JP3003889B2 - Sliding material - Google Patents
Sliding materialInfo
- Publication number
- JP3003889B2 JP3003889B2 JP4-47544A JP4754492A JP3003889B2 JP 3003889 B2 JP3003889 B2 JP 3003889B2 JP 4754492 A JP4754492 A JP 4754492A JP 3003889 B2 JP3003889 B2 JP 3003889B2
- Authority
- JP
- Japan
- Prior art keywords
- sintered
- sintered layer
- layer
- sliding
- solid lubricant
- 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 - Lifetime
Links
- 239000000463 material Substances 0.000 title claims description 36
- 239000002245 particle Substances 0.000 claims description 33
- 239000007787 solid Substances 0.000 claims description 32
- 239000000314 lubricant Substances 0.000 claims description 29
- 229910052751 metal Inorganic materials 0.000 claims description 28
- 239000002184 metal Substances 0.000 claims description 28
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 25
- 229910002804 graphite Inorganic materials 0.000 claims description 25
- 239000010439 graphite Substances 0.000 claims description 25
- 238000005461 lubrication Methods 0.000 claims description 19
- CWQXQMHSOZUFJS-UHFFFAOYSA-N Molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 claims description 18
- 229910052982 molybdenum disulfide Inorganic materials 0.000 claims description 18
- 239000002923 metal particle Substances 0.000 claims description 8
- 229910000881 Cu alloy Inorganic materials 0.000 claims description 7
- 229920003002 synthetic resin Polymers 0.000 claims description 5
- 239000000057 synthetic resin Substances 0.000 claims description 5
- ITRNXVSDJBHYNJ-UHFFFAOYSA-N Tungsten(IV) sulfide Chemical compound S=[W]=S ITRNXVSDJBHYNJ-UHFFFAOYSA-N 0.000 claims description 2
- 239000010410 layer Substances 0.000 description 74
- 239000000843 powder Substances 0.000 description 28
- 239000011347 resin Substances 0.000 description 23
- 229920005989 resin Polymers 0.000 description 23
- 239000010949 copper Substances 0.000 description 13
- 238000005245 sintering Methods 0.000 description 13
- 229910052802 copper Inorganic materials 0.000 description 11
- 229910000906 Bronze Inorganic materials 0.000 description 10
- 238000005299 abrasion Methods 0.000 description 10
- 239000010974 bronze Substances 0.000 description 10
- 238000005520 cutting process Methods 0.000 description 10
- 238000001035 drying Methods 0.000 description 9
- 239000004962 Polyamide-imide Substances 0.000 description 8
- 229920002312 polyamide-imide Polymers 0.000 description 8
- 230000001788 irregular Effects 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 229910015800 MoS Inorganic materials 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000011148 porous material Substances 0.000 description 5
- 230000023298 conjugation with cellular fusion Effects 0.000 description 4
- 238000005470 impregnation Methods 0.000 description 4
- 230000013011 mating Effects 0.000 description 4
- 230000021037 unidirectional conjugation Effects 0.000 description 4
- 239000005662 Paraffin oil Substances 0.000 description 3
- 229920001721 Polyimide Polymers 0.000 description 3
- 239000004642 Polyimide Substances 0.000 description 3
- 229910045601 alloy Inorganic materials 0.000 description 3
- 239000000956 alloy Substances 0.000 description 3
- REDXJYDRNCIFBQ-UHFFFAOYSA-N aluminium(3+) Chemical class [Al+3] REDXJYDRNCIFBQ-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000005011 phenolic resin Substances 0.000 description 3
- 239000011342 resin composition Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive Effects 0.000 description 2
- 229910021383 artificial graphite Inorganic materials 0.000 description 2
- 238000003754 machining Methods 0.000 description 2
- 238000001000 micrograph Methods 0.000 description 2
- 239000003595 mist Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- 102200129688 ETFDH F16C Human genes 0.000 description 1
- 102200082816 HBB S45C Human genes 0.000 description 1
- ZQKXQUJXLSSJCH-UHFFFAOYSA-N Melamine cyanurate Chemical compound NC1=NC(N)=NC(N)=N1.O=C1NC(=O)NC(=O)N1 ZQKXQUJXLSSJCH-UHFFFAOYSA-N 0.000 description 1
- 239000004697 Polyetherimide Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 150000002019 disulfides Chemical class 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 229910052745 lead Inorganic materials 0.000 description 1
- 230000001050 lubricating Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000011812 mixed powder Substances 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 239000002365 multiple layer Substances 0.000 description 1
- 229910021382 natural graphite Inorganic materials 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229920005587 polyester-imide Polymers 0.000 description 1
- 229920001601 polyetherimide Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching Effects 0.000 description 1
- 238000005057 refrigeration Methods 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 230000002522 swelling Effects 0.000 description 1
- 230000002195 synergetic Effects 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
Description
【0001】[0001]
【産業上の利用分野】本発明は、混合潤滑や境界潤滑条
件ですぐれた摺動特性を有する摺動材料に関するもので
あり、さらに詳しく述べるならば、裏金と、この裏金表
面に焼結されたCuまたはCu合金焼結層と、この焼結
層の焼結粒子の空間に充填された合成樹脂及び固体潤滑
剤とを含んでなる摺動材料に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a sliding material having excellent sliding characteristics under mixed lubrication and boundary lubrication conditions. More specifically, the present invention relates to a backing metal and a sintered body formed on the surface of the backing metal. The present invention relates to a sliding material including a Cu or Cu alloy sintered layer, and a synthetic resin and a solid lubricant filled in spaces of sintered particles of the sintered layer.
【0002】[0002]
【従来の技術】特開昭55−106230号公報によれ
ば、多孔率88〜98%のCuなどの海綿状金属の空隙
部にポリイミドと、30重量%以下の二硫化モリブデ
ン、グラファイトなどの添加剤とを充填した摺動部材が
公知である。この摺動部材は多孔率が非常に大きい海綿
状金属を充填物質の保持基材として使用したものであ
る。したがって、通常焼結で作られる海綿状金属を所定
の軸受形状に加工するには同公報の実施例に示されてい
るように打ち抜き加工をすることが通常必要になり、歩
留まり低下の問題に加えて裏金を使用した摺動材料より
は加工性が劣る問題がある。According to JP-A-55-106230, polyimide and 30% by weight or less of molybdenum disulfide, graphite and the like are added to voids of spongy metal such as Cu having a porosity of 88 to 98%. A sliding member filled with an agent is known. This sliding member uses a spongy metal having a very high porosity as a base material for holding a filling substance. Therefore, in order to form a spongy metal, which is usually produced by sintering, into a predetermined bearing shape, it is usually necessary to perform a punching process as shown in the embodiment of the publication, and in addition to the problem of reduced yield, Therefore, there is a problem that the workability is inferior to that of the sliding material using the back metal.
