WO2008144935A1 - Aluminum alloy formulations for reduced hot tear susceptibility - Google Patents

Aluminum alloy formulations for reduced hot tear susceptibility Download PDF

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Publication number
WO2008144935A1
WO2008144935A1 PCT/CA2008/001051 CA2008001051W WO2008144935A1 WO 2008144935 A1 WO2008144935 A1 WO 2008144935A1 CA 2008001051 W CA2008001051 W CA 2008001051W WO 2008144935 A1 WO2008144935 A1 WO 2008144935A1
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alloy
aluminum
weight
solid
semi
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PCT/CA2008/001051
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English (en)
French (fr)
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Joseph Langlais
Alain Lemieux
Neivi Andrade
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Alcan International Limited
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Priority to JP2010509649A priority Critical patent/JP2010528187A/ja
Priority to EP08757187A priority patent/EP2152923A4/de
Priority to CA002687893A priority patent/CA2687893A1/en
Publication of WO2008144935A1 publication Critical patent/WO2008144935A1/en

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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22DCASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
    • B22D17/00Pressure die casting or injection die casting, i.e. casting in which the metal is forced into a mould under high pressure
    • B22D17/007Semi-solid pressure die casting
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22DCASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
    • B22D21/00Casting non-ferrous metals or metallic compounds so far as their metallurgical properties are of importance for the casting procedure; Selection of compositions therefor
    • B22D21/002Castings of light metals
    • B22D21/007Castings of light metals with low melting point, e.g. Al 659 degrees C, Mg 650 degrees C
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C1/00Making non-ferrous alloys
    • C22C1/02Making non-ferrous alloys by melting
    • C22C1/026Alloys based on aluminium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C1/00Making non-ferrous alloys
    • C22C1/02Making non-ferrous alloys by melting
    • C22C1/03Making non-ferrous alloys by melting using master alloys
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C1/00Making non-ferrous alloys
    • C22C1/06Making non-ferrous alloys with the use of special agents for refining or deoxidising
    • 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
    • C22CALLOYS
    • C22C21/00Alloys based on aluminium
    • C22C21/06Alloys based on aluminium with magnesium as the next major constituent
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C21/00Alloys based on aluminium
    • C22C21/06Alloys based on aluminium with magnesium as the next major constituent
    • C22C21/08Alloys based on aluminium with magnesium as the next major constituent with silicon
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C21/00Alloys based on aluminium
    • C22C21/12Alloys based on aluminium with copper as the next major constituent
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C21/00Alloys based on aluminium
    • C22C21/12Alloys based on aluminium with copper as the next major constituent
    • C22C21/14Alloys based on aluminium with copper as the next major constituent with silicon
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C21/00Alloys based on aluminium
    • C22C21/12Alloys based on aluminium with copper as the next major constituent
    • C22C21/16Alloys based on aluminium with copper as the next major constituent with magnesium

Definitions

  • the invention relates to modified alloy compositions for reduced hot tear susceptibility.
  • Hot tears occur during casting wherein brittle interdendritic fractures initiate during the solidification process. Alloys which are generally considered to be prone to hot tearing have relatively long freezing/solidification ranges, defined as the temperature difference between the liquidus and solidus temperatures. In addition, during the final stages of freezing, these alloys have very little eutectic liquid remaining, and the limited amounts of this eutectic liquid must pass through narrow spaces left between the solidified grains. This poor feeding in the final stages of solidification is a significant contributor to the phenomenon of hot tearing.
  • WO2005/056846 A method of reducing hot tearing is disclosed in WO2005/056846.
  • WO2005/056846 is silent to the combination of strontium and titanium diboride of the present invention and primarily addresses the problem of hot tearing by casting a mix of a pure aluminum at a first specified temperature and a second aluminum alloy mixed with copper, zinc, or magnesium at a second specified temperature. Temperature control of the two alloys is a central aspect of the method disclosed in WO2005/056846.
  • US 4,681,152 is directed to twin roll casting of an 5xxx alloy.
  • the composition can contain up to 0.05% Sr and uses a grain refiner comprising aluminum wire containing about 5% by weight titanium and 0.2% by weight boron.
  • the boron content can be as much as 1% by weight.
  • Sufficient grain refining alloy is added to bring the titanium content up to about 0.02% by weight.
