CN108503790A - 一种双组份聚氨酯模具胶及其制备方法 - Google Patents

一种双组份聚氨酯模具胶及其制备方法 Download PDF

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CN108503790A
CN108503790A CN201810196442.6A CN201810196442A CN108503790A CN 108503790 A CN108503790 A CN 108503790A CN 201810196442 A CN201810196442 A CN 201810196442A CN 108503790 A CN108503790 A CN 108503790A
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陈由亮
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XUCHUAN CHEMICAL (SUZHOU) CO Ltd
Asahikawa Chemical (kunshan) Co Ltd
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Abstract

本发明公开了一种双组份聚氨酯模具胶及其制备方法,所述双组份聚氨酯模具胶包括多元醇组份和聚氨酯预聚体组份,所述多元醇组份包括聚环氧丙烷醚多元醇、固化剂和催化剂,所述聚氨酯预聚体组份包括异氰酸酯、聚醚多元醇和增塑剂。所述双组份聚氨酯模具胶硬度高,硬度可调节范围广。所述双组份聚氨酯模具胶包括如下步骤:按配方称量多元醇组份和聚氨酯预聚体组份,进行混合、浇注和硫化成型,得到双组份聚氨酯模具胶。

Description

一种双组份聚氨酯模具胶及其制备方法
技术领域
本发明涉及化工产品及其制备方法领域,特别涉及一种双组份聚氨酯模具胶及其制备方法。
背景技术
自人类有文字记载以来,就开始使用模具了。经过多年的实践应用,人们得到了很多材料可以用于模具的制作,如木材,蜡质,石膏,还有塑料,橡胶等天然的或合成的高分子材料等。
聚氨酯材料是近些年才发展起来的一种高分子材料,因原材料品种多,加工方法和配方多种多样,可调整范围非常大,性能介于塑料和橡胶中间,是近几年发展最快的材料之一。
聚氨酯模具胶是属于聚氨酯弹性体系列的一种产品,其工艺性能好,可常温固化成型,脱模时间短,并可添加色料调整各种颜色,特别适用于非金属模具的制作,例如水泥制品。聚氨酯模具胶成品具有很高的强度、流动性和伸长率,强度调节范围很广,且制作工艺简单,成品使用寿命长。固化成型的模具具有良好的耐磨,不收缩,不膨胀,耐水,透明和弹性好等特点。但是市面上聚氨酯模具胶组分复杂,生产成本高,并且硬度可调节范围窄,使用范围窄。
发明内容
本发明提供了一种双组份聚氨酯模具胶,用以解决上述问题。
为了解决上述技术问题,本发明的技术方案是:
一种双组份聚氨酯模具胶,包括多元醇组份和聚氨酯预聚体组份。所述多元醇组份包括聚环氧丙烷醚多元醇、固化剂和催化剂。所述聚氨酯预聚体组份包括异氰酸酯、聚醚多元醇和增塑剂。
作为优选,所述多元醇组份中,所述聚环氧丙烷醚多元醇、固化剂和催化剂的质量百分比为:
聚环氧丙烷醚多元醇 74.9~93.9%
固化剂 6%~25%
催化剂 0.05%~0.1%。
作为优选,所述聚氨酯预聚体组份中,所述异氰酸酯、聚醚多元醇和增塑剂的质量百分比如下:
异氰酸酯 25.1%~28.4%
聚醚多元醇 48%~63.6%
增塑剂 10%~25%。
作为优选,所述聚环氧丙烷醚多元醇的数均分子量为1000~6000,官能度为2或3。
作为优选,所述固化剂采用芳香二胺类固化剂。
作为优选,所述催化剂采用有机铅、有机铋、有机锌、有机锡或有机胺中的至少一种。
作为优选,所述异氰酸酯采用甲苯二异氰酸酯、二苯基甲烷二异氰酸酯及其碳化二亚胺改性物中的至少一种。
作为优选,所述聚醚多元醇的数均分子量为1000~3000,官能度为2或3。
作为优选,所述增塑剂采用柠檬酸酯类增塑剂。
