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Voltammetric Investigation of the Oxidation of Iron Powder
Voltammetry measurements were performed on iron powder particles of various size fractions immobilized on the surface of a paraffin-impregnated graphite electrode in electrolytes of various pH values. The course of voltammetric curves implies that the start of the dissolution process is shifted nega...
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Published in: | Particulate science and technology 2005-04, Vol.23 (2), p.189-199 |
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cites | cdi_FETCH-LOGICAL-c407t-82b6c6a324ee07cc7f9e4ef7c43d7f64ca3f53d70c13915fa6edf2a0e017d34f3 |
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container_title | Particulate science and technology |
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creator | Kladeková, Daniela Gálová, Miriam Pikna, L'ubomír |
description | Voltammetry measurements were performed on iron powder particles of various size fractions immobilized on the surface of a paraffin-impregnated graphite electrode in electrolytes of various pH values. The course of voltammetric curves implies that the start of the dissolution process is shifted negatively with increasing pH value and the anodic dissolution process of iron is inhibited due to adsorption of products of the electrode reaction on iron particle surfaces. The rate of dissolution is changed also with iron particle size: decreasing dissolution rate and appearance of inhibition were encountered with an increase in particle size. A mechanism was suggested taking into account the influence of both pH of the electrolyte and particle size fraction. Electrochemical dissolution of freshly reduced iron from the solution proceeds at a lower potential than the same process of iron powder immobilized on the electrode. |
doi_str_mv | 10.1080/02726350590922260 |
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The course of voltammetric curves implies that the start of the dissolution process is shifted negatively with increasing pH value and the anodic dissolution process of iron is inhibited due to adsorption of products of the electrode reaction on iron particle surfaces. The rate of dissolution is changed also with iron particle size: decreasing dissolution rate and appearance of inhibition were encountered with an increase in particle size. A mechanism was suggested taking into account the influence of both pH of the electrolyte and particle size fraction. Electrochemical dissolution of freshly reduced iron from the solution proceeds at a lower potential than the same process of iron powder immobilized on the electrode.</description><identifier>ISSN: 0272-6351</identifier><identifier>EISSN: 1548-0046</identifier><identifier>DOI: 10.1080/02726350590922260</identifier><identifier>CODEN: PTCHDS</identifier><language>eng</language><publisher>Washington, DC: Taylor & Francis Group</publisher><subject>Chemistry ; Colloidal state and disperse state ; electrochemical dissolution ; Exact sciences and technology ; General and physical chemistry ; iron ; powder particles ; Surface physical chemistry ; voltammetry</subject><ispartof>Particulate science and technology, 2005-04, Vol.23 (2), p.189-199</ispartof><rights>Copyright Taylor & Francis Group, LLC 2005</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c407t-82b6c6a324ee07cc7f9e4ef7c43d7f64ca3f53d70c13915fa6edf2a0e017d34f3</citedby><cites>FETCH-LOGICAL-c407t-82b6c6a324ee07cc7f9e4ef7c43d7f64ca3f53d70c13915fa6edf2a0e017d34f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16862457$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Kladeková, Daniela</creatorcontrib><creatorcontrib>Gálová, Miriam</creatorcontrib><creatorcontrib>Pikna, L'ubomír</creatorcontrib><title>Voltammetric Investigation of the Oxidation of Iron Powder</title><title>Particulate science and technology</title><description>Voltammetry measurements were performed on iron powder particles of various size fractions immobilized on the surface of a paraffin-impregnated graphite electrode in electrolytes of various pH values. The course of voltammetric curves implies that the start of the dissolution process is shifted negatively with increasing pH value and the anodic dissolution process of iron is inhibited due to adsorption of products of the electrode reaction on iron particle surfaces. The rate of dissolution is changed also with iron particle size: decreasing dissolution rate and appearance of inhibition were encountered with an increase in particle size. A mechanism was suggested taking into account the influence of both pH of the electrolyte and particle size fraction. Electrochemical dissolution of freshly reduced iron from the solution proceeds at a lower potential than the same process of iron powder immobilized on the electrode.