Application of capillary electrophoresis to anion speciation in soil water extracts: 2. Arsenic
A method has been developed for the speciation of arsenic (AsO{sub 2}{sup {minus}}, AsO{sub 4}{sup 3{minus}}, and dimethylarsinic [DMA]) in natural soil solutions from contaminated sites in Australia. The separation of these anions was achieved by capillary zone electrophoresis (CZE) using a fused s...
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creator | Naidu, R. Smith, J. McLaren, R.G. Stevens, D.P. Sumner, M.E. Jackson, P.E. |
description | A method has been developed for the speciation of arsenic (AsO{sub 2}{sup {minus}}, AsO{sub 4}{sup 3{minus}}, and dimethylarsinic [DMA]) in natural soil solutions from contaminated sites in Australia. The separation of these anions was achieved by capillary zone electrophoresis (CZE) using a fused silica capillary with a basic chromate buffer and on-column indirect UV detection at 254 nm. Method parameters, such as electrolyte pH, run voltage, and capillary temperature were studied in order to establish suitable analytical conditions. The ideal separation for As(III) and DMA was achieved with a buffer pH of 8.0, a run voltage of 25 kV, and a capillary temperature of 30 C. Under these conditions, As(V) and orthophosphate ions comigrated. However, the use of a chromate buffer at pH 10, a run voltage of 20 kV, and capillary temperature of 20 C led to complete separation of As(V) and phosphate peaks. Results of these investigations together with recovery test data suggest that separation of the As species from soil solutions can be achieved in less than 5 min with detection limits of 0.50, 0.10, and 0.10 mg L{sup {minus}1} for As(III), As(V), and DMA, respectively. |
doi_str_mv | 10.2136/sssaj2000.641122x |
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Arsenic</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Naidu, R. ; Smith, J. ; McLaren, R.G. ; Stevens, D.P. ; Sumner, M.E. ; Jackson, P.E.</creator><creatorcontrib>Naidu, R. ; Smith, J. ; McLaren, R.G. ; Stevens, D.P. ; Sumner, M.E. ; Jackson, P.E. ; CSIRO Land and Water and the Cooperative Research Centre for Soil and Land Management, Glen Osmond, South Australia (AU)</creatorcontrib><description>A method has been developed for the speciation of arsenic (AsO{sub 2}{sup {minus}}, AsO{sub 4}{sup 3{minus}}, and dimethylarsinic [DMA]) in natural soil solutions from contaminated sites in Australia. The separation of these anions was achieved by capillary zone electrophoresis (CZE) using a fused silica capillary with a basic chromate buffer and on-column indirect UV detection at 254 nm. Method parameters, such as electrolyte pH, run voltage, and capillary temperature were studied in order to establish suitable analytical conditions. The ideal separation for As(III) and DMA was achieved with a buffer pH of 8.0, a run voltage of 25 kV, and a capillary temperature of 30 C. Under these conditions, As(V) and orthophosphate ions comigrated. However, the use of a chromate buffer at pH 10, a run voltage of 20 kV, and capillary temperature of 20 C led to complete separation of As(V) and phosphate peaks. Results of these investigations together with recovery test data suggest that separation of the As species from soil solutions can be achieved in less than 5 min with detection limits of 0.50, 0.10, and 0.10 mg L{sup {minus}1} for As(III), As(V), and DMA, respectively.</description><identifier>ISSN: 0361-5995</identifier><identifier>EISSN: 1435-0661</identifier><identifier>DOI: 10.2136/sssaj2000.641122x</identifier><language>eng</language><publisher>United States</publisher><subject>ANIONS ; ARSENIC ; ELECTROPHORESIS ; ENVIRONMENTAL SCIENCES ; SOIL CHEMISTRY</subject><ispartof>Soil Science Society of America journal, 2000-02, Vol.64 (1)</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,777,781,882,27905,27906</link.rule.ids><backlink>$$Uhttps://www.osti.gov/biblio/20075800$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Naidu, R.</creatorcontrib><creatorcontrib>Smith, J.</creatorcontrib><creatorcontrib>McLaren, R.G.</creatorcontrib><creatorcontrib>Stevens, D.P.</creatorcontrib><creatorcontrib>Sumner, M.E.</creatorcontrib><creatorcontrib>Jackson, P.E.