JPS6144143B2 - - Google Patents
Info
- Publication number
- JPS6144143B2 JPS6144143B2 JP843184A JP843184A JPS6144143B2 JP S6144143 B2 JPS6144143 B2 JP S6144143B2 JP 843184 A JP843184 A JP 843184A JP 843184 A JP843184 A JP 843184A JP S6144143 B2 JPS6144143 B2 JP S6144143B2
- Authority
- JP
- Japan
- Prior art keywords
- alloy
- damping capacity
- cold working
- alloys
- damping
- 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
Links
- 229910045601 alloy Inorganic materials 0.000 claims description 40
- 239000000956 alloy Substances 0.000 claims description 40
- 238000013016 damping Methods 0.000 claims description 37
- 238000005482 strain hardening Methods 0.000 claims description 29
- 239000011701 zinc Substances 0.000 claims description 13
- 238000010438 heat treatment Methods 0.000 claims description 8
- 229910052725 zinc Inorganic materials 0.000 claims description 7
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 5
- 229910052782 aluminium Inorganic materials 0.000 claims description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 5
- 238000001816 cooling Methods 0.000 claims description 3
- 238000000265 homogenisation Methods 0.000 claims description 3
- 238000002844 melting Methods 0.000 claims description 3
- 230000008018 melting Effects 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 238000011282 treatment Methods 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 229910018137 Al-Zn Inorganic materials 0.000 description 7
- 229910018573 Al—Zn Inorganic materials 0.000 description 7
- 239000013078 crystal Substances 0.000 description 7
- 230000005484 gravity Effects 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 239000012071 phase Substances 0.000 description 5
- 229910002056 binary alloy Inorganic materials 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 238000010586 diagram Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- KHYBPSFKEHXSLX-UHFFFAOYSA-N iminotitanium Chemical compound [Ti]=N KHYBPSFKEHXSLX-UHFFFAOYSA-N 0.000 description 3
- 229910001000 nickel titanium Inorganic materials 0.000 description 3
- 238000010583 slow cooling Methods 0.000 description 3
- 238000005452 bending Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 238000004080 punching Methods 0.000 description 2
- 238000010791 quenching Methods 0.000 description 2
- 239000006104 solid solution Substances 0.000 description 2
- 229910018182 Al—Cu Inorganic materials 0.000 description 1
- 229910004261 CaF 2 Inorganic materials 0.000 description 1
- 229910000881 Cu alloy Inorganic materials 0.000 description 1
- 229910002482 Cu–Ni Inorganic materials 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 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
- 239000002981 blocking agent Substances 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 230000005294 ferromagnetic effect Effects 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 238000005242 forging Methods 0.000 description 1
- 239000007789 gas Substances 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
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 230000005291 magnetic effect Effects 0.000 description 1
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M potassium chloride Inorganic materials [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
Landscapes
- Heat Treatment Of Nonferrous Metals Or Alloys (AREA)
- Powder Metallurgy (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、また生活環境に存在する
種々な振動や騒音公害を防止するのに最適な振動
減衰能の大きな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1サイクル中に失われる振動エネル
ギーΔEおよび全振動エゾネルギー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動の振
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Alを基としてこれに重量比2〜82%の亜鉛を
