EP2414106A1 - Revêtement sans chrome pour un substrat - Google Patents

Revêtement sans chrome pour un substrat

Info

Publication number
EP2414106A1
EP2414106A1 EP10756469A EP10756469A EP2414106A1 EP 2414106 A1 EP2414106 A1 EP 2414106A1 EP 10756469 A EP10756469 A EP 10756469A EP 10756469 A EP10756469 A EP 10756469A EP 2414106 A1 EP2414106 A1 EP 2414106A1
Authority
EP
European Patent Office
Prior art keywords
weight
range
aluminum
silicon
nickel
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP10756469A
Other languages
German (de)
English (en)
Other versions
EP2414106B1 (fr
EP2414106A4 (fr
Inventor
Michael W. Seitz
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.)
General Electric Technology GmbH
Original Assignee
Alstom Technology AG
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 Alstom Technology AG filed Critical Alstom Technology AG
Priority to PL10756469T priority Critical patent/PL2414106T3/pl
Publication of EP2414106A1 publication Critical patent/EP2414106A1/fr
Publication of EP2414106A4 publication Critical patent/EP2414106A4/fr
Application granted granted Critical
Publication of EP2414106B1 publication Critical patent/EP2414106B1/fr
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C30/00Coating with metallic material characterised only by the composition of the metallic material, i.e. not characterised by the coating process
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C4/00Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
    • C23C4/04Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
    • C23C4/06Metallic material
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C4/00Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
    • C23C4/04Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
    • C23C4/06Metallic material
    • C23C4/067Metallic material containing free particles of non-metal elements, e.g. carbon, silicon, boron, phosphorus or arsenic
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C4/00Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
    • C23C4/12Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the method of spraying
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C4/00Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
    • C23C4/12Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the method of spraying
    • C23C4/131Wire arc spraying

