JPH0327620B2 - - Google Patents
Info
- Publication number
- JPH0327620B2 JPH0327620B2 JP2367987A JP2367987A JPH0327620B2 JP H0327620 B2 JPH0327620 B2 JP H0327620B2 JP 2367987 A JP2367987 A JP 2367987A JP 2367987 A JP2367987 A JP 2367987A JP H0327620 B2 JPH0327620 B2 JP H0327620B2
- Authority
- JP
- Japan
- Prior art keywords
- cold working
- alloy
- less
- rate
- damping capacity
- 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.)
- Expired
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- 229910045601 alloy Inorganic materials 0.000 claims description 38
- 239000000956 alloy Substances 0.000 claims description 38
- 238000013016 damping Methods 0.000 claims description 33
- 238000005482 strain hardening Methods 0.000 claims description 29
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 19
- 238000010438 heat treatment Methods 0.000 claims description 14
- 229910052782 aluminium Inorganic materials 0.000 claims description 9
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 9
- 238000002844 melting Methods 0.000 claims description 7
- 230000008018 melting Effects 0.000 claims description 7
- 229910018507 Al—Ni Inorganic materials 0.000 claims description 6
- 229910052759 nickel Inorganic materials 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 229910004261 CaF 2 Inorganic materials 0.000 claims description 2
- 229910021538 borax Inorganic materials 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 230000004907 flux Effects 0.000 claims description 2
- 239000004328 sodium tetraborate Substances 0.000 claims description 2
- 235000010339 sodium tetraborate Nutrition 0.000 claims description 2
- 238000010583 slow cooling Methods 0.000 claims 3
- 238000001816 cooling Methods 0.000 claims 1
- 238000004090 dissolution Methods 0.000 claims 1
- 238000000034 method Methods 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 230000007423 decrease Effects 0.000 description 5
- 239000012456 homogeneous solution Substances 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 238000000137 annealing Methods 0.000 description 3
- 230000005484 gravity Effects 0.000 description 3
- 238000004080 punching Methods 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- KHYBPSFKEHXSLX-UHFFFAOYSA-N iminotitanium Chemical compound [Ti]=N KHYBPSFKEHXSLX-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 229910001000 nickel titanium Inorganic materials 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 229910018182 Al—Cu Inorganic materials 0.000 description 1
- 229910000881 Cu alloy Inorganic materials 0.000 description 1
- 229910000990 Ni alloy Inorganic materials 0.000 description 1
- 239000011358 absorbing material Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 229910002056 binary alloy Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000002981 blocking agent Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 230000005294 ferromagnetic effect Effects 0.000 description 1
- 238000005242 forging Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000009931 harmful effect Effects 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 230000005291 magnetic effect Effects 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M potassium chloride Inorganic materials [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 1