加えた二元合金に冷間加工率5%以上の冷間加工
を施して結晶粒を微細化させると同時に転位を増
加させ、結晶粒の粒界効果と転位の履歴現象によ
つて大きな減衰能と高い強度をもたせた吸振合金
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
よつて溶解した後充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。
なお、この溶解する際に、遮断剤として
MgCl2、硼砂、CaF2,KCl,ZnCl2などの全量5
%以下のフラツクスおよび脱酸剤としてマグネシ
ウム、ベリウム等の脱酸剤を0.5%以下加えても
よい。
次にこの鋳塊に次のごとき工程を施す。
(A) 均質化処理のため、その合金の融点以下250
℃以上の温度で5分間以上(好ましくは30分〜
100時間位)加熱した後、急冷するあるいは毎
秒1℃以下の速度で徐冷する。つづいて常温に
おいて鍛造、圧延、押出、スエジングあるいは
引き抜きなどの冷間加工を少くとも5%以上の
冷間加工率によつて施す。
(B) 次いで、250℃以下の温度で5分以上100時間
以下加熱し常温迄急冷するか徐冷する。
工程(A)において均質化処理するのは溶湯凝固の
際の鋳塊各部の温度差や固液両相の比重差に基ず
いて鋳塊に成分の不均質が起ることがあるから、
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、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。これは溶体化処理を十
分に行なわなければ、減衰能などの製品の性能を
均一にすることができないときもあるからであ
る。
次に(A)において、冷間加工するのは加工歪みに
よつて結晶粒を微細化させ転位密度を増大させ
る。その結果結晶粒界の移動と転位の履歴現象に
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
冷間加工を施すことだけで充分その目的が達せら
れるが、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
に工程(B)において、冷間加工後に250℃以下の温
度に加熱するのは曲げ、深絞り、打ち抜きなどの
成形を容易にするためである。ここで250℃以下
とした理由は250℃以上にここで再加熱すると減
衰能が低下するためである。
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Ar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350℃で5時間加熱し
て徐冷した後350℃で1時間の中間熱処理を施し
ながら冷間スエージングおよび引抜きにより1.1
mm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の測定は逆吊り捩り振
子法により振動数約1Hz、最大歪み振幅γm=10
×10-6で行なつた。
Al基合金の減衰能Q-1ならびに強度は冷間加工
率に依存する。第1図および第2図にはその一例
として試料No.1,No.2,No.4,No.6,No.8及びNo.
9合金を350℃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と冷間加工率との関係が、同様に第2図
には試料No.6合金の引張強度σtと冷間加工率と
の関係が示してある。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結晶
粒が微細化され、転位密度が増大した結果を示す
ものである。
本発明の目的とする減衰能Q-1=6×10-3以上
(γm=10×10-6)を得るには少くとも5%以上
の冷間加工を施す必要があり、冷間加工はできる
だけ大きい方がよく、99.99%でもよい。冷間加
工率は(πD2−πd2)/πD2×100(%)である
ので、10
mm径のものが0.1mm径迄減面加工されるとその加
工率は99.99%となる。
次にAl−Zn二元合金について350℃から徐冷後
冷間加工率95%で加工したときの減衰能Q-1およ
び比重ρを示すと第1表のとおりである。
The present invention is designed to prevent pollution caused by vibrations and noises of various transportation systems and large machines, performance deterioration caused by vibrations of various precision machines and electronic devices, and vibrations that are optimal for preventing various vibrations and noise pollution that exist in the living environment. This relates to a vibration-absorbing alloy with large damping ability. The damping capacity Q -1 , which is generally used to compare damping capacities, has a relationship with the vibrational energy ΔE lost during one cycle of vibration 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 of vibration 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 high damping ability, but their specific gravity is around 8 g/ cm3 , making them unsuitable when reducing the weight of equipment.Al-Cu-Ni Ni-Ti alloys and Ni-Ti alloys have the disadvantage that cold working is not possible at all. In order to obtain a vibration-absorbing alloy that is lighter than conventional vibration-absorbing alloys, we developed a binary alloy based on Al, which has a very small specific gravity of 2.7 g/cm 3 , and added zinc in a weight ratio of 2 to 82%. Cold working is applied at a cold working rate of 5% or more to refine the crystal grains and increase dislocations, resulting in large damping capacity and high strength due to the grain boundary effect of the crystal grains and the hysteresis phenomenon of dislocations. The purpose of the present invention is to provide a vibration-absorbing alloy that has a vibration-absorbing effect. 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 thoroughly stirred to make 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. In addition, during this dissolution, it is used as a blocking agent.
