EP0229478A2 - Alliages microcristallins préparés à partir de poudres d'alliages métalliques amorphes ou désordonnés obtenus par réaction en phase solide - Google Patents
Alliages microcristallins préparés à partir de poudres d'alliages métalliques amorphes ou désordonnés obtenus par réaction en phase solide Download PDFInfo
- Publication number
- EP0229478A2 EP0229478A2 EP86309337A EP86309337A EP0229478A2 EP 0229478 A2 EP0229478 A2 EP 0229478A2 EP 86309337 A EP86309337 A EP 86309337A EP 86309337 A EP86309337 A EP 86309337A EP 0229478 A2 EP0229478 A2 EP 0229478A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- microcrystalline
- alloy
- amorphous
- metal alloy
- solid state
- 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.)
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Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F9/00—Making metallic powder or suspensions thereof
- B22F9/002—Making metallic powder or suspensions thereof amorphous or microcrystalline
- B22F9/007—Transformation of amorphous into microcrystalline state
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F1/00—Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
- B22F1/14—Treatment of metallic powder
- B22F1/142—Thermal or thermo-mechanical treatment
Definitions
- This invention relates to the preparation of microcrystalline alloys from amorphous or disordered metal alloy powder precursors. More specifically, this invention relates to the synthesis of microcrystalline alloys from amorphous or disordered metal alloy powders prepared by the interdiffusion of intimately mixed precursor materials during solid state reaction processes and novel microcrystalline compositions obtained therefrom.
- Microcrystalline alloys have become of interest in the area of structural and engineered materials due to their mechanical, physical, wear and corrosion resistant properties. These alloys are chracterized by many random nucleation sites, each having separate crystallinity, but whose growth has been inhibited, due to the growth of adjacent nucleation sites. This is different from true crystalline materials, which result from the continued growth of one nucleation site, forming a longer range, continuous ordered structure. The fine grained structure resulting from the numerous small nucleation sites is responsible for the improved mechanical and wear resistant properties of microcrystalline alloys, compared to polycrystalline materials. Microcrystalline alloys may possess high tensile strength, high thermal stability, and high ductility depending on the prevalent chracteristics of the elemental components of the individual microcrystalline alloy. These materials are of special interest for use as tool steel alloys, such as cutting tools, dies, and other similar metal products, which require high strength properties, as well as high temperature performance and oxidation resistance.
- Microcrystalline alloys can be formed by heat-treating amorphous metal alloy powders at a temperature above the crystallization temperature of the powder. This is done for a period of time sufficient to produce the microcrystalline material, but not so long as to form a substantially crystalline material.
- the compositional range of the amorphous alloy material is retained during the microcrystallization heat-treatment, and present in the microcrystalline material formed.
- the composition and homogeneity of the amorphous or disordered metal alloy powder precursor therefore, determine the degree to which various desired microcrystalline alloy characteristics, such as hardness, ductility and heat performance will exist in the resultant microcrystalline alloy.
- amorphous metal alloy materials are prepared by rapid solidification processing (RSP) from a molten precursor phase.
- RSP rapid solidification processing
- the amorphous metal alloy material is then heat-treated at a temperature above the crystallization temperature of the material for a time necessary to form its microcrystalline counterpart.
- the RSP technique to form amorphous metal alloys has found great commercial success, as a variety of known alloys can be manufactured by this technique in various forms such as thin films, ribbons and wires.
- the technique involves subjecting a melt of the amorphous metal alloy composition to be made to rapid cooling rates on the order of 10-10 °C/sec.
- This method is taught by United States Patent No. 3,856,513 to Chen et al., which discloses directing a stream of the molten metal into the nip of rotating double rolls maintained at room temperature, which quenchs the metal in. the form of an amorphous ribbon, thin film, wire, or platelet.
- an amorphous or disordered metal alloy powder from an RSP-prepared material requires mechanically reducing the amorphous metal alloy material as by chipping, crushing, grinding or ball milling.
- the resultant powder is then heat-treated at a temperature above the crystallization temperature of the amorphous metal alloy for a period of time necessary to cause microcrystallization to occur.
- United States Patents Nos. 4,400,212 and 4,410,490 to Ray disclose the production of cobalt-chromium-carbon and cobalt-nickel-tungsten-carbon microcrystalline alloys, respectively, by the RSP method described above.
