CN115627630B - 一种抗起球面料及其制备方法和应用 - Google Patents
一种抗起球面料及其制备方法和应用 Download PDFInfo
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- 239000004744 fabric Substances 0.000 title claims abstract description 104
- 238000002360 preparation method Methods 0.000 title claims abstract description 36
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 239000000835 fiber Substances 0.000 claims abstract description 49
- 229920000728 polyester Polymers 0.000 claims abstract description 37
- 238000000034 method Methods 0.000 claims abstract description 29
- 239000007788 liquid Substances 0.000 claims abstract description 26
- 238000002156 mixing Methods 0.000 claims abstract description 20
- 210000002268 wool Anatomy 0.000 claims abstract description 20
- 239000002202 Polyethylene glycol Substances 0.000 claims abstract description 19
- 229920001223 polyethylene glycol Polymers 0.000 claims abstract description 19
- -1 hydroxybutyl Chemical group 0.000 claims abstract description 16
- 239000002994 raw material Substances 0.000 claims abstract description 15
- GFIHKCBJSYGAPP-UHFFFAOYSA-N [Cl-].C(=O)=CC[PH+](CC=C=O)CC=C=O Chemical compound [Cl-].C(=O)=CC[PH+](CC=C=O)CC=C=O GFIHKCBJSYGAPP-UHFFFAOYSA-N 0.000 claims abstract description 14
- 238000001035 drying Methods 0.000 claims abstract description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 13
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 12
- 229920001730 Moisture cure polyurethane Polymers 0.000 claims abstract description 12
- 229910021389 graphene Inorganic materials 0.000 claims abstract description 12
- 239000000243 solution Substances 0.000 claims abstract description 12
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 claims abstract description 11
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 claims abstract description 11
- 229920001661 Chitosan Polymers 0.000 claims abstract description 11
- 235000012538 ammonium bicarbonate Nutrition 0.000 claims abstract description 11
- 239000001099 ammonium carbonate Substances 0.000 claims abstract description 11
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 claims abstract description 10
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims abstract description 10
