US2966731A - Aluminum base alloy powder product - Google Patents

Aluminum base alloy powder product Download PDF

Info

Publication number
US2966731A
US2966731A US724226A US72422658A US2966731A US 2966731 A US2966731 A US 2966731A US 724226 A US724226 A US 724226A US 72422658 A US72422658 A US 72422658A US 2966731 A US2966731 A US 2966731A
Authority
US
United States
Prior art keywords
aluminum
alloy
base alloy
aluminum base
manganese
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
Application number
US724226A
Inventor
Raymond J Towner
Jr John P Lyle
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.)
Howmet Aerospace Inc
Original Assignee
Aluminum Company of America
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 Aluminum Company of America filed Critical Aluminum Company of America
Priority to US724226A priority Critical patent/US2966731A/en
Application granted granted Critical
Publication of US2966731A publication Critical patent/US2966731A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C1/00Making non-ferrous alloys
    • C22C1/04Making non-ferrous alloys by powder metallurgy
    • C22C1/0408Light metal alloys
    • C22C1/0416Aluminium-based alloys
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S75/00Specialized metallurgical processes, compositions for use therein, consolidated metal powder compositions, and loose metal particulate mixtures
    • Y10S75/95Consolidated metal powder compositions of >95% theoretical density, e.g. wrought

