US2706680A - Aluminum base alloy - Google Patents

Aluminum base alloy Download PDF

Info

Publication number
US2706680A
US2706680A US273773A US27377352A US2706680A US 2706680 A US2706680 A US 2706680A US 273773 A US273773 A US 273773A US 27377352 A US27377352 A US 27377352A US 2706680 A US2706680 A US 2706680A
Authority
US
United States
Prior art keywords
alloy
manganese
copper
alloys
aluminum
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
US273773A
Inventor
Charles B Criner
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 US273773A priority Critical patent/US2706680A/en
Application granted granted Critical
Publication of US2706680A publication Critical patent/US2706680A/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
    • C22C21/00Alloys based on aluminium

Definitions

  • This invention is concerned with aluminum base alloys which are adapted for service at elevated temperatures, particularly such as required in certain parts of jet engines.
  • An object of the invention is to provide an aluminum base alloy composition that possesses a combination of high strength and a high resistance to creep and fatigue at elevated temperatures.
  • Aluminum base alloys have long been used for such parts of internal combustion engines as pistons, cylinder heads and connecting rods and they have served quite satisfactorily for these purposes. Typical of the alloys that have been used for these parts are those which, in addition to aluminum, contain 4% copper, 1.5% magnesium and 2% nickel; 10% copper, 1.25% iron and 0.25% magnesium; or, 12% silicon, 1.2% magnesium, 2.5% nickel and 0.8% copper. With the advent of more powerful motors and auxiliary equipment, especially jet engines, it has been found that the above alloys do not possess the requisite properties for long time operation. The requirements for compressor parts in jet engines, for example, have demanded the utmost from aluminum base alloys.
  • My invention is based on the discovery that a highly satisfactory combination of strength and resistance to fatigue and creep at high temperatures is to be found in a magnesium-free aluminum base alloy containing copper as the chief added component and small amounts of manganese, vanadium and zirconium. More specifically the alloy should consist essentially of aluminum, from to 13% copper, 0.15 to 1.7% manganese, 0.05 to .20% vanadium and 0.05 to 0.30% zirconium, the iron impurity not exceeding 0.75% and the silicon impurity being below 0.40%. Furthermore, the amount of manganese should be between 3 and 13% of the copper content. The presence of the small amount of manganese, vanadium and Zirconium considerably modifies the properties of the binary aluminum-copper alloy at elevated temperatures.
  • the alloy should contain no more than about 0.02% magnesium and hence it is here referred to as being magnesium-free.
  • the alloy should contain from 5 to 9% copper, 0.15 to 1.20% manganese, 0.05 to 0.15% vanadium and 0.05 to 0.25 zirconium, the silicon and iron impurities amounting to 0.05 to 0.30% silicon and 0.05 to 0.50% iron.
  • the amount of manganese should be between 3 and 13% of the copper content as indicated hereinabove. It is also desirable that the alloy be given both solution and precipitation hardening treatments to produce the maximum properties. Alloys within the foregoing range which have received the prescribed thermal treatment may be expected to have at 400 F. a tensile strength after hr. exposure of 39,000 p. s.
  • the alloys may be desirable to add 0.01 to 0.25% of one or more of the following elements: cobalt, nickel, molybdenum, tungsten, chromium, titanium, boron, tantalum and niobium, the total amount of such elements not exceeding 0.25%.
  • the thermal treatment that may be used to enhance the properties of my alloys should consist of heating them to a temperature between960 and 1000 F. for a period of 2 to 24 hours followed by quenching, preferably in water at 70 to F. The quenched alloys may then be reheated to 350 to 450 F. for a period of 1 to 50 hours.
  • My alloys may be used in the non-heat treated condition, if a maximum strength is not demanded, for even in that condition they represent an improvement over such well known alloys as one composed of aluminum, 4% copper, 1.5% magnesium and 2% nickel.
