WO2006057452A1 - Aluminum hot forged article, and method for producing the same - Google Patents

Aluminum hot forged article, and method for producing the same Download PDF

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Publication number
WO2006057452A1
WO2006057452A1 PCT/JP2005/022142 JP2005022142W WO2006057452A1 WO 2006057452 A1 WO2006057452 A1 WO 2006057452A1 JP 2005022142 W JP2005022142 W JP 2005022142W WO 2006057452 A1 WO2006057452 A1 WO 2006057452A1
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Prior art keywords
mass
base material
recited
forged article
producing
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PCT/JP2005/022142
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French (fr)
Inventor
Yasuji Kawamata
Kazuhiro Kobori
Tomoaki Yamanoi
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Showa Denko K.K.
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Publication of WO2006057452A1 publication Critical patent/WO2006057452A1/en

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    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D5/00Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
    • C25D5/48After-treatment of electroplated surfaces
    • C25D5/50After-treatment of electroplated surfaces by heat-treatment
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/02Pretreatment of the material to be coated, e.g. for coating on selected surface areas
    • C23C2/022Pretreatment of the material to be coated, e.g. for coating on selected surface areas by heating
    • C23C2/0224Two or more thermal pretreatments
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/26After-treatment
    • C23C2/28Thermal after-treatment, e.g. treatment in oil bath
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/26After-treatment
    • C23C2/28Thermal after-treatment, e.g. treatment in oil bath
    • C23C2/29Cooling or quenching
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C4/00Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
    • C23C4/02Pretreatment of the material to be coated, e.g. for coating on selected surface areas
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C4/00Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
    • C23C4/18After-treatment
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D5/00Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
    • C25D5/34Pretreatment of metallic surfaces to be electroplated
    • C25D5/42Pretreatment of metallic surfaces to be electroplated of light metals
    • C25D5/44Aluminium

Definitions

  • Thepresent invention relates to analuminumhot forgedarticle and a method for producing the same, especially to an aluminum hot forged article excellent in corrosion resistance and corrosion fatigue strength and a method for producing the same.
  • Al-Mg-Si series alloy As an aluminumalloyforsuchsuspensionparts, Al-Mg-Si series alloy is popularly used due to its excellent strength. In order to attain the weight saving thereof, there are various proposals directed to compositions, hot forging conditions, heat treatments and surface treatments to improve the strength and the corrosion resistance.
  • Patent Document 1 Japanese Unexamined Laid-open Patent Publication No. S63-103046 discloses an aluminum alloy to which trace elements such as Ti are added to enhance the strength.
  • Patent Document 2 discloses an aluminum forged member in which alloy compositions, forging conditions, solution treatments and aging conditions are regulated to improve the mechanical characteristics .
  • Patent Document 3 discloses an Al-Mg-Si series alloy member in which compositions of a zincate film for improving processing of a zinc phosphate treatment to be executed to improve the resistance to filiform rust are regulated.
  • Patent Document 4" discloses an aluminumalloyplate in which an adhesion amount of zinc phosphate in a zinc phosphate treatment to be executed to improve the resistance to filiform rust is regulated.
  • Patent Document 5" discloses an aluminumplatewhich was subjected to Zn series plating or Fe series plating, and then heated to diffuse the aluminum into the plating.
  • Patent Documents 3 to 5 cannot attain sufficient corrosive environment strength, weather resistance, corrosion resistance of a structural member such as a suspension member.
  • the present invention has been developed in view of the above-mentioned and/or other problems in the related art.
  • the present invention can significantly improve upon existing methods and/or apparatuses.
  • someembodiments canprovide an aluminum hot forged article excellent in corrosion resistance and corrosion fatigue strength.
  • someembodiments canprovide a method of producing such aluminum hot forged article.
  • Amethodformanufacturinganaluminumforgedarticleaccording tothepresentinvention hasthestructuresasrecitedinthefollowing Items [1] to [15].
  • a method for producing an aluminum heat forged article comprising the steps of: subjecting a base material of an aluminum alloy consisting essentially of Si: 0.6 to 1.5 mass%, Mg: 0.8 to 1.5 mass%, and the balance being Al and inevitable impurities to hot forging; applying Zn to a surface of the base material at a rate of
  • An aluminum forged article according to the present invention has the structures as recited in the following Items [16] to [22]
  • An aluminum forged article having a Zn concentration layer containing Zn of 0.01 mass% or more in a surface layer portion of the article.
  • a base material excluding the Zn concentration layer is formed of an aluminum alloy consisting essentially of Si: 0.6 to 1.5 mass%, Mg: 0.8 to 1.5 mass%, Zn: less than 0.01 mass%, and the balance being Al and inevitable impurities, wherein a thickness of the Zn concentration layer is 100 to 500 ⁇ m, wherein a surface Zn concentration at a depth of 5 ⁇ m from a surface of the Zn concentration layer is 1 to 10 mass%, and a mean Zn concentration of the Zn concentration layer is 0.1 mass% or more but less than 1 mass%.
  • a Zn applied layer high in adhesiveness to the base material can be formed, and the workability is good.
  • a Zn applied layer high in adhesiveness to the base material can be formed, and the workability is good.
  • the aluminum hot forged article according to the invention as recited in the aforementioned Item [16] is excellent in corrosion resistanceandcorrosionfatigue strengthdue to the Znconcentration layer formed at the surface layer portion.
  • the aluminum hot formed article according to the invention as recited in the aforementioned Item [17] is especially excellent in strength.
  • Fig. 1 is a graph schematically showing the relationship between the depth from the surface and the Zn concentration in the Zn concentration layer. Best Mode for Carrying Out the Invention
  • Si and Mg are an element to be added to increase the strength of the alloy, respectively.
  • the Si content should fall within the range of from 0.6 to 1.5 mass%. If the Si content is less than 0.6 mass%, it is difficult to secure sufficient strength by the solution treatment and the quenching treatment, and even after the subsequent agingtreatment. To the contrary, if it exceeds 1.5mass%, itbecomes difficult to suppress grain boundary precipitation even if the cooling rate is increased sufficiently, resulting in deterioration of corrosion fatigue strength.
  • the preferable Si content is 0.8 to 1.2 mass%.
  • the Mg content should fall within the range of from 0.8 to 1.5 mass%.
  • the Mg content is less than 0.8 mass%, it is difficult to secure sufficient strength by the solution treatment and the quenching treatment, and even after the subsequentagingtreatment. Tothecontrary, ifitexceeds 1.5mass%, the quenching sensitivity deteriorates, which in turn make it difficult to secure strength increasing effect even if the cooling rate is increased sufficiently.
  • the preferable Mg content is 0.8 to 1 mass%.
  • the balance of the aluminum alloy includes Al and inevitable impurities.
  • the aluminumalloy can contain a slight amount of one or more elements which can contribute to strength enhancement of the aluminum alloy.
  • elements include Cu, Mn, Cr and Fe. Excessive amount of such elements may cause deterioration of the corrosion resistance and/or deterioration of the quenching sensitivity.
