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The modification of butadiene-acrylonitrile rubber with vinylcyclohexyl ketone

机译:用乙烯基环己基酮改性丁二烯-丙烯腈橡胶

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Butadiene-acrylonitrile-vinylcyclohexyl ketone (BD-AN-VCHK) terpolymer was synthesized by radical polymerization. The structure of the synthesized terpolymer was elucidated by IR spectroscopy and physical and mechanical tests. BD-AN-VCHK terpolymer was stablest lower temperatures and exhibited goad adhesive properties. It was also observed that the yield of terpolymer was dependent upon the initial concentration of VCHK and pH of the media. The percentage of conversion increased by increasing the initial concentration of VCHK. With addition of 10.8% VCHK to the BD-AN mixture, the glass transition temperature (T{sub}g) value of the polymers decreased from -40℃ to -57℃. However further increase of VCHK ratio (20.4%) resulted in the formation of the polymers with T{sub}g value of -48℃. It was shown that this was due to the fact that VCHK, entering the structure during polymerization process, converted the trans structure of butadiene sequences into the cis form.
机译:通过自由基聚合反应合成了丁二烯-丙烯腈-乙烯基环己基酮(BD-AN-VCHK)三元共聚物。合成的三元共聚物的结构通过红外光谱和物理和机械测试得以阐明。 BD-AN-VCHK三元共聚物在较低的温度下最稳定,并显示出刺胶粘合性能。还观察到三元共聚物的产率取决于VCHK的初始浓度和培养基的pH。转化百分比通过增加VCHK的初始浓度而增加。在BD-AN混合物中加入10.8%的VCHK,聚合物的玻璃化转变温度(T {sub} g)从-40℃降至-57℃。然而,VCHK比率(20.4%)的进一步提高导致形成了T {sub} g值为-48℃的聚合物。结果表明,这是由于VCHK在聚合过程中进入结构,将丁二烯序列的反式结构转化为顺式。

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