Total amount of MgCl 2 , borax, CaF 2 , KCl, ZnCl 2 etc. 5
% or less of flux and a deoxidizing agent such as magnesium or beryum may be added in an amount of 0.5% or less as a deoxidizing agent. Next, this ingot is subjected to the following steps. (A) 250 below the melting point of the alloy due to homogenization
At a temperature of ℃ or higher for 5 minutes or more (preferably 30 minutes or more)
After heating (about 100 hours), cool rapidly or slowly at a rate of 1°C per second or less. Subsequently, cold working such as forging, rolling, extrusion, swaging, or drawing is performed at room temperature at a cold working rate of at least 5%. (B) Next, heat at a temperature of 250°C or lower for 5 minutes or more and 100 hours or less, and then quench or slowly cool to room temperature. The reason why homogenization treatment is performed in step (A) is that non-uniformity of components may occur in the ingot due to temperature differences between different parts of the ingot and differences in specific gravity between the solid and liquid phases during molten metal solidification.
This is to make the ingredients homogeneous. If the heating temperature is high, the heating time can be shortened, and if the weight of the molded product is large, it is necessary to increase the heating temperature and lengthen the heating time. This is because unless the solution treatment is sufficiently performed, it may not be possible to make the performance of the product, such as the damping capacity, uniform. Next, in (A), cold working refines crystal grains and increases dislocation density due to processing strain. As a result, this is an essential step in order to obtain the large damping ability that is the object of the present invention due to the movement of grain boundaries and the hysteresis phenomenon of dislocations, and also to increase the tensile strength of the molded body. In addition, in order to increase the damping capacity, cold working of 5% or more is sufficient to achieve the objective, but depending on the composition of the alloy, forming by bending, deep drawing, punching, etc. may be difficult. There is. For this purpose, in step (B), the reason why the material is heated to a temperature of 250° C. or less after cold working is to facilitate forming such as bending, deep drawing, and punching. The reason why the temperature is set at 250°C or lower is that the attenuation ability decreases if the temperature is reheated to 250°C or higher. A total of 100 g of metal with the composition shown in Table 1 was melted in an alumina crucible in a high-frequency induction electric furnace while passing Ar gas to the surface, and cast into an iron mold with a diameter of 10 mm.
An ingot was obtained. Next, this was heated at 350°C for 5 hours, slowly cooled, and then subjected to intermediate heat treatment at 350°C for 1 hour, cold swaging and drawing to 1.1
mm wire, and cut a 150 mm long wire from it to use as a sample. The damping capacity Q -1 was measured using the inverted torsion pendulum method at a frequency of approximately 1 Hz and a maximum strain amplitude γm = 10.
It was carried out at ×10 -6 . The damping capacity Q -1 and strength of Al-based alloys depend on the cold working rate. Examples of samples No. 1, No. 2, No. 4, No. 6, No. 8, and No. 8 are shown in FIG. 1 and FIG. 2.
Similarly, Figure 2 shows the relationship between damping capacity Q -1 and cold working rate when 9 alloys were heated at 350°C for 5 hours, slowly cooled, and processed by cold swaging and drawing. The relationship between the tensile strength σ t and cold working rate of No. 6 alloy is shown. Both the damping capacity Q -1 and the tensile strength σ t increase as the cold working rate increases, indicating that the grains become finer and the dislocation density increases as the working strain increases. . In order to obtain the damping capacity Q -1 = 6 x 10 -3 or more (γm = 10 x 10 -6 ) which is the objective of the present invention, it is necessary to perform cold working of at least 5% or more. It is better to make it as large as possible, even 99.99%. Since the cold working rate is (πD 2 −πd 2 )/πD 2 ×100 (%), when a 10 mm diameter piece is reduced in area to a 0.1 mm diameter, the working rate is 99.99%. Next, Table 1 shows the damping capacity Q -1 and specific gravity ρ when processing the Al-Zn binary alloy at a cold working rate of 95% after slow cooling from 350°C.
