JPS592732B2 - Sintered alloy friction material - Google Patents
Sintered alloy friction materialInfo
- Publication number
- JPS592732B2 JPS592732B2 JP318877A JP318877A JPS592732B2 JP S592732 B2 JPS592732 B2 JP S592732B2 JP 318877 A JP318877 A JP 318877A JP 318877 A JP318877 A JP 318877A JP S592732 B2 JPS592732 B2 JP S592732B2
- Authority
- JP
- Japan
- Prior art keywords
- friction
- friction material
- sintered alloy
- weight
- wear
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000002783 friction material Substances 0.000 title claims description 21
- 229910045601 alloy Inorganic materials 0.000 title claims description 7
- 239000000956 alloy Substances 0.000 title claims description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 14
- 229910052581 Si3N4 Inorganic materials 0.000 claims description 8
- 239000002184 metal Substances 0.000 claims description 7
- 229910052751 metal Inorganic materials 0.000 claims description 7
- 229910052742 iron Inorganic materials 0.000 claims description 6
- 238000002844 melting Methods 0.000 claims description 5
- 230000008018 melting Effects 0.000 claims description 5
- 229910052698 phosphorus Inorganic materials 0.000 claims description 5
- 229910001632 barium fluoride Inorganic materials 0.000 claims description 4
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 3
- 229910052797 bismuth Inorganic materials 0.000 claims description 3
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 229910052738 indium Inorganic materials 0.000 claims description 3
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 claims description 3
- 150000002739 metals Chemical class 0.000 claims description 3
- 229910052718 tin Inorganic materials 0.000 claims description 3
- 239000000463 material Substances 0.000 description 17
- 230000000694 effects Effects 0.000 description 13
- 239000002245 particle Substances 0.000 description 11
- 230000013011 mating Effects 0.000 description 10
- 239000011159 matrix material Substances 0.000 description 9
- 238000005245 sintering Methods 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- 239000010959 steel Substances 0.000 description 6
- 229910000831 Steel Inorganic materials 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 4
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 4
- 229910001634 calcium fluoride Inorganic materials 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000011574 phosphorus Substances 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 239000010953 base metal Substances 0.000 description 2
- 229910052793 cadmium Inorganic materials 0.000 description 2
- 229910001567 cementite Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 229910002804 graphite Inorganic materials 0.000 description 2
- 239000010439 graphite Substances 0.000 description 2
- KSOKAHYVTMZFBJ-UHFFFAOYSA-N iron;methane Chemical compound C.[Fe].[Fe].[Fe] KSOKAHYVTMZFBJ-UHFFFAOYSA-N 0.000 description 2
- 230000001050 lubricating effect Effects 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 229910052711 selenium Inorganic materials 0.000 description 2
- 239000011669 selenium Substances 0.000 description 2
- -1 silicon nitride Chemical class 0.000 description 2
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 2
- 230000000087 stabilizing effect Effects 0.000 description 2
- 229910000851 Alloy steel Inorganic materials 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910000881 Cu alloy Inorganic materials 0.000 description 1
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- 229910005091 Si3N Inorganic materials 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 238000004663 powder metallurgy Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
Landscapes
- Braking Arrangements (AREA)
- Powder Metallurgy (AREA)
Description
【発明の詳細な説明】
本発明は焼結合金よりなる摩擦材料に関するものであっ
て、特にブレーキ装置の小型化に寄与する焼結摩擦材料
を提供するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a friction material made of a sintered alloy, and in particular provides a sintered friction material that contributes to miniaturization of brake devices.
近年各種のブレーキ装置が小型化される傾向にあり、特
に自転車用のブレーキはミニサイクル車の普及に伴って
、後輪に使用されるバンドブレーキやキャリバーブレー
キの小型化は急務とされている。In recent years, there has been a trend toward miniaturization of various types of brake devices, and in particular, with the spread of minicycle bicycle brakes, there is an urgent need to miniaturize band brakes and caliber brakes used for rear wheels.
