JP2869889B2 - Thixocasting method - Google Patents
Thixocasting methodInfo
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- JP2869889B2 JP2869889B2 JP7308175A JP30817595A JP2869889B2 JP 2869889 B2 JP2869889 B2 JP 2869889B2 JP 7308175 A JP7308175 A JP 7308175A JP 30817595 A JP30817595 A JP 30817595A JP 2869889 B2 JP2869889 B2 JP 2869889B2
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Description
【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION
【0001】[0001]
【発明の属する技術分野】本発明はチクソキャスティン
グ法、特に、亜共晶組成を有し、且つ示差熱分析曲線に
おいて、共晶溶解による第1山形吸熱部と、共晶点より
も高融点の成分の溶解による第2山形吸熱部とが存在す
る合金材料に加熱処理を施して、固相(略固体となって
いる相、以下同じ)と液相とが共存する半溶融合金材料
を調製し、次いで、加圧下で、半溶融合金材料の鋳型キ
ャビティへの充填と、それに次ぐ半溶融合金材料の凝固
とを行う方法の改良に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a thixocasting method, and more particularly, to a method having a hypoeutectic composition and a differential thermal analysis curve, wherein a first chevron-shaped heat-absorbing part due to eutectic melting has a melting point higher than the eutectic point. A semi-molten alloy material in which a solid phase (substantially solid phase, the same applies hereinafter) and a liquid phase coexist is prepared by subjecting the alloy material having the second chevron heat-absorbing part due to the dissolution of the components to heat treatment. It then relates to an improved method for filling the mold cavity with semi-solid alloy material under pressure and subsequently solidifying the semi-solid alloy material.
【0002】[0002]
【従来の技術】従来、この種チクソキャスティング法に
おいては、第1山形吸熱部の下降終了点の温度をT2 と
し、また第2山形吸熱部のピークの温度をT3 としたと
き、半溶融合金材料の鋳造温度TをT2 ≦T≦T3 に設
定している。2. Description of the Related Art Conventionally, in this type of thixocasting method, when the temperature at the descent end point of the first chevron heat absorbing portion is T 2 and the peak temperature of the second chevron heat absorbing portion is T 3 , semi-melting occurs. The casting temperature T of the alloy material is set to T 2 ≦ T ≦ T 3 .
【0003】このように鋳造温度Tを比較的高く設定す
る理由は、半溶融合金材料の固相率を低めてその鋳造性
を良好にするためである。The reason why the casting temperature T is set to be relatively high is to lower the solid phase ratio of the semi-molten alloy material to improve its castability.
【0004】この場合、得られた合金鋳物の金属組織
は、固相の凝固によるα相と、マトリックス、したがっ
て液相の凝固によるα−β共晶相とからなり、合金鋳物
はその金属組織に応じた機械的特性を有する。In this case, the metal structure of the obtained alloy casting is composed of an α phase formed by solidification of a solid phase and an α-β eutectic phase formed by solidification of a matrix and, therefore, a liquid phase. Has appropriate mechanical properties.
【0005】[0005]
【発明が解決しようとする課題】前記のような合金鋳物
の機械的特性をさらに向上させるためには、そのマトリ
ックスにβ相を微細に晶出させることが考えられるが、
従来法によったのでは、β相の微細晶出は実現不可能で
ある。In order to further improve the mechanical properties of the alloy casting as described above, it is conceivable to finely crystallize the β phase in the matrix.
According to the conventional method, fine crystallization of the β phase cannot be realized.
【0006】[0006]
【課題を解決するための手段】本発明は、亜共晶組成を
有する合金材料を用いてβ相の微細晶出を実現し得る前
記チクソキャスティング法を提供することを目的とす
る。SUMMARY OF THE INVENTION An object of the present invention is to provide a thixocasting method capable of realizing fine crystallization of a β phase using an alloy material having a hypoeutectic composition.
