CN103664573A - Method for preparing sodium acetate from acetic acid waste gas through alkaline absorption - Google Patents

Method for preparing sodium acetate from acetic acid waste gas through alkaline absorption Download PDF

Info

Publication number
CN103664573A
CN103664573A CN201210355758.8A CN201210355758A CN103664573A CN 103664573 A CN103664573 A CN 103664573A CN 201210355758 A CN201210355758 A CN 201210355758A CN 103664573 A CN103664573 A CN 103664573A
Authority
CN
China
Prior art keywords
acetic acid
waste gas
alkali
acid waste
sodium acetate
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.)
Granted
Application number
CN201210355758.8A
Other languages
Chinese (zh)
Other versions
CN103664573B (en
Inventor
郭良臣
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.)
HUBEI YITAI PHARMACY Co.,Ltd.
Original Assignee
Hubei Yitai Pharmaceutical Co Ltd
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 Hubei Yitai Pharmaceutical Co Ltd filed Critical Hubei Yitai Pharmaceutical Co Ltd
Priority to CN201210355758.8A priority Critical patent/CN103664573B/en
Publication of CN103664573A publication Critical patent/CN103664573A/en
Application granted granted Critical
Publication of CN103664573B publication Critical patent/CN103664573B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/41Preparation of salts of carboxylic acids
    • C07C51/412Preparation of salts of carboxylic acids by conversion of the acids, their salts, esters or anhydrides with the same carboxylic acid part
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/46Removing components of defined structure
    • B01D53/72Organic compounds not provided for in groups B01D53/48 - B01D53/70, e.g. hydrocarbons
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/74General processes for purification of waste gases; Apparatus or devices specially adapted therefor
    • B01D53/77Liquid phase processes
    • B01D53/78Liquid phase processes with gas-liquid contact
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/10Process efficiency

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Environmental & Geological Engineering (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Biomedical Technology (AREA)
  • Analytical Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The invention relates to a method for preparing sodium acetate from acetic acid waste gas through alkaline absorption. The method comprises the following steps: 1, inputting acetic acid waste gas to an alkaline absorption tower through an induced draft fan to carry out multistage circulated alkaline absorption, and emptying the absorbed air, wherein the acetic acid waste gas is generated in a chemical industry or drug production process; 2, controlling the alkaline absorption liquid temperature between 30 DEG C and 80 DEG C, and adding solid sodium hydroxide or sodium carbonate when the pH value is less than or equal to 10; 3, stopping adding alkaline when the concentration of the added sodium hydroxide or sodium carbonate is up to 25-50%, and inputting alkaline absorption liquid to a crystallization kettle when the pH value of the alkaline absorption liquid is up to 8-9; 4, cooling the alkaline absorption liquid to 10 DEG C below zero to 30 DEG C, and carrying out centrifugal swing filtration to obtain sodium acetate trihydrate, or drying at the temperature of 120-150 DEG C to prepare anhydrous sodium acetate; and 5, adding centrifuged mother liquid into the alkaline absorption tower to be recycled, adding a hydrogen dioxide solution or potassium permanganate solution to decolor after the mother liquid turns yellow, wherein the mother liquid can be recycled. No new waste water, waste gas and waste residue are generated, and the production process is clean, environment-friendly, energy-saving and efficient.

Description

Acetic acid waste gas alkali absorbs the method for preparing sodium acetate
Technical field
 
Field of waste treatment in the present invention relates to that medicine is synthetic and producing, is specifically related to the processing method that acetic acid waste gas recovery and treatment method and acetic acid waste gas in Glucuronic acid .gamma.-lactone production process are prepared sodium acetate.
 
