CN102232129A - 一种将特性赋予剂加料至聚合物产物的方法 - Google Patents
一种将特性赋予剂加料至聚合物产物的方法 Download PDFInfo
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- CN102232129A CN102232129A CN2009801446318A CN200980144631A CN102232129A CN 102232129 A CN102232129 A CN 102232129A CN 2009801446318 A CN2009801446318 A CN 2009801446318A CN 200980144631 A CN200980144631 A CN 200980144631A CN 102232129 A CN102232129 A CN 102232129A
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Abstract
本发明设计一种将属性赋予剂加料至聚合产物的方法、由该方法制成的聚合产物以及一种用于制备能够长期保留所获得属性的聚合产物的组合物。
Description
发明领域
本发明涉及一种将特性赋予剂加料至聚合物产物的方法、由该方法制成的聚合物产物以及一种用于制备聚合物产物的组合物。
发明背景
具特性的聚合物产物为多种应用所需。为了赋予这些特性,通常用具这些特性的活性成分来处理这些聚合物产物。在这些处理之前,通常对聚合物产物进行表面加工以使其可以结合活性成分。然而,加工过的表面上这些活性成分通常不能很好保留,并且在随后的处理如洗涤、漂白等中这些聚合物产物失去其活性。
US 2008/003218揭露了一种以微胶囊形式将活性成分应用于聚合物纺丝原液的方法。通过这种应用方法,尽管活性成分在纤维中保留较长一段时间,但是一旦活性成分从包封剂中排出,就不能补充活性成分,因此降低其有效性。
希望有一种将特性赋予剂加料至聚合物产物的方法,其中该方法将使加料过的聚合物产物能将所获得的特性维持很长时间。
发明详细说明
因此,本发明提供一种能够延长保留所获得的特性的聚合物产物的加料方法。
本发明说明书中所用的以下术语具有以下含义:
本文中所用的术语“特性赋予剂”是指能够赋予特性例如颜色、气味等,或能赋予功能特性如抗菌活性、紫外辐射屏障、抗皱等的原子、离子、原子组或离子组、化合物或化合物混合物。
本文中所用的术语“所获得的特性”是指从特性赋予剂所获得的特性。
本文中所用的术语“非极性有机储集体”是指高分子量烃或其衍生物,包括石蜡、硬脂醇、十四烷醇及其类似物。
本文中所用的术语“包封”是指密封在聚合物壳内。
本文中所用的术语“未包封”是指未完全密封在聚合物壳内。
本文中所定义的术语“纺丝原液(dope)”是指溶液、浆料或聚合物组合物。
在一个实施方案中,本发明提供一种将特性赋予剂加料至聚合物产物的方法,该方法包括:首先使聚合物纺丝原液或其前体与含有未包封非极性有机储集体的乳液接触,以形成包含纺丝原液和乳液的可纺组合物,然后通过模头/喷丝头纺织该组合物,以形成带有能够延长特性赋予剂保留的储集体的再生复合材料,最后使该复合材料或其产物与包含至少一种特性赋予剂和溶胀剂的配制剂在大于或等于储集体熔点/软化点的温度下接触至少10分钟。
在另一实施方案中,本发明提供一种将特性赋予剂加料至聚合物产物的方法,该方法包括:首先使聚合物纺丝原液或其前体与含有未包封非极性有机储集体的乳液接触,以形成包含纺丝原液和乳液的可纺组合物,然后通过模头/喷丝头纺织该组合物,以形成带有能够延长特性赋予剂保留的非极性有机储集体的再生复合材料,并且最后使该复合材料或其产物与包含至少一种特性赋予剂和溶胀剂的配制剂在大于或等于储集体熔点/软化点的温度下接触至少10分钟,其中聚合物纺丝原液选自由粘胶纺丝原液、丙烯酸纺丝原液及纤维素纺丝原液组成的群组。
在另一实施方案中,本发明提供一种将特性赋予剂加料至聚合物产物的方法,该方法包括:首先使聚合物纺丝原液或其前体与含有未包封非极性有机储集体的乳液接触,以形成包含纺丝原液和乳液的可纺组合物,然后通过模头/喷丝头纺织该组合物,以形成带有能够延长特性赋予剂保留的非极性有机储集体的再生复合材料,最后使该复合材料或其产物与包含至少一种特性赋予剂和溶胀剂的配制剂在大于或等于储集体熔点/软化点的温度下接触至少10分钟,其中非极性有机储集体为熔点在10-120℃范围内的链烷烃、有机醇、有机脂肪酸或其酯、聚乙烯或其任何混合物。
