CN108949090A - 一种无溶剂双组份聚氨酯密封胶及其制备方法 - Google Patents

一种无溶剂双组份聚氨酯密封胶及其制备方法 Download PDF

Info

Publication number
CN108949090A
CN108949090A CN201810805906.9A CN201810805906A CN108949090A CN 108949090 A CN108949090 A CN 108949090A CN 201810805906 A CN201810805906 A CN 201810805906A CN 108949090 A CN108949090 A CN 108949090A
Authority
CN
China
Prior art keywords
parts
component
solvent
polyurethane sealant
diisocyanate
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.)
Granted
Application number
CN201810805906.9A
Other languages
English (en)
Other versions
CN108949090B (zh
Inventor
刘明星
孙学武
周静静
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.)
Anhui Craftsman Lian New Mstar Technology Ltd
Original Assignee
Anhui Craftsman Lian New Mstar Technology 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 Anhui Craftsman Lian New Mstar Technology Ltd filed Critical Anhui Craftsman Lian New Mstar Technology Ltd
Priority to CN201810805906.9A priority Critical patent/CN108949090B/zh
Publication of CN108949090A publication Critical patent/CN108949090A/zh
Application granted granted Critical
Publication of CN108949090B publication Critical patent/CN108949090B/zh
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J175/00Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
    • C09J175/04Polyurethanes
    • C09J175/08Polyurethanes 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
    • C08G18/30Low-molecular-weight compounds
    • C08G18/32Polyhydroxy compounds; Polyamines; Hydroxyamines
    • C08G18/3203Polyhydroxy compounds
    • C08G18/3206Polyhydroxy compounds aliphatic
    • 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
    • C08G18/30Low-molecular-weight compounds
    • C08G18/34Carboxylic acids; Esters thereof with monohydroxyl compounds
    • C08G18/348Hydroxycarboxylic acids
    • 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
    • C08G18/4825Polyethers containing two hydroxy groups
    • 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
    • C08G18/4829Polyethers containing at least three hydroxy groups
    • 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
    • C08G18/4854Polyethers containing oxyalkylene groups having four carbon atoms in the alkylene group
    • 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
    • C08G18/50Polyethers having heteroatoms other than oxygen
    • C08G18/5021Polyethers having heteroatoms other than oxygen having nitrogen
    • C08G18/5024Polyethers having heteroatoms other than oxygen having nitrogen containing primary and/or secondary amino groups
    • 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
    • C08G18/65Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
    • C08G18/66Compounds of groups C08G18/42, C08G18/48, or C08G18/52
    • C08G18/6666Compounds of group C08G18/48 or C08G18/52
    • C08G18/667Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38
    • C08G18/6674Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3203
    • 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
    • C08G18/65Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
    • C08G18/66Compounds of groups C08G18/42, C08G18/48, or C08G18/52
    • C08G18/6666Compounds of group C08G18/48 or C08G18/52
    • C08G18/667Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38
    • C08G18/6674Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3203
    • C08G18/6677Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3203 having at least three hydroxy groups
    • 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
    • C08G18/65Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
    • C08G18/66Compounds of groups C08G18/42, C08G18/48, or C08G18/52
    • C08G18/6666Compounds of group C08G18/48 or C08G18/52
    • C08G18/6692Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/34

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Sealing Material Composition (AREA)

Abstract

本发明公开了一种无溶剂双组份聚氨酯密封胶及其制备方法,涉及胶黏剂产品制备技术领域,由如下重量份数的原料制成:甲组份:二异氰酸酯30‑40份、聚醚多元醇40‑60份、扩链剂2‑4份、催化剂1‑2份;乙组份:填充剂300‑550份、端氨基聚醚50‑100份、增塑剂100‑150份、聚丙烯酸酯多元醇50‑90份、消泡剂1‑3份、抗氧化剂1‑3份、紫外吸收剂1‑3份、触变剂2‑4份。本发明合成的聚氨酯密封胶材料为无溶剂型,不添加有机溶剂,环保性强;表干时间短,模量高,粘结强度高,可广泛应用于玻璃、钢板、建筑粘结等领域。

