JPH0753947A - Wet friction material - Google Patents

Wet friction material

Info

Publication number
JPH0753947A
JPH0753947A JP22073293A JP22073293A JPH0753947A JP H0753947 A JPH0753947 A JP H0753947A JP 22073293 A JP22073293 A JP 22073293A JP 22073293 A JP22073293 A JP 22073293A JP H0753947 A JPH0753947 A JP H0753947A
Authority
JP
Japan
Prior art keywords
friction
powder
weight
friction material
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.)
Granted
Application number
JP22073293A
Other languages
Japanese (ja)
Other versions
JP3485270B2 (en
Inventor
Minoru Fukazawa
稔 深沢
Hidekazu Nishii
英一 西井
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Tokai Carbon Co Ltd
Original Assignee
Tokai Carbon Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Tokai Carbon Co Ltd filed Critical Tokai Carbon Co Ltd
Priority to JP22073293A priority Critical patent/JP3485270B2/en
Publication of JPH0753947A publication Critical patent/JPH0753947A/en
Application granted granted Critical
Publication of JP3485270B2 publication Critical patent/JP3485270B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

PURPOSE:To obtain the material made of a metallic sinter which material has an excellent energy absorption performance and always retains stable high- friction characteristics. CONSTITUTION:The material is obtained by sintering a bronze mixture comprising 20-35wt.% C, 2-8wt.% Sn, 4-10wt.% SiO2, up to 8wt.% Zn as an optional component, and Cu as the remainder, the C being in the form of a graphite powder having an average particle diameter of 20-60mum, a content of particles with diameters of 5-100mum of 90% or greater, and a graphite crystal plane distance, C0, of 0.672nm or shorter. The sinter is highly effective when it has a porosity of 15-20vol.% and a strength of 20MPa or greater.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、ブレーキパッドあるい
はクラッチフェーシングとして好適な優れたエネルギー
吸収能と高摩擦性能を備える焼結金属系の湿式摩擦材料
に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a sintered metal-based wet friction material suitable for a brake pad or a clutch facing and having excellent energy absorption and high friction performance.

【0002】[0002]

【従来の技術】相対する摩擦面間に潤滑油などの液体が
介在する状態で使用される湿式摩擦材料は、ブレーキパ
ッドやクラッチフェーシングとして有用されている。こ
の湿式摩擦材料には、ペーパー系、ゴム系などのものも
あるが、現状では主に耐熱性および機械的強度に優れる
焼結金属系が用いられている。
2. Description of the Related Art Wet friction materials used with a liquid such as lubricating oil interposed between opposing friction surfaces are useful as brake pads and clutch facings. There are paper-based and rubber-based wet friction materials, but at present, mainly sintered metal-based materials having excellent heat resistance and mechanical strength are used.

【0003】焼結金属系の湿式摩擦材料としては、従来
からCuを主成分としSn、Zn、Al、Al2 3
SiO2 、MoS2 等を添加した組成成分を焼結した銅
合金系材質のものが主流となっているが、これら金属お
よびセラミック粉末に加えて黒鉛その他の炭素質粉末を
有効成分として添加する試みがなされている。すなわ
ち、黒鉛は本来的に優れた潤滑性と熱的・化学的安定性
を備えているため従来から摩擦材料のフィラーとして用
いられてきた(例えば特開昭61−67736 号公報)が、炭
素質物の添加による一層の材質改善を図ったものとし
て、摩擦調整材の一部もしくは全部を結晶格子定数C0
が6.75〜6.85のセミ黒鉛で構成することにより
潤滑性の温度影響を除いた摩擦材(特開昭64−49726 号
公報)、フィラーとして膨張黒鉛を含有する高弾性の摩
擦材料(特開平3−282028号公報)、黒鉛粉末を10〜
30wt%、気孔率が10〜20%のコークス粉末を3〜
15wt%含有し、残部が銅を主体とした金属成分粉末の
焼結体からなる安定した高摩擦係数を有する湿式摩擦材
料(特開平5−32955 号公報)などが提案されている。
As a wet friction material of a sintered metal type, conventionally, Cu, Sn, Zn, Al, Al 2 O 3 ,
Copper alloy-based materials obtained by sintering composition components containing SiO 2 , MoS 2, etc. are mainly used. Attempts to add graphite and other carbonaceous powders as effective components in addition to these metal and ceramic powders. Has been done. That is, since graphite has inherently excellent lubricity and thermal / chemical stability, it has been conventionally used as a filler for friction materials (for example, Japanese Patent Laid-Open No. 61-67736). as aimed at the further material improvement by addition of a portion of the friction modifier or all crystal lattice constant C 0
No. 6.75 to 6.85 of semi-graphite to eliminate the effect of temperature on lubricity (Japanese Patent Laid-Open No. 64-49726), and a highly elastic friction material containing expanded graphite as a filler ( JP-A-3-282028), graphite powder 10
3 wt% of coke powder with 30 wt% and porosity of 10-20%
There has been proposed a wet friction material (Japanese Patent Laid-Open No. 5-32955) having a stable high friction coefficient, which is composed of a sintered body of a metal component powder containing 15 wt% and the balance being copper.

