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The characterization of clay-organic systems

Published online by Cambridge University Press:  09 July 2018

D. T. B. Tennakoon
Affiliation:
Department of Physical Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EP
R. Schlögl
Affiliation:
Department of Physical Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EP
T. Rayment
Affiliation:
Department of Physical Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EP
J. Klinowski
Affiliation:
Department of Physical Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EP

Abstract

The importance of a number of techniques (including 1H and 13C NMR, XRD and IR) in exploring the important catalytic properties of synthetic and natural clays is described. A clear distinction is observed between proven catalytically-active clays (e.g. Al-exchanged) and those which are generally less effective (e.g. Na-exchanged). 13C NMR spectroscopy is used to identify directly products formed within the interlayer regions, and temperature-controlled powder XRD serves as a useful tool for identifying whether or not intercalation occurs under variously defined conditions. High-pressure XRD is used to verify the formation of different products during reaction.

Type
Research Article
Copyright
Copyright © The Mineralogical Society of Great Britain and Ireland 1982

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References

Ballantine, J.A., Davies, M., Purnell, H., Rayanakorn, M., Thomas, J.M. & Williams, K.J. (1981a) J. C. S. Chem. Comm. 427.CrossRefGoogle Scholar
Ballantine, J.A., Purnell, H., Rayanakorn, M., Thomas, J.M. & Williams, K.J. (1981b) J. C. S. Chem. Comm. 8.Google Scholar
Ballantine, J.A., Purnell, H., Rayanakorn, M., Thomas, J.M. & Williams, K.J. (1981c) J. C. S. Chem. Chem. 9.CrossRefGoogle Scholar
Conard, J. (1976) Pp. 8593 in: Magnetic Resonance in Colloid and interface Science (Resing, H. A. & Wade, C. G., editors). American Chemical Society.CrossRefGoogle Scholar
Fyfe, C.A., Thomas, J.M., Klinowski, J. & Gobbi, G.C. (1983) Angew. Chemie 22, 259.Google Scholar
Ŏya, A., Tamegai, F., Sato, M. & Otams, S., (1981) J. Mat. Soc. 16, 263.CrossRefGoogle Scholar
Rayment, T., (1983) J. Appl. Crystallography (in press).Google Scholar
Russell, J.D. & Fraser, A.R., (1971) Clays Clay Miner. 19, 55.Google Scholar
Thomas, J.M. (1982) Pp. 5697 in: Intercalation Chemistry (Whittingham, M. S. & Jacobson, A. J., editors). Academic Press, N.Y.Google Scholar
Yariv, S. & Heller-Kallai, L. (1973) Clays Clay Miner. 21, 199.Google Scholar