JPH04320497A - Self-lubricating composite material and its preparation - Google Patents
Self-lubricating composite material and its preparationInfo
- Publication number
- JPH04320497A JPH04320497A JP8692291A JP8692291A JPH04320497A JP H04320497 A JPH04320497 A JP H04320497A JP 8692291 A JP8692291 A JP 8692291A JP 8692291 A JP8692291 A JP 8692291A JP H04320497 A JPH04320497 A JP H04320497A
- Authority
- JP
- Japan
- Prior art keywords
- lubricating
- self
- composite material
- phase
- graphite
- 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.)
- Withdrawn
Links
- 239000002131 composite material Substances 0.000 title claims abstract description 20
- 229910045601 alloy Inorganic materials 0.000 claims abstract description 37
- 239000000956 alloy Substances 0.000 claims abstract description 37
- 230000001050 lubricating effect Effects 0.000 claims abstract description 30
- 239000000463 material Substances 0.000 claims abstract description 24
- 229910052751 metal Inorganic materials 0.000 claims abstract description 23
- 239000002184 metal Substances 0.000 claims abstract description 23
- ITRNXVSDJBHYNJ-UHFFFAOYSA-N tungsten disulfide Chemical compound S=[W]=S ITRNXVSDJBHYNJ-UHFFFAOYSA-N 0.000 claims abstract description 21
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 20
- 229910002804 graphite Inorganic materials 0.000 claims abstract description 20
- 239000010439 graphite Substances 0.000 claims abstract description 20
- 229910052582 BN Inorganic materials 0.000 claims abstract description 19
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 claims abstract description 19
- 239000000843 powder Substances 0.000 claims abstract description 12
- 239000000203 mixture Substances 0.000 claims abstract description 7
- 238000005245 sintering Methods 0.000 claims abstract description 6
- 238000002156 mixing Methods 0.000 claims abstract description 4
- 238000000465 moulding Methods 0.000 claims abstract description 4
- 239000011230 binding agent Substances 0.000 claims description 21
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 11
- 239000002245 particle Substances 0.000 claims description 9
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 8
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 229910052742 iron Inorganic materials 0.000 claims description 5
- 230000001590 oxidative effect Effects 0.000 claims description 5
- 229910000531 Co alloy Inorganic materials 0.000 claims description 4
- 229910052759 nickel Inorganic materials 0.000 claims description 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 3
- 239000010936 titanium Substances 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- 238000000034 method Methods 0.000 abstract description 4
- 230000007797 corrosion Effects 0.000 abstract description 2
- 238000005260 corrosion Methods 0.000 abstract description 2
- 239000012071 phase Substances 0.000 description 34
- 239000000126 substance Substances 0.000 description 20
- 150000002739 metals Chemical class 0.000 description 17
- 239000000314 lubricant Substances 0.000 description 6
- 238000005469 granulation Methods 0.000 description 4
- 230000003179 granulation Effects 0.000 description 4
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 3
- 229910052982 molybdenum disulfide Inorganic materials 0.000 description 3
- 229910001069 Ti alloy Inorganic materials 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000013011 mating Effects 0.000 description 2
- 239000011812 mixed powder Substances 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000009864 tensile test Methods 0.000 description 2
- 229910000851 Alloy steel Inorganic materials 0.000 description 1
- 229910000975 Carbon steel Inorganic materials 0.000 description 1
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical group CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- 229910000990 Ni alloy Inorganic materials 0.000 description 1
- 229910001347 Stellite Inorganic materials 0.000 description 1
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 1
- 229910001634 calcium fluoride Inorganic materials 0.000 description 1
- 239000010962 carbon steel Substances 0.000 description 1
- AHICWQREWHDHHF-UHFFFAOYSA-N chromium;cobalt;iron;manganese;methane;molybdenum;nickel;silicon;tungsten Chemical compound C.[Si].[Cr].[Mn].[Fe].[Co].[Ni].[Mo].[W] AHICWQREWHDHHF-UHFFFAOYSA-N 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910000856 hastalloy Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910001026 inconel Inorganic materials 0.000 description 1
- QLOAVXSYZAJECW-UHFFFAOYSA-N methane;molecular fluorine Chemical compound C.FF QLOAVXSYZAJECW-UHFFFAOYSA-N 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、各種の機械部品として
用いられる軸受材料又はしゅう動材料に適する自己潤滑
性複合材およびその製造方法に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a self-lubricating composite material suitable for bearing materials or sliding materials used as various mechanical parts, and a method for producing the same.
