CN103044558B - A kind of High-film-forming-prhigh-performance high-performance cationic graft starch - Google Patents
A kind of High-film-forming-prhigh-performance high-performance cationic graft starch Download PDFInfo
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- 229920002472 Starch Polymers 0.000 title claims abstract description 26
- 235000019698 starch Nutrition 0.000 title claims abstract description 26
- 239000008107 starch Substances 0.000 title claims abstract description 25
- 125000002091 cationic group Chemical group 0.000 title claims abstract description 22
- 238000006243 chemical reaction Methods 0.000 claims abstract description 34
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 claims abstract description 20
- 229920002261 Corn starch Polymers 0.000 claims abstract description 19
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims abstract description 19
- 239000008120 corn starch Substances 0.000 claims abstract description 19
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims abstract description 19
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims abstract description 19
- 229940069328 povidone Drugs 0.000 claims abstract description 19
- LTVDFSLWFKLJDQ-UHFFFAOYSA-N α-tocopherolquinone Chemical compound CC(C)CCCC(C)CCCC(C)CCCC(C)(O)CCC1=C(C)C(=O)C(C)=C(C)C1=O LTVDFSLWFKLJDQ-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000002994 raw material Substances 0.000 claims abstract description 14
- 238000006266 etherification reaction Methods 0.000 claims abstract description 13
- 238000004513 sizing Methods 0.000 claims description 19
- 229940099112 cornstarch Drugs 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 238000002156 mixing Methods 0.000 claims description 10
- 239000004744 fabric Substances 0.000 claims description 7
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 claims description 6
- 239000000839 emulsion Substances 0.000 claims description 6
- 238000004321 preservation Methods 0.000 claims description 5
- 238000007580 dry-mixing Methods 0.000 claims description 4
- 230000035484 reaction time Effects 0.000 claims description 4
- -1 3-chloro-2-hydroxypropyl Chemical group 0.000 claims description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 3
- 229910001870 ammonium persulfate Inorganic materials 0.000 claims description 3
- 239000011575 calcium Substances 0.000 claims description 3
- 229910052791 calcium Inorganic materials 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims 1
- 238000001035 drying Methods 0.000 claims 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 claims 1
- 229920000742 Cotton Polymers 0.000 abstract description 21
- 239000002002 slurry Substances 0.000 abstract description 17
- 238000004519 manufacturing process Methods 0.000 abstract description 6
- 238000009990 desizing Methods 0.000 abstract description 4
- 229920000728 polyester Polymers 0.000 abstract description 4
- 239000002351 wastewater Substances 0.000 abstract description 3
- 238000003912 environmental pollution Methods 0.000 abstract description 2
- 230000003712 anti-aging effect Effects 0.000 abstract 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 21
- 229920002451 polyvinyl alcohol Polymers 0.000 description 21
- 238000005299 abrasion Methods 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 238000007254 oxidation reaction Methods 0.000 description 5
- 238000006065 biodegradation reaction Methods 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- 239000004753 textile Substances 0.000 description 4
- 238000013329 compounding Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- HDMGAZBPFLDBCX-UHFFFAOYSA-M potassium;sulfooxy sulfate Chemical compound [K+].OS(=O)(=O)OOS([O-])(=O)=O HDMGAZBPFLDBCX-UHFFFAOYSA-M 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 230000002929 anti-fatigue Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000003094 microcapsule Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
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Abstract
本发明公开了一种高成膜性阳离子接枝高性能淀粉,该浆料由原料玉米淀粉、3-氯-2-羟丙基三甲基氯化铵、聚维酮与过硫酸盐通过干法混合醚化接枝反应而成,其中各原料的质量含量为玉米淀粉80~95%,3-氯-2-羟丙基三甲基氯化铵1~10%,聚维酮1~6%,过硫酸盐0.1~12%。本高成膜性阳离子接枝高性能淀粉对环境友好,具有良好的抗老化性能,浆液粘度稳定,对棉及涤纶均有较强粘附力抗疲劳,浆液成膜性好,易退浆,浆液废水易于处理,易生物降解,对环境污染小,在生产过程中是零污染排放。The invention discloses a cationic grafted high-performance starch with high film-forming property. It is formed by mixed etherification grafting reaction, wherein the mass content of each raw material is 80-95% of corn starch, 1-10% of 3-chloro-2-hydroxypropyltrimethylammonium chloride, 1-6% of povidone %, persulfate 0.1~12%. The high-film-forming cationic grafted high-performance starch is environmentally friendly, has good anti-aging properties, stable slurry viscosity, strong adhesion to cotton and polyester, and fatigue resistance. The slurry has good film-forming properties and is easy to desizing. Slurry wastewater is easy to handle, easy to biodegrade, has little environmental pollution, and has zero pollution discharge in the production process.
