JPS5843459B2 - Aluminum sintered alloy member and its manufacturing method - Google Patents
Aluminum sintered alloy member and its manufacturing methodInfo
- Publication number
- JPS5843459B2 JPS5843459B2 JP7752478A JP7752478A JPS5843459B2 JP S5843459 B2 JPS5843459 B2 JP S5843459B2 JP 7752478 A JP7752478 A JP 7752478A JP 7752478 A JP7752478 A JP 7752478A JP S5843459 B2 JPS5843459 B2 JP S5843459B2
- Authority
- JP
- Japan
- Prior art keywords
- powder
- aluminum
- sintered alloy
- weight
- sintered
- 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 title claims description 40
- 239000000956 alloy Substances 0.000 title claims description 40
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims description 23
- 229910052782 aluminium Inorganic materials 0.000 title claims description 18
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 claims description 16
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 12
- 150000001639 boron compounds Chemical class 0.000 claims description 11
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 10
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- 229910052802 copper Inorganic materials 0.000 claims description 8
- 239000010949 copper Substances 0.000 claims description 8
- 229910052749 magnesium Inorganic materials 0.000 claims description 8
- 239000011777 magnesium Substances 0.000 claims description 8
- 229910021538 borax Inorganic materials 0.000 claims description 6
- 235000010339 sodium tetraborate Nutrition 0.000 claims description 6
- 239000004328 sodium tetraborate Substances 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 5
- 229910021540 colemanite Inorganic materials 0.000 claims description 4
- 239000013078 crystal Substances 0.000 claims description 4
- UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 claims description 4
- 239000000843 powder Substances 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- 239000000314 lubricant Substances 0.000 claims description 2
- 239000011812 mixed powder Substances 0.000 claims description 2
- 239000011863 silicon-based powder Substances 0.000 claims description 2
- 238000005245 sintering Methods 0.000 description 13
- 229910052710 silicon Inorganic materials 0.000 description 9
- 239000010703 silicon Substances 0.000 description 9
- 230000000694 effects Effects 0.000 description 7
- 238000000465 moulding Methods 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 238000002425 crystallisation Methods 0.000 description 4
- 230000008025 crystallization Effects 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 241000209094 Oryza Species 0.000 description 3
- 235000007164 Oryza sativa Nutrition 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000009792 diffusion process Methods 0.000 description 3
- 235000009566 rice Nutrition 0.000 description 3
- 239000000654 additive Substances 0.000 description 2
- -1 boron sesquioxide Chemical class 0.000 description 2
- ZADPBFCGQRWHPN-UHFFFAOYSA-N boronic acid Chemical compound OBO ZADPBFCGQRWHPN-UHFFFAOYSA-N 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229910017639 MgSi Inorganic materials 0.000 description 1
- 229910017623 MgSi2 Inorganic materials 0.000 description 1
- MKYBYDHXWVHEJW-UHFFFAOYSA-N N-[1-oxo-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propan-2-yl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(C(C)NC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 MKYBYDHXWVHEJW-UHFFFAOYSA-N 0.000 description 1
- 229910003252 NaBO2 Inorganic materials 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000000573 anti-seizure effect Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000004320 controlled atmosphere Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910000765 intermetallic Inorganic materials 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- NVIFVTYDZMXWGX-UHFFFAOYSA-N sodium metaborate Chemical compound [Na+].[O-]B=O NVIFVTYDZMXWGX-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Powder Metallurgy (AREA)
Description
【発明の詳細な説明】
この発明は、アルミニウム焼結合金部材ならびにその製
造方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an aluminum sintered alloy member and a method for manufacturing the same.
従来、アルミニウムな主成分とした焼結合金は、耐蝕性
を有すること、軽量であることなどの利点がある反面、
機械的強度が十分でなくまた焼結条件の設定が比較的離
しいなどの問題があって、必ずしも満足すべき結果が得
られていない。Traditionally, sintered alloys with aluminum as the main component have advantages such as corrosion resistance and light weight.
There are problems such as insufficient mechanical strength and sintering conditions are set relatively far apart, and satisfactory results are not necessarily obtained.
この発明は、従来のこのような問題点を大巾に改善する
ことに成功したもので、とくに三二酸化はう素などのほ
う素化合物を配合することによって、焼結合金部材の機
械的強度が著しく高められ、しかも焼結合金を得るに当
って大気中にて焼結が可能であるという特徴を有するも
のである。This invention has succeeded in significantly improving these conventional problems. In particular, by incorporating a boron compound such as boron sesquioxide, the mechanical strength of the sintered alloy member can be improved. Moreover, the sintered alloy can be sintered in the atmosphere to obtain a sintered alloy.
