Indirect ultra trace determination of aminopolycarboxylic acids in surface water using ion exchange chromatography coupled on-line to inductively coupled plasma mass spectrometry.
Identifieur interne : 000C82 ( Main/Exploration ); précédent : 000C81; suivant : 000C83Indirect ultra trace determination of aminopolycarboxylic acids in surface water using ion exchange chromatography coupled on-line to inductively coupled plasma mass spectrometry.
Auteurs : RBID : pubmed:23218188English descriptors
- KwdEn :
- MESH :
- chemical , analysis : Edetic Acid, Nitrilotriacetic Acid, Water Pollutants, Chemical.
- chemical , chemistry : Indium, Iron.
- methods : Chromatography, Ion Exchange, Mass Spectrometry.
- Regression Analysis, Sensitivity and Specificity.
Abstract
An indirect method for the determination of ultra trace amounts of aminopolycarboxylic acids in surface water with a minimum of sample preparation was developed. It is based on the addition of a metal ion to the water sample in order to transform the chelating reagents into negatively charged complexes. These are separated by means of ion exchange chromatography and the metal inside the complex is detected by on-line coupled ICP-MS. Iron and indium as two metal ions of the nominal charge of +3 were investigated, whereas In(3+) provided the best results in terms of sensitivity with detection limits in the lower ng/l range. The trivalent complexing agent NTA cannot be determined accurately because of the low retention of the complex. The indium and iron complexes of CDTA are strongly absorbed on anion exchangers and showed retention time of over 1 h. The use of column-switching reduced the retention time to less than 15 min. The method has been validated against a sample set of 62 samples which have previously been analysed by an external water lab according to DIN EN ISO 16588 using the GC–MS method.
DOI: 10.1016/j.chroma.2012.11.015
PubMed: 23218188
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Le document en format XML
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<author><name sortKey="Kn Ll, J Rgen" uniqKey="Kn Ll J">Jürgen Knöll</name>
<affiliation wicri:level="3"><nlm:affiliation>University of Marburg, Chemistry Department, Analytical Chemistry, D-35032 Marburg, Germany.</nlm:affiliation>
<country xml:lang="fr">Allemagne</country>
<wicri:regionArea>University of Marburg, Chemistry Department, Analytical Chemistry, D-35032 Marburg</wicri:regionArea>
<placeName><region type="land" nuts="1">Hesse (Land)</region>
<region type="district" nuts="2">District de Giessen</region>
<settlement type="city">Marbourg</settlement>
</placeName>
</affiliation>
</author>
<author><name sortKey="Seubert, Andreas" uniqKey="Seubert A">Andreas Seubert</name>
</author>
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<publicationStmt><date when="2012">2012</date>
<idno type="doi">10.1016/j.chroma.2012.11.015</idno>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Chromatography, Ion Exchange (methods)</term>
<term>Edetic Acid (analysis)</term>
<term>Indium (chemistry)</term>
<term>Iron (chemistry)</term>
<term>Mass Spectrometry (methods)</term>
<term>Nitrilotriacetic Acid (analysis)</term>
<term>Regression Analysis</term>
<term>Sensitivity and Specificity</term>
<term>Water Pollutants, Chemical (analysis)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en"><term>Edetic Acid</term>
<term>Nitrilotriacetic Acid</term>
<term>Water Pollutants, Chemical</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>Indium</term>
<term>Iron</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Chromatography, Ion Exchange</term>
<term>Mass Spectrometry</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Regression Analysis</term>
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<front><div type="abstract" xml:lang="en">An indirect method for the determination of ultra trace amounts of aminopolycarboxylic acids in surface water with a minimum of sample preparation was developed. It is based on the addition of a metal ion to the water sample in order to transform the chelating reagents into negatively charged complexes. These are separated by means of ion exchange chromatography and the metal inside the complex is detected by on-line coupled ICP-MS. Iron and indium as two metal ions of the nominal charge of +3 were investigated, whereas In(3+) provided the best results in terms of sensitivity with detection limits in the lower ng/l range. The trivalent complexing agent NTA cannot be determined accurately because of the low retention of the complex. The indium and iron complexes of CDTA are strongly absorbed on anion exchangers and showed retention time of over 1 h. The use of column-switching reduced the retention time to less than 15 min. The method has been validated against a sample set of 62 samples which have previously been analysed by an external water lab according to DIN EN ISO 16588 using the GC–MS method.</div>
