JPS6244540A - Manufacture of high-strength aluminum alloy member - Google Patents
Manufacture of high-strength aluminum alloy memberInfo
- Publication number
- JPS6244540A JPS6244540A JP18292485A JP18292485A JPS6244540A JP S6244540 A JPS6244540 A JP S6244540A JP 18292485 A JP18292485 A JP 18292485A JP 18292485 A JP18292485 A JP 18292485A JP S6244540 A JPS6244540 A JP S6244540A
- Authority
- JP
- Japan
- Prior art keywords
- strength
- alloy
- aluminum alloy
- alloys
- hot
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 229910000838 Al alloy Inorganic materials 0.000 title claims abstract description 41
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 11
- 238000001816 cooling Methods 0.000 claims abstract description 20
- 229910052759 nickel Inorganic materials 0.000 claims abstract description 12
- 239000000843 powder Substances 0.000 claims abstract description 12
- 229910052721 tungsten Inorganic materials 0.000 claims abstract description 12
- 239000012535 impurity Substances 0.000 claims abstract description 3
- 238000007712 rapid solidification Methods 0.000 claims description 25
- 239000000203 mixture Substances 0.000 claims description 9
- 229910052782 aluminium Inorganic materials 0.000 claims description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 4
- 229910052748 manganese Inorganic materials 0.000 abstract description 10
- 239000011888 foil Substances 0.000 abstract 1
- 229910045601 alloy Inorganic materials 0.000 description 43
- 239000000956 alloy Substances 0.000 description 43
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 29
- 238000000034 method Methods 0.000 description 26
- 239000011572 manganese Substances 0.000 description 21
- 230000000052 comparative effect Effects 0.000 description 12
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 9
- 230000000694 effects Effects 0.000 description 8
- 239000006104 solid solution Substances 0.000 description 8
- 230000007423 decrease Effects 0.000 description 7
- 230000008569 process Effects 0.000 description 7
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 7
- 239000010937 tungsten Substances 0.000 description 7
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 6
- 238000001125 extrusion Methods 0.000 description 6
- 229910000765 intermetallic Inorganic materials 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 239000000463 material Substances 0.000 description 5
- 238000005979 thermal decomposition reaction Methods 0.000 description 5
- 229910018131 Al-Mn Inorganic materials 0.000 description 4
- 229910018461 Al—Mn Inorganic materials 0.000 description 4
- 229910001080 W alloy Inorganic materials 0.000 description 4
- 229910052786 argon Inorganic materials 0.000 description 3
- 239000002826 coolant Substances 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 238000001192 hot extrusion Methods 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 238000005096 rolling process Methods 0.000 description 3
- 229910018084 Al-Fe Inorganic materials 0.000 description 2
- 229910018192 Al—Fe Inorganic materials 0.000 description 2
- 238000005275 alloying Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 238000005242 forging Methods 0.000 description 2
- 238000009689 gas atomisation Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 238000007725 thermal activation Methods 0.000 description 2
- 229910052723 transition metal Inorganic materials 0.000 description 2
- 229910018134 Al-Mg Inorganic materials 0.000 description 1
- 229910018467 Al—Mg Inorganic materials 0.000 description 1
- 229910000881 Cu alloy Inorganic materials 0.000 description 1
- 229910000914 Mn alloy Inorganic materials 0.000 description 1
- 229910018651 Mn—Ni Inorganic materials 0.000 description 1
- 229910000990 Ni alloy Inorganic materials 0.000 description 1
- 229910009369 Zn Mg Inorganic materials 0.000 description 1
- 229910007573 Zn-Mg Inorganic materials 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 229910002065 alloy metal Inorganic materials 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 101150038956 cup-4 gene Proteins 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000001513 hot isostatic pressing Methods 0.000 description 1
- 238000005098 hot rolling Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 210000003127 knee Anatomy 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 238000010583 slow cooling Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 238000009692 water atomization Methods 0.000 description 1
Landscapes
- Manufacture Of Metal Powder And Suspensions Thereof (AREA)
- Powder Metallurgy (AREA)
Abstract
Description
【発明の詳細な説明】
〔発明の技術分野〕
この発明は、急冷凝固法によシ調製されたアルミニウム
合金凝固体を熱間成形して、高強度の所定形状のアルミ
ニウム合金部材を製造するための、高強度アルミニウム
合金部材の製造方法に関するものである。[Detailed Description of the Invention] [Technical Field of the Invention] The present invention provides a method for producing a high-strength aluminum alloy member of a predetermined shape by hot forming an aluminum alloy solidified body prepared by a rapid solidification method. The present invention relates to a method of manufacturing a high-strength aluminum alloy member.
