JPH01247538A - Manufacture of sliding material - Google Patents
Manufacture of sliding materialInfo
- Publication number
- JPH01247538A JPH01247538A JP63074709A JP7470988A JPH01247538A JP H01247538 A JPH01247538 A JP H01247538A JP 63074709 A JP63074709 A JP 63074709A JP 7470988 A JP7470988 A JP 7470988A JP H01247538 A JPH01247538 A JP H01247538A
- Authority
- JP
- Japan
- Prior art keywords
- powder
- binder
- powders
- alloy
- organic
- 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.)
- Pending
Links
- 239000000463 material Substances 0.000 title claims abstract description 25
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 14
- 239000000843 powder Substances 0.000 claims abstract description 64
- 239000011230 binding agent Substances 0.000 claims abstract description 20
- 229910052718 tin Inorganic materials 0.000 claims abstract description 12
- 229910052797 bismuth Inorganic materials 0.000 claims abstract description 10
- 229910052738 indium Inorganic materials 0.000 claims abstract description 6
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 5
- 229910010272 inorganic material Inorganic materials 0.000 claims abstract description 3
- 239000011147 inorganic material Substances 0.000 claims abstract description 3
- 239000011368 organic material Substances 0.000 claims abstract description 3
- 239000000956 alloy Substances 0.000 claims description 8
- 229910045601 alloy Inorganic materials 0.000 claims description 7
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 2
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims description 2
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 claims description 2
- 238000000034 method Methods 0.000 abstract description 17
- 230000001050 lubricating effect Effects 0.000 abstract description 16
- 238000002156 mixing Methods 0.000 abstract description 12
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract description 11
- 239000010953 base metal Substances 0.000 abstract description 11
- 238000005245 sintering Methods 0.000 abstract description 11
- 229910052745 lead Inorganic materials 0.000 abstract description 8
- 239000011247 coating layer Substances 0.000 abstract description 7
- 239000000203 mixture Substances 0.000 abstract description 5
- 239000004372 Polyvinyl alcohol Substances 0.000 abstract description 3
- 239000004115 Sodium Silicate Substances 0.000 abstract description 3
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 abstract description 3
- 229910052911 sodium silicate Inorganic materials 0.000 abstract description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 2
- 235000021355 Stearic acid Nutrition 0.000 abstract description 2
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 abstract description 2
- 239000008119 colloidal silica Substances 0.000 abstract description 2
- 239000010439 graphite Substances 0.000 abstract description 2
- 229910002804 graphite Inorganic materials 0.000 abstract description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 abstract description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 abstract description 2
- 239000008279 sol Substances 0.000 abstract description 2
- 239000008117 stearic acid Substances 0.000 abstract description 2
- 229910000838 Al alloy Inorganic materials 0.000 abstract 2
- 239000000654 additive Substances 0.000 abstract 1
- 230000000996 additive effect Effects 0.000 abstract 1
- 238000013019 agitation Methods 0.000 abstract 1
- 230000010354 integration Effects 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 125000000914 phenoxymethylpenicillanyl group Chemical group CC1(S[C@H]2N([C@H]1C(=O)*)C([C@H]2NC(COC2=CC=CC=C2)=O)=O)C 0.000 abstract 1
- 239000002245 particle Substances 0.000 description 9
- 239000000314 lubricant Substances 0.000 description 7
- 238000009826 distribution Methods 0.000 description 6
- 230000005484 gravity Effects 0.000 description 5
- 229910000978 Pb alloy Inorganic materials 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 238000005266 casting Methods 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 229910001020 Au alloy Inorganic materials 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003353 gold alloy Substances 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 238000009828 non-uniform distribution Methods 0.000 description 1
- 238000005204 segregation Methods 0.000 description 1
Landscapes
- Powder Metallurgy (AREA)
Abstract
Description
【発明の詳細な説明】
〔発明の目的〕
(産業上の利用分野)
本発明は軸受材料等の摺動用材料を製造する方法に係り
、特にアルミニウムまたはその合金からなる基体金属中
に重量金属からなる潤滑成分を含ませる摺動用材料の製
造方法に関する。[Detailed Description of the Invention] [Objective of the Invention] (Industrial Field of Application) The present invention relates to a method for manufacturing sliding materials such as bearing materials, and in particular, the present invention relates to a method for manufacturing sliding materials such as bearing materials. The present invention relates to a method for producing a sliding material containing a lubricating component.
