WO2009024612A1 - Method for the cleaning of off-gas - Google Patents

Method for the cleaning of off-gas Download PDF

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Publication number
WO2009024612A1
WO2009024612A1 PCT/EP2008/061013 EP2008061013W WO2009024612A1 WO 2009024612 A1 WO2009024612 A1 WO 2009024612A1 EP 2008061013 W EP2008061013 W EP 2008061013W WO 2009024612 A1 WO2009024612 A1 WO 2009024612A1
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WO
WIPO (PCT)
Prior art keywords
scrubber
scrubber stage
stage
gas
separation
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/EP2008/061013
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English (en)
French (fr)
Inventor
Hans Hunsinger
Martin Karlsson
Sven Andersson
Ulf HÄGG
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.)
Karlsruher Institut fuer Technologie KIT
Gotaverken Miljo AB
Original Assignee
Forschungszentrum Karlsruhe GmbH
Gotaverken Miljo AB
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 Forschungszentrum Karlsruhe GmbH, Gotaverken Miljo AB filed Critical Forschungszentrum Karlsruhe GmbH
Priority to EP08827917.9A priority Critical patent/EP2180938B1/en
Priority to KR1020107006362A priority patent/KR101535280B1/ko
Priority to CN200880104087XA priority patent/CN101842147B/zh
Priority to RU2010110637/05A priority patent/RU2488431C2/ru
Priority to JP2010521439A priority patent/JP5455907B2/ja
Priority to CA2696199A priority patent/CA2696199C/en
Priority to DK08827917.9T priority patent/DK2180938T3/da
Priority to US12/733,314 priority patent/US8048392B2/en
Priority to PL08827917T priority patent/PL2180938T3/pl
Publication of WO2009024612A1 publication Critical patent/WO2009024612A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • 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
    • B01D53/46—Removing components of defined structure
    • B01D53/48—Sulfur compounds
    • B01D53/50—Sulfur oxides
    • 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
    • B01D53/46—Removing components of defined structure
    • B01D53/48—Sulfur compounds
    • B01D53/50—Sulfur oxides
    • B01D53/501—Sulfur oxides by treating the gases with a solution or a suspension of an alkali or earth-alkali or ammonium compound
    • B01D53/502—Sulfur oxides by treating the gases with a solution or a suspension of an alkali or earth-alkali or ammonium compound characterised by a specific solution or suspension
    • 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
    • B01D53/38—Removing components of undefined structure
    • B01D53/40—Acidic components
    • 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
    • B01D53/46—Removing components of defined structure
    • B01D53/64—Heavy metals or compounds thereof, e.g. mercury
    • 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
    • B01D53/46—Removing components of defined structure
    • B01D53/68—Halogens or halogen compounds
    • 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
    • B01D53/75—Multi-step processes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2251/00—Reactants
    • B01D2251/10—Oxidants
    • B01D2251/106—Peroxides
    • 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
    • B01D2251/00—Reactants
    • B01D2251/60—Inorganic bases or salts
    • B01D2251/604—Hydroxides
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2257/00—Components to be removed
    • B01D2257/20—Halogens or halogen compounds
    • B01D2257/204—Inorganic halogen compounds
    • B01D2257/2045—Hydrochloric acid
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2257/00—Components to be removed
    • B01D2257/20—Halogens or halogen compounds
    • B01D2257/204—Inorganic halogen compounds
    • B01D2257/2047—Hydrofluoric acid
    • 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
    • B01D2257/302—Sulfur oxides
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2257/00—Components to be removed
    • B01D2257/60—Heavy metals or heavy metal compounds
    • B01D2257/602—Mercury or mercury compounds
    • 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
    • Y02C—CAPTURE, STORAGE, SEQUESTRATION OR DISPOSAL OF GREENHOUSE GASES [GHG]
    • Y02C20/00—Capture or disposal of greenhouse gases
    • Y02C20/30—Capture or disposal of greenhouse gases of perfluorocarbons [PFC], hydrofluorocarbons [HFC] or sulfur hexafluoride [SF6]

