JPS6242984B2 - - Google Patents
Info
- Publication number
- JPS6242984B2 JPS6242984B2 JP11276079A JP11276079A JPS6242984B2 JP S6242984 B2 JPS6242984 B2 JP S6242984B2 JP 11276079 A JP11276079 A JP 11276079A JP 11276079 A JP11276079 A JP 11276079A JP S6242984 B2 JPS6242984 B2 JP S6242984B2
- Authority
- JP
- Japan
- Prior art keywords
- less
- alloy
- temperature
- cold working
- heating
- 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 39
- 239000000956 alloy Substances 0.000 claims description 39
- 238000013016 damping Methods 0.000 claims description 27
- 238000005482 strain hardening Methods 0.000 claims description 25
- 238000010438 heat treatment Methods 0.000 claims description 22
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 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
- 229910052742 iron Inorganic materials 0.000 claims description 7
- 238000002844 melting Methods 0.000 claims description 7
- 230000008018 melting Effects 0.000 claims description 7
- 229910052787 antimony Inorganic materials 0.000 claims description 6
- 229910052758 niobium Inorganic materials 0.000 claims description 6
- 239000010955 niobium Substances 0.000 claims description 6
- 239000010936 titanium Substances 0.000 claims description 6
- 229910052719 titanium Inorganic materials 0.000 claims description 6
- 229910052726 zirconium Inorganic materials 0.000 claims description 6
- 229910018185 Al—Co Inorganic materials 0.000 claims description 5
- 239000011575 calcium Substances 0.000 claims description 5
- 229910052791 calcium Inorganic materials 0.000 claims description 5
- 229910052715 tantalum Inorganic materials 0.000 claims description 5
- 229910052684 Cerium Inorganic materials 0.000 claims description 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 4
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 4
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims description 4
- 229910052796 boron Inorganic materials 0.000 claims description 4
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 claims description 4
- 239000010941 cobalt Substances 0.000 claims description 4
- 229910017052 cobalt Inorganic materials 0.000 claims description 4
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 239000000463 material Substances 0.000 claims description 4
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 claims description 4
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 claims description 4
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 3
- 238000001816 cooling Methods 0.000 claims 6
- 230000007423 decrease Effects 0.000 description 7
- 238000000137 annealing Methods 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 238000005452 bending Methods 0.000 description 5
- 238000004080 punching Methods 0.000 description 5
- 230000005484 gravity Effects 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 229910000640 Fe alloy Inorganic materials 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000012456 homogeneous solution Substances 0.000 description 2
- 238000000265 homogenisation Methods 0.000 description 2
- KHYBPSFKEHXSLX-UHFFFAOYSA-N iminotitanium Chemical compound [Ti]=N KHYBPSFKEHXSLX-UHFFFAOYSA-N 0.000 description 2
- 230000006698 induction Effects 0.000 description 2
- 229910052745 lead Inorganic materials 0.000 description 2
- 229910001000 nickel titanium Inorganic materials 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 238000003303 reheating Methods 0.000 description 2
- 239000000243 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
- 239000011358 absorbing material Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000002981 blocking agent Substances 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000002485 combustion reaction Methods 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
- 238000002474 experimental method 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
- 230000009931 harmful effect Effects 0.000 description 1
- 239000011261 inert gas 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
- 238000005259 measurement Methods 0.000 description 1
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M potassium chloride Inorganic materials [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
Landscapes
- Fluid-Damping Devices (AREA)
- Heat Treatment Of Nonferrous Metals Or Alloys (AREA)
Description
本発明は各種の交通機関、大型機械の振特およ
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−Co基吸振合金およびその製造方
法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△E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・△E/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%のコバルトと50%以下の鉛、アンチモン、40
%以下のセリウム、20%以下のタンタル、15%以
下の鉄、ニオブ、ジルコニウム、10%以下のチタ
ン、カルシウム、3%以下の硼素のうち1種又は
2種以上の全量0.1〜50%を加えた多元合金に冷
間加工率5%以上の加工を施して転位を増加さ
せ、その履歴現象によつて大きな減衰能をもたせ
ると同時に強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、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。
次にこの鋳塊に次のごとき熱処理を施す。
(A) 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(好ましくは30分以上100時間以下)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%以上の冷間加工を施した
ものを250℃以下の温度で1分間以上(好好ま
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などの金属を
全量で0.5%以下を加えてもよい。
工程(A)において均質化処理するのは鋳塊に成分
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、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、均質溶体化処理を充分に行わなければ、
