CN112281525A - 一种扎染方法及其制得的银亮丝针织布 - Google Patents
一种扎染方法及其制得的银亮丝针织布 Download PDFInfo
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Abstract
本发明属于扎染技术领域,具体涉及一种扎染方法及其制得的银亮丝针织布。本发明扎染方法包括以下步骤,S1:布料的预处理;将布料依次进行碱混合液浸泡、第一次水清洗、生物酶混合液浸泡和第二次水清洗操作,取出晾干,熨烫平整,得到待处理布料;S2:捆扎或缝结布料;S3:染色;将步骤S2的扎结布料用水浸泡,晾至不滴水,再将扎结布料用染色液浸泡,重复染色;S4:将步骤S3已染色的扎结布料取出,用水震荡清洗,晾干,拆结,熨烫平整,即得。本发明的扎染方法在传统工艺进行了调整,布料依次进行碱混合液浸泡、第一次水清洗、生物酶混合液浸泡和第二次水清洗操作,再进行捆扎或缝结,以及染色后得到的布料,布面均匀,且具有较好的耐日晒色牢度。
Description
技术领域
本发明属于扎染技术领域,具体涉及一种扎染方法及其制得的银亮丝针织布。
背景技术
传统扎染技术是指先利用扎、结等防止染色的手法后,再进行染色,当这些扎、结部分被拆开后就显示处深浅不同的变化,其所出现的色调、光晕、肌理等都体现了扎染的艺术性。
现代扎染技术延续了传统扎染技术的大部分工艺,并将扎染与数码印花相结合,使得传统扎染技术得到了更广泛的应用。而对于现代的年轻人,对衣物在追求超潮流的同时,也不断地追求质感,这样的趋势下,使得扎染技术需要更加的成熟化,也要求扎染后具有更好的效果,如更牢固的色彩、更高的显色度、以及更均匀的色彩分布。
如中国专利CN109629272A公开了一种染色均匀的扎染方法,包括步骤为:选取布料,对所述布料采用α-淀粉酶、氯化钠和苯烷基磺酸钠的混合液进行退浆,再对退浆后的布料采用次氯酸钠漂白,晾干得到处理后的布料;按照待制得的花纹图案,对布料进行折叠并缠扎,得到扎结好的布料;将布料用水浸泡,再放入染料中染色,取出后晾干,再放入染料中染色,重复浸染多次后取出,其中所述染料包括;将布料清洗,将布料上的扎结处拆开,熨烫平整,得到包括花地的扎染布料。该发明通过上述方式,染色均匀,颜色明丽明快,层次丰富,色彩间的衔接处晕染的晕接自然,能够使布料的整体色调和谐统一,给人以美感的享受。
又如中国专利CN110485178A公开了一种提高间隔仿扎染凉感面料色牢度的方法,包括如下步骤:坯布→织物退浆→水洗、酸中和→烘干工艺→电晕处理→机械打折→涂料数码印花→成品定型。该发明采用电晕处理超高分子量聚乙烯面料,使PE由非极性转化为极性,使PE长丝表面粗化,增大表面活性,从而使产品的表面具有更强粘附力(即具有更高的达因系数),提高后续涂料印花的干湿摩擦牢度。
发明内容
本发明旨在提供一种扎染方法及其制得的银亮丝针织布,本发明的扎染方法,将布料依次进行碱混合液浸泡、第一次水清洗、生物酶混合液浸泡和第二次水清洗操作,再进行捆扎或缝结,以及染色后得到的布料,布面均匀,且具有较好的耐日晒色牢度。
为了达到上述目的,本发明采用以下技术方案:
一种扎染方法,包括以下步骤:
S1:布料的预处理;将布料依次进行碱混合液浸泡、第一次水清洗、生物酶混合液浸泡和第二次水清洗操作,取出晾干,熨烫平整,得到待处理布料;
S2:捆扎或缝结布料;根据扎染图案的形状和尺寸,在步骤S1的待处理布料上进行进行捆扎或缝结,得到扎结布料;
