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Gyrolite

Published online by Cambridge University Press:  14 March 2018

A. L. Mackay
Affiliation:
Birkbeck College Research Laboratory, University of London
H. F. W. Taylor
Affiliation:
Birkbeck College Research Laboratory, University of London

Extract

The mineral gyrolite was discovered in Skye by T. Anderson in 1851. He showeditto be ahydratedcaleiumsilicateofapproximate composition 2CaO.3SiO2.3H2O. Subsequently gyrolite has been found in other localities, and has been prepared hydrothermally by Flint, McMurdie, and Wells. The ratio of lime to silica found by Anderson appears well established, but various values of the water content have been reported and more recent analyses approximate to 2CaO.3SiO2.2H2O. X-ray powder measurements were given by McMurdie and Flint, a but no crystallographic or other investigations of a detailed character have been reported.

Type
Research Article
Copyright
Copyright © The Mineralogical Society of Great Britain and Ireland 1953

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References

page 80 note 1. Anderson, T., Phil Mag., 1851, ser. 4, vol. 1, p. 111 CrossRefGoogle Scholar.

page 80 note 2. Flint, E. P., McMurdie, H. F., and Wells, L. S., Journ. Res. Nat. Bur. Standards U.S.A., 1938, vol. 21, p. 617. [M.A. 7-283.]CrossRefGoogle Scholar

page 80 note 3. H. F. McMurdie and E. P. Flint, ibid., 1943, vol. 31, p. 225. [M.A. 9-45.]

page 82 note 1. Mackay, A. L., Acta Cryst., 1952, vol. 5, p. 691 CrossRefGoogle Scholar.

page 84 note 1. Taylor, H. F. W., Journ. Chem. Soc. London, 1953, p. 163 Google Scholar.

page 87 note 1. Heller, L. and Taylor, H. F. W., Journ. Chem. Soc. London, 1951, p.2397. [M.A. 11-471.]Google Scholar

page 88 note 1. Betekhtin, A. G., Mineralogia, Moscow, 1950, p. 877. [M.A. 12-1.]Google Scholar

page 88 note 2. The space-group shows that the layers do not necessarily possess any symmetry, but the fact that they are stacked on top of each other with successive angular displacements of 60° suggests that their essential framework at least approximates to hexagonal symmetry.

page 88 note 3. Brindley, G. W. (editor), X-ray identification and structures of clay minerals, Min. Soc., London, 1951, pp. 72, 311, &c. [M.A. t1-253.]Google Scholar

page 89 note 1. Hendricks, S. B., Amer. Min., 1939, vol. 24, p. 529. [M.A. 7-96.]Google Scholar

page 89 note 2. Bragg, W. L., Guthrie Lecture. Proc. Physical Soc., Sect. B, 1952, vol. 65, p. 833.CrossRefGoogle Scholar

page 90 note 1. Throughout this paper, a-wollastonite denotes pseudo-hexagonal pseudowollastonite α-CaSiO3; β-wollastonite may indicate either triclinic wollastonite or the very similar monoclinic parawollastonite, or an intimate intergrowth of the two.

page 90 note 2. A. Muan and E. F. Osborn, preprint of paper read at the American Iron and Steel Institute, May 1951.

page 90 note 3. Indices on Barnick's, M. unit cell for the monoclinic form; Naturwiss., 1935, vol. 23, p. 770; Strukturber., 1936, vol. 4, p. 207. [M.A. 6-332.]Google Scholar