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Reactions in the system CaO-MgO-SiO2-H2O. Hydrothermal treatment of some compositions on the joins Ca3Si2O7-Mg3Si2O7 and Ca2SiO4-Mg2SiO4

Published online by Cambridge University Press:  05 July 2018

K. Speakman*
Affiliation:
The Building Research Station, Garston, Watford

Summary

The effects of hydrothermal treatments on gel mixtures and synthetic minerals in the C3S2-M3S2 and C2S-M2S regions of the CaO-MgO-SiO2 system have been investigated. The products formed in the temperature range 180-350°C at pressures up to 220 N/mm2 were identified. The reactants generally behaved as simple mixtures of binary silicates and their products agreed well with existing data for reactions in the CaO-SiO2-H2O and MgO-SiO2-H2O systems. An unidentified phase that resulted from the hydration of åkermanite could be a new compound in the quaternary CaO-MgO-SiO2-H2O system. There was no evidence to indicate that a magnesium analogue of kilchoanite can be formed from materials that are isostructural with γ-Ca2SiO4.

Type
Research Article
Copyright
Copyright © The Mineralogical Society of Great Britain and Ireland 1970

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References

Barrer, (R. M.), 1948. Journ. Chem. Soc. 127 (and later papers).Google Scholar
Bowen, (N. L.) and Tuttle, (O. F.), 1949. Bull Geol. Soc. Amer. 60, 439-60.CrossRefGoogle Scholar
[Budnikov, (P. P.), Gorshkov, (V. S.), and Khmelevskaya, (T. A.)]. , 1960. (Building Materials) 6 (5) 2933.Google Scholar
[Butt, (Yu. M.), Astreeva, (O. M.), and Krasnoslobodskaya, (Z. S.)]. , 1960. (Cement), 26 (3) 813.Google Scholar
[Gorshkov, (V. S.) and Khmelevskaya, (T. A.)]. , 1960. (Coll. reports All-Union sci.-invest, building materials), 2, 75129.Google Scholar
Kalousek, (G. L.) and Mui, (D.), 1954. Journ. Amer. Ceram. Soc. 37 (2), 3841.CrossRefGoogle Scholar
Kitahara, (S.), Takenouchi, (S.), and Kennedy, (G. C.), 1966. Amer. Journ. Sci. 264, 223-33.CrossRefGoogle Scholar
Morey, (G. W.) and Ingerson, (E.), 1937. Amer. Min. 22, 1121.Google Scholar
Nolan, (J.), 1966. Quart. Journ. Geol. Soc. 122 (486), 119-57.CrossRefGoogle Scholar
Nolan, (J.) and Edgar, (A. D.), 1963. Min. Mag. 33, 625-34.Google Scholar
Roy, (D. M.) and Harker, (R. I.), 1960. Proc. 4th Int. Syrup. Chem. Cement, 196-20l.Google Scholar
Roy, (D. M.) and Johnson, (A. M.), 1965. Proc. Int. Syrup. Autoclaved Calcium Silicate Building Products, London, 114-21.Google Scholar
Roy, (R.) and Osborn, (E. F.), 1952. Econ. Geol. 47, 717.CrossRefGoogle Scholar
Speakman, (K.), 1968. Trans. Brit. Ceram. Soc. 67 (6), 233-42.Google Scholar
Speakman, (K.) and Taylor, (H. F. W.), 1965. Proc. Int. Symp. Autoclaved Calchtm Silicate Building Products, London, 142-7.Google Scholar
Speakman, (K.) and Taylor, (H. F. W.), 1967. Journ. Chem. Soc. 1052-60.Google Scholar
Taylor, (H. F. W.), 1960. Proc. 4th Int. Syrup. Chem. Cement, 167-90.Google Scholar
Taylor, (H. F. W.), 1964. The Chemistry of Cements (Academic Press,) 167232.Google Scholar