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城市生活垃圾焚烧厂附近土壤中多氯二苯并对二恶英和多氯二苯并呋喃的大气沉降。

Atmospheric deposition of polychlorinated dibenzo-p-dioxins and dibenzofurans on the soils in the vicinity of municipal solid waste incinerators.

机构信息

Department of Environmental Engineering, National Cheng Kung University, Tainan, Taiwan.

出版信息

J Environ Sci Health A Tox Hazard Subst Environ Eng. 2009 Nov;44(13):1327-34. doi: 10.1080/10934520903213020.

DOI:10.1080/10934520903213020
PMID:20183489
Abstract

This study focuses on the atmospheric deposition of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) on the soils in the vicinity of two municipal solid waste incinerators (MSWIs), which were located in the Gangshan (GS) and the Renwu (RW) Townships of southern Taiwan. PCDD/Fs in the soils were sampled simultaneously with those in the ambient air and analyzed for 17 2,3,7,8-substituted PCDD/Fs. The results show that the mean contents of PCDD/Fs in the soils near MSWI-GS and MSWI-RW were 2.65 and 1.20 ng I-TEQ/kg dry weight, respectively. Annual wet deposition fluxes of total PCDD/Fs were 119 and 113 ng/m(2)-year in the ambient air near MSWI-GS and MSWI-RW, respectively. The results obtained in this study are much higher than those estimated for the Atlantic Ocean, where the average wet deposition was only 45 ng/m(2)-year. The annual dry deposition fluxes accounted for 58.2 and 66.7%, respectively, indicating that dry deposition was more dominant than wet deposition in the atmospheric deposition processes. The congener profiles of 17 2,3,7,8-substituted PCDD/Fs showed that OCDD dominates in the soils. The contributions of OCDD in the soils near MSWI-GS and MSWI-RW were 73.4 and 67.1%, respectively, while they were only 41.4 and 31.2% in the atmospheric deposition, respectively. These results imply that OCDD is more persistent in the environment than other congeners. The results of the present study strongly suggest that exposure to PCDD/Fs in these areas should be reduced.

摘要

本研究聚焦于两座都市固体废物焚化炉(MSWI)附近土壤中多氯二苯并对二恶英和多氯二苯并呋喃(PCDD/Fs)的大气沉降。同时对土壤和环境空气中的 PCDD/Fs 进行采样,并对 17 种 2,3,7,8-取代的 PCDD/Fs 进行分析。结果表明,MSWI-GS 和 MSWI-RW 附近土壤中 PCDD/Fs 的平均含量分别为 2.65 和 1.20ng 毒性当量/kg 干重。在 MSWI-GS 和 MSWI-RW 附近环境空气中,总 PCDD/Fs 的年湿沉降通量分别为 119 和 113ng/m(2)-年。本研究结果明显高于大西洋的估计值,大西洋的平均湿沉降通量仅为 45ng/m(2)-年。年干沉降通量分别占 58.2%和 66.7%,表明干沉降在大气沉降过程中比湿沉降更为重要。17 种 2,3,7,8-取代的 PCDD/Fs 同系物的分布表明 OCDD 在土壤中占主导地位。MSWI-GS 和 MSWI-RW 附近土壤中 OCDD 的贡献率分别为 73.4%和 67.1%,而在大气沉降中,其贡献率分别为 41.4%和 31.2%。这些结果表明 OCDD 在环境中比其他同系物更持久。本研究结果强烈表明,应减少这些地区 PCDD/Fs 的暴露。

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