JP2903709B2 - Surface coating member - Google Patents
Surface coating memberInfo
- Publication number
- JP2903709B2 JP2903709B2 JP3507549A JP50754991A JP2903709B2 JP 2903709 B2 JP2903709 B2 JP 2903709B2 JP 3507549 A JP3507549 A JP 3507549A JP 50754991 A JP50754991 A JP 50754991A JP 2903709 B2 JP2903709 B2 JP 2903709B2
- Authority
- JP
- Japan
- Prior art keywords
- parts
- member according
- weight
- coated
- resin
- 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 - Fee Related
Links
- 239000011248 coating agent Substances 0.000 title description 4
- 238000000576 coating method Methods 0.000 title description 4
- 229920001971 elastomer Polymers 0.000 claims description 28
- 229920005989 resin Polymers 0.000 claims description 28
- 239000011347 resin Substances 0.000 claims description 28
- 239000005060 rubber Substances 0.000 claims description 28
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 22
- 229910002804 graphite Inorganic materials 0.000 claims description 21
- 239000010439 graphite Substances 0.000 claims description 21
- 239000000314 lubricant Substances 0.000 claims description 20
- 239000007787 solid Substances 0.000 claims description 17
- 239000003795 chemical substances by application Substances 0.000 claims description 15
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical group S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 claims description 14
- 229910052982 molybdenum disulfide Inorganic materials 0.000 claims description 14
- 239000011159 matrix material Substances 0.000 claims description 13
- -1 polytetrafluoroethylene Polymers 0.000 claims description 13
- 229920001567 vinyl ester resin Polymers 0.000 claims description 13
- 239000011247 coating layer Substances 0.000 claims description 11
- 150000002222 fluorine compounds Chemical class 0.000 claims description 8
- 229920001343 polytetrafluoroethylene Polymers 0.000 claims description 8
- 239000004810 polytetrafluoroethylene Substances 0.000 claims description 8
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims description 7
- 239000002245 particle Substances 0.000 claims description 6
- 229920001187 thermosetting polymer Polymers 0.000 claims description 6
- 229920001296 polysiloxane Polymers 0.000 claims description 4
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims description 3
- 229920006026 co-polymeric resin Polymers 0.000 claims description 3
- 238000012856 packing Methods 0.000 claims description 3
- 238000013329 compounding Methods 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- ITRNXVSDJBHYNJ-UHFFFAOYSA-N tungsten disulfide Chemical compound S=[W]=S ITRNXVSDJBHYNJ-UHFFFAOYSA-N 0.000 claims description 2
- QLOAVXSYZAJECW-UHFFFAOYSA-N methane;molecular fluorine Chemical compound C.FF QLOAVXSYZAJECW-UHFFFAOYSA-N 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 20
- 239000012948 isocyanate Substances 0.000 description 11
- 150000002513 isocyanates Chemical class 0.000 description 11
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 10
- 229920002554 vinyl polymer Polymers 0.000 description 10
- 239000000126 substance Substances 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 8
- 229920003023 plastic Polymers 0.000 description 8
- 239000004033 plastic Substances 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 4
- 230000002159 abnormal effect Effects 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229910052750 molybdenum Inorganic materials 0.000 description 4
- 239000011733 molybdenum Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 239000004721 Polyphenylene oxide Substances 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229920002635 polyurethane Polymers 0.000 description 3
- 239000004814 polyurethane Substances 0.000 description 3
- 229920003051 synthetic elastomer Polymers 0.000 description 3
- 239000005061 synthetic rubber Substances 0.000 description 3
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 2
- 244000043261 Hevea brasiliensis Species 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 229920003049 isoprene rubber Polymers 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229920003052 natural elastomer Polymers 0.000 description 2
- 229920001194 natural rubber Polymers 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 230000002093 peripheral effect Effects 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920006324 polyoxymethylene Polymers 0.000 description 2
- 229920005749 polyurethane resin Polymers 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 238000004381 surface treatment Methods 0.000 description 2
- DHKHKXVYLBGOIT-UHFFFAOYSA-N 1,1-Diethoxyethane Chemical compound CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- CFEMBVVZPUEPPP-UHFFFAOYSA-N 2-methylbuta-1,3-diene;prop-2-enenitrile Chemical compound C=CC#N.CC(=C)C=C CFEMBVVZPUEPPP-UHFFFAOYSA-N 0.000 description 1
