Redox and Complexatlon Interactions of Neptuniurn(V) with Quinonoid-Enriched Humic Derivatives

Actinides in their higher valence states (e.g., ... and ..., where M can be Np, Pu, etc) possess a higher potential for migration and in turn pose a substantial environmental threat. To minimize this potential for migration, reducing them to lower oxidation states (e.g., their tetravalent state) can...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Environmental science & technology 2007-10, Vol.41 (20), p.7010
Hauptverfasser: Shcherbina, Natalia S, Perminova, Irina V, Kalmykov, Stepan N, Kovalenko, Anton N, Haire, Richard G, Novikov, Alexander P
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue 20
container_start_page 7010
container_title Environmental science & technology
container_volume 41
creator Shcherbina, Natalia S
Perminova, Irina V
Kalmykov, Stepan N
Kovalenko, Anton N
Haire, Richard G
Novikov, Alexander P
description Actinides in their higher valence states (e.g., ... and ..., where M can be Np, Pu, etc) possess a higher potential for migration and in turn pose a substantial environmental threat. To minimize this potential for migration, reducing them to lower oxidation states (e.g., their tetravalent state) can be an attractive and efficient remedial process. These lower oxidation states are often much less soluble in natural aqueous media and are, therefore, less mobile in the environment. The research presented here focuses on assessing the performance of quinonoid-enriched humic derivatives with regards to complexing and/or reducing Np(V) present in solution. These "designer" humics are essentially derived reducing agents that can serve as reactive components of a novel humic-based remediation technology. The derivatives are obtained by incorporating different quinonoid-moieties into leonardite humic acids. Five quinonoid-derivatives are tested in this work and all five prove more effective as reducing agents for selected actinides than the parent leonardite humic acid, and the hydroquinone derivatives are better than the catechol derivatives. The reduction kinetics and the Np(V) species formed with the different derivatives are studied via a batch mode using near-infrared (NIR)-spectroscopy. Np(V) reduction by the humic derivatives under anoxic conditions at 293 K and at pH 4.7 obeys first-order kinetics. Rate constants range from 1.70 x 10... (parent humic acid) to 1.06 x 10... sec... (derivative with maximum hydroquinone content). Stability constants for Np(V)-humic complexes calculated from spectroscopic data produce corresponding Logβ values of 2.3 for parent humic acid and values ranging from 2.5 to 3.2 at pH 4.7 and from 3.3 to 3.7 at pH 7.4 for humic derivatives. Maximum constants are observed for hydroquinone-enriched derivatives. It is concluded that among the humic derivatives tested, the hydroquinone-enriched ones are the most useful for addressing remedial needs of actinide-contaminated aquifers. (ProQuest: ... denotes formulae/symbols omitted.)
format Article
fullrecord <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_journals_230139406</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1369764171</sourcerecordid><originalsourceid>FETCH-proquest_journals_2301394063</originalsourceid><addsrcrecordid>eNqNjrsKwkAQRbdQ8PkPg5UWgdUVMbUPtBEUEStlSUYcSWbiPtTPN4UfYHWLczjchmprPTZJambnlup4_9BaT4yet9XlgLl8wHIOCymrAj82FMKw5YDOZoGEPcgNdliFyBQdD08jeFO4wz4SCwvlyYodZXfMYRNLymCJjl420At9TzVvtvDY_21XDdar42KTVE6eEX24PqRu1uha_xmbdKpn5i_pC4YnQ2s</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>230139406</pqid></control><display><type>article</type><title>Redox and Complexatlon Interactions of Neptuniurn(V) with Quinonoid-Enriched Humic Derivatives</title><source>American Chemical Society Journals</source><creator>Shcherbina, Natalia S ; Perminova, Irina V ; Kalmykov, Stepan N ; Kovalenko, Anton N ; Haire, Richard G ; Novikov, Alexander P</creator><creatorcontrib>Shcherbina, Natalia S ; Perminova, Irina V ; Kalmykov, Stepan N ; Kovalenko, Anton N ; Haire, Richard G ; Novikov, Alexander P</creatorcontrib><description>Actinides in their higher valence states (e.g., ... and ..., where M can be Np, Pu, etc) possess a higher potential for migration and in turn pose a substantial environmental threat. To minimize this potential for migration, reducing them to lower oxidation states (e.g., their tetravalent state) can be an attractive and efficient remedial process. These lower oxidation states are often much less soluble in natural aqueous media and are, therefore, less mobile in the environment. The research presented here focuses on assessing the performance of quinonoid-enriched humic derivatives with regards to complexing and/or reducing Np(V) present in solution. These "designer" humics are essentially derived reducing agents that can serve as reactive components of a novel humic-based remediation technology. The derivatives are obtained by incorporating different quinonoid-moieties into leonardite