<?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>0120-2804</journal-id>
<journal-title><![CDATA[Revista Colombiana de Química]]></journal-title>
<abbrev-journal-title><![CDATA[Rev.Colomb.Quim.]]></abbrev-journal-title>
<issn>0120-2804</issn>
<publisher>
<publisher-name><![CDATA[Departamento de Química,  Universidad Nacional de Colombia.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0120-28042021000200049</article-id>
<article-id pub-id-type="doi">10.15446/rev.colomb.quim.v50n2.89644</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Síntesis del hidróxido de níquel (II) con disolución multicomponente de la lixiviación de sulfuro de la tecnología Caron]]></article-title>
<article-title xml:lang="en"><![CDATA[Nickel hydroxide (II) synthesis with sulfide leaching multi-element solution from Caron technology]]></article-title>
<article-title xml:lang="pt"><![CDATA[Síntese de hidróxido de níquel (II) com solução de lixiviação de sulfetos multicomponentes da Caron technology]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Cisneros-Sánchez]]></surname>
<given-names><![CDATA[Deisy]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Otero-Calvi]]></surname>
<given-names><![CDATA[Alexis]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Quesada-González]]></surname>
<given-names><![CDATA[Omaida]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Sosa-Martínez]]></surname>
<given-names><![CDATA[Mercedes]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Capote-Flores]]></surname>
<given-names><![CDATA[Neicis]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Centro de Investigaciones del Níquel  ]]></institution>
<addr-line><![CDATA[Moa Holguín]]></addr-line>
<country>Cuba</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Universidad de Moa Departamento de Metalurgia-Química Facultad de Metalurgia y Electromecánica]]></institution>
<addr-line><![CDATA[Moa Holguín]]></addr-line>
<country>Cuba</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Universidad de Oriente Departamento de Química, Facultad de Ciencias Naturales y Exactas ]]></institution>
<addr-line><![CDATA[Santiago de Cuba ]]></addr-line>
<country>Cuba</country>
</aff>
<aff id="Af4">
<institution><![CDATA[,Centro de Investigaciones del Níquel  ]]></institution>
<addr-line><![CDATA[Moa Holguín]]></addr-line>
<country>Cuba</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>08</month>
<year>2021</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>08</month>
<year>2021</year>
</pub-date>
<volume>50</volume>
<numero>2</numero>
<fpage>49</fpage>
<lpage>57</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_arttext&amp;pid=S0120-28042021000200049&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_abstract&amp;pid=S0120-28042021000200049&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_pdf&amp;pid=S0120-28042021000200049&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen Se determinaron las condiciones más favorables para la síntesis de hidróxido de níquel (II) por precipitación química a partir de la disolución lixiviada del sulfuro de níquel de la tecnología Caron. La disolución lixiviada de fuerza iónica igual a 4,6 mol-L-1 fue tratada con hidróxidos de amonio y sodio. Se calcularon las propiedades termodinámicas como entalpía, entropía y energía libre y se construyeron diagramas de zona de predominancia. Se demostró la conveniencia de realizar el proceso a 303 K, pH entre 11 y13 y concentración de amoníaco de 0,5 a 1,0 mol&#8226;L-1. En estas condiciones fueron obtenidas altas eficiencias de precipitación de los cationes metálicos de la disolución inicial. El sólido precipitado se caracterizó mediante espectrometría de absorción atómica y difracción de rayos X. Se obtuvo un beta-hidróxido de níquel (II) con la siguiente composición química: 58,5 &#8804; Ni &#8804; 59,1%, 1,7 &#8804; Co &#8804; 2,1%, 0,5 &#8804; Fe &#8804; 0,6%, Cu, Zn, Mn y Mg &#8804; 0,2%.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract The most favorable conditions for the synthesis of nickel (II) hydroxide were determined by chemical precipitation, from the leached solution of nickel sulfide from the Caron technology. The leached solution with an ionic strength equal to 4.6 mol-L-1 was treated with ammonium and sodium hydroxides. Thermodynamic properties such as enthalpy, entropy, and free energy were calculated and predominance zone diagrams were constructed. The convenience of performing the process at 303 K, pH between 11 and 13, and ammonia concentration of 0.5 to 1.0 mol&#8226;L-1 was demonstrated. Under these conditions, high precipitation efficiencies of the metal cations from the initial solution were obtained. The precipitated solid was characterized by atomic absorption spectrometry and X-ray diffraction. Nickel (II) beta-hydroxide with the following chemical composition was obtained: 58.5 &#8804; Ni &#8804; 59.1%, 1.7 &#8804; Co &#8804; 2.1%, 0.5 &#8804; Fe &#8804; 0.6%, Cu, Zn, Mn and Mg &#8804; 0.2%.]]></p></abstract>
<abstract abstract-type="short" xml:lang="pt"><p><![CDATA[Resumo As condições mais favoráveis para a síntese do hidróxido de níquel (II) foram determinadas por precipitação química, a partir da solução lixiviada de sulfeto de níquel da tecnologia Caron. A solução lixiviada de força iônica igual a 4,6 mol-L-1, foi tratada com hidróxidos de amônio e sódio. Foram calculadas propriedades termodinâmicas, como entalpia, entropia e energia livre, e diagramas de zonas de predominância foram construídos. Foi demonstrada a conveniência de realizar o processo a 303 K, pH entre 11 e 13 e concentração de amônia de 0,5 a 1,0 mol&#8226;L-1. Nessas condições, foram obtidas altas eficiências de precipitação dos cátions metálicos da solução inicial. O sólido precipitado foi caracterizado por espectrometria de absorção atômica e difração de raios-x. Foi obtido beta-hidróxido de níquel (II) com a seguinte composição química: 58,5 &#8804; Ni &#8804; 59,1%, 1,7 &#8804; Co &#8804; 2,1%, 0,5 &#8804; Fe &#8804; 0,6%, Cu , Zn, Mn e Mg &#8804; 0,2%.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[precipitación química]]></kwd>
<kwd lng="es"><![CDATA[beta-hidróxido de níquel]]></kwd>
<kwd lng="es"><![CDATA[diagrama de predominancia]]></kwd>
<kwd lng="en"><![CDATA[Chemical precipitation]]></kwd>
<kwd lng="en"><![CDATA[nickel beta hydroxide]]></kwd>
<kwd lng="en"><![CDATA[predominance diagram]]></kwd>
<kwd lng="pt"><![CDATA[Precipitação química]]></kwd>
<kwd lng="pt"><![CDATA[hidróxido de níquel beta]]></kwd>
<kwd lng="pt"><![CDATA[diagrama de dominância]]></kwd>
</kwd-group>
</article-meta>
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