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Surface Areas of Clay Minerals as Derived from Measurements of Glycerol Retention

Published online by Cambridge University Press:  01 January 2024

Sidney Diamond
Affiliation:
Bureau of Public Roads, Physical Research Division, Washington, D.C., USA
Earl B. Kinter
Affiliation:
Bureau of Public Roads, Physical Research Division, Washington, D.C., USA
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Abstract

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The use of glycerol retention measurements to calculate surface areas of clay minerals is described. Assuming that the glycerol retained on external surfaces is monomolecular in thickness, and that both this layer and the monomolecular glycerol layers adsorbed on internal surfaces of montmorillonite, vermiculite, and halloysite are of the density of liquid glycerol, it is calculated that each percentage of glycerol retained corresponds to an area of 17.6 square meters per gram on external surfaces and 35.3 on internal surfaces. The corresponding figures for ethylene glycol retention under these conditions are 22.3 and 44.6, respectively. For nonexpanding clays, surface areas calculated from glycerol retention values agree well with published figures derived from Brunauer, Emmett, and Teller (B.E.T.) gas adsorption measurements. For montmorillonites, surface areas agree reasonably well with published determinations based on B.E.T. treatment using polar adsorbates. Values of surface area are also presented for samples of vermiculite and endellite and for the nonexpanding clay minerals—illite, kaolinite, halloysite, and allophane.

Calculations of the surface area as a function of particle size for montmorillonites of hypothetically uniform particle sizes show that montmorillonites dispersed into very thin flakes must have an appreciable external surface. The ratio of internal to total surface is shown to furnish an estimate of the thickness of the individual montmorillonite flakes. Glycerol retention data for a Wyoming bentonite saturated with a number of different cations are interpreted as indicating particle thicknesses varying from 3 unit cells (about 30A) for Na+ saturation to about 20 unit cells for saturation with a number of polyvalent cations.

Type
Article
Copyright
Copyright © Clay Minerals Society 1956

References

Birrell, K. S., and Gradwell, M., 1956, Ion exchange phenomena in some soils containing amorphous mineral constituents: J. Soil Sci. (London), v. 7, p. 130147.CrossRefGoogle Scholar
Bower, C. A., and Gschwend, F. B., 1952, Ethylene glycol retention of soils as a measure of surface area: Soil Sci. Soc. Amer. Proc., v. 16, p. 342345.CrossRefGoogle Scholar
Brooks, C. S., 1955, Nitrogen adsorption experiments on several clay minerals: Soil Sci., v. 79, p. 331348.CrossRefGoogle Scholar
Brunauer, S., Emmett, P. H., and Teller, E., 1938, Adsorption of gases in multimolecular layers: J. Amer. Chem. Soc., v. 60, p. 309319.CrossRefGoogle Scholar
Dyal, R. S., and Hendricks, S. B., 1950, Total surface of clays in polar liquids as a characteristic index: Soil Sci., v. 69, p. 421432.CrossRefGoogle Scholar
Keenan, A. G., Mooney, R. W., and Wood, L. A., 1951, The relation between exchangeable ions and water adsorption on kaolinite: J. Phys. Coll. Chem., v. 55, p. 14621474.CrossRefGoogle Scholar
Kinter, E. B., and Diamond, S., 1958, Gravimetric determination of monolayer glycerol complexes of clay minerals: in Clays and Clay Minerals, Nat. Acad. Sci.—Nat. Res. Council pub. 566, p. 318333.Google Scholar
Lopez-Gonzalez, J. de D., and Deitz, V. R., 1952, Surface changes in an original and activated bentonite: J. Res. Nat. Bur. Standards, v. 48, p. 325333.CrossRefGoogle Scholar
MacEwan, D. M. C., 1948, Complexes of clays with organic compounds: I. Complex formation between montmorillonite and halloysite and certain organic liquids: Faraday Soc. Trans., v. 44, p. 368375.CrossRefGoogle Scholar
Main, M. S., Kerr, P. F., and Hamilton, P. K., 1950, Occurrence and microscopic examination of reference clay mineral specimens: Amer. Petrol. Inst. Project 49, Rept. 5, Columbia University, N. Y., 59 p.Google Scholar
Mooney, R. W., Keenan, A. G., and Wood, L. A., 1952, Adsorption of water vapor by montmorillonite I: J. Amer. Chem. Soc., v. 74, p. 13671371.CrossRefGoogle Scholar
Mooney, R. W., Keenan, A. G., and Wood, L. A., 1952a, Adsorption of water by montmorillonite II: J. Amer. Chem. Soc., v. 74, 6. 1371-1374.Google Scholar
Mortland, M. M., 1955, Adsorption of ammonia by clays and muck: Soil Sci., v. 80, p. 1118.CrossRefGoogle Scholar
Nelson, R. A., and Hendricks, S. B., 1943, Specific surface of some clay minerals, soils, and soil colloids: Soil Sci., v. 56, p. 285296.CrossRefGoogle Scholar
Orchiston, H. D., 1954, Adsorption of water vapor II: Clays at 25°C.: Soil Sci., v. 78, p. 463480.Google Scholar
Orchiston, H. D., 1955, Adsorption of water vapor III: Homoionic montmorillonites at 25°C.: Soil Sci., v. 79, p. 7178.Google Scholar
Quirk, J. P., 1955, Significance of areas calculated from water vapor sorption isotherms by use of the B.E.T. equation: Soil Sci., v. 80, p. 423430.CrossRefGoogle Scholar
Walker, G. F., 1950, Vermiculite-organic complexes: Nature, v. 166, p. 695697.CrossRefGoogle Scholar
Zettlemoyer, A. C., Young, G. J., and Chessick, J. J., 1955, Studies of the surface chemistry of silicate minerals III: Heats of immersion of bentonite in water: J. Phys. Chem., v. 59, p. 962966.Google Scholar
Zonolite Co., 1954, Chemical and physical properties of vermiculite: Zonolite Co., Chicago, 111., 14 p.Google Scholar