Description

一种无溶剂双组份聚氨酯密封胶及其制备方法
技术领域:
本发明涉及胶黏剂产品制备技术领域,具体涉及一种无溶剂双组份聚氨酯密封胶及其制备方法。
背景技术:
密封胶是用于填充孔洞、接缝等间隙的膏状材料,它固化后将基材粘接成一个整体,具有防水、防尘、防雾等功能,广泛应用于建筑、汽车、机械、电子等领域。
聚氨酯密封胶是三大弹性密封胶(有机硅、聚硫、聚氨酯)之一,具有优良的弹性、耐低温性、耐磨性和对基材良好的粘附性。聚氨酯密封胶由于含有极性基团、柔性链段和刚性链段共聚,与含有活泼氢的材料和表面光洁的材料都有优良的化学粘合力,有良好的粘性性能、机械性能以及耐化学腐蚀、耐热、耐低温等性能,并且施工时无收缩,断裂伸长率高。聚氨酯密封胶因其可调性范围广,且粘结力强作为粘结和弹性密封材料已得到广泛的应用,使用寿命可达15-20年,价格相对较低。
聚氨酯密封胶按照组份可分为单组份和双组份,其中单组份湿固化型聚氨酯密封胶由于使用方便,主要应用于汽车内饰、车窗玻璃、室内装修等领域;而双组份密封胶具有固化迅速、硬度可调节、模量高及保质期长等特点,现场使用时根据需要现场调配,主要应用于汽车、建筑等领域。
传统的双组份聚氨酯密封胶一般都添加有机溶剂,不符合环保的发展要求,无溶剂型双组份聚氨酯密封胶成为行业的研究热点,并将逐步取代传统产品。
专利CN105238330B公开了一种无溶剂双组份聚氨酯密封胶,包含A组分和B组分,A组分由聚醚多元醇DDL-1000D、聚醚多元醇DMN-1000、MDI组成,B组分由扩链剂、交联剂、增塑剂、催化剂、触变剂、发泡抑制剂组成。首先,A组分通过聚醚多元醇与MDI反应生成聚氨酯预聚体,再通过与B组分的混合使聚氨酯预聚体结构上多余的-NCO与B组分中聚醚多元醇的-OH继续反应,因此所制密封胶的主要成分仍是聚氨酯,而并未在聚氨酯结构上引入其他能够改善密封胶使用性能的功能团;其次,B组分中没有添加填料,A组分与B组分的混合质量比为2:1,这样会直接导致其加工成本升高。
发明内容:
本发明所要解决的技术问题在于提供一种环保性强、固化速度快、力学性能优异的无溶剂双组份聚氨酯密封胶及其制备方法。
本发明所要解决的技术问题采用以下的技术方案来实现:
一种无溶剂双组份聚氨酯密封胶,由如下重量份数的原料制成:
甲组份:二异氰酸酯30-40份、聚醚多元醇40-60份、扩链剂2-4份、催化剂1-2份;
乙组份:填充剂300-550份、端氨基聚醚50-100份、增塑剂100-150份、聚丙烯酸酯多元醇50-90份、消泡剂1-3份、抗氧化剂1-3份、紫外吸收剂1-3份、触变剂2-4份。
所述二异氰酸酯选自甲苯二异氰酸酯TDI、异佛尔酮二异氰酸酯IPDI、二苯基甲烷二异氰酸酯MDI、1,6-己二异氰酸酯HDI、苯二亚甲基二异氰酸酯XDI、萘-1,5-二异氰酸酯NDI、多亚甲基多苯基异氰酸酯PAPI中的一种或两种。
所述聚醚多元醇选自聚四氢呋喃二元醇PTMG、聚氧化丙烯多元醇PPG、端氨基聚醚类中的一种或两种,官能度为2~4,数均分子量为1000~5000。
所述扩链剂选自二羟甲基丙酸、丁二醇、新戊二醇、三羟甲基丙烷中的一种。
所述催化剂选自二月桂酸二丁基锡、异辛酸铋、新癸酸铋、环烷酸铋、月桂酸铋中的一种。
所述端氨基聚醚选自共聚醚二胺D-2000、D-4000、ED-600、ED-900中的一种或两种。
所述填充剂选自滑石粉、碳酸钙、高岭土、白炭黑中的一种或两种。
所述增塑剂选自邻苯二甲酸酯、脂肪族二酸酯、氯化石蜡中的一种或两种。
所述聚丙烯酸酯多元醇的羟基含量为2%~4%。
所述消泡剂为聚醚改性硅氧烷共聚合物。
所述抗氧剂选自1010、1035、1076 8中的一种。
所述紫外吸收剂选自UV-1130、UV-234中的一种。
所述触变剂选自气相二氧化硅、有机膨润土中的一种。
上述无溶剂双组份聚氨酯密封胶的制备方法包括以下步骤:
(1)甲组份的制备:向三口烧瓶中加入聚醚多元醇,升温至100~110℃脱水1~3h,再降温至70~80℃加入二异氰酸酯,氮气保护下加入催化剂,保温反应2h,然后加入扩链剂,继续保温反应2h,生成稳定的预聚体后降至常温,密封保存,即得甲组份;
(2)乙组份的制备:向三口烧瓶中先加入聚丙烯酸酯多元醇、端氨基聚醚、增塑剂和消泡剂,搅拌均匀后再加入填充剂、抗氧化剂和紫外吸收剂,再次搅拌均匀,最后加入触变剂,搅拌均匀后密封保存,即得乙组份;
(3)施工使用:按甲组份:乙组份=1:4~1:6比例混合均匀,再加入总重0.5%~1%的催化剂,快速搅拌均匀后使用。
本发明的有益效果是:
(1)本发明先分别合成甲组份和乙组份,甲组份为-NCO封端的聚氨酯树脂预聚物,乙组份为含-NH2、-OH以及各种填充剂和助剂的混合物,使用时将甲组份与乙组份按比例混合均匀并加入催化剂后即可使用,-NCO与-NH2、-OH反应,粘合速度快,强度高、耐候性强。
(2)本发明合成的聚氨酯密封胶材料为无溶剂型,不添加有机溶剂,环保性强;表干时间短,模量高,粘结强度高,可广泛应用于玻璃、钢板、建筑粘结等领域。
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。
实施例1
按如下配比进行备料:
(1)甲组份的制备:向三口烧瓶中加入聚四氢呋喃二元醇和聚氧化丙烯二元醇2000,升温至100~110℃脱水2h,再降温至70~80℃加入二异氰酸酯TDI-100,氮气保护下加入催化剂二月桂酸二丁基锡,保温反应2h,然后加入扩链剂新戊二醇,继续保温反应2h,生成稳定的预聚体后降至常温,密封保存,即得甲组份;
(2)乙组份的制备:向三口烧瓶中先加入聚丙烯酸酯多元醇、共聚醚二胺D-2000、增塑剂邻苯二甲酸酯和消泡剂聚醚改性硅氧烷共聚合物,搅拌均匀后再加入填充剂滑石粉与高岭土、抗氧化剂1010和紫外吸收剂UV-1130,再次搅拌均匀,最后加入触变剂二氧化硅,搅拌均匀后密封保存,即得乙组份;
(3)施工使用:按甲组份:乙组份=1:5比例混合均匀,再加入总重0.5%的催化剂二月桂酸二丁基锡,快速搅拌均匀后使用。
实施例2
按如下配比进行备料:
(1)甲组份的制备:向三口烧瓶中加入聚四氢呋喃二元醇和聚氧化丙烯三元醇3000,升温至100~110℃脱水2h,再降温至70~80℃加入二异氰酸酯MDI,氮气保护下加入催化剂二月桂酸二丁基锡,保温反应2h,然后加入扩链剂二羟甲基丙酸,继续保温反应2h,生成稳定的预聚体后降至常温,密封保存,即得甲组份;
(2)乙组份的制备:向三口烧瓶中先加入聚丙烯酸酯多元醇、共聚醚二胺D-2000、增塑剂邻苯二甲酸酯和消泡剂聚醚改性硅氧烷共聚合物,搅拌均匀后再加入填充剂碳酸钙与高岭土、抗氧化剂1010和紫外吸收剂UV-234,再次搅拌均匀,最后加入触变剂二氧化硅,搅拌均匀后密封保存,即得乙组份;
(3)施工使用:按甲组份:乙组份=1:4比例混合均匀,再加入总重0.5%的催化剂二月桂酸二丁基锡,快速搅拌均匀后使用。
实施例3
按如下配比进行备料:
(1)甲组份的制备:向三口烧瓶中加入聚氧化丙烯二元醇4000和聚氧化丙烯二元醇2000,升温至100~110℃脱水2h,再降温至70~80℃加入二异氰酸酯MDI,氮气保护下加入催化剂异辛酸铋,保温反应2h,然后加入扩链剂丁二醇,继续保温反应2h,生成稳定的预聚体后降至常温,密封保存,即得甲组份;
(2)乙组份的制备:向三口烧瓶中先加入聚丙烯酸酯多元醇、共聚醚二胺ED-600、增塑剂脂肪族二酸酯和消泡剂聚醚改性硅氧烷共聚合物,搅拌均匀后再加入填充剂碳酸钙与滑石粉、抗氧化剂1035和紫外吸收剂UV-1130,再次搅拌均匀,最后加入触变剂有机膨润土,搅拌均匀后密封保存,即得乙组份;
(3)施工使用:按甲组份:乙组份=1:5比例混合均匀,再加入总重0.5%的催化剂异辛酸铋,快速搅拌均匀后使用。
实施例4
按如下配比进行备料:
(1)甲组份的制备:向三口烧瓶中加入聚四氢呋喃二元醇和聚氧化丙烯二元醇4000,升温至100~110℃脱水2h,再降温至70~80℃加入二异氰酸酯IPDI,氮气保护下加入催化剂异辛酸铋,保温反应2h,然后加入扩链剂三羟甲基丙烷,继续保温反应2h,生成稳定的预聚体后降至常温,密封保存,即得甲组份;
(2)乙组份的制备:向三口烧瓶中先加入聚丙烯酸酯多元醇、共聚醚二胺D-4000、增塑剂邻苯二甲酸酯和消泡剂聚醚改性硅氧烷共聚合物,搅拌均匀后再加入填充剂碳酸钙与白炭黑、抗氧化剂1010和紫外吸收剂UV-1130,再次搅拌均匀,最后加入触变剂二氧化硅,搅拌均匀后密封保存,即得乙组份;
(3)施工使用:按甲组份:乙组份=1:5比例混合均匀,再加入总重0.5%的催化剂异辛酸铋,快速搅拌均匀后使用。
对照例1
以实施例1为基础,设置在乙组份制备时不添加共聚醚二胺D-2000的对照例1。
按如下配比进行备料:
(1)甲组份的制备:向三口烧瓶中加入聚四氢呋喃二元醇和聚氧化丙烯二元醇2000,升温至100~110℃脱水2h,再降温至70~80℃加入二异氰酸酯TDI-100,氮气保护下加入催化剂二月桂酸二丁基锡,保温反应2h,然后加入扩链剂新戊二醇,继续保温反应2h,生成稳定的预聚体后降至常温,密封保存,即得甲组份;
(2)乙组份的制备:向三口烧瓶中先加入聚丙烯酸酯多元醇、增塑剂邻苯二甲酸酯和消泡剂聚醚改性硅氧烷共聚合物,搅拌均匀后再加入填充剂滑石粉与高岭土、抗氧化剂1010和紫外吸收剂UV-1130,再次搅拌均匀,最后加入触变剂二氧化硅,搅拌均匀后密封保存,即得乙组份;
(3)施工使用:按甲组份:乙组份=1:5比例混合均匀,再加入总重0.5%的催化剂二月桂酸二丁基锡,快速搅拌均匀后使用。
对照例2
以实施例1为基础,设置在乙组份制备时不添加聚丙烯酸酯多元醇的对照例2。
按如下配比进行备料:
(1)甲组份的制备:向三口烧瓶中加入聚四氢呋喃二元醇和聚氧化丙烯二元醇2000,升温至100~110℃脱水2h,再降温至70~80℃加入二异氰酸酯TDI-100,氮气保护下加入催化剂二月桂酸二丁基锡,保温反应2h,然后加入扩链剂新戊二醇,继续保温反应2h,生成稳定的预聚体后降至常温,密封保存,即得甲组份;
(2)乙组份的制备:向三口烧瓶中先加入共聚醚二胺D-2000、增塑剂邻苯二甲酸酯和消泡剂聚醚改性硅氧烷共聚合物,搅拌均匀后再加入填充剂滑石粉与高岭土、抗氧化剂1010和紫外吸收剂UV-1130,再次搅拌均匀,最后加入触变剂二氧化硅,搅拌均匀后密封保存,即得乙组份;
(3)施工使用:按甲组份:乙组份=1:5比例混合均匀,再加入总重0.5%的催化剂二月桂酸二丁基锡,快速搅拌均匀后使用。
实施例5
分别利用实施例1-4、对照例1-2制备聚氨酯密封胶,对所制聚氨酯密封胶的使用性能进行测试,测试结果如表1所示,并与法国Bostik生产的Simson ISR70-08、专利CN105238330B实施例1所制聚氨酯密封胶进行性能比较。
测试标准:拉伸强度GB/T 528-2009;扯断伸长率GB/T 528-2009;剪切强度GB/T7124-2008。
挤出适量聚氨酯密封胶在聚四氟乙烯板上,用抹灰刀刮成厚度2mm的胶层,勿使胶内存有气泡,在标准环境下放置7天后,测试耐候性能。
耐候性能:将固化7天后的胶片放进紫外线老化试验箱中,每隔一段时间观察外观,用不干胶粘胶片表面,测试拉伸强度、扯断伸长率和剪切强度。
表1本发明实施例所制聚氨酯密封胶的使用性能
由表1可知,本发明实施例1-4所制双组份聚氨酯密封胶的拉伸强度、扯断伸长率、剪切强度和耐候性均强于法国Bostik生产的Simson ISR70-08和专利CN 105238330B实施例1所制聚氨酯密封胶;而在乙组份制备时不添加共聚醚二胺D-2000的对照例1以及在乙组份制备时不添加聚丙烯酸酯多元醇的对照例2所制双组份聚氨酯密封胶的拉伸强度、扯断伸长率、剪切强度和耐候性相对于实施例1均出现不同程度的降低。
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 (10)

