Serveur d'exploration sur le thulium

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

Synergic solvent extraction of lanthanides with mixtures of aliphatic fluorinated β-diketones and organophosphorus donors

Identifieur interne : 000923 ( Istex/Corpus ); précédent : 000922; suivant : 000924

Synergic solvent extraction of lanthanides with mixtures of aliphatic fluorinated β-diketones and organophosphorus donors

Auteurs : James W. Mitchel ; Charles V. Banks

Source :

RBID : ISTEX:29C3A0341A8F4BAD5DC149D0A7BC19DB1D893AC1

English descriptors

Abstract

Abstract: The extraction of lanthanides from an aqueous acetatechloride medium into cyclohexane solutions of trifluoroacetylacetone, hexafluoroacetylacctone, 6,6,7,7,8,8,8-heptafluoro-2,2-dimethyl-3,5-octanedione and tri-n-butyl phosphate was studied. The extraction properties of other fluorinated aliphatic β-diketones and fluoroorganophosphates were also investigated. The efficiency of the extraction of the lanthanides, the composition of the complexes transferred to the organic phase and the extraction and stability constants for the synergic reactions were determined. Synergic extraction, as a technique for the preparation of lanthanide species, was evaluated for compatibility with subsequent gas chromatography. The lanthanides were found to be rapidly and quantitatively transferred into organic phases containing mixtures of fluorinated aliphatic β-diketones and TBP. The resulting mixed complexes that contained fully fluorinated β-diketones had a distinct stoichiometry and were thermodynamically more stable dan similar mixed complexes of partially fluorinated β-diketones. These properties of the synergic systems allow precise control of the formation of anhydrous complexes in the organic phase and are compatible with the use of these systems for gas chromatography.

