JPH0726032A - Friction material - Google Patents

Friction material

Info

Publication number
JPH0726032A
JPH0726032A JP19317093A JP19317093A JPH0726032A JP H0726032 A JPH0726032 A JP H0726032A JP 19317093 A JP19317093 A JP 19317093A JP 19317093 A JP19317093 A JP 19317093A JP H0726032 A JPH0726032 A JP H0726032A
Authority
JP
Japan
Prior art keywords
friction
friction material
wear
octotitanate
resin
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
JP19317093A
Other languages
Japanese (ja)
Other versions
JP2958602B2 (en
Inventor
Isamu Kobayashi
勇 小林
Kenji Otsubo
憲司 大坪
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.)
Kubota Corp
Original Assignee
Kubota Corp
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 Kubota Corp filed Critical Kubota Corp
Priority to JP19317093A priority Critical patent/JP2958602B2/en
Publication of JPH0726032A publication Critical patent/JPH0726032A/en
Application granted granted Critical
Publication of JP2958602B2 publication Critical patent/JP2958602B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE:To improve the coefficient of friction and abrasion resistance of a friction material used for a brake of an automobile, etc. CONSTITUTION:A friction material is produced by molding a mixture comprising a binder resin and a base material comprising an octotitanate of a hollandite structure of the formula: KXBaYAlX+2YTi8-X-2YO16 (wherein X is 0.2-1.4; and Y is 0.2-1.4) in an amt. of about 3-50wt.%. Other known fibers may be used jointly. Suitable amts. of a friction-adjusting agent (e.g. barium sulfate) and other ingredients (e. g. a rust preventive) may be compounded if necessary.

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、自動車、鉄道車両,航
空機、産業機械類等の制動装置を構成するブレーキライ
ニング,ディスクパッド、クラッチッフェーシング等の
摺動部材として有用な摩擦材に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a friction material useful as a sliding member such as a brake lining, a disk pad, a clutch facing, etc., which constitutes a braking device for automobiles, railway vehicles, aircrafts, industrial machines and the like.

【0002】[0002]

【従来の技術】上記制動装置における摩擦材として、従
来よりアスベスト繊維を基材とし、これを樹脂結合剤
(フェノール樹脂,エポキシ樹脂等)に分散させ、必要
に応じ摩擦・摩耗調整剤(硫酸バリウム等)を添加した
混練物を加熱・加圧下に結着成形して製造される摩擦材
が使用されてきた。
2. Description of the Related Art As a friction material in the above-mentioned braking device, asbestos fiber has been used as a base material and dispersed in a resin binder (phenol resin, epoxy resin, etc.), and a friction / wear modifier (barium sulfate) is used as necessary. Friction materials produced by binding and molding a kneaded product to which is added under heat and pressure have been used.

【0003】[0003]

【発明が解決しようとする課題】自動車等の高速度化
や、ブレーキ装置の小型化・軽量化等に対処するために
は、摩擦係数が高く、その高摩擦係数が低温から高温に
亘る広い温度域で安定に維持され、かつ摩耗抵抗性にも
優れた摩擦材が要求される。アスベスト繊維を基材とす
る摩擦材は、摩擦摩耗特性に優れた摩擦材として使用さ
れてきたものであるが、摩擦面が高温化するに伴って摩
耗が著しく増大し、かつ高温域では摩擦係数が急激に低
下するフェード現象を生じる等、高温域における性能劣
化が大きい。また、摩擦摩耗特性に優れているとされる
低温域においても、摩擦係数は相対的に低く、上記要請
に対応し得るものではない。更に、近時はアスベスト繊
維の発がん性の問題が指摘され、環境衛生の見地から
も、その代替品の開発が要請されている。本発明は、上
記に鑑み、アスベスト繊維の使用を排すると共に、高速
度化や、ブレーキ装置の小型・軽量化等の要請に応える
ための改良された摩擦摩耗特性を有する摩擦材を提供し
ようとるものである。
In order to cope with higher speeds of automobiles and downsizing and weight reduction of brake devices, the coefficient of friction is high, and the high coefficient of friction has a wide temperature range from low temperature to high temperature. A friction material that is stably maintained in the region and has excellent abrasion resistance is required. Friction materials based on asbestos fibers have been used as friction materials with excellent friction and wear characteristics, but wear increases markedly as the friction surface becomes hot, and the friction coefficient at high temperatures increases. The performance deteriorates significantly in the high temperature range, such as a fade phenomenon in which the temperature rapidly decreases. Further, even in a low temperature range which is considered to have excellent friction and wear characteristics, the coefficient of friction is relatively low, and the above requirements cannot be met. Further, recently, the problem of carcinogenicity of asbestos fibers has been pointed out, and development of a substitute for the same has been demanded from the viewpoint of environmental hygiene. In view of the above, the present invention intends to provide a friction material which has improved friction and wear characteristics in order to eliminate the use of asbestos fibers and to meet the demands for higher speed and smaller and lighter brake devices. It is a thing.

