Voltammetric determination of Ioxynil and 2-methyl-3-nitroaniline using C(18) modified carbon paste electrodes.
Identifieur interne : 000953 ( PubMed/Corpus ); précédent : 000952; suivant : 000954Voltammetric determination of Ioxynil and 2-methyl-3-nitroaniline using C(18) modified carbon paste electrodes.
Auteurs : C. Faller ; A. Meyer ; G. HenzeSource :
- Analytical and bioanalytical chemistry [ 1618-2650 ] ; 1996.
Abstract
The stripping voltammetric behaviour of Ioxynil and 2-methyl-3-nitroaniline has been studied by means of a C(18) modified carbon paste electrode. The analytes are preconcentrated under open-circuit conditions (Ioxynil at pH 3.9; 2-methyl-3-nitroaniline at pH 10). For the determination of Ioxynil and 2-methyl-3-nitroaniline 0.01 mol/l HCl and 1 mol/l KOH, respectively, have been used as supporting electrolyte. Under optimized conditions detection limits up to 0.1 microg/ml Ioxynil and 0.3 microg/ml 2-methyl-3-nitroaniline have been obtained. The methods have been applied to the determination of Ioxynil and 2-methyl-3-nitroaniline in drinking water.
DOI: 10.1007/s0021663560279
PubMed: 15048369
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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Voltammetric determination of Ioxynil and 2-methyl-3-nitroaniline using C(18) modified carbon paste electrodes.</title><author><name sortKey="Faller, C" sort="Faller, C" uniqKey="Faller C" first="C" last="Faller">C. Faller</name><affiliation><nlm:affiliation>Fachbereich Chemie der Universität Kaiserslautern und Abteilung für Anorganische und Analytische Chemie der Universität Trier, Postfach 3825, D-54228, Trier, Germany.</nlm:affiliation></affiliation></author><author><name sortKey="Meyer, A" sort="Meyer, A" uniqKey="Meyer A" first="A" last="Meyer">A. Meyer</name></author><author><name sortKey="Henze, G" sort="Henze, G" uniqKey="Henze G" first="G" last="Henze">G. Henze</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="1996">1996</date><idno type="RBID">pubmed:15048369</idno><idno type="pmid">15048369</idno><idno type="doi">10.1007/s0021663560279</idno><idno type="wicri:Area/PubMed/Corpus">000953</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">000953</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Voltammetric determination of Ioxynil and 2-methyl-3-nitroaniline using C(18) modified carbon paste electrodes.</title><author><name sortKey="Faller, C" sort="Faller, C" uniqKey="Faller C" first="C" last="Faller">C. Faller</name><affiliation><nlm:affiliation>Fachbereich Chemie der Universität Kaiserslautern und Abteilung für Anorganische und Analytische Chemie der Universität Trier, Postfach 3825, D-54228, Trier, Germany.</nlm:affiliation></affiliation></author><author><name sortKey="Meyer, A" sort="Meyer, A" uniqKey="Meyer A" first="A" last="Meyer">A. Meyer</name></author><author><name sortKey="Henze, G" sort="Henze, G" uniqKey="Henze G" first="G" last="Henze">G. Henze</name></author></analytic><series><title level="j">Analytical and bioanalytical chemistry</title><idno type="eISSN">1618-2650</idno><imprint><date when="1996" type="published">1996</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The stripping voltammetric behaviour of Ioxynil and 2-methyl-3-nitroaniline has been studied by means of a C(18) modified carbon paste electrode. The analytes are preconcentrated under open-circuit conditions (Ioxynil at pH 3.9; 2-methyl-3-nitroaniline at pH 10). For the determination of Ioxynil and 2-methyl-3-nitroaniline 0.01 mol/l HCl and 1 mol/l KOH, respectively, have been used as supporting electrolyte. Under optimized conditions detection limits up to 0.1 microg/ml Ioxynil and 0.3 microg/ml 2-methyl-3-nitroaniline have been obtained. The methods have been applied to the determination of Ioxynil and 2-methyl-3-nitroaniline in drinking water.</div></front></TEI><pubmed><MedlineCitation Status="Publisher" Owner="NLM"><PMID Version="1">15048369</PMID><DateCreated><Year>2004</Year><Month>03</Month><Day>29</Day></DateCreated><DateRevised><Year>2004</Year><Month>03</Month><Day>29</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Electronic">1618-2650</ISSN><JournalIssue CitedMedium="Internet"><Volume>356</Volume><Issue>3-4</Issue><PubDate><Year>1996</Year><Month>Sep</Month></PubDate></JournalIssue><Title>Analytical and bioanalytical chemistry</Title><ISOAbbreviation>Anal Bioanal Chem</ISOAbbreviation></Journal><ArticleTitle>Voltammetric determination of Ioxynil and 2-methyl-3-nitroaniline using C(18) modified carbon paste electrodes.</ArticleTitle><Pagination><MedlinePgn>279-83</MedlinePgn></Pagination><Abstract><AbstractText>The stripping voltammetric behaviour of Ioxynil and 2-methyl-3-nitroaniline has been studied by means of a C(18) modified carbon paste electrode. The analytes are preconcentrated under open-circuit conditions (Ioxynil at pH 3.9; 2-methyl-3-nitroaniline at pH 10). For the determination of Ioxynil and 2-methyl-3-nitroaniline 0.01 mol/l HCl and 1 mol/l KOH, respectively, have been used as supporting electrolyte. Under optimized conditions detection limits up to 0.1 microg/ml Ioxynil and 0.3 microg/ml 2-methyl-3-nitroaniline have been obtained. The methods have been applied to the determination of Ioxynil and 2-methyl-3-nitroaniline in drinking water.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Faller</LastName><ForeName>C</ForeName><Initials>C</Initials><AffiliationInfo><Affiliation>Fachbereich Chemie der Universität Kaiserslautern und Abteilung für Anorganische und Analytische Chemie der Universität Trier, Postfach 3825, D-54228, Trier, Germany.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Meyer</LastName><ForeName>A</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Henze</LastName><ForeName>G</ForeName><Initials>G</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="">Journal Article</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>Germany</Country><MedlineTA>Anal Bioanal Chem</MedlineTA><NlmUniqueID>101134327</NlmUniqueID><ISSNLinking>1618-2642</ISSNLinking></MedlineJournalInfo></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>1995</Year><Month>12</Month><Day>14</Day></PubMedPubDate><PubMedPubDate PubStatus="revised"><Year>1996</Year><Month>03</Month><Day>27</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>1996</Year><Month>04</Month><Day>04</Day></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>1996</Year><Month>9</Month><Day>1</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>1996</Year><Month>9</Month><Day>1</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>1996</Year><Month>9</Month><Day>1</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">15048369</ArticleId><ArticleId IdType="doi">10.1007/s0021663560279</ArticleId></ArticleIdList></PubmedData></pubmed></record>Pour manipuler ce document sous Unix (Dilib)
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