Simple Spectrophotometric Determination of Iron in Diesel Oil after Sample Preparation Employing Extraction Induced by Emulsion Breaking
Autor(a) principal: | |
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Data de Publicação: | 2022 |
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=S0103-50532022001001236 |
Resumo: | This work reports the development of a simple and fast method for the spectrophotometric determination of Fe in diesel oil using the classic reaction with 1,10-phenanthroline after its extraction induced by emulsion breaking (EIEB). The extraction parameters of EIEB were optimized (concentration of HNO3 and Triton X-100® in the emulsifying solution) as well as the adjustment of the pH of the final solution, a necessary step to complete the colorimetric reaction. The developed method presented a limit of detection of 0.004 mg L-1 and a limit of quantification of 0.013 mg L-1 and was applied in the analysis of six samples of diesel oil with different specifications. The results were statistically similar to those obtained by graphite furnace atomic absorption spectrometry (GF AAS). A recovery test was also performed by spiking the samples with 1.0 mg L-1 of Fe in the form of an organometallic compound, yielding recovery percentages between 83 and 108%. |
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Journal of the Brazilian Chemical Society (Online) |
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Simple Spectrophotometric Determination of Iron in Diesel Oil after Sample Preparation Employing Extraction Induced by Emulsion Breakingdiesel oilspectrophotometryironextraction induced by emulsion breakingThis work reports the development of a simple and fast method for the spectrophotometric determination of Fe in diesel oil using the classic reaction with 1,10-phenanthroline after its extraction induced by emulsion breaking (EIEB). The extraction parameters of EIEB were optimized (concentration of HNO3 and Triton X-100® in the emulsifying solution) as well as the adjustment of the pH of the final solution, a necessary step to complete the colorimetric reaction. The developed method presented a limit of detection of 0.004 mg L-1 and a limit of quantification of 0.013 mg L-1 and was applied in the analysis of six samples of diesel oil with different specifications. The results were statistically similar to those obtained by graphite furnace atomic absorption spectrometry (GF AAS). A recovery test was also performed by spiking the samples with 1.0 mg L-1 of Fe in the form of an organometallic compound, yielding recovery percentages between 83 and 108%.Sociedade Brasileira de Química2022-10-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532022001001236Journal of the Brazilian Chemical Society v.33 n.10 2022reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.21577/0103-5053.20220046info:eu-repo/semantics/openAccessPereira,Thamiris V.Cassella,Ricardo J.eng2022-10-07T00:00:00Zoai:scielo:S0103-50532022001001236Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2022-10-07T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Simple Spectrophotometric Determination of Iron in Diesel Oil after Sample Preparation Employing Extraction Induced by Emulsion Breaking |
title |
Simple Spectrophotometric Determination of Iron in Diesel Oil after Sample Preparation Employing Extraction Induced by Emulsion Breaking |
spellingShingle |
Simple Spectrophotometric Determination of Iron in Diesel Oil after Sample Preparation Employing Extraction Induced by Emulsion Breaking Pereira,Thamiris V. diesel oil spectrophotometry iron extraction induced by emulsion breaking |
title_short |
Simple Spectrophotometric Determination of Iron in Diesel Oil after Sample Preparation Employing Extraction Induced by Emulsion Breaking |
title_full |
Simple Spectrophotometric Determination of Iron in Diesel Oil after Sample Preparation Employing Extraction Induced by Emulsion Breaking |
title_fullStr |
Simple Spectrophotometric Determination of Iron in Diesel Oil after Sample Preparation Employing Extraction Induced by Emulsion Breaking |
title_full_unstemmed |
Simple Spectrophotometric Determination of Iron in Diesel Oil after Sample Preparation Employing Extraction Induced by Emulsion Breaking |
title_sort |
Simple Spectrophotometric Determination of Iron in Diesel Oil after Sample Preparation Employing Extraction Induced by Emulsion Breaking |
author |
Pereira,Thamiris V. |
author_facet |
Pereira,Thamiris V. Cassella,Ricardo J. |
author_role |
author |
author2 |
Cassella,Ricardo J. |
author2_role |
author |
dc.contributor.author.fl_str_mv |
Pereira,Thamiris V. Cassella,Ricardo J. |
dc.subject.por.fl_str_mv |
diesel oil spectrophotometry iron extraction induced by emulsion breaking |
topic |
diesel oil spectrophotometry iron extraction induced by emulsion breaking |
description |
This work reports the development of a simple and fast method for the spectrophotometric determination of Fe in diesel oil using the classic reaction with 1,10-phenanthroline after its extraction induced by emulsion breaking (EIEB). The extraction parameters of EIEB were optimized (concentration of HNO3 and Triton X-100® in the emulsifying solution) as well as the adjustment of the pH of the final solution, a necessary step to complete the colorimetric reaction. The developed method presented a limit of detection of 0.004 mg L-1 and a limit of quantification of 0.013 mg L-1 and was applied in the analysis of six samples of diesel oil with different specifications. The results were statistically similar to those obtained by graphite furnace atomic absorption spectrometry (GF AAS). A recovery test was also performed by spiking the samples with 1.0 mg L-1 of Fe in the form of an organometallic compound, yielding recovery percentages between 83 and 108%. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-10-01 |
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=S0103-50532022001001236 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532022001001236 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.21577/0103-5053.20220046 |
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.33 n.10 2022 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_ |
1750318185015410688 |