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    H2-assisted CO2 thermochemical reduction on La0.9Ca0.1FeO3-δ membranes: a kinetics study

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    Type
    Article
    Authors
    Wu, Xiao-Yu
    Ghoniem, Ahmed F.
    Date
    2018-01-04
    Online Publication Date
    2018-01-04
    Print Publication Date
    2018-01-23
    Permanent link to this record
    http://hdl.handle.net/10754/626704
    
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    Abstract
    Kinetics data for CO2 thermochemical reduction in an isothermal membrane reactor is required to identify the rate-limiting steps. Here, we report a detailed reaction kinetics study on this process supported by an La0.9Ca0.1FeO3-δ (LCF-91) membrane. The dependence of CO2 reduction rate on various operating conditions is examined such as CO2 concentration on the feed side, fuel concentrations on the sweep side and temperatures. CO2 reduction rate is proportional to the oxygen flux across the membrane, and the measured maximum fluxes are 0.191 and 0.164 μmol cm-2 s-1 with 9.5% H2 and 11.6% CO on the sweep side at 990oC, respectively. Fuel is used to maintain the chemical potential gradient across the membrane and CO is used by construction to derive the surface reaction kinetics. This membrane also exhibits stable performances for 106 hours. A resistance-network model is developed to describe the oxygen transport process and the kinetics data are parameterized using the experimental values. The model shows a transition of the rate limiting step between the surface reactions on the feed side and the sweep side depending on the operating conditions.
    Citation
    Wu X-Y, Ghoniem AF (2017) H2-assisted CO2 thermochemical reduction on La0.9Ca0.1FeO3-δ membranes: a kinetics study. ChemSusChem. Available: http://dx.doi.org/10.1002/cssc.201701372.
    Sponsors
    The authors would like to thank both Shell and the King Abdullah University of Science and Technology (KAUST) for funding the research.
    Publisher
    Wiley
    Journal
    ChemSusChem
    DOI
    10.1002/cssc.201701372
    ae974a485f413a2113503eed53cd6c53
    10.1002/cssc.201701372
    Scopus Count
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