【0003】特公昭63−37445号公報によれば、
裏金と、この裏金表面に焼結されたCuまたはCu合金
焼結層と、この焼結層の焼結粒子の空間に充填された合
成樹脂及び固体潤滑剤とを含んでなり、前記焼結層及び
充填物質の表面を機械加工して実質的に同一平面にして
なる摺動材料が開示されている。According to JP-B-63-37445,
A back metal, a Cu or Cu alloy sintered layer sintered on the surface of the back metal, and a synthetic resin and a solid lubricant filled in the space of the sintered particles of the sintered layer; And a sliding material in which the surface of the filling material is machined to be substantially coplanar.
【0004】[0004]
【発明が解決しようとする課題】前掲特公昭63−37
445号の摺動材料を製造する製造法の説明によると、
略球形の直径が0.18mmの鉛青銅粉末を裏金に焼結
し、これを0.11mmの厚みになるように機械加工す
ることによって焼結金属の表面露出率が40〜60%の
摺動材料表面を得ている。焼結層が1層の金属粒子から
構成されていると、機械加工による削り代により表面露
出率が大きく変動し、摺動特性が安定しない。また、金
属粒子を2層以上に積み重ねた焼結層を作成し、これを
機械加工すると、金属粒子が最密充填に積み重ねている
ならば、表面露出率は削り代に関係なく一定になるはず
であるが、実際は図4に示すように切削量(削り代)に
依存する。[Problems to be Solved by the Invention]
According to the description of the manufacturing method for manufacturing the sliding material of No. 445,
A lead-bronze powder having a substantially spherical diameter of 0.18 mm is sintered on a backing metal and machined so as to have a thickness of 0.11 mm. The material surface is getting. If the sintered layer is composed of one layer of metal particles, the surface exposure rate fluctuates greatly due to the machining allowance, and the sliding characteristics are not stable. Also, if a sintered layer is created by stacking two or more metal particles and then machined, if the metal particles are stacked in close packing, the surface exposure rate should be constant regardless of the cutting allowance. However, it actually depends on the cutting amount (cutting allowance) as shown in FIG.
【0005】図4は、平均粒径が110μmの球状粉末
を略3層(部分的には2または4層になるとこともあ
る)に積み重ねて焼結し、約300μmの厚みおよび約
35体積%の空孔率の焼結層を形成し、樹脂を焼結層の
表面から更に約20μm突出するように焼結層全体に含
浸させて摺動層を作り、これを機械加工により切削した
時の切削量(μm)と焼結層の表面露出率の関係を求め
たグラフである。このグラフより表面露出率を安定させ
るには多層に積み重ねられた焼結粒子を100μm以上
切削しなければならないことが分かる。FIG. 4 shows that spherical powder having an average particle size of 110 μm is stacked and sintered in approximately three layers (partially two or four layers), and has a thickness of about 300 μm and a volume of about 35% by volume. A sintering layer having a porosity of is formed, and a resin is impregnated into the entire sintering layer so as to protrude further from the surface of the sintering layer by about 20 μm to form a sliding layer, which is cut by machining. It is the graph which calculated | required the relationship between the cutting amount (micrometer) and the surface exposure rate of a sintered layer. From this graph, it can be seen that in order to stabilize the surface exposure rate, the sintered particles stacked in multiple layers must be cut by 100 μm or more.
【0006】前掲特公昭の摺動材料においては二硫化モ
リブデン、グラファイトなどの固体潤滑剤は30重量%
以下が望ましいと説明されている。固体潤滑剤の量が3
0重量%以下では結合力が強いポリイミド、ポリアミド
イミドなどの成分の量が多いために固体潤滑剤による効
果は十分に発揮されない。また、焼結金属の表面露出率
が大きいと相手材と直接接触する金属の割合が大きくな
り、耐摩耗性は高められ一方で耐焼付性が低下するの
で、このことを勘案して摺動材料の用途により表面露出
率を定めるところであるが、平均表面露出率が例えば2
0%程度と低い場合焼結層が1層の金属粒子から構成さ
れていると、削り代による表面露出率の変動が極めて多
くなり、安定した摺動特性が得られない。すなわち、製
造ロットにより摺動特性が大きく変動するのみならず、
摺動中にも樹脂が少し摩耗すると急激に焼結金属の表面
露出割合が増大するので、摺動特性が大きく変動する。
このような状況では相手材と摺動材料とのなじみが取れ
ていないことが多いので、両者間の金属接触によりいず
れかの材料が急激に摩耗し、焼付に至り、非常に好まし
くない。本発明は上記した欠点を解消した摺動材料を提
供することを目的とする。[0006] In the sliding material of the above-mentioned Japanese Patent Publication No. Sho-sho, solid lubricants such as molybdenum disulfide and graphite are 30% by weight.
The following is described as being desirable. The amount of solid lubricant is 3
When the content is 0% by weight or less, the effect of the solid lubricant is not sufficiently exhibited because the amount of components such as polyimide and polyamide imide having a strong bonding force is large. In addition, if the surface exposure ratio of the sintered metal is large, the proportion of the metal that comes into direct contact with the mating material increases, and the wear resistance is increased while the seizure resistance is reduced. The surface exposure rate is to be determined depending on the application of
When the sintered layer is composed of a single layer of metal particles, the fluctuation of the surface exposure rate due to the shaving margin becomes extremely large, and stable sliding characteristics cannot be obtained. That is, not only the sliding characteristics fluctuate greatly depending on the production lot,
If the resin wears a little during sliding, the surface exposure ratio of the sintered metal sharply increases, so that the sliding characteristics fluctuate greatly.
In such a situation, the mating material and the sliding material are often unfamiliar with each other, so that one of the materials rapidly wears out due to metal contact between the two, resulting in seizure, which is extremely undesirable. An object of the present invention is to provide a sliding material which has solved the above-mentioned disadvantages.
