水体pH与溶解性有机质对抗生素光化学转化动力学的协同影响机理

Mechanism of Synergistic Effect of pH and Dissolved Organic Matter in Water on Photochemical Transformation Kinetics of Antibiotics

  • 摘要: 光化学转化是水中抗生素类新污染物主要的消除途径,水体pH和溶解性有机质(DOM)是影响抗生素光化学转化的重要因素,但其协同影响机理尚不清楚。本文以诺氟沙星(NOR)和环丙沙星(CIP)作为抗生素代表,以Suwannee River天然有机质(SRNOM)和提取自松花江的DOM (S-DOM)作为DOM代表,在模拟太阳光照射下,通过光化学模拟实验和高效液相色谱检测法,研究了pH和DOM对抗生素光化学转化动力学的协同影响;通过探究不同pH值对DOM及其小分子类似物光敏化生成DOM激发三线态(3DOM*)、单线态氧(1O2)和羟基自由基(•OH)量子产率的影响,从分子层面阐明了影响机制。结果表明,pH=9.0时NOR的表观光解速率常数kobs (0.39min−1)分别是pH=5.0时(kobs=0.05min−1)和pH=7.0时(kobs=0.18min−1)的7.80倍和2.17倍,pH=9.0时CIP的kobs (0.43min−1)分别是pH=5.0时(kobs=0.05min−1)和pH=7.0时(kobs=0.20min−1)的8.60倍和2.15倍,即pH影响NOR和CIP的赋存形态进而直接影响其光化学转化,两种抗生素以两性离子形态存在时(pH=9.0)光化学转化最快,与前人结果一致。pH=9.0时DOM介导的抗生素的kobs分别是pH=5.0和pH=7.0时的7.20~14.00倍和1.87~2.25倍,1O2和•OH对抗生素光化学转化的促进作用最为显著,贡献率分别为36.50%和12.58%。光活性中间体(PPRIs)的贡献随pH增大而减弱,pH=5.0时贡献率为29.17%,pH=7.0时贡献率为16.00%。DOM的E2/E3等光物理性质和酚类等官能团可影响PPRIs的量子产率,pH影响DOM可解离组分的解离程度和DOM不可解离组分的氧化还原活性官能团进而改变PPRIs的量子产率,间接影响抗生素的光化学转化。综上,抗生素的光化学转化具有pH依赖性,DOM通过光敏化生成PPRIs促进抗生素的光化学转化。

     

    Abstract: Photochemical transformation is the main way to eliminate antibiotic emerging contaminants in aquatic environments. pH and dissolved organic matter (DOM) are important for photochemical transformation of antibiotics in water, yet their synergistic mechanism remains unclear. Norfloxacin (NOR) and ciprofloxacin (CIP) were taken as the representatives of antibiotics, while Suwannee River Natural Organic Matter (SRNOM) and DOM (S-DOM) extracted from Songhua River served as representatives of DOM. Through photochemical simulation experiments under simulated sunlight irradiation and high performance liquid chromatography, the synergistic effect of pH and DOM on the photochemical transformation kinetics of antibiotics was studied, and the molecular mechanism was elucidated by exploring how different pH values influenced quantum yields of excited triplet state (3DOM*), singlet oxygen (1O2), and hydroxyl radicals (•OH) generated by photosensitization of DOM and its small molecule analogues. As a result, the apparent photolysis rate constant (kobs) of NOR at pH=9.0 was 0.39min−1, which is 7.80 and 2.17 times higher than at pH=5.0 (kobs=0.05min−1) and pH=7.0 (kobs=0.18min−1), respectively. For CIP, the kobs at pH=9.0 (kobs=0.43min−1) is 8.60 and 2.15 times higher than that at pH=5.0 (kobs=0.05min−1) and pH=7.0 (kobs=0.20min−1), respectively. Therefore, pH, which influences occurrence forms of NOR and CIP, directly affects their photochemical transformation, and that of the two antibiotics is the fastest in the form of zwitterion (pH=9.0), consistent with previous results. The kobs of antibiotics mediated by DOM at pH=9.0 is 7.20–14.00 and 1.87–2.25 times higher than that at pH=5.0 and pH=7.0, respectively. 1O2 and •OH play the most significant role in promoting the photochemical transformation of antibiotics, with a contribution rate of 36.50% and 12.58% respectively, while the contribution of photochemically produced reactive intermediates (PPRIs) decreases as pH increases, with a contribution rate of 29.17% at pH=5.0, and 16.00% at pH=7.0. The photophysical properties (e.g., E2/E3) and functional groups (e.g., phenolic groups) can affect quantum yields of PPRIs, and pH, by influencing the dissociation degree of DOM dissociable components and the redox active functional groups of DOM non-dissociable components, changes quantum yields and indirectly impacts the photochemical transformation of antibiotics. In conclusion, the photochemical transformation of antibiotics is pH dependent, and DOM promotes the photochemical transformation of antibiotics by generating PPRIs through photosensitization. The BRIEF REPORT is available for this paper at http://www.ykcs.ac.cn/en/article/doi/10.15898/j.ykcs.202502100018.

     

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