すなわち、重量比で銅0.5〜6多、マグネシウム0.
2〜2宏けい素0.2〜2%、三二酸化はう素(B20
3)、四はう酸ソーダ(Na2B407)、以下焼結し
て結晶水を飛ばしたコレマナイト、パンデルミツト(い
ずれもCa2B、01、)、ポロナトロカルサイト(C
aB407・NaBO2)から選ばれた一種もしくは二
種以上を混合したほう素化合物0.5〜6%そして残部
アルミニウムからなるアルミニウム焼結合金部材ならび
に七0製造方法を提供するものである。That is, the weight ratio is 0.5-6% copper and 0.6% magnesium.
2-2 Hiroshi silicon 0.2-2%, boron sesquioxide (B20
3), Sodium tetraborate (Na2B407), colemanite which has been sintered to remove crystal water, pandermite (both Ca2B, 01), polonatrocalcite (C
The present invention provides an aluminum sintered alloy member consisting of 0.5 to 6% of a boron compound, which is a mixture of one or more selected from aB407 and NaBO2, and the balance aluminum, as well as a manufacturing method.
この発明でアルミニウム焼結合金部材とは、機械部品、
構造部材、治具、金具などをいい、すべりを主体とする
ような摺動部材は含まない。In this invention, the aluminum sintered alloy member refers to mechanical parts,
Refers to structural members, jigs, metal fittings, etc., and does not include sliding members that primarily slide.
本発明者らの実験によれば、とくに摺動部材として使用
される場合は、A l −Cu−Mg−8i系の焼結合
金においては、Si量が少くとも5重量φ以上でないと
、摺動部材としての耐焼付き性、耐荷重性が十分でなく
、はとんど実用に供し得ないことが確められている。According to experiments conducted by the present inventors, especially when used as a sliding member, in the case of Al-Cu-Mg-8i based sintered alloy, unless the amount of Si is at least 5 weight φ or more, sliding becomes difficult. It has been confirmed that the anti-seizure and load-bearing properties of this material as a moving member are insufficient, and it is almost impossible to put it into practical use.
この発明で、はう素化合物は三二酸はう素(B203)
、はう砂(Na2B407・10H20)、コレマナイ
ト(Ca2B601.−5H20)、パンデルミツト(
Ca2B601、・3H20)、ボロナトロカルサイト
(CaB407・NaBO2・6H20)などが使用さ
れるが、とくに三二酸化はう素、ついでほう砂が有効で
ある。In this invention, the boronate compound is boronate (B203)
, sand (Na2B407.10H20), colemanite (Ca2B601.-5H20), pandelmite (
Ca2B601, .3H20), boronatrocalcite (CaB407.NaBO2.6H20), etc. are used, but borium sesquioxide is particularly effective, followed by borax.
結晶水を含むほう酸塩を使用する場合は、結晶水を全部
飛ばしたものを使用することが重要である。When using borate containing water of crystallization, it is important to use one that has all the water of crystallization removed.
すなわち、たとえばほう砂(Na2B40710H20
)の場合は、これを400℃で焼いて結晶水を除去し、
四はう酸ソーダ(Na2B407)として使用する。That is, for example, borax (Na2B40710H20
), bake it at 400℃ to remove crystal water,
Used as sodium tetrabolate (Na2B407).
このように結晶水を含むものは、これを全部除去してか
ら使用しないと効果が現われない。Products that contain water of crystallization will not be effective unless all of this water is removed before use.
はう素化合物は、圧粉体の焼結性を向上せしめ、焼結合
金部材としての機械的強度を著しく向上せしめる効果が
ある。The boronic compound has the effect of improving the sinterability of the green compact and significantly improving the mechanical strength of the sintered alloy member.
本発明者の実験によれば、三二酸化はう素は0.5重量
饅前後の添加ですでに効果が現われ、2重量φ前後で機
械的強度向上にもつとも寄与し、無添加のものに比較し
て約2倍の強度上昇が確認された。According to the inventor's experiments, the effect of boron sesquioxide is already visible when it is added at around 0.5 weight φ, and it also contributes to improving mechanical strength at around 2 weight φ, compared to the one without additive. It was confirmed that the strength increased approximately twice as much.
