The reconstruction of layered double hydroxides with the hydrotalcite-like structure from material previously calcined at increasing temperatures has been studied. Both the calcination temperature and the time the samples spent equilibrating with a controlled water vapour pressure have been considered. The crystallinity of the samples and the crystalline phases formed have been assessed by powder X-ray diffraction, while the local environment of the Al ions has been probed by 27 A1 MAS NMR. It has been found that reconstruction is complete when the sample has been calcined at or below 550 °C, after 24 h rehydration, while equilibration for 3 days is adequate to reconstruct samples previously calcined at 750 °C. Only partial reconstruction is observed after calcination at 1000 °C. However, the NMR results indicate that, in all cases, some of the Al ions remain in tetrahedral sites.
Layered double hydroxides (LDHs) with the hydrotalcite-like structure have been prepared containing different amounts of Ni2+, Cu2+ and Al3+ in the brucite-like layers by a coprecipitation method. The samples have been characterized by elemental chemical analysis, powder X-ray diffraction, differential thermal analysis and thermogravimetric analysis, FT-IR and UV–VIS diffuse reflectance spectroscopies, temperature-programmed reduction, and specific surface area and porosity assessment by N2 adsorption at −196 °C. The nature of the phase obtained, crystallinity of the HT-like phase and thermal behaviour of these materials were influenced by MII/Al atomic composition and concentration of bivalent metal ion. Calcination at 500 °C leads to mostly amorphous solids containing NiO, and also CuO (tenorite) for large Cu2+ contents (Cu/Ni molar ratio equal to 4). When the calcination temperature is increased to 850 °C, crystallization of well defined phases (NiO, CuO and NiAl2O4, depending on the relative amounts of Ni, Cu and Al) takes place. Reduction of Cu2+ species in these samples takes place at a lower temperature than that for Ni2+, while the temperature of reduction of nickel is increased with an increase in aluminium and copper content of the samples.