The adsorption of hafnium species on glass was found to increase with the solution pH and hafnium concentration. The effects on the adsorption of the solution preparation and age were studied and the equilibration time for the adsorption process was determined. The surface area of the glass sample was determined by the B.E.T. method using water vapor. The results are discussed in terms of the hydrolyzed hafnium(IV) species. At equilibrium, nearly monolayer coverage was obtained at pH > 4.5. Under these conditions hafnium is in the solution in its entirety in the form of neutral, soluble Hf(OH)4 species. In the close packed adsorption layer the cross-sectional area of this species is 24 A. 2 which is nearly the same as for water on silica surfaces. T^Tumerous experiments dealing with the adsorption of metal ions on glass from aqueous solutions have been reported in the literature. These studies dealt, for example, with sodium (6,11,18), potassium (6), cesium (11, 18), thallium(I) and thallium(III) (32), silver (II), cal cium (6), zirconium (29, 34, 36), ruthenium (4, 31), cerium (4), promethium (4), gold (26), bismuth (17), lead (17), polonium (17, 28, 33), thorium (24), radium (22), protactinium (35), uranium (30), and plutonium (7, 8, 9, 10,13, 14). In the majority of the experiments radio active isotopes were used in tracer quantities. It was established without exception that the pH was the most important parameter affecting the adsorption. In the case of simple non-hydrolyzable ions the pH effects were interpreted in terms of the hydrolysis of the glass surface. It is also generally suggested that the mechanism of adsorption of non-hydrolyzed ions is essentially an ion exchange of the adsorbate species with the cations in the glass (3), although there are numerous observations which 44 Downloaded by MICHIGAN STATE UNIV on February 18, 2015 |