The role of quinone cycle in Fe2+-H2O2 system in the regeneration of Fe2+

被引:34
作者
Zhou, Wei [1 ]
Gao, Jihui [1 ]
Zhao, Haiqian [2 ]
Meng, Xiaoxiao [1 ]
Wu, Shaohua [1 ]
机构
[1] Harbin Inst Technol, Sch Energy Sci & Engn, 92 Dazhi St, Harbin 150001, Peoples R China
[2] Northeast Petr Univ, Sch Civil Engn & Architecture, Daqing, Peoples R China
基金
中国国家自然科学基金;
关键词
Fe2+-H2O2 system; hydroxyl radical; hydrogen peroxide; quinone cycle; Fe2+ regeneration; FENTON DEGRADATION; PHOTO-FENTON; HYDROGEN-PEROXIDE; OXIDATION; MECHANISM; DYES; ION;
D O I
10.1080/09593330.2016.1240241
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The reaction between Fe2+ and H2O2 generates highly reactive u OH. However, the weak conversion from Fe3+ to Fe2+ limits its continuous reaction. Here, the difference between the Fenton system and modified Fenton system for the regeneration of Fe2+ was analyzed. A UV-vis spectrometer and redox potential measurements were used to detect Fe2+ concentration. Results indicated that Fe2+ could be better regenerated in the modified Fenton system. The regeneration of Fe2+ was facilitated by the consumption of NH2OH, while in hydroquinone (HQ)-and 1,4-bezoquinone (1,4-BQ)-modified Fenton systems, the quinone cycle could be built up and Fe3+ could be converted to Fe2+ continuously. However, results showed that HQ and 1,4-BQ reacted with u OH, which caused a gradual decline in the enhancement effect. In order to keep Fe2+ concentration stable for a longer time, the influence of [HQ/ 1,4-BQ]0/[Fe2+] 0 on Fe2+ concentration was carefully studied. When the mole ratio was 5: 1, Fe2+ concentration remained nearly 90% of total iron at 40 min. But when the mole ratios were 0.5: 1 and 0.1: 1, Fe2+ concentration decreased to a very low level at 20 min. Oxidation-reduction potential (ORP) results further confirmed the role of quinone cycle. [GRAPHICS] .
引用
收藏
页码:1887 / 1896
页数:10
相关论文
共 50 条
  • [31] Piezo-promoted regeneration of Fe2+ boosts peroxydisulfate activation by Bi2Fe4O9 nanosheets
    Su, Chuangjian
    Li, Ruhong
    Li, Chaolin
    Wang, Wenhui
    APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY, 2022, 310
  • [32] The effect of H2O2/Fe2+ catalytic oxidation system on the morphology, structure and properties of flake-like poly(2,3-dimethylaniline)
    Yan, Jun
    Ma, Li
    Gan, Mengyu
    Li, Xiao
    Li, Zhitao
    Tang, Jihai
    Tu, Ying
    Hu, Haifeng
    MACROMOLECULAR RESEARCH, 2014, 22 (08) : 853 - 858
  • [33] Fe2O3@FeB composites facilitate heterogeneous Fenton process by efficient Fe(III)/Fe(II) cycle and in-situ H2O2 generation
    Wei, Kai
    Liu, Xiufan
    Cao, Shiyu
    Cui, Huijuan
    Zhang, Yu
    Ai, Zhihui
    CHEMICAL ENGINEERING JOURNAL ADVANCES, 2021, 8
  • [34] Comparative study of the oxidation of atrazine and acetone by H2O2/UV, Fe(III)/UV, Fe(III)/H2O2/UV and Fe(II) or Fe(III)/H2O2
    De Laat, J
    Gallard, H
    Ancelin, S
    Legube, B
    CHEMOSPHERE, 1999, 39 (15) : 2693 - 2706
  • [35] Comparative study of Fenton, Fe2+/NaOCl and Fe2+/(NH4)2S2O8 on tannery sludge dewaterability, degradability of organics and leachability of chromium
    Jessieleena, A. Angel
    Priyanka, M.
    Saravanakumar, M. P.
    JOURNAL OF HAZARDOUS MATERIALS, 2021, 402
  • [36] 1, 10-phenanthroline-Fe2+ oxidative assay of hydroxyl radical produced by H2O2/Fe2+
    Jin, M
    Cai, YX
    Li, JR
    Zhao, H
    PROGRESS IN BIOCHEMISTRY AND BIOPHYSICS, 1996, 23 (06) : 553 - 555
  • [37] Complementarity and action mechanisms of Fe2+-activated persulfate and H2O2 system
    Yu, Bolun
    Yao, Jingjing
    Li, Haipu
    Yang, Hui Ying
    APPLIED ORGANOMETALLIC CHEMISTRY, 2023, 37 (08)
  • [38] Microbial Oxidation of Fe2+ and Pyrite Exposed to Flux of Micromolar H2O2 in Acidic Media
    Ma, Yingqun
    Lin, Chuxia
    SCIENTIFIC REPORTS, 2013, 3
  • [39] Theoretical study on gas-phase electron transfer between Fe2+ and H2O2
    Zhao, HM
    Liu, K
    Li, ZH
    JOURNAL OF MOLECULAR STRUCTURE-THEOCHEM, 2004, 673 (1-3): : 115 - 119
  • [40] Sludge Reduction by H2O2 Oxidation with Fe/MgO Catalyst
    Cho, Sung Hoon
    Hwang, Duck Kun
    Um, Wooyong
    Son, Dae Hee
    Oh, Kyeongseok
    WATER ENVIRONMENT RESEARCH, 2015, 87 (08) : 675 - 682