Abstract

Synthetic talc is a new filler of industrial interest due to its submicron size, its chemical and mineral purity, and its hydrophilic character. To develop this filler on a preindustrial scale, this work aimed to understand the mechanisms of transformation from the amorphous talc precursor to crystalline synthetic talc. X-ray diffraction, Fourier transform infrared spectroscopy, and extended X-ray absorption fine structure at Ni–K edge techniques were used to study a Ni-talc series composed of a talc precursor sample and talc samples synthesized at 100, 200, and 300 °C for 1 or 6 h. As soon as the Ni-talc precursor precipitated, a tetrahedral–octahedral–tetrahedral-type structure appeared that was characterized by 2–3 Ni-octahedra distanced 3.07 A from each other and by 3–4 Si tetrahedra distributed on the top and bottom of the octahedral “sheet” and distanced 3.29 A from Ni. Simultaneously following the synthesis temperature, the octahedral sheet grew, and the tetrahedral sheet expanded; the distances Ni...

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