光催化
二氧化钛
水消毒
废物管理
钛
水处理
二氧化氯
环境化学
环境科学
化学
制浆造纸工业
环境工程
材料科学
冶金
无机化学
催化作用
工程类
有机化学
作者
Brooke K. Mayer,Erin Daugherty,Morteza Abbaszadegan
出处
期刊:Chemosphere
[Elsevier]
日期:2014-06-25
卷期号:117: 72-78
被引量:31
标识
DOI:10.1016/j.chemosphere.2014.05.073
摘要
This study evaluated strategies targeting disinfection byproduct (DBP) mitigation using TiO2 photocatalysis with varying influent water quality. A Purifics Photo-CAT Lab reactor was used to assess total trihalomethane (TTHM) and haloacetic acid (HAA) formation as a function of photocatalytic treatment using water from a conventional coagulation/flocculation/sedimentation process, granular activated carbon filtration, and a DBP hot spot in the water distribution system. Regardless of influent water quality, photocatalysis reduced DBP precursors; however, low-energy limited photocatalysis (<5 kW h m−3), exacerbated the production of TTHMs and HAA5s beyond initial levels. Accordingly, limited photocatalysis is not a suitable option when TTHMs and HAA5s are a concern, regardless of the level of pretreatment. Limited photocatalysis yields incomplete oxidation, wherein larger, more aromatic, humic organic compounds are broken into smaller molecular weight, less aromatic, and less humic moieties, which have considerable potential to produce DBPs. More complete mineralization of DBP precursors is obtained using extended photocatalysis (80–160 kW h m−3), which substantially decreases DBP precursors as well as TTHM and HAA5 concentrations. In order to balance DBP mitigation, energy, and chemical usage, targeted use of TiO2 photocatalysis is necessary in a water treatment train (e.g., extended photocatalysis at a distribution system hot spot, where the volumetrically high energy requirements may be justifiable).
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