采用含高化学活性基团的乙烯基三氯硅烷(CH2=CHSiCl3)和双(三甲基硅基)碳化二亚胺[Me3Si-N=C=N-SiMe3(BTSC)]作前驱体,在室温的氩气氛下于甲苯中进行缩合化学反应,形成稳定透明SiCN溶胶体系,溶胶经过陈化,形成三维空间结构的SiCN凝胶,最后在高温条件下裂解形成SiCN陶瓷。结果表明干凝胶在800℃时裂解为致密的无定型SiCN陶瓷,并在1400℃析晶出棒状。α-Si3N4,陶瓷产率为68%(质量分数,下同)。
Vinyltrichlorosilane CH 2=CHSiC13 reacted with bis(trimethylsilyl)carbodiimide Me3Si-N=C=N-SiMe3(BTSC) in toluene in argon atmosphere, to form transparent non-oxide SiCN sols system at room temperature. The SiCN sols were deposited to transit highly cross-linked and stable non-oxide SiCN gel. Then the SiCN xerogel was annealed at high temperature in argon atmosphere. The results showed that the xerogel can be pyrolyzed to an amorphous SiCN-ceramic at 800 ℃, and the clubbed silicon nitride α-Si3N4 can be observed at 1400 ℃, and the ceramic yield is 65 wt%.