The degradation of diethyl phthalate (DEP) during ozonation: oxidation by-products study

被引:24
|
作者
Jung, Yeon Jung [1 ]
Oh, Byung Soo [2 ]
Kim, Kyoung Suk [3 ]
Koga, Minoru [4 ]
Shinohara, Ryota [4 ]
Kang, Joon-Wun [1 ]
机构
[1] Yonsei Univ, YIEST, Dept Environm Engn, Wonju 220710, South Korea
[2] Ctr Seawater Desalinat Plant, Kwangju 500712, South Korea
[3] Future Dev Inst, Masan, Gyeongsangnam D, South Korea
[4] Prefectural Univ Kumamoto, Fac Environm & Symbiot Sci, Kumamoto 8628502, Japan
关键词
degradation; diethyl phthalate (DEP); hydroxyl radical; intermediates; ozone; MEDIATED PHOTOCATALYTIC DEGRADATION; WATER TREATMENT PLANTS; ESTROGENIC ACTIVITY; DIBUTYL PHTHALATE; BISPHENOL-A; ESTERS; MICROPOLLUTANTS; MINERALIZATION; PLASTICIZERS; MECHANISM;
D O I
10.2166/wh.2009.301
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The degradation of diethyl phthalate (DEP) in an aqueous solution during ozonation was investigated by identifying the oxidation intermediates using GC-MS. The experiments were carried out in semi-batch mode with a 1.5 mg l(-1)-min ozone dose. The proposed degradation pathways were divided into hydrolysis of the aliphatic chain (pathway (A)) and hydroxylation resulting from center dot OH attack in the aromatic ring (pathway (B)). With increasing ozone dose, the aromatic ring of DEP was opened and acidic compounds, such as malonic acid, succinic acid and glutaric acid were formed. In addition, the ozonation of DEP for 18 min induced hydrogen peroxide (H2O2) generation at levels six times higher than pure water. Of the intermediates indentified, phthalic acid (PA) and phthalic anhydride (PAH) enhanced the degradation of DEP by promoting ozone decomposition.
引用
收藏
页码:290 / 298
页数:9
相关论文
共 50 条
  • [1] Degradation of diethyl phthalate (DEP) by vacuum ultraviolet process: influencing factors, oxidation products, and toxicity assessment
    Wu, Yangtao
    Deng, Lin
    Bu, Lingjun
    Zhu, Shumin
    Shi, Zhou
    Zhou, Shiqing
    ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH, 2019, 26 (06) : 5435 - 5444
  • [2] Degradation of diethyl phthalate (DEP) by vacuum ultraviolet process: influencing factors, oxidation products, and toxicity assessment
    Yangtao Wu
    Lin Deng
    Lingjun Bu
    Shumin Zhu
    Zhou Shi
    Shiqing Zhou
    Environmental Science and Pollution Research, 2019, 26 : 5435 - 5444
  • [3] Significant diethyl phthalate (DEP) degradation by combined advanced oxidation process in aqueous solution
    Na, Seungmin
    Ahn, Yun-Gyong
    Cui, Mingcan
    Khim, Jeehyeong
    JOURNAL OF ENVIRONMENTAL MANAGEMENT, 2012, 101 : 104 - 110
  • [4] Sonophotolytic diethyl phthalate (DEP) degradation with UVC or VUV irradiation
    Na, Seungmin
    Jinhua, Cai
    Cui, Mingcan
    Khim, Jeehyeong
    ULTRASONICS SONOCHEMISTRY, 2012, 19 (05) : 1094 - 1098
  • [5] Photocatalytic Degradation of Diethyl Phthalate (DEP) in Water Using TiO2
    Wen-Bin Huang
    Chih-Yu Chen
    Water, Air, and Soil Pollution, 2010, 207 : 349 - 355
  • [6] Photocatalytic Degradation of Diethyl Phthalate (DEP) in Water Using TiO2
    Huang, Wen-Bin
    Chen, Chih-Yu
    WATER AIR AND SOIL POLLUTION, 2010, 207 (1-4): : 349 - 355
  • [7] Ozonation of metoprolol in aqueous solution: ozonation by-products and mechanisms of degradation
    Tay, Kheng Soo
    Abd Rahman, Noorsaadah
    Bin Abas, Mhd Radzi
    ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH, 2013, 20 (05) : 3115 - 3121
  • [8] Ozonation of acebutolol in aqueous solution: Ozonation by-products and degradation pathway
    Tay, Kheng Soo
    Madehi, Norfazrina
    SEPARATION AND PURIFICATION TECHNOLOGY, 2014, 135 : 48 - 63
  • [9] Ozonation of metoprolol in aqueous solution: ozonation by-products and mechanisms of degradation
    Kheng Soo Tay
    Noorsaadah Abd. Rahman
    Mhd. Radzi Bin Abas
    Environmental Science and Pollution Research, 2013, 20 : 3115 - 3121
  • [10] Degradation of diethyl phthalate (DEP) by UV/persulfate: An experiment and simulation study of contributions by hydroxyl and sulfate radicals
    Wang, Ziying
    Shao, Yisheng
    Gao, Naiyun
    Lu, Xian
    An, Na
    CHEMOSPHERE, 2018, 193 : 602 - 610