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Title: Investigation of gas-solid reaction kinetics in iron compounds

Technical Report ·
OSTI ID:5752205

Studied were the hydrogen reduction of FeO, the cyclic reduction and oxidation of Fe/sub 2/O/sub 3/ using hydrogen and dry air as the reacting gases, and the oxidation of FeS in dry flowing air. The decomposition of Fe/sub 2/(SO/sub 4/)/sub 3/ in air and the oxidation of iron reduced from FeO were also investigated. The direct hydrogen reduction of FeO and Fe/sub 2/O/sub 3/ powder between 723 and 873/sup 0/K led to sigmoid-shaped curves on which a zero-order kinetic expression was employed. A critical temperature effect was observed at 803/sup 0/K for the reduction of FeO. Activation energies of 58 and 51 kJ/mol were calculated for the low and high temperature reduction of FeO. A similar value of 53 +- 4 kJ/mol was derived for Fe/sub 2/O/sub 3/ reduction. Cycling was found to reduce the rates of both the reduction and oxidation reactions in Fe/sub 2/O/sub 3/. The oxidation of FeS is complex. A model is proposed, and the various observations are discussed in terms of a sequence of solid-state and gas-solid reactions. The oxidation of stoichiometric FeS (troilite) between 648 and 923/sup 0/K led to a final product of Fe/sub 2/O/sub 3/ as well as a variety of intermediate compounds which included Fe/sub 1-x/S (pyrrhotite), FeS/sub 2/ (pyrite), Fe/sub 2/(SO/sub 4/)/sub 3/, and Fe/sub 3/O/sub 4/ (magnetite). Oxidation kinetics at intermediate temperatures were controlled by the Fe/sub 2/(SO/sub 4/)/sub 3/ formation and decomposition. The activation energies for FeS oxidation and Fe/sub 2/(SO/sub 4/)/sub 3/ decomposition are 192 kJ/mol and 219 kJ/mol.

Research Organization:
California Univ., Davis (USA)
DOE Contract Number:
AS03-80ER10708
OSTI ID:
5752205
Report Number(s):
DOE/ER/10708-T5; ON: DE86012296
Resource Relation:
Other Information: Portions of this document are illegible in microfiche products. Thesis
Country of Publication:
United States
Language:
English