Definitions

  • This invention relates to articles made from aluminum base alloy powders and it is more particularly concerned with those products resulting from heating and working a compacted mass of atomized particles of an aluminum manganese base alloy.
  • the aluminum-manganese powder products can be readily worked under the usual hot working conditions of temperature and pressure employed in fabricating conventional aluminum and aluminum base alloy articles. Furthermore, the hot-worked product can be cold worked to a limited extent, if desired.
  • the fabricated aluminum alloy products can be placed in service without any preliminary thermal treatment. The strength of the wrought powder products at elevated temperatures is not influenced to any significant extent by the oxide film which coats the atomized particles.
  • the atomized alloy particles are preferably prepared by melting the alloy of the desired composition and pro jecting it through a suitably designed nozzle with the which possess unique strength properties at elevated temperatures.
  • the particles of oxide distributed throughout the body appear to impart the unusual strength at elevated temperatures.
  • the production of the oxide coated flakes is time consuming and consequently expensive. It has now been found, contrary to previous belief, that useful articles can be made from certain types of atomized aluminum alloy powders.
  • the atomization process involves disintegrating a stream of molten metal with a jet of gas, such as compressed air or by mechanical means. Very finely divided particles can be produced by this process that will pass through a standard Tyler 100 mesh screen.
  • Another object is to provide such articles which do not require any preliminary thermal treatment to place them in condition for service at elevated temperatures.
  • Still another object is to provide an article made from atomized aluminum-manganese alloy powder that does not depend upon the presence of oxide particles to impart strength at elevated temperatures.
  • a wrought aluminum base alloy nominally composed of aluminum, 12.2% silicon, 1.1% magnesium, 0.9% nickel and 0.9% copper has in the solution heat treated and age hardened condition a tensile strength of only 5,000 p.s.i. and a yield strength of 3,000 p.s.i. after exposure at 600 F. for 100 hours.
  • a second well-known aluminum base alloy nominally consisting of aluminum, 4.5% copper, 1.5% m gnesium and 0.6% manganese, when worked, solution heat treated and age hardened, has a tensile strength of 10,000 p.s.i. and a yield strength of 7,500
  • the atomizing conditions should be'so adjusted that none or only a small proportion of the particles are larger than mesh 'imicrons opening) and that the majority of the particles will pass through a 200 mesh screen (74 microns open- 20 ing).
  • the particles produced in this manner generally have an irregular shape but for the most part are substantially equiaxed in dimensions and have as-cast structure.
  • the aluminum-manganese constituent in the alloy is very finely divided as a result of the drastic chill associated with the atomization process.
  • the surfaces of the particles are, of course, oxidized if the atomization has occurred in air or in some other oxidizing atmosphere, however, the oxide skin is very thin and the amount of oxide introduced into the final product is too small to affect the properties thereof to any significant extent.
  • the manganese content of the alloy should be between 1.5 and 15% by weight, as mentioned above, and preferably within the range of 5 to 10% to obtain the highest strength at elevated temperatures. If less than 1.5% is employed, the minimum strength is not achieved and if more than 15 is present, the worked article has insufiicient ductility and may fracture under ap lied stresses. Manganese is substantially insoluble in aluminum and whatever small proportion may be dissolved is too small to have any significant elfect upon the properties of the.
  • the matrix of the atomized particles consists of aluminum with a dispersion of finely divided aluminum-manganese constituent distributed throughout the particle.
  • the high strength at elevated temperatures appears to be controlled by the amount of the aluminum-manganese constituent and the fineness of the dispersion.