【0004】[0004]

【課題を解決するための手段】本発明は、樹脂を結合剤
とし基材を含む混練物を結着成形してなる摩擦材におい
て、その基材として、次式〔1〕 Kx BaY Alx+2YTi8-X-2Y16 …〔1〕 〔式中,X は0.2 〜1.4 、Y は0.2 〜1.4 である〕で示
されるホランダイト型構造を有するオクトチタン酸塩が
3〜50重量%配合されていることを特徴としている。
DISCLOSURE OF THE INVENTION The present invention provides a friction material obtained by binding and molding a kneaded material containing a base material using a resin as a binder, and the base material has the following formula [1] K x Ba Y Al x + 2Y Ti 8-X-2Y O 16 [1] 3 to 50 parts by weight of octotitanate having a hollandite type structure represented by the formula [wherein X is 0.2 to 1.4 and Y is 0.2 to 1.4] It is characterized by being blended in%.

【0005】[0005]

【作用】上記〔1〕式で示されるホランダイト型構造を
有するオクトチタン酸塩の結晶は、(Ti,Al)O6
八面体のなす枠の中にK+ ,Ba++イオンが配位した一
次元トンネル構造を有する合成無機化合物である〔無機
材質研究所研究報告第57号 第4〜7頁「材料合成に
関する研究」〕。このものは高融点〔約1450℃以
上、例えばK0.7 Ba0.7 Al2.1 Ti5.9 16(X=Y=
0.7 )の融点は約1510℃〕を有し、耐熱性、補強効
果にすぐれ、またその硬さはモース硬度で約5〜6と、
摩擦材として適度の硬さを有している。自動車用ブレー
キパッド等の摩擦材の実使用において、その摩擦面は摩
擦熱の発生と蓄熱とにより、局部的に1000℃以上に
昇温すると推定される。このような苛酷な使用条件に曝
される摩擦材の基材として上記オクトチタン酸塩を配合
することにより、後記実施例に示すように、高温度域に
おいても卓抜した耐摩耗性と高い摩擦係数が確保され
る。その改良された摩擦摩耗特性の温度依存性は極めて
小さく、低温から高温に亘る広い温度域において安定に
維持される。
The crystal of octotitanate having the hollandite type structure represented by the above formula [1] is (Ti, Al) O 6
It is a synthetic inorganic compound having a one-dimensional tunnel structure in which K + and Ba ++ ions are coordinated in the frame formed by an octahedron [Inorganic Material Research Institute Research Report No. 57, pages 4 to 7 "Study on material synthesis" ]]. This has a high melting point [about 1450 ° C. or higher, for example, K 0.7 Ba 0.7 Al 2.1 Ti 5.9 O 16 (X = Y =
0.7) has a melting point of about 1510 ° C.] and has excellent heat resistance and reinforcing effect, and its hardness is about 5 to 6 in Mohs hardness,
It has an appropriate hardness as a friction material. In the actual use of a friction material such as an automobile brake pad, it is estimated that the friction surface locally heats up to 1000 ° C. or higher due to frictional heat generation and heat accumulation. By blending the octotitanate as the base material of the friction material exposed to such severe usage conditions, as shown in the examples below, the wear resistance and the high friction coefficient are excellent even in the high temperature range. Is secured. The temperature dependency of the improved friction and wear characteristics is extremely small, and is stably maintained in a wide temperature range from low temperature to high temperature.

