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硅氧烷封端水性含氟聚氨酯的制备及性能研究 被引量:1

Preparation and properties of siloxane-terminated waterborne fluorinated polyurethane
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摘要 采用1-巯基甘油(MTG)和2-(全氟己基)乙基甲基丙烯酸酯(PFOL)之间的硫醇-烯点击反应自制含氟二元醇(PFOH);采用烯丙基羟乙基醚(AYEL)和三甲氧基硅烷(TMS)间的硅氢加成反应自制单端含C-OH的硅氧烷(TMSO);将所得产物引入到聚氨酯体系中,得到一系列硅氧烷封端的水性含氟聚氨酯(WFSiPU)。结合FT-IR和^(1)H-NMR对产物的结构进行表征,通过紫外可见近红外分光光度计、光学接触角测量仪和热重分析仪等表征仪器探究PFOH和TMSO对水性聚氨酯各项性能的影响。结果表明,随着水性聚氨酯体系中PFOH和TMSO的引入,乳液粒径逐渐增大,分布变宽,涂膜的热稳定性、力学性能、疏水性、耐水性等性能均得到了明显改善。当PFOH添加量为8%,TMSO添加量为50%时,涂膜整体综合性能最佳。 Fluorinated dihydric alcohols(PFOH)were prepared by mercapto-ene click reaction between 1-mercaptoglycerol(MTG)and 2-(perfluorohexyl)ethyl methacrylate(PFOL).Siloxane(TMSO)containing C-OH was produced by hydrosilylation reaction between allyl hydroxyethyl ether(AYEL)and trimethoxysilane(TMS).A series of siloxane-terminated waterborne fluorinated polyurethanes(WFSiPU)were obtained by introducing the products into polyurethane system.The structures of these products were characterized by FT-IR and ^(1)H-NMR,and the effects of PFOH and TMSO on the properties of waterborne polyurethanes were investigated by UV-visible nearinfrared spectrophotometer,optical contact angle measuring instrument and thermogravimetric analyzer.The results showed that,with the introduction of PFOH and TMSO in the waterborne polyurethane system,the particle size of the emulsion gradually increased,the distribution became wider,and the thermal stability,mechanical properties,hydrophobicity,water resistance and other properties of the film were obviously improved.When the addition amount of PFOH was 8%and TMSO was 50%,the overall performance of the film was the best.
作者 王宇通 陈欢 姚伯龙 倪亚洲 王海潮 张晋瑞 Wang Yutong;Chen Huan;Yao Bolong;Ni Yazhou;Wang Haichao;Zhang Jinrui(Key Laboratory of Synthetic and Biological Colloids of Ministry of Education,Jiangnan University,Wuxi 214122;School of Chemistry and Material Engineering,Jiangnan University,Wuxi 214122)
出处 《化工新型材料》 CAS CSCD 北大核心 2023年第3期147-154,共8页 New Chemical Materials
关键词 含氟聚氨酯 硅氧烷硫醇 硫醇-烯点击反应 硅氢加成 fluorinated polyurethane oxosilane mercaptan-ene click reaction hydrosilylation
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