Chinese Journal of Chromatography ›› 2026, Vol. 44 ›› Issue (10): 1162-1174.DOI: 10.3724/SP.J.1123.2026.01027
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ZHANG Shuang, SUN Mingxia, QIU Hongdeng, CHEN Jia*(
)
Received:2026-01-28
Online:2026-10-08
Published:2026-10-13
Supported by:CLC Number:
ZHANG Shuang, SUN Mingxia, QIU Hongdeng, CHEN Jia. Recent advances in the applications of covalent organic frameworks for strategic critical metal recovery: focusing on rare earths and dispersed metals[J]. Chinese Journal of Chromatography, 2026, 44(10): 1162-1174.
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URL: https://www.chrom-china.com/EN/10.3724/SP.J.1123.2026.01027
Fig. 2 (a) COFs synthesized under green and mild conditions, (b) experimental (blue) and simulated (purple) powder X-ray diffraction (PXRD) patterns of TAPB-BTCA-COF, (c) nitrogen adsorption-desorption isotherms of TAPB-BTCA-COF(The black line is the adsorption curve, and the red line is the desorption curve), (d) histogram of the yield of TAPB-BTCA-COF obtained under different pH values[51]TAPB: 1,3,5-tris(4-aminophenyl)benzene; BTCA: 1,3,5-benzenetricarbaldehyde.
Fig. 4 (a) Schematic diagram of the synthesis of TpPa COFs[40], (b) possible mechanisms of adsorption and separation of REEs by TpPa COFs[40], (c)the influence of concentration on adsorption capacity[40]; (d) schematic diagram of TFPB-DABDA iCOFs for selective recovery of REEs[41], (e) synthesis of sulfonated TFPB-DABDA iCOFs[41], (f) Fourier transform infrared (FT-IR) spectra of TFPB-DABDA iCOFs, TFPB and DABDA[41], (g) changes in O 1s XPS and S 2p spectra of TFPB-DABDA iCOFs before and after adsorption of La3+[41]REEs: rare earth elements; Tp: 1,3,5-triformylphloroglucinol; Pa: p-phenylenediamine; OA: oxalic acid dihydrate; ChCl: choline chloride; TFPB: 1,3,5-tris(p-formylphenyl)benzene; DABDA: 2,5-diaminobenzene-1,4-disulfonic acid.
Fig. 5 (a) Synthetic route of Ugi-COF-DGA, (b) infrared spectra of imine-COF, Ugi-COF, Ugi-COF-NH2, and Ugi-COF-DGA, (c) 13C cross-polarized magic angle rotating solid-state nuclear magnetic resonance spectra of imine-COF, Ugi-COF, Ugi-COF-NH2, and Ugi-COF-DGA, (d) nitrogen adsorption isotherms of imine-COF, Ugi-COF, Ugi-COF-NH2, and Ugi-COF-DGA (the closed circle and the open circle represent the adsorption point and the desorption point respectively)[42]DGA: diglycolic acid.
Fig. 6 (a) Synthetic strategy of COFs-EM[43], (b) effect of initial concentration (COFs-EM 10 mg, 10 mL of germanium-containing solution, 230 r/min, 20 h) [43], (c) reusability performance of COFs-EM[43], (d) influence of pH on the Zeta potential of materials[43]; (e) schematic illustration of the DPDA synthesis process[69], (f) effect of coexisting ions on DPDA adsorption of gallium (Ga(Ⅲ))[69], (g) selectivity coefficient, and (h) cyclic adsorption of DPDA[69]C14H6O8: ellagic acid; C3H6N6: melamine; PG: pyrogallol; DAMN: diaminomaleonitrile; DTB: 2,5-dithiobiurea.
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