JPS58109542A - Slide surface forming material - Google Patents

Slide surface forming material

Info

Publication number
JPS58109542A
JPS58109542A JP21028881A JP21028881A JPS58109542A JP S58109542 A JPS58109542 A JP S58109542A JP 21028881 A JP21028881 A JP 21028881A JP 21028881 A JP21028881 A JP 21028881A JP S58109542 A JPS58109542 A JP S58109542A
Authority
JP
Japan
Prior art keywords
fine powder
friction
coated
binder resin
mixed
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.)
Granted
Application number
JP21028881A
Other languages
Japanese (ja)
Other versions
JPS5844696B2 (en
Inventor
Yoshiaki Terauchi
寺内淑晃
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.)
MIKASA PAINT KK
Original Assignee
MIKASA PAINT KK
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 MIKASA PAINT KK filed Critical MIKASA PAINT KK
Priority to JP21028881A priority Critical patent/JPS5844696B2/en
Publication of JPS58109542A publication Critical patent/JPS58109542A/en
Publication of JPS5844696B2 publication Critical patent/JPS5844696B2/en
Expired legal-status Critical Current

Links

Abstract

PURPOSE:To provide the titled material showing an excellent effect of reducing the coefficient of friction for a long period of time, obtained by a method wherein a fine powder of a substance having a low slide friction resistance and a high wear resistance is coated with a silicon oil and the coated powder is mixed with a binder resin containing a silicon coupling agent. CONSTITUTION:A fine powder of a substance having a low slide friction resistance and a high wear resistance, such as Teflon, polyethylene, polypropylene, boron nitride or graphite, is prepared and the surface thereof is coated with a thin silicone oil film with a thickness of several molecules or less to increase the contact angle of the surface of the fine powder. In the next step, about 50-150pts.wt. treated fine powder is mixed with 100pts.wt. binder resin and a silicone coupling agent is compounded therein in order to enhance the bonding force of the fine powder and the binder resin to obtain an objective slide surface forming material. The obtained material is applied on the surface of a weather strip rubber to be suitably used in lowering the coefficient of friction.

Description

【発明の詳細な説明】 本発明は摺動面形成材料に係るもσ)で、自動車の左右
窓カラスと雨水浸入防止用のゴム片−建築用サツシのガ
ラス面と気密保持用のコム片の如く、ゴム又はプラスチ
ック成形品の表面とガラス面又は金属面と接触して摺動
する部材に付寿し、すべり摩擦係数を低下させ摺動を容
易にしようとするものである。この種の目的を達成する
ためコ゛ム又はプラスチックの表面に摩擦係数が小さな
物質を付着し摺動な容易とする方法は従来押り試みられ
ているがいずれも好ましいものではなかった。その中で
も広く用いられてきたのは摩擦係数の小さな物質で形成
した微粉末を合成樹脂等適当な結合材料に混入混合し、
この混合物を目的部に塗布して摺動面を形成する方法で
ある。この方法は摺動面を形成するための作業性が良い
利点を有するが、従来品は耐摩耗性が悪く慴動摩擦に耐
えられない欠点を有し、摩擦係数減少効果の持続性がな
い欠点を有していた。その原因の第1は摩擦係数の小さ
な物質で形成した微粉末と結合材料との付着性が悪く摺
動の繰返しによって微粉末の脱落が生じることにある。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a sliding surface forming material. This is attached to a member that slides in contact with the surface of a rubber or plastic molded product and a glass surface or a metal surface in order to reduce the coefficient of sliding friction and facilitate sliding. In order to achieve this kind of objective, attempts have been made to attach a substance with a small coefficient of friction to the surface of a comb or plastic to make it easier to slide, but none of these methods were desirable. Among these, the most widely used method is to mix fine powder made of a substance with a small coefficient of friction with a suitable binding material such as synthetic resin.
This is a method in which this mixture is applied to a target part to form a sliding surface. This method has the advantage of good workability for forming sliding surfaces, but conventional products have the disadvantage of poor wear resistance and cannot withstand sliding friction, and the disadvantage that the effect of reducing the coefficient of friction is not sustainable. had. The first reason for this is that the adhesion between the fine powder made of a substance with a small coefficient of friction and the bonding material is poor, and repeated sliding causes the fine powder to fall off.

