CN107447511A - 一种抗皱耐顶破无纺布及其制备方法 - Google Patents
一种抗皱耐顶破无纺布及其制备方法 Download PDFInfo
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- 239000008367 deionised water Substances 0.000 claims abstract description 27
- 229910021641 deionized water Inorganic materials 0.000 claims abstract description 27
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 claims abstract description 24
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- 239000011592 zinc chloride Substances 0.000 claims abstract description 9
- 235000005074 zinc chloride Nutrition 0.000 claims abstract description 9
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- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 7
- 229910021578 Iron(III) chloride Inorganic materials 0.000 claims description 7
- 239000007864 aqueous solution Substances 0.000 claims description 7
- 238000006392 deoxygenation reaction Methods 0.000 claims description 7
- 238000003837 high-temperature calcination Methods 0.000 claims description 7
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 claims description 7
- 229910052757 nitrogen Inorganic materials 0.000 claims description 7
- 239000000843 powder Substances 0.000 claims description 7
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- WALYXZANOBBHCI-UHFFFAOYSA-K magnesium sodium trichloride hydrate Chemical compound O.[Cl-].[Na+].[Mg+2].[Cl-].[Cl-] WALYXZANOBBHCI-UHFFFAOYSA-K 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims 1
- 230000035699 permeability Effects 0.000 abstract description 4
- 229920002554 vinyl polymer Polymers 0.000 abstract description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 1
- 150000003953 γ-lactams Chemical class 0.000 abstract 1
- 239000004753 textile Substances 0.000 description 7
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- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 2
