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Pyrolysis Behavior of Boron-Containing Phenol-Formaldehyde Resin (BPFR) Modified by B_2O_3

机译:通过B_2O_3改性含硼酚醛树脂(BPFR)的热解作业

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In this study, pure boron-containing phenol-formaldehyde resin (BPFR) and boron oxide (B_2O_3) modified BPFR have been pyrolyzed at elevated temperatures in air and their thermal decomposition behavior is mainly explored. The structural evolution and chemical composition change during pyrolysis are characterized by thermal gravity (TG), Fourier-transform infrared (FT-1R) spectroscopy, X-ray diffraction (XRD) and field emission scanning electron microscope (FE-SEM). It is shown that the mass residues of pure BPFR are 27.1 and 8.7 wt.% after being pyrolyzed at 600 and 1000 °C for 2 h, respectively. In comparison with the pure BPFR, the mass residue of _2O_3 modified BPFR is obviously higher, with the values of 72.9 and 39.7 wt.% at 600 °C and 1000 °C, respectively. The results of FT-IR prove the degradation and failure of the resin matrix are mainly resulted from the fracture of methylene and the release of small molecules. The XRD characterization shows the residues are amorphous carbon and B2O3. FE-SEM exhibits the melting _2O_3 layer formed on the surface of the samples which could prevent oxygen from diffusing into composites during oxidation to some extent.
机译:在该研究中,含纯贫酚酚醛树脂(BPFR)和氧化硼(B_2O_3)改性BPFR在空气的升高温度下热解,主要探索其热分解行为。热解期间的结构演化和化学成分变化是通过热重(Tg),傅里叶变换红外(FT-1R)光谱,X射线衍射(XRD)和场发射扫描电子显微镜(Fe-SEM)的表征。结果表明,纯BPFR的质量残留物分别在600和1000℃下热解27.1%和8.7重量%。与纯BPFR相比,_2O_3改性BPFR的质量残余物明显较高,其值分别为600°C和1000°C的72.9和39.7重量%。 FT-IR的结果证明了树脂基质的降解和失效主要是由亚甲基的破裂和释放小分子的裂缝。 XRD表征显示残留物是无定形碳和B2O3。 Fe-SEM表现出在样品表面上形成的熔化_2O_3层,其可以防止氧气在氧化期间在一定程度上漫射到复合材料中。

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