従来(1)ウーブン材、ゴムモールド材あるいはレジン
モールド材の摩擦材料、(2)周知の銅系あるいは鉄系
の焼結摩擦材料、(3)熱処理を施こした鋼材例えばS
CM−21鋼(JIS規格)が使用されている。Conventional materials include (1) woven, rubber molded or resin molded friction materials, (2) well-known copper-based or iron-based sintered friction materials, and (3) heat-treated steel materials such as S.
CM-21 steel (JIS standard) is used.
しかし、これらの摩擦材は、ブレーキの小型化を目的と
して、ブレーキの制動面積を小さくして苛酷な条件で使
用する場合、それぞれ欠点を有する。However, each of these friction materials has drawbacks when used under severe conditions by reducing the braking area of the brake for the purpose of downsizing the brake.
例えば(1)の摩擦材料は安価で比較的摩擦係数は高い
特徴を有するが、耐熱性が劣り、単位制動面積当りの吸
収エネルギーが大きいことが要求される場合、使用に耐
え得るものでない。For example, the friction material (1) is inexpensive and has a relatively high coefficient of friction, but it has poor heat resistance and cannot be used when a large amount of absorbed energy per unit braking area is required.
(2)の摩擦材料は耐熱性および耐摩耗性に優れた特性
を有し、単位制動面積当りの吸収エネルギーも大きい特
徴を有するが摩擦係数が0.15〜0.40程度であり
、ブレーキの制動面積を小さくするのに限界があること
、ならびに、焼結摩擦材料は一般に加圧焼結法で製造さ
れることもあって、他の摩擦材料に比べ非常に高価で自
転車用の摩擦材料としてほとんど使用されていない。The friction material (2) has excellent heat resistance and wear resistance, and also has a large absorption energy per unit braking area, but has a friction coefficient of about 0.15 to 0.40, and has a Because there is a limit to reducing the braking area, and because sintered friction materials are generally manufactured using a pressure sintering method, they are very expensive compared to other friction materials, making them difficult to use as friction materials for bicycles. Hardly used.
(3)の熱処理を施こした鋼材、例えばSCM−21鋼
(JIS規格)は耐熱性を有し、比較的安価で現在小型
化を目的とした自転車用ブレーキの摩擦材料として実用
されている。Steel materials subjected to heat treatment (3), such as SCM-21 steel (JIS standard), have heat resistance, are relatively inexpensive, and are currently in practical use as friction materials for bicycle brakes aimed at downsizing.
しかし耐摩耗性が劣ることならびに相手材の摩耗が他の
摩擦材料に比べ大きい欠点がある。However, it has the disadvantage of poor wear resistance and greater wear on the mating material than other friction materials.
又摩擦係数が不安定なためブレーキ力が一定しないこと
および単位制動面積当りの吸収エネルギーが大きい使用
条件下では、焼付を生じやすいなどの問題があり、小型
化にも自ずから限界がある。Furthermore, there are problems such as the fact that the braking force is not constant due to the unstable coefficient of friction, and that seizure is likely to occur under usage conditions where the absorbed energy per unit braking area is large, and there is a limit to miniaturization.
本発明は、上述のような目的を満足する高い摩擦抵抗と
優れた耐摩耗性を有する摩擦材料であって、経済性も兼
ね備えた焼結摩擦材料を提供せんとするものである。The present invention aims to provide a sintered friction material that satisfies the above objects and has high frictional resistance and excellent wear resistance, and is also economical.
かかる発明材は次の様にして製造される。This invention material is manufactured as follows.
重量係でS i 3N4 、+ 8〜25係、P;0.
3〜1.5%、C;0.2〜1.5%、残部が鉄になる
ように、それぞれの粉末を配合し、これらをプレス成型
、焼結して作られる。Weight section S i 3N4, + 8-25 section, P; 0.
It is made by blending the respective powders so that 3 to 1.5%, C; 0.2 to 1.5%, and the balance is iron, and press-molding and sintering them.
