The removal of dinitrochlorobenzene from industrial residuals by liquid-liquid extraction with chemical reaction

Detalhes bibliográficos
Autor(a) principal: Ferreira,G. C. M.
Data de Publicação: 2007
Outros Autores: Góis,L. M. N., Lobo,W.
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=S0104-66322007000300014
Resumo: Nitrochlorobenzenes (NCBs) are very important in the chemical industry since they have been used as raw material for the manufacture of crop protection products, as active ingredients in the pharmaceutical industry, as pigments and as antioxidants as well as for other uses. In industrial processes, NCBs are produced by monochlorobenzene (MCB) nitration reactions and one of the main residuals formed is dinitrochlorobenzene (DNCB), which is mainly composed of the isomer 2,4DNCB. This subproduct, although of commercial interest when in its pure state, is generally incinerated due to the high costs of recovery treatment and purification. The objective of this study is to present an alternative to the treatment of industrial residuals containing DNCB. The technique consists of converting DNCB into sodium dinitrophenolate, which is very soluble in water and is also easy to reuse. For this purpose, liquid-liquid extraction with chemical reaction (alkaline hydrolysis) with a rotating disc contactor (RDC) is used. Experimental data on MCB nitration reactions as well as alkaline hydrolysis using a rotating disc contactor are presented.
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spelling The removal of dinitrochlorobenzene from industrial residuals by liquid-liquid extraction with chemical reactionExtractionReactionDinitrochlorobenzeneNitrochlorobenzenes (NCBs) are very important in the chemical industry since they have been used as raw material for the manufacture of crop protection products, as active ingredients in the pharmaceutical industry, as pigments and as antioxidants as well as for other uses. In industrial processes, NCBs are produced by monochlorobenzene (MCB) nitration reactions and one of the main residuals formed is dinitrochlorobenzene (DNCB), which is mainly composed of the isomer 2,4DNCB. This subproduct, although of commercial interest when in its pure state, is generally incinerated due to the high costs of recovery treatment and purification. The objective of this study is to present an alternative to the treatment of industrial residuals containing DNCB. The technique consists of converting DNCB into sodium dinitrophenolate, which is very soluble in water and is also easy to reuse. For this purpose, liquid-liquid extraction with chemical reaction (alkaline hydrolysis) with a rotating disc contactor (RDC) is used. Experimental data on MCB nitration reactions as well as alkaline hydrolysis using a rotating disc contactor are presented.Brazilian Society of Chemical Engineering2007-09-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66322007000300014Brazilian Journal of Chemical Engineering v.24 n.3 2007reponame:Brazilian Journal of Chemical Engineeringinstname:Associação Brasileira de Engenharia Química (ABEQ)instacron:ABEQ10.1590/S0104-66322007000300014info:eu-repo/semantics/openAccessFerreira,G. C. M.Góis,L. M. N.Lobo,W.eng2007-11-23T00:00:00Zoai:scielo:S0104-66322007000300014Revistahttps://www.scielo.br/j/bjce/https://old.scielo.br/oai/scielo-oai.phprgiudici@usp.br||rgiudici@usp.br1678-43830104-6632opendoar:2007-11-23T00:00Brazilian Journal of Chemical Engineering - Associação Brasileira de Engenharia Química (ABEQ)false
dc.title.none.fl_str_mv The removal of dinitrochlorobenzene from industrial residuals by liquid-liquid extraction with chemical reaction
title The removal of dinitrochlorobenzene from industrial residuals by liquid-liquid extraction with chemical reaction
spellingShingle The removal of dinitrochlorobenzene from industrial residuals by liquid-liquid extraction with chemical reaction
Ferreira,G. C. M.
Extraction
Reaction
Dinitrochlorobenzene
title_short The removal of dinitrochlorobenzene from industrial residuals by liquid-liquid extraction with chemical reaction
title_full The removal of dinitrochlorobenzene from industrial residuals by liquid-liquid extraction with chemical reaction
title_fullStr The removal of dinitrochlorobenzene from industrial residuals by liquid-liquid extraction with chemical reaction
title_full_unstemmed The removal of dinitrochlorobenzene from industrial residuals by liquid-liquid extraction with chemical reaction
title_sort The removal of dinitrochlorobenzene from industrial residuals by liquid-liquid extraction with chemical reaction
author Ferreira,G. C. M.
author_facet Ferreira,G. C. M.
Góis,L. M. N.
Lobo,W.
author_role author
author2 Góis,L. M. N.
Lobo,W.
author2_role author
author
dc.contributor.author.fl_str_mv Ferreira,G. C. M.
Góis,L. M. N.
Lobo,W.
dc.subject.por.fl_str_mv Extraction
Reaction
Dinitrochlorobenzene
topic Extraction
Reaction
Dinitrochlorobenzene
description Nitrochlorobenzenes (NCBs) are very important in the chemical industry since they have been used as raw material for the manufacture of crop protection products, as active ingredients in the pharmaceutical industry, as pigments and as antioxidants as well as for other uses. In industrial processes, NCBs are produced by monochlorobenzene (MCB) nitration reactions and one of the main residuals formed is dinitrochlorobenzene (DNCB), which is mainly composed of the isomer 2,4DNCB. This subproduct, although of commercial interest when in its pure state, is generally incinerated due to the high costs of recovery treatment and purification. The objective of this study is to present an alternative to the treatment of industrial residuals containing DNCB. The technique consists of converting DNCB into sodium dinitrophenolate, which is very soluble in water and is also easy to reuse. For this purpose, liquid-liquid extraction with chemical reaction (alkaline hydrolysis) with a rotating disc contactor (RDC) is used. Experimental data on MCB nitration reactions as well as alkaline hydrolysis using a rotating disc contactor are presented.
publishDate 2007
dc.date.none.fl_str_mv 2007-09-01
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=S0104-66322007000300014
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66322007000300014
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0104-66322007000300014
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.24 n.3 2007
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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