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Construction of SiO_2@UiO-66 core-shell microarchitectures through covalent linkage as flame retardant and smoke suppressant for epoxy resins

机译:通过共价键构建SiO_2 @ UiO-66核壳微体系结构作为环氧树脂的阻燃剂和抑烟剂

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The SiO2@metal organic framework (Universitetet i Oslo -66, UiO-66) core-shell microspheres were constructed through covalent linkage between amine groups in UiO-66-NH2 and epoxy groups on the surface of silica. The morphology and size of the SiO2@UiO-66 core-shell microspheres could be simply controlled by tuning the ratio between UiO-66-NH2 and epoxy terminated silica (E-SiO2). As observed by TEM, the SiO2@UiO-66 hybrids showed better dispersion state within epoxy matrix compared to either E-SiO2 or UiO-66-NH2. The incorporation of SiO2@UiO-66 hybrids slightly promoted the thermal degradation of the resultant epoxy composites but improved residual yield. The dynamic mechanical analysis results indicated that the SiO2@UiO-66 hybrids slightly increased the glass transition temperature and the modulus. The SiO2@UiO-66 hybrids exhibited higher efficiency in reducing the heat release rate and the smoke production rate compared to either E-SiO2 or UiO-66-NH2. The influence of the component ratio in SiO2@UiO-66 on flame retardancy of the epoxy composites was also studied by cone calorimeter. Specifically, the SiO2@UiO-66 hybrid with medium ratio (SiO2@UiO-66-2) exhibited maximum reduction in peak heat release rate (-31%), total heat release (-23%) and total smoke production (-16%). The char residues were investigated by the Fourier transform infrared spectra, scanning electron microscopy and X-ray photoelectron spectroscopy, which demonstrated that the enhanced flame retardancy of EP/SiO2@UiO-66-2 was attributable to the continual morphology and high thermal resistance originated from the presence of the silicon and zirconium complex. These favorable characteristics including high flame retardant efficiency and good smoke suppression make SiO2@UiO-66 hybrids promising for flame retardant polymers application.
机译:通过UiO-66-NH2中的胺基与二氧化硅表面的环氧基之间的共价键合,构造了SiO2 @金属有机骨架(Universitetet i Oslo -66,UiO-66)核壳微球。 SiO2 @ UiO-66核壳微球的形貌和尺寸可以通过调节UiO-66-NH2与环氧封端的二氧化硅(E-SiO2)的比例来简单控制。 TEM观察到,与E-SiO2或UiO-66-NH2相比,SiO2 @ UiO-66杂化物在环氧基质中表现出更好的分散状态。 SiO2 @ UiO-66杂化物的掺入稍微促进了所得环氧复合材料的热降解,但提高了残留产率。动态力学分析结果表明,SiO2 @ UiO-66杂化物略微提高了玻璃化转变温度和模量。与E-SiO2或UiO-66-NH2相比,SiO2 @ UiO-66杂化体在降低放热率和烟雾产生率方面显示出更高的效率。锥量热仪还研究了SiO2 @ UiO-66中组分比对环氧复合材料阻燃性能的影响。具体而言,中等比例(SiO2 @ UiO-66-2)的SiO2 @ UiO-66杂化体在峰值放热率(-31%),总放热(-23%)和总烟雾产生(-16 %)。通过傅立叶变换红外光谱,扫描电子显微镜和X射线光电子能谱研究了焦炭残留物,表明EP / SiO2 @ UiO-66-2的阻燃性增强是由于其连续的形貌和高耐热性所致。硅锆配合物的存在。这些良好的特性(包括高阻燃效率和良好的抑烟性)使SiO2 @ UiO-66杂化材料有望用于阻燃聚合物。

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