Synthesis of C2+ hydrocarbons by CO2 hydrogenation over the composite catalyst of Cu-Zn-Al oxide and HB zeolite using two-stage reactor system under low pressure

被引:38
作者
Fujiwara, Masahiro [1 ]
Sakurai, Hiroaki [1 ]
Shiokawa, Kumi [1 ]
Iizuka, Yasuo [1 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Kansai Ctr, Ikeda, Osaka 5638577, Japan
基金
日本科学技术振兴机构;
关键词
CO2; hydrogenation; C2+ hydrocarbons; Methanol synthesis; MTG reaction; Composite catalyst; Two-stage reactor system; CARBON-DIOXIDE HYDROGENATION; METHANOL SYNTHESIS CATALYST; WATER-GAS-SHIFT; HYBRID CATALYSTS; SELECTIVE SYNTHESIS; CONVERSION; ENERGY; DECOMPOSITION; BEHAVIOR; FUELS;
D O I
10.1016/j.cattod.2014.04.032
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The combination of methanol synthesis and methanol-to-gasoline (MTG) reaction is a beneficial process to produce particular C2+ hydrocarbons from CO2 and H-2, because MTG reaction can produce C2+ hydrocarbons selectively without the formation of methane. However, the composite catalysts consisting of methanol synthesis catalyst and zeolite previously reported have produced C2+ hydrocarbons in poor yields especially under low pressure conditions. This paper reports the high yield production of C2+ hydrocarbons by CO2 hydrogenation using a two-stage reaction system consisting of a Cu-Zn-Al oxide catalyst in the first reactor and a composite catalyst of the Cu-Zn-Al oxide and HB (zeolite beta) in the second reactor. The key points of this system are reversed water-gas-shift (RWGS) reaction in the first reactor and the following H2O removal before the second reactor. The gas mixture supplied to the second reactor containing much amount of CO and little H2O enhanced the methanol synthesis and suppressed the methanol decomposition to CO over the Cu-Zn-Al oxide catalyst in the composite catalyst, promoting the MTG reaction to produce C2+ hydrocarbons over HB zeolite. The highest yield of C2+ hydrocarbons reached to approximately 15 C-mol% under 0.98 MPa. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:255 / 260
页数:6
相关论文
共 37 条
[1]   Hydrocarbon synthesis from CO2 over Fe-Cu catalysts [J].
Ando, H ;
Xu, Q ;
Fujiwara, M ;
Matsumura, Y ;
Tanaka, M ;
Souma, Y .
CATALYSIS TODAY, 1998, 45 (1-4) :229-234
[2]   Study on the carbon dioxide hydrogenation to iso-alkanes over Fe-Zn-M/zeolite composite catalysts [J].
Bai, RX ;
Tan, YS ;
Han, YZ .
FUEL PROCESSING TECHNOLOGY, 2004, 86 (03) :293-301
[3]   Catalysis for CO2 conversion: a key technology for rapid introduction of renewable energy in the value chain of chemical industries [J].
Centi, Gabriele ;
Quadrelli, Elsje Alessandra ;
Perathoner, Siglinda .
ENERGY & ENVIRONMENTAL SCIENCE, 2013, 6 (06) :1711-1731
[4]   Development of methanol decomposition catalysts for production of H2 and CO [J].
Cheng, WH .
ACCOUNTS OF CHEMICAL RESEARCH, 1999, 32 (08) :685-691
[5]   CO2 capture via catalytic hydrogenation to methanol: Thermodynamic limit vs. 'kinetic limit' [J].
Fornero, Esteban L. ;
Chiavassa, Dante L. ;
Bonivardi, Adrian L. ;
Baltanas, Miguel A. .
CATALYSIS TODAY, 2011, 172 (01) :158-165
[6]   SELECTIVE SYNTHESIS OF C2-C5 HYDROCARBONS FROM CARBON-DIOXIDE UTILIZING A HYBRID CATALYST COMPOSED OF A METHANOL SYNTHESIS CATALYST AND ZEOLITE [J].
FUJIMOTO, K ;
SHIKADA, T .
APPLIED CATALYSIS, 1987, 31 (01) :13-23
[7]   HYDROCARBON SYNTHESIS FROM CARBON-DIOXIDE AND HYDROGEN OVER CU-ZN-CR OXIDE ZEOLITE HYBRID CATALYSTS [J].
FUJIWARA, M ;
SOUMA, Y .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1992, (10) :767-768
[8]   HYDROGENATION OF CARBON-DIOXIDE OVER CU-ZN-CHROMATE/ZEOLITE COMPOSITE CATALYST - THE EFFECTS OF REACTION BEHAVIOR OF ALKENES ON HYDROCARBON SYNTHESIS [J].
FUJIWARA, M ;
ANDO, H ;
TANAKA, M ;
SOUMA, Y .
APPLIED CATALYSIS A-GENERAL, 1995, 130 (01) :105-116
[9]   HYDROGENATION OF CARBON-DIOXIDE OVER CU-ZN-CR OXIDE CATALYSTS [J].
FUJIWARA, M ;
ANDO, H ;
TANAKA, M ;
SOUMA, Y .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1994, 67 (02) :546-550
[10]   HYDROGENATION OF CARBON-DIOXIDE OVER FE-ZNO/ZEOLITE COMPOSITE CATALYSTS [J].
FUJIWARA, M ;
ANDO, H ;
MATSUMOTO, M ;
MATSUMURA, Y ;
TANAKA, M ;
SOUMA, Y .
CHEMISTRY LETTERS, 1995, (09) :839-840