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Effects of Silicon Dioxide/Graphene Oxide Hybrid Modification on Curing Kinetics of Epoxy Resin

[Image: see text] In this study, SiO(2)-grafted graphene oxide (GO-SiO(2)) was prepared using the oxygen-containing group on the GO surface as the active site of the reaction. The chemical structure, morphology, and particle size of GO and GO-SiO(2) were carefully investigated by Fourier transform i...

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Detalles Bibliográficos
Autores principales: Gou, Bingwang, Song, Xiuduo, Wu, Zongkai, Chen, Xuebing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9583634/
https://www.ncbi.nlm.nih.gov/pubmed/36278034
http://dx.doi.org/10.1021/acsomega.2c04505
Descripción
Sumario:[Image: see text] In this study, SiO(2)-grafted graphene oxide (GO-SiO(2)) was prepared using the oxygen-containing group on the GO surface as the active site of the reaction. The chemical structure, morphology, and particle size of GO and GO-SiO(2) were carefully investigated by Fourier transform infrared (FT-IR) spectroscopy, X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), Raman spectroscopy, thermogravimetry, transmission electron microscopy, scanning electron microscopy, and atomic force microscopy, and the results proved that the grafting modification was successful. Furthermore, epoxy (EP)/GO composites were prepared, and the effects of unmodified GO and GO-SiO(2) on the curing kinetics of EP were comparatively studied by differential scanning calorimetry (DSC). The results showed that, compared with neat EP and EP/GO, GO-SiO(2) significantly reduces the curing temperature of the composites, indicating that GO-SiO(2) has a more significant catalytic effect on the curing process of EP. The calculation results of the Kissinger method showed that the curing activation energy of EP/GO-SiO(2) is obviously lower than that of EP/GO and neat EP. Results of the Ozawa method showed that the introduction of GO-SiO(2) reduces the curing activation energy during the whole curing process, and in the middle and late stages of curing (α = 0.5–1) can significantly reduce the curing activation energy. The related mechanism has been proposed.