CN105463836A - 一种适于棉织物的新型抗菌整理剂及其制备方法 - Google Patents
一种适于棉织物的新型抗菌整理剂及其制备方法 Download PDFInfo
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Abstract
本发明公开了一种适于棉织物的新型抗菌整理剂,包括如下重量百分比的各组分:金银花乙醇提取物8-17份,蒲公英乙醇提取物6-15份,聚乙二醇10-20份,1-氨基-5-萘酚6-13份,十六烷基二甲基苄基氯化铵3-7份,邻羟基苯甲酸钠7-12份,丙烯酸丁酯2-8份,三异硬酯酸钛酸异丙酯9-13份,二癸基二甲基氯化铵2-6份,柠檬酸锌2.5-6,聚甲基丙烯酸15-20份。该整理剂较大的改善了棉织物的抗菌性能、提高其抗菌的持久性和长久性。
Description
技术领域
本发明属于整理剂领域,特别涉及一种适于棉织物的新型抗菌整理剂及其制备方法。
背景技术
近几年来,随着改革开放带来的不断红利,人们的生活水平和科技发展水平都取得了较大的提高,衣食住行中,衣即排在首位,人们对于衣服的要求自然也不断提高,特别是对于衣服的材质以及卫生状况等提出了更高的要求;而整理剂的出现即为满足人们这一要求提供了强有力的支撑。现如今,人们已经研究开发出了一些抗菌整理剂,这些现有的整理剂虽然能够起到一定的抗菌性能,但是其抗菌效果还未能完全满足人们所需,再加上抗菌的持久性和长效性较差,因而还有很大的改进空间。
发明内容
针对现有技术中存在的以上技术问题,本发明提供了一种适于棉织物的新型抗菌整理剂及其制备方法,以改善棉织物的抗菌性能、提高其抗菌的持久性和长久性。
技术方案:一种适于棉织物的新型抗菌整理剂,包括如下重量百分比的各组分:金银花乙醇提取物8-17份,蒲公英乙醇提取物6-15份,聚乙二醇10-20份,1-氨基-5-萘酚6-13份,十六烷基二甲基苄基氯化铵3-7份,邻羟基苯甲酸钠7-12份,丙烯酸丁酯2-8份,三异硬酯酸钛酸异丙酯9-13份,二癸基二甲基氯化铵2-6份,柠檬酸锌2.5-6,聚甲基丙烯酸15-20份。
进一步的,所述金银花乙醇提取物10-14份,蒲公英乙醇提取物8-12份,聚乙二醇12-15份,1-氨基-5-萘酚8-10份,十六烷基二甲基苄基氯化铵4-6份,邻羟基苯甲酸钠8-11份,丙烯酸丁酯3-6份,三异硬酯酸钛酸异丙酯10-13份,二癸基二甲基氯化铵3-5份,柠檬酸锌3-5,聚甲基丙烯酸16-18份。
进一步的,所述金银花乙醇提取物12份,蒲公英乙醇提取物10份,聚乙二醇13份,1-氨基-5-萘酚9份,十六烷基二甲基苄基氯化铵5份,邻羟基苯甲酸钠10份,丙烯酸丁酯5份,三异硬酯酸钛酸异丙酯12份,二癸基二甲基氯化铵4份,柠檬酸锌4,聚甲基丙烯酸17份。
一种适于棉织物的抗菌整理剂的制备方法,包含如下步骤:
S1:将金银花和蒲公英分别用乙醇制得金银花乙醇提取物和蒲公英乙醇提取物;
S2:取步骤S1中所得的金银花乙醇提取物8-17份和蒲公英乙醇提取物6-15份混合,并加入柠檬酸锌2.5-6份和聚甲基丙烯酸15-20份,常温下搅拌10-20min,得到混合液A;
S3:将聚乙二醇10-20份、丙烯酸丁酯2-8份、三异硬酯酸钛酸异丙酯9-13份和二癸基二甲基氯化铵2-6份加入反应器中,调整温度至30-40℃,在速度200-350r/min下搅拌反应8-15min;
S4:向步骤S3中按次序加入1-氨基-5-萘酚6-13份、十六烷基二甲基苄基氯化铵3-7份和邻羟基苯甲酸钠7-12份保持温度40-45℃下,搅拌反应5-10min,得到混合液B;
