JPH02219895A - Composition for sliding member material - Google Patents
Composition for sliding member materialInfo
- Publication number
- JPH02219895A JPH02219895A JP4276889A JP4276889A JPH02219895A JP H02219895 A JPH02219895 A JP H02219895A JP 4276889 A JP4276889 A JP 4276889A JP 4276889 A JP4276889 A JP 4276889A JP H02219895 A JPH02219895 A JP H02219895A
- Authority
- JP
- Japan
- Prior art keywords
- carbon fiber
- tetrafluoroethylene resin
- powder
- wear
- composition
- 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
Landscapes
- Sliding-Contact Bearings (AREA)
- Lubricants (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
この発明は、機械的要素に不可欠の摺動部材料用組成物
に関するものである。DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to a composition for a sliding part material essential for mechanical elements.
〔従来の技術]
四フッ化エチレン樹脂は、耐熱性、耐薬品性、摺動特性
などにすぐれているので、シール材として広く用いられ
ているが1、この樹脂単独では外力による変形量が大き
く、また摩耗量も大きいので、各種の充填材を配合して
これら欠点を改善しようとする試みがなされている。た
とえば、充填材としてはガラス繊維、炭素繊維、金属粉
末などが用いられているが、近年は苛酷な条件下での使
用検討が増加し、従来のものでは限界PV値(ここでP
V値は軸受特性を表すのに用いられ、軸受材の相互比較
の目安となるものであり、圧力Pと摺動面速度Vとの関
数で表わされ、この値が高いほど耐圧性、耐速度性にす
ぐれていることになる)が低いため、このような要求に
対して対応できなくなって来ている。また摺動部用材料
の相手材が、最近の軽量化傾向に伴ってアルミニウムが
利用される場合が増えているが、従来の摺動部用材料で
は相手のアルミニウム材を摩耗させるので、使用に際し
ては幾多の困難があった。[Conventional technology] Tetrafluoroethylene resin has excellent heat resistance, chemical resistance, and sliding properties, so it is widely used as a sealing material1. However, when using this resin alone, the amount of deformation due to external force is large. Also, since the amount of wear is large, attempts have been made to improve these drawbacks by adding various fillers. For example, glass fiber, carbon fiber, metal powder, etc. are used as fillers, but in recent years there has been an increase in consideration of their use under harsh conditions, and conventional fillers have limited PV values (here, P
The V value is used to express bearing characteristics and serves as a guideline for mutual comparison of bearing materials.It is expressed as a function of pressure P and sliding surface speed V, and the higher this value, the better the pressure resistance and durability. However, due to the low speed (which means that it has excellent speed), it has become impossible to meet such demands. In addition, aluminum is increasingly being used as a mating material for sliding parts due to the recent trend toward weight reduction, but conventional materials for sliding parts wear out the mating aluminum material, so it is difficult to use when using it. There were many difficulties.
このように、従来の技術においては、限界PV値が高く
、しかもアルミニウムのような軟質相手材を殆んど摩耗
させないで、近年特に苛酷になって来た使用条件下にお
いそ充分に耐え得る摺動特性を有する摺動部材料用組成
物は得られていないという問題点があり、これを解決す
ることが課題であった。In this way, conventional technology has been able to create a slide that has a high limit PV value, hardly wears out soft mating materials such as aluminum, and can withstand the usage conditions that have become particularly severe in recent years. There is a problem in that a composition for a sliding part material having dynamic properties has not been obtained, and it has been an issue to solve this problem.
〔課題を解決するための手段]
上記の11Bを解決するために、この発明は平均繊維径
が1〜20−でかつアスペクト比が1〜50である炭素
m112〜30重量%と、平均粒径が0.5〜40JI
−であるカルシウム化合物粉末035〜50重量%とを
必須成分として含有し、残部が四フッ化エチレン樹脂か
らなる摺動部材料用組成物とする手段を採用したもので
ある。以下その詳細を述べる。[Means for Solving the Problems] In order to solve the above problem 11B, the present invention uses 112 to 30% by weight of carbon having an average fiber diameter of 1 to 20 and an aspect ratio of 1 to 50, and an average particle diameter of 112 to 30% by weight. is 0.5~40JI
- 035 to 50% by weight of calcium compound powder as an essential component, and the remainder is tetrafluoroethylene resin. The details will be described below.
まず、この発明における四フッ化エチレン樹脂(以下P
TFEと略記する)は四フッ化エチレンの単独重合体で
あって、伊国モンテジソン社製:アルゴフロン、米国デ
ュポン社製:テフロン、英国アイ・シー・アイ社&!=
フルオン、ダイキン工業社製:ポリフロン等それぞれの
登録商標名で市販されているフッ素樹脂の中の一種であ
って、圧縮成形可能であっても通常の射出成形は不可能
な樹脂である。First, the tetrafluoroethylene resin (hereinafter P
(abbreviated as TFE) is a homopolymer of tetrafluoroethylene, manufactured by Montegisson in Italy: Hyflon, manufactured by DuPont in the United States: Teflon, and manufactured by ICI&! in the United Kingdom. =
It is a type of fluororesin that is commercially available under the respective registered trademark names such as Fluon and Polyflon (manufactured by Daikin Industries, Ltd.), and although it is compression moldable, ordinary injection molding is not possible.