在另一实施方案中,本发明提供一种将特性赋予剂加料至聚合物产物的方法,该方法包括:首先使聚合物纺丝原液或其前体与含有未包封非极性有机储集体的乳液接触,以形成包含纺丝原液和乳液的可纺组合物,然后通过模头/喷丝头纺织该组合物,以形成带有能够延长特性赋予剂保留的非极性有机储集体的再生复合材料,最后使该复合材料或其产物与包含至少一种特性赋予剂和溶胀剂的配制剂在大于或等于储集体熔点/软化点的温度下接触至少10分钟,其中复合材料与包含0.0001至15%特性赋予剂、0.01至99.999%溶胀剂及0.0001至15%表面活性剂的水性配制剂接触。
在另一实施方案中,本发明提供一种将特性赋予剂加料至聚合物产物的方法,该方法包括:首先使聚合物纺丝原液或其前体与含有未包封非极性有机储集体的乳液接触,以形成包含纺丝原液和乳液的可纺组合物,然后通过模头/喷丝头纺织该组合物,以形成带有能够延长特性赋予剂保留的非极性有机储集体的再生复合材料,最后使该复合材料或其产物与包含至少一种特性赋予剂和溶胀剂的配制剂在大于或等于储集体熔点/软化点的温度下接触至少10分钟,其中表面活性剂选自由离子型表面活性剂、非离子表面活性剂、两性表面活性剂和聚合物表面活性剂组成的群组。
在另一实施方案中,本发明提供一种将特性赋予剂加料至聚合物产物的方法,该方法包括:首先使聚合物纺丝原液或其前体与含有未包封非极性有机储集体的乳液接触,以形成包含纺丝原液和乳液的可纺组合物,然后通过模头/喷丝头纺织该组合物,以形成带有能够延长特性赋予剂保留的非极性有机储集体的再生复合材料,最后使该复合材料或其产物与包含至少一种特性赋予剂和溶胀剂的配制剂在大于或等于储集体熔点/软化点的温度下接触至少10分钟,其中特性赋予剂为抗微生物剂、杀真菌剂、杀菌剂、灭藻剂、治疗剂、芳香族化合物、杀虫剂、杀螨剂、杀线虫剂、抗皱剂、柔软剂、抗氧化剂、阻燃剂、填料、补强剂、紫外防护剂、增塑剂、水运输剂/吸水剂、油溶性维生素、有机染料、着色剂或其任何混合物。
在另一实施方案中,本发明提供一种将特性赋予剂加料至聚合物产物的方法,该方法包括:首先使聚合物纺丝原液或其前体与含有未包封非极性有机储集体的乳液接触,以形成包含纺丝原液和乳液的可纺组合物,然后通过模头/喷丝头纺织该组合物,以形成带有能够延长特性赋予剂保留的非极性有机储集体的再生复合材料,最后使该复合材料或其产物与包含至少一种特性赋予剂和溶胀剂的配制剂在大于或等于储集体熔点/软化点的温度下接触至少10分钟,其中溶胀剂选自由以下各物组成的群组:水、环己醇、正戊胺、正戊醇、1,5-二氨基戊烷、甘油、苯酚、苯甲醇、间甲苯胺、间甲酚、2-乙基苯酚、苄胺、苯胺、乙基苯胺、聚苯乙烯、酯/酚、乙腈、邻硝基苯酚、对硝基苯酚、二甲基甲酰胺、二甲亚砜、邻苯基苯酚、碳酸亚乙酯、碳酸亚丙酯、硝基甲烷、异戊醇、氢氧化钾、溶纤剂、甲基溶纤剂、异丙醇、丙醇和间甲酚。
在另一实施方案中,本发明提供一种将特性赋予剂加料至聚合物产物的方法,该方法包括:首先使聚合物纺丝原液或其前体与含有未包封非极性有机储集体的乳液接触,以形成包含纺丝原液和乳液的可纺组合物,然后通过模头/喷丝头纺织该组合物,以形成带有能够延长特性赋予剂保留的非极性有机储集体的再生复合材料,最后使该复合材料或其产物与包含至少一种特性赋予剂和溶胀剂的配制剂在大于或等于储集体熔点/软化点的温度下接触至少10分钟,其中复合材料与配制剂的重量比在1∶1至1∶500范围内。
在另一实施方案中,本发明提供一种将特性赋予剂加料至聚合物产物的方法,该方法包括:首先使聚合物纺丝原液或其前体与含有未包封非极性有机储集体的乳液接触,以形成包含纺丝原液和乳液的可纺组合物,然后通过模头/喷丝头纺织该组合物,以形成带有能够延长特性赋予剂保留的非极性有机储集体的复合材料,最后使该复合材料或其产物与包含至少一种特性赋予剂和溶胀剂的配制剂在大于或等于储集体熔点/软化点的温度下接触至少10分钟,其中比例在1∶5至1∶100范围内。
在另一实施方案中,本发明提供一种包含未包封非极性有机储集体的加料聚合物产物,该非极性有机储集体保留至少一种在非极性有机储集体中溶解度大于1%的特性赋予剂。
在另一实施方案中,本发明提供一种能够延长保留所获得的特性的聚合物产物,该产物包含保留至少一种特性赋予剂的未包封非极性有机储集体,其中被保留的特性赋予剂至多为储集体和所保留特性赋予剂总重的60%。