- 238000003303 reheating Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
Landscapes
- Powder Metallurgy (AREA)
- Hard Magnetic Materials (AREA)
Description
本発明は各種の交通機関、大型機械の振動およ
び騒音による公害、各種精密機械、電子機器の振
動による性能劣化または生活環境に存在する種々
な振動や騒音の害を防止するのに最適な振動減衰
能の大きなAl−Ni吸振合金に関するものである。
一般に減衰能力を比較するために用いる減衰能
Q-1は振動のサイクル中に失われる振動エネルギ
ーΔEおよび全振動エネルギーEと次式のような
関係にある。
Q-1=1/2π・ΔE/E
つまりQ-1の値が大きいほど短時間で振幅が小
さくなつて減衰効果が大きいことになる。
従来知られている吸振合金としては、ジエンタ
ロイなどのFe基合金やMn−Cu系合金、Al−Cu
−Ni系合金およびNi−Ti系合金などがある。ジ
エンタロイなどのFe基吸振合金およびMn−Cu系
合金は減衰能は大きいが、比重が8g/cm3前後で
大きく、機器の軽量化を条件とする場合には不適
当で、またAl−Cu−Ni系合金およびNi−Ti系合
金は冷間加工性が悪く、冷間加工が全く不可能で
あるという欠点を有する。
本発明は従来の吸振合金に比較して軽量な吸振
合金を得るために比重が2.7g/cm3で非常に小さ
いアルミニウムを基としてこれに重量比で0.1〜
20%のニツケルを加えた合金に融点以下250℃以
上の温度で均質固溶化熱処理を施した後、冷間加
工率5%以上の加工を施して転位を増加させ、必
要に応じて250℃以下の温度で熱処理し、その履
歴現象によつて大きな減衰能をもたせると同時に
高い強度をもつ吸振合金を提供することにある。
次に本発明合金の製造方法について説明する。
まず上記の組成範囲の合金を空気中もしくは不
活性ガス中または真空中において通常の溶解炉に
よつて溶解した後十分に撹拌して均一な溶湯と
し、砂型や金型などに鋳込んで鋳塊を造る。
次にこの鋳塊に次のごとき熱処理を施す。
(A) 均質溶体化処理のためなるべく高温において
例えばその合金の融点以下250℃以上の温度で
5分間以上100時間以下(好ましくは30分間以
上)加熱した後、急冷するかあるいは毎秒1℃
以下の速度で徐冷する。
(B) つづいて常温において鍛造、圧延、押出、ス
エージングあるいは引き抜きなどによつて本発
明の目的とする大きな減衰能を得るために冷間
加工率5%以上の冷間加工を施す。
(C) (B)の冷間加工率5%以上の加工を施したもの
を250℃以下の温度で1分間以上(好ましくは
30分以上500時間以下)加熱して急冷するか毎
秒1℃以下の速度で徐冷する。
なお、溶解する際には遮断剤としてMgCl2、硼
砂、CaF2、KClなどの全量5%以下のフラツク
スを添加し、脱酸剤としてMg、Beなどの全量
0.5%以下を加えてもよい。
工程(A)において均質溶体化処理するのは溶湯の
凝固の際の鋳塊各部の温度差や固液両相の比較差
に基づいて鋳塊に成分の不均質が起るときがある
から、その成分を均質にするためである。そして
加熱温度が高ければ加熱時間を短くすることがで
き、加熱温度が低ければ加熱時間を長くしなけれ
ばならない。一方、成形体の重量が大きければ、
加熱温度を上げ、加熱時間を長くする必要がある
が、成形体の重量が小さければ比較的低温で短時
間加熱してもよい。この理由は、溶体化処理を十
分に行わなければ、減衰能などの製品の性能を均
一にすることができないからである。
溶体化処理工程(A)続いて(B)工程の冷間加工をす
るのは加工歪によつて転位密度を増大させ、その
履歴現象によつて大きな減衰能を得るために必須
な工程であり、また該成形体の引張強度を高める
ためにも必要である。なお減衰能を大きくするた
めには、5%以上の冷間加工を施すだけで充分そ
の目的が達せられるが、冷間加工率が70〜95%如
く大きい場合及びNi量を多く加えた合金によつ
ては曲げ、深絞り、打抜きなどの成形が困難なも
のがある。このために、工程(B)において冷間加工
後ものを次の工程(C)で250℃以下の温度に加熱す
ると、減衰能および強度が格別低下せず常温にお
いて曲げ、深絞り、打ち抜きなどの成形加工が容
易になる。この場合の加熱温度を250℃以上とす
ると伸びは24%以上に急激に増加するが、減衰能
Q-1が4×10-3以下に低下するので好ましくな
い。
次に本発明の実施例について説明する。
実施例
第1表に示す組成の金属の全量100gをアルミ
ナ坩堝中で表面にアルゴンガスを通じながら高周
波誘導電気炉により溶解し、鉄型に鋳込んで直径
10mmの鋳塊を得た。次にこれを500℃で5時間加
熱して徐冷した後、冷間スエージングおよび引抜
きによつて1.1mmの線にし、これから長さ150mmの
線を切りとつて試料とした。減衰能Q-1の測定は
逆吊り捩れ振子法により振動数約1Hz、最大歪み
振幅γn=10×10-6で行なつた。
Al基合金の減衰能Q-1ならびに引張強度は冷間
加工率に依存する。第1図および第2図にはその
一例としてAl−50%Ni合金を500℃で5時間加熱
後、徐冷して冷間スエージングおよび引抜きによ
つて加工したときの減衰能Q-1および引張強度σt
と冷間加工率との関係がそれぞれ示してある。減
衰能Q-1および引張強度σtはいずれも冷間加工率
の増加とともに大きくなつており、これは加工歪
みの増加とともに転位密度が増大した結果であ
る。これによつて本発明の目的とする減衰能Q-1
=6×10-3以上(γn=10×10-6)を得るには5%
以上の冷間加工を施す必要があることがわかる。
次にAl−Ni二元合金について冷間加工率と減
衰能Q-1の関係を示すと第1表のとおりである。
The present invention provides vibration damping that is ideal for preventing pollution caused by vibration and noise from various transportation systems and large machinery, performance deterioration caused by vibration from various precision machines and electronic equipment, and the harmful effects of various vibrations and noises that exist in the living environment. This paper concerns an Al-Ni vibration absorbing alloy with high performance. Attenuation capacity generally used to compare attenuation capacity
