JP2000329674A - Method for testing resin permeability in preliminarily molded body of power and grain - Google Patents

Method for testing resin permeability in preliminarily molded body of power and grain

Info

Publication number
JP2000329674A
JP2000329674A JP11141912A JP14191299A JP2000329674A JP 2000329674 A JP2000329674 A JP 2000329674A JP 11141912 A JP11141912 A JP 11141912A JP 14191299 A JP14191299 A JP 14191299A JP 2000329674 A JP2000329674 A JP 2000329674A
Authority
JP
Japan
Prior art keywords
resin
sample
friction material
mold
molded body
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP11141912A
Other languages
Japanese (ja)
Inventor
Akinobu Hashimoto
顕宣 橋本
Katsuo Arai
勝男 新井
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Akebono Research and Development Centre Ltd
Original Assignee
Akebono Research and Development Centre Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Akebono Research and Development Centre Ltd filed Critical Akebono Research and Development Centre Ltd
Priority to JP11141912A priority Critical patent/JP2000329674A/en
Publication of JP2000329674A publication Critical patent/JP2000329674A/en
Pending legal-status Critical Current

Links

Landscapes

  • Braking Arrangements (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)

Abstract

PROBLEM TO BE SOLVED: To select an optimum material for a molded body by a method wherein the preliminarily molded body of a power and grain is put into a molding mold so as to be heated to a thermal molding temperature, a resin is filled, pressurized and hardened, a molded body sample is taken out from the molding mold so as to be cut and the permeation distance of the resin is measured. SOLUTION: Graphite as a sample 7 is filled into a sample housing chamber 4 in a molding mold 2. Then, the sample 7 is heated by a heating heater 6, and it is heated until it reaches a prescribed temperature. Then, a phenolic resin as a resin 9 in a prescribed amount is filled into the sample housing chamber 4 in the central part, an upper punch 5 is set quickly, a prescribed load is applied from the upper part, and the phenolic resin 9 is permeated into a graphite power layer. After the phenolic resin 9 is pressurized for a prescribed time, the sample 7 is taken out from the molding mold 2 so as to be cut, and a distance at which the phenolic resin 9 is permeated into the sample 7 is measured on the basis of the resin permeated part of the sample 7.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、粉粒物の予備成形
体の樹脂浸透性試験方法、例えば摩擦材の予備成形体の
樹脂浸透性試験方法に関するものであり、技術内容的に
は摩擦材用原料及びその攪拌混合物とバインダーである
熱硬化性樹脂との親和性(相性)を評価する方法に関す
るものであり、特に自動車、鉄道車両、産業機械等のブ
レーキ用摩擦材の結合材樹脂以外の摩擦材原材料及びそ
れらの混合物と摩擦材のバインダーである熱硬化性樹脂
との親和性(濡れ性)、更に摩擦材原材料攪拌混合物中
の耐熱性有機繊維の解繊度合いを評価する試験方法に関
する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for testing the resin permeability of a preformed body of a granular material, for example, a method of testing the resin permeability of a preformed body of a friction material. The present invention relates to a method for evaluating the affinity (compatibility) between a raw material for use and a stirred mixture thereof and a thermosetting resin as a binder, and particularly relates to a method other than a binder resin for a friction material for brakes of automobiles, railway vehicles, industrial machines, and the like. The present invention relates to a test method for evaluating an affinity (wetting property) between a friction material raw material and a mixture thereof and a thermosetting resin as a binder of the friction material, and a degree of fibrillation of heat-resistant organic fibers in the friction material raw material stirring mixture.

