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Updated: Jan 24, 2026

Assessment of Waste-Derived Biochars on the Health and Biological Activity of Soil
Published on: October 10, 2025
Climatic and soil-mineralogical controls on the mobility of trace metal contamination released by informal electronic
Lonia R Friedlander1, Noam Weisbrod2, Yaakov J Garb3
1The Swiss Institute for Dryland Environmental and Energy Research, The Jacob Blaustein Institutes for Desert Research, Ben-Gurion University of the Negev, Midreshet Ben-Gurion, Sde Boqer, 8499000, Israel.
Abstract:
Informal e-waste processing is a growing global problem. Local climate and mineralogical factors strongly control the chemical lability and dispersal of trace metals from informal e-waste processing. Previous work on e-waste contamination primarily focused on well-known sites in similar climates. Our exploratory analysis of a long-term (since 2008) e-waste incineration site in East Jerusalem demonstrated the ways in which local factors combined to uniquely control trace metal contaminant mobility. Our results suggest that the combination of e-waste processing methods, climate, and mineralogy at this site generated a geopolymer-like material combining ash from e-waste incineration and mountain rendzina soil. This material strongly sorbs trace metal contaminants. We measured the concentrations of: Cu, Fe, Mn, Pb, and Zn at 29 locations around and within the burn site. Samples collected less than 10 m from the edge of the incineration area had trace metal concentrations below the United States Environmental Protection Agency (U.S. E.P.A.) screening levels for residential soil. Sequential extraction showed that ∼50-80% of the total mobilized Pb was released from the residual solid fraction, suggesting strong sorption or incorporation into soil components. Large differences in the measured average specific surface areas (SSA) of uncontaminated (26.18 m2/g) and contaminated (4.48 m2/g) samples, despite comparable mineralogy by XRD, suggested the production of a geopolymer-like material. This was supported by close similarities between the SSA values of contaminated samples and those measured for geopolymer materials synthesized in the lab using kaolinite clay and fly ash (e.g., 4.9 m2/g).
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