JPH10330732A - Friction material composition and friction material made therefrom - Google Patents
Friction material composition and friction material made therefromInfo
- Publication number
- JPH10330732A JPH10330732A JP14635897A JP14635897A JPH10330732A JP H10330732 A JPH10330732 A JP H10330732A JP 14635897 A JP14635897 A JP 14635897A JP 14635897 A JP14635897 A JP 14635897A JP H10330732 A JPH10330732 A JP H10330732A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- friction material
- silicon carbide
- weight
- fibers
- 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
Links
- 239000002783 friction material Substances 0.000 title claims abstract description 31
- 239000002131 composite material Substances 0.000 title 1
- 239000000203 mixture Substances 0.000 claims abstract description 23
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 claims abstract description 16
- 229910010271 silicon carbide Inorganic materials 0.000 claims abstract description 16
- 229910021397 glassy carbon Inorganic materials 0.000 claims abstract description 14
- 238000010438 heat treatment Methods 0.000 claims description 8
- 239000000835 fiber Substances 0.000 abstract description 17
- 229920005989 resin Polymers 0.000 abstract description 15
- 239000011347 resin Substances 0.000 abstract description 15
- 239000003795 chemical substances by application Substances 0.000 abstract description 12
- 229920001187 thermosetting polymer Polymers 0.000 abstract description 7
- 239000005011 phenolic resin Substances 0.000 abstract description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 5
- 239000011230 binding agent Substances 0.000 abstract description 5
- 239000000428 dust Substances 0.000 abstract description 4
- 239000000945 filler Substances 0.000 abstract description 4
- 238000000227 grinding Methods 0.000 abstract description 4
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 abstract description 4
- 239000000314 lubricant Substances 0.000 abstract description 4
- 239000012783 reinforcing fiber Substances 0.000 abstract description 4
- 229920001971 elastomer Polymers 0.000 abstract description 3
- 239000007849 furan resin Substances 0.000 abstract description 3
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 abstract description 3
- 244000226021 Anacardium occidentale Species 0.000 abstract description 2
- 239000004640 Melamine resin Substances 0.000 abstract description 2
- 229920000877 Melamine resin Polymers 0.000 abstract description 2
- 235000020226 cashew nut Nutrition 0.000 abstract description 2
- 239000003822 epoxy resin Substances 0.000 abstract description 2
- 239000003365 glass fiber Substances 0.000 abstract description 2
- 239000010439 graphite Substances 0.000 abstract description 2
- 229910002804 graphite Inorganic materials 0.000 abstract description 2
- 235000010299 hexamethylene tetramine Nutrition 0.000 abstract description 2
- 239000004312 hexamethylene tetramine Substances 0.000 abstract description 2
- 238000002156 mixing Methods 0.000 abstract description 2
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 abstract description 2
- 229920000647 polyepoxide Polymers 0.000 abstract description 2
- YPMOSINXXHVZIL-UHFFFAOYSA-N sulfanylideneantimony Chemical compound [Sb]=S YPMOSINXXHVZIL-UHFFFAOYSA-N 0.000 abstract description 2
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 abstract description 2
- 229920006337 unsaturated polyester resin Polymers 0.000 abstract description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 abstract 2
- 229920001568 phenolic resin Polymers 0.000 abstract 2
- 239000002241 glass-ceramic Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 230000002159 abnormal effect Effects 0.000 description 6
- 229910001369 Brass Inorganic materials 0.000 description 4
- 229910000831 Steel Inorganic materials 0.000 description 4
- 239000010951 brass Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000000465 moulding Methods 0.000 description 4
- 239000010959 steel Substances 0.000 description 4
- 238000005087 graphitization Methods 0.000 description 3
- 229910010272 inorganic material Inorganic materials 0.000 description 3
- 239000011147 inorganic material Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000004760 aramid Substances 0.000 description 2
- 229920006231 aramid fiber Polymers 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 239000012784 inorganic fiber Substances 0.000 description 2
- 230000037303 wrinkles Effects 0.000 description 2
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 description 1
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- GEIAQOFPUVMAGM-UHFFFAOYSA-N ZrO Inorganic materials [Zr]=O GEIAQOFPUVMAGM-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000003082 abrasive agent Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 238000003763 carbonization Methods 0.000 description 1
- 238000010000 carbonizing Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 239000002557 mineral fiber Substances 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920003987 resole Polymers 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Braking Arrangements (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、自動車、鉄道車
両、各種産業機械等の制動に用いられるディスクブレー
キパッド、ブレーキライニング等の摩擦材に適した摩擦
材組成物及び該摩擦材組成物を用いた摩擦材に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a friction material composition suitable for a friction material such as a disc brake pad and a brake lining used for braking automobiles, railway vehicles, various industrial machines, and the like, and to use of the friction material composition. Friction material.
