Constructed a charge transfer complex for efficient uranium separation, indicating high specificity against lanthanides.
Selective detection and efficient separation of uranium from lanthanides (Ln) is very important but currently remains a great challenge considering the chemical similarities between uranium and Ln. Herein, a charge transfer complex (CTC) (TPP-TCNQ CTC) was constructed by introducing triphenylphosphine (TPP) as the donor and 7,7,8,8-tetracyanoquinodimethane (TCNQ) as the receptor. The optical properties of TPP-TCNQ CTC, including absorption, fluorescence, and light scattering (LS), simultaneously exhibit distinct evolution upon the specific interaction with UO22+, facilitating its sensitive and selective detection with the limit of detection (LOD) down to 6.7 nM for the LS method. More importantly, TPP-TCNQ CTC can coordinate with UO22+ to form coprecipitation in a wide pH range (1.0–9.0) with fast kinetics (1 min) and high specificity (KdU, 3.48 × 104 mL g–1), achieving the efficient precipitation separation of UO22+ (>90%) without complex procedures. The specific coprecipitation of UO22+ over other Ln favors highly selective detection and ultraefficient separation of UO22+ and endows the TPP-TCNQ CTC with great potential in rare earth tailings treatment. This work offers a new strategy for charge transfer complex (CTC) construction and a promising platform for the detection and separation of radioactive nuclides.
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Fan et al. (2025) studied this question.
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