Selective catalytic reduction of NO by hydrocarbons on Ga2O3/Al2O3 catalysts
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Shimizu, K
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Nagoya Univ, Grad Sch Engn, Dept Appl Chem, Chikusa Ku, Nagoya, Aichi 46401, JapanNagoya Univ, Grad Sch Engn, Dept Appl Chem, Chikusa Ku, Nagoya, Aichi 46401, Japan
Shimizu, K
[1
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Satsuma, A
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Nagoya Univ, Grad Sch Engn, Dept Appl Chem, Chikusa Ku, Nagoya, Aichi 46401, JapanNagoya Univ, Grad Sch Engn, Dept Appl Chem, Chikusa Ku, Nagoya, Aichi 46401, Japan
Satsuma, A
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Hattori, T
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Nagoya Univ, Grad Sch Engn, Dept Appl Chem, Chikusa Ku, Nagoya, Aichi 46401, JapanNagoya Univ, Grad Sch Engn, Dept Appl Chem, Chikusa Ku, Nagoya, Aichi 46401, Japan
Hattori, T
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[1] Nagoya Univ, Grad Sch Engn, Dept Appl Chem, Chikusa Ku, Nagoya, Aichi 46401, Japan
Catalytic properties of supported gallium oxides have been examined for the selective reduction of NO by CH4 in excess oxygen. The activity was greatly affected by the support; Ga2O3/Al2O3 (Al2O3 supported Ga2O3) and Ga2O3-Al2O3 mixed oxide exhibited high activity and selectivity as comparable to Ga-ZSM-5, while unsupported Ga2O3 and the other supported Ga2O3 were ineffective. For Ga2O3/Al2O3, the activity changed with Ga2O3 content, and was highest at about 30 wt% Ga2O3, which corresponds to a theoretical monolayer coverage. Gallium oxide highly dispersed on Al2O3 is considered to be responsible for the high activity and selectivity. The reaction characteristics of Ga2O3/Al2O3 were studied and compared with Ga-ZSM-5 and Co-ZSM-5. Ga2O3/Al2O3 exhibited the highest activity and selectivity at high temperature. In addition, Ga2O3/Al2O3 showed higher tolerance against water than Ga-ZSM-5. C3H8 and C3H6 were also evaluated as reducing agents, and Ga2O3/Al2O3 showed higher activity than Ga-ZSM-5 above 723 K achieving almost complete reduction of NO to N-2. (C) 1998 Elsevier Science B.V.