(従来の技術)
軸受等に用いるアルミニウム(Aオ)系の摺動用材料と
して、スズ(Sn)、鉛(Pb)、ビスマス(Bi)、
インジウム(In)等の重量金属からなる潤滑成分を含
むものが知られている。(Prior art) Aluminum (A)-based sliding materials used in bearings, etc. include tin (Sn), lead (Pb), bismuth (Bi),
Those containing a lubricating component made of a heavy metal such as indium (In) are known.
従来、このような摺動用材料の製造方法としては鋳造法
が主流であった。しかし、基体金属としてのAIと、3
n、pb、3i、in等ノrjJ酒成分とは比重差が大
きく、重着偏析が生じ易いため、この鋳造法では潤滑成
分の添加量が多い材料の製造は困難であり、添加量の少
ない材料の製造に限られている。Conventionally, casting has been the mainstream method for manufacturing such sliding materials. However, with AI as the base metal, 3
There is a large difference in specific gravity from alcohol components such as n, pb, 3i, in, etc., and heavy segregation tends to occur, so it is difficult to manufacture materials with a large amount of lubricant added using this casting method, and it is difficult to produce materials with a large amount of lubricant added. Limited to the manufacture of materials.
そこで、潤滑成分添加量を増大する方法として粉末焼結
法が試みられている。粉末焼結法では基体金属としての
Aオの粉末と潤滑成分としてのSn、Pb、Bi、In
等の粉末とを混合、攪拌した模、焼結して一体化する方
法で、鋳造法よりも大量の潤滑成分の添加が可能である
。Therefore, a powder sintering method has been attempted as a method of increasing the amount of lubricant added. In the powder sintering method, A powder as a base metal and Sn, Pb, Bi, In as lubricating components are used.
This method involves mixing, stirring, and sintering powders such as powders, etc., and then sintering them to form a single body.It is possible to add a larger amount of lubricating components than with the casting method.
(発明が解決しようとする課題)
ところが、粉末焼結法においても、粉末混合過程で比重
差により潤滑成分の偏在が起こり、軸受等に望まれる十
分高い添加量を得ることが困難であった。(Problems to be Solved by the Invention) However, even in the powder sintering method, uneven distribution of lubricating components occurs due to differences in specific gravity during the powder mixing process, making it difficult to obtain a sufficiently high addition amount desired for bearings and the like.
本発明はこのような事情に鑑みてなされたもので、粉末
焼結法により、潤滑成分の偏在を生じることなく十分高
い添加量が容易に、かつ自由調整可能な状態で得ること
ができる摺動用材料の製造方法を捏供することを目的と
する。The present invention was made in view of the above circumstances, and is a sliding material that can easily and freely adjust a sufficiently high amount of lubricating components without causing uneven distribution of the lubricating components by a powder sintering method. The purpose is to provide information on manufacturing methods for materials.
(課題を解決するための手段と作用)
本発明は、AIまたはその合金の粉末と、Sn、Pb、
Biおよびinから選択されるいずれか1種または2種
以上の粉末とを、有機または無機材料からなるバインダ
とともに混合、攪拌した後、焼結して一体化することを
¥f@とする。(Means and effects for solving the problems) The present invention provides powders of AI or its alloys, Sn, Pb,
¥f@ refers to mixing and stirring one or more powders selected from Bi and in with a binder made of an organic or inorganic material, and then sintering and integrating the powder.
このような本発明は以下の知見に基づいてなされたもの
である。即ち、基体金属としてのAIまたはA1合金の
粉末と、潤滑成分としてのSn。The present invention has been made based on the following findings. That is, powder of AI or A1 alloy as a base metal and Sn as a lubricating component.
pb、3iまたはtnの粉末とは、そのままの状態では
粉末同士の界面で滑り易く、重量差によって攪拌混合時
に上下に偏在分離する。特に基体金属の含有率が高い関
標上、AIまたはへ1合金粉末の粒径を大きくし、Sn
、Pb、Bi、In等の粉末の粒径を小さくして混合し
た場合、重1が大きく粒径の小さいSn、pb、Bi、
in等の粉末はへlまたはAI金合金粉末間隙間を介し
て落下して下部に集積し、上部にはAIまたは1合金の
みが存在づる状態となり易い。Pb, 3i, or tn powders tend to slip on the interface between the powders in their original state, and due to the difference in weight, they are unevenly separated vertically during stirring and mixing. In particular, since the content of the base metal is high, the particle size of AI or He1 alloy powder is increased, and Sn
, Pb, Bi, In, etc., when the particle size is reduced and mixed, the weight 1 is large and the particle size is small, such as Sn, pb, Bi,
In and other powders fall through the gaps between the aluminum or AI gold alloy powders and accumulate in the lower part, and only AI or one alloy tends to exist in the upper part.