【0006】以下、本発明の摩擦材について詳しく説明
する。本発明の摩擦材の基材であるオクトチタン酸塩の
配合割合は、摩擦摩耗特性改善効果を発現させるため
に、少なくとも3重量%を必要とする。しかし、その配
合量は50重量%までで十分であり、それを越えて多量
に配合する利益はない。このため、3〜50重量%とす
る。オクトチタン酸塩の形状は特に限定されないが、長
径:約10〜100μm,短径:約3〜20μm,アス
ペクト比:約2〜5の粒子形態を有するものは、樹脂中
への混練分散の均一性がよく、補強効果等に優れてい
る。また、アスベスト繊維を使用した摩擦材に指摘され
ているように、ブレーキ等の実使用時の摩擦面から発生
する粉塵中に、極微細片(断面径約1μm以下)が混在
することは環境衛生上有害であるとされているが、上記
粒サイズのものであれば、そのような極微細片が生じる
ことはなく、安全性も確保される。
Hereinafter, the friction material of the present invention will be described in detail. The blending ratio of octotitanate, which is the base material of the friction material of the present invention, needs to be at least 3% by weight in order to exert the effect of improving friction and wear characteristics. However, the blending amount is sufficient up to 50% by weight, and there is no advantage of blending a large amount beyond that. Therefore, the amount is 3 to 50% by weight. The shape of octotitanate is not particularly limited, but those having a particle morphology with a major axis of about 10 to 100 μm, a minor axis of about 3 to 20 μm, and an aspect ratio of about 2 to 5 are uniformly kneaded and dispersed in a resin. Excellent in reinforcing effect. In addition, as pointed out in friction materials that use asbestos fibers, it is a matter of environmental hygiene that dust particles generated from the friction surface during actual use such as brakes contain ultrafine particles (cross-sectional diameter of about 1 μm or less). Although it is said to be harmful, if the particles have the above-mentioned grain size, such ultrafine pieces will not occur, and safety can be secured.

【0007】本発明の摩擦材は、基材として、上記オク
トチタン酸塩と共に、公知の他種繊維、例えばポリアミ
ド(ナイロン)繊維,アラミド繊維,スチール繊維,ス
テンレス繊維,銅繊維,黄銅繊維,炭素繊維,ガラス繊
維,セラミックス繊維,ロックウール,木質パルプ等か
ら選ばれる1種〜2種以上の繊維を複合的に(例えば、
上記オクトチタン酸塩との合計量で約10〜65重量
%)使用してよい。上記基材は、必要に応じて、分散
性、結合剤樹脂との結着性の向上等のために、常法に従
ってシラン系カップリング剤(アミノシラン,ビニルシ
ラン,エポキシシラン,メタアクリロキシラン,メルカ
プトキシラン等)、またはチタネート系カップリング剤
(イソプロピルトリイソステアロイルチタネート,ジ
(ジオクチルパイロホスフェート)エチレンチタネート
等)による表面処理(カップリング処理)が施されて使
用される。
The friction material of the present invention, together with the octotitanate as the base material, other known fibers such as polyamide (nylon) fiber, aramid fiber, steel fiber, stainless fiber, copper fiber, brass fiber and carbon. One or more kinds of fibers selected from fibers, glass fibers, ceramic fibers, rock wool, wood pulp, etc. are combined (for example,
10 to 65% by weight in total with the octotitanate). The above-mentioned substrate is a silane coupling agent (aminosilane, vinylsilane, epoxysilane, methacryloxylan, mercapto) according to a conventional method for improving dispersibility, binding property with a binder resin, etc., if necessary. (Xylsilane, etc.) or a titanate-based coupling agent (isopropyl triisostearoyl titanate, di (dioctyl pyrophosphate) ethylene titanate, etc.) is used after being subjected to a surface treatment (coupling treatment).