  • the alloy may contain the usual impurities associated With aluminum, for example, silicon and iron. Generally, the silicon impurity should not exceed 0.8% and the iron content should not be more than about 1%. Other impurities, such as copper, may also be present in amounts up to 0.5%. In view of the relatively small amount of iron impurity permitted in the alloy, the composition is referred to herein as being substantially ironfree.
  • the manganese content of the alloy should exceed the total amount of any added hardener elements.
  • the powder may be initially formed into a compact that is subsequently worked or it may be charged. directly to a-compression chamber, such as an extrusion press cylinder, and be extruded therefrom after initial consolidation of the mass.
  • the initial compact may be made by heatheated to 800 F. and extruded to diameter rod.
  • the Al-15.8% Mn alloy compact was heated to 1000 F. before being inserted in the extrusion press in order to improve the working quality of the compacts.
  • Tensile specimens were cut from the extruded rod and tested without any preliminary thermal treatment, some at room temperature and others at 600 F. after a 100-hour exposure at that temperature.
  • the composition of the alloys tested and the tensile properties at both room temejected, cooled, scalped, reheated to the hot working 10 perature and at 600 F. are given in Table 1 below.
  • the powder may be initially heated to a temperature between 700 and 900 F. and introduced to the chamber or it may be charged cold and heated within the chamber. Alternatively, it may be heated to an intermediate temperature, then charged to the chamber and brought to the desired temperature.
  • the powder When the powder is to be compacted and immediately extruded, it is generally convenient to compress the powdered mass against a blind die in a press cylinder and then substitute an extrusion die for it to produce the desired extruded shape.
  • an extrusion die for it to produce the desired extruded shape.
  • the hot working is preferably performed within the temperature range of 700 to 900 F.
  • Our invention is illustrated by the following examples wherein aluminum-manganese atomized powders were consolidated and the product hot worked.
  • the powders were of a fineness such that approximately 75% passed through a 200 mesh screen and substantially all of the remainder passed through a 100 mesh screen.
  • Each alloy powder was chargedto an extrusion press cylinder preheated to 800 F. and compressed against a blind die under a pressure of 100,000 p.s.i. for a period of approximately one minute. In the course of charging and compressing the powder the temperature of the compact reached 700-800 F.
  • the compact was either ejected from the cylinder, and subsequently hot worked or it was retained in the cylinder, an extrusion die having a diameter opening therein substituted for the blind die, and the compacted mass extruded to forma rod in diameter. Only the compact. of the Al1.6% Mn alloy was extruded directly after formation; the compacts of the other alloys were ejected from the cylinder, cooled, scalped and reheated for hot working.
  • a hot worked aluminum base alloy powder article free from aluminum oxide except as an incidental im purity and having a maximum iron content of 1% said hot worked alloy powder article being formed from atomized powder of an aluminum base alloy containing at least 70% by weight of aluminum and from 1.5 to 15% by weight of manganese as the essential component, the amount of said component exceeding the total quantity of any hardening elements present in the alloy, said alloy being substantially free from elements which form a solid solution with aluminum, except as they occur as impurities, said hot worked article being characterized in the as-worked condition by a tensile strength at 600 F. after a hour exposure of not less than 12,000 p.s.i. and a yield strength of not less than 10,000 p.s.i.
  • the alloy also contains at least one hardening element selected from the group consisting of nickel, cobalt, chromium, titanium, vanadium, molybdenum, Zirconium and tungsten in amounts of 0.1 to 10% each by weight, the total not exceeding 10% by Weight, the manganese content of said alloy exceeding the total amount of hardening elements added thereto.

