Ionic Liquids: A Versatile Platform for the Design of a Multifunctional Epoxy Networks 2.0 Generation. (September 2022)
- Record Type:
- Journal Article
- Title:
- Ionic Liquids: A Versatile Platform for the Design of a Multifunctional Epoxy Networks 2.0 Generation. (September 2022)
- Main Title:
- Ionic Liquids: A Versatile Platform for the Design of a Multifunctional Epoxy Networks 2.0 Generation
- Authors:
- Livi, Sébastien
Baudoux, Jérôme
Gérard, Jean-François
Duchet-Rumeau, Jannick - Abstract:
- Abstract: Due to their outstanding properties such as high optical transparency, high electrical resistance, high thermal insulation, good thermo-mechanical properties, and dimensional stability, epoxy networks play a key role in the world of thermosetting polymers. In fact, they are widely used in Industry as adhesives, paints and coatings, electrical and electronics applications as well as composite matrices for automotive and aerospace applications. Epoxy networks are issued from epoxy prepolymers composed of two to four oxirane rings able to undergo a polyaddition polymerizations with hardeners (amines, phenols, isocyanates, or acids) or a chain homopolymerization reactions in the presence of initiators such as tertiary amines, imidazoles, or ammonium salts. However, the innovations in this area have reached certain technological limits. Very recently, ionic liquids have shown their potential to be used as new initiators or functional building blocks of epoxy prepolymers and as a novel generation of epoxidized ionic liquid monomers. Thus, a new and innovative pathway has emerged producing a new generation of epoxy thermosets issue from ionic liquids by the concept of 'function through structural design' leading to unprecedented improvements in their physical properties. In fact, epoxy networks can be tuned with glass transition temperatures included from -40 to 170°C depending of the targeted applications. Thus, the polymer/ionic liquid synergy leads to the design andAbstract: Due to their outstanding properties such as high optical transparency, high electrical resistance, high thermal insulation, good thermo-mechanical properties, and dimensional stability, epoxy networks play a key role in the world of thermosetting polymers. In fact, they are widely used in Industry as adhesives, paints and coatings, electrical and electronics applications as well as composite matrices for automotive and aerospace applications. Epoxy networks are issued from epoxy prepolymers composed of two to four oxirane rings able to undergo a polyaddition polymerizations with hardeners (amines, phenols, isocyanates, or acids) or a chain homopolymerization reactions in the presence of initiators such as tertiary amines, imidazoles, or ammonium salts. However, the innovations in this area have reached certain technological limits. Very recently, ionic liquids have shown their potential to be used as new initiators or functional building blocks of epoxy prepolymers and as a novel generation of epoxidized ionic liquid monomers. Thus, a new and innovative pathway has emerged producing a new generation of epoxy thermosets issue from ionic liquids by the concept of 'function through structural design' leading to unprecedented improvements in their physical properties. In fact, epoxy networks can be tuned with glass transition temperatures included from -40 to 170°C depending of the targeted applications. Thus, the polymer/ionic liquid synergy leads to the design and development of new dedicated (multi)functional thermosetting materials with improved properties such as ionic conductivity, chemical and thermal stability, fire retardancy, water barrier properties and mechanical performances. The aim of this review is to point out the potential of this novel class of ionic thermoset materials in the field of epoxy thermosets. Graphical abstract: Image, graphical abstract … (more)
