JPH04345667A - Sliding material - Google Patents
Sliding materialInfo
- Publication number
- JPH04345667A JPH04345667A JP11822991A JP11822991A JPH04345667A JP H04345667 A JPH04345667 A JP H04345667A JP 11822991 A JP11822991 A JP 11822991A JP 11822991 A JP11822991 A JP 11822991A JP H04345667 A JPH04345667 A JP H04345667A
- Authority
- JP
- Japan
- Prior art keywords
- powder
- resin
- bearing
- wear
- sliding material
- 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
Links
- 239000000463 material Substances 0.000 title claims abstract description 14
- 239000000843 powder Substances 0.000 claims abstract description 27
- 229920001343 polytetrafluoroethylene Polymers 0.000 claims abstract description 18
- 239000004810 polytetrafluoroethylene Substances 0.000 claims abstract description 18
- -1 polytetrafluoroethylene Polymers 0.000 claims abstract description 6
- 229920003002 synthetic resin Polymers 0.000 claims abstract description 6
- 239000000057 synthetic resin Substances 0.000 claims abstract description 6
- 229920005989 resin Polymers 0.000 claims description 19
- 239000011347 resin Substances 0.000 claims description 19
- 238000004898 kneading Methods 0.000 claims description 7
- WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical compound [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 claims description 6
- 238000002347 injection Methods 0.000 claims description 3
- 239000007924 injection Substances 0.000 claims description 3
- 239000004734 Polyphenylene sulfide Substances 0.000 abstract description 6
- 229920000069 polyphenylene sulfide Polymers 0.000 abstract description 6
- 238000002156 mixing Methods 0.000 abstract description 3
- 238000005299 abrasion Methods 0.000 abstract 1
- 238000010586 diagram Methods 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 7
- 230000007423 decrease Effects 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 229910001111 Fine metal Inorganic materials 0.000 description 3
- 239000002131 composite material Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 229910000906 Bronze Inorganic materials 0.000 description 1
- 229910000975 Carbon steel Inorganic materials 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 229920013633 Fortron Polymers 0.000 description 1
- 239000004738 Fortron® Substances 0.000 description 1
- 229930182556 Polyacetal Natural products 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000010974 bronze Substances 0.000 description 1
- 239000010962 carbon steel Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 229920006351 engineering plastic Polymers 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 230000013011 mating Effects 0.000 description 1
- 239000002905 metal composite material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 238000005453 pelletization Methods 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 239000009719 polyimide resin Substances 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 238000005204 segregation Methods 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
Landscapes
- Sliding-Contact Bearings (AREA)
- Lubricants (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は摺動材料に関し、特に射
出成形可能な金属系微粉未含有摺動材料に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a sliding material, and more particularly to an injection moldable sliding material containing no metallic fine powder.
【0002】0002
【従来の技術】従来、樹脂一体型軸受の欠点である機械
的強度、寸法安定性、熱伝導性などを改善するために複
合型軸受が用いられている。この複合型軸受としては複
数の金属成分、無機化合物等から成る金属系複合型軸受
または金属成分と合成樹脂成分等から成る合成樹脂系複
合型軸受が知られている。2. Description of the Related Art Conventionally, composite bearings have been used to improve mechanical strength, dimensional stability, thermal conductivity, etc., which are disadvantages of resin-integrated bearings. As this composite type bearing, a metal composite type bearing made of a plurality of metal components, inorganic compounds, etc., and a synthetic resin type composite type bearing made of a metal component, a synthetic resin component, etc. are known.
【0003】0003
【発明が解決しようとする課題】しかし、前記金属系微
粉末を混入した軸受は成形工程で焼結を必要とし、また
、多数の工程と、その工程の中には複雑な処理が必要な
場合もある。そのため軸受の製造コストが高くなる。
そこで本発明の目的は量産可能であり、かつ耐摩耗性で
低摩擦係数の金属系微粉末混入軸受を提供することであ
る。[Problems to be Solved by the Invention] However, bearings containing fine metal powders require sintering in the forming process, and may require multiple processes and complex treatments in some of the processes. There is also. This increases the manufacturing cost of the bearing. SUMMARY OF THE INVENTION Therefore, an object of the present invention is to provide a bearing containing fine metal powder that can be mass-produced, has wear resistance, and has a low coefficient of friction.
