School of Municipal and Environmental Engineering, Shandong Jianzhu University, Jinan, 250010, China.
Shandong Electric Power Engineering Consulting Institute Corp., LTD., Jinan, 250010, China.
Environ Sci Pollut Res Int. 2020 Jul;27(19):24531-24541. doi: 10.1007/s11356-020-08794-1. Epub 2020 Apr 19.
Organic micro-pollutants such as pesticides and endocrine disruptors cause serious harm to human health and aquatic ecosystem. In this study, the potential degradation of atrazine (ATZ), triclosan (TCS), and 2,4,6-trichloroanisole (TCA) by UV-activated peroxydisulfate (UV/PDS) and UV-activated HO (UV/HO) processes were evaluated under different conditions. Results showed that UV/PDS process was more effective than UV/HO under the same conditions. Increasing oxidant dosage or decreasing the initial ATZ, TCS, and TCA concentrations promoted the degradation rates of these three compounds. The presence of natural organic matter (NOM) could effectively scavenge sulfate radical (SO•) and hydroxyl radical (HO•) and reduced the removal rates of target compounds. Degradation rates of ATZ and TCA decreased with pH increasing from 5.0 to 9.0 in UV/PDS process, while in UV/HO process, the increase of solution pH had little effect on ATZ and TCA degradation. In the UV/PDS and UV/HO oxidation process, when the solution pH increased from 5 to 8, the removal rates of TCS decreased by 19% and 1%, while when the solution pH increased to 9, the degradation rates of TCS increased by 23% and 17%. CO/HCO had a small inhibitory effect on ATZ and TCA degradation by UV/HO and UV/PDS processes but promoted the degradation of TCS significantly (> 2 mM). Cl had little effect on the degradation of ATZ, TCA, and TCS in UV/HO process. Cl significant inhibited on the degradation of ATZ and TCS, but the influence of Cl on the degradation of TCA was weak in UV/PDS process. Based on these experimental results, the various contributions of those secondary radicals (i.e., carbonate radical, chlorine radical) were discussed. This study can contribute to better understand the reactivities when UV/PDS and UV/HO are applied for the treatment of micro-pollutant-containing waters.
有机微污染物如农药和内分泌干扰物对人类健康和水生生态系统造成严重危害。在这项研究中,评估了在不同条件下,UV 激活过二硫酸盐(UV/PDS)和 UV 激活 HO(UV/HO)过程对莠去津(ATZ)、三氯生(TCS)和 2,4,6-三氯苯甲醚(TCA)的潜在降解作用。结果表明,在相同条件下,UV/PDS 过程比 UV/HO 过程更有效。增加氧化剂剂量或降低初始莠去津、三氯生和 TCA 浓度可以促进这三种化合物的降解速率。天然有机物(NOM)的存在可以有效地清除硫酸根自由基(SO•)和羟基自由基(HO•),从而降低目标化合物的去除率。在 UV/PDS 过程中,随着 pH 值从 5.0 增加到 9.0,莠去津和 TCA 的降解速率降低,而在 UV/HO 过程中,溶液 pH 值的增加对 ATZ 和 TCA 的降解几乎没有影响。在 UV/PDS 和 UV/HO 氧化过程中,当溶液 pH 值从 5 增加到 8 时,TCS 的去除率降低了 19%和 1%,而当溶液 pH 值增加到 9 时,TCS 的降解率分别增加了 23%和 17%。CO/HCO 对 UV/HO 和 UV/PDS 过程中 ATZ 和 TCA 的降解有较小的抑制作用,但显著促进了 TCS 的降解(>2mM)。Cl 对 UV/HO 过程中 ATZ、TCA 和 TCS 的降解几乎没有影响。Cl 对 ATZ 和 TCS 的降解有明显的抑制作用,但对 TCA 的降解影响较弱。基于这些实验结果,讨论了这些次级自由基(即碳酸根自由基、氯自由基)的各种贡献。本研究有助于更好地理解 UV/PDS 和 UV/HO 应用于处理含微污染物水时的反应性。