TW200533763A - Aluminum alloy for plastic working, and its manufacturing method - Google Patents

Aluminum alloy for plastic working, and its manufacturing method Download PDF

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TW200533763A
TW200533763A TW094106839A TW94106839A TW200533763A TW 200533763 A TW200533763 A TW 200533763A TW 094106839 A TW094106839 A TW 094106839A TW 94106839 A TW94106839 A TW 94106839A TW 200533763 A TW200533763 A TW 200533763A
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aluminum alloy
room temperature
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alloy powder
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TW094106839A
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Chinese (zh)
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Shigeru Okaniwa
Hideki Ishii
Takashi Kajiyama
Takutoshi Kondo
Manabu Imaoka
Kenji Tsubouchi
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Shimano Kk
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Abstract

The objective of the present invention is to provide an aluminum alloy for plastic working, which are useful for high performance members, such as automotive parts, fishing gears, golf clubs and snow boards, and has high tensile strength, high Young's modulus and high ductility, and to provide its manufacturing method. A powder mixture is prepared by mixing 10 to 25wt.% alumina with an aluminum alloy powder having a composition consisting of, by weight, 0.4 to 2.0% Si, 0.4 to 2.0% Mg, 0.5 to 2.0%, in total, of one or more elements selected from among Fe, Mn and Cr, and the balance Al with inevitable impurities. The powder mixture is compacted at room temperature, and the resultant green compact is vacuum degassed at 200 to 450 DEG C and further sintered at a high temperature of 500 to 600 DEG C. The resultant sintered compact is pressure sintered and then forged. By this method, a structural member as a finished product having ≥ 80 GPa Young's modulus at room temperature, ≥ 300 MPa tensile strength at room temperature after water quenching treatment and ≥ 5% elongation can be obtained.

Description

200533763 (1) 九、發明說明 【發明所屬之技術領域】 本發明是關於作爲自行車構件、釣具、高爾夫球桿及 滑雪板等高機能材料之高拉伸強度、高彈性係數及高延展 性的塑性加工用鋁合金及其製造方法。 【先前技術】 I 近來,嘗試將陶瓷添加分散於利用急冷凝固法所獲得 的鋁合金粉末中,以期能提高其特性、特別是剛性的提昇 。舉例來說,檢討A1-高Si系、Al-Fe-Mo系、Al-Cu系、 Al-Si-Mg系或者Al-Zn-Mg系的組成(請參考專利文獻1 )° 此外,當對鋁合金進行押出或鍛造等加熱成形加工時 ,由前置冷加工步驟所獲得之壓粉成形的粉末成型體內部 或表面含有水合物(hydrate )和空氣,倘若直接實施熱 φ 加工,有時會於熱加工或後續的熱處理步驟中產生氣泡( 蓬鬆)之類的缺失。由於上述的原因,爲避免缺失的形成 ’一般是在熱加工之前執行脫氣。 [專利文獻1] 日本第2 5 4 6 6 6 0號專利公報(申請專利範圍) 【發明內容】 [發明欲解決之課題] 在傳統的鋁合金中,譬如自行車構件、釣具、高爾夫 200533763 (2) 球桿及滑雪板等高機能材料具有無法充分獲得有效的高拉 伸強度、局彈性係數及高延展性的問體。 本發明是有鑑於上述問題所硏發的發明,本發明的課 題爲提供一種··作爲自行車構件、釣具、高爾夫球桿及滑 雪板等高機能材料之高拉伸強度、高彈性係數及高延展性 的塑性加工用鋁合金及其製造方法。 [解決課題之手段] 爲了解決上述課題,本案申請專利範圍第1項所記載 的發明’其特徵爲:是由:0.4〜2.0重量%的Si、0.4〜2.0 重量%的Mg;和由含有從Fe、Mn、Cr中選出一種以上 合計0.5〜2_0重量% ,且剩餘部分含有無法避免之不純物 的A1所形成的鋁合金粉末;及i 〇〜25重量%的氧化鋁所混 合而成的固化成形材,室溫狀態下的彈性係數爲8〇GPa以 上’水淬處理(water quenching )後的室溫拉伸強度爲 3 00MPa以上,且延展性爲5%以上。 本案申請專利範圍第2項所記載的發明,爲申請專利 範圍第1項所記載的塑性加工用鋁合金,其中上述的銘合 金粉末,是由含有·· 0.4〜2.0重量°/Q的si、0.4〜2.0重量% 的Mg、0.10〜0.3重量%的Fe、〇·〇5〜0.6重量%的Μη、 0·05〜0.6重量%之Cr的Α1所形成的合金粉末。 在本案中,Si的添加量形成0.4〜2.0重量%的原因爲 :Si的添加將與Mg形成化合物Mg2Si,欲使鋁基質於熱 處理後的強度爲3 00MPa以上所需的最低添加量〇.4重量% 200533763 (3) ,而一旦Si的添加量超過2.0重量% ,將無法獲得5%以 上的拉伸性,導致鍛造加工上出現問題之故。 此外,Mg的添加量形成0.4〜2.0重量%的原因爲:爲 了形成可提高熱處理後強度之Si的化合物Mg2Si而需要 添加Mg,爲了獲得3 00MPa以上的拉伸強度所需的最低添 加量爲〇·4重量% ,而一旦Mg的添加量超過2.0重量% , 將降低塑性加工性。