Synthesis in fluoride and hydroxide media and structure of the extra-large pore pure silica zeolite CIT-5

被引:41
作者
Barrett, PA
Diaz-Cabanas, MJ
Camblor, MA
Jones, RH
机构
[1] Univ Politecn Valencia, CSIC, Inst Tecnol Quim, E-46071 Valencia, Spain
[2] Univ Keele, Dept Chem, Keele ST5 5BG, Staffs, England
来源
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS | 1998年 / 94卷 / 16期
关键词
D O I
10.1039/a803263g
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The new extra-large pore molecular sieve CIT-5 has been synthesised in both hydroxide and fluoride aqueous media. It has been found, contrary to previous reports, that Li+ is not an essential component of the synthesis gel, although it accelerates the crystallisation. The pure silica polymorph synthesised in the F- medium presents almost no connectivity defects, in contrast to that synthesised in the OH- medium. IR and Si-29 MAS NMR spectra of the new samples synthesised in the F- medium show very good resolution of bands owing to the high local order which arises from the very low concentration of connectivity defects. The structure of this phase has been reinvestigated and solved successfully by direct methods and refined using synchrotron X-ray powder diffraction data. The framework topology previously proposed for this phase is found to be correct, although the structure is more accurately described in Im2a rather than Imma symmetry. Despite the increase in the number of tetrahedra forming the minimum window of the pore, from 12 to 14, the effective pore diameter of CIT-5 appears to be almost identical to that of the unidimensional 12-ring zeolite SSZ-24.
引用
收藏
页码:2475 / 2481
页数:7
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