Url:
DOI: 10.1016/0039-9140(72)80056-0

Links to Exploration step

ISTEX:29C3A0341A8F4BAD5DC149D0A7BC19DB1D893AC1

Le document en format XML

<record>
<TEI wicri:istexFullTextTei="biblStruct">
<teiHeader>
<fileDesc>
<titleStmt>
<title>Synergic solvent extraction of lanthanides with mixtures of aliphatic fluorinated β-diketones and organophosphorus donors</title>
<author>
<name sortKey="Mitchel, James W" sort="Mitchel, James W" uniqKey="Mitchel J" first="James W." last="Mitchel">James W. Mitchel</name>
<affiliation>
<mods:affiliation>Institute for Atomic Research and Department of Chemistry, Iowa State University, Ames, Iowa 50010, U.S.A.</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Banks, Charles V" sort="Banks, Charles V" uniqKey="Banks C" first="Charles V." last="Banks">Charles V. Banks</name>
<affiliation>
<mods:affiliation>Institute for Atomic Research and Department of Chemistry, Iowa State University, Ames, Iowa 50010, U.S.A.</mods:affiliation>
</affiliation>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:29C3A0341A8F4BAD5DC149D0A7BC19DB1D893AC1</idno>
<date when="1972" year="1972">1972</date>
<idno type="doi">10.1016/0039-9140(72)80056-0</idno>
<idno type="url">https://api.istex.fr/document/29C3A0341A8F4BAD5DC149D0A7BC19DB1D893AC1/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">000923</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">000923</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title level="a">Synergic solvent extraction of lanthanides with mixtures of aliphatic fluorinated β-diketones and organophosphorus donors</title>
<author>
<name sortKey="Mitchel, James W" sort="Mitchel, James W" uniqKey="Mitchel J" first="James W." last="Mitchel">James W. Mitchel</name>
<affiliation>
<mods:affiliation>Institute for Atomic Research and Department of Chemistry, Iowa State University, Ames, Iowa 50010, U.S.A.</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Banks, Charles V" sort="Banks, Charles V" uniqKey="Banks C" first="Charles V." last="Banks">Charles V. Banks</name>
<affiliation>
<mods:affiliation>Institute for Atomic Research and Department of Chemistry, Iowa State University, Ames, Iowa 50010, U.S.A.</mods:affiliation>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series>
<title level="j">Talanta</title>
<title level="j" type="abbrev">TAL</title>
<idno type="ISSN">0039-9140</idno>
<imprint>
<publisher>ELSEVIER</publisher>
<date type="published" when="1972">1972</date>
<biblScope unit="volume">19</biblScope>
<biblScope unit="issue">10</biblScope>
<biblScope unit="page" from="1157">1157</biblScope>
<biblScope unit="page" to="1169">1169</biblScope>
</imprint>
<idno type="ISSN">0039-9140</idno>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt>
<idno type="ISSN">0039-9140</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Adduct</term>
<term>Aliphatiques fluor6es</term>
<term>Appropriate amounts</term>
<term>Aqueous phase</term>
<term>Aqueous phases</term>
<term>Atomic number</term>
<term>Cation</term>
<term>Chelate</term>
<term>Chem</term>
<term>Chloride ions</term>
<term>Cyclohexane</term>
<term>Distribution curves</term>
<term>Distribution ratio</term>
<term>Distriition ratio</term>
<term>Extraction</term>
<term>Extraction constants</term>
<term>Extraction curves</term>
<term>Extraction process</term>
<term>Hfod</term>
<term>Hfod ligand</term>
<term>Hhfa</term>
<term>Htfa</term>
<term>Ibid</term>
<term>Lanthanide</term>
<term>Ligand</term>
<term>Macro quantities</term>
<term>Mass action effect</term>
<term>Maximum number</term>
<term>Mole ratios</term>
<term>Neutral donor</term>
<term>Neutral donors</term>
<term>Organic phase</term>
<term>Organic phases</term>
<term>Overall reaction</term>
<term>Overall stability</term>
<term>Phase organique</term>
<term>Present study</term>
<term>Previous studies</term>
<term>Quantitative extraction</term>
<term>Rare earth</term>
<term>Rare earths</term>
<term>Reagent</term>
<term>Small amounts</term>
<term>Solvent extraction</term>
<term>Synergic</term>
<term>Synergic effect</term>
<term>Synergic extraction</term>
<term>Synergic system</term>
<term>Synergic systems</term>
<term>Tfep</term>
<term>Tracer quantities</term>
</keywords>
<keywords scheme="Teeft" xml:lang="en">
<term>Adduct</term>
<term>Aliphatiques fluor6es</term>
<term>Appropriate amounts</term>
<term>Aqueous phase</term>
<term>Aqueous phases</term>
<term>Atomic number</term>
<term>Cation</term>
<term>Chelate</term>
<term>Chem</term>
<term>Chloride ions</term>
<term>Cyclohexane</term>
<term>Distribution curves</term>
<term>Distribution ratio</term>
<term>Distriition ratio</term>
<term>Extraction</term>
<term>Extraction constants</term>
<term>Extraction curves</term>
<term>Extraction process</term>
<term>Hfod</term>
<term>Hfod ligand</term>
<term>Hhfa</term>
<term>Htfa</term>
<term>Ibid</term>
<term>Lanthanide</term>
<term>Ligand</term>
<term>Macro quantities</term>
<term>Mass action effect</term>
<term>Maximum number</term>