2重量饅を超えてさらに多量に添加すると、強度は減少
し始め、10重重量前後の添加では無添加の合金と同程
度の強度となる。If a larger amount than 2 weights is added, the strength begins to decrease, and when around 10 weights is added, the strength becomes comparable to that of an alloy without additives.
上述したほう素化合物は、金属酸化物を溶解せしめる作
用があり、また圧粉体焼結時に成分の酸化を防止する効
果があるから、アルミニウム粉末の焼結性を向上せしめ
、とくに大気中においても焼結を可能ならしめるものと
考えられるが、さらに大きな効果は銅およびマグネシウ
ムおよびあるいはマグネシウムとけい素との化合物(M
gSi2)のアルミニウム中への拡散を助長し均一な合
金組成とすることで、本発明者はX線マイクロアナライ
ザーによる解析の効果、この事実を確認した。The boron compounds mentioned above have the effect of dissolving metal oxides and preventing the oxidation of the components during compact sintering, so they improve the sinterability of aluminum powder, especially in the atmosphere. It is thought that this makes sintering possible, but an even greater effect is due to the use of copper and magnesium, or compounds of magnesium and silicon (M
By promoting the diffusion of gSi2) into aluminum and creating a uniform alloy composition, the present inventor confirmed this fact and the effect of analysis using an X-ray microanalyzer.
すなわち、はう素化合物を添加しない合金においては、
たとえば銅成分は焼結合金中の粒界もしくはボイドの周
辺に多く分布するが、該化合物を添加することによって
銅の分布は著しく均一となり、アルミニウム中への拡散
が順調に進んでいることが確認された。In other words, in alloys that do not contain boronate compounds,
For example, the copper component is largely distributed around grain boundaries or voids in the sintered alloy, but by adding this compound, the distribution of copper becomes extremely uniform, confirming that the diffusion into the aluminum is proceeding smoothly. It was done.
したがって焼結体の合金化が高度にはかられ、焼結合金
部材としての強度が著しく向上したものと考えることが
できる。Therefore, it can be considered that the sintered body was highly alloyed and the strength as a sintered alloy member was significantly improved.
しかしこのほう素化合物の添加は焼結体の多孔度を増す
傾向にあり、とくに2重量φを超えて添加量を増すとこ
の傾向は著しい。However, the addition of this boron compound tends to increase the porosity of the sintered body, and this tendency is particularly significant when the amount added exceeds 2 weight φ.
前述したようにほう素化合物2重量優なピークとして強
度低下をきたすのは、焼結合金中の成分の拡散が進み、
合金化が高度にはかられるというメリットがある反面、
この多孔度増加にともなう強度の低下というデメリット
があって、この両者のバランスがくずれたからにほかな
らない。As mentioned above, the reason why the strength decreases as a peak with 2 weight predominant boron compounds is due to the progress of diffusion of components in the sintered alloy.
Although it has the advantage of being highly alloyed,
This increase in porosity has the disadvantage of a decrease in strength, and this is simply because the balance between the two has been disrupted.
焼結合金に潤滑油を會浸し、自己潤滑性を賦与せしめて
摺動部材として使用する場合は、合金の多孔度は重要な
要素であるが、この発明では多孔度は必要でない。When a sintered alloy is impregnated with lubricating oil to impart self-lubricating properties and is used as a sliding member, the porosity of the alloy is an important factor, but the present invention does not require porosity.
強度は可及的に高いことが望まれ、この観点からほう素
化合物は0.5〜6重量宏就中1〜4重量饅が望ましい
。It is desired that the strength is as high as possible, and from this point of view, the boron compound is desirably 1 to 4 weights out of 0.5 to 6 weights.
銅成分は、合金の強度向上に寄与するが、この発明では
0.5重量饅以下ではほとんど効果がなく、また6重量
饅を超えて添加すると、材質を脆くする傾向がでてくる
から、添加量はQ、5〜6重量袈とすることが望ましい
。The copper component contributes to improving the strength of the alloy, but in this invention, it has little effect if it is less than 0.5 weight, and if it is added in excess of 6 weight, it tends to make the material brittle. The amount is preferably Q, 5 to 6 weight kesa.
マグネシウム成分は、銅と共存して合金の機械的強度向
上に寄与するほか、一部けい素とMgSi2の形で拡散
しアルミニウム焼結合金の時効硬化性に寄与する。The magnesium component not only coexists with copper and contributes to improving the mechanical strength of the alloy, but also partially diffuses in the form of silicon and MgSi2 and contributes to the age hardenability of the aluminum sintered alloy.
