CN117265737A - A breathable antibacterial fabric - Google Patents
A breathable antibacterial fabric Download PDFInfo
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- CN117265737A CN117265737A CN202311213336.1A CN202311213336A CN117265737A CN 117265737 A CN117265737 A CN 117265737A CN 202311213336 A CN202311213336 A CN 202311213336A CN 117265737 A CN117265737 A CN 117265737A
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- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
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- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
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- D06M2101/16—Synthetic fibres, other than mineral fibres
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Abstract
Description
技术领域Technical field
本发明涉及服饰面料技术领域,具体涉及一种透气抗菌面料。The invention relates to the technical field of clothing fabrics, and in particular to a breathable antibacterial fabric.
背景技术Background technique
随着人民生活水平的提升,人们对衣服面料的要求越来越高,涤纶面料因具有优异的弹性、抗皱性、保形性和耐穿性等优点而广泛应用在内衣内裤、婚纱、晚礼服、运动服饰等服饰上,但涤纶分子中含有的刚性苯环使其分子链易保持线型,导致涤纶面料手感较硬、触感差,针对这一问题,公开号为CN103556494B的发明专利公开了一种耐久性易护理细旦中空涤纶仿真丝梭织物制品,在后处理液中加入了聚酯聚醚有机硅三元共聚型亲水柔软整理剂,利用其中的聚硅氧烷链段赋予针织物较好的柔软性,因此,使用柔软整理剂对涤纶进行柔软整理逐渐成为较为常用的方法。With the improvement of people's living standards, people have higher and higher requirements for clothing fabrics. Polyester fabrics are widely used in underwear, wedding dresses, evening dresses because of their excellent elasticity, wrinkle resistance, shape retention and durability. , sportswear and other clothing, but the rigid benzene ring contained in the polyester molecule makes the molecular chain easy to maintain a linear shape, causing the polyester fabric to feel hard and have a poor touch. To address this problem, an invention patent with the publication number CN103556494B has disclosed a A kind of durable and easy-care fine-denier hollow polyester imitation silk woven product. A polyester polyether silicone ternary copolymer hydrophilic softening finishing agent is added to the post-treatment liquid, and the polysiloxane segments are used to give the knitted fabric Better softness, therefore, using softening finishing agents to soften polyester has gradually become a more common method.
在夏季,天气较为炎热,人们在运动时,皮肤与衣服之间舒适的微气候环境被破坏,很容易大汗淋漓,使得汗液粘在皮肤表面,产生黏腻感,而排出的汗液在适宜的温度下为细菌的繁殖提供了有利的环境,导致细菌大量繁殖,产生异味,但是,涤纶的吸湿性较差,其分子中除了两端的羟基外,没有其他极性基团,因此很难吸附汗液,且涤纶的透气性也较差,这会导致残留在皮肤表面的汗液很难快速蒸发到空气中,造成衣服的穿着体验感不佳,因此,对涤纶面料进行性能改善成为当前一个十分重要的研究方向。In summer, the weather is relatively hot. When people exercise, the comfortable microclimate environment between the skin and clothes is destroyed, and it is easy to sweat profusely, causing the sweat to stick to the surface of the skin, causing a sticky feeling. Temperature provides a favorable environment for the reproduction of bacteria, causing bacteria to multiply and produce odor. However, polyester has poor hygroscopicity. Except for the hydroxyl groups at both ends, there are no other polar groups in its molecules, so it is difficult to absorb sweat. , and the breathability of polyester is also poor, which will make it difficult for the sweat remaining on the skin surface to evaporate quickly into the air, resulting in a poor wearing experience. Therefore, improving the performance of polyester fabrics has become a very important issue at present. research direction.
公开号为CN110983585B的发明专利公开了一种户外运动针织面料的生产工艺,通过一系列的织造工艺使织造的面料带网眼,增强面料的透气性,改善了传统涤纶吸湿、散湿效果差的问题,并且在后整理的过程中使用吸湿排汗整理剂进一步提高面料的吸湿排汗性能,但是这仅解决了涤纶面料吸湿排汗性能差的问题,对于因汗液残留带来的细菌滋生问题未能改善,基于此,本发明提供了一种透气抗菌面料,通过对面料中的纤维进行改性,不仅改善了面料的吸湿排汗性能,还有效提高其抗菌性能,对提升服饰面料的舒适度具有重要意义。The invention patent with publication number CN110983585B discloses a production process for outdoor sports knitted fabrics. Through a series of weaving processes, the woven fabrics are meshed, which enhances the breathability of the fabrics and improves the problem of poor moisture absorption and moisture dissipation effects of traditional polyester. , and use moisture-wicking finishing agents in the post-finishing process to further improve the moisture-wicking performance of the fabric, but this only solves the problem of poor moisture-wicking performance of polyester fabrics, and fails to solve the problem of bacterial growth caused by sweat residue. Improvement. Based on this, the present invention provides a breathable antibacterial fabric. By modifying the fibers in the fabric, it not only improves the moisture absorption and perspiration performance of the fabric, but also effectively improves its antibacterial performance, which has the effect of improving the comfort of clothing fabrics. Significance.
