CN102502508A - Method for preventing invalid reaction in process of preparing chlorine dioxide with sodium chlorate reduction method - Google Patents

Method for preventing invalid reaction in process of preparing chlorine dioxide with sodium chlorate reduction method Download PDF

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Publication number
CN102502508A
CN102502508A CN2011103452295A CN201110345229A CN102502508A CN 102502508 A CN102502508 A CN 102502508A CN 2011103452295 A CN2011103452295 A CN 2011103452295A CN 201110345229 A CN201110345229 A CN 201110345229A CN 102502508 A CN102502508 A CN 102502508A
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China
Prior art keywords
reaction
acidity
reduction method
chlorine dioxide
sodium chlorate
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CN2011103452295A
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Inventor
穆超银
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Chengdu Jinxing Lvyuan Environmental Protection Technology Co Ltd
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Chengdu Jinxing Lvyuan Environmental Protection Technology Co Ltd
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Priority to CN2011103452295A priority Critical patent/CN102502508A/en
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Abstract

The invention discloses a method for preventing an invalid reaction in a process of preparing chlorine dioxide with a sodium chlorate reduction method. The method comprises the following steps of: before the reaction, adding methanol until adjusting the acidity to at least be up to 3.5 mol/L and simultaneously maintaining the acidity of a reaction solution to be not lower than 3.5 mo/L until the reaction is finished; and meanwhile, controlling the acidity to be not more than 7 mol/L before a solid is formed, so as to avoid the invalid reaction. When the solid appears, the acidity can be improved to a normal value of 8.0-8.2 mol/L. According to the invention, by controlling the acidity of the reaction through using sulfuric acid, the invalid reaction can be better prevented and the reaction efficiency can be improved.

Description

Prevent the method for abortive response when the VAL-DROP reduction method prepares dioxide peroxide
Technical field
The present invention relates to a kind of method that prevents invalid chemical reaction, be specifically related to a kind of VAL-DROP reduction method that prevents and prepare the method for dioxide peroxide system abortive response.
Background technology
The VAL-DROP reduction method prepares dioxide peroxide, and mainly to use pure VAL-DROP, methyl alcohol and sulphuric acid soln be raw material; Under acidic conditions, make reductive agent generation dioxide peroxide with methyl alcohol; Refrigerated water absorption through with 7 ℃ makes Chlorine Dioxide Steady Liquor, and the flow of regulating refrigerated water is to obtain the ClO of desired concn (8-10g/L) 2Solution.System's tail gas send washs the ClO that washes in the tower washing and recycling tail gas 2After enter atmosphere.This method principal reaction formula: 6NaClO 3+ 4H 2SO 4+ CH 3OH → 6ClO 2+ 5H 2O+2Na 3H (SO 4) 2+ CO 2↑.
The characteristics of present method are that technical process is simple, throughput and reaction efficiency is high, raw material consumption is low, technical maturity, processing ease, change of production flexibility are big, be easy to regulate, ClO 2Purity is high, contains chlorine hardly.Adopt reduction method to prepare ClO 2The sub product saltcake that is produced can use in inside plants, reaches the equilibrium of supply and demand basically, compares the discharging that has reduced pollutent with other method.
But when utilizing the VAL-DROP reduction method to prepare dioxide peroxide,, then possibly cause to produce ClO if the additional proportion of several kinds of material compositions is improper 2Product.As because acidity is too high, can cause the generation of abortive response.
Summary of the invention
The object of the present invention is to provide a kind of method of abortive response when preventing that the VAL-DROP reduction method from preparing dioxide peroxide.
The present invention is achieved in that
Prevent the method for abortive response when the VAL-DROP reduction method prepares dioxide peroxide; Be before reaction; Regulate acidity
Figure BDA0000105630420000021
and begin to add methyl alcohol when reaching 3.5mol/L at least; To keep adding the vitriolic flow simultaneously; The acidity
Figure BDA0000105630420000022
of keeping reaction solution is not less than 3.5mol/L and stops until reaction; Simultaneously before solid forms; Want controlling acidity
Figure BDA0000105630420000023
to be not more than 7mol/L; To avoid occurring abortive response, after solid occurs, just can improve acidity
Figure BDA0000105630420000024
and reach normal 8.0~8.2mol/L.
The present invention carries out acidity control through using sulfuric acid to reaction, can prevent the generation of abortive response well, and can improve reaction efficiency.
Embodiment
Prevent the method for abortive response when the VAL-DROP reduction method prepares dioxide peroxide; Be before reaction; Regulate acidity
Figure BDA0000105630420000025
and begin to add methyl alcohol when reaching 3.5mol/L at least; To keep adding the vitriolic flow simultaneously; The acidity
Figure BDA0000105630420000026
of keeping reaction solution is not less than 3.5mol/L and stops until reaction; Simultaneously before solid forms; Want controlling acidity
Figure BDA0000105630420000027
to be not more than 7mol/L; To avoid occurring abortive response, after solid occurs, just can improve acidity
Figure BDA0000105630420000028
and reach normal 8.0~8.2mol/L.

Claims (1)

1. the method for an abortive response when preventing that the VAL-DROP reduction method from preparing dioxide peroxide; It is characterized in that: before reaction; Regulate acidity
Figure FDA0000105630410000011
and begin to add methyl alcohol when reaching 3.5mol/L at least; Keep adding the vitriolic flow simultaneously; The acidity
Figure FDA0000105630410000012
of keeping reaction solution is not less than 3.5mol/L and stops until reaction; Before solid forms; Controlling acidity
Figure FDA0000105630410000013
is not more than 7mol/L simultaneously, back raising acidity
Figure FDA0000105630410000014
occurs as solid and reaches normal 8.0~8.2mol/L.
CN2011103452295A 2011-11-04 2011-11-04 Method for preventing invalid reaction in process of preparing chlorine dioxide with sodium chlorate reduction method Pending CN102502508A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2011103452295A CN102502508A (en) 2011-11-04 2011-11-04 Method for preventing invalid reaction in process of preparing chlorine dioxide with sodium chlorate reduction method

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Application Number Priority Date Filing Date Title
CN2011103452295A CN102502508A (en) 2011-11-04 2011-11-04 Method for preventing invalid reaction in process of preparing chlorine dioxide with sodium chlorate reduction method

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CN102502508A true CN102502508A (en) 2012-06-20

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CN (1) CN102502508A (en)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1067224A (en) * 1991-04-22 1992-12-23 田纳科加拿大分公司 The metathesis of the acidic by-products of chlorine dioxide production technology

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1067224A (en) * 1991-04-22 1992-12-23 田纳科加拿大分公司 The metathesis of the acidic by-products of chlorine dioxide production technology

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Application publication date: 20120620