CN108971456A - The system and method that transition metal during stablizing primary solidification in cast aluminium alloy gold precipitates - Google Patents

The system and method that transition metal during stablizing primary solidification in cast aluminium alloy gold precipitates Download PDF

Info

Publication number
CN108971456A
CN108971456A CN201810474172.0A CN201810474172A CN108971456A CN 108971456 A CN108971456 A CN 108971456A CN 201810474172 A CN201810474172 A CN 201810474172A CN 108971456 A CN108971456 A CN 108971456A
Authority
CN
China
Prior art keywords
melt
temperature
aluminium
chamber
precipitating
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.)
Pending
Application number
CN201810474172.0A
Other languages
Chinese (zh)
Inventor
H·W·多蒂
D·R·赫斯
Q·王
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
GM Global Technology Operations LLC
Original Assignee
GM Global Technology Operations LLC
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 GM Global Technology Operations LLC filed Critical GM Global Technology Operations LLC
Publication of CN108971456A publication Critical patent/CN108971456A/en
Pending legal-status Critical Current

Links

Classifications

    • 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
    • B22D21/02Casting exceedingly oxidisable non-ferrous metals, e.g. in inert atmosphere
    • B22D21/04Casting aluminium or magnesium
    • 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
    • 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
    • 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
    • C22C21/02Alloys based on aluminium with silicon as the next major constituent

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Continuous Casting (AREA)
  • Silicon Compounds (AREA)

Abstract

System for cast aluminium alloy gold includes the first chamber for accommodating the first melt for being in the first temperature, for accommodating the second chamber for being in the second melt of the second temperature lower than the first temperature, it is connected to first chamber and second chamber and is used to receive the first melt from first chamber and the second melt from second chamber and the mixing chamber being mixed simultaneously, and be connected to and be used to receive the mold of blend melt with mixing chamber.

