In this study, the feasibility of producing electrolytic iron from red muds in a strongly alkaline medium at 110 °C was studied. The red mud samples from a French industry were characterized by various techniques (ICP-AES, SEM, XRD) to determine their chemical and mineralogical compositions. The main phase in the red mud investigated was hematite (α-Fe2O3). Iron electrodeposition tests from red mud suspended in a 12.5 mol/L NaOH electrolyte were conducted at constant current in a stirred electrochemical cell. The solid:liquid ratio and amounts of impurities contained in red mud were varied to optimize the faradaic yield and the production rate of electrolytic iron. Whereas hematite can be reduced to iron with a current efficiency over 80% for a current density (cd) up to 1000 A/m 2 , the current efficiency with red muds was highest for a cd below 50 A/m 2 and then decreased regularly to 20% at 1000 A/m 2 . In all cases, the deposit produced contained more than 97% metal iron. The moderate performance of the process investigated with red mud was attributed to a troublesome adsorption of red mud particles on the cathode, making the reduction far less efficient than that with hematite.
<p class="PaperAbstract"><span lang="EN-GB">Iron can be produced by the direct electrochemical reduction of hematite particles suspended in hot, concentrated NaOH solutions. Because various other iron sources can be considered, the present work was aimed at investigating the electrolytic treatment of the “red mud” generated by the Bayer process for alumina preparation from bauxite. Such sources contain very high amounts of impurities, in particular silicon and aluminium oxide-based minerals, in addition to other mineral phases. Electrolytic reductive treatment of the industrial red mud sample was shown to be possible but with both lower current density and current efficiency than for pure hematite. After deposition tests at a fixed current density, further experiments in simulation tests have been carried out for better understanding. In particular, hematite particles were tested with and without impurities introduced in the solution. Presence of little soluble impurities at the particle surface appear to hinder the reactivity of the suspended particles at the cathode surface, whereas side-hydrogen reaction still occurs. </span></p>
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