- Is Part Of:
- Progress in polymer science. Volume 132(2022)
- Journal:
- Progress in polymer science
- Issue:
- Volume 132(2022)
- Issue Display:
- Volume 132, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 132
- Issue:
- 2022
- Issue Sort Value:
- 2022-0132-2022-0000
- Page Start:
- Page End:
- Publication Date:
- 2022-09
- Subjects:
- Ionic liquids -- Epoxy networks -- Epoxidized ionic liquids -- Functional properties
Ethylammonium Nitrate [EtNH3][NO3] -- 1-decyl-3-methylimidazolium chloride [C10mim][Cl] -- 1-decyl-3-methylimidazolium tetrafluoroborate [C10mim][BF4] -- 1-decyl-3-methylimidazolium dicyanamide [C10mim][N(CN)2] -- 1-butyl-3-methylimidazolium tetrafluoroborate [C4mim][BF4] -- 1-butyl-3-methylimidazolium dicyanamide [C4mim][N(CN)2] -- 1-ethyl-3-methylimidazolium dicyanamide [C2mim][N(CN)2] -- 1-ethyl-3-methylimidazolium thiocyanate [C2mim][SN] -- 1-ethyl-3-methylimidazolium phosphate [C2mim][PO4] -- 1-ethyl-3-methylimidazolium acetate [C2mim][OAc] -- 1-methyl-3-methylimidazolium sulfonate [C1mim][RSO3] -- 1-(3-aminopropyl)-3-butylimidazolium bis(trifluoromethanesulfonyl)imide [apbim] [NTf2] -- tetrabutylammonium leucine [N4444][Leu] -- Ethylpyridinium tetrafluoroborate [C2Py] [BF4] -- Ethylpyridinium hexafluorophosphate [C2Py] [PF6] -- 1-octadecyl-3-methylimidazolium tetrafluoroborate [C18mim][BF4] -- 1-ethyl-3-methylimidazolium tetrafluoroborate [C2mim][BF4] -- 1-ethyl-3-methylimidazolium hexafluorophosphate [C2mim][PF6] -- 1-(2-hydroxyethyl-3-methylimidazolium) chloride [EtOHmim][Cl] -- trihexyl(tetradecyl)phosphonium bis (2, 4, 4-trimethylpentyl)phosphinate [P66614][TMP] -- trihexyl(tetradecyl)phosphonium dicyanamide [P66614][N(CN)2] -- trihexyl(tetradecyl)phosphonium bis(trifluoromethanesulfonyl)imide [P66614][NTf2] -- trihexyl(tetradecyl)phosphonium acetate [P66614][EtOAc] -- trihexyl(tetradecyl)phosphonium bis(2-ethylhexyl)phosphate) [P66614][EHP] -- tributyl(ethyl)phosphonium diethylphosphate [P4442][DEP] -- Bisphenol A diglycidyl ether (DGEBA) -- diphenylolpropane diglycidylether (ED-20) -- 4, 4-diaminodiphenylmethane (DDM) -- 4, 4-methylenebis (3-chloro-2, 6-diethylaniline) (MCDEA) -- methyltetrahydrophtalic anhydride (MTHPA) -- isomethyltetrahydrophtalic anhydride (IMTHPA) -- 3, 5-diethyltoluene-2, 6-diamine and 3, 5-diethyltoluene-2, 4-diamine (DETDA) -- diaminodiphenylsulfone (DDS) -- methyldiethanolamine (MDEA) -- Polyoxypropylenediamine (Jeffamine®D230, Jeffamine®D400, Jeffamine®D2000) -- 9, 10-dihydro-9-oxa-10-phosphaphenanthrene (DOPO) -- Poly(ether sulfone) (PES) -- Polyphenylene ether (PPE) -- Poly(ether imide) (PEI) -- Poly(acrylonitrile) (PAN) -- Poly(vinylidene fluoride) (PVDF) -- Polymethylmethacrylate) (PMMA) -- Polypropylene (PP) -- Polyamide (PA) -- Poly(ethylene glycol) (PEG) -- PEG diglycidyl ether (PEGGE) -- Poly(propylene glycol)diglycidyl ether (PPOGE) -- ethylene glycol diglycidyl ether (EGGE) -- diamino-terminated PEG (PEGBA) -- tetraethylenepentamine (TEPA)
Polymers -- Periodicals
Polymerization -- Periodicals
Polymers -- Industrial applications -- Periodicals
Polymères -- Périodiques
Polymérisation -- Périodiques
547.7 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00796700 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.progpolymsci.2022.101581 ↗
- Languages:
- English
- ISSNs:
- 0079-6700
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6873.570000
British Library DSC - BLDSS-3PM
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