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Hydrolysis technology and device for concentrated hydrochloric acid

A concentrated acid hydrolysis and hydrolysis device technology, applied in organic chemistry, silicon organic compounds, chemical instruments and methods, etc., can solve problems affecting the normal operation of equipment, unfavorable oil-water separation, and decrease in ring yield, so as to improve reaction efficiency and product quality, improved separation, and reduced coagulation

Active Publication Date: 2017-01-11
HUBEI XINGFA CHEM GRP CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The disadvantage of azeotropic acid hydrolysis is that the hydrogen chloride molecules generated by the hydrolysis reaction have a high heat of solution in dilute acid. In order to prevent the hydrolysis temperature from being too high, a large amount of cooling capacity is required for cooling; The reboiler needs to consume a lot of heat; the hydrolyzate entrained in the concentrated acid will also self-accumulate and settle in the desorption column, forming a jelly, which affects the normal operation of the equipment
However, the concentrated acid hydrolysis process still has the following deficiencies: (1) In the current technological process, static mixers are mainly used as hydrolysis reactors, but the materials in the static mixers cannot be deeply mixed on the molecular scale, resulting in the localization of the materials in the reaction system. Excessive, resulting in a decrease in the yield of cyclic bodies in the hydrolyzate, resulting in more short-chain linear bodies with hydrophilic hydroxyl groups at the chain ends. The linear bodies have a certain degree of hydrophilicity and hydrophobicity at the same time, so it is easy to emulsify in the water separator and not It is beneficial to the separation of oil and water, and is easily carried by hydrogen chloride gas, and is easy to self-polymerize, forming a jelly in the methyl chloride synthesis section; (2) under the existing process conditions, the hydrogen chloride gas produced from the top of the gas-liquid separation tank is condensed The diameter of the post-condensate droplet is still smaller than the effective treatment diameter of the demister (3-5 μm), and the demister cannot completely remove the hydrolyzate carried in the hydrogen chloride gas

Method used

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  • Hydrolysis technology and device for concentrated hydrochloric acid

Examples

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Comparison scheme
Effect test

Embodiment 1

[0018] Control the hydrolysis reaction between dimethyldichlorosilane and concentrated hydrochloric acid in a static mixer at 35°C and 0.2MPa, and the resulting gas-liquid mixture enters the gas-liquid separation tank A (1) for separation, and the gas-liquid separation tank A (1 ) The gas produced at the top enters the Venturi mixer (2) and is fully mixed with the concentrated hydrochloric acid main fluid. The mass concentration of the concentrated hydrochloric acid is 38%, and the mass ratio of the concentrated acid to the gas mixture is 1:3. The gas-liquid separation tank B (3) is separated, the liquid extracted from the bottom of the gas-liquid separation tank B (3) is returned to the Venturi mixer through the material pump, and the gas extracted from the top is passed through the primary condenser (4) and the secondary condenser (5) The final temperature is -10°C and the pressure is 0.15MPa. The liquid extracted from the bottom of the gas-liquid separation tank (1) and the...

Embodiment 2

[0020] Control the hydrolysis reaction between dimethyldichlorosilane and concentrated hydrochloric acid in a static mixer at 35°C and 0.2MPa, and the resulting gas-liquid mixture enters the gas-liquid separation tank A (1) for separation, and the gas-liquid separation tank A (1 ) The gas produced at the top enters the Venturi mixer (2) and is fully mixed with the concentrated hydrochloric acid main fluid. The mass concentration of the concentrated hydrochloric acid is 38%, and the mass ratio of the concentrated acid to the gas mixture is 1:4. The gas-liquid separation tank B (3) is separated, the liquid extracted from the bottom of the gas-liquid separation tank B (3) is returned to the Venturi mixer through the material pump, and the gas extracted from the top is passed through the primary condenser (4) and the secondary condenser (5) The final temperature is 0°C and the pressure is 0.20MPa. The liquid extracted from the bottom of the gas-liquid separation tank (1) and the c...

Embodiment 3

[0022] Control the hydrolysis reaction between dimethyldichlorosilane and concentrated hydrochloric acid in a static mixer at 35°C and 0.2MPa, and the resulting gas-liquid mixture enters the gas-liquid separation tank A (1) for separation, and the gas-liquid separation tank A (1 ) The gas produced at the top enters the Venturi mixer (2) and is fully mixed with the concentrated hydrochloric acid main fluid. The mass concentration of the concentrated hydrochloric acid is 38%, and the mass ratio of the concentrated acid to the gas mixture is 1:5. The gas-liquid separation tank B (3) is separated, the liquid extracted from the bottom of the gas-liquid separation tank B (3) is returned to the Venturi mixer through the material pump, and the gas extracted from the top is passed through the primary condenser (4) and the secondary condenser (5) The final temperature is 10°C and the pressure is 0.25MPa. The liquid extracted from the bottom of the gas-liquid separation tank (1) and the ...

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Abstract

The invention provides a concentrated-acid hydrolysis technology. The concentrated-acid hydrolysis technology includes the steps that after hydrolysis raw materials of dimethyldichlorosilane and saturated concentrated hydrochloric acid are reacted in a static mixer, the obtained gas-liquid mixture enters a gas-liquid separation tank A, gas recovered out of the top of the gas-liquid separation tank A, carried dimethyldichlorosilane and carried hydrolysate liquid drops enter a venturi mixer from the side face, the gas-liquid mixture deeply mixed in a main concentrated-hydrochloric-acid fluid enters a gas-liquid separation tank B, concentrated hydrochloric acid recovered out of the bottom of the gas-liquid separation tank B is returned to the venturi mixer through a material pump, the gas recovered out of the top sequentially enters a primary condenser and a secondary condenser, gas-liquid mixture condensed by the primary condenser and the secondary condenser enters a collecting device to collect liquid drops, and after the liquid drops are removed through a demister, the product is delivered to a chloromethane synthesis working section through a buffering tank. By means of the concentrated-acid hydrolysis technology, in the concentrated-acid hydrolysis process, the insufficient reacting problem, the low efficiency problem and the like caused when materials are unevenly mixed are solved, and meanwhile the problems that as gas and liquid are carried, a pipe and a device are blocked are solved.

Description

technical field [0001] The invention relates to a high-efficiency concentrated acid hydrolysis process, which belongs to the technical field of organosilicon hydrolyzate production. Background technique [0002] The hydrolysis of dimethyldichlorosilane can use azeotropic acid with a mass fraction of 21%-22% as a raw material. After the hydrolysis reaction, the mixture is separated by a water separator. The upper layer is the product hydrolyzate, which enters the cracking section after being boiled and neutralized. The lower layer is the by-product concentrated hydrochloric acid, which enters the hydrogen chloride desorption tower to decompose hydrogen chloride gas for the synthesis of methyl chloride. The disadvantage of azeotropic acid hydrolysis is that the hydrogen chloride molecules generated by the hydrolysis reaction have a high heat of solution in dilute acid. In order to prevent the hydrolysis temperature from being too high, a large amount of cooling capacity is req...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07F7/08C07F7/18C08G77/04
CPCC07F7/08C07F7/18C08G77/045
Inventor 李书兵颜昌锐聂亮王文金张浩
Owner HUBEI XINGFA CHEM GRP CO LTD
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