiber formaldehyde content is zero; rich in 18 kinds of amino acids that are beneficial to the human body, can promote the metabolism of human cells, prevent skin aging, itching, and nourish the skin; it has natural moisturizing factors, so it can maintain the moisture content of the skin and make the skin soft and smooth , reduce wrinkles, has broad-spectrum antibacterial function, strong persistence, natural antibacterial function of more than 99%, and antibacterial rate of more than 80%.

有益效果:(1)、本发明中采用的微胶囊复配相变材料的芯体为正十四烷、正十六烷、正二十烷复配而成,当正十四烷、正十六烷、正二十烷按照质量比为2:4:1复配时,囊壁材料应选用机械强度和耐热性能均较优良的三聚氰胺/甲醛树脂,制得的微胶囊复配相变材料降温时,温度变化速度小,相变时间长,相变温度范围与人体舒适温度范围基本吻合,耐热性能好。 Beneficial effects: (1). The core body of the microcapsule composite phase change material used in the present invention is composed of n-tetradecane, n-hexadecane, and n-eicosane. When n-tetradecane, n-decane When hexane and n-eicosane are compounded according to the mass ratio of 2:4:1, the capsule wall material should use melamine/formaldehyde resin with excellent mechanical strength and heat resistance, and the prepared microcapsule compound phase change material When cooling down, the temperature change speed is small, the phase change time is long, the phase change temperature range basically coincides with the comfortable temperature range of the human body, and the heat resistance is good.

(2)、本发明中利用聚乙二醇对聚酰胺6进行改性,使聚酰胺6在具有自身优良性能的基础上同时兼具自调温功能,在满足运用的前提下,有改善聚酰胺6纤维的柔顺性,使其更舒适;利用低温等离子体处理涤纶纤维,将聚乙二醇接枝到涤纶纤维上,得到的改性涤纶纤维,不仅具有涤纶纤维自身的优良性能,同时提高了自身的吸湿性能,有利于对运动过程中汗液的吸收。 (2) In the present invention, polyethylene glycol is used to modify polyamide 6, so that polyamide 6 has a self-adjusting temperature function on the basis of its own excellent performance, and can improve polyamide 6 under the premise of satisfying the application. The flexibility of amide 6 fiber makes it more comfortable; use low-temperature plasma to treat polyester fiber, graft polyethylene glycol to polyester fiber, and obtain modified polyester fiber, which not only has the excellent performance of polyester fiber itself, but also improves It improves its own moisture absorption performance, which is conducive to the absorption of sweat during exercise.

(3)、通过对以上几种纤维的改性以及混纺使最后的面料充分发挥了各种纤维的优良性能弥补不足,使得制备的运动衣面料具有自动调温性、高透气性和吸汗性,使运动过程中更加舒适、安全、健康。 (3) Through the modification and blending of the above several fibers, the final fabric can give full play to the excellent properties of various fibers to make up for the shortcomings, so that the prepared sportswear fabric has automatic temperature regulation, high air permeability and sweat absorption. Make the exercise process more comfortable, safe and healthy.

(4)、将制得的预制体浸于悬浮乳液中,可以使制得的面料表面具有一层致密的抗氧化层,提高面料的耐候性;超声波处理,使悬浮乳液的有效成分均匀分散于面料的纤维中,不易散失;壳聚糖和负离子粉,具有一定的抗菌作用,使制得的面料在避免自身霉菌滋生的同时,还能够防止人体汗液的侵蚀作用,分解异味分子结构,避免运动时汗渍和污垢的异味;植物蜡作为面料的防护层,不阻碍面料的透气作用,提高面料的韧性。 (4) Immersing the prepared preform in the suspending emulsion can make the surface of the prepared fabric have a dense anti-oxidation layer and improve the weather resistance of the fabric; ultrasonic treatment makes the active ingredients of the suspending emulsion evenly dispersed in the It is not easy to lose in the fiber of the fabric; chitosan and negative ion powder have certain antibacterial effect, so that the prepared fabric can prevent the erosion of human sweat while avoiding the growth of mold itself, decompose the molecular structure of odor, and avoid exercise Sweat stains and dirt odor from time to time; Vegetable wax is used as the protective layer of the fabric, which does not hinder the breathability of the fabric and improves the toughness of the fabric.

具体实施方式 detailed description

一种自动调温透气型户外运动衣面料,由经纱和纬纱交织成预制体,将预制体浸渍后,制得面料;其中,经纱由以下重量组份的原料组成:改性锦纶纤维20-30份、改性粘胶纤维45-50份和改性聚丙烯腈纤维20-35份;纬纱由以下重量组份的原料组成:改性涤纶纤维50-60份和牛奶纤维40-50份。 An automatic temperature-regulating breathable outdoor sportswear fabric, which is interwoven with warp yarns and weft yarns to form a prefabricated body, and the prefabricated body is impregnated to obtain a fabric; wherein, the warp yarns are composed of raw materials with the following weight components: modified nylon fiber 20-30 45-50 parts of modified viscose fiber and 20-35 parts of modified polyacrylonitrile fiber; the weft yarn is composed of the following raw materials by weight: 50-60 parts of modified polyester fiber and 40-50 parts of milk fiber.

