CN105040241B - A kind of preparation method of antibacterial blended yarn weaved fabric - Google Patents

A kind of preparation method of antibacterial blended yarn weaved fabric Download PDF

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CN105040241B
CN105040241B CN201510518278.2A CN201510518278A CN105040241B CN 105040241 B CN105040241 B CN 105040241B CN 201510518278 A CN201510518278 A CN 201510518278A CN 105040241 B CN105040241 B CN 105040241B
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blended yarn
weaved fabric
yarn weaved
antibacterial
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CN105040241A (en
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赵兵
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Shenzhen Yinger Garments Co Ltd
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SUZHOU ZHENGYECHANG INTELLIGENT TECHNOLOGY Co Ltd
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Abstract

The preparation method that the present invention relates to a kind of antibacterial blended yarn weaved fabric, first by cotton for cotton for the warp thread 50%/30% Caulis et Folium Lini/20% bamboo fibre * weft yarn 100% blended yarn weaved fabric grafting one chloro-s-triazine-beta-schardinger dextrin-formed that interweaves, then the blended yarn weaved fabric after one chloro-s-triazine-grafted by beta cyclodextrin is put into the silver nitrate solution dipping 60min of 0.01-10g/L, two leachings two are rolled, and put into heating 8min in the microwave oven of 600W and can obtain antibacterial blended yarn weaved fabric。The present invention, with cotton/Caulis et Folium Lini/bamboo fiber blended fabric for base material, utilizes the one chloro-s-triazine-grafted by beta cyclodextrin method in-situ preparation nanometer silver antimicrobial blended yarn weaved fabric by microwave radiation, and the antibacterial blended yarn weaved fabric prepared has the antibacterial and washing fastness of excellence。

Description

一种抗菌混纺面料的制备方法A kind of preparation method of antibacterial blended fabric

技术领域 technical field

本发明属于纺织领域,特别涉及一种抗菌混纺面料的制备方法。 The invention belongs to the field of textiles, in particular to a method for preparing an antibacterial blended fabric.

背景技术 Background technique

天然纤维素虽然具有穿着舒适性、可再生性和生物可降解性等优点,但在服用过程中,因纤维具有较大的比表面积和较强的吸湿能力,纤维制品极易附着微生物,并为其繁殖和传播创造条件,从而造成纤维强力的损伤、产生污点和褪色、产生令人不愉快的气味,甚至造成疾病的传播,影响人体的健康。因此在纤维素的改性研究中,一个重要的研究方向就是实现纤维素的抗菌性能,减少细菌对人体的侵害。而纳米银由于其安全、无毒、高效的抗菌性能,常被用作抗菌整理剂,并且其抗菌性能持久稳定,适应性强,不易产生抗药性,已在无机抗菌整理剂的应用中占主导地位。 Although natural cellulose has the advantages of wearing comfort, renewability and biodegradability, but in the process of taking, because the fiber has a large specific surface area and strong moisture absorption capacity, fiber products are very easy to attach microorganisms, and for Its reproduction and propagation create conditions that cause damage to fiber strength, stains and discoloration, unpleasant odors, and even the spread of diseases, affecting human health. Therefore, in the research on the modification of cellulose, an important research direction is to realize the antibacterial properties of cellulose and reduce the damage of bacteria to the human body. Nano-silver is often used as an antibacterial finishing agent due to its safe, non-toxic and efficient antibacterial properties, and its long-lasting and stable antibacterial properties, strong adaptability, and not easy to produce drug resistance have dominated the application of inorganic antibacterial finishing agents. status.

