催化作用
核化学
化学
激进的
盐酸四环素
X射线光电子能谱
复合数
光催化
多孔性
材料科学
打赌理论
比表面积
羟基自由基
化学工程
降级(电信)
四环素
有机化学
复合材料
电信
工程类
计算机科学
生物化学
抗生素
作者
Yixi Sun,Jiabin Zhou,Dan Liŭ,Xianjie Liu,Xi Li,Changhong Leng
标识
DOI:10.1016/j.jwpe.2021.102307
摘要
A simple solvothermal method was used to prepare poly-porous MnFe2O4/diatomite (MFD) with excellent catalytic performance. The characteristics of the prepared catalysts were examined by XRD, SEM, BET, XPS, UV-DRS, PL and NH3-TPD. BET analysis indicated that introduction of diatomite could increase the specific surface and porosity of the MFD. NH3-TPD studies clearly revealed that loading onto diatomite increased the availability of acid sites and surface hydroxyl groups in the composite materials. Under the combination of visible light and H2O2, the degradation effect of 80 mg/L 100 mL tetracycline hydrochloride (TC-HCl) reached 96.7% within 60 min at 0.1 g/L MFD and initial pH value, according to the experimental results. The proposed heterogeneous photo-Fenton system with MnFe2O4/diatomite showed an extremely wide pH range of 3–11 for TC-HCl degradation. At pH = 7, 91.8% of the TC-HCl (80 mg/L 100 mL) could be degraded within 60 min. In addition, the removal rate remained close to 90% after 60 min of irradiation at pH = 9 and 11. Free radical capture experiment showed that superoxide radicals (•O2−) and holes (h+) play a crucial role in the removal of TC-HCl. Moreover, the synergistic activation of H2O2 by Fe and Mn was confirmed to promote the degradation, leading to higher TC-HCl removal efficiency.
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