【0004】[0004]

【発明が解決しようとする課題】本発明者らは、青銅系
焼結材からなる摩擦材料において特に摩擦時のエネルギ
ー吸収能と添加黒鉛粉末との関係に着目して鋭意研究を
重ねた結果、フィラー成分の組成比を特定範囲に設定
し、かつ特定性状の黒鉛粉末を添加すると優れたエネル
ギー吸収能を発揮する摩擦材料が得られることを確認し
た。
DISCLOSURE OF INVENTION Problems to be Solved by the Invention As a result of intensive studies conducted by the present inventors, in the friction material made of a bronze-based sintered material, focusing on the relationship between the energy absorption capacity during friction and the added graphite powder, It was confirmed that a friction material exhibiting excellent energy absorbing ability can be obtained by setting the composition ratio of the filler components to a specific range and adding graphite powder having specific properties.

【0005】本発明は前記に知見に基づいて開発された
もので、その目的は、優れたエネルギー吸収能を発揮
し、常に安定した高摩擦性能を保有する金属焼結系の湿
式摩擦材料を提供することにある。
The present invention was developed on the basis of the above-mentioned findings, and an object thereof is to provide a metal-sintered wet friction material exhibiting an excellent energy absorption ability and always having stable high friction performance. To do.

【0006】[0006]

【課題を解決するための手段】上記の目的を達成するた
めの本発明による湿式摩擦材料は、C:20〜30重量
%、Sn:2〜8重量%、SiO2 :4〜10重量%、
残部がCuからなり、前記Cが平均粒子径20〜60μ
m で粒子径5〜100μm の粒分が90%以上の粒子性
状を有し、かつ黒鉛結晶面間C0 の層間距離が0.67
2nm以下の黒鉛粉末である組成の青銅系成分を焼結して
なることを構成上の特徴とする。
Means for Solving the Problems The wet friction material according to the present invention for achieving the above object is C: 20 to 30% by weight, Sn: 2 to 8% by weight, SiO 2 : 4: 10% by weight,
The balance is made of Cu, and the C has an average particle diameter of 20 to 60 μm.
Grains having a particle size of 5 to 100 μm in m have a particle property of 90% or more, and the interlayer distance between graphite crystal planes C 0 is 0.67.
A structural feature is that a bronze-based component having a composition of 2 nm or less of graphite powder is sintered.