</creatorcontrib><creatorcontrib>CSIRO Land and Water and the Cooperative Research Centre for Soil and Land Management, Glen Osmond, South Australia (AU)</creatorcontrib><title>Application of capillary electrophoresis to anion speciation in soil water extracts: 2. Arsenic</title><title>Soil Science Society of America journal</title><description>A method has been developed for the speciation of arsenic (AsO{sub 2}{sup {minus}}, AsO{sub 4}{sup 3{minus}}, and dimethylarsinic [DMA]) in natural soil solutions from contaminated sites in Australia. The separation of these anions was achieved by capillary zone electrophoresis (CZE) using a fused silica capillary with a basic chromate buffer and on-column indirect UV detection at 254 nm. Method parameters, such as electrolyte pH, run voltage, and capillary temperature were studied in order to establish suitable analytical conditions. The ideal separation for As(III) and DMA was achieved with a buffer pH of 8.0, a run voltage of 25 kV, and a capillary temperature of 30 C. Under these conditions, As(V) and orthophosphate ions comigrated. However, the use of a chromate buffer at pH 10, a run voltage of 20 kV, and capillary temperature of 20 C led to complete separation of As(V) and phosphate peaks. Results of these investigations together with recovery test data suggest that separation of the As species from soil solutions can be achieved in less than 5 min with detection limits of 0.50, 0.10, and 0.10 mg L{sup {minus}1} for As(III), As(V), and DMA, respectively.</description><subject>ANIONS</subject><subject>ARSENIC</subject><subject>ELECTROPHORESIS</subject><subject>ENVIRONMENTAL SCIENCES</subject><subject>SOIL CHEMISTRY</subject><issn>0361-5995</issn><issn>1435-0661</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNqNjsFKAzEURUNR6Kj9gO4Crmd8yTSp466I4ge4H8Ljlb4SkpAXaP17R_QDXF0unMO9Sm0NDNaM_klEwtkCwOB3xlh7XanO7EbXg_fmRnUwetO7aXJrdSdyBjBuAujUfCglMobGOel81BgKxxjql6ZI2Goup1xJWHTLOqQfSgoh_wq8tMxRX0KjqunaasAmL9oO-lCFEuODuj2GKLT5y3v1-P72-frRZ2k8C3IjPGFOaRmbl_979www_o_6BvybTK4</recordid><startdate>20000201</startdate><enddate>20000201</enddate><creator>Naidu, R.</creator><creator>Smith, J.</creator><creator>McLaren, R.G.</creator><creator>Stevens, D.P.</creator><creator>Sumner, M.E.</creator><creator>Jackson, P.E.</creator><scope>OTOTI</scope></search><sort><creationdate>20000201</creationdate><title>Application of capillary electrophoresis to anion speciation in soil water extracts: 2. Arsenic</title><author>Naidu, R. ; Smith, J. ; McLaren, R.G. ; Stevens, D.P. ; Sumner, M.E. ; Jackson, P.E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-osti_scitechconnect_200758003</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>ANIONS</topic><topic>ARSENIC</topic><topic>ELECTROPHORESIS</topic><topic>ENVIRONMENTAL SCIENCES</topic><topic>SOIL CHEMISTRY</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Naidu, R.</creatorcontrib><creatorcontrib>Smith, J.</creatorcontrib><creatorcontrib>McLaren, R.G.</creatorcontrib><creatorcontrib>Stevens, D.P.</creatorcontrib><creatorcontrib>Sumner, M.E.</creatorcontrib><creatorcontrib>Jackson, P.E.</creatorcontrib><creatorcontrib>CSIRO Land and Water and the Cooperative Research Centre for Soil and Land Management, Glen Osmond, South Australia (AU)</creatorcontrib><collection>OSTI.GOV</collection><jtitle>Soil Science Society of America journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Naidu, R.</au><au>Smith, J.</au><au>McLaren, R.G.</au><au>Stevens, D.P.</au><au>Sumner, M.E.</au><au>Jackson, P.E.</au><aucorp>CSIRO Land and Water and the Cooperative Research Centre for Soil and Land Management, Glen Osmond, South Australia (AU)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Application of capillary electrophoresis to anion speciation in soil water extracts: 2. Arsenic</atitle><jtitle>Soil Science Society of America journal</jtitle><date>2000-02-01</date><risdate>2000</risdate><volume>64</volume><issue>1</issue><issn>0361-5995</issn><eissn>1435-0661</eissn><abstract>A method has been developed for the speciation of arsenic (AsO{sub 2}{sup {minus}}, AsO{sub 4}{sup 3{minus}}, and dimethylarsinic [DMA]) in natural soil solutions from contaminated sites in Australia. The separation of these anions was achieved by capillary zone electrophoresis (CZE) using a fused silica capillary with a basic chromate buffer and on-column indirect UV detection at 254 nm. Method parameters, such as electrolyte pH, run voltage, and capillary temperature were studied in order to establish suitable analytical conditions. The ideal separation for As(III) and DMA was achieved with a buffer pH of 8.0, a run voltage of 25 kV, and a capillary temperature of 30 C. Under these conditions, As(V) and orthophosphate ions comigrated. However, the use of a chromate buffer at pH 10, a run voltage of 20 kV, and capillary temperature of 20 C led to complete separation of As(V) and phosphate peaks. Results of these investigations together with recovery test data suggest that separation of the As species from soil solutions can be achieved in less than 5 min with detection limits of 0.50, 0.10, and 0.10 mg L{sup {minus}1} for As(III), As(V), and DMA, respectively.</abstract><cop>United States</cop><doi>10.2136/sssaj2000.641122x</doi></addata></record> |
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title | Application of capillary electrophoresis to anion speciation in soil water extracts: 2. Arsenic |
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