Homogeneous electrocatalytic oxidation of d-penicillamine with ferrocyanide at a carbon paste electrode: application to voltammetric determination
The electrooxidation of d -penicillamine ( d -PA) was studied in the presence of ferrocyanide as a homogeneous mediator at the surface of a carbon paste electrode in aqueous media using cyclic voltammetry (CV) and chronoamperometry. Under optimum pH in CV the oxidation of d -PA occurs at a potential...
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Veröffentlicht in: | Journal of applied electrochemistry 2009-06, Vol.39 (6), p.799-805 |
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creator | Raoof, J. B. Ojani, R. Majidian, M. Chekin, F. |
description | The electrooxidation of
d
-penicillamine (
d
-PA) was studied in the presence of ferrocyanide as a homogeneous mediator at the surface of a carbon paste electrode in aqueous media using cyclic voltammetry (CV) and chronoamperometry. Under optimum pH in CV the oxidation of
d
-PA occurs at a potential about 380 mV less positive than that in the absence of ferrocyanide. The catalytic oxidation peak current was dependent on the
d
-PA concentration and a linear calibration curve was obtained in the ranges 4.0 × 10
−5
–2.0 × 10
−3
M and 8.0 × 10
−6
–1.8 × 10
−4
M of
d
-PA with CV and differential pulse voltammetry (DPV) methods, respectively. The detection limits (3σ) were determined as 1.9 × 10
−5
and 3.2 × 10
−6
M by CV and DPV methods. This method was also used for the determination of
d
-PA in pharmaceutical preparations by the standard addition method. |
doi_str_mv | 10.1007/s10800-008-9724-y |
format | Article |
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d
-penicillamine (
d
-PA) was studied in the presence of ferrocyanide as a homogeneous mediator at the surface of a carbon paste electrode in aqueous media using cyclic voltammetry (CV) and chronoamperometry. Under optimum pH in CV the oxidation of
d
-PA occurs at a potential about 380 mV less positive than that in the absence of ferrocyanide. The catalytic oxidation peak current was dependent on the
d
-PA concentration and a linear calibration curve was obtained in the ranges 4.0 × 10
−5
–2.0 × 10
−3
M and 8.0 × 10
−6
–1.8 × 10
−4
M of
d
-PA with CV and differential pulse voltammetry (DPV) methods, respectively. The detection limits (3σ) were determined as 1.9 × 10
−5
and 3.2 × 10
−6
M by CV and DPV methods. This method was also used for the determination of
d
-PA in pharmaceutical preparations by the standard addition method.</description><identifier>ISSN: 0021-891X</identifier><identifier>EISSN: 1572-8838</identifier><identifier>DOI: 10.1007/s10800-008-9724-y</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Anodizing ; Calibration ; Carbon ; Chemistry ; Chemistry and Materials Science ; Electrochemistry ; Electrodes ; Industrial Chemistry/Chemical Engineering ; Optimization ; Original Paper ; Oxidation ; Pastes ; Physical Chemistry ; Voltammetry</subject><ispartof>Journal of applied electrochemistry, 2009-06, Vol.39 (6), p.799-805</ispartof><rights>Springer Science+Business Media B.V. 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c321t-3f13e8e6ee813009ed4557e8f4c2083f1da3db56d738644077d25965840574eb3</citedby><cites>FETCH-LOGICAL-c321t-3f13e8e6ee813009ed4557e8f4c2083f1da3db56d738644077d25965840574eb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10800-008-9724-y$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10800-008-9724-y$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51297</link.rule.ids></links><search><creatorcontrib>Raoof, J. B.</creatorcontrib><creatorcontrib>Ojani, R.</creatorcontrib><creatorcontrib>Majidian, M.</creatorcontrib><creatorcontrib>Chekin, F.</creatorcontrib><title>Homogeneous electrocatalytic oxidation of d-penicillamine with ferrocyanide at a carbon paste electrode: application to voltammetric determination</title><title>Journal of applied electrochemistry</title><addtitle>J Appl Electrochem</addtitle><description>The electrooxidation of
d
-penicillamine (
d
-PA) was studied in the presence of ferrocyanide as a homogeneous mediator at the surface of a carbon paste electrode in aqueous media using cyclic voltammetry (CV) and chronoamperometry. Under optimum pH in CV the oxidation of
d
-PA occurs at a potential about 380 mV less positive than that in the absence of ferrocyanide. The catalytic oxidation peak current was dependent on the
d
-PA concentration and a linear calibration curve was obtained in the ranges 4.0 × 10
−5
–2.0 × 10
−3
M and 8.0 × 10
−6
–1.8 × 10
−4
M of
d
-PA with CV and differential pulse voltammetry (DPV) methods, respectively. The detection limits (3σ) were determined as 1.9 × 10