在另一实施方案中,本发明提供一种能够延长保留所获得的特性的聚合物产物,该产物包含保留至少一种特性赋予剂的未包封非极性有机储集体,其中特性赋予剂为抗微生物剂、杀真菌剂、杀菌剂、灭藻剂、治疗剂、芳香化合物、杀虫剂、杀螨剂、杀线虫剂、抗皱剂、柔软剂、抗氧化剂、阻燃剂、填料、补强剂、紫外防护剂、增塑剂、水运输剂/吸水剂、油溶性维生素、有机染料、着色剂或其任何混合物。
在另一实施方案中,本发明提供一种遵循AATCC程序在AATCC标准参照洗涤剂存在下,在洗衣机内洗涤超过20次之后保留所获得的特性的聚合物产物。
在另一实施方案中,本发明提供一种适于在漂白、染色、预缩、固化或树脂处理之后保留所获得的特性的聚合物产物。
在另一实施方案中,本发明提供一种能够延长保留所获得的特性的聚合物产物,其中该聚合物产物能够持续/受控释放特性赋予剂。
在另一实施方案中,本发明提供一种能够延长保留所获得的特性的聚合物产物,其中特性赋予剂的释放受温度控制。
在另一实施方案中,本发明提供一种用于制备能够延长保留所获得的特性的聚合物产物的组合物,该组合物包含聚合物纺丝原液和熔点在10℃至120℃范围内的未包封非极性有机储集体。
在另一实施方案中,本发明提供一种用于制备能够延长保留所获得的特性的聚合物产物的组合物,该组合物包含聚合物纺丝原液和熔点在10℃至120℃范围内的未包封非极性有机储集体,其中聚合物纺丝原液为含有7-15%黄原酸盐形式的纤维素的粘胶纺丝原液。
在另一实施方案中,本发明提供一种用于制备能够延长保留所获得的特性的聚合物产物的组合物,该组合物包含聚合物纺丝原液和熔点在10℃至120℃范围内的未包封非极性有机储集体,其中聚合物纺丝原液为含有5-25%纤维素N-甲基氧化吗啉的纤维素纺丝原液或具有式I的离子液体。
其中R1与R3各自相互独立地为具有1至20个碳原子的有机剩余结构部分,R2、R4和R5各自相互独立地为H原子或具有1至20个碳原子的有机基团,X为阴离子,如卤化物、式Ra-COO-的羧酸盐阴离子,而Ra为C1至C20烷基,n为1、2或3。
在另一实施方案中,本发明提供一种用于制备能够延长保留所获得的特性的聚合物产物的组合物,该组合物包含聚合物纺丝原液和熔点在10℃至120℃范围内的未包封非极性有机储集体,其中聚合物纺丝原液为选自丙烯酸聚合物、单丙烯酸聚合物或其共混物的丙烯酸纺丝原液。
在另一实施方案中,本发明提供由该聚合物产物制成的织造织物、针织织物或非织造织物。
在另一实施方案中,本文明提供一种由超过5%的聚合物产物与其他天然、人造或合成纤维,例如聚酯、棉、羊毛、莱卡(lycra)、丝绸和亚麻共混制成的织造织物、针织织物或非织造织物。
在另一实施方案中,本发明提供一种由织物制成的物体或产品。
本发明提供一种聚合物产物,其具有未包封非极性有机物帮助长时间保留聚合物产物的所获得的特性。这些特性通过用特性赋予剂处理聚合物产物而获得。特性赋予剂通常包括但不限于:抗微生物剂,包括对羟基苯甲酸酯类(例如对羟基苯甲酸甲酯、对羟基苯甲酸乙酯、对羟基苯甲酸丙酯及对羟基苯甲酸丁酯)、噻唑化合物(例如4,5-二氯-正辛基-4-异噻唑啉-3-酮(DCOIT)、2-正辛基-4-异噻唑啉-3-酮(OIT)、苯并异噻唑啉酮(BIT))、基于咪唑的化合物(例如1-[(2-氯苯基)(二苯基)甲基]-1H-咪唑(克霉唑))、卤素-O-羟基-二苯基化合物(例如5-氯-2-(2,4-二氯苯氧基)苯酚(三氯生)、2,4,4′-三氯-2′-乙酰氧基-二苯醚(乙酸三氯生))、硫代氨基甲酸酯(例如o-(2-萘基)甲基(3-甲基苯基)硫代氨基甲酸酯(托萘酯)、二碘代甲基对甲苯砜)、酚衍生物(例如五氯酚、氯喹那啶醇、4-氯-3,5-二甲苯酚、苯氧基乙醇、1-苯氧基丙-2-醇)、双氯苯双胍己烷(chlorhexidine)及其衍生物、三对称二苯硫脲(trihalocarbanilide)衍生物;常用于香料的化合物,包括酚类化合物、精油、醛、酮、多环化合物、酯及醇;木质香料成分,包括雪松油(精油)、愈创木油(精油)、γ紫罗兰酮(酮)、檀香油(精油)及甲基柏木酮(酮);芳香香料成分,包括香豆素(酮)、香草醛(4-羟基-3-甲氧基苯甲醛)(醛)、乙基麦芽酚(醇)、苯乙醛(醛)、胡椒醛(醛)、苯乙酮(酮)及二氢香豆素(酮);柑橘芳香成分,包括橙油(精油)、柠檬油(精油)、柠檬醛(醛)、β甲基萘酮(酮)、乙酸松油酯(酯)、壬