<?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>0122-5383</journal-id>
<journal-title><![CDATA[CT&F - Ciencia, Tecnología y Futuro]]></journal-title>
<abbrev-journal-title><![CDATA[C.T.F Cienc. Tecnol. Futuro]]></abbrev-journal-title>
<issn>0122-5383</issn>
<publisher>
<publisher-name><![CDATA[Instituto Colombiano del Petróleo (ICP) - ECOPETROL S.A.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0122-53832009000100012</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[SYNGAS OBTAINMENT FROM THE GASIFICATION OF ASPHALTENES OF THE SAN FERNANDO CRUDE OIL]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Smith Moreno-Arciniegas]]></surname>
<given-names><![CDATA[Laura]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rodríguez-Corredor]]></surname>
<given-names><![CDATA[Fabio-Ernesto]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Afanador-Rey]]></surname>
<given-names><![CDATA[Luz-Edelmira]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Grosso-Vargas]]></surname>
<given-names><![CDATA[Jorge-Luis]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Ecopetrol S.A-Instituto Colombiano del Petróleo  ]]></institution>
<addr-line><![CDATA[Bucaramanga Santander]]></addr-line>
<country>Colombia</country>
</aff>
<aff id="A02">
<institution><![CDATA[,Universidad Industrial de Santander (UIS)  ]]></institution>
<addr-line><![CDATA[Bucaramanga Santander]]></addr-line>
<country>Colombia</country>
</aff>
<pub-date pub-type="pub">
<day>01</day>
<month>12</month>
<year>2009</year>
</pub-date>
<pub-date pub-type="epub">
<day>01</day>
<month>12</month>
<year>2009</year>
</pub-date>
<volume>3</volume>
<numero>5</numero>
<fpage>189</fpage>
<lpage>202</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_arttext&amp;pid=S0122-53832009000100012&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_abstract&amp;pid=S0122-53832009000100012&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_pdf&amp;pid=S0122-53832009000100012&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[In this work, we developed the first study in Colombia to obtain and evaluate syngas compositions derived from asphaltenes gasification. These asphaltenes came from the implementation of a Deasphalting process to San Fernando crude oil, with the purpose of looking for technological options for their utilization. We performed the design, installation and commissioning of facilities for the gasification of asphaltenes at laboratory scale, it following an experimental methodology, performing nine tests and considering temperature and agent gasification quantity (oxygen) as independent variables. The syngas derived from gasification was analyzed by two chromatographic techniques, which reported the presence of refinery gases and sulfur. We evidenced a growth tendency of CO, H2 and sulfur composition and a decrease in CH4 and CO2 composition with temperature. The composition of the syngas was evaluated with different quantities of gasification agent (33%, 40% and 47% the amount of oxygen theoretically required for complete combustion) at each temperature levels operated. It was established that when using a 40% of gasification agent, you get greater average content of CO and H2, which are the interest gases in the gasification process.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[En este trabajo se desarrolló el primer estudio en el país de la obtención y evaluación de las composiciones del syngas a partir de la gasificación de asfaltenos provenientes de la aplicación del proceso de Desasfaltado al crudo San Fernando, con el objeto de evaluar opciones tecnológicas para su utilización. Para ello se realizó el diseño y puesta en marcha de un sistema de gasificación de asfaltenos a escala de laboratorio, donde se empleó una metodología experimental, realizando nueve pruebas y tomando como variables independientes la temperatura y el agente gasificante (oxígeno). El syngas obtenido de la gasificación fue analizado por dos técnicas de cromatografía, las cuales reportaron la presencia de gases de refinería y azufrados. De estos resultados experimentales se evidencia una tendencia de crecimiento en la composición del CO, H2 y azufrados, y una disminución en la composición del CH4 y CO2 con la temperatura. Se evaluó la composición del syngas con la variación del agente gasificante (33%, 40% y 47% del oxígeno teórico requerido en una combustión total) en cada uno de los niveles de temperatura operados y se estableció que al utilizar un 40% de agente gasificante, se obtienen en promedio los mejores resultados en las composiciones del CO y H4, siendo estos los gases de interés en el proceso de gasificación.]]></p></abstract>
