WO1991008319A1 - Improvements in or relating to aluminium alloys - Google Patents

Improvements in or relating to aluminium alloys Download PDF

Info

Publication number
WO1991008319A1
WO1991008319A1 PCT/GB1990/001851 GB9001851W WO9108319A1 WO 1991008319 A1 WO1991008319 A1 WO 1991008319A1 GB 9001851 W GB9001851 W GB 9001851W WO 9108319 A1 WO9108319 A1 WO 9108319A1
Authority
WO
WIPO (PCT)
Prior art keywords
billet
annealing
grain
sheet
intermediate shape
Prior art date
Application number
PCT/GB1990/001851
Other languages
French (fr)
Inventor
Kevin Michael Gatenby
Ian Graham Palmer
Roger Grimes
Original Assignee
Alcan International Limited
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 Alcan International Limited filed Critical Alcan International Limited
Priority to EP91900307A priority Critical patent/EP0504218B1/en
Priority to DE69029146T priority patent/DE69029146T2/en
Publication of WO1991008319A1 publication Critical patent/WO1991008319A1/en
Priority to US08/169,548 priority patent/US5374321A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C21/00Alloys based on aluminium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22FCHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
    • C22F1/00Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
    • C22F1/04Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22FCHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
    • C22F1/00Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
    • C22F1/04Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon
    • C22F1/057Changing 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

