CN108677533A - 一种提高棉线硬度的方法 - Google Patents
一种提高棉线硬度的方法 Download PDFInfo
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- CN108677533A CN108677533A CN201810402933.1A CN201810402933A CN108677533A CN 108677533 A CN108677533 A CN 108677533A CN 201810402933 A CN201810402933 A CN 201810402933A CN 108677533 A CN108677533 A CN 108677533A
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- 229920000742 Cotton Polymers 0.000 title claims abstract description 57
- 238000000034 method Methods 0.000 title claims abstract description 14
- 239000000463 material Substances 0.000 claims abstract description 65
- 239000007788 liquid Substances 0.000 claims abstract description 11
- 238000002156 mixing Methods 0.000 claims abstract description 11
- 238000011017 operating method Methods 0.000 claims abstract description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 22
- 238000007654 immersion Methods 0.000 claims description 20
- 239000000843 powder Substances 0.000 claims description 18
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical class O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims description 17
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims description 15
- 239000000203 mixture Substances 0.000 claims description 15
- 230000009514 concussion Effects 0.000 claims description 14
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 10
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 claims description 10
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims description 10
- 239000008367 deionised water Substances 0.000 claims description 9
- 229910021641 deionized water Inorganic materials 0.000 claims description 9
- 230000000694 effects Effects 0.000 claims description 7
- KOMNUTZXSVSERR-UHFFFAOYSA-N 1,3,5-tris(prop-2-enyl)-1,3,5-triazinane-2,4,6-trione Chemical compound C=CCN1C(=O)N(CC=C)C(=O)N(CC=C)C1=O KOMNUTZXSVSERR-UHFFFAOYSA-N 0.000 claims description 5
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 5
- QWGRWMMWNDWRQN-UHFFFAOYSA-N 2-methylpropane-1,3-diol Chemical compound OCC(C)CO QWGRWMMWNDWRQN-UHFFFAOYSA-N 0.000 claims description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 5
- 239000004925 Acrylic resin Substances 0.000 claims description 5
- 229920000178 Acrylic resin Polymers 0.000 claims description 5
- 239000002202 Polyethylene glycol Substances 0.000 claims description 5
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- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 5