Q -1 has a relationship with the vibrational energy ΔE lost during the vibration cycle and the total vibrational energy E as shown in the following equation. Q -1 = 1/2π·ΔE/E In other words, the larger the value of Q -1 , the smaller the amplitude becomes in a shorter time and the greater the damping effect. Conventionally known vibration absorbing alloys include Fe-based alloys such as dientalloy, Mn-Cu alloys, and Al-Cu alloys.
-Ni-based alloys and Ni-Ti-based alloys. Fe-based vibration-absorbing alloys such as dientalloy and Mn-Cu-based alloys have a large damping capacity, but their specific gravity is around 8 g/ cm3 , making them unsuitable when reducing the weight of equipment. Ni-based alloys and Ni-Ti-based alloys have a drawback in that they have poor cold workability and are completely impossible to cold work. In order to obtain a vibration-absorbing alloy that is lighter than conventional vibration-absorbing alloys, the present invention is based on aluminum, which has a very small specific gravity of 2.7 g/ cm3 , and has a weight ratio of 0.1 to
After applying homogeneous solution heat treatment to an alloy containing 20% nickel at a temperature below the melting point of 250°C or higher, cold working is performed at a rate of 5% or higher to increase dislocations, and if necessary, the temperature is reduced to 250°C or lower. The object of the present invention is to provide a vibration-absorbing alloy which is heat-treated at a temperature of 100 to 100 mm and has a large damping capacity due to the hysteresis phenomenon and at the same time has high strength. Next, a method for manufacturing the alloy of the present invention will be explained. First, an alloy with the above composition range is melted in an ordinary melting furnace in air, an inert gas, or a vacuum, and then sufficiently stirred to form a uniform molten metal.Then, the alloy is poured into a sand mold or metal mold, and an ingot is poured into an ingot. Build. Next, this ingot is subjected to the following heat treatment. (A) For homogeneous solution treatment, heat at a temperature as high as possible, e.g., below the melting point of the alloy, at a temperature of 250°C or higher, for 5 minutes to 100 hours (preferably 30 minutes or more), and then rapidly cool it or heat it at 1°C per second.
Cool slowly at the following speed. (B) Subsequently, cold working is performed at room temperature by forging, rolling, extrusion, swaging, or drawing at a cold working rate of 5% or more in order to obtain the large damping capacity that is the objective of the present invention. (C) A product that has been processed with a cold working ratio of 5% or more in (B) at a temperature of 250℃ or less for 1 minute or more (preferably
(30 minutes to 500 hours) and then rapidly cooled, or slowly cooled at a rate of 1°C per second or less. In addition, when dissolving, a flux of 5% or less of the total amount of MgCl 2 , borax, CaF 2 , KCl, etc. is added as a blocking agent, and a total amount of Mg, Be, etc. is added as a deoxidizing agent.
