CN115074014B - 一种非氟无痕抗污水性聚氨酯自分层涂料的制备方法 - Google Patents

一种非氟无痕抗污水性聚氨酯自分层涂料的制备方法 Download PDF

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CN115074014B
CN115074014B CN202210712054.5A CN202210712054A CN115074014B CN 115074014 B CN115074014 B CN 115074014B CN 202210712054 A CN202210712054 A CN 202210712054A CN 115074014 B CN115074014 B CN 115074014B
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方华高
高星辰
周文娟
宋楷
丁运生
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Abstract

本发明涉及一种非氟无痕抗污水性聚氨酯自分层涂料的制备方法,属于聚氨酯涂料领域技术领域。操作步骤如下:将4,4'‑二环己基甲烷二异氰酸酯、聚四氢呋喃二醇和聚二甲基硅氧烷二醇在氮气保护下机械搅拌反应,获得异氰酸酯封端的预聚体;加入亲水扩链剂和二月桂酸二丁基锡反应,再加入受阻型二胺反应;降至室温,加入三乙胺中和,加入去离子水乳化,获得水性聚氨酯涂料。将水性聚氨酯涂料涂至基材表面,熟化,得到水性聚氨酯涂层。基于可逆共价键接的亲疏水链段展现出“原位解离—聚合”和亲—疏水组分相分离的双重动力学机制,为水性聚氨酯涂层创造了自分层条件,提高水性聚氨酯涂层抗污疏水性能、强韧性和能力,水性聚氨酯涂层的水接触角大于150°。

Description

一种非氟无痕抗污水性聚氨酯自分层涂料的制备方法
技术领域
本发明属于聚氨酯涂料技术领域,具体涉及了一种非氟无痕抗污水性聚氨酯自分层涂料的制备方法。
背景技术
“双碳”目标的提出将我国的绿色发展之路提升到新的高度。具有自清洁特性的无痕抗污涂层在家用电器、消费电子和其他工业装备等领域都有广泛的需求,是近年发展迅速的新涂料种类,受到产业界和消费者的持续关注和青睐。目前大多数无痕抗污涂料以有机溶剂为分散介质,采用含氟材料为疏水成分如“自修复性涂料组合物、自修复性涂层、含有该自修复性涂层的保护膜及其应用” ,虽然该涂料拥有良好的自修复性能,然而有机溶剂的挥发性和长链全氟烷基物质具有持久性、生物累积性和毒性,都给无痕抗污涂料的发展带来极大隐患,美国环保署和欧盟机构颁布严格的法规,限制含氟树脂和材料的使用,我国的立法限制也已呼之欲出,迫切需要开发环境友好型的非氟无痕抗污水性涂料。
发明内容
针对含氟材料的生物毒性、VOC挥发的污染和表面涂层易刮损,寿命短等问题,本发明提供了一种非氟无痕抗污水性聚氨酯自分层涂料,另一方面,本发明提供了一种非氟无痕抗污水性聚氨酯自分层涂料的制备方法。
一种非氟无痕抗污水性聚氨酯自分层涂料的制备操作步骤如下:
(1)水性聚氨酯涂料的制备
首先将1mol4,4'-二环己基甲烷二异氰酸酯、0.2~0.4mol聚四氢呋喃二醇和0.2~0.4mol聚二甲基硅氧烷二醇在氮气保护下,温度80℃机械搅拌反应2h,获得异氰酸酯封端的预聚体;加入0.2mol亲水扩链剂2,2-二羟甲基丙酸和0.002mol二月桂酸二丁基锡(DBTAL)反应2h进行扩链,然后加入0.2~0.4mol受阻型二胺N-(3-二甲基氨基丙基)-N, N-二异丙醇胺(TBEU)继续反应2h;将反应降至室温,之后加入0.2mol三乙胺进行中和,最后加入1000g去离子水在2000 rpm的转速下搅拌1h进行乳化,乳化条件为转速1500~2000 rpm,获得水性聚氨酯涂料;