- JMMZCWZIJXAGKW-UHFFFAOYSA-N 2-methylpent-2-ene Chemical compound CCC=C(C)C JMMZCWZIJXAGKW-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- 229920002943 EPDM rubber Polymers 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229930182556 Polyacetal Natural products 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004962 Polyamide-imide Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004695 Polyether sulfone Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004734 Polyphenylene sulfide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- IDCBOTIENDVCBQ-UHFFFAOYSA-N TEPP Chemical compound CCOP(=O)(OCC)OP(=O)(OCC)OCC IDCBOTIENDVCBQ-UHFFFAOYSA-N 0.000 description 1
- 229920006311 Urethane elastomer Polymers 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000011354 acetal resin Substances 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- 229920002877 acrylic styrene acrylonitrile Polymers 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 229920003180 amino resin Polymers 0.000 description 1
- 208000003464 asthenopia Diseases 0.000 description 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229920000554 ionomer Polymers 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920002312 polyamide-imide Polymers 0.000 description 1
- 229920001230 polyarylate Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920006380 polyphenylene oxide Polymers 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 150000004763 sulfides Chemical class 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Lubricants (AREA)
Description
【発明の詳細な説明】 技術分野 本発明は表面被覆部材に係り、特にワイパーブレー
ド、シールパッキン、Oリング、ウェザーストリップ、
グラスラン、タイミングベルト、ゴム蛇腹、ギヤ、ドア
キャッチなどのゴムやプラスチックの表面に潤滑被覆を
施した表面被覆部材に関する。本発明は、特にワイパー
ブレード、グラスラン、ウェザーストリップ、Oリング
など、表面が他の部材と摺動する表面被覆摺動部材に好
適な表面被覆部材に関する。Description: TECHNICAL FIELD The present invention relates to a surface covering member, and particularly to a wiper blade, a seal packing, an O-ring, a weather strip,
The present invention relates to a surface covering member in which a surface of rubber or plastic such as a glass run, a timing belt, a rubber bellows, a gear, and a door catch is lubricated. The present invention relates to a surface covering member suitable for a surface covering sliding member whose surface slides with another member, such as a wiper blade, a glass run, a weather strip, and an O-ring.
背景技術 従来、ワイパーブレードゴムには天然ゴム、合成ゴム
などの成形品が用いられてきた。しかしながらこの種の
ワイパーゴムには次のような欠点があり、必ずしも,満
足されるものではなかった。BACKGROUND ART Conventionally, molded products such as natural rubber and synthetic rubber have been used as wiper blade rubber. However, this type of wiper rubber has the following drawbacks, and is not always satisfactory.
即ち、半乾燥時あるいは冷寒時ワイパーブレードゴム
とガラス面との間に付着現象が起こり、ワイパーの作動
が停止するいわゆる“ロック現象”や摩擦係数の速度依
存性が負特性を示すことによる自励振動、いわゆる“び
びり現象”が発生し、払拭不良、ブレードゴム表面
の異常摩耗、ワイパーシステムの接続各部の寿命短
縮、作動モータの消費電力の増大、“びびり現象”
による目障りおよび耳障り、などの問題点があった。That is, during semi-dry or cold weather, an adhesion phenomenon occurs between the wiper blade rubber and the glass surface, and the so-called “lock phenomenon” in which the operation of the wiper is stopped, and the speed dependence of the friction coefficient shows a negative characteristic, which is a self-locking phenomenon. Excitation vibration, so-called "chatter phenomenon" occurs, poor wiping, abnormal wear of the blade rubber surface, shortened life of each part of the wiper system connection, increased power consumption of the operating motor, "chatter phenomenon"
There are problems such as discomfort and eyestrain.
これらの問題点を解決するために、特開昭55−15873
号にて、二硫化モリブデンを含有するシリコーン組成物
をワイパーブレードゴム表面に被覆することが提案され
た。To solve these problems, Japanese Patent Application Laid-Open No. 55-15873
It has been proposed to cover a wiper blade rubber surface with a silicone composition containing molybdenum disulfide.
ところが、この被覆を有する特開昭55−15873号のワ
イパーブレードゴムにあっては、被覆層の耐久性が不足
することが見出された。これはウェザーストリップ、グ
ラスランについても同様の問題である。However, it has been found that the durability of the coating layer is insufficient in the wiper blade rubber of JP-A-55-15873 having this coating. This is the same problem for weather strips and glass runs.
また、金属面とゴム材との間についても次のような欠
点があり、必ずしも満足される特性を有していない。In addition, there is the following defect between the metal surface and the rubber material, and it does not always have satisfactory characteristics.
即ち、オイルシールやガソリンキャップシールは、ゴ
ムと金属面との間に固着現象が起こり、開閉時に高トル
クになる。Oリング、パッキン、タイミングベルト等に
ついてはゴムと金属面との摺動抵抗が高いことにより異
常摩耗、ステックスリップ、音鳴きの発生がある。ゴム
蛇腹についても異常摩耗より穴あきが発生する。また、
ポリアセタール、ナイロン樹脂等のギヤ、ドアキャッチ
などは、異常摩耗、音鳴き、きしみ音等が発生する。That is, the oil seal and the gasoline cap seal stick to each other between the rubber and the metal surface, resulting in a high torque at the time of opening and closing. O-rings, packings, timing belts and the like may cause abnormal wear, stick slip, and squeal due to high sliding resistance between the rubber and the metal surface. Holes also occur in rubber bellows due to abnormal wear. Also,
Gears such as polyacetal and nylon resin, door catches, and the like generate abnormal wear, squeal, and squeak.
