CN103643526B - A kind of method adopting Ludox to prepare crease-resistant COTTON FABRIC - Google Patents
A kind of method adopting Ludox to prepare crease-resistant COTTON FABRIC Download PDFInfo
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- CN103643526B CN103643526B CN201310676802.XA CN201310676802A CN103643526B CN 103643526 B CN103643526 B CN 103643526B CN 201310676802 A CN201310676802 A CN 201310676802A CN 103643526 B CN103643526 B CN 103643526B
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- 239000004744 fabric Substances 0.000 title claims abstract description 65
- 229920000742 Cotton Polymers 0.000 title claims abstract description 47
- 238000000034 method Methods 0.000 title claims abstract description 22
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 title description 2
- 230000001153 anti-wrinkle effect Effects 0.000 claims abstract description 51
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 36
- 238000001035 drying Methods 0.000 claims abstract description 22
- 239000002253 acid Substances 0.000 claims abstract description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000007788 liquid Substances 0.000 claims abstract description 18
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000003054 catalyst Substances 0.000 claims abstract description 14
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims abstract description 13
- 239000008367 deionised water Substances 0.000 claims abstract description 9
- 229910021641 deionized water Inorganic materials 0.000 claims abstract description 9
- 238000003756 stirring Methods 0.000 claims abstract description 6
- 230000037303 wrinkles Effects 0.000 claims description 13
- 238000005406 washing Methods 0.000 claims description 9
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical group OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 6
- 239000003999 initiator Substances 0.000 claims description 6
- 239000003223 protective agent Substances 0.000 claims description 6
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 claims description 5
- KMZHZAAOEWVPSE-UHFFFAOYSA-N 2,3-dihydroxypropyl acetate Chemical compound CC(=O)OCC(O)CO KMZHZAAOEWVPSE-UHFFFAOYSA-N 0.000 claims description 4
- 238000009998 heat setting Methods 0.000 claims description 4
- 238000005096 rolling process Methods 0.000 claims description 4
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Chemical group [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 claims description 4
- GGAUUQHSCNMCAU-ZXZARUISSA-N (2s,3r)-butane-1,2,3,4-tetracarboxylic acid Chemical compound OC(=O)C[C@H](C(O)=O)[C@H](C(O)=O)CC(O)=O GGAUUQHSCNMCAU-ZXZARUISSA-N 0.000 claims description 2
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 claims description 2
- PHOQVHQSTUBQQK-SQOUGZDYSA-N D-glucono-1,5-lactone Chemical compound OC[C@H]1OC(=O)[C@H](O)[C@@H](O)[C@@H]1O PHOQVHQSTUBQQK-SQOUGZDYSA-N 0.000 claims description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 2
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 claims description 2
- 229910052921 ammonium sulfate Inorganic materials 0.000 claims description 2
- 235000011130 ammonium sulphate Nutrition 0.000 claims description 2
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 claims description 2
- 235000012209 glucono delta-lactone Nutrition 0.000 claims description 2
- 229960003681 gluconolactone Drugs 0.000 claims description 2
- 239000011976 maleic acid Substances 0.000 claims description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid group Chemical group C(\C=C/C(=O)O)(=O)O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 2
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- 229910000403 monosodium phosphate Inorganic materials 0.000 claims description 2
- 235000019799 monosodium phosphate Nutrition 0.000 claims description 2
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 claims description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 2
- JTXMVXSTHSMVQF-UHFFFAOYSA-N 2-acetyloxyethyl acetate Chemical compound CC(=O)OCCOC(C)=O JTXMVXSTHSMVQF-UHFFFAOYSA-N 0.000 claims 1
