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Details

Autor(en) / Beteiligte
Titel
Proton conductivity in yttrium-doped barium cerate under nominally dry reducing conditions for application in chemical synthesis
Ist Teil von
  • Journal of materials chemistry. A, Materials for energy and sustainability, 2019, Vol.7 (3), p.18135-18142
Ort / Verlag
Cambridge: Royal Society of Chemistry
Erscheinungsjahr
2019
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • Electrochemical membrane reactors using proton-conducting ceramics are promising and efficient technologies for the production of valuable chemical products by the promotion of hydrogenation/dehydrogenation reactions. Due to a very high equilibrium constant for hydration, yttrium-doped barium cerate, BaCe 0.9 Y 0.1 O 3− δ (BCY10), presents one of the highest proton conductivities at low temperatures among known proton-conducting ceramic oxides ( e.g. ∼10 −3 S cm −1 at 400 °C under humidified atmospheres, p H 2 O ∼ 10 −2 atm). Nonetheless, BCY10 is commonly discarded for such applications due to its poor chemical stability towards hydroxide or carbonate formation. Moreover, the use of humidified atmospheres may not be feasible for many chemical syntheses, due to undesired side reactions. The current work, therefore, combines impedance spectroscopy, thermogravimetric analysis, coulometric titration and defect chemistry modelling to assess the limits for pure protonic conductivity in BCY10 in nominally dry atmospheres ( p H 2 O ∼ 10 −4 to 10 −5 atm, at low temperatures <600 °C), conditions where its stability and applicability to industrially relevant chemical synthesis reactions may be maintained, whilst still being hydrated. This work, thereby, unlocks a new application area for proton-conducting ceramics in a wide range of hydrogenation/de-hydrogenation reactions in the nominal absence of water. The applicability limits of BaCe 0.9 Y 0.1 O 3− δ highlighted for use as a membrane in electrochemical reactors operating under nominally dry conditions.
Sprache
Englisch
Identifikatoren
ISSN: 2050-7488
eISSN: 2050-7496
DOI: 10.1039/c9ta04584h
Titel-ID: cdi_crossref_primary_10_1039_C9TA04584H

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