Moeckel Claudia, Breivik Knut, Nøst Therese Haugdahl, Sankoh Alhaji, Jones Kevin C, Sweetman Andrew
NILU - Norwegian Institute for Air Research, 2007 Kjeller, Norway; Stockholm University, 11418 Stockholm, Sweden.
NILU - Norwegian Institute for Air Research, 2007 Kjeller, Norway; University of Oslo, 0351 Oslo, Norway.
Environ Int. 2020 Apr;137:105563. doi: 10.1016/j.envint.2020.105563. Epub 2020 Feb 25.
Organic contaminants (polycyclic aromatic hydrocarbons (PAHs), polybrominated diphenyl ethers (PBDEs), polychlorinated biphenyls (PCBs), and chlorinated paraffins (CPs)) and heavy metals and metalloids (Ag, Cd, Co, Cr, Cu, Hg, Ni, Pb, Sb, Zn) were analysed in surface soil samples from the Agbogbloshie e-waste processing and dumping site in Accra (Ghana). In order to identify which of the pollutants are likely to be linked specifically to handling of e-waste, samples were also collected from the Kingtom general waste site in Freetown (Sierra Leone). The results were compared using principal component analyses (PCA). PBDE congeners found in technical octa-BDE mixtures, highly chlorinated PCBs and several heavy metals (Cu, Pb, Ni, Cd, Ag and Hg) showed elevated concentrations in the soils that are likely due to contamination by e-waste. PCAs associated those compounds with pyrogenic PAHs, suggesting that burning of e-waste, a common practice to isolate valuable metals, may cause this contamination. Moreover, other contamination pathways, especially incorporation of waste fragments into the soil, also appeared to play an important role in determining concentrations of some of the pollutants in the soil. Concentrations of several of these compounds were extremely high (especially PBDEs, heavy metals and SCCPs) and in some cases exceeded action guideline levels for soil. This indicates that exposure to these contaminants via the soil alone is potentially harmful to the recyclers and their families living on waste sites. Many organic contaminants and other exposure pathways such as inhalation are not yet included in such guidelines but may also be significant, given that deposition from the air following waste burning was identified as a major pollutant source.
对来自阿克拉(加纳)阿博布罗西电子垃圾处理和倾倒场的表层土壤样本中的有机污染物(多环芳烃(PAHs)、多溴二苯醚(PBDEs)、多氯联苯(PCBs)和氯化石蜡(CPs))以及重金属和类金属(银(Ag)、镉(Cd)、钴(Co)、铬(Cr)、铜(Cu)、汞(Hg)、镍(Ni)、铅(Pb)、锑(Sb)、锌(Zn))进行了分析。为了确定哪些污染物可能与电子垃圾处理有特定关联,还从弗里敦(塞拉利昂)的金托姆一般垃圾场采集了样本。使用主成分分析(PCA)对结果进行了比较。在工业八溴二苯醚混合物中发现的多溴二苯醚同系物、高氯多氯联苯以及几种重金属(铜(Cu)、铅(Pb)、镍(Ni)、镉(Cd)、银(Ag)和汞(Hg))在土壤中的浓度升高,这可能是由于电子垃圾污染所致。主成分分析将这些化合物与热解多环芳烃联系起来,表明焚烧电子垃圾(一种分离贵重金属的常见做法)可能导致这种污染。此外,其他污染途径,特别是将垃圾碎片混入土壤,似乎在确定土壤中某些污染物的浓度方面也发挥着重要作用。其中几种化合物的浓度极高(尤其是多溴二苯醚、重金属和短链氯化石蜡),在某些情况下超过了土壤行动指南水平。这表明仅通过土壤接触这些污染物就可能对生活在垃圾场的回收者及其家人有害。许多有机污染物和其他接触途径(如吸入)尚未纳入此类指南,但鉴于垃圾焚烧后空气中的沉积物被确定为主要污染源,这些途径可能也很重要。