Description

ALUM BASE ALLOY POWDER PRODUCT Raymond J. Towner and John P. Lyle, J12, New Kensington, Pa., assignors to Aluminum Company of America, Pittsburgh, Pa., a corporation of Pennsylvania No Drawing. Filed Mar. 27, 1958, Ser. No. 724,226
3 Claims. (Cl. 29-182) This invention relates to articles made from aluminum base alloy powders and it is more particularly concerned with those products resulting from heating and working a compacted mass of atomized particles of an aluminum manganese base alloy.
Heretofore, compressed and sintered bodies of oxidecoated aluminum flake powders have been produced p.s.i.
2,966,731 Patented Jan. 3, 1961 The aluminum-manganese powder products can be readily worked under the usual hot working conditions of temperature and pressure employed in fabricating conventional aluminum and aluminum base alloy articles. Furthermore, the hot-worked product can be cold worked to a limited extent, if desired. The fabricated aluminum alloy products can be placed in service without any preliminary thermal treatment. The strength of the wrought powder products at elevated temperatures is not influenced to any significant extent by the oxide film which coats the atomized particles.
The atomized alloy particles are preferably prepared by melting the alloy of the desired composition and pro jecting it through a suitably designed nozzle with the which possess unique strength properties at elevated temperatures. The particles of oxide distributed throughout the body appear to impart the unusual strength at elevated temperatures. The production of the oxide coated flakes is time consuming and consequently expensive. It has now been found, contrary to previous belief, that useful articles can be made from certain types of atomized aluminum alloy powders. As is Well known, the atomization process involves disintegrating a stream of molten metal with a jet of gas, such as compressed air or by mechanical means. Very finely divided particles can be produced by this process that will pass through a standard Tyler 100 mesh screen.
It is an object of this invention to provide articles having a high strength at elevated temperatures which are made from atomized particles of an aluminum base alloy containing manganese as the principal added alloy component.
Another object is to provide such articles which do not require any preliminary thermal treatment to place them in condition for service at elevated temperatures.
Still another object is to provide an article made from atomized aluminum-manganese alloy powder that does not depend upon the presence of oxide particles to impart strength at elevated temperatures.
These and other objects are achieved by atomizing a substantially iron-free aluminum base alloy containing not less than 70% by weight of aluminum and from 1.5 to 15% by weight of manganese as the principal added alloy component, and subsequently consolidating and working a mass of such atomized particles under the influence of heat and pressure. The resultant articles have a density closely approximating that of the alloy if.
cast; and in the hot worked condition, they have a tensile strength of not less than 12,000 p.s.i. and a minimum yield strength of 10,000 p.s.i. at 600 F. after a 100-hour exposure. These tensile and yield strength values ,are to be compared with those of some conventional wrought heat treated aluminum base alloys that have been recommended for service at elevated temperatures. For example, a wrought aluminum base alloy nominally composed of aluminum, 12.2% silicon, 1.1% magnesium, 0.9% nickel and 0.9% copper has in the solution heat treated and age hardened condition a tensile strength of only 5,000 p.s.i. and a yield strength of 3,000 p.s.i. after exposure at 600 F. for 100 hours. Under the same exposure conditions a second well-known aluminum base alloy nominally consisting of aluminum, 4.5% copper, 1.5% m gnesium and 0.6% manganese, when worked, solution heat treated and age hardened, has a tensile strength of 10,000 p.s.i. and a yield strength of 7,500
aid of a compressed gas. The atomizing conditions should be'so adjusted that none or only a small proportion of the particles are larger than mesh 'imicrons opening) and that the majority of the particles will pass through a 200 mesh screen (74 microns open- 20 ing). The particles produced in this manner generally have an irregular shape but for the most part are substantially equiaxed in dimensions and have as-cast structure. The aluminum-manganese constituent in the alloy is very finely divided as a result of the drastic chill associated with the atomization process. The surfaces of the particles are, of course, oxidized if the atomization has occurred in air or in some other oxidizing atmosphere, however, the oxide skin is very thin and the amount of oxide introduced into the final product is too small to affect the properties thereof to any significant extent.
The manganese content of the alloy should be between 1.5 and 15% by weight, as mentioned above, and preferably within the range of 5 to 10% to obtain the highest strength at elevated temperatures. If less than 1.5% is employed, the minimum strength is not achieved and if more than 15 is present, the worked article has insufiicient ductility and may fracture under ap lied stresses. Manganese is substantially insoluble in aluminum and whatever small proportion may be dissolved is too small to have any significant elfect upon the properties of the.
atomized particles. It will therefore be appreciated that the matrix of the atomized particles consists of aluminum with a dispersion of finely divided aluminum-manganese constituent distributed throughout the particle. The high strength at elevated temperatures appears to be controlled by the amount of the aluminum-manganese constituent and the fineness of the dispersion.
The alloy may contain the usual impurities associated With aluminum, for example, silicon and iron. Generally, the silicon impurity should not exceed 0.8% and the iron content should not be more than about 1%. Other impurities, such as copper, may also be present in amounts up to 0.5%. In view of the relatively small amount of iron impurity permitted in the alloy, the composition is referred to herein as being substantially ironfree.