- ORVGYTXFUWTWDM-UHFFFAOYSA-N silicic acid;sodium Chemical group [Na].O[Si](O)(O)O ORVGYTXFUWTWDM-UHFFFAOYSA-N 0.000 claims 1
- 238000002791 soaking Methods 0.000 claims 1
- 239000001488 sodium phosphate Substances 0.000 claims 1
- 229910000162 sodium phosphate Inorganic materials 0.000 claims 1
- 235000011008 sodium phosphates Nutrition 0.000 claims 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 claims 1
- 230000014759 maintenance of location Effects 0.000 abstract description 9
- 230000007423 decrease Effects 0.000 abstract description 4
- 239000000243 solution Substances 0.000 description 24
- KWSLGOVYXMQPPX-UHFFFAOYSA-N 5-[3-(trifluoromethyl)phenyl]-2h-tetrazole Chemical compound FC(F)(F)C1=CC=CC(C2=NNN=N2)=C1 KWSLGOVYXMQPPX-UHFFFAOYSA-N 0.000 description 7
- 239000000835 fiber Substances 0.000 description 7
- 229910001379 sodium hypophosphite Inorganic materials 0.000 description 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 238000007598 dipping method Methods 0.000 description 4
- 150000003384 small molecules Chemical class 0.000 description 4
- 229920001410 Microfiber Polymers 0.000 description 3
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- 239000011148 porous material Substances 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical compound [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 239000004753 textile Substances 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
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- 210000001724 microfibril Anatomy 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
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- MJEMIOXXNCZZFK-UHFFFAOYSA-N ethylone Chemical compound CCNC(C)C(=O)C1=CC=C2OCOC2=C1 MJEMIOXXNCZZFK-UHFFFAOYSA-N 0.000 description 1
- 238000007730 finishing process Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
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- 238000011056 performance test Methods 0.000 description 1
- 125000005385 peroxodisulfate group Chemical group 0.000 description 1
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- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
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- 239000002994 raw material Substances 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical group [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
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- 238000005507 spraying Methods 0.000 description 1
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- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
本发明涉及一种采用硅溶胶制备抗皱棉织物的方法,包括:(1)将催化剂和硅酸盐先后溶解于去离子水中,然后在溶液中加入释酸剂,搅拌溶解,将棉织物浸入上述溶液,控制温度在10-30℃,持续1-48h后,两浸两轧,带液率80-85%,烘干后水洗,再烘干;(2)将上述棉织物浸入抗皱整理液中,浸渍3~5min,然后二浸二轧,带液率80-85%,最后烘干、焙烘即可。本发明制备得到的织物的拉伸断裂强力有显著的提高,对于目前抗皱整理织物的强力下降问题有明显改善,有广泛的应用前景和市场前景。The present invention relates to a method for preparing anti-wrinkle cotton fabric by using silica sol, comprising: (1) dissolving catalyst and silicate in deionized water successively, then adding an acid release agent into the solution, stirring to dissolve, and immersing the cotton fabric in the above-mentioned solution, control the temperature at 10-30°C, last for 1-48 hours, dip twice and roll twice, with a liquid retention rate of 80-85%, wash with water after drying, and then dry; (2) Immerse the above cotton fabric in the anti-wrinkle finishing solution , impregnated for 3 to 5 minutes, then dipped twice and rolled twice, with a liquid retention rate of 80-85%, and finally dried and baked. The tensile breaking strength of the fabric prepared by the invention is significantly improved, and the problem of strength decline of the current anti-wrinkle finishing fabric is obviously improved, and has wide application prospects and market prospects.
Description
技术领域technical field
本发明属于功能织物领域,特别涉及一种采用硅溶胶制备抗皱棉织物的方法。The invention belongs to the field of functional fabrics, in particular to a method for preparing wrinkle-resistant cotton fabrics by using silica sol.
