CN113652856A - 一种抗皱棉麻织物的制备方法 - Google Patents
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Abstract
本发明涉及一种抗皱棉麻织物的制备方法,属于纺织加工技术领域。先将棉麻织物加入到氢氧化钠溶液中,浸渍处理25‑35min后,取出,得到处理后的棉麻织物,将其加入到抗皱整理液中,40‑80℃处理50‑70min,取出后70‑90℃预烘5‑7min,再150‑170℃烘焙2‑4min,最后水洗烘干,得到抗皱棉麻织物;所述抗皱整理液中,壳聚糖季铵盐的浓度为6‑10g/L,柠檬酸的浓度为8‑12g/L。本发明先对棉麻织物进行碱处理,改善其柔软性能,再使用壳聚糖季铵盐和柠檬酸的混合溶液对其进行抗皱整理。本发明采用的整理剂成分安全环保,采用本发明方法得到的棉麻织物具有优异的抗皱效果,并且透气性和柔软性佳。
Description
技术领域
本发明涉及一种抗皱棉麻织物的制备方法,属于纺织加工技术领域。
背景技术
棉麻面料是由一半麻和一半棉混合纺织的织物,同时兼具麻和棉的特点。麻织物具有刚性大、耐磨、透气等优点,但存在手感粗糙、弹性较差,容易摩擦起皱等缺点,贴身穿起来对皮肤的摩擦感很明显,时间一长也比较容易起球,而纯棉衣料又有质地太轻的缺点,穿起来软绵绵的,没有麻的坚挺感。而棉麻混合面料有效避免了麻和棉各自的缺点,两者优劣互补,成为现代都市人们对天然、健康、舒适衣物的最佳选择。
然而棉麻织物具有折皱性较大的缺点,其制成的服装成品在搓揉和摩擦中容易起皱,丧失了与人体结合的美学性,影响了衣物的穿着效果,并且容易在折皱处形成磨损,降低了使用性,对棉麻面料的防皱整理是保证棉麻织物优良性能的必要程序。现有的防皱整理剂含有大量的污染性成分,不符合环保要求且影响消费者健康,而且整理后的棉麻织物抗皱效果不佳。因此,有必要开发一种抗皱效果好且绿色环保的防皱整理剂,以满足消费者的需求和健康。
发明内容
本发明的目的在于解决现有技术存在的难题,提供一种抗皱棉麻织物的制备方法,操作简单,采用的整理剂成分安全环保,制得的棉麻织物具有优异的抗皱效果,并且透气性和柔软性佳。
技术方案
一种抗皱棉麻织物的制备方法,包括如下步骤:
(1)将棉麻织物加入到氢氧化钠溶液中,浴比1:50,浸渍处理25-35min后,取出,得到处理后的棉麻织物;
(2)将处理后的棉麻织物加入到抗皱整理液中,浴比1:50,40-80℃处理50-70min,然后取出,70-90℃预烘5-7min,再150-170℃烘焙2-4min,最后水洗烘干,得到抗皱棉麻织物;
步骤(2)中,所述抗皱整理液中,壳聚糖季铵盐的浓度为6-10g/L,柠檬酸的浓度为8-12g/L。
进一步,步骤(1)中,所述氢氧化钠溶液的浓度为12g/L。
进一步,步骤(1)中,所述处理温度为80℃。
进一步,步骤(2)中,所述抗皱整理液中,壳聚糖季铵盐的浓度为8g/L,柠檬酸的浓度为12g/L。
进一步,步骤(2)中,所述处理温度为60℃。
本发明的有益效果:
本发明先对棉麻织物进行碱处理,改善其柔软性能,再使用壳聚糖季铵盐和柠檬酸的混合溶液对其进行抗皱整理,得到抗皱棉麻织物。本发明采用的整理剂成分安全环保,采用本发明方法得到的棉麻织物具有优异的抗皱效果,并且透气性和柔软性佳。
具体实施方式
下面结合具体的实施例对本发明的技术方案做进一步的说明。
实施例1
一种抗皱棉麻织物的制备方法,包括如下步骤:
(1)将棉麻织物加入到12g/L的氢氧化钠溶液中,浴比1:50,80℃浸渍处理30min后,取出,得到处理后的棉麻织物;
(2)将处理后的棉麻织物加入到抗皱整理液中,浴比1:50,40℃处理60min,然后取出,80℃预烘5min,再160℃烘焙3min,最后水洗烘干,得到抗皱棉麻织物;
步骤(2)中,所述抗皱整理液中,壳聚糖季铵盐的浓度为6g/L,柠檬酸的浓度为8g/L。
实施例2
一种抗皱棉麻织物的制备方法,包括如下步骤:
(1)将棉麻织物加入到12g/L的氢氧化钠溶液中,浴比1:50,80℃浸渍处理30min后,取出,得到处理后的棉麻织物;
(2)将处理后的棉麻织物加入到抗皱整理液中,浴比1:50,60℃处理60min,然后取出,80℃预烘5min,再160℃烘焙3min,最后水洗烘干,得到抗皱棉麻织物;
步骤(2)中,所述抗皱整理液中,壳聚糖季铵盐的浓度为6g/L,柠檬酸的浓度为10g/L。
实施例3
一种抗皱棉麻织物的制备方法,包括如下步骤:
(1)将棉麻织物加入到12g/L的氢氧化钠溶液中,浴比1:50,80℃浸渍处理30min后,取出,得到处理后的棉麻织物;
(2)将处理后的棉麻织物加入到抗皱整理液中,浴比1:50,80℃处理60min,然后取出,80℃预烘5min,再160℃烘焙3min,最后水洗烘干,得到抗皱棉麻织物;
步骤(2)中,所述抗皱整理液中,壳聚糖季铵盐的浓度为6g/L,柠檬酸的浓度为12g/L。
实施例4
一种抗皱棉麻织物的制备方法,包括如下步骤:
(1)将棉麻织物加入到12g/L的氢氧化钠溶液中,浴比1:50,80℃浸渍处理30min后,取出,得到处理后的棉麻织物;
(2)将处理后的棉麻织物加入到抗皱整理液中,浴比1:50,60℃处理60min,然后取出,80℃预烘5min,再160℃烘焙3min,最后水洗烘干,得到抗皱棉麻织物;
步骤(2)中,所述抗皱整理液中,壳聚糖季铵盐的浓度为8g/L,柠檬酸的浓度为12g/L。
实施例5
一种抗皱棉麻织物的制备方法,包括如下步骤:
(1)将棉麻织物加入到12g/L的氢氧化钠溶液中,浴比1:50,80℃浸渍处理30min后,取出,得到处理后的棉麻织物;
(2)将处理后的棉麻织物加入到抗皱整理液中,浴比1:50,40℃处理60min,然后取出,80℃预烘5min,再160℃烘焙3min,最后水洗烘干,得到抗皱棉麻织物;
步骤(2)中,所述抗皱整理液中,壳聚糖季铵盐的浓度为8g/L,柠檬酸的浓度为10g/L。
实施例6
一种抗皱棉麻织物的制备方法,包括如下步骤:
(1)将棉麻织物加入到12g/L的氢氧化钠溶液中,浴比1:50,80℃浸渍处理30min后,取出,得到处理后的棉麻织物;
(2)将处理后的棉麻织物加入到抗皱整理液中,浴比1:50,40℃处理60min,然后取出,80℃预烘5min,再160℃烘焙3min,最后水洗烘干,得到抗皱棉麻织物;
步骤(2)中,所述抗皱整理液中,壳聚糖季铵盐的浓度为10g/L,柠檬酸的浓度为10g/L。
实施例7
一种抗皱棉麻织物的制备方法,包括如下步骤:
(1)将棉麻织物加入到12g/L的氢氧化钠溶液中,浴比1:50,80℃浸渍处理30min后,取出,得到处理后的棉麻织物;
(2)将处理后的棉麻织物加入到抗皱整理液中,浴比1:50,80℃处理60min,然后取出,80℃预烘5min,再160℃烘焙3min,最后水洗烘干,得到抗皱棉麻织物;
步骤(2)中,所述抗皱整理液中,壳聚糖季铵盐的浓度为10g/L,柠檬酸的浓度为12g/L。
