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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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URI: http://purl.tuc.gr/dl/dias/7F721BEC-5CFA-458B-AA31-A9EBA9ED1D3F
Έτος 2023
Τύπος Δημοσίευση σε Περιοδικό με Κριτές
Άδεια Χρήσης
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Βιβλιογραφική Αναφορά T. 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. https://doi.org/10.3390/catal13030504
Εμφανίζεται στις Συλλογές

Περίληψη

The 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.

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