<term>Mole ratios</term>
<term>Neutral donor</term>
<term>Neutral donors</term>
<term>Organic phase</term>
<term>Organic phases</term>
<term>Overall reaction</term>
<term>Overall stability</term>
<term>Phase organique</term>
<term>Present study</term>
<term>Previous studies</term>
<term>Quantitative extraction</term>
<term>Rare earth</term>
<term>Rare earths</term>
<term>Reagent</term>
<term>Small amounts</term>
<term>Solvent extraction</term>
<term>Synergic</term>
<term>Synergic effect</term>
<term>Synergic extraction</term>
<term>Synergic system</term>
<term>Synergic systems</term>
<term>Tfep</term>
<term>Tracer quantities</term>
</keywords>
</textClass>
<langUsage>
<language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Abstract: The extraction of lanthanides from an aqueous acetatechloride medium into cyclohexane solutions of trifluoroacetylacetone, hexafluoroacetylacctone, 6,6,7,7,8,8,8-heptafluoro-2,2-dimethyl-3,5-octanedione and tri-n-butyl phosphate was studied. The extraction properties of other fluorinated aliphatic β-diketones and fluoroorganophosphates were also investigated. The efficiency of the extraction of the lanthanides, the composition of the complexes transferred to the organic phase and the extraction and stability constants for the synergic reactions were determined. Synergic extraction, as a technique for the preparation of lanthanide species, was evaluated for compatibility with subsequent gas chromatography. The lanthanides were found to be rapidly and quantitatively transferred into organic phases containing mixtures of fluorinated aliphatic β-diketones and TBP. The resulting mixed complexes that contained fully fluorinated β-diketones had a distinct stoichiometry and were thermodynamically more stable dan similar mixed complexes of partially fluorinated β-diketones. These properties of the synergic systems allow precise control of the formation of anhydrous complexes in the organic phase and are compatible with the use of these systems for gas chromatography.</div>
</front>
</TEI>
<istex>
<corpusName>elsevier</corpusName>
<keywords>
<teeft>
<json:string>lanthanide</json:string>
<json:string>synergic</json:string>
<json:string>hhfa</json:string>
<json:string>chelate</json:string>
<json:string>hfod</json:string>
<json:string>rare earths</json:string>
<json:string>cyclohexane</json:string>
<json:string>htfa</json:string>
<json:string>chem</json:string>
<json:string>cation</json:string>
<json:string>adduct</json:string>
<json:string>ibid</json:string>
<json:string>tfep</json:string>
<json:string>organic phase</json:string>
<json:string>extraction</json:string>
<json:string>aqueous phase</json:string>
<json:string>extraction constants</json:string>
<json:string>distribution ratio</json:string>
<json:string>reagent</json:string>
<json:string>synergic extraction</json:string>
<json:string>quantitative extraction</json:string>
<json:string>ligand</json:string>
<json:string>overall reaction</json:string>
<json:string>mass action effect</json:string>
<json:string>rare earth</json:string>
<json:string>synergic effect</json:string>
<json:string>organic phases</json:string>
<json:string>tracer quantities</json:string>
<json:string>extraction process</json:string>
<json:string>extraction curves</json:string>
<json:string>previous studies</json:string>
<json:string>synergic system</json:string>
<json:string>distriition ratio</json:string>
<json:string>macro quantities</json:string>
<json:string>neutral donor</json:string>
<json:string>solvent extraction</json:string>
<json:string>chloride ions</json:string>
<json:string>synergic systems</json:string>
<json:string>maximum number</json:string>
<json:string>appropriate amounts</json:string>
<json:string>hfod ligand</json:string>
<json:string>aqueous phases</json:string>
<json:string>distribution curves</json:string>
<json:string>mole ratios</json:string>
<json:string>atomic number</json:string>
<json:string>neutral donors</json:string>
<json:string>overall stability</json:string>
<json:string>aliphatiques fluor6es</json:string>
<json:string>phase organique</json:string>
<json:string>small amounts</json:string>
<json:string>present study</json:string>
</teeft>
</keywords>
<author>
<json:item>
<name>James W. Mitchel</name>
<affiliations>
<json:string>Institute for Atomic Research and Department of Chemistry, Iowa State University, Ames, Iowa 50010, U.S.A.</json:string>
</affiliations>
</json:item>
<json:item>
<name>Charles V. Banks</name>
<affiliations>
<json:string>Institute for Atomic Research and Department of Chemistry, Iowa State University, Ames, Iowa 50010, U.S.A.</json:string>
</affiliations>
</json:item>
</author>
<language>
<json:string>eng</json:string>
</language>
<originalGenre>
<json:string>Full-length article</json:string>
</originalGenre>
