<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>0872-1904</journal-id>
<journal-title><![CDATA[Portugaliae Electrochimica Acta]]></journal-title>
<abbrev-journal-title><![CDATA[Port. Electrochim. Acta]]></abbrev-journal-title>
<issn>0872-1904</issn>
<publisher>
<publisher-name><![CDATA[Sociedade Portuguesa de Electroquímica]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0872-19042006000300006</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Active/passive transition of niobium in strong acid and alkaline solutions]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Mickova]]></surname>
<given-names><![CDATA[Irena]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Abdurauf]]></surname>
<given-names><![CDATA[Prusi]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Grcev]]></surname>
<given-names><![CDATA[Toma]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Arsov]]></surname>
<given-names><![CDATA[Ljubomir]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,University St. Cyril and Methodius Faculty of Technology and Metallurgy ]]></institution>
<addr-line><![CDATA[Skopje ]]></addr-line>
<country>Republic of Macedonia</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>00</month>
<year>2006</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>00</month>
<year>2006</year>
</pub-date>
<volume>24</volume>
<numero>3</numero>
<fpage>377</fpage>
<lpage>385</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_arttext&amp;pid=S0872-19042006000300006&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_abstract&amp;pid=S0872-19042006000300006&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_pdf&amp;pid=S0872-19042006000300006&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[By cyclic voltammetry the active/passive transition of Nb electrode has been investigated in concentration range from 0.1 M to 10 M aqueous solutions of H2SO4 and KOH. Results indicate the strong influence of the concentration and electrolyte nature to the active/passive transitions and stability of passive films. Depending on electrolyte concentrations, at potential of 1 V the calculated thickness of passive films varied from 2.2 nm to 3.2 nm. For the same concentrations of H2SO4 and KOH the formed passive films in KOH are thicker than in H2SO4. By multiple cycle sequences in which the final anodic potential is gradually enlarged, the barrier properties of passive films on Nb electrode were confirmed. In the first positive scan after the active/passive transition, no cathodic or reactivation peaks for both 1 M H2SO4 and KOH were observed. Only for higher concentrations of KOH (> 2 M) the small reactivation process was recorded. In concentration of 5 M and 10 M KOH, if after the passive film formation the Nb electrodes were maintained for 15 min at cathodic potential of -1.55 (SHE), the cyclic voltammograms indicated the complete dissolution of passive films. The voltammetric data have confirmed that the Nb electrode is more resistant in concentrated H2SO4 than in concentrated KOH solutions.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[niobium]]></kwd>
<kwd lng="en"><![CDATA[passivity]]></kwd>
<kwd lng="en"><![CDATA[cyclic voltammetry]]></kwd>
<kwd lng="en"><![CDATA[reactivation]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p align="center"><b>Active/passive transition of niobium in strong </b><b>acid    and alkaline solutions </b></p>     <p align="center"><b>Irena Mickova, Prusi Abdurauf, Toma Grcev, Ljubomir Arsov<a href="#1">*</a><a name="top1"></a></b></p>     <p align="center"><i>Faculty of Technology and Metallurgy, University &#8220;St. Cyril    and Methodius&#8221;, </i><i>1000 </i><i>Skopje</i><i>,    </i><i>Republic</i><i> of </i><i>    Macedonia</i></p>     <p></p>      <p>&nbsp;</p>      <p>&nbsp;</p>      <p><b>Abstract</b></p>      <p align="justify">By cyclic voltammetry the active/passive transition of Nb electrode    has been investigated in concentration range from 0.1 M to 10 M aqueous solutions    of H<sub>2</sub>SO<sub>4 </sub>and KOH. Results indicate the strong influence    of the concentration and electrolyte nature to the active/passive transitions    and stability of passive films.