Definitions

  • the present invention concerns a method and a device for the cleaning of flue gases, in particular for the separation of sulphur dioxide (SO2) from flue gas and at the same time prevention of the releasing of ammonia (NH3) and the formation of aerosols at ammonium sulphate resulting therefrom.
  • SO2 sulphur dioxide
  • NH3 ammonia
  • EP 0 778 067 B1 discloses a device for the cleaning of smoke gases with different amounts of acidic components and methods for the operation of the device. After a dust filter and a quench/scrubber step for the separation of hydrochloric acid and hydrofluoric acid by washing with water a counter current scrubber process for the separation of sulphur dioxide is arranged.
  • EP 0 212 523 discloses a one-stage counter current scrubber process with the addition of ammonia and oxidation to sulphate by means of addition of air in the scrubber bottom.
  • the object of the present invention therefore is to provide a method for the efficient separation of sulphur dioxide from off-gases and at the same time avoiding the release of ammonia and the formation of aerosol of ammonium sulphate resulting therefrom.
  • This problem is solved by a process comprising the following steps:
  • Sulphur dioxide is separated from off-gas in a first scrubber stage by means of ammonia or ammonium compounds,
  • the off-gas is transferred into a second scrubber stage, 3. in the second scrubber stage the sulphur dioxide, which has not been separated in the first scrubber stage, is oxidised by addition of an oxidizing agent, for example hydrogen peroxide to sulphuric acid and separated
  • an oxidizing agent for example hydrogen peroxide to sulphuric acid
  • the ammonia released from the first scrubber stage is separated in the second scrubber stage together with the formed sulphuric acid via formation of ammonium sulphate.
  • the method according to the invention therefore consists of a two-stage scrubber combination, a part of the sulphur dioxide being separated by ammonia in the first scrubber stage and in the second stage the sulphur dioxide, which has not been separated in the first scrubber stage, being separated by means of an oxidizing agent, in particular hydrogen peroxide being used as oxidizing agent.
  • an oxidizing agent preferably hydrogen peroxide
  • the addition of an oxidizing agent, preferably hydrogen peroxide is done at least in an stoichiometric amount in view of the S ⁇ 2-charge entering the second scrubber stage.
  • Particularly preferred is a slightly increased amount of oxidizing agent in view of the charge of sulphur dioxide entering the second scrubber-stage.
  • Both scrubber stages may be provided with one or more wet scrubber cycles. The wet scrubber cycles within a scrubber stage may each have an own or a common bottom.
  • the scrubber solutions (washing water discharge) of the respective scrubber stages can be led counter-currently to the off-gas.
  • the sulphuric acid/ammonium sulphate-solution mixture formed in the second scrubber-stage and the excess of hydrogen peroxide present therein is fed back into the preset first scrubber-stage.
  • ammonia is added, preferably in form of an aqueous ammonia solution.
  • ammonia also other ammonium compounds such as ammonium carbonate are usable as well.
  • the pH-value decreases in the scrubber solution.
  • the pH- value is kept in a variable manner in a control-range of 4 to 6. Under these conditions, the sulphur dioxide in the off-gas is separated in a high proportion.
  • the typical separation rates for sulphur dioxide in one scrubber stage are at about 30 to 90% at pH-values of about 4 to 6.
  • a considerable oxidation of the primarily formed ammonium sulfite takes place by the oxygen being present in the smoke gas.
  • the effect of oxidation with oxygen can be maximised by intensive contact between smoke gas and scrubber fluid (large area of exchange of substances, high ratio of scrubber solution to off-gas).
  • the dispersion of 02-containing smoke gas or air in the wet scrubber cycle can contribute to a further increase of the oxidation degree.
  • the products are formed after the following reactions:
  • the ammonium sulfite or -sulphate solution, formed by the reaction is characterized by a ammonia partial pressure which is dependant from the pH-value and the temperature of the scrubber solution.
  • the partial pressure of ammonia decreases at lower pH- values. It is disadvantageous that the separation of sulphur dioxide decreases likewise with the decrease of the pH-value. At pH-values in the range of 4 to 6, a sufficiently high separation of sulphur dioxide and a moderate release of ammonia are ensured.
  • a molar concentration ratio of SO 2 to NH 3 in the off-gas after the first scrubber stage of 0.5 is preferable , more preferable in the range of 0.5 to 2, in particular preferable in the range of 0.5 to 1.
  • the molar concentration ratio SO 2 /NH 3 can be controlled via the pH-value in the second scrubber stage. I.e., the desired pH- value in the first scrubber stage is controlled via a cascade control based on the pH- value (difference of pH-value from desired value) of the second scrubber stage.
  • a decreasing pH-value in the second scrubber stage means an excess of SO 2 and an increasing pH-value an excess of NH 3 in the off-gas before entering the second scrubber stage.