そこで、粉末の界面に接着性を与えれば、重量粉末の落
下動作が抑Mされ、重量粉末の下部偏在が防止できるも
のと考えられ、本発明では基体金属粉末とrA潤滑成分
粉末とを有機または無機のバインダとともに混合、攪拌
することにより、その粉末表面にバインダの被膜層を形
成するものである。このバインダにより、例えば粒径の
大きいAIまたはA7合金の表面に、微細なSn、Pb
。Therefore, it is believed that if adhesiveness is imparted to the powder interface, the falling movement of the heavy powder can be suppressed and the uneven distribution of the heavy powder at the bottom can be prevented.In the present invention, the base metal powder and the rA lubricating component powder are By mixing and stirring with an inorganic binder, a binder coating layer is formed on the powder surface. With this binder, for example, fine Sn, Pb
.
3i、ln等の粉末が付着する状態となり、粉末全体と
して均一な混合状態が維持される。即ち、混合過程で比
重の差により重量のあるSn、Pb。The powders such as 3i and ln adhere to each other, and a uniform mixed state is maintained as a whole. That is, Sn and Pb are heavier due to the difference in specific gravity during the mixing process.
3i、in等の粉末が一部に偏在することが防止でき、
または大幅に抑v1できる。It is possible to prevent powders such as 3i and in from being unevenly distributed in some areas,
Or it can be significantly suppressed by v1.
バインダは、焼結前の粉末混合時に偏在することを防止
できればよく、有機または無機の種々のバインダを適用
できる。The binder only needs to be able to prevent uneven distribution during powder mixing before sintering, and various organic or inorganic binders can be used.
有機バインダとしては、例えばポリビニルアルコール(
PVA)、ステアリン酸、リン酸アルミニウム等が適用
できる。Examples of organic binders include polyvinyl alcohol (
PVA), stearic acid, aluminum phosphate, etc. can be applied.
また、無機バインダとしては、例えばアルミナゾル、ケ
イ酸ソーダ、黒鉛、コロイダルシリカ等が適用できる。Further, as the inorganic binder, for example, alumina sol, sodium silicate, graphite, colloidal silica, etc. can be used.
なお、アルミナゾルは乾燥により結晶化して、強固な粉
末結合作用を呈することから、本発明で用いるバインダ
として好適である。Note that alumina sol is suitable as the binder used in the present invention because it crystallizes upon drying and exhibits a strong powder binding effect.
バインダを添加した粉末は、予備乾燥(アルミナゾルの
場合は150℃で数時間乾燥)を行ない、または直接に
金型に充填して焼結する。これにより、潤滑成分が均一
に分散した高品質の軸受材料等を、そのrIJ滑成分成
分添加量いものとして、また自由なコントロールのもと
で得られるようになる。The binder-added powder is pre-dried (in the case of alumina sol, dried at 150° C. for several hours) or directly filled into a mold and sintered. This makes it possible to obtain high-quality bearing materials in which the lubricating components are uniformly dispersed, with the added amount of the rIJ lubricating components being freely controlled.
本発明の方法により得られるm肋材料は、軸受のほか、
回転または平行動作用の各種摺動用部材として広く適用
することができる。The m rib material obtained by the method of the present invention can be used not only for bearings but also for bearings.
It can be widely applied as various sliding members for rotating or parallel action.
(実施例)
基体金属としての平均粒径が40μ■のA1粉末(99
,7wt%AJ)と、潤滑成分としての平均粒径が5μ
mのpb粗粉末を、重量比85:15で混合し、これに
その総酸の15wt%の割合でバインダとしてのアルミ
ナゾル(アルミナ水和物含有1110wt%)を添加し
、約30分間攪拌した。これにより、AI粉末およびp
b粗粉末表面に均一なアルミナゾルの被膜層が形成され
た。(Example) A1 powder (99
, 7wt%AJ) and an average particle size of 5μ as a lubricant component.
m of Pb coarse powder were mixed at a weight ratio of 85:15, and alumina sol (containing alumina hydrate: 1110 wt%) as a binder was added thereto at a ratio of 15 wt% of the total acid, and stirred for about 30 minutes. This allows AI powder and p
b A uniform coating layer of alumina sol was formed on the surface of the coarse powder.
