JPS5945006B2 - sliding friction material - Google Patents

sliding friction material

Info

Publication number
JPS5945006B2
JPS5945006B2 JP1224777A JP1224777A JPS5945006B2 JP S5945006 B2 JPS5945006 B2 JP S5945006B2 JP 1224777 A JP1224777 A JP 1224777A JP 1224777 A JP1224777 A JP 1224777A JP S5945006 B2 JPS5945006 B2 JP S5945006B2
Authority
JP
Japan
Prior art keywords
resin
friction material
sample
sliding friction
heat
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.)
Expired
Application number
JP1224777A
Other languages
Japanese (ja)
Other versions
JPS5397075A (en
Inventor
辰彦 福岡
靖久 田中
正己 高木
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.)
Taiho Kogyo Co Ltd
Original Assignee
Taiho Kogyo Co 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 Taiho Kogyo Co Ltd filed Critical Taiho Kogyo Co Ltd
Priority to JP1224777A priority Critical patent/JPS5945006B2/en
Publication of JPS5397075A publication Critical patent/JPS5397075A/en
Publication of JPS5945006B2 publication Critical patent/JPS5945006B2/en
Expired legal-status Critical Current

Links

Description

【発明の詳細な説明】 本発明は、耐摩耗性、耐腐蝕性等に優れたすベリ摩擦材
料に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a smooth friction material having excellent wear resistance, corrosion resistance, etc.

すベリ摩擦材料のうちすベリ面に合成樹脂を用いたもの
としては、従来裏金鋼板上に合成樹脂をコーティングし
、これを乾燥、焼成したもの、裏金鋼板上に銅または銅
合金等の金属粉末を焼結し、その焼結多孔質層に合成樹
脂を含浸したもの、あるいは合成樹脂単体(ソリッド)
を直接すベリ摩擦材料として用いるものが一般に知られ
ている。
Conventional sliding friction materials that use synthetic resin on the bottom side include those that coat a steel backing plate with synthetic resin, dry and sinter it, and those that coat a steel backing plate with metal powder such as copper or copper alloy. sintered and the sintered porous layer is impregnated with synthetic resin, or synthetic resin alone (solid)
It is generally known to use directly as a friction material.

しかるにこれらの摩擦材料のうち裏金を用いた上記第一
、第二の材料は1 相対的に摺動し、または当接する二
部材間の電気的絶縁を保持することが困難なため、軸と
軸受、軸受と・・ウジング等の間に電気的絶縁機能を付
与する必要がある場合には使用できない。
However, among these friction materials, the above-mentioned first and second materials that use backing metals are difficult to maintain electrical insulation between two members that slide relative to each other or are in contact with each other. , cannot be used when it is necessary to provide electrical insulation function between the bearing and the housing, etc.

2 裏金の金属が腐蝕するような腐蝕性雰囲気では使用
できない。
2. Cannot be used in a corrosive atmosphere where the metal backing will corrode.

3 軸受に用い、この軸受が強磁性下で使用される場合
には、軸受にうず電流が発生してみかけの摩擦力が高く
なつてしまい、また磁界により摺動面へ鉄粉などの摩耗
粉が付着する結果アブレシブ摩耗が生じるおそれがある
3 When used in a bearing and the bearing is used in a ferromagnetic environment, eddy currents are generated in the bearing, increasing the apparent frictional force, and the magnetic field causes wear particles such as iron powder to be transferred to the sliding surface. As a result of adhesion, abrasive wear may occur.

4 重量が大になる。4. Weight increases.

等の欠点があるため、絶縁性、耐蝕性を要求されるすベ
リ摩擦材料、または強磁界下で使用されるすベリ摩擦材
料としては、裏金鋼板を有するすベー摩擦材料を使用す
ることはできない。
Due to these drawbacks, it is not possible to use a flat friction material with a steel backing plate as a flat friction material that requires insulation and corrosion resistance, or as a flat friction material that is used under a strong magnetic field. .