For some purposes, it may be desirable to add one or more elements selected from the group composed of nickel. cobalt, chromium, titanium, vanadium, zirconium, molybdenum, and tungsten in amounts of 0.1 to 10% each, the total not exceeding 10%. These elements act as hardeners and, like manganese, are substantially insoluble in the aluminum matrix. To attain the properties attributable to the aluminum-manganese constituent, the manganese content of the alloy should exceed the total amount of any added hardener elements.
To make the Wrought article from the atomized powder, the powder may be initially formed into a compact that is subsequently worked or it may be charged. directly to a-compression chamber, such as an extrusion press cylinder, and be extruded therefrom after initial consolidation of the mass. The initial compact may be made by heatheated to 800 F. and extruded to diameter rod. The Al-15.8% Mn alloy compact was heated to 1000 F. before being inserted in the extrusion press in order to improve the working quality of the compacts. Tensile specimens were cut from the extruded rod and tested without any preliminary thermal treatment, some at room temperature and others at 600 F. after a 100-hour exposure at that temperature. The composition of the alloys tested and the tensile properties at both room temejected, cooled, scalped, reheated to the hot working 10 perature and at 600 F. are given in Table 1 below.
TABLE 1 Tensile properties of extruded AlMn powder products At Room Temperature At 600 F.
Alloy Percent Mn Tensile Yield Percent Tensile Yield Percent Strength, Strength, Elong. Strength, Strength, Elong.
p.s.i. p.s.i. p.s.i. p.s.i.
A 1.6 29. 900 22, 100 23 12, 400 10, 600 24 B 5.2 37. 900 25, 800 19. 8 15, 000 12, 800 25. 8 C 10.7 56.100 40. 600 5. 2 20, 400 14, 000 9. D 15.8""--- 63, 600 Broke 0 100 18, 100 1. 0 E 6.21 61, 100 42, 200 6. 20, 200 14, 400 19. 2 F tgMgi- 44, 400 35,600 1. 5 20, 400 16, 600 2. 2
.5 i. G 4.8 MEI-{ 44, 800 36,200 8. 2 13, 200 10,300 9. 8
temperature and hot worked. In some cases it may be It is apparent from the foregoing that the tensile and desirable to reheat the compact to temperatures as high yield strengths of the alloys increase with an increase as 1150 F. before hot working in order to obtain adequate workability. This should only be done if more than 3% manganese is present. Where the powder is charged to a compression chamber, it may be initially heated to a temperature between 700 and 900 F. and introduced to the chamber or it may be charged cold and heated within the chamber. Alternatively, it may be heated to an intermediate temperature, then charged to the chamber and brought to the desired temperature. When the powder is to be compacted and immediately extruded, it is generally convenient to compress the powdered mass against a blind die in a press cylinder and then substitute an extrusion die for it to produce the desired extruded shape. Although reference has been made to the extrusion of the powder mass, it is to be understood that it can be subjected to other types of hot working operations, such as rolling, forging or pressing, providing a suitable compact is initially produced. The hot working is preferably performed within the temperature range of 700 to 900 F.
Our invention is illustrated by the following examples wherein aluminum-manganese atomized powders were consolidated and the product hot worked. The powders were of a fineness such that approximately 75% passed through a 200 mesh screen and substantially all of the remainder passed through a 100 mesh screen. Each alloy powder was chargedto an extrusion press cylinder preheated to 800 F. and compressed against a blind die under a pressure of 100,000 p.s.i. for a period of approximately one minute. In the course of charging and compressing the powder the temperature of the compact reached 700-800 F. After the compact wasthus formed it was either ejected from the cylinder, and subsequently hot worked or it was retained in the cylinder, an extrusion die having a diameter opening therein substituted for the blind die, and the compacted mass extruded to forma rod in diameter. Only the compact. of the Al1.6% Mn alloy was extruded directly after formation; the compacts of the other alloys were ejected from the cylinder, cooled, scalped and reheated for hot working. The compacts of the Al5.2% Mn, Al 10.7% Mn, Al6.2% Mn4.9% Ni, Al4.9% Mn- 3.5% Ti, and Al-4.8% Mn4.7% Zr alloys were reheated to 850 F., inserted in an extrusion press cylinder in the manganese content. However, the upper limit for useful purposes appears to be 15% since the ductility at 600 F. is so low. The tensile properties obtained at 600 F. are considerably higher than those of the two commercial aluminum base alloys referred to hereinabove. It is also significant that the high strength at 600 F. was obtained without any preliminary thermal treatment of the worked powder products, such as a solution heat treatment, which is an economic advantage.
Having thus described our invention and certain embodiments thereof, we claim:
1. A hot worked aluminum base alloy powder article free from aluminum oxide except as an incidental im purity and having a maximum iron content of 1%, said hot worked alloy powder article being formed from atomized powder of an aluminum base alloy containing at least 70% by weight of aluminum and from 1.5 to 15% by weight of manganese as the essential component, the amount of said component exceeding the total quantity of any hardening elements present in the alloy, said alloy being substantially free from elements which form a solid solution with aluminum, except as they occur as impurities, said hot worked article being characterized in the as-worked condition by a tensile strength at 600 F. after a hour exposure of not less than 12,000 p.s.i. and a yield strength of not less than 10,000 p.s.i.
2. A hot worked aluminum base alloy powder article according to claim 1 wherein the manganese content is 5 to 10%.
3. A hot worked aluminum base alloy powder article according to claim 1 wherein the alloy also contains at least one hardening element selected from the group consisting of nickel, cobalt, chromium, titanium, vanadium, molybdenum, Zirconium and tungsten in amounts of 0.1 to 10% each by weight, the total not exceeding 10% by Weight, the manganese content of said alloy exceeding the total amount of hardening elements added thereto.
Jones June 23, 1942 Ennor Oct. 15, 1957

