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Kinetics and modeling of sulfonamide antibiotic degradation in wastewater and human urine by UV/H2O2 and UV/PDS

机译:UV / H2O2和UV / PDS降解废水和人尿中磺胺类抗生素的动力学和建模

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Sulfonamide antibiotks 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) x 10(9), (0.77-16.1) x 10(10) and (1.25-8.71) x 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. (C) 2016 Elsevier Ltd. All rights reserved.
机译:磺胺类抗生物素在水生环境中经常被发现,由于其不利的生物效应和诱导抗生素耐药性的潜力而引起人们的关注。这项研究调查了低压(LP)UV,UV / H2O2和UV /过氧二硫酸盐(PDS)对合成废水和水解人尿中磺酰胺类抗生素的降解动力学。磺酰胺类抗生素的直接光解速率有所不同,并取决于其结构。具有五元杂环基团的磺酰胺经历了更快的直接光解。对于间接光解过程,确定了具有羟基,硫酸根和碳酸根的磺酰胺类抗生素的二级速率常数,分别为(6.21-9.26)x 10(9),(0.77-16.1)x 10(10)和(分别为1.25-8.71)x 10(8)M-1 s(-1)。应用动力学模型并成功预测了磺酰胺在不同水基质中的降解动力学。在合成废水中,碳酸盐自由基约占总去除量的10%,而在合成水解尿液中,碳酸盐自由基是降解磺酰胺的主要反应物种。与合成废水相比,合成水解尿液中磺酰胺抗生素的清除效率更高,而UV / PDS降解紫外线磺酰胺的效率高于UV / H2O2。能量评估表明,在本研究应用的实验条件下,UV / PDS的能量消耗比LPUV和UV / H2O2少,特别是对于间接光解作用比直接光解作用强的磺酰胺类。通过改变紫外线剂量和氧化剂剂量,可以优化紫外线/过氧化氢工艺,以实现比合成废水中紫外线/ PDS工艺更高的效率。 (C)2016 Elsevier Ltd.保留所有权利。

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