CN105274844B - A method for improving the formulation of adhesive for sizing by utilizing polyurethane and ethylene glycol phenyl ether - Google Patents
A method for improving the formulation of adhesive for sizing by utilizing polyurethane and ethylene glycol phenyl ether Download PDFInfo
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- 229920002635 polyurethane Polymers 0.000 title claims abstract description 55
- 239000004814 polyurethane Substances 0.000 title claims abstract description 55
- 239000000853 adhesive Substances 0.000 title claims abstract description 48
- 230000001070 adhesive effect Effects 0.000 title claims abstract description 48
- 238000004513 sizing Methods 0.000 title claims abstract description 47
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 title claims abstract description 35
- 238000000034 method Methods 0.000 title claims abstract description 20
- 239000000203 mixture Substances 0.000 title description 4
- 238000009472 formulation Methods 0.000 title description 3
- 229920002472 Starch Polymers 0.000 claims abstract description 60
- 239000008107 starch Substances 0.000 claims abstract description 60
- 235000019698 starch Nutrition 0.000 claims abstract description 60
- 229910019142 PO4 Inorganic materials 0.000 claims abstract description 43
- 239000010452 phosphate Substances 0.000 claims abstract description 43
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 39
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims abstract description 36
- -1 phosphate ester Chemical class 0.000 claims abstract description 13
- 238000002156 mixing Methods 0.000 claims abstract description 4
- 238000003756 stirring Methods 0.000 claims description 27
- AEDZKIACDBYJLQ-UHFFFAOYSA-N ethane-1,2-diol;hydrate Chemical compound O.OCCO AEDZKIACDBYJLQ-UHFFFAOYSA-N 0.000 claims description 13
- 238000010438 heat treatment Methods 0.000 claims description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims 2
- 238000009413 insulation Methods 0.000 claims 2
- 229910021529 ammonia Inorganic materials 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 239000007787 solid Substances 0.000 abstract description 5
- 239000004753 textile Substances 0.000 abstract description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract description 3
- 230000035699 permeability Effects 0.000 abstract 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 28
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 15
- 239000002002 slurry Substances 0.000 description 10
- 239000000243 solution Substances 0.000 description 9
- 239000000835 fiber Substances 0.000 description 7
- 229920000742 Cotton Polymers 0.000 description 6
- 239000011230 binding agent Substances 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- 239000011259 mixed solution Substances 0.000 description 4
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 4
- 238000004321 preservation Methods 0.000 description 4
- 206010020112 Hirsutism Diseases 0.000 description 3
- 239000004372 Polyvinyl alcohol Substances 0.000 description 3
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229920000058 polyacrylate Polymers 0.000 description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 description 3
- OMIHGPLIXGGMJB-UHFFFAOYSA-N 7-oxabicyclo[4.1.0]hepta-1,3,5-triene Chemical compound C1=CC=C2OC2=C1 OMIHGPLIXGGMJB-UHFFFAOYSA-N 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Chemical group CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- 239000011268 mixed slurry Substances 0.000 description 2
- 238000009941 weaving Methods 0.000 description 2
- 229920002125 Sokalan® Polymers 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000009990 desizing Methods 0.000 description 1
- 239000001245 distarch phosphate Substances 0.000 description 1
- 235000013804 distarch phosphate Nutrition 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000033001 locomotion Effects 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
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- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Description
技术领域technical field
本发明涉及一种利用聚氨酯和乙二醇苯醚改善浆纱用粘合剂配方的方法,属于纺织加工技术领域。The invention relates to a method for improving the formula of an adhesive for sizing by using polyurethane and ethylene glycol phenyl ether, which belongs to the technical field of textile processing.
