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VOC-free tricomponent reaction platform for epoxy network formation mediated by a recyclable ionic liquid

  1. 1.
    SYSNO ASEP0561765
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleVOC-free tricomponent reaction platform for epoxy network formation mediated by a recyclable ionic liquid
    Author(s) Rebei, Marwa (UMCH-V)
    Mahun, Andrii (UMCH-V) ORCID
    Walterová, Zuzana (UMCH-V)
    Trhlíková, Olga (UMCH-V) RID, ORCID
    Donato, Ricardo Keitel (UMCH-V) ORCID
    Beneš, Hynek (UMCH-V) RID, ORCID
    Source TitlePolymer Chemistry . - : Royal Society of Chemistry - ISSN 1759-9954
    Roč. 13, č. 37 (2022), s. 5380-5388
    Number of pages9 s.
    Languageeng - English
    CountryGB - United Kingdom
    Keywordsepoxy ring-opening ; ionic liquid ; epoxy
    Subject RIVCD - Macromolecular Chemistry
    OECD categoryPolymer science
    R&D ProjectsGA22-05244S GA ČR - Czech Science Foundation (CSF)
    Method of publishingLimited access
    Institutional supportUMCH-V - RVO:61389013
    UT WOS000849825800001
    EID SCOPUS85139219614
    DOI10.1039/D2PY01031C
    AnnotationHerein we propose a simple, volatile organic solvent (VOC)-free tricomponent reaction platform for the stoichiometric step-growth polymerization between diepoxy resins and dicarboxylic acid in an imidazolium IL medium. The established epoxy resin diglycidyl ether of bisphenol A (DGEBA), as well as the bio-based diglycidyl ether of methyl hydroquinone (DGEMHQ), were used as epoxy sources, while bio-sourced succinic acid was used as the binding building block in this reaction platform performed under mild conditions (T = 80–120 °C). Moreover, no co-solvents, co-catalysts or conventional polymerization initiators were used in our platform as the IL acted as both solvent and initiator/catalyst, and as no direct residue was produced, this concept fully complies with most of the 12 principles of green chemistry. In addition, post-reaction IL-recyclability was studied to further prove the sustainability and cost-effectivity of this platform. The ring-opening of DGEBA and DGEMHQ was followed by FTIR analysis and confirmed with NMR, showing a full consumption of the oxirane ring within 3 to 5 h of reaction. Also, MALDI-TOF mass spectrometry was used for the detection of the intermediates formed in different reaction steps to define the initiation mechanism. Finally, crosslinking and network structure of the optimized solid epoxy materials were characterized using dynamic-mechanical and thermogravimetric analysis.
    WorkplaceInstitute of Macromolecular Chemistry
    ContactEva Čechová, cechova@imc.cas.cz ; Tel.: 296 809 358
    Year of Publishing2023
    Electronic addresshttps://pubs.rsc.org/en/content/articlelanding/2022/PY/D2PY01031C
Number of the records: 1  

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