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CN109971375B - 一种防水胶带基材和涂胶的方法 - Google Patents

一种防水胶带基材和涂胶的方法 Download PDF

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CN109971375B
CN109971375B CN201910301690.7A CN201910301690A CN109971375B CN 109971375 B CN109971375 B CN 109971375B CN 201910301690 A CN201910301690 A CN 201910301690A CN 109971375 B CN109971375 B CN 109971375B
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Abstract

本发明涉及医用胶带生产技术领域,具体涉及一种防水胶带基材和涂胶的方法。述防水胶带基材为双层结构,由防水层、基体层组成,本发明先得到透气性效果好的胶带基材;随后将胶带基材浸泡在Ti(SO4)2溶液中,负载二氧化钛在胶带基材中,不仅可以提高基材的抗菌性,还能保证后续的透气性,将负载二氧化钛的胶带基材表面进行等离子体处理,使基材表面形成大量反应基团,然后将双亲性聚合物溶液涂覆在其表面,亲水端会和基材表面进行结合,而疏水端在外面,制备得疏水膜。并且纳米二氧化钛颗粒的负载,高温加热后使形成的膜中形成均匀部分的孔径,该孔径保证防水性的同时还能具有优异的透气性。

Description

一种防水胶带基材和涂胶的方法
技术领域
本发明涉及医用胶带生产技术领域,具体涉及一种防水胶带基材和涂胶的方法。
背景技术
在外科手术后,用纱布包裹,其透气性好,但不具有防水性;后者大多采用具有透气孔的硅胶带,再在硅胶带的外面贴合一层防水透气膜,其优点是可以免去缝合的疼痛,具有防水性能,但其透气性能较差,这是由于一方面硅胶带的非孔区域仍占主要地位,整体上的透气性不足,另一方面,再贴合一层防水透气膜,不仅工序复杂,而且会在一定程度上阻碍透气性能,长期使用会影响伤口的愈合。同时现有的防水布料具有高防水性时,无法兼具透气度及抗污性,因此现有的防水透气兼具的医用胶带仍具有改善的必要。
发明内容
为了解决上述技术问题,本发明提供了一种防水胶带基材和涂胶的方法,使制得的胶带具有防水、透气及抗污性的功效。
为了解决上述技术问题,本发明采用的技术方案为:
所述防水胶带基材为双层结构,由防水层、基体层组成;
所述防水胶带基材的具体制备步骤为:
(1)将甲基丙烯酰胺、甲基丙烯酸十八酯、丙二醇甲醚醋酸酯混合后溶解于异丙醇中,加入引发剂,在氮气保护在升温至80℃进行反应,反应3~5h后停止搅拌加热,将反应得到的溶液用减压蒸馏去除溶剂,得聚合物溶液,然后加水,混合后置于超声波振荡器震荡腔内震荡,备用;
(2)将基材浸泡在0.3mol/L的Ti(SO4)2溶液中,用碱液调节pH为8,浸泡3~5h,浸泡后取出基材,并干燥;
(3)将干燥后的基材表面进行低温等离子体处理,处理时间为5~15s,处理功率为150~250W,得预处理后的基材;
(4)将预处理后的基材表面涂覆步骤(1)制备的聚合溶液,涂覆后置于烘箱中,置于真空干燥箱中,在80℃下干燥,干燥后得双层结构的防水胶带基材。
进一步,所述基体层是由棉纤维、麻纤维、腈纶纤维、涤纶纤维混纺编织而成。
进一步,所述甲基丙烯酰胺、甲基丙烯酸十八酯、丙二醇甲醚醋酸酯的摩尔比为1:1.2:1。
进一步所述步骤(4)所述的涂覆量为0.3~0.6g/cm2
所述涂胶步骤为:
(1)称取马铃薯淀粉,加入水中,搅拌混合均匀后加热至70~80℃进行糊化得混合物A,将透明质酸溶于MES酸性缓冲溶液中,不断搅拌使其完全溶解,然后加入乳化剂和过硫酸铵,得混合物B,继续升温至90~95℃,搅拌混合后向混合物A中分批加入混合物B和混合单体,将混合单体和混合物B滴加完毕后,进行搅拌反应,反应1~2h后降温,得液态胶;
(2)将液体胶按0.3~0.5g涂覆量涂覆在基体表面,涂覆后干燥,得防水胶带。
进一步,所述混合物B、混合单体和混合物A的质量比为1:1:5~10。
进一步,所述乳化剂为十二烷基磺酸钠;所述混合单体是由丙烯酸甲酯、丙烯酸乙酯和衣康酸混合而成。
与现有技术相比,本发明的有益效果为:
本发明基体层是由棉纤维、麻纤维、腈纶纤维、涤纶纤维混纺编织而成,可根据客户的需要进行调节,得到透气性效果好的胶带基材;随后将胶带基材浸泡在Ti(SO4)2溶液中,水解后形成二氧化钛负载在胶带基材中,不仅可以提高基材的抗菌性,还能保证后续的透气性。接着在负载二氧化钛的胶带基材表面进行等离子体处理,使得基材表面形成大量羟基等反应基团,然后将制备得到的聚合物溶液涂覆在其表面,由于聚合物溶液呈双亲性,亲水端会和基材表面进行结合,而疏水端在外面。从而使最终疏水防水膜。并且由于纳米二氧化钛颗粒的负载,高温加热后使形成的膜中形成均匀部分的孔径,该孔径保证防水性的同时还能具有优异的透气性。
