期刊文献+

CuCl_(14)Pc/Y纳米复合材料的制备、表征及其催化性能的研究 被引量:5

Preparation, Characterization and Catalytic Properties of CuCl_(14)PC/Y Nano-Composite
在线阅读 下载PDF
导出
摘要 用沸石合成法制备了CuCl14Pc/Y分子筛纳米复合材料(简称为CuCl14Pc/nano-Y),考察了合成条件对纳米复合材料的粒度影响.用XRD、ICP、TG-DTA、TEM、FTIR、UV-vis及催化反应等对其性能作了表征.结果表明:铜酞菁(CuCl14Pc)经过水热晶化后,部分被分装在纳米Y型分子筛的空腔中,其催化氧化性能较普通CuCl14Pc/Y分子筛复合材料有很大提高. Well-crystallized CuCl14PC/zeolite Y nano-composite of average particle size about 60nm (denoted as CuCl14PC/nano-Y) was successfully synthesized via zeolite synthesis method. The integrity of the nano-zeolite host was confirmed by XRD and TEM. The CuCl14PC complexes entrapped in the nano-hosts were characterized by XRD, TEM, FTIR, TG/DTA, ICP, and UV-vis. CuCl14PC/y samples with different particle sizes in micro-scale were also synthesized by adjusting the temperature and water content. CuCl14PC in nano-Y exhibits the catalytic activity 3.1 times higher than CuCl14PC in normal Y with particle size of 550nm for the liquid phase oxidation of cyclohexane with aqueous H2O2 due to bigger surface areas and shorter diffusion pathways.
出处 《无机材料学报》 SCIE EI CAS CSCD 北大核心 2002年第3期539-544,共6页 Journal of Inorganic Materials
基金 国家自然科学基金(29973028) 国家重点基础研究发展现划项目(G200008009)
关键词 CuCl14Pc/Y 纳米复合材料 制备 表征 催化性能 铜酞菁 分子筛 环己烷 氧化反应 催化剂 CuCl14PC zeolite nanocrystalline cyclohexane oxidation
  • 相关文献

参考文献18

  • 1[1]Ichikawa M,Kimura T,Fukuoka A.Stud.Surf.Sci.Catal.,1994,84:335-342.
  • 2[2]De Vos D E,Jacobs P A.Catal.Today,2000,57:105-114.
  • 3[3]Ernst S,Traa Y,Deeg U.Stud.Surf.Sci.Catal.,1994,84:925-932
  • 4[4]Thibault-Starzyk F,Paoton R F,Jacobs P A.Stud.Surf.Sci.Catal.,1994,84:1419-1424.
  • 5[5]Balkus K J,Khanmamedova A K,Dixon K M,et al.Appl.Catal.,A,1996,143:159-173.
  • 6[6]Balkus K J,Eissa M,Levado R.J.Am.Chem.Soc.,1995,117:10753-10754.
  • 7[7]Raja R,Ratnasamy P.Catal.Lett.,1997,48:1-10.
  • 8[8]Balkus K J,et al.Inorg.Chem.,1994,33:67-72.
  • 9[9]Vinod M P,Das T K,Chandwadkar A J,et al.Materials Chemistry and Physics,1999,58:37-43.
  • 10[10]Armengol E,Corma A,Fornes V,Appl.Catal.A,1999,181:305-312.

同被引文献63

引证文献5

二级引证文献11

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