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。
工程(A)において均質化処理の後に工程(B)の冷間
加工するのは加工歪によつて転位密度を増大さ
せ、転位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こ
とだけで充分その目的が達せられるが、冷間加工
率の大きい場合又は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。
従つて、工程(B)において冷間加工したものを
250℃以下の温度に加熱すると、常温において曲
げ、深絞り、打ち抜きなどの成形が一層容易にな
る。ここで焼鈍温度を250℃以下としたのは、250
℃以上に加熱すると、伸びが急激に増大するが減
衰能が低下するからである。
実施例 1
第1表〜第2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、鋳型に鋳込んで
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150
mm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−Co合金に種々の他元素を1種又は2種以
上添加した多元合金について冷間加工率95%を施
したときのQ-1の値は第1表および第2表に示し
たとおりである。
The present invention is designed to reduce vibrations that are most suitable for preventing pollution caused by the vibrations and noise of various transportation systems and large machines, performance deterioration caused by vibrations of various precision machines and electronic equipment, and the harmful effects of various vibrations and noises that exist in the living environment. This invention relates to an Al-Co-based vibration absorbing alloy with high damping ability and a method for manufacturing the same. Attenuation capacity generally used to compare attenuation capacity
Q -1 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 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
20% cobalt and less than 50% lead, antimony, 40
% or less of cerium, 20% or less of tantalum, 15% or less of iron, niobium, zirconium, 10% or less of titanium, calcium, and 3% or less of boron in a total amount of 0.1 to 50%. The object of the present invention is to provide a vibration-absorbing alloy which has a large damping ability and strong strength by subjecting a multi-component alloy to cold working at a cold working rate of 5% or more to increase dislocations and, through the hysteresis phenomenon, to have a large damping ability and 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 thoroughly stirred to make a uniform molten metal, which is then cast into a sand mold or metal mold. Make ingots. Next, this ingot is subjected to the following heat treatment. (A) After heating for solution treatment at a temperature as high as possible, for example, at a temperature of 250°C or higher below the melting point of the alloy for 5 minutes or more (preferably 30 minutes or more and 100 hours or less), rapidly cool it or at a rate of 1°C per second or less. Cool slowly. (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 cold worked with a cold working rate of 5% or more in (B) is heated at a temperature of 250°C or less for 1 minute or more (preferably 30 minutes or more and 500 hours or less) and then rapidly cooled or cooled every second. Cool slowly at a rate of 1°C or less. When melting, add flux such as MgCl 2 , borax, CaF 2 , KCl, etc. in a total amount of 5% or less as a blocking agent, and add metals such as Mg, Be, etc. in a total amount of 0.5% or less as a deoxidizing agent. Good too. The reason why the homogenization treatment is carried out in step (A) is to make the components homogeneous since non-uniformity of components may occur in the ingot. 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, it is necessary to raise the heating temperature and increase the heating time, but if the weight of the molded object is small, it may be heated at a relatively low temperature for a short time. The reason for this is that if homogeneous solution treatment is not performed sufficiently,
This is because product performance such as damping capacity cannot be made uniform. The cold working in step (B) after the homogenization treatment in step (A) is an essential step in order to increase the dislocation density due to processing strain and to obtain a large damping capacity due to the dislocation hysteresis phenomenon. It is also necessary to increase the tensile strength of the molded article. In addition, in order to increase the damping capacity, cold working of 5% or more is enough to achieve the purpose, but if the cold working rate is large or depending on the composition of the alloy, bending,
Some products are difficult to form by deep drawing, punching, etc. Therefore, the cold processed material in step (B)
Heating to a temperature of 250°C or lower makes it easier to form such things as bending, deep drawing, and punching at room temperature. Here, the annealing temperature was set to 250℃ or less because 250
This is because heating to a temperature higher than 0.degree. C. causes a rapid increase in elongation, but a decrease in damping ability. Example 1 Total amount of metal with the composition shown in Tables 1 and 2: 100g
was melted in an alumina crucible using a high-frequency induction electric furnace while passing Ar gas through the surface, and poured into a mold to obtain an ingot with a diameter of 10 mm. Next, this was heated at 500℃ for 5 hours and slowly cooled, and then cold swaged and drawn into a 1.1mm wire.
A mm line was cut and used 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 . Tables 1 and 2 show the values of Q -1 when a 95% cold working rate is applied to a multi-component alloy in which one or more of various other elements are added to an Al-Co alloy. be.
