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微波辅助一步法合成Pd-MCM-41及其催化性能测试

Microwave-Assisted Synthesis of Pd-MCM-41 in One Step and Its Catalytic Properties
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摘要 以介孔分子筛MCM-41作为催化剂的载体,采用微波辅助方法一步合成2种不同n(Pd)/n(Si)的负载型催化剂Pd-MCM-41,采用XRD、FT-IR及N2吸附-脱附对Pd-MCM-41进行表征,并将其应用于催化低浓度甲酸分解反应,考察在常规加热和微波加热条件下,Pd负载量、反应温度和反应时间对甲酸在Pd-MCM-41上分解反应的影响。结果表明,微波辅助成功地合成了Pd-MCM-41催化剂,其对低浓度甲酸分解反应有一定的催化效果;提高反应温度和延长反应时间,均有利于低浓度甲酸分解;与常规加热条件相比,在微波加热条件下Pd-MCM-41对甲酸分解反应的催化效果更好。 Two Pd catalysts with different molar ratios of Pd and Si(n(Pd)/n(Si)) supported on mesoporous molecular sieve MCM-41 were synthesized in one step method assisted by microwave,and characterized by means of XRD,FT-IR and N2 adsorption-desorption.The two Pd-MCM-41 were applied to decomposition reaction of formic acid at low concentration under conventional heating and microwave heating conditions.The influences of Pd loading,reaction temperature and reaction time on the catalytic efficiency of Pd-MCM-41 for formic acid decomposition reaction were studied.The experiment results demonstrated that the Pd-MCM-41 catalyst was successfully synthesized by microwave-assisted method,which had certain catalytic effect on decomposition reaction of formic acid at low concentration.To raise the reaction temperature and to prolong the reaction time both were benefit to decomposition of formic acid.Compared with the formic acid decomposition reaction under conventional heating condition,Pd-MCM-41 had higher catalytic efficiency for the reaction under microwave heating condition.
出处 《石油学报(石油加工)》 EI CAS CSCD 北大核心 2011年第5期732-736,共5页 Acta Petrolei Sinica(Petroleum Processing Section)
基金 中央高校基本科研业务费资助项目(CDJXS10221136) 重庆大学研究生创新基金项目(201005A1A0010332)资助
关键词 微波 Pd-MCM-41 甲酸 催化 microwave Pd-MCM-41 formic acid catalysis
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参考文献12

  • 1王文峰,章永凡,李俊篯,丁开宁.NiO催化甲酸分解机理的密度泛函研究[J].催化学报,2004,25(2):129-132. 被引量:9
  • 2SHUNICHI F, TAKESHI K, TOMOYOSHI S. Unusually large tunneling effect on highly efficient generation of hydrogen and hydrogen isotopes in pH-seleetive decomposition of formic acid catalyzed by a heterodinuclear iridium-ruthenium complex in water[J].J Am Chem Soc, 2010, 132: 1496-1497.
  • 3GRISELDA C C, ADRIAN L B, MIGUEL A B. Infrared study of the adsorption of formic acid on clean and catalysts Ca-promoted Pd/SiO2[J].Applied Catalysis A, 2003, 255: 181-195.
  • 4HARMSEN J M A, JELEMENSKY L, VAN ANDEL- SCHEFFER P J M, et al. Kinetic modeling for wet air oxidation of formic acid on a carbon supported platinum catalyst[J].Appl Catal A, 1997, 165: 499-509.
  • 5KRESGE C T, LEONOWICZ M E, ROTH W J, et al. Ordered mesoporous molecular sieves synthesized by a liquid-crystal template mechanism [J].Nature, 1992, 359: 710-712.
  • 6MARIN-ASTORGA N, PECCHI G, FIERRO J L G, et al. A comparative study of Pd supported on MCM-41 and SiO2 in the liquid phase hydrogenation of phenyl alkyl acetylenes mixtures [J]. Journal of Molecular Catalysis A, 2005, 231: 67-74.
  • 7JOONGJAI P, ORATHAI T, PIYASAN P, et al. Effects of Pd precursors on the catalytic activity and deactivation of silica-supported Pd catalysts in liquid phase hydrogenation[J].Applied Catalysis A, 2005, 292 : 322-327.
  • 8AGNES M, BULCS U R, ZOLTAN K, et al. In situ generation of Pd nanoparticles in MCM-41 and catalytic applications in liquid-phase alkyne hydrogenations [J]. Journal of Molecular Catalysis A, 2007, 264: 170-178.
  • 9TOMONORI K, IKUO A T, YOSHIHIKO O, et al. Liquid phase catalytic hydrodechlorination of aryl chlorides over Pd-A1-MCM-41 catalyst[J].Applied Catalysis B, 2006, 66: 151-160.
  • 10曹渊,袁庆华,穆小静,徐彦芹,刘柏林.EuPO_4:Zn@MCM-41的制备和发光性质(英文)[J].无机化学学报,2010,26(12):2243-2250. 被引量:1

二级参考文献32

  • 1[1]Kubota J, Bandara A, Wada A, Domen K, Hirose C. Surf Sci, 1996, 368(1-3): 361
  • 2[2]Bandara A, Kubota J, Wada A, Domen K, Hirose C. J Phys Chem B, 1997, 101(3): 361
  • 3[3]Matsumoto T, Bandara A, Kubota J, Hirose C, Domen K. J Phys Chem B, 1998, 102(16): 2979
  • 4[4]Bandara A, Kubota J, Wada A, Domen K, Hirose C. Appl Phys B, 1999, 68(3): 573
  • 5[5]Oki S, Mezaki R. J Phys Chem, 1973, 77(4): 447
  • 6[6]Mezaki R, Oki S. J Catal, 1973, 30(3): 488
  • 7[7]Oki S, Mezaki R. Ind Eng Chem, Res, 1988, 27(1): 15
  • 8[8]Shido T, Iwasawa Y. J Catal, 1991, 129(2): 343
  • 9Kuo T W, Chen T M, Mou. J. Lumin., 2010,130:483-487.
  • 10Tian I,, Yang P, Wu H, et al. J. Lumin., 2010,130:717-721.

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