これらも問題点を解決するためにグリース等を塗布す
る処置が施されているが耐久性が不足することが見出さ
れている。These are also treated by applying grease or the like to solve the problem, but it has been found that durability is insufficient.
発明の開示 本発明の目的は、上記の問題点を解決し、摺動性がき
わめて良好であると共に、被覆層の耐久性も高い表面被
覆部材を提供することにある。DISCLOSURE OF THE INVENTION An object of the present invention is to solve the above problems and to provide a surface covering member having extremely good slidability and high durability of a covering layer.
本発明の表面被覆部材は、固体潤滑剤及び樹脂マトリ
ックスを含んでなる被覆層が表面に形成されている表面
被覆部材であって、該硬化剤によって硬化された熱硬化
樹脂であり、該熱硬化樹脂がフルオロオレフィンビニー
ルエーテルビニールエステル共重合体樹脂であることを
特徴とするものである。The surface-coated member of the present invention is a surface-coated member having a coating layer containing a solid lubricant and a resin matrix formed on a surface thereof, and is a thermosetting resin cured by the curing agent; The resin is a fluoroolefin vinyl ether vinyl ester copolymer resin.
本発明の表面被覆部材の本体部分を構成するゴム又は
プラスチックは、特に制限されるものではなく、各種の
ゴム、プラスチックを採用できる。ゴムは天然ゴム、合
成ゴムのいずれでも良い。合成ゴムの一例をあげるなら
ば、スチレンブタジエンゴム、ブタジエンゴム、イソプ
レンゴム、エチレンプロピレンゴム(EPM、EPDM)、ア
クリロニトリルブタジエンゴム、クロロプレンゴム、イ
ソブチレンイソプレンゴム、アルフィンゴム、ポリエー
テルゴム、多硫化ゴム、シリコンゴム、アクリルゴム、
フッ素ゴム、ハロゲン化ポリエチレンゴム、ウレタンゴ
ム、エチレン酢酸ビニルゴム、ハイスチレンゴム、アク
リロニトリルイソプレンゴムなどである。このうち、EP
DMが好ましい。The rubber or plastic constituting the main body of the surface covering member of the present invention is not particularly limited, and various rubbers and plastics can be employed. The rubber may be either natural rubber or synthetic rubber. Examples of synthetic rubber include styrene butadiene rubber, butadiene rubber, isoprene rubber, ethylene propylene rubber (EPM, EPDM), acrylonitrile butadiene rubber, chloroprene rubber, isobutylene isoprene rubber, alphin rubber, polyether rubber, polysulfide rubber, Silicone rubber, acrylic rubber,
Examples include fluorine rubber, halogenated polyethylene rubber, urethane rubber, ethylene vinyl acetate rubber, high styrene rubber, acrylonitrile isoprene rubber, and the like. Of these, EP
DM is preferred.
プラスチックとしては、熱硬化性樹脂、熱可塑性樹脂
のいずれでも良い。As the plastic, either a thermosetting resin or a thermoplastic resin may be used.
プラスチックの一例をあげるならば、ABS樹脂、ABSブ
レンド、アセタール樹脂(ホモポリマー)、アクリル樹
脂、ACS樹脂、アルキド樹脂、アミノ樹脂、ASA樹脂、セ
ルロース系樹脂、塩素化ポリエーテル、ジアリルフタレ
ート樹脂、エポキシ樹脂、エチレン酢酸ビニル共重合
体、ふっ素樹脂、アイオノマー、メチルペンテンポリマ
ー、フェノール樹脂、ポリアミド(ナイロン)、ポリア
リルエーテル、ポリアリルスルホン、ポリプテン−1、
ポリカーボネート、不飽和ポリエステル樹脂、ポリエチ
レン、ポリエチレンテレフタレート(テトロン)、ポリ
イミド、ポリアミドイミド、ポリフェニレンオキサイ
ド、ポリフェニレンスルフィド、ポリプロピレン、ポリ
スチレン、ポリスルホン、ポリエーテルスルホン、ポリ
ウレタン、塩化ビニル樹脂、ポリアリレートである。Examples of plastics include ABS resin, ABS blend, acetal resin (homopolymer), acrylic resin, ACS resin, alkyd resin, amino resin, ASA resin, cellulosic resin, chlorinated polyether, diallyl phthalate resin, and epoxy. Resin, ethylene vinyl acetate copolymer, fluororesin, ionomer, methylpentene polymer, phenolic resin, polyamide (nylon), polyallyl ether, polyallyl sulfone, polybutene-1,
Polycarbonate, unsaturated polyester resin, polyethylene, polyethylene terephthalate (tetron), polyimide, polyamide imide, polyphenylene oxide, polyphenylene sulfide, polypropylene, polystyrene, polysulfone, polyether sulfone, polyurethane, vinyl chloride resin, and polyarylate.