【0007】本発明の湿式摩擦材料は、Cuを主体と
し、これに特定範囲のC、SnおよびSiO2 を添加配
合したフィラー組成からなる。添加成分のうち、Snは
焼結時にCuに固溶して焼結を促進し、750〜850
℃範囲での焼結化を可能にすると共に焼結体の開気孔率
を増大させる成分となる。その配合量は2〜8重量%と
する必要があり、2重量%未満ではCuの焼結が困難と
なり、8重量%を越えるとSn成分の凝固偏析を生じて
摩擦性能を劣化させる原因となる。SiO2 は、耐摩耗
性を付与し、同時に相手部材を適度に削磨して新たな摩
擦面を露出させることにより摩擦性能を安定させる成分
となるもので、4〜10重量%の範囲で添加する。この
添加量が4重量%未満であると耐摩耗性および摩擦係数
が低下し、10重量%を越えると相手部材に対する削磨
性が増大し過ぎるうえ焼結体の強度低下を招く。
The wet friction material of the present invention is mainly composed of Cu, and has a filler composition in which C, Sn and SiO 2 in a specific range are added and blended. Among the added components, Sn is solid-dissolved in Cu at the time of sintering to promote sintering, and 750 to 850
It is a component that enables sintering in the range of ° C and increases the open porosity of the sintered body. The blending amount is required to be 2 to 8% by weight, and if it is less than 2% by weight, it becomes difficult to sinter Cu, and if it exceeds 8% by weight, solidification segregation of the Sn component occurs to cause deterioration of friction performance. . SiO 2 is a component that imparts wear resistance and at the same time stabilizes the friction performance by appropriately grinding the mating member to expose a new friction surface, and is added in the range of 4 to 10% by weight. To do. If the added amount is less than 4% by weight, the wear resistance and the friction coefficient decrease, and if the added amount exceeds 10% by weight, the abradability of the counterpart member increases too much and the strength of the sintered body decreases.

【0008】上記の青銅系成分には、必要に応じてZn
を8重量%以下の量比で添加することができる。Znは
Snと同様に焼結助剤および開気孔率形成剤として機能
する成分となる。このため、Sn量を多くした際には無
添加でもよいが、高価なSnの添加量を少なくしてZn
を添加することが良好な配合手段となる。しかし、Zn
の添加量が8重量%を上廻ると凝固偏析を生じて摩擦性
能の低下原因となる。
If necessary, the bronze-based component may include Zn.
Can be added in an amount ratio of 8% by weight or less. Similar to Sn, Zn is a component that functions as a sintering aid and an open porosity forming agent. Therefore, when the amount of Sn is increased, no addition may be made, but the amount of expensive Sn added is reduced to
Is a good compounding means. However, Zn
If the amount of addition of Al exceeds 8% by weight, solidification segregation occurs, which causes a decrease in friction performance.

【0009】C成分としては、平均粒子径が20〜60
μm の範囲にあり、粒子径5〜100μm の粒分含有率
が90%以上の粒子性状を有し、かつ黒鉛結晶を構成す
るC0 面間の層間距離が0.672nm以下の黒鉛化が進
んだ黒鉛粉末を選択使用し、20〜35重量%の量比で
添加する。粒子性状を前記の範囲に限定する理由は、平
均粒子径20〜60μm で粒子径5〜100μm の粒分
が90%以上の条件を満たす場合に優れたエネルギー吸
収能が付与され、安定した摩擦性能と高い材質強度の保
持が可能となるためである。例えば、5μm 未満の微細
黒鉛粉末が多くなるとCu合金マトリックスの結合を分
断して焼結体の強度低下を招き、逆に100μm を上廻
る粒分が多くなると摩擦係数が減退する。黒鉛結晶面間
0 の層間距離が0.672nm以下の黒鉛粉末を用いる
のは、この高黒鉛性が摩擦特性を安定化させるために不
可欠な要素となるからである。また、該黒鉛粉末の添加
量を20〜35重量%の範囲に設定するのは、20重量
%を下廻ると上記の諸効果が発揮されず、また35重量
%を越えると焼結体の強度ならびに摩擦係数の低下が生
じるためである。
The C component has an average particle size of 20 to 60.
The particle size is in the range of μm, the content of particles having a particle size of 5 to 100 μm is 90% or more, and the interlayer distance between C 0 planes constituting the graphite crystal is 0.672 nm or less. Graphite powder is selectively used and added in an amount ratio of 20 to 35% by weight. The reason why the particle properties are limited to the above range is that when the average particle size of 20 to 60 μm and the particle size of 5 to 100 μm satisfy the condition of 90% or more, excellent energy absorbing ability is imparted and stable friction performance is obtained. This makes it possible to maintain high material strength. For example, if the amount of fine graphite powder of less than 5 μm increases, the bond of the Cu alloy matrix will be broken and the strength of the sintered body will decrease, and conversely, if the amount of particles exceeding 100 μm increases, the friction coefficient will decrease. The graphite powder having an interlayer distance of C 0 between graphite crystal planes of 0.672 nm or less is used because this high graphitization property is an essential element for stabilizing the friction characteristics. Further, the addition amount of the graphite powder is set in the range of 20 to 35% by weight when the above effects are not exhibited below 20% by weight, and the strength of the sintered body is exceeded when it exceeds 35% by weight. In addition, the friction coefficient is reduced.

