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土壤中14C-双酚A的归宿

Fate of 14C-bisphenol A in soils.

作者信息

Fent Gunnar, Hein Werner J, Moendel Martin J, Kubiak Roland

机构信息

Department of Ecochemistry, State Education and Research Center Neustadt, Breitenweg 71, 67435, Neustadt, Germany.

出版信息

Chemosphere. 2003 Jun;51(8):735-46. doi: 10.1016/S0045-6535(03)00100-0.

Abstract

Bisphenol A (BPA; 2,2-(4,4(')-dihydroxydiphenyl)propane) is predominantly used as an intermediate in the production of polycarbonate plastics and epoxy resins. Traces of BPA released into the environment can reach the soil via application of sewage sludge from wastewater treatment systems that receive wastewaters containing BPA, or from leachate from uncontrolled landfills. The biodegradability of BPA has been previously investigated in several studies designed to simulate surface waters and biological wastewater treatment systems. However, there is little information available about the fate of BPA in soil. Therefore, laboratory soil degradation and batch adsorption studies were conducted with 14C-BPA and four soils according to international guidelines. The soils represented a broad range of physico-chemical properties. An important result of the degradation study was that, independent of the soil type, 14C-BPA was rapidly dissipated and not detectable in soil extracts following 3 days of incubation. Based on this result, a dissipation half-life of less than 3 days was estimated. The major route of dissipation of 14C-BPA in soil was the formation of bound residues that could not be recovered by exhaustive Soxhlet extraction. 14C-BPA was also shown to be transiently converted to up to five metabolites, but within 3 days, neither 14C-BPA nor 14C-metabolites were detectable in the soils. After 120 days incubation, significant amounts (up to 20% of the radioactivity applied) of the parent compound were recovered as 14CO(2). Soil adsorption experiments indicated that the distribution coefficients (K(oc)) were between 636 and 931, classifying BPA as having low mobility for all tested soils. From the results of this study, it was concluded that if BPA reaches the soil compartment, it is not expected to be stable, mobile, or bioavailable.

摘要

双酚A(BPA;2,2-(4,4′-二羟基二苯基)丙烷)主要用作生产聚碳酸酯塑料和环氧树脂的中间体。释放到环境中的微量双酚A可通过以下途径进入土壤:应用来自接收含双酚A废水的废水处理系统的污泥,或来自未加控制的垃圾填埋场的渗滤液。此前,已有多项研究对双酚A在模拟地表水和生物废水处理系统中的生物降解性进行了调查。然而,关于双酚A在土壤中的归宿,几乎没有可用信息。因此,根据国际准则,使用14C-双酚A和四种土壤进行了实验室土壤降解和批量吸附研究。这些土壤代表了广泛的物理化学性质。降解研究的一个重要结果是,无论土壤类型如何,在培养3天后,14C-双酚A迅速消散,在土壤提取物中无法检测到。基于这一结果,估计消散半衰期小于3天。14C-双酚A在土壤中的主要消散途径是形成不能通过索氏提取法完全回收的结合残留物。14C-双酚A还被证明会短暂转化为多达五种代谢物,但在3天内,土壤中既检测不到14C-双酚A,也检测不到14C-代谢物。培养120天后,回收了大量(高达所施加放射性的20%)母体化合物作为14CO₂。土壤吸附实验表明,分配系数(Koc)在636至931之间,这表明双酚A在所有测试土壤中的迁移性较低。从这项研究的结果得出结论,如果双酚A进入土壤环境,预计它不会稳定、可移动或具有生物可利用性。

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