  • This invention relates to aluminium alloys containing lithium which are particularly suitable for aerospace construction and have been found to have improved cold rolling characteristics.
  • Such alloys are attractive in providing significant weight reduction, for example of up to 205?, over other aluminium alloys, and it is known that they can present high strength and stiffness and have good corrosion resistance properties. However, they have, in the past, in comparison with other aircraft alloys been liable to suffer from a reduction in fracture toughness and can be difficult to cold roll.
  • EP-B-0124286 is concerned with an alloy closely similar to the 8090 alloy, except that the copper content thereof has been increased above that described in EP-B-0088511 to at least 1.655 by weight.
  • This alloy is now recognised commercially as "8091".
  • the thermal history of the ingot is recognised as having an important bearing upon the isotropy of the final cold rolled sheet or strip, and also upon the ease with which subsequent cold rolling can be performed.
  • the cast alloy should be homogenised, hot rolled, cold rolled, solution treated, cold water quenched, and then cold worked, e.g. by stretching.
  • a sample of sheet is subjected to a cyclic tensile stress to cause a fatigue crack to grow.
  • the fatigue crack propagates approximately perpendicular to the axis of the tensile load and continues to grow in this
  • EP-A-0210112 there is disclosed a product with an Al base containing (in weight) from 1 to 3.55? Li, up to 4? Cu, up to 5? Mg, up to 35? Zn and additions of Mn, Cr and/or r.r- Zr characterised in that it contains up to 0.10? Zr, up to
  • Zn and additions of Mn, Cr and/or Zr comprising the steps of casting, possibly homogenising, hot rolling and possibly cold rolling with intermediate annealing if necessary, solution heat treating, water quenching, and an under ageing treatment step, characterised in that the percentages of Zr, Mn and Cr are given by the following limits:
  • EP-A-0157711 there is disclosed a process for producing products of Al-base alloys essentially containing Li, Mg and Cu as principal alloy elements comprising manufacture, a homogenization operation, a hot rolling operation, optionally a cold rolling operation with intermediate annealing operations if required, a solution treatment, a quenching operation, an optional controlled cold deformation operation and tempering operation characterised in that the hot rolling operation is carried out in the range of temperatures of between 100° and 420°C.
  • the purpose of the disclosed method is to obtain a product having a high level of ductility and isotropy.
  • one of the described optional steps is an annealing operation which can be carried out in a temperature range of between 200 and 550°C and can last for from a few minutes to several hours.
  • annealing in a furnace at 350°C for ⁇ hours is mentioned. Again there is no recognition in this publication of the significant effect that annealing at this point in the production route can have on the final product's damage tolerance.
  • Al-Li alloy blanks or sheet subject to conventional annealing treatments, are prone to edge cracking during cold reductions by cold rolling, or splitting during coiling after cold rolling.
  • these problems are avoided by limiting the cold reduction per pass through the rolling mill to about 15? or less and by carrying out an intermediate anneal after each pass or every second pass through the mill.
  • Substantial savings in production time and production costs could be achieved by increasing the reduction per pass and/or the number of passes between each intermediate anneal.
  • the lower temperature limit is set by (a) the appearance in the annealed structure of a coarse precipitate designated delta prime ( £') which is found to be detrimental to the subsequent cold rolling behaviour, and (b) the requirement to achieve sufficient softening of the worked alloy for subsequent rolling.
  • delta prime £'
  • Raising the annealing temperature above about 350°C has been found to cause rapid formation of a coarse, brittle, intermetallic phase.
  • This phase which is of somewhat variable composition, but which is denoted as "C phase” (see K. Gatenby's Ph.D. Thesis of 1988 from The University of Birmingham, England), has a very detrimental effect on cold rolling behaviour, since it causes cracking of the sheet or strip.
  • the C phase particles are fractured during rolling, thereby creating voids in the structure which are retained after annealing.
  • the other grain-controlling elements are selected from hafnium, niobium, scandium, cerium, chromium, titanium and vanadium, and wherein at least one of (i) manganese, (ii) zirconium and (iii) one of the said other grain controlling elements is present,
  • step (c) annealing the said intermediate shape at a temperature sufficiently high for the intermediate shape to be softened sufficiently to be subsequently rolled, and high enough for essentially no £' precipitate to be formed, but not so high as to form any significant amount of C phase, and for a time sufficient to precipitate any soluble constituents therein to an extent sufficient to decrease significantly the extent of work hardening needed in step (d) ,
  • step (d) cold rolling the annealed intermediate shape to an extent sufficient to cause an essentially fully recrystallised grain structure to be formed therein during step (e) and to produce a sheet or strip of the desired thickness
  • the billet is provided in the form of a casting.
  • two additional steps are needed:-
  • the billet can, however, be provided by any other known technique, for example, spray deposition or powder technology. In these cases, the above two optional steps may not be needed.
  • the recrystallised sheet or strip can optionally be recrystallised again, by repeating the above steps starting again from step (c), or possibly from step (d). It has been found that a second recrystallisation is significantly easier to achieve than the first recrystallisation in that the amount of cold rolling required to achieve complete recrystallisation is significantly less (10-20?) as compared with 30-40? for the first recrystallisation. The easier second recrystallisation is probably a result of loss of coherency of the Al-,Zr dispersoid particles which occur as a result of the first recrystallisation, with the incoherent Al Zr being less effective in preventing subsequent recrystallisation.
  • the aluminium-lithium alloys used in the present invention contain magnesium and copper and at least one grain- controlling element in an amount sufficient to produce a dispersion of particles capable of preventing grain coarsening, whilst allowing recrystallisation to occur during the later processing steps.
  • Zirconium is the preferred grain-controlling element, but other elements including hafnium, niobium, scandium, cerium, chromium, manganese, titanium or vanadium or mixtures thereof, may be used with or without zirconium. Generally, zirconium is used in an amount of up to 0.15? by weight, preferably 0.05 to 0.10?
  • zirconium or other grain-refining elements will depend upon the precise casting conditions used, the size of the cast ingot, the particular ingot cooling system used, and upon the subsequent annealing processes. Usually a balance is struck between having a Zr content low enough to allow full recrystallisation to occur during the heat treatment step, which is essential, and a reasonably high Zr content in order to have a useful grain-controlling effect.
  • the preferred range is 0.7 to 1.4?, desirably 0.8 to 1.2? by weight, whilst for copper the preferred range is 1.0 to 1.4?, desirably 1.10 to 1.30? by weight.
  • manganese is beneficial as it both functions as a grain-controlling element and encourages recrystallisation and can be added up to 0.9?, in practice there is a reluctance to add this element because it creates problems in recycling the scrap metal. Since it does provide some grain-controlling effect, however, when present the preferred range for manganese is up to 0.5? by weight.
  • the remaining content of the alloy is preferably as for AA 8090, but here zinc may be present in amounts up to 0.5? as an intentional addition or as a tramp element arising, for example, as a result of recycling Al-Li alloy products which had been clad with an Al-Zn alloy.
  • the alloy is cast, preferably by the direct chill method, and then heated at a controlled rate to a temperature sufficient to relieve internal stresses caused by the cooling from melt of the molten alloy.
  • a temperature sufficient to relieve internal stresses caused by the cooling from melt of the molten alloy.
  • this is generally between 300 and 500°C, preferably between 300 and 400°C. During this heating, some precipitation of at least some of the constituents held in super-saturated solid solution may occur.
  • the stress- relieved billet is heated at a controlled rate such that the low melting point phases are substantially all dissolved without melting, and the billet homogenised by holding it at a temperature and for a time sufficient to dissolve substantially all of the soluble phases.
  • the billet may then be cooled to room temperature and scalped.
  • the homogenised billet is then reheated generally to between 535 and 545°C and hot rolled, optionally with re-heating at intermediate stages, and optionally with hot widening, i.e. cross-rolling at elevated temperature, to produce an intermediate shape suitable for annealing.
  • the hot rolled metal may be heated to about 450°C in order to allow alteration of the distribution of the second phase particles to occur.
  • the hot rolled material is then annealed in order to precipitate any soluble constituents therein in order to reduce the extent of work hardening during cold rolling.
  • this is generally performed at between about 270°C and 350°C, preferably between about 270° and 325°C, and more preferably about 300°C, depending on the precise composition of the alloy used.
  • the annealing temperature should be sufficiently high for the intermediate shape to be softened sufficiently to be subsequently rolled, and high enough for essentially no precipitate to be formed, but not so high as to form any significant amount of C phase.
  • the annealed material is then cold rolled to its final thickness, optionally with inter-annealing usually between 270 and 350°C, such that sufficient cold work is imparted to the sheet or strip to cause a fine re-crystallised grain structure to be formed during solution treatment.
  • the cold-rolled sheet or strip is then rapidly heated to a suitable heat-treatment temperature, preferably in a salt bath, and rapidly cooled, preferably by water quench, in order to produce a solution-treated, fully recrystallised grain structure therein.
  • a suitable heat-treatment temperature preferably in a salt bath
  • water quench preferably by water quench
  • this heat treatment can be done in two steps, the first step at a lower temperature of from about 450°C to below about 530°C in order to bring about recrystallisation and then a second step at about 530°C followed by water quench to solution treat the sheet or strip.
  • the heating step can be carried out using a continuous heat treatment furnace, an air-recirculating furnace or by induction heating, but a salt bath is preferred.
  • recrystallisation can be performed again starting again from step 4 or from step 5 as previously discussed.
  • the quenched sheet or strip is then if desired stretched and/or planished and then under aged, for example at about 150°C for 24 hours, to produce the finished product. Natural ageing may be possible for certain alloys depending on the particular combination of toughness and strength that is desired.
  • a manganese-containing alloy was made according to the present invention.
  • composition A of Table 1 An ingot having composition A of Table 1 was cast by direct chill casting and then stress relieved followed by homogenisation at 54 ⁇ °C.
  • the ingot was hot rolled to a blank 4 mm thick and then annealed for 8 hours at 300°C.
  • the blank was then cold rolled to 3.0 mm thick and annealed again at 300°C for 8 hours.
  • the blank was then cold rolled to 1.6 mm thick and solution treated in a salt bath for 10 minutes at 530°C and water quenched. After planishing and stretching by 2? the strip was aged for 24 hours at 150°C.
  • Example 2 An ingot having the composition B in Table 1 was cast and then hot and cold rolled as described in Example 1 above.
  • the grain size and mechanical properties of the finished sheet are given in Table 2.
  • Example 2 An ingot having the composition C in Table 1 was processed as in Example 1. The recrystallised grain size and the mechanical properties of the finished sheet are given in Table 2.
  • Example 1 An ingot having the composition D in Table 1 was processed as in Example 1 except that after cold rolling to a thickness of 1.4 mm, some of the cold rolled sheet was recrystallised in a salt bath for 30 minutes at 530 C and then cold water quenched to give a fine equiaxed recrystallised grain structure (D1), and some was recrystallised in a pre-heated air recirculating furnace for 30 minutes at 530°C and then cold water quenched to give a fine lamellar recrystallised grain structure (D2). Both materials were stretched 2? and then aged for different times at 150°C to give similar proof strength levels.
  • the recrystallised grain size, tensile and fracture toughness properties of the sheets are given in Table 3.
  • Samples of the salt bath recrystallised material from Example 4 were then cold rolled to a range of reductions including 5? and 12?.
  • the samples were then annealed in a salt bath for 30 minutes at 530°C. On examination of the grain structure, it was found that the sample rolled 5? exhibited excessive secondary grain growth whereas the samples rolled 12? or more showed fine fully recrystallised grain structures.
  • the Example shows that the second recrystallisation can be induced after lower strains than the first recrystallisation.
  • a cast billet of 8090 standard material was stress relieved, homogenised and reheated to 540°C before hot rolling to 6 mm thick. Samples of the sheet were then annealed for 16 hours at a temperature between 275 and 475°C and then cold rolled to 40? reduction in thickness. For comparison, a sample of the as hot rolled material was also cold rolled to 40? reduction in thickness.
  • the thickness used was 0.100" (2.54 mm) .
  • Samples of hot rolled strip of thickness 6.4 mm and composition (wt?) 2.48 Li - 1.22 Cu - 0.83 Mg - 0.069 Zr were annealed at 300°C and 350°C for times of 1, 2, 4, 8, 16 and 32 h, respectively, followed by air cooling. For comparison some samples were cooled using slow furnace cooling for annealing times of 1h and I6h. The tensile properties of the samples were determined and are set out in Table 4.