【0004】0004
【課題を解決するための手段】本発明の上記目的は、合
成樹脂をベースレジンとして用い、これに対し20〜4
0重量%の鉛微粉末および20〜40重量%のポリテト
ラフロロエチレン粉末を加えて混練し、射出成形可能と
した摺動材料により達成される。[Means for Solving the Problems] The above object of the present invention is to use a synthetic resin as a base resin,
This is achieved by adding and kneading 0% by weight of lead fine powder and 20 to 40% by weight of polytetrafluoroethylene powder to make the sliding material moldable by injection molding.
【0005】1)ベースレジン
合成樹脂を本発明のベースレジンとして、摺動材料成分
の結合剤として用いる。成形時の生産性を優先するなら
ば熱可塑性の樹脂が望ましい。また摺動材料として高い
限界PV値を達成するためには、耐熱性に優れたいわゆ
るエンジニアリングプラスチックを用いることが望まし
い。具体的にはポリアセタール、ポリアミド、ポリフェ
ニレンサルファイド、液晶ポリエステル、ポリエーテル
ニトリルなどの樹脂を用いることができる。ポリフェニ
レンサルファイド(PPS)樹脂は機械的強度と耐熱性
に優れた樹脂であり、コストパフォーマンス的に最適で
ある。しかも、この樹脂は、混練時または成形時に鉛微
粉末を酸化させたり、樹脂自身が分解したりすることが
ない。さらに、この中でも直鎖形のPPS樹脂の方が架
橋形のものに比べ若干ながら摺動特性が良好で、かつウ
ェルド強度も有利であり、また添加剤を多量に含有でき
る。また、より高い耐熱性や耐クリープ性等を要求され
る場合には熱硬化性の樹脂をベースとして用いることが
できる。具体的にはフェノール樹脂、エポキシポリイミ
ド樹脂等である。1) Base Resin A synthetic resin is used as the base resin of the present invention and as a binder for sliding material components. If priority is given to productivity during molding, thermoplastic resin is desirable. Furthermore, in order to achieve a high limit PV value as a sliding material, it is desirable to use so-called engineering plastics that have excellent heat resistance. Specifically, resins such as polyacetal, polyamide, polyphenylene sulfide, liquid crystal polyester, and polyether nitrile can be used. Polyphenylene sulfide (PPS) resin is a resin with excellent mechanical strength and heat resistance, and is optimal in terms of cost performance. Moreover, this resin does not oxidize fine lead powder during kneading or molding, nor does the resin itself decompose. Furthermore, among these, linear PPS resins have slightly better sliding properties and weld strength than crosslinked ones, and can contain a large amount of additives. Furthermore, if higher heat resistance, creep resistance, etc. are required, a thermosetting resin can be used as the base. Specifically, phenol resin, epoxy polyimide resin, etc. are used.
【0006】2)鉛粉末
鉛(Pb)粉末は純度97%以上で200メッシュ(粒
子径75μm以下)程度のものが望ましい。製造法とし
てはアトマイズ法によるものが粋砕品と比べ、コンパウ
ンド時に酸化変質しにくく、また安価であるので望まし
い。また、鉛粉末の含有割合が20重量%未満であると
、摺動材料の耐摩耗性が低下し、また40重量%を超え
ると分散性が低下し、例えばタンブラー形ミキサーでは
均一に混合することができなくなり、成形品に偏析を生
じさせる。このとき、同時にPTFEの含有率が低下し
、摩擦係数が上昇する。鉛粉末は望ましくは30重量%
で用いられる。2) Lead Powder The lead (Pb) powder preferably has a purity of 97% or more and a size of about 200 mesh (particle size of 75 μm or less). As for the manufacturing method, the atomization method is preferable because it is less susceptible to oxidative deterioration during compounding and is less expensive than crushed products. Furthermore, if the lead powder content is less than 20% by weight, the wear resistance of the sliding material will decrease, and if it exceeds 40% by weight, the dispersibility will decrease, making it difficult to mix uniformly with a tumbler mixer, for example. This results in segregation in the molded product. At this time, the content of PTFE simultaneously decreases and the coefficient of friction increases. Lead powder is preferably 30% by weight
used in
【0007】3)ポリテトラフロロエチレンベースレジ
ンは潤滑性能が劣るので、潤滑性改善剤としてポリテト
ラフロロエチレン(PTFE)粉末を用いる。PTFE
樹脂は低分子量のものを用い、粒子径は0.2〜0.3
μmであり、凝集状態では径が5〜8μmになるものが
望ましい。またポリテトラフロロエチレン(PTFE)
粉末の配合割合が20重量%未満であると、耐摩耗性が
低下し、また40重量%を超えると成形品が著しく脆く
なり、実用に耐えない。PTFEは望ましくは30重量
%で用いられる。3) Polytetrafluoroethylene (PTFE) powder is used as a lubricity improving agent because polytetrafluoroethylene base resin has poor lubricity. PTFE
The resin used is of low molecular weight, and the particle size is 0.2 to 0.3.
