RESUMO
Magnesium hydroxide, as a green inorganic flame-retardancy additive, has been widely used in polymer flame retardancy. However, magnesium hydroxide is difficult to disperse with epoxy resin (EP), and its flame-retardancy performance is poor, so it is difficult to use in flame-retardant epoxy resin. In this study, an efficient magnesium hydroxide-based flame retardant (MH@PPAC) was prepared by surface modification of 2-(diphenyl phosphine) benzoic acid (PPAC) using a simple method. The effect of MH@PPAC on the flame-retardancy properties for epoxy resins was investigated, and the flame-retardancy mechanism was studied. The results show that 5 wt% MH@PPAC can increase the limiting oxygen index for EP from 24.1% to 38.9%, achieving a V-0 rating. At the same time, compared to EP, the peak heat release rate, peak smoke production rate, total smoke production rate, and peak CO generation rate for EP/5 wt% MH@PPAC composite material decreased by 53%, 45%, 51.85%, and 53.13% respectively. The cooperative effect for PPAC and MH promotes the formation of a continuous and dense char layer during the combustion process for the EP-blend material, significantly reducing the exchange for heat and combustible gases, and effectively hindering the combustion process. Additionally, the surface modification of PPAC enhances the dispersion of MH in the EP matrix, endowing EP with superior mechanical properties that meet practical application requirements, thereby expanding the application scope for flame-retardant EP-blend materials.
RESUMO
In response to serious ecological and environmental problems worldwide, a novel graphene oxide (GO) induction method for the in situ synthesis of GO/metal organic framework (MOF) composites (Ni-BTC@GO) for supercapacitors with excellent performance is presented in this study. For the synthesis of the composites, 1,3,5-benzenetricarboxylic acid (BTC) is used as an organic ligand due to its economic advantages. The optimum amount of GO is determined by a comprehensive analysis of morphological characteristics and electrochemical tests. 3D Ni-BTC@GO composites show a similar spatial structure to that of Ni-BTC, revealing that Ni-BTC could provide an effective framework and avoid GO aggregation. The Ni-BTC@GO composites have a more stable electrolyte-electrode interface and an improved electron transfer route than pristine GO and Ni-BTC. The synergistic effects of GO dispersion and Ni-BTC framework on electrochemical behavior are determined, where Ni-BTC@GO 2 achieves the best performance in energy storage performance. Based on the results, the maximum specific capacitance is 1199 F/g at 1 A/g. Ni-BTC@GO 2 has an excellent cycling stability of 84.47% after 5000 cycles at 10 A/g. Moreover, the assembled asymmetric capacitor exhibits an energy density of 40.89 Wh/kg at 800 W/kg, and it still remains at 24.44 Wh/kg at 7998 W/kg. This material is expected to contribute to the design of excellent GO-based supercapacitor electrodes.