【0010】上記のフィラー要件に加えて、焼結体とし
ての開気孔率が15〜20容量%であり、抗折力が20
MPa以上の特性を保持することが好ましい。開気孔率
は介在する油を含浸担持するために有効な特性であり、
これが15容量%未満では油の含浸担持能力が不足し、
20容量%を越えると強度低下を生じる。また、抗折力
は実用性のある材質強度を保持する要件で、20MPa
以上、実用上は20〜60MPaの範囲に調整する。こ
れら開気孔率および抗折力の特性は、焼結体を得る際の
成形圧力、焼成温度等の条件制御によって付与すること
ができる。
In addition to the above filler requirements, the open porosity of the sintered body is 15 to 20% by volume and the transverse rupture strength is 20.
It is preferable to maintain the characteristics of MPa or more. Open porosity is a property effective for impregnating and supporting intervening oil,
If this is less than 15% by volume, the impregnating and carrying capacity of oil is insufficient,
If it exceeds 20% by volume, the strength will be reduced. In addition, the transverse rupture strength is a requirement to maintain practical material strength, and is 20 MPa.
As described above, in practical use, the pressure is adjusted within the range of 20 to 60 MPa. These characteristics of open porosity and transverse rupture strength can be imparted by controlling the conditions such as molding pressure and firing temperature when obtaining a sintered body.

【0011】本発明の湿式摩擦材料は、上記した青銅系
フィラー成分を焼結して構成されるが、この焼結体は次
のようにして製造することができる。まず、好ましくは
電解銅粉のようなCu粉末に、フィラー全量に対する配
合割合として2〜35重量%の黒鉛粉末、2〜8重量%
のSn粉末、4〜10重量%のSiO2 粉末および必要
に応じて8重量%以下のZn粉末を添加する。黒鉛粉末
は、黒鉛結晶面間C0の層間距離が0.672nm以下に
なるまで黒鉛化した黒鉛材を、平均粒子径が20〜60
μm で含有する粒子径5〜100μm の粒分が90%以
上になるように粉砕・分級したものを使用する。Sn粉
末およびZn粉末としては、粒度200メッシュ以下の
アトマイズド粉またはスタンプ粉を用いることが好まし
く、SiO2 粉末としては5〜50μm の微粉末を適用
することが望ましい。
The wet friction material of the present invention is formed by sintering the above-mentioned bronze-based filler component, and this sintered body can be manufactured as follows. First, preferably Cu powder such as electrolytic copper powder, graphite powder of 2 to 35 wt% as a blending ratio to the total amount of filler, 2 to 8 wt%
Sn powder, 4-10 wt% SiO 2 powder, and if necessary, 8 wt% or less Zn powder are added. The graphite powder is a graphite material graphitized until the interlayer distance between the graphite crystal planes C 0 becomes 0.672 nm or less, and the average particle size is 20 to 60.
What is pulverized and classified so that the content of particles having a particle diameter of 5 to 100 µm is 90% or more is used. As the Sn powder and the Zn powder, atomized powder or stamp powder having a particle size of 200 mesh or less is preferably used, and as the SiO 2 powder, it is desirable to apply fine powder of 5 to 50 μm.

