所属专题: 金属有机框架材料
• 综述 •
衣晓虹, 王崇臣. 铁基金属-有机骨架及其复合物高级氧化降解水中新兴有机污染物[J]. 化学进展, 2021, 33(3): 471-489.
Xiaohong Yi, Chongchen Wang. Elimination of Emerging Organic Contaminants in Wastewater by Advanced Oxidation Process Over Iron-Based MOFs and Their Composites[J]. Progress in Chemistry, 2021, 33(3): 471-489.
新兴有机污染物(Emerging organic contaminants,EOCs)是对人体健康及生态环境具有潜在或实质威胁的新型化学污染物。由于其被频繁使用且能在水生生态系统中持久性存在而对水生生物健康和安全造成严重威胁,故引起大众越来越多的关注。以活性污泥法为代表的传统水处理工艺通常不足以消除这些新兴有机污染物。为高效去除新兴有机污染物,基于新材料的高级氧化技术是最主要的深度处理技术之一。铁基金属-有机骨架(Fe-MOFs)及其复合物在诸多领域得到了广泛的应用,特别是在催化氧化去除水中有机污染物方面展现出良好的应用前景。通过合成方法改进、合成后改性以及与特定功能材料复合等方法可有效提升Fe-MOFs及其相关材料的吸附性能、增强其光吸收特性和促进载流子有效分离等。本文重点综述了Fe-MOFs及其复合物高级氧化(光催化、类芬顿和硫酸根自由基($SO_{4}^{-·}$)介导的氧化)去除水中新兴有机污染物的研究进展,并探讨了未来研究所面临的机遇和挑战。
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Catalysts/Dosage (g·L-1) | Target Pollutants/Volume (mL)/concentration (mg·L-1)/pH | Light Source | Reaction Time (min) | Degradation Efficiency (%) | ref |
---|---|---|---|---|---|
Photocatalytic oxidation | |||||
WO3/MIL-53(Fe)/0.2 | 2,4-dichlorophenoxyacetic acid/100/45/2.5 | sun light | 240 | ~100 | |
CdS/MIL-53(Fe)/0.75 | ketorolac tromethamine/100/10/6 | 85 W Oreva CFL bulb(λ≥ 420 nm) | 330 | 80 | |
MIL-88A/g-C3N4/1.0 | tetracycline/100/10/NA | 1000 W iodine tungsten lamp(λ≥ 420 m) | 120 | 22 | |
Ag/AgCl@MIL-88A(Fe)/0.4 | ibuprofen/50/10/NA | 500 W Xe lamp(λ≥ 420 nm) | 210 | 100 | |
BiOI/MIL-88B(Fe)/0.3 | ciprofloxacin/100/10/NA | 150 W Xe lamp(AM 1.5G) | 270 | 80 | |
MIL-100(Fe)/PANI/0.25 | tetracycline/200/10/NA | 300 W Xe lamp | 120 | 84 | |
Fenton-like reaction | |||||
1T-MoS2@MIL-53(Fe)+20 mmol/L·H2O2/0.4 | ibuprofen/50/10/7.0 | 500 W Xe lamp(λ≥ 420 nm) | 120 | 100 | |
g-C3N4/PDI@NH2-MIL-53(Fe)+10 mmol/L·H2O2/0.4 | tetracycline/50/50/6.0 | 5 W LED white lamp(380~800 nm) | 40 | 90 | |
g-C3N4/PDI@NH2-MIL-53(Fe)+10 mmol/L·H2O2/0.4 | carbamazepine/50/50/6.0 | 5 W LED white lamp(380~800 nm) | 150 | 78 | |
g-C3N4/PDI@NH2-MIL-53(Fe)+10 mmol/L·H2O2/0.4 | bisphenol A/50/50/6.0 | 5 W LED white lamp(380~800 nm) | 10 | 100 | |
g-C3N4/PDI@NH2-MIL-53(Fe)+10 mmol/L·H2O2/0.2 | bisphenol A/50/2/6.0 | 5 W LED white lamp(380~800 nm) | 10 | 100 | |
MIL-88A(Fe)+100 μL H 2O2/0.2 | bisphenol A/50/10/NA | 350 mW LED visible light | 60 | ~100 | |
PANI/MIL-88A(Fe)+20 μL H 2O2/0.2 | bisphenol A/50/10/5.1 | 5 W LED visible light | 30 | 100 | |
CUS-MIL-100(Fe)+6 mmol/L H2O2/0.5 | sulfamethazine/80/20/3.0 | in dark | 60 | 100 | |
Pd@MIL-100(Fe)+40 μL H 2O2/0.125 | theophylline/40/20/4.0 | 300 W Xe lamp(λ≥ 420 nm) | 150 | 99.5 | |