[mu]m, and preferably has a diameter of 5 to 8 [mu]m in the agglomerated state. Also polytetrafluoroethylene (PTFE)
If the blending ratio of powder is less than 20% by weight, wear resistance will decrease, and if it exceeds 40% by weight, the molded product will become extremely brittle and cannot be put into practical use. PTFE is preferably used at 30% by weight.
【0008】[0008]
【作用】ベースレジンの粉末とPTFE粉およびPb粉
を、例えばタンブラ形ミキサーに投入し、約10分間程
度撹拌混合する。これによってPTFE粉が静電気を発
生し、ベースレジンの粒子の外表面に均一に付着する。
さらにPbの微粉末がPTFEに取り囲まれる形でベー
ス樹脂の表面に均一に付着する。このようにして、極め
て比重の異なる粉末同志でも均一に混合する。この状態
のものを2軸混練装置に投入し、ペレットを製造する。
混練温度は310℃±10℃が望ましく、これ以上にな
るとPb粉が溶解し凝集してしまう。[Operation] The base resin powder, PTFE powder and Pb powder are placed in, for example, a tumbler type mixer, and mixed by stirring for about 10 minutes. This causes the PTFE powder to generate static electricity and adhere uniformly to the outer surface of the base resin particles. Further, fine Pb powder is uniformly attached to the surface of the base resin in a form surrounded by PTFE. In this way, even powders having extremely different specific gravities can be mixed uniformly. The material in this state is put into a twin-screw kneading device to produce pellets. The kneading temperature is preferably 310°C±10°C; if it exceeds this temperature, the Pb powder will dissolve and aggregate.
【0009】[0009]
【実施例】ベースレジンとして本実施例では呉羽化学工
業(株)のポリフェニレンサルファイドであるフォート
ロン(商標名)の中でW−214グレードを用いた。ま
た、PTFE樹脂粉として本実施例ではダイキン工業(
株)のルブロンL−5(商標名)を用いた。Pb粉は本
実施例では福田金属箔粉工業(株)のPb−At−20
0(商標名)を用いた。ベースレジン粉末70WT%と
PTFE樹脂粉30WT%およびPb粉30WT%をタ
ンブラ形ミキサーに投入し、約10分間程度撹拌混合さ
せ、2軸混練装置に投入し、ペレットを製造する。混練
温度は310℃±10℃になるように調節した。[Example] In this example, W-214 grade of Fortron (trade name), a polyphenylene sulfide manufactured by Kureha Chemical Industry Co., Ltd., was used as the base resin. In addition, in this example, Daikin Industries (
Rubron L-5 (trade name) manufactured by Co., Ltd. was used. In this example, the Pb powder was Pb-At-20 manufactured by Fukuda Metal Foil and Powder Industry Co., Ltd.
0 (trade name) was used. 70 WT% of base resin powder, 30 WT% of PTFE resin powder, and 30 WT% of Pb powder are placed in a tumbler type mixer, stirred and mixed for about 10 minutes, and then placed in a twin-screw kneading device to produce pellets. The kneading temperature was adjusted to 310°C±10°C.
【0010】前記各成分の配合率は次の表1に示す。比
較例として、鉛粉の含有量とPTFE樹脂粉の含有量を
それぞれ変化させたものを用いた。そして、表1に示す
摩耗係数と摩擦係数を持つ摺動材料が得られた(製造直
後の数値)。[0010] The blending ratio of each of the above components is shown in Table 1 below. As comparative examples, samples were used in which the content of lead powder and the content of PTFE resin powder were varied. A sliding material having the wear coefficient and friction coefficient shown in Table 1 was obtained (values immediately after manufacture).