他方、合成樹脂単体からなる材料は、上記絶縁性、耐蝕
性には問題はないが、一般的に裏金鋼板を用いる材料に
比して耐荷重性が低いため、すベリ摩擦材料として用い
るにはある程度の板厚を必要とするからコストが高くな
り、かつ初期なじみが悪いという欠点がある。本発明は
、上記の事情に鑑み、裏金を有する合成樹脂すベリ摩擦
材料の上記欠点、すなわち耐絶縁性、耐腐蝕性に劣る点
、強磁界下の使用が困難である点、重量が大となる点等
の欠点を解消しかつ合成樹脂単体からなるすベリ摩擦材
料の欠点である初期なじみの悪さ、耐荷重性の低さを改
良することを目的としたものであつて、基材としてガラ
ス繊維またはカーボン繊維をポリイミド樹脂、エポキシ
樹脂等の接着性樹脂に含浸させた耐熱強化プラスチツク
を用いることにより耐荷重性を向上させると共に、上記
基材の表面になじみ性、すベリ特性の良好な合成樹脂混
合物をコーテイングすることにより上記諸欠点を解消し
たものである。
On the other hand, materials made of synthetic resin alone have no problems with the above-mentioned insulation properties and corrosion resistance, but they generally have lower load resistance than materials that use backing steel plates, so they cannot be used as sliding friction materials. The disadvantage is that the cost is high because it requires a certain thickness, and the initial fit is poor. In view of the above circumstances, the present invention addresses the above-mentioned drawbacks of synthetic resin sliding friction materials having a backing metal, namely, poor insulation resistance and corrosion resistance, difficulty in use under strong magnetic fields, and large weight. The purpose of this product is to eliminate the shortcomings such as friction materials that are made of synthetic resin alone, and to improve the shortcomings of poor initial fitting and low load-bearing properties, which are the shortcomings of smooth friction materials made of a single synthetic resin. By using a heat-resistant reinforced plastic in which fibers or carbon fibers are impregnated with an adhesive resin such as polyimide resin or epoxy resin, the load-bearing capacity is improved, and the material has good conformability and smoothness to the surface of the base material. The above-mentioned drawbacks are solved by coating with a resin mixture.

本発明に係るすベリ摩擦材料は、耐熱強化プラスチツク
上に、重量%で10〜35%の接着性樹脂と5〜30%
の芳香族ポリエステル樹脂および残部が4弗化エチレン
樹脂からなる混合物、または上記割合の接着性樹脂と芳
香族ポリエステル樹脂を含んだ混合物にさらに1〜15
%の一種または二種以上の固体潤滑剤を添加して残部を
4弗化エチレン樹脂とした混合物をコーテイングし、乾
燥、焼成したことを特徴とするものである。接着性樹脂
としては、ポリアミドイミド樹脂、ポリイミド樹脂等が
好ましく、これを用いる理由は耐熱強化プラスチツクと
の密着、接着を強化するためである。これの添加量が3
5%を越えると4弗化エチレン樹脂成分が相対的に少な
くなつて4弗化エチレン樹脂の優れた低摩擦性が充分に
発揮されず、また10%を下まわると耐熱強化プラスチ
ツクとの密着力が低下する。次に芳香族ポリエステル樹
脂は、耐熱性、耐摩耗性を向上させ、かつ芳香族ポリエ
ステル樹脂自体の低摩擦性を利用するために添加したも
のであつて、その添加量は5〜35%が好ましい。
The slip-on friction material according to the present invention is made of adhesive resin of 10 to 35% by weight and 5 to 30% of adhesive resin on heat-resistant reinforced plastic.
of an aromatic polyester resin and the remainder is a tetrafluoroethylene resin, or a mixture containing an adhesive resin and an aromatic polyester resin in the above proportions, and further contains 1 to 15% of the aromatic polyester resin.
% of one or more solid lubricants and the remainder is tetrafluoroethylene resin, which is then coated, dried, and fired. As the adhesive resin, polyamide-imide resin, polyimide resin, etc. are preferable, and the reason for using this is to strengthen the adhesion and adhesion with the heat-resistant reinforced plastic. The amount of this added is 3
If it exceeds 5%, the tetrafluoroethylene resin component will be relatively small and the excellent low friction properties of the tetrafluoroethylene resin will not be fully exhibited, and if it is less than 10%, the adhesion with heat-resistant reinforced plastics will decrease. decreases. Next, the aromatic polyester resin is added to improve heat resistance and abrasion resistance, and to take advantage of the low friction properties of the aromatic polyester resin itself, and the amount added is preferably 5 to 35%. .

