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Pd/CeO2催化水中溴酸盐的加氢还原研究 被引量:8

Study on liquid phase catalytic hydrogenation of bromate over Pd/CeO_2 catalyst
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摘要 采用溶胶-凝胶法制备了CeO2载体,以浸渍法和沉积沉淀法制备了负载型催化剂Pd/CeO2.使用透射电镜(TEM)和Zeta电位仪对催化剂进行了表征.结果表明两种材料的等电点都在5.0左右;Pd颗粒在载体表面具有良好的分散性,且Pd负载量越高,Pd颗粒的粒径越大.采用Pd/CeO2催化剂催化溴酸盐加氢还原,发现在溴酸盐初始浓度为0.39mmol/L时,采用沉积沉淀法和浸渍法合成的Pd/CeO2催化剂反应50min后对溴酸盐的去除率分别为100%和71%,表明使用沉积沉淀法合成的催化剂具有较高的催化活性.改变催化剂用量,溴酸盐的催化还原速率不受传质阻力的影响,反应过程符合Langmuir–Hinshelwood模型,即催化还原反应由溴酸盐在催化剂表面的吸附控制.增加Pd的负载量,溴酸盐的还原速率增大.溶液pH值较低时,有利于对溴酸盐的催化还原. CeO2 carrier was synthesized via the sol-gel method,Pd/CeO2 catalysts were prepared using the deposition-precipitation and impregnation method.The catalysts were characterized by TEM and Zeta potential measurement.Results showed the isoelectric points(IEPs) of both catalysts were around 5.0,and metallic Pd particles were well dispersed on CeO2 surface,the average Pd particle sizes on the CeO2 surface grown with the increase of Pd loading amount.Bromate with an initial concentration of 0.39mmol/L was removed by 100% over Pd/CeO2 prepared by the deposition-precipitation method and 71% over Pd/CeO2 prepared by impregnation method after reaction for 50min,exhibiting higher catalytic activity for catalyst prepared by the deposition-precipitation method.The catalytic bromate reduction was not influenced by mass transport limitation.Bromate reduction can be described by the Langmuir–Hinshelwood model,indicating that the reaction was controlled by bromate adsorption.Increasing Pd loading amount resulted in enhanced bromate reduction.Decreasing pH was in favor of catalytic bromate reduction.
出处 《中国环境科学》 EI CAS CSCD 北大核心 2011年第8期1274-1279,共6页 China Environmental Science
基金 国家自然科学基金资助项目(21077050) 江苏省自然科学基金资助项目(BK2010051) 科技部国际科技合作项目(2010DFA91910)
关键词 Pd/CeO2 沉积沉淀法 催化加氢 溴酸盐还原 Pd/CeO2 deposition-precipitation method catalytic hydrogenation bromate reduction
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参考文献18

  • 1Gunten Ursvon, Hoigne Jurg. Bromate formation during ozonation of bromide-containing waters: Interaction of ozone and Hydroxyl Radical reactions [J]. Environmental Science and Technology, 1994,28:1234-1242.
  • 2Ratpukdi Thunyalux, Casey Francis, Thomas Desutter, et al. Bromate formation by ozone-VUV in comparison with ozone and ozone-UV: effects of pH, ozone dose, and VUV power [J]. Journal of environmental engineering, 2011, 5:187-195.
  • 3Chen Huan, Xu Zhaoyi, Wan Haiqin, et al. Aqueous bromate reduction by catalytic hydrogenation over Pd/Al2O3 catalysts [J]. Applied Catalysis B: Environmental, 2010,96:307-313.
  • 4Wang Qiliang, Snyder Shane, Kim Jungwoo, et al. Aqueous ethanol modified nanoscale zerovalent iron in bromate reduction: synthesis, characterization, and reactivity [J]. Environmental Science and Technology, 2009,43:3292-3299.
  • 5Li Xie, Shang Chii. Effects of copper and palladium on the reduction of bromate by Fe(0) [J]. Chemosphere, 2006,64:919- 930.
  • 6Wisniewski Jacek A, Kabsch-korbutowicz Malgorzata. Bromate removal in the ion-exchange process [J]. Desalination, 2010,261: 197-201.
  • 7Kishimoto Naoyuki, Matsuda Nobuaki, et al. Bromate ion removal by electrochemical reduction using an activated carbon felt electrode [J]. Environmental Science and Technology, 2009, 43:2054-2059.
  • 8Huang Winnjung, Cheng Yungling. Effect of characteristics of activated carbon on removal of bromate [J]. Separation and Purification Technology, 2008,59:101-107.
  • 9Paschoal Fabiana Maria Monteiro, Pepping Greg, Zanoni Maria Valniee Boldrin, et al. Photoelectrocatalytic removal of bromate using Ti/TiO2 coated as a photoeathode [J]. Environmental Science and Technology, 2009,43:7496 7502.
  • 10Xu Zhaoyi, Chen Liqiang, Shao Yun, et al. Catalytic Hydrogenation of Aqueous Nitrate over Pd-Cu/ZrO2 Catalysts [J]. Industrial and Engineering Chemistry Research, 2009,48:8356- 8363.

