Core Chinese Journal
Source Journal of CSCD(Core Version)
Source Journal for Chinese Scientific and Technical Papers
Core Journal of RCCSE
Included in JST China
Volume 40 Issue 5
Jul.  2022
Turn off MathJax
Article Contents
JIE Ya-wei, XU Ran-yun, DING Wei, JIANG Yi-heng, ZHANG Ben, LIU Hong-yuan. AOX FORMATION DURING THE ADVANCED OXIDATION OF PHENOL WASTEWATER CONTAINING CHLORIDE ION[J]. ENVIRONMENTAL ENGINEERING , 2022, 40(5): 1-8. doi: 10.13205/j.hjgc.202205001
Citation: JIE Ya-wei, XU Ran-yun, DING Wei, JIANG Yi-heng, ZHANG Ben, LIU Hong-yuan. AOX FORMATION DURING THE ADVANCED OXIDATION OF PHENOL WASTEWATER CONTAINING CHLORIDE ION[J]. ENVIRONMENTAL ENGINEERING , 2022, 40(5): 1-8. doi: 10.13205/j.hjgc.202205001

AOX FORMATION DURING THE ADVANCED OXIDATION OF PHENOL WASTEWATER CONTAINING CHLORIDE ION

doi: 10.13205/j.hjgc.202205001
  • Received Date: 2021-06-25
    Available Online: 2022-07-02
  • The high concentration of chloride ions prevalent in refractory industrial wastewater affects the performance of advanced oxidation and generates harmful organochlorine by-products. In this study, phenol was selected as the target pollutant and the generation of adsorbable organic halogens(AOX) during its oxidation by two typical advanced oxidation processes, namely UV/PDS and UV/H2O2, were investigated in the presence of Cl-. The results showed that UV/PDS was more effective than UV/H2O2 in the degradation and mineralization of phenol under experimental conditions in the presence of 1000 mg/L and 10000 mg/L Cl-. However, the AOX concentration formed during UV/PDS oxidation was about 10 times higher than that in UV/H2O2. The UV/H2O2 process tended to form more AOX under strongly acidic conditions(pH=3), while the AOX generation in the UV/PDS process was not significantly affected by the initial pH. Simulations of the steady-state concentrations of the four chlorine radicals revealed that the chlorine radical concentration increased for 1~2 orders of magnitude, when Cl- increased from 1000 mg/L to 10000 mg/L. The concentration in the UV/PDS system was significantly higher than that in UV/H2O2, which may be an important reason for the significant difference in AOX observed in the two advanced oxidation processes under different conditions. Similarly, the UV/PDS generated more AOX when treating actual wastewater, and the effect of organic structure and composition in wastewater on AOX generation was stronger than the effect of TOC concentration in wastewater.
  • loading
  • [1]
    MA D S,YI H,LAI C,et al.Critical review of advanced oxidation processes in organic wastewater treatment[J].Chemosphere,2021,275:130104.
    [2]
    GIANNAKIS S,LIN K Y A,GHANBARI F.A review of the recent advances on the treatment of industrial wastewaters by sulfate radical-based advanced oxidation processes (SR-AOPs)[J].Chemical Engineering Journal,2021,406:127083.
    [3]
    TU X,MENG X Y,PAN Y,et al.Degradation kinetics of target compounds and correlations with spectral indices during UV/H2O2 post-treatment of biologically treated acrylonitrile wastewater[J].Chemosphere,2020,243:125384.
    [4]
    OYEKUNLE D T,CAI J,GENDY E A,et al.Impact of chloride ions on activated persulfates based advanced oxidation process (AOPs):a mini review[J].Chemosphere,2021,280:130949.
    [5]
    XIE Y W,XU R Y,LIU R,et al.Adsorbable organic halogens formed during treatment of Cl--containing wastewater by sulfate and hydroxyl radical-based advanced oxidation processes[J].Chemical Engineering Journal,2020,389:124457.
    [6]
    HU L M,ZHANG G S,LIU M,et al.Enhanced degradation of Bisphenol A (BPA) by peroxymonosulfate with Co3O4-Bi2O3 catalyst activation:effects of pH,inorganic anions,and water matrix[J].Chemical Engineering Journal,2018,338:300-310.
    [7]
    WANG Y B,CAO D,ZHAO X.Heterogeneous degradation of refractory pollutants by peroxymonosulfate activated by CoOx-doped ordered mesoporous carbon[J].Chemical Engineering Journal,2017,328:1112-1121.
    [8]
    ANIPSITAKIS G P,DIONYSIOU D D,GONZALEZ M A.Cobalt-mediated activation of peroxymonosulfate and sulfate radical attack on phenolic compounds:implications of chloride ions[J].Environmental Science& Technology,2006,40(3):1000-1007.
    [9]
    YUAN R,RAMJAUN S N,WANG Z,et al.Photocatalytic degradation and chlorination of azo dye in saline wastewater:Kinetics and AOX formation[J].Chemical Engineering Journal,2012,192:171-178.
    [10]
    FANG C L,XIAO D X,LIU W Q,et al.Enhanced AOX accumulation and aquatic toxicity during 2,4,6-trichlorophenol degradation in a Co (Ⅱ)/peroxymonosulfate/Cl- system[J].Chemosphere,2016,144:2415-2420.
    [11]