  • the Cu content is 0.1 to 0.5 mass%
  • the Mn content is 0.05 to 0.5 mass%
  • the Cr content is 0.05 to 0.5 mass%
  • the Fe content is 0.5 mass% or less.
  • the Cu content is less than 0.1 mass%, the strength enhancing effect becomes poor. To the contrary, if it exceeds 0.5 mass%, the corrosion resistance may deteriorate.
  • the crystal grain miniaturization effect becomes poor.
  • quenching sensitivity is enhanced, which in turn may cause deterioration of strength.
  • Fe content exceeds 0.5 mass%, the corrosion resistance may deteriorate.
  • Strength enhancing effects can be secured when the Fe content exceeds 0.2 mass%.
  • the amount of Zn for forming the Zn concentration layer as a sacrificial corrosion layer should fall within the range of from 1 to 50 g/m 2 . If it is less than 1 g/m 2 , a sacrificial corrosion layer cannot be formed. To the contrary, the exceeding of 50 g/m 2 causes early corrosion, resulting in insufficient long term anticorrosion effect, and also causes a cost rise.
  • the preferable Zn application amount is 4 to 20 g/m 2 .
  • a thermal spraying method or a plating method can be preferably usedbecause thesemethods canattainexcellent adhesiveness between the applied Zn and the base material and excellent in workability.
  • Theaforementionedthermalsprayingmethod is not specifically limited, and the thermal spraying can be performed with a well known means suchas athermal sprayinggun. Inordertoprevent oxidization of the sprayed layer, the thermal spraying can be performed in a non-oxidization atmosphere suchas N 2 gas atmosphere.
  • the thickness of the sprayed layer is not specifically limited so long as the Zn application amount falls within the aforementioned range. Concretely, the preferable thickness of the sprayed layer is 0.1 to 20 ⁇ m. If it is less than O.l ⁇ m, it becomes difficult to control the thickness since it is too thin. To the contrary, it exceeds 20 ⁇ m, initial corrosion occurs, which makes it difficult to attain a long term anti ⁇ orrosion effect.
  • the spraying material pure Zn or Zn-Al alloy can be used.
  • the base material is produced by hot forging at 450 ° C or above and then thermal spraying is performed when the base material is still in a high temperature status of 350 ° C or above.
  • theaforementionedplatingmethod is not specifically limited, amethodusing zinc sulfateplatingbathcanbe exemplified.
  • the plating is performed at room temperature and a current density of 1 to 10 A/dm 2 .
  • the zincate treatment can be preferably performed by immersing the article in normal zincate bath containing sodium hydrate and zinc oxide as major ingredients for several ten seconds at room temperature.
  • the aforementioned plating and zincate treatment can be preferablyperformedafterthecoolingofthehotforgedbasematerial, removing of burrs if necessary, and the surface cleaning thereof. Dirt and/or oxide films can be removed by the surface cleaning, resulting in enhanced adhesiveness of the plated film or zincate film.
  • Such surface cleaning method can be any common method. Examples of such surface cleaning include cleaning using weak alkaline detergent containing surfactant, caustic wash, and a combination thereof. Such surface cleaning can preferably be applied to the case in which Zn is thermally sprayed after cooling the base material, which can enhance the adhesiveness of the Zn sprayed layer.
  • the purposes of the solution treatment are to enhance the strength improvement by heat treatment and form a Zn concentration layer by Zn diffusion.
  • strength enhancement of the alloy and formation of the Zn concentration can be simultaneously attained by single heat treatment.
  • the Zn applied to the surface diffuses in the base material in the depth direction thereof by heating to form a Zn concentration layer with a concentration gradient along the depth direction in which the Zn concentration gradually decreases from the surface portion toward the deep portion.
  • the solution treatment should be executed at 500 to 580 ° C for 5 to 180 minutes. If the temperature is less than 500 ° C or the time is less than 5 minutes, desired strength cannot be obtained since sufficient sold solubility of M 2 Si cannot be attained. To the contrary, if it exceeds 580 ° C, partial solution occurs, causing deteriorationofmechanical characteristics. This also causes deep diffusion of Zn, resulting in an excessively thick Zn concentration layer. Such excessively thick Zn concentration layer results in deteriorationof longtermanticorrosioneffects due totheincreased corrosion depth and deterioration of strength due to the increased corrosion loss. Furthermore, if the treatment time exceeds 180 minutes, theproductivitydeteriorates.
  • the solution treatment can be preferably performed at 500 to 550 0 C for 30 to 60 minutes.
  • the cooling conditions after it is cooled to 250 0 C are not specifically limited.
  • the cooling can be preferably executed at a cooling rate of 1 ° C/second or above.
  • Such Zn concentration layer of the aluminumhot forged article according to the present invention can be formed by diffusing Zn applied to the surface of the base material in the base material by heat treatment.
  • the surface portionofthe Znconcentrationlayer has thehighest Znconcentration, and the concentration gradually decreases toward the deep portion of the Zn concentration layer.
  • the Zn concentration layer is defined as a layer covering from the surface to a portion where the Zn concentration becomes higher than that of the base material by 0.01 mass%. This depth is defined as a thickness T of the Zn concentration layer.
  • the Zn concentration at any depth in the Zn concentration layer is 0.01 mass% or above. Since the sacrificial corrosion effect becomes poor if the Zn concentration is 0.01 mass% or less, the Zn concentration layer is defined as a layer containing Zn: 0.01 mass% or more as mentioned above.
  • the base material includes Zn of 0.01 mass% or less due to diffusion of the applied Zn in addition to Si: 0.6 to 1.5 mass?, Mg: 0.8 to 1.5 mass% before the solution treatment. Since the Zn is caused by the diffusion of the Zn applied to the surface, the Zn concentration is not constant along the depth direction. The Zn concentration becomes maximum, i.e., almost near 0.01 mass%, at the vicinity of the Zn concentration layer. The concentration gradually decreases toward the deep portion.
  • the thickness T of the Zn concentration layer should falls within the range of from 100 to 500 ⁇ m to secure a long-term anticorrosion effect. If the thickness T is less than 100 ⁇ m, corrosion exceeding the sacrificial corrosion layer occurs. Thus, a sacrificial anticorrosion effect cannot be expected. On the other hand, if it exceeds 500 ⁇ m, the final corrosion depth becomes excessively deep, whichmay cause insufficient strength as amember.
  • the preferable thickness T of the Zn concentration layer is 100 to 250 ⁇ m.
  • the Znconcentrationinthe Znconcentrationlayer is regulated by the surface Zn concentration Cs at the depth of 5 ⁇ m from the surfaceandthemeanZnconcentrationCmoftheentireZnconcentration layer. Using these two concentrations, the Zn diffusion state is regulated to secure prescribed corrosion resistance.
