JPS6350381A - Carbonaceous abrasive material - Google Patents

Carbonaceous abrasive material

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Publication number
JPS6350381A
JPS6350381A JP19249786A JP19249786A JPS6350381A JP S6350381 A JPS6350381 A JP S6350381A JP 19249786 A JP19249786 A JP 19249786A JP 19249786 A JP19249786 A JP 19249786A JP S6350381 A JPS6350381 A JP S6350381A
Authority
JP
Japan
Prior art keywords
friction
carbonaceous
materials
coefficient
impregnated
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.)
Pending
Application number
JP19249786A
Other languages
Japanese (ja)
Inventor
岩城 英彦
植村 武夫
村上 繁
羽沢 均
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.)
Resonac Holdings Corp
Original Assignee
Showa Denko KK
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 Showa Denko KK filed Critical Showa Denko KK
Priority to JP19249786A priority Critical patent/JPS6350381A/en
Publication of JPS6350381A publication Critical patent/JPS6350381A/en
Pending legal-status Critical Current

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Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Abstract] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は炭素材に、比較的融点の低い金属無磯化合物を
含浸させた、低速度rfl擦係数の大きい炭素質摩擦材
に関する。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a carbonaceous friction material having a large low-speed rfl friction coefficient, which is obtained by impregnating a carbon material with a metal-free compound having a relatively low melting point.

〔従来の技術〕[Conventional technology]

′g擦材、特にブレーキ材は摩擦特性が浸れていること
は勿論のこと、摩擦熱を充分吸収できる熱容量を有し、
かつ軽量であることが要求される。
'gFriction materials, especially brake materials, not only have excellent friction properties, but also have a heat capacity that can sufficiently absorb frictional heat.
It is also required to be lightweight.

特に、航空機、レーシングカー等では、非常に苛酷な条
件で使用されるだけでなく、少しでb軽い材料が求めら
れている。
In particular, materials such as aircraft and racing cars are not only used under extremely harsh conditions, but also require materials that are slightly lighter.

炭素質摩擦材は、苛酷な条件でも摩擦係数が低下ぜず、
むしろ高くなり、熱容量が大きく、比重が軽い等の長所
を右し、この目的には最適であるが、強度が弱いのが欠
点であり、割れが発生したりして安全上の問題が生ずる
だけでなり、rP、耗が多く、実用化に難点があった。
Carbonaceous friction materials have a friction coefficient that does not decrease even under harsh conditions.
On the contrary, it has advantages such as high heat capacity, low specific gravity, etc., and is ideal for this purpose, but its disadvantage is that it is weak in strength, and it only causes safety problems such as cracking. Therefore, there was a lot of rP and wear, making it difficult to put it into practical use.

そのため、炭素繊維で補強(いわゆる炭素u1帷/炭素
避合材、以下C−C複合材という)することが行なわれ
るように41つ、強度も向上し、実用可能な程度に摩耗
も減少した。炭素質摩擦材は摩耗以外の性能が優れてい
るので、摩耗を減少する上記改良により烏性能摩擦材と
して、航空機、レーシングカー等にも利用されている。
For this reason, reinforcement with carbon fibers (so-called carbon lining/carbon insulation material, hereinafter referred to as C-C composite material) has improved the strength and reduced wear to a practical level. Since carbonaceous friction materials have excellent performance other than wear, they are also used in aircraft, racing cars, etc. as high-performance friction materials due to the above-mentioned improvements to reduce wear.

しかし、炭素質摩擦材は、優れた特性を有し、苛酷な条
件で高い摩擦係数を示すが、逆にゆるやかな条件では摩
擦係数が若干低い欠点がある。特に停止時の摩擦係数、
いわゆる静由t?tl係数が低く、パーキングブレーキ
としての性能が不十分である。
However, although carbonaceous friction materials have excellent properties and exhibit a high coefficient of friction under severe conditions, they have the disadvantage that the coefficient of friction is somewhat low under gentle conditions. Especially the coefficient of friction when stopping,
The so-called Shizuyu t? The tl coefficient is low and the performance as a parking brake is insufficient.