<abstract>The extraction of lanthanides from an aqueous acetatechloride medium into cyclohexane solutions of trifluoroacetylacetone, hexafluoroacetylacctone, 6,6,7,7,8,8,8-heptafluoro-2,2-dimethyl-3,5-octanedione and tri-n-butyl phosphate was studied. The extraction properties of other fluorinated aliphatic β-diketones and fluoroorganophosphates were also investigated. The efficiency of the extraction of the lanthanides, the composition of the complexes transferred to the organic phase and the extraction and stability constants for the synergic reactions were determined. Synergic extraction, as a technique for the preparation of lanthanide species, was evaluated for compatibility with subsequent gas chromatography. The lanthanides were found to be rapidly and quantitatively transferred into organic phases containing mixtures of fluorinated aliphatic β-diketones and TBP. The resulting mixed complexes that contained fully fluorinated β-diketones had a distinct stoichiometry and were thermodynamically more stable dan similar mixed complexes of partially fluorinated β-diketones. These properties of the synergic systems allow precise control of the formation of anhydrous complexes in the organic phase and are compatible with the use of these systems for gas chromatography.</abstract>
<qualityIndicators>
<score>6.688</score>
<pdfVersion>1.4</pdfVersion>
<pdfPageSize>468 x 684 pts</pdfPageSize>
<refBibsNative>true</refBibsNative>
<keywordCount>0</keywordCount>
<abstractCharCount>1278</abstractCharCount>
<pdfWordCount>4256</pdfWordCount>
<pdfCharCount>26810</pdfCharCount>
<pdfPageCount>13</pdfPageCount>
<abstractWordCount>161</abstractWordCount>
</qualityIndicators>
<title>Synergic solvent extraction of lanthanides with mixtures of aliphatic fluorinated β-diketones and organophosphorus donors</title>
<pii>
<json:string>0039-9140(72)80056-0</json:string>
</pii>
<genre>
<json:string>research-article</json:string>
</genre>
<serie>
<title>Advan. Chem. Series</title>
<language>
<json:string>unknown</json:string>
</language>
<volume>71</volume>
<pages>
<first>141</first>
<last>154</last>
</pages>
</serie>
<host>
<title>Talanta</title>
<language>
<json:string>unknown</json:string>
</language>
<publicationDate>1972</publicationDate>
<issn>
<json:string>0039-9140</json:string>
</issn>
<pii>
<json:string>S0039-9140(00)X0345-1</json:string>
</pii>
<volume>19</volume>
<issue>10</issue>
<pages>
<first>1157</first>
<last>1169</last>
</pages>
<genre>
<json:string>journal</json:string>
</genre>
</host>
<categories>
<wos>
<json:string>science</json:string>
<json:string>chemistry, analytical</json:string>
</wos>
<scienceMetrix>
<json:string>natural sciences</json:string>
<json:string>chemistry</json:string>
<json:string>analytical chemistry</json:string>
</scienceMetrix>
<inist>
<json:string>sciences appliquees, technologies et medecines</json:string>
<json:string>sciences biologiques et medicales</json:string>
<json:string>sciences biologiques fondamentales et appliquees. psychologie</json:string>
<json:string>biochimie analytique, structurale et metabolique</json:string>
</inist>
</categories>
<publicationDate>1972</publicationDate>
<copyrightDate>1972</copyrightDate>
<doi>
<json:string>10.1016/0039-9140(72)80056-0</json:string>
</doi>
<id>29C3A0341A8F4BAD5DC149D0A7BC19DB1D893AC1</id>
<score>1</score>
<fulltext>
<json:item>
<extension>pdf</extension>
<original>true</original>
<mimetype>application/pdf</mimetype>
<uri>https://api.istex.fr/document/29C3A0341A8F4BAD5DC149D0A7BC19DB1D893AC1/fulltext/pdf</uri>
</json:item>
<json:item>
<extension>zip</extension>
<original>false</original>
<mimetype>application/zip</mimetype>
<uri>https://api.istex.fr/document/29C3A0341A8F4BAD5DC149D0A7BC19DB1D893AC1/fulltext/zip</uri>
</json:item>
<istex:fulltextTEI uri="https://api.istex.fr/document/29C3A0341A8F4BAD5DC149D0A7BC19DB1D893AC1/fulltext/tei">
<teiHeader>
<fileDesc>
<titleStmt>
<title level="a">Synergic solvent extraction of lanthanides with mixtures of aliphatic fluorinated β-diketones and organophosphorus donors</title>
</titleStmt>
<publicationStmt>
<authority>ISTEX</authority>
<publisher>ELSEVIER</publisher>
<availability>
<p>ELSEVIER</p>
</availability>
<date>1972</date>
</publicationStmt>
<sourceDesc>
<biblStruct type="inbook">
<analytic>
<title level="a">Synergic solvent extraction of lanthanides with mixtures of aliphatic fluorinated β-diketones and organophosphorus donors</title>
<author xml:id="author-0000">
<persName>
<forename type="first">James W.</forename>
<surname>Mitchel</surname>
</persName>
<note type="biography">Present address: Bell Laboratories, Murray Hill, New Jersey 07974, U.S.A.</note>
<affiliation>Present address: Bell Laboratories, Murray Hill, New Jersey 07974, U.S.A.</affiliation>
<affiliation>Institute for Atomic Research and Department of Chemistry, Iowa State University, Ames, Iowa 50010, U.S.A.</affiliation>
</author>
<author xml:id="author-0001">
<persName>
<forename type="first">Charles V.</forename>
<surname>Banks</surname>
</persName>
<note type="biography">Deceased 29 February 1971.</note>