纳米银抗菌纺织品的制备方法主要有纤维改性法和织物后整理法。纤维改性法即首先在成纤高聚物中添加纳米银,然后进行湿法或熔融纺丝,再加工制成抗菌织物;织物后整理则是通过在织物表面涂层或浸渍等方式,使纺织材料表面形成纳米银抗菌层。由于棉、丝等天然纤维质地柔软,对人体皮肤具有很好的亲和力,以及良好的吸湿透气,可再生等特性,受到人们的广泛青睐,在人们的日常用生活纺织品中占据绝对地位。而对这种天然纤维的改性只能通过后整理法赋予其抗菌性能。目前,利用后整理法制备抗菌织物的方法很多,如浸渍吸附、多层沉积、溶胶-凝胶涂覆、聚合物混合涂层、超临界二氧化碳等。在这些方法中简单的物理吸附往往牢度不够,使用交联剂固着或聚合物涂层来增加其牢度又会造成织物原有的优异手感、对人体肌肤的亲和力等丧失,并且这些化学试剂的使用不仅会污染环境,整理到织物上还会对人体产生潜在的危害。 The preparation methods of nano-silver antibacterial textiles mainly include fiber modification and fabric finishing. The fiber modification method is to first add nano-silver to the fiber-forming polymer, then perform wet or melt spinning, and then process it into an antibacterial fabric; fabric finishing is to coat or impregnate the surface of the fabric to make it A nano-silver antibacterial layer is formed on the surface of the textile material. Natural fibers such as cotton and silk are soft in texture, have good affinity to human skin, and have good moisture absorption, breathability, and regeneration properties. They are widely favored by people and occupy an absolute position in people's daily life textiles. And the modification of this natural fiber can only endow it with antibacterial properties by finishing method. At present, there are many methods for preparing antibacterial fabrics by post-finishing, such as impregnation adsorption, multi-layer deposition, sol-gel coating, polymer hybrid coating, supercritical carbon dioxide, etc. In these methods, simple physical adsorption is often not fast enough, and the use of cross-linking agents or polymer coatings to increase its fastness will cause the loss of the original excellent hand feel of the fabric, affinity to human skin, etc., and these chemical reagents The use of non-woven fabrics will not only pollute the environment, but also cause potential harm to the human body when it is finished on the fabric.

而原位生成技术能够同时在纤维的表面和内部生成纳米材料,在纤维上分布均匀。并且纳米材料的制备和对纺织材料的整理同时进行,避免了纳米材料在整理过程中团聚的问题。而且原位生成技术使得纳米材料与纤维天然结合牢度高。因此,原位生成纳米银抗菌整理技术以其高效、简便、环保等特性越来越受到广大研究人员的重视。 The in-situ generation technology can simultaneously generate nanomaterials on the surface and inside of the fiber, and distribute them evenly on the fiber. Moreover, the preparation of the nanometer material and the finishing of the textile material are carried out simultaneously, thereby avoiding the problem of agglomeration of the nanometer material during the finishing process. Moreover, the in-situ generation technology makes the natural combination of nanomaterials and fibers high. Therefore, the in-situ generation of nano-silver antibacterial finishing technology has attracted more and more attention from researchers because of its high efficiency, simplicity, and environmental protection.

环糊精是由淀粉通过环糊精葡萄糖基转移酶降解而生成的含有6、7、8个甚至更多葡萄糖单元,彼此间通过α-1,4糖苷键连接而成的环状低聚糖。常见的环糊精有三种:α环糊精(α-CD)、β-环糊精(β-CD)和γ环糊精(γ-CD),它们分别是由6、7、8个葡萄糖单体在C-1和C-4上连接而成的环状低聚糖。而一氯三嗪-β-环糊精(MCT-β-CD)是一种带有特殊活性基团的环糊精衍生物,无毒并且对皮肤不过敏。其分子结构内的一氯三嗪活性基团对亲核基团(如羟基氧负离子、氨基等)具有很强的反应性,二者反应生成共价键后,环糊精母体就能够永久地固定在织物纤维上。 Cyclodextrin is a cyclic oligosaccharide that contains 6, 7, 8 or more glucose units, which are formed by the degradation of starch by cyclodextrin glucosyltransferase, and are connected to each other by α-1,4 glycosidic bonds. . There are three common cyclodextrins: α-cyclodextrin (α-CD), β-cyclodextrin (β-CD) and γ-cyclodextrin (γ-CD), which are composed of 6, 7, and 8 glucose A cyclic oligosaccharide formed by linking monomers at C-1 and C-4. And monochlorotriazine-β-cyclodextrin (MCT-β-CD) is a cyclodextrin derivative with a special active group, non-toxic and non-allergic to the skin. The chlorotriazine active group in its molecular structure has strong reactivity to nucleophilic groups (such as hydroxyl oxyanions, amino groups, etc.), and after the two react to form a covalent bond, the cyclodextrin parent can be permanently Fixes to fabric fibers.