200533763 (1) IX. Description of the invention [Technical field to which the invention belongs] The present invention relates to plastic processing with high tensile strength, high elastic coefficient, and high ductility as high-performance materials such as bicycle components, fishing tackles, golf clubs, and snowboards. Use aluminum alloy and its manufacturing method. [Previous technology] I Recently, attempts have been made to add and disperse ceramics in aluminum alloy powder obtained by the rapid solidification method in order to improve its characteristics, especially rigidity. For example, review the composition of A1-high Si-based, Al-Fe-Mo-based, Al-Cu-based, Al-Si-Mg-based, or Al-Zn-Mg-based (see Patent Document 1) ° In addition, when the When the aluminum alloy is subjected to hot forming processing such as extrusion or forging, the powder formed body obtained by the pre-cold working step contains hydrate and air inside or on the surface. If hot φ processing is directly performed, it may sometimes occur in Defects such as air bubbles (fluffy) are generated during thermal processing or subsequent heat treatment steps. For the reasons described above, in order to avoid the formation of a defect ', degassing is generally performed before hot working. [Patent Document 1] Japanese Patent Bulletin No. 2 5 4 6 6 60 (Scope of patent application) [Summary of the Invention] [Questions to be Solved by the Invention] In traditional aluminum alloys, such as bicycle components, fishing tackles, and golf 200533763 (2 High-performance materials such as clubs and snowboards have problems that cannot effectively obtain effective high tensile strength, local elastic coefficient, and high ductility. The present invention has been developed in view of the above problems, and an object of the present invention is to provide a high tensile strength, a high elastic coefficient, and a high ductility as high-performance materials such as bicycle members, fishing tackles, golf clubs, and snowboards. Aluminum alloy for plastic processing and manufacturing method thereof. [Means for Solving the Problems] In order to solve the above problems, the invention described in the first patent application scope of the present application is characterized in that: it is composed of: 0.4 to 2.0% by weight of Si, 0.4 to 2.0% by weight of Mg; and One or more of Fe, Mn, and Cr are selected from a total of 0.5 to 2_0% by weight, and the remainder contains unavoidable impurities of A1, which is an aluminum alloy powder formed of A1; and i 0 to 25% by weight of alumina is solidified and mixed. Material, the coefficient of elasticity at room temperature is 80 GPa or more, and the room temperature tensile strength after water quenching is 300 MPa or more, and the ductility is 5% or more. The invention described in the second patent application scope of this case is an aluminum alloy for plastic working as described in the first patent application scope, wherein the above-mentioned Ming alloy powder is composed of si containing 0.4 to 2.0 weight ° / Q, Alloy powder formed from 0.4 to 2.0% by weight of Mg, 0.10 to 0.3% by weight of Fe, 0.05 to 0.6% by weight of Mn, and 0.05 to 0.6% by weight of Cr A1. In this case, the reason why the amount of Si added is 0.4 to 2.0% by weight is that the addition of Si will form a compound Mg2Si with Mg, and the minimum addition amount required to make the strength of the aluminum matrix after heat treatment is 300 MPa or more 0.4 200533763 (3) wt%, and if the amount of Si added exceeds 2.0 wt%, stretchability of more than 5% cannot be obtained, which causes problems in forging processing. In addition, the reason why the amount of Mg added is 0.4 to 2.0% by weight is that Mg needs to be added in order to form a compound Mg2Si that can improve the strength after heat treatment, and the minimum amount required to obtain a tensile strength of 300 MPa or more is 0. 4% by weight, and once Mg is added in an amount exceeding 2.0% by weight, the plastic workability will be reduced.