所述水性聚氨酯涂料的pH值为7~9,粒径≤300 nm;
所述聚四氢呋喃二醇重均分子量 M w=1000 g/mol;
所述聚二甲基硅氧烷二醇的重均分子量 M w=1000 g/mol;
(2)涂覆使用
首先,在基材表面上喷洒乙醇清洗,室温下晾干;将水性聚氨酯涂料涂至清洗过的基材表面;将基材在温度50~100℃环境下,熟化72h,得到水性聚氨酯涂层,水性聚氨酯涂层的厚度为20~40μm;
疏水性测试表明,水性聚氨酯涂层的水接触角大于150°。
步骤(2)中,所述基材为聚甲基丙烯酸甲酯(PMMA)、聚对苯二甲酸乙二醇酯(PET)、聚氯乙烯(PVC)、聚丙烯(PP)、聚碳酸酯(PC)、铁、铝、不锈钢中的一种。
与已有技术相比,本发明的有益技术效果体现在以下方面:
(1)通过在脲键的一个氮原子上引入大取代基,生成的受阻脲键在无催化剂条件下发生可逆的解离与结合,水性聚氨酯涂料表现出良好的自修复性质,提高其耐磨性。本发明的水性聚氨酯涂料用铜刷形成受损表面后10min内,实现快速修复不留痕迹。
(2)在高于60℃的条件下,受阻脲键会发生可逆的解离,可逆共价键接的亲疏水链段将展现出“原位解离—聚合”和亲—疏水组分相分离的双重动力学机制,低表面能的疏水PDMS离解并迁移到涂层表面,使水性聚氨酯产生自分层效果,进而达到抗污水的效果。本发明的水性聚氨酯涂料水接触角均高于150°,且油性笔痕迹用乙醇擦拭后未留下任何污渍,展现出良好的疏水抗污性能。
(3)本发明使用无氟原料设计水性聚氨酯涂料的开发使用,对环境有益,在无痕抗污涂料领域可实现高性能化及低碳环保,符合“双碳”目标理念。
具体实施方式
下面通过实施例对本发明作进一步地详细说明。
以下实施例中所用原料说明如下:
4,4'-二环己基甲烷二异氰酸酯(HDMI)购自巴斯夫股份公司;
聚四氢呋喃二醇(PTMG)购自日本三菱化工股份有限公司;
聚二甲基硅氧烷二醇(PDMS)购自美国Gelest股份有限公司;
二月桂酸二丁基锡(DBTAL),2,2-二羟甲基丙酸(DMPA)和1,4-丁二醇(BDO)均购自阿拉丁试剂有限公司;
N-(3-二甲基氨基丙基)-N, N-二异丙醇胺(TBEU)购自麦卡希化工有限公司。
实施例1
一种非氟无痕抗污水性聚氨酯自分层涂料制备操作步骤如下:
(1)水性聚氨酯涂料的制备
首先将262g 4,4'-二环己基甲烷二异氰酸酯(1mol)、400g聚四氢呋喃二醇(0.4mol)和200g聚二甲基硅氧烷二醇(0.2mol)在氮气保护下,温度80℃机械搅拌反应2h,获得异氰酸酯封端的预聚体;加入29.6g亲水扩链剂2,2-二羟甲基丙酸(0.2mol)和1.26g二月桂酸二丁基锡(0.002mol)反应2h进行扩链,然后加入43.6g受阻型二胺N-(3-二甲基氨基丙基)-N, N-二异丙醇胺(0.2mol)继续反应2h;将反应降至室温,之后加入20.2g三乙胺(0.2mol)进行中和,最后加入1000g去离子水在2000 rpm的转速下搅拌1h进行乳化,获得水性聚氨酯涂料;
所述水性聚氨酯涂料的pH值为8,粒径≤180 nm;
(2)涂覆使用
首先,在聚对苯二甲酸乙二醇酯基材表面上喷洒乙醇清洗,室温下晾干;将水性聚氨酯涂料涂至清洗过的聚对苯二甲酸乙醇二酯基材表面;将聚对苯二甲酸乙二醇酯基材在温度50℃环境下,熟化72h,得到水性聚氨酯涂料的涂层厚度为40μm。
1.损伤修复性能测试
测试方法:市售黄铜刷,加荷重1公斤,在涂层面上往复10次后,将样品放在70℃的烘箱中,观察损伤表面是否能恢复,同时记录恢复所用时间。
2. 疏水性能测试