<abstract abstract-type="short" xml:lang="pt"><p><![CDATA[Neste trabalho desenvolveuse o primeiro estudo no país da obtenção e avaliação das composições do syngas a partir da gaseificação de asfaltenos provenientes da aplicação do processo de Desasfaltado ao cru São Fernando, com o objeto de avaliar opções tecnológicas para a sua utilização. Para tal realizou-se o desenho e posta em marcha de um sistema de gaseificação de asfaltenos a escala de laboratório, onde se empregou uma metodologia experimental, realizando nove provas e tomando como variáveis independentes a temperatura e o agente gaseificante (oxigênio). O syngas obtido da gaseificação foi analisado por duas técnicas de cromatografia, as quais reportaram a presença de gases de refinaria e enxofrados. Destes resultados experimentais evidenciase uma tendência de crescimento na composição do CO, H2 e enxofrados, e uma diminuição na composição do CH4 e CO2 com a temperatura. Avaliouse a composição do syngas com a variação do agente gaseificante (33%, 40% e 47% do oxigênio teórico requerido em uma combustão total) em cada um dos níveis de temperatura operados e estabeleceuse que ao utilizar um 40% de agente gaseificante, obtém-se em média os melhores resultados nas composições do CO e H4, sendo estes os gases de interesse no processo de gaseificação.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[San Fernando crude oil]]></kwd>
<kwd lng="en"><![CDATA[gasification]]></kwd>
<kwd lng="en"><![CDATA[asphaltenes]]></kwd>
<kwd lng="en"><![CDATA[syngas]]></kwd>
<kwd lng="es"><![CDATA[crudo San Fernando]]></kwd>
<kwd lng="es"><![CDATA[gasificación]]></kwd>
<kwd lng="es"><![CDATA[asfaltenos]]></kwd>
<kwd lng="es"><![CDATA[syngas.]]></kwd>
<kwd lng="pt"><![CDATA[cru São Fernando]]></kwd>
<kwd lng="pt"><![CDATA[gaseificação]]></kwd>
<kwd lng="pt"><![CDATA[asfaltenos]]></kwd>
<kwd lng="pt"><![CDATA[syngas]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[  <font face="Verdana" size="3"> <font size="4">    <p align="center"><b>SYNGAS OBTAINMENT FROM THE GASIFICATION OF ASPHALTENES OF THE     SAN FERNANDO CRUDE OIL</b></p></font> <font size="2">    <p align="center"><b>Laura-Smith Moreno-Arciniegas<sup>2*</sup>, Fabio-Ernesto Rodr&iacute;guez-Corredor<sup>2*</sup>, Luz-Edelmira Afanador-Rey<sup>1*</sup> and Jorge-Luis Grosso-Vargas<sup>2</sup></b></p>      <p align="center"><sup>1</sup> Ecopetrol S.A-Instituto Colombiano del Petr&oacute;leo,   P. O. Box 4185, Bucaramanga, Santander,  Colombia    <br>   <sup>2</sup> Universidad Industrial de Santander (UIS),  Bucaramanga,  Santander, Colombia  </p>        <p align="center">e-mail: <a href="mailto:luze.afanador@ecopetrol.com.co">luze.afanador@ecopetrol.com.co</a>&nbsp;&nbsp; e-mail:   <a href="mailto:laurasmith.moreno@gmail.com">laurasmith.moreno@gmail.com</a>&nbsp;     <br>e-mail: <a href="mailto:fabio.rodriguez.corredor@gmail.com">fabio.rodriguez.corredor@gmail.com</a></p>        <p align="center">(<i>Received April 30, 2008; Accepted July 17, 2009)</i></p>      <p align="center"><i>* To whom correspondence may be addressed</i></p></font>  <hr>     <p><b>ABSTRACT</b></p>     ]]></body>
<body><![CDATA[<p>In this work, we developed the   first study in Colombia to obtain and evaluate syngas compositions derived from   asphaltenes gasification. These asphaltenes came from the implementation of a   Deasphalting process to San Fernando crude oil, with the purpose of looking for   technological options for their utilization. We performed the design,   installation and commissioning of facilities for the gasification of   asphaltenes at laboratory scale, it following an experimental methodology,   performing nine tests and considering temperature and agent gasification   quantity (oxygen) as independent variables. The syngas derived from   gasification was analyzed by two chromatographic techniques, which reported the   presence of refinery gases and sulfur. We evidenced a growth tendency of CO, H<sub>2</sub>&nbsp;and   sulfur composition and a decrease in CH<sub>4</sub>&nbsp;and CO<sub>2</sub>&nbsp;composition   with temperature. The composition of the syngas was evaluated with different   quantities of gasification agent (33%, 40% and 47% the amount of oxygen   theoretically required for complete combustion) at each temperature levels   operated. It was established that when using a 40% of gasification agent, you   get greater average content of CO and H<sub>2</sub>, which are the interest   gases in the gasification process. </p>     <p><i><b>Keywords:</b> San Fernando crude   oil, gasification, asphaltenes, syngas.