背景技术Background technique
随着社会的发展与科技的进步,人们的物质生活日益丰富,现在人们已经不再满足于温饱,也开始追求丰富的精神文化。消费者对织物的选用要求也发生了改变,不仅仅局限于传统色彩艳丽的服饰,反而更注重服装的功能性、便捷性。由于棉织物具有穿着舒适,吸湿性好的特点,受到人们的喜爱,但其易起皱,不易护理,无法满足人们的日常需要。因此,对棉织物进行抗皱整理具有重要的现实意义。棉织物起皱的主要原因是棉纤维无定形区中分子链上的羟基在外力作用下能够发生滑移,在新的位置形成氢键而阻碍分子链回复到初始状态。目前,工业上主要采用2D树脂对棉织物进行抗皱整理,该方法有很好的抗皱效果,但整理后的织物释放甲醛的同时强力下降严重,即使对2D树脂进行醚化改性也无法避免甲醛的释放。随着环保要求的提高,无甲醛抗皱整理应运而生,使用最广泛的无甲醛抗皱整理剂为多元羧酸类整理剂,以BTCA整理效果最佳。2D树脂和多元羧酸类整理后的抗皱效果是由整理剂与棉纤维分子链上自由活动的羟基形成共价交联来实现。由于纤维素分子链间形成共价交联,与未整理的织物相比,各基本结构单元间的移动性受到限制,负担外力的情况更不均匀,会引起织物的强力下降,无法满足消费者的需求,提高抗皱整理织物的强力具有现实意义。With the development of society and the advancement of science and technology, people's material life is becoming more and more abundant. Now people are no longer satisfied with food and clothing, but also begin to pursue rich spiritual culture. Consumers' requirements for the selection of fabrics have also changed. They are not limited to traditional colorful clothing, but pay more attention to the functionality and convenience of clothing. Because cotton fabric has the characteristics of comfortable wearing and good hygroscopicity, it is liked by people, but it is easy to wrinkle and difficult to care, so it cannot meet people's daily needs. Therefore, the anti-wrinkle finishing of cotton fabric has important practical significance. The main reason for the wrinkling of cotton fabrics is that the hydroxyl groups on the molecular chains in the amorphous region of cotton fibers can slip under the action of external force, and form hydrogen bonds in new positions to prevent the molecular chains from returning to their original state. At present, 2D resins are mainly used in the industry for anti-wrinkle finishing of cotton fabrics. This method has a good anti-wrinkle effect, but the strength of the finished fabrics is severely reduced when the formaldehyde is released. Even if the 2D resin is modified by etherification, formaldehyde cannot be avoided. release. With the improvement of environmental protection requirements, formaldehyde-free anti-wrinkle finishing has emerged at the historic moment. The most widely used formaldehyde-free anti-wrinkle finishing agent is polycarboxylic acid finishing agent, and BTCA has the best finishing effect. The anti-wrinkle effect after finishing with 2D resin and polycarboxylic acid is realized by the formation of covalent cross-links between the finishing agent and the freely movable hydroxyl groups on the cotton fiber molecular chain. Due to the formation of covalent crosslinks between the cellulose molecular chains, compared with unfinished fabrics, the mobility between the basic structural units is limited, and the external force is more uneven, which will cause the strength of the fabric to decrease, which cannot satisfy consumers. It is of practical significance to improve the strength of anti-wrinkle finishing fabrics.
溶胶-凝胶法是用含高化学活性组分的化合物作为前驱体,在液相下将这些原料均匀混合,并进行水解、缩合化学反应,在溶液中形成稳定的透明溶胶体系,溶胶经陈化胶粒间缓慢聚合,形成三维空间网络结构的凝胶,凝胶经过干燥、烧结固化制备出分子乃至纳米亚结构的材料。不同种类溶胶可以通过浸涂、喷涂或连续涂层等方式用于纺织品的整理。目前,织物多是通过浸轧来涂层,然后在一定条件下干燥,在纺织品表面形成一层薄而透明的金属或硅氧化物薄膜,通过对涂层进行物理或化学改性赋予织物多种性能。The sol-gel method uses compounds containing highly chemically active components as precursors, uniformly mixes these raw materials in the liquid phase, and undergoes hydrolysis and condensation chemical reactions to form a stable transparent sol system in the solution. Slowly polymerize among the colloidal particles to form a gel with a three-dimensional space network structure. The gel is dried, sintered and solidified to prepare molecular and even nano-substructure materials. Different types of sols can be used for finishing textiles by dipping, spraying or continuous coating. At present, fabrics are mostly coated by padding, and then dried under certain conditions to form a thin and transparent metal or silicon oxide film on the surface of the textile. performance.