  • Theaforementionedmean ZnconcentrationCm is avalueobtained bydividingtheentire Znamount of anycross-section in the thickness direction of the articlewith the thickness T of the Zn concentration layer. If the mean Zn concentration Cm is less than 0.1 mass%, corrosion exceeding the sacrificial corrosion layer (Zn concentration layer) occurs. Thus, a sacrificial anticorrosion effect cannot be expected. On the other hand, if it exceeds 1 mass%, the potential of the surface of the Zn concentration layer becomes unnecessary low, which enhances excessive corrosion. Thus, a long-term anticorrosion effect cannot be obtained.
  • the preferable mean Zn concentration Cm is 0.1 to 0.5 mass%.
  • the aluminumhot forged article according to the present invention is excellent incorrosionresistance andfatigue corrosion strength, it can be preferably used as various structural members/parts. Especially, sincesuchmemberhas light-weightiness of the aluminumalloy, it canbepreferablyusedas structuralmembers for vehicles. Among structural members for vehicles, it can be preferably used as a wheel related member, especially a suspension arm, which is exposed to corrosion environment and required to have both the corrosion resistance and the fatigue corrosion strength.
  • An aluminum alloy having the composition as disclosed in each Example and Comparative Example in Tables 1 to 5 was continuously forged to produce a round bar with a diameter of 15 cm (6 inches) .
  • the round bar was formed into a flat plate with a thickness of 20 mm by hot forging at 470 0 C.
  • the balance of the aluminum alloy is Al and inevitable impurities.
  • theplate Afterthehotforging, theplatewas cooledtoroomtemperature. Subsequently, the plate was subjected to caustic washing, and then subjected to zinc plating. The plating was executed at the current density of 3 A/dm 2 in plating bath of room temperature containing zinc metal, boric acid, and ammonium sulfate. The Zn application amount is shown in Tables 1 and 2.
  • the plate After hot casting, the plate was cooled to room temperature. Subsequently, the plate was subjected to caustic washing. Thereafter, the plate was immersed in zincate treatment bath of room temperature for 60 seconds, and then subjected to zinc plating under the same conditions as the aforementioned (b) .
  • the total Zn application amount by the zincate treatment and plating is shown in Tables 1 and 2.
  • each of the aluminum hot forged articles of Examples and Comparative Examples 1 to 11, 21 to 31 to which Zn was applied before solution treatment assuming that the portion in which the Zn concentration was larger than the Zn concentration of the base material by 0.01 mass% was defined as a Zn concentration layer.
  • the thickness T of this Zn concentration layer was measured.
  • the surface Zn concentration Cs at the depth of 5 ⁇ m from the surface of the Zn concentration layer and the mean Zn concentration Cm of the Zn concentration layer were measured.
  • the mean Zn concentration Cm denotes a value obtained by dividing the entire Zn amount at any cross-section in the thickness direction bythe thickness T of the Znconcentrationlayer.
  • the aforementioned each Zn concentration and the depth of the Zn concentration layer were measured by EPMA.
  • an aluminum hot forged article excellent in corrosion resistance and fatigue corrosion strength can be produced and utilized to manufacture structural members for vehicles such as suspension arms.
  • the term "preferably” is non-exclusive andmeans “preferably, but not limited to.”
  • means-plus-function or step-plus-function limitations will only be employed where for a specificclaimlimitationallof thefollowingconditions arepresent in that limitation: a) "means for” or “stepfor” is expresslyrecited; b) a corresponding function is expressly recited; and ⁇ ) structure, material or acts that support that structure are not recited.
  • the terminology "present invention” or “invention” may be used as a reference to one or more aspect within the present disclosure.

Abstract

In some embodiments, a method for producing an aluminum heat forged article excellent in corrosion resistance and corrosion fatigue strength includes the steps of: subjecting a base material of an aluminum alloy consisting essentially of Si: 0.6 to 1.5 mass%, Mg: 0.8 to 1.5 mass %, and the balance being Al and inevitable impurities to hot forging; applying Zn to a surface of the base material at a rate of 2 to 50 g/m2, subjecting the base material to solution treatment at 500 to 580 °C for 5 to 180 minutes; and subjecting the base material to quenching treatment for cooling the base material at a cooling rate of 10 ° C/second until it reaches 250 °C.

Description

DESCRIPTION
ALUMINUM HOT FORGED ARTICLE, AND METHOD FOR PRODUCING THE SAME
This application claims priority to Japanese Patent
Application No. 2004-339854 filed on November 25, 2004 and U.S.
Provisional Application S.N. 60/631,868 filed on December 1, 2004, the entire disclosures ofwhich are incorporatedherein byreference in their entireties.
Cross Reference to Related Applications
This application is an application filed under 35 U.S.C. §111(a) claiming the benefit pursuant to 35 U.S.C. §119(e)(l) of the filing date of U.S. Provisional Application S.N. 60/631,868 filed on December 1, 2004, pursuant to 35 U.S.C. §lll(b).
Technical Field
Thepresent inventionrelates to analuminumhot forgedarticle and a method for producing the same, especially to an aluminum hot forged article excellent in corrosion resistance and corrosion fatigue strength and a method for producing the same. Background Art
The following description sets forth the inventor's knowledge of related art and problems therein and should not be construed as an admission of knowledge in the prior art.
In automotive parts, recently, it is strongly required to attainweight reduction of vehicle body structural parts to increase mileage and prevent an increase of vehicle body weight. For this reason, using an aluminum as materials has rapidly become popular. Especially, in suspension parts, adoption of aluminum forged parts or aluminum extruded parts has been increased.
As an aluminumalloyforsuchsuspensionparts, Al-Mg-Si series alloy is popularly used due to its excellent strength. In order to attain the weight saving thereof, there are various proposals directed to compositions, hot forging conditions, heat treatments and surface treatments to improve the strength and the corrosion resistance.
Japanese Unexamined Laid-open Patent Publication No. S63-103046 (hereinafter, "Patent Document 1" ) discloses an aluminum alloy to which trace elements such as Ti are added to enhance the strength.
Japanese Laid-open Patent Publication No. 2002-348630 (hereinafter, "Patent Document 2") discloses an aluminum forged member in which alloy compositions, forging conditions, solution treatments and aging conditions are regulated to improve the mechanical characteristics .
Japanese Laid-open Patent Publication No. 2000-119785 (hereinafter, "Patent Document 3") discloses an Al-Mg-Si series alloy member in which compositions of a zincate film for improving processing of a zinc phosphate treatment to be executed to improve the resistance to filiform rust are regulated.
Japanese Laid-open Patent Publication No. 2000-313932 (hereinafter, "Patent Document 4" ) discloses an aluminumalloyplate in which an adhesion amount of zinc phosphate in a zinc phosphate treatment to be executed to improve the resistance to filiform rust is regulated.
Japanese Laid-open Patent Publication No. H5-78888 (hereinafter, "Patent Document 5" ) discloses an aluminumplatewhich was subjected to Zn series plating or Fe series plating, and then heated to diffuse the aluminum into the plating.