【0007】前記目的を達成するため本発明によれば、
亜共晶組成を有し、且つ示差熱分析曲線において、共晶
溶解による第1山形吸熱部と、共晶点よりも高融点の成
分の溶解による第2山形吸熱部とが存在する合金材料に
加熱処理を施して、固相と液相とが共存する半溶融合金
材料を調製し、次いで、加圧下で、前記半溶融合金材料
の鋳型キャビティへの充填と、それに次ぐ前記半溶融合
金材料の凝固とを行うチクソキャスティング法におい
て、前記第1山形吸熱部の上昇開始点の温度をT1 と
し、またその下降終了点の温度をT2 としたとき、前記
半溶融合金材料の鋳造温度TをT1 ≦T≦T2 に設定す
るチクソキャスティング法が提供される。[0007] To achieve the above object, according to the present invention,
In an alloy material having a hypoeutectic composition and having, in a differential thermal analysis curve, a first chevron-shaped heat absorbing portion due to eutectic melting and a second chevron-shaped heat absorbing portion due to dissolution of a component having a higher melting point than the eutectic point. A heat treatment is performed to prepare a semi-solid alloy material in which a solid phase and a liquid phase coexist, and then, under pressure, filling the mold cavity with the semi-solid alloy material, and then the semi-solid alloy material In the thixocasting method of performing solidification, when the temperature at the rising start point of the first chevron heat absorbing portion is T 1 and the temperature at the falling end point is T 2 , the casting temperature T of the semi-molten alloy material is A thixocasting method is provided wherein T 1 ≦ T ≦ T 2 .
【0008】鋳造温度Tを前記のように設定すると、そ
の温度Tの範囲、即ち、T1 ≦T≦T2 では液相は共晶
組成を有する。そして、凝固過程においては、その液相
の組成が共晶点を境にして過共晶側および亜共晶側へ揺
らぐように変化するので、過共晶側ではβ相が晶出し、
また亜共晶側ではα−β共晶相が晶出する。When the casting temperature T is set as described above, the liquid phase has a eutectic composition in the range of the temperature T, ie, T 1 ≦ T ≦ T 2 . Then, in the solidification process, the composition of the liquid phase changes so as to fluctuate from the eutectic point to the hypereutectic side and the hypoeutectic side, so that the β phase is crystallized on the hypereutectic side,
On the hypoeutectic side, an α-β eutectic phase is crystallized.
【0009】この場合、β相の成長は、固相であるα相
により妨げられるので、その微細化が達成される。In this case, since the growth of the β phase is hindered by the α phase, which is a solid phase, miniaturization is achieved.
【0010】また鋳造温度Tを前記のように設定する
と、半溶融合金材料の固相率が高くなるが、β相が固相
相互の凝集を阻止する作用を発揮するので、半溶融合金
材料は良好な流動性を有する。When the casting temperature T is set as described above, the solid phase ratio of the semi-molten alloy material is increased, but since the β phase exerts an action of inhibiting solid phase mutual aggregation, the semi-molten alloy material is Has good fluidity.
【0011】これにより、鋳造欠陥の発生が無く、また
機械的特性を従来のものよりも向上させた亜共晶組成の
合金鋳物を得ることができる。As a result, it is possible to obtain an alloy casting having a hypoeutectic composition with no occurrence of casting defects and improved mechanical properties as compared with the conventional one.
【0012】ただし、鋳造温度TがT<T1 では合金材
料において液相を存在させることができず、一方、T>
T2 では従来法のごとくβ相の晶出を実現することがで
きない。[0012] However, the casting temperature T is T <can not be present liquid phase at T 1 in the alloy material, whereas, T>
In T 2 can not achieve crystallization of the β-phase as the conventional method.
【0013】[0013]
表1は、亜共晶組成を有するAl−Si系合金材料の化
学成分を示す。このAl−Si系合金材料は、連続鋳造
法の適用下で鋳造された高品質な長尺連続鋳造材より切
出されたものであって、その鋳造に当ってはα−Alの
球状化処理が行われている。Al−Si系合金材料の寸
法は直径50mm、長さ65mmである。Table 1 shows the chemical components of the Al-Si alloy material having a hypoeutectic composition. This Al-Si alloy material is cut out from a high-quality long continuous casting material cast under the application of a continuous casting method, and in the casting, α- Al spheroidizing treatment is performed. Has been done. The dimensions of the Al-Si alloy material are 50 mm in diameter and 65 mm in length.
【0014】[0014]
【表1】 [Table 1]
【0015】Al−Si系合金材料について示差走査熱
量測定(DSC)を行ったところ、図2の結果を得た。
図2の示差熱分析曲線aにおいて、共晶溶解による第1
山形吸熱部bと、共晶点よりも高融点の成分の溶解によ
る第2山形吸熱部cとが存在する。第1山形吸熱部bの
上昇開始点dの温度T1 はT1 =556℃、下降終了点
(第2山形吸熱部cの上昇開始点、以下同じ)eの温度
T2 はT2 =580℃、第2山形吸熱部cのピークfの
温度T3 はT3 =598℃である。また第1山形吸熱部
bのピークgの温度は571℃、第2山形吸熱部cの下
降終了点hの温度は608℃である。Differential scanning calorimetry (DSC) was performed on the Al-Si alloy material, and the result shown in FIG. 2 was obtained.
