Oxidation of propyl paraben by ferrate(VI): Kinetics, products, and toxicity assessment

被引:8
|
作者
An, Jibin [1 ]
Xia, Chunqiu [1 ]
He, Jiahong [1 ]
Feng, Huixia [2 ]
机构
[1] Chongqing Univ Arts & Sci, Chongqing Key Lab Environm Mat & Remediat Technol, Chongqing, Peoples R China
[2] Lanzhou Univ Technol, Sch Petrochem Engn, Lanzhou, Gansu, Peoples R China
来源
JOURNAL OF ENVIRONMENTAL SCIENCE AND HEALTH PART A-TOXIC/HAZARDOUS SUBSTANCES & ENVIRONMENTAL ENGINEERING | 2018年 / 53卷 / 10期
基金
中国国家自然科学基金;
关键词
Propyl paraben; ferrate(VI); degradation; kinetics; toxicity; RISK-ASSESSMENT; WASTE-WATER; PHARMACEUTICAL COMPOUNDS; DEGRADATION-PRODUCTS; ECOLOGICAL RISK; PROPYLPARABEN; MECHANISMS; TRANSFORMATIONS; CONTAMINANTS; OZONATION;
D O I
10.1080/10934529.2018.1459074
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Propyl paraben (propyl 4-hydroxybenzoate, PPB), one of the typically used paraben species in various pharmaceutical and personal care products, has been found in different aquatic environment, which could affect the water quality and human health. In this paper, the degradation of PPB by aqueous ferrate (Fe(VI)) was investigated in different water matrix and reaction kinetics as a function of pH was determined. Intermediate products of the degradation process were isolated and characterized by the high performance liquid chromatography/mass spectrometry/mass spectrometry techniques. Acute and chronic toxicities during water treatment of PPB using Fe(VI) were calculated using the ECOSAR program at three trophic levels. The obtained apparent second-order rate constant (k(app)) for PPB reaction with Fe(VI) ranged from 99.6 +/- 0.4M(-1) s(-1) to 15.0 +/- 0.1M(-1) s(-1) with the half-life (t(1/2)) ranging from 154s to 1026s at pH 6.5-10.0 for an Fe(VI) concentration of 600M. The proposed pathway for the oxidation of PPB by Fe(VI) involves one electron transfer of phenoxyl radical and breaking of the ether bond. In general, the oxidation of PPB by ferrate resulted in a significant decrease in toxicity at three trophic levels.
引用
收藏
页码:873 / 882
页数:10
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