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Abstract
本发明公开了一种抗皱耐顶破无纺布及其制备方法,按重量份计,所述无纺布包括聚丙烯无纺布23~55份、壳聚糖13~22份、氯化铁11~25份、氯化锌9~18份、氯化镁6~22份、咖啡渣11~30份、聚酯23~40份、苯乙烯磺酸钠12~18份、N‑乙烯基‑2‑吡咯烷酮2~7份、丙烯酰胺3~8份、丙烯酸1~8份、去离子水22~45份。本发明所述抗皱耐顶破无纺布具有良好的保形性和包覆性;本发明所述抗皱耐顶破无纺布强力较大,能承受一定牵拉力,具有抗顶破和抗撕裂能力;本发明所述抗皱耐顶破无纺布吸湿透气性能好。
Description
技术领域
本发明属于材料化学领域,涉及一种功能性无纺布材料,具体为一种抗皱耐顶破无纺布及其制备方法。
背景技术
家用纺织品与服用纺织品、产业用纺织是构成纺织产品的三大基本要素。近年来,我国的纺织品服装生产规模居世界首位。随着时代的发展和人们生活水平的提高,我国的家用纺织品市场得到了长足的发展,家用纺织品业将成为未来消费增长点,而且今天的家用纺织品己从实用功能逐步向装饰、美化、保健等多功能方向发展。
从发展趋势上看,家用纺织品已成为一个整体消费门类,床垫布在这一门类中占有重要地位。床垫布包覆在床塾外层,由销钉固定,其各方面性能直接影响床垫的质量与档次。床垫布是覆盖床垫上层,所以床上面料较为特殊,除花型美观大方外,它的要求是:第一,具有良好的保形性和包覆性,凸感强;第二,强力较大,能承受一定牵拉力,具有抗顶破和抗撕裂能力;第三,吸湿透气性能好等。
发明内容
本发明解决的技术问题:为了克服现有技术的缺陷,获得一种具有良好的保形性和抗顶破、抗撕裂能力的无纺布,本发明提供了一种抗皱耐顶破无纺布及其制备方法。
技术方案:一种抗皱耐顶破无纺布,按重量份计,所述无纺布包括聚丙烯无纺布23~55份、壳聚糖13~22份、氯化铁11~25份、氯化锌9~18份、氯化镁6~22份、咖啡渣11~30份、聚酯23~40份、苯乙烯磺酸钠12~18份、N-乙烯基-2-吡咯烷酮2~7份、丙烯酰胺3~8份、丙烯酸1~8份、去离子水22~45份。
优选的,按重量份计,所述无纺布包括聚丙烯无纺布48份、壳聚糖19份、氯化铁21份、氯化锌14份、氯化镁18份、咖啡渣25份、聚酯36份、苯乙烯磺酸钠16份、N-乙烯基-2-吡咯烷酮5份、丙烯酰胺7份、丙烯酸6份、去离子水40份。
一种抗皱耐顶破无纺布的制备方法,所述方法包含以下步骤:
(1)将聚丙烯无纺布裁剪为10cm×10cm的样品,用无水乙醇洗净后25~55℃条件下烘干,并围绕玻璃棒卷成圆柱状后捆扎;
(2)25~40℃条件下,将苯乙烯磺酸钠、N-乙烯基-2-吡咯烷酮、丙烯酰胺溶于去离子水中,向其中滴加丙烯酸,混合均匀后置于4℃密封保存;
(3)将步骤(1)捆扎后的聚丙烯无纺布浸没在步骤(2)获得的溶液中,并转移至辐照管中,待抽真空和充氮除氧后密封辐照试管,并置于紫外光室中,在25~35℃条件下进行辐照;
(4)将壳聚糖溶解于醋酸溶液中,并将步骤(3)处理后的聚丙烯无纺布浸没在其中反应12~19小时,取出用去离子水洗净,室温晾干;
(5)将咖啡渣在1000~1200℃条件下高温煅烧制成晶体,将晶体研磨成规格为100~300nm的粉末,加入到聚酯溶液中,将步骤(4)处理后的聚丙烯无纺布浸没在上述溶液中,反应3~8小时;
(6)将步骤(5)处理后的无纺布先后用氯化铁水溶液、氯化锌水溶液、氯化镁水溶液冲洗,每种溶液冲洗3~5次,最后用去离子水洗净,真空干燥后制得。
优选的,步骤(1)中将聚丙烯无纺布裁剪为10cm×10cm的样品,用无水乙醇洗净后45℃条件下烘干,并围绕玻璃棒卷成圆柱状后捆扎。
优选的,步骤(2)中35℃条件下,将苯乙烯磺酸钠、N-乙烯基-2-吡咯烷酮、丙烯酰胺溶于去离子水中,向其中滴加丙烯酸,混合均匀后置于4℃密封保存。
优选的,步骤(3)中将步骤(1)捆扎后的聚丙烯无纺布浸没在步骤(2)获得的溶液中,并转移至辐照管中,待抽真空和充氮除氧后密封辐照试管,并置于紫外光室中,在28℃条件下进行辐照。
优选的,步骤(4)中将壳聚糖溶解于醋酸溶液中,并将步骤(3)处理后的聚丙烯无纺布浸没在其中反应17小时,取出用去离子水洗净,室温晾干。