【0008】本発明の摩擦材は、所望により、公知の摩
擦摩耗調整剤、例えば、加硫もしくは未加硫の天然・合
成ゴム粉末,カシュー樹脂粉粒体,レジンダスト,ゴム
ダスト等の有機物粉末、天然・人造黒鉛,二硫化モリブ
デン,三硫化アンチモン,硫酸バリウム,炭酸カルシウ
ム等の無機質粉末、銅,アルミニウム,亜鉛,鉄等の金
属粉末、アルミナ,シリカ,酸化クロム,酸化銅,三酸
化アンチモン,酸化チタン,酸化鉄等の酸化物粉末等か
ら選ばれる1種ないし2種以上の成分が、摩擦摩耗特性
(摩擦係数,摩耗抵抗性,振動特性,ナキ等)の改善を
目的として適量(例えば20〜70重量%)配合され
る。また、本発明の摩擦材は、各種添加剤、例えば防錆
剤、潤滑剤、研削剤等が、その用途・使用態様等に応じ
て適量配合(例えば50重量%以下)されることも通常
の摩擦材と異ならない。
If desired, the friction material of the present invention is a known friction and wear modifier, for example, vulcanized or unvulcanized natural / synthetic rubber powder, cashew resin powder, organic powder such as resin dust and rubber dust, Natural / artificial graphite, molybdenum disulfide, antimony trisulfide, inorganic powder such as barium sulfate, calcium carbonate, metal powder such as copper, aluminum, zinc, iron, alumina, silica, chromium oxide, copper oxide, antimony trioxide, oxidation One or more components selected from oxide powders such as titanium and iron oxide are used in an appropriate amount (for example, 20 to 20) for the purpose of improving friction and wear characteristics (friction coefficient, wear resistance, vibration characteristics, pear, etc.). 70% by weight). Further, in the friction material of the present invention, it is usual that various additives such as rust preventives, lubricants, abrasives, etc. are blended in an appropriate amount (for example, 50% by weight or less) in accordance with the application / use mode thereof. It is no different from friction material.

【0009】本発明の摩擦材における結合剤である樹脂
成分は、通常使用される材種、例えばフェノール樹脂,
ホルムアルデヒド樹脂,エポキシ樹脂,シリコーン樹脂
等の熱硬化性樹脂、またはこれらの変性(カシュー油変
性,乾性変性等)熱硬化性樹脂、天然ゴム、スチレンブ
タジエンゴム,ニトリルゴム等のゴム系樹脂等が挙げら
れる。
The resin component, which is the binder in the friction material of the present invention, is a commonly used material such as phenol resin,
Thermosetting resins such as formaldehyde resin, epoxy resin, silicone resin, thermosetting resins modified with these (cashew oil modification, dry modification, etc.), rubber-based resins such as natural rubber, styrene butadiene rubber, nitrile rubber, etc. To be