【0007】[0007]
【課題を解決するための手段】本発明に係る摺動材料
は、裏金と、この裏金表面に焼結されたCuまたはCu
合金焼結層と、この焼結層の焼結粒子間の空間に充填さ
れた合成樹脂及び固体潤滑剤とを含んでなり、前記焼結
層及び充填物質の表面を機械加工してなる摺動材料にお
いて、前記焼結層は、2層以上に積層された粒径が30
〜200μmの金属粒子を5〜70体積%の空孔率で焼
結した焼結金属からなり、かつ前記機械加工された表面
における焼結層の表面露出率が95%以下であり、前記
固体潤滑剤は合計量で30〜80重量%の二硫化モリブ
デンとグラファイトからなることを特徴とする。SUMMARY OF THE INVENTION A sliding material according to the present invention comprises a back metal and Cu or Cu sintered on the surface of the back metal.
A sliding comprising an alloy sintered layer and a synthetic resin and a solid lubricant filled in the space between the sintered particles of the sintered layer, wherein the surfaces of the sintered layer and the filling material are machined. In the material, the sintered layer has a particle size of 30 or more laminated in two or more layers.
A metal particle having a porosity of 5 to 70% by volume and a metal layer having a porosity of 5 to 70% by volume, and a surface exposure ratio of a sintered layer on the machined surface is 95% or less; The agent consists of a total of 30 to 80% by weight of molybdenum disulfide and graphite.
【0008】以下本発明の構成を説明する。裏金は特に
種類に制限がなく、公知のものであってよい。Cuまた
はCu合金焼結層は、純銅、あるいは青銅、鉛青銅、リ
ン青銅などののCu合金、あるいはこれら純銅または銅
合金にFeP,Al2 O3 などの粉末を分散した複合材
料を焼結したものである。Hereinafter, the configuration of the present invention will be described. The back metal is not particularly limited in type, and may be a known one. The Cu or Cu alloy sintered layer is formed by sintering pure copper, or a Cu alloy such as bronze, lead bronze, phosphor bronze, or a composite material in which powder such as FeP or Al 2 O 3 is dispersed in these pure copper or copper alloy. Things.
【0009】これらの銅系粉末の形状は球状もしくは鋭
いエッジがない略球状、その他の異形(片状、樹枝状、
鎖状、不等辺多面体等)などである。異形粉を混合した
粉末では、全粒子に含まれる短径/長径比が0.2〜
0.7のものが50%以上、好ましくは70%以上であ
ることが好ましい。短径/長径比が0.7以上の異形粉
が多いと異形粉の効果が発揮されず、一方短径/長径比
が0.2以下の異形粉が多いと所望の平均充填密度が得
られず、やはり異形粉の効果が発揮されない。特に、短
径/長径比が0.2以下の異形粉が全粒子中の30%以
下、好ましくは10%以下であると、異形粉が空孔を密
に充填する傾向を抑えることができる。The shape of these copper-based powders is spherical or substantially spherical without sharp edges, and other irregular shapes (flaky, dendritic,
Chain, inequilateral polyhedron, etc.). In the powder mixed with irregularly shaped powder, the ratio of minor axis / major axis contained in all particles is 0.2 to
It is preferred that 0.7 is 50% or more, preferably 70% or more. When the ratio of minor diameter / major axis is more than 0.7, the effect of irregular shape powder is not exhibited. On the other hand, when the ratio of minor diameter / major axis is less than 0.2, desired average packing density is obtained. However, the effect of irregular shaped powder is not exhibited. In particular, when the irregular powder having a ratio of minor axis / major axis of 0.2 or less is 30% or less, preferably 10% or less of all the particles, the tendency of the irregular powder to densely fill the pores can be suppressed.
【0010】焼結層の特長の一つである焼結粉末の大き
さは平均粒径で30〜200μmであることが必要であ
り、好ましくは50〜200μm、より好ましくは60
〜150μmである。異形粉の場合は長計の平均が30
〜200μmであることが必要である。焼結粉末の大き
さが30μmより小さいと、焼結体の密度が大である
と、空孔に樹脂や固体潤滑剤を含浸することが困難にな
り、また焼結体の密度が小さい場合はCu(合金)粒子
どうしの接着強度が低くなり好ましくない。焼結層の他
の特長である空孔率(体積%)、すなわち樹脂などを含
浸する前の焼結体の気孔の割合は5〜70%であること
が必要であり、好ましくは10〜60%、より好ましく
は30〜50%である。空孔率が5%より小さいと樹脂
と固体潤滑剤の含浸量が低下して、低摩擦性、潤滑性等
の摺動特性が劣化し、焼付が起こりやすくなり、一方7
0%を超えると焼結体の占める割合が少なくなり、強度
が低下して好ましくない。The size of the sintered powder, which is one of the features of the sintered layer, needs to be 30 to 200 μm in average particle diameter, preferably 50 to 200 μm, more preferably 60 to 200 μm.
150150 μm. In the case of irregular shaped powder, the average of the total length is 30
It is necessary to be ~ 200 μm. If the size of the sintered powder is smaller than 30 μm, if the density of the sintered body is large, it becomes difficult to impregnate the pores with a resin or a solid lubricant, and if the density of the sintered body is small, It is not preferable because the adhesive strength between Cu (alloy) particles is lowered. The porosity (volume%), which is another feature of the sintered layer, that is, the proportion of pores in the sintered body before impregnation with a resin or the like must be 5 to 70%, preferably 10 to 60%. %, More preferably 30 to 50%. If the porosity is less than 5%, the impregnation amount of the resin and the solid lubricant decreases, and the sliding characteristics such as low friction and lubricity deteriorate, and seizure easily occurs.
If it exceeds 0%, the proportion occupied by the sintered body decreases, and the strength decreases, which is not preferable.
【0011】焼結層の他の特長である表面における焼結
金属の割合、すなわち焼結層の露出率(面積%)は95
%以下であることが必要であり、85%以下が好まし
く、30〜80%がより好ましい。また用途によって、
一般条件の場合は高い露出率(60〜80%)、潤滑条
件が厳しく耐焼付性を重視する場合は低い露出率(40
〜60%)が望ましい。この焼結層露出率は相手材と向
かい合う部分での摺動材料の特性に大きい影響を与え
る。従来の摺動材料でも焼結層露出率はこのような影響
因子ではあったが、実際には摺動材料の製造方法により
かつ使用中に大きく変動していたために、それを制御す
ることによって摺動特性を意図するものとすることは出
来なかった。しかしながら本発明によれば焼結粒子を2
層以上に積層することにより焼結層露出率の大きな変動
を防ぐことができるので、これを制御して摺動特性向上
することができる。しかして露出率が95%を超えると
固体潤滑剤の効果が少なくなるので、95%以下とする
必要がある。The ratio of the sintered metal on the surface, which is another characteristic of the sintered layer, that is, the exposure rate (area%) of the sintered layer is 95%.