0.5% or less may be added. The reason why homogeneous solution treatment is carried out in step (A) is because the inhomogeneity of components may occur in the ingot due to the temperature difference in each part of the ingot during solidification of the molten metal and the comparative difference between the solid and liquid phases. This is to make the ingredients homogeneous. If the heating temperature is high, the heating time can be shortened, and if the heating temperature is low, the heating time must be lengthened. On the other hand, if the weight of the molded object is large,
Although it is necessary to raise the heating temperature and lengthen the heating time, if the weight of the molded product is small, it may be heated at a relatively low temperature for a short time. The reason for this is that unless the solution treatment is sufficiently performed, the performance of the product, such as the damping capacity, cannot be made uniform. The solution treatment process (A) followed by the cold working process (B) is an essential process in order to increase the dislocation density due to processing strain and obtain a large damping capacity due to the hysteresis phenomenon. , is also necessary to increase the tensile strength of the molded article. In order to increase the damping capacity, cold working of 5% or more is enough to achieve the objective, but when the cold working rate is as high as 70 to 95% or when alloys with a large amount of Ni are added. Some materials are difficult to form by bending, deep drawing, punching, etc. For this reason, if the product after cold working in step (B) is heated to a temperature of 250℃ or less in the next step (C), the damping capacity and strength will not deteriorate significantly and it can be bent, deep drawn, punched, etc. at room temperature. Molding becomes easier. In this case, when the heating temperature is set to 250℃ or higher, the elongation increases rapidly to 24% or higher, but the damping capacity
This is not preferable because Q -1 decreases to 4×10 -3 or less. Next, examples of the present invention will be described. Example A total of 100 g of metal having the composition shown in Table 1 was melted in an alumina crucible in a high-frequency induction electric furnace while passing argon gas to the surface, and cast into an iron mold.
A 10 mm ingot was obtained. Next, this was heated at 500° C. for 5 hours and slowly cooled, then cold swaged and drawn into a 1.1 mm wire, and a 150 mm long wire was cut from this to serve as a sample. The damping capacity Q -1 was measured by the inverted torsion pendulum method at a frequency of about 1 Hz and a maximum strain amplitude γ n =10×10 -6 . The damping capacity Q -1 and tensile strength of Al-based alloys depend on the cold working rate. As an example, Figures 1 and 2 show the damping capacity Q -1 and Tensile strength σ t
The relationship between and the cold working rate is shown respectively. Both the damping capacity Q -1 and the tensile strength σ t increase with increasing cold working rate, which is a result of the dislocation density increasing with increasing working strain. By this, the attenuation capacity Q -1 which is the object of the present invention
= 5% to obtain 6×10 -3 or more (γ n =10×10 -6 )
It can be seen that it is necessary to perform the above cold working. Next, Table 1 shows the relationship between cold working rate and damping capacity Q -1 for Al-Ni binary alloys.
