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焦化场地土壤中甲苯的特殊衰减。

Peculiar attenuation of soil toluene at contaminated coking sites.

机构信息

National Engineering Research Centre of Urban Environmental Pollution Control, Beijing Key Laboratory for Risk Modeling and Remediation of Contaminated Sites, Beijing Municipal Research Institute of Environmental Protection, No. 59 Beiyingfang Middle Street, Xicheng District, 100037, Beijing, PR China.

National Engineering Research Centre of Urban Environmental Pollution Control, Beijing Key Laboratory for Risk Modeling and Remediation of Contaminated Sites, Beijing Municipal Research Institute of Environmental Protection, No. 59 Beiyingfang Middle Street, Xicheng District, 100037, Beijing, PR China; Nanjing Institute of Environmental Sciences, Ministry of Ecology and Environmental of the People's Republic of China, No. 8 Jiangwangmiao Street, 210042, Nanjing, PR China.

出版信息

Chemosphere. 2020 Sep;255:126957. doi: 10.1016/j.chemosphere.2020.126957. Epub 2020 May 5.

Abstract

In the soil of contaminated coking sites, polycyclic aromatic hydrocarbons (PAHs) and benzene, toluene, ethylbenzene and xylene (BTEX) are typical indicator compounds. Generally, PAHs are enriched in the topsoil layer. BTEX, with higher water solubilities and lower organic carbon-water partitioning coefficients (K), are distributed deeper than PAHs. However, current models have employed predictions using single compounds to mimic the migration of BTEX at contaminated coking sites. Such models have not considered the influence of the upper soil layer, where PAHs are enriched. An attempt to fill this gap was made by setting up a control soil column experiment in this study. One column was filled with undisturbed soil (column #1) and the other with PAH-contaminated soil (column #2) to simulate the theoretical and actual surface soil layers, respectively. The results showed that in column #2, the toluene gas concentration of the headspace and time required to reach steady state were notably greater than those in column #1. High-throughput sequencing revealed that there were large microbial community structure differences between the two soil columns throughout the experiment, while some genera that degrade toluene with high efficiency emerged noteworthily in column #2. This implied that the upper soil layer enriched with PAHs was conducive to the degradation of toluene vapor. Applying this finding to human health exposure assessment of toluene suggests that the potential exposure level should be reduced from the current predicted level given the unanticipated attenuation at contaminated coking sites.

摘要

在污染炼焦场地的土壤中,多环芳烃(PAHs)和苯、甲苯、乙苯和二甲苯(BTEX)是典型的指示化合物。一般来说,PAHs 富集在表土层。BTEX 具有较高的水溶性和较低的有机碳-水分配系数(K),分布深度比 PAHs 深。然而,目前的模型采用了使用单一化合物进行预测的方法来模拟污染炼焦场地中 BTEX 的迁移。这些模型没有考虑到 PAHs 富集的上层土壤的影响。本研究通过建立控制土壤柱实验试图弥补这一空白。一个柱子填充未扰动土壤(柱 #1),另一个柱子填充 PAH 污染土壤(柱 #2),分别模拟理论和实际的表土层。结果表明,在柱 #2 中,顶部空间的甲苯气体浓度和达到稳定状态所需的时间明显大于柱 #1。高通量测序结果表明,整个实验过程中,两个土壤柱之间的微生物群落结构存在显著差异,而在柱 #2 中,一些高效降解甲苯的属也引人注目地出现了。这意味着富含 PAHs 的上层土壤有利于甲苯蒸气的降解。将这一发现应用于甲苯对人体健康暴露的评估表明,鉴于污染炼焦场地中出现的意外衰减,潜在暴露水平应从当前预测水平降低。

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