醛(醛)、松油醇(醇)及二氢月桂烯醇(醇);花香成分,包括多种植物亚类,例如玫瑰、薰衣草、茉莉、铃兰;玫瑰香料成分,包括乙酸香叶酯(酯)、香叶醇(醇)、香茅醇乙酸酯(酯)、苯乙醇(醇)、α二氢大马酮(酮)、β二氢大马酮(酮)、香叶油(精油)及天然玫瑰油(精油);薰衣草香料成分,包括二氢乙酸松油酯(酯)、乙基己基酮(酮)、杂薰衣草(lavandin)(精油)、薰衣草(精油)、四氢芳樟醇(醇)、芳樟醇(醇)和乙酸芳樟酯(酯);茉莉香料成分,包括乙酸苄酯(酯)、丁基肉桂醛(醛)、苯甲酸甲酯(酯)、天然茉莉油(精油)、二氢茉莉酮酸甲酯(酯);铃兰香料成分,包括仙客来醛(醛)、水杨酸苄酯(酯)、羟基香茅醇(醇)、香茅基含氧乙醛(醛)和羟基醛(醛);果味香料成分,包括丁酸乙基-2-甲基酯(酯)、环己烷丙酸烯丙酯(酯)、乙酸戊酯(酯)、乙酸乙酯(酯)、γ-癸内酯(酮)、辛内酯(octaiactone)(酮)、十一烷酸内酯(醛)、乙酰乙酸乙酯(酯)、苯甲醛(醛);动物香料成分,包括乙酸甲基苯基酯(酯)、吲哚(2,3-苯并吡咯)(酚类)、甲氧甲酚(酚类)、异丁基喹啉(酚类)和雄烯醇(酚类);香料香精成分,包括对甲氧基苯甲醛(醛)、八角茴香(精油)、丁子香油(精油)、丁子香酚(酚类)、异丁子香酚(酚类)、麝香草酚(酚类)、茴香脑(酚类)、肉桂醇(醇)和肉桂醛(醛);绿色香料成分,包括βγ己烯醇(醇)、溴苯乙烯(醇)、二甲基苄基甲醇(醇)、庚炔碳酸甲酯(酯)、乙酸顺-3-己烯酯(酯)和格蓬油(精油);麝香香料成分,包括加乐麝香(酚)、环十五烷内酯(酚)、麝香酮(酮)、黄葵内酯(酚)、吐纳麝香(酚)及巴西酸亚乙酯(酯);香膏香精成分,包括加拿大香脂(精油)、秘鲁香脂(精油)和安息香树脂(精油);薄荷香料成分,包括左旋香芹酮(酮)、薄荷醇(醇)、水杨酸甲酯(酯)、薄荷油(pepper mint oil)(精油)、薄荷油(spearmint oil)(精油)、桉树(精油)、乙酸茴香酯(酯)、甲基佳味醇(醇);化学香料成分,包括苯甲醇(醇)、一缩二丙二醇(醇)、乙醇(醇)和苯甲酸苄酯(酯);环氧柏木烷、柏木甲醚、癸基甲基醚、加乐麝香、龙涎醚(Grisalva)、吲哚芬(Indolarome)固体、橙花醚、Ozofleur、Phenafleur、Tobacarol、对甲酚甲醚、卡拉花醛(Karanal)、环格蓬酯(Cyclogalbanate)、异长叶烷酮(Piconia)、异龙涎酮(Iso-cyclemone)、龙涎酮(Iso E super)、萨利麝香(Celestolide)固体、庚基环戊酮、二氢异茉莉酮、异茉莉酮、吐纳麝香、甲基紫罗酮、胡椒基丙酮(Dulcinyl)固体、对甲氧基苯乙酮、Vetikone、十一烯醛、铃兰醛、香草醛、肉桂醇、异丁子香酚、四氢香叶醇、西瓜酮(Calone)、二氢茉莉酮、加乐麝香、卡拉花醛、β-萘基甲基醚(Nerolin)、癸基甲基醚、苯基甲基缩水甘油酸乙酯、苯乙酸对甲酚酯、十一碳烷酸内酯、Clonal IFF;杀虫剂/驱虫剂,如拟除虫菊酯;有机硫代磷酸盐类杀虫剂,如马拉硫磷、甲基嘧啶磷;有机氯化合物,如二氯二苯基三氯乙烷、新烟碱类杀虫剂(Neonicotinoids)、埃卡瑞丁(icaridin);精油,如爪哇香茅油、柠檬草油、雪松油、茶树油、桉树油;杀螨剂,如氯菊酯;油溶性维生素,如维生素A(视黄醇、棕榈酸酯)、维生素D前体(麦角甾醇)、维生素E(生育酚-α-生育酚和生育酚乙酸酯,及三烯生育酚)、维生素E乙酸酯和维生素K(甲基萘醌、2-甲基-1,4-萘醌衍生物及叶绿醌);柔软剂或润肤剂,如芦荟;皮肤增白剂,如4-丁基-1,3-二羟基苯(微溶于水);抗皱的或抗老化的分子,如1,4-双(3,4-二羟基苯基)-2-3-二甲基丁烷;抗紫外线化学品,如2-羟基-4-甲氧基二苯甲酮、2-氰基-3,3-二苯基丙烯酸2-乙基己酯、辛基三嗪酮、甲氧基肉桂酸辛酯、4-t-丁基-4′-甲氧基二苯甲酰基甲烷。特性赋予剂也可以是脱模剂、抗氧化剂、阻燃剂、填料、补强剂、紫外线防护剂、增塑剂、水运输剂/吸水剂或阳离子染色剂。
本发明也可提供由具有延长所获得的特性的聚合物产物制成的物体和产品。本文中所述的聚合物产物可用于制备纱线、织造织物、地毯和非织造织物。由本文中所述的聚合物产物制成的织物可用于多种最终应用,如用于制备消费产品;卫生产品;医疗产品;手术室产品,包括长袍、窗帘、无菌包装、鞋套、毛巾及相关物品。其他可由本文中所述的聚合物产物制成的织物制成的示例性产品包括运动服、袜子/短袜、橡胶垫圈和密封件、纤维填料、女性护理用品、尿布和失禁产品。