将实施例1-7制得的抗皱棉麻织物进行抗皱性能、柔软性及透气性能的测试,其中,抗皱性能的测试方法参考的是AATCC 66-2008,使用凸样法(垂直折痕法),压力的负荷为1kg,受压时间为5min,试样回复翼尺寸:长为20mm,宽为15mm,固定翼尺寸:长为40mm,宽为20mm;受压结束15s测得急弹性回复角,再过5min之后测得缓弹性回复角,用缓弹性回复角减去急弹性回复角,并记录数据;柔软性评估的是织物的抗弯刚度,测试方法参考GB/T18318.1-2009中的方法进行,采用YG(B)022型自动织物硬挺度试验仪进行测试,沿着织物的经向和纬向分别剪取25mm×250mm的样品各六个,并标记试样的正反面,按“设定”键,设定单位质量、角度、方法、次数和速度后,旋转仪器上的角度调节按钮,按下“工作”键,等待仪器自动停止并返回初始位置时,记录显示的抗弯刚度数据;透气性能的测试方法按照GB/T5453-1997中的方法进行,采用的是YG461E型数字式透气量仪。测试结果见表1:
表1
由表1的测试结果可以看出,与未经处理的棉麻织物相比,本发明实施例1-7制得的抗皱棉麻织物的抗皱性能和透气性均有大幅度提升,并且抗弯刚度下降,表明织物的柔软性得到提高。
以上所述仅为本发明的优选实施例而已,并不用于限制本发明,对于本领域的技术人员来说,本发明可以有各种更改和变化。凡在本发明的精神和原则之内,所作的任何修改、等同替换、改进等,均应包含在本发明的保护范围之内。
Claims (5)
1.一种抗皱棉麻织物的制备方法,其特征在于,包括如下步骤:
(1)将棉麻织物加入到氢氧化钠溶液中,浴比1:50,浸渍处理25-35min后,取出,得到处理后的棉麻织物;
(2)将处理后的棉麻织物加入到抗皱整理液中,浴比1:50,40-80℃处理50-70min,然后取出,70-90℃预烘5-7min,再150-170℃烘焙2-4min,最后水洗烘干,得到抗皱棉麻织物;
步骤(2)中,所述抗皱整理液中,壳聚糖季铵盐的浓度为6-10g/L,柠檬酸的浓度为8-12g/L。
2.如权利要求1所述抗皱棉麻织物的制备方法,其特征在于,步骤(1)中,所述氢氧化钠溶液的浓度为12g/L。
3.如权利要求1所述抗皱棉麻织物的制备方法,其特征在于,步骤(1)中,所述处理温度为80℃。
4.如权利要求1所述抗皱棉麻织物的制备方法,其特征在于,步骤(2)中,所述抗皱整理液中,壳聚糖季铵盐的浓度为8g/L,柠檬酸的浓度为12g/L。
5.如权利要求1或2或3或4所述抗皱棉麻织物的制备方法,其特征在于,步骤(2)中,所述处理温度为60℃。
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EP1118705A2 (en) * | 2000-01-18 | 2001-07-25 | Gunze Co., Ltd. | Fiber treating agents and methods of treating fibers |
JP2002069848A (ja) * | 2000-09-04 | 2002-03-08 | Gunze Ltd | 繊維処理剤、繊維の処理方法及び繊維製品 |
CN103174015A (zh) * | 2013-04-08 | 2013-06-26 | 太仓棨淂服装有限公司 | 纯棉牛仔布的壳聚糖季铵盐抗菌整理方法 |
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