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The co-electrolysis of CO2–H2O to methane via a novel micro-tubular electrochemical reactor.
- Source :
- Journal of Materials Chemistry A; 2/14/2017, Vol. 5 Issue 6, p2904-2910, 7p
- Publication Year :
- 2017
-
Abstract
- Efficient and direct conversion of CO<subscript>2</subscript> to hydrocarbons through electrolysis is a promising approach for energy storage and CO<subscript>2</subscript> utilization. In this study, high temperature co-electrolysis of H<subscript>2</subscript>O–CO<subscript>2</subscript> and low temperature methanation processes are synergistically integrated in a micro-tubular reactor. The temperature gradient along the micro-tubular reactor provides favorable conditions for both the electrolysis and methanation reactions. Moreover, the micro-tubular reactor can provide high volumetric factor for both the electrolysis and methanation processes. When the cathode of the micro-tubular reactor is fed with a stream of 10.7% CO<subscript>2</subscript>, 69.3% H<subscript>2</subscript> and 20.0% H<subscript>2</subscript>O, an electrolysis current of −0.32 A improves CH<subscript>4</subscript> yield from 12.3% to 21.1% and CO<subscript>2</subscript> conversion rate from 64.9% to 87.7%, compared with the operation at open circuit voltage. Furthermore, the effects of the inlet gas composition in the cathode on the CO<subscript>2</subscript> conversion rate and the CH<subscript>4</subscript> yield are systematically investigated. Higher ratio of H : C in the inlet results in higher CO<subscript>2</subscript> conversion rate. Among all the cases studied, the highest CH<subscript>4</subscript> yield of 23.1% has been achieved when the inlet gas in the cathode is consisted of 21.3% CO<subscript>2</subscript>, 58.7% H<subscript>2</subscript> and 20.0% H<subscript>2</subscript>O with an electrolysis current of −0.32 A. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 20507488
- Volume :
- 5
- Issue :
- 6
- Database :
- Complementary Index
- Journal :
- Journal of Materials Chemistry A
- Publication Type :
- Academic Journal
- Accession number :
- 121194606
- Full Text :
- https://doi.org/10.1039/c6ta10252b