Description
技术领域technical field
本发明属于纺织工业领域,具体涉及纺织工业纱线上浆工艺中的一种高成膜性阳离子接枝高性能淀粉。The invention belongs to the field of textile industry, and in particular relates to a high-film-forming cationic grafted high-performance starch in the yarn sizing process of the textile industry.
背景技术Background technique
在纺织工业中的纱线上浆工艺中,由于聚乙烯醇(PVA)浆料具有优良的成膜性、粘附性及与其他浆料有较好相溶性的特点,被认为是解决涤棉混纺纱及纯棉细号、高密、高难品种最理想的浆料。但是,由于聚乙烯醇(PVA)浆料的价格远远高于淀粉类浆料,加之聚乙烯醇(PVA)浆料和一些难降解的浆料,退浆后的浆液废水难以处理,造成环境污染。对环境的破坏、污染问题已经引起广泛重视,尤其是经聚乙烯醇(PVA)浆料上浆的织物在出口产品中已经受限,因此,经纱上浆少用或不用聚乙烯醇(PVA)浆料,已成为亟待解决的问题。现有技术中也公开了一些非聚乙烯醇类阳离子浆料,但在高品质和特殊应用领域,现有的浆料在高成膜性、抗疲劳、高成膜性方面仍然存在不足,这严重制约了非聚乙烯醇浆料的应用范围。In the yarn sizing process in the textile industry, because polyvinyl alcohol (PVA) size has excellent film-forming properties, adhesion and better compatibility with other sizes, it is considered to solve the problem of polyester-cotton blending. The most ideal size for spinning and pure cotton fine size, high density and high difficulty varieties. However, since the price of polyvinyl alcohol (PVA) sizing is much higher than that of starch sizing, coupled with polyvinyl alcohol (PVA) sizing and some refractory sizing, it is difficult to treat the sizing wastewater after desizing, causing environmental pollution. pollute. The damage to the environment and pollution problems have attracted widespread attention, especially the fabrics sized with polyvinyl alcohol (PVA) sizing have been limited in export products, so less or no polyvinyl alcohol (PVA) sizing is used for warp sizing , has become an urgent problem to be solved. Some non-polyvinyl alcohol cationic pastes are also disclosed in the prior art, but in the field of high quality and special applications, the existing pastes still have deficiencies in high film-forming properties, fatigue resistance, and high film-forming properties. Seriously restrict the scope of application of non-polyvinyl alcohol slurry.
发明内容Contents of the invention
本发明的目的是在现有技术的基础上,提供一种低成本、性能优异且少用或不使用PVA的高成膜性阳离子接枝高性能淀粉。The purpose of the present invention is to provide a low-cost, high-performance cationic grafted high-performance starch with low or no use of PVA on the basis of the prior art.
本发明的另一目的是提供一种上述高成膜性阳离子接枝高性能淀粉的制备方法和使用方法。Another object of the present invention is to provide a method for preparing and using the above-mentioned high-film-forming cationic grafted high-performance starch.
