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Journal ArticleDOI

Kinetics of the reduction of bushveld complex chromite ore at 1416 °C

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TLDR
In this article, a generalized rate model based on an ionic diffusion mechanism was developed to satisfactorily describe the solid-state carbothermic reduction of chromite, which included the contribution of the interfacial area between partially reduced and unreduced zones in chromite particles and diffusion.
Abstract
The kinetics of the reduction of chromite ore from the LG-6 layer of the Bushveld Complex of the Transvaal in South Africa were studied at 1416 °C by the thermogravimetric analysis (TGA) technique. Spectroscopic graphite powder was employed as the reductant. The aim of this article is to present a kinetic model that satisfactorily describes the solid-state carbothermic reduction of chromite. A generalized rate model based on an ionic diffusion mechanism was developed. The model included the contribution of the interfacial area between partially reduced and unreduced zones in chromite particles and diffusion. The kinetic model described the process for degrees of reduction from 10 to 75 pet satisfactorily. It was observed that at a given particle size, the rate of reduction was controlled mainly by interfacial area up to about 40 pet reduction, after which the rate was dominated by diffusion. On the other hand, for a given degree of reduction, the contribution of the interfacial area to the rate increased, while that of diffusion decreased, with a decrease in the particle size. The value of the diffusion coefficient for the Fe2+ species at 1416 °C was calculated to be 2.63 x 10-2 cm2/s.

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Citations
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Journal ArticleDOI

Solid state reduction of a natural ilmenite

TL;DR: In this article, an ilmenite concentrate was reduced with graphite under argon gas between 1250 and 1350°C by using a thermogravimetric analysis (TGA) system.
Journal ArticleDOI

Investigations on the carbothermic reduction of chromite ores

TL;DR: In this paper, the reduction of chromite ores using different reducing carbonaceous reducing agents in the temperature range 1173 to 1573 K was investigated and the activation energy for this process was estimated to be 130 kJ/mole.
Journal ArticleDOI

The reduction of chromite in the presence of silica flux

TL;DR: In this article, the mechanism and kinetics of the carbothermic reduction of a natural chromite was studied at 1300-1500°C in the presence of silica, and a two stage reduction mechanism was established.
Journal ArticleDOI

Catalytic reduction of carbon-chromite composite pellets by lime

TL;DR: In this paper, the authors investigated the catalytic effect of lime on the reduction of carbon-chromite composite pellets at 1270-1433°C under CO-argon atmospheres, and found that the data for the early stage of reduction fit both an exponential law for nucleation control and an equation for chemical control with an apparent activation energy ranging from 139 to 161 kJ/mol depending on the amount of lime addition.
Journal ArticleDOI

The reduction mechanism of chromite in the presence of a silica flux

TL;DR: The reduction behavior of a natural chromite from the Bushveld Complex of South Africa was studied at 1300 °C to 1500 °C in this paper, where graphite was reduced by graphite in the presence of silica.
References
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Journal ArticleDOI

The reduction mechanism of a natural chromite at 1416 °C

TL;DR: In this paper, the behavior of a natural chromite from the Bushveld Complex, Transvaal, South Africa, during reduction at 1416 °C by graphite was studied by means of thermogravimetric analysis, X-ray diffraction (XRD) analysis, energy-dispersive Xray analysis (EDAX), and metallographic analysis.
Journal ArticleDOI

Diffusion of Cobalt and Chromium in Chromite Spinel

R. Sun
TL;DR: The diffusion of cobalt and chromium in sintered samples of CoCr2O4 has been measured in the temperature region 1400°C-1600°C where it is believed that bulk diffusion predominates.
Journal ArticleDOI

An ionic diffusion mechanism of chromite reduction

TL;DR: In this article, the formation of a slightly iron-enriched core comprising distorted spinel unit cells surrounded by a region of normal spinel units, effected by the reduction of Fe3+ to Fe2+, and formation of Cr-Al sesquioxide and Mg-Cr-Al spinel phases.
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