CN106113847A - 一种防断裂无纺布的制备方法 - Google Patents
一种防断裂无纺布的制备方法 Download PDFInfo
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- CN106113847A CN106113847A CN201610538368.2A CN201610538368A CN106113847A CN 106113847 A CN106113847 A CN 106113847A CN 201610538368 A CN201610538368 A CN 201610538368A CN 106113847 A CN106113847 A CN 106113847A
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- 238000002360 preparation method Methods 0.000 title claims abstract description 24
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- 229920002472 Starch Polymers 0.000 claims abstract description 28
- 239000008107 starch Substances 0.000 claims abstract description 28
- 235000019698 starch Nutrition 0.000 claims abstract description 28
- 239000000835 fiber Substances 0.000 claims abstract description 25
- 239000010409 thin film Substances 0.000 claims abstract description 21
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 9
- 238000003786 synthesis reaction Methods 0.000 claims abstract description 9
- 238000004519 manufacturing process Methods 0.000 claims abstract description 8
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- 238000007731 hot pressing Methods 0.000 claims abstract description 5
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 51
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 48
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 34
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 claims description 32
- 238000003756 stirring Methods 0.000 claims description 32
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 claims description 24
- -1 phosphoric acid hydrogen Chemical class 0.000 claims description 21
- 239000001257 hydrogen Substances 0.000 claims description 17
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- 239000000463 material Substances 0.000 claims description 17
- 229920002261 Corn starch Polymers 0.000 claims description 16
