4.7 Article

Combined generation and separation of hydrogen in an electrochemical water gas shift reactor (EWGSR)

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 37, Issue 8, Pages 6635-6645

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2012.01.053

Keywords

Electrochemical water gas shift reactor; Hydrogen generation and separation; Electrochemical carbon monoxide oxidation; High temperature proton exchange membrane; Poly(2,5-benzimidazole); ABPBI; Platinum ruthenium catalyst

Funding

  1. Fraunhofer-Gesellschaft
  2. Max Planck Society in Germany

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Hydrogen rich gas, originating from fossil fuel reforming processes or biomass gasification, contains a significant amount of CO. Typically, the yield of H-2 is increased with subsequent water gas shift units, converting CO to CO2 and additional H-2. This study describes a new reactor concept enabling the water gas shift reaction and the separation of the generated hydrogen in one process step by using electrical energy. This electrochemical water gas shift reactor applies a H3PO4-doped Poly(2,5-benzimidazole) membrane as electrolyte and carbon supported Pt or PtRu as anode catalyst. The reactor operation was investigated at 130 degrees C and 150 degrees C with a H-2 free anode feed stream of humidified CO and N-2. The experimental results show the feasibility of the reactor concept, as H-2 was generated at the cathode according to Faradays Law. Anodic PtRu led to lower power demands than Pt. The operation at the two temperatures showed that 130 degrees C results in a lower electrical power demand while generating an equal amount of H-2. The feasibility of the reactor was assessed using exergy efficiency analysis. Copyright (C) 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

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