Definitions

  • This invention relates to chrome-free metal coating compositions and thermal spray wires for producing same.
  • a composite of precursor materials for forming a chromium-free metallic coating In one embodiment of the invention, there is provided a composite of precursor materials for forming a chromium-free metallic coating. In another embodiment of the invention, the precursor materials are provided in the form of a composite wire. In a further embodiment of the invention, there is provided a chromium-free metallic coating as can be made from the wire.
  • the chromium-free metallic coating precursor comprises a base metal constituent, a silicon constituent, a titanium constituent, and a boron constituent.
  • the base metal constituent is present in amount of at least about 54% by weight.
  • the base metal constituent comprises at least one base metal selected the group consisting of iron, nickel, cobalt, lead, zinc, copper, tin, and aluminum and always comprises at least about 1% by weight of alloyed aluminum and/or silicon, based on mass of the coating precursor.
  • the silicon, titanium and boron constituents are each present in amount between about 1% and about 15% by weight.
  • the above constituents can be provided in a composite wire in accordance with another embodiment of the invention.
  • the composite wire usually comprises a metallic outer sheath in the range of 70 to 95% by weight and an inner core in the range of about 5 to about 30% by weight.
  • the metallic outer sheath preferably comprises at least about 70 weight percent of a base metal readily capable of being rolled and drawn into the sheath and at least about 2 weight percent alloyed aluminum and/or silicon.
  • the inner core in one embodiment of the invention comprises in the range of about 15% to about 30% titanium, in the range of about 15% to about 35% silicon, in the range of about 20% to about 50% boron, and in the range of 0% to 15% carbon, all preferably in particle form.
  • the composite wire can be applied by thermal spray technique to produce the metallic chrome-free coating of the invention on a substrate.
  • the chrome-free coating composition usually comprises, in bulk on a weight basis, about 60 to about 90% of base metal, at least about 2% aluminum, about 2 to about 10% titanium, about 2 to about 10% silicon, and about 2 to about 10% boron.
  • the coating is high temperature wear and corrosion resistant.
  • the drawing illustrates pictorially a composite wire in accordance with an embodiment of the invention.
  • the chromium-free metallic coating precursor comprises a base metal constituent, a silicon constituent, a titanium constituent, and a boron constituent, in alloy, mixture or composite form.
  • the base metal constituent is present in amount of at least about 54% by weight.
  • the base metal constituent usually comprises at least one base metal selected the group consisting of iron, nickel, cobalt, lead, zinc, copper, tin, and aluminum and always comprises at least about 1% by weight of alloyed aluminum and/or silicon, based on mass of the coating precursor.
  • the silicon, titanium and boron constituents are each present in amount between about 1% and about 15% by weight.
  • the base metal is present in an amount of at least about 68% by weight and contains an aluminum and/or silicon component alloyed therein in an amount of at least about 2% by weight, based on mass of coating precursor.
  • the silicon, titanium and boron are each present in amount between about 2% and 10 percent by weight.
  • the base metal constituent is present in an amount of at least about 76% by weight and is selected from at least one of iron, nickel, cobalt, and aluminum.
  • the base metal constituent is a mixture or an alloy, preferably an alloy, and always comprises at least about 3% by weight of aluminum, based on mass of coating precursor.
  • the silicon, titanium and boron are present, preferably as a mass in particle form, in amount between about 4% and about 7%, preferably as the inside of a composite wire formed from the base metal constituent.
  • the coatings of the present invention can be formed from composite wires as described herein by feeding the wires through a conventional arc spraying apparatus.
  • the composite wire 10 comprises a metallic outer sheath 20 in the range of 70 to 95% by weight and an inner core 30 in the range of about 5 to about 30% by weight.
  • the composite wire comprises a metallic outer sheath in the range of about 75 to about 85% by weight and an inner core in the range of about 15 to about 25% by weight.
  • the metallic outer sheath preferably comprises at least about 70 weight percent of a base metal readily capable of being rolled and drawn into the sheath and at least about 2 weight percent alloyed aluminum and/or silicon. Aluminum can also be employed exclusively as the base metal.
  • the inner core in one embodiment of the invention comprises in the range of about 15% to about 30% titanium, in the range of about 15% to about 35% silicon, in the range of about 20% to about 50% boron, and in the range of 0% to 15% carbon, all preferably in particle, preferably powdered, mixture form.
  • the titanium, silicon and boron may be present as a mixture of compounds containing additional elements.
  • the base metal is preferably a relatively soft elemental metal or alloy, for example, at least one of nickel, iron, or cobalt.
  • Nickel is preferred, and the outer sheath most preferably comprises an alloy of nickel and aluminum.
  • Exemplary materials comprise in the range of about 70 to about 98 percent by weight of nickel and in the range of about 2 to about 30 percent by weight of alloyed aluminum and/or silicon, preferably in the range of about 85 to about 98 percent by weight of nickel and in the range of about 2 to about 15 percent by weight alloyed aluminum and/or silicon, and most preferably about 90 to about 97 percent by weight of nickel and in the range of about 3 to about 10 percent by weight of alloyed aluminum.
  • the inner core preferably comprises in the range of about 20% to about 30% titanium, in the range of about 20% to about 30% silicon, in the range of about 30% to about 40% boron, and in the range of 0% to about 15% carbon.
  • Carbon generally in the form of carbides, can be present if desired in the inner core, but since it is probably not present in the coating composition, at least in amounts which contribute properties, it is not considered material to the coating invention.
  • the titanium and silicon can be provided by a suitable amount of a TiSi source, for example, in the range of about 50 to about 60% of a TiSi source such as TiSiFe in admixture with a source of boron and optional carbon, for example, B 4 C in an amount of about 40 to about 50%.
  • the inner core may also contain additional materials.
  • the additional materials may include: carbides, such as tungsten carbide, titanium carbide, vanadium carbide, and the like; oxides, such as aluminum oxide, zirconium oxide, and the like; and borides, such as nickel boride, iron boride, and the like.
  • the inner core may also include additional metal powders, such as aluminum, nickel, or alloy powder, or composite powders, such as tungsten carbide nickel.
  • the inner core can include in the range of about 0. 1 to about 10% molybdenum, about 0. 1 to about 10% tungsten, about 0.1 to about 10% neodymium, and about 0. 1 to about 10% carbon.
  • metal or metal alloy powders comprising magnesium, phosphorus, vanadium, manganese, iron, cobalt, nickel, copper, zirconium, niobium, molybdenum, tantalum and/or tungsten may be present in the inner core, for example, in the range of about 0. 1 to about 10%.
  • the core components listed above can be alloyed into the sheath, and where this is done, the constituent need not be present in the inner core, or it can be present in a reduced amount.
  • titanium, silicon and boron can be alloyed in the sheath in the amount of about 2 to about 10% by weight, based on weight of the composite wire.
  • the aluminum component may be present in the inner core, rather than the sheath.
  • the grain size of the powdered inner core will have an effect on the physical properties of the applied coating. Generally, the finer the grains of the powder, the more homogenous the coating will be and generally the better the wear and corrosion properties. However, acquisition costs and manufacturing constraints will limit the lower end of the grain size range.
  • the cored wires may be formed in a conventional manner by placing the mix for forming the inner core, which need not be an agglomerated mix, onto the strip to be made into the outer metallic sheath. The strip can be drawn continuously through a plurality of wire drawing dies to form an outer wire sheath around an inner core.
  • the final outer diameter of the cored wire will depend upon the application for which it is used. For most applications, the cored wire final diameter ranges between about 0.8 mm and about 6.4 mm.
  • Conventional cored wire manufacturing techniques are disclosed in U. S. Patent Nos. 6, 156,443 (Dallaire et al.) and 6,513 ,728 (Hughes et al.), both being hereby incorporated by reference.
  • a method of forming a wear resistant and corrosion resistant coating on a substrate is also provided.
  • the method generally includes the steps of providing a composite wire having an outer sheath formed from a metal or alloy, and a powdered inner core, and coating a substrate by employing the composite wire in conjunction with thermal spraying techniques to form a fused metallic coating.
  • the inventive wire is not weldable by commonly available techniques, so non-welding methods must be used to form the fused coating.
  • the resulting fused metallic chrome-free coating composition usually comprises, in bulk on a weight basis, about 60 to about 90% of base metal, at least about 2% aluminum, about 2 to about 10% titanium, about 2 to about 10% silicon, and about 2 to about 10% boron.
  • the base metal is preferably selected from the group consisting of at least one of nickel, iron and cobalt, most preferably nickel.
  • the coating can contain additional constituents if desired, for example, additional constituents selected from the group consisting of about 0. 1 to about
  • the coatings according to the present invention are specifically designed for articles subjected to wear and/or corrosion.
  • Such articles include, for example, boiler tubes, hydraulic piston rods, pump casings, rollers in the paper and steel industry, wear plates, journals and shafts, and turbine blades and casings.
  • the coatings are designed to protect boiler tubes against erosion-corrosion related wastage and are applied to the boiler tubes by means of a conventional arc spraying apparatus.
  • arc spraying apparatus employing wires as the feed material.
  • Arc spraying methods and apparatus are well documented in the art, see for example, U. S. Pat. Nos. 6, 156,443 (Dallaire, et al.); 5,837,326 (Dallaire, et al.); and European Patent No. EP 0 522 438 (Zurecki et al.) the disclosures of which are incorporated by reference.
  • a composite wire was formed according to the following composition.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Plasma & Fusion (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Coating By Spraying Or Casting (AREA)
  • Nonmetallic Welding Materials (AREA)
  • Other Surface Treatments For Metallic Materials (AREA)

