1. Enhanced degradation of trichloroethylene using bentonite-supported nanoscale Fe/Ni and humic acids
- Author
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Jiawei Chen, Xi Cao, Dan Zhao, Yitong Han, Shihe Wang, and Dezhong Yang
- Subjects
chemistry.chemical_classification ,Trichloroethylene ,Inorganic chemistry ,02 engineering and technology ,010501 environmental sciences ,021001 nanoscience & nanotechnology ,01 natural sciences ,Catalysis ,Reaction rate ,chemistry.chemical_compound ,Reaction rate constant ,chemistry ,Reagent ,Bentonite ,Environmental Chemistry ,Humic acid ,Reactivity (chemistry) ,0210 nano-technology ,0105 earth and related environmental sciences - Abstract
Nanoscale zero-valent iron, named nano-Fe0, is a reagent used to degrade trichloroethylene in groundwater. However, the efficiency of nano-Fe0 is moderate due to issues of dispersion and reactivity. As an alternative we synthesized bentonite-supported nanoscale Fe/Ni bimetals, named bentonite-Fe/Ni, to test the degradation of trichloroethylene in the presence of Suwannee River humic acids, as a representative of natural organic matter. 0.1 mmol/L trichloroethylene was reacted with 0.5 g/L of nano-Fe0, bentonite-Fe, Fe/Ni, and bentonite-Fe/Ni nanoparticles. Results show first that without humic acids the reaction rate constants k obs were 0.0036/h for nano-Fe0, 0.0101/h for bentonite-Fe, 0.0984/h for Fe/Ni, and 0.181/h for bentonite-Fe/Ni. These findings show that bentonite-Fe/Ni is the most efficient reagent. Second, the addition of humic acids increased the rate constant from 0.178/h for 10 mg/L humic acids to 0.652/h for 40 mg/L humic acids, using the bentonite-Fe/Ni catalyst. This finding is explained by accelerated dechlorination by faster electron transfer induced by humic quinone moieties. Indeed, the use of 9, 10-anthraquinone-2, 6-disulfonate as a humic analogue gave similar results.
- Published
- 2016
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