Preparation of core-shell hybrid particles based on biomass resveratrol and phosphazene molecules co-assisted bimetallic ZIF achieves efficient flame-retardant modification and mechanical property enhancement of polyurea
Jing Qiao , Guanyue Zeng , Lingfeng Cui , Hua Wang , Hanhua Tan , Fuping Dong , Yuzhu Xiong
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引用次数: 0
Abstract
The evolution of Spray Polyurea Elastomer (SPUA) technology has revolutionized protective coating materials. While market demands have accelerated polyurea (PUA) development, achieving high-performance fire-resistant formulations remains a critical challenge. In this study, a novel core-shell hybrid flame-retardant particle, FPM@ZIF-67/ZIF-8, was successfully synthesized through the precise assembly of bimetallic ZIF onto functional polyphosphazene microspheres (FPM). By strategically incorporating biomass-derived resveratrol and phosphazene molecules to introduce flame-retardant features, such as phosphorus-nitrogen heterocycles and aromatic rings, and capitalizing on the synergistic interaction between these structures and the smoke-suppressing properties of ZIFs, highly efficient flame-retardant PUA composites were successfully prepared. Specifically, the 5 wt % FPM@ZIF-67/ZIF-8 composite achieves UL-94 V-0 rating with limiting oxygen index (LOI) increasing from 20.3 % to 28.4 %. Relative to pure PUA, reductions of 41.6 %, 40.9 %, and 37.8 % were observed in pHRR, THR, and TSP, respectively. Furthermore, robust interfacial adhesion between FPM@ZIF-67/ZIF-8 particles and the PUA matrix, combined with efficient energy dissipation mechanisms, resulted in enhanced tensile strength (20.8 MPa) and elongation at break (1014.6 %). This study advances the design of bio-derived core-shell flame-retardant hybrids, facilitating the creation of high-performance PUA elastomers with balanced fire resistance and mechanical integrity. These findings hold substantial implications for broadening PUA applications in fire-sensitive domains.
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.