WO2011046491A1 - Additive to urea solutions - Google Patents

Additive to urea solutions Download PDF

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Publication number
WO2011046491A1
WO2011046491A1 PCT/SE2010/051057 SE2010051057W WO2011046491A1 WO 2011046491 A1 WO2011046491 A1 WO 2011046491A1 SE 2010051057 W SE2010051057 W SE 2010051057W WO 2011046491 A1 WO2011046491 A1 WO 2011046491A1
Authority
WO
WIPO (PCT)
Prior art keywords
urea
urea solution
additive
lumps
solution
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/SE2010/051057
Other languages
French (fr)
Inventor
Sara Sebelius
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.)
Dunas Dag
Original Assignee
Dunas Dag
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=43876348&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO2011046491(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Dunas Dag filed Critical Dunas Dag
Priority to CA2776509A priority Critical patent/CA2776509C/en
Priority to CN201080046532.9A priority patent/CN102665873B/en
Priority to BR112012008955A priority patent/BR112012008955A2/en
Priority to US13/501,114 priority patent/US20120219485A1/en
Priority to EP10823687.8A priority patent/EP2488283B1/en
Publication of WO2011046491A1 publication Critical patent/WO2011046491A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
    • F01N—GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL-COMBUSTION ENGINES
    • F01N3/00—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust
    • F01N3/08—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous
    • F01N3/10—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous by thermal or catalytic conversion of noxious components of exhaust
    • F01N3/18—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous by thermal or catalytic conversion of noxious components of exhaust characterised by methods of operation; Control
    • F01N3/20—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous by thermal or catalytic conversion of noxious components of exhaust characterised by methods of operation; Control specially adapted for catalytic conversion
    • 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
    • B01D53/54—Nitrogen compounds
    • B01D53/56—Nitrogen 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
    • B01D53/92—Chemical or biological purification of waste gases of engine exhaust gases
    • B01D53/94—Chemical or biological purification of waste gases of engine exhaust gases by catalytic processes
    • B01D53/9404—Removing only nitrogen compounds
    • B01D53/9409—Nitrogen oxides
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
    • F01N—GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL-COMBUSTION ENGINES
    • F01N3/00—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust
    • F01N3/08—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous
    • F01N3/10—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous by thermal or catalytic conversion of noxious components of exhaust
    • F01N3/18—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous by thermal or catalytic conversion of noxious components of exhaust characterised by methods of operation; Control
    • F01N3/20—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous by thermal or catalytic conversion of noxious components of exhaust characterised by methods of operation; Control specially adapted for catalytic conversion
    • F01N3/206—Adding periodically or continuously substances to exhaust gases for promoting purification, e.g. catalytic material in liquid form, NOx reducing agents
    • F01N3/2066—Selective catalytic reduction [SCR]
    • 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
    • B01D2251/2067—Urea
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2257/00—Components to be removed
    • B01D2257/40—Nitrogen compounds
    • B01D2257/404—Nitrogen oxides other than dinitrogen oxide
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D2258/00—Sources of waste gases
    • B01D2258/01—Engine exhaust gases
    • B01D2258/012—Diesel engines and lean burn gasoline engines
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
    • F01N—GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL-COMBUSTION ENGINES
    • F01N2570/00—Exhaust treating apparatus eliminating, absorbing or adsorbing specific elements or compounds
    • F01N2570/14—Nitrogen oxides
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
    • F01N—GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL-COMBUSTION ENGINES
    • F01N2610/00—Adding substances to exhaust gases
    • F01N2610/02—Adding substances to exhaust gases the substance being ammonia or urea
    • 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
    • Y02T—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
    • Y02T10/00—Road transport of goods or passengers
    • Y02T10/10—Internal combustion engine [ICE] based vehicles
    • Y02T10/12—Improving ICE efficiencies

Definitions

  • This invention concerns the use of compounds within the class of compounds
  • SCR Selective Catalytic Reduction
  • the reducing agent a 32.5 percent aqueous solution of urea that is kept in a tank connected to the catalytic converter, is injected before the catalytic converter and is subsequently split into ammonia in the catalytic converter.
  • Ammonia reacts with the nitrogen oxides as follows:
  • urea may be transformed into various other products that form hard deposits and lumps which might clog or break the catalytic converter.
  • additives designed to prevent the formation of lumps.
  • These additives are not mixable with the urea solution at room temperature, and therefore a preliminary mixing of the additive and the urea must be done in a factory.
  • the additives currently on the market decompose into products that cause deposits which are difficult to dissolve.
  • the additive in accordance with the invention is mixable with the urea solution at room temperature and does not decompose into products that may cause deposits.
  • Urea solution 1 was composed of a 32.5 percent aqueous solution of urea (the largest commercial available brand on the market).
  • Urea solution 2 was composed of a 32.5 percent aqueous solution of urea (another commercial available brand on the market).
  • Urea solution 3 was composed of the 32.5 percent aqueous solution of urea that is sold premixed with an additive (Diaxol ® ).
  • Urea solution 4 was composed of urea solution 1 with ⁇ 0.1% of an additive of the class C x+ iH 2x +3(C 2 H 4 0) y OH. The mixing was done at room temperature.
  • Urea solution 5 was composed of urea solution 2 with ⁇ 0.1% of an additive of the class C x+ iH 2X +3(C 2 H 4 0) y OH. The mixing was done at room temperature.
  • the urea solution was injected in a system of 250°C and 350°C (common exhaust temperatures for lump formation). All experiments were repeated twice.