Background technology
?
In Glucuronic acid .gamma.-lactone production process, esterification is used acetic acid, when centrifugal drying material, produce a large amount of acetic acid gas, acetic acid gas has intense stimulus smell, affect production environment and atmospheric environment, take simple water spray-absorption in producing early stage, absorbs not exclusively, and part acetic acid gas still enters atmosphere, operating environment of pollution and atmospheric environment, must thoroughly administer.
Waste gas pollution control and treatment must have certain input, consumes new material, likely produces new pollution simultaneously.With acetic acid waste gas alkali absorption preparation sodium acetate trihydrate and anhydrous sodium acetate, be broad-spectrum product, it has good shock-absorbing capacity, applies to electroplate and dyeing; There is antiseptic property, as the sanitas of food and feed; As water purifying assistant and stopping agent; In chemosynthesis, use wider.It is a kind of fine chemical product being of wide application.
 
Summary of the invention
?
The object of the invention is the defect of processing for acetic acid waste gas absorption in Glucuronic acid .gamma.-lactone production process, improve acetic acid waste gas absorption treatment process, utilize acetic acid waste gas to prepare sodium acetate for raw material production, solve acetic acid exhaust emission problem and provide a kind of acetic acid waste gas alkali that utilizes to absorb the method for preparing sodium acetate
The technical scheme that realizes the object of the invention is:
Provide a kind of acetic acid waste gas alkali to absorb the method for preparing sodium acetate, it is characterized in that: it consists of following steps:
1, the acetic acid waste gas that in chemical industry or pharmaceutical production, (as Glucuronic acid .gamma.-lactone is produced in centrifugal drying material process) produces is inputted to alkali absorption tower by producing induced draft fan, as the raw material of producing sodium acetate, carry out multistage alkali circulation and absorb, the gas after absorption is emptying;
2, control alkali absorption liquid temperature between 30 to 80 ℃, use at any time pH detection paper alkali absorption liquid pH value, when pH value≤10, add solid state hydrogen sodium oxide or sodium carbonate;
When 3, cumulative calculation adds the concentration of sodium hydroxide or sodium carbonate to reach 25% to 50%, stop adding alkali, in the time of between alkali absorption liquid pH value reaches 8 to 9, by alkali absorption liquid input crystallization kettle;
4, alkali absorption liquid is cooled to-10 to 30 ℃, centrifugal rejection filter, obtains sodium acetate trihydrate, and sodium acetate trihydrate can direct marketing, also can be through 120 to 150 ℃ of dry anhydrous sodium acetates of preparing;
5, centrifuge mother liquor adds recycle in alkali absorption tower, adds superoxol or potassium permanganate solution decolouring after mother liquor its colour changed into yellow, guarantees that applying mechanically mother liquor does not affect quality product.
Acetic acid waste gas described in step 1, comprises the acetic acid waste gas producing in Glucuronic acid .gamma.-lactone production process, but is not limited to the acetic acid waste gas that produces in Glucuronic acid .gamma.-lactone production process.
Described in step 1, carry out multistage alkali absorption, comprise 1-5 level alkali absorption process.
Acetic acid waste gas alkali as above absorbs the method for preparing sodium acetate, it is characterized in that absorbing the alkali that acetic acid waste gas uses and includes but not limited to sodium hydroxide or sodium carbonate.
Control alkali absorption liquid temperature described in step 2, between 30---80 ℃, be take and is controlled at 50-65 ℃ as optimum.
Obviously, those skilled in the art also can make absorption agent by potassium hydroxide, ammoniacal liquor etc. and prepare potassium acetate, ammonium acetate by absorbing acetic acid waste gas, and the displacement of suchlike absorption agent and the acetate moiety salt that obtains do not depart from the present invention's essence place.
In the present invention, acetic acid waste gas is taked the mode that the circulation of multi-stage column alkali absorbs, and acetic acid off gas treatment is thorough; With acetic acid waste gas, substitute the raw material production sodium acetate costs such as acetic acid low; Utilize the mode that relatively-high temperature circulation alkali absorbs, gradation plus-minus improves acetic acid sodium reaction generation concentration, removed the technological process of concentrated raising sodium acetate concentration from, direct crystallization obtains sodium acetate, simplified technological process, reduce acetic acid waste gas alkali and absorbed steam consumption and the power consumption of producing in sodium acetate process, further reduced production cost; Mother liquor recirculation is applied mechanically, and does not have new waste waste water,waste gas and industrial residue to produce, be clean, the method for environmental protection, energy-conservation, High-efficient Production sodium acetate.
 