发明内容Contents of the invention
本发明的目的在于提供一种透气抗菌面料,解决了以下技术问题:The purpose of the present invention is to provide a breathable antibacterial fabric that solves the following technical problems:
(1)解决了涤纶面料因吸湿性、透气性差而导致的吸湿排汗性能不佳的问题;(1) Solve the problem of poor moisture absorption and perspiration performance of polyester fabrics due to poor moisture absorption and air permeability;
(2)解决了涤纶面料抗菌性能差的问题。(2) Solve the problem of poor antibacterial performance of polyester fabrics.
本发明的目的可以通过以下技术方案实现:The object of the present invention can be achieved through the following technical solutions:
一种透气抗菌面料,所述面料的制备方法包括以下步骤:A breathable antibacterial fabric. The preparation method of the fabric includes the following steps:
步骤一:将重量份为70-80份的氨酯型涤纶纤维和20-30份的季铵盐型苎麻纤维分别用纺纱机纺成纱线,再送入织造机中进行织造,形成坯布;Step 1: Spun 70-80 parts by weight of urethane-type polyester fiber and 20-30 parts by weight of quaternary ammonium salt-type ramie fiber into yarn using a spinning machine, and then feed them into a weaving machine for weaving to form a gray cloth;
步骤二:采用高压喷射溢流机对坯布进行退浆精炼处理;Step 2: Use a high-pressure jet overflow machine to desizing and refining the gray fabric;
步骤三:将处理后的坯布先进行清水浸轧,再进行定型烘干处理,得到面料层;Step 3: The treated gray fabric is first padded with clean water, and then subjected to shaping and drying treatment to obtain the fabric layer;
步骤四:将面料层置于柔软整理剂中充分振荡浸轧,进行柔软整理,烘干后得到透气抗菌面料。Step 4: Place the fabric layer in the softening finishing agent, fully vibrate and pad, perform soft finishing, and dry to obtain a breathable antibacterial fabric.
进一步优选地,步骤一中,所述氨酯型涤纶纤维的制备方法包括以下步骤:Further preferably, in step one, the preparation method of the urethane polyester fiber includes the following steps:
S1:将涤纶纤维置于质量分数为5-6%的氢氧化钠溶液中,在80-90℃水浴条件下碱处理50-60min,然后过滤、洗至中性、烘干;S1: Place the polyester fiber in a sodium hydroxide solution with a mass fraction of 5-6%, treat it with alkali in a water bath at 80-90°C for 50-60 minutes, then filter, wash until neutral, and dry;
S2:将碱处理后的涤纶纤维和1,4-二氧六环混合,再加入六亚甲基二异氰酸酯和催化剂,搅拌均匀,升高温度至60-70℃,反应4-6h,反应完成后,减压蒸馏除去溶剂,得到氨酯型涤纶纤维。S2: Mix the alkali-treated polyester fiber and 1,4-dioxane, then add hexamethylene diisocyanate and catalyst, stir evenly, raise the temperature to 60-70°C, react for 4-6 hours, and the reaction is completed Afterwards, the solvent is distilled off under reduced pressure to obtain urethane polyester fiber.
进一步优选地,步骤S2中,所述催化剂为二月桂酸二丁基锡。Further preferably, in step S2, the catalyst is dibutyltin dilaurate.
在上述技术方案中,将涤纶纤维进行碱处理时,其表面的酯基会发生水解,产生活性羟基,在二月桂酸二丁基锡的催化作用下,活性羟基可以和六亚甲基二异氰酸酯结构中的异氰酸酯基团发生交联反应,生成氨酯型涤纶纤维。In the above technical solution, when the polyester fiber is treated with alkali, the ester groups on the surface will be hydrolyzed to produce active hydroxyl groups. Under the catalytic action of dibutyltin dilaurate, the active hydroxyl groups can be combined with the hexamethylene diisocyanate structure. The isocyanate group undergoes a cross-linking reaction to produce urethane-type polyester fiber.
进一步优选地,步骤一中,所述季铵盐型苎麻纤维的制备方法包括以下步骤:Further preferably, in step one, the preparation method of the quaternary ammonium salt type ramie fiber includes the following steps:
A:将苎麻纤维置于质量分数为10-20%的氢氧化钠溶液中,在室温条件下碱处理1-2h,然后过滤、洗至中性、烘干;A: Place the ramie fiber in a sodium hydroxide solution with a mass fraction of 10-20%, treat it with alkali at room temperature for 1-2 hours, then filter, wash until neutral, and dry;
B:将碱处理后的苎麻纤维和乙醇混合,升高温度至60-70℃,再加入环氧氯丙烷和缚酸剂,反应2-3h后洗涤、烘干,得到改性苎麻纤维;B: Mix the alkali-treated ramie fiber and ethanol, raise the temperature to 60-70°C, then add epichlorohydrin and an acid-binding agent, react for 2-3 hours, wash and dry to obtain modified ramie fiber;
C:将改性苎麻纤维置于乙醇中,加入季铵化试剂,在50-60℃条件下保温反应4-5h,用冰醋酸调节pH至6-7,继续反应4-6h,除去溶剂后,洗涤、干燥,得到季铵盐型苎麻纤维。C: Place the modified ramie fiber in ethanol, add quaternizing reagent, insulate and react at 50-60°C for 4-5 hours, adjust the pH to 6-7 with glacial acetic acid, continue the reaction for 4-6 hours, and remove the solvent , washed and dried to obtain quaternary ammonium salt type ramie fiber.
