Abstract
A series of new-generation synthetic talcs were prepared by varying the hydrothermal synthesis duration from a few hours up to 2 months. Crystallinity and particle size analysis of the synthetic products were evaluated by photon correlation spectroscopy, transmission electron microscopy, differential thermal analysis and unoriented X-ray diffraction, and then analyzed by various spectroscopic methods such as Fourier transformed infrared spectroscopy and solid-state 1H and 29Si magic angle spinning nuclear magnetic resonance. The new process for preparing synthetic talcs allows to obtain single-phased particles which after few hours grow heterogeneously and simultaneously in both the c* direction and the (ab) plan. Fine particles, observed for whatever the synthesis duration, lead to the presence of numerous sheet edges surfaces due to particle size which represents the main difference with natural talc. Spectroscopy data show the influence of the fine particles on signals and highlight that synthetic talc characterization is a potential tool for better understanding crystal chemistry of natural talc.
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