Author： Voronina A. Semenishchev V. Nogovitsyna E. Betenekov N.
Publisher： Springer Publishing Company
ISSN： 0236-5731
Source： Journal of Radioanalytical and Nuclear Chemistry, Vol.298, Iss.1, 2013-10, pp. : 67-75
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Abstract
Sorption isotherm of caesium from tap water by mixed nickel–potassium ferrocyanide based on hydrated titanium dioxide is obtained for a wide range of concentrations of caesium. It is shown that there are three types of specificity to caesium sorption sites in this sorbent. Sorption chemisms of caesium are studied, factors conditioned high sorption capacity of the sorbent are revealed. It is shown that occupation of sorption sites I and II is well approximated by Langmuir equilibrium and this process can be described within the bounds of theory of ion exchange. The expected sorption chemism of caesium by sorption sites III at high concentrations of caesium (>50 mg L−1) is precipitation of mixed nickel–caesium ferrocyanide in pore space of the sorbent.
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