Method for reducing dioxin in preparation of chloranil

A technology of chloranil and chlorine gas, which is applied in the field of dioxin reduction in the preparation of chloranil, can solve the problems of low dioxin content, high production cost and waste water treatment cost, and can not be achieved, and achieves simple preparation process , High production efficiency, the effect of improving production efficiency

Active Publication Date: 2018-10-09
许克宇
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Since the late 1990s, my country has generally adopted the hydroquinone method instead of the phenol method to produce chloranil products. Although the content is lower than the phenol process, it can reach the chemical concentration of dioxin ≤ 100ppb, but it cannot reach the dioxin toxicity equivalent (higher index than the detection chemical concentration) of high-standard products ≤ 100ppt
There is the technology that adopts hydrochloric acid and the organic solvent (such as chlorobenzene, o-dichlorobenzene and p-dichlorobenzene etc.) mixed solution of hydrochloric acid and insoluble in hydrochloric acid to prepare tetrachlorobenzoquinone in the patent disclosed i

Method used

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  • Method for reducing dioxin in preparation of chloranil

Examples

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example 01

[0027] [Example 01] Mix 600g of glacial acetic acid, 200g of 35% hydrochloric acid, and 30g of ammonium chloride with a 1000ml glass reactor, heat up to 70°C and keep for 10 minutes to filter to obtain mother liquor M0.3-00; 45g of hydroquinone, 20g of p-aminophenol, and mother liquor M0.3-00 were stirred and mixed, and when the temperature was raised to 70°C, the chlorine flow (80g / hour) was passed, and after 3.5 hours, the chlorine flow was stopped, and the temperature was raised to 85°C for filtration: to obtain the mother liquor M0.3 -01 counts 710g and chloranil 141.5g of washing and drying.

example 02

[0028] [Example 02] Stir and mix the mother liquor M0.3-01+25% hydrochloric acid 90g, hydroquinone 50g, and p-aminophenol 15g, and introduce chlorine gas (80g / hour) when the temperature is raised to 80°C, stop the chlorine flow after 3.5 hours, Raise the temperature to 90° C. and filter: 680 g of mother liquor M0.3-02 and 141.2 g of chloranil were washed and dried.

example 03

[0029] [Example 03] Mix the mother liquor M0.3-02+120g of 15% hydrochloric acid, 60g of hydroquinone, and 5g of p-aminophenol, stir and mix and introduce chlorine gas (80g / hour) when the temperature is raised to 85°C, stop the chlorine flow for 3.5 hours, Raise the temperature to 95° C. and filter: 690 g of mother liquor M0.3-03 and 139.6 g of chloranil were washed and dried.

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Abstract

The invention relates to a method for reducing dioxin in preparation of chloranil. The preparation method of the chloranil comprises the steps of stirring a mixed raw material containing hydroquinoneand an appropriate amount of p-aminophenol for enabling the material to be dissolved in an acetic acid solution, wherein the mass ratio of acetic acid in the acetic acid solution is 20-80wt%, and themass ratio of the mixed raw material to the acetic acid solution is less than or equal to 15 wt%; then, introducing chlorine gas while stirring, carrying out a reaction at 50-90 DEG C, sampling in different periods, and stopping the introduction of the chlorine gas when the melting point of a target material is detected to be higher than or equal to 292 DEG C so as to obtain crystals of the chloranil and crystals of ammonia chloride; adding an appropriate amount of ammonium chloride during first kettle production, wherein the adding amount of the ammonium chloride and the controlling amount ofammonium chloride are the presence of ammonia chloride crystals in mother liquid at the chlorination reaction temperature; after a chlorination reaction is finished, heating up to 60-105 DEG C, wherein the temperature of the chlorination reaction is increased by 10-15 DEG C; filtering the chloranil material when the ammonium chloride salt crystals do not exist, and recovering the mother liquor obtained after filtration for the following use.

Description

1. Technical field [0001] The invention relates to a method for reducing dioxins in the preparation of compounds such as dyes, medicines, and agricultural intermediates, especially in the preparation of chloranil. 2. Background technology [0002] Chlorobenzoquinone, yellow powder, melting point 292°C, commonly used in industries such as pharmaceutical intermediates and permanent violet pigments, and some are exported. Chlorobenzoquinone chemical reaction formula and existing technological process are as follows: [0003] [0004] Raw material consumption: per ton of finished product of chlorobenzoquinone, 0.45 tons of hydroquinone and 1.44 tons of liquid chlorine are required; the mother liquor for chlorine flow is an aromatic hydrocarbon solution, and hydrogen chloride is recovered as hydrochloric acid at the same time. The target material must be washed with water before drying The liquid can be mixed into the mother liquor, and the subsequent water can be recycled. ...

Claims

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Application Information

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IPC IPC(8): C07C46/06C07C50/24
CPCC07C46/06C07C2601/16C07C50/24
Inventor 许克宇
Owner 许克宇
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