CN113005769A - 一种抗菌面料的制备方法及其面料 - Google Patents

一种抗菌面料的制备方法及其面料 Download PDF

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CN113005769A
CN113005769A CN202110221825.6A CN202110221825A CN113005769A CN 113005769 A CN113005769 A CN 113005769A CN 202110221825 A CN202110221825 A CN 202110221825A CN 113005769 A CN113005769 A CN 113005769A
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antibacterial
antibacterial fabric
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CN113005769B (zh
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刘斌
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Hangzhou Jinfeng Silk Co ltd
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Abstract

本申请涉及纺织技术领域,具体公开了一种抗菌面料的制备方法及其面料,该抗菌面料的制备方法包括以下步骤:将纤维经过第一整理剂浸渍,浸渍后进行烘干,并将纤维进行编织,得到编织后的坯布,后经过第二整理剂浸渍,后进行烘干;将烘干后的坯布浸渍于抗菌剂中浸渍,浸渍后进行烘干;后进行染色、清洗、烘干后得到该抗菌面料;纤维由木棉纤维、莫代尔纤维和涤纶纤维组成;第一整理剂包括以下重量份的原料:乙二醛1‑2份、乙二醇0.5‑1份、氯化钙2‑3份、渗透剂2‑5份、增强剂1‑1.5份、水90‑100份;抗菌剂由以下重量份的组分组成:季铵盐1‑2份、水溶性壳聚糖3‑4份、金银花提取物0.5‑1份、薄荷醇0.5‑1份、水90‑110份;由该制备方法得到的抗菌面料具有抗皱性好的优点。

Description

一种抗菌面料的制备方法及其面料
技术领域
本申请涉及纺织技术领域,尤其涉及一种抗菌面料的制备方法及其面料。
背景技术
抗菌面料是指经过特殊处理的面料,这种面料经过抗菌处理和混合抗菌纤维纺织而成, 由抗菌面料制成的织物能够让细菌失去活性,从而保护人体健康。
公开号为CN103255538A,公开日2013年08月21日公开的一种抗菌面料,由下述重量份纤维混纺织造成混纺面料:30-50份Lyocell纤维、10-30份涤纶长丝纤维、10-30份莫代尔纤维、10-30份亚麻纤维,混纺面料后在抗菌整理剂中浸渍得到抗菌面料,抗菌整理剂由以 下重量份的组分组成:甲壳素30-50份、白芥末油10-30份、壳聚糖10-30份。
针对上述中的相关技术,上述制备的抗菌面料虽然具有抗菌效果,但未经过抗皱处理, 导致抗菌面料的抗皱性能较差。
发明内容
为了增强抗菌面料的抗皱性能,本申请提供了一种抗菌面料的制备方法及其面料。