【表】【table】
【表】
これらの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%以上のコバルトならび
に他の元素の1種又は2種以上を全量で0.1%以
上添加すると本発明の目的とするQ-1が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。
実施例 2
Al−1.0%Co−0.5%Fe合金の全量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10
mm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、冷間加工率71%で冷間スエー
ジングおよび引抜きによつて1.1mmの線にした。
この冷間加工したものを150℃でそれぞれ60分、
180分焼鈍処理を施した後徐冷し、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。
その結果は第3表に示す通りである。[Table] As is clear from these tables, the cold working rate is 95%.
Aluminum treated with aluminum has a damping capacity Q -1 of 4 × 10 -3 and is unsuitable as a vibration absorbing material for the purpose of the present invention. When 0.1% or more of the total amount of
It can be seen that larger values 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. Example 2 A total of 100g of Al-1.0%Co-0.5%Fe alloy was melted in an alumina crucible using a high-frequency induction electric furnace while passing Ar gas to the surface, and cast into an iron mold to form a diameter of 10.
An ingot of mm was obtained. Next, this was heated at 500° C. for 5 hours, slowly cooled, and then cold swaged and drawn into a 1.1 mm wire at a cold working rate of 71%.
This cold processed material was heated to 150℃ for 60 minutes each.
After annealing for 180 minutes, it is slowly cooled and then the length
A 150 mm wire was cut and used as a sample. Attenuation capacity Q -1
The measurement was performed using an inverted torsional pendulum method at a frequency of approximately 1 Hz.
The experiment was carried out at a maximum strain amplitude γ n =10×10 -6 . The results are shown in Table 3.
【表】
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少なくとも3倍以上
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℃以上にあげ
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。
以上の試験の結果より、本発明合金の鋳塊に(A)
の熱処理を施して冷間加工率5%以上の冷間加工
を施した後250℃以下の温度で1分間以上500時間
以下加熱すると伸びElが大きくなり、曲げ、深
絞り、打ち抜き等の成形が容易になる。この実施
例2の場合のAl−1.0%Co−0.5%Fe合金につい
て冷間加工、加熱温度、加熱時間、伸びElと減
衰能Q-1との関係は第3表に示した通りで、加熱
温度が低いほど加熱時間を長くする必要がある。
更に加熱温度の上限を250℃としたのは250℃以上
にすると伸びElは25%以上非常に大きくなるが
減衰能Q-1が急に低下して4×10-3以下となるの
で本発明の目的には不充分となるからである。
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、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No.6はσt=18Kg/mm2、ρ=2.8
g/cm3、試料No.9はσt=25Kg/mm2、ρ=2.8g/
cm3、試料No.16はσt=20Kg/mm2、ρ=3.0g/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。まず多元合金においてCoおよび他の
添加元素Pb、Sb、Ce、Ta、Fe、Nb、Zr、Ti、
Ca、Bはいずれも減衰能Q-1の向上に寄与するば
かりでなく、Pbを除いて合金を強化する。Coを
重量比で0.1〜20%ならびにPb、Sbを50%以下、
Ceを40%以下、Taを20%以下、Fe、Nb、Zrを15
%以下、Ti、Caを10%以下、Bを3%以下のう
ち1種又は2種以上の全量を0.1〜50%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
的とする充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Pbでは充分な強度が
得られなくなり、また他の元素では冷間加工が不
可能となるからである。
本発明の吸振合金における各成分元素の成分範
囲が減衰能、機械的強度、加工性等に及ぼす一般
的傾向は第4表の通りである。[Table] 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, the brittleness decreases, and the workability decreases.
It is necessary to anneal at a temperature below 250℃. When annealing at a temperature of 250°C or lower, the elongation increases by at least three times, making it easier to process, and the damping ability 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. Note that when the annealing temperature is raised to 250° C. or higher, the elongation increases rapidly to 25% or higher, but the damping capacity Q −1 becomes 4×10 −3 or lower, and the object of the present invention cannot be obtained. From the results of the above tests, the ingot of the alloy of the present invention (A)
After cold working with a cold working ratio of 5% or more, heating at a temperature of 250°C or less for 1 minute or more and 500 hours or less increases the elongation El, making it difficult to form by bending, deep drawing, punching, etc. becomes easier. The relationship between cold working, heating temperature, heating time, elongation El, and damping capacity Q -1 for the Al-1.0%Co-0.5%Fe alloy in Example 2 is as shown in Table 3. The lower the temperature, the longer the heating time needs to be.