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 claims description 5
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- 235000010299 hexamethylene tetramine Nutrition 0.000 claims description 5
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- 229940100573 methylpropanediol Drugs 0.000 claims description 5
- SOQBVABWOPYFQZ-UHFFFAOYSA-N oxygen(2-);titanium(4+) Chemical compound [O-2].[O-2].[Ti+4] SOQBVABWOPYFQZ-UHFFFAOYSA-N 0.000 claims description 5
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- 229920001568 phenolic resin Polymers 0.000 claims description 5
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- 229920005989 resin Polymers 0.000 claims description 5
- 238000012216 screening Methods 0.000 claims description 5
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- -1 sugar alcohol ester Chemical class 0.000 claims description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
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- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims 1
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- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims 1
- GTDHYNXLIKNVTJ-UHFFFAOYSA-N n-(1-hydroxy-2-methylpropan-2-yl)octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NC(C)(C)CO GTDHYNXLIKNVTJ-UHFFFAOYSA-N 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
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- 229910021536 Zeolite Inorganic materials 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 8
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- 150000002191 fatty alcohols Chemical class 0.000 description 8
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- 241000471262 Ardisia japonica Species 0.000 description 4
- 241001643874 Cymbopogon distans Species 0.000 description 4
- 241000490229 Eucephalus Species 0.000 description 4
- 235000011201 Ginkgo Nutrition 0.000 description 4
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- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 4
- 235000003143 Panax notoginseng Nutrition 0.000 description 4
- 241000180649 Panax notoginseng Species 0.000 description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
- 241000220259 Raphanus Species 0.000 description 4
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- 150000008065 acid anhydrides Chemical class 0.000 description 4
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 description 4
- 238000000227 grinding Methods 0.000 description 4
