CN211998830U - Continuous sodium azide aqueous phase safety production device - Google Patents

Continuous sodium azide aqueous phase safety production device Download PDF

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Publication number
CN211998830U
CN211998830U CN202020299341.4U CN202020299341U CN211998830U CN 211998830 U CN211998830 U CN 211998830U CN 202020299341 U CN202020299341 U CN 202020299341U CN 211998830 U CN211998830 U CN 211998830U
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reaction
gas
tank
nitrite
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刘湛
刘林学
李建民
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Qingdao Xuejie Chemicals Co ltd
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Qingdao Xuejie Chemicals Co ltd
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Abstract

The utility model discloses a continuous sodium azide aqueous phase safety production device, which comprises a continuous flow microchannel reactor; the continuous flow microchannel reactor is connected with a feed inlet of the gas-liquid separation back pressure tank, a liquid outlet of the gas-liquid separation back pressure tank is connected with a plurality of reaction mixed liquid temporary storage tanks which are connected in parallel, and the plurality of reaction mixed liquid temporary storage tanks which are connected in parallel are connected with a feed inlet of the liquid-liquid separator; the water phase outlet of the liquid-liquid separator is connected with a plurality of reaction mixed liquid concentration crystallization kettles which are connected in parallel, and the bottom valves of the reaction mixed liquid concentration crystallization kettles which are connected in parallel are connected with an automatic centrifuge. The utility model discloses a serialization production method, reaction time shortens to several seconds to several minutes from traditional several hours, and production cycle shortens greatly, and the reaction process safety and stability more is showing and is improving production efficiency.

Description

Continuous sodium azide aqueous phase safety production device
Technical Field
The utility model belongs to the chemical industry field relates to sodium azide, concretely relates to continuous sodium azide aqueous phase safety in production device.
Background
Sodium azide is an important chemical raw material, and is widely used in the fields of medicines, pesticides, electronic products and the like in recent two decades. There are many methods for its synthesis, and the currently industrially commonly used method is the nitrite + hydrazine hydrate + sodium hydroxide method, which is divided into the sulfuric acid + sodium nitrite + alcohol method according to the raw material nitrite synthesis method; dilute nitric acid, sodium nitrite and alcohol method; ammonia oxidation + alcohol process; electrodialysis, etc., different manufacturers choose the process routes according to their capital and specific working conditions, each having advantages and disadvantages. Chinese patents with application numbers 201510629438.0, 201310452735.3, 201510628267.X, 201721146705.X and 201310451461.6 respectively disclose synthesis processes of sodium azide and raw material nitrite thereof, wherein sodium azide is synthesized into methyl ester, ethyl ester, propyl ester, butyl ester and isoamyl ester which are used in industry, ethyl ester (boiling point of ethyl nitrite is 17 ℃) is used in one step, methyl ester is low in cost but is difficult to control due to toxic gas intermittent operation, and excessive tail gas is difficult to recover to cause environmental problems, and propyl ester, butyl ester and isoamyl ester are high in cost and are rarely adopted due to pungent odor in production environment. In the nitridization step, methanol is generally used as a solvent due to the solubility problem of sodium hydroxide, and ethanol is adopted secondly. The ethanol is adopted as a solvent to be matched with ethyl nitrite for post-treatment, but the ethanol has high cost, more importantly, the solubility of sodium azide in the ethanol is 0.3 percent at 25 ℃, impurities are easy to wrap, so that the product is impure and the free alkali is high. Therefore, many industrial manufacturers can produce qualified products by using ethyl nitrite as a raw material and methanol as a solvent at one time, the total cost is low, but the problem of separating methanol from ethanol exists in the post-treatment.
