The removal of 60Co and 90Sr from the aqueous phase was tested using red mud
- the fine grained residue from bauxite ore processing. This industrial waste
represents a mixture of numerous minerals, mainly oxides and hydroxides of
Fe, Al, Si, and Ti. Experiments were conducted as a function of contact
time, pH, and pollutant concentrations. Kinetic data were well fitted with a
pseudo-second order equation. The calculated rate constants and initial
sorption rates indicated faster sorption of Sr2+ ions. Removal of both
cations rapidly increased with the initial pH increase from 2.5 to 3.5. With
the further increase of pH, Co2+ sorption was nearly constant (98%-100%),
whereas Sr2+ removal remained at the same level to initial pH ~8 and
gradually increased to 100% at pH 12. Equilibrium sorption data followed the
Langmuir model, with the maximum sorption capacities of 0.52 mmol/g for Co2+
and 0.31 mmol/g for Sr2+. Sorbed cations exhibited high stability in
distilled water. Desorption of Co2+ was also negligible in the presence of
the competing Ca2+ cation, while 42%-25% of Sr2+ ions were desorbed depending
on the previously sorbed amount. The results indicate that red mud is of
potential significance as Co2+ and Sr2+ immobilization agent due to its high
efficiency, abundance, and low-cost. [Projekat Ministarstva nauke Republike
Srbije, br. 43009]