| Literature DB >> 27603448 |
Maria Castro1, Mohamed Haouas2, Ivy Lim1, Hans J Bongard1, Ferdi Schüth1, Francis Taulelle3,4, Gunnel Karlsson5, Viveka Alfredsson6, Eric Breyneart4, Christine E A Kirschhock4, Wolfgang Schmidt7.
Abstract
The formation of silicate nanoaggregates (NAs) at the very early stages of precursor sols and zeolite beta crystallization from silicate nanoparticles (NPs) are investigated in detail using a combination of different analysis methods, including liquid-state 29 Si, 27 Al, 14 N, and 1 H NMR spectroscopy, mass spectrometry (MS), small-angle X-ray scattering (SAXS), X-ray diffraction (XRD), and transmission electron microscopy at cryogenic temperatures (cryo-TEM). Prior to hydrothermal treatment, silicate NAs are observed if the Si/OH ratio in the reaction mixture is greater than 1. Condensation of oligomers within the NAs then generates NPs. Aluminum doped into the synthesis mixtures is located exclusively in the NPs, and is found exclusively in a state that is fourfold connected to silicate, favoring their condensation and aggregation. These results are in agreement with general trends observed for other systems. Silicate NAs are essential intermediates for zeolite formation and are generated by the aggregation of hydrated oligomers, aluminate, and templating cations. Subsequent further intra-nanoaggregate silicate condensation results in the formation of NPs. 1 H and 14 N liquid NMR as well as diffusion ordered spectroscopy (DOSY) experiments provide evidence for weakly restricted rotational and translational mobility of the organic template within NAs as a consequence of specific silicate-template interactions. NAs thus appear as key species in clear sols, and their presence in the precursor sol favors silicate condensation and further crystallization, promoted either by increasing the Si/OH ratio or by heating.Entities:
Keywords: NMR spectroscopy; clear sols; crystal growth; mass spectrometry; nanoparticles; oligomers; small angle scattering; transmission electron microscopy; zeolites
Year: 2016 PMID: 27603448 DOI: 10.1002/chem.201600511
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236