第2に微粉末の外周を結合材料が被覆してしまい摺動の
初期には摩擦抵抗の大きな結合材料とガラス、金属等の
摺動面とが接触し相当程度摺動が繰返されて結合材料の
表面が発熱摩耗脱落した後に微粉末が露頭して初めて摩
擦抵抗を低下させることが可能となる点にある。第3に
微粉末の粒度が小さすぎると、塗布部表面の平滑度が増
大し摺動面の接触面積が増大し摩擦による発熱摩耗等を
受けやすくなることにある。
Second, the outer periphery of the fine powder is covered with the bonding material, and at the beginning of sliding, the bonding material with high frictional resistance comes into contact with the sliding surface of glass, metal, etc., and the sliding is repeated to a considerable extent. The point is that it becomes possible to reduce the frictional resistance only when the fine powder is exposed after the surface of the friction layer has been worn off due to heat generation. Thirdly, if the particle size of the fine powder is too small, the smoothness of the surface of the applied part increases, the contact area of the sliding surface increases, and it becomes susceptible to heat-generating wear due to friction.

本発明は上述の如き欠点を除去し摩擦抵抗の小ざな摺動
面を強固に形成し長期間の使用に元号耐えることができ
る摺動面形成材料に係るものである。本発明に於ても摩
擦抵抗の小さな物質で形成した微粉末を結合材料に混入
混合するものであるが、微粉末と結合材料との付層性を
向上させ微粉リング剤を使用することを特徴としている
The present invention relates to a material for forming a sliding surface that eliminates the above-mentioned drawbacks, forms a strong sliding surface with low frictional resistance, and can withstand long-term use. In the present invention, fine powder made of a substance with low frictional resistance is mixed into the binding material, but the feature is that a fine powder ring agent is used to improve the layering properties between the fine powder and the binding material. It is said that

滑り摩擦抵抗の小さく且耐摩耗性の大きな物質、例えば
カラスに対する静摩擦係数が0.5以下のテフロン、ポ
リエチレン、ポリプロピレン、窒化ホウ素、グラフ了イ
ト等の微粉末の表面を、シリコーン油の数分子以下の薄
膜で被覆し、微粉末表面の接触角を増大させる。“この
微粉末をポリイソシアネート樹脂、アクリル樹脂、エポ
キシ樹脂等の結合材料中に混入混合する。この結合材料
と微粉末とは、結合材料中で微粉末が上層から下層まで
光分位置し得るようその混合比率を定めなければならな
い。−例としては結合材料100重量部に対し50〜1
50重鰍部の範囲で微粉末を混合する。この微粉末はシ
リコーン油の薄膜で被儂されているから表面の接触角を
増大させ結合材料樹脂による儒れが最小となり上層に位
置する微粉末は結合材料樹脂表面への露頭を可能とする
。又シリコーン油はそれ自体が潤滑性を有するので摺動
の初期から摩擦抵抗の低下を期待し得るものとなる。
The surface of a fine powder such as a substance with low sliding friction resistance and high wear resistance, such as Teflon, polyethylene, polypropylene, boron nitride, graphite, etc., whose coefficient of static friction against glass is 0.5 or less, is coated with a few molecules or less of silicone oil. coated with a thin film of powder to increase the contact angle on the surface of the fine powder. “This fine powder is mixed into a binding material such as polyisocyanate resin, acrylic resin, or epoxy resin. The mixing ratio must be determined - for example, 50 to 1
Mix fine powder within the range of 50 gills. Since the fine powder is coated with a thin film of silicone oil, it increases the contact angle on the surface, minimizes flaking by the binder resin, and allows the fine powder located in the upper layer to outcrop onto the binder resin surface. Furthermore, since silicone oil itself has lubricating properties, it can be expected to reduce frictional resistance from the initial stage of sliding.

しかしながら微粉末と結合材料の藺れを最小とすること
は反面微粉末と結合材料の結合性をも低下させ、微粉末
の脱落を生じるものとなる。
However, minimizing the smearing between the fine powder and the binding material also reduces the bonding properties between the fine powder and the binding material, causing the fine powder to fall off.

