<?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>0035-001X</journal-id>
<journal-title><![CDATA[Revista mexicana de física]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. mex. fis.]]></abbrev-journal-title>
<issn>0035-001X</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Mexicana de Física]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0035-001X2008000500004</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Thermally assisted NO2 and NH3 gas desorption process in a polyaniline thin film based optochemical sensor]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Elizalde-Torres]]></surname>
<given-names><![CDATA[J.]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Hu]]></surname>
<given-names><![CDATA[Hailin]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Guadarrama-Santana]]></surname>
<given-names><![CDATA[A.]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[García-Valenzuela]]></surname>
<given-names><![CDATA[A.]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Saniger]]></surname>
<given-names><![CDATA[J.M.]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,UNAM Centro de Investigación en Ciencias Aplicadas y Desarrollo Tecnológico ]]></institution>
<addr-line><![CDATA[México D.F.]]></addr-line>
<country>México</country>
</aff>
<aff id="A02">
<institution><![CDATA[,UNAM Centro de Investigación en Energía ]]></institution>
<addr-line><![CDATA[Temixco Morelos]]></addr-line>
<country>México</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>10</month>
<year>2008</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>10</month>
<year>2008</year>
</pub-date>
<volume>54</volume>
<numero>5</numero>
<fpage>358</fpage>
<lpage>363</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S0035-001X2008000500004&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S0035-001X2008000500004&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S0035-001X2008000500004&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[NO2 gas is a strong electron acceptor that can oxidize the chemically deposited semiconductor polyaniline (PANI) at room temperature under atmospheric pressure. Since each redox state of this polymer is associated with a specific electronic structure, an oxidized PANI thin film undergoes a color change that can be detected in a sensitive optochemical sensor. But the strongly absorbed NO2 molecules cannot be removed at room temperature from the polymer material during the purging process with a dried N2 gas flux. We report in this work that a heating element can be integrated into the optochemical sensor to elevate the sensing sample temperature during the desorption process. At temperatures higher than 50° C, the optical signal of the NO2 absorbed PANI samples starts to return to its original value during the purging process, suggesting the desorption of the NO2 species from the PANI samples. The higher the heating temperature, the greater the activation energy for desorption, and consequently the faster the desorption speed. Similar results are also obtained for the NH3 desorption process occurring in the same polymer.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[El gas NO2 es un fuerte aceptor de electrón que puede oxidar la película de polianilina (PANI) depositada químicamente a temperatura ambiente bajo presión atmosférica. Como cada estado de redox de este polímero está asociado con una estructura electrónica específica, el proceso de absorción de NO2 que ocurre en una película de PANI puede detectarse fácilmente por el cambio de su color en un sensor optoquímico. Sin embargo, se ha observado que las moléculas absorbidas de NO2 en PANI no se pueden remover fácilmente durante el proceso de purgación con un flujo seco de N2 a temperatura ambiente. En este trabajo se reporta que se pudo integrar un elemento de calentamiento dentro del sensor óptico para elevar la temperatura de la muestra de sensado durante el proceso de desorción. Se conoce que a temperaturas mayores que 50° C, la señal óptica de las muestras de PANI con moléculas de NO2 absorbidas empieza a regresar a su valor inicial durante el proceso de purgación, lo cual indica que las especies de NO2 están dejando a la película de PANI. Mientras más alta la temperatura de calentamiento, mayor será la energía de activación para la deserción, y consecuentemente más rápida será la velocidad de deserción. Resultados similares también se han obtenido con el proceso de adsorción-desorción de moléculas de NH3 en el mismo polímero.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Polyaniline thin films]]></kwd>
<kwd lng="en"><![CDATA[NO2 desorption process]]></kwd>
<kwd lng="en"><![CDATA[activation energy for desorption]]></kwd>
<kwd lng="en"><![CDATA[optochemical sensors]]></kwd>
<kwd lng="es"><![CDATA[Películas delgadas de polianilina]]></kwd>
<kwd lng="es"><![CDATA[proceso de desorción de NO2]]></kwd>
<kwd lng="es"><![CDATA[energía de activación para deserción]]></kwd>
