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Photodegradation of Carbamazepine, Ibuprofen, Ketoprofen and 17α-Ethinylestradiol in Fresh and Seawater

机译:淡水和海水中卡马西平,布洛芬,酮洛芬和17α-乙炔雌二醇的光降解

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Photodegradation of four pharmaceuticals (i.e. carbamazepine, ibuprofen, ketoprofen and 17α-ethinylestradiol) in aqueous media was studied using a solar light simulator (Xe lamp irradiation) and sunlight experiments. These experiments were carried out in river and seawater and compared to distilled water. The latter was used to evaluate the direct photodegradation pathways. Irradiation time was up to 400 min and 24 days for the solar light simulator and sunlight assays, respectively. Pharmaceutical photodegradation followed a first-order kinetics and their half-lives calculated in every aqueous matrix. Moreover, the sensitizing effect of DOC was evaluated by comparison with the kinetics obtained in distilled waters. Ketoprofen was rapidly transformed via direct photolysis in all the waters under both sunlight (t 1/2 = 2.4 min) and simulated solar light simulator test (t 1/2 = 0.54 min). Under xenon lamp radiation, ibuprofen and 17α-ethinylestradiol were photodegraded at moderate rate with half-lives from 1 to 5 h. Finally, carbamazepine had the lowest photodegradation rate (t 1/2 = 8–39 h) attributable to indirect photodegradation. Indeed, its elimination was strongly dependent on the DOC concentration present in solution. Finally, several ketoprofen photoproducts were identified and plotted against solar light simulator irradiation time. Accordingly, the photodegradation pathway of ketoprofen was postulated.
机译:使用太阳光模拟器(氙灯照射)和日光实验研究了四种药物(即卡马西平,布洛芬,酮洛芬和17α-炔雌醇)在水性介质中的光降解作用。这些实验是在河流和海水中进行的,并与蒸馏水进行了比较。后者用于评估直接的光降解途径。对于太阳光模拟器和日光测定法,辐照时间分别长达400分钟和24天。药物光降解遵循一阶动力学,并在每种水性基质中计算其半衰期。此外,通过与在蒸馏水中获得的动力学进行比较来评估DOC的敏化作用。在阳光下(t 1/2 = 2.4 min)和模拟太阳光模拟器测试(t 1/2 = 0.54)下,酮洛芬在所有水中均通过直接光解而迅速转化。分钟)。在氙灯辐射下,布洛芬和17α-炔雌醇以中等速率被光降解,半衰期为1至5小时。最后,卡马西平的光降解速率最低(t 1/2 = 8–39 h),可归因于间接光降解。实际上,其消除在很大程度上取决于溶液中存在的DOC浓度。最后,确定了几种酮洛芬光产品,并针对太阳光模拟器的照射时间作图。因此,推测了酮洛芬的光降解途径。

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