1.一种无溶剂双组份聚氨酯密封胶,其特征在于,由如下重量份数的原料制成:
甲组份:二异氰酸酯30-40份、聚醚多元醇40-60份、扩链剂2-4份、催化剂1-2份;
乙组份:填充剂300-550份、端氨基聚醚50-100份、增塑剂100-150份、聚丙烯酸酯多元醇50-90份、消泡剂1-3份、抗氧化剂1-3份、紫外吸收剂1-3份、触变剂2-4份。
2.根据权利要求1所述的无溶剂双组份聚氨酯密封胶,其特征在于,其制备方法包括以下步骤:
(1)甲组份的制备:向三口烧瓶中加入聚醚多元醇,升温至100~110℃脱水1~3h,再降温至70~80℃加入二异氰酸酯,氮气保护下加入催化剂,保温反应2h,然后加入扩链剂,继续保温反应2h,生成稳定的预聚体后降至常温,密封保存,即得甲组份;
(2)乙组份的制备:向三口烧瓶中先加入聚丙烯酸酯多元醇、端氨基聚醚、增塑剂和消泡剂,搅拌均匀后再加入填充剂、抗氧化剂和紫外吸收剂,再次搅拌均匀,最后加入触变剂,搅拌均匀后密封保存,即得乙组份;
(3)施工使用:按甲组份:乙组份=1:4~1:6比例混合均匀,再加入总重0.5%~1%的催化剂,快速搅拌均匀后使用。
3.根据权利要求1或2所述的无溶剂双组份聚氨酯密封胶,其特征在于:所述二异氰酸酯选自甲苯二异氰酸酯TDI、异佛尔酮二异氰酸酯IPDI、二苯基甲烷二异氰酸酯MDI、1,6-己二异氰酸酯HDI、苯二亚甲基二异氰酸酯XDI、萘-1,5-二异氰酸酯NDI、多亚甲基多苯基异氰酸酯PAPI中的一种或两种。
4.根据权利要求1或2所述的无溶剂双组份聚氨酯密封胶,其特征在于:所述聚醚多元醇选自聚四氢呋喃二元醇PTMG、聚氧化丙烯多元醇PPG、端氨基聚醚类中的一种或两种,官能度为2~4,数均分子量为1000~5000。
5.根据权利要求1或2所述的无溶剂双组份聚氨酯密封胶,其特征在于:所述扩链剂选自二羟甲基丙酸、丁二醇、新戊二醇、三羟甲基丙烷中的一种;催化剂选自二月桂酸二丁基锡、异辛酸铋、新癸酸铋、环烷酸铋、月桂酸铋中的一种。
6.根据权利要求1或2所述的无溶剂双组份聚氨酯密封胶,其特征在于:所述端氨基聚醚选自共聚醚二胺D-2000、D-4000、ED-600、ED-900中的一种或两种。
7.根据权利要求1或2所述的无溶剂双组份聚氨酯密封胶,其特征在于:所述填充剂选自滑石粉、碳酸钙、高岭土、白炭黑中的一种或两种;增塑剂选自邻苯二甲酸酯、脂肪族二酸酯、氯化石蜡中的一种或两种。
8.根据权利要求1或2所述的无溶剂双组份聚氨酯密封胶,其特征在于:所述聚丙烯酸酯多元醇的羟基含量为2%~4%。
9.根据权利要求1或2所述的无溶剂双组份聚氨酯密封胶,其特征在于:所述消泡剂为聚醚改性硅氧烷共聚合物。
10.根据权利要求1或2所述的无溶剂双组份聚氨酯密封胶,其特征在于:所述抗氧剂选自1010、1035、1076 8中的一种;紫外吸收剂选自UV-1130、UV-234中的一种;触变剂选自气相二氧化硅、有机膨润土中的一种。
CN201810805906.9A 2018-07-20 2018-07-20 一种无溶剂双组份聚氨酯密封胶及其制备方法 Active CN108949090B (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810805906.9A CN108949090B (zh) 2018-07-20 2018-07-20 一种无溶剂双组份聚氨酯密封胶及其制备方法

