Abstract
A novel precipitation/digestion route has been developed to synthesize crystalline cerium hydroxy carbonate (CHC: Ce(OH)CO3) by using an equimolar quantity of cerium nitrate (Ce(NO3)3·6H2O) and mixed precipitants (KOH + K2CO3) at room temperature. Nano-sized CeO2 supports could be prepared by the pre-calcination of CHC at 400 °C for 4 h. A highly active water gas shift (WGS) catalyst, 1 wt.% Pt/CeO2 catalyst showed almost equilibrium CO conversion with 100% CO2 selectivity at 320 °C even at the gas hourly space velocity (GHSV) of 45,625 h−1.
Graphical Abstract
A novel precipitation/digestion route has been developed to synthesize crystalline cerium hydroxy carbonate (CHC: Ce(OH)CO3) by using an equimolar quantity of cerium nitrate (Ce(NO3)3·6H2O) and mixed precipitants (KOH + K2CO3) at room temperature. Nano-sized CeO2 supports could be prepared by the pre-calcination of CHC at 400 °C for 4 h. A highly active water gas shift (WGS) catalyst, 1 wt.% Pt/CeO2 catalyst showed almost equilibrium CO conversion with 100% CO2 selectivity at 320 °C even at the gas hourly space velocity (GHSV) of 45,625 h−1.
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Acknowledgments
This work is financially supported by Korea Ministry of Environment (MOE) as “Human Resource Development Project for Energy from Waste & Recycling”. This research was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science and Technology (2010-0002521). This work was supported by The Korean Federation of Science and Technology Societies Grant funded by Korea Government (MEST, Basic Research Promotion Fund).
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Potdar, H.S., Jeong, DW., Kim, KS. et al. Synthesis of Highly Active Nano-Sized Pt/CeO2 Catalyst via a Cerium Hydroxy Carbonate Precursor for Water Gas Shift Reaction. Catal Lett 141, 1268–1274 (2011). https://doi.org/10.1007/s10562-011-0656-5
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DOI: https://doi.org/10.1007/s10562-011-0656-5