具体实施方式
实施例1
(1)按摩尔比为1:1.2:1称取甲基丙烯酰胺、甲基丙烯酸十八酯、丙二醇甲醚醋酸酯混合后溶解于异丙醇中,加入引发剂,在氮气保护在升温至80℃进行反应,反应3h后停止搅拌加热,将反应得到的溶液用减压蒸馏去除溶剂,得聚合物溶液,然后加水,混合后置于超声波振荡器震荡腔内震荡,备用;
(2)基体层是由棉纤维、麻纤维、腈纶纤维、涤纶纤维混纺编织而成,将基材浸泡在0.3mol/L的Ti(SO4)2溶液中,用碱液调节pH为8,浸泡5h,浸泡后取出基材,并干燥;
(3)将干燥后的基材表面进行低温等离子体处理,处理时间为15s,处理功率为250W,得预处理后的基材;
(4)将预处理后的基材表面涂覆步骤(1)制备的聚合溶液,涂覆量为0.6g/cm2,涂覆后置于烘箱中,置于真空干燥箱中,在80℃下干燥,干燥后得双层结构的防水胶带基材。
(5)称取马铃薯淀粉,加入水中,搅拌混合均匀后加热至80℃进行糊化得混合物A,将透明质酸溶于MES酸性缓冲溶液中,不断搅拌使其完全溶解,然后加入十二烷基磺酸钠和过硫酸铵,得混合物B,继续升温至95℃,搅拌混合后向混合物A中分批加入混合物B和混合单体(由丙烯酸甲酯、丙烯酸乙酯和衣康酸混合而成),混合物B、混合单体和混合物A的质量比为1:1:10,将混合单体和混合物B滴加完毕后,进行搅拌反应,反应2h后降温,得液态胶;
(6)将液体胶按0.5g涂覆量涂覆在基体表面,涂覆后干燥,得防水胶带。
实施例2
(1)按摩尔比为1:1.2:1称取甲基丙烯酰胺、甲基丙烯酸十八酯、丙二醇甲醚醋酸酯混合后溶解于异丙醇中,加入引发剂,在氮气保护在升温至80℃进行反应,反应5h后停止搅拌加热,将反应得到的溶液用减压蒸馏去除溶剂,得聚合物溶液,然后加水,混合后置于超声波振荡器震荡腔内震荡,备用;
(2)基体层是由棉纤维、麻纤维、腈纶纤维、涤纶纤维混纺编织而成,将基材浸泡在0.3mol/L的Ti(SO4)2溶液中,用碱液调节pH为8,浸泡3h,浸泡后取出基材,并干燥;
(3)将干燥后的基材表面进行低温等离子体处理,处理时间为5s,处理功率为150W,得预处理后的基材;
(4)将预处理后的基材表面涂覆步骤(1)制备的聚合溶液,涂覆量为0.3~0.6g/cm2,涂覆后置于烘箱中,置于真空干燥箱中,在80℃下干燥,干燥后得双层结构的防水胶带基材。
(5)称取马铃薯淀粉,加入水中,搅拌混合均匀后加热至70℃进行糊化得混合物A,将透明质酸溶于MES酸性缓冲溶液中,不断搅拌使其完全溶解,然后加入十二烷基磺酸钠和过硫酸铵,得混合物B,继续升温至90℃,搅拌混合后向混合物A中分批加入混合物B和混合单体(由丙烯酸甲酯、丙烯酸乙酯和衣康酸混合而成),混合物B、混合单体和混合物A的质量比为1:1:5,将混合单体和混合物B滴加完毕后,进行搅拌反应,反应1h后降温,得液态胶;
(6)将液体胶按0.3g涂覆量涂覆在基体表面,涂覆后干燥,得防水胶带。
实施例3
(1)按摩尔比为1:1.2:1称取甲基丙烯酰胺、甲基丙烯酸十八酯、丙二醇甲醚醋酸酯混合后溶解于异丙醇中,加入引发剂,在氮气保护在升温至80℃进行反应,反应4h后停止搅拌加热,将反应得到的溶液用减压蒸馏去除溶剂,得聚合物溶液,然后加水,混合后置于超声波振荡器震荡腔内震荡,备用;
(2)基体层是由棉纤维、麻纤维、腈纶纤维、涤纶纤维混纺编织而成,将基材浸泡在0.3mol/L的Ti(SO4)2溶液中,用碱液调节pH为8,浸泡4h,浸泡后取出基材,并干燥;
(3)将干燥后的基材表面进行低温等离子体处理,处理时间为10s,处理功率为200W,得预处理后的基材;
(4)将预处理后的基材表面涂覆步骤(1)制备的聚合溶液,涂覆量为0.4g/cm2,涂覆后置于烘箱中,置于真空干燥箱中,在80℃下干燥,干燥后得双层结构的防水胶带基材。
(5)称取马铃薯淀粉,加入水中,搅拌混合均匀后加热至75℃进行糊化得混合物A,将透明质酸溶于MES酸性缓冲溶液中,不断搅拌使其完全溶解,然后加入十二烷基磺酸钠和过硫酸铵,得混合物B,继续升温至93℃,搅拌混合后向混合物A中分批加入混合物B和混合单体(由丙烯酸甲酯、丙烯酸乙酯和衣康酸混合而成),混合物B、混合单体和混合物A的质量比为1:1:7,将混合单体和混合物B滴加完毕后,进行搅拌反应,反应1.5h后降温,得液态胶;
(6)将液体胶按0.4g涂覆量涂覆在基体表面,涂覆后干燥,得防水胶带。
对比例1
对比例1与实施例1相比,主要区别在于:未将基材浸泡在Ti(SO4)2溶液中,其余制备步骤与实施例1相同。
对比例2
对比例2与实施例1相比,主要区别在于:未将基材表面进行低温等离子体处理,其余制备步骤与实施例1相同。
对比例3
对比例3与实施例1相比,主要区别在于:未在基材表面涂覆一层聚合物溶液,其余制备步骤与实施例1相同。
将上述实施例进行性能检测,检测结果如表1所示
表1:
Figure BDA0002026987730000051

