CN115387117A - 一种光响应抗菌型织物柔软剂 - Google Patents
一种光响应抗菌型织物柔软剂 Download PDFInfo
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Abstract
本发明涉及织物整理技术领域,公开了一种光响应抗菌型织物柔软剂,包括整理剂A和整理剂B,整理剂A天然抗菌剂5.0‑20.0g/L、光响应抗菌剂1.0‑10.0g/L、戊二醛1.5‑10.0g/L、柠檬酸1.5‑10.0g/L、柔软剂10.0‑15.0g/L和渗透剂2.0‑4.5g/L,整理剂B包括1.0‑2.5g/L阿拉伯胶;整理剂A使用后将整理剂B混入整理剂A中。本发明中的光响应抗菌型织物柔软剂安全、环保,经本发明的光响应抗菌型织物柔软剂整理后的织物,洗涤50次以后仍能保持良好的抗菌性,解决了织物抗菌性不能长久有效的问题。并且,经本发明中的抗菌型柔软剂整理后的织物,手感柔软,使用舒适。
Description
技术领域
本发明涉及织物整理技术领域,具体涉及一种光响应抗菌型织物柔软剂。
背景技术
随着人们对织物的要求越来越高,纺织行业通过对织物的各种后整理,使得织物具有各种更优的性能,以应对逐步更迭的市场。其中,织物的柔软整理是一个非常重要的处理工艺,柔软整理会使得织物具有优良的柔软性,以便在使用时为人们提供良好的舒适感。除了柔软性外,人们也越来越重视织物的抗菌性。目前,已经存在向织物的柔软整理液中添加抗菌剂的做法,从而使得整理后的织物具有优良的柔软性的同时,还具有良好的抗菌性。其中,添加的抗菌剂可分为无机抗菌剂、有机抗菌剂和天然抗菌剂等。其中,虽然无机抗菌剂例如金属银抗菌剂对人体无害,但存在不耐氯、不耐光或热的缺点,而有机抗菌剂存在生物安全性的问题,应用在织物中存在较大难度。而天然抗菌剂安全、环保,是作为织物抗菌整理的首选。但是,虽然织物在使用天然抗菌剂进行抗菌整理后具有良好的抗菌性,但织物的耐洗性较差,织物在洗涤20~50次后,其抗菌性下降了50%甚至更多。也就是说,目前,使用天然抗菌剂进行抗菌整理后得到的织物,存在抗菌性难以长久有效的问题。
发明内容
鉴于以上所述现有技术的缺点,本发明的目的在于提供一种光响应抗菌型织物柔软剂,用于解决现有技术中使用天然抗菌剂进行抗菌整理后,织物的抗菌性不能长久的问题。
为实现上述目的及其他相关目的,本发明提供一种光响应抗菌型织物柔软剂,包括整理剂A和整理剂B,所述整理剂A包括天然抗菌剂5.0-20.0g/L、光响应抗菌剂1.0-10.0g/L、戊二醛1.5-10.0g/L、柠檬酸1.5-10.0g/L、柔软剂10.0-15.0g/L和渗透剂2.0-4.5g/L,所述整理剂B包括1.0-2.5g/L阿拉伯胶;整理剂A使用后将整理剂B混入整理剂A中。
可选地,所述天然抗菌剂包括壳聚糖、芦荟汁、桧油、鱼腥草提取物和大黄提取物中的一种或两种以上。
可选地,所述光响应抗菌剂包括纳米二氧化钛和掺杂有银和镍的二氧化钛复合抗菌粉体中的一种或两种。
可选地,所述天然抗菌剂包括壳聚糖和/或芦荟汁,天然抗菌剂还包括桧油、鱼腥草提取物和大黄提取物中的一种或两种以上。
可选地,所述鱼腥草提取物为鱼腥草切段后与50-60%乙醇溶液在料液比1:10-15、温度50-55℃条件下回流得到的提取液浓缩得到。
可选地,所述大黄提取物的制备方法如下:将大黄片或大黄粉与50-60%乙醇溶液在料液比1:4-8条件下浸泡24h以上,过滤得滤液,向滤液中加入浓度为36-38%的盐酸溶液,静置30min以上后浓缩得到;其中,滤液与盐酸溶液的体积比为1:15-20。