【表】
第1表に示した批較試料No.1の通常の不純物を
含む純Alは冷間加工率95%を施した状態で減衰
能Q-1が4×10-3でZnの入らない純アルミニウム
では本発明の目的とする吸振材料として不適当で
あるが、Alに2%以上のZnを添加すると本発明
の目的とする減衰能Q-1=6×10-3以上の値を得
ることができ、かなり大きな減衰能が得られる。
要するに本発明合金の減衰能Q-1の値は一般の
金属のQ-1=1×10-3の値に比較して数十倍大き
いことがわかる。さらに本発明合金の比重ρも一
般の金属に比べてかなり小さく、その引張強度σ
tは冷間加工した比較試料No.1の純Alのσt=10
Kg/mm2に対してかなり大きい。また比重ρは比較
試料No.3の6.3g/cm2に比べてかなり小さい。例
えば実施例の試料No.6はσt=24Kg/mm2,ρ=4.0
g/cm3、試料No.8はσt=13Kg/mm2,ρ=4.8g/
cm3である。
なおAl−Zn合金の減衰能Q-1とZn量との関係
を示すと第3図のとおりである。ここで減衰能Q
-1は350℃から徐冷或いは急冷したときの値と徐
冷後に71%および95%の冷間加工率で冷間加工し
たとき並びに急冷後95%の冷間加工率で冷間加工
したときの値である。
ここでAl−Zn系の非常に大きい減衰能Q-1の
起因について述べる。Alに対するZnの固溶限は
常温で非常に小さいためAl側固溶体α相とZn側
固溶体β相の二相組織になつている。熱処理した
Al−Zn合金はα相とβ相の結晶粒が混合してい
るが、これに応力(振動的)が加わつたときに粒
界で結晶粒が粘性的な移動をするためにエネルギ
ーが失なわれる。その結果減衰能Q-1が生じる。
熱処理したAl−Zn系合金に冷間加工を施すと結
晶粒が粉砕、即ち微細化されると同時に合金内に
転位が多く導入される。結晶粒が微細化されると
粒界が多くなるため粒界での粘性的移動による減
衰能Q-1は大きくなる。また転位の運動に対して
溶質原子や不純物原子はPinning(Granat−
Liickeの理論として公知である)として作用して
応力−歪み曲線に履歴が生じ、この履歴が減衰能
Q-1の原因となる。それ故冷間加工によつて転位
が多くなると、その履歴による減衰能Q-1が大き
くなるわけである。したがつてAl−Zn二元合金
の減衰能Q-1は350℃から徐冷したときには第3
図に見るようにかなり小さいが、急冷したときに
は第3図に見るようにかなり小さいが、急冷した
ときにはZn70〜95%を含む合金でやや大きくな
り、約65%Zn以下を含む合金では小さくなる。
これらの熱処理後に95%と71%の冷間加工を施し
たときの減衰能Q-1は非常に大きくなり、95%と
71%の冷間加工とでは大して差がないが、冷間加
工率の大きい程よい結果が得られる。
本発明合金の組成を限定した理由について述べ
る。まず二元合金において亜鉛は減衰能Q-1の向
上に寄与するばかりでなく、合金の強度を向上す
る。亜鉛を重量比2〜82%と限定したのはこの組
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
を越えるときには比較試料No.3のように比重ρが
6.3g/cm3でρが大きくなりすぎるからである。
従つて本発明合金の特徴は減衰能が大きいこ
と、軽量であること、冷間加工性が良好で強化し
ている上に非強磁性であることである。本発明は
これらの利点をもつことは各種の交通機関や大型
機械の材料、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材料などへ応用
して振動および騒音の防止、軽量化を計るのに非
常に適しており、斯種工業に応用して極めて有用
である。[Table] The comparison sample No. 1 shown in Table 1, pure Al containing normal impurities, had a damping capacity Q -1 of 4 × 10 -3 with a cold working rate of 95% and did not contain Zn. Pure aluminum is not suitable as a vibration absorbing material for the purpose of the present invention, but when 2% or more of Zn is added to Al, the value of damping capacity Q -1 = 6 × 10 -3 or more, which is the purpose of the present invention, can be achieved. It is possible to obtain a considerably large attenuation capacity. In short, it can be seen that 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 Q -1 =1×10 -3 of general metals. Furthermore, the specific gravity ρ of the alloy of the present invention is considerably smaller than that of general metals, and its tensile strength σ
t is σ t = 10 of cold-worked pure Al of comparison sample No. 1
Quite large compared to Kg/mm 2 . Further, the specific gravity ρ is considerably smaller than 6.3 g/cm 2 of comparative sample No. 3. For example, sample No. 6 of the example has σ t =24Kg/mm 2 and ρ = 4.0
g/cm 3 , sample No. 8 has σ t = 13Kg/mm 2 , ρ = 4.8g/
cm3 . The relationship between the damping capacity Q -1 of the Al-Zn alloy and the amount of Zn is shown in Figure 3. Here, the damping capacity Q
