Treatment of radioactive wastes: An X-ray absorption spectroscopy study of the reaction of technetium with green rust
Technetium is a long-lived product of nuclear fission that readily forms the soluble pertechnetate anion [TcO 4] −. Green rusts (layered hydrous oxides containing both Fe(II) and Fe(III) and with interlayer sulfate or carbonate anions) concentrate >99.8% of 99Tc, present as [TcO 4] −, from aqueou...
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Veröffentlicht in: | Journal of colloid and interface science 2003-12, Vol.268 (2), p.408-412 |
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container_title | Journal of colloid and interface science |
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creator | Pepper, Sarah E. Bunker, Debbie J. Bryan, Nicholas D. Livens, Francis R. Charnock, John M. Pattrick, Richard A.D. Collison, David |
description | Technetium is a long-lived product of nuclear fission that readily forms the soluble pertechnetate anion [TcO
4]
−. Green rusts (layered hydrous oxides containing both Fe(II) and Fe(III) and with interlayer sulfate or carbonate anions) concentrate >99.8% of
99Tc, present as [TcO
4]
−, from aqueous solution, even in the presence of high concentrations of NaNO
3, a common constituent of radioactive waste streams. The mechanism of removal from solution is apparently reduction and formation of strong Tc(IV) surface complexes. X-ray absorption spectroscopy shows that [TcO
4]
− is indeed reduced by reaction with both sulfate- and carbonate-form green rusts and is found in a TcO
2-like environment. On contact with air, the green rusts oxidize to poorly crystalline goethite but the Tc environment is unchanged. There is no increase in Tc solubility associated with oxidation of the host green rust. This behavior suggests that green rusts may be useful in the treatment of Tc-containing waste streams, in groundwater cleanup, and in restricting Tc migration from repositories. |
doi_str_mv | 10.1016/j.jcis.2003.08.024 |
format | Article |
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4]
−. Green rusts (layered hydrous oxides containing both Fe(II) and Fe(III) and with interlayer sulfate or carbonate anions) concentrate >99.8% of
99Tc, present as [TcO
4]
−, from aqueous solution, even in the presence of high concentrations of NaNO
3, a common constituent of radioactive waste streams. The mechanism of removal from solution is apparently reduction and formation of strong Tc(IV) surface complexes. X-ray absorption spectroscopy shows that [TcO
4]
− is indeed reduced by reaction with both sulfate- and carbonate-form green rusts and is found in a TcO
2-like environment. On contact with air, the green rusts oxidize to poorly crystalline goethite but the Tc environment is unchanged. There is no increase in Tc solubility associated with oxidation of the host green rust. This behavior suggests that green rusts may be useful in the treatment of Tc-containing waste streams, in groundwater cleanup, and in restricting Tc migration from repositories.</description><identifier>ISSN: 0021-9797</identifier><identifier>EISSN: 1095-7103</identifier><identifier>DOI: 10.1016/j.jcis.2003.08.024</identifier><identifier>PMID: 14643241</identifier><identifier>CODEN: JCISA5</identifier><language>eng</language><publisher>San Diego, CA: Elsevier Inc</publisher><subject>Chemistry ; Exact sciences and technology ; EXAFS spectroscopy ; General and physical chemistry ; Immobilization ; Radioactive waste ; Solid-liquid interface ; Surface complexation ; Surface physical chemistry ; Technetium</subject><ispartof>Journal of colloid and interface science, 2003-12, Vol.268 (2), p.408-412</ispartof><rights>2003 Elsevier Inc.</rights><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c382t-f489694f938171fe25aa5b3ae373cfa960ad26559cc9b5af472c33fe09cb7763</citedby><cites>FETCH-LOGICAL-c382t-f489694f938171fe25aa5b3ae373cfa960ad26559cc9b5af472c33fe09cb7763</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jcis.2003.08.024$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15328906$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14643241$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pepper, Sarah E.</creatorcontrib><creatorcontrib>Bunker, Debbie J.</creatorcontrib><creatorcontrib>Bryan, Nicholas D.</creatorcontrib><creatorcontrib>Livens, Francis R.</creatorcontrib><creatorcontrib>Charnock, John M.</creatorcontrib><creatorcontrib>Pattrick, Richard A.D.</creatorcontrib><creatorcontrib>Collison, David</creatorcontrib><title>Treatment of radioactive wastes: An X-ray absorption spectroscopy study of the reaction of technetium with green rust</title><title>Journal of colloid and interface science</title><addtitle>J Colloid Interface Sci</addtitle><description>Technetium is a long-lived product of nuclear fission that readily forms the soluble pertechnetate anion [TcO
4]
−. Green rusts (layered hydrous oxides containing both Fe(II) and Fe(III) and with interlayer sulfate or carbonate anions) concentrate >99.8% of
99Tc, present as [TcO
4]
−, from aqueous solution, even in the presence of high concentrations of NaNO
3, a common constituent of radioactive waste streams. The mechanism of removal from solution is apparently reduction and formation of strong Tc(IV) surface complexes. X-ray absorption spectroscopy shows that [TcO
4]
− is indeed reduced by reaction with both sulfate- and carbonate-form green rusts and is found in a TcO