S5:将步骤S2中所得到的混合液A和步骤S4中得到的混合液B在温度50-65℃搅拌反应8-12min,经真空干燥后即可得到所述适于棉织物的抗菌整理剂。
进一步的,步骤S1中所述金银花和蒲公英的提取温度为75-80℃,提取时间为3.5-5h。
进一步的,步骤S2中搅拌的速度为250-350r/min。
进一步的,步骤S3中所述温度为36℃,所述速度为300r/min,搅拌反应的时间为12min。
进一步的,步骤S4中所述温度为42℃,所述搅拌反应的速度为150-200r/min,搅拌反应的时间为8min。
进一步的,步骤S4中所述温度为62℃,所述搅拌反应的速度为400-500r/min,搅拌反应的时间为9min。
有益效果:
本发明所述适于棉织物的抗菌整理剂制备方法,通过在制备整理剂的工艺中合理加入金银花乙醇提取物、蒲公英乙醇提取物、三异硬酯酸钛酸异丙酯和柠檬酸锌,有效的提高了制备所得的抗菌整理剂的抗菌效果,该制备方法简单;抗菌整理剂的抗菌效果对于金黄色葡萄球菌和大肠杆菌特别有效,同时其抗菌作用的持久性和长久性均得到较大提高,经过该整理剂整理后的棉织物手感和透气性也较好。该制备工艺简单、所需设备不复杂。
具体实施方式
实施例1
S1:将金银花和蒲公英分别用乙醇在温度75℃下提取3.5h制得金银花乙醇提取物和蒲公英乙醇提取物;
S2:取金银花乙醇提取物8份和蒲公英乙醇提取物6份混合,并加入柠檬酸锌2.5份和聚甲基丙烯酸15份,常温下以250r/min速度搅拌10min,得到混合液A;
S3:将聚乙二醇10份、丙烯酸丁酯2份、三异硬酯酸钛酸异丙酯9份和二癸基二甲基氯化铵2份加入反应器中,调整温度至30℃,在速度200r/min下搅拌反应8min;
S4:向步骤S3中按次序加入1-氨基-5-萘酚6份、十六烷基二甲基苄基氯化铵3份和邻羟基苯甲酸钠7份保持温度40℃,以150r/min的速度搅拌反应5min,得到混合液B;
S5:将步骤S2中所得到的混合液A和步骤S4中得到的混合液B在温度50℃下以400r/min的速度搅拌反应8min,经真空干燥后即可得到所述适于棉织物的抗菌整理剂。
对比例1
S1:将聚乙二醇10份、丙烯酸丁酯2份和二癸基二甲基氯化铵2份加入反应器中,调整温度至30℃,在速度200r/min下搅拌反应8min;
S2:向步骤S1中按次序加入1-氨基-5-萘酚6份、十六烷基二甲基苄基氯化铵3份和邻羟基苯甲酸钠7份保持温度40℃,以150r/min的速度搅拌反应5min,得到混合液;
S3:将聚甲基丙烯酸15份和步骤S2中得到的混合液在温度50℃下以400r/min的速度搅拌反应8min,经真空干燥后即可得到整理剂。
实施例2
S1:将金银花和蒲公英分别用乙醇在温度80℃下提取5h制得金银花乙醇提取物和蒲公英乙醇提取物;
S2:取金银花乙醇提取物17份和蒲公英乙醇提取物15份混合,并加入柠檬酸锌6份和聚甲基丙烯酸20份,常温下以350r/min速度搅拌20min,得到混合液A;
S3:将聚乙二醇20份、丙烯酸丁酯8份、三异硬酯酸钛酸异丙酯13份和二癸基二甲基氯化铵6份加入反应器中,调整温度至40℃,在速度350r/min下搅拌反应15min;
S4:向步骤S3中按次序加入1-氨基-5-萘酚13份、十六烷基二甲基苄基氯化铵7份和邻羟基苯甲酸钠12份保持温度45℃,以200r/min的速度搅拌反应10min,得到混合液B;
S5:将步骤S2中所得到的混合液A和步骤S4中得到的混合液B在温度65℃下以500r/min的速度搅拌反应12min,经真空干燥后即可得到所述适于棉织物的抗菌整理剂。
对比例2