- United States Patent No. 4,473,402 also to Ray, discloses the consolidation, as by hot extrusion or cold pressing and sintering, of amorphous powder cobalt-chromium-carbide compositions prepared by the RSP technique to produce microcrystalline alloys. Ray reports a range of microcrystalline alloy material compositions which is wider than previously achieved composition ranges.
- the RSP process for making amorphous metal alloys suffers from the disadvantage that the so-formed amorphous alloy is produced in a limited shape, that is as a thin-film such as a ribbon, wire or platelet. While there are a few direct uses for amorphous metal ribbons, most often a comminution step is required to obtain a more readily usable amorphous alloy powder, as is required to prepare microcrystalline alloys. The comminution step often results, to some extent, in a loss of homogeneity between the ribbon and powder stages. Further, comminution of the amorphous alloy, and subsequent recombination in a desired bulk shape, is a difficult process when it is realized that most amorphous metal alloys have high mechanical strengths and also possess high hardnesses.
- An alternative method to RSP techniques is the use of solid state reaction processes to produce amorphous or disordered metal alloy powders.
- Such a process is disclosed in International Application Number PCT/US84/00035, published under the Patent Cooperation Treaty, to Johnson et al.
- the process disclosed therein relates to the production of amorphous or fine crystalline materials by solid state reactions. This process comprises contacting two or more materials such that they undergo chemical reaction resulting in the diffusion of the materials into one another, and heating the materials at a temperature which permits the chemical reaction to occur, thus forming a metastable solid. Reacting at a temperature near the crystallization temperature may form a fine crystalline alloy. This process further requires that the phase formed have a lower free energy than the sum of the free energies of the starting components.
- microcrystalline alloy preparation from powders is a simple process for the direct formation of a large variety of microcrystalline alloy compositions from amorphous or disordered metal alloy powders. Especially lacking is a simple process that would synthesize amorphous metal alloy materials directly as powders which may undergo immediate heat treatment to produce microcrystalline alloys without loss of homogeneity.
- the present invention relates to a process for the synthesis of a microcrystalline alloy, comprising heat treating a substantially amorphous or disordered metal alloy powder, prepared by the interdiffusion of intimately mixed precursor materials during a solid state reaction process, at a temperature sufficiently above the crystallization temperature to form the microcrystalline alloy.
- the invention further relates to a microcrystalline alloy prepared by heat-treating a substantially amorphous or disordered metal alloy powder, prepared by the interdiffusion of intimately mixed precursor materials during a solid state reaction process, at a temperature sufficiently above the crystallization temperature to form the microcrystalline alloy.
- the invention relates to a microcrystalline alloy characterized in that the free energy of the alloy is greater than that of a rapidly solidified material of about the same composition, and a process for producing the same.
- microcrystalline alloy as used herein refers to an alloy material characterized by a crystalline grain size of about 0.01 microns to about 1.0 microns.
- amorphous metal alloy connotes amorphous metal-containing alloys that may also comprise nonmetallic elements.
- substantially with respect to the amorphous metal alloy powder means that the powders used to prepare the microcrystalline alloys are at least 50 percent amorphous, preferably at least 80 percent amorphous, and most preferably about 100 percent amorphous.
- the processes disclosed herein provide for the formation of microcrystalline alloys from amorphous or disordered metal alloy powder precursors prepared by solid state reaction methods.
- Solid state reaction preparation of the amorphous alloy produces the alloy in powder form, thus avoiding the need for comminution and increasing retention of the chemical homogeneity of the amorphous material in the subsequently produced microcrystalline alloy.
- These solid state reaction methods yield direct synthesis of amorphous or disordered metal alloy compositions in powder form far from the equilibrium composition. This highly non-equilibrium state influences the transformation from amorphous metal alloy powder to microcrystalline alloy in such a manner that these processes yield a microcrystalline alloy with increased compositional diversity and commensurate diversity with respect to physical properties.
- the solid state reaction employed can vary depending on the desired alloy composition and properties. Some adaptable solid state reaction methods include chemical reduction reactions and thermal decomposition reactions. Each reaction method yields a powder alloy composition which is formed by the interdiffusion of the initial components absent the necessity of chemically reacting those initial components. This composition may be amorphous or be made amorphous by heat-treating at a temperature and pressure below that necessary for crystallization. The resultant amorphous or disordered powder, as taught herein, is suitable to undergo heat-treatment to the microcrystalline phase.
