A green strategy from waste red mud to Fe0-based biochar for sulfadiazine treatment by peroxydisulfate activation

生物炭 化学 过氧二硫酸盐 磺胺嘧啶 废物管理 过硫酸盐 激进的 零价铁 废水 降级(电信) 核化学 腐植酸 环境修复 热解 环境化学 吸附 有机化学 催化作用 生物化学 污染 工程类 电信 肥料 计算机科学 抗生素 生态学 生物
作者
Dongmei Ma,Jing Wang,Kun Feng,Bingfeng Liu,Guo-Jun Xie,Defeng Xing
出处
期刊:Chemical Engineering Journal [Elsevier]
卷期号:446: 136944-136944 被引量:23
标识
DOI:10.1016/j.cej.2022.136944
摘要

Zerovalent iron (Fe0)-based biochar (Fe0-BC) has attracted wide attention in activating persulfate to eliminate antibiotics. In this study, the waste red mud (RM) was successfully used as an iron precursor to prepare Fe0-BC (RMIS1:1) via co-pyrolysis strategy, which was confirmed with remarkable capacity in peroxydisulfate (PDS) activation. The removal efficiency of sulfadiazine (SDZ) was 99.7% in RMIS1:1/PDS system in 20 min, with kobs of 0.3001 min−1. Both free radicals (SO4−, OH, and O2−) and non-free radicals (1O2) were responsible for SDZ degradation, in which the SO4− and O2− played the dominant roles. Four SDZ degradation pathways were provided according to the intermediates identified by Q-TOF-MS. Furthermore, the ECOSAR prediction implied that the intermediates have less eco-toxicity than SDZ. Compared with PDS concentration and RMIS1:1 dosage, the initial SDZ concentration had stronger effect on its degradation. Co-existed Cl− slightly improved SDZ degradation rate, while other anions (NO3–/SO42−/HCO3–/CO32–) and humic acid exhibited different levels of inhibition on SDZ removal. Moreover, RMIS1:1/PDS maintained acceptable degradation ability for practical pharmaceutical wastewater. The electrical energy per mass of SDZ was about 2.24 kWh/(g·SDZ) by RMIS1:1/PDS, lower than that produced in any other advanced oxidation processes that have been reported so far. In summary, this study reported a green strategy for Fe0-BC preparation from RM, which was valuable for both waste resource recycling and environmental remediation.
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