TCEP
过硫酸盐
化学
黄铁矿
磷酸盐
降级(电信)
激进的
特里斯
水溶液
无机化学
核化学
有机化学
催化作用
矿物学
生物化学
磷化氢
电信
计算机科学
作者
Wenjie Lian,Xiaoyun Yi,Kaibo Huang,Ting Tang,Rong Wang,Xueqin Tao,Zeli Zheng,Zhi Dang,Guining Lu,Guining Lu
标识
DOI:10.1016/j.ecoenv.2019.03.027
摘要
Organophosphorus esters (OPEs), as one kind of emerging and toxic contaminant are ubiquitous in various environments. This study investigated the degradation of tris(2-chloroethyl) phosphate (TCEP) as a category OPEs by pyrite (FeS2)-activated persulfate (PS). The result shows that near-100% degradation of TCEP was achieved after 120 min in FeS2-PS system. The important role of Fe2+ in the activation mechanism was confirmed by the introduction of Fe2+ into the PS only system. Radical scavengers experiment and electron paramagnetic resonance (EPR) confirmed the presence of SO4·- and ·OH,which revealed that ·OH and SO4·- played major roles in TCEP degradation. The effect of various environmental factors, including pyrite and oxidant dosage, inorganic ions and pH were investigated. The result indicated that Fe3+ and Cl- can accelerate the degradation rate of TCEP and the reaction between TCEP and FeS2-PS favors acidic conditions (pH>9). In addition, due to the acidification of pyrite, this system can be applied with a wide pH range. Besides, two oxidation products, C4H9Cl2O4P and C2H6ClO4P were identified, which suggest that hydroxylation was probably the main mechanism. This study greatly improves our understanding on TCEP removal in FeS2-PS system.
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