Green and sustainable separation and recovery of cesium
ion (Cs+) have been an important topic in terms of stable
supply of
this strategic element in recent decades. In this study, to the best
of our knowledge, layered vanadosilicate composite was prepared and
employed for highly selective separation of Cs+ using an
electrochemically controlled process for the first time. The effects
of applied voltage, desorption electrolyte, and ion concentration
in the Cs+ isolation process were thoroughly investigated.
Our results demonstrate that the adsorption and desorption of Cs+ on the electrode can be easily controlled via the redox reactions
of vanadium and the efficiency was significantly improved, exhibiting
the increase in adsorption capacity from 12.7 to 50.3 mg g–1, while the desorption ratio reached 95% in the presence of an electric
field. A good-to-excellent selectivity of Cs+ over K+, Ca2+, and Mg2+ was observed, showing
that the separation factors of Cs+/K+, Cs+/Ca2+, and Cs+/Mg2+ are 11.7,
28.9, and 181.4, respectively. Cyclic test shows that the vanadosilicate-coated
electrode was stable, which indicates that it can be continuously
used to achieve the separation and enrichment of Cs+ in
brines. Raman and X-ray photoelectron spectroscopy results revealed
that the Cs+ adsorption was achieved by coupling ion-exchange
reactions between Cs+ and Na+ and electrochemical
reactions (the redox reaction between V3+ and V4+), and the high adsorption capacity was achieved due to the strong
binding affinity of Cs+ toward oxygen donors. We anticipate
that our findings may point a new way to the green and sustainable
separation and enrichment of Cs+ or other trace strategic
metals from brines using vanadium-based materials in an electrochemically
controlled process.