2009
DOI: 10.1016/j.polymdegradstab.2009.01.008
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Synthesis, characterization, thermal properties and flame retardancy of a novel nonflammable phosphazene-based epoxy resin

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Cited by 211 publications
(68 citation statements)
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“…However, a few new peaks appear at 1056 cm -1 , which might be ascribed to the generation of P-O-P. Similar to the mechanism which has been reported [20,21]. The obtained structure could act as an acid catalyst, accelerating the cleavage of side groups and the breaking of ether groups in poly(phosphazene-aryl amides).…”
Section: Thermal Degradation Propertiessupporting
confidence: 78%
“…However, a few new peaks appear at 1056 cm -1 , which might be ascribed to the generation of P-O-P. Similar to the mechanism which has been reported [20,21]. The obtained structure could act as an acid catalyst, accelerating the cleavage of side groups and the breaking of ether groups in poly(phosphazene-aryl amides).…”
Section: Thermal Degradation Propertiessupporting
confidence: 78%
“…As revealed in Table 3, the averaged value of EHC (av-EHC) for cured CTP-EP/DDM system decreases from 22.73 MJ kg À1 for cured DGEBA/DDM system to 16.65 MJ kg À1 . The reason is that the CTP-EP thermoset containing phosphazene group released noncombustible gases, such as volatile phosphide, N 2 , NH 3 and CO 2 during the combustion process [24,27,42], which could dilute flammable gases and reduce the oxygen concentration around the material. Although the chemical mechanism of action, such as scavenging free radicals in the flame, can not be characterized precisely in this paper, the nonflammable gases could play a role in the gas phase.…”
Section: Cone Calorimetry Of the Cured Epoxy Resinsmentioning
confidence: 99%
“…So it is desirable to obtain novel cyclotriphosphazene-based epoxy materials with excellent comprehensive performance. However, the phosphazene used as primary component for synthesizing the flame retardant epoxy resins was seldom reported [24,27,29,30] and the flame retardant mechanism needs to be further investigated.…”
Section: Introductionmentioning
confidence: 99%
“…Therefore, considering the environmental hazards associated with use of halogenated flame retardants, recent research has focused on development of halogen free flame retardants. [4][5][6][7][8] In contrast to conventional thermally cured and solvent-borne resins, UV-curable systems are widely used in various industries as well as academia due to their high efficiency, lack of volatile organic compounds (VOCs), lower energy consumption, ability to coat heatsensitive devices and circuits, lower processing cost, high chemical resistance, increased production capacity, and the broad variability of formulations. [9][10][11][12][13] Photopolymerizable resins are increasingly being used in various applications, mainly in the coating industry, graphic arts and microelectronics to replace conventional, thermally cured solvent-based coatings.…”
Section: Introductionmentioning
confidence: 99%