Chemistry:Hydrohalite
| Hydrohalite | |
|---|---|
| General | |
| Category | Halide mineral |
| Formula (repeating unit) | NaCl·2H2O |
| Strunz classification | 3.BA.05 |
| Crystal system | Monoclinic |
| Crystal class | Prismatic (2/m) (same H-M symbol) |
| Space group | P21/c |
| Identification | |
| Colour | Colourless or white |
| Diaphaneity | Transparent |
Hydrohalite is a mineral that occurs in saturated halite brines at cold temperatures (below 0.1 °C). It was first described in 1847 in Dürrnberg, Austria. It exists in cold weather.
Hydrohalite has a high nucleation energy, and solutions will normally need to be supercooled for crystals to form. The cryohydric point is at −21.2 °C (−6.2 °F). Above this temperature, liquid water saturated with salt can exist in equilibrium with hydrohalite. Hydrohalite has a strong positive temperature coefficient of solubility, unlike halite.[2] Hydrohalite decomposes at 0.1°C, giving a salty brine and solid halite. Under pressure, hydrohalite is stable between 7,900 and 11,600 atmospheres pressure. The decomposition point increases at the rate of 0.007K per atmosphere (for 1–1000 atmospheres).[2] The maximum decomposition temperature is at 25.8°C under 9400 atmospheres. Above this pressure the decomposition point goes down.[2]
Ceres
Hydrohalite was discovered on Ceres by Dawn,[3] suggesting an early ocean, possibly surviving as a relict ocean.
References
- ↑ Warr, L.N. (2021). "IMA–CNMNC approved mineral symbols". Mineralogical Magazine 85 (3): 291–320. doi:10.1180/mgm.2021.43. Bibcode: 2021MinM...85..291W.
- ↑ 2.0 2.1 2.2 Braitsch, O. (1971). "The Stability Conditions of Salt Minerals". Salt Deposits Their Origin and Composition. Springer. pp. 42–44. doi:10.1007/978-3-642-65083-3_2. ISBN 978-3-642-65085-7.
- ↑ De Sanctis, M.C., Ammannito, E., Raponi, A. et al. Fresh emplacement of hydrated sodium chloride on Ceres from ascending salty fluids. Nat Astron 4, 786–793 (2020). https://doi.org/10.1038/s41550-020-1138-8
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