【0002】[0002]

【従来の技術】従来、自動車、鉄道車両、産業機械等の
ブレーキ用摩擦材の製造においては、主としてブレーキ
などに用いられる摩擦材は、その配合成分としては、一
般に各種充填材、補強のための各種繊維、研磨材、黒
鉛、金属粉等の摩擦調整剤と共に、これらの材料を結合
するための結合材として各種樹脂が配合されている。従
来知られている摩擦材の製造方法の1例であるディスク
ブレーキ用ディスクパッドの製造工程においては、板金
プレスにより所定の形状に成形され、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、耐熱性有機繊維や無機繊維、金属繊維
等の繊維基材と、無機・有機充填材、摩擦調整材及び熱
硬化性樹脂バインダー(具体的にはフェノール樹脂)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
材料を常温にて圧力で成形(予備成形)して作製した予
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工程からなる。
2. Description of the Related Art Conventionally, in the production of friction materials for brakes of automobiles, railway vehicles, industrial machines, etc., friction materials mainly used for brakes and the like generally contain various kinds of fillers and reinforcing materials as components. Various resins are blended together with various fibers, abrasives, graphite, metal powder, and other friction modifiers as a binder for binding these materials. In a manufacturing process of a disk pad for a disk brake, which is an example of a conventionally known method of manufacturing a friction material, the disk pad is formed into a predetermined shape by a sheet metal press, degreased and primed, and an adhesive is applied. Pressure plate, fibrous base material such as heat-resistant organic fiber, inorganic fiber, and metal fiber, and powder raw materials such as inorganic / organic filler, friction modifier, and thermosetting resin binder (specifically, phenol resin) And a preformed body prepared by molding (preforming) the raw material sufficiently homogenized by stirring at room temperature under pressure (preforming), and thermoforming at a predetermined temperature and pressure in a thermoforming step. Are integrally fixed, after-cured, and finally subjected to a finishing process.

【0003】摩擦材の製造は、上記したように摩擦材材
料の配合、攪拌、予備成形、熱成形、加熱、研磨・溝加
工の仕上げ等の各工程からなるが、その中でも配合、攪
拌の工程における摩擦材原材料とバインダーであるフェ
ノール樹脂との親和性(濡れ性、接触角など)は、成形
体強度に関わる因子として問題とされている。また、原
材料を所定量計量した後に行われる攪拌時に、補強用に
配合されているアラミド繊維の解繊度と樹脂の親和性も
問題とされている。
As described above, the production of a friction material comprises the steps of blending, stirring, preforming, thermoforming, heating, polishing and grooving, etc. of the friction material as described above. The affinity (wetting property, contact angle, etc.) between the friction material raw material and the phenol resin as a binder in the above is considered as a factor relating to the strength of the compact. Further, at the time of agitation performed after measuring a predetermined amount of raw materials, the degree of defibration of the aramid fiber blended for reinforcement and the affinity of the resin are also problematic.

【0004】[0004]

【発明が解決しようとする課題】しかし、これらを直接
評価できる方法はなかった。粉体の濡れ性を測定する毛
細管吸引時間法や、ウィルヘルミ法、粉体層に液体が浸
透していく早さを測定する方法などが一般的に知られて
いるが、これらは加熱することができなく、粘度が高い
液体には適さないため、常温で固体であるフェノール樹
脂との濡れ性の評価には利用できないという問題点があ
った。
However, there is no method for directly evaluating these. The capillary suction time method for measuring the wettability of the powder, the Wilhelmy method, and the method for measuring the speed at which the liquid permeates the powder layer are generally known, but these can be heated. However, it is not suitable for a liquid having a high viscosity and cannot be used for evaluating wettability with a phenol resin which is solid at normal temperature.

【0005】本発明は、このような従来の課題に鑑みて
なされたものであり、本質的には、フェノール樹脂以外
の摩擦材用原材料及びそれらの混合物と摩擦材のバイン
ダーであるフェノール樹脂との親和性(濡れ性)を評価
する樹脂浸透性試験方法であって、摩擦材用原料攪拌混
合物中のアラミド繊維の解繊度合いも評価する試験方法
を提供することを目的とする。
[0005] The present invention has been made in view of such conventional problems, and is essentially composed of a friction material raw material other than a phenol resin and a mixture thereof and a phenol resin which is a binder of the friction material. An object of the present invention is to provide a resin permeability test method for evaluating affinity (wetting), which also evaluates the degree of fibrillation of aramid fibers in a raw material stirring mixture for a friction material.

