Role of phosphorus in carbon matrix in desulfurization of diesel fuel using adsorption process

Adsorptive removal of dibenzothiophene (DBT) and 4,6-dimethyldibenzothiophene (DMDBT) from model diesel fuel with 20 ppmw total concentration of sulfur was investigated on polymer-derived carbons with incorporated heteroatoms of oxygen, sulfur and phosphorus. The materials before and after exposure...

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Detalles Bibliográficos
Autores: Seredych, Mykola, Wu, Zoe, Brender, Patrice, Ovín Ania, María Concepción, Vix-Guterl, Cathie, Bandosz, Teresa J.
Tipo de recurso: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:2012
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/99404
Acceso en línea:http://hdl.handle.net/10261/99404
Access Level:acceso abierto
Palabra clave:Dibenzothiophenes
Model diesel fuel
Activated carbon
P-functionalities
Reactive adsorption
Descripción
Sumario:Adsorptive removal of dibenzothiophene (DBT) and 4,6-dimethyldibenzothiophene (DMDBT) from model diesel fuel with 20 ppmw total concentration of sulfur was investigated on polymer-derived carbons with incorporated heteroatoms of oxygen, sulfur and phosphorus. The materials before and after exposure to model diesel fuel were characterized using adsorption of nitrogen, thermal analysis, potentiometric titration, XPS and elemental analysis. The selectivities for DBT and DMDBT adsorption were calculated with reference to naphthalene. The results indicated that the presence of phosphorus, especially in the form of pyrophosphates and P2O5, increases the capacity and selectivity for removal of dibenzothiophenes. It also affects the adsorption mechanism. Phosphorus suppresses oxidation reactions of DBT and DMDBT. Owing to a possible location of bulky phosphorus groups in pore with sizes between 1 and 3 nm thiophenic molecules are strongly adsorbed there via dispersive forces. Acidic environment also enhances adsorption via acid–base interactions. Physical adsorption mechanism and stability of surface make these carbons attractive candidates for thermal regeneration.