</description><subject>Chemistry</subject><subject>Colloidal state and disperse state</subject><subject>electrochemical dissolution</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>iron</subject><subject>powder particles</subject><subject>Surface physical chemistry</subject><subject>voltammetry</subject><issn>0272-6351</issn><issn>1548-0046</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqFkEtPwzAMgCMEEmPwA7j1AreC824RFzTxmDRpHIBrFdIEgtpmJBnb_j2dNuCABCdb9vfZlhE6xnCGoYBzIJIIyoGXUBJCBOygAeasyAGY2EWDdT_vAbyPDmJ8AwDOGRmgiyffJNW2JgWns3H3YWJyLyo532XeZunVZNOlq78L49DHe7-oTThEe1Y10Rxt4xA93lw_jO7yyfR2PLqa5JqBTHlBnoUWihJmDEitpS0NM1ZqRmtpBdOKWt6noDEtMbdKmNoSBQawrCmzdIhON3Nnwb_P-_uq1kVtmkZ1xs9jRQoJsiS8B_EG1MHHGIytZsG1KqwqDNX6S9WvL_XOyXa4ilo1NqhOu_gjikIQxmXPXW4411kfWrXwoamrpFaND18S_WuN_Ff_ZVVpmegnqhSMFA</recordid><startdate>20050401</startdate><enddate>20050401</enddate><creator>Kladeková, Daniela</creator><creator>Gálová, Miriam</creator><creator>Pikna, L'ubomír</creator><general>Taylor & Francis Group</general><general>Taylor & Francis</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20050401</creationdate><title>Voltammetric Investigation of the Oxidation of Iron Powder</title><author>Kladeková, Daniela ; Gálová, Miriam ; Pikna, L'ubomír</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c407t-82b6c6a324ee07cc7f9e4ef7c43d7f64ca3f53d70c13915fa6edf2a0e017d34f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Chemistry</topic><topic>Colloidal state and disperse state</topic><topic>electrochemical dissolution</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>iron</topic><topic>powder particles</topic><topic>Surface physical chemistry</topic><topic>voltammetry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kladeková, Daniela</creatorcontrib><creatorcontrib>Gálová, Miriam</creatorcontrib><creatorcontrib>Pikna, L'ubomír</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Particulate science and technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kladeková, Daniela</au><au>Gálová, Miriam</au><au>Pikna, L'ubomír</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Voltammetric Investigation of the Oxidation of Iron Powder</atitle><jtitle>Particulate science and technology</jtitle><date>2005-04-01</date><risdate>2005</risdate><volume>23</volume><issue>2</issue><spage>189</spage><epage>199</epage><pages>189-199</pages><issn>0272-6351</issn><eissn>1548-0046</eissn><coden>PTCHDS</coden><abstract>Voltammetry measurements were performed on iron powder particles of various size fractions immobilized on the surface of a paraffin-impregnated graphite electrode in electrolytes of various pH values. The course of voltammetric curves implies that the start of the dissolution process is shifted negatively with increasing pH value and the anodic dissolution process of iron is inhibited due to adsorption of products of the electrode reaction on iron particle surfaces. The rate of dissolution is changed also with iron particle size: decreasing dissolution rate and appearance of inhibition were encountered with an increase in particle size. A mechanism was suggested taking into account the influence of both pH of the electrolyte and particle size fraction. Electrochemical dissolution of freshly reduced iron from the solution proceeds at a lower potential than the same process of iron powder immobilized on the electrode.</abstract><cop>Washington, DC</cop><pub>Taylor & Francis Group</pub><doi>10.1080/02726350590922260</doi><tpages>11</tpages></addata></record> |
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subjects | Chemistry Colloidal state and disperse state electrochemical dissolution Exact sciences and technology General and physical chemistry iron powder particles Surface physical chemistry voltammetry |
title | Voltammetric Investigation of the Oxidation of Iron Powder |
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