Determination of Selenium(IV) by Cathodic Stripping Voltammetry Using a Copper Microelectrode
Using a copper microelectrode of ∼5-μm diameter, the concentration of Se(IV) was determined by cathodic stripping voltammetry either from HClO4(0.1M) or from NaClO4(0.1M) supporting electrolytes. The preconcentration time of 15 s was chosen as optimal, and calibration graphs were constructed for the...
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Veröffentlicht in: | Microchemical journal 1997-10, Vol.57 (2), p.255-260 |
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creator | SUz̆, D. Blagojević, S. Vidić, J. Erceg, M. Vu c̆ć, D. |
description | Using a copper microelectrode of ∼5-μm diameter, the concentration of Se(IV) was determined by cathodic stripping voltammetry either from HClO4(0.1M) or from NaClO4(0.1M) supporting electrolytes. The preconcentration time of 15 s was chosen as optimal, and calibration graphs were constructed for the applied concentration interval 5 to 50 μM.Satisfactory reproducibility was obtained, with a standard deviation for 5 μMconcentration (n= 10) of about 4%. |
doi_str_mv | 10.1006/mchj.1997.1490 |
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The preconcentration time of 15 s was chosen as optimal, and calibration graphs were constructed for the applied concentration interval 5 to 50 μM.Satisfactory reproducibility was obtained, with a standard deviation for 5 μMconcentration (n= 10) of about 4%.</description><identifier>ISSN: 0026-265X</identifier><identifier>EISSN: 1095-9149</identifier><identifier>DOI: 10.1006/mchj.1997.1490</identifier><identifier>CODEN: MICJAN</identifier><language>eng</language><publisher>New York, NY: Elsevier B.V</publisher><subject>Analytical chemistry ; Chemistry ; Electrochemical methods ; Exact sciences and technology</subject><ispartof>Microchemical journal, 1997-10, Vol.57 (2), p.255-260</ispartof><rights>1997 Academic Press</rights><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c381t-d3d38f04b10732013347499e114c85fe28f5d45681e9ef9c9ef3b238944b09793</citedby><cites>FETCH-LOGICAL-c381t-d3d38f04b10732013347499e114c85fe28f5d45681e9ef9c9ef3b238944b09793</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0026265X97914909$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2058454$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>SUz̆, D.</creatorcontrib><creatorcontrib>Blagojević, S.</creatorcontrib><creatorcontrib>Vidić, J.</creatorcontrib><creatorcontrib>Erceg, M.</creatorcontrib><creatorcontrib>Vu c̆ć, D.</creatorcontrib><title>Determination of Selenium(IV) by Cathodic Stripping Voltammetry Using a Copper Microelectrode</title><title>Microchemical journal</title><description>Using a copper microelectrode of ∼5-μm diameter, the concentration of Se(IV) was determined by cathodic stripping voltammetry either from HClO4(0.1M) or from NaClO4(0.1M) supporting electrolytes. 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The preconcentration time of 15 s was chosen as optimal, and calibration graphs were constructed for the applied concentration interval 5 to 50 μM.Satisfactory reproducibility was obtained, with a standard deviation for 5 μMconcentration (n= 10) of about 4%.</abstract><cop>New York, NY</cop><pub>Elsevier B.V</pub><doi>10.1006/mchj.1997.1490</doi><tpages>6</tpages></addata></record> |
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title | Determination of Selenium(IV) by Cathodic Stripping Voltammetry Using a Copper Microelectrode |
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