测试方法:在25℃下用接触角测量仪测量样品的疏水性能,介质为去离子水。在每组样品的5个不同位置上,测试其水接触角,去掉最高值和最低值,取剩余数的平均值。
3. 耐污性能测试
(1)测试方法
用油性笔在水性聚氨酯涂层划出明显笔痕,然后用乙醇擦拭水性聚氨酯涂层,擦拭后观察水性聚氨酯涂层表面是否留有明显污痕。
本实施例1制得的水性聚氨酯涂层在铜刷刷过后10min内可以快速修复不留痕迹,表现出良好的损伤修复性能。疏水性测试表明,水性聚氨酯涂层的水接触角为152°,水性聚氨酯涂层油性笔痕迹用乙醇擦拭后未留下任何污渍,展现出良好的疏水抗污性能。
实施例2
一种非氟无痕抗污水性聚氨酯自分层涂料制备操作步骤如下:
(1)水性聚氨酯涂料的制备
首先将262g 4,4'-二环己基甲烷二异氰酸酯(1mol)、300g 聚四氢呋喃二醇(0.3mol)和300g 聚二甲基硅氧烷二醇(0.3mol),在氮气保护下,温度80℃机械搅拌反应2h,获得异氰酸酯封端的预聚体;加入亲水扩链剂29.6g 2,2-二羟甲基丙酸(0.2mol)和1.26g二月桂酸二丁基锡(0.002mol)反应2h进行扩链,然后加入43.6g受阻型二胺N-(3-二甲基氨基丙基)-N, N-二异丙醇胺(0.2mol)继续反应2h;将反应降至室温,之后加入20.2g三乙胺(0.2mol)进行中和,最后加入1000g去离子水在2000 rpm的转速下搅拌1h进行乳化,获得水性聚氨酯涂料;
所述水性聚氨酯涂料的pH值为7,粒径≤240 nm;
(2)涂覆使用
首先,在聚对苯二甲酸乙二醇酯基材表面上喷洒乙醇清洗,室温下晾干;将水性聚氨酯涂料涂至清洗过的聚对苯二甲酸乙二醇酯基材表面;将聚对苯二甲酸乙二醇酯基材在温度70℃环境下,熟化72h,得到水性聚氨酯涂料的涂层厚度为40μm。
本实施例2制得的水性聚氨酯涂层在铜刷刷过后8min内可以快速修复不留痕迹,表现出良好的损伤修复性能。疏水性测试表明,水性聚氨酯涂层的水接触角为168°,水性聚氨酯涂层油性笔痕迹用乙醇擦拭后未留下任何污渍,展现出良好的疏水抗污性能。
实施例3
一种非氟无痕抗污水性聚氨酯自分层涂料制备操作步骤如下:
(1)水性聚氨酯涂料的制备
首先将262g 4,4'-二环己基甲烷二异氰酸酯(1mol),200g 聚四氢呋喃二醇(0.2mol)和400g 聚二甲基硅氧烷二醇(0.4mol)在氮气保护下,温度80℃机械搅拌反应2h,获得异氰酸酯封端的预聚体;加入29.6g亲水扩链剂2,2-二羟甲基丙酸(0.2mol)和1.26g二月桂酸二丁基锡(0.002mol)反应2h进行扩链,然后加入43.6g受阻型二胺N-(3-二甲基氨基丙基)-N, N-二异丙醇胺(0.2mol)继续反应2h;将反应降至室温,之后加入20.2g三乙胺(0.2mol)进行中和,最后加入1000g去离子水在2000 rpm的转速下搅拌1h进行乳化,获得水性聚氨酯涂料;
所述水性聚氨酯涂料的pH值为9,粒径≤300 nm;
(2)涂覆
首先,在聚对苯二甲酸乙二醇酯基材表面上喷洒乙醇清洗,室温下晾干;将水性聚氨酯涂料涂至清洗过的聚对苯二甲酸乙二醇酯基材表面;将聚对苯二甲酸乙二醇酯基材在温度70℃环境下,熟化72h,得到水性聚氨酯涂料的涂层厚度为40μm。
本实施例3制得的水性聚氨酯涂层在铜刷刷过后8min内可以快速修复不留痕迹,表现出良好的损伤修复性能。疏水性测试表明,水性聚氨酯涂层的水接触角为172°,水性聚氨酯涂层油性笔痕迹用乙醇擦拭后未留下任何污渍,展现出良好的疏水抗污性能。
实施例4
一种非氟无痕抗污水性聚氨酯自分层涂料制备操作步骤如下:
(1)水性聚氨酯涂料的制备