Description

Stablize the transition metal precipitating during primary solidification in cast aluminium alloy gold system and Method
Technical field
The present invention relates to a kind of system and method for the transition metal precipitating during stable primary solidification in cast aluminium alloy gold.
Background technique
Context of the invention is totally presented in the introduction.The inventor referred at present is in the range described in this introduction It works and otherwise can not neither express as the various aspects of the description of the prior art when submitting and also do not imply that ground It is recognized as the prior art of the invention.
Because of good castability, corrosion resistance, machining property and high strength-weight ratio, so ceralumin is in vapour It is had a wide range of applications in the structure member of vehicle, aerospace and common engineering industry.About castability, have compared with low silicon content Alloy composite be considered inherently generating poor casting due to wider freezing range and reduced latent heat.It is lower Silicon alloy is difficult to cast, they have the less mobility for filling mold and lower to supply the latent of solidification shrinkage Heat.In addition, lower silicon alloy is prone to hot tear crack defect in process of setting, the casting of part solidification is because of cooling When casting shrink and tear itself, this, which can leave, may cause leakage, reduced mechanical performance and reduced fatigue life Crack.Due to these manufacturing issues, so transition metal is added into metal composites can aggravate castability and fatigue behaviour.
Alternatively, have the alloy composite compared with high silicon content to be increasingly difficult to be machined, and due to it is rougher just Grade silicon particle and have lower ductility and fracture toughness.In general, the casting character of aluminium alloy depends on several factors, Including technique or heat treatment after composition of alloy, casting and curing condition and casting.
It is attempting to expand or improve purposes of the aluminium alloy in the other application that can obtain benefit provided by aluminium alloy When, existing aluminium alloy casting composition and technique fail in high temperature application.The aluminium of silicon with about 7 to 10 weight percent Alloy is believed to be helpful in casting technique.Silicon expands in process of setting, which compensates alloy during solidification always shrink it is some, Make alloy that there are more energy, increases the mobility of melt to improve the filling of mold, and casting is not usually than including silicon Those of casting preferably solidify.However, the presence of silicon can poison or reduce the energy that alloy forms high-temperature-phase in aluminium alloy melt Power.It reduce the abilities that these alloys are used for the application of some high temperature.The reduction of high-temperature-phase reduces casting in high temperature application Durability.
Summary of the invention
In an illustrative aspect, the system for cast aluminium alloy gold includes being in the first of the first temperature for accommodating The first chamber of melt, for accommodating the second chamber for being in the second melt of the second temperature lower than the first temperature, with first Chamber is connected to second chamber to be used for while receiving the first melt from first chamber and the second melt from second chamber And the mixing chamber being mixed, and the mold of blend melt is connected to and is used to receive with mixing chamber.
In another illustrative aspect, the first melt includes aluminium and at least one peritectoid transition metal element.
In another illustrative aspect, the first melt includes zirconium, scandium, cobalt, chromium, niobium, tantalum, titanium, vanadium, tungsten, molybdenum, hafnium and boron One of.
In another illustrative aspect, the second melt has the combination of the silicon than the first melt comprising greater percentage Object.
In another illustrative aspect, the second melt has the combination of the copper than the first melt comprising greater percentage Object.
In another illustrative aspect, the second melt has the combination of the magnesium than the first melt comprising greater percentage Object.
In another illustrative aspect, the first temperature is higher than the liquidus temperature of aluminum precipitation in the first melt, the second temperature Liquidus temperature of the degree lower than aluminum precipitation in the first melt and the liquidus temperature higher than blend melt.
In another illustrative aspect, aluminum precipitation includes aluminium-vanadium precipitating, aluminum-zirconium precipitating, aluminium-titanium precipitates, aluminium-scandium sinks It forms sediment, aluminium-cobalt precipitating, aluminium-chromium precipitating, aluminium-niobium precipitates and aluminium-tantalum precipitates and aluminium-tungsten precipitating, aluminium-molybdenum precipitating, aluminium-hafnium precipitating At least one of with aluminium-boron precipitating.
In this way, improved high temperature, wearability and/or other performances of cast aluminium alloy gold are provided.In addition, primary The formation of precipitating improve alloy from grain refining capability, to reduce or eliminate, to add external source by grain refiner brilliant The needs of grain refiner material (for example, such as titanium diboride or titanium aluminide particle).Even if mutually being tied with this Grain refiner material It closes, outer source additive, which can also be used alone, in crystal grain refinement than previously further improves.This provides improved castability and subtracts Few casting flaw.
