<?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>1870-249X</journal-id>
<journal-title><![CDATA[Journal of the Mexican Chemical Society]]></journal-title>
<abbrev-journal-title><![CDATA[J. Mex. Chem. Soc]]></abbrev-journal-title>
<issn>1870-249X</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Química de México A.C.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1870-249X2010000300004</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Spectroscopic Determination of Optimal Hydration Time of Zircon Surface]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ordóñez-Regil]]></surname>
<given-names><![CDATA[Eduardo]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[García-Rosales]]></surname>
<given-names><![CDATA[Genoveva]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[García-González]]></surname>
<given-names><![CDATA[Nidia]]></given-names>
</name>
<xref ref-type="aff" rid="A03"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Instituto Nacional de Investigaciones Nucleares Departamento de Química ]]></institution>
<addr-line><![CDATA[La Marquesa Ocoyoacac]]></addr-line>
<country>México</country>
</aff>
<aff id="A02">
<institution><![CDATA[,Instituto Tecnológico de Toluca División de Estudios de Post-Grado ]]></institution>
<addr-line><![CDATA[Metepec Estado de México]]></addr-line>
<country>México</country>
</aff>
<aff id="A03">
<institution><![CDATA[,Universidad Autónoma del Estado de México Facultad de Química ]]></institution>
<addr-line><![CDATA[Toluca Estado de México]]></addr-line>
<country>México</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>09</month>
<year>2010</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>09</month>
<year>2010</year>
</pub-date>
<volume>54</volume>
<numero>3</numero>
<fpage>153</fpage>
<lpage>156</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1870-249X2010000300004&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1870-249X2010000300004&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1870-249X2010000300004&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[When a mineral surface is immersed in an aqueous solution, it develops an electric charge produced by the amphoteric dissociation of hydroxyl groups created by the hydration of the solid surface. This is one influential surface property. The complete hydration process takes a time which is specific for each mineral species. The knowledge of the aqueous solution contact time for complete surface hydration is mandatory for further surface phenomena studies. This study deals with the optimal hydration time of the raw zircon (ZrSiO4) surface comparing the classical potentiometric titrations with a fluorescence spectroscopy technique. The latter is easy and reliable as it demands only one sample batch to determine the optimal time to ensure a total hydration of the zircon surface. The analytical results of neutron activation analysis (NAA) showed the presence of trace quantities of Dy3+, Eu3+ and Er³ in the bulk of zircon. The Dy3+ is structured in the zircon crystalline lattice and undergoes the same chemical reactions as zircon. Furthermore, the Dy3+ has a good fluorescent response whose intensity is enhanced by hydration molecules. The results show that, according to the potentiometric analysis, the hydration process for each batch (at least 8 sample batches) takes around 2 h, while the spectrometric method indicates only 5 min from only one batch. Both methods showed that the zircon surface have a 16h optimal hydration time.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Los minerales que son inmersos en solución acuosa, desarrollan una carga eléctrica, producida por la aparición de la disociación anfotérica de los grupos hidroxilo formados en superficie. Esta propiedad es específica para cada mineral y la determinación del tiempo de hidratación es fundamental para realizar posteriores estudios de sorción en la interfase sólido/líquido. En este estudio se determinó el tiempo óptimo de hidratación del circón (ZrSiO4), comparando la técnica clásica por titulación potenciométrica con la técnica de fluorescencia a diferentes tiempos. La técnica de fluorescencia fue desarrollada gracias a las impurezas de tierras raras que son contenidas en cantidades traza en los minerales de circón. El análisis por activación neutrónica mostró que las impurezas contenidas en este lote de circón eran principalmente el Dy3+, Eu3+ y el Er3+. El Dy3+ tiene una buena respuesta fluorescente que se incrementa con las moléculas de agua a medida que este elemento se hidrata. Los resultados mostraron que el método potenciométrico es largo y tedioso, pues se requiere un lote por cada tiempo en estudio y toma alrededor de 2 h el análisis, en tanto que el método espectroscópico requiere de una sola muestra que se analiza puntualmente pasado el tiempo requerido, esto sólo toma 5 min, después del cual se continua con el proceso de hidratación. Ámbos métodos mostraron que la superficie del circón requiere de 16 h para alcanzar el tiempo óptimo de hidratación.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Hydration]]></kwd>
<kwd lng="en"><![CDATA[Dysprosium]]></kwd>
<kwd lng="en"><![CDATA[Zircon]]></kwd>
<kwd lng="en"><![CDATA[Fluorescence]]></kwd>
<kwd lng="es"><![CDATA[Hidratación]]></kwd>
<kwd lng="es"><![CDATA[disprosio]]></kwd>
<kwd lng="es"><![CDATA[circón]]></kwd>