<affiliation>Deceased 29 February 1971.</affiliation>
<affiliation>Institute for Atomic Research and Department of Chemistry, Iowa State University, Ames, Iowa 50010, U.S.A.</affiliation>
</author>
<idno type="istex">29C3A0341A8F4BAD5DC149D0A7BC19DB1D893AC1</idno>
<idno type="DOI">10.1016/0039-9140(72)80056-0</idno>
<idno type="PII">0039-9140(72)80056-0</idno>
</analytic>
<monogr>
<title level="j">Talanta</title>
<title level="j" type="abbrev">TAL</title>
<idno type="pISSN">0039-9140</idno>
<idno type="PII">S0039-9140(00)X0345-1</idno>
<imprint>
<publisher>ELSEVIER</publisher>
<date type="published" when="1972"></date>
<biblScope unit="volume">19</biblScope>
<biblScope unit="issue">10</biblScope>
<biblScope unit="page" from="1157">1157</biblScope>
<biblScope unit="page" to="1169">1169</biblScope>
</imprint>
</monogr>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<creation>
<date>1972</date>
</creation>
<langUsage>
<language ident="en">en</language>
</langUsage>
<abstract xml:lang="en">
<p>The extraction of lanthanides from an aqueous acetatechloride medium into cyclohexane solutions of trifluoroacetylacetone, hexafluoroacetylacctone, 6,6,7,7,8,8,8-heptafluoro-2,2-dimethyl-3,5-octanedione and tri-n-butyl phosphate was studied. The extraction properties of other fluorinated aliphatic β-diketones and fluoroorganophosphates were also investigated. The efficiency of the extraction of the lanthanides, the composition of the complexes transferred to the organic phase and the extraction and stability constants for the synergic reactions were determined. Synergic extraction, as a technique for the preparation of lanthanide species, was evaluated for compatibility with subsequent gas chromatography. The lanthanides were found to be rapidly and quantitatively transferred into organic phases containing mixtures of fluorinated aliphatic β-diketones and TBP. The resulting mixed complexes that contained fully fluorinated β-diketones had a distinct stoichiometry and were thermodynamically more stable dan similar mixed complexes of partially fluorinated β-diketones. These properties of the synergic systems allow precise control of the formation of anhydrous complexes in the organic phase and are compatible with the use of these systems for gas chromatography.</p>
</abstract>
<abstract xml:lang="de">
<p>Zusammenfassung: Es wurde die Ausscheidung von Lanthaniden aus einem wässrigen Cloracetatmedium in Hexamethylenlösungen von Trifluoracctylaceton, Hexafluoracetylaceton, 6,6,7,7,8,8,8-Heptafluor2, 2-Äthan-3, 5-Oktanedion und Tri-n-Butylphosphat untersucht. Auch wurden die Ausscheidungseigenschaften anderer, fluorierter, aliphatischer β-Diketone und Fluororganophosphate untersucht. Es wurde die Wirksamkeit der Ausscheidung der Lanthaniden. die Zusammensetzung der Komplexverbindungen, welche in die organische Phase übergingen, und die Ausscheidung und Beständigkeitskonstanten für die synergetischen Reaktionen bestimmt. Es wurde die synergetische Ausscheidung ab ein Verfahren für die Vorbereitung von Lanthanidenarten im Hinblick auf Vereinbarkeit mit danachfolgender Gaschromatographie beurteilt. Es wurde gefunden, dass die Lanthaniden schnell und in Mengen in organische Phasen mit Mischungen von fluorierten aliphatischen β-Diketonen und TBP übergingen. Die resultierenden gemischten Komplexverbindungen enthielten voll fluorlerte β-Diketone, hatten eine deutliche Stöchiometrie und waren thermodynamisch beständiger als ähnliche Mischkomplexverbindungen von teilweise fluorierten β-Diktonen. Diese Eigenschaften der synergetischen Systeme ermöglichen genaue Kontrolle der Bildung anhydrischer Komplexverbindungen in der organischen Phase und sind mit Benutzung dieser Systeme mit Gas chromatographie vereinbar.</p>
</abstract>
<abstract xml:lang="fr">
<p>Résumé: On a étudié l'extraction de lanthanides d'un milieu aqueux acétate-chlorure dans des solutions en cyclohexanc de trifluoracétylacétone, hexafluoracétylacétone, 6,6,7,7,8,8,8-heptafluoro 2,2-diméthyl 3, 5-octanedione et tri-n-butyl phosphate. On a aussi examiné les propriétés d'extraction d'autres β-dicétones aliphatiques fluorées et fluoro-organophosphates. On a déterminé l'efficacité de l'extraction des lanthanides, la composition dea complexes transférés dans la phase organique et les constantes d'extraction et de stabilité pour les réactions synergiques. On a évalué l'extraction synergique, en tant que technique pour la préparation de l'espèce lanthanide, pour sa compatibilité avec une chromatographie en phase gazeuse subséquente. On a trouve que les lanthanides sont transférés rapidement et quantitativement dans des phases organiques contenant des mélanges de β-diacétooes aliphatiques fluorées et de TBP. Les complexes mixtes résultants contenant des β-dicétones totalement fluorées ont une stoechiométrie distincte et sont thermodynamiquement plus stables que les complexes mixtes similaires de β-dicétones partiellement fluorées. Ces propriétés des systèmes synergiques permettent un contrôle précis de la formation de complexes anhydres dans la phase organique et sont compatibles avec l'emploi de ces systèmes avec la chromatographie en phase gazeuse.</p>
