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Novel polyurethane coating technology through glycidyl carbamate chemistry / Peter A. Edwards in JOURNAL OF COATINGS TECHNOLOGY AND RESEARCH, Vol. 2, N° 7 (07/2005)
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Titre : Novel polyurethane coating technology through glycidyl carbamate chemistry Type de document : texte imprimé Auteurs : Peter A. Edwards, Auteur ; Dean C. Webster, Auteur ; Grant Striemer, Auteur Année de publication : 2005 Article en page(s) : p. 517-527 Note générale : Bibliogr. Langues : Américain (ame) Tags : Glycidol polymère Propriété chimique Etude expérimentale thermique Relation mise en oeuvre propriété mécanique Mécanisme réaction Cinétique Résistance choc Dureté solvant Triamine Diamine Durcissement(matière plastique) Epoxyde résine Réactivité Matériau revêtement Carbamate organique Index. décimale : 667.9 Revêtements et enduits Résumé : Glycidyl carbamate chemistry combines the excellent properties of polyurethanes with the crosslinking chemistry of epoxy resins. Glycidyl carbamate functional oligomers were synthesized by the reaction of poly functional isocyanate oligomers and glycidol. The oligomers were formulated into coatings with several amine functional crosslinkers at varying stoichiometric ratios and cured at different temperatures. Properties such as solvent resistance, hardness, and impact resistance were dependent on the composition and cure conditions. Most coatings had an excellent combination of properties. Studies were carried out to determine the kinetics of the curing reaction of the glycidyl carbamate functional oligomers with multifunctional and model amines. Detailed kinetic analysis of the curing reactions was also undertaken. The results indicated that the glycidyl carbamate functional group is more reactive than a glycidyl ether group. DOI : 10.1007/s11998-005-0011-0 En ligne : https://link.springer.com/content/pdf/10.1007%2Fs11998-005-0011-0.pdf Format de la ressource électronique : Permalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=3799
in JOURNAL OF COATINGS TECHNOLOGY AND RESEARCH > Vol. 2, N° 7 (07/2005) . - p. 517-527[article]Réservation
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Code-barres Cote Support Localisation Section Disponibilité 002327 - Périodique Bibliothèque principale Documentaires Disponible Novel water-dispersible glycidyl carbamate (GC) resins and waterborne amine-cured coatings / Umesh D. Harkal in JOURNAL OF COATINGS TECHNOLOGY AND RESEARCH, Vol. 8, N° 6 (11/2011)
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Titre : Novel water-dispersible glycidyl carbamate (GC) resins and waterborne amine-cured coatings Type de document : texte imprimé Auteurs : Umesh D. Harkal, Auteur ; Andrew J. Muehlberg, Auteur ; Peter A. Edwards, Auteur ; Dean C. Webster, Auteur Année de publication : 2011 Article en page(s) : p. 735-747 Note générale : Bibliogr. Langues : Américain (ame) Catégories : Carbamate de glycidyle
Epoxydes
Hydrophilie
Monte-Carlo, Méthode de
Polyuréthanes
Revêtements en phase aqueuse:Peinture en phase aqueuseIndex. décimale : 667.9 Revêtements et enduits Résumé : Water-dispersible glycidyl carbamate (GC) functional resins were synthesized and crosslinked using a water-dispersible amine to form coatings. GC functional resins are synthesized by the reaction of an isocyanate functional compound with glycidol to yield a carbamate (urethane) linkage (–NHCO–) and reactive epoxy group. The combination of both functionalities in a single resin structure imparts excellent mechanical and chemical properties to the coatings. Previous studies on the development of GC coatings have focused on solvent-borne coating systems. In this study, GC resins were modified by incorporating nonionic hydrophilic groups to produce water-dispersible resins. To determine the influence of the content of hydrophilic groups on dispersion stability, aqueous dispersions were made from a series of hydrophilically modified GC resins and characterized for particle size and dispersion stability. The composition of a typical, dispersed GC resin particle was predicted using Monte Carlo simulations. Stable GC dispersions were used to prepare amine-cured coatings. The coatings were characterized for solvent resistance, water resistance, hardness, flexibility, adhesion, and surface morphology. It was observed that GC resins were able to be dispersed in water without using any surfactant and by minimal mixing force (hand mixing) and produced coating films with good properties when crosslinked with a compatible waterborne amine crosslinker. Note de contenu : - EXPERIMENTAL : Materials - Synthesis of mPEG-modified GC resins - Characterization - Coating formulation preparation - Coating performance - Differential scanning colorimetry (DSC) - Thermogravimetric analysis (TGA) - Dynamic mechanical analysis (DMA) - Atomic force microscope (AFM) - Salt spray test
- RESULTS AND DISCUSSION : Synthesis of water-dispersible GC resins - Dispersion stability - Coating formulations - Water and solvent resistance - Water contact angle - Other coating properties - Further analysis of the coating properties - Thermal stability - Salt spray testDOI : 10.1007/s11998-011-9356-8 En ligne : https://link.springer.com/content/pdf/10.1007%2Fs11998-011-9356-8.pdf Format de la ressource électronique : Permalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=12600
in JOURNAL OF COATINGS TECHNOLOGY AND RESEARCH > Vol. 8, N° 6 (11/2011) . - p. 735-747[article]Réservation
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Code-barres Cote Support Localisation Section Disponibilité 13484 - Périodique Bibliothèque principale Documentaires Disponible