【0002】0002
【従来の技術】従来、二硫化タングステン、二硫化モリ
ブデン、黒鉛、フッ化黒鉛、フッ化カルシウムなどの潤
滑性物質と各種の金属及び合金とからなる焼結体が自己
潤滑性材として使用されている。これら従来の自己潤滑
性材が記載されている代表的なものとしては特開昭53
−122059号公報、特開昭62−196351号公
報などがある。[Prior Art] Conventionally, sintered bodies made of lubricating substances such as tungsten disulfide, molybdenum disulfide, graphite, graphite fluoride, and calcium fluoride, and various metals and alloys have been used as self-lubricating materials. There is. Representative examples of these conventional self-lubricating materials include JP-A-53
-122059, JP-A-62-196351, etc.
【0003】二硫化タングステン、二硫化モリブデン又
は黒鉛などの潤滑性物質と、各種の金属及び合金の結合
相からなる自己潤滑性材は、潤滑性物質としての出発原
料粉末と結合相としての出発原料粉末とを混合、成形後
焼結しているが、こうして得た焼結体の中の潤滑性物質
は結合相の金属及び合金と反応して潤滑性のない物質に
変化して、その歩留りを低下させるか、金属又は合金と
の濡れ性が悪いために結合力が低く、自己潤滑性材の摩
耗の増大及び強度低下をもたらし、寿命が著しく低下し
てしまうという問題がある。さらに、二硫化タングステ
ン、二硫化モリブデン又は黒鉛などの潤滑性物質を含む
自己潤滑性材料は大気中で300℃以上の温度になると
酸化して潤滑性が無くなってしまう。そのため大気中に
て高温で使用することが困難である。A self-lubricating material consisting of a lubricating substance such as tungsten disulfide, molybdenum disulfide or graphite and a binder phase of various metals and alloys is a self-lubricating material consisting of a starting material powder as the lubricating substance and a starting material powder as the binder phase. The lubricating substance in the sintered body thus obtained reacts with the metal and alloy of the binder phase and changes to a non-lubricating substance, reducing the yield. There is a problem in that the bond strength is low due to poor wettability with metals or alloys, resulting in increased wear and decreased strength of self-lubricating materials, resulting in a significant reduction in service life. Furthermore, self-lubricating materials containing lubricating substances such as tungsten disulfide, molybdenum disulfide, or graphite oxidize and lose their lubricity when exposed to temperatures of 300° C. or higher in the atmosphere. Therefore, it is difficult to use it in the atmosphere at high temperatures.
【0004】0004
【発明が解決しようとする課題】本発明は、上述のよう
な問題点を解決したもので、高温および真空中での摩擦
係数及び比摩耗率が低く、しかも機械的性質に優れた自
己潤滑性複合材料及びその製造方法の提供を目的とする
ものである。[Problems to be Solved by the Invention] The present invention solves the above-mentioned problems, and has a self-lubricating property with low friction coefficient and specific wear rate at high temperatures and in vacuum, and excellent mechanical properties. The purpose of this invention is to provide a composite material and a method for manufacturing the same.
