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受再生水灌溉的土壤中 PPCPs 的归趋和迁移。

Fates and transport of PPCPs in soil receiving reclaimed water irrigation.

机构信息

State Key Laboratory for Urban and Regional Ecology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China.

出版信息

Chemosphere. 2013 Nov;93(10):2621-30. doi: 10.1016/j.chemosphere.2013.09.088. Epub 2013 Oct 20.

Abstract

Fates and transport of 9 commonly found PPCPs of the reclaimed water were simulated based on the HYDRUS-1D software that was validated with data generated from field experiments. Under the default scenario in which the model parameters and input data represented the typical conditions of turf grass irrigation in southern California, the adsorption, degradation, and volatilization of clofibric acid, ibuprofen, 4-tert-octylphenol, 4-n-nonylphenol, naproxen, triclosan, diclofenac sodium, bisphenol A and estrone in the receiving soils were tracked for 10 years. At the end, their accumulations in the 90 cm soil profile varied from less than 1 ng g(-1) to about 140 ng g(-1) and their concentrations in the drainage water in the 90 cm soil depth varied from nil to μg L(-1) levels. The adsorption and microbial degradation processes interacted to contain the PPCPs entirely within surface 40 cm of the soil profiles. Leaching and volatilization were not significant processes governing the PPCPs in the soils. The extent of accumulations in the soils did not appear to produce undue ecological risks to the soil biota. PPCPs did not represent any potential environmental harm in reclaimed water irrigation.

摘要

基于 HYDRUS-1D 软件模拟了再生水中 9 种常见 PPCPs 的命运和迁移,该软件已通过野外实验生成的数据进行了验证。在默认情况下,模型参数和输入数据代表了南加州草坪灌溉的典型条件,在这种情况下,对土壤中氯菲酸、布洛芬、4-叔辛基苯酚、4-壬基苯酚、萘普生、三氯生、双氯芬酸钠、双酚 A 和雌酮的吸附、降解和挥发进行了 10 年的跟踪。最后,它们在 90 cm 土壤剖面中的积累量从小于 1ng/g 到约 140ng/g 不等,在 90cm 土壤深度的排水水中的浓度从无到μg/L 不等。吸附和微生物降解过程相互作用,将 PPCPs 完全限制在土壤剖面的表面 40cm 范围内。淋溶和挥发不是控制土壤中 PPCPs 的重要过程。在土壤中的积累程度似乎不会对土壤生物群造成不当的生态风险。PPCPs 在再生水灌溉中不会造成任何潜在的环境危害。

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