2-like environment. On contact with air, the green rusts oxidize to poorly crystalline goethite but the Tc environment is unchanged. There is no increase in Tc solubility associated with oxidation of the host green rust. This behavior suggests that green rusts may be useful in the treatment of Tc-containing waste streams, in groundwater cleanup, and in restricting Tc migration from repositories.</description><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>EXAFS spectroscopy</subject><subject>General and physical chemistry</subject><subject>Immobilization</subject><subject>Radioactive waste</subject><subject>Solid-liquid interface</subject><subject>Surface complexation</subject><subject>Surface physical chemistry</subject><subject>Technetium</subject><issn>0021-9797</issn><issn>1095-7103</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNp9kE1v1DAQhq0K1G4Lf4AD8gVuCf5KHCMuVdUCUiUue-BmOc6Y9WoTB9tptf8ep7uCG6fRSM_7auZB6B0lNSW0_bSv99anmhHCa9LVhIkLtKFENZWkhL9CG0IYrZRU8gpdp7QnhNKmUZfoiopWcCboBi3bCCaPMGUcHI5m8MHY7J8AP5uUIX3GtxP-WUVzxKZPIc7ZhwmnGWyOIdkwH3HKy3Bc03kHuLTZF2Tdwe4myH4Z8bPPO_wrAkw4Lim_Qa-dOSR4e543aPtwv737Vj3--Pr97vaxsrxjuXKiU60STvGOSuqANcY0PTfAJbfOqJaYgbXlJWtV3xgnJLOcOyDK9lK2_AZ9PNXOMfxeIGU9-mThcDAThCVpSQUTvGsKyE6gLU-lCE7P0Y8mHjUlenWt93p1rVfXmnS6uC6h9-f2pR9h-Bc5yy3AhzNgkjUHF820dvzlGs46RdYzv5w4KCqePESdrIfJwuBj8ayH4P93xx_sQJ8U</recordid><startdate>20031215</startdate><enddate>20031215</enddate><creator>Pepper, Sarah E.</creator><creator>Bunker, Debbie J.</creator><creator>Bryan, Nicholas D.</creator><creator>Livens, Francis R.</creator><creator>Charnock, John M.</creator><creator>Pattrick, Richard A.D.</creator><creator>Collison, David</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20031215</creationdate><title>Treatment of radioactive wastes: An X-ray absorption spectroscopy study of the reaction of technetium with green rust</title><author>Pepper, Sarah E. ; Bunker, Debbie J. ; Bryan, Nicholas D. ; Livens, Francis R. ; Charnock, John M. ; Pattrick, Richard A.D. ; Collison, David</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c382t-f489694f938171fe25aa5b3ae373cfa960ad26559cc9b5af472c33fe09cb7763</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Chemistry</topic><topic>Exact sciences and technology</topic><topic>EXAFS spectroscopy</topic><topic>General and physical chemistry</topic><topic>Immobilization</topic><topic>Radioactive waste</topic><topic>Solid-liquid interface</topic><topic>Surface complexation</topic><topic>Surface physical chemistry</topic><topic>Technetium</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pepper, Sarah E.</creatorcontrib><creatorcontrib>Bunker, Debbie J.</creatorcontrib><creatorcontrib>Bryan, Nicholas D.</creatorcontrib><creatorcontrib>Livens, Francis R.</creatorcontrib><creatorcontrib>Charnock, John M.</creatorcontrib><creatorcontrib>Pattrick, Richard A.D.</creatorcontrib><creatorcontrib>Collison, David</creatorcontrib><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of colloid and interface science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pepper, Sarah E.</au><au>Bunker, Debbie J.</au><au>Bryan, Nicholas D.</au><au>Livens, Francis R.</au><au>Charnock, John M.</au><au>Pattrick, Richard A.D.</au><au>Collison, David</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Treatment of radioactive wastes: An X-ray absorption spectroscopy study of the reaction of technetium with green rust</atitle><jtitle>Journal of colloid and interface science</jtitle><addtitle>J Colloid Interface Sci</addtitle><date>2003-12-15</date><risdate>2003</risdate><volume>268</volume><issue>2</issue><spage>408</spage><epage>412</epage><pages>408-412</pages><issn>0021-9797</issn><eissn>1095-7103</eissn><coden>JCISA5</coden><abstract>Technetium is a long-lived product of nuclear fission that readily forms the soluble pertechnetate anion [TcO
4]
−. Green rusts (layered hydrous oxides containing both Fe(II) and Fe(III) and with interlayer sulfate or carbonate anions) concentrate >99.8% of
99Tc, present as [TcO
4]
−, from aqueous solution, even in the presence of high concentrations of NaNO
3, a common constituent of radioactive waste streams. The mechanism of removal from solution is apparently reduction and formation of strong Tc(IV) surface complexes. X-ray absorption spectroscopy shows that [TcO
4]
− is indeed reduced by reaction with both sulfate- and carbonate-form green rusts and is found in a TcO
2-like environment. On contact with air, the green rusts oxidize to poorly crystalline goethite but the Tc environment is unchanged. There is no increase in Tc solubility associated with oxidation of the host green rust. This behavior suggests that green rusts may be useful in the treatment of Tc-containing waste streams, in groundwater cleanup, and in restricting Tc migration from repositories.</abstract><cop>San Diego, CA</cop><pub>Elsevier Inc</pub><pmid>14643241</pmid><doi>10.1016/j.jcis.2003.08.024</doi><tpages>5</tpages></addata></record> |
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source | Elsevier ScienceDirect Journals Complete - AutoHoldings |
subjects | Chemistry Exact sciences and technology EXAFS spectroscopy General and physical chemistry Immobilization Radioactive waste Solid-liquid interface Surface complexation Surface physical chemistry Technetium |
title | Treatment of radioactive wastes: An X-ray absorption spectroscopy study of the reaction of technetium with green rust |
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