The co-electrolysis of CO2-H2O to methane via a novel micro-tubular electrochemical reactor
Efficient and direct conversion of CO 2 to hydrocarbons through electrolysis is a promising approach for energy storage and CO 2 utilization. In this study, high temperature co-electrolysis of H 2 O-CO 2 and low temperature methanation processes are synergistically integrated in a micro-tubular reac...
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Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2017, Vol.5 (6), p.294-291 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Efficient and direct conversion of CO
2
to hydrocarbons through electrolysis is a promising approach for energy storage and CO
2
utilization. In this study, high temperature co-electrolysis of H
2
O-CO
2
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
2
, 69.3% H
2
and 20.0% H
2
O, an electrolysis current of −0.32 A improves CH
4
yield from 12.3% to 21.1% and CO
2
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
2
conversion rate and the CH
4
yield are systematically investigated. Higher ratio of H : C in the inlet results in higher CO
2
conversion rate. Among all the cases studied, the highest CH
4
yield of 23.1% has been achieved when the inlet gas in the cathode is consisted of 21.3% CO
2
, 58.7% H
2
and 20.0% H
2
O with an electrolysis current of −0.32 A.
Efficient and direct conversion of CO
2
to hydrocarbons through electrolysis is a promising approach for energy storage and CO
2
utilization. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/c6ta10252b |