由于棉织物的孔径在10nm左右,直接将织物浸轧溶胶,大颗粒的溶胶难以进入到棉纤维微孔内部,容易洗去;织物浸渍溶液后烘干时,渗入微孔中的溶液随水分蒸发向外移动,也在微原纤或纤维之间形成凝胶,而在棉纤维的孔道内也难以存在。而低温下将棉织物浸入到含有释酸剂的硅酸盐溶液中,随时间的延长,释酸剂水解释放出酸从而降低溶液的pH值,溶液中硅酸盐分子均匀分布,纤维微孔内部的硅酸盐小分子也慢慢缩聚长大,进而形成溶胶而固定在纤维孔道内部,烘干后无法出来,沉积于纤维微孔或微纤间的凝胶能够提高纤维或分子链间的摩擦力,进而提升织物的拉伸断裂强力,因此研究硅溶胶低温原位生长的方法对提高抗皱织物强力指明一个新方向。Since the pore size of the cotton fabric is about 10nm, if the fabric is directly dipped into the sol, it is difficult for the large-particle sol to enter the micropores of the cotton fiber and is easy to wash away; when the fabric is soaked in the solution and dried, the solution that penetrates into the micropores evaporates with the water Moving outward, gel is also formed between microfibrils or fibers, and it is difficult to exist in the pores of cotton fibers. The cotton fabric is immersed in the silicate solution containing the acid-releasing agent at low temperature. As time goes by, the acid-releasing agent is hydrolyzed to release the acid, thereby reducing the pH value of the solution. The silicate molecules in the solution are evenly distributed, and the fibers are microporous. The small silicate molecules inside also slowly condense and grow up, and then form a sol and fix it inside the fiber channel, which cannot come out after drying. The gel deposited between the fiber micropores or microfibrils can improve the bonding between fibers or molecular chains. Therefore, the method of studying the low-temperature in-situ growth of silica sol points out a new direction for improving the strength of wrinkle-resistant fabrics.
发明内容Contents of the invention
本发明所要解决的技术问题是提供一种采用硅溶胶制备抗皱棉织物的方法,该方法制备得到的织物的拉伸断裂强力有显著的提高,对于目前抗皱整理织物的强力下降问题有明显改善,有广泛的应用前景和市场前景。The technical problem to be solved by the present invention is to provide a method for preparing wrinkle-resistant cotton fabrics by using silica sol, the tensile breaking strength of the fabrics prepared by this method is significantly improved, and the problem of strength decline of current wrinkle-resistant finishing fabrics is significantly improved. It has broad application prospect and market prospect.
本发明的一种采用硅溶胶制备抗皱棉织物的方法,包括:A kind of method adopting silica sol to prepare wrinkle-resistant cotton fabric of the present invention comprises:
(1)将催化剂和硅酸盐先后溶解于去离子水中,然后在溶液中加入释酸剂,搅拌溶解,将棉织物浸入上述溶液,控制温度在10-30℃,持续1-48h后,两浸两轧,带液率80-85%,烘干后水洗,再烘干;其中,硅酸盐用量为溶液质量的1-5%,催化剂与硅酸盐的摩尔比值为0-0.5,释酸剂用量为溶液质量的1-4%;(1) Dissolve the catalyst and the silicate in deionized water successively, then add an acid release agent into the solution, stir to dissolve, immerse the cotton fabric in the above solution, control the temperature at 10-30°C for 1-48 hours, and then Dipping and rolling, the liquid rate is 80-85%, washed with water after drying, and then dried; wherein, the amount of silicate is 1-5% of the solution mass, and the molar ratio of catalyst to silicate is 0-0.5. The amount of acid agent is 1-4% of the solution mass;
(2)将上述棉织物浸入抗皱整理液中,浸渍3~5min,然后二浸二轧,带液率80-85%,最后烘干、焙烘即可。(2) Immerse the above-mentioned cotton fabric in the anti-wrinkle finishing solution for 3-5 minutes, then soak twice and roll twice, with a liquid retention rate of 80-85%, and finally dry and bake.