</i></p> <hr>     <p><b>RESUMEN</b></p>     <p>En este trabajo se desarroll&oacute; el   primer estudio en el pa&iacute;s de la obtenci&oacute;n y evaluaci&oacute;n de las composiciones del   syngas a partir de la gasificaci&oacute;n de asfaltenos provenientes de la aplicaci&oacute;n   del proceso de Desasfaltado al crudo San Fernando, con el objeto de evaluar   opciones tecnol&oacute;gicas para su utilizaci&oacute;n. Para ello se realiz&oacute; el dise&ntilde;o y   puesta en marcha de un sistema de gasificaci&oacute;n de asfaltenos a escala de   laboratorio, donde se emple&oacute; una metodolog&iacute;a experimental, realizando nueve   pruebas y tomando como variables independientes la temperatura y el agente   gasificante (ox&iacute;geno). El syngas obtenido de la gasificaci&oacute;n fue analizado por   dos t&eacute;cnicas de cromatograf&iacute;a, las cuales reportaron la presencia de gases de   refiner&iacute;a y azufrados. De estos resultados experimentales se evidencia una   tendencia de crecimiento en la composici&oacute;n del CO, H<sub>2</sub>&nbsp; y   azufrados, y una disminuci&oacute;n en la composici&oacute;n del CH<sub>4</sub>&nbsp;y CO<sub>2</sub>&nbsp;   con la temperatura. Se evalu&oacute; la&nbsp; composici&oacute;n del syngas con la variaci&oacute;n   del agente gasificante&nbsp; (33%, 40% y 47% del ox&iacute;geno te&oacute;rico requerido en   una combusti&oacute;n total) en cada uno de los niveles de temperatura operados y se   estableci&oacute; que al utilizar un 40% de agente gasificante, se obtienen en   promedio los mejores resultados en las composiciones del CO y H<sub>4</sub>,   siendo estos los gases de inter&eacute;s en el proceso de gasificaci&oacute;n.</p>     <p><i><b>Palabras   Clave:</b> crudo San   Fernando, gasificaci&oacute;n, asfaltenos, syngas.</i></p> <hr>     <p><b>RESUMEN</b></p>     <p>Neste trabalho desenvolveuse o   primeiro estudo no pa&iacute;s da obten&ccedil;&atilde;o e avalia&ccedil;&atilde;o das composi&ccedil;&otilde;es do syngas a   partir da gaseifica&ccedil;&atilde;o de asfaltenos provenientes da aplica&ccedil;&atilde;o do processo de   Desasfaltado ao cru S&atilde;o Fernando, com o objeto de avaliar op&ccedil;&otilde;es tecnol&oacute;gicas   para a sua utiliza&ccedil;&atilde;o. Para tal realizou-se o desenho e posta em marcha de um   sistema de gaseifica&ccedil;&atilde;o de asfaltenos a escala de laborat&oacute;rio, onde se empregou   uma metodologia experimental, realizando nove provas e tomando como variáveis   independentes a temperatura e o agente gaseificante (oxig&ecirc;nio). O syngas obtido   da gaseifica&ccedil;&atilde;o foi analisado por duas t&eacute;cnicas de cromatografia, as quais   reportaram a presen&ccedil;a de gases de refinaria e enxofrados. Destes resultados   experimentais evidenciase uma tend&ecirc;ncia de crescimento na composi&ccedil;&atilde;o do CO, H<sub>2</sub>&nbsp;   e enxofrados, e uma diminui&ccedil;&atilde;o na composi&ccedil;&atilde;o do CH<sub>4</sub>&nbsp;e CO<sub>2</sub>&nbsp;   com a temperatura. Avaliouse a composi&ccedil;&atilde;o do syngas com a varia&ccedil;&atilde;o do agente   gaseificante&nbsp; (33%, 40% e 47% do oxig&ecirc;nio te&oacute;rico requerido em uma   combust&atilde;o total) em cada um dos n&iacute;veis de temperatura operados e estabeleceuse   que ao utilizar um 40% de agente gaseificante, obt&eacute;m-se em m&eacute;dia os melhores   resultados nas composi&ccedil;&otilde;es do CO e H<sub>4</sub>, sendo estes os gases de   interesse no processo de gaseifica&ccedil;&atilde;o.</p>     <p><i><b>Palavras   Chave</b>: cru S&atilde;o   Fernando, gaseifica&ccedil;&atilde;o, asfaltenos, syngas.