【0005】[0005]
【課題を解決するための手段】本発明は、自己潤滑性複
合材料における潤滑性物質と結合相の金属及び合金との
反応性や濡れ性について検討した結果、潤滑性物質の組
成、そのサイズと結合相の金属及び合金との結合性に特
定の元素が効果的に作用するという知見を得ることによ
って発明を完成するに至ったものである。[Means for Solving the Problems] As a result of studying the reactivity and wettability between the lubricating substance and the metal and alloy of the binder phase in self-lubricating composite materials, the present invention has developed the composition of the lubricating substance, its size, and the like. The invention was completed by obtaining the knowledge that specific elements effectively affect the bonding properties of the binder phase with metals and alloys.
【0006】すなわち、本発明は、窒化ホウ素と二硫化
タングステンおよび黒鉛を含む、粒径20μm 以上2
000μm 以下の粒状潤滑性物質相を、5体積%以上
80体積%以下含み、残りが鉄系合金の結合相からなる
ことを特徴とする自己潤滑性複合材である。That is, the present invention provides a particle size of 20 μm or more containing boron nitride, tungsten disulfide, and graphite.
The present invention is a self-lubricating composite material characterized in that it contains 5% by volume or more and 80% by volume or less of a granular lubricating substance phase with a particle diameter of 000 μm or less, and the remainder consists of a binder phase of an iron-based alloy.
【0007】窒化ホウ素は化学的に安定な物質で、大気
中では最も高温まで摩擦係数の低い物質である。しかし
ながら、化学的に安定であることは反面、金属及び合金
との濡れ性、結合性が悪く、これまで窒化ホウ素を用い
た金属及び合金の自己潤滑性複合材はほとんどなく、あ
っても機械的強度が低く、使用に耐えられなかった。ま
た、二硫化タングステンは金属及び合金と反応し易く、
焼結時に潤滑性のない物質に変質し、金属及び合金中の
歩留りが極端に低かった。そこで潤滑性物質と結合相の
金属及び合金との濡れ性、反応性について詳細に検討し
た結果、黒鉛を添加することにより問題点を解決するこ
とができることが分かった。すなわち、窒化ホウ素と二
硫化タングステンおよび黒鉛を含む粒状潤滑性物相と金
属及び合金の粉末とを混合して成形後、焼結する時に、
黒鉛は優先的に金属及び合金に固溶して窒化ホウ素と金
属及び合金とを強固に結合させ、同時に二硫化タングス
テンが金属及び合金と反応して、潤滑性のない物質に変
質するのを阻止することを明らかにした。このようにし
て機械的強度が高く、大気中から真空中までのあらゆる
雰囲気中で、しかも高温においても潤滑性に優れた焼結
体を造ることができる。[0007] Boron nitride is a chemically stable substance and has the lowest coefficient of friction up to the highest temperature in the atmosphere. However, while it is chemically stable, it has poor wettability and bonding properties with metals and alloys, and so far there have been few self-lubricating composites of metals and alloys using boron nitride, and even if there are, it has poor wettability and bonding properties with metals and alloys. It had low strength and could not be used. In addition, tungsten disulfide easily reacts with metals and alloys,
During sintering, it transformed into a substance with no lubricity, and its yield in metals and alloys was extremely low. As a result of a detailed study of the wettability and reactivity between the lubricating substance and the metal or alloy of the binder phase, it was found that the problem could be solved by adding graphite. That is, when a granular lubricating phase containing boron nitride, tungsten disulfide, and graphite is mixed with metal and alloy powder, molded, and then sintered,
Graphite preferentially dissolves in metals and alloys to firmly bond boron nitride with metals and alloys, and at the same time prevents tungsten disulfide from reacting with metals and alloys and changing into a substance with no lubricity. announced that it would. In this way, it is possible to produce a sintered body that has high mechanical strength and excellent lubricity in all atmospheres from air to vacuum, and even at high temperatures.