【0006】本発明は、下記の手段により上記の課題を
解決した。 (1)樹脂により結着する複合材において、成形型内に
粉粒物の予備成形体を入れて熱成形温度に加熱した後、
樹脂を充填し、この樹脂を所定時間加熱加圧した後、加
圧・硬化させた成形体サンプルを成形型から取り出し、
該サンプルを切断し、該サンプル中の樹脂の浸透距離を
測定することを特徴とする粉粒物の予備成形体の樹脂浸
透性試験方法。
The present invention has solved the above problems by the following means. (1) In a composite material to be bound by a resin, after a preform of a granular material is put in a mold and heated to a thermoforming temperature,
After filling the resin and heating and pressurizing the resin for a predetermined time, the pressurized and cured molded body sample is taken out of the mold,
A method for testing the resin permeability of a preform of a granular material, comprising cutting the sample and measuring the penetration distance of the resin in the sample.

【0007】(2)上部に上パンチが嵌通押動可能な開
口部を有し、加熱手段を装備した成形型内に、円筒状の
形態をした摩擦材原材料の予備成形体を縦方向に入れ、
次いで加熱手段により規定温度に達するまで加熱し、そ
の後前記円筒状の予備成形体の中空部に樹脂を所定量充
填し、前記上パンチを前記開口部で荷重を負荷し、所定
時間加熱加圧した後、加圧・硬化させた摩擦材サンプル
を成形型から取り出し、該サンプルを切断し、該サンプ
ル中の樹脂の浸透距離を測定することを特徴とする摩擦
材原材料の樹脂浸透性試験方法。
(2) A cylindrical preform of a friction material raw material is vertically arranged in a forming die having an opening through which an upper punch can be fitted and pushed and provided with a heating means. Get in,
Next, heating was performed by a heating means until a specified temperature was reached, and thereafter, a predetermined amount of resin was filled in the hollow portion of the cylindrical preform, and a load was applied to the upper punch through the opening, and heating and pressing were performed for a predetermined time. Thereafter, a friction material sample that has been pressed and cured is removed from the mold, the sample is cut, and the penetration distance of the resin in the sample is measured.

【0008】[0008]

【発明の実施の形態】本発明では、摩擦材の製造におい
て、摩擦材用原材料の配合、攪拌混合工程中にそこで起
きている摩擦材用原料とバインダーである熱硬化性樹脂
との親和性、及び補強用に配合されている耐熱性有機繊
維の解繊度と樹脂との親和性を正確に測定するために、
常温で固体であるフェノール樹脂等を加熱溶融し、その
工程の摩擦材用原料やそれらの攪拌混合物中への樹脂浸
透性を、加熱溶融後の原料等への浸透距離を測定するこ
とにより評価するものである。また、耐熱性有機繊維の
開繊度と樹脂の親和性も併せて評価するものである。こ
のため、摩擦材用原料やそれらの攪拌混合物中へ樹脂を
浸透させたものは、取り出して測定する必要があるの
で、加熱加圧に用いる成形型は加熱加圧後の溶融した樹
脂が浸透した摩擦材用原料やそれらの攪拌混合物を取り
出し易いような形式のものにすることが必要であり、例
えば、成形型は割り型形式のものが好ましい。
BEST MODE FOR CARRYING OUT THE INVENTION In the present invention, in the production of a friction material, an affinity between a friction material material and a thermosetting resin as a binder, which occurs during the mixing and stirring and mixing steps of the friction material raw material, In order to accurately measure the degree of fibrillation of the heat-resistant organic fiber blended for reinforcement and the affinity with the resin,
Heat-melt phenolic resin, etc., which is solid at normal temperature, and evaluate the resin permeability of the friction material in the process and the stirred mixture thereof by measuring the penetration distance into the material after heating and melting. Things. In addition, the degree of opening of the heat-resistant organic fiber and the affinity of the resin are also evaluated. For this reason, it is necessary to take out and measure the resin infiltrated into the raw material for the friction material and the stirred mixture thereof, so that the molten resin after the heat and pressure permeated the mold used for heating and pressing. It is necessary to use a type in which the raw materials for the friction material and the stirred mixture thereof can be easily taken out. For example, the mold is preferably of a split type.

