Continuous production method of epoxy chloropropane by hydrogen peroxide process

A technology of epichlorohydrin and its production method, which is applied in the direction of organic chemistry, can solve the problems of increasing catalyst regeneration frequency and cost, cost increase, low recovery rate, etc., and achieve activity and epoxidation selectivity maintenance and smooth operation control , Improve the effect of unit production capacity

Active Publication Date: 2009-07-15
JIANGSU YANGNONG CHEM GROUP +2
View PDF3 Cites 43 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Due to the absence of solvent, the activity of the catalyst decreases rapidly and the life is short, which is not conducive to the recycling of the catalyst, and also increases the frequency and cost of catalyst regeneration
[0008] To sum up, there are existing methods for continuous preparation of epichlorohydrin. ①A fixed-bed or trickle-bed reactor is used to realize continuous material, and the reaction liquid phase material must be homogeneous, so the amount of solvent used is large and the separation capacity is high. The consumption is high, allyl chloride and epichlorohydrin are directly separated from a large amount of methanol and water by atmospheric distillation, and the by-products will increase if the temperature is above 50 °C, and the separation yield of epichlorohydrin is low; if negative pressure distillation is used for separation, The loss of allyl chloride is large, the recovery rate is low, and the cost increases; if an extractant is used, new components will be introduced and the complexity of the process will be increased
2. Kettle type or supergravity continuous reaction does not use new solvents, directly using chloropropene not only as the reaction raw material, but also as the reaction solvent will cause: on the one hand, alcohol, ketone, etc. are not used as solvents, and the catalyst is in the liquid phase (chloropropene and hydrogen peroxide) ) has high surface tension and poor dispersion performance. On the other hand, it is not conducive to the diffusion of reaction products in the catalyst pores, the catalyst activity decreases rapidly, the service life is short, and the catalyst regeneration frequency and use cost increase.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Continuous production method of epoxy chloropropane by hydrogen peroxide process
  • Continuous production method of epoxy chloropropane by hydrogen peroxide process
  • Continuous production method of epoxy chloropropane by hydrogen peroxide process

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0021] Three kettles are connected in series, the effective volume of each kettle: 130mL, 270mL, 230mL, the total effective volume is 630mL, the reaction temperature is 41-49℃, the reaction is exothermic, and the heat is exchanged through the jacket. Catalyst with 27.5% H 2 o 2 The mass ratio is 1:12. Allyl chloride (AC) and H 2 o 2 Use a peristaltic pump to drive into the first-stage reaction kettle at the same time, and the flow rates are V AC =167.1mL / hr, V H2O2 =87.0mL / hr, methanol and catalyst are mixed evenly and beating with peristaltic pump to control feeding, V MA =165.9 mL / hr. The stirring speed is 350rpm, the three reactors stay for about 1.5hr, the feed flow rate per hour is 420mL / h, and the reaction materials overflow from the upper end of the reactor and enter the next reactor.

[0022]After the reaction is over, the aqueous phase catalyst slurry is separated by membrane filtration, and the catalyst filter cake or concentrated slurry is directly beaten wit...

Embodiment 2

[0027] Three kettles are connected in series, the effective volume of each kettle: 130mL, 270mL, 230mL, the total effective volume is 630mL, the reaction temperature is 41-49℃, the reaction is exothermic reaction, and the heat is exchanged through the jacket. Catalyst with 35% H 2 o 2 The mass ratio is 1:10. AC and H 2 o 2 Use a peristaltic pump at a certain flow rate to drive into the first-stage reactor at the same time, and the flow rates are V AC =167.1mL / hr, V H2O2 =87.0mL / hr, methanol and catalyst are mixed evenly and beating with peristaltic pump to control feeding, V MA =165.9 mL / hr. The three kettles stay for about 1.5hr, the feed flow rate per hour = 420mL / h, the stirring speed is 350rpm, and the reaction material overflows from the upper end of the reactor and enters the next reactor.

[0028] After the reaction is over, the aqueous phase catalyst slurry is separated by membrane filtration, and the catalyst filter cake or concentrated slurry is directly beate...

Embodiment 3

[0032] Single tank continuous operation, the effective volume of the tank: 500mL. Mixed slurry of methanol and catalyst, AC and H 2 o 2 Use a peristaltic pump to feed from the bottom of the reaction tank at a certain flow rate, the flow rate of the mixed slurry of catalyst and methanol is 90mL / hr, allyl chloride and 50%H 2 o 2 The flow rates are: 187mL / hr, 56mL / hr, catalyst and 50%H 2 o 2 The mass ratio of the mixture is 1:8.5, the stirring speed is 350rpm, and the reaction temperature is 41-49°C. The reaction is an exothermic reaction, and the heat is exchanged through the jacket. The residence time is 1.5hr. The reaction material overflows from the upper end of the reactor and enters the filter device. After the water-phase catalyst slurry is separated by membrane filtration, the catalyst filter cake or concentrated slurry is directly beaten with a solvent, and then pumped into the epoxidation reaction kettle.

[0033] Reaction feeding ratio: n methanol: n chloropropene...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention provides a preparation method of chloroepoxy propane by chloropropene epoxidation. Chloropropene, a solvent and titanium silicalite molecular sieve catalyst fine particles are put in a reaction kettle for reaction at the temperature of 10-80 DEG C. The method is characterized in that the reaction kettle is a single kettle or multistage slurry bed reaction kettles with same or different volumes which are connected in series; the reaction solution needs not to be homogeneous phase, slurry particles of the chloropropene, the solvent and the titanium silicalite molecular sieve catalyst are added to a first stage reaction kettle by a metering pump, hydrogen peroxide is dropwise added to the first stage reaction kettle or each stage of the reaction kettles, the reaction occurs in a weakly acidic condition, materials are subject to oil-water delamination after the reaction to be divided into oil-phase slurry and water-phase slurry; the catalyst is suspended in the water phase, and the oil phase is sent to a rectification tower to separate the chloropropene, the epichlorohydrin and trace methanol; the water phase slurry is filtered, a catalyst filter cake or concentrated slurry is directly beaten by the solvent, and pumped to a first stage epoxidation reaction kettle, the water phase slurry contains the methanol, trace epichlorohydrin and the water which is generated by the reaction and the water which is taken by the hydrogen peroxide, the trace methanol and the epichlorohydrin are separated out by negative pressure rectification, and the recovered methanol is used for preparation of the catalyst slurry. The method has the advantages of simple process, little solvent consumption and high product separation yield, and is available for industrialized production.

Description

technical field [0001] The present invention relates to the production method of epichlorohydrin, specifically, relates to a kind of using titanium-silicon molecular sieve as catalyst, hydrogen peroxide as oxidant, carrying out slurry bed continuous reaction, catalyzing the direct epoxidation production of chloropropene The method for epichlorohydrin belongs to the technical field of organic chemical industry. Background technique [0002] Epichlorohydrin (ECH) is an important bulk organic chemical raw material and fine chemical product, and is the third largest epoxide in output after ethylene oxide and propylene oxide. Widely used in the synthesis of epoxy resin, glycerin, chlorohydrin rubber, etc. [0003] At present, epichlorohydrin is produced from propylene as a raw material, and the production method is mainly the chlorohydrin method, which is an indirect method for synthesizing epichlorohydrin from allyl chloride (AC), and the synthetic route is relatively long. Th...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(China)
IPC IPC(8): C07D303/08C07D301/12
Inventor 徐林吴惠丁克鸿顾志强于洋顾咸健戚明甫缪荣荣宋桂成陈林华王东生
Owner JIANGSU YANGNONG CHEM GROUP
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products