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- 229920000056 polyoxyethylene ether Polymers 0.000 claims abstract description 10
- 150000002191 fatty alcohols Chemical class 0.000 claims abstract description 9
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- 239000004205 dimethyl polysiloxane Substances 0.000 claims abstract description 8
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- 239000008367 deionised water Substances 0.000 claims abstract description 6
- 229910021641 deionized water Inorganic materials 0.000 claims abstract description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 29
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 24
- 238000006243 chemical reaction Methods 0.000 claims description 18
- 239000011734 sodium Substances 0.000 claims description 15
- 229910052708 sodium Inorganic materials 0.000 claims description 15
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 claims description 14
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 14
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 12
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 12
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 11
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- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims description 10
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
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- JVLRYPRBKSMEBF-UHFFFAOYSA-K diacetyloxystibanyl acetate Chemical compound [Sb+3].CC([O-])=O.CC([O-])=O.CC([O-])=O JVLRYPRBKSMEBF-UHFFFAOYSA-K 0.000 claims description 7
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- 229920004933 Terylene® Polymers 0.000 claims description 5
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 claims description 5
- 239000012975 dibutyltin dilaurate Substances 0.000 claims description 5
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- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 claims description 5
- 238000004804 winding Methods 0.000 claims description 5
- LWKJNIMGNUTZOO-UHFFFAOYSA-M 3,5-dichloro-2-hydroxybenzenesulfonate Chemical compound OC1=C(Cl)C=C(Cl)C=C1S([O-])(=O)=O LWKJNIMGNUTZOO-UHFFFAOYSA-M 0.000 claims description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 3
- 229940077386 sodium benzenesulfonate Drugs 0.000 claims description 3
