Tiantian Zhang , Siqi Huo , Guofeng Ye , Cheng Wang , Qi Zhang , Yijiao Xue , Pingan Song , Hao Wang , Zhitian Liu
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引用次数: 0
Abstract
Based on sustainable development strategy and practical application requirement, it is crucial to develop high-strength, recyclable, and flame-retardant polyurethane (PU) elastomers. Hence, a flame-retardant, reprocessable, high-performance polyurethane elastomer (PU-DP 1–7) with dynamic boronic ester bonds and phosphorus-containing groups was well-designed and prepared. The chemical structure of PU-DP 1–7 was confirmed by Fourier transform infrared spectrometry (FTIR) and X-ray photoelectron spectroscopy (XPS). PU-DP 1–7 shows a transmittance of about 60 % at the wavelength of 900 nm, and phosphorus and boron elements are evenly distributed within its surface, confirming the formation of uniform cross-linking network. The inclusion of phosphorus-and boron-containing groups endows PU-DP 1–7 with a vertical combustion (UL-94) V-0 rating, indicative of desired flame retardancy. In addition, PU-DP 1–7 exhibits a tensile strength of 42.7 MPa and an elongation at break of 616.9 %, with high adhesion strengths towards various substrates due to abundant hydrogen bonds within its network. Furthermore, the dynamic borate ester bonds endow PU-DP 1–7 with superior physical recycling and shape-memory properties. After hot-pressing at 130 °C, the reformed PU-DP 1–7 film shows an 83.6 % recovery efficiency in terms of elongation at break. This work presents an integrated strategy to create flame-retardant, recyclable polyurethane elastomers with great mechanical and shape-memory performances by introducing phosphorus-containing segments and dynamic boronic ester bonds.
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.