【0010】本発明の摩擦材は、基材として上記オクト
チタン酸塩を使用する点を除いて、その成分構成はアス
ベスト繊維等を基材とする従来の摩擦材と異ならず、ま
たその製造工程にも特別の条件の付加ないし制限は課せ
られない。すなわち、基材を結合剤樹脂中に分散し、必
要に応じて配合される摩擦摩耗調整剤、および防錆剤,
潤滑剤,研削剤等を添加し、均一に混練して原料組成物
を調製し、ついで金型成形等により、加熱・加圧下に結
着成形を行い、必要に応じて熱処理を施し、しかる後そ
の成形体に機械加工、研磨加工を加えて所定の形状を有
する摩擦材に仕上げる。別法として、原料組成物を、水
等に分散懸濁させ、抄き網で抄きあげ、搾水してシート
を抄造し、その適当枚数を重ね、加熱・加圧下に結着成
形し、成形体を機械加工,研磨加工して所定の摩擦材を
得る。
The friction material of the present invention has the same component composition as the conventional friction material having asbestos fibers as a base material except that the above-mentioned octotitanate is used as the base material, and the manufacturing process thereof. Is not subject to any special conditions or restrictions. That is, a base material is dispersed in a binder resin, and a friction and wear modifier and a rust preventive agent, which are blended as needed,
Lubricants, abrasives, etc. are added, and the mixture is uniformly kneaded to prepare a raw material composition, which is then subjected to binding molding under heat and pressure by die molding or the like, and heat treatment if necessary, and thereafter. Machining and polishing are applied to the molded body to finish the friction material having a predetermined shape. Alternatively, the raw material composition is dispersed and suspended in water or the like, made with a paper making net, squeezed with water to make a sheet, and an appropriate number of sheets are stacked, and binding molding is performed under heating and pressure, The molded body is machined and polished to obtain a predetermined friction material.

【0011】[0011]

【実施例】【Example】

〔供試摩擦材の製作〕基材としてオクトチタン酸塩〔K
0.7 Ba0.7 Al2.1 Ti5.9 16、X =Y=0.7 〕
(後記参考例による)を使用し、下記の原料組成物を調
製して金型による結着成形(加圧力:14.7MPa=150K
gf/cm 2 ,温度:170 ℃, 加圧保持時間:5 分間)を行
い、成形後、離型して乾燥炉で熱処理(180 ℃に3 時間
保持) を施す。その後、所定寸法に切断し、研磨加工を
加えて供試摩擦材( ディスクパッド) を得た。この摩擦
材をAとする。 基材 30重量% 結合剤樹脂(フェノール樹脂) 20重量% 摩擦調整剤(硫酸バリウム) 50重量%
[Production of test friction material] Octo titanate [K
0.7 Ba 0.7 Al 2.1 Ti 5.9 O 16 , X = Y = 0.7]
Using the following reference examples, prepare the following raw material compositions and bond molding with a die (pressing force: 14.7 MPa = 150 K)
gf / cm 2 , temperature: 170 ° C, pressurization holding time: 5 minutes), after molding, release and heat-treat in a drying oven (holding at 180 ° C for 3 hours). After that, it was cut into a predetermined size and subjected to polishing to obtain a test friction material (disk pad). This friction material is designated as A. Base material 30% by weight Binder resin (phenolic resin) 20% by weight Friction modifier (barium sulfate) 50% by weight

【0012】比較例 基材として、オクトチタン酸塩に代え、アスベスト繊維
(6クラス)を使用した点を除いて実施例1と同一の原
料組成、および製造工程により、供試摩擦材(ディスク
パッド)を得た。この摩擦材(従来タイプ)をBとす
る。
Comparative Example The friction material (disc pad) to be tested was prepared by the same raw material composition and production process as in Example 1 except that asbestos fibers (6 class) were used as the base material instead of octotitanate. ) Got. This friction material (conventional type) is designated as B.

【0013】〔摩擦摩耗試験〕上記摩擦材A(発明例)
およびB1(比較例)について、JIS D4411 「自動車用
ブレーキライニング」に規定の定速度摩擦摩耗試験によ
り、摩擦係数および比摩耗率(cm3 /N・m)を測定
し、図1および図2に示す結果を得た〔図1:摩擦係
数,図2:比摩耗率〕。 ディスク摩擦面:FC25ねずみ鋳鉄、 面圧:10Kgf/cm2 、摩擦速度:7m/ 秒。
[Friction and Wear Test] Above Friction Material A (Invention Example)
For B1 and B1 (comparative example), the friction coefficient and specific wear rate (cm 3 / N · m) were measured by the constant speed friction wear test specified in JIS D4411 “Brake lining for automobiles”. The obtained results were obtained [Fig. 1: friction coefficient, Fig. 2: specific wear rate]. Disc friction surface: FC25 gray cast iron, surface pressure: 10Kgf / cm 2 , friction speed: 7m / sec.

