Ethylbenzene Dehydrogenation in the Presence of CO2 over MCF-Supported Vanadium Oxide Catalysts

被引:18
作者
Li Chunguang [1 ]
Miao Changxi [2 ]
Nie Yingying [1 ]
Yue Yinghong [1 ]
Gu Songyuan [2 ]
Yang Weimin [2 ]
Hua Weiming [1 ]
Gao Zi [1 ]
机构
[1] Fudan Univ, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China
[2] SINOPEC, Shanghai Res Inst Petrochem Technol, Shanghai 201208, Peoples R China
基金
中国国家自然科学基金;
关键词
vanadia; mesocellular silica foam; supported catalyst; ethylbenzene dehydrogenation; styrene; carbon dioxide; CARBON-DIOXIDE; OXIDATIVE DEHYDROGENATION; SILICA FOAMS; STYRENE; PERFORMANCE;
D O I
10.1016/S1872-2067(10)60099-X
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A series of vanadia catalysts supported on mesocellular silica foam (MCF) with a V content ranging from 2% to 10% were studied with respect to their performance in the dehydrogenation of ethylbenzene (EB) to styrene in the presence of CO2 The structural and textural characterization of these catalysts was done using N-2 adsorption, X-ray diffraction, and temperature-programmed reduction These catalysts were found to be effective for the dehydrogenation reaction and the 6%V/MCF catalyst showed the highest activity The MCF-supported vanadia catalysts exhibited far higher activity than their conventional V/MCM-41 counterparts, which can be attributed to the higher reducibility and better diffusion of reactants and products in the former catalysts A higher conversion was obtained during EB dehydrogenation with CO2 than with N-2 This is due to the oxidative dehydrogenation of EB with the help of oxygen that originates from CO2 as well as the coupling of EB simple dehydrogenation with the reverse water-gas shift reaction
引用
收藏
页码:993 / 998
页数:6
相关论文
共 29 条
  • [1] Oxidative dehydrogenation of ethylbenzene with carbon dioxide on alkali-promoted Fe active carbon catalysts
    Badstube, T
    Papp, H
    Kustrowski, P
    Dziembaj, R
    [J]. CATALYSIS LETTERS, 1998, 55 (3-4) : 169 - 172
  • [2] An overview on the dehydrogenation of alkylbenzenes with carbon dioxide over supported vanadium-antimony oxide catalysts
    Chang, Jong-San
    Hong, Do-Young
    Vislovskiy, Vladislav P.
    Park, Sang-Eon
    [J]. CATALYSIS SURVEYS FROM ASIA, 2007, 11 (1-2) : 59 - 69
  • [3] Utilization of carbon dioxide as soft oxidant in the dehydrogenation of ethylbenzene over supported vanadium-antimony oxide catalystst
    Chang, JS
    Vislovskiy, VP
    Park, MS
    Hong, DY
    Yoo, JS
    Park, SE
    [J]. GREEN CHEMISTRY, 2003, 5 (05) : 587 - 590
  • [4] Chen GL, 2009, CHINESE J CATAL, V30, P619
  • [5] Effects of Li Promoter on the Catalytic Performance of Fe-Li/AC for Ethylbenzene Dehydrogenation in the Presence of CO2
    Chen Shuwei
    Qin Zhangfeng
    Sun Ailing
    Wang Jianguo
    [J]. CHINESE JOURNAL OF CATALYSIS, 2009, 30 (04) : 359 - 364
  • [6] Structure and properties of the alumina-supported vanadia catalysts for ethylbenzene dehydrogenation in the presence of carbon dioxide
    Chen, SW
    Qin, ZF
    Xu, XF
    Wang, JG
    [J]. APPLIED CATALYSIS A-GENERAL, 2006, 302 (02) : 185 - 192
  • [7] Preparation of highly active Cr2O3-SiO2 catalyst by sol-gel method for ethylbenzene dehydrogenation in the presence of CO2
    Li, HY
    Yue, YH
    Miao, CX
    Xie, ZK
    Hua, WM
    Gao, Z
    [J]. CHINESE JOURNAL OF CATALYSIS, 2006, 27 (01) : 4 - 6
  • [8] Effects of VOx/AlMCM-41 Surface Structure on Ethylbenzene Oxydehydrogenation in the Presence of CO2
    Li, Zhenhuan
    Su, Kunmei
    Cheng, Bowen
    Shen, Dexin
    Zhou, Yu
    [J]. CATALYSIS LETTERS, 2010, 135 (1-2) : 135 - 140
  • [9] Preparation and high performance of La2O3-V2O5/MCM-41 catalysts for ethylbenzene dehydrogenation in the presence of CO2
    Liu, B. S.
    Chang, R. Z.
    Jiang, L.
    Liu, W.
    Au, C. T.
    [J]. JOURNAL OF PHYSICAL CHEMISTRY C, 2008, 112 (39) : 15490 - 15501
  • [10] Dehydrogenation of ethylbenzene to styrene over LaVOx/SBA-15 catalysts in the presence of carbon dioxide
    Liu, B. S.
    Rui, G.
    Chang, R. Z.
    Au, C. T.
    [J]. APPLIED CATALYSIS A-GENERAL, 2008, 335 (01) : 88 - 94