Fe將與Si形成Al_Fe-Si的化合物,而降低多餘的Si 導致延伸性下降的不良影響。Fe的添加量形成0.10〜0.3重 量%的原因爲:當添加量不滿0.10重量%時將使霧化粉末 的細微組織化效果消失,而一旦添加量超過0.3重量%將 導致拉伸性的下降。 Μη及Cr可藉由適量的添加,而具有抑制因熱加工導 致組織粗大化的效果。Μη及 Cr的添加量分別形成 0·05〜0.6重量%的原因爲··倘若添加量不滿〇.〇5重量%時 將不具上述效果,而一旦添加量超過0.6重量%將導致延 展性下降。 此外,氧化鋁的添加量形成1 0〜2 5重量% ,是爲了提 高彈性係數與耐磨耗性,這是由於一旦添加量不滿1 0重量 %時將導致彈性係數下降,而倘若超過25重量%時則導致 拉伸性下降之故。 申請專利範圍第3項所記載的發明,是申請專利範圍 第1或2項所記載的塑性加工用鋁合金,其中上述鋁合金粉 末的平均粒徑爲10〜150 // m,氧化鋁的平均粒徑爲5〜20 // 200533763Fe will form an Al_Fe-Si compound with Si, and the reduction of excess Si will lead to the adverse effect of reduced extensibility. The reason why Fe is added in an amount of 0.10 to 0.3% by weight is that when the added amount is less than 0.10% by weight, the microstructure effect of the atomized powder disappears, and if the added amount exceeds 0.3% by weight, the stretchability will decrease. The addition of Mn and Cr has the effect of suppressing the coarsening of the structure due to hot working by the addition of appropriate amounts. The reason why the addition amounts of Mn and Cr are 0.05 to 0.6% by weight is as follows. If the addition amount is less than 0.05% by weight, the above effect will not be obtained, and if the addition amount exceeds 0.6% by weight, the ductility will be reduced. In addition, the addition amount of alumina is 10 to 25% by weight to increase the elastic coefficient and abrasion resistance. This is because once the addition amount is less than 10% by weight, the elastic coefficient will decrease, and if it exceeds 25% by weight %% causes a decrease in stretchability. The invention described in item 3 of the patent application scope is an aluminum alloy for plastic working as described in item 1 or 2 of the patent application scope, wherein the average particle diameter of the aluminum alloy powder is 10 to 150 // m, and the average of the alumina is Particle size 5 ~ 20 // 200533763

在本發明中,鋁合金粉末的平均粒徑形成10〜150// m 的原因,是因爲一旦平均粒徑不滿10#m時將於鋁合金粉 末之間形成凝集,難以與氧化鋁形成平均的混合,導致增 加強度與拉伸性的參差不齊而對塑性加工性造成影響,而 倘若超過1 5 0 // m將使粗粒子的數量增加,而不易使氧化 鋁平均分散,導致增加強度與拉伸性的參差不齊而對塑性 加工性造成影響。 此外,氧化鋁的平均粒徑形成5〜20 μ m的原因,是爲 了提高彈性係數與耐磨耗性,這是由於一旦氧化鋁的平均 粒徑不滿5 // m將無法平均的混合,而一旦超過20 // m將 形成大量的粗大氧化鋁,而導致拉伸性及塑性加工性的下 降。 申請專利範圍第4項所記載的發明,是製造上述塑性 加工用鋁合金的製造方法,其特徵爲:在由0.4〜2.0重量 %的 Si、0.4〜2.0重量%的Mg ;和由含有從Fe、Mn、Cr 中選出一種以上合計〇· 5〜2 ·0重量% ,且剩餘部分含有無 法避免之不純物的A1所形成的鋁合金粉末中混合〇〜25重 量%的氧化鋁,並在室溫狀態下對該混合粉末加壓成形, 以200〜4 5 0°C對該成形體實施真空脫氣,並對以5 00〜600t: 之高溫燒結而成的成形體實施加壓燒結,在此之後實施鍛 造加工,而獲得室溫狀態下的彈性係數爲80GPa以上,水 淬處理後的室溫拉伸強度爲3 0 〇 Μ P a以上,且延展性爲5 % 以上,不會產生氣泡之成品的結構構件。 -8 - 200533763 (5) [發明的效果] 根據本發明,對自行車構件、釣具、高爾夫球桿及滑 雪板等高機能材料具有有用的局拉伸強度、高彈性係數, 相較於傳統構件即使氧化鋁的含有量爲1 〇重量%拉伸性也 未滿5 % ,在本發明中氧化鋁的含有量爲1 〇重量%以上拉 伸性可達8 % ,具有良好的延展性並適合塑性加工。此外 ,脫氣後也能抑制氣體的再吸收,而不會產生氣泡(蓬鬆) 之類的加工缺失,可獲得塑性加工用鋁合金。 【實施方式】 以下,針對本發明之塑性加工用鋁合金製造方法的最 佳實施形態,參考第1圖作詳細的說明。 首先,製作鋁合金急冷凝固粉末{步驟1-1,鋁合金粉 末製作過程},該鋁合金急冷凝固粉末是由含有:重量% ( 以下簡稱爲% )爲0.4〜2.0% (譬如0.8% )的 Si、0.4〜2.0% ( 譬如1 ·〇% )的Mg ;及含有從Fe、Mn、Cr中選出一種以上 合計 0.5 〜2.0% (譬如 Fe 爲 0.15% 、Μη 爲 0.05% 、Cr 爲 0.3 % ),剩餘部份含有不可避免之不純物的A1所形成。而 製作急冷凝固粉末的方法,利用業界所熟知的霧化法、熔 融紡絲法、迴轉圓盤法、迴轉電極法等製作方法即可,在 本發明中,是基於工業性生產的觀點採用霧化法(特別是 氣體霧化法)。此外,在製作該鋁合金粉末時,考慮到均 勻的混和、強度與延伸性的參差不齊,鋁合金粉末的平均 粒徑最好爲1〇〜150// m。其理由是因爲一旦鋁合金粉末的 -9- 200533763 (6) 平均粒徑未滿1 0 m,鋁合金粉末之間將發生凝集,而 以均勻地混合鋁合金粉末,此外,倘若鋁合金粉末的平 粒徑超過1 5 0 ν m將增加大量的粗大粒子,而難以使氧 鋁平均分散,導致強度與延伸性的參差不齊量大增,進 對塑性加工性造成不良的影響。 其次,利用直槽磨(pod mill )在上述的鋁合金急 凝固粉末中混入10〜25% (譬如IS% )之平均粒徑爲5〜 φ //m (譬如15//m)的氧化鋁(Ahoy後獲得的混合粉末 並對該混合粉末施以冷均壓成形(Cold Isostatic Pressi )後形成暫時成形{步驟1 - 2,加壓成形過程}。在本發 中’ AI2O3的平均粒徑爲5〜20//m,是由於一旦平均粒 未滿5 // m將無法均勻的混合,倘若超過20 // m將形成 量的粗大A1203,而導致延伸性及塑性加工性的低落。 接著,藉由真空吸引對暫時成形的混合粉末執行脫 處理{步驟1-3,脫氣處理過程}。由於一邊加熱一邊進 φ 脫氣處理將有助於氣體的去除,也能執行部分的燒結, 是以200〜45 (TC執行真空脫氣。一旦爐內溫度超過200t 可去除暫時成形體所吸收的氣體與水分,倘若爐內溫度 過300°C,將分解去除水合物(hydrate)。雖然這些現 也發生45 (TC以上的溫度,但一旦暫時成形體的溫度超 45 0 °C時將產生燒結,而促使去除空氣與水分後之暫時 形體內部的粉體間開始阻塞。因此,在本發明中,爲了 燒結開始之前執行充分的脫氣,是將成形體在爐內溫度 4〇〇°C的爐內保持1〜6小時(譬如1·5小時)。 難 均 化 而 冷 20 , ng 明 徑 大 氣 行 故 超 象 過 成 在 爲 -10- 200533763 (7) 接下來,進一步利用熱押出或熱壓延步驟,對以 5 0 0〜600它(譬如5 5 0它)的高溫保持1〜6小時(譬如4小時 )的燒結成形體進行加壓燒結{步驟1 -4 ’加壓燒結過程} 。在該加壓燒結過程中,一旦溫度未滿5 0 0 °C,覆蓋於粉 末表面的氧化物等將造成影響,由於燒結速度緩慢導致燒 結的進行遲緩,因此最好加熱至上述溫度(55 (TC )以上。 倘若形成上述溫度(5 5 0 °C )以上的溫度,粉末本身將軟 0 化而使部分表面熔融。熔融後所形成的熔液,將從覆蓋於 粉末表面之氧化物等的缺口滲出,並掩埋粉末之間的間隙 ,而促使燒結急速進行。此外,一旦保持於超過600 °C的 溫度將導致合金粉末產生熔融,而顯著降低熱加工材的機 械特性。倘若保持時間低於1小時,由於無法充分燒結, 因此保持時間必須爲1小時以上。相反地,一旦保持時間 超過6小時,將造成合金粉末中的結晶物-析出物粗大,而 導致熱加工材的機械特性低落。據此,保持時間最好爲 • 1〜6小時。 加壓燒結後,實施鍛造加工而獲得完成品的結構構件 {步驟1 - 5,鍛造加工過程}。 [實施例] 以下,針對經上述步驟所獲得知完成品的結構構件’ 也就是塑性加工用鋁合金之特性與表面觀察的實驗作說明 〇 首先,利用氣體霧化法製作含有表1所示之元素與 -11 - 200533763 (8)In the present invention, the reason why the average particle diameter of the aluminum alloy powder is 10 to 150 // m is because once the average particle diameter is less than 10 # m, aggregation will be formed between the aluminum alloy powders, and it is difficult to form an average with the alumina. Mixing results in uneven strength and stretchability and affects plastic workability. If it exceeds 1 5 0 // m, the number of coarse particles will increase, and it will not be easy to evenly disperse the alumina, resulting in increased strength and The uneven stretchability affects plastic workability. In addition, the reason why the average particle size of alumina is 5 to 20 μm is to improve the coefficient of elasticity and abrasion resistance. This is because once the average particle size of alumina is less than 5 // m, it cannot be mixed evenly, and Once it exceeds 20 // m, a large amount of coarse alumina will be formed, resulting in a decrease in stretchability and plastic workability. The invention described in item 4 of the scope of the patent application is a method for manufacturing the above-mentioned aluminum alloy for plastic working, which is characterized by comprising 0.4 to 2.0% by weight of Si and 0.4 to 2.0% by weight of Mg; and Mn, Cr, or more than one selected from a total of 0.5 ~ 2 · 0% by weight, and the remaining portion of the aluminum alloy powder formed by A1 containing unavoidable impurities is mixed with 0 ~ 25% by weight of alumina, and at room temperature The mixed powder is pressure-molded in a state, and the formed body is vacuum degassed at 200 to 450 ° C, and the molded body sintered at a high temperature of 500 to 600 t: is subjected to pressure sintering. Here, After forging, the elasticity coefficient at room temperature is 80 GPa or more, the room temperature tensile strength after water quenching is 300 MPa or more, and the ductility is 5% or more. Structural components of the finished product. -8-200533763 (5) [Effects of the invention] According to the present invention, it has useful local tensile strength and high elastic coefficient for high-performance materials such as bicycle components, fishing tackles, golf clubs, and snowboards. The content of aluminum is 10% by weight and the stretchability is less than 5%. In the present invention, the content of alumina is 10% by weight or more. The stretchability can reach 8%. It has good ductility and is suitable for plastic processing. . In addition, after degassing, it is possible to suppress the reabsorption of gas without generating processing defects such as bubbles (fluffy), and an aluminum alloy for plastic processing can be obtained. [Embodiment] Hereinafter, a preferred embodiment of a method for manufacturing an aluminum alloy for plastic working according to the present invention will be described in detail with reference to Fig. 1. First, an aluminum alloy rapid solidification powder is produced {step 1-1, aluminum alloy powder manufacturing process}. The aluminum alloy rapid solidification powder is composed of 0.4% to 2.0% (for example, 0.8%) by weight (hereinafter referred to as%). Si, 0.4 to 2.0% (e.g. 1.0%) Mg; and one or more selected from Fe, Mn, and Cr for a total of 0.5 to 2.0% (e.g., 0.15% Fe, 0.05% Mn, 0.3% Cr) , The remainder is formed by A1 containing unavoidable impurities. The method for producing the rapidly condensed solid powder may use the production methods such as the atomization method, the melt spinning method, the rotary disk method, and the rotary electrode method that are well known in the industry. In the present invention, the mist is used from the viewpoint of industrial production. Method (especially gas atomization method). In addition, when making this aluminum alloy powder, taking into account uniform mixing, variations in strength and elongation, the average particle diameter of the aluminum alloy powder is preferably 10 to 150 // m. The reason is that once the -9-200533763 (6) average particle diameter of the aluminum alloy powder is less than 10 m, aggregation will occur between the aluminum alloy powders to uniformly mix the aluminum alloy powders. In addition, if the aluminum alloy powders are The average particle size of more than 15 0 ν m will increase a large number of coarse particles, and it is difficult to evenly disperse the oxyaluminum, resulting in a large increase in the amount of unevenness in strength and ductility, which adversely affects plastic workability. Second, a straight groove mill (pod mill) is used to mix 10 ~ 25% (for