与现有技术相比,本发明具有以下优点:本发明所述双组份聚氨酯模具胶,包括多元醇组份和聚氨酯预聚体组份。所述多元醇组份包括聚环氧丙烷醚多元醇、固化剂和催化剂。所述聚氨酯预聚体组份包括异氰酸酯、聚醚多元醇和增塑剂。所述双组份聚氨酯模具胶成分简单,硬度高,硬度可调节范围广,稳定性高,使用寿命长。
本发明还提供了上述双组份聚氨酯模具胶的制备方法,包括如下步骤:
按配方称量多元醇组份和聚氨酯预聚体组份,进行混合、浇注和硫化成型,得到双组份聚氨酯模具胶。
作为优选,设置混合温度25℃~45℃。
与现有技术相比,本发明具有以下优点:本发明所述双组份聚氨酯模具胶的制备方法操作简单,安全性高。
具体实施方式
下面结合具体实施例,进一步阐述本发明。应理解这些实施例仅用于说明本发明,而不用于限制本发明的应用范围。
实施例一
一种双组份聚氨酯模具胶,包括多元醇组份和聚氨酯预聚体组份。
所述多元醇组份包括聚环氧丙烷醚多元醇、固化剂和催化剂。其中,所述聚环氧丙烷醚多元醇包括聚环氧丙烷醚二元醇和聚环氧丙烷醚三元醇,所述聚环氧丙烷醚二元醇采用PPG1000和PPG2000,PPG1000为数均分子量1000、不饱和度0.005mmol/g的聚环氧丙烷醚二元醇,PPG2000为数均分子量2000、不饱和度0.005mmol/g的聚环氧丙烷醚二元醇,所述聚环氧丙烷醚三元醇采用PPG3600,PPG3600为数均分子量6000、伯羟基含量75%,聚环氧丙烷醚三元醇;所述固化剂为3,5-二甲硫基甲苯二胺;所述催化剂为有机铋催化剂。
所述多元醇组份中,各组分含量如下:
按照配方称量各组分,设置温度100~110℃、压强-0.095MPa的条件,混合均匀并脱水至水分小于0.05%,得到所述多元醇组份。
所述聚氨酯预聚体组份包括异氰酸酯、聚醚多元醇和增塑剂。其中,所述异氰酸酯包括甲苯二异氰酸酯和二苯基甲烷二异氰酸酯,所述甲苯二异氰酸酯包括2,4-甲苯二异氰酸酯和2,6-甲苯二异氰酸酯,2,4-甲苯二异氰酸酯和2,6-甲苯二异氰酸酯的质量比为4:1,所述二苯基甲烷二异氰酸酯包括4,4-二苯基甲烷二异氰酸酯和2,4-二苯基甲烷二异氰酸酯,4,4-二苯基甲烷二异氰酸酯和2,4-二苯基甲烷二异氰酸酯的质量比为1:1;所述聚醚多元醇包括聚环氧丙烷醚二元醇和聚环氧丙烷醚三元醇,所述聚环氧丙烷醚二元醇采用PPG2000,所述聚环氧丙烷醚三元醇采用ADW-32,ADW-32为数均分子量3000、不饱和度0.005mmol/g的聚环氧丙烷醚三元醇;所述增塑剂采用柠檬酸酯类增塑剂。
所述聚氨酯预聚体组份,各组分含量如下:
按照配方称量各组分,设置温度70℃~90℃的条件,混合均匀并反应2小时,得到所述聚氨酯预聚体组份。
将所述多元醇组份和聚氨酯预聚体组份按照混合比100:70的比例混合均匀,控制混合温度25℃~45℃,然后浇注,室温或加热硫化成型,得到双组份聚氨酯模具胶。
实施例二
一种双组份聚氨酯模具胶,包括多元醇组份和聚氨酯预聚体组份。
所述多元醇组份包括聚环氧丙烷醚多元醇、固化剂和催化剂。其中,所述聚环氧丙烷醚多元醇包括聚环氧丙烷醚二元醇和聚环氧丙烷醚三元醇,所述聚环氧丙烷醚二元醇采用PPG1000和PPG4000,PPG4000为数均分子量2000、不饱和度0.005mmol/g的聚环氧丙烷醚二元醇,所述聚环氧丙烷醚三元醇采用ADW-32;所述固化剂为3,5-二甲硫基甲苯二胺;所述催化剂为有机铅催化剂。
所述多元醇组份中,各组分含量如下:
按照配方称量各组分,设置温度100~110℃、压强-0.095MPa的条件,混合均匀并脱水至水分小于0.05%,得到所述多元醇组份。
所述聚氨酯预聚体组份包括异氰酸酯、聚醚多元醇和增塑剂。其中,所述异氰酸酯包括甲苯二异氰酸酯和碳化二亚胺改性二苯基甲烷二异氰酸酯,所述甲苯二异氰酸酯包括2,4-甲苯二异氰酸酯和2,6-甲苯二异氰酸酯,2,4-甲苯二异氰酸酯和2,6-甲苯二异氰酸酯的质量比为4:1;所述聚醚多元醇包括聚环氧丙烷醚二元醇和聚环氧丙烷醚三元醇,所述聚环氧丙烷醚二元醇采用PPG1000和PPG3000,PPG3000为数均分子量3000、不饱和度0.005mmol/g的聚环氧丙烷醚二元醇,所述聚环氧丙烷醚三元醇采用ADW-32;所述增塑剂采用柠檬酸酯类增塑剂。
