期刊
ENVIRONMENTAL SCIENCE & TECHNOLOGY
卷 52, 期 10, 页码 5600-5609出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.est.8b00481
关键词
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资金
- U.S. National Science Foundation [EAR-1451593]
- Swiss National Science Foundation [200021_149283]
Numerous studies have reported that pollutant reduction rates by ferrous iron (Fe2+) are substantially enhanced in the presence of an iron (oxyhydr)oxide mineral. Developing a thermodynamic framework to explain this phenomenon has been historically difficult due to challenges in quantifying reduction potential (E-H) values for oxide-bound Fe2+ species. Recently, our group demonstrated that E-H values for hematite- and goethitebound Fe(2+)ested if calculated E-H values for oxide-bound Fe2+ could be used to develop a free energy relationship capable of describing variations in reduction rate constants of substituted nitrobenzenes, a class of model pollutants that contain reducible aromatic nitro groups, using data collected here and compiled from the literature. All the data could be described by a single linear relationship between the logarithms of the surface-area normalized rate constant (k(sA)) values and E-H and H-p values [log(k(sA)) = -E-H/0.059 V pH + 3.42]. This framework provides mechanistic insights into how the thermodynamic favorability of electron transfer from oxide-bound Fe2+ relates to redox reaction kinetics.
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