可选地,所述整理剂A还包括乳化剂。
可选地,所述整理剂A还包括季戊四醇。
可选地,所述乳化剂为失水山梨醇脂肪酸酯和蔗糖脂肪酸酯中的一种或两种。
可选地,所述乳化剂在整理剂A中的浓度为4.0-8.0g/L,所述季戊四醇在整理剂A中的浓度为1.0-10.0g/L。
本发明还提供一种上述光响应抗菌型织物柔软剂的制备方法,包括以下步骤:
S1:将天然抗菌剂、光响应抗菌剂、戊二醛、柠檬酸、乳化剂、季戊四醇和水混合,得到第一混合液;
S2:将柔软剂和渗透剂添加至第一混合液中,混合后得到整理剂A;
S3:将阿拉伯胶和水混合,得到整理剂B。
本发明还提供一种上述光响应抗菌型织物柔软剂用于整理织物的整理方法,包括以下步骤:
1)将织物浸泡于35-45℃的整理剂A中,20-25min后取出织物,加入整理剂B并搅拌混合得到混合整理剂,将织物浸泡于混合整理剂中,10-15min后进行浸轧处理,轧余率为60-80%;
2)浸轧后30-45℃烘至7-8成干,得到7-8成干织物;
3)将7-8成干织物进行焙烘处理,焙烘温度为110-130℃,焙烘时长为3-5min,得到整理后的织物。
如上所述,本发明的光响应抗菌型织物柔软剂,具有以下有益效果:
1、本发明中的光响应抗菌型织物柔软剂,包括整理剂A和整理剂B,且先使用整理剂A后使用整理剂B,先利用整理剂A在织物表面交联上天然抗菌剂,再利用整理剂B在织物表面形成膜,进一步加强天然抗菌剂在织物表面的固着力。并且,本方案中,整理剂A中的光响应抗菌剂附着在织物内,整理剂B还能够加强光响应催化剂在织物上的附着力,延长天然抗菌剂和光响应抗菌剂在织物上的停留时间,从而延长织物的抗菌时效。因此,本发明不仅能够使得织物具有优良的柔软性和良好的抗菌性,还能够使得织物在洗涤50次后,仍能保持70%上的抑菌率,即织物的耐洗性好,织物的抗菌性能长久保持。
2、本发明中的光响应抗菌型织物柔软剂安全、环保,且用于整理织物的整理方法简单,易于工业化生产。
具体实施方式
以下通过特定的具体实例说明本发明的实施方式,本领域技术人员可由本说明书所揭露的内容轻易地了解本发明的其他优点与功效。本发明还可以通过另外不同的具体实施方式加以实施或应用,本说明书中的各项细节也可以基于不同观点与应用,在没有背离本发明的精神下进行各种修饰或改变。
本发明提供一种光响应抗菌型织物柔软剂,包括整理剂A和整理剂B,整理剂A包括天然抗菌剂5.0-20.0g/L、光响应抗菌剂1.0-10.0g/L、戊二醛1.5-10.0g/L、柠檬酸1.5-10.0g/L、柔软剂10.0-15.0g/L和渗透剂2.0-4.5g/L,整理剂B包括1.0-2.5g/L阿拉伯胶;整理剂A使用后将整理剂B混入整理剂A中。
在整理剂A中的天然抗菌剂包括壳聚糖、芦荟汁、桧油、鱼腥草提取物和大黄提取物中的一种或两种以上。其中,芦荟汁为新鲜芦荟清洗后榨汁得到。鱼腥草提取物为鱼腥草切段后与50-60%乙醇溶液在料液比1:10-15、温度50-55℃条件下回流得到的提取液浓缩得到。大黄提取物的制备方法如下:将大黄片或大黄粉与50-60%乙醇溶液在料液比1:4-8条件下浸泡24h以上,过滤得滤液,向滤液中加入浓度为36-38%的盐酸溶液,静置30min以上后浓缩得到;其中,滤液与盐酸溶液的体积比为1:15-20。
