Autonomous enrichment and deep removal of heavy metals by salt-tolerant gradient polyelectrolyte hydrogels

Abstract

The integration of nanostructured materials into hydrogel matrix with chemical gradient holds great promise in gathering the pollutants and enhancing their adsorption or photocatalytic performance. However, the electric potentials rooting in the common gradient polyelectrolyte hydrogel are almost completely shielded by the co-existing counter-ions. In this study, a salt-tolerant gradient polycationic electrolyte hydrogel was fabricated by free radical copolymerization under the induction of unilateral UV illumination, which was used as nanofillers matrix. The cation-π interactions between the adjacent cations and aromatic rings endow the gradient polycationic electrolyte hydrogels deserving the salt-tolerant properties. Thus, the build-in electric potentials are still reactive on enrichment of the anionic heavy metals in highly concentrated salt solutions, altering the defects of the common gradient polyelectrolyte hydrogel. Using Sb(V) adsorption and Cr(VI) photocatalytic reduction as target reactions, the gradient composite hydrogels always display fast and high removal capacities towards these anionic pollutants in the saline solutions of 500 mM, as well as good stability and reusability. This salt-tolerant hydrogel matrix provides a smart material platform with self-driven forces in the fields of pollutant enrichment and removal.