WO2017183439A1 - 摩擦材 - Google Patents
摩擦材 Download PDFInfo
- Publication number
- WO2017183439A1 WO2017183439A1 PCT/JP2017/014028 JP2017014028W WO2017183439A1 WO 2017183439 A1 WO2017183439 A1 WO 2017183439A1 JP 2017014028 W JP2017014028 W JP 2017014028W WO 2017183439 A1 WO2017183439 A1 WO 2017183439A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- friction
- mass
- friction material
- titanate
- crystal structure
- 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.)
- Ceased
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Classifications
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16D—COUPLINGS FOR TRANSMITTING ROTATION; CLUTCHES; BRAKES
- F16D69/00—Friction linings; Attachment thereof; Selection of coacting friction substances or surfaces
- F16D69/02—Composition of linings ; Methods of manufacturing
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16D—COUPLINGS FOR TRANSMITTING ROTATION; CLUTCHES; BRAKES
- F16D69/00—Friction linings; Attachment thereof; Selection of coacting friction substances or surfaces
- F16D69/02—Composition of linings ; Methods of manufacturing
- F16D69/027—Compositions based on metals or inorganic oxides
- F16D69/028—Compositions based on metals or inorganic oxides containing fibres
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16D—COUPLINGS FOR TRANSMITTING ROTATION; CLUTCHES; BRAKES
- F16D69/00—Friction linings; Attachment thereof; Selection of coacting friction substances or surfaces
- F16D69/02—Composition of linings ; Methods of manufacturing
- F16D69/025—Compositions based on an organic binder
- F16D69/026—Compositions based on an organic binder containing fibres
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/14—Anti-slip materials; Abrasives
- C09K3/149—Antislip compositions
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16D—COUPLINGS FOR TRANSMITTING ROTATION; CLUTCHES; BRAKES
- F16D2200/00—Materials; Production methods therefor
- F16D2200/0034—Materials; Production methods therefor non-metallic
- F16D2200/0039—Ceramics
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16D—COUPLINGS FOR TRANSMITTING ROTATION; CLUTCHES; BRAKES
- F16D2200/00—Materials; Production methods therefor
- F16D2200/006—Materials; Production methods therefor containing fibres or particles
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16D—COUPLINGS FOR TRANSMITTING ROTATION; CLUTCHES; BRAKES
- F16D2200/00—Materials; Production methods therefor
- F16D2200/006—Materials; Production methods therefor containing fibres or particles
- F16D2200/0073—Materials; Production methods therefor containing fibres or particles having lubricating properties
Definitions
- the present invention relates to a friction material made of a friction material composition of NAO (Non-Asbestos-Organic) material used for a disc brake pad of an automobile or the like.
- NAO Non-Asbestos-Organic
- a disc brake is used as a braking device for an automobile, and a disc brake pad in which a friction material is attached to a metal base member is used as the friction member.
- the friction material composition of the NAO material includes a binder, a fiber base material other than steel fibers such as steel fibers and stainless fibers, a friction adjusting material, a lubricant, a pH adjusting material, and a filler.
- titanates such as potassium titanate, lithium potassium titanate, and magnesium potassium titanate have been widely used as friction modifiers.
- Patent Document 1 discloses a friction material that does not contain a metal fiber and a copper component, and includes 10 to 35% by volume of potassium titanate having a plurality of convex shapes, and 3 to 10% by volume of an abrasive having a Mohs hardness of 7 or more. And a friction material containing 10-30% by volume of an elastomer-modified phenol resin.
- Patent Document 2 discloses a friction material composition including a binder, an organic filler, an inorganic filler, and a fiber base material, and the content of copper in the friction material composition is 5% by mass or less as a copper element.
- the content of metal fibers other than copper and copper alloy is 0.5 mass% or less, contains titanate and antimony trisulfide, and the titanate is lithium potassium titanate or magnesium potassium titanate.
- a non-asbestos friction material composition having a titanate content of 14 to 20% by mass and an antimony trisulfide content of 2 to 6% by mass, and a friction molded from the friction material composition The materials are listed.
- Patent Document 1 and Patent Document 2 have a problem that the required performance of brake effectiveness, crack resistance, and fade resistance cannot be satisfied.
- the titanate used for the friction material includes a tunnel crystal structure titanate and a layer crystal structure titanate.
- the tunnel crystal structure titanate include potassium titanate, 8
- the titanate having a layered crystal structure such as potassium titanate and sodium hexatitanate, lithium potassium titanate, magnesium potassium titanate and the like are used.
- a titanate has the characteristic of eluting an alkali.
- Patent Document 3 has the following description about the alkali elution rate of titanate.
- the alkali elution rate of the titanate compound may be 15% by mass or less, preferably 0.1 to 15% by mass, more preferably 0.1 to 10% by mass, and further preferably 0.1 to 6% by mass.
- By using such a titanate compound it is possible to suppress the fade phenomenon and improve the wear resistance.
- Alkali components generated by the abrasion destruction of the titanate compound are decomposed gases and transfer of organic components. It is presumed that it is acting on the formation of the film (transfer film).
- an alkali elution rate means the mass ratio of the alkali metal and alkaline-earth metal which eluted in the water from the titanate compound in 80 degreeC water.
- Patent Document 3 describes the alkali elution rate of titanate without distinguishing between titanates having a layered crystal structure and titanates having a tunnel-like crystal structure. It is known that the titration rate of the alkali is different between the titanate having a crystal structure and the titanate having a layered crystal structure in which alkali is easily eluted.
- the alkali elution rate of titanates generally used for friction materials is less than 2.0% by mass for titanates having a tunnel crystal structure, and 2.6% for titanates having a layered crystal structure. It is at least mass%.
- Table 1 shows the titanate crystal structures and alkali elution rates described in Patent Document 3 and Patent Document 4.
- titanates having a layered crystal structure have not been studied so far.
- JP 2014-122314 A Japanese Unexamined Patent Publication No. 2016-824 JP 2014-224175 A JP 2014-189612 A
- the present invention relates to a friction material comprising a friction material composition of NAO material including a binding material, a fiber base material, a friction adjusting material, a lubricant, a pH adjusting material, and a filler used for a disc brake pad. It is an object of the present invention to provide a friction material that satisfies the required performance of crack resistance and fade resistance.
- the present inventors have determined from a friction material composition of NAO material including a binding material, a fiber base material, a friction adjusting material, a lubricant, a pH adjusting material, and a filler used for a disc brake pad.
- the alkali elution rate of the layered crystal structure titanate is 0.1% by mass or more and 2.5% by mass or less, preferably 0.5% by mass or more and 1.5% by mass or less.
- the present invention is a friction material comprising a friction material composition of NAO material including a binding material, a fiber base material, a friction adjusting material, a lubricant, a pH adjusting material, and a filler used for a disc brake pad, It is based on this technology.
- a friction material comprising a friction material composition of NAO material including a binder, a fiber base material, a friction adjusting material, a lubricant, a pH adjusting material, and a filler used for a disc brake pad, and the friction material
- the composition comprises a friction material containing 5 to 30% by mass of a titanate having a layered crystal structure having an alkali elution rate of 0.1% by mass or more and 2.5% by mass or less as a friction modifier based on the total amount of the friction material composition.
- the friction material composition comprises a monoclinic zirconium oxide as a friction modifier in an amount of 5 to 25% by mass based on the total amount of the friction material composition, and a fibrillated organic fiber as a fiber base material.
- the friction material according to any one of (1) to (3), which is contained in an amount of 1 to 5% by mass based on the total amount.
- a friction material comprising a friction material composition of NAO material including a binding material, a fiber base material, a friction adjusting material, a lubricant, a pH adjusting material, and a filler, used for a disc brake pad. It is possible to provide a friction material that satisfies the required performance of the effect, crack resistance, and fade resistance.
- a friction adjusting material used for a disc brake pad is a friction material comprising a friction material composition of NAO material including a binder, a fiber base material, a friction adjusting material, a lubricant, a pH adjusting material, and a filler.
- a friction material composition a titanate having a layered crystal structure having an alkali elution rate of 0.1% by mass or more and 2.5% by mass or less is contained in an amount of 5 to 30% by mass based on the total amount of the friction material composition.
- the titanate having a layered crystal structure is more likely to form a stable film on the sliding surface of the counterpart material than the titanate having a tunnel crystal structure.
- the curing reaction of the thermosetting resin that is a binder is inhibited at the time of heat and pressure molding.
- the alkali elution rate of the titanate having a layered crystal structure is particularly preferably in the range of 0.5 to 1.5% by mass.
- titanate having a layered crystal structure one or a combination of two selected from magnesium potassium titanate and lithium potassium titanate can be used. In order to further improve the fade resistance, it is preferable to use magnesium potassium titanate having high heat resistance alone.
- monoclinic zirconium oxide as a friction modifier is 5 to 25% by mass with respect to the total amount of the friction material composition
- fibrillated organic fiber is 1 to 5% with respect to the total amount of the friction material composition as a fiber base material.
- Monoclinic zirconium oxide has the property of phase transition to tetragonal with volume shrinkage at high temperatures. Therefore, at high temperature and high load, zirconium oxide undergoes phase transition, shrinks its volume, and easily falls off from the matrix. The dropped zirconium oxide is supplied to the friction surface, and the abrasive action of the zirconium oxide accelerates the abrasion destruction of the titanate having a layered crystal structure, and the alkali component is released from the titanate.
- the average particle diameter is a numerical value of 50% particle diameter measured by a laser diffraction particle size distribution method.
- the fibrillated organic fibers one or a combination of two or more selected from aramid fibers, cellulose fibers, and polyacrylonitrile fibers can be used. In order to further improve the crack resistance, it is preferable to use an aramid fiber having a high reinforcing effect alone.
- the friction material of the present invention includes a binder, a fiber base, and friction adjustment that are usually used for friction materials. It consists of a friction material composition containing a material, a lubricant, a pH adjusting material, and a filler.
- binder straight phenol resin, resin modified with various elastomers such as cashew oil, acrylic rubber, silicone rubber, aralkyl modified phenol resin obtained by reacting phenols, aralkyl ethers and aldehydes, Examples thereof include binders commonly used for friction materials such as thermosetting resins in which various elastomers and fluoropolymers are dispersed in phenol resins, and these can be used alone or in combination of two or more.
- elastomers such as cashew oil, acrylic rubber, silicone rubber, aralkyl modified phenol resin obtained by reacting phenols, aralkyl ethers and aldehydes
- binders commonly used for friction materials such as thermosetting resins in which various elastomers and fluoropolymers are dispersed in phenol resins, and these can be used alone or in combination of two or more.
- the content of the binder is preferably 7 to 15% by mass, more preferably 8 to 12% by mass with respect to the total amount of the friction material composition in order to ensure sufficient mechanical strength and wear resistance. preferable.
- the fiber base material examples include metal fibers such as copper fibers, bronze fibers, brass fibers, aluminum fibers, and aluminum alloy fibers in addition to the above-described fibrillated organic fibers. Two or more kinds can be used in combination.
- the content of the fiber base material is preferably 2 to 20% by mass, preferably 3 to 15% by mass, based on the total amount of the friction material composition together with the fibrillated organic fibers. Is more preferable.
- inorganic friction modifiers include stabilized zirconium oxide, zirconium silicate, magnesium oxide, ⁇ -alumina, ⁇ -alumina, talc, in addition to the layered crystal structure of titanate and monoclinic zirconium oxide.
- Mica vermiculite, zinc particles, copper particles, brass particles, aluminum particles, aluminum alloy particles, particulate inorganic friction modifier such as tunnel crystal structure titanate, wollastonite, sepiolite, basalt fiber, glass fiber,
- fibrous inorganic friction modifiers such as biosoluble ceramic fibers and rock wool, and these can be used alone or in combination of two or more.
- the content of the inorganic friction modifier is preferably 30 to 70% by mass, based on the total amount of the friction material composition, including the titanate having the layered crystal structure and monoclinic zirconium oxide, and preferably 40 to 60%. It is more preferable to set it as the mass%.
- Organic friction modifiers are usually used for friction materials such as cashew dust, pulverized tire tread rubber, vulcanized rubber powder such as nitrile rubber, acrylic rubber, butyl rubber, and silicone rubber, or unvulcanized rubber powder. These organic friction modifiers can be used, and these can be used alone or in combination of two or more.
- the content of the organic friction modifier is preferably 3 to 8% by mass, more preferably 4 to 7% by mass, based on the total amount of the friction material composition.
- Lubricants include metal sulfide lubricants such as zinc sulfide, molybdenum disulfide, tin sulfide, iron sulfide, and composite metal sulfides, artificial graphite, natural graphite, flake graphite, petroleum coke, elastic graphitized carbon, Lubricants usually used for friction materials such as carbonaceous lubricants such as oxidized polyacrylonitrile fiber pulverized powder can be mentioned, and these can be used alone or in combination of two or more.
- metal sulfide lubricants such as zinc sulfide, molybdenum disulfide, tin sulfide, iron sulfide, and composite metal sulfides, artificial graphite, natural graphite, flake graphite, petroleum coke, elastic graphitized carbon, Lubricants usually used for friction materials such as carbonaceous lubricants such as oxidized polyacrylonitrile fiber pulverized powder can be mentioned,
- the lubricant content is preferably 3 to 8% by mass, more preferably 4 to 6% by mass, based on the total amount of the friction material composition.
- the pH adjusting material a pH adjusting material usually used for friction materials such as calcium hydroxide can be used.
- the pH adjuster is preferably 2 to 6% by mass, more preferably 2 to 3% by mass, based on the total amount of the friction material composition.
- barium sulfate As the filler, barium sulfate, calcium carbonate, etc. are used.
- the friction material of the present invention comprises a mixing step in which a predetermined amount of the friction material composition is uniformly mixed using a mixer, and the resulting friction material raw material mixture is separately cleaned and surface-treated separately,
- the applied back plate is overlaid and put into a thermoforming mold, and heated and pressed to form by heating and pressurization, the resulting molded product is heated to complete the curing reaction of the binder, spray coating, It is manufactured through a painting process in which paint is applied by electrostatic powder coating, a paint baking process in which paint is baked, and a polishing process in which a friction surface is formed by a rotating grindstone.
- the coating process, the heat treatment process also serving as paint baking, and the polishing process are performed in this order.
- granulation step for granulating the friction material raw material mixture, kneading step for kneading the friction material raw material mixture, granulation obtained in the friction material raw material mixture or granulation step The preform and the kneaded product obtained in the kneading process are put into a preforming mold, and a preforming process for molding the preform is performed, and the scorch process is performed after the heat and pressure molding process.
- Friction material compositions having the compositions shown in Tables 2 to 4 were mixed for 5 minutes with a Redige mixer, and pre-molded by pressing at 30 MPa in a molding die for 10 seconds. This preform is placed on a steel back plate that has been washed, surface-treated, and coated with an adhesive, and molded in a thermoforming mold at a molding temperature of 150 ° C. and a molding pressure of 40 MPa for 10 minutes, and then 200 Heat treatment (post-curing) was carried out at 5 ° C. for 5 hours, and polishing was performed to form a friction surface, thereby producing disc brake pads for passenger cars (Examples 1 to 19 and Comparative Examples 1 to 4).
- the friction material satisfying the conditions of the present invention has good braking effectiveness, crack resistance, and fade resistance.
- the brake effect, crack resistance, and fade resistance are satisfied while satisfying the laws and regulations concerning the content of the copper component. Therefore, it is possible to provide a friction material that satisfies the required performance, and has a very high practical value.
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- General Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
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Abstract
Description
そして、チタン酸塩はアルカリを溶出するという特性を持つことが知られている。
「チタン酸塩化合物のアルカリ溶出率は15質量%以下であればよく、好ましくは0.1~15質量% 、より好ましくは0.1~10質量% 、さらに好ましくは0.1~6質量%である。このようなチタン酸塩化合物を用いることによりフェード現象を抑制し、耐摩耗性を向上することができる。チタン酸塩化合物の摩滅破壊により生ずるアルカリ成分が、有機成分の分解ガスやトランスファーフィルム(移着膜)の生成に作用しているものと推測される。」
なお、アルカリ溶出率とは、80℃の水中においてチタン酸塩化合物から水中に溶出したアルカリ金属及びアルカリ土類金属の質量割合のことをいう。
層状結晶構造のチタン酸塩のアルカリ溶出率は0.5~1.5質量%の範囲が特に好ましい。
そのため、高温高負荷時、酸化ジルコニウムは相転移して体積が収縮し、マトリックスから脱落しやすくなる。
脱落した酸化ジルコニウムが摩擦面に供給され、酸化ジルコニウムの研削作用により、層状結晶構造のチタン酸塩の摩滅破壊が促進され、チタン酸塩からアルカリ成分が放出される。
摩擦材内部に吸収された水分によって層状結晶構造のチタン酸塩のアルカリ成分が溶出しやすくなる。
なお、平均粒子径は、レーザー回折粒度分布法により測定した50%粒径の数値である。
pH調整材は、摩擦材組成物全量に対して2~6質量%とするのが好ましく、2~3質量%とするのがより好ましい。
必要に応じて、加熱加圧成型工程の前に、摩擦材原料混合物を造粒する造粒工程、摩擦材原料混合物を混練する混練工程、摩擦材原料混合物又は造粒工程で得られた造粒物、混練工程で得られた混練物を予備成型型に投入し、予備成型物を成型する予備成型工程が実施され、加熱加圧成型工程の後にスコーチ工程が実施される。
表2~表4に示す組成の摩擦材組成物をレディゲミキサーにて5分間混合し、成型金型内で30MPaにて10秒間加圧して予備成型をした。この予備成型物を、予め洗浄、表面処理、接着材を塗布した鋼鉄製のバックプレート上に重ね、熱成型型内で成型温度150℃、成型圧力40MPaの条件下で10分間成型した後、200℃で5時間熱処理(後硬化)を行い、研磨して摩擦面を形成し、乗用車用ディスクブレーキパッドを作製した(実施例1~19、比較例1~4)。
Claims (4)
- ディスクブレーキパッドに使用される、結合材、繊維基材、摩擦調整材、潤滑材、pH調整材、充填材を含むNAO材の摩擦材組成物から成る摩擦材であり、前記摩擦材組成物は、摩擦調整材としてアルカリ溶出率が0.1質量%以上2.5質量%以下の層状結晶構造のチタン酸塩を摩擦材組成物全量に対し5~30質量%含有することを特徴とする摩擦材。
- 前記層状結晶構造のチタン酸塩のアルカリ溶出率が0.5質量%以上1.5質量%以下であることを特徴とする請求項1に記載の摩擦材。
- 前記層状結晶構造のチタン酸塩がチタン酸マグネシウムカリウムであることを特徴とする請求項1又は請求項2に記載の摩擦材。
- 前記摩擦材組成物は、摩擦調整材として単斜晶の酸化ジルコニウムを摩擦材組成物全量に対し5~25質量%と、繊維基材としてフィブリル化された有機繊維を摩擦材組成物全量に対し1~5質量%含有することを特徴とする請求項1~3のいずれかに記載の摩擦材。
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16/164,743 US20190154094A1 (en) | 2016-04-19 | 2017-04-04 | Friction material |
| KR1020187031729A KR102347391B1 (ko) | 2016-04-19 | 2017-04-04 | 마찰재 |
| CN201780024347.1A CN109072047A (zh) | 2016-04-19 | 2017-04-04 | 摩擦材料 |
| EP17785781.0A EP3447103B1 (en) | 2016-04-19 | 2017-04-04 | Friction material |
| CN202311828792.7A CN117869500A (zh) | 2016-04-19 | 2017-04-04 | 摩擦材料 |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2016-083851 | 2016-04-19 | ||
| JP2016083851A JP6301997B2 (ja) | 2016-04-19 | 2016-04-19 | 摩擦材 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2017183439A1 true WO2017183439A1 (ja) | 2017-10-26 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2017/014028 Ceased WO2017183439A1 (ja) | 2016-04-19 | 2017-04-04 | 摩擦材 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20190154094A1 (ja) |
| EP (1) | EP3447103B1 (ja) |
| JP (1) | JP6301997B2 (ja) |
| KR (1) | KR102347391B1 (ja) |
| CN (2) | CN109072047A (ja) |
| WO (1) | WO2017183439A1 (ja) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN114174692A (zh) * | 2019-07-23 | 2022-03-11 | 日清纺制动器株式会社 | 摩擦材料 |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP7323309B2 (ja) * | 2019-03-20 | 2023-08-08 | 曙ブレーキ工業株式会社 | ディスクブレーキ用摩擦材 |
| WO2021010003A1 (ja) * | 2019-07-18 | 2021-01-21 | 日清紡ブレーキ株式会社 | 摩擦材組成物、摩擦材及びディスクブレーキパッド |
| JP7344694B2 (ja) | 2019-07-23 | 2023-09-14 | 日清紡ブレーキ株式会社 | 摩擦材 |
| CN115698218B (zh) * | 2020-06-16 | 2025-03-14 | 日清纺制动器株式会社 | 摩擦副 |
| EP4166621A4 (en) * | 2020-06-16 | 2024-07-03 | Nisshinbo Brake Inc. | Friction pair |
| CN116234775A (zh) * | 2020-08-04 | 2023-06-06 | 大塚化学株式会社 | 摩擦调整材料、摩擦材料组合物、摩擦材料和摩擦部件 |
| CN121219239A (zh) * | 2023-05-26 | 2025-12-26 | 大塚化学株式会社 | 钛酸镁钾、摩擦调节材料、摩擦材料组合物、摩擦材料和摩擦构件 |
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| JP2002371266A (ja) * | 2001-06-14 | 2002-12-26 | Aisin Seiki Co Ltd | 摩擦材 |
| WO2012066964A1 (ja) * | 2010-11-19 | 2012-05-24 | 日立化成工業株式会社 | ノンアスベスト摩擦材組成物、これを用いた摩擦材及び摩擦部材 |
| WO2014098215A1 (ja) * | 2012-12-21 | 2014-06-26 | 曙ブレーキ工業株式会社 | 摩擦材 |
| JP2014189612A (ja) * | 2013-03-27 | 2014-10-06 | Otsuka Chem Co Ltd | 樹脂組成物、摩擦材及びそれらの製造方法 |
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| JP2015147913A (ja) * | 2014-02-10 | 2015-08-20 | 日本ブレーキ工業株式会社 | 摩擦材組成物、摩擦材組成物を用いた摩擦材及び摩擦部材 |
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| CN102449098B (zh) * | 2009-06-01 | 2015-07-15 | 日立化成株式会社 | 摩擦材料组合物、使用该组合物的摩擦材料以及摩擦部件 |
| JP6157071B2 (ja) | 2011-09-14 | 2017-07-05 | 曙ブレーキ工業株式会社 | 摩擦材 |
| JP5981839B2 (ja) | 2012-12-21 | 2016-08-31 | 曙ブレーキ工業株式会社 | 摩擦材 |
| JP2014148666A (ja) * | 2013-01-11 | 2014-08-21 | Nisshinbo Brake Inc | 摩擦材 |
| JP2014156589A (ja) * | 2013-01-15 | 2014-08-28 | Nisshinbo Brake Inc | 摩擦材 |
| JP5958623B2 (ja) | 2015-08-13 | 2016-08-02 | 日立化成株式会社 | ノンアスベスト摩擦材組成物 |
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| JP2000160135A (ja) * | 1998-11-25 | 2000-06-13 | Hitachi Chem Co Ltd | 摩擦材組成物及び該摩擦材組成物を用いた摩擦材 |
| JP2002371266A (ja) * | 2001-06-14 | 2002-12-26 | Aisin Seiki Co Ltd | 摩擦材 |
| WO2012066964A1 (ja) * | 2010-11-19 | 2012-05-24 | 日立化成工業株式会社 | ノンアスベスト摩擦材組成物、これを用いた摩擦材及び摩擦部材 |
| WO2014098215A1 (ja) * | 2012-12-21 | 2014-06-26 | 曙ブレーキ工業株式会社 | 摩擦材 |
| JP2014189612A (ja) * | 2013-03-27 | 2014-10-06 | Otsuka Chem Co Ltd | 樹脂組成物、摩擦材及びそれらの製造方法 |
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| JP2015147913A (ja) * | 2014-02-10 | 2015-08-20 | 日本ブレーキ工業株式会社 | 摩擦材組成物、摩擦材組成物を用いた摩擦材及び摩擦部材 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN114174692A (zh) * | 2019-07-23 | 2022-03-11 | 日清纺制动器株式会社 | 摩擦材料 |
| US12172926B2 (en) | 2019-07-23 | 2024-12-24 | Nisshinbo Brake, Inc. | Friction material |
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| EP3447103A1 (en) | 2019-02-27 |
| CN109072047A (zh) | 2018-12-21 |
| EP3447103B1 (en) | 2021-08-11 |
| US20190154094A1 (en) | 2019-05-23 |
| CN117869500A (zh) | 2024-04-12 |
| KR20180134936A (ko) | 2018-12-19 |
| KR102347391B1 (ko) | 2022-01-06 |
| JP6301997B2 (ja) | 2018-03-28 |
| EP3447103A4 (en) | 2019-05-01 |
| JP2017193612A (ja) | 2017-10-26 |
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