CN1327934C - Method for absorbing SO2 gas by alcoholamine carboxylate ion liquid - Google Patents

Method for absorbing SO2 gas by alcoholamine carboxylate ion liquid Download PDF

Info

Publication number
CN1327934C
CN1327934C CNB2005100694066A CN200510069406A CN1327934C CN 1327934 C CN1327934 C CN 1327934C CN B2005100694066 A CNB2005100694066 A CN B2005100694066A CN 200510069406 A CN200510069406 A CN 200510069406A CN 1327934 C CN1327934 C CN 1327934C
Authority
CN
China
Prior art keywords
liquid
gas
ion liquid
absorption bottle
ionic liquid
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 - Fee Related
Application number
CNB2005100694066A
Other languages
Chinese (zh)
Other versions
CN1698928A (en
Inventor
张锁江
袁晓亮
陈玉焕
张延强
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.)
Beijing Zhongke Neiyin AI Technology Co. Ltd.
Original Assignee
Institute of Process Engineering of CAS
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 Institute of Process Engineering of CAS filed Critical Institute of Process Engineering of CAS
Priority to CNB2005100694066A priority Critical patent/CN1327934C/en
Publication of CN1698928A publication Critical patent/CN1698928A/en
Application granted granted Critical
Publication of CN1327934C publication Critical patent/CN1327934C/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The present invention relates to a method for absorbing SO2 by alcohol amine carboxylate ionic liquid in the chemical field. Etha nolam ine, diethanolamine, triethanolmine, diglycolamine, and the like are neutralized with acetic acid, lactic acid or acid with the similar structure respectively at normal temperature to generate a series of corresponding basic ionic liquid, and the ionic liquid is used for absorbing SO2 (a kind of acidic gas) under the conditions of normal temperature and pressure in a mode of pure liquid or in a mode that the liquid is loaded on the carrier. The present invention has the advantages of high absorption efficiency, short equilibration time, etc.