进一步优选地,步骤B中,所述缚酸剂为吡啶或者三乙胺中的任意一种。Further preferably, in step B, the acid binding agent is either pyridine or triethylamine.
进一步优选地,步骤C中,所述季铵化试剂为N,N-二甲基正辛胺或者N,N-二甲基癸胺中的任意一种。Further preferably, in step C, the quaternization reagent is any one of N,N-dimethyln-octylamine or N,N-dimethyldecylamine.
在上述技术方案中,苎麻纤维碱处理后表面产生的羟基会和环氧氯丙烷中的卤素官能团发生取代反应,将环氧基团引入苎麻纤维的结构中,得到改性苎麻纤维,而后其结构中的环氧基团通过和季铵化试剂发生季铵化反应,得到季铵盐型苎麻纤维。In the above technical solution, the hydroxyl groups generated on the surface of the ramie fiber after alkali treatment will undergo a substitution reaction with the halogen functional group in epichlorohydrin, and the epoxy group will be introduced into the structure of the ramie fiber to obtain modified ramie fiber, and then its structure The epoxy group in the fiber undergoes a quaternization reaction with a quaternization reagent to obtain quaternary ammonium salt type ramie fiber.
进一步优选地,步骤二中,所述退浆精炼处理的温度为100-120℃,时间为30-40min。Further preferably, in step two, the temperature of the desizing and refining treatment is 100-120°C, and the time is 30-40 minutes.
进一步优选地,步骤四中,所述柔软整理剂为硅油或者氨基硅油中的任意一种。Further preferably, in step four, the softening finishing agent is any one of silicone oil or amino silicone oil.
本发明的有益效果:Beneficial effects of the present invention:
本发明制备的氨酯型涤纶纤维中含有大量亲水性氨酯基团,改变了涤纶分子中极性基团少的问题,有效地提高了涤纶纤维的亲水性,在人体排出汗液后,涤纶纤维会将汗液吸附在其表面,而苎麻纤维结构中有沟状空腔,管壁孔隙较多,故透气性较好,吸附在涤纶纤维表面的汗液可以将汗水通过苎麻纤维的孔隙排出,从而将汗液蒸发出去,使面料起到吸湿排汗的效果,由此保持皮肤表面的干爽,提高面料的舒适度,此外,制备的季铵盐型苎麻纤维带正电,而各类细菌通常呈现负电性,二者相互结合,会导致细菌的细胞膜破裂,抑制其增殖,从而有效提高面料的抗菌性能,避免因汗液残留在皮肤表面而引起的细菌滋生问题,减少异味产生。The urethane type polyester fiber prepared by the invention contains a large number of hydrophilic urethane groups, which changes the problem of few polar groups in the polyester molecules and effectively improves the hydrophilicity of the polyester fiber. After the human body discharges sweat, Polyester fiber will absorb sweat on its surface, while the ramie fiber structure has groove-like cavities and more pores in the tube wall, so it has better air permeability. The sweat adsorbed on the surface of the polyester fiber can discharge the sweat through the pores of the ramie fiber. Thereby the sweat evaporates out, making the fabric have the effect of moisture absorption and perspiration, thus keeping the skin surface dry and improving the comfort of the fabric. In addition, the prepared quaternary ammonium salt type ramie fiber is positively charged, and various types of bacteria usually show Negative electricity, the combination of the two will cause the cell membrane of bacteria to rupture and inhibit their proliferation, thereby effectively improving the antibacterial performance of the fabric, avoiding bacterial breeding problems caused by sweat remaining on the skin surface, and reducing the generation of odor.
当然,实施本发明的任一产品并不一定需要同时达到以上所述的所有优点。Of course, any product implementing the present invention does not necessarily need to achieve all the above-mentioned advantages at the same time.
附图说明Description of the drawings
为了更清楚地说明本发明实施例的技术方案,下面将对实施例描述所需要使用的附图作简单地介绍,显而易见地,下面描述中的附图仅仅是本发明的一些实施例,对于本领域普通技术人员来讲,在不付出创造性劳动的前提下,还可以根据这些附图获得其他的附图。In order to explain the technical solutions of the embodiments of the present invention more clearly, the drawings needed to describe the embodiments will be briefly introduced below. Obviously, the drawings in the following description are only some embodiments of the present invention. For those of ordinary skill in the art, other drawings can also be obtained based on these drawings without exerting creative efforts.
图1为本发明本发明实施例1中涤纶纤维和氨酯型涤纶纤维的红外谱图。Figure 1 is an infrared spectrum of polyester fiber and urethane type polyester fiber in Example 1 of the present invention.
图2为本发明本发明实施例1中苎麻纤维和季铵盐型苎麻纤维的红外谱图。Figure 2 is an infrared spectrum of ramie fiber and quaternary ammonium salt type ramie fiber in Example 1 of the present invention.