S3:染色;将步骤S2的扎结布料用水浸泡,晾至不滴水,再将扎结布料用染色液浸泡0.5~1.5h,重复染色2~5次;
S4:将步骤S3已染色的扎结布料取出,用水震荡清洗,震荡功率为100~150W,晾干,再将扎结布料拆开,熨烫平整,即得。
优选地,所述步骤S1布料与碱混合液的重量比为1:(5~15),布料与生物酶混合液的重量比为1:(5~15);所述步骤S3中扎结布料与染色液的重量比为1:(5~15)。
优选地,所述步骤S3中染色液的组成包括以下组分:羟乙纤维素2~5份、着色剂5~8份、油酸钠8~13份、山嵛基三甲基铵甲基硫酸盐3~9份、植酸1~3份和水70~110份。
优选地,所述染色液的制备方法为:取水和羟乙纤维素、油酸钠、三甲基铵甲基硫酸盐混合搅拌20~35min,再依次加入着色剂和植酸,即得。
优选地,所述着色剂包括翠兰S-GL或活性艳红HE-3B。
优选地,所述步骤S1中碱混合液浸泡的温度为60~95℃,浸泡时间为5~10min。
优选地,所述碱混合液的组成包括以下组分:氢氧化钠0.5~1.5份、双氧水0.5~1.5份、异丙醇5~10份、葡萄糖酸亚铁0.3~0.7份和水85~95份。
优选地,所述步骤S1中生物酶混合液的浸泡时间为30~120min,温度为40~50℃,所述生物酶混合液为含有α-淀粉酶和氯化钠的水溶液。
优选地,所述α-淀粉酶、氯化钠与水的质量比为1:(0.2~0.35):(10~20)。
本发明另一目的是提供上述方法制得的银亮丝针织布。
与现有技术相比,本发明具有以下有益效果:
(1)本发明的扎染方法在传统工艺进行了调整,布料依次进行碱混合液浸泡、第一次水清洗、生物酶混合液浸泡和第二次水清洗操作能够对布料实现较好的整体退浆,促使布料在后部分的染色步骤中易于染色和均匀染色。
(2)本发明的扎染方法在染色剂加入植酸和三甲基铵甲基硫酸盐共同作用,促使着色剂可以缓慢均匀地与布料相接触,避免局部过重而导致的不均匀,并使着色剂很好的布料结合,经实验二表明,扎染后的布料具有较好的耐日晒色牢度。
具体实施方式
以下通过实施例形式的具体实施方式,对本发明的上述内容作进一步的详细说明。但不应将此理解为本发明上述主题的范围仅限于以下实施例。
在本发明的实施例1~3和对比例1~2中,布料为棉针织布;实施例3的布料为银亮丝针织布。在本发明的扎染方法中,步骤S1布料与碱混合液的重量比为1:8,布料与生物酶混合液的重量比为1:8;所述步骤S3中扎结布料与染色液的重量比为1:8。
实施例1、一种扎染方法
包括以下步骤:
S1:布料的预处理;将布料依次进行碱混合液浸泡(浸泡的温度为90℃,浸泡时间为5min)、第一次水清洗、生物酶混合液浸泡(浸泡时间为60min,温度为40℃)和第二次水清洗操作,取出晾干,熨烫平整,得到待处理布料;
S2:捆扎或缝结布料;根据扎染图案的形状和尺寸,在步骤S1的待处理布料上进行进行捆扎或缝结,得到扎结布料;
S3:染色;将步骤S2的扎结布料用水浸泡,晾至不滴水,再将扎结布料用染色液浸泡0.5h,重复染色3次;
S4:将步骤S3已染色的扎结布料取出,用水震荡清洗,震荡功率为100W,晾干,再将扎结布料拆开,熨烫平整,即得。
其中,
步骤S3中染色液的组成为:羟乙纤维素3份、着色剂5份、油酸钠8份、山嵛基三甲基铵甲基硫酸盐3份、植酸2份和水80份。染色液的制备方法为:取水和羟乙纤维素、油酸钠、三甲基铵甲基硫酸盐混合搅拌20min,再依次加入着色剂和植酸,即得。
着色剂为翠兰S-GL。
步骤S1中碱混合液的组成为:氢氧化钠0.5份、双氧水0.8份、异丙醇8份、葡萄糖酸亚铁0.3份和水88份。