【0002】[0002]
【従来の技術】自動車、鉄道車両、各種産業機械等に
は、その制動のためディスクブレーキパッド、ブレーキ
ライニング等の摩擦材が使用されている。この摩擦材と
して、従来は特開昭64−87930号公報、特開平2
−117985号公報等に示されるようにスチール繊維
を主構成繊維としたセミメタリック系摩擦材が主流であ
ったが、自動車産業界の軽量化、高級化への移行に沿っ
て、オートマチック車の発進時や停止時の異音発生、低
温での制動力不足、摩耗粉によるホイール汚れ等の問題
点が出て来た。ここで発生する異音は、速度が30km/
時間程度から減速していく過程で現われる摩擦材の制動
に伴うノイズ(70dB以上の音圧)であり、周波数では
約100(Hz)の乗用者に不快を感ずる領域の音であ
る。2. Description of the Related Art Friction materials such as disc brake pads and brake linings are used in automobiles, railway vehicles, various industrial machines and the like for braking. Conventionally, as this friction material, Japanese Patent Application Laid-Open No.
As shown in JP-A-117985, semi-metallic friction materials containing steel fibers as a main constituent fiber were the mainstream, but automatic vehicles were launched in line with the shift to lighter and more sophisticated automobile industries. Problems such as generation of abnormal noise at the time of stoppage and stoppage, insufficient braking force at low temperatures, and wheel contamination due to abrasion powder have come up. The abnormal noise generated here has a speed of 30 km /
This is noise (sound pressure of 70 dB or more) associated with braking of the friction material that appears in the process of decelerating from about time, and is a sound of a frequency of about 100 (Hz) in a region where a passenger feels discomfort.
【0003】これらの問題点を解消するため、スチール
繊維の代替として銅繊維、黄銅繊維等の非鉄金属繊維、
アラミド繊維、セラミック繊維等の有機繊維や無機繊
維、さらに安定した摩擦係数(μ≧0.38)を得るた
めに無機材料の研削剤を使用したノンスチール摩擦材へ
の移行が急速に進んできた。[0003] In order to solve these problems, non-ferrous metal fibers such as copper fiber and brass fiber are used instead of steel fiber.
The transition to non-steel friction materials using abrasives of inorganic materials in order to obtain organic fibers and inorganic fibers such as aramid fibers, ceramic fibers, and more stable friction coefficient (μ ≧ 0.38) has rapidly progressed. .
【0004】従来の技術では、上記の無機材料の研削剤
によって摩擦係数の安定化を図ってきたが、しかしなが
ら該研削剤は相手材の金属(ロータ)を攻撃し、その過
程でスキール音、異音等のノイズやジャダーが発生する
という欠点が生じる。ノイズやジャダーの発生を防止す
るには研削剤の使用を中止したり、使用量を低減すれば
よいが、このようにすると安定した摩擦係数を得ること
ができない。またSiO2、Al2O3、ZrO2、ZrS
iO3等の酸化物を含む研削材を用いると、ガラス状炭
素を構成している炭素が消失するという欠点が生じる。
現在の無機材料主体の研削剤以外のものを使用して、安
定した摩擦係数を有し、かつノイズやジャダーの発生を
完全に抑制した摩擦材が得られていないのが現状であ
る。In the prior art, the friction coefficient has been stabilized by the above-mentioned inorganic material abrasive. However, the abrasive attacks the metal (rotor) of the counterpart material, and in the process, squeal noise and abnormal noise are generated. There is a disadvantage that noise such as sound and judder are generated. In order to prevent the generation of noise and judder, the use of the abrasive may be stopped or the amount of the abrasive may be reduced, but in this case, a stable friction coefficient cannot be obtained. SiO 2 , Al 2 O 3 , ZrO 2 , ZrS
When an abrasive containing an oxide such as iO 3 is used, there is a disadvantage that carbon constituting glassy carbon disappears.