Claims (5)

1.一种防水胶带基材,其特征在于:所述防水胶带基材由防水层、基体层双层结构组成;
所述防水胶带基材的具体制备步骤为:
(1)将甲基丙烯酰胺、甲基丙烯酸十八酯、丙二醇甲醚醋酸酯混合后溶解于异丙醇中,加入引发剂,在氮气保护在升温至80℃进行反应,反应3~5h后停止搅拌加热,将反应得到的溶液减压蒸馏去除溶剂,得聚合物溶液,然后加水,混合后置于超声波振荡器震荡腔内震荡,得双亲型聚合物溶液,备用;
(2)将基材浸泡在0.3mol/L 的Ti(SO4)2溶液中,用碱液调节pH为8,浸泡3~5h,浸泡后取出基材,并干燥;
所述基材是由棉纤维、麻纤维、腈纶纤维、涤纶纤维混纺编织而成;
(3)将干燥后的基材表面进行低温等离子体处理,处理时间为5~15s,处理功率为150~250W,得预处理后的基材;
(4)将预处理后的基材表面涂覆步骤(1)制备的得双亲型聚合物溶液,涂覆后置于烘箱中,置于真空干燥箱中,在80℃下干燥,干燥后得双层结构的防水胶带基材;
防水胶带基材的涂胶方法:称取马铃薯淀粉,加入水中,搅拌混合均匀后加热至70~80℃进行糊化得混合物A,将透明质酸溶于MES酸性缓冲溶液中,不断搅拌使其完全溶解,然后加入乳化剂和过硫酸铵,得混合物B,继续升温至90~95℃,搅拌混合后向混合物A中分批加入混合物B和混合单体,将混合单体和混合物B滴加完毕后,进行搅拌反应,反应1~2h后降温,得液态胶;
将液体胶按0.3~0.5g/cm2涂覆量涂覆在基体表面,涂覆后干燥,得防水胶带。
2.根据权利要求1所述防水胶带基材,其特征在于:所述甲基丙烯酰胺、甲基丙烯酸十八酯、丙二醇甲醚醋酸酯的摩尔比为1:1.2:1。
3.根据权利要求1所述防水胶带基材,其特征在于:所述步骤(4)所述的涂覆量为0.3~0.6g/cm2
4.根据权利要求1所述的防水胶带基材,其特征在于:所述混合物B、混合单体和混合物A的质量比为1:1:5~10。
5.根据权利要求1所述的防水胶带基材,其特征在于:所述乳化剂为十二烷基磺酸钠;所述混合单体是由丙烯酸甲酯、丙烯酸乙酯和衣康酸混合而成。
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