CuO/cryptomelane catalyst for preferential oxidation of CO in the presence of H2: deactivation and regeneration

Empreu sempre aquest identificador per citar o enllaçar aquest ítem
Información del item - Informació de l'item - Item information
Títol: CuO/cryptomelane catalyst for preferential oxidation of CO in the presence of H2: deactivation and regeneration
Autors: Davó-Quiñonero, Arantxa | Navlani García, Miriam | Lozano Castelló, Dolores | Bueno López, Agustín
Grups d'investigació o GITE: Materiales Carbonosos y Medio Ambiente
Centre, Departament o Servei: Universidad de Alicante. Departamento de Química Inorgánica | Universidad de Alicante. Instituto Universitario de Materiales
Paraules clau: CuO/cryptomelane catalysts | Preferential oxidation | CO | H2
Àrees de coneixement: Química Inorgánica
Data de publicació: 11-d’abril-2016
Editor: Royal Society of Chemistry
Citació bibliogràfica: Catalysis Science & Technology. 2016, 6: 5684-5692. doi:10.1039/C6CY00329J
Resum: Cryptomelane and CuO/cryptomelane catalysts have been tested in the preferential oxidation of CO in the presence of H2 (CO-PROX reaction), paying special attention to deactivation and regeneration issues. Cryptomelane was stable during the CO-PROX reactions in ramp experiments until 200 °C and in a long-term isothermal experiment (10 h). Changes neither in the H2 reducibility and porosity nor in the crystalline phases detected by XRD were observed. On the contrary, CuO/cryptomelane was partially deactivated during the consecutive CO-PROX reaction cycles performed until 200 °C, and the catalytic activity was partially restored by reoxidising the catalyst at 200 °C or 400 °C, the latter temperature being more effective. In spite of the CuO/cryptomelane partial deactivation, the CO-PROX activity of this catalyst was higher than that of cryptomelane once a stable behaviour was achieved. The partial deactivation of CuO/cryptomelane was attributed to the segregation of crystalline phases (hausmannite (Mn3O4) and/or hopcalite (CuMn2O4)), with the segregation of potassium to the surface and decrease in the copper cations' reducibility. The potential contribution to deactivation of the changes in the porous texture of CuO/cryptomelane was ruled out.
Patrocinadors: The authors are thankful for the financial support from Generalitat Valenciana (Project PROMETEOII/2014/010), the Spanish Ministry of Economy and Competitiveness (Project MAT2014-61992-EXP and CTQ2015-67597-C2-2-R), the Spanish Ministry of Education, Culture and Sports (grant FPU14/01178), the Spanish Catalysis Society (SECAT TFM 2015), and the UE (FEDER funding).
ISSN: 2044-4753 (Print) | 2044-4761 (Online)
DOI: 10.1039/C6CY00329J
Idioma: eng
Tipus: info:eu-repo/semantics/article
Drets: This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence.
Revisió científica: si
Versió de l'editor:
Apareix a la col·lecció: INV - MCMA - Artículos de Revistas

Arxius per aquest ítem:
Arxius per aquest ítem:
Arxiu Descripció Tamany Format  
Thumbnail2016_Davo_etal_CatalSciTechnol.pdf1,72 MBAdobe PDFObrir Vista prèvia

Tots els documents dipositats a RUA estan protegits per drets d'autors. Alguns drets reservats.