CN110468592A - 一种羊毛面料的抗起毛整理方法 - Google Patents
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Abstract
本发明公开了一种羊毛面料的抗起毛整理方法,包括减法还原、聚氨酯预聚体的合成和加法整理步骤。该羊毛面料的抗起毛整理方法通过三羧乙基膦还原破坏羊毛纤维鳞片层,促使二硫键温和地还原为巯基,将合成的粘度较低的聚氨酯预聚体形成薄膜包覆纤维表面,结合减法处理和加法处理,改善羊毛面料的抗起毛效果。
Description
技术领域
本发明涉及面料抗起毛技术领域,具体涉及一种羊毛面料的抗起毛整理方法。
背景技术
羊毛面料的抗起毛起球的方法主要包括两大类,加法处理和减法处理,前者是指通过一定的方法将聚合物沉积在纤维表面,从而减少羊毛纤维表面的摩擦效应;而后者是指利用一定的化学方法将纤维表面的鳞片层剥落,进而提高羊毛的防毡缩效果。
减法处理的缺陷在于织物泛黄以及处理过程使用大量的化学试剂,基于环保角度考虑,工业废水的处理难度大。加法处理的羊毛织物能够确保良好的防毡缩性能和耐洗性,但纤维之间抱合力较差,容易在服装表面形成毛羽,影响织物的美观和服用性能。
发明内容
本发明的目的在于克服现有技术中存在的缺陷,提供一种羊毛面料的抗起毛整理方法,将现有的减法处理和加法处理相结合,达到抗起毛效果。
为实现上述目的,本发明的技术方案为:一种羊毛面料的抗起毛整理方法,其特征在于,包括以下步骤:
S1:将羊毛精纺面料置于乙醇溶液中清洗处理,烘干;
S2:将S1所得羊毛面料直接转移至还原液中,绝氧反应2~4h后,水洗烘干,还原液的主要组分为与水混溶的醇溶剂、三羧乙基膦、水和pH值调节剂,所述还原液的pH值范围为6.5~7.5;
S3:合成聚氨酯预聚体,将5重量份的异氰酸酯、8~10重量份的聚多元醇和0.1~0.3重量份的催化剂混匀并置于65~85℃下反应2~5h,然后降温至35~55℃向反应体系中加入具有羟基的0.5~1重量份的扩链剂,继续反应1~3h,加入2000~2500重量份有机溶剂得聚氨酯预聚体分散液;
S4:将S2所的羊毛面料浸渍于S3所得聚氨酯预聚体分散液中,加入三乙胺反应0.5~1h,低温烘干,得抗起毛的羊毛面料。
优选的技术方案为,S3中异氰酸酯为选自二苯基甲烷二异氰酸酯、4 ,4 '-二环己基甲烷二异氰酸酯、甲苯二异氰酸酯、异佛尔酮二异氰酸酯、六亚甲基二异氰酸酯中的一种或两种以上的组合,所述多元醇为选自聚丙二醇和/或聚乙二醇。
优选的技术方案为,还原液中水和醇溶剂的体积比为1:(4~6),三羧乙基膦的浓度为15~30mol/L。
优选的技术方案为,所述催化剂为二月桂酸二丁基锡,所述扩链剂为2,2-二羟甲基丙酸。
本发明的优点和有益效果在于:
该羊毛面料的抗起毛整理方法通过三羧乙基膦还原破坏羊毛纤维鳞片层,促使二硫键温和地还原为巯基,将合成的粘度较低的聚氨酯预聚体形成薄膜包覆纤维表面,结合减法处理和加法处理,改善羊毛面料的抗起毛效果。
具体实施方式
下面结合实施例,对本发明的具体实施方式作进一步描述。以下实施例仅用于更加清楚地说明本发明的技术方案,而不能以此来限制本发明的保护范围。
实施例1
实施例1羊毛面料的抗起毛整理方法包括以下步骤:
S1:将羊毛精纺面料置于乙醇溶液中清洗处理,烘干;
S2:将S1所得羊毛面料直接转移至还原液中,绝氧反应2h后,水洗烘干,还原液的主要组分为与水混溶的醇溶剂、三羧乙基膦、水和pH值缓冲对,还原液的pH值范围为6.5~7;
S3:合成聚氨酯预聚体,将5重量份的异氰酸酯、8重量份的聚多元醇和0.3重量份的催化剂混匀并置于65℃下反应5h,然后降温至35℃向反应体系中加入具有羟基的1重量份的扩链剂,继续反应1h,加入2500重量份有机溶剂得聚氨酯预聚体分散液;
S4:将S2所的羊毛面料浸渍于S3所得聚氨酯预聚体分散液中,加入1%( owf)三乙胺反应0.5h,低温烘干,得抗起毛的羊毛面料。
S3中异氰酸酯为异佛尔酮二异氰酸酯,多元醇为聚丙二醇。
还原液中水和醇溶剂的体积比为1:4,三羧乙基膦的浓度为30mol/L。
