CN116855165A - 高性能聚氨酯防水涂料 - Google Patents
高性能聚氨酯防水涂料 Download PDFInfo
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- CN116855165A CN116855165A CN202310867057.0A CN202310867057A CN116855165A CN 116855165 A CN116855165 A CN 116855165A CN 202310867057 A CN202310867057 A CN 202310867057A CN 116855165 A CN116855165 A CN 116855165A
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- 229920002635 polyurethane Polymers 0.000 title claims abstract description 43
- 239000004814 polyurethane Substances 0.000 title claims abstract description 43
- 239000003973 paint Substances 0.000 title claims description 12
- 239000004721 Polyphenylene oxide Substances 0.000 claims abstract description 59
- 229920000570 polyether Polymers 0.000 claims abstract description 59
- 229920005862 polyol Polymers 0.000 claims abstract description 59
- 150000003077 polyols Chemical class 0.000 claims abstract description 59
- 238000000576 coating method Methods 0.000 claims abstract description 34
- 239000011248 coating agent Substances 0.000 claims abstract description 30
- HLDBBQREZCVBMA-UHFFFAOYSA-N hydroxy-tris[(2-methylpropan-2-yl)oxy]silane Chemical compound CC(C)(C)O[Si](O)(OC(C)(C)C)OC(C)(C)C HLDBBQREZCVBMA-UHFFFAOYSA-N 0.000 claims abstract description 12
- RKISUIUJZGSLEV-UHFFFAOYSA-N n-[2-(octadecanoylamino)ethyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCNC(=O)CCCCCCCCCCCCCCCCC RKISUIUJZGSLEV-UHFFFAOYSA-N 0.000 claims abstract description 11
- 229920000805 Polyaspartic acid Polymers 0.000 claims abstract description 8
- 150000002148 esters Chemical class 0.000 claims abstract description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 8
- 239000004014 plasticizer Substances 0.000 claims abstract description 8
- 108010064470 polyaspartate Proteins 0.000 claims abstract description 8
- 239000004925 Acrylic resin Substances 0.000 claims abstract description 7
- 229920000178 Acrylic resin Polymers 0.000 claims abstract description 7
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 7
- 125000005442 diisocyanate group Chemical group 0.000 claims abstract description 7
- 239000002904 solvent Substances 0.000 claims abstract description 7