Claims (1)

1. A HOT WORKED ALUMINUM BASE ALLOY POWDER ARTICLE FREE FROM ALUMINUM OXIDE EXCEPT AS AN INCIDENTAL IMPURITY AND HAVING A MAXIMUM IRON CONTENT OF 1%, SAID HOT WORKED ALLOY POWDER ARTICLE BEING FORMED FROM ATOMIZED POWDER OF AN ALUMINUM BASE ALLOY CONTAINING AT LEAST 70% BY WEIGHT OF ALUMINUM AND FROM 1.5 TO 15% BY WEIGHT OF MANGANESE AS THE ESSENTIAL COMPONENT, THE AMOUNT OF SAID COMPONENT EXCEEDING THE TOTAL QUANTITY OF ANY HARDENING ELEMENTS PRESENT IN THE ALLOY, SAID ALLOY BEING SUBSTANTIALLY FREE FROM ELEMENTS WHICH FORM A SOLID SOLUTION WITH ALUMINUM, EXCEPT AS THEY OCCUR AS IMPURITIES, SAID HOT WORKED ARTICLE BEING CHARACTERIZED IN THE AS-WORKED CONDITION BY A TENSILE STRENGTH AT 600* F. AFTER A 100 HOUR EXPOSURE OF NOT LESS THAN 12,000 P.S.I. AND A YIELD STRENGTH OF NOT LESS THAN 10,000 P.S.I.
US724226A 1958-03-27 1958-03-27 Aluminum base alloy powder product Expired - Lifetime US2966731A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US724226A US2966731A (en) 1958-03-27 1958-03-27 Aluminum base alloy powder product

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US724226A US2966731A (en) 1958-03-27 1958-03-27 Aluminum base alloy powder product

Publications (1)

Publication Number Publication Date
US2966731A true US2966731A (en) 1961-01-03

Family

ID=24909558

Family Applications (1)

Application Number Title Priority Date Filing Date
US724226A Expired - Lifetime US2966731A (en) 1958-03-27 1958-03-27 Aluminum base alloy powder product

Country Status (1)

Country Link
US (1) US2966731A (en)

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3177073A (en) * 1962-03-26 1965-04-06 Dow Chemical Co High strength aluminum alloy for pellet extrusion and product
US3219491A (en) * 1962-07-13 1965-11-23 Aluminum Co Of America Thermal treatment of aluminum base alloy product
US3219492A (en) * 1962-11-16 1965-11-23 Aluminum Co Of America Thermal treatment of aluminum base alloy product
US3226267A (en) * 1962-03-26 1965-12-28 Dow Chemical Co High strength aluminum alloy extrusion process and product
US3236632A (en) * 1964-12-01 1966-02-22 Dow Chemical Co High strength aluminum alloy for pellet extrusion and product
US3265493A (en) * 1963-05-31 1966-08-09 Dow Chemical Co Aluminum base pellet alloys containing copper and magnesium and process for producing the same
US3386820A (en) * 1966-01-26 1968-06-04 Olin Mathieson Aluminum base alloy containing zirconium-chromium-manganese
US3462248A (en) * 1956-12-14 1969-08-19 Kaiser Aluminium Chem Corp Metallurgy
EP0137180A1 (en) * 1983-08-17 1985-04-17 Nissan Motor Co., Ltd. Heat-resisting aluminium alloy
US4715893A (en) * 1984-04-04 1987-12-29 Allied Corporation Aluminum-iron-vanadium alloys having high strength at elevated temperatures
US4743317A (en) * 1983-10-03 1988-05-10 Allied Corporation Aluminum-transition metal alloys having high strength at elevated temperatures
US4805686A (en) * 1983-10-03 1989-02-21 Allied-Signal Inc. An apparatus for forming aluminum-transition metal alloys having high strength at elevated temperatures
EP0304284A1 (en) * 1987-08-18 1989-02-22 Alcan International Limited Aluminum alloys and a method of production
US4832737A (en) * 1985-09-18 1989-05-23 Vereinigte Aluminium-Werke Aktiengesellschaft High temperature-resistant aluminum alloy and process for its production
US5174955A (en) * 1983-08-17 1992-12-29 Nissan Motor Co., Ltd. Heat-resisting aluminum alloy

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2287251A (en) * 1939-07-07 1942-06-23 Jones William David Manufacture of nonporous metal articles
US2809891A (en) * 1954-10-12 1957-10-15 Aluminum Co Of America Method of making articles from aluminous metal powder

