School of Environmental Science and Engineering, Tianjin University, Tianjin 300072, China.
School of Civil and Environmental Engineering, Georgia Institute of Technology, Atlanta, GA 30332, United States.
Water Res. 2016 Oct 15;103:283-292. doi: 10.1016/j.watres.2016.07.037. Epub 2016 Jul 18.
Sulfonamide antibiotics have been frequently detected in the aquatic environment and are of emerging concern due to their adverse bio-effect and potential of inducing antibiotic resistance. This study investigated the degradation kinetics of sulfonamide antibiotics in synthetic wastewater and hydrolyzed human urine by low pressure (LP) UV, UV/H2O2 and UV/peroxydisulfate (PDS). Direct photolysis rates of sulfonamide antibiotics varied and depended on the structures. Sulfonamides with a five-membered heterocyclic group underwent faster direct photolysis. For indirect photolysis processes, second-order rate constants of sulfonamide antibiotics with hydroxyl radical, sulfate radical and carbonate radical were determined, which were (6.21-9.26) × 10(9), (0.77-16.1) × 10(10) and (1.25-8.71) × 10(8) M(-1) s(-1), respectively. A dynamic model was applied and successfully predicted the degradation kinetics of sulfonamides in different water matrices. In synthetic wastewater, carbonate radical contributed to approximately 10% of the overall removal, whereas in synthetic hydrolyzed urine, carbonate radical was the dominant reactive species to degrade sulfonamides. Sulfonamide antibiotics were eliminated more efficiently in synthetic hydrolyzed urine than in synthetic wastewater and UV/PDS was more efficient than UV/H2O2 to degrade most sulfonamides. Energy evaluation showed that UV/PDS costs less energy than LPUV and UV/H2O2 under the experimental conditions applied in this study, particularly for sulfonamides whose indirect photolysis overweighed direct photolysis. By varying UV dose and oxidant dose, the UV/H2O2 process can be optimized to achieve higher efficiency than the UV/PDS process in synthetic wastewater.
磺胺类抗生素经常在水环境中被检测到,由于其不良的生物效应和诱导抗生素耐药性的潜力,因此受到越来越多的关注。本研究通过低压 (LP) UV、UV/H2O2 和 UV/过二硫酸盐 (PDS) 研究了磺胺类抗生素在合成废水中和水解人尿中的降解动力学。磺胺类抗生素的直接光解速率不同,取决于其结构。具有五元杂环基团的磺胺类抗生素经历更快的直接光解。对于间接光解过程,确定了磺胺类抗生素与羟基自由基、硫酸根自由基和碳酸根自由基的二级速率常数,分别为 (6.21-9.26)×10(9)、(0.77-16.1)×10(10)和 (1.25-8.71)×10(8) M(-1) s(-1)。应用动态模型成功预测了不同水基质中磺胺类抗生素的降解动力学。在合成废水中,碳酸根自由基对总去除率的贡献约为 10%,而在合成水解尿中,碳酸根自由基是降解磺胺类抗生素的主要反应性物质。磺胺类抗生素在合成水解尿中的去除效率高于合成废水,并且 UV/PDS 比 UV/H2O2 更有效地降解大多数磺胺类抗生素。能量评估表明,在本研究中应用的实验条件下,UV/PDS 比 LPUV 和 UV/H2O2 消耗的能量更少,特别是对于间接光解超过直接光解的磺胺类抗生素。通过改变 UV 剂量和氧化剂剂量,可以优化 UV/H2O2 工艺,使其在合成废水中的效率高于 UV/PDS 工艺。