At present, a friction material having a stable friction coefficient and completely suppressing generation of noise and judder has not been obtained by using a material other than the current inorganic material-based abrasive.
【0005】[0005]
【発明が解決しようとする課題】請求項1記載の発明
は、安定した摩擦係数を有し、かつノイズやジャダーの
発生を抑えることができる摩擦材に適した摩擦材組成物
を提供するものである。請求項2記載の発明は、安定し
た摩擦係数を有し、かつノイズやジャダーの発生を抑え
ることが可能な摩擦材を提供するものである。SUMMARY OF THE INVENTION The present invention provides a friction material composition suitable for a friction material having a stable friction coefficient and capable of suppressing generation of noise and judder. is there. The invention described in claim 2 provides a friction material having a stable friction coefficient and capable of suppressing generation of noise and judder.
【0006】[0006]
【課題を解決するための手段】本発明は、全組成物中に
ガラス状炭素を0.3〜23重量%及び炭化珪素を0.
03〜12重量%含有してなる摩擦材組成物に関する。
また、本発明は、上記の摩擦材組成物を加熱加圧してな
る摩擦材に関する。According to the present invention, 0.3 to 23% by weight of glassy carbon and 0.1 to 0.2% by weight of silicon carbide are contained in the whole composition.
The present invention relates to a friction material composition containing from 03 to 12% by weight.
The present invention also relates to a friction material obtained by heating and pressurizing the above friction material composition.
【0007】[0007]
【発明の実施の形態】本発明において、ガラス状炭素の
含有量は全組成物中に0.3〜23重量%、好ましくは
0.5〜20重量%、より好ましくは5〜10重量%の
範囲とされ、0.3重量%未満であると研削剤としての
効果が十分に機能せず、安定した摩擦係数を得ることが
できない。一方23重量%を超えるとノイズやジャダー
の発生を抑えることができない。ガラス状炭素は、例え
ば液状の熱硬化性樹脂を硬化させた後、不活性雰囲気中
で炭化及び高温処理(黒鉛化処理)することにより得ら
れるが、本発明においては、熱硬化性樹脂を硬化させる
前に炭化珪素を均一に混合した後加熱処理を行なって硬
化させ、その後不活性雰囲気中で炭化及び高温処理(黒
鉛化処理)し、これを粉砕して使用される。DETAILED DESCRIPTION OF THE INVENTION In the present invention, the content of glassy carbon in the total composition is from 0.3 to 23% by weight, preferably from 0.5 to 20% by weight, more preferably from 5 to 10% by weight. When the content is less than 0.3% by weight, the effect as a grinding agent does not function sufficiently, and a stable friction coefficient cannot be obtained. On the other hand, if it exceeds 23% by weight, generation of noise and judder cannot be suppressed. Glassy carbon can be obtained by, for example, curing a liquid thermosetting resin, and then carbonizing and high-temperature treatment (graphitization treatment) in an inert atmosphere. In the present invention, the thermosetting resin is cured. Before the silicon carbide is uniformly mixed, heat treatment is performed and hardening is performed, and then carbonization and high temperature treatment (graphitization treatment) are performed in an inert atmosphere.
【0008】ガラス状炭素を得るための熱硬化性樹脂と
しては特に制限はないが、フラン樹脂、フェノール樹
脂、エポキシ樹脂、不飽和ポリエステル樹脂、メラミン
樹脂、アルキッド樹脂、キシレン樹脂等を挙げることが
できる。また、上記の樹脂の混合物を用いてもよい。本
発明においては上記の熱硬化性樹脂の他に必要に応じ、
トリクロロ酢酸、パラトルエンスルホン酸、硫酸等の硬
化剤が添加される。必要に応じ硬化剤が添加される場
合、熱硬化性樹脂と硬化剤の配合割合は、熱硬化性樹脂
100重量部に対して硬化剤が0.3〜10重量部の範
囲が好ましく、熱硬化性樹脂100重量部に対し硬化剤
が0.3〜7重量部の範囲であることがさらに好まし
い。The thermosetting resin for obtaining the glassy carbon is not particularly limited, and examples thereof include a furan resin, a phenol resin, an epoxy resin, an unsaturated polyester resin, a melamine resin, an alkyd resin, and a xylene resin. . Further, a mixture of the above resins may be used. In the present invention, if necessary in addition to the above thermosetting resin,
A curing agent such as trichloroacetic acid, paratoluenesulfonic acid, sulfuric acid and the like is added. When a curing agent is added as necessary, the mixing ratio of the thermosetting resin and the curing agent is preferably in the range of 0.3 to 10 parts by weight of the curing agent per 100 parts by weight of the thermosetting resin. More preferably, the curing agent is in the range of 0.3 to 7 parts by weight based on 100 parts by weight of the conductive resin.
