Thanks to its high hydrogen permeability and good chemical stability in moist CO2 environments, BaCe0.65Zr0.20Y0.15O3-delta-Ce0.85Gd0.15O2-delta mixed conducting material is considered one of the most promising candidates for hydrogen separation ceramic membranes. In this work, its chemical stability under H2S-rich atmosphere was systematically investigated by in-situ electrochemical characterizations and ex-situ structural, chemical and morphological analyses. A performance degradation of the total conductivity depending on the H2S content was observed: at 700 degrees C and under 1500 and 700 ppm of H2S the conductivity drop was 15% and 2% respectively. The complementary information gathered by morphological and chemical analyses showed that the changes responsible for the total conductivity degradation are mainly confined to the surface of the membrane. Indeed, after the exposure to the H2S-containing atmosphere, some traces of sulfur-related compounds were detected only on the top of the membrane while the bulk preserved a fully dense structure with well-defined grain boundaries and no evidence of cracks. However, no evidence of S-based compounds were revealed by structural investigations, probably due to the detection limit of these techniques and/or to the low crystallinity of the secondary phases. Contrary to Pd-based membranes that are severely deteriorated by a few ppm of sulfur, this material shows an acceptable stability even under 700 ppm of H2S and could be attractive for tailored applications such as, for example, operations related to steam reforming of methane often containing 10-300 ppm of H2S.

Enhanced sulfur tolerance of BaCe0.65Zr0.20Y0.15O3-delta-Ce0.85Gd0.15O2-delta composite for hydrogen separation membranes

Mortalo C;Deambrosis S;Rancan M;Armelao L;Fabrizio M
2018

Abstract

Thanks to its high hydrogen permeability and good chemical stability in moist CO2 environments, BaCe0.65Zr0.20Y0.15O3-delta-Ce0.85Gd0.15O2-delta mixed conducting material is considered one of the most promising candidates for hydrogen separation ceramic membranes. In this work, its chemical stability under H2S-rich atmosphere was systematically investigated by in-situ electrochemical characterizations and ex-situ structural, chemical and morphological analyses. A performance degradation of the total conductivity depending on the H2S content was observed: at 700 degrees C and under 1500 and 700 ppm of H2S the conductivity drop was 15% and 2% respectively. The complementary information gathered by morphological and chemical analyses showed that the changes responsible for the total conductivity degradation are mainly confined to the surface of the membrane. Indeed, after the exposure to the H2S-containing atmosphere, some traces of sulfur-related compounds were detected only on the top of the membrane while the bulk preserved a fully dense structure with well-defined grain boundaries and no evidence of cracks. However, no evidence of S-based compounds were revealed by structural investigations, probably due to the detection limit of these techniques and/or to the low crystallinity of the secondary phases. Contrary to Pd-based membranes that are severely deteriorated by a few ppm of sulfur, this material shows an acceptable stability even under 700 ppm of H2S and could be attractive for tailored applications such as, for example, operations related to steam reforming of methane often containing 10-300 ppm of H2S.
2018
Istituto di Chimica della Materia Condensata e di Tecnologie per l'Energia - ICMATE
Inglese
564
123
132
10
https://www.sciencedirect.com/science/article/pii/S0376738818314728?via=ihub
Composite membrane
Hydrogen separation
Chemical stability
H2S-rich atmosphere
Highlights o Chemical stability of BCZ20Y15-GDC15 composite under H2S was investigated. o A decrease of the total conductivity depending on the H2S content was observed. o The bulk of the BCZ20Y15-GDC15 membrane conserved its integrity after H2S treatments. o A suitable stability was observed at 700 °C under 700 ppm of H2S.
9
info:eu-repo/semantics/article
262
Mortalo, C; Rebollo, E; Escolastico, S; Deambrosis, S; Haassanto, K; Rancan, M; Dittmeyer, R; Armelao, L; Fabrizio, M
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/344354
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