【0008】[0008]
【作用】本発明の自己潤滑性複合材料は、潤滑性物質を
主成分とする相を金属及び合金の結合相が取り囲んだ構
造によって焼結体の強度が高く、しかも複合材料中に含
まれる潤滑性物質が使用時に相手材との接触面に被膜と
して供給されることによって大気中ないし真空中で高温
まで、比摩耗率と摩擦係数の両者を著しく低下している
ものである。[Function] The self-lubricating composite material of the present invention has a structure in which a phase containing a lubricating substance as a main component is surrounded by a binder phase of metals and alloys, so the strength of the sintered body is high. During use, the material is supplied as a film to the contact surface with the mating material, thereby significantly reducing both the specific wear rate and the coefficient of friction at high temperatures in the air or vacuum.
【0009】すなわち、本発明の自己潤滑性複合材料は
、窒化ホウ素と二硫化タングステンをおよび黒鉛を主成
分とする、粒径20μm 以上2000μm 以下の粒
状潤滑性物質相を、5体積%以上80体積%以下含み、
残りが金属及び合金の結合相からなることを特徴とし、
上記粒状潤滑性物質相は、窒化ホウ素と二硫化タングス
テン及び黒鉛をそれぞれ、少なくとも3体積%以上含み
、さらに結合相は、鉄系合金、ニッケル系合金、コバル
ト系合金及びチタン系合金等の少なくとも1種からなる
ものである。That is, the self-lubricating composite material of the present invention contains a granular lubricating material phase whose main components are boron nitride, tungsten disulfide, and graphite and has a particle size of 20 μm or more and 2000 μm or less, in an amount of 5% by volume or more and 80% by volume. Including % or less,
characterized in that the remainder consists of a binder phase of metals and alloys,
The granular lubricant phase contains boron nitride, tungsten disulfide, and graphite each in an amount of at least 3% by volume, and the binder phase contains at least one of iron-based alloy, nickel-based alloy, cobalt-based alloy, titanium-based alloy, etc. It consists of seeds.
【0010】窒化ホウ素と二硫化タングステン及び黒鉛
を主成分とし、粒径20μm 以上2000μm 以下
の粒状潤滑性物相の占める体積が5%未満であると高温
及び真空中での潤滑性が発揮できず、逆に体積の和が8
0%超になると焼結体の強度が低下して複合材の形成が
困難となる。このため粒状潤滑性物相の占める割合は5
体積%以上80体積%以下とする。窒化ホウ素と二硫化
タングステン及び黒鉛を主成分とする粒状潤滑性物相の
大きさが、20μm 未満であると分散性が悪く、また
結合相と反応し、複合材料の摩擦係数が増大して潤滑性
が低下し、2000μm 超になると結合相の厚みが増
大して摩擦係数が増大する。このため、粒状潤滑性物質
相の大きさは20μm 以上2000μm 以下とする
。粒状潤滑性物相において、窒化ホウ素と二硫化タング
ステン及び黒鉛の占める体積がそれぞれ3%未満である
と、窒化ホウ素の特徴である高温の潤滑性、及び二硫化
タングステンの特徴である真空中での潤滑性が発揮でき
ない。さらに、黒鉛はそれ自身潤滑性があるが、3%未
満であると窒化ホウ素と金属及び合金との結合力を弱め
、同時に二硫化タングステンと金属及び合金との反応を
阻止できなくなる。そのため窒化ホウ素と二硫化グステ
ン及び黒鉛の占める体積を3%以上とすることが望まし
い。[0010] If the volume occupied by the granular lubricating phase, which is mainly composed of boron nitride, tungsten disulfide and graphite and has a particle size of 20 μm or more and 2000 μm or less, is less than 5%, it will not be able to exhibit lubricity at high temperatures and in vacuum. , conversely, the sum of volumes is 8
If it exceeds 0%, the strength of the sintered body decreases, making it difficult to form a composite material. Therefore, the proportion of the granular lubricating phase is 5
% by volume or more and 80% by volume or less. If the size of the granular lubricating phase, which is mainly composed of boron nitride, tungsten disulfide, and graphite, is less than 20 μm, it will have poor dispersibility and will react with the binder phase, increasing the friction coefficient of the composite material and making it difficult to lubricate. If the thickness exceeds 2000 μm, the thickness of the binder phase increases and the coefficient of friction increases. For this reason, the size of the particulate lubricating material phase is set to 20 μm or more and 2000 μm or less. If boron nitride, tungsten disulfide, and graphite each occupy less than 3% of the volume in the granular lubricity phase, boron nitride's characteristic high-temperature lubricity and tungsten disulfide's characteristic lubricity in vacuum are Lubricity cannot be achieved. Furthermore, although graphite itself has lubricating properties, if it is less than 3%, it weakens the bonding force between boron nitride and metals and alloys, and at the same time it becomes impossible to prevent the reaction between tungsten disulfide and metals and alloys. Therefore, it is desirable that the volume occupied by boron nitride, gsten disulfide, and graphite be 3% or more.