S1:将聚乙二醇20份、丙烯酸丁酯8份、三异硬酯酸钛酸异丙酯13份和二癸基二甲基氯化铵6份加入反应器中,调整温度至40℃,在速度350r/min下搅拌反应15min;
S2:向步骤S1中按次序加入1-氨基-5-萘酚13份、十六烷基二甲基苄基氯化铵7份和邻羟基苯甲酸钠12份保持温度45℃,以200r/min的速度搅拌反应10min,得到混合液;
S3:将聚甲基丙烯酸20份和步骤S4中得到的混合液在温度65℃下以500r/min的速度搅拌反应12min,经真空干燥后即可得到整理剂。
实施例3
S1:将金银花和蒲公英分别用乙醇在温度75℃下提取3.5h制得金银花乙醇提取物和蒲公英乙醇提取物;
S2:取金银花乙醇提取物10份和蒲公英乙醇提取物8份混合,并加入柠檬酸锌3份和聚甲基丙烯酸16份,常温下以300r/min速度搅拌15min,得到混合液A;
S3:将聚乙二醇12份、丙烯酸丁酯3份、三异硬酯酸钛酸异丙酯10份和二癸基二甲基氯化铵3份加入反应器中,调整温度至30℃,在速度250r/min下搅拌反应8min;
S4:向步骤S3中按次序加入1-氨基-5-萘酚8份、十六烷基二甲基苄基氯化铵4份和邻羟基苯甲酸钠8份保持温度40℃,以150r/min的速度搅拌反应5min,得到混合液B;
S5:将步骤S2中所得到的混合液A和步骤S4中得到的混合液B在温度50℃下以400r/min的速度搅拌反应8min,经真空干燥后即可得到所述适于棉织物的抗菌整理剂。
实施例4
S1:将金银花和蒲公英分别用乙醇在温度80℃下提取3.5h制得金银花乙醇提取物和蒲公英乙醇提取物;
S2:取金银花乙醇提取物14份和蒲公英乙醇提取物12份混合,并加入柠檬酸锌5份和聚甲基丙烯酸18份,常温下以250r/min速度搅拌10min,得到混合液A;
S3:将聚乙二醇15份、丙烯酸丁酯6份、三异硬酯酸钛酸异丙酯13份和二癸基二甲基氯化铵5份加入反应器中,调整温度至40℃,在速度350r/min下搅拌反应15min;
S4:向步骤S3中按次序加入1-氨基-5-萘酚10份、十六烷基二甲基苄基氯化铵6份和邻羟基苯甲酸钠11份保持温度45℃,以200r/min的速度搅拌反应10min,得到混合液B;
S5:将步骤S2中所得到的混合液A和步骤S4中得到的混合液B在温度60℃下以500r/min的速度搅拌反应12min,经真空干燥后即可得到所述适于棉织物的抗菌整理剂。
实施例5
S1:将金银花和蒲公英分别用乙醇在温度78℃下提取4h制得金银花乙醇提取物和蒲公英乙醇提取物;
S2:取金银花乙醇提取物12份和蒲公英乙醇提取物10份混合,并加入柠檬酸锌4份和聚甲基丙烯酸17份,常温下以300r/min速度搅拌15min,得到混合液A;
S3:将聚乙二醇13份、丙烯酸丁酯5份、三异硬酯酸钛酸异丙酯12份和二癸基二甲基氯化铵4份加入反应器中,调整温度至36℃,在速度300r/min下搅拌反应12min;
S4:向步骤S3中按次序加入1-氨基-5-萘酚5份、十六烷基二甲基苄基氯化铵6份和邻羟基苯甲酸钠5份保持温度42℃,以180r/min的速度搅拌反应8min,得到混合液B;
S5:将步骤S2中所得到的混合液A和步骤S4中得到的混合液B在温度62℃下以450r/min的速度搅拌反应9min,经真空干燥后即可得到所述适于棉织物的抗菌整理剂。
取纯棉织物,将以上各个实施例和对比例的整理剂分别整理纯棉织物,二浸二轧,轧余率为70%,在温度为80℃下烘干。测定纯棉织物对大肠杆菌和金黄色葡萄球菌的抑菌率,具体抑菌率如下:
实验 | 大肠杆菌抑菌率(%) | 金黄色葡萄球菌抑菌率(%) |
实施例1 | 75 | 78 |
对比例1 | 48 | 57 |
实施例2 | 81 | 77 |
对比例2 | 50 | 53 |