% Or less, preferably 85% or less, more preferably 30 to 80%. Also, depending on the application,
A high exposure rate (60 to 80%) is applied under general conditions, and a low exposure rate (40
~ 60%) is desirable. The sintering layer exposure rate has a large effect on the characteristics of the sliding material at the portion facing the mating material. Although the exposure ratio of the sintered layer was such an influential factor even in the conventional sliding material, in actuality, it varied greatly depending on the manufacturing method of the sliding material and during use. Dynamic characteristics could not be intended. However, according to the present invention, two sintered particles are used.
By laminating more than two layers, it is possible to prevent a large change in the exposure ratio of the sintered layer, and it is possible to control this to improve the sliding characteristics. If the exposure rate exceeds 95%, the effect of the solid lubricant is reduced, so it is necessary to set the exposure rate to 95% or less.
【0012】空孔率は、粉末の粒径が小さいほうが焼結
が進みやすいので小さくなる。ただし、粉末の粒径が大
径と小径の粒子が混合した混合粉を使用することによ
り、同一粒径の粉末と平均粒径が同じであっても、空孔
率は小さくなる。なお本発明で言う空孔率とは焼結層全
体の平均空孔率を指している(局部的な空孔率は図4か
らも窺えるように焼結体表面の方が大きくなってい
る)。The porosity is smaller when the powder particle size is smaller, because sintering proceeds more easily. However, by using a mixed powder in which particles having a large particle diameter and a particle having a small particle diameter are mixed, the porosity is reduced even if the powder having the same particle diameter has the same average particle diameter. The porosity referred to in the present invention refers to the average porosity of the entire sintered layer (the local porosity is larger on the surface of the sintered body as can be seen from FIG. 4). .
【0013】焼結層露出率は、焼結体の空孔率及び削り
代により決定される(図4参照)。焼結層の他の特徴で
ある2層以上の積層構造は、図4に示したように安定し
た焼結層露出率を得るためには、焼結層をある程度深く
表面から削る必要があり、1層構造であると焼結中に粒
子が全体として脱落することもあって、所望の切削量を
得ることができにくいので、2層以上の積層構造に限定
したのである。The sintering layer exposure rate is determined by the porosity and the cutting allowance of the sintered body (see FIG. 4). The laminated structure of two or more layers, which is another feature of the sintered layer, requires that the sintered layer be cut from the surface to some extent in order to obtain a stable sintered layer exposure rate as shown in FIG. If it has a one-layer structure, the particles may fall off as a whole during sintering, and it is difficult to obtain a desired amount of cutting. Therefore, the laminated structure is limited to two or more layers.
【0014】図4に示される球状粉から構成される焼結
層(図5)と異形粉から構成される焼結層(図6)の表
面露出率は前者のほうが後者よりほぼ全切削量領域で1
5〜20%高くなっている。また粉末の充填密度は前者
が4.4〜4.8g/cc(焼結層体積)であり、後者
が3.2〜3.7g/ccであり、したがって後者(前
者)の低(高)充填密度が低(高)露出率に対応してい
る。この結果、異形粉では表面露出率は切削量50〜1
50μmで約30〜60%となり、図1に示される耐焼
付性が高い範囲となる。図6の異形粉の特性は以下のと
おりである。 平均粒径:90μm 短径/長径比:0.2未満−4%(全体の粒子に含まれ
る比率) 短径/長径比:0.2〜0.7−76%(全体の粒子に
含まれる比率) 短径/長径比:0.7超−20%(全体の粒子に含まれ
る比率) 図6の焼結層では粉末の平均充填密度が3.5g/cc
である。The surface exposure ratio of the sintered layer composed of spherical powder (FIG. 5) and the sintered layer composed of irregularly shaped powder (FIG. 6) shown in FIG. 4 is almost the same as that of the latter. At 1
5-20% higher. The packing density of the powder is 4.4 to 4.8 g / cc (sintered layer volume) for the former, and 3.2 to 3.7 g / cc for the latter, and thus the low (high) of the latter (the former) is obtained. The packing density corresponds to a low (high) exposure rate. As a result, in the case of the irregular shaped powder, the surface exposure rate was 50 to 1
It becomes about 30 to 60% at 50 μm, which is the range where the seizure resistance shown in FIG. 1 is high. The characteristics of the irregularly shaped powder of FIG. 6 are as follows. Average particle size: 90 μm Minor axis / major axis ratio: less than 0.2-4% (ratio included in all particles) Minor axis / major axis ratio: 0.2-0.7-76% (included in all particles) Ratio) minor axis / major axis ratio: more than 0.7-20% (ratio included in the whole particles) In the sintered layer of FIG. 6, the average packing density of the powder is 3.5 g / cc.
It is.
【0015】固体潤滑剤は30〜80重量%、好ましく
は35〜55重量%の二硫化モリブデンおよびグラファ
イトを含む必要がある。二硫化モリブデンは耐焼付性を
向上させ、またグラファイトは耐摩耗性を向上させる。
固体潤滑剤の量が35重量%未満であると、混合潤滑あ
るいは境界潤滑条件で焼付や摩耗が起こりやすくなり、
一方80重量%を超えると二硫化モリブデンなどが脱落
しやすくなる。二硫化モリブデンは、摺動層中の含有量
が10〜50重量%、より好ましくは15〜35重量
%、平均粒径が0.5〜25μmの条件で使用すること
が好ましい。グラファイトは摺動層中の含有量が2〜4
0重量%、より好ましくは15〜30重量%、平均粒径
が8〜35μmの条件で使用することが好ましい。グラ
ファイトは天然、人造グラファイトのいずれでもよい
が、等方性人造グラファイトが耐摩耗性の観点から好ま
しい。The solid lubricant must contain 30 to 80% by weight, preferably 35 to 55% by weight of molybdenum disulfide and graphite. Molybdenum disulfide improves seizure resistance, and graphite improves abrasion resistance.
If the amount of the solid lubricant is less than 35% by weight, seizure or wear is likely to occur under mixed lubrication or boundary lubrication conditions,
On the other hand, when it exceeds 80% by weight, molybdenum disulfide and the like are apt to fall off. Molybdenum disulfide is preferably used under the conditions that the content in the sliding layer is 10 to 50% by weight, more preferably 15 to 35% by weight, and the average particle size is 0.5 to 25 μm. The content of graphite in the sliding layer is 2-4.
