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Multi-site phase transfer catalyzed radical polymerization of methyl methacrylate in mixed aqueous–organic medium: a kinetic study

机译:混合水性有机培养基中甲基丙烯酸甲酯的多位相转移催化自由基聚合:动力学研究

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This work establishes the kinetics of radical polymerization of methyl methacrylate in an aqueous–organic two-phase system using 1,4-bis (triethylmethylammonium) benzene dichloride (TEMABDC) as multi-site phase transfer catalyst and potassium peroxydisulphate (K2S2O8) as water-soluble initiator at 60?±?1?°C under nitrogen atmosphere. The role of concentrations of monomer, initiator, catalyst, acid and ionic strength, temperature and volume fraction of aqueous phase on the rate of polymerization (Rp) was investigated. The rate of polymerization (Rp); Rp α [MMA]0.64, [TEMABDC]1.24 and [K2S2O8]1.50. The rate of polymerization increases with an increase in the concentration of monomer, initiator, catalyst and temperature. A generalized reaction model was developed to explain the phase transfer catalyzed polymerization reaction. Based on the kinetic results, radical mechanism has been derived. The activation energy and other thermodynamic parameters were calculated. The FT-IR spectroscopy validates a band of 1732?cm?1 of ester group of the obtained polymer. The viscosity average molecular weight of the PMMA was found 1.6955?×?104?g/mol.
机译:这项工作建立了使用1,4-双(三乙基甲基铵)苯二氯(TemaBDC)作为多位相转移催化剂和过氧氢硫酸钾(K2S2O8)作为水 - 甲基丙烯酸甲酯在水性有机两相体系中甲基丙烯酸甲酯的激进聚合动力学。在氮气氛下,可溶性引发剂在60?±1?°C下。研究了单体,引发剂,催化剂,酸和离子强度,水相对聚合速率(RP)的作用。聚合速率(RP); RPα[MMA] 0.64,[TemaBDC] 1.24和[K2S2O8] 1.50。聚合速率随着单体,引发剂,催化剂和温度的浓度而增加。开发了广义反应模型以解释相转移催化的聚合反应。基于动力学结果,已经推导出基于动力学机制。计算激活能量和其他热力学参数。 FT-IR光谱验证所得聚合物的酯基的1732Ω·cm 2的条带。发现PMMA的粘度平均分子量为1.6955?×104?G / mol。

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