  • US 4,681,152 is not directed to reducing hot tearing.
  • US 5,453,244 is directed to a bearing alloy including Al-Zn base (7xxx) .
  • the alloy is broadly described as containing 0.05 to 0.5% Sr and Ti+B in the range 0.03 to 0.5%.
  • US 5,453,244 is not directed to reducing hot tearing.
  • US 5,211,910 mentions Sr from a list consisting of Zn, Ge, Sn, Cd, In, Be, Sr, Sc, Y, and Ca to be present in about 0.5 to about 4 weight percent total and Ti and/or TiB 2 from a list comprising Zr, Cr, Mn, Ti, Hf, V, Nb, B and TiB 2 in the range 0.01 to 2% as constituents of 2xxx alloy.
  • Sr from a list consisting of Zn, Ge, Sn, Cd, In, Be, Sr, Sc, Y, and Ca to be present in about 0.5 to about 4 weight percent total
  • Ti and/or TiB 2 from a list comprising Zr, Cr, Mn, Ti, Hf, V, Nb, B and TiB 2 in the range 0.01 to 2% as constituents of 2xxx alloy.
  • US 5,211,910 is not directed to reducing hot tearing.
  • EP0432184 mentions Sr from a list consisting of Zn, Ge, Sn, Cd, In, Be, Sr, Sc, Y, and Ca to be present in about 0.01 to 1.5 and Ti and/or TiB 2 from a list comprising Zr, Cr, Mn, Ti, Hf, V, Nb, B and TiB 2 in the range 0.01 to 1.5%.
  • Sr from a list consisting of Zn, Ge, Sn, Cd, In, Be, Sr, Sc, Y, and Ca to be present in about 0.01 to 1.5
  • Ti and/or TiB 2 from a list comprising Zr, Cr, Mn, Ti, Hf, V, Nb, B and TiB 2 in the range 0.01 to 1.5%.
  • EP0432184 is not directed to reducing hot tearing.
  • WO 96/10099 discloses a broad range of possible alloys, and includes grain refiners (including Ti and TiB 2 ) and modifiers (including Sr) .
  • US 6,562,165 describes an Al-Si alloy suitable for semi-solid processing containing Ti 0.005 to 0.5% and Sr 0.005 to 0.030, with spheroidized structure. US 6,562,165 mentions that excessive Ti addition can lead to large, detrimental TiB 2 crystals and is silent to TiB 2 levels. The additives of US 6,562,165 are not intended to reduce hot tearing.
  • the inventors have found that aluminum-based alloys comprising as additives a narrowly specified range of both strontium and titanium diboride have surprisingly low incidences of hot tearing, thereby allowing die casting of these alloys.
  • the present invention is directed to a modified alloy composition applicable to aluminum alloys to control hot tearing by the selective use of additives, thereby providing for these alloys to be subject to die casting, wherein the alloys of the invention have a strength and ductility properties absent in conventional aluminum alloys. These properties allow for shape casting of either above the liquidus of the alloy or in the semi-solid region of the alloy. - A -
  • the strontium and titanium diboride additives work in a synergistic manner on the alloy, wherein the strontium promotes the formation of spheroidal grains in the alpha grains and the titanium diboride initiates the formation of new grains.
  • these alloying components allow the liquid aluminum based alloy to flow until the final solidification, thereby preventing or significantly reducing the incidence of hot tearing.
  • a first aspect of the invention is directed to an aluminum alloy comprising i) from 0.010 to 0.025% by weight Sr,- and ii) TiB 2 , measured by its boron content, from 0.001 to 0.005% by weight B.
  • the aluminum alloy further comprises iii) 0.16% or less of excess Ti over the amount bound stoichiometrically with the B in TiB 2 . It has been found that a number of alloys normally susceptible to hot tearing are highly suitable to the use of the additives of the invention in their specified ranges.
  • a related aspect of the invention relates to a method of preventing or eliminating hot tears in an aluminum alloy comprising the step of combining with aluminum i) from 0.010 to 0.025% by weight Sr,- and ii) TiB 2 , measured by its boron content, from 0.001 to 0.005% by weight B.
  • a further object of the invention is to provide a shape cast part, cast from an alloy defined by the present invention.
