CN106519929A - Uv固化防雾功能预聚物的制备方法 - Google Patents

Uv固化防雾功能预聚物的制备方法 Download PDF

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CN106519929A
CN106519929A CN201611008086.8A CN201611008086A CN106519929A CN 106519929 A CN106519929 A CN 106519929A CN 201611008086 A CN201611008086 A CN 201611008086A CN 106519929 A CN106519929 A CN 106519929A
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prepolymer
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李长英
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Shaanxi Jujiehan Chemical Co Ltd
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Abstract

本发明涉及新型化工材料技术领域,具体涉及一种UV固化防雾功能预聚物的制备方法。UV固化防雾功能预聚物的制备方法,包括如下步骤:(1)端羟基聚酯的合成;(2)预聚物的合成;(3)UV固化防雾涂料的制备。本发明制成的防雾功能预聚物,其具有良好的透光性能,膜性能依旧良好,热稳定性能有所提高,具有更广的适应性。

Description

UV固化防雾功能预聚物的制备方法
技术领域
本发明涉及新型化工材料技术领域,具体涉及一种UV固化防雾功能预聚物的制备方法。
背景技术
UV固化防雾涂料是一种新型的功能型绿色环保涂料,与传统的固化防雾涂料相比具有快速固化、环保、低耗能和成膜性能优异等特点,是新一代绿色化工产品,主要应用于汽车挡风玻璃、眼镜片、浴室镜和游泳镜等的防雾,因此已成为未来防雾涂料发展的一个趋势。目前对其研究主要集中解决防雾涂料的不耐水,防雾效果差,硬度及附着力不高等问题。
发明内容
本发明旨在提出一种UV固化防雾功能预聚物的制备方法。
本发明的技术方案在于:
UV固化防雾功能预聚物的制备方法,包括如下步骤:
(1)端羟基聚酯的合成
称取二甲苯、二缩三乙二醇、对甲苯磺酸和间苯二甲酸-5-磺酸钠置于带有搅拌器、分水器和冷凝装置的四口烧瓶中,搅拌并升温,待体系温度升至145℃,二甲苯开始回流,回流反应5-6h直至体系酸值小于5mgKOH/g,抽真空,脱除二甲苯,降温制得端羟基聚酯;
(2)预聚物的合成
称取步骤(1)中获得的端羟基聚酯、对甲苯磺酸、四甲氧基酚和二甲苯置于带有滴液漏斗、搅拌器、分水器和冷凝装置的四口烧瓶中,搅拌并升温,再称取MMA置于滴液漏斗中,开始滴加甲基丙烯酸, 1-1.5h内滴加完毕,继续反应3-4h,直至体系羟值小于10mgKOH/g,抽真空,降湿出料,真空干燥24h,最后得到透明的UV固化预聚物;
(3)UV固化防雾涂料的制备
将步骤(2)中获得的UV固化预聚物于引发剂、三羟甲基丙烷三丙烯酸酯再与1-甲基-2-吡咯烷酮均匀混合,于常温下搅拌约15min配制成涂料,涂覆于透明玻璃表面,并固化成膜,形成UV固化防雾功能预聚物。
所述的固化成膜在紫外灯的照射下完成。
所述的步骤(3)中搅拌时间为15min。
本发明的技术效果在于:
本发明制成的防雾功能预聚物,其具有良好的透光性能,膜性能依旧良好,热稳定性能有所提高,具有更广的适应性。
具体实施方式
UV固化防雾功能预聚物的制备方法,包括如下步骤:
(1)端羟基聚酯的合成
称取二甲苯、二缩三乙二醇、对甲苯磺酸和间苯二甲酸-5-磺酸钠置于带有搅拌器、分水器和冷凝装置的四口烧瓶中,搅拌并升温,待体系温度升至145℃,二甲苯开始回流,回流反应5-6h直至体系酸值小于5mgKOH/g,抽真空,脱除二甲苯,降温制得端羟基聚酯;
(2)预聚物的合成
称取步骤(1)中获得的端羟基聚酯、对甲苯磺酸、四甲氧基酚和二甲苯置于带有滴液漏斗、搅拌器、分水器和冷凝装置的四口烧瓶中,搅拌并升温,再称取MMA置于滴液漏斗中,开始滴加甲基丙烯酸, 1-1.5h内滴加完毕,继续反应3-4h,直至体系羟值小于10mgKOH/g,抽真空,降湿出料,真空干燥24h,最后得到透明的UV固化预聚物;
(3)UV固化防雾涂料的制备
将步骤(2)中获得的UV固化预聚物于引发剂、三羟甲基丙烷三丙烯酸酯再与1-甲基-2-吡咯烷酮均匀混合,于常温下搅拌约15min配制成涂料,涂覆于透明玻璃表面,并固化成膜,形成UV固化防雾功能预聚物。
所述的固化成膜在紫外灯的照射下完成。
所述的步骤(3)中搅拌时间为15min。
可知,预聚物对于波长在270~340nm的紫外光有不同程度的吸收作用,表明该预聚物对紫外光有屏蔽性能,因预聚物含有大量苯环结构。而在其他波段的透光率均高于90%,显示良好的透光性能。
预聚物的分解温度在225℃左右,显示良好的热稳定性;玻璃化转变温度在27℃左右,分子链有一定的柔韧性,表明该预聚物适合于制备UV固化防雾涂料。
预聚物的表面张力为16.5mN/m,由于UV固化预聚物是通过醇酸缩聚再酯化得到的并带有大量的亲水基团的一种线性水溶性聚合物,其表面张力的大小直接影响预聚物与涂料体系的相容性,制备UV固化防雾涂料不需外加其他助剂,成膜性能依旧良好。
由于体系存在部分未固化交联彻底的小分子单体造成TG曲线上有部分质量损失,温度在275℃以后损失的是已交联彻底的涂膜的质量,对比预聚物的热失重曲线发现,预聚物开始裂解的温度约为225℃,经交联固化得到的涂膜开始裂解温度约为275℃,表明经交联固化得到的涂膜热稳定性能有所提高,具有更广的适应性。本发明制成的防雾功能预聚物,其具有良好的透光性能,膜性能依旧良好,热稳定性能有所提高,具有更广的适应性。