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2287251A (en) * 1939-07-07 1942-06-23 Jones William David Manufacture of nonporous metal articles
US2809891A (en) * 1954-10-12 1957-10-15 Aluminum Co Of America Method of making articles from aluminous metal powder

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3462248A (en) * 1956-12-14 1969-08-19 Kaiser Aluminium Chem Corp Metallurgy
US3226267A (en) * 1962-03-26 1965-12-28 Dow Chemical Co High strength aluminum alloy extrusion process and product
US3177073A (en) * 1962-03-26 1965-04-06 Dow Chemical Co High strength aluminum alloy for pellet extrusion and product
US3219491A (en) * 1962-07-13 1965-11-23 Aluminum Co Of America Thermal treatment of aluminum base alloy product
US3219492A (en) * 1962-11-16 1965-11-23 Aluminum Co Of America Thermal treatment of aluminum base alloy product
US3265493A (en) * 1963-05-31 1966-08-09 Dow Chemical Co Aluminum base pellet alloys containing copper and magnesium and process for producing the same
US3236632A (en) * 1964-12-01 1966-02-22 Dow Chemical Co High strength aluminum alloy for pellet extrusion and product
US3386820A (en) * 1966-01-26 1968-06-04 Olin Mathieson Aluminum base alloy containing zirconium-chromium-manganese
EP0137180A1 (en) * 1983-08-17 1985-04-17 Nissan Motor Co., Ltd. Heat-resisting aluminium alloy
US5174955A (en) * 1983-08-17 1992-12-29 Nissan Motor Co., Ltd. Heat-resisting aluminum alloy
US4743317A (en) * 1983-10-03 1988-05-10 Allied Corporation Aluminum-transition metal alloys having high strength at elevated temperatures
US4805686A (en) * 1983-10-03 1989-02-21 Allied-Signal Inc. An apparatus for forming aluminum-transition metal alloys having high strength at elevated temperatures
US4715893A (en) * 1984-04-04 1987-12-29 Allied Corporation Aluminum-iron-vanadium alloys having high strength at elevated temperatures
US4832737A (en) * 1985-09-18 1989-05-23 Vereinigte Aluminium-Werke Aktiengesellschaft High temperature-resistant aluminum alloy and process for its production
EP0304284A1 (en) * 1987-08-18 1989-02-22 Alcan International Limited Aluminum alloys and a method of production

Similar Documents

Publication Publication Date Title
US2963780A (en) Aluminum alloy powder product
US2966731A (en) Aluminum base alloy powder product
US4379719A (en) Aluminum powder alloy product for high temperature application
US2966736A (en) Aluminum base alloy powder product
US4464199A (en) Aluminum powder alloy product for high temperature application
US2809891A (en) Method of making articles from aluminous metal powder
US3709667A (en) Dispersion strengthening of platinum group metals and alloys
US4888054A (en) Metal composites with fly ash incorporated therein and a process for producing the same
US3462248A (en) Metallurgy
US2966735A (en) Aluminum base alloy powder product
US4732610A (en) Al-Zn-Mg-Cu powder metallurgy alloy
US2966732A (en) Aluminum base alloy powder product
US3004331A (en) Aluminum base alloy powder product
US5384087A (en) Aluminum-silicon carbide composite and process for making the same
US4676830A (en) High strength material produced by consolidation of rapidly solidified aluminum alloy particulates
US3720551A (en) Method for making a dispersion strengthened alloy article
JPH0153342B2 (en)
US2994947A (en) Aluminum base alloy powder product
EP0668806B1 (en) Silicon alloy, method for producing the alloy and method for production of consolidated products from silicon alloy
US2966733A (en) Aluminum base alloy powder product
US2966734A (en) Aluminum base alloy powder product
US5833772A (en) Silicon alloy, method for producing the alloy and method for production of consolidated products from silicon
JPH0234740A (en) Heat-resistant aluminum alloy material and its manufacture
JPS5943802A (en) Aluminum-transition metal alloy from quick coagulating powder and manufacture
US2796660A (en) Method for the production of light metal articles