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Item type:Item, Decomposition of 2-chlorophenol in aqueous solution by ultrasound/H2O2 process(1996) ;Lin, JG ;Chang, CN ;Wu, JR ;環境工程研究所Institute of Environmental EngineeringSeveral authors have indicated that ultrasound is effective in oxidizing organic contaminants in water and in wastewater either as the sole means of treatment or in combination with ozonation and UV irradiation. In this work we decomposed 2-chlorophenol (2-cp) in aqueous solution with ultrasound and H2O2. The experiment was conducted with a sonicator (Microson XL-2020) operated at 20 kHz. The double amplitude at the tip of the standard horn (12.7 mm) was adjusted to 0, 72 and 120 mu m, corresponding to power input 0, 125 and 160 W. The initial concentration of aqueous 2-cp solution was 100 mg/l, treated in the system with 0, 100, 200 and 500 mg/l H2O2 individually. The volume of solution was 11 in a mixing flask, and was circulated to the sonication cell at the rate 500 mL/min. Oxygen was continuously purged into the flask. The temperature of solution was kept constant at 25 degrees C and pH was controlled at 3, 5, 7, 9 and 11. The results showed the decomposition of 2-cp was effective at increased amplitude of ultrasound and concentration of H2O2, and smaller pH. At reaction duration 360 min, 2-cp decomposition with 500 mg/l H2O2 was found with 57% improvement over the control, i.e. without H2O2 addition. The pH, controlled below the pKa of 2-cp (8.49 at 25 degrees C), had significantly better decomposition of 2-cp than at greater values. The decomposition rate of 100 mg/l 2-cp was 99% at 120 mu m double amplitude with H2O2 (200 mg/L) and pH 3, after 360 min of reaction. The removal of total organic carbon was found to be only 63%. From analysis of the experimental results, the data on 2-cp decomposition appeared to follow pseudo-first-order reaction kinetics. The squared correlation coefficient, R2, of the model was greater than 0.9 for various pH values. Copyright (C) 1996 IAWQ.Item type:Item, Enhancement of decomposition of 2-chlorophenol with ultrasound/H2O2 process(1996) ;Lin, JG ;Chang, CN ;Wu, JR ;Ma, YS環境工程研究所We investigated the effects of pH, ionic strength, catalyst, and initial concentration on both decomposition of 2-chlorophenol (2-cp) and removal of total organic carbon (TOC) in aqueous solution with ultrasonic amplitude 120 mu m and H2O2 (200 mg/l). When the initial concentrations of 2-cp was 100 mg/l and the pH was controlled at 3, the rate of 2-cp decomposition was enhanced up to 6.6-fold and TOC removal up td 9.8-fold over pH controlled at 11. At pH 3, the efficiency of decomposition of 2-cp was 99% but the removal of TOC was only 63%; a similar situation applied at pH 7 and 11. Hence intermediate compounds were produced and 2-cp was not completely mineralized. When the concentration of ionic strength was increased from 0.001 to 0.1 M, the rate of 2-cp decomposition was enhanced only 0.3-fold, whereas the TOC removal was not enhanced. In comparison of the effects of pH and ionic strength, pH had greater influence on both 2-cp decomposition and TOC removal than ionic strength. The effect of a catalyst (FeSO4) on decomposition of 2-cp was insignificant comparing with direct addition of H2O2 The reaction rate at a smaller initial concentration of 2-cp (10 mg/l) was more rapid than at a greater one (100 mg/l). The rate of 2-cp decomposition and TOC removal appeared to follow pseudo-first-order reaction kinetics. Copyright (C) 1996 IAWQ. Published by Elsevier Science Ltd.