【0009】本発明で浸透性(親和性)を調べることが
できる熱硬化性樹脂バインダーとしては、フェノール樹
脂(ストレートフェノール樹脂、ゴム等による各種変性
フェノール樹脂を含む)を用いるに適しているが、熱硬
化性の他の樹脂、例えばメラミン樹脂、ポリイミド樹脂
等の場合に適用することができる。また、摩擦材の補強
用に配合される繊維基材として耐熱性有機繊維、金属繊
維や無機繊維が挙げられる。これらの繊維のうち、金属
繊維や無機繊維は、短時間の攪拌、混合工程で比較的容
易に解繊するので特に問題はないが、太さが細い耐熱性
有機繊維が柔軟なこともあって比較的解繊し難く、その
解繊度と樹脂の親和性が摩擦材の強度に影響を及ぼし問
題となる。
As the thermosetting resin binder whose permeability (affinity) can be examined in the present invention, it is suitable to use a phenol resin (including various modified phenol resins such as straight phenol resin and rubber). The present invention can be applied to other thermosetting resins such as a melamine resin and a polyimide resin. In addition, examples of the fiber base compounded for reinforcing the friction material include heat-resistant organic fibers, metal fibers, and inorganic fibers. Among these fibers, metal fibers and inorganic fibers are not particularly problematic because they can be defibrated relatively easily in a short stirring and mixing process, but the heat-resistant organic fibers having a small thickness may be flexible. It is relatively difficult to defibrate, and the degree of defibration and the affinity of the resin affect the strength of the friction material, which is a problem.

【0010】耐熱性有機繊維としては、芳香族ポリアミ
ド繊維(アラミド繊維、アラミドパルプ)、耐炎性アク
リル繊維等が好ましく用いることができる。なかでも、
強度が大でかつ耐熱性が大であるという利点からアラミ
ド繊維を好ましく使用することができる。好適なアラミ
ド繊維の市販品としては、デュポン社製のケブラー(K
evlar)29、ケブラー(Kevlar)49、ケ
ブラー(Kevlar)149を挙げることができる。
なお、ケブラー(Kevlar)は商品名である。上記
した事象を考慮して、本発明では、バインダーとしてフ
ェノール樹脂を、補強用繊維基材としてアラミド繊維を
選んで浸透性(親和性)の実験を行った。
As the heat-resistant organic fibers, aromatic polyamide fibers (aramid fibers, aramid pulp), flame-resistant acrylic fibers and the like can be preferably used. Above all,
Aramid fiber can be preferably used from the advantage of high strength and high heat resistance. Suitable commercial products of aramid fiber include Kevlar (K) manufactured by DuPont.
evlar) 29, Kevlar 49 and Kevlar 149.
Kevlar is a trade name. In view of the above-mentioned events, in the present invention, a phenol resin was selected as a binder and an aramid fiber was selected as a reinforcing fiber base material, and an experiment of permeability (affinity) was performed.

【0011】具体的な試験条件を挙げると、次のとおり
である。前記摩擦材用原材料又はその攪拌混合物の充填
物の見掛け密度が0.6g/cm3 、空隙率が0.73
で、加熱の規定温度が150℃で、固体バインダー充填
物の所定量が摩擦材用原材料又はその攪拌混合物全体の
10重量%で、上パンチに負荷する規定荷重が7.85
トン、面圧400kg/cm2 で、加圧時間が2〜10
分間であることが好ましい。なお、この試験において留
意すべきことは、摩擦材用原材料又はその攪拌混合物に
対して使用するバインダーの量は少なめとして、バイン
ダーが全部に浸透することなく、途中で止まるような条
件とすることが好ましい。これは各試験ともバインダー
が全部に浸透することになると、区別がつかず測定でき
なくなるからである。その条件としては、或いは加圧時
間を加減することもできる。
The specific test conditions are as follows. The packing of the raw material for friction material or the stirred mixture thereof has an apparent density of 0.6 g / cm 3 and a porosity of 0.73.
The specified temperature of heating is 150 ° C., the predetermined amount of the solid binder filler is 10% by weight of the raw material for the friction material or the whole of the stirred mixture, and the specified load applied to the upper punch is 7.85.
Ton, surface pressure 400 kg / cm 2 , pressurization time 2-10
Minutes. In this test, it should be noted that the amount of the binder used for the raw material for the friction material or the stirred mixture thereof should be small, and the conditions should be such that the binder does not penetrate all but stops halfway. preferable. This is because, in each test, if the binder penetrates all, it cannot be distinguished and cannot be measured. As the condition, or alternatively, the pressurizing time can be adjusted.