  • sand cast test bars of an aluminum, 6% copper, 0.3% manganese, 0.25% zirconium of 0.1% vanadium alloy had a tensile strength of 14,500 p. s. i., a yield strength of 9,600 p. s. i. and an elongation of 21% at 600 F.
  • the foregoing aluminum-copper-magnesium-nickel composition has a typical tensile strength of but 8,000 p. s. i. and a yield strength of 6,000 p. s. i. at 600 F.
  • the minimum creep rate values mentioned herein were obtained in the following manner. Standard /2 in. diameter bars were placed in small electrically heated air furnace and maintained under a constant load throughout the period of the test by means of a dead weight and lever system. The furnace temperature was automatically controlled. Measurements of extension or creep were made at regular intervals throughout the test period to the nearest 0.000005 in. To obtain the minimum creep rate, the measured values of creep were plotted against time on Cartesian coordinates and the minimum slope of the resulting curve determined. The minimum creep rate thus determined is also known as the secondary creep rate.
  • Stresses for specific creep rates were determined in customary manner from graphs in which the creep rates mentioned above were plotted logarithmically against stress. Stress rupture values were obtained in a similar manner by determining the time required for rupture at a given stress for each of several specimens under different stresses. By interpolation in the customary manner specific stresses were found which would be expected to cause rupture in specific times.
  • the alloys of my invention may be used in the cast state or they may be worked. This is of practical importance since it may be possible to use a single composition for both cast and wrought products.
  • a magnesium-free aluminum base alloy consisting of aluminum, 5 to 13% copper, 0.15 to 1.7% manganese, 0.05 to 0.20% vanadium, 0.05 to 0.30% zirconium, and 0.01 to 0.25% of at least one of the elements of the group consisting of cobalt, nickel, molybdenum, tungsten, chromium, titanium, boron, tantalum and niobium, the total amount of said elements of said group not exceeding 0.25% the iron impurity in the alloy not exceeding 0.75%, and the silicon impurity being not over 0.40%, the amount of manganese being between 3 and 13% of the copper content.
  • a magnesium-free aluminum base alloy consisting essentially of aluminum, 5 to 13% copper, 0.15 to 1.7% manganese, 0.05 to 0.20% vanadium, and 0.05 to 0.30% zirconium, the iron impurity in the alloy not exceeding 0.75% and the silicon impurity being not over 0.40%, the amount of manganese being between 3 and 13% of the copper content, said alloy having a higher tensile strength and resistance to creep at elevated temperatures, on the order of 400 and 600 F., than the same alloy devoid of said manganese, vanadium and zirconium components.
  • a magnesium-free aluminum base alloy consisting essentially of aluminum, 5 to 9% copper, 0.15 to 1.20% manganese, 0.05 to 0.15% vanadium and 0.05 to 0.25 zirconium, the iron impurity in the alloy not exceeding 0.50% and the silicon impurity being not over 0.30%, the amount of manganese being between 3 and 13% of the copper content, said alloy having a higher tensile strength and resistance to creep at elevated temperatures, on the order of 400 and 600 F., than the same alloy devoid of said manganese, vanadium and zirconium components.
  • a solution heat treated and precipitation hardened magnesium-free aluminum base alloy consisting essentially of aluminum, 5 to 13% copper, 0.15 to 1.7% manganese, 0.05 to 0.20% vanadium and 0.05 to 0.30% zirconium, the iron impurity in the alloy not exceeding 0.75% and the silicon impurity being not over 0.40%, the amount of manganese being between 3 and 13% of the copper content, said alloy having the internal structure developed by a solution heat treatment at 960 to 1000 F. for a period of 2 to 24 hours and a precipitation hardening treatment at 350 to 450 F.
  • said solution heat treated and precipitation hardened alloy having a higher tensile strength and resistance to creep at elevated temperatures, on the order of 400 and 600 F., than the same alloy devoid of said manganese, vanadium and zirconium components.