【0011】これらの潤滑性物質相を取り囲む結合相は
潤滑性物質相を保持するとともに、焼結時に潤滑性物質
相の変質と消失を抑制し、潤滑性物質と強固な結合を形
成するものである。この結合は潤滑性物質相の組成や使
用環境によって種々の構成にすることができる。耐食性
及び耐熱性を必要とする場合は、炭素鋼、合金鋼ステン
レス鋼などの鉄系合金、インコネル、ハステロイなどの
ニッケル系合金、ステライトなどのコバルト系合金、T
i−6Al−4Vなどのチタン系合金等を結合相にする
ことができる。[0011] The binder phase surrounding these lubricant material phases holds the lubricant material phase, suppresses deterioration and disappearance of the lubricant material phase during sintering, and forms a strong bond with the lubricant material. be. This bond can have various configurations depending on the composition of the lubricating material phase and the environment of use. When corrosion resistance and heat resistance are required, iron-based alloys such as carbon steel, alloy steel and stainless steel, nickel-based alloys such as Inconel and Hastelloy, cobalt-based alloys such as Stellite, and T
A titanium alloy such as i-6Al-4V or the like can be used as the binder phase.
【0012】本発明の自己潤滑性複合材料の製造方法に
おいて、粒状相をつくる造粒工程は一般に行われている
造粒方法が利用できる。例えば、回転ドラム中で、潤滑
性物質を主成分とする混合粉末に、水、アルコール、エ
チルシリケート、水ガラスなどを添加しながら造粒する
方法、あるいは潤滑性物質を主成分とする混合粉末を加
圧成形し、次いで粉砕して造粒する方法などである。造
粒後は非酸化性雰囲気中で500〜1200℃で加熱処
理を行うと、原料粉末に含まれているガスなどを追い出
すことができ、また、造粒粉が硬くなって取扱が容易に
なって好ましい。In the method for producing the self-lubricating composite material of the present invention, a commonly used granulation method can be used for the granulation step to form a granular phase. For example, a mixed powder mainly composed of a lubricating substance is granulated in a rotating drum while adding water, alcohol, ethyl silicate, water glass, etc., or a mixed powder mainly composed of a lubricating substance is granulated. This method includes pressure molding, followed by crushing and granulation. After granulation, heat treatment at 500 to 1200°C in a non-oxidizing atmosphere can drive out gases contained in the raw material powder, and also makes the granulated powder harder and easier to handle. It is preferable.
