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      <dc:title>Alcohol decomposition on basic/acid lignin-derived submicron diameter carbon fibers</dc:title>
      <dc:creator>García-Mateos, Francisco José</dc:creator>
      <dc:creator>Rosas-Martínez, Juana María</dc:creator>
      <dc:creator>Rodríguez-Mirasol, José</dc:creator>
      <dc:creator>Cordero-Alcántara, Tomás</dc:creator>
      <dc:subject>Lignina</dc:subject>
      <dc:subject>Carbón</dc:subject>
      <dc:description>The use of lignin, the second most abundant polymer in nature, along with a simple and versatile&#xd;
technique, electrospinning, represents an advantageous and promising approach for the preparation of&#xd;
carbon fibers. In previous studies, we have demonstrated that the incorporation of H3PO4 to the initial&#xd;
lignin solution allows for shortening the carbon fibers preparation process and that the resulting carbon&#xd;
fibers present P-surface groups that are of great interest for heterogeneous catalysis.&#xd;
Different carbon fibers catalysts have been prepared by electropinning of Alcell lignin in the absence or&#xd;
presence of H3PO4 as chemical activating agent. Carbonization at different temperatures between 500&#xd;
and 1600 ºC allows for preparing carbon fibers with a high variety of porosity and chemical surface&#xd;
properties. Diverse oxygen surface groups are presented on the carbon catalysts surface. The&#xd;
isopropanol decomposition has been used as a catalytic test to study the acid or basic character of the&#xd;
prepared carbon fibers. Carbon fibers without phosphorus surface groups generate acetone as the main&#xd;
product of the isopropanol decomposition reaction, from 400 to 600 ºC, suggesting the basic character&#xd;
of these catalysts. On the contrary, phosphorus-containing carbon fibers show high acid character,&#xd;
producing selectivity to propylene of 100 % at temperatures between 250 and 350 ºC. The most acid&#xd;
carbon fiber catalyst produced a high selectivity to ethylene and dimethyl ether for the decomposition of&#xd;
ethanol and methanol, respectively. The conversion enhancement that the presence of oxygen in the gas&#xd;
phase produced for all these reactions was also studied.</dc:description>
      <dc:date>2018-07-12T10:48:05Z</dc:date>
      <dc:date>2018-07-12T10:48:05Z</dc:date>
      <dc:date>2018</dc:date>
      <dc:date>2018-07-12</dc:date>
      <dc:type>conference output</dc:type>
      <dc:identifier>https://hdl.handle.net/10630/16214</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:relation>The world Conference on Carbon 2018</dc:relation>
      <dc:relation>Madrid, España</dc:relation>
      <dc:relation>1-5 de Julio de 2018</dc:relation>
      <dc:rights>open access</dc:rights>
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