Description

United States Patent ALUMINUM BASE ALLOY Charles B. Criner, New Kensington, Pa., assignor to Aluminum Company of America, Pittsburgh, Pa., a corporation of Pennsylvania No Drawing. Application February 27, 1952, Serial No. 273,773
4 Claims. (Cl. 75-139) This invention is concerned with aluminum base alloys which are adapted for service at elevated temperatures, particularly such as required in certain parts of jet engines. An object of the invention is to provide an aluminum base alloy composition that possesses a combination of high strength and a high resistance to creep and fatigue at elevated temperatures.
Aluminum base alloys have long been used for such parts of internal combustion engines as pistons, cylinder heads and connecting rods and they have served quite satisfactorily for these purposes. Typical of the alloys that have been used for these parts are those which, in addition to aluminum, contain 4% copper, 1.5% magnesium and 2% nickel; 10% copper, 1.25% iron and 0.25% magnesium; or, 12% silicon, 1.2% magnesium, 2.5% nickel and 0.8% copper. With the advent of more powerful motors and auxiliary equipment, especially jet engines, it has been found that the above alloys do not possess the requisite properties for long time operation. The requirements for compressor parts in jet engines, for example, have demanded the utmost from aluminum base alloys. It has been learned that while some alloys may have a satisfactory strength at elevated temperatures their resistance to creep and fatigue are so low as to make them unacceptable. In other cases the alloys may have interesting properties at high temperatures but they are so difficult to cast and work as to remove them from consideration as practical materials.
Effort has therefore been made to find an alloy which would possess both high strength and high resistance to creep and fatigue and still be amenable to fabrication by conventional methods.
My invention is based on the discovery that a highly satisfactory combination of strength and resistance to fatigue and creep at high temperatures is to be found in a magnesium-free aluminum base alloy containing copper as the chief added component and small amounts of manganese, vanadium and zirconium. More specifically the alloy should consist essentially of aluminum, from to 13% copper, 0.15 to 1.7% manganese, 0.05 to .20% vanadium and 0.05 to 0.30% zirconium, the iron impurity not exceeding 0.75% and the silicon impurity being below 0.40%. Furthermore, the amount of manganese should be between 3 and 13% of the copper content. The presence of the small amount of manganese, vanadium and Zirconium considerably modifies the properties of the binary aluminum-copper alloy at elevated temperatures. The precise manner in which these elements cooperate with each other and with the copper component is not understood but it has been found that the foregoing limits must be strictly observed to obtain the desired results. While the alloy exhibits improved properties in both the cast and worked conditions the improvement is more clearly evident where it receives a solution heat treatment with or without subsequent precipitation hardening treatment. The use of a solution heat treatment has the further advantage of homogenizing the alloy and insuring a more uniform product.
The alloy should contain no more than about 0.02% magnesium and hence it is here referred to as being magnesium-free.
For optimum results the alloy should contain from 5 to 9% copper, 0.15 to 1.20% manganese, 0.05 to 0.15% vanadium and 0.05 to 0.25 zirconium, the silicon and iron impurities amounting to 0.05 to 0.30% silicon and 0.05 to 0.50% iron. The amount of manganese, of course, should be between 3 and 13% of the copper content as indicated hereinabove. It is also desirable that the alloy be given both solution and precipitation hardening treatments to produce the maximum properties. Alloys within the foregoing range which have received the prescribed thermal treatment may be expected to have at 400 F. a tensile strength after hr. exposure of 39,000 p. s. i., a minimum creep rate of on the order of 0.00006 to 0.00016 in./in./hr. under a stress of 25,000 p. s. i., a stress for rupture in 1000 hours of 23,000 p. s. i. and to not fail in fatigue at a stress of 13000 p. s. i. in less than about 20 million cycles.
To obtain a finer grain size or enhance minor characteristics of the alloys it may be desirable to add 0.01 to 0.25% of one or more of the following elements: cobalt, nickel, molybdenum, tungsten, chromium, titanium, boron, tantalum and niobium, the total amount of such elements not exceeding 0.25%.
The thermal treatment that may be used to enhance the properties of my alloys should consist of heating them to a temperature between960 and 1000 F. for a period of 2 to 24 hours followed by quenching, preferably in water at 70 to F. The quenched alloys may then be reheated to 350 to 450 F. for a period of 1 to 50 hours.
My alloys may be used in the non-heat treated condition, if a maximum strength is not demanded, for even in that condition they represent an improvement over such well known alloys as one composed of aluminum, 4% copper, 1.5% magnesium and 2% nickel. For example, sand cast test bars of an aluminum, 6% copper, 0.3% manganese, 0.25% zirconium of 0.1% vanadium alloy had a tensile strength of 14,500 p. s. i., a yield strength of 9,600 p. s. i. and an elongation of 21% at 600 F. whereas the foregoing aluminum-copper-magnesium-nickel composition has a typical tensile strength of but 8,000 p. s. i. and a yield strength of 6,000 p. s. i. at 600 F.