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 4
- 239000011976 maleic acid Substances 0.000 description 4
- 238000003801 milling Methods 0.000 description 4
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- RKISUIUJZGSLEV-UHFFFAOYSA-N n-[2-(octadecanoylamino)ethyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCNC(=O)CCCCCCCCCCCCCCCCC RKISUIUJZGSLEV-UHFFFAOYSA-N 0.000 description 4
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- 238000010792 warming Methods 0.000 description 4
- 239000012267 brine Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 2
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- 230000009286 beneficial effect Effects 0.000 description 1
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- 231100000252 nontoxic Toxicity 0.000 description 1
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- 231100000765 toxin Toxicity 0.000 description 1
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Abstract
一种提高棉线硬度的方法,涉及纺织加工技术领域,其特征在于:包括以下操作步骤,选取材料、初次浸泡、混合材料、进行除杂、再次浸泡、进行除液。本发明方法合理、实施方便、产品强度高、拉伸性能良好。
Description
技术领域
本发明涉及纺织加工技术领域,具体涉及一种提高棉线硬度的方法。
背景技术
棉线是用棉花纤维搓纺而成的线。
现在的棉线我发现有好多,有各种各样的名字,但是不外乎全棉的,晴 棉的(也就是混纺的)全晴的和人造棉的。棉线是用棉花纤维搓纺而成的线。 装订用棉线有上光与不上光两种,包装形式有直轴型、塔轴型两种。塔轴型 多用于锁线加工,其规格根据专业标准有以下几种:42支纱4股和6股,60支纱 4股和6股的白色蜡光塔线,其型号分别为S424,S426、S604、S606,也可记 作42S/4、42S/6、60S/4、60S/6,其中S表示支纱,斜线下的数字表示股数装 订用棉线有上光与不上光两种,包装形式有直轴型、塔轴型两种。塔轴型多 用于锁线加工,其规格根据专业标准有以下几种:42支纱4股和6股,60支纱4 股和6股的白色蜡光塔线,其型号分别为S424,S426、S604、S606,也可记作 42S/4、42S/6、60S/4、60S/6,其中S表示支纱,斜线下的数字表示股数。
常温下,在一杯清水中不断加入食盐,并用筷子不停地搅拌,直到食盐 不再溶解为止。将一根棉线放入配制好的浓盐水里浸泡一下,拿出来放在桌 上晾干。将晾干后的用手提起,点燃一根火柴去烧棉线。这时,你会发现, 棉线从下端一直燃烧到上端,但烧过后的线灰仍象一根线一样没有被烧断。 为了方便比较,我们再来烧一根没有浸过盐水的普通棉线,结果,烧完的棉 线没有留存下线灰。
但是现在的许多的棉线的硬度都不是特别的好,一拉就断,而且棉线断 了之后会有多余的线头,这样在后续的使用上要重新清理,也非常的不方便, 而且由于硬度不高,往往在某些特定的加工时候会浪费更加的多的时间。
发明内容
本发明所要解决的技术问题在于克服现有的技术缺陷提供一种方法合 理、实施方便、产品强度高、拉伸性能良好的一种提高棉线硬度的方法。
本发明所要解决的技术问题采用以下的技术方案来实现:
一种提高棉线硬度的方法,其特征在于:包括以下操作步骤,
步骤一、选取材料:选取已经制备好的棉线,然后放在清水中浸泡25-35 分钟,然后放在干燥、温度为50-60℃的房间中静置,直至水分消失;
步骤二、初次浸泡:将静置后的棉线取出然后放入一份浸泡液中浸泡2-3 个小时;
步骤三、混合材料:将浸泡后的棉线放入设备中,且加入混合料然后震 荡混合30-45分钟;由于材料上有液体,从而具有一定的吸附效果;
步骤四、进行除杂:将混合后的材料放置在振动筛网上进行震荡筛选, 将多余的料震荡除去;
步骤五、再次浸泡:将震荡后的材料放入另一份浸泡液中浸泡2-3个小时;
步骤六、进行除液:将浸泡后的材料放入干燥、温度为65-75℃的房间中 静置,直至水分消失;
所述浸泡液包括以下重量份的材料制成,
丙烯酸树脂19-27份、纳米二氧化钛4-9份、甲乙酮1-5份、硅烷偶联剂 KH-5508-12份、氮化铝粉1-4份、硅酸乙酯5-9份、异氰尿酸三缩水甘油酯4-10 份、甲基丙二醇5-10份、乙撑双硬脂酰胺2-7份、生物助剂6-10份;
制备方式:将上述的材料依次置于反应釜中混合均匀,升温至220-260℃, 保温搅拌1~2h,得到混合料静置备用;然后加入重量份30份的去离子水且降 温到100-120℃,混合搅拌至形成流动性好的浆体;
所述生物助剂包括以下重量份的材料制成,
三七1份、天南星2份、五倍子3份、罂粟壳4份、莱菔子5份、玉竹6份、 苏子1份、紫苑2份、银杏3份、矮地茶5份、芸香草4份、三棱6份;