In general, it is said that 6000 series alloy (Al-Mg-Si series alloy) is excellent in corrosion resistance as compared with 7000 series alloyor 2000 series alloy. If 6000 series alloyis orientated to high strength, problems including, e.g., deterioration of ductility due to intergranular cracking or intergranular corrosion in corrosive environment arise. Especially, in parts required to havemechanicalstrength, fatiguestrengthandcorrosionresistance, deterioration of characteristics becomes a big problem. However, the composition restriction and/or the heat treatment as disclosed by Patent Documents 1 and 2 cannot sufficiently cope with the aforementioned deterioration of characteristics.
Furthermore, the surface treatments as disclosed by Patent Documents 3 to 5 cannot attain sufficient corrosive environment strength, weather resistance, corrosion resistance of a structural member such as a suspension member.
The description herein of advantages and disadvantages of various features, embodiments, methods, and apparatus disclosed in other publications is in no way intended to limit the present invention. Indeed, certain features of the inventionmaybe capable of overcoming certain disadvantages, while still retaining some orall ofthefeatures, embodiments, methods, andapparatus disclosed therein.
Other objects and advantages of the present invention will be apparent from the following preferred embodiments. Disclosure of Invention
The present invention has been developed in view of the above-mentioned and/or other problems in the related art. The present invention can significantly improve upon existing methods and/or apparatuses.
Amongotherpotentialadvantages, someembodiments canprovide an aluminum hot forged article excellent in corrosion resistance and corrosion fatigue strength.
Amongotherpotentialadvantages, someembodimentscanprovide a method of producing such aluminum hot forged article.
Amethodformanufacturinganaluminumforgedarticleaccording tothepresentinventionhasthestructuresasrecitedinthefollowing Items [1] to [15].
[I] A method for producing an aluminum heat forged article, comprising the steps of: subjecting a base material of an aluminum alloy consisting essentially of Si: 0.6 to 1.5 mass%, Mg: 0.8 to 1.5 mass%, and the balance being Al and inevitable impurities to hot forging; applying Zn to a surface of the base material at a rate of
2 to 50 g/m2; subjecting the base material to solution treatment at 500 to 580 0C for 5 to 180 minutes; and subjectingthebasematerialtoquenchingtreatmentforcooling the base material at a cooling rate of 10 ° C/second or more until it reaches 250 0C.
[2] The method for producing an aluminum heat forged article as recited in the aforementioned Item 1, wherein the aluminum alloy further includes one or more elements selected from the group consisting of Cu: 0.1 to 0.5 mass%, Mn: 0.05 to 0.5 mass%, Cr: 0.05 to 0.5 mass%, and Fe: 0.5 mass% or less.
[3] The method for producing an aluminum heat forged article as recited in the aforementioned Item ϊ, wherein the application of Zn is executed by thermal spraying.
[4] The method for producing an aluminum heat forged article as recited in the aforementioned Item 2, wherein the application of Zn is executed by thermal spraying.
[5] The method for producing an aluminum heat forged article as recitedin the aforementionedItem3, wherein the thermal spraying of Zn is executed when the hot forged base material is in a hot-temperature state of 350 ° C or above without cooling the base material. [6] The method for producing an aluminum heat forged article as recitedin the aforementioned Item 4, wherein the thermal spraying of Zn is executed when the hot forged base material is in a hot-temperature state of 3500C or above without cooling the base material.
[7] The method for producing an aluminumheat forged article as recited in the aforementioned Item 1, wherein the application of Zn is executed by plating.
[8] Themethod forproducing an aluminumheat forged article as recited in the aforementioned Item 2, wherein the application of Zn is executed by plating.
[9] The method for producing an aluminum heat forged article as recited in the aforementioned Item 7, wherein zincate treatment is executed as pretreatment of the plating.
[10] Themethod for producing an aluminumheat forgedarticle as recited in the aforementioned Item 8, wherein zincate treatment is executed as pretreatment of the plating.
[11] Themethod forproducing an aluminumheat forged article as recited in the aforementioned Item 1, wherein the application of Zn is executed after cooling the hot forged base material and cleaning a surface of the base material. [12] Themethod for producing an aluminumheat forged article as recited in the aforementioned Item 2, wherein the application of Zn is executed after cooling the hot forged base material and cleaning a surface of the base material.
[13] Themethodfor producing an aluminumheat forgedarticle as recited in the aforementioned Item 7, wherein the application of Zn is executed after cooling the hot forged base material and cleaning a surface of the base material.
[14] Themethodforproducing an aluminumheat forged article as recited in the aforementioned Item 8, wherein the application of Zn is executed after cooling the hot forged base material and cleaning a surface of the base material.
[15] Themethodfor producing an aluminumheat forgedarticle as recited in any one of the aforementioned Items 1 to 14, wherein the application amount of Zn is 4 to 20 g/m2.
An aluminum forged article according to the present invention has the structures as recited in the following Items [16] to [22]
[16] An aluminum forged article having a Zn concentration layer containing Zn of 0.01 mass% or more in a surface layer portion of the article. wherein a base material excluding the Zn concentration layer is formed of an aluminum alloy consisting essentially of Si: 0.6 to 1.5 mass%, Mg: 0.8 to 1.5 mass%, Zn: less than 0.01 mass%, and the balance being Al and inevitable impurities, wherein a thickness of the Zn concentration layer is 100 to 500 μm, wherein a surface Zn concentration at a depth of 5 μm from a surface of the Zn concentration layer is 1 to 10 mass%, and a mean Zn concentration of the Zn concentration layer is 0.1 mass% or more but less than 1 mass%.
[17] The aluminum forged article as recited in the aforementioned Item 16, wherein the aluminum alloy further includes one or more elements selected from the group consisting of Cu: 0.1 to 0.5 mass%, Mn: 0.05 to 0.5 mass%, Cr: 0.05 to 0.5 mass%, and Fe: 0.5 mass% or less.
[18] The aluminum forged article as recited in the aforementioned Item 16, wherein the aluminum hot forged article is a structural member for vehicles.
[19] The aluminum forged article as recited in the aforementioned Item 17, wherein the aluminum hot forged article is a structural member for vehicles.
[20] The aluminum forged article as recited in the aforementioned Item 18, wherein the aluminum hot forged article is a wheel related member.
[21] The aluminum forged article as recited in the aforementioned Item 19, wherein the aluminum hot forged article is a wheel related member.
[22] The aluminum forged article as recited in the aforementioned Item 20 or 21, wherein the wheel related member is a suspension arm.
Effects of the Invention
According to the method for producing the aluminum hot forged article of the present invention [1] , since a Zn concentration layer can be formed at the surface of the base material due to the heating at the time of the solution treatment, an aluminumhot forged article excellent in corrosion resistance and corrosion fatigue strength can be produced.
According to the invention as recited in the aforementioned Item [2], the strength of the aluminum hot forged article can be enhanced.
According to the invention as recited in the aforementioned Items [3] and [4], a Zn applied layer high in adhesiveness to the base material can be formed, and the workability is good.
