Catalytic and Noncatalytic Wet Oxidation of Formaldehyde. A Novel Kinetic Model

Detalhes bibliográficos
Autor(a) principal: Silva, Adrián M. T.
Data de Publicação: 2003
Outros Autores: Quinta-Ferreira, Rosa M., Levec, Janez
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/10587
https://doi.org/10.1021/ie030090r
Resumo: Formaldehyde is a carcinogen compound and one of the most important pollutants contained in wastewaters. Three different treatments were evaluated in a high-pressure batch reactor for the total organic carbon (TOC) degradation of formaldehyde solutions: thermolysis, noncatalytic wet oxidation, and catalytic wet oxidation over a CuO−ZnO/Al2O3 catalyst. The absence of the catalyst leads to a predominant induction period (30 min) without changes in TOC concentrations, while the catalytic treatment leads to significant enhancement in TOC reduction. In the catalytic experiments, an asymptotic behavior was observed with a final TOC reduction of approximately 80%, with the remaining nonoxidizable TOC being due to methanol, a refractory compound contained in the formaldehyde solution that is resistant to oxidation even with increasing temperature and pressure. Formic acid was identified as an intermediary compound, and a new kinetic model was developed, designed as the modified generalized kinetic model, to account for refractory and nonoxidizable compounds. Moreover, leaching of the catalyst in the liquid phase was not significant, and the carbon adsorption capacity was not detected.
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spelling Catalytic and Noncatalytic Wet Oxidation of Formaldehyde. A Novel Kinetic ModelFormaldehyde is a carcinogen compound and one of the most important pollutants contained in wastewaters. Three different treatments were evaluated in a high-pressure batch reactor for the total organic carbon (TOC) degradation of formaldehyde solutions: thermolysis, noncatalytic wet oxidation, and catalytic wet oxidation over a CuO−ZnO/Al2O3 catalyst. The absence of the catalyst leads to a predominant induction period (30 min) without changes in TOC concentrations, while the catalytic treatment leads to significant enhancement in TOC reduction. In the catalytic experiments, an asymptotic behavior was observed with a final TOC reduction of approximately 80%, with the remaining nonoxidizable TOC being due to methanol, a refractory compound contained in the formaldehyde solution that is resistant to oxidation even with increasing temperature and pressure. Formic acid was identified as an intermediary compound, and a new kinetic model was developed, designed as the modified generalized kinetic model, to account for refractory and nonoxidizable compounds. Moreover, leaching of the catalyst in the liquid phase was not significant, and the carbon adsorption capacity was not detected.American Chemical Society2003-10-15info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/10587http://hdl.handle.net/10316/10587https://doi.org/10.1021/ie030090rengIndustrial & Engineering Chemistry Research. 42:21 (2003) 5099-51080888-5885Silva, Adrián M. T.Quinta-Ferreira, Rosa M.Levec, Janezinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2020-05-29T09:42:38Zoai:estudogeral.uc.pt:10316/10587Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:59:20.069719Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Catalytic and Noncatalytic Wet Oxidation of Formaldehyde. A Novel Kinetic Model
title Catalytic and Noncatalytic Wet Oxidation of Formaldehyde. A Novel Kinetic Model
spellingShingle Catalytic and Noncatalytic Wet Oxidation of Formaldehyde. A Novel Kinetic Model
Silva, Adrián M. T.
title_short Catalytic and Noncatalytic Wet Oxidation of Formaldehyde. A Novel Kinetic Model
title_full Catalytic and Noncatalytic Wet Oxidation of Formaldehyde. A Novel Kinetic Model
title_fullStr Catalytic and Noncatalytic Wet Oxidation of Formaldehyde. A Novel Kinetic Model
title_full_unstemmed Catalytic and Noncatalytic Wet Oxidation of Formaldehyde. A Novel Kinetic Model
title_sort Catalytic and Noncatalytic Wet Oxidation of Formaldehyde. A Novel Kinetic Model
author Silva, Adrián M. T.
author_facet Silva, Adrián M. T.
Quinta-Ferreira, Rosa M.
Levec, Janez
author_role author
author2 Quinta-Ferreira, Rosa M.
Levec, Janez
author2_role author
author
dc.contributor.author.fl_str_mv Silva, Adrián M. T.
Quinta-Ferreira, Rosa M.
Levec, Janez
description Formaldehyde is a carcinogen compound and one of the most important pollutants contained in wastewaters. Three different treatments were evaluated in a high-pressure batch reactor for the total organic carbon (TOC) degradation of formaldehyde solutions: thermolysis, noncatalytic wet oxidation, and catalytic wet oxidation over a CuO−ZnO/Al2O3 catalyst. The absence of the catalyst leads to a predominant induction period (30 min) without changes in TOC concentrations, while the catalytic treatment leads to significant enhancement in TOC reduction. In the catalytic experiments, an asymptotic behavior was observed with a final TOC reduction of approximately 80%, with the remaining nonoxidizable TOC being due to methanol, a refractory compound contained in the formaldehyde solution that is resistant to oxidation even with increasing temperature and pressure. Formic acid was identified as an intermediary compound, and a new kinetic model was developed, designed as the modified generalized kinetic model, to account for refractory and nonoxidizable compounds. Moreover, leaching of the catalyst in the liquid phase was not significant, and the carbon adsorption capacity was not detected.
publishDate 2003
dc.date.none.fl_str_mv 2003-10-15
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/10587
http://hdl.handle.net/10316/10587
https://doi.org/10.1021/ie030090r
url http://hdl.handle.net/10316/10587
https://doi.org/10.1021/ie030090r
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Industrial & Engineering Chemistry Research. 42:21 (2003) 5099-5108
0888-5885
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.publisher.none.fl_str_mv American Chemical Society
publisher.none.fl_str_mv American Chemical Society
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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