所述步骤(1)中的催化剂为硫酸铵、醋酸中的一种;硅酸盐为硅酸钠;释酸剂为DL-泛酰内酯、葡糖酸内酯、单乙酸甘油酯、乙二醇二乙酸酯中的一种。The catalyst in the step (1) is one of ammonium sulfate and acetic acid; the silicate is sodium silicate; the acid release agent is DL-panthenolactone, gluconolactone, glycerol monoacetate, ethyl One of the glycol diacetates.
所述步骤(1)中的烘干方式为热定型机上烘干,烘干温度为80-120℃,烘干时间为1-3min。The drying method in the step (1) is drying on a heat setting machine, the drying temperature is 80-120° C., and the drying time is 1-3 minutes.
所述步骤(1)中的水洗方式为常温水洗机水洗,水洗时间为5-30min。The washing method in the step (1) is machine washing at room temperature, and the washing time is 5-30 minutes.
所述步骤(2)中的抗皱整理液的组成包括:抗皱整理剂、催化剂、引发剂、强力保护剂以及水;其中,抗皱整理剂为整理液质量的3-9%,引发剂为抗皱整理剂质量的0-1.5%,催化剂与抗皱整理剂的摩尔比为1:2-2:1,强力保护剂为整理液质量的0-2%,余量为水。The composition of the anti-wrinkle finishing liquid in the step (2) includes: anti-wrinkle finishing agent, catalyst, initiator, strong protective agent and water; wherein, the anti-wrinkle finishing agent is 3-9% of the mass of the finishing liquid, and the initiator is anti-wrinkle finishing 0-1.5% of the mass of the finishing agent, the molar ratio of the catalyst to the anti-wrinkle finishing agent is 1:2-2:1, the strong protective agent is 0-2% of the mass of the finishing liquid, and the balance is water.
所述抗皱整理剂为多元羧酸类抗皱整理剂;所述催化剂为次亚磷酸钠、磷酸氢二钠、磷酸二氢钠中的一种;所述引发剂为过二硫酸钠或过二硫酸钾;所述强力保护剂为三乙醇胺。The anti-wrinkle finishing agent is polycarboxylic acid anti-wrinkle finishing agent; the catalyst is one of sodium hypophosphite, disodium hydrogen phosphate, and sodium dihydrogen phosphate; the initiator is sodium peroxodisulfate or peroxodisulfate Potassium; The strong protective agent is triethanolamine.
所述多元羧酸类抗皱整理剂为马来酸MA、衣康酸IA、丁烷四羧酸BTCA、柠檬酸CA中的一种或两种。The polycarboxylic acid anti-wrinkle finishing agent is one or two of maleic acid MA, itaconic acid IA, butane tetracarboxylic acid BTCA, and citric acid CA.
所述步骤(2)中的烘干方式为热定型机上烘干,烘干温度为80-100℃,烘干时间为3-10min。The drying method in the step (2) is drying on a heat setting machine, the drying temperature is 80-100° C., and the drying time is 3-10 minutes.
所述步骤(2)中的焙烘温度为160-180℃,焙烘时间为1-3min。The baking temperature in the step (2) is 160-180° C., and the baking time is 1-3 minutes.