</i></p> <hr>     <p><b>INTRODUCTION</b></p>     <p>The decrease of conventional   crude oil reserves in Colombia has brought about an incremental use of heavy   crude oil reserves (Rubiales, Castilla &amp; San Fernando). Due to their high   viscosity, sulfur and metal content, these crude oils represent a challenge for   their transportation and refining. Therefore, several technological   alternatives are evaluated to utilize them in a very efficient manner. The   deasphalting process is one of these alternatives to separate the light and the   heavy fractions of crude oil, resulting in improved crude oil with less viscosity,   sulfur and metal content as well as a byproduct called asphaltenes (Wallace,   Jonson &amp; Thacker, 2001). These asphaltenes have different utilization   schemes, being one of them their submission to gasification processes.</p>     ]]></body>
<body><![CDATA[<p>Asphaltenes have a molecular   weight between 1000 and 2000, their molecule size ranges between 60-90   Armstrong and, in general terms, exhibit a boiling point greater than 540&deg;C   (Centeno, Trejo &amp; Ancheyta, 2004; Delgado, 2006). Different studies   conclude that asphaltenes are composed of condensed aromatic cores with   naphthenic and alkyl substitutions, heteroatoms and metallic compounds that can   be dispersed throughout the molecule (Navarro, 2004; Delgado, 2006).</p>     <p>The gasification process has   been a topic of research for many years (Liu &amp; Kojima, 2004); its   development and commercialization have also been a subject of analysis (Dyk,   Keyser &amp; Coertzen, 2006). Today, there are nearly 150 commercial   gasification plants in development, construction or operation (Peabody Energy,   2009). However, asphaltenes gasification has not been formally researched, a   fact that&nbsp; justifies the undertaking of this study.</p>     <p>The research objective is to   complete a design for asphaltenes gasification and the collection and   evaluation of the resulting syngas by chromatographic analyses. Based on syngas   composition and on the residues generated in the process, syngas mass yield   was determined for each trial, thus obtaining yields between 62% and 77%. </p>     <p><b>THEORETICAL FRAMEWORK</b></p>     <p>The gasification process   consists in submitting feedstocks to high temperatures (800&deg;C -1.800&deg;C) and   pressure (Huang, Fang, Chen &amp; Wang, 2003; Higman &amp; Burgt, 2007; Texaco,   1995) with a gasification agent, usually, water vapor, oxygen, air or a mixture   of them. The syngas heating value varies according to these components. This   feedstock is converted in crude gas (CO<sub>2</sub>, CH<sub>4</sub>, H<sub>2</sub>,   CO among others) that is cooled and purified to obtain a mixture of CO and H<sub>2</sub>&nbsp;(Leibold,&nbsp;   Hornung &amp; Seifert, 2008; Higman &amp; Burgt, 2007; Steynberg &amp; Dry,   2004; Texaco, 1995). Reaction rates in this range of temperature are   sufficiently high to be described by the thermodynamic equilibrium modeling of   the main gas components and coal, giving results closer to reality. This is   the foundation for the design of commercial reactors (Higman &amp; Burgt,   2007).</p>     <p>The asphaltenes gasification   process in this paper and in publications from Texaco (Wallace, Jonson &amp;   Thacker, 2001), Shell and other companies, is similar to different gasification   processes for coal, petroleum residues and biomass (Higman &amp; Burgt, 2007).   The asphaltenes gasification process, as other petroleum residues, requires   temperatures above 1000&deg;C to obtain the best results (Wallace, Jonson &amp;   Thacker, 2001; Wallace, Anderson, Rodarte &amp; Preston, 1998; Deschamps, Dezael   &amp; Franckowiak, 1986). </p>     <p>The composition of syngas   resulting from asphaltenes gasification has not been reported extensively in   any publication. Asphaltenes gasification studies result from deasphalting   processes. Therefore, petroleum companies have proposed the integration of   deasphalting processes with asphaltenes gasification (Wallace, Jonson &amp;   Thacker, 2001; Wallace, Anderson, Rodarte &amp; Preston,1998), thus creating   very attractive alternatives for crude improvement and for the application of   the byproducts resulting from the deasphalting process (asphaltene).&nbsp;   Asphaltene, in turn, is a low-cost raw material that can be submitted to a   gasification process in order to increase the profitability of these processes   (Wallace, Anderson, Rodarte &amp; Preston,1998). </p>     <p>The main reactions taking place   in gasification are: (Marano, 2003; Higman &amp; Burgt, 2007; Ouyang, Guo,   Duan, Song &amp; Yu, 2005): </p>     <p><b>Exothermal Reactions</b></p>     <p>Partial Combustion&nbsp; </p>     ]]></body>
