School of Environment and Energy, South China University of Technology, Guangzhou 510006, China.
South China Institute of Environmental Sciences, Ministry of Ecology and Environment, Guangzhou 510655, China.
Sci Total Environ. 2022 Feb 25;809:152185. doi: 10.1016/j.scitotenv.2021.152185. Epub 2021 Dec 7.
Organophosphorus esters (OPEs), one kind of the emerging contaminants with high frequency of detection, is rather refractory in natural environment, thus posing great threat to human health. This study investigated the feasibility and mechanism of tris(2-chloroethyl) phosphate (TCEP) degradation in thermally activated persulfate (TAP) system. Influence of impact factors, such as PDS dosage, temperature, initial pH, and presence of natural water matrix (Cl, NO, HPO, NH, humic acid), were evaluated. Results showed that 100% degradation of TCEP can be achieved in TAP system in 40 min at 60 °C. SO as the dominant oxidant for TCEP degradation was proved by quenching experiment and verified by EPR analysis. Alkaline condition exerted great inhibitory effect by affecting the constituents of oxidative radicals. It is suggested that Cl and HPO at lower dosages promoted the degradation by stimulating ·OH production and forming oxidative radicals with better selectivity. Intermediates identified by high resolution mass spectrometer was suggested less toxic than TCEP by ECOSAR program. Meanwhile, the illustrated oxidation mechanism mainly involved radical attack at CCl bond and cleavage of CO bond, as further confirmed by frontier electron density calculation and wavefunction analysis. Moreover, cyclic degradation of TCEP indicated the constant release of SO in 450 min, suggesting high efficiency and stability of PDS in TAP system. Four selected OPEs achieved complete removal in TAP system and their degradation discrepancy was further discussed based on the distinctive structures. Altogether, TAP technology can be used as an efficient method in TCEP removal with great potential for application.
有机磷酯 (OPEs) 是一种新兴污染物,检出频率较高,在自然环境中相当难降解,因此对人类健康构成了巨大威胁。本研究考察了三( 2-氯乙基)磷酸酯(TCEP)在热活化过硫酸盐(TAP)体系中降解的可行性和机制。评估了影响因素,如过一硫酸盐(PDS)剂量、温度、初始 pH 值以及天然水基质(Cl、NO、HPO、NH、腐殖酸)的存在的影响。结果表明,在 60°C 下,TAP 体系中 100%的 TCEP 在 40 min 内完全降解。通过淬灭实验和 EPR 分析证明,SO是 TCEP 降解的主要氧化剂。碱性条件通过影响氧化自由基的组成对 TCEP 的降解产生了很大的抑制作用。Cl 和 HPO在较低剂量下通过刺激·OH 的产生和形成选择性更好的氧化自由基,促进了 TCEP 的降解。高分辨率质谱仪鉴定的中间产物通过 ECOSAR 程序被建议比 TCEP 毒性更小。同时,所提出的氧化机制主要涉及 CCl 键的自由基攻击和 CO 键的断裂,这进一步通过前沿电子密度计算和波函数分析得到证实。此外,TCEP 的循环降解表明在 450 min 内 SO 的持续释放,表明 PDS 在 TAP 体系中的效率和稳定性高。四种选定的 OPEs 在 TAP 体系中完全去除,并根据其独特的结构进一步讨论了它们的降解差异。总之,TAP 技术可以作为一种高效去除 TCEP 的方法,具有很大的应用潜力。