WO1991017281A1 - Double aged rapidly solidified aluminum-lithium alloys - Google Patents
Double aged rapidly solidified aluminum-lithium alloys Download PDFInfo
- Publication number
- WO1991017281A1 WO1991017281A1 PCT/US1991/000549 US9100549W WO9117281A1 WO 1991017281 A1 WO1991017281 A1 WO 1991017281A1 US 9100549 W US9100549 W US 9100549W WO 9117281 A1 WO9117281 A1 WO 9117281A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- component
- aluminum
- lithium
- mpa
- ranges
- Prior art date
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22F—CHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
- C22F1/00—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
- C22F1/04—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon
- C22F1/047—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon of alloys with magnesium as the next major constituent
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C21/00—Alloys based on aluminium
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22F—CHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
- C22F1/00—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
- C22F1/04—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22F—CHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
- C22F1/00—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
- C22F1/04—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon
- C22F1/057—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon of alloys with copper as the next major constituent
Definitions
- Double aged rapidly solidified aluminium-lithium alloys Double aged rapidly solidified aluminium-lithium alloys.
- the invention relates to rapidly solidified aluminum-lithium-copper-magnesium-zirconium powder metallurgy components having a combination of high ductility and high tensile strength; and more particularly to a process wherein the components are subjected to thermal treatment which improves yield and ultimate strengths thereof with minimal loss in tensile ductility.
- aluminum-lithium alloys derive strength and toughness through the formation of several precipitate phases, which are described in detail in the Conference Proceedings of Aluminum-Lithium V, edited by T.H. Sanders and E.A. Starke, pub. MCE, (1989).
- An important strengthening precipitate in . aluminum-lithium alloys is the metastable ⁇ phase which has a well defined solvus line.
- aluminum-lithium alloys are heat treatable, their strength increasing as ⁇ ' homogeneously nucleates from the supersaturated aluminum matrix.
- the ⁇ * phase consists of the ordered Ll 2 crystal structure and the composition Al 3 Li.
- the phase has a very small lattice misfit with the surrounding aluminum matrix and thus a coherent interface with the matrix. Dislocations easily shear the precipitates during deformation, resulting in the buildup of planar slip bands. This, in turn, reduces the toughness of aluminum lithium alloys. In binary aluminum-lithium alloys where this is the only strengthening phase employed, the slip planarity results in reduced toughness.
- the addition of copper and magnesium to aluminum-lithium alloys has two beneficial effects.
- the elements reduce the solubility of lithium in aluminum, increasing the amount of strengthening precipitates available.
- the copper and magnesium allow the formation of additional precipitate phases, most importantly the orthorhombic S' phase (Al 2 MgLi) and the hexagonal T 1 phase (Al 2 CuLi) .
- these phases are resistant to shearing by dislocations and are effective in minimizing slip planarity.
- the resulting homogeneity of the deformation results in improved toughness, increasing the applicability of these alloys over binary aluminum-lithium.
- these phases form sluggishly, precipitating primarily on heterogeneous nucleation sites such as dislocations.
- the alloys In order to generate these nucleations sites, the alloys must be cold worked prior to aging. Zirconium, at levels under approximately 0.15 wt%, is typically added to the alloys to form the etastable Al 3 Zr phase for grain size control and to retard recrystallization. Metastable Al 3 Zr consists of an Ll 2 crystal structure which is essentially isostructural with ⁇ ' (Al 3 Li) . Additions of zirconium to aluminum beyond 0.15 wt% using conventional casting practice result in the formation of relatively large dispersoids of equilibrium Al 3 Zr having the tetragonal D0 23 structure which are detrimental to toughness.
- the invention provides a method for increasing the tensile strength of a component composed of a rapidly solidified aluminum-lithium-copper-magnesium-zirconium alloy by subjecting the component to a multi-step aging treatment.
- the component is a consolidated article, formed from an alloy that is rapidly solidified and consists essentially of the formula Al bal Li a Cu tr Mg c Zr d wherein "a” ranges from about 2.1 to 3.4 wt%, “b” ranges from 0.5 to 2.0 wt%, “c” ranges from 0.2 to 2.0 wt%, and “d” ranges from about 0.4 to 1.8 wt%, the balance being aluminum.
- the aging treatment to which the component is subjected comprises the steps of subjecting the component to a preliminary aging treatment at a temperature of about 400°C-500°C for a time period ranging from about 0.5 to 10 hours; quenching the component in a fluid bath; and subjecting the component to a final aging treatment at a temperature of about 100°C-250°C for a time period ranging up to about 40 hours.
