A study of the nature of the oxidant in V2O5-MoO3/Al2O3 catalyst
The nature of the oxidising species in/on a V2O5-MoO3/ Al2O3 catalyst has been studied by using the combination of transient kinetic techniques (i) oxygen temperature programmed desorption (TPD), (ii) temperature programmed reduction (TPR) and (iii) temperature programmed oxidation (TPO). The oxygen...
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
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Elsevier BV
2001
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| Online Access: | http://psasir.upm.edu.my/id/eprint/115198/ http://psasir.upm.edu.my/id/eprint/115198/1/115198.pdf |
| _version_ | 1848866712548540416 |
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| author | Taufiq-Yap, Y.H. Waugh, K.C. |
| author_facet | Taufiq-Yap, Y.H. Waugh, K.C. |
| author_sort | Taufiq-Yap, Y.H. |
| building | UPM Institutional Repository |
| collection | Online Access |
| description | The nature of the oxidising species in/on a V2O5-MoO3/ Al2O3 catalyst has been studied by using the combination of transient kinetic techniques (i) oxygen temperature programmed desorption (TPD), (ii) temperature programmed reduction (TPR) and (iii) temperature programmed oxidation (TPO). The oxygen TPD spectrum observed two molecular oxygen species having desorption peak maxima of 774 and 825 K. Three peak maxima (705, 915 and 1120 K) were observed in the rate of anaerobic oxidation of CO indicating that three types of kinetically different oxygen states exist in the catalyst. Re-oxidation of CO reduced the material by N2O and resulted in the replacement of the lattice oxygen by N2O, the re-oxidation occurring at 683; 798 and 918 K, but does not reproduce the original morphology of the catalyst. |
| first_indexed | 2025-11-15T14:24:57Z |
| format | Article |
| id | upm-115198 |
| institution | Universiti Putra Malaysia |
| institution_category | Local University |
| language | English |
| last_indexed | 2025-11-15T14:24:57Z |
| publishDate | 2001 |
| publisher | Elsevier BV |
| recordtype | eprints |
| repository_type | Digital Repository |
| spelling | upm-1151982025-02-26T03:05:20Z http://psasir.upm.edu.my/id/eprint/115198/ A study of the nature of the oxidant in V2O5-MoO3/Al2O3 catalyst Taufiq-Yap, Y.H. Waugh, K.C. The nature of the oxidising species in/on a V2O5-MoO3/ Al2O3 catalyst has been studied by using the combination of transient kinetic techniques (i) oxygen temperature programmed desorption (TPD), (ii) temperature programmed reduction (TPR) and (iii) temperature programmed oxidation (TPO). The oxygen TPD spectrum observed two molecular oxygen species having desorption peak maxima of 774 and 825 K. Three peak maxima (705, 915 and 1120 K) were observed in the rate of anaerobic oxidation of CO indicating that three types of kinetically different oxygen states exist in the catalyst. Re-oxidation of CO reduced the material by N2O and resulted in the replacement of the lattice oxygen by N2O, the re-oxidation occurring at 683; 798 and 918 K, but does not reproduce the original morphology of the catalyst. Elsevier BV 2001 Article PeerReviewed text en http://psasir.upm.edu.my/id/eprint/115198/1/115198.pdf Taufiq-Yap, Y.H. and Waugh, K.C. (2001) A study of the nature of the oxidant in V2O5-MoO3/Al2O3 catalyst. Chemical Engineering Science, 56 (20). pp. 5787-5792. ISSN 0009-2509 https://linkinghub.elsevier.com/retrieve/pii/S0009250901002627 10.1016/S0009-2509(01)00262-7 |
| spellingShingle | Taufiq-Yap, Y.H. Waugh, K.C. A study of the nature of the oxidant in V2O5-MoO3/Al2O3 catalyst |
| title | A study of the nature of the oxidant in V2O5-MoO3/Al2O3 catalyst |
| title_full | A study of the nature of the oxidant in V2O5-MoO3/Al2O3 catalyst |
| title_fullStr | A study of the nature of the oxidant in V2O5-MoO3/Al2O3 catalyst |
| title_full_unstemmed | A study of the nature of the oxidant in V2O5-MoO3/Al2O3 catalyst |
| title_short | A study of the nature of the oxidant in V2O5-MoO3/Al2O3 catalyst |
| title_sort | study of the nature of the oxidant in v2o5-moo3/al2o3 catalyst |
| url | http://psasir.upm.edu.my/id/eprint/115198/ http://psasir.upm.edu.my/id/eprint/115198/ http://psasir.upm.edu.my/id/eprint/115198/ http://psasir.upm.edu.my/id/eprint/115198/1/115198.pdf |