Abstract

In the systems CoO–Al 2O 3–SiO 2–H 2O and CoO–Al 2O 3–SiO 2–HCl–H 2O, at initial pH between 5.5 and 8.1 and temperature of 200 °C, kaolinite is unstable and the following phases form through a dissolution-precipitation process: a) kaolinite and Co-bearing kaolinite; b) Al–Co–serpentine; and c) poorly crystalline phases. Identification of the several phases was carried out from a combination of X-ray diffraction and transmission/analytical electron microscopy. Co–kaolinite shows variable morphologies: a) Platy lath-shaped particles with very low Co content; b) Spherical particles, with relatively constant Co contents (in the order of 0.10 apfu); c) Kaolinite stacks with very variable Co contents (up to 0.25 apfu). Analytical data indicate that the presence of Co(OH) 2 in the system favors the dissolution process as well as serpentine formation but it leads to the parallel formation of abundant poorly crystalline phases. The Co-content in kaolinite increased as a function of the Co(OH) 2/CoCl 2 ratio in the initial systems, and it is reflected by a parallel increase of the b-cell parameter of kaolinite. The average composition of the coexisting Al–Co–serpentine is: (Al 1.20Fe 0.11Co 1.27)(Si 1.64Al 0.36)O 5(OH,Cl) 2, with Cl contents in the order of 0.14 apfu. The assemblage Co–kaolinite + Al–Co–serpentine, which appears to be stable at 200 °C, has not been described in natural environments, probably because it requires unusual Al- and Co-rich chemical systems.

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