Here, we discuss the fabrication and problems of application of chitosan-based composite materials for the removal of hazardous metal ions from tap water and wastewater. The chitosan-based composites containing iron oxides for the uptake of Sr2+ ions were fabricated via a co-precipitation method with variation of the iron/chitosan ratio and pH of the medium. The morphology and composition of the fabricated sorbents were characterized using scanning electron microscopy–energy dispersive X-ray spectroscopy (SEM–EDX) and X-ray diffraction (XRD) analysis. We have shown that the suggested fabrication approach allows for a homogeneous distribution of the inorganic phase in the polymer matrix. Investigations of the sorption performance of the composites have shown that they are efficient sorbents for 90Sr radionuclides uptake from tap water. The composite sorbent containing amorphous iron oxide in a chitosan matrix and calcined at 105 °C showed the best sorption characteristics. We have also demonstrated that there is an optimal iron oxide content in the composite: with increasing oxide content, the efficiency of the sorbents decreases due to poor stability in solution, especially in alkaline media. The alternative approach yielding magnetic chitosan-based composites with sufficiently good sorption performance and stability in neutral and weakly alkaline media is suggested.
The efficiency of the removal of Cs-137 radionuclides with porous and non-porous resorcinol–formaldehyde resins from alkaline solutions simulating the composition of real liquid radioactive waste (LRW) streams has been evaluated. Resins were synthesized through the polycondensation of resorcinol and formaldehyde in an alkaline medium at a molar ratio of 1.8/2.2 and a temperature of 210 °C. The Cs-137 distribution coefficients on RFRs in alkaline solutions simulating LRW were above 103 mL/g under static sorption conditions. In a model solution with pH 11, the full dynamic sorption capacity of non-porous RFR was 0.178 mmol/g. The values of the full dynamic sorption capacities of porous RFRs were 0.274 and 1.035 mmol/g for resins obtained with calcium carbonate and toluene as templates, respectively. When the sizes of RFR beads increased two-fold, the volume until 5% cesium breakthrough decreased by 20–40%. The most pronounced beneficial effect of the RFR’s porosity was observed at flow rates from 25 to 50 BV/h. It was shown that the negative effect of metal cations on Cs-137 uptake increases in the following order: Na+ < Mg2+ < Ca2+ < K+. The number of bed volumes of LRW-simulating solution decontaminated with RFRs until 5% cesium breakthrough was above 450; that is higher than the value of known commercially available analogs. The latter shows that the developed RFRs are promising for application in technological schemes of alkaline LRW processing.
An organomineral sorbent based on mixed nickel-potassium ferrocyanide and chitosan to be used in removal of Cs-137 radionuclide from highly mineralized media with high pH has been fabricated. The synthesized sorbent was applied to remove Cs-137 from model solutions under static and dynamic conditions. The effects of contact time, pH, and presence of sodium ions and complexing agents in the process of Cs-137 removal have been investigated. The sorbent is distinguished by increased stability to the impact of alkaline media containing complexing agents, whereas the sorbent capacity in solutions with pH 11 exceeds 1000 bed volumes with the Cs-137 removal efficiency higher than 95%.
21 April 2017 in Separation Science and Technology
Chitosan-ferrocyanide sorbents (CFS) based on ferrocyanides Ni-K, Cu-K and Zn-K for concentrating Cs-137 from the seawater have been obtained. Sorbent CFS Zn-K can be used in sorption-regeneration cycle using 5 M solution of NH4NO3 as the eluent. In dynamic condition, the sorption efficiency of Cs-137 and the elution for the CFS Zn-K exceeds 95%. The two-staged scheme of Cs-137 concentrating from seawater is suggested. First stage is the removal of radionuclide from seawater by the CFS Zn-K sorbent, and the second stage is the sorption of Cs-137 from eluate by the CFS Ni-K sorbent.