碳热反应
X射线光电子能谱
催化作用
零价铁
过硫酸盐
扫描电子显微镜
烧结
材料科学
核化学
环丙沙星
降级(电信)
化学
化学工程
冶金
复合材料
有机化学
吸附
工程类
电信
抗生素
生物化学
计算机科学
碳化物
作者
Yufeng Du,Min Dai,Iffat Naz,Xiang Hao,Xixi Wei,Rong Rong,Changsheng Peng,Imran Ali
标识
DOI:10.1016/j.seppur.2021.119201
摘要
In the present research, zero-valent iron (ZVI) was synthesized by carbothermal reduction method and its formation mechanism was studied. The obtained material ([email protected]) was applied as a persulfate (PS) catalyst for ciprofloxacin degradation. Further, Scanning Electron Microscopy (SEM) of [email protected] has shown that the crystal shape of Fe2O3 changed with the increase in temperature, and also revealed the spherical morphology of ZVI. X-ray Diffraction (XRD) further verified the process of conversion of Fe2O3 to Fe3O4 and then to ZVI. X-ray Photoelectron Spectroscopy (XPS) revealed that the change of iron valence state during the conversion process and the peak area of Fe2+ increased with sintering temperature. The effect of experimental parameters including pH, [email protected] dosage, PS concentration and temperature on ciprofloxacin degradation, were thoroughly investigated. The results illustrated that the [email protected] has excellent catalytic performance and can remove 90.78% of ciprofloxacin within 120 min. Free radical quenching experiments confirmed that the reaction of ciprofloxacin with ∙OH and SO4∙- mainly occurs on the [email protected] surface. Based on the different experiments, it was proposed that degradation mechanism of ciprofloxacin via [email protected] includes three aspects. Thus, it was found that carbothermal synthesis of [email protected] is cost effective and potential technology for ciprofloxacin remediation.
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