DSpace logo

Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/18822
Full metadata record
DC FieldValueLanguage
dc.contributor.authorKatayama, Akiko-
dc.contributor.authorKita, Hideaki-
dc.date.accessioned2025-04-29T06:29:05Z-
dc.date.available2025-04-29T06:29:05Z-
dc.date.issued1978-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/18822-
dc.description.abstractE.s.r. signals from a platinum–graphite catalyst (Pt–graphite) and pure graphite were observed as functions of hydrogen gas pressure, temperature and the amount of platinum. The signals were inferred to be due to conduction charge carriers. The e.s.r. signal of Pt–graphite exhibits behaviour similar to that of pure graphite with respect to the temperature variation of the g∥ value. The signal from pure graphite was not affected by the presence of hydrogen gas. However, the signal from Pt–graphite at g=ge(g value of a free electron) decreased with the amount of platinum and increased with the increment in hydrogen gas pressure, obeying the non-dissociative Langmuir isotherm. Detailed analysis indicated that the adsorption of hydrogen on Pt–graphite causes a change in the number of conduction electrons. Adsorbed hydrogen on Pt–graphite is concluded to be positively polarized in molecular form.en_US
dc.language.isoenen_US
dc.publisherJournal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1978, 74 (08)en_US
dc.subjectChemistryen_US
dc.subjectHydrogen adsorptionen_US
dc.subjectPlatinum–graphite catalysten_US
dc.subjectJournal of the Chemical Society : Faraday Transaction - Ien_US
dc.titleAdsorption of hydrogen on a platinum–graphite catalyst. Part 1.—Electron spin resonance measurement in the gas–solid systemen_US
dc.typeArticleen_US
Appears in Collections:Journal Articles (before-1995)

Files in This Item:
File Description SizeFormat 
1963-1972.pdf
  Restricted Access
620.79 kBAdobe PDFView/Open Request a copy


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.