Accompanying drawing explanation
 
Fig. 1 is that the present invention's acetic acid waste gas alkali in Glucuronic acid .gamma.-lactone is produced absorbs the process flow diagram that preparation sodium acetate trihydrate is used.
?
Embodiment
 
Below in conjunction with accompanying drawing explanation embodiments of the invention, but be not limited to following examples:
Utilize acetic acid waste gas alkali to absorb preparation sodium acetate trihydrate and prepare example:
Technological process by Fig. 1 operates, in one-level alkali absorption tower He in secondary alkali absorption tower, add respectively 1000 liters, water, 96% 200 kilograms, sodium hydroxide, be heated to dissolve between 55-60 ℃, pump is beaten circulation absorption Glucuronic acid .gamma.-lactone workshop and is slightly got rid of the acetic acid waste gas that conveying is come, control alkali absorption temperature between 50-60 ℃, with pH test paper, measure pH in one-level alkali absorption tower at any time, when pH value approaches 10, add 96% sodium hydroxide, in one-level alkali absorption tower, add 96% sodium hydroxide total amount accumulative total and reach 400 kilograms, when liquid pH value to be absorbed reaches 8-9, absorption liquid is inputted to crystallization kettle, control-5 ℃ of crystallizations, rejection filter obtains sodium acetate trihydrate.Crystallization filtrate cover is for two-level absorption tower.
In one-level alkali absorption tower, after absorption liquid input crystallization kettle, absorption liquid in secondary alkali absorption tower is proceeded to one-level alkali absorption tower.Crystallization filtrate adds water and absorbs and join alkali solvent as secondary alkali, joins alkali at every turn and adds 200 kilograms, 96% sodium hydroxide and 15 liters of hydrogen peroxide.Carry out as stated above operate continuously successively, circulation absorbs continuous production sodium acetate trihydrate;
The technical data of continuous 5 batches of production sodium acetate trihydrate below:
Experiment lot number Sodium hydroxide concentration Hydrogen peroxide consumption Sodium acetate trihydrate output Remarks
01 400kg 0 1170kg Do not overlap mother liquor
02 400kg 0 1197 kg Do not overlap mother liquor
03 400kg 15L 1301 kg Apply mechanically mother liquor
04 400kg 15L 1295 kg Apply mechanically mother liquor
05 400kg 15L 1292 kg Apply mechanically mother liquor
Shown detailed embodiment of the present invention above, apparent, those skilled in the art, under prerequisite of the present invention, can carry out part modifications and changes; The content of mentioning in description above and accompanying drawing, only as illustrative case, is not limitation of the present invention; The acetic acid waste gas alkali with technical characterictic described herein absorbs the method for preparing sodium acetate, all falls into this patent protection domain.

Claims (5)

