SYNERGIC EXTRACTION OF PANTOTHENIC ACID WITH TWO DIFFERENT EXTRACTANTS
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , |
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=S0104-66322016000401031 |
Resumo: | Abstract The influences of extractants concentrations and solvent polarity on the efficiency of pantothenic acid separation by synergic extraction with tri-n-octylamine (TOA) and di(2-ethylhexyl) phosphoric acid (D2EHPA) mixture have been analyzed. The results indicated the formation of an interfacial compound which includes one molecule of pantothenic acid and one of D2EHPA, its hydrophobicity being increased by solvation with additional TOA molecules. For solvents with lower dielectric constants, n-heptane and n-butyl acetate, the number of amine molecules participating in the interfacial complex formation was controlled by solvent polarity and D2EHPA concentration, decreasing with the increase of these two parameters. For dichloromethane, the chemical structure of the extracted compound remained the same regardless of D2EHPA concentration. The most important synergic effect corresponded to the extractant mixture dissolved in n-heptane, at low D2EHPA concentration in the organic phase (5 g/l). |
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oai:scielo:S0104-66322016000401031 |
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Brazilian Journal of Chemical Engineering |
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|
spelling |
SYNERGIC EXTRACTION OF PANTOTHENIC ACID WITH TWO DIFFERENT EXTRACTANTSPantothenic acidTri-n-octylamineDi(2-ethylhexyl) phosphoric acidSynergic extractionSynergistic coefficientDistribution coefficientAbstract The influences of extractants concentrations and solvent polarity on the efficiency of pantothenic acid separation by synergic extraction with tri-n-octylamine (TOA) and di(2-ethylhexyl) phosphoric acid (D2EHPA) mixture have been analyzed. The results indicated the formation of an interfacial compound which includes one molecule of pantothenic acid and one of D2EHPA, its hydrophobicity being increased by solvation with additional TOA molecules. For solvents with lower dielectric constants, n-heptane and n-butyl acetate, the number of amine molecules participating in the interfacial complex formation was controlled by solvent polarity and D2EHPA concentration, decreasing with the increase of these two parameters. For dichloromethane, the chemical structure of the extracted compound remained the same regardless of D2EHPA concentration. The most important synergic effect corresponded to the extractant mixture dissolved in n-heptane, at low D2EHPA concentration in the organic phase (5 g/l).Brazilian Society of Chemical Engineering2016-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66322016000401031Brazilian Journal of Chemical Engineering v.33 n.4 2016reponame:Brazilian Journal of Chemical Engineeringinstname:Associação Brasileira de Engenharia Química (ABEQ)instacron:ABEQ10.1590/0104-6632.20160334s20150265info:eu-repo/semantics/openAccessGalaction,A.-I.Poştaru,M.Bompa,A.-S.Caşcaval,D.eng2017-03-13T00:00:00Zoai:scielo:S0104-66322016000401031Revistahttps://www.scielo.br/j/bjce/https://old.scielo.br/oai/scielo-oai.phprgiudici@usp.br||rgiudici@usp.br1678-43830104-6632opendoar:2017-03-13T00:00Brazilian Journal of Chemical Engineering - Associação Brasileira de Engenharia Química (ABEQ)false |
dc.title.none.fl_str_mv |
SYNERGIC EXTRACTION OF PANTOTHENIC ACID WITH TWO DIFFERENT EXTRACTANTS |
title |
SYNERGIC EXTRACTION OF PANTOTHENIC ACID WITH TWO DIFFERENT EXTRACTANTS |
spellingShingle |
SYNERGIC EXTRACTION OF PANTOTHENIC ACID WITH TWO DIFFERENT EXTRACTANTS Galaction,A.-I. Pantothenic acid Tri-n-octylamine Di(2-ethylhexyl) phosphoric acid Synergic extraction Synergistic coefficient Distribution coefficient |
title_short |
SYNERGIC EXTRACTION OF PANTOTHENIC ACID WITH TWO DIFFERENT EXTRACTANTS |
title_full |
SYNERGIC EXTRACTION OF PANTOTHENIC ACID WITH TWO DIFFERENT EXTRACTANTS |
title_fullStr |
SYNERGIC EXTRACTION OF PANTOTHENIC ACID WITH TWO DIFFERENT EXTRACTANTS |
title_full_unstemmed |
SYNERGIC EXTRACTION OF PANTOTHENIC ACID WITH TWO DIFFERENT EXTRACTANTS |
title_sort |
SYNERGIC EXTRACTION OF PANTOTHENIC ACID WITH TWO DIFFERENT EXTRACTANTS |
author |
Galaction,A.-I. |
author_facet |
Galaction,A.-I. Poştaru,M. Bompa,A.-S. Caşcaval,D. |
author_role |
author |
author2 |
Poştaru,M. Bompa,A.-S. Caşcaval,D. |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Galaction,A.-I. Poştaru,M. Bompa,A.-S. Caşcaval,D. |
dc.subject.por.fl_str_mv |
Pantothenic acid Tri-n-octylamine Di(2-ethylhexyl) phosphoric acid Synergic extraction Synergistic coefficient Distribution coefficient |
topic |
Pantothenic acid Tri-n-octylamine Di(2-ethylhexyl) phosphoric acid Synergic extraction Synergistic coefficient Distribution coefficient |
description |
Abstract The influences of extractants concentrations and solvent polarity on the efficiency of pantothenic acid separation by synergic extraction with tri-n-octylamine (TOA) and di(2-ethylhexyl) phosphoric acid (D2EHPA) mixture have been analyzed. The results indicated the formation of an interfacial compound which includes one molecule of pantothenic acid and one of D2EHPA, its hydrophobicity being increased by solvation with additional TOA molecules. For solvents with lower dielectric constants, n-heptane and n-butyl acetate, the number of amine molecules participating in the interfacial complex formation was controlled by solvent polarity and D2EHPA concentration, decreasing with the increase of these two parameters. For dichloromethane, the chemical structure of the extracted compound remained the same regardless of D2EHPA concentration. The most important synergic effect corresponded to the extractant mixture dissolved in n-heptane, at low D2EHPA concentration in the organic phase (5 g/l). |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016-12-01 |
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=S0104-66322016000401031 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66322016000401031 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/0104-6632.20160334s20150265 |
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.4 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 |
_version_ |
1754213175420518400 |