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MULTI-SITE PHASE TRANSFER CATALYZED RADICAL POLYMERIZATION OF n-BUTYL METHACRYLATE: A KINETIC STUDY

机译:多位相转移催化甲基丙烯酸正丁酯的自由基聚合动力学研究

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摘要

The kinetics and mechanism of radical polymerization of n-butyl methacrylate (n-BMA) using potassium peroxydisulfate (PDS) as a water-soluble initiator in the presence of 1,4-bis(tributyl methyl ammonium) benzene dichloride (TBMABDC) as a multi-site phase transfer catalyst (MPTC) were studied. The polymerization reactions were carried out under oxygen-free, unstirred conditions at a constant temperature of 60° ± 1°C in cyclohexane-water two-phase systems. The dependence of rate of polymerization (Rp) on concentrations of monomer, initiator, and catalyst, volume fraction of aqueous phase, solvent polarity, and temperature was determined. The reaction order with respect to monomer, initiator, and multi-site phase transfer catalyst was found to be 0.50, 1.0, and 0.52 respectively. Based on the experimental results, an appropriate reaction mechanism has been proposed and its significance discussed. The prepared polymer was characterized with spectral analysis.
机译:在1,4-双(三丁基甲基铵)苯二氯化物(TBMABDC)存在下,过氧化二硫酸钾(PDS)作为水溶性引发剂的甲基丙烯酸正丁酯(n-BMA)自由基聚合的动力学和机理。研究了多位相转移催化剂(MPTC)。聚合反应是在无氧,无搅拌的条件下于60°±1°C的恒定温度在环己烷-水两相系统中进行的。确定了聚合速率(Rp)对单体,引发剂和催化剂浓度,水相体积分数,溶剂极性和温度的依赖性。发现关于单体,引发剂和多位相转移催化剂的反应顺序分别为0.50、1.0和0.52。根据实验结果,提出了合适的反应机理,并对其意义进行了探讨。制备的聚合物通过光谱分析进行表征。

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