- 238000000643 oven drying Methods 0.000 claims description 2
- 230000035699 permeability Effects 0.000 abstract description 34
- 238000010521 absorption reaction Methods 0.000 abstract description 13
- 230000000052 comparative effect Effects 0.000 description 17
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- 229920002635 polyurethane Polymers 0.000 description 11
- 239000004814 polyurethane Substances 0.000 description 11
- NMWCVZCSJHJYFW-UHFFFAOYSA-M sodium;3,5-dichloro-2-hydroxybenzenesulfonate Chemical compound [Na+].OC1=C(Cl)C=C(Cl)C=C1S([O-])(=O)=O NMWCVZCSJHJYFW-UHFFFAOYSA-M 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- 239000004753 textile Substances 0.000 description 6
- 125000003396 thiol group Chemical group [H]S* 0.000 description 6
- 238000001514 detection method Methods 0.000 description 5
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- 230000009286 beneficial effect Effects 0.000 description 3
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- 238000004090 dissolution Methods 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- IULJSGIJJZZUMF-UHFFFAOYSA-N 2-hydroxybenzenesulfonic acid Chemical compound OC1=CC=CC=C1S(O)(=O)=O IULJSGIJJZZUMF-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 125000005439 maleimidyl group Chemical group C1(C=CC(N1*)=O)=O 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 238000006068 polycondensation reaction Methods 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- PBVAJRFEEOIAGW-UHFFFAOYSA-N 3-[bis(2-carboxyethyl)phosphanyl]propanoic acid;hydrochloride Chemical compound Cl.OC(=O)CCP(CCC(O)=O)CCC(O)=O PBVAJRFEEOIAGW-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
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- 239000011148 porous material Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
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- D—TEXTILES; PAPER
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- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/244—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus
- D06M13/282—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus with compounds containing phosphorus
- D06M13/285—Phosphines; Phosphine oxides; Phosphine sulfides; Phosphinic or phosphinous acids or derivatives thereof