The Chinese patent with the application number of 201210132140.5 discloses a preparation method of sodium azide, wherein ethyl nitrite gas is introduced into a mixture consisting of hydrazine hydrate, sodium hydroxide, a catalyst and ethanol, and after the introduction of the gas is finished, the reaction is carried out for 1.5 to 2.5 hours at the temperature of 18 to 25 ℃. The catalyst is one of benzyltriethylammonium chloride, tributylamine, tetrabutylammonium bromide, tetrabutylammonium chloride, tetrabutylammonium hydrogen sulfate, trioctylmethylammonium chloride, dodecyltrimethylammonium chloride, tetradecyltrimethylammonium chloride and quaternary ammonium base. The ethanol in the technical scheme can be recycled, but the method is a gas-liquid two-phase synthesis process, needs high-pressure operation, has the risk of gas leakage and has strict condition control. From the current production practice, the main problem of the azidation reaction is the safety problem, because sodium azide is an explosive and extremely toxic chemical, the used raw materials of nitrite and hydrazine are extremely toxic and flammable liquids, the used solvents of methanol and ethanol are flammable and toxic liquids, the reaction heat effect is extremely large and easy to lose control, multiple industrial explosion and casualty accidents of poisoning are reported, and in order to solve the problems, a water phase synthesis method is adopted, so that on one hand, the product impurity caused by the solubility problem of sodium hydroxide and sodium azide can be avoided, the productivity can be improved, the byproduct alcohol is singly and easily separated, more importantly, the water phase reaction is safe, and the cost is low. However, the solubility of nitrite in water is poor, which results in low reaction rate, low conversion rate and low product purity.
Chinese patent No. 201210140899.8 discloses a water phase synthesis method of sodium azide, which comprises adding liquid ethyl nitrite into a reaction system composed of hydrazine hydrate, sodium hydroxide, a phase transfer catalyst and water, carrying out a closed reaction, recovering unreacted ethyl nitrite, by-products ethanol and water after the reaction is completed, and then filtering the reaction solution to obtain sodium azide. Because the reaction heat effect is relatively large, the liquid ethyl nitrite with low boiling point is used as the raw material to carry out one-time feeding reaction in the batch reactor, and the one-time feeding reaction is easy to be out of control, so that the system pressure is increased and the system is exploded.
The application number 201510114085.0 discloses a sodium azide aqueous phase synthesis process for recycling n-butyl alcohol, which comprises the steps of mixing butyl nitrite, sodium hydroxide, hydrazine hydrate, a catalyst and water to form a reaction system, recovering n-butyl alcohol after the reaction is finished, filtering to obtain sodium azide, recycling the recovered n-butyl alcohol, and using n-butyl ester with a high boiling point (the boiling point is 78 ℃) which is relatively safe. However, the reaction time is as long as 12 hours due to poor water solubility of butyl nitrite, the product purity is low, and the generated n-butanol has bad smell and is not friendly to the production environment.
Disclosure of Invention
Not enough to prior art exists, the utility model aims to provide a continuous sodium azide aqueous phase safety in production device, solve among the prior art sodium azide and be difficult to promote production technology and security comprehensively when producing, lead to being difficult to satisfy the technical problem of the requirement of industrial production practice.
In order to solve the technical problem, the utility model discloses a following technical scheme realizes:
a continuous sodium azide aqueous phase safety production device comprises a nitrite high-level tank and a hydrazine hydrate and sodium hydroxide aqueous solution high-level tank, wherein the nitrite high-level tank is connected with a continuous flow microchannel reactor through a compressor or a metering pump, and the hydrazine hydrate and sodium hydroxide aqueous solution high-level tank is connected with the continuous flow microchannel reactor through the metering pump;
the continuous flow microchannel reactor is connected with a feed inlet of a gas-liquid separation back pressure tank, a gas outlet of the gas-liquid separation back pressure tank is connected with a gas cooling absorption tank which is connected in series in multiple stages, a liquid outlet of the gas-liquid separation back pressure tank is connected with a plurality of reaction mixed liquid temporary storage tanks which are connected in parallel, and the plurality of reaction mixed liquid temporary storage tanks which are connected in parallel are connected with a feed inlet of a liquid-liquid separator;
the organic phase outlet of the liquid-liquid separator is connected with the ester and alcohol recovery tank, the water phase outlet of the liquid-liquid separator is connected with a plurality of reaction mixed liquid concentration crystallization kettles which are connected in parallel, and the bottom valves of the reaction mixed liquid concentration crystallization kettles which are connected in parallel are connected with an automatic centrifuge.
The utility model discloses still have following technical characteristic:
the continuous flow microchannel reactor, the gas-liquid separation back pressure tank and the multistage series gas cooling absorption tanks are all provided with a cooling liquid inlet and a cooling liquid outlet.
The multistage gas cooling absorption tank that establishes ties be the two-stage, a plurality of parallelly connected reaction mixture jar of keeping in and a plurality of parallelly connected reaction mixture concentration crystallization kettle are more than two.
The continuous sodium azide aqueous phase safe production process adopts the continuous sodium azide aqueous phase safe production device.