The minimum creep rate values mentioned herein were obtained in the following manner. Standard /2 in. diameter bars were placed in small electrically heated air furnace and maintained under a constant load throughout the period of the test by means of a dead weight and lever system. The furnace temperature was automatically controlled. Measurements of extension or creep were made at regular intervals throughout the test period to the nearest 0.000005 in. To obtain the minimum creep rate, the measured values of creep were plotted against time on Cartesian coordinates and the minimum slope of the resulting curve determined. The minimum creep rate thus determined is also known as the secondary creep rate.
Stresses for specific creep rates were determined in customary manner from graphs in which the creep rates mentioned above were plotted logarithmically against stress. Stress rupture values were obtained in a similar manner by determining the time required for rupture at a given stress for each of several specimens under different stresses. By interpolation in the customary manner specific stresses were found which would be expected to cause rupture in specific times.
The alloys of my invention may be used in the cast state or they may be worked. This is of practical importance since it may be possible to use a single composition for both cast and wrought products.
The properties of cast and forged alloys made in accordance with my invention and one not so made are illustrated in the following examples. The alloys had the compositions given in the table below:
Alloy On 'Mn V Zr Fe Si Others Forged 1" sq. bars of alloys A, B, C, and D were given a solution heat treatment at 1000 F. for a period of 1 or 2 hours, followed by quenching in water and precipitation hardening at 375 F. for 12 hours. Castto-size test bars of alloy E were heat treated at 985 F., quenched and precipitation hardened by heating at 375 F. for 12 hours. Samples of the forged bars were heated to a temperature of 600 F. for a period of 100 hours, while the cast bars were heated to the same temperature for 48 hours and their tensile and yield strengths determined at that temperature. The tensile values obtained under this condition are given in Table II below:
Comparing the values for alloys A, B and C with D it is apparent that the presence of manganese has an important effect upon the strength of the alloy for in its absence the tensile and yield strengths are considerably reduced. Also, the strength of the cast bars of alloy E is higher than that of the forged bars.
Typical values for the minimum creep rate and stress for rupture at 400 and 600 F. of forged, solution heat treated, quenched and precipitation hardened test bars of an alloy having a nominal composition of 6% copper, 0.3% manganese, 0.10% vanadium, 0.25% zirconium and balance aluminum plus impurities are given in Tables III and IV below:
TABLE III Creep characteristics at 400 and 600 F.
The fatigue values for tests at 400 F. on solution heat treated, quenched and precipitation hardened forged test bars of alloy A are given in Table V below:
4 TABLE v Fatigue test results at 400 F.
Millions of Cycles for Failure at Stress of- 12, 000 13, 000 17, 00 p. s. i. p. s. i. p. i.
Having described my invention and certain embodiments thereof I claim:
1. A magnesium-free aluminum base alloy consisting of aluminum, 5 to 13% copper, 0.15 to 1.7% manganese, 0.05 to 0.20% vanadium, 0.05 to 0.30% zirconium, and 0.01 to 0.25% of at least one of the elements of the group consisting of cobalt, nickel, molybdenum, tungsten, chromium, titanium, boron, tantalum and niobium, the total amount of said elements of said group not exceeding 0.25% the iron impurity in the alloy not exceeding 0.75%, and the silicon impurity being not over 0.40%, the amount of manganese being between 3 and 13% of the copper content.
2. A magnesium-free aluminum base alloy consisting essentially of aluminum, 5 to 13% copper, 0.15 to 1.7% manganese, 0.05 to 0.20% vanadium, and 0.05 to 0.30% zirconium, the iron impurity in the alloy not exceeding 0.75% and the silicon impurity being not over 0.40%, the amount of manganese being between 3 and 13% of the copper content, said alloy having a higher tensile strength and resistance to creep at elevated temperatures, on the order of 400 and 600 F., than the same alloy devoid of said manganese, vanadium and zirconium components.
3. A magnesium-free aluminum base alloy consisting essentially of aluminum, 5 to 9% copper, 0.15 to 1.20% manganese, 0.05 to 0.15% vanadium and 0.05 to 0.25 zirconium, the iron impurity in the alloy not exceeding 0.50% and the silicon impurity being not over 0.30%, the amount of manganese being between 3 and 13% of the copper content, said alloy having a higher tensile strength and resistance to creep at elevated temperatures, on the order of 400 and 600 F., than the same alloy devoid of said manganese, vanadium and zirconium components.
4. A solution heat treated and precipitation hardened magnesium-free aluminum base alloy consisting essentially of aluminum, 5 to 13% copper, 0.15 to 1.7% manganese, 0.05 to 0.20% vanadium and 0.05 to 0.30% zirconium, the iron impurity in the alloy not exceeding 0.75% and the silicon impurity being not over 0.40%, the amount of manganese being between 3 and 13% of the copper content, said alloy having the internal structure developed by a solution heat treatment at 960 to 1000 F. for a period of 2 to 24 hours and a precipitation hardening treatment at 350 to 450 F. for a period of 1 to 50 hours, said solution heat treated and precipitation hardened alloy having a higher tensile strength and resistance to creep at elevated temperatures, on the order of 400 and 600 F., than the same alloy devoid of said manganese, vanadium and zirconium components.
References Cited in the file of this patent UNITED STATES PATENTS 2,047,873 Kempf-Dean July 14, 1936 2,225,925 Nock Dec. 24, 1940 2,459,492 Bradbury Jan. 18, 1949 FOREIGN PATENTS 596,178 Great Britain Dec. 30, 1947

