Influence of H2SO4 concentration on the mechanism of the processes and on the electrochemical activity of the Pb/PbO2/PbSO4 electrode
The aim of the present investigation is to study the influence of H2SO4 concentration on the electrochemical activity, the phase composition and the structure and morphology of the PbO2 particles. The study is performed through cycling (between 700 and 1600 mV versus Hg/Hg2SO4 electrode) of a Pb/PbO...
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Veröffentlicht in: | Journal of power sources 2004-10, Vol.137 (2), p.288-308 |
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description | The aim of the present investigation is to study the influence of H2SO4 concentration on the electrochemical activity, the phase composition and the structure and morphology of the PbO2 particles. The study is performed through cycling (between 700 and 1600 mV versus Hg/Hg2SO4 electrode) of a Pb/PbO2/PbSO4 electrode immersed in sulfuric acid solutions of various concentrations (ranging within 2 orders of magnitude: 6.0-0.05 M H2SO4). In this concentration region, sulfuric acid dissociates in two steps resulting in the formation of HSO4- and SO42- ions, respectively. It has been established experimentally that the electrochemical activity of the PbO2/PbSO4 electrode depends on the concentration of HSO4- ions in the solution. Three acid concentration regions can be distinguished: (a) active acid concentration region (5.O M > CH2SO4 > 0.5M), where the concentration of HSO4- ions is the highest and a betaPbO2 phase is formed; PbO2 particles are drop-like in shape and contain large hydrated (gel) zones; the electrode has the highest capacity; (b) passive high concentration region (CH.S04 > 5.0 M), where the concentration of HSO4- ions decreases at the expense of formation of H2 SO4 molecules; crystal-shaped cxPbO2 particles are formed; the capacity of the electrode declines; (c) passive low concentration region (CH2S04 < 0.5 M), where the concentration of HS04- ions decreases at the expense of the formation of SO42- ions; the content of aPbO2 in the anodic layer increases; PbO2 particles are crystal-shaped and are interconnected in dendrites; the capacity of the electrode declines. The above electrochemical behavior of the PbO2/PbSO4 electrode is explained by the mechanism of the reactions in the gel zones of the PbO2 particles and by the influence of HSO4- ions on the number of electrochemically active particles. On grounds of the obtained experimental results it has been established that the working interval within which the CH2SO4 may change on cycling is from 5.0 to 1.5 M, i.e. 3.5 M H2SO4 per 1 1 of H2SO4 solution with s.g. 1.28 takes part in the reactions on both battery plates. This is the maximum amount of H2SO4 in the solution that would have no detrimental effect on the positive plates of the lead-acid battery. |
doi_str_mv | 10.1016/j.jpowsour.2004.06.006 |
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The study is performed through cycling (between 700 and 1600 mV versus Hg/Hg2SO4 electrode) of a Pb/PbO2/PbSO4 electrode immersed in sulfuric acid solutions of various concentrations (ranging within 2 orders of magnitude: 6.0-0.05 M H2SO4). In this concentration region, sulfuric acid dissociates in two steps resulting in the formation of HSO4- and SO42- ions, respectively. It has been established experimentally that the electrochemical activity of the PbO2/PbSO4 electrode depends on the concentration of HSO4- ions in the solution. Three acid concentration regions can be distinguished: (a) active acid concentration region (5.O M > CH2SO4 > 0.5M), where the concentration of HSO4- ions is the highest and a betaPbO2 phase is formed; PbO2 particles are drop-like in shape and contain large hydrated (gel) zones; the electrode has the highest capacity; (b) passive high concentration region (CH.S04 > 5.0 M), where the concentration of HSO4- ions decreases at the expense of formation of H2 SO4 molecules; crystal-shaped cxPbO2 particles are formed; the capacity of the electrode declines; (c) passive low concentration region (CH2S04 < 0.5 M), where the concentration of HS04- ions decreases at the expense of the formation of SO42- ions; the content of aPbO2 in the anodic layer increases; PbO2 particles are crystal-shaped and are interconnected in dendrites; the capacity of the electrode declines. The above electrochemical behavior of the PbO2/PbSO4 electrode is explained by the mechanism of the reactions in the gel zones of the PbO2 particles and by the influence of HSO4- ions on the number of electrochemically active particles. On grounds of the obtained experimental results it has been established that the working interval within which the CH2SO4 may change on cycling is from 5.0 to 1.5 M, i.e. 3.5 M H2SO4 per 1 1 of H2SO4 solution with s.g. 1.28 takes part in the reactions on both battery plates. This is the maximum amount of H2SO4 in the solution that would have no detrimental effect on the positive plates of the lead-acid battery.