具体实施方式Detailed ways
下面将结合本发明实施例中的附图,对本发明实施例中的技术方案进行清楚、完整地描述,显然,所描述的实施例仅仅是本发明一部分实施例,而不是全部的实施例。基于本发明中的实施例,本领域普通技术人员在没有作出创造性劳动前提下所获得的所有其它实施例,都属于本发明保护的范围。The technical solutions in the embodiments of the present invention will be clearly and completely described below with reference to the accompanying drawings in the embodiments of the present invention. Obviously, the described embodiments are only some of the embodiments of the present invention, rather than all the embodiments. Based on the embodiments of the present invention, all other embodiments obtained by those of ordinary skill in the art without creative efforts fall within the scope of protection of the present invention.
实施例1Example 1
一、氨酯型涤纶纤维的制备1. Preparation of urethane polyester fiber
S1:将5g涤纶纤维置于120mL质量分数为5%的氢氧化钠溶液中,在80℃水浴条件下碱处理50min,然后过滤、洗至中性、烘干;S1: Place 5g polyester fiber in 120mL sodium hydroxide solution with a mass fraction of 5%, treat it with alkali in a water bath at 80°C for 50 minutes, then filter, wash until neutral, and dry;
S2:将2.6g碱处理后的涤纶纤维和60mL的1,4-二氧六环混合,再加入8.3g六亚甲基二异氰酸酯和0.2g二月桂酸二丁基锡,搅拌均匀,升高温度至60℃,反应5h,反应完成后,减压蒸馏除去溶剂,得到氨酯型涤纶纤维。S2: Mix 2.6g of alkali-treated polyester fiber and 60mL of 1,4-dioxane, then add 8.3g of hexamethylene diisocyanate and 0.2g of dibutyltin dilaurate, stir evenly, and raise the temperature to 60°C, react for 5 hours. After the reaction is completed, the solvent is distilled off under reduced pressure to obtain urethane polyester fiber.
使用美国Nicolet公司的傅里叶变换红外光谱仪对涤纶纤维和氨酯型涤纶纤维进行红外表征,波数范围为4000-500cm-1,结果如图1所示,氨酯型涤纶纤维在3318cm-1处出现N-H的特征吸收峰,在2894cm-1处出现亚甲基中C-H的特征吸收峰,在1710cm-1处出现C=0的特征吸收峰,说明涤纶纤维中的羟基和六亚甲基二异氰酸酯结构中的异氰酸酯基团发生了反应。The Fourier transform infrared spectrometer of Nicolet Company of the United States was used to conduct infrared characterization of polyester fiber and urethane polyester fiber. The wave number range is 4000-500cm -1 . The results are shown in Figure 1. The urethane polyester fiber is at 3318cm -1 The characteristic absorption peak of NH appears, the characteristic absorption peak of CH in methylene appears at 2894cm -1 , and the characteristic absorption peak of C=0 appears at 1710cm -1 , indicating that the hydroxyl and hexamethylene diisocyanate in the polyester fiber The isocyanate groups in the structure reacted.
二、季铵盐型苎麻纤维的制备2. Preparation of quaternary ammonium salt type ramie fiber
A:将3g苎麻纤维置于95mL质量分数为10%的氢氧化钠溶液中,在室温条件下碱处理2h,然后过滤、洗至中性、烘干;A: Place 3g of ramie fiber in 95mL of 10% sodium hydroxide solution, treat it with alkali at room temperature for 2 hours, then filter, wash until neutral, and dry;
B:将1.8g碱处理后的苎麻纤维和20mL乙醇混合,升高温度至60℃,再加入3.2g环氧氯丙烷和0.5g吡啶,反应3h后洗涤、烘干,得到改性苎麻纤维;B: Mix 1.8g alkali-treated ramie fiber and 20mL ethanol, raise the temperature to 60°C, then add 3.2g epichlorohydrin and 0.5g pyridine, react for 3 hours, wash and dry to obtain modified ramie fiber;
C:将0.6g改性苎麻纤维置于30mL乙醇中,加入2.2g的N,N-二甲基癸胺,在60℃条件下保温反应5h,用冰醋酸调节pH至6,继续反应4h,除去溶剂后,洗涤、干燥,得到季铵盐型苎麻纤维。C: Place 0.6g of modified ramie fiber in 30mL of ethanol, add 2.2g of N,N-dimethyldecylamine, incubate at 60°C for 5h, adjust the pH to 6 with glacial acetic acid, and continue the reaction for 4h. After removing the solvent, washing and drying are performed to obtain quaternary ammonium salt type ramie fiber.
