Use este identificador para citar ou linkar para este item: http://www.repositorio.ufop.br/jspui/handle/123456789/5119
Título: Cobalt-catalyzed oxidation of terpenes : Co-MCM-41 as an efficient shape-selective heterogeneous catalyst for aerobic oxidation of isolongifolene under solvent-free conditions.
Autor(es): Robles Azocar, Patrícia Alejandra
Rocha, Kelly Alessandra da Silva
Sousa, Edésia Martins Barros de
Gusevskaya, Elena Vitalievna
Palavras-chave: Isolongifolene
Autoxidation
Cobalt catalysts
Data do documento: 2009
Referência: ROBLES AZOCAR, P. A. et al. Cobalt-catalyzed oxidation of terpenes: Co-MCM-41 as an efficient shape-selective heterogeneous catalyst for aerobic oxidation of isolongifolene under solvent-free conditions. Journal of Catalysis, v. 265, p. 72-79, 2009. Disponível em: <http://www.sciencedirect.com/science/article/pii/S0021951709001249>. Acesso em: 02 fev. 2015.
Resumo: Cobalt-containing MCM-41 was used as a heterogeneous catalyst for the liquid-phase aerobic oxidation of isolongifolene, one of the most available sesquiterpenes. The material was prepared by direct incorporation of cobalt into the framework through the hydrothermal method, and was characterized by ICPAES, N2 adsorption–desorption, TEM, XRD, SAXS, XPS, and H2-TPR techniques. Characterizations suggest that cobalt introduced into MCM-41 exists mainly in a single-site Co2+ state, whereas the amounts of the extraframework Co3O4 are relatively low. The oxidation of isolongifolene under mild solvent-free conditions results mainly (90% selectivity) in isolongifolen-9-one, a compound which occupies a vintage place in modern perfume industry. The total concentration of oxygenated products in the final mixtures reaches 90 wt%. The catalyst undergoes no metal leaching, and can be easily recovered and re-used. A silica- included cobalt catalyst prepared through a conventional sol–gel method shows a catalytic activity comparable with that of Co-MCM-41; however, selectivity is much lower.
URI: http://www.repositorio.ufop.br/handle/123456789/5119
DOI: https://doi.org/10.1016/j.jcat.2009.04.012
ISSN: 0021-9517
Licença: O periódico Journal of Catalysis concede permissão para depósito deste artigo no Repositório Institucional da UFOP. Número da licença: 3581990164752.
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