- 229910019142 PO4 Inorganic materials 0.000 claims description 16
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 16
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 16
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 16
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 claims description 16
- 238000006243 chemical reaction Methods 0.000 claims description 16
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- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 14
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 claims description 14
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- 238000000034 method Methods 0.000 claims description 4
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- 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 2
- 229910052708 sodium Inorganic materials 0.000 claims 2
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- 239000005864 Sulphur Substances 0.000 claims 1
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- 239000007789 gas Substances 0.000 claims 1
- 238000012423 maintenance Methods 0.000 claims 1
- 159000000000 sodium salts Chemical class 0.000 claims 1
- 239000002562 thickening agent Substances 0.000 claims 1
- 230000009286 beneficial effect Effects 0.000 abstract description 2
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- 239000011574 phosphorus Substances 0.000 description 6
- 238000004026 adhesive bonding Methods 0.000 description 3
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- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
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- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 2
- 229910052939 potassium sulfate Inorganic materials 0.000 description 2
- 235000011151 potassium sulphates Nutrition 0.000 description 2
- 239000012808 vapor phase Substances 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
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- VUZPPFZMUPKLLV-UHFFFAOYSA-N methane;hydrate Chemical compound C.O VUZPPFZMUPKLLV-UHFFFAOYSA-N 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
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- 239000002985 plastic film Substances 0.000 description 1
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Abstract
一种防断裂无纺布的制备方法,包括薄膜的制备、纤维层的制备,制成网状的长纤维层,将短纤维制成短纤维层;纤维硬化、胶水的制备、将长纤维层附在薄膜上方,短纤维层附在薄膜下方,中间涂上胶水,通过热压,完成合成。本发明的有益效果是:本发明所采用的淀粉来源丰富、价格低廉,对环境友好;并且制得的无纺布强度高、生产成本低、可生物降解,能有效缓解白色污染问题,存放时间长,耐高温,耐水,延长使用寿命,减少白色污染,保护环境。
Description
技术领域:
本发明涉及无纺布生产技术领域,具体涉及一种防断裂无纺布的制备方法。
背景技术:
随着塑料工业的蓬勃发展,废旧塑料薄膜垃圾带来的环境污染也日趋严重,白色污染成为全球瞩目的环境问题。因此,人们必须要加大力度去开发生物可降解的塑料薄膜,治理塑料废弃物对环境所带来污染问题。
无纺布占据了薄膜一部分市场,强度较薄膜强,但是寿命短,阳光直射,长时间无纺布即变脆。
淀粉是一种来源丰富、价格低廉的天然高分子材料,也是一种取之不尽用之不竭的可再生资源,它能在多种环境条件下被生物降解,最终降解产物二氧化碳和水可以通过植物的光合作用再循环,不会对环境造成任何污染。然而淀粉分子链上含有大量羟基,容易在分子链内和分子链外形成氢键,因此难溶、难熔,并且耐水性差,一遇水或长期存放在潮湿空气中容易吸收水分,影响其稳定性。
发明内容:
本发明所要解决的技术问题在于提供一种工艺简单、生产成本低且对环境友好的防断裂无纺布的制备方法。
本发明所要解决的技术问题采用以下的技术方案来实现:
一种防断裂无纺布的制备方法,包括:
1)薄膜的制备:磷酸氢二钠15-20份、玉米淀粉100-150份、苯酚15-20份、十二烷基苯磺酸钠盐2-5份、OP-101-3份、过硫酸钾1-2份醋酸乙烯160-180份、邻苯二甲酸二丁酯1-2份、盐酸1-3份、37%甲醛水溶液3-5份、对甲基苯胺8-10份、40%烧碱水溶液1-2份、水200-220份;
①按配比将水和磷酸氢二钠放入搅拌槽中,在不断搅拌下升温至60℃,使得磷酸氢二钠溶液完全溶解,按配比将玉米淀粉和磷酸氢二钠溶液充分混合后加入反应器中,物料在反应器中搅拌升温70-80℃,当水量减少到20%以下时,升温至150-200℃,使淀粉与磷酸氢二钠进行反应,当物料的黏度大于50Pa·s时,终止反应,降温出料,即得磷酸酯淀粉;
②将苯酚和醋酸乙烯混合;
③将②中的混合后的溶剂与步骤1中的磷酸酯淀粉加入到瓶中,搅拌,5-9小时;
④再升温,加入十二烷基苯磺酸钠盐、OP-10、过硫酸钾、邻苯二甲酸二丁酯、盐酸、37%甲醛水溶液、对甲基苯胺、40%烧碱水溶液,加热搅拌,加热温度为190℃,时长10分钟;
⑤然后用经双螺杆挤出机挤出、水冷、切割后制得双降解母料,最后经吹膜机吹膜薄膜;
2)纤维层的制备:磷酸氢二钠15-20份、玉米淀粉100-150份、苯酚99-109份、甲醛101-120份、烧碱8-10份、尿素120-150份、氢氧化铵15-25份、水200-220份;
①按配比将水和磷酸氢二钠放入搅拌槽中,在不断搅拌下升温至60℃,使得磷酸氢二钠溶液完全溶解,按配比将玉米淀粉和磷酸氢二钠溶液充分混合后加入反应器中,物料在反应器中搅拌升温70-80℃,当水量减少到20%以下时,升温至150-200℃,使淀粉与磷酸氢二钠进行反应,当物料的黏度大于50Pa·s时,终止反应,降温出料,即得磷酸酯淀粉。
②将甲醛和苯酚混合;
③将②中的混合后的溶剂与步骤1中的磷酸酯淀粉加入到瓶中,搅拌,5-9小时;
④再升温,加入烧碱和尿素,在90-100℃下保持反应1小时;
⑤加入对氢氧化铵调节PH值6-7,终止反应,降温;
⑥然后用经双螺杆挤出机挤出、水冷、切割后制得双降解母料;
将双降解母料熔融后通过气流牵伸纺丝制成网状的长纤维层;将短纤维制成短纤维层;