实施例1 Example 1

一种自动调温透气型户外运动衣面料的制备方法,包括以下步骤:步骤一、将重量比为2:4:1的正十四烷、正十六烷、正二十烷配置成混合溶液,将混合溶液置于三口瓶中水浴加热,水浴温度为70℃,以1300rpm的转速搅拌15min后,按照混合溶液:乳化剂:PVA水溶液=10:0.2:1.0的重量比,加入乳化剂和PVA水溶液,以450rpm的转速搅拌1.5h,形成乳液,然后加入浓度为10%的稀硫酸,调节乳液pH至5,备用; A method for preparing an automatic temperature-regulating breathable outdoor sportswear fabric, comprising the following steps: step 1, preparing n-tetradecane, n-hexadecane, and n-eicosane in a weight ratio of 2:4:1 into a mixed solution , put the mixed solution in a three-necked flask and heat it in a water bath. The temperature of the water bath is 70°C. After stirring for 15 minutes at a speed of 1300rpm, add the emulsifier and PVA according to the weight ratio of the mixed solution: emulsifier: PVA aqueous solution = 10:0.2:1.0 The aqueous solution was stirred at a speed of 450rpm for 1.5h to form an emulsion, and then dilute sulfuric acid with a concentration of 10% was added to adjust the pH of the emulsion to 5 and set aside;

步骤二、将摩尔比为1:5的三聚氰胺和甲醛置于圆底烧瓶中,形成溶液,于80℃密闭搅拌0.5h,然后加入浓度为15%的Na2CO3稀溶液,调节溶液的pH至10,50℃搅拌至溶液澄清透明;然后照该溶液:乳液=3:5的体积比,将该溶液加入步骤一制备的乳液中,搅拌3h,形成悬浮液,用离心机将悬浮液进行分离,离心速度为3000rpm,将离心得到的沉淀分别用乙二醇和去离子水洗涤5次,然后置于40℃烘箱中烘干12h,制得微胶囊复配相变材料,备用; Step 2. Put melamine and formaldehyde with a molar ratio of 1:5 in a round-bottomed flask to form a solution. Stir at 80°C for 0.5h, then add 15% Na 2 CO 3 dilute solution to adjust the pH of the solution Stir to 10, 50°C until the solution is clear and transparent; then according to the volume ratio of the solution:emulsion = 3:5, add the solution to the emulsion prepared in step 1, stir for 3 hours to form a suspension, and use a centrifuge to process the suspension Separation, the centrifugation speed is 3000rpm, the precipitate obtained by centrifugation is washed 5 times with ethylene glycol and deionized water respectively, and then placed in an oven at 40°C for 12 hours to prepare a microcapsule compound phase change material for future use;

步骤三、按照粘胶纺丝液95份、微胶囊复配相变材料5份的重量份数,称取粘胶纺丝液和步骤二制得的微胶囊复配相变材料,混合后经喷丝板挤出,制得改性粘胶纤维,备用; Step 3, according to the parts by weight of 95 parts of viscose spinning solution and 5 parts of microcapsule composite phase change material, take viscose spinning solution and the microcapsule composite phase change material prepared in step 2, mix and pass Spinneret is extruded, and modified viscose fiber is obtained, for subsequent use;

步骤四、按照紫外光固化丙烯酸酯粘合剂80份、微胶囊复配相变材料5份的重量份数,称取紫外光固化丙烯酸酯粘合剂和步骤二制得的微胶囊复配相变材料,混合得复合粘合剂,将复合粘合剂涂覆在聚丙烯腈纤维上,经紫外光照射,得到改性聚丙烯腈纤维,备用; Step 4, according to the parts by weight of 80 parts of UV curable acrylate adhesive and 5 parts of microcapsule composite phase change material, weigh the UV curable acrylate adhesive and the microcapsule composite phase prepared in step 2 Change the material, mix to obtain a composite adhesive, apply the composite adhesive on the polyacrylonitrile fiber, and irradiate with ultraviolet light to obtain a modified polyacrylonitrile fiber, which is ready for use;

步骤五、将涤纶纤维放入等离子体处理仪中,抽真空用氧气处理1.5h,然后将处理过的涤纶纤维直接浸渍在质量分数为35%聚乙二醇的溶液中,在25℃的温度下浸泡7h,取出晾干,然后用Ar等离子处理,处理时间为2.5min,功率为200W,压强为50Pa,处理后,用蒸馏水超声清洗8min,晾干后,制得改性涤纶纤维,备用; Step 5. Put the polyester fiber into the plasma treatment apparatus, vacuumize and treat it with oxygen for 1.5h, then directly immerse the treated polyester fiber in a solution with a mass fraction of 35% polyethylene glycol, at a temperature of 25°C Soak it down for 7 hours, take it out and dry it, then treat it with Ar plasma, the treatment time is 2.5min, the power is 200W, and the pressure is 50Pa. After the treatment, it is ultrasonically cleaned with distilled water for 8min, and after drying, the modified polyester fiber is prepared for future use;