【0009】また、炭化珪素は全組成物中0.03〜1
2重量%、好ましくは0.05〜10重量%、さらに好
ましくは0.05〜10重量%の範囲とされ、0.03
重量%未満であると安定した摩擦係数を得ることができ
ない。一方12重量%を超えるとノイズやジャダーの発
生を抑えることができない。Further, silicon carbide is contained in an amount of 0.03 to 1 in the total composition.
2% by weight, preferably 0.05 to 10% by weight, more preferably 0.05 to 10% by weight;
If it is less than% by weight, a stable friction coefficient cannot be obtained. On the other hand, if it exceeds 12% by weight, generation of noise and judder cannot be suppressed.
【0010】本発明における摩擦材組成物は、ガラス状
炭素及び炭化珪素の他に結合剤、補強繊維、潤滑剤、充
填剤等が用いられ、さらに必要に応じ黄銅、しんちゅう
等の金属粉が用いられる。本発明で用いられる結合剤
は、フェノール樹脂を用いることが好ましく、特にノボ
ラック樹脂、固形アンモニアレゾール樹脂、シリコン変
成フェノール樹脂、アクリル変成ゴムフェノール樹脂を
用いることが好ましい。本発明では上記結合剤に必要に
応じ硬化剤が添加される。結合剤は全組成物中に5〜2
0重量%含有することが好ましく、8〜14重量%含有
することがさらに好ましい。また必要に応じ添加される
硬化剤は、ヘキサメチレンテトラミン、パラホルムアル
デヒド、トリオキサン等が用いられ、結合剤中に8〜1
4重量%含有することが好ましく、10〜12重量%含
有することがさらに好ましい。In the friction material composition of the present invention, a binder, a reinforcing fiber, a lubricant, a filler and the like are used in addition to glassy carbon and silicon carbide. If necessary, a metal powder such as brass and brass is used. Used. The binder used in the present invention is preferably a phenol resin, and particularly preferably a novolak resin, a solid ammonia resol resin, a silicon-modified phenol resin, or an acrylic-modified rubber phenol resin. In the present invention, a curing agent is added to the binder as needed. The binder is present in the total composition at 5-2.
The content is preferably 0% by weight, more preferably 8 to 14% by weight. As a curing agent added as needed, hexamethylenetetramine, paraformaldehyde, trioxane, or the like is used.
The content is preferably 4% by weight, more preferably 10 to 12% by weight.
【0011】補強繊維としては、ガラス繊維、セラミッ
ク繊維、炭素繊維、鉱物繊維等の無機繊維、アラミド繊
維、ポリアミド繊維、ポリイミド繊維等の有機繊維、銅
繊維、黄銅繊維、スチール繊維等の金属繊維が用いられ
る。補強繊維は全組成物中に0.5〜16重量%含有す
ることが好ましく、3〜10重量%含有することがさら
に好ましい。Examples of the reinforcing fibers include inorganic fibers such as glass fibers, ceramic fibers, carbon fibers, and mineral fibers; organic fibers such as aramid fibers, polyamide fibers, and polyimide fibers; and metal fibers such as copper fibers, brass fibers, and steel fibers. Used. The reinforcing fiber is preferably contained in the entire composition in an amount of 0.5 to 16% by weight, more preferably 3 to 10% by weight.
