Efficient chemical oxidation of high levels of soil-sorbed phenanthrene by ultrasound induced, thermally activated persulfate

被引:89
作者
Deng, Dayi [1 ]
Lin, Xueting [1 ]
Ou, Jianmin [1 ]
Wang, Zhen [1 ]
Li, Shuting [1 ]
Deng, Minling [1 ]
Shu, Yuehong [1 ]
机构
[1] S China Normal Univ, Sch Chem & Environm, Guangzhou 510006, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Persulfate; Ultrasound; Chemical oxidation; Phenanthrene; Hydrophobic organic contaminant; TERT-BUTYL ETHER; CONTAMINATED SOIL; DEGRADATION; SORPTION; TEMPERATURE; IDENTIFICATION; REMEDIATION; ANTHRACENE; SEDIMENTS; REMOVAL;
D O I
10.1016/j.cej.2014.12.055
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The sorption of hydrophobic organic contaminants (HOCs) and limited mass transfer in heterogeneous subsurface environment are major hurdles to efficient remediation of highly contaminated sites by traditional activated persulfate. In this work, ultrasound was coupled to persulfate oxidation to enhance the remediation. The mechanisms of the coupling process were investigated, using soil spiked with high levels of phenanthrene as a model compound for PAHs and other HOCs. The results indicate that, when ultrasound is applied to the soil slurry, the resultant heat, due to the ultrasonic energy absorbed by the soil particles, activates persulfate to generate sulfate radicals to oxidize the dissolved phenanthrene, and the dissolution and desorption of the phenanthrene are also enhanced by elevated temperature, ultrasound itself and the oxidation by persulfate, thereby creating a positive-feedback loop that induces rapid and highly efficient oxidation of the contaminants. Furthermore, the effects of ultrasound intensity, contaminant concentration, oxidant dosage, soil to water ratio, and addition of external activators on the oxidation of phenanthrene were also studied. For potential field applications, coupling downhole ultrasound technologies with traditional persulfate process was proposed to facilitate the remediation of HOCs contaminated sites. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:176 / 183
页数:8
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