步骤六、将聚酰胺6和聚乙二醇按照90:10的质量比置于质量分数为98%的甲酸中,在30℃的温度下搅拌2h,形成质量分数为17%的均匀纺丝液,通过静电纺丝机进行纺丝,纺丝液流速为0.4ml/h,喷嘴口径为1.2mm,得到改性锦纶纤维,备用; Step 6. Put polyamide 6 and polyethylene glycol in formic acid with a mass fraction of 98% according to a mass ratio of 90:10, and stir at a temperature of 30°C for 2 hours to form a uniform spinning solution with a mass fraction of 17%. , spinning by an electrospinning machine, the flow rate of the spinning solution is 0.4ml/h, and the diameter of the nozzle is 1.2mm to obtain modified nylon fibers, which are ready for use;

步骤七、按照所述改性锦纶纤维30份、改性粘胶纤维50份和改性聚丙烯腈纤维20份的重量份数,将步骤六制得的改性锦纶纤维、步骤三制得的改性粘胶纤维、步骤四制得的改性聚丙烯腈纤维合成轻纱;按照改性涤纶纤维60份和牛奶纤维40份的重量份数,将牛奶纤维和步骤五制得的改性涤纶纤维合成纬纱;最后将经纱和纬纱合成预制体,备用; Step 7, according to the parts by weight of 30 parts of modified nylon fibers, 50 parts of modified viscose fibers and 20 parts of modified polyacrylonitrile fibers, the modified nylon fibers obtained in step 6, the obtained The modified polyacrylonitrile fiber synthetic light yarn that modified viscose fiber, step 4 make; The fiber is synthesized into weft yarn; finally, the warp yarn and weft yarn are synthesized into a prefabricated body for standby;

步骤八、按照下列重量组份,称取各材料进行混合:壳聚糖2份、丙三醇3份、乙醇75份、植物蜡2份、负离子粉5份,制得悬浮乳液,将步骤七制得的预制体置于该悬浮乳液中,在超声波下浸渍10-14h后,取出烘干,制得运动衣面料。 Step 8, according to the following weight components, take each material and mix: 2 parts of chitosan, 3 parts of glycerol, 75 parts of ethanol, 2 parts of vegetable wax, 5 parts of negative ion powder, obtain suspoemulsion, and step 7 The prepared preform is placed in the suspoemulsion, soaked for 10-14 hours under ultrasonic waves, and then taken out and dried to obtain the sportswear fabric.

聚乙二醇(PEG)的分子质量远小于高聚物PA6,分子结构简单,因此随着PEG共混比例的提高,构成PA6/PEG纳米纤维的分子链的柔性要优于纯PA6纳米纤维,材料柔性的提高,导致共混纳米纤维的断裂伸长率提高。因此,将PEG引入PA6中制备的相变纳米纤维既具有PA6纤维的强度高、回弹性好、耐疲劳、可染性和耐腐蚀、耐虫蛀、质轻等优良性能,同时也具有PEG的吸收、储存、释放潜在热能等性能,虽然在PA6纤维中加入PEG降低纤维的断裂强度,但是仍满足服装的力学要求,同时改善了PA6纤维的柔性,更舒适,所以将PEG引入PA6纤维是服装优选的自调温材料。 The molecular weight of polyethylene glycol (PEG) is much smaller than that of the high polymer PA6, and the molecular structure is simple. Therefore, with the increase of the PEG blending ratio, the flexibility of the molecular chains constituting PA6/PEG nanofibers is better than that of pure PA6 nanofibers. The increased flexibility of the material leads to an improved elongation at break of the blended nanofibers. Therefore, the phase change nanofiber prepared by introducing PEG into PA6 not only has the excellent properties of PA6 fiber, such as high strength, good resilience, fatigue resistance, dyeability, corrosion resistance, insect resistance, and light weight, but also has the advantages of PEG. Absorption, storage, and release of potential heat energy, etc., although PEG is added to PA6 fiber to reduce the breaking strength of the fiber, it still meets the mechanical requirements of clothing, and at the same time improves the flexibility of PA6 fiber and makes it more comfortable. Therefore, introducing PEG into PA6 fiber is a good choice for clothing Preferred self-regulating material.

