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首页> 外文期刊>Microporous and mesoporous materials: The offical journal of the International Zeolite Association >Step-like crystallization of BEA zeolite: Accumulation of oligomeric species in liquid phase followed by the conversion of solid phase to crystals
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Step-like crystallization of BEA zeolite: Accumulation of oligomeric species in liquid phase followed by the conversion of solid phase to crystals

机译:BEA沸石的分步结晶:液相中低聚物质的积累,然后固相转化为晶体

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In this study, the hydrothermal reactions of the synthesis mixtures of BEA zeolite and the synthesis cakes prepared by the filtration of the synthesis mixtures were investigated. The crystallization curves constructed based on the XRD patterns and the SEM images of the solid phases recovered at different reaction times exhibited step-like curves characterized by very long induction periods (70 h for the synthesis mixtures and 37 h for the synthesis cakes) and a short crystal growth time (4 h for both) at 150 degrees C. The higher concentration of the reactants in the synthesis cakes than in the synthesis mixture quickly generated more nuclei, consequently forming smaller crystals. In order to elucidate the changes occurring in the course of the hydrothermal reaction, a total of seven additional analysis techniques including Si-29 MAS NMR spectra, TEM, IR, and UV-Vis spectra were applied to the solid and liquid phases recovered at various times. No significant changes were observed in the solid phases during the induction period in terms of the crystallinity, chemical environment of silicon atoms, porous properties, capture state of structure-directing agent, and the IR bands of the hydroxyl groups, whereas the contents of oligomeric aluminosilicates increased in the liquid phases. Based on these analyses, the long induction periods were required for sufficient accumulation of the building blocks, and the blocks rapidly assembled to form BEA zeolite crystals in the subsequent growth stage, resulting in the step-like crystallization curves. (C) 2016 Elsevier Inc. All rights reserved.
机译:在这项研究中,研究了BEA沸石合成混合物与通过过滤合成混合物而制备的合成饼的水热反应。基于在不同反应时间回收的固相的XRD图谱和SEM图像构建的结晶曲线呈现出阶梯状曲线,其特征在于非常长的诱导时间(合成混合物70 h,合成饼37 h)和在150摄氏度时晶体生长时间较短(两种晶体都为4小时)。合成饼中反应物的浓度高于合成混合物中的反应物的浓度,很快会产生更多的核,从而形成更小的晶体。为了阐明在水热反应过程中发生的变化,将总共七种其他分析技术(包括Si-29 MAS NMR光谱,TEM,IR和UV-Vis光谱)应用于在各种温度下回收的固相和液相次。在诱导期的固相中,在结晶度,硅原子的化学环境,多孔性质,结构导向剂的俘获状态和羟基的IR谱带方面均未观察到显着变化,而低聚物的含量液相中的铝硅酸盐增加。根据这些分析,需要较长的诱导期才能使积木充分积聚,并且在随后的生长阶段将积木迅速组装以形成BEA沸石晶体,从而形成阶梯状的结晶曲线。 (C)2016 Elsevier Inc.保留所有权利。

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