example, IS%) average particle size of 5 ~ φ // m (for example, 15 // m) alumina into the above-mentioned aluminum alloy rapid solidification powder. (The mixed powder obtained after Ahoy was subjected to cold isostatic pressing (Cold Isostatic Pressi) to form temporary forming {steps 1-2, pressure forming process}. In this hair, the average particle diameter of AI2O3 is 5 ~ 20 // m is because once the average grain size is less than 5 // m, it will not be able to mix uniformly. If it exceeds 20 // m, the amount of coarse A1203 will be formed, resulting in a decrease in elongation and plastic workability. Next, Degassing the temporarily formed mixed powder by vacuum suction {steps 1-3, degassing treatment process}. As the φ degassing treatment while heating will help the gas removal, it can also perform partial sintering. Yes Vacuum degassing is performed at 200 ~ 45 ° C. Once the temperature in the furnace exceeds 200t, the gas and moisture absorbed by the temporarily formed body can be removed. If the temperature in the furnace exceeds 300 ° C, hydrates will be decomposed and removed. Temperatures above 45 (TC, but also temporarily When the temperature of the shape exceeds 45 0 ° C, sintering will occur, which will cause blockage between the powder inside the shape temporarily after the air and moisture are removed. Therefore, in the present invention, in order to perform sufficient degassing before the sintering starts, The shaped body is kept in a furnace at a temperature of 400 ° C for 1 to 6 hours (for example, 1.5 hours). It is difficult to homogenize and cold 20 ng. The superb appearance of the bright path is -10- 200533763. (7) Next, press the sintered compact at a high temperature of 500 to 600 (for example, 5 to 50) for 1 to 6 hours (for example, 4 hours) by using a hot extrusion or hot rolling step. Sintering {Step 1-4 'Pressure sintering process}. In this pressure sintering process, once the temperature is less than 50 ° C, oxides and the like covering the surface of the powder will affect the sintering due to the slow sintering speed. It is delayed, so it is best to heat it to the above temperature (55 (TC) or higher. If the temperature is higher than the above temperature (550 ° C), the powder itself will be softened to melt part of the surface. Liquid that will cover the powder from the table Notches such as oxides ooze out and bury the gaps between the powders, which promotes rapid sintering. In addition, once the temperature is maintained above 600 ° C, the alloy powder will melt, which will significantly reduce the mechanical properties of the hot-worked material. If the holding time is less than 1 hour, it cannot be fully sintered, so the holding time must be more than 1 hour. Conversely, once the holding time exceeds 6 hours, the crystals and precipitates in the alloy powder will be coarse, which will cause hot working materials. The mechanical properties are low. Based on this, the holding time is preferably 1 to 6 hours. After pressure sintering, forging processing is performed to obtain a finished structural member {steps 1-5, forging processing process}. [Examples] Hereinafter, the structural members of the known finished product obtained through the above steps, that is, the experiments of the characteristics and surface observation of aluminum alloys for plastic working will be described. First, the gas atomization method containing Elements with -11-200533763 (8)

Al2〇3的鋁合金急冷凝固粉末。利用冷均壓成形將所獲得 的鋁合金粉末成形爲直徑3 2 5 mm的小九體。以3 8 0 °C的溫 度將所獲得的小九體在真空爐內保持1小時,執行脫氣處 理,稍後令經5 60°C高溫(表1中的Νο·22與^^〇.23爲480它 )燒結2小時所得的成形體冷卻至常溫後,利用誘導加熱 的方式加熱至5 00 °C ,押出加壓成圓棒,實施水淬處理 (T6),也就是以540 °C保持2小時後施以水冷,以執 行6小時的人工時效處理後,獲得如表2所示的,結果。Al2O3 aluminum alloy rapidly condenses and solidifies powder. The obtained aluminum alloy powder was formed into a small nine-body body having a diameter of 3 2 5 mm by cold equalizing forming. The obtained small nine body was maintained in a vacuum furnace at a temperature of 3 80 ° C for 1 hour, and a degassing treatment was performed, and then subjected to a high temperature of 5 60 ° C (No. 22 and ^^ 〇 in Table 1). It is 23 for 480) After sintering for 2 hours, the formed body is cooled to normal temperature, and then heated to 500 ° C by induction heating, extruded and pressed into a round rod, and subjected to water quenching treatment (T6), that is, 540 ° C. After holding for 2 hours, water cooling was applied to perform artificial aging treatment for 6 hours, and the results are shown in Table 2.