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Combustion & Propulsion (AREA)
  • General Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Toxicology (AREA)
  • Biomedical Technology (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • General Chemical & Material Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Environmental & Geological Engineering (AREA)
  • Exhaust Gas After Treatment (AREA)
  • Exhaust Gas Treatment By Means Of Catalyst (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Heat Sensitive Colour Forming Recording (AREA)

Abstract

Use of compounds from the class of compounds Cx+1H2X+3(C2H4O)yOH where x = (44y/ W - 44y + 17/ W - 32) / 14 x ≥ 0 1 ≤y≤20 0.58 ≤ W ≤ 1.0 as additive to urea solutions to counteract the risk of clogging of catalytic converters.

Description

ADDITIVE TO UREA SOLUTIONS
Description Technological Area
This invention concerns the use of compounds within the class of compounds
Cx+iH2x+3(C2H40)yOH as additive to urea solutions for catalytic converters.
The Standpoint of Technology
The predominant exhaust after-treatment technique for diesel engines on the market today is the Selective Catalytic Reduction (SCR). In SCR technology, the poisonous nitrogen oxides formed in the engine combustion are transformed into molecular nitrogen and water by reduction. The reducing agent, a 32.5 percent aqueous solution of urea that is kept in a tank connected to the catalytic converter, is injected before the catalytic converter and is subsequently split into ammonia in the catalytic converter. Ammonia reacts with the nitrogen oxides as follows:
NOx + NH3→ N2 + H20
However, this technology is not problem-free. Instead of forming ammonia, urea may be transformed into various other products that form hard deposits and lumps which might clog or break the catalytic converter. On the market there are already additives designed to prevent the formation of lumps. These additives, however, are not mixable with the urea solution at room temperature, and therefore a preliminary mixing of the additive and the urea must be done in a factory. Furthermore, the additives currently on the market decompose into products that cause deposits which are difficult to dissolve. The additive in accordance with the invention is mixable with the urea solution at room temperature and does not decompose into products that may cause deposits.
The Solution of the Problem
The invention at hand solves the problems of the known technique in accordance with the distinctive features stated in the following request for a patent. A Detailed Description of the Invention
We have discovered that the class of compounds that we define below accelerates the transition from urea into ammonia, thus counteracting the risk of formation of lumps. Laboratory experiments have shown that the addition of only a small amount (<0.1%) of a compound out of this class of compounds to the urea solution nearly eliminates the risk of deposits and the formation of lumps in the catalytic converter. The compounds in this class of compounds are possible to mix with the urea solution at room temperature. This means that the premixing of the additive and the urea solution does not have to be done in a factory but that the additive can be poured directly into the tank where the urea solution is filled. The class of compounds has no negative impact on the environment and neither does it decompose into compounds that might damage the environment or the catalytic converters.
The application for a patent concerns the use of the following class of compounds as additive to urea solutions with the purpose of minimizing deposits and the formations of lumps in the SCR system:
H2x+3(C2H40)yOH where x = I (44y/W - 44y + 17/W - 32) / 14 x > 0 1 < y < 20
0.58 < W < 1.0
Experimental Part
Urea solution 1 was composed of a 32.5 percent aqueous solution of urea (the largest commercial available brand on the market).
Urea solution 2 was composed of a 32.5 percent aqueous solution of urea (another commercial available brand on the market).
Urea solution 3 was composed of the 32.5 percent aqueous solution of urea that is sold premixed with an additive (Diaxol®). Urea solution 4 was composed of urea solution 1 with <0.1% of an additive of the class Cx+iH2x+3(C2H40)yOH. The mixing was done at room temperature.
Urea solution 5 was composed of urea solution 2 with <0.1% of an additive of the class Cx+iH2X+3(C2H40)yOH. The mixing was done at room temperature.
The urea solution was injected in a system of 250°C and 350°C (common exhaust temperatures for lump formation). All experiments were repeated twice.
Experiment A
After sixteen hours at 250°C white lumps the size of a decimetre had formed in both the experiments with urea solution 1 and urea solution 2, whereas the experiments with urea solution 3, urea solution 4 and urea solution 5 caused hardly any white deposits. With urea solution 3 insoluble black deposits had formed. Both inorganic and organic solvents were tested. No black deposits were observed for urea solution 4 and urea solution 5.
Experiment B
After sixteen hours at 350°C white lumps the size of a centimetre had formed in both the experiments with urea solution 1 and urea solution 2, whereas the experiments with urea solution 3, urea solution 4 and urea solution 5 caused no white deposits at all.
With urea solution 3 insoluble black deposits had formed. The black deposits had begun to form as early as after half an hour. No black deposits were observed for urea solution 4 and urea solution 5. The ability to reduce the formation of lumps of urea and its decomposition products (the white lumps) was consequently as good for urea solution 4 and urea solution 5 as for urea solution 3. Unique for urea solution 4 and urea solution 5 (urea solutions with additive Cx+iH2X+3(C2H40)yOH) was that they (unlike urea solution 3) caused no insoluble black deposits.
We observe the same effect for additives from the class of componds
Cx+iH2X+3(C2H40)yOH when y varies between 1 and 20. Neither C3H7(C2H40)iOH, C6Hi3(C2H40)4OH, C9Hi9(C2H40)ioOH nor Ci8H37(C2H4O)20OH caused any black deposits, and the white lumps of urea had nearly been eliminated in both experiment A and experiment B. Comparative experiments have also been carried out with the previously known additives diethylene glycol and polyethylene glycol which show that they do not achieve as high an effect in reducing the formation of white lumps. See below. When H(C2H40)2OH (diethylene glycol) and H(C2H4O)i0OH (polyethylene glycol) are used as additives, urea lumps are formed to a lesser extent than in the experiments without an additive (urea solution 1 and urea solution 2), but the ability to reduce the formation of lumps is not as high as the ability of the additives Cx+iH2x+3(C2H40)yOH. When diethylene glycol or polyethylene glycol is used as an additive to urea solution 1 and urea solution 2 and is injected during sixteen hours at 250°C (compare experiment A) white urea lumps are formed that are a third of the size compared to the urea solutions without an additive. At an injection of sixteen hours at 350°C (compare experiment B) white urea lumps are formed half the size compared to the urea solutions without an additive. The formation of lumps is accordingly reduced, but not at all to as high an extent as with additives from the class of compounds Cx+iH2x+3(C2H40)yOH.
We have also within our class of compunds been able to observe the importance of the length of the carbon chain of the additive. A shorter carbon chain gives an inferior effect to counteract the formation of urea lumps. CH3(C2H40)OH causes a little more white deposits than C3H7(C2H40)OH. In the same way CH3(C2H40)2OH shows somewhat inferior qualities to C4H9(C2H40)2OH, but both CH3(C2H40)2OH and C4H9(C2H40)2OH show a better reducing ability toward the formation of white urea lumps than their corresponding ethylene glycols without a carbon chain (diethylene glycol).

