Enhancing co-production of H2 and syngas via water splitting and POM on surface-modified oxygen permeable membranes

• Published in: AIChE journal Vol. 62; no. 12; pp. 4427 - 4435
• Main Authors: Wu, Xiao-Yu, Ghoniem, Ahmed F., Uddi, Mruthunjaya
• Format: Journal Article
• Language: English
• Published: New York Blackwell Publishing Ltd 01.12.2016; American Institute of Chemical Engineers
• Subjects: Acetal resins; Carbon dioxide; Carbon monoxide; catalyst; Catalysts; Decomposition; Fluctuations; Flux; Hydrogen; Hydrogen production; Low cycle fatigue; membrane reactor; Membranes; Methane; MIEC; Nickel; Oxidation; Oxygen; partial oxidation of methane; Penetration; Permeability; Splitting; Synthesis gas; Synthetic fuels; thermolysis; Water splitting
• ISSN: 0001-1541; 1547-5905
• DOI: 10.1002/aic.15518

In this article, we report a detailed study on co‐production of H2 and syngas on La0.9Ca0.1FeO3−δ (LCF‐91) membranes via water splitting and partial oxidation of methane, respectively. A permeation model shows that the surface reaction on the sweep side is the rate limiting step for this process on a 0.9 mm‐thick dense membrane at 990°C. Hence, sweep side surface modifications such as adding a porous layer and nickel catalysts were applied; the hydrogen production rate from water thermolysis is enhanced by two orders of magnitude to 0.37 μmol/cm2•s compared with the results on the unmodified membrane. At the sweep side exit, syngas (H2/CO = 2) is produced and negligible solid carbon is found. Yet near the membrane surface on the sweep side, methane can decompose into solid carbon and hydrogen at the surface, or it may be oxidized into CO and CO2, depending on the oxygen permeation flux. © 2016 American Institute of Chemical Engineers AIChE J, 62: 4427–4435, 2016