According to the specific embodiment being provided below, other application field of the invention be will become obvious.It should manage Solution, specific embodiment and specific example are intended merely for the purpose of explanation, the range being not intended to limit the invention.
Features described above and advantage and other feature and advantage of the invention is from including claim and exemplary implementation It is in the specific embodiment of example and apparent in conjunction with attached drawing.
Detailed description of the invention
The present invention will be more fully understood according to specific embodiment and attached drawing, in which:
Fig. 1 is the schematic diagram of exemplary casting system according to the present invention;
Fig. 2 is the phasor of aluminum-zirconium;
Fig. 3 is aluminium-titanium phasor;
Fig. 4 is aluminium-silicon phasor;
Fig. 5 A is the phasor of the aluminum-zirconium alloy with a small amount of silicon as impurity;And
Fig. 5 B be with for castability about 10 silicon, and for bardenability about 1.5% copper and The phasor of the aluminum-zirconium alloy of 0.4% magnesium.
Specific embodiment
Fig. 1 is the schematic diagram of exemplary casting system 100 according to the present invention.Casting system 100 includes first chamber 102 With second chamber 104.First chamber 102 accommodates the first melt for being in the first temperature, and second chamber 104 is accommodated in the second temperature Second melt of degree.First temperature is higher than second temperature.System 100 further include in first chamber 102 and second chamber 104 The mixing chamber 106 of each connection.Mixing chamber 106 is further connected to mold 108.
In an illustrative methods, the first melt and the second melt can be introduced into mixing chamber 106 simultaneously, thus During mixing heat will the fast exchange between first and second melt, this is from causing stable aluminium in component in the first melt The fast nucleation of the dispersoid of compound precipitating.In this way, it is rapid to carry out liquid for the mixing of the second melt of low temperature and the first melt It is cold, wherein forming the precipitating of high-temperature stable in blend melt.Then blend melt comprising high temperature precipitations is flowed from mixing chamber Enter in mold, the solidification of melt is mixed in the mold.Make high temperature precipitations in from mixing chamber fast transition to mold The aggregation of (or " dispersoid ") minimizes.In addition, the low diffusion of obtained transition metal atoms minimizes in a mold Dispersoid is transformed into more complicated intermetallic phase and during any subsequent heat treatment or makes during blend melt solidifies Inhibit dissolution in the temperature course undergone with period casting.This leads to the casting for the high-temperature behavior for having stable.
In one exemplary embodiment, the first melt includes one of aluminium and peritectoid transition metal element, and Be maintained at a temperature of liquidus temperature higher than the first melt in first chamber 102, and the second melt include aluminium alloy simultaneously And lower than the first melt liquidus temperature and be higher than blend melt liquidus temperature at a temperature of be maintained at second chamber In 104.
It is the silicon of known poisonous substance that second melt, which can also include to high temperature precipitations formation reaction, but can be in the second melt It is interior to provide silicon to improve the castability of blend melt during casting.In this way, containing higher silicon components is prepared respectively Two melts.Second melt can also contain age-hardening element, for example, such as copper and magnesium.
In this way, can adjust the composition of two kinds of precursor melts, temperature and volume with optimize aluminide volume fraction and Dispersion is to provide optimum performance.The second melt of low melting point eutectic is maintained at temperature more lower than the first melt, causes first Temperature of the melt in mix stages reduces rapidly, this just be introduced into mold and it is subsequent will solidify leading clouding close it is molten The nucleation of body high temperature precipitate dispersions body.Therefore, The inventive process provides two kinds of mutually exclusive Hirschfeld-Klinger reactions, in institute It obtains and the primary transition metal aluminide of height crystal grain refinement is provided in casting.
Table 1
Table 1 shows one group of illustrative bath component and temperature, mixes and leads before introducing die cavity just Cause that there is the subject alloy for improving characteristic.First melt be maintained at a temperature of 1000 degrees Celsius in first chamber 102 and Second melt is maintained at a temperature of 600 degrees Celsius in second chamber 104.First melt contains transition metal element, for example, Such as zirconium and vanadium, usually with pass through peritectic reaction during the second melt mixed in mixing chamber 106 and solidify.Because of peritectoid The property of reaction, so may only form very small amount of dispersoid during solidification, and because of the high temperatures of the phase formed Matter, so then disperse phase cannot be formed using solid-state heat treatment process.In contrast, the second melt contains than the first melt The concentration of much higher silicon, copper and magnesium.As described above, those elements improve the castability of blend melt and provide precipitating by force The benefit of change.
