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Novel alkyd-type coating resins produced using cationic polymerization / Samim Alam in JOURNAL OF COATINGS TECHNOLOGY AND RESEARCH, Vol. 12, N° 4 (07/2015)
[article]
Titre : Novel alkyd-type coating resins produced using cationic polymerization Type de document : texte imprimé Auteurs : Samim Alam, Auteur ; Deep Kalita, Auteur ; Anurad Jayasooriyamu, Auteur ; Shashi Fernando, Auteur ; Sathyabrata Samanta, Auteur ; James Bahr, Auteur ; Sermadurai Selvakumar, Auteur ; Mukund Sibi, Auteur ; Jessica Vold, Auteur ; Chad Ulven, Auteur ; Bret J. Chisholm, Auteur Année de publication : 2015 Article en page(s) : p. 633-646 Note générale : Bibliogr. Langues : Américain (ame) Catégories : Cyclohexyl vinyle ether
Huile de soja
Oxydation
Polyaddition
Polyvinyl éther
Revêtements:PeintureIndex. décimale : 667.9 Revêtements et enduits Résumé : Novel, partially bio-based poly(vinyl ether) copolymers derived from soybean oil and cyclohexyl vinyl ether (CHVE) were produced by cationic polymerization and investigated for application as alkyd-type surface coatings. Three different polymers were produced and cured clear coatings and free films characterized as a function of CHVE comonomer content and curing conditions. CHVE comonomer content was varied at 0, 25, and 50 wt%, and the three different curing conditions were 1 week at room temperature, 120°C for 1 h, and 150°C for 1 h. The results of the study showed that the thermal, mechanical, and physical properties of the coatings produced from these novel polymers varied considerably as a function of polymer composition and cure temperature. Overall, the results suggest a good potential for these novel copolymers to be used for coatings cured by autoxidation. Compared to conventional alkyd resins, which are produced by high temperature melt condensation polymerization, these poly(vinyl ether)s provide several advantages. These advantages include milder, more energy efficient polymer synthesis, elimination of issues associated with gelation during polymer synthesis, production of polymers with well-defined composition and relatively narrow molecular weight distribution, and elimination of film formation and physical property issues associated with entrained monomers, dimers, trimers, etc. Note de contenu : - EXPERIMENTAL : Materials - Synthesis of homopolymers and copolymers of 2-VOES and CHVE - Preparation of free films and coated panels - Methods - Instrumentation
- RESULTS AND DISCUSSION : Synthesis and characterization of poly(2-VOES-co-CHVE) copolymers - Viscoelastic properties and gel content of cured films - Mechanical properties of cured films - Properties of coated substratesDOI : 10.1007/s11998-015-9667-2 En ligne : https://link.springer.com/content/pdf/10.1007%2Fs11998-015-9667-2.pdf Format de la ressource électronique : Permalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=24396
in JOURNAL OF COATINGS TECHNOLOGY AND RESEARCH > Vol. 12, N° 4 (07/2015) . - p. 633-646[article]Réservation
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Code-barres Cote Support Localisation Section Disponibilité 17366 - Périodique Bibliothèque principale Documentaires Disponible Novel bio-based poly(vinylether)s for coating applications / Bret J. Chisholm in COATINGS WORLD, Vol. 20, N° 9 (09/2015)
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Titre : Novel bio-based poly(vinylether)s for coating applications Type de document : texte imprimé Auteurs : Bret J. Chisholm, Auteur ; Harjoyti Kalita, Auteur ; Deep Kalita, Auteur ; Samim Alam, Auteur ; Andrey Chernykh, Auteur ; Ihor Tarnavchyk, Auteur ; James Bahr, Auteur ; Sathyabrata Samanta, Auteur ; Anurad Jayasooriyamu, Auteur ; Shashi Fernando, Auteur ; Sermadurai Selvakumar, Auteur ; Dona Suranga Wickramaratne, Auteur ; Mukund Sibi, Auteur Année de publication : 2015 Article en page(s) : p. 48-54 Note générale : Bibliogr. Langues : Américain (ame) Catégories : Biomatériaux
Copolymères -- Synthèse
Polyvinyl éther