对苎麻纤维和季铵盐型苎麻纤维进行红外表征,结果如图2所示,季铵盐型苎麻纤维在2942cm-1处出现甲基中C-H的特征吸收峰,在2907cm-1处出现亚甲基中C-H的特征吸收峰,在1465cm-1处出现季铵盐的特征吸收峰,说明改性苎麻纤维中的环氧基团和N,N-二甲基癸胺发生了季铵化反应。The infrared characterization of ramie fiber and quaternary ammonium salt type ramie fiber is shown in Figure 2. The characteristic absorption peak of CH in the methyl group appears at 2942cm -1 in the quaternary ammonium salt type ramie fiber and methylene appears at 2907cm -1 The characteristic absorption peak of CH in the base and the characteristic absorption peak of quaternary ammonium salt appear at 1465cm -1 , indicating that the quaternization reaction between the epoxy group in the modified ramie fiber and N,N-dimethyldecylamine has occurred.
三、透气抗菌面料的制备3. Preparation of breathable antibacterial fabrics
步骤一:将重量份为70份的氨酯型涤纶纤维和20份的季铵盐型苎麻纤维分别用纺纱机纺成纱线,再送入织造机中进行织造,形成坯布;Step 1: Spun 70 parts by weight of urethane-type polyester fiber and 20 parts by weight of quaternary ammonium salt-type ramie fiber into yarn using a spinning machine, and then feed them into a weaving machine for weaving to form a gray cloth;
步骤二:采用高压喷射溢流机在温度为100℃的条件下对坯布进行退浆精炼处理30min;Step 2: Use a high-pressure jet overflow machine to desizing and refining the gray fabric at a temperature of 100°C for 30 minutes;
步骤三:将处理后的坯布先进行清水浸轧,再进行定型烘干处理,得到面料层;Step 3: The treated gray fabric is first padded with clean water, and then subjected to shaping and drying treatment to obtain the fabric layer;
步骤四:将面料层置于氨基硅油中充分振荡浸轧,进行柔软整理,烘干后得到透气抗菌面料。Step 4: Place the fabric layer in amino silicone oil, fully oscillate and pad, perform soft finishing, and dry to obtain a breathable antibacterial fabric.
实施例2Example 2
步骤一:将重量份为75份的氨酯型涤纶纤维和25份的季铵盐型苎麻纤维分别用纺纱机纺成纱线,再送入织造机中进行织造,形成坯布;Step 1: Spun 75 parts by weight of urethane type polyester fiber and 25 parts by weight of quaternary ammonium salt type ramie fiber into yarn using a spinning machine, and then feed them into a weaving machine for weaving to form a gray cloth;
步骤二:采用高压喷射溢流机在温度为110℃的条件下对坯布进行退浆精炼处理35min;Step 2: Use a high-pressure jet overflow machine to desizing and refining the gray fabric at a temperature of 110°C for 35 minutes;
步骤三:将处理后的坯布先进行清水浸轧,再进行定型烘干处理,得到面料层;Step 3: The treated gray fabric is first padded with clean water, and then subjected to shaping and drying treatment to obtain the fabric layer;
步骤四:将面料层置于氨基硅油中充分振荡浸轧,进行柔软整理,烘干后得到透气抗菌面料。Step 4: Place the fabric layer in amino silicone oil, fully oscillate and pad, perform soft finishing, and dry to obtain a breathable antibacterial fabric.
实施例3Example 3
步骤一:将重量份为80份的氨酯型涤纶纤维和30份的季铵盐型苎麻纤维分别用纺纱机纺成纱线,再送入织造机中进行织造,形成坯布;Step 1: Spun 80 parts by weight of urethane-type polyester fiber and 30 parts by weight of quaternary ammonium salt-type ramie fiber into yarn using a spinning machine, and then feed them into a weaving machine for weaving to form a gray cloth;
步骤二:采用高压喷射溢流机在温度为120℃的条件下对坯布进行退浆精炼处理40min;Step 2: Use a high-pressure jet overflow machine to desizing and refining the gray fabric at a temperature of 120°C for 40 minutes;
步骤三:将处理后的坯布先进行清水浸轧,再进行定型烘干处理,得到面料层;Step 3: The treated gray fabric is first padded with clean water, and then subjected to shaping and drying treatment to obtain the fabric layer;
步骤四:将面料层置于氨基硅油中充分振荡浸轧,进行柔软整理,烘干后得到透气抗菌面料。Step 4: Place the fabric layer in amino silicone oil, fully oscillate and pad, perform soft finishing, and dry to obtain a breathable antibacterial fabric.
对比例1Comparative example 1
步骤一:将重量份为80份的氨酯型涤纶纤维用纺纱机纺成纱线,再送入织造机中进行织造,形成坯布;Step 1: Use a spinning machine to spin 80 parts by weight of urethane polyester fiber into yarn, and then feed it into a weaving machine for weaving to form a gray cloth;
步骤二:采用高压喷射溢流机在温度为120℃的条件下对坯布进行退浆精炼处理40min;Step 2: Use a high-pressure jet overflow machine to desizing and refining the gray fabric at a temperature of 120°C for 40 minutes;
步骤三:将处理后的坯布先进行清水浸轧,再进行定型烘干处理,得到面料层;Step 3: The treated gray fabric is first padded with clean water, and then subjected to shaping and drying treatment to obtain the fabric layer;
步骤四:将面料层置于氨基硅油中充分振荡浸轧,进行柔软整理,烘干后得到透气抗菌面料。Step 4: Place the fabric layer in amino silicone oil, fully oscillate and pad, perform soft finishing, and dry to obtain a breathable antibacterial fabric.
