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A Discussion of the Water Content of Vermiculite

Published online by Cambridge University Press:  01 January 2024

W. F. Bradley
Affiliation:
Illinois Geological Survey, Urbana, Illinois, USA
J. M. Serratosa
Affiliation:
Illinois Geological Survey, Urbana, Illinois, USA Institute de Edafologia, CSIC, Madrid, Spain
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Abstract

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Selected chemical and diffraction analyses from the literature, supplemented by thermal and thermogravimetric analyses and infrared absorption observations, are utilized to construct a rational model of the water arrangement in natural vermiculites.

A super cell is arranged by simple modification of the Hendricks water nets to accommodate the somewhat higher water contents, indicated by weight loss analyses, and the exchangeable cations.

A three-cell unit (15.6 × 9 Å) contains two Mg2+·6H2O octahedra centered at the corners and face centers and four 4H2O squares centered about ±5.2 Å along a between the octahedra. The arrangement affords twenty hydrogen bonds near 2.75 Å, twelve between silicate and water layers and eight between water layers, and thirty-two hydrogen bonds near 3.0 Å within water layers. The remaining four hydrogens are not active in the bonding system. The environment of each water molecule is a distorted tetrahedron.

A broad infrared absorption band shows maxima at about 3600, 3450 and 3350 cm−1 at normal incidence, with increased activity in the highest and lowest energies when a flake is tilted. It is concluded that OH axes in the shortest bonds are more inclined to the cleavage planes than are the intermediate length axes.

Type
Article
Copyright
Copyright © Clay Minerals Society 1958

References

Barshad, Isaac, (1948) Vermiculite and its relation to biotite as revealed by base exchange reactions, x-ray analyses, differential thermal curves, and water content: Amer. Min., v. 33, pp. 655678.Google Scholar
Bradley, W. F., Rowland, R. A., Weiss, E. J. and Weaver, C. E. (1958) Temperature stabilities of montmorillonite- and vermiculite-glycol complexes: in Clays and Clay Minerals, Natl. Acad. Sci.—Natl. Res. Council, pub. 566, pp. 348355.Google Scholar
Brindley, G. W. and Youell, R. F. (1953) Ferrous chamosite and ferric chamosite: Min. Mag., v. 30, pp. 5770.Google Scholar
Grudemo, A. (1954) x-Ray examination of the structure of vermiculite: Swedish Cement and Concrete Res. Inst. Proc., no. 22, 56 pp.Google Scholar
Gruner, J. W. (1934) The structures of vermiculites and their collapse by dehydration: Amer. Min., v. 19, pp. 557575.Google Scholar
Hendricks, S. B. and Jefferson, M. E. (1938) Crystal structure of vermiculites and mixed vermiculite-chlorites: Amer. Min., v. 23, pp. 851862.Google Scholar
Mathieson, A. McL. and Walker, G. F. (1954) Crystal structure of magnesium- vermiculite: Amer. Min., v. 39, pp. 231255.Google Scholar
Serratosa, J. M. and Bradley, W. F. (1958) Determination of the orientation of OH bond axes in layer silicates by infrared absorption: J. Phys. Chem., v. 62, pp. 11641167.CrossRefGoogle Scholar
Weaver, C. E. (1958) The effects and geologic significance of potassium “ fixation “ by expandable clay minerals derived from muscovite, biotite, chlorite, and volcanic material: Amer. Min., v. 43, pp. 839861.Google Scholar