<?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>S0872-19042005000400004</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Electrochemical Behaviour of Copper Nitroprusside Generated in situ Onto the Graphite Paste Electrode Surface, and its Application in the Determination of N-Acethylcysteine]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Carmo]]></surname>
<given-names><![CDATA[D. Ribeiro do]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Silva]]></surname>
<given-names><![CDATA[R. Moutinho da]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Stradiotto]]></surname>
<given-names><![CDATA[N. Ramos]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,UNESP-Universidade Estadual Paulista Departamento de Física e Química ]]></institution>
<addr-line><![CDATA[Ilha Solteira SP]]></addr-line>
<country>Brazil</country>
</aff>
<aff id="A02">
<institution><![CDATA[,Universidade Estadual Paulista (UNESP) Instituto de Química de Araraquara ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>00</month>
<year>2005</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>00</month>
<year>2005</year>
</pub-date>
<volume>23</volume>
<numero>4</numero>
<fpage>457</fpage>
<lpage>470</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_arttext&amp;pid=S0872-19042005000400004&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_abstract&amp;pid=S0872-19042005000400004&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_pdf&amp;pid=S0872-19042005000400004&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Copper nitroprusside (CuNP) was generated on the graphite paste electrode using a new methodology of the preparation. The electrochemical studies were carried out by cyclic voltammetry technique. The cyclic voltammogram of the modified electrode, CuNP showed two redox couples (E0’)1=0.22 and (E0’)2=0.88 V vs. SCE attributed to Cu(I)/Cu(II) and Fe(II)(CN)5NO/Fe(III)(CN)5NO, respectively. The nature of the cation affect the (E0’)1 and (E0’)2, as current intensity, shifting the E0’ for more positive potentials, for two redox processes. The voltammograms obtained with different KCl concentrations (0.1-3.0 mol L-1) exhibit a shift in the (E0’)1 to more positive potentials; this change was linear with the supporting electrolyte concentrations change. It was verified that the (E0’)1 remained practically constant at pH between 6 and 3. However, a new process with (E0’)3 (0.48 V) appears at pH<3 and it was ascribed to formation of intermediary species. The redox couple at (E0’)2=0.88 V presents an electrocatalytic response for N-acethylcysteine. The modified graphite paste electrode gives a linear response between 5.0´10-4 to 1.0´10-2 mol L-1 of N-acethylcysteine with a detection limit of 4.5´10-4 (±5%) mol L-1 (n=3) and an amperometric sensitivity of 4.9 mA/mmol L-1. The electrocatalytic oxidation of N-acethylcysteine compounds by the mediator has been used for the determination of N-acethylcysteine in a commercially pharmaceutical available product.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[copper nitroprusside]]></kwd>
<kwd lng="en"><![CDATA[modified electrode]]></kwd>
<kwd lng="en"><![CDATA[electrocatalysis]]></kwd>
<kwd lng="en"><![CDATA[N- acethylcysteine]]></kwd>
<kwd lng="en"><![CDATA[oxidation]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p class=MsoNormal align=center style='text-align:center'><b>Electrochemical Behaviour of Copper Nitroprusside Generated <i>in situ</i> Onto the Graphite Paste Electrode Surface, and its Application in the Determination of N-Acethylcysteine</b><b></b></p>      <p class=MsoNormal align=center style='text-align:center'><b>&nbsp;</b><b>&nbsp;</b></p>      <p class=MsoBodyText align=center><b>D. Ribeiro do Carmo,<a name="top1"></a><a href="#1">*</a>    R. Moutinho da Silva,<sup>1</sup> N. Ramos Stradiotto<sup>1</sup></b></p>      <p class=MsoBodyText align=center><i>&nbsp;</i></p>      <p class=MsoNormal align=center style='text-align:center'><i>Departamento de Física e Química, UNESP-Universidade Estadual Paulista, Av. Brasil, 56-Centro, C. P. 31, 15385-000 Ilha Solteira- SP,  Brazil </i></p>      <p class=MsoNormal align=center style='text-align:center'><i><sup>1</sup></i><b><i> </i></b><i>Instituto de Química de Araraquara, Universidade Estadual Paulista (UNESP) CP 355, 14801-970 Araraquara &#8211;SP,</i><i> Brazil</i></p>      <p class=MsoBodyText align=center><i>&nbsp;</i></p>      <p>&nbsp;</p>      <p><b>Abstract</b></p>      <p>Copper nitroprusside (CuNP) was generated on the graphite paste electrode using    a new methodology of the preparation. The electrochemical studies were carried    out bycyclic voltammetry technique. The cyclic voltammogram of the modified    electrode, CuNP showed two redox couples (E<sup>0&#8217;</sup>)<sub>1</sub>=0.22    and (E<sup>0&#8217;</sup>)<sub>2</sub>=0.88 V <i>vs.</i> SCE attributed to Cu<sup>(I)</sup>/Cu<sup>(II)</sup>    and Fe<sup>(II)</sup>(CN)<sub>5</sub>NO/Fe<sup>(III)</sup>(CN)<sub>5</sub>NO,    respectively. The nature of the cation affect the (E<sup>0&#8217;</sup>)<sub>1</sub>    and (E<sup>0&#8217;</sup>)<sub>2</sub>, as current intensity, shifting the E<sup>0&#8217;</sup>    for more positive potentials, for two redox processes. The voltammograms obtained    with different KCl concentrations (0.1-3.0 mol L<sup>-1</sup>) exhibit a shift    in the (E<sup>0&#8217;</sup>)<sub>1</sub> to more positive potentials; this    change was linear with the supporting electrolyte concentrations change. It    was verified that the (E<sup>0&#8217;</sup>)<sub>1</sub> remained practically    constant at pH between 6 and 3. However, a new process with (E<sup>0&#8217;</sup>)<sub>3</sub>    (0.48 V) appears at pH&lt;3 and it was ascribed to formation of intermediary    species. </p>     ]]></body>
<body><![CDATA[<p>The redox couple at (E<sup>0&#8217;</sup>)<sub>2</sub>=0.88 V presents an electrocatalytic    response for N-acethylcysteine. The modified graphite paste electrode gives    a linear response between5.0´10<sup>-4</sup> to 1.0´10<sup>-2</sup> mol L<sup>-1</sup>    of N-acethylcysteine with a detection limit of 4.5´10<sup>-4</sup> (±5%) mol    L<sup>-1</sup> (n=3) and an amperometric sensitivity of 4.9 mA/mmol L<sup>-1</sup>.  </p>     <p>The electrocatalytic oxidation of N-acethylcysteine compounds by the mediator    has been used for the determination of N-acethylcysteine in a commercially pharmaceutical    available product. </p>     <p>&nbsp;</p>     <p><b>Keywords:</b> copper nitroprusside, modified electrode, electrocatalysis, N- acethylcysteine, oxidation.</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>      ]]></body>
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<body><![CDATA[<p>&nbsp;</p>       <p><a name="1"></a><a href="#top1">*</a> Corresponding author. E-mail address:    <a href="mailto:docarmo@fqm.feis.unesp.br">docarmo@fqm.feis.unesp.br</a> </p>         ]]></body><back>
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