在整理剂A中的光响应抗菌剂包括纳米二氧化钛和掺杂有银和镍的二氧化钛复合抗菌粉体中的一种或两种,其中,纳米二氧化钛为市售产品,而掺杂有银和镍的二氧化钛复合抗菌粉体的制备方法如下:(1)室温下将一定摩尔比的钛酸正丁酯与冰乙酸加入盛有无水乙醇的烧杯中,搅拌0.5h使之混合均匀,得淡黄色透明液a;向适量水与无水乙醇配成的溶液中滴加浓硝酸,调pH=1.0,充分搅拌得均匀液b;剧烈搅拌下将b以12滴/min滴加至a中,得均匀透明液A(此时pH=5.0),搅拌3h。(2)称取适量的硝酸银和硝酸镍,溶解于适量蒸馏水中得液B。(3)取适量液B在搅拌状态下缓慢滴加至适量液A中,静置,陈化一定时间后得湿凝胶,将湿凝胶置于干燥箱中,于100℃干燥8h,得到干凝胶。(4)将干凝胶研磨后置于马弗炉中,于700℃下保温3h,得到最终产物——掺杂了银和镍的二氧化钛复合抗菌粉体。
在本发明的另一实施例中,整理剂A还包括乳化剂,乳化剂为失水山梨醇脂肪酸酯和蔗糖脂肪酸酯中的一种或两种,乳化剂整理剂A中的浓度为4.0-8.0g/L。失水山梨醇脂肪酸酯和蔗糖脂肪酸酯中均含有较多的羟基,可使柔软剂达到更好的乳化效果,提高整个体系的分散性和均匀性。
在本发明的另一实施例中,整理剂A还包括季戊四醇,季戊四醇在整理剂A中的浓度为1.0-10.0g/L。季戊四醇含有四个化学环境相同的羟基,整体呈正四边形结构,能够与天然抗菌剂形成多方位的氢键,提高天然抗菌剂之间的结合力,使得天然抗菌剂在织物表面形成交联之后的结构更加稳定,提高天然抗菌剂在织物表面的固着力,使得织物具有更长效的抗菌性。
本发明还提供一种上述光响应抗菌型织物柔软剂的制备方法,包括以下步骤:
S1:将天然抗菌剂、光响应抗菌剂、戊二醛、柠檬酸、乳化剂、季戊四醇和水混合,在75-85℃条件下搅拌30-35min,得到第一混合液;
S2:将柔软剂和渗透剂添加至第一混合液中,在45-50℃条件下搅拌35-40min,得到整理剂A;
S3:将阿拉伯胶和水混合,在30-35℃条件下搅拌20-25min,得到整理剂B。
本发明还提供一种上述光响应抗菌型织物柔软剂用于整理织物的整理方法,包括以下步骤:
1)将织物浸泡于35-45℃的整理剂A中,浸泡过程中织物每分钟翻面20-30次,浸泡20-25min后取出织物,加入整理剂B并搅拌混合得到混合整理剂,将织物浸泡于混合整理剂中,10-15min后进行浸轧处理,轧余率为60-80%;
2)浸轧后30-45℃烘至7-8成干,得到7-8成干织物;
3)将7-8成干织物进行焙烘处理,焙烘温度为110-130℃,焙烘时长为3-5min,得到整理后的织物。
下面通过具体的例举实施例以详细说明本发明。同样应理解,以下实施例只用于对本发明进行具体的说明,不能理解为对本发明保护范围的限制,本领域的技术人员根据本发明的上述内容作出的一些非本质的改进和调整均属于本发明的保护范围。下述示例具体的工艺参数等也仅是合适范围中的一个示例,即本领域技术人员可以通过本文的说明做合适的范围内选择,而并非要限定于下文示例的具体数值。
实施例1
一种光响应抗菌型织物柔软剂,包括整理剂A和整理剂B,整理剂A包括天然抗菌剂5.0g/L、光响应抗菌剂1.0g/L、戊二醛1.5g/L、柠檬酸3.0g/L、柔软剂10.0g/L、渗透剂4.5g/L和乳化剂4.0g/L,整理剂B包括1.0g/L阿拉伯胶;整理剂A使用后将整理剂B混入整理剂A中。
天然抗菌剂为壳聚糖、桧油和鱼腥草提取物,壳聚糖、桧油和鱼腥草提取物之间的质量比可以为任意比,本实施例中,壳聚糖、桧油和鱼腥草提取物之间的质量比为1:0.5:0.5。鱼腥草提取物的制备方法如下:鱼腥草切段后与50%乙醇溶液在料液比1:15、温度50-55℃条件下回流3次,每次2h,合并得到的提取液,将提取液浓缩至相对密度为1.20-1.25,得到鱼腥草提取物。