Claims

Claim
l .Use of the class of compounds Cx+iH2x+3(C2H40)yOH
where
x = I (44y/W - 44y + 17/W - 32) / 14 | x > 0
1 < y < 20
0.58 < W < 1.0
as additive to urea solutions for catalytic converters in exhaust after-treatment.
PCT/SE2010/051057 2009-10-16 2010-10-01 Additive to urea solutions Ceased WO2011046491A1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
CA2776509A CA2776509C (en) 2009-10-16 2010-10-01 Additive to urea solutions
CN201080046532.9A CN102665873B (en) 2009-10-16 2010-10-01 Additive to urea solutions
BR112012008955A BR112012008955A2 (en) 2009-10-16 2010-10-01 additive for urea solutions
US13/501,114 US20120219485A1 (en) 2009-10-16 2010-10-01 Additive to urea solutions
EP10823687.8A EP2488283B1 (en) 2009-10-16 2010-10-01 Additive to urea solutions

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
SE0901329 2009-10-16
SE0901329-3 2009-10-16
SE1000404-2 2010-04-21
SE1000404A SE534217E (en) 2009-10-16 2010-04-21 Substance to add urea solutions

Publications (1)

Publication Number Publication Date
WO2011046491A1 true WO2011046491A1 (en) 2011-04-21

Family

ID=43876348

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/SE2010/051057 Ceased WO2011046491A1 (en) 2009-10-16 2010-10-01 Additive to urea solutions

Country Status (7)

