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dc.contributor.authorMai, Ngoc Lan
dc.contributor.authorDo, Ha T.
dc.contributor.authorHoang, Nguyen-Hieu
dc.contributor.authorNguyen, Anh H.
dc.contributor.authorTran, Khanh-Quang
dc.contributor.authorMeijer, Evert Jan
dc.contributor.authorTrinh, Thuat
dc.identifier.citationJournal of Physical Chemistry B. 2020, 124 10210-10218.en_US
dc.description.abstractThe understanding of the formation of silicate oligomers in the initial stage of zeolite synthesis is important. The use of organic structure-directing agents (OSDAs) is known to be a key factor in the formation of different silicate species and the final zeolite structure. For example, tetraethylammonium ion (TEA+) is a commonly used organic template for zeolite synthesis. In this study, ab initio molecular dynamics (AIMD) simulation is used to provide an understanding of the role of TEA+ in the formation of various silicate oligomers, ranging from dimer to 4-ring. Calculated free-energy profiles of the reaction pathways show that the formation of a 4-ring structure has the highest energy barrier (97 kJ/mol). The formation of smaller oligomers such as dimer, trimer, and 3-ring has lower activation barriers. The TEA+ ion plays an important role in regulating the predominant species in solution via its coordination with silicate structures during the condensation process. The kinetics and thermodynamics of the oligomerization reaction indicate a more favorable formation of the 3-ring over the 4-ring structure. The results from AIMD simulations are in line with the experimental observation that TEA+ favors the 3-ring and double 3-ring in solution. The results of this study imply that the role of OSDAs is not only important for the host–guest interaction but also crucial for controlling the reactivity of different silicate oligomers during the initial stage of zeolite formation.en_US
dc.publisherACS - American Chemical Societyen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.titleElucidating the role of tetraethylammonium in the silicate condensation reaction from Ab initio molecular dynamics simulationsen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.source.journalJournal of Physical Chemistry Ben_US
dc.relation.projectNotur/NorStore: NN9554Ken_US

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