近年、急冷凝固法によって製造された新種の合金の各方
面への応用が期待されている。急冷凝固法によれば、従
来困難とされていた、合金元素の均一な固溶、過飽和固
溶体の形成および金属間化合物の微細分散化が可能とな
り、さらに、極微細結晶組織や非晶質組織の合金が得ら
れる場合もあるなど、合金の持つ特性を大幅に向上させ
ることができる。In recent years, new types of alloys produced by the rapid solidification method are expected to be applied in various fields. The rapid solidification method enables the formation of uniform solid solutions of alloying elements, the formation of supersaturated solid solutions, and the fine dispersion of intermetallic compounds, which were previously considered difficult. In some cases, alloys can be obtained, and the properties of alloys can be greatly improved.
しかしながら、急冷凝固法は、一般に、溶融状態の少量
の合金を、多量の気体や液体の冷却媒体に接触させるか
、または、高速で移動する冷却された固体表面に流下さ
せて急冷する方法であるから、この方法によって得られ
る凝固金属は、粉末状、薄片状または薄肉す?ン状のよ
うな微小形状にならざるを得ない。However, the rapid solidification method generally involves rapidly cooling a small amount of a molten alloy by contacting it with a large amount of a gaseous or liquid cooling medium, or by causing it to flow down onto a rapidly moving cooled solid surface. The solidified metal obtained by this method can be powdered, flaky or thin-walled. It has no choice but to take on a microscopic shape, such as a cylindrical shape.
従って、このようにして得られた微小形状の凝固金属は
、微小形状のまま使用する特殊用途のほかは、所定の大
きさの部材に加工することが必要とされる。例えば、急
冷凝固法によって製造された微小凝固体状のアルミニウ
ム合金から、構造材用の板材、棒材、形材などのアルミ
ニウム合金部材を製造するためには、一般に、微小凝固
体状のアルミニウム合金を集めそして圧縮することによ
り予備成形体を調製し、次いで、この予備成形体に対し
、圧延、押出し、鍛造などの展伸による成形加工を施す
成形加工工程が必要とされる。Therefore, the microscopic solidified metal thus obtained needs to be processed into a member of a predetermined size, except for special purposes in which it is used in its microscopic shape. For example, in order to manufacture aluminum alloy members such as plates, bars, and profiles for structural materials from microsolidified aluminum alloys produced by the rapid solidification method, microsolidified aluminum alloys are generally used. A forming process is required in which a preform is prepared by collecting and compressing the preform, and then the preform is subjected to a forming process by stretching such as rolling, extrusion, or forging.
上述した成形加工工程は、微小形状の凝固金属同士の熱
的活性化による強固な固着、および、成形、加工時の動
力低減の観点から、熱間で行うことが好ましい。しかし
ながら、熱間で成形加工を行なうと、急冷凝固によって
形成、された好ましい非平衡組織が、熱的活性化により
平衡状態に復帰する結果、折角、急冷凝固によって得ら
れた特性の大半が消失する問題がある。これは、急冷凝
固によって形成された過飽和固溶体が、吐濃度の固溶体
と金属間化合物とに熱分解し、また、微品質組織が粗大
化することによって、急冷凝固組織が変質するためであ
る。The above-mentioned forming process is preferably carried out hot from the viewpoints of firm adhesion of micro-shaped solidified metals by thermal activation and reduction of power during forming and processing. However, when hot forming is performed, the favorable non-equilibrium structure formed by rapid solidification returns to an equilibrium state through thermal activation, resulting in the loss of most of the properties obtained by rapid solidification. There's a problem. This is because the supersaturated solid solution formed by rapid solidification thermally decomposes into a solid solution and an intermetallic compound at the same concentration, and the fine quality structure becomes coarser, thereby altering the quality of the rapidly solidified structure.
従来の溶解鋳造法によって製造されるアルミニウム合金
の場合、Feなどの遷移金属元素の固溶量は、平衡状態
で約Q、1wt、%であるが、急冷凝固アルミニウム合
金の場合は約IQwt、%まで増加される。従って、急
冷凝固アルミニウム合金の粉末や薄片では、グイツカー
ス硬度が200以上を示すものが比較的容易に得られ、
薄肉リボン状の急冷凝固アルミニウム合金をそのまま引
張り試験に供すれば、50Kqf/m−以上の引張シ強
さが示される。しかしながら、このような微小凝固体状
の急冷凝固アルミニウム合金に対し、熱間展伸加工を含
む成形加工を施して、所定形状の部材に成形した場合は
、その部材のヴイツカース硬度は約100に、そして、
引張り強さは約30Kgf/m−にまで低下し、急冷凝
固によって得られた高硬度および高強度特性が失われる
。In the case of aluminum alloys manufactured by conventional melting and casting methods, the amount of solid solution of transition metal elements such as Fe is approximately Q, 1wt,% in the equilibrium state, whereas in the case of rapidly solidified aluminum alloys, it is approximately IQwt,%. will be increased to Therefore, it is relatively easy to obtain rapidly solidified aluminum alloy powders and flakes with a Guitzkaas hardness of 200 or more.
