The kinetics of caesium sorption by potassium copper ferrocyanide have been studied. Liquid film diffusion is rate controlling in very dilute solutions of caesium (3.8 × 10 −6 m). The average film diffusion coefficient was found to be 1.465 × 10 −9 m 2 s −1 at 20°C and the activation energy for the corresponding process was found to be 15.14 kJ mol −1 . Chemical reaction rate controls the caesium‐potassium ion exchange process at a higher caesium concentration of 3.8 × 10 −3 m. The shell progressive reaction model was found applicable to the sorption process. The activation energy for the caesium‐potassium ion exchange reaction was measured to be 74.85 kJ mol −1 . Finally, a comparison between the theoretical and the experimental sorption profile has been made to demonstrate the validity of the theory.
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Lee et al. (1983) studied this question.
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