(以下の引ま1べて重量係を示す)本材料はこのままで
も、優れた摩擦特性を有するものであるが、更にこれら
のマトリックス強度に潤滑性を有する鉛やインヂウム、
ビスマス、錫の如き低融点金属を総量で1〜6%、ある
いはCaF2、又はBaF2.LiFの1種もしくは2
種を総量で3〜8%、含有せしめ潤滑性を賦与すること
により摩擦係数を安定化し、相手材の摩耗量を低減せし
める。(The following sums indicate weight ratios) This material has excellent frictional properties as is, but it is also possible to add lead, indium, which has lubricity to the matrix strength,
A total amount of 1 to 6% of low melting point metals such as bismuth, tin, or CaF2, or BaF2. LiF type 1 or 2
By containing 3 to 8% of seeds in total and imparting lubricity, the coefficient of friction is stabilized and the amount of wear on the mating material is reduced.
以下、組成範囲等の選定理由を述べる。The reasons for selecting the composition range etc. will be described below.
周知の焼結合金摩擦材料は、通常鋼および銅合金または
鉄および鉄合金の基体となる金属マ) IJラックス鉛
や黒鉛等の滑らかな作動特性を与えるための潤滑性物質
、およびアルミナやシリカ等の硬質粒子で摩擦抵抗の保
持向上および耐摩耗性向上のための増摩擦性物質から構
成されている。Well-known sintered alloy friction materials include base metals, usually steel and copper alloys or iron and iron alloys, lubricating substances such as IJ lux lead and graphite to provide smooth operating characteristics, and alumina and silica. It is composed of hard particles and a friction-increasing substance to improve retention of frictional resistance and wear resistance.
窒イと硅素もアルミナやシリカ等の酸化物と同じように
高い硬さを有する硬質粒子で、摩擦係数の向上、および
耐摩耗性改善のため添加され、その添加量は8〜25係
が適切である。Nitrogen and silicon are hard particles that have high hardness like oxides such as alumina and silica, and are added to improve the coefficient of friction and wear resistance, and the appropriate amount is 8 to 25 parts. It is.
添加量が8係以下ではその効果が充分に発揮されず、摩
擦係数の向上、耐摩耗性改善の効果が少ない。If the amount added is less than 8 parts, the effect will not be fully exhibited, and the effect of improving the friction coefficient and wear resistance will be small.
添加量が25係以上では焼結材料自体の強度が弱められ
、耐摩耗性はかえって低下し、相手摩擦面の損耗が大き
くなる。If the amount added is 25 parts or more, the strength of the sintered material itself is weakened, the wear resistance is even lowered, and the wear on the mating friction surface is increased.
増摩擦動質であるアルミナやシリカ等の酸化物あるいは
窒化硅素の如き窒化物の硬質粒子は、摩擦係数や耐摩耗
性に大きく影響するが、その効果を発揮するには摩擦面
に分散する硬質粒子が基体となる金属マトリックスに保
持されて、脱落しないことが必要であるが、一般にこれ
らの硬質粒子はそれ自体脆弱であること、更には金属マ
トリックスとの焼結性が悪いことの理由により、金属マ
トリックスから脱落しやすく、硬質粒子の添加のみで必
ずしも十分な摩擦特性は発揮できず、かえって脱落した
硬質粒子は砥粒研摩作用により摩擦材自体の摩耗を著し
く増大させること、および相手摩擦面の損耗にも大きな
影響を与えるものである。Hard particles of oxides such as alumina and silica, or nitrides such as silicon nitride, which are friction-enhancing substances, have a large effect on the friction coefficient and wear resistance, but in order to exert their effect, it is necessary to disperse hard particles on the friction surface. It is necessary for the particles to be retained in the base metal matrix and not fall off, but generally these hard particles are themselves brittle and furthermore, they have poor sinterability with the metal matrix. They easily fall off from the metal matrix, and the addition of hard particles alone does not necessarily provide sufficient frictional properties.On the contrary, the hard particles that fall off significantly increase the wear of the friction material itself due to the abrasive abrasive action, and cause damage to the mating friction surface. This also has a large impact on wear and tear.