  • the shape cast may be a die cast, which is difficult with hot tearing susceptible aluminum alloys.
  • Further advantages are provided by the present invention in that the cast from the alloy may be in a semi-solid state.
  • the invention may be alternatively defined as providing a method of providing an aluminum alloy comprising combining with aluminum i) from 0.010 to 0.025% by weight Sr and ii) TiB 2 , measured by its boron content, from 0.001 to 0.005% by weight B.
  • a particularly interesting aspect of the invention relates to a method for processing an aluminum alloy said aluminum alloy having i) from 0.010 to 0.025% by weight Sr and ii) TiB 2 , measured by its boron content, from 0.001 to 0.005% by weight B, and said alloy having a liquidus temperature and a solidus temperature, the method comprising the steps of providing the alloy having a semi-solid range between the liquidus temperature and the solidus temperature of the alloy,- heating the alloy to an alloy initial elevated temperature above the liquidus temperature to fully melt the alloy; reducing the temperature of the alloy from the initial metallic alloy elevated temperature to a semi-solid temperature of less than the liquidus temperature and more than the solidus temperature; maintaining the alloy at the semi -solid temperature for a sufficient time to produce a semi -solid structure in the alloy of a globular solid phase dispersed in a liquid phase.
  • the invention relates to aluminum based alloys.
  • the aluminum based alloys may be selected from the group consisting of alloys comprising primarily of aluminum and copper such as of the 2xxx and 2xx type; alloys comprising primarily of aluminum and manganese such as of the 3xxx type; alloys comprising primarily of aluminum and silicon such as of the 4xxx type; alloys comprising primarily of aluminum and magnesium such as of the 5xxx and 5xx type; alloys comprising primarily of aluminum, magnesium and silicon such as of the 6xxx type; and alloys comprising primarily of aluminum and zinc such as of the 7xxx type.
  • the term "primarily" in the context of the alloys of the present invention is intended to mean that these elements provide the highest weight content in the alloy, with aluminum being the highest contributor to the weight content .
  • the aluminum alloys of the present invention comprise the unique combination of strontium and titanium diboride, namely i) from 0.010 to 0.025% by weight Sr and ii) TiB 2 , measured by its boron content, from 0.001 to 0.005% by weight B.
  • TiB 2 is a known grain refiner, in this specific combination of this specified grain refiner with strontium, the liquid alloy left in the solidifying alloy is not flow restricted.
  • Titanium, zirconium and their borides and carbides are all known grain refiners. Surprisingly, titanium diboride when used in combination with strontium, a crystal modifier, gave surprising improvements to the properties of the aluminum alloy preventing or eliminating the incidence of hot tearing .
  • the aluminum alloy further comprises 0.16% or less by weight excess Ti and more preferably 0.12% or less by weight excess Ti. By excess Ti, we mean the amount of Ti over that which forms TiB 2 .
  • the Ti can be introduced by a number of manners known to the skilled person, it is typically introduced either by the addition of metallic titanium or through the use of a "grain refiner" rod, which is an aluminum rod or wire containing specified levels of Ti and B with a stoichiometry designed to generate TiB 2 with an excess of Ti, as known by the skilled person.
  • a "grain refiner" rod which is an aluminum rod or wire containing specified levels of Ti and B with a stoichiometry designed to generate TiB 2 with an excess of Ti, as known by the skilled person.
  • the aluminum alloy of the invention may comprise additives in addition to strontium and titanium diboride, and optionally titanium, for a wide range of purposes such as Mg, Cu and Zn for strength, Mn and Fe for strength and reduction of die soldering in die casting, and Ca, Na and Sb for grain modification.
  • the invention is directed to an alloy comprising TiB 2 (measured by its boron content) from 0.001 to 0.005% by weight B, preferably from 0.002 to 0.004% by weight TiB 2 (measured by its boron content) .
  • the invention relates to an aluminum alloy comprising from 0.010 to 0.025% by weight Sr, preferably 0.010% to 0.020% by weight Sr.
  • the use of excess titanium is not advantageous in terms of the controlling the hot tearing effect as it contributes to the formation of excessively large and elongated grains.
  • Excess Ti has a negative effect on hot tearing and, if in excess of 0.16%, results in the formation of Al-Ti intermetallics which are acicular and contribute to hot tearing as well as increasing the brittleness of the cast product.
