EP0576366B1 - Revêtements métalliques à base d'alliages amorphes résistant à l'usure et à la corrosion, procédé d'obtention et applications aux revêtements anti-usure pour matériel hydraulique - Google Patents
Revêtements métalliques à base d'alliages amorphes résistant à l'usure et à la corrosion, procédé d'obtention et applications aux revêtements anti-usure pour matériel hydraulique Download PDFInfo
- Publication number
- EP0576366B1 EP0576366B1 EP93420202A EP93420202A EP0576366B1 EP 0576366 B1 EP0576366 B1 EP 0576366B1 EP 93420202 A EP93420202 A EP 93420202A EP 93420202 A EP93420202 A EP 93420202A EP 0576366 B1 EP0576366 B1 EP 0576366B1
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- EP
- European Patent Office
- Prior art keywords
- resistant
- wear
- corrosion
- alloys
- amorphous metal
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- 230000007797 corrosion Effects 0.000 title claims abstract description 32
- 238000005260 corrosion Methods 0.000 title claims abstract description 32
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- 238000000034 method Methods 0.000 title claims description 20
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- 239000000956 alloy Substances 0.000 title abstract description 53
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- 239000000843 powder Substances 0.000 claims abstract description 15
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- 229910001092 metal group alloy Inorganic materials 0.000 claims abstract description 10
- 229910052759 nickel Inorganic materials 0.000 claims abstract description 10
- 229910052752 metalloid Inorganic materials 0.000 claims abstract description 8
- 150000002738 metalloids Chemical class 0.000 claims abstract description 7
- 229910052802 copper Inorganic materials 0.000 claims abstract description 6
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- 238000012360 testing method Methods 0.000 description 4
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 3
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- 239000000470 constituent Substances 0.000 description 3
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- 229910000975 Carbon steel Inorganic materials 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 101000928670 Homo sapiens Amyloid beta precursor protein binding family B member 1 Proteins 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 229910001347 Stellite Inorganic materials 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
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- 239000010962 carbon steel Substances 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- AHICWQREWHDHHF-UHFFFAOYSA-N chromium;cobalt;iron;manganese;methane;molybdenum;nickel;silicon;tungsten Chemical compound C.[Si].[Cr].[Mn].[Fe].[Co].[Ni].[Mo].[W] AHICWQREWHDHHF-UHFFFAOYSA-N 0.000 description 2
- 230000008094 contradictory effect Effects 0.000 description 2
- QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 description 2
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- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229910000746 Structural steel Inorganic materials 0.000 description 1
- HIGRAKVNKLCVCA-UHFFFAOYSA-N alumine Chemical compound C1=CC=[Al]C=C1 HIGRAKVNKLCVCA-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
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- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
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- 239000010419 fine particle Substances 0.000 description 1
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- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
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- OANVFVBYPNXRLD-UHFFFAOYSA-M propyromazine bromide Chemical compound [Br-].C12=CC=CC=C2SC2=CC=CC=C2N1C(=O)C(C)[N+]1(C)CCCC1 OANVFVBYPNXRLD-UHFFFAOYSA-M 0.000 description 1
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- 238000005480 shot peening Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
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- 239000000243 solution Substances 0.000 description 1
- 238000009718 spray deposition Methods 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
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- C—CHEMISTRY; METALLURGY
- C23—COATING 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
- C23C—COATING 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
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/04—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
- C23C4/06—Metallic material
- C23C4/08—Metallic material containing only metal elements
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C45/00—Amorphous alloys
- C22C45/008—Amorphous alloys with Fe, Co or Ni as the major constituent
-
- C—CHEMISTRY; METALLURGY
- C23—COATING 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
- C23C—COATING 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
- C23C30/00—Coating with metallic material characterised only by the composition of the metallic material, i.e. not characterised by the coating process
-
- C—CHEMISTRY; METALLURGY
- C23—COATING 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
- C23C—COATING 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
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/04—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
- C23C4/06—Metallic material
- C23C4/073—Metallic material containing MCrAl or MCrAlY alloys, where M is nickel, cobalt or iron, with or without non-metal elements
Definitions
- the present invention relates to metallic coatings based on wear-resistant and corrosion-resistant amorphous alloys, the processes for obtaining these coatings and their applications to the production of anti-wear coatings, in particular for hydraulic equipment.
