2010
DOI: 10.1016/j.polymdegradstab.2010.04.015
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Thermal stability of magnesium-rich primers based on glycidyl carbamate resins

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Cited by 7 publications
(4 citation statements)
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“…76 A study of the thermal stability of a magnesium rich primer system using the amine cured silane modified glycidyl carbamate resin as a binder system showed that the coatings had exceptionally high thermal stability and resulted in a significant amount of intact char residue after exposure to high temperatures. 77 In another study, a portion of the isocyanate groups in a glycidyl carbamate resin synthesis was replaced with an amino silane, resulting in a resin having both epoxy functional groups and silane groups. 78 Curing of the coatings was through amine curing agents as well as through the moisture-catalyzed sol-gel reaction.…”
Section: Hybrid Sol-gel Systemsmentioning
confidence: 99%
“…76 A study of the thermal stability of a magnesium rich primer system using the amine cured silane modified glycidyl carbamate resin as a binder system showed that the coatings had exceptionally high thermal stability and resulted in a significant amount of intact char residue after exposure to high temperatures. 77 In another study, a portion of the isocyanate groups in a glycidyl carbamate resin synthesis was replaced with an amino silane, resulting in a resin having both epoxy functional groups and silane groups. 78 Curing of the coatings was through amine curing agents as well as through the moisture-catalyzed sol-gel reaction.…”
Section: Hybrid Sol-gel Systemsmentioning
confidence: 99%
“…While most Mg-rich primers have been formulated with either thermoplastic epoxy resins or thermosetting epoxy-amine systems, Ravindran et al reported employing a silane-modified glycidyl carbamate binder crosslinked with a polyamide or a polyamine as the continuous phase of their Mg-rich primer [53]. Trimethoxy aminosilane was reacted with hexamethylene diisocyanate-based biuret (10%, 15% and 20% silane modification) and the product was reacted with glycidol to synthesize the silane-modified binder.…”
Section: Performance and Mechanism Of Corrosion Protection By Mg-richmentioning
confidence: 99%
“…Apart from that, an essential advantage of GC resins is the presence of self-cross-linking reactions of epoxide groups toward the active hydrogens of the carbamate, and the secondary hydroxyl group derived from the ring-opening reaction of epoxide group. , The ring-opening reaction of an epoxide group would generate a secondary hydroxyl group, which reacts with other epoxide groups to produce a cross-linked network, thereby resulting in a high cross-linking density in the epoxy resin . Although GC resins provide excellent physical and chemical properties of epoxy thermosets, the preparation of GC resins typically requires an isocyanate reagent as a starting material to react with glycidol. In addition, the use of isocyanate compounds is regarded as an environmental concern because most of the commercially available isocyanate reagents are produced from hazardous phosgene reagents.…”
Section: Introductionmentioning
confidence: 99%