Specifically, the molar ratio of the raw material, namely nitrite to hydrazine hydrate to sodium hydroxide is 1.05-2.5:
1.05-1.2: 1.0, the residence time in the continuous flow microchannel reactor is 10-350 seconds, the reaction temperature is 10-95 ℃, and the reaction pressure is 0.1-10 Mpa.
Specifically, the nitrite comprises methyl nitrite, ethyl nitrite, propyl nitrite, isopropyl nitrite, n-butyl nitrite, isobutyl nitrite or isoamyl nitrite.
Preferably, the molar ratio of the raw material of the nitrous acid ester to the hydrazine hydrate to the sodium hydroxide is 1.3-1.5:
1.05: 1.0, the residence time in the continuous flow microchannel reactor is 50-100 seconds, the reaction temperature is 30-50 ℃, and the reaction pressure is 2-8 Mpa.
The continuous flow microchannel reactor (5) comprises a modular micro-reactor or a tube bundle micro-reactor.
The microchannel structure of the modular microreactor comprises a direct-current channel, a flat pipeline with a rectangular cross section, a pulse variable-diameter rectangular flat pipeline and a channel of a Heart Cell structure of Corning;
the pulse variable-diameter rectangular flat pipeline comprises a round cake type pulse variable-diameter rectangular flat pipeline, an oblique square cake type pulse variable-diameter rectangular flat pipeline, a reinforced mixed type round cake type rectangular flat pipeline or a reinforced mixed type oblique square cake type rectangular flat pipeline;
the tube bundle type microreactor is characterized in that the internal flow channel of the tube bundle type microreactor is in a rectangular microchannel form.
Compared with the prior art, the utility model, following technological effect has:
(I) the utility model discloses a serialization production method, reaction time shortens to several seconds to several minutes from traditional several hours, and production cycle shortens greatly, and the reaction process is safety and stability more, is showing and is improving production efficiency.
(II) because the continuous flow microchannel reactor has the structural characteristics of small reaction space and huge specific surface area, the mass transfer and heat transfer in the reaction process can be strengthened, thereby the two-phase reaction system can be fully carried out to complete the reaction in the water phase, the occupied area of the whole reaction system is small, and the equipment investment is reduced.
(III) the utility model discloses can make the reaction keep going on under certain pressure stops the high pressure very much, make low cost's methyl nitrite, ethyl ester reaction safer, more thorough, thereby need not phase transfer catalyst and make the product purer, the cost is lower.
(IV) the whole system adopts continuous and closed operation, so that the solvent loss and the pollution of VOCs are avoided.
(V) the utility model can design safe production scale through the quantity of the continuous flow micro-channel reactor, the raw material feeding speed control, the system reaction pressure adjustment, etc., or flexibly arrange the production quantity, and completely realize automation.
Drawings
FIG. 1 is a schematic connection diagram of the continuous sodium azide aqueous phase safety production apparatus of the present invention.
The meaning of the individual reference symbols in the figures is: the device comprises a 1-nitrite ester high-level tank, a 2-hydrazine hydrate and sodium hydroxide aqueous solution high-level tank, a 3-compressor or a metering pump, a 4-metering pump, a 5-continuous flow microchannel reactor, a 6-gas-liquid separation back pressure tank, a 7-multistage series gas cooling absorption tank, 8-a plurality of parallel reaction mixed liquid temporary storage tanks, 9-a liquid-liquid separator, a 10-ester and alcohol recovery tank, 11-a plurality of parallel reaction mixed liquid concentration crystallization kettles and 12-an automatic centrifuge.
The following examples are provided to explain the present invention in further detail.
Detailed Description
As can be seen from the analysis of the prior art in the background art, the sodium azide production process mainly has four problems, namely, the safety problem, and the safety production is determined to be the first concern because the reaction heat effect is large and the used raw materials and products are inflammable, explosive and highly toxic; secondly, the reaction speed, the conversion rate and the product purity are problems, because the sodium azide purification can only be realized through the conversion and the purification of the virulent hydrazoic acid, the danger is high, and the purification method is rarely adopted in a factory, so the application of a water phase method is influenced; the third aspect is the cost issue, and the presently disclosed processes all attempt to reduce production costs; the fourth aspect is the universal problem of the reported process method, namely the continuous and automatic problem of the reaction process, the problems of safety, cost, production efficiency and the like are solved. Therefore, the solution of the above problems becomes the goal of the technicians engaged in the production of sodium azide, so that no comprehensive solution is found at present, and the existing reports provide a targeted method for the problems of a certain aspect, but bring new disadvantages and cannot meet the requirements of production practice.