整理剂A中的光响应抗菌剂为掺杂有银和镍的二氧化钛复合抗菌粉体。
整理剂A中的柔软剂为有机硅柔软剂,本实施例中有机硅柔软剂具体为氨基硅油和羟基封端聚甲基硅油,氨基硅油和羟基封端聚甲基硅油的质量比为1:1。
整理剂A中的渗透剂为渗透剂JFC。
整理剂A中的乳化剂为失水山梨醇脂肪酸酯和蔗糖脂肪酸酯,失水山梨醇脂肪酸酯和蔗糖脂肪酸酯的质量比为2:1。
一种光响应抗菌型织物柔软剂的制备方法,包括以下步骤:
S1:将壳聚糖、桧油、鱼腥草提取物、光响应抗菌剂、戊二醛、柠檬酸、失水山梨醇脂肪酸酯、蔗糖脂肪酸酯和水按比例混合,在75℃条件下搅拌35min,得到第一混合液;
S2:将氨基硅油、羟基封端聚甲基硅油和渗透剂JFC按比例添加至第一混合液中,在45℃条件下搅拌40min,降至常温后得到整理剂A;
S3:将阿拉伯胶和水按比例混合,在35℃条件下搅拌20min,得到整理剂B。
一种光响应抗菌型织物柔软剂用于整理织物的整理方法,包括以下步骤:
1)将织物浸泡于35℃的整理剂A中,浸泡过程中织物每分钟翻面20次,浸泡25min后取出织物,向整理剂A中加入整理剂B并搅拌混合得到混合整理剂,将织物浸泡于混合整理剂中,10min后进行浸轧处理,轧余率为60%;
2)浸轧后45℃烘至7-8成干,得到7-8成干织物;
3)将7-8成干织物进行焙烘处理,焙烘温度为130℃,焙烘时长为3min,得到整理后的织物。
实施例2
本实施例与实施例1的不同之处在于:
本实施例中的一种光响应抗菌型织物柔软剂,整理剂A还包括季戊四醇,季戊四醇在整理剂A中的浓度为1.0g/L。其余均与实施例1相同。
本实施例中的一种光响应抗菌型织物柔软剂的制备方法,在步骤S1中,将壳聚糖、桧油、鱼腥草提取物、光响应抗菌剂、戊二醛、柠檬酸、失水山梨醇脂肪酸酯、蔗糖脂肪酸酯、季戊四醇和水按比例混合,在75℃条件下搅拌35min,得到第一混合液。其余步骤均与实施例1相同。
实施例3
本实施例与实施例2的不同之处在于:
本实施例中的一种光响应抗菌型织物柔软剂,整理剂A中的天然抗菌剂为壳聚糖、鱼腥草提取物和大黄提取物,壳聚糖、鱼腥草提取物和大黄提取物之间的质量比可以为任意比,本实施例中,壳聚糖、鱼腥草提取物和大黄提取物之间的质量比为1:0.5:0.5。大黄提取物的制备方法如下:将大黄片或大黄粉与60%乙醇溶液在料液比1:4条件下浸泡24h,过滤得滤液,向滤液中加入浓度为36%的盐酸溶液,静置30min后浓缩至相对密度为1.20-1.25,得到大黄提取物;其中,滤液与盐酸溶液的体积比为1:15。其余均与实施例2相同。
本实施例中的一种光响应抗菌型织物柔软剂的制备方法,在步骤S1中,将壳聚糖、鱼腥草提取物、大黄提取物、光响应抗菌剂、戊二醛、柠檬酸、失水山梨醇脂肪酸酯、蔗糖脂肪酸酯、季戊四醇和水按比例混合,在75℃条件下搅拌35min,得到第一混合液。其余步骤均与实施例2相同。
实施例4
本实施例与实施例2的不同之处在于:
本实施例中的一种光响应抗菌型织物柔软剂,整理剂A中的天然抗菌剂为壳聚糖和芦荟汁,壳聚糖和芦荟汁的质量比可以为任意比,本实施例中,壳聚糖和芦荟汁的质量比为1:1。芦荟汁为新鲜芦荟清洗后榨汁得到。整理剂A中戊二醛浓度为3.0g/L,其余均与实施例2相同。
本实施例中的一种光响应抗菌型织物柔软剂的制备方法,在步骤S1中,将壳聚糖、芦荟汁、光响应抗菌剂、戊二醛、柠檬酸、失水山梨醇脂肪酸酯、蔗糖脂肪酸酯、季戊四醇和水按比例混合,在75℃条件下搅拌35min,得到第一混合液。其余步骤均与实施例2相同。
实施例5
