Model for self-reactivation of highly sintered CaO particles during CO2 capture looping cycles

[EN] Calcium looping is an emerging high-temperature, energy-efficient, CO2 capture technology using CaO as a regenerable sorbent of CO2 through the reversible carbonation/calcination reaction. The stability of the sorbent plays a key role in the design of these systems. This paper revisits the self-reactivation phenomenon that has been reported for some highly deactivated CaO materials when submitted to repeated carbonation/calcination cycles under certain conditions. Self-reactivation is modelled in this paper as the result of a dynamic balance between the loss of activity in one cycle and the accumulated gain of activity by extended carbonation times, due to a product layer of CaCO3 that keeps building up on all surfaces, controlled by the slow diffusion of CO2. The model describes reasonably well the trends observed for some limestones and conditions. For other limestones and conditions, the carbonation mechanism is more complex and the model does not fit the evolution of the maximum Ca conversion with the number of cycles as well, although the general patterns of selfreactivation are still well reproduced.

Saved in:
Bibliographic Details
Main Authors: Arias Rozada, Borja, Abanades García, Juan Carlos, Anthony, Edward J.
Format: artículo biblioteca
Language:English
Published: American Chemical Society 2011-03-10
Subjects:CO2 capture, Ca-looping, Self-reactivation,
Online Access:http://hdl.handle.net/10261/40626
Tags: Add Tag
No Tags, Be the first to tag this record!
id dig-incar-es-10261-40626
record_format koha
spelling dig-incar-es-10261-406262018-11-15T07:44:14Z Model for self-reactivation of highly sintered CaO particles during CO2 capture looping cycles Arias Rozada, Borja Abanades García, Juan Carlos Anthony, Edward J. CO2 capture Ca-looping Self-reactivation [EN] Calcium looping is an emerging high-temperature, energy-efficient, CO2 capture technology using CaO as a regenerable sorbent of CO2 through the reversible carbonation/calcination reaction. The stability of the sorbent plays a key role in the design of these systems. This paper revisits the self-reactivation phenomenon that has been reported for some highly deactivated CaO materials when submitted to repeated carbonation/calcination cycles under certain conditions. Self-reactivation is modelled in this paper as the result of a dynamic balance between the loss of activity in one cycle and the accumulated gain of activity by extended carbonation times, due to a product layer of CaCO3 that keeps building up on all surfaces, controlled by the slow diffusion of CO2. The model describes reasonably well the trends observed for some limestones and conditions. For other limestones and conditions, the carbonation mechanism is more complex and the model does not fit the evolution of the maximum Ca conversion with the number of cycles as well, although the general patterns of selfreactivation are still well reproduced. This work is partially supported by the European Commission under the 7th Framework Programme (CaOling project). Peer reviewed 2011-10-05T10:58:56Z 2011-10-05T10:58:56Z 2011-03-10 artículo http://purl.org/coar/resource_type/c_6501 Energy and Fuels 25(4) : 1926-1930(2011) 0887-0624 http://hdl.handle.net/10261/40626 en #PLACEHOLDER_PARENT_METADATA_VALUE# info:eu-repo/grantAgreement/EC/FP7/241302 http://pubs.acs.org/doi/abs/10.1021/ef200015a open American Chemical Society
institution INCAR ES
collection DSpace
country España
countrycode ES
component Bibliográfico
access En linea
databasecode dig-incar-es
tag biblioteca
region Europa del Sur
libraryname Biblioteca del INCAR España
language English
topic CO2 capture
Ca-looping
Self-reactivation
CO2 capture
Ca-looping
Self-reactivation
spellingShingle CO2 capture
Ca-looping
Self-reactivation
CO2 capture
Ca-looping
Self-reactivation
Arias Rozada, Borja
Abanades García, Juan Carlos
Anthony, Edward J.
Model for self-reactivation of highly sintered CaO particles during CO2 capture looping cycles
description [EN] Calcium looping is an emerging high-temperature, energy-efficient, CO2 capture technology using CaO as a regenerable sorbent of CO2 through the reversible carbonation/calcination reaction. The stability of the sorbent plays a key role in the design of these systems. This paper revisits the self-reactivation phenomenon that has been reported for some highly deactivated CaO materials when submitted to repeated carbonation/calcination cycles under certain conditions. Self-reactivation is modelled in this paper as the result of a dynamic balance between the loss of activity in one cycle and the accumulated gain of activity by extended carbonation times, due to a product layer of CaCO3 that keeps building up on all surfaces, controlled by the slow diffusion of CO2. The model describes reasonably well the trends observed for some limestones and conditions. For other limestones and conditions, the carbonation mechanism is more complex and the model does not fit the evolution of the maximum Ca conversion with the number of cycles as well, although the general patterns of selfreactivation are still well reproduced.
format artículo
topic_facet CO2 capture
Ca-looping
Self-reactivation
author Arias Rozada, Borja
Abanades García, Juan Carlos
Anthony, Edward J.
author_facet Arias Rozada, Borja
Abanades García, Juan Carlos
Anthony, Edward J.
author_sort Arias Rozada, Borja
title Model for self-reactivation of highly sintered CaO particles during CO2 capture looping cycles
title_short Model for self-reactivation of highly sintered CaO particles during CO2 capture looping cycles
title_full Model for self-reactivation of highly sintered CaO particles during CO2 capture looping cycles
title_fullStr Model for self-reactivation of highly sintered CaO particles during CO2 capture looping cycles
title_full_unstemmed Model for self-reactivation of highly sintered CaO particles during CO2 capture looping cycles
title_sort model for self-reactivation of highly sintered cao particles during co2 capture looping cycles
publisher American Chemical Society
publishDate 2011-03-10
url http://hdl.handle.net/10261/40626
work_keys_str_mv AT ariasrozadaborja modelforselfreactivationofhighlysinteredcaoparticlesduringco2captureloopingcycles
AT abanadesgarciajuancarlos modelforselfreactivationofhighlysinteredcaoparticlesduringco2captureloopingcycles
AT anthonyedwardj modelforselfreactivationofhighlysinteredcaoparticlesduringco2captureloopingcycles
_version_ 1777668883151323136