【0012】上記の組成を有するフィラー成分は均一に
機械混合し、圧粉成形したのち加圧下に焼結処理する。
圧粉成形はフィラー成分を金型に充填し、100〜10
00MPaの範囲内で得られる焼結体の開気孔率を考慮
した加圧力を適用しておこなう。焼結処理は、1〜10
MPaの圧力を付与した状態で還元性もしくは不活性雰
囲気下750〜850℃の温度域で実施する。この際の
適用圧力および焼結温度範囲は、得られる焼結体に開気
孔率および材質強度のバランズを考慮して条件設定され
る。得られた焼結体は、最終的に摩擦材形状に沿う加工
を施して製品とする。
The filler component having the above composition is uniformly mechanically mixed, powder-molded, and then sintered under pressure.
In powder compacting, the mold is filled with a filler component, and 100 to 10
The pressure is applied in consideration of the open porosity of the sintered body obtained within the range of 00 MPa. Sintering process is 1-10
It is carried out in a temperature range of 750 to 850 ° C. under a reducing or inert atmosphere while applying a pressure of MPa. At this time, the applied pressure and the sintering temperature range are set in consideration of the open porosity and the range of material strength of the obtained sintered body. The resulting sintered body is finally processed into a product in accordance with the shape of the friction material.

【0013】[0013]

【作用】本発明に係る湿式摩擦材料によれば、C:20
〜35重量%、Sn:2〜8重量%、残部がCuからな
るか、これに必要に応じてZn:8重量%以下を配合し
た青銅系成分のフィラー組成が、焼結体に適度の気孔率
と実用範囲の材質強度を与え、同時に優れた耐摩耗性と
安定した摩擦性能ならびに相手材に対する適度の削磨性
を付与するために機能する。特にC成分として平均粒子
径20〜60μmで粒子径5〜100μm の粒分含有率
が90%以上の粒子性状を有し、かつ黒鉛結晶面間C0
の層間距離が0.672nm以下の黒鉛粉末を選択的に配
合することにより、摩擦時のエネルギー吸収能が増大
し、一層安定した高水準の摩擦特性を保持させることが
可能となる。
According to the wet friction material of the present invention, C: 20
˜35% by weight, Sn: 2 to 8% by weight, the balance being Cu, or Zn: 8% by weight or less if necessary, and a filler composition of a bronze-based component having appropriate pores in the sintered body. Rate and a material strength within a practical range, and at the same time functions to impart excellent wear resistance, stable friction performance, and appropriate abradability to the mating material. In particular, the C component has an average particle size of 20 to 60 μm, a particle size of 5 to 100 μm and a particle content of 90% or more, and has a graphite crystal plane C 0
By selectively blending graphite powder having an interlayer distance of 0.672 nm or less, the energy absorption capacity at the time of friction is increased, and it becomes possible to maintain a more stable and high level friction characteristic.

【0014】また、焼結体組織の開気孔率が15〜20
容量%で、抗折力が20MPaの特性は、介在する潤滑
油等の液体を気孔内部に含浸担持して摩擦時のエネルギ
ー吸収能を高める作用をなし、同時に実用的な材質強度
を保持して安定した摩擦性能が付与される。
Further, the open porosity of the sintered structure is 15 to 20.
The characteristic that the capacity is 20% and the transverse rupture strength is 20 MPa is that the liquid such as the intervening lubricating oil is impregnated and carried inside the pores to enhance the energy absorption capacity at the time of friction, while at the same time maintaining the practical material strength. Stable friction performance is given.

【0015】このような作用が相俟って、ブレーキパッ
ドあるいはクラッチフェーシングとした場合に常に安定
した高摩擦性能が発揮される。
In combination with such an action, stable high friction performance is always exhibited in the case of a brake pad or clutch facing.