二级参考文献9

  • 1[3]Seker E,Cavataio J,Gulari E,et al. Nitric oxide reduction by propene over silver alumina and silver-gold/alumina catalysts:effect of preparation methods [J]. Appl. Catal.A.,1999,183(1): 121- 134.
  • 2[4]Efthimiadis E A,Lionta G D,Christoforou S C,et al.The effect of CH4,H2O and SO2 on the NO reduction with C3H6 [J]. Catal. Today,1998,40(1):15- 26.
  • 3[5]Burch R,Scire S.Selective catalytic reduction of nitric oxide with ethane and methane on some metal exchanged ZSM-5 zeolities [J]. Appl. Catal. B.,1994,3(4):295- 318.
  • 4[6]Tabata T,Kokitsu M,Okada O. Relationship between methane adsorption and selective catalytic reduction of nitrogen oxide by methane on gallium and indium ion-exchanged ZSM-5 [J]. Appl.Catal. B.,1995,6(3):225- 236.
  • 5[7] Burch R,Halpin E,Sullivan J A. A comparison of the selective catalytic reduction of NOx over Al2O3 and sulphated Al2O3 using CH3OH and C3H8 as reductants [J]. Appl. Catal.B.,1998,17(2): 115- 129.
  • 6[1]Miyadera T.Alumina-supported silver catalysts for the selective reduction of nitric oxide with propene and oxygen-containing organic compounds [J]. Appl. Catal. B.,1993,2(2-3):199- 205.
  • 7[2]Miyadera T. Selective reduction of nitric oxide with ethanol over an alumina-supported silver catalyst [J]. Appl. Catal. B.,1997, 13(2): 157- 165.
  • 8王姝,杨波,余刚.钯/泡沫镍电极对水体中2-氯联苯的电催化脱氯作用[J].中国环境科学,2008,28(6):522-526. 被引量:6
  • 9杨波,余刚.氢解还原法进行环境污染控制[J].化学进展,2009,21(1):217-226. 被引量:9

共引文献17

同被引文献64

  • 1李继,董文艺,贺彬,王刚,杜红,张金松,马军,王宝贞.臭氧投加方式对溴酸盐生成量的影响[J].中国给水排水,2005,21(4):1-4. 被引量:41
  • 2马军,刘晓飞,王刚,李继,张金松,贺彬.臭氧/高锰酸盐控制臭氧氧化副产物[J].中国给水排水,2005,21(6):12-15. 被引量:20
  • 3Abrahamsson K, Xie T M. Direct determination of trace amounts of chlorophenols in fresh water, waste water and sea water [J]. Journal of Chromatography A, 1983,279:199-208.
  • 4U. S. EPA, Appendix A to 40CFR, Part 423-126Priority Pollutants [Z]. 2012.
  • 5WHO. WHO/SDE/WSH/03.04/47. Chlorophenols in drinking water. Background document for preparation of WHO guideline for drinking-water quality [S]. 2003.
  • 6Dang X, Zhang X, Lu Z, et al. Construction of Au@TiO2/graphene nanocomposites with plasmonic effect andsuper adsorption ability for enhanced visible-light-driven photocatalytic organic pollutant degradation [J]. Journal of Nanoparticle Research, 2014,16(2): 1-8.
  • 7Witofiska I A, Walock M J, Binczarski M, et al. Pd-Fe/SiO2and Pd-Fe/Al203catalysts for selective hydrodechlorination of 2,4-dichlorophenol into phenol [J]. Journal of Molecular Catalysis A: Chemical, 2014,393:248-256.
  • 8Zhou J, Wu K, Wang W, et al. Pd supported on boron-doped mesoporous carbon as highly active catalyst for liquid phase catalytic hydrodechlorination of 2,4-dichlorophenol [J]. Applied Catalysis A: General, 2014,470:336-343.
  • 9Chen H, Yan T, Jiang F. Adsorption of Cr (VI) from aqueous solution on mesoporous carbon nitride [J]. Journal of the Taiwan Institute of Chemical Engineers, 2014,105(3/4):255-265.
  • 10Maeda K, Wang X, Nishihara Y, et al. Photocatalytic activities of graphitic carbon nitride powder for water reduction and oxidationunder visible light [J]. The Journal of Physical Chemistry C, 2009,113(12):4940-4947.

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