首页> 外文期刊>European Journal of Lipid Science and Technology >Optimization of epoxidation of ricinoleic acid methyl ester by hydrogen peroxide and phase-transfer catalyst using response surface methodology
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Optimization of epoxidation of ricinoleic acid methyl ester by hydrogen peroxide and phase-transfer catalyst using response surface methodology

机译:利用响应面法测定过氧化氢和相转移催化剂的氯氰酸甲酯环氧化的优化

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摘要

The epoxidation of ricinoleic acid methyl ester (RAME) has been investigated using an environmentally friendly oxidant (i.e., hydrogen peroxide) and a phase-transfer catalyst ([-C5H5N(CH2)(15)CH3](3)[PW4O16]) in dichloroethane. The response surface methodology (RSM), based on the Box-Behnken design was used to assess individual and interactive effects of the process variables and to optimize the epoxidation reaction condition. The coefficient of determination (R-2=0.9544) obtained from analysis of the variance confirmed the suitability of the fitted model. The RSM analysis results indicated that the molar ratio of H2O2 to CC bonds and the reaction temperature are the most significant (P0.01) factors affecting the conversion of RAME epoxide. In addition, the interaction between the H2O2/CC molar ratio and the catalyst dosage also has significant effect (P0.05) on the conversion of RAME epoxide. The optimum reaction conditions for the epoxidation of RAME were H2O2: CC molar ratio of 1.93:1, catalyst dosage of 3.11wt% (substrate:catalyst molar ratio=207), reaction temperature of 52 degrees C, and reaction time of 75min, under which a conversion of 94.52% could be achieved. The epoxidation of RAME by hydrogen peroxide and the (-C5H5N[CH2](15)CH3)(3)(PW4O16) phase-transfer catalyst followed pseudo-first order kinetics with an activation energy (E-a) of approximately 21.6kJ/mol. The reaction process is a mass-transfer control process.
机译:使用环保型氧化剂(即,过氧化氢)和相转移催化剂([-C5H5N(CH2)(15)CH3](3)[PW4O16])研究了蓖麻油酸甲酯(rame)的环氧化。二氯乙烷。基于Box-Behnken设计的响应面方法(RSM)用于评估过程变量的个体和交互式效果,并优化环氧化反应条件。根据方差分析获得的测定系数(R-2 = 0.9544)证实了拟合模型的适用性。 RSM分析结果表明,H 2 O 2至CC键的摩尔比和反应温度是影响荷氧化物转化的最显着(P <0.01)因素。此外,H 2 O 2 / CC摩尔比和催化剂剂量之间的相互作用也具有显着的效果(P <0.05)。 rame环氧化的最佳反应条件为H 2 O 2:CC摩尔比为1.93:1,催化剂剂量为3.11wt%(基材:催化剂摩尔比= 207),反应温度为52℃,反应时间为75min可以实现94.52%的转换。通过过氧化氢的丙肟和(-C5H5N [CH2](15)CH 3)(3)(PW4O16)相转移催化剂的氨氧化术后伪第一阶动力学,其活化能量(E-A)约为21.6kJ / mol。反应过程是传质控制过程。

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