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Hydrophilic Modification of Poly(vinylidene fluoride) via Atom transfer Radical Polymerization of 3-(Trimethoxysilyl)propyl Methacrylate

机译:通过原子转移自由基聚合的聚(偏二氟乙烯氟乙烯)的亲水改性3-(三甲氧基甲硅烷基)丙烯酸丙酯

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PVDF was modified by atom transfer radical polymerization (ATRP) directly from the secondary fluoride group of PVDF backbone. 3-(trimethoxysilyl) propyl methacrylate (TMSPMA) was initiated to polymerization by copper (I) chloride (CuCl) and 4,4'-dimethyl-2,2'-dipyridyl (DMDP) in a N-methyl pyrrolidinone (NMP) solution under an argon atmosphere. Spectra of NMR and FTIR-ATR on the grafted polymers showed that poly-(PTMSPMA) (PTMSPMA) side chains were successfully grafted to the PVDF backbone. Hydrolysis of the films prepared from the modified PVDF resulted in a reduction of contact angle, indicating their increased hydrophilicity. This modified PVDF with amphiphilicity and functional silyl groups would be a promising material for novel membrane separation applications.
机译:通过原子转移自由基聚合(ATRP)改性PVDF从PVDF骨架的二次氟化物基团进行修饰。将3-(三甲氧基甲硅烷基)丙基丙烯酸丙酯(TMSPMA)引发为通过铜(I)氯化物(CuCl)和4,4'-二甲基-2,2'-双二吡啶(DMDP)在N-甲基吡咯烷(NMP)溶液中的聚合在氩气氛下。接枝聚合物上的NMR和FTIR-ATR的光谱表明,聚 - (PTMSPMA)(PTMSPMA)侧链成功接枝到PVDF骨架上。由改性PVDF制备的膜的水解导致接触角的降低,表明它们增加了亲水性。这种具有两亲性和功能性甲硅烷基的改性的PVDF是用于新型膜分离应用的有希望的材料。

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