第1図(A)はこのようなアルミナゾル被膜層が形成さ
れたΔl粉末とpb粗粉末の混合状態を示すものである
。同図に示すように、粒径の大きいAI粉末の表面にア
ルミナゾルの被膜層を介して粒径の小さいpb粗粉末均
一に分散重着した状態が得られた。即ち、AIとPbと
の比重差による重力偏在が生じることはなく、pb粗粉
末上下均一に分散した。FIG. 1(A) shows a mixed state of Δl powder and PB coarse powder on which such an alumina sol coating layer is formed. As shown in the figure, a state was obtained in which coarse Pb powder with small particle size was uniformly dispersed and deposited on the surface of AI powder with large particle size via a coating layer of alumina sol. That is, uneven distribution of gravity due to the difference in specific gravity between AI and Pb did not occur, and the coarse Pb powder was evenly dispersed above and below.
このようなA1.Pb粉末混合体を約2時間、150℃
に加熱した侵、大気中で乾燥させた。これにより、アル
ミナゾルの被膜層がゲル化して、AJ粉末とpb粉末と
の間の接合力がさらに向上し、途中の製造工程で再び分
離することはなかった。Such A1. Pb powder mixture was heated at 150°C for about 2 hours.
The sample was heated to a temperature of 100 mL and dried in air. As a result, the coating layer of alumina sol gelled, and the bonding force between the AJ powder and the PB powder was further improved, and they did not separate again during the manufacturing process.
その後、乾燥したA1.Pb粉末混合体を金型内に充填
して、500℃で約30分間の焼結成形を行なった。こ
の結果、第1図(B)に示すように、基体金属としての
AI中にpbが均一に分散したAJ−Pb合金軸受材料
が得られた。After that, the dried A1. A mold was filled with the Pb powder mixture, and sintering was performed at 500° C. for about 30 minutes. As a result, as shown in FIG. 1(B), an AJ-Pb alloy bearing material was obtained in which Pb was uniformly dispersed in AI as the base metal.
なお、バインダとしてアルミナゾルのほか、有機、無機
のバインダ、例えばケイ酸ソーダを使用した場合にも前
記同様にpbが均一に分散したAJ−Pb合金軸受材料
が得られた。In addition, when an organic or inorganic binder such as sodium silicate was used in addition to alumina sol as the binder, an AJ-Pb alloy bearing material in which Pb was uniformly dispersed was obtained in the same manner as described above.
また、基体金属としてA7合金を用い、あるいは摺動成
分としてpb粉末単体のほか、Sn、Bi、lnの粉末
単体またはこれらの2種以上の粉末を用いた場合にも、
これらの摺動成分が均一に分散することが認められた。In addition, when A7 alloy is used as the base metal, or when using PB powder alone, Sn, Bi, or ln powder alone or two or more of these powders as the sliding component,
It was observed that these sliding components were uniformly dispersed.
さらに、粒径を種々変更した場合にも、前記と略同様に
摺動成分の均一な分散状態が得られることが認められた
。Furthermore, even when the particle size was varied, it was found that the sliding component could be uniformly dispersed in substantially the same manner as described above.
(従来例)
前記実施例と同様のAオ粉末(平均粒径40um、99
.7wt%J611)と、pb粉末(平均粒径5μm)
とを、重量比85:15でバインダを用いることなく混
合し、約30分間攪拌した。(Conventional example) A powder similar to the above example (average particle size 40 um, 99
.. 7 wt% J611) and pb powder (average particle size 5 μm)
were mixed at a weight ratio of 85:15 without using a binder, and stirred for about 30 minutes.
第2図(A)はこのようなAI粉末とpb粉末との混合
状態を示すものである。同図に示すように、pb粉末が
下方に偏在し、不均一な潤滑成分の分散状態となった。FIG. 2(A) shows a mixed state of such AI powder and PB powder. As shown in the figure, the PB powder was unevenly distributed downward, resulting in a non-uniform dispersion of the lubricant component.
これはAJとpbとの重量差によりpb粉末が混合過程
で落下し、下方に集積したものと考えられる。This is considered to be because the Pb powder fell during the mixing process due to the difference in weight between AJ and Pb and accumulated at the bottom.
