{"title":"均相催化醋酸与nopol酯化合成nopyl乙酸的动力学","authors":"Aída Luz Villa-Holguín, Eliana Paola Hurtado-Burbano","doi":"10.17533/UDEA.REDIN.N89A03","DOIUrl":null,"url":null,"abstract":"The esterification of nopol with acetic acid to produce nopyl acetate using sulfuric acid as homogeneous catalyst was studied. The reactions were carried out in a batch reactor, at different temperatures (50, 60, 70 and 80 °C), catalyst concentrations (0.0184, 0.0275, 0.0367 and 0.0480 mol L -1 ) and molar ratio of acetic acid to nopol (1: 1, 1:2, 1:3 and 1: 4); the chemical equilibrium composition was measured at those reaction conditions. It was found that the equilibrium composition is a weak function of temperature, equilibrium conversion was 63, 68, 71 and 75% at 50, 60, 70 and 80°C, respectively. The reaction was described with a simple power-law model with a second-order kinetic model for both the forward and the backward reaction, using concentration and activities which were predicted by the Universal Functional group Contribution (UNIFAC) method for considering non-ideal behavior of the liquid phase. The forward reaction rate and the equilibrium constants increased with temperature; the relation of the pre-exponential factor with the catalyst amount was evaluated. The activation energy and pre-exponential factor estimated for the forward reaction using the kinetic model based on concentration, were respectively, 28.08 kJ mol -1 and 11126 L mol -1 h -1 with a concentration of catalyst of 0.0275 M. Using the kinetic model based on activities, the forward reaction rate constant was 28.56 kJ·mol -1 and the k fo,act was 33860 L mol -1 h -1 . The enthalpy (34.90 kJ mol -1 ) and the entropy (0.12 kJ mol -1 K -1 ) of reaction were determined using van’t Hoff equation.","PeriodicalId":21428,"journal":{"name":"Revista Facultad De Ingenieria-universidad De Antioquia","volume":null,"pages":null},"PeriodicalIF":0.9000,"publicationDate":"2018-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Kinetics of nopyl acetate synthesis by homogeneously catalyzed esterification of acetic acid with nopol\",\"authors\":\"Aída Luz Villa-Holguín, Eliana Paola Hurtado-Burbano\",\"doi\":\"10.17533/UDEA.REDIN.N89A03\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The esterification of nopol with acetic acid to produce nopyl acetate using sulfuric acid as homogeneous catalyst was studied. 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引用次数: 1
摘要
以硫酸为均相催化剂,研究了nopol与乙酸的酯化反应制醋酸nopyl。在间歇反应器中,在不同温度(50、60、70和80℃)、催化剂浓度(0.0184、0.0275、0.0367和0.0480 mol L -1)和乙酸与nopol的摩尔比(1:1、1:2、1:3和1:4)下进行反应;测定了反应条件下的化学平衡组成。结果表明,在50、60、70、80℃的温度下,平衡组分的转化率分别为63、68、71、75%。用一个简单的幂律模型来描述该反应,该反应的正反应和反反应都有一个二级动力学模型,考虑到液相的非理想行为,使用通用官能团贡献(UNIFAC)方法预测的浓度和活度。正反应速率和平衡常数随温度升高而增大;考察了指前因子与催化剂用量的关系。在催化剂浓度为0.0275 m的条件下,基于浓度的动力学模型计算得到正向反应的活化能为28.08 kJ mol -1,指前因子为11126 L mol -1 h -1,反应速率常数为28.56 kJ·mol -1,反应k为33860 L mol -1 h -1。用范霍夫方程计算了反应焓(34.90 kJ mol -1)和熵(0.12 kJ mol -1 K -1)。
Kinetics of nopyl acetate synthesis by homogeneously catalyzed esterification of acetic acid with nopol
The esterification of nopol with acetic acid to produce nopyl acetate using sulfuric acid as homogeneous catalyst was studied. The reactions were carried out in a batch reactor, at different temperatures (50, 60, 70 and 80 °C), catalyst concentrations (0.0184, 0.0275, 0.0367 and 0.0480 mol L -1 ) and molar ratio of acetic acid to nopol (1: 1, 1:2, 1:3 and 1: 4); the chemical equilibrium composition was measured at those reaction conditions. It was found that the equilibrium composition is a weak function of temperature, equilibrium conversion was 63, 68, 71 and 75% at 50, 60, 70 and 80°C, respectively. The reaction was described with a simple power-law model with a second-order kinetic model for both the forward and the backward reaction, using concentration and activities which were predicted by the Universal Functional group Contribution (UNIFAC) method for considering non-ideal behavior of the liquid phase. The forward reaction rate and the equilibrium constants increased with temperature; the relation of the pre-exponential factor with the catalyst amount was evaluated. The activation energy and pre-exponential factor estimated for the forward reaction using the kinetic model based on concentration, were respectively, 28.08 kJ mol -1 and 11126 L mol -1 h -1 with a concentration of catalyst of 0.0275 M. Using the kinetic model based on activities, the forward reaction rate constant was 28.56 kJ·mol -1 and the k fo,act was 33860 L mol -1 h -1 . The enthalpy (34.90 kJ mol -1 ) and the entropy (0.12 kJ mol -1 K -1 ) of reaction were determined using van’t Hoff equation.
期刊介绍:
Revista Facultad de Ingenieria started in 1984 and is a publication of the School of Engineering at the University of Antioquia.
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