- 239000006087 Silane Coupling Agent Substances 0.000 claims abstract description 6
- 239000000945 filler Substances 0.000 claims abstract description 4
- 230000000379 polymerizing effect Effects 0.000 claims abstract description 3
- 238000006243 chemical reaction Methods 0.000 claims description 7
- 238000002360 preparation method Methods 0.000 claims description 6
- YEVQZPWSVWZAOB-UHFFFAOYSA-N 2-(bromomethyl)-1-iodo-4-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=CC=C(I)C(CBr)=C1 YEVQZPWSVWZAOB-UHFFFAOYSA-N 0.000 claims description 5
- 238000001816 cooling Methods 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 5
- 238000002156 mixing Methods 0.000 claims description 5
- 238000003756 stirring Methods 0.000 claims description 5
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Natural products OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 4
- FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 claims description 3
- 239000005057 Hexamethylene diisocyanate Substances 0.000 claims description 3
- XBXFGOSIPGWNLZ-UHFFFAOYSA-N O=C1C=C(CC(C)(C)C1)C.N=C=O Chemical compound O=C1C=C(CC(C)(C)C1)C.N=C=O XBXFGOSIPGWNLZ-UHFFFAOYSA-N 0.000 claims description 3
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 claims description 2
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 claims description 2
- -1 citric acid ester Chemical class 0.000 claims description 2
- 239000012948 isocyanate Substances 0.000 claims description 2
- 150000002513 isocyanates Chemical class 0.000 claims description 2
- 230000035484 reaction time Effects 0.000 claims description 2
- 230000006750 UV protection Effects 0.000 abstract description 11
- 239000000463 material Substances 0.000 abstract description 9
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- 239000000843 powder Substances 0.000 description 5
- 230000018044 dehydration Effects 0.000 description 4
- 238000006297 dehydration reaction Methods 0.000 description 4
- OUPZKGBUJRBPGC-UHFFFAOYSA-N 1,3,5-tris(oxiran-2-ylmethyl)-1,3,5-triazinane-2,4,6-trione Chemical compound O=C1N(CC2OC2)C(=O)N(CC2OC2)C(=O)N1CC1CO1 OUPZKGBUJRBPGC-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000010453 quartz Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