According to the invention as recited in the aforementioned Items [5] and [6] , analuminumhotforgedarticleespeciallyexcellent in adhesiveness between the base material and the applied Zn layer can be produced.
According to the invention as recited in the aforementioned Items [7] and [8], a Zn applied layer high in adhesiveness to the base material can be formed, and the workability is good.
According to the invention as recited in each of the aforementioned Items [9] to [14], an aluminum hot forged article especially excellent in adhesiveness between the base material and the applied Zn layer can be produced.
According to the invention as recited in the aforementioned Item [15], a Zn concentration layer excellent especially in long term anticorrosion effect can be formed.
The aluminum hot forged article according to the invention as recited in the aforementioned Item [16] is excellent in corrosion resistanceandcorrosionfatigue strengthdue to the Znconcentration layer formed at the surface layer portion.
The aluminum hot formed article according to the invention as recited in the aforementioned Item [17] is especially excellent in strength.
According to the invention as recited in the aforementioned Item [18] and [19], a structural member for vehicles excellent in corrosionresistanceandcorrosion fatigue strengthcanbeprovided.
According to the invention as recited in the aforementioned Item [20] and [21], a wheel related member excellent in corrosion resistance and corrosion fatigue strength can be provided.
According to the invention as recited in the aforementioned Item [22], a suspension arm excellent in corrosion resistance and corrosion fatigue strength can be provided.
Brief Description of Drawings
The preferred embodiments of the present invention are shown by way of example, and not limitation, in the accompanying figures, in which:
Fig. 1 is a graph schematically showing the relationship between the depth from the surface and the Zn concentration in the Zn concentration layer. Best Mode for Carrying Out the Invention
In the following paragraphs, some preferred embodiments of the inventionwill be describedbyway of example andnot limitation. It should be understood based on this disclosure that various other modifications can be made by those in the art based on these illustrated embodiments.
In a method for producing an aluminum hot forged article according to the present invention, aluminum alloy compositions ofabasematerialare specified, andsolutiontreatment andquenching treatment are executed after the application of Zn to the surface of the base material to thereby secure strength. Further, a Zn concentration layer as a sacrificial corrosion layer is formed at the surface layer portion.
In the aluminum alloy compositions of the base material, Si and Mg are an element to be added to increase the strength of the alloy, respectively. The Si content should fall within the range of from 0.6 to 1.5 mass%. If the Si content is less than 0.6 mass%, it is difficult to secure sufficient strength by the solution treatment and the quenching treatment, and even after the subsequent agingtreatment. To the contrary, if it exceeds 1.5mass%, itbecomes difficult to suppress grain boundary precipitation even if the cooling rate is increased sufficiently, resulting in deterioration of corrosion fatigue strength. The preferable Si content is 0.8 to 1.2 mass%. On the other hand, the Mg content should fall within the range of from 0.8 to 1.5 mass%. If the Mg content is less than 0.8 mass%, it is difficult to secure sufficient strength by the solution treatment and the quenching treatment, and even after the subsequentagingtreatment. Tothecontrary, ifitexceeds 1.5mass%, the quenching sensitivity deteriorates, which in turn make it difficult to secure strength increasing effect even if the cooling rate is increased sufficiently. The preferable Mg content is 0.8 to 1 mass%. The balance of the aluminum alloy includes Al and inevitable impurities.
In addition to the aforementioned Si andMg, the aluminumalloy can contain a slight amount of one or more elements which can contribute to strength enhancement of the aluminum alloy. Examples of such element include Cu, Mn, Cr and Fe. Excessive amount of such elements may cause deterioration of the corrosion resistance and/or deterioration of the quenching sensitivity. Accordingly, it is preferable that the Cu content is 0.1 to 0.5 mass%, the Mn content is 0.05 to 0.5 mass%, the Cr content is 0.05 to 0.5 mass%, and the Fe content is 0.5 mass% or less. In detail, if the Cu content is less than 0.1 mass%, the strength enhancing effect becomes poor. To the contrary, if it exceeds 0.5 mass%, the corrosion resistance may deteriorate. If the Mn content and Cr content are less than 0.05 mass% respectively, the crystal grain miniaturization effect becomes poor. To the contrary, if each of them exceeds 0.5 mass%, quenching sensitivity is enhanced, which in turn may cause deterioration of strength. Furthermore, if Fe content exceeds 0.5 mass%, the corrosion resistance may deteriorate. Strength enhancing effects can be secured when the Fe content exceeds 0.2 mass%. By adding one or any combination of the aforementioned elements, strength enhancing effects can be attained.
The amount of Zn for forming the Zn concentration layer as a sacrificial corrosion layer should fall within the range of from 1 to 50 g/m2. If it is less than 1 g/m2, a sacrificial corrosion layer cannot be formed. To the contrary, the exceeding of 50 g/m2 causes early corrosion, resulting in insufficient long term anticorrosion effect, and also causes a cost rise. The preferable Zn application amount is 4 to 20 g/m2.
AlthoughtheZnapplicationmethodisnotspecificallylimited, a thermal spraying method or a plating method can be preferably usedbecause thesemethods canattainexcellent adhesiveness between the applied Zn and the base material and excellent in workability.
Theaforementionedthermalsprayingmethodisnot specifically limited, and the thermal spraying can be performed with a well known means suchas athermal sprayinggun. Inordertoprevent oxidization of the sprayed layer, the thermal spraying can be performed in a non-oxidization atmosphere suchas N2gas atmosphere. The thickness of the sprayed layer is not specifically limited so long as the Zn application amount falls within the aforementioned range. Concretely, the preferable thickness of the sprayed layer is 0.1 to 20 μm. If it is less than O.lμm, it becomes difficult to control the thickness since it is too thin. To the contrary, it exceeds 20 μm, initial corrosion occurs, which makes it difficult to attain a long term antiσorrosion effect. As the spraying material, pure Zn or Zn-Al alloy can be used. In order to enhance the adhesiveness between the base material and the thermally sprayed layer, it is preferable that the base material is produced by hot forging at 450 ° C or above and then thermal spraying is performed when the base material is still in a high temperature status of 350 ° C or above.
Althoughtheaforementionedplatingmethodisnot specifically limited, amethodusing zinc sulfateplatingbathcanbe exemplified. As to the conditions of theplating, it is preferable that the plating is performed at room temperature and a current density of 1 to 10 A/dm2. In order to enhance the adhesiveness of the plated layer, it is also preferable to perform zincate treatment as pretreatment of the plating. The zincate treatment can be preferably performed by immersing the article in normal zincate bath containing sodium hydrate and zinc oxide as major ingredients for several ten seconds at room temperature.
The aforementioned plating and zincate treatment can be preferablyperformedafterthecoolingofthehotforgedbasematerial, removing of burrs if necessary, and the surface cleaning thereof. Dirt and/or oxide films can be removed by the surface cleaning, resulting in enhanced adhesiveness of the plated film or zincate film. Such surface cleaning method can be any common method. Examples of such surface cleaning include cleaning using weak alkaline detergent containing surfactant, caustic wash, and a combination thereof. Such surface cleaning can preferably be applied to the case in which Zn is thermally sprayed after cooling the base material, which can enhance the adhesiveness of the Zn sprayed layer.
