State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, No. 163 Xianlin Avenue, Nanjing 210023, PR China.
State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, No. 163 Xianlin Avenue, Nanjing 210023, PR China.
Chemosphere. 2019 May;222:494-502. doi: 10.1016/j.chemosphere.2019.01.186. Epub 2019 Jan 31.
This study investigated the degradation of benzophenone-4 (BP-4) in a UV/chlorine disinfection process, with chlorination and UV disinfection as comparisons. With a degradation efficiency of 80% after 10 s, the UV/chlorine process significantly enhanced the degradation of BP-4. However, a rebound of 36% of the initial concentration was observed in the UV/chlorine process ([free active chlorine (FAC)]:[BP-4] = 1:1, pH = 7). The same tendency appeared under the addition of alkalinity, Cl, and humic acid (HA). This work interpreted this interesting kinetic tendency from the perspective of mechanism. In fact, the transformation between the chlorinated product P1 and BP-4 was reversible under certain conditions. The inhomogeneous charge distribution of the CCl bond in P1 led to the photolytic dechlorination of P1. This transformation caused an increase in BP-4 concentration. In addition, the increase in the UV light power promoted the photodecomposition of P1 under the experimental condition. In addition, this study evaluated the change in absorbable organic halogens (AOX) and three kinds of toxicity changes in the BP-4 solution after chlorination and the UV/chlorine process, including the acute toxicity of luminescent bacteria, endocrine disrupting effect and cytotoxicity. The UV/chlorine process exhibited lower ecotoxicity than chlorination in water treatment.
本研究考察了在 UV/氯消毒工艺中,二苯甲酮-4(BP-4)的降解情况,并与氯化和 UV 消毒进行了比较。在 10s 后,UV/氯工艺将 BP-4 的降解效率提高到 80%。然而,在 UV/氯工艺中([自由有效氯(FAC)]:[BP-4] = 1:1,pH = 7),观察到初始浓度的 36%反弹。在添加碱度、Cl 和腐殖酸(HA)的情况下,也出现了相同的趋势。本工作从机制的角度解释了这种有趣的动力学趋势。事实上,在某些条件下,氯化产物 P1 和 BP-4 之间的转化是可逆的。P1 中 CCl 键的不均匀电荷分布导致 P1 的光解脱氯。这种转化导致 BP-4 浓度增加。此外,在实验条件下,UV 光功率的增加促进了 P1 的光分解。此外,本研究评估了 BP-4 溶液在氯化和 UV/氯工艺后吸收性有机卤化物(AOX)和三种毒性变化的变化,包括发光细菌的急性毒性、内分泌干扰效应和细胞毒性。在水处理中,UV/氯工艺比氯化工艺具有更低的生态毒性。