従来、摩擦特性を調整するためには、FJ擦拐に対応し
た種々な摩擦調整材が用いられている。例えば、レジン
系の摩擦材においては、右n系のゴム、カシュ、無代質
系の黒鉛、アルミナ、シリカ、金属系の鉄、銅、アルミ
ニウム等が用いられる。
Conventionally, in order to adjust friction characteristics, various friction adjustment materials have been used that are compatible with FJ abrasion. For example, in a resin-based friction material, right-n type rubber, cashew, free graphite, alumina, silica, metallic iron, copper, aluminum, etc. are used.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

ところで、炭素質摩擦材は1000℃以上の高温で焼成
して製造されるため、はとんどの摩擦調整材は変質した
り揮散したりしてしまうので、一般に使用されている摩
擦調整材は、炭素質摩擦材の原料に添加して使用するこ
とが出来ない。
By the way, since carbonaceous friction materials are manufactured by firing at high temperatures of 1000°C or higher, most friction modifiers deteriorate or volatilize, so commonly used friction modifiers are It cannot be added to raw materials for carbonaceous friction materials.

本発明者等は炭素質摩擦材が多数の細字孔を有すること
に着目し、炭素材の成形時にFM擦調整材を配合するこ
とが出来なくとも、焼成した製品にこれを含浸ずれば摩
擦調整材としての効果が発揮されると考え、鋭意研究を
行ない、金属無機化合物が有効であることを発見した。
The present inventors focused on the fact that carbonaceous friction materials have a large number of fine pores, and even if it is not possible to blend FM friction adjustment material during molding of carbon materials, friction can be adjusted by impregnating the fired product with this material. Thinking that it would be effective as a material, they conducted extensive research and discovered that metal inorganic compounds are effective.

本発明は上記の発見に塁づいてなされたもので、低速時
の摩擦係数が、ft速時1′l!擦係数と同等、或はそ
れ以上の値を有する炭素質摩擦材を提供することを目的
とする。
The present invention was made based on the above discovery, and the friction coefficient at low speed is 1'l at ft speed! It is an object of the present invention to provide a carbonaceous friction material having a friction coefficient equal to or higher than the friction coefficient.

〔問題点を解決−ヂるための手段〕[Means for solving problems]

本発明は上記の目的を達成するためになされたもので、
イの要旨は、炭素材の網空孔中に、融点が200〜10
00℃の金属無機化合物を含浸させた炭素質1’J擦材
にある。
The present invention has been made to achieve the above objects,
The gist of B is that the melting point is between 200 and 10 in the network pores of the carbon material.
It is a carbonaceous 1'J rubbing material impregnated with a metal inorganic compound at 00°C.

〔発明の具体的構成および作用〕[Specific structure and operation of the invention]

以下本発明の詳細な説明する。 The present invention will be explained in detail below.

本発明に用いられる炭素材は、炭素質摩擦材で、例えば
、炭素LyA紺の織布、或は不織布のマットにピッチ、
樹脂等の結合材を含浸、圧着して焼成し、必要に応じて
黒鉛化したもの、炭素繊維の短繊維をピッチ、樹脂等の
結合材と混線、成形焼成し、必要に応じて黒鉛化したも
の、或はセルロース繊維等に熱硬化性樹脂を含浸し、こ
れを圧着、硬化、焼成し、必要に応じて黒鉛化したもの
など、公知のものがあげられる。
The carbon material used in the present invention is a carbonaceous friction material, for example, carbon LyA navy blue woven fabric or non-woven fabric mat with pitch,
Impregnated with a binder such as resin, pressed and fired, graphitized as necessary, short carbon fibers mixed with pitch, binder such as resin, shaped and fired, and graphitized as necessary. Known materials include those obtained by impregnating a thermosetting resin with a thermosetting resin, or cellulose fibers, which are then compressed, hardened, fired, and optionally graphitized.

上記セルロース繊¥1等に熱硬化性樹脂を含浸して製造
した炭素材はガラスカーボンと言われるもので、焼成時
間を調整することにより空孔率が調整可能である。また
、C−C複合材は含浸の繰返しで空孔率の調整が可能で
ある。摩擦材に使用される炭素材は、それ程多く細字孔
を右せず、通常10〜20%、多くとも30%で、S擦
調整材を含浸するのに適−1の細字孔を右づるものであ
る。
The carbon material produced by impregnating the above-mentioned cellulose fiber with a thermosetting resin is called glass carbon, and the porosity can be adjusted by adjusting the firing time. Furthermore, the porosity of the CC composite material can be adjusted by repeating impregnation. The carbon material used in the friction material does not have a large number of fine pores, usually 10 to 20%, at most 30%, which is suitable for impregnating the S friction adjusting material. It is.