本発明はかかる欠点を改善するため、種々研究の結果、
燐の添加が金属マトリックスの鉄と、硬質粒子の窒化硅
素の反応を生じせしめるのに極めて有効であるこ吉を見
出した。In order to improve these drawbacks, the present invention has been made as a result of various researches.
Kokichi has discovered that the addition of phosphorus is extremely effective in causing a reaction between iron in the metal matrix and silicon nitride in the hard particles.
燐は粉末冶金では焼結性改善、強度および耐摩耗性改善
の目的でしばしは微量添加されるが、本発明の場合もマ
トリックスの強化のはかSi3N4粒子表面の一部にF
e−8i合金層を形成せしめることによりマトリックス
とSi3N、との結合性を著しく向上せしめる効果を有
する。In powder metallurgy, phosphorus is often added in small amounts for the purpose of improving sinterability, strength, and wear resistance, but in the present invention, phosphorus is also added to a part of the Si3N4 particle surface to strengthen the matrix.
Formation of the e-8i alloy layer has the effect of significantly improving the bonding between the matrix and Si3N.
Pの添加量が0.3%以下ではその効果が少なく、1.
5係以上添加した場合には粒界に燐化合物を析出し、却
って材質を脆化させるので範囲を0.3〜1.5係とす
る。If the amount of P added is less than 0.3%, the effect will be small; 1.
If it is added in a ratio of 5 or more, phosphorus compounds will precipitate at the grain boundaries and the material will become brittle, so the range should be 0.3 to 1.5.
本発明材の焼結温度は1050°C(好ましくは108
0℃)〜1230℃の間で選択されうる。The sintering temperature of the present invention material is 1050°C (preferably 108°C
0°C) to 1230°C.
焼結温度が1050℃以下の場合には、マトリックスと
Si3N4の反応が十分でなく、また12300C以上
では、反応生成物の主体となるFe−8iの液相を生じ
るため、5iaN+の分解が著しく促進され、耐摩耗性
はかえって低下すること、および寸法精度も悪くなり好
ましくない。When the sintering temperature is below 1050°C, the reaction between the matrix and Si3N4 is insufficient, and when the sintering temperature is above 12300°C, a liquid phase of Fe-8i, which is the main reaction product, is generated, so the decomposition of 5iaN+ is significantly accelerated. This is not preferable since the abrasion resistance is rather reduced and the dimensional accuracy is also deteriorated.
Si3N4粉末の粒度は一60メツシュから+350メ
ツシユの粒度範囲のものが最適である。The optimum particle size of the Si3N4 powder is in the range of 160 mesh to +350 mesh.
60メツシュ以上では過度に相手摩擦面とひつかき摩擦
を生じるため相手摩擦面を損耗させる。If the mesh is more than 60, excessive friction will be produced between the mating friction surface and the mating friction surface will be worn out.
また350メツシユ以下では焼結時のF e −8i
3N4の反応をコントロールすることがむつかしい。In addition, if the mesh is less than 350, Fe -8i during sintering
It is difficult to control the 3N4 reaction.
この傾向はSi3N4添加量の多いものほど、あるいは
焼結温度が高いほど顕著である。This tendency becomes more pronounced as the amount of Si3N4 added increases or as the sintering temperature increases.
Cは鉄中に固溶し、マトリックス強度を高めるとともに
、一部はセメンタイトとして析出し耐摩耗性を改善する
。C dissolves in solid solution in iron and increases matrix strength, and a portion of it precipitates as cementite to improve wear resistance.
0.2%以下ではその効果は不十分であり、1.5係以
上ではネットワーク状のセメンタイトを生じ、材質を脆
化させるので範囲を0.2〜1.5%とする。If it is less than 0.2%, the effect is insufficient, and if it is more than 1.5, network-like cementite is formed and the material becomes brittle, so the range is set to 0.2 to 1.5%.