The purposes of the solution treatment are to enhance the strength improvement by heat treatment and form a Zn concentration layer by Zn diffusion. By applying Zn before executing the solution treatment, strength enhancement of the alloy and formation of the Zn concentration can be simultaneously attained by single heat treatment. The Zn applied to the surface diffuses in the base material in the depth direction thereof by heating to form a Zn concentration layer with a concentration gradient along the depth direction in which the Zn concentration gradually decreases from the surface portion toward the deep portion.
The solution treatment should be executed at 500 to 580 ° C for 5 to 180 minutes. If the temperature is less than 500 ° C or the time is less than 5 minutes, desired strength cannot be obtained since sufficient sold solubility of M2Si cannot be attained. To the contrary, if it exceeds 580 ° C, partial solution occurs, causing deteriorationofmechanical characteristics. This also causes deep diffusion of Zn, resulting in an excessively thick Zn concentration layer. Such excessively thick Zn concentration layer results in deteriorationof longtermanticorrosioneffects due totheincreased corrosion depth and deterioration of strength due to the increased corrosion loss. Furthermore, if the treatment time exceeds 180 minutes, theproductivitydeteriorates. The solution treatment can be preferably performed at 500 to 550 0C for 30 to 60 minutes.
In the quenching treatment to be executed after the solution treatment, inorderto securepredeterminedstrength, it isnecessary to quickly cool the base material at a cooling rate of 10 ° C/second or more until it reaches 250 0C. In other words, if the cooling is performed at a cooling rate of 10 ° C/second or more until it reaches 250 0C, predetermined strength can be obtained. If the cooling rate is less than 10 ° C/second, sufficient strength cannot be obtained since M2Si solution will separate out. The preferable cooling rate is 50 ° C/second or above. Although the cooling method is not specifically limited, water cooling and two-phase cooling of water cooling + compressed air cooling can be exemplified.
Furthermore, the cooling conditions after it is cooled to 250 0C are not specifically limited. For example, the cooling can be preferably executed at a cooling rate of 1 ° C/second or above.
After the quenching treatment, aging treatment can be arbitrarily performed to further enhance the strength. Such aging treatment can be preferably performed at 150 to 200 ° C for 2 to 48 hours. If it is less than 1500C, it takes a significantly long time to reach the highest strength, which is not preferable in terms oftheproductionefficiency. Ontheotherhand, ifitexceeds 200° C, the time range for obtaining the highest strength becomes short, which makes it difficult to perform the production management. It is more preferable that the aging treatment is executed at 160 to 190 0C for 5 to 24 hours.
An aluminum hot forged article according to the present invention has a prescribed Zn concentration layer at a surface of a base material, and can be produced by, for example, the aforementioned method of the present invention.
Such Zn concentration layer of the aluminumhot forged article according to the present invention can be formed by diffusing Zn applied to the surface of the base material in the base material by heat treatment. In this case, as shown in Fig. 1, the surface portionofthe Znconcentrationlayerhas thehighest Znconcentration, and the concentration gradually decreases toward the deep portion of the Zn concentration layer. In this invention, the Zn concentration layer is defined as a layer covering from the surface to a portion where the Zn concentration becomes higher than that of the base material by 0.01 mass%. This depth is defined as a thickness T of the Zn concentration layer. In other words, the Zn concentration at any depth in the Zn concentration layer is 0.01 mass% or above. Since the sacrificial corrosion effect becomes poor if the Zn concentration is 0.01 mass% or less, the Zn concentration layer is defined as a layer containing Zn: 0.01 mass% or more as mentioned above.
The base material includes Zn of 0.01 mass% or less due to diffusion of the applied Zn in addition to Si: 0.6 to 1.5 mass?, Mg: 0.8 to 1.5 mass% before the solution treatment. Since the Zn is caused by the diffusion of the Zn applied to the surface, the Zn concentration is not constant along the depth direction. The Zn concentration becomes maximum, i.e., almost near 0.01 mass%, at the vicinity of the Zn concentration layer. The concentration gradually decreases toward the deep portion.
The thickness T of the Zn concentration layer should falls within the range of from 100 to 500 μm to secure a long-term anticorrosion effect. If the thickness T is less than 100 μm, corrosion exceeding the sacrificial corrosion layer occurs. Thus, a sacrificial anticorrosion effect cannot be expected. On the other hand, if it exceeds 500 μm, the final corrosion depth becomes excessively deep, whichmay cause insufficient strength as amember. The preferable thickness T of the Zn concentration layer is 100 to 250 μm.
The Znconcentrationinthe Znconcentrationlayeris regulated by the surface Zn concentration Cs at the depth of 5 μm from the surfaceandthemeanZnconcentrationCmoftheentireZnconcentration layer. Using these two concentrations, the Zn diffusion state is regulated to secure prescribed corrosion resistance.
The surface Zn concentration Cs should fall within the range of from 1 to 10 mass%. If the surface Zn concentration Cs is less than 1 mass%, corrosion exceeding the sacrificial corrosion layer occurs. Thus, a sacrificial anticorrosion effect cannot be expected. On the other hand, if it exceeds 10 mass%, the potential of the surface of the aluminum hot forged article becomes unnecessary low, which enhances excessive corrosion. Thus, a long-term anticorrosion effect cannot be obtained. The preferable surface Zn concentration Cs is 5 to 10 mass%.
Theaforementionedmean ZnconcentrationCmis avalueobtained bydividingtheentire Znamount of anycross-section in the thickness direction of the articlewith the thickness T of the Zn concentration layer. If the mean Zn concentration Cm is less than 0.1 mass%, corrosion exceeding the sacrificial corrosion layer (Zn concentration layer) occurs. Thus, a sacrificial anticorrosion effect cannot be expected. On the other hand, if it exceeds 1 mass%, the potential of the surface of the Zn concentration layer becomes unnecessary low, which enhances excessive corrosion. Thus, a long-term anticorrosion effect cannot be obtained. The preferable mean Zn concentration Cm is 0.1 to 0.5 mass%. Since the aluminumhot forged article according to the present inventionis excellent incorrosionresistance andfatigue corrosion strength, it can be preferably used as various structural members/parts. Especially, sincesuchmemberhas light-weightiness of the aluminumalloy, it canbepreferablyusedas structuralmembers for vehicles. Among structural members for vehicles, it can be preferably used as a wheel related member, especially a suspension arm, which is exposed to corrosion environment and required to have both the corrosion resistance and the fatigue corrosion strength.
EXAMPLES
[Production of aluminum hot forged article]
An aluminum alloy having the composition as disclosed in each Example and Comparative Example in Tables 1 to 5 was continuously forged to produce a round bar with a diameter of 15 cm (6 inches) . The round bar was formed into a flat plate with a thickness of 20 mm by hot forging at 470 0C. In each Table, the balance of the aluminum alloy is Al and inevitable impurities.