本发明的目的可以通过以下措施达到:The purpose of the present invention can be achieved through the following measures:
一种高成膜性阳离子接枝高性能淀粉,该浆料由原料玉米淀粉、3-氯-2-羟丙基三甲基氯化铵、聚维酮与过硫酸盐通过干法混合醚化接枝反应而成,其中各原料的质量含量为玉米淀粉80~95%,3-氯-2-羟丙基三甲基氯化铵1~10%,聚维酮1~6%,过硫酸盐0.1~12%。(其中各原料之和为100%)A high-film-forming cationic grafted high-performance starch, the slurry is etherified by dry mixing raw corn starch, 3-chloro-2-hydroxypropyltrimethylammonium chloride, povidone and persulfate It is formed by grafting reaction, and the mass content of each raw material is 80-95% of corn starch, 1-10% of 3-chloro-2-hydroxypropyltrimethylammonium chloride, 1-6% of povidone, persulfuric acid Salt 0.1~12%. (the sum of each raw material is 100%)
在一种优选方案中,各原料的质量含量为:玉米淀粉80~90%,3-氯-2-羟丙基三甲基氯化铵2~8%,聚维酮1~6%,过硫酸盐1~8%。(其中各原料之和为100%)In a preferred scheme, the mass content of each raw material is: 80-90% of cornstarch, 2-8% of 3-chloro-2-hydroxypropyltrimethylammonium chloride, 1-6% of povidone, and Sulfate 1-8%. (the sum of each raw material is 100%)
在各原料的干法混合醚化接枝反应中,温度优选为60℃~75℃,进一步优选65~70℃,最优选在68℃左右。干法混合醚化接枝反应时间可根据实际情况进行调节,一般可以为30min~60min。In the dry mixing etherification grafting reaction of each raw material, the temperature is preferably 60°C-75°C, more preferably 65-70°C, and most preferably around 68°C. The reaction time of dry mixed etherification grafting can be adjusted according to the actual situation, generally it can be 30min~60min.
本发明中的过硫酸盐选自过硫酸钙、过硫酸氢钾、过硫酸铵中的一种或几种。The persulfate in the present invention is selected from one or more of calcium persulfate, potassium hydrogen persulfate and ammonium persulfate.
本发明的浆料,通过初步的混合反应将3-氯-2-羟丙基三甲基氯化铵、聚维酮与过硫酸盐采用微胶囊包埋方法进行包埋,这种先对各组分进行包埋,待使用前再进行充分反应的方式,对浆料的生产、流通、储存和使用环节都极为有利。In the slurry of the present invention, 3-chloro-2-hydroxypropyltrimethylammonium chloride, povidone and persulfate are embedded by a microcapsule embedding method through a preliminary mixing reaction. The method of embedding components and fully reacting before use is extremely beneficial to the production, circulation, storage and use of slurry.
本发明公开了一种上述高成膜性阳离子接枝高性能淀粉的使用方法:高成膜性阳离子接枝高性能淀粉在使用前,先加入水并升温至95℃~130℃进行保温反应,反应后得到对织物上浆的乳状液;The invention discloses a method for using the high-film-forming cation-grafted high-performance starch: before using the high-film-forming cation-grafted high-performance starch, add water and raise the temperature to 95°C to 130°C for heat preservation reaction. After the reaction, an emulsion for fabric sizing is obtained;
其中3-氯-2-羟丙基三甲基氯化铵、聚维酮与过硫酸盐相配合与玉米淀粉发生保温化学反应,其包括醚化、接枝、氧化复合反应等,如3-氯-2-羟丙基三甲基氯化铵与玉米淀粉在温度和聚维酮与过硫酸盐的促进下发生醚化接枝反应,过硫酸盐与玉米淀粉发生氧化反应等。Among them, 3-chloro-2-hydroxypropyltrimethylammonium chloride, povidone and persulfate cooperate with corn starch to undergo thermal insulation chemical reactions, which include etherification, grafting, oxidation compound reactions, etc., such as 3- Chloro-2-hydroxypropyltrimethylammonium chloride and corn starch undergo etherification grafting reaction under the promotion of temperature and povidone and persulfate, and persulfate and corn starch undergo oxidation reaction.
使用前的保温反应中根据生产所适用的固含量确定高成膜性阳离子接枝高性能淀粉与水的比例,高成膜性阳离子接枝高性能淀粉与水的质量比一般为10~20:80~90,优选为8~16:84~92,进一步优选为9~14:86~91。保温反应一般在搅拌下进行,保温反应的时间优选为20~50min,进一步优选为25~45min。In the insulation reaction before use, the ratio of high film-forming cationic grafted high-performance starch to water is determined according to the solid content applicable to production. The mass ratio of high film-forming cationic grafted high-performance starch to water is generally 10-20: 80-90, preferably 8-16: 84-92, more preferably 9-14: 86-91. The heat preservation reaction is generally carried out under stirring, and the time of the heat preservation reaction is preferably 20-50 minutes, more preferably 25-45 minutes.
