New kinetic model for the nanocrystalline anatase-to-rutile transformationrevealing rate dependence on number of particles

Existing kinetic models are unable to describe published experimental data for the anatase-to-rutile phase transformation in nanocrystalline samples. A new kinetic model is proposed that combines interface nucleation at certa in contact areas between two anatase particles and formation and growth of rutile nuclei. Kinetic equations, incorporating mass-balance considerations , derived for this "interface nucleation and constant growth" model fit the experimental data of Gribb and Banfield (1997) fairly well. Results confir m that the transformation is second order with respect to the number of par ticles of anatase. Over shorter reaction times, the net transformation rate is determined by the rate of nucleation, which is initiated from rutile-li ke structural elements in the contact area. The activation energy of 165.6 +/- 1.1 kJ/mol for rutile nucleation within nanocrystalline anatase particl es is much lower than values previously measured for rutile nucleation in c oarse anatase samples (>330 kJ/mol). Nuclei growth proceeds at a constant r ate with a very small activation barrier. Over longer reaction times, the n et transformation rate is determined both by nucleation and nuclei growth. Results quantitatively explain the origin of the size dependence of phase t ransformation rates in this system.