Landscapes

  • 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)
  • Metal Rolling (AREA)

Abstract

This invention relates to aluminium alloys containing lithium which are particularly suitable for aerospace construction in that they possess improved cold rolling characteristics optionally with improved damage tolerence. A method of producing sheet or strip material is described which comprises the steps of: (a) providing, in a condition suitable for hot rolling, a billet of an alloy of the composition in weight percent: lithium 1.9 to 2.6; magnesium 0.4 to 1.4; copper 1.0 to 2,2; manganese 0 to 0.9; zirconium 0 to 0.25; at least one other grain-controlling element 0 to 0.5; nickel 0 to 0.5; zinc 0 to 0.5; aluminium balance (except for incidental impurities), wherein the other grain-controlling elements are selected from hafnium, niobium, scandium, cerium, chromium, titanium and vanadium, and wherein at least one of (i) manganese, (ii) zirconium and (iii) one of the said other grain controlling elements is present, (b) hot rolling the billet to produce an intermediate shape suitable for annealing, (c) annealing the said intermediate shape at a temperature sufficiently high for the intermediate shape to be softened sufficiently to be subsequently rolled, and high enough for essentially no δ' precipitate to be formed, but not so high as to form any significant amount of C phase, and for a time sufficient to precipitate any soluble constituents therein to an extent sufficient to decrease significantly the extent of work hardening needed in step (d), (d) cold rolling the annealed intermediate shape to an extent sufficient to cause an essentially fully recrystallised grain structure to be formed therein during step (e) and to produce a sheet or strip of the desired thickness, and (e) rapidly heating and rapidly cooling the cold rolled sheet or strip material to produce an essentially fully recrystallised grain structure therein. The preferred temperature range for the annealing step (c) is from 270 °C to 350 °C.