本发明还包括一种高成膜性阳离子接枝高性能淀粉的制备方法,将原料玉米淀粉、3-氯-2-羟丙基三甲基氯化铵、聚维酮与过硫酸盐通过干法混合醚化接枝反应而得,其中各原料的质量含量为玉米淀粉80~95%,3-氯-2-羟丙基三甲基氯化铵1~10%,聚维酮1~6%,过硫酸盐0.1~12%。其中各一般或优选条件如上所述。The present invention also includes a preparation method of high-film-forming cationic grafted high-performance starch, wherein raw material cornstarch, 3-chloro-2-hydroxypropyltrimethylammonium chloride, povidone and persulfate are dried It is obtained by mixed etherification grafting reaction, wherein the mass content of each raw material is 80-95% of corn starch, 1-10% of 3-chloro-2-hydroxypropyltrimethylammonium chloride, 1-6% of povidone %, persulfate 0.1~12%. Wherein each general or preferred condition is as above.
本发明的高成膜性阳离子接枝高性能淀粉具有粘附力强、成膜性好、浆膜强韧、有良好的弹性、耐磨等性能。在纺织纯棉纱线上上浆时,一般紧度的品种80支纱以下可不用聚乙烯醇(PVA),在绦棉或80支纱以上纯棉纱线上上浆也可不用或少用聚乙烯醇(PVA)。其进一步具有如下性能:The cationic grafted high-performance starch with high film-forming property of the invention has strong adhesion, good film-forming property, strong and tough serous film, good elasticity, wear resistance and the like. When sizing pure cotton yarns for textiles, polyvinyl alcohol (PVA) may not be used for general tightness varieties below 80 counts, and polyethylene may not be used or used less for sizing cotton or pure cotton yarns above 80 counts. Alcohol (PVA). It further has the following properties:
本高成膜性阳离子接枝高性能淀粉对环境友好,不含聚乙烯醇(PVA)等能与生物降解的物质,其具有良好的高成膜性性能,浆液粘度稳定,对棉及涤纶均有较强粘附力(经浆料粘附力检测,纯棉粘附力在101.26N以上,涤棉粘附力在145.10N以上),抗疲劳,浆液成膜性好,易退浆,浆液废水易于处理,易生物降解(采用标准进行生物降解测试,下同,结果达9级),对环境污染小,在生产过程中是零污染排放。The high-film-forming cationic grafted high-performance starch is environmentally friendly and does not contain polyvinyl alcohol (PVA) and other biodegradable substances. It has good high film-forming performance, stable slurry viscosity, and is suitable for cotton and polyester. It has strong adhesion (tested by slurry adhesion, the adhesion of pure cotton is above 101.26N, and the adhesion of polyester and cotton is above 145.10N), anti-fatigue, good slurry film-forming property, easy to desizing, slurry Wastewater is easy to treat and biodegradable (using The biodegradation test is carried out according to the standard, the same below, and the result reaches level 9), which has little pollution to the environment and has zero pollution discharge during the production process.
具体实施方式Detailed ways
实施例1Example 1
将玉米淀粉83kg,3-氯-2-羟丙基三甲基氯化铵6kg,、聚维酮6㎏,过硫酸钙5kg,分别装入反应罐,在68℃温度下进行干法混合醚化接枝反应45min后终止反应,卸料包装、入库。客户在使用时,再加800kg清水糊化升温至95℃或在高压罐中加清水升温至125℃保温30~45min进行醚化、氧化复合反应而制得对织物上浆的乳状液。Put 83kg of corn starch, 6kg of 3-chloro-2-hydroxypropyltrimethylammonium chloride, 6kg of povidone, and 5kg of calcium persulfate into the reaction tank respectively, and dry-mix ether at 68°C The chemical grafting reaction was terminated after 45 minutes, and the material was unloaded, packaged, and put into storage. When the customer is using it, add 800kg of clear water to gelatinize and heat up to 95°C or add clear water in a high-pressure tank to heat up to 125°C and keep it warm for 30-45min to carry out etherification and oxidation compound reactions to prepare the emulsion for fabric sizing.