【0011】[0011]
【表1】[Table 1]
【0012】次に実施例1〜3と比較例1、2の摺動材
料を日精樹脂工業(株)製のPS60型射出成形機を用
いて軸受を常法通り作製して、次の試験条件で摩擦係数
と摩耗寸法と軸受温度の経時変化を試験した。
試験機 :ジャーナル型軸受試験機滑り速度
:25m/min
面圧 :15kgf/cm2雰囲気温度:2
3℃±1℃
潤滑条件 :完全無給油
相手軸 :機械構造用炭素鋼(S45C)Next, bearings were manufactured from the sliding materials of Examples 1 to 3 and Comparative Examples 1 and 2 using a PS60 injection molding machine manufactured by Nissei Jushi Kogyo Co., Ltd. in a conventional manner, and the bearings were subjected to the following test conditions. The friction coefficient, wear dimensions, and bearing temperature changes over time were tested. Testing machine: Journal type bearing testing machine sliding speed
: 25m/min Surface pressure: 15kgf/cm2 Atmosphere temperature: 2
3℃±1℃ Lubrication conditions: Completely oil-free Mating shaft: Carbon steel for machine structure (S45C)
【00
13】P(面圧)とV(速度)を一定にして測定して経
時変化を見た結果を図1〜図7に示し、そのまとめを図
8に示す。本実施例1〜3においては摩擦係数は長時間
の使用にも安定した値を示し、摩耗寸法の変化率も比較
的緩やかである。特に最適組成を持つ本発明の実施例で
ある実施例1の場合の摩耗寸法は0.05μm/時間で
あり、特に好ましい性能を示している。一方、比較例の
ものは初期摩耗が大きい。00
13] Figures 1 to 7 show the results of measuring changes over time while keeping P (surface pressure) and V (velocity) constant, and a summary is shown in Figure 8. In Examples 1 to 3, the coefficient of friction shows a stable value even after long-term use, and the rate of change in wear dimension is relatively slow. In particular, in the case of Example 1, which is an example of the present invention having an optimum composition, the wear dimension was 0.05 μm/hour, showing particularly favorable performance. On the other hand, the comparative example had large initial wear.
【0014】前記試験データはPV値を一定にして摺動
特性を見たものであるが、限界PV値を測定した結果を
図9に示す。同図から明らかなように本実施例の軸受が
優れていることがより明確になった。[0014] The above test data was obtained by looking at the sliding characteristics while keeping the PV value constant, and the results of measuring the limit PV value are shown in FIG. As is clear from the figure, it has become clearer that the bearing of this example is superior.
【0015】なお、同一条件での鋼裏金に青銅焼結層を
形成させ、その焼結層の上にPTFEとPbの層を形成
させた従来の複層軸受(市販DUドライ軸受)の摩擦係
数と摩耗寸法の経時変化を図10に示す。Furthermore, under the same conditions, the friction coefficient of a conventional multilayer bearing (commercially available DU dry bearing) in which a bronze sintered layer is formed on a steel backing metal, and a layer of PTFE and Pb is formed on the sintered layer. Figure 10 shows the changes in wear dimensions over time.
【0016】本実施例の摺動材料により製造された軸受
はPb粉末が相手材(軸)の表面へ付着し、引き延ばさ
れ相手の表面を平滑にすることにより、摺動面積を大き
く(面圧が低下)する効果およびPTFE粉末の摩耗を
防止する効果を有する。またPb粉末自体固体潤滑剤と
しても作用することは周知の通りである。The bearing manufactured using the sliding material of this example has a large sliding area ( This has the effect of reducing surface pressure) and preventing wear of the PTFE powder. Furthermore, it is well known that Pb powder itself also acts as a solid lubricant.
【0017】[0017]
【発明の効果】本発明の摺動材料から得られる軸受は経
時変化のない安定した摩擦係数を持ち、摩擦寸法もほと
んど長期使用の後もほとんど変わらず、現存の金属系微
粉末の軸受と比較して非常に優れた性能を有する。また
、コンパウドをペレット化することにより射出成形可能
とし量産することができる特徴もある。[Effects of the Invention] The bearing obtained from the sliding material of the present invention has a stable coefficient of friction that does not change over time, and the friction dimension hardly changes even after long-term use, compared with existing bearings made of fine metal powder. It has very good performance. Another feature is that by pelletizing the compound, it can be injection molded and mass-produced.
【図1】本発明の実施例1の摩擦係数の経時変化を示す
図である。FIG. 1 is a diagram showing changes over time in the friction coefficient of Example 1 of the present invention.
【図2】本発明の実施例1の摩耗寸法の経時変化を示す
図である。FIG. 2 is a diagram showing changes over time in wear dimensions in Example 1 of the present invention.
【図3】本発明の実施例1の軸受温度の経時変化を示す
図である。FIG. 3 is a diagram showing changes in bearing temperature over time in Example 1 of the present invention.
