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Photodegradation of tetracycline and formation of reactive oxygen species in aqueous tetracycline solution under simulated sunlight irradiation

机译:模拟太阳光下四环素水溶液中四环素的光降解和活性氧的形成

摘要

The photochemical kinetics and mechanism of the antibiotic compound tetracycline (TC) was investigated in aqueous solution under simulated sunlight irradiation. The study of the electron spin resonance revealed that the singlet oxygen (O-1(2)) was generated and the formation rate decreased with increasing pH in illuminated TC solution. Also, it was found that the H2O2 was produced and increased with increasing pH under the simulated sunlight irradiation. The results verified that TC could be sunlight excited and induced the formation of reactive oxygen species. Moreover, the contributions of oxidation reaction to photodegraclation of TC were clarified by the role of different radical scavengers. The kinetic model elucidated the involvement of TC photoinduced singlet oxygen on the photodegradation of TC. It was verified that the photodegradation of TC was predominantly attributed to direct photolysis. The quantum yields of direct photolysis increases with increasing pH in the range of 6.0-9.0, varying from 3.4 x 10(-4) to 1.1 x 10(-2). The indirect photolysis of TC was carried out in the presence of nitrate, bicarbonate, ferric ions and humic acid (HA), respectively. The results verified that the photodegradation of tetracycline was not obviously affected by these photosensitizers except ferric ions, indicating that the direct photolysis of TC was predominant process. (c) 2007 Elsevier B.V. All rights reserved.
机译:在模拟阳光照射下,研究了水溶液中抗生素化合物四环素(TC)的光化学动力学和机理。电子自旋共振的研究表明,在光照的TC溶液中,产生了单线态氧(O-1(2)),且形成速率随pH的增加而降低。另外,还发现在模拟的阳光照射下,H2O2的产生和随着pH的增加而增加。结果证实TC可以被阳光激发并诱导活性氧的形成。此外,不同自由基清除剂的作用阐明了氧化反应对TC光脱盐的贡献。动力学模型阐明了TC光诱导的单线态氧与TC的光降解有关。证实TC的光降解主要归因于直接光解。直接光解的量子产率随pH值的增加在6.0-9.0范围内增加,范围从3.4 x 10(-4)到1.1 x 10(-2)。 TC的间接光解分别在硝酸根,碳酸氢根,铁离子和腐殖酸(HA)的存在下进行。结果证明,除铁离子外,这些光敏剂对四环素的光降解没有明显影响,表明TC的直接光解是主要过程。 (c)2007 Elsevier B.V.保留所有权利。

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