また、r!J擦調整材として使用される金属無機化合物
として好ましいものは、■A族、rVA族、IB族の硫
化物、ハロゲン化物、シアン化物に多い。例えば、Sb
 203. Sb 83 、 Bi 203 。
Also, r! Preferred metal inorganic compounds used as the J friction modifier include sulfides, halides, and cyanides of the A, rVA, and IB groups. For example, Sb
203. Sb 83, Bi 203.

Bi F3 、Bi  13 、Sn O,、Sn s
、pb o。
Bi F3 , Bi 13 , Sn O,, Sn s
, pbo.

Pb F2 、 Pb Cu2 、 Pb 3r 2 
、 PI) 12 。
PbF2, PbCu2, Pb3r2
, PI) 12.

Cu CN、Cu Br 、Cu I、AgCJ。Cu CN, Cu Br, Cu I, AgCJ.

AU CN、A+J Sr 、AQ 2 Sがあげられ
るが、これら金属無機化合物の他にも、Pb Cr 0
4 。
Examples include AU CN, A+J Sr, and AQ 2 S, but in addition to these metal inorganic compounds, Pb Cr 0
4.

PbSO4・PbO,AOzTe、A(+3 POa 
PbSO4・PbO,AOzTe,A(+3POa
.

A(] 4 F20y 、AG PO3、KB508 
A(] 4 F20y, AG PO3, KB508
.

Qa s、Ca  (PO3)2 、TJBI’ 、T
i I。
Qa s, Ca (PO3)2, TJBI', T
i I.

Ti2 S、Ti233 、FeAS2.Tj Ia 
Ti2S, Ti233, FeAS2. Tj Ia
.

Ni As 、Ni S、V20S 、VF3 、[3
a 02 。
NiAs, NiS, V20S, VF3, [3
a02.

AS2 S3 、 MOO3、Li F、 Li 3 
POa等が有効で・ある。」二記金属無機化合物【よ、
1種のみならず、2種以上を混合使用してもよい。
AS2 S3, MOO3, Li F, Li 3
POa etc. are effective. ”2 metal inorganic compounds [yo,
You may use not only one type but also a mixture of two or more types.

金属無代化合物の中には、水に溶は易いものがあり、極
端な場合は潮解性を右する。水に溶は易いものは、空気
中の水分を吸収したり、水に濡れて流出したりするおそ
れがあり、本発明に使用することを避けなければならな
い。
Some metal-free compounds are easily soluble in water, and in extreme cases they may become deliquescent. Materials that are easily soluble in water should be avoided for use in the present invention because they may absorb moisture in the air or become wet with water and flow out.

また、炭素質摩擦材は、苛酷な条件で使用され、摩擦熱
によって含浸した摩擦調整材が分解することがある。従
って分解生成物も摩擦調整作用を右するものがよく、金
属無機化合物は分解後に金属が残り、上記機能を発揮す
る。
Furthermore, carbonaceous friction materials are used under severe conditions, and the impregnated friction modifier may decompose due to frictional heat. Therefore, the decomposition products should also have a friction-adjusting effect, and the metal inorganic compound remains as a metal after being decomposed and exhibits the above-mentioned function.

さらに、炭素材に含浸さゼるためには、溶融しなければ
ならないため、融点のあまり高いしのは不適当で、実用
的には1000℃以下でなければならない。融点が1o
oo℃以下のものtよ、摩擦熱で溶融し、f@擦而面薄
いフィルムをつくる。そのフィルムが低速での摩擦係数
を高める。8′+i速では、そのフィルムは溶融し、炭
素材が摩擦面にあられれ、高いrP擦係数が得られる。
Furthermore, in order to impregnate the carbon material, it must be melted, so it is inappropriate to have a melting point that is too high; practically, the melting point must be 1000° C. or lower. Melting point is 1o
Anything below 0°C melts due to frictional heat and forms a thin film when rubbed. The film increases the coefficient of friction at low speeds. At 8'+i speed, the film melts and carbon material is deposited on the friction surface, resulting in a high rP friction coefficient.

