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模型沉積物中POPs的超聲波降解

Sonochemical deg radation of POPs in model sediment

  • 摘要: 以六氯苯為例,用超聲波輻射及與其它高級氧化技術(AOPs)相結合來降解持久性有機污染物(POPs).結果表明,當超聲波輻射與紫外線輻射結合時,六氯苯的降解率與單一超聲波輻射降解率幾乎相同,分別為39.7%和40.0%;而當超聲波輻射與光催化相結合時,由于所添加的TiO2顆粒促進了空穴的形成,降解率可提高到49.4%;當表面活性劑的質量分數提高到0.1%時,降解率可提高到49.2%;當用雙頻超聲波輻射時,六氯苯的降解率高于任一單頻超聲波輻射.經過1 h超聲波輻射,20/176 kHz雙頻、20 kHz單頻和176單頻條件下,六氯苯降解率分別為57.5%,3.67%和41.0%.

     

    Abstract: The potential of hexachlorobenzen(HCB),one of POPs,decomposition by ultrasonic irradiation and its combination with other AOPs(advanced chemical oxidation processes) and surfactant addition was evaluated.Comparing the ultrasonic irradiation alone with the combination with the UV(ultraviolet) light irradiation,the degradation ratios were almost the same,40.0% and 39.7%,respectively.On the other hand,the degradation ratio increased to 49.4% when combining with photocatalysis possibly attributed to the promotion of the cavitation due to the addition of TiO2 particles.When the surfactant concentration was increased to 0.1%,the degradation ratio increased to 49.2%.It seemed that the added surfactant could contribute to desorbing HCB from the sediment surface and increasing the effective reaction surface area.The degradation ratio of HCB under the dual-frequency ultrasonic irradiation was higher than that under the mono-frequency ultrasonic irradiation.After 1 h ultrasonic irradiation,the degradation ratio was 57.5% for the dual-frequency ultrasound of 20/176 kHz combination,whereas 3.67% and 41.0% for 20 and 176 kHz ultrasound,respectively.

     

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