EP0968315A1 - Al-Mg-Si ALLOY WITH GOOD EXTRUSION PROPERTIES - Google Patents
Al-Mg-Si ALLOY WITH GOOD EXTRUSION PROPERTIESInfo
- Publication number
- EP0968315A1 EP0968315A1 EP98912599A EP98912599A EP0968315A1 EP 0968315 A1 EP0968315 A1 EP 0968315A1 EP 98912599 A EP98912599 A EP 98912599A EP 98912599 A EP98912599 A EP 98912599A EP 0968315 A1 EP0968315 A1 EP 0968315A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- extrusion
- alloy
- alloys
- max
- ingot
- 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.)
- Granted
Links
Classifications
-
- 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
- C22C21/02—Alloys based on aluminium with silicon as the next major constituent
-
- 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
- C22F1/043—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 silicon as the next major constituent
-
- 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
- C22F1/05—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 of the Al-Si-Mg type, i.e. containing silicon and magnesium in approximately equal proportions
Definitions
- This invention concerns AIMgSi alloys of the 6000 series of the Aluminum Association Register.
- the compositions are low magnesium containing AIMgSi alloys with appropriate silicon and copper additions to meet the strength requirements of AA6063T5 and T6.
- AA6063 accounts for approximately 80% of all aluminium extruded products. At this bottom end of the extrusion market, there is a need for extrusions which meet the T5 or T6 strength requirements but which can be manufactured at the highest possible rates of extrusion.
- AIMgSi Alloys having the composition in wt%: Mg 0.25 - 0.40; Si 0.60 - 0.90; Fe up to 0.35; Mn up to 0.35 preferably 0.10 - 0.25. But these are not general purpose extrusion alloys. By virtue of the high Si content they have high tensile strength generally in excess of 250 MPa and they preferably contain Mn to improve extrusion surface quality.
- This invention concerns general purpose extrusion alloys having the minimum alloying additions required to meet the strength requirements of AA 6063T5 (peak aged tensile strength of at least about 152 MPa) and T6 (peak aged tensile strength of at least about 207 MPa).
- the lower breakthrough pressure associated with the lower Mg content also means that for a given extrusion press, the initial billet temperature can be reduced until the pressure required matches the press capacity. This has the effect of further reducing the temperature of the product as it exits the die which gives further productivity benefits.
- the invention provides an alloy of composition in wt%
- the invention also provides extrusion ingots of the alloy as defined; and extrusions (i.e. extruded sections) made from such ingots.
- extrusions i.e. extruded sections
- Figure 1 is a graph showing Mg and Si concentrations of certain dilute 6000 alloys.
- Figure 2 is a graph of tensile strength against Si content for alloys of different composition.
- Figure 3 is a graph showing T5 and T6 limits for various dilute 6000 alloys.
- Figure 4 is a graph showing elongation at break for alloys of different composition.
- Figure 5 is a bar chart showing relative mean extrusion breakthrough pressure for alloys of different composition.
- Figure 6 is a graph showing extrusion breakthrough load at 450°C for alloys of different composition.
- Figure 7 is a graph showing extrusion breakthrough load at 425°C for alloys of different composition.
- Figures 8 and 9 are graphs of tensile strength against Si content of two different alloys showing the effects of different ageing practices.
- Figure 10 is a graph showing the effect of silicon content on ⁇ - ⁇ transformation.
- Figure 1 1 is a graph showing the effect of silicon content on AIFeSi intermetallic size.
- Figure 12 is a graph showing the effect of silicon content on AIFeSi spheroidisation.
- Figure 13 is a graph showing the effect of Si and Mn levels on ⁇ - ⁇ transformation.
- Figure 14 is a graph showing the effect of Mg and Si content on roughness of extrusions according to the invention at an extrusion temperature of 450°C.
- Figure 15 is a graph showing the effect of alloy composition on tensile strength.
