Articles producció científica> Enginyeria Mecànica

Acetoacetate based thermosets prepared by dual-Michael addition reactions

  • Identification data

    Identifier: imarina:5864935
  • Authors:

    Konuray O
    Fernández-Francos X
    Ramis X
    Serra Á
  • Others:

    Author, as appears in the article.: Konuray O; Fernández-Francos X; Ramis X; Serra Á
    Department: Enginyeria Mecànica
    e-ISSN: 2073-4360
    URV's Author/s: Fernández Francos, Xavier / Serra Albet, Maria Angels
    Keywords: Thiol-acrylate Photopolymerization Networks Michael addition Kinetics Free-radical polymerization Epoxy thermosets Dual-curing Divinyl sulfone Click chemistry Acrylate Acetoacetate michael addition divinyl sulfone click chemistry acrylate acetoacetate
    Abstract: © 2019 by the authors. Anovel set of dual-curable multiacetoacetate-multiacrylate-divinyl sulfone ternary materials with versatile and manipulable properties are presented. In contrast to common dual-curing systems, the first stage polymer herein consists of a densely crosslinked, high Tg network as a result of base-catalyzed multiacetoacetate-divinyl sulfone Michael addition. A more flexible secondary network forms after base-catalyzed Michael addition of remaining multiacetoacetate to multiacrylate. Curing is truly sequential as the rates of the two Michael additions are significantly different. Curing kinetics were analyzed using differential scanning calorimetry (DSC) and Fourier-transform infrared (FTIR). The materials at each curing stage were characterized using dynamic mechanical analysis (DMA) and SEM. Although some phase separation was observed in certain formulations, the incompatibilities were minimized when the molar percentage of the acetoacetate-divinyl sulfone polymer network was above 75%. Furthermore, the environmental scanning electron microscopy (ESEM) images of these materials show that the more flexible acetoacetate-acrylate phase is dispersed in the form of polymeric spheres within the rigid acetoacetate-divinyl sulfone matrix. This unique dual microstructure can potentially render these materials highly resilient in applications requiring densely crosslinked polymer architectures with enhanced toughness.
    Thematic Areas: Polymers and plastics Polymer science Odontología General chemistry Farmacia Engenharias ii Ciências biológicas ii Chemistry (miscellaneous) Chemistry (all) Biotecnología Astronomia / física
    licence for use: https://creativecommons.org/licenses/by/3.0/es/
    ISSN: 20734360
    Author's mail: xavier.fernandez@urv.cat angels.serra@urv.cat
    Author identifier: 0000-0002-3492-2922 0000-0003-1387-0358
    Record's date: 2023-02-18
    Journal volume: 11
    Papper version: info:eu-repo/semantics/publishedVersion
    Link to the original source: https://www.mdpi.com/2073-4360/11/9/1408
    Papper original source: Polymers. 11 (9):
    APA: Konuray O; Fernández-Francos X; Ramis X; Serra Á (2019). Acetoacetate based thermosets prepared by dual-Michael addition reactions. Polymers, 11(9), -. DOI: 10.3390/polym11091408
    Licence document URL: https://repositori.urv.cat/ca/proteccio-de-dades/
    Article's DOI: 10.3390/polym11091408
    Entity: Universitat Rovira i Virgili
    Journal publication year: 2019
    Publication Type: Journal Publications
  • Keywords:

    Chemistry (Miscellaneous),Polymer Science,Polymers and Plastics
    Thiol-acrylate
    Photopolymerization
    Networks
    Michael addition
    Kinetics
    Free-radical polymerization
    Epoxy thermosets
    Dual-curing
    Divinyl sulfone
    Click chemistry
    Acrylate
    Acetoacetate
    michael addition
    divinyl sulfone
    click chemistry
    acrylate
    acetoacetate
    Polymers and plastics
    Polymer science
    Odontología
    General chemistry
    Farmacia
    Engenharias ii
    Ciências biológicas ii
    Chemistry (miscellaneous)
    Chemistry (all)
    Biotecnología
    Astronomia / física
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