If a thin ribbon-shaped rapidly solidified aluminum alloy is directly subjected to a tensile test, it will exhibit a tensile strength of 50 Kqf/m- or more. However, when such a rapidly solidified aluminum alloy in the form of a microsolid is subjected to forming processing including hot stretching to form a member into a predetermined shape, the Witzkars hardness of the member is approximately 100. and,
The tensile strength decreases to about 30 Kgf/m- and the high hardness and high strength properties obtained by rapid solidification are lost.
このような硬度および強度の低下を防止するために、成
形加工を冷間で行うと、アルミニウム合金に特有の強固
な表面酸化皮膜が、微小凝固体間の固着を妨げるので、
良質な成形部材を得ることができない。そこで、上記成
形加工を、200〜300℃の温度のいわゆる温間で行
えば、急冷凝固組織の熱分解が比較的少なく、微小凝固
体間の固着も可能であるが、一方、成形のために大きな
力を要するため、得られる成形部材の寸法および形状が
限定され、且つ、成形のために特別な装置が必要とされ
るので、実用的ではない。In order to prevent such a decrease in hardness and strength, if the forming process is performed cold, the strong surface oxide film unique to aluminum alloys will prevent the microsolids from adhering to each other.
It is not possible to obtain high-quality molded parts. Therefore, if the above-mentioned forming process is performed at a temperature of 200 to 300°C, so-called warm temperature, there will be relatively little thermal decomposition of the rapidly solidified structure and it will be possible to fix the microsolids, but on the other hand, for forming The large force required limits the size and shape of the molded part obtained, and special equipment is required for molding, making it impractical.
従って、この発明の目的は、急冷凝固法により高強度ア
ルミニウム合金部材を製造するに当シ、熱間で展伸加工
を施しても強度の低下が生ずることがなく、急冷凝固に
よって得られた優れた特性が保持され、しかも、適度の
延性を有する高強度アルミニウム合金部材を製造するだ
めの方法を提供することにある。Therefore, it is an object of the present invention to produce high-strength aluminum alloy members by the rapid solidification method, without causing a decrease in strength even when subjected to hot drawing, and to achieve the excellent properties obtained by rapid solidification. The object of the present invention is to provide an alternative method for manufacturing a high-strength aluminum alloy member that retains its properties and has appropriate ductility.
本発明者等は、急冷凝固法によって、高強度アルミニウ
ム合金部材を製造するに当り、熱間で展伸加工を施して
も強度の低下が生ずることがなく、急冷凝固によって得
られた優れた特性が保持される方法を開発すべく鋭意研
究を重ねた。In manufacturing high-strength aluminum alloy members by the rapid solidification method, the present inventors have discovered that there is no decrease in strength even when hot drawing is performed, and that the excellent properties obtained by rapid solidification are excellent. Intensive research was conducted to develop a method that would preserve this.
その結果、本発明者等は、先に、所定量のマンガンおよ
びタングステンを含有するアルミニウム合金は、急冷凝
固によってその硬度および強度が高められると共に、こ
の急冷凝固によって得られた特性は、所定温度範囲での
熱間成形を行なった場合に、殆ど変化しないことを知見
した。As a result, the present inventors have previously discovered that the hardness and strength of an aluminum alloy containing a predetermined amount of manganese and tungsten can be increased by rapid solidification, and that the properties obtained by this rapid solidification can be improved within a predetermined temperature range. It was found that there was almost no change when hot forming was performed.
とのA/ −Mn−W合金の急冷凝固体を熱間成形して
得られたアルミニウム合金部材は、著しく高い硬度およ
び強度を有するが、その後の研究の結果、前記アルミニ
ウム合金部材または例えば熱間押し出しに供するビレッ
トのようなAl−Mn−W合金の予備成形体が大型にな
ると、その延性が低下し、実用上必ずしも満足し得る延
性を有する高強度アルミニウム合金部材の得られないこ
とがわかった。An aluminum alloy member obtained by hot forming a rapidly solidified body of A/-Mn-W alloy with It has been found that when a preformed Al-Mn-W alloy such as a billet used for extrusion becomes large, its ductility decreases, making it impossible to obtain a high-strength aluminum alloy member with ductility that is necessarily satisfactory for practical use. .
