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Transient kinetics study of catalytic char gasification in carbon dioxide

Journal Article · · Industrial and Engineering Chemistry Research; (United States)
DOI:https://doi.org/10.1021/ie00056a009· OSTI ID:7172293
;  [1]
  1. Pennsylvania State Univ., University Park, PA (United States). Dept. of Materials Science and Engineering

In this paper, the deactivation behavior of K, Ca, and Ni catalysts during carbon (char) gasification in CO{sub 2} is investigated. Correlations were sought between gasification rates and reactive surface areas (RSA) of the chars. In addition, the results allowed some speculation on recently proposed mechanisms of catalysis. An excellent correlation was found in the case of K catalysis, suggesting the rate-determining step in the overall mechanism to be the same as in the uncatalyzed reaction, i.e., desorption of the reactive C(O) intermediate. For the Ca-catalyzed reaction, the quality of the correlation depended on catalyst dispersion, suggesting that an additional process, besides the direct decomposition of the reactive C(O) intermediate, contributed to the transient evolution of CO (e.g., oxygen spillover). No correlation was found for Ni-catalyzed gasification; an oxygen-transfer mechanism is proposed to explain these findings. Mixed catalyst systems (Ca/K, K/Ni, Ca/Ni) were also studied. An excellent correlation between reactivity and RSA was observed in cases where the K-catalyzed reaction was dominant.

OSTI ID:
7172293
Journal Information:
Industrial and Engineering Chemistry Research; (United States), Journal Name: Industrial and Engineering Chemistry Research; (United States) Vol. 30:8; ISSN IECRE; ISSN 0888-5885
Country of Publication:
United States
Language:
English