Table 3
Summary of photocatalytic U(VI) based on COF materials
Photocatalysts | Photocatalytic conditions | Bonding mode | Removal rate (%) | Ref |
TpBpy | C0 = 0.12 mM, m/V = 0.5 g·L−1, pH = 7.0, 500 W Xe lamp | vinylene-linked | ~93% in 20 min | [113] |
TTT−DTDA | C0 = 25 ppm, m/V = 1.0 g·L−1, pH = 5.0, 300 W Xe lamp | fused-bithiophene linkers | ~98.2% in 10 h | [114] |
Tp-Tapb | C0 = 0.12 mM, m/V = 1 g·L−1, 350 W Xe lamp | β-keto-enamine | ~92% in 15 min | [19] |
TFPPy-DP | C0 = 0.12 mM, m/V = 0.5 g·L−1, 350 W Xe lamp | amide linkages | ~90% in 20 min | [34] |
LB-COF | C0 = 8 ppm, m/V = 8.0 g·L−1, pH = 5.5, 300 W Xe lamp | imine- and vinyl-linkages | 320 mg·g−1 in 150 min | [115] |
TP-TMT | C0 = 50 ppm, m/V = 1.0 g·L−1, pH = 4.0, 300 W Xe lamp | vinylene-linked | 83% in 240 min | [116] |
Tp-DBD | C0 = 35 ppm, m/V = 0.1 g·L−1, pH = 6.0, 300 W Xe lamp | benzoxazole ring | 10.31 mg·g−1 in 2 h | [117] |
PI-3-AR | C0 = 83 ppm, m/V = 0.17 g·L−1 pH = 4.0, 300 W Xe lamp |
amine-linked | 278 mg·g−1 in 4 h | [118] |
SnS2COF | C0 = 50 ppm, m/V = 0.5 g·L−1, pH = 5.0, 350 W Xe lamp 2 mM HCO3 |
β-ketoenamine, II-type heterojunction | ~95% in 180 min | [36] |
BiOBr@TpPa-1 | C0 = 30 ppm, pH = 6.0, m/V = 0.33 g·L−1, 350 W Xe lamp | β-ketoenamine | ~91% in 540 min | [51] |
TiOCs@COF-TZ | C0 = 8 ppm, m/V = 1 g·L−1, pH = 8.5, 420 nm |
coordinated metal clusters | ~99.86% in 25 min | [120] |
TT-Por COF-Ni | C0 = 50 ppm, m/V = 0.1 g·L−1 pH = 9.0, 350 W Xe lamp |
imine bond | ~97.1% in 360 min | [121] |
Cu-TMT | C0 = 50 ppm, m/V = 0.25 g·L−1 pH = 5.0, 350 W Xe lamp, hole scavenger 0.1 mL |
sp2-c linked | ~98.1% in 360 min | [122] |
NDA-TN-AO | C0 = 10 ppm, m/V = 1 g·L−1 pH = 5.0, 350 W Xe lamp |
vinyl linked | 4.62 mg·g−1 | [124] |
4-Pd-AO | C0 = 10 ppm, m/V = 1 g·L−1 pH = 5.0, 350 W Xe lamp |
β-ketoenamine | 7.36 mg·g−1 in 3 h | [125] |
COF 2-Ru-AO | C0 = 10 ppm, m = 10 mg pH = 5.5, 350 W Xe lamp |
β-ketoenamine | 6.07 mg·g−1 in 27 h | [126] |
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