  • the alloys of the present invention have preferably 0.16% or less by weight excess Ti, more preferably 0.12% or less by weight excess Ti.
  • the additives of the invention are highly suited to an aluminum alloy comprising primarily aluminum, magnesium, and silicon. Accordingly, an interesting embodiment of the invention relates to an aluminum alloy compirising primarily of aluminum, magnesium, and silicon and further comprising 0.010 to 0.025% by weight Sr, and TiB 2 (measured by its boron content) from 0.001 to 0.005% by weight B. A further interesting embodiment of the invention relates to an aluminum alloy comprising primarily of aluminum, magnesium, and silicon and 0.010 to 0.025% by weight Sr, TiB 2 (measured by its boron content) from 0.001 to 0.005% by weight B and preferably 0.16% or less by excess Ti over the amount bound stoi.chiometrically with the B in TiB 2 .
  • an interesting embodiment of the invention relates to an aluminum alloy comprising primarily of aluminum and copper and further comprising 0.010 to 0.025% by weight Sr, and TiB 2 (measured by its boron content) from 0.001 to 0.005% by weight B.
  • an aluminum alloy comprising primarily of aluminum, and copper and 0.010 to 0.025% by weight Sr, TiB 2 (measured by its boron content) from 0.001 to 0.005% by weight B and preferably 0.16% or less by excess Ti over the amount bound stoichiometrically with the B in TiB 2 .
  • the additives of the invention are highly suited to an aluminum alloy comprising primarily aluminum and magnesium. Accordingly, an interesting embodiment of the invention relates to an aluminum alloy comprising primarily of aluminum and magnesium and further comprising 0.010 to 0.025% by weight Sr, and TiB 2 (measured by its boron content) from 0.001 to 0.005% by weight B. In a further interesting embodiment of the invention relates to an aluminum alloy comprising primarily of aluminum and magnesium and 0.010 to 0.025% by weight Sr, TiB 2 (measured by its boron content) from 0.001 to 0.005% by weight B and preferably 0.16% or less by weight excess Ti over the amount bound stoichiometrically with the B in TiB 2 .
  • alloys are referred to by the International Alloy Designations of the Aluminum Association.
  • a 2xxx alloy therefore refers to a wrought alloy that is principally aluminum with Cu as the main alloying element (where the Cu may be present, for example, up to about 7 percent by weight)
  • a 2xx alloy therefore refers to a foundry alloy that is principally aluminum with Cu as the main alloying element (where the Cu may be present, for example, up to about 9 percent by weight) .
  • An example of an aluminum Cu alloy would be the 206 alloy, which has a composition in weight percent of Si less than 0.1, Fe less than 0.15, Cu 4.2 to 5.0, Mn 0.20 to 0.50, Mg 0.15 to 0.35, Ni less than 0.05, Zn less than 0.10, Sn less than 0.05, balance Al with incidental impurities each less than 0.05 and total less than 0.15, plus 0.010 to 0.025% by weight Sr, TiB 2 (measured by its boron content) from 0.001 to 0.005% by weight B, and preferably 0.16% or less by weight excess Ti over the amount bound stoichiometrically with the B in TiB 2 .
  • an aluminum Cu alloy would be the 2024 alloy, which has a composition in weight percent of Si less than 0.5, Fe less than 0.5, Cu 3.8 to 4.9, Mn 0.30 to 0.9, Mg 1.2 to 1.8, Cr less than 0.10, Zn less than 0.25, balance Al with incidental impurities each less than 0.05 and total less than 0.15, plus 0.010 to 0.025% by weight Sr, TiB 2 (measured by its boron content) from 0.001 to 0.005% by weight B and preferably 0.16% or less by excess Ti over the amount bound stoichiometrically with the B in TiB 2 .
  • a 3xxx alloy refers to a wrought alloy that is principally aluminum with Mn as the main alloying element up to about 1.5 percent by weight.
  • a 4xxx alloy refers to a wrought alloy that is principally aluminum with Si as the main alloying element up to about 14 percent by weight.
  • a 5xxx alloy refers to a wrought alloy that is principally aluminum with Mg as the main alloying element up to about 6 percent by weight.
  • a 5xx alloy refers to a foundry alloy that is principally aluminum with Mg as the main alloying element up to about 11 percent by weight.
