Raskar, R.Y. and Kale, K.B. and Gaikwad, A.G. (2012) De-oxygenation of CO2 by using Hydrogen, Carbon and Methane over Alumina-Supported Catalysts. Bulletin of Chemical Reaction Engineering and Catalysis, 7 (1). pp. 59-60. ISSN 1978-2993
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Abstract
The de-oxygenation of CO2 was explored by using hydrogen, methane, carbon etc., over alumina supported catalysts. The alumina-supported ruthenium, rhodium, platinum, molybdenum, vanadium and magnesium catalysts were first reduced in hydrogen atmosphere and then used for the de-oxygenation of CO2. Furthermore, experimental variables for the de-oxygenation of CO2 were temperature (range 50 to 650 oC), H2/CO2 mole ratios (1.0 to 5), and catalyst loading (0.5 to 10 wt %). During the de-oxygenation of CO2 with H2 or CH4 or carbon, conversion of CO2, selectivity to CO and CH4 were estimated. Moreover, 25.4 % conversion of CO2 by hydrogen was observed over 1 wt% Pt/Al2O3 catalyst at 650 oC with 33.8 % selectivity to CH4. However, 8.1 to 13.9 % conversion of CO2 was observed over 1 wt% Pt/Al2O3 catalyst at 550 oC in the presence of both H2 and CH4. Moreover, 42.8 to 79.4 % CH4 was converted with 9 to 23.1 % selectivity to CO. It was observed that the de-oxygenation of CO2 by hydrogen, carbon and methane produced carbon, CO and CH4. © 2012 BCREC UNDIP. All rights reserved
Item Type: | Article |
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Uncontrolled Keywords: | De-oxygenation of carbon dioxide, hydrogen and methane; ruthenium, rhodium, platinum molybdenum, vanadium, magnesium, and alumina — supported catalysts |
Subjects: | T Technology > TP Chemical technology Q Science > QD Chemistry |
Divisions: | UNDIP Journal > Bulletin of Chemical Reaction Engineering and Catalysis Faculty of Engineering > Department of Chemical Engineering Faculty of Engineering > Department of Chemical Engineering |
ID Code: | 35720 |
Deposited By: | Dr. Istadi Istadi |
Deposited On: | 11 Jul 2012 14:59 |
Last Modified: | 16 Mar 2016 11:09 |
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