第一方面,本申请提供一种抗菌面料的制备方法,采用如下的技术方案:
一种抗菌面料的制备方法,包括以下步骤:
S1:将纤维经过第一整理剂浸渍,浸渍后进行烘干,并将纤维进行编织,得到编织后的坯布;
S2:将编织后的坯布经过第二整理剂浸渍,浸渍后进行烘干;
S3:将步骤S2中烘干后的坯布浸渍于抗菌剂中浸渍,浸渍后进行烘干;
S4:将步骤S3中烘干后的坯布进行清洗、烘干后得到该抗菌面料;
所述纤维纤维由木棉纤维、莫代尔纤维和涤纶纤维组成;
所述第一整理剂包括以下重量份的原料:
乙二醛1-2份;
乙二醇0.5-1份;
氯化钙2-3份;
渗透剂2-5份;
增强剂1-1.5份;
水90-100份;
所述抗菌剂由以下重量份的组分组成:
季铵盐1-2份;
水溶性壳聚糖3-4份;
金银花提取物0.5-1份;
薄荷醇0.5-1份;
水90-110份。
通过采用上述技术方案,采用木棉纤维、莫代尔纤维、涤纶纤维作为编织纤维,首先 经过第一整理剂进行浸渍,第一整理剂中的乙二醛、乙二醇共同配合增强纤维的抗皱性能和 柔软性;第一整理剂中的氯化钙与乙二醛、乙二醇作用,快速增强纤维的抗皱性能;渗透剂 与乙二醛、乙二醇共同配合,将乙二醇、乙二醛渗透到纤维内部,从而增强纤维的抗皱性能 和柔软性;增强剂与纤维配合,使得由纤维编织后的坯布具有较好的韧性和柔软性;后采用 第二整理剂浸渍坯布,与第一整理剂共同作用,使得坯布获得长久的抗皱性能;后在抗菌剂 中浸渍,去除坯布在前期浸渍过程中聚积的细菌等物质,起到抗菌效果;抗菌剂采用季铵盐、 水溶性壳聚糖、金银花提取物与薄荷醇组合,起到较好的杀菌效果;综上所述,通过采用柔 软性较好的木棉纤维,抗皱性能较好的莫代尔纤维、涤纶纤维,通过第一整理剂中乙二醇、 乙二醛配合,增强抗菌面料的抗皱性能,后经过第二整理剂浸渍,使得抗菌面料获得长久的 抗皱性能。
优选的,所述渗透剂包括脂肪醇聚氧乙烯醚、磺化琥珀酸二辛酯钠盐中的至少一种。
通过采取上述技术方案,渗透剂采用脂肪醇聚氧乙烯醚、磺化琥珀酸二辛酯钠盐中一 种或者两种,有效地帮助乙二醛、乙二醇等主要组分渗透入纤维中,从而赋予纤维较好的抗 皱性和柔软性,使得由该纤维制备得到的抗菌面料具有较好的抗皱性能。
优选的,所述增强剂由聚乙烯和膨润土组成。
通过采取上述技术方案,增强剂中的聚乙烯通过与乙二醛、乙二醇配合共同维持抗菌 面料的抗皱性,膨润土与聚乙烯共同配合,增强抗菌面料的平整性和韧性。
优选的,所述第一整理剂的原料中还包括重量份数为0.5-1份的苦丁茶提取物。
通过采用上述技术方案,苦丁茶提取物在加入纤维后,可以增强纤维的抗紫外线性能, 对抗菌面料进行保护,防止抗菌面料由于紫外线照射发生变色、寿命减少等问题,进一步保 护抗菌面料,延长抗菌面料的寿命。
优选的,所述第二整理剂包括以下重量份的原料:
柠檬酸1-2份;
碳羟基聚硅氧烷1-1.5份;
丝素蛋白0.5-0.8份;
水80-100份。
通过采用上述技术方案,柠檬酸、碳羟基聚硅氧烷与纤维共同作用,增强抗菌面料的 柔软性,并与第一整理剂中的乙二醛、乙二醇共同配合,使得抗菌面料获得较为长久的抗皱 性能;丝素蛋白在加入第二整理剂后,丝素蛋白与坯布具有较好的相容性,具有较好的弹性 粘结性能,使得纤维之间的粘结能力更强,进而增强抗菌面料的韧性,抗菌面料不易形变, 可以获得较好的抗皱性能。
优选的,所述第二整理剂中还包括重量份数为0.1-0.2份的杏仁粉。
通过采用上述技术方案,杏仁粉与丝素蛋白混合后,有助于增强丝素蛋白的粘结性能, 从而进而增强抗菌面料的柔韧性。