Next, Zn was applied to each surface of the flat plates except forComparativeExamples 12 and32byanyoneof the followingmethods.
(a) Thermal spraying
Subsequent to the hot thermal forging, pure Zn was thermally sprayed to a plate which was in a hot temperature statue of 350 ° C without being cooled through a thermal spraying gun disposed one side of the plate. The thermal spraying conditions were: thermal spraying voltage: 30 V, thermal spraying currency: 50 A, thermal spraying distance: 200 mm, and Zn application amount: shown inTables 1-5.
(b) Plating
Afterthehotforging, theplatewas cooledtoroomtemperature. Subsequently, the plate was subjected to caustic washing, and then subjected to zinc plating. The plating was executed at the current density of 3 A/dm2 in plating bath of room temperature containing zinc metal, boric acid, and ammonium sulfate. The Zn application amount is shown in Tables 1 and 2.
(c) Zincate treatment + Plating
After hot casting, the plate was cooled to room temperature. Subsequently, the plate was subjected to caustic washing. Thereafter, the plate was immersed in zincate treatment bath of room temperature for 60 seconds, and then subjected to zinc plating under the same conditions as the aforementioned (b) . The total Zn application amount by the zincate treatment and plating is shown in Tables 1 and 2.
Next, each plate to which Zn was applied was subjected to solution treatment at temperature for a certain time as shown in Tables 1 to 5. Immediately thereafter, quenching treatment was executed. The quenching was performed so that the plate was cooled to 250 ° C by water cooling or two-phase cooling (water + compressed air) atthecoolingrateasshowninTables 1to5. Afterthequenching, the plate was further subjected to aging treatment of 180 0C x 8 hours. Thus, an aluminum hot forged article was obtained.
In the aluminum hot forged article, Zn applied to the surface of the plate by solution treatment was diffused in the basematerial, and a layer containing Zn in its base material at high density was formed at a surface layer portion of the plate. In the Zn diffusion layer, the surface portion had the highest Zn concentration, and the Zn concentration gradually decreased toward the deep portion.
On the other hand, as to the plates of Comparative Examples 12 and 32, without applying Zn, each plate was subjected only to solution treatment, quenching treatment and aging treatment to obtain an aluminum hot forged article.
[Zn concentration layer in aluminum hot forged article]
As to each of the aluminum hot forged articles of Examples and Comparative Examples 1 to 11, 21 to 31 to which Zn was applied before solution treatment, assuming that the portion in which the Zn concentration was larger than the Zn concentration of the base material by 0.01 mass% was defined as a Zn concentration layer. the thickness T of this Zn concentration layer was measured. Furthermore, the surface Zn concentration Cs at the depth of 5 μm from the surface of the Zn concentration layer and the mean Zn concentration Cm of the Zn concentration layer were measured. The mean Zn concentration Cm denotes a value obtained by dividing the entire Zn amount at any cross-section in the thickness direction bythe thickness T of the Znconcentrationlayer. The aforementioned each Zn concentration and the depth of the Zn concentration layer were measured by EPMA.
The thickness T of the Zn concentration, surface Zn concentration Cs and mean Zn concentration Cm are also shown in Tables 1 to 5.
[Mechanical characteristics of aluminum hot forged article]
The tensile strengthandelongationof eachplateweremeasured by a well known method. These results are also in Tables 1 to 5.
[Corrosion resistance of aluminum hot forged article]
In SWAAT (Synthetic sea Water Acetic Acid salt spray Test) , using corrosion test liquid of ASTM D1141, a cycle of spraying the corrosion test liquid for 0.5 hour and then holding for 1.5 hours was repeated for 320 hours. After the SWAAT, corrosion depth was measured, and it was evaluated as one of the following four levels depending on the corrosion state. These results are also shown in Tables 1 to 5.
©: Corrosiondepthwas shallow, andgeneralcorrosionoccurred
O: general corrosion occurred, but the corrosion depth was
•shallower than the thickness of the Zn concentration layer
Δ: Intergranular corrosion or pitting corrosion occurred,
and the corrosion depth was less than 250 μm
X : Intergranular corrosion or pitting corrosion occurred,
and the corrosion depth was 250 μm or more
[Fatigue corrosion strength of aluminum hot forged article]
After the corrosion test in accordancewith SWAAT, aflat plate test piece with a Zn concentratin layer (corroded surface in Comparative Example 14) only remained on one side was cut out, and subjected to a plate bending fatigue test. The test conditions were minimal maximal stress ratio R=-l, stress value: 200 MPa, number of cycles: 105 times. The decreasing rate of the fatigue strength with respect to 6061-T6 material (no corrosion) as a comparison materialwasobtained. Basedonthedecreasingrate, itwasevaluated as the followingthree levels. The evaluationresults are also shown in Tables 1 to 5.
O: Decreasing rate was less than 20%
Δ: Decreasing rate was more than 20% but less than 40%
X : Decreasing rate was more than 40% c 2r
-4
Figure imgf000028_0001
Figure imgf000029_0001
K)
K>
90
Figure imgf000029_0002
S1 cr
CD U)
K)
Figure imgf000030_0001
cr
CO
O
Figure imgf000031_0001
CX fϋ
Figure imgf000032_0001
As will be understood from the results shown in Tables 1 to 5, it was confirmed that the aluminum hot forged articles produced by the method of Examples were excellent in corrosion resistance and fatigue corrosion strength.
Industrial Applicability
According to the present invention, an aluminum hot forged article excellent in corrosion resistance and fatigue corrosion strength can be produced and utilized to manufacture structural members for vehicles such as suspension arms.
While the present invention may be embodied in many different forms, a number of illustrative embodiments are described herein withtheunderstandingthat thepresentdisclosureis tobeconsidered as providing examples of the principles of the invention and such examples are not intended to limit the invention to preferred embodiments described herein and/or illustrated herein.