Description

IMPROVEMENTS IN OR RELATING TO ALUMINIUM ALLOYS
This invention relates to aluminium alloys containing lithium which are particularly suitable for aerospace construction and have been found to have improved cold rolling characteristics.
Such alloys are attractive in providing significant weight reduction, for example of up to 205?, over other aluminium alloys, and it is known that they can present high strength and stiffness and have good corrosion resistance properties. However, they have, in the past, in comparison with other aircraft alloys been liable to suffer from a reduction in fracture toughness and can be difficult to cold roll.
Working with small additions of magnesium, copper and zirconium, one successful aluminium-lithium alloy which has been developed commercially is that designated "8090" and described and claimed in EP-B-0088511. This known alloy has the following composition in weight percent:-
lithium 2.0 to 2.8 magnesium 0.4 to 1.0 copper 1.0 to 1.5 zirconium up to 0.2 manganese 0 to 0.5 nickel 0 to 0.5 chromium 0 to 0.5 aluminium balance (except for incidental impurities)
This known alloy when measured against previous Al-Li alloys, such as X2020, demonstrates improved fracture toughness whilst not losing other desirable features such as adequate strength. In EP-B-0088511 , the importance of zirconium in controlling grain size and grain growth on recrystallisation is recognised, and the processing of an alloy ingot through the stages of homogenisation, hot working, cold rolling with inter-stage annealing, solution treatment, water quench and stretching is described.
EP-B-0124286 is concerned with an alloy closely similar to the 8090 alloy, except that the copper content thereof has been increased above that described in EP-B-0088511 to at least 1.655 by weight. This alloy is now recognised commercially as "8091". In this patent, the thermal history of the ingot is recognised as having an important bearing upon the isotropy of the final cold rolled sheet or strip, and also upon the ease with which subsequent cold rolling can be performed. Specifically, it is taught in that patent that the cast alloy should be homogenised, hot rolled, cold rolled, solution treated, cold water quenched, and then cold worked, e.g. by stretching.
It has now been found that by using appropriate processing and heat treatment conditions it is possible to produce a sheet or strip material from Al-Li alloys having improved cold rolling characteristics optionally with improved damage tolerance coupled with adequate strength for aerospace construction.
Since "damage tolerance" does not have a precise definition, a set of typical values for the aluminium alloys of the present invention are:-
Tensile properties:
0.2? Proof strength > 290 MPa
Tensile strength >400 MPa
Elongation to fracture 105- Fracture toughness ( c) measured according to ASTM 561:
For a 1.6 mm thick sheet:
Panel Width 760 mm 500 mm 400 mm
L-T orientation > 105 MPa ϋT >90 Mpa m >85 MPa/m T-L orientation > 95 MPa/fii >8θ Mpa/m >75 MPa/πT
10
Fatigue crack growth:
For a 1.6 mm thick sheet da/dn < 0.7 x 10 -4 mm/cycle
15
(Stress intensity factor range = 10 MPa/πT: stress ratio = 0.1)
With regard to fatigue crack growth, in a test of damage
20 tolerance which is applicable to pressurised fuselage structures, a sample of sheet is subjected to a cyclic tensile stress to cause a fatigue crack to grow. The fatigue crack propagates approximately perpendicular to the axis of the tensile load and continues to grow in this
25 direction until failure occurs. In a sheet of an Al-Li alloy the fatigue crack tends to deviate from the perpendicular direction to grow in a direction closer to parallel to the tensile axis, unless the alloy's composition and the sheet's production history have been
30 suitably controlled.
In EP-A-0210112 there is disclosed a product with an Al base containing (in weight) from 1 to 3.55? Li, up to 4? Cu, up to 5? Mg, up to 35? Zn and additions of Mn, Cr and/or r.r- Zr characterised in that it contains up to 0.10? Zr, up to
0.8? Mn, up to 0.2? Cr with ?Zr/0.03 + ?Mn/0.3 + ?Cr/0.07 ^ 1, and in that its structure is recrystallised with an average grain size that is less than or equal to 200 urn. There is also disclosed a method of obtaining a recrystallised alloy based on Al and containing (in weight) from 1 to 3.5? Li, up to 4? Cu, up to 5? Mg, up to 3? Zn and additions of Mn, Cr and/or Zr comprising the steps of casting, possibly homogenising, hot rolling and possibly cold rolling with intermediate annealing if necessary, solution heat treating, water quenching, and an under ageing treatment step, characterised in that the percentages of Zr, Mn and Cr are given by the following limits:
Zr ,<: 0.10? Mn -£0.8? Cr .S0.20? with ?Zr/0.03 + ?Mn/0.3 + ?Cr/0.07 > 1.
In this published document there is a specific teaching of an intermediate annealing step at 450°C and general guidance to use a temperature of from 200 to 500°C. However, it has now been found that within this described range of temperature there occurs a diversity of metallurgical changes that have a profound effect on the behaviour of the metal during subsequent cold rolling and, equally importantly, during recrystallisation after cold rolling.
Similarly in EP-A-0157711 there is disclosed a process for producing products of Al-base alloys essentially containing Li, Mg and Cu as principal alloy elements comprising manufacture, a homogenization operation, a hot rolling operation, optionally a cold rolling operation with intermediate annealing operations if required, a solution treatment, a quenching operation, an optional controlled cold deformation operation and tempering operation characterised in that the hot rolling operation is carried out in the range of temperatures of between 100° and 420°C. The purpose of the disclosed method is to obtain a product having a high level of ductility and isotropy. In the method one of the described optional steps is an annealing operation which can be carried out in a temperature range of between 200 and 550°C and can last for from a few minutes to several hours. In the Examples annealing in a furnace at 350°C for λ hours is mentioned. Again there is no recognition in this publication of the significant effect that annealing at this point in the production route can have on the final product's damage tolerance.
It has now surprisingly been found that there is a very distinct advantage in carrying out this intermediate annealing step within a relatively narrow temperature range, usually between about 270 and 350°C. Annealing within this temperature range results in a fine, substantially uniform precipitate being formed on cooling to room temperature with only relatively small amounts of solute elements retained in solution in the matrix. Material having this metallurgical structure is found, after cold rolling, to recrystallise easily during the final annealing treatment to yield a product with good damage tolerance. It has further been found that the material is amenable to cold rolling.
Al-Li alloy blanks or sheet, subject to conventional annealing treatments, are prone to edge cracking during cold reductions by cold rolling, or splitting during coiling after cold rolling. In conventional rolling practice on a commercial production mill, these problems are avoided by limiting the cold reduction per pass through the rolling mill to about 15? or less and by carrying out an intermediate anneal after each pass or every second pass through the mill. Substantial savings in production time and production costs could be achieved by increasing the reduction per pass and/or the number of passes between each intermediate anneal. In the course of investigating the improved damage tolerance of aluminum lithium alloys, it has surprisingly been found that there is substantial improvement in the cold rolling behaviour of material annealed under conditions which produce the metallurgical structure described above. Such material is capable of being cold rolled on a commercial mill to reductions of up to 25? or more per pass, and two or more passes may be given between annealing treatments without detrimental edge cracking or splitting occurring.
The lower temperature limit is set by (a) the appearance in the annealed structure of a coarse precipitate designated delta prime ( £') which is found to be detrimental to the subsequent cold rolling behaviour, and (b) the requirement to achieve sufficient softening of the worked alloy for subsequent rolling. A description of & 'can be found in . Gatenby's Ph.D. Thesis of 1988 from The University of Birmingham, England. For the preferred aluminium-lithium alloys used in the present invention ' has been found not to appear at temperatures above about 270°C.
Raising the annealing temperature above about 350°C has been found to cause rapid formation of a coarse, brittle, intermetallic phase. This phase, which is of somewhat variable composition, but which is denoted as "C phase" (see K. Gatenby's Ph.D. Thesis of 1988 from The University of Birmingham, England), has a very detrimental effect on cold rolling behaviour, since it causes cracking of the sheet or strip. The C phase particles are fractured during rolling, thereby creating voids in the structure which are retained after annealing.