Although Fig. 1 shows the mixing chamber 106 outside mold 108, mixing chamber 106 can be located at other Position, for example, the casting chamber such as, but not limited in mold.In general, blend melt should introduced casting cavity by mixing It is carried out before room, so that melt is uniform in mold, to provide consistent quality and characteristic in entire casting.Casting quality is special The inconsistent or difference of property is one of problems solved by the invention.
Referring now to Fig. 2, when the first melt of high temperature in mixing chamber 106 with the second melt mixed of lower temperature When, the first melt is quenched from complete liquid to the two-phase liquid of phase Figure 200 and disperse body region.The first melt of high temperature is initially from phase A point in figure starts.Point A corresponds to the melt of complete liquid.When the first melt and the second melt mixed, temperature is reduced, from And the first melt is caused to be quenched, as being converted to shown in B point in phase Figure 200 from A point.Once temperature, which passes through, just puts lower section at " A " Curve, some solid ZrAl3 will initially form.This Liquid-liquid quenching leads to the precipitating immediately of high-temperature-phase ZrAl3, As shown in the line at " C ".Maximize the quantity of dispersoid by the high drive generated by temperature change, to make dispersoid Size minimize.Then before being introduced into mold and start disperse before solidification through the mixing that occurs in mixing chamber 106 Body is evenly distributed in entire blend melt.
The subsequent solidification immediately of casting occurs rapidly, this eliminate dispersoid any apparent growth or its to more complicated Intermetallic phase transformation.In this way, resulting disperse phase provides the primary of the crystal grain refinement for facilitating casting The fabulous core of solidified aluminum.
Fig. 3 provides the phasor that another exemplary high temperature melt of high-temperature-phase can be formed in similar peritectic reaction 300.In traditional casting alloy, because the solubility of hydrogen increases with temperature, pouring temperature must be minimized.Compared with High hydrogen content will increase the porosity of gained solidification casting.Only for centesimal titanium is put into aluminium alloy, melt Temperature just must be over about 900 degrees Celsius, as shown in the phasor of Fig. 3.On the contrary, conventional alloys are being more than Celsius no more than about 720 It is cast at a temperature of degree.Therefore, other than those of described in the text, the invention allows to provide many other high-temperature-phases, And impossible phase before being not limited to.
The melt of higher temperature be maintained at just on melt liquidus curve at a temperature of.The composition of melt can be wrapped substantially Include aluminium and other any amount of peritectoid transition metal elements, for example, such as, but not limited to zirconium, scandium, cobalt, chromium, niobium, tantalum, titanium, Vanadium, tungsten, molybdenum etc..The total amount of all elements may be limited to gained liquidus temperature in alloy.In the exemplary embodiment, melt About 1,000 degrees Celsius of temperature be may remain in hereinafter, can still be heated to 1,200 degrees Celsius or more in a short time Height, for example, if can then be undergone using the on-demand manufacture melt of fusing system immediately, fusing system can only be melted often immediately on demand Quantity of material needed for a casting.In such a system, 1000 degrees Celsius of temperature may be exceeded only in the temperature short time.
The melt of lower temperature may remain at a temperature of the liquidus temperature of the melt or more.It can control the melt Composition so that liquidus temperature minimum form with the nearly Eutectic Silicon in Al-Si Cast Alloys for providing about 10-12% silicon, wherein blend melt is with about The silicon of 6-10% silicon forms.Alloying element in the melt of lower temperature may further include the element for improving hardenability, than It such as, such as copper and magnesium, but also may include other elements, for example, such as silver, zinc, manganese.In one exemplary embodiment, The melt of lower temperature may include the copper of about 0.5-5.5%, the magnesium of about 0.1-0.6%, the zinc of about 0.1-3.0% and/or about The hybrid alloys composition of the manganese of 0.1-0.6%.
Blend melt leads to the temperature of the liquidus temperature of blend melt composition or more.In view of high-temperature fusant and low temperature The rule of the composition of melt, mixture can determine composition, temperature and volume.After blending, can be cast immediately with Minimize the coalescence of high temperature dispersoid.It is more complicated that the low diffusion of transition metal atoms is transformed into process of setting high temperature dispersoid Intermetallic phase, and inhibit dissolution in heat treatment temperature and at use temperature, to generate stable height during the casting service life Warm nature energy.