-12- 200533763 (9) 表1-12- 200533763 (9) Table 1

(單位:重量% ) 銘合金粉末 Al2〇3 燒結溫 度。c NO Si Mg Fe Μη Cr A1 平均粒徑 μ m ai2o3 平均粒 徑// m 發 1 2.0 0.4 0.3 0.6 0.6 殘 150 25 20 560 明 2 1.0 2.0 0.2 0.3 0.05 殘 80 15 10 560 合 3 0.4 1.5 0.1 0.05 0.3 殘 10 10 5 560 金 4 0.8 1.0 0.15 0.05 0.3 殘 100 15 15 560 5 1.0 1.0 0.2 0.5 0.5 殘 80 30 10 560 6 1.0 1.0 0.2 0.5 0.5 殘 80 5 10 560 7 1.0 1.0 0.2 0.5 0.5 殘 80 20 25 560 8 1.0 1.0 0.2 0.5 0.5 殘 200 20 10 560 9 1.0 1.0 0.2 0.5 0.5 殘 5 20 10 560 10 0.2 1.5 0.2 0.5 0.5 殘 80 20 10 560 11 1.5 0.2 0.2 0.5 0.5 殘 80 20 10 560 對 比 合 金 12 1.0 1.0 0.05 0.5 0.5 殘 80 20 10 560 13 1.0 1.0 0.2 0.04 0.5 殘 80 20 10 560 14 1.0 1.0 0.2 0.5 0.04 殘 80 20 10 560 15 2.5 1.0 0.2 0.5 0.5 殘 80 20 10 560 16 1.0 2.5 0.2 0.5 0.5 殘 80 20 10 560 17 1.0 1.0 0.4 0.5 0.5 殘 80 20 10 560 18 1.0 1.0 0.2 0.8 0.5 殘 80 20 10 560 19 1.0 1.0 0.2 0.5 0.8 殘 80 20 10 560 20 0.2 0.2 0.2 0.5 0.5 殘 80 20 10 560 21 2.5 2.5 0.2 0.5 0.5 殘 80 20 10 560 22 1.0 1.0 0.5 0.8 0.8 殘 80 20 10 480 23 1.0 2.0 0.2 0.3 0.3 殘 80 10 10 480 •13- 200533763(10)(Unit:% by weight) Ming alloy powder Al2O3 sintering temperature. c NO Si Mg Fe Mn Cr A1 average particle size μ m ai2o3 average particle size // m hair 1 2.0 0.4 0.3 0.6 0.6 residual 150 25 20 560 Ming 2 1.0 2.0 0.2 0.3 0.05 residual 80 15 10 560 in 3 0.4 1.5 0.1 0.05 0.3 residual 10 10 5 560 gold 4 0.8 1.0 0.15 0.05 0.3 residual 100 15 15 560 5 1.0 1.0 0.2 0.5 0.5 residual 80 30 10 560 6 1.0 1.0 0.2 0.5 0.5 residual 80 5 10 560 7 1.0 1.0 0.2 0.5 0.5 residual 80 20 25 560 8 1.0 1.0 0.2 0.5 0.5 residual 200 20 10 560 9 1.0 1.0 0.2 0.5 0.5 residual 5 20 10 560 10 0.2 1.5 0.2 0.5 0.5 residual 80 20 10 10 560 11 1.5 0.2 0.2 0.5 0.5 residual 80 20 10 560 contrast alloy 12 1.0 1.0 0.05 0.5 0.5 residual 80 20 10 560 13 1.0 1.0 0.2 0.04 0.5 residual 80 20 10 10 560 14 1.0 1.0 0.2 0.5 0.04 residual 80 20 10 560 15 2.5 1.0 0.2 0.5 0.5 residual 80 20 10 560 16 1.0 2.5 0.2 0.5 0.5 residual 80 20 10 560 17 1.0 1.0 0.4 0.5 0.5 residual 80 20 10 560 18 1.0 1.0 0.2 0.8 0.5 residual 80 20 10 560 19 1.0 1.0 0.2 0.5 0.8 residual 80 20 10 560 20 0.2 0.2 0.2 0.5 0.5 residual 80 20 10 560 21 2.5 2.5 0.2 0.5 0.5 residual 80 20 10 560 22 1.0 1.0 0.5 0.8 0.8 residual 80 20 10 480 23 1.0 2.0 0.2 0.3 0.3 Residual 80 10 10 480 • 13- 200533763 (10)

表2Table 2

NO 拉伸強度(MPa) 延伸性(% ) 彈性係數(GPa) 是否有氣泡 發明 ί=ι 36: 1 305 6.8 85 〇 2 350 5.2 87 〇 3 320 7.5 80 〇 4 367 8.5 86.5 〇 對比 合金 5 340 1.8 88 〇 6 335 5.2 75 〜86 〇 7 350 3.4 82 〇 8 330 2.5 79 〇 9 290〜340 3〜5 74 〜82 〇 10 280 4.2 82 〇 11 250 4.6 78 〇 12 290 4.0 82 〇 13 305 4.8 82 〇 14 320 4.7 8 1 〇 15 335 2.8 84 〇 16 340 3.2 80 〇 17 3 10 3.5 80 〇 18 325 2.8 83 〇 19 330 3.6 83 〇 20 240 4.5 75 〇 2 1 350 2.2 82 〇 22 280 3.9 76 〇 23 290 4.8 75 X 「是否有氣泡」一欄中,「〇」表示完全沒有氣泡, 「X」表示產生氣泡。 氧化鋁粒徑、鋁合金粉末粒徑較小時(No.6、No.9 ), 將加大參差不齊的現象,導致平均的特性値下降。 -14- 200533763 (11) 上述的實驗結果,本發明合金(No. 1〜No ·4 )的拉伸 強度爲3 0 5〜3 67MPa,彈性係數爲80〜87GPa,延伸性爲 5.2〜8.5% ,顯示出充分的高拉伸強度、彈性係數及延伸 性。