在随后的实施例和结果中,众多测试按照以下实验程序进行。
聚合物产物中抗菌剂的活性借助AATCC 147定性方法进行。测试利用葡萄球菌菌株ATCC 6538进行。样本下观察到生长且无抑制区域被认为是NO(亦即测试失败,无抗菌活性),而样本下没有观察到生长、有或没有抑制区域被认为是YES(测试通过,有抗菌活性)。
聚合物产物多个样本中香料的活性经专业调香师培训过的专家小组分析,通过将其与纯香料中所感觉到的香味进行比较,以区分香味的存在。如果大于70%或等于70%的专门小组人员能够识别出样品中的香料味道,则被认为是“是”(有效),少于70%的小组人员能识别出样品中的香料味道,则被认为是“否”(无效)。
聚合物产物中驱蚊活性由根据特定方法所测量的着陆蚊子数量的降低来测量。将一片聚合物产物置于盖有纱布的30x30x30cm蚊子笼顶上。将一个装满38±1℃的水的碗置于一片组织上。热的表面面积测定65cm2,起诱惑作用。蚊子笼含有100种埃及伊蚊雌蚊。1分钟和5分钟后对停在热组织上的蚊子进行计数。分别进行4次独立计数。使用多种测试样本进行相同程序。每个测试样本使用独立的蚊子群。5分钟后着陆数的降低为最终结果。着陆数降低量大于和等于30%则被认为“是”(具有预期效果),而小于30%的则被认为是“否”(没有预期效果)。
为了研究特性赋予剂的释放引入吐纳麝香香料成分。将产物洗涤、在20℃的环境温度下干燥,并在该温度下保持30分钟,测量其功效。在不同温度下研究本发明聚合物产物中香料物质的持续/受控释放。结果列于所附图1中。自图1可知,气味强度由香料小组按1-10的范围进行分析,其中1是最弱气味,10为最强气味。很明显,本发明聚合物产物中香料物质随温度进行持续/受控释放。
同时将含有储集体(熔点范围在35-65℃)的聚合物产物与作为抗菌成分的三氯生合并。将产物洗涤、在20℃的环境温度下干燥,此后将织物在该温度下保持30分钟,测量其功效。以24接触时间,依据AATCC 147进行抗菌分析,并测量抑制区域(mm)。研究聚合物产物中抗菌剂在不同温度下的持续/受控释放。结果见所附图2中。很明显自图2可知,本发明聚合物产物中抗菌剂随温度进行持续/受控释放。
经由以下非限制性实施例进一步说明本发明。
实施例1:延长保留所获得的特性的聚合物产物的制备
(a)用于制备聚合物产物的组合物:
在70℃通过将10g非极性有机储集体(表2中第2列中所指类型,例如石蜡)添加至4克HLB为15的非离子表面活性剂,Hydol 20和20g水中来制备石蜡乳液,使用超声发生器获得稳定乳液。将乳液添加至聚合物纺丝原液(表3中第3列所指,例如含有9%黄原酸盐形式的纤维素的粘胶纺丝原液)和6%碱中。
(b)能够延长保留所获得的特性的聚合物产物的制备
将实施例1(a)中所制备的组合物通过喷丝头纺至硫酸和硫酸铝/硫酸锌沉降槽内,按照标准纺丝程序加工以获得包含石蜡储集体的复合材料。所制备的聚合物产物列在表2(序列号1至20)。
(c)聚合物产物的处理:
将由实施例1(b)中所得的聚合物产物所制成的100g织物与1升含有特性赋予剂的溶液以1∶10的重量比在70℃下接触120分钟。接着利用2gpl标准洗涤剂在70℃下洗涤该织物30分钟,随后分别用热水和冷水洗涤15分钟。
实施例2:包含特性赋予剂的聚合物产物的传统制备方法
根据实施例1(b)和1(c)中所示的程序,进行聚合物产物的制备和聚合物产物的处理,以获得产物,不同的是聚合物纺丝原液在纺丝之前未与任何非极性有机储集体接触。照传统制备的聚合物产物列于表2(序列11至18),经处理的传统聚合物产物列于表1(序列22至29)。
实施例3:用于保留聚合物产物所获得的特性的测试
为了测试特性赋予剂所赋予的特性的保留情况,根据实施例1和实施例2所制备的聚合物产物样本,遵循AATCC程序,在AATCC标准洗涤剂存在下,于30至70℃温度范围下在洗衣机中洗涤至多20次。保留测试也通过处理如漂白、分散染料染色活性染料染色、预缩、树脂处理及固化表1第5列中所示聚合物产物样本而进行。确定这样处理后聚合物产物中特性的保留,并列于表1。
表1:根据实施例1(b)所制备的复合材料用特性赋予剂处理,及与传统聚合物产物的保留性进行比较进行的它们保留性研究
所有使用粘胶和纤维素的实施例均使用水作为溶胀剂,使用丙烯酸材料的实施例则使用苯甲醇作为溶胀剂。