この発明では、0.2重量饅以下ではほとんど効果がな
く、また2重量饅を超えて添加すると反って強度低下を
きたし、また焼結性も悪くなる。In this invention, if less than 0.2 weight of rice cake is added, there is almost no effect, and if it is added in excess of 2 weight of rice cake, it will warp, resulting in a decrease in strength, and the sinterability will also deteriorate.
したがってマグネシウムは0.2〜2重量優とすること
が望ましい。Therefore, it is desirable that the amount of magnesium be 0.2 to 2% by weight.
けい素はアルミニウム中に不純物として含まれるが、多
くても2重量優までとする。Silicon is contained in aluminum as an impurity, but it is limited to more than 2 parts by weight at most.
就中0.2〜0.8重量φであることが望ましい。In particular, it is desirable that the weight φ is 0.2 to 0.8.
すでに述べたように、けい素はマグネシウムとMgSi
2の形の金属間化合物を作り、こ益がアルミニウム焼結
合金の時効硬化性に寄与するが、大部分は合金中でけい
素のままの形で分散して存在する。As already mentioned, silicon is magnesium and MgSi
Silicon forms an intermetallic compound of type 2, which contributes to the age hardenability of the aluminum sintered alloy, but most of the silicon exists in the alloy in the form of a dispersed silicon.
したがって合金の均質性を損い易いので、耐焼付き性な
どを要求される摺動部材として使用するのでない限り、
けい素を多量に分散せしめることは有益ではない。Therefore, it is easy to damage the homogeneity of the alloy, so unless it is used as a sliding member that requires seizure resistance, etc.
It is not beneficial to disperse silicon in large amounts.
上述した成分組成からなるこの発明の焼結合金部材を得
るに際し、成形圧力は1〜6トン/cd、就中2〜5ト
ン/cdが適当である。When obtaining the sintered alloy member of the present invention having the above-mentioned composition, a suitable molding pressure is 1 to 6 tons/cd, particularly 2 to 5 tons/cd.
成形圧力が2トン/cdで理論密度比90%を超える。When the molding pressure is 2 tons/cd, the theoretical density ratio exceeds 90%.
焼結温度は550〜640℃とアルミニウムの融点以下
の@度とし、焼結時間は5〜60分間とすることが適当
である。It is appropriate that the sintering temperature is 550 to 640°C, which is below the melting point of aluminum, and the sintering time is 5 to 60 minutes.
焼結雰囲気は中性もしくは還元性でもよいが、この発明
の特徴は大気中における焼結が可能なことで、しかも得
られた焼結体の機械的強度は雰囲気の相違によって何ん
ら著しい差が認められないということである。The sintering atmosphere may be neutral or reducing, but the feature of this invention is that sintering can be performed in the air, and there is no significant difference in the mechanical strength of the obtained sintered body depending on the atmosphere. This means that it is not recognized.
そしてほう素化合物を含まない焼結合金に比較して著し
く強度が太きいということである。Moreover, the strength is significantly higher than that of sintered alloys that do not contain boron compounds.
大気中焼結においては、焼結時間を過大にとることは何
んら益がない。In air sintering, there is no benefit in taking too long a sintering time.
前述した所定の温度に調整された炉内で迅速に焼結を進
めることが望ましく、焼結時間は30分間前後で焼結体
の機械的強度はほぼ最高強度に達する。It is desirable to proceed with the sintering quickly in a furnace adjusted to the predetermined temperature mentioned above, and the mechanical strength of the sintered body reaches approximately the maximum strength after sintering time of about 30 minutes.
そして得られた焼結体の外表面も雰囲気調整のもとに焼
結を行なったものと比較してほとんど遜色がない。The outer surface of the obtained sintered body is almost comparable to that of one sintered under controlled atmosphere.
このように重量比で銅0,5〜6%、マグネシウム0.
2〜2宏けい素0.2〜2宏はう素化合物0.5〜6%
、残部アルミニウムからなる焼結合金部材は機械的強度
が著しく高められ、機械部品、構造部品などの用途に最
適である。In this way, the weight ratio is 0.5 to 6% copper and 0.5% magnesium.
2-2 Hiroshi Silicon 0.2-2 Hiroshi Boron Compound 0.5-6%
The mechanical strength of the sintered alloy member, which is made of aluminum with the remainder being aluminum, has significantly increased mechanical strength, making it ideal for applications such as mechanical parts and structural parts.
