WO2010057597A2 - Procédé et installation pour récupérer le nh3 à partir d'un mélange contenant du nh3 et des gaz acides - Google Patents

Procédé et installation pour récupérer le nh3 à partir d'un mélange contenant du nh3 et des gaz acides Download PDF

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Publication number
WO2010057597A2
WO2010057597A2 PCT/EP2009/008113 EP2009008113W WO2010057597A2 WO 2010057597 A2 WO2010057597 A2 WO 2010057597A2 EP 2009008113 W EP2009008113 W EP 2009008113W WO 2010057597 A2 WO2010057597 A2 WO 2010057597A2
Authority
WO
WIPO (PCT)
Prior art keywords
gas absorber
sour gas
stripping column
sour
absorber
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.)
Ceased
Application number
PCT/EP2009/008113
Other languages
German (de)
English (en)
Other versions
WO2010057597A3 (fr
Inventor
Gert Ungar
Matthias Linicus
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.)
Air Liquide Global E&C Solutions Germany GmbH
Original Assignee
Lurgi GmbH
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 Lurgi GmbH filed Critical Lurgi GmbH
Priority to EP09760100.9A priority Critical patent/EP2385929B1/fr
Priority to AU2009317550A priority patent/AU2009317550B2/en
Priority to CN200980145675.2A priority patent/CN102216217B/zh
Priority to RU2011124501/05A priority patent/RU2491228C2/ru
Priority to US13/130,258 priority patent/US8821822B2/en
Priority to MX2011005219A priority patent/MX2011005219A/es
Publication of WO2010057597A2 publication Critical patent/WO2010057597A2/fr
Publication of WO2010057597A3 publication Critical patent/WO2010057597A3/fr
Priority to ZA2011/03519A priority patent/ZA201103519B/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01C—AMMONIA; CYANOGEN; COMPOUNDS THEREOF
    • C01C1/00—Ammonia; Compounds thereof
    • C01C1/02—Preparation, purification or separation of ammonia
    • C01C1/12—Separation of ammonia from gases and vapours
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D53/00—Separation 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
    • B01D53/14—Separation 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 by absorption
    • B01D53/1425—Regeneration of liquid absorbents
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D53/00—Separation 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
    • B01D53/14—Separation 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 by absorption
    • B01D53/1456—Removing acid components
    • B01D53/1462—Removing mixtures of hydrogen sulfide and carbon dioxide
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B17/00—Sulfur; Compounds thereof
    • C01B17/16—Hydrogen sulfides
    • C01B17/167—Separation
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01C—AMMONIA; CYANOGEN; COMPOUNDS THEREOF
    • C01C1/00—Ammonia; Compounds thereof
    • C01C1/02—Preparation, purification or separation of ammonia
    • C01C1/024—Purification
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01C—AMMONIA; CYANOGEN; COMPOUNDS THEREOF
    • C01C1/00—Ammonia; Compounds thereof
    • C01C1/02—Preparation, purification or separation of ammonia
    • C01C1/10—Separation of ammonia from ammonia liquors, e.g. gas liquors
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2251/00—Reactants
    • B01D2251/20—Reductants
    • B01D2251/206—Ammonium compounds
    • B01D2251/2062—Ammonia
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2257/00—Components to be removed
    • B01D2257/30—Sulfur compounds
    • B01D2257/304—Hydrogen sulfide
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2257/00—Components to be removed
    • B01D2257/50—Carbon oxides
    • B01D2257/504—Carbon dioxide
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D53/00—Separation 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
    • B01D53/34—Chemical or biological purification of waste gases
    • B01D53/74—General processes for purification of waste gases; Apparatus or devices specially adapted therefor
    • B01D53/77—Liquid phase processes
    • Y—GENERAL 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
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/151—Reduction of greenhouse gas [GHG] emissions, e.g. CO2