そこで結合材料樹脂中にシリコーンカップリンク剤を共
存させる。このシリコーンカップリンク剤は微粉末會被
僚したシリコーン油の無機部分と結合するとともに結合
材料樹脂の有機分と結合する。微粉末表面を被覆するシ
リコーン油膜の厚さが数分子以下であればファンデルワ
ールス力とカップリング剤の結合力により微粉末と結合
材料樹脂との強固な付着性を得ることができる。
Therefore, a silicone coupling agent is made to coexist in the binding material resin. The silicone coupling agent combines with the inorganic portion of the finely powdered silicone oil and the organic portion of the binder resin. If the thickness of the silicone oil film covering the surface of the fine powder is several molecules or less, strong adhesion between the fine powder and the binding material resin can be obtained due to the van der Waals force and the binding force of the coupling agent.

実施例 ナイロンパラター (平均粒径5〜20μ]    225重量部ジメチル
ポリシロキサン      24重敞部ポリイソシアネ
ート樹脂     4.00”ポリエーテルポリオール
      B□  //シリコーンカツフ゛リング剤
     30//酢酸エチレングリコールモノ   
 41//エチルエーテル トリオール              200 〃製
造方法 ジメチルポリシロキサン(シリコーン油) t−)リオ
ールに溶解し、ジメチルポリシロキサン(シリコーン油
)のドルオール溶解液を形成し、この溶解Rkナイロン
バウターと混合した後、1時間以上静置してジメチルポ
リシロキサン(シリコーン油)をナイロンバラタ−の表
面に薄く被覆する。
Examples Nylon paratar (average particle size 5 to 20μ) 225 parts by weight dimethylpolysiloxane 24 parts by weight Polyisocyanate resin 4.00” polyether polyol B□ //Silicone cutting agent 30//Ethylene glycol monoacetate
41//Ethyl ether triol 200 〃Manufacturing method Dimethylpolysiloxane (silicone oil) t-) Dissolved in liol to form a doluol solution of dimethylpolysiloxane (silicone oil), and mixed with this dissolved Rk nylon batter. Thereafter, the surface of the nylon balater is thinly coated with dimethylpolysiloxane (silicone oil) by allowing it to stand for at least 1 hour.

このシリコーン油で被!シたす1〒ンパウダーを風乾す
る。別個にポリエーテルポリオール、シリコーンカップ
リング剤、酢酸エチレングIJコールモノエチルエーテ
ルを良く混合し混合液を形成する。この混合液にシリコ
ーン前にて被徨済のナイロンパウダーを混入混合し良く
攪拌する。使用にあたってはこれにイソシアネートを加
えて攪拌し、エアスプレー塗装機等を使用してウエサー
ストリツフゴム基材の表面に塗布した後、120℃で3
0分間乾燥を打なう。このウェザ−ストリップゴム基材
を、学術振興型耐摩耗性試験機によって試験を行なった
ところ、乾式試験および湿式試験で10,000回(荷
重IKjE、7ii’温ン以上の性能を示した。また上
記ウェザ−ストリッツゴム基材を用いて自動車の窓枠を
組立て窓カラスの昇降機構の上向および下向のトルクラ
測定した。その結果上向2.2 K P −cm/se
c 、下向1.6Ky−cm/secの値が得られ、植
毛を施した従来品の上向3.2 KP−cm/sθC1
下向2.4. KP−cm/secと比較し摺動抵抗の
低下が顯著に認められた。
Cover with this silicone oil! Air dry the powder. Separately, polyether polyol, silicone coupling agent, and acetic acid ethylene glycol monoethyl ether are thoroughly mixed to form a mixed solution. The mixed nylon powder is mixed into this mixed solution before the silicone, and the mixture is thoroughly stirred. To use, add isocyanate to it, stir it, apply it to the surface of the watherstriff rubber base material using an air spray coating machine, etc.
Let dry for 0 minutes. When this weatherstrip rubber base material was tested using an abrasion resistance testing machine for the promotion of science, it showed performance of 10,000 times (load IKjE, 7ii' warm) or more in dry and wet tests. An automobile window frame was assembled using the above Weatherstritz rubber base material, and the upward and downward torque vibrations of the window glass elevating mechanism were measured.The upward torque was 2.2 K P -cm/se.
c, a value of 1.6 Ky-cm/sec in the downward direction was obtained, and a value of 3.2 KP-cm/sθC1 in the upward direction of the conventional product with flocking
Downward 2.4. A marked decrease in sliding resistance was observed compared to KP-cm/sec.

