Abstract
The epitaxial overgrowth of brushite (CaHPO4·2H2O) by the interaction of phosphate-bearing, slightly acidic, aqueous solutions with gypsum (CaSO4·2H2O) was investigated in situ using atomic force microscopy (AFM). Brushite growth nuclei were not observed to form on the {010} gypsum cleavage surface, but instead formed in areas of high dissolution, laterally attached to gypsum [101] step edges. During the brushite overgrowth the structural relationships between brushite (Aa) and gypsum (A2/a) result in several phenomena, including the development of induced twofold twining, habit polarity, and topographic effects due to coalescence of like-oriented crystals. The observed brushite growth is markedly anisotropic, with the growth rate along the main periodic bond chains (PBCs) in the brushite structure increasing in the order [101] > [101] > [010], leading to tabular forms elongated on [101]. Such a growth habit may result from the stabilization of the polar [101] direction of brushite due to changes in hydration of calcium ions induced by the presence of sulfate in solution, which is consistent with the stabilization of the gypsum [101] steps during dissolution in the presence of HPO2-4 ions. The coupling between growth and dissolution was found to result in growth rate fluctuations controlled by the changes in the solution composition.
© 2015 by Walter de Gruyter Berlin/Boston
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Articles in the same Issue
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- Structure of nanocrystalline phyllomanganates produced by freshwater fungi
- First-principles study on variation of lattice parameters of mullite Al4+2xSi2–2xO10–x (x = 0.125, 0.250, 0.375)
- Natrolite may not be a “soda-stone” anymore: Structural study of fully K-, Rb-, and Cs-exchanged natrolite
- Metal retention, mineralogy, and design considerations of a mature permeable reactive barrier (PRB) for acidic mine water drainage in Northumberland, U.K.
- A relationship between d104 value and composition in the calcite-disordered dolomite solid-solution series
- XRD, micro-XANES, EMPA, and SIMS investigation on phlogopite single crystals from Mt. Vulture (Italy)
- Volume behavior of the 10 Å phase at high pressures and temperatures, with implications for H2O content
- Interfacial tension between immiscible liquids in the system K2O-FeO-Fe2O3-Al2O3-SiO2 and implications for the kinetics of silicate melt unmixing
- H2O and the dehydroxylation of phyllosilicates: An infrared spectroscopic study
- Effects of intermediate range structure on the 29Si NMR chemical shifts of framework silicates: Results for analcime
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