Radical Polymerization Kinetics of Hexyl Methacrylate in Dimethylsulfoxide Solution

Hala Rahman Noormohamad, Ameen Hadi
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Abstract

In this study, we conducted a series of polymerization studies of hexyl methacrylate in dimethyl sulfoxide with (0.1 - 0.4) mol dm-3 of monomer and (1 10-3 – 4 10-3) mol dm-3 of benzoyl peroxide as initiators at 70 °C. Using the well-known conversion vs. time technique, the effects of initiator and monomer concentration on the rate of polymerization (Rp) were studied. An initiator of order 0.35 was obtained in accordance with theory and a divergence from normal kinetics was detected with an order of 1.53 with respect to monomer concentration. The activation energy was determined to be (72.90) kJ mol-1, which does not correspond to the value of most thermally initiated monomers. The observed value of activation energy suggests that propagation and termination reactions have equal activation energy and the difference between them is nearly zero. The average degree of polymerization (DPn) decreased as benzoyl peroxide concentration increase whereas an increase in solvent polarity has slightly increased rate of polymerization value.
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甲基丙烯酸己酯在二甲亚砜溶液中的自由基聚合动力学
在本研究中,我们以(0.1 - 0.4)mol dm-3单体和(1 10-3 - 4 10-3)mol dm-3过氧化苯甲酰为引发剂,在70℃下进行了一系列甲基丙烯酸己酯在二甲亚砜中的聚合研究。采用著名的转化率-时间法,研究了引发剂和单体浓度对聚合速率的影响。根据理论得到了0.35阶的引发剂,并检测到单体浓度与正常动力学的差异,其阶数为1.53。测定的活化能为(72.90)kJ mol-1,不符合大多数热引发单体的值。活化能的观测值表明,传播反应和终止反应具有相等的活化能,两者之间的差值几乎为零。平均聚合度(DPn)随过氧化苯甲酰浓度的增加而降低,而溶剂极性的增加使聚合速率值略有增加。
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审稿时长
18 weeks
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