このゴム又はプラスチックを被覆する被覆層は、固体
潤滑剤と樹脂マトリックスとを含んでなる。The coating layer covering the rubber or plastic comprises a solid lubricant and a resin matrix.
樹脂マトリックスは硬化剤により硬化された熱硬化樹
脂であり、該熱硬化樹脂としてはフルオロオレフィンビ
ニールエーテルビニールエステル共重合体樹脂が用いら
れる。The resin matrix is a thermosetting resin cured by a curing agent, and a fluoroolefin vinyl ether vinyl ester copolymer resin is used as the thermosetting resin.
固体潤滑剤としては、二硫化モリブデン、二硫化タン
グステン等の硫化物、ポリテトラフルオロエチレン、フ
ッ化黒鉛等のフッ素化合物、黒鉛、シリコーンパウダー
等を用いることができる。これらの固体潤滑剤は1種を
単独で用いても、2種以上を組み合わせても良い。本発
明においては、潤滑耐久性、なじみ性、フィーリング性
に優れることから、硫化物とフッ素化合物と黒鉛の併用
が好ましい。この場合、硫化物とフッ素化合物、黒鉛と
の配合割合は、黒鉛100重量部に対して硫化物10〜1500
重量部、フッ素化合物100〜3000重量部とするのが好ま
しい。As the solid lubricant, sulfides such as molybdenum disulfide and tungsten disulfide, fluorine compounds such as polytetrafluoroethylene and fluorinated graphite, graphite, silicone powder and the like can be used. These solid lubricants may be used alone or in combination of two or more. In the present invention, a combination of a sulfide, a fluorine compound and graphite is preferred because of excellent lubrication durability, conformability, and feeling. In this case, the compounding ratio of sulfide and fluorine compound, graphite, sulfide 10 to 1500 parts by weight of graphite 100 parts by weight
It is preferable to use 100 parts by weight and 3000 parts by weight of a fluorine compound.
固体潤滑剤は、平均粒径が10μm以下、とりわけ5μ
m以下、特に3μm以下のものが好ましい。固体潤滑剤
と樹脂マトリックスとの配合割合は、固体潤滑剤50〜95
重量部、樹脂マトリックス50〜5重量部が好ましく、特
に好ましくは、固体潤滑剤70〜90重量部、樹脂マトリッ
クス30〜10重量部である。Solid lubricants have an average particle size of 10 μm or less, especially 5 μm.
m or less, particularly preferably 3 μm or less. The mixing ratio of the solid lubricant to the resin matrix is 50 to 95 for the solid lubricant.
Parts by weight, preferably 50 to 5 parts by weight of a resin matrix, particularly preferably 70 to 90 parts by weight of a solid lubricant and 30 to 10 parts by weight of a resin matrix.
本発明において、被覆をゴムまたはプラスチックの表
面に設けるには、上記の固体潤滑剤及び熱硬化樹脂並び
に硬化剤を有機溶媒に分散ないしは溶解させて塗布すれ
ば良い。In the present invention, in order to provide the coating on the surface of rubber or plastic, the above-mentioned solid lubricant, thermosetting resin and curing agent may be dispersed or dissolved in an organic solvent and applied.
硬化剤としては、ポリイソシアネート、メラミン樹脂
などを用いることができる。As the curing agent, polyisocyanate, melamine resin, and the like can be used.
有機溶媒としては、メチルエチルケトン、トルエン、
キシレン、イソプロピルアルコール、イソブタノール、
n−ブタノール、酢酸ブチル、MIBK、セロソルブアセテ
ートなどが好適である。Organic solvents include methyl ethyl ketone, toluene,
Xylene, isopropyl alcohol, isobutanol,
Preferred are n-butanol, butyl acetate, MIBK, cellosolve acetate and the like.
塗布する方法としては、刷毛塗りやスプレー掛け、デ
ィッピングなどの各種の方法を採用できる。この塗布を
行なうに先立って、ゴム又はプラスチックの表面を洗浄
したり、あるいは樹脂マトリックスとのなじみを良くす
るための表面処理を施しても良い。このような表面処理
としては、プライマー処理などがあげられる。Various methods such as brushing, spraying, and dipping can be adopted as a method of applying. Prior to performing this coating, the surface of rubber or plastic may be washed, or a surface treatment may be applied to improve compatibility with the resin matrix. Examples of such a surface treatment include a primer treatment.
図面の簡単な説明 第1図は実験方法を説明する概略的な側面図である。
発明を実施するための最良の形態 以下、本発明の実施例及び比較例を説明する。BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a schematic side view illustrating an experimental method.
BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, examples and comparative examples of the present invention will be described.
下記〔比較例1〕〜〔比較例4〕及び〔実施例1〕〜
〔実施例9〕に示す組成物をスプレーすることにより、
ゴム片の表面にスプレーし、各々に示す硬化条件(加熱
条件)にてこの組成物を硬化させ、ゴム片の表面に厚さ
10μmの被覆層を形成した。このゴム片を10mm×6mm×2
mmの大きさに切り出してテストピースとした。このテス
トピースの10mm×6mmの面に上記の被覆層が形成されて
いる。The following [Comparative Example 1] to [Comparative Example 4] and [Example 1] to
By spraying the composition shown in [Example 9]
Spray on the surface of the rubber piece, cure this composition under the respective curing conditions (heating conditions), and apply a thickness to the surface of the rubber piece.