Although the C phase is absent from samples annealed at 450°c, it is found that annealing at this high temperature increases the amount of solute element held in solution in the matrix on cooling to room temperature. This results in two detrimental effects:- (a) The work hardening rate during cold rolling is much higher after annealing at 450°C than it is after annealing at 350°C. For example an 8090 alloy given an intermediate anneal at 350°C and cold rolled to 65? reduction had a hardness of about 100 VPN, whereas an identical material given the same rolling reduction after an anneal at 450°C had a hardness of 130 VPN. This higher hardness is reflected in greater roll loads, and hence increased difficulty in rolling, and in a greater tendency to cracking, and
(b) Recrystallisation after cold rolling is more difficult to achieve when the intermediate anneal has been carried out at 450°C. An 8090- alloy annealed at 350°C and cold rolled to 37? reduction in thickness was completely recrystallised after a standard anneal of 10 to 20 minutes at 530 C in a salt bath. Similar material annealed at 450°C and rolled to the same reduction showed only slight recrystallisation after annealing at 530°C and complete recrystallisation was not observed until a 73? cold reduction was employed followed by the standard salt bath anneal.
In accordance with the present invention there is provided a method of producing sheet or strip material of improved cold rolling characteristics optionally with improved damage tolerance which comprises the steps of:-
(a) providing, in a condition suitable for hot rolling, a cast billet of an alloy of the composition in weight percent:-
lithium 1.9 to 2.6 magnesium 0.4 to 1.4 copper 1.0 to 2.2 manganese 0 to 0.9 zirconium 0 to 0.25 at least one other grain-controlling element 0 to 0.5 nickel 0 to 0.5 zinc 0 to 0.5 aluminium balance (except for incidental impurities)
wherein the other grain-controlling elements are selected from hafnium, niobium, scandium, cerium, chromium, titanium and vanadium, and wherein at least one of (i) manganese, (ii) zirconium and (iii) one of the said other grain controlling elements is present,
(b) hot rolling the billet to produce an intermediate shape suitable for annealing,
(c) annealing the said intermediate shape at a temperature sufficiently high for the intermediate shape to be softened sufficiently to be subsequently rolled, and high enough for essentially no £' precipitate to be formed, but not so high as to form any significant amount of C phase, and for a time sufficient to precipitate any soluble constituents therein to an extent sufficient to decrease significantly the extent of work hardening needed in step (d) ,
(d) cold rolling the annealed intermediate shape to an extent sufficient to cause an essentially fully recrystallised grain structure to be formed therein during step (e) and to produce a sheet or strip of the desired thickness, and
(e) rapidly heating and rapidly cooling the cold rolled sheet or strip material to produce an essentially fully recrystallised grain structure therein.
Generally the billet is provided in the form of a casting. In order to bring the billet in a condition for hot rolling the following two additional steps are needed:-
(1) heating the cast billet to a temperature and for a time sufficient to relieve internal stresses in the billet caused by its cooling and solidi ication from the molten state, (2) heating the stress-relieved billet to a temperature and at a rate and for a time sufficient to cause essentially all of the low melting point phases in the billet to be dissolved without melting and a homogenised billet to be produced.
The billet can, however, be provided by any other known technique, for example, spray deposition or powder technology. In these cases, the above two optional steps may not be needed.
With some of the alloys used in the present invention, it has been found that they age at room temperature to an extent sufficient to produce a sheet or strip of improved damage tolerance. With other alloys, however, a distinct ageing step is necessary. In either case, ageing can be preceded by a stretching or planishing step if required.
Furthermore, prior to ageing the recrystallised sheet or strip can optionally be recrystallised again, by repeating the above steps starting again from step (c), or possibly from step (d). It has been found that a second recrystallisation is significantly easier to achieve than the first recrystallisation in that the amount of cold rolling required to achieve complete recrystallisation is significantly less (10-20?) as compared with 30-40? for the first recrystallisation. The easier second recrystallisation is probably a result of loss of coherency of the Al-,Zr dispersoid particles which occur as a result of the first recrystallisation, with the incoherent Al Zr being less effective in preventing subsequent recrystallisation.
The aluminium-lithium alloys used in the present invention contain magnesium and copper and at least one grain- controlling element in an amount sufficient to produce a dispersion of particles capable of preventing grain coarsening, whilst allowing recrystallisation to occur during the later processing steps. Zirconium is the preferred grain-controlling element, but other elements including hafnium, niobium, scandium, cerium, chromium, manganese, titanium or vanadium or mixtures thereof, may be used with or without zirconium. Generally, zirconium is used in an amount of up to 0.15? by weight, preferably 0.05 to 0.10? and more preferably 0.05 to 0.07?, although the precise amount of zirconium or other grain-refining elements will depend upon the precise casting conditions used, the size of the cast ingot, the particular ingot cooling system used, and upon the subsequent annealing processes. Usually a balance is struck between having a Zr content low enough to allow full recrystallisation to occur during the heat treatment step, which is essential, and a reasonably high Zr content in order to have a useful grain-controlling effect.
Because it has been found that with a lithium content greater than 2.60? by weight the resulting sheet or strip material is difficult to cold roll, preferably values of lithium no higher than 2.5 and down to 2.20? by weight are used, more preferably from 2.25 to 2.45? by weight.
For magnesium, the preferred range is 0.7 to 1.4?, desirably 0.8 to 1.2? by weight, whilst for copper the preferred range is 1.0 to 1.4?, desirably 1.10 to 1.30? by weight.
Although the presence of manganese is beneficial as it both functions as a grain-controlling element and encourages recrystallisation and can be added up to 0.9?, in practice there is a reluctance to add this element because it creates problems in recycling the scrap metal. Since it does provide some grain-controlling effect, however, when present the preferred range for manganese is up to 0.5? by weight. The remaining content of the alloy is preferably as for AA 8090, but here zinc may be present in amounts up to 0.5? as an intentional addition or as a tramp element arising, for example, as a result of recycling Al-Li alloy products which had been clad with an Al-Zn alloy.
The processing steps for the production of sheet or strip material in accordance with the present invention using an initial casting method are as follows:-
1. The alloy is cast, preferably by the direct chill method, and then heated at a controlled rate to a temperature sufficient to relieve internal stresses caused by the cooling from melt of the molten alloy. For the preferred alloys described above, this is generally between 300 and 500°C, preferably between 300 and 400°C. During this heating, some precipitation of at least some of the constituents held in super-saturated solid solution may occur.
2. Either with intermediate cooling or following directly on from the heating step 1 , the stress- relieved billet is heated at a controlled rate such that the low melting point phases are substantially all dissolved without melting, and the billet homogenised by holding it at a temperature and for a time sufficient to dissolve substantially all of the soluble phases. The billet may then be cooled to room temperature and scalped.
3. The homogenised billet is then reheated generally to between 535 and 545°C and hot rolled, optionally with re-heating at intermediate stages, and optionally with hot widening, i.e. cross-rolling at elevated temperature, to produce an intermediate shape suitable for annealing. If desired, the hot rolled metal may be heated to about 450°C in order to allow alteration of the distribution of the second phase particles to occur.
4. The hot rolled material is then annealed in order to precipitate any soluble constituents therein in order to reduce the extent of work hardening during cold rolling. For the preferred alloys described above this is generally performed at between about 270°C and 350°C, preferably between about 270° and 325°C, and more preferably about 300°C, depending on the precise composition of the alloy used. As discussed above, the annealing temperature should be sufficiently high for the intermediate shape to be softened sufficiently to be subsequently rolled, and high enough for essentially no precipitate to be formed, but not so high as to form any significant amount of C phase.