优选的,所述木棉纤维、莫代尔纤维以及涤纶纤维的重量比为1:2:(1-2)。
通过采取上述技术方案,优选木棉纤维、莫代尔纤维以及涤纶纤维的重量比后进行混 纺编织,从而使得获得的抗菌面料具有较好的抗皱性和柔软性。
优选的,所述步骤S1中的浸渍时间为3-5h、浸渍温度为70-90℃。
通过采用上述技术方案,控制纤维浸渍于第一整理剂中的时间和温度,使得纤维充分 与第一整理剂混合,并通过渗透剂将乙二醛、乙二醇等浸入纤维中,从而使得原料纤维具有 较好的抗皱性和柔韧性。
优选的,所述步骤S2中的浸渍时间2-3h,浸渍温度为50-60℃。
通过采用上述技术方案,控制坯布浸渍于第二整理剂中的时间和温度,使得第二整理 剂中的柠檬酸和碳羟基聚硅氧烷充分与坯布结合,增强混合的均匀性,使得抗菌面料具有较 好的抗皱性和柔韧性。
第二方面,本申请提供一种抗菌面料,采用如下的技术方案:
一种抗菌面料,通过上述制备方法制得。
通过采用上述技术方案,得到的抗菌面料具有较好的抑菌能力和抗皱性能。
综上所述,本申请具有以下有益效果:
1.由于本申请采用木棉纤维、莫代尔纤维、涤纶纤维作为编织纤维,第一整理剂中的乙二醛 和乙二醇共同作用,并在渗透剂的作用下,进入纤维中,赋予制备后的抗菌面料较好的抗皱 性能和柔韧性;抗菌剂中的水溶性壳聚糖,以及天然物质金银花提取物和薄荷醇起到较好的 杀菌作用。
2.在本申请中,优选采用脂肪醇聚氧乙烯醚、磺化琥珀酸二辛酯钠盐中的至少一种作 为渗透剂,有效地帮助乙二醇、乙二醛渗透入纤维中,增强纤维的抗皱性;优选聚乙烯和膨 润土作为增强剂,并与乙二醛配合,维持抗菌面料的抗皱性;后通过在第一整理剂中加入苦 丁茶提取物赋予抗菌面料较好的抗紫外线性能;第二整理剂中加入柠檬酸、碳羟基聚硅氧烷 并与坯布作用,增强抗菌面料的柔韧性,同时丝素蛋白和杏仁粉配合,增强丝素蛋白的粘结 性能,使得纤维之间的粘结能力更强,增强抗菌面料的韧性。
3.本申请中,控制纤维浸渍于第一整理剂中的时间,控制编织成的坯布浸渍于第二整 理剂中的时间和温度,从而充分浸渍均匀,赋予抗菌面料更好地抗皱性和柔韧性。
具体实施方式
以下对本申请作进一步详细说明。
各实施例中的组分及生产厂家如表1所示。
表1组分及生产厂家
组分 型号/规格 生产厂家
木棉纤维 AR-6 山东省奥绒服装有限公司
莫代尔纤维 05 山东中纤纺织科技有限公司
涤纶纤维 hy0081 山东久绵纺织品有限公司
乙二醛 107-22-2 山东嘉润化工有限公司
乙二醇 58966 上海富畦工贸有限公司
氯化钙 10043-52-4 南通润丰石油化工有限公司
碳羟基聚硅氧烷 IOTA 2170 安徽艾约塔硅油有限公司
脂肪醇聚氧乙烯醚 AEO9 济南杰维化工科技有限公司
丝素蛋白 QADB-1 西安全奥生物科技有限公司
苦丁茶提取物 XCSW20201105 宁夏香草生物技术有限公司
水溶性壳聚糖 4562134 安徽中弘生物工程有限公司
季铵盐 LA-D12 山东力昂新材料科技有限公司
金银花提取物 fdqwrq 江苏采薇生物科技有限公司
薄荷醇 ft11 山东丰泰生物科技有限公司
磺化琥珀酸二辛酯钠盐 kds54564 康迪斯化工(湖北)有限公司
聚乙烯 MB9500 上海超旋化工科技有限公司
膨润土 1302-78-9 灵寿县圣亚矿产品有限公司
柠檬酸 102 华骅市天信化工有限公司
杏仁粉 ety038 西安恩肽元生物科技有限公司
