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dc.contributor.authorRichardson, P. C.-
dc.contributor.authorRudham, R.-
dc.contributor.authorTullett, A. D.-
dc.date.accessioned2025-02-03T06:42:09Z-
dc.date.available2025-02-03T06:42:09Z-
dc.date.issued1972-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/17038-
dc.description.abstractThe reduction of rutile by vacuum outgassing between 450-825nC, or by hydrogen or carbon monoxide at 350 C, yields active catalysts for low temperature parahydrogen enrichment due to the presence of surface Ti3 b ions. Since the kinetics indicate saturation of these active sites, the absolute rate of enrichment at 77 K and 1.3 x 103 N m-2 can be taken as a direct measure of the extent of surface non-stoichiometry. Poisoning experiments with oxygen indicate Ti3+ ions are not limited to the surface layer alone, but arc distributed between surface and sub-surface layers, and are effectively mobile at temperatures considerably below the Tammann temperature. The activity for parahydrogen enrichment arising from oxygen molecules physically adsorbed on fully oxidised rutile has been used to derive an equation, which is used to estimate the concentration of Ti3+ ions in reduced surfaces. This did not exceed ~8.0 x 1016 ion m~2 for the most active surface studied.en_US
dc.language.isoenen_US
dc.publisherJournal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1972, 68 (12)en_US
dc.subjectChemistryen_US
dc.subjectParahydrogen Enrichmenten_US
dc.subjectNon Stoichiomctric Rutileen_US
dc.subjectJournal of the Chemical Society : Faraday Transaction - Ien_US
dc.titleLow Temperature Parahydrogen Enrichment on Non- stoichiomctric Rutileen_US
dc.typeArticleen_US
Appears in Collections:Journal Articles (before-1995)

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