A synthetic method of a superhigh temperature resistant
zirconium carbide ceramic precursor belongs to preparation methods of
ceramic precursors. The synthetic method includes firstly, dissolving 6.44g
zirconium oxychloride in 50 mL absolute
methanol, stirring the mixture at a
room temperature for dissolving, subjecting the mixture to ice bath for cooling, dropwise adding 2.4g-3.47g saligenin, finally dropwise adding 4.24g
triethylamine at a dropping speed of 1 droplet per second, and subjecting the mixture to magnetic stirring in the process of the dropping adding; after the dropping adding, removing the ice bath and stirring the mixture at a
room temperature for 4 hours; then subjecting the mixture to rotary
evaporation for 10 minutes to evaporate solvents, adding 50 mL
tetrahydrofuran, stirring the mixture at a
room temperature for 2 hours, and performing suction
filtration to remove a
precipitation of
triethylamine hydrochloride; subjecting the mixture to rotary
evaporation for 15 minutes to evaporate the solvents of colatuie, adding 100 mL hexyl
hydride, stirring the mixture at a room temperature for 12-48 hours, performing
filtration to obtain a pale yellow
precipitation, and subjecting the pale yellow
precipitation to
vacuum drying for three hours to obtain the
zirconium carbide ceramic precursor. The synthetic method of the superhigh temperature resistant
zirconium carbide ceramic precursor has the advantages that the even dispersing of modular zirconium components in precursor reins is achieved, the solidification group saligenin are contained in the ceramic precursor so that crosslinking solidification is facilitated, the synthesis temperature is low, the
reaction speed is rapid, and the
toxicity of solvents is small.