3)纤维硬化:聚乙烯醇15-20份、蒸馏水130-150份、十二烷基苯磺酸钠盐2-5份、OP-101-3份、过硫酸钾1-2份醋酸乙烯160-180份、邻苯二甲酸二丁酯1-2份、37%甲醛水溶液3-5份;
将聚乙烯醇、OP-10、十二烷基苯磺酸钠盐、过硫酸钾加入搅拌器中,搅拌10分钟,得到搅拌混合溶液;将蒸馏水倒入搅拌罐中,加温,温度控制在60-70℃,10-20分钟,至水与搅拌混合溶液完全溶解;再次加温,温度控制在70-80℃,加温30分钟;加入醋酸乙烯,维持加温反应4小时,再加入37%的甲醛水溶液,得到半成品;最后将邻苯二甲酸二丁酯加入半成品内,搅拌混合得到,制备完成后通过毛刷刷在纤维层上;
4)胶水的制备:端羟基二甲基硅橡胶:45-50份,二酰氧庚烷二丁基锡:0.1-0.2份,气相法白炭黑:10-15份,丁胺:5-10份,甲基三硅烷:1-2份,交联剂:1-2份,催化剂:1-2份,增粘剂:1-2份;
取20-30份端羟基二甲基硅橡胶,与交联剂、催化剂、增粘剂与5-7份气相法白炭黑混合得到A胶剂;
取剩余的端羟基二甲基硅橡胶和余下的气相法白炭黑与丁胺混合得到B胶剂;
将A与B胶剂混合,在20℃的空气中硫化3-5天,使用前60℃加热即可使用;
5)无纺布的合成:将长纤维层附在薄膜上方,短纤维层附在薄膜下方,中间涂上胶水,通过热压,完成合成。
本发明的有益效果是:本发明所采用的淀粉来源丰富、价格低廉,对环境友好;并且制得的无纺布强度高、生产成本低、可生物降解,能有效缓解白色污染问题,存放时间长,耐高温,耐水,延长使用寿命,减少白色污染,保护环境。
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,下面结合具体实施例,进一步阐述本发明。
具体实施例:一种防断裂无纺布的制备方法,包括:
1)薄膜的制备:磷酸氢二钠15份、玉米淀粉100份、苯酚15份、十二烷基苯磺酸钠盐2-份、OP-101份、过硫酸钾1份醋酸乙烯160份、邻苯二甲酸二丁酯1份、盐酸1份、37%甲醛水溶液3份、对甲基苯胺8份、40%烧碱水溶液1份、水200份;
①按配比将水和磷酸氢二钠放入搅拌槽中,在不断搅拌下升温至60℃,使得磷酸氢二钠溶液完全溶解,按配比将玉米淀粉和磷酸氢二钠溶液充分混合后加入反应器中,物料在反应器中搅拌升温70-80℃,当水量减少到20%以下时,升温至150-200℃,使淀粉与磷酸氢二钠进行反应,当物料的黏度大于50Pa·s时,终止反应,降温出料,即得磷酸酯淀粉;
②将苯酚和醋酸乙烯混合;
③将②中的混合后的溶剂与步骤1中的磷酸酯淀粉加入到瓶中,搅拌,5-9小时;
④再升温,加入十二烷基苯磺酸钠盐、OP-10、过硫酸钾、邻苯二甲酸二丁酯、盐酸、37%甲醛水溶液、对甲基苯胺、40%烧碱水溶液,加热搅拌,加热温度为190℃,时长10分钟;
⑤然后用经双螺杆挤出机挤出、水冷、切割后制得双降解母料,最后经吹膜机吹膜薄膜;
2)纤维层的制备:磷酸氢二钠15份、玉米淀粉100份、苯酚99份、甲醛101份、烧碱8份、尿素120份、氢氧化铵15份、水200份;
①按配比将水和磷酸氢二钠放入搅拌槽中,在不断搅拌下升温至60℃,使得磷酸氢二钠溶液完全溶解,按配比将玉米淀粉和磷酸氢二钠溶液充分混合后加入反应器中,物料在反应器中搅拌升温70-80℃,当水量减少到20%以下时,升温至150-200℃,使淀粉与磷酸氢二钠进行反应,当物料的黏度大于50Pa·s时,终止反应,降温出料,即得磷酸酯淀粉。
②将甲醛和苯酚混合;
③将②中的混合后的溶剂与步骤1中的磷酸酯淀粉加入到瓶中,搅拌,5-9小时;
④再升温,加入烧碱和尿素,在90-100℃下保持反应1小时;
⑤加入对氢氧化铵调节PH值6-7,终止反应,降温;
⑥然后用经双螺杆挤出机挤出、水冷、切割后制得双降解母料;
将双降解母料熔融后通过气流牵伸纺丝制成网状的长纤维层;将短纤维制成短纤维层;
3)纤维硬化:聚乙烯醇15份、蒸馏水130份、十二烷基苯磺酸钠盐2份、OP-101份、过硫酸钾1份醋酸乙烯160份、邻苯二甲酸二丁酯1份、37%甲醛水溶液3份;
将聚乙烯醇、OP-10、十二烷基苯磺酸钠盐、过硫酸钾加入搅拌器中,搅拌10分钟,得到搅拌混合溶液;将蒸馏水倒入搅拌罐中,加温,温度控制在60-70℃,10-20分钟,至水与搅拌混合溶液完全溶解;再次加温,温度控制在70-80℃,加温30分钟;加入醋酸乙烯,维持加温反应4小时,再加入37%的甲醛水溶液,得到半成品;最后将邻苯二甲酸二丁酯加入半成品内,搅拌混合得到,制备完成后通过毛刷刷在纤维层上;
