Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/91712
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dc.titleSteady-state multiplicity in carbon monoxide oxidation over LaMnO3
dc.contributor.authorChuah, G.K.
dc.contributor.authorJaenicke, S.
dc.contributor.authorLee, J.Y.
dc.date.accessioned2014-10-09T08:21:19Z
dc.date.available2014-10-09T08:21:19Z
dc.date.issued1991-05-02
dc.identifier.citationChuah, G.K.,Jaenicke, S.,Lee, J.Y. (1991-05-02). Steady-state multiplicity in carbon monoxide oxidation over LaMnO3. Applied Catalysis 72 (1) : 51-61. ScholarBank@NUS Repository.
dc.identifier.issn01669834
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/91712
dc.description.abstractMultiple steady states have been observed during catalytic carbon monoxide oxidation over polycrystalline LaMnO3. The bistability was noted only at a carbon monoxide partial pressure Pco ≥ 46 kPa. The transition to the more reactive state sets in at 220°C. Upon cooling, the activity of the catalyst is sustained at a lower temperature than the ignition point. The width of the hysteresis loop increases with increasing carbon monoxide concentration. An oxidation/reduction mechanism is proposed whereby the high activity state is the surface-reduced form. The apparent activation energy is 16-19 kJ/mol for both steady states of the catalyst, indicating that a similar pathway for carbon monoxide oxidation is followed in the two states. © 1991.
dc.sourceScopus
dc.subjectcarbon monoxide oxidation
dc.subjectkinetics.
dc.subjectlanthanum manganese oxide
dc.subjectperovskites
dc.subjectsteady state (multiple)
dc.typeArticle
dc.contributor.departmentCHEMICAL ENGINEERING
dc.contributor.departmentCHEMISTRY
dc.description.sourcetitleApplied Catalysis
dc.description.volume72
dc.description.issue1
dc.description.page51-61
dc.identifier.isiutNOT_IN_WOS
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