The utility model provides a to the not enough of above technology existence, proposed on aqueous phase method basis and adopted the microchannel reactor to react the aqueous solution of nitrite and hydrazine hydrate and sodium hydroxide and generate the technology of sodium azide. The method can strictly control the temperature and the residence time in the reaction process, prevent the reaction from being out of control, and improve the safety of the production process. The utility model can continuously, safely and efficiently carry out gas-liquid and liquid-liquid two-phase reactions due to the strong mass transfer and heat transfer functions of the microchannel reactor and the strong bearing capacity of the reactor. The microchannel reactor has the structural characteristics of small reaction space and large specific surface area, so that mass transfer and heat transfer in the reaction process can be enhanced, reaction heat can be led out to the maximum extent and possibly utilized, the reaction can be kept at a certain pressure even under high pressure, gas-liquid and liquid-liquid two phases can be continuously and fully and quickly reacted, continuous automatic production can be realized, the reactor can be stopped at any time, and the production scale can be flexibly designed and arranged by controlling the raw material feeding speed, adjusting the reaction pressure of the system and the like. The process effectively, safely and comprehensively solves the technical problems of sodium azide and can realize continuous automatic production.
The utility model discloses a continuous flow microchannel reactor, with nitrite and the hydrazine hydrate that prepares, sodium hydroxide aqueous solution measure respectively and let in the reactor according to certain proportion, the reaction obtains sodium azide aqueous solution under certain temperature, certain pressure, this solution is through distilling (or liquid-liquid separation) retrieve excessive ester and the alcohol of production, concentration, centrifugal separation, drying obtain sodium azide finished product, the alcohol of retrieving and ester return system ester workshop section and apply mechanically, distilled water, mother liquor are applied mechanically.
In the present invention, all the components of the device are known products unless otherwise specified.
The utility model discloses in, the gaseous tail gas processing workshop section that goes of top of the gas cooling adsorption tanks of multistage series connection. The absorption liquid returns to the prepared hydrazine and sodium hydroxide solution for reuse.
In the utility model, the liquid-liquid separator is only used for the condition that the generated byproduct alcohol is insoluble in water, and the separated organic phase is the mixture of alcohol and excessive ester and returns to the ester production section for application.
The utility model discloses in, the preceding fraction that the top of a plurality of parallelly connected reaction mixture liquid concentration crystallization kettle was gone out removes ester preparation workshop section and uses mechanically, and the batching workshop section is removed to the distilled water.
The utility model discloses in, the mother liquor among the automatic centrifuge returns the batching workshop section after handling, and the product removes dry finished product workshop section.
The following embodiments of the present invention are given, and it should be noted that the present invention is not limited to the following embodiments, and all the equivalent transformations made on the basis of the technical solution of the present application all fall into the protection scope of the present invention.
Example 1:
following the above technical solution, as shown in fig. 1, this embodiment provides a continuous sodium azide aqueous phase safety production apparatus, which includes a nitrite high-level tank 1 and a hydrazine hydrate and sodium hydroxide aqueous solution high-level tank 2, and is characterized in that the nitrite high-level tank 1 is connected to a continuous flow microchannel reactor 5 through a compressor or a metering pump 3, and the hydrazine hydrate and sodium hydroxide aqueous solution high-level tank 2 is connected to the continuous flow microchannel reactor 5 through a metering pump 4;
the continuous flow microchannel reactor 5 is connected with a feed inlet of a gas-liquid separation back pressure tank 6, a gas outlet of the gas-liquid separation back pressure tank 6 is connected with a gas cooling absorption tank 7 which is connected in series in multiple stages, a liquid outlet of the gas-liquid separation back pressure tank 6 is connected with a plurality of reaction mixed liquid temporary storage tanks 8 which are connected in parallel, and the plurality of reaction mixed liquid temporary storage tanks 8 which are connected in parallel are connected with a feed inlet of a liquid-liquid separator 9;
an organic phase outlet of the liquid-liquid separator 9 is connected with an ester and alcohol recovery tank 10, a water phase outlet of the liquid-liquid separator 9 is connected with a plurality of reaction mixed liquid concentration crystallization kettles 11 which are connected in parallel, and bottom valves of the reaction mixed liquid concentration crystallization kettles 11 which are connected in parallel are connected with an automatic centrifuge 12.
