<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-01T13:38:11Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/7938" metadataPrefix="marc">https://riuma.uma.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:riuma.uma.es:10630/7938</identifier><datestamp>2026-02-03T12:26:52Z</datestamp><setSpec>com_10630_2254</setSpec><setSpec>col_10630_37959</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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   <datafield ind2=" " ind1=" " tag="042">
      <subfield code="a">dc</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Valero-Romero, María José</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Rodríguez-Mirasol, José</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Cordero-Alcántara, Tomás</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="260">
      <subfield code="c">2014-07-28</subfield>
   </datafield>
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      <subfield code="a">Activated carbons materials have attracted considerable attention because of their interesting application in many fields, such as catalysis, gas and liquid phase adsorption and gas and energy&#xd;
storage. However, the use of carbon materials in catalysis is limited since they would gasify to CO2&#xd;
(or CO) in the presence of oxygen at relatively low temperatures. On the other hand, it has been&#xd;
shown that it is possible to prepare carbon materials with a relatively large amount of phosphorus&#xd;
on the carbon surface by chemical activation of lignocellulosic materials with phosphoric acid [1].&#xd;
This activation method leads, in certain operation conditions, to the generation of phosphorus&#xd;
surface complexes in form of C-O-PO3, C-PO3 and C3PO groups, which present a very high thermal&#xd;
stability and confer to the carbons certain surface properties of great interest in heterogeneous&#xd;
catalysis applications, such as high oxidation resistance and surface acidity. The main purpose of&#xd;
the present work is to study the role of the phosphorus surface groups of these activated carbons on&#xd;
the carbon surface oxidation and reduction reactions.&#xd;
An extensive study of the oxidation evolution of the activated carbon surface has been carried out&#xd;
by subjecting the carbon to thermal treatments in oxidizing and inert conditions, using different&#xd;
techniques including temperature-programmed desorption (TPD) and X-ray photoelectron&#xd;
spectroscopy (XPS) for the characterization of the obtained carbons. It has been proved that&#xd;
phosphorus surface groups preferentially trap oxygen and are transformed from less to moreoxidized&#xd;
species prior to carbon gasification, even at low temperature. These experimental results&#xd;
evidence the role of phosphorus surface groups on the inhibition of carbon oxidation and&#xd;
gasification. The high capacity of these phosphorus species to be oxidized results in activated&#xd;
carbons with a high amount of oxygen surface groups of acidic character and relatively high&#xd;
thermal stability.&#xd;
The reduction and re-oxidation of the (phosphorus) surface groups have also been proved to be&#xd;
reversible through successive thermal treatments in oxidizing and inert conditions. The new surface&#xd;
sites generated during the reduction conditions (probably of C-PO type) may react with oxygen&#xd;
from air and regenerate the C–O–PO system, indicating the presence of redox sites on the surface of&#xd;
the activated carbon. These results open new and attractive possibilities for the use of these carbon&#xd;
materials as catalytic supports or as catalysts by themselves for reactions that take place under&#xd;
oxidizing conditions and at relatively high temperatures.</subfield>
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      <subfield code="a">http://hdl.handle.net/10630/7938</subfield>
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      <subfield code="a">Carbón activado</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">Ácido fosfórico</subfield>
   </datafield>
   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">Oxidation of activated carbons containing surface phosphorus functionalities</subfield>
   </datafield>
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