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810805906.9A CN108949090B (zh) 2018-07-20 2018-07-20 一种无溶剂双组份聚氨酯密封胶及其制备方法

Publications (2)

Publication Number Publication Date
CN108949090A true CN108949090A (zh) 2018-12-07
CN108949090B CN108949090B (zh) 2020-12-08

Family

ID=64497934

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810805906.9A Active CN108949090B (zh) 2018-07-20 2018-07-20 一种无溶剂双组份聚氨酯密封胶及其制备方法

Country Status (1)

Country Link
CN (1) CN108949090B (zh)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109749043A (zh) * 2018-12-29 2019-05-14 浙江华峰合成树脂有限公司 高剥离革用无溶剂聚氨酯树脂及其制备方法和应用
CN111876097A (zh) * 2020-07-03 2020-11-03 江门市长河化工实业集团有限公司 一种预制型的聚氨酯运动地胶及其制备方法
CN111892901A (zh) * 2019-05-05 2020-11-06 郑州大学 一种中空玻璃用快固化双组份聚氨酯密封胶及其制备方法
WO2021109025A1 (zh) * 2019-12-04 2021-06-10 杭州之江新材料有限公司 双组分聚氨酯粘合剂组合物及其粘合方法

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20150322314A1 (en) * 2013-01-25 2015-11-12 Henkel Ag & Co. Kgaa Moisture-Curing Polyurethane Composition Comprising Sustainably Produced Raw Materials
CN105238330A (zh) * 2015-11-13 2016-01-13 淄博正大聚氨酯有限公司 聚氨酯密封胶及其制备方法
CN107652934A (zh) * 2017-09-30 2018-02-02 温州生物材料与工程研究所 一种室温超快速固化双组份无溶剂聚氨酯结构胶及其制备和使用方法
CN107880234A (zh) * 2017-11-27 2018-04-06 烟台德邦科技有限公司 一种耐高温的聚氨酯热熔胶的制备方法
CN108192494A (zh) * 2018-01-10 2018-06-22 安徽匠星联创新材料科技有限公司 一种透气自结纹型运动场地材料及制备方法

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20150322314A1 (en) * 2013-01-25 2015-11-12 Henkel Ag & Co. Kgaa Moisture-Curing Polyurethane Composition Comprising Sustainably Produced Raw Materials
CN105238330A (zh) * 2015-11-13 2016-01-13 淄博正大聚氨酯有限公司 聚氨酯密封胶及其制备方法
CN107652934A (zh) * 2017-09-30 2018-02-02 温州生物材料与工程研究所 一种室温超快速固化双组份无溶剂聚氨酯结构胶及其制备和使用方法
CN107880234A (zh) * 2017-11-27 2018-04-06 烟台德邦科技有限公司 一种耐高温的聚氨酯热熔胶的制备方法
CN108192494A (zh) * 2018-01-10 2018-06-22 安徽匠星联创新材料科技有限公司 一种透气自结纹型运动场地材料及制备方法