Pd@MIL-100(Fe)+40 μL H 2O2/0.125 | ibuprofen /40/20/4.0 | 300 W Xe lamp(λ≥ 420 nm) | 150 | 100 | |
Pd@MIL-100(Fe)+40 μL H 2O2/0.125 | bisphenol A/40/20/4.0 | 300 W Xe lamp(λ≥ 420 nm) | 150 | 68 | |
Pd-PTA-MIL-100(Fe)+40 μL H 2O2/0.125 | theophylline/40/20/4.0 | 300 W Xe lamp(λ≥ 420 nm) | 150 | 99.5 | |
Pd-PTA-MIL-100(Fe)+40 μL H 2O2/0.125 | ibuprofen/40/20/4.0 | 300 W Xe lamp(λ≥ 420 nm) | 180 | 99.5 |
Catalysts/Dosage (g·L-1) | Target Pollutants/Volume (mL)/concentration (mg·L-1)/pH | Light Source | Reaction Time (min) | Degradation Efficiency (%) | ref |
---|---|---|---|---|---|
WO3/MIL-100(Fe)+40 μL H 2O2/0.25 | bisphenol A/80/10/3.0 | 25 W LED visible light | 20 | 100 | |
MIL-100(Fe)/g-C3N4+50 μL H 2O2/0.5 | diclofenac sodium/200/0.1 mmol/L/NA | 300 W Xe lamp | 50 | 100 | |
MIL-100(Fe)/Fe-SPC+40 mmol/L·H2O2/1.0 | thiamethoxam/50/60/7.5 | 600 W ultrasonic probe | 100 | 100 | |
Cu2O/MIL-100(Fe/Cu)+49 mmol/L H2O2/0.5 | thiacloprid/50/80/7.47 | 500 W Xe lamp | 25 | 90 | |
MIL-100(Fe)/TiO2+20 μL H 2O2/0.05 | tetracycline /100/100/NA | 450 W Xe arc lamp | 60 | 85.8 | |
MIL-100(Fe)@Fe3O4/CA+H2O2/0.2 | tetracycline /50/10/5.0 | 150 W Xe lamp(λ≥ 400 nm) | 210 | 85 | |
M.MIL-100(Fe)@ZnO +10 mmol/L·H2O2/0.2 | bisphenol A/50/5/2.0 | LSH-500 W Xe arc lamp | 60 | ~100 | |
M.MIL-100(Fe)@ZnO +10 mmol/L·H2O2/0.2 | atrazine/50/5/2.0 | LSH-500 W Xe arc lamp | 120 | >80 | |
Oxidation of activated persulfate | |||||
AgIO3/MIL-53(Fe)+50 mg·L-1 PS/0.5 | methyl malathion/100/20/5.0 | sun light | 120 | 93 | |
AgIO3/MIL-53(Fe)+50 mg·L-1 PS/0.5 | chlorpyrifos/100/20/5.0 | sun light | 120 | 97 | |
AgIO3/MIL-53(Fe)+50 mg·L-1 PS/0.5 | methyl malathion(binary mixture)/100/20/5.0 | sun light | 180 | 100 | |
AgIO3/MIL-53(Fe)+50 mg·L-1 PS/0.5 | chlorpyrifos(binary mixture)/100/20/5.0 | sun light | 180 | 50 | |
MIL-88A@MIP+10.8 mmol/L PS/0.5 | dibutyl phthalate/100/3.5/ not adjusted | in dark | 480 | 77.4 | |
MIL-88A@MIP+10.8 mmol/L PS/0.5 | dibutyl phthalate/100/4.0/ not adjusted | in dark | 480 | >80.4 | |
MIL-88A@MIP+10.8 mmol/L PS/0.5 | dibutyl phthalate/100/5.0/ not adjusted | in dark | 480 | 80.4 | |
MIL-88B(Fe)+2 mmol/L PS/0.6 | bisphenol A/100/10/6.5~7.2 | 300 W Xe lamp(λ≥ 420 nm) | 25 | 100 | |
Bi12O17Cl2/MIL-100(Fe)+0.2 mmol/L PS/0.25 | bisphenol A/200/10/5.2 | 300 W Xe lamp | 40 | 100 | |
g-C3N4/MIL-101(Fe)+1 mmol/L PS/0.5 | bisphenol A/NA/10/NA | 300 W Xe lamp(λ≥ 400 nm) | 60 | 98 | |
AQS-NH-MIL-101(Fe)+10 mmol/L PS/0.2 | bisphenol A/25/60/5.76 | in dark | 120 | 97.7 |
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