过氧二硫酸盐
过硫酸盐
生物炭
化学
电子转移
咔唑
热解
电化学
降级(电信)
环境修复
地下水修复
高级氧化法
无机化学
猝灭(荧光)
质子化
水处理
环境化学
光化学
碳纤维
电子受体
生物量(生态学)
密度泛函理论
二苯并呋喃
兴奋剂
纳米材料
化学工程
尿素
水溶液
碳化
作者
Hao Dong,Nan Zhao,Qianting Xu,Ye Xiao,Weihua Zhang,Rongliang Qiu
标识
DOI:10.1016/j.jclepro.2026.147913
摘要
Carbazole (CBZ) is a ubiquitous and toxic N-heterocyclic contaminant in water and soil, posing substantial environmental risks. Current remediation strategies for CBZ struggle with low efficiency, high energy consumption, or strict operational conditions, making persulfate-based advanced oxidation a promising alternative. Herein, we synthesized a series of urea-tailored biochars (UBCs) via low-temperature co-pyrolysis. Among them, UBC5 featuring an extremely high N content (21.4%) showed optimal peroxydisulfate (PDS) activation for CBZ degradation. The UBC5/PDS system achieved ∼90% CBZ removal within 1 h across pH 3-9, and exhibited strong resistance to inorganic anions (Cl − , SO 4 2− , H 2 PO 4 − ) and humic acid. Furthermore, the system effectively degraded CBZ in soil (71-82% within 1 h), with residual concentrations falling below safety thresholds for industrial land after 12 h. Quenching experiments, electron paramagnetic resonance, and electrochemical analyses revealed a non-radical degradation pathway: UBC5-PDS∗ mediated electron transfer, with a minor contribution from 1 O 2 . Characterizations and density functional theory calculations elucidated a unique “in-plane to out-of-plane electron transfer” mechanism. The degradation intermediates exhibited reduced toxicity, with negligible adverse effects on soybean growth. Notably, UBC5 has lower production cost ($9.52 kg −1 ) and carbon emissions (18.38 kg CO 2 e kg −1 ) than typical activators. This study provides new insight for the design of carbon-based persulfate activators and an efficient, sustainable approach for the remediation of CBZ-contaminated water and soil.
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