背景技术Background technique
织造时,经纱由经轴到织口过程中在综框的作用会产生4000次左右的往复运动。在此过程中,作为保护经纱性能的粘合剂所发挥的作用是增加强力,减少毛羽等。纺织加工行业常用的三大粘合剂的种类是:淀粉类,丙烯酸类和聚乙烯醇类。粘合剂的性能对浸轧粘合剂后经纱的性能起重要作用。因此,为了保护经纱,对经纱进行浸轧粘合剂,粘合剂对经纱的保护主要从两个方面:一是粘合剂浸透进入纱线内部,增加纤维之间的抱合力,形成浸透层,提高经纱的断裂强力和伸长率;二是粘合剂在纱线表面进行包覆,包覆毛羽,形成被覆层,提高经纱的耐磨性。如中国公开出版物《高分子材料科学与工程》,公开日期2009年8月,文章名称为磷酸酯淀粉/聚丙烯酸酯共混膜的织态结构与性能,该文献介绍了通过对磷酸酯淀粉辅以聚丙烯酸酯浆料,以提高浆膜的柔韧性,其不足之处是仅对磷酸酯淀粉辅以丙聚烯酸酯来改善浆膜的柔韧性仍然不能很好的满足织造时对经纱表面浆膜柔韧性的要求,如中国公开出版物《棉纺织技术》,公开日期2010年11月,文章名称为马来酸酐酯化丙烯酸酯接枝淀粉浆料的研究,该文献介绍了一种利用马来酸酐酯化丙烯酸酯接枝淀粉以改善浆膜柔韧性的方法,其不足之处是此淀粉接枝工艺流程长,耗时较多,能耗高,如中国专利公开号CN102329437A,公开日2012年01月25日,发明创造的名称为一种可降解淀粉复合浆料,该申请案公开了采用植物淀粉、乙酰化二淀粉磷酸酯、聚丙烯酸、淀粉和PVA复配的一种浆料,其不足之处是虽然使得浆膜的韧性增加,但是PVA退浆后不能快速降解,污染环境。如中国公开出版物《棉纺织技术》,公开日期2012年7月,文章名称为水性聚氨酯对淀粉浆料的改性作用,该文献说明了在淀粉浆料中加入水性聚氨酯组分,可使粘着力提高,并改善浆膜的力学性能,其不足之处为加水性聚氨酯对浆膜性能的改善仍不能很好的满足浆料对纱线的粘附性。中国专利公开号CN103923297A,公开日2014年07月16日,发明创造的名称为一种用于增韧淀粉浆膜的水性聚氨酯及其制备方法和应用,该申请案公开了合成适用于淀粉浆料增韧的聚氨酯合成方法,解决了淀粉上浆成膜后出现浆膜硬脆的特点,由于使用了聚氨酯,提高了淀粉与聚氨酯的混合浆料对纤维的粘附性能,其不足在于公开的聚氨酯主要适用对象是酸解淀粉,并且该技术方案中淀粉与聚氨酯的混合浆料的粘附性能提高幅度较小。During weaving, the effect of the warp yarn on the heald frame will produce about 4000 reciprocating motions during the process from the warp beam to the fell. In this process, the role of the binder that protects the performance of the warp is to increase the strength and reduce hairiness. The three types of adhesives commonly used in the textile processing industry are: starch, acrylic and polyvinyl alcohol. The properties of the binder play an important role in the properties of the warp after padding the binder. Therefore, in order to protect the warp yarn, the warp yarn is padded with adhesive. The adhesive protects the warp yarn mainly from two aspects: one is that the adhesive penetrates into the yarn, increases the cohesion between fibers, and forms a soaked layer. , improve the breaking strength and elongation of the warp; the second is that the adhesive coats the surface of the yarn to cover the hairiness to form a coating layer and improve the wear resistance of the warp. Such as the Chinese publication "Macromolecular Materials Science and Engineering", the publication date is August 2009, the title of the article is the texture structure and performance of the phosphate starch/polyacrylate blend film. Supplemented with polyacrylate size to improve the flexibility of the size film, the disadvantage is that only phosphate starch supplemented with acrylic polyacrylate to improve the flexibility of the size film still cannot meet the requirements of the warp yarn during weaving. The requirements of surface size film flexibility, such as the Chinese publication "Cotton Textile Technology", the date of publication in November 2010, the title of the article is the study of maleic anhydride esterified acrylate grafted starch size, and this document introduces a The method of utilizing maleic anhydride to esterify acrylate grafted starch to improve the flexibility of the size film has the disadvantages that the starch grafting process is long, time-consuming, and energy-consuming, such as Chinese Patent Publication No. CN102329437A, disclosed On January 25, 2012, the name of the invention was a degradable starch composite slurry. The application disclosed a slurry compounded with plant starch, acetylated distarch phosphate, polyacrylic acid, starch and PVA. The disadvantage is that although the toughness of the size film is increased, the PVA cannot be degraded quickly