研究论文

ZrO2对NiO/CeO2/γ-Al2O3复合催化剂结构的影响

  • 杨修春 ,
  • 卢振光 ,
  • 康晓春 ,
  • 韦亚南
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  • 同济大学材料科学与工程学院,上海 200092

收稿日期: 2008-05-06

  修回日期: 2008-07-03

  网络出版日期: 2009-01-20

Effect of ZrO2 on the Structure of NiO/CeO2/γ-Al2O3 Composite Catalysts

  • YANG Xiu-Chun ,
  • LU Zhen-Guang ,
  • KANG Xiao-Chun ,
  • WEI Ya-Nan
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  • School of Materials Science and Engineering, Tongji University, Shanghai 200092, China

Received date: 2008-05-06

  Revised date: 2008-07-03

  Online published: 2009-01-20

摘要

以Ni(NO3)6H2O、Al(NO3)3·9H2O、ZrOCl8H2O和Ce(NO3)6H2O为原料,采用共沉淀法分别制备了NiO/CeO2/γ-Al2O3和NiO/CeO2-ZrO2/Al2O3催化剂.通过X射线衍射(XRD)、透射电子显微镜(TEM)和近边X射线吸收精细结构(XANES)等方法对催化剂的组成结构进行表征.结果表明,煅烧温度高于600℃时,NiO/CeO2/γ-Al2O3催化剂中的NiO与γ-Al2O3载体发生作用,形成NiAl2O4尖晶石;而NiO/CeO2-ZrO2/Al2O3催化剂中,NiO能够稳定存在,没有NiAl2O4尖晶石生成,且Al2O3与CeO2和ZrO2作用形成一种新的Zr0.30Ce0.45Al0.25O1.87固溶体.

本文引用格式

杨修春 , 卢振光 , 康晓春 , 韦亚南 . ZrO2对NiO/CeO2/γ-Al2O3复合催化剂结构的影响[J]. 无机材料学报, 2009 , 24(1) : 187 -191 . DOI: 10.3724/SP.J.1077.2009.00187

Abstract

Using Ni(NO3)2·6H2O, Al(NO3)3·9H2O,ZrOCl2·8H2O and Ce(NO3)3·6H2O as raw materials, NiO/CeO2/Al2O3 and NiO/CeO2-ZrO2/A2O3 composite catalysts were prepared by co-precipitation method. Structures of the composite catalysts were investigated by X-ray diffraction (XRD), high resolution transmission electron microscope (TEM) and X-ray absorption near edge structure (XANES) spectroscope. Results indicate that NiO phase in NiO/CeO2/γ-Al2O3 catalysts disappears above 600℃ because it interact with γ-Al2O3 to form NiAl2O4 spinel. However, no NiAl2O4 spinel is found in NiO/CeO2-ZrO2/Al2O3 catalysts annealed at 700℃ due to the formation of Zr0.30Ce0.45Al0.25O1.87 solid solution.

参考文献

1]El-Rub Z A, Bramer E A, Brem G, et al. Industrial and Engineering Chemistry Research, 2004, 43(22): 6911-6919.
[2]杨修春,韦亚南,李伟捷. 化工进展,2007,26(3): 326-330.
[3]Nordgreen T, Liliedahl T, Sjostrom K. Fuel, 2006, 85(5-6): 689-694. 
[4]Tomishige K, Kimura T, Nishikawa J, et al. Catalysis Communications, 2007, 8(2): 161-166.
[5]张玉红,熊国兴,盛世善,等. 物理化学学报, 1999, 15(8): 735-741.
[6]Han Y S, Li J B, Ning X S, et al. Materials Science and Engineering A, 2004, 369(1-2): 241-244.
[7]Si R, Zhang Y W, Li S J, et al. J. Phys. Chem. B, 2004, 108(33):12481-12488.
[8]彭新林,龙志奇,崔梅生,等. 中国稀土学报,2002,20(20):104-107.
[9]Janvier C, Pijolat M, Valdivieso F, et al. Solid State Ionics, 2000, 127(3-4): 207-222.
[10]Yang X C, Riehemann W, Dubiel M, et al. Materials Science and Engineering B, 2002, 95(3):299-307.
[11]Yang X C, Rieheman W. Scripta Mater., 2001, 45(4): 435-440.
[12]杨修春,Dubiel M,Hofmeister H,等(YANG Xiu-Chun, et al). 无机材料学报(Journal of Inorganic Materials), 2006, 21(3):677-682.
[13]Mizuno M, Berjoan R, Coutures J P, et al. J. Ceram. Assoc. Jpn., 1975, 83(2):90-96.
[14]Huang S, Li L, Vleugels J, et al. J. Mater. Sci. Technol., 2004, 20(1):75-78.
[15]Greegor R B, Lytle F W, Chin R L, et al. Journal of Physical Chemistry, 1981, 85(11): 1232-1237.
[16]杨修春,刘维学,Dubiel M,等. 功能材料,2005,8(36): 1146-1150.
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