In situ investigation of Si-TPA-MFI crystallization using (ultra-) small- and wide-angle X-ray scattering

被引:86
作者
de Moor, PPEA
Beelen, TPM
Komanschek, BU
Diat, O
van Santen, RA
机构
[1] Eindhoven Univ Technol, Schuit Inst Catalysis, NL-5600 MB Eindhoven, Netherlands
[2] SERC, Daresbury Lab, Warrington WA4 4AD, Cheshire, England
[3] European Synchrotron Radiat Facil, F-38043 Grenoble, France
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 1997年 / 101卷 / 51期
关键词
D O I
10.1021/jp9724784
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 formation of precursors and the growth and aggregation of silicalite-1 crystals using tetrapropylammonium as a template (Si-TPA-MFI) has been studied in situ using X-ray scattering techniques. Simultaneous small-angle and wide-angle X-ray scattering (respectively SAXS and WAXS) experiments using synchrotron light showed that the formation of amorphous colloidal aggregates in water clear synthesis mixtures was dependent on the alkalinity of the solutions. In situ time-resolved ultra-small-angle X-ray scattering (USAXS) showed the form factor oscillations of the growing crystals. Fitting of the USAXS patterns to the scattering pattern of spherical particles having a normal particle size distribution showed a linear growth of the average crystal diameter, which was approximately the same for both alkalinities studied. The final size of the crystals was highest for the synthesis mixture having the highest alkalinity, which can be explained in terms of number of viable nuclei formed. At the end of the linear growth the crystals form aggregates corresponding with a diffusion limited aggregation process (mass fractal dimension of 1.8).
引用
收藏
页码:11077 / 11086
页数:10
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