【0014】図1(摩擦係数)および図2(比摩耗率)
に示したように、アスベスト繊維を使用した摩擦材B
は、低温域および高温域での摩擦係数が低く、特に35
0℃を越える高温域での低下は急激である。耐摩耗性
も、高温化に伴って低下し、300℃を越える温度域に
おける劣化は顕著である。これに対し、発明例の摩擦材
Aは、高い摩擦係数を有し、かつその温度依存性は極め
て小さく、低温から高温に亘る広い温度域において高摩
擦係数が安定に維持され、耐摩耗性についても、低温域
はむろん、300℃を越える高温域での摩耗量の増加も
極く軽微であり、上記摩擦材Bの摩擦摩耗特性との差異
は歴然である。
FIG. 1 (friction coefficient) and FIG. 2 (specific wear rate)
As shown in, friction material B using asbestos fibers
Has a low coefficient of friction at low and high temperatures, especially 35
The drop in the high temperature region above 0 ° C is rapid. The wear resistance also decreases with increasing temperature, and the deterioration in the temperature range exceeding 300 ° C. is remarkable. On the other hand, the friction material A of the invention example has a high friction coefficient and its temperature dependence is extremely small, and the high friction coefficient is stably maintained in a wide temperature range from low temperature to high temperature, and the wear resistance is low. However, in the low temperature region, of course, the increase in the amount of wear in the high temperature region exceeding 300 ° C. is extremely small, and the difference from the friction and wear characteristics of the friction material B is obvious.

【0015】[0015]

【参考例】[Reference example]

〔ホランダイト型構造を有するオクトチタン酸塩の製
造〕 (1)原料組成物:炭酸カリウム、炭酸バリウム、酸化
アルミニウム、酸化チタンを、K2 CO3:BaC
3 :Al2 3 :TiO2 =0.7:1.4:2.
1:11.8のモル比に配合する。ミキサーで10分間
混合し、混合粉末に水5重量%を添加した後、型に充填
しプレス成形(加圧力5.1MPa)する。 (2)焼成処理:上記プレス成形体を焼成炉中、900
℃に2Hr保持して炭酸カリウム(K2CO3 )のCO
2 を離脱させた後、1350℃に3時間加熱保持して焼
成反応(固相反応に基づくオクトチタン酸塩の生成・育
成反応)を行わせ、ついで炉中冷却する。焼成反生成物
は、オクトチタン酸塩が固結した塊状物である。 (3)解繊処理:焼成反応生成物を粗粉砕し、2mm フル
イを全通させた後、水1Lを加え、家庭用ミキサーで1
0分間攪拌を加え湿式解繊する。解繊後、脱水乾燥す
る。 組成(X線粉末回折):K0.7 Ba0.7 Al2.1 Ti
5.9 16 サイズ(走査型電子顕微鏡):長径10〜50μm,短
径3〜20μm,アスペクト比2〜3。
[Production of octotitanate having hollandite type structure] (1) Raw material composition: potassium carbonate, barium carbonate, aluminum oxide, titanium oxide, K 2 CO 3 : BaC
O 3 : Al 2 O 3 : TiO 2 = 0.7: 1.4: 2.
It is mixed in a molar ratio of 1: 11.8. After mixing with a mixer for 10 minutes and adding 5% by weight of water to the mixed powder, the mixture is filled in a mold and press-molded (pressing pressure 5.1 MPa). (2) Firing treatment: 900 mm of the above press-molded body in a firing furnace
Keep 2Hr at ℃ for CO of potassium carbonate (K 2 CO 3 ).
After releasing 2 , the mixture is heated and held at 1350 ° C. for 3 hours to cause a firing reaction (octotitanate generation / growth reaction based on solid-phase reaction), and then cooled in the furnace. The calcined reaction product is a lump in which octotitanate is solidified. (3) Disentanglement treatment: The calcination reaction product was roughly crushed and passed through a 2 mm sieve, then 1 L of water was added and the mixture was mixed with a household mixer to 1
Stir for 0 minutes and wet defibration. After defibration, dehydration and drying. Composition (X-ray powder diffraction): K 0.7 Ba 0.7 Al 2.1 Ti
5.9 O 16 size (scanning electron microscope): major axis 10-50 μm, minor axis 3-20 μm, aspect ratio 2-3.