その理由は、添加量が35%を越えると4弗化エチレン
樹脂成分が少なくなつてその優れた低摩擦性が充分に発
揮されず、逆に5%を下まわると芳香族ポリエステル樹
脂の優れた耐摩耗性等が発揮できないからである。また
、固体潤滑剤は4弗化エチレン樹脂と芳香族ポリエステ
ル樹脂との相乗効果をより顕著にするために加えたもの
である。
The reason for this is that when the amount added exceeds 35%, the amount of the tetrafluoroethylene resin component decreases and its excellent low friction properties cannot be fully demonstrated, while when the amount is less than 5%, the excellent low friction properties of the aromatic polyester resin are reduced. This is because wear resistance etc. cannot be exhibited. Further, the solid lubricant was added to make the synergistic effect between the tetrafluoroethylene resin and the aromatic polyester resin more pronounced.

つまり二硫化モリブデン(MOS2)、鉛(Pb)、グ
ラフアイト(Gr)等の固体潤滑剤は、それ自体低摩擦
性を有しており、これを加えることによつてなじみ性や
親油性をより向上させることができるのである。添加量
は、1%を下まわると添加効果が期待できず、15%を
越えるとコーテイング被膜が胞弱になるので、1〜15
%が望ましい。またこの固体潤滑剤は一種のみならず、
二種以上を混合して用いることができる。なお、残部、
すなわち主成分に4弗化エチレン樹脂を用いたのは前述
のようにこの樹脂の低摩擦性を利用するためである。
In other words, solid lubricants such as molybdenum disulfide (MOS2), lead (Pb), and graphite (Gr) themselves have low friction properties, and by adding them, they can improve compatibility and lipophilicity. It can be improved. If the amount added is less than 1%, no effect can be expected, and if it exceeds 15%, the coating film will become weak, so it should be 1 to 15%.
% is desirable. In addition, this solid lubricant is not only one type,
A mixture of two or more types can be used. In addition, the remainder,
That is, the reason why tetrafluoroethylene resin is used as the main component is to take advantage of the low friction properties of this resin as described above.

本発明のすベリ摩擦材料は、以上のように耐熱強化プラ
スチツクに上記組成の混合物をコーテイングし、これを
乾燥、焼成することにより得られるものであるが、上記
コーテイングの前工程において、耐熱強化プラスチツク
に、接着性樹脂と4弗化エチレン樹脂との混合物によつ
て下塗を施すことにより、コーテイングした樹脂と耐熱
強化プラスチツクとのより強い密着が得られ、また、コ
ーテイングした樹脂表面にオイルポケツトを設ければ、
極めて低摩擦で給油メンテナンスの不要なすベリ摩擦材
料が得られる。
The sliding friction material of the present invention is obtained by coating a heat-resistant reinforced plastic with a mixture having the above composition, drying and firing it as described above. By applying an undercoat with a mixture of adhesive resin and tetrafluoroethylene resin, stronger adhesion between the coated resin and the heat-resistant reinforced plastic can be obtained, and oil pockets can also be provided on the coated resin surface. If so,
A very friction material with extremely low friction and no need for lubrication and maintenance can be obtained.

なお、上記下塗を施す場合に11ζその膜厚を0.00
5〜0.010鰭程度とすることが望ましい。次に、実
施例にしたがつて本発明を説明する。
In addition, when applying the above-mentioned undercoat, the film thickness of 11ζ is 0.00
It is desirable to set it to about 5 to 0.010 fins. Next, the present invention will be explained based on examples.