- One of the solutions for obtaining materials having a satisfactory compromise between these contradictory properties consists in using metal alloys of amorphous structure obtained by rapid cooling.
- the amorphous alloys used to date are essentially in the form of small ribbons obtained by a casting method or in the form of very thin deposits obtained by electrochemical methods.
- the thermal projection methods and for example that of the blown arc plasma have not so far made it possible to obtain completely amorphous alloys at the level of X-ray diffraction in the form of very thick powder deposits (> 0.5 mm) on surfaces up to several square meters.
- the object of the present invention is to provide amorphous metallic coatings combining with high mechanical characteristics a certain ductility, a high crystallization temperature, a good ability to be released from the residual manufacturing constraints by means of a heat treatment of stress relaxation without causing a significant change in structure and brittleness, good corrosion resistance, including in the presence of halogens, made from alloys capable of being amorphizable for cooling rates of the around 105K / sec., these coatings can be obtained in thicknesses from 0.03 to 1.5 mm on large surfaces.
- the inventors have discovered that the ease of amorphization can be obtained by combining the action of the different states of positive or negative size of certain constituent elements with respect to the basic constituent elements, and in particular by playing on the combined action of B and Zr on a matrix of Fe - Ni and and / or Co.
- the powders of these alloys are obtained by atomization and, for grain sizes ⁇ 100 ⁇ m, the grains have a completely amorphous structure by X-ray diffraction.
- the thermal spray deposition method allows reproducibility of deposition and structural conditions.
- the alloys used for the amorphous metallic coatings resistant to wear and erosion according to the invention have many advantages compared to the alloys of the prior art. First of all, these are easily amorphizable alloys due to the simultaneous presence of boron, an element whose atomic dimension is smaller than that of T atoms, and of Zr, larger than T atoms.
- the crystallization temperature of these alloys is remarkably high, when compared to that of alloys of the prior art, such as Fe-B alloys and derived alloys (such as Fe - B - C, Fe - B - Si ).
- This effect which can be attributed to the presence of zirconium, can be further increased by the addition of refractory elements (such as Mo, Ti, V, Nb, Rh ...) or metalloids.
- refractory elements such as Mo, Ti, V, Nb, Rh .
- chromium and zirconium make it possible to obtain excellent resistance to corrosion, an effect which can be further reinforced by the addition of various elements, in particular Rh, Nb, Ti, rare earths and phosphorus.
- these are essentially ductile metallic glasses in a sufficiently low metalloid concentration range, namely: b + g ⁇ 24 at%.
- the alloys obtained then resist satisfactorily the embrittlement which usually follows in other alloys the heat treatments at the crystallization temperature.
- Example 1 Elaboration of alloys corresponding to the general formulation of family (II)
- Alloys corresponding to the formulation of family (II) have been prepared in the liquid state from the constituents, taken separately. For this, fragments of the elements, of commercial purity, were alloyed in the liquid state in a cold hearth furnace placed under helium. The components were heated by high frequency currents. After melting, these alloys are introduced into the inductor of a tape casting machine consisting of a copper wheel 250 mm in diameter having a tangential speed of 35 m / sec. The enclosure containing the wheel is in a helium atmosphere. The crucible is made of quartz with an orifice 0.8 mm in diameter. The injection pressure of the liquid metal is 0.5 bar. The temperature of the liquid metal is measured by optical pyrometry on the upper face of the liquid.