【0012】[0012]

【実施例】以下、実施例により本発明を具体的に説明す
る。ただし、本発明はこれらの実施のみに限定されるも
のではない。
The present invention will be described below in detail with reference to examples. However, the invention is not limited to only these implementations.

【0013】実施例1 図1に示すように、試験装置1として、上部に上パンチ
5が嵌め入れられて上下動が滑らかに行われる開口部3
を持ち、内部にサンプル収容室4を持つ成形型2を用い
た。この成形型2はその周囲に加熱用の加熱用ヒーター
6を有している。成形型2内部のサンプル収容室4に摩
擦材用原材料やそれらの攪拌混合物を中空円筒状の形に
軽く圧縮することにより予備成形したサンプル7を、そ
の中空円筒の中心軸が垂直になるように配置して入れ
る。この中空円筒状の形状を有するサンプル7の外径は
サンプル収容室4の内径と同じにし、内径は上パンチ5
の外径と同じとする。この試験装置1では、サンプル7
を入れた後、加熱用ヒーター6で加熱した後、サンプル
7の中空部8にバインダーとして樹脂9を入れ、上パン
チ5を加圧してバインダー8を加圧できるように動作さ
れる。この成形型2は、開口部3の口径がサンプル7の
直径より小さいため、予備成形したサンプル7をサンプ
ル収容室4に入れられないし、また加圧・硬化させたサ
ンプル7を成形型2の内部から取り出せないから、容易
に取り出せるように2分割型の金型を使用した。
Embodiment 1 As shown in FIG. 1, as a test apparatus 1, an opening 3 in which an upper punch 5 is fitted into an upper portion and which can be moved up and down smoothly.
And a molding die 2 having a sample storage chamber 4 inside. The mold 2 has a heater 6 for heating around the mold. A sample 7 pre-formed by lightly compressing the raw materials for friction material and their stirring mixture into a hollow cylindrical shape in a sample storage chamber 4 inside the mold 2 so that the central axis of the hollow cylinder becomes vertical. Place and put. The outer diameter of the sample 7 having the hollow cylindrical shape is the same as the inner diameter of the sample storage chamber 4, and the inner diameter is the upper punch 5.
And the same outer diameter as In this test apparatus 1, the sample 7
After the heating, the heater 9 is heated, and then the resin 9 is put into the hollow portion 8 of the sample 7 as a binder, and the upper punch 5 is pressed so that the binder 8 can be pressed. Since the diameter of the opening 3 is smaller than the diameter of the sample 7, the preformed sample 7 cannot be put into the sample accommodating chamber 4, and the sample 7 that has been pressurized and cured is placed inside the molding die 2. Since it cannot be taken out of the mold, a two-part mold was used so that it could be easily taken out.