It is preferably used under the conditions of 0% by weight, more preferably 15 to 30% by weight, and an average particle size of 8 to 35 μm. The graphite may be either natural or artificial graphite, but isotropic artificial graphite is preferred from the viewpoint of abrasion resistance.
【0016】樹脂としては、芳香族ポリイミドとその変
性樹脂であるポリアミドイミド、ポリエーテルイミド、
ポリエステルイミド及びフェノール樹脂などを全部もし
くは主成分として使用する。樹脂の量は固体潤滑剤の残
部であるが、20〜70重量%の範囲内にあることが好
ましい。As the resin, aromatic polyimide and its modified resin, polyamideimide, polyetherimide,
Polyester imide and phenol resin are used in whole or as a main component. The amount of the resin is the balance of the solid lubricant, but is preferably in the range of 20 to 70% by weight.
【0017】上記以外の固体潤滑剤として、二硫化タン
グステン(WS2),BN,PTFE,ふっ素樹脂、P
bなどを3〜20重量%未満、好ましくは5〜20重量
%さらに添加することができる。これらの固体潤滑剤を
使用する時は、二硫化モリブデンとグラファイトの量を
減少させて樹脂の量を最低で20重量%以上に似するこ
とが必要である。As other solid lubricants, tungsten disulfide (WS 2 ), BN, PTFE, fluororesin, P
b and the like can be further added in an amount of 3 to less than 20% by weight, preferably 5 to 20% by weight. When using these solid lubricants, it is necessary to reduce the amount of molybdenum disulfide and graphite to make the amount of resin at least as high as 20% by weight or more.
【0018】続いて上記した摺動材料の製造方法の一例
を説明する。粒径−100メッシュ〜+200メッシュ
の鉛青銅等の粉末を鋼板裏金上に厚みが約300μm
(この場合の積層数は3層)の層状に散布し、800〜
850℃で焼結する。この結果空孔率が約40〜50%
の焼結層が得られる。続いて焼結層が接着された裏金を
固体潤滑剤と樹脂を分散した液中に浸漬する。この際、
乾燥時に膨張して樹脂層の膨れやクラックをもたらすお
それがある焼結層の空気を樹脂で十分に置換することが
重要である。次に、液をミキサで撹拌して固体を焼結空
孔中に含浸する。他の含浸法としては、固体潤滑剤と樹
脂を混合した液を焼結層に塗布して、含浸する方法もあ
る。含浸後例えば150℃で30分間乾燥を行う。乾燥
により溶剤は蒸発するが、焼結層における空気の樹脂に
よる置換を容易にするために溶剤を多く使用して、樹脂
の粘度を低下すると、乾燥による溶剤の蒸発が妨げれら
れ、乾燥時間が長くなる。この点に関してフェノール樹
脂は固形分が例えば60%と多くとも、粘度が低い(例
えば2p)ので、空気の置換を十分に行いかつ乾燥時間
を短くすることができる。乾燥時間はポリアミドイミド
の場合の1/6以下とすることができる。この結果フェ
ノール樹脂を使用すると乾燥のラインスピードを高め
て、膨れやクラックのない製品をつくることができる。Next, an example of a method for manufacturing the above-mentioned sliding material will be described. Powder of lead bronze etc. with a particle size of -100 mesh to +200 mesh is coated on a steel plate backing to a thickness of about 300 μm.
(The number of laminations in this case is 3 layers)
Sinter at 850 ° C. This results in a porosity of about 40-50%
Is obtained. Subsequently, the back metal to which the sintered layer is bonded is immersed in a liquid in which a solid lubricant and a resin are dispersed. On this occasion,
It is important that the air in the sintered layer, which may expand during drying and cause swelling or cracking of the resin layer, be sufficiently replaced with resin. Next, the liquid is stirred with a mixer to impregnate the solid into the sintered pores. As another impregnation method, there is a method in which a liquid in which a solid lubricant and a resin are mixed is applied to a sintered layer to be impregnated. After the impregnation, drying is performed, for example, at 150 ° C. for 30 minutes. The solvent evaporates by drying, but if the viscosity of the resin is reduced by using a large amount of the solvent to facilitate the replacement of the air in the sintered layer by the resin, the evaporation of the solvent due to the drying is hindered, and the drying time is reduced. become longer. In this respect, the phenolic resin has a low viscosity (for example, 2p) even if the solid content is as high as, for example, 60%, so that the air can be sufficiently replaced and the drying time can be shortened. The drying time can be 1/6 or less of the case of polyamide imide. As a result, when a phenol resin is used, the drying line speed can be increased, and a product free of blisters and cracks can be produced.
【0019】乾燥に続いて、例えば300℃で30分間
焼成を行う。続いて最表面から約100μm切削して焼
結層露出率が約70%の摺動層を作成する。また、空孔
率が50%以上の焼結体を得るためには、鉛青銅粉末と
グラファイト粉末の混合分を裏金に散布し、水素気流中
で800〜850℃で焼結を行い、鉛青銅焼結合金層中
に、焼結されないで残留しているグラファイト粉末を集
塵機で吸引することができる。なお、グラファイト粉末
を固体潤滑剤として使用することもでき、この場合は吸
引を行わない。その他に、空孔率が50%以上の焼結体
を得るためにはメラミンシアヌレートなどの300〜5
00℃で昇華する物質を鉛青銅と混合して使用すること
もできる。以上鉛青銅の例について説明したが、その他
の焼結金属についても同様に焼結することができる。Subsequent to drying, baking is performed, for example, at 300 ° C. for 30 minutes. Then, a sliding layer having a sintered layer exposure rate of about 70% is formed by cutting about 100 μm from the outermost surface. Further, in order to obtain a sintered body having a porosity of 50% or more, a mixture of a lead bronze powder and a graphite powder is sprayed on a backing metal, and sintered at 800 to 850 ° C. in a hydrogen stream to obtain a lead bronze. The graphite powder remaining without being sintered in the sintered alloy layer can be sucked by a dust collector. In addition, graphite powder can be used as a solid lubricant, and in this case, suction is not performed. In addition, in order to obtain a sintered body having a porosity of 50% or more, 300 to 5 particles such as melamine cyanurate are required.
A substance that sublimates at 00 ° C. can be used in combination with lead bronze. Although the example of lead bronze has been described above, other sintered metals can be similarly sintered.