Furthermore, the upper limit of the heating temperature was set at 250°C because if the heating temperature is higher than 250°C, the elongation El becomes very large by 25% or more, but the damping capacity Q -1 suddenly decreases to 4 × 10 -3 or less, so this invention This is because it is insufficient for the purpose of Furthermore, the specific gravity ρ of the alloy of the present invention is considerably smaller than that of ordinary metals, and the tensile strength σ t is considerably larger than that of cold-worked aluminum, which is 10 Kg/mm 2 .
For example, sample No. 6 in the example has σ t = 18Kg/mm 2 and ρ = 2.8
g/cm 3 , sample No. 9 has σ t = 25Kg/mm 2 , ρ = 2.8g/
cm 3 , sample No. 16 has σ t = 20Kg/mm 2 , ρ = 3.0g/cm 3
It shows. Finally, the reason for limiting the composition of the alloy of the present invention will be described. First, in multi-component alloys, Co and other additive elements Pb, Sb, Ce, Ta, Fe, Nb, Zr, Ti,
Both Ca and B not only contribute to improving the damping capacity Q -1 but also strengthen the alloy except for Pb. Co 0.1 to 20% by weight, Pb and Sb 50% or less,
Ce: 40% or less, Ta: 20% or less, Fe, Nb, Zr: 15%
% or less, Ti, Ca 10% or less, and B 3% or less. This is because sufficient strength cannot be obtained with Pb when the above upper limit of the composition is exceeded, and cold working is impossible with other elements. Table 4 shows the general tendency that the component range of each component element in the vibration absorbing alloy of the present invention has on damping ability, mechanical strength, workability, etc.
【表】【table】
【表】
なお、均質溶体化処理のために250℃以上融点
以下の温度で長時間(100時間以下)加熱し、充
分な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は絶対必要であ
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ので絶対必要な条件で
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、アルミニウムのマトリツクス中のCoな
らびに副成分元素の粒子の分散の状態が均質とな
る。ここで冷間加工率5%以上の冷間加工を施す
と、Coならびに副成分元素粒子が微細に分散
し、転位密度が大となる。この転位密度が多くな
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、冷間加工率が大きい場合又は合金の組成によ
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
長時間再加熱して焼鈍処理をすると、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
場合の再加熱処理を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
て本発明合金は各種の交通機関、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] For homogeneous solution treatment, heating at a temperature of 250℃ or higher and lower than the melting point for a long time (100 hours or less) and sufficient solution treatment will reduce the required attenuation capacity.
It is absolutely necessary to obtain strength and workability. Note that performing cold working at a cold working rate of 5% or more is an absolutely necessary condition because it increases 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 the homogeneous solid solution treatment is performed by heating at the above high temperature for a long time, the state of dispersion of Co and subcomponent element particles in the aluminum matrix becomes homogeneous. When cold working is performed at a cold working rate of 5% or more, Co and subcomponent element particles are finely dispersed, and the dislocation density becomes large. When this dislocation density increases, the external force (vibration, shock, torsion, compression, tension, etc.) that is applied when vibration is applied from the outside
is annihilated as thermal energy and other energy, resulting in vibration damping. Therefore, in order to increase the attenuation capacity, it is necessary to
Long-term heating at higher temperatures and cold working of 5% or higher are enough to achieve the purpose; however, if the cold working rate is large or depending on the composition of the alloy, bending, deep drawing, punching, etc. Some products are difficult to mold. For this reason, when annealing is performed by reheating at a low temperature of 250°C or lower for a long period of time, 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, if the reheating treatment is carried out at a temperature of 250° C. or higher, 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 alloy of the present invention can be applied to various transportation systems, internal combustion engines for automobiles, large machinery, moving parts of electronic devices, 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.