中国发明专利201010166358.3将质量百分比为0.1%~10%的烷基化环糊精水溶液与质量摩尔浓度为0.01~1.0mol/L的银氨溶液以1∶100~1∶10的体积比进行混合,在10~100℃的温度条件下搅拌1~120min,即获得平均粒径为1~100nm的纳米银胶体溶液。刘姣姣等(纺织导报,2013,03:74-76,环糊精/纳米银整理棉织物的研究[D].苏州大学,2013)利用环糊精水解物的还原性还原银氨络离子得到纳米银溶液,并采用纳米银胶体溶液对纯棉织物进行抗菌整理,测试了整理后棉织物的抑菌性能。但是这些文献皆采用直接浸渍吸附法处理棉纤维,但是无机纳米材料由于缺乏与织物的价键作用而牢度较低。 Chinese invention patent 201010166358.3 mixes an aqueous solution of alkylated cyclodextrin with a mass percentage of 0.1% to 10% and a silver ammonia solution with a mass molar concentration of 0.01 to 1.0mol/L at a volume ratio of 1:100 to 1:10, Stirring for 1-120 min under the temperature condition of 10-100 DEG C, namely obtaining nano-silver colloid solution with an average particle diameter of 1-100 nm. Liu Jiaojiao et al. (Textile Herald, 2013, 03:74-76, Research on Cotton Fabric Finishing with Cyclodextrin/Nano-Silver [D]. Soochow University, 2013) obtained nano Silver solution, and using nano-silver colloid solution to antibacterial finishing of pure cotton fabric, tested the antibacterial performance of cotton fabric after finishing. However, these documents all adopt the direct impregnation and adsorption method to process cotton fibers, but the fastness of inorganic nanomaterials is low due to the lack of valence bonds with fabrics.

发明内容 Contents of the invention

本发明针对现有技术存在的不足,旨在提供一种抗菌混纺面料的制备方法。 The invention aims at providing a method for preparing antibacterial blended fabrics aiming at the deficiencies in the prior art.

本发明通过下述技术方案予以实现: The present invention is achieved through the following technical solutions:

所述混纺面料由经纬纱交织形成,所述经纱为50%棉/30%亚麻/20%lyocelllyocell竹纤维,所述纬纱为100%棉,所述经纬纱的线密度为18.2*18.2tex,组织结构3/1斜纹,幅宽60cm,紧度77.04%,厚度0.5mm,织物密度344*264/(根·(10cm)-1)。将上述混纺面料置于1-100g/L的一氯均三嗪-β-环糊精溶液中浸渍1h,浴比1:50,用碳酸钠将溶液的pH调至10-11,二浸二轧,带液率95%,80℃预烘3min,120℃焙烘5min,然后60℃水洗15min。将一氯均三嗪-β-环糊精接枝后的混纺面料放入0.01-10g/L的硝酸银溶液浸渍60min,浴比1:50,二浸二轧,压力为1kg/m2,带液率为90%,在温度为95℃的鼓风烘箱中预烘8min,停滞1min,再在温度为95℃的鼓风烘箱中预烘10min,然后170℃下焙烘5min,从溶液中取出后,放入600W的微波炉中加热8min。 The blended fabric is formed by interweaving warp and weft yarns, the warp yarns are 50% cotton/30% linen/20% lyocelllyocell bamboo fiber, the weft yarns are 100% cotton, and the linear density of the warp and weft yarns is 18.2*18.2tex, the tissue Structure 3/1 twill, width 60cm, tightness 77.04%, thickness 0.5mm, fabric density 344*264/(root·(10cm) -1 ). Put the above blended fabric in 1-100g/L monochloro-s-triazine-β-cyclodextrin solution and soak for 1h, the bath ratio is 1:50, adjust the pH of the solution to 10-11 with sodium carbonate, and dip twice Rolling, with a liquid rate of 95%, pre-baking at 80°C for 3 minutes, baking at 120°C for 5 minutes, and then washing at 60°C for 15 minutes. Immerse the blended fabric grafted with monochloro-s-triazine-β-cyclodextrin in 0.01-10g/L silver nitrate solution for 60min, the bath ratio is 1:50, two dipping and two rolling, the pressure is 1kg/m 2 , The liquid-carrying rate is 90%, pre-baked in a blast oven at 95°C for 8 minutes, stagnant for 1 minute, then pre-baked in a blast oven at 95°C for 10 minutes, and then baked at 170°C for 5 minutes, from the solution After taking it out, heat it in a 600W microwave oven for 8 minutes.