实施例2 Example 2

一种自动调温透气型户外运动衣面料的制备方法,包括以下步骤:步骤一、将重量比为2:4:1的正十四烷、正十六烷、正二十烷配置成混合溶液,将混合溶液置于三口瓶中水浴加热,水浴温度为80℃,以1000rpm的转速搅拌10min后,按照混合溶液:乳化剂:PVA水溶液=10:0.2:0.5的重量比,加入乳化剂和PVA水溶液,以600rpm的转速搅拌1h,形成乳液,然后加入浓度为10%的稀硫酸,调节乳液pH至4,备用; A method for preparing an automatic temperature-regulating breathable outdoor sportswear fabric, comprising the following steps: step 1, preparing n-tetradecane, n-hexadecane, and n-eicosane in a weight ratio of 2:4:1 into a mixed solution , put the mixed solution in a three-necked bottle and heat it in a water bath. The temperature of the water bath is 80 ° C. After stirring for 10 minutes at a speed of 1000 rpm, add the emulsifier and PVA according to the weight ratio of the mixed solution: emulsifier: PVA aqueous solution = 10: 0.2: 0.5 The aqueous solution was stirred at a speed of 600rpm for 1 hour to form an emulsion, and then 10% dilute sulfuric acid was added to adjust the pH of the emulsion to 4, and set aside;

步骤二、将摩尔比为1:4.5的三聚氰胺和甲醛置于圆底烧瓶中,形成溶液,于75℃密闭搅拌0.5h,然后加入浓度为10%的Na2CO3稀溶液,调节溶液的pH至9,45℃搅拌至溶液澄清透明;然后照该溶液:乳液=3:5的体积比,将该溶液加入步骤一制备的乳液中,搅拌2.5h,形成悬浮液,用离心机将悬浮液进行分离,离心速度为2500rpm,将离心得到的沉淀分别用乙二醇和去离子水洗涤3次,然后置于50℃烘箱中烘干10h,制得微胶囊复配相变材料,备用; Step 2: Put melamine and formaldehyde with a molar ratio of 1:4.5 in a round-bottomed flask to form a solution, and stir at 75°C for 0.5h, then add a 10% Na 2 CO 3 dilute solution to adjust the pH of the solution Stir to 9, 45°C until the solution is clear and transparent; then add the solution to the emulsion prepared in step 1 according to the volume ratio of the solution:emulsion = 3:5, stir for 2.5 hours to form a suspension, and use a centrifuge to dissolve the suspension Separation was carried out at a centrifugation speed of 2500 rpm, and the precipitate obtained by centrifugation was washed three times with ethylene glycol and deionized water respectively, and then dried in an oven at 50°C for 10 hours to obtain a microcapsule compound phase change material for future use;

步骤三、按照粘胶纺丝液90份、微胶囊复配相变材料10份的重量份数,称取粘胶纺丝液和步骤二制得的微胶囊复配相变材料,混合后经喷丝板挤出,制得改性粘胶纤维,备用; Step 3, according to the parts by weight of 90 parts of viscose spinning solution and 10 parts of microcapsule composite phase change material, take viscose spinning solution and the microcapsule composite phase change material prepared in step 2, mix and pass Spinneret is extruded, and modified viscose fiber is obtained, for subsequent use;

步骤四、按照紫外光固化丙烯酸酯粘合剂70份、微胶囊复配相变材料7份的重量份数,称取紫外光固化丙烯酸酯粘合剂和步骤二制得的微胶囊复配相变材料,混合得复合粘合剂,将复合粘合剂涂覆在聚丙烯腈纤维上,经紫外光照射,得到改性聚丙烯腈纤维,备用; Step 4, according to the parts by weight of 70 parts of UV curable acrylate adhesive and 7 parts of microcapsule composite phase change material, weigh the UV curable acrylate adhesive and the microcapsule composite phase prepared in step 2 Change the material, mix to obtain a composite adhesive, apply the composite adhesive on the polyacrylonitrile fiber, and irradiate with ultraviolet light to obtain a modified polyacrylonitrile fiber, which is ready for use;

步骤五、将涤纶纤维放入等离子体处理仪中,抽真空用氧气处理0.5h,然后将处理过的涤纶纤维直接浸渍在质量分数为20%聚乙二醇的溶液中,在25℃的温度下浸泡7h,取出晾干,然后用Ar等离子处理,处理时间为1min,功率为100W,压强为50Pa,处理后,用蒸馏水超声清洗6min,晾干后,制得改性涤纶纤维,备用; Step 5. Put the polyester fiber into the plasma treatment apparatus, vacuumize it and treat it with oxygen for 0.5h, then directly immerse the treated polyester fiber in a solution with a mass fraction of 20% polyethylene glycol, at a temperature of 25°C Soak it down for 7 hours, take it out and dry it, then treat it with Ar plasma, the treatment time is 1min, the power is 100W, and the pressure is 50Pa. After the treatment, it is ultrasonically cleaned with distilled water for 6min, and after drying, the modified polyester fiber is prepared for future use;

步骤六、将聚酰胺6和聚乙二醇按照50:50的质量比置于质量分数为98%的甲酸中,在30℃的温度下搅拌1.5h,形成质量分数为14%的均匀纺丝液,通过静电纺丝机进行纺丝,纺丝液流速为0.2ml/h,喷嘴口径为1mm,得到改性锦纶纤维,备用; Step 6. Put polyamide 6 and polyethylene glycol in formic acid with a mass fraction of 98% according to a mass ratio of 50:50, and stir at a temperature of 30°C for 1.5 hours to form a uniform spinning with a mass fraction of 14%. Liquid, spinning by electrospinning machine, spinning liquid flow rate is 0.2ml/h, nozzle aperture is 1mm, obtains modified nylon fiber, standby;