実施例 1(試料7f6.1、2、3)ガラス繊維また
はカーボン繊維にポリイミド樹脂を含浸したシート材(
以下、耐熱強化プラスチツクという)をサンデイング処
理し、水洗後90〜100℃で30分間乾燥して水分を
除く。
Example 1 (Samples 7f6.1, 2, 3) Sheet material made of glass fiber or carbon fiber impregnated with polyimide resin (
The plastic (hereinafter referred to as heat-resistant reinforced plastic) is sanded, washed with water, and then dried at 90 to 100° C. for 30 minutes to remove moisture.

次に、ポリアミドイミド樹脂(第1表中にPAIと略記
)、芳香族ポリエステル樹脂および4弗化エチレン樹脂
(残部、第1表中に4Fと略記)とを第1表に示す割合
で混合し、これを耐熱強化プラスチツク上にスプレーコ
ーテイングしたのち、90〜100℃で30分間乾燥し
て溶剤を蒸発させ、さらに、280℃で30分間焼成し
てすべり摩擦材料とした。実施例 2(試料7V).4
、5、6) 耐熱強化プラスチツクをサンデイング処理し、水洗後9
0〜100℃で30分間乾燥して水分を除く。
Next, polyamide-imide resin (abbreviated as PAI in Table 1), aromatic polyester resin, and tetrafluoroethylene resin (remainder, abbreviated as 4F in Table 1) were mixed in the proportions shown in Table 1. This was spray coated onto a heat-resistant reinforced plastic, dried at 90 to 100°C for 30 minutes to evaporate the solvent, and further baked at 280°C for 30 minutes to obtain a sliding friction material. Example 2 (sample 7V). 4
, 5, 6) After sanding the heat-resistant reinforced plastic and washing with water,
Dry at 0 to 100°C for 30 minutes to remove moisture.

次に下塗としてポリアミドイミド樹脂(第1表中にPA
Iと略記)と4弗化エチレン樹脂(同4Fと略記)との
第1表に示す割合の混合物をスプレーコーテイングし、
90〜100℃で30分間乾燥する。この下塗の終了し
た耐熱強化プラスチツクに、ポリアミドイミド樹脂、芳
香族ポリエステル樹脂および4弗化エチレン樹脂の第1
表に示す割合の混合物をスプレーコーテイングし、90
〜100℃で30分間乾燥して溶剤を蒸発させた後、さ
らに280℃で30分間焼成してすべり摩擦材料とした
。実施例 3(試料/F6.7、8、9) 耐熱強化プラスチツクにコーテイングする合成樹脂混合
物の混合割合を第1表に示すようにすると共に、これに
同表に示す割合でMOS2、Pb、Grの一種または二
種を添加し、実施例1と同一の手順ですベリ摩擦材料を
作成した。
Next, polyamideimide resin (PA in Table 1) was used as an undercoat.
Spray coating a mixture of (abbreviated as I) and tetrafluoroethylene resin (abbreviated as 4F) in the proportions shown in Table 1,
Dry at 90-100°C for 30 minutes. This heat-resistant reinforced plastic, which has been undercoated, is coated with a first coat of polyamide-imide resin, aromatic polyester resin, and tetrafluoroethylene resin.
Spray coat the mixture in the proportions shown in the table and
After drying at ~100°C for 30 minutes to evaporate the solvent, it was further baked at 280°C for 30 minutes to obtain a sliding friction material. Example 3 (Sample/F6.7, 8, 9) The mixing ratio of the synthetic resin mixture to be coated on the heat-resistant reinforced plastic was as shown in Table 1, and MOS2, Pb, and Gr were added in the ratios shown in the same table. A Veri friction material was prepared in the same manner as in Example 1 by adding one or two of the following.

実施例 4(試料洗10、11、12) 第1表に示す割合の混合物により実施例2と同一の手順
で下塗を行ない、次いでMOS2、Pb、Grの一つを
同表に示す割合で添加した混合物を実施例2と同様にス
プレーコーテイングしてすべり摩擦材料を作成した。
Example 4 (Sample washing 10, 11, 12) Undercoating was performed in the same manner as in Example 2 using the mixture in the proportions shown in Table 1, and then one of MOS2, Pb, and Gr was added in the proportions shown in the table. The resulting mixture was spray coated in the same manner as in Example 2 to produce a sliding friction material.

