Thermodynamic aspects of Cr<sub>2</sub>O<sub>3</sub> reduction by carbon

Abstract

In order to save resources of chromium, technology of flux-cored wire surfacing is of great practical interest. In this case Cr2O3 chromium oxide and carbon as a reducing agent are used as fillers. Thermodynamic assessment of probability of 16 reactions between them under standard conditions and for certain reactions under conditions different from standard was carried out using tabulated thermodynamic data of reactants in temperature range of 1500 – 3500 K. The following states were considered as standard states for reactants: Cr(ref) (reference state, melting point 2130 K, boiling point 2952 K), Cr(liq), Cr(gas), Cr2O3 (cr, liq), Cr2O3 (gas), C(ref), and as possible reaction products and standard states for them CO(gas), CO2 (gas), Cr23C6 (сr), Cr7C3 (cr), Cr3C2 (cr). Probability of reactions was estimated using standard Gibbs energy and the Gibbs energy calculated using the Van Goff isotherm equation. Dissolution of chromium in metal of surfacing bath or probable partial pressures of CO and CO2 in gas phase was taken into account and was calculated from equilibrium of carbon gasification reaction. Presence of carbon in flux-cored wire with chromium oxide Cr2O3 as a reducing agent will necessarily lead to occurrence of reduction reactions with generation of chromium carbides, and possibly chromium itself. Generation of Cr7C3 (сr) carbide is likely. With longer life time of chromium oxide and carbon at a temperature above 2500 K, generation of chromium as a component of the surfacing bath is more thermodynamically probable than generation of its carbides. Chromium oxide has the highest reactivity in Cr2O3 (liq) state. Direct reduction is preferential. Generation of CO(gas) as a product of carbon oxidation is more probable. Dissolution of chromium in metal increases thermodynamic probability of reactions with its generation and further reduces probability of reactions in which chromium is the starting material.