优选的,步骤(5)中将咖啡渣在1150℃条件下高温煅烧制成晶体,将晶体研磨成规格为200nm的粉末,加入到聚酯溶液中,将步骤(4)处理后的聚丙烯无纺布浸没在上述溶液中,反应6小时。
优选的,步骤(6)中将步骤(5)处理后的无纺布先后用氯化铁水溶液、氯化锌水溶液、氯化镁水溶液冲洗,每种溶液冲洗4次,最后用去离子水洗净,真空干燥后制得。
有益效果:(1)本发明所述抗皱耐顶破无纺布具有良好的保形性和包覆性;(2)本发明所述抗皱耐顶破无纺布强力较大,能承受一定牵拉力,具有抗顶破和抗撕裂能力;(3)本发明所述抗皱耐顶破无纺布吸湿透气性能好。
具体实施方式
实施例1
一种抗皱耐顶破无纺布,按重量份计,所述无纺布包括聚丙烯无纺布23份、壳聚糖13份、氯化铁11份、氯化锌9份、氯化镁6份、咖啡渣11份、聚酯23份、苯乙烯磺酸钠12份、N-乙烯基-2-吡咯烷酮2份、丙烯酰胺3份、丙烯酸1份、去离子水22份。
一种抗皱耐顶破无纺布的制备方法,所述方法包含以下步骤:
(1)将聚丙烯无纺布裁剪为10cm×10cm的样品,用无水乙醇洗净后25℃条件下烘干,并围绕玻璃棒卷成圆柱状后捆扎;
(2)25℃条件下,将苯乙烯磺酸钠、N-乙烯基-2-吡咯烷酮、丙烯酰胺溶于去离子水中,向其中滴加丙烯酸,混合均匀后置于4℃密封保存;
(3)将步骤(1)捆扎后的聚丙烯无纺布浸没在步骤(2)获得的溶液中,并转移至辐照管中,待抽真空和充氮除氧后密封辐照试管,并置于紫外光室中,在25℃条件下进行辐照;
(4)将壳聚糖溶解于醋酸溶液中,并将步骤(3)处理后的聚丙烯无纺布浸没在其中反应12小时,取出用去离子水洗净,室温晾干;
(5)将咖啡渣在1000℃条件下高温煅烧制成晶体,将晶体研磨成规格为100的粉末,加入到聚酯溶液中,将步骤(4)处理后的聚丙烯无纺布浸没在上述溶液中,反应3小时;
(6)将步骤(5)处理后的无纺布先后用氯化铁水溶液、氯化锌水溶液、氯化镁水溶液冲洗,每种溶液冲洗3次,最后用去离子水洗净,真空干燥后制得。
实施例2
一种抗皱耐顶破无纺布,按重量份计,所述无纺布包括聚丙烯无纺布48份、壳聚糖19份、氯化铁21份、氯化锌14份、氯化镁18份、咖啡渣25份、聚酯36份、苯乙烯磺酸钠16份、N-乙烯基-2-吡咯烷酮5份、丙烯酰胺7份、丙烯酸6份、去离子水40份。
一种抗皱耐顶破无纺布的制备方法,所述方法包含以下步骤:
(1)将聚丙烯无纺布裁剪为10cm×10cm的样品,用无水乙醇洗净后45℃条件下烘干,并围绕玻璃棒卷成圆柱状后捆扎;
(2)35℃条件下,将苯乙烯磺酸钠、N-乙烯基-2-吡咯烷酮、丙烯酰胺溶于去离子水中,向其中滴加丙烯酸,混合均匀后置于4℃密封保存;
(3)将步骤(1)捆扎后的聚丙烯无纺布浸没在步骤(2)获得的溶液中,并转移至辐照管中,待抽真空和充氮除氧后密封辐照试管,并置于紫外光室中,在28℃条件下进行辐照;
(4)将壳聚糖溶解于醋酸溶液中,并将步骤(3)处理后的聚丙烯无纺布浸没在其中反应17小时,取出用去离子水洗净,室温晾干;
(5)将咖啡渣在1150℃条件下高温煅烧制成晶体,将晶体研磨成规格为200nm的粉末,加入到聚酯溶液中,将步骤(4)处理后的聚丙烯无纺布浸没在上述溶液中,反应6小时;
(6)将步骤(5)处理后的无纺布先后用氯化铁水溶液、氯化锌水溶液、氯化镁水溶液冲洗,每种溶液冲洗4次,最后用去离子水洗净,真空干燥后制得。
实施例3
一种抗皱耐顶破无纺布,按重量份计,所述无纺布包括聚丙烯无纺布55份、壳聚糖22份、氯化铁25份、氯化锌18份、氯化镁22份、咖啡渣30份、聚酯40份、苯乙烯磺酸钠18份、N-乙烯基-2-吡咯烷酮7份、丙烯酰胺8份、丙烯酸8份、去离子水45份。
一种抗皱耐顶破无纺布的制备方法,所述方法包含以下步骤:
(1)将聚丙烯无纺布裁剪为10cm×10cm的样品,用无水乙醇洗净后55℃条件下烘干,并围绕玻璃棒卷成圆柱状后捆扎;
(2)40℃条件下,将苯乙烯磺酸钠、N-乙烯基-2-吡咯烷酮、丙烯酰胺溶于去离子水中,向其中滴加丙烯酸,混合均匀后置于4℃密封保存;
(3)将步骤(1)捆扎后的聚丙烯无纺布浸没在步骤(2)获得的溶液中,并转移至辐照管中,待抽真空和充氮除氧后密封辐照试管,并置于紫外光室中,在35℃条件下进行辐照;
(4)将壳聚糖溶解于醋酸溶液中,并将步骤(3)处理后的聚丙烯无纺布浸没在其中反应19小时,取出用去离子水洗净,室温晾干;