【0016】[0016]

【実施例】以下、本発明の実施例を比較例と対比して具
体的に説明する。
EXAMPLES Examples of the present invention will be specifically described below in comparison with comparative examples.

【0017】実施例1〜11、比較例1〜12 Cu粉末(電解銅粉)に対しSn粉末(スタンプ粉、20
0#以下) 、Zn粉末(スタンプ粉、200#以下) 、SiO
2 粉末(珪石粉、平均粒径17μm )および特定性状を有
する黒鉛粉末からなるC粉末を、表1に示す割合で配合
し、V型混合機により20分間乾式混合して均質な混合
粉末を調製した。これら青銅系フィラーの混合粉末を外
径335mm、内径280mmのリング状金型に充填したの
ち、所定の圧力を適用して圧粉成形し、厚さ1.5mmの
円板成形体を得た。ついで、各成形体を鉄芯板の両面に
配置して所定の加圧力を付与しながら還元性雰囲気下で
所定温度に加熱焼結して摩擦材料を作製した。該摩擦材
料平面研削加工し、更に油溝として螺旋溝および放射溝
(中心から外側に両面で38本) を加工して摩擦板を得
た。
Examples 1 to 11 and Comparative Examples 1 to 12 Sn powder (stamp powder, 20 powder) to Cu powder (electrolytic copper powder)
(0 # or less), Zn powder (stamp powder, 200 # or less), SiO
C powder composed of 2 powders (silica stone powder, average particle size 17 μm) and graphite powder having specific properties was blended at the ratio shown in Table 1, and dry mixed by a V-type mixer for 20 minutes to prepare a homogeneous mixed powder. did. A mixed powder of these bronze-based fillers was filled in a ring-shaped die having an outer diameter of 335 mm and an inner diameter of 280 mm, and then a predetermined pressure was applied to perform powder compacting to obtain a disk molded body having a thickness of 1.5 mm. Next, each molded body was placed on both sides of the iron core plate and heated and sintered at a predetermined temperature in a reducing atmosphere while applying a predetermined pressure to produce a friction material. The friction material was subjected to surface grinding, and then spiral grooves and radial grooves (38 on both sides from the center to the outside) were processed as oil grooves to obtain a friction plate.

【0018】得られた各摩擦材料(焼結体)の開気孔率
および抗折力を測定し、成形および焼結条件と併せて表
2に示した。なお、開気孔率の測定は真空中で焼結体に
水を含浸させ、その含浸量から算出した。また、抗折力
の測定は焼結体から幅15mm、長さ35mmの試片を切り
出し、25mmのスパンによる3点曲げ法(試験速度2mm
/minによる破壊荷重測定)によった。
The open porosity and transverse rupture strength of each of the obtained friction materials (sintered body) were measured and shown in Table 2 together with molding and sintering conditions. The open porosity was measured by impregnating the sintered body with water in a vacuum and calculating the amount of impregnation. In addition, the transverse rupture strength was measured by cutting a test piece having a width of 15 mm and a length of 35 mm from the sintered body, and using a 3-point bending method with a span of 25 mm (test speed: 2 mm
/ min breaking load measurement).

【0019】[0019]

【表1】 [Table 1]

【0020】[0020]

【表2】 [Table 2]