经浆料粘附力检测,其纯棉粘附力为112N,涤棉粘附力为156N。分别对CN102733190A、CN102733191A、CN102605618A中的实施例1制备的浆料进行相同的粘附力检测,其中CN102733190A纯棉粘附力为91N,涤棉粘附力为115N;CN102733191A纯棉粘附力为93N,涤棉粘附力为119N;CN102605618A纯棉粘附力为66N,涤棉粘附力为97N。其生物降解测试9级。After the slurry adhesion test, the pure cotton adhesion is 112N, and the polyester-cotton adhesion is 156N. Carry out the same adhesion test to the slurry prepared in Example 1 in CN102733190A, CN102733191A, and CN102605618A respectively, wherein CN102733190A pure cotton adhesion is 91N, polyester cotton adhesion is 115N; CN102733191A pure cotton adhesion is 93N , polyester-cotton adhesion is 119N; CN102605618A pure cotton adhesion is 66N, polyester-cotton adhesion is 97N. Its biodegradation test grade 9.
对本品与试验一辅料复配得到的浆膜进行强韧、耐磨测试,其磨耗:本产品是1.22mg/cm2,聚乙烯醇(PVA)是1.18mg/cm2;本品浆膜断裂伸长率:3.69%。分别以CN102733190A、CN102733191A、CN102605618A中的实施例1制备的浆料进行同条件下对比实验,CN102733190A磨耗1.65mg/cm2,CN102733191A磨耗1.92mg/cm2,CN102605618A磨耗1.84mg/cm2。The toughness and wear resistance tests were carried out on the serous film obtained by compounding this product with the auxiliary materials in test 1. The abrasion resistance of this product was 1.22 mg/cm 2 , and that of polyvinyl alcohol (PVA) was 1.18 mg/cm 2 ; the serous film of this product Elongation at break: 3.69%. The slurries prepared in Example 1 in CN102733190A, CN102733191A, and CN102605618A were respectively used for comparative experiments under the same conditions. CN102733190A had an abrasion of 1.65 mg/cm 2 , CN102733191A had an abrasion of 1.92 mg/cm 2 , and CN102605618A had an abrasion of 1.84 mg/cm 2 .
实施例2Example 2
将玉米淀粉85kg,3-氯-2-羟丙基三甲基氯化铵6kg,、聚维酮4㎏,过硫酸氢钾5kg,分别装入反应罐,在68℃温度下进行干法混合醚化接枝反应45min后终止反应,卸料包装、入库。客户在使用时,再加700kg清水糊化升温至95℃或在高压罐中加清水升温至125℃保温30~45min进行醚化、氧化复合反应而制得织物上浆的乳状液。经浆料粘附力检测,其纯棉粘附力为104N,涤棉粘附力为147N。其生物降解测试9级。对本品与试验一辅料复配得到的浆膜进行强韧、耐磨测试,其磨耗:本产品是1.26mg/cm2。Put 85kg of cornstarch, 6kg of 3-chloro-2-hydroxypropyltrimethylammonium chloride, 4kg of povidone, and 5kg of potassium hydrogen persulfate into the reaction tank respectively, and dry mix them at a temperature of 68°C After 45 minutes of etherification and grafting reaction, the reaction was terminated, and the materials were unloaded, packaged, and put into storage. When the customer is using it, add 700kg of water to gelatinize and heat up to 95°C or add water in a high-pressure tank to heat up to 125°C and keep it warm for 30-45min to carry out etherification and oxidation compound reactions to obtain a fabric sizing emulsion. After the slurry adhesion test, the pure cotton adhesion is 104N, and the polyester-cotton adhesion is 147N. Its biodegradation test grade 9. The toughness and abrasion resistance tests were carried out on the serous film obtained by compounding this product with the auxiliary material of test 1. The abrasion resistance of this product was 1.26mg/cm 2 .
实施例3Example 3
将玉米淀粉90kg,3-氯-2-羟丙基三甲基氯化铵4kg,、聚维酮3㎏,过硫酸铵3kg,分别装入反应罐,在68℃温度下进行复合混合反应45min后终止反应,卸料包装、入库。客户在使用时,再加680kg清水糊化升温至95℃或在高压罐中加清水升温至125℃保温30~45min进行醚化、氧化复合反应而制得织物上浆的乳状液。经浆料粘附力检测,其纯棉粘附力为108N,涤棉粘附力为155N。其生物降解测试9级。对本品与试验一辅料复配得到的浆膜进行强韧、耐磨测试,其磨耗:本产品是1.30mg/cm2。Put 90kg of cornstarch, 4kg of 3-chloro-2-hydroxypropyltrimethylammonium chloride, 3kg of povidone, and 3kg of ammonium persulfate into the reaction tank respectively, and carry out compound mixing reaction at 68°C for 45min Finally, the reaction is terminated, unloaded, packaged, and put into storage. When the customer is using it, add 680kg of water to gelatinize and heat up to 95°C or add water in a high-pressure tank to heat up to 125°C and keep it warm for 30-45min to carry out etherification and oxidation compound reactions to obtain fabric sizing emulsion. After the slurry adhesion test, the pure cotton adhesion is 108N, and the polyester-cotton adhesion is 155N. Its biodegradation test grade 9. The toughness and abrasion resistance tests were carried out on the serous film obtained by compounding this product with the auxiliary material of test 1. The abrasion resistance of this product was 1.30 mg/cm 2 .