- Solid state chemical reduction for the synthesis of amorphous or disordered metal alloy powder precursors is disclosed in United States Patent No. 4,537,625, entitled “Amorphous Metal Alloy Powders and Synthesis of Same by Solid State Chemical Reduction Reactions.”
- This process comprises disposing a precursor compound in a liquid medium and reducing this compound to obtain a substantially amorphous metal alloy. More specifically, the process, as disclosed, involves dissolving the precursor compound in a solvent to form a solution and reducing the compound, which causes formation of a precipitate. This precipitate is an intimate mixture of the components of the amorphous metal alloy to be synthesized.
- the reduction which preferably occurs in the absence of oxygen and at a temperature below crystallization temperature, can be accomplished by addition of a reducing agent to the solution, or by other reducing methods, such as electrochemical reduction or photocatalytic reduction. Subsequent heat-treatment at a temperature below the crystallization temperature of the amorphous metal alloy to be formed causes transition to the amorphous phase.
- Solid state thermal decomposition is another method by which amorphous metal alloys may be formed.
- United States Patent No. 4,537,624, entitled “Amorphous Metal Alloy Powders and Synthesis of Same by Solid State Decomposition Reactions,” teaches such a process.
- This process includes the step of thermally decomposing a precursor compound at a temperature below the crystallization temperature of the amorphous metal alloy to be formed.
- the decomposition of the precursor material may occur in a partial or full vacuum, or under an inert, reducing, or reactive atmosphere.
- the precursor components may alloy during the decomposition step if the temperature and timing are conducive to alloying of the given components.
- solid state reaction methods recited above yield amorphous or disordered metal alloy powders in a high non-equilibrium state.
- This high free energy state is characterized by higher molecular disorder than the melt phase employed with RSP for compounds having similar compositions.
- Solid state reactions produce stable amorphous or disordered alloy materials having much greater compositional diversity than can be obtained using RSP techniques which produce materials that generally consist of equilibrium phase compounds.
- the resultant amorphous or disordered alloy powder embodying variations in composition due to the high free energy of this material, is then heat-treated, in accordance with this disclosure, to form the microcrystalline alloy.
- Solid state reaction processes such as those discussed above, increase the range of compositions that will exist in any given microcrystalline alloy. By increasing the range of compositions, a commensurate increase in the range of properties, characteristic to different compositions, is achieved, thus making solid state reactions desirable for microcrystalline alloy production.
- the amorphous metal alloy powders produced by the solid state reactions discussed above, or any other solid state reaction methods, can be compacted to a desired shape, or left in the powder form, and heat-treated to a temperature between about 0.6 and 0.95 of the solidus temperature of the amorphous or disordered metal alloy powder to produce the microcrystalline alloy.
- the heat-treatment process to the microcrystalline phase occurs over a period of from about 1 hour to about 1,000 hours, depending on the amorphous or disordered metal alloy composition used and the treatment temperature.
- This example illustrates the formation of a microcrystalline alloy composition of iron-nickel-boron from an amorphous or disordered metal alloy powder prepared under solid state reduction conditions.
- the solution was cannulated away from the precipitate and the precipitate was then washed with two 50 ml portions of distilled water.
- the precipitate was then dried under a vacuum at about 60°C for about four hours. In this condition, the black precipitate powder reacts vigorously upon exposure to oxygen, and so should be maintained in the absence of oxygen.
- the powder was then transferred under inert conditions to a quartz tube, which was sealed under vacuum, and was heat-treated at about 290°C for 264 hours. This produced a powder consisting substantially of amorphous material.
- a portion of the powder was further heat-treated at about 900°C for one hour to produce a silver, cohesive agglomeration which reacted slightly upon exposure to oxygen.
- X-ray diffraction data of the material indicated a microcrystalline alloy of the approximate composition Fe 8 Ni 2 B consisting of multiple phases.
- Example 1 The procedure described in Example 1 was repeated with the exception that the heat-treatment of the amorphous or disordered metal alloy powder to form the microcrystalline alloy was carried out at about 600°C for about one hour.
- the resultant alloy was determined to be microcrystalline and to have about the same composition, Fe 8 Ni 2 B, as in Example 1. This illustrates that the temperature of this heat-treatment need only be sufficiently above the crystallization temperature, and that a broad range of temperatures beyond the crystallization temperature may be employed. This temperature range will vary, of course, depending on the elemental components of a given amorphous metal alloy powder precursor.
