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dc.contributor.authorGonzález García, Belén-
dc.contributor.authorGrasa Adiego, Gemma-
dc.contributor.authorAlonso Carreño, Mónica-
dc.contributor.authorAbanades García, Juan Carlos-
dc.date.accessioned2009-02-27T16:08:51Z-
dc.date.available2009-02-27T16:08:51Z-
dc.date.issued2008-11-03-
dc.identifier.citationIndustrial and Engineering Chemistry Research 47(23): 9256-9262 (2008)en_US
dc.identifier.issn0888-5885-
dc.identifier.urihttp://hdl.handle.net/10261/11106-
dc.description7 pages, 8 figures.-- Printed version published Dec 3, 2008.en_US
dc.description.abstractCalcium oxide is being proposed as a regenerable sorbent for CO2 at high temperatures via a carbonation/calcination loop. It is well-known that natural sorbents lose their capacity to capture CO2 as the number of the carbonation/calcination cycles increases. The equations proposed in the literature to describe this decay are limited to moderate calcination temperatures (typically well below 950°C). This work studies the effect of the calcination temperature and calcination time when the temperatures exceed 950°C. Such high regeneration temperatures are necessary in some of the most efficient processes proposed, and they are shown to strongly affect sorbent performance. We propose a model to describe maximum sorbent conversion as a function of the number of cycles, the calcination temperature, and the calcination time. This model combines existing knowledge about the decay of sorbent activity under moderate calcination temperatures with the effect of sintering in each cycle.en_US
dc.description.sponsorshipThis work is partially funded by the European Commision (C3-Capture). B.G. acknowledges a predoctoral research grant from FICYT.en_US
dc.format.extent918459 bytes-
dc.format.mimetypeapplication/pdf-
dc.language.isoengen_US
dc.publisherAmerican Chemical Societyen_US
dc.rightsclosedAccessen_US
dc.titleModeling of the Deactivation of CaO in a Carbonate Loop at High Temperatures of Calcinationen_US
dc.typeartículoen_US
dc.identifier.doi10.1021/ie8009318-
dc.description.peerreviewedPeer revieweden_US
dc.relation.publisherversionhttp://dx.doi.org/10.1021/ie8009318en_US
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