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Upcycling waste sericin into Fe3O4-anchored N-doped biochar for efficient peroxymonosulfate activation toward azo dye degradation

Journal 2026 · IF 8.2 · 发表于 2026 年 7 月 22 日
作者: Licong Xu,Cunxu Gong,Minghua Wu,Deyou Yu
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摘要

Waste sericin was valorized into Fe 3 O 4 / N -doped porous biochar Fenton-like catalyst. • Molecular coordination enabled uniform dispersion of active Fe 3 O 4 nanoparticles. • 0.1Fe-NC degraded 99.3% AO-7 with kobs of 0.266 min −1 via PMS activation. • Multiple ROS including Fe(IV)=O and 1 O 2 dominated the reaction. • Packed-bed continuous-flow operation kept >98% AO-7 removal for 720 min. Developing sustainable catalysts from waste biomass for advanced oxidation processes is highly desirable for wastewater treatment. Herein, a waste-to-resource strategy was proposed to upcycle silk-industry waste sericin into Fe 3 O 4 -anchored N -doped porous biochar Fenton-like catalysts (Fe-NC) for peroxymonosulfate (PMS) activation. Distinct from conventional biomass-derived Fe/carbon catalysts that often require external nitrogen dopants or post-loading of metal species, sericin served simultaneously as a carbon source, intrinsic nitrogen precursor, and Fe 3+ -binding biopolymer, enabling the coordination-assisted formation of Fe 3 O 4 / N -doped carbon interfacial active sites after controlled pyrolysis. The optimized 0.1Fe-NC possessed a high specific surface area of 477.9 m 2 g −1 and uniformly dispersed Fe 3 O 4 nanoparticles, enabling rapid removal of Acid Orange 7 (AO-7) over a wide pH range of 4–11. Nearly complete degradation of AO-7 (99.3%) was achieved within 30 min, with a pseudo-first-order rate constant ( k obs ) of 0.266 min −1 . Mechanistic investigations revealed that multiple reactive oxygen species, including Fe(IV)=O, SO 4 -, OH, and 1 O 2 , jointly contributed to pollutant degradation. In addition, the catalyst exhibited excellent magnetic recoverability and stability, maintaining 89.7% removal efficiency after five cycles. Continuous-flow experiments further demonstrated stable performance (>98% removal for 720 min), highlighting its practical applicability. This work provides a sustainable strategy for converting protein-rich sericin waste into efficient Fe-based biochar catalysts and offers insights into designing biomass-derived PMS activation systems with integrated heteroatom doping, metal anchoring, and interfacial electron-transfer regulation. Download: Download high-res image (166KB) Download: Download full-size image

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