<body><![CDATA[<p align="center"><img src="img/revistas/ctyf/v3n5/v3n5a12i1.jpg"><a name="equ1"></a></p>     <p>Total Combustion</p>     <p align="center"><img src="img/revistas/ctyf/v3n5/v3n5a12i2.jpg"><a name="equ2"></a></p>     <p>Water shift</p>     <p align="center"><img src="img/revistas/ctyf/v3n5/v3n5a12i3.jpg"><a name="equ3"></a></p>     <p>Methanation Reaction</p>     <p align="center"><img src="img/revistas/ctyf/v3n5/v3n5a12i4.jpg"><a name="equ4"></a></p>     <p><b>Endothermal Reactions</b></p>     <p>Boudouard Reaction</p>     <p align="center"><img src="img/revistas/ctyf/v3n5/v3n5a12i5.jpg"><a name="equ5"></a></p>     ]]></body>
<body><![CDATA[<p>Water-gas Reaction </p>     <p align="center"><img src="img/revistas/ctyf/v3n5/v3n5a12i6.jpg"><a name="equ6"></a></p>     <p><i><a href="#equ3">Equations 3</a> </i>through <i><a href="#equ6">6</a></i> are reversible. Their   equilibrium can be described with the Van&rsquo;t Hoff Equation that considers   the temperature effect over the equilibrium constant and, therefore, over the   equilibrium conversion. (Smith, 1991; Smith, Van Ness &amp; Abbott, 1997). </p>     <p>Van&rsquo;t Hoff Equation (Smith,   1991).</p>     <p align="center"><img src="img/revistas/ctyf/v3n5/v3n5a12i7.jpg"><a name="equ7"></a></p>     <p>The gasification process is a   controlled combustion with a reduced O<sub>2 </sub>atmosphere, using from one   third to one fifth of the O<sub>2</sub>&nbsp;required in total combustion   (Steynberg &amp; Dry, 2004). Most of the O<sub>2</sub>&nbsp;supplied in the   gasifier is consumed in the combustion reactions. The water shift reaction is   used in the adjustment of the H<sub>2</sub>/CO ratio. The objective is to   maximize the CO and H<sub>2</sub>&nbsp;content (Furimsky, 1999; Ouyang <i>et     al.</i>, 2005; Sharma, Takanohashi,&nbsp; Morishita,&nbsp; Takarada&nbsp; &amp;   Saito, 2008; Texaco, 1995). The CH<sub>4</sub>&nbsp;can be formed at low   gasification temperatures and can be reformed to increase the CO and H<sub>2</sub>&nbsp;in   the syngas from the reforming reaction <i>(</i><i><a href="#equ8">Equation 8</a></i><i>)</i> (Marano, 2003; Higman, &amp; Burgt, 2007).</p>     <p>Reforming reaction</p>     <p align="center"><img src="img/revistas/ctyf/v3n5/v3n5a12i8.jpg"><a name="equ8"></a></p>     <p>Sulfur in the feedstock is   mainly converted to small quantities of H<sub>2</sub>S and COS. Most of   nitrogen is converted into N<sub>2</sub>, with small amounts of HCN and&nbsp;   NH<sub>3</sub>&nbsp;(Secades, 2003; Hoffman, 2003; Higman &amp; Burgt, 2007;   Leibold <i>et al.</i>, 2008; Texaco, 1995).</p>     <p>Using deductions of the   thermodynamic model, Higman and Burgt (2007) determined the change in gas   composition at different pressure values (from 10 bar to 100 bar), keeping a   constant temperature of 1000&deg;C. The results of such study indicate that CH<sub>4</sub>&nbsp;and   CO<sub>2</sub>&nbsp;composition in syngas increased with pressure, while CO and   H<sub>2</sub>&nbsp;production decreased.</p>     ]]></body>
<body><![CDATA[<p>Higman and Burgt (2007)   repeated the calculation keeping a constant temperature of 1500&deg;C. They   observed the same trend as pressure increases, although their conclusion   indicates that syngas changes at this temperature are negligible. </p>     <p>In order to determine syngas   variation with temperature, (from 1000&deg;C to 1500&deg;C), Higman and&nbsp; Burgt   (2007) kept the pressure constant at 30 bar. They observed that, as temperature   increases, H<sub>2</sub>&nbsp;and CO content also increases and the content of   CO<sub>2</sub>, CH<sub>4</sub>&nbsp;and H<sub>2</sub>O decreases. This   conclusion was validated in the asphaltenes gasification.</p>     <p>Figure 1 illustrates the   available gasification technologies, together with their operation conditions   (Dyk <i>et al.,</i> 2006; Secades, 2003; Higman &amp; Burgt, 2007; Steynberg   &amp; Dry, 2004).