- the boxes marked A and B designate the broad and narrow compositions of alloys according to the invention as defined above. Also shown for comparison is the bottom end of a box for AA6060, a general purpose extrusion alloy; and the left hand side of a box for the high strength alloy described in WO 95/06759. Lines marked T5 and T6 represent the compositions required to produce extrusions capable of passing these tests. The positions of these lines are somewhat variable depending on ingot pretreatment conditions, rate of cooling the extrusions and extrusion ageing conditions.
- the Mg content of the invention alloy is set at 0.20 - 0.34 preferably 0.20 - 0.30%. If the Mg content is too low, it is difficult to achieve the required strength in the aged extrusions. Extrusion pressure increases with Mg content, and becomes unacceptable at high Mg contents.
- the Si content is set at 0.35 - 0.60 preferably 0.40 - 0.59. If the Si content is too low, the alloy strength is adversely affected, while if the Si content is too high, extrudability may be reduced. Formability has also been reported to be impaired at high Si levels, but it has been found that this effect is not important within the composition range of the invention.
- a function of the Si is to strengthen the alloy without adversely affecting extrudability, high temperature flow stress or anodising and corrosion characteristics.
- Fe in the alloy is normally unavoidable.
- An upper concentration limit is set at 0.35, preferably 0.25%. It is likely to be preferred to use alloys containing at least 0.15% Fe, to prevent bright finish on anodising and because these alloys are less expensive than alloys containing lower Fe concentrations especially when made from remelted scrap.
- Fe is present in the form of large plate- like ⁇ -AIFeSi particles.
- the extrusion ingot is homogenised to convert ⁇ -AIFeSi to substantially (at least 80% and preferably more than 90%) the ⁇ -AIFeSi form.
- Mn has a number of different effects. Although it has previously been included in extrusion alloys to improve toughness, it is generally not useful for this purpose for alloys of the present invention. At very high levels, Mn gives rise to problems with quench sensitivity due to increased levels of dispersoid formation. To avoid this, Mn levels are preferably kept below 0.15% particularly below 0.10%.
- Mn has a hitherto unpublished technical effect.
- silicon levels of about 0.50 wt% or greater lead to increased stability of the ⁇ -AIFeSi phase at homogenisation temperatures. This retards the transformation of the AIFeSi intermetallic from ⁇ to ⁇ during homogenisation. As a result, the break up of the intermetallics is retarded such that mean size of the intermetallic phases is increased and a degree of spheroidisation is reduced. This has detrimental effects on the extrudability of the material and causes poor surface finish.
- the effects of the silicon level on ⁇ stability can be avoided by adding an appropriate level of manganese to the alloy which stabilises the ⁇ form of the AI(Fe,Mn)Si intermetallic. Thus a preferred minimum manganese content can be expressed:-
- Wt% manganese at least 0.3 x wt% silicon - 0.12 Inclusion of manganese in these concentrations helps to: promote a ⁇ to ⁇ AIFeSi transformation during homogenisation such that at least an 80% and preferably at least 90% transformation is achieved under normal homogenising conditions; reduce the AIFeSi particle size (which is however also dependent on the diameter of the billet being homogenised); and increase the degree of AIFeSi spheroidisation, preferably to at least 0.5 or 0.51 (where 0 equals a rod and 1 equals a sphere).
- Cu has the advantage of improving tensile strength without a comparable increase in extrusion breakthrough pressure; and a disadvantage of giving rise to corrosion problems.
- Cu may be included in alloys of this invention at concentrations up to 0.25% preferably up to 0.20%, and particularly up to 0.10%.
- the strength of extrusion alloys is sometimes expressed in terms of their Mg 2 Si content, which for excess Si alloys such as these may be calculated as Mg x1.57.
- the Mg 2 Si content of alloys according to this invention is preferably 0.314 - 0.55 wt%, particularly 0.38 - 0.53 t%.