用于上述纤维素实施例的离子液体则为乙基甲基咪唑鎓乙酸盐。
表2:由实施例1中方法所制备的多种聚合物产物
自上表可清楚,其中聚合物产物包含非极性有机储集体的本发明聚合物产物(样本号1至10)在洗涤或其他处理之后显示出特性的保留。本发明聚合物产物还可以用表2中所示的特性赋予剂重新加料。从质量和成本的长远角度考虑,特性/活性的延长保留是有利的。特性/活性的保留是由于石蜡储集体中特性赋予剂的保留。特性赋予剂的延长保留提供能够持久耐用并适用于制备高质量物体和产品的材料。特性赋予剂的延长保留也改善由聚合物产物制成的物体和产品的货架期。
虽然本文相当大的重点放在了优选方法的具体步骤上,但要认识到在不违背本发明原则的情况下,可做出很多步骤,而优选步骤中也可以进行多种改变。从本文所揭示内容可知,对于本领域技术人员而言,在本发明的优选步骤中的这些以及其他变化是显而易见的,借此可清楚地认识到上述问题的描述可以解释为说明本发明,而不是为限制本发明。
Claims (20)
1.一种将特性赋予剂加料至聚合物产物的方法,该方法包括:首先使聚合物纺丝原液或其前体与含有未包封非极性有机储集体的乳液接触,以形成包含纺丝原液和乳液的可纺组合物,然后通过模头纺织该组合物,以形成带有能够延长特性赋予剂保留的储集体的再生复合材料,最后使该复合材料或其产物与包含至少一种特性赋予剂和溶胀剂的配制剂在等于或大于储集体熔点的温度下在1到5巴的压力下接触至少15分钟。
2.根据权利要求1所述的方法,其中聚合物纺丝原液选自由粘胶纺丝原液、丙烯酸纺丝原液和纤维素纺丝原液组成的群组。
3.根据权利要求1或2所述的方法,其中有机储集体为熔点在10至120℃范围内的链烷烃、有机醇、有机脂肪酸或其酯、聚乙烯或其任何混合物。
4.根据权利要求1至3任一项所述的方法,其中复合材料与包含0.0001至15%特性赋予剂、0.01至99.999%溶胀剂及0.0001至15%表面活性剂的水性配制剂接触。
5.根据权利要求4所述的方法,其中表面活性剂选自由离子型表面活性剂、非离子表面活性剂、两性表面活性剂和聚合物表面活性剂组成的群组。
6.根据权利要求1至5任一项所述的方法,其中特性赋予剂为抗微生物剂、杀真菌剂、杀菌剂、灭藻剂、治疗剂、芳香族化合物、杀虫剂、杀螨剂、杀线虫剂、抗皱剂、柔软剂、抗氧化剂、阻燃剂、填料、补强剂、紫外防护剂、增塑剂、水运输剂/吸水剂、油溶性维生素、有机染料和着色剂、或其任何混合物。
7.根据权利要求1至6任一项所述的方法,其中溶胀剂选自由以下各物组成的群组:水、环己醇、正戊胺、正戊醇、1,5-二氨基戊烷、甘油、苯酚、苯甲醇、间甲苯胺、间甲酚、2-乙基苯酚、苄胺、苯胺、乙基苯胺、聚苯乙烯、酯/酚、乙腈、邻硝基苯酚、对硝基苯酚、二甲基甲酰胺、二甲亚砜、邻苯基苯酚、碳酸亚乙酯、碳酸亚丙酯、硝基甲烷、异戊醇、氢氧化钾、溶纤剂、甲基溶纤剂、异丙醇、丙醇和间甲酚。
8.根据权利要求1至7任一项所述的方法,其中复合材料与配制剂的重量比在1∶1至1∶500范围内。
9.根据权利要求8所述的方法,其中重量比在1∶5至1∶100范围内。
10.一种由权利要求1至9任一项所述的方法所制备的加料聚合物产物,其包含适用于保留一种或多种在非极性有机储集体中溶解度大于1%的特性赋予剂的未包封有机储集体。
11.根据权利要求10所述的聚合物产物,其中保留的特性赋予剂至多为储集体和所保留的特性赋予剂总重的60%。
12.根据权利要求10或11所述的聚合物产物,其中特性赋予剂为抗微生物剂、杀真菌剂、杀菌剂、灭藻剂、治疗剂、芳香化合物、杀虫剂、杀螨剂、杀线虫剂、抗皱剂、柔软剂、抗氧化剂、阻燃剂、填料、补强剂、紫外防护剂、增塑剂、水运输剂/吸水剂、油溶性维生素、有机染料和着色剂或其任何混合物。
13.根据权利要求10至12任一项所述的聚合物产物,其能够持续释放/受控释放特性赋予剂。
14.根据权利要求13所述的聚合物产物,其中特性赋予剂的释放受温度控制。
15.一种用于制备能够延长保留所获得的特性的聚合物产物的组合物,该组合物包含聚合物纺丝原液和熔点在10至120℃范围内的未包封非极性有机储集体。
16.根据权利要求15所述的组合物,其中聚合物纺丝原液为含有7-15%黄原酸盐形式的纤维素的粘胶纺丝原液。
18.根据权利要求15至17任一项所述的组合物,其中聚合物纺丝原液为选自丙烯酸聚合物、变性聚丙烯腈聚合物或其共混物的丙烯酸纺丝原液。