渗透剂 JFC-4 上海链集化工有限公司
实施例1:
一种抗菌面料,所包括的具体组分以及重量如表2所示,由以下步骤制得:
S1:将乙二醇、乙二醛、氯化钙、渗透剂JFC-4、增强剂膨润土、水混合搅拌,搅拌速度为600r/min, 搅拌均匀后得到第一整理剂;将柠檬酸、碳羟基聚硅氧烷、水混合搅拌,搅拌速度为800r/min, 搅拌均匀后得到第二整理剂;将季铵盐、水溶性壳聚糖、金银花提取物、薄荷醇混合搅拌, 搅拌速度为600r/min,搅拌均匀得到抗菌剂;
S2:将纤维(木棉纤维、莫代尔纤维以及涤纶纤维)经过第一整理剂浸渍,浸渍时间为3h,浸 渍温度为90℃,浸渍后采用烘干箱烘干,烘干温度为70℃,烘干后将三种纤维进行加捻,整 经和混纺后得到编织后的坯布;(上述的加捻、整经和混纺均为本行业的通用方法,为本领域 普通技术人员所熟知)
S3:将编织后的坯布经过第二整理剂浸渍浸渍时间为2h,浸渍温度为60℃,浸渍后采用烘干 箱进行烘干,烘干温度为65℃;
S4:将步骤S3中烘干后的坯布浸渍于抗菌剂中浸渍,浸渍时间30min,浸渍后进行烘干,烘 干温度为65℃;
S5:将步骤S4中烘干后的坯布用水冲洗10min,并烘干,烘干温度为45℃,烘干后得到该抗 菌面料。
实施例2-3:一种抗菌面料,与实施例1的区别在于,具体组分及重量不同,所包括的 具体组分及重量如表2所示。
实施例4-5:一种抗菌面料,与实施例1的区别在于,渗透剂组分和重量比不同,所包 括的具体组分及重量如表2所示。
实施例6-7:一种抗菌面料,与实施例1的区别在于,增强剂的组分及重量不同,所包 括的具体组分及重量如表2所示。
实施例8-9:一种抗菌面料,与实施例1的区别在于,第一整理剂中还含有苦丁茶提取 物,所包括的具体组分及重量如表2所示。
表2实施例1-9的具体组分及重量
Figure BDA0002955243620000051
Figure BDA0002955243620000061
实施例10-11:一种抗菌面料,与实施例1的区别在于,第二整理剂的具体组分及重量不同, 所包括的具体组分及重量如表3所示。
实施例12-13:一种抗菌面料,与实施例1的区别在于,在步骤S1制备第二整理剂中加 入杏仁粉,所包括的具体组分及重量如表3所示。
实施例14-15:一种抗菌面料,与实施例1的区别在于,纤维的组成不同,所包括的具 体组分及重量如表3所示。
实施例16-17:一种抗菌面料,与实施例1的区别在于,各组分及重量不同,所包括的 具体组分及重量如表3所示。
表3实施例10-17的具体组分及重量
Figure BDA0002955243620000062
Figure BDA0002955243620000071
实施例18:一种抗菌面料,与实施例1的区别在于,在步骤S2中浸渍于第一整理剂中的浸渍 时间5h,浸渍温度70℃。
实施例19:一种抗菌面料,与实施例1的区别在于,在步骤S3中浸渍于第二整理剂中 的浸渍时间3h,浸渍温度50℃。
对比例
对比例1:一种面料,与实施例1的区别在于,用等量的水替代第一整理剂中的乙二醛。
对比例2:一种面料,与实施例1的区别在于,用等量的水替代第一整理剂中的乙二醇。
对比例3:一种面料,与实施例1的区别在于,用等量的水替代第一整理剂中的乙二醛 和乙二醇。
对比例4:一种面料,与实施例1的区别在于,用等量的水替代抗菌剂中的金银花提取 物。
对比例5:一种面料,与实施例1的区别在于,用等量的水替代抗菌剂中的薄荷醇。
