Carbon deposition and catalytic deactivation during CO2 reforming of CH4 over Co/γ-Al2O3 catalysts

被引:278
作者
Ruckenstein, E [1 ]
Wang, HY [1 ]
机构
[1] SUNY Buffalo, Dept Chem Engn, Amherst, NY 14260 USA
关键词
carbon dioxide reforming of methane; synthesis gas; Co catalyst; deactivation;
D O I
10.1006/jcat.2001.3458
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 reaction behavior and carbon deposition during the CO2/CH4 reforming reaction have been investigated over the gamma-Al2O3-supported Co catalysts as a function of Co loading (between 2 and 20 wt%) and calcination temperature (T-c = 500 or 1000degreesC). It was found that the stability of Co/gamma-Al2O3 catalysts was strongly dependent on the Co loading and calcination temperature. For some loadings (6 wt% for T-c = 500degreesC and 9 wt% for T-c = 1000degreesC), stable activities have been achieved. However, over the catalysts with high Co loadings (>12 wt%), notable amounts of carbon were accumulated during reforming, and deactivation was observed. Moreover, severe deactivation was also noted over the 2 wt% catalysts, both when carbon deposition occurred (T-c = 500degreesC) or was absent (T-c = 1000degreesC). In the latter case, the oxidation of the metallic sites was responsible for the deactivation. Hence, there are two different deactivation mechanisms, namely, carbon deposition and oxidation of metallic sites. The activities were stable when a balance between carbon formation and its oxidation could be achieved. (C) 2002 Elsevier Science.
引用
收藏
页码:289 / 293
页数:5
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共 39 条
[21]  
Rostrup-Nielsen J.R., 1984, CATAL SCI TECHNOL, V5, P1, DOI [DOI 10.1007/978-3-642-93247-2_, DOI 10.1007/978-3-642-93247-2_1]
[22]   CO2-REFORMING OF METHANE OVER TRANSITION-METALS [J].
ROSTRUPNIELSEN, JR ;
HANSEN, JHB .
JOURNAL OF CATALYSIS, 1993, 144 (01) :38-49
[23]   Carbon dioxide reforming of methane to synthesis gas over supported cobalt catalysts [J].
Ruckenstein, E ;
Wang, HY .
APPLIED CATALYSIS A-GENERAL, 2000, 204 (02) :257-263
[24]   The effect of precursor and preparation conditions of MgO on the CO2 reforming of CH4 over NiO/MgO catalysts [J].
Ruckenstein, E ;
Hu, YH .
APPLIED CATALYSIS A-GENERAL, 1997, 154 (1-2) :185-205
[25]   Carbon dioxide reforming of methane over nickel alkaline earth metal oxide catalysts [J].
Ruckenstein, E ;
Hu, YH .
APPLIED CATALYSIS A-GENERAL, 1995, 133 (01) :149-161
[26]   CATALYTIC REACTION OF CH4 WITH CO-2 OVER ALUMINA-SUPPORTED PT METALS [J].
SOLYMOSI, F ;
KUTSAN, G ;
ERDOHELYI, A .
CATALYSIS LETTERS, 1991, 11 (02) :149-156
[27]   Effect of promotion with Sn on supported Pt catalysts for CO2 reforming of CH4 [J].
Stagg, SM ;
Romeo, E ;
Padro, C ;
Resasco, DE .
JOURNAL OF CATALYSIS, 1998, 178 (01) :137-145
[28]   Studies on carbon deposition in CO2 reforming of CH4 over nickel-magnesia solid solution catalysts [J].
Tomishige, K ;
Chen, YG ;
Fujimoto, K .
JOURNAL OF CATALYSIS, 1999, 181 (01) :91-103
[29]   FORMATION AND REMOVAL OF COKE FROM NICKEL-CATALYST [J].
TRIMM, DL .
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 1977, 16 (02) :155-189
[30]   Carbon dioxide reforming of methane to synthesis gas over supported rhodium catalysts: the effect of support [J].
Wang, HY ;
Ruckenstein, E .
APPLIED CATALYSIS A-GENERAL, 2000, 204 (01) :143-152