【0021】次に、上記の各摩擦板につき、下記の条件
で慣性型試験機により摩擦試験をおこない、限界状況と
なった時点の周速、停止時間、限界数値、摩擦係数およ
び異常発生状況(焼付以外)を表3に示した。摩擦試験
条件;摩擦板(摩擦面積292.2cm2、有効半径0.1550m)を
各3枚用い、相手材としてS45Cを4枚使って交互に
組み合わせて摩擦面数6面とした。慣性モーメントを1
0.5kgfms2、係合い面圧を20kgf/cm2 にそれぞれ設
定し、周速を6.5m/s から0.8m/s づつ上昇してト
ルク波形の異常などの限界状況が発生するまで摩擦試験
をおこなった。潤滑油にはエンジン油〔三菱石油(株)
製、SAE#30〕を用い、油温70℃、供給油量20ml/c
m2.minとした。なお、周速は焼付きが発生した時点の周
速で、数値が大きいほど高負荷条件で使用できることを
示す。限界数値はエネルギー吸収量を見掛け上の摩擦面
積当たりの慣性体の回転運動エネルギーで示し、エネル
ギー吸収量を停止時間で除したエネルギー吸収工率の値
で示した場合に〔エネルギー吸収量(kgfm/cm2)×エネル
ギー吸収工率(kgfm/cm2/s)〕で算出した値であり、焼付
き発生時の負荷に相当する。したがって、数値が大きい
ほど焼付きなしに高負荷条件で使用し得ることを示す。
また、摩擦係数は周速10m/s 時のトルクから〔μ=T
/P×Z×R〕式(但し、Tはトルク、Pは総押付け
力、Zは摩擦面数、Rは有効半径)で算出した値で、大
きいほど摩擦性能が高いことを示すものである。
Next, a friction test was conducted on each of the above friction plates by an inertial tester under the following conditions, and the peripheral speed, the stop time, the limit value, the friction coefficient and the abnormality occurrence condition at the time of the limit condition ( (Except for baking) is shown in Table 3. Friction test conditions: Friction plates (friction area 292.2 cm 2 , effective radius 0.1550 m) were used for each 3 sheets, and 4 sheets of S45C were used as mating materials to alternately combine them to obtain 6 friction surfaces. 1 moment of inertia
Set 0.5kgfms 2 and the engaging surface pressure to 20kgf / cm 2 , respectively, and increase the peripheral speed from 6.5m / s by 0.8m / s to rub until a critical situation such as abnormal torque waveform occurs. The test was done. Engine oil [Mitsubishi Oil Corp.]
Manufactured by SAE # 30], oil temperature 70 ° C, oil supply 20ml / c
m 2 .min. The peripheral speed is the peripheral speed at the time of seizure, and the larger the value, the higher the load can be used. The limit value is indicated by the rotational kinetic energy of the inertial body per apparent friction area, and the energy absorption rate obtained by dividing the energy absorption amount by the stop time is the energy absorption amount (kgfm / kgfm / cm 2 ) × energy absorption work rate (kgfm / cm 2 / s)], which corresponds to the load when seizure occurs. Therefore, the larger the value is, the more it can be used under high load condition without seizure.
The friction coefficient is calculated from the torque at a peripheral speed of 10 m / s [μ = T
/ P × Z × R] (where T is torque, P is total pressing force, Z is the number of friction surfaces, and R is effective radius). The larger the value, the higher the friction performance. .

【0022】[0022]

【表3】 [Table 3]

【0023】表1〜表3を考察して明らかなとおり、実
施例による摩擦材料はいずれも吸収エネルギー限界数値
が高く、かつ比較的優れた摩擦係数を示している。しか
し、実施例10および11は焼結体の開気孔率が15容
量%を下廻っているため、摩擦特性が低下傾向を示し
た。これに対し、本発明の条件を外れる比較例では、限
界数値および摩擦係数が相対的に低く、焼付き現象以外
の異常発生も多く認められた。
As is clear from a consideration of Tables 1 to 3, the friction materials according to the examples all have high absorption energy limit values and relatively excellent friction coefficients. However, in Examples 10 and 11, since the open porosity of the sintered body was less than 15% by volume, the friction characteristics tended to deteriorate. On the other hand, in the comparative examples that deviate from the conditions of the present invention, the limit value and the coefficient of friction were relatively low, and many abnormalities other than the seizure phenomenon were recognized.