A coating layer of 10 μm was formed. 10mm × 6mm × 2
The test piece was cut out into a size of mm. The above coating layer is formed on a 10 mm × 6 mm surface of this test piece.
このテストピースをFALEX NO.1試験機(Faville−Lev
ally CORPORATION)に装着し、被覆層の耐久性を調べ
た。This test piece is used for FALEX NO.1 tester (Faville-Lev
ally CORPORATION), and the durability of the coating layer was examined.
第1図は、この試験の様子を示す模式的な側面図であ
り、テストピース1はテストピースホルダー2に保持さ
れており、直径35mmのリング3の外周面に荷重9.06kg
(20LBS)にて押し付けられている。リング3の外周面
の材質はSAE4620スチールであり、表面粗さは6〜12rms
である。リング3をその軸心回りに矢印の如く90°の回
動範囲にて100サイクル/minの割合で往復回動させた。FIG. 1 is a schematic side view showing the state of this test. A test piece 1 is held by a test piece holder 2 and a load of 9.06 kg is applied to the outer peripheral surface of a ring 3 having a diameter of 35 mm.
(20LBS). The material of the outer peripheral surface of the ring 3 is SAE4620 steel, and the surface roughness is 6-12 rms
It is. The ring 3 was reciprocated around its axis at a rate of 100 cycles / min in a 90 ° rotation range as shown by the arrow.
この摩擦係数が0.2に達するまでのサイクル数を寿命
サイウルとして測定した。なお、摩擦係数が0.2に達す
る前に被覆層が摩滅し、ゴム層が露出した場合には、そ
の時点までのサイクル数を寿命サイクルとした。The number of cycles until the friction coefficient reached 0.2 was measured as life sioul. When the coating layer was worn out before the coefficient of friction reached 0.2 and the rubber layer was exposed, the number of cycles up to that point was regarded as the life cycle.
各比較例及び実施例の寿命サイクルは表−1の通りで
ある。なお、リング3との摺動を行なう前における各テ
ストピースの被覆層表面の静止摩擦係数と動摩擦係数と
の測定結果を併せて表−1に示す。Table 1 shows the life cycle of each comparative example and example. Table 1 also shows the measurement results of the static friction coefficient and the dynamic friction coefficient of the surface of the coating layer of each test piece before sliding with the ring 3.
この表−1より、本発明の実施例1〜9のテストピー
スは、摩擦係数が小さく、しかも被覆層の耐久性も著し
く高いことが明らかである。From Table 1, it is apparent that the test pieces of Examples 1 to 9 of the present invention have a small coefficient of friction and a remarkably high durability of the coating layer.
以下において用いた固体潤滑剤の平均粒径はいずれも
5μm以下である。Each of the solid lubricants used below has an average particle size of 5 μm or less.
以下において、「部」は「重量部」を意味する。 In the following, “parts” means “parts by weight”.
[比較例1] (ポリウレタン樹脂)ニッポラン5185 100部 (日本ポリウレタン工業(株)) (イソシアネート硬化剤) 10.0部 コロネートHL 硬化条件:80℃〜30分にて [比較例2] (ポリウレタン樹脂) 26.0部 ニッポラン5185 (日本ポリウレタン工業(株)) (二硫化モリブデン) 30.0部 テクニカルグレード (Climax Molybdenum社製) (ポリテトラフルオロエチレン) 42.0部 ルブロンL−5 (ダイキン工業(株)) (グラファイト)ACP1000 2.0部 (日本黒鉛工業(株)) (イソシアネート硬化剤)コロネートHL 2.6部 硬化条件:80℃−30分にて [比較例3](特開昭55−15873号の実施例3に相当) KM−765 45部 (シリコーン分20%エマルジョン) (住越化学(株)) C−PM−4F(触媒 住越化学(株)) 4.5部 二硫化モリブデン(平均粒子径4.5μm) 4.0部 水 52.0部 硬化条件:室温で10分間放置後150℃−10分にて硬化層
を得た。[Comparative Example 1] (Polyurethane resin) Nipporan 5185 100 parts (Nippon Polyurethane Industry Co., Ltd.) (Isocyanate curing agent) 10.0 parts Coronate HL Curing conditions: 80 ° C to 30 minutes [Comparative Example 2] (Polyurethane resin) 26.0 Department Nipporan 5185 (Nippon Polyurethane Industry Co., Ltd.) (Molybdenum disulfide) 30.0 parts Technical grade (Climax Molybdenum) (Polytetrafluoroethylene) 42.0 parts Lubron L-5 (Daikin Industries, Ltd.) (Graphite) ACP1000 2.0 Part (Nippon Graphite Industries Co., Ltd.) (Isocyanate curing agent) Coronate HL 2.6 parts Curing conditions: 80 ° C. for 30 minutes [Comparative Example 3] (corresponding to Example 3 of JP-A-55-15873) 765 45 parts (Silicone content 20% emulsion) (Sumietsu Chemical Co., Ltd.) C-PM-4F (Catalyst Sumitomo Chemical Co., Ltd.) 4.5 parts Molybdenum disulfide (average particle size 4.5 μm) 4.0 parts Water 52 0.0 part Curing conditions: After standing at room temperature for 10 minutes, a cured layer was obtained at 150 ° C. for 10 minutes.