分解生成物が金属のものは、今風自体が低速の摩擦係数
を高める効果を有するので、分解しても性能は殆ど変わ
らない。
If the decomposition product is metal, the decomposition product itself has the effect of increasing the low-speed friction coefficient, so there is almost no change in performance even if it is decomposed.

しかし、融点が低すぎるものは、l熱で容易に溶融流出
するので、摩擦調整材としては不適当で、200℃以上
て゛あることが必要である。
However, if the melting point is too low, it will easily melt and flow out under lukewarm heat, making it unsuitable as a friction modifier, and the temperature must be 200°C or higher.

したがって、融点200〜1000℃の水に溶けにくい
金属無機化合物を含浸することによって、炭素質摩擦材
の低速におけるFJf!A係数を高めることが出来る。
Therefore, by impregnating a metal inorganic compound with a melting point of 200 to 1000°C that is difficult to dissolve in water, the FJf of the carbonaceous friction material at low speeds can be improved. The A factor can be increased.

〔実施例〕〔Example〕

次に実施例、比較例を示して本発明を説明する。 Next, the present invention will be explained by showing examples and comparative examples.

実施例1 市販工業用)戸紙を水とともにミキサーでよく撹拌した
ものに、1:1の重槍比で工・タノールに希釈したフェ
ノール樹脂を混合し、シートマシンで成形した。この成
形品の密度をnめるため、さらにフェノール樹脂を含浸
して焼成した。この焼成品の嵩密度は1.29/CId
であった。この嵩密度をさらに高くするため、フェノー
ル樹脂の含浸、焼成を繰返して、嵩密度1.f3!7 
/c−m’の焼成品とした。
Example 1 A phenolic resin diluted with alcohol and ethanol at a ratio of 1:1 was mixed with a phenol resin diluted with alcohol and ethanol at a ratio of 1:1 to a mixture of (commercially available industrial use) door paper and water, and then molded using a sheet machine. In order to reduce the density of this molded product, it was further impregnated with phenol resin and fired. The bulk density of this fired product is 1.29/CId
Met. In order to further increase this bulk density, impregnation with phenol resin and firing are repeated until the bulk density reaches 1. f3!7
/cm' was made into a fired product.

これを2700℃にて黒鉛化した。This was graphitized at 2700°C.

次いで、上記黒鉛化した炭素材をA−トクレーブに入れ
、真空ポンプて゛減圧して2 Torrに保持り“ると
ともにオートクレーブ中に組込lυだヒータで加熱した
。炭素材の温度が含浸させる金属無償化合物の融点より
約100℃高くなった時点で、溶融した各種金属化合物
をぞれぞれオートクレーブ内に注入し、アルゴンガスを
用いて30に’J/cmに加圧し、ぞれぞれの金属無償
化合物が含浸された炭素質摩擦材を得た。
Next, the graphitized carbon material was placed in an A-toclave, and the pressure was reduced to 2 Torr using a vacuum pump, and the temperature was heated using a lυ heater built into the autoclave. When the temperature reached approximately 100°C higher than the melting point of the compound, each of the molten metal compounds was injected into the autoclave and pressurized to 30'J/cm using argon gas. A carbonaceous friction material impregnated with a free compound was obtained.

このようにして得られた摩擦材を、百径200#×厚ざ
6Mのディスクと3!+gX45mのパッドに加工し、
慣性式摩耗試験を用いて、時速501y / hr、面
圧10Kg/ciおよび時3i1100に/hr、面圧
20に9/dおける摩擦係数を測定した。
The friction material obtained in this way was combined with a disk with a diameter of 200# and a thickness of 6M. Processed into a +gX45m pad,
Using an inertial wear test, the friction coefficient was measured at a speed of 501 y/hr, a surface pressure of 10 Kg/ci, and a speed of 3/hr of 1100 y/hr, a surface pressure of 20/9/d.

実施例2 長さ約5 cmのPAN系炭素楳雑をマット状にしたも
のを積層し、軟化点85℃のコールタールピッチを含浸
して板状に成形した。この成形品を焼成し、さらに]−
ルクールピッチの含浸、焼成をF4返し、嵩密度1.6
9 /l−m’とした。これを結晶格子定数が6.85
になるように黒鉛化した後、実施例1とJi71様に各
種金属無償化合物を含浸した。きらに、実施例1と同様
に加工し、慣性式l!!擦試験を行なった。
Example 2 A mat of approximately 5 cm long PAN-based carbon fibers was laminated, impregnated with coal tar pitch having a softening point of 85° C., and formed into a plate. This molded product is fired, and further]-
Impregnated with Lecoeur pitch, returned to F4 for firing, bulk density 1.6
9/l-m'. The crystal lattice constant of this is 6.85
After graphitizing to give the following properties, various metal-free compounds were impregnated as in Example 1 and Ji71. Kiran was processed in the same manner as in Example 1, and the inertia formula l! ! A rubbing test was conducted.