そこで、本発明者等は、上述した問題を解決すべく更に
研究を重ねた結果、マンガンの一部を所定量のニッケル
で置換すれば、熱間加工後の強度ばAl−Mn−W合金
以上であって、しかも延性が大幅に改善され、引張シ伸
びが2倍以上になることを知見した。Therefore, as a result of further research to solve the above-mentioned problems, the present inventors have found that if a part of manganese is replaced with a predetermined amount of nickel, the strength after hot working will be higher than that of Al-Mn-W alloy. Moreover, it was found that the ductility was significantly improved and the tensile elongation was more than doubled.
この発明は、上記知見に基いてなされたものであって、
Mn : 4.0〜12 wt、%、
W:0.2〜4.Qwt、チ、
Ni : 0.5〜4.Qwt、係、
但し、Mn十Nlは、8〜14Wt、%、残シ:アルミ
ニウムおよび不可避不純物からなる成分組成を有するア
ルミニウム合金を溶製し、
次いで、前記アルミニウム合金を、103℃/sec以
下の冷却速度で急冷凝固して、粉末状または薄片状の凝
固体を調製し、
このようにして得られた凝固体を、そのまま、または予
備成形した上、少なくとも一度は500°C以下の温度
で熱間成形し、かくして、所定形状の高強度を有するア
ルミニウム合金部材を製造することに特徴を有するもの
である。This invention was made based on the above findings, and includes: Mn: 4.0-12 wt.%, W: 0.2-4. Qwt, Chi, Ni: 0.5-4. Qwt, however, Mn + Nl is 8 to 14 Wt%, the balance is aluminum and unavoidable impurities. A powder or flake solidified body is prepared by rapid solidification at a cooling rate, and the solidified body thus obtained is heated at least once at a temperature of 500°C or less, either as it is or after being preformed. The method is characterized in that an aluminum alloy member having a predetermined shape and high strength is produced by interforming.
この発明において、アルミニウム合金の化学成分組成範
囲を上述のように限定した理由について以下に述べる。In this invention, the reason why the chemical composition range of the aluminum alloy is limited as described above will be described below.
(1) マンガン(Mn)
マンガンは、鉄などと共に遷移金属元素であり、急冷凝
固法によりアルミニウム中に過飽和に固溶または微細に
分散析出させると、強度が著しく向上する作用を有して
いる。また、熱拡散が遅いので、AA−Mn合金は熱的
安定性に優れ、約300°Cまでの高温において高い強
度を示す。Al −Mn合金をAl−Fe合金と比較す
ると、Al−Mn合金は、Al、−1;’e 合金より
ほい冷却速度でも過飽和固溶体が形成されやすく、融点
が低いので溶解作業が容易であり、高い弾性率が得られ
、且つ、耐食性に優れるなどAl−Fe合金よυも優れ
た性質を有している。(1) Manganese (Mn) Manganese is a transition metal element along with iron and the like, and when it is precipitated as a supersaturated solid solution or finely dispersed in aluminum by the rapid solidification method, it has the effect of significantly improving the strength. Additionally, due to slow thermal diffusion, AA-Mn alloys have excellent thermal stability and exhibit high strength at high temperatures up to about 300°C. Comparing the Al-Mn alloy with the Al-Fe alloy, the Al-Mn alloy tends to form a supersaturated solid solution even at a lower cooling rate than the Al, -1;'e alloy, and its melting point is lower, making it easier to melt. It has properties superior to Al-Fe alloys, such as high elastic modulus and excellent corrosion resistance.
マンガンの含有量が4.Owt、1未満では、上述した
作用に所望の効果が得られず、一方、マンガンの含有量
が12wt、%を超えても上述した作用に格別の向上が
現われず、逆に金属間化合物の生成量が多過ぎて延性が
低下する問題が生ずる。従って、マンガンの含有量は、
4.0から12Wt、%の範囲内に限定すべきである。Manganese content is 4. If the manganese content is less than 1, the desired effect cannot be obtained in the above-mentioned action, and on the other hand, even if the manganese content exceeds 12 wt. If the amount is too large, a problem arises in that ductility decreases. Therefore, the manganese content is
It should be limited within the range of 4.0 to 12 Wt,%.
(2) タングステン(W)
Al−Mn合金は、上述した優れた特性を有しているが
、急冷凝固後に行なわれる熱間成形加工において、熱分
解により上記特性が大きく低下する問題を有している。(2) Tungsten (W) Al-Mn alloy has the above-mentioned excellent properties, but it has the problem that the above-mentioned properties are significantly reduced due to thermal decomposition during hot forming processing performed after rapid solidification. There is.
タングステンは、Al −Mn 合金が持つ上記問題を
解決するものであり、タングステンの添加によって、急
冷凝固の際に生ずる急冷凝固組織の熱分解を緩慢にし、
急冷凝固と熱間成形加工との組合せによるアルミニウム
合金部材の強度を著しく向上させる作用を有している。Tungsten solves the above-mentioned problems of Al-Mn alloys, and the addition of tungsten slows down the thermal decomposition of the rapidly solidified structure that occurs during rapid solidification.