- Si is present in an excess over that required to combine with all Mg as Mg 2 Si, and with all Fe and Mn as AI(Fe,Mn)Si. (The terms AIFeSi and AI(Fe,Mn)Si are conventionally used to denote intermetallics containing these elements but not necessarily in these proportions).
- the excess Si is preferably 0.08 - 0.48 wt% particularly 0.12 - 0.40 wt%. Where this excess is too small, it will be difficult to achieve the required tensile strength properties. Where this excess is too large, alloy formability and extrusion surface quality may be adversely affected.
- An extrusion ingot of the alloy of the invention may be made by any convenient casting technique, e.g. by a d.c. casting process, preferably by means of a short mould or hot-top d.c. process.
- the Fe is preferably present as an insoluble secondary phase in the form of fine ⁇ -AIFeSi platelets, preferably not more than 15 ⁇ m in length or, if in the ⁇ form, free from script and coarse eutectic particles.
- the as-cast extrusion ingot is homogenised, partly to bring the soluble secondary magnesium-silicon phases into suitable form, to dissolve the silicon and partly to convert ⁇ -AIFeSi particles into substantially ⁇ -AIFeSi particles, preferably below 15 ⁇ m long and with 90% below 6 ⁇ m long.
- Homogenisation typically involves heating the ingot at more than 530°C e.g. 550 - 600°C for 30 minutes to 24 hours with higher temperatures requiring shorter hold times.
- Cooling from homogenisation temperature should preferably be sufficiently fast to avoid the formation of coarse ⁇ -Mg 2 Si particles which would not redissolve during extrusion. It is preferred to cool the ingot at a rate of at least 150°C per hour from homogenisation temperature down to a temperature not greater than 425°C. The ingot may be held for a few hours at a temperature in the range 300 - 425°C, as described in EP 222 479, in order to encourage the formation of a rather fine precipitate ⁇ '-Mg 2 Si which has the effect of reducing extrusion breakthrough pressure and of redissolving during extrusion so as to permit development of maximum tensile strength in age hardened extrusions. The rate of cooling below 300°C is immaterial.
- the homogenised extrusion ingot is then heated for extrusion.
- the solutionising treatment described in EP 302 623 may be used.
- the initial billet temperature can be chosen to match the pressure capacity of the extrusion press being used.
- the emerging extrusion is cooled, either by water or forced air or more preferably in still air, and subjected to an ageing process in order to develop desired strength and toughness properties.
- Ageing typically involves heating the extrusion to an elevated temperature in the range 150 - 200°C, and holding at that temperature for 1 - 48 hours, with higher temperatures requiring shorter hold times.
- a preferred rate of heating is from 10 - 100°C particularly 10 - 70°C per hour; if the heating rate is too slow, low throughput results in increased costs; if the heating rate is too high, the mechanical properties developed are less than optimum.
- An effect equivalent to slow heating can be achieved by a two-stage heating schedule, with a hold temperature typically in the range of 80 - 140°C, for a time sufficient to give an overall heating rate within the above range. Holding the extrusion for 24 hours or more at room temperature is also beneficial.
- extrusions When aged to peak strength, extrusions are capable of meeting the requirements of T5 (tensile strength of 152 MPa) or preferably of T6 (tensile strength of about 207 MPa) with improved press productivity.
- the reduced flow stress characteristics also make it possible to produce shapes such as high aspect ratio heat sinks that are difficult to produce in existing alloys.
- the basic features of the alloys can also be applied for bright dip applications, with appropriate additions of copper or for matt etching applications with appropriate control of the iron content. Some of the more dilute versions of the alloys are suitable for applications where low strength is acceptable but where good formability is required.
- compositions listed in Tables 1 and 2 were DC cast as 100 mm diameter ingots. These covered the following ranges of composition:
- the range of alloys included a control alloy based on a commercially available alloy 6060 (Example 11) and 6063.
