Method for preparing halogen ethyl alcohol and ethylene oxide

A technology of ethylene oxide and haloethanol, which is applied in the preparation of haloethanol, the preparation of ethylene oxide by the new haloalcohol method, and the field of preparation of ethylene oxide, which can solve the problems of generating dichloroethane, serious corrosion, waste of raw materials, etc. problems, to achieve the effect of less steam consumption, lower biological oxygen content, and lighten the load

Active Publication Date: 2017-03-22
JIANGXI SUKEER NEW MATERIAL
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  • Abstract
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  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] The preparation of ethylene oxide by the chlorohydrin method of the prior art mainly has the following problems: 1. raw material chlorine and ethylene undergo an addition side reaction to generate ethylene dichloride
Dichloroethane is difficult to utilize and wastes a lot of raw materials
In addition, chlorine gas reacts with ethylene to release a large amount of heat, which is concentrated in the reaction vessel, resulting in great production hazards.
②A small amount of oxygen is inevitably entrained in the raw material chlorine gas during the production process. As the reaction proceeds, chlorine gas continuously participates in the reaction, so chlorine gas needs to be continuously replenished, while oxygen cannot participate in the reaction and accumulates in the reaction device continuously. , the oxygen con

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  • Method for preparing halogen ethyl alcohol and ethylene oxide
  • Method for preparing halogen ethyl alcohol and ethylene oxide
  • Method for preparing halogen ethyl alcohol and ethylene oxide

Examples

Experimental program
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Effect test

Embodiment 1

[0086] 1) Haloalcoholization: Add 70wt% concentration of hydrogen peroxide H 2 o 2 , HCl solution (hydrochloric acid) and ethene of 35wt% concentration, carry out chloroalcoholization reaction at the temperature of 45 ℃, wherein the hydrogen peroxide H of 70wt% concentration 2 o 2 , 35wt% concentration of HCl solution and ethylene flow should make H 2 The molar ratio of O to HCl to ethylene is about 1.2:1.2:1. This gives the halohydrin, a mixture of 2-chloroethan-1-ol and 1-chloroethan-2-ol.

Embodiment 2

[0090] 1) Haloalcoholization: add TS-1 molecular sieve, 35wt% concentration of hydrogen peroxide H in the tower reactor 2 o 2 , HCl solution (hydrochloric acid) and ethylene of 20wt% concentration, carry out chlorohydrinization reaction at the temperature of 35 ℃, wherein the molar ratio of TS-1 molecular sieve and ethylene is 0.05:1, the hydrogen peroxide H of 35wt% concentration 2 o 2 , 20wt% concentration of HCl solution and ethylene should be added in such a way that H 2 o 2 The mass ratio of HCl to ethylene is about 1.5:1.1:1. This gives the halohydrin, a mixture of 2-chloroethan-1-ol and 1-chloroethan-2-ol. Wherein, the synthesis method of TS-1 refers to Example 1 of CN201410812216.8.

Embodiment 3

[0098] 1) Haloalcoholization: Add 70wt% concentration of hydrogen peroxide H 2 o 2 , HCl solution (hydrochloric acid) and ethene of 35wt% concentration, carry out chloroalcoholization reaction at the temperature of 45 ℃, wherein the hydrogen peroxide H of 70wt% concentration 2 o 2 , 35wt% concentration of HCl solution and ethylene flow should make H 2 o 2 The molar ratio of HCl to ethylene is about 1.2:1.2:1. This gives the halohydrin, a mixture of 2-chloroethan-1-ol and 1-chloroethan-2-ol.

[0099] 2) Saponification: performing saponification reaction with the halohydrin obtained in step 1) and sodium hydroxide, and separating to obtain an ethylene oxide organic phase and a sodium chloride solution. The saponification reaction is carried out in a steel tower reactor, and the upper part is designed as a sieve tray tower. Steam enters from the bottom of the tower to blow out the crude ethylene oxide generated from the top of the tower. The saponification temperature is c...

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Abstract

The invention provides a method for preparing halogen ethyl alcohol. The method comprises the following step: (1) halogen alcoholization: adding halogen hydride, H2O2, ethylene and a Ti heteroatom-containing molecular sieve into a reaction device, and carrying out halogen alcoholization reaction to obtain the halogen ethyl alcohol. The invention also provides a method for preparing ethylene oxide with a halogenohydrin method. The method comprises the following steps: (1) halogen alcoholization: adding halogen hydride, H2O2, ethylene and a Ti heteroatom-containing molecular sieve into the reaction device, and carrying out the halogen alcoholization reaction to obtain the halogen ethyl alcohol; (2) saponification: carrying out saponification reaction on the halogen ethyl alcohol in the step (1) and a hydroxide of alkali metal, and separating to obtain the ethylene oxide and alkali halide metal salt; optionally (3) electroosmosis: carrying out bipolar membrane electroosmosis on alkali halide metal salt obtained in step (2) to obtain the hydroxide of alkali metal and the halogen hydride. According to the methods, the halogen ethyl alcohol or the ethylene oxide can be prepared at extremely high selectivity and yield, and the discharging of waste water and waste residues can be drastically lowered.

Description

technical field [0001] The invention relates to a preparation method of haloethanol, and a method for preparing ethylene oxide from haloethanol; more specifically, it provides a method for preparing haloethanol by using ethylene as a raw material and adopting a new haloalcohol method, and a method for preparing haloethanol by using a new haloalcohol method. Ethylene oxide method. Background technique [0002] 2-Chloroethanol (also called "chloroethane") is an important organic solvent and raw material for organic synthesis. It is used in the manufacture of ethylene oxide, synthetic rubber, dyes, medicines and pesticides, and is also used as an organic solvent. Used in the manufacture of ethylene glycol, ethylene oxide, and the synthesis of medicines, dyes, and pesticides. [0003] Ethylene oxide (hereinafter referred to as "EO") is an important organic chemical raw material. It is an organic compound with the chemical formula C2H4O, a toxic carcinogen that was previously ...

Claims

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Application Information

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IPC IPC(8): C07C31/36C07C29/64C07D301/26C07D303/04
Inventor 林民廖维林舒兴田
Owner JIANGXI SUKEER NEW MATERIAL
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