-1 is the value when slowly or rapidly cooled from 350℃, when cold worked at a cold working rate of 71% and 95% after slow cooling, and when cold worked at a cold working rate of 95% after rapid cooling. is the value of Here, we will discuss the cause of the extremely large attenuation capacity Q -1 of the Al-Zn system. Since the solid solubility limit of Zn in Al is very small at room temperature, it has a two-phase structure consisting of an α phase as a solid solution on the Al side and a β phase as a solid solution on the Zn side. heat treated
Al-Zn alloys have a mixture of α-phase and β-phase crystal grains, but when stress (vibration) is applied to this, the crystal grains move viscous at the grain boundaries, causing energy loss. be exposed. As a result, a damping capacity Q -1 is generated.
When a heat-treated Al-Zn alloy is subjected to cold working, the crystal grains are crushed, that is, refined, and at the same time many dislocations are introduced into the alloy. As the crystal grains become finer, the number of grain boundaries increases, so the damping capacity Q -1 due to viscous movement at the grain boundaries increases. In addition, solute atoms and impurity atoms are affected by Pinning (Granat-
(known as Liicke's theory), a history is generated in the stress-strain curve, and this history is the cause of the damping capacity Q -1 . Therefore, when the number of dislocations increases due to cold working, the damping capacity Q -1 due to the history increases. Therefore, the damping capacity Q -1 of the Al-Zn binary alloy becomes 3rd when gradually cooled from 350℃.
As shown in the figure, it is quite small, but when rapidly cooled, it is quite small as shown in Figure 3, but when rapidly cooled, it becomes slightly larger in alloys containing 70 to 95% Zn, and becomes smaller in alloys containing less than about 65% Zn.
When 95% and 71% cold working is performed after these heat treatments, the damping capacity Q -1 becomes very large, and 95% and 71% cold working are performed.
Although there is not much difference from cold working at 71%, the higher the cold working rate, the better the results. The reason for limiting the composition of the alloy of the present invention will be described. First, in binary alloys, zinc not only contributes to improving the damping capacity Q -1 but also improves the strength of the alloy. The reason why the weight ratio of zinc is limited to 2 to 82% is because if the lower limit of the composition is not reached, the sufficient damping ability aimed at by the present invention cannot be obtained, and if the above upper limit of the composition is exceeded, the weight ratio of comparative sample No. 3 is So the specific gravity ρ is
This is because ρ becomes too large at 6.3 g/cm 3 . Therefore, the characteristics of the alloy of the present invention are that it has a large damping capacity, is lightweight, has good cold workability, is reinforced, and is non-ferromagnetic. The present invention has these advantages and can be applied to materials for various transportation systems and large machines, moving parts of electronic devices, parts operated by magnetic fields, various household items, and building materials, etc., to prevent vibration and noise, and to be lightweight. It is very suitable for measuring the conversion rate, and is extremely useful when applied to this type of industry.