【0016】[0016]

【発明の効果】本発明の摩擦材は、高い摩擦係数と卓抜
した摩耗抵抗性を有している。その摩擦摩耗特性の温度
依存性は小さく、低温から高温にわたる広い温度域にお
いて安定に維持される。従って、本発明の摩擦材は、自
動車,車両,航空機,各種産業機械類等の制動装置のブ
レーキライニング,クラッチフェーシング,ディスクパ
ッド等として有用であり、高速度化、制動装置の小型・
軽量化等への対応を可能とし、また制動機能の向上・安
定化、耐久性向上等の効果を奏するものである。
The friction material of the present invention has a high coefficient of friction and outstanding wear resistance. The temperature dependence of the friction and wear characteristics is small, and it is stably maintained in a wide temperature range from low temperature to high temperature. Therefore, the friction material of the present invention is useful as a brake lining, a clutch facing, a disk pad, etc. of a braking device for automobiles, vehicles, aircrafts, various industrial machines, etc., and has a high speed and a small braking device.
It is possible to cope with weight reduction and the like, and also it is possible to improve and stabilize the braking function and improve durability.

【図面の簡単な説明】[Brief description of drawings]

【図1】定速度摩擦摩耗試験による摩擦係数の測定結果
を示すグラフである。
FIG. 1 is a graph showing the results of measuring a friction coefficient by a constant speed friction and wear test.

【図2】定速度摩擦摩耗試験による比摩耗率の測定結果
を示すグラフである。
FIG. 2 is a graph showing a measurement result of a specific wear rate by a constant speed friction wear test.

【符号の説明】[Explanation of symbols]

A:発明例、B:比較例。 A: invention example, B: comparative example.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 樹脂を結合剤とし基材を含む混練物を結
着成形してなる摩擦材において、基材として、次式
〔1〕 Kx BaY Alx+2YTi8-x-2Y16 …〔1〕 〔式中,X は0.2 〜1.4 、Y は0.2 〜1.4 である〕で示
されるホランダイト型構造を有するオクトチタン酸塩が
3〜50重量%配合されていることを特徴とする摩擦
材。
1. A friction material obtained by binding and molding a kneaded material containing a base material using a resin as a binder, wherein the base material has the following formula [1] K x Ba Y Al x + 2Y Ti 8-x-2Y O 16 ... [1] [wherein X is 0.2 to 1.4 and Y is 0.2 to 1.4], and 3 to 50% by weight of octotitanate having a hollandite type structure is blended. Friction material
JP19317093A 1993-07-07 1993-07-07 Friction material Expired - Fee Related JP2958602B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP19317093A JP2958602B2 (en) 1993-07-07 1993-07-07 Friction material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19317093A JP2958602B2 (en) 1993-07-07 1993-07-07 Friction material

Publications (2)

Publication Number Publication Date
JPH0726032A true JPH0726032A (en) 1995-01-27
JP2958602B2 JP2958602B2 (en) 1999-10-06

Family

ID=16303464

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19317093A Expired - Fee Related JP2958602B2 (en) 1993-07-07 1993-07-07 Friction material

Country Status (1)

Country Link
JP (1) JP2958602B2 (en)

Also Published As

Publication number Publication date
JP2958602B2 (en) 1999-10-06

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