نتایج جستجو برای: co preferential oxidation
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Catalytic, low temperature preferential oxidation (PROX) of carbon monoxide by aqueous [5,10,15,20-tetrakis(4-sulfonatophenyl)-2,3,7,8,12,13,17,18-octafluoroporphyrinato]rhodium(III) tetrasodium salt, (1[Rh(III)]) and [5,10,15,20-tetrakis(3-sulfonato-2,6-difluorophenyl)-2,3,7,8,12,13,17,18-octafluoroporphyrinato]rhodium(III) tetrasodium salt, (2[Rh(III)]) is reported. The PROX reaction occurs a...
Preferential oxidation of CO in the presence of excess hydrogen was studied on Pt/CeO2 with 5% metal loading. Catalytic data were similar to those observed on 1% Pt/CeO2 earlier [Wootsch et al. J. Catal. 225 (2004) 259]. The optimum temperature region is T≤373 K; conversion and selectivity of CO oxidation strongly decreased at higher temperatures. High-pressure XPS indicated CO adsorbed on plat...
Active Pt-based catalysts at low temperature towards the preferential oxidation of carbon monoxide in hydrogen-rich stream reaction (CO-PROX) are great importance for H2-fueled fuel cells, but still remain a challenge. Herein, we propose simple approach to synthesize highly active Pt20Fe/CeO2 catalyst employing borohydride reduction process. Transmission electronic microscopy revealed monodispe...
Industrial hydrogen production through methane steam reforming exceeds 50 million tons annually and accounts for 2-5% of global energy consumption. The hydrogen product, even after processing by the water-gas shift, still typically contains ∼1% CO, which must be removed for many applications. Methanation (CO + 3H2 → CH4 + H2O) is an effective solution to this problem, but consumes 5-15% of the ...
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