Modelling of synchrotron SAXS patterns of silicalite-1 zeolite during crystallization

被引:25
作者
Aerts, Alexander [1 ]
Follens, Lana R. A. [1 ]
Biermans, Ellen [2 ]
Bals, Sara [2 ]
Van Tendeloo, Gustaaf [2 ]
Loppinet, Benoit [3 ]
Kirschhock, Christine E. A. [1 ]
Martens, Johan A. [1 ]
机构
[1] Katholieke Univ Leuven, Ctr Surface Chem & Catalysis, Dept M2S, B-3001 Heverlee, Belgium
[2] Univ Antwerp, EMAT, B-2020 Antwerp, Belgium
[3] FORTH, Inst Elect Struct & Laser, Iraklion 71110, Crete, Greece
关键词
SMALL-ANGLE SCATTERING; CLEAR SOLUTIONS; LIGHT-SCATTERING; GROWTH-KINETICS; SI-29; NMR; NANOPARTICLES; DLS; TPA-SILICALITE-1; PARTICLES; EVOLUTION;
D O I
10.1039/c0cp01592j
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
Synchrotron small angle X-ray scattering (SAXS) was used to characterize silicalite-1 zeolite crystallization from TEOS/TPAOH/water clear sol. SAXS patterns were recorded over a broad range of length scales, enabling the simultaneous monitoring of nanoparticles and crystals occurring at various stages of the synthesis. A simple two-population model accurately described the patterns. Nanoparticles were modeled by polydisperse core-shell spheres and crystals by monodisperse oblate ellipsoids. These models were consistent with TEM images. The SAXS results, in conjunction with in situ light scattering, showed that nucleation of crystals occurred in a short period of time. Crystals were uniform in size and shape and became increasingly anisotropic during growth. In the presence of nanoparticles, crystal growth was fast. During crystal growth, the number of nanoparticles decreased gradually but their size was constant. These observations suggested that the nanoparticles were growth units in an aggregative crystal growth mechanism. Crystals grown in the presence of nanoparticles developed a faceted habit and intergrowths. In the final stages of growth, nanoparticles were depleted. Concurrently, the crystal growth rate decreased significantly.
引用
收藏
页码:4318 / 4325
页数:8
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