生物炭
硫代硫酸盐
过硫酸盐
降级(电信)
激进的
化学
电子转移
猝灭(荧光)
氰化物
单线态氧
电子顺磁共振
光化学
核化学
无机化学
氧气
催化作用
有机化学
硫黄
计算机科学
荧光
热解
量子力学
物理
电信
核磁共振
作者
Chenfei Shi,Kai Hu,Liyao Nie,Haorui Wang,Lili Ma,Qiong Du,Guoxiang Wang
标识
DOI:10.1016/j.inoche.2022.110160
摘要
• Acetaminophen was rapidly degraded in persulfate/P-doped biochar/thiosulfate system. • A synergistic effect existed among persulfate, p-doped biochar and thiosulfate. • Electron transfer could be responsible for the degradation of acetaminophen. • The system maintained high removal efficiency in the water from difference sources. In the study, p-doped biochar (PBC) was prepared by the pyrolysis of H 3 PO 4 -impregnated cyanobacteria and used together with thiosulfate (TS) to activate persulfate (PS) for the degradation of acetaminophen (ACP). The biochar was characterized and the results showed that H 3 PO 4 treatment had a pronounced effect on the surface structure and chemical composition of biochar. ACP (0.05 mmol/L) could be completely removed within 90 min under the optimal conditions: 2.0 mmo/L of PS, 0.1 g/L of PBC and 2.0 mmol/L of TS. A synergistic effect existed among PS, PBC and TS. The PS/PBC/TS system maintained high removal efficiency for ACP in the water from difference sources and Cl - (< 2.0 mmol/L) had little effect on it. Quenching experiments, electron paramagnetic resonance measurements and ion analysis revealed that free radicals (SO 4 • − and •OH) and singlet oxygen were not the main reactive species and biochar-mediated electron transfer could be responsible for the degradation of ACP. This work provides a novel method for the degradation of pharmaceutical and personal care products through non-radical pathway and will be benefit for the development of efficient persulfate-based advanced oxidation processes.
科研通智能强力驱动
Strongly Powered by AbleSci AI