5. The annealed material is then cold rolled to its final thickness, optionally with inter-annealing usually between 270 and 350°C, such that sufficient cold work is imparted to the sheet or strip to cause a fine re-crystallised grain structure to be formed during solution treatment.
6. The cold-rolled sheet or strip is then rapidly heated to a suitable heat-treatment temperature, preferably in a salt bath, and rapidly cooled, preferably by water quench, in order to produce a solution-treated, fully recrystallised grain structure therein. It should be noted that this heat treatment can be done in two steps, the first step at a lower temperature of from about 450°C to below about 530°C in order to bring about recrystallisation and then a second step at about 530°C followed by water quench to solution treat the sheet or strip. The heating step can be carried out using a continuous heat treatment furnace, an air-recirculating furnace or by induction heating, but a salt bath is preferred.
7. Optionally recrystallisation can be performed again starting again from step 4 or from step 5 as previously discussed.
8. The quenched sheet or strip is then if desired stretched and/or planished and then under aged, for example at about 150°C for 24 hours, to produce the finished product. Natural ageing may be possible for certain alloys depending on the particular combination of toughness and strength that is desired.
Embodiments of the present invention will now be described by way of example with reference to the following Examples and the accompanying drawing.
ExamDle 1
A manganese-containing alloy was made according to the present invention.
An ingot having composition A of Table 1 was cast by direct chill casting and then stress relieved followed by homogenisation at 54θ°C. The ingot was hot rolled to a blank 4 mm thick and then annealed for 8 hours at 300°C. The blank was then cold rolled to 3.0 mm thick and annealed again at 300°C for 8 hours. The blank was then cold rolled to 1.6 mm thick and solution treated in a salt bath for 10 minutes at 530°C and water quenched. After planishing and stretching by 2? the strip was aged for 24 hours at 150°C.
The recrystallised grain size, tensile and fracture toughness properties of the sheet are given in Table 2. This alloy had good mechanical properties but, for the reasons mentioned earlier, it is sometimes preferable to avoid Mn additions. Fatigue properties were found to be superior to a clad 2024 alloy tested under similar conditions.
Example 2
An ingot having the composition B in Table 1 was cast and then hot and cold rolled as described in Example 1 above. The grain size and mechanical properties of the finished sheet are given in Table 2.
When fatigue tests were carried out, it was found that the fatigue cracks initially grew in a direction perpendicular to the tensile stress axis but subsequently showed significant deviation, on a macroscopic scale, towards this axis. Whilst this fatigue crack behaviour is unacceptable in certain aircraft structures, such as skinning sheet of large passenger aircraft, it would not be unacceptable in other areas requiring high damage tolerance, e.g. fuselage frames fabricated from sheet material.
Example 3
An ingot having the composition C in Table 1 was processed as in Example 1. The recrystallised grain size and the mechanical properties of the finished sheet are given in Table 2.
When fatigue tests were carried out on this alloy, it was found that the cracks grew perpendicular to the stress axis without macroscopic crack deviation. TABLE 1
INGOT Li Cu Mg Zr Mn
0.29
Figure imgf000017_0001
TABLE 2
B
Figure imgf000017_0002
Notes: 1 - for a 760 mm wide panel
2 - for a 500 mm wide panel
3 - measured according to ASTM E112
Example 4
An ingot having the composition D in Table 1 was processed as in Example 1 except that after cold rolling to a thickness of 1.4 mm, some of the cold rolled sheet was recrystallised in a salt bath for 30 minutes at 530 C and then cold water quenched to give a fine equiaxed recrystallised grain structure (D1), and some was recrystallised in a pre-heated air recirculating furnace for 30 minutes at 530°C and then cold water quenched to give a fine lamellar recrystallised grain structure (D2). Both materials were stretched 2? and then aged for different times at 150°C to give similar proof strength levels. The recrystallised grain size, tensile and fracture toughness properties of the sheets are given in Table 3.
It can be seen that both materials show high levels of fracture toughness. (The toughness values obtained for these 1.4 mm thick materials are slightly lower than those shown in Table 2 for 1.6 mm thick material, as a result of both the decrease in sheet thickness, and the use of a narrower test panel width.)
TABLE 3
Example Age PS TS El. Kc *(L-T) Grain Size
(hr/°C) (MPa) (MPa) (?) (MPa/m) (pm)
D1 16/150 L 325 434 12.5 134 18
D2 64/150 L 329 419 9.0 125 23 x 40
* 400 mm wide panel
Example 5
Samples of the salt bath recrystallised material from Example 4 were then cold rolled to a range of reductions including 5? and 12?. The samples were then annealed in a salt bath for 30 minutes at 530°C. On examination of the grain structure, it was found that the sample rolled 5? exhibited excessive secondary grain growth whereas the samples rolled 12? or more showed fine fully recrystallised grain structures.
It has been found that hot rolled blank given an intermediate anneal at about 300°C will not fully recrystallise during annealing at 530°C until it has received about 30? cold reduction.
The Example shows that the second recrystallisation can be induced after lower strains than the first recrystallisation.
Although described with reference to the batch treatment of sheets, it will be appreciated that it is possible to carry out the treatments in a continuous heat treatment line. It has been found that a two-step annealing treatment, which could most conveniently be done on a continuous heat treatment line has a surprising effect on the finished sheet as Example 5 shows.
Example 6
A cast billet of 8090 standard material was stress relieved, homogenised and reheated to 540°C before hot rolling to 6 mm thick. Samples of the sheet were then annealed for 16 hours at a temperature between 275 and 475°C and then cold rolled to 40? reduction in thickness. For comparison, a sample of the as hot rolled material was also cold rolled to 40? reduction in thickness.
Specimens prepared for the Kahn Tear Test (see Alcoa Technical Paper 18 published in 1965 entitled "Fracture Characteristics of Aluminium Alloys" by J. Kaufman and M. Holt) were taken and tested using known procedures to establish the energy required to initiate a crack and the energy required to propagate a crack. A pronounced increase in the crack propagation energy was observed in those samples annealed between 275° and 350°C as shown in Figure 1. Above 350° the crack propagation energy decreases eventually falling to a level only slightly above that of the sample cold rolled without the intermediate anneal. These results demonstrate that the optimum temperature for annealing lies between 275 and 350°C since metal annealed in this temperature range is less likely to crack during subsequent cold deformation.
For the Kahn Tear Test the thickness used was 0.100" (2.54 mm) .
Example 7
Samples of hot rolled strip of thickness 6.4 mm and composition (wt?) 2.48 Li - 1.22 Cu - 0.83 Mg - 0.069 Zr were annealed at 300°C and 350°C for times of 1, 2, 4, 8, 16 and 32 h, respectively, followed by air cooling. For comparison some samples were cooled using slow furnace cooling for annealing times of 1h and I6h. The tensile properties of the samples were determined and are set out in Table 4.
It can be seen that for both annealing temperatures the proof strength and ultimate strength levels decrease and the ductility increases with increased annealing time. Longer annealing times (16 h) therefore result in material which is significantly softer and more ductile than after shorter annealing times (1-2 h) , even if the shorter times are followed by slow furnace cooling. The optimum annealing treatment, which produced low strength levels and the highest ductility, was found to be 16 h, at 300°C.
It is noteworthy that these results demonstrate that the lowest strength and highest ductility occurs at a much longer treatment time than those recited in Examples 2 and 3 of EP-A-0157711. Furthermore, the strength and ductility levels are not significantly influenced by the rate of cooling from the annealing temperature.
Whilst it is known that extended annealing times, or higher temperatures, may increase ductility and reduce strength of many alloys, it is surprising that this is observed in this temperature range in the Al-Li alloys of this invention which, on heating, are prone to form intermetallic phases which can adversely affect strength and/or ductility.
Figure imgf000021_0001

