A catalytic membrane reactor for water-gas shift reaction

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We conducted the WGS reaction on a catalytic membrane reactor consisting of a WGS catalyst bed, Pt/CeO(2) and thin, defect-free, Pd-Cu alloy membranes. The presence of CO and other gases with H(2) reduced the H(2) permeation through the membrane by more than 50% and the effect of the other gases on the permeation reduction decreased in the following order: CO > CO(2)> N(2). In a catalytic membrane reactor with helium sweep gas, the CO conversion was improved by about 65% compared with the catalyst without any membrane, and the CH(4) formed from an undesirable side reaction was significantly reduced. Although the H(2) permeation was severely reduced by surface phenomena such as blocking of available H(2) dissociation sites by CO, CO(2) and steam, the CO conversion was notably improved by the membrane presence. Moreover, the CO conversion was maintained at 98% even after 60 h of reaction and our Pd-Cu-Ni alloy membrane withstood the exposure of CO and the other gases. However, for separation of pure H(2), a newly designed, catalyst-membrane system is required with better sealing and the ability to withstand the high operating pressure that drives the H(2) permeation.
Publisher
Springer
Issue Date
2010-05
Language
English
Article Type
Article
Keywords

POROUS NICKEL SUPPORT; TERNARY ALLOY MEMBRANE; HYDROGEN PERMEATION; PRECIOUS METALS; MASS-TRANSFER; THIN PD/AG; CU-REFLOW; TEMPERATURE; SEPARATION; STEAM

Citation

KOREAN JOURNAL OF CHEMICAL ENGINEERING, v.27, no.3, pp.816 - 821

ISSN
0256-1115
DOI
10.1007/s11814-010-0133-7
URI
http://hdl.handle.net/10203/24164
Appears in Collection
CBE-Journal Papers(저널논문)
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