Fig. 5 A shows the phasor 500 of the aluminum-zirconium alloy with a small amount of silicon as impurity.Fig. 5 B shows to have and be used for About 10 silicon of castability, and the aluminum-zirconium alloy of about 1.5% copper and 0.4% magnesium for bardenability Phasor 502.Compare two phasors 500 and 502 and illustrate silicon, the addition of copper and magnesium can prevent from forming high temperature at room temperature ZrAl3.The present invention avoids this problem by following: controlling the dynamics that disperse phase is formed by quenching high-temperature fusant alloy It being mutually distributed to prevent to balance, this is illustrated by phasor 500, to form dispersoids in two kinds of alloy mixing periods, then casting mixing Melt forms needed for Castability and subsequent heat treatment the remaining phase for generating precipitation-hardening to solidify blend melt.? The high temperature precipitations formed during two kinds of melt mixeds do not dissolve during subsequent solidification, because of the zirconium in these temperature ranges The diffusion rate of (and other transition metal) is very low.This explains disperse phase cannot be formed by conventional method, for example, for example Pass through heat treatment.
Fig. 4 shows aluminium-silicon phasor 400.Traditional casting alloy usually contains about 6% to 10% silicon.Therefore, liquid Liquidus temperature is about 620-640 degrees Celsius, allows to be poured under about 720 degrees Celsius (that is, 100 degrees Celsius of overheats).At one Illustrative aspect, the melt of lower temperature contain the silicon than these conventional alloys higher amounts, it means that melt has about 600 to take the photograph The even lower liquidus curve of family name's degree.By the lower temperature, high silicon melt and high-temperature-phase melt mixed will increase high silicon melt Temperature, while the silicon amount in blend melt is reduced, this makes the liquidus temperature of blend melt be higher by initial high silicon melt.This will be mixed The temperature for closing melt maintains the required overheat being higher by under about 100 degrees Celsius, and required overheat is higher by the liquidus curve of blend melt Temperature.In this way, the relatively low hold temperature of low temperature high silicon melt reduces hydrogen content, and leads to the stomata in final casting Rate is lower.
The composition of adjustable two kinds of precursor melts, temperature and volume are to optimize aluminide volume fractiion and dispersion to obtain Obtain the required performance in casting.
The following table 2 shows the exemplary range of preferably a set of melt:
Table 2
The following table 3 shows a preferred embodiment of melt:
Table 3
Table 4 shows another preferred embodiment of melt:
Table 4
Table 5 shows one group of specific exemplary fusion condition:
Table 5
The blend melt composition that table 6 to 8 shows other exemplary melt composition and obtains:
Initial melt 1 Initial melt 2 Subject alloy
Weight 20 80 100.00
Si 0.1 12 9.62
Fe 0.1 0.5 0.42
Cu 0.1 3.5 2.82
Mg 0.1 0.5 0.42
Ti 0.3 0.1 0.14
Mn 0.3 0.1 0.14
Zn 0.1 0.5 0.42
V 0.5 0.01 0.108
Zr 0.5 0.01 0.108
Temperature 1200 620 736
Table 6
Table 7
Table 8
In another exemplary embodiment again, primary silicon can be refined to improve the wear-resisting property of such as gained casting.It is existing Fig. 4 is being returned to, the melt of higher temperature may include the aluminium alloy of high silicon content.At about 900 degrees celsius, there is about 25% silicon Alloy be completely melt, as shown in the point " A " in phasor 400.The melt of lower temperature includes eutectic or hypoeutectic composition, such as Shown in point " B " in phasor 400.Combined alloy (or blend melt) is indicated by point " C ", because of the power of a large amount of just grade silicon crystals Core is studied, so being formed in traditional hypereutectic alloy or than the alloy in the range of previous higher silicon.The casting of combined alloy " C " The fine structure of silicon crystal is maintained, so that the Main Patterns of subsequent solidification are eutectic freezings, and primary crystal growth It is some.This is provides possibility using chemical modifier in the melt of lower temperature, so that cured eutectic structure is kept It is modified, realize the microstructure for showing primary silicon and modified Eutectic Silicon in Al-Si Cast Alloys unavailable so far.
In one exemplary embodiment, the present invention can produce the component for internal combustion engine, for example, such as aluminium alloy vapour Cylinder cap has improved high-temperature behavior compared with previously achievable.In this way, cylinder cover is able to bear higher temperature Degree, which improve the efficiency of combustion process, this can provide the vehicle of improved fuel economy and/or improved combination internal combustion engine Performance, the internal combustion engine has the aluminium cylinder cover of feature that is combined with and can obtain by using the present invention.
The specification is substantially merely illustrative, is in no way intended to limit the present invention, application or purposes.Of the invention Introduction can be implemented in a variety of manners extensively.Therefore, although the present invention includes particular instance, true scope of the invention is not It should so be restricted, because other modifications will be apparent after specification and following claims in research attached drawing.

