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Title: The reduction of iron oxides by volatiles in a rotary hearth furnace process: Part I. The role and kinetics of volatile reduction

Journal Article · · Metallurgical and Materials Transactions B: Process Metallurgy and Materials Processing Science
;  [1]
  1. Carnegie Mellon University, Pittsburgh, PA (United States)

With iron ore reduction processes using coal-ore pellets or mixtures, it is possible that volatiles can contribute to reduction. By simulating the constituents of the individual reducing species in the volatiles, the rates for H{sub 2} and CO were investigated in the temperature and reduction range of interest; hydrogen is the major reductant and was studied in detail. The kinetics of the reduction by H{sub 2} has been found to be a complex mechanism with, initially, nucleation and growth controlling the rate. There is a catalytic effect by the existing iron nuclei, followed by a mixed control of chemical kinetics and pore diffusion. This results in a topochemical reduction of these iron oxide particles. Up to 1173 K, reduction by H{sub 2} is considerably faster than by carbon in the pellet/mixture or by CO. It was also found that H{sub 2}S, which is involved with the volatiles, does not affect the rate at the reduction range of interest.

OSTI ID:
20674664
Journal Information:
Metallurgical and Materials Transactions B: Process Metallurgy and Materials Processing Science, Vol. 36, Issue 5; ISSN 1073-5615
Country of Publication:
United States
Language:
English

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