其中氨酯型涤纶纤维的制备方法同实施例1。The preparation method of urethane polyester fiber is the same as in Example 1.
对比例2Comparative example 2
步骤一:将重量份为80份的涤纶纤维和30份的季铵盐型苎麻纤维分别用纺纱机纺成纱线,再送入织造机中进行织造,形成坯布;Step 1: Spun 80 parts by weight of polyester fiber and 30 parts by weight of quaternary ammonium salt type ramie fiber into yarn using a spinning machine, and then feed them into a weaving machine for weaving to form gray cloth;
步骤二:采用高压喷射溢流机在温度为120℃的条件下对坯布进行退浆精炼处理40min;Step 2: Use a high-pressure jet overflow machine to desizing and refining the gray fabric at a temperature of 120°C for 40 minutes;
步骤三:将处理后的坯布先进行清水浸轧,再进行定型烘干处理,得到面料层;Step 3: The treated gray fabric is first padded with clean water, and then subjected to shaping and drying treatment to obtain the fabric layer;
步骤四:将面料层置于氨基硅油中充分振荡浸轧,进行柔软整理,烘干后得到透气抗菌面料。Step 4: Place the fabric layer in amino silicone oil, fully oscillate and pad, perform soft finishing, and dry to obtain a breathable antibacterial fabric.
其中季铵盐型苎麻纤维的制备方法同实施例1。The preparation method of quaternary ammonium salt type ramie fiber is the same as in Example 1.
对比例3Comparative example 3
步骤一:将重量份为80份的涤纶纤维和30份的苎麻纤维分别用纺纱机纺成纱线,再送入织造机中进行织造,形成坯布;Step 1: Spun 80 parts by weight of polyester fiber and 30 parts by weight of ramie fiber into yarn using a spinning machine, and then feed them into a weaving machine for weaving to form gray cloth;
步骤二:采用高压喷射溢流机在温度为120℃的条件下对坯布进行退浆精炼处理40min;Step 2: Use a high-pressure jet overflow machine to desizing and refining the gray fabric at a temperature of 120°C for 40 minutes;
步骤三:将处理后的坯布先进行清水浸轧,再进行定型烘干处理,得到面料层;Step 3: The treated gray fabric is first padded with clean water, and then subjected to shaping and drying treatment to obtain the fabric layer;
步骤四:将面料层置于氨基硅油中充分振荡浸轧,进行柔软整理,烘干后得到透气抗菌面料。Step 4: Place the fabric layer in amino silicone oil, fully oscillate and pad, perform soft finishing, and dry to obtain a breathable antibacterial fabric.
对比例4Comparative example 4
步骤一:将重量份为80份的涤纶纤维用纺纱机纺成纱线,再送入织造机中进行织造,形成坯布;Step 1: Use a spinning machine to spin 80 parts by weight of polyester fiber into yarn, and then feed it into a weaving machine for weaving to form a gray cloth;
步骤二:采用高压喷射溢流机在温度为120℃的条件下对坯布进行退浆精炼处理40min;Step 2: Use a high-pressure jet overflow machine to desizing and refining the gray fabric at a temperature of 120°C for 40 minutes;
步骤三:将处理后的坯布先进行清水浸轧,再进行定型烘干处理,得到面料层;Step 3: The treated gray fabric is first padded with clean water, and then subjected to shaping and drying treatment to obtain the fabric layer;
步骤四:将面料层置于氨基硅油中充分振荡浸轧,进行柔软整理,烘干后得到透气抗菌面料。Step 4: Place the fabric layer in amino silicone oil, fully oscillate and pad, perform soft finishing, and dry to obtain a breathable antibacterial fabric.
性能检测Performance testing
①、测试面料的吸湿性①. Test the hygroscopicity of fabrics
将实施例1-实施例3及对比例1-对比例4制备的面料裁剪成符合规格的试样,参照国家标准GB/T 21655.1-2008《纺织品吸湿速干性的评定第1部分:单项组合试验法》测试试样的吸水率,测试结果见下表:The fabrics prepared in Examples 1 to 3 and Comparative Examples 1 to 4 were cut into samples that met the specifications. Refer to the national standard GB/T 21655.1-2008 "Evaluation of moisture absorption and quick-drying properties of textiles - Part 1: Individual combinations" Test the water absorption rate of the sample according to the "Test Method". The test results are shown in the table below:
通过上表数据可知,实施例1-实施例3制备的面料都加入氨酯型涤纶纤维,因此吸水率较高,说明面料的吸湿性较好,对比例1制备的面料也加入具有大量亲水性基团的氨酯型涤纶纤维,故吸湿性也较好,而对比例2-对比例4制备的面料未对涤纶纤维进行亲水改性,因此面料的吸湿性较差,表现出的吸水率也较低。It can be seen from the data in the above table that the fabrics prepared in Examples 1 to 3 are all added with urethane-type polyester fibers, so the water absorption rate is higher, indicating that the fabrics have better hygroscopicity. The fabrics prepared in Comparative Example 1 are also added with a large amount of hydrophilic fibers. Urethane-type polyester fiber with sexual groups, so the hygroscopicity is also better. However, the fabrics prepared in Comparative Examples 2 to 4 did not carry out hydrophilic modification of the polyester fiber, so the hygroscopicity of the fabric was poor and the water absorption was poor. The rate is also lower.
