ELECTROCHEMICAL SYNTHESIS OF DISPERSED BARIUM FERRITE USING ANODIC DISSOLUTION OF METAL

The process of anodic dissolution of iron (purity not less than 99%) in aqueous solutions of barium chloride, barium nitrate and binary electrolytes under galvanostatic conditions and by registration of potentiodynamic polarization curves was investigated. The influence of solution composition and concentration and the value of applied direct current on the intensity of anodic oxidation of iron was shown. It was revealed that the oxidation rate of metal in binary electrolytes containing barium chloride and barium nitrate is comparable with the intensity of anodic dissolution in a solution based on barium chloride. It was found that anodic polarization curve in solutions containing BaCl2 and Ba(NO3)2 has a complex form typical of passivated metals. There is a clear maximum of anodic oxidation current on this curve, as well as in barium nitrate solution, however the peak height is much higher (50-150 times). A method for the synthesis of dispersed barium ferrite, based on the anodic oxidation of iron in aqueous barium chloride and barium nitrate solutions with subsequent thermal treatment of the product of electrochemical dissolution was suggested. The phase and elemental composition and structural characteristics of obtained precursor and ferrite samples were examined using X-ray phase analysis. The influence of the heat treatment mode on the phase composition of the synthesized samples is shown. It is found that electrolysis with a soluble iron electrode using direct anode current in 0.05M BaCl2 + 0.5M Ba(NO3)2 solution and subsequent thermal treatment of the dissolution product at 1200 ° C provide the formation of dispersed system, whose phase composition is predominantly Ba0.87Fe11.08O17.15 (74%) and BaFe2O4 (17%).