Authors
Yuan Bai, Boxuan Wang, Xin Zhang, Zhihua Chen, Kai Jiang, Dapeng Wu
Published in
Bioresource technology. Pages 135547. Aug 01, 2026. Epub Aug 01, 2026.
Abstract
The accumulation of antibiotic fermentation residue (AFR) and pharmaceutical waste salt (WS) poses a severe disposal challenge. Herein, we report a WS-assisted co-pyrolysis strategy is proposed to convert these hazardous waste streams into an active material for hexavalent chromium (Cr(VI)) reduction. During pretreatment, the intrinsic osmotic stress of WS disrupts AFR microbial cells in AFR, thereby promoting deep dehydration. The subsequent thermal process effectively degrades residual antibiotics and antibiotic resistance genes. During co-pyrolysis, the inherent NaCl in WS acts as a mineral-phase regulator. The salt matrix promotes pore development in the carbon matrix, forming a hierarchical pore architecture. Concurrently, the salt matrix converts calcium-rich components into Ca5(PO4)3OH. These Ca5(PO4)3OH domains enrich CrO42- near Fe-containing redox sites, where Fe-mediated electron transfer drives the aqueous reduction of Cr(VI) to Cr(III). The synthesized composite achieves more than 90% reduction of low-concentration Cr(VI). Economic evaluation confirms the financial feasibility of this integrated protocol when avoided hazardous-waste disposal costs are considered. This integrated upcycling strategy mitigates pharmaceutical solid waste while producing functional biochar for environmental remediation.
PMID:
42542151
Bibliographic data and abstract were imported from PubMed on 02 Aug 2026.
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