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dc.contributor.author李鹏zh_CN
dc.contributor.author赵跃民zh_CN
dc.contributor.author王立章zh_CN
dc.contributor.author张延乐zh_CN
dc.contributor.author芦兆青zh_CN
dc.contributor.authorLI Pengzh_CN
dc.contributor.authorZHAO Yue-minzh_CN
dc.contributor.authorWANG Li-zhangzh_CN
dc.contributor.authorZHANG Yan-lezh_CN
dc.contributor.authorLU Zhao-qingzh_CN
dc.date.accessioned2014-10-23T02:51:30Z
dc.date.available2014-10-23T02:51:30Z
dc.date.issued2014-10-28zh_CN
dc.identifier.citation电化学,2014,20(5):493-498.zh_CN
dc.identifier.issn1006-3471zh_CN
dc.identifier.urihttp://dx.doi.org/10.13208/j.electrochem.131021zh_CN
dc.identifier.urihttps://dspace.xmu.edu.cn/handle/2288/80520
dc.description.abstract采用刷涂热解和电镀制得了β-PbO2/Sb-SnO2/Ti电极. 采用X射线衍射(X-ray Diffraction,XRD)和扫描电镜(Scanning Electron Microscope,SEM)进行分析与观察,Sb-SnO2中间层抑制PbF2的生成,NaF促进二氧化铅晶粒的成型与分散,消除了β-PbO2聚团. 据谢乐公式(Scherrer)计算晶粒尺寸为25.2 nm,电极表面结晶度高达100%. 极化测试显示,β-PbO2/Sb-SnO2/Ti电极扩散段电位区、析氧电位和Tafel斜率分别为1.85 ~ 2.15 V、2.08 V和0.84,优于β-PbO2/Ti电极的1.40 ~ 1.80 V、1.75 V和0.36. 使用β-PbO2/Sb-SnO2/Ti、β-PbO2/Ti电极在9 mA·cm-2电流密度对苯酚模拟废水处理240 min,前者COD(Chemical Oxygen Demand)去除率、电流效率(Instant Current Efficiency)高达90.1%和63.28%,优于后者66.9%和44.96%. 寿命测试表明,β-PbO2/Sb-SnO2/Ti电极与β-PbO2/Ti电极相比延长10倍,工业寿命可达8.6a,有较高的工程应用价值.zh_CN
dc.description.abstractThe combination technology of brush pyrolysis and electroplating was employed in the preparation of β-PbO2/Sb-SnO2/Ti electrode. X-ray Diffraction (XRD) and Scanning Electron Microscope (SEM) results showed that the Sb-SnO2 as an interlayer would restrain the formation of lead fluoride and the crystallization degree on the electrode surface could be as high as 100%. The grain size was calculated by Scherrer formula to be 25.2 nm and the agglomeration of lead dioxide was effectively eliminated. The potential span of diffusion control phase, oxygen evolution potential, Tafel slope for the β-PbO2/Sb-SnO2/Ti electrode during the polarization were 1.85 ~ 2.15 V, 2.08 V and 0.84, respectively, which exhibited much better electrochemical properties as compared with those of the β-PbO2/Ti electrode with the values of 1.40 ~ 1.80 V, 1.75 V and 0.36, respectively. Furthermore, the β-PbO2/Sb-SnO2/Ti and β-PbO2/Ti electrodes were taken as anodes participating in the electrocatalysis degradation of phenol simulated wastewater under current density 9 mA·cm-2 within 240 min. Experimental results revealed that the efficiencies of chemical oxygen demand (COD) removal and instant current efficiency (ICE) during phenol degradation were 90.1% and 63.28% for the β-PbO2/Sb-SnO2/Ti electrode, while 66.9% and 44.96% for the β-PbO2/Ti electrode. Ultimately, the accelerated life test was performed to evaluate the service time of β-PbO2/Sb-SnO2/Ti. The results presented that the industrial life of β-PbO2/Sb-SnO2/Ti was 8.6a, which is 10 times longer than that of β-PbO2/Ti,suggesting that β-PbO2/Sb-SnO2/Ti would have a relatively high engineering application value.zh_CN
dc.description.sponsorship国家自然科学基金项目(No. 50908226)、国家自然科学基金创新研究群体项目(No. 51221462)、江苏省自然科学基金基础研究计划资助项目(No. BK201124)和江苏省研究生培养创新工程(No. CXLX13-956)资助zh_CN
dc.language.isozhzh_CN
dc.publisher厦门大学《电化学》编辑部zh_CN
dc.relation.ispartofseries研究论文zh_CN
dc.relation.ispartofseriesArticleszh_CN
dc.source.urihttp://electrochem.xmu.edu.cn/CN/abstract/abstract10110.shtmlzh_CN
dc.subjectSb-SnO2中间层zh_CN
dc.subject&betazh_CN
dc.subject-PbO2/Tizh_CN
dc.subject极化特性zh_CN
dc.subject电流效率zh_CN
dc.subject加速寿命测试zh_CN
dc.subjectstannic and antimony oxides interlayerzh_CN
dc.subject&betazh_CN
dc.subject-PbO2/Tizh_CN
dc.subjectpolarization curvezh_CN
dc.subjectinstant current efficiencyzh_CN
dc.subjectaccelerated life testzh_CN
dc.titleβ-PbO2/Sb-SnO2/Ti电极的苯酚电催化性能研究zh_CN
dc.title.alternativeElectro-Catalytic Properties of β-PbO2/Sb-SnO2/Ti Electrode on Phenol Oxidationzh_CN
dc.typeArticlezh_CN
dc.description.note作者联系地址:1. 中国矿业大学环境与测绘学院环境工程专业,江苏 徐州 221116;2. 中国矿业大学化学化工学院矿物加工专业,江苏 徐州 221116;3. 徐州市工程咨询中心,江苏 徐州 221116zh_CN
dc.description.noteAuthor's Address: 1. School of Environment and Spatial Informatics, China University of Mining and Technology, Xuzhou 22116, Jiangsu, China; 2. School of Chemical Engineering and Technology, China University of Mining and Technology, Xuzhou 22116, Jiangsu, China; 3. Xuzhou engineering consulting center, Xuzhou 22116, Jiangsu, Chinazh_CN
dc.description.note通讯作者E-mail:wlzh0731@126.comzh_CN


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