after desizing and pollutes the environment. Such as China's public publication "Cotton Textile Technology", the publication date was July 2012, and the title of the article is the modification of water-based polyurethane to starch size. This document has explained that adding water-based polyurethane components to starch size can make adhesion The strength is improved and the mechanical properties of the size film are improved. The disadvantage is that the improvement of the performance of the size film by adding water-based polyurethane can not satisfy the adhesion of the size to the yarn. Chinese Patent Publication No. CN103923297A, published on July 16, 2014, the name of the invention is a kind of water-based polyurethane for toughening starch size film and its preparation method and application. The toughened polyurethane synthesis method solves the hard and brittle characteristics of the starch film after starch sizing and film formation. Due to the use of polyurethane, the adhesion performance of the mixed slurry of starch and polyurethane to fibers is improved. The disadvantage of the disclosed polyurethane is that it is mainly The applicable object is acid-thinned starch, and the adhesive performance of the mixed slurry of starch and polyurethane in this technical proposal is slightly improved.
发明内容Contents of the invention
针对上述存在的问题,本发明的目的在于提供一种利用聚氨酯和乙二醇苯醚改善浆纱用粘合剂配方的方法,为了实现上述目的,其技术解决方案为:For above-mentioned existing problem, the object of the present invention is to provide a kind of method that utilizes polyurethane and ethylene glycol phenyl ether to improve the adhesive formula for sizing, in order to realize above-mentioned purpose, its technical solution is:
一种利用聚氨酯和乙二醇苯醚改善浆纱用粘合剂配方的方法,包括由磷酸酯淀粉、丙烯酸酯和水组份组成的浆纱用粘合剂配方以及经接通电源搅拌并加热,加热温度范围是95-100℃,加热的时间是1小时,其中包含两个步骤:第一步是搅拌,搅拌的时间为20分钟;第二步是保温,保温的时间为40分钟。搅拌速度范围是200-400转/分钟制成的浆纱用粘合剂,所述的方法是指在磷酸酯淀粉、丙烯酸酯和水的浆纱用粘合剂配方中添加聚氨酯和乙二醇苯醚,其中,磷酸酯淀粉质量是磷酸酯淀粉、丙烯酸酯、聚氨酯、乙二醇苯醚和水总质量的3-5%,丙烯酸酯质量是磷酸酯淀粉、丙烯酸酯、聚氨酯、乙二醇苯醚和水总质量的3-5%,聚氨酯质量是磷酸酯淀粉、丙烯酸酯、聚氨酯、乙二醇苯醚和水总质量的0.1-1%,乙二醇苯醚质量是磷酸酯淀粉、丙烯酸酯、聚氨酯、乙二醇苯醚和水总质量的0.1-2%。A method for improving the adhesive formula for sizing by utilizing polyurethane and ethylene glycol phenyl ether, comprising the adhesive formula for sizing composed of phosphate starch, acrylate and water components and stirring and heating after turning on the power supply , the heating temperature range is 95-100°C, and the heating time is 1 hour, which includes two steps: the first step is stirring, and the stirring time is 20 minutes; the second step is heat preservation, and the heat preservation time is 40 minutes. The range of agitation speed is 200-400 rev/min to make the adhesive for sizing, said method refers to adding polyurethane and ethylene glycol in the adhesive formulation for sizing of phosphate starch, acrylate and water Phenyl ether, wherein, the quality of phosphate starch is 3-5% of the total mass of phosphate starch, acrylate, polyurethane, ethylene glycol phenyl ether and water, and the quality of acrylate is phosphate starch, acrylate, polyurethane, ethylene glycol 3-5% of the total mass of phenylene ether and water, the mass of polyurethane is 0.1-1% of the total mass of phosphate starch, acrylate, polyurethane, ethylene glycol phenyl ether and water, the mass of ethylene glycol phenyl ether is phosphate starch, 0.1-2% of the total mass of acrylate, polyurethane, ethylene glycol phenyl ether and water.