</abstract>
</profileDesc>
<revisionDesc>
<change when="1972">Published</change>
</revisionDesc>
</teiHeader>
</istex:fulltextTEI>
<json:item>
<extension>txt</extension>
<original>false</original>
<mimetype>text/plain</mimetype>
<uri>https://api.istex.fr/document/29C3A0341A8F4BAD5DC149D0A7BC19DB1D893AC1/fulltext/txt</uri>
</json:item>
</fulltext>
<metadata>
<istex:metadataXml wicri:clean="Elsevier, elements deleted: tail">
<istex:xmlDeclaration>version="1.0" encoding="utf-8"</istex:xmlDeclaration>
<istex:docType PUBLIC="-//ES//DTD journal article DTD version 4.5.2//EN//XML" URI="art452.dtd" name="istex:docType"></istex:docType>
<istex:document>
<converted-article version="4.5.2" docsubtype="fla">
<item-info>
<jid>TAL</jid>
<aid>72800560</aid>
<ce:pii>0039-9140(72)80056-0</ce:pii>
<ce:doi>10.1016/0039-9140(72)80056-0</ce:doi>
<ce:copyright type="unknown" year="1972"></ce:copyright>
</item-info>
<head>
<ce:title>Synergic solvent extraction of lanthanides with mixtures of aliphatic fluorinated β-diketones and organophosphorus donors</ce:title>
<ce:author-group>
<ce:author>
<ce:given-name>James W.</ce:given-name>
<ce:surname>Mitchel</ce:surname>
<ce:cross-ref refid="FN1">
<ce:sup>1</ce:sup>
</ce:cross-ref>
</ce:author>
<ce:author>
<ce:given-name>Charles V.</ce:given-name>
<ce:surname>Banks</ce:surname>
<ce:cross-ref refid="FN2">
<ce:sup>2</ce:sup>
</ce:cross-ref>
</ce:author>
<ce:affiliation>
<ce:textfn>Institute for Atomic Research and Department of Chemistry, Iowa State University, Ames, Iowa 50010, U.S.A.</ce:textfn>
</ce:affiliation>
<ce:footnote id="FN1">
<ce:label>1</ce:label>
<ce:note-para>Present address: Bell Laboratories, Murray Hill, New Jersey 07974, U.S.A.</ce:note-para>
</ce:footnote>
<ce:footnote id="FN2">
<ce:label>2</ce:label>
<ce:note-para>Deceased 29 February 1971.</ce:note-para>
</ce:footnote>
</ce:author-group>
<ce:date-received day="24" month="8" year="1971"></ce:date-received>
<ce:date-accepted day="31" month="1" year="1972"></ce:date-accepted>
<ce:abstract>
<ce:section-title>Abstract</ce:section-title>
<ce:abstract-sec>
<ce:simple-para>The extraction of lanthanides from an aqueous acetatechloride medium into cyclohexane solutions of trifluoroacetylacetone, hexafluoroacetylacctone, 6,6,7,7,8,8,8-heptafluoro-2,2-dimethyl-3,5-octanedione and tri-n-butyl phosphate was studied. The extraction properties of other fluorinated aliphatic β-diketones and fluoroorganophosphates were also investigated. The efficiency of the extraction of the lanthanides, the composition of the complexes transferred to the organic phase and the extraction and stability constants for the synergic reactions were determined. Synergic extraction, as a technique for the preparation of lanthanide species, was evaluated for compatibility with subsequent gas chromatography. The lanthanides were found to be rapidly and quantitatively transferred into organic phases containing mixtures of fluorinated aliphatic β-diketones and TBP. The resulting mixed complexes that contained fully fluorinated β-diketones had a distinct stoichiometry and were thermodynamically more stable dan similar mixed complexes of partially fluorinated β-diketones. These properties of the synergic systems allow precise control of the formation of anhydrous complexes in the organic phase and are compatible with the use of these systems for gas chromatography.</ce:simple-para>
</ce:abstract-sec>
</ce:abstract>
<ce:abstract xml:lang="de">
<ce:section-title>Zusammenfassung</ce:section-title>
<ce:abstract-sec>
<ce:simple-para>Es wurde die Ausscheidung von Lanthaniden aus einem wässrigen Cloracetatmedium in Hexamethylenlösungen von Trifluoracctylaceton, Hexafluoracetylaceton, 6,6,7,7,8,8,8-Heptafluor2, 2-Äthan-3, 5-Oktanedion und Tri-
<ce:italic>n</ce:italic>
-Butylphosphat untersucht. Auch wurden die Ausscheidungseigenschaften anderer, fluorierter, aliphatischer β-Diketone und Fluororganophosphate untersucht. Es wurde die Wirksamkeit der Ausscheidung der Lanthaniden. die Zusammensetzung der Komplexverbindungen, welche in die organische Phase übergingen, und die Ausscheidung und Beständigkeitskonstanten für die synergetischen Reaktionen bestimmt. Es wurde die synergetische Ausscheidung ab ein Verfahren für die Vorbereitung von Lanthanidenarten im Hinblick auf Vereinbarkeit mit danachfolgender Gaschromatographie beurteilt. Es wurde gefunden, dass die Lanthaniden schnell und in Mengen in organische Phasen mit Mischungen von fluorierten aliphatischen β-Diketonen und TBP übergingen. Die resultierenden gemischten Komplexverbindungen enthielten voll fluorlerte β-Diketone, hatten eine deutliche Stöchiometrie und waren thermodynamisch beständiger als ähnliche Mischkomplexverbindungen von teilweise fluorierten β-Diktonen. Diese Eigenschaften der synergetischen Systeme ermöglichen genaue Kontrolle der Bildung anhydrischer Komplexverbindungen in der organischen Phase und sind mit Benutzung dieser Systeme mit Gas chromatographie vereinbar.</ce:simple-para>
