The surface free energies of talc and pyrophyllite

The components of the interfacial surface tension of talc and pyrophyllite were determined by measuring the rate of the capillary rise of a number of liquids through thin, sedimented deposits of the powdered minerals. The rate of capillary rise of a liquid in a powder is related to the contact angle between the liquid and the solid by the Washburn equation. The contact angles thus derived were used to determine the apolar (Lifshitzvan der Waals) component, γLW, and the polar, electronacceptor and electron-donor parameters, γ⊕ and γ⊖ respectively, of the Lewis acid/base component of the total interfacial surface energy using the Young equation. The values of γLW for talc and pyrophyllite (31.5 and 34.4 mJ/m2) are slightly smaller than for smectite clay minerals (e.g., the value for hectorite is 39.9 mJ/m2), the electron donor parameter values are roughly comparable for talc and pyrophyllite (γ⊕ = 2.4 and 1.7 mJ/m2) as are the values of the electron acceptor parameter (γ⊖ = 2.7 and 3.2 mJ/m2). The well-known hydrophobicity of these two minerals is due to the remarkably small value (for silicate minerals) of γ⊖(γ⊕ is normally small or zero for silicates and many other oxides). The small values of both γ⊕ and γ⊖ mean that the Lewis acid/base interactions between talc or pyrophyllite and highly polar water molecules are very weak. In contrast, low-charge smectites, the minerals most similar chemically and structurally to talc and pyrophyllite, have much greater values of γ⊖ (≥ 30 mJ/m2) and are hydrophyllic.

[1]  J. Norris,et al.  Surface energies of some smectite clay minerals , 1990 .

[2]  J. Finch,et al.  Critical Surface Tension of Wetting and Flotation Separation of Hydrophobic Solids , 1987 .

[3]  S. Yariv,et al.  Wettability of Clay Minerals , 1990 .

[4]  M. Chaudhury,et al.  Interfacial Lifshitz-van der Waals and polar interactions in macroscopic systems , 1988 .

[5]  E. W. Washburn The Dynamics of Capillary Flow , 1921 .

[6]  C. J. Oss,et al.  Determination of the acid-base characteristics of clay mineral surfaces by contact angle measurements : implications for the adsorption of organic solutes from aqueous media , 1990 .

[7]  F. Fowkes Acid-Base Interactions in Polymer Adhesion , 1981 .

[8]  Frederick M. Fowkes,et al.  ADDITIVITY OF INTERMOLECULAR FORCES AT INTERFACES. I. DETERMINATION OF THE CONTRIBUTION TO SURFACE AND INTERFACIAL TENSIONS OF DISPERSION FORCES IN VARIOUS LIQUIDS1 , 1963 .

[9]  C. J. Oss,et al.  DLVO and Non-DLVO Interactions in Hectorite , 1990 .

[10]  L. Girifalco,et al.  A THEORY FOR ESTIMATION OF SURFACE AND INTERFACIAL ENERGIES. III. ESTIMATION OF SURFACE ENERGIES OF SOLIDS FROM CONTACT ANGLE DATA , 1960 .

[11]  A. J. Murphy,et al.  The Acidity of Clay Minerals in Polymerizations and Related Reactions , 1971 .

[12]  M. Chaudhury,et al.  Determination off the Hydrophobia Interaction Energy-Application to Separation Processes , 1987 .

[13]  I. Brown Bond valences—a simple structural model for inorganic chemistry , 1978 .

[14]  F. E. Bartell,et al.  Wetting Characteristics of Solids of Low Surface Tension such as Talc, Waxes and Resins , 1936 .

[15]  J. Pérez-Rodríguez,et al.  Effects of dry grinding on pyrophyllite , 1988, Clay Minerals.