制备方式为:制备方式为:将上述的材料放在85-95℃的烘干设备中平铺, 然后烘干4-5个小时,然后放入研磨设备中研磨成粉末状即可;
所述混合料包括以下重量份的材料制成,
酚醛树脂14-20份、改性沸石粉5-10份、醋丙乳液4-9份、重晶石粉7-13 份、马来酸酐1-5份、六次甲基四胺5-9份、山犁糖醇酯2-9份、三烯丙基异氰 脲酸酯4-9份、聚乙二醇二缩水甘油醚1-3份、去离子水25-30份;
制备方式:将上述的材料放入反应釜中,然后升温至170-200℃,保温搅 拌1~2h,得到混合浆料;然后将浆料压入三辊机中,研磨至粒径小于20μm, 装罐即可;
所述改性沸石粉的制备方式为:将沸石研磨且过300-400目筛,然后加入 脂肪醇聚氧乙烯醚在常温下搅拌混合10min,然后升温至80-85℃保温研磨 30min,再加水搅拌制成固含量达到25-35%的溶液,所得混合液送入喷雾干燥 机中干燥,制得20-40目的球形颗粒,并于100-110℃下烘干;
所述脂肪醇聚氧乙烯醚与沸石的质量比为1:4.1;
所述棉线为人造棉或者混纺棉中的一种。
本发明的有益效果为:本发明的产品适用于工业生产,不适用于服装、 家装产品的生产,而使用的混合料、浸泡液不是常规的产品,且也可以与其 他的原料混合使用,而且产品的耐磨、拉伸的性能都非常的好,而且非常的 紧致,保证在持续拉拽的过程中不会出现断裂,而且产品的强度、韧性都性 能非常的好,并且使用的生物助剂不仅能够起到中和毒素的效果,还能够增 加产品的韧性以及耐压、耐磨的性能,产品能够用于多种基体材质上,产品 功能广,而且物耗少、成本低、无毒无副反应,可加工性能好、成型容易。
具体实施方式
为了使本发明实现的技术手段、创作特征、达成目的与功效易于明白了 解,下面进一步阐述本发明。
实施例1
一种提高棉线硬度的方法,其特征在于:包括以下操作步骤,
步骤一、选取材料:选取已经制备好的棉线,然后放在清水中浸泡25分 钟,然后放在干燥、温度为50℃的房间中静置,直至水分消失;
步骤二、初次浸泡:将静置后的棉线取出然后放入一份浸泡液中浸泡2个 小时;
步骤三、混合材料:将浸泡后的棉线放入设备中,且加入混合料然后震 荡混合30分钟;由于材料上有液体,从而具有一定的吸附效果;
步骤四、进行除杂:将混合后的材料放置在振动筛网上进行震荡筛选, 将多余的料震荡除去;
步骤五、再次浸泡:将震荡后的材料放入另一份浸泡液中浸泡2个小时;
步骤六、进行除液:将浸泡后的材料放入干燥、温度为65℃的房间中静 置,直至水分消失;
所述浸泡液包括以下重量份的材料制成,
丙烯酸树脂19-27份、纳米二氧化钛4-9份、甲乙酮1-5份、硅烷偶联剂 KH-550 8-12份、氮化铝粉1-4份、硅酸乙酯5-9份、异氰尿酸三缩水甘油酯4-10 份、甲基丙二醇5-10份、乙撑双硬脂酰胺2-7份、生物助剂6-10份;
制备方式:将上述的材料依次置于反应釜中混合均匀,升温至220-260℃, 保温搅拌1~2h,得到混合料静置备用;然后加入重量份30份的去离子水且降 温到100-120℃,混合搅拌至形成流动性好的浆体;
所述生物助剂包括以下重量份的材料制成,
三七1份、天南星2份、五倍子3份、罂粟壳4份、莱菔子5份、玉竹6份、 苏子1份、紫苑2份、银杏3份、矮地茶5份、芸香草4份、三棱6份;
制备方式为:制备方式为:将上述的材料放在85-95℃的烘干设备中平铺, 然后烘干4-5个小时,然后放入研磨设备中研磨成粉末状即可;
所述混合料包括以下重量份的材料制成,
酚醛树脂14-20份、改性沸石粉5-10份、醋丙乳液4-9份、重晶石粉7-13 份、马来酸酐1-5份、六次甲基四胺5-9份、山犁糖醇酯2-9份、三烯丙基异氰 脲酸酯4-9份、聚乙二醇二缩水甘油醚1-3份、去离子水25-30份;
制备方式:将上述的材料放入反应釜中,然后升温至170-200℃,保温搅 拌1~2h,得到混合浆料;然后将浆料压入三辊机中,研磨至粒径小于20μm, 装罐即可;
所述改性沸石粉的制备方式为:将沸石研磨且过300-400目筛,然后加入 脂肪醇聚氧乙烯醚在常温下搅拌混合10min,然后升温至80-85℃保温研磨 30min,再加水搅拌制成固含量达到25-35%的溶液,所得混合液送入喷雾干燥 机中干燥,制得20-40目的球形颗粒,并于100-110℃下烘干;
所述脂肪醇聚氧乙烯醚与沸石的质量比为1:4.1;
所述棉线为人造棉或者混纺棉中的一种。
实施例2
一种提高棉线硬度的方法,其特征在于:包括以下操作步骤,
步骤一、选取材料:选取已经制备好的棉线,然后放在清水中浸泡25分 钟,然后放在干燥、温度为50℃的房间中静置,直至水分消失;
步骤二、初次浸泡:将静置后的棉线取出然后放入一份浸泡液中浸泡2个 小时;
步骤三、混合材料:将浸泡后的棉线放入设备中,且加入混合料然后震 荡混合30分钟;由于材料上有液体,从而具有一定的吸附效果;
步骤四、进行除杂:将混合后的材料放置在振动筛网上进行震荡筛选, 将多余的料震荡除去;
步骤五、再次浸泡:将震荡后的材料放入另一份浸泡液中浸泡2个小时;
步骤六、进行除液:将浸泡后的材料放入干燥、温度为65℃的房间中静 置,直至水分消失;
所述浸泡液包括以下重量份的材料制成,
丙烯酸树脂19-27份、纳米二氧化钛4-9份、甲乙酮1-5份、硅烷偶联剂 KH-5508-12份、氮化铝粉1-4份、硅酸乙酯5-9份、异氰尿酸三缩水甘油酯4-10 份、甲基丙二醇5-10份、乙撑双硬脂酰胺2-7份、生物助剂6-10份;
制备方式:将上述的材料依次置于反应釜中混合均匀,升温至220-260℃, 保温搅拌1~2h,得到混合料静置备用;然后加入重量份30份的去离子水且降 温到100-120℃,混合搅拌至形成流动性好的浆体;
所述生物助剂包括以下重量份的材料制成,
三七1份、天南星2份、五倍子3份、罂粟壳4份、莱菔子5份、玉竹6份、 苏子1份、紫苑2份、银杏3份、矮地茶5份、芸香草4份、三棱6份;
