光催化过程中选定雌激素和异种雌激素分解的比较研究

Edyta Burdzik-Niemiec, M. Dudziak
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摘要

本研究研究了三种不同的内分泌干扰化合物(EDCs),即17 -雌二醇(E2), 17 -乙基雌二醇(EE2)和双酚A (BPA)在光催化过程(UV/TiO2)中的降解效率。该研究的主题是一个含有无机和任选有机物质的合成城市污水处理厂流出物,所研究的微污染物以500 g/dm的浓度加入其中。对所选化合物在去离子水中的降解效果进行了比较。研究发现,光催化的效率在很大程度上取决于环境基质和处理后废水中化合物的物理化学性质。仅含无机物的合成出水的降解效率最高。辐照60分钟后,双酚A和17 -乙基雌二醇的降解率超过90%,17 -雌二醇被完全分解。观察到的现象可归因于称为敏化光催化的过程,这是由合成废水中存在的无机物实现的。同时含有无机物和有机物的合成出水没有出现这种现象,而且对微污染物的降解效率较低。有关化合物在去离子水中分解的结果也证实了这些观察结果。为了描述光催化氧化过程,采用Langmuir-Hinshelwood动力学模型确定了光催化氧化反应的速率常数和降解半衰期。
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Comparative studies on decomposition of selected estrogens and xenoestrogens by photocatalysis processes
This study addressed the degradation efficiency of three different compounds belonging to the group of endocrine disrupting compounds (EDCs), namely 17 -estradiol (E2), 17 -ethinyl estradiol (EE2), and bisphenol A (BPA) in the photocatalysis process (UV/TiO2). The subject of the study was a synthetic municipal waste water treatment plant effluent containing inorganic and optionally organic substances and to which the investigated micropollutants were added at a concentration of 500 g/dm. The obtained results were compared in terms of the degradation of the selected compounds in deionized water. It was found that the efficiency of the photocatalysis depends significantly both on the environmental matrix and physico-chemical properties of the compounds present in the treated waste water. The highest degradation efficiency was observed for the synthetic effluent that contained only inorganic substances. The degradation of bisphenol A and 17 -ethinyl estradiol exceeded 90 % (after 60-minute irradiation) and 17 -estradiol was decomposed completely. The observed phenomenon can be attributed to the process termed as sensitized photocatalysis, which was enabled by inorganic substances present in the synthetic waste water. This phenomenon was not observed for the synthetic effluent that contained both inorganic and organic substances, and moreover the degradation efficiency of the micropollutans was lower. These observations were also confirmed by the results regarding the decomposition of the compounds in deionized water. In order to describe the course of photocatalytic oxidation reaction rate constants were determined as well as degradation half-lives using the Langmuir-Hinshelwood kinetic model.
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