所述的聚氨酯为可生物降解的水性聚氨酯。The polyurethane is biodegradable waterborne polyurethane.
由于采用了以上技术方案,在浆纱用粘合剂中加入的乙二醇苯醚分子结构中有羟基和醚键,对磷酸酯淀粉与丙烯酸酯均具有良好的亲和能力。乙二醇苯醚中的醚键与磷酸酯淀粉中的酯键以及丙烯酸酯中的酯键形成氢键,乙二醇苯醚中的羟基与磷酸酯淀粉的羟基也可形成氢键。通过乙二醇苯醚形成氢键可以使得磷酸酯淀粉分子与丙烯酸酯的分子在溶液中可以更好地相互溶合,粘合剂的液体形成的膜结构优化,粘度稳定。而聚氨酯具有良好的粘结性能,能够将纱线内部的纤维粘结起来。聚氨酯主要实现链接磷酸酯淀粉和纤维之间以及聚氨酯与纤维之间的粘附性能,由于聚氨酯中的酯键与磷酸酯淀粉中的酯键具有非常好的作用力,从而比它与单纯的原淀粉或酸解淀粉具有更好的亲和力,从而本技术方案提高浆纱用粘合剂的原理并非简单的聚氨酯与磷酸酯淀粉的简单混合,而是利用酯键间形成的氢键作用、乙二醇苯醚中的羟基与磷酸酯淀粉的羟基也可形成氢键以及磷酸酯淀粉、乙二醇苯醚和聚氨酯对纤维的作用共同相互作用而实现的效果,最终实现上将用粘合剂更好的上浆效果。浆纱用粘合剂在纱线上的分布形式分为两种,即被覆与浸透,浸透率显示出浆纱用粘合剂进入纱线内部的能力,被覆率反映了浆纱用粘合剂对纱线的保护性能。经本工艺处理后的浆纱用粘合剂能够很好的增加了纤维之间的抱合力,提高了纱线的强力和保伸性。在处理纱线过程中,能够更好的包裹在纱线的表面,从而提高纱线的被覆率。在纱线相互摩擦过程中能更好的保护纱线的表面毛羽。Due to the adoption of the above technical scheme, the molecular structure of ethylene glycol phenyl ether added to the adhesive for sizing has hydroxyl groups and ether bonds, and has good affinity for phosphate starch and acrylate. The ether bonds in ethylene glycol phenyl ether form hydrogen bonds with the ester bonds in phosphate starch and the ester bonds in acrylate, and the hydroxyl groups in ethylene glycol phenyl ether and the hydroxyl groups of phosphate starch can also form hydrogen bonds. The hydrogen bond formed by the ethylene glycol phenyl ether can make the phosphate ester starch molecules and the acrylate molecules can be better blended in the solution, and the film structure formed by the liquid of the adhesive is optimized and the viscosity is stable. Polyurethane has good bonding properties and can bond the fibers inside the yarn. Polyurethane mainly realizes the adhesion between phosphate starch and fiber and between polyurethane and fiber. Since the ester bond in polyurethane and the ester bond in phosphate starch have a very good force, it is better than that of simple raw material. Starch or acid-thinned starch has better affinity, so the principle of improving the adhesive for sizing in this technical scheme is not a simple mixing of polyurethane and phosphate starch, but the use of hydrogen bonds formed between ester bonds, ethylene glycol The hydroxyl group in the alcohol phenyl ether and the hydroxyl group of the phosphate starch can also form a hydrogen bond and the interaction between the phosphate starch, ethylene glycol phenyl ether and polyurethane on the fiber, and finally achieve the effect of using the adhesive more Good sizing effect. The distribution form of sizing adhesive on the yarn is divided into two types, that is, coating and impregnation. The penetration rate shows the ability of the sizing adhesive to enter the interior of the yarn, and the coverage reflects the ability of the sizing adhesive to penetrate into the yarn. Protective properties for yarns. The binder for sizing treated by the process can well increase the cohesion force between fibers and improve the strength and stretch retention of yarn. In the process of processing the yarn, it can better wrap the surface of the yarn, thereby improving the coverage of the yarn. The surface hairiness of the yarn can be better protected during the friction between the yarns.
