Hostname: page-component-cd9895bd7-jkksz Total loading time: 0 Render date: 2024-12-28T04:26:48.734Z Has data issue: false hasContentIssue false

Structural Hydroxyls in Sepiolites

Published online by Cambridge University Press:  01 July 2024

J. L. Ahlrichs*
Affiliation:
Consejo Superior de Investigationes Cientificas, Madrid, Spain
C. Serna
Affiliation:
Consejo Superior de Investigationes Cientificas, Madrid, Spain
J. M. Serratosa
Affiliation:
Consejo Superior de Investigationes Cientificas, Madrid, Spain
*
*Visiting scientist from the Department of Agronomy, Purdue University, West Lafayette, Indiana 47907, U.S.A.
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Three sepiolite clays studied showed evidence for the presence of structural hydroxyl groups in three to five different environments depending on the composition of the clay. A 3720 cm−1 i.r. frequency is shown to be characteristic of SiOH at crystal edges which are very abundant in sepiolites. This band has not been seen by most workers because the Nujol, fluorolube or KBr used in sample preparation perturb it sufficiently to obscure it under other OH stretching bands. The 3680 cm−1 band is confirmed as being from the (Mg)3OH and evidence of a very small band near 3640 cm−1 is suggested to arise from limited trioctahedral substitution. The very crystalline Ampandrandava sepiolite shows only the above three bands. The intermediately crystalline Vallecas shows a 3620 cm−1 band in addition which is characteristic of dioctahedral systems and is due to either some vacancy sites or to the presence of attapulgite. This dioctahedral band is greater in the less crystalline Salinelles sepiolite; in addition, it has a smaller 3585 cm−1 band. Mg-Al-vacancy and Mg-Fe‴-vacancy are suggested as the source of the 3620 cm−1 and 3585 cm−1 bands.

Type
Research Article
Copyright
Copyright © 1975, The Clay Minerals Society

References

Cannings, F. R., (1968) An i.r. study of hydroxyl groups on sepiolite J. Phys. Chem. 72 10721074.CrossRefGoogle Scholar
Farmer, V. C. and Russell, J. D., (1964) The i.r. spectra of layer silicates Spectrochim Acta 20 11491173.10.1016/0371-1951(64)80165-XCrossRefGoogle Scholar
Farmer, V. C. Rüssel, J. D. Ahlrichs, J. L. and Velde, B., (1967) Vibrations du groupe hydroxyle dans les silicates en couches Bull. Grpe. Fr. Argiles 19 510.10.3406/argil.1967.1073CrossRefGoogle Scholar
Fernandez Alverez, T., (1972) Activación de la sepiolita con ácido clorhídrico Bol. Soc. Esp. Ceram. Vidrio 11 365374.Google Scholar
Hayashi, H. Otsuka, R. and Imai, N., (1969) I.r. study of sepiolite and palygorskite on heating Am. Miner. 55 16131624.Google Scholar
McDonald, R. S., (1957) Study of the interaction between hydroxyl groups of Aerosil silica and adsorbed nonpolar molecules by i.r. spectrometry J. Am. Chem. Soc. 79 850854.10.1021/ja01561a018CrossRefGoogle Scholar
McDonald, R. S., (1958) Surface functionality of amorphous silica by infrared spectroscopy J. Phys. Chem. 62 11681178.10.1021/j150568a004CrossRefGoogle Scholar
Mendelovici, E., (1973) Infrared study of attapulgite and HCl treated attapulgite Clays and Clay Minerals 21 115119.CrossRefGoogle Scholar
Preisinger, A., (1959) X-ray study of the structure of sepio-lite Clays and Clay Minerals 6 6167.Google Scholar
Prost, R., (1973) Spectre infrarouge de l’eau présente dans láttapulgite et la sépiolite Bull. Grpe. Fr. Argiles 25 5356.10.3406/argil.1973.1178CrossRefGoogle Scholar
Rautureau, M. Tchoubar, C. and Mering, J., (1973) Analyse structurale de la sepiolite a partir de donnees de la diffraction electronique Proc. Int. Clay Conf. 115121.Google Scholar