</ce:abstract-sec>
</ce:abstract>
<ce:abstract xml:lang="fr">
<ce:section-title>Résumé</ce:section-title>
<ce:abstract-sec>
<ce:simple-para>On a étudié l'extraction de lanthanides d'un milieu aqueux acétate-chlorure dans des solutions en cyclohexanc de trifluoracétylacétone, hexafluoracétylacétone, 6,6,7,7,8,8,8-heptafluoro 2,2-diméthyl 3, 5-octanedione et tri-
<ce:italic>n</ce:italic>
-butyl phosphate. On a aussi examiné les propriétés d'extraction d'autres β-dicétones aliphatiques fluorées et fluoro-organophosphates. On a déterminé l'efficacité de l'extraction des lanthanides, la composition dea complexes transférés dans la phase organique et les constantes d'extraction et de stabilité pour les réactions synergiques. On a évalué l'extraction synergique, en tant que technique pour la préparation de l'espèce lanthanide, pour sa compatibilité avec une chromatographie en phase gazeuse subséquente. On a trouve que les lanthanides sont transférés rapidement et quantitativement dans des phases organiques contenant des mélanges de β-diacétooes aliphatiques fluorées et de TBP. Les complexes mixtes résultants contenant des β-dicétones totalement fluorées ont une stoechiométrie distincte et sont thermodynamiquement plus stables que les complexes mixtes similaires de β-dicétones partiellement fluorées. Ces propriétés des systèmes synergiques permettent un contrôle précis de la formation de complexes anhydres dans la phase organique et sont compatibles avec l'emploi de ces systèmes avec la chromatographie en phase gazeuse.</ce:simple-para>
</ce:abstract-sec>
</ce:abstract>
</head>
</converted-article>
</istex:document>
</istex:metadataXml>
<mods version="3.6">
<titleInfo>
<title>Synergic solvent extraction of lanthanides with mixtures of aliphatic fluorinated β-diketones and organophosphorus donors</title>
</titleInfo>
<titleInfo type="alternative" contentType="CDATA">
<title>Synergic solvent extraction of lanthanides with mixtures of aliphatic fluorinated β-diketones and organophosphorus donors</title>
</titleInfo>
<name type="personal">
<namePart type="given">James W.</namePart>
<namePart type="family">Mitchel</namePart>
<affiliation>Institute for Atomic Research and Department of Chemistry, Iowa State University, Ames, Iowa 50010, U.S.A.</affiliation>
<description>Present address: Bell Laboratories, Murray Hill, New Jersey 07974, U.S.A.</description>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Charles V.</namePart>
<namePart type="family">Banks</namePart>
<affiliation>Institute for Atomic Research and Department of Chemistry, Iowa State University, Ames, Iowa 50010, U.S.A.</affiliation>
<description>Deceased 29 February 1971.</description>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<typeOfResource>text</typeOfResource>
<genre type="research-article" displayLabel="Full-length article" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-1JC4F85T-7">research-article</genre>
<originInfo>
<publisher>ELSEVIER</publisher>
<dateIssued encoding="w3cdtf">1972</dateIssued>
<copyrightDate encoding="w3cdtf">1972</copyrightDate>
</originInfo>
<language>
<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
<languageTerm type="code" authority="rfc3066">en</languageTerm>
</language>
<abstract lang="en">Abstract: The extraction of lanthanides from an aqueous acetatechloride medium into cyclohexane solutions of trifluoroacetylacetone, hexafluoroacetylacctone, 6,6,7,7,8,8,8-heptafluoro-2,2-dimethyl-3,5-octanedione and tri-n-butyl phosphate was studied. The extraction properties of other fluorinated aliphatic β-diketones and fluoroorganophosphates were also investigated. The efficiency of the extraction of the lanthanides, the composition of the complexes transferred to the organic phase and the extraction and stability constants for the synergic reactions were determined. Synergic extraction, as a technique for the preparation of lanthanide species, was evaluated for compatibility with subsequent gas chromatography. The lanthanides were found to be rapidly and quantitatively transferred into organic phases containing mixtures of fluorinated aliphatic β-diketones and TBP. The resulting mixed complexes that contained fully fluorinated β-diketones had a distinct stoichiometry and were thermodynamically more stable dan similar mixed complexes of partially fluorinated β-diketones. These properties of the synergic systems allow precise control of the formation of anhydrous complexes in the organic phase and are compatible with the use of these systems for gas chromatography.</abstract>