It has the effect of significantly improving the strength of aluminum alloy members due to the combination of rapid solidification and hot forming.
タングステンの含有量が0.2 wt、% 未満では
、上述した作用に所望の効果が得られず、一方、タング
ステンの含有量が4.0wt、%を超えると、金属間化
合物の生成量が多過ぎて延性が低下する問題が生ずる。If the tungsten content is less than 0.2 wt.%, the desired effect described above cannot be obtained, while if the tungsten content exceeds 4.0 wt.%, a large amount of intermetallic compounds will be produced. If the thickness is too high, a problem arises in which ductility decreases.
従って、タングステンの含有量は、0.2から4.Ow
t、%の範囲内とすべきである。Therefore, the tungsten content is between 0.2 and 4. Ow
t, should be within the range of %.
(3) ニッケル(Ni)
ニッケルは、マンガンと同じく強度を向上させる作用を
有している。更に、Al−Mn−W合金にニッケルを添
加することによって、急冷凝固と熱間成形加工との組合
せによるアルミニウム合金部材の延性を著しく向上させ
、特に、マンガンの一部をニッケルに置換すると、強度
も若干向上するが、引張り伸びが2倍以上になるほどの
延性向上作用がある。(3) Nickel (Ni) Nickel, like manganese, has the effect of improving strength. Furthermore, by adding nickel to the Al-Mn-W alloy, the ductility of the aluminum alloy member by a combination of rapid solidification and hot forming is significantly improved, and in particular, when part of the manganese is replaced with nickel, the strength is increased. However, the ductility is improved to the extent that the tensile elongation is more than doubled.
ニッケルの含有量がQ、5wt、1未満では、上述した
作用に所望の効果が得られず、一方、ニッケルの含有量
が4.Qwt、%を超えると、Al−Mn −Ni 金
属間化合物の生成量が多過ぎて、かえって延性が低下す
る問題が生ずる。従って、ニッケルの含有量は、0.5
から4.Qwt、%の範囲内とすべきである。If the nickel content is less than Q, 5wt, 1, the desired effect described above cannot be obtained; on the other hand, if the nickel content is less than 4wt. When Qwt, % is exceeded, the amount of Al-Mn-Ni intermetallic compounds produced is too large, resulting in a problem of lowering the ductility. Therefore, the nickel content is 0.5
From 4. Qwt, should be within the range of %.
(4) (Mn 十Ni )量
上述のように、急冷凝固されたアルミニウム合金の強度
は、(Mn+Ni)量によって定″!シ、タングステン
の作用によって、その強度が熱間成形加工されたアルミ
ニウム合金部材においても保持される。(4) Amount of (Mn + Ni) As mentioned above, the strength of a rapidly solidified aluminum alloy is determined by the amount of (Mn + Ni)! It is also retained in the member.
(Mn+Ni)量が8wt、係未満では所望の強度が得
られず、一方、(Mn+Ni)量が14Wt、%を超え
ると、金属間化合物の生成量が多過ぎて延性が低下する
問題が生ずる。従って、(Mn+Ni)量は、8から1
4wt、%の範囲内とすべきである。If the amount of (Mn+Ni) is less than 8 wt.%, the desired strength cannot be obtained. On the other hand, if the amount of (Mn+Ni) exceeds 14 wt.%, the amount of intermetallic compounds produced is too large, resulting in a problem of decreased ductility. Therefore, the amount of (Mn+Ni) is from 8 to 1
It should be within the range of 4wt.%.
上述した成分組成範囲のAA! −Mn −W−Ni合
金は、溶融状態からの急冷凝固によって、高い強度特性
が発揮されるが、その冷却速度は、103℃/see以
上とすべきでちる。即ち、上記成分組成の溶製されたア
ルミニウム合金を、103℃/sec以上の冷却速度で
急冷して得られた粉末状または薄片状の凝固体を熱間成
形することにより、従来の高強度アルミニウム合金に匹
敵する室温強度と、従来合金を上回る耐熱性および剛性
を有する高強度アルミニウム合金部材が得られる。AA within the above-mentioned composition range! -Mn-W-Ni alloy exhibits high strength properties by rapid solidification from a molten state, but the cooling rate should be 103° C./see or higher. That is, by rapidly cooling a melted aluminum alloy having the above-mentioned composition at a cooling rate of 103° C./sec or higher and hot forming a powdery or flaky solidified body, conventional high-strength aluminum can be produced. A high-strength aluminum alloy member can be obtained that has room temperature strength comparable to alloys and heat resistance and rigidity that exceed conventional alloys.