第1図は試料No.1,No.2,No.4,No.6,No.8及
びNo.9合金を350℃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
を示す曲線図、第2図は第1図中の試料No.6合金
の引張強度σtと冷間加工率との関係を示す曲線
図、第3図はAl−Zn合金の350℃から徐冷及び急
冷したときの減衰能Q-1と、徐冷及び急冷後夫々
71%および95%の冷間加工率で冷間加工したとき
並びに急冷後95%の冷間加工率で冷間加工したと
きの減衰能Q-1とZn量との関係を示す特性曲線図
である。
Figure 1 shows the damping capacity Q of sample No. 1, No. 2, No. 4, No. 6, No. 8, and No. 9 alloys when they were heated at 350℃ for 5 hours, slowly cooled, and then cold worked. Figure 2 is a curve diagram showing the relationship between -1 and cold working rate. Figure 2 is a curve diagram showing the relationship between tensile strength σ t and cold working rate of sample No. 6 alloy in Figure 1. are the damping capacity Q -1 of the Al-Zn alloy when slowly and rapidly cooled from 350℃, and the damping capacity Q -1 after slow cooling and rapid cooling, respectively.
This is a characteristic curve diagram showing the relationship between damping capacity Q -1 and Zn content when cold worked at a cold working rate of 71% and 95%, and when cold worked at a cold working rate of 95% after quenching. be.
Claims (1)
ニウムからなり、結晶粒を微細化した組織を有
し、かつ減衰能Q-1が6×10-3以上であることを
特徴とする減衰能が大きなアルミニウム基吸振合
金。 2 重量比にて亜鉛2〜82%および残部アルミニ
ウムより成る合金について、 (A) 合金の融点以下250℃以上の温度で5分間以
上100時間以下加熱して均質化処理し、冷却し
た後少なくとも5%以上の冷間加工率で加工す
る。 (B) 次いで、250℃以下の温度で5分間以上100時
間以下加熱して冷却する。 工程を順次施すことにより結晶粒を微細化した組
織を有し、かつ減衰能Q-1が6×10-3以上の合金
を得ることを特徴とする減衰能が大きなアルミニ
ウム基吸振合金の製造方法。[Claims] 1. Consists of 2 to 82% zinc and the balance aluminum by weight, has a structure with fine grains, and has a damping capacity Q -1 of 6 × 10 -3 or more. An aluminum-based vibration absorbing alloy with high damping ability. 2 For alloys consisting of 2 to 82% zinc and the balance aluminum by weight, (A) Homogenization treatment by heating at a temperature of 250°C or below the melting point of the alloy for 5 minutes or more and 100 hours or less, and after cooling, at least 5% Process at a cold working rate of % or more. (B) Next, heat at a temperature of 250°C or less for 5 minutes or more and 100 hours or less, and then cool. A method for producing an aluminum-based vibration-absorbing alloy with a large damping capacity, characterized by obtaining an alloy having a structure with finer grains and a damping capacity Q -1 of 6 × 10 -3 or more by sequentially performing the steps. .
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP843184A JPS59162243A (en) | 1984-01-23 | 1984-01-23 | Vibration absorbing aluminum alloy having large damping capacity and its manufacture |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP843184A JPS59162243A (en) | 1984-01-23 | 1984-01-23 | Vibration absorbing aluminum alloy having large damping capacity and its manufacture |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP54108079A Division JPS607018B2 (en) | 1979-08-27 | 1979-08-27 | Aluminum-based vibration absorbing alloy with large damping capacity and its manufacturing method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59162243A JPS59162243A (en) | 1984-09-13 |
| JPS6144143B2 true JPS6144143B2 (en) | 1986-10-01 |
Family
ID=11692932
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP843184A Granted JPS59162243A (en) | 1984-01-23 | 1984-01-23 | Vibration absorbing aluminum alloy having large damping capacity and its manufacture |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59162243A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH047970Y2 (en) * | 1985-06-25 | 1992-02-28 | ||
| JPH0295996U (en) * | 1989-01-19 | 1990-07-31 | ||
| KR101488288B1 (en) * | 2012-11-20 | 2015-01-30 | 현대자동차주식회사 | Vibration damping aluminum alloy |
-
1984
- 1984-01-23 JP JP843184A patent/JPS59162243A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59162243A (en) | 1984-09-13 |
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