Definitions

  • the present invention relates to a method and a plant for the production of NH 3 from a NH 3 , H 2 S- and / or CO 2 -containing acid gas and low-boiling water-soluble organic components having mixture, in particular wastewater.
  • a bottom product containing all the sour gases, which originate from the Entklaterumpf. This requires a relatively low NH 3 excess.
  • the top product consists of NH 3 , which still contains acid gases in low concentration.
  • the sour gases are absorbed in aqueous NH 3 from the acid-containing NH 3 .
  • the bottom product of the NH 3 -Absreibers is supplied to the Entklarer. On the head of Entklarers pure water is added which can also originate from the bottom of Totalabtreibers to get out of the acid gas to absorb NH 3 in full.
  • the bottom product of the decanter is fed to the totalizer whose top product is fed into the bottom of the sour gas absorber.
  • the bottom product is NH 3 and CO 2 -free wastewater.
  • EP 1 135 331 B1 differs from the process described at the beginning in that the overhead vapors of the overhead dispersions are condensed, with the liquid being led into the NH 3 vaporiser.
  • volatile water-soluble organic components in particular in the sour gas absorber, can accumulate to such an extent that the processes no longer function.
  • This object is achieved in that a partial stream of the liquid phase is withdrawn from the sour gas absorber and worked up so that you get gaseous NH 3 with a reduced content of volatile organic components, which is attributed to the sour gas absorber.
  • the content of volatile water-soluble organic components in the liquid phase of the sour gas absorber can be limited by the process according to the invention such that they do not disturb the smooth flow.
  • Components of the withdrawn from the acid gas absorber liquid phase may be discharged from the process and sent for disposal.
  • the process is suitable if the low-boiling water-soluble organic components contain alcohols, ketones, nitriles and / or pyridine bases.
  • the partial stream withdrawn from the suction gas absorber is fed to a first stripping column in which all volatile components are largely driven off.
  • the top product of the stripping column is partially condensed and the remaining vapors are recycled to the sour gas absorber.
  • the partial condensate obtained is preferably fed to a further stripping column, in which NH 3 and sour gases are driven off so far that the organic components in the bottoms are concentrated.
  • the top product of the second stripping column whose proportion of volatile organic compounds is correspondingly further reduced, is recycled to the sour gas absorber.
  • the separation of volatile organic compounds via one or more stripping columns is particularly effective when the stripping column (s) are each operated at a pressure of 2 to 20 bar.
  • the pressure is adjusted to 4 to 16 bar, more preferably to about 6.5 bar.
  • the bottom product of the second stripping column can be expanded to the pressure of the acid gas absorber and mixed with the bottom product of a column in which the NH 3 is purified, for example by distillation. Relaxation vapors are supplied in this case the sour gas absorber.
  • the NH 3 which is largely freed from acid gas at the top of the sour gas absorber, is preferably supplied to further purification stages and / or liquefied.
  • the aqueous NH 3 conducted to the sour gas absorber which serves as absorption medium, is split up.
  • a portion of the aqueous NH 3 is applied to the head of the sour gas absorber and a portion of the aqueous NH 3 is fed to the lowermost absorption loop of the sour gas absorber.
  • the present invention relates to a plant for the recovery of NH 3 , which is particularly suitable for carrying out the method described above.
  • the plant has an acid gas absorber operated with aqueous NH 3 , the acid gas absorber being followed by a first stripping column, to which a substream of the liquid phase from the sour gas absorber is fed, and wherein the head of the first stripping column is mixed with the sour gas absorber.
  • Absorber is connected.
  • the plant according to the invention has, according to a preferred embodiment, a further stripping column to which the partial condensate is fed to the first stripping column and further driven off in the NH 3 and acid ergase, the head of the further stripping column being connected to the sour gas absorber is.
  • the withdrawn from the sour gas absorber NH 3 is liquefied in a condenser, wherein according to a further feature of the invention, the condenser is connected via return lines to the head of the sour gas absorber.
  • An inventive embodiment of the plant is that the NH 3 - stripping column is connected via a line to the first stripping column to be able to direct a liquid or vapor partial stream from the NH 3 -Abreteskolonne to the first stripping column.
  • FIG. 1 shows a process flow diagram of a plant for obtaining NH 3 from a mixture containing NH 3 and sour gases according to a preferred embodiment of the present invention.
  • a wastewater to be treated which is usually a condensate from the degasification or gasification of coal, is introduced in line 1.
  • the wastewater is treated with stripping gas from the line 3, further stripping gas comes from the lines 58 and 4.
  • the loaded stripping gas leaves the column 2 via line 5 and is fed to a workup, not shown.
  • the aborted in the Totalabtriebskolonne 8 gases pass through the gas-permeable bottom 11 upwards into the partial condenser 12, in which they are sprinkled with circulating cooled condensate to condense especially water vapor.
  • the condensate flows via line 13 under the action of a pump, not shown, through an outer cooler 14 and returns in the line 15 back into the sub-capacitor 12.