Claims (1)

  1. 2. A MAGNESIUM-FREE ALUMINUM BASE ALLOY CONSISTING ESSENTIALLY OF ALUMINUM, 5 TO 13% COPPER, 0.15 TO 1.7% MANGANESE, 0.05 TO 0.02% VANADIUM, AND 0.05 TO 0.30% ZIRCONIUM, THE IRON IMPURITY IN THE ALLOY NOT EXCEEDING 0.75% AND THE SILICON IMPURITY BEING NOT OVER 0.40%, THE AMOUNT OF MANGANESE BEING BETWEEN 3 AND 13% OF THE COPPER CONTENT, SAID ALLOY HAVING A HIGHER TENSILE STRENGHT AND RESISTANCE TO CREEP AT ELEVATED TEMPERATURE ON THE ORDER OF 400 AND 600* F., THAN THE SAME ALLOY DEVOID OF SAID MANGANESE, VANDIUM AND ZIRCONIUM COMPONENTS.
US273773A 1952-02-27 1952-02-27 Aluminum base alloy Expired - Lifetime US2706680A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US273773A US2706680A (en) 1952-02-27 1952-02-27 Aluminum base alloy

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US273773A US2706680A (en) 1952-02-27 1952-02-27 Aluminum base alloy

Publications (1)

Publication Number Publication Date
US2706680A true US2706680A (en) 1955-04-19

Family

ID=23045334

Family Applications (1)

Application Number Title Priority Date Filing Date
US273773A Expired - Lifetime US2706680A (en) 1952-02-27 1952-02-27 Aluminum base alloy

Country Status (1)

Country Link
US (1) US2706680A (en)