制备方式为:制备方式为:将上述的材料放在85-95℃的烘干设备中平铺, 然后烘干4-5个小时,然后放入研磨设备中研磨成粉末状即可;
所述混合料包括以下重量份的材料制成,
酚醛树脂14-20份、改性沸石粉5-10份、醋丙乳液4-9份、重晶石粉7-13 份、马来酸酐1-5份、六次甲基四胺5-9份、山犁糖醇酯2-9份、三烯丙基异氰 脲酸酯4-9份、聚乙二醇二缩水甘油醚1-3份、去离子水25-30份;
制备方式:将上述的材料放入反应釜中,然后升温至170-200℃,保温搅 拌1~2h,得到混合浆料;然后将浆料压入三辊机中,研磨至粒径小于20μm, 装罐即可;
所述改性沸石粉的制备方式为:将沸石研磨且过300-400目筛,然后加入 脂肪醇聚氧乙烯醚在常温下搅拌混合10min,然后升温至80-85℃保温研磨 30min,再加水搅拌制成固含量达到25-35%的溶液,所得混合液送入喷雾干燥 机中干燥,制得20-40目的球形颗粒,并于100-110℃下烘干;
所述脂肪醇聚氧乙烯醚与沸石的质量比为1:4.1;
所述棉线为人造棉或者混纺棉中的一种。
实施例3
一种提高棉线硬度的方法,其特征在于:包括以下操作步骤,
步骤一、选取材料:选取已经制备好的棉线,然后放在清水中浸泡29分 钟,然后放在干燥、温度为59℃的房间中静置,直至水分消失;
步骤二、初次浸泡:将静置后的棉线取出然后放入一份浸泡液中浸泡2.2 个小时;
步骤三、混合材料:将浸泡后的棉线放入设备中,且加入混合料然后震 荡混合39分钟;由于材料上有液体,从而具有一定的吸附效果;
步骤四、进行除杂:将混合后的材料放置在振动筛网上进行震荡筛选, 将多余的料震荡除去;
步骤五、再次浸泡:将震荡后的材料放入另一份浸泡液中浸泡2.2个小时;
步骤六、进行除液:将浸泡后的材料放入干燥、温度为69℃的房间中静 置,直至水分消失;
所述浸泡液包括以下重量份的材料制成,
丙烯酸树脂19-27份、纳米二氧化钛4-9份、甲乙酮1-5份、硅烷偶联剂 KH-550 8-12份、氮化铝粉1-4份、硅酸乙酯5-9份、异氰尿酸三缩水甘油酯4-10 份、甲基丙二醇5-10份、乙撑双硬脂酰胺2-7份、生物助剂6-10份;
制备方式:将上述的材料依次置于反应釜中混合均匀,升温至220-260℃, 保温搅拌1~2h,得到混合料静置备用;然后加入重量份30份的去离子水且降 温到100-120℃,混合搅拌至形成流动性好的浆体;
所述生物助剂包括以下重量份的材料制成,
三七1份、天南星2份、五倍子3份、罂粟壳4份、莱菔子5份、玉竹6份、 苏子1份、紫苑2份、银杏3份、矮地茶5份、芸香草4份、三棱6份;
制备方式为:制备方式为:将上述的材料放在85-95℃的烘干设备中平铺, 然后烘干4-5个小时,然后放入研磨设备中研磨成粉末状即可;
所述混合料包括以下重量份的材料制成,
酚醛树脂14-20份、改性沸石粉5-10份、醋丙乳液4-9份、重晶石粉7-13 份、马来酸酐1-5份、六次甲基四胺5-9份、山犁糖醇酯2-9份、三烯丙基异氰 脲酸酯4-9份、聚乙二醇二缩水甘油醚1-3份、去离子水25-30份;
制备方式:将上述的材料放入反应釜中,然后升温至170-200℃,保温搅 拌1~2h,得到混合浆料;然后将浆料压入三辊机中,研磨至粒径小于20μm, 装罐即可;
所述改性沸石粉的制备方式为:将沸石研磨且过300-400目筛,然后加入 脂肪醇聚氧乙烯醚在常温下搅拌混合10min,然后升温至80-85℃保温研磨 30min,再加水搅拌制成固含量达到25-35%的溶液,所得混合液送入喷雾干燥 机中干燥,制得20-40目的球形颗粒,并于100-110℃下烘干;
所述脂肪醇聚氧乙烯醚与沸石的质量比为1:4.1;
所述棉线为人造棉或者混纺棉中的一种。
通过实验,测定本发明实施例1-3与普通混纺棉的性能与效果,如下表:
以上显示和描述了本发明的基本原理和主要特征和本发明的优点。本行 业的技术人员应该了解,本发明不受上述实施例的限制,上述实施例和说明 书中描述的只是说明本发明的原理,在不脱离本发明精神和范围的前提下, 本发明还会有各种变化和改进,这些变化和改进都落入要求保护的本发明范 围内。本发明要求保护范围由所附的权利要求书及其等效物界定。
Claims (3)
1.一种提高棉线硬度的方法,其特征在于:包括以下操作步骤,
步骤一、选取材料:选取已经制备好的棉线,然后放在清水中浸泡25-35分钟,然后放在干燥、温度为50-60℃的房间中静置,直至水分消失;
步骤二、初次浸泡:将静置后的棉线取出然后放入一份浸泡液中浸泡2-3个小时;
步骤三、混合材料:将浸泡后的棉线放入设备中,且加入混合料然后震荡混合30-45分钟;由于材料上有液体,从而具有一定的吸附效果;
步骤四、进行除杂:将混合后的材料放置在振动筛网上进行震荡筛选,将多余的料震荡除去;
步骤五、再次浸泡:将震荡后的材料放入另一份浸泡液中浸泡2-3个小时;
步骤六、进行除液:将浸泡后的材料放入干燥、温度为65-75℃的房间中静置,直至水分消失。
2.根据权利要求1所述的一种提高棉线硬度的方法,其特征在于:所述浸泡液包括以下重量份的材料制成,
丙烯酸树脂19-27份、纳米二氧化钛4-9份、甲乙酮1-5份、硅烷偶联剂KH-5508-12份、氮化铝粉1-4份、硅酸乙酯5-9份、异氰尿酸三缩水甘油酯4-10份、甲基丙二醇5-10份、乙撑双硬脂酰胺2-7份、生物助剂6-10份。
3.根据权利要求1所述的一种提高棉线硬度的方法,其特征在于:所述混合料包括以下重量份的材料制成,
酚醛树脂14-20份、改性沸石粉5-10份、醋丙乳液4-9份、重晶石粉7-13份、马来酸酐1-5份、六次甲基四胺5-9份、山犁糖醇酯2-9份、三烯丙基异氰脲酸酯4-9份、聚乙二醇二缩水甘油醚1-3份、去离子水25-30份。
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