    KACZMARCZYK A,NIEMIRYCZ E.Adsorbable organic halogens (AOX) in polish rivers-levels and changes[J].Acta Hydrochimica et Hydrobiologica,2005,33(4):324-336.
    [12]
    XU R Y,XIE Y W,TIAN J P,et al.Adsorbable organic halogens in contaminated water environment:a review of sources and removal technologies[J].Journal of Cleaner Production,2021,283:124645.
    [13]
    YANG W C,LI X M,XI D D,et al.Synergistic chromium (Ⅵ) reduction and phenol oxidative degradation by FeS2/Fe0 and persulfate[J].Chemosphere,2021,281:130957.
    [14]
    任龙飞,徐宇博,邵嘉慧.新型PDMS相转化膜在萃取膜生物反应器中的应用[J].环境工程,2021,39(7):133-138.
    [15]
    XIE Y W,CHEN L J,LIU R,et al.AOX contamination in Hangzhou Bay,China:Levels,distribution and point sources[J].Environmental Pollution,2018,235:462-469.
    [16]
    OLMEZ-HANCI T,ARSLAN-ALATON I.Comparison of sulfate and hydroxyl radical based advanced oxidation of phenol[J].Chemical Engineering Journal,2013,224:10-16.
    [17]
    ESPLUGAS S,GIMENEZ J,CONTRERAS S,et al.Comparison of different advanced oxidation processes for phenol degradation[J].Water Research,2002,36(4):1034-1042.
    [18]
    GREBEL J E,PIGNATELLO J J,MITCH W A.Effect of halide ions and carbonates on organic contaminant degradation by hydroxyl radical-based advanced oxidation processes in saline waters[J].Environmental Science& Technology,2010,44(17):6822-6828.
    [19]
    STEFAN M I,HOY A R,BOLTON J R.Kinetics and mechanism of the degradation and mineralization of acetone in dilute aqueous solution sensitized by the UV photolysis of hydrogen peroxide[J].Environmental Science& Technology,1996,30(7):2382-2390.
    [20]
    LEE Y M,LEE G,ZOH K D.Benzophenone-3 degradation via UV/H2O2 and UV/persulfate reactions[J].Journal of Hazardous Materials,2021,403:123591.
    [21]
    HUANG Y F,HUANG Y H.Identification of produced powerful radicals involved in the mineralization of bisphenol A using a novel UV-Na2S2O8/H2O2-Fe (Ⅱ,Ⅲ) two-stage oxidation process[J].Journal of Hazardous Materials,2009,162(2/3):1211-1216.
    [22]
    LIU J,LIU Y,TIAN Y,et al.Comparison of the oxidation of halogenated phenols in UV/PDS and UV/H2O2 advanced oxidation processes[J].RSC Advances,2020,10(11):6464-6472.
    [23]
    LUTZE H V,KERLIN N,SCHMIDT T C.Sulfate radical-based water treatment in presence of chloride:formation of chlorate,inter-conversion of sulfate radicals into hydroxyl radicals and influence of bicarbonate[J].Water Research,2015,72:349-360.
    [24]
    YANG Y,PIGNATELLO J J,MA J,et al.Comparison of halide impacts on the efficiency of contaminant degradation by sulfate and hydroxyl radical-based advanced oxidation processes (AOPs)[J].Environmental Science& Technology,2014,48(4):2344-2351.
    [25]
    WANG Z H,YUAN R X,GUO Y G,et al.Effects of chloride ions on bleaching of azo dyes by Co2+/oxone regent:kinetic analysis[J].Journal of Hazardous Materials,2011,190(1/2/3):1083-1087.
    [26]
    WANG F G,WANG W J,YUAN S J,et al.Comparison of UV/H2O2 and UV/PS processes for the degradation of thiamphenicol in aqueous solution[J].Journal of Photochemistry and Photobiology a-Chemistry,2017,348:79-88.
    [27]
    GHALY M Y,HARTEL G,MAYER R,et al.Photochemical oxidation of p-chlorophenol by UV/H2O2 and photo-Fenton process:a comparative study[J].Waste Management,2001,21(1):41-47.
    [28]
    PEIRO A M,AYLLON J A,PERAL J,et al.TIO2-photocatalyzed degradation of phenol and ortho-substituted phenolic compounds[J].Applied Catalysis B-Environmental,2001,30(3/4):359-373.
    [29]
    FANG J Y,FU Y,SHANG C.The roles of reactive species in micropollutant degradation in the UV/free chlorine system[J].Environmental Science& Technology,2014,48(3):1859-1868.
    [30]
    IANNI J C.Kintecus,Windows version V6.51[Z].2018;Available from:http://kintecus.com/.
    [31]
    BAYCAN N,THOMANETZ E,SENGUL F.Influence of chloride concentration on the formation of AOX in UV oxidative system[J].Journal of Hazardous Materials,2007,143(1/2):171-176.
    [32]
    MINISCI F,CITTERIO A,GIORDANO C.Electron-transfer processes-peroxydisulfate,a useful and versatile reagent in organic-chemistry[J].Accounts of Chemical Research,1983,16(1):27-32.
    [33]
    李卫平,郝梦影,敬双怡,等.SMBBR处理焦化废水性能及菌群结构响应关系[J].中国环境科学,2019,39(8):3332-3339.
    [34]
    LU J H,BENJAMIN M M,KORSHIN G V,et al.Reactions of the flavonoid hesperetin with chlorine:a spectroscopic study of the reaction pathways[J].Environmental Science& Technology,2004,38(17):4603-4611.
  • 加载中

Catalog

    通讯作者: 陈斌, bchen63@163.com
    • 1. 

      沈阳化工大学材料科学与工程学院 沈阳 110142

    1. 本站搜索
    2. 百度学术搜索
    3. 万方数据库搜索
    4. CNKI搜索

    Article Metrics

    Article views (508) PDF downloads(30) Cited by()
    Proportional views
    Related

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return