本实施例与实施例2的不同之处在于:
本实施例中的一种光响应抗菌型织物柔软剂,在整理剂A中,天然抗菌剂、光响应抗菌剂、戊二醛、柠檬酸、柔软剂、渗透剂、乳化剂和季戊四醇的浓度分别为:20.0g/L、10.0g/L、10.0g/L、10.0g/L、15.0g/L、4.5g/L、8.0g/L和10.0g/L。
本实施例其余部分均与实施例2相同。
实施例6
本实施例与实施例2的不同之处在于:
本实施例中的一种光响应抗菌型织物柔软剂,在整理剂A中,天然抗菌剂、戊二醛、柠檬酸、柔软剂、渗透剂、乳化剂和季戊四醇的浓度分别为:10.0g/L、5.0g/L、5.0g/L、5.5g/L、12.0g/L、3.5g/L、4.5g/L和5.5g/L。
本实施例其余部分均与实施例2相同。
实施例7
本实施例与实施例5的不同之处在于:
本实施例中的一种光响应抗菌型织物柔软剂,在整理剂B中,阿拉伯胶的浓度为2.5g/L。
本实施例其余部分均与实施例5相同。
对比例1
本对比例与实施例1相比,不同之处在于:本对比例中的柔软剂中不含戊二醛和阿拉伯胶,即本对比例中的柔软剂为天然抗菌剂5.0g/L、光响应抗菌剂1.0g/L、柠檬酸3.0g/L、柔软剂10.0g/L、渗透剂4.5g/L和乳化剂4.0g/L。天然抗菌剂、光响应抗菌剂、柔软剂、渗透剂和乳化剂的选择均与实施例1相同。
使用本对比例中的柔软剂整理织物的整理方法如下:
1)将织物浸泡于35℃的柔软剂中,浸泡过程中织物每分钟翻面20次,浸泡25min后不再翻面,35min后进行浸轧处理,轧余率为60%;
2)浸轧后45℃烘至7-8成干,得到7-8成干织物;
3)将7-8成干织物进行焙烘处理,焙烘温度为130℃,焙烘时长为3min,得到整理后的织物。
对比例2
本对比例与实施例1相比,不同之处在于:本对比例中的柔软剂中不含戊二醛,即本对比例中的柔软剂为天然抗菌剂5.0g/L、光响应抗菌剂1.0g/L、柠檬酸3.0g/L、柔软剂10.0g/L、渗透剂4.5g/L、乳化剂4.0g/L和阿拉伯胶1.0g/L。天然抗菌剂、柔软剂、渗透剂和乳化剂的选择均与实施例1相同。
使用本对比例中的柔软剂整理织物的整理方法如下:
1)将织物浸泡于35℃的柔软剂中,浸泡过程中织物每分钟翻面20次,浸泡25min后不再翻面,35min后进行浸轧处理,轧余率为60%;
2)浸轧后45℃烘至7-8成干,得到7-8成干织物;
3)将7-8成干织物进行焙烘处理,焙烘温度为130℃,焙烘时长为3min,得到整理后的织物。
按照“GB/T 20994.3-2008纺织品抗菌性能的评价第3部分:振荡法”对实施1-7以及对比例1-2中经整理后得到的织物进行抗菌性测试,得到的结果记为初始抑菌率;然后,将织物按照以下方法进行洗涤:在25℃下,使用浓度为20%的硬脂酸钠溶液浸泡织物5min,然后使用清水清洗5遍,烘干,完成一次洗涤。在织物洗涤10次、20次、50次后按照“GB/T20994.3-2008纺织品抗菌性能的评价第3部分:振荡法”对织物进行抗菌性测试,结果如表1所示。
表1各实施例和对比例中织物的抗菌性测试结果
(注:对金黄色葡萄球菌及大肠杆菌的抑菌率≥70%,样品具有抗菌效果)
由表1可知,实施例1中的织物经50次洗涤后,其抑菌率分别为71%和72%,相较于其初始抑菌率,抑菌率分别下降了21.98%和20.00%。而对比例1中的织物经50次洗涤后,其抑菌率相较于其初始抑菌率,分别下降了52.81%和54.55%,对比例2中的织物经50次洗涤后,其抑菌率相较于其初始抑菌率,分别下降了46.67%和48.31%。这说明,本发明中的光响应抗菌型织物柔软剂,整理织物后,不仅能够使得织物具有良好的抗菌性,还能够使得织物在洗涤50次后,其抑菌率仍能保持在70%以上,具有抗菌性,即能够使得织物的抗菌性长久保持。