Claims (3)

1.UV固化防雾功能预聚物的制备方法,其特征在于:包括如下步骤:
(1)端羟基聚酯的合成
称取二甲苯、二缩三乙二醇、对甲苯磺酸和间苯二甲酸-5-磺酸钠置于带有搅拌器、分水器和冷凝装置的四口烧瓶中,搅拌并升温,待体系温度升至145℃,二甲苯开始回流,回流反应5-6h直至体系酸值小于5mgKOH/g,抽真空,脱除二甲苯,降温制得端羟基聚酯;
(2)预聚物的合成
称取步骤(1)中获得的端羟基聚酯、对甲苯磺酸、四甲氧基酚和二甲苯置于带有滴液漏斗、搅拌器、分水器和冷凝装置的四口烧瓶中,搅拌并升温,再称取MMA置于滴液漏斗中,开始滴加甲基丙烯酸, 1-1.5h内滴加完毕,继续反应3-4h,直至体系羟值小于10mgKOH/g,抽真空,降湿出料,真空干燥24h,最后得到透明的UV固化预聚物;
(3)UV固化防雾涂料的制备
将步骤(2)中获得的UV固化预聚物于引发剂、三羟甲基丙烷三丙烯酸酯再与1-甲基-2-吡咯烷酮均匀混合,于常温下搅拌约15min配制成涂料,涂覆于透明玻璃表面,并固化成膜,形成UV固化防雾功能预聚物。
2.根据权利要求1所述的UV固化防雾功能预聚物的制备方法,其特征在于:所述的固化成膜在紫外灯的照射下完成。
3.根据权利要求1所述的UV固化防雾功能预聚物的制备方法,其特征在于:所述的步骤(3)中搅拌时间为15min。
CN201611008086.8A 2016-11-16 2016-11-16 Uv固化防雾功能预聚物的制备方法 Pending CN106519929A (zh)

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Application publication date: 20170322