Development of a fluorimetric sequential injection analysis (SIA) methodology for determination of quinine
Autor(a) principal: | |
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Data de Publicação: | 2011 |
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=S0103-50532011001000009 |
Resumo: | A sequential injection analysis (SIA) methodology was developed for fluorimetric determination of quinine in soft drinks. Minimum dispersion and efficient mixing were achieved by aspirating 200 mL of sample between two 100 mL reagent zones (0.10 mol L-1 H2SO4) at flow rate of 250 mL s-1 and using a reaction coil length of 50 cm (0.8 mm internal diameter). Linear response for quinine concentrations (C) between 0.050 and 100.0 mg L-1 was described by: I = (532 ± 40) + (2.36 ± 0.04) C, with r = 0.999, where I is the relative fluorescence intensity. The coefficient of variation and limits of detection and quantification were 1.9% (0.50 mg L-1 n = 10), 2.3 and 4.5 mg L-1, respectively. The sampling throughput was 60 analyses per hour, consuming 2.2 mL of concentrated H2SO4 and producing 4 mL of wastes per analysis. No statistically significant differences were observed between the results obtained by the proposed SIA methodology and the ones obtained by the batch procedure. |
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Journal of the Brazilian Chemical Society (Online) |
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Development of a fluorimetric sequential injection analysis (SIA) methodology for determination of quininesequential injection analysisquininefluorimetrydispersionoptimizationA sequential injection analysis (SIA) methodology was developed for fluorimetric determination of quinine in soft drinks. Minimum dispersion and efficient mixing were achieved by aspirating 200 mL of sample between two 100 mL reagent zones (0.10 mol L-1 H2SO4) at flow rate of 250 mL s-1 and using a reaction coil length of 50 cm (0.8 mm internal diameter). Linear response for quinine concentrations (C) between 0.050 and 100.0 mg L-1 was described by: I = (532 ± 40) + (2.36 ± 0.04) C, with r = 0.999, where I is the relative fluorescence intensity. The coefficient of variation and limits of detection and quantification were 1.9% (0.50 mg L-1 n = 10), 2.3 and 4.5 mg L-1, respectively. The sampling throughput was 60 analyses per hour, consuming 2.2 mL of concentrated H2SO4 and producing 4 mL of wastes per analysis. No statistically significant differences were observed between the results obtained by the proposed SIA methodology and the ones obtained by the batch procedure.Sociedade Brasileira de Química2011-10-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532011001000009Journal of the Brazilian Chemical Society v.22 n.10 2011reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532011001000009info:eu-repo/semantics/openAccessInfante,Carlos M. C.Masini,Jorge C.eng2011-10-25T00:00:00Zoai:scielo:S0103-50532011001000009Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2011-10-25T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Development of a fluorimetric sequential injection analysis (SIA) methodology for determination of quinine |
title |
Development of a fluorimetric sequential injection analysis (SIA) methodology for determination of quinine |
spellingShingle |
Development of a fluorimetric sequential injection analysis (SIA) methodology for determination of quinine Infante,Carlos M. C. sequential injection analysis quinine fluorimetry dispersion optimization |
title_short |
Development of a fluorimetric sequential injection analysis (SIA) methodology for determination of quinine |
title_full |
Development of a fluorimetric sequential injection analysis (SIA) methodology for determination of quinine |
title_fullStr |
Development of a fluorimetric sequential injection analysis (SIA) methodology for determination of quinine |
title_full_unstemmed |
Development of a fluorimetric sequential injection analysis (SIA) methodology for determination of quinine |
title_sort |
Development of a fluorimetric sequential injection analysis (SIA) methodology for determination of quinine |
author |
Infante,Carlos M. C. |
author_facet |
Infante,Carlos M. C. Masini,Jorge C. |
author_role |
author |
author2 |
Masini,Jorge C. |
author2_role |
author |
dc.contributor.author.fl_str_mv |
Infante,Carlos M. C. Masini,Jorge C. |
dc.subject.por.fl_str_mv |
sequential injection analysis quinine fluorimetry dispersion optimization |
topic |
sequential injection analysis quinine fluorimetry dispersion optimization |
description |
A sequential injection analysis (SIA) methodology was developed for fluorimetric determination of quinine in soft drinks. Minimum dispersion and efficient mixing were achieved by aspirating 200 mL of sample between two 100 mL reagent zones (0.10 mol L-1 H2SO4) at flow rate of 250 mL s-1 and using a reaction coil length of 50 cm (0.8 mm internal diameter). Linear response for quinine concentrations (C) between 0.050 and 100.0 mg L-1 was described by: I = (532 ± 40) + (2.36 ± 0.04) C, with r = 0.999, where I is the relative fluorescence intensity. The coefficient of variation and limits of detection and quantification were 1.9% (0.50 mg L-1 n = 10), 2.3 and 4.5 mg L-1, respectively. The sampling throughput was 60 analyses per hour, consuming 2.2 mL of concentrated H2SO4 and producing 4 mL of wastes per analysis. No statistically significant differences were observed between the results obtained by the proposed SIA methodology and the ones obtained by the batch procedure. |
publishDate |
2011 |
dc.date.none.fl_str_mv |
2011-10-01 |
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=S0103-50532011001000009 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532011001000009 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0103-50532011001000009 |
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.22 n.10 2011 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_ |
1750318172689399808 |