<?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>2026-04-13T05:46:03Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:2445/164941" metadataPrefix="marc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:2445/164941</identifier><datestamp>2025-12-04T21:00:33Z</datestamp><setSpec>com_2072_1057</setSpec><setSpec>col_2072_478796</setSpec><setSpec>col_2072_478917</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Coria, Gabriela</subfield>
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      <subfield code="a">Sirés Sadornil, Ignacio</subfield>
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      <subfield code="a">Brillas, Enric</subfield>
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      <subfield code="a">Nava, José L.</subfield>
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      <subfield code="c">2020-06-09T11:19:46Z</subfield>
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      <subfield code="c">2020-06-09T11:19:46Z</subfield>
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      <subfield code="a">This study focuses on the role of the anode material for the electrochemical degradation of the top-selling anti-inflammatory drug naproxen (NPX). Aqueous solutions containing 40 mg L−1 NPX sodium in 0.050 M NaClO4 at pH 3.0 were comparatively treated by electrochemical advanced oxidation processes (EAOPs) like electro-oxidation with electrogenerated H2O2 (EO-H2O2), electro-Fenton (EF) and UVA photoelectro-Fenton (PEF). The experiments were performed in a 2.5 L flow plant equipped with an annular glass photoreactor coupled to a cell with a Pt, IrO2-based (DSA-O2), RuO2-based (DSA-Cl2) or boron-doped diamond (BDD) anode and an air-diffusion cathode to electrogenerate H2O2. In EF and PEF, 0.50 mM Fe2+ was added as catalyst. At 50 mA cm-2, the oxidation power of EAOPs rose in the order: EO-H2O2 &lt; EF &lt; PEF, regardless of the anode used. The IrO2-based anode led to greater mineralization in EO-H2O2 and EF. In contrast, the BDD anode allowed an almost total mineralization in PEF, being superior to 85% attained with the other three materials. DSA, a significantly cheap anode compared to Pt and BDD, can then be a suitable candidate for treating NPX solutions by EAOPs. For each process, the mineralization current efficiency and specific energy consumption were determined. The NPX concentration decay always followed a pseudo-first-order kinetics and, in PEF, it was enhanced in the sequence: RuO2-based &lt; Pt &lt; BDD &lt; IrO2-based. GC-MS analysis of treated solutions allowed detecting six aromatic products, whereas maleic and oxalic acids were identified by ion-exclusion HPLC. A reaction sequence for the degradation of NPX by EAOPs is finally proposed.</subfield>
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      <subfield code="a">Oxidació electroquímica</subfield>
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      <subfield code="a">Agents antiinflamatoris</subfield>
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      <subfield code="a">Depuració de l'aigua</subfield>
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      <subfield code="a">Electrolytic oxidation</subfield>
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      <subfield code="a">Antiinflammatory agents</subfield>
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      <subfield code="a">Water purification</subfield>
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      <subfield code="a">Influence of the anode material on the degradation of naproxen by Fenton-based electrochemical processes</subfield>
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