具体实施方式detailed description
一种利用聚氨酯和乙二醇苯醚改善浆纱用粘合剂配方的方法,包括由磷酸酯淀粉、丙烯酸酯和水组份组成的浆纱用粘合剂配方以及经接通电源搅拌并加热,加热温度范围是95-100℃,加热的时间是1小时,其中包含两个步骤:第一步是搅拌,搅拌的时间为20分钟;第二步是保温,保温的时间为40分钟。搅拌速度范围是200-400转/分钟制成的浆纱用粘合剂,所述的方法是指在磷酸酯淀粉、丙烯酸酯和水的浆纱用粘合剂配方中添加聚氨酯和乙二醇苯醚,其中,磷酸酯淀粉质量是磷酸酯淀粉、丙烯酸酯、聚氨酯、乙二醇苯醚和水总质量的3-5%,丙烯酸酯质量是磷酸酯淀粉、丙烯酸酯、聚氨酯、乙二醇苯醚和水总质量的3-5%,聚氨酯质量是磷酸酯淀粉、丙烯酸酯、聚氨酯、乙二醇苯醚和水总质量的0.1-1%,乙二醇苯醚质量是磷酸酯淀粉、丙烯酸酯、聚氨酯、乙二醇苯醚和水总质量的0.1-2%。A method for improving the adhesive formula for sizing by utilizing polyurethane and ethylene glycol phenyl ether, comprising the adhesive formula for sizing composed of phosphate starch, acrylate and water components and stirring and heating after turning on the power supply , the heating temperature range is 95-100°C, and the heating time is 1 hour, which includes two steps: the first step is stirring, and the stirring time is 20 minutes; the second step is heat preservation, and the heat preservation time is 40 minutes. The range of agitation speed is 200-400 rev/min to make the adhesive for sizing, said method refers to adding polyurethane and ethylene glycol in the adhesive formulation for sizing of phosphate starch, acrylate and water Phenyl ether, wherein, the quality of phosphate starch is 3-5% of the total mass of phosphate starch, acrylate, polyurethane, ethylene glycol phenyl ether and water, and the quality of acrylate is phosphate starch, acrylate, polyurethane, ethylene glycol 3-5% of the total mass of phenylene ether and water, the mass of polyurethane is 0.1-1% of the total mass of phosphate starch, acrylate, polyurethane, ethylene glycol phenyl ether and water, the mass of ethylene glycol phenyl ether is phosphate starch, 0.1-2% of the total mass of acrylate, polyurethane, ethylene glycol phenyl ether and water.
所述的聚氨酯为可生物降解的水性聚氨酯。The polyurethane is biodegradable waterborne polyurethane.
按上述方法。Follow the above method.