冷却速度が103°C/SeC未満では、合金元素が十
分に固溶せず、粗大な金属間化合物が析出するので熱間
成形加工によって優れた強度および延性を有する合金部
材を得ることができない。なお、回転ロール法などの手
段によシ、105℃/See以上の冷却速度で急冷凝固
された粉末、薄片を使用しても、熱間成形加工された合
金部材の強度は殆ど向上せず、むしろ急冷凝固法の経済
性が悪く、製造費用の増大を招くことに注意すべきであ
る。If the cooling rate is less than 103° C./SeC, the alloying elements will not form a sufficient solid solution and coarse intermetallic compounds will precipitate, making it impossible to obtain an alloy member with excellent strength and ductility through hot forming. In addition, even if powder or flakes that have been rapidly solidified at a cooling rate of 105°C/See or the like by means such as a rotating roll method are used, the strength of the hot-formed alloy member will hardly be improved; Rather, it should be noted that the rapid solidification method is not economical and increases manufacturing costs.
通常のガス・アトマイズ法や水アトマイズ法による冷却
速度は、102〜104°Q/Sec であシ、改良
されたガス・アトマイズ法や回転ロール法による冷却速
度は、104〜b
急冷凝固手段は、上述した公知の方法によって行なうこ
とができる。The cooling rate by ordinary gas atomization method or water atomization method is 102 to 104°Q/Sec, and the cooling rate by improved gas atomization method or rotating roll method is 104 to b. This can be done by the known methods mentioned above.
上記のような条件による急冷凝固によって得られた粉末
状、薄片状の凝固体、あるいは、薄肉リボンを裁断した
薄片状の微小凝固体、または、必要に応じてよシ細かく
粉砕した粉体を、そのまままたは予備成形した後、板材
、棒材、形材等、所要の形状に成形するだめの成形加工
を、少なくとも一度は熱間で行なうことが必要である。Powder-like, flaky solidified material obtained by rapid solidification under the above conditions, or flaky micro-solidified material obtained by cutting a thin ribbon, or finely ground powder as required, It is necessary to hot-form the material as it is or after preforming it into a desired shape, such as a plate, bar, profile, etc., at least once.
このような熱間成形加工は、熱間ゾレス、熱間静水圧プ
レス(HIP)、熱間圧延、熱間押出し、熱間鍛造など
公知の手段によって行なうことができる。Such hot forming processing can be performed by known means such as hot Soles, hot isostatic pressing (HIP), hot rolling, hot extrusion, and hot forging.
熱間成形加工時の加工温度は、500℃以下とすべきで
ある。即ち、加工温度が500℃を超えると、急冷凝固
組織が急速に熱分解する結果、所望の強度が得られない
。好ましい温度範囲は350〜480℃であって、この
温度範囲で成形加工を行えば、急冷凝固組織の熱分解が
ほぼ抑制され、成形された合金部材は、実用的に有意義
な強度特性を示し、且つ、一般に工業的に使用されてい
る成形加工装置の能力を超えることはない。The processing temperature during hot forming should be 500°C or less. That is, when the processing temperature exceeds 500°C, the rapidly solidified structure undergoes rapid thermal decomposition, making it impossible to obtain the desired strength. The preferred temperature range is 350 to 480°C, and if the forming process is performed in this temperature range, thermal decomposition of the rapidly solidified structure is almost suppressed, and the formed alloy member exhibits practically meaningful strength characteristics. In addition, it does not exceed the capabilities of molding equipment that is generally used industrially.
実施例1
第1表に示す本発明の範囲内の成分組成を有する2種類
の合金A、Bを溶製した。この合金A。Example 1 Two types of alloys A and B having compositions within the range of the present invention shown in Table 1 were melted. This alloy A.
Bを各々再溶解し、その溶湯に冷却媒体としてのアルゴ
ンガスを吹き付けてアトマイズし、アトマイズ条件の設
定およびアトマイズ粉末の篩い分けにより、次の2種類
の急冷凝固粉末を調製した。B was re-melted, the molten metal was atomized by spraying argon gas as a cooling medium, and the following two types of rapidly solidified powders were prepared by setting atomization conditions and sieving the atomized powder.
(1)冷却速度: l O2〜10”C/sec未満粒
径:32〜100メツシユ(500〜150μm)(2
)冷却速度:103〜b
粒径ニー100メツシュ(平均粒径約44μm)上述の
急冷凝固粉末を、400℃の温度で熱間プレスし、直径
150語のビレットに予備成形した。次いで上述のビレ
ットを、450から510℃の温度で、押出し比25に
よシ熱間押出し成形し、直径30ttILの丸棒を製造
した。(1) Cooling rate: 1 O2~less than 10"C/sec Particle size: 32~100 mesh (500~150μm) (2
) Cooling rate: 103-b Particle size knee 100 mesh (average particle size about 44 μm) The above-mentioned rapidly solidified powder was hot pressed at a temperature of 400° C. and preformed into a billet with a diameter of 150 words. The billet described above was then hot extruded at a temperature of 450 to 510° C. and an extrusion ratio of 25 to produce a round bar with a diameter of 30 ttIL.
