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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1016/j.cep.2018.03.024</dc:identifier><dc:language>eng</dc:language><dc:creator>Gangurde, L.S.</dc:creator><dc:creator>Sturm, G.S.J.</dc:creator><dc:creator>Valero-Romero, M.J.</dc:creator><dc:creator>Mallada, R.</dc:creator><dc:creator>Santamaria, J.</dc:creator><dc:creator>Stankiewicz, A.I.</dc:creator><dc:creator>Stefanidis, G.D.</dc:creator><dc:title>Synthesis, characterization, and application of ruthenium-doped SrTiO3 perovskite catalysts for microwave-assisted methane dry reforming</dc:title><dc:identifier>ART-2018-105887</dc:identifier><dc:description>A series of ruthenium-doped strontium titanate (SrTiO3) perovskite catalysts were synthesized by conventional and microwave-assisted hydrothermal methods. The structure was analyzed by X-Ray diffraction (XRD) confirming the formation of the perovskite phase with some TiO2 anatase phase in all the catalysts. Microwave irradiation decreases the temperature and time of synthesis from 220 °C for 24 h (conventional heating) to 180 °C for 1h, without affecting the formation of perovskite. A 7 wt. % ruthenium-doped SrTiO3 catalyst showed the best dielectric properties, and thus its catalytic activity was evaluated for the methane dry reforming reaction under microwave heating in a custom fixed-bed quartz reactor. Microwave power, CH4:CO2 vol. % feed ratio and gas hourly space velocity (GHSV) were varied in order to determine the best conditions for performing dry reforming with high reactants conversions and H2/CO ratio. Stable maximum CH4 and CO2 conversions of ~99.5% and ~94%, respectively, at H2/CO ~0.9 were possible to reach with the 7 wt. % ruthenium-doped SrTiO3 catalyst exposed to maximum temperatures in the vicinity of 940 °C. A comparative theoretical scale-up study shows significant improvement in H2 production capability in the case of the perovskite catalyst compared to carbon-based catalysts.</dc:description><dc:date>2018</dc:date><dc:source>http://zaguan.unizar.es/record/78712</dc:source><dc:doi>10.1016/j.cep.2018.03.024</dc:doi><dc:identifier>http://zaguan.unizar.es/record/78712</dc:identifier><dc:identifier>oai:zaguan.unizar.es:78712</dc:identifier><dc:relation>info:eu-repo/grantAgreement/EC/FP7/267348/EU/Towards Perfect Chemical Reactors:Engineering the Enhanced Control of Reaction Pathways at Molecular Level via Fundamental Concepts of Process Intensification/TOPCHEM</dc:relation><dc:identifier.citation>CHEMICAL ENGINEERING AND PROCESSING 127 (2018), 178-190</dc:identifier.citation><dc:rights>by-nc-nd</dc:rights><dc:rights>http://creativecommons.org/licenses/by-nc-nd/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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