実施例 5(試料.7V).13、14、15)実施例
1と同様の手順で作成したすベリ摩擦材料に、第1図に
模式的に示すようなオイルポケツトAを設けた。
Example 5 (Sample.7V). 13, 14, 15) An oil pocket A as schematically shown in FIG. 1 was provided in a slip friction material prepared in the same manner as in Example 1.

同図中、Bは合成樹脂のコーテイング層、Cは耐熱強化
プラスチツク、DはオイルポケツトAに保持されたグリ
スである。第1表は、上記実施例1ないし5(試料Af
)1〜※〈15)の試料にコーテイングした合成樹脂等
の組成と、比較材としての試料Al).16、17の組
成を示したものである。
In the figure, B is a synthetic resin coating layer, C is a heat-resistant reinforced plastic, and D is grease held in an oil pocket A. Table 1 shows the above Examples 1 to 5 (sample Af
) 1 to *<15) The composition of the synthetic resin coated on the samples and the sample Al) as a comparison material. The compositions of Nos. 16 and 17 are shown.

但し、試料7f6.16は4弗化エチレン樹脂の単体(
ソリツド)であり、試料廃17は裏金鋼板上に銅合金を
焼結し、その多孔質層に4弗化エチレン樹脂を含浸させ
たものである。次に、第2表は、上記各試料に対しすべ
り摩擦試験(実験1)を行なつた結果を示すもので、そ
の実験条件は次の通りである。
However, sample 7f6.16 is a simple substance of tetrafluoroethylene resin (
The sample waste 17 is made by sintering a copper alloy on a back metal plate and impregnating the porous layer with tetrafluoroethylene resin. Next, Table 2 shows the results of a sliding friction test (Experiment 1) performed on each of the above samples, and the experimental conditions are as follows.

く実験条件〉 試験機:ピン/デイスクタイプ高速すベリ摩擦試験機相
手材;MO系合金 面圧;101<9/Cd すべり速度;40m/s 給油;なし(但し、実施例5(試料.46.13、14
、15)はオイルポケツトにグリースが保持されている
Experimental conditions〉 Testing machine: Pin/disk type high-speed sliding friction tester Mating material: MO-based alloy Surface pressure: 101<9/Cd Sliding speed: 40 m/s Lubricating: None (However, Example 5 (sample. 46 .13, 14
, 15), grease is retained in the oil pocket.

)第2表に示す実験結果は、本発明に係るすべり摩擦材
料は、摩擦係数、摩耗率とも比較材のそれに比して同等
か、これより低く、良好な摩擦特性を有することを示し
ており、かつ各樹脂等の混合割合の限定理由も明らかに
している。
) The experimental results shown in Table 2 show that the sliding friction material according to the present invention has good friction properties, with both the friction coefficient and wear rate being equal to or lower than those of the comparative material. , and also clarifies the reasons for limiting the mixing ratio of each resin, etc.

