Kinetic study for the direct synthesis of dimethyl carbonate from methanol and CO2 over CeO2 at high pressure conditions

被引:78
作者
Santos, B. A. V. [1 ]
Pereira, C. S. M. [1 ]
Silva, V. M. T. M. [1 ]
Loureiro, J. M. [1 ]
Rodrigues, A. E. [1 ]
机构
[1] Univ Porto, Fac Engn, Dept Chem Engn, Lab Separat & React Engn, P-4200465 Oporto, Portugal
关键词
Dimethyl carbonate; High pressure reaction; CeO2; ORGANIC CARBONATES; ZIRCONIA CATALYSTS; DIOXIDE; TRANSESTERIFICATION; CONVERSION; ROUTE; ACID;
D O I
10.1016/j.apcata.2013.02.003
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The kinetics for the direct synthesis of dimethyl carbonate was studied over CeO2 at high pressure conditions in a batch reactor. Langmuir-Hinshelwood and Eley-Rideal mechanisms were proposed and compared by the performance of the respective reaction rate expression in fitting to the experimental kinetic data. The reactions were held at different temperatures (378-408 K), CO2/methanol molar ratios (1.1-4.0) and pressures (15-20 MPa) in order to adjust the kinetic parameters. An activation energy of 106 kJ mol(-1), as well as the standard enthalpy and Gibbs energy of reaction (-20.10 and 31.50 kJ mol(-1)) were calculated from experiments. Furthermore, the changes in pressure revealed an effect on the kinetic constant, with an activation volume equal to -0.208 cm(3) mol(-1). (c) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:219 / 226
页数:8
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