Claims (1)

【特許請求の範囲】[Claims] 滑り摩擦抵抗が小さく且耐摩耗性の大きな物質で形成し
た微粉末をシリコーン油の数分子以下の簿膜で被覆しこ
の微粉末をシリコーンカンフ11ング剤を共存させた結
合材料樹脂中に混入混合して形成することを特徴とする
摺動面形成材料。
A fine powder made of a material with low sliding friction resistance and high wear resistance is coated with a film of silicone oil of several molecules or less, and this fine powder is mixed into a binding material resin in which a silicone cuffing agent is coexisting. A sliding surface forming material characterized by being formed by.
JP21028881A 1981-12-24 1981-12-24 Sliding surface forming material Expired JPS5844696B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21028881A JPS5844696B2 (en) 1981-12-24 1981-12-24 Sliding surface forming material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP21028881A JPS5844696B2 (en) 1981-12-24 1981-12-24 Sliding surface forming material

Publications (2)

Publication Number Publication Date
JPS58109542A true JPS58109542A (en) 1983-06-29
JPS5844696B2 JPS5844696B2 (en) 1983-10-05

Family

ID=16586911

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21028881A Expired JPS5844696B2 (en) 1981-12-24 1981-12-24 Sliding surface forming material

Country Status (1)

Country Link
JP (1) JPS5844696B2 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61157727A (en) * 1984-12-28 1986-07-17 Honda Motor Co Ltd Throttle body for internal-combustion engine
EP0812875A1 (en) * 1996-06-13 1997-12-17 Valeo Systemes D'essuyage Coating solution and wiper blade coated with such a solution
US6175986B1 (en) 1996-06-13 2001-01-23 Valeo Systemes D'essuyage Wiping strip for a motor vehicle screen wiper
US7247673B2 (en) 2003-04-30 2007-07-24 National Starch And Chemical Investment Holding Corporation Waterbased high abrasion resistant coating
CN106752117A (en) * 2016-12-12 2017-05-31 深圳德邦界面材料有限公司 Modified graphite and preparation method thereof, organic siliconresin

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61157727A (en) * 1984-12-28 1986-07-17 Honda Motor Co Ltd Throttle body for internal-combustion engine
EP0812875A1 (en) * 1996-06-13 1997-12-17 Valeo Systemes D'essuyage Coating solution and wiper blade coated with such a solution
FR2749852A1 (en) * 1996-06-13 1997-12-19 Valeo Systemes Dessuyage SOLUTION FOR REALIZING A COATING ON A PROFILE, WIPING BLADE COATED WITH SUCH A SOLUTION, METHOD FOR COATING A PROFILE WITH SUCH A COATING AND WIPING BLADE COATED WITH A COATING, OBTAINED BY SUCH A PROCESS
US5883168A (en) * 1996-06-13 1999-03-16 Valeo Systemes D'essuyage Aqueous emulsion or dispersion for forming a coating on a profiled element
US5989641A (en) * 1996-06-13 1999-11-23 Valeo Systemes D'essuyage Profiled element coated with an aqueous emulsion or dispersion
US6010752A (en) * 1996-06-13 2000-01-04 Valeo Systemes D'essuyage Method for coating a profiled element with an aqueous emulsion or dispersion
US6175986B1 (en) 1996-06-13 2001-01-23 Valeo Systemes D'essuyage Wiping strip for a motor vehicle screen wiper
US7247673B2 (en) 2003-04-30 2007-07-24 National Starch And Chemical Investment Holding Corporation Waterbased high abrasion resistant coating
CN106752117A (en) * 2016-12-12 2017-05-31 深圳德邦界面材料有限公司 Modified graphite and preparation method thereof, organic siliconresin

Also Published As

Publication number Publication date
JPS5844696B2 (en) 1983-10-05

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