本发明具有如下有益效果: The present invention has following beneficial effect:

本发明以棉/亚麻/竹纤维混纺面料为基材,利用一氯均三嗪-β-环糊精接枝通过微波辐射的方法原位生成纳米银抗菌混纺面料。 The invention uses the cotton/flax/bamboo fiber blended fabric as the base material, utilizes monochloro-s-triazine-β-cyclodextrin to graft and microwave radiation to generate nano-silver antibacterial blended fabric in situ.

(1)微波原位生成整理能够更多的在织物或纤维内部生成,有利于提高其耐洗性。 (1) Microwave in-situ generated finishing can be more generated inside the fabric or fiber, which is beneficial to improve its washability.

(2)微波原位生成整理是将初始液吸收到织物中后再整理,整理后织物即干燥,无任何残留物质,并且初始液可以继续使用,有利于节约成本。 (2) Microwave in-situ finishing is to absorb the initial liquid into the fabric before finishing. After finishing, the fabric is dried without any residual substances, and the initial liquid can be used continuously, which is beneficial to cost saving.

(3)微波原位生成整理加热反应快,效率高,而且安全、方便。 (3) Microwave in-situ generation, finishing and heating have fast response, high efficiency, safety and convenience.

(4)纤维素与一氯均三嗪-β-环糊精发生交联反应,生成一氯均三嗪-β-环糊精接枝纤维素,相对于传统的浸渍处理,一氯均三嗪-β-环糊精与纤维素两者之间的结合牢度大大提高。 (4) The cross-linking reaction between cellulose and monochlorotriazine-β-cyclodextrin produces monochlorotriazine-β-cyclodextrin grafted cellulose. The binding fastness between oxazine-β-cyclodextrin and cellulose is greatly improved.

(5)纳米银的制备和对纤维素的整理可同时进行,避免了纳米银在整理过程中团聚的问题。 (5) The preparation of nano-silver and the finishing of cellulose can be carried out at the same time, which avoids the problem of agglomeration of nano-silver in the finishing process.

具体实施方式 detailed description

下面结合具体实施方式,进一步阐述本发明。 The present invention will be further described below in combination with specific embodiments.

实施例1: Example 1:

混纺面料由经纬纱交织形成,所述经纱为50%棉/30%亚麻/20%lyocell竹纤维,所述纬纱为100%棉,所述经纬纱的线密度为18.2*18.2tex,组织结构3/1斜纹,幅宽60cm,紧度77.04%,厚度0.5mm,织物密度344*264/(根·(10cm)-1)。 The blended fabric is formed by interweaving warp and weft yarns, the warp yarns are 50% cotton/30% linen/20% lyocell bamboo fiber, the weft yarns are 100% cotton, the linear density of the warp and weft yarns is 18.2*18.2tex, and the structure is 3 /1 twill, width 60cm, tightness 77.04%, thickness 0.5mm, fabric density 344*264/(root·(10cm) -1 ).

将上述混纺面料置于10g/L的一氯均三嗪-β-环糊精溶液中浸渍1h,浴比1:50,用碳酸钠将溶液的pH调至10,二浸二轧,带液率95%,80℃预烘3min,120℃焙烘5min,然后60℃水洗15min。将一氯均三嗪-β-环糊精接枝后的混纺面料放入0.1g/L的硝酸银溶液浸渍60min,浴比1:50,二浸二轧,压力为1kg/m2,带液率为90%,在温度为95℃的鼓风烘箱中预烘8min,停滞1min,再在温度为95℃的鼓风烘箱中预烘10min,然后170℃下焙烘5min,从溶液中取出后,放入600W的微波炉中加热8min。 Put the above blended fabric in 10g/L monochloro-s-triazine-β-cyclodextrin solution and immerse it for 1h, the bath ratio is 1:50, adjust the pH of the solution to 10 with sodium carbonate, dipping and rolling twice, with liquid The rate is 95%, pre-baked at 80°C for 3 minutes, baked at 120°C for 5 minutes, and then washed with water at 60°C for 15 minutes. Immerse the blended fabric grafted with monochloro-s-triazine-β-cyclodextrin in 0.1g/L silver nitrate solution for 60 minutes, bath ratio 1:50, two dipping and two rolling, the pressure is 1kg/m 2 , with The liquid rate is 90%, pre-baked in a blast oven at 95°C for 8 minutes, stagnated for 1 minute, then pre-baked in a blast oven at 95°C for 10 minutes, then baked at 170°C for 5 minutes, and removed from the solution Finally, put it into a 600W microwave oven and heat it for 8min.