【表】
第1表から明らかなように冷間加工率95%を施
したアルミニウムは減衰能Q-1が4×10-3で本発
明の目的とする吸振材料として不適当であるが、
アルミニウムに0.1%以上のニツケルを添加する
と本発明の目的とするQ-1=6×10-3以上の大き
い値が得られることがわかる。
要するに本発明合金の減衰能Q-1の値は一般の
金属の減衰能Q-1=1×10-3程度の値に比較して
数十倍大きい。
以上のように本発明においては、冷間加工率は
5%以上95%迄大きい程減衰能は高くなるが、伸
びが小さくなり脆く加工性が減少するので、250
℃以下の温度で焼鈍する必要がある。250℃以下
の温度で焼鈍すると伸びが大きくなり加工し易く
なり減衰能が若干落ちるが支障ない。これは加工
により転位を増加させたものが、焼鈍によりなま
され、転位が少なくなるからである。なお、焼鈍
温度を250℃にあげると伸びは25%以上に急激に
増大するが、減衰能Q-1が4×10-3以下となり本
発明の目的とするものが得られない。
さらに本発明合金の比重ρも一般の金属の7〜
9g/cm3に比べてかなり小さく、引張強度σtは冷
間加工したアルミニウムの10Kg/mm2に比較してか
なり大きい。例えば実施例の試料No.1はσt=19
Kg/mm2、ρ=2.8g/cm3を示している。
最後に本発明合金の組成を限定した理由につい
て述べる。まず本発明のAl−Ni吸振合金におい
てNiは減衰能Q-1の向上に寄与するばかりでな
く、合金を強化する。Niを重量比で0.1〜20%と
限定したのは組成の下限に満たないときには本発
明の目的とする十分な減衰能が得られないし、上
記の組成の上限を越えるときには減衰能が悪くな
り、また冷間加工が不可能となるからである。
なお、均質溶体化処理のために250℃以上融点
以下の温度で100時間以下の長時間加熱し、充分
な均質溶体化処理をすることは所要とする減衰
能、強度および加工性を得るために絶対必要であ
る。
なお、ここで冷間加工率5%以上の冷間加工を
施すことは加工歪み、転位密度を増大させること
により減衰能を増大させることに絶対必要な条件
である。
合金の成形体をアルミニウムの融点以下250℃
以上の高温で長時間加熱により均質固溶化処理を
すると、アルミのマトリツクス中のNi粒子の分
散の状態が均質となる。これに冷間加工率5%以
上の冷間加工を施すと、Ni粒子が微細に分散し、
転位密度が大となる。この転位密度が大きくなる
と、外部より振動が加えられたときに、加えられ
た外力(振動、衝撃、捩り、圧縮、引張り等)は
熱エネルギーその他となつて消滅するために振動
の減衰が生ずるのである。
従つて、減衰能を大きくするためには、250℃
以上の高温における長時間加熱と5%以上の冷間
加工を施すことだけで充分その目的が達せられる
が、冷間加工率を70%〜95%の如く高めた場合お
よびNiを多く加えた合金の組成によつては曲げ、
深絞り、打ち抜きなどの成形が困難なものがあ
る。このために、250℃以下の低温で長時間再加
熱処理をすると、減衰能および強度が格別低下せ
ず曲げ、深絞り、打ち抜きなどの成形加工が極め
て容易となるのである。この場合の再加熱処理は
250℃以上とすると減衰能が低下するので好まし
くない。
本発明合金の特徴は上述のように減衰能が大き
いこと、軽量であること、冷間加工性が良好で強
度が高い上に非強磁性であることである。従つて
本発明合成は各種の交通機関、自動車用内燃機
関、大型機械、電子機器の可動部、磁界で作動す
る部品、各種家庭用品ならびに建築などの構造材
料に応用し、振動および騒音の防止、軽量化を計
るのに非常に適している。[Table] As is clear from Table 1, aluminum subjected to 95% cold working has a damping capacity Q -1 of 4 x 10 -3 , making it unsuitable as a vibration absorbing material for the purpose of the present invention.
It can be seen that when 0.1% or more of nickel is added to aluminum, a large value of Q −1 =6×10 −3 or more, which is the object of the present invention, can be obtained. In short, the value of the damping capacity Q -1 of the alloy of the present invention is several tens of times larger than the value of the damping capacity Q -1 =1×10 -3 of general metals. As described above, in the present invention, as the cold working rate increases from 5% to 95%, the damping capacity increases, but the elongation decreases and the workability decreases due to brittleness.
It is necessary to anneal at a temperature below ℃. When annealing at a temperature below 250℃, the elongation increases, making it easier to process, and the damping capacity decreases slightly, but this is not a problem. This is because the number of dislocations increased by processing is annealed by annealing, resulting in fewer dislocations. In addition, when the annealing temperature is raised to 250°C, the elongation increases rapidly to 25% or more, but the damping capacity Q -1 becomes 4 x 10 -3 or less, and the object of the present invention cannot be obtained. Furthermore, the specific gravity ρ of the alloy of the present invention is 7 to 7 of that of general metals.
