Carbothermic Reduction of Alumina into a Metallic Solvent Phase (ABSTRACT PAGE)

- Organization:
- International Mineral Processing Congress
- Pages:
- 1
- File Size:
- 108 KB
- Publication Date:
- Jan 1, 2003
Abstract
The principle of carbothermic reduction has been around for many years. In principle it is a simple process, yet with a multitude of problems. The temperature required to affect reduction is in the region of 2200ºC and results in aluminium oxy-carbide formation rather than metallic aluminium. From a thermodynamic point of view, reducing the temperatures of reaction which would suppress oxy-carbide formation would only be possible by lowering the total pressure of the system. A decrease in thermodynamic activity of product aluminium by dissolving it in another phase would also help preventing the formation of oxy-carbides and would also increase the yield of the reduction reaction. Thus experiments have been conducted at around 1700ºC to determine the possibility of carbothermic reduction of alumina under the presence of a metallic solvent. Total pressure of the system was reduced to around 30kPa and metallic nickel, iron, copper and tin were selected as the solvent. The highest recovery of aluminium was achieved with the nickel solvent followed by iron, copper and tin. This ranking for the first three was also in accord with the extent of negative deviation form ideality in the respective binary solutions of these solvents with aluminium. The tin-aluminium system displays positive deviation form ideality. The rate and extent of reduction was found to be highly dependent on temperature and pressure. The pseudo first order reaction rate was found to be applicable to the process in all the solvents used. Rate constants were calculated and it is also suggested that the reduction was controlled primarily by the chemical reaction rate.
Citation
APA:
(2003) Carbothermic Reduction of Alumina into a Metallic Solvent Phase (ABSTRACT PAGE)MLA: Carbothermic Reduction of Alumina into a Metallic Solvent Phase (ABSTRACT PAGE). International Mineral Processing Congress, 2003.