とくに成分中のほう素化合物は、単に焼結性の向上、機
械的強度の向上にとどまらず、焼結合金の時効硬化性に
も寄与し、一層高強度の焼結合金部材とするものである
。In particular, the boron compound in the component not only improves sinterability and mechanical strength, but also contributes to the age hardenability of the sintered alloy, making the sintered alloy member even stronger. .
以下二三の実施例について説明する。A few examples will be described below.
実施例 1
200メツシユを通過する電解銅粉末4重量φ、同じく
200メツシユを通過するマグネシウム粉末0.5重量
饅、250メツシユを通過するけい素粉末0.8重量饅
、200メツシユを通過する三二酸化はう素2重量饅、
そして残部を250メツシユを通過するアトマイズアル
ミニウム粉末とし、これに少量のラウリルアルコール等
の滑剤(合金粉末100重量部に対して2重量部)を均
一に混合し、得られた混合粉末を金型中で成形圧力4ト
ン/cdで圧粉したのち金型から取出し、これを大気中
で580±10℃の温度で10分間焼成した。Example 1 4 weight φ of electrolytic copper powder passing through 200 meshes, 0.5 weight cup of magnesium powder passing through 200 meshes, 0.8 weight cup of silicon powder passing through 250 meshes, and sesquioxide passing through 200 meshes 2 weight rice cake with borosin,
The remainder is atomized aluminum powder that passes through 250 meshes, and a small amount of lubricant such as lauryl alcohol (2 parts by weight per 100 parts by weight of alloy powder) is uniformly mixed with this, and the resulting mixed powder is placed in a mold. After compacting at a molding pressure of 4 tons/cd, the powder was removed from the mold and fired in the atmosphere at a temperature of 580±10° C. for 10 minutes.
ついで、このようにして得た焼結合金をつぎの温度条件
で熱処理した。The sintered alloy thus obtained was then heat treated under the following temperature conditions.
イ)505±5°Cで30分間保持後 口)水冷し、 ハ)160±5°Cで18時間保持したのち放冷。b) After holding at 505±5°C for 30 minutes mouth) water cooling, c) After keeping at 160±5°C for 18 hours, let it cool.
実施例 ■
実施例■において成形圧力を6トン/cdとし、以下同
様にして焼結合金を得た。Example 2 A sintered alloy was obtained in the same manner as in Example 2 except that the molding pressure was 6 tons/cd.
ついでこれを実施例■と同様の温度条件で熱処理した。This was then heat treated under the same temperature conditions as in Example (2).
実施例 ■
実施例■において、三二酸化ホウ素の代りには5砂を4
00°Cで焼いて結晶水を完全に飛ばして得た四はう酸
ソーダ(Na2B40□ )粉末を用い、以下同様にし
て焼結合金を得た。Example ■ In Example ■, 5 sand was used instead of boron sesquioxide.
A sintered alloy was obtained in the same manner using sodium tetraborate (Na2B40□) powder obtained by baking at 00°C to completely remove crystallization water.
ついで、これを実施例■と同様の温度条件で熱処理した
。This was then heat-treated under the same temperature conditions as in Example (2).
比較例 1
実施例■において、三二酸化はう素を加えることなく残
部をアルミニウム粉末とし、以下同様にして焼結合金を
得た。Comparative Example 1 A sintered alloy was obtained in the same manner as in Example (2) except that boron sesquioxide was not added and the remainder was aluminum powder.
ついで、これを実施例■と同様の温度条件で熱処理した
。This was then heat-treated under the same temperature conditions as in Example (2).
比較例 2
実施例■において三二酸化はう素を加えることなく、残
部をアルミニウム粉末とし、かつ成形圧力を6トン/c
rAとして以下同様に焼結合金を得た。Comparative Example 2 In Example ■, no boron sesquioxide was added, the remainder was aluminum powder, and the molding pressure was 6 tons/c.
A sintered alloy was obtained as rA in the same manner as below.
ついで、これを実施例■と同様の温度条件で熱処理した
。This was then heat-treated under the same temperature conditions as in Example (2).
表は以上の各実施例、比較例による焼結合金の機械的強
度を示すものである。The table shows the mechanical strength of the sintered alloys according to each of the above examples and comparative examples.
上表から実施例■乃至実施例■からなるアルミニウム焼
結合金部材の機械的強度は比較例1乃至比較例2と比べ
て著しく高められていることがわかる。From the above table, it can be seen that the mechanical strength of the aluminum sintered alloy members of Examples 1 and 2 is significantly increased compared to Comparative Examples 1 and 2.
