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首页> 外文期刊>Iranian polymer journal >Synthesis, characterization, microstructure determination and thermal studies of poly(N-vinyl-2-pyrrolidone-maleic anhydride-styrene) terpolymer
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Synthesis, characterization, microstructure determination and thermal studies of poly(N-vinyl-2-pyrrolidone-maleic anhydride-styrene) terpolymer

机译:聚(N-乙烯基-2-吡咯烷酮-马来酸酐-苯乙烯)三元共聚物的合成,表征,微结构测定和热研究

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摘要

A series of poly(N-vinyl-2-pyrrolidone-maleic anhydride-styrene) terpolymers have been synthesized using titanium(Ⅲ)-dimethylglyoxime redox initiator system. The usage of redox initiators in the terpolymerization was limited; hence it should be considered as a new approach. The reactivity of the monomers has been studied by well-accepted Kelen-Tudos and Fineman-Ross linear methods and compared with the nonlinear RREVM method. The results also suggested that the RREVM method is the most reliable and superior method for the estimation of reactivity ratios. The reactivity ratios for the terpolymer (r_1 0.99 and r_2 0.05) obtained from the RREVM method showed that the N-vinyl pyrrolidone-maleic anhydride complex was more predominant than styrene in the terpolymer and the complex had more attraction toward itself than styrene. The microstructure determination study depicts that alternating polymer can be prepared by increasing the styrene feed content. The resonance factor and polarity of the complex were calculated as 5.01 and 0.93, respectively, which were different from those of the individual monomers. These calculations would help in predicting the association of monomers during copoly-merization. It was observed that the glass transition temperature of the terpolymer increased as the complex ratio in the terpolymer increased. The terpolymer was thermally; stable up to 323 ℃.
机译:利用钛(Ⅲ)-二甲基乙二肟肟氧化还原引发剂体系合成了一系列的聚(N-乙烯基-2-吡咯烷酮-马来酸酐-苯乙烯)三元共聚物。在三元聚合中氧化还原引发剂的使用受到限制;因此,应将其视为一种新方法。通过公认的Kelen-Tudos和Fineman-Ross线性方法研究了单体的反应性,并与非线性RREVM方法进行了比较。结果还表明,RREVM方法是估计反应率的最可靠,最优越的方法。通过RREVM方法获得的三元共聚物的反应率(r_1 0.99和r_2 0.05)表明,三元共聚物中的N-乙烯基吡咯烷酮-马来酸酐配合物比苯乙烯更占优势,并且该配合物比苯乙烯更具吸引力。微观结构测定研究表明,可以通过增加苯乙烯进料的含量来制备交替聚合物。计算出配合物的共振因子和极性分别为5.01和0.93,这与各个单体的共振因子和极性不同。这些计算将有助于预测共聚过程中单体的缔合。观察到,三元共聚物的玻璃化转变温度随着三元共聚物中的配合比的增加而增加。三元共聚物是热的。稳定在323℃。

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