Electrochemical degradation of the reactive red 141 dye on a β-PbO2 anode assessed by the response surface methodology

Detalhes bibliográficos
Autor(a) principal: Aquino,José M.
Data de Publicação: 2010
Outros Autores: Rocha-Filho,Romeu C., Bocchi,Nerilso, Biaggio,Sonia R.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532010000200019
Resumo: The electrochemical degradation of the Reactive Red 141 dye using a filter-press reactor with a β-PbO2 anode was investigated through the application of the response surface methodology. The charge required for 90% decolorization (Q90) and the chemical oxygen demand removal percentage after 30 min electrolysis (COD30) were used to model the system. The investigated independent variables were the current density, pH, NaCl concentration, and temperature. Low values of Q90 (0.2-0.3 A h L-1) were obtained at acidic conditions (pH 1-3) and high concentrations of NaCl (1.0-2.0 g L-1), when Cl2 and HOCl are the predominant oxidant species. The best values of COD30 were obtained at high current densities and acidic to neutral conditions (pH 5-7); however, the consequent energy consumption makes the process not economically feasible under these conditions. For strongly acidic solutions, specific energy consumptions associated to Q90 as low as 0.79 kW h m-3 were attained.
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spelling Electrochemical degradation of the reactive red 141 dye on a β-PbO2 anode assessed by the response surface methodologyelectrooxidationdye degradationReactive-Red 141 dyePbO2 anodefactorial designThe electrochemical degradation of the Reactive Red 141 dye using a filter-press reactor with a β-PbO2 anode was investigated through the application of the response surface methodology. The charge required for 90% decolorization (Q90) and the chemical oxygen demand removal percentage after 30 min electrolysis (COD30) were used to model the system. The investigated independent variables were the current density, pH, NaCl concentration, and temperature. Low values of Q90 (0.2-0.3 A h L-1) were obtained at acidic conditions (pH 1-3) and high concentrations of NaCl (1.0-2.0 g L-1), when Cl2 and HOCl are the predominant oxidant species. The best values of COD30 were obtained at high current densities and acidic to neutral conditions (pH 5-7); however, the consequent energy consumption makes the process not economically feasible under these conditions. For strongly acidic solutions, specific energy consumptions associated to Q90 as low as 0.79 kW h m-3 were attained.Sociedade Brasileira de Química2010-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532010000200019Journal of the Brazilian Chemical Society v.21 n.2 2010reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532010000200019info:eu-repo/semantics/openAccessAquino,José M.Rocha-Filho,Romeu C.Bocchi,NerilsoBiaggio,Sonia R.eng2010-03-17T00:00:00Zoai:scielo:S0103-50532010000200019Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2010-03-17T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Electrochemical degradation of the reactive red 141 dye on a β-PbO2 anode assessed by the response surface methodology
title Electrochemical degradation of the reactive red 141 dye on a β-PbO2 anode assessed by the response surface methodology
spellingShingle Electrochemical degradation of the reactive red 141 dye on a β-PbO2 anode assessed by the response surface methodology
Aquino,José M.
electrooxidation
dye degradation
Reactive-Red 141 dye
PbO2 anode
factorial design
title_short Electrochemical degradation of the reactive red 141 dye on a β-PbO2 anode assessed by the response surface methodology
title_full Electrochemical degradation of the reactive red 141 dye on a β-PbO2 anode assessed by the response surface methodology
title_fullStr Electrochemical degradation of the reactive red 141 dye on a β-PbO2 anode assessed by the response surface methodology
title_full_unstemmed Electrochemical degradation of the reactive red 141 dye on a β-PbO2 anode assessed by the response surface methodology
title_sort Electrochemical degradation of the reactive red 141 dye on a β-PbO2 anode assessed by the response surface methodology
author Aquino,José M.
author_facet Aquino,José M.
Rocha-Filho,Romeu C.
Bocchi,Nerilso
Biaggio,Sonia R.
author_role author
author2 Rocha-Filho,Romeu C.
Bocchi,Nerilso
Biaggio,Sonia R.
author2_role author
author
author
dc.contributor.author.fl_str_mv Aquino,José M.
Rocha-Filho,Romeu C.
Bocchi,Nerilso
Biaggio,Sonia R.
dc.subject.por.fl_str_mv electrooxidation
dye degradation
Reactive-Red 141 dye
PbO2 anode
factorial design
topic electrooxidation
dye degradation
Reactive-Red 141 dye
PbO2 anode
factorial design
description The electrochemical degradation of the Reactive Red 141 dye using a filter-press reactor with a β-PbO2 anode was investigated through the application of the response surface methodology. The charge required for 90% decolorization (Q90) and the chemical oxygen demand removal percentage after 30 min electrolysis (COD30) were used to model the system. The investigated independent variables were the current density, pH, NaCl concentration, and temperature. Low values of Q90 (0.2-0.3 A h L-1) were obtained at acidic conditions (pH 1-3) and high concentrations of NaCl (1.0-2.0 g L-1), when Cl2 and HOCl are the predominant oxidant species. The best values of COD30 were obtained at high current densities and acidic to neutral conditions (pH 5-7); however, the consequent energy consumption makes the process not economically feasible under these conditions. For strongly acidic solutions, specific energy consumptions associated to Q90 as low as 0.79 kW h m-3 were attained.
publishDate 2010
dc.date.none.fl_str_mv 2010-01-01
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=S0103-50532010000200019
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532010000200019
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532010000200019
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 Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.21 n.2 2010
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
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