19.一种织造或非织造织物或任何聚合物材料,其由权利要求10至14任一项所述的聚合物产物制成。
20.一种物体或产品,其由权利要求19所述的织物制成。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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IN1946/MUM/2008 | 2008-09-12 | ||
IN1946MU2008 | 2008-09-12 | ||
PCT/IN2009/000501 WO2010041270A2 (en) | 2008-09-12 | 2009-09-11 | A process for charging a polymeric product with attribute imparting agent(s) |
Publications (1)
Publication Number | Publication Date |
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CN102232129A true CN102232129A (zh) | 2011-11-02 |
Family
ID=42101038
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Application Number | Title | Priority Date | Filing Date |
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CN2009801446318A Pending CN102232129A (zh) | 2008-09-12 | 2009-09-11 | 一种将特性赋予剂加料至聚合物产物的方法 |
Country Status (6)
Country | Link |
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US (1) | US20110166192A1 (zh) |
EP (1) | EP2326754A4 (zh) |
KR (1) | KR20110055711A (zh) |
CN (1) | CN102232129A (zh) |
BR (1) | BRPI1100969A2 (zh) |
WO (1) | WO2010041270A2 (zh) |
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US8772348B2 (en) * | 2009-12-03 | 2014-07-08 | University Of Florida Research Foundation, Inc. | Materials and methods for pest control |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
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GB599669A (en) * | 1940-04-02 | 1948-03-18 | Robert Wighton Moncrieff | Improvements in or relating to the production of artificial filaments, foils and like shaped articles |
US2081847A (en) * | 1934-08-13 | 1937-05-25 | North American Rayon Corp | Process of preparing cellulosic spinning solutions and soft-luster products thereof |
NL214053A (zh) * | 1956-02-01 | |||
NL272355A (zh) * | 1960-12-16 | |||
