Abstract

Spherical particles (∼3 μm) of copper(II) oxalate were produced in the form of precipitated solids by gently mixing aqueous solutions of oxalic acid and copper nitrate with predetermined concentrations at room temperature. These particles were isolated from the mother liquor and then coated with cobalt basic carbonate. The coating trials involved heating of the aqueous dispersions, containing known amounts of the dispersed copper oxalate particles (cores), urea, and cobalt nitrate, at 70–85 °C for various periods of time with constant stirring. The heating process decomposed urea, increased pH, liberated carbonate ions, which resulted in the precipitation of the dissolved cobalt ions in the form of shells of cobalt basic carbonate around each core particle. The coating process was sensitive to the applied experimental parameters, since uniformly coated particles were obtained under a narrow range of coating mixture composition. In the absence of the cores, the same reactants solutions produced coating precursor particles (cobalt basic carbonate), when subjected to similar heating conditions. Physical and chemical analyses indicated that the coating material of the coated particles and the coating precursor particles had the same chemical compositions. The as-prepared core, coating precursor, and coated particles were converted into oxide forms by heating their dry powders at elevated temperatures under controlled heating conditions. The heat treatment produced obvious changes in the surface morphology of these particles due to loss of material. Moreover, the heat-treated particles preserved shape integrity to a maximum extent, showing their thermal stability. Selected batches of the as-prepared and heat-treated products were characterized by various physical methods.

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