Zero-valent iron and biochar composite with high specific surface area via K2FeO4 fabrication enhances sulfadiazine removal by persulfate activation

生物炭 零价铁 磺胺嘧啶 过硫酸盐 化学 降级(电信) 过氧二硫酸盐 吸附 化学工程 热解 无机化学 核化学 催化作用 有机化学 生物化学 工程类 电信 抗生素 计算机科学
作者
Dongmei Ma,Yang Yang,Bing-Feng Liu,Guo-Jun Xie,Chuan Chen,Nan-Qi Ren,Defeng Xing
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:408: 127992-127992 被引量:170
标识
DOI:10.1016/j.cej.2020.127992
摘要

Zero-valent iron and biochar composite (ZVI/BC) is a prospective catalyst for activating persulfate and specific surface area (SSA) of ZVI/BC is one of the most important factors affecting its efficacy in the removal of environmental contaminants. However, the green fabrication of ZVI/BC with large SSA remains a challenge. In this study, ZVI/BC with a highly porous structure and large SSA fabricated by co-pyrolysis of K2FeO4 and bamboo was prepared and characterized. The large SSA stemmed from the catalytic and corrosive functions of K and the oxidation of K2FeO4 onto bamboo. ZVI/BC fabricated with 0.05 mol/L K2FeO4 (BC-Fe0.05) showed optimal sulfadiazine (SDZ) removal performance in the peroxydisulfate (PDS) activation system with complete removal after 10 min, as it showed the highest adsorptive ability of SDZ. Moreover, BC-Fe0.05 was able to remain stable after four cycles or 80 days of storage. Higher temperature, lower pH, and Cl− were beneficial to SDZ removal efficiency, whereas CO32– and HPO42− had inhibitory effects. Non-radical species (1O2) and radical species (SO4−, OH, and O2−) both contributed to SDZ degradation, and 1O2 was the most important reactive oxygen species. Four degradation pathways were proposed based on ten identified intermediates. Potential eco-toxicity analysis by ECOSAR suggested that most intermediates were less toxic than their parent compound. Overall, this study describes a green fabrication method for ZVI/BC with large SSA using K2FeO4 as the iron precursor. Generally, ZVI/BC with large SSA is an effective catalyst for activating persulfate to degrade antibiotics.
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