なお、焼結合金部材の使用目的によっては上述した実施
例における方法以外に、圧粉体を金型中で加圧しながら
加熱するという焼結方法を採用することにより、さらに
高密度、高強度の焼結合金部材を得ることができる。Depending on the intended use of the sintered alloy member, a sintering method in which the green compact is heated while being pressurized in a mold, in addition to the method described in the above embodiment, may be used to achieve even higher density and higher strength. A sintered metal member can be obtained.
なお使用目的によっては、金型中で加圧しながら、加熱
するという焼結方法を採用することによリ、
さらに高密度、高強度の焼結合金部材を得ることができ
る。Depending on the purpose of use, a sintered alloy member with even higher density and higher strength can be obtained by adopting a sintering method of heating while pressurizing in a mold.
Claims (1)
宏けい素0.2〜2係、三二酸化はう素、四はう酸ソー
ダ、以下焼成して結晶水を飛ばしたコレマナイト、パン
デルミツト、ボロナトロカルサイトから選ばれた一種も
しくは二種以上を混合したほう素化合物0.5〜6φ、
そして残部アルミニウムからなることを特徴とした機械
部品、構造部材用アルミニウム焼結金部材。 2 重量比で銅粉末0.5〜6%、マグネシウム粉末0
.2〜2%、けい素粉末0.2〜2%、三二酸化はう素
、四はう酸ソーダ、以下焼成して結晶水を飛ばしたコレ
マナイト、パンデルミツト、ボロナトロカルサイトから
選ばれた一種もしくは二種以上を混合したほう素化合物
粉末0.5〜6%、そして残部アルミニウム粉末を少量
の滑剤とともに均一に混合し、得られた混合粉末を成形
圧力1〜6トン/cdで圧粉成形したのち、該成形物を
550〜640℃の温度で5〜60分間焼結することを
特徴とした機械部品、構造部材用アルミニウム焼結合金
部材の製造方法。[Claims] 1. Copper 0.5-6%, magnesium 0.2-2% by weight
A mixture of one or more selected from the group consisting of 0.2 to 2% borosilicon, boron sesquioxide, sodium tetraborate, colemanite, pandermite, and boronatrocalcite which have been calcined to remove crystal water. boron compound 0.5~6φ,
And an aluminum sintered metal member for mechanical parts and structural members, characterized in that the remainder is made of aluminum. 2 Copper powder 0.5-6% by weight, magnesium powder 0
.. 2% to 2%, silicon powder 0.2% to 2%, boron sesquioxide, sodium tetraborate, a type selected from colemanite, pandermite, and boronatrocalcite, which have been calcined to remove crystal water, or 0.5-6% boron compound powder, which is a mixture of two or more types, and the balance aluminum powder were uniformly mixed together with a small amount of lubricant, and the obtained mixed powder was compacted at a compacting pressure of 1-6 tons/cd. A method for producing an aluminum sintered alloy member for mechanical parts and structural members, characterized in that the molded product is then sintered at a temperature of 550 to 640°C for 5 to 60 minutes.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7752478A JPS5843459B2 (en) | 1978-06-28 | 1978-06-28 | Aluminum sintered alloy member and its manufacturing method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7752478A JPS5843459B2 (en) | 1978-06-28 | 1978-06-28 | Aluminum sintered alloy member and its manufacturing method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS556438A JPS556438A (en) | 1980-01-17 |
| JPS5843459B2 true JPS5843459B2 (en) | 1983-09-27 |
Family
ID=13636350
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP7752478A Expired JPS5843459B2 (en) | 1978-06-28 | 1978-06-28 | Aluminum sintered alloy member and its manufacturing method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5843459B2 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62122813U (en) * | 1986-01-24 | 1987-08-04 | ||
| JPS63158928U (en) * | 1987-04-01 | 1988-10-18 |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6261336B1 (en) * | 2000-08-01 | 2001-07-17 | Rutgers, The State University Of New Jersey | Stable aqueous iron based feedstock formulation for injection molding |
| CN109735733B (en) * | 2019-03-06 | 2020-02-07 | 中国工程物理研究院材料研究所 | Special composite slag removing agent for refining beryllium-aluminum alloy, preparation method and slag removing method |
-
1978
- 1978-06-28 JP JP7752478A patent/JPS5843459B2/en not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62122813U (en) * | 1986-01-24 | 1987-08-04 | ||
| JPS63158928U (en) * | 1987-04-01 | 1988-10-18 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS556438A (en) | 1980-01-17 |
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