In the differential thermal analysis curve a of FIG.
There is a chevron heat absorbing portion b and a second chevron heat absorbing portion c due to dissolution of a component having a higher melting point than the eutectic point. Temperature T 1 of the rising start point d in the first angled endothermic section b is T 1 = 556 ° C., lowering the end point (rising start point of the second angled endothermic section c, hereinafter the same) is the temperature T 2 of the e T 2 = 580 ° C and the temperature T 3 at the peak f of the second chevron heat absorbing portion c is T 3 = 598 ° C. The temperature at the peak g of the first chevron heat absorbing portion b is 571 ° C., and the temperature at the descent end point h of the second chevron heat absorbing portion c is 608 ° C.
【0016】次に、Al−Si系合金材料を誘導加熱装
置の加熱コイル内に設置し、次いで周波数 1kHz、
最大出力 37kWの条件で加熱して、固相と液相とが
共存する半溶融Al−Si系合金材料を調製した。この
場合、半溶融Al−Si系合金材料の加熱温度は575
℃、またその固相率は70%に設定された。Next, the Al—Si alloy material is placed in the heating coil of the induction heating device, and then the frequency is set to 1 kHz.
Heating was performed under the condition of a maximum output of 37 kW to prepare a semi-solid Al-Si alloy material in which a solid phase and a liquid phase coexist. In this case, the heating temperature of the semi-solid Al-Si alloy material is 575
° C and its solid fraction was set to 70%.
【0017】その後、図1に示すように、半溶融Al−
Si系合金材料5をチャンバ6に設置し、半溶融Al−
Si系合金材料5の鋳造温度T=575℃(T1 ≦T≦
T2)、加圧プランジャ9の移動速度 0.2m/sec
、金型温度 250℃の条件で半溶融Al−Si系合
金材料5を加圧しつつゲート7を通過させてキャビティ
4内に充填した。そして、加圧プランジャ9をストロー
ク終端に保持することによってキャビティ4内に充填さ
れた半溶融Al−Si系合金材料5に加圧力を付与し、
その加圧下で半溶融Al−Si系合金材料5を凝固させ
てAl合金鋳物A1 を得た。Thereafter, as shown in FIG.
The Si-based alloy material 5 is placed in the chamber 6 and the semi-solid Al-
Casting temperature T of Si-based alloy material 5 = 575 ° C. (T 1 ≦ T ≦
T 2 ), moving speed of the pressure plunger 9 0.2 m / sec
The semi-molten Al-Si alloy material 5 was passed through the gate 7 and pressurized under the condition of a mold temperature of 250 ° C. to fill the cavity 4. Then, by applying pressure to the semi-molten Al-Si alloy material 5 filled in the cavity 4 by holding the pressure plunger 9 at the end of the stroke,
Its under pressure solidifying the semi-molten Al-Si based alloy material 5 was obtained Al alloy casting A 1.
【0018】比較のため、半溶融Al−Si系合金材料
5の鋳造温度TをT=585℃(T2 ≦T≦T3 )に、
また固相率を45%にそれぞれ設定した、ということ以
外は前記と同一条件で前記同様の鋳造作業を行ってAl
合金鋳物A2 を得た。For comparison, the casting temperature T of the semi-solid Al—Si alloy material 5 was set to T = 585 ° C. (T 2 ≦ T ≦ T 3 ).
The same casting operation was performed under the same conditions as above, except that the solid phase ratio was set to 45%.
To obtain an alloy castings A 2.
【0019】図3,4(a)はAl合金鋳物A1 の金属
組織を示す顕微鏡写真、図4(b)は図4(a)の要部
写図である。この金属組織は、固相の凝固によるα−A
l相と、マトリックスM、したがって液相の凝固による
初晶Si相およびAl−Si共晶相とからなる。この場
合、初晶Si相は固相周りに分散し、その体積分率Vf
はVf=2.8%であった。The main part of FIG 3, 4 (a) micrograph showing the metallographic Al alloy castings A 1 is FIG. 4 (b) FIGS. 4 (a)
It is a map . This metal structure is formed by solidification of α-A
1 phase and a matrix M, thus a primary Si phase and an Al-Si eutectic phase due to solidification of the liquid phase. In this case, the primary crystal Si phase is dispersed around the solid phase, and its volume fraction Vf
Was Vf = 2.8%.