  • An example of an aluminum Mn alloy would be the 5182 alloy, which has a composition in weight percent of Si less than 0,2, Fe less than 0.35, Cu less than 0.15, Mn 0.20 to 0.50, Mg 4.0 to 5.0, Cr less than 0.1, Zn less than 0.25, balance Al with incidental impurities each less than 0.05 and total less than 0.15, plus 0.010 to 0.025% by weight Sr, TiB 2 (measured by its boron content) from 0.001 to 0.005% by weight B and preferably 0.16% or less by excess Ti over the amount bound stoichiometrically with the B in TiB 2 .
  • a 6xxx alloy refers to a wrought alloy that is principally aluminum with Mg and Si as the main alloying elements with Mg present up to about 1.6 percent by weight and Si present up to about 1.7 percent by weight and where magnesium suicide forms during solidification.
  • An example of an aluminum Mg-Si alloys would be 6061 alloy, which has a composition in weight percent of Si 0.40 to 0.80, Fe less than 0.7, Cu 0.15 to 0.40, Mn less than 015, Mg 0.8 to 1.2, Cr 0.04 to 0.35, Zn less than 0.25, balance Al with incidental impurities each less than 0.05 and total less than 0.15, plus 0.010 to 0.025% by weight Sr, 0.005 to 0.025% by weight TiB 2 (measured by its boron content) from 0.001 to 0.005% by weight B and preferably 0.16% or less by excess Ti over the amount bound stoichiometrically with the B in TiB 2 .
  • a 7xxx alloy refers to a wrought alloy that is principally aluminum with Zn as the main alloying element, typically present up to about 9 percent by weight.
  • alloys would have, in addition to the elements , named, TiB 2 , Sr, and optionally Ti in the ranges stated above to give reduced hot tearing. These alloys may also contain additional alloying elements including Si, Fe, Cu, Mn, Mg, Cr, Ni, Zn, and V.
  • the additives of the present invention namely 0.010 to 0.025% by weight Sr, and TiB 2 (measured by its boron content) from 0.001 to 0.005% by weight B, are also considered to be highly suitable for 2xxx and 2xx aluminum- copper alloys.
  • 2xxx and 2xx Al-Cu alloys are known to be crack prone.
  • the Sr and TiB 2 additives in their stated amounts allow for die casting of 2xxx and 2xx alloys and thereby allowing for complex part shapes and designs.
  • By controlling hot tearing in aluminum-copper alloys (2xxx and 2xx alloys) it has been possible to die cast 2xxx and 2xx alloys, which is normally difficult using conventional alloys.
  • the alloys of the invention retain strength and ductility properties similar to the unmodified alloys even though die cast.
  • the alloy is cast, such as shape cast or die cast.
  • alloys comprising primarily of aluminum and magnesium such as of the 5xxx and 5xx type are known to be crack prone.
  • the use of 0.010 to 0.025% by weight Sr, and TiB 2 (measured by its boron content) from 0.001 to 0.005% by weight B in aluminum and magnesium such as of the 5xxx and 5xx type allow for die casting of 5xxx and 5xx alloys and thereby allowing for complex part shapes and designs.
  • By controlling hot tearing in alloys comprising primarily of aluminum and magnesium such as of the 5xxx and 5xx type it has been possible to die cast 5xxx and 5xx alloys, which is normally difficult using conventional alloys.
  • the alloys of the invention retain strength and ductility properties similar to the unmodified alloys even though die cast.
  • the alloy is cast, such as shape cast or die cast .
  • the alloy formulations of the invention are suitable for use in any number of shape casting processes including, but not limited to, sand casting, permanent mold casting, and die casting.
  • Example processes would include gravity permanent mold, low pressure permanent mold, and vacuum permanent mold.
  • high pressure diecasting processes including both conventional high pressure diecasting and high integrity diecasting processes such as high-vacuum diecasting, semi-solid forming, and squeeze casting.
  • Hot tearing is not, of course, a phenomenon unique to the shape casting of near-net shape parts but is also a limitation frequently encountered when casting billets, blooms, or T-Ingot cross sections via either semi-continuous or continuous casting processes (e.g. direct-chill casting or horizontal continuous casting) .
  • the formulations of the invention are, of course, applicable to the reduction in hot tear susceptibility when casting these types of products as well .