(5)将咖啡渣在1200℃条件下高温煅烧制成晶体,将晶体研磨成规格为300nm的粉末,加入到聚酯溶液中,将步骤(4)处理后的聚丙烯无纺布浸没在上述溶液中,反应8小时;
(6)将步骤(5)处理后的无纺布先后用氯化铁水溶液、氯化锌水溶液、氯化镁水溶液冲洗,每种溶液冲洗5次,最后用去离子水洗净,真空干燥后制得。
对实施例1~3制备获得的抗皱耐顶破无纺布进行检测,结果如下表所示:
实施例1 | 实施例2 | 实施例3 | |
透气性/mm·S-1 | 1516.3 | 1612.5 | 1593.6 |
静态悬垂系数/% | 41.2 | 55.3 | 51.6 |
回复角/° | 2.8 | 3.1 | 3.0 |
顶破强力/N | 406.2 | 423.8 | 412.9 |
Claims (9)
1.一种抗皱耐顶破无纺布,其特征在于,按重量份计,所述无纺布包括聚丙烯无纺布23~55份、壳聚糖13~22份、氯化铁11~25份、氯化锌9~18份、氯化镁6~22份、咖啡渣11~30份、聚酯23~40份、苯乙烯磺酸钠12~18份、N-乙烯基-2-吡咯烷酮2~7份、丙烯酰胺3~8份、丙烯酸1~8份、去离子水22~45份。
2.根据权利要求1所述的一种抗皱耐顶破无纺布,其特征在于,按重量份计,所述无纺布包括聚丙烯无纺布48份、壳聚糖19份、氯化铁21份、氯化锌14份、氯化镁18份、咖啡渣25份、聚酯36份、苯乙烯磺酸钠16份、N-乙烯基-2-吡咯烷酮5份、丙烯酰胺7份、丙烯酸6份、去离子水40份。
3.权利要求1所述的一种抗皱耐顶破无纺布的制备方法,其特征在于,所述方法包含以下步骤:
(1)将聚丙烯无纺布裁剪为10cm×10cm的样品,用无水乙醇洗净后25~55℃条件下烘干,并围绕玻璃棒卷成圆柱状后捆扎;
(2)25~40℃条件下,将苯乙烯磺酸钠、N-乙烯基-2-吡咯烷酮、丙烯酰胺溶于去离子水中,向其中滴加丙烯酸,混合均匀后置于4℃密封保存;
(3)将步骤(1)捆扎后的聚丙烯无纺布浸没在步骤(2)获得的溶液中,并转移至辐照管中,待抽真空和充氮除氧后密封辐照试管,并置于紫外光室中,在25~35℃条件下进行辐照;
(4)将壳聚糖溶解于醋酸溶液中,并将步骤(3)处理后的聚丙烯无纺布浸没在其中反应12~19小时,取出用去离子水洗净,室温晾干;
(5)将咖啡渣在1000~1200℃条件下高温煅烧制成晶体,将晶体研磨成规格为100~300nm的粉末,加入到聚酯溶液中,将步骤(4)处理后的聚丙烯无纺布浸没在上述溶液中,反应3~8小时;
(6)将步骤(5)处理后的无纺布先后用氯化铁水溶液、氯化锌水溶液、氯化镁水溶液冲洗,每种溶液冲洗3~5次,最后用去离子水洗净,真空干燥后制得。
4.根据权利要求3所述的一种抗皱耐顶破无纺布的制备方法,其特征在于,步骤(1)中将聚丙烯无纺布裁剪为10cm×10cm的样品,用无水乙醇洗净后45℃条件下烘干,并围绕玻璃棒卷成圆柱状后捆扎。
5.根据权利要求3所述的一种抗皱耐顶破无纺布的制备方法,其特征在于,步骤(2)中35℃条件下,将苯乙烯磺酸钠、N-乙烯基-2-吡咯烷酮、丙烯酰胺溶于去离子水中,向其中滴加丙烯酸,混合均匀后置于4℃密封保存。
6.根据权利要求3所述的一种抗皱耐顶破无纺布的制备方法,其特征在于,步骤(3)中将步骤(1)捆扎后的聚丙烯无纺布浸没在步骤(2)获得的溶液中,并转移至辐照管中,待抽真空和充氮除氧后密封辐照试管,并置于紫外光室中,在28℃条件下进行辐照。
7.根据权利要求3所述的一种抗皱耐顶破无纺布的制备方法,其特征在于,步骤(4)中将壳聚糖溶解于醋酸溶液中,并将步骤(3)处理后的聚丙烯无纺布浸没在其中反应17小时,取出用去离子水洗净,室温晾干。
8.根据权利要求3所述的一种抗皱耐顶破无纺布的制备方法,其特征在于,步骤(5)中将咖啡渣在1150℃条件下高温煅烧制成晶体,将晶体研磨成规格为200nm的粉末,加入到聚酯溶液中,将步骤(4)处理后的聚丙烯无纺布浸没在上述溶液中,反应6小时。
9.根据权利要求3所述的一种抗皱耐顶破无纺布的制备方法,其特征在于,步骤(6)中将步骤(5)处理后的无纺布先后用氯化铁水溶液、氯化锌水溶液、氯化镁水溶液冲洗,每种溶液冲洗4次,最后用去离子水洗净,真空干燥后制得。
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