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饮用水源中多环芳烃的直接光解。

Direct photolysis of polycyclic aromatic hydrocarbons in drinking water sources.

机构信息

Instituto de Biologia Experimental e Tecnológica, Av República, Qta do Marquês, EAN, 2784-505 Oeiras, Portugal.

出版信息

J Hazard Mater. 2011 Sep 15;192(3):1458-65. doi: 10.1016/j.jhazmat.2011.06.065. Epub 2011 Jun 30.

Abstract

The widely used low pressure lamps were tested in terms of their efficiency to degrade polycyclic aromatic hydrocarbons listed as priority pollutants by the European Water Framework Directive and the U.S. Environmental Protection Agency, in water matrices with very different compositions (laboratory grade water, groundwater, and surface water). Using a UV fluence of 1500 mJ/cm(2), anthracene and benzo(a)pyrene were efficiently degraded, with much higher percent removals obtained when present in groundwater (83-93%) compared to surface water (36-48%). The removal percentages obtained for fluoranthene were lower and ranged from 13 to 54% in the different water matrices tested. Several parameters that influence the direct photolysis of polycyclic aromatic hydrocarbons were determined and their photolysis by-products were identified by mass spectrometry. The formation of photolysis by-products was found to be highly dependent on the source waters tested.

摘要

广泛使用的低压灯在不同组成的水基质(实验室级水、地下水和地表水)中,根据它们降解被欧洲水框架指令和美国环境保护署列为优先污染物的多环芳烃的效率进行了测试。使用 1500 mJ/cm(2) 的紫外线辐照度,蒽和苯并(a)芘被有效降解,当存在于地下水(83-93%)时,去除率比地表水(36-48%)高得多。在所测试的不同水基质中,荧蒽的去除率较低,范围为 13%至 54%。确定了影响多环芳烃直接光解的几个参数,并通过质谱法鉴定了它们的光解副产物。发现光解副产物的形成高度依赖于所测试的水源。

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