实施例3 | 82 | 81 |
实施例4 | 87 | 83 |
实施例5 | 86 | 88 |
以实施例5所制备的整理剂为例,经检测,30次洗涤之后抑菌率依然保持在较高水平,大肠杆菌抑菌率为70%,金黄色葡萄球菌抑菌率为69%。
Claims (9)
1.一种适于棉织物的新型抗菌整理剂,其特征在于,包括如下重量百分比的各组分:金银花乙醇提取物8-17份,蒲公英乙醇提取物6-15份,聚乙二醇10-20份,1-氨基-5-萘酚6-13份,十六烷基二甲基苄基氯化铵3-7份,邻羟基苯甲酸钠7-12份,丙烯酸丁酯2-8份,三异硬酯酸钛酸异丙酯9-13份,二癸基二甲基氯化铵2-6份,柠檬酸锌2.5-6份,聚甲基丙烯酸15-20份。
2.根据权利要求1所述的一种适于棉织物的新型抗菌整理剂,其特征在于,所述金银花乙醇提取物10-14份,蒲公英乙醇提取物8-12份,聚乙二醇12-15份,1-氨基-5-萘酚8-10份,十六烷基二甲基苄基氯化铵4-6份,邻羟基苯甲酸钠8-11份,丙烯酸丁酯3-6份,三异硬酯酸钛酸异丙酯10-13份,二癸基二甲基氯化铵3-5份,柠檬酸锌3-5份,聚甲基丙烯酸16-18份。
3.根据权利要求2所述的一种适于棉织物的新型抗菌整理剂,其特征在于,所述金银花乙醇提取物12份,蒲公英乙醇提取物10份,聚乙二醇13份,1-氨基-5-萘酚9份,十六烷基二甲基苄基氯化铵5份,邻羟基苯甲酸钠10份,丙烯酸丁酯5份,三异硬酯酸钛酸异丙酯12份,二癸基二甲基氯化铵4份,柠檬酸锌4份,聚甲基丙烯酸17份。
4.一种适于棉织物的新型抗菌整理剂的制备方法,其特征在于,包含如下步骤:
S1:将金银花和蒲公英分别用乙醇制得金银花乙醇提取物和蒲公英乙醇提取物;
S2:取步骤S1中所得的金银花乙醇提取物8-17份和蒲公英乙醇提取物6-15份混合,并加入柠檬酸锌2.5-6份和聚甲基丙烯酸15-20份,常温下搅拌10-20min,得到混合液A;
S3:将聚乙二醇10-20份、丙烯酸丁酯2-8份、三异硬酯酸钛酸异丙酯9-13份和二癸基二甲基氯化铵2-6份加入反应器中,调整温度至30-40℃,在速度200-350r/min下搅拌反应8-15min;
S4:向步骤S3中按次序加入1-氨基-5-萘酚6-13份、十六烷基二甲基苄基氯化铵3-7份和邻羟基苯甲酸钠7-12份保持温度40-45℃下,搅拌反应5-10min,得到混合液B;
S5:将步骤S2中所得到的混合液A和步骤S4中得到的混合液B在温度50-65℃搅拌反应8-12min,经真空干燥后即可得到所述适于棉织物的抗菌整理剂。
5.根据权利要求4所述的一种适于棉织物的新型抗菌整理剂的制备方法,其特征在于,步骤S1中所述金银花和蒲公英的提取温度为75-80℃,提取时间为3.5-5h。
6.根据权利要求4所述的一种适于棉织物的新型抗菌整理剂的制备方法,其特征在于,步骤S2中搅拌的速度为250-350r/min。
7.根据权利要求4所述的一种适于棉织物的新型抗菌整理剂的制备方法,其特征在于,步骤S3中所述温度为36℃,所述速度为300r/min,搅拌反应的时间为12min。
8.根据权利要求4所述的一种适于棉织物的新型抗菌整理剂的制备方法,其特征在于,步骤S4中所述温度为42℃,所述搅拌反应的速度为150-200r/min,搅拌反应的时间为8min。
9.根据权利要求4所述的一种适于棉织物的新型抗菌整理剂的制备方法,其特征在于,步骤S4中所述温度为62℃,所述搅拌反应的速度为400-500r/min,搅拌反应的时间为9min。
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