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Effect of Graphene oxide or Functionalized Graphene Oxide on the Copolymerization Kinetics of Styrene-butyl Methacrylate

机译:氧化石墨烯或官能化氧化石墨烯对苯乙烯/甲基丙烯酸正丁酯共聚动力学的影响

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摘要

Nanocomposite materials based on copolymers of styrene and n-butyl methacrylate with either graphene oxide (GO) or functionalized graphene oxide (F-GO) were synthesized using the in-situ bulk radical copolymerization technique. Reaction kinetics was studied both experimentally and theoretically using a detailed kinetic model also taking into account the effect of diffusion-controlled phenomena on the reaction kinetic rate constants. It was found that the presence of GO results in lower polymerization rates accompanied by the synthesis of copolymers having higher average molecular weights. In contrast, the presence of F-GO did not seem to significantly alter the conversion vs time curves, whereas it results in slightly lower average molecular weights. The first observation was attributed to side reactions of the initiator primary radicals with the hydroxyl groups on the surface of GO, resulting in lower initiator efficiency, whereas the second to grafted structures formed from copolymer macromolecules on the F-GO surface. The copolymerization model predictions including MWD data were found to be in satisfactory agreement with the experimental data. At least four adjustable parameters were employed and their best-fit values were provided.
机译:使用原位本体自由基共聚合技术合成了基于苯乙烯和甲基丙烯酸正丁酯与氧化石墨烯(GO)或功能化氧化石墨烯(F-GO)的共聚物的纳米复合材料。使用详细的动力学模型对反应动力学进行了实验和理论研究,同时考虑了扩散控制现象对反应动力学速率常数的影响。已经发现GO的存在导致较低的聚合速率,同时合成具有较高平均分子量的共聚物。相比之下,F-GO的存在似乎并没有明显改变转化率与时间的关系曲线,但是却导致平均分子量略低。第一个观察结果归因于引发剂伯自由基与GO表面的羟基发生副反应,导致引发剂效率降低,而第二个观察则归因于F-GO表面上由共聚物大分子形成的接枝结构。发现包括MWD数据的共聚模型预测与实验数据令人满意。至少使用四个可调参数,并提供它们的最佳拟合值。

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