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Calorimetry, activity, and micro-FTIR analysis of CO chemisorption, titration, and oxidation on supported PtThe value of in situ analysis on CO chemisorption, titration and oxidation over supported Pt catalysts using calorimetry, catalytic and micro-FTIR methods is illustrated using silica- and titania-supported samples. Isothermal CO-O and O2-CO titrations have not been widely used on metal surfaces and may be complicated if some oxide supports are reduced by CO titrant. However, they can illuminate the kinetics of CO oxidation on metal/oxide catalysts since during such titrations all O and CO coverages are scanned as a function of time. There are clear advantages in following the rates of the catalyzed CO oxidation via calorimetry and gc-ms simultaneously. At lower temperatures the evidence they provide is complementary. CO oxidation and its catalysis of CO oxidation have been extensively studied with hysteresis and oscillations apparent, and the present results suggest the benefits of a combined approach. Silica support porosity may be important in defining activity-temperature hysteresis. FTIR microspectroscopy reveals the chemical heterogeneity of the catalytic surfaces used; it is interesting that the evidence with regard to the dominant CO surface species and their reactivities with regard to surface oxygen for present oxide-supported Pt are different from those seen on graphite-supported Pt.
Document ID
19900015290
Acquisition Source
Legacy CDMS
Document Type
Conference Paper
Authors
Sermon, Paul A.
(Brunel Univ. Uxbridge, United Kingdom)
Self, Valerie A.
(Brunel Univ. Uxbridge, United Kingdom)
Vong, Mariana S. W.
(Brunel Univ. Uxbridge, United Kingdom)
Wurie, Alpha T.
(Brunel Univ. Uxbridge, United Kingdom)
Date Acquired
September 6, 2013
Publication Date
June 1, 1990
Publication Information
Publication: NASA, Langley Research Center, Low-Temperature CO-Oxidation Catalysts for Long-Life CO2 Lasers
Subject Category
Inorganic And Physical Chemistry
Accession Number
90N24606
Distribution Limits
Public
Copyright
Work of the US Gov. Public Use Permitted.
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