【0020】[0020]
【作用】80%Cu,10%Sn,10%Pbの組成の
鉛青銅球状粉、ポリアミドイミド(日立化成社製品HI
−500又はHPC−6000−26)、グラファイト
(東海カーボン社製品G152又はTGP−15)、M
oS2(住鉱潤滑材社製品PAパウダー)を使用して、
上記した製法で各種摺動材料を製造し、平板状試験片を
作成し、円筒軸上回転軸(S45C焼入)を相手材とし
てこれに線接触させ、試験片のその特性を比較評価し
た。なお、切削量は100μmであり、焼結層露出率は
75面積%であった。The lead bronze spherical powder having a composition of 80% Cu, 10% Sn, and 10% Pb, polyamide imide (HI, manufactured by Hitachi Chemical Co., Ltd.)
-500 or HPC-6000-26), graphite (G152 or TGP-15, manufactured by Tokai Carbon Co., Ltd.), M
Using oS 2 (PA powder manufactured by Sumiko Lubricant Co., Ltd.)
Various sliding materials were manufactured by the above-mentioned manufacturing method, and a plate-like test piece was prepared, and was brought into linear contact with a rotating shaft on a cylindrical shaft (S45C quenching) as a mating material, and the characteristics of the test piece were comparatively evaluated. The amount of cutting was 100 μm, and the exposure rate of the sintered layer was 75 area%.
【0021】試験条件は下記の通りであった。 耐摩耗性試験 荷重:10kg 速度:2m/sec 潤滑:5cc/min給油 油種:パラフィン油 すべり距離:1.44×104 m 耐焼付性試験 荷重:10kg 速度:4m/sec 潤滑:0.1cc/minで5分間給油後、オイルカッ
ト 油種:パラフィン油 なお、参考のために前掲特公昭63−37445号にお
ける試験条件を引用して下記に示す。 荷重:250g 速度:0.052m/sec 潤滑:グリースThe test conditions were as follows. Abrasion resistance test Load: 10 kg Speed: 2 m / sec Lubrication: 5 cc / min Lubrication Oil type: paraffin oil Sliding distance: 1.44 × 10 4 m Seizure resistance test Load: 10 kg Speed: 4 m / sec Lubrication: 0.1 cc After oiling at / min for 5 minutes, oil cut Oil type: paraffin oil The test conditions in the above-mentioned JP-B-63-37445 are quoted below for reference. Load: 250g Speed: 0.052m / sec Lubrication: Grease
【0022】この試験条件と、を比較すると、本発
明の試験条件は高荷重、高速、過酷な潤滑条件になって
いることが分かる。すなわち、本発明における試験条件
は境界潤滑条件になっている。試験の結果、以下の摩耗
量(体積摩耗量、mm3 )、および焼付時間(オイルカ
ット後焼付に至るまでの時間−分)が得られた。Comparing these test conditions, it can be seen that the test conditions of the present invention are high load, high speed, and severe lubrication conditions. That is, the test conditions in the present invention are boundary lubrication conditions. As a result of the test, the following abrasion amount (volume abrasion amount, mm 3 ) and baking time (time from oil cut to baking-min) were obtained.
【0023】 摩耗量(mm3 ) 焼付時間(分) 発明例A MoS2 25wt% 0.08 55 グラファイト25wt% ポリアミドイミド50wt% 発明例B MoS2 40wt% 0.1 60 グラファイト 10wt% ポリアミドイミド50wt% 比較例1 MoS2 50wt% 0.9 50 ポリアミドイミド50wt% 比較例2 グラファイト 50wt% 0.08 20 ポリアミドイミド50wt% 比較例3 MoS2 10wt% 0.3 16 グラファイト 10wt% ポリアミドイミド80wt% Amount of wear (mm 3 ) Baking time (min) Inventive Example A 25 wt% of MoS 2 0.08 55 25 wt% of graphite 50 wt% of Inventive Example B MoS 2 40 wt% 0.160 10 wt% of graphite 50 wt% of polyamide imide Comparative Example 1 MoS 2 50 wt% 0.9 50 Polyamide imide 50 wt% Comparative Example 2 Graphite 50 wt% 0.08 20 Polyamide imide 50 wt% Comparative Example 3 MoS 2 10 wt% 0.3 16 Graphite 10 wt% Polyamide imide 80 wt%
【0024】さらに以下の試験条件で試験を行った。 耐焼付性試験 荷重:10kg 速度:4m/sec 潤滑:5分間ミスト潤滑後ミスト供給をカット 油種:パラフィン油 速度:4m/sec 試験時間:2時間Further, the test was performed under the following test conditions. Seizure resistance test Load: 10 kg Speed: 4 m / sec Lubrication: Cut off mist supply after mist lubrication for 5 minutes Oil type: paraffin oil Speed: 4 m / sec Test time: 2 hours
【0025】 [0025]
【0026】以上の試験結果より二硫化モリブデンとグ
ラファイトを併用し、その量を50%と多くした発明例
では優れた耐摩耗性が得られていることが分かる。続い
て、上記発明例Aの摺動材料につき焼結層露出率を変化
させた試験片を作成し、耐焼付性、耐摩耗性および摩擦
係数を測定した。ただし試験条件は、油種を冷凍機油1
対軽油9の混合油とし、潤滑はミスト5分給油後給油を
カットする方法とし、その他の試験条件は上記のものと
同じとした。From the above test results, it can be seen that excellent abrasion resistance is obtained in the invention examples in which molybdenum disulfide and graphite are used in combination and the amount is increased to 50%. Subsequently, test pieces were prepared by changing the exposure rate of the sintered layer with respect to the sliding material of Inventive Example A, and the seizure resistance, wear resistance and coefficient of friction were measured. However, the test condition was that the oil type was refrigeration oil 1
A mixed oil of light oil 9 was used, lubrication was performed by lubricating the oil after cutting for 5 minutes, and other test conditions were the same as those described above.