首先将262g 4,4'-二环己基甲烷二异氰酸酯(1mol),200g 聚四氢呋喃二醇(0.2mol)和200g 聚二甲基硅氧烷二醇(0.2mol)在氮气保护下,温度80℃机械搅拌反应2h,获得异氰酸酯封端的预聚体;加入29.6g亲水扩链剂2,2-二羟甲基丙酸(0.2mol)和1.26g二月桂酸二丁基锡(0.002mol)反应2h进行扩链,然后加入87.2g受阻型二胺N-(3-二甲基氨基丙基)-N, N-二异丙醇胺(0.4mol)继续反应2h;将反应降至室温,之后加入20.2g三乙胺(0.2mol)进行中和,最后加入1000g去离子水在2000 rpm的转速下搅拌1h进行乳化,获得水性聚氨酯涂料;
所述水性聚氨酯涂料的pH值为8,粒径≤180 nm;
(2)涂覆
首先,在聚对苯二甲酸乙二醇酯基材表面上喷洒乙醇清洗,室温下晾干;将水性聚氨酯涂料涂至清洗过的聚对苯二甲酸乙二醇酯基材表面;将聚对苯二甲酸乙二醇酯基材在温度70℃环境下,熟化72h,得到水性聚氨酯涂料的涂层厚度为40μm。
本实施例4制得的水性聚氨酯涂层在铜刷刷过后5 min内可以快速修复不留痕迹,表现出良好的损伤修复性能。疏水性测试表明,水性聚氨酯涂层的水接触角为163°,水性聚氨酯涂层油性笔痕迹用乙醇擦拭后未留下任何污渍,展现出良好的疏水抗污性能。
实施例5
一种非氟无痕抗污水性聚氨酯自分层涂料制备操作步骤如下:
(1)水性聚氨酯涂料的制备
首先将262g 4,4'-二环己基甲烷二异氰酸酯(1mol),300g 聚四氢呋喃二醇(0.3mol)和200g 聚二甲基硅氧烷二醇(0.2mol)在氮气保护下,温度80℃机械搅拌反应2h,获得异氰酸酯封端的预聚体;加入29.6g亲水扩链剂2,2-二羟甲基丙酸(0.2mol)和1.26g二月桂酸二丁基锡(0.002mol)反应2h进行扩链,然后加入65.4g受阻型二胺N-(3-二甲基氨基丙基)-N, N-二异丙醇胺(0.3mol)继续反应2h;将反应降至室温,之后加入20.2g三乙胺(0.2mol)进行中和,最后加入1000g去离子水在2000 rpm的转速下搅拌1h进行乳化,获得水性聚氨酯涂料;
所述水性聚氨酯涂料的pH值为8,粒径≤180 nm;
(2)涂覆
首先,在聚对苯二甲酸乙二醇酯基材表面上喷洒乙醇清洗,室温下晾干;将水性聚氨酯涂料涂至清洗过的聚对苯二甲酸乙二醇酯基材表面;将聚对苯二甲酸乙二醇酯基材在温度90℃环境下,熟化72h,得到水性聚氨酯涂料的涂层厚度为40μm。
本实施例5制得的水性聚氨酯涂层在铜刷刷过后4 min内可以快速修复不留痕迹,表现出良好的损伤修复性能。疏水性测试表明,水性聚氨酯涂层的水接触角为165°,水性聚氨酯涂层油性笔痕迹用乙醇擦拭后未留下任何污渍,展现出良好的疏水抗污性能。
实施例6
一种非氟无痕抗污水性聚氨酯自分层涂料制备操作步骤如下:
(1)水性聚氨酯涂料的制备
首先262g 4,4'-二环己基甲烷二异氰酸酯(1mol),200g 聚四氢呋喃二醇(0.2mol)和300g 聚二甲基硅氧烷二醇(0.3mol)在氮气保护下,温度80℃机械搅拌反应2h,获得异氰酸酯封端的预聚体;加入29.6g亲水扩链剂2,2-二羟甲基丙酸(0.2mol)和1.26g二月桂酸二丁基锡(0.002mol)反应2h进行扩链,然后加入65.4g受阻型二胺N-(3-二甲基氨基丙基)-N, N-二异丙醇胺(0.3mol)继续反应2h;将反应降至室温,之后加入20.2g三乙胺(0.2mol)进行中和,最后加入1000g去离子水在2000 rpm的转速下搅拌1h进行乳化,获得水性聚氨酯涂料;
所述水性聚氨酯涂料的pH值为7,粒径≤230 nm;
(2)涂覆
首先,在聚对苯二甲酸乙二醇酯基材表面上喷洒乙醇清洗,室温下晾干;将水性聚氨酯涂料涂至清洗过的聚对苯二甲酸乙二醇酯基材表面;将聚对苯二甲酸乙二醇酯基材在温度90℃环境下,熟化72h,得到水性聚氨酯涂料的涂层厚度为40μm。
