Comparison of four pre-oxidants coupled powdered activated carbon adsorption for odor compounds and algae removal: Kinetics, process optimization, and formation of disinfection byproducts

化学 动力学 吸附 粉末活性炭处理 藻类 活性炭 过程(计算) 环境化学 碳纤维 化学工程 色谱法 制浆造纸工业 气味 有机化学 材料科学 植物 计算机科学 操作系统 物理 工程类 复合数 生物 量子力学 复合材料
作者
Heng-Xuan Zhao,Shuang Zhang,Tian‐Yang Zhang,Yiping Zhu,Ren-Jie Pan,Mengyuan Xu,Zheng-Xiong Zheng,Chenyan Hu,Yulin Tang,Bin Xu
出处
期刊:Science of The Total Environment [Elsevier BV]
卷期号:912: 168920-168920 被引量:10
标识
DOI:10.1016/j.scitotenv.2023.168920
摘要

Pre-oxidation and powdered activate carbon (PAC) are usually used to remove algae and odorants in drinking waterworks. However, the influence of interaction between oxidants and PAC on the treatment performance are scarcely known. This study systematically investigated the combination schemes of four oxidants (KMnO4, NaClO, ClO2, and O3) and PAC on the inactivation of Microcystis aeruginosa cells and removal of four frequently detected odorants in raw water (diethyl disulfide (DEDS), 2,2'-oxybis(1chloropropane) (DCIP), 2-methylisoborneol (2-MIB) and geosmin (GSM)). O3 showed highest pseudo-first-order removal rate for all four compounds and NaClO exhibited highest inactivation rates for the cell viability and Chlorophyll a (Chl-a). The Freundlich model fitted well for the adsorption of DEDS and DCIP by PAC. When treated by combined oxidation/PAC, the removal ratio of algae cells and odorants were lower (at least 1.6 times) than the sum of removal ratios obtained in oxidation or PAC adsorption alone. Among these four oxidants, the highest synchronous control efficiency of odorants (52 %) and algae (66 %) was achieved by NaClO/PAC. Prolonging the dosage time interval promoted the removal rates. The pre-PAC/post-oxidation processes possessed comparable efficiency for the removal of odorants and algae cells comparing with pre-oxidation/post-PAC process, but significantly inhibited formation of disinfection byproducts (DBPs), especially for the formation of C-DBPs (for NaClO and ClO2), bromate (for O3) and chlorate/chlorite (for ClO2). This study could provide a better understanding of improving in-situ operation of the combined pre-treatments of oxidation and PAC for source water.
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