<kwd lng="es"><![CDATA[sensores optoquímicos]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p align="justify"><font face="verdana" size="4">Investigaci&oacute;n</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="center"><font face="verdana" size="4"><b>Thermally assisted NO<sub>2</sub> and NH<sub>3</sub> gas desorption process in a polyaniline thin film based optochemical sensor</b></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="center"><font face="verdana" size="2"><b>J. Elizalde&#150;Torres&ordf;, Hailin Hu<sup>b,</sup>*, A. Guadarrama&#150;Santana&ordf;, A. Garc&iacute;a&#150;Valenzuela&ordf;, and J.M. Saniger&ordf;</b></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><i>&ordf; Centro de Investigaci&oacute;n en Ciencias Aplicadas y Desarrollo Tecnol&oacute;gico, UN AM, Circuito Exterior, Ciudad Universitaria, Coyoac&aacute;n, M&eacute;xico D.F. 04510, M&eacute;xico.</i></font></p>     <p align="justify"><font face="verdana" size="2"><i><sup>b</sup> Centro de Investigaci&oacute;n en Energ&iacute;a, UNAM, Av. Xochicalco S/N, Temixco, 62580, Morelos, M&eacute;xico.</i></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>*. Corresponding author:</b>     ]]></body>
<body><![CDATA[<br> e&#150;mail: <a href="mailto:hzh@cie.unam.mx">hzh@cie.unam.mx</a></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2">Recibido el 10 de septiembre de 2007    <br>   Aceptado el 4 de septiembre de 2008</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Abstract</b></font></p>     <p align="justify"><font face="verdana" size="2">NO<sub>2</sub> gas is a strong electron acceptor that can oxidize the chemically deposited semiconductor polyaniline (PANI) at room temperature under atmospheric pressure. Since each redox state of this polymer is associated with a specific electronic structure, an oxidized PANI thin film undergoes a color change that can be detected in a sensitive optochemical sensor. But the strongly absorbed NO<sub>2</sub> molecules cannot be removed at room temperature from the polymer material during the purging process with a dried N<sub>2</sub> gas flux. We report in this work that a heating element can be integrated into the optochemical sensor to elevate the sensing sample temperature during the desorption process. At temperatures higher than 50&deg; C, the optical signal of the NO<sub>2</sub> absorbed PANI samples starts to return to its original value during the purging process, suggesting the desorption of the NO<sub>2</sub> species from the PANI samples. The higher the heating temperature, the greater the activation energy for desorption, and consequently the faster the desorption speed. Similar results are also obtained for the NH<sub>3</sub> desorption process occurring in the same polymer.</font></p>     <p align="justify"><font face="verdana" size="2"><b>Keywords: </b>Polyaniline thin films; NO<sub>2</sub> desorption process; activation energy for desorption; optochemical sensors.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Resumen</b></font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">El gas NO<sub>2</sub> es un fuerte aceptor de electr&oacute;n que puede oxidar la pel&iacute;cula de polianilina (PANI) depositada qu&iacute;micamente a temperatura ambiente bajo presi&oacute;n atmosf&eacute;rica. Como cada estado de redox de este pol&iacute;mero est&aacute; asociado con una estructura electr&oacute;nica espec&iacute;fica, el proceso de absorci&oacute;n de NO<sub>2</sub> que ocurre en una pel&iacute;cula de PANI puede detectarse f&aacute;cilmente por el cambio de su color en un sensor optoqu&iacute;mico. Sin embargo, se ha observado que las mol&eacute;culas absorbidas de NO<sub>2</sub> en PANI no se pueden remover f&aacute;cilmente durante el proceso de purgaci&oacute;n con un flujo seco de N<sub>2</sub> a temperatura ambiente. En este trabajo se reporta que se pudo integrar un elemento de calentamiento dentro del sensor &oacute;ptico para elevar la temperatura de la muestra de sensado durante el proceso de desorci&oacute;n. Se conoce que a temperaturas mayores que 50&deg; C, la se&ntilde;al &oacute;ptica de las muestras de PANI con mol&eacute;culas de NO<sub>2</sub> absorbidas empieza a regresar a su valor inicial durante el proceso de purgaci&oacute;n, lo cual indica que las especies de NO<sub>2</sub> est&aacute;n dejando a la pel&iacute;cula de PANI. Mientras m&aacute;s alta la temperatura de calentamiento, mayor ser&aacute; la energ&iacute;a de activaci&oacute;n para la deserci&oacute;n, y consecuentemente m&aacute;s r&aacute;pida ser&aacute; la velocidad de deserci&oacute;n. Resultados similares tambi&eacute;n se han obtenido con el proceso de adsorci&oacute;n&#150;desorci&oacute;n de mol&eacute;culas de NH<sub>3</sub> en el mismo pol&iacute;mero.</font></p>     <p align="justify"><font face="verdana" size="2"><b>Descriptores: </b>Pel&iacute;culas delgadas de polianilina; proceso de desorci&oacute;n de NO<sub>2</sub>; energ&iacute;a de activaci&oacute;n para deserci&oacute;n; sensores optoqu&iacute;micos.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2">PACS: 71.20.Rv; 73.61.Ph; 78.40.Me; 78.66.Qn; 82.35.Cd</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><a href="/pdf/rmf/v54n5/v54n5a4.pdf" target="_blank">DESCARGAR ART&Iacute;CULO EN FORMATO PDF</a></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Acknowledgements</b></font></p>     <p align="justify"><font face="verdana" size="2">The authors wish to thank Mr. Mart&iacute;n Brise&ntilde;o for his technical assistance in the fabrication of the heating element. This work was financed by the Proyecto Universitario de Nanotecnolog&iacute;a (IMPULSA), UNAM and CONACyT&#150;M&eacute;xico (42794).</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     ]]></body>
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