Amorphous calcium carbonate (ACC) is a common transient precursor to biogenic crystalline calcium carbonate, but factors controlling the amorphous to crystalline transformation remain unclear. We present a structural analysis and comparison of hydrated and partially dehydrated, synthetic ACC samples. Thermogravimetric analysis showed total H 2 O losses of 46% with heating to 115 °C and 75% for heating to 150 °C. The 1 H NMR spectra of hydrous ACC, obtained both directly and indirectly, via 13 C-detection, contain signals from four principal hydrogen environments: translationally rigid structural H 2 O, a restrictedly mobile H 2 O environment, fluidlike mobile H 2 O that is decoupled from rigid H and C, and hydroxyl. The retention of some restrictedly mobile H 2 O and lack of change in X-ray total scattering and absorption spectroscopy data for dehydrated ACC suggest that thermal dehydration does not significantly disrupt the calcium-rich ACC framework. NMR results and thermal analyses of samples dehydrated isothermally for extended periods indicate that the H 2 O loss mechanism is kinetically hindered and occurs in three stages: simultaneous loss of fluidlike mobile, restrictedly mobile, and rigid H 2 O → loss of restrictedly mobile and rigid H 2 O → loss of hydroxyl and trapped rigid and mobile components that cannot be removed without transformation to crystalline calcium carbonate.
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Schmidt et al. (2014) studied this question.
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