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Perdeuterated ammonium dinitramide and preparation method thereof

A technology of ammonium dinitramide and deuterated nitric acid is applied in the synthesis field of deuterated energetic materials, which can solve the problems of catalyst poisoning and deactivation, cumbersome operation process, increasing preparation difficulty, etc., and achieves reduction of production cost, simple purification, The effect of increasing the scope of application

Active Publication Date: 2020-09-04
BEIJING INSTITUTE OF TECHNOLOGYGY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The intermediate product HN(NO 2 ) 2 It is unstable under acidic conditions and will gradually decompose. It is necessary to continuously take samples to measure the HN(NO 2 ) 2 When the concentration reaches the maximum, the next step of neutralization operation can be carried out, so the operation process is comparatively loaded down with trivial details; in addition, by-products such as ammonium nitrate and ammonium sulfate need to be removed by adsorption separation and solvent elution, which increases the difficulty of preparation (WO97 / 06099[ P].1997-02-20.)
In 2005, VOERDE disclosed an improved production method, which neutralized the intermediate product HN(NO 2 ) 2 N-amidinourea dinitramide salt is generated, which is subsequently reacted with potassium hydroxide to generate KN(NO 2 ) 2 , KN(NO 2 ) 2 Carry out ion exchange with ammonium sulfate again to obtain product dinitramide ammonium; This technological method has significantly reduced the consumption of raw material, has shortened reaction time, but contains a large amount of potassium ions in the dinitramide ammonium produced by this method, will be lost during use Cause catalyst poisoning and deactivation (WO2005 / 070823[P].2005-08-04.)
The above methods are all methods for preparing non-deuterated ammonium dinitramide, and the preparation of non-deuterated ammonium dinitramide cannot be completed by simply replacing the raw materials of the above method

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0018] Place a three-port pressure-resistant device with a volume of 250mL and 39.9g of phosphoric anhydride in a high-precision low-temperature circulating bath at -40°C, and drop 62.7g of phosphoric anhydride at a rate of 5mL / min through a constant pressure dropping funnel. 95% deuterated nitric acid, start stirring at a rate of 150rpm after the dropwise addition, and slowly add 13.3g of deuterated sodium sulfamate to the above solution in batches after the phosphoric anhydride is completely dissolved, and keep the temperature of the mixed solution not higher than -30°C; After the sodium deuterated sulfamate is completely dissolved, seal the reaction device, raise the temperature of the solution to -10°C, keep stirring for 0.5 hours to obtain solution B;

[0019] Place a three-port pressure-resistant device with a volume of 500mL and 12.3g of deuterated N-hydroxyacetamidine in a high-precision medium-temperature circulating bath at 15°C, slowly add 125.8g of deionized water t...

Embodiment 2

[0024] Place a three-port pressure-resistant device with a volume of 500mL and 101.4g of phosphoric anhydride in a high-precision low-temperature circulating bath at -40°C, and drop 147.4g of phosphoric anhydride at a rate of 7mL / min through a constant pressure dropping funnel. 95% deuterated nitric acid, start stirring at a rate of 150rpm after the dropwise addition, and slowly add 26.3g of deuterated lithium sulfamate to the above solution in batches after the phosphoric anhydride is completely dissolved, and keep the temperature of the mixed solution not higher than -30°C; After the lithium deuterated sulfamate is completely dissolved, seal the reaction device, raise the temperature of the solution to -12°C, and keep stirring for 40 minutes to obtain solution B;

[0025]Place a three-port pressure-resistant device with a volume of 1L and 34.0g of deuterated N-hydroxyacetamidine in a high-precision medium-temperature circulating bath at 15°C, slowly add 381.2g of deionized wa...

Embodiment 3

[0030] Place a three-port pressure-resistant device with a volume of 500mL and 139.6g of phosphoric anhydride in a high-precision low-temperature circulating bath at -38°C, and drop 308.4g of phosphoric anhydride at a rate of 10mL / min through a constant pressure dropping funnel. 96% deuterated nitric acid, start stirring at a rate of 200rpm after the dropwise addition, and slowly add 44.8g of deuterated sodium sulfamate to the above solution in batches after the phosphoric anhydride is completely dissolved, keeping the temperature of the mixed solution not higher than -30°C; After the sodium deuterated sulfamate is completely dissolved, seal the reaction device, raise the temperature of the solution to -15°C, and keep stirring for 45 minutes to obtain solution B;

[0031] Place a three-port pressure-resistant device with a volume of 2L and 59.3g of deuterated N-hydroxyacetamidine in a high-precision medium-temperature circulating bath at 10°C, slowly add 734.8g of deionized wat...

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Abstract

The invention discloses perdeuterated ammonium dinitramide and a preparation method thereof, belonging to the technical field of synthesis of deuterated energetic materials. According to the invention, purification is simple, and a high-purity product can be obtained without adsorption and solvent elution; the product does not contain metal ions such as potassium ions, does not cause catalyst poisoning in the use process, and is widened in application range; reaction process is judged by measuring the pH value of a solution, and the reaction endpoint judgment method is simple; and deuterated ammonia gas can be recycled after being collected, so the waste of deuteration raw materials is reduced, and production cost is reduced. Compared with common ammonium dinitramide, the initial decomposition temperature of the perdeuterated ammonium dinitramide is increased to about 150 DEG C, and the thermal stability of the perdeuterated ammonium dinitramide is obviously improved; and crystalline density is increased, and meanwhile, energy characteristic is obviously improved. According to the preparation method disclosed by the invention, the preparation of the perdeuterated ammonium dinitramide can be realized, and a reference is provided for industrially producing the perdeuterated ammonium dinitramide.

Description

technical field [0001] The invention relates to a fully deuterated ammonium dinitramide and a preparation method thereof, belonging to the synthesis technology of deuterated energetic materials. Background technique [0002] Ammonium dinitramide is code-named ADN, which has the characteristics of high oxygen content and high heat of formation, so it can be used as an explosive and is often used as an oxidant for solid propellants. Compared with ammonium perchlorate, the molecular structure of ammonium dinitramide does not contain chlorine, and the combustion product is smokeless, which can increase the concealment of missile launch and reduce environmental pollution. The specific impulse and characteristic velocity of ammonium dinitramide are 2003N s / kg and 1282.6m / s respectively, which are much higher than ammonium perchlorate. By replacing ammonium perchlorate with ammonium dinitramide, the thrust of the aerospace booster can be increased by 14%, and the load can be incre...

Claims

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Application Information

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IPC IPC(8): C01C1/00C06B31/00
CPCC01C1/00C01P2006/10C01P2006/80C06B31/00
Inventor 刘吉平方祝青
Owner BEIJING INSTITUTE OF TECHNOLOGYGY
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