The tensile strength σ t is considerably smaller than 9 g/cm 3 , and the tensile strength σ t is considerably higher than 10 Kg/mm 2 for cold-worked aluminum. For example, sample No. 1 of the example has σ t =19
Kg/mm 2 , ρ=2.8g/cm 3 . Finally, the reason for limiting the composition of the alloy of the present invention will be described. First, in the Al--Ni vibration absorbing alloy of the present invention, Ni not only contributes to improving the damping capacity Q -1 but also strengthens the alloy. The reason for limiting the Ni content to 0.1 to 20% by weight is that if the lower limit of the composition is not met, sufficient damping ability for the purpose of the present invention cannot be obtained, and if the upper limit of the composition is exceeded, the damping ability deteriorates. This is also because cold working becomes impossible. In addition, in order to obtain the required damping ability, strength, and workability, sufficient homogeneous solution treatment is performed by heating at a temperature of 250°C or higher and lower than the melting point for a long time of 100 hours or less for homogeneous solution treatment. Absolutely necessary. Note that performing cold working at a cold working rate of 5% or more is an absolutely necessary condition for increasing the damping capacity by increasing the working strain and dislocation density. The alloy molded body is heated to 250℃ below the melting point of aluminum.
When homogeneous solid solution treatment is performed by heating at higher temperatures and for a longer period of time, the state of dispersion of Ni particles in the aluminum matrix becomes homogeneous. When this is subjected to cold working at a cold working rate of 5% or more, Ni particles are finely dispersed.
Dislocation density increases. When this dislocation density increases, when vibration is applied from the outside, the applied external force (vibration, impact, torsion, compression, tension, etc.) disappears as thermal energy etc., causing vibration damping. be. Therefore, in order to increase the attenuation capacity, it is necessary to
Long-term heating at higher temperatures and cold working of 5% or more are sufficient to achieve the objective, but when the cold working ratio is increased to 70% to 95%, and when alloys with a large amount of Ni are added. Depending on the composition of the
Some products are difficult to form by deep drawing, punching, etc. For this reason, when reheated for a long time at a low temperature of 250°C or lower, the damping capacity and strength do not deteriorate significantly, and forming processes such as bending, deep drawing, and punching become extremely easy. In this case, the reheating process is
If the temperature exceeds 250°C, the attenuation ability will decrease, which is not preferable. As mentioned above, the alloy of the present invention is characterized by having a large damping capacity, being lightweight, having good cold workability, high strength, and being non-ferromagnetic. Therefore, the synthesis of the present invention can be applied to various transportation systems, internal combustion engines for automobiles, large machines, moving parts of electronic equipment, parts operated by magnetic fields, various household goods, and structural materials for buildings, etc., and can be used to prevent vibration and noise, Very suitable for weight reduction.
第1図はAl−5%Ni合金につき500℃で5時間
加熱して徐冷後冷間加工したときの減衰能Q-1と
冷間加工率との関係を示す特性曲線図、第2図は
第1図と同じ合金の引張強度σtの冷間加工率との
関係を示す特性曲線図である。
Figure 1 is a characteristic curve diagram showing the relationship between damping capacity Q -1 and cold working rate when an Al-5%Ni alloy is heated at 500℃ for 5 hours, slowly cooled, and then cold worked. 2 is a characteristic curve diagram showing the relationship between the tensile strength σ t and the cold working rate of the same alloy as in FIG. 1. FIG.
