<?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>2026-06-27T22:48:18Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/107225" metadataPrefix="mods">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/107225</identifier><datestamp>2025-03-18T12:39:58Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</setSpec></header><metadata><mods:mods xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-1.xsd">
   <mods:name>
      <mods:namePart>Martín Martínez, María</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Álvarez Torrellas, Silvia</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>García Rodríguez, Juan</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Silva, Adrián M. T. </mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Faria, Joaquim L. </mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Gomes, Helder T. </mods:namePart>
   </mods:name>
   <mods:extension>
      <mods:dateAvailable encoding="iso8601">2024-07-30T10:38:20Z</mods:dateAvailable>
   </mods:extension>
   <mods:extension>
      <mods:dateAccessioned encoding="iso8601">2024-07-30T10:38:20Z</mods:dateAccessioned>
   </mods:extension>
   <mods:originInfo>
      <mods:dateIssued encoding="iso8601">2018-09</mods:dateIssued>
   </mods:originInfo>
   <mods:identifier type="citation">Maria Martin-Martinez, Silvia Álvarez-Torrellas, Juan García, Adrián M.T. Silva, Joaquim L. Faria, Helder T. Gomes, Exploring the activity of chemical-activated carbons synthesized from peach stones as metal-free catalysts for wet peroxide oxidation, Catalysis Today, Volume 313, 2018, Pages 20-25, ISSN 0920-5861, https://doi.org/10.1016/j.cattod.2018.01.003.</mods:identifier>
   <mods:identifier type="issn">0920-5861</mods:identifier>
   <mods:identifier type="doi">10.1016/j.cattod.2018.01.003</mods:identifier>
   <mods:identifier type="uri">https://hdl.handle.net/20.500.14352/107225</mods:identifier>
   <mods:identifier type="officialurl">https://doi.org/10.1016/j.cattod.2018.01.003</mods:identifier>
   <mods:identifier type="relatedurl">https://www.sciencedirect.com/science/article/pii/S0920586118300038</mods:identifier>
   <mods:abstract>Peach stones were used as raw material for the synthesis of activated carbons with different properties. Firstly, peach stones were chemically activated using a 12M H3PO4 solution and carbonized under flowing air (400 °C). The obtained activated carbon, named as PS, is characterized by a high surface development (SBET=1262m2 g−1) and acidic character (pHPZC=4.2). A fraction of PS was further carbonized under N2 atmosphere at 800 °C to remove surface functionalities and to increase its basicity (PS-800). In addition, a Pt catalyst supported on PS (3% w/w Pt/PS) was synthesized by incipient wetness impregnation, resulting in a considerable hydrophilicity increasing. The synthesized materials were tested in the catalytic wet peroxide oxidation (CWPO) of highly concentrated solutions of 4-nitrophenol (4-NP, 5 g L−1) during 24 h experiments, conducted at relatively mild operating conditions (T=50–110 °C, pH=3, catalyst load=2.5 g L−1 and [H2O2]0=17.8 g L−1, corresponding to the stoichiometric amount of H2O2 needed for the complete mineralization of 4-NP). It was observed that the increase of electron-donating functionalities in PS-800 promotes the generation of reactive HO% radicals, being the activity towards CWPO twice higher than that obtained with the pristine PS. Besides, increasing operating temperature substantially enhances CWPO, finding a 80% of 4-NP removal at 110 °C. On the other hand, despite the sharp increment in H2O2 decomposition due to the presence of Pt particles in Pt/PS catalyst, this decomposition is inefficient in all cases, with a consequent poor pollutant removal. This can be attributed to the recombination of HO% radicals into non-reactive species −scavenging effects, promoted by the hydrophilicity of the catalyst.</mods:abstract>
   <mods:language>
      <mods:languageTerm>eng</mods:languageTerm>
   </mods:language>
   <mods:accessCondition type="useAndReproduction">http://creativecommons.org/licenses/by-nc-nd/4.0/</mods:accessCondition>
   <mods:accessCondition type="useAndReproduction">restricted access</mods:accessCondition>
   <mods:accessCondition type="useAndReproduction">Attribution-NonCommercial-NoDerivatives 4.0 International</mods:accessCondition>
   <mods:titleInfo>
      <mods:title>Exploring the activity of chemical-activated carbons synthesized from peach stones as metal-free catalysts for wet peroxide oxidation</mods:title>
   </mods:titleInfo>
   <mods:genre>journal article</mods:genre>
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