Cited By (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2784126A (en) * 1953-04-22 1957-03-05 Aluminum Co Of America Aluminum base alloy
DE1118473B (en) * 1958-05-21 1961-11-30 Kurt Dies Dr Ing Use of tempered aluminum cast alloys as a material for rail vehicle wheels with a shrunk-on steel wheel rim
US3253965A (en) * 1963-09-11 1966-05-31 Aluminum Co Of America Thermal treatment of aluminum base alloy articles
US3282745A (en) * 1963-05-27 1966-11-01 Dow Chemical Co High strength fabrications of aluminum base alloys containing copper
US3307978A (en) * 1964-02-17 1967-03-07 Dow Chemical Co Process for preparing high strength fabricated articles from aluminum-base alloys containing copper
US3725309A (en) * 1969-01-15 1973-04-03 Ibm Copper doped aluminum conductive stripes
EP0485068A1 (en) * 1990-11-08 1992-05-13 Ford Motor Company Limited Aluminum casting alloy
US6368427B1 (en) 1999-09-10 2002-04-09 Geoffrey K. Sigworth Method for grain refinement of high strength aluminum casting alloys
US20060133949A1 (en) * 2003-07-10 2006-06-22 Gerard Laslaz Moulded AL-SI-CU aluminium alloy component with high hot-process resistance
US20070102071A1 (en) * 2005-11-09 2007-05-10 Bac Of Virginia, Llc High strength, high toughness, weldable, ballistic quality, castable aluminum alloy, heat treatment for same and articles produced from same
EP2097551A1 (en) * 2006-12-13 2009-09-09 Hydro Aluminium As Aluminium casting alloy, method for the manufacture of a casting and cast component for combustion engines
DE102011014590A1 (en) * 2011-01-27 2012-08-02 Volkswagen Aktiengesellschaft Preparation of aluminum alloy for manufacturing aluminum cast, involves alloying base alloy containing aluminum, copper and titanium, adding zirconium and alloying
US20150368772A1 (en) * 2014-06-19 2015-12-24 Apple Inc. Aluminum Alloys with Anodization Mirror Quality
US20160362769A1 (en) * 2015-06-12 2016-12-15 Hamilton Sundstrand Corporation Particulate for additive manufacturing techniques
US20180327890A1 (en) * 2017-05-12 2018-11-15 Ut-Battelle, Llc Aluminum alloy compositions and methods of making and using the same
US10208371B2 (en) 2016-07-13 2019-02-19 Apple Inc. Aluminum alloys with high strength and cosmetic appeal
US10597762B2 (en) 2013-09-30 2020-03-24 Apple Inc. Aluminum alloys with high strength and cosmetic appeal
US20210285077A1 (en) * 2020-03-04 2021-09-16 Amit Shyam High temperature cast aluminum-copper-manganese-zirconium alloys with low temperature ductility
TWI741962B (en) * 2021-04-16 2021-10-01 圓融金屬粉末股份有限公司 Aluminum-nickel-copper alloy and manufacturing method thereof
US11180839B2 (en) 2017-10-26 2021-11-23 Ut-Battelle, Llc Heat treatments for high temperature cast aluminum alloys
US11220729B2 (en) * 2016-05-20 2022-01-11 Ut-Battelle, Llc Aluminum alloy compositions and methods of making and using the same
US11345980B2 (en) 2018-08-09 2022-05-31 Apple Inc. Recycled aluminum alloys from manufacturing scrap with cosmetic appeal

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2047873A (en) * 1935-12-03 1936-07-14 Aluminum Co Of America Free cutting alloys
US2225925A (en) * 1936-12-15 1940-12-24 Aluminum Co Of America Heat treated alloy
GB596178A (en) * 1945-07-24 1947-12-30 Tennyson Fraser Bradbury Aluminium base alloys
US2459492A (en) * 1944-02-25 1949-01-18 Rolls Royce Aluminum copper alloy

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2047873A (en) * 1935-12-03 1936-07-14 Aluminum Co Of America Free cutting alloys
US2225925A (en) * 1936-12-15 1940-12-24 Aluminum Co Of America Heat treated alloy
US2459492A (en) * 1944-02-25 1949-01-18 Rolls Royce Aluminum copper alloy
GB596178A (en) * 1945-07-24 1947-12-30 Tennyson Fraser Bradbury Aluminium base alloys