实施例1Example 1
用电子天枰准确称量30g磷酸酯淀粉和30g丙烯酸酯固体浆料置于1L容器底部,同时称取1g的聚氨酯和1g的乙二醇苯醚加入容器,往容器中加水,使磷酸酯淀粉,丙烯酸酯,聚氨酯,乙二醇苯醚和水的总重量达到1kg,将溶液搅拌均匀,将容器置于100℃水浴锅中加热,同时使用搅拌器对容器中的混合液进行搅拌,搅拌速度设定为300转/分钟,搅拌20分钟,当粘合剂完全糊化之后,停止搅拌,用薄膜将容器密封,继续在95-100℃的水浴锅中煮浆40分钟。制备成改善后的浆纱用粘合剂,之后将准备好的棉粗纱绕在特制的浆纱架上,将浆纱架浸没的粘合剂中进行上浆,5分钟后取出,置于80℃烘箱中烘干30分钟。Accurately weigh 30g of phosphate starch and 30g of acrylate solid slurry with an electronic balance and place them at the bottom of a 1L container. At the same time, weigh 1g of polyurethane and 1g of ethylene glycol phenyl ether into the container, add water to the container, and make the phosphate starch , the total weight of acrylate, polyurethane, ethylene glycol phenyl ether and water reaches 1kg, stir the solution evenly, heat the container in a water bath at 100°C, and use a stirrer to stir the mixed solution in the container at the same time, the stirring speed Set at 300 rpm, stir for 20 minutes, stop stirring when the adhesive is completely gelatinized, seal the container with a film, and continue to cook the slurry in a water bath at 95-100°C for 40 minutes. Prepare an improved sizing adhesive, wind the prepared cotton roving on a special sizing frame, immerse the sizing frame in the adhesive for sizing, take it out after 5 minutes, and place it at 80°C Dry in the oven for 30 minutes.
实施例2Example 2
用电子天枰准确称量50g磷酸酯淀粉和50g丙烯酸酯固体浆料置于1L容器底部,同时称取10g的聚氨酯和20g的乙二醇苯醚溶液加入容器,往容器中加水,使磷酸酯淀粉,丙烯酸酯,聚氨酯,乙二醇苯醚和水的总重量达到1kg,将溶液搅拌均匀,将容器置于100℃水浴锅中加热,同时使用搅拌器对容器中的混合液进行搅拌,搅拌速度设定为300转/分钟,搅拌20分钟,当粘合剂完全糊化之后,停止搅拌,用薄膜将容器密封,继续在95-100℃的水浴锅中煮浆40分钟。制备成改善后的浆纱用粘合剂,之后将准备好的棉粗纱绕在特制的浆纱架上,将浆纱架浸没的粘合剂中进行上浆,5分钟后取出,置于80℃烘箱中烘干30分钟。Accurately weigh 50g of phosphate starch and 50g of acrylate solid slurry with an electronic balance and place them at the bottom of a 1L container. At the same time, weigh 10g of polyurethane and 20g of ethylene glycol phenyl ether solution into the container, add water to the container, and make the phosphate The total weight of starch, acrylate, polyurethane, ethylene glycol phenyl ether and water reaches 1kg. Stir the solution evenly, heat the container in a water bath at 100°C, and use a stirrer to stir the mixed solution in the container. Set the speed at 300 rpm, stir for 20 minutes, stop stirring when the adhesive is completely gelatinized, seal the container with a film, and continue to cook the slurry in a water bath at 95-100°C for 40 minutes. Prepare an improved sizing adhesive, wind the prepared cotton roving on a special sizing frame, immerse the sizing frame in the adhesive for sizing, take it out after 5 minutes, and place it at 80°C Dry in the oven for 30 minutes.
