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Method for producing dichlorohydrin through glycerol chlorination

A technology of dichloropropanol and glycerin, which is applied in the direction of chemical instruments and methods, organic chemistry, catalyst carriers, etc., can solve the problems of poor selectivity and difficulty in catalyst recovery, achieve low energy consumption and cost, and be suitable for industrial production and use. Good catalytic stability

Active Publication Date: 2016-12-14
HUANGSHAN HUIZHOU TIANMA CHEM
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0010] For this reason, the technical problem to be solved by the present invention is to provide a method for producing dichloropropanol by chlorination of glycerol to solve the problems of poor selectivity and difficult catalyst recovery in the preparation reaction of dichloropropanol in the prior art

Method used

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  • Method for producing dichlorohydrin through glycerol chlorination
  • Method for producing dichlorohydrin through glycerol chlorination
  • Method for producing dichlorohydrin through glycerol chlorination

Examples

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Embodiment 1

[0026] The method for preparing dichloropropanol by chlorination of glycerol described in this example comprises the following steps: take 100 kg of glycerin and 0.2 kg of an active catalyst and mix them in a reactor, and control the temperature of the reaction system to 80° C., and then 60mL·min -1 The flow rate is passed into excess HCl gas to carry out the chlorination reaction for 5h, and after the tail gas is condensed, it is absorbed by NaOH solution to remove unreacted HCl. After the reaction is over, the product is filtered to recover the active catalyst. After washing, drying and activation, for recycling.

[0027] In the method of the present embodiment, described active catalyst uses Co 2 o 3 · MnO 2 · Fe 2 o 3 As the active component, with Zn(NO 3 ) 2 It is an active auxiliary agent, and it is prepared by dipping and coating on the surface of cordierite ceramic balls in the form of slurry. The specific preparation steps include:

[0028] (1) Take 390g cobal...

Embodiment 2

[0032] The method for preparing dichloropropanol by chlorination of glycerol described in this example comprises the following steps: take 100 kg of glycerin and 0.05 kg of an active catalyst and mix them in a reactor, and control the temperature of the reaction system to 70° C., then 50mL·min -1 The flow of excess HCl gas is passed through for chlorination reaction for 5-8h, and the tail gas is condensed and absorbed by NaOH solution to remove unreacted HCl. After the reaction, the product is filtered to recover the active catalyst, washed, dried and activated. After that, it is recycled.

[0033] In the method of the present embodiment, described active catalyst uses Co 2 o 3 · MnO 2 · Fe 2 o 3 As the active component, with Zn(NO 3 ) 2 It is an active auxiliary agent, and it is prepared by dipping and coating on the surface of activated alumina in the form of slurry. The specific preparation steps include:

[0034] (1) Take 78g cobalt nitrate hexahydrate (equivalent to...

Embodiment 3

[0038] The method for preparing dichloropropanol by chlorination of glycerol described in this example comprises the following steps: take 100 kg of glycerin and 0.1 kg of an active catalyst and mix them in a reactor, and control the temperature of the reaction system to 60° C., and then 80mL·min -1 The flow of excess HCl gas is passed through for chlorination reaction for 5-8h, and the tail gas is condensed and absorbed by NaOH solution to remove unreacted HCl. After the reaction, the product is filtered to recover the active catalyst, washed, dried and activated. After that, it is recycled.

[0039] In the method of the present embodiment, described active catalyst uses Co 2 o 3 · MnO 2 · Fe 2 o 3 As the active component, with Zn(NO 3 ) 2 It is an active auxiliary agent, and it is prepared by dipping and coating on the surface of cordierite honeycomb ceramics in the form of slurry. The specific preparation steps include:

[0040] (1) Take 39g cobalt nitrate hexahydra...

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Abstract

The invention belongs to the technical field of compound preparation, and particularly relates to a method for producing dichlorohydrin through glycerol chlorination. The method comprises the steps that a catalytic chlorination reaction is conducted by taking glycerol as a raw material and taking HCl as gas through an existing conventional technology, and an active catalyst is prepared by taking compounds of cobalt, compounds of manganese and compounds of iron as active components, taking compounds of zinc as active auxiliaries and applying the active components and the active auxiliaries to the surface of a catalyst carrier. According to the method, positive catalysis of a dichlorohydrin reaction can be effectively catalyzed, and obtained dichlorohydrin (including 1,3-dichlorohydrin and 1,2-dichlorohydrin) is good in selectivity and high in target product yield.

Description

technical field [0001] The technical field of compound preparation of the present invention, in particular relates to a method for producing dichloropropanol by chlorination of glycerol. Background technique [0002] Epichlorohydrin is an important organic chemical raw material and fine chemical product, and it is also the main raw material for the preparation of epoxy resin, with a wide range of uses. The epoxy resin prepared from epichlorohydrin has the advantages of strong adhesion, resistance to chemical medium corrosion, low shrinkage, good chemical stability, high impact strength and excellent dielectric properties. It is used in coatings, adhesives, etc. It has a wide range of applications in industries such as additives, reinforcement materials, casting materials and electronic laminates. my country's epoxy resin industry is in a golden period of development. It is the world's largest producer and consumer of epoxy resin, and has become the main driving force for th...

Claims

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Application Information

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IPC IPC(8): C07C29/62C07C31/36B01J23/06B01J23/34B01J23/745B01J23/75B01J32/00
CPCB01J23/06B01J23/34B01J23/745B01J23/75B01J32/00B01J37/0213B01J37/0234C07C29/62C07C31/36
Inventor 马万升程明光程鹏飞
Owner HUANGSHAN HUIZHOU TIANMA CHEM