−5
and 3.2 × 10
−6
M by CV and DPV methods. This method was also used for the determination of
d
-PA in pharmaceutical preparations by the standard addition method.</description><subject>Anodizing</subject><subject>Calibration</subject><subject>Carbon</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Electrochemistry</subject><subject>Electrodes</subject><subject>Industrial Chemistry/Chemical Engineering</subject><subject>Optimization</subject><subject>Original Paper</subject><subject>Oxidation</subject><subject>Pastes</subject><subject>Physical Chemistry</subject><subject>Voltammetry</subject><issn>0021-891X</issn><issn>1572-8838</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNp9kMtu1TAURa0KJC6lH9CZh0wMx4_EDjNUQYtUiQlIzCxf-6R1lcTB9gXyG3wxbgNTRh6cvba1FyGXHN5wAP22cDAADMCwQQvFtjNy4J0WzBhpnpEDgODMDPzbC_KylAcAGESvDuT3TZrTHS6YToXihL7m5F1101ajp-lXDK7GtNA00sBWXKKP0-TmuCD9Ges9HTE3YHNLDEhdpY56l48NWF2p-K8x4Dvq1nWKfm-rif5IU3XzjDW3fwJWzK306fqKPB_dVPDi73tOvn788OXqht1-vv509f6WeSl4ZXLkEg32iIbLNgeD6jqNZlRegGnX4GQ4dn3Q0vRKgdZBdEPfGQWdVniU5-T13rvm9P2Epdo5Fo9t3pMNy3vNZT8ooVuU71GfUykZR7vmOLu8WQ720b_d_dvm3z76t1tjxM6Ull3uMNuHdMpLW_Qf6A8q14zW</recordid><startdate>20090601</startdate><enddate>20090601</enddate><creator>Raoof, J. B.</creator><creator>Ojani, R.</creator><creator>Majidian, M.</creator><creator>Chekin, F.</creator><general>Springer Netherlands</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20090601</creationdate><title>Homogeneous electrocatalytic oxidation of d-penicillamine with ferrocyanide at a carbon paste electrode: application to voltammetric determination</title><author>Raoof, J. B. ; Ojani, R. ; Majidian, M. ; Chekin, F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c321t-3f13e8e6ee813009ed4557e8f4c2083f1da3db56d738644077d25965840574eb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Anodizing</topic><topic>Calibration</topic><topic>Carbon</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Electrochemistry</topic><topic>Electrodes</topic><topic>Industrial Chemistry/Chemical Engineering</topic><topic>Optimization</topic><topic>Original Paper</topic><topic>Oxidation</topic><topic>Pastes</topic><topic>Physical Chemistry</topic><topic>Voltammetry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Raoof, J. B.</creatorcontrib><creatorcontrib>Ojani, R.</creatorcontrib><creatorcontrib>Majidian, M.</creatorcontrib><creatorcontrib>Chekin, F.</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Journal of applied electrochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Raoof, J. B.</au><au>Ojani, R.</au><au>Majidian, M.</au><au>Chekin, F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Homogeneous electrocatalytic oxidation of d-penicillamine with ferrocyanide at a carbon paste electrode: application to voltammetric determination</atitle><jtitle>Journal of applied electrochemistry</jtitle><stitle>J Appl Electrochem</stitle><date>2009-06-01</date><risdate>2009</risdate><volume>39</volume><issue>6</issue><spage>799</spage><epage>805</epage><pages>799-805</pages><issn>0021-891X</issn><eissn>1572-8838</eissn><abstract>The electrooxidation of
d
-penicillamine (
d
-PA) was studied in the presence of ferrocyanide as a homogeneous mediator at the surface of a carbon paste electrode in aqueous media using cyclic voltammetry (CV) and chronoamperometry. Under optimum pH in CV the oxidation of
d
-PA occurs at a potential about 380 mV less positive than that in the absence of ferrocyanide. The catalytic oxidation peak current was dependent on the
d
-PA concentration and a linear calibration curve was obtained in the ranges 4.0 × 10
−5
–2.0 × 10
−3
M and 8.0 × 10
−6
–1.8 × 10
−4
M of
d
-PA with CV and differential pulse voltammetry (DPV) methods, respectively. The detection limits (3σ) were determined as 1.9 × 10
−5
and 3.2 × 10
−6
M by CV and DPV methods. This method was also used for the determination of
d
-PA in pharmaceutical preparations by the standard addition method.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><doi>10.1007/s10800-008-9724-y</doi><tpages>7</tpages></addata></record> |
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subjects | Anodizing Calibration Carbon Chemistry Chemistry and Materials Science Electrochemistry Electrodes Industrial Chemistry/Chemical Engineering Optimization Original Paper Oxidation Pastes Physical Chemistry Voltammetry |
title | Homogeneous electrocatalytic oxidation of d-penicillamine with ferrocyanide at a carbon paste electrode: application to voltammetric determination |
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