Pbは剪断強度が低く、I n 、B 1 t S n
、Cd 、Se、などとともに潤滑性を有する金属で
あるが、摩擦作用の結果、摩擦面における鉛は一部溶融
状態となったり、酸化してPbOの形となり更にその潤
滑性を増し、摩擦材料と相手摩擦面との凝着現象を防ぐ
働きをして摩擦係数を安定にし、相手摩擦面の損耗を小
さくする効果を有する。Pb has low shear strength, I n , B 1 t S n
It is a metal that has lubricating properties along with Cd, Se, etc., but as a result of friction, some of the lead on the friction surface becomes molten or oxidizes into the form of PbO, which further increases its lubricity and improves the friction material. It has the effect of preventing adhesion between the friction surface and the mating friction surface, stabilizing the coefficient of friction, and reducing wear and tear on the mating friction surface.
1%以下ではその効果が小さく、6%以上では摩擦係数
が低下すること、および材質強度も低下するので範囲を
1〜6%とする。If it is less than 1%, the effect will be small, and if it is more than 6%, the friction coefficient will decrease and the material strength will also decrease, so the range is set to 1 to 6%.
融点が329℃の鉛以外に、271℃のビスマス、23
1℃の錫、150℃のインヂウム、3200Cのカドミ
ウム、220℃のセレンなとも鉛と同様の効果を発揮す
る。In addition to lead, which has a melting point of 329°C, bismuth, which has a melting point of 271°C, and 23
Tin at 1°C, indium at 150°C, cadmium at 3200°C, and selenium at 220°C exhibit the same effect as lead.
従ってこれらは一つ又は一つ以上、合計で1〜6係の範
囲の添加とするものである。Therefore, one or more of these may be added in a total amount of 1 to 6.
CaF2あるいはBaF2 、L s Fの潤滑性を有
する弗化物の添加は、Pb等の低融点金属と同様、摩擦
係数を安定にし相手摩擦面の損耗を小さくする効果を有
する。Addition of a lubricious fluoride such as CaF2, BaF2, or LsF has the effect of stabilizing the coefficient of friction and reducing wear on the mating friction surface, similar to low melting point metals such as Pb.
CaF2およびBaF2.LiFは摩擦中に非常によく
似た挙動を示すため、単独で加えてもよく、同時に2種
を添加してもよい。CaF2 and BaF2. Since LiF exhibits very similar behavior during friction, it may be added alone or two types may be added at the same time.
その添加量が合計3%以下では効果が小さく、8係以上
では材質強度が低下するため好ましい範囲を合計3〜8
チとした。If the amount added is less than 3% in total, the effect will be small, and if it is more than 8%, the material strength will decrease, so the preferred range is 3 to 8% in total.
It was hot.
次に実施例を述べる。Next, an example will be described.
実施例 1
一10o+3soメツシュのSi3N4粉末および一3
00メツシュの赤燐粉末、グラファイト、−150メツ
シユの鉄粉を表1の組成に配合し、5 t /cni圧
力で成型後1000℃、あるいは1150℃で30分還
元雰囲気中で焼結を行なって得られた焼結体を表2に示
す試験条件で摩擦摩耗試験を行なった。Example 1 -10o+3so mesh Si3N4 powder and -3
Red phosphorus powder of 00 mesh, graphite, and iron powder of -150 mesh were blended into the composition shown in Table 1, molded at 5 t/cni pressure, and then sintered at 1000°C or 1150°C for 30 minutes in a reducing atmosphere. The obtained sintered body was subjected to a friction and wear test under the test conditions shown in Table 2.
又現在実用されているSCM−21鋼(JIS規格)の
熱処理材および周知の焼結Cu系摩擦材(70%Cu7
%5n−7%C−7%Pb−9%5iO7組成)につい
ても比較のために試験した。In addition, the heat-treated SCM-21 steel (JIS standard) currently in use and the well-known sintered Cu-based friction material (70% Cu7
%5n-7%C-7%Pb-9%5iO7 composition) was also tested for comparison.
