RESUMO
The sorption properties of Na-modified Ukrainian Transcarpathian clinoptilolite towards neodymium aqueous solutions under dynamic conditions have been investigated. The sorption capacity of the Na-from of Transcarpathian clinoptilolite towards Nd(III) significantly depends on the concentration of neodymium salt, the pH of the solution, and the heat treatment temperature of the sorbent. Nd(III) is most efficiently sorbed from slightly alkaline solutions (pH 8.5), mainly by adsorption of neutral hydrolyzed forms of Nd(OH)3 on the surface of Na-clinoptilolite samples preheated at 75 °C. During the passage of an Nd(III) solution with a concentration of 1 µg mL-1 through the sorbent at a rate of 3 mL min-1 under optimal conditions, the sorption capacity of Na-clinoptilolite is 7.2 mg g-1, which is in 4 and 2.3 times higher than that of natural and acid-modified forms of this zeolite. It is shown that under the experimental conditions with an increase in the flow rate, the thickness of the stationary surface layer decreases, which leads to a decrease in the sorption capacity of Na-clinoptilolite. The best Nd(III) desorbents are solutions of mineral acids and acidified solutions of alkali metal salts (except NaCl), which provide 93-98 % extraction of lanthanide from the zeolite matrix. The method for neodymium trace amounts preconcentration from aqueous solutions in a solid-phase extraction mode with a further determination of this rare earth element by a spectrophotometric method was developed. The detection limit of this method is 0.75 ng mL-1 and the linearity was evaluated in the range of 2.5-500 ng mL-1.
RESUMO
BACKGROUND: In spite of the fact that terbium is one of the rarest elements in the Earth's crust, it is frequently used for the production of high technological materials. At the result, an effective combination of sample preparation procedure and detection method for terbium ions in different matrices is highly required. The solid-phase extraction procedure with natural Transcarpathian clinoptilolite thermally activated at 350 °C was used to preconcentrate trace amounts of terbium ions in aqueous solutions for a final spectrophotometric determination with arsenazo III. RESULTS: Thermogravimetric investigations confirmed the existence of relations between changes that appeared during dehydratation of calcined zeolite and its sorption affinity. Since the maximum of sorption capacity towards terbium was observed at pH 8.25, a borate buffer medium (2.5 · 10(-4) Ð) was used to maintain ionic force and solution acidity. Terbium was quantitatively removed from the solid-phase extraction column with a 1.0 M solution of sodium chloride (pH 2.5). The linearity of the proposed method was evaluated in the range of 2.5-200 ng · mL(-1) with detection limit 0.75 ng · mL(-1). CONCLUSIONS: Due to acceptable recoveries (93.3-102.0 %) and RSD values (6-7.1) from spiked tap water, the developed method can be successfully applied for the determination of trace amounts of terbium ions in the presence of major components of water. Graphical abstractSorption of terbium(III) ions on clinoptilolite.
