Croatica Chemica Acta, Vol. 69 No. 1, 1996.
Izvorni znanstveni članak
Formation of ZrO2 by the Thermal Decomposition of Zirconium Salts
Goran Štefanić
; Ruđer Bošković Institute, P. O. Box 1016, 10001 Zagreb, Croatia
Svetozar Musić
; Ruđer Bošković Institute, P. O. Box 1016, 10001 Zagreb, Croatia
Stanko Popović
; Ruđer Bošković Institute, P. O. Box 1016, 10001 Zagreb, Croatia
Krešimir Furić
; Ruđer Bošković Institute, P. O. Box 1016, 10001 Zagreb, Croatia
Sažetak
Hydrated zirconium salts containing Cl- , NO3- or SO42- anions were thermally treated up to 1300 °C. The thermal decomposition products were investigated using the X-ray diffraction (XRD), Fourier transform IR spectroscopy (FT-IR) and laser Raman spectroscopy. The thermal decomposition products of all three zirconium salts, characterized as amorphous material, showed a maximum of X-ray scattering at -16° and also in the corresponding FT-IR spectra a broad band at 450 cm-1. With an increase of the heating temperature of all three salts (400 °C for ZrOCl2 ∙ 8H2O, 400 °C for ZrO(NO3)2 ∙ 2H2O and 700 °C for Zr(SO4)2 ∙ 4H2O), the metastable f-ZrC>2 was formed, which disappeared on further heating to higher temperatures. The yield of f-ZrC>2, measured by XRD, depended on the nature of the starting salt, and the highest value was obtained for ZrOCl2 ∙ 8H2O salt. The t-ZrO2 phase formed from ZrOCl2 ∙ 8H2O was thermally most unstable, while the presence of a small amount of t-ZrO2 was observed in the thermal decomposition product obtained by heating Zr(SO4)2 ∙ 4H2O even at 1300 °C. Metastable t-ZrO2, generated by the thermal decomposition of ZrOCl2 ∙ 8H2O or ZrO(NO3)2 ∙ 2H2O salt, was highly sensitive to mechanical treatment, while metastable t-ZrO2 formed from Zr(SO4)2 ∙ 4H2O was stable during the same process. The nature of the starting salt influenced the formation of metastable t-ZrO2, however, when t-ZrO2 was once formed, its stability depended on the anionic impurities that remained in the oxide material.
Ključne riječi
Hrčak ID:
135956
URI
Datum izdavanja:
4.3.1996.
Posjeta: 2.354 *