Self-assembly of triazolyl-based cyclomatrix polyphosphazene and melamine cyanurate for flame-retardant, smoke-suppressing, and mechanically robust epoxy resin
Xiao-Jie Li , Cai Liu , Cong-Yun Zhang , Zhu-Bao Shao , Bin Zhao
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引用次数: 0
Abstract
Epoxy resin (EP) is widely utilized in construction, rail transit, and structural engineering as coatings, adhesives, and resin matrices for fiber-reinforced composites, owing to its excellent processability, adhesion, thermal stability, and mechanical strength. However, its inherent high flammability significantly restricts its application in scenarios requiring stringent fire safety standards. Addressing this challenge, we developed a novel triazolyl-based cyclomatrix polyphosphazene (HTDA) that self-assembles with melamine cyanurate (MCA) through hydrogen bonding, forming a hybrid flame retardant (HTDA@MCA) with a distinctive lamellar structure. The impact of HTDA and HTDA@MCA on EP's thermal stability, fire resistance, and mechanical performance was systematically evaluated. Compared to HTDA alone, the HTDA@MCA hybrid demonstrated superior performance, significantly enhancing EP's elastic modulus, crosslink density, and glass transition temperature. At HTDA@MCA loadings of 7.5 % and 10 %, EP achieved a UL-94 V-0 rating and limiting oxygen index (LOI) values of 28.6 % and 29.4 %, respectively. Cone calorimeter and smoke density tests further revealed a 68 % reduction in peak heat release rate and a 54.8 % decrease in smoke production. The excellent dispersion and unique lamellar structure of HTDA@MCA contributed to significant improvements in EP's mechanical properties. This study proposes an innovative strategy for simultaneously improving the fire safety, thermal stability, and mechanical strength of EP, providing valuable guidance for the development of high-performance polymeric materials.
期刊介绍:
Polymer Degradation and Stability deals with the degradation reactions and their control which are a major preoccupation of practitioners of the many and diverse aspects of modern polymer technology.
Deteriorative reactions occur during processing, when polymers are subjected to heat, oxygen and mechanical stress, and during the useful life of the materials when oxygen and sunlight are the most important degradative agencies. In more specialised applications, degradation may be induced by high energy radiation, ozone, atmospheric pollutants, mechanical stress, biological action, hydrolysis and many other influences. The mechanisms of these reactions and stabilisation processes must be understood if the technology and application of polymers are to continue to advance. The reporting of investigations of this kind is therefore a major function of this journal.
However there are also new developments in polymer technology in which degradation processes find positive applications. For example, photodegradable plastics are now available, the recycling of polymeric products will become increasingly important, degradation and combustion studies are involved in the definition of the fire hazards which are associated with polymeric materials and the microelectronics industry is vitally dependent upon polymer degradation in the manufacture of its circuitry. Polymer properties may also be improved by processes like curing and grafting, the chemistry of which can be closely related to that which causes physical deterioration in other circumstances.