IT1038741B (it) * | 1975-06-06 | 1979-11-30 | Snam Progetti | Processo per l inglobamento di agenti sequestranti in strutture filamentose agenti seqesttanti inglobati cose ottenuti e loro applicazioni |
JP3165485B2 (ja) * | 1991-10-31 | 2001-05-14 | 宇部日東化成株式会社 | 消臭繊維およびその製造方法 |
US6172213B1 (en) | 1997-07-02 | 2001-01-09 | Genentech, Inc. | Anti-IgE antibodies and method of improving polypeptides |
US5968207A (en) * | 1998-02-20 | 1999-10-19 | Milliken & Company | Esterified triclosan derivatives as improved textile antimicrobial agents |
DE202005015408U1 (de) * | 2005-09-29 | 2006-02-09 | Optidee Produktions- Und Handels Gmbh | Textilie aus einem Mikrofasermaterial |
DE102006022009B3 (de) * | 2006-05-10 | 2007-12-06 | Thüringisches Institut für Textil- und Kunststoff-Forschung e.V. | Verfahren zur Herstellung cellulosischer Mehrkomponentenfasern |
DE102006046358B3 (de) * | 2006-09-28 | 2007-11-29 | Thüringisches Institut für Textil- und Kunststoff-Forschung e.V. | Verfahren zur Herstellung von funktionellen cellulosischen Formkörpern |
-
2009
- 2009-09-11 EP EP09818885A patent/EP2326754A4/en not_active Withdrawn
- 2009-09-11 WO PCT/IN2009/000501 patent/WO2010041270A2/en active Application Filing
- 2009-09-11 KR KR1020117007614A patent/KR20110055711A/ko not_active Application Discontinuation
- 2009-09-11 CN CN2009801446318A patent/CN102232129A/zh active Pending
-
2011
- 2011-03-10 US US13/045,106 patent/US20110166192A1/en not_active Abandoned
- 2011-03-14 BR BRPI1100969-1A patent/BRPI1100969A2/pt not_active IP Right Cessation
Also Published As
Publication number | Publication date |
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BRPI1100969A2 (pt) | 2012-06-19 |
US20110166192A1 (en) | 2011-07-07 |
WO2010041270A3 (en) | 2011-03-31 |
EP2326754A4 (en) | 2011-10-19 |
EP2326754A2 (en) | 2011-06-01 |
WO2010041270A2 (en) | 2010-04-15 |
KR20110055711A (ko) | 2011-05-25 |
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