【0020】このように亜共晶組成を有するAl−Si
系合金材料を用いたのにも拘らず、前記のような、初晶
Si相が存する金属組織が得られる理由は次の通りであ
る。即ち、鋳造温度TをT=575℃に設定すると、そ
の温度Tが、図2においてT1 (556℃)≦T(57
5℃)≦T2 (580℃)の範囲に属することから液相
は図5に示すように11.7重量%Siの共晶組成を有
する。そして、凝固過程においては、その液相の組成が
図5、曲線iで示すように共晶点を境にして過共晶側お
よび亜共晶側へ揺らぐように変化するので、過共晶側で
は初晶Si相が晶出し、また亜共晶側ではAl−Si共
晶相が晶出する。Al-Si having a hypoeutectic composition
Despite the use of the base alloy material, the reason why the metal structure in which the primary crystal Si phase exists can be obtained as described above is as follows. That is, when the casting temperature T is set to T = 575 ° C., the temperature T becomes T 1 (556 ° C.) ≦ T (57
The liquid phase has a eutectic composition of 11.7% by weight of Si as shown in FIG. 5 because it belongs to the range of 5 ° C. ≦ T 2 (580 ° C.). In the solidification process, the composition of the liquid phase changes so as to fluctuate from the eutectic point to the hypereutectic side and the hypoeutectic side as shown by the curve i in FIG. , A primary Si phase is crystallized, and an Al-Si eutectic phase is crystallized on the hypoeutectic side.
【0021】この場合、初晶Si相の成長は、固相であ
るα−Al相により妨げられるので、その粒径Dは5μ
m≦D≦20μmとなる。過共晶組成を有するAl−S
i系合金材料を用いて重力鋳造を行うに際し、P等を使
用して初晶Si相の微細化が行われているが、この場合
には初晶Si相の粒径Dは20μm≦D≦50μmであ
り、これと比較すると、前記方法によれば初晶Si相の
一層の微細化が達成されていることが判る。In this case, the growth of the primary Si phase is hindered by the solid phase α-Al phase, so that the particle diameter D is 5 μm.
m ≦ D ≦ 20 μm. Al-S having hypereutectic composition
In performing gravity casting using an i-based alloy material, the primary crystal Si phase is refined using P or the like. In this case, the particle diameter D of the primary crystal Si phase is 20 μm ≦ D ≦ In comparison with this, it can be seen that according to the method, further refinement of the primary Si phase was achieved.
【0022】また鋳造温度Tを前記のように設定する
と、半溶融Al−Si系合金材料の固相率が70%とい
ったように高くなるが、初晶Si相が固相相互の凝集を
阻止する作用を発揮するので、半溶融Al−Si系合金
材料は良好な流動性を有し、Al合金鋳物A1 において
鋳造欠陥の発生は認められなかった。When the casting temperature T is set as described above, the solid fraction of the semi-molten Al-Si alloy material becomes as high as 70%, but the primary Si phase prevents the solid phase from agglomerating. since cause an effect, the semi-molten Al-Si based alloy material has good flow properties, occurrence of casting defects in the Al alloy castings a 1 was observed.
【0023】図6,7(a)はAl合金鋳物A2 の金属
組織を示す顕微鏡写真、図7(b)は図7(a)の要部
写図である。この金属組織は固相の凝固によるα−Al
相と、マトリックスM、したがって液相の凝固によるA
l−Si共晶相とからなり、初晶Si相は存在しない。The main part of FIG 6, 7 (a) micrograph, FIG. 7 showing a metallographic Al alloy castings A 2 is (b) the FIGS. 7 (a)
It is a map . The metal structure is α-Al by solidification of the solid phase.
Phase and matrix A and thus A by solidification of the liquid phase
It is composed of an l-Si eutectic phase and has no primary Si phase.
【0024】このように初晶Si相が不存在である理由
は次の通りである。即ち、鋳造温度TをT=585℃に
設定すると、その温度Tが、図2においてT2 (580
℃)≦T(585℃)≦T3 (598℃)の範囲に属す
ることから液相は図5に示すように約10.4重量%S
iの亜共晶組成を有する。そして、凝固過程において
は、その組成が図5、曲線jで示すように約10.4重
量%Siを境にして高Si側および低Si側へ揺らぐよ
うに変化するが、共晶点を超えることはなく、したがっ
て初晶Si相は晶出しない。The reason why the primary crystal Si phase is not present is as follows. That is, when the casting temperature T is set to T = 585 ° C., the temperature T becomes T 2 (580) in FIG.