采用上述各实施例所得乳状液浆料全部或部分替代现有浆料配方中的聚乙烯醇、高性能淀粉和普通淀粉,在实际生产中对织物进行上浆处理,并采用现有配方做对照实验。各组配方及生产条件见下表。All or part of the emulsion size obtained in the above examples is used to replace the polyvinyl alcohol, high-performance starch and ordinary starch in the existing size formula, and the fabric is sized in actual production, and the existing formula is used for comparative experiments . The formulations and production conditions of each group are shown in the table below.
试验一test one
品种:65"JC100S×JC100S/2/216×125规格尺寸Variety: 65"JC100 S × JC100 S /2/216 × 125 size
上浆工艺Sizing process
1、选用机型:1. Selected models:
丰田双浆槽七单元,采用“单浸双压”工艺Seven units of Toyota double pulp tank, adopting "single immersion double pressure" process
2、浆纱工艺:2. Sizing process:
车速:50M/minSpeed: 50M/min
浆槽温度:95℃Slurry tank temperature: 95°C
浆槽粘度:前/后8.7/8.5S Viscosity of stock tank: front/back 8.7/8.5 S
锡林温度:预/并108/93℃Cylinder temperature: pre/combined 108/93°C
压浆力:Ⅰ速16KNⅡ速24KNGrouting force: Ⅰ speed 16KN Ⅱ speed 24KN
退绕张力:0.06mpaUnwinding tension: 0.06mpa
浆槽张力:Ⅰ速0.3%Ⅱ速0.2%Tension of stock tank: Ⅰ speed 0.3% Ⅱ speed 0.2%
湿区牵引力:Ⅰ速0.4%Ⅱ速0.3%Wet area traction: I speed 0.4% II speed 0.3%
干区张力:Ⅰ速0.2%Ⅱ速0.1%Tension in dry area: 0.2% for Ⅰ speed and 0.1% for Ⅱ speed
卷取张力:1700NCoiling tension: 1700N
回潮显示:7.5%Resurgence display: 7.5%
退浆率:13.7%Desizing rate: 13.7%
3、织造情况3. Weaving condition
试验二:Test two:
品种:63"T/C65/3545S×45S/133×721/1规格尺寸Variety: 63"T/C65/3545 S × 45 S /133 × 721/1 size
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CN101875701A (en) * | 2010-02-03 | 2010-11-03 | 内蒙古奈伦农业科技股份有限公司 | Preparation method of oxidative cationic modified starch slurry |
CN102605618A (en) * | 2012-03-14 | 2012-07-25 | 宜兴市军达浆料科技有限公司 | Multi-component high-performance sizing agent |
CN102733190A (en) * | 2012-07-12 | 2012-10-17 | 宜兴市军达浆料科技有限公司 | Cation high performance slurry |
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US4373099A (en) * | 1981-10-07 | 1983-02-08 | Grain Processing Corporation | Continuous process for preparation of a thinned cationic starch paste |
CN101724083A (en) * | 2010-01-15 | 2010-06-09 | 广西大学 | Method for producing modified starch |
CN101875701A (en) * | 2010-02-03 | 2010-11-03 | 内蒙古奈伦农业科技股份有限公司 | Preparation method of oxidative cationic modified starch slurry |
CN102605618A (en) * | 2012-03-14 | 2012-07-25 | 宜兴市军达浆料科技有限公司 | Multi-component high-performance sizing agent |
CN102733190A (en) * | 2012-07-12 | 2012-10-17 | 宜兴市军达浆料科技有限公司 | Cation high performance slurry |
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