此外,於脫氣後也能抑制氣體的再吸附,可獲得不會 產生氣泡等加工缺失的塑性加工用鋁合金。相對於此,對 比合金(Νο·5〜No.23 ),由於鋁合金粉末和A1203的成分 量和平均粒徑及燒結溫度並不適當,因此被判定拉伸強度 φ 、彈性係數及延伸性不足,參差不齊現象大增且產生氣泡 〇 據此,藉由在由:0.4〜2.0重量%的Si、0·4〜2.0重量 %的Mg;和由含有從Fe、Mn、Cr中選出一種以上合計 〇.5〜2.0重量% ,且剩餘部分含有無法避免之不純物的A1 所形成的鋁合金粉末中,分散1〇〜25重量!ίί的氧化鋁,可 獲得室溫狀態下的彈性係數爲80GPa以上,水淬處理後的 室溫拉伸強度爲3 00MPa以上,且延展性爲5%以上的塑性 φ 加工用鋁合金。 【圖式簡單說明】 第1圖:顯示本發明之塑性加工用鋁合金之製造方法 的步驟流程圖。 -15-NO Tensile strength (MPa) Elongation (%) Elastic coefficient (GPa) Whether there is a bubble invention ί = ι 36: 1 305 6.8 85 〇2 350 5.2 87 〇3 320 7.5 80 〇4 367 8.5 86.5 〇Compare alloy 5 340 1.8 88 〇6 335 5.2 75 to 86 〇7 350 3.4 82 〇8 330 2.5 79 〇9 290 to 340 3 to 5 74 to 82 〇10 280 4.2 82 〇11 250 4.6 78 〇12 290 4.0 82 〇13 305 4.8 82 〇14 320 4.7 8 1 〇15 335 2.8 84 〇16 340 3.2 80 〇17 3 10 3.5 80 〇18 325 2.8 83 〇19 330 3.6 83 〇20 240 4.5 75 〇2 1 350 2.2 82 〇22 280 3.9 76 〇23 290 4.8 75 X In the "Are there any bubbles" column, "0" means that there are no bubbles at all, and "X" means that bubbles are generated. When the particle size of alumina and aluminum alloy powder is small (No.6, No.9), the phenomenon of unevenness will increase, and the average characteristic will decrease. -14- 200533763 (11) According to the above experimental results, the tensile strength of the alloy (No. 1 to No. 4) of the present invention is 3 0 5 to 3 67 MPa, the elastic coefficient is 80 to 87 GPa, and the elongation is 5.2 to 8.5%. , Showing sufficient high tensile strength, modulus of elasticity and elongation. In addition, it is possible to suppress re-adsorption of the gas after degassing, and to obtain an aluminum alloy for plastic working without loss of processing such as generation of bubbles. On the other hand, the comparative alloy (Nο · 5 ~ No.23) was judged to have insufficient tensile strength φ, elastic coefficient, and elongation because the component amounts, average particle diameters, and sintering temperatures of aluminum alloy powder and A1203 were not appropriate. The uneven phenomenon greatly increased and bubbles were generated. Based on this, by: 0.4 to 2.0% by weight of Si, 0.4 to 2.0% by weight of Mg; and one or more selected from the group consisting of Fe, Mn, and Cr A total of 0.5 to 2.0% by weight, and the remainder of the aluminum alloy powder formed by A1 containing unavoidable impurities is dispersed by 10 to 25% by weight! The alumina can obtain a plastic φ aluminum alloy for processing at room temperature with an elastic coefficient of 80 GPa or more, a room temperature tensile strength of 300 MPa or more, and a ductility of 5% or more after water quenching. [Brief description of the drawings] Fig. 1: A flowchart showing the steps of a method for manufacturing an aluminum alloy for plastic working according to the present invention. -15-

Claims (1)