所述聚氨酯预聚体组份,各组分含量如下:
按照配方称量各组分,设置温度70℃~90℃的条件,混合均匀并反应2小时,得到所述聚氨酯预聚体组份。
将所述多元醇组份和聚氨酯预聚体组份按照混合比100:80的比例混合均匀,控制混合温度25℃~45℃,然后浇注,室温或加热硫化成型,得到双组份聚氨酯模具胶。
实施例三
一种双组份聚氨酯模具胶,包括多元醇组份和聚氨酯预聚体组份。
所述多元醇组份包括聚环氧丙烷醚多元醇、固化剂和催化剂。其中,所述聚环氧丙烷醚多元醇包括聚环氧丙烷醚二元醇和聚环氧丙烷醚三元醇,所述聚环氧丙烷醚二元醇采用PPG3000,所述聚环氧丙烷醚三元醇采用PP105,PP105为数均分子量5000、伯羟基含量75%的聚环氧丙烷醚三元醇;所述固化剂为3,5-二甲硫基甲苯二胺;所述催化剂为有机锡催化剂。
所述多元醇组份中,各组分含量如下:
按照配方称量各组分,设置温度100~110℃、压强-0.095MPa的条件,混合均匀并脱水至水分小于0.05%,得到所述多元醇组份。
所述聚氨酯预聚体组份包括异氰酸酯、聚醚多元醇和增塑剂。其中,所述异氰酸酯包括甲苯二异氰酸酯和二苯基甲烷二异氰酸酯,所述甲苯二异氰酸酯包括2,4-甲苯二异氰酸酯和2,6-甲苯二异氰酸酯,2,4-甲苯二异氰酸酯和2,6-甲苯二异氰酸酯的质量比为4:1,所述二苯基甲烷二异氰酸酯包括4,4-二苯基甲烷二异氰酸酯和2,4-二苯基甲烷二异氰酸酯,4,4-二苯基甲烷二异氰酸酯和2,4-二苯基甲烷二异氰酸酯的质量比为1:1;所述聚醚多元醇包括聚环氧丙烷醚二元醇和聚环氧丙烷醚三元醇,所述聚环氧丙烷醚二元醇采用PPG3000,所述聚环氧丙烷醚三元醇采用ADW-32;所述增塑剂采用柠檬酸酯类增塑剂。
所述聚氨酯预聚体组份,各组分含量如下:
按照配方称量各组分,设置温度70℃~90℃的条件,混合均匀并反应2小时,得到所述聚氨酯预聚体组份。
将所述多元醇组份和聚氨酯预聚体组份按照混合比100:100的比例混合均匀,控制混合温度25℃~45℃,然后浇注,室温或加热硫化成型,得到双组份聚氨酯模具胶。
实施例四
一种双组份聚氨酯模具胶,包括多元醇组份和聚氨酯预聚体组份。
所述多元醇组份包括聚环氧丙烷醚多元醇、固化剂和催化剂。其中,所述聚环氧丙烷醚多元醇包括聚环氧丙烷醚二元醇和聚环氧丙烷醚三元醇,所述聚环氧丙烷醚二元醇采用PPG1000,所述聚环氧丙烷醚三元醇采用PP105;所述固化剂为3,5-二甲硫基甲苯二胺;所述催化剂包括有机锌催化剂和有机胺催化剂。
所述多元醇组份中,各组分含量如下:
按照配方称量各组分,设置温度100~110℃、压强-0.095MPa的条件,混合均匀并脱水至水分小于0.05%,得到所述多元醇组份。
所述聚氨酯预聚体组份包括异氰酸酯、聚醚多元醇和增塑剂。其中,所述异氰酸酯包括甲苯二异氰酸酯和碳化二亚胺改性二苯基甲烷二异氰酸酯,所述甲苯二异氰酸酯包括2,4-甲苯二异氰酸酯和2,6-甲苯二异氰酸酯,2,4-甲苯二异氰酸酯和2,6-甲苯二异氰酸酯的质量比为4:1;所述聚醚多元醇包括聚环氧丙烷醚二元醇,所述聚环氧丙烷醚二元醇采用PPG2000;所述增塑剂采用柠檬酸酯类增塑剂。
所述聚氨酯预聚体组份,各组分含量如下:
按照配方称量各组分,设置温度70℃~90℃的条件,混合均匀并反应2小时,得到所述聚氨酯预聚体组份。
将所述多元醇组份和聚氨酯预聚体组份按照混合比100:140的比例混合均匀,控制混合温度25℃~45℃,然后浇注,室温或加热硫化成型,得到双组份聚氨酯模具胶。
将实施例中制备的双组份聚氨酯模具胶采用邵氏硬度计进行测试,结果见表1。
表1实施例一~四制备的双组份聚氨酯模具胶硬度测试结果
实施例一 实施例二 实施例三 实施例四
硬度 shoreA60 shoreA70 shoreA80 shoreA90
由表1可知,实施例一~四制备的双组份聚氨酯模具胶硬度高,且硬度调节范围广,适用范围广,并且所述双组份聚氨酯模具胶制作工艺简单,生产成本低。
本领域的技术人员可以对发明进行各种改动和变型而不脱离本发明的精神和范围。这样,倘若本发明的这些修改和变型属于本发明权利要求及其等同技术的范围之内,则本发明也意图包括这些改动和变型在内。