</p>     <p align="justify">Depending on electrolyte concentrations, at potential of 1    V the calculated thickness of passive films varied from 2.2 nm to 3.2 nm. For    the same concentrations of H<sub>2</sub>SO<sub>4</sub> and KOH the formed passive    films in KOH are thicker than in H<sub>2</sub>SO<sub>4</sub>.</p>     <p align="justify">By multiple cycle sequences in which the final anodic potential    is gradually enlarged, the barrier properties of passive films on Nb electrode    were confirmed. </p>     ]]></body>
<body><![CDATA[<p align="justify">In the first positive scan after the active/passive transition,    no cathodic or reactivation peaks for both 1 M H<sub>2</sub>SO<sub>4 </sub>and    KOH were observed. Only for higher concentrations of KOH (&gt; 2 M) the small    reactivation process was recorded. In concentration of 5 M and 10 M KOH, if    after the passive film formation the Nb electrodes were maintained for 15 min    at cathodic potential of -1.55 (SHE), the cyclic voltammograms indicated  the    complete dissolution of passive films. The voltammetric data have confirmed    that the Nb electrode is more resistant in concentrated H<sub>2</sub>SO<sub>4</sub>    than in concentrated KOH solutions.</p>      <p><b><i>Keywords: </i></b>niobium, passivity, cyclic voltammetry, reactivation.</p>      <p >&nbsp;</p>      <p >&nbsp;</p>      <p >Texto disponível em PDF</p>      <p>Full text only in PDF format</p>      <p >&nbsp;</p>      <p >&nbsp;</p>      <p ><b>References</b></p>      <!-- ref --><p>1. I. Arsova, A. Prusi and Lj. Arsov, <i>J. Solid State Electrochem</i>. 7 (2003) 217-222.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000022&pid=S0872-1904200600030000600001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><p>2. T. Hurlen, H. Bentzen, S. Hornkjo, <i>Electrochim</i><i>. Acta</i> 32 (1987) 1613-1617.</p>      <p  >3. K. Hensler, M. Schulze, <i>Electrochim</i><i>. Acta</i> 20 (1975) 237-244.</p>      <p>4 . I. Uehera, T. Sakai, H. Ishikawa, H. Takenaka, <i>Corrosion </i>45 (7) (1989) 548-553.</p>      <p>5. A. Prusi and Lj. Arsov, <i>Corrosion Sci</i>. 3(1) (1991) 153-164. </p>      <p>6. A. Prusi, Lj. Arsov, B. Popov, B. Haran, <i>J. Electrochem. </i><i>Soc</i>. 149 (11) (2001) B491-B498. </p>      <p>7.  F. Di Quarto, S. Piazza, C. Sunseri, <i>Electrochim. Acta</i> 35(1) (1990) 99-107.</p>      <p>8. G.E. Cavigliasso, M.J. Esplandiu, V.A. Macagno, <i>J. Appl. Electrochem</i>. 28 (1998) 1213-1219.</p>      <p >9. M. Edilberg, D. Sandulor, <i >Electrokhimiya </i>23(4) (1985) 533-535.</p>      <p >10. K. Sugimoto, G. Belanger, D. Piron, <i >J. Electrochem. Soc</i>. 126(4) (1979), 535-541.</p>      <p >11. A.G. Gad Allah, <i>J. Appl. </i><i>Electrochem</i>. 21 (1991) 346-351.</p>      ]]></body>
<body><![CDATA[<p>12. W.A. Badawy, A. Gad-Allah, H. Rehan, <i>J. Appl. Electrochem</i>. 17 (1987) 559-566.</p>      <p>13. I. Arsova, A. Prusi, T. Grcev, Lj. Arsov, <i>J. Serb. Chem. Soc</i>. 2 (2006) (in-press).</p>      <p>14. I. Mickova, A. Prusi, T. Grcev, Lj. Arsov, <i>Croat. Chim. Acta</i> (accepted). </p>      <p >&nbsp;</p>      <p ><a href="#top1">*</a><a name="1"></a>Corresponding author. E-mail address:    <a href="mailto:arsov@ukim.edu.mk">arsov@ukim.edu.mk</a></p>       ]]></body><back>
<ref-list>
<ref id="B1">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Arsova]]></surname>
<given-names><![CDATA[I.]]></given-names>
</name>
<name>
<surname><![CDATA[Prusi]]></surname>
<given-names><![CDATA[A.]]></given-names>
</name>
<name>
<surname><![CDATA[Arsov]]></surname>
<given-names><![CDATA[Lj.]]></given-names>
</name>
</person-group>
<source><![CDATA[J. Solid State Electrochem]]></source>
<year>2003</year>
<numero>7</numero>
<issue>7</issue>
<page-range>217-222</page-range></nlm-citation>
</ref>
</ref-list>
</back>
</article>
