期刊文献+

Keggin型缺位杂多阴离子PW_(11)O_(39)^(7-)电催化降解硝基苯 被引量:2

Electrocatalytic Degradation of Nitrobenzene by Keggin-type Lacunary Heteropolyanion PW_(11)O_(39)^(7-)
原文传递
导出
摘要 以Keggin型缺位杂多阴离子PW11O397-(PW11)为电催化剂,硝基苯(NB)为模型污染物,研究了Na2SO4-NaHSO4介质中PW11O397-对NB的电催化降解作用.实验结果表明,在pH=2.5,E=-0.6V和O2流速为60mL·min-1的条件下,初始浓度为0.5mmol·L-1的硝基苯反应80min即完全降解,反应120min总有机碳(TOC)去除达42%.硝基苯的电催化降解服从准一级反应动力学模型,室温下其表观速率常数kobs的大小与NB的初始浓度有关,当NB的初始浓度为0.5,0.9和1.3mmol·L-1时,kobs值分别为1.0×10-1,6.0×10-2和4.1×10-2min-1. With Keggin-type lacunary heteropolytungstate anion PW1 1 O 397― as an electrocatalyst and nitrobenzene (NB) as a model pollutant the electrocatalytic degradation of NB by PW1 1O 397― in Na2SO4+ NaHSO4 medium was studied. Experimental results revealed that a complete NB degradation was obtained in less than 80 min in pH 2.5 Na2SO4-NaHSO4 solution containing 0.5 mmol·L-1 NB at the potential of-0.6 V and the O2 flow rate of 60 mL·min-1. A total organic carbon (TOC) removal reached 42% at 120 min reaction time. The NB degradation reaction followed the pseudo-first order kinetic regime and the observed rate constants kobs related to the initial NB concentration at room temperature was determined to be 1.0×10-1, 6.0×10-2 and 4.1×10-2 min-1 corresponding to 0.5, 0.9 and 1.3 mmol·L-1 initial NB concentrations, respectively.
出处 《化学学报》 SCIE CAS CSCD 北大核心 2010年第19期1961-1964,共4页 Acta Chimica Sinica
基金 国家自然科学基金(No.20963003) 海南省重点科技项目(Nos.080305 090803) 海南省自然科学基金(No.509009) 吉林省科技发展计划(No.20090595)资助项目
关键词 缺位杂多阴离子 电催化 硝基苯降解 矿化率 lacunary heteropolyanion electrocatalysis nitrobenzene degradation mineralization rate
  • 相关文献

参考文献14

  • 1Zonnevijlle, F.; Tourne, C. M.; Tourne, G. F. Inorg. Chem. 1982, 21, 2742.
  • 2Wei, X. Y.; Wei, Dickman, M. H.; Pope, M. T. J. Am. Chem. Soc. 1998, 120, 10254.
  • 3Radkov, E. V.; Beer, R. H. Inorg. Chim. Acta 2000, 297, 191.
  • 4Watras, M. J.; Teplyakov, A. V. J. Phys. Chem. B 2005, 109, 8928.
  • 5Server-Carrio, J.; Bas-Serra, J.; Gonzalez-Nunez, M.; Garcia-Gastaldi, A.; Jameson, G.; Baker, L.; Acerete, R. J. Am. Chem. Soc. 1999, 121,977.
  • 6Lei, P. X.; Chert, C. C.; Yang, J.; Ma, W. H.; Zhao, J. C.; Zang, L. Environ. Sci. Technol. 2005, 39, 8466.
  • 7华英杰,王崇太,李高仁,童叶翔,李玉光.Keggin型缺位磷钨杂多阴离子的电化学性质及电催化还原过氧化氢[J].化学学报,2009,67(8):795-800. 被引量:9
  • 8Wang, C. T.; Hua, Y. J.; Li, G. R.; Tong, Y. X.; Li, Y. G. Electrochim. Acta 2008, 53, 5100.
  • 9Brevard, C.; Schimpf, R.; Tourn6, G.; Toured, C. M. J. Am. Chem. Soc. 1983, 105, 7059.
  • 10Liu, H.; Wang, C.; Li, X. Z.; Xuan, X. L.; Jiang, C. C.; Cui, H. N. Environ. Sci. Technol. 2007, 41, 2937.

二级参考文献44

共引文献18

同被引文献23

  • 1胡晓君,李荣斌,沈荷生,戴永兵,何贤昶.硼磷共掺杂n型金刚石薄膜的Hall效应、红外光谱和EPR研究[J].无机材料学报,2004,19(4):895-901. 被引量:2
  • 2刘健敏,夏义本,王林军,张明龙,苏青峰.工艺条件对热丝CVD金刚石薄膜电学性能的影响[J].无机材料学报,2006,21(4):1018-1024. 被引量:2
  • 3JORGENSEN K A. Transition-metal-catalyzed epoxida- tions [J]. Chem Rev, 1989, 89:431 -458.
  • 4JORGENSEN K A, SCHISTT B. Metallaoxetanes as in- termediate in oxygen-transfer reactions-reality or fiction [J]. Chem Rev, 1990, 90:1483-1506.
  • 5DRAGO R S. Homogeneous metal-catalyzed oxidations by O2[J]. Coord, Chem Rev,1992, 117:185 -213.
  • 6SADAKANE M, STECKHAN E. Electrochemical proper- ties of polyoxometalates as electrocatalysts [ J ]. Chem Rev,1998, 98:219-237.
  • 7BINETA K, ESSADIK A, LOUIS N, et al. Cooperativity of copper and molybdenum centers in polyoxometalate- based electrocatalysts: cyclic vohammetry, EQCM, and AFM characterization [ J ]. Langmuir, 2006, 22 ( 25 ) : 10416 - 10425.
  • 8SADAKANE M, STECKHAN E. Investigation of the manganese-substituted α - Keggin-heteropolyanion K6SiW11O39Mn(H2O) by cyclic voltammetry and its ap- plication as oxidation catalyst[ J]. J Mol Catal A: Chem- ical, 1996, 114:221-228.
  • 9ESSAADI K, KEITA B, NADJO L, et al. Oxidation of NADH by oxometalates [ J]. J Electroanal Chem, 1994, 367 : 275 - 278.
  • 10BART J C, ANSON F C. Coordination, electron transfer and catalytic chemistry of a ruthenium-substituted hetero- polytungstate anion as revealed in its electrochemical be- havior [J]. J Electroanal Chem, 1995, 390:11 -19.

引证文献2

二级引证文献6

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部