- the concentration, in atom%, of the chemical elements is as follows: 50 ⁇ Ni ⁇ 75 0 ⁇ Mo ⁇ 5 5 ⁇ Cr ⁇ 25 0 ⁇ Hf ⁇ 5 5 ⁇ Zr ⁇ 15 0 ⁇ If ⁇ 5 5 ⁇ B ⁇ 15 0 ⁇ La ⁇ 4
- the concentration, in atom%, of the chemical elements is as follows: 10 ⁇ Fe ⁇ 75 5 ⁇ Zr ⁇ 15 0 ⁇ Hf ⁇ 4 10 ⁇ Ni ⁇ 60 5 ⁇ B ⁇ 15 0 ⁇ Nb ⁇ 4 5 ⁇ Cr ⁇ 15 0 ⁇ Mo ⁇ 12 0 ⁇ La ⁇ 4 O ⁇ Ti ⁇ 10
- Alloys corresponding to the formulation of family (IV) were developed and obtained in the form of ribbons in an identical manner to that which was done for obtaining the alloys of the preceding examples.
- the concentration, in atom%, of the chemical elements is as follows: 50 ⁇ Co ⁇ 82 5 ⁇ B ⁇ 15 3 ⁇ Ni ⁇ 35 0 ⁇ Mo ⁇ 12 5 ⁇ Zr ⁇ 15 5 ⁇ Cr ⁇ 15 0 ⁇ La ⁇ 4
- Alloys corresponding to the formulation of family (V) were developed and obtained in the form of ribbons in an identical manner to that which was done for obtaining the alloys of the preceding examples.
- the concentration, in atom%, of the chemical elements is as follows: 10 ⁇ Fe ⁇ 65 5 ⁇ Cr ⁇ 15 10 ⁇ Co ⁇ 65 5 ⁇ B ⁇ 15 5 ⁇ Zr ⁇ 15 10 ⁇ Ni ⁇ 65 1 ⁇ C ⁇ 5 O ⁇ If ⁇ 5 1 ⁇ P ⁇ 9
- Example 5 Elaboration of alloys corresponding to the general formulation of the family (V)
- Alloys corresponding to the formulation of family (V) were developed and obtained in the form of ribbons in an identical manner to that which was done for obtaining the alloys of the preceding examples.
- the concentration, in atom%, of the chemical elements is as follows: 10 ⁇ Fe ⁇ 50 5 ⁇ Cr ⁇ 15 10 ⁇ Co ⁇ 50 5 ⁇ B ⁇ 15 5 ⁇ Zr ⁇ 15 10 ⁇ Ni ⁇ 50 0 ⁇ C ⁇ 5 O ⁇ If ⁇ 17 0 ⁇ P ⁇ 9
- the alloys powders of families (II) to (V) were deposited on various metallic substrates such as structural steel, stainless steels, copper-based alloys, by a thermal spraying method, and for example by the method of arc plasma blown under controlled atmosphere and temperature.
- These projected powders have a particle size between 30 and 100 ⁇ m.
- the thicknesses, deposited on a sanded substrate, are between 0.03 and 1.5 mm.
- the coated surfaces are covered over several square meters.
- the deposits are made under the conditions described in Example 9. However, according to one embodiment of the method according to the invention, instead of working in a controlled atmosphere, in order to prevent any oxidation during the spraying of the molten powders, the only path of the molten particles is protected by an annular jet of nitrogen, concentric with the jet of plasma carrying the particles, and of dimensions slightly greater than this. The deposits can then be carried out in the open air, under partial nitrogen protection.
- the thermal mass of the part may be sufficient to provide cooling allowing the deposit to have an amorphous structure. This avoids the cryogenic cooling step.
- the curves represented in FIG. 8 correspond to a composition in at%: Fe20; Ni28; Co20; Cr12; Zr10; B10.
- Isothermal anneals define the stability domains of amorphous (A) and crystallized (C) structures for a given time and temperature.
- the curve represented in FIG. 9 illustrates the results for the anisothermal anneals which define the start of the crystallization temperature as a function of the heating rate.
