<?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>S0035-001X2013000300002</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Evaluación de la estructura y microestructura de óxidos de Ni xMg1-xO, obtenidos por co-precipitación]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Martínez-Lozano]]></surname>
<given-names><![CDATA[G.]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Kryshtab]]></surname>
<given-names><![CDATA[T.]]></given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Hesiquio-Garduño]]></surname>
<given-names><![CDATA[M.]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Kryvko]]></surname>
<given-names><![CDATA[A.]]></given-names>
</name>
<xref ref-type="aff" rid="A03"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Instituto Politécnico Nacional Departamento de Física ]]></institution>
<addr-line><![CDATA[México D.F.]]></addr-line>
<country>México</country>
</aff>
<aff id="A02">
<institution><![CDATA[,Instituto Politécnico Nacional Departamento de Ingeniería Química Petrolera ]]></institution>
<addr-line><![CDATA[México D.F.]]></addr-line>
<country>México</country>
</aff>
<aff id="A03">
<institution><![CDATA[,Instituto Politécnico Nacional Departamento de Sistemas ]]></institution>
<addr-line><![CDATA[México D.F.]]></addr-line>
<country>México</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>06</month>
<year>2013</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>06</month>
<year>2013</year>
</pub-date>
<volume>59</volume>
<numero>3</numero>
<fpage>186</fpage>
<lpage>190</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S0035-001X2013000300002&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S0035-001X2013000300002&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S0035-001X2013000300002&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Los óxidos de Ni xMg1-xO, se prepararon mediante tratamiento térmico a temperaturas de 400, 600 y 800°C del precursor tipo hidrotalcita obtenidos por el método de co-precipitación a pH constante. Los óxidos obtenidos, fueron caracterizados mediante difracción de rayos X. Con los resultados obtenidos, se concluye que los óxidos calcinados a temperaturas de 400° C y 600° C son inestables al mantener el efecto de memoria y con tiempo regresan al precursor. La incorporación de Ni al oxido de Mg le proporciona estabilidad a los compuestos al tratarlos térmicamente a 800°C. Para analizar la estructura y microestructura, se usan las reflexiones 111, 200 y 220. Las posiciones de los máximos de los picos de difracción están deslizadas a ángulos grandes de 2&#952;, con respecto a las posiciones simuladas para MgO y NiO, esto significa la existencia de esfuerzos compresivos o vacancias. Los parámetros de la microestructura (tamaño de dominio coherente y microdeformación) fueron evaluados, hallándose que el tamaño de dominio coherente se encuentra en el rango de 8-10 nm y la presencia de los esfuerzos residuales de microdeformación es posible asociar con la existencia de los defectos extendidos.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Ni xMg1-xO oxides were prepared by thermal treatment at temperatures of 400°C, 600°C and 800°C from a hydrotalcite-like precursor obtained by co-precipitation at constant pH. The oxides obtained were characterized by X-ray diffraction methods. From the obtained results we concluded that the oxides calcined at temperatures of 400° C and 600° C are unstable that means that there exists the effect of memory and with a time they return to the precursor. Presence of Ni in Mg oxide provides stability of the compounds thermally treated at 800°C. In order to analyze the structure and microstructure, the reflections 111,200 and 220 were used. The positions of the maxima of the diffraction peaks are shifted with respect to the simulated ones for MgO and NiO. This result reveals that in solid solutions studied compressive strains or vacation are present. The parameters of the microstructure (coherent domain size and microdeformations) were evaluated. The coherent domain size was found to be in the range of 8 - 10 nm and the presence of residual strains of microdeformation can be associated with the existence of extended defects]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Difracción de rayos X]]></kwd>
<kwd lng="es"><![CDATA[dominio coherente]]></kwd>
<kwd lng="es"><![CDATA[microdeformación]]></kwd>
<kwd lng="es"><![CDATA[hidrotalcita]]></kwd>
<kwd lng="en"><![CDATA[X-ray diffraction]]></kwd>
<kwd lng="en"><![CDATA[coherent domain]]></kwd>
<kwd lng="en"><![CDATA[microdeformations]]></kwd>
