CN106351010A - 亚麻织物纱线的浆纱工艺 - Google Patents
亚麻织物纱线的浆纱工艺 Download PDFInfo
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Abstract
本发明公开了一种亚麻织物纱线的浆纱工艺,包括如下步骤:1)将1~2重量份聚氧乙烯油酸酯、0.8重量份过硫酸钾、2.3重量份水溶性聚丙烯酸、1.2重量份羟丙基甲基纤维素、11重量份变性淀粉依次投入35重量份去离子水中,搅拌均匀;2)再依次投入1.5重量份聚乙二醇双硬脂酸酯、0.8重量份胰加漂T、1.1重量份磷酸、0.6重量份三唑酮,继续搅拌,至充分混合均匀,制得浆液;3)将纱线浸入浆液上浆,压去余液,烘干。本发明上浆后纱线毛羽贴伏、强力显着提高,耐磨好,纱线的保伸性能好。
Description
技术领域
本发明涉及亚麻织物纱线的浆纱工艺。
背景技术
棉、粘胶以及合成纤维等织物的经纱,在织造前大都先经过浆纱;而现有浆纱用浆液的性能有待改进。
发明内容
本发明的目的在于提供一种亚麻织物纱线的浆纱工艺,其上浆后纱线毛羽贴伏、强力显着提高,耐磨好,纱线的保伸性能好。
为实现上述目的,本发明的技术方案是设计一种亚麻织物纱线的浆纱工艺,包括如下步骤:
1)将1~2重量份聚氧乙烯油酸酯、0.8重量份过硫酸钾、2.3重量份水溶性聚丙烯酸、1.2重量份羟丙基甲基纤维素、11重量份变性淀粉依次投入35重量份去离子水中,搅拌均匀;
2)再依次投入1.5重量份聚乙二醇双硬脂酸酯、0.8重量份胰加漂T、1.1重量份磷酸、0.6重量份三唑酮,继续搅拌,至充分混合均匀,制得浆液;
3)将纱线浸入浆液上浆,压去余液,烘干。
优选的,亚麻织物纱线的浆纱工艺,包括如下步骤:
1)将1重量份聚氧乙烯油酸酯、0.8重量份过硫酸钾、2.3重量份水溶性聚丙烯酸、1.2重量份羟丙基甲基纤维素、11重量份变性淀粉依次投入35重量份去离子水中,搅拌均匀;
2)再依次投入1.5重量份聚乙二醇双硬脂酸酯、0.8重量份胰加漂T、1.1重量份磷酸、0.6重量份三唑酮,继续搅拌,至充分混合均匀,制得浆液;
3)将纱线浸入浆液上浆,压去余液,烘干。
优选的,亚麻织物纱线的浆纱工艺,包括如下步骤:
1)将2重量份聚氧乙烯油酸酯、0.8重量份过硫酸钾、2.3重量份水溶性聚丙烯酸、1.2重量份羟丙基甲基纤维素、11重量份变性淀粉依次投入35重量份去离子水中,搅拌均匀;
2)再依次投入1.5重量份聚乙二醇双硬脂酸酯、0.8重量份胰加漂T、1.1重量份磷酸、0.6重量份三唑酮,继续搅拌,至充分混合均匀,制得浆液;
3)将纱线浸入浆液上浆,压去余液,烘干。
优选的,亚麻织物纱线的浆纱工艺,包括如下步骤:
1)将1.2重量份聚氧乙烯油酸酯、0.8重量份过硫酸钾、2.3重量份水溶性聚丙烯酸、1.2重量份羟丙基甲基纤维素、11重量份变性淀粉依次投入35重量份去离子水中,搅拌均匀;
2)再依次投入1.5重量份聚乙二醇双硬脂酸酯、0.8重量份胰加漂T、1.1重量份磷酸、0.6重量份三唑酮,继续搅拌,至充分混合均匀,制得浆液;
3)将纱线浸入浆液上浆,压去余液,烘干。
本发明的优点和有益效果在于:提供一种亚麻织物纱线的浆纱工艺,其上浆后纱线毛羽贴伏、强力显着提高,耐磨好,纱线的保伸性能好。
“退浆液”的性能和用途是由其组分及配比所决定的,且“退浆液”中的不同组分会相互影响,组分及其配比会决定“退浆液”的最终性能,如果组分及其配比不相互协调,单个组分所带来的有益效果,会被其他组分消减甚至消除,严重的时候,不同组分相互抵触,起不到整体综合作用,产生负作用和次品。本发明通过大量创造性劳动、反复验证,得到“退浆液”的最优组分及配比,使得多个组分综合在一起、相互协调、并产生正向综合效应。
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。
本发明具体实施的技术方案是:
实施例1
亚麻织物纱线的浆纱工艺,包括如下步骤:
1)将1~2重量份聚氧乙烯油酸酯、0.8重量份过硫酸钾、2.3重量份水溶性聚丙烯酸、1.2重量份羟丙基甲基纤维素、11重量份变性淀粉依次投入35重量份去离子水中,搅拌均匀;
2)再依次投入1.5重量份聚乙二醇双硬脂酸酯、0.8重量份胰加漂T、1.1重量份磷酸、0.6重量份三唑酮,继续搅拌,至充分混合均匀,制得浆液;
3)将纱线浸入浆液上浆,压去余液,烘干。
实施例2
亚麻织物纱线的浆纱工艺,包括如下步骤:
1)将1重量份聚氧乙烯油酸酯、0.8重量份过硫酸钾、2.3重量份水溶性聚丙烯酸、1.2重量份羟丙基甲基纤维素、11重量份变性淀粉依次投入35重量份去离子水中,搅拌均匀;
2)再依次投入1.5重量份聚乙二醇双硬脂酸酯、0.8重量份胰加漂T、1.1重量份磷酸、0.6重量份三唑酮,继续搅拌,至充分混合均匀,制得浆液;
3)将纱线浸入浆液上浆,压去余液,烘干。
实施例3
亚麻织物纱线的浆纱工艺,包括如下步骤:
1)将2重量份聚氧乙烯油酸酯、0.8重量份过硫酸钾、2.3重量份水溶性聚丙烯酸、1.2重量份羟丙基甲基纤维素、11重量份变性淀粉依次投入35重量份去离子水中,搅拌均匀;
2)再依次投入1.5重量份聚乙二醇双硬脂酸酯、0.8重量份胰加漂T、1.1重量份磷酸、0.6重量份三唑酮,继续搅拌,至充分混合均匀,制得浆液;
3)将纱线浸入浆液上浆,压去余液,烘干。
实施例4
亚麻织物纱线的浆纱工艺,包括如下步骤:
1)将1.2重量份聚氧乙烯油酸酯、0.8重量份过硫酸钾、2.3重量份水溶性聚丙烯酸、1.2重量份羟丙基甲基纤维素、11重量份变性淀粉依次投入35重量份去离子水中,搅拌均匀;
2)再依次投入1.5重量份聚乙二醇双硬脂酸酯、0.8重量份胰加漂T、1.1重量份磷酸、0.6重量份三唑酮,继续搅拌,至充分混合均匀,制得浆液;
3)将纱线浸入浆液上浆,压去余液,烘干。
上述各实施例上浆后纱线毛羽贴伏、强力显着提高,耐磨好,纱线的保伸性能好。
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.亚麻织物纱线的浆纱工艺,其特征在于,包括如下步骤:
1)将1~2重量份聚氧乙烯油酸酯、0.8重量份过硫酸钾、2.3重量份水溶性聚丙烯酸、1.2重量份羟丙基甲基纤维素、11重量份变性淀粉依次投入35重量份去离子水中,搅拌均匀;
2)再依次投入1.5重量份聚乙二醇双硬脂酸酯、0.8重量份胰加漂T、1.1重量份磷酸、0.6重量份三唑酮,继续搅拌,至充分混合均匀,制得浆液;
3)将纱线浸入浆液上浆,压去余液,烘干。
2.根据权利要求1所述的亚麻织物纱线的浆纱工艺,其特征在于,包括如下步骤:
1)将1重量份聚氧乙烯油酸酯、0.8重量份过硫酸钾、2.3重量份水溶性聚丙烯酸、1.2重量份羟丙基甲基纤维素、11重量份变性淀粉依次投入35重量份去离子水中,搅拌均匀;
2)再依次投入1.5重量份聚乙二醇双硬脂酸酯、0.8重量份胰加漂T、1.1重量份磷酸、0.6重量份三唑酮,继续搅拌,至充分混合均匀,制得浆液;
3)将纱线浸入浆液上浆,压去余液,烘干。
3.根据权利要求1所述的亚麻织物纱线的浆纱工艺,其特征在于,包括如下步骤:
1)将2重量份聚氧乙烯油酸酯、0.8重量份过硫酸钾、2.3重量份水溶性聚丙烯酸、1.2重量份羟丙基甲基纤维素、11重量份变性淀粉依次投入35重量份去离子水中,搅拌均匀;
2)再依次投入1.5重量份聚乙二醇双硬脂酸酯、0.8重量份胰加漂T、1.1重量份磷酸、0.6重量份三唑酮,继续搅拌,至充分混合均匀,制得浆液;
3)将纱线浸入浆液上浆,压去余液,烘干。
4.根据权利要求1所述的亚麻织物纱线的浆纱工艺,其特征在于,包括如下步骤:
1)将1.2重量份聚氧乙烯油酸酯、0.8重量份过硫酸钾、2.3重量份水溶性聚丙烯酸、1.2重量份羟丙基甲基纤维素、11重量份变性淀粉依次投入35重量份去离子水中,搅拌均匀;
2)再依次投入1.5重量份聚乙二醇双硬脂酸酯、0.8重量份胰加漂T、1.1重量份磷酸、0.6重量份三唑酮,继续搅拌,至充分混合均匀,制得浆液;
3)将纱线浸入浆液上浆,压去余液,烘干。
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