Degradation of trace aqueous 4-chloro-2-nitrophenol occurring in pharmaceutical industrial wastewater by ozone

被引:52
作者
Gharbani, P. [1 ]
Khosravi, M. [1 ]
Tabatabaii, S. M. [2 ]
Zare, K. [3 ]
Dastmalchi, S. [4 ]
Mehrizad, A. [2 ]
机构
[1] Islamic Azad Univ, Dept Chem, N Tehran Branch, Tehran, Iran
[2] Islamic Azad Univ, Dept Chem, Ahar Branch, Ahar, Iran
[3] Islamic Azad Univ, Dept Chem, Sci & Res Branch, Tehran, Iran
[4] Tabriz Univ Med Sci, Sch Pharm, Tabriz, Iran
关键词
Chemical oxygen demand; Degradation; Kinetic; Mineralization; Total organic carbon; PHOTOCATALYTIC OZONATION; CATALYTIC OZONATION; RATE CONSTANTS; OXIDATION; REMOVAL; PHENOL; 2,4,6-TRICHLOROPHENOL; BIODEGRADABILITY; PRODUCTS; DESIGN;
D O I
10.1007/BF03326147
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Degradation of 4-chloro-2-nitro phenol by ozonation in aqueous solution was studied in a semi batch reactor under constant ozone dosage and variable pH conditions. The effectiveness of the process was estimated based on the degree of conversion of 4-chloro-2-nitro phenol. It was observed that ozonation is more effective at alkaline reaction of medium than other conditions. The degree of conversion achieved (at the first 5 minutes of the process) at pH 9 was 99.64% compared to 99.03% and 77.35% at pH 7 and 3, respectively. Another parameter used to quantify the 4-chloro-2-nitrophenol during ozonation was the pseudo first order rate constant k [min(-1)]. Results showed that the rate constant of the process was approximately much higher at the alkaline pH compared to acidic ones. A considerable improvement in chemical oxygen demand removal was observed at pH above 7. At pH 9, the reduction in chemical oxygen demand at the end of the process reached 56.9 %. The degree of organically bounded nitrogen conversion to nitrate was higher at pH 3. Of the total organic carbon reduction, 15.89 % was observed at pH 9. The 4-chloro-2-nitro phenol degradation intermediate products were analyzed by mass-spectrometry. The main intermediate product was chlorophenol.
引用
收藏
页码:377 / 384
页数:8
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