Relative lability of trace metals complexed in aquatic humic substances using ion-exchanger cellulose-hyphan

Bibliographic Details
Main Author: Rocha, Julio Cesar [UNESP]
Publication Date: 1997
Other Authors: Toscano, Ilda A. S. [UNESP], Cardoso, Arnaldo Alves [UNESP]
Format: Article
Language: eng
Source: Repositório Institucional da UNESP
Download full: http://dx.doi.org/10.1590/S0103-50531997000300010
http://hdl.handle.net/11449/65294
Summary: The purpose of this paper is to characterize the lability/inertness metal fractions complexed by aquatic humic substances (HS) in relation to pH, complexation time, and HS concentration. HS were preconcentrated by ultrafiltration and complexed with bivalent metal ions. These fractions were characterized by ion exchange with the chelating collector cellulose Hyphan by applying batch procedure. The metals were determined by atomic absorption spectrometry. The results show that the distribution coefficients, Kd, decreased with HS presence, and that the relative lability of metal fractions complexed by HS is dependent on variables such as pH, complexation time, and HS concentration. Until c.a. 15 min, the metal change between aquatic HS and ion exchanger occurs following a 2 order reaction. Afterwards, the remaining metal fraction in the HS reacts following a 1st order reaction. For traces of metal ions bound to dissolved HS, the lability orderPb > Mn > Cd, Ni > Cu is revealed. ©1997 Soc. Bras. Química.
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spelling Relative lability of trace metals complexed in aquatic humic substances using ion-exchanger cellulose-hyphanAquatic humic substancesIon-exchangeMetal complexationThe purpose of this paper is to characterize the lability/inertness metal fractions complexed by aquatic humic substances (HS) in relation to pH, complexation time, and HS concentration. HS were preconcentrated by ultrafiltration and complexed with bivalent metal ions. These fractions were characterized by ion exchange with the chelating collector cellulose Hyphan by applying batch procedure. The metals were determined by atomic absorption spectrometry. The results show that the distribution coefficients, Kd, decreased with HS presence, and that the relative lability of metal fractions complexed by HS is dependent on variables such as pH, complexation time, and HS concentration. Until c.a. 15 min, the metal change between aquatic HS and ion exchanger occurs following a 2 order reaction. Afterwards, the remaining metal fraction in the HS reacts following a 1st order reaction. For traces of metal ions bound to dissolved HS, the lability orderPb > Mn > Cd, Ni > Cu is revealed. ©1997 Soc. Bras. Química.Depto. de Quim. Analítica Inst. de Quim. de Araraquara- UNESP, C.P. 355, 14800-900 Araraquara - SPDepto. de Quim. Analítica Inst. de Quim. de Araraquara- UNESP, C.P. 355, 14800-900 Araraquara - SPUniversidade Estadual Paulista (Unesp)Rocha, Julio Cesar [UNESP]Toscano, Ilda A. S. [UNESP]Cardoso, Arnaldo Alves [UNESP]2014-05-27T11:18:18Z2014-05-27T11:18:18Z1997-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article239-243application/pdfhttp://dx.doi.org/10.1590/S0103-50531997000300010Journal of the Brazilian Chemical Society, v. 8, n. 3, p. 239-243, 1997.0103-5053http://hdl.handle.net/11449/6529410.1590/S0103-50531997000300010S0103-50531997000300010WOS:A1997XG435000102-s2.0-188444451442-s2.0-18844445144.pdf41488374036182079165109840414837Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of the Brazilian Chemical Society1.4440,357info:eu-repo/semantics/openAccess2023-11-08T06:10:46Zoai:repositorio.unesp.br:11449/65294Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-11-08T06:10:46Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Relative lability of trace metals complexed in aquatic humic substances using ion-exchanger cellulose-hyphan
title Relative lability of trace metals complexed in aquatic humic substances using ion-exchanger cellulose-hyphan
spellingShingle Relative lability of trace metals complexed in aquatic humic substances using ion-exchanger cellulose-hyphan
Rocha, Julio Cesar [UNESP]
Aquatic humic substances
Ion-exchange
Metal complexation
title_short Relative lability of trace metals complexed in aquatic humic substances using ion-exchanger cellulose-hyphan
title_full Relative lability of trace metals complexed in aquatic humic substances using ion-exchanger cellulose-hyphan
title_fullStr Relative lability of trace metals complexed in aquatic humic substances using ion-exchanger cellulose-hyphan
title_full_unstemmed Relative lability of trace metals complexed in aquatic humic substances using ion-exchanger cellulose-hyphan
title_sort Relative lability of trace metals complexed in aquatic humic substances using ion-exchanger cellulose-hyphan
author Rocha, Julio Cesar [UNESP]
author_facet Rocha, Julio Cesar [UNESP]
Toscano, Ilda A. S. [UNESP]
Cardoso, Arnaldo Alves [UNESP]
author_role author
author2 Toscano, Ilda A. S. [UNESP]
Cardoso, Arnaldo Alves [UNESP]
author2_role author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Rocha, Julio Cesar [UNESP]
Toscano, Ilda A. S. [UNESP]
Cardoso, Arnaldo Alves [UNESP]
dc.subject.por.fl_str_mv Aquatic humic substances
Ion-exchange
Metal complexation
topic Aquatic humic substances
Ion-exchange
Metal complexation
description The purpose of this paper is to characterize the lability/inertness metal fractions complexed by aquatic humic substances (HS) in relation to pH, complexation time, and HS concentration. HS were preconcentrated by ultrafiltration and complexed with bivalent metal ions. These fractions were characterized by ion exchange with the chelating collector cellulose Hyphan by applying batch procedure. The metals were determined by atomic absorption spectrometry. The results show that the distribution coefficients, Kd, decreased with HS presence, and that the relative lability of metal fractions complexed by HS is dependent on variables such as pH, complexation time, and HS concentration. Until c.a. 15 min, the metal change between aquatic HS and ion exchanger occurs following a 2 order reaction. Afterwards, the remaining metal fraction in the HS reacts following a 1st order reaction. For traces of metal ions bound to dissolved HS, the lability orderPb > Mn > Cd, Ni > Cu is revealed. ©1997 Soc. Bras. Química.
publishDate 1997
dc.date.none.fl_str_mv 1997-12-01
2014-05-27T11:18:18Z
2014-05-27T11:18:18Z
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://dx.doi.org/10.1590/S0103-50531997000300010
Journal of the Brazilian Chemical Society, v. 8, n. 3, p. 239-243, 1997.
0103-5053
http://hdl.handle.net/11449/65294
10.1590/S0103-50531997000300010
S0103-50531997000300010
WOS:A1997XG43500010
2-s2.0-18844445144
2-s2.0-18844445144.pdf
4148837403618207
9165109840414837
url http://dx.doi.org/10.1590/S0103-50531997000300010
http://hdl.handle.net/11449/65294
identifier_str_mv Journal of the Brazilian Chemical Society, v. 8, n. 3, p. 239-243, 1997.
0103-5053
10.1590/S0103-50531997000300010
S0103-50531997000300010
WOS:A1997XG43500010
2-s2.0-18844445144
2-s2.0-18844445144.pdf
4148837403618207
9165109840414837
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of the Brazilian Chemical Society
1.444
0,357
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 239-243
application/pdf
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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