实施例2: Example 2:

混纺面料由经纬纱交织形成,所述经纱为50%棉/30%亚麻/20%lyocell竹纤维,所述纬纱为100%棉,所述经纬纱的线密度为18.2*18.2tex,组织结构3/1斜纹,幅宽60cm,紧度77.04%,厚度0.5mm,织物密度344*264/(根·(10cm)-1)。 The blended fabric is formed by interweaving warp and weft yarns, the warp yarns are 50% cotton/30% linen/20% lyocell bamboo fiber, the weft yarns are 100% cotton, the linear density of the warp and weft yarns is 18.2*18.2tex, and the structure is 3 /1 twill, width 60cm, tightness 77.04%, thickness 0.5mm, fabric density 344*264/(root·(10cm) -1 ).

将上述混纺面料置于50g/L的一氯均三嗪-β-环糊精溶液中浸渍1h,浴比1:50,用碳酸钠将溶液的pH调至11,二浸二轧,带液率95%,80℃预烘3min,120℃焙烘5min,然后60℃水洗15min。将一氯均三嗪-β-环糊精接枝后的混纺面料放入5g/L的硝酸银溶液浸渍60min,浴比1:50,二浸二轧,压力为1kg/m2,带液率为90%,在温度为95℃的鼓风烘箱中预烘8min,停滞1min,再在温度为95℃的鼓风烘箱中预烘10min,然后170℃下焙烘5min,从溶液中取出后,放入600W的微波炉中加热8min。 Put the above blended fabric in 50g/L monochloro-s-triazine-β-cyclodextrin solution and immerse it for 1h, the bath ratio is 1:50, adjust the pH of the solution to 11 with sodium carbonate, double dipping and rolling, with liquid The rate is 95%, pre-baked at 80°C for 3 minutes, baked at 120°C for 5 minutes, and then washed with water at 60°C for 15 minutes. Immerse the blended fabric grafted with monochloro-s-triazine-β-cyclodextrin in 5g/L silver nitrate solution for 60min, bath ratio 1:50, double dipping and rolling, pressure 1kg/m 2 , with liquid The rate is 90%, pre-baked in a blast oven at 95°C for 8 minutes, stagnant for 1 minute, then pre-baked in a blast oven at 95°C for 10 minutes, and then baked at 170°C for 5 minutes, after taking it out of the solution , Put it into a 600W microwave oven and heat for 8min.

实施例3: Example 3:

混纺面料由经纬纱交织形成,所述经纱为50%棉/30%亚麻/20%lyocell竹纤维,所述纬纱为100%棉,所述经纬纱的线密度为18.2*18.2tex,组织结构3/1斜纹,幅宽60cm,紧度77.04%,厚度0.5mm,织物密度344*264/(根·(10cm)-1)。 The blended fabric is formed by interweaving warp and weft yarns, the warp yarns are 50% cotton/30% linen/20% lyocell bamboo fiber, the weft yarns are 100% cotton, the linear density of the warp and weft yarns is 18.2*18.2tex, and the structure is 3 /1 twill, width 60cm, tightness 77.04%, thickness 0.5mm, fabric density 344*264/(root·(10cm) -1 ).