Claims (1)
アルミニウムからなり、冷間加工率5%以上の冷
間加工により転位密度の増大した減衰能Q-1が6
×10-3以上であることを特徴とするAl−Ni吸振
合金。 2 重量比にて、ニツケル0.1〜20%および残部
アルミニウムから成る合金に、 (A) 合金の融点以下250℃以上の温度で5分間以
上100時間以下加熱後急冷するかあるいは毎秒
1℃以下の速度で徐冷した後、 (B) 冷間加工率5%以上の加工を施すことにより
減衰能Q-1が6×10-3以上とすることを特徴と
するAl−Ni吸振合金の製造方法。 3 重量比にて、ニツケル0.1〜20%および残部
アルミニウムよりなる合金に、 (A) 合金の融点以下250℃以上の温度で5分間以
上100時間以下加熱し、急冷又は毎秒1℃以下
の速度で徐冷した後、 (B) 冷間加工率5%以上の加工を施す (C) (B)の冷間加工率5%以上の加工を施したもの
を250℃以下の温度で1分間以上500時間以下加
熱して急冷するか毎秒1℃以下の速度で徐冷す
る の順序で熱処理を施すことにより減衰能Q-1を6
×10-3以上とすることを特徴とするAl−Ni吸振
合金の製造方法。 4 溶解に際し、遮断剤としてMgCl2、硼砂、
CaF2、KClより選ばれた全量5%以上のフラツ
クスを加える特許請求の範囲第2項および第3項
の何れかに記載のAl−Ni吸振合金の製造方法。 5 溶解に際し、Mg、Beより選ばれた全量0.5
%以下の脱酸剤を添加する特許請求の範囲第2項
および第3項の何れかに記載のAl−Ni吸振合金
の製造方法。[Claims] 1. Consists of 0.1 to 20% nickel and the balance aluminum by weight, and has a damping capacity Q -1 of 6 with an increased dislocation density due to cold working at a cold working rate of 5% or more.
An Al-Ni vibration-absorbing alloy characterized by having a resistance of ×10 -3 or more. 2. An alloy consisting of 0.1 to 20% nickel and the balance aluminum by weight is heated at a temperature of (A) below the melting point of the alloy or above 250°C for 5 minutes to 100 hours and then rapidly cooled or at a rate of 1°C per second or below. (B) A method for producing an Al-Ni vibration absorbing alloy, characterized in that the damping capacity Q -1 is made to be 6×10 -3 or more by performing slow cooling at a cold working rate of 5% or more. 3 An alloy consisting of 0.1 to 20% nickel and the balance aluminum by weight is heated at a temperature of (A) below the melting point of the alloy or above 250°C for 5 minutes or more and 100 hours or less, and then rapidly cooled or at a rate of 1°C per second or less. After slow cooling, (B) Processing with a cold working rate of 5% or more (C) Processing of (B) with a cold working rate of 5% or more at a temperature of 250°C or less for 1 minute or more 500°C The damping capacity Q -1 can be reduced to 6 by applying heat treatment in the order of heating for less than 1 hour and rapid cooling, or slow cooling at a rate of 1°C or less per second.
A method for producing an Al-Ni vibration absorbing alloy, characterized in that it has a vibration absorbing alloy of ×10 -3 or more. 4. MgCl 2 , borax,
A method for producing an Al-Ni vibration absorbing alloy according to any one of claims 2 and 3, in which a total amount of 5% or more of flux selected from CaF 2 and KCl is added. 5 During dissolution, the total amount selected from Mg and Be is 0.5
% or less of a deoxidizing agent is added.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2367987A JPS62188763A (en) | 1987-02-05 | 1987-02-05 | Al-ni-base high-damping alloy and its production |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2367987A JPS62188763A (en) | 1987-02-05 | 1987-02-05 | Al-ni-base high-damping alloy and its production |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11720479A Division JPS5641346A (en) | 1979-09-14 | 1979-09-14 | A -ni damping alloy and its manufacture |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62188763A JPS62188763A (en) | 1987-08-18 |
| JPH0327620B2 true JPH0327620B2 (en) | 1991-04-16 |
Family
ID=12117154
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2367987A Granted JPS62188763A (en) | 1987-02-05 | 1987-02-05 | Al-ni-base high-damping alloy and its production |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS62188763A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5641346A (en) * | 1979-09-14 | 1981-04-18 | Res Inst Electric Magnetic Alloys | A -ni damping alloy and its manufacture |
| JP7329966B2 (en) * | 2019-05-23 | 2023-08-21 | 株式会社Uacj | Aluminum alloy material |
-
1987
- 1987-02-05 JP JP2367987A patent/JPS62188763A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62188763A (en) | 1987-08-18 |
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