期刊文献+

以Si-Al凝胶、高岭土水热晶化合成多级孔道催化材料 被引量:5

Synthesis of Hierarchical Catalytic Materials From Si-Al Gel and Kaolin by Hydrothermal Crystallization
下载PDF
导出
摘要 以硅铝凝胶为模板剂,在高岭土制浆过程中加入,经喷雾、焙烧后,在水热条件下晶化合成含有NaY分子筛和基质的多孔复合材料。采用X射线衍射法、N2静态吸附法对所合成的样品进行分析表征,考察了硅铝凝胶的加入量对NaY分子筛相对结晶度、n(SiO2)/n(Al2O3)以及复合材料孔道分布的影响。结果表明,随着硅铝凝胶加入量的增加,晶化产物在介孔范围内的孔容及比表面积均有较大幅度的提高,介孔分布也更为集中;当加入凝胶质量分数为10%时,介孔的孔容及比表面积达到最大,在20%时有所下降。在凝胶加入量为10%时,可以得到BET比表面积为480m2/g、总孔容为0.41mL/g、介孔孔容为0.22mL/g、介孔比表面积为98.9m2/g、结晶度为51.0%、n(SiO2)/n(Al2O3)为5.09的含有NaY分子筛和基质的多孔复合材料。 Composite materials containing NaY molecular sieve and matrix in the form of microspheres were synthesized by hydrothermal crystallization method with Si-Al gel as a template,which was added to the Kaolin slurry then spray-dried and calcined.The samples were characterized by X-ray diffraction,N2 adsorption-desorption.The effects of Si-Al gel amount added to Kaolin slurry on the crystallinity,the silica to alumina ratio and pore size distribution of synthesized catalytic materials were investigated.The results showed that after adding the gel,the pore volume and surface area in the mesoporous range of crystallized product were more substantial rise in referral,the pore size distribution was more narrowed.With added gel mass fraction of 10%,the mesoporous pore volume and surface area of crystallized product reached their largest value,and then declined at 20%.When added gel mass fraction was 10%,the hierarchical catalytic materials were obtained with BET surface area of 480 m2/g,total pore volume of 0.41 mL/g,mesopore pore volume of 0.22 mL/g,mesopore surface area of 98.9 m2/g,crystallinity of 51.0% and silica to alumina ratio of 5.09.
出处 《石油学报(石油加工)》 EI CAS CSCD 北大核心 2014年第1期32-37,共6页 Acta Petrolei Sinica(Petroleum Processing Section)
基金 国家自然科学基金项目(21371055) 湖南省自然科学基金项目(11JJ2008) 湖南省高校创新平台开放基金项目(12K118)资助
关键词 硅铝凝胶 水热晶化 NAY分子筛 多级孔道材料 Si-Al gel hydrothermal crystallization NaY molecular sieve hierarchical materials
  • 相关文献

参考文献10

  • 1CORMA A,DíAZ-CABAIAS M J,MARTíNEZTRIGUERO J,et al.A large-cavity zeolite with wide pore windows and potential as an oil refining catalyst[J].Nature,2002,418(6897):514-517.
  • 2L)PEZ FONSECA R,DE RIVAS B,GUTIERREZORTIZ J I,et al.Characterization of the textural properties of chemically dealuminated Y zeolites[J].Studies in Surface Science and Catalysis,2002,144:717-722.
  • 3MORIN S,AYRAULT P,GNEP N S,et al.Influence of the framework composition of commerical HFAU zeolites on their activity and selectivity in m-xylene transformation[J].Applied Catalysis A:General,1998,166(2):281-292.
  • 4ELANGOVAN S P,OGURA M,DAVIS M E,et al.SSZ-33:A promising material for use as a hydrocarbon trap[J].The Journal of Physical Chemistry B,2004,108(35):13062-13065.
  • 5GROEN J C,BACH T,ZIESE U,et al.Creation of hollow zeolite architectures by controlled desilication of Al-zoned ZSM-5 crystals[J].Journal of the American Chemical Society,2005,127(31):10792-10793.
  • 6JACOBSEN C J H,MADSEN C,HOUZVICKA J,et al.Mesoporous zeolite single crystals[J].Journal of the American Chemical Society,2000,122 (29):7116-7117.
  • 7TAN Q F,BAO X J,SONG T C,et al.Synthesis,characterization,and catalytic properties of hydrothermally stable macro-meso-micro-porous composite materials synthesized via in situ assembly of preformed zeolite Y nanoclusters on kaolin[J].Journal of Catalysis,2007,251(1):69-79.
  • 8ON D T,KALIAGUINE S.Zeolite-coated mesostructured cellular silica foams[J].Journal of the American Chemical,2003,125(3):618-619.
  • 9PATRYLAK L,LIKHNYOVSKYI R,VYPYRAYLENKO V,et al.Adsorption properties of zeolite-containing microspheres and FCC catalysts based on Ukrainian kaolin[J].Adsorption Science & Technology,2001,19(7):525-540.
  • 10KARGE H G,WEITKAMP J,BRANDANI S.Adsorption and Diffusion[M].Berlin Heidelberg:Springer-Verlag,2008-8-15.

同被引文献52

引证文献5

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