[比較例4] (フルオロオレフィンビニール 100部 エーテルビニールエステル共重合体) フルオネートK702 (大日本インキ化学工業(株)) (イソシアネート硬化剤) 24部 バーノックDN980 (大日本インキ化学工業(株)) 硬化条件:80℃−10分 [実施例1] (フルオロオレフィンビニール 26部 エーテルビニールエステル共重合体) フルオネートK702 (大日本インキ化学工業(株)) (二硫化モリブデン)テクニカルグレード 30部 (Climax Molybdenum社製) (ポリテトラフルオロエチレン) 42部 ルブロンL−5 (ダイキン工業(株)) (グラファイト)ACP1000 2部 (日本黒鉛工業(株)) (イソシアネート硬化剤) 6.2部 バーノックDN980 (大日本インキ化学工業(株)) 硬化条件:80℃−10分 [実施例2] (フルオロオレフィンビニール 28部 エーテルビニールエステル共重合体) フルオネートK702 (大日本インキ化学工業(株)) (二硫化モリブデン)テクニカルグレード 10部 (Climax Molybdenum社製) (ポリテトラフルオロエチレン) 60部 ルブロンL−5 (ダイキン工業(株)) (グラファイト)ACP1000 2部 (日本黒鉛工業(株)) (イソシアネート硬化剤) 6.7部 バーノックDN980 (大日本インキ化学工業(株)) 硬化条件:80℃−10分 [実施例3] (フルオロオレフィンビニール 28部 エーテルビニールエステル共重合体) フルオネートK702 (大日本インキ化学工業(株)) (二硫化モリブデン)テクニカルグレード 47部 (Climax Molybdenum社製) (ポリテトラフルオロエチレン) 23部 ルブロンL−5 (ダイキン工業(株)) (グラファイト)ACP1000 2部 (日本黒鉛工業(株)) (イソシアネート硬化剤) 6.7部 バーノックDN980 (大日本インキ化学工業(株)) 硬化条件:80℃−10分 [実施例4] (フルオロオレフィンビニール 49部 エーテルビニールエステル共重合体) フルオネートK702 (大日本インキ化学工業(株)) (二硫化モリブデン)テクニカルグレード 39部 (ポリテトラフルオロエチレン) 10部 ルブロンL−5 (グラファイト)ACP1000 2部 (イソシアネート硬化剤) 6.7部 バーノックDN980 硬化条件:80℃−10分 [実施例5] (フルオロオレフィンビニール 49部 エーテルビニールエステル共重合体) フルオネートK702 (二硫化モリブデン)テクニカルグレード 47部 (ポリテトラフルオロエチレン) 2.5部 ルブロンL−5 (グラファイト)ACP1000 1.5部 (イソシアネート硬化剤) 12.0部 バーノックDN980 硬化条件:80℃−10分 [実施例6] (フルオロオレフィンビニール 49部 エーテルビニールエステル共重合体) フルオネートK702 (二硫化モリブデン)テクニカルグレード 49部 (グラファイト)ACP1000 2部 (イソシアネート硬化剤) 12部 バーノックDN980 硬化条件:80℃−10分 [実施例7] (フルオロオレフィンビニール 39部 エーテルビニールエステル共重合体) フルオネートK702 (二硫化モリブデン)テクニカルグレード 59部 (グラファイト)ACP1000 2部 (イソシアネート硬化剤) 9.4部 バーノックDN980 硬化条件:80℃−10分 [実施例8] (フルオロオレフィンビニール 28部 エーテルビニールエステル共重合体) フルオネートK702 (二硫化モリブデン)テクニカルグレード 70部 (グラファイト)ACP1000 2部 (イソシアネート硬化剤) 6.7部 バーノックDN980 硬化条件:80℃−10分 [実施例9] (フルオロオレフィンビニール 20部 エーテルビニールエステル共重合体) フルオネートK702 (二硫化モリブデン)テクニカルグレード 78部 (グラファイト)ACP1000 2部 (イソシアネート硬化剤) 4.8部 バーノックDN980 硬化条件:80℃−10分 産業上の利用可能性 以上の通り、本発明の表面被覆部材は、その被覆面の
摩擦係数がきわめて小さく、しかも被覆層の耐久性が著
しく高い。[Comparative Example 4] (fluoroolefin vinyl 100 parts ether vinyl ester copolymer) Fluonate K702 (Dainippon Ink and Chemicals, Inc.) (isocyanate curing agent) 24 parts Burnock DN980 (Dainippon Ink and Chemicals, Inc.) Conditions: 80 ° C. for 10 minutes [Example 1] (Fluoroolefin vinyl 26 parts ether vinyl ester copolymer) Fluonate K702 (Dainippon Ink Chemical Industry Co., Ltd.) (molybdenum disulfide) Technical grade 30 parts (Climax Molybdenum) (Polytetrafluoroethylene) 42 parts Lubron L-5 (Daikin Industries, Ltd.) (Graphite) ACP1000 2 parts (Nippon Graphite Industries, Ltd.) (Isocyanate curing agent) 6.2 parts Burnock DN980 (Dainippon Ink and Chemicals) Curing conditions: 80 ° C. for 10 minutes [Example 2] (28 parts of fluoroolefin vinyl) -Ter vinyl ester copolymer) Fluonate K702 (Dainippon Ink & Chemicals, Inc.) (molybdenum disulfide) Technical grade 10 parts (Climax Molybdenum) (polytetrafluoroethylene) 60 parts Lubron L-5 (Daikin Industries) (Graphite) ACP1000 2 parts (Nippon Graphite Industry Co., Ltd.) (Isocyanate curing agent) 6.7 parts Burnock DN980 (Dainippon Ink and Chemicals, Inc.) Curing conditions: 80 ° C. for 10 minutes [Example 