Country Link
US (1) US20120219485A1 (en)
EP (1) EP2488283B1 (en)
CN (1) CN102665873B (en)
BR (1) BR112012008955A2 (en)
CA (1) CA2776509C (en)
SE (1) SE534217E (en)
WO (1) WO2011046491A1 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10399035B2 (en) 2015-12-02 2019-09-03 Total Marketing Services Composition made from urea for treating exhaust gases
EP4122584A1 (en) 2021-07-23 2023-01-25 Basf Se Reductant fluid for the after-treatment of exhaust gas
WO2023118397A1 (en) 2021-12-22 2023-06-29 Xenum Nv/Sa Additive for nox reducing solution
PL243193B1 (en) * 2020-12-30 2023-07-17 Storage Partners Spolka Z Ograniczona Odpowiedzialnoscia Spolka Komandytowa A method of producing a preparation supporting the cleaning of exhaust gases from nitrogen oxides, especially exhaust gases emitted by diesel engines

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Publication number Priority date Publication date Assignee Title
JP5906637B2 (en) * 2011-09-28 2016-04-20 いすゞ自動車株式会社 Foreign matter removal method and selective reduction catalyst system
CN104226093A (en) * 2014-07-17 2014-12-24 赵根华 Composite additive of automobile urea solution
FR3064495B1 (en) 2017-03-31 2021-04-02 Total Marketing Services UREA-BASED COMPOSITION FOR THE TREATMENT OF EXHAUST GASES
WO2020047653A1 (en) 2018-09-05 2020-03-12 WEnTech Solutions Inc. System and method for anaerobic digestion process assessment, optimization and/or control
FR3108529A1 (en) 2020-03-30 2021-10-01 Total Marketing Services Use of a composition comprising a reducing agent, at least one paraffin and a metal compound to prevent deposits in the exhaust lines comprising an SCR catalyst
FR3108527B1 (en) 2020-03-30 2022-09-09 Total Marketing Services Use of a composition comprising a reducing agent and a metal compound to prevent deposits in exhaust lines comprising an SCR catalyst
FR3108526B1 (en) 2020-03-30 2022-09-09 Total Marketing Services Use of a composition comprising a reducing agent, a surfactant and a metal compound to prevent deposits in exhaust lines comprising an SCR catalyst
FR3124598A1 (en) 2021-06-25 2022-12-30 Total Marketing Services Method for detecting the presence of an additive in an exhaust gas treatment composition
EP4115970A1 (en) 2021-07-05 2023-01-11 TUNAP GmbH & Co. KG Additive for cleaning scr systems
FR3125535B1 (en) 2021-07-23 2023-07-28 Totalenergies Marketing Services Aqueous composition for the treatment of exhaust gases with improved antifoam properties
FR3138048A1 (en) 2022-07-19 2024-01-26 Totalenergies Onetech Aqueous composition for exhaust gas treatment with improved properties
CN119768221A (en) 2022-08-30 2025-04-04 道达尔能源一技术 Aqueous compositions with improved properties for treating exhaust gases
KR20250157002A (en) 2024-04-26 2025-11-04 김송기 DEF additive composition for vehicles, DEF solution comprising the same, and a method of making the same

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US20040115110A1 (en) * 2001-11-06 2004-06-17 Wolfgang Ripper Method and device for reducing nitrogen oxides present in exhaust gas
CA2679088A1 (en) * 2007-02-23 2008-10-23 Total Raffinage Marketing Aqueous solution for the treatment of exhaust gases of diesel engines

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US20040115110A1 (en) * 2001-11-06 2004-06-17 Wolfgang Ripper Method and device for reducing nitrogen oxides present in exhaust gas
CA2679088A1 (en) * 2007-02-23 2008-10-23 Total Raffinage Marketing Aqueous solution for the treatment of exhaust gases of diesel engines

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Title
See also references of EP2488283A4 *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10399035B2 (en) 2015-12-02 2019-09-03 Total Marketing Services Composition made from urea for treating exhaust gases
PL243193B1 (en) * 2020-12-30 2023-07-17 Storage Partners Spolka Z Ograniczona Odpowiedzialnoscia Spolka Komandytowa A method of producing a preparation supporting the cleaning of exhaust gases from nitrogen oxides, especially exhaust gases emitted by diesel engines
EP4122584A1 (en) 2021-07-23 2023-01-25 Basf Se Reductant fluid for the after-treatment of exhaust gas
WO2023118397A1 (en) 2021-12-22 2023-06-29 Xenum Nv/Sa Additive for nox reducing solution

Also Published As

Publication number Publication date
CA2776509C (en) 2017-06-06
CA2776509A1 (en) 2011-04-21
US20120219485A1 (en) 2012-08-30
EP2488283B1 (en) 2014-12-24
CN102665873A (en) 2012-09-12
SE534217E (en) 2015-06-23
SE534217C2 (en) 2011-06-07
BR112012008955A2 (en) 2018-11-06
SE1000404A1 (en) 2011-04-17
EP2488283A1 (en) 2012-08-22
EP2488283A4 (en) 2013-10-30
CN102665873B (en) 2014-12-03

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