Arvindh Sekar, Nicolas Chauvet, Sandro Lehner, Milijana Jovic, Sithiprumnea Dul, Patrick Rupper, Sabyasachi Gaan
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引用次数: 0
Abstract
Achieving lower heat release rates (HRR) during combustion is one of the key steps toward obtaining flame retardant materials. UPR thermosets, while mechanically strong and chemically durable, show high HRR upon ignition. While most commercial applications focus on blending of metal oxide or other heterogeneous fillers to reduce HRR, they have significant drawbacks like phase segregation, drop in transparency and other features which disfavor their use in UPRs. Herein, a novel, green technique to generate nSiO2 in-situ in UPRs is demonstrated. The method is designed such that the precursors act as nucleating agents covalently bonded to the UPRs and as growth fuel for the nSiO2 production. Apart from major advantages like a uniform phase distribution in the thermoset and transparency, this technique also prevents direct handling of powdered micro or nanoparticles, leading to a safer working environment for the handling of UPRs. The physical, thermal, and mechanical properties analyzed show great promise towards flame retardant composites, as the formed nanocomposite material, with 10 wt% loading of nSiO2 demonstrates a 41 % reduction in total heat release (THR) and a 52 % reduction in total smoke release (TSR), while retaining optical transmission >90 %. On combination with commercial phosphorus containing flame retardant, ammonium polyphosphate (APP), the composite shows an even greater reduction in THR and TSR, while also being self-extinguishing. These compelling features, coupled with the safe nature of generating nanoparticles in-situ, offer substantial benefits of using this nSiO2 approach towards HRR reduction in UPR-based thermosets and advocate for their use in commercial formulations.
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.