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Simultaneous amperometric and potentiometric detection of inorganic anions in flow systems using platinum and silver/silver chloride electrodes
Platinum and silver/silver chloride electrodes were evaluated for electrochemical detection (amperometry and potentiometry, respectively) of inorganic anions in flow systems. In flow injection analysis, a linear response over three decades and detection limit of 1 × 10 −7 M for I − and NO 2 − were o...
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Published in: | Analytica chimica acta 1997-09, Vol.350 (1), p.1-6 |
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container_title | Analytica chimica acta |
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creator | Chen, Z. Hibbert, D.B. |
description | Platinum and silver/silver chloride electrodes were evaluated for electrochemical detection (amperometry and potentiometry, respectively) of inorganic anions in flow systems. In flow injection analysis, a linear response over three decades and detection limit of 1 × 10
−7 M for I
− and NO
2
− were obtained at an applied potential of +0.9 V (vs.
Ag
AgCl
) in 30 mM phosphate buffer at pH 3.0 as carrier. A silver/silver chloride electrode responded potentiometrically to halides and pseudo-halides in this buffer with a detection limit of 1 × 10
−5 M. The detector, which included both detection systems, was coupled with ion chromatography. Following separation by anion-exchange chromatography with 40 mM phosphate buffer at pH 4.5 as eluent, Cl
−, Br
−, I
−, SCN
−, and S
2O
3
2− were determined potentiometrically with a detection limit of 1 × 10
−5 M, and, simultaneously, NO
2
−,Br
−, I
−, and SCN
− were determined amperometrically with a detection limit of 1 × 10
−6 M. Ion-interaction chromatography with an eluent of 20 mM phosphate at pH 5.0 containing 5 mM tetrabutylammonium hydroxide separated and detected Br
−, NO
2
− and SCN
−. |
doi_str_mv | 10.1016/S0003-2670(97)00328-0 |
format | article |
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−7 M for I
− and NO
2
− were obtained at an applied potential of +0.9 V (vs.
Ag
AgCl
) in 30 mM phosphate buffer at pH 3.0 as carrier. A silver/silver chloride electrode responded potentiometrically to halides and pseudo-halides in this buffer with a detection limit of 1 × 10
−5 M. The detector, which included both detection systems, was coupled with ion chromatography. Following separation by anion-exchange chromatography with 40 mM phosphate buffer at pH 4.5 as eluent, Cl
−, Br
−, I
−, SCN
−, and S
2O
3
2− were determined potentiometrically with a detection limit of 1 × 10
−5 M, and, simultaneously, NO
2
−,Br
−, I
−, and SCN
− were determined amperometrically with a detection limit of 1 × 10
−6 M. Ion-interaction chromatography with an eluent of 20 mM phosphate at pH 5.0 containing 5 mM tetrabutylammonium hydroxide separated and detected Br
−, NO
2
− and SCN
−.</description><identifier>ISSN: 0003-2670</identifier><identifier>EISSN: 1873-4324</identifier><identifier>DOI: 10.1016/S0003-2670(97)00328-0</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>Electrochemical detection ; Flow injection ; Inorganic anions ; Ion chromatography</subject><ispartof>Analytica chimica acta, 1997-09, Vol.350 (1), p.1-6</ispartof><rights>1997</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c338t-7f4d2b152f077897f956d43c05f038abed92e6bf84773e9387c9499f5c69ae833</citedby><cites>FETCH-LOGICAL-c338t-7f4d2b152f077897f956d43c05f038abed92e6bf84773e9387c9499f5c69ae833</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27915,27916</link.rule.ids></links><search><creatorcontrib>Chen, Z.</creatorcontrib><creatorcontrib>Hibbert, D.B.</creatorcontrib><title>Simultaneous amperometric and potentiometric detection of inorganic anions in flow systems using platinum and silver/silver chloride electrodes</title><title>Analytica chimica acta</title><description>Platinum and silver/silver chloride electrodes were evaluated for electrochemical detection (amperometry and potentiometry, respectively) of inorganic anions in flow systems. In flow injection analysis, a linear response over three decades and detection limit of 1 × 10
−7 M for I
− and NO
2
− were obtained at an applied potential of +0.9 V (vs.
