降级(电信)
过硫酸盐
化学
天然有机质
催化作用
抗生素
激进的
可重用性
磺胺
人类健康
环境化学
核化学
有机质
生物化学
有机化学
电信
环境卫生
医学
程序设计语言
软件
计算机科学
作者
Zedi He,Qiongfang Wang,Pinhua Rao,Lei Dong,Min Zhang,Xin Zhang,Naiyun Gao,Jing Deng
标识
DOI:10.1016/j.scitotenv.2022.157987
摘要
The use of antibiotics has become an indispensable part of the production and life of human society. Among them, sulfonamide antibiotics widely used in humans and animals are considered to be one of the most crucial antibiotics. However, antibiotics are difficult to degrade naturally, leading to an accumulation in the environment and a potential hazard to human health. In this paper, WS2 as a co-catalyst could reduce trace Fe(III) to Fe(II) which exhibited a great activating ability to PS through the exposed W(IV) active sites, and formed the Fe(III)/Fe(II) cycle to degrade sulfachloropyridazine (SCP) continuously. This paper systematically discussed the degradation of SCP under different conditions in the PS/WS2/Fe(III) system, including the amount of WS2, Fe(III) concentration, PS concentration, initial pH, natural organic matter (NOM) and common anions (NO3-, Cl-, HCO3-, HPO42- and H2PO4-). The experimental results showed that PS/WS2/Fe(III) system possessed a strong degradation ability for SCP in a wide pH range. NO3- and Cl- could promote the degradation of SCP a little. HCO3-, HPO42- and H2PO4- could significantly inhibit the degradation of SCP. The main types of free radicals that degraded SCP were explored. In addition, the stability and reusability of WS2 were examined, and two possible degradation pathways of SCP were proposed.
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