Development of sequential injection methodologies for the spectrophotometric direct and kinetic determination of aluminium in natural and waste waters
Autor(a) principal: | |
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Data de Publicação: | 2008 |
Outros Autores: | |
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=S0103-50532008000600018 |
Resumo: | Two sequential injection methodologies for the spectrophotometric determination of reactive aluminium in water samples are proposed, based on the reaction between chrome azurol S (CAS) and aluminium. The two methods involve a direct and a kinetic methodology (for its application to coloured waste waters), both accommodated within the same manifold. The working ranges obtained were: 0.040-0.500 mg Al L-1 for direct method and 0.050-0.300 mg Al L-1 for the kinetic method. The described system has high degree of automation, enabling sampling throughputs of 31 and 57 h-1 for the kinetic method and direct methods, respectively. The reagents consumption per determination is low: 46 µg of CAS, 3.75 mg of sodium acetate and 25 µg of ascorbic acid. The volume of effluent produced per determination is only around 2.8 mL in the direct method and 3.4 mL in the kinetic method. |
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Development of sequential injection methodologies for the spectrophotometric direct and kinetic determination of aluminium in natural and waste waterssequential injectionspectrophotometryaluminiumwaterskinetic determinationTwo sequential injection methodologies for the spectrophotometric determination of reactive aluminium in water samples are proposed, based on the reaction between chrome azurol S (CAS) and aluminium. The two methods involve a direct and a kinetic methodology (for its application to coloured waste waters), both accommodated within the same manifold. The working ranges obtained were: 0.040-0.500 mg Al L-1 for direct method and 0.050-0.300 mg Al L-1 for the kinetic method. The described system has high degree of automation, enabling sampling throughputs of 31 and 57 h-1 for the kinetic method and direct methods, respectively. The reagents consumption per determination is low: 46 µg of CAS, 3.75 mg of sodium acetate and 25 µg of ascorbic acid. The volume of effluent produced per determination is only around 2.8 mL in the direct method and 3.4 mL in the kinetic method.Sociedade Brasileira de Química2008-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532008000600018Journal of the Brazilian Chemical Society v.19 n.6 2008reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532008000600018info:eu-repo/semantics/openAccessMesquita,Raquel B. R.Rangel,António O. S. S.eng2008-09-15T00:00:00Zoai:scielo:S0103-50532008000600018Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2008-09-15T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Development of sequential injection methodologies for the spectrophotometric direct and kinetic determination of aluminium in natural and waste waters |
title |
Development of sequential injection methodologies for the spectrophotometric direct and kinetic determination of aluminium in natural and waste waters |
spellingShingle |
Development of sequential injection methodologies for the spectrophotometric direct and kinetic determination of aluminium in natural and waste waters Mesquita,Raquel B. R. sequential injection spectrophotometry aluminium waters kinetic determination |
title_short |
Development of sequential injection methodologies for the spectrophotometric direct and kinetic determination of aluminium in natural and waste waters |
title_full |
Development of sequential injection methodologies for the spectrophotometric direct and kinetic determination of aluminium in natural and waste waters |
title_fullStr |
Development of sequential injection methodologies for the spectrophotometric direct and kinetic determination of aluminium in natural and waste waters |
title_full_unstemmed |
Development of sequential injection methodologies for the spectrophotometric direct and kinetic determination of aluminium in natural and waste waters |
title_sort |
Development of sequential injection methodologies for the spectrophotometric direct and kinetic determination of aluminium in natural and waste waters |
author |
Mesquita,Raquel B. R. |
author_facet |
Mesquita,Raquel B. R. Rangel,António O. S. S. |
author_role |
author |
author2 |
Rangel,António O. S. S. |
author2_role |
author |
dc.contributor.author.fl_str_mv |
Mesquita,Raquel B. R. Rangel,António O. S. S. |
dc.subject.por.fl_str_mv |
sequential injection spectrophotometry aluminium waters kinetic determination |
topic |
sequential injection spectrophotometry aluminium waters kinetic determination |
description |
Two sequential injection methodologies for the spectrophotometric determination of reactive aluminium in water samples are proposed, based on the reaction between chrome azurol S (CAS) and aluminium. The two methods involve a direct and a kinetic methodology (for its application to coloured waste waters), both accommodated within the same manifold. The working ranges obtained were: 0.040-0.500 mg Al L-1 for direct method and 0.050-0.300 mg Al L-1 for the kinetic method. The described system has high degree of automation, enabling sampling throughputs of 31 and 57 h-1 for the kinetic method and direct methods, respectively. The reagents consumption per determination is low: 46 µg of CAS, 3.75 mg of sodium acetate and 25 µg of ascorbic acid. The volume of effluent produced per determination is only around 2.8 mL in the direct method and 3.4 mL in the kinetic method. |
publishDate |
2008 |
dc.date.none.fl_str_mv |
2008-01-01 |
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=S0103-50532008000600018 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532008000600018 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0103-50532008000600018 |
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.19 n.6 2008 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 |
_version_ |
1750318169060278272 |