催化作用
罗丹明B
化学
氧化剂
X射线光电子能谱
无机化学
铜
傅里叶变换红外光谱
浸出(土壤学)
选择性催化还原
多相催化
碱金属
激进的
水溶液中的金属离子
核化学
金属
光催化
化学工程
有机化学
土壤科学
土壤水分
工程类
环境科学
作者
Ziyu Yao,Guangwu ZHU,Tianliang Lu,Yuzhong Zhan
摘要
Abstract Using the bulk g-C3N4 as a precursor, four g-C3N4 nanosheets were further prepared by ultrasonic, thermal, acid, and alkali exfoliation. The structures of these materials were characterized by various techniques such as X-ray powder diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, energy dispersive X-ray spectroscopy, transmission electron microscopy, and X-ray photoelectron spectroscopy. The synergistical Fenton catalysis of these materials with Cu2+ was evaluated by using rhodamine B as a simulated organic pollutant. The results showed that there existed a significant synergistical Fenton catalysis between Cu2+ and g-C3N4. This synergistic effect can be observed even when the concentration of Cu2+ was as low as 0.064 mg L−1. The properties of g-C3N4 strongly influenced the catalytic activity of the Cu2+/g-C3N4 system. The coexistent of Cu2+ and the alkali exfoliated g-C3N4 showed the best catalytic activity. Hydroxyl radicals as oxidizing species were confirmed in the Cu2+/g-C3N4 system by electron paramagnetic resonance spectra. The synergistic catalysis may be attributed to the easier reduction of Cu2+ adsorbed on the g-C3N4. This study provided an excellent Fenton catalytic system, and partly solved the rapid deactivation of heterogeneous Fenton catalysts caused by the leaching of metal ions.
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