②、测试面料的透气性② Test the breathability of the fabric
将实施例1-实施例3及对比例1-对比例4制备的面料裁剪成符合规格的试样,参照国家标准GB/T 5453-1997《纺织品织物透气性的测定》测试试样的透气率,加压压力为100Pa,温度为20℃,相对湿度为65%,测试结果见下表:The fabrics prepared in Examples 1 to 3 and Comparative Examples 1 to 4 were cut into samples that met the specifications, and the air permeability of the samples was tested with reference to the national standard GB/T 5453-1997 "Determination of Air Permeability of Textile Fabrics" , the pressurizing pressure is 100Pa, the temperature is 20°C, and the relative humidity is 65%. The test results are shown in the table below:
通过上表数据可知,实施例1-实施例3制备的面料透气率较高,因此具有良好的透气性,对比例2和对比例3制备的面料透气率比实施例1-实施例3略低,因在面料的制备过程中加入具有透气性的苎麻纤维,故面料的透气性略好,而对比例1和对比例4制备的面料均因未加入苎麻纤维,透气率都较低,因此透气性较差。It can be seen from the data in the above table that the fabrics prepared in Examples 1 to 3 have higher air permeability and therefore have good air permeability. The fabrics prepared in Comparative Examples 2 and 3 have slightly lower air permeability than those in Examples 1 to 3. , because breathable ramie fiber is added during the preparation process of the fabric, the breathability of the fabric is slightly better. However, the fabrics prepared in Comparative Example 1 and Comparative Example 4 have low air permeability because no ramie fiber is added, so the breathability is low. Poor sex.
③、测试面料的抗菌性能③. Test the antibacterial properties of fabrics
将实施例1-实施例3及对比例1-对比例4制备的面料裁剪成符合规格的试样,参照国家标准GB/T 20944.3-2008《纺织品抗菌性能的评价第3部分:振荡法》测试试样的抗菌性能,选择金黄色葡萄球菌作为测试菌种,测试结果见下表:The fabrics prepared in Examples 1 to 3 and Comparative Examples 1 to 4 were cut into samples that met the specifications, and tested with reference to the national standard GB/T 20944.3-2008 "Evaluation of Antibacterial Performance of Textiles Part 3: Oscillation Method" For the antibacterial properties of the sample, Staphylococcus aureus was selected as the test strain. The test results are shown in the table below:
通过上表数据可知,实施例1-实施例3制备的面料都因加入季铵盐型苎麻纤维,表现出优异的抗菌性能,对比例2制备的面料抗菌率比实施例1-实施例3略低,因将季铵盐型苎麻纤维加入到面料的制备过程中,故抗菌性能相对也较好,而对比例1、对比例3和对比例4制备的面料因未加入季铵盐型苎麻纤维,抗菌率较低,抗菌性能较差。It can be seen from the data in the above table that the fabrics prepared in Examples 1 to 3 all show excellent antibacterial properties due to the addition of quaternary ammonium salt type ramie fibers. The antibacterial rate of the fabrics prepared in Comparative Example 2 is slightly higher than that in Examples 1 to 3. Low, because the quaternary ammonium salt type ramie fiber was added to the fabric preparation process, the antibacterial performance is relatively good, while the fabrics prepared in Comparative Example 1, Comparative Example 3 and Comparative Example 4 did not add the quaternary ammonium salt type ramie fiber. , the antibacterial rate is low and the antibacterial performance is poor.
在本说明书的描述中,参考术语“一个实施例”、“一些实施例”、“示例”、“具体示例”、或“一些示例”等的描述意指结合该实施例或示例描述的具体特征、结构、材料或者特点包含于本发明的至少一个实施例或示例中。在本说明书中,对上述术语的示意性表述不必须针对的是相同的实施例或示例。而且,描述的具体特征、结构、材料或者特点可以在任一个或多个实施例或示例中以合适的方式结合。此外,在不相互矛盾的情况下,本领域的技术人员可以将本说明书中描述的不同实施例或示例以及不同实施例或示例的特征进行结合和组合。In the description of this specification, reference to the terms "one embodiment," "some embodiments," "an example," "specific examples," or "some examples" or the like means that specific features are described in connection with the embodiment or example. , structures, materials or features are included in at least one embodiment or example of the invention. In this specification, the schematic expressions of the above terms are not necessarily directed to the same embodiment or example. Furthermore, the specific features, structures, materials or characteristics described may be combined in any suitable manner in any one or more embodiments or examples. Furthermore, those skilled in the art may combine and combine different embodiments or examples and features of different embodiments or examples described in this specification unless they are inconsistent with each other.