<kwd lng="es"><![CDATA[fluorescencia]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p align="justify"><font face="verdana" size="4">Article</font></p>     <p align="center"><font face="verdana" size="2">&nbsp;</font></p>     <p align="center"><font face="verdana" size="4"><b>Spectroscopic Determination of Optimal Hydration Time of Zircon Surface</b></font></p>     <p align="center"><font face="verdana" size="2">&nbsp;</font></p>     <p align="center"><font face="verdana" size="2"><b>Eduardo Ord&oacute;&ntilde;ez&#150;Regil<sup>1*</sup>, Genoveva Garc&iacute;a&#150;Rosales<sup>1,</sup> <sup>2</sup> and Nidia Garc&iacute;a&#150;Gonz&aacute;lez<sup>3</sup></b></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><i><sup>1</sup> Departamento de Qu&iacute;mica., Instituto Nacional de Investigaciones Nucleares. Carretera M&eacute;xico&#150;Toluca S/N, km. 36.5. La Marquesa, Ocoyoacac, M&eacute;xico. <sup>*</sup>Responsible author:</i> <a href="mailto:eduardo.ordonez@inin.gob.mx">eduardo.ordonez@inin.gob.mx</a>.</font></p>     <p align="justify"><font face="verdana" size="2"><i><sup>2</sup> Divisi&oacute;n de Estudios de Post&#150;Grado, Instituto Tecnol&oacute;gico de Toluca. Ex Rancho la Virgen s/n, Metepec, Estado de M&eacute;xico, M&eacute;xico.</i></font></p>     <p align="justify"><font face="verdana" size="2"><i><sup>3</sup> Facultad de Qu&iacute;mica, Universidad Aut&oacute;noma del Estado de M&eacute;xico. Av. C. Col&oacute;n y Av. Tollocan, Toluca, Estado de M&eacute;xico, M&eacute;xico.</i></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">Received November 10, 2009    <br>   Accepted May 7, 2010</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">When a mineral surface is immersed in an aqueous solution, it develops an electric charge produced by the amphoteric dissociation of hydroxyl groups created by the hydration of the solid surface. This is one influential surface property. The complete hydration process takes a time which is specific for each mineral species. The knowledge of the aqueous solution contact time for complete surface hydration is mandatory for further surface phenomena studies. This study deals with the optimal hydration time of the raw zircon (ZrSiO<sub>4</sub>) surface comparing the classical potentiometric titrations with a fluorescence spectroscopy technique. The latter is easy and reliable as it demands only one sample batch to determine the optimal time to ensure a total hydration of the zircon surface. The analytical results of neutron activation analysis (NAA) showed the presence of trace quantities of Dy<sup>3+</sup>, Eu<sup>3+</sup> and Er<sup>3</sup> in the bulk of zircon. The Dy<sup>3+</sup> is structured in the zircon crystalline lattice and undergoes the same chemical reactions as zircon. Furthermore, the Dy<sup>3+</sup> has a good fluorescent response whose intensity is enhanced by hydration molecules. The results show that, according to the potentiometric analysis, the hydration process for each batch (at least 8 sample batches) takes around 2 h, while the spectrometric method indicates only 5 min from only one batch. Both methods showed that the zircon surface have a 16h optimal hydration time.</font></p>     <p align="justify"><font face="verdana" size="2"><b>Keywords: </b>Hydration, Dysprosium, Zircon, Fluorescence.</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>     <p align="justify"><font face="verdana" size="2">Los minerales que son inmersos en soluci&oacute;n acuosa, desarrollan una carga el&eacute;ctrica, producida por la aparici&oacute;n de la disociaci&oacute;n anfot&eacute;rica de los grupos hidroxilo formados en superficie. Esta propiedad es espec&iacute;fica para cada mineral y la determinaci&oacute;n del tiempo de hidrataci&oacute;n es fundamental para realizar posteriores estudios de sorci&oacute;n en la interfase s&oacute;lido/l&iacute;quido. En este estudio se determin&oacute; el tiempo &oacute;ptimo de hidrataci&oacute;n del circ&oacute;n (ZrSiO<sub>4</sub>), comparando la t&eacute;cnica cl&aacute;sica por titulaci&oacute;n potenciom&eacute;trica con la t&eacute;cnica de fluorescencia a diferentes tiempos. La t&eacute;cnica de fluorescencia fue desarrollada gracias a las impurezas de tierras raras que son contenidas en cantidades traza en los minerales de circ&oacute;n. El an&aacute;lisis por activaci&oacute;n neutr&oacute;nica mostr&oacute; que las impurezas contenidas en este lote de circ&oacute;n eran principalmente el Dy<sup>3+</sup>, Eu<sup>3+</sup> y el Er<sup>3+</sup>. El Dy<sup>3+</sup> tiene una buena respuesta fluorescente que se incrementa con las mol&eacute;culas de agua a medida que este elemento se hidrata. Los resultados mostraron que el m&eacute;todo potenciom&eacute;trico es largo y tedioso, pues se requiere un lote por cada tiempo en estudio y toma alrededor de 2 h el an&aacute;lisis, en tanto que el m&eacute;todo espectrosc&oacute;pico requiere de una sola muestra que se analiza puntualmente pasado el tiempo requerido, esto s&oacute;lo toma 5 min, despu&eacute;s del cual se continua con el proceso de hidrataci&oacute;n. &Aacute;mbos m&eacute;todos mostraron que la superficie del circ&oacute;n requiere de 16 h para alcanzar el tiempo &oacute;ptimo de hidrataci&oacute;n.</font></p>     <p align="justify"><font face="verdana" size="2"><b>Palabras clave: </b>Hidrataci&oacute;n, disprosio, circ&oacute;n, fluorescencia.</font></p>     ]]></body>
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