Articles producció científica> Química Analítica i Química Orgànica

Novel thermal curing of cycloaliphatic resins by thiol-epoxy click process with several multifunctional thiols

  • Datos identificativos

    Identificador: imarina:5130696
    Handle: http://hdl.handle.net/20.500.11797/imarina5130696
  • Autores:

    Guzmán D., Mateu B., Fernández-Francos X., Ramis X., Serra A.
  • Otros:

    Autor según el artículo: Guzmán D., Mateu B., Fernández-Francos X., Ramis X., Serra A.
    Departamento: Química Analítica i Química Orgànica
    Autor/es de la URV: Fernández Francos, Xavier / Serra Albet, Maria Angels
    Palabras clave: Thiol–epoxy Thiol-epoxy Thermosets Squalene Eugenol Epoxy resins Cycloaliphatic epoxides Crosslinking Click chemistry Click
    Resumen: Novel thermosets were prepared by the base-catalysed reaction between a cycloaliphatic resin (ECC) and various thiol crosslinkers. 4-(N,N-Dimethylaminopyridine) (DMAP) was used as base catalyst for the thiol-epox y reaction. A commercial tetrathiol (PETMP) and three different thiols synthesized by us, 6SH-SQ, 3SH-EU and 3SH-ISO, were tested. 6SH-SQ and 3SH-EU were prepared from vinyl or allyl compounds from renewable resources such as squalene and eugenol, respectively. Thiol 3SH-ISO was prepared starting from commercially available triallyl isocyanurate. A kinetic study of the mixtures was performed using differential scanning calorimetr y. Stoichiometric ECC/thiol/DMAP formulations were cured at 120 ∘ Cfor1h,at 150 ∘ C for 1 h and post-cured for 30 min at 200 ∘ C. The materials were characterized using Fourier transform infrared spectroscopy, thermogravimetric analysis and dynamic mechanical thermal analysis. The results revealed that the materials obtained from the synthesized thiols had higher thermal stability and glass transition temperatures than those obtained from the commercial PETMP. In addition, all the materials obtained exhibited very good transparency. This study proves the ability of multifunctional thiols to crosslink cycloaliphatic epoxy resins, leading to more flexible materials than those obtained by cationic homopolymerization of ECC or base- catalysed ECC-anhydride copolymerization.
    Áreas temáticas: Química Polymers and plastics Polymer science Organic chemistry Materials chemistry Materiais Interdisciplinar Farmacia Engenharias iv Engenharias iii Engenharias ii Engenharias i Ciências biológicas ii Ciências biológicas i Ciência de alimentos Biotecnología Biodiversidade Astronomia / física
    ISSN: 09598103
    Direcció de correo del autor: xavier.fernandez@urv.cat angels.serra@urv.cat
    Identificador del autor: 0000-0002-3492-2922 0000-0003-1387-0358
    Página final: 1707
    Fecha de alta del registro: 2023-02-18
    Volumen de revista: 66
    Versión del articulo depositado: info:eu-repo/semantics/acceptedVersion
    Enlace a la fuente original: https://onlinelibrary.wiley.com/doi/abs/10.1002/pi.5336
    URL Documento de licencia: http://repositori.urv.cat/ca/proteccio-de-dades/
    Referencia al articulo segun fuente origial: Polymer International. 66 (12): 1697-1707
    Referencia de l'ítem segons les normes APA: Guzmán D., Mateu B., Fernández-Francos X., Ramis X., Serra A. (2017). Novel thermal curing of cycloaliphatic resins by thiol-epoxy click process with several multifunctional thiols. Polymer International, 66(12), 1697-1707. DOI: 10.1002/pi.5336
    DOI del artículo: 10.1002/pi.5336
    Entidad: Universitat Rovira i Virgili
    Año de publicación de la revista: 2017
    Página inicial: 1697
    Tipo de publicación: Journal Publications
  • Palabras clave:

    Materials Chemistry,Organic Chemistry,Polymer Science,Polymers and Plastics
    Thiol–epoxy
    Thiol-epoxy
    Thermosets
    Squalene
    Eugenol
    Epoxy resins
    Cycloaliphatic epoxides
    Crosslinking
    Click chemistry
    Click
    Química
    Polymers and plastics
    Polymer science
    Organic chemistry
    Materials chemistry
    Materiais
    Interdisciplinar
    Farmacia
    Engenharias iv
    Engenharias iii
    Engenharias ii
    Engenharias i
    Ciências biológicas ii
    Ciências biológicas i
    Ciência de alimentos
    Biotecnología
    Biodiversidade
    Astronomia / física
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