While illustrative embodiments of the invention have been describedherein, the present invention is not limitedto thevarious preferred embodiments described herein, but includes any and all embodiments having equivalent elements, modifications, omissions, combinations (e.g., of aspects across various embodiments), adaptations and/or alterations as would be appreciated by those in the art based on the present disclosure. The limitations in the claims are to be interpreted broadly based on the language employed in the claims and not limited to examples described in the present specification or during the prosecution of the application, which examples are to be construed as non-exclusive. For example, in the present disclosure, the term "preferably" is non-exclusive andmeans "preferably, but not limited to." In this disclosure and during the prosecution of this application, means-plus-function or step-plus-function limitations will only be employed where for a specificclaimlimitationallof thefollowingconditions arepresent in that limitation: a) "means for" or "stepfor" is expresslyrecited; b) a corresponding function is expressly recited; and σ) structure, material or acts that support that structure are not recited. In this disclosure and during the prosecution of this application, the terminology "present invention" or "invention" may be used as a reference to one or more aspect within the present disclosure. The language present invention or invention should not be improperly interpreted as an identification of criticality, should not be improperlyinterpretedas applyingacross all aspects orembodiments (i.e., it should be understood that the present invention has a number of aspects and embodiments), and should not be improperly interpreted as limiting the scope of the application or claims. In this disclosure and during the prosecution of this application, the terminology "embodiment" can be used to describe any aspect, feature, process orstep, anycombinationthereof, and/oranyportion thereof, etc. In some examples, various embodiments may include overlappingfeatures . Inthis disclosure andduringtheprosecution of this case, the following abbreviated terminologymaybe employed: "e.g. " which means "for example; " and "NB" which means "note well. "

Claims

1. A method for producing an aluminum heat forged article, comprising the steps of: subjecting a base material of an aluminum alloy consisting essentially of Si: 0.6 to 1.5 mass%, Mg: 0.8 to 1.5 mass%, and the balance being Al and inevitable impurities to hot forging; applying Zn to a surface of the base material at a rate of 2 to 50 g/m2; subjecting the base material to solution treatment at 500 to 580 0C for 5 to 180 minutes; and subjectingthebasematerialtoquenchingtreatmentforcooling the base material at a cooling rate of 10 ° C/second or more until it reaches 250 ° C.
2. The method for producing an aluminum heat forged article as recited in claim 1, wherein the aluminum alloy further includes one or more elements selected from the group consisting of Cu: 0.1 to 0.5 mass%, Mn: 0.05 to 0.5 mass%, Cr: 0.05 to 0.5 mass%, and Fe: 0.5 mass% or less.
3. The method for producing an aluminum heat forged article as recited in claim 1, wherein the application of Zn is executed by thermal spraying.
4. The method for producing an aluminum heat forged article as recited in claim 2, wherein the application of Zn is executed by thermal spraying.
5. The method for producing an aluminum heat forged article as recited in claim 3, wherein the thermal spraying of Zn is executed when the hot forged base material is in a hot-temperature state of 350 0C or above without cooling the base material.
6. The method for producing an aluminum heat forged article as recited in claim 4, wherein the thermal spraying of Zn is executed when the hot forged base material is in a hot-temperature state of 350 ° C or above without cooling the base material.
7. The method for producing an aluminum heat forged article as recited in claim 1, wherein the application of Zn is executed by plating.
8. The method for producing an aluminum heat forged article as recited in claim 2, wherein the application of Zn is executed by plating.
9. The method for producing an aluminum heat forged article as recited in claim 7, wherein zincate treatment is executed as pretreatment of the plating.
10. The method for producing an aluminum heat forged article as recited in claim 8, wherein zincate treatment is executed as pretreatment of the plating.
11. The method for producing an aluminum heat forged article as recited in claim 1, wherein the application of Zn is executed after cooling the hot forged base material and cleaning a surface of the base material.
12. The method for producing an aluminum heat forged article as recited in claim 2, wherein the application of Zn is executed after cooling the hot forged base material and cleaning a surface of the base material.
13. The method for producing an aluminum heat forged article as recited in claim 7, wherein the application of Zn is executed after cooling the hot forged base material and cleaning a surface of the base material.
14. The method for producing an aluminum heat forged article as recited in claim 8, wherein the application of Zn is executed after cooling the hot forged base material and cleaning a surface of the base material.
15. The method for producing an aluminum heat forged article as recited in any one of claims 1 to 14, wherein the application amount of Zn is 4 to 20 g/m2.
16. AnaluminumforgedarticlehavingaZnconcentrationlayer containing Zn of 0.01 mass% or more in a surface layer portion of the article, wherein a base material excluding the Zn concentration layer is formed of an aluminum alloy consisting essentially of Si: 0.6 to 1.5 mass%, Mg: 0.8 to 1.5 mass%, Zn: less than 0.01 mass%, and the balance being Al and inevitable impurities, wherein a thickness of the Zn concentration layer is 100 to 500 μm, wherein a surface Zn concentration at a depth of 5 μm from a surface of the Zn concentration layer is 1 to 10 mass%, and a mean Zn concentration of the Zn concentration layer is 0.1 mass% or more but less than 1 mass%.
17. Thealuminumforgedarticleasrecitedinclaim16, wherein the aluminum alloy further includes one or more elements selected from the group consisting of Cu: 0.1 to 0.5 mass%, Mn: 0.05 to 0.5 mass%, Cr: 0.05 to 0.5 mass%, and Fe: 0.5 mass% or less.
18. Thealuminumforgedarticleasrecitedinclaim16, wherein the aluminumhot forged article is a structural member for vehicles.
19. Thealuminumforgedarticleasrecitedinclaim17, wherein the aluminumhot forged article is a structural member for vehicles.
20. Thealuminumforgedarticleasrecitedinclaim18, wherein the aluminum hot forged article is a wheel related member.
21. Thealuminumforgedarticleasrecitedinclaim19, wherein the aluminum hot forged article is a wheel related member.
22. The aluminum forged article as recited in claim 20 or 21, wherein the wheel related member is a suspension arm.
PCT/JP2005/022142 2004-11-25 2005-11-25 Aluminum hot forged article, and method for producing the same WO2006057452A1 (en)

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Publication number Priority date Publication date Assignee Title
CN102844456A (en) * 2010-04-16 2012-12-26 昭和电工株式会社 Process for production of forged aluminum alloy member

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JPS63186857A (en) * 1987-01-27 1988-08-02 Showa Alum Corp Manufacture of pressed product made of corrosion-resisting aluminum alloy
JPS6447896A (en) * 1987-08-17 1989-02-22 Showa Aluminum Corp Surface treatment of heat exchanger made of aluminum
JPH05331627A (en) * 1992-06-03 1993-12-14 Nippon Steel Corp Surface reforming method for aluminum plate
JPH07157861A (en) * 1993-12-07 1995-06-20 Kobe Steel Ltd Aluminum extruded shape material for piping excellent in corrosion resistance
JP2002060881A (en) * 2000-08-22 2002-02-28 Nippon Light Metal Co Ltd Aluminum alloy for casting and forging, and method for producing casting and forging material
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JPS63186857A (en) * 1987-01-27 1988-08-02 Showa Alum Corp Manufacture of pressed product made of corrosion-resisting aluminum alloy
JPS6447896A (en) * 1987-08-17 1989-02-22 Showa Aluminum Corp Surface treatment of heat exchanger made of aluminum
JPH05331627A (en) * 1992-06-03 1993-12-14 Nippon Steel Corp Surface reforming method for aluminum plate
JPH07157861A (en) * 1993-12-07 1995-06-20 Kobe Steel Ltd Aluminum extruded shape material for piping excellent in corrosion resistance
JP2002060881A (en) * 2000-08-22 2002-02-28 Nippon Light Metal Co Ltd Aluminum alloy for casting and forging, and method for producing casting and forging material
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CN102844456A (en) * 2010-04-16 2012-12-26 昭和电工株式会社 Process for production of forged aluminum alloy member

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