4)胶水的制备:端羟基二甲基硅橡胶:45份,二酰氧庚烷二丁基锡:0.1份,气相法白炭黑:10份,丁胺:5份,甲基三硅烷:1份,交联剂:1份,催化剂:1份,增粘剂:1份;
取20-30份端羟基二甲基硅橡胶,与交联剂、催化剂、增粘剂与5份气相法白炭黑混合得到A胶剂;
取剩余的端羟基二甲基硅橡胶和余下的气相法白炭黑与丁胺混合得到B胶剂;
将A与B胶剂混合,在20℃的空气中硫化3-5天,使用前60℃加热即可使用;
5)无纺布的合成:将长纤维层附在薄膜上方,短纤维层附在薄膜下方,中间涂上胶水,通过热压,完成合成。
实施例二:一种防断裂无纺布的制备方法,包括:
1)薄膜的制备:磷酸氢二钠20份、玉米淀粉150份、苯酚20份、十二烷基苯磺酸钠盐5份、OP-103份、过硫酸钾2份醋酸乙烯180份、邻苯二甲酸二丁酯2份、盐酸3份、37%甲醛水溶液5份、对甲基苯胺10份、40%烧碱水溶液2份、水220份;
①按配比将水和磷酸氢二钠放入搅拌槽中,在不断搅拌下升温至60℃,使得磷酸氢二钠溶液完全溶解,按配比将玉米淀粉和磷酸氢二钠溶液充分混合后加入反应器中,物料在反应器中搅拌升温70-80℃,当水量减少到20%以下时,升温至150-200℃,使淀粉与磷酸氢二钠进行反应,当物料的黏度大于50Pa·s时,终止反应,降温出料,即得磷酸酯淀粉;
②将苯酚和醋酸乙烯混合;
③将②中的混合后的溶剂与步骤1中的磷酸酯淀粉加入到瓶中,搅拌,5-9小时;
④再升温,加入十二烷基苯磺酸钠盐、OP-10、过硫酸钾、邻苯二甲酸二丁酯、盐酸、37%甲醛水溶液、对甲基苯胺、40%烧碱水溶液,加热搅拌,加热温度为190℃,时长10分钟;
⑤然后用经双螺杆挤出机挤出、水冷、切割后制得双降解母料,最后经吹膜机吹膜薄膜;
2)纤维层的制备:磷酸氢二钠20份、玉米淀粉150份、苯酚109份、甲醛120份、烧碱10份、尿素150份、氢氧化铵25份、水220份;
①按配比将水和磷酸氢二钠放入搅拌槽中,在不断搅拌下升温至60℃,使得磷酸氢二钠溶液完全溶解,按配比将玉米淀粉和磷酸氢二钠溶液充分混合后加入反应器中,物料在反应器中搅拌升温70-80℃,当水量减少到20%以下时,升温至150-200℃,使淀粉与磷酸氢二钠进行反应,当物料的黏度大于50Pa·s时,终止反应,降温出料,即得磷酸酯淀粉。
②将甲醛和苯酚混合;
③将②中的混合后的溶剂与步骤1中的磷酸酯淀粉加入到瓶中,搅拌,5-9小时;
④再升温,加入烧碱和尿素,在90-100℃下保持反应1小时;
⑤加入对氢氧化铵调节PH值6-7,终止反应,降温;
⑥然后用经双螺杆挤出机挤出、水冷、切割后制得双降解母料;
将双降解母料熔融后通过气流牵伸纺丝制成网状的长纤维层;将短纤维制成短纤维层;
3)纤维硬化:聚乙烯醇20份、蒸馏水150份、十二烷基苯磺酸钠盐5份、OP-103份、过硫酸钾2份醋酸乙烯180份、邻苯二甲酸二丁酯2份、37%甲醛水溶液5份;
将聚乙烯醇、OP-10、十二烷基苯磺酸钠盐、过硫酸钾加入搅拌器中,搅拌10分钟,得到搅拌混合溶液;将蒸馏水倒入搅拌罐中,加温,温度控制在60-70℃,10-20分钟,至水与搅拌混合溶液完全溶解;再次加温,温度控制在70-80℃,加温30分钟;加入醋酸乙烯,维持加温反应4小时,再加入37%的甲醛水溶液,得到半成品;最后将邻苯二甲酸二丁酯加入半成品内,搅拌混合得到,制备完成后通过毛刷刷在纤维层上;
4)胶水的制备:端羟基二甲基硅橡胶:50份,二酰氧庚烷二丁基锡:0.2份,气相法白炭黑:15份,丁胺:10份,甲基三硅烷:2份,交联剂:2份,催化剂:2份,增粘剂:2份;
取20-30份端羟基二甲基硅橡胶,与交联剂、催化剂、增粘剂与7份气相法白炭黑混合得到A胶剂;
取剩余的端羟基二甲基硅橡胶和余下的气相法白炭黑与丁胺混合得到B胶剂;
将A与B胶剂混合,在20℃的空气中硫化3-5天,使用前60℃加热即可使用;
5)无纺布的合成:将长纤维层附在薄膜上方,短纤维层附在薄膜下方,中间涂上胶水,通过热压,完成合成。
以上显示和描述了本发明的基本原理、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 (1)
1.一种防断裂无纺布的制备方法,其特征在于:包括:
1)薄膜的制备:磷酸氢二钠15-20份、玉米淀粉100-150份、苯酚15-20份、十二烷基苯磺酸钠盐2-5份、OP-101-3份、过硫酸钾1-2份醋酸乙烯160-180份、邻苯二甲酸二丁酯1-2份、盐酸1-3份、37%甲醛水溶液3-5份、对甲基苯胺8-10份、40%烧碱水溶液1-2份、水200-220份;