【図4】実施例2の摩擦係数、摩耗寸法、軸受温度の経
時変化を示す図である。FIG. 4 is a diagram showing changes over time in friction coefficient, wear size, and bearing temperature in Example 2.
【図5】実施例3の摩擦係数、摩耗寸法、軸受温度の経
時変化を示す図である。FIG. 5 is a diagram showing changes over time in friction coefficient, wear size, and bearing temperature in Example 3.
【図6】比較例1の摩擦係数、摩耗寸法、軸受温度の経
時変化を示す図である。FIG. 6 is a diagram showing changes in friction coefficient, wear size, and bearing temperature over time in Comparative Example 1.
【図7】比較例2の摩擦係数、摩耗寸法、軸受温度の経
時変化を示す図である。FIG. 7 is a diagram showing changes over time in the friction coefficient, wear size, and bearing temperature of Comparative Example 2.
【図8】本発明の前記実施例と比較例の一定PV値での
平均摩擦係数と摩耗寸法の変化速度を示す図である。FIG. 8 is a diagram showing the average coefficient of friction and the rate of change in wear dimension at a constant PV value for the embodiments of the present invention and comparative examples.
【図9】本発明の前記実施例と比較例の限界PV値を示
す図である。FIG. 9 is a diagram showing the limit PV values of the embodiments of the present invention and comparative examples.
【図10】従来の複層軸受の摩擦係数と摩耗寸法の経時
変化を示す図である。FIG. 10 is a diagram showing changes over time in the friction coefficient and wear size of a conventional multilayer bearing.
Claims (1)
これに対し20〜40重量%の鉛微粉末および20〜4
0重量%のポリテトラフロロエチレン粉末を加えて混練
し、射出成形可能としたことを特徴とする摺動材料。[Claim 1] Using a synthetic resin as a base resin,
On the other hand, 20-40% by weight of fine lead powder and 20-40% by weight
A sliding material characterized by being made injection moldable by adding and kneading 0% by weight of polytetrafluoroethylene powder.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11822991A JP3018559B2 (en) | 1991-05-23 | 1991-05-23 | Sliding material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11822991A JP3018559B2 (en) | 1991-05-23 | 1991-05-23 | Sliding material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04345667A true JPH04345667A (en) | 1992-12-01 |
JP3018559B2 JP3018559B2 (en) | 2000-03-13 |
Family
ID=14731425
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11822991A Expired - Fee Related JP3018559B2 (en) | 1991-05-23 | 1991-05-23 | Sliding material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3018559B2 (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06327873A (en) * | 1993-05-26 | 1994-11-29 | Hirose Mfg Co Ltd | Hook retainer in final sewing machine |
JPH07664A (en) * | 1993-06-14 | 1995-01-06 | Hirose Mfg Co Ltd | Sewing machine part |
JPH07144082A (en) * | 1993-11-22 | 1995-06-06 | Hirose Mfg Co Ltd | Fully rotary bobbin |
JPH07231992A (en) * | 1994-02-24 | 1995-09-05 | Hirose Mfg Co Ltd | Full-rotating bobbin case |
US5651323A (en) * | 1994-02-24 | 1997-07-29 | Hirose Manufacturing Co., Ltd. | Hook assembly with coated surfaces for sewing machine |
CN100443754C (en) * | 2004-09-01 | 2008-12-17 | Ntn株式会社 | Shaft member for hydrodynamic bearing device |
-
1991
- 1991-05-23 JP JP11822991A patent/JP3018559B2/en not_active Expired - Fee Related
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06327873A (en) * | 1993-05-26 | 1994-11-29 | Hirose Mfg Co Ltd | Hook retainer in final sewing machine |
JPH07664A (en) * | 1993-06-14 | 1995-01-06 | Hirose Mfg Co Ltd | Sewing machine part |
JPH07144082A (en) * | 1993-11-22 | 1995-06-06 | Hirose Mfg Co Ltd | Fully rotary bobbin |
JPH07231992A (en) * | 1994-02-24 | 1995-09-05 | Hirose Mfg Co Ltd | Full-rotating bobbin case |
US5651323A (en) * | 1994-02-24 | 1997-07-29 | Hirose Manufacturing Co., Ltd. | Hook assembly with coated surfaces for sewing machine |
CN100443754C (en) * | 2004-09-01 | 2008-12-17 | Ntn株式会社 | Shaft member for hydrodynamic bearing device |
Also Published As
Publication number | Publication date |
---|---|
JP3018559B2 (en) | 2000-03-13 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
LAPS | Cancellation because of no payment of annual fees |