The paper presents the results of a study of the synthesis of a highly dispersed silicon carbide powder by combining exo- and endothermic reactions (synthesis from elements and carbothermic reduction) using carbon nanofibers as carbon material. The reaction products were studied by the X-ray phase and elemental analyses as well as by scanning electron microscopy using the local energy-dispersive X-ray microanalysis. The specific surface of the samples was determined by the BET method. A sedimentation analysis was performed. The thermo-oxidative stability was studied by synchronous thermogravimetry (TG) and differential scanning calorimetry (DSC). The material obtained under optimal conditions is represented by one phase - high-temperature modification silicon carbide. An average size of aggregated particles is 6.3…7.2 μm. The specific surface area of the samples is up to 8 m2 /g. The content of impurities is insignificant (no more than 4 % by weight). Optimal conditions for the synthesis of silicon carbide with the use of NFC(s) as a reducing agent and carbidizer are the following: the mass ratio of reagents according to SiC carbide stoichiometry, the mass ratio of charges of 1:1, and the process in argon at 1800 °C.
Kvashina T.S, Krutskii Yu.L., Cherkasova N.Yu., Kuzmin R.I., Tyurin A.G. Sintez vysokodispersnogo karbida kremniya iz raznykh shikhtovykh materialov [Synthesis of highly dispersed silicon carbide from various charge materials]. Doklady Akademii nauk vysshei shkoly Rossiiskoi Federatsii – Proceedings of the Russian higher school Academy of sciences, 2017, no. 4 (37), pp. 80–90. doi: 10.17212/1727-2769-2017-4-80-90