Please use this identifier to cite or link to this item: http://hdl.handle.net/1843/80372
Type: Artigo de Periódico
Title: Oxidative desulfurization of dibenzothiophene over highly dispersed Mo-doped graphitic carbon nitride
Authors: Diogo Augusto Fonseca Gonçalves
Mauricio Veloso Brant Pinheiro
Klaus Wilhelm Heinrich Krambrock
Rodrigo Ribeiro Resende
Breno Rodrigues Lamaghere Galvão
Eudes Lorençon
Abstract: Mo-doped graphitic carbon nitride (Mo/g-C3N4) was successfully prepared by thermal condensation of a Mo/melamine precursor in a semi-closed alumina crucible at 550 °C without atmosphere. Thermogravimetric analysis (TGA) was used to evaluate the polymerization route of the precursor, and theoretical and experimental investigations revealed that the Mo species were likely dispersed and anchored to the pyridinic groups of g-C3N4. As a result, the obtained Mo/g-C3N4 displayed exceptional catalytic activity in the oxidative desulfurization of dibenzothiophene (DBT) with H2O2. The effects of catalyst dosage, O/S ratio, and temperature on the catalytic properties of Mo/g-C3N4 were investigated. The kinetic studies revealed a pseudo-first-order kinetic process for DBT oxidation with an apparent activation energy of 43.6 kJ mol−1. Experimental and theoretical evaluation of the Mo/g-C3N4 stability suggests that catalytically active Mo species are progressively leached from the g-C3N4 structure. The decrease in the Mo–N bond order after forming reactive peroxo-Mo(VI) groups was associated with catalyst deactivation.
Subject: Nitreto de carbono
Dessulfuração
language: eng
metadata.dc.publisher.country: Brasil
Publisher: Universidade Federal de Minas Gerais
Publisher Initials: UFMG
metadata.dc.publisher.department: ICB - DEPARTAMENTO DE BIOQUÍMICA E IMUNOLOGIA
ICX - DEPARTAMENTO DE FÍSICA
Rights: Acesso Restrito
metadata.dc.identifier.doi: https://doi.org/10.1007/s11696-022-02113-3
URI: http://hdl.handle.net/1843/80372
Issue Date: 2022
metadata.dc.url.externa: https://link.springer.com/article/10.1007/s11696-022-02113-3
metadata.dc.relation.ispartof: Chemical Papers
Appears in Collections:Artigo de Periódico

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