步骤七、按照所述改性锦纶纤维20份、改性粘胶纤维45份和改性聚丙烯腈纤维35份的重量份数,将步骤六制得的改性锦纶纤维、步骤三制得的改性粘胶纤维、步骤四制得的改性聚丙烯腈纤维合成轻纱;按照改性涤纶纤维50份和牛奶纤维40份的重量份数,将牛奶纤维和步骤五制得的改性涤纶纤维合成纬纱;最后将经纱和纬纱合成预制体,备用; Step 7, according to the parts by weight of 20 parts of the modified nylon fiber, 45 parts of the modified viscose fiber and 35 parts of the modified polyacrylonitrile fiber, the modified nylon fiber made in the step 6, the made in the step 3 The modified polyacrylonitrile fiber synthetic light yarn that modified viscose fiber, step 4 makes; The fiber is synthesized into weft yarn; finally, the warp yarn and weft yarn are synthesized into a prefabricated body for standby;

步骤八、按照下列重量组份,称取各材料进行混合:壳聚糖2份、丙三醇2份、乙醇60份、植物蜡2份、负离子粉1份,制得悬浮乳液,将步骤七制得的预制体置于该悬浮乳液中,在超声波下浸渍10h后,取出烘干,制得运动衣面料。 Step 8, according to the following weight components, take each material and mix: 2 parts of chitosan, 2 parts of glycerin, 60 parts of ethanol, 2 parts of vegetable wax, 1 part of negative ion powder, make suspoemulsion, and step 7 The prepared preform is placed in the suspoemulsion, soaked for 10 hours under ultrasonic waves, and then taken out and dried to obtain a sportswear fabric.

实施例3 Example 3

一种自动调温透气型户外运动衣面料的制备方法,包括以下步骤:步骤一、将重量比为2:4:1的正十四烷、正十六烷、正二十烷配置成混合溶液,将混合溶液置于三口瓶中水浴加热,水浴温度为76℃,以1100rpm的转速搅拌12min后,按照混合溶液:乳化剂:PVA水溶液=10:0.2:0.7的重量比,加入乳化剂和PVA水溶液,以550rpm的转速搅拌1.3h,形成乳液,然后加入浓度为10%的稀硫酸,调节乳液pH至4,备用; A method for preparing an automatic temperature-regulating breathable outdoor sportswear fabric, comprising the following steps: step 1, preparing n-tetradecane, n-hexadecane, and n-eicosane in a weight ratio of 2:4:1 into a mixed solution , put the mixed solution in a three-necked flask and heat it in a water bath, the temperature of the water bath is 76°C, and after stirring for 12 minutes at a speed of 1100rpm, add the emulsifier and PVA according to the weight ratio of the mixed solution: emulsifier: PVA aqueous solution = 10:0.2:0.7 The aqueous solution was stirred at a speed of 550rpm for 1.3h to form an emulsion, and then dilute sulfuric acid with a concentration of 10% was added to adjust the pH of the emulsion to 4, and set aside;

步骤二、将摩尔比为1:4.6的三聚氰胺和甲醛置于圆底烧瓶中,形成溶液,于77℃密闭搅拌0.5h,然后加入浓度为13%的Na2CO3稀溶液,调节溶液的pH至9,47℃搅拌至溶液澄清透明;然后照该溶液:乳液=3:5的体积比,将该溶液加入步骤一制备的乳液中,搅拌2.6h,形成悬浮液,用离心机将悬浮液进行分离,离心速度为2800rpm,将离心得到的沉淀分别用乙二醇和去离子水洗涤4次,然后置于45℃烘箱中烘干11.5h,制得微胶囊复配相变材料,备用; Step 2: Put melamine and formaldehyde with a molar ratio of 1:4.6 in a round-bottomed flask to form a solution, and stir at 77°C for 0.5h, then add a 13% Na 2 CO 3 dilute solution to adjust the pH of the solution Stir to 9, 47°C until the solution is clear and transparent; then add the solution to the emulsion prepared in step 1 according to the volume ratio of the solution:emulsion = 3:5, stir for 2.6 hours to form a suspension, and use a centrifuge to dissolve the suspension Separation was carried out at a centrifugation speed of 2800rpm, and the precipitate obtained by centrifugation was washed 4 times with ethylene glycol and deionized water respectively, and then placed in an oven at 45°C for 11.5 hours to obtain a microcapsule compound phase change material for future use;

步骤三、按照粘胶纺丝液92份、微胶囊复配相变材料9份的重量份数,称取粘胶纺丝液和步骤二制得的微胶囊复配相变材料,混合后经喷丝板挤出,制得改性粘胶纤维,备用; Step 3, according to the parts by weight of 92 parts of viscose spinning solution and 9 parts of microcapsule composite phase change material, take viscose spinning solution and the microcapsule composite phase change material prepared in step 2, mix and pass through Spinneret is extruded, and modified viscose fiber is obtained, for subsequent use;