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/68—Polyesters containing atoms other than carbon, hydrogen and oxygen
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- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
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- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/10—Other agents for modifying properties
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- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/88—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds
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Abstract
本申请涉及服装面料领域,具体公开了一种抗起球面料及其制备方法和应用,其制备方法包括以下步骤:将改性涤纶纤维和羊毛纤维混纺,得到面料;将面料首先进行预处理,将面料置于三(2‑羰基乙基)磷盐酸盐溶液中进行预处理;将预处理后的面料置于整理液中,整理液由包括以下原料制得:甲氧基聚乙二醇马来酰亚胺、聚氨酯预聚体、氧化石墨烯、二端羟丁基聚二甲基硅氧烷、壳聚糖、碳酸氢铵以及脂肪醇聚氧乙烯醚;清洗干燥:用去离子水清洗、自然干燥,然后烘焙,得到抗起球面料;本申请还公开了通过上述方法制得的抗起球面料及其在服装领域的应用,本申请具有改善涤纶羊毛混纺面料的抗起毛球性能,同时具有优异的吸湿透气性能的特点。
Description
技术领域
本申请涉及服装面料技术领域,更具体地说,它涉及一种抗起球面料及其制备方法和应用。
背景技术
随着现代纺织技术不断发展和人们对生活需求的提升,服装的舒适性与功能性越来越受到消费者的重视。普通涤纶(聚酯纤维)面料具有弹性好、挺括抗皱、保形性好,以及优良的洗可穿性和耐用性等性能,被广泛用于制作各类服装。羊毛纤维是一种天然的蛋白质纤维,具有特殊的卷曲性,因此羊毛织物具有保暖性好、弹性优、透气透湿等优点,在纺织领域被广泛应用。羊毛纤维和涤纶的混纺面料挺括有立体感,柔软度和弹性较好,质地厚实,防寒保暖性良好,是纺织领域常用的一种面料。
然而,羊毛纤维表面具有特殊的鳞片结构,在外力的作用下易发生定向摩擦效应,因此羊毛织物易因摩擦作用发生起毛起球现象,影响了织物的外观和服用性,而涤纶原料也更加容易起球,因而改善羊毛纤维和涤纶的混纺面料的抗起毛起球性能对于其产品的发展具有重大的实际意义。
现有市售树脂型整理剂会使得被整理织物的手感恶化,严重影响织物的透气和吸湿性能,从而影响织物的服用舒适性。研究赋予涤棉针织物优良抗起毛球性能,而又不明显吸湿透气性能的技术,具有重要的现实意义。
发明内容
为了改善涤纶羊毛混纺面料的抗起毛球性能,同时具有优异的吸湿透气性能,本申请提供一种抗起球面料及其制备方法和应用。
第一方面,本申请提供一种抗起球面料的制备方法,采用如下的技术方案:
一种抗起球面料的制备方法,包括以下步骤:
混纺:将改性涤纶纤维和羊毛纤维混纺,得到面料;
预处理:将面料首先进行预处理,将面料置于三(2-羰基乙基)磷盐酸盐溶液中进行预处理;
后整理:将预处理后的面料置于整理液中,整理液由包括以下重量份的原料制得:20-30份甲氧基聚乙二醇马来酰亚胺、50-70份聚氨酯预聚体、6-12份氧化石墨烯、15-20份二端羟丁基聚二甲基硅氧烷、10-20份壳聚糖、8-15份碳酸氢铵以及15-20份脂肪醇聚氧乙烯醚;
清洗干燥:用去离子水清洗、自然干燥,然后烘焙,得到抗起球面料。
通过采用上述技术方案,本申请中整理主要采用有机硅改性聚氨酯实现,聚氨酯与纤维交联成膜,在外力作用时不易起毛,而且其沉淀在纤维与纤维之间的孔隙中,减少纤维间的相对滑移,达到抗起毛球的效果。二端羟丁基聚二甲基硅氧烷有机硅和壳聚糖对聚氨酯进行改性,使得整理后织物具有更好的抗起毛起球性能的同时,对于织物手感影响较小。
但是由于羊毛纤维中鳞片层的结构,尤其是鳞片层具有疏水性以及二硫键的保护作用,导致改性聚氨酯在纤维上的附着牢度低,在外力摩擦和水洗过程中容易脱落,失去抗起毛球效果。
因此本申请中首先将面料置于三(2-羰基乙基)磷盐酸盐溶液中预处理的时候,对羊毛纤维中的二硫键还原为巯基,然后将其置于整理液中的时候,还原的巯基与甲氧基聚乙二醇马来酰亚胺中的马来酰亚胺基团特异性反应形成S-C键,提高面料的亲水性,从而使得有机硅改性聚氨酯整理剂在纤维上附着牢度增大,在外力摩擦和水洗过程中不容易脱落,起到优异的抗起毛球效果,而且提高面料的吸湿性能。