As a preferable scheme of this embodiment, the continuous flow microchannel reactor 5, the gas-liquid separation back pressure tank 6 and the multistage series gas cooling absorption tank 7 are all provided with a cooling liquid inlet and a cooling liquid outlet.
In a preferred embodiment of the present invention, the gas cooling absorption tank 7 connected in series in multiple stages has two stages, and each of the reaction mixed liquid temporary storage tank 8 and the reaction mixed liquid concentration crystallization kettle 11 connected in parallel is two or more.
Example 2:
this example provides a continuous sodium azide aqueous phase safety process that employs the continuous sodium azide aqueous phase safety apparatus of example 1.
Specifically, the nitrite is methyl nitrite, and the temperature of the nitrite head tank 1 is normal temperature.
Specifically, the concentration of sodium hydroxide was 20 wt.%.
The prepared hydrazine and NaOH mixed solution enters a mixed reaction zone through a metering pump 4, methyl nitrite enters the mixed reaction zone through a compressor 3 through a flowmeter, the reaction residence time is controlled to be 50s by adjusting the flow and the channel length of a continuous flow microchannel reactor 5, and the molar ratio of the methyl nitrite to the hydrazine hydrate and the sodium hydroxide is controlled to be 1.3: 1.05: 1.0, setting the reaction temperature to be 30 ℃, the reaction pressure of the system to be 5.0MPa and the gas-liquid separation temperature to be 30 ℃. And (3) continuously discharging excessive methyl nitrite and reaction mixed solution from the reaction mixture entering a gas-liquid separation back pressure tank 6, absorbing the methyl nitrite by hydrazine hydrate and sodium hydroxide mixed solution, mechanically applying the absorption solution during burdening, and distilling, concentrating, crystallizing, separating and drying the reaction mixed solution to obtain a solid powder finished product. By analyzing the main content of 99.1 percent and free alkali of 0.5 percent, the distilled methanol returns to an ester preparation working section, and the distilled water and the mother liquor of the centrifuge return to a material preparation working section to prepare the mixed solution of hydrazine and sodium hydroxide.
Example 3:
this example provides a continuous sodium azide aqueous phase safety process that employs the continuous sodium azide aqueous phase safety apparatus of example 1.
Specifically, the nitrite is gaseous ethyl nitrite, and the temperature of the nitrite head tank 1 is normal temperature.
Specifically, the concentration of sodium hydroxide was 20 wt.%.
The prepared hydrazine and NaOH mixed solution enters a mixed reaction zone through a metering pump 4, the ethyl nitrite enters the mixed reaction zone through a compressor 3 through a flowmeter, the reaction residence time is controlled to be 80s by adjusting the flow and the channel length of a continuous flow microchannel reactor 5, and the molar ratio of the ethyl nitrite to the hydrazine hydrate to the sodium hydroxide is controlled to be 1.3: 1.05: 1.0, setting the reaction temperature at 50 ℃, the reaction pressure of the system at 8.0MPa and the gas-liquid separation temperature at 50 ℃. And (3) continuously discharging excessive ethyl nitrite and reaction mixed solution from the reaction mixture in a gas-liquid separation back pressure tank 6, absorbing the ethyl nitrite by hydrazine hydrate and sodium hydroxide mixed solution, mechanically applying the absorption solution during burdening, and distilling, concentrating, crystallizing, separating and drying the reaction mixed solution to obtain a solid powder finished product. By analyzing the main content of 99.5 percent and free alkali of 0.3 percent, the distilled ethanol returns to an ester preparation working section, and the distilled water and the centrifuge mother liquor return to a material preparation working section to prepare the mixed solution of hydrazine and sodium hydroxide.
Example 4:
this example provides a continuous sodium azide aqueous phase safety process that employs the continuous sodium azide aqueous phase safety apparatus of example 1.
Specifically, the nitrite is liquid ethyl nitrite, and the temperature of the nitrite head tank 1 is 10 ℃.
Specifically, the concentration of sodium hydroxide was 20 wt.%.
