CN116855165A - 高性能聚氨酯防水涂料 - Google Patents

高性能聚氨酯防水涂料 Download PDF

Info

Publication number
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
Authority
CN
China
Prior art keywords
polyether polyol
parts
component
polyurethane waterproof
molecular weight
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN202310867057.0A
Other languages
English (en)
Inventor
郭志铅
纪刚
苏学锦
孙策
刘伟光
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hebei Jinkun Engineering Material Co ltd
Original Assignee
Hebei Jinkun Engineering Material Co ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hebei Jinkun Engineering Material Co ltd filed Critical Hebei Jinkun Engineering Material Co ltd
Priority to CN202310867057.0A priority Critical patent/CN116855165A/zh
Publication of CN116855165A publication Critical patent/CN116855165A/zh
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D175/00Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04Polyurethanes
    • C09D175/08Polyurethanes from polyethers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08Processes
    • C08G18/10Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
    • C08G18/12Prepolymer 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
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/4009Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
    • C08G18/4081Mixtures of compounds of group C08G18/64 with other macromolecular compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/48Polyethers
    • C08G18/4804Two or more polyethers of different physical or chemical nature
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/62Polymers of compounds having carbon-to-carbon double bonds
    • C08G18/6216Polymers of alpha-beta ethylenically unsaturated carboxylic acids or of derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/63Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/64Macromolecular compounds not provided for by groups C08G18/42 - C08G18/63
    • C08G18/6415Macromolecular compounds not provided for by groups C08G18/42 - C08G18/63 having nitrogen
    • C08G18/6438Polyimides or polyesterimides
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/74Polyisocyanates or polyisothiocyanates cyclic
    • C08G18/75Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic
    • C08G18/751Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring
    • C08G18/752Polyisocyanates 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
    • C08G18/753Polyisocyanates 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
    • C08G18/755Polyisocyanates 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
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/74Polyisocyanates or polyisothiocyanates cyclic
    • C08G18/76Polyisocyanates or polyisothiocyanates cyclic aromatic
    • C08G18/7614Polyisocyanates or polyisothiocyanates cyclic aromatic containing only one aromatic ring
    • C08G18/7628Polyisocyanates or polyisothiocyanates cyclic aromatic containing only one aromatic ring containing at least one isocyanate or isothiocyanate group linked to the aromatic ring by means of an aliphatic group
    • C08G18/7635Polyisocyanates or polyisothiocyanates cyclic aromatic containing only one aromatic ring containing at least one isocyanate or isothiocyanate group linked to the aromatic ring by means of an aliphatic group containing one isocyanate or isothiocyanate group linked to the aromatic ring by means of an aliphatic group and at least one isocyanate or isothiocyanate group directly linked to the aromatic ring, e.g. isocyanatobenzylisocyanate
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/60Additives non-macromolecular
    • C09D7/61Additives non-macromolecular inorganic
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/60Additives non-macromolecular
    • C09D7/63Additives non-macromolecular organic

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Inorganic Chemistry (AREA)
  • Paints Or Removers (AREA)

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

高性能聚氨酯防水涂料
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。
CN202310867057.0A 2023-07-14 2023-07-14 高性能聚氨酯防水涂料 Pending CN116855165A (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202310867057.0A CN116855165A (zh) 2023-07-14 2023-07-14 高性能聚氨酯防水涂料

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202310867057.0A CN116855165A (zh) 2023-07-14 2023-07-14 高性能聚氨酯防水涂料

Publications (1)

Publication Number Publication Date
CN116855165A true CN116855165A (zh) 2023-10-10

Family

ID=88235624

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202310867057.0A Pending CN116855165A (zh) 2023-07-14 2023-07-14 高性能聚氨酯防水涂料

Country Status (1)

Country Link
CN (1) CN116855165A (zh)

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103805048A (zh) * 2014-03-04 2014-05-21 大连怿文新材料科技发展有限公司 景观道具用聚天门冬氨酸酯防护涂料及其制备方法
CN103865029A (zh) * 2012-12-11 2014-06-18 哈尔滨六环涂料化工有限公司 一种聚氨酯防水涂料预聚体的制备方法
CN104140755A (zh) * 2014-07-27 2014-11-12 北京东方雨虹防水技术股份有限公司 一种环保型弹性耐候型丙烯酸聚氨酯涂料、制备及应用
CN105295702A (zh) * 2015-11-23 2016-02-03 北京航玻新材料技术有限公司 弹性涂料及其制备方法
CN109554101A (zh) * 2018-11-15 2019-04-02 唐山东方雨虹防水技术有限责任公司 一种聚氨酯防水涂料
CN109761834A (zh) * 2019-03-05 2019-05-17 郁维铭 一种水可分散的聚天门冬氨酸酯树脂及水性聚脲涂料的制备方法和应用
CN112980312A (zh) * 2021-03-05 2021-06-18 亚士防水科技(滁州)有限公司 双组份聚氨酯防水涂料及其制备方法
CN114350250A (zh) * 2022-02-21 2022-04-15 中南大学 一种基于刺激响应方式的快干生物基水性聚氨酯涂料及其制备方法
CN114907761A (zh) * 2022-06-24 2022-08-16 安徽尚德轨道设备制造有限公司 一种非固化丙烯酸改性聚氨酯防水涂料
CN115536984A (zh) * 2022-11-24 2022-12-30 河北坤鹏光电科技有限公司 一种硅橡胶内置胶泥冷缩套管