  • by controlling hot tearing in Al-Mg-Si alloys (6xxx alloys) it has been possible to die cast 6xxx alloys, which is normally difficult using conventional alloys.
  • the alloys of the invention retain the strength and ductility properties of the unmodified alloys even when die cast and provide properties normally absent in conventional aluminum shape casting alloys.
  • the alloy is cast, such as shape cast or die cast .
  • the casting can be done at either above the liquidus of the alloy or in the semi-solid region.
  • the present invention is directed, in one embodiment, to casting in the semi-solid region since it has been found that not only is hot tearing resistance observed, this gives further improvements in die filling and general suitability for casting.
  • the semi-solid structure may have a globular solid phase under certain processing conditions and this is particularly favourable for casting.
  • the casting of the alloy of the invention into a useful shape starting from a temperature above the liquidus (where the alloy is fully molten) can be done by any technique known to those skilled in the art.
  • a particularly preferred 6xxx alloy for casting by semi-solid or fully molten processes has a composition in weight percent of Si 0.6 to 0.8, Fe up to 0.12, Cu 0.15 to 0.40, Mg 0.8 to 1.2, Cr 0.04 to 0.10, Sr 0.006 to 0.025, 0.005 to 0.025% by weight TiB 2 (measured by its boron content) from 0.001 to 0.005% by weight B and preferably 0.16% or less by excess Ti over the amount bound stoichiometrically with the B in TiB 2 .
  • the particularly preferred 6xxx alloy balance Al with incidental impurities each less than 0.05 and total less than 0.15, whereas for processing in the fully molten state the particularly preferred 6xxx alloy will have additionally up to 0.45% by weight Mn, provided that the total Mn+Fe is between 0.55 to 0.65% by weight, balance Al with incidental impurities each less than 0.05 and total less than 0.15.
  • Semi-solid processing can beneficially use lower levels of Fe and Mn since the process is less susceptible to die-sticking. For processing above the liquidus, control of the total Fe+Mn is advantageous to reduce die sticking.
  • a solid rod or ingot that may have been specially cast to have a fine globular structure in the solid phase is reheated to a temperature between the solidus and liquidus temperatures and then transferred to a shape casting mould.
  • a fully liquid alloy is cooled to a temperature between the liquidus and solidus temperature to create a semi-solid slurry which is then cast.
  • the process is controlled to ensure that the solid fraction has a globular rather than dendritic structure. This may be accomplished by rapid cooling, optionally with the addition of solid nuclei, or by vigorous agitation (e.g. electromagnetic stirring) during cooling to a predefined temperature.
  • the semi-solid mixture may be held at this temperature (for a few seconds to several minutes) to allow the solid particles to grow into globular structures.
  • the semi-solid slurry having a globular structure is generally thixotropic which enhances its mould filling capabilities.
  • the vessel in which the slurry is formed may be heated and/or cooled by external means to ensure that the correct predefined temperature is maintained.
  • the temperature and weight of the fully liquid alloy is adjusted so that when it is added to a vessel of known mass, heat capacity and temperature, the alloy attains the desired predefined temperature in the semi-solid region and stabilizes there for a period of time to permit globularization of the structure.
  • some of the unsolidified liquid alloy may be removed (e.g. by draining through a filter or orifice) during or after the period at the predefined temperature. This achieves a further improvement in the structure of the semi-solid alloy and permits easier removal of the semi -solid material to the casting machine.
  • the semi -solid slurry after preparation may be cast by known shape casting techniques. Die casting is a particularly preferred technique.
  • the present invention provides aluminum alloys with reduced incidences of hot tearing.
  • the combination of modifiers and grain refiner addition controls both the primary alpha and secondary phases of the alloy.
  • the high degree of control of the grain size and morphology provided by the present invention is achieved using a narrow range of titanium diboride, preferably well distributed within the melt.
  • a high control of the primary alpha phase allows for the eutectic liquid to move more freely (compared to in the absence of titanium diboride) within the solidifying network.
  • the precipitation of the secondary phase comprising the intermetallics (such as Mg 2 Si in 6xxx alloys) is considered to affect the flow of the eutectic liquid between the globular structures and prevent feeding of any incipient hot tears.