</p>     <p align="center"><img src="img/revistas/ctyf/v3n5/v3n5a12i9.jpg"><a name="fig1"></a></p>     <p>Most of the operating plants   were constructed for the production of chemical compounds and synthetic fuel   through the Fischer-Tropsch synthesis and the clean production of electric   energy (Integrated Gasification Combined Cycle - IGCC) (Marano, 2003; Huang, <i>et     al.,</i> 2003; Leibold <i>et al.,</i> 2008; Steynberg &amp; Dry, 2004).</p>     <p><b>EXPERIMENTAL DEVELOPMENT</b></p>     <p>A laboratory-scale asphaltenes   gasification system was designed and implemented, consisting basically in a   tubular oven (<a href="#fig2">Figure 2</a>). A temperature sensor was located in   the electric oven, where the tubular reactor sits. This oven can operate at a   maximum of 1500&deg;C and the main characteristics of the reactor are: 304 SS stainless   steel drum, with a 6,35 cm external diameter and schedule 40. </p>     <p>Three basic raw materials were   used in the trials: asphaltenes, 99,99% pure oxygen and 99,99% pure argon. The   asphaltenes used comes from the San Fernando crude deasphalting process which   is classified as an extra-heavy crude oil (8,7 &deg;API). The process was conducted   by Instituto Colombiano del Petr&oacute;leo (ICP) -Ecopetrol S.A. and the main   asphaltenes characteristics are listed in <a href="#tb1">Table 1</a>.</p>     <p>The process variables   considered were determined based on the BIS BS 4445 regulation and deductions   a-ccording to Higman and Burgt (2007). The most influential variables in the   process were temperature and amount of gasification agent. A 3<sup>2</sup> factor design was used (<a href="#tb2">Table 2</a>).</p>      <p align="center"><img src="img/revistas/ctyf/v3n5/v3n5a12i10.jpg"><a name="fig1"></a></p>     ]]></body>
<body><![CDATA[<p align="center"><img src="img/revistas/ctyf/v3n5/v3n5a12i11.jpg"><a name="tb1"></a></p>     <p align="center"><img src="img/revistas/ctyf/v3n5/v3n5a12i12.jpg"><a name="tb2"></a></p>      <p><b>Methodology developed for   each trial </b></p>     <p>An asphaltenes sample weighing 15g   was placed inside the tubular reactor. The inert atmosphere was attained by   injecting Argon into the system at a volumetric flow velocity of 500 cm&sup3;/min.   Then, the reactor input and output valves were closed. Once the system was   ready (<a href="#fig3">Figure 3</a>), the heating ramps were programmed.   When the sensor reported a temperature of 600&deg;C, the input valve was opened to   let the gasification agent (oxygen) enter (<a href="#tb2">Table 2</a>) at 170 psi. The gasification agent was   allowed to react with the asphaltenes to the set point temperature (<a href="#tb3">Table 3</a>).   This process was conducted in a discontinuous system and the Syngas collection   conformed to the Regulation GPA 2166. Once the syngas was collected,   chromatographic analysis were conducted at the ICP - ECOPETROL S.A   Chromatography Laboratory for the identification of sulfur materials and   refinery gas, following the ASTM 5504 Regulation and the UPO 539 Regulation   respectively.</p>     <p>The residues left by   asphaltenes gasification were collected one day after the trial was done, since   it became necessary to wait for the cooling of the reactor.</p>        <p align="center"><img src="img/revistas/ctyf/v3n5/v3n5a12i13.jpg"><a name="fig3"></a></p>     <p align="center"><img src="img/revistas/ctyf/v3n5/v3n5a12i14.jpg"><a name="tb3"></a></p>      <p><b>RESULTS</b></p>     <p>The results obtained in the   asphaltenes gasification trials are shown in <a href="img/revistas/ctyf/v3n5/v3n5a12i15a.jpg" target="_blank">Tables 4</a>-<a href="img/revistas/ctyf/v3n5/v3n5a12i17a.jpg" target="_blank">6</a>.</p>        <p align="center"><img src="img/revistas/ctyf/v3n5/v3n5a12i15.jpg"><a name="tb4"></a></p>     ]]></body>