步骤S1中生物酶混合液为含有α-淀粉酶和氯化钠的水溶液,α-淀粉酶、氯化钠与水的质量比为1:0.3:20。
实施例2、一种扎染方法
包括以下步骤:
S1:布料的预处理;将布料依次进行碱混合液浸泡(浸泡的温度为88℃,浸泡时间为5min)、第一次水清洗、生物酶混合液浸泡(浸泡时间为55min,温度为45℃)和第二次水清洗操作,取出晾干,熨烫平整,得到待处理布料;
S2:捆扎或缝结布料;根据扎染图案的形状和尺寸,在步骤S1的待处理布料上进行进行捆扎或缝结,得到扎结布料;
S3:染色;将步骤S2的扎结布料用水浸泡,晾至不滴水,再将扎结布料用染色液浸泡0.5h,重复染色2次;
S4:将步骤S3已染色的扎结布料取出,用水震荡清洗,震荡功率为100W,晾干,再将扎结布料拆开,熨烫平整,即得。
其中,
步骤S3中染色液的组成为:羟乙纤维素3份、着色剂6份、油酸钠8份、山嵛基三甲基铵甲基硫酸盐4份、植酸2份和水90份。染色液的制备方法为:取水和羟乙纤维素、油酸钠、三甲基铵甲基硫酸盐混合搅拌25min,再依次加入着色剂和植酸,即得。
着色剂包括翠兰S-GL。
步骤S1中碱混合液的组成为:氢氧化钠0.75份、双氧水0.75份、异丙醇7.5份、葡萄糖酸亚铁0.35份和水85份。
步骤S1中生物酶混合液为含有α-淀粉酶和氯化钠的水溶液,α-淀粉酶、氯化钠与水的质量比为1:0.3:20。
实施例3、一种扎染方法
包括以下步骤:
S1:布料的预处理;将布料依次进行碱混合液浸泡(浸泡的温度为89℃,浸泡时间为5min)、第一次水清洗、生物酶混合液浸泡(浸泡时间为55min,温度为45℃)和第二次水清洗操作,取出晾干,熨烫平整,得到待处理布料;
S2:捆扎或缝结布料;根据扎染图案的形状和尺寸,在步骤S1的待处理布料上进行进行捆扎或缝结,得到扎结布料;
S3:染色;将步骤S2的扎结布料用水浸泡,晾至不滴水,再将扎结布料用染色液浸泡0.5~1.5h,重复染色2~5次;
S4:将步骤S3已染色的扎结布料取出,用水震荡清洗,震荡功率为100~150W,晾干,再将扎结布料拆开,熨烫平整,即得。
其中,
步骤S3中染色液的组成为:羟乙纤维素3份、着色剂6份、油酸钠8份、山嵛基三甲基铵甲基硫酸盐3.5份、植酸1.5份和水80份。染色液的制备方法为:取水和羟乙纤维素、油酸钠、三甲基铵甲基硫酸盐混合搅拌30min,再依次加入着色剂和植酸,即得。
着色剂为活性艳红HE-3B。
步骤S1中碱混合液的组成为:氢氧化钠1份、双氧水1份、异丙醇8份、葡萄糖酸亚铁0.4份和水90份。
步骤S1中生物酶混合液为含有α-淀粉酶和氯化钠的水溶液,α-淀粉酶、氯化钠与水的质量比为1:0.3:18。
实施例4、一种扎染方法
包括以下步骤:
S1:布料的预处理;将布料依次进行碱混合液浸泡(浸泡的温度为90℃,浸泡时间为7min)、第一次水清洗、生物酶混合液浸泡(浸泡时间为55min,温度为45℃)和第二次水清洗操作,取出晾干,熨烫平整,得到待处理布料;
S2:捆扎或缝结布料;根据扎染图案的形状和尺寸,在步骤S1的待处理布料上进行进行捆扎或缝结,得到扎结布料;
S3:染色;将步骤S2的扎结布料用水浸泡,晾至不滴水,再将扎结布料用染色液浸泡0.5h,重复染色3次;
S4:将步骤S3已染色的扎结布料取出,用水震荡清洗,震荡功率为100W,晾干,再将扎结布料拆开,熨烫平整,即得。
其中,
步骤S3中染色液的组成为:羟乙纤维素3份、着色剂6份、油酸钠9份、山嵛基三甲基铵甲基硫酸盐3.5份、植酸2份和水90份。染色液的制备方法为:取水和羟乙纤维素、油酸钠、三甲基铵甲基硫酸盐混合搅拌30min,再依次加入着色剂和植酸,即得。
