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The method for preparing ethylene glycol by hydrolysis of ethylene carbonate

A technology of ethylene carbonate and ethylene glycol, which is applied in the field of ethylene glycol hydrolysis of ethylene carbonate, can solve the problems of rapid decline in activity and easy swelling of resin catalysts, and achieve the effect of enhancing the resistance to temperature and swelling

Active Publication Date: 2017-08-11
CHINA PETROLEUM & CHEM CORP +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] The technical problem to be solved by the present invention is that there are problems in the prior art that the resin catalyst is easy to swell and the activity drops rapidly, and a new method for preparing ethylene glycol by hydrolysis of ethylene carbonate is provided

Method used

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  • The method for preparing ethylene glycol by hydrolysis of ethylene carbonate
  • The method for preparing ethylene glycol by hydrolysis of ethylene carbonate
  • The method for preparing ethylene glycol by hydrolysis of ethylene carbonate

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0033] Add 58.0 grams of styrene, 0.6 grams of divinylbenzene, 30 grams of polystyrene and 0.6 grams of benzoyl peroxide initiator in a 500 milliliter three-necked flask, and stir for 2.0 hours at 60°C; then add 2.8 grams of multi-walled carbon Nanotubes, continue stirring for 1 hour for pre-polymerization. 260 mL of deionized water in which 2.5 g of polyvinyl alcohol had been dissolved was added. Adjust the stirring speed, and at the same time gradually raise the temperature to 80°C, and react for 5 hours; then raise the temperature to 90°C, react for 5 hours, and finally raise the temperature to 98°C, and react for 6 hours. After the reaction, pour out the upper liquid, wash with 85°C hot water, then wash with cold water, then filter, put in an oven to dry at 80°C, sieve, and collect composite microspheres with a particle size within the range of 0.35 to 0.60 mm a.

[0034] Chloromethylation of composite microspheres: In a 500-ml three-necked flask, add 50 grams of composi...

Embodiment 2

[0038]In a 500 milliliter three-necked flask, add 20 grams of compound chlorine spheres A obtained in [Example 1], 150 milliliters of tetrahydrofuran, and 35.0 grams of tributylamine, stir and react under reflux for 30 hours, filter and remove the mother liquor after the reaction, and Wash with dichloromethane, acetone and water in sequence, and dry under vacuum to obtain chlorine-type nanocomposite quaternary ammonium salt resin A3.

[0039] The transformation of chlorine-type nanocomposite quaternary ammonium resin: in a 200 milliliter beaker, add 10 grams of chlorine-type nanocomposite quaternary ammonium resin A3, 20 grams of Ba(OH) 2 And 40 grams of deionized water, after stirring at room temperature for 18 hours, filter, wash with deionized water, repeat the above process 2 times, filter, wash with deionized water, dry under vacuum to obtain strong alkali type nano-composite quaternary ammonium salt Resin A4.

Embodiment 3

[0041] Add monomer mixture solution (60.0 gram styrene, 1.7 gram divinylbenzene, 60 gram polystyrene, 1.6 gram multi-walled carbon nanotube and 1.0 gram benzoyl peroxide containing initiator in 500 milliliters of three-necked flasks, The solution was first stirred and reacted at 70°C for 0.5 hours), started the agitator, added a mixed solution of 200 milliliters of deionized water and 5 grams of gelatin, raised the temperature to 85°C, reacted for 3 hours, then raised the temperature to 90°C, reacted for 9 hours, and finally The temperature was raised to 100° C., and the reaction was carried out for 10 hours. After the reaction, pour out the upper liquid, wash with 85°C hot water, then wash with cold water, then filter, put in an oven to dry at 80°C, sieve, and collect composite microspheres with a particle size within the range of 0.35 to 0.60 mm b.

[0042] Chloromethylation of composite microspheres: In a 500-ml three-necked flask, add 50 grams of composite microspheres B ...

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Abstract

The invention relates to a method for preparing ethylene glycol by hydrolyzing ethylene carbonate, which mainly solves the problems in the prior art that the resin is easy to swell and the activity decreases rapidly. The present invention adopts the conditions that ethylene carbonate and water are used as reaction raw materials, the reaction temperature is 60-180° C., the molar ratio of water and ethylene carbonate is 1-10, and the weight ratio of catalyst to ethylene carbonate is 0.005-1. Under this condition, the raw material is contacted with the catalyst for 1 to 8 hours to obtain ethylene glycol; wherein, the technical scheme that the catalyst is a strong base type nanocomposite quaternary ammonium salt resin solves this problem well, and can be used for the hydrolysis of ethylene carbonate to prepare ethylene glycol. In the industrial production of diols.

Description

technical field [0001] The invention relates to a method for preparing ethylene glycol by hydrolyzing ethylene carbonate. Background technique [0002] The hydrolysis of esters is an important chemical reaction, which is widely used in various fields of petrochemical production, among which the hydrolysis of cyclic carbonates, such as ethylene carbonate (EC), propylene carbonate, etc., has a very important basic position . [0003] The hydrolysis of EC is an important step in the production of ethylene glycol (EG) by the two-step catalytic hydration of ethylene oxide (EO). EG is an important organic chemical raw material, mainly used to produce polyester fiber, antifreeze, unsaturated polyester resin, nonionic surfactant, ethanolamine and explosives. The production technology of EG is mainly divided into petrochemical route and non-petrochemical route. In the petrochemical route, there are EO direct hydration method and EO catalytic hydration method. The direct hydration ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C07C31/20C07C29/12B01J31/08
CPCY02P20/52
Inventor 陈梁锋何文军
Owner CHINA PETROLEUM & CHEM CORP