<body><![CDATA[<p align="center"><img src="img/revistas/ctyf/v3n5/v3n5a12i16.jpg"><a name="tb5"></a></p>      <p>Residues from trials 1 and 7   were analyzed at the Heavy Crude Oil and Spectroscopy Laboratories of   (ICP)-Ecopetrol S.A in order to determine their elementary composition. </p>     <p>These trials were selected   since they correspond to the highest and lowest levels of temperature with 40%   of gasification agent, that is, the best results were reported in these trials. </p>     <p align="center"><img src="img/revistas/ctyf/v3n5/v3n5a12i17.jpg"><a name="tb6"></a></p>     <p><b>RESULT ANALYSIS</b></p>     <p>Carbon conversion was   determined for Trials 1 and 7 (<a href="img/revistas/ctyf/v3n5/v3n5a12i15a.jpg" target="_blank">Tables 4</a> and <a href="img/revistas/ctyf/v3n5/v3n5a12i16a.jpg" target="_blank">5</a>).</p>     <p align="center"><img src="img/revistas/ctyf/v3n5/v3n5a12i18.jpg"><a name="tb7"></a></p>     <p>As explained below, increasing   temperature during asphaltenes gasification makes this process more efficient,   since it decreases the amount of tar and gasification byproducts; therefore   improving syngas composition and carbon conversion. Trial 7 showed higher   carbon conversions than trial 1 due to the fact that the residue in trial 7 was   3,66 g while trial 1 was 6 g. (<a href="img/revistas/ctyf/v3n5/v3n5a12i15a.jpg" target="_blank">Tables 4</a>, <a href="img/revistas/ctyf/v3n5/v3n5a12i17a.jpg" target="_blank">6</a>, and <a href="#tb7">7</a>). </p>     <p>The greatest mass yield of   syngas was observed in trials 7 and 9 with 77% each. The lowest mass yield was 62% in Trial 1 (<a href="img/revistas/ctyf/v3n5/v3n5a12i19a.jpg" target="_blank">Table 8</a>). </p>     <p align="center"><img src="img/revistas/ctyf/v3n5/v3n5a12i19.jpg"><a name="tb8"></a></p>     ]]></body>
<body><![CDATA[<p>The increasing tendency of CO   and H<sub>2</sub>&nbsp;proportion remained in each temperature level (<a href="#fig4">Figure 4</a>).   Variations in syngas composition with temperature show that CH<sub>2</sub>&nbsp;proportion   is significant (<a href="img/revistas/ctyf/v3n5/v3n5a12i15a.jpg" target="_blank">Table 4</a>). However, as temperature increases, CH<sub>4</sub>&nbsp;and   CO<sub>2</sub>&nbsp;proportion decreases. CO and H<sub>2</sub>&nbsp;compositions   show increments greater than 57% from the lowest to the highest level of   temperature (<a href="#fig5">Figure 5</a>).&nbsp; </p>     <p align="center"><img src="img/revistas/ctyf/v3n5/v3n5a12i20.jpg"><a name="fig4"></a></p>     <p align="center"><img src="img/revistas/ctyf/v3n5/v3n5a12i21.jpg"><a name="fig5"></a></p>     <p>It can be concluded that these   changes are the result of the effect of temperature on equilibrium conversion (<i><a href="#equ7">Equation 7</a></i>), since it was also noted that the equilibrium constant decreased   with the increment of temperature in <i><a href="#equ4">Equation 4</a></i> (Methanation reaction). On the other   hand, in <i><a href="#equ5">Equations 5</a></i> and <i><a href="#equ6">6</a></i> (Boudouard and water gas Reactions), an   increase of temperature helped the equilibrium constant and, therefore, the   equilibrium conversion. </p>     <p>The highest H<sub>2</sub>&nbsp;content   at temperatures of 900&deg;C and 950&deg;C is attained with 40% of gasification agent,   while at 1000&deg;C the highest content is attained with 33% of gasification agent.   Regarding CO, at gasification temperatures of 900&deg;C and 950&deg;C, the highest   content is attained with 40% of gasification agent, while at 1000&deg;C, the   highest CO content resulted with 47% of gasification agent (<a href="#fig6">Figure 6</a>).</p>     <p align="center"><img src="img/revistas/ctyf/v3n5/v3n5a12i22.jpg"><a name="fig6"></a></p>     <p>It is considered that these   changes are generated due to the fact that as temperature increases; the   combustion process improves, thus changing the reaction equilibrium. </p>     <p>The greatest H<sub>2</sub>/CO   ratio for the two highest temperatures is obtained with 33% of gasifying agent   (<a href="img/revistas/ctyf/v3n5/v3n5a12i15a.jpg" target="_blank">Table 4</a>).</p>     <p>The content of sulfur compounds   increases as temperature increases due to the breakdown of the asphaltenes   heaviest chains which showed the content of sulfur compounds in the feedstock (<a href="#tb1">Table 1</a>).   Therefore, the more material is gasified, the less gasification residues are   obtained (<a href="img/revistas/ctyf/v3n5/v3n5a12i16a.jpg" target="_blank">Table 5</a>) as temperature increases. </p>     <p>The oxygen composition indicates   that the heaviest asphaltenes chains did not breakdown completely during the   gasification process. Some of them were converted in coke while some of the   oxygen supplied remained without reacting. The oxygen reaction increased as   temperature increased, due to the fact that&nbsp; more material was gasified (<a href="img/revistas/ctyf/v3n5/v3n5a12i15a.jpg" target="_blank">Table 4</a>).&nbsp; </p>     ]]></body>