【0027】耐焼付性試験結果を図1に示す。図1よ
り、焼結層露出率が95%を超えると耐焼付性が急激に
劣化することが分かる。また焼結層露出率が80%以下
では耐焼付性が安定していることが分かる。耐摩耗性試
験結果を図2に示す。焼結層露出率が約10%より低い
と、樹脂や固体潤滑剤が脱落しやすいために摩耗量が多
くなり、一方焼結層露出率が約90%より多いと焼付傾
向が表れるために摩耗量が多くなっている。摩擦係数の
測定結果を図3に示す。焼結層露出率が約10%より低
いと、樹脂が崩れるように脱落するために摩擦係数が高
くなり、一方焼結層露出率が約90%より多いと摩耗量
が多くなるにともない、摺動面積が増加し、面圧が低下
して、潤滑条件が流体潤滑に近付くために摩擦係数が低
下している。FIG. 1 shows the results of the seizure resistance test. FIG. 1 shows that the seizure resistance rapidly deteriorates when the sintered layer exposure rate exceeds 95%. Further, it can be seen that the seizure resistance is stable when the sintering layer exposure rate is 80% or less. FIG. 2 shows the results of the wear resistance test. If the exposure ratio of the sintered layer is lower than about 10%, the resin or the solid lubricant tends to fall off, resulting in a large amount of wear. The amount is increasing. FIG. 3 shows the measurement results of the coefficient of friction. If the sintering layer exposure rate is lower than about 10%, the resin will fall off so as to collapse, resulting in a higher friction coefficient. On the other hand, if the sintering layer exposure rate is higher than about 90%, the amount of wear will increase as the amount of wear increases. The dynamic area increases, the surface pressure decreases, and the coefficient of friction decreases because the lubrication conditions approach fluid lubrication.
【0028】続いて焼付試験を行った後の試験片の表面
を観察したところ、樹脂と固体潤滑剤(以下これらを総
称して「樹脂組成物」という)が青銅焼結層表面および
軸表面に付着していること、および固体潤滑剤が30%
以上であると30%未満の場合に比較して付着量が著し
く多くなることが分かった。この結果につき考察する。
厳しい摺動条件では摩擦面での発熱が多くなり、そのた
め青銅よりも線膨張係数の大きい樹脂組成物が焼結層表
面よりも飛び出し、次に焼結層上に流動し、付着したも
のと推定される。固体潤滑剤が30%よりもすくないと
樹脂の結合力が高いために、固体潤滑剤が摺動剤表面で
流動し、付着する状況が作りだされ難い。一方固体潤滑
剤が70%よりも多いと、樹脂の結合力が低下するため
に、固体潤滑剤の付着よりも摩耗の方が優先的に起こ
り、耐摩耗性が低下する。なお、焼結空孔に樹脂が充填
されていない材料では、樹脂成分と焼結金属の熱膨張係
数の相違を利用した樹脂組成物の飛び出しは望めず、ま
た焼結層へのグラファイトや二硫化モリブデンの付着力
は弱いために本発明例の材料よりも耐摩耗性及び耐焼付
性が劣っているものと考えられる。After observing the surface of the test piece after the baking test, the resin and the solid lubricant (hereinafter collectively referred to as “resin composition”) were applied to the surface of the bronze sintered layer and the surface of the shaft. 30% solid and solid lubricant
It was found that when the amount was more than the above, the amount of adhesion was remarkably increased as compared with the case of less than 30%. Let us consider this result.
It is presumed that heat generation on the friction surface increases under severe sliding conditions, so that the resin composition having a higher linear expansion coefficient than bronze spills out from the surface of the sintered layer and then flows and adheres to the sintered layer. Is done. If the solid lubricant is less than 30%, the bonding strength of the resin is high, so that it is difficult to create a situation in which the solid lubricant flows and adheres to the surface of the sliding agent. On the other hand, if the amount of the solid lubricant is more than 70%, since the bonding strength of the resin is reduced, abrasion occurs preferentially over the adhesion of the solid lubricant, and the wear resistance is reduced. In the case of a material in which the sintered pores are not filled with the resin, it is not possible to expect the resin composition using the difference in the coefficient of thermal expansion between the resin component and the sintered metal, and the graphite or disulfide to the sintered layer is not expected. It is considered that the abrasion resistance and seizure resistance are inferior to those of the material of the present invention because molybdenum has a weak adhesive force.
【0029】さらに固体潤滑剤の物性と上記したごとき
耐摩耗性・耐焼付性改良との関連につき考察する。二硫
化モリブデン(MoS2 )は一般にグラファイトに比べ
て粒径が小さい六方晶系の結晶であり、へき開しやす
い。したがって、焼結層表面に付着した二硫化モリブデ
ンは軸との摩擦によって剪断され、へき開し、さらに微
細な粒子となって、軸と摺動材料の間を潤滑する。しか
しながらこのような性質ゆえに、二硫化モリブデンの耐
摩耗性はグラファイトよりも劣っている(比較例1参
照)。一方、グラファイトは六方晶系の結晶であり、へ
き開しやすい点は二硫化モリブデンと同じであるが、硬
度が二硫化モリブデンよりも高く、粒径も大であるため
に樹脂との結合力が高いために、耐摩耗性を高める(比
較例2参照)。したがって二硫化モリブデンとグラファ
イトを併用することによって耐焼付性と耐摩耗性の両方
を良好にすることができる。特に、二硫化モリブデンと
グラファイトの合計使用量がそれぞれの単独使用量と同
じでも併用した方が相乗効果によって耐焼付性と耐摩耗
性を良好にすることができる(実施例A,Bと比較例
1、2参照)。以下、実施例により本発明を詳しく説明
する。Further, the relationship between the physical properties of the solid lubricant and the improvement in wear resistance and seizure resistance as described above will be discussed. Molybdenum disulfide (MoS 2 ) is generally a hexagonal crystal having a smaller particle size than graphite and is easily cleaved. Therefore, the molybdenum disulfide adhering to the surface of the sintered layer is sheared by friction with the shaft, cleaved, becomes fine particles, and lubricates between the shaft and the sliding material. However, due to such properties, the wear resistance of molybdenum disulfide is inferior to that of graphite (see Comparative Example 1). On the other hand, graphite is a hexagonal crystal and has the same cleavage points as molybdenum disulfide, but its hardness is higher than molybdenum disulfide and its particle size is larger, so its binding strength with resin is higher. Therefore, the wear resistance is enhanced (see Comparative Example 2). Therefore, by using molybdenum disulfide and graphite in combination, both seizure resistance and wear resistance can be improved. In particular, even when the total amount of molybdenum disulfide and graphite used is the same as the amount used alone, it is possible to improve the seizure resistance and abrasion resistance by a synergistic effect (Examples A and B and Comparative Examples 1, 2). Hereinafter, the present invention will be described in detail with reference to examples.