着色剂为活性艳红HE-3B。
步骤S1中碱混合液的组成为:氢氧化钠1份、双氧水0.8份、异丙醇8份、葡萄糖酸亚铁0.3份和水90份。
步骤S1中生物酶混合液为含有α-淀粉酶和氯化钠的水溶液,α-淀粉酶、氯化钠与水的质量比为1:0.25:20。
对比例1、一种扎染方法
包括以下步骤:
S1:布料的预处理;将布料依次进行碱混合液浸泡(浸泡的温度为88℃,浸泡时间为5min)、第一次水清洗、生物酶混合液浸泡(浸泡时间为55min,温度为45℃)和第二次水清洗操作,取出晾干,熨烫平整,得到待处理布料;
S2:捆扎或缝结布料;根据扎染图案的形状和尺寸,在步骤S1的待处理布料上进行进行捆扎或缝结,得到扎结布料;
S3:染色;将步骤S2的扎结布料用水浸泡,晾至不滴水,再将扎结布料用染色液浸泡0.5h,重复染色2次;
S4:将步骤S3已染色的扎结布料取出,用水震荡清洗,震荡功率为100W,晾干,再将扎结布料拆开,熨烫平整,即得。
其中,
步骤S3中染色液的组成为:羟乙纤维素3份、着色剂6份、油酸钠8份、山嵛基三甲基铵甲基硫酸盐4份和水90份。染色液的制备方法为:取水和羟乙纤维素、油酸钠、三甲基铵甲基硫酸盐混合搅拌25min,再加入着色剂,即得。
着色剂包括翠兰S-GL。
步骤S1中碱混合液的组成为:氢氧化钠0.75份、双氧水0.75份、异丙醇7.5份、葡萄糖酸亚铁0.35份和水85份。
步骤S1中生物酶混合液为含有α-淀粉酶和氯化钠的水溶液,α-淀粉酶、氯化钠与水的质量比为1:0.3:20。
本对比例与实施例2的区别在于,未加入植酸。
对比例2、一种扎染方法
包括以下步骤:
S1:布料的预处理;将布料依次进行碱混合液浸泡(浸泡的温度为88℃,浸泡时间为5min)、第一次水清洗、生物酶混合液浸泡(浸泡时间为55min,温度为45℃)和第二次水清洗操作,取出晾干,熨烫平整,得到待处理布料;
S2:捆扎或缝结布料;根据扎染图案的形状和尺寸,在步骤S1的待处理布料上进行进行捆扎或缝结,得到扎结布料;
S3:染色;将步骤S2的扎结布料用水浸泡,晾至不滴水,再将扎结布料用染色液浸泡0.5h,重复染色2次;
S4:将步骤S3已染色的扎结布料取出,用水震荡清洗,震荡功率为100W,晾干,再将扎结布料拆开,熨烫平整,即得。
其中,
步骤S3中染色液的组成为:羟乙纤维素3份、着色剂6份、油酸钠8份、植酸2份和水90份。染色液的制备方法为:取水和羟乙纤维素、油酸钠混合搅拌25min,再依次加入着色剂和植酸,即得。
着色剂包括翠兰S-GL。
步骤S1中碱混合液的组成为:氢氧化钠0.75份、双氧水0.75份、异丙醇7.5份、葡萄糖酸亚铁0.35份和水85份。
步骤S1中生物酶混合液为含有α-淀粉酶和氯化钠的水溶液,α-淀粉酶、氯化钠与水的质量比为1:0.3:20。
本对比例与实施例2的区别在于,未加入三甲基铵甲基硫酸盐。
对比例3、一种扎染方法
包括以下步骤:
S1:布料的预处理;将布料依次进行碱混合液浸泡(浸泡的温度为88℃,浸泡时间为5min)、第一次水清洗、生物酶混合液浸泡(浸泡时间为55min,温度为45℃)和第二次水清洗操作,取出晾干,熨烫平整,得到待处理布料;
S2:捆扎或缝结布料;根据扎染图案的形状和尺寸,在步骤S1的待处理布料上进行进行捆扎或缝结,得到扎结布料;
S3:染色;将步骤S2的扎结布料用水浸泡,晾至不滴水,再将扎结布料用染色液浸泡0.5h,重复染色2次;
