CN104356908A - 一种改进型涂料合成方法 - Google Patents
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Abstract
本发明涉及一种改进型涂料合成方法,包括如下步骤:在干燥氮气的保护下,将KH550和环氧树脂按计量加入四口瓶烧瓶中,混合均匀后常温反应,得到组分A;在干燥氮气的保护下,将真空脱水后的聚醚、组分A与IPDI按计量加入三口烧瓶中;再加入计量好的一缩二乙二醇、TMP作交联剂、DM-PA、丙酮和几滴催化剂反应后出料;将预聚体用三乙胺中和加水进行高速乳化,然后加入乙二胺稀释液反应,得到水性聚氨酯乳液;将乳液减压蒸馏脱出丙酮即得环氧树脂用KH 550开环改性水性聚氨酯涂料。本发明方法简单、成本低廉,重复性好,获得的环氧树脂用KH550开环改性水性聚氨酯涂料性能稳定、分散性好。
Description
技术领域
本发明涉及有机涂料合成技术领域,尤其涉及一种改进型涂料合成方法。
背景技术
随着环保法规的逐渐加强,低VOC(甚至零VOC)、无毒、无污染的新材料水性聚氨酯越来越受人们的重视。水性聚氨酯广泛应用于粘接剂、涂料、纺织、印染、制革等工业领域。但未经改性的水性聚氨酯乳液存在耐水性差、机械强度不够等缺点,较大程度上限制了其应用领域。有机硅化合物是一种特殊高分子化合物,它们兼有无机化合物和有机化合物的特性,具有耐低温、耐老化、憎水、耐有机溶剂,耐辐射等许多优异性能,而且有机硅化合物还能赋予涂层杰出柔软性和爽滑性,有丝绸手感或蜡感。环氧树酯(EP)具有许多优良的性能、机械强度高,粘附力强,成型收缩率低,化学性能稳定。
目前,含有氨基的有机硅氧烷改性水性聚氨酯主要有两种方法,一种是在合成过程中将氨基硅油引入聚氨酯链段中,但由于氨基硅油突出的反应活性以及与聚氨酯溶解度的差异,所以聚合反应都需要在溶剂的存在下进行,存在环境污染问题,使它们的应用受到限制;另一种是在预聚体乳化的过程中扩链引入氨基硅油。氨基硅油改性的水性聚氨酯能形成稳定的乳液,有利于实际的应用,所得涂膜耐水性、表面疏水性等性能都有明显提高,而材料的力学性能并没有太大改变。
发明内容
本发明所要解决的技术问题是提供一种方法简单、成本低廉,重复性好,获得的环氧树脂用KH550开环改性水性聚氨酯涂料性能稳定、分散性好的合成方法。
本发明解决上述技术问题的技术方案如下:一种改进型涂料合成方法,包括如下步骤:
在干燥氮气的保护下,将KH550和环氧树脂按计量加入四口瓶烧瓶中,混合均匀后常温反应,得到组分A;
在干燥氮气的保护下,将真空脱水后的聚醚、组分A与IPDI按计量加入三口烧瓶中;
再加入计量好的一缩二乙二醇、TMP作交联剂、DM-PA、丙酮和几滴催化剂反应后出料;
将预聚体用三乙胺中和加水进行高速乳化,然后加入乙二胺稀释液反应,得到水性聚氨酯乳液;
将乳液减压蒸馏脱出丙酮即得环氧树脂用KH550开环改性水性聚氨酯涂料。
在上述技术方案的基础上,本发明还可以做如下改进。
进一步,所述在干燥氮气的保护下,将KH550和环氧树脂按计量加入四口瓶烧瓶中,混合均匀后常温反应,得到组分A步骤的具体实现如下:
在干燥氮气的保护下,将KH550和环氧树脂按计量加入四口瓶烧瓶中,混合均匀后常温反应1~5h,得到组分A。
进一步,所述在干燥氮气的保护下,将真空脱水后的聚醚、组分A与IPDI按计量加入三口烧瓶中步骤的具体实现如下:
在干燥氮气的保护下,将真空脱水后的聚醚、组分A与IPDI按计量加入三口烧瓶中,升温至85~90℃,反应1~2h。
进一步,所述再加入计量好的一缩二乙二醇、TMP作交联剂、DM-PA、丙酮和几滴催化剂反应后出料步骤的具体实现如下:
再加入计量好的一缩二乙二醇、TMP作交联剂、DM-PA、丙酮和几滴催化剂,在60~70℃条件下反应1~6h后,冷却到40~10℃出料。
本发明的有益效果是:方法简单、成本低廉,重复性好,获得的环氧树脂用KH550开环改性水性聚氨酯涂料性能稳定、分散性好。
具体实施方式
以下结合实例对本发明的原理和特征进行描述,所举实例只用于解释本发明,并非用于限定本发明的范围。
一种改进型涂料合成方法,包括如下步骤:
在干燥氮气的保护下,将KH550和环氧树脂按计量加入四口瓶烧瓶中,混合均匀后常温反应,得到组分A;
在干燥氮气的保护下,将真空脱水后的聚醚、组分A与IPDI按计量加入三口烧瓶中;
再加入计量好的一缩二乙二醇、TMP作交联剂、DM-PA、丙酮和几滴催化剂反应后出料;
将预聚体用三乙胺中和加水进行高速乳化,然后加入乙二胺稀释液反应,得到水性聚氨酯乳液;
将乳液减压蒸馏脱出丙酮即得环氧树脂用KH550开环改性水性聚氨酯涂料。
实施例1:
在干燥氮气的保护下,将KH550和环氧树脂按计量加入四口瓶烧瓶中,混合均匀后常温反应1h,得到组分A;在干燥氮气的保护下,将真空脱水后的聚醚、组分A与IPDI按计量加入三口烧瓶中,升温至85℃,反应1h;再加入计量好的一缩二乙二醇、TMP作交联剂、DM-PA、丙酮和几滴催化剂,在60℃条件下反应1h后,冷却到40℃出料;将预聚体用三乙胺中和加水进行高速乳化,然后加入乙二胺稀释液反应,得到水性聚氨酯乳液;将乳液减压蒸馏脱出丙酮即得环氧树脂用KH550开环改性水性聚氨酯涂料。
