Effect of A-site lanthanum doping on the CO2 tolerance of SrCo0.8Fe0.2O3--δ oxygen-transporting membranes

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Original languageEnglish
Pages (from-to)122-130
Number of pages9
JournalJournal of membrane science
Volume437
Early online date5 Mar 2013
Publication statusPublished - 15 Jun 2013

Abstract

The SrCo0.8Fe0.2O3-δ (SCF) perovskite was systematically doped with increasing lanthanum content up to 60wt% on the A-site to investigate the effect on CO2 tolerance. Different powders were prepared by a sol-gel method and the materials were characterized by in-situ X-ray diffraction (XRD) and long-term oxygen permeation measurements in CO2-containing atmospheres. The microstructure was investigated using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). All powders exhibit cubic perovskite structure except the rhombohedral La0.6Sr0.4Co0.8Fe0.2O3-δ (LSCF 6482), which however, shows a phase transition into cubic perovskite structure at higher temperature. By doping 20wt% lanthanum, the tolerance against CO2 is considerably increased and doping with 60wt% lanthanum resulted in a stable oxygen permeation performance in CO2 atmosphere for at least 200h. Oxygen permeation experiments in an air/helium gradient showed that with increasing lanthanum content the oxygen permeation flux decreases. Microstructure analysis of the membranes after CO2 operation showed that the carbonate preferentially forms a dense layer at the carbon dioxide exposed sweep side of the membranes.

Keywords

    Carbon dioxide, In-situ X-ray diffraction, Long-term oxygen permeation, Oxygen-transporting membrane, Transmission electron microscopy

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Effect of A-site lanthanum doping on the CO2 tolerance of SrCo0.8Fe0.2O3--δ oxygen-transporting membranes. / Klande, Tobias; Ravkina, Olga; Feldhoff, Armin.
In: Journal of membrane science, Vol. 437, 15.06.2013, p. 122-130.

Research output: Contribution to journalArticleResearchpeer review

Klande T, Ravkina O, Feldhoff A. Effect of A-site lanthanum doping on the CO2 tolerance of SrCo0.8Fe0.2O3--δ oxygen-transporting membranes. Journal of membrane science. 2013 Jun 15;437:122-130. Epub 2013 Mar 5. doi: 10.1016/j.memsci.2013.02.051
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abstract = "The SrCo0.8Fe0.2O3-δ (SCF) perovskite was systematically doped with increasing lanthanum content up to 60wt% on the A-site to investigate the effect on CO2 tolerance. Different powders were prepared by a sol-gel method and the materials were characterized by in-situ X-ray diffraction (XRD) and long-term oxygen permeation measurements in CO2-containing atmospheres. The microstructure was investigated using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). All powders exhibit cubic perovskite structure except the rhombohedral La0.6Sr0.4Co0.8Fe0.2O3-δ (LSCF 6482), which however, shows a phase transition into cubic perovskite structure at higher temperature. By doping 20wt% lanthanum, the tolerance against CO2 is considerably increased and doping with 60wt% lanthanum resulted in a stable oxygen permeation performance in CO2 atmosphere for at least 200h. Oxygen permeation experiments in an air/helium gradient showed that with increasing lanthanum content the oxygen permeation flux decreases. Microstructure analysis of the membranes after CO2 operation showed that the carbonate preferentially forms a dense layer at the carbon dioxide exposed sweep side of the membranes.",
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T1 - Effect of A-site lanthanum doping on the CO2 tolerance of SrCo0.8Fe0.2O3--δ oxygen-transporting membranes

AU - Klande, Tobias

AU - Ravkina, Olga

AU - Feldhoff, Armin

N1 - Funding Information: The authors greatly acknowledge financial support from the Chinese-German Centre for Science ( GZ676 ) and the Deutsche Forschungsgemeinschaft ( FE 928/4-1 ) and fruitful discussions with Prof. Jürgen Caro.

PY - 2013/6/15

Y1 - 2013/6/15

N2 - The SrCo0.8Fe0.2O3-δ (SCF) perovskite was systematically doped with increasing lanthanum content up to 60wt% on the A-site to investigate the effect on CO2 tolerance. Different powders were prepared by a sol-gel method and the materials were characterized by in-situ X-ray diffraction (XRD) and long-term oxygen permeation measurements in CO2-containing atmospheres. The microstructure was investigated using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). All powders exhibit cubic perovskite structure except the rhombohedral La0.6Sr0.4Co0.8Fe0.2O3-δ (LSCF 6482), which however, shows a phase transition into cubic perovskite structure at higher temperature. By doping 20wt% lanthanum, the tolerance against CO2 is considerably increased and doping with 60wt% lanthanum resulted in a stable oxygen permeation performance in CO2 atmosphere for at least 200h. Oxygen permeation experiments in an air/helium gradient showed that with increasing lanthanum content the oxygen permeation flux decreases. Microstructure analysis of the membranes after CO2 operation showed that the carbonate preferentially forms a dense layer at the carbon dioxide exposed sweep side of the membranes.

AB - The SrCo0.8Fe0.2O3-δ (SCF) perovskite was systematically doped with increasing lanthanum content up to 60wt% on the A-site to investigate the effect on CO2 tolerance. Different powders were prepared by a sol-gel method and the materials were characterized by in-situ X-ray diffraction (XRD) and long-term oxygen permeation measurements in CO2-containing atmospheres. The microstructure was investigated using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). All powders exhibit cubic perovskite structure except the rhombohedral La0.6Sr0.4Co0.8Fe0.2O3-δ (LSCF 6482), which however, shows a phase transition into cubic perovskite structure at higher temperature. By doping 20wt% lanthanum, the tolerance against CO2 is considerably increased and doping with 60wt% lanthanum resulted in a stable oxygen permeation performance in CO2 atmosphere for at least 200h. Oxygen permeation experiments in an air/helium gradient showed that with increasing lanthanum content the oxygen permeation flux decreases. Microstructure analysis of the membranes after CO2 operation showed that the carbonate preferentially forms a dense layer at the carbon dioxide exposed sweep side of the membranes.

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KW - In-situ X-ray diffraction

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