Combined NMR, SAXS, and DLS study of concentrated clear solutions used in silicalite-1 zeolite synthesis

被引:77
作者
Aerts, Alexander
Follens, Lana R. A.
Haouas, Mohamed
Caremans, Tom P.
Delsuc, Marc-Andre
Loppinet, Benoit
Vermant, Jan
Goderis, Bart
Taulelle, Francis
Martens, Johan A.
Kirschhock, Christine E. A.
机构
[1] Katholieke Univ Leuven, Ctr Surface Chem & Catalysis, B-3001 Heverlee, Belgium
[2] Univ Versailles, Inst Lavoisier, F-78035 Versailles, France
[3] FORTH, IESL, GR-71110 Iraklion, Greece
[4] Ctr Biochim Struct, F-34090 Montpellier, France
[5] Katholieke Univ Leuven, Dept Chem Engn, B-3001 Heverlee, Belgium
[6] Katholieke Univ Leuven, Dept Chem, B-3001 Heverlee, Belgium
关键词
D O I
10.1021/cm070693j
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
Concentrated clear solutions, as used for the preparation of Silicalite-1 zeolite, were synthesized from tetrapropylammonium hydroxide, tetraethylorthosilicate, and water. The solutions were analyzed using three techniques: quantitative Si-29 NMR, synchrotron small-angle X-ray scattering (SAXS), and dynamic light scattering (DLS). Si-29 NMR showed the coexistence of silicate oligomers and particles. For the first time, both fractions were analyzed simultaneously, providing a global, quantitative description of the clear solution microstructure. The SAXS patterns, typical of interacting particles, could be used together with the Si-29 NMR deduced particle volume fraction to estimate a particle size. A careful analysis of DLS data of the dynamics of the suspensions revealed the occurrence of two diffusive processes. The faster process is a collective particle diffusion. The slower process corresponds to the particle self-diffusion and is present because of the presence of polydispersity in size, shape, and/or surface charge. The self-diffusion coefficient provides a means to estimate the equivalent hydrodynamic radius. The observations hence reveal a complex, polydisperse mixture of particles present at the onset of the Silicalite-1 zeolite formation. Implications on the proposed zeolite formation mechanisms are briefly discussed.
引用
收藏
页码:3448 / 3454
页数:7
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