Claims (9)

1. a kind of system for cast aluminium alloy gold comprising:
For accommodating the first chamber for being in the first melt of the first temperature;
For accommodating the second chamber for being in the second melt of the second temperature lower than first temperature;
It is connected to the first chamber and the second chamber molten for receiving described first from the first chamber simultaneously Body and second melt from the second chamber and the mixing chamber being mixed;And
The mold of the blend melt is connected to and is used to receive with the mixing chamber.
2. system according to claim 1, wherein first melt includes aluminium and at least one peritectoid transition metal member Element.
3. system according to claim 1, wherein first melt include zirconium, scandium, cobalt, chromium, niobium, tantalum, titanium, vanadium, tungsten, One of molybdenum, hafnium and boron.
4. system according to claim 1, wherein second melt, which has, includes percentage higher than first melt The composition of the silicon of ratio.
5. system according to claim 1, wherein second melt, which has, includes percentage higher than first melt The composition of the copper of ratio.
6. system according to claim 1, wherein second melt, which has, includes percentage higher than first melt The composition of the magnesium of ratio.
7. system according to claim 1, wherein first temperature is higher than the liquid phase of aluminum precipitation in first melt Line temperature, and the second temperature is lower than the liquidus temperature of aluminum precipitation in first melt and is higher than the blend melt Liquidus temperature.
8. system according to claim 1, wherein first temperature is higher than the liquid phase of aluminum precipitation in first melt Line temperature, and the second temperature is lower than the liquidus temperature of aluminum precipitation in first melt and is lower than the blend melt Liquidus temperature.
9. system according to claim 7, wherein the aluminum precipitation includes aluminium-vanadium precipitating, aluminum-zirconium precipitates, aluminium-titanium sinks Shallow lake, aluminium-scandium precipitating, aluminium-cobalt precipitating, aluminium-chromium precipitating, aluminium-niobium precipitates and aluminium-tantalum precipitates and aluminium-tungsten precipitating, aluminium-molybdenum are heavy At least one of shallow lake, aluminium-hafnium precipitating and aluminium-boron precipitating.
CN201810474172.0A 2017-05-31 2018-05-17 The system and method that transition metal during stablizing primary solidification in cast aluminium alloy gold precipitates Pending CN108971456A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US15/609155 2017-05-31
US15/609,155 US20180347011A1 (en) 2017-05-31 2017-05-31 System and method to stabilize transition metal precipitates in cast aluminum alloys during primary solidification

