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光照射过程中土霉素水溶液的降解及降解产物的毒性变化

Aqueous oxytetracycline degradation and the toxicity change of degradation compounds in photoirradiation process.

作者信息

Jiao Shaojun, Zheng Shourong, Yin Daqiang, Wang Lianhong, Chen Liangyan

机构信息

State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing 210093, China.

出版信息

J Environ Sci (China). 2008;20(7):806-13. doi: 10.1016/s1001-0742(08)62130-0.

Abstract

The extensive use of antibiotics has been a worldwide environmental issue. In this study the fate of oxytetracycline (OTC), under photoirradiation, was investigated. The results showed that OTC photolysis followed first order model kinetics. Direct photolysis rate was found to be dependent on the initial OTC concentration, with k value ranging from 0.0075 to 0.0141 min(-1), in the OTC concentration from 40 to 10 mg/L. OTC photolysis was highly pH-dependent and strongly enhanced at a high pH value, with a k value of 0.0629 min(-1) at pH 9. Enhanced OTC photolysis has also been observed in the presence of nitrate and low concentration of dissolved organic matter. Upon irradiation for 240 min, only 13.5% reduction of TOC occured in spite of a rapid consumption of 90% of OTC. The byproducts from OTC photolysis have been analyzed using high-performance liquid chromatography electrospray ionization mass spectrometry (LC-ESI-MS), and the degradation pathway of OTC in the photo process was proposed. By employing luminescent bacterium to assess the adversity of the degradation compounds, an increased effect of toxicity occured in spite of the great consumption of OTC in the photoirradiation process. After irradiation for 240 min, the inhibition rate was 47%, significantly higher than the initial rate of 21% (p < 0.05), revealing a potentially higher adversity risk on the microorganism upon OTC photolysis.

摘要

抗生素的广泛使用已成为一个全球性的环境问题。在本研究中,考察了土霉素(OTC)在光照射下的归宿。结果表明,OTC光解遵循一级模型动力学。发现直接光解速率取决于初始OTC浓度,在OTC浓度为40至10mg/L时,k值范围为0.0075至0.0141min⁻¹。OTC光解高度依赖于pH值,在高pH值下强烈增强,在pH9时k值为0.0629min⁻¹。在硝酸盐和低浓度溶解有机物存在下也观察到OTC光解增强。照射240分钟后,尽管90%的OTC迅速消耗,但总有机碳(TOC)仅减少了13.5%。使用高效液相色谱电喷雾电离质谱(LC-ESI-MS)分析了OTC光解的副产物,并提出了OTC在光过程中的降解途径。通过使用发光细菌评估降解化合物的危害性,尽管在光照射过程中OTC大量消耗,但毒性效应仍有所增加。照射240分钟后,抑制率为47%,显著高于初始率21%(p<0.05),表明OTC光解对微生物具有潜在更高的危害风险。

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