Claims

CLAIMS :
1. A method of producing sheet or strip material of improved cold rolling characteristics optionally with improved damage tolerance which comprises the steps of:-
(a) providing, in a condition suitable for hot rolling, a billet of an alloy of the composition in weight percent:-
lithium 1.9 to 2.6 magnesium 0.4 to 1.4 copper 1.0 to 2.2 manganese 0 to 0.9 zirconium 0 to 0.25 at least one other grain-controlling element 0 to 0.5 nickel 0 to 0.5 zinc 0 to 0.5 aluminium balance (except for incidental impurities)
wherein the other grain-controlling elements are selected from hafnium, niobium, scandium, cerium, chromium, titanium and vanadium, and wherein at least one of (i) manganese, (ii) zirconium and (iii) one of the said other grain controlling elements is present,
(b) hot rolling the billet to produce an intermediate shape suitable for annealing,
(c) annealing the said intermediate shape at a temperature sufficiently high for the intermediate shape to be softened sufficiently to be subsequently rolled, and high enough for essentially no £ ' precipitate to be formed, but not so high as to form any significant amount of C phase, and for a time sufficient to precipitate any soluble constituents therein to an extent sufficient to decrease significantly the extent of work hardening needed in step (d) , (d) cold rolling the annealed intermediate shape to an extent sufficient to cause an essentially fully recrystallised grain structure to be formed therein during step (e) and to produce a sheet or strip of the desired thickness, and
(e) rapidly heating and rapidly cooling the cold rolled sheet or strip material to produce an essentially fully recrystallised grain structure therein.
2. A method as claimed in claim 1 wherein the billet is cast and is provided in a condition for hot rolling by the steps of:-
(1) heating the cast billet to a temperature and for a time sufficient to relieve internal stresses in the billet caused by its cooling and solidification from the molten state,
(2) heating the stress-relieved billet to a temperature and at a rate and for a time sufficient to cause essentially all of the low melting point phases in the billet to be dissolved without melting and a homogenised billet to be produced.
3. A method as claimed in claim 2 including the step of cooling the stress-relieved billet between steps (1) and (2).
4. A method as claimed in any one of the preceding claims wherein the alloy contains lithium in an amount of from 2.25 to 2.45 percent by weight.
5. A method as claimed in any one of the preceding claims wherein the alloy contains copper in an amount of from 1.10 to 1.30 percent by weight.
6. A method as claimed in any one of the preceding claims wherein the grain-controlling element is zirconium and is present in an amount of from 0.05 to 0.10 percent by weight.
7. A method as claimed in claim 6 wherein the zirconium is present in an amount of from 0.05 to 0.07 percent by weight.
8. A method as claimed in any one of the preceding claims wherein the alloy contains magnesium in an amount of from 0.8 to 1.2 percent by weight.
9. A method as claimed in any one of the preceding claims wherein the alloy contains manganese in an amount of up to 0.5 percent by weight.
10. A method as claimed in any one of the preceding claims wherein the annealing step (c) is carried out at a temperature of from 270°C to 350°C.
11. A method as claimed in claim 10 wherein the annealing step (c) is carried out at a temperature of from 270° to
325°C
12. A method as claimed in any one of the preceding claims including the steps of re-heating and optionally hot widening the homogenised billet during or subsequent to the hot rolling of the billet in step (b) .
13. A method as claimed in any one of the preceding claims including at least one inter-annealing step during the cold rolling of the annealed intermediate shape in step (d).
14. A method as claimed in any one of the preceding claims wherein the heating of the cold rolled sheet or strip material of step (e) is performed in a salt bath.
15. A method as claimed in any one of the preceding claims wherein the cooling of the heated cold rolled sheet or strip material of step (e) is performed using a water quench.
16. A method as claimed in any one of the preceding claims wherein the recrystallised sheet or strip material is recrystallised again by performing again after step (e) either step (c) or step (d) and its following steps.
17. A method as claimed in any one of the preceding claims wherein after step (e) the sheet or strip material is stretched and/or planished and then under aged.
PCT/GB1990/001851 1989-11-28 1990-11-28 Improvements in or relating to aluminium alloys WO1991008319A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
EP91900307A EP0504218B1 (en) 1989-11-28 1990-11-28 Improvements in or relating to aluminium alloys
DE69029146T DE69029146T2 (en) 1989-11-28 1990-11-28 IMPROVEMENTS IN ALUMINUM ALLOYS
US08/169,548 US5374321A (en) 1989-11-28 1993-12-20 Cold rolling for aluminum-lithium alloys

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB8926861.9 1989-11-28
GB898926861A GB8926861D0 (en) 1989-11-28 1989-11-28 Improvements in or relating to aluminium alloys

Publications (1)

Publication Number Publication Date
WO1991008319A1 true WO1991008319A1 (en) 1991-06-13

Family

ID=10667038

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/GB1990/001851 WO1991008319A1 (en) 1989-11-28 1990-11-28 Improvements in or relating to aluminium alloys

Country Status (7)

Country Link
US (1) US5374321A (en)
EP (1) EP0504218B1 (en)
JP (1) JP3022922B2 (en)
AU (1) AU7895991A (en)
DE (1) DE69029146T2 (en)
GB (1) GB8926861D0 (en)
WO (1) WO1991008319A1 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998037250A1 (en) * 1997-02-24 1998-08-27 The Secretary Of State For Defence Aluminium-lithium alloys
WO2008069697A3 (en) * 2006-12-08 2008-08-07 Otkrytoe Akcionernoe Obshhestv Method for producing flat products made of aluminium alloys
RU2507299C2 (en) * 2009-06-23 2014-02-20 Линде Аг Annealing of cold-rolled metallic strip
CN108754358A (en) * 2018-05-29 2018-11-06 江苏理工学院 A kind of low temperature resistant Al alloy composite and preparation method thereof

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7628953B2 (en) * 2004-09-06 2009-12-08 Federalnoe Gosudarstvennoe Unitanoe Predpriyatie “Vserossysky Nauchno-Issledovatelsky Institut Aviatsionnykh Materialov” (FGUP VIAM) Aluminum-based alloy and the article made thereof
RU2461642C1 (en) * 2011-05-12 2012-09-20 Федеральное Государственное Унитарное Предприятие "Центральный Научно-Исследовательский Институт Конструкционных Материалов "Прометей" (Фгуп "Цнии Км "Прометей") Method of hot-rolling of semis from aluminium alloys with scandium
JP5973761B2 (en) * 2012-03-27 2016-08-23 オリンパス株式会社 Cable connection structure
CN104451272B (en) * 2014-11-21 2016-11-23 上海交通大学 High-strength light Casting Al-Li Alloy and preparation method thereof
CN110541131B (en) * 2019-08-29 2021-02-19 哈尔滨工业大学 Al-Cu-Li alloy thermomechanical treatment process based on particle-excited nucleation
CN113182353B (en) * 2021-03-12 2022-09-20 北京北冶功能材料有限公司 Preparation method of nickel-based high-temperature alloy cold-rolled foil for aircraft engine
PL440101A1 (en) 2022-01-04 2023-07-10 Kghm Polska Miedź Spółka Akcyjna Method of obtaining high-ductility Ti-Re alloys, Ti-Re alloys obtained by this method and their application
CN114672686B (en) * 2022-03-21 2022-10-28 华中科技大学 Preparation method of additional nano-particle reinforced cast aluminum-lithium alloy
CN115418534B (en) * 2022-09-19 2023-05-09 郑州轻研合金科技有限公司 8090 aluminum lithium alloy fine-grain plate and preparation method thereof
CN115572924B (en) * 2022-09-28 2023-11-21 中国航发北京航空材料研究院 Technological method for reducing damage tolerance anisotropy of 7000 series aircraft plates

