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    Selectivity enhancement for higher alcohol product in Fischer-Tropsch synthesis over nickel-substituted La0.9Sr0.1CoO3 perovskite catalysts

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    Authors
    Ao, M.
    Pham, Gia
    Sage, V.
    Pareek, Vishnu
    Date
    2017
    Type
    Journal Article
    
    Metadata
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    Citation
    Ao, M. and Pham, G. and Sage, V. and Pareek, V. 2017. Selectivity enhancement for higher alcohol product in Fischer-Tropsch synthesis over nickel-substituted La0.9Sr0.1CoO3 perovskite catalysts. Fuel. 206: pp. 390-400.
    Source Title
    Fuel
    DOI
    10.1016/j.fuel.2017.06.036
    ISSN
    0016-2361
    School
    Department of Chemical Engineering
    URI
    http://hdl.handle.net/20.500.11937/55339
    Collection
    • Curtin Research Publications
    Abstract

    © 2017 Elsevier Ltd The performance of La 0.9 Sr 0.1 Co 1-x Ni x O 3 perovskite catalysts with different Ni substitution levels was evaluated in the Fischer-Tropsch (F-T) synthesis for higher alcohol production. It was found that Ni substitution improved the catalyst's reducibility and had a positive effect on higher alcohol synthesis (HAS) from syngas. Only a limited amount of Ni ions can enter into the perovskite structure and then form Co-Ni alloy after reduction. Catalyst characterisation and activity test results indicate that the synergistic effects of the two metal species in the Co-Ni are responsible for the catalytic activity improvement. For high Ni-substituted perovskite catalysts (x = 0.5), the extra-lattice Ni segregates on the catalyst surface and promotes CO methanation during the F-T reaction. A significant deviation of methanol selectivity from the Anderson-Schulz-Flory (ASF) linear distribution was detected for catalysts containing both Ni and Co, suggesting that the alcohol formation mechanism is altered with nickel substitution in La 0.9 Sr 0.1 Co 1-x Ni x O 3 perovskite catalysts. The La 0.9 Sr 0.1 Co 0.9 Ni 0.1 O 3 perovskite catalyst exhibited the highest selectivity towards higher alcohols. The effect of reaction temperature on the catalytic activity is also discussed.

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