  • the pH-value in the second scrubber stage is concretely set in the range of 1 to 5, preferably in the range of 2 to 4, the pH-value in the second scrubber stage for example is set at about 3. If the pH-value in the second scrubber stage falls below the specified value (for example pH ⁇ 3) the desired -pH-value in the first scrubber stage is automatically increased via a control loop. As a result the separation degree of SO 2 in the first scrubber stage and the release of NH 3 is increased. This results in the increasing of the pH-value in the second scrubber-stage. With increasing pH-value (for example pH>3) in the second scrubber-stage, the desired pH-value of the first scrubber-stage is decreased.
  • the specified value for example pH ⁇ 3
  • the two stage scrubber method can be optimally controlled, i.e. the pH-value in the second scrubber-stage is maintained at about 3 and thus the molar concentration ratio of SO2 to NH3 in the off-gas after the first scrubber-stage is maintained in the desired range of about for example 0.5-1.
  • the SO2 concentrations in the off-gas of technical processes, for example waste incinerators, can have considerable fluctuations as a result of the heterogeneous fuel compositions. This means that the optimal pH-value of the first scrubber stage cannot be a fixed value.
  • the optimal desired pH-value of the first scrubber stage therefore can vary within a relatively wide range of from about 4 to 6.
  • the regulation to the variable desired pH-value in the first scrubber-stage is done by means of a NH3 dosage into the scrubber-cycle of the first scrubber stage.
  • the off-gas is then transferred into the second scrubber stage.
  • an oxidizing agent is now added into the second scrubber stage.
  • the SO2 separation is by at least stoichiometrical addition of an oxidizing agent into the scrubber solution to a large extent independent from the pH-value.
  • Preferable is the addition of hydrogen peroxide as oxidizing agent.
  • other oxidizing agents such as for example ozone, sodium or potassium peroxide may be considered.
  • the required amount of oxidizing agent preferably hydrogen peroxide, is used at least in the stoichiometrical ratio to the S ⁇ 2-charge in the off-gas before entering the second scrubber stage.
  • the S ⁇ 2-concentration in the clean gas after the second scrubber stage can be used as controlling parameter for the for the H2O2- dosage.
  • a further possibility of a controlled addition of oxidizing agent can also take place by a direct or indirect measurement of the concentration of oxidizing agents in the scrubber cycle of the second scrubber stage.
  • the molar ratio of the added amount of hydrogen peroxide in relation to the sulphur dioxide charge in the off-gas before entering the second scrubber stage is in the range of about 1 to 2, preferably about 1 to 1.5, in particular preferably about 1.2 to 1.3.
  • the sulphur dioxide is practically quantitatively separated under forming of sulphuric acid:
  • ammonia still left in the off-gas after the first scrubber stage is also separated in the second scrubber stage. To this purpose serves the sulphur acid resulting from the oxidation.
  • the result is a sulphuric acid ammonium sulphate solution.
  • the preferably slightly overstoichiometrical H 2 O 2 dosage in the ratio to SO 2 has the effect that the scrubber solution of the second scrubber stage may still contain low residual amounts of unspent H 2 O 2 .
  • the pH-value of the second scrubber stage is preferably between 1 und 5, more preferably between 2 und 4 and especially optimal at about 3.
  • the pH-value of this second scrubber stage is maintained by an appropriate cascade control of the variable desired pH-value of the first scrubber stage.
  • the mixture of sulphuric acid, ammonium sulphate and the unused oxidizing agent, for example hydrogen peroxide can preferably be fed back into the first scrubber stage.
  • the sulphuric acid present in relatively low amounts then reacts in the first scrubber stage with the added ammonia to ammonium sulphate.
  • the excess of also back fed hydrogen peroxide preferably oxidises still present ammonium sulfite to ammonium sulphate and thereby supports the oxidation process proceeding with the residual oxygen from the off-gas.
  • the sulphur dioxide is separated practically quantitatively.
  • the sulphuric acid formed in the second scrubber stage nearly completely absorbs the ammonia released in the preset stage.
  • extremely low clean gas concentrations of SO 2 and ammonia can be reached after the second scrubber stage.
  • Scrubber devices can be the described scrubber stages as empty spray absorption columns and/or scrubbers with scrubber water-impinged installations such as tower packings or sieve plates or nozzle plates, however also as bubble columns.
  • the operation of the individual stages can take place in co-, counter- or cross-current principle.
  • the individual scrubber stages are each provided in a preferable manner with droplet separators such as for example fibre packages, wet electro filters or inertia separators (for example cyclone separators).
  • the described scrubber stages can be replenished by further cleaning stages.
