Abstract

In recent years, the preparation of CMAS nanocrystalline glass-ceramics has shown potential as an application of secondary resourcing technology in utilizing Bayan Obo iron ore tailings containing rare earth elements. The crystallization mechanism for nanodiopside-type glass-ceramics was studied via an investigation of the nonisothermal crystallization kinetics of the glass system, combined with the in situ observation of softening and crystallization of the basic glass using a high-temperature laser confocal microscope. The results show that the activation energy of nucleation in the glass system is higher than that of crystal growth by using the Ozawa model. The crystallization mechanism changes as the crystallization fraction increases, that is, from the three-dimensional growth in which the nucleation rate increases with time in an interface-controlled manner (a > 1, b = 1, m = 3) at the initial stage of crystallization to a decreased nucleation rate in a diffusion-controlled growth (a = 0.5, b = 0.5, m = 3) at the middle and later stages. This process involves both surface crystallization and volume crystallization. The crystallization was observed in situ, and it was further confirmed that there exists a critical nucleation temperature between Tg and Tx, which is related to the interface free energy and critical Gibbs free energy difference. When the temperature exceeds the critical value of Tg + 55 K, the system begins to exhibit visible crystallization. With an increase in temperature, the basic glass softened considerably, while the crystal grew significantly. In addition, the surface roughness can be used to characterize the crystallization process, providing a new research method for crystal growth.

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