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Sökning: id:"swepub:oai:DiVA.org:kth-144970" > Bringing D-limonene...

Bringing D-limonene to the scene of bio-based thermoset coatings via free-radical thiol-ene chemistry : macromonomer synthesis, UV-curing and thermo-mechanical characterization

Claudino, Mauro (författare)
KTH,Ytbehandlingsteknik
Mathevet, Jeanne-Marie (författare)
KTH,Fiber- och polymerteknologi
Jonsson, Mats (författare)
KTH,Tillämpad fysikalisk kemi
visa fler...
Johansson, Mats K. G. (författare)
KTH,Ytbehandlingsteknik
visa färre...
 (creator_code:org_t)
2014
2014
Engelska.
Ingår i: Polymer Chemistry. - : Royal Society of Chemistry (RSC). - 1759-9954. ; 5:9, s. 3245-3260
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • The increasing pursuit for bio-based plastic materials led us to investigate the potential use of the monoterpene limonene in thermoset synthesis using the free-radical mediated thiol-ene reaction. The high efficiency of this reaction to prepare multifunctional ene-terminated resins, as intermediary macromolecular precursors, for thermosets synthesis was demonstrated under thermal and photoinitiated conditions. Although an excess of terpene favors formation of well-defined macromonomers in organic solution, the characteristic low-vapor pressure of limonene hinders its simple removal (or recycling) via evaporation after synthesis. Alteration to an initial thiol-ene stoichiometry of 1 : 0.5 enables production of high molecular weight resins in the form of 'hyperbranched oligomeric-like' structures having moderate polydispersity. UV-curing of these polyfunctional resins combined with equal mole compositions of multifunctional alkyl ester 3-mercapto propionates yields highly sticky, amorphous and flexible elastomers with different thermo-mechanical properties. These can be further modulated by varying the amount of unreacted thiol occluded within the networks working as a plasticizer. Introduction of a renewable cycloaliphatic structure into the materials offers a convenient way to enhance the glass-transition temperature and stiffness of traditional thiol-ene networks. The materials synthesized may be considered potentially useful as sealants and adhesives in a wide variety of applications including organic coatings. The versatility of UV-irradiation over thermal initiation makes this method particularly suitable for green industrial synthesis processes via thiol-ene chemistry using limonene and multifunctional thiols. The thiol-ene system evaluated herein serves as a model example for the sustainable incorporation of natural diolefinic monomers into semisynthetic thiol-ene networks exhibiting a range of thermo-mechanical properties.

Ämnesord

NATURVETENSKAP  -- Kemi -- Polymerkemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Polymer Chemistry (hsv//eng)

Nyckelord

Characterization
Curing
Mechanical properties
Monomers
Monoterpenes
Organic coatings
Resins
Sealants

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art (ämneskategori)

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