①按配比将水和磷酸氢二钠放入搅拌槽中,在不断搅拌下升温至60℃,使得磷酸氢二钠溶液完全溶解,按配比将玉米淀粉和磷酸氢二钠溶液充分混合后加入反应器中,物料在反应器中搅拌升温70-80℃,当水量减少到20%以下时,升温至150-200℃,使淀粉与磷酸氢二钠进行反应,当物料的黏度大于50Pa·s时,终止反应,降温出料,即得磷酸酯淀粉;
②将苯酚和醋酸乙烯混合;
③将②中的混合后的溶剂与步骤1中的磷酸酯淀粉加入到瓶中,搅拌,5-9小时;
④再升温,加入十二烷基苯磺酸钠盐、OP-10、过硫酸钾、邻苯二甲酸二丁酯、盐酸、37%甲醛水溶液、对甲基苯胺、40%烧碱水溶液,加热搅拌,加热温度为190℃,时长10分钟;
⑤然后用经双螺杆挤出机挤出、水冷、切割后制得双降解母料,最后经吹膜机吹膜薄膜;
2)纤维层的制备:磷酸氢二钠15-20份、玉米淀粉100-150份、苯酚99-109份、甲醛101-120份、烧碱8-10份、尿素120-150份、氢氧化铵15-25份、水200-220份;
①按配比将水和磷酸氢二钠放入搅拌槽中,在不断搅拌下升温至60℃,使得磷酸氢二钠溶液完全溶解,按配比将玉米淀粉和磷酸氢二钠溶液充分混合后加入反应器中,物料在反应器中搅拌升温70-80℃,当水量减少到20%以下时,升温至150-200℃,使淀粉与磷酸氢二钠进行反应,当物料的黏度大于50Pa·s时,终止反应,降温出料,即得磷酸酯淀粉。
②将甲醛和苯酚混合;
③将②中的混合后的溶剂与步骤1中的磷酸酯淀粉加入到瓶中,搅拌,5-9小时;
④再升温,加入烧碱和尿素,在90-100℃下保持反应1小时;
⑤加入对氢氧化铵调节PH值6-7,终止反应,降温;
⑥然后用经双螺杆挤出机挤出、水冷、切割后制得双降解母料;
将双降解母料熔融后通过气流牵伸纺丝制成网状的长纤维层;将短纤维制成短纤维层;
3)纤维硬化:聚乙烯醇15-20份、蒸馏水130-150份、十二烷基苯磺酸钠盐2-5份、OP-101-3份、过硫酸钾1-2份醋酸乙烯160-180份、邻苯二甲酸二丁酯1-2份、37%甲醛水溶液3-5份;
将聚乙烯醇、OP-10、十二烷基苯磺酸钠盐、过硫酸钾加入搅拌器中,搅拌10分钟,得到搅拌混合溶液;将蒸馏水倒入搅拌罐中,加温,温度控制在60-70℃,10-20分钟,至水与搅拌混合溶液完全溶解;再次加温,温度控制在70-80℃,加温30分钟;加入醋酸乙烯,维持加温反应4小时,再加入37%的甲醛水溶液,得到半成品;最后将邻苯二甲酸二丁酯加入半成品内,搅拌混合得到,制备完成后通过毛刷刷在纤维层上;
4)胶水的制备:端羟基二甲基硅橡胶:45-50份,二酰氧庚烷二丁基锡:0.1-0.2份,气相法白炭黑:10-15份,丁胺:5-10份,甲基三硅烷:1-2份,交联剂:1-2份,催化剂:1-2份,增粘剂:1-2份;
取20-30份端羟基二甲基硅橡胶,与交联剂、催化剂、增粘剂与5-7份气相法白炭黑混合得到A胶剂;
取剩余的端羟基二甲基硅橡胶和余下的气相法白炭黑与丁胺混合得到B胶剂;
将A与B胶剂混合,在20℃的空气中硫化3-5天,使用前60℃加热即可使用;
5)无纺布的合成:将长纤维层附在薄膜上方,短纤维层附在薄膜下方,中间涂上胶水,通过热压,完成合成。
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| EP1101855A1 (en) * | 1999-11-17 | 2001-05-23 | Nippon Petrochemicals Company, Limited | Cross laminated nonwoven fabric having intermediate layer |
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| CN1072223A (zh) * | 1991-11-07 | 1993-05-19 | 埃姆斯-英维塔公司 | 淀粉纤维、其制造方法及用途 |
| EP1101855A1 (en) * | 1999-11-17 | 2001-05-23 | Nippon Petrochemicals Company, Limited | Cross laminated nonwoven fabric having intermediate layer |
| CN1431362A (zh) * | 2003-01-15 | 2003-07-23 | 李彦亭 | 聚乙烯醇缩醛浸塑布及用途 |
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