本发明将硅溶胶低温原位生长与抗皱整理两步进行,首先低温条件下将棉织物浸渍于硅酸盐、催化剂和释酸剂的混合溶液中,pH较高时,混合溶液为小分子,由于棉纤维的孔径在10nm左右,小分子能够均匀的分布于棉纤维的微孔和微纤之间,随着释酸剂的水解,混合液的pH逐渐降低,当达到形成溶胶的条件时,小分子发生缩聚反应,形成溶胶而沉积于棉织物的微纤间或微孔中,烘干后能够沉积于微纤间或微孔中,水洗后不易除去,从而阻碍了棉纤维或分子链的滑移,进而增强了织物的拉伸断裂强力,进一步进行抗皱整理所得织物与单独进行抗皱整理的织物相比,拉伸断裂强力明显提高。采用这种物理与化学相结合的方法处理棉织物,得到的织物拉伸断裂强力比单独整理棉织物的强力高,几乎不影响折皱回复角。In the present invention, low-temperature in-situ growth of silica sol and anti-wrinkle finishing are performed in two steps. First, the cotton fabric is immersed in a mixed solution of silicate, catalyst and acid release agent under low temperature conditions. When the pH is high, the mixed solution is a small molecule. Because the pore size of cotton fiber is about 10nm, small molecules can be evenly distributed between the micropores and microfibers of cotton fiber. With the hydrolysis of the acid release agent, the pH of the mixed solution gradually decreases. When the conditions for forming a sol are reached, Small molecules undergo polycondensation reaction to form sol and deposit in the microfibers or micropores of cotton fabrics. After drying, they can deposit in the microfibers or micropores, and are not easy to remove after washing, thus hindering the slippage of cotton fibers or molecular chains. , which in turn enhances the tensile breaking strength of the fabric, and the tensile breaking strength of the fabric obtained by further anti-wrinkle finishing is significantly improved compared with the fabric which is individually anti-wrinkle finishing. Using this physical and chemical method to treat cotton fabrics, the tensile breaking strength of the obtained fabrics is higher than that of cotton fabrics treated alone, and the wrinkle recovery angle is hardly affected.
有益效果Beneficial effect
(1)本发明与传统抗皱整理工艺相比,制备方法简单,成本低,不增加能耗,便于工业化生产;(1) Compared with the traditional anti-wrinkle finishing process, the present invention has simple preparation method, low cost, no increase in energy consumption, and is convenient for industrial production;
(2)本发明中胶粒由小分子缩聚变大而固定于棉纤维之间或纤维的微孔结构中,该固着方式能够与纤维紧密结合,使得整理效果更持久也更耐洗涤;(2) In the present invention, the colloidal particles are condensed from small molecules to become larger and fixed between the cotton fibers or in the microporous structure of the fibers. This fixation method can be closely combined with the fibers, making the finishing effect longer and more resistant to washing;
(3)本发明制备得到的织物的拉伸断裂强力有显著的提高,对于目前抗皱整理织物的强力下降问题有明显改善,有广泛的应用前景和市场前景。(3) The tensile breaking strength of the fabric prepared by the present invention is significantly improved, and the strength drop problem of the current anti-wrinkle finishing fabric is significantly improved, and has wide application prospects and market prospects.
具体实施方式Detailed ways
下面结合具体实施例,进一步阐述本发明。应理解,这些实施例仅用于说明本发明而不用于限制本发明的范围。此外应理解,在阅读了本发明讲授的内容之后,本领域技术人员可以对本发明作各种改动或修改,这些等价形式同样落于本申请所附权利要求书所限定的范围。Below in conjunction with specific embodiment, further illustrate the present invention. It should be understood that these examples are only used to illustrate the present invention and are not intended to limit the scope of the present invention. In addition, it should be understood that after reading the teachings of the present invention, those skilled in the art can make various changes or modifications to the present invention, and these equivalent forms also fall within the scope defined by the appended claims of the present application.
