UV/Sodium percarbonate for bisphenol A treatment in water: Impact of water quality parameters on the formation of reactive radicals

IF 11.4 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL
Jiong Gao , Roberta Frinhani Nunes , Kevin O'Shea , Greg L. Saylor , Lingjun Bu , Yu-Gyeong Kang , Xiaodi Duan , Dionysios D. Dionysiou , Shenglian Luo
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引用次数: 15

Abstract

Reported herein is an investigation of the impact of water quality parameters on the formation of carbonate radical anion (CO3) and hydroxyl radical (HO) in UV/sodium percarbonate (UV/SPC) system versus in UV/hydrogen peroxide (UV/H2O2) system for bisphenol A (BPA) degradation in water. Pathways of CO3 oxidation of BPA were proposed in this study based on the evolution of direct transformation products of BPA. Observed in this study, the degradation of BPA in the UV/SPC system was slower than that in the UV/H2O2 system in the secondary effluents collected from a local wastewater treatment plant due to the significant impact of coexisting constituents in the matrices on the former system. Single water quality parameter (e.g., solution pH, common anion, or natural organic matter) affected radical formations and BPA degradation in the UV/SPC system in a way similar to that in the UV/H2O2 system. Namely, the rise of solution pH decreased the steady state concentration of HO resulting in a decrease in the observed pseudo first-order rate constant of BPA (kobs). Chloride anion and sulfate anion played a negligible role over the examined concentrations; nitrate anion slightly suppressed the reaction at the concentration of 20 mM; bicarbonate anion decreased the steady state concentrations of both CO3 and HO exerting significant inhibition on BPA degradation. Different extents of HO scavenging were observed for different types of natural organic matter in the order of fulvic acid > mixed NOM > humic acid. However, the impact was generally less pronounced on BPA degradation in the UV/SPC system than that in the UV/H2O2 system due to the existence of CO3. The results of this study provide new insights into the mechanism of CO3 based oxidation and new scientific information regarding the impact of water quality parameters on BPA degradation in the sytems of UV/SPC and UV/H2O2 from the aspect of reactive radical formation, which have reference value for UV/SPC application in wastewater treatment.

Abstract Image

UV/过碳酸钠处理水中双酚A:水质参数对活性自由基形成的影响
本文报道了水质参数对紫外/过碳酸钠(UV/SPC)体系和紫外/过氧化氢(UV/H2O2)体系降解水中双酚A (BPA)时碳酸盐自由基阴离子(CO3•−)和羟基自由基(HO•)形成的影响。本研究基于BPA直接转化产物的演化,提出了BPA的CO3•−氧化途径。本研究发现,在当地某污水处理厂收集的二次出水中,由于基质中共存成分对前者系统的显著影响,在UV/SPC系统中BPA的降解速度比在UV/H2O2系统中慢。单个水质参数(例如,溶液pH、普通阴离子或天然有机物)在UV/SPC系统中影响自由基形成和BPA降解的方式与UV/H2O2系统相似。即,溶液pH的升高降低了HO•的稳态浓度,导致BPA (kobs)的伪一阶速率常数降低。氯离子和硫酸盐阴离子对检测浓度的影响可以忽略不计;硝酸阴离子在浓度为20 mM时对反应有轻微抑制作用;碳酸氢盐阴离子降低了CO3•−和HO•的稳态浓度,对BPA的降解有显著的抑制作用。对不同类型的天然有机物的HO•清除作用程度不同,其顺序为黄腐酸;混合NOM >胡敏酸。然而,由于CO3•−的存在,在UV/SPC体系中对BPA降解的影响通常不如在UV/H2O2体系中明显。本研究结果为CO3•−基氧化机理提供了新的认识,并从活性自由基形成方面为水质参数对UV/SPC和UV/H2O2体系中BPA降解的影响提供了新的科学信息,对UV/SPC在废水处理中的应用具有参考价值。
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来源期刊
Water Research
Water Research 环境科学-工程:环境
CiteScore
20.80
自引率
9.40%
发文量
1307
审稿时长
38 days
期刊介绍: Water Research, along with its open access companion journal Water Research X, serves as a platform for publishing original research papers covering various aspects of the science and technology related to the anthropogenic water cycle, water quality, and its management worldwide. The audience targeted by the journal comprises biologists, chemical engineers, chemists, civil engineers, environmental engineers, limnologists, and microbiologists. The scope of the journal include: •Treatment processes for water and wastewaters (municipal, agricultural, industrial, and on-site treatment), including resource recovery and residuals management; •Urban hydrology including sewer systems, stormwater management, and green infrastructure; •Drinking water treatment and distribution; •Potable and non-potable water reuse; •Sanitation, public health, and risk assessment; •Anaerobic digestion, solid and hazardous waste management, including source characterization and the effects and control of leachates and gaseous emissions; •Contaminants (chemical, microbial, anthropogenic particles such as nanoparticles or microplastics) and related water quality sensing, monitoring, fate, and assessment; •Anthropogenic impacts on inland, tidal, coastal and urban waters, focusing on surface and ground waters, and point and non-point sources of pollution; •Environmental restoration, linked to surface water, groundwater and groundwater remediation; •Analysis of the interfaces between sediments and water, and between water and atmosphere, focusing specifically on anthropogenic impacts; •Mathematical modelling, systems analysis, machine learning, and beneficial use of big data related to the anthropogenic water cycle; •Socio-economic, policy, and regulations studies.
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