  • crude gas for example from a waste incinerator, can be cleared from fly ash by use of a respective filter.
  • tissue filters or electro filters can be preset before the two stage SO 2 -scrubber process so that the gas to be treated is released from fly ash or other dusts.
  • hydrochloric acid or hydrofluoric acid before entering the described two stage NH3/H 2 O 2 -scrubber process. So, by nozzling in of water into the hot smoke gas, a cooling down to saturation temperature can be effected.
  • the typical water vapour saturation temperature is about 60-65 0 C.
  • HgCI 2 important in the case of waste incineration
  • sulphur dioxide in the formed aqueous hydrochloric acid solution is regularly not separated.
  • hydrochloric acid and hydrofluoric acid can be reached for example by way of devices as for example with water-impinged tower packings, sieve bottom columns, but also with bubble columns or spray absorption columns which are each equipped with droplet separators.
  • the wet scrubber conduction of the scrubber process can be carried out as a method of direct current, counter current or cross current .
  • the crude gas 16 is cleared of fly ash 6 in the filter (a), (for example tissue filter or electro filter).
  • a cooling down of the off-gas to saturation temperature takes place by nozzling in of water 18.
  • the nozzling in of water 18 for the cooling of smoke gas can also be replaced or supplemented by scrubber water from scrubber stage b. In this case a common scrubber bottom of quench 17 and scrubber stage (b) is preferable.
  • a partial separation of HCI and hydrofluoric acid and also of HgCb takes place.
  • step (b) a nearly complete separation of hydrochloric acid and hydrofluoric acid is then carried out at pH-values of below 3, preferably 2 to 0.
  • the pH- value can be adjusted by the ratio of separated scrubber water to the entered HCI- charge and/or by controlled addition of a neutralization agent, for example NaOH or Ca(OH)2.
  • Both scrubber solutions of quench and stage (b) can have a common scrubber bottom.
  • a droplet separator 15 is used.
  • the device is equipped with a tower packing 14.
  • the scrubber water is led counter currently as cycle 20 to the off-gas through the tower packing 14.
  • the separated scrubber water 7 (aqueous hydrochloric acid and hydrofluoric acid solution and HgCb separated therein) and the vaporized water amount are replaced by fresh water 8 and/or 18 so that practically a constant volume of scrubber water in the water cycle is maintained.
  • the off-gas is then led via the pipe 9 into the first scrubber stage (c).
  • the variable desired pH-value is adjusted in the range of from 4 to 6.
  • the start-value of the desired pH-value of the first scrubber stage is achieved via a cascade controlling based on the pH-value (pH-value deviation) of the second scrubber stage (d).
  • the sulphur dioxide is separated mainly in form of ammonium sulphate and only in small amounts in the form of ammonium sulfite and separated as aqueous solution via the pipe 19.
  • a molar concentration ratio of sulphur dioxide to ammonia is adjusted in the off- gas 1 1 after the first scrubber stage.
  • the off-gas is then transferred via the pipe 11 into the second scrubber stage (d).
  • an aqueous hydrogen peroxide solution is added via pipe 12 into the water cycle 20.
  • the stoichiometrical ratio of hydrogen peroxide to sulphur dioxide is 1 ,3 in the example of the invention.
  • the pH- value in the second scrubber stage (d) is maintained at a value of between 2 and 4, preferably at a constant value of about 3.
  • the separation of sulphur dioxide and the release of NH3 are indirectly controlled.
  • a gas analysis (not shown) for the determination of the S ⁇ 2-concentration in the off-gas 11 before entry into the second scrubber stage (d) a controlling of the dosage of the hydrogen peroxide 12 into the second scrubber stage (d) takes place. Hydrogen peroxide is added in in an excess (stoichiometry in the range of 1 to 2) preferably 1.3.
  • the mixture of sulphuric acid and ammonium sulphate generated in the second scrubber stage (d) and unused hydrogen peroxide is fed back via pipe 5 into the first scrubber stage (c).
  • the cleaned off-gas is separated from the second scrubber stage (d) via pipe 13.
  • Figure 2 shows schematically the principal dependencies of the SO2- and IMH3- concentration in the off-gas from the pH-value after the first scrubber stage (c).
  • the SO2 concentration courses 1 and 2 in the off-gas after the first scrubber stage (c) depend on the pH-value of the first scrubber stage (c) and of the crude gas concentration.
  • Curve 1 shows by way of example the course of the SO2 clean gas concentration at low S ⁇ 2-crude gas concentration, and curve 2 at high crude gas concentration.
  • the release of NH3 depends essentially on the pH-value of the first scrubber stage.
  • the optimal operation point of the pH-value of the first scrubber stage is within the range of from about 4 to 6 in order to maintain a defined molar SO2/NH3 concentration ratio.
  • the desired-pH-value in the first scrubber stage (c) is adjusted in the range of 4-6 so that the result is a molar ratio of SO2 and NH3 in the off- gas in the range of 0.5 to 1 after the first scrubber stage (c).