すなわち、まずポリアミドイミド樹脂の混合割合が4%
である試料洗1は剥離しているが、これが10%を越え
れば使用条件にもよるが通常剥離しない。また試料./
F6.3が示すようにこの樹脂の混合割合が35%を越
えた40%となると、摩擦係数が高くなる。次に芳香族
ポリエステル樹脂は、試料應5が示すように5%を下ま
わると摩耗量の増大が見られ、また試料/16.6が示
すように35%を越えると摩擦係数が高くなる。また固
体潤滑剤については、Grを20%加えた試料滝9が剥
離しており、これを加え過ぎるとコーテイング被膜が胞
弱になることを裏付けている。なお、この実験では、剥
離の有無という点では下塗を施した実施例2および4(
試料.46.4〜6、10〜12)と下塗を施さない実
施例1および3(試料滝1〜3、7〜9)との差が認め
られなかつたが、下塗を施した方が耐熱強化プラスチツ
クとの密着強度が高くなることは明らかである。またオ
イルポケツトを設けた実施例5(試料洗13〜15)は
、摩擦係数の低いことが認められ、かつポリアミドイミ
ド樹脂が4%の試料A6.l3にも剥離が認められなか
つたので、オイルポケツトによる潤滑に効果のあること
が確認された。さらに、コスト面については、本発明に
係るすベリ摩擦材料と試料洗16のソリツド材とで同一
形状の試料を作ると、ソリツド材の方がコスト高になる
。(実験2) 試料洗2、4、9、12、17についての耐蝕試験を下
記の条件で油中に浸すことにより行なつた。
That is, first, the mixing ratio of polyamide-imide resin is 4%.
Sample wash 1, which is , peeled off, but if this exceeds 10%, it usually does not peel off, although it depends on the conditions of use. Another sample. /
As shown by F6.3, when the mixing ratio of this resin exceeds 35% to 40%, the coefficient of friction increases. Next, for aromatic polyester resins, as sample No. 5 shows, when the wear amount is less than 5%, an increase in the amount of wear is observed, and as sample /16.6 shows, when it exceeds 35%, the friction coefficient becomes high. Regarding the solid lubricant, Sample 9 with 20% Gr added peeled off, which proves that adding too much will weaken the coating. In addition, in this experiment, in terms of the presence or absence of peeling, Examples 2 and 4 (undercoated)
sample. 46.4-6, 10-12) and Examples 1 and 3 (Samples 1-3, 7-9) in which no undercoat was applied, but the heat-resistant reinforced plastic was better with the undercoat. It is clear that the adhesion strength with the material increases. In addition, Example 5 (sample washes 13 to 15), which was provided with an oil pocket, was found to have a low coefficient of friction, and sample A6. Since no peeling was observed in l3, it was confirmed that lubrication by oil pockets was effective. Furthermore, in terms of cost, if a sample of the same shape is made using the slip friction material according to the present invention and the solid material of the sample washing 16, the solid material will be more expensive. (Experiment 2) Corrosion resistance tests were conducted on samples washed 2, 4, 9, 12, and 17 by immersing them in oil under the following conditions.

第2図は、上記実験2の結果を試料重量が何即減少した
かをもつて示したものである。
FIG. 2 shows the results of Experiment 2, showing how quickly the sample weight decreased.

但し試験前の各試料の重量は、試料A6.2が7.2y
.滝4が7.17、滝9が7.27、/F6.l2が7
.07、洗17が35.47である。このグラフが示す
ように、本発明に係るすべり摩擦材料は重量減がほとん
ど認められないのに対し、比較材である試料滝17は大
幅に重量の低下しているのが認められる。
However, the weight of each sample before the test is 7.2y for sample A6.2.
.. Waterfall 4 is 7.17, Waterfall 9 is 7.27, /F6. l2 is 7
.. 07, wash 17 is 35.47. As this graph shows, the sliding friction material according to the present invention exhibits almost no weight loss, whereas the comparison material Sample Taki 17 shows a significant weight reduction.

これは試料洗17が裏金として鋼板を使用しているため
である。またこの耐蝕試験によつて試料/F6.l7の
合成樹脂皮膜層の密着強度は極めて低下し、試料の一部
に剥離する現象がみられた。このように、本発明のすべ
り摩擦材料は裏金使用の材料に比して格段耐蝕性に優れ
ており、かつ裏金を所用していないため軽量化のメリツ
トもある。(実験3) 試料A6.2、4、17について特に磁界下の摩耗特性
を調べるため下記の条件で摩擦試験を行つた。
This is because the sample washer 17 uses a steel plate as a backing metal. In addition, sample /F6. The adhesion strength of the synthetic resin film layer of No. 17 was extremely reduced, and a phenomenon of peeling was observed in some parts of the sample. As described above, the sliding friction material of the present invention has much better corrosion resistance than materials using a backing metal, and also has the advantage of being lightweight since it does not require a backing metal. (Experiment 3) A friction test was conducted on Samples A6.2, A6.2, A6.4, and A6.17 under the following conditions in order to particularly investigate the wear characteristics under a magnetic field.