The prepared hydrazine and NaOH mixed solution enters a mixed reaction zone through a metering pump 4, the ethyl nitrite enters the mixed reaction zone through the metering pump 3 through a flowmeter, the reaction residence time is controlled to be 100s by adjusting the flow and the channel length of a continuous flow microchannel reactor 5, and the molar ratio of the ethyl nitrite to the hydrazine hydrate to the sodium hydroxide is controlled to be 1.3: 1.05: 1.0, setting the reaction temperature to be 35 ℃, the reaction pressure of the system to be 3.0MPa and the gas-liquid separation temperature to be 35 ℃. And (3) continuously discharging excessive ethyl nitrite and reaction mixed solution from the reaction mixture in a gas-liquid separation back pressure tank 6, absorbing the ethyl nitrite by hydrazine hydrate and sodium hydroxide mixed solution, mechanically applying the absorption solution during burdening, and distilling, concentrating, crystallizing, separating and drying the reaction mixed solution to obtain a solid powder finished product. By analyzing the main content of 99.5 percent and free alkali of 0.3 percent, the distilled ethanol returns to an ester preparation working section, and the distilled water and the centrifuge mother liquor return to a material preparation working section to prepare the mixed solution of hydrazine and sodium hydroxide.
Example 5:
this example provides a continuous sodium azide aqueous phase safety process that employs the continuous sodium azide aqueous phase safety apparatus of example 1.
Specifically, the nitrite is isopropyl nitrite, and the temperature of the nitrite head tank 1 is normal temperature.
Specifically, the concentration of sodium hydroxide was 20 wt.%.
The prepared hydrazine and NaOH mixed solution enters a mixed reaction zone through a metering pump 4, the isopropyl nitrite enters the mixed reaction zone through the metering pump 3 through a flow meter, the reaction residence time is controlled to be 80s by adjusting the flow and the channel length of a continuous flow microchannel reactor 5, and the molar ratio of the isopropyl nitrite to the hydrazine hydrate and the sodium hydroxide is controlled to be 1.5: 1.05: 1.0, setting the reaction temperature to be 40 ℃, the reaction pressure of the system to be 2.0MPa and the gas-liquid separation temperature to be 20 ℃. And the reaction mixture enters a gas-liquid separation back pressure tank 6 to continuously discharge excessive isopropyl nitrite and reaction mixed solution, the tail gas of the isopropyl nitrite is absorbed by the mixed solution of hydrazine hydrate and sodium hydroxide, the absorption solution is applied mechanically during batching, and the reaction mixed solution is subjected to distillation, concentration, crystallization, separation and drying to obtain a solid powder finished product. By analyzing the main content of 99.5 percent and the free alkali of 0.3 percent, the distilled isopropanol and isopropyl ester are returned to the ester preparation working section, and the distilled water and the mother liquor of the centrifuge are returned to the ingredient preparation working section to prepare the mixed liquid of hydrazine and sodium hydroxide.
Example 6:
this example provides a continuous sodium azide aqueous phase safety process that employs the continuous sodium azide aqueous phase safety apparatus of example 1.
Specifically, the nitrite is n-butyl nitrite, and the temperature of the nitrite head tank 1 is normal temperature.
Specifically, the concentration of sodium hydroxide was 20 wt.%.
The prepared hydrazine and NaOH mixed solution enters a mixed reaction zone through a metering pump 4, the n-butyl nitrite enters the mixed reaction zone through the metering pump 3 through a flowmeter, the reaction residence time is controlled to be 80s by adjusting the flow and the channel length of a continuous flow microchannel reactor 5, and the molar ratio of the n-butyl nitrite to the hydrazine hydrate to the sodium hydroxide is controlled to be 1.5: 1.05: 1.0, setting the reaction temperature to be 50 ℃, the reaction pressure of the system to be 2.0MPa and the gas-liquid separation temperature to be 50 ℃. And (3) continuously discharging excessive n-butyl nitrite and reaction mixed solution from the reaction mixture in a gas-liquid separation back pressure tank 6, absorbing n-butyl nitrite tail gas by hydrazine hydrate and sodium hydroxide mixed solution, mechanically applying the absorption solution during burdening, and distilling, concentrating, crystallizing, separating and drying the reaction mixed solution to obtain a solid powder finished product. After analysis, the main content is 99.5 percent, the free alkali is 0.3 percent, the distilled n-butyl alcohol and the n-butyl nitrite are returned to the ester preparation working section, and the distilled water and the mother liquor of the centrifuge are returned to the ingredient preparation working section to prepare the mixed solution of hydrazine and sodium hydroxide.
