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Reduction Kinetics of Perovskite Oxides for Selective Hydrogen Combustion in the Context of Olefin Production
Author(s) -
Dudek Ryan B.,
Tian Yuan,
Jin Gaochen,
Blivin Millicent,
Li Fanxing
Publication year - 2020
Publication title -
energy technology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.91
H-Index - 44
eISSN - 2194-4296
pISSN - 2194-4288
DOI - 10.1002/ente.201900738
Subject(s) - context (archaeology) , catalysis , redox , dehydrogenation , chemistry , selectivity , olefin fiber , hydrogen , ethylene , chemical looping combustion , kinetics , nucleation , combustion , inorganic chemistry , organic chemistry , paleontology , biology , physics , quantum mechanics
Chemical looping represents a novel approach for generating light olefins in which thermal cracking or catalytic dehydrogenation is coupled with selective hydrogen combustion (SHC) by a metal oxide redox catalyst, which enables autothermal operation, increased per‐pass conversion, and greater‐than‐equilibrium yields. Recent studies indicate that Na 2 WO 4 ‐promoted perovskite oxides are effective redox catalysts with high olefin selectivity. Herein, kinetic parameters, rates, and reaction models for the reduction of unpromoted and Na 2 WO 4 ‐promoted CaMnO 3 redox catalysts by H 2 , C 2 H 4 , and C 2 H 6 , is reported. Reduction rates of CaMnO 3 under ethylene and ethane are significantly lower than under H 2 . Model fitting of reduction kinetics show good agreement with reaction order–controlled models for CaMnO 3 reduction and predict greater oxygen site dependence and higher activation energy for CaMnO 3 reduction by C 2 H 4 as compared with H 2 . Avrami–Erofe'ev nucleation and growth models provide the best fit to the reduction of Na 2 WO 4 /CaMnO 3 in H 2 and in C 2 H 4 . After Na 2 WO 4 promotion, the reduction rate of CaMnO 3 is three orders of magnitude lower in ethylene in comparison to hydrogen, consistent with its superior selectivity to hydrogen combustion. The models developed can be applied toward reactor design and optimization in the context of enhanced olefin production via SHC under a cyclic redox scheme.

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