另外巯基也可以与氧化石墨烯表面的羧酸和羟基官能团作用,而氧化石墨烯和壳聚糖中利用其含氧官能团与聚氨酯形成嵌段聚合物,实现整理剂与纤维织物化学键合,连接更为牢固,不易脱落,起到更好的抗毛球效果,碳酸氢铵的添加使得面料在整理剂中浸泡后烘干,在整理剂层形成孔洞结构,从而改善由于整理剂涂层导致面料透气性差的现象,脂肪醇聚氧乙烯醚的添加更加有利于体系各个原料的均匀分散。最终制得的面料具有优异的抗起毛球性能的同时,对于透气吸湿性能影响更小,还具有良好的透气吸湿性能。
可选的,所述改性涤纶由以下重量份原料制得:
30-50份对苯二甲酸二甲酯、25-35份乙二醇、10-15份3,5-二氯-2-羟基苯磺酸钠、8-15份聚乙二醇、1-3份三乙胺、1-3份醋酸锑和18-25份聚乙烯醇。
可选的,所述改性涤纶纤维通过以下方法制得:
将对苯二甲酸二甲酯、乙二醇和3,5-二氯-2-羟基苯磺酸钠与聚乙二醇以及三乙胺在180-190℃下反应1-2h,然后加入醋酸锑,加热至220-240℃,抽真空条件下反应1-1.5h后加入聚乙烯醇,然后继续反应0.5-1h,得到PET熔体,然后经过挤出、冷却、上油、拉伸、热定型和卷绕制得改性涤纶。
通过采用上述技术方案,将3,5-二氯-2-羟基苯磺酸钠作为第三单体,聚乙二醇作为第四单体参与PET聚合生产过程,三乙胺作为酯交换催化剂,3,5-二氯-2-羟基苯磺酸钠的引入改善聚酯纤维的吸湿性能,然后缩聚之后加入聚乙烯醇,实现聚酯与聚乙烯醇聚合物的混合,得到的改性涤纶纤维具有更加优异的抗起球特性。
可选的,所述聚氨酯预聚体通过以下方法制得:
以重量份数计,将40-50份聚四氢呋喃醚二醇与8-15份二月桂酸二丁基锡和20-25份丁酮混合,升温至70℃,在氮气保护气氛下加入100-120份2,4-甲苯二异氰酸酯,保温反应1-2h后,降温至50℃,然后加入15-25份N-羟甲基二乙醇胺和30-40份1,4-丁二醇和3-8份间苯二甲酸二甲酯-5-磺酸钠,保温反应1-2h。
通过采用上述技术方案,聚氨酯预聚体中间苯二甲酸二甲酯-5-磺酸钠的引入磺酸基基团,改善后整理后织物的亲水性能,从而具有更加优异的吸湿性能。
可选的,混纺步骤中,所述改性涤纶纤维和羊毛纤维以质量比为(6-7):1混纺。
可选的,预处理步骤中,按照浴比1:(20-30)、在40-50℃下保温振荡浸泡20-30min,然后烘干。
可选的,后整理步骤中,面料与整理液的浴比为1:(30-40)、在40-50℃下保温振荡浸泡20-30min,然后进行清洗干燥。
第二方面,本申请提供一种抗起球面料,采用如下的技术方案:
一种抗起球面料,通过所述制备方法制得的抗起球面料。
通过采用上述技术方案,通过本申请方法制得的面料具有优异抗起球性能的同时,还具有优异的吸湿透气性,具有优良的穿着舒适性。
第三方面,本申请提供一种抗起球面料在服装中的应用。
综上所述,本申请具有以下有益效果:
1、本申请中首先将面料置于三(2-羰基乙基)磷盐酸盐溶液中预处理的时候,对羊毛纤维中的二硫键还原为巯基,然后将其置于整理液中的时候,还原的巯基与甲氧基聚乙二醇马来酰亚胺中的马来酰亚胺基团特异性反应形成S-C键,提高面料的亲水性,从而使得有机硅改性聚氨酯整理剂在纤维上附着牢度增大,在外力摩擦和水洗过程中不容易脱落,起到优异的抗起毛球效果,而且提高面料的吸湿性能;
2、本申请中还原后的巯基与氧化石墨烯表面的羧酸和羟基官能团作用,而氧化石墨烯和壳聚糖中利用其含氧官能团与聚氨酯形成嵌段聚合物,实现整理剂与纤维织物化学键合,连接更为牢固,不易脱落,起到更好的抗毛球效果;
3、本申请中碳酸氢铵的添加使得面料在整理剂中浸泡后烘干,在整理剂层形成孔洞结构,从而改善由于整理剂涂层导致面料透气性差的现象,脂肪醇聚氧乙烯醚的添加更加有利于体系各个原料的均匀分散。最终制得的面料具有优异的抗起毛球性能的同时,对于透气吸湿性能影响更小,还具有良好的透气吸湿性能;
4、本申请中将3,5-二氯-2-羟基苯磺酸钠作为第三单体,聚乙二醇作为第四单体参与PET聚合生产过程,缩聚之后加入聚乙烯醇,实现聚酯与聚乙烯醇聚合物的混合,得到的改性涤纶纤维具有更加优异的抗起球特性。
具体实施方式
以下结合实施例对本申请作进一步详细说明,予以特别说明的是:以下实施例中未注明具体条件者,按照常规条件或制造商建议的条件进行,以下实施例中所用原料除特殊说明外均可来源于普通市售。
以下制备例为改性涤纶的制备例
制备例1
一种改性涤纶纤维通过以下方法制得:
将40kg对苯二甲酸二甲酯、30kg乙二醇和12kg3,5-二氯-2-羟基苯磺酸钠与10kg聚乙二醇以及2kg三乙胺在185℃下反应1.5h,然后加入2kg醋酸锑,加热至230℃,抽真空条件下反应1h后加入20kg聚乙烯醇,然后继续反应40min,得到PET熔体,然后经过挤出、冷却、上油、拉伸、热定型和卷绕制得改性涤纶。
制备例2
一种改性涤纶纤维通过以下方法制得:
将30kg对苯二甲酸二甲酯、25kg乙二醇和10kg3,5-二氯-2-羟基苯磺酸钠与8kg聚乙二醇以及1kg三乙胺在180℃下反应2h,然后加入1kg醋酸锑,加热至220℃,抽真空条件下反应1.5h后加入18kg聚乙烯醇,然后继续反应1h,得到PET熔体,然后经过挤出、冷却、上油、拉伸、热定型和卷绕制得改性涤纶。
制备例3
一种改性涤纶纤维通过以下方法制得:
将50kg对苯二甲酸二甲酯、35kg乙二醇和15kg3,5-二氯-2-羟基苯磺酸钠与15kg聚乙二醇以及3kg三乙胺在190℃下反应1h,然后加入3kg醋酸锑,加热至240℃,抽真空条件下反应1h后加入25kg聚乙烯醇,然后继续反应1h,得到PET熔体,然后经过挤出、冷却、上油、拉伸、热定型和卷绕制得改性涤纶。
制备例4
一种改性涤纶纤维按照制备例1中的方法进行,不同之处在于,原料中未添加3,5-二氯-2-羟基苯磺酸钠和聚乙烯醇。
制备例5
一种改性涤纶纤维按照制备例1中的方法进行,不同之处在于,3,5-二氯-2-羟基苯磺酸钠等量替换为间苯二甲酸二甲酯-5-磺酸钠。
制备例6
一种改性涤纶纤维按照制备例1中的方法进行,不同之处在于,原料中未添加聚乙烯醇。
制备例7
一种改性涤纶纤维按照制备例1中的方法进行,不同之处在于,原料中未添加3,5-二氯-2-羟基苯磺酸钠。
实施例
实施例1
一种抗起球面料的制备方法,包括以下步骤:
S1、混纺:将制备例1中得到的改性涤纶纤维和羊毛纤维以质量比为6:1混纺,得到面料;
S2、预处理:将面料首先按照浴比1:25置于三(2-羰基乙基)磷盐酸盐溶液中,在45℃下保温振荡浸泡25min,然后烘干,三(2-羰基乙基)磷盐酸盐溶液由三(2-羰基乙基)磷盐酸盐与水按照质量比为1:13混合而成;
S3、后整理:将预处理后的面料置于整理液中,整理液由包括以下原料混合后按照50g/L用量溶解于水中:25kg甲氧基聚乙二醇马来酰亚胺、60kg聚氨酯预聚体、10kg氧化石墨烯、18kg二端羟丁基聚二甲基硅氧烷、15kg壳聚糖、10kg碳酸氢铵以及18kg脂肪醇聚氧乙烯醚,面料与溶解后整理液按照浴比为1:35浸泡,在45℃下保温振荡浸泡25min,浸轧;
其中,聚氨酯预聚体通过以下方法制得:
将45kg聚四氢呋喃醚二醇与10kg二月桂酸二丁基锡和22kg丁酮混合,升温至70℃,在氮气保护气氛下加入110kg2,4-甲苯二异氰酸酯,保温反应1.5h后,降温至50℃,然后加入20kgN-羟甲基二乙醇胺和35kg1,4-丁二醇和5kg间苯二甲酸二甲酯-5-磺酸钠,保温反应1-2h;
S4、清洗干燥:用去离子水清洗、自然干燥,然后在65℃烘焙,得到抗起球面料。
实施例2
一种抗起球面料的制备方法,包括以下步骤:
S1、混纺:将制备例2中得到的改性涤纶纤维和羊毛纤维以质量比为6:1混纺,得到面料;
S2、预处理:将面料首先按照浴比1:20置于三(2-羰基乙基)磷盐酸盐溶液中,在40℃下保温振荡浸泡30min,然后烘干,三(2-羰基乙基)磷盐酸盐溶液由三(2-羰基乙基)磷盐酸盐与水按照质量比为1:12混合而成;
S3、后整理:将预处理后的面料置于整理液中,整理液由包括以下原料混合后按照30g/L用量溶解于水中:20kg甲氧基聚乙二醇马来酰亚胺、50kg聚氨酯预聚体、6kg氧化石墨烯、15kg二端羟丁基聚二甲基硅氧烷、10kg壳聚糖、8kg碳酸氢铵以及15kg脂肪醇聚氧乙烯醚,面料与溶解后整理液按照浴比为1:30浸泡,在40℃下保温振荡浸泡30min,浸轧;
其中,聚氨酯预聚体通过以下方法制得:
将40kg聚四氢呋喃醚二醇与8kg二月桂酸二丁基锡和20kg丁酮混合,升温至70℃,在氮气保护气氛下加入100kg2,4-甲苯二异氰酸酯,保温反应1h后,降温至50℃,然后加入15kgN-羟甲基二乙醇胺和30kg1,4-丁二醇和3kg间苯二甲酸二甲酯-5-磺酸钠,保温反应1h;
S4、清洗干燥:用去离子水清洗、自然干燥,然后在60℃烘焙,得到抗起球面料。
实施例3
一种抗起球面料的制备方法,包括以下步骤:
S1、混纺:将制备例3中得到的改性涤纶纤维和羊毛纤维以质量比为7:1混纺,得到面料;
S2、预处理:将面料首先按照浴比1:30置于三(2-羰基乙基)磷盐酸盐溶液中,在50℃下保温振荡浸泡20min,然后烘干,三(2-羰基乙基)磷盐酸盐溶液由三(2-羰基乙基)磷盐酸盐与水按照质量比为1:15混合而成;
S3、后整理:将预处理后的面料置于整理液中,整理液由包括以下原料混合后按照70g/L用量溶解于水中:30kg甲氧基聚乙二醇马来酰亚胺、70kg聚氨酯预聚体、12kg氧化石墨烯、20kg二端羟丁基聚二甲基硅氧烷、20kg壳聚糖、15kg碳酸氢铵以及20kg脂肪醇聚氧乙烯醚,面料与溶解后整理液按照浴比为1:40浸泡,在50℃下保温振荡浸泡20min,浸轧;
其中,聚氨酯预聚体通过以下方法制得:
将50kg聚四氢呋喃醚二醇与15kg二月桂酸二丁基锡和25kg丁酮混合,升温至70℃,在氮气保护气氛下加入120kg2,4-甲苯二异氰酸酯,保温反应2h后,降温至50℃,然后加入25kgN-羟甲基二乙醇胺和40kg1,4-丁二醇和8kg间苯二甲酸二甲酯-5-磺酸钠,保温反应2h;
S4、清洗干燥:用去离子水清洗、自然干燥,然后在70℃烘焙,得到抗起球面料。
实施例4-7
一种抗起球面料的制备方法,按照实施例1中的方法进行,不同之处在于,步骤S1中的改性涤纶分别选用制备例4-7中制备得到的改性涤纶纤维。
对比例
对比例1
一种抗起球面料的制备方法,按照实施例1中的方法进行,不同之处在于,步骤S1中的改性涤纶纤维等量替换为涤纶纤维。
对比例2
一种抗起球面料的制备方法,按照实施例1中的方法进行,不同之处在于,未进行步骤S2的处理,步骤S1混纺后直接进行步骤S3的后整理步骤,且步骤S3整理液中未添加甲氧基聚乙二醇马来酰亚胺。
对比例3
一种抗起球面料的制备方法,按照实施例1中的方法进行,不同之处在于,步骤S3整理液中未添加二端羟丁基聚二甲基硅氧烷。
