Xue Honghai, Gao Siyu, Zheng Na, Li Ming, Wen Xue, Wei Xindong
Key Laboratory of Groundwater Resources and Environment, Ministry of Education, Jilin University, Changchun 130021, China E-mail:
Key Laboratory of Songliao Aquatic Environment, Ministry of Education, Jilin Jianzhu University, Changchun 130118, China.
Water Sci Technol. 2019 Jun;79(12):2387-2394. doi: 10.2166/wst.2019.240.
The frequent detection of antibiotics in water bodies gives rise to concerns about their removal technology. In this study, the degradation kinetics and mechanisms of norfloxacin (NOR), a typical fluoroquinolone pharmaceutical, by the UV/peroxydisulfate (PDS) was investigated. NOR could be degraded effectively using this process, and the degradation rate increased with the increasing dosage of PDS but decreased with the increasing concentration of NOR. In real water, the degradation of NOR was slower than that in ultrapure water, which indicated that laboratory results cannot be directly used to predict the natural fate of antibiotics. Further experiments suggested that the degradation of NOR was the most fast under neutral condition, the existence of HA or FA inhibited the degradation of NOR, and the presence of inorganic ions (NO , Cl, CO and HCO ) had no significant effect on degradation of NOR. Total organic carbon (TOC) removal rate (40%) indicated NOR was not completely mineralized, and six transformation products were identified, and possible degradation pathways of NOR had been proposed. It can be prospected that UV/PDS technology could be used for advanced treatment of wastewater containing fluoroquinolones.
水体中频繁检测到抗生素引发了对其去除技术的关注。在本研究中,考察了典型氟喹诺酮类药物诺氟沙星(NOR)在紫外/过硫酸盐(PDS)作用下的降解动力学和机制。采用该工艺可有效降解NOR,降解速率随PDS投加量的增加而增大,但随NOR浓度的增加而减小。在实际水体中,NOR的降解比在超纯水中慢,这表明实验室结果不能直接用于预测抗生素的自然归趋。进一步实验表明,NOR在中性条件下降解最快,HA或FA的存在抑制了NOR的降解,无机离子(NO 、Cl、CO 和HCO )的存在对NOR的降解无显著影响。总有机碳(TOC)去除率(40%)表明NOR未完全矿化,鉴定出六种转化产物,并提出了NOR可能的降解途径。可以预期,UV/PDS技术可用于含氟喹诺酮类废水的深度处理。