humic acids. Five quinonoid-derivatives are tested in this work and all five prove more effective as reducing agents for selected actinides than the parent leonardite humic acid, and the hydroquinone derivatives are better than the catechol derivatives. The reduction kinetics and the Np(V) species formed with the different derivatives are studied via a batch mode using near-infrared (NIR)-spectroscopy. Np(V) reduction by the humic derivatives under anoxic conditions at 293 K and at pH 4.7 obeys first-order kinetics. Rate constants range from 1.70 x 10... (parent humic acid) to 1.06 x 10... sec... (derivative with maximum hydroquinone content). Stability constants for Np(V)-humic complexes calculated from spectroscopic data produce corresponding Logβ values of 2.3 for parent humic acid and values ranging from 2.5 to 3.2 at pH 4.7 and from 3.3 to 3.7 at pH 7.4 for humic derivatives. Maximum constants are observed for hydroquinone-enriched derivatives. It is concluded that among the humic derivatives tested, the hydroquinone-enriched ones are the most useful for addressing remedial needs of actinide-contaminated aquifers. (ProQuest: ... denotes formulae/symbols omitted.)</description><identifier>ISSN: 0013-936X</identifier><identifier>CODEN: ESTHAG</identifier><language>eng</language><publisher>Easton: American Chemical Society</publisher><subject>Chemical elements ; Chemical reactions ; Oxidation ; Reaction kinetics ; Spectrum analysis</subject><ispartof>Environmental science &amp; technology, 2007-10, Vol.41 (20), p.7010</ispartof><rights>Copyright American Chemical Society Oct 15, 2007</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids></links><search><creatorcontrib>Shcherbina, Natalia S</creatorcontrib><creatorcontrib>Perminova, Irina V</creatorcontrib><creatorcontrib>Kalmykov, Stepan N</creatorcontrib><creatorcontrib>Kovalenko, Anton N</creatorcontrib><creatorcontrib>Haire, Richard G</creatorcontrib><creatorcontrib>Novikov, Alexander P</creatorcontrib><title>Redox and Complexatlon Interactions of Neptuniurn(V) with Quinonoid-Enriched Humic Derivatives</title><title>Environmental science &amp; technology</title><description>Actinides in their higher valence states (e.g., ... and ..., where M can be Np, Pu, etc) possess a higher potential for migration and in turn pose a substantial environmental threat. To minimize this potential for migration, reducing them to lower oxidation states (e.g., their tetravalent state) can be an attractive and efficient remedial process. These lower oxidation states are often much less soluble in natural aqueous media and are, therefore, less mobile in the environment. The research presented here focuses on assessing the performance of quinonoid-enriched humic derivatives with regards to complexing and/or reducing Np(V) present in solution. These "designer" humics are essentially derived reducing agents that can serve as reactive components of a novel humic-based remediation technology. The derivatives are obtained by incorporating different quinonoid-moieties into leonardite humic acids. Five quinonoid-derivatives are tested in this work and all five prove more effective as reducing agents for selected actinides than the parent leonardite humic acid, and the hydroquinone derivatives are better than the catechol derivatives. The reduction kinetics and the Np(V) species formed with the different derivatives are studied via a batch mode using near-infrared (NIR)-spectroscopy. Np(V) reduction by the humic derivatives under anoxic conditions at 293 K and at pH 4.7 obeys first-order kinetics. Rate constants range from 1.70 x 10... (parent humic acid) to 1.06 x 10... sec... (derivative with maximum hydroquinone content). Stability constants for Np(V)-humic complexes calculated from spectroscopic data produce corresponding Logβ values of 2.3 for parent humic acid and values ranging from 2.5 to 3.2 at pH 4.7 and from 3.3 to 3.7 at pH 7.4 for humic derivatives. Maximum constants are observed for hydroquinone-enriched derivatives. It is concluded that among the humic derivatives tested, the hydroquinone-enriched ones are the most useful for addressing remedial needs of actinide-contaminated aquifers. (ProQuest: ... denotes formulae/symbols omitted.)</description><subject>Chemical elements</subject><subject>Chemical reactions</subject><subject>Oxidation</subject><subject>Reaction kinetics</subject><subject>Spectrum analysis</subject><issn>0013-936X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqNjrsKwkAQRbdQ8PkPg5UWgdUVMbUPtBEUEStlSUYcSWbiPtTPN4UfYHWLczjchmprPTZJambnlup4_9BaT4yet9XlgLl8wHIOCymrAj82FMKw5YDOZoGEPcgNdliFyBQdD08jeFO4wz4SCwvlyYodZXfMYRNLymCJjl420At9TzVvtvDY_21XDdar42KTVE6eEX24PqRu1uha_xmbdKpn5i_pC4YnQ2s</recordid><startdate>20071015</startdate><enddate>20071015</enddate><creator>Shcherbina, Natalia S</creator><creator>Perminova, Irina V</creator><creator>Kalmykov, Stepan N</creator><creator>Kovalenko, Anton N</creator><creator>Haire, Richard G</creator><creator>Novikov, Alexander