Ag
AgCl
) in 30 mM phosphate buffer at pH 3.0 as carrier. A silver/silver chloride electrode responded potentiometrically to halides and pseudo-halides in this buffer with a detection limit of 1 × 10
−5 M. The detector, which included both detection systems, was coupled with ion chromatography. Following separation by anion-exchange chromatography with 40 mM phosphate buffer at pH 4.5 as eluent, Cl
−, Br
−, I
−, SCN
−, and S
2O
3
2− were determined potentiometrically with a detection limit of 1 × 10
−5 M, and, simultaneously, NO
2
−,Br
−, I
−, and SCN
− were determined amperometrically with a detection limit of 1 × 10
−6 M. Ion-interaction chromatography with an eluent of 20 mM phosphate at pH 5.0 containing 5 mM tetrabutylammonium hydroxide separated and detected Br
−, NO
2
− and SCN
−.</description><subject>Electrochemical detection</subject><subject>Flow injection</subject><subject>Inorganic anions</subject><subject>Ion chromatography</subject><issn>0003-2670</issn><issn>1873-4324</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNqFkEFPHSEUhUmjSZ_P_oQmrJp2MZUZmGFYmcaoNTFxoa4JDy6WhoEpMDb-Cv-y-Ma67eree3LuSc6H0OeWfG9JO5zcEkJo0w2cfBX8W927sSEf0KYdOW0Y7dgB2rxbPqKjnH_Xs2sJ26DnWzctvqgAcclYTTOkOEFJTmMVDJ5jgVDcP8lAAV3PgKPFLsT0oMLeWaVcBWx9_IvzUy4wZbxkFx7w7FVxYZn2edn5R0gn68D6l4_JGcDga2yKBvIxOrTKZ_j0Nrfo_uL87uxnc31zeXX247rRlI6l4ZaZbtf2nSWcj4Jb0Q-GUU16S-iodmBEB8POjoxzCoKOXAsmhO31IBSMlG7RlzV3TvHPArnIyWUN3q8kZMcpo4z01divRp1izgmsnJObVHqSLZGv-OUev3xlKwWXe_yS1L_T9Q9qi0cHSWbtIGgwLtWy0kT3n4QXsvuQ1g</recordid><startdate>19970910</startdate><enddate>19970910</enddate><creator>Chen, Z.</creator><creator>Hibbert, D.B.</creator><general>Elsevier B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>19970910</creationdate><title>Simultaneous amperometric and potentiometric detection of inorganic anions in flow systems using platinum and silver/silver chloride electrodes</title><author>Chen, Z. ; Hibbert, D.B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c338t-7f4d2b152f077897f956d43c05f038abed92e6bf84773e9387c9499f5c69ae833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Electrochemical detection</topic><topic>Flow injection</topic><topic>Inorganic anions</topic><topic>Ion chromatography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Z.</creatorcontrib><creatorcontrib>Hibbert, D.B.</creatorcontrib><collection>CrossRef</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Analytica chimica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Z.</au><au>Hibbert, D.B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Simultaneous amperometric and potentiometric detection of inorganic anions in flow systems using platinum and silver/silver chloride electrodes</atitle><jtitle>Analytica chimica acta</jtitle><date>1997-09-10</date><risdate>1997</risdate><volume>350</volume><issue>1</issue><spage>1</spage><epage>6</epage><pages>1-6</pages><issn>0003-2670</issn><eissn>1873-4324</eissn><abstract>Platinum and silver/silver chloride electrodes were evaluated for electrochemical detection (amperometry and potentiometry, respectively) of inorganic anions in flow systems. In flow injection analysis, a linear response over three decades and detection limit of 1 × 10
−7 M for I
− and NO
2
− were obtained at an applied potential of +0.9 V (vs.
Ag
AgCl
) in 30 mM phosphate buffer at pH 3.0 as carrier. A silver/silver chloride electrode responded potentiometrically to halides and pseudo-halides in this buffer with a detection limit of 1 × 10
−5 M. The detector, which included both detection systems, was coupled with ion chromatography. Following separation by anion-exchange chromatography with 40 mM phosphate buffer at pH 4.5 as eluent, Cl
−, Br
−, I
−, SCN
−, and S
2O
3
2− were determined potentiometrically with a detection limit of 1 × 10
−5 M, and, simultaneously, NO
2
−,Br
−, I
−, and SCN
− were determined amperometrically with a detection limit of 1 × 10
−6 M. Ion-interaction chromatography with an eluent of 20 mM phosphate at pH 5.0 containing 5 mM tetrabutylammonium hydroxide separated and detected Br
−, NO
2
− and SCN
−.</abstract><pub>Elsevier B.V</pub><doi>10.1016/S0003-2670(97)00328-0</doi><tpages>6</tpages></addata></record> |
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ispartof | Analytica chimica acta, 1997-09, Vol.350 (1), p.1-6 |
issn | 0003-2670 1873-4324 |
language | eng |
recordid | cdi_proquest_miscellaneous_27343405 |
source | ScienceDirect Freedom Collection |
subjects | Electrochemical detection Flow injection Inorganic anions Ion chromatography |
title | Simultaneous amperometric and potentiometric detection of inorganic anions in flow systems using platinum and silver/silver chloride electrodes |
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