【0014】樹脂浸透性の試験は、下記の手順によって
行った。 (1)図1に示す成形型2に、サンプル7として、黒鉛
A(A社製、平均粒径35μm)と、黒鉛B(B社製、
平均粒径同じく35μm)を所定の見かけ密度(ここで
は0.6g/cm3 、空間率0.73)になるようにサ
ンプル収容室4に充填した。 (2)成形型2の加熱用ヒーター6により加熱し、サン
プル(黒鉛)7が規定温度(ここでは実際の熱成形温度
に相当する温度の150℃)に達するまで維持する。 (3)中心部分のサンプル収容室4に樹脂9として、フ
ェノール樹脂(ノボラック型フェノール樹脂/ヘキサメ
チレンジアミン(硬化剤))を所定量(ここではサンプ
ルの10重量%)充填し、素早く上パンチ5をセット
し、上部より規定荷重(ここでは7.85ton、面圧
400kg/cm2 )をかけ、黒鉛粉体層10にフェノ
ール樹脂9を浸透させる。 (4)所定時間加圧後(ここでは10分間)、サンプル
7を成形型2から取り出して切断し、サンプル7の樹脂
浸透部分10からサンプル7中に樹脂9が浸透した距離
11を測定する。
The test for resin permeability was conducted according to the following procedure. (1) Graphite A (manufactured by Company A, average particle diameter 35 μm) and graphite B (manufactured by Company B,
An average particle size of 35 μm) was filled in the sample accommodating chamber 4 so as to have a predetermined apparent density (here, 0.6 g / cm 3 , porosity 0.73). (2) Heat by the heating heater 6 of the mold 2 and maintain it until the sample (graphite) 7 reaches a specified temperature (here, 150 ° C., a temperature corresponding to the actual thermoforming temperature). (3) A predetermined amount of phenolic resin (novolak-type phenolic resin / hexamethylenediamine (curing agent)) (here, 10% by weight of the sample) is filled as the resin 9 in the sample accommodating chamber 4 at the center, and the upper punch 5 is quickly filled. Is set, a specified load (7.85 ton, surface pressure: 400 kg / cm 2 in this case ) is applied from above, and the phenol resin 9 is permeated into the graphite powder layer 10. (4) After pressurizing for a predetermined time (here, 10 minutes), the sample 7 is taken out of the mold 2 and cut, and the distance 11 from which the resin 9 has penetrated into the sample 7 from the resin permeated portion 10 of the sample 7 is measured.

【0015】(5)測定結果を第1表に示す。この測定
結果からみて、黒鉛Bよりも黒鉛Aの方がフェノール樹
脂との親和性が良いことが確認された。なお、黒鉛Aは
無定形黒鉛で、黒鉛Bは結晶性黒鉛である。
(5) Table 1 shows the measurement results. From the measurement results, it was confirmed that graphite A had better affinity with the phenol resin than graphite B. Graphite A is amorphous graphite, and graphite B is crystalline graphite.

【0016】[0016]

【表1】 [Table 1]

【0017】実施例2 実施例1の前記(1)の黒鉛の代わりに、下記第2表に
示す配合割合の摩擦材用原材料(フェノール樹脂は含ま
れていない)の攪拌時間2分間の攪拌混合物(C)と、
6分間の混合物(D)を使用した以外は実施例1と同様
の試験手順を繰り返した。測定結果を下記第3表に示
す。第3表に示す測定結果から、攪拌時間が長い方が補
強用アラミド繊維がいっそう十分に解繊され、その結果
摩擦材用原料混合物とフェノール樹脂の親和性(濡れ
性)が向上し、摩擦材の強度も向上することが推測され
る。
Example 2 Instead of the graphite of the above (1) of Example 1, a mixture of the raw materials for a friction material (containing no phenol resin) in the mixing ratio shown in the following Table 2 was stirred for 2 minutes. (C),
The same test procedure as in Example 1 was repeated, except that the mixture (D) for 6 minutes was used. The measurement results are shown in Table 3 below. From the measurement results shown in Table 3, the longer the stirring time, the more sufficiently the reinforcing aramid fiber was defibrated, and as a result, the affinity (wetting property) between the raw material mixture for friction material and the phenol resin was improved, and the friction material was improved. It is presumed that the strength of the steel is also improved.