- the deposits of thickness of the order of 0.5 mm obtained by the thermal spraying method according to the invention have, in the raw state of deposition, a percentage of porosity of the order of 8% measured by treatment d 'picture.
- This porosity rate can be reduced to close to 0 by a shot peening of the deposit from carbon steel or stainless steel balls with a diameter between 1 and 1.6 mm for a defined peening intensity (Halmen de la Sté Metal Improvment) from 16 to 18 and a recovery rate (Metal Improvment method) of 600%.
- the deposits were tested under conditions of wear by abrasive erosion identical to that occurring on the materials of hydraulic machines operating in an aqueous medium loaded with fine particles of solid material such as quartz.
- the wear measured at room temperature for deposition is equivalent to ceramic wear such as, for example, Cr2O3 and is significantly lower than metal alloys such as stellite, stainless steels such as dupleix or martensito-ferritic, as well as commercial steels known as resistant to abrasion.
- Dry abrasive erosion tests at angles of incidence ranging from 0 to 90 ° give better behavior of the amorphous alloys according to the invention compared to ceramics and other metal alloys.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- Plasma & Fusion (AREA)
- Powder Metallurgy (AREA)
- Coating By Spraying Or Casting (AREA)
- Soft Magnetic Materials (AREA)
- Physical Vapour Deposition (AREA)
- Manufacture Of Metal Powder And Suspensions Thereof (AREA)
- Chemically Coating (AREA)
- Electroplating Methods And Accessories (AREA)
- Magnetic Heads (AREA)
- Supporting Of Heads In Record-Carrier Devices (AREA)
- Analysing Materials By The Use Of Radiation (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
- Glass Compositions (AREA)
- Laminated Bodies (AREA)
- Sampling And Sample Adjustment (AREA)
- Chemical Vapour Deposition (AREA)
- Battery Electrode And Active Subsutance (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Mechanical Operated Clutches (AREA)
- Contacts (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9206535 | 1992-05-22 | ||
FR9206535A FR2691478B1 (fr) | 1992-05-22 | 1992-05-22 | Revêtements métalliques à base d'alliages amorphes résistant à l'usure et à la corrosion, rubans obtenus à partir de ces alliages, procédé d'obtention et applications aux revêtements antiusure pour matériel hydraulique. |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0576366A1 EP0576366A1 (fr) | 1993-12-29 |
EP0576366B1 true EP0576366B1 (fr) | 1996-03-27 |
Family
ID=9430266
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP93420202A Expired - Lifetime EP0576366B1 (fr) | 1992-05-22 | 1993-05-18 | Revêtements métalliques à base d'alliages amorphes résistant à l'usure et à la corrosion, procédé d'obtention et applications aux revêtements anti-usure pour matériel hydraulique |
Country Status (18)
Country | Link |
---|---|
US (2) | US5376191A (no) |
EP (1) | EP0576366B1 (no) |
JP (1) | JPH0688175A (no) |
KR (1) | KR100271996B1 (no) |
CN (1) | CN1049457C (no) |
AT (1) | ATE136062T1 (no) |
AU (1) | AU664265B2 (no) |
BR (1) | BR9301937A (no) |
CA (1) | CA2096682A1 (no) |
DE (1) | DE69301965T2 (no) |
DK (1) | DK0576366T3 (no) |
ES (1) | ES2085132T3 (no) |
FI (1) | FI100891B (no) |
FR (2) | FR2691478B1 (no) |
GR (1) | GR3019445T3 (no) |
MX (1) | MX9302977A (no) |
NO (1) | NO300553B1 (no) |