上述实施例仅例示性说明本发明的原理及其功效,而非用于限制本发明。任何熟悉此技术的人士皆可在不违背本发明的精神及范畴下,对上述实施例进行修饰或改变。因此,举凡所属技术领域中具有通常知识者在未脱离本发明所揭示的精神与技术思想下所完成的一切等效修饰或改变,仍应由本发明的权利要求所涵盖。
Claims (10)
1.一种光响应抗菌型织物柔软剂,其特征在于:包括整理剂A和整理剂B,所述整理剂A包括天然抗菌剂5.0-20.0g/L、光响应抗菌剂1.0-10.0g/L、戊二醛1.5-10.0g/L、柠檬酸1.5-10.0g/L、柔软剂10.0-15.0g/L和渗透剂2.0-4.5g/L,所述整理剂B包括1.0-2.5g/L阿拉伯胶;整理剂A使用后将整理剂B混入整理剂A中。
2.根据权利要求1所述的光响应抗菌型织物柔软剂,其特征在于:所述天然抗菌剂包括壳聚糖、芦荟汁、桧油、鱼腥草提取物和大黄提取物中的一种或两种以上;
和/或,所述光响应抗菌剂包括纳米二氧化钛和掺杂有银和镍的二氧化钛复合抗菌粉体中的一种或两种。
3.根据权利要求2所述的光响应抗菌型织物柔软剂,其特征在于:所述天然抗菌剂包括壳聚糖和/或芦荟汁,天然抗菌剂还包括桧油、鱼腥草提取物和大黄提取物中的一种或两种以上。
4.根据权利要求2所述的光响应抗菌型织物柔软剂,其特征在于:所述鱼腥草提取物为鱼腥草切段后与50-60%乙醇溶液在料液比1:10-15、温度50-55℃条件下回流得到的提取液浓缩得到。
5.根据权利要求2所述的光响应抗菌型织物柔软剂,其特征在于:所述大黄提取物的制备方法如下:将大黄片或大黄粉与50-60%乙醇溶液在料液比1:4-8条件下浸泡24h以上,过滤得滤液,向滤液中加入浓度为36-38%的盐酸溶液,静置30min以上后浓缩得到;其中,滤液与盐酸溶液的体积比为1:15-20。
6.根据权利要求1所述的光响应抗菌型织物柔软剂,其特征在于:所述整理剂A还包括乳化剂;
和/或,所述整理剂A还包括季戊四醇。
7.根据权利要求6所述的光响应抗菌型织物柔软剂,其特征在于:所述乳化剂为失水山梨醇脂肪酸酯和蔗糖脂肪酸酯中的一种或两种。
8.根据权利要求6所述的光响应抗菌型织物柔软剂,其特征在于:所述乳化剂在整理剂A中的浓度为4.0-8.0g/L,所述季戊四醇在整理剂A中的浓度为1.0-10.0g/L。
9.如权利要求6所述的光响应抗菌型织物柔软剂的制备方法,其特征在于:包括以下步骤:
S1:将天然抗菌剂、光响应抗菌剂、戊二醛、柠檬酸、乳化剂、季戊四醇和水混合,得到第一混合液;
S2:将柔软剂和渗透剂添加至第一混合液中,混合后得到整理剂A;
S3:将阿拉伯胶和水混合,得到整理剂B。
10.如权利要求1至8中任一项所述的光响应抗菌型织物柔软剂用于整理织物的整理方法,其特征在于:包括以下步骤:
1)将织物浸泡于35-45℃的整理剂A中,20-25min后取出织物,加入整理剂B并搅拌混合得到混合整理剂,将织物浸泡于混合整理剂中,10-15min后进行浸轧处理,轧余率为60-80%;
2)浸轧后30-45℃烘至7-8成干,得到7-8成干织物;
3)将7-8成干织物进行焙烘处理,焙烘温度为110-130℃,焙烘时长为3-5min,得到整理后的织物。
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