C) ≦ T (585 ° C.) ≦ T 3 (598 ° C.), the liquid phase is about 10.4% by weight S as shown in FIG.
i having a hypoeutectic composition. In the solidification process, as shown by the curve j in FIG. 5, the composition changes so as to fluctuate toward the high Si side and the low Si side at about 10.4 wt% Si, but exceeds the eutectic point. Therefore, the primary Si phase does not crystallize.
【0025】次に、両Al合金鋳物A1 ,A2 よりそれ
ぞれテストピースA1 ,A2 を作製し、それらA1 ,A
2 にT6処理を施した後引張り試験およびシャルピー衝
撃試験を行ったところ、表2の結果を得た。Next, to produce both Al alloy castings A 1, respectively from A 2 Test piece A 1, A 2, which A 1, A
2 was subjected to a T6 treatment, and then subjected to a tensile test and a Charpy impact test. The results shown in Table 2 were obtained.
【0026】[0026]
【表2】 [Table 2]
【0027】表2から明らかなように、初晶Si相が存
在するテストピースA1 は、初晶Si相の無いテストピ
ースA2 に比べて強度が向上している。またテストピー
スA1 においては、初晶Si相の微細化が図られると共
にその体積分率Vfが適当であることから、延性および
靱性の低下が抑制されている。 〔実施例2〕表3は亜共晶組成を有するAl−Si系合
金材料B1 〜B3 および過共晶組成を有するAl−Si
系合金材料B4 の化学成分を示す。これらAl−Si系
合金材料B1 等は、連続鋳造法の適用下で鋳造された高
品質な長尺連続鋳造材より切出されたものであって、そ
の鋳造に当ってはα−Alの球状化処理が行われてい
る。Al−Si系合金材料B1 等の寸法は直径50mm、
長さ65mmである。As is clear from Table 2, the test piece A 1 having the primary crystal Si phase has improved strength as compared with the test piece A 2 having no primary crystal Si phase. In the test piece A 1, since the volume fraction Vf with fine primary crystal Si phase is achieved is appropriate, reduction in ductility and toughness is suppressed. Example 2 Table 3 Al-Si with Al-Si based alloy material B 1 .about.B 3 and hypereutectic composition having a hypoeutectic composition
The chemical components of the system alloy material B 4. These Al-Si alloy materials B 1 and the like are cut out from a high-quality long continuous cast material cast under the application of a continuous casting method. A spheroidizing process has been performed. Al-Si based alloy material B 1 dimensions, such as diameter 50 mm,
The length is 65 mm.
【0028】[0028]
【表3】 [Table 3]
【0029】Al−Si系合金材料B1 等について示差
走査熱量測定(DSC)を行ったところ、それら示差熱
分析曲線において、共晶溶解による第1山形吸熱部と、
共晶点より高融点の成分の溶解による第2山形吸熱部と
が存在することが判明した。When differential scanning calorimetry (DSC) was performed on the Al—Si alloy material B 1 and the like, the differential thermal analysis curves showed that the first peak-shaped heat absorbing portion due to eutectic melting,
It was found that there was a second chevron endothermic part due to dissolution of components having a higher melting point than the eutectic point.
【0030】表4は、それら示差熱分析曲線における各
点の温度をまとめたものである。Table 4 summarizes the temperatures at each point in the differential thermal analysis curves.
【0031】[0031]
【表4】 [Table 4]
【0032】次に、Al−Si合金材料B1 を誘導加熱
装置の加熱コイル内に設置し、次いで周波数 1kH
z、最大出力 37kWの条件で加熱して、固相と液相
とが共存する半溶融Al−Si系合金材料B1 を調製し
た。Next, the Al—Si alloy material B 1 is placed in a heating coil of an induction heating device, and then a frequency of 1 kHz is applied.
z, and heated under the conditions of maximum output 37kW, and the solid phase and the liquid phase was prepared semi-molten Al-Si based alloy material B 1 coexisting.
