CN1006546B - Treatment method of acid residuum - Google Patents

Treatment method of acid residuum

Info

Publication number
CN1006546B
CN1006546B CN 85102005 CN85102005A CN1006546B CN 1006546 B CN1006546 B CN 1006546B CN 85102005 CN85102005 CN 85102005 CN 85102005 A CN85102005 A CN 85102005A CN 1006546 B CN1006546 B CN 1006546B
Authority
CN
China
Prior art keywords
acid
treatment method
oil
residuum
heated
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
CN 85102005
Other languages
Chinese (zh)
Other versions
CN85102005A (en
Inventor
盛芝芳
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Capital Iron & Steel Co
Original Assignee
Capital Iron & Steel Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Capital Iron & Steel Co filed Critical Capital Iron & Steel Co
Priority to CN 85102005 priority Critical patent/CN1006546B/en
Publication of CN85102005A publication Critical patent/CN85102005A/en
Publication of CN1006546B publication Critical patent/CN1006546B/en
Expired legal-status Critical Current

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  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
  • Removal Of Specific Substances (AREA)
  • Solid Fuels And Fuel-Associated Substances (AREA)

Abstract

Acid residuum formed in the process of chemical purification is heated to flow, and then, is additionally provided with ammonia water of certain consistence; a certain temperature is kept; oil and ammonium sulfate solution, which are formed by reaction, are naturally layered and can be separately poured into a storage tank.

Description

Treatment method of acid residuum
The present invention is the treatment method of acid residuum in the chemical industry highly industry.
Acid sludge in Japan's J49-126701 patent is handled and is: in addition an amount of waste oil or light oil in the acid sludge, most of H 2SO 4Water-soluble, in the oil a spot of residual sulfuric acid with in the lime and after, can make heavy oil or be light oil through catalysis.This method neutralizes with lime, must have precipitation to become waste residue.
Acid sludge in the Japan J76-002919 patent is handled, with the H in the acid sludge 2SO 4Concentration adjust best 65-90%, be heated to 150-190 ℃ while stirring, make organism dehydrogenation and carbonization, filtration can get carbonized polymers and sulphuric acid soln, carbonized polymers can be used as activated carbon adsorbent, and this method also will add sulfuric acid when handling acid sludge, has sour gas to overflow with water vapor to cause environmental pollution being heated to 150-190 ℃, last sulphuric acid soln corrosion is also comparatively serious, the requirement for anticorrosion height.
Japan J53-144875 handles sulfur acid waste residue method: add Mg(OH) 2Slurries, refuel burns, and absorbs the SO that burning produces with aqueous suspension 2The MgSO that generates 4The aqueous solution be disposed to rivers, fuel that this method consumption is a large amount of and Mg(OH) 2, do not produce useful matter, and also generate MgSO at last 4The discharging rivers, still unfavorable in environmental protection.
Purpose of the present invention is exactly the problem that will solve above existence, makes the acid sludge after the processing all become available material.
Solution of the present invention:
But acid sludge is heated to flow state, after stopping heating, add ammoniacal liquor, the limit edged stirs, stop adding ammoniacal liquor during to PH=7, reaction is violent and rapid, is static layering after the reaction, and the division is clearly demarcated, the upper strata is an oil, lower floor is the sulphur aqueous ammonium, and the lower pipeline of reacting in the actual production should add transparent sight glass, and oil and ammonium sulfate solution are put into separately storage tank respectively.
The present invention compares with above-mentioned several method, does not produce MgSO 4Aqueous solution discharge does not need refuel to burn.
Do not produce lime and so on precipitation, decompose the oil that comes out to use at once, without catalytic decomposition.
Not existing to re-use sulfuric acid concentration adjusting problem, without filtration process, do not have throw out, is simple oil water separation process.
The novel substance that present method produces all is an available, does not waste material and does not also produce new pollutent.

Claims (1)

1, treatment method of acid residuum is characterized in that, but gluey acid sludge is heated to flow state, handles with ammoniacal liquor.
CN 85102005 1985-04-03 1985-04-03 Treatment method of acid residuum Expired CN1006546B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 85102005 CN1006546B (en) 1985-04-03 1985-04-03 Treatment method of acid residuum

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 85102005 CN1006546B (en) 1985-04-03 1985-04-03 Treatment method of acid residuum

Publications (2)

Publication Number Publication Date
CN85102005A CN85102005A (en) 1986-10-01
CN1006546B true CN1006546B (en) 1990-01-24

Family

ID=4792197

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 85102005 Expired CN1006546B (en) 1985-04-03 1985-04-03 Treatment method of acid residuum

Country Status (1)

Country Link
CN (1) CN1006546B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2045491B1 (en) * 2007-10-02 2020-12-02 Culligan International Company Control valve for a fluid treatment system

Also Published As

Publication number Publication date
CN85102005A (en) 1986-10-01

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