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Rare earth elements are an important strategic resource, and it is urgent that the rare earth industry continue to explore and develop novel separation methods and technologies. Herein, we fabricated an efficient semi-IPN alginate-clay-poly(n-isopropylacrylamide) (NIPAm) hydrogel by a frozen polymerization method with the help of UV light irradiation, where alginate was employed as the main adsorption functional compound. The as-prepared hydrogel exhibits tough, sponge-like hierarchical macroporous and reversible temperature-responsive characteristics. The maximum adsorption capacity of La3+ is 182 mg/g for the hydrogel composition of 5.0% NIPAm, 4.0% clay, and 3.0% alginate. The Langmuir isotherm fits the data very well, and the adsorption follows the pseudo-second-kinetic equation. The trace of La3+ ions can be effectively separated from the coexisting metal ions. After six repeated adsorption–desorption cycles, no obvious deformation of the shape and or loss of adsorption capacity of the bulk hydrogel ...

Here, we provide an effective method to fabricate magnetic ZnO clay nanocomposite hydrogel via the photopolymerization. The inorganic components endow the hydrogel with high mechanical strength, while the organic copolymers exhibit good adsorption capacity and separation selectivity to La (III) ions. An optimized hydrogel has the maximum compressive stress of 316.60 ± 15.83 kPa, which still exhibits 138.98 ± 7.32 kPa compressive strength after swelling. The maximum adsorption capacity of La ion is 58.8 mg/g. The adsorption matches the pseudo-second-order kinetics model. La (III) ions can be effectively separated from the mixtures of La/Ni, La/Co, La/Cu, and La/Nd in a broad pH range (2.0 to 8.0). After six adsorption–desorption cycles, the hydrogel can maintain its adsorption capacity. This work not only provides a new approach to the synthesis of tough hydrogels under irradiation, but also opens up enormous opportunities to make full use of magnetic nanocomposite hydrogels in environmental fields.