Cited By (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2784126A (en) * 1953-04-22 1957-03-05 Aluminum Co Of America Aluminum base alloy
DE1118473B (en) * 1958-05-21 1961-11-30 Kurt Dies Dr Ing Use of tempered aluminum cast alloys as a material for rail vehicle wheels with a shrunk-on steel wheel rim
US3282745A (en) * 1963-05-27 1966-11-01 Dow Chemical Co High strength fabrications of aluminum base alloys containing copper
US3253965A (en) * 1963-09-11 1966-05-31 Aluminum Co Of America Thermal treatment of aluminum base alloy articles
US3307978A (en) * 1964-02-17 1967-03-07 Dow Chemical Co Process for preparing high strength fabricated articles from aluminum-base alloys containing copper
US3725309A (en) * 1969-01-15 1973-04-03 Ibm Copper doped aluminum conductive stripes
EP0485068A1 (en) * 1990-11-08 1992-05-13 Ford Motor Company Limited Aluminum casting alloy
US5120372A (en) * 1990-11-08 1992-06-09 Ford Motor Company Aluminum casting alloy for high strength/high temperature applications
US6368427B1 (en) 1999-09-10 2002-04-09 Geoffrey K. Sigworth Method for grain refinement of high strength aluminum casting alloys
US20060133949A1 (en) * 2003-07-10 2006-06-22 Gerard Laslaz Moulded AL-SI-CU aluminium alloy component with high hot-process resistance
US20070102071A1 (en) * 2005-11-09 2007-05-10 Bac Of Virginia, Llc High strength, high toughness, weldable, ballistic quality, castable aluminum alloy, heat treatment for same and articles produced from same
EP2097551A4 (en) * 2006-12-13 2010-09-22 Hydro Aluminium As Aluminium casting alloy, method for the manufacture of a casting and cast component for combustion engines
EP2097551A1 (en) * 2006-12-13 2009-09-09 Hydro Aluminium As Aluminium casting alloy, method for the manufacture of a casting and cast component for combustion engines
DE102011014590A1 (en) * 2011-01-27 2012-08-02 Volkswagen Aktiengesellschaft Preparation of aluminum alloy for manufacturing aluminum cast, involves alloying base alloy containing aluminum, copper and titanium, adding zirconium and alloying
DE102011014590A8 (en) * 2011-01-27 2013-01-17 Volkswagen Aktiengesellschaft A method of producing an aluminum alloy, an aluminum alloy, and a method of manufacturing an aluminum cast member and an aluminum casting member
US10597762B2 (en) 2013-09-30 2020-03-24 Apple Inc. Aluminum alloys with high strength and cosmetic appeal
US20150368772A1 (en) * 2014-06-19 2015-12-24 Apple Inc. Aluminum Alloys with Anodization Mirror Quality
US20160362769A1 (en) * 2015-06-12 2016-12-15 Hamilton Sundstrand Corporation Particulate for additive manufacturing techniques
US11220729B2 (en) * 2016-05-20 2022-01-11 Ut-Battelle, Llc Aluminum alloy compositions and methods of making and using the same
US10208371B2 (en) 2016-07-13 2019-02-19 Apple Inc. Aluminum alloys with high strength and cosmetic appeal
US10544493B2 (en) 2016-07-13 2020-01-28 Apple Inc. Aluminum alloys with high strength and cosmetic appeal
US20180327890A1 (en) * 2017-05-12 2018-11-15 Ut-Battelle, Llc Aluminum alloy compositions and methods of making and using the same
US11242587B2 (en) * 2017-05-12 2022-02-08 Ut-Battelle, Llc Aluminum alloy compositions and methods of making and using the same
US11180839B2 (en) 2017-10-26 2021-11-23 Ut-Battelle, Llc Heat treatments for high temperature cast aluminum alloys
US11345980B2 (en) 2018-08-09 2022-05-31 Apple Inc. Recycled aluminum alloys from manufacturing scrap with cosmetic appeal
US20210285077A1 (en) * 2020-03-04 2021-09-16 Amit Shyam High temperature cast aluminum-copper-manganese-zirconium alloys with low temperature ductility
TWI741962B (en) * 2021-04-16 2021-10-01 圓融金屬粉末股份有限公司 Aluminum-nickel-copper alloy and manufacturing method thereof

Similar Documents

Publication Publication Date Title
US2706680A (en) Aluminum base alloy
JP4861651B2 (en) Advanced Ni-Cr-Co alloy for gas turbine engines
US3160500A (en) Matrix-stiffened alloy
US4477292A (en) Three-step aging to obtain high strength and corrosion resistance in Al-Zn-Mg-Cu alloys
US2784126A (en) Aluminum base alloy
US2915390A (en) Aluminum base alloy
US3973952A (en) Heat resistant alloy casting
US2397034A (en) Heat-resisting alloys containing cobalt
US1947121A (en) Aluminum base alloys
US2829048A (en) High damping alloy and members prepared therefrom
US2486576A (en) Heat-treatment of cobalt base alloys and products
US2766156A (en) Heat-treatment of nickel-chromiumcobalt alloys
US3145124A (en) Heat treatment of nickel chromiumcobalt alloys
US3094414A (en) Nickel-chromium alloy
US3069258A (en) Nickel-chromium casting alloy with niobides
US2981620A (en) Cobalt-nickel base alloy
US3171760A (en) Thermal treatment of aluminum base alloy products
US6610155B2 (en) Aging treatment for Ni-Cr-Mo alloys
US2022686A (en) Aluminum alloy casting and method of making the same
US2968550A (en) Gall resistant nickel-copper alloy
US3107999A (en) Creep-resistant nickel-chromiumcobalt alloy
US2286627A (en) Aluminum base alloy
US3047381A (en) High temperature heat and creep resistant alloy
US2842439A (en) High strength alloy for use at elevated temperatures
US3110587A (en) Nickel-chromium base alloy