このようなAI、Pb合金粉末混合体を金型内に充填し
て、前記実施例と同様に500℃で約30分間焼結成形
したところ、第2図(B)に示すように、基体金属とし
てのAIの下部にPbが多量に偏在した不均一分布状態
のAオーPb合金材料となった。When this AI and Pb alloy powder mixture was filled into a mold and sintered at 500°C for about 30 minutes in the same manner as in the previous example, as shown in Figure 2 (B), the base metal The result was an A-Pb alloy material with a non-uniform distribution in which a large amount of Pb was unevenly distributed under the AI.
以上のように本発明によれば、基体金属としてのAIま
たはその合金の粉末に、それよりも重量の大きい潤滑成
分としてのSn、Pb、Bi。As described above, according to the present invention, Sn, Pb, and Bi are added to the powder of AI or its alloy as the base metal and as lubricating components that are heavier than the base metal.
Inの1種または2種以上の粉末を加えて焼結法により
摺動材料を製造する場合、予め粉末表面にバインダの被
膜層を形成することによって粉末混合時のm清成分の偏
在を防止することができ、潤滑成分が従来に比して多量
に、かつ均一に分散混合した焼結摺動材料を自由な成分
コントロールが可能な状態で得られるという効果が奏さ
れる。When manufacturing a sliding material by a sintering method by adding one or more types of In powder, uneven distribution of m-tiny components during powder mixing is prevented by forming a binder coating layer on the powder surface in advance. This has the effect that a sintered sliding material in which lubricating components are dispersed and mixed in a larger amount and more uniformly than in the past can be obtained in a state where the components can be freely controlled.
第1図(A)は本発明の一実施例による製造途中状態の
粉末混合状態を示す模式図、第1図(B)は前記実施例
により製造されたM肋材料のra滑酸成分分散状態示す
模式図、第2図(A)は従来例による製造途中状態の粉
末混合状態を示す模式図、第2図(B)は従来例により
製造された摺動材料の潤滑成分分数状態を示す模式図で
ある。
(A) (B)第
1図
(Al (81第
2図FIG. 1(A) is a schematic diagram showing a state of powder mixing in the middle of production according to an embodiment of the present invention, and FIG. 1(B) is a state of dispersion of RA lubricant components in the M rib material produced according to the above embodiment. FIG. 2(A) is a schematic diagram showing the state of powder mixing in the middle of production according to the conventional example, and FIG. 2(B) is a schematic diagram showing the state of the lubricant component fraction of the sliding material manufactured according to the conventional example. It is a diagram. (A) (B) Figure 1 (Al (81 Figure 2)
Claims (1)
マスおよびインジウムから選択されるいずれか1種また
は2種以上の粉末とを、有機または無機材料からなるバ
インダとともに混合、攪拌した後、焼結して一体化する
ことを特徴とする摺動用材料の製造方法。A powder of aluminum or its alloy and one or more powders selected from tin, lead, bismuth and indium are mixed and stirred with a binder made of an organic or inorganic material, and then sintered. A method of manufacturing a sliding material characterized by integrating the sliding material.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63074709A JPH01247538A (en) | 1988-03-30 | 1988-03-30 | Manufacture of sliding material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63074709A JPH01247538A (en) | 1988-03-30 | 1988-03-30 | Manufacture of sliding material |
Publications (1)
Publication Number | Publication Date |
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JPH01247538A true JPH01247538A (en) | 1989-10-03 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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JP63074709A Pending JPH01247538A (en) | 1988-03-30 | 1988-03-30 | Manufacture of sliding material |
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JP (1) | JPH01247538A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996020043A1 (en) * | 1994-12-27 | 1996-07-04 | Basf Aktiengesellschaft | Method of producing a hydrogenation catalyser |
CN101967586A (en) * | 2010-11-12 | 2011-02-09 | 哈尔滨工业大学 | Method for preparing self-lubricating radiation-proof Al-Bi alloy |
-
1988
- 1988-03-30 JP JP63074709A patent/JPH01247538A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996020043A1 (en) * | 1994-12-27 | 1996-07-04 | Basf Aktiengesellschaft | Method of producing a hydrogenation catalyser |
CN101967586A (en) * | 2010-11-12 | 2011-02-09 | 哈尔滨工业大学 | Method for preparing self-lubricating radiation-proof Al-Bi alloy |
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