Objectives. To obtain highly dispersed powders of chromium(III) molybdate Cr2(MoO4)3 by solid phase synthesis and to study their porous structure.Methods. After stirring in water, a mixture of Cr2O3 and MoO3 oxide powders was dried in air and subjected to heat treatment in the temperature range of 600–800°C. After heat treatment, the products were identified by X-ray phase and sedimentation analysis. The specific surface area was measured using the Brunauer–Emmett–Teller static adsorption method. Porosity parameters were measured using the Barrett–Joyner–Halenda (BJH) method.Results. The Gibbs free energy ΔG of the reaction between chromium and molybdenum oxides was calculated and it was shown that the process is characterized by a significant negative value of ΔG. Concurrently, the Gibbs energy exhibits a relatively weak dependence on temperature. The highly dispersed chromium(III) molybdate powders with specific surface area of 15.3–29.7 m2·g−1 obtained in this way were pure according to X-ray diffraction analysis. A study of the volume, diameter, and pore size distribution was conducted through the utilization of nitrogen adsorption–desorption isotherms in accordance with the BJH model.Conclusions. It was demonstrated that Cr2(MoO4)3 powders possess a mesoporous structure and are distinguished by a bimodal pore system comprising small pores with a diameter of 2–3 nm and larger pores with a diameter ranging from 15 to 30 nm.
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