Description

Absorb SO with alcoholamine carboxylate ion liquid 2The method of gas
Technical field:
The present invention relates to absorb SO with a kind of with alcoholamine carboxylate ion liquid in the chemical field 2The application of gas.
Background technology:
Ionic liquid is by organic cation and inorganic or organic anion constitutes, be the salt of liquid condition under near temperature normal temperature or the normal temperature.Ionic liquid is as a kind of emerging solvent and reaction medium, because unique physicochemical properties such as it is non-volatile, structure can design, having a extensive future of fields such as extract and separate, catalytic reaction, be expected to replace volatile environmentally harmful conventional organic solvents in 21 century.
In recent years because deleterious acidic gas (SO 2, NO xAnd CO 2) pollution is serious day by day, and the limitation of existing treatment technology, a lot of people consider with ionic liquid as the solvent that absorbs sour gas.But a lot of ionic liquids of existing research are all very little to these Gas Solubility, and have limitation such as the big cost height of viscosity.The present invention is on the basis of considering the problems referred to above, adopts a class alcoholamine carboxylate ion liquid to absorb sour gas SO 2
Summary of the invention
The present invention adopts a class alcoholamine carboxylate ion liquid to absorb sour gas SO 2
The ionic liquid that is adopted among the present invention is an alcoholamine carboxylate ion liquid, be to be made of cations such as monoethanolamine, diethanol amine, triethanolamine or diglycolamine and acetate or lactic acid anion, and cationic anionic all is not limited to above-mentioned several.
In temperature range is under-50 ℃ to 20 ℃, and pressure absorbs SO with the synthetic ionic liquid of institute in normal pressure to 100 atmospheric pressure 2SO wherein 2Be pure SO 2Gas or contain SO 2Mist, ionic liquid is with the neat liquid form or load on form on other carriers.
The specific embodiment:
The present invention illustrates with following example, but the present invention is not limited to following embodiment, under the scope of described aim, changes and implements to be included in the technical scope of the present invention before and after not breaking away from.
Embodiment 1
Synthetic ion liquid experimental provision mainly is a there-necked flask, on put the condensing reflux pipe, and dropping funel and agitating device are housed, because the raw material viscosity of synthetic reaction is bigger, so stir with mechanical agitator.The monoethanolamine of accurate weighing is placed flask, and open agitator and stir, under high-speed stirred, dropwise drip lactic acid solution, the mole of lactic acid equates with monoethanolamine, drips off in 60 minutes.And at room temperature reacted 20 hours.At last with gained liquid 50 ℃ of dryings 48 hours in vacuum drying chamber, at last ionic liquid of ethanolamine lactate.
The ionic liquid of ethanolamine lactate of accurate weighing is placed an absorption bottle, and absorption bottle places 25 ℃ water bath with thermostatic control, is placed with stirring rotator in the absorption bottle, is placed with magnetic stirring apparatus under the absorption bottle.Speed with 5ml/min feeds SO in absorption bottle 2Gas is opened magnetic stirring apparatus simultaneously.The weighing absorption bottle heavily no longer changes visual its up to the absorption bottle weight and reaches balance at regular intervals.Reached balance in about 3 hours, the final SO that is absorbed that gets 2With the mol ratio of ionic liquid of ethanolamine lactate be 0.89.
Embodiment 2
Synthetic ion liquid experimental provision mainly is a there-necked flask, on put the condensing reflux pipe, and dropping funel and agitating device are housed, because the raw material viscosity of synthetic reaction is bigger, so stir with mechanical agitator.The monoethanolamine of accurate weighing is dissolved in absolute ethyl alcohol and places flask, and open agitator and stir, under high-speed stirred, dropwise drip the acetate ethanolic solution, the mole of acetate equates with monoethanolamine, drips off in 60 minutes.And at room temperature reacted 20 hours.Reaction finishes the back rotary evaporation and removes most of solvent, at last with gained liquid 50 ℃ of dryings 48 hours in vacuum drying chamber, at last the monoethanolamine acetate.
The monoethanolamine acetate ion liquid of accurate weighing is placed an absorption bottle, and absorption bottle places 25 ℃ water bath with thermostatic control, is placed with stirring rotator in the absorption bottle, is placed with magnetic stirring apparatus under the absorption bottle.Speed with 5ml/min feeds SO in absorption bottle 2Gas is opened magnetic stirring apparatus simultaneously.The weighing absorption bottle heavily no longer changes visual its up to the absorption bottle weight and reaches balance at regular intervals.Reached balance in about 3 hours, final the SO that absorbs 2With the mol ratio of monoethanolamine acetate ion liquid be 1.85.
Embodiment 3
Synthetic ion liquid experimental provision mainly is a there-necked flask, on put the condensing reflux pipe, and dropping funel and agitating device are housed, because the raw material viscosity of synthetic reaction is bigger, so stir with mechanical agitator.The triethanolamine of accurate weighing is placed flask, and open agitator and stir, under high-speed stirred, dropwise drip lactic acid solution, the mole of lactic acid equates with the mole of triethanolamine, dripped off in 60 minutes.And at room temperature reacted 20 hours.At last with gained liquid 50 ℃ of dryings 48 hours in vacuum drying chamber, at last the triethanolamine lactate.
The triethanolamine lactate ions liquid of accurate weighing is placed an absorption bottle, and absorption bottle places 25 ℃ water bath with thermostatic control, is placed with stirring rotator in the absorption bottle, is placed with magnetic stirring apparatus under the absorption bottle.Speed with 5ml/min feeds SO in absorption bottle 2Gas is opened magnetic stirring apparatus simultaneously.The weighing absorption bottle heavily no longer changes visual its up to the absorption bottle weight and reaches balance at regular intervals.Reached balance in about 3 hours, final the SO that absorbs 2With the mol ratio of triethanolamine lactate ions liquid be 0.98.
Embodiment 4
Synthetic ion liquid experimental provision mainly is a there-necked flask, on put the condensing reflux pipe, and dropping funel and agitating device are housed, because the raw material viscosity of synthetic reaction is bigger, so stir with mechanical agitator.The triethanolamine of accurate weighing is dissolved in absolute ethyl alcohol and places flask, and open agitator and stir, under high-speed stirred, dropwise drip the ethanolic solution of acetate, the mole of acetate equates with the mole of triethanolamine, dripped off in 60 minutes.And at room temperature reacted 20 hours.Reaction finishes the back rotary evaporation and removes most of solvent, at last with gained liquid 50 ℃ of dryings 48 hours in vacuum drying chamber, at last the triethanolamine acetate.
The triethanolamine acetate ion liquid of accurate weighing is placed an absorption bottle, and absorption bottle places 25 ℃ water bath with thermostatic control, is placed with stirring rotator in the absorption bottle, is placed with magnetic stirring apparatus under the absorption bottle.Speed with 5ml/min feeds SO in absorption bottle 2Gas is opened magnetic stirring apparatus simultaneously.The weighing absorption bottle heavily no longer changes visual its up to the absorption bottle weight and reaches balance at regular intervals.Reached balance in about 3 hours, final the SO that absorbs 2With the mol ratio of triethanolamine acetate ion liquid be 1.91.

