Catalytic Conversion of Cyclopentanone into Dimethyl Adipate over Solid Basic Catalysts with Dimethyl Carbonate

被引:0
|
作者
Martinez-Salazar, Irene [1 ]
Orozco-Saumell, Ana [1 ]
Lopez Granados, Manuel [1 ]
Mariscal, Rafael [1 ]
机构
[1] Inst Catalysis & Petrochem ICP CSIC, EQS Grp, Sustainable Energy & Chem Grp, C Marie Curie 2, Madrid 28049, Spain
关键词
cyclopentanone; dimethyl carbonate; dimethyl adipate; solid basic catalysts; ADIPIC ACID; TRANSFORMATION; CARBONYLATION; CHEMISTRY; BIOMASS;
D O I
10.3390/catal14010086
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 synthesis of dimethyl adipate (DAP), a stable configuration of adipic acid, from biomass-derived cyclopentanone (CPO) and dimethyl carbonate (DMC) constitutes an attractive greener route than petroleum-based industrial processes. Solid basic catalysts such as MgO, Mg5(CO3)4(OH)2 center dot 4H2O, KOCH3 and Ca(OCH3)2 have been used achieving a DAP yield up to 30% at 533 K. In addition to the type of catalyst, other operating conditions such as the substrate, reaction time, temperature and CPO concentration have been studied. The methylation of DAP and CPO and the self-aldol condensation of CPO to form dimers and oligomers are reactions that occur in parallel with the production of DAP. It has been established that the main challenge is the self-aldol condensation of CPO. It has been identified that at short reaction times, to prevent methylation, and at dilute concentrations, to avoid CPO self-condensation, the DAP formation rate is much higher than these other competitive reactions. Finally, it should be noted that a DAP productivity up to 3.45 g center dot gcat-1 center dot h-1 has been achieved under mild conditions.
引用
收藏
页数:12
相关论文
共 50 条
  • [41] A new process for the synthesis of diphenyl carbonate from dimethyl carbonate and phenol over heterogeneous catalysts
    Kim, WB
    Lee, JS
    CATALYSIS LETTERS, 1999, 59 (01) : 83 - 88
  • [42] Dimethyl carbonate synthesis over solid base catalysts derived from Ca–Al layered double hydroxides
    Yunhui Liao
    Feng Li
    Xin Dai
    Ning Zhao
    Fukui Xiao
    Chemical Papers, 2018, 72 : 1963 - 1971
  • [43] Catalytic conversion of chloromethane to methanol and dimethyl ether over mesoporous γ-alumina
    Khaleel, Abbas
    Shehadi, Ihsan
    Al-Marzouqi, Ali
    FUEL PROCESSING TECHNOLOGY, 2011, 92 (09) : 1783 - 1789
  • [44] Synthesis of glycerol carbonate by transesterification of glycerol with dimethyl carbonate over MgAl mixed oxide catalysts
    Liu, Peng
    Derchi, Margherita
    Hensen, Emiel J. M.
    APPLIED CATALYSIS A-GENERAL, 2013, 467 : 124 - 131
  • [45] A new process for the synthesis of diphenyl carbonate from dimethyl carbonate and phenol over heterogeneous catalysts
    Won Bae Kim
    Jae Sung Lee
    Catalysis Letters, 1999, 59 : 83 - 88
  • [46] Synthesis of glycerol carbonate by transesterification of glycerol with dimethyl carbonate over Mg/Al/Zr catalysts
    Malyaadri, M.
    Jagadeeswaraiah, K.
    Prasad, P. S. Sai
    Lingaiah, N.
    APPLIED CATALYSIS A-GENERAL, 2011, 401 (1-2) : 153 - 157
  • [47] Synthesis of dimethyl carbonate from urea and methanol over metal oxide catalysts
    Zhao, Xin-Qiang
    Wang, Yan-Ji
    Shen, Qun-Bing
    Yang, Hong-Jian
    Zhang, Ji-Yan
    Shiyou Xuebao, Shiyou Jiagong/Acta Petrolei Sinica (Petroleum Processing Section), 2002, 18 (05): : 47 - 52
  • [48] Trichloroethylene catalytic conversion over acidic solid catalysts
    Finocchio, E
    Sapienza, G
    Baldi, M
    Busca, G
    APPLIED CATALYSIS B-ENVIRONMENTAL, 2004, 51 (03) : 143 - 148
  • [49] Transesterification of Ethylene Carbonate with Dimethyl Terephthalate over Various Metal Acetate Catalysts
    ZHANG Dan1
    2. Graduate School of Chinese Academy of Sciences
    Chemical Research in Chinese Universities, 2007, (02) : 173 - 175
  • [50] Transesterification of ethylene carbonate with dimethyl terephthalate over various metal acetate catalysts
    Zhang Dan
    Jia Shu-yong
    Wang Yue
    Yao Jie
    Wang Gong-ying
    CHEMICAL RESEARCH IN CHINESE UNIVERSITIES, 2007, 23 (02) : 173 - 175