Environmental Chemistry
Polybrominated diphenyl ethers in surface soils from e-waste recycling areas and industrial areas in South China: Concentration levels, congener profile, and inventory
Article first published online: 12 OCT 2011
DOI: 10.1002/etc.668
Copyright © 2011 SETAC
Additional Information
How to Cite
Gao, S., Hong, J., Yu, Z., Wang, J., Yang, G., Sheng, G. and Fu, J. (2011), Polybrominated diphenyl ethers in surface soils from e-waste recycling areas and industrial areas in South China: Concentration levels, congener profile, and inventory. Environmental Toxicology and Chemistry, 30: 2688–2696. doi: 10.1002/etc.668
Publication History
- Issue published online: 10 NOV 2011
- Article first published online: 12 OCT 2011
- Accepted manuscript online: 31 AUG 2011 10:20PM EST
- Manuscript Accepted: 14 AUG 2011
- Manuscript Revised: 9 MAY 2011
- Manuscript Received: 4 MAR 2011
Vol. 31, Issue 4, 928, Article first published online: 17 MAR 2012
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Keywords:
- Polybrominated diphenyl ethers;
- E-waste;
- Concentration level;
- Congener profile;
- Mass inventory
Abstract
Polybrominated diphenyl ethers (PBDEs) were determined in 60 surface soils from two e-waste recycling sites (Qingyuan and Guiyu, China) and their surrounding areas to assess the extent and influence of PBDEs from e-waste recycling sites on the surrounding areas. A total of 32 surface soils from industrial areas in South China were also investigated for comparison. The mean concentrations of total PBDEs in the e-waste recycling sites of Guiyu and Qingyuan were 2,909 and 3,230 ng/g dry weight, respectively, whereas the PBDE concentrations decreased dramatically (1–2 orders of magnitude) with increasing distance from the recycling site, suggesting that the e-waste recycling activities were the major source of PBDEs in the surrounding areas. Decabromodiphenyl ethers accounted for 77.0 to 85.8% of total PBDEs in e-waste recycling areas, whereas it accounted for 90.2% in industrial areas. Principal component analysis showed that the major source of PBDEs in e-waste recycling areas were a combination of penta-, octa-, and deca-BDE commercial formulations, whereas deca-BDE commercial formulations were the major source of PBDE congeners in industrial areas. The inventories of PBDEs gave preliminary estimates of 6.22 tons and 13.4 tons for the e-waste recycling areas and industrial areas. The results suggested that significantly higher PBDEs in the e-waste recycling sites have already affected surrounding areas negatively within a relatively large distance. Because of the environmental persistence, bioaccumulation, and toxicity of PBDEs, improving the recycling techniques employed at such facilities and developing e-waste management policies are necessary. Environ. Toxicol. Chem. 2011;30:2688–2696. © 2011 SETAC

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