以上内容仅仅是对本发明的构思所作的举例和说明,所属本技术领域的技术人员对所描述的具体实施例做各种各样的修改或补充或采用类似的方式替代,只要不偏离发明的构思或者超越本权利要求书所定义的范围,均应属于本发明的保护范围。The above contents are only examples and explanations of the concept of the invention. Those skilled in the art may make various modifications or additions to the described specific embodiments or substitute them in similar ways, as long as they do not deviate from the concept of the invention. or beyond the scope defined by the claims, shall belong to the protection scope of the present invention.
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN118326597A (en) * | 2024-04-11 | 2024-07-12 | 潮州市丹辉婚纱礼服有限公司 | A weaving method for skin-friendly and breathable fabric |
| CN119711027A (en) * | 2025-02-28 | 2025-03-28 | 上海幼岚纺织科技有限公司 | Moisture-absorbing antibacterial fabric and preparation method thereof |
Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101225602A (en) * | 2007-12-18 | 2008-07-23 | 苏州大学 | Graft Amination Modification Technology of Hemp Fiber |
| CN103173917A (en) * | 2013-03-28 | 2013-06-26 | 江苏新凯盛企业发展有限公司 | Hydrophilic and easy-decontamination terylene fabrics and preparation method thereof |
| KR101428688B1 (en) * | 2013-03-21 | 2014-08-11 | 주식회사 제너럴아웃피터스 | Functional PET yarn and its manufacturing method |
| CN106480741A (en) * | 2016-09-22 | 2017-03-08 | 广州大学 | A kind of method for sorting of multifunctional textile product |
| CN111041626A (en) * | 2019-12-03 | 2020-04-21 | 朱佳乐 | Preparation method of breathable antibacterial close-fitting sportswear fabric |
| CN113403845A (en) * | 2021-06-28 | 2021-09-17 | 界首市华宇纺织有限公司 | Production process of antibacterial yarn |
| CN114434909A (en) * | 2022-02-23 | 2022-05-06 | 安徽弋尚纺织科技有限公司 | High-flame-retardance breathable protective fabric and preparation method thereof |
| WO2022213541A1 (en) * | 2021-04-07 | 2022-10-13 | 罗莱生活科技股份有限公司 | Anti-microbial textile and preparation method therefor |
| CN115434062A (en) * | 2022-10-08 | 2022-12-06 | 仙桃市融祥无纺布制品有限公司 | Preparation method of moisture-absorbing sweat-releasing antibacterial fabric |
| CN116163054A (en) * | 2023-04-26 | 2023-05-26 | 比音勒芬服饰股份有限公司 | High-elasticity breathable three-dimensional knitwear fabric and preparation method thereof |
-
2023
- 2023-09-20 CN CN202311213336.1A patent/CN117265737B/en active Active
Patent Citations (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101225602A (en) * | 2007-12-18 | 2008-07-23 | 苏州大学 | Graft Amination Modification Technology of Hemp Fiber |
| KR101428688B1 (en) * | 2013-03-21 | 2014-08-11 | 주식회사 제너럴아웃피터스 | Functional PET yarn and its manufacturing method |
| CN103173917A (en) * | 2013-03-28 | 2013-06-26 | 江苏新凯盛企业发展有限公司 | Hydrophilic and easy-decontamination terylene fabrics and preparation method thereof |
| CN106480741A (en) * | 2016-09-22 | 2017-03-08 | 广州大学 | A kind of method for sorting of multifunctional textile product |
| CN111041626A (en) * | 2019-12-03 | 2020-04-21 | 朱佳乐 | Preparation method of breathable antibacterial close-fitting sportswear fabric |
| WO2022213541A1 (en) * | 2021-04-07 | 2022-10-13 | 罗莱生活科技股份有限公司 | Anti-microbial textile and preparation method therefor |
| CN113403845A (en) * | 2021-06-28 | 2021-09-17 | 界首市华宇纺织有限公司 | Production process of antibacterial yarn |
| CN114434909A (en) * | 2022-02-23 | 2022-05-06 | 安徽弋尚纺织科技有限公司 | High-flame-retardance breathable protective fabric and preparation method thereof |
| CN115434062A (en) * | 2022-10-08 | 2022-12-06 | 仙桃市融祥无纺布制品有限公司 | Preparation method of moisture-absorbing sweat-releasing antibacterial fabric |
| CN116163054A (en) * | 2023-04-26 | 2023-05-26 | 比音勒芬服饰股份有限公司 | High-elasticity breathable three-dimensional knitwear fabric and preparation method thereof |
Non-Patent Citations (1)
| Title |
|---|
| 铁子涵;王相承;李丹;段圣亮;: "聚酯纤维表面改性的研究及其进展", 化工时刊, no. 08, 26 August 2015 (2015-08-26) * |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN118326597A (en) * | 2024-04-11 | 2024-07-12 | 潮州市丹辉婚纱礼服有限公司 | A weaving method for skin-friendly and breathable fabric |
| CN119711027A (en) * | 2025-02-28 | 2025-03-28 | 上海幼岚纺织科技有限公司 | Moisture-absorbing antibacterial fabric and preparation method thereof |
| CN119711027B (en) * | 2025-02-28 | 2025-05-16 | 上海幼岚纺织科技有限公司 | Moisture-absorbing antibacterial fabric and preparation method thereof |
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