</front>
</TEI>
<pubmed><MedlineCitation Owner="NLM" Status="MEDLINE"><PMID Version="1">23218188</PMID>
<DateCreated><Year>2013</Year>
<Month>01</Month>
<Day>25</Day>
</DateCreated>
<DateCompleted><Year>2013</Year>
<Month>04</Month>
<Day>15</Day>
</DateCompleted>
<DateRevised><Year>2013</Year>
<Month>11</Month>
<Day>21</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Electronic">1873-3778</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>1270</Volume>
<PubDate><Year>2012</Year>
<Month>Dec</Month>
<Day>28</Day>
</PubDate>
</JournalIssue>
<Title>Journal of chromatography. A</Title>
<ISOAbbreviation>J Chromatogr A</ISOAbbreviation>
</Journal>
<ArticleTitle>Indirect ultra trace determination of aminopolycarboxylic acids in surface water using ion exchange chromatography coupled on-line to inductively coupled plasma mass spectrometry.</ArticleTitle>
<Pagination><MedlinePgn>219-24</MedlinePgn>
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<Abstract><AbstractText>An indirect method for the determination of ultra trace amounts of aminopolycarboxylic acids in surface water with a minimum of sample preparation was developed. It is based on the addition of a metal ion to the water sample in order to transform the chelating reagents into negatively charged complexes. These are separated by means of ion exchange chromatography and the metal inside the complex is detected by on-line coupled ICP-MS. Iron and indium as two metal ions of the nominal charge of +3 were investigated, whereas In(3+) provided the best results in terms of sensitivity with detection limits in the lower ng/l range. The trivalent complexing agent NTA cannot be determined accurately because of the low retention of the complex. The indium and iron complexes of CDTA are strongly absorbed on anion exchangers and showed retention time of over 1 h. The use of column-switching reduced the retention time to less than 15 min. The method has been validated against a sample set of 62 samples which have previously been analysed by an external water lab according to DIN EN ISO 16588 using the GC–MS method.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Knöll</LastName>
<ForeName>Jürgen</ForeName>
<Initials>J</Initials>
<Affiliation>University of Marburg, Chemistry Department, Analytical Chemistry, D-35032 Marburg, Germany.</Affiliation>
</Author>
<Author ValidYN="Y"><LastName>Seubert</LastName>
<ForeName>Andreas</ForeName>
<Initials>A</Initials>
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<Language>eng</Language>
<PublicationTypeList><PublicationType>Journal Article</PublicationType>
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<MedlineJournalInfo><Country>Netherlands</Country>
<MedlineTA>J Chromatogr A</MedlineTA>
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<NameOfSubstance>Indium</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>9G34HU7RV0</RegistryNumber>
<NameOfSubstance>Edetic Acid</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>E1UOL152H7</RegistryNumber>
<NameOfSubstance>Iron</NameOfSubstance>
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<Chemical><RegistryNumber>KA90006V9D</RegistryNumber>
<NameOfSubstance>Nitrilotriacetic Acid</NameOfSubstance>
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<MeshHeadingList><MeshHeading><DescriptorName MajorTopicYN="N">Chromatography, Ion Exchange</DescriptorName>
<QualifierName MajorTopicYN="Y">methods</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N">Edetic Acid</DescriptorName>
<QualifierName MajorTopicYN="Y">analysis</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N">Indium</DescriptorName>
<QualifierName MajorTopicYN="N">chemistry</QualifierName>
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<MeshHeading><DescriptorName MajorTopicYN="N">Iron</DescriptorName>
<QualifierName MajorTopicYN="N">chemistry</QualifierName>
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<MeshHeading><DescriptorName MajorTopicYN="N">Mass Spectrometry</DescriptorName>
<QualifierName MajorTopicYN="Y">methods</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N">Nitrilotriacetic Acid</DescriptorName>
<QualifierName MajorTopicYN="Y">analysis</QualifierName>
</MeshHeading>
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</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N">Sensitivity and Specificity</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N">Water Pollutants, Chemical</DescriptorName>
<QualifierName MajorTopicYN="Y">analysis</QualifierName>
</MeshHeading>
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<Day>13</Day>
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<PubMedPubDate PubStatus="revised"><Year>2012</Year>
<Month>11</Month>
<Day>7</Day>
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<PubMedPubDate PubStatus="accepted"><Year>2012</Year>
<Month>11</Month>
<Day>8</Day>
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