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Insights into the structural transformations of aluminosilicate inorganic polymers: a comprehensive solid-state NMR study

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    SYSNO ASEP0379050
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleInsights into the structural transformations of aluminosilicate inorganic polymers: a comprehensive solid-state NMR study
    Author(s) Brus, Jiří (UMCH-V) RID, ORCID
    Kobera, Libor (UMCH-V) RID, ORCID
    Urbanová, Martina (UMCH-V) RID, ORCID
    Koloušek, D. (CZ)
    Kotek, Jiří (UMCH-V) RID
    Source TitleJournal of Physical Chemistry C. - : American Chemical Society - ISSN 1932-7447
    Roč. 116, č. 27 (2012), s. 14627-14637
    Number of pages11 s.
    Languageeng - English
    CountryUS - United States
    Keywordsinorganic polymers ; phase transition ; water
    Subject RIVCF - Physical ; Theoretical Chemistry
    R&D ProjectsGAP108/10/1980 GA ČR - Czech Science Foundation (CSF)
    IAA400400904 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    Institutional supportUMCH-V - RVO:61389013
    CEZAV0Z40500505 - UMCH-V (2005-2011)
    UT WOS000306303800050
    DOI10.1021/jp300181q
    AnnotationTo clarify the problem of undesired crystallization of amorphous aluminosilicate inorganic polymers (AIPs), we used 27Al MQ/MAS spectroscopy that revealed a two-component character of the prepared AIPs. The prevailing fraction of [AlO4]− species (amorphous phase) is charge-balanced by Na+counterions and exhibits considerable distribution of 27Al chemical shifts induced by the variation of Al−O−Si valence angles. In contrast, the minor fraction of [AlO4]− tetrahedra, which can be attributed to the partially ordered domains, shows a broad distribution of quadrupolar parameters that result from variability in the chemical nature of counterions. The partially ordered domains of the phase-unstable AIPs contained a considerably larger amount of [AlO4]− species charge-balanced by H+. Therefore, we assume that the destabilization of AIPs is associated with the presence of bridging hydroxyl groups (Si−OH+−Al, Brønsted-acid sites) that induce breaking of Si−O−Al bonds.
    WorkplaceInstitute of Macromolecular Chemistry
    ContactEva Čechová, cechova@imc.cas.cz ; Tel.: 296 809 358
    Year of Publishing2013
Number of the records: 1  

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