(実験条件)試験機;機械試験場型摩擦摩耗試験機 相手材,永久磁石(MCAl5O) 面圧;10k9/Cd すベリ速度;1,5m/Sec 給油;オイルバス中(但しFe2O3の200メツシユ
以下を0.5y/l混入)時間,5分間 第3図は、上記実験3の結果を試料重量が何ワ減少した
かをもつて示したものであつて、試験前の各試料の重量
は、試料,46.2が7.37、洗4が7.2y,..
/F6.l7が35.27であつた。
(Experiment conditions) Testing machine: Mechanical testing site type friction and wear tester Mating material: permanent magnet (MCAl5O) Surface pressure: 10k9/Cd Slip speed: 1.5m/Sec Lubricating: In oil bath (however, less than 200 meshes of Fe2O3 Figure 3 shows the results of Experiment 3 above, showing how much the sample weight decreased.The weight of each sample before the test was , 46.2 is 7.37, wash 4 is 7.2y, . ..
/F6. l7 was 35.27.

このグラフから明らかなように、裏金鋼板を使用した試
料滝17は試験時間の経過と共に急カーブで重量が減少
しているのに対し、本発明に係る摩擦材料(試料716
2、4)は重量減が少なく、両者の重量減の差は時間が
経つ程大となつている。これは摩擦試験の相手材である
永久磁石(MCAl5O)がオイルバス中のFe2O3
粉を巻き込むため、裏金鋼板を有する試料A6.l7で
はこのFe2O3粉によりアブレシブ摩耗を起こしてい
るのに対し、本発明の摩擦材料は耐熱強化プラスチツク
を使用しているのでFe2O3粉の巻き込みによるアブ
レシブ摩耗が少ないことを示しているものと解される。
以上説明した通り、本発明に係るすベリ摩擦材料は、従
来の裏金鋼板使用の摩擦材料や合成樹脂単体よりなる摩
擦材料に比して摩耗率、摩擦係数が低いと共にコスト的
にも安く、また基板が耐熱強化プラスチツクよりなるの
で、耐蝕性に優れ、かつ軽量である。
As is clear from this graph, the weight of sample Taki 17 using a backing steel plate decreases due to sharp curves as the test time passes, whereas the friction material according to the present invention (sample 716
2 and 4) have less weight loss, and the difference in weight loss between the two becomes larger as time passes. This is because the permanent magnet (MCAl5O), which is the material to be tested in the friction test, is Fe2O3 in an oil bath.
Sample A6. has a steel backing plate to trap powder. This can be interpreted as indicating that abrasive wear caused by this Fe2O3 powder is caused in 17, whereas the friction material of the present invention uses heat-resistant reinforced plastic, so there is less abrasive wear due to the entrainment of Fe2O3 powder. .
As explained above, the sliding friction material according to the present invention has a lower wear rate and coefficient of friction than conventional friction materials using a backing steel plate or friction materials made of a single synthetic resin, and is also cheaper in cost. Since the substrate is made of heat-resistant reinforced plastic, it has excellent corrosion resistance and is lightweight.

さらに磁界下での鉄粉の巻き込みによるアブレシブ摩耗
が少ないので、磁界下で使用するすべり摩擦材料として
有利であつて、また摺動部材間の絶縁が容易に得られる
ので、絶縁を必要とする軸と軸受、軸とハウジング等に
使用できる等、極めて広範な用途に使用できるものであ
る。
Furthermore, since there is little abrasive wear due to entrainment of iron powder under a magnetic field, it is advantageous as a sliding friction material used under a magnetic field, and insulation between sliding members can be easily obtained, so it can be used for shafts that require insulation. It can be used for an extremely wide range of applications, including bearings, shafts, and housings.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は、本発明に係るすべり摩擦材料にオイルポケツ
トを形成した状態を示す模式的断面図、第2図、第3図
は、それぞれ耐蝕試験、摩擦試験の結果を示すグラフで
ある。
FIG. 1 is a schematic sectional view showing a state in which oil pockets are formed in the sliding friction material according to the present invention, and FIGS. 2 and 3 are graphs showing the results of a corrosion resistance test and a friction test, respectively.

