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The visible light photo-Fenton-like catalytic performance of BiFeO3 nanoparticles was investigated using Methyl Violet (MV), Rhodamine B (RhB) and phenol as probes. Under optimum conditions, the pseudo first-order rate constant (k) was determined to be 2.21×10-2, 5.56×10-2 and 2.01×10-2 min-1 for the degradation of MV (30 μmol/L), RhB (10 μmol/L) and phenol (3 mmol/L), respectively, in the BiFeO3-H2O2-visible light (Vis) system. The introduction of visible light irradiation increased the k values of MV, RhB and phenol degradation 3.47, 1.95 and 2.07 times in comparison with those in dark. Generally, the k values in the BiFeO3-H2O2-Vis system were accelerated by increasing BiFeO3 load and H2O2 concentration, but decreased with increasing initial pollutant concentration. To further enhance the degradation of pollutants at high concentrations, BiFeO3 was modified with the addition of surface modifiers. The addition of ethylenediamineteraacetic acid (EDTA, 0.4 mmol/L) increased the k value of MV degradation (60 μmol/L) from 1.01×10-2 min-1 in the BiFeO3-H2O2-Vis system to 1.30 min-1 in the EDTA-BiFeO3-H2O2-Vis system by a factor of 128. This suggests that in situ surface modification can enable BiFeO3 nano-particles to be a promising visible light photo-Fenton-like catalyst for the degradation of organic pollutants. 相似文献
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通过对成都地区典型移动通信基站的电磁环境监测,分析了移动通信基站的电磁环境规律及程度,明确其产生电磁环境影响在10-2W/m2等级,满足国标公众照射限值0.4W/m2的要求,并提出移动通信基站选址需要考虑的问题。 相似文献
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-PbO2 electrodes were prepared by electro-deposition and characterized by scanning electron microscopy, X-ray diffraction, X-ray
photoelectron spectroscopy, and linear sweep voltammetry. We confirmed pure -PbO2 crystals were on the electrode and it had a high
oxygen evolution potential. The photoactivity and photoelectrochemical (PEC) properties of the -PbO2 electrode were investigated
under visible light irradiation ( > 420 nm) for the decolorization of Methylene Blue. Pseudo first-order kinetics parameter (Kapp) for
dye decolorization using the -PbO2 electrode achieved 6.71×10?4 min?1 under visible light irradiation, which indicated its excellent
visible light-induced photoactivity. The Kapp of the PEC process was as much as 1.41×10?3 min?1 and was 1.71 times that of visible light
irradiation or electrolysis even in the presence of the -PbO2 electrode. A significant synergetic effect was observed in the PEC system.
We also employed TiO2 modified -PbO2 electrodes in this test, which revealed that the TiO2 immobilized on the -PbO2 electrode
inhibited the visible light-induced PEC efficiency despite the amount of TiO2 used for electrode preparation. The -PbO2 electrode was
also superior to the dimensionally stable anode (Ti/Ru0:3Ti0:7O2) in visible light-induced photoactivity and PEC efficiency. 相似文献