第2表は、このようにして製造した本発明合金A1〜4
および比較合金屋1〜4の成分組成、急冷凝固粉末の冷
却速度、熱間押出しの際の押出し温度、および、室温で
の引張り性質である。比較合金扁lおよびA2は、冷却
速度が本発明の範囲を外れて遅く、比較合金A3および
A4は、熱間押出しによる成形加工温度が本発明範囲を
外れて高い。Table 2 shows the alloys A1-4 of the present invention produced in this way.
and the component compositions of comparative alloys 1 to 4, the cooling rate of the rapidly solidified powder, the extrusion temperature during hot extrusion, and the tensile properties at room temperature. Comparative alloy flats I and A2 have slow cooling rates that are outside the range of the present invention, and comparative alloys A3 and A4 have high forming temperatures by hot extrusion that are outside the range of the present invention.
第1表
上記第2表から明らかなように、本発明合金屋1〜4は
、引張シ強さおよび伸びが共に優れている。これに対し
て、比較合金A1およびA2は、冷却速度が本発明の範
囲を外れて遅いため、引張り強さが圓い。まだ、比較合
金属3および盃4は、成形加工温度(押出し温度)が本
発明の範囲を外れて高いため、引張シ強さおよび伸びが
共に吐い。Table 1 As is clear from Table 2 above, alloys 1 to 4 of the present invention are excellent in both tensile strength and elongation. On the other hand, comparative alloys A1 and A2 have rounded tensile strengths because their cooling rates are slow and out of the range of the present invention. However, comparative alloy metal 3 and cup 4 had a high molding temperature (extrusion temperature) outside the range of the present invention, so both tensile strength and elongation were poor.
実施例2
第3表に示すように、本発明の範囲内の成分組成を有す
る本発明合金A5〜10および本発明の範囲外の成分組
成を有する比較合金A5〜I4を溶製した。これらの合
金を再溶解し、その溶湯を冷却媒体としてのアルゴンガ
スの吹き付けによるアルゴンガス・アトマイズにょシ、
急冷し凝固せしめ、ふるい分けして、−100メツシユ
の急冷凝固粉末を調製した。その冷却速度は103〜1
0”’C/seeであった。Example 2 As shown in Table 3, inventive alloys A5 to 10 having component compositions within the range of the present invention and comparative alloys A5 to I4 having component compositions outside the range of the present invention were melted. These alloys are remelted and the molten metal is argon gas atomized by spraying argon gas as a cooling medium.
The mixture was rapidly cooled, solidified, and sieved to prepare a -100 mesh rapidly solidified powder. Its cooling rate is 103~1
It was 0'''C/see.
この急冷凝固粉末を、400 ’Cの温度で熱間プレス
し、直径15011Bのビレットに予備成形した。This rapidly solidified powder was hot pressed at a temperature of 400'C and preformed into a billet with a diameter of 15011B.
次いで上述のビレットを、450 ℃の温度で、押出し
比25によ多熱間押出し成形し、直径301111の丸
棒を製造した。第3表には、このようにして製造されだ
丸棒の室温での引張り強さおよび伸び、ならびに、25
0℃における引張シ強さが併せて示されている。The billet described above was then multi-hot extruded at a temperature of 450° C. and an extrusion ratio of 25 to produce a round bar with a diameter of 301,111 mm. Table 3 shows the tensile strength and elongation at room temperature of the round bars produced in this way, as well as the
The tensile strength at 0°C is also shown.
比較合金A5はMnの含有量が本発明の範囲外である。Comparative alloy A5 has a Mn content outside the range of the present invention.
比較合金属6およびA8はWを含有せず、扁7はNiを
含有していない。比較合金通9はNiの含有量が本発明
の範囲外である。比較合金AIOはWおよびNiを含有
せず、A 11はNi を含有していない。比較合金
A I 2はWの含有量が本発明の範囲外であり、A
13はMn+Ni の含有量が本発明の範囲外であり、
そして、A14はMn の含有量およびMn十Niの
含有量が本発明の範囲外である。Comparative metal alloys 6 and A8 do not contain W, and flat metal 7 does not contain Ni. Comparative Alloy No. 9 has a Ni content outside the range of the present invention. Comparative alloy AIO does not contain W and Ni, and A 11 does not contain Ni. Comparative alloy A I 2 has a W content outside the range of the present invention, and A
No. 13 has a Mn+Ni content outside the scope of the present invention,
In A14, the Mn content and the Mn+Ni content are outside the scope of the present invention.
