Kinetic study on the one-pot synthesis of dimethyl carbonate in supercritical CO2 conditions

被引:34
作者
Cui, H
Wang, T [1 ]
Wang, FJ
Gu, CR
Wang, PL
Dai, YY
机构
[1] Tsinghua Univ, Dept Chem Engn, State Key Lab Chem Engn, Beijing 100084, Peoples R China
[2] Shandong Univ Technol, Coll Chem Engn, Zibo 255049, Peoples R China
[3] Shanghai Petrochem Co Ltd, SINOPEC, Shanghai 200540, Peoples R China
关键词
D O I
10.1021/ie049715r
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The kinetics of one-pot synthesis of dimethyl carbonate (DMC) was investigated using ethylene epoxide (EO), methanol, and CO2 as raw materials and a mixture of KI and K2CO3 as a catalyst under supercritical CO2 conditions. The reaction pathway of the one-pot process is that EO first reacts with CO2 to form ethylene carbonate (EC) and then EC reacts with methanol to produce DMC and ethylene glycol (EG). EC formation is a relatively fast reaction, whereas the transesterification of EC with methanol to form DMC is a relatively slow reaction and the rate-control step of the one-pot synthesis. 2-Methoxyethanol (ME), which is the exclusive byproduct, is predominantly formed by the reaction of EC with methanol. An isothermal kinetics model and an isobaric kinetics model for the one-pot synthesis of DMC were developed. The relative standard deviations of the models from the experiment data were less than +/-15% and +/-10%, respectively. The effects of temperature and CO2 density on the reaction rates and selectivity were discussed.
引用
收藏
页码:7732 / 7739
页数:8
相关论文
共 29 条
  • [1] ABRAMS E, 1979, OTHMER ENCY CHEM TEC
  • [2] Aresta M, 1997, CHEMTECH, V27, P32
  • [3] Concurrent synthesis of dimethyl carbonate and ethylene glycol via transesterification of ethylene carbonate and methanol using smectite catalysts containing Mg and/or Ni
    Bhanage, BM
    Fujita, S
    He, YF
    Ikushima, Y
    Shirai, M
    Torii, K
    Arai, M
    [J]. CATALYSIS LETTERS, 2002, 83 (3-4) : 137 - 141
  • [4] Synthesis of dimethyl carbonate and glycols from carbon dioxide, epoxides, and methanol using heterogeneous basic metal oxide catalysts with high activity and selectivity
    Bhanage, BM
    Fujita, S
    Ikushima, Y
    Arai, M
    [J]. APPLIED CATALYSIS A-GENERAL, 2001, 219 (1-2) : 259 - 266
  • [5] Buysch H.-J, 1980, Patent No. [US 4181676, 4181676]
  • [6] Reaction of dialkyltin methoxide with carbon dioxide relevant to the mechanism of catalytic carbonate synthesis
    Choi, JC
    Sakakura, T
    Sako, T
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (15) : 3793 - 3794
  • [7] Transesterification of ethylene carbonate with methanol in supercritical carbon dioxide
    Cui, HY
    Wang, T
    Wang, FJ
    Gu, CR
    Wang, PL
    Dai, YY
    [J]. JOURNAL OF SUPERCRITICAL FLUIDS, 2004, 30 (01) : 63 - 69
  • [8] One-pot synthesis of dimethyl carbonate using ethylene oxide, methanol, and carbon dioxide under supercritical conditions
    Cui, HY
    Wang, T
    Wang, FJ
    Gu, CR
    Wang, PL
    Dai, YY
    [J]. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2003, 42 (17) : 3865 - 3870
  • [9] Synthesis of dimethyl carbonate by vapor phase oxidative carbonylation of methanol over Cu-based catalysts
    Han, MS
    Lee, BG
    Suh, I
    Kim, HS
    Ahn, BS
    Hong, SI
    [J]. JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2001, 170 (1-2) : 225 - 234
  • [10] Kinetics of dimethyl carbonate synthesis from ethylene carbonate and methanol using alkalimetal compounds as catalysts
    Han, MS
    Lee, BG
    Ahn, BS
    Park, KY
    Hong, SI
    [J]. REACTION KINETICS AND CATALYSIS LETTERS, 2001, 73 (01): : 33 - 38