期刊文献+

MoVBiTeO/SiO_2对丙烷选择氧化制丙烯醛反应的催化性能 被引量:2

Catalytic Performance of MoVBiTeO/SiO_2 for Selective Oxidation of Propane to Acrolein
下载PDF
导出
摘要 用浸渍法制备了一系列不同Mo/V比的MoVBiTeO/SiO2催化剂,并用X射线衍射、拉曼光谱、X射线光电子能谱、程序升温还原和红外光谱等方法对催化剂的结构、氧化还原性质和酸性进行了表征,考察了催化剂对丙烷选择氧化制丙烯醛反应的催化性能.结果表明,Mo与V组分之间存在较强的相互作用,调变了催化剂的结构,并形成了氧化还原循环(V5++Mo5+V4++Mo6+),促进了催化剂中电子和O物种的传递,使催化剂的低温可还原性增强,催化活性提高.Mo组分有利于形成L酸位,而V组分有利于形成B酸位.这可能是丙烯醛选择性随Mo/V比增大而逐渐提高的原因之一.当Mo/V摩尔比为6时,催化剂具有最高的丙烯醛收率(9.7%). A series of MoVBiTeO/SiO2 catalyst samples with different Mo/V ratios were prepared by the impregnation method. The catalyst structure, reducibility, and acidity were characterized by XRD, Raman, XPS, TPR, and FT-IR techniques, and the catalytic performance of the catalyst for selective oxidation of propane to acrolein was evaluated. The results indicated that the interaction between Mo and V components modified the catalyst structure, and the redox cycle of V^5++Mo^5+←→V^4++Mo^6+ was formed. The improvement in the reducibility of the catalyst might be responsible for the increase in propane conversion. The V and Mo components were responsible for B acid and L acid, respectively. When the Mo/V ratio increased, the amount of B acid decreased, and the catalyst selectivity for acrolein increased. Among the investigated catalyst samples, the sample with a Mo/V molar ratio of 6 exhibited the best catalytic performance.
出处 《催化学报》 SCIE CAS CSCD 北大核心 2008年第4期409-414,共6页
基金 国家重点基础研究发展计划(2005CB221408) 国家自然科学基金(20433030,20021002,20423002) 福建省科技重大专项(2005HZ01-3)
关键词 复合氧化物 氧化硅 负载型催化剂 丙烷 选择氧化 丙烯醛 molybdenum vanadium bismuth tellurium composite oxide silica supported catalyst propane selective oxidation acrolein
  • 相关文献

参考文献20

  • 1Bettahar M M, Costentin G, Savary L, Lavalley J C. Appl Catal A, 1996, 145(1/2): 1
  • 2何益明,伊晓东,章小兵,应方,黄传敬,翁维正,万惠霖.MoBiTeO/SiO_2催化剂在丙烷选择氧化反应中的表面结构重组[J].催化学报,2007,28(2):112-116. 被引量:3
  • 3何益明,伊晓东,黄传敬,应方,章小兵,翁维正,万惠霖.丙烷选择氧化制丙烯醛MoBiTeO/SiO_(2)催化剂中Te组分的作用[J].物理化学学报,2007,23(6):851-855. 被引量:2
  • 4Huang Ch J, Jin Y X, Ying F, Wan H L. Chem Lett, 2006, 3S(6): 606
  • 5Grasselli R K. Top Carol, 2001, 15(2-4) : 93
  • 6Luan Z H, Meloni P A, Czernuszewicz R S, Kevan L. J Phys Chem B, 1997, 101(44) : 9046
  • 7Blasco T, Nieto J M L. Appl Catal A, 1997, 157(1/2) : 117
  • 8Williams C C, Ekerdt J G, Jehng J M, Hardcastle F D, TurekA M, Wachs I E. J Phys Chem, 1991, 95(22): 8781
  • 9Asakura K, Nakatani K, Kubota T, Iwasawa Y. J Cotal, 2000, 194(2): 309
  • 10Ayame A, Uchida K, Iwataya M, Miyamoto M. Appl Catal A, 2002, 227(1/2): 7

二级参考文献40

  • 1Bettahar M M, Costentin G, Savary L, Lavalley J C. Appl Catal A, 1996, 145(1-2): 1
  • 2Abon M, Bere K E, Tuel A, Delichere P. J Catal, 1995, 156(1): 28
  • 3Volta J C. Catal Today, 1996, 32(1): 29
  • 4Abdelouahab F B, Oiler R, Guilhaume N, Lefebvre F, Volta J C. J Catal, 1992, 134(1): 151
  • 5Pantazidis A, Burrows A, Kiely C J, Mirodatos C. J Catal, 1998, 177(2): 325
  • 6Spevack P A, McIntyre N S. J Phys Chem, 1993, 97 (42) : 11020
  • 7Champarnaud-Mesiard J C, Blanchandin S, Thomas P,Mirgorodsky A, Merle-Mejean T, Frit B. J Phys Chem Solids, 2000, 61(9): 1499
  • 8Arena F, Parmaliana A. J Phys Chem, 1996, 100(51) : 19994
  • 9Ueda W, Moro-oka Y, Ikawa T. J Catal, 1981,70(2) : 409
  • 10Ueda W, Moro-oka Y, Ikawa T. Chem Lett, 1982, (4) : 483

共引文献3

同被引文献85

引证文献2

二级引证文献3

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