200533763 (1) 十、申請專利範圍 1. 一種塑性加工用鋁合金,其特徵爲:是由·· 0.4〜2.0 重量%的Si、0.4〜2.0重量%的Mg ;和由含有從Fe、Μη 、Cr中選出一種以上合計0.5〜2.0重量% ,且剩餘部分含 有無法避免之不純物的A1所形成的鋁合金粉末;及10〜2 5 重量%的氧化鋁所混合而成的固化成形材,室溫狀態下的 彈性係數爲80GPa以上,水洋處理(water quenching)後 的室溫拉伸強度爲3 00 MPa以上,且延展性爲5%以上。 2 ·如申請專利範圍第1項所記載的塑性加工用鋁合金 ,其中上述的鋁合金粉末,是由含有·· 0.4〜2.0重量%的 S i、0 · 4〜2 · 0重量% 的 M g、0 · 1 0〜〇 · 3重量% 的 Fe、 0.05〜0.6重量%的Mn、0.05〜0.6重量%之Cr的A1所形成 的合金粉末。 3 ·如申請專利範圍第1或2項所記載的塑性加工用鋁合 金,其中上述鋁合金粉末的平均粒徑爲10〜15 Ομπι,氧化 鋁的平均粒徑爲5〜20μιη。 4 · 一種塑性加工用銘合金的製造方法,是在由〇 . 4〜2 · 0 重量%的S i、0 · 4〜2 · 0重量%的M g ;和由含有從f e、Μ η、 Cr中選出一種以上合計0.5〜2.0重量% ,且剩餘部分含有 無法避免之不純物的A1所形成的鋁合金粉末中混合10〜2 5 重量%的氧化鋁,並在室溫狀態下對該混合粉末加壓成形 ,以200〜450°C對該成形體實施真空脫氣,並對以 5 0 0〜6 0 0 °C之高溫燒結而成的成形體實施加壓燒結,在此 之後實施鍛造加工,而獲得室溫狀態下的彈性係數爲 -16- 200533763 (2) 80GPa以上,水淬處理後的室溫拉伸強度爲3 00MPa以上, 且延展性爲5 %以上,不會產生氣泡之成品的結構構件。200533763 (1) X. Application for patent scope 1. An aluminum alloy for plastic processing, characterized by: 0.4 to 2.0% by weight of Si, 0.4 to 2.0% by weight of Mg; and containing from Fe, Mη, Cr is selected from the group consisting of more than 0.5 to 2.0% by weight of A1, and the remainder contains unavoidable impurities of A1, which is an aluminum alloy powder; and 10 to 25% by weight of alumina, a solidified molding material mixed at room temperature The elastic coefficient in the state is 80 GPa or more, the room-temperature tensile strength after water quenching is 300 MPa or more, and the ductility is 5% or more. 2 · The aluminum alloy for plastic working as described in item 1 of the patent application range, wherein the aluminum alloy powder is composed of 0.4 to 2.0% by weight of Si, 0 to 4 to 2 and 0% by weight of M. g, an alloy powder formed of 0. 10 to 0.3% by weight of Fe, 0.05 to 0.6% by weight of Mn, and 0.05 to 0.6% by weight of Cr A1. 3. The aluminum alloy for plastic working as described in item 1 or 2 of the scope of patent application, wherein the average particle diameter of the aluminum alloy powder is 10 to 15 μm, and the average particle diameter of the aluminum oxide is 5 to 20 μm. 4 · A method for manufacturing a sintered alloy for plastic working, which is composed of 0.4 to 2% by weight of Si and 0.4 to 2% by weight of Mg; and One or more Cr is selected from a total of 0.5 to 2.0% by weight, and the remaining portion contains aluminum alloy powder formed by A1 containing unavoidable impurities. 10 to 25% by weight of alumina is mixed with the mixed powder at room temperature. Press forming, vacuum degassing the formed body at 200 to 450 ° C, and press sintering the formed body sintered at a high temperature of 500 to 600 ° C, and then forging , And obtain the elastic coefficient at room temperature of -16-200533763 (2) 80GPa or more, the room temperature tensile strength after water quenching is 300 MPa or more, and the ductility is 5% or more, without bubbles Structural components. -17--17-
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