Claims (1)
ンチモンの何れか1種又は2種50%以下、セリウ
ム40%以下、タンタル20%以下、鉄、ニオブ、ジ
ルコニウムの何れか1種又は2種以上15%以下、
チタン、カルシウムの何れか1種又は2種10%以
下、硼素3%以下の何れか1種又は2種以上の全
量0.1〜50%と残部アルミニウムからなり、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−Co基吸振合金。 2 重量比にて、コバルト0.1〜20%と、鉛、ア
ンチモンの何れか1種又は2種50%以下、セリウ
ム40%以下、タンタル20%以下、鉄、ニオブ、ジ
ルコニウムの何れか1種又は2種以上15%以下、
チタン、カルシウムの何れか1種又は2種10%以
下、硼素3%以下の何れか1種又は2種以上の全
量0.1〜50%および残部アルミニウムからなる合
金に、 (A) 合金の融点以下250℃以上の温度で5分間以
上100時間以下加熱して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を6×10-3以上とすることを特徴と
するAl−Co基吸振合金の製造方法。 3 重量比にて、コバルト0.1〜20%および残部
アルミニウムよりなる合金に、副成分として鉛、
アンチモンの何れか1種又は2種50%以下、セリ
ウム40%以下、タンタル20%以下、鉄、ニオブ、
ジルコニウムの何れか1種又は2種以上15%以
下、チタン、カルシウムの何れか1種又は2種10
%以下、硼素3%以下の何れか1種又は2種以上
の全量0.1〜50%を含有してなる合金に、 (A) 合金の融点以下250℃以上の温度で5分以上
100時間以下加熱して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 (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
熱して急冷するかあるいは毎秒1℃以下の速度
で徐冷する の順序の工程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−Co基吸振
合金の製造方法。[Scope of Claims] 1. Cobalt 0.1 to 20%, one or both of lead and antimony 50% or less, cerium 40% or less, tantalum 20% or less, iron, niobium, and zirconium in terms of weight ratio. Any one or more than 15%,
Damping capacity Q -1 with increased dislocation density, consisting of 10% or less of one or both of titanium and calcium, 3% or less of boron, a total amount of 0.1 to 50% of one or more of these, and the balance aluminum. An Al-Co-based vibration-absorbing alloy characterized in that the is 6×10 -3 or more. 2 By weight, 0.1 to 20% cobalt, 50% or less of one or two of lead and antimony, 40% or less of cerium, 20% or less of tantalum, and one or two of iron, niobium, and zirconium. More than species and less than 15%,
An alloy consisting of 10% or less of one or both of titanium and calcium, 3% or less of boron, a total amount of 0.1 to 50% of one or more of them, and the balance aluminum, (A) 250% below the melting point of the alloy. After heating at a temperature of 5 minutes or more and 100 hours or less at a temperature of 100°C or higher and cooling rapidly or gradually cooling at a rate of 1°C or less per second, (B) Attenuation ability Q - A method for producing an Al-Co-based vibration absorbing alloy, characterized in that 1 is 6×10 -3 or more. 3 In terms of weight ratio, an alloy consisting of 0.1 to 20% cobalt and the balance aluminum, with lead as a subcomponent,
50% or less of any one or both of antimony, 40% or less of cerium, 20% or less of tantalum, iron, niobium,
15% or less of any one or more of zirconium, one or more of titanium and calcium10
(A) At a temperature of 250°C or higher below the melting point of the alloy for 5 minutes or more.
After heating for 100 hours or less and rapidly cooling or slowly cooling at a rate of 1°C per second or less, (B) cold working with a cold working rate of 5% or more (C) (B) with a cold working rate of 5% or more Damping capacity Q -1 can be achieved by heating the processed material at a temperature of 250°C or less for 1 minute or more and 500 hours or less, and then rapidly cooling it, or slowly cooling it at a rate of 1°C or less per second. 6×
A method for producing an Al-Co-based vibration-absorbing alloy, characterized in that it has a vibration absorbing alloy of 10 -3 or more.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11276079A JPS5638441A (en) | 1979-09-05 | 1979-09-05 | A -co based vibration absorbing alloy and producing same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11276079A JPS5638441A (en) | 1979-09-05 | 1979-09-05 | A -co based vibration absorbing alloy and producing same |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2367787A Division JPS62188759A (en) | 1987-02-05 | 1987-02-05 | Al-co-base high-damping alloy and its production |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5638441A JPS5638441A (en) | 1981-04-13 |
| JPS6242984B2 true JPS6242984B2 (en) | 1987-09-10 |
Family
ID=14594841
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11276079A Granted JPS5638441A (en) | 1979-09-05 | 1979-09-05 | A -co based vibration absorbing alloy and producing same |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5638441A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5932461A (en) * | 1982-08-18 | 1984-02-21 | 渋谷工業株式会社 | Forcibly hermetically sealing and filling method and apparatus |
-
1979
- 1979-09-05 JP JP11276079A patent/JPS5638441A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5638441A (en) | 1981-04-13 |
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