将上述混纺面料置于100g/L的一氯均三嗪-β-环糊精溶液中浸渍1h,浴比1:50,用碳酸钠将溶液的pH调至11,二浸二轧,带液率95%,80℃预烘3min,120℃焙烘5min,然后60℃水洗15min。将一氯均三嗪-β-环糊精接枝后的混纺面料放入10g/L的硝酸银溶液浸渍60min,浴比1:50,二浸二轧,压力为1kg/m2,带液率为90%,在温度为95℃的鼓风烘箱中预烘8min,停滞1min,再在温度为95℃的鼓风烘箱中预烘10min,然后170℃下焙烘5min,从溶液中取出后,放入600W的微波炉中加热8min。 Put the above blended fabric in 100g/L monochloro-s-triazine-β-cyclodextrin solution and soak for 1h, the bath ratio is 1:50, adjust the pH of the solution to 11 with sodium carbonate, double dipping and rolling, with liquid The rate is 95%, pre-baked at 80°C for 3 minutes, baked at 120°C for 5 minutes, and then washed with water at 60°C for 15 minutes. Immerse the blended fabric grafted with monochloro-s-triazine-β-cyclodextrin in 10g/L silver nitrate solution for 60 minutes, bath ratio 1:50, double dipping and rolling, pressure 1kg/m 2 , with liquid The rate is 90%, pre-baked in a blast oven at 95°C for 8 minutes, stagnant for 1 minute, then pre-baked in a blast oven at 95°C for 10 minutes, and then baked at 170°C for 5 minutes, after taking it out of the solution , Put it into a 600W microwave oven and heat for 8min.

显然,本发明的上述实施例仅仅是为清楚地说明本发明所作的举例,而并非是对本发明的实施方式的限定。对于所属领域的普通技术人员来说,在上述说明的基础上还可以做出其它不同形式的变化或变动。这里无法对所有的实施方式予以穷举。凡是属于本发明的技术方案所引申出的显而易见的变化或变动仍处于本发明的保护范围之列。 Apparently, the above-mentioned embodiments of the present invention are only examples for clearly illustrating the present invention, rather than limiting the implementation of the present invention. For those of ordinary skill in the art, on the basis of the above description, other changes or changes in different forms can also be made. All the implementation manners cannot be exhaustively listed here. All obvious changes or changes derived from the technical solutions of the present invention are still within the protection scope of the present invention.

Claims (5)

1. the preparation method of an antibacterial blended yarn weaved fabric, it is characterised in that:
(1) described blended yarn weaved fabric is formed by warp and weft interweaving, described warp thread is 50% cotton/30% Caulis et Folium Lini/20% bamboo fibre, described weft yarn is 100% cotton, the described line density through weft yarn is 18.2*18.2tex, organizational structure 3/1 twill, fabric width 60cm, tightness 77.04%, in thickness 0.5mm, 10cm width, the radical of warp thread is 344, and the radical of weft yarn is 264;
(2) being placed in by above-mentioned blended yarn weaved fabric in the beta-schardinger dextrin-solution of 1-100g/L and impregnate 1h, bath raio 1:50, with sodium carbonate, the pH of solution is adjusted to 10-11, two leachings two are rolled, liquid carrying rate 95%, 80 DEG C of preliminary drying 3min, and 120 DEG C bake 5min, then 60 DEG C of washing 15min;
(3) being put into by the blended yarn weaved fabric after grafted by beta cyclodextrin certain density silver nitrate solution dipping certain time, bath raio 1:50, two leachings two are rolled, and pressure is 1kg/m2, liquid carrying rate is 90%, preliminary drying 8min in the convection oven that temperature is 95 DEG C, stagnates 1min, then in the convection oven that temperature is 95 DEG C preliminary drying 10min, then bake 5min at 170 DEG C, after taking out from solution, put into heating 8min in the microwave oven of 600W。
2. the preparation method of a kind of antibacterial blended yarn weaved fabric according to claim 1, it is characterised in that described bamboo fibre is lyocell bamboo fibre。
3. the preparation method of a kind of antibacterial blended yarn weaved fabric according to claim 1, it is characterised in that described-beta-schardinger dextrin-is one chloro-s-triazine-beta-schardinger dextrin-。
4. the preparation method of a kind of antibacterial blended yarn weaved fabric according to claim 1, it is characterised in that the concentration of step (3) described silver nitrate solution is 0.01-10g/L。
5. the preparation method of a kind of antibacterial blended yarn weaved fabric according to claim 1, it is characterised in that step (3) described dip time is 60min。
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