<kwd lng="en"><![CDATA[hydrotalcite]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[  	    <p align="justify"><font face="verdana" size="4">Research</font></p>  	    <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>  	    <p align="center"><font face="verdana" size="4"><b>Evaluaci&oacute;n de la estructura y microestructura de &oacute;xidos de Ni<sub>x</sub>Mg<sub>1&#45;x</sub>O, obtenidos por co&#45;precipitaci&oacute;n</b></font></p>  	    <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>  	    <p align="center"><font face="verdana" size="2"><b>G. Mart&iacute;nez&#45;Lozano*, T. Kryshtab*, M. Hesiquio&#45;Gardu&ntilde;o** y A. Kryvko***</b></font></p>  	    <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>  	    <p align="justify"><font face="verdana" size="2"><i>* Departamento de F&iacute;sica, ESFM, Instituto Polit&eacute;cnico Nacional, UPALM, Av. IPNs/n, Edif. 9, 07738, M&eacute;xico, D.F. M&eacute;xico, e&#45;mail:</i> <a href="mailto:marloz7@yahoo.com.mx">marloz7@yahoo.com.mx</a>; <a href="mailto:tkrysh@esfm.ipn.mx">tkrysh@esfm.ipn.mx</a></font></p>  	    <p align="justify"><font face="verdana" size="2"><i>** Departamento de Ingenier&iacute;a Qu&iacute;mica Petrolera, ESIQIE, Instituto Polit&eacute;cnico Nacional, UPALM, Av. IPNs/n, Edif 6, 07738 M&eacute;xico, D.F. M&eacute;xico.</i></font></p>  	    <p align="justify"><font face="verdana" size="2"><i>*** Departamento de Sistemas, ESIME, Instituto Polit&eacute;cnico Nacional, UPALM, Av. IPNs/n, Edif. Z&#45;4, 07738, M&eacute;xico D.F., M&eacute;xico.</i></font></p>  	    ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">&nbsp;</font></p>  	    <p align="justify"><font face="verdana" size="2">Received 10 August 2012;    <br> 	Accepted 28 November 2012</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 &oacute;xidos de Ni<sub>x</sub>Mg<sub>1&#45;x</sub>O, se prepararon mediante tratamiento t&eacute;rmico a temperaturas de 400, 600 y 800&deg;C del precursor tipo hidrotalcita obtenidos por el m&eacute;todo de co&#45;precipitaci&oacute;n a pH constante. Los &oacute;xidos obtenidos, fueron caracterizados mediante difracci&oacute;n de rayos X. Con los resultados obtenidos, se concluye que los &oacute;xidos calcinados a temperaturas de 400&deg; C y 600&deg; C son inestables al mantener el efecto de memoria y con tiempo regresan al precursor. La incorporaci&oacute;n de Ni al oxido de Mg le proporciona estabilidad a los compuestos al tratarlos t&eacute;rmicamente a 800&deg;C. Para analizar la estructura y microestructura, se usan las reflexiones 111, 200 y 220. Las posiciones de los m&aacute;ximos de los picos de difracci&oacute;n est&aacute;n deslizadas a &aacute;ngulos grandes de 2<i>&#952;</i>, con respecto a las posiciones simuladas para MgO y NiO, esto significa la existencia de esfuerzos compresivos o vacancias. Los par&aacute;metros de la microestructura (tama&ntilde;o de dominio coherente y microdeformaci&oacute;n) fueron evaluados, hall&aacute;ndose que el tama&ntilde;o de dominio coherente se encuentra en el rango de 8&#45;10 nm y la presencia de los esfuerzos residuales de microdeformaci&oacute;n es posible asociar con la existencia de los defectos extendidos.</font></p>  	    <p align="justify"><font face="verdana" size="2"><b>Descriptores:</b> Difracci&oacute;n de rayos X; dominio coherente; microdeformaci&oacute;n; hidrotalcita.</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">Ni<sub>x</sub>Mg<sub>1&#45;x</sub>O oxides were prepared by thermal treatment at temperatures of 400&deg;C, 600&deg;C and 800&deg;C from a hydrotalcite&#45;like precursor obtained by co&#45;precipitation at constant pH. The oxides obtained were characterized by X&#45;ray diffraction methods. From the obtained results we concluded that the oxides calcined at temperatures of 400&deg; C and 600&deg; C are unstable that means that there exists the effect of memory and with a time they return to the precursor. Presence of Ni in Mg oxide provides stability of the compounds thermally treated at 800&deg;C. In order to analyze the structure and microstructure, the reflections 111,200 and 220 were used. The positions of the maxima of the diffraction peaks are shifted with respect to the simulated ones for MgO and NiO. This result reveals that in solid solutions studied compressive strains or vacation are present. The parameters of the microstructure (coherent domain size and microdeformations) were evaluated. The coherent domain size was found to be in the range of 8 &#45; 10 nm and the presence of residual strains of microdeformation can be associated with the existence of extended defects.</font></p>  	    ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2"><b>Keywords:</b> X&#45;ray diffraction; coherent domain; microdeformations; hydrotalcite.</font></p>  	    <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>  	    <p align="justify"><font face="verdana" size="2">PACS: 81.20.Fw; 61.72.Dd</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/v59n3/v59n3a2.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>Referencias</b></font></p>  	    <!-- ref --><p align="justify"><font face="verdana" size="2">1. M. M&uuml;ller, and K. 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