  • Sige condensate is supplied through the overflow 16 of the total stripping column 8.
  • the top product of the total stripping column 8 leaves the partial condenser 12 in the line 17 and enters a further condenser 18, in which an intensive cooling takes place, so that a liquid phase is formed.
  • the condenser 18 has a liquid circulation through the lines 19, 20 and 21, wherein an external cooler 22 keeps the temperature low.
  • the liquid phase of the condenser 18 does not receive inert gases such as N 2 , H 2 , CO and CH 4 . These drain in the line 4 and serve in the column 2 as additional stripping gases.
  • a partial flow of the liquid phase from the line 19 is withdrawn via line 23 and a NH 3 -Abtriebskolonne 24, in the bottom of a reboiler 25 is disposed abandoned.
  • the NH 3 -Abreteskolonne has, for example, ten to thirty trays, wherein the liquid phase from the line 23 approximately on a central floor supplies.
  • the top product of the NH 3 -Abreteskolonne 24, a NH 3 -rich gas containing residues of acid gases is first supplied to the acid gas absorber 27 in the first washing stage 28 in line 26. This is equipped with an absorption cycle with the lines 29, 30 and 31 with external cooler 32.
  • a partial stream of the absorbate passes from the bottom of the sour gas absorber 27 through the line 33 as reflux to the top of the NH 3 -Abtriebskolonne 24.
  • About the washing stage 28 of the sour gas absorber 27 are a second washing stage 34 and a third washing stage 35, between which a bottom 36 is arranged, which passes gas up and liquid down.
  • the third washing stage 35 is equipped with an absorption circuit with the lines 37, 38 and 39 and the external cooler 40. From the third washing stage 35 reaches virtually pure NH 3 via line 41 to the NH 3 liquefied 42. Via line 43, liquid NH 3 and via line 44 organic components from the NH 3 liquefied 42 are discharged.
  • the NH 3 liquefier 42 clean water over Line 45 is supplied.
  • the absorption liquid of the sour gas absorber 27 is aqueous NH 3 from the NH 3 liquefied 42, which is discharged via line 46 and fed to a part via line 47 in the line 37 and the washing stage 35 is fed and the other part via line 48th into the line 30 of the absorption cycle of the washing stage 28 is fed.
  • the withdrawn from the bottom of the NH 3 -Abreteskolonne 24 water flows in line 49 under the action of a pump, not shown, first to a heat exchanger 50 and enters through the line 51 in the Entcicsko- lonne 52, in which by means of the Aufkochers 53 a aborted to NH 3 , CO 2 and H 2 S rich gas mixture.
  • the withdrawn via line 6 from the bottom of the column 2 water flows after passing through the heat exchanger 55 via lines 54 and 56 to the deacidification column 52. Further above is discharged via line 57 from the Totalabtriebskolonne 8 discharged cooled water in the Entklarungskolonne.
  • the gas mixture is washed before it is passed via the line 58 for further processing as stripping gas to the column 2.
  • the deacidification column 52 falls as the bottom product deacidified water containing NH 3 and lower amounts of CO 2 and H 2 S contains.
  • This bottom product is withdrawn in the line 59 and initially releases some of its heat in the heat exchanger 50 and then passes via the lines 60 and 61 partially into the total output column 8.
  • a controllable by the valve 62 partial flow is discharged in the line 63 and the liquid phase which flows in the lines 19, 20 from the condenser column 18, admixed.
  • a portion of the liquid phase of the acid gas absorber 27 is supplied via the line 64 to a first stripping column 65, in which NH 3 , sour gases and volatile organic components are largely driven off.
  • the bottom product of the first stripping column 65 is passed via the line 66 to a lower bottom of the total stripping column 8.
  • the top product of the first stripping column 65 is fed via the line 67 to a condenser 68 and cooled to a recoverable with cooling water temperature. Most of the water and organic components are condensed and some of the NH 3 and sour gases are absorbed.
  • the vapors are returned via the line 69 in the sour gas absorber 27 and the liquid phase via the line 70 of a second stripper column 71 abandoned in the NH 3 and sour gases are driven off so far that the organic components are concentrated in the sump and only one small part leave the stripping column 71 with the top product.
  • the overhead product is passed via line 72 back into the sour gas absorber 27.
  • a portion of the recirculated over the line 46 recirculated, aqueous NH 3 is branched off and not via the lines 47 and 39 the head of the sour gas absorber 27, but via the lines 48, 30 and 31 and via the external cooler 32nd the lower absorption cycle of the sour gas absorber 27 is supplied.
  • 27 total concentrations of the organic components in the liquid phase of the sour gas absorber 27 of 17.5 wt .-% can be achieved by supplying the aqueous NH 3 as an absorbent exclusively to the head of the sour gas absorber the concentration can be reduced to 9.5 wt .-% at the introduction of a partial flow in the lower absorption cycle of the sour gas absorber 27.
  • the bottom product of the second stripping column 71 can be expanded to the pressure of the acid gas absorber 27 via the conduit 73 for further disposal or, after it has been previously mixed with the cooled bottom product of a column in which the NH 3 is purified, for example by distillation , The flash steam is then also supplied to the acid gas absorber 27.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Analytical Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Gas Separation By Absorption (AREA)
  • Treating Waste Gases (AREA)
  • Industrial Gases (AREA)