  • the grain refiners and modifiers control the size and morphology of both the secondary and primary phases.
  • the primary alpha phase is generally the last phase to form during solidification
  • the present invention in particular controls the size and shape of the alpha phase to ensure that the eutectic liquid is free to move in the solidifying network.
  • the secondary phase between the alpha grains affects the flow of eutectic fluid and therefore refinement and modification of the secondary phase is also important to ensure adequate alloy feeding and prevention of incipient hot tears.
  • Samples of two base alloys of the Al-Mg-Si type, two of the Al-Cu and one of the Al-Mg type were prepared as follows (compositions in weight percent)
  • C is the assigned numerical value for the severity of the crack in the bars
  • L is the assigned numerical value corresponding to the length of the bar
  • the boron is present as TiB 2 .
  • Total Ti is the total amount of Ti from all sources and Ti (excess) is the amount of Ti that is not bound up in TiB 2 .
  • Alloys A15 to A19, B7 to B12, ClO to C19, D9 to D18 and ElO to E18 represent alloys within the inventive range of additives, whereas the remaining alloys are outside the range. Alloys Al, Bl, Cl, Dl and El represent the base alloys with no additive elements.
  • the Hot Tearing Susceptibility Index for the alloys within the inventive range is less than those outside the range. The change is sufficient that in actual castings the presence of cracks due to hot tearing in the inventive alloys is substantially reduced.
  • Samples were produced using both a liquid alloy die casting process and the preferred semi-solid process described above, in which a mass of alloy above the liquidus was cooled rapidly to a temperature in the semi-solid region, the temperature determined by the relative masses and temperatures of the alloy and holding crucible, holding the mass of metal for a period of time then draining a portion of the remaining liquid from the crucible before casting.
  • the amount of liquid alloy drained from the semisolid mass prior to casting was from 15 to 18% .
  • the cast parts were heat treated by two different processes.
  • Treatment I Heat Treatment: 3 h @ 530 0 C + Quench + 18 h @ 160 0 C.
  • Treatment II Heat Treatment: 3 h @ 530 0 C + Quench + 8 h @ 170 0 C.
  • Liquid die penetrant analysis was used to determine a hot tearing index for the cast parts.
  • the straight side sections of the U shape was examined and a hot tearing index determined for these locations.
  • Tensile tests were run on samples cut from the same locations.
  • the hot tearing index is a semi -quantitative index which assigned a score for each defect found in the locations examined.
  • a score of 0 means no defect
  • a score of 1 means a point defect (no propagation)
  • a scope of 2 means propagation length less than or equal to the width of the side section
  • a score of 3 means propagation length greater than che with of the side section.
  • the Index was the sum of these scores for four locations along the straight side sections of the U shape .
  • Die cast parts were prepared from the inventive alloy A16. Samples were produced using the preferred semi-solid process described above, in which a mass of alloy above the liquidus was cooled rapidly to a temperature in the semisolid region, the temperature determined by the relative masses and temperatures of the alloy and holding crucible, holding the mass of metal for a period of time without draining any remaining liquid from the crucible before casting. The cast parts were heat treated by the following process .
  • Treatment III Heat Treatment: 8 h @ 540 0 C + Quench + 6 h @ 170 0 C.
  • results indicate a lower hot tearing susceptibility for the inventive alloy A16 compared to the base alloy Al. Moreover, results confirm that this inventive alloy A16 has elasticity limits and mechanical strengths in orders of 5 to 10% above the typical values of the 6061 wrought alloy. Also, from fatigue test performed, the inventive alloy A16 in semi-solid has a fatigue life length similar to the 6061 wrought alloy.

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PCT/CA2008/001051 2007-05-31 2008-05-29 Aluminum alloy formulations for reduced hot tear susceptibility WO2008144935A1 (en)

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JP2010509649A JP2010528187A (ja) 2007-05-31 2008-05-29 熱間割れ感受性を減じるためのアルミニウム合金配合物
EP08757187A EP2152923A4 (de) 2007-05-31 2008-05-29 Aluminiumlegierungsformulierungen für verminderte wärmerissanfälligkeit
CA002687893A CA2687893A1 (en) 2007-05-31 2008-05-29 Aluminum alloy formulations for reduced hot tear susceptibility

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CA2687893A1 (en) 2008-12-04

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