- 239000012752 auxiliary agent Substances 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000010445 mica Substances 0.000 description 2
- 229910052618 mica group Inorganic materials 0.000 description 2
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229920001730 Moisture cure polyurethane Polymers 0.000 description 1
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229940037312 stearamide Drugs 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
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- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
- C09D175/08—Polyurethanes from polyethers
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- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
- C08G18/12—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step using two or more compounds having active hydrogen in the first polymerisation step
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- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
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- C08G18/755—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group containing one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group having a primary carbon atom next to the isocyanate or isothiocyanate group and at least one isocyanate or isothiocyanate group linked to a secondary carbon atom of the cycloaliphatic ring, e.g. isophorone diisocyanate
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Abstract
本发明涉及防水涂料技术领域,提出了一种高性能聚氨酯防水涂料,由A组分和B组分组成,其中A组分为聚醚多元醇和二异氰酸酯聚合得到的预聚体;B组分由以下重量份组分组成:45‑50份羟基丙烯酸树脂、4‑8份改性聚天门冬氨酸酯、4‑10份增塑剂、0.5‑0.8份固化剂、5‑10份填料、0.1‑0.3份硅烷偶联剂、0.3‑0.5份三叔丁氧基硅醇、0.6‑1份乙撑基双硬脂酰胺、30‑40份溶剂。通过上述技术方案,解决了现有技术中聚氨酯防水材料脆性大,耐紫外线性能差的问题。
Description
技术领域
本发明涉及防水涂料技术领域,具体的,涉及一种高性能聚氨酯防水涂料。
背景技术
聚氨酯防水涂料是以聚氨酯树脂为主要成膜物质的一类高分子防水材料,是由异氧酸酯基(-NCO)的聚氨酯预聚体和含有多羟基(-OH)或氨基(-NH2)的固化剂以及其他助剂的混合物按一定比例混合形成的一种反应型涂膜防水材料。
聚氨酯防水涂料在建筑防水中应用广泛,可适用于各种屋面防水工程,如地下建筑防水工程,浴室、卫生间防水工程,地下管道防水等室内或地下防水和高速、铁路、无砟轨道、桥面等室外防水。
但是,聚氨酯防水材料固化后,聚氨酯材料偏脆,缺乏弹性,因此,为了提高涂层的柔性问题,一般采用添加增塑剂的方式来提高涂层的柔性,但添加的增塑剂在阳光下长久暴晒会出现迁移,增塑剂迁移后涂层的脆性会增加,导致聚氨酯防水涂料的性能下降,缩短聚氨酯防水涂料的使用寿命。
发明内容
本发明提出一种高性能聚氨酯防水涂料,解决了相关技术中的聚氨酯防水材料脆性大,耐紫外线性能差的问题。
本发明的技术方案如下:
一种高性能聚氨酯防水涂料,由A组分和B组分组成,其中A组分为聚醚多元醇和二异氰酸酯聚合得到的预聚体;B组分由以下重量份组分组成:45-50份羟基丙烯酸树脂、4-8份改性聚天门冬氨酸酯、4-10份增塑剂、0.5-0.8份固化剂、5-10份填料、0.1-0.3份硅烷偶联剂、0.3-0.5份三叔丁氧基硅醇、0.6-1份乙撑基双硬脂酰胺、30-40份溶剂。
作为进一步技术方案,所述二异氰酸酯包括异佛尔酮异氰酸酯、六亚甲基二异氰酸酯、苯二亚甲基二异氰酸酯中的一种。
作为进一步技术方案,所述填料包括沉淀硫酸钡、石英粉、云母粉中的一种或多种。
作为进一步技术方案,所述聚醚多元醇由低分子量聚醚多元醇和高分子量聚醚多元醇组成;所述低分子量聚醚多元醇分子量为400,所述高分子量聚醚多元醇分子量为1000-3000。
作为进一步技术方案,所述,所述高分子量聚醚多元醇分子量为2000。
作为进一步技术方案,所述低分子量聚醚多元醇和高分子量聚醚多元醇的质量比为1:0.5-1.5。
作为进一步技术方案,所述低分子量聚醚多元醇和高分子量聚醚多元醇的质量比为1:1。
作为进一步技术方案,所述预聚体的制备方法为:将聚醚多元醇投入反应釜中,搅拌升温至100-105℃,脱水,然后降温至50-60℃后,加入异氰酸酯,反应后,得到预聚体。
作为进一步技术方案,所述脱水为真空脱水,脱水压力为-0.08~-0.1MPa,脱水时间为2-3h。
作为进一步技术方案,所述反应温度为80-85℃,反应时间为2-5h。
作为进一步技术方案,所述聚醚多元醇和二异氰酸酯的质量比为50-75:25-50。
作为进一步技术方案,所述增塑剂为磷酸三辛酯、柠檬酸酯、邻苯二甲酸二辛酯中的一种或多种。
本发明还包括一种高性能聚氨酯防水涂料的制备方法,包括以下步骤:将A组分与B组分按比例混合得到。
作为进一步技术方案,所述A组分与B组分的质量比为1:1-3。
作为进一步技术方案,所述溶剂为甲苯、二甲苯、醋酸丁酯、醋酸乙酯、丁酮、丙酮、乙二醇乙醚醋酸酯中的一种或多种。
本发明的工作原理及有益效果为:
1、本发明中聚氨酯防水涂料由A组分和B组分组成,B组分以羟基丙烯酸树脂和改性聚天门冬氨酸酯为基料树脂,并添加三叔丁氧基硅醇、乙撑基双硬脂酰胺作为助剂,不仅提高了聚氨酯防水涂料的分散性,还提高了耐紫外线性能,提高了聚氨酯防水涂料的使用寿命。
2、本发明中,A组分中聚醚多元醇由低分子量聚醚多元醇和高分子量聚醚多元醇组成,通过优化低分子量聚醚多元醇和高分子量聚醚多元醇的分子量和配比,使得本发明中制备的聚氨酯防水涂料具有较高的拉伸强度和耐紫外线性能。
具体实施方式
下面将结合本发明实施例,对本发明实施例中的技术方案进行清楚、完整地描述,显然,所描述的实施例仅仅是本发明一部分实施例,而不是全部的实施例。基于本发明中的实施例,本领域普通技术人员在没有作出创造性劳动前提下所获得的所有其他实施例,都涉及本发明保护的范围。
下述实施例及对比例中:
DL-400聚醚多元醇,分子量为400;DL-1000D聚醚多元醇,分子量为1000;DL-2000D聚醚多元醇,分子量为2000;DL-3000D聚醚多元醇,分子量为3000,上述均购自广州永仕化工有限公司;改性聚天门冬氨酸酯F524,购自飞扬新材料股份有限公司。
实施例1
高性能聚氨酯防水涂料的制备方法,包括以下步骤:
S1、将25份DL-400聚醚多元醇、25份DL-2000D聚醚多元醇投入反应釜中,搅拌升温至100℃,在-0.08-MPa下脱水-3h,然后降温至50℃后,加入25份异佛尔酮异氰酸酯,在80℃,反应5h,得到预聚体,即为A组分;
S2、将45份羟基丙烯酸树脂、4份改性聚天门冬氨酸酯F524、4份磷酸三辛酯、0.5份TGIC固化剂、5份石英粉、0.1份硅烷偶联剂KH-550、0.3份三叔丁氧基硅醇、0.6份乙撑基双硬脂酰胺、30份溶剂,加入到高速分散机中分散均匀,得到B组分;
S3、取上述制备的10份A组分和10份B组分混合后,得到聚氨酯防水涂料。
实施例2
高性能聚氨酯防水涂料的制备方法,包括以下步骤:
S1、将30份DL-400聚醚多元醇、30份DL-2000D聚醚多元醇投入反应釜中,搅拌升温至1020-105℃,在-0.09Pa下脱水2.5h,然后降温至55℃后,加入40份六亚甲基二异氰酸酯,在80-85℃,反应2-5h,得到预聚体,即为A组分;
S2、将47份羟基丙烯酸树脂、6份改性聚天门冬氨酸酯F524、6份磷酸三辛酯、0.7份TGIC固化剂、8份石英粉、0.2份硅烷偶联剂KH-550、0.4份三叔丁氧基硅醇、0.8份乙撑基双硬脂酰胺、35份溶剂,加入到高速分散机中分散均匀,得到B组分;
S3、取上述制备的10份A组分和20份B组分混合后,得到聚氨酯防水涂料。
实施例3
高性能聚氨酯防水涂料的制备方法,包括以下步骤:
S1、将37.5份DL-400聚醚多元醇、37.5份DL-2000D聚醚多元醇投入反应釜中,搅拌升温至105℃,在-0.1MPa下脱水2h,然后降温至60℃后,加入50份苯二亚甲基二异氰酸酯,在85℃,反应2h,得到预聚体,即为A组分;
S2、50份羟基丙烯酸树脂、8份改性聚天门冬氨酸酯F524、10份磷酸三辛酯、0.8份TGIC固化剂、10份云母粉、0.3份硅烷偶联剂KH-550、0.5份三叔丁氧基硅醇、1份乙撑基双硬脂酰胺、40份溶剂,加入到高速分散机中分散均匀,得到B组分;
