JP2002309234A - Friction material composition, manufacturing method of the same and friction material using the same - Google Patents
Friction material composition, manufacturing method of the same and friction material using the sameInfo
- Publication number
- JP2002309234A JP2002309234A JP2001114365A JP2001114365A JP2002309234A JP 2002309234 A JP2002309234 A JP 2002309234A JP 2001114365 A JP2001114365 A JP 2001114365A JP 2001114365 A JP2001114365 A JP 2001114365A JP 2002309234 A JP2002309234 A JP 2002309234A
- Authority
- JP
- Japan
- Prior art keywords
- friction material
- material composition
- friction
- weight
- fiber
- 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 62
- 239000000203 mixture Substances 0.000 title claims abstract description 53
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 8
- 239000000835 fiber Substances 0.000 claims abstract description 72
- 229910052751 metal Inorganic materials 0.000 claims abstract description 51
- 239000002184 metal Substances 0.000 claims abstract description 51
- 229920001971 elastomer Polymers 0.000 claims abstract description 28
- 239000000463 material Substances 0.000 claims abstract description 28
- 239000000806 elastomer Substances 0.000 claims abstract description 18
- 229920005549 butyl rubber Polymers 0.000 claims abstract description 13
- 239000011230 binding agent Substances 0.000 claims abstract description 9
- 229920002379 silicone rubber Polymers 0.000 claims abstract description 8
- 239000004945 silicone rubber Substances 0.000 claims abstract description 7
- 239000000126 substance Substances 0.000 claims abstract description 7
- 238000010438 heat treatment Methods 0.000 claims abstract description 6
- 229920001973 fluoroelastomer Polymers 0.000 claims abstract description 4
- 238000002156 mixing Methods 0.000 claims abstract description 3
- 238000000034 method Methods 0.000 claims description 10
- 239000005060 rubber Substances 0.000 claims description 10
- 239000003607 modifier Substances 0.000 claims description 9
- 239000011248 coating agent Substances 0.000 claims description 4
- 238000000576 coating method Methods 0.000 claims description 4
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 3
- 239000011737 fluorine Substances 0.000 claims description 3
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- 238000003825 pressing Methods 0.000 claims description 2
- 230000006866 deterioration Effects 0.000 abstract description 7
- 230000003647 oxidation Effects 0.000 abstract description 5
- 238000007254 oxidation reaction Methods 0.000 abstract description 5
- 238000000465 moulding Methods 0.000 abstract description 3
- 238000005204 segregation Methods 0.000 abstract description 3
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- 239000007788 liquid Substances 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 9
- 229910001369 Brass Inorganic materials 0.000 description 7
- 239000010951 brass Substances 0.000 description 7
- 229910000831 Steel Inorganic materials 0.000 description 6
- 239000010959 steel Substances 0.000 description 6
- 230000001590 oxidative effect Effects 0.000 description 5
- 244000226021 Anacardium occidentale Species 0.000 description 4
- 229920000459 Nitrile rubber Polymers 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 238000005299 abrasion Methods 0.000 description 4
- 235000020226 cashew nut Nutrition 0.000 description 4
- 230000013011 mating Effects 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000003981 vehicle Substances 0.000 description 3
- 229920002972 Acrylic fiber Polymers 0.000 description 2
- 229910000906 Bronze Inorganic materials 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 229920000049 Carbon (fiber) Polymers 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 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
- 239000010974 bronze Substances 0.000 description 2
- 239000004917 carbon fiber Substances 0.000 description 2
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 description 2
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 239000002657 fibrous material Substances 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 235000021388 linseed oil Nutrition 0.000 description 2
- 239000000944 linseed oil Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000011490 mineral wool Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000002436 steel type Substances 0.000 description 2
- YLZOPXRUQYQQID-UHFFFAOYSA-N 3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]propan-1-one Chemical group N1N=NC=2CN(CCC=21)CCC(=O)N1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F YLZOPXRUQYQQID-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004944 Liquid Silicone Rubber Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- MKYBYDHXWVHEJW-UHFFFAOYSA-N N-[1-oxo-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propan-2-yl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical group O=C(C(C)NC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 MKYBYDHXWVHEJW-UHFFFAOYSA-N 0.000 description 1
- 101100121112 Oryza sativa subsp. indica 20ox2 gene Proteins 0.000 description 1
- 101100121113 Oryza sativa subsp. japonica GA20OX2 gene Proteins 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229940007424 antimony trisulfide Drugs 0.000 description 1
- NVWBARWTDVQPJD-UHFFFAOYSA-N antimony(3+);trisulfide Chemical compound [S-2].[S-2].[S-2].[Sb+3].[Sb+3] NVWBARWTDVQPJD-UHFFFAOYSA-N 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- 239000011344 liquid material 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
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000011812 mixed powder Substances 0.000 description 1
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 1
- 229910052982 molybdenum disulfide Inorganic materials 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- -1 polyethylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000012783 reinforcing fiber Substances 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 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、各種産業用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、摩擦材組成物の製造法及び摩擦材組成物を
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 production of the friction material composition. And a friction material using the friction material composition.
【0002】[0002]
【従来の技術】自動車、鉄道車両、各種産業用機械等に
は、その制動のため摩擦材が使用されている。この摩擦
材としては、現在非アスベスト系ディスクブレーキパッ
ドが主流であり、特公昭59−4462号公報、特開平
6−184525号公報に示されるように補強繊維とし
て、スチール繊維、黄銅繊維、銅繊維等の金属繊維、ア
クリル繊維、アラミド繊維、フェノール繊維等の有機質
繊維、ロックウール、チタン酸カリウム繊維、アルミナ
シリカ繊維、カーボン繊維等の無機質繊維を組み合わせ
たものが使用されている。2. Description of the Related Art Friction materials are used in automobiles, railway vehicles, various industrial machines and the like for braking. As the friction material, non-asbestos disc brake pads are currently the mainstream, and as shown in JP-B-59-4462 and JP-A-6-184525, steel fibers, brass fibers, and copper fibers are used as reinforcing fibers. A combination of organic fibers such as metal fibers such as acrylic fibers, aramid fibers, and phenol fibers, and inorganic fibers such as rock wool, potassium titanate fiber, alumina silica fiber, and carbon fiber is used.
【0003】しかしながら、従来の非アスベスト系ディ
スクブレーキパッドなどの摩擦材を構成する材料を乾式
で混合する場合、材料の脱落、特に金属繊維の脱落が発
生する問題があった。金属繊維は、摩擦材に使用する他
の材料に比較して比重と繊維径が大きいため、脱落を起
こし易く不均一分散となる。金属繊維が脱落すると摩擦
材の摩擦性能、摩耗性能及び物性が不均一になり、また
金属繊維の不均一分散により亀裂が発生する場合があ
る。さらに金属繊維を多く含有する摩擦材は、金属繊維
の酸化により摩擦性能が変化し、鳴き、異音等の音振性
能が悪化する場合があった。[0003] However, when a material constituting a friction material such as a conventional non-asbestos-type disc brake pad is dry-mixed, there is a problem that the material is dropped, particularly the metal fibers are dropped. Metal fibers have a large specific gravity and a large fiber diameter as compared with other materials used for the friction material, and thus are liable to fall off and become non-uniformly dispersed. When the metal fibers fall off, the friction performance, wear performance and physical properties of the friction material become non-uniform, and cracks may occur due to non-uniform dispersion of the metal fibers. Further, in a friction material containing a large amount of metal fibers, the friction performance may be changed due to oxidation of the metal fibers, and the sound and vibration performance such as squealing and abnormal noise may be deteriorated.
【0004】上記の問題点の対応策として、金属繊維に
対してカシューナット殻油又はアマニ油を被覆し、材料
の脱落を防止する方法がある。しかし上記の方法では、
カシューナット殻油又はアマニ油の粘着力が不十分であ
るため、金属繊維の分散性が不十分であったり、有機溶
剤を除去するための乾燥工程が必要であり、混合粉を製
作するのに工程が複雑になるなどの欠点があった。As a countermeasure against the above problem, there is a method of coating metal fibers with cashew nut shell oil or linseed oil to prevent the material from falling off. But with the above method,
Due to insufficient adhesive force of cashew nut shell oil or linseed oil, dispersibility of metal fibers is insufficient, and a drying process to remove organic solvent is necessary, and it is necessary to manufacture mixed powder. There were drawbacks such as a complicated process.
【0005】[0005]
【発明が解決しようとする課題】請求項1及び2記載の
発明は、金属繊維の脱落と偏析の発生が少なく、金属繊
維の酸化劣化を抑え、音振性能、効き及び耐摩耗性に優
れた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3記載の発明は、金属繊維の脱落と偏析が少
なく、金属繊維の酸化劣化を抑え、音振性能、効き及び
耐摩耗性に優れた摩擦材に適した摩擦材組成物の製造法
を提供するものである。請求項4記載の発明は、金属繊
維の酸化劣化を抑え、音振性能、効き及び耐摩耗性に優
れた摩擦材を提供するものである。According to the first and second aspects of the invention, the metal fibers are less likely to fall off and segregate, the oxidation deterioration of the metal fibers is suppressed, and the sound vibration performance, effectiveness and wear resistance are excellent. An object of the present invention is to provide a friction material composition suitable for a friction material. The invention according to claim 3 provides a method for producing a friction material composition suitable for a friction material having little metal fiber falling off and segregation, suppressing oxidative deterioration of the metal fiber, and having excellent sound vibration performance, effectiveness and abrasion resistance. To provide. The fourth aspect of the present invention is to provide a friction material which suppresses oxidative deterioration of metal fibers and has excellent sound vibration performance, effectiveness and wear resistance.
【0006】[0006]
【課題を解決するための手段】本発明は、繊維状物質、
結合剤及び摩擦調整剤を含む摩擦材組成物において、表
面がブチルゴム、シリコーンゴム、フッ素ゴムのうち1
種類以上のエラストマーで被覆された金属繊維を10〜
50重量%含有してなる摩擦材組成物に関する。また、
本発明は、エラストマーが金属繊維100重量部に対し
て2〜15重量部である摩擦材組成物に関する。また、
本発明は、金属繊維をブチルゴム、シリコーンゴム、フ
ッ素ゴムのうち1種類以上のエラストマーで被覆した
後、他の繊維状物質、結合剤及び摩擦調整剤を含む材料
を添加し、混合することを特徴とする摩擦材組成物の製
造法に関する。さらに、本発明は、上記の摩擦材組成物
又は上記の方法で製造された摩擦材組成物を加熱加圧成
形してなる摩擦材に関する。The present invention provides a fibrous material,
In a friction material composition containing a binder and a friction modifier, the surface has one of butyl rubber, silicone rubber and fluoro rubber.
Metal fibers coated with more than one type of elastomer
The present invention relates to a friction material composition containing 50% by weight. Also,
The present invention relates to a friction material composition in which an elastomer is 2 to 15 parts by weight based on 100 parts by weight of a metal fiber. Also,
The present invention is characterized in that a metal fiber is coated with at least one kind of elastomer among butyl rubber, silicone rubber and fluorine rubber, and then a material containing another fibrous substance, a binder and a friction modifier is added and mixed. And a method for producing a friction material composition. Furthermore, the present invention relates to a friction material obtained by subjecting the above-mentioned friction material composition or the friction material composition produced by the above-mentioned method to heat and pressure molding.
【0007】[0007]
【発明の実施の形態】本発明において、金属繊維を被覆
するエラストマーは、分散性、気密性、耐酸化性等の面
からブチルゴム(IIR系ゴム)、シリコーンゴム(S
i系ゴム)、フッ素ゴム(FR系ゴム)の液状物を用い
ることが適当であり、少なくとも1種類以上のエラスト
マーで被覆することが好ましい。これらのエラストマー
は、有機溶剤を使用せず、必要に応じて硫黄や硬化促進
剤を配合して用いることが好ましい。BEST MODE FOR CARRYING OUT THE INVENTION In the present invention, the elastomer covering metal fibers is made of butyl rubber (IIR rubber) or silicone rubber (S) in terms of dispersibility, airtightness and oxidation resistance.
It is appropriate to use a liquid material of i-type rubber) and fluorine rubber (FR-type rubber), and it is preferable to coat with at least one kind of elastomer. It is preferable that these elastomers are used without using an organic solvent and, if necessary, are compounded with sulfur or a curing accelerator.
【0008】被覆するエラストマーの量は、金属繊維1
00重量部に対して2〜15重量部の範囲が好ましく、
4〜13重量部の範囲がより好ましく、6〜12重量部
の範囲がさらに好ましい。2重量部未満であると分散
性、気密性及び耐酸化性が低下すると共にブレーキ鳴き
が悪化する傾向があり、15重量部を超えると耐フェー
ド性が悪化する傾向がある。[0008] The amount of the elastomer to be coated is
The range of 2 to 15 parts by weight relative to 00 parts by weight is preferable,
The range is more preferably from 4 to 13 parts by weight, and even more preferably from 6 to 12 parts by weight. If the amount is less than 2 parts by weight, dispersibility, airtightness and oxidation resistance tend to decrease, and brake squeal tends to deteriorate. If the amount exceeds 15 parts by weight, fade resistance tends to deteriorate.
【0009】また、表面がエラストマーで被覆された金
属繊維は、全組成物中に10〜50重量%、好ましくは
15〜45重量%、さらに好ましくは20〜40重量%
の範囲とされ、10重量%未満であると効きと耐摩耗性
が低下し、50重量%を超えるとブレーキ鳴きや相手材
攻撃性が大きくなる。本発明に用いられる金属繊維とし
ては、例えばスチール繊維、黄銅繊維、銅繊維、りん青
銅繊維等が挙げられ、このうちスチール繊維及び黄銅繊
維を用いることが好ましい。Further, the metal fiber whose surface is coated with the elastomer is 10 to 50% by weight, preferably 15 to 45% by weight, more preferably 20 to 40% by weight in the total composition.
If it is less than 10% by weight, the effectiveness and abrasion resistance are reduced, and if it is more than 50% by weight, brake squeal and aggressiveness of a mating material are increased. Examples of the metal fiber used in the present invention include steel fiber, brass fiber, copper fiber, phosphor bronze fiber and the like, and among them, steel fiber and brass fiber are preferably used.
【0010】なお、金属繊維にエラストマーを被覆する
手法は、均一に被覆するためニーダで加圧混練すること
が好ましい。エラストマーの粘度は、金属繊維への被覆
し易さの点で5〜1000Pa.sの範囲であることが
好ましく、20〜500Pa.sの範囲であることがさ
らに好ましい。It is preferable that the metal fiber is coated with the elastomer by pressure kneading with a kneader in order to uniformly coat the metal fiber. The viscosity of the elastomer is 5 to 1000 Pa.s in terms of ease of coating on the metal fiber. s, and preferably 20 to 500 Pa.s. More preferably, it is in the range of s.
【0011】本発明における摩擦材部の材質は、セミメ
タリック系、ロースチール系、ノンスチール系のいずれ
にも適用でき特に制限はない。また、摩擦材に用いられ
る材料は、上記の金属繊維及びエラストマーの他、一般
に公知の材料が用いられ、例えば、アラミド繊維、アク
リル繊維、フェノール繊維、セラミック繊維、ロックウ
ール、チタン酸カリウム繊維、カーボン繊維等の繊維状
物質、フェノール樹脂、エポキシ樹脂、メラミン樹脂、
カシュー樹脂等の熱硬化性樹脂やNBR、SBR、IR
等のゴム組成物を含む結合剤、カシューダスト、ゴムダ
スト等の有機質摩擦調整剤、硫酸バリウム、黒鉛、コー
クス、三硫化アンチモン、二硫化モリブデン、マイカ、
ジルコニア、シリカ、アルミナ、炭酸カルシウム、炭酸
マグネシウム等の無機質摩擦調整剤などが用いられ、さ
らに必要に応じて黄銅、りん青銅、銅、亜鉛等の金属粉
が添加される。The material of the friction material portion in the present invention can be applied to any of a semi-metallic type, a low steel type, and a non-steel type, and is not particularly limited. In addition, the material used for the friction material is, in addition to the above metal fibers and elastomers, generally known materials, for example, aramid fiber, acrylic fiber, phenol fiber, ceramic fiber, rock wool, potassium titanate fiber, carbon fiber Fibrous substances such as fibers, phenolic resins, epoxy resins, melamine resins,
Thermosetting resin such as cashew resin, NBR, SBR, IR
Binders containing rubber compositions such as, cashew dust, organic friction modifiers such as rubber dust, barium sulfate, graphite, coke, antimony trisulfide, molybdenum disulfide, mica,
Inorganic friction modifiers such as zirconia, silica, alumina, calcium carbonate, and magnesium carbonate are used, and metal powders such as brass, phosphor bronze, copper, and zinc are added as necessary.
【0012】上記におけるエラストマーで被覆された金
属繊維を含む繊維状物質の含有量は全組成物中に10〜
60重量%とすることが好ましく、15〜55重量%と
することがさらに好ましい。結合剤の含有量は、全組成
物中に5〜20重量%とすることが好ましく、10〜1
5重量%とすることがさらに好ましい。有機摩擦調整剤
の含有量は、全組成物中に3〜20重量%とすることが
好ましく、6〜15重量%とすることがさらに好まし
い。また無機質摩擦調整剤の含有量は、全組成物中に2
0〜50重量%とすることが好ましく、25〜45重量
%とすることがさらに好ましい。The content of the fibrous material including the metal fibers coated with the elastomer in the above is 10 to 10 in the total composition.
It is preferably 60% by weight, more preferably 15 to 55% by weight. The content of the binder is preferably 5 to 20% by weight in the whole composition, and 10 to 1% by weight.
More preferably, the content is 5% by weight. The content of the organic friction modifier is preferably from 3 to 20% by weight, more preferably from 6 to 15% by weight in the whole composition. The content of the inorganic friction modifier is 2% in the total composition.
The content is preferably 0 to 50% by weight, more preferably 25 to 45% by weight.
【0013】なお、必要に応じて添加する金属粉の含有
量は、全組成物中に5〜30重量%とすることが好まし
く、10〜25重量%とすることがさらに好ましい。こ
れらの成分は、全組成物が100重量%となるように配
合される。The content of the metal powder added as necessary is preferably 5 to 30% by weight, more preferably 10 to 25% by weight, based on the whole composition. These components are blended so that the total composition becomes 100% by weight.
【0014】本発明になる摩擦材は、金属繊維をエラス
トマーで被覆した後、他の繊維状物質、結合剤及び有機
・無機の摩擦調整剤を含む材料を添加して均一に混合
し、この混合物を予備成形し、次いで金型内に裏金及び
予備成形体を挿設した後、加熱加圧成形法で成形し、そ
の後熱処理を行い、必要に応じて表面の有機成分を除去
するためスコーチ処理を行って得られる。The friction material according to the present invention is obtained by coating a metal fiber with an elastomer, adding a material containing another fibrous substance, a binder, and an organic / inorganic friction modifier, and uniformly mixing the mixture. Pre-molded, then insert the backing metal and the pre-molded body into the mold, mold by the heat and pressure molding method, then perform heat treatment, and if necessary, perform scorch treatment to remove organic components on the surface Obtained by going.
【0015】なお材料を混合する場合、乾式法で混合す
ることが好ましく、また成形する際の加熱温度は130
〜180℃が好ましく、140〜170℃がより好まし
い。圧力は20〜60MPaが好ましく、30〜50M
Paがより好ましい。熱処理温度は180〜250℃が
好ましく、200〜230℃がより好ましい。必要に応
じて行うスコーチ処理は、摩擦部材に熱盤を押し当てる
方法、ガスの炎などの直火で加熱する方法等があり特に
制限はない。またスコーチ処理の条件については、その
材質に合った条件を選定して処理すればよい。When the materials are mixed, it is preferable to mix them by a dry method.
-180 ° C is preferred, and 140-170 ° C is more preferred. The pressure is preferably 20 to 60 MPa, and 30 to 50 M
Pa is more preferred. The heat treatment temperature is preferably from 180 to 250C, more preferably from 200 to 230C. The scorch treatment performed as necessary includes a method of pressing a hot plate against a friction member, a method of heating with a direct fire such as a gas flame, and the like, and is not particularly limited. Further, as for the conditions of the scorch processing, the processing may be performed by selecting conditions suitable for the material.
【0016】[0016]
【実施例】以下本発明を実施例により説明する。 実施例1 金属繊維(スチール繊維及び黄銅繊維)100重量部に
対して粘度が70Pa・sの液状ブチルゴム(以下液状
IIRとする)4重量部と粘度が70Pa・sの液状ニ
トリルブタジエンゴム(以下液状NBRとする)4重量
部をニーダで49MPaの圧力で5分間混練して金属繊
維を液状IIRと液状NBRで被覆し、表1に示すA材
を得た。次いで、表2に示す他の成分を表2に示す量秤
量し、混合機で3000r/minの回転速度で4分間
混合し、摩擦材組成物を得た。The present invention will be described below with reference to examples. Example 1 4 parts by weight of liquid butyl rubber (hereinafter referred to as liquid IIR) having a viscosity of 70 Pa · s and liquid nitrile butadiene rubber (hereinafter referred to as liquid) having a viscosity of 70 Pa · s based on 100 parts by weight of metal fiber (steel fiber and brass fiber) 4 parts by weight (referred to as NBR) were kneaded with a kneader at a pressure of 49 MPa for 5 minutes, and the metal fibers were coated with liquid IIR and liquid NBR to obtain a material A shown in Table 1. Next, the other components shown in Table 2 were weighed and mixed in a mixer at a rotation speed of 3000 r / min for 4 minutes to obtain a friction material composition.
【0017】実施例2 金属繊維(スチール繊維及び黄銅繊維)100重量部に
対して粘度が70Pa・sの液状シリコーンゴム(以下
液状Siゴムとする)2重量部をニーダで49MPaの
圧力で5分間混練して金属繊維を液状Siゴムで被覆
し、表1に示すB材を得た。次いで表2に示す他の成分
を表2に示す量秤量し、混合機で3000r/minの
回転速度で4分間混合し、摩擦材組成物を得た。Example 2 2 parts by weight of a liquid silicone rubber (hereinafter referred to as liquid Si rubber) having a viscosity of 70 Pa · s with respect to 100 parts by weight of a metal fiber (steel fiber and brass fiber) are kneaded with a kneader at a pressure of 49 MPa for 5 minutes. After kneading, the metal fibers were coated with liquid Si rubber to obtain material B shown in Table 1. Next, the other components shown in Table 2 were weighed and mixed in a mixer at a rotation speed of 3000 r / min for 4 minutes to obtain a friction material composition.
【0018】実施例3 金属繊維(スチール繊維及び黄銅繊維)100重量部に
対して粘度が70Pa・sの液状IIR15重量部をニ
ーダで49MPaの圧力で5分間混練して金属繊維を液
状IIRで被覆し、表1に示すC材を得た。次いで表2
に示す他の成分を表2に示す量秤量し、混合機で300
0r/minの回転速度で4分間混合し、摩擦材組成物
を得た。Example 3 15 parts by weight of a liquid IIR having a viscosity of 70 Pa · s with respect to 100 parts by weight of a metal fiber (steel fiber and brass fiber) are kneaded with a kneader at a pressure of 49 MPa for 5 minutes to coat the metal fiber with a liquid IIR. Then, a C material shown in Table 1 was obtained. Then Table 2
The other components shown in Table 2 were weighed in the amounts shown in Table 2, and mixed with a mixer.
The mixture was mixed at a rotation speed of 0 r / min for 4 minutes to obtain a friction material composition.
【0019】実施例4 実施例1で得たA材を用いて、表2に示す他の成分を表
2に示す量秤量し、混合機で3000r/minの回転
速度で4分間混合し、摩擦材組成物を得た。Example 4 Using the material A obtained in Example 1, the other components shown in Table 2 were weighed and mixed in a mixer at a rotation speed of 3000 r / min for 4 minutes to obtain a friction material. A material composition was obtained.
【0020】実施例5 実施例1で得たA材を用いて、表2に示す他の成分を表
2に示す量秤量し、混合機で3000r/minの回転
速度で4分間混合し、摩擦材組成物を得た。Example 5 Using the material A obtained in Example 1, other components shown in Table 2 were weighed and mixed in a mixer at a rotation speed of 3000 r / min for 4 minutes. A material composition was obtained.
【0021】比較例1 実施例1で得たA材を用いて、表2に示す他の成分を表
2に示す量秤量し、混合機で3000r/minの回転
速度で4分間混合し、摩擦材組成物を得た。COMPARATIVE EXAMPLE 1 Using the material A obtained in Example 1, other components shown in Table 2 were weighed and mixed in a mixer at a rotation speed of 3000 r / min for 4 minutes. A material composition was obtained.
【0022】比較例2 実施例1で得たA材を用いて、表2に示す他の成分を表
2に示す量秤量し、混合機で3000r/minの回転
速度で4分間混合し、摩擦材組成物を得た。Comparative Example 2 Using the material A obtained in Example 1, the other components shown in Table 2 were weighed and mixed in a mixer at a rotation speed of 3000 r / min for 4 minutes to obtain a friction material. A material composition was obtained.
【0023】次に実施例1〜5及び比較例1〜2で得ら
れた摩擦材組成物を各々予備成形し、次いで金型内にデ
ィスクブレーキパッドの裏金及び予備成形体を挿設し、
その後150±5℃及び圧力49MPaの条件で5分間
加熱加圧成形した。さらに200℃で5時間熱処理行
い、冷却後研磨し、470±10℃で5分間の表面スコ
ーチ処理を行ってディスクブレーキパッドを得た。Next, the friction material compositions obtained in Examples 1 to 5 and Comparative Examples 1 and 2 were each preformed, and then the backing of the disc brake pad and the preformed body were inserted into a mold.
Thereafter, it was heated and pressed at 150 ± 5 ° C. and 49 MPa for 5 minutes. Further, heat treatment was performed at 200 ° C. for 5 hours, and after cooling, polishing and surface scorch treatment were performed at 470 ± 10 ° C. for 5 minutes to obtain a disc brake pad.
【0024】[0024]
【表1】 [Table 1]
【0025】[0025]
【表2】 [Table 2]
【0026】次に、上記で得た本発明になる実施例1〜
5の摩擦組成物とディスクブレーキパッド及び比較例1
〜2の摩擦材組成物とディスクブレーキパッドについて
比較試験を行った。その試験結果を表3に示す。なお試
験条件は下記の通りである。Next, Examples 1 to 4 according to the present invention obtained above will be described.
Composition and Disc Brake Pad of Comparative Example 5 and Comparative Example 1
Comparative tests were performed on the friction material compositions of Nos. 1 to 2 and the disc brake pads. Table 3 shows the test results. The test conditions are as follows.
【0027】(1) 効きレベル JASO C402に従ってダイナモ試験を行い、車速
50km/h条件の摩擦係数(μ平均値)とフェード条
件の摩擦係数(最低μ)を比較した。 (2) ブレーキ鳴き JASO C402に従って実車試験を行い、試験中の
ブレーキ鳴きを測定し、75dB以上のブレーキ鳴きの
発生率を求めた。(1) Effectiveness level A dynamo test was conducted in accordance with JASO C402, and the friction coefficient (μ average value) under a vehicle speed of 50 km / h was compared with the friction coefficient (minimum μ) under a fade condition. (2) Brake squeal An actual vehicle test was performed according to JASO C402, the brake squeal during the test was measured, and the occurrence rate of brake squeal of 75 dB or more was determined.
【0028】(3) パッド摩耗量、相手材摩耗量 上記(1)の試験において、試験後の摩耗量を求めた。 (4) 金属繊維の脱落 摩擦材組成物をそれぞれ別々にポリエチレン製の袋に入
れ、10回振りその袋の下部に脱落した金属繊維の量を
測定することで評価した。なお、上記(1)〜(3)の
試験は全て日産自動車株式会社製、車種名:プリメーラ
のブレーキユニットを用いて行った。(3) Pad wear and mating material wear In the above test (1), the wear after the test was determined. (4) Dropping of Metal Fibers Each friction material composition was separately put into a polyethylene bag, shaken 10 times, and the amount of the metal fiber dropped at the bottom of the bag was evaluated. The tests (1) to (3) were all performed using Nissan Motor Co., Ltd., model name: Primera brake unit.
【0029】[0029]
【表3】 [Table 3]
【0030】表3に示されるように、本発明の実施例に
なる摩擦材組成物は、金属繊維の脱落が少なく、許容レ
ベルであり、また本発明の実施例になる摩擦材組成物を
用いたディスブレーキパッドは、効きレベルが高く、ブ
レーキ鳴きとパッド摩耗量及び相手材摩耗量が少ないこ
とが明らかである。これに対して比較例の摩擦材組成物
は金属繊維の脱落が少なく、許容レベルであったが、比
較例1の摩擦材組成物を用いたディスクブレーキパッド
は効きレベルが低く、パッド摩耗量が多く、また比較例
2の摩擦材組成物を用いたディスクブレーキパッドはブ
レーキ鳴きと相手材摩耗量が多かった。As shown in Table 3, the friction material composition according to the example of the present invention has a small amount of metal fibers and has an acceptable level, and the friction material composition according to the example of the present invention is used. It is evident that the used brake pad has a high effectiveness level, and the brake squeal, the pad wear amount and the mating material wear amount are small. On the other hand, the friction material composition of the comparative example had a low level of metal fiber detachment and was at an acceptable level, whereas the disc brake pad using the friction material composition of Comparative Example 1 had a low effectiveness level and had a low pad wear amount. The disc brake pad using the friction material composition of Comparative Example 2 had a large amount of brake squeal and abrasion of the mating material.
【0031】[0031]
【発明の効果】請求項1及び2における摩擦材組成物
は、金属繊維の脱落と偏析が少なく、金属繊維の酸化劣
化を抑え、音振性能、効き及び耐摩耗性に優れた摩擦材
を提供することができる。請求項3の方法により得られ
る摩擦材組成物は、金属繊維の脱落と偏析が少なく、金
属繊維の酸化劣化を抑え、音振性能、効き及び耐摩耗性
に優れた摩擦材を提供することができる。請求項4にお
ける摩擦材は、金属繊維の酸化劣化を抑え、音振性能、
効き及び耐摩耗性に優れ、工業的に極めて好適である。The friction material composition according to the first and second aspects provides a friction material which is less likely to fall off and segregate metal fibers, suppresses oxidative deterioration of metal fibers, and is excellent in sound vibration performance, effectiveness and wear resistance. can do. The friction material composition obtained by the method according to the third aspect provides a friction material which has less falling off and segregation of metal fibers, suppresses oxidative deterioration of metal fibers, and has excellent sound vibration performance, effectiveness and wear resistance. it can. The friction material according to claim 4 suppresses oxidative deterioration of the metal fiber, and has a sound vibration performance,
It is excellent in efficacy and abrasion resistance and is industrially extremely suitable.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) F16D 69/02 F16D 69/02 E // C08L 61:06 C08L 61:06 Fターム(参考) 3J058 BA21 FA01 FA11 FA21 GA03 GA04 GA07 GA14 GA20 GA23 GA24 GA29 GA33 GA34 GA43 GA45 GA73 4F071 AA01 AA10 AA41 AA56 AA74 AB03 AB06 AB08 AB12 AB18 AB23 AB24 AB30 AD01 AE12 AH07 DA04 DA05 DA10 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification symbol FI theme coat ゛ (reference) F16D 69/02 F16D 69/02 E // C08L 61:06 C08L 61:06 F term (reference) 3J058 BA21 FA01 FA11 FA21 GA03 GA04 GA07 GA14 GA20 GA23 GA24 GA29 GA33 GA34 GA43 GA45 GA73 4F071 AA01 AA10 AA41 AA56 AA74 AB03 AB06 AB08 AB12 AB18 AB23 AB24 AB30 AD01 AE12 AH07 DA04 DA05 DA10
Claims (4)
摩擦材組成物において、表面がブチルゴム、シリコーン
ゴム、フッ素ゴムのうち1種類以上のエラストマーで被
覆された金属繊維を10〜50重量%含有してなる摩擦
材組成物。1. A friction material composition containing a fibrous substance, a binder and a friction modifier, wherein 10 to 50% by weight of a metal fiber whose surface is coated with one or more elastomers of butyl rubber, silicone rubber and fluorine rubber. % Friction material composition.
対して2〜15重量部である請求項1記載の摩擦材組成
物。2. The friction material composition according to claim 1, wherein the amount of the elastomer is 2 to 15 parts by weight based on 100 parts by weight of the metal fiber.
フッ素ゴムのうち1種類以上のエラストマーで被覆した
後、他の繊維状物質、結合剤及び摩擦調整剤を含む材料
を添加し、混合することを特徴とする摩擦材組成物の製
造法。3. The metal fiber is made of butyl rubber, silicone rubber,
A method for producing a friction material composition, comprising coating with at least one elastomer among fluororubbers, adding a material containing another fibrous substance, a binder and a friction modifier, and mixing.
は請求項3記載の方法で製造された摩擦材組成物を加熱
加圧成形してなる摩擦材。4. A friction material formed by heating and pressing the friction material composition according to claim 1 or 2 or the friction material composition produced by the method according to claim 3.
Priority Applications (1)
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---|---|---|---|
JP2001114365A JP2002309234A (en) | 2001-04-12 | 2001-04-12 | Friction material composition, manufacturing method of the same and friction material using the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2001114365A JP2002309234A (en) | 2001-04-12 | 2001-04-12 | Friction material composition, manufacturing method of the same and friction material using the same |
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Publication Number | Publication Date |
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JP2002309234A true JP2002309234A (en) | 2002-10-23 |
Family
ID=18965451
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110922758A (en) * | 2019-10-28 | 2020-03-27 | 建湖金洋科技有限公司 | Rail shock absorption base plate |
-
2001
- 2001-04-12 JP JP2001114365A patent/JP2002309234A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110922758A (en) * | 2019-10-28 | 2020-03-27 | 建湖金洋科技有限公司 | Rail shock absorption base plate |
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