1. acetic acid waste gas alkali absorbs a method of preparing sodium acetate, it is characterized in that: it consists of following steps:
1, the acetic acid waste gas producing in chemical industry or pharmaceutical production is inputted to alkali absorption tower by induced draft fan, as the raw material of producing sodium acetate, carry out multistage alkali circulation and absorb, the gas after absorption is emptying;
2, control alkali absorption liquid temperature between 30 to 80 ℃, when pH value≤10, add solid state hydrogen sodium oxide or sodium carbonate;
When 3, cumulative calculation adds the concentration of sodium hydroxide or sodium carbonate to reach 25% to 50%, stop adding alkali, when alkali absorption liquid pH value reaches between 8-to 9, by alkali absorption liquid input crystallization kettle;
4, alkali absorption liquid is cooled to-10 to 30 ℃, centrifugal rejection filter, obtains sodium acetate trihydrate, and sodium acetate trihydrate can direct marketing, also can be through 120 to 150 ℃ of dry anhydrous sodium acetates of preparing;
5, centrifuge mother liquor adds recycle in alkali absorption tower, adds superoxol or potassium permanganate solution decolouring after mother liquor its colour changed into yellow.
2. acetic acid waste gas alkali as claimed in claim 1 absorbs the method for preparing sodium acetate, it is characterized in that: the acetic acid waste gas described in step 1, comprise the acetic acid waste gas producing in Glucuronic acid .gamma.-lactone production process, but be not limited to the acetic acid waste gas that produces in Glucuronic acid .gamma.-lactone production process.
3. acetic acid waste gas alkali as claimed in claim 1 absorbs the method for preparing sodium acetate, it is characterized in that: described in step 1, carry out multistage alkali absorption, comprise 1-5 level alkali absorption process.
4. acetic acid waste gas alkali as claimed in claim 1 absorbs the method for preparing sodium acetate, it is characterized in that: the alkali that described absorption acetic acid waste gas is used includes but not limited to sodium hydroxide or sodium carbonate.
5. acetic acid waste gas alkali as claimed in claim 1 absorbs the method for preparing sodium acetate, it is characterized in that: the control alkali absorption liquid temperature described in step 2, between 30---80 ℃, be take and is controlled at 50-65 ℃ as optimum.
CN201210355758.8A 2012-09-24 2012-09-24 Acetic acid waste gas Alkali absorption prepares the method for sodium acetate Active CN103664573B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201210355758.8A CN103664573B (en) 2012-09-24 2012-09-24 Acetic acid waste gas Alkali absorption prepares the method for sodium acetate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201210355758.8A CN103664573B (en) 2012-09-24 2012-09-24 Acetic acid waste gas Alkali absorption prepares the method for sodium acetate

Publications (2)

Publication Number Publication Date
CN103664573A true CN103664573A (en) 2014-03-26
CN103664573B CN103664573B (en) 2016-06-01

Family

ID=50303469

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201210355758.8A Active CN103664573B (en) 2012-09-24 2012-09-24 Acetic acid waste gas Alkali absorption prepares the method for sodium acetate

Country Status (1)

Country Link
CN (1) CN103664573B (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016110081A1 (en) * 2015-01-09 2016-07-14 南京格洛特环境工程股份有限公司 Acid waste gas treatment and resource utilization
CN105948151A (en) * 2016-05-12 2016-09-21 神华集团有限责任公司 System and method for treating Fischer-Tropsch synthesis wastewater
CN106800506A (en) * 2016-12-30 2017-06-06 杭州垚信生物科技有限公司 A kind of preparation method of anhydrous sodium acetate
CN108892611A (en) * 2018-06-27 2018-11-27 蓝保(厦门)水处理科技有限公司 A kind of production technology of sodium acetate solution
CN111423322A (en) * 2020-05-12 2020-07-17 无锡阳山生化有限责任公司 Sodium acetate preparation method and energy-saving preparation system thereof
CN112300166A (en) * 2020-10-06 2021-02-02 湖北益泰药业股份有限公司 Method for separating acyclovir and sodium acetate from mother liquor

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0603548A1 (en) * 1992-12-17 1994-06-29 Hoechst Aktiengesellschaft Acetate of sodium and alkaline earth metal, process of preparation and use
CN101429111A (en) * 2008-12-17 2009-05-13 安徽富博医药化工股份有限公司 Comprehensive processing method and apparatus for mother solution in production of glucurolactone
CN101898953A (en) * 2009-05-27 2010-12-01 薛平 Technological research for producing sodium acetate by comprehensively utilizing chemical waste liquid
CN102372619A (en) * 2010-08-23 2012-03-14 刘同清 Process for producing acetate by using dilute acetic acid

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0603548A1 (en) * 1992-12-17 1994-06-29 Hoechst Aktiengesellschaft Acetate of sodium and alkaline earth metal, process of preparation and use
CN101429111A (en) * 2008-12-17 2009-05-13 安徽富博医药化工股份有限公司 Comprehensive processing method and apparatus for mother solution in production of glucurolactone
CN101898953A (en) * 2009-05-27 2010-12-01 薛平 Technological research for producing sodium acetate by comprehensively utilizing chemical waste liquid
CN102372619A (en) * 2010-08-23 2012-03-14 刘同清 Process for producing acetate by using dilute acetic acid

