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Electrochemical degradation of reactive brilliant red X-3B with the(CeO2/C)-β-PbO2-PTFE composite electrode
The(CeO2/C)-β-PbO2-PTFE composite electrodes modified by graphite powder,cerium oxide powder,polytetrafluoroethylene(PTFE)and the homemade β-PbO2 powder were prepared by the high pressure molding technique.The X-ray diffraction(XRD)was used to test the purity of the homemade β-PbO2 powder.The surfac...
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Published in: | 中国稀土学报:英文版 2016, Vol.34 (5), p.507-520 |
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Main Author: | |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | The(CeO2/C)-β-PbO2-PTFE composite electrodes modified by graphite powder,cerium oxide powder,polytetrafluoroethylene(PTFE)and the homemade β-PbO2 powder were prepared by the high pressure molding technique.The X-ray diffraction(XRD)was used to test the purity of the homemade β-PbO2 powder.The surface structure and electrical property of electrodes were characterized by using scanning electron microscopy(SEM)and the cyclic voltammetry curves(CV).Those images indicated that in electrolysis the(CeO2/C)-β-PbO2-PTFE composite electrodes had higher activity than the β-PbO2-PTFE electrodes,as good as the excellent catalytic performance.In the electrode system the composite electrodes were applied to treat reactive brilliant red(RBR)X-3B solution and we studied the degradation influence factors and the reaction mechanism.The results showed that the electrode system was well in treating RBR X-3B solution with the 20%(CeO2/C)-β-PbO2-PTFE composite electrodes at the initial 100 mg/L RBR X-3B concentration,Na2SO4 concentration of 0.35 mol/L,the constant current density of 30 mA/cm~!2 and electrolyte pH =2.After electrolytic time of 90 min,the maximum decolorization and chemical oxygen demand(COD)removal rates reached 88.92% and 54.54%.And the decolorization rate of RBR X-3B was in conformity with pseudo-first-order kinetics equation.The RBR X-3B degradation mechanism in the electrochemical oxidation system was used with LC-MS to analyze the possible intermediates and degradation pathway. |
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ISSN: | 1002-0721 2509-4963 |