对比例4
一种抗起球面料的制备方法,按照实施例1中的方法进行,不同之处在于,步骤S3整理液中未添加氧化石墨烯。
对比例5
一种抗起球面料的制备方法,按照实施例1中的方法进行,不同之处在于,步骤S3整理液中未添加壳聚糖。
对比例6
一种抗起球面料的制备方法,按照实施例1中的方法进行,不同之处在于,步骤S3整理液中未添加碳酸氢铵。
对比例7
一种抗起球面料的制备方法,按照实施例1中的方法进行,不同之处在于,步骤S3整理液中未添加脂肪醇聚氧乙烯醚。
性能检测
对上述实施例和对比例中制得的面料进行抗起毛起球等级、吸湿性以及透气性能进行检测,其中抗起毛起球性能按照GB/T4802.1-1997纺织品织物起球试验圆轨迹法测试,透气性参照GB/T5453《纺织品织物透气性的测试》进行检测,透湿性参照GB/T12704.1-2009《纺织品织物透湿性试验方法》第一部分:吸湿法进行检测,检测结果如下表1和表2,其中表1是实施例检测结果,表2是对比例检测结果。
表1:
由上表1可知,本申请实施例1-3中制得的面料具有更加优异的抗起毛起球性能、透气性以及透湿性;结合实施例1与实施例4的检测结果,实施例4中未添加3,5-二氯-2-羟基苯磺酸钠和聚乙烯醇的时候,其抗起毛球性能降低的同时,透湿性能和透气性能也有所降低,尤其是透湿性能下降幅度较大,实施例5中将3,5-二氯-2-羟基苯磺酸钠等量替换为间苯二甲酸二甲酯-5-磺酸钠,再结合实施例7中未添加3,5-二氯-2-羟基苯磺酸钠的检测结果,可以看到实施例5和实施例7中的抗起毛球性能影响较小,但是对于透湿性能影响较大,实施例5中虽然都引入了磺酸基团,但是选用3,5-二氯-2-羟基苯磺酸钠相较于间苯二甲酸二甲酯-5-磺酸钠,其透湿性能更加优异,而且透气性能也更好,而未引入磺酸基团的时候,透湿性大大降低,不过相较于实施例4好,说明聚乙烯醇的引入不仅可以提高其抗起毛球性能,而且还可以提高其透湿性能。
参照上表2中的检测结果,结合实施例1与对比例1的检测结果,对比例1中选用普通涤纶的时候,抗起毛球性能差,而且透气性和透湿性也差;再结合对比例2的检测结果,未进行三(2-羰基乙基)磷盐酸盐溶液的预处理以及甲氧基聚乙二醇马来酰亚胺的处理,抗起毛球性能更差,而透湿性和透气性也稍有所降低;结合对比例3的检测结果,整理液中未通过有机硅改性的时候,抗起毛性能差,而且透湿性影响较大,透气性影响较小,而对比例4和对比例5中未添加氧化石墨烯或壳聚糖的时候,抗起毛球性能降低,且透湿性和透气性也有所降低;对比例6中未添加碳酸氢铵的时候,透气性显著降低,对比例7中未添加脂肪醇聚氧乙烯醚的时候,可能由于碳酸氢铵等在体系中的分散不均匀,导致产品的透气性和透湿性均有所降低。
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 (7)
1.一种抗起球面料的制备方法,其特征在于,包括以下步骤:
混纺:将改性涤纶纤维和羊毛纤维混纺,得到面料;
预处理:将面料首先进行预处理,将面料置于三(2-羰基乙基)磷盐酸盐溶液中进行预处理,按照浴比1:(20-30)、在40-50℃下保温振荡浸泡20-30min,然后烘干;
后整理:将预处理后的面料置于整理液中,整理液由包括以下重量份的原料制得:20-30份甲氧基聚乙二醇马来酰亚胺、50-70份聚氨酯预聚体、6-12份氧化石墨烯、15-20份二端羟丁基聚二甲基硅氧烷、10-20份壳聚糖、8-15份碳酸氢铵以及15-20份脂肪醇聚氧乙烯醚,面料与整理液的浴比为1:(30-40)、在40-50℃下保温振荡浸泡20-30min;
清洗干燥:用去离子水清洗、自然干燥,然后烘焙,得到抗起球面料。
2.根据权利要求1所述的一种抗起球面料的制备方法,其特征在于:所述改性涤纶由以下重量份原料制得:
30-50份对苯二甲酸二甲酯、25-35份乙二醇、10-15份3,5-二氯-2-羟基苯磺酸钠、8-15份聚乙二醇、1-3份三乙胺、1-3份醋酸锑和18-25份聚乙烯醇。
3.根据权利要求2所述的一种抗起球面料的制备方法,其特征在于:所述改性涤纶纤维通过以下方法制得:
将对苯二甲酸二甲酯、乙二醇和3,5-二氯-2-羟基苯磺酸钠与聚乙二醇以及三乙胺在180-190℃下反应1-2h,然后加入醋酸锑,加热至220-240℃,抽真空条件下反应1-1.5h后加入聚乙烯醇,然后继续反应0.5-1h,得到PET熔体,然后经过挤出、冷却、上油、拉伸、热定型和卷绕制得改性涤纶。
4.根据权利要求1所述的一种抗起球面料的制备方法,其特征在于:所述聚氨酯预聚体通过以下方法制得:
以重量份数计,将40-50份聚四氢呋喃醚二醇与8-15份二月桂酸二丁基锡和20-25份丁酮混合,升温至70℃,在氮气保护气氛下加入100-120份2,4-甲苯二异氰酸酯,保温反应1-2h后,降温至50℃,然后加入15-25份N-羟甲基二乙醇胺和30-40份1,4-丁二醇和3-8份间苯二甲酸二甲酯-5-磺酸钠,保温反应1-2h。
5.根据权利要求1所述的一种抗起球面料的制备方法,其特征在于:混纺步骤中,所述改性涤纶纤维和羊毛纤维以质量比为(6-7):1混纺。
6.一种通过权利要求1-5任意一项所述制备方法制得的抗起球面料。
7.如权利要求6所述的抗起球面料在服装中的应用。
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