Abstract

La présente invention porte sur un procédé et une installation pour récupérer de l'ammoniac à partir d'un mélange comportant de l'ammoniac, du H2S et/ou un gaz acide contenant du CO2, ainsi que des composants organiques solubles dans l'eau et à bas point d'ébullition. Pour éviter un enrichissement des composés organiques volatils dans l'absorbeur de gaz acide, on soutire un courant partiel de la phase liquide à partir d'un absorbeur de gaz acide, et on le traite de façon à obtenir de l'ammoniac gazeux ayant une teneur réduite en composants organiques volatils, qui est renvoyé dans l'absorbeur de gaz acide.
PCT/EP2009/008113 2008-11-20 2009-11-13 Procédé et installation pour récupérer le nh3 à partir d'un mélange contenant du nh3 et des gaz acides Ceased WO2010057597A2 (fr)

Priority Applications (7)

Application Number Priority Date Filing Date Title
EP09760100.9A EP2385929B1 (fr) 2008-11-20 2009-11-13 Procede et installation pour recuperer le nh3 a partir d'un melange contenant du nh3 et des gaz acides
AU2009317550A AU2009317550B2 (en) 2008-11-20 2009-11-13 Method and plant for obtaining NH3 from a mixture comprising NH3 and acidic gases
CN200980145675.2A CN102216217B (zh) 2008-11-20 2009-11-13 从包含nh3和酸性气体的混合物中获得nh3的方法和装置
RU2011124501/05A RU2491228C2 (ru) 2008-11-20 2009-11-13 Способ и установка для получения nh3 из содержащей nh3 и кислые газы смеси
US13/130,258 US8821822B2 (en) 2008-11-20 2009-11-13 Process and plant for recovering NH3 from a mixture comprising NH3 and acid gases
MX2011005219A MX2011005219A (es) 2008-11-20 2009-11-13 Proceso y planta para recuperar nh3 a partir de una mezcla que contiene nh3 y gases acidos.
ZA2011/03519A ZA201103519B (en) 2008-11-20 2011-05-13 Method and plant for obtaining nh3 from a mixture comprising nh3 and acidic gaseous

