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The influence of layer charge on Zn2+ and Pb2+ sorption by smectites

Published online by Cambridge University Press:  09 July 2018

M. F. Brigatti
Affiliation:
Department of Earth Sciences, University of Modena, Via S. Eufemia 19, 41100-Modena, Italy
G. Campana
Affiliation:
Department of Earth Sciences, University of Modena, Via S. Eufemia 19, 41100-Modena, Italy
L. Medici
Affiliation:
Department of Earth Sciences, University of Modena, Via S. Eufemia 19, 41100-Modena, Italy
L. Poppi
Affiliation:
Department of Earth Sciences, University of Modena, Via S. Eufemia 19, 41100-Modena, Italy

Abstract

Two smectites with different layer charge localization were used to characterize the chemical and structural aspects of minerals treated with 1.9 × 10−2m and 1 m heavy metal solutions (Zn2+ and Pb2+). Natural and treated smectites were analysed by: (1) X-ray powder diffraction first at 25°C and relative humidity of 60% and then at increasing temperature up to 400°C; (2) thermo-gravimetric and differential thermal analysis; (3) X-ray fluorescence; (4) atomic absorption and UV visible spectrophotometries. The sorption of both metals depends on 2:1 layer features and is enhanced when the total layer charge is mostly due to substitution in the octahedral sheet. The variability between Zn2+- and Pb2+-treated smectites in the interlayer water content depends both upon cation electrostatic features and upon smectite layer charge localization. The greatest water content was observed in [Zn2+]1 m-treated smectite showing charge imbalance in the octahedral sheet. In smectites treated with [Zn2+]1 m solutions, an additional thermal reaction occurs at a temperature of ∼380°C, and the d(001) spacing, which is 10 Å at a temperature of ∼200°C, gradually decreases in the temperature range 200–400°C. In smectites treated with 1 m [Pb2+] solutions this value is reached at a temperature of ∼150°C and remains quite constant up to 400°C.

Type
Research Article
Copyright
Copyright © The Mineralogical Society of Great Britain and Ireland 1996

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References

Aronowitz, S., Coyne, L., Lawless, J. & Rishpon, J. (1982) Quantum chemical modelling of smectite clays. Inorg. Chem. 21, 35893593.CrossRefGoogle Scholar
Ben Hadj-Amara, A., Besson, G. & Tchoubar, C. (1987) Caracteristiques structurales d'une smectite dioctahédrique en function de l'ordre-désordre dans la distribution descharges électriques: I Etudes de reflexions 001. Clay Miner. 22, 305318 CrossRefGoogle Scholar
Bergaya, F. & Vayer, M. (1995) Adsorption of a Cu(lI) ethylenediamine complex on clays. Simple method of CEC determination. Euroclay ‘95 Abstracts, 123a-123b.Google Scholar
Del Pennino, U., Mazzega, E., Valeri, S., Alietri, A., Brigatrl, M.F. & Poppi, L., (1981) Interlayer water and swelling properties of monoionic montmorillonites. J. Coll. lnteff. Sci. 84, 301309.CrossRefGoogle Scholar
Komarov, V.S., Roztn, A.T. & Akulicn, N.A. (1977) Sites of the localization of exchange cations of heattreated montmorillonite. Zh. Prikl. Spektrosk. 26, 10991103.Google Scholar
Luca, V. & Cardile, C.M. (1989) Cation migration in smectite minerals: electron spin resonance of exchanged Fe3+-probes. Clays Clay Miner. 37, 325332.CrossRefGoogle Scholar
Pearson, R.G. (1963) Hard and soft acids and bases. J. Am. Chem. Soc. 85, 35333539.CrossRefGoogle Scholar
Pearson, R.G. (1968) Hard and soft acids and bases. HSAB, Part I: Fundamental principles. J. Chem. Educ. 45, 581587.CrossRefGoogle Scholar
Rausell-Colom, J.A., Fernandez, M., Serratosa, J.M., Alcover, J.F. & Gatineau, L. (1980) Organisation de l'espace interlamellaire dans les vermiculites monocouches et anhydres. Clay Miner. 15, 37–58.CrossRefGoogle Scholar
Shannon, R.D. (1976) Revised effective ionic radii and systematic studies of interatomic distances in halides and chalcogenides. Acta Cryst. A32, 751–767.CrossRefGoogle Scholar
Xu, S. & Harsh, J.B. (1992) Alkali-cation selectivity and surface charge of 2:1 clay minerals. Clays Clay Miner. 40, 567574.CrossRefGoogle Scholar