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Radiation induced graft copolymerization of n-butyl acrylate onto poly(ethylene terephthalate) (PET) films and thermal properties of the obtained graft copolymer

机译:丙烯酸正丁酯在聚对苯二甲酸乙二醇酯(PET)薄膜上的辐射诱导接枝共聚反应及所得接枝共聚物的热性能

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摘要

n-Butyl acrylate (BA) was successfully grafted onto poly(ethylene terephthalate) (PET) film using simultaneous radiation induced graft copolymerization with gamma rays. When BA concentration ranges from 20% to 30%, the Degree of Grafting (DG), measured by gravimetry and ~1H NMR, increases with the monomer concentration and absorbed dose, but decreases with dose rate from 0.83 to 2.53 kGy/h. The maximum DG can reach up to 22.1%. The thermal transition temperatures such as glass-transition temperature (T_g) and cold-crystallization temperature (T_(cc)) of PET in grafted films were little different from those in original PET film, indicating that microphase separation occurred between PBA side chains and PET backbone. This work implied that if PET/elastomers (e.g., acrylate rubber) blends are radiated by high energy gamma rays under a certain condition, PET-g-polyacrylate copolymer may be produced in-situ, which will improve the compatibility between PET and the elastomers so as to improve the integral mechanical properties of PET based engineering plastic.
机译:丙烯酸正丁酯(BA)通过同时辐射诱发的γ射线接枝共聚反应成功地接枝到了聚对苯二甲酸乙二醇酯(PET)薄膜上。当BA浓度在20%至30%范围内时,通过重量分析和〜1H NMR测得的接枝度(DG)随着单体浓度和吸收剂量的增加而增加,但随剂量率从0.83至2.53 kGy / h降低。最高DG可达22.1%。接枝薄膜中PET的玻璃化转变温度(T_g)和冷结晶温度(T_(cc))等热转变温度与原始PET薄膜几乎没有差异,表明PBA侧链与PET之间发生了微相分离骨干。这项工作表明,如果在一定条件下通过高能伽马射线辐射PET /弹性体(例如丙烯酸酯橡胶)混合物,则可以原位生产PET-g-聚丙烯酸酯共聚物,这将改善PET与弹性体之间的相容性从而提高PET基工程塑料的整体力学性能。

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