Abstract
This study investigated the incorporation of hydrogen (H2) as a partial replacement of carbon (C) during ferrochrome (FeCr) production. Chromite was subjected to H2-reduction to metallise its iron (Fe) −oxide content, followed by the removal of the metallised Fe by acid leaching. Hereafter, the chromium (Cr) −oxide rich ore was subjected to C-reduction. During H2-reduction, 64.3 % ± 6.1 % of Fe-oxides could be metallise, whereas C-reduction metallised the remaining Fe-oxides, as well as the Cr-oxide constituency. The C-reduction at 1300 °C resulted in near-complete metallisation of both the Fe- and Cr-oxide constituencies. By following this route, C emissions were reduced by approximately 16 %. It was further determined the process followed a shrinking core model. This model was confirmed by sub-surface microscopy, which highlighted the formation of a metallic layer at the chromite particle surface. This layer formation was evident during both H2- and C-reduction. It was also found that during the implemented Fe removal process that decrepitation of the H2-treated ore occurred. Mineralogical analysis of the H2-reduced and leached chromite suggests the formation of an eskolaite-type phase. Subsequent removal of the metallised Cr resulted in a MgAl2O4 spinel-type phase, which suggests that the majority of Fe and Cr were removed. These findings provide comprehensive insights into the chemical, physical, and mineralogical transformations of chromite during reduction and leaching, offering valuable implications for the decarburisation of FeCr production.