</description><identifier>ISSN: 0378-7753</identifier><identifier>EISSN: 1873-2755</identifier><identifier>DOI: 10.1016/j.jpowsour.2004.06.006</identifier><identifier>CODEN: JPSODZ</identifier><language>eng</language><publisher>Lausanne: Elsevier Sequoia</publisher><subject>Applied sciences ; Direct energy conversion and energy accumulation ; Electrical engineering. Electrical power engineering ; Electrical power engineering ; Electrochemical conversion: primary and secondary batteries, fuel cells ; Energy ; Energy. Thermal use of fuels ; Equipments for energy generation and conversion: thermal, electrical, mechanical energy, etc ; Exact sciences and technology ; Fuel cells</subject><ispartof>Journal of power sources, 2004-10, Vol.137 (2), p.288-308</ispartof><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1619-701f9c8b2a1780a9fe69f638fa7c33f81a429e32966a31e31417f2b599eecfa23</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16548252$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>PAVLOV, D</creatorcontrib><creatorcontrib>KIRCHEV, A</creatorcontrib><creatorcontrib>STOYCHEVA, M</creatorcontrib><creatorcontrib>MONAHOV, B</creatorcontrib><title>Influence of H2SO4 concentration on the mechanism of the processes and on the electrochemical activity of the Pb/PbO2/PbSO4 electrode</title><title>Journal of power sources</title><description>The aim of the present investigation is to study the influence of H2SO4 concentration on the electrochemical activity, the phase composition and the structure and morphology of the PbO2 particles. The study is performed through cycling (between 700 and 1600 mV versus Hg/Hg2SO4 electrode) of a Pb/PbO2/PbSO4 electrode immersed in sulfuric acid solutions of various concentrations (ranging within 2 orders of magnitude: 6.0-0.05 M H2SO4). In this concentration region, sulfuric acid dissociates in two steps resulting in the formation of HSO4- and SO42- ions, respectively. It has been established experimentally that the electrochemical activity of the PbO2/PbSO4 electrode depends on the concentration of HSO4- ions in the solution. Three acid concentration regions can be distinguished: (a) active acid concentration region (5.O M > CH2SO4 > 0.5M), where the concentration of HSO4- ions is the highest and a betaPbO2 phase is formed; PbO2 particles are drop-like in shape and contain large hydrated (gel) zones; the electrode has the highest capacity; (b) passive high concentration region (CH.S04 > 5.0 M), where the concentration of HSO4- ions decreases at the expense of formation of H2 SO4 molecules; crystal-shaped cxPbO2 particles are formed; the capacity of the electrode declines; (c) passive low concentration region (CH2S04 < 0.5 M), where the concentration of HS04- ions decreases at the expense of the formation of SO42- ions; the content of aPbO2 in the anodic layer increases; PbO2 particles are crystal-shaped and are interconnected in dendrites; the capacity of the electrode declines. The above electrochemical behavior of the PbO2/PbSO4 electrode is explained by the mechanism of the reactions in the gel zones of the PbO2 particles and by the influence of HSO4- ions on the number of electrochemically active particles. On grounds of the obtained experimental results it has been established that the working interval within which the CH2SO4 may change on cycling is from 5.0 to 1.5 M, i.e. 3.5 M H2SO4 per 1 1 of H2SO4 solution with s.g. 1.28 takes part in the reactions on both battery plates. This is the maximum amount of H2SO4 in the solution that would have no detrimental effect on the positive plates of the lead-acid battery.</description><subject>Applied sciences</subject><subject>Direct energy conversion and energy accumulation</subject><subject>Electrical engineering. Electrical power engineering</subject><subject>Electrical power engineering</subject><subject>Electrochemical conversion: primary and secondary batteries, fuel cells</subject><subject>Energy</subject><subject>Energy. Thermal use of fuels</subject><subject>Equipments for energy generation and conversion: thermal, electrical, mechanical energy, etc</subject><subject>Exact sciences and technology</subject><subject>Fuel cells</subject><issn>0378-7753</issn><issn>1873-2755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNpFkN9KwzAUh4MoOKevIL3Ru3b50ybNpQx1g8EG6nVIsxOW0qaz6ZQ9gO9tihtCOCEn3y8nfAjdE5wRTPiszup99x26Q59RjPMM8wxjfoEmpBQspaIoLtEEM1GmQhTsGt2EUGOMCRF4gn6W3jYH8AaSziYL-rbOE9PFox96PbjOJ3ENO0haMDvtXWhHbmzs-85ACBAS7bdnChowQ7zYQeuMbhJtBvflhuM5tKlmm2pNYxkHnegt3KIrq5sAd6d9ij5ent_ni3S1fl3On1apIZzIVGBipSkrqokosZYWuLSclVYLw5gtic6pBEYl55oRYCQnwtKqkBLAWE3ZFD3-vRs__3mAMKjWBQNNoz10h6BoSbkUUkaQ_4Gm70Lowap971rdHxXBarSuanW2rkbrCnMVrcfgw2mCDlGA7bU3LvyneZGXtKDsF13OhoU</recordid><startdate>20041029</startdate><enddate>20041029</enddate><creator>PAVLOV, D</creator><creator>KIRCHEV, A</creator><creator>STOYCHEVA, M</creator><creator>MONAHOV, B</creator><general>Elsevier