【0024】[0024]

【発明の効果】以上のとおり、本発明によれば特定配合
比率によりC、Sn、SiO2 (Zn)を配合したCu
を主体とする組成の青銅系成分をフィラーとし、このう
ちC成分を特定の粒子性状と黒鉛化度を有する黒鉛粉末
とした焼結体からなり、優れたエネルギー吸収能ならび
に高摩擦性能を備えた湿式摩擦材料を提供することがで
きる。したがって、高性能が要求されるブレーキバッド
あるいはクラッチフェーシングとして極めて有用であ
る。
As described above, according to the present invention, Cu containing C, Sn, and SiO 2 (Zn) in a specific mixing ratio is used.
The composition is mainly composed of a bronze-based component as a filler, and the C component as a graphite powder having a specific particle property and a specific graphitization degree. The sintered body has excellent energy absorption and high friction performance. A wet friction material can be provided. Therefore, it is extremely useful as a brake pad or clutch facing that requires high performance.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 C:20〜35重量%、Sn:2〜8重
量%、SiO2 :4〜10重量%、残部がCuからな
り、前記Cが平均粒子径20〜60μm で粒子径5〜1
00μm の粒分が90%以上の粒子性状を有し、かつ黒
鉛結晶面間C0の層間距離が0.672nm以下の黒鉛粉
末である組成の青銅系成分を焼結してなることを特徴と
する湿式摩擦材料。
1. C: 20 to 35% by weight, Sn: 2 to 8% by weight, SiO 2 : 4 to 10% by weight, the balance being Cu, said C having an average particle size of 20 to 60 μm and a particle size of 5 to 5. 1
A bronze-based component having a composition, which is a graphite powder having a particle content of 00 μm of 90% or more and an interlayer distance between graphite crystal planes C 0 of 0.672 nm or less, is sintered. Wet friction material.
【請求項2】 青銅系成分としてZn:8重量%以下を
添加した請求項1記載の湿式摩擦材料。
2. The wet friction material according to claim 1, wherein Zn: 8 wt% or less is added as a bronze-based component.
【請求項3】 開気孔率が15〜20容量%、抗折力が
20MPa以上である請求項1又は2記載の湿式摩擦材
料。
3. The wet friction material according to claim 1, which has an open porosity of 15 to 20% by volume and a transverse rupture strength of 20 MPa or more.
JP22073293A 1993-08-12 1993-08-12 Wet friction material Expired - Fee Related JP3485270B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP22073293A JP3485270B2 (en) 1993-08-12 1993-08-12 Wet friction material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP22073293A JP3485270B2 (en) 1993-08-12 1993-08-12 Wet friction material

Publications (2)

Publication Number Publication Date
JPH0753947A true JPH0753947A (en) 1995-02-28
JP3485270B2 JP3485270B2 (en) 2004-01-13

Family

ID=16755665

Family Applications (1)

Application Number Title Priority Date Filing Date
JP22073293A Expired - Fee Related JP3485270B2 (en) 1993-08-12 1993-08-12 Wet friction material

Country Status (1)

Country Link
JP (1) JP3485270B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0716247A1 (en) * 1994-12-08 1996-06-12 SINTERSTAHL Gesellschaft m.b.H. Synchronizing ring with sinter-bronze friction surface
JPH09112611A (en) * 1995-10-20 1997-05-02 Tokyo Yogyo Co Ltd Brake lining material for conveyor
JPH09112610A (en) * 1995-10-20 1997-05-02 Tokyo Yogyo Co Ltd Brake lining material for tilting motor
JPH09112609A (en) * 1995-10-20 1997-05-02 Tokyo Yogyo Co Ltd Brake lining material for crane motor

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0716247A1 (en) * 1994-12-08 1996-06-12 SINTERSTAHL Gesellschaft m.b.H. Synchronizing ring with sinter-bronze friction surface
JPH09112611A (en) * 1995-10-20 1997-05-02 Tokyo Yogyo Co Ltd Brake lining material for conveyor
JPH09112610A (en) * 1995-10-20 1997-05-02 Tokyo Yogyo Co Ltd Brake lining material for tilting motor
JPH09112609A (en) * 1995-10-20 1997-05-02 Tokyo Yogyo Co Ltd Brake lining material for crane motor

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