实施例1Example 1
将2.164g催化剂(NH4)2SO4、9.32g的Na2SiO3·9H2O先后溶解于200mL去离子水中,然后在溶液中加入6g释酸剂DL-泛酰内酯,迅速搅拌溶解,将棉织物浸入上述溶液,控制温度在18℃,持续24h后,两浸两轧,带液率80%,80℃烘干3min后水洗10min,再80℃烘干3min;Dissolve 2.164g of catalyst (NH 4 ) 2 SO 4 and 9.32g of Na 2 SiO 3 9H 2 O in 200mL of deionized water, then add 6g of acid release agent DL-pantothenolactone into the solution, stir rapidly to dissolve , soak the cotton fabric in the above solution, control the temperature at 18°C, continue for 24 hours, dip and roll twice, the liquid retention rate is 80%, dry at 80°C for 3 minutes, wash with water for 10 minutes, and then dry at 80°C for 3 minutes;
将上述棉织物和未处理的棉织物均浸入抗皱整理液中,浸渍3min,然后二浸二轧,带液率为85%,100℃烘干10min,然后180℃焙烘1.5min。抗皱整理液包含有:质量分数为6%的MA-IA抗皱整理剂及次亚磷酸钠,过二硫酸钾和三乙醇胺,余量为去离子水。其中MA与IA的摩尔比为1:1,次亚磷酸钠与MA和IA之和的摩尔比为1:1,过二硫酸钾为抗皱整理剂质量的1.5%,三乙醇胺为整理液质量的2%。Both the above-mentioned cotton fabrics and untreated cotton fabrics were immersed in the anti-wrinkle finishing solution for 3 minutes, then dipped and rolled twice, the liquid retention rate was 85%, dried at 100°C for 10 minutes, and then baked at 180°C for 1.5 minutes. The anti-wrinkle finishing solution includes: MA-IA anti-wrinkle finishing agent with a mass fraction of 6%, sodium hypophosphite, potassium peroxodisulfate and triethanolamine, and the balance is deionized water. Wherein the mol ratio of MA and IA is 1:1, the mol ratio of sodium hypophosphite and the sum of MA and IA is 1:1, potassium peroxodisulfate is 1.5% of the anti-wrinkle finishing agent quality, and triethanolamine is 1% of the finishing liquid quality 2%.
实施例2Example 2
将9.32g Na2SiO3·9H2O溶解于200mL去离子水中,然后在溶液中加入6g释酸剂DL-泛酰内酯,迅速搅拌溶解,将棉织物浸入上述溶液,控制温度在22℃,持续24h后,两浸两轧,带液率80%,80℃烘干3min后水洗10min,再烘干3min;Dissolve 9.32g Na 2 SiO 3 ·9H 2 O in 200mL of deionized water, then add 6g of acid release agent DL-pantothenolactone into the solution, stir rapidly to dissolve, immerse the cotton fabric in the above solution, and control the temperature at 22°C , after 24 hours, double dipping and rolling, the liquid retention rate is 80%, dry at 80°C for 3 minutes, wash with water for 10 minutes, and then dry for 3 minutes;
将上述棉织物和未处理的棉织物均浸入抗皱整理液中,浸渍3min,然后二浸二轧,带液率为85%,100℃烘干10min,然后180℃焙烘1.5min。抗皱整理液包含有:质量分数为8%的MA-IA抗皱整理剂及次亚磷酸钠,过二硫酸钾和三乙醇胺,余量为去离子水。其中MA与IA的摩尔比为1:1,次亚磷酸钠与MA和IA之和的摩尔比为1:1,过二硫酸钾为抗皱整理剂质量的1.5%,三乙醇胺为整理液质量的2%。Both the above-mentioned cotton fabrics and untreated cotton fabrics were immersed in the anti-wrinkle finishing solution for 3 minutes, then dipped and rolled twice, the liquid retention rate was 85%, dried at 100°C for 10 minutes, and then baked at 180°C for 1.5 minutes. The anti-wrinkle finishing solution includes: MA-IA anti-wrinkle finishing agent with a mass fraction of 8%, sodium hypophosphite, potassium peroxodisulfate and triethanolamine, and the balance is deionized water. Wherein the mol ratio of MA and IA is 1:1, the mol ratio of sodium hypophosphite and the sum of MA and IA is 1:1, potassium peroxodisulfate is 1.5% of the anti-wrinkle finishing agent quality, and triethanolamine is 1% of the finishing liquid quality 2%.