实施例3Example 3
用电子天枰准确称量40g磷酸酯淀粉和40g丙烯酸酯固体浆料置于1L容器底部,同时称取5g的聚氨酯和10g的乙二醇苯醚溶液加入容器,往容器中加水,使磷酸酯淀粉,丙烯酸酯,聚氨酯,乙二醇苯醚和水的总重量达到1kg,将溶液搅拌均匀,将容器置于100℃水浴锅中加热,同时使用搅拌器对容器中的混合液进行搅拌,搅拌速度设定为300转/分钟,搅拌20分钟,当粘合剂完全糊化之后,停止搅拌,用薄膜将容器密封,继续在95-100℃的水浴锅中煮浆40分钟。制备成改善后的浆纱用粘合剂,之后将准备好的棉粗纱绕在特制的浆纱架上,将浆纱架浸没的粘合剂中进行上浆,5分钟后取出,置于80℃烘箱中烘干30分钟。Use an electronic balance to accurately weigh 40g of phosphate starch and 40g of acrylate solid slurry and place them at the bottom of a 1L container. At the same time, weigh 5g of polyurethane and 10g of ethylene glycol phenyl ether solution into the container, add water to the container, and make the phosphate The total weight of starch, acrylate, polyurethane, ethylene glycol phenyl ether and water reaches 1kg. Stir the solution evenly, heat the container in a water bath at 100°C, and use a stirrer to stir the mixed solution in the container. Set the speed at 300 rpm, stir for 20 minutes, stop stirring when the adhesive is completely gelatinized, seal the container with a film, and continue to cook the slurry in a water bath at 95-100°C for 40 minutes. Prepare an improved sizing adhesive, wind the prepared cotton roving on a special sizing frame, immerse the sizing frame in the adhesive for sizing, take it out after 5 minutes, and place it at 80°C Dry in the oven for 30 minutes.
为对比本技术方案的技术优点,用电子天枰准确称量40g磷酸酯淀粉和40g丙烯酸酯固体浆料置于1L容器底部,往容器中加水,使磷酸酯淀粉,丙烯酸酯和水的总重量达到1kg,将溶液搅拌均匀,将容器置于100℃水浴锅中加热,同时使用搅拌器对容器中的混合液进行搅拌,搅拌速度设定为300转/分钟,搅拌20分钟,当粘合剂完全糊化之后,停止搅拌,用薄膜将容器密封,继续在95-100℃的水浴锅中煮浆40分钟。之后将准备好的棉粗纱绕在特制的浆纱架上,将浆纱架浸没的粘合剂中进行上浆,5分钟后取出,置于80℃烘箱中烘干30分钟。所制得的样品作为原样。将实施例1、实施例2、实施例3和原样的粗纱样品置于恒温恒湿环境下24小时,温度为20℃,湿度为65%。然后对样品进行拉伸断裂测试,样品夹持距离为5cm,拉伸速度为50mm/min。得到数据如表1:For comparing the technical advantages of this technical solution, accurately weigh 40g phosphate starch and 40g acrylate solid slurry with an electronic balance and place it at the bottom of a 1L container, add water to the container to make the total weight of phosphate starch, acrylate and water reach 1kg, stir the solution evenly, heat the container in a water bath at 100°C, and at the same time use a stirrer to stir the mixed solution in the container, set the stirring speed to 300 rpm, stir for 20 minutes, when the adhesive After complete gelatinization, stop stirring, seal the container with a film, and continue to boil the slurry for 40 minutes in a water bath at 95-100°C. Afterwards, the prepared cotton roving is wound on a special sizing frame, and the sizing frame is immersed in the binder for sizing, taken out after 5 minutes, and placed in an oven at 80°C for 30 minutes to dry. The prepared samples were taken as they were. Example 1, Example 2, Example 3 and the original roving samples were placed in a constant temperature and humidity environment for 24 hours at a temperature of 20° C. and a humidity of 65%. Then the sample was subjected to a tensile fracture test, the clamping distance of the sample was 5 cm, and the tensile speed was 50 mm/min. The data obtained are shown in Table 1:
表1 上浆粗纱样品的粘附力值和伸长率Table 1 Adhesion values and elongation of sized roving samples
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乙二醇苯醚市场分析;王忠宝 等;《精细与专用化学品》;20050121;第13卷(第2期);第23-25页 * |
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