THE USE OF A HIGH LIMESTONE CONTENT MINING WASTE AS A SORBENT FOR CO2 CAPTURE

Detalhes bibliográficos
Autor(a) principal: Barbosa,R. C.
Data de Publicação: 2016
Outros Autores: Damasceno,J. J. R., Hori,C. E.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Chemical Engineering
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66322016000300599
Resumo: Abstract In this work, a high limestone content waste was evaluated as a potential material for CO2 capture. The influence of calcination conditions on the CO2 capture capacity was evaluated using 5 cycles of calcination-hydration-carbonation reactions. A Central Composite Design of Experiments was set using calcination temperatures and time as variables. The response evaluated was the CO2 capture measured by thermogravimetric analysis. The results indicate that both calcination temperature and time influence the CO2 capture capacities in the initial cycles but, after a large number of cycles, the effect becomes less relevant. The optimum calcination temperature did not change significantly between cycles - about 893 °C in the first and 850 °C in the fourth cycle. However, the optimum calcination time decreased from 40.1 min in the first to 22.5 min in the fourth cycle. The maximum CO2 capture capacity declines over the reaction cycles due to the sorbent sintering, which becomes more noticeable. Moreover, the waste used in this work is suitable for separating CO2 from flue gas, achieving more than 0.2 g/g of capture capacity after five cycles.
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spelling THE USE OF A HIGH LIMESTONE CONTENT MINING WASTE AS A SORBENT FOR CO2 CAPTURECO2 captureLimestoneCalcium oxideCalcium carbonateAbstract In this work, a high limestone content waste was evaluated as a potential material for CO2 capture. The influence of calcination conditions on the CO2 capture capacity was evaluated using 5 cycles of calcination-hydration-carbonation reactions. A Central Composite Design of Experiments was set using calcination temperatures and time as variables. The response evaluated was the CO2 capture measured by thermogravimetric analysis. The results indicate that both calcination temperature and time influence the CO2 capture capacities in the initial cycles but, after a large number of cycles, the effect becomes less relevant. The optimum calcination temperature did not change significantly between cycles - about 893 °C in the first and 850 °C in the fourth cycle. However, the optimum calcination time decreased from 40.1 min in the first to 22.5 min in the fourth cycle. The maximum CO2 capture capacity declines over the reaction cycles due to the sorbent sintering, which becomes more noticeable. Moreover, the waste used in this work is suitable for separating CO2 from flue gas, achieving more than 0.2 g/g of capture capacity after five cycles.Brazilian Society of Chemical Engineering2016-09-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66322016000300599Brazilian Journal of Chemical Engineering v.33 n.3 2016reponame:Brazilian Journal of Chemical Engineeringinstname:Associação Brasileira de Engenharia Química (ABEQ)instacron:ABEQ10.1590/0104-6632.20160333s20150111info:eu-repo/semantics/openAccessBarbosa,R. C.Damasceno,J. J. R.Hori,C. E.eng2016-11-18T00:00:00Zoai:scielo:S0104-66322016000300599Revistahttps://www.scielo.br/j/bjce/https://old.scielo.br/oai/scielo-oai.phprgiudici@usp.br||rgiudici@usp.br1678-43830104-6632opendoar:2016-11-18T00:00Brazilian Journal of Chemical Engineering - Associação Brasileira de Engenharia Química (ABEQ)false
dc.title.none.fl_str_mv THE USE OF A HIGH LIMESTONE CONTENT MINING WASTE AS A SORBENT FOR CO2 CAPTURE
title THE USE OF A HIGH LIMESTONE CONTENT MINING WASTE AS A SORBENT FOR CO2 CAPTURE
spellingShingle THE USE OF A HIGH LIMESTONE CONTENT MINING WASTE AS A SORBENT FOR CO2 CAPTURE
Barbosa,R. C.
CO2 capture
Limestone
Calcium oxide
Calcium carbonate
title_short THE USE OF A HIGH LIMESTONE CONTENT MINING WASTE AS A SORBENT FOR CO2 CAPTURE
title_full THE USE OF A HIGH LIMESTONE CONTENT MINING WASTE AS A SORBENT FOR CO2 CAPTURE
title_fullStr THE USE OF A HIGH LIMESTONE CONTENT MINING WASTE AS A SORBENT FOR CO2 CAPTURE
title_full_unstemmed THE USE OF A HIGH LIMESTONE CONTENT MINING WASTE AS A SORBENT FOR CO2 CAPTURE
title_sort THE USE OF A HIGH LIMESTONE CONTENT MINING WASTE AS A SORBENT FOR CO2 CAPTURE
author Barbosa,R. C.
author_facet Barbosa,R. C.
Damasceno,J. J. R.
Hori,C. E.
author_role author
author2 Damasceno,J. J. R.
Hori,C. E.
author2_role author
author
dc.contributor.author.fl_str_mv Barbosa,R. C.
Damasceno,J. J. R.
Hori,C. E.
dc.subject.por.fl_str_mv CO2 capture
Limestone
Calcium oxide
Calcium carbonate
topic CO2 capture
Limestone
Calcium oxide
Calcium carbonate
description Abstract In this work, a high limestone content waste was evaluated as a potential material for CO2 capture. The influence of calcination conditions on the CO2 capture capacity was evaluated using 5 cycles of calcination-hydration-carbonation reactions. A Central Composite Design of Experiments was set using calcination temperatures and time as variables. The response evaluated was the CO2 capture measured by thermogravimetric analysis. The results indicate that both calcination temperature and time influence the CO2 capture capacities in the initial cycles but, after a large number of cycles, the effect becomes less relevant. The optimum calcination temperature did not change significantly between cycles - about 893 °C in the first and 850 °C in the fourth cycle. However, the optimum calcination time decreased from 40.1 min in the first to 22.5 min in the fourth cycle. The maximum CO2 capture capacity declines over the reaction cycles due to the sorbent sintering, which becomes more noticeable. Moreover, the waste used in this work is suitable for separating CO2 from flue gas, achieving more than 0.2 g/g of capture capacity after five cycles.
publishDate 2016
dc.date.none.fl_str_mv 2016-09-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66322016000300599
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66322016000300599
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/0104-6632.20160333s20150111
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Brazilian Society of Chemical Engineering
publisher.none.fl_str_mv Brazilian Society of Chemical Engineering
dc.source.none.fl_str_mv Brazilian Journal of Chemical Engineering v.33 n.3 2016
reponame:Brazilian Journal of Chemical Engineering
instname:Associação Brasileira de Engenharia Química (ABEQ)
instacron:ABEQ
instname_str Associação Brasileira de Engenharia Química (ABEQ)
instacron_str ABEQ
institution ABEQ
reponame_str Brazilian Journal of Chemical Engineering
collection Brazilian Journal of Chemical Engineering
repository.name.fl_str_mv Brazilian Journal of Chemical Engineering - Associação Brasileira de Engenharia Química (ABEQ)
repository.mail.fl_str_mv rgiudici@usp.br||rgiudici@usp.br
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