Revêtements:PeintureIndex. décimale : 667.9 Revêtements et enduits Résumé : Linear, soluble polymers were produced from unsaturated bio-based compounds using a carbocationic polymerization process. The unsaturated bio-based that were first converted to vinyl ether monomers and subsequently polymerized were plant oil triglycerides, cardanol, and eugenol. As a result of the much higher reactivity of the vinyl ether group compared to the unsaturation derived from the bio-based compounds and the ability to tailor the cationic polymerization process, polymerization was exclusively limited to vinyl ether groups. By oreserving the unsaturation derived from the bio-based compounds, the polymers could be crosslinked into insoluble coatings by autoxidation. In addition, the unsaturation can be converted to other functional groups, such as epoxy, which enable other crosslinking mechanisms. This document describes some of the polymers and coatings that have been produced with the technology. Note de contenu : - Polymers based on plant oils
- Polymers based on cardanol
- Polymers based on eugenol
- FIGURES : 1. Schematic illustrating the autoxidation process - 2. Synthetic scheme used to produce a novel soybean oil-based vinyl ether monomer - 3. Polymerization system utilized for the production of plant oil-based polyvinyl ether - 4. Vinyl ether monomers copolymerized with 2-VOES - 5. Variation in Tg with comonomer content for 2-VOES-based copolymer films cured at room temperature by autoxidation - 6. Tack-free time as a function of PEGEVE repeat unit content, and an image of a coated glass panel partially laid over the NDSU logo - 7. Schematic illustrating cardanol ethyl vinyl ether synthesis - 8. Illustration of resonance stabilization of a radical generated by hydrogen abstraction by singlet oxygen - 9. Synthetic scheme used to produce an epoxidised version of poly(EEVE) - 10. Viscoelastic properties of the network derived from epoxidized poly(EEVE) and DETA
- TABLES : 1. Data for cured films of polycardanol ethyl vinyl ether - Data for cured films of polyeugenol ethyl vinyl ether - 3. Data for coatings based on epoxidized polyEEVE and DGEBPA cast and cured on steel substratesPermalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=29442
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Code-barres Cote Support Localisation Section Disponibilité 19365 - Périodique Bibliothèque principale Documentaires Disponible Soy-based UV-curable thiol–ene coatings / Zhigang Chen in JOURNAL OF COATINGS TECHNOLOGY AND RESEARCH, Vol. 7, N° 5 (09/2010)
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Titre : Soy-based UV-curable thiol–ene coatings Type de document : texte imprimé Auteurs : Zhigang Chen, Auteur ; Bret J. Chisholm, Auteur ; Radhika Patani, Auteur ; Jennifer F. Wu, Auteur ; Shashi Fernando, Auteur ; Katie Jogodzinski, Auteur ; Dean C. Webster, Auteur Année de publication : 2010 Article en page(s) : p. 603-613 Note générale : Bibliogr. Langues : Américain (ame) Catégories : Revêtements -- Séchage sous rayonnement ultraviolet Tags : Revêtement 'Séchage sous UV' 'Huile de soja' 'Thiol-ene' Index. décimale : 667.9 Revêtements et enduits Résumé : Novel soy-based thiols and enes were synthesized and characterized. Then, soy-based thiol–ene UV-curable coatings were formulated and their coating physiochemical properties were investigated in detail. The use of biorenewable resources, combined with environmentally friendly UV-curable technology, provides a “green + green” solution to the stricter regulations in the coatings industry. Novel soy-based thiols and enes were synthesized through the Lewis acid-catalyzed ring opening reaction of epoxidized soybean oil with multifunctional thiols or hydroxyl functional allyl compounds. FTIR and NMR confirmed the formation of the target compounds. The soy-based thiols and enes were formulated with petrochemical-based enes and thiols, respectively, to make thiol–ene UV-curable coatings. Typical coating film properties, thermal properties, and photopolymerization kinetics of these coatings were studied. Soy-based thiol–ene coatings having lower functionality thiols and enes have poor UV curability and coating properties, which was attributed to the lower crosslink density. Soy-based thiols and enes with higher functionality can be UV-cured in combination with petrochemical-based enes or thiols even without the presence of free radical photoinitiators. Better coating film properties were obtained from these higher functionality thiol–ene systems that were toughened by commercial hyperbranched acrylates. DOI : 10.1007/s11998-010-9241-x En ligne : https://link.springer.com/content/pdf/10.1007%2Fs11998-010-9241-x.pdf Format de la ressource électronique : Permalink : https://e-campus.itech.fr/pmb/opac_css/index.php?lvl=notice_display&id=9914
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