P</creator><general>American Chemical Society</general><scope>7QO</scope><scope>7ST</scope><scope>7T7</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>SOI</scope></search><sort><creationdate>20071015</creationdate><title>Redox and Complexatlon Interactions of Neptuniurn(V) with Quinonoid-Enriched Humic Derivatives</title><author>Shcherbina, Natalia S ; Perminova, Irina V ; Kalmykov, Stepan N ; Kovalenko, Anton N ; Haire, Richard G ; Novikov, Alexander P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_2301394063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Chemical elements</topic><topic>Chemical reactions</topic><topic>Oxidation</topic><topic>Reaction kinetics</topic><topic>Spectrum analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shcherbina, Natalia S</creatorcontrib><creatorcontrib>Perminova, Irina V</creatorcontrib><creatorcontrib>Kalmykov, Stepan N</creatorcontrib><creatorcontrib>Kovalenko, Anton N</creatorcontrib><creatorcontrib>Haire, Richard G</creatorcontrib><creatorcontrib>Novikov, Alexander P</creatorcontrib><collection>Biotechnology Research Abstracts</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environment Abstracts</collection><jtitle>Environmental science &amp; technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shcherbina, Natalia S</au><au>Perminova, Irina V</au><au>Kalmykov, Stepan N</au><au>Kovalenko, Anton N</au><au>Haire, Richard G</au><au>Novikov, Alexander P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Redox and Complexatlon Interactions of Neptuniurn(V) with Quinonoid-Enriched Humic Derivatives</atitle><jtitle>Environmental science &amp; technology</jtitle><date>2007-10-15</date><risdate>2007</risdate><volume>41</volume><issue>20</issue><spage>7010</spage><pages>7010-</pages><issn>0013-936X</issn><coden>ESTHAG</coden><abstract>Actinides in their higher valence states (e.g., ... and ..., where M can be Np, Pu, etc) possess a higher potential for migration and in turn pose a substantial environmental threat. To minimize this potential for migration, reducing them to lower oxidation states (e.g., their tetravalent state) can be an attractive and efficient remedial process. These lower oxidation states are often much less soluble in natural aqueous media and are, therefore, less mobile in the environment. The research presented here focuses on assessing the performance of quinonoid-enriched humic derivatives with regards to complexing and/or reducing Np(V) present in solution. These "designer" humics are essentially derived reducing agents that can serve as reactive components of a novel humic-based remediation technology. The derivatives are obtained by incorporating different quinonoid-moieties into leonardite humic acids. Five quinonoid-derivatives are tested in this work and all five prove more effective as reducing agents for selected actinides than the parent leonardite humic acid, and the hydroquinone derivatives are better than the catechol derivatives. The reduction kinetics and the Np(V) species formed with the different derivatives are studied via a batch mode using near-infrared (NIR)-spectroscopy. Np(V) reduction by the humic derivatives under anoxic conditions at 293 K and at pH 4.7 obeys first-order kinetics. Rate constants range from 1.70 x 10... (parent humic acid) to 1.06 x 10... sec... (derivative with maximum hydroquinone content). Stability constants for Np(V)-humic complexes calculated from spectroscopic data produce corresponding Logβ values of 2.3 for parent humic acid and values ranging from 2.5 to 3.2 at pH 4.7 and from 3.3 to 3.7 at pH 7.4 for humic derivatives. Maximum constants are observed for hydroquinone-enriched derivatives. It is concluded that among the humic derivatives tested, the hydroquinone-enriched ones are the most useful for addressing remedial needs of actinide-contaminated aquifers. (ProQuest: ... denotes formulae/symbols omitted.)</abstract><cop>Easton</cop><pub>American Chemical Society</pub></addata></record>
fulltext fulltext
identifier ISSN: 0013-936X
ispartof Environmental science & technology, 2007-10, Vol.41 (20), p.7010
issn 0013-936X
language eng
recordid cdi_proquest_journals_230139406
source American Chemical Society Journals
subjects Chemical elements
Chemical reactions
Oxidation
Reaction kinetics
Spectrum analysis
title Redox and Complexatlon Interactions of Neptuniurn(V) with Quinonoid-Enriched Humic Derivatives
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T15%3A37%3A42IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Redox%20and%20Complexatlon%20Interactions%20of%20Neptuniurn(V)%20with%20Quinonoid-Enriched%20Humic%20Derivatives&rft.jtitle=Environmental%20science%20&%20technology&rft.au=Shcherbina,%20Natalia%20S&rft.date=2007-10-15&rft.volume=41&rft.issue=20&rft.spage=7010&rft.pages=7010-&rft.issn=0013-936X&rft.coden=ESTHAG&rft_id=info:doi/&rft_dat=%3Cproquest%3E1369764171%3C/proquest%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=230139406&rft_id=info:pmid/&rfr_iscdi=true