【0033】その後、図1に示すように、半溶融Al−
Si系合金材料B1 (符号5)をチャンバ6に設置し、
加圧プランジャ9の移動速度 0.2m/sec 、金型温
度250℃の条件で半溶融Al−Si系合金材料B1 を
加圧しつつゲート7を通過させてキャビティ4内に充填
した。そして、加圧プランジャ9をストローク終端に保
持することによってキャビティ4内に充填された半溶融
Al−Si系合金材料B1 に加圧力を付与し、その加圧
下で半溶融Al−Si系合金材料B1 を凝固させてAl
合金鋳物B1 を得た。また他のAl−Si系合金材料B
2 〜B4 を用い、前記同様の鋳造作業を行ってAl合金
鋳物B2 〜B4 を得た。Thereafter, as shown in FIG.
Si-based alloy material B 1 (symbol 5) is placed in chamber 6,
Moving speed 0.2 m / sec of the pressurizing plunger 9, in the conditions of a mold temperature of 250 ° C. and passed through a gate 7 while pressing the semi-molten Al-Si based alloy material B 1 was filled in the cavity 4. Then, the pressure was applied to the semi-molten Al-Si based alloy material B 1 filled in the cavity 4 by retaining the pressing plunger 9 in the stroke end, the semi-molten Al-Si based alloy material at that pressure Coagulate B 1 to Al
To obtain an alloy castings B 1. Another Al-Si alloy material B
With 2 .about.B 4, to obtain an Al alloy castings B 2 .about.B 4 performs the same casting operation.
【0034】各Al合金鋳物B1 〜B4 についてその金
属組織を調べたところ、その金属組織は、実施例1のA
l合金鋳物A1 と同様に、固相の凝固によるα−Al相
と、マトリックスM、したがって液相の凝固による初晶
Si相およびAl−Si共晶相とからなることが判明し
た。また各Al合金鋳物B1 〜B4 において鋳造欠陥の
発生は認められなかった。When the metal structure of each of the Al alloy castings B 1 to B 4 was examined, the metal structure was found to be A in Example 1.
Similar to l alloy casting A 1, and alpha-Al phase by solidification of the solid phase was found to consist of a matrix M, thus a primary crystal Si phase and the Al-Si eutectic phase by solidification of a liquid phase. No casting defect was found in each of the Al alloy castings B 1 to B 4 .
【0035】次に各Al−Si系合金材料B1 〜B4 に
ついて流動性試験を行った。この試験用可動金型31 と
しては、図8に示すようにそのキャビティ41 が、ゲー
ト7に連通する円形部4aと、その円形部4aから延出
して略凹字状をなす屈曲部4bとからなるものが用いら
れた。Next, a fluidity test was performed on each of the Al—Si alloy materials B 1 to B 4 . As the test movable die 3 1, its cavity 4 1 As shown in FIG. 8, a circular portion 4a which communicates with the gate 7, the bent portion 4b having a substantially concave shape extending from the circular part 4a Was used.
【0036】流動性試験に当っては、先ず、前記鋳造作
業と同様の条件にて半溶融Al−Si系合金材料B1 を
調製し、その材料B1 を前記と同様の条件でキャビティ
41に注入し、凝固させた。In the fluidity test, first, a semi-solid Al—Si alloy material B 1 is prepared under the same conditions as in the casting operation, and the material B 1 is subjected to the cavity 4 1 under the same conditions as described above. And coagulated.
【0037】型開き後、キャビティ41 の屈曲部4bに
存する凝固材料B1 の重量を測定して、その重量をAl
−Si系合金材料B1 の流動長とした。[0037] Mold Opening later by measuring the weight of the clot material B 1 existing in the bent portion 4b of the cavity 4 1, the weight of Al
It was flow length -Si alloy material B 1.
【0038】また他のAl−Si系合金材料B2 〜B4
について前記同様の流動性試験を行い、それらの流動長
を測定した。Further, other Al-Si alloy materials B 2 to B 4
Were subjected to the same fluidity test as described above, and their flow lengths were measured.
【0039】そして、Al−Si系合金材料B1 の流動
長を「1.0」として、他のAl−Si系合金材料B2
〜B4 の流動長比を求めた。The flow length of the Al—Si alloy material B 1 is set to “1.0”, and the other Al—Si alloy material B 2
It was determined flow length ratio of .about.B 4.
【0040】さらに4種のAl合金鋳物B1 〜B4 より
それぞれテストピースを作製し、それらにT6処理を施
した後シャルピー衝撃試験を行った。Further, test pieces were prepared from the four types of Al alloy castings B 1 to B 4 , respectively, subjected to T6 treatment, and then subjected to a Charpy impact test.
【0041】表5は、Al合金鋳物B1 〜B4 に関する
鋳造温度T、固相率および各種測定値を示す。Table 5 shows the casting temperature T, the solid fraction, and various measured values for the Al alloy castings B 1 to B 4 .