对比例6:一种面料,与实施例1的区别在于,用等量的水替代抗菌剂中的薄荷醇和金 银花提取物。
对比例7:一种面料,称取40kgLyocell纤维、20kg涤纶长丝纤维、20kg莫代尔纤维、20kg亚麻纤维,分别开松预处理,在梳棉机上梳理成Lyocell纤维生条、涤纶长丝纤维生条、莫代尔纤维生条、亚麻纤维生条;在并条机上并合,制成熟条;在粗纱机上进行牵伸和加捻,最后在细纱机上进一步牵伸加捻,制成混纺纱;再将混纺纱采用大圆机纬编织造方法进行织 造,最终制得本发明的抗菌面料(60支)。上述的混纺纱及面料的制备工艺均为本行业的通 用方法,为本领域普通技术人员所熟知。取混纺面料,进一步进行抗菌后整理,具体步骤为: 抗菌整理剂的配置:将甲壳素30kg、白芥末油30kg、壳聚糖10kg,搅拌混合均匀,制得抗菌整理剂;
浸渍:将抗菌整理剂加入水中,用稀盐酸调节pH值到6.5,得抗菌整理液,控制抗菌整理液 中抗菌整理剂的含量为0.15%;再将混纺面料25℃下在抗菌整理液中浸渍30分钟,混纺面料 与抗菌整理液的重量体积比为0.2kg/L。
脱水;烘干:在100℃温度下将织物烘干,即可制得该抗菌面料。
Lyocell纤维来自山东久绵纺织品有限公司,型号zxw018;涤纶长丝纤维来自山东久绵 纺织品有限公司,型号hy0081;莫代尔纤维来自山东中纤纺织科技有限公司,型号05;亚麻 纤维来自东莞市精盈纤维制品有限公司,货号JYYM001;甲壳素来自河北科隆多生物科技有 限公司,货号fg-00;白芥末油来自众信居(天津)食品制造有限公司;壳聚糖来自西格玛奥德 里奇(上海)贸易有限公司,型号为448877;稀盐酸来自扬州市华富化工有限公司,浓度10%。
检测方法
实验一:抗菌性能实验 实验样品:将实施例1-19以及对比例1-7得到的抗菌面料制成直径为4.8cm的圆形试片,并 将由实施例1-19制成的圆形试片分别命名为实验样品1-19,将对比例1-7制成的圆形试片分 别命名为对比样品1-7。
实验仪器:培养基(营养肉汤/琼脂培养基;胰蛋白胨大豆肉汤/琼脂;脑心浸出液肉 汤/琼脂);培养箱;接种环;酒精灯;水浴锅;灭菌移液管;无菌培养皿(规格100mm×15mm); 立体显微镜(40x镜像)。
实验方法:根据AATCC 100-2012的《抗菌纺织品的评价方法》中的检测方法对实验样品1-19以及对比样品1-7的抗菌能力实验。
实验结果:实验样品1-19以及对比样品1-7的抗菌性能实验结果如表4所示。
实验二:抗皱性能实验 实验样品:将实施例1-19以及对比例1-7制成40mm×15mm的长方形试样,并将由实施例 1-1制备的试样分别命名为实验样品1-19,将对比例1-7制备的试样分别命名为对比样品1-7。
实验方法:根据GB/T3819-1997的《纺织品织物折痕回复性的测定回复角法》中的水平法对实验样品1-19以及对比样品1-7在120s时的经向缓弹回复角和纬向缓弹回复角进行 检测,并将两者结果进行相加得到最终的回复角,回复角越大,抗皱性能越好,实验仪器采 用该国标中的压力负荷装置。
实验结果:实验样品1-19以及对比样品1-7的抗皱性能实验结果如表4所示。
实验三:断裂强力实验 实验样品:采用实施例1-19以及对比例1-7制成的尺寸为200mm×50mm的试样,并将由实 施例1-19得到的试样分别命名为实验样品1-19,将由对比例1-7得到的试样分别命名为对比 样品1-7,实验样品1-19以及对比样品1-7均有5个。