S3、取上述制备的10份A组分和30份B组分混合后,得到聚氨酯防水涂料。
实施例4
与实施例1相比,实施例4的不同之处在于,30份DL-400聚醚多元醇、20份DL-2000D聚醚多元醇。
实施例5
与实施例1相比,实施例5的不同之处在于,20份DL-400聚醚多元醇、30份DL-2000D聚醚多元醇。
实施例6
与实施例1相比,实施例6将DL-2000D聚醚多元醇替换成等量的DL-1000D,其他与实施例1相同。
实施例7
与实施例1相比,实施例7将DL-2000D聚醚多元醇替换成等量的DL-3000D,其他与实施例1相同。
对比例1
与实施例1相比,对比例1将DL-2000D聚醚多元醇替换成等量的DL-400聚醚多元醇,其他与实施例1相同。
对比例2
与实施例1相比,对比例2将DL-400聚醚多元醇替换成等量的DL-2000D聚醚多元醇,其他与实施例1相同。
对比例3
与实施例1相比,对比例3不添加三叔丁氧基硅醇,其他与实施例1相同。
对比例4
与实施例1相比,对比例4不添加乙撑基双硬脂酰胺,其他与实施例1相同。
对比例5
与实施例1相比,对比例5不添加三叔丁氧基硅醇和乙撑基双硬脂酰胺,其他与实施例1相同。
试验例
测定实施例1-7及对比例1-5制备得到的聚氨酯防水涂料的拉伸强度和耐紫外线性能,测定方法如下:
依据GB/T 19250-2013《聚氨酯防水涂料》中的方法测定防水涂料的拉伸强度及紫外线处理2000h后的拉伸强度保持率;
测定结果如表1所示。
表1实施例1-7及对比例1-5聚氨酯防水涂料的性能测试结果
与实施例1相比,实施例4-5改变DL-400聚醚多元醇和DL-2000D聚醚多元醇的质量比,实施例6将DL-2000D聚醚多元醇替换成等量的DL-1000D,实施例7将DL-2000D聚醚多元醇替换成等量的DL-3000D,结果实施例4-7制备的聚氨酯防水涂料的拉伸强度和耐紫外线2000h后的拉伸强度保持率低于实施例1,说明DL-400聚醚多元醇和DL-2000D聚醚多元醇的质量比为1:1时制备的拉伸强度和耐紫外线2000h后的拉伸强度保持率最高。
与实施例1相比,对比例1仅使用DL-400聚醚多元醇,对比例2仅使用DL-2000D聚醚多元醇,结果对比例1-2制备的聚氨酯防水涂料的拉伸强度和耐紫外线2000h后的拉伸强度保持率低于实施例1,说明同时使用DL-400聚醚多元醇和DL-2000D聚醚多元醇制备得到的聚氨酯防水涂料的拉伸强度和耐紫外线2000h后的拉伸强度保持率最高。
与实施例1相比,对比例3不添加三叔丁氧基硅醇,对比例4不添加乙撑基双硬脂酰胺,对比例5不添加三叔丁氧基硅醇和乙撑基双硬脂酰胺,结果对比例3-5制备的聚氨酯防水涂料的拉伸强度和耐紫外线2000h后的拉伸强度保持率均低于实施例1,说明同时添加三叔丁氧基硅醇和乙撑基双硬脂酰胺可以提高聚氨酯防水涂料的拉伸强度和耐紫外线2000h后的拉伸强度保持率。
以上仅为本发明的较佳实施例而已,并不用以限制本发明,凡在本发明的精神和原则之内,所作的任何修改、等同替换、改进等,均应包含在本发明的保护范围之内。
Claims (10)
1.一种高性能聚氨酯防水涂料,其特征在于,由A组分和B组分组成,其中A组分为聚醚多元醇和二异氰酸酯聚合得到的预聚体;B组分由以下重量份组分组成:45-50份羟基丙烯酸树脂、4-8份改性聚天门冬氨酸酯、4-10份增塑剂、0.5-0.8份固化剂、5-10份填料、0.1-0.3份硅烷偶联剂、0.3-0.5份三叔丁氧基硅醇、0.6-1份乙撑基双硬脂酰胺、30-40份溶剂。
2.根据权利要求1所述的一种高性能聚氨酯防水涂料,其特征在于,所述二异氰酸酯包括异佛尔酮异氰酸酯、六亚甲基二异氰酸酯、苯二亚甲基二异氰酸酯中的一种。
3.根据权利要求1所述的一种高性能聚氨酯防水涂料,其特征在于,所述聚醚多元醇由低分子量聚醚多元醇和高分子量聚醚多元醇组成;所述低分子量聚醚多元醇分子量为400,所述高分子量聚醚多元醇分子量为1000-3000。
4.根据权利要求3所述的一种高性能聚氨酯防水涂料,其特征在于,所述低分子量聚醚多元醇和高分子量聚醚多元醇的质量比为1:0.5-1.5。
5.根据权利要求1所述的一种高性能聚氨酯防水涂料,其特征在于,所述预聚体的制备方法为:将聚醚多元醇投入反应釜中,搅拌升温至100-105℃,脱水,然后降温至50-60℃后,加入异氰酸酯,反应后,得到预聚体。
6.根据权利要求5所述的一种高性能聚氨酯防水涂料,其特征在于,所述反应温度为80-85℃,反应时间为2-5h。
7.根据权利要求5所述的一种高性能聚氨酯防水涂料,其特征在于,所述聚醚多元醇和二异氰酸酯的质量比为50-75:25-50。
8.根据权利要求1所述的一种高性能聚氨酯防水涂料,其特征在于,所述增塑剂为磷酸三辛酯、柠檬酸酯、邻苯二甲酸二辛酯中的一种或多种。
9.根据权利要求1所述的一种高性能聚氨酯防水涂料的制备方法,其特征在于,包括以下步骤:将A组分与B组分按比例混合得到。
10.根据权利要求9所述的一种高性能聚氨酯防水涂料的制备方法,其特征在于,所述A组分与B组分的质量比为1:1-3。
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