步骤四、按照紫外光固化丙烯酸酯粘合剂75份、微胶囊复配相变材料6份的重量份数,称取紫外光固化丙烯酸酯粘合剂和步骤二制得的微胶囊复配相变材料,混合得复合粘合剂,将复合粘合剂涂覆在聚丙烯腈纤维上,经紫外光照射,得到改性聚丙烯腈纤维,备用; Step 4, according to the parts by weight of 75 parts of UV curable acrylate adhesive and 6 parts of microcapsule composite phase change material, weigh the UV curable acrylate adhesive and the microcapsule composite phase prepared in step 2 Change the material, mix to obtain a composite adhesive, apply the composite adhesive on the polyacrylonitrile fiber, and irradiate with ultraviolet light to obtain a modified polyacrylonitrile fiber, which is ready for use;

步骤五、将涤纶纤维放入等离子体处理仪中,抽真空用氧气处理1.1h,然后将处理过的涤纶纤维直接浸渍在质量分数为29%聚乙二醇的溶液中,在27℃的温度下浸泡6.3h,取出晾干,然后用Ar等离子处理,处理时间为2min,功率为160W,压强为56Pa,处理后,用蒸馏水超声清洗7min,晾干后,制得改性涤纶纤维,备用; Step 5. Put the polyester fiber into the plasma treatment apparatus, vacuumize and treat it with oxygen for 1.1h, then directly immerse the treated polyester fiber in a solution with a mass fraction of 29% polyethylene glycol, at a temperature of 27°C After soaking for 6.3 hours, take it out and dry it, then treat it with Ar plasma, the treatment time is 2min, the power is 160W, and the pressure is 56Pa. After the treatment, it is ultrasonically cleaned with distilled water for 7min, and after drying, the modified polyester fiber is prepared for future use;

步骤六、将聚酰胺6和聚乙二醇按照70:30的质量比置于质量分数为98%的甲酸中,在35℃的温度下搅拌1.6h,形成质量分数为15%的均匀纺丝液,通过静电纺丝机进行纺丝,纺丝液流速为0.3ml/h,喷嘴口径为1.1mm,得到改性锦纶纤维,备用; Step 6. Put polyamide 6 and polyethylene glycol in formic acid with a mass fraction of 98% according to the mass ratio of 70:30, and stir at a temperature of 35°C for 1.6h to form a uniform spinning with a mass fraction of 15%. Liquid, spinning by electrospinning machine, spinning liquid flow rate is 0.3ml/h, nozzle aperture is 1.1mm, obtains modified nylon fiber, standby;

步骤七、按照所述改性锦纶纤维25份、改性粘胶纤维42份和改性聚丙烯腈纤维28份的重量份数,将步骤六制得的改性锦纶纤维、步骤三制得的改性粘胶纤维、步骤四制得的改性聚丙烯腈纤维合成轻纱;按照改性涤纶纤维54份和牛奶纤维46份的重量份数,将牛奶纤维和步骤五制得的改性涤纶纤维合成纬纱;最后将经纱和纬纱合成预制体,备用; Step 7, according to the parts by weight of 25 parts of the modified nylon fiber, 42 parts of the modified viscose fiber and 28 parts of the modified polyacrylonitrile fiber, the modified nylon fiber made in the step 6, the made in the step 3 The modified polyacrylonitrile fiber synthetic light yarn that modified viscose fiber, step 4 makes; According to the parts by weight of 54 parts of modified polyester fiber and 46 parts of milk fiber, the modified polyester made of milk fiber and step 5 The fiber is synthesized into weft yarn; finally, the warp yarn and weft yarn are synthesized into a prefabricated body for standby;

步骤八、按照下列重量组份,称取各材料进行混合:壳聚糖2-5份、丙三醇2.5份、乙醇67份、植物蜡2.2份、负离子粉3.2份,制得悬浮乳液,将步骤七制得的预制体置于该悬浮乳液中,在超声波下浸渍12h后,取出烘干,制得运动衣面料。 Step 8, according to the following weight components, each material is weighed and mixed: 2-5 parts of chitosan, 2.5 parts of glycerol, 67 parts of ethanol, 2.2 parts of vegetable wax, 3.2 parts of negative ion powder, obtained suspoemulsion, and The prefabricated body prepared in step 7 is placed in the suspoemulsion, soaked under ultrasonic waves for 12 hours, and then taken out and dried to obtain a sportswear fabric.