【0018】[0018]

【表2】 [Table 2]

【0019】[0019]

【表3】 [Table 3]

【0020】[0020]

【発明の効果】本発明によれば、加熱及び加圧が可能
で、加熱・硬化させた摩擦材サンプルを容易に取り出せ
る成形型を使用することによって、従来の方法では不可
能であった摩擦材用原材料及びそれらの攪拌混合物と樹
脂の親和性が測定できるようになった結果、最適な成形
体を得るための材料の選択が容易となった。また、ブレ
ーキパッド成形体の物性に影響する摩擦材用原材料の攪
拌混合物の攪拌度(特にアラミド繊維の解繊度)を測定
し、規定することもできるようになった。
According to the present invention, by using a mold which can be heated and pressurized and can easily take out a heated and cured friction material sample, the friction material which cannot be obtained by the conventional method can be obtained. As a result of being able to measure the affinity between the raw materials and the stirred mixture thereof and the resin, it became easy to select the material for obtaining the optimum molded product. In addition, the degree of agitation of the agitated mixture of the raw materials for the friction material which affects the physical properties of the molded brake pad (particularly, the degree of fibrillation of aramid fibers) can be measured and specified.

【図面の簡単な説明】[Brief description of the drawings]

【図1】本発明の樹脂浸透性試験方法に使用する試験装
置の断面図を示す。
FIG. 1 is a cross-sectional view of a test apparatus used for a resin permeability test method of the present invention.

【図2】本発明の樹脂浸透性試験方法に使用する試験装
置の平面図を示す。
FIG. 2 shows a plan view of a test apparatus used for the resin permeability test method of the present invention.

【図3】浸透試験結果を示す断面図である。FIG. 3 is a sectional view showing the results of a penetration test.

【符号の説明】[Explanation of symbols]

1 試験装置 2 成形型 3 開口部 4 サンプル収容室 5 上パンチ 6 加熱用ヒーター 7 サンプル(黒鉛又は攪拌混合物) 8 中空部 9 樹脂 10 樹脂浸透部分 11 浸透距離 DESCRIPTION OF SYMBOLS 1 Test apparatus 2 Mold 3 Opening 4 Sample accommodating chamber 5 Upper punch 6 Heater 7 Sample (graphite or stirring mixture) 8 Hollow part 9 Resin 10 Resin penetration part 11 Penetration distance

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 樹脂により結着する複合材において、成
形型内に粉粒物の予備成形体を入れて熱成形温度に加熱
した後、樹脂を充填し、この樹脂を所定時間加熱加圧し
た後、加圧・硬化させた成形体サンプルを成形型から取
り出し、該サンプルを切断し、該サンプル中の樹脂の浸
透距離を測定することを特徴とする粉粒物の予備成形体
の樹脂浸透性試験方法。
In a composite material bound by a resin, a preform of a granular material is put into a mold, heated to a thermoforming temperature, filled with a resin, and heated and pressed for a predetermined time. Thereafter, the pressed and cured molded product sample is taken out of the mold, the sample is cut, and the penetration distance of the resin in the sample is measured. Test method.
【請求項2】 上部に上パンチが嵌通押動可能な開口部
を有し、加熱手段を装備した成形型内に、円筒状の形態
をした摩擦材原材料の予備成形体を縦方向に入れ、次い
で加熱手段により規定温度に達するまで加熱し、その後
前記円筒状の予備成形体の中空部に樹脂を所定量充填
し、前記上パンチを前記開口部で荷重を負荷し、所定時
間加熱加圧した後、加圧・硬化させた摩擦材サンプルを
成形型から取り出し、該サンプルを切断し、該サンプル
中の樹脂の浸透距離を測定することを特徴とする摩擦材
原材料の樹脂浸透性試験方法。
2. A cylindrical preform of a friction material raw material is vertically placed in a forming die having an opening through which an upper punch can be inserted and pushed and provided with a heating means. Then, heating is performed by a heating means until a predetermined temperature is reached, and thereafter, a predetermined amount of resin is filled in the hollow portion of the cylindrical preform, and a load is applied to the upper punch through the opening, and heating and pressing are performed for a predetermined time. A method for testing the permeability of a friction material material to a resin, comprising taking out a pressed and cured friction material sample from a mold, cutting the sample, and measuring a penetration distance of a resin in the sample.
JP11141912A 1999-05-21 1999-05-21 Method for testing resin permeability in preliminarily molded body of power and grain Pending JP2000329674A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11141912A JP2000329674A (en) 1999-05-21 1999-05-21 Method for testing resin permeability in preliminarily molded body of power and grain

