<?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>S1870-249X2020000200117</article-id>
<article-id pub-id-type="doi">10.29356/jmcs.v64i2.1126</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Use of Chemically Modified Titanium Dioxide Particles to Mediate the Non-isothermal Cold Crystallization of Poly(latic acid)]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Mendoza]]></surname>
<given-names><![CDATA[Guadalupe]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Peña-Juárez]]></surname>
<given-names><![CDATA[M.G.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Gonzalez-Calderon]]></surname>
<given-names><![CDATA[J.A.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Pérez]]></surname>
<given-names><![CDATA[Elías]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad Autónoma de San Luis Potosí  ]]></institution>
<addr-line><![CDATA[ San Luis Potosí]]></addr-line>
<country>México</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Universidad Autónoma de San Luis Potosí  ]]></institution>
<addr-line><![CDATA[ San Luis Potosí]]></addr-line>
<country>México</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Universidad Autónoma de San Luis Potosí Instituto de Física ]]></institution>
<addr-line><![CDATA[ San Luis Potosí]]></addr-line>
<country>México</country>
</aff>
<aff id="Af4">
<institution><![CDATA[,Universidad Autónoma de San Luis Potosí Instituto de Física ]]></institution>
<addr-line><![CDATA[ San Luis Potosí]]></addr-line>
<country>México</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>06</month>
<year>2020</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>06</month>
<year>2020</year>
</pub-date>
<volume>64</volume>
<numero>2</numero>
<fpage>117</fpage>
<lpage>136</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1870-249X2020000200117&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1870-249X2020000200117&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1870-249X2020000200117&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract In this work, the effect of the chemical modification of titanium dioxide particles on the non-isothermal crystallization process of polylactic acid (PLA) was studied. Cold crystallization in some polymers occurs above the glass transition temperature (Tg) when the polymer chains gain sufficient mobility to organize themselves into the ordered structure (i.e. the crystal structure) by folding the chains. Cold crystallization in general is caused by the ordering of the molecular chains in the crystalline PLA due to the increased mobility during heating. Through an analysis of the cool crystallization process in DSC at different cooling rates, it was observed that the behavior of PLA and its composites made with titanium dioxide, neat and functionalized with dicarboxylic acids, can be described through the models used for crystallization of the polymer carrying out during cooling, such as Mo&#8217;s and Jeziorny&#8217;s model. In addition, it was determined that the chemical modification of TiO2 performed with silane increases the crystallization rate in the last step of the process; while the chemical modification with dicarboxylic acid has an accelerated effect on the crystal formation process attributed to the affinity between the aliphatic part of this group and the polymer chains. Also, it was shown that the inclusion of the silanized particles has no effect on the energy requirement compared to the pure PLA process; however, the addition of particles with the dicarboxylic acid decreases the energy value required to complete the crystalline state due to affinity at the surface to immobilize the polymer chains. Finally, it is emphasized that the activation energy required to perform the crystallization of PLA and its composites has positive values, which is an indicator that the crystallization was performed while heating, after reaching and passing the glass transition temperature and before melting.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen En este trabajo, se estudió el efecto de la modificación química de partículas de dióxido de titanio en el proceso de cristalización no isotérmica del ácido poliláctico (PLA). La cristalización en frío en algunos polímeros ocurre por encima de la temperatura de transición vítrea (Tg) cuando las cadenas de polímero ganan suficiente movilidad para organizarse en la estructura ordenada (es decir, la estructura cristalina) al doblar las cadenas. La cristalización en frío en general es causada por el ordenamiento de las cadenas moleculares en el PLA cristalino debido al aumento de la movilidad durante el calentamiento. A través de un análisis del proceso de cristalización en frío en DSC a diferentes velocidades de enfriamiento, se observó que el comportamiento del PLA y sus compuestos hechos con dióxido de titanio, puro y funcionalizado con ácidos dicarboxílicos, se puede describir a través de modelos utilizados para la cristalización de polímeros llevada a cabo durante el enfriamiento, como los Modelos de Mo y Jeziorny. Además, se determinó que la modificación química del TiO2 realizada con silano aumenta la velocidad de cristalización en el último paso del proceso; mientras que la modificación química con ácido dicarboxílico tiene un efecto acelerado en el proceso de formación de cristales, lo cual es atribuido a la afinidad entre la parte alifática de este grupo y las cadenas poliméricas. Además, se demostró que la inclusión de las partículas silanizadas no tiene efecto en el requerimiento de energía en comparación con el proceso de PLA puro; sin embargo, la adición de partículas con el ácido dicarboxílico disminuye el valor energético requerido para completar el estado cristalino debido a la afinidad en la superficie para inmovilizar las cadenas de polímero. Finalmente, se enfatiza que la energía de activación requerida para realizar la cristalización de PLA y sus compuestos tiene valores positivos, lo cual es un indicador de que la cristalización fue realizada durante el calentamiento, después de alcanzar y pasar la temperatura de transición vítrea, y antes de fundir.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Non-isothermal crystallization]]></kwd>
<kwd lng="en"><![CDATA[titanium dioxide]]></kwd>
<kwd lng="en"><![CDATA[composites]]></kwd>
<kwd lng="en"><![CDATA[chemical modification]]></kwd>
<kwd lng="en"><![CDATA[poly(lactic acid)]]></kwd>
<kwd lng="es"><![CDATA[Cristalización no-isotérmica]]></kwd>
<kwd lng="es"><![CDATA[dióxido de titanio]]></kwd>
<kwd lng="es"><![CDATA[compositos]]></kwd>
<kwd lng="es"><![CDATA[modificación química]]></kwd>
<kwd lng="es"><![CDATA[ácido poliláctico]]></kwd>
</kwd-group>
</article-meta>
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