ZA (1) | ZA933517B (no) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8075712B2 (en) | 2005-11-14 | 2011-12-13 | Lawrence Livermore National Security, Llc | Amorphous metal formulations and structured coatings for corrosion and wear resistance |
Families Citing this family (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3547098B2 (ja) * | 1994-06-06 | 2004-07-28 | トヨタ自動車株式会社 | 溶射方法、溶射層を摺動面とする摺動部材の製造方法、ピストンおよびピストンの製造方法 |
US5531176A (en) * | 1994-06-16 | 1996-07-02 | Johnson; Adrienne M. | Method of making an applique |
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- 1993-05-14 US US08/060,985 patent/US5376191A/en not_active Expired - Fee Related
- 1993-05-18 EP EP93420202A patent/EP0576366B1/fr not_active Expired - Lifetime
- 1993-05-18 ES ES93420202T patent/ES2085132T3/es not_active Expired - Lifetime
- 1993-05-18 DE DE69301965T patent/DE69301965T2/de not_active Expired - Fee Related
- 1993-05-18 DK DK93420202.9T patent/DK0576366T3/da active
- 1993-05-18 AU AU38672/93A patent/AU664265B2/en not_active Ceased
- 1993-05-18 AT AT93420202T patent/ATE136062T1/de not_active IP Right Cessation
- 1993-05-18 NO NO931800A patent/NO300553B1/no not_active IP Right Cessation
- 1993-05-19 ZA ZA933517A patent/ZA933517B/xx unknown
- 1993-05-19 FI FI932289A patent/FI100891B/fi not_active IP Right Cessation
- 1993-05-19 BR BR9301937A patent/BR9301937A/pt not_active IP Right Cessation
- 1993-05-20 CA CA002096682A patent/CA2096682A1/en not_active Abandoned
- 1993-05-21 JP JP5120170A patent/JPH0688175A/ja active Pending
- 1993-05-21 MX MX9302977A patent/MX9302977A/es not_active IP Right Cessation
- 1993-05-22 KR KR1019930008925A patent/KR100271996B1/ko not_active IP Right Cessation
- 1993-05-22 CN CN93106300A patent/CN1049457C/zh not_active Expired - Fee Related
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1994
- 1994-06-01 US US08/251,947 patent/US5421919A/en not_active Expired - Fee Related
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US8075712B2 (en) | 2005-11-14 | 2011-12-13 | Lawrence Livermore National Security, Llc | Amorphous metal formulations and structured coatings for corrosion and wear resistance |
US8778460B2 (en) | 2005-11-14 | 2014-07-15 | Lawrence Livermore National Security, Llc. | Amorphous metal formulations and structured coatings for corrosion and wear resistance |
Also Published As
Publication number | Publication date |
---|---|
EP0576366A1 (fr) | 1993-12-29 |
ES2085132T3 (es) | 1996-05-16 |
AU664265B2 (en) | 1995-11-09 |
FI932289A (fi) | 1993-11-23 |
AU3867293A (en) | 1993-11-25 |
FR2691478A1 (fr) | 1993-11-26 |
ZA933517B (en) | 1993-12-10 |
ATE136062T1 (de) | 1996-04-15 |
DE69301965T2 (de) | 1996-09-12 |
CN1049457C (zh) | 2000-02-16 |
JPH0688175A (ja) | 1994-03-29 |
CN1088630A (zh) | 1994-06-29 |
MX9302977A (es) | 1994-02-28 |
KR100271996B1 (ko) | 2000-12-01 |
CA2096682A1 (en) | 1993-11-23 |
FI100891B (fi) | 1998-03-13 |
DE69301965D1 (de) | 1996-05-02 |
US5421919A (en) | 1995-06-06 |
NO931800D0 (no) | 1993-05-18 |
DK0576366T3 (da) | 1996-07-29 |
BR9301937A (pt) | 1993-11-30 |
KR930023483A (ko) | 1993-12-18 |
FR2691478B1 (fr) | 1995-02-17 |
GR3019445T3 (en) | 1996-06-30 |
FI932289A0 (fi) | 1993-05-19 |
NO931800L (no) | 1993-11-23 |
FR2691477B1 (fr) | 1994-08-26 |
NO300553B1 (no) | 1997-06-16 |
US5376191A (en) | 1994-12-27 |
FR2691477A1 (fr) | 1993-11-26 |
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