English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/87185
Share/Impact:
Statistics
logo share SHARE logo core CORE   Add this article to your Mendeley library MendeleyBASE

Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL
Exportar a otros formatos:
Title

Catalytic activity of ni-based oxygen-carriers for steam methane reforming in chemical-looping processes

AuthorsOrtiz Navarro, María; Diego Poza, Luis F. de ; Abad Secades, Alberto ; García Labiano, Francisco ; Gayán Sanz, Pilar ; Adánez Elorza, Juan
Issue Date2012
PublisherAmerican Chemical Society
CitationEnergy and Fuels 26(2) : 791- 800 (2012)
AbstractChemical-looping technology has been suggested as one of the most promising technologies for reducing the cost of CO 2 capture using fossil fuels. This technology involves the use of an oxygen-carrier, which transfers oxygen from air to the fuel avoiding the direct contact between them. Oxygen carriers based on nickel have been the most extensively analyzed in the literature because of their good performance working at high temperatures (900-1100 °C). It is well-known that Ni catalyzes steam methane reforming (SMR) and water-gas shift (WGS) reactions, which are produced both in chemical-looping combustion (CLC) and chemical-looping reforming (CLR) processes. In this work, the catalytic activity of two Ni-based oxygen-carriers prepared by impregnation, NiO18-αAl 2O 3 and NiO21-γAl 2O 3, with respect to SMR and WGS reactions, have been determined in a fixed-bed reactor at different operating conditions. The catalytic activity was similar for both oxygen-carriers but lower than that exhibited by conventional Ni catalysts. Nevertheless, the catalytic effect was of great relevance to achieve complete CH 4 conversion in CLC and CLR systems. In addition, it was found that the catalytic activity of the oxygen-carriers for the SMR depended on the oxidation degree of the oxygen-carrier. This fact must be considered when the SMR takes place simultaneously to the reduction of NiO. © 2011 American Chemical Society.
Description10 pages, 12 figures, 8 tables
URIhttp://hdl.handle.net/10261/87185
DOI10.1021/ef2013612
Identifiersdoi: 10.1021/ef2013612
issn: 0887-0624
Appears in Collections:(ICB) Artículos
Files in This Item:
File Description SizeFormat 
accesoRestringido.pdf15,38 kBAdobe PDFThumbnail
View/Open
Show full item record
Review this work
 

Related articles:


WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.