期刊
ENVIRONMENTAL SCIENCE & TECHNOLOGY
卷 51, 期 4, 页码 2355-2365出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.est.6b05513
关键词
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资金
- National Science Foundation [CBET-1159764, CBET-1453081]
- Div Of Chem, Bioeng, Env, & Transp Sys
- Directorate For Engineering [1453081] Funding Source: National Science Foundation
The detection of hydroxyl radicals (OH center dot) is typically accomplished by using reactive probe molecules, but prior studies have not thoroughly investigated the suitability of these probes for use in electrochemical advanced oxidation processes (EAOPs), due to the neglect of alternative reaction mechanisms. In this study, we investigated the suitability of four OH center dot probes (coumarin, p-chlorobenzoic acid, terephthalic acid, and p-benzoquinone) for use in EAOPs. Experimental results indicated that both coumarin and p-chlorobenzoic acid are oxidized via direct electron transfer reactions, while p-benzoquinone and terephthalic acid are not. Coumarin oxidation to form the OH center dot adduct product 7-hydroxycoumarin was found at anodic potentials lower than that necessary for OH center dot formation. Density functional theory (DFT) simulations found a thermodynamically favorable and non-OH center dot mediated pathway for 7-hydroxycoumarin formation, which is activationless at anodic potentials > 2.10 V/SHE. DFT simulations also provided estimates of E degrees values for a series of OH center dot probe compounds, which agreed with voltammetry results. Results from this study indicated that terephthalic acid is the most appropriate OH center dot probe compound for the characterization of electrochemical and catalytic systems.
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