【0042】[0042]
【表5】 [Table 5]
【0043】表5から、各Al合金鋳物B1 〜B4 につ
いて、その鋳造温度TはT1 ≦T≦T2 に設定されたこ
とが判る。また初晶Si相の体積分率Vfが増加する
と、半溶融Al−Si系合金材料の流動性が向上すると
が判る。From Table 5, it can be seen that the casting temperature T of each of the Al alloy castings B 1 to B 4 was set to T 1 ≦ T ≦ T 2 . Also, it can be seen that as the volume fraction Vf of the primary Si phase increases, the fluidity of the semi-molten Al-Si alloy material improves.
【0044】図9は、表5に基づきAl合金鋳物B1 〜
B4 において、初晶Si相の体積分率Vfと、流動長比
およびシャルピー衝撃値との関係をグラフ化したもので
ある。FIG. 9 shows the results of the Al alloy castings B 1 to B 1 based on Table 5.
In B 4, and the volume fraction Vf of the primary crystal Si phase is a graph showing the relationship between the flow length ratio and the Charpy impact value.
【0045】表5、図9から明らかなように、Al合金
鋳物B1 〜B3 のごとく、初晶Si相の粒径Dが5μm
≦D≦20μmであって、その体積分率Vfが1.5%
≦Vf≦4.7%であれば、半溶融Al−Si系合金材
料の流動性を良好にして、鋳造欠陥の発生を防止し、ま
たAl合金鋳物の強度および靱性を確保することができ
る。As is clear from Table 5 and FIG. 9, as in the case of the Al alloy castings B 1 to B 3 , the primary crystal Si phase had a particle diameter D of 5 μm.
≦ D ≦ 20 μm and the volume fraction Vf is 1.5%
If ≦ Vf ≦ 4.7%, it is possible to improve the fluidity of the semi-molten Al—Si alloy material, prevent the occurrence of casting defects, and secure the strength and toughness of the Al alloy casting.
【0046】因に、実施例1のAl合金鋳物A1 に関す
る流動長比は1.1であった。[0046] In this connection, flow length ratio for the Al alloy castings A 1 of Example 1 was 1.1.
【0047】なお、本発明における合金材料にはAl−
Si系合金材料だけでなく、Al−CuAl2 系合金材
料、Al−Mg2 Si系合金材料、Al−AlFeSi
金属間化合物系合金材料等も含まれる。The alloy material used in the present invention is Al-
Not only Si based alloy material, Al-CuAl 2 alloy material, Al-Mg 2 Si based alloy material, Al-AlFeSi
Intermetallic compound alloy materials are also included.
【0048】[0048]
【発明の効果】本発明によれば、前記のように特定され
た手段を採用することによって、亜共晶組成を有する合
金材料を用いてβ相の微細晶出を実現させた高強度な合
金鋳物を得ることができる。According to the present invention, a high-strength alloy which realizes fine crystallization of β phase using an alloy material having a hypoeutectic composition by employing the means specified as described above. Castings can be obtained.
【図1】加圧鋳造機の縦断正面図である。FIG. 1 is a vertical sectional front view of a pressure casting machine.
【図2】Al−Si系合金の示差熱分析曲線である。FIG. 2 is a differential thermal analysis curve of an Al—Si alloy.
【図3】Al合金鋳物の一例の金属組織を示す顕微鏡写
真である。FIG. 3 is a micrograph showing a metal structure of an example of an Al alloy casting.
【図4】(a)は図3の部分拡大写真に相当し、(b)
は(a)の要部写図である。4A is a partially enlarged photograph of FIG. 3, and FIG.
FIG. 4 is a main part map of FIG.
【図5】Al−Si系合金の状態図の要部を示す。FIG. 5 shows a main part of a phase diagram of an Al—Si alloy.
【図6】Al合金鋳物の他例の金属組織を示す顕微鏡写
真である。FIG. 6 is a micrograph showing a metal structure of another example of the Al alloy casting.
【図7】(a)は図6の部分拡大写真に相当し、(b)
は(a)の要部写図である。7A is a partially enlarged photograph of FIG. 6, and FIG.
FIG. 4 is a main part map of FIG.
【図8】可動金型の要部側面図である。FIG. 8 is a side view of a main part of the movable mold.
【図9】初晶Si相の体積分率Vfと、流動長比および
シャルピー衝撃値との関係を示すグラフである。FIG. 9 is a graph showing a relationship between a volume fraction Vf of a primary crystal Si phase, a flow length ratio, and a Charpy impact value.