Claims (1)

【特許請求の範囲】 1 耐熱強化プラスチック上に、重量%で10〜35%
の接着性樹脂と5〜35%の芳香族ポリエステル樹脂お
よび残部が4弗化エチレン樹脂からなる混合物をコーテ
ィングし、これを乾燥、焼成してなるすべり摩擦材料。 2 耐熱強化プラスチックに、接着性樹脂と4弗化エチ
レン樹脂との混合物による下塗が施されている特許請求
の範囲第1項に記載のすべり摩擦材料。 3 耐熱強化プラスチック上に、重量%で10〜35%
の接着性樹脂、5〜35%の芳香族ポリエステル樹脂、
1〜15%の一種または二種以上の固体潤滑剤、および
残部が4弗化エチレン樹脂からなる混合物をコーティン
グし、これを乾燥、焼成してなるすべり摩擦材料。 4 耐熱強化プラスチックに、接着性樹脂と4弗化エチ
レン樹脂との混合物による下塗が施されている特許請求
の範囲第3項に記載のすべり摩擦材料。
[Claims] 1. 10 to 35% by weight on heat-resistant reinforced plastic
A sliding friction material obtained by coating a mixture of an adhesive resin, 5 to 35% aromatic polyester resin, and the balance consisting of tetrafluoroethylene resin, drying and baking the mixture. 2. The sliding friction material according to claim 1, wherein the heat-resistant reinforced plastic is undercoated with a mixture of adhesive resin and tetrafluoroethylene resin. 3 10-35% by weight on heat-resistant reinforced plastic
adhesive resin, 5-35% aromatic polyester resin,
A sliding friction material coated with a mixture consisting of 1 to 15% of one or more solid lubricants and the balance consisting of a tetrafluoroethylene resin, dried and fired. 4. The sliding friction material according to claim 3, wherein the heat-resistant reinforced plastic is undercoated with a mixture of adhesive resin and tetrafluoroethylene resin.
JP1224777A 1977-02-07 1977-02-07 sliding friction material Expired JPS5945006B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1224777A JPS5945006B2 (en) 1977-02-07 1977-02-07 sliding friction material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1224777A JPS5945006B2 (en) 1977-02-07 1977-02-07 sliding friction material

Publications (2)

Publication Number Publication Date
JPS5397075A JPS5397075A (en) 1978-08-24
JPS5945006B2 true JPS5945006B2 (en) 1984-11-02

Family

ID=11800027

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1224777A Expired JPS5945006B2 (en) 1977-02-07 1977-02-07 sliding friction material

Country Status (1)

Country Link
JP (1) JPS5945006B2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62130505U (en) * 1986-02-12 1987-08-18
JPS63107605U (en) * 1986-12-29 1988-07-11
JPH0314085Y2 (en) * 1984-12-10 1991-03-29

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62201996A (en) * 1986-02-28 1987-09-05 Nok Corp Member for sliding portion
JPH0324196A (en) * 1989-06-20 1991-02-01 Daido Metal Co Ltd Composite resin sliding member
DE102011109362A1 (en) * 2011-08-04 2013-02-07 Thyssen Krupp Bilstein Suspension GmbH Shock absorber for a vehicle in lightweight construction
FR2999670B1 (en) * 2012-12-13 2014-11-28 Hydromecanique & Frottement GUIDE ARRANGEMENT IN THE FORM OF A METAL RING FOR FITTING WITH FRICTION AND WITH ARTICULATING AND / OR SLIDING CAPACITY OF AXIS.

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0314085Y2 (en) * 1984-12-10 1991-03-29
JPS62130505U (en) * 1986-02-12 1987-08-18
JPS63107605U (en) * 1986-12-29 1988-07-11

Also Published As

Publication number Publication date
JPS5397075A (en) 1978-08-24

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