【0012】また潤滑剤としては、黒鉛、硫化アンチモ
ン、硫化モリブデン等が、充填剤としては、カシューダ
スト、ゴムダスト、硫酸バリウム、炭酸カルシウム、炭
酸マグネシウム、シリカ、金属粉等が一種又は二種以上
混合して用いられる。潤滑剤は全組成物中に2〜8重量
%含有することが好ましく、3〜6重量%含有すること
がさらに好ましい。充填剤は全組成物中に10〜70重
量%含有することが好ましく、20〜60重量%含有す
ることがさらに好ましい。摩擦材組成物を構成する各成
分の使用割合は、それらの総量が100重量%になるよ
うに調整される。As a lubricant, graphite, antimony sulfide, molybdenum sulfide and the like are used. As a filler, cashew dust, rubber dust, barium sulfate, calcium carbonate, magnesium carbonate, silica, metal powder and the like are mixed. Used as The lubricant is preferably contained in the entire composition at 2 to 8% by weight, more preferably at 3 to 6% by weight. The filler is preferably contained in the entire composition in an amount of 10 to 70% by weight, more preferably 20 to 60% by weight. The usage ratio of each component constituting the friction material composition is adjusted so that the total amount thereof becomes 100% by weight.
【0013】本発明になる摩擦材は、金型内に裏金及び
摩擦材組成物を挿入及び充填した後、加熱加圧成形法で
一体成形するか又は加熱加圧成形後、接着剤を用いて裏
金と接着し、その後熱処理を行って得られる。なお摩擦
材を製造する際の加熱加圧条件及びそのあと工程の熱処
理条件については、特に制限はなく、従来公知の条件で
行うものとする。The friction material according to the present invention is obtained by inserting and filling a backing metal and a friction material composition into a mold, and then integrally molding by a heat and pressure molding method, or by using an adhesive after heating and pressure molding. It is obtained by bonding to the back metal and then performing heat treatment. The heating and pressurizing conditions for producing the friction material and the heat treatment conditions for the subsequent steps are not particularly limited, and are performed under conventionally known conditions.
【0014】[0014]
【実施例】以下本発明の実施例を説明するが、本発明は
これに制限するものではない。 実施例1〜7、比較例1〜6 黒鉛化処理後のガラス状炭素が表1及び表2になる量の
レゾール型フラン樹脂(日立化成工業(株)製、商品名V
P−13N)と炭化珪素を表1及び表2に示す量配合
し、均一に混合した後保温器に入れ、10℃/時間の昇
温速度で160℃まで昇温し、160℃で5時間保持し
て硬化処理を行い炭化珪素含有樹脂板を得た。EXAMPLES Examples of the present invention will be described below, but the present invention is not limited thereto. Examples 1 to 7 and Comparative Examples 1 to 6 Resor-type furan resins (manufactured by Hitachi Chemical Co., Ltd., trade name V
P-13N) and silicon carbide were blended in the amounts shown in Tables 1 and 2 and mixed uniformly, then placed in a warmer, heated to 160 ° C at a rate of 10 ° C / hour, and heated at 160 ° C for 5 hours. The resin was held and subjected to a curing treatment to obtain a silicon carbide-containing resin plate.
【0015】次に炭化珪素含有樹脂板を、窒素ガス雰囲
気中で1000℃で30日保持して炭化焼成し、その後
2000℃まで昇温させ、2000℃で10時間保持し
て黒鉛化処理を行い、炭化珪素含有ガラス状炭素を得
た。得られた炭化珪素含有ガラス状炭素は、厚みが2.
0〜3.5mmの範囲で、密度が1.56g/cm3、電気比
抵抗が10000μΩ−cm及び20〜400℃の熱膨張
係数が2.2×10-6deg-1であった。Next, the silicon carbide-containing resin plate is carbonized and fired at 1000 ° C. for 30 days in a nitrogen gas atmosphere, then heated to 2000 ° C., and held at 2000 ° C. for 10 hours for graphitization. Thus, silicon carbide-containing glassy carbon was obtained. The obtained silicon carbide-containing glassy carbon has a thickness of 2.
Within the range of 0 to 3.5 mm, the density was 1.56 g / cm 3 , the electrical resistivity was 10,000 μΩ-cm, and the coefficient of thermal expansion at 20 to 400 ° C. was 2.2 × 10 −6 deg −1 .
【0016】上記で得た炭化珪素含有ガラス状炭素を粉
砕して平均粒径が7μmの炭化珪素含有ガラス状炭素粉
を得た。次いでこの炭化珪素含有ガラス状炭素粉と表1
及び表2に示す成分を配合し、混合機で均一に混合して
摩擦材組成物を得た。この後、140℃、圧力400MP
aの条件で12分間加熱加圧成形し、さらに200℃で
5時間熱処理を行ってディスクブレーキパッドを得た。The silicon carbide-containing glassy carbon obtained above was pulverized to obtain silicon carbide-containing glassy carbon powder having an average particle diameter of 7 μm. Next, this silicon carbide-containing glassy carbon powder and
And the components shown in Table 2 were blended and uniformly mixed with a mixer to obtain a friction material composition. After this, 140 ° C, pressure 400MP
Heat-press molding was performed under the condition of a for 12 minutes, and heat treatment was further performed at 200 ° C. for 5 hours to obtain a disc brake pad.
【0017】[0017]
【表1】 [Table 1]
【0018】[0018]
【表2】 [Table 2]
【0019】次に本発明になるディスクブレーキパッド
と比較例のディスクブレーキパッドとについて、比較試
験を行った。その試験結果を表3及び表4に示す。なお
試験条件は下記の通りである。 剪断強度 JASO、C427に従い、22℃及び300℃におけ
る強度を測定した。 耐摩耗性 キャリパ型式:コレットタイプ(シリンダ面積28.8
cm2) 試験条件:JASO、C427に従い、イナーシャ…4
9kgm2、制動初速度…60km/時間、減速度…2.94
m/秒2、制動前温度…250℃、制動回数…各100
0回毎の条件で摩耗量を測定した。Next, a comparative test was performed on the disc brake pad according to the present invention and the disc brake pad of the comparative example. The test results are shown in Tables 3 and 4. The test conditions are as follows. Shear strength The strength at 22 ° C and 300 ° C was measured according to JASO, C427. Wear resistance Caliper model: Collet type (cylinder area 28.8
cm 2 ) Test conditions: Inertia according to JASO, C427 ... 4
9kgm 2 , initial braking speed: 60km / h, deceleration: 2.94
m / sec. 2, braking before temperature ... 250 ℃, braking number of times ... each 100
The wear amount was measured under the condition of every 0 times.
【0020】 異音の発生状況及び効力 2000ccのオートマチック車(日産自動車(株)製、車
種名セドリック(Y32))でJASO、C402の実車
試験を行い、試験中の異音を測定し、70dB以上の異音
の発生率及び最大音圧を求めた。また効力については、
試験中のディスクブレーキとしての効力をμ値で、相手
材表面攻撃量をロータの研削量で評価した。 成形性 ディスクブレーキパッドの外観を目視し、皺及び亀裂の
発生の有無について観察した。[0020] Abnormal noise generation situation and effectiveness JASO, C402 actual vehicle test was performed on a 2000cc automatic car (Nissan Motor Co., Ltd., model name Cedric (Y32)), and the abnormal noise during the test was measured, and 70dB or more. The occurrence rate of abnormal noise and the maximum sound pressure were determined. Regarding efficacy,
The effectiveness as a disc brake during the test was evaluated by the μ value, and the amount of attack on the surface of the partner material was evaluated by the amount of grinding of the rotor. Formability The appearance of the disc brake pad was visually observed, and the occurrence of wrinkles and cracks was observed.
【0021】[0021]
【表3】 [Table 3]
【0022】[0022]
【表4】 [Table 4]
【0023】表3に示されるように、本発明になるディ
スクブレーキパッドは、皺及び亀裂の発生がなく、全て
の特性に優れることが確認された。これに対し表4に示
されるように、比較例のディスクブレーキパッドは、い
ずれかの特性に欠点が生じ、良好な結果が得られなかっ
た。As shown in Table 3, it was confirmed that the disc brake pad according to the present invention was free from wrinkles and cracks and was excellent in all properties. On the other hand, as shown in Table 4, in the disc brake pad of the comparative example, a defect occurred in any of the characteristics, and good results were not obtained.