<body><![CDATA[<p>The presence of tars in the   process decreased with temperature, being nil at 1000&deg;C. The amount of   residues, byproducts of the gasification process, decreases as temperature   increases, since the higher the temperature, the more material is gasified. The   analysis of residues showed that a portion of them did not contain ash nor   carbon and hydrogen (<a href="img/revistas/ctyf/v3n5/v3n5a12i17a.jpg" target="_blank">Table 6</a>). This indicates that asphaltenes   require higher temperatures to reach complete gasification. </p>     <p>Comparing the results of syngas   to the results of Sasol-supplied syngas (<a href="#tb9">Table 9</a>), the&nbsp; H<sub>2</sub>&nbsp;and CO   compositions are similar to the ones obtained in trials at 1000&deg;C, while CO<sub>2 </sub>and CH<sub>4</sub>&nbsp;amounts greatly vary.&nbsp;&nbsp; </p>     <p>In order to obtain better   results in&nbsp; asphaltenes gasification, the use of a mixture of oxygen and   water vapor as gasification agent can be implemented, keeping the heat balance   of combustion and gasification reactions in the gasifiers, as the gasification   agents do (Shell, Texaco, Sasol) (Furimsky, 1999; Marano, 2003; Higman &amp;   Burgt, 2007).</p>     <p align="center"><img src="img/revistas/ctyf/v3n5/v3n5a12i23.jpg"><a name="tb9"></a></p>     <p><b>CONCLUSIONS</b></p> <ul>     <li>Results from the   asphaltenes gasification process indicate that the greater the temperature, the   higher the proportion of&nbsp; H<sub>2</sub>&nbsp;and CO and the lower the   content of tars and residues. Syngas mass yields reach 77% since there is a   greater breakdown of asphaltenes chains, thus improving the gasification   process. </li>     <li>The molar percentage of   CO showed a tendency to growth with the increment of the gasification agent at   1000&deg;C, while H<sub>2</sub>&nbsp;showed greater molar percentage when 33% and   47% of gasification agent was used at 1000&deg;C. Based on the H<sub>2</sub>&nbsp;and   CO increase, with the increment of temperature and gasification agent, the best   results were obtained when 40% of gasification agent was used. </li>     <li>The methane composition   obtained in the trials was very high if compared to the compositions reported   by some gasification plants; although as temperature increased, their   proportion decreased from 54% at 900&deg;C to 38% at 1000&deg;C. This proportion is due   to the fact that the methanation reaction is exothermal. The amount of CH<sub>4</sub>&nbsp;   can be decreased by using a mixture of oxygen and water vapor as gasification   agent, in order to increase the CO and H<sub>2</sub>&nbsp;amount present in the   syngas.</li>     <li>In order to obtain a carbon   conversion higher than 75%, the operation temperature must be above 1000&deg;C.   Therefore, it is convenient that new stu-dies consider an operation temperature   range from 1200&deg;C to 1500&deg;C.</li>     <li>The reported results   for H<sub>2&nbsp; </sub>and CO are close to the ones accounted by Sasol.   Therefore, the feasibility analysis study for the asphaltene gasification   process is considered satisfactory. It is worth mentioning that improvements   can be obtained in the results by increasing the operation temperature and   using a moderator. </li>     ]]></body>
<body><![CDATA[</ul>     <p><b>ACKNOWLEDGMENTS</b></p>     <p>The authors express their   gratitude to the Colombian Petroleum Institute (Instituto Colombiano del   Petr&oacute;leo - ICP) -Ecopetrol S.A and Universidad Industrial de Santander, for all   the support provided for the development of this research. Furthermore, the   authors acknowledge the cooperation given by engineers Jaqueline Saavedra   Rueda, Rigoberto Barrero and Maribel Casta&ntilde;eda. </p>   <hr>     <p><b>REFERENCES</b></p>     <!-- ref --><p>ASTM D 1552. (2008). Standard test   method for sulfur in petroleum products (High-temperature method).&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000107&pid=S0122-5383200900010001200001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p>ASTM D 3174. (2004). 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