Claims (7)

1. one kind absorbs SO with alcoholamine carboxylate ion liquid 2The method of gas is characterized in that alcoholamine carboxylate ion liquid is applied to absorb SO 2Gas.
2. method according to claim 1, the ion liquid cation of employing is cations such as monoethanolamine, diethanol amine, triethanolamine or diglycolamine.
3. method according to claim 1, adopting ion liquid anion is acetate ion or lactate ion.
4. method according to claim 1, alcoholamine carboxylate ion liquid absorbs SO 2Temperature range be-50 ℃ to 20 ℃.
5. method according to claim 1, alcoholamine carboxylate ion liquid absorbs SO 2Pressure limit within normal pressure to 100 atmospheric pressure.
6. method according to claim 1, the SO that such ionic liquid absorbs 2Be pure SO 2Gas and contain SO 2Mist.
7. method according to claim 1, such ionic liquid absorbs SO with neat liquid form and the form that loads on other carriers 2
CNB2005100694066A 2005-05-09 2005-05-09 Method for absorbing SO2 gas by alcoholamine carboxylate ion liquid Expired - Fee Related CN1327934C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB2005100694066A CN1327934C (en) 2005-05-09 2005-05-09 Method for absorbing SO2 gas by alcoholamine carboxylate ion liquid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB2005100694066A CN1327934C (en) 2005-05-09 2005-05-09 Method for absorbing SO2 gas by alcoholamine carboxylate ion liquid

Publications (2)

Publication Number Publication Date
CN1698928A CN1698928A (en) 2005-11-23
CN1327934C true CN1327934C (en) 2007-07-25

Family

ID=35475278

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB2005100694066A Expired - Fee Related CN1327934C (en) 2005-05-09 2005-05-09 Method for absorbing SO2 gas by alcoholamine carboxylate ion liquid

Country Status (1)

Country Link
CN (1) CN1327934C (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101537300B (en) * 2009-04-17 2011-08-10 合肥工业大学 Recyclable sulfur dioxide gas absorbent and preparation method thereof

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2444614A (en) * 2005-09-30 2008-06-11 Bioniqs Ltd Alkanoyl ammonium salts as ionic liquids
CN101628876B (en) * 2008-07-15 2012-07-04 南京理工大学 Method for synthesizing ionic liquid of ethanolamine lactate
CN102516092A (en) * 2011-12-14 2012-06-27 南京大学扬州化学化工研究院 Dicarboxylic hydrogen salt ionic liquid with asymmetric chemical structure and weak acidity, and preparation method thereof
CN102911151B (en) * 2012-07-12 2014-10-22 盐城师范学院 Method for water-phase synthesis of benzoxanthene derivatives
CN103007688B (en) * 2012-12-24 2014-09-24 中国科学院过程工程研究所 Ion solvent for absorbing and separating SO2 in industrial gases
CN103432864B (en) * 2013-07-09 2016-09-28 南京信息工程大学 A kind of absorb the organic solution of sulfur dioxide in gaseous mixture
CN103521036B (en) * 2013-10-10 2015-10-28 浙江大学 A kind of method adopting metal chelate ionic liquid capture sulfur dioxide
CN104162342B (en) * 2014-08-18 2016-04-20 南京信息工程大学 A kind of compound ionic liquid desulfurization and decarburization agent and its preparation method and application
CN104402733A (en) * 2014-09-30 2015-03-11 河北科技大学 Low-carbon straight-chain primary amine ionic liquid used for absorbing SO2 and preparation method and application thereof
CN105727888A (en) * 2014-12-11 2016-07-06 中国石油化工股份有限公司 Reproducible SO2 adsorbent and preparation method therefor
CN105194982A (en) * 2015-10-14 2015-12-30 黄锐 Ionic liquid capable of absorbing sulfur dioxide as well as preparation method and application of ionic liquid
CN106854478A (en) * 2015-12-08 2017-06-16 中国石油化工股份有限公司 A kind of absorbing liquid containing ionic liquid activator
CN113233989B (en) * 2021-05-27 2022-07-29 湖南西林环保材料有限公司 1, 4-trihydroxyethylbenzdiammonium sulfate, 1,3, 5-trihydroxyethylbenztriammonium sulfate, synthesis and application thereof

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1385243A (en) * 2002-06-07 2002-12-18 华东师范大学 Diacetone acrylic amide type ionic liquid and preparation thereof