Claims (5)

1.一种自动调温透气型户外运动衣面料,其特征在于:由经纱和纬纱交织成预制体,将预制体浸渍后,制得面料;其中,经纱由以下重量组份的原料组成:改性锦纶纤维20-30份、改性粘胶纤维45-50份和改性聚丙烯腈纤维20-35份;纬纱由以下重量组份的原料组成:改性涤纶纤维50-60份和牛奶纤维40-50份。 1. An automatic temperature-regulating breathable outdoor sportswear fabric, characterized in that: warp yarns and weft yarns are interwoven into a prefabricated body, and after the prefabricated body is impregnated, the fabric is obtained; wherein the warp yarns are composed of raw materials of the following weight components: 20-30 parts of permanent nylon fiber, 45-50 parts of modified viscose fiber and 20-35 parts of modified polyacrylonitrile fiber; the weft yarn is composed of the following raw materials by weight: 50-60 parts of modified polyester fiber and milk fiber 40-50 servings. 2.根据权利要求1所述的一种自动调温透气型户外运动衣面料,其特征在于:所述的改性锦纶纤维为聚乙二醇接枝聚酰胺6,其中,聚乙二醇分子量为4000-6000。 2. A kind of automatic temperature-regulating breathable outdoor sportswear fabric according to claim 1, characterized in that: the modified nylon fiber is polyethylene glycol grafted polyamide 6, wherein the polyethylene glycol molecular weight For 4000-6000. 3.根据权利要求1所述的一种自动调温透气型户外运动衣面料,其特征在于:所述的改性粘胶纤维由以下重量组份的原料组成:粘胶纺丝液90-95份,微胶囊复配相变材料5-10份。 3. A kind of automatic temperature-regulating breathable outdoor sportswear fabric according to claim 1, characterized in that: the modified viscose fiber is made up of the raw materials of the following weight components: viscose spinning solution 90-95 parts, 5-10 parts of microcapsule compound phase change materials. 4.根据权利要求1所述的一种自动调温透气型户外运动衣面料,其特征在于:所述的改性涤纶纤维为聚乙二醇接枝聚对苯二甲酸乙二醇酯,其中,聚乙二醇分子量为1000-2000。 4. A kind of automatic temperature-regulating breathable outdoor sportswear fabric according to claim 1, characterized in that: the modified polyester fiber is polyethylene glycol grafted polyethylene terephthalate, wherein , The molecular weight of polyethylene glycol is 1000-2000. 5.根据权利要求1所述的一种自动调温透气型户外运动衣面料的制备方法,其特征在于,包括以下步骤: 5. the preparation method of a kind of automatic temperature-regulating breathable type outdoor sportswear fabric according to claim 1, is characterized in that, comprises the following steps: 步骤一、将重量比为2:4:1的正十四烷、正十六烷、正二十烷配置成混合溶液,将混合溶液置于三口瓶中水浴加热,水浴温度为70-80℃,以1000-1300rpm的转速搅拌10-15min后,按照混合溶液:乳化剂:PVA水溶液=10:0.2:0.5-1.0的重量比,加入乳化剂和PVA水溶液,以450-600rpm的转速搅拌1-1.5h,形成乳液,然后加入浓度为10%的稀硫酸,调节乳液pH至4-5,备用; Step 1. Prepare n-tetradecane, n-hexadecane, and n-eicosane with a weight ratio of 2:4:1 to form a mixed solution, place the mixed solution in a three-necked bottle and heat it in a water bath, and the temperature of the water bath is 70-80°C , after stirring at a speed of 1000-1300rpm for 10-15min, according to the weight ratio of mixed solution: emulsifier: PVA aqueous solution = 10:0.2:0.5-1.0, add emulsifier and PVA aqueous solution, and stir at a speed of 450-600rpm for 1- 1.5h to form an emulsion, then add dilute sulfuric acid with a concentration of 10%, adjust the pH of the emulsion to 4-5, and set aside; 步骤二、将摩尔比为1:4.5-5的三聚氰胺和甲醛置于容器中形成溶液,于75-80℃密闭搅拌0.5h,然后加入浓度为10-15%的Na2CO3稀溶液,调节溶液的pH至9-10,45-50℃搅拌至溶液澄清透明;然后按照该溶液:乳液=3:5的体积比,将该溶液加入步骤一制备的乳液中,搅拌2.5-3h,形成悬浮液,用离心机将悬浮液进行分离,离心速度为2500-3000rpm,将离心得到的沉淀分别用乙二醇和去离子水洗涤3-5次,然后置于40-50℃烘箱中烘干10-12h,制得微胶囊复配相变材料,备用; Step 2: Put melamine and formaldehyde with a molar ratio of 1:4.5-5 in a container to form a solution, and stir in a sealed container at 75-80°C for 0.5h, then add a diluted Na 2 CO 3 solution with a concentration of 10-15%, and adjust The pH of the solution is 9-10, and stirred at 45-50°C until the solution is clear and transparent; then according to the volume ratio of the solution:emulsion=3:5, add the solution to the emulsion prepared in step 1, stir for 2.5-3h, and form a suspension Separate the suspension with a centrifuge at a speed of 2500-3000rpm, wash the precipitate obtained by centrifugation with ethylene glycol and deionized water for 3-5 times, and then dry it in an oven at 40-50°C for 10- 12h, the