Structural, Microstructural and Vibrational Characterization of Apatite-type Lanthanum Silicates Prepared by Mechanical Milling
E. Rodriguez-Reyna; A.F. Fuentes; M. Maczka; J. Hanuza; K. Boulahya; U. Amador. Structural, Microstructural and Vibrational Characterization of Apatite-type Lanthanum Silicates Prepared by Mechanical Milling. Journal of Solid State Chemistry (ISSN: 0022-4596). 2006, Vol. 179, p. 522-2006.
Apatite-type lanthanum silicates have been successfully prepared at room temperature by dry milling hexagonal A-La2O3 and either amorphous or low cristobalite SiO2. Milling a stochiometric mixture of these chemicals in a planetary ball mill with a moderate rotating disc speed (350 rpm), allows the formation of the target phase after only 3 h although longer milling times are needed to eliminate all SiO2 and La2O3 traces. Thus, the mechanically activated chemical reaction proceeds faster when using amorphous silica instead of low cristobalite as silicon source and pure phases are obtained after only 9 and 18 h, respectively. As obtained powder phases are not amorphous and show an XRD pattern as well as IR and Raman bands characteristic of the lanthanum silicate. The domain size of the as-prepared phases varies gradually with the temperature of post-milling thermal treatment with activation energies of about 26(8) and 52(10) kJ mol-1K-1 for the apatites obtained from amorphous silica and low-cristobalite, respectively. These values suggest crystallite growth to be favored when using amorphous silica as reactant
Apatite-type lanthanum silicates have been successfully prepared at room temperature by dry milling hexagonal A-La2O3 and either amorphous or low cristobalite SiO2. Milling a stochiometric mixture of these chemicals in a planetary ball mill with a moderate rotating disc speed (350 rpm), allows the formation of the target phase after only 3 h although longer milling times are needed to eliminate all SiO2 and La2O3 traces. Thus, the mechanically activated chemical reaction proceeds faster when using amorphous silica instead of low cristobalite as silicon source and pure phases are obtained after only 9 and 18 h, respectively. As obtained powder phases are not amorphous and show an XRD pattern as well as IR and Raman bands characteristic of the lanthanum silicate. The domain size of the as-prepared phases varies gradually with the temperature of post-milling thermal treatment with activation energies of about 26(8) and 52(10) kJ mol-1K-1 for the apatites obtained from amorphous silica and low-cristobalite, respectively. These values suggest crystallite growth to be favored when using amorphous silica as reactant