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109749043A (zh) * 2018-12-29 2019-05-14 浙江华峰合成树脂有限公司 高剥离革用无溶剂聚氨酯树脂及其制备方法和应用
CN109749043B (zh) * 2018-12-29 2021-07-16 浙江华峰合成树脂有限公司 高剥离革用无溶剂聚氨酯树脂及其制备方法和应用
CN111892901A (zh) * 2019-05-05 2020-11-06 郑州大学 一种中空玻璃用快固化双组份聚氨酯密封胶及其制备方法
WO2021109025A1 (zh) * 2019-12-04 2021-06-10 杭州之江新材料有限公司 双组分聚氨酯粘合剂组合物及其粘合方法
EP3858938A4 (en) * 2019-12-04 2021-08-04 Hangzhou Zhijiang New Material Co., Ltd. TWO-COMPONENT POLYURETHANE ADHESIVE COMPOSITION AND CONNECTING METHOD FOR IT
CN111876097A (zh) * 2020-07-03 2020-11-03 江门市长河化工实业集团有限公司 一种预制型的聚氨酯运动地胶及其制备方法

Also Published As

Publication number Publication date
CN108949090B (zh) 2020-12-08

Similar Documents

Publication Publication Date Title
CN108949090A (zh) 一种无溶剂双组份聚氨酯密封胶及其制备方法
TWI359158B (en) Prepolymer compositions and sealants made therefro
AU1323199A (en) Process for producing prepolymers which cure to improved sealants, and products formed thereby
KR102352078B1 (ko) 폴리우레아 도료 조성물
CN109207111A (zh) 一种单组份聚氨酯密封胶及其制备方法
CN104356340A (zh) 一种聚氨酯预聚体及包含其的双组分聚氨酯嵌缝材料、制备方法和应用
JPH07113073A (ja) 艶消しシーリング組成物
CN109777338A (zh) 高强度高断裂伸长率单组分聚氨酯胶粘剂及制备方法
CN104194603A (zh) 聚碳酸酯型聚氨酯防水涂料
JP2007508417A5 (zh)
CN111471155A (zh) 一种硅烷封端改性聚氨酯树脂、高强度低模量改性聚氨酯密封胶及其制备方法
CN100528920C (zh) 一种高固体分单组分聚氨酯弹性体的制备方法及其应用
CN101245182B (zh) 密封胶用耐高温耐水聚氨酯组合物及其制备方法
KR20110131717A (ko) 친환경 탄성접착제용 습기경화형 폴리우레탄 수지 조성물 및 그 제조방법
JP2009132832A (ja) 一液型ポリウレタン系硬化性組成物およびこれを用いた接着剤
JP4800653B2 (ja) 建築ワーキングジョイント用1成分形ウレタン系シーリング材組成物及びその施工方法
CN115386287A (zh) 一种耐候高强度弹性涂料及其制备方法和应用
CN113980563B (zh) 用于制备单组份半聚脲防水涂料组合物的方法、单组份半聚脲防水涂料组合物
CN105199653A (zh) 一种高强度低粘度硅烷改性聚氨酯树脂
CN113527629B (zh) 一种高耐候高性能建筑外墙用改性聚醚树脂及密封胶
CN102203207B (zh) 指触干燥的可湿气固化的组合物及由其制备的产品
CN115785850B (zh) 一种增粘促进剂及其制备方法和应用以及耐水粘接单组分聚氨酯密封胶及其制备方法和应用
CN115160914B (zh) 一种专用于背水面防水修缮工程的单组分聚氨酯防水涂料
JP5776387B2 (ja) 建築用シーリング材または塗膜防水材の下地処理用1液湿気硬化型プライマー
KR20180016516A (ko) 접착제 조성물 및 그 제조 방법

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
GR01 Patent grant
GR01 Patent grant
PE01 Entry into force of the registration of the contract for pledge of patent right

Denomination of invention: A solvent-free two component polyurethane sealant and its preparation method

Effective date of registration: 20230630

Granted publication date: 20201208

Pledgee: Lu'an Yeji Sub branch of Agricultural Bank of China Co.,Ltd.

Pledgor: ANHUI JIANGXING LIANCHUANG NEW MATERIALS TECHNOLOGY CO.,LTD.

Registration number: Y2023980046766

PE01 Entry into force of the registration of the contract for pledge of patent right