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An idea of vacuum suction through a porous graphite tube has been applied to maintain direct contact between FeObearing molten slag and graphite by continuous removal of COgas generated by the reduction, In th!s way examination of relative importance of the direct and indirect reductions has become possible.

The effect of addition of small amounts of aluminium on mechano‐chemical reduction of hematite by graphite was studied. Various amounts of aluminium (0 to 10%) were added to a hematite‐graphite mixture, in which C/O ratio was 1:1. The hematite‐graphite‐aluminium mixtures were then subjected to ball milling followed by heating up reduction. The heating up reduction was carried out in Ar atmosphere, using TG‐DTA device. In TG‐DTA experiments, samples were heated by a constant heating rate of 10 °C/min from room temperature up to 1100 °C and maintained for 30 minutes at this temperature. To clarify the reactions which took place during milling and heating up reduction, the samples were subjected to XRD examinations. It was found that the heat generated during exothermic reaction of aluminothermic reduction of hematite promoted the endothermic reaction of carbothermic reduction. In the course of heating up reduction, the carbothermic reaction occurred just after aluminothermic reaction. Increasing of aluminum content from 0 to 10% in 2 hours ball milled samples decreased the temperature of carbothermic reaction from 1020 °C to about 860 °C. The further ball milling of the samples up to 5 and 10 hours, for the samples containing 10 and 5% aluminium respectively, caused the decrease of the temperature of aluminothermic and carbothermic reactions to around the melting point of aluminium.

A ZrSiO4/B2O3/Mg/C system was used to synthesize a ZrB2‐based composite through a high‐energy ball milling process. As a result of the milling process, a mechanically induced self‐sustaining reaction (MSR) was achieved in this system. A composite powder of ZrB2–SiC–ZrC was prepared in situ by a magnesiothermic reduction with an ignition time of approximately 6 min. The mechanism for the formation of the product was investigated by studying the relevant subreactions, the stoichiometric amount of B2O3, and thermal analysis.