- This mixture was then washed with two 100 ml portions of distilled water and dried under vacuum at 60°C for 4 hours. Under vacuum, this material was heated to 200°C for 20.5 hours to remove any H 2 from the powder. The material was then sealed in a quartz tube and heat-treated at 840°C to produce a microcrystalline material of the composition Nd 15 Fe 61 Co 16 B 8 .
- microcrystalline alloy compositions from amorphous or disordered metal alloy powder precursors prepared by solid state reaction methods.
- This novel application of solid state reaction methods to form particulate precursor compounds as amorphous or disordered metal alloy powders, existing in a high free energy state, followed by microcrystallization heat-treatment processing, may facilitate retention of some of the highly disordered state of the system in the resultant microcrystalline alloy material.
- these materials and processing techniques may also make resultant materials useful as strengthening aids.
- Materials which could be altered to produce novel composites may include crystalline metal powders, ceramics and plastics.
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- Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Powder Metallurgy (AREA)
- Manufacture Of Metal Powder And Suspensions Thereof (AREA)
- Soft Magnetic Materials (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US81542985A | 1985-12-31 | 1985-12-31 | |
| US815429 | 1985-12-31 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0229478A2 true EP0229478A2 (fr) | 1987-07-22 |
| EP0229478A3 EP0229478A3 (fr) | 1988-11-17 |
Family
ID=25217763
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP86309337A Withdrawn EP0229478A3 (fr) | 1985-12-31 | 1986-12-01 | Alliages microcristallins préparés à partir de poudres d'alliages métalliques amorphes ou désordonnés obtenus par réaction en phase solide |
Country Status (6)
| Country | Link |
|---|---|
| EP (1) | EP0229478A3 (fr) |
| JP (1) | JPS62170401A (fr) |
| AU (1) | AU6676986A (fr) |
| BR (1) | BR8606422A (fr) |
| CA (1) | CA1292630C (fr) |
| IN (1) | IN165517B (fr) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7048809B2 (en) * | 2003-01-21 | 2006-05-23 | Metglas, Inc. | Magnetic implement having a linear BH loop |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1217049A (fr) * | 1958-11-18 | 1960-04-29 | Commissariat Energie Atomique | Procédé d'élaboration de masses métalliques poreuses ou non par frittage non thermique |
| US4564396A (en) * | 1983-01-31 | 1986-01-14 | California Institute Of Technology | Formation of amorphous materials |
| AU571655B2 (en) * | 1984-03-05 | 1988-04-21 | Standard Oil Company, The | Amorphous metal alloy powders and articles derived therefrom |
| US4537625A (en) * | 1984-03-09 | 1985-08-27 | The Standard Oil Company (Ohio) | Amorphous metal alloy powders and synthesis of same by solid state chemical reduction reactions |
| DE3418209A1 (de) * | 1984-05-16 | 1985-11-21 | Siemens AG, 1000 Berlin und 8000 München | Verfahren zur herstellung eines metallischen koerpers unter verwendung einer amorphen legierung |
-
1986
- 1986-06-25 IN IN556/DEL/86A patent/IN165517B/en unknown
- 1986-11-20 CA CA000523435A patent/CA1292630C/fr not_active Expired - Fee Related
- 1986-12-01 EP EP86309337A patent/EP0229478A3/fr not_active Withdrawn
- 1986-12-19 AU AU66769/86A patent/AU6676986A/en not_active Abandoned
- 1986-12-23 BR BR8606422A patent/BR8606422A/pt unknown
- 1986-12-27 JP JP61315913A patent/JPS62170401A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| BR8606422A (pt) | 1987-10-20 |
| JPS62170401A (ja) | 1987-07-27 |
| IN165517B (fr) | 1989-11-04 |
| AU6676986A (en) | 1987-07-02 |
| EP0229478A3 (fr) | 1988-11-17 |
| CA1292630C (fr) | 1991-12-03 |
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| 18D | Application deemed to be withdrawn |
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| RIN1 | Information on inventor provided before grant (corrected) |
Inventor name: TENHOVER, MICHAEL ALAN Inventor name: HENDERSON, RICHARD SCOTT Inventor name: GRASSELLI, KARL ROBERT |