- the invention provides a component consolidated from a rapidly solidified aluminum-lithium alloy of the type delineated, which component has been subjected to the multi-step aging treatment specified hereinabove.
- FIG. 1 is a graph depicting the heat evolution/absorption vs. temperature as measured by differential scanning calorimetry for an Al-2.6Li-l.0Cu-0.5Mg-l.0Zr alloy aged at 590 ⁇ C for 2 hours and ice water quenched;
- FIG. 2 is a graph of the yield strength vs. aging temperature of a transverse specimen cut from an extruded bar aged for 2 hrs. followed by an ice water quench and subsequent aging for 16 hrs.
- the open rectangle providing data for a transverse specimen cut from an Al-2.34Li-l.07Zr extruded bar; the specimen being aged at 500°C for 1 hr. was water quenched and subsequently aged at 190°C for 2 hours;
- FIG. 3 is a graph of the ultimate tensile strength vs. aging temperature for specimens aged in the manner of the specimens of Fig. 2;
- FIG. 4 is a graph of the tensile elongation vs. aging temperature for specimens aged in the manner of the specimens of Fig. 2;
- FIG. 5 is a graph depicting the ultimate strength vs. elongation for the alloys of Fi ⁇ . 2 illustrating the improvement in properties extant along the diagonal away from the origin.
- the invention provides a thermal treatment that increases the tensile strength of a low density rapidly solidified aluminum-base alloy, consisting essentially of the formula wherein "a” ranges from 2.1 to 3.4 wt%, “b” ranges from about 0.5 to 2.0 wt%, “c” ranges from 0.2 to 2.0 wt%, “d M ranges from about 0.4 to 1.8 wt% and the balance is aluminum.
- the compacted alloy or component is subjected to a preliminary thermal treatment at temperatures ranging from about 400°C to 500 ⁇ C for a period of approximately 0.5 to 10 hours.
- this treatment dissolves elements such as Cu, Mg, and Li which may be microsegregated in precipitated phases such as ⁇ ' , ⁇ , T, and S.
- the thermal treatment produces an optimized distribution of cubic Ll 2 particles ranging from about 5 to 50 nanometers in size.
- the alloy article is then quenched in a fluid bath, preferably held between 0° and 60 ⁇ C.
- preliminary aging is intended to define the thermal treatment described in the first sentence of this paragraph.
- the compacted article is then aged at a temperature ranging from about 100°C to 250°C. for a time period ranging up to about 40 hours to provide selected strength/toughness tempers. No cold deformation step is required during this thermal processing, with the result that complex shaped components such as forgings produced from the aged component have excellent mechanical properties.
- Preliminary aging below approximately 400°C results in a deleterious drop in tensile properties due to the formation of undesirable phases such as the ⁇ (AlLi) phase.
- Preliminary aging above approximately 500 ⁇ C results in an acceptable combination of tensile properties but does not result in the attainment of the optimum tensile strength since the volume fraction of precipitates is reduced. Grain coarsening may also occur at temperature beyond 550 ⁇ C, further reducing strength.
- Consolidated articles aged in accordance with the invention exhibit tensile yield strength ranging from about 400 MPa (58 ksi) to 545 MPa (79 ksi) , ultimate tensile strength ranging from about 510 MPa (74ksi) to MPa (83 ksi) and elongation to fracture ranging from about 4 to 9 % when measured at room temperature (20°C) .
- the tensile properties of consolidated articles formed by extrusion of the alloys listed in Table I and thermally processed in accordance with the method of the invention are listed in Table II.
- the extruded bars were given a preliminary age for 2 hours at temperatures between 400°C and 600°C and quenched into an ice water bath; subsequently, they were aged at 135°C for 16 hours.
- Transverse specimens were then cut and machined into round tensile specimens having a gauge diameter of 3/8 - 8 - inches and a gauge length of 3/4 inches.
- Tensile testing was performed at room temperature at a strain rate of 5.5x10 -4 sec _1
- Figures 2, 3, and 4 are graphs of the data listed in Table II.
- the graphs illustrate that the peak ultimate tensile strength (UTS) is a function of both zirconium content and temperature of the first aging treatment.
