Enhanced Catalytic Activity of Bi 2 WO 6 for Organic Pollutants Degradation under the Synergism between Advanced Oxidative Processes and Visible Light Irradiation

被引:0
|
作者
Wang, Yuanqing [1 ]
Pan, Yusong [1 ]
Zhu, Hongwu [1 ]
Xiang, Yanlei [1 ]
Han, Rong [1 ]
Huang, Run [1 ]
Du, Chao [1 ]
Pan, Chengling [1 ]
机构
[1] Anhui Univ Sci & Technol, Sch Mat Sci & Engn, Huainan 232001, Anhui, Peoples R China
关键词
Photocatalysis; Advanced oxidation processes; Bi; 2; WO; 6; Peroxymonosulfate; Rhodamine B; HETEROGENEOUS ACTIVATION; BISMUTH TUNGSTATE; BISPHENOL-A; PEROXYMONOSULFATE; PERSULFATE; INSIGHTS; G-C3N4;
D O I
10.3866/PKU.WHXB202304050
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Environmental problems have become more and more serious with the continuous development of industrialized society. Especially, the problem of industrial wastewater has been a hot research issue in the field of catalytic degradation. Coupling photocatalysis and advanced oxidation processes (AOPs) is considered to be an efficient organic pollutant degradation technology due to its high efficiency, non -selectivity, and mild treatment conditions. In this article, the authors focused on the synthesis and characterization of Bismuth tungstate (Bi 2 WO 6 ) nanoflowers, which were prepared using a straightforward hydrothermal method in the presence of cetyltrimethylammonium bromide (CTAB) surfactant. To investigate the micro -morphology, crystal phase, surface chemical element states, and optical characteristics of the Bi 2 WO 6 nanoflowers, various methods such as X-ray diffraction (XRD), Fourier transform infrared (FTIR), scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray photoelectron spectroscopy (XPS), and diffuse reflection spectroscopy (DRS) were used. The catalytic performance of the Bi 2 WO 6 nanoflowers was then investigated for degrading organic pollutants under different catalytic systems. The removal efficiency of Rhodamine B (RhB) was up to 96.39% within 40 min under vis/ potassium monopersulfate triple salt (PMS)/ Bi 2 WO 6 system, which is obviously superior to that in both PMS/ Bi 2 WO 6 (38.77% in 40 min) and vis/Bi 2 WO 6 (31.82% in 40 min) systems, indicating that synergistic effects between visible -light irradiation and PMS accelerated the catalytic activity of Bi 2 WO 6 on the RhB degradation. The researchers also investigated the effect of ambient conditions on the catalytic performance of the systems, such as catalyst dosage, PMS concentration, pH value, and ion concentration. Interestingly, the vis/PMS/Bi 2 WO 6 system demonstrated high removal efficiency (up to 90%) despite changes in these parameters. However, the catalytic degradation rate ( k ) was influenced by these parameters in this system. Conversely, the environmental parameters have obvious influence on the catalytic degradation rate ( k ) under vis/PMS/ Bi 2 WO 6 system. The results showed that when the catalyst dosage and PMS concentration increased, so did the K value. On the other hand, the K value increased firstly and then decreased with the rise of pH value in the catalytic system. And the catalytic degradation rate reached its maximum value (0.1502 min -1 ) at pH = 7 in the catalytic system. Interestingly, the presence of Cl - in the system would be beneficial for promoting the catalytic degradation efficiency. Conversely, the existence of CO 3 2- in the system would obviously inhibit the catalytic degradation efficiency. The result of the cycling experiments also verified that the catalyst possessed excellent stability for the degradation of organic dyes. Furthermore, the researchers conducted quenching experiments and EPR (electron paramagnetic resonance) tests, which revealed the crucial roles of superoxide radicals ( center dot O - 2 ) and singlet oxygen ( 1 O 2 ) in the degradation of organic pollutants. Overall, the excellent catalytic activity of Bi 2 WO 6 in the vis/PMS synergistic catalytic system was attributed to its outstanding visible -light -response photocatalysis activity and the superior ability of bismuth ions in activating PMS.
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页数:12
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