The kinetics and mechanisms of nanoparticulate amorphous calcium carbonate (ACC) crystallization to calcite, viavaterite, were studied at a range of environmentally relevant temperatures (7.5–25 °C) using synchrotron-based in situ time-resolved Energy Dispersive X-ray Diffraction (ED-XRD) in conjunction with high-resolution electron microscopy, ex situX-ray diffraction and infrared spectroscopy. The crystallization process occurs in two stages; firstly, the particles of ACC rapidly dehydrate and crystallize to form individual particles of vaterite; secondly, the vaterite transforms to calcitevia a dissolution and reprecipitation mechanism with the reaction rate controlled by the surface area of calcite. The second stage of the reaction is approximately 10 times slower than the first. Activation energies of calcite nucleation and crystallization are 73 ± 10 and 66 ± 2 kJ mol⁻¹, respectively. A model to calculate the degree of calcite crystallization from ACC at environmentally relevant temperatures (7.5–40 °C) is also presented.

Roundabout Gypsum: Calcium sulfates are a common but perhaps underappreciated group of minerals used in a number of natural and industrial processes. In many ways, these crystals precipitate from solution in the same way that most other aqueous minerals form; however, mounting evidence suggests that different, unexplored mechanisms may be at work. Van Driessche et al. (p. 69 ; see the cover) performed high-resolution microscopy of the most common calcium sulfate mineral, gypsum, at various points along time-resolved, fast-quenching growth experiments. The images reveal that gypsum particles actually start out as crystalline nanoparticles of another mineral, bassanite, which then self-assemble into well-ordered nanorods. Finally, the nanorods transform into gypsum following a hydration reaction. The observation that the reaction pathway occurs below the solubility limit of the intermediate phase has wide-ranging implications for biomineralization processes and may provide ways to prevent fouling on the surfaces of desalination membranes.