<?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>0188-4999</journal-id>
<journal-title><![CDATA[Revista internacional de contaminación ambiental]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. Int. Contam. Ambient]]></abbrev-journal-title>
<issn>0188-4999</issn>
<publisher>
<publisher-name><![CDATA[Universidad Nacional Autónoma de México, Instituto de Ciencias de la Atmósfera y Cambio Climático]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0188-49992019000200459</article-id>
<article-id pub-id-type="doi">10.20937/rica.2019.35.02.16</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[COMBINED TREATMENT USING OZONE FOR CYANIDE REMOVAL FROM WASTEWATER: A COMPARISON]]></article-title>
<article-title xml:lang="es"><![CDATA[TRATAMIENTO COMBINADO CON EL USO DE OZONO PARA LA REMOCIÓN DE CIANURO DE EFLUENTES: UNA COMPARACIÓN]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Morillo Esparza]]></surname>
<given-names><![CDATA[Jefferson]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Cevallos Cueva]]></surname>
<given-names><![CDATA[Nicolás]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Sandoval Pauker]]></surname>
<given-names><![CDATA[Christian]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Vargas Jentzsch]]></surname>
<given-names><![CDATA[Paul]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Muñoz Bisesti]]></surname>
<given-names><![CDATA[Florinella]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Escuela Politécnica Nacional Facultad de Ingeniería Química y Agroindustria Departamento de Ciencias Nucleares]]></institution>
<addr-line><![CDATA[Quito ]]></addr-line>
<country>Ecuador</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>00</month>
<year>2019</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>00</month>
<year>2019</year>
</pub-date>
<volume>35</volume>
<numero>2</numero>
<fpage>459</fpage>
<lpage>467</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S0188-49992019000200459&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S0188-49992019000200459&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S0188-49992019000200459&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[ABSTRACT Cyanidation is widely used by several gold mining companies worldwide. Since its wastewaters contain cyanide, appropriate treatments must be applied to remove this pollutant. Combinations of ozone (O3), hydrogen peroxide (H2O2) and activated carbon (AC) can be used for this purpose. In this work, synthetic cyanide solutions ([CN¯]o = 15.37 mM) were treated using O3 and the combinations O3/H2O2, O3/AC and O3/H2O2/AC under alkaline conditions. O3 was produced from dry oxygen at a rate of 2.51 g O3/h ([O3] gas-phase = 6.9x10-2 g/L). The concentration of cyanide (CN¯) and O3 consumption were measured and the performance of the treatments evaluated. The highest cyanide removal was reached at pH 11.0 for all cases and with 10 mg H2O2/mg O3 upon adding H2O2. In contrast, the addition of AC did not improve the cyanide removal in comparison with O3 alone. The best cyanide removal was achieved with the combination O3/H2O2 followed by the combination O3/H2O2/AC. Moreover, cyanidation effluents were treated using the combination O3/H2O2. In this case, almost a total removal of free cyanide was achieved after 3 min of treatment.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[RESUMEN El proceso de cianuración es ampliamente utilizado en la industria minera alrededor del mundo. Las aguas residuales de este proceso contienen cianuro, lo cual obliga al uso de tratamientos apropiados para su remoción. Para ello, se pueden utilizar combinaciones de ozono (O3), peróxido de hidrógeno (H2O2) y carbón activado (CA). En este trabajo se trataron, soluciones sintéticas de cianuro ([CN¯]o = 15.37 mM) con el uso de O3 y las combinaciones O3/H2O2, O3/CA y O3/H2O2/CA en condiciones alcalinas. Se produjo O3 a partir de oxígeno seco con una producción de 2.51 g O3/h ([O3] fase gaseosa = 6.9x10-2 g/L). Se evaluó el comportamiento de cada proceso y se midió la concentración de cianuro (CN¯) y el consumo de ozono durante los tratamientos. La mayor remoción de cianuro se alcanzó a pH 11.0 para todos los casos. Al añadir H2O2 la remoción fue mayor al usar 10 mg H2O2/mg O3. Por otra parte, la adición de CA no aumentó la remoción de cianuro en comparación al tratamiento sólo con O2. La mejor remoción de cianuro fue alcanzada con la combinación O3/H2O2 seguida de la combinación O3/H2O2/AC. Posteriormente, se trataron efluentes del proceso de cianuración con la combinación O3/H2O2. En este caso, se requirieron 3 min de tratamiento para la remoción total del cianuro libre.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[ozonation]]></kwd>
<kwd lng="en"><![CDATA[hydrogen peroxide]]></kwd>
<kwd lng="en"><![CDATA[peroxone process]]></kwd>
<kwd lng="en"><![CDATA[activated carbon]]></kwd>
<kwd lng="en"><![CDATA[cyanidation]]></kwd>
<kwd lng="es"><![CDATA[ozonificación]]></kwd>
<kwd lng="es"><![CDATA[peróxido de hidrógeno]]></kwd>
<kwd lng="es"><![CDATA[sistema peroxona]]></kwd>
<kwd lng="es"><![CDATA[carbón activado]]></kwd>
<kwd lng="es"><![CDATA[cianuración]]></kwd>
</kwd-group>
</article-meta>
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