Abstract

Cu–Zn–Co–Al mixed oxides with different Cu : Zn : Co : Al atomic ratios have been obtained by thermal treatment of hydroxycarbonate precursors at different temperatures (623, 723, 823 and 973 K in air). The characterization has been performed by X-ray powder diffraction (XRPD), diffuse reflectance spectroscopy (DRS), thermal analysis (TG/DTA), BET surface-area determination and measurements of magnetic susceptibility. The XRPD patterns showed that the precursors were almost pure pillared-layered (PLS) hydrotalcite-like materials with general stoichiometric formula M6II M2III(OH)16CO3.4H2O (MII= Cu, Zn, Co, MIII= Al). The thermal decomposition of the precursors occurred in four steps, the first three (up to T= 673 K) consisting of complete dehydration of the sample, the fourth (843 ⩽T/K ⩽ 923) due to the release of CO2. The precursor structure collapsed at T⩽ 623 K, giving rise to poorly crystalline materials, in which the Cu2+ ions retained a distorted octahedral symmetry. Crystalline oxide mixtures were formed only after complete release of CO2. XRPD showed that the oxides obtained by calcination at 973 K consisted of a mixture of CuO, ZnO and spinels such as CuAl2O4, ZnAl2O4, ZnCo2O4, and/or spinel solid solutions. According to DRS and magnetic susceptibility, the formation of ZnCo2O4 seems to be privileged with respect to that of Co3O4 and ZnO.

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