INVESTIGADORES
SAMBETH Jorge Enrique
artículos
Título:
Catalytic oxidation of CH ,OH to HCOOCH 3 on V,O,: A
Autor/es:
SAMBETH, JORGE; JUAN, ALFREDO; GAMBARO, LUIS; THOMAS, HORACIO JORGE
Revista:
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
Editorial:
Elsevier
Referencias:
Lugar: Amsterdam; Año: 1995 vol. 118 p. 283 - 291
ISSN:
1381-1169
Resumen:
In a previous work, the CH,OH adsorption-oxidation process on V,O, was studied by mass spectrometry analysis of the interactaction atmosphere. The following partial oxidation products were reported: H&O, CO, CO,, (CH,O),CH, (methylal), CH,OCH,OH (hemimethylal) and HCOOCH,. The data so obtained allowed a reaction pathway to be proposed. In the present work, we used models of the plane (010) of V,O, and of CH,OH, to test whether the pathway proposed in this work as well as alternative ones presented by other authors were energetically favorable or not. With this purpose, the variation of the total system energy was computed in each step by extended Hickel-type calculations (ASED, atom superposition and electron delocalization). The results showed, on the one hand, that the pathway proposed in this work is better than alternatives pathways, and on the other hand, the possible existence of other equally-favorable adsorption sites in which bridge oxygen may take part. interactaction atmosphere. The following partial oxidation products were reported: H&O, CO, CO,, (CH,O),CH, (methylal), CH,OCH,OH (hemimethylal) and HCOOCH,. The data so obtained allowed a reaction pathway to be proposed. In the present work, we used models of the plane (010) of V,O, and of CH,OH, to test whether the pathway proposed in this work as well as alternative ones presented by other authors were energetically favorable or not. With this purpose, the variation of the total system energy was computed in each step by extended Hickel-type calculations (ASED, atom superposition and electron delocalization). The results showed, on the one hand, that the pathway proposed in this work is better than alternatives pathways, and on the other hand, the possible existence of other equally-favorable adsorption sites in which bridge oxygen may take part.