これらの試験結果を表3にまとめて示した。These test results are summarized in Table 3.
以上の結果より明らかなとおり、本発明材は高い摩擦力
と秀でた耐摩耗性を兼ね備えたすぐれた摩擦特性を有す
る。As is clear from the above results, the material of the present invention has excellent frictional properties that combine high frictional force and excellent wear resistance.
実施例 2
実施例1と同様に表4の組成に配合し、5t/m圧力で
成型後1150℃×30分焼結して得た試料を実施例1
と同様に表2に示す試験条件で摩擦摩耗試験を行ない、
その結果を表5に示した。Example 2 A sample obtained by blending the composition shown in Table 4 in the same manner as in Example 1, molding at 5 t/m pressure, and sintering at 1150°C for 30 minutes was prepared in Example 1.
Similarly, a friction and wear test was conducted under the test conditions shown in Table 2,
The results are shown in Table 5.
以上の結果から明らかなように、本発明品組成範囲のP
bあるいはCaF2を含有するものは、高い摩擦力と耐
摩耗性を有し、更には相手材の損耗を改善し図に示す如
く摩擦力の安定性を高める効果も発揮するものである。As is clear from the above results, P in the composition range of the product of the present invention
Those containing b or CaF2 have high frictional force and wear resistance, and also exhibit the effect of improving the wear of the mating material and increasing the stability of the frictional force as shown in the figure.
図は表2に示した条件で摩擦摩耗試験により得た摩擦力
測定線図の中、比較材および発明材の代表的なものを記
載したものである。
(タテ軸の摩擦力は6m=I5Kf−αである)The figure shows representative friction force measurement diagrams of comparative materials and invented materials among the friction force measurement diagrams obtained by friction and wear tests under the conditions shown in Table 2. (The frictional force on the vertical axis is 6m=I5Kf-α)
Claims (1)
.5条、C;0.2〜1,5饅、残部が実質的に鉄から
なる焼結合金摩擦材料。 2 重量係で3i3Nt;8〜25%、P;0.3〜1
.5%、C;0.2〜1.5%さらに鉛、インジウム、
ビスマス、錫などの低融点金属を少なくとも一種1〜6
重量係含有する焼結合金摩擦材料。 3 重量係で3 i3N458〜25%、P;0.3〜
1.5%、 C; 0.2〜1.5 %さらにCaF
2あるいはBaF2゜LiFの少なくとも一種3〜8重
量係含有する焼結合金摩擦材料。[Claims] 1 Si3N4 in terms of weight: 8 to 25 inches, P: 0.3 to 1
.. Article 5, C: Sintered alloy friction material consisting of 0.2 to 1.5 pieces and the remainder substantially iron. 2 Weight: 3i3Nt; 8-25%, P; 0.3-1
.. 5%, C; 0.2-1.5% plus lead, indium,
At least 1 to 6 types of low melting point metals such as bismuth and tin
Sintered alloy friction material containing weight ratio. 3 Weight: 3 i3N458~25%, P; 0.3~
1.5%, C; 0.2-1.5% further CaF
A sintered alloy friction material containing at least 3 to 8 parts by weight of at least one of 2 or BaF2°LiF.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP318877A JPS592732B2 (en) | 1977-01-14 | 1977-01-14 | Sintered alloy friction material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP318877A JPS592732B2 (en) | 1977-01-14 | 1977-01-14 | Sintered alloy friction material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5388610A JPS5388610A (en) | 1978-08-04 |
| JPS592732B2 true JPS592732B2 (en) | 1984-01-20 |
Family
ID=11550415
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP318877A Expired JPS592732B2 (en) | 1977-01-14 | 1977-01-14 | Sintered alloy friction material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS592732B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58110656A (en) * | 1981-12-25 | 1983-07-01 | Daido Steel Co Ltd | Composite material and its manufacture |
-
1977
- 1977-01-14 JP JP318877A patent/JPS592732B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5388610A (en) | 1978-08-04 |
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