Research Center for Eco-Environmental Sciences (RCEES), Chinese Academy of Sciences, Beijing 100085, China.
Environ Sci Technol. 2023 Aug 22;57(33):12523-12533. doi: 10.1021/acs.est.3c04134. Epub 2023 Aug 8.
Trace Cu(II), which inherently exists in soil and some water/wastewater, can trigger persulfate oxidation of some pollutants, but the oxidation capability and mechanism are not well understood, especially toward refractory pollutants. We report in this research that benzothiazole (BTH), a universal refractory pollutant typically originating from tire leachates and various industrial wastewater, can be facilely and selectively removed by peroxydisulfate (PDS) with an equimolar BTH/PDS stoichiometry in the presence of environmental-relevant contents of Cu(II) (below several micromoles). Comprehensive scavenging tests, electron spin resonance analysis, spectroscopy characterization, and electrochemical analysis, revealed that PDS first reduces the BTH-coordinated Cu(II) to Cu(I) and then oxidizes Cu(I) to high-valent Cu(III), which accounts for the BTH degradation. Moreover, once the reaction is initiated, the superoxide radical is probably produced in the presence of dissolved oxygen, which subsequently dominates the reduction of Cu(II) to Cu(I). This facile oxidation process is also effective in removing a series of BTH derivatives (BTHs) that are of environmental concern, thus can be used for their source control. The results highlight the sequential Cu(II)-Cu(I)-Cu(III) transition during PDS activation and the crucial role of contaminant coordination with Cu(II) in oxidative transformation.
痕量的铜(Cu(II))普遍存在于土壤和部分水/废水中,它能引发过硫酸盐对一些污染物的氧化,但目前人们对其氧化能力和机制的了解还很有限,特别是针对难处理的污染物。在本研究中,我们报告称,苯并噻唑(BTH)作为一种普遍存在的难处理污染物,通常源自轮胎浸出物和各种工业废水中,在环境相关浓度的 Cu(II)(低于几个微摩尔)存在下,BTH 与过二硫酸盐(PDS)以化学计量比 1:1 反应,可以很容易且有选择性地被去除。综合的清除实验、电子顺磁共振分析、光谱学特性分析和电化学分析表明,PDS 首先将 BTH 配位的 Cu(II)还原为 Cu(I),然后将 Cu(I)氧化为高价态的 Cu(III),从而导致 BTH 的降解。此外,一旦反应开始,超氧自由基可能会在溶解氧的存在下产生,随后主导 Cu(II)还原为 Cu(I)。这个简单的氧化过程对于一系列具有环境关注的 BTH 衍生物(BTHs)的去除也同样有效,因此可用于它们的源头控制。该结果强调了在 PDS 激活过程中 Cu(II)-Cu(I)-Cu(III)的连续转变,以及污染物与 Cu(II)配位在氧化转化中的关键作用。