<abstract lang="de">Zusammenfassung: Es wurde die Ausscheidung von Lanthaniden aus einem wässrigen Cloracetatmedium in Hexamethylenlösungen von Trifluoracctylaceton, Hexafluoracetylaceton, 6,6,7,7,8,8,8-Heptafluor2, 2-Äthan-3, 5-Oktanedion und Tri-n-Butylphosphat untersucht. Auch wurden die Ausscheidungseigenschaften anderer, fluorierter, aliphatischer β-Diketone und Fluororganophosphate untersucht. Es wurde die Wirksamkeit der Ausscheidung der Lanthaniden. die Zusammensetzung der Komplexverbindungen, welche in die organische Phase übergingen, und die Ausscheidung und Beständigkeitskonstanten für die synergetischen Reaktionen bestimmt. Es wurde die synergetische Ausscheidung ab ein Verfahren für die Vorbereitung von Lanthanidenarten im Hinblick auf Vereinbarkeit mit danachfolgender Gaschromatographie beurteilt. Es wurde gefunden, dass die Lanthaniden schnell und in Mengen in organische Phasen mit Mischungen von fluorierten aliphatischen β-Diketonen und TBP übergingen. Die resultierenden gemischten Komplexverbindungen enthielten voll fluorlerte β-Diketone, hatten eine deutliche Stöchiometrie und waren thermodynamisch beständiger als ähnliche Mischkomplexverbindungen von teilweise fluorierten β-Diktonen. Diese Eigenschaften der synergetischen Systeme ermöglichen genaue Kontrolle der Bildung anhydrischer Komplexverbindungen in der organischen Phase und sind mit Benutzung dieser Systeme mit Gas chromatographie vereinbar.</abstract>
<abstract lang="fr">Résumé: On a étudié l'extraction de lanthanides d'un milieu aqueux acétate-chlorure dans des solutions en cyclohexanc de trifluoracétylacétone, hexafluoracétylacétone, 6,6,7,7,8,8,8-heptafluoro 2,2-diméthyl 3, 5-octanedione et tri-n-butyl phosphate. On a aussi examiné les propriétés d'extraction d'autres β-dicétones aliphatiques fluorées et fluoro-organophosphates. On a déterminé l'efficacité de l'extraction des lanthanides, la composition dea complexes transférés dans la phase organique et les constantes d'extraction et de stabilité pour les réactions synergiques. On a évalué l'extraction synergique, en tant que technique pour la préparation de l'espèce lanthanide, pour sa compatibilité avec une chromatographie en phase gazeuse subséquente. On a trouve que les lanthanides sont transférés rapidement et quantitativement dans des phases organiques contenant des mélanges de β-diacétooes aliphatiques fluorées et de TBP. Les complexes mixtes résultants contenant des β-dicétones totalement fluorées ont une stoechiométrie distincte et sont thermodynamiquement plus stables que les complexes mixtes similaires de β-dicétones partiellement fluorées. Ces propriétés des systèmes synergiques permettent un contrôle précis de la formation de complexes anhydres dans la phase organique et sont compatibles avec l'emploi de ces systèmes avec la chromatographie en phase gazeuse.</abstract>
<relatedItem type="host">
<titleInfo>
<title>Talanta</title>
</titleInfo>
<titleInfo type="abbreviated">
<title>TAL</title>
</titleInfo>
<genre type="journal" authority="ISTEX" authorityURI="https://publication-type.data.istex.fr" valueURI="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</genre>
<originInfo>
<publisher>ELSEVIER</publisher>
<dateIssued encoding="w3cdtf">197210</dateIssued>
</originInfo>
<identifier type="ISSN">0039-9140</identifier>
<identifier type="PII">S0039-9140(00)X0345-1</identifier>
<part>
<date>197210</date>
<detail type="volume">
<number>19</number>
<caption>vol.</caption>
</detail>
<detail type="issue">
<number>10</number>
<caption>no.</caption>
</detail>
<extent unit="issue-pages">
<start>1085</start>
<end>1243</end>
</extent>
<extent unit="pages">
<start>1157</start>
<end>1169</end>
</extent>
</part>
</relatedItem>
<identifier type="istex">29C3A0341A8F4BAD5DC149D0A7BC19DB1D893AC1</identifier>
<identifier type="ark">ark:/67375/6H6-PHW9L035-S</identifier>
<identifier type="DOI">10.1016/0039-9140(72)80056-0</identifier>
<identifier type="PII">0039-9140(72)80056-0</identifier>
<recordInfo>
<recordContentSource authority="ISTEX" authorityURI="https://loaded-corpus.data.istex.fr" valueURI="https://loaded-corpus.data.istex.fr/ark:/67375/XBH-HKKZVM7B-M">elsevier</recordContentSource>
</recordInfo>
</mods>
<json:item>
<extension>json</extension>
<original>false</original>
<mimetype>application/json</mimetype>
<uri>https://api.istex.fr/document/29C3A0341A8F4BAD5DC149D0A7BC19DB1D893AC1/metadata/json</uri>
</json:item>
</metadata>
</istex>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Terre/explor/ThuliumV1/Data/Istex/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000923 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Istex/Corpus/biblio.hfd -nk 000923 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Terre
   |area=    ThuliumV1
   |flux=    Istex
   |étape=   Corpus
   |type=    RBID
   |clé=     ISTEX:29C3A0341A8F4BAD5DC149D0A7BC19DB1D893AC1
   |texte=   Synergic solvent extraction of lanthanides with mixtures of aliphatic fluorinated β-diketones and organophosphorus donors
}}

Wicri

This area was generated with Dilib version V0.6.21.
Data generation: Thu May 12 08:27:09 2016. Site generation: Thu Mar 7 22:33:44 2024