Abstract

L'invention porte sur un mélange ou alliage sans chrome, de préférence un fil métallique composite, pour la production d'un revêtement résistant à l'usure et résistant à la corrosion sur un substrat, par exemple par des techniques de projection à chaud. Les propriétés physiques du revêtement sont particulièrement appropriées pour des environnements d'érosion-corrosion à haute température. Le revêtement ainsi obtenu présente une bonne dureté, une bonne ténacité et de bonnes caractéristiques de collage. Le fil métallique composite comprend une gaine externe métallique et une âme interne et produit un revêtement sans chrome comprenant, en gros sur une base pondérale, 60 à 90 % d'un métal de base comprenant au moins 2 % d'aluminium et/ou de silicium, 2 à 10 % de titane, 2 à 10 % de silicium et 2 à 10 % de bore.
EP10756469.2A 2009-03-24 2010-03-24 Revêtement sans chrome, procédé de sa production et câble composite Active EP2414106B1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PL10756469T PL2414106T3 (pl) 2009-03-24 2010-03-24 Bezchromowa powłoka metaliczna, sposób formowania takiej powłoki i drutu kompozytowego

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US21090309P 2009-03-24 2009-03-24
PCT/US2010/000858 WO2010110873A1 (fr) 2009-03-24 2010-03-24 Revêtement sans chrome pour un substrat

Publications (3)

Publication Number Publication Date
EP2414106A1 true EP2414106A1 (fr) 2012-02-08
EP2414106A4 EP2414106A4 (fr) 2014-05-14
EP2414106B1 EP2414106B1 (fr) 2020-12-30

Family

ID=42781327

Family Applications (1)

Application Number Title Priority Date Filing Date
EP10756469.2A Active EP2414106B1 (fr) 2009-03-24 2010-03-24 Revêtement sans chrome, procédé de sa production et câble composite

Country Status (9)

Country Link
EP (1) EP2414106B1 (fr)
JP (1) JP5275509B2 (fr)
KR (1) KR101548553B1 (fr)
CN (1) CN102387870B (fr)
AU (1) AU2010229319B2 (fr)
CA (1) CA2756033C (fr)
MX (1) MX2011009089A (fr)
PL (1) PL2414106T3 (fr)
WO (1) WO2010110873A1 (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9475154B2 (en) 2013-05-30 2016-10-25 Lincoln Global, Inc. High boron hardfacing electrode
CN109989999A (zh) * 2017-12-29 2019-07-09 圣戈班性能塑料帕姆普斯有限公司 轴承部件及其制备和使用方法

