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dc.contributor.authorK. Punyawudhoen_US
dc.contributor.authorJ. R. Monnieren_US
dc.contributor.authorJ. W.Van Zeeen_US
dc.date.accessioned2018-09-04T04:18:57Z-
dc.date.available2018-09-04T04:18:57Z-
dc.date.issued2011-03-15en_US
dc.identifier.issn15205827en_US
dc.identifier.issn07437463en_US
dc.identifier.other2-s2.0-79952583345en_US
dc.identifier.other10.1021/la104637wen_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79952583345&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/49841-
dc.description.abstractAdsorption of SO2on a Pt/C catalyst typically used in proton exchange- membrane fuel cells (PEMFCs) has been investigated by temperature programmed desorption (TPD). SO2concentrations in N2were varied from 5 ppm to 1% (vol) and adsorption isotherms were determined at 25, 50, and 80 °C. Oxygen assisted (O-assisted) desorption experiments (i.e., successive TPD experiments following exposure to room temperature O2after the first TPD event) produced an additional SO2peak at a temperature higher than the initial SO2peak. These two types of SO2adsorption were identified as weakly adsorbed SO2species desorbed between 140 and 200 °C, depending on concentration, and a strongly adsorbed, dissociated species. For the strongly adsorbed, dissociative species,18O2isotope introduction during O-assisted desorption yielded ratios of 50%, 36%, and 14% for SO2masses of 64, 66, and 68, respectively. The activation energy and kinetic constant of desorption are reported for weakly adsorbed SO2at 1% and 20 ppm SO2using the Polanyi-Wigner equation. © 2011 American Chemical Society.en_US
dc.subjectChemistryen_US
dc.subjectMaterials Scienceen_US
dc.subjectPhysics and Astronomyen_US
dc.titleSO<inf>2</inf>adsorption on carbon-supported Pt electrocatalystsen_US
dc.typeJournalen_US
article.title.sourcetitleLangmuiren_US
article.volume27en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsUniversity of South Carolinaen_US
Appears in Collections:CMUL: Journal Articles

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