实验仪器:等速拉伸试验仪(品牌为美斯特试验机有限公司;型号为WAL)。
实验方法:根据国标GB/T 3923.1-1997的《纺织品织物拉伸性能断裂强力和断裂伸 长率的测定条样法》中的检测方法对实验样品1-19以及对比样品1-7进行断裂强力实验。
实验结果:实验样品1-19以及对比样品1-7的断裂强力实验结果如表4所示。
实验四:柔软度实验 实验样品:采用实施例1-19以及对比例1-7应用于衬衫上,并将由实施例1-16得到的衬衫分 别命名为实验样品1-19,将由对比例1-7得到的衬衫分别命名为对比样品1-7,实验样品1-19 以及对比样品1-7均有5个。
实验对象:招募同一地区的25-35岁的健康中国人260名,平均分成26个实验组,且分别对应实验样品1-19和对比样品1-7。
评价方法:实验对象分别穿着实验样品1-19以及对比样品1-7,两天后,对实验样品 1-19以及对比样品1-7进行打分;打分标准如下:
柔软度打分:1-10分,柔软度越高分值越高,手感越硬分值越低;打分后,取每个实验组的 打分平均值作为最终的使用感评价分数。
实验结果:实验样品1-19以及对比样品1-7的柔软度实验结果如表4所示。
表4实验样品1-19以及对比样品1-7的抗菌性、抗皱性、断裂强力以及柔软度实验结 果
Figure BDA0002955243620000091
Figure BDA0002955243620000101
由表4的实验数据可知,实验样品1-19的抗菌率均超过90%,回复角为269.8-283.6°回复角 较大,说明实验样品1-19具有较好的抗菌性和抗皱性;另外实验样品1-19的断裂强力为 423.4-436.1N,说明实验样品1-19的柔韧性较好;而对比样品1-7的回复角较小、断裂强力 较小,说明相比于实验样品1-19,对比样品1-7的抗皱性能较差,柔韧性也较差。
对比实验样品1和对比样品1-3可知,当第一整理剂中含有乙二醇或者乙二醛时,回 复角有一定的增加,说明抗皱性能有所增强,而当两者均含有时,抗皱性能增加幅度较多, 说明乙二醇和乙二醛复配后,更有助于增强抗菌面料的抗皱性能;对比实验样品1和对比样 品4-6可知,当抗菌剂中含有金银花或者薄荷醇时,抗菌性能有一定的提高,说明金银花和 薄荷醇均可增强面料的抗菌性能,而当两者均含有时,抗菌性能增加程度最大,说明金银花 和薄荷醇复配后,更有助于增强抗菌面料的抗菌性能;对比实验样品1和对比样品7可知, 经过第一整理剂、第二整理剂以及抗菌剂浸渍后的面料具有较好抗菌性、抗皱性以及柔韧性。
对比实验样品1和实验样品4-5可知,渗透剂采用脂肪醇聚氧乙烯醚、磺化琥珀酸二 辛酯钠盐后,抗菌面料的抗菌性、抗皱性均有一定提高,说明脂肪醇聚氧乙烯醚、磺化琥珀 酸二辛酯钠盐有助于增强抗菌面料的抗菌性、抗皱性,脂肪准聚氧乙烯醚、磺化琥珀酸二辛 酯钠盐具有较好的渗透作用,将乙二醇和乙二醛快速并充分渗透入纤维中,从而使得由该纤 维织成抗菌面料的抗菌性和抗皱性得到提高;对比实验样品1和实验样品6-7可知,增强剂 采用聚乙烯和膨润土后,抗菌面料的抗皱性能和断裂强力有了一定的提高,说明聚乙烯和膨 润土加入第一整理剂后,可以增强抗菌面料的抗皱性能和断裂强力;聚乙烯韧性较强,膨润 土具有较好的粘结力和强度,两者配合后,有效地和面料作用,赋予面料优异的韧性,从而 增强抗菌面料的抗皱性能;对比实验样品1和实验样品8-9可知,苦丁茶提取物加入后可以 