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH311869A (de) * 1951-08-06 1955-12-15 Deutsche Edelstahlwerke Ag Verfahren zur Herstellung einer Dauermagnetlegierung.
GB2250030A (en) * 1990-11-22 1992-05-27 Castolin Sa Flux-cored wire containing elements and/or metallic hard substances; spraying; welding
DE4328732C1 (de) * 1993-08-26 1995-02-16 Castolin Sa Verfahren zum Herstellen einer thermisch gespritzten metallhaltigen Schicht sowie Werkstoff dafür
DE10259141A1 (de) * 2002-12-18 2004-07-08 Corodur Verschleiss-Schutz Gmbh Werkstoffsystem zum thermischen Beschichten
US20060078749A1 (en) * 2003-02-19 2006-04-13 Stefan Grau Composite material consisting of intermetallic phases and ceramics and production method for said material
US20080098926A1 (en) * 2003-06-06 2008-05-01 Michael Seitz Composite wires for coating substrates and methods of use
US20090032501A1 (en) * 2005-08-12 2009-02-05 Deloro Stellite Holdings Corporation Abrasion-resistant weld overlay

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4039318A (en) * 1976-07-19 1977-08-02 Eutectic Corporation Metaliferous flame spray material for producing machinable coatings
US4741974A (en) * 1986-05-20 1988-05-03 The Perkin-Elmer Corporation Composite wire for wear resistant coatings
AU6390790A (en) * 1989-10-30 1991-05-02 Lanxide Corporation Anti-ballistic materials and methods of making the same
US6156443A (en) 1998-03-24 2000-12-05 National Research Council Of Canada Method of producing improved erosion resistant coatings and the coatings produced thereby
US6258185B1 (en) * 1999-05-25 2001-07-10 Bechtel Bwxt Idaho, Llc Methods of forming steel
DE10036262B4 (de) * 2000-07-26 2004-09-16 Daimlerchrysler Ag Verfahren zur Herstellung einer Oberflächenschicht und Oberflächenschicht
US6513728B1 (en) 2000-11-13 2003-02-04 Concept Alloys, L.L.C. Thermal spray apparatus and method having a wire electrode with core of multiplex composite powder its method of manufacture and use
US7482061B2 (en) * 2004-11-30 2009-01-27 Momentive Performance Materials Inc. Chromium free corrosion resistant surface treatments using siliconized barrier coatings
FR2886182B1 (fr) * 2005-05-26 2009-01-30 Snecma Services Sa Poudre de superalliage

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH311869A (de) * 1951-08-06 1955-12-15 Deutsche Edelstahlwerke Ag Verfahren zur Herstellung einer Dauermagnetlegierung.
GB2250030A (en) * 1990-11-22 1992-05-27 Castolin Sa Flux-cored wire containing elements and/or metallic hard substances; spraying; welding
DE4328732C1 (de) * 1993-08-26 1995-02-16 Castolin Sa Verfahren zum Herstellen einer thermisch gespritzten metallhaltigen Schicht sowie Werkstoff dafür
DE10259141A1 (de) * 2002-12-18 2004-07-08 Corodur Verschleiss-Schutz Gmbh Werkstoffsystem zum thermischen Beschichten
US20060078749A1 (en) * 2003-02-19 2006-04-13 Stefan Grau Composite material consisting of intermetallic phases and ceramics and production method for said material
US20080098926A1 (en) * 2003-06-06 2008-05-01 Michael Seitz Composite wires for coating substrates and methods of use
US20090032501A1 (en) * 2005-08-12 2009-02-05 Deloro Stellite Holdings Corporation Abrasion-resistant weld overlay

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of WO2010110873A1 *

Also Published As

Publication number Publication date
AU2010229319A1 (en) 2011-10-13
AU2010229319B2 (en) 2015-09-17
KR101548553B1 (ko) 2015-09-01
CN102387870A (zh) 2012-03-21
PL2414106T3 (pl) 2021-05-31
MX2011009089A (es) 2011-09-27
CA2756033A1 (fr) 2010-09-30
JP2012521496A (ja) 2012-09-13
CN102387870B (zh) 2015-05-20
WO2010110873A1 (fr) 2010-09-30
CA2756033C (fr) 2014-01-28
EP2414106B1 (fr) 2020-12-30
KR20120009422A (ko) 2012-02-01
JP5275509B2 (ja) 2013-08-28
EP2414106A4 (fr) 2014-05-14

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