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2137656A (en) * 1983-03-31 1984-10-10 Alcan Int Ltd Aluminium alloy heat treatment
EP0157711A1 (en) * 1984-03-15 1985-10-09 Pechiney Rhenalu Process for the manufacture of objects from Al-Li-Mg-Cu alloys with high ductibility and isotropy properties
EP0210112A1 (en) * 1985-06-25 1987-01-28 Cegedur Pechiney Rhenalu Lithium-containing products based on aluminium for use in the recrystallized condition, and process for their manufacture
US4647318A (en) * 1985-10-03 1987-03-03 Foreman Robert W Solution heat treatment for aluminum alloys
FR2610949A1 (en) * 1987-02-18 1988-08-19 Cegedur Process for desensitising Al alloys containing Li to stress corrosion
EP0394155A1 (en) * 1989-04-21 1990-10-24 Pechiney Rhenalu Damage resistant Al-li-cu-mg alloy having good cold-forming properties

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2626009B2 (en) * 1987-02-18 1992-05-29 Cegedur AL ALLOY PRODUCT CONTAINING LI CORROSION RESISTANT UNDER TENSION

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2137656A (en) * 1983-03-31 1984-10-10 Alcan Int Ltd Aluminium alloy heat treatment
EP0157711A1 (en) * 1984-03-15 1985-10-09 Pechiney Rhenalu Process for the manufacture of objects from Al-Li-Mg-Cu alloys with high ductibility and isotropy properties
EP0210112A1 (en) * 1985-06-25 1987-01-28 Cegedur Pechiney Rhenalu Lithium-containing products based on aluminium for use in the recrystallized condition, and process for their manufacture
US4647318A (en) * 1985-10-03 1987-03-03 Foreman Robert W Solution heat treatment for aluminum alloys
FR2610949A1 (en) * 1987-02-18 1988-08-19 Cegedur Process for desensitising Al alloys containing Li to stress corrosion
EP0394155A1 (en) * 1989-04-21 1990-10-24 Pechiney Rhenalu Damage resistant Al-li-cu-mg alloy having good cold-forming properties

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Journal de Physique,Colloque C3, supplément au no.9,Tome 48,septembre 1987,Proceedings of the Fourth International Aluminium-Lithium Conference,Paris,10-12 June 1987,editions de Physique,(Paris,FR),M.Goncalves et al.:"Static recrystallization after hot working of Al-Li alloys"see pages C3-171-C3-177 *

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998037250A1 (en) * 1997-02-24 1998-08-27 The Secretary Of State For Defence Aluminium-lithium alloys
GB2338491A (en) * 1997-02-24 1999-12-22 Secr Defence Aluminium-lithium alloys
GB2338491B (en) * 1997-02-24 2000-11-08 Secr Defence Aluminium-lithium alloys
US6991689B2 (en) 1997-02-24 2006-01-31 Qinetiq Limited Aluminium-lithium alloys
WO2008069697A3 (en) * 2006-12-08 2008-08-07 Otkrytoe Akcionernoe Obshhestv Method for producing flat products made of aluminium alloys
RU2507299C2 (en) * 2009-06-23 2014-02-20 Линде Аг Annealing of cold-rolled metallic strip
CN108754358A (en) * 2018-05-29 2018-11-06 江苏理工学院 A kind of low temperature resistant Al alloy composite and preparation method thereof
CN108754358B (en) * 2018-05-29 2020-03-17 江苏理工学院 Low-temperature-resistant aluminum alloy composite material and preparation method thereof

Also Published As

Publication number Publication date
US5374321A (en) 1994-12-20
JPH05501588A (en) 1993-03-25
DE69029146T2 (en) 1997-04-10
EP0504218B1 (en) 1996-11-13
DE69029146D1 (en) 1996-12-19
AU7895991A (en) 1991-06-26
GB8926861D0 (en) 1990-01-17
EP0504218A1 (en) 1992-09-23
JP3022922B2 (en) 2000-03-21

Similar Documents

Publication Publication Date Title
US5882449A (en) Process for preparing aluminum/lithium/scandium rolled sheet products
US4946517A (en) Unrecrystallized aluminum plate product by ramp annealing
US4927470A (en) Thin gauge aluminum plate product by isothermal treatment and ramp anneal
US4816087A (en) Process for producing duplex mode recrystallized high strength aluminum-lithium alloy products with high fracture toughness and method of making the same
EP0656956B1 (en) Tough aluminum alloy containing copper and magnesium
US4988394A (en) Method of producing unrecrystallized thin gauge aluminum products by heat treating and further working
EP0247181B1 (en) Aluminum-lithium alloys and method of making the same
WO2008003504A2 (en) Aa7000-series aluminium alloy products and a method of manufacturing thereof
JPH111737A (en) Heat treated type 7000 series aluminum alloy with excellent corrosion resistance and high strength, and its production
US5061327A (en) Method of producing unrecrystallized aluminum products by heat treating and further working
CA3109052A1 (en) Method of manufacturing a 2xxx-series aluminium alloy plate product having improved fatigue failure resistance
WO1992003583A1 (en) Improved lithium aluminum alloy system
EP0517884A1 (en) Low aspect ratio lithium-containing aluminum extrusions
US5374321A (en) Cold rolling for aluminum-lithium alloys
US4961792A (en) Aluminum-lithium alloys having improved corrosion resistance containing Mg and Zn
EP0368005A1 (en) A method of producing an unrecrystallized aluminum based thin gauge flat rolled, heat treated product
EP0281076B1 (en) Aluminum lithium flat rolled product
US5135713A (en) Aluminum-lithium alloys having high zinc
CA1338007C (en) Aluminum-lithium alloys
US4812183A (en) Coated sheet stock
US5137686A (en) Aluminum-lithium alloys
US4921548A (en) Aluminum-lithium alloys and method of making same
US5540791A (en) Preformable aluminum-alloy rolled sheet adapted for superplastic forming and method for producing the same
CN113474479B (en) Method for producing sheet or strip from aluminium alloy and sheet, strip or shaped part produced therefrom
JP2000212673A (en) Aluminum alloy sheet for aircraft stringer excellent in stress corrosion cracking resistance and its production

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AT AU BB BG BR CA CH DE DK ES FI GB GR HU JP KP KR LK LU MC MG MW NL NO RO SD SE SU US

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): AT BE BF BJ CF CG CH CM DE DK ES FR GA GB GR IT LU ML MR NL SE SN TD TG

WWE Wipo information: entry into national phase

Ref document number: 1991900307

Country of ref document: EP

REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

WWP Wipo information: published in national office

Ref document number: 1991900307

Country of ref document: EP

NENP Non-entry into the national phase

Ref country code: CA

WWG Wipo information: grant in national office

Ref document number: 1991900307

Country of ref document: EP