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016110081A1 (en) * 2015-01-09 2016-07-14 南京格洛特环境工程股份有限公司 Acid waste gas treatment and resource utilization
CN105948151A (en) * 2016-05-12 2016-09-21 神华集团有限责任公司 System and method for treating Fischer-Tropsch synthesis wastewater
CN106800506A (en) * 2016-12-30 2017-06-06 杭州垚信生物科技有限公司 A kind of preparation method of anhydrous sodium acetate
CN108892611A (en) * 2018-06-27 2018-11-27 蓝保(厦门)水处理科技有限公司 A kind of production technology of sodium acetate solution
CN111423322A (en) * 2020-05-12 2020-07-17 无锡阳山生化有限责任公司 Sodium acetate preparation method and energy-saving preparation system thereof
CN112300166A (en) * 2020-10-06 2021-02-02 湖北益泰药业股份有限公司 Method for separating acyclovir and sodium acetate from mother liquor

Also Published As

Publication number Publication date
CN103664573B (en) 2016-06-01

Similar Documents

Publication Publication Date Title
CN103664573A (en) Method for preparing sodium acetate from acetic acid waste gas through alkaline absorption
CN108484796B (en) Preparation process of low-molecular sodium hyaluronate
CN106185995A (en) Sodium bromide preparation method
CN101671374A (en) New technique for extracting D-glucosamine hydrochloride
CN102010318A (en) Method for producing mixed long carbon chain dibasic acid
CN203079884U (en) Series-connection discoloring device for potassium sorbate
CN106495174A (en) Attapulgite wet method bisgallic acid activation method
CN112815638A (en) Method for drying erythromycin thiocyanate fungus residues
CN104211657A (en) Refining method of rubber vulcanizing accelerant M
CN103613685A (en) Method for preparing chitin through subcritical hydrolysis of arthropod shells
CN104261468B (en) A kind of manufacture method of low alkali catalysis titanium white
CN105001287B (en) The preparation method of AVM
CN109627355A (en) A kind of method that ionic liquid degradation chitosan prepares Water soluble oligo chitosan
CN204097371U (en) The production equipment of potassium sorbate
Yan et al. Microwave-assisted depolymerization of chitin and chitosan extracted from crayfish shells waste: A sustainable approach based on graphene oxide catalysis
CN204917971U (en) Sour concentrated decoloration equipment of organic sulfur waste
CN104587810B (en) A kind of method of comprehensive utilization of the chlorination tail gas of itrated compound
CN113372572A (en) Method for separating lignin by recycling solid organic acid
CN203639166U (en) Three-section incinerator-based comprehensive industrial waste salt treatment device
CN206288970U (en) A kind of thio conversion ammonium sulfate process equipment of desulphurization waste liquid of coke oven gas salt extraction
CN105506033A (en) Preparation method of low-gel-strength agar
CN105381700B (en) The oxidized tail gas processing system and method for the raw materials used aminobenzoic acid of EHA, EDB
CN104193836A (en) Production process for medicinal hydroxypropyl starch
CN107417512A (en) A kind of method of one-step synthesis sodium acetate
CN108772096A (en) The advanced oxidation processes of lavo-ofloxacin hydrochloride are handled in a kind of heterogeneous reaction system

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
CP03 Change of name, title or address
CP03 Change of name, title or address

Address after: 431700 fengchengyuan, Tianmen suburb, Jingzhou City, Hubei Province

Patentee after: HUBEI YITAI PHARMACY Co.,Ltd.

Address before: 431700 Hubei provincial administrative units under Fengcheng embankment on the outskirts of Tianmen

Patentee before: HUBEI YITAI PHARMACEUTICAL Co.,Ltd.