- the billets were homogenised using a practice of 2 hrs at 585°C followed by cooling at 350°C/hr, which is a typical practice for Al- Mg-Si alloys.
- the alloys were then extruded using a 750 tonne, 100 mm diameter extrusion press. Billets were induction heated using a number of different practices and then extruded into a 50 x 3 mm flat strip, equivalent to an extrusion ratio of 52:1.
- the extrusion speeds used ranged from 12 to 40 m/min. Initially the billet was extruded using a billet temperature of 480°C at an exit speed of 40 m/min giving an exit temperature of at least 510°C. The strip was still air cooled at 2°C/sec. After 24 hours the alloys were aged using the following practices:
- the minimum tensile strength requirement of AA6063T6 can be satisfied at magnesium levels of 0.29 and above with appropriate control of the silicon level.
- the strength obtained from such alloys is equivalent to the properties obtained with the alloy 6060.
- the 6063T5 minimum tensile strength requirement can be easily met with all but the lowest Mg and Si compositions tested. This includes all the new 0.25 wt% Mg alloys tested apart from the lowest silicon level.
- Figure 1 showing alloy composition fields and strength contours have been reproduced as Figure 3, in which are shown the compositions and tensile strengths of the various alloys listed in Table 1. From this graph it is evident that alloys containing as little as 0.20 wt% Mg can be formulated with suitably high Si contents to pass the T5 specification.
- Figure 4 is a graph of elongation at break for alloys of various compositions after ageing by practice 1. Elongation at break in a tensile test is one measure of formability. The following conclusions can be drawn from this figure:
- the pressure requirements of the new alloy range have been compared with existing alloys AA6060 and AA6063 in the temperature range 400 to 475°C.
- the alloys were extruded into a thin wall profile (1.3 mm thick l-section) at a reduction ration of 125:1.
- Individual billets were extruded at 400, 425, 450, 475°C.
- the experiments were carried out on a laboratory press as described previously. The press liner, die and tooling were preheated to the billet temperature in each case.
- the AA6063 composition is included in Table 1.
- Figure 5 summarises the results expressed as mean breakthrough pressure over the temperature range 400 - 475°C.
- the alloys are ranked on the y-axis in terms of decreasing magnesium and silicon contents.
- Figures 8 and 9 show the effect of ageing practice on the properties achievable. Further increases in strength are possible for all the compositions studied by reducing the heating rate to the ageing temperature to 20°C/hr (practice 3) or by using the two stage heat treatment (practice 4).
- Figures 10 to 13 show the results of experiments performed by taking 178 mm diameter ingots of alloys according to the invention containing 0.25 - 0.50 wt% magnesium (the Mg content does not affect the results) and variable concentrations of silicon as shown; and subjecting the ingots to homogenisation under conventional conditions, typically 2 hours at 585°C.
- Figure 10 shows the effect of increasing silicon levels on the percentage of ⁇ -AIFeSi remaining after homogenisation for ingots containing 0.03 wt% Mn. Above 0.5 wt% Si, the percent ⁇ -AIFeSi at the end of homogenisation is significantly reduced.
- Figures 11 and 12 show the mean size and degree of spheroidisation for the same alloys. The increase in residual ⁇ -AIFeSi at higher Si levels corresponds to an increase in particle size and lack of spheroidisation.
- a single further point shows that, by changing the Mn concentration from 0.03% to 0.09%, these detrimental effects on intermetalllic type, size and shape can be reversed.
- Figure 13 shows the effect of incremental Mn additions on the level of ⁇ -AIFeSi remaining after standard homogenisation practice. Lines are shown for two Si levels of 0.50% and 0.60%.
- a target often used for homogenisation of dilute 6060 alloys is to achieve 90% ⁇ -AIFeSi after homogenisation.
- the amount of Mn required to achieve this increases with the bulk Si content.
- a deliberate addition of Mn is not necessary to achieve this target, but the addition can still be useful in improving the extent of spheroidisation for a given homogenisation treatment.