实施例3Example 3
将9.32g Na2SiO3·9H2O溶解于200mL去离子水中,然后在溶液中加入6g释酸剂DL-泛酰内酯,迅速搅拌溶解,将棉织物浸入上述溶液,控制温度在20℃,持续24h后,两浸两轧,带液率80%,80℃烘干3min后水洗10min,再烘干3min;Dissolve 9.32g Na 2 SiO 3 ·9H 2 O in 200mL of deionized water, then add 6g of acid release agent DL-pantothenolactone into the solution, stir rapidly to dissolve, immerse the cotton fabric in the above solution, and control the temperature at 20°C , after 24 hours, double dipping and rolling, the liquid retention rate is 80%, dry at 80°C for 3 minutes, wash with water for 10 minutes, and then dry for 3 minutes;
将上述棉织物和未处理的棉织物均浸入抗皱整理液中,浸渍5min,然后二浸二轧,带液率为85%,80℃烘干3min,然后180℃焙烘1.5min。抗皱整理液包含有:质量分数为4%的BTCA抗皱整理剂及次亚磷酸钠,其中次亚磷酸钠与BTCA的摩尔比为1:1,三乙醇胺为整理液质量的2%,余量为去离子水。Both the above-mentioned cotton fabric and the untreated cotton fabric were immersed in the anti-wrinkle finishing solution for 5 minutes, then dipped twice and rolled twice, with a liquid retention rate of 85%, dried at 80°C for 3 minutes, and then baked at 180°C for 1.5 minutes. The anti-wrinkle finishing solution contains: BTCA anti-wrinkle finishing agent with a mass fraction of 4% and sodium hypophosphite, wherein the molar ratio of sodium hypophosphite to BTCA is 1:1, triethanolamine is 2% of the mass of the finishing solution, and the balance is Deionized water.
整理得到的织物剪成试样在恒温恒湿室(温度21±1℃湿度为65±2%)平衡至少4小时,待测。对整理织物进行各项指标测试,具体如下:Cut the finished fabric into samples and equilibrate for at least 4 hours in a constant temperature and humidity room (temperature 21±1°C and humidity 65±2%) for at least 4 hours to be tested. Various index tests are carried out on the finished fabric, as follows:
抗皱性能测试参照AATCC66-2003标准在美国SDL公司的弹性回复仪上测试。The anti-wrinkle performance test is tested on the elastic recovery instrument of SDL company in the United States according to the AATCC66-2003 standard.
断裂强力测试参照GB3923.1-1997纺织品织物拉伸性能第1部分:断裂强力和断裂伸长率的测定。使用美国Tiniius Olsen公司H10KS型强力测试仪上测定。The breaking strength test refers to GB3923.1-1997 Textile Fabric Tensile Properties Part 1: Determination of breaking strength and elongation at break. It is measured on the H10KS strength tester of Tiniius Olsen Company in the United States.
表1 实施例1中硅溶胶整理前后织物的抗皱性能Table 1 The wrinkle resistance of fabrics before and after silica sol finishing in Example 1
表2 实施例2中硅溶胶整理前后织物的抗皱性能The wrinkle resistance of fabric before and after silica sol finishing in embodiment 2 in table 2
表3 实施例3中硅溶胶整理前后织物的抗皱性能Table 3 The wrinkle resistance of fabrics before and after silica sol finishing in embodiment 3
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