Publications (1)

Publication Number Publication Date
CN108971456A true CN108971456A (en) 2018-12-11

Family

ID=64279396

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810474172.0A Pending CN108971456A (en) 2017-05-31 2018-05-17 The system and method that transition metal during stablizing primary solidification in cast aluminium alloy gold precipitates

Country Status (3)

Country Link
US (1) US20180347011A1 (en)
CN (1) CN108971456A (en)
DE (1) DE102018113000A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111809083A (en) * 2019-04-12 2020-10-23 通用汽车环球科技运作有限责任公司 Aluminum alloy composition for simplifying semi-solid casting process and semi-solid casting method

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101018630A (en) * 2004-07-26 2007-08-15 爱尔兰都柏林国立大学-都柏林大学 A method for producing a functionally gradient component
US20080311418A1 (en) * 2007-06-18 2008-12-18 Husky Injection Molding Systems Ltd. Metal-Molding System and Process for Making Foamed Alloy
US20100297467A1 (en) * 2009-05-21 2010-11-25 Sawtell Ralph R Method of producing ingot with variable composition using planar solidification
CN106191562A (en) * 2016-08-17 2016-12-07 椤惧缓 The material of a kind of Cast aluminium alloy gold and preparation method
CN106191561A (en) * 2016-08-17 2016-12-07 椤惧缓 A kind of aluminium alloy and preparation method thereof

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101018630A (en) * 2004-07-26 2007-08-15 爱尔兰都柏林国立大学-都柏林大学 A method for producing a functionally gradient component
US20080311418A1 (en) * 2007-06-18 2008-12-18 Husky Injection Molding Systems Ltd. Metal-Molding System and Process for Making Foamed Alloy
US20100297467A1 (en) * 2009-05-21 2010-11-25 Sawtell Ralph R Method of producing ingot with variable composition using planar solidification
CN106191562A (en) * 2016-08-17 2016-12-07 椤惧缓 The material of a kind of Cast aluminium alloy gold and preparation method
CN106191561A (en) * 2016-08-17 2016-12-07 椤惧缓 A kind of aluminium alloy and preparation method thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111809083A (en) * 2019-04-12 2020-10-23 通用汽车环球科技运作有限责任公司 Aluminum alloy composition for simplifying semi-solid casting process and semi-solid casting method

Also Published As

Publication number Publication date
US20180347011A1 (en) 2018-12-06
DE102018113000A1 (en) 2018-12-06

Similar Documents

Publication Publication Date Title
Ward et al. Semi-solid processing of novel MMCs based on hypereutectic aluminium-silicon alloys
EP2396436B1 (en) Aluminium die casting alloy
US6132532A (en) Aluminum alloys and method for their production
EP2112242A1 (en) Heat treatable L12 aluminium alloys
EP2241644A1 (en) Heat treatable L12 aluminum alloys
CN108300884B (en) A kind of hypoeutectic Al-Mg2The rotten and thinning method of Si alloy
GB2553366A (en) A casting alloy
CN110016593B (en) Aluminum alloy and preparation method thereof
US11713500B2 (en) Advanced cast aluminum alloys for automotive engine application with superior high-temperature properties
Ghiaasiaan et al. Effect of alloy composition on microstructure and tensile properties of net-shaped castings of Al–Zn–Mg–Cu alloys
CN108220729A (en) A kind of high-strength temperature-resistant cast magnesium alloy and preparation method thereof
CN108971456A (en) The system and method that transition metal during stablizing primary solidification in cast aluminium alloy gold precipitates
Hashim et al. Influence of short heat treatment on the microstructures and mechanical properties of Thixoformed aluminum alloy composite
Pei et al. Forming and properties of 7075 aluminum alloy by rheological squeeze casting with transverse mobile injection feed
CN114672701B (en) High-strength multi-element eutectic casting aluminum alloy and preparation method thereof
CN104911410A (en) Aluminum alloy refiner intermediate alloy and preparation method thereof
JP4691799B2 (en) Aluminum casting alloy for piston and manufacturing method of piston
Nowak Development of Niobium Boron grain retainer for aluminium silicon alloys
CN103014391B (en) The alloy preparation method of a kind of improvement 2618 aluminium alloy micostructure
Chen et al. Microstructure Observation of Naturally Aged Thixoforming ZA27 Alloy
Wang et al. Effect of Sc on As-Cast Microstructures and Mechanical Properties of Al-Si-Mg-Cu-Ti Alloys
WO2018046368A1 (en) A casting alloy
Zhang et al. Effect of nickel alloying and mechanical stirring on the microstructure and mechanical properties of Al–10% Si–5% Cu alloy
Mahallawi et al. Understanding the Role of Nanodispersions on the Properties of A390 Hypereutectic Al-Si Cast Alloy
KR20040042469A (en) Thixocast magnesium alloy and method for manufacturing the same

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20181211

WD01 Invention patent application deemed withdrawn after publication