【0013】本発明の自己潤滑性複合材の製造方法は、
窒化ホウ素と二硫化タングステン及び黒鉛を主成分とし
、粒径20μm 以上2000μm 以下の粒状潤滑性
物質の粉末と、鉄系合金、ニッケル系合金、コバルト系
合金及びチタン系合金等の少なくとも1種からなる結合
相形成用の合金粉末とを、混合及び成形後、非酸化性雰
囲気中で700℃以上1300℃以下の温度で焼結する
ことを特徴とする。温度700℃未満では焼結の進行が
ほとんどなく、1300℃を越えると潤滑性物質が分解
ないし変質してしまうため、焼結温度を700℃以上1
300℃以下とする。酸化性雰囲気中では潤滑性物質が
酸化してしまうため非酸化性雰囲気が望ましい。[0013] The method for producing the self-lubricating composite material of the present invention includes:
The main components are boron nitride, tungsten disulfide, and graphite, and it consists of powder of a granular lubricating substance with a particle size of 20 μm or more and 2000 μm or less, and at least one of iron-based alloys, nickel-based alloys, cobalt-based alloys, titanium-based alloys, etc. The alloy powder for forming a binder phase is mixed and formed, and then sintered at a temperature of 700° C. or higher and 1300° C. or lower in a non-oxidizing atmosphere. If the temperature is less than 700°C, sintering will hardly progress, and if it exceeds 1300°C, the lubricating substance will decompose or change in quality.
The temperature shall be 300℃ or less. A non-oxidizing atmosphere is desirable since the lubricating substance will be oxidized in an oxidizing atmosphere.
【0014】[0014]
【実施例】窒化ホウ素と二硫化タングステン及び黒鉛を
主成分とし、粒径20μm 以上2000μm 以下の
粒状潤滑性物相粉末および結合相の鉄粉末、ステンレス
鋼などの金属及び合金の粉末とをボールミルを用いて混
合した後、プレス成形機で3トン/cm2 の圧力で圧
粉体を作成した。その圧粉体を真空中で焼結した後、引
張試験と摩擦摩耗試験を行った。[Example] A granular lubricating solid phase powder containing boron nitride, tungsten disulfide, and graphite as the main components and having a particle size of 20 μm to 2000 μm, iron powder as a binder phase, and powder of metals and alloys such as stainless steel is milled in a ball mill. After mixing using a press molding machine at a pressure of 3 tons/cm2, a green compact was produced. After sintering the compact in vacuum, a tensile test and a friction and wear test were conducted.
【0015】引張試験には3×2×30mmの試験片を
用いた。摩擦係数は円板状の試料にSUS304を相手
材にして、速度60m/min 、面圧50kg/cm
2 の条件で端面接触して求めたものであり、比摩耗率
は面圧100kg/cm2 、摩擦距離500m の条
件より求めたものである。真空中の摩擦係数は10−5
torrの真空度で測定した。[0015] A test piece of 3 x 2 x 30 mm was used for the tensile test. The coefficient of friction was measured using a disc-shaped sample with SUS304 as the mating material, at a speed of 60 m/min, and a surface pressure of 50 kg/cm.
2, and the specific wear rate was determined under the conditions of a surface pressure of 100 kg/cm2 and a friction distance of 500 m. The coefficient of friction in vacuum is 10-5
It was measured at a vacuum degree of torr.
【0016】本発明の潤滑性物質を主体にした粒状相の
粒度、配合量およびその組成と結合相の組成と製造条件
を表1に示した。焼結体の引張強度と摩擦係数及び比摩
耗率を表2に示した。本発明をはずれた比較例の組成と
、製造条件、焼結体の特性も表1、表2に記載した。Table 1 shows the particle size, blending amount and composition of the granular phase mainly composed of the lubricating substance of the present invention, as well as the composition and manufacturing conditions of the binder phase. Table 2 shows the tensile strength, friction coefficient, and specific wear rate of the sintered body. The compositions, manufacturing conditions, and characteristics of the sintered bodies of comparative examples other than those of the present invention are also listed in Tables 1 and 2.