Sequoia</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20041029</creationdate><title>Influence of H2SO4 concentration on the mechanism of the processes and on the electrochemical activity of the Pb/PbO2/PbSO4 electrode</title><author>PAVLOV, D ; KIRCHEV, A ; STOYCHEVA, M ; MONAHOV, B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1619-701f9c8b2a1780a9fe69f638fa7c33f81a429e32966a31e31417f2b599eecfa23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Applied sciences</topic><topic>Direct energy conversion and energy accumulation</topic><topic>Electrical engineering. Electrical power engineering</topic><topic>Electrical power engineering</topic><topic>Electrochemical conversion: primary and secondary batteries, fuel cells</topic><topic>Energy</topic><topic>Energy. Thermal use of fuels</topic><topic>Equipments for energy generation and conversion: thermal, electrical, mechanical energy, etc</topic><topic>Exact sciences and technology</topic><topic>Fuel cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>PAVLOV, D</creatorcontrib><creatorcontrib>KIRCHEV, A</creatorcontrib><creatorcontrib>STOYCHEVA, M</creatorcontrib><creatorcontrib>MONAHOV, B</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Electronics & Communications 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 power sources</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>PAVLOV, D</au><au>KIRCHEV, A</au><au>STOYCHEVA, M</au><au>MONAHOV, B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Influence of H2SO4 concentration on the mechanism of the processes and on the electrochemical activity of the Pb/PbO2/PbSO4 electrode</atitle><jtitle>Journal of power sources</jtitle><date>2004-10-29</date><risdate>2004</risdate><volume>137</volume><issue>2</issue><spage>288</spage><epage>308</epage><pages>288-308</pages><issn>0378-7753</issn><eissn>1873-2755</eissn><coden>JPSODZ</coden><abstract>The aim of the present investigation is to study the influence of H2SO4 concentration on the electrochemical activity, the phase composition and the structure and morphology of the PbO2 particles. The study is performed through cycling (between 700 and 1600 mV versus Hg/Hg2SO4 electrode) of a Pb/PbO2/PbSO4 electrode immersed in sulfuric acid solutions of various concentrations (ranging within 2 orders of magnitude: 6.0-0.05 M H2SO4). In this concentration region, sulfuric acid dissociates in two steps resulting in the formation of HSO4- and SO42- ions, respectively. It has been established experimentally that the electrochemical activity of the PbO2/PbSO4 electrode depends on the concentration of HSO4- ions in the solution. Three acid concentration regions can be distinguished: (a) active acid concentration region (5.O M > CH2SO4 > 0.5M), where the concentration of HSO4- ions is the highest and a betaPbO2 phase is formed; PbO2 particles are drop-like in shape and contain large hydrated (gel) zones; the electrode has the highest capacity; (b) passive high concentration region (CH.S04 > 5.0 M), where the concentration of HSO4- ions decreases at the expense of formation of H2 SO4 molecules; crystal-shaped cxPbO2 particles are formed; the capacity of the electrode declines; (c) passive low concentration region (CH2S04 < 0.5 M), where the concentration of HS04- ions decreases at the expense of the formation of SO42- ions; the content of aPbO2 in the anodic layer increases; PbO2 particles are crystal-shaped and are interconnected in dendrites; the capacity of the electrode declines. The above electrochemical behavior of the PbO2/PbSO4 electrode is explained by the mechanism of the reactions in the gel zones of the PbO2 particles and by the influence of HSO4- ions on the number of electrochemically active particles. On grounds of the obtained experimental results it has been established that the working interval within which the CH2SO4 may change on cycling is from 5.0 to 1.5 M, i.e. 3.5 M H2SO4 per 1 1 of H2SO4 solution with s.g. 1.28 takes part in the reactions on both battery plates. This is the maximum amount of H2SO4 in the solution that would have no detrimental effect on the positive plates of the lead-acid battery.</abstract><cop>Lausanne</cop><pub>Elsevier Sequoia</pub><doi>10.1016/j.jpowsour.2004.06.006</doi><tpages>21</tpages></addata></record> |
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subjects | Applied sciences Direct energy conversion and energy accumulation Electrical engineering. Electrical power engineering Electrical power engineering Electrochemical conversion: primary and secondary batteries, fuel cells Energy Energy. Thermal use of fuels Equipments for energy generation and conversion: thermal, electrical, mechanical energy, etc Exact sciences and technology Fuel cells |
title | Influence of H2SO4 concentration on the mechanism of the processes and on the electrochemical activity of the Pb/PbO2/PbSO4 electrode |
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