【0030】[0030]
【実施例】表1に示す組成につき上記した方法により摺
動部材を作成し、上記方法により耐摩耗性及び耐焼付性
を測定した結果を表に示す。摺動部材の物性は以下のと
おりであった。 摺動層厚み: 200μm 空孔率: 35%(体積) 焼結層露出率: 70%(面積) 焼結金属粒子粒径: 110μm(平均)EXAMPLES A sliding member was prepared by the above-described method using the composition shown in Table 1, and the abrasion resistance and seizure resistance were measured by the above-mentioned method. The physical properties of the sliding member were as follows. Sliding layer thickness: 200 μm Porosity: 35% (volume) Sintering layer exposure rate: 70% (area) Sintered metal particle diameter: 110 μm (average)
【0031】[0031]
【表1】 [Table 1]
【0032】[0032]
【表2】 [Table 2]
【0033】[0033]
【表3】 [Table 3]
【0034】[0034]
【発明の効果】以上の説明、特に実施例より明らかなよ
うに、本発明の摺動材料は厳しい摺動条件において優れ
た耐摩耗性及び耐焼付性を発揮する。As is apparent from the above description, particularly from the examples, the sliding material of the present invention exhibits excellent wear resistance and seizure resistance under severe sliding conditions.
【図1】焼結層露出率と焼付時間の関係を示すグラフで
ある。FIG. 1 is a graph showing a relationship between an exposure rate of a sintered layer and a baking time.
【図2】焼結層露出率と摩耗量の関係を示すグラフであ
る。FIG. 2 is a graph showing a relationship between an exposure rate of a sintered layer and a wear amount.
【図3】焼結層露出率と摩擦係数の関係を示すグラフで
ある。FIG. 3 is a graph showing a relationship between an exposure rate of a sintered layer and a friction coefficient.
【図4】焼結層露出率と切削量の関係を示すグラフであ
る。FIG. 4 is a graph showing a relationship between an exposure rate of a sintered layer and a cutting amount.
【図5】球状銅系粉末から構成される焼結層を示す金属
顕微鏡写真である。FIG. 5 is a metal micrograph showing a sintered layer composed of a spherical copper-based powder.
【図6】異形銅系粉末から構成される焼結層を示す金属
顕微鏡写真である。FIG. 6 is a metal micrograph showing a sintered layer composed of a deformed copper-based powder.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI C10M 103:04 103:06 103:00 103:02 107:38 107:32 107:44) C10N 10:02 10:08 10:12 20:00 20:06 30:06 40:02 50:08 (72)発明者 壁谷 泰典 愛知県豊田市緑ケ丘3丁目65番地 大豊 工業株式会社内 (72)発明者 島崎 敬一 愛知県豊田市緑ケ丘3丁目65番地 大豊 工業株式会社内 (56)参考文献 特公 昭63−37445(JP,B2) (58)調査した分野(Int.Cl.7,DB名) F16C 33/10 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification code FI C10M 103: 04 103: 06 103: 00 103: 02 107: 38 107: 32 107: 44) C10N 10:02 10:08 10: 12 20:00 20:06 30:06 40:02 50:08 (72) Inventor Yasunori Kabuya 3-65 Midorigaoka, Toyota City, Aichi Prefecture Inside Taitoyo Kogyo Co., Ltd. (72) Inventor Keiichi Shimazaki 3 Midorigaoka, Toyota City, Aichi Prefecture Chome 65, Taitoyo Kogyo Co., Ltd. (56) References JP-B-63-37445 (JP, B2) (58) Fields investigated (Int. Cl. 7 , DB name) F16C 33/10
Claims (2)
またはCu合金焼結層と、この焼結層の焼結粒子間の空
間に充填された合成樹脂及び固体潤滑剤とを含んでな
り、前記焼結層及び充填物質の表面を機械加工してなる
摺動材料において、前記焼結層は、2層以上に積層され
た粒径が30〜200μmの金属粒子を5〜70体積%
の空孔率で焼結した焼結金属からなり、かつ前記機械加
工された表面における焼結層の表面露出率が95%以下
であり、前記固体潤滑剤は合計量で30〜80重量%の
二硫化モリブデンとグラファイトからなり、混合潤滑又
は境界潤滑条件で摺動特性が優れた摺動材料。1. A back metal and Cu sintered on the surface of the back metal
Or a Cu alloy sintered layer, comprising a synthetic resin and a solid lubricant filled in the space between the sintered particles of the sintered layer, the surface of the sintered layer and the filling material is machined In the sliding material, the sintered layer is formed by stacking two or more layers of metal particles having a particle size of 30 to 200 μm in a volume of 5 to 70% by volume.
The sintered layer has a porosity of not more than 95%, and the surface exposure of the sintered layer on the machined surface is 95% or less, and the solid lubricant has a total amount of 30 to 80% by weight. A sliding material consisting of molybdenum disulfide and graphite and having excellent sliding characteristics under mixed lubrication or boundary lubrication conditions.
またはCu合金焼結層と、この焼結層の焼結粒子間の空
間に充填された合成樹脂及び固体潤滑剤とを含んでな
り、前記焼結層及び充填物質の表面を機械加工してなる
摺動材料において、前記焼結層は、2層以上に積層され
た粒径が30〜200μmの金属粒子を5〜70体積%
の空孔率で焼結した焼結金属からなり、かつ前記機械加
工された表面における焼結層の表面露出率が95%以下
であり、前記固体潤滑剤は合計量で30〜80重量%の
二硫化モリブデンおよびグラファイトと、3〜20重量
%の二硫化タングステン、BN、ふっ素樹脂、およびP
bの1種以上とからなり、混合潤滑又は境界潤滑条件で
摺動特性が優れた摺動材料。2. A back metal and Cu sintered on the surface of the back metal.
Or a Cu alloy sintered layer, comprising a synthetic resin and a solid lubricant filled in the space between the sintered particles of the sintered layer, the surface of the sintered layer and the filling material is machined In the sliding material, the sintered layer is formed by stacking two or more layers of metal particles having a particle size of 30 to 200 μm in a volume of 5 to 70% by volume.
The sintered layer has a porosity of not more than 95%, and the surface exposure of the sintered layer on the machined surface is 95% or less, and the solid lubricant has a total amount of 30 to 80% by weight. Molybdenum disulfide and graphite, 3-20% by weight of tungsten disulfide, BN, fluororesin, and P
A sliding material comprising at least one kind of b and having excellent sliding characteristics under mixed lubrication or boundary lubrication conditions.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/831,249 US5217814A (en) | 1991-02-09 | 1992-02-07 | Sintered sliding material |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3782091 | 1991-02-09 | ||
JP3-37820 | 1991-10-09 | ||
JP3-290578 | 1991-10-09 | ||
JP29057891 | 1991-10-09 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH05157115A JPH05157115A (en) | 1993-06-22 |
JP3003889B2 true JP3003889B2 (en) | 2000-01-31 |
Family
ID=
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