本实施例6制得的水性聚氨酯涂层在铜刷刷过后4min内可以快速修复不留痕迹,表现出良好的损伤修复性能。疏水性测试表明,水性聚氨酯涂层的水接触角为169°,水性聚氨酯涂层油性笔痕迹用乙醇擦拭后未留下任何污渍,展现出良好的疏水抗污性能。
对比例1
采用1,4-丁二醇(BDO)代替受阻性二胺N-(3-二甲基氨基丙基)-N,N-二异丙醇胺(TBEU)。
(1)水性聚氨酯涂料的制备
首先262g 4,4'-二环己基甲烷二异氰酸酯(1mol),400g 聚四氢呋喃二醇(0.4mol)和200g 聚二甲基硅氧烷二醇(0.2mol)在氮气保护下,温度80℃机械搅拌反应2h,获得异氰酸酯封端的预聚体;之后加入29.6g亲水扩链剂2,2-二羟甲基丙酸(0.2mol)和1.26g 二月桂酸二丁基锡(0.002mol)反应2h进行扩链,然后加入18g 1,4-丁二醇(0.2mol)继续反应2h;将反应降至室温,之后加入20.2g三乙胺(0.2mol)进行中和,最后加入1000g去离子水在2000 rpm的转速下搅拌1h进行乳化,获得水性聚氨酯涂料;
(2)涂覆
首先,在聚对苯二甲酸乙二醇酯基材表面上喷洒乙醇清洗,室温下晾干;将水性聚氨酯涂料涂至清洗过的聚对苯二甲酸乙二醇酯基材表面;将聚对苯二甲酸乙二醇酯基材在温度50℃环境下,熟化72h,得到水性聚氨酯涂料的涂层厚度为40μm。
本对比例1制得的水性聚氨酯涂层在铜刷刷过后无法修复,损伤修复性能差。疏水性测试表明,水性聚氨酯涂层的水接触角为110°,水性聚氨酯涂层油性笔痕迹用乙醇擦拭后留下少量污渍。
对实施例和对比例制备的水性聚氨酯涂料的性能进行检测。测试结果如表1所示。
本领域的技术人员容易理解,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、等同替换和改进等,均应包含在本发明的保护范围之内。

Claims (2)

1. 一种非氟无痕抗污水性聚氨酯自分层涂料的制备方法,其特征在于,操作步骤如下:
(1)水性聚氨酯涂料的制备
首先将1mol4,4'-二环己基甲烷二异氰酸酯、0.2~0.4mol聚四氢呋喃二醇和0.2~0.4mol聚二甲基硅氧烷二醇在氮气保护下,温度80℃机械搅拌反应2h,获得异氰酸酯封端的预聚体;加入0.2mol亲水扩链剂2,2-二羟甲基丙酸和0.002mol二月桂酸二丁基锡反应2h进行扩链,然后加入0.2~0.4mol受阻型二胺N-(3-二甲基氨基丙基)-N, N-二异丙醇胺继续反应2h;将反应降至室温,之后加入0.2mol三乙胺进行中和,最后加入1000g去离子水在2000 rpm的转速下搅拌1h进行乳化,乳化条件为转速1500~2000 rpm,获得水性聚氨酯涂料;
所述水性聚氨酯涂料的pH值为7~9,粒径≤300 nm;
所述聚四氢呋喃二醇重均分子量M w=1000 g/mol;
所述聚二甲基硅氧烷二醇的重均分子量M w=1000 g/mol;
(2)涂覆使用
首先,在基材表面上喷洒乙醇清洗,室温下晾干;将水性聚氨酯涂料涂至清洗过的基材表面;将基材在温度50~100℃环境下,熟化72h,得到水性聚氨酯涂层,水性聚氨酯涂层的厚度为20~40μm;
疏水性测试表明,水性聚氨酯涂层的水接触角大于150°。
2.根据权利要求1所述的一种非氟无痕抗污水性聚氨酯自分层涂料的制备方法,其特征在于:步骤(2)中,所述基材为聚甲基丙烯酸甲酯、聚对苯二甲酸乙二醇酯、聚氯乙烯、聚丙烯、聚碳酸酯、铁、铝、不锈钢中的一种。
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