A kind of copper zirconium tartrate compound and its preparation method and application
A technology of zirconium compound and copper tartrate, applied in the field of catalysts for solid propellants, can solve the problems of high frequency oscillation instability, low propellant energy, low characteristic signals, etc., and achieve the effect of reducing pressure index and inhibiting unstable combustion
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Embodiment 1
[0025] Preparation of copper-zirconium tartrate double metal compound:
[0026] (1) Weigh 3.0g (0.02mol) of tartaric acid, disperse it in 50mL of deionized water, and fully dissolve it with 3.36g (0.04mol) of sodium bicarbonate to form a clear solution; weigh 4.85g (0.02mol) of copper nitrate trihydrate and remove Ion water was dissolved to form a solution, added to sodium tartrate, stirred and mixed evenly, heated to 50°C, and reacted for 2 hours;
[0027] (2) Weigh 1.6g (0.04mol) of sodium hydroxide and dissolve it in 15mL of deionized water, add it to the solution of step (1), react for 0.5h, weigh 4.3g (0.01mol) of zirconium nitrate and dissolve it in 20mL of deionized water to configure Solution, add copper sodium tartrate solution, heat up to 70°C, react for 3 hours, then cool and stand still, wash the precipitate with deionized water several times, filter and dry to obtain 4.6g of blue-black copper-zirconium tartrate bimetallic compound, Yield 90.2%.
[0028] Characte...
Embodiment 2
[0036] Preparation of copper-zirconium tartrate double metal compound:
[0037] (1) Weigh 3.0g (0.02mol) of tartaric acid, disperse it in 50mL deionized water, and fully dissolve it with 3.36g (0.04mol) sodium bicarbonate to form a clear solution; weigh 4.9g (0.02mol) Ion water was dissolved to form a solution, added to sodium tartrate, stirred and mixed evenly, heated to 60°C, and reacted for 3 hours;
[0038] (2) Weigh 1.6g (0.04mol) of sodium hydroxide and dissolve it in 15mL of deionized water, add it to the solution of step (1), react for 0.5h, weigh 4.3g (0.01mol) of zirconium nitrate and dissolve it in 20mL of deionized water to configure Solution, add copper sodium tartrate solution, heat up to 80°C, react for 3 hours, then cool and stand still, wash the precipitate with deionized water several times, filter, and dry to obtain 4.0 g of blue-black copper-zirconium tartrate bismetal compound, Yield 78.4%.
Embodiment 3
[0040] Preparation of copper-zirconium tartrate double metal compound:
[0041] (1) Weigh 3.0g (0.02mol) of tartaric acid, disperse it in 50mL deionized water, and fully dissolve it with 3.4g (0.04mol) sodium carbonate to form a clear solution; weigh 3.20g (0.02mol) of anhydrous copper sulfate with 30mL deionized water Dissolve in water to form a solution, add it to sodium tartrate, stir and mix evenly, heat up to 70°C, and react for 4 hours;
[0042] (2) Weigh 2.26g (0.04mol) of potassium hydroxide and dissolve it in 15mL of deionized water, add it to the solution of step (1), react for 1h, weigh 4.3g (0.01mol) of zirconium nitrate and dissolve it in 20mL of deionized water to form a solution , added to copper sodium tartrate solution, heated to 90°C, reacted for 5 hours, then cooled and left to stand, the precipitate was washed with deionized water several times, filtered, and dried to obtain 4.2g of blue-black copper-zirconium tartrate bismetal compound, producing The rate...
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