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102008058143.7 2008-11-20
DE102008058143A DE102008058143B4 (de) 2008-11-20 2008-11-20 Verfahren und Anlage zur Gewinnung von NH3 aus einem NH3 und Sauergase enthaltenden Gemisch

Publications (2)

Publication Number Publication Date
WO2010057597A2 true WO2010057597A2 (fr) 2010-05-27
WO2010057597A3 WO2010057597A3 (fr) 2011-03-24

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2009/008113 Ceased WO2010057597A2 (fr) 2008-11-20 2009-11-13 Procédé et installation pour récupérer le nh3 à partir d'un mélange contenant du nh3 et des gaz acides

Country Status (9)

Country Link
US (1) US8821822B2 (fr)
EP (1) EP2385929B1 (fr)
CN (1) CN102216217B (fr)
AU (1) AU2009317550B2 (fr)
DE (1) DE102008058143B4 (fr)
MX (1) MX2011005219A (fr)
RU (1) RU2491228C2 (fr)
WO (1) WO2010057597A2 (fr)
ZA (1) ZA201103519B (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103387271A (zh) * 2013-07-16 2013-11-13 大连理工大学 一种化产蒸氨和脱硫的热集成装置

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CN102688607B (zh) * 2012-05-24 2015-06-03 崇义章源钨业股份有限公司 氨尾气回收利用的方法和系统
BR112015022004B8 (pt) * 2013-03-15 2022-07-12 Mecs Inc Processos para remoção de gás contaminante da fonte de gás e recuperação do referido gás e para a remoção de dióxido de enxofre de fonte de gás contendo dióxido de enxofre e recuperação do dióxido de enxofre
US10005021B1 (en) * 2016-12-22 2018-06-26 General Electric Technology Gmbh System and method for recovering ammonia from a gas stream
CN107684814A (zh) * 2017-10-23 2018-02-13 张家港市艾尔环保工程有限公司 去除废气中无机气体的方法
CN108554324B (zh) * 2017-12-29 2021-01-08 南京理工大学 一种基于化学链反应制备氨气的装置及方法
CN108383309B (zh) * 2018-03-02 2021-02-09 中国成达工程有限公司 一种煤化工变换酸性冷凝液提氨系统及提氨工艺
CN109248564B (zh) * 2018-11-15 2021-01-05 山东海科化工集团有限公司 一种石化炼厂酸性水处理装置产生的粗氨水的回收利用装置和工艺
RU2756955C1 (ru) * 2020-10-26 2021-10-07 Акционерное общество "Газпромнефть - Омский НПЗ" (АО "Газпромнефть-ОНПЗ") Способ очистки аммиаксодержащего газа и получения безводного жидкого аммиака
CN112441641A (zh) * 2020-11-20 2021-03-05 南京敦先化工科技有限公司 一种多塔串联废水蒸氨环保处理方法
IT202100005585A1 (it) * 2021-03-10 2022-09-10 Nuovo Pignone Tecnologie Srl Sistema di abbattimento di biossido di carbonio a base di ammoniaca con sezioni sovrapposte

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Publication number Priority date Publication date Assignee Title
CN103387271A (zh) * 2013-07-16 2013-11-13 大连理工大学 一种化产蒸氨和脱硫的热集成装置

Also Published As

Publication number Publication date
DE102008058143A1 (de) 2010-05-27
EP2385929B1 (fr) 2018-05-23
RU2011124501A (ru) 2012-12-27
WO2010057597A3 (fr) 2011-03-24
CN102216217A (zh) 2011-10-12
MX2011005219A (es) 2011-06-16
RU2491228C2 (ru) 2013-08-27
AU2009317550A1 (en) 2011-07-14
AU2009317550B2 (en) 2013-06-27
ZA201103519B (en) 2012-09-26
US20110278152A1 (en) 2011-11-17
DE102008058143B4 (de) 2012-04-12
EP2385929A2 (fr) 2011-11-16
CN102216217B (zh) 2015-12-02
AU2009317550A2 (en) 2011-07-21
US8821822B2 (en) 2014-09-02

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