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    <subfield code="a">10.1016/j.cej.2024.151962</subfield>
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    <subfield code="2">sideral</subfield>
    <subfield code="a">138644</subfield>
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    <subfield code="a">ART-2024-138644</subfield>
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    <subfield code="a">eng</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Tsiotsias, Anastasios I.</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Integrating capture and methanation of CO2 using physical mixtures of Na-Al2O3 and mono-/ bimetallic (Ru)Ni/Pr-CeO2</subfield>
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    <subfield code="c">2024</subfield>
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    <subfield code="a">The integrated capture and methanation of CO2 is hereby realized via the use of physical mixtures of a 12 % Na2O/Al2O3 adsorbent and either a monometallic (10 % Ni/Pr-CeO2) or a bimetallic (1 % Ru, 10 % Ni/Pr–CeO2) catalyst. The effect of the weight ratio between the catalyst and the adsorbent components is studied and it is found to exert a great influence in the reaction kinetics and the CH4 production capacity, with the 1:3 catalyst: adsorbent weight ratio (2.5 wt% Ni for both physically mixed materials and 0.25 wt% Ru for the bimetallic material) providing the highest CH4 yield. It is further shown that the materials offer high activity, stability and CH4 selectivity at just 300 °C, even under the co–presence of O2 and H2O during CO2 adsorption, a fact attributable to the preservation of the Ni-CeO2 contact, which is known to afford a high reducibility to the catalytically active Ni phase. The presence of Ru can further enhance the material reducibility and activity under low operation temperatures and catalyst: adsorbent weight ratios, while also mitigating the negative effect of the O2 and H2O presence in the adsorption feed. A CH4 yield of 0.24 mmol/g after 10 consecutive cycles of CO2 adsorption (under O2 and H2O containing gas) and methanation is achieved for the monometallic Ni-based physically mixed material, compared to 0.29 mmol/g in the case of the Ru–Ni bimetallic physically mixed material.</subfield>
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    <subfield code="a">All rights reserved</subfield>
    <subfield code="u">http://www.europeana.eu/rights/rr-f/</subfield>
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    <subfield code="b">3 / 83 = 0.036</subfield>
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    <subfield code="c">2024</subfield>
    <subfield code="d">Q1</subfield>
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    <subfield code="a">Industrial and Manufacturing Engineering</subfield>
    <subfield code="c">2024</subfield>
    <subfield code="d">Q1</subfield>
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    <subfield code="a">Environmental Chemistry</subfield>
    <subfield code="c">2024</subfield>
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    <subfield code="a">Chemistry (miscellaneous)</subfield>
    <subfield code="c">2024</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Charisiou, Nikolaos D.</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Hussien, Aseel G.S.</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Sebastian, Victor</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-6873-5244</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Polychronopoulou, Kyriaki</subfield>
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    <subfield code="a">Goula, Maria A.</subfield>
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    <subfield code="1">5005</subfield>
    <subfield code="2">555</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Ing.Quím.Tecnol.Med.Amb.</subfield>
    <subfield code="c">Área Ingeniería Química</subfield>
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  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">491 (2024), 151962 [18 pp.]</subfield>
    <subfield code="p">Chem. eng. j.</subfield>
    <subfield code="t">Chemical Engineering Journal</subfield>
    <subfield code="x">1385-8947</subfield>
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