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1385243A (en) * 2002-06-07 2002-12-18 华东师范大学 Diacetone acrylic amide type ionic liquid and preparation thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101537300B (en) * 2009-04-17 2011-08-10 合肥工业大学 Recyclable sulfur dioxide gas absorbent and preparation method thereof

Also Published As

Publication number Publication date
CN1698928A (en) 2005-11-23

Similar Documents

Publication Publication Date Title
CN1327934C (en) Method for absorbing SO2 gas by alcoholamine carboxylate ion liquid
CN1698929A (en) Functionalized ion liquid of alcoholamine carboxylate
CN105597492B (en) The removing method and sour gas removing device of acid gas absorbent, sour gas
Xiong et al. Selective separation of aliphatic and aromatic amines with CO 2 switchable ionic liquids aqueous two-phase systems
Tzani et al. Synthesis and structure-properties relationship studies of biodegradable hydroxylammonium-based protic ionic liquids
Keshav et al. Reactive extraction of propionic acid using tri‐n‐octylamine, tri‐n‐butyl phosphate and aliquat 336 in sunflower oil as diluent
CN104370952A (en) Organic-ligand-based multifunctional zinc complexes and application thereof
CN108794400A (en) A kind of ionic liquid and its preparation method and application containing amino acid of the cation with amino
Zhang et al. Energy-saving effect of low-cost and environmentally friendly sepiolite as an efficient catalyst carrier for CO2 capture
CN101537300B (en) Recyclable sulfur dioxide gas absorbent and preparation method thereof
CN102451597A (en) Ion liquid solution for collecting carbon dioxide
CN101537304A (en) Cyclic amine sulfur dioxide gas absorbent and preparation method thereof
CN102794082B (en) Mixed solvent for trapping carbon dioxide
Wen et al. Novel amino acid ionic liquids as messenger of multi-tertiary-amines solutions for highly efficient capture of CO2
CN102548640A (en) Carbon dioxide absorbent solution
CN102527247A (en) Strong acid and strong alkali resistance organic tubular membrane and preparation method thereof, and membrane casting liquid
He et al. Antimicrobial ionic liquids with fumarate anion
CN102029115A (en) Preparation method of ethanol pervaporation hybrid film used for removing methyl alcohol in wastewater
CN102019128A (en) Method for absorbing hydrogen chloride through ionic liquid
CN101456875A (en) Hydrogen bond type rare-earth metal complexes and preparation method thereof
CN105017045A (en) Bis-quaternary ammonium salt with linking groups that contain diester groups and application thereof as bactericide
Hao et al. Low viscous aminoalkyl‐phenyl‐silane with π–π interaction and its optimal SO2 capture condition
Sakakura et al. Unusual Rate Acceleration in Brønsted Acid Catalyzed Dehydration Reactions: Local Hydrophobic Environment in Aggregated N‐(2, 6‐diphenylphenyl)‐N‐mesitylammonium Pentafluorobenzenesulfonates
Canari et al. Effect of pH on dicarboxylic acids extraction by amine-based extractants
CN102600700A (en) Preparation method and application of ionic liquid type absorbent

Legal Events

Date Code Title Description
C06 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
ASS Succession or assignment of patent right

Owner name: BEIJING ZHONGKE ANYIN TECHNOLOGY. CO., LTD.

Free format text: FORMER OWNER: INST. OF PROCESS ENGRG., CHINESE ACADEMY OF SCIENCES

Effective date: 20120410

C41 Transfer of patent application or patent right or utility model
COR Change of bibliographic data

Free format text: CORRECT: ADDRESS; FROM: 100080 HAIDIAN, BEIJING TO: 102200 CHANGPING, BEIJING

TR01 Transfer of patent right

Effective date of registration: 20120410

Address after: 102200 Zhongxing Road 10, Changping District science and Technology Park, Beijing

Patentee after: Beijing Zhongke Neiyin AI Technology Co. Ltd.

Address before: 100080 No. two, No. 1, North Haidian District, Beijing, Zhongguancun

Patentee before: Institute of Process Engineering, Chinese Academy of Sciences

DD01 Delivery of document by public notice

Addressee: Beijing Zhongke Neiyin AI Technology Co. Ltd. Zhao Lidong

Document name: Notification of Passing Examination on Formalities

C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20070725

Termination date: 20140509

DD01 Delivery of document by public notice

Addressee: Zhao Lidong

Document name: Notification of Termination of Patent Right