【0017】本発明品は試料番号1から3であり、結合
相が鉄系合金、ニッケル合金、チタン合金の例である。
本発明の材料は引張強度が20kg/mm2 以上で、
大気及び真空中の摩擦係数は0.2以下で強度、潤滑性
ともに優れた自己潤滑性複合材料である。本発明よりは
ずれた比較例は試料番号4から6に示す。試料番号4は
黒鉛を含まないため、試料番号6は摩擦係数が小さいも
のの焼結体の強度が低い。試料番号5はWS2 を含ま
ないために真空中での摩擦係数が大きい。試料番号6は
潤滑性物質の配合量が少ないために、強度は高いものの
、摩擦係数、比摩耗率ともに大きい。The products of the present invention are sample numbers 1 to 3, and are examples in which the binder phase is an iron alloy, a nickel alloy, or a titanium alloy. The material of the present invention has a tensile strength of 20 kg/mm2 or more,
It is a self-lubricating composite material with a friction coefficient of 0.2 or less in air and vacuum, and excellent in both strength and lubricity. Comparative examples deviating from the present invention are shown in sample numbers 4 to 6. Since sample number 4 does not contain graphite, sample number 6 has a small coefficient of friction but a low strength of the sintered body. Sample No. 5 does not contain WS2 and therefore has a large friction coefficient in vacuum. Sample No. 6 contains a small amount of lubricant, so although its strength is high, its friction coefficient and specific wear rate are both high.
【0018】[0018]
【表1】[Table 1]
【0019】[0019]
【表2】[Table 2]
【0020】[0020]
【発明の効果】本発明の自己潤滑性複合材料は摩擦係数
と比摩耗率が低く、かつ機械的性質に優れたもので、こ
れまで使用できなかった高温ならびに苛酷な雰囲気で使
用することができる画期的な材料である。[Effects of the invention] The self-lubricating composite material of the present invention has a low coefficient of friction and a low specific wear rate, and has excellent mechanical properties, and can be used at high temperatures and harsh environments that were previously unusable. It is a revolutionary material.
Claims (4)
び黒鉛を主成分とする粒径20μm 以上2000μm
以下の粒状潤滑性物相を、5体積%以上80体積%以
下含み、残りが金属及び合金の結合相からなることを特
徴とする自己潤滑性複合材料。[Claim 1] Particles containing boron nitride, tungsten disulfide, and graphite as main components with a diameter of 20 μm or more and 2000 μm
A self-lubricating composite material comprising 5% by volume or more and 80% by volume or less of the following particulate lubricating material phase, with the remainder consisting of a binder phase of metal and alloy.
化タングステン及び黒鉛を、それぞれ、少なくとも3体
積%含んでいる請求項1記載の自己潤滑性複合材料。2. The self-lubricating composite material of claim 1, wherein the particulate lubricating phase contains at least 3% by volume of each of boron nitride, tungsten disulfide, and graphite.
、コバルト系合金及びチタン系合金の少なくとも1種か
らなる請求項1または2記載の自己潤滑性複合材。3. The self-lubricating composite material according to claim 1, wherein the binder phase comprises at least one of an iron-based alloy, a nickel-based alloy, a cobalt-based alloy, and a titanium-based alloy.
成分とする粒径20μm 以上2000μm 以下の粒
状粉末と、結合相形成用の合金粉末とを、混合及び成形
後、非酸化性雰囲気中で700℃以上1300℃以下の
温度で焼結することを特徴とする自己潤滑性複合材料の
製造方法。4. After mixing and molding granular powder containing boron nitride and tungsten disulfide and having a particle size of 20 μm or more and 2000 μm or less and an alloy powder for forming a binder phase, the mixture is heated at 700° C. in a non-oxidizing atmosphere. A method for producing a self-lubricating composite material, characterized in that sintering is performed at a temperature of 1300°C or less.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8692291A JPH04320497A (en) | 1991-04-18 | 1991-04-18 | Self-lubricating composite material and its preparation |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8692291A JPH04320497A (en) | 1991-04-18 | 1991-04-18 | Self-lubricating composite material and its preparation |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04320497A true JPH04320497A (en) | 1992-11-11 |
Family
ID=13900351
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP8692291A Withdrawn JPH04320497A (en) | 1991-04-18 | 1991-04-18 | Self-lubricating composite material and its preparation |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04320497A (en) |
-
1991
- 1991-04-18 JP JP8692291A patent/JPH04320497A/en not_active Withdrawn
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