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Unveiling the role of in situ sulfidation and H2O excess on H2S decomposition to carbon-free H2 over cobalt/ceria catalysts

Kraia Tzouliana, Varvoutis Georgios, Marnellos, Georges E, Konsolakis Michail

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URIhttp://purl.tuc.gr/dl/dias/7F721BEC-5CFA-458B-AA31-A9EBA9ED1D3F-
Identifierhttps://doi.org/10.3390/catal13030504-
Identifierhttps://www.mdpi.com/2073-4344/13/3/504-
Languageen-
Extent18 pagesen
TitleUnveiling the role of in situ sulfidation and H2O excess on H2S decomposition to carbon-free H2 over cobalt/ceria catalystsen
CreatorKraia Tzoulianaen
CreatorVarvoutis Georgiosen
CreatorMarnellos, Georges Een
CreatorKonsolakis Michailen
CreatorΚονσολακης Μιχαηλel
PublisherMDPIen
DescriptionThe work was performed within the frame of the joint program Black-Sea ERA.NET under the FP-7 initiative of the European Commission and funded by the Greek General Secretariat for Research and Technology GSRT (grant No. 11BS_10_28) and the project “Development of New Innovative Low Carbon Footprint Energy Technologies to Enhance Excellence in the Region of Western Macedonia” (MIS 5047197) which is implemented under the Action “Reinforcement of the Research and Innovation Infrastructure”, funded by the Operational Programme “Competitiveness, Entrepreneurship and Innovation” (NSRF 2014–2020) and co-financed by Greece and the European Union (European Regional Development Fund).en
Content SummaryThe emerging energy and environmental concerns nowadays are highlighting the need to turn to clean fuels, such as hydrogen. In this regard, hydrogen sulfide (H2S), an abundant chemical compound found in several natural sources and industrial streams, can be considered a potential carbon-free H2 source through its decomposition. In the present work, the H2S decomposition performance of Co3O4/CeO2 mixed oxide catalysts toward hydrogen production is investigated under excess H2O conditions (1 v/v% H2S, 90 v/v% H2O, Ar as diluent), simulating the concentrated H2S-H2O inflow by the Black Sea deep waters. The effect of key operational parameters such as feed composition, temperature (550–850 °C), and cobalt loading (0–100 wt.%) on the catalytic performance of Co3O4/CeO2 catalysts was systematically explored. In order to gain insight into potential structure-performance relationships, various characterization studies involving BET, XRD, SEM/EDX, and sulfur elemental analysis were performed over the fresh and spent samples. The experimental results showed that the 30 wt.% Co/CeO2 catalyst demonstrated the optimum catalytic performance over the entire temperature range with a H2 production rate of ca. 2.1 μmol H2∙g−1·s−1 at 850 °C and a stable behavior after 10 h on stream, ascribed mainly to the in-situ formation of highly active and stable cobalt sulfided phases.en
Type of ItemPeer-Reviewed Journal Publicationen
Type of ItemΔημοσίευση σε Περιοδικό με Κριτέςel
Licensehttp://creativecommons.org/licenses/by/4.0/en
Date of Item2025-05-28-
Date of Publication2023-
SubjectH2S decomposition/reformingen
SubjectH2O excess conditionsen
SubjectCarbon-free H2 productionen
SubjectCo3O4/CeO2 catalystsen
SubjectCobalt sulfide phaseen
Bibliographic CitationT. Kraia, G. Varvoutis, G. E. Marnellos, and M. Konsolakis, “Unveiling the role of in situ sulfidation and H2O excess on H2S decomposition to carbon-free H2 over cobalt/ceria catalysts,” Catalysts, vol. 13, no. 3, Feb. 2023, doi: 10.3390/catal13030504.en

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