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  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Environmental & Geological Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Biomedical Technology (AREA)
  • Analytical Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Treating Waste Gases (AREA)
  • Cleaning Or Drying Semiconductors (AREA)
PCT/EP2008/061013 2007-08-23 2008-08-22 Method for the cleaning of off-gas Ceased WO2009024612A1 (en)

Priority Applications (9)

Application Number Priority Date Filing Date Title
EP08827917.9A EP2180938B1 (en) 2007-08-23 2008-08-22 Method for the cleaning of off-gas
KR1020107006362A KR101535280B1 (ko) 2007-08-23 2008-08-22 오프-가스의 세정 방법
CN200880104087XA CN101842147B (zh) 2007-08-23 2008-08-22 净化尾气的方法
RU2010110637/05A RU2488431C2 (ru) 2007-08-23 2008-08-22 Способ очистки отходящих газов
JP2010521439A JP5455907B2 (ja) 2007-08-23 2008-08-22 排ガスの浄化法
CA2696199A CA2696199C (en) 2007-08-23 2008-08-22 Method for the cleaning of off-gas
DK08827917.9T DK2180938T3 (da) 2007-08-23 2008-08-22 Fremgangsmåde til rengøring af røggas
US12/733,314 US8048392B2 (en) 2007-08-23 2008-08-22 Method for the cleaning of off-gas
PL08827917T PL2180938T3 (pl) 2007-08-23 2008-08-22 Sposób oczyszczania gazu odlotowego

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102007039926.1 2007-08-23
DE102007039926A DE102007039926B4 (de) 2007-08-23 2007-08-23 Verfahren und Vorrichtung zur Abgasreinigung

Publications (1)

Publication Number Publication Date
WO2009024612A1 true WO2009024612A1 (en) 2009-02-26

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PCT/EP2008/061013 Ceased WO2009024612A1 (en) 2007-08-23 2008-08-22 Method for the cleaning of off-gas

Country Status (11)

Country Link
US (1) US8048392B2 (enExample)
EP (1) EP2180938B1 (enExample)
JP (1) JP5455907B2 (enExample)
KR (1) KR101535280B1 (enExample)
CN (1) CN101842147B (enExample)
CA (1) CA2696199C (enExample)
DE (1) DE102007039926B4 (enExample)
DK (1) DK2180938T3 (enExample)
PL (1) PL2180938T3 (enExample)
RU (1) RU2488431C2 (enExample)
WO (1) WO2009024612A1 (enExample)

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CN102205204B (zh) * 2011-06-02 2013-08-28 上海大学 冷热态出料的湿式氨法脱硫浓缩工艺
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