- UTS peak ultimate tensile strength
- a peak UTS of 570 MPa is obtained for 440°C preliminary aged Al-2.6Li-l.Cu-0.5Mg-l.0Zr while a peak UTS of 540 MPa is obtained for a 490°C preliminary aged Al-2.6Li-l.0Mg-0.6Zr.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Forging (AREA)
- Continuous Casting (AREA)
- Lens Barrels (AREA)
Abstract
Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP91507111A JPH05506271A (en) | 1990-05-02 | 1991-01-25 | Increasing the strength of rapidly solidified aluminum-lithium through double aging |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US51777490A | 1990-05-02 | 1990-05-02 | |
US517,774 | 1990-05-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1991017281A1 true WO1991017281A1 (en) | 1991-11-14 |
Family
ID=24061176
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1991/000549 WO1991017281A1 (en) | 1990-05-02 | 1991-01-25 | Double aged rapidly solidified aluminum-lithium alloys |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0528811A1 (en) |
JP (1) | JPH05506271A (en) |
AU (1) | AU7582291A (en) |
CA (1) | CA2079327A1 (en) |
WO (1) | WO1991017281A1 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1993008314A1 (en) * | 1991-10-25 | 1993-04-29 | Allied-Signal Inc. | Strength enhancement of rapidly solidified aluminum-lithium through double aging |
WO1993017138A1 (en) * | 1992-02-20 | 1993-09-02 | Allied-Signal Inc. | Rapidly solidified aluminum lithium alloys having zirconium for aircraft landing wheel applications |
WO1996018752A1 (en) * | 1994-12-10 | 1996-06-20 | British Aerospace Public Limited Company | Heat treatment of aluminium-lithium alloys |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1987003011A1 (en) * | 1985-11-19 | 1987-05-21 | Aluminum Company Of America | Aluminum-lithium alloys and method of making the same |
US4721537A (en) * | 1985-10-15 | 1988-01-26 | Rockwell International Corporation | Method of producing a fine grain aluminum alloy using three axes deformation |
US4747884A (en) * | 1985-04-03 | 1988-05-31 | Massachusetts Institute Of Technology | High strength aluminum-base alloy containing lithium and zirconium and methods of preparation |
-
1991
- 1991-01-25 WO PCT/US1991/000549 patent/WO1991017281A1/en not_active Application Discontinuation
- 1991-01-25 EP EP19910906823 patent/EP0528811A1/en not_active Ceased
- 1991-01-25 JP JP91507111A patent/JPH05506271A/en active Pending
- 1991-01-25 CA CA 2079327 patent/CA2079327A1/en not_active Abandoned
- 1991-01-25 AU AU75822/91A patent/AU7582291A/en not_active Abandoned
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4747884A (en) * | 1985-04-03 | 1988-05-31 | Massachusetts Institute Of Technology | High strength aluminum-base alloy containing lithium and zirconium and methods of preparation |
US4721537A (en) * | 1985-10-15 | 1988-01-26 | Rockwell International Corporation | Method of producing a fine grain aluminum alloy using three axes deformation |
WO1987003011A1 (en) * | 1985-11-19 | 1987-05-21 | Aluminum Company Of America | Aluminum-lithium alloys and method of making the same |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1993008314A1 (en) * | 1991-10-25 | 1993-04-29 | Allied-Signal Inc. | Strength enhancement of rapidly solidified aluminum-lithium through double aging |
WO1993017138A1 (en) * | 1992-02-20 | 1993-09-02 | Allied-Signal Inc. | Rapidly solidified aluminum lithium alloys having zirconium for aircraft landing wheel applications |
WO1996018752A1 (en) * | 1994-12-10 | 1996-06-20 | British Aerospace Public Limited Company | Heat treatment of aluminium-lithium alloys |
AU690784B2 (en) * | 1994-12-10 | 1998-04-30 | Bae Systems Plc | Heat treatment of aluminium-lithium alloys |
US5879481A (en) * | 1994-12-10 | 1999-03-09 | British Aerospace Public Limited Company | Heat treatment of aluminium-lithium alloys |
CN1062315C (en) * | 1994-12-10 | 2001-02-21 | Bae系统公共有限公司 | Heat treatment of aluminium-lithium alloys |
Also Published As
Publication number | Publication date |
---|---|
CA2079327A1 (en) | 1991-11-03 |
EP0528811A1 (en) | 1993-03-03 |
AU7582291A (en) | 1991-11-27 |
JPH05506271A (en) | 1993-09-16 |
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