Claims (10)

1.一种双组份聚氨酯模具胶,包括多元醇组份和聚氨酯预聚体组份,其特征在于,所述多元醇组份包括聚环氧丙烷醚多元醇、固化剂和催化剂,所述聚氨酯预聚体组份包括异氰酸酯、聚醚多元醇和增塑剂。
2.根据权利要求1所述的双组份聚氨酯模具胶,其特征在于,所述多元醇组份中,所述聚环氧丙烷醚多元醇、固化剂和催化剂的质量百分比为:
聚环氧丙烷醚多元醇 74.9~93.9%
固化剂 6%~25%
催化剂 0.05%~0.1%。
3.根据权利要求1所述的双组份聚氨酯模具胶,其特征在于,所述聚环氧丙烷醚多元醇的数均分子量为1000~6000,官能度为2或3。
4.根据权利要求1所述的双组份聚氨酯模具胶,其特征在于,所述固化剂采用芳香二胺类固化剂。
5.根据权利要求1所述的双组份聚氨酯模具胶,其特征在于,所述催化剂采用有机铅、有机铋、有机锌、有机锡或有机胺中的至少一种。
6.根据权利要求1所述的双组份聚氨酯模具胶,其特征在于,所述聚氨酯预聚体组份中,所述异氰酸酯、聚醚多元醇和增塑剂的质量百分比如下:
异氰酸酯 25.1%~28.4%
聚醚多元醇 48%~63.6%
增塑剂 10%~25%。
7.根据权利要求1所述的双组份聚氨酯模具胶,其特征在于,所述异氰酸酯采用甲苯二异氰酸酯、二苯基甲烷二异氰酸酯及其碳化二亚胺改性物中的至少一种。
8.根据权利要求1所述的双组份聚氨酯模具胶,其特征在于,所述聚醚多元醇的数均分子量为1000~3000,官能度为2或3。
9.根据权利要求1所述的双组份聚氨酯模具胶,其特征在于,所述增塑剂采用柠檬酸酯类增塑剂。
10.一种如权利要求1~9所述的双组份聚氨酯模具胶的制备方法,其特征在于,包括如下步骤:按配方称量多元醇组份和聚氨酯预聚体组份,进行混合、浇注和硫化成型,得到双组份聚氨酯模具胶。
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