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11141912A JP2000329674A (en) 1999-05-21 1999-05-21 Method for testing resin permeability in preliminarily molded body of power and grain

Publications (1)

Publication Number Publication Date
JP2000329674A true JP2000329674A (en) 2000-11-30

Family

ID=15303065

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11141912A Pending JP2000329674A (en) 1999-05-21 1999-05-21 Method for testing resin permeability in preliminarily molded body of power and grain

Country Status (1)

Country Link
JP (1) JP2000329674A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103528934A (en) * 2013-10-29 2014-01-22 中国石油大学(北京) Mutual correlation technology for measuring permeability stress sensitivity of ultra-low permeability rocks
CN103645129A (en) * 2013-12-30 2014-03-19 中国科学院武汉岩土力学研究所 High-temperature ultralow permeability measuring instrument
CN103715846A (en) * 2013-12-31 2014-04-09 嘉兴荣泰雷帕司绝缘材料有限公司 Method and device for representing impregnating capacity between impregnating resin and enameled wire winding

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103528934A (en) * 2013-10-29 2014-01-22 中国石油大学(北京) Mutual correlation technology for measuring permeability stress sensitivity of ultra-low permeability rocks
CN103645129A (en) * 2013-12-30 2014-03-19 中国科学院武汉岩土力学研究所 High-temperature ultralow permeability measuring instrument
CN103715846A (en) * 2013-12-31 2014-04-09 嘉兴荣泰雷帕司绝缘材料有限公司 Method and device for representing impregnating capacity between impregnating resin and enameled wire winding
CN103715846B (en) * 2013-12-31 2016-03-09 嘉兴荣泰雷帕司绝缘材料有限公司 Characterize the method and apparatus of wetting capacity between impregnating resin and enamelled wire winding

Similar Documents

Publication Publication Date Title
JP3778373B2 (en) Improved friction material
EP0074838B1 (en) Aramid containing friction materials and method of producing the same
EP0154488B1 (en) Friction materials and their manufacture
CA2366584C (en) Composite comprising structural and non structural fibers
US9855639B2 (en) Abrasive article
PL169609B1 (en) Method of and apparatus for making composite material products
JP2000329674A (en) Method for testing resin permeability in preliminarily molded body of power and grain
CN109906261B (en) Friction material composition and friction material
Gortner et al. Influence of textile reinforcement on bending properties and impact strength of SMC-components
JP6497088B2 (en) Manufacturing method of back plate, back plate and brake pad
JP2017210616A (en) Fiber-containing resin structure, manufacturing method of fiber-containing resin structure, fiber-reinforced resin cured product and fiber-reinforced resin mold
CN104786575B (en) A kind of asbestos base lamilate, its manufacturing method and its application
Brody et al. The effects of a thermoplastic polyester preform binder on vinyl ester resin
US6558595B1 (en) Method for producing virtually finished moulded bodies from moulding materials
US3003980A (en) Epoxy base friction material and method of making same
Gortner et al. Advanced SMC-Processing in Combination with Textile Reinforcements
Lambla et al. Optimization of phenolic resins for friction materials
JP3800784B2 (en) Manufacturing method of thermosetting resin moldings
Nandiyanto et al. Production of brake pad from epoxy resin: From polymerization concept to the experiment with analysis of mechanical properties
JPS5891935A (en) Manufacture of brake plastic material
CN115972625A (en) Preparation method of carbon fiber composite material for automobile parts
JP2022165655A (en) Method for manufacturing molding material for resin gear, and method for manufacturing resin gear
JP2022164242A (en) Method for manufacturing resin gear and resin gear
JP5720209B2 (en) Manufacturing method of functional parts
JPS5877939A (en) Wet type friction material