microcapsule composite phase change material was prepared and set aside; 步骤三、按照粘胶纺丝液90-95份、微胶囊复配相变材料5-10份的重量份数,称取粘胶纺丝液和步骤二制得的微胶囊复配相变材料,混合后经喷丝板挤出,制得改性粘胶纤维,备用; Step 3, according to the parts by weight of 90-95 parts of viscose spinning solution and 5-10 parts of microcapsule compound phase change material, weigh the viscose spinning solution and the microcapsule compound phase change material prepared in step 2 , mixed and extruded through a spinneret to obtain a modified viscose fiber for subsequent use; 步骤四、按照紫外光固化丙烯酸酯粘合剂70-80份、微胶囊复配相变材料5-7份的重量份数,称取紫外光固化丙烯酸酯粘合剂和步骤二制得的微胶囊复配相变材料,混合得复合粘合剂,将复合粘合剂涂覆在聚丙烯腈纤维上,经紫外光照射,得到改性聚丙烯腈纤维,备用; Step 4, according to the parts by weight of 70-80 parts of UV-curable acrylate adhesive and 5-7 parts of microcapsule composite phase-change material, weigh the UV-curable acrylate adhesive and the microcapsule prepared in step 2. Capsules are compounded with phase change materials, mixed to obtain a composite adhesive, coated on the polyacrylonitrile fiber by the composite adhesive, and irradiated with ultraviolet light to obtain a modified polyacrylonitrile fiber, which is ready for use; 步骤五、将涤纶纤维放入等离子体处理仪中,抽真空用氧气处理0.5-1.5h,然后将处理过的涤纶纤维直接浸渍在质量分数为20-35%聚乙二醇的溶液中,在25-30℃的温度下浸泡6-7h,取出晾干,然后用Ar等离子处理,处理时间为1-2.5min,功率为100-200W,压强为50-60Pa,处理后,用蒸馏水超声清洗6-8min,晾干后,制得改性涤纶纤维,备用; Step 5. Put the polyester fiber into the plasma treatment apparatus, vacuumize and treat it with oxygen for 0.5-1.5h, and then directly immerse the treated polyester fiber in a solution with a mass fraction of 20-35% polyethylene glycol. Soak at a temperature of 25-30°C for 6-7h, take it out and dry it, and then treat it with Ar plasma, the treatment time is 1-2.5min, the power is 100-200W, and the pressure is 50-60Pa. After treatment, it is ultrasonically cleaned with distilled water for 6 -8min, after drying, the modified polyester fiber is obtained, which is for subsequent use; 步骤六、将聚酰胺6和聚乙二醇按照50-90:10-50的质量比置于质量分数为98%的甲酸中,在30-40℃的温度下搅拌1.5-2h,形成质量分数为14-17%的均匀纺丝液,通过静电纺丝机进行纺丝,纺丝液流速为0.2-0.4ml/h,喷嘴口径为1-1.2mm,得到改性锦纶纤维,备用; Step six, polyamide 6 and polyethylene glycol are placed in formic acid with a mass fraction of 98% according to the mass ratio of 50-90:10-50, and stirred at a temperature of 30-40°C for 1.5-2h to form a mass fraction It is 14-17% uniform spinning solution, which is spun by an electrospinning machine. The flow rate of the spinning solution is 0.2-0.4ml/h, and the nozzle diameter is 1-1.2mm, so as to obtain modified nylon fiber and set aside; 步骤七、按照所述改性锦纶纤维20-30份、改性粘胶纤维45-50份和改性聚丙烯腈纤维20-35份的重量份数,将步骤六制得的改性锦纶纤维、步骤三制得的改性粘胶纤维、步骤四制得的改性聚丙烯腈纤维合成轻纱;按照改性涤纶纤维50-60份和牛奶纤维40-50份的重量份数,将牛奶纤维和步骤五制得的改性涤纶纤维合成纬纱;最后将经纱和纬纱合成预制体,备用; Step 7, according to the parts by weight of 20-30 parts of modified nylon fiber, 45-50 parts of modified viscose fiber and 20-35 parts of modified polyacrylonitrile fiber, the modified nylon fiber obtained in step 6 , the modified viscose fiber that step 3 makes, the modified polyacrylonitrile fiber synthetic light yarn that step 4 makes; According to the parts by weight of 50-60 parts of modified polyester fiber and 40-50 parts of milk fiber, milk The fiber and the modified polyester fiber prepared in step 5 synthesize the weft yarn; finally, the warp yarn and the weft yarn are synthesized into a prefabricated body for subsequent use; 步骤八、按照下列重量组份,称取各材料进行混合:壳聚糖2-5份、丙三醇2-3份、乙醇60-75份、植物蜡2-2.5份、负离子粉1-5份,制得悬浮乳液,将步骤七制得的预制体置于该悬浮乳液中,在超声波下浸渍10-14h后,取出烘干,制得运动衣面料。 Step 8, according to the following weight components, weigh each material and mix: 2-5 parts of chitosan, 2-3 parts of glycerol, 60-75 parts of ethanol, 2-2.5 parts of vegetable wax, 1-5 parts of negative ion powder part to prepare a suspoemulsion, place the prefabricated body prepared in step 7 in the suspoemulsion, immerse it under ultrasonic waves for 10-14 hours, take it out and dry it, and obtain a sportswear fabric.
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