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Degradation of bisphenol-A using ultrasonic irradiation assisted by low-concentration hydrogen peroxide 被引量:9

Degradation of bisphenol-A using ultrasonic irradiation assisted by low-concentration hydrogen peroxide
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摘要 This study investigated the degradation of bisphenol-A (BPA) by ultrasonic irradiation in the presence of different additives (H2O2, air bubbles and humic acid) under various operating conditions, i.e., ultrasonic frequency, power intensity and power density. The results demonstrated that the BPA degradation followed pseudo first-order kinetics under different experimental conditions. The optimum power intensities were 0.9, 1.8, and 3.0 W/cm2 at the frequencies of 400, 670, and 800 kHz, respectively. At the fixed frequency (800 kHz), the degradation rate of BPA was shown proportional to the increase of power density applied. With this manner, the BPA sonolysis could be facilitated at H202 dosage being lower than 0.1 mmol/L; while BPA degradation was hindered at H202 concentration in excess of 1 mmol/L. Additionally, BPA removal was shown to be inhibited by the presence of aeration and humic acid during ultrasonic irradiation. The present study suggested that the degradation rate of BPA assisted by ultrasonic irradiation was influenced by a variety of factors, and high BPA removal rate could be achieved under appropriate conditions. This study investigated the degradation of bisphenol-A (BPA) by ultrasonic irradiation in the presence of different additives (H2O2, air bubbles and humic acid) under various operating conditions, i.e., ultrasonic frequency, power intensity and power density. The results demonstrated that the BPA degradation followed pseudo first-order kinetics under different experimental conditions. The optimum power intensities were 0.9, 1.8, and 3.0 W/cm2 at the frequencies of 400, 670, and 800 kHz, respectively. At the fixed frequency (800 kHz), the degradation rate of BPA was shown proportional to the increase of power density applied. With this manner, the BPA sonolysis could be facilitated at H202 dosage being lower than 0.1 mmol/L; while BPA degradation was hindered at H202 concentration in excess of 1 mmol/L. Additionally, BPA removal was shown to be inhibited by the presence of aeration and humic acid during ultrasonic irradiation. The present study suggested that the degradation rate of BPA assisted by ultrasonic irradiation was influenced by a variety of factors, and high BPA removal rate could be achieved under appropriate conditions.
出处 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2011年第1期31-36,共6页 环境科学学报(英文版)
基金 supported by the National Natural Science Foundation of China (No.50878163,50708067) the National Major Project of Science & Technology Ministry of China (No.2008ZX07421-002) the National High Technology Research and Development Program (863) of China (No.2008AA06A412) the Research and Development Project of Ministry of Housing and Urban-Rural Development (No. 2009-K7-4)
关键词 bisphenol-A (BPA) ultrasonic irradiation power density ADDITIVES bisphenol-A (BPA) ultrasonic irradiation power density additives
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