JOURNAL OF CHEMICAL ENGINEERING OF JAPAN
Online ISSN : 1881-1299
Print ISSN : 0021-9592
Separation Engineering
Effect of Dopants on Strontium-Adsorption Performance of Metal-Doped Antimony Ion Exchangers
Ayumi Watanabe Yuko KaniMamoru Kamoshida
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2019 年 52 巻 8 号 p. 694-701

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Radioactive strontium-90 (90Sr) is one of the heat-generating nuclides generated by nuclear reactions in reactors, and selective separation of strontium is an efficient treatment method. It was demonstrated that some metal-doped antimony silicates showed high strontium-adsorption performance under acidic condition. The effects of ionic radii and acidity of dopants, namely, tungsten, vanadium, tantalum, and zirconium, on the strontium-adsorption performance of antimony silicates under acidic condition and a solution containing sodium ions were investigated. The results of the investigation revealed that the ion-exchange capacity of metal-doped antimony silicate was 2.4 mEq/g for vanadium, 1.8 mEq/g for tungsten and tantalum, and 1.3 mEq/g for zirconium; basically, it decreased as a function of the ionic radius of the dopant. The tungsten-, vanadium-, and tantalum-doped antimony silicates had high distribution coefficients for strontium (KdSr) of over 103 L/kg in deionized water, chloride solution, and nitric acid solution under various pH conditions. KdSr under acidic condition increased with increasing acidity of the dopants. At various sodium concentrations, KdSr of tungsten-, vanadium-, and tantalum-doped antimony silicates was greater than KdCa. The selectivity coefficient of strontium over sodium (KSr–Na) was found to depend on the ionic radius of the dopant. These results indicate that the ionic radii and acidity of the dopants affect the total number of adsorption sites and activation of individual adsorption sites; that is, larger ionic radii of dopants cause collapse of the pyrochlore structure of the antimony silicates, thereby decreasing the ion-exchange capacity, and dopants with high acidity support the formation of cationic-exchange groups that increase KdSr for antimony silicates under acidic conditions.

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© 2019 The Society of Chemical Engineers, Japan
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