Xiaohan Li , Yepeng Wang , Yijia Chen , Jiarui Du , Yawen Chen , Huiyun Yu , Ju Huo , Xiaohua Tan , Yakai Feng
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引用次数: 0
Abstract
Although epoxy resins (EPs) exhibit superior overall performance, their use in advanced applications is restricted due to their inherent flammability. Improving epoxy thermosets' flame resistance without sacrificing their overall qualities is still challenging. In this work, a hyperbranched structural flame retardant (DVSiBD) with four flame retardant elements (P, N, B and Si) was synthesized and incorporated into EP to prepare retardant thermosets. The thermosets achieved a UL-94 V-0 rating and a limiting oxygen index (LOI) of 28.3 % following incorporating 4 wt% DVSiBD. Simultaneously, there was a 49.8 % decrease in the peak heat release rate (pHRR) and a 17.4 % reduction in the total heat release (THR). The improved flame-retardant efficacy of DVSiBD is chiefly attributable to the synergistic effects of the phosphorus and nitrogen chain segments, alongside the silicon and boron derivatives, as confirmed by a comprehensive analysis of the condensed and gas phases. Additionally, DVSiBD catalyzed and participated in the curing of EP, resulting in EP thermosets with higher cross-linking density, while preserving high glass transition temperature (Tg) and thermal decomposition temperature. Attributed to its flexible Si-O bond and rigid DOPO aromatic unit, the flexural and impact strength of EP thermosets containing 4 wt% DVSiBD was improved by 17.5 % and 39.9 % compared with EP thermosets without DVSiBD, respectively. This work offers a viable approach for the development of hyperbranched flame retardants that contain P, N, B, and Si flame retardant elements, as well as for the enhancement of the retardancy of EP thermosets.
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.