催化剂为二月桂酸二丁基锡,扩链剂为2,2-二羟甲基丙酸。
实施例2-3
实施例2-3基于实施例1,区别在于聚氨酯的合成工艺参数:
实施例2:将5重量份的异氰酸酯、8重量份的聚多元醇和0.3重量份的催化剂混匀并置于65℃下反应5h,然后降温至35℃向反应体系中加入具有羟基的1重量份的扩链剂,继续反应1h,加入2500重量份有机溶剂得聚氨酯预聚体分散液;
S3中异氰酸酯为二苯基甲烷二异氰酸酯,多元醇为聚乙二醇。
催化剂为二月桂酸二丁基锡和三乙烯二胺重量比1:2的混合物。扩链剂为乙二胺。
实施例3:将5重量份的异氰酸酯、9重量份的聚多元醇和0.2重量份的催化剂混匀并置于75℃下反应3h,然后降温至45℃向反应体系中加入具有羟基的1.7重量份的扩链剂,继续反应2h,加入2200重量份有机溶剂得聚氨酯预聚体分散液。
实施例4-5
实施例4-5基于实施例3,区别在于S2还原反应的工艺参数:
实施例4:绝氧反应4h,还原液的pH值范围为7~7.5,还原液中水和醇溶剂的体积比为1:6,三羧乙基膦的浓度为15mol/L。
实施例5:绝氧反应2~4h,还原液的pH值范围为7~7.5,还原液中水和醇溶剂的体积比为1:5,三羧乙基膦的浓度为20mol/L。
实施例1中采用碳酸钠/碳酸氢钠缓冲对或者磷酸氢二钠/磷酸二氢钠缓冲对调节还原液的pH值。
对比例
对比例为未经处理的羊毛面料。
采用耐磨及起毛起球试验仪测试实施例和对比例的羊毛面料的起毛性能:
摩擦125次时,对比例羊毛面料表面轻微起毛(4级),实施例1-6所得面料没有起毛变化(5级);
摩擦次数增加至500次,对比例羊毛面料起毛量增加,并具有少量毛球(3.5级),实施例1-6所得面料没有起毛变化(5级);
摩擦次数增加至1000次,对比例羊毛面料起毛量持续增加,实施例1-6所得面料没有起毛变化(5级),
摩擦次数进一步增加至7000次,实施例1-6所得面料表面轻微起毛(4级)。
以上所述仅是本发明的优选实施方式,应当指出,对于本技术领域的普通技术人员来说,在不脱离本发明技术原理的前提下,还可以做出若干改进和润饰,这些改进和润饰也应视为本发明的保护范围。
Claims (4)
1.一种羊毛面料的抗起毛整理方法,其特征在于,包括以下步骤:
S1:将羊毛精纺面料置于乙醇溶液中清洗处理,烘干;
S2:将S1所得羊毛面料直接转移至还原液中,绝氧反应2~4h后,水洗烘干,还原液的主要组分为与水混溶的醇溶剂、三羧乙基膦、水和pH值调节剂,所述还原液的pH值范围为6.5~7.5;
S3:合成聚氨酯预聚体,将5重量份的异氰酸酯、8~10重量份的聚多元醇和0.1~0.3重量份的催化剂混匀并置于65~85℃下反应2~5h,然后降温至35~55℃向反应体系中加入具有羟基的0.5~1重量份的扩链剂,继续反应1~3h,加入2000~2500重量份有机溶剂得聚氨酯预聚体分散液;
S4:将S2所的羊毛面料浸渍于S3所得聚氨酯预聚体分散液中,加入三乙胺反应0.5~1h,低温烘干,得抗起毛的羊毛面料。
2.根据权利要求1所述的羊毛面料的抗起毛整理方法,其特征在于,S3中异氰酸酯为选自二苯基甲烷二异氰酸酯、4 ,4 '-二环己基甲烷二异氰酸酯、甲苯二异氰酸酯、异佛尔酮二异氰酸酯、六亚甲基二异氰酸酯中的一种或两种以上的组合,所述多元醇为选自聚丙二醇和/或聚乙二醇。
3.根据权利要求1所述的羊毛面料的抗起毛整理方法,其特征在于,还原液中水和醇溶剂的体积比为1:(4~6),三羧乙基膦的浓度为15~30mol/L。
4.根据权利要求2所述的所述的羊毛面料的抗起毛整理方法,其特征在于,所述催化剂为二月桂酸二丁基锡,所述扩链剂为2,2-二羟甲基丙酸。
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CN113121774A (zh) * | 2021-04-07 | 2021-07-16 | 万华化学集团股份有限公司 | 一种聚氨酯跑道复合材料的制备工艺 |
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