第3表から明らかなように、本発明合金屋5〜10は、
何れも高い引張り強さと適度の伸びを有しており、その
室温強度は、従来の溶解鋳造法による展伸用アルミニウ
ム合金の中でも高強度合金である2000番台の合金(
AI−Cu系合金)および7000番台の合金(Al−
Zn−Mg系合金)の強度に匹敵する。また、従来の展
伸用アルミニウム合金の中で比較的高い高温強度を有す
る合金は、上記2000番台の合金および5000番台
の合金(Al −Mg 系合金)であシ、これらの合金
の250℃における引張シ強さは、15Kgf/mm’
以下である。As is clear from Table 3, the alloy shops 5 to 10 of the present invention are
All of them have high tensile strength and moderate elongation, and their room temperature strength is comparable to that of the 2000 series alloy (
AI-Cu alloy) and 7000 series alloy (Al-
Comparable to the strength of Zn-Mg alloy). In addition, among conventional aluminum alloys for wrought use, alloys with relatively high high temperature strength are the above-mentioned 2000 series alloys and 5000 series alloys (Al-Mg alloys). Tensile strength is 15Kgf/mm'
It is as follows.
これに対して、本発明合金の250°Cにおける引張り
強さは25Kpf/mm’ 以上であり、従来のアル
ミニウム合金に比べて極めて高い高温強度を有している
。一方、本発明の範囲外の比較合金A5〜14は、何れ
も引張シ強さまたは伸びが劣っておシ、実用性が大幅に
低下している。On the other hand, the tensile strength of the alloy of the present invention at 250°C is 25 Kpf/mm' or more, and has extremely high high temperature strength compared to conventional aluminum alloys. On the other hand, comparative alloys A5 to A14, which are outside the scope of the present invention, are all inferior in tensile strength or elongation, and are significantly less practical.
以上詳述したように、この発明の方法によれば、従来の
高強度展伸用アルミニウム合金である2000番台合金
および7000番台合金に匹敵する室温強度と、従来の
アルミニウム合金に比べて極めて高い高温強度を有し、
しかも適度の伸びを有するアルミニウム合金部材を製造
することができ、且つ、その製造は、従来の溶解鋳造材
と同様の熱間成形加工によって行なうことができるので
、広範囲の応用が可能である等、幾多の工業上優れた効
果がもたらされる。As detailed above, according to the method of the present invention, it is possible to achieve room temperature strength comparable to conventional high-strength aluminum alloys such as 2000 series alloys and 7000 series alloys, and extremely high temperature strength compared to conventional aluminum alloys. Has strength,
In addition, it is possible to produce aluminum alloy members with appropriate elongation, and the production can be carried out by the same hot forming process as conventional melt-casting materials, so it can be used in a wide range of applications. Many industrially excellent effects are brought about.
Claims (1)
以上の冷却速度で急冷凝固して、粉末状または薄片状の
凝固体を調製し、 このようにして得られた凝固体を、そのまま、または予
備成形した上、少なくとも一度は500℃以下の温度で
熱間成形し、かくして、所定形状の高強度を有するアル
ミニウム合金部材を製造することを特徴とする高強度ア
ルミニウム合金部材の製造方法。[Claims] Mn: 4.0 to 12wt. %, W: 0.2-4.0wt. %, Ni: 0.5-4.0wt. %, however, Mn+Ni is 8 to 14 wt. %, Remaining: An aluminum alloy having a composition consisting of aluminum and unavoidable impurities is melted, and then the aluminum alloy is heated at 10^3°C/sec.
Rapid solidification is performed at the above cooling rate to prepare a powder or flaky solidified body, and the solidified body thus obtained is heated as it is or after being preformed at least once at a temperature of 500°C or less. A method for producing a high-strength aluminum alloy member, which comprises hot forming and thus producing an aluminum alloy member having a predetermined shape and high strength.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18292485A JPS6244540A (en) | 1985-08-22 | 1985-08-22 | Manufacture of high-strength aluminum alloy member |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18292485A JPS6244540A (en) | 1985-08-22 | 1985-08-22 | Manufacture of high-strength aluminum alloy member |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6244540A true JPS6244540A (en) | 1987-02-26 |
| JPH0478697B2 JPH0478697B2 (en) | 1992-12-11 |
Family
ID=16126754
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP18292485A Granted JPS6244540A (en) | 1985-08-22 | 1985-08-22 | Manufacture of high-strength aluminum alloy member |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6244540A (en) |
-
1985
- 1985-08-22 JP JP18292485A patent/JPS6244540A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0478697B2 (en) | 1992-12-11 |
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