3] (Fluoroolefin vinyl 28 parts ether vinyl ester copolymer) Fluonate K702 (Dainippon Ink & Chemicals, Inc.) (molybdenum disulfide) technical grade 47 parts (Climax Molybdenum) (polytetrafluoroethylene) 23 parts Lubron L -5 (Daikin Industries, Ltd.) (Graphite) ACP1000 2nd Part (Nippon Graphite Industries, Ltd.) ( 6.7 parts Barnock DN980 (Dainippon Ink & Chemicals, Inc.) Curing conditions: 80 ° C-10 minutes [Example 4] (Fluoroolefin vinyl 49 parts ether vinyl ester copolymer) Fluonate K702 (Dainippon Ink) Chemical Industry Co., Ltd. (Molybdenum disulfide) Technical grade 39 parts (Polytetrafluoroethylene) 10 parts Lubron L-5 (graphite) ACP1000 2 parts (Isocyanate curing agent) 6.7 parts Burnock DN980 Curing conditions: 80 ° C-10 minutes [Example 5] (fluoroolefin vinyl 49 parts ether vinyl ester copolymer) Fluonate K702 (molybdenum disulfide) technical grade 47 parts (polytetrafluoroethylene) 2.5 parts Lubron L-5 (graphite) ACP1000 1.5 parts (isocyanate cured 12.0 parts Burnock DN980 Curing condition: 80 ℃ -1 0 minutes [Example 6] (fluoroolefin vinyl 49 parts ether vinyl ester copolymer) Fluonate K702 (molybdenum disulfide) technical grade 49 parts (graphite) ACP1000 2 parts (isocyanate curing agent) 12 parts Burnock DN980 Curing conditions: 80 C-10 minutes [Example 7] (fluoroolefin vinyl 39 parts ether vinyl ester copolymer) Fluonate K702 (molybdenum disulfide) technical grade 59 parts (graphite) ACP1000 2 parts (isocyanate curing agent) 9.4 parts Barnock DN980 Curing conditions : 80 ° C-10 minutes [Example 8] (Fluoroolefin vinyl 28 parts Ether vinyl ester copolymer) Fluonate K702 (Molybdenum disulfide) Technical grade 70 parts (Graphite) ACP1000 2 parts (Isocyanate curing agent) 6.7 parts Barnock DN980 Hardening strip Case: 80 ° C. for 10 minutes [Example 9] (Fluoroolefin vinyl 20 parts Ether vinyl ester copolymer) Fluonate K702 (Molybdenum disulfide) Technical grade 78 parts (Graphite) ACP1000 2 parts (Isocyanate curing agent) 4.8 parts DN980 Curing condition: 80 ℃ -10min INDUSTRIAL APPLICABILITY As described above, the surface-coated member of the present invention has a very low coefficient of friction on the coated surface, and the coating layer has extremely high durability.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI C10N 50:08 (58)調査した分野(Int.Cl.6,DB名) C08J 5/00 - 5/02 C08J 5/12 - 5/22 C10M 107/38 C08J 7/04 ──────────────────────────────────────────────────の Continued on the front page (51) Int.Cl. 6 identification code FI C10N 50:08 (58) Fields surveyed (Int.Cl. 6 , DB name) C08J 5/00-5/02 C08J 5/12 -5/22 C10M 107/38 C08J 7/04
Claims (12)
なる被覆層が表面に形成されている表面被覆部材であっ
て、該樹脂マトリックスは硬化剤によって硬化された熱
硬化樹脂であり、該熱硬化樹脂がフルオロオレフィンビ
ニールエーテルビニールエステル共重合体樹脂であるこ
とを特徴とする表面被覆部材。1. A surface-coated member having a coating layer comprising a solid lubricant and a resin matrix formed on a surface thereof, wherein the resin matrix is a thermosetting resin cured by a curing agent, A surface covering member, wherein the resin is a fluoroolefin vinyl ether vinyl ester copolymer resin.