4 キャビティ 5 半溶融Al合金材料(半溶融合金材料) a 示差熱分析曲線 b 第1山形吸熱部 c 第2山形吸熱部 d 上昇開始点 e 下降終了点 4 Cavity 5 Semi-molten Al alloy material (semi-molten alloy material) a Differential thermal analysis curve b 1st chevron heat absorbing part c 2nd chevron heat absorbing part d Ascending start point e Ascending end point
フロントページの続き (51)Int.Cl.6 識別記号 FI C22C 21/02 C22C 21/02 (56)参考文献 特開 平9−85409(JP,A) 特開 平8−192257(JP,A) 特開 平8−112661(JP,A) 特開 平7−100570(JP,A) 特開 平5−200523(JP,A) 特開 平5−312740(JP,A) 特許27947539(JP,B2) (58)調査した分野(Int.Cl.6,DB名) B22D 17/00 B22D 17/32 B22D 27/04 B22D 46/00 C22C 1/02 501 Continuation of the front page (51) Int.Cl. 6 Identification symbol FI C22C 21/02 C22C 21/02 (56) References JP-A-9-85409 (JP, A) JP-A 8-192257 (JP, A) JP-A-8-112661 (JP, A) JP-A-7-100570 (JP, A) JP-A-5-200523 (JP, A) JP-A-5-312740 (JP, A) Patent 27947539 (JP, B2) (58) Fields investigated (Int. Cl. 6 , DB name) B22D 17/00 B22D 17/32 B22D 27/04 B22D 46/00 C22C 1/02 501
Claims (1)
(a)において、共晶溶解による第1山形吸熱部(b)
と、共晶点よりも高融点の成分の溶解による第2山形吸
熱部(c)とが存在する合金材料(5)に加熱処理を施
して、固相と液相とが共存する半溶融合金材料(5)を
調製し、次いで、加圧下で、前記半溶融合金材料(5)
の鋳型キャビティ(4)への充填と、それに次ぐ前記半
溶融合金材料(5)の凝固とを行うチクソキャスティン
グ法において、前記第1山形吸熱部(b)の上昇開始点
(d)の温度をT1 とし、またその下降終了点(e)の
温度をT2 としたとき、前記半溶融合金材料(5)の鋳
造温度TをT1 ≦T≦T2 に設定することを特徴とする
チクソキャスティング法。1. A heat absorption part (b) having a hypoeutectic composition and having a first angle-shaped endothermic part due to eutectic melting in a differential thermal analysis curve (a).
And an alloy material (5) having a second chevron-shaped heat absorbing portion (c) due to the dissolution of a component having a higher melting point than the eutectic point, so that a semi-solid alloy in which a solid phase and a liquid phase coexist is obtained. A material (5) is prepared and then under pressure the semi-solid alloy material (5)
In the thixocasting method of filling the mold cavity (4) with the following and then solidifying the semi-molten alloy material (5), the temperature of the rising start point (d) of the first chevron heat absorbing portion (b) is and T 1, also characterized by setting its lowered end point temperature of (e) when the T 2, wherein the casting temperature T of the semi-molten alloy material (5) to T 1 ≦ T ≦ T 2 thixotropy Casting method.
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7308175A JP2869889B2 (en) | 1995-11-01 | 1995-11-01 | Thixocasting method |
| EP96307358A EP0773302B1 (en) | 1995-10-09 | 1996-10-09 | Thixocasting process |
| US08/728,435 US5993572A (en) | 1995-10-09 | 1996-10-09 | Thixocasting process, and thixocasting aluminum alloy material |
| DE69622664T DE69622664T2 (en) | 1995-10-09 | 1996-10-09 | thixocasting |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7308175A JP2869889B2 (en) | 1995-11-01 | 1995-11-01 | Thixocasting method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH09122867A JPH09122867A (en) | 1997-05-13 |
| JP2869889B2 true JP2869889B2 (en) | 1999-03-10 |
Family
ID=17977816
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP7308175A Expired - Fee Related JP2869889B2 (en) | 1995-10-09 | 1995-11-01 | Thixocasting method |
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| Country | Link |
|---|---|
| JP (1) | JP2869889B2 (en) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5862406B2 (en) * | 2012-03-27 | 2016-02-16 | 株式会社豊田中央研究所 | Aluminum alloy member and manufacturing method thereof |
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- 1995-11-01 JP JP7308175A patent/JP2869889B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
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