dc.contributorUniversidade Federal de Lavras (UFLA)
dc.contributorUniversidade Estadual de Campinas (UNICAMP)
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.contributorNatl Univ La Plata
dc.date.accessioned2014-05-20T14:18:28Z
dc.date.available2014-05-20T14:18:28Z
dc.date.created2014-05-20T14:18:28Z
dc.date.issued2009-03-31
dc.identifierApplied Catalysis A-general. Amsterdam: Elsevier B.V., v. 357, n. 1, p. 79-84, 2009.
dc.identifier0926-860X
dc.identifierhttp://hdl.handle.net/11449/25562
dc.identifier10.1016/j.apcata.2009.01.014
dc.identifierWOS:000264558200011
dc.description.abstractA series of Nb-containing hematites, Fe-2-xNbxO3 (%Nb = 0.00, 1.49, 5.00 and 9.24) was prepared using the conventional co-precipitation method. Mossbauer and temperature-programmed reduction (TPR) measurements suggested the formation of the crystalline phase with partial substitution of Fe3+ by Nb5+ in the structure. N-2 adsorption/desorption revealed that the presence of Nb has a remarkable effect on the textural properties of the material with an increase in the BET surface area. The reactivity of Fe2-xNbxO3 was investigated using the oxidation of the methylene blue dye used as a model pollutant. The obtained results showed that the presence of Nb seems not to act directly promoting the H2O2 decomposition, but improving the dye oxidation. The analysis using the ESI-MS technique showed partial oxidation observed through different intermediates before the mineralization. This suggests the use of Nb-doped hematite as an efficient catalyst in degradation reactions in the presence of H2O2 or ultraviolet light. (C) 2009 Elsevier B.V. All rights reserved.
dc.languageeng
dc.publisherElsevier B.V.
dc.relationApplied Catalysis A: General
dc.relation4.521
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.subjectHematite
dc.subjectNiobium
dc.subjectOrganic oxidation
dc.subjectESI-MS
dc.titleNb-containing hematites Fe2-xNbxO3: The role of Nb5+ on the reactivity in presence of the H2O2 or ultraviolet light
dc.typeArtículos de revistas


Este ítem pertenece a la siguiente institución