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103865029A (zh) * 2012-12-11 2014-06-18 哈尔滨六环涂料化工有限公司 一种聚氨酯防水涂料预聚体的制备方法
CN103805048A (zh) * 2014-03-04 2014-05-21 大连怿文新材料科技发展有限公司 景观道具用聚天门冬氨酸酯防护涂料及其制备方法
CN104140755A (zh) * 2014-07-27 2014-11-12 北京东方雨虹防水技术股份有限公司 一种环保型弹性耐候型丙烯酸聚氨酯涂料、制备及应用
CN105295702A (zh) * 2015-11-23 2016-02-03 北京航玻新材料技术有限公司 弹性涂料及其制备方法
CN109554101A (zh) * 2018-11-15 2019-04-02 唐山东方雨虹防水技术有限责任公司 一种聚氨酯防水涂料
CN109761834A (zh) * 2019-03-05 2019-05-17 郁维铭 一种水可分散的聚天门冬氨酸酯树脂及水性聚脲涂料的制备方法和应用
CN112980312A (zh) * 2021-03-05 2021-06-18 亚士防水科技(滁州)有限公司 双组份聚氨酯防水涂料及其制备方法
CN114350250A (zh) * 2022-02-21 2022-04-15 中南大学 一种基于刺激响应方式的快干生物基水性聚氨酯涂料及其制备方法
CN114907761A (zh) * 2022-06-24 2022-08-16 安徽尚德轨道设备制造有限公司 一种非固化丙烯酸改性聚氨酯防水涂料
CN115536984A (zh) * 2022-11-24 2022-12-30 河北坤鹏光电科技有限公司 一种硅橡胶内置胶泥冷缩套管

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
刘子康;王新锋;段文锋;: "弹性耐候丙烯酸聚氨酯涂料的研制", 新型建筑材料, no. 01, 25 January 2015 (2015-01-25), pages 39 - 42 *
周庆军: "双组份弹性聚氨酯涂料的制备与性能研究", 中国优秀硕士学位论文全文数据库工程科技Ⅰ辑, no. 12, 15 December 2015 (2015-12-15), pages 16 - 17 *

Similar Documents

Publication Publication Date Title
CN112322248B (zh) 一种复合板用pur热熔胶及其制备方法
CN111848904A (zh) 导热无卤阻燃聚氨酯弹性体及其制备方法
CN115678395B (zh) 一种高韧高强的聚脲纳米涂层
AU2021402785A1 (en) Polyurethane modified graphene microsheet and preparation method therefor
CN113429744B (zh) 一种含MOFs的环氧树脂/聚氨酯IPNs注浆材料的制备方法
CN108440739B (zh) 一种超支化抗流挂剂及在单组份聚氨酯防水涂料中的应用
CN113999611A (zh) 一种耐老化型单组分聚氨酯防水涂料
CN108384022B (zh) 一种提高非固化橡胶沥青耐高温性能超支化树脂的制备
CN116855165A (zh) 高性能聚氨酯防水涂料
CN110845938B (zh) 一种增韧改性水性环氧树脂防水涂料及其制备方法
CN108276550B (zh) 一种大豆油基聚氨酯/环氧树脂灌浆材料及其制备方法
CN111269647A (zh) 一种环氧树脂改性聚氨酯涂层剂的制备方法及其应用
CN110922884A (zh) 聚氨酯型喷涂弹性体及其制备方法
CN114539891A (zh) 一种高耐候耐腐蚀户外粉末涂料
CN110630452B (zh) 一种提高风力发电机叶片耐低温性能的保护涂层
CN110835512B (zh) 塑钢板专用pur包覆胶及其制备方法
CN108865055B (zh) 一种胶黏剂及其制备方法
CN117567932B (zh) 单组分聚氨酯防水涂料用组合物、单组分聚氨酯防水涂料及其制备和应用
CN117820956B (zh) 一种水性防水涂料及其制备方法
CN113956435B (zh) 一种聚脲交联网络弹性体的制备方法
CN115851202B (zh) 一种双组分室温固化环氧树脂粘合剂及其制备方法和应用
CN116554825B (zh) 耐候丙烯酸酯聚氨酯灌封胶及其制备方法
CN117106366B (zh) 一种单组分聚脲涂料及其制备方法和应用
CN117925077A (zh) 一种环氧树脂防水涂料及其制备方法和应用
KR100579793B1 (ko) 건축용 프라이머 조성물

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination