JP5183902B2 - Non-asbestos friction member - Google Patents
Non-asbestos friction member Download PDFInfo
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- JP5183902B2 JP5183902B2 JP2006269294A JP2006269294A JP5183902B2 JP 5183902 B2 JP5183902 B2 JP 5183902B2 JP 2006269294 A JP2006269294 A JP 2006269294A JP 2006269294 A JP2006269294 A JP 2006269294A JP 5183902 B2 JP5183902 B2 JP 5183902B2
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- asbestos
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- 239000010425 asbestos Substances 0.000 title claims description 21
- 229910052895 riebeckite Inorganic materials 0.000 title claims description 21
- 239000002783 friction material Substances 0.000 claims description 81
- 229920001971 elastomer Polymers 0.000 claims description 26
- 239000000463 material Substances 0.000 claims description 23
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- 238000003856 thermoforming Methods 0.000 description 7
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- 230000002159 abnormal effect Effects 0.000 description 6
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- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 2
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- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
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- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
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- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
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- AFZSMODLJJCVPP-UHFFFAOYSA-N dibenzothiazol-2-yl disulfide Chemical compound C1=CC=C2SC(SSC=3SC4=CC=CC=C4N=3)=NC2=C1 AFZSMODLJJCVPP-UHFFFAOYSA-N 0.000 description 1
- REQPQFUJGGOFQL-UHFFFAOYSA-N dimethylcarbamothioyl n,n-dimethylcarbamodithioate Chemical compound CN(C)C(=S)SC(=S)N(C)C REQPQFUJGGOFQL-UHFFFAOYSA-N 0.000 description 1
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 1
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- AUZONCFQVSMFAP-UHFFFAOYSA-N disulfiram Chemical compound CCN(CC)C(=S)SSC(=S)N(CC)CC AUZONCFQVSMFAP-UHFFFAOYSA-N 0.000 description 1
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- 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
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- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
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- 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
- 239000010680 novolac-type phenolic resin Substances 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
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Description
本発明は、自動車、鉄道車両、産業機械等のブレーキ等に使用される摩擦部材に関し、特に、フェード特性と鳴き特性を両立させた摩擦部材に関するものであり、より具体的には前記の用途に使用されるブレーキパッド、ブレーキライニング、クラッチフェーシング等に関するものである。 The present invention relates to a friction member used for brakes of automobiles, railway vehicles, industrial machines, etc., and more particularly to a friction member having both fading characteristics and squeal characteristics. It relates to used brake pads, brake linings, clutch facings, etc.
従来、摩擦材は、繊維基材、摩擦調整材、充填材及び結合材を用い、それらを配合し、予備成形、熱成形、仕上げなどの工程からなる製造プロセスによって製造されている。しかし、公害防止等のため摩擦材のノンアスベスト化が進むにつれて使用可能な材料が限定されるようになってきており、ノンアスベスト摩擦材に含有される無機充填材においても粉状の材料の使用が多くなってきた。このため摩擦材の性状としては硬度が大きく気孔率が小さくなる傾向にある。そして、初期摩擦係数が硬度に依存しているので摩擦特性は低下し、またフェード特性は気孔率に依存しているのでこれらも低下する傾向にあった。これに加えてノイズも発生しやすくなっていた。 Conventionally, a friction material uses a fiber base material, a friction adjusting material, a filler, and a binder, blends them, and is manufactured by a manufacturing process including steps such as preforming, thermoforming, and finishing. However, the use of non-asbestos friction materials has been limited in order to prevent pollution, etc., and the use of powdered materials has been limited for inorganic fillers contained in non-asbestos friction materials. Has increased. For this reason, the friction material tends to have a high hardness and a low porosity. Since the initial friction coefficient depends on the hardness, the friction characteristic is lowered, and since the fade characteristic is dependent on the porosity, these tend to be lowered. In addition to this, noise was easily generated.
上記のような欠点を改善し、制動時の鳴きや、異音の発生しない摩擦材を提供するために、「特許文献1」では、補強繊維と無機及び有機充填材と結合材樹脂とを混合した摩擦材原料を、金型とパッド裏板間に作成されるキャビティ内に摩擦材厚み方向に複数層に分けて投入し、その層分けした原料のうち裏板に接する接着層の原料は造粒材料とし、この造粒材料を含めてキャビティ内の原料を熱圧縮形成後、加熱硬化させて、摩擦材が気孔率の小さな接着層と気孔率の大きな母材層のを積層構造からなるディスクブレーキパッドを製造している。その結果、裏板の錆発生を防ぎ、接着力が高まるほか、摩擦材の層間強度も向上し、信頼性の高いディスクブレーキパッドを得られると記載している。 In order to improve the above drawbacks and provide a friction material that does not generate noise or noise during braking, in “Patent Document 1”, a reinforcing fiber, an inorganic and organic filler, and a binder resin are mixed. The friction material raw material is injected into a cavity created between the mold and the pad back plate in multiple layers in the thickness direction of the friction material, and the raw material for the adhesive layer in contact with the back plate is granulated. A disk brake consisting of a laminated structure consisting of an adhesive layer with a low porosity and a base material layer with a high porosity. Manufactures pads. As a result, it is described that the rust generation of the back plate is prevented, the adhesive strength is increased, the interlayer strength of the friction material is also improved, and a highly reliable disc brake pad can be obtained.
「特許文献2」においては、平均粒径が2.5〜11mmの、結合材と無機繊維からなる造粒物を摩擦材組成物に対して5〜30容量%含有する摩擦材は、耐フェード特性に優れ、かつ制動時の鳴きや、異音が殆ど発生しないと述べている。
又、「特許文献3」は、平均粒径が2.5〜11mmの、結合材と無機繊維及びNBR、SBRのようなゴム粉末からなる造粒物を摩擦材組成物に対して「特許文献2」と同じ配合量にすると同様な作用効果が得られると報告している。
In “
In addition, “
又、「特許文献4」では、表面がブチルゴム、シリコンゴム、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%含有する摩擦材が記されている。前記の摩擦材は、エラストマーを金属繊維100重量部に対して2〜15重量部配合した場合、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、異音性能及び耐摩耗性に優れた摩擦材として使用される。
しかしながら、いずれの場合も、鳴き特性、耐摩耗性及びフェード特性等の摩擦材に必要な目標性能をバランスよく満足させることは困難であった。
However, in any case, it has been difficult to satisfy the target performance necessary for the friction material such as squealing characteristics, wear resistance, and fading characteristics in a balanced manner.
車両のブレーキに対しては、燃費向上やハンドリング特性向上のためバネ下荷重低減策として、一般的にシステムを含めたブレーキを小型化する要求がでてきている。一方で、小型化にあたっては、ブレーキの効力レベル(摩擦材の効きレベル)を上げることが必要になる。ただし、ブレーキの効力レベル(摩擦材の効きレベル)を上げることは、研削性を上げる方向になり、一般的に、鳴き、ジャダー特性の劣化傾向になってしまうため、高い効きレベルと鳴き、ジャダー性の商品性の両立が困難である。それを改善するためにゴム系の材料を配合することにより改善効果を得られるが、配合すると摩擦材としての耐熱性が低下し高速、高温での効き、耐フェード性の低下につながってしまう。 With respect to vehicle brakes, as a measure for reducing unsprung loads in order to improve fuel efficiency and handling characteristics, there is a demand for reducing the size of the brake including the system. On the other hand, for downsizing, it is necessary to increase the braking effectiveness level (the friction material effectiveness level). However, increasing the brake effectiveness level (the friction material effectiveness level) tends to increase the grindability, and generally tends to cause squeal and judder characteristics to deteriorate. It is difficult to achieve both merchandise and sexiness. In order to improve it, an improvement effect can be obtained by blending a rubber-based material, but if blended, the heat resistance as a friction material is lowered, leading to high speed, high temperature effect, and fade resistance.
又、近年、摩擦材はノンアスベスト化に伴って無機フィラーの使用比率が増加した結果、摩擦性能等の特性に関して、所望の性質の成形品を得ることが困難であるという問題が生じてきた。
実際、ディスクブレーキ、ドラムブレーキ共にノンアスベスト系摩擦材が多く使用されているが、問題点の一つとして制動時に鳴きと呼ばれる不快な音を発生することがある。
鳴き発生の原因は主にブレーキ制動時における摩擦材とディスクロータ及びドラムの摩擦振動であると考えられており、この鳴きを防止するために振動特性の良好な組成としたものを摩擦材の一部に設けた複合摩擦材や、摩擦材表面の硬度分布を工夫して摩擦振動が起こりにくい硬度分布にした摩擦材が考えられているが、製造コストが高い等の問題がある。
従って、本発明が解決しようとする課題は、ノンアスベスト系摩擦材において摩擦摩耗性能等の摩擦材自体の性能を損なうことなく、良好な鳴き、異音特性を持つノンアスベスト摩擦材を提供することである。
Further, in recent years, as the friction material has become non-asbestos, the use ratio of the inorganic filler has increased. As a result, there has been a problem that it is difficult to obtain a molded product having desired properties with respect to characteristics such as friction performance.
In fact, many non-asbestos friction materials are used for both disc brakes and drum brakes. However, one of the problems is that unpleasant noise called squeal is generated during braking.
The cause of squeal is thought to be mainly due to frictional vibration between the friction material and the disk rotor and drum during brake braking. To prevent this squeal, a composition with good vibration characteristics is used as one of the friction materials. Although the composite friction material provided in the part and the friction material with the hardness distribution on the surface of the friction material devised to make the friction distribution difficult to cause friction vibration are considered, there are problems such as high manufacturing cost.
Therefore, the problem to be solved by the present invention is to provide a non-asbestos friction material having good squealing and abnormal noise characteristics without impairing the performance of the friction material itself such as friction wear performance in the non-asbestos friction material. It is.
本発明は、下記の手段により上記の課題を解決した。
(1)熱硬化性樹脂結合材、補強繊維及び摩擦調整材を含む摩擦材とプレッシャプレートとが接着されたノンアスベスト摩擦部材において、前記摩擦材は、その接着面から有効摩耗代までの厚み部分に、エラストマー及び架橋剤を含む材料を加熱攪拌して得たプレミックス粒子が30〜40vol%更に配合されていることを特徴とするノンアスベスト摩擦部材。
(2)前記プレミックス粒子が、エラストマー、架橋剤及び補強繊維を含む材料を加熱攪拌して得たものである前記(1)記載のノンアスベスト摩擦部材。
(3)前記プレミックス粒子がエラストマーを10〜97vol%含むことを特徴とする前記(1)又は(2)記載のノンアスベスト摩擦部材。
(4)エラストマー及び架橋剤を含む材料を加熱攪拌して得られたプレミックス粒子を、熱硬化性樹脂結合材、補強繊維及び摩擦調整材を含む摩擦材料に配合した摩擦材原料と、該プレミックス粒子を配合しない摩擦材原料を金型に積層して予備成形した後、熱処理を行うことを特徴とする前記(1)記載のノンアスベスト摩擦部材の製造方法。
The present invention has solved the above problems by the following means.
(1) In a non-asbestos friction member in which a friction material including a thermosetting resin binder, a reinforcing fiber, and a friction modifier and a pressure plate are bonded, the friction material has a thickness portion from the bonding surface to an effective wear allowance. A non-asbestos friction member characterized by further containing 30 to 40 vol% of premix particles obtained by heating and stirring a material containing an elastomer and a crosslinking agent.
(2) The non-asbestos friction member according to (1), wherein the premix particles are obtained by heating and stirring a material containing an elastomer, a crosslinking agent, and reinforcing fibers.
(3) The non-asbestos friction member according to (1) or (2), wherein the premix particles contain 10 to 97 vol% of an elastomer.
(4) A friction material material in which premix particles obtained by heating and stirring a material containing an elastomer and a crosslinking agent are mixed with a friction material containing a thermosetting resin binder, a reinforcing fiber, and a friction modifier, The method for producing a non-asbestos friction member according to (1), wherein the friction material raw material not containing the mixed particles is laminated on a mold and preformed, followed by heat treatment.
摩擦材のプレッシャプレート側の接着面と摩擦材の有効摩耗代までの厚み部分のみに、摩擦材の材料の他にプレミックスを含む層を設けることにより摩擦材自体の特性を変化させることなく、摩擦材の柔軟性を上げられることになるので、良好な鳴き、異音特性を持った摩擦部材を得ることが出来る。 Without changing the characteristics of the friction material itself by providing a layer containing the premix in addition to the material of the friction material only on the adhesive surface on the pressure plate side of the friction material and the thickness portion up to the effective wear allowance of the friction material, Since the flexibility of the friction material can be increased, it is possible to obtain a friction member having good noise and abnormal noise characteristics.
以下、本発明を図面を参照して詳細に説明する。
図1に示すように、本発明の摩擦部材は、プレッシャプレート2に接する側に、接着面(接着層)3があり、摩擦材6はプレミックス含有部分7及び有効摩耗代5からなる。それに対して、従来からの標準的な摩擦部材は接着面(接着層)3に摩擦材6を設けた構造である。
一般に摩擦材の製造は、摩擦材原料の配合、攪拌、常温における予備成形、熱成形、加熱(アフターキュア)、研磨等の仕上げ加工の各工程を経て行われている。熱成形工程では、結合材を熱による反応で硬化させることにより、摩擦材全体を強固に結合させて一体化させ、強度と硬度をもたせる。又、加熱(アフターキュア)条件も摩擦材の品質に影響を与える。摩擦材の結合材として一般的に用いられているのはノボラック型フェノール樹脂(各種変性タイプを含む)であり、硬化剤としてヘキサメチレンテトラミン等が添加混合されている。この硬化剤は摩擦材原料の配合の際に粉末の状態で結合材のノボラック型フェノール樹脂と共に添加される。また、レゾール型フェノール樹脂も使用される。
Hereinafter, the present invention will be described in detail with reference to the drawings.
As shown in FIG. 1, the friction member of the present invention has an adhesive surface (adhesive layer) 3 on the side in contact with the
In general, the friction material is manufactured through each step of finishing processing such as blending of friction material, stirring, preforming at room temperature, thermoforming, heating (after-cure), and polishing. In the thermoforming process, the binding material is cured by a reaction by heat, so that the entire friction material is firmly bonded and integrated to have strength and hardness. The heating (after cure) conditions also affect the quality of the friction material. A novolak-type phenol resin (including various modified types) is generally used as a binder for the friction material, and hexamethylenetetramine or the like is added and mixed as a curing agent. This curing agent is added together with the novolac type phenolic resin as a binder in a powder state when the friction material is blended. A resol type phenol resin is also used.
ディスクブレーキパッド等に使用される摩擦材は、運動エネルギーを熱エネルギーに変えるため常に熱を発生し高温となる。従って、このような摩擦材には耐熱性、耐摩耗性等が要求されるばかりでなく、温度変化によっても摩擦係数の変化の少ない安定した摩擦特性も要求される。更に、ノイズ(鳴き)やジャダーの発生のないことも必要であり、摩擦材には多項目に及ぶ目標性能を満足することが求められている。 A friction material used for a disc brake pad or the like always generates heat and becomes high temperature in order to change kinetic energy into heat energy. Accordingly, such a friction material is required not only to have heat resistance, wear resistance, etc., but also to have stable friction characteristics with little change in the coefficient of friction even when the temperature changes. Furthermore, it is necessary that noise (squeal) and judder are not generated, and the friction material is required to satisfy target performances over a number of items.
摩擦材は、プレッシャプレートに一体に接着されてディスクブレーキパッドとして用いられる。この接着は従来から一般にプレッシャプレートに接着剤を塗布し、熱成形することによって接着され、フェノール系樹脂、エポキシ系樹脂等の熱硬化性樹脂接着剤、或いは架橋性ゴム系接着剤等が使用されている。なお、この接着剤は、予備成形した摩擦材をプレッシャプレートと共に加圧加熱成形することによって、摩擦材の成形と同時に強力に接着される。 The friction material is integrally bonded to the pressure plate and used as a disc brake pad. This bonding is conventionally performed by applying an adhesive to a pressure plate and thermoforming it, and thermosetting resin adhesives such as phenolic resins and epoxy resins, or crosslinkable rubber adhesives are used. ing. In addition, this adhesive is strongly bonded simultaneously with the molding of the friction material by press-molding the preformed friction material together with the pressure plate.
本発明では、摩擦部材の摩擦材のうち、接着面3(プレッシャプレート側の接着面)から有効摩耗代5までの厚み部分のみに、摩擦材の材料に加えてプレミックス4(ゴム、繊維、黒鉛等の複合物)を2〜40vol%、好ましくは20〜40vol%配合した非石綿系パッド材質であることが特徴である。プレミックス含有部分7の厚みは1〜6mmであり、摩擦材6の有効摩耗代5と同じ接着面2から1〜2mmの範囲が好ましい。
In the present invention, in the friction material of the friction member, only the thickness portion from the adhesive surface 3 (adhesive surface on the pressure plate side) to the effective wear allowance 5 is added to the pre-mix 4 (rubber, fiber, It is characterized by a non-asbestos-based pad material containing 2-40 vol%, preferably 20-40 vol%, of a composite such as graphite. The thickness of the premix-containing portion 7 is 1 to 6 mm, and is preferably in the range of 1 to 2 mm from the same
本発明で使用されるプレミックスの構成材料はエラストマー及び架橋剤であり、さらに繊維を含むことができ、それぞれ摩擦材に使用される一般的な材料を使用することができる。
プレミックスは、シリコンゴム、ブチルゴム、クロロブチルゴム、NBRゴム等や、オレフィン系、塩化ビニル系、スチレン系、ポリエステル系等のエラストマーをベースとし、スチール繊維、アラミド繊維、セルロース繊維、アクリル繊維等の繊維類と、黒鉛等と、イオウ、架橋剤で構成され、ニーダー、バンバリーミキサー等の撹拌機により製造したものを使用する。アラミド繊維を使用する場合、平均直径1〜50μm,平均長さ0.5〜5mm程度のものが好適である。架橋剤としては、エラストマーについて反応により架橋構造を与える物質が用いられるが、ゴムの場合、加硫促進剤が用いられ、その加硫促進剤としては、チアゾール系のMBT、MBTS、ZmMBTや、チウラム系のTMTM、TMTD、TETD(いずれも略号)のような化合物を使用することができる。ベースとなるエラストマー、例えばゴムの含有量は全体の10〜97vol%、好ましくは、20〜50vol%使用する。繊維の含有量は全体の1〜90vol%、好ましくは、3〜70vol%である。加硫促進剤の含有量は全体の0.1〜10vol%、好ましくは、0.5〜5vol%である。本発明で使用されるプレミックスの平均粒度は0.1〜8mm、好ましくは、0.5〜4mmの範囲である。
The constituent materials of the premix used in the present invention are an elastomer and a cross-linking agent, and can further contain fibers, and general materials used for friction materials can be used.
The premix is based on silicon rubber, butyl rubber, chlorobutyl rubber, NBR rubber, etc., and elastomers such as olefin, vinyl chloride, styrene, polyester, and fibers such as steel fiber, aramid fiber, cellulose fiber, and acrylic fiber. , Graphite and the like, sulfur, and a cross-linking agent, which are manufactured with a stirrer such as a kneader or a Banbury mixer. When an aramid fiber is used, those having an average diameter of 1 to 50 μm and an average length of about 0.5 to 5 mm are preferable. As the crosslinking agent, a substance that gives a crosslinked structure by reaction with respect to the elastomer is used. In the case of rubber, a vulcanization accelerator is used, and as the vulcanization accelerator, thiazole-based MBT, MBTS, ZmMBT, thiuram, and the like. Compounds such as TMTM, TMTD, and TETD (all abbreviations) of the system can be used. The content of the base elastomer, such as rubber, is 10 to 97% by volume, preferably 20 to 50% by volume. The fiber content is 1 to 90% by volume, preferably 3 to 70% by volume. The content of the vulcanization accelerator is 0.1 to 10% by volume, preferably 0.5 to 5% by volume. The average particle size of the premix used in the present invention is 0.1 to 8 mm, preferably 0.5 to 4 mm.
本発明で使用されるプレミックスは、定法により造粒し熱処理で硬化させ粒子化することが可能であり、圧縮型、混合型、押出し型などの通常の造粒機を使用して造粒粒子化することができる。造粒の際、ゴムの配合量を調節するとゴムの融解により配合材料の造粒時の流動性を改善することができる。又、造粒後ふるいにかけて造粒した粒子の粒子サイズをそろえてもよい。 The premix used in the present invention can be granulated by a conventional method, cured by heat treatment and granulated, and granulated particles using a normal granulator such as a compression mold, a mixing mold, an extrusion mold, etc. Can be When the amount of rubber is adjusted during granulation, fluidity during granulation of the compounding material can be improved by melting the rubber. Moreover, the particle size of the granulated particles may be made uniform by sieving after granulation.
本発明で使用される摩擦材原料は、通常用いられる基材としての繊維成分、結合材、摩擦調整材等であり、非アスベスト系の原料である。
摩擦材の基材である繊維成分としては、スチール繊維、銅繊維、真鍮繊維等の金属繊維;芳香族ポリアミド繊維(アラミドパルプ等:市販品ではデュポン社製、商品名ケブラー等がある)、アクリル繊維、セルロース繊維、耐炎化アクリル繊維等の有機繊維;チタン酸カリウム繊維、ガラス繊維、アルミナ繊維、炭素繊維、ロックウール等の非アスベスト系無機繊維等が挙げられる。これらのうち一種または二種以上を組み合わせて使用することができる。
The friction material raw material used in the present invention is a fiber component, a binder, a friction modifier, or the like as a base material that is usually used, and is a non-asbestos raw material.
The fiber component that is the base material of the friction material includes metal fibers such as steel fibers, copper fibers, and brass fibers; aromatic polyamide fibers (aramid pulp, etc .: commercially available products such as DuPont's brand name Kevlar), acrylic Examples thereof include organic fibers such as fibers, cellulose fibers, and flame-resistant acrylic fibers; non-asbestos inorganic fibers such as potassium titanate fibers, glass fibers, alumina fibers, carbon fibers, and rock wool. One or a combination of two or more of these can be used.
結合材としては、例えば、フェノール樹脂、尿素樹脂、メラミン樹脂、またはそれらの変性樹脂等の熱硬化性樹脂等が挙げられる。
摩擦調整材としては、例えば、カシューダスト、ゴムダスト、メラミンダスト等の有機ダスト;炭酸カルシウム、硫酸バリウム、水酸化カルシウム等のフィラー(充填材);マグネシア、アルミナ、ジルコニア等の金属酸化物等の研削材;アルミニウム粉、銅粉、亜鉛粉等の金属粉、黒鉛、二硫化モリブデン等の潤滑材;等が挙げられ、これらの中から選んだ一種又は適宜組み合わせた二種以上を充填材として使用することができる。
Examples of the binder include thermosetting resins such as phenol resins, urea resins, melamine resins, or modified resins thereof.
Examples of friction modifiers include organic dust such as cashew dust, rubber dust, and melamine dust; fillers such as calcium carbonate, barium sulfate, and calcium hydroxide; grinding of metal oxides such as magnesia, alumina, and zirconia Materials: Metal powders such as aluminum powder, copper powder and zinc powder, lubricants such as graphite and molybdenum disulfide, etc. are used, and one or a combination of two or more selected from these is used as a filler. be able to.
更に、本発明の摩擦材においてロースチール系摩擦材の配合成分はフェノール樹脂、スチール繊維、アラミド繊維、セルロース繊維、炭酸カルシウム、硫酸バリウム、雲母、金属粉、硫化物、黒鉛、有機ダスト、アルミナ、マグネシア、鉱物、酸化鉄等からなる。 Further, in the friction material of the present invention, the components of the low steel friction material are phenol resin, steel fiber, aramid fiber, cellulose fiber, calcium carbonate, barium sulfate, mica, metal powder, sulfide, graphite, organic dust, alumina, It consists of magnesia, minerals, iron oxide, etc.
本発明によるノンアスベスト摩擦材の製造工程の概略はすでに述べたが、従来法と同様に板金プレスにより所定の形状に形成され、脱脂処理及びプライマー処理が施され、そして、接着剤が塗布されたプレッシャプレートと、耐熱性有機繊維や金属繊維等の補強繊維と、無機・有機充填材、摩擦調整材及び熱硬化性樹脂結合材等の粉末原料とを配合し、攪拌により十分に均質化した原材料を常温にて所定の圧力で成形(予備成形)して作成した予備成形体とを、熱成形工程において所定の温度及び圧力で熱成形、又は、予備成形工程を省略し熱成形型に攪拌材料を直接投入し熱成形して両部材を一体に固着し、アフタキュアを行い、最終的に仕上げ処理を施す。 Although the outline of the manufacturing process of the non-asbestos friction material according to the present invention has already been described, it was formed into a predetermined shape by a sheet metal press as in the conventional method, subjected to degreasing treatment and primer treatment, and an adhesive was applied. A raw material that is sufficiently homogenized by stirring by mixing a pressure plate, reinforcing fibers such as heat-resistant organic fibers and metal fibers, and powder materials such as inorganic and organic fillers, friction modifiers, and thermosetting resin binders. A preform formed by molding (preliminary molding) at room temperature at a predetermined pressure is thermoformed at a predetermined temperature and pressure in the thermoforming process, or the preforming process is omitted and the agitating material is added to the thermoforming mold. Is directly injected and thermoformed to fix both members together, after-curing, and finally finishing.
本発明の摩擦材の製造工程において、有効摩耗代とプレミックス含有部分とからなる摩擦材の形成は、一般的な製法で行うことが出来る。すなわち、摩擦材成分に所定量のプレミックスを配合して撹拌した原料と、摩擦材成分だけを撹拌した原料を用意して、所定の厚みになるようにそれぞれ必要量を金型に積層して予備成形する通常の接着層を有する摩擦材と同じ製法を採用できる。 In the manufacturing process of the friction material of the present invention, formation of the friction material comprising the effective wear allowance and the premix-containing portion can be performed by a general manufacturing method. In other words, prepare a raw material with a predetermined amount of premix mixed in the friction material component and agitate, and a raw material with only the friction material component agitated. The same manufacturing method as a friction material having a normal adhesive layer to be preformed can be employed.
以下、実施例を挙げて本発明をさらに詳細に説明するが、本発明の範囲はこれらの実施例により限定されるものではない。 EXAMPLES Hereinafter, although an Example is given and this invention is demonstrated further in detail, the scope of the present invention is not limited by these Examples.
(実施例1〜4、参考例1〜2及び比較例1〜2)
第1表には本発明のプレミックス含有部分に使用した9種類のプレミックスの配合処方を示す。具体的には、クロロブチルゴム、シリコンゴム、NBRゴム、スチール繊維、アラミド繊維、セルロース繊維、フィラー及び加硫促進剤の配合比率をそれぞれ変更し、ニーダーで加熱攪拌し、平均粒径が約0.5〜4mmの不定形粒子に造粒熱処理した。
(Examples 1-4, Reference Examples 1-2 and Comparative Examples 1-2)
Table 1 shows the formulation of nine types of premixes used in the premix-containing part of the present invention. Specifically, the blending ratios of chlorobutyl rubber, silicon rubber, NBR rubber, steel fiber, aramid fiber, cellulose fiber, filler and vulcanization accelerator are changed, and the mixture is heated and stirred with a kneader, and the average particle size is about 0.00. A granulated heat treatment was performed on 5 to 4 mm irregular shaped particles.
(ブレーキパッドの作成)
第2表記載の処方に従って、調製した混合物を常温、20MPaで1分間加圧して予備成形した。次に、プライマー処理を施しフェノール樹脂系接着剤を塗布したプレシャープレートと共に熱成形金型内に、プレミックス含有配合物、有効摩擦代となる摩擦材の配合物を順次セットし、20〜80MPa、100〜170℃の温度で1〜10分間熱成形した。そして、200〜400℃で20〜200分間熱処理を行い、ブレーキパッドを作成した。その際、本発明のプレミックス含有部分の厚みは1mmと2mmである。
第2表には、本発明のプレミックスを含む摩擦材の配合処方と摩擦材の試験結果を示す。摩擦材はロースチール系摩擦材であり、各種配合材料の配合比率は下記の通りである。 参考例1〜2及び実施例1〜3の摩擦材にはプレミックス配合例3を使用し、実施例4にはプレミックス配合例9を使用した。比較例1は、図2に示すようにプレミックスを添加しない標準型の摩擦材であり、比較例2は、図3に示す如く摩擦材中にプレミックスを均一に添加したものである。
(Create brake pads)
According to the formulation shown in Table 2, the prepared mixture was preliminarily molded by pressing at room temperature and 20 MPa for 1 minute. Next, a premix-containing compound and a friction material compound serving as an effective friction allowance are sequentially set in a thermoforming mold together with a pressure plate subjected to primer treatment and coated with a phenol resin adhesive, and 20-80 MPa, Thermoformed at a temperature of 100 to 170 ° C. for 1 to 10 minutes. And heat processing was performed at 200-400 degreeC for 20-200 minutes, and the brake pad was created. In that case, the thickness of the premix containing part of this invention is 1 mm and 2 mm.
Table 2 shows the formulation of the friction material containing the premix of the present invention and the test results of the friction material. The friction material is a low steel friction material, and the blending ratio of various blending materials is as follows. For the friction materials of Reference Examples 1-2 and Examples 1-3 , Premix Formulation Example 3 was used, and for Example 4 , Premix Formulation Example 9 was used. Comparative Example 1 is a standard friction material to which no premix is added as shown in FIG. 2, and Comparative Example 2 is a friction material in which a premix is uniformly added as shown in FIG.
ロースチール系摩擦材(実施例)の配合比率(vol%)
フェノール樹脂:20
炭酸カルシウム:10
硫酸バリウム :10
カシューダスト: 5
黒鉛 :20
アルミナ : 5
アラミド繊維 : 5
スチール繊維 :20
銅 : 5
Mixing ratio of low steel friction material (Example) (vol%)
Phenolic resin: 20
Calcium carbonate: 10
Barium sulfate: 10
Cashew dust: 5
Graphite: 20
Alumina: 5
Aramid fiber: 5
Steel fiber: 20
Copper: 5
(摩擦材の評価)
作成した8種のブレーキパッドの摩擦性能及び物性値を測定した。その測定結果を第2表に示す。第2表中、異音はノイズ試験による異音の有無を評価し、鳴き特性は実車試験で行い、下記評価基準で判定した。
×:悪い
△:目標ぎりぎり
○:良好
摩擦係数はJASO C406に準拠し計測した。又、剪断強度はJASO C427に従い、20℃における強度を測定した。圧縮変形はAK−Standard(液圧100bar相当時の変位量)に従い測定した。
上記の評価結果から、せん断強度・圧縮変形・摩擦特性のバランスから接着面付近のプレミックス部分のプレミックス配合量は配合基材全体に対し20〜40vol%が適当である。
(Evaluation of friction material)
The friction performance and physical property values of the 8 types of brake pads prepared were measured. The measurement results are shown in Table 2. In Table 2, abnormal noise was evaluated for the presence or absence of abnormal noise by a noise test.
X: Bad Δ: Near the target ○: Good The friction coefficient was measured according to JASO C406. The shear strength was measured according to JASO C427 at 20 ° C. The compressive deformation was measured according to AK-Standard (displacement amount corresponding to a hydraulic pressure of 100 bar).
From the above evaluation results, the premix compounding amount in the premix part in the vicinity of the adhesive surface is appropriately 20 to 40 vol% based on the balance of shear strength, compression deformation and friction characteristics.
本発明により、鳴き、異音の発生が抑えられ、フェード特性と耐摩耗性が両立した摩擦部材が実用化された。従って、本発明の摩擦材は、産業機械、鉄道車両、荷物車両、乗用車などに使用されるブレーキパッド、ブレーキライニング、クラッチフェーシング等に特に有用である。 According to the present invention, a friction member that suppresses the occurrence of squeal and abnormal noise and has both fade characteristics and wear resistance has been put to practical use. Therefore, the friction material of the present invention is particularly useful for brake pads, brake linings, clutch facings and the like used for industrial machines, railway vehicles, luggage vehicles, passenger cars and the like.
1 摩擦部材
2 プレッシャプレート
3 接着面
4 プレミックス
5 有効摩耗代
6 摩擦材
7 プレミックス含有部分
DESCRIPTION OF SYMBOLS 1
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JP2006269294A JP5183902B2 (en) | 2006-09-29 | 2006-09-29 | Non-asbestos friction member |
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EP3916264B1 (en) | 2020-05-19 | 2022-11-30 | TMD Friction Services GmbH | Damping material for a damping or intermediate layer for brake linings and a method for producing the damping material |
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JP5183900B2 (en) * | 2005-11-14 | 2013-04-17 | 曙ブレーキ工業株式会社 | Non-asbestos friction member |
US10948027B2 (en) * | 2019-03-08 | 2021-03-16 | Schaeffler Technologies AG & Co. KG | Wet clutch friction plate |
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JPS57192639A (en) * | 1981-05-21 | 1982-11-26 | Sumitomo Electric Ind Ltd | Friction member |
JPS5821031A (en) * | 1981-07-29 | 1983-02-07 | Hitachi Chem Co Ltd | Disc brake pad |
JPS61162537A (en) * | 1985-01-11 | 1986-07-23 | Toyota Motor Corp | Frictional material composition |
JP3088024B2 (en) * | 1991-04-05 | 2000-09-18 | 日清紡績株式会社 | Non-asbestos friction material |
JP3409426B2 (en) * | 1994-05-02 | 2003-05-26 | 住友電気工業株式会社 | Manufacturing method of disc brake pad |
JPH07292348A (en) * | 1994-04-27 | 1995-11-07 | Aisin Chem Co Ltd | Frictional material |
JP2878120B2 (en) * | 1994-07-01 | 1999-04-05 | アイシン化工株式会社 | Brake pad |
JP3391120B2 (en) * | 1994-11-17 | 2003-03-31 | 住友電気工業株式会社 | Manufacturing method of disc brake pad |
JPH10226783A (en) * | 1997-02-17 | 1998-08-25 | Hitachi Chem Co Ltd | Friction material composition and production of friction material therefrom |
JP4380034B2 (en) * | 1999-07-30 | 2009-12-09 | 日清紡ホールディングス株式会社 | Non-asbestos friction material |
JP5183900B2 (en) * | 2005-11-14 | 2013-04-17 | 曙ブレーキ工業株式会社 | Non-asbestos friction member |
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EP3916264B1 (en) | 2020-05-19 | 2022-11-30 | TMD Friction Services GmbH | Damping material for a damping or intermediate layer for brake linings and a method for producing the damping material |
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