S4:将步骤S3已染色的扎结布料取出,用水震荡清洗,震荡功率为100W,晾干,再将扎结布料拆开,熨烫平整,即得。
其中,
步骤S3中染色液的组成为:羟乙纤维素3份、着色剂6份、油酸钠12份、植酸2份和水90份。染色液的制备方法为:取水和羟乙纤维素、油酸钠混合搅拌25min,再依次加入着色剂和植酸,即得。
着色剂包括翠兰S-GL。
步骤S1中碱混合液的组成为:氢氧化钠0.75份、双氧水0.75份、异丙醇7.5份、葡萄糖酸亚铁0.35份和水85份。
步骤S1中生物酶混合液为含有α-淀粉酶和氯化钠的水溶液,α-淀粉酶、氯化钠与水的质量比为1:0.3:20。
本对比例与实施例2的区别在于,未加入三甲基铵甲基硫酸盐,且油钠酸为12份。
实验一、色彩均匀性的测定
实验方法:按照实施例/对比例的染色方法制得针织布,观察布面需染色的效果。
表1观察结果
从表1可以看出,实施例1~4的针织布色彩均匀,色彩间衔接处自然,布面没有出现斑驳现象。
实验二、色彩牢固性的测定
实验方法:按照GB/T 8427-2008《纺织品色牢度试验耐人造光色牢度:氙弧》测试,再按照GB/T 250-2008《纺织品色牢度试验评定变色用灰色样卡》测定变色等级。
表2变色测试结果
从表2可以看出,实施例1~4耐日晒色牢固好,对比例1和对比例2的耐日晒色牢度下降,提示植酸有利于提高布料的耐日晒色牢度,而当不加入三甲基铵甲基硫酸盐时,布料的耐日晒色牢度下降。
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 (8)
1.一种扎染方法,其特征在于,包括以下步骤:
S1:布料的预处理;将布料依次进行碱混合液浸泡、第一次水清洗、生物酶混合液浸泡和第二次水清洗操作,取出晾干,熨烫平整,得到待处理布料;
S2:捆扎或缝结布料;根据扎染图案的形状和尺寸,在步骤S1的待处理布料上进行进行捆扎或缝结,得到扎结布料;
S3:染色;将步骤S2的扎结布料用水浸泡,晾至不滴水,再将扎结布料用染色液浸泡0.5~1.5h,重复染色2~5次;
S4:将步骤S3已染色的扎结布料取出,用水震荡清洗,震荡功率为100~150W,晾干,再将扎结布料拆开,熨烫平整,即得。
2.根据权利要求1所述扎染方法,其特征在于,所述步骤S3中染色液的组成包括以下组分:羟乙纤维素2~5份、着色剂5~8份、油酸钠8~13份、山嵛基三甲基铵甲基硫酸盐3~9份、植酸1~3份和水70~110份。
3.根据权利要求1所述扎染方法,其特征在于,所述染色液的制备方法为:取水和羟乙纤维素、油酸钠、三甲基铵甲基硫酸盐混合搅拌20~35min,再依次加入着色剂和植酸,即得。
4.根据权利要求1所述扎染方法,其特征在于,所述步骤S1中碱混合液浸泡的温度为60~95℃,浸泡时间为5~10min。
5.根据权利要求1或4所述扎染方法,其特征在于,所述碱混合液的组成包括以下组分:氢氧化钠0.5~1.5份、双氧水0.5~1.5份、异丙醇5~10份、葡萄糖酸亚铁0.3~0.7份和水85~95份。
6.根据权利要求1所述扎染方法,其特征在于,所述步骤S1中生物酶混合液的浸泡时间为30~120min,温度为40~50℃,所述生物酶混合液为含有α-淀粉酶和氯化钠的水溶液。
7.根据权利要求5所述扎染方法,其特征在于,所述α-淀粉酶、氯化钠与水的质量比为1:(0.2~0.35):(10~20)。
8.根据权利要求1~7任一所述方法制得的银亮丝针织布。
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