过氧乙酸
激进的
钴
化学
腐植酸
碳酸氢盐
反应速率常数
降级(电信)
有机化学
羟基自由基
无机化学
光化学
核化学
过氧化氢
动力学
物理
电信
肥料
量子力学
计算机科学
作者
Juhee Kim,Penghui Du,Wen Liu,Cong Luo,He Zhao,Ching‐Hua Huang
标识
DOI:10.1021/acs.est.0c00356
摘要
Peracetic acid (PAA) is increasingly used as an alternative disinfectant and its advanced oxidation processes (AOPs) could be useful for pollutant degradation. Co(II) or Co(III) can activate PAA to produce acetyloxyl (CH3C(O)O•) and acetylperoxyl (CH3C(O)OO•) radicals with little •OH radical formation, and Co(II)/Co(III) is cycled. For the first time, this study determined the reaction rates of PAA with Co(II) (kPAA,Co(II) = 1.70 × 101 to 6.67 × 102 M-1·s-1) and Co(III) (kPAA,Co(III) = 3.91 × 100 to 4.57 × 102 M-1·s-1) ions over the initial pH 3.0-8.2 and evaluated 30 different aromatic organic compounds for degradation by Co/PAA. In-depth investigation confirmed that CH3C(O)OO• is the key reactive species under Co/PAA for compound degradation. Assessing the structure-activity relationship between compounds' molecular descriptors and pseudo-first-order degradation rate constants (k'PAA• in s-1) by Co/PAA showed the number of ring atoms, EHOMO, softness, and ionization potential to be the most influential, strongly suggesting the electron transfer mechanism from aromatic compounds to the acetylperoxyl radical. The radical production and compound degradation in Co/PAA are most efficient in the intermediate pH range and can be influenced by water matrix constituents of bicarbonate, phosphate, and humic acids. These results significantly improve the knowledge regarding the acetylperoxyl radical from PAA and will be useful for further development and applications of PAA-based AOPs.
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