Centre for Biogeochemistry in the Anthropocene, Department of Chemistry, University of Oslo, P.O. Box 1033, 0315 Oslo, Norway; NILU-Norwegian Institute for Air Research, P.O. Box 100, 2027 Kjeller, Norway.
Centre for Biogeochemistry in the Anthropocene, Department of Chemistry, University of Oslo, P.O. Box 1033, 0315 Oslo, Norway.
Environ Pollut. 2022 Jan 1;292(Pt A):118298. doi: 10.1016/j.envpol.2021.118298. Epub 2021 Oct 6.
There are large knowledge gaps concerning environmental levels and fate of many organic pollutants, particularly for chemicals of emerging concern in tropical regions of the Global South. In this study, we investigated the levels of chlorinated paraffins (CPs) and dechloranes in air and soil in rural, suburban, and urban regions in and around Dar es Salaam, Tanzania. Samples were also collected near the city's main municipal waste dumpsite and an electronic waste (e-waste) handling facility. In passive air samples, short chain CPs (SCCPs) dominated, with an average estimated concentration of 22 ng/m, while medium chain CPs (MCCPs) had an average estimated concentration of 9 ng/m. The average estimated air concentration of ∑dechloranes (Dechlorane Plus (DP) + Dechlorane 602 + Dechlorane 603) was three to four orders of magnitudes lower, 2 pg/m. In soil samples, MCCPs dominated with an average concentration of 640 ng/g dw, followed by SCCPs with an average concentration of 330 ng/g dw, and ∑dechloranes with an average concentration of 0.9 ng/g dw. In both air and soil, DP was the dominating dechlorane compound. Urban pulses were observed for CPs and dechloranes in air and soil. CPs were in addition found in elevated levels at the municipal waste dumpsite and the e-waste handling facility, while DPs were found in elevated levels at the e-waste handling facility. This suggests that waste handling sites represent important emission sources for these pollutants. Investigations into seasonal trends and environmental fate of CPs and dechloranes showed that monsoonal rain patterns play a major role in governing air concentrations and mobility, particularly for the less volatile MCCPs and dechloranes. This study is the first to report levels of CPs in air from sub-Saharan Africa, and DP, Dechlorane 602, and Dechlorane 603 in soil from sub-Saharan Africa.
关于许多有机污染物的环境水平和归宿,特别是在全球南方热带地区的新出现的关切化学品方面,存在着很大的知识差距。在这项研究中,我们调查了达累斯萨拉姆及其周边农村、郊区和城市地区空气中和土壤中氯化石蜡(CPs)和脱氯烷的水平。还在该市主要的城市垃圾填埋场和电子废物(电子废物)处理设施附近采集了样本。在被动空气样本中,短链氯化石蜡(SCCPs)占主导地位,平均估计浓度为 22ng/m,而中链氯化石蜡(MCCPs)的平均估计浓度为 9ng/m。∑脱氯烷(氯化石蜡 602 与氯化石蜡 603 的混合物(DP)+氯化石蜡 602+氯化石蜡 603)的平均估计空气浓度低三个到四个数量级,为 2pg/m。在土壤样本中,MCCPs 占主导地位,平均浓度为 640ng/g dw,其次是 SCCPs,平均浓度为 330ng/g dw,∑脱氯烷的平均浓度为 0.9ng/g dw。在空气和土壤中,DP 是占主导地位的脱氯烷化合物。在空气和土壤中都观察到 CP 和脱氯烷的城市脉冲。在城市垃圾填埋场和电子废物处理设施中还发现 CP 含量升高,而在电子废物处理设施中则发现 DP 含量升高。这表明废物处理场是这些污染物的重要排放源。对 CP 和脱氯烷的季节性趋势和环境归宿的调查表明,季风降雨模式在控制空气浓度和流动性方面起着重要作用,特别是对挥发性较低的 MCCPs 和脱氯烷。本研究首次报道了撒哈拉以南非洲空气中 CP 的水平,以及撒哈拉以南非洲土壤中 DP、氯化石蜡 602 和氯化石蜡 603 的水平。