增强抗菌面料的抗菌性和断裂强力,苦丁茶提取物中含有较多的黄酮物质,通过与第一整理 剂中的增强剂组合,具有高效的抗菌性能和抗紫外线性能,从而增强抗菌面料的抗菌性和断 裂强力;对比实验样品1和实验样品10-11可知,杏仁粉加入后,抗菌面料的抗皱性能有了 一定的提高,说明杏仁粉的加入可以增强抗菌面料的抗皱性;对比实验样品1和实验样品12-13可知,通过控制木棉纤维、莫代尔纤维、涤纶纤维的配比,有助于增强抗菌面料的抗皱 性能和断裂强力,莫代尔纤维、涤纶纤维以及木棉纤维三种纤维控制重量比后,既可以获得 柔软度较好的面料,也能增强抗菌面料的抗皱性能;对比实验样品1和实验样品14-15可知, 当第一整理剂中渗透剂采用脂肪醇聚氧乙烯醚、磺化琥珀酸二辛酯钠盐,增强剂采用聚乙烯 和膨润土,并加入苦丁茶提取物,第二整理剂中加入杏仁粉后,所制备得到的抗菌面料具有 更好的抗菌性能、抗皱性能以及柔韧性。
本具体实施例仅仅是对本申请的解释,其并不是对本申请的限制,本领域技术人员在 阅读完本说明书后可以根据需要对本实施例做出没有创造性贡献的修改,但只要在本申请的 权利要求范围内都受到专利法的保护。

Claims (10)

1.一种抗菌面料的制备方法,其特征在于,包括以下步骤:
S1:将纤维经过第一整理剂浸渍,浸渍后进行烘干,并将纤维进行编织,得到编织后的坯布;
S2:将编织后的坯布经过第二整理剂浸渍,浸渍后进行烘干;
S3:将步骤S2中烘干后的坯布浸渍于抗菌剂中浸渍,浸渍后进行烘干;
S4:将步骤S3中烘干后的坯布进行清洗、烘干后得到该抗菌面料;
所述纤维由木棉纤维、莫代尔纤维和涤纶纤维组成;
所述第一整理剂包括以下重量份的原料:
乙二醛1-2份;
乙二醇0.5-1份;
氯化钙2-3份;
渗透剂2-5份;
增强剂1-1.5份;
水90-100份;
所述抗菌剂由以下重量份的组分组成:
季铵盐1-2份;
水溶性壳聚糖3-4份;
金银花提取物0.5-1份;
薄荷醇0.5-1份;
水90-110份。
2.根据权利要求1所述的一种抗菌面料的制备方法,其特征在于,所述渗透剂包括脂肪醇聚氧乙烯醚、磺化琥珀酸二辛酯钠盐中的至少一种。
3.根据权利要求1所述的一种抗菌面料的制备方法,其特征在于,所述增强剂由聚乙烯和膨润土组成。
4.根据权利要求1所述的一种抗菌面料的制备方法,其特征在于,所述第一整理剂的原料中还包括重量份数为0.5-1份的苦丁茶提取物。
5.根据权利要求1所述的一种抗菌面料的制备方法,其特征在于,所述第二整理剂包括以下重量份的原料:
柠檬酸1-2份;
碳羟基聚硅氧烷1-1.5份;
丝素蛋白0.5-0.8份;
水80-100份。
6.根据权利要求5所述的一种抗菌面料的制备方法,其特征在于,所述第二整理剂中还包括重量份数为0.1-0.2份的杏仁粉。
7.根据权利要求1所述的一种抗菌面料的制备方法,其特征在于,所述木棉纤维、莫代尔纤维以及涤纶纤维的重量比为1:2:(1-2)。
8.根据权利要求1所述的一种抗菌面料,其特征在于,所述步骤S1中的浸渍时间为3-5h、浸渍温度为70-90℃。
9.根据权利要求1所述的一种抗菌面料的制备方法,其特征在于,所述步骤S2中的浸渍时间2-3h,浸渍温度为50-60℃。
10.一种面料,其特征在于,通过如权利要求1-9中任意一项所述的抗菌面料的制备方法制得。
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