- Figure 14 is a graph showing the effect of Mg and Si content on roughness Ra of extrusions made from alloys shown in Table 1 at an extrusion temperature of 450°C.
- the exit speed was 100 m/min
- the extrusion ratio was 125:1
- the section thickness was 1.3 mm. It can be seen that surface roughness begins to be a problem at Si levels above about 0.52 wt%.
- Figure 15 is a chart showing the effect of alloy composition on tensile strength. Four ingots of each of nine different alloy compositions 17 to 25 as shown in Table 3 were extruded and aged and the UTS measured. The billet temperature was 450°C, the extrusion ratio was 125:1 and the quench rate was 3°C/s.
- Table 4 below provides further data on the extrusion properties of those example alloys 17 to 25: the load required to achieve extrusion at 100 metres/minute; and the roughness of the resulted extruded section.
- a comparison of example alloys 18, 19 and 20 shows that, at high Si levels, surface finish can be substantially improved by Mn addition.
- a comparison of prior art alloys 21 and 25 with the others shows that the invention alloys require lower extrusion pressures.
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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)
- Extrusion Of Metal (AREA)
Abstract
Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP98912599A EP0968315B1 (en) | 1997-03-21 | 1998-03-20 | Al-Mg-Si ALLOY WITH GOOD EXTRUSION PROPERTIES |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP97301911 | 1997-03-21 | ||
EP97301911 | 1997-03-21 | ||
PCT/GB1998/000849 WO1998042884A1 (en) | 1997-03-21 | 1998-03-20 | Al-Mg-Si ALLOY WITH GOOD EXTRUSION PROPERTIES |
EP98912599A EP0968315B1 (en) | 1997-03-21 | 1998-03-20 | Al-Mg-Si ALLOY WITH GOOD EXTRUSION PROPERTIES |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0968315A1 true EP0968315A1 (en) | 2000-01-05 |
EP0968315B1 EP0968315B1 (en) | 2001-11-14 |
Family
ID=26147353
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP98912599A Revoked EP0968315B1 (en) | 1997-03-21 | 1998-03-20 | Al-Mg-Si ALLOY WITH GOOD EXTRUSION PROPERTIES |
Country Status (2)
Country | Link |
---|---|
EP (1) | EP0968315B1 (en) |
WO (1) | WO1998042884A1 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10215188B4 (en) * | 2002-04-05 | 2005-12-08 | Carl Mahr Holding Gmbh | Measuring guide device with linear guide |
NO20034731D0 (en) | 2003-10-22 | 2003-10-22 | Norsk Hydro As | aluminum Alloy |
WO2011105584A1 (en) * | 2010-02-26 | 2011-09-01 | 古河電気工業株式会社 | Aluminum alloy conductor |
WO2021254852A1 (en) | 2020-06-15 | 2021-12-23 | Dimitri Fotij | Reliable high extrusion rate production method for high corrosion resistance powdercoated recycle friendly aluminum soft alloys |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1333327A (en) * | 1971-05-25 | 1973-10-10 | Alcan Res & Dev | Aluminium alloys |
JPH02200750A (en) * | 1989-01-31 | 1990-08-09 | Sumitomo Light Metal Ind Ltd | Aluminum alloy stock excellent in electric conductivity and its production |
GB9318041D0 (en) * | 1993-08-31 | 1993-10-20 | Alcan Int Ltd | Extrudable a1-mg-si alloys |
-
1998
- 1998-03-20 EP EP98912599A patent/EP0968315B1/en not_active Revoked
- 1998-03-20 WO PCT/GB1998/000849 patent/WO1998042884A1/en not_active Application Discontinuation
Non-Patent Citations (1)
Title |
---|
See references of WO9842884A1 * |
Also Published As
Publication number | Publication date |
---|---|
WO1998042884A1 (en) | 1998-10-01 |
EP0968315B1 (en) | 2001-11-14 |
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