【0024】[0024]
【発明の効果】請求項1における摩擦材組成物は、安定
した摩擦係数(μ≧0.38)を有し、かつノイズ発生
やジャダー発生を抑えることができる摩擦材を提供する
ことができる。請求項2における摩擦材は、安定した摩
擦係数(μ≧0.38)を有し、かつノイズ発生やジャ
ダー発生を抑えることが可能で、工業的に極めて好適で
ある。The friction material composition according to the first aspect can provide a friction material having a stable friction coefficient (μ ≧ 0.38) and capable of suppressing generation of noise and judder. The friction material according to claim 2 has a stable friction coefficient (μ ≧ 0.38) and can suppress generation of noise and judder, and is industrially extremely suitable.
Claims (2)
3重量%及び炭化珪素を0.03〜12重量%含有して
なる摩擦材組成物。1. A glassy carbon in a total composition of 0.3 to 2%.
A friction material composition containing 3% by weight and 0.03 to 12% by weight of silicon carbide.
成形してなる摩擦材。2. A friction material formed by heating and pressing the friction material composition according to claim 1.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14635897A JPH10330732A (en) | 1997-06-04 | 1997-06-04 | Friction material composition and friction material made therefrom |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14635897A JPH10330732A (en) | 1997-06-04 | 1997-06-04 | Friction material composition and friction material made therefrom |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH10330732A true JPH10330732A (en) | 1998-12-15 |
Family
ID=15405919
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP14635897A Pending JPH10330732A (en) | 1997-06-04 | 1997-06-04 | Friction material composition and friction material made therefrom |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH10330732A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1126003A1 (en) * | 2000-02-16 | 2001-08-22 | Mitsubishi Materials Corporation | Resin bonded abrasive tool |
| US6383238B1 (en) * | 1999-08-17 | 2002-05-07 | Mitsubishi Materials Corporation | Resin bonded abrasive tool |
| KR100576970B1 (en) | 2004-11-30 | 2006-05-10 | 한국타이어 주식회사 | Steel-based friction material composition for race cars |
| US7166523B2 (en) * | 2000-08-10 | 2007-01-23 | Hoya Corporation | Silicon carbide and method of manufacturing the same |
| CN101839294A (en) * | 2010-05-20 | 2010-09-22 | 湖南博云汽车制动材料有限公司 | Nonmetal ceramic matrix drum brake pad for bus and preparation method thereof |
| CN104235242A (en) * | 2014-08-28 | 2014-12-24 | 万山特区宏安摩擦材料有限公司 | Carbon-based ceramic brake block and preparing method of carbon-based ceramic brake block |
| CN105134843A (en) * | 2015-08-26 | 2015-12-09 | 万山特区宏安摩擦材料有限公司 | Ceramic friction material and raw material mixing method thereof |
-
1997
- 1997-06-04 JP JP14635897A patent/JPH10330732A/en active Pending
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6383238B1 (en) * | 1999-08-17 | 2002-05-07 | Mitsubishi Materials Corporation | Resin bonded abrasive tool |
| KR100615896B1 (en) * | 1999-08-17 | 2006-08-28 | 미츠비시 마테리알 가부시키가이샤 | Resin bonded abresive tool |
| EP1126003A1 (en) * | 2000-02-16 | 2001-08-22 | Mitsubishi Materials Corporation | Resin bonded abrasive tool |
| US7166523B2 (en) * | 2000-08-10 | 2007-01-23 | Hoya Corporation | Silicon carbide and method of manufacturing the same |
| KR100576970B1 (en) | 2004-11-30 | 2006-05-10 | 한국타이어 주식회사 | Steel-based friction material composition for race cars |
| CN101839294A (en) * | 2010-05-20 | 2010-09-22 | 湖南博云汽车制动材料有限公司 | Nonmetal ceramic matrix drum brake pad for bus and preparation method thereof |
| CN101839294B (en) | 2010-05-20 | 2013-01-09 | 湖南博云汽车制动材料有限公司 | Nonmetal ceramic matrix drum brake pad for bus and preparation method thereof |
| CN104235242A (en) * | 2014-08-28 | 2014-12-24 | 万山特区宏安摩擦材料有限公司 | Carbon-based ceramic brake block and preparing method of carbon-based ceramic brake block |
| CN105134843A (en) * | 2015-08-26 | 2015-12-09 | 万山特区宏安摩擦材料有限公司 | Ceramic friction material and raw material mixing method thereof |
| CN105134843B (en) * | 2015-08-26 | 2017-08-25 | 贵州宏安制动器科技有限公司 | A kind of ceramic frication material and its method for mixing raw materials |
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