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Небесная энциклопедия

Космические корабли и станции, автоматические КА и методы их проектирования, бортовые комплексы управления, системы и средства жизнеобеспечения, особенности технологии производства ракетно-космических систем

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Применить Всего найдено 4. Отображено 4.
04-05-2011 дата публикации

Preparation method of menthane diamine

Номер: CN0102040525A
Принадлежит:

The invention belongs to the field of chemical synthesis and in particular to a preparation method of menthane diamine. The preparation method comprises the detailed steps: carrying out condensation reaction, hydrolysis reaction, neutralization reaction and purification on bipentene, sulfuric acid and liquid hydrocyanic acid, and then obtaining the menthane diamine. By utilizing the preparation method of menthane diamine, the yield can be up to 82.5% and the purity of the menthane diamine reaches more than 70.0%.

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06-01-2010 дата публикации

Method for preparing N-Phosphonomethyl iminodiacetic acid through hydrolyzing iminodiacetonitrile

Номер: CN0101619077A
Принадлежит:

The invention discloses a method for preparing N-Phosphonomethyl iminodiacetic acid through hydrolyzing iminodiacetonitrile, which comprises the following steps: hydrolyzing and deaminating the iminodiacetonitrile by using lime aqueous solution to obtain solution with the iminodiacetonitrile, acidizing the solution by using hydrochloric acid aqueous solution and sulfuric acid aqueous solution, filtering calcium desulfurization, decoloring filtrate by using active carbon; removing sulfate ions by using barium salt, removing metal ions through an ion-exchange resin column, condensing to obtain solution with iminodiacetic acid salt, reacting with phosphorous acid and formaldehyde under the catalysis of inorganic acid, condensing, crystallizing and filtering reaction solution, respectively collecting filter cakes and filtrate, finally obtaining N-Phosphonomethyl iminodiacetic acid after the filter cakes are dried, and recycling the filtrate. The invention has the advantages of short process ...

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14-07-2010 дата публикации

Method for preparing N-Phosphonomethyl iminodiacetic acid through hydrolyzing iminodiacetonitrile

Номер: CN0101619077B
Принадлежит:

The invention discloses a method for preparing N-Phosphonomethyl iminodiacetic acid through hydrolyzing iminodiacetonitrile, which comprises the following steps: hydrolyzing and deaminating the iminodiacetonitrile by using lime aqueous solution to obtain solution with the iminodiacetonitrile, acidizing the solution by using hydrochloric acid aqueous solution and sulfuric acid aqueous solution, filtering calcium desulfurization, decoloring filtrate by using active carbon; removing sulfate ions by using barium salt, removing metal ions through an ion-exchange resin column, condensing to obtain solution with iminodiacetic acid salt, reacting with phosphorous acid and formaldehyde under the catalysis of inorganic acid, condensing, crystallizing and filtering reaction solution, respectively collecting filter cakes and filtrate, finally obtaining N-Phosphonomethyl iminodiacetic acid after the filter cakes are dried, and recycling the filtrate. The invention has the advantages of short process ...

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20-04-2011 дата публикации

Method for preparing isophorone nitrile

Номер: CN0102020586A
Принадлежит:

The invention relates to the field of chemical synthesis, in particular to a method for preparing isophorone nitrile, which comprises the following concrete steps of: a. reacting isophorone with liquid hydrocyanic acid for 10 minutes to 20 hours at 70-220 DEG C under 1.0-6.0 Mpa under the catalysis of industrial-grade calcium oxide, wherein the mol ratio of isophorone to liquid hydrocyanic acid is 1.2-8.0: 1, and the dosage of the industrial-grade calcium oxide is equivalent to 0.2-10.0 mole percent of the isophorone; b. centrifugalizing or filtering the reaction liquid obtained in the step a to remove the industrial-grade calcium oxide, then distilling for 1-2 times to obtain the crude product of the isophorone nitrile, and recovering an isophorone fraction for application; and c. recrystallizing the crude product of the isophorone nitrile obtained in the step b to obtain the isophorone nitrile. The method can be used for efficiently preparing the higher-purity isophorone nitrile without ...

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