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Arsenic burden in e-waste recycling workers – A cross-sectional study at the Agbogbloshie e-waste recycling site, Ghana.
- Source :
-
Chemosphere . Dec2020, Vol. 261, pN.PAG-N.PAG. 1p. - Publication Year :
- 2020
-
Abstract
- The export of e-waste from industrialized to developing countries has led to the formation of a large-scale informal e-waste recycling sector in Accra, Ghana. During recycling processes, workers are exposed to several hazardous substances, such as heavy metals. As a common component of e-waste, inorganic arsenic can be released during e-waste recycling processes. The aim of this study was to assess the exposure to inorganic arsenic species in e-waste workers compared to a control group. N = 84 e-waste workers and n = 94 control subjects were included in this analysis. Inorganic arsenic species were determined in urine samples using HPLC-ICP-MS. E-waste workers showed higher median concentrations of As(III), As(V), MMA, DMA and the sum of inorganic arsenic in comparison to the control group. More than 80% of the e-waste workers exceeded the acceptable concentration (14 μg/L), which was significantly higher in comparison to the control group (70%). The tolerable concentration (40 μg/L) was exceeded in 17.2% of the participants, meaning a statistically relevant risk of developing cancer due to arsenic exposure throughout their (working) life. In conclusion, the exposure to inorganic arsenic is not only a problem of informal e-waste recycling, but a major public health concern that needs further investigation. • E-waste workers showed higher levels of inorganic arsenic compared to controls. • Burners had highest levels of inorganic arsenic in the e-waste group. • Inorganic arsenic concentrations in almost all workers exceeded the acceptable risk. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 00456535
- Volume :
- 261
- Database :
- Academic Search Index
- Journal :
- Chemosphere
- Publication Type :
- Academic Journal
- Accession number :
- 146562169
- Full Text :
- https://doi.org/10.1016/j.chemosphere.2020.127712