及びシリコーンパウダーの1種又は2種以上である請求
項1の表面被覆部材。2. The surface-coated member according to claim 1, wherein the solid lubricant is one or more of sulfide, fluorine compound, graphite and silicone powder.
合が、固体潤滑剤50〜95重量部、樹脂マトリックス50〜
5重量部である請求項1又は2の表面被覆部材。3. The mixing ratio of the solid lubricant and the resin matrix is 50 to 95 parts by weight of the solid lubricant and 50 to 95 parts by weight of the resin matrix.
3. The surface covering member according to claim 1, wherein the amount is 5 parts by weight.
合が、固体潤滑剤70〜90重量部、樹脂マトリックス30〜
10重量部である請求項1又は2の表面被覆摺動部材。4. The mixing ratio of the solid lubricant and the resin matrix is 70 to 90 parts by weight of the solid lubricant and 30 to 90 parts by weight of the resin matrix.
3. The surface-coated sliding member according to claim 1, wherein the amount is 10 parts by weight.
化タングステンである請求項2ないし4のいずれか1項
の表面被覆部材。5. The surface covering member according to claim 2, wherein the sulfide is molybdenum disulfide and / or tungsten disulfide.
ン及び/又はフッ化黒鉛である請求項2ないし5のいず
れか1項の表面被覆部材。6. The surface covering member according to claim 2, wherein the fluorine compound is polytetrafluoroethylene and / or graphite fluoride.
鉛よりなりその配合割合は、黒鉛100重量部に対し、硫
化物10〜1500重量部、フッ素化合物100〜3000重量部で
ある請求項2ないし6のいずれか1項の表面被覆部材。7. A solid lubricant comprising a sulfide, a fluorine compound and graphite in a compounding ratio of 10 to 1500 parts by weight of sulfide and 100 to 3000 parts by weight of a fluorine compound per 100 parts by weight of graphite. 7. The surface-coated member according to any one of items 6 to 6.
請求項2ないし7のいずれか1項の表面被覆摺動部材。8. The surface-coated sliding member according to claim 2, wherein the fixed lubricant has an average particle size of 10 μm or less.
請求項2ないし7のいずれか1項の表面被覆摺動部材。9. The surface-coated sliding member according to claim 2, wherein the fixed lubricant has an average particle size of 5 μm or less.
る請求項2ないし7のいずれか1項の表面被覆摺動部
材。10. The surface-coated sliding member according to claim 2, wherein the fixed lubricant has an average particle size of 3 μm or less.
ある請求項1ないし10のいずれか1項の表面被覆摺動部
材。11. The surface-coated sliding member according to claim 1, wherein the surface-coated member is a wiper blade rubber.
求項1ないし10のいずれか1項の表面被覆摺動部材。12. The surface-coated sliding member according to claim 1, wherein the surface-coated member is a seal packing.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/JP1991/000533 WO1992018560A1 (en) | 1991-04-22 | 1991-04-22 | Surface-coated member |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2903709B2 true JP2903709B2 (en) | 1999-06-14 |
Family
ID=14014376
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3507549A Expired - Fee Related JP2903709B2 (en) | 1991-04-22 | 1991-04-22 | Surface coating member |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2903709B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010042674A (en) * | 2008-08-12 | 2010-02-25 | Xerox Corp | Opening plate coated with coating composition, process for applying coating composition to opening plate, and coating composition |
WO2011021725A1 (en) * | 2009-08-21 | 2011-02-24 | 東レ・ダウコーニング株式会社 | Coating composition for sliding members |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59103022A (en) * | 1982-12-03 | 1984-06-14 | Daido Metal Kogyo Kk | Bearing material having superior wearing resistance |
JPS61266451A (en) * | 1985-05-21 | 1986-11-26 | Daido Metal Kogyo Kk | Composition for sliding member |
-
1991
- 1991-04-22 JP JP3507549A patent/JP2903709B2/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59103022A (en) * | 1982-12-03 | 1984-06-14 | Daido Metal Kogyo Kk | Bearing material having superior wearing resistance |
JPS61266451A (en) * | 1985-05-21 | 1986-11-26 | Daido Metal Kogyo Kk | Composition for sliding member |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010042674A (en) * | 2008-08-12 | 2010-02-25 | Xerox Corp | Opening plate coated with coating composition, process for applying coating composition to opening plate, and coating composition |
WO2011021725A1 (en) * | 2009-08-21 | 2011-02-24 | 東レ・ダウコーニング株式会社 | Coating composition for sliding members |
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