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Modelling of a pervaporation membrane reactor during esterification reaction coupled with separation to produce ethyl acetate

机译:酯化反应过程中全蒸发膜反应器的建模与分离以生成乙酸乙酯

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As a follow up to the previous report on the experimental study of esterification reaction to yield ethyl acetate in a pervaporation membrane reactor (PMR), in this study; modelling of PMR during esterification reaction coupled with separation is presented. The analyzed system is the esterification reaction catalysed by sulfuric acid and Amberlyst 15 in a batch PMR in the temperature range of 50-70℃ using polydimethylsiloxane (PDMS) membranes permselective to ethyl acetate. In this way, conversions were increased by continuous removal of ethyl acetate from the reaction medium.The theoretical model was developed taking account permeation of the all components in the reaction mixture. The kinetic calculations were made on the assumptions that the reaction obeyed second order kinetics. The model satisfactorily agrees with the experimental results obtained in the previous work, thus allowing the prediction of the conversion variation with the pervaporation time. The coefficient of determination, R2, was in the range of 0.9798 to 0.9991. This modelling methodology could be used to extrapolate or to scale-up this type of systems as it provides assistance to analyze the effect of the operating parameters on the conversions during the esterification process.
机译:作为先前关于在全蒸发膜反应器(PMR)中进行酯化反应生成乙酸乙酯的实验研究的报告的后续研究;提出了酯化反应与分离过程中PMR的数学模型。所分析的系统是在50-70℃的温度范围内,使用选择性渗透乙酸乙酯的聚二甲基硅氧烷(PDMS)膜,在分批PMR中,由硫酸和Amberlyst 15催化的酯化反应。以此方式,通过从反应介质中连续除去乙酸乙酯来提高转化率。建立了考虑反应混合物中所有组分渗透的理论模型。动力学计算是在反应遵循二级动力学的假设下进行的。该模型与先前工作中获得的实验结果令人满意地吻合,因此可以预测转化率随全蒸发时间的变化。测定系数R2在0.9798至0.9991的范围内。这种建模方法可用于推断或扩大此类系统的规模,因为它有助于分析酯化过程中操作参数对转化率的影响。

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