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Curbing chlorine disinfection byproduct formation with a biomimetic FeTAML oxidation catalyst
被引:1
|作者:
McPherson, James N.
[1
,3
]
Larsen, Freja Troj
[1
]
Lind, Maja Juncher
[1
]
Miller, Christopher J.
[2
]
Waite, T. David
[2
]
McKenzie, Christine J.
[1
]
Lauritsen, Frants R.
[1
]
机构:
[1] Univ Southern Denmark, Dept Phys Chem & Pharm, Campusvej 55, DK-5230 Odense M, Denmark
[2] Univ New South Wales, Water Res Ctr, Sch Civil & Environm Engn, Sydney, NSW 2052, Australia
[3] Tech Univ Denmark, Dept Chem, DK-2800 Lyngby, Denmark
基金:
澳大利亚研究理事会;
关键词:
DRINKING-WATER;
KINETICS;
MECHANISMS;
PHENOLS;
D O I:
10.1039/d3ew00518f
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
We demonstrate, by bench-scale chlorination of local tap water containing phenol (16 mu M, 1.5 ppm) as a model organic micropollutant, that the [Fe(TAML)]- catalyst (TAML = tetra amido macrocyclic ligand) increases the rate of phenol decomposition and suppresses the build-up of chlorophenol disinfection byproducts. Specifically, significantly lower concentrations of trihalomethanes (1.0-2.1 ppb) were formed in the presence of [Fe(TAML)]- compared to those formed in the absence of the catalyst (39-78 ppb). Hydrophobic disinfection byproducts (1-2000 ppb) were monitored in real-time and without any sample preparation using membrane inlet mass spectrometry. This work encourages the incorporation of biomimetic iron catalysts into existing chlorine disinfection processes to harness the oxidative power of chlorine through oxygen- or hydrogen-atom transfer reactions instead of the problematic halogenation reactions which yield disinfection byproducts. An [Fe(TAML)]- catalyst boosts the oxidising power of chlorine disinfectants to clear a model organic pollutant and inhibits formation of trihalomethane disinfection byproducts.
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页码:480 / 489
页数:10
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