実施例3 実施例1で作成した各種パッドと鋳鉄(Fe12)製デ
ィスクとをそれぞれ組合せて慣性式摩擦試験を行った。
Example 3 An inertial friction test was conducted using a combination of the various pads prepared in Example 1 and a cast iron (Fe12) disk.

実施例4 実施例2で作成した各種パッドと鋳鉄(Fe12)製デ
ィスクとを(れぞれ組合せて慣性式摩擦試験をtiっだ
Example 4 The various pads prepared in Example 2 and cast iron (Fe12) disks were combined and subjected to an inertial friction test.

比較例1.2 実施例1および2の金属化合物を含浸していない、結晶
格子定数6.85に黒鉛化した試料について、実施例1
と同様に加工して、慣性摩擦試験を行なった。
Comparative Example 1.2 Regarding the graphitized sample with a crystal lattice constant of 6.85, which was not impregnated with the metal compound of Examples 1 and 2, Example 1
It was processed in the same manner as above and an inertia friction test was conducted.

実施例1,2.3.4において各種金属無機化合物を、
それぞれ含浸した摩擦材、および比較例1.2の摩擦材
の各条件における摩擦係数を第1表に示づ。
In Examples 1, 2.3.4, various metal inorganic compounds,
Table 1 shows the friction coefficients under various conditions for the impregnated friction materials and the friction materials of Comparative Example 1.2.

〔発明の効果〕〔Effect of the invention〕

以上述べたように本発明に係る炭素質摩擦材は、低速時
の摩擦係数が向上し、従来の炭素質摩擦材の欠点を完全
に解消コるものである。
As described above, the carbonaceous friction material according to the present invention has an improved coefficient of friction at low speeds, completely eliminating the drawbacks of conventional carbonaceous friction materials.

Claims (1)

【特許請求の範囲】[Claims] 炭素材の細空孔中に、融点が200〜1000℃の金属
無機化合物を含浸させたことを特徴とする炭素質摩擦材
A carbonaceous friction material characterized in that a metal inorganic compound having a melting point of 200 to 1000°C is impregnated into the pores of the carbon material.
JP19249786A 1986-08-18 1986-08-18 Carbonaceous abrasive material Pending JPS6350381A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP19249786A JPS6350381A (en) 1986-08-18 1986-08-18 Carbonaceous abrasive material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19249786A JPS6350381A (en) 1986-08-18 1986-08-18 Carbonaceous abrasive material

Publications (1)

Publication Number Publication Date
JPS6350381A true JPS6350381A (en) 1988-03-03

Family

ID=16292289

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19249786A Pending JPS6350381A (en) 1986-08-18 1986-08-18 Carbonaceous abrasive material

Country Status (1)

Country Link
JP (1) JPS6350381A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04258643A (en) * 1991-02-14 1992-09-14 Shinto Paint Co Ltd Coated polyolefin molding
JPH05117549A (en) * 1991-02-14 1993-05-14 Daikyo Inc Undercoating composition
US5514735A (en) * 1992-02-13 1996-05-07 Daikyo Co., Ltd. Under-coating compositions of chlorinated polyolefins and epoxy resins
US8158715B2 (en) 2006-04-05 2012-04-17 Toyo Boseki Kabushiki Kaisha Binder resin composition

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04258643A (en) * 1991-02-14 1992-09-14 Shinto Paint Co Ltd Coated polyolefin molding
JPH05117549A (en) * 1991-02-14 1993-05-14 Daikyo Inc Undercoating composition
US5514735A (en) * 1992-02-13 1996-05-07 Daikyo Co., Ltd. Under-coating compositions of chlorinated polyolefins and epoxy resins
US8158715B2 (en) 2006-04-05 2012-04-17 Toyo Boseki Kabushiki Kaisha Binder resin composition

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