Example 7:
this example provides a continuous sodium azide aqueous phase safety process that employs the continuous sodium azide aqueous phase safety apparatus of example 1.
Specifically, the nitrite is isoamyl nitrite, and the temperature of the nitrite head tank 1 is normal temperature.
Specifically, the concentration of sodium hydroxide was 20 wt.%.
The prepared hydrazine and NaOH mixed solution enters a mixed reaction zone through a metering pump 4, isoamyl nitrite enters the mixed reaction zone through the metering pump 3 through a flowmeter, the reaction residence time is controlled to be 80s by adjusting the flow and the channel length of a continuous flow microchannel reactor 5, and the molar ratio of the isoamyl nitrite to the hydrazine hydrate to the sodium hydroxide is controlled to be 1.5: 1.05: 1.0, setting the reaction temperature to be 50 ℃, the reaction pressure of the system to be 2.0MPa and the gas-liquid separation temperature to be 50 ℃. The reaction mixture enters a gas-liquid separation back pressure tank 6 to continuously discharge excessive isoamyl nitrite and reaction mixed solution, isoamyl nitrite tail gas is absorbed by hydrazine hydrate and sodium hydroxide mixed solution, and absorption solution is indiscriminately used during burdening. Separating organic phase and water phase from the reaction mixed solution by a liquid-liquid separator, returning the organic phase to the ester preparation working section, and distilling, concentrating, crystallizing, separating and drying the water phase to obtain a solid powder finished product. By analysis, the main content is 99.5%, the free alkali is 0.3%, and the distilled water and the mother liquor of the centrifuge are returned to the material preparation section to prepare the mixed liquor of hydrazine and sodium hydroxide.

Claims (3)

1. A continuous sodium azide aqueous phase safety production device comprises a nitrite high-level tank (1) and a hydrazine hydrate and sodium hydroxide aqueous solution high-level tank (2), and is characterized in that the nitrite high-level tank (1) is connected with a continuous flow microchannel reactor (5) through a compressor or a metering pump (3), and the hydrazine hydrate and sodium hydroxide aqueous solution high-level tank (2) is connected with the continuous flow microchannel reactor (5) through a metering pump (4);
the continuous flow microchannel reactor (5) is connected with a feed inlet of a gas-liquid separation back pressure tank (6), a gas outlet of the gas-liquid separation back pressure tank (6) is connected with a gas cooling absorption tank (7) which is connected in series in multiple stages, a liquid outlet of the gas-liquid separation back pressure tank (6) is connected with a plurality of reaction mixed liquid temporary storage tanks (8) which are connected in parallel, and the plurality of reaction mixed liquid temporary storage tanks (8) which are connected in parallel are connected with a feed inlet of a liquid-liquid separator (9);
an organic phase outlet of the liquid-liquid separator (9) is connected with an ester and alcohol recovery tank (10), a water phase outlet of the liquid-liquid separator (9) is connected with a plurality of reaction mixed liquid concentration crystallization kettles (11) which are connected in parallel, and bottom valves of the reaction mixed liquid concentration crystallization kettles (11) which are connected in parallel are connected with an automatic centrifuge (12).
2. The continuous safe production device of sodium azide aqueous phase according to claim 1, wherein the continuous flow microchannel reactor (5), the gas-liquid separation back pressure tank (6) and the multistage series gas cooling absorption tank (7) are provided with a cooling liquid inlet and a cooling liquid outlet.
3. The continuous production apparatus for sodium azide aqueous phase safety as claimed in claim 1, wherein the multistage series gas cooling absorption tank (7) is two-stage, and the number of the reaction mixture temporary storage tanks (8) and the number of the reaction mixture concentration crystallization tanks (11) are two or more.
CN202020299341.4U 2020-03-11 2020-03-11 Continuous sodium azide aqueous phase safety production device Withdrawn - After Issue CN211998830U (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111252746A (en) * 2020-03-11 2020-06-09 青岛雪洁助剂有限公司 Continuous sodium azide water-phase safe production device and process

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111252746A (en) * 2020-03-11 2020-06-09 青岛雪洁助剂有限公司 Continuous sodium azide water-phase safe production device and process
CN111252746B (en) * 2020-03-11 2023-05-16 青岛雪洁助剂有限公司 Continuous sodium azide water phase safety production device and process

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