Removal of polycyclic aromatic hydrocarbons (PAHs) from contaminated sewage sludge using advanced oxidation process (hydrogen peroxide and sodium persulfate)

被引:28
作者
Mokhtari, S. Ahmad [1 ]
Gholami, Mitra [2 ]
Dargahi, Abdollah [3 ]
Vosoughi, Mehdi [3 ]
机构
[1] Ardabil Univ Med Sci, Sch Hlth, Dept Environm Hlth Engn, Ardebil, Iran
[2] Iran Univ Med Sci, Sch Hlth, Dept Environm Hlth Engn, Tehran, Iran
[3] Ardabil Univ Med Sci, Social Determinants Hlth Res Ctr, Dept Environm & Occupat Hlth, Ardebil, Iran
关键词
Sewage sludge; Advanced oxidation; Persulfate; Polycyclic aromatic hydrocarbons; MECHANISM; KINETICS; TCE;
D O I
10.5004/dwt.2021.26716
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
This study has been carried out with the aim of evaluating the treatability of polycyclic aromatic hydrocarbon compounds of PAHs available in urban and industrial sewage sludge utilizing advanced chemical oxidation methods contingent on free sulfate radicals using hydrogen peroxide and heat activation methods. For this purpose, various parameters including (3, 5, 7, 9, and 10), persulfate's concentration (2, 10, 5, 15, and 20 mmol), the ratio of peroxide to persulfate (1, 0.5, 0.3, 0.2, and 0.1), sludge temperature (25 degrees C, 35 degrees C, 45 degrees C, and 55 degrees C) and the primary concentration of PAHs were considered at the 20 d reaction periods. Through making use of gas chromatography-mass spectrometry (GC-MS), after 40-min period, the quality and quantity of the compounds available in the samples were determined using a mass detector and the drawn standards curve. After examining the effectiveness of eliminating PAH compounds in various conditions, the chemical oxygen demand test was carried out for the samples related to optimal removal of PAH compounds to determine the real efficiency of the process in eliminating intermediate compounds originated from PAHs oxidation. The results demonstrate that the advanced chemical oxidation method (persulfate-peroxide) can effectively result in the elimination of PAH compounds from the sludge.
引用
收藏
页码:311 / 318
页数:8
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