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Formation of Porous Polymer Morphology by Microsyneresis During Divinylbenzene Polymerization

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    SYSNO ASEP0443627
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleFormation of Porous Polymer Morphology by Microsyneresis During Divinylbenzene Polymerization
    Author(s) Hanková, Libuše (UCHP-M) RID
    Holub, Ladislav (UCHP-M) RID
    Jeřábek, Karel (UCHP-M) RID, ORCID, SAI
    Source TitleJournal of Polymer Science. Part B, Polymer Physics . - : Wiley - ISSN 0887-6266
    Roč. 53, č. 11 (2015), s. 774-781
    Number of pages8 s.
    Languageeng - English
    CountryUS - United States
    Keywordscrosslinking ; macroporous polymers ; mesopores
    Subject RIVCI - Industrial Chemistry, Chemical Engineering
    R&D ProjectsLH12194 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    Institutional supportUCHP-M - RVO:67985858
    UT WOS000353339900002
    EID SCOPUS84928153089
    DOI10.1002/polb.23693
    AnnotationThis article describes the investigation of the importance of various reaction conditions on microsyneretic pore formation during polymerization of divinylbenzene (DVB) under so-called “solvothermal” conditions. In order to induce microsyneretic pore formation, the most important parameter is an unusually high dilution of monomers with a “good” porogen solvating the polymer chains. High dilution and solvation of the growing poly(DVB) chains promotes the prolongation of the polymer chains rather than their interconnection by crosslinking. Consequently, when the polymer gel density reaches the point where syneresis starts, the polymer network is geometrically too extensive to be broken up into precipitating entities and, instead, porogen droplets are formed within the continuous polymer gel. The pore geometry created by microsyneresis offers high surface area in wide mesopores and hence, high capacity for supporting functional groups or reactions with much better accessibility than narrow pores between polymer microspheres produced by macrosyneresis in conventional styrenic polymer supports.
    WorkplaceInstitute of Chemical Process Fundamentals
    ContactEva Jirsová, jirsova@icpf.cas.cz, Tel.: 220 390 227
    Year of Publishing2016
Number of the records: 1  

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