实施例2:
在干燥氮气的保护下,将KH550和环氧树脂按计量加入四口瓶烧瓶中,混合均匀后常温反应3h,得到组分A;在干燥氮气的保护下,将真空脱水后的聚醚、组分A与IPDI按计量加入三口烧瓶中,升温至88℃,反应1.5h;再加入计量好的一缩二乙二醇、TMP作交联剂、DM-PA、丙酮和几滴催化剂,在65℃条件下反应3h后,冷却到20℃出料;将预聚体用三乙胺中和加水进行高速乳化,然后加入乙二胺稀释液反应,得到水性聚氨酯乳液;将乳液减压蒸馏脱出丙酮即得环氧树脂用KH550开环改性水性聚氨酯涂料。
实施例3:
在干燥氮气的保护下,将KH550和环氧树脂按计量加入四口瓶烧瓶中,混合均匀后常温反应5h,得到组分A;在干燥氮气的保护下,将真空脱水后的聚醚、组分A与IPDI按计量加入三口烧瓶中,升温至90℃,反应2h;再加入计量好的一缩二乙二醇、TMP作交联剂、DM-PA、丙酮和几滴催化剂,在70℃条件下反应6h后,冷却到10℃出料;将预聚体用三乙胺中和加水进行高速乳化,然后加入乙二胺稀释液反应,得到水性聚氨酯乳液;将乳液减压蒸馏脱出丙酮即得环氧树脂用KH550开环改性水性聚氨酯涂料。
以上所述仅为本发明的较佳实施例,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 (4)
1.一种改进型涂料合成方法,其特征在于,包括如下步骤:
在干燥氮气的保护下, 将KH550和环氧树脂按计量加入四口瓶烧瓶中, 混合均匀后常温反应, 得到组分A;
在干燥氮气的保护下, 将真空脱水后的聚醚、组分A与IPDI按计量加入三口烧瓶中;
再加入计量好的一缩二乙二醇、TMP作交联剂、DM-PA、丙酮和几滴催化剂反应后出料;
将预聚体用三乙胺中和加水进行高速乳化, 然后加入乙二胺稀释液反应, 得到水性聚氨酯乳液;
将乳液减压蒸馏脱出丙酮即得环氧树脂用KH550开环改性水性聚氨酯涂料。
2.根据权利要求1所述一种改进型涂料合成方法,其特征在于,所述在干燥氮气的保护下, 将KH550和环氧树脂按计量加入四口瓶烧瓶中, 混合均匀后常温反应, 得到组分A步骤的具体实现如下:
在干燥氮气的保护下, 将KH550和环氧树脂按计量加入四口瓶烧瓶中, 混合均匀后常温反应1~5h, 得到组分A。
3. 根据权利要求1所述一种改进型涂料合成方法,其特征在于,所述在干燥氮气的保护下, 将真空脱水后的聚醚、组分A与IPDI按计量加入三口烧瓶中步骤的具体实现如下:
在干燥氮气的保护下, 将真空脱水后的聚醚、组分A与IPDI按计量加入三口烧瓶中,升温至85~90℃,反应1~2h。
4. 根据权利要求1所述一种改进型涂料合成方法,其特征在于,所述再加入计量好的一缩二乙二醇、TMP作交联剂、DM-PA、丙酮和几滴催化剂反应后出料步骤的具体实现如下:
再加入计量好的一缩二乙二醇、TMP作交联剂、DM-PA、丙酮和几滴催化剂,在60~70℃条件下反应1~6h后,冷却到40~10℃出料。
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Cited By (2)
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CN106117492A (zh) * | 2016-06-24 | 2016-11-16 | 安徽省思维新型建材有限公司 | 一种有机硅/环氧树脂改性聚氨酯的制备方法 |
WO2020121932A1 (ja) * | 2018-12-11 | 2020-06-18 | 三井化学株式会社 | ポリウレタンディスパージョンおよび積層体 |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
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CN106117492A (zh) * | 2016-06-24 | 2016-11-16 | 安徽省思维新型建材有限公司 | 一种有机硅/环氧树脂改性聚氨酯的制备方法 |
WO2020121932A1 (ja) * | 2018-12-11 | 2020-06-18 | 三井化学株式会社 | ポリウレタンディスパージョンおよび積層体 |
CN113039229A (zh) * | 2018-12-11 | 2021-06-25 | 三井化学株式会社 | 聚氨酯分散液及层叠体 |
JPWO2020121932A1 (ja) * | 2018-12-11 | 2021-10-07 | 三井化学株式会社 | ポリウレタンディスパージョンおよび積層体 |
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