つぎに、この発明における炭素繊維は、平均繊維径がl
〜20/III、好ましくは5〜15μ麿で、しかもア
スペクト比が1〜50、好ましくは5〜30のものであ
る。なぜならば、平均繊維径が1μ未満の細いものでは
繊維間の凝集が起こり、均一分散が困難となり、また2
0−を越える太いものでは軟質相手材を摩耗させ、アス
ペクト比が1未満のものではマトリックス自体の補強効
果が損われ機械的特性が低下し、逆に50を越えると混
合時の均−分散がきわめて困難であって、摩耗特性に支
障を来たし品質低下を招くなど好ましくないからである
。Next, the carbon fiber in this invention has an average fiber diameter of 1
~20/III, preferably 5 to 15 μm, and an aspect ratio of 1 to 50, preferably 5 to 30. This is because if the average fiber diameter is less than 1μ, the fibers will aggregate, making uniform dispersion difficult, and
If the aspect ratio exceeds 0, it will wear out the soft mating material, if the aspect ratio is less than 1, the reinforcing effect of the matrix itself will be impaired and the mechanical properties will deteriorate, and if it exceeds 50, the uniform dispersion during mixing will deteriorate. This is because it is extremely difficult and undesirable as it impedes the wear characteristics and leads to quality deterioration.
そして、このような望ましい炭素繊維には、東し社製:
トレカーLD−30、呉羽化学工業社製:クレカM2O
1S、同M2O07Sなどを例示することができる。And, such desirable carbon fibers are manufactured by Toshisha:
Trading car LD-30, manufactured by Kureha Chemical Industry Co., Ltd.: Credit card M2O
Examples include 1S and M2O07S.
さらに、この発明におけるカルシウム化合物は、カルシ
ウムの炭酸塩、硫酸塩、酸化物、水酸化物であって、中
でも炭酸カルシウムおよび硫酸カルシウムが好ましい、
これらカルシウム化合物の平均粒径を0.5〜40μ好
ましくは1〜30μmの範囲に限定する理由は、0.5
itm未満の小粒では粒子間の凝集が起こり、均一分散
が困難となり、また40u+を越える大粒では表面平滑
性が悪くなって好ましくないからである。Furthermore, the calcium compound in this invention is a carbonate, sulfate, oxide, or hydroxide of calcium, and calcium carbonate and calcium sulfate are particularly preferred.
The reason why the average particle size of these calcium compounds is limited to a range of 0.5 to 40 μm, preferably 1 to 30 μm is that 0.5
This is because if the particle size is less than itm, agglomeration between particles will occur, making uniform dispersion difficult, and if the particle size is larger than 40u+, the surface smoothness will deteriorate, which is undesirable.
これらのこの発明における必須成分の配合割合をそれぞ
れ炭素繊112〜2帽1%、好ましくは5〜20重匿%
、カルシウム化合物0.5〜50重量%、好ましくは2
〜35重量%、残部を四フッ化エチレン樹脂とする理由
は、炭素繊維が前記下限値未満の少量では耐摩耗性の向
上を殆ど期待することが出来ず、また上限値を越える多
量のときは軟質相手材を摩耗させるようになり、カルシ
ウム化合物が上記の下限値未満の少量のときも同様に軟
質相手材を摩耗させ、逆に上限値を越える多量のときに
は機械的特性の低下を招き好ましくないからである。The blending ratio of these essential components in this invention is 112% to 1% carbon fiber, preferably 5% to 20% carbon fiber.
, calcium compound 0.5-50% by weight, preferably 2
~35% by weight, with the remainder being tetrafluoroethylene resin.The reason is that if the amount of carbon fiber is less than the lower limit, little improvement in wear resistance can be expected, and if the amount exceeds the upper limit, Calcium compounds start to wear out the soft mating material, and when the calcium compound is in a small amount below the lower limit above, it also wears out the soft mating material, and on the other hand, when the calcium compound is in a large amount exceeding the upper limit, it causes a decrease in mechanical properties, which is undesirable. It is from.
以上の割合で配合される混合物は、従来から広く行なわ
れている充填材入りPTFEIに対する通常の成形条件
で成形すればよ(、たとえばタンブラ−ミキサー ヘン
シェルミキサー等の混合機によってPTF[!、炭素繊
維、カルシウム化合物の三成分を乾式混合し、これを金
型に入れて380〜600kg/iの圧力を加えて予備
成形した後、金型から取り出された圧縮成形体を370
℃で焼結する方法、その油加熱加圧しながら回分式圧縮
成形する方法またはラム押出し機によって連続式押出し
成形を行なう方法などいずれであってもよい、なお、こ
の発明の樹脂組成物においても、通常の樹脂組成物の場
合と同様に、この発明の主目的を阻害しない範囲内で、
たとえば、炭素粉、ケイ石粉、二硫化モリブデンなどの
固体潤滑剤、ガラス繊維、ホウ素繊維、炭化ケイ素繊維
、石綿、岩綿、金属繊維などの強化剤、二酸化アンチモ
ン、炭酸マグネシウムなどの難燃剤、クレー、マイカ、
石綿、シリカ、グラファイト等の電気特性改良剤、硫酸
バリウム、シリカなどの耐酸性向上剤、ガラスピーズ、
ガラス球、アルミナ、タルク、ケイ藻土、水和アルミナ
、シラスバルーン、その他金属酸化物等の増量剤、さら
には顔料など、いずれも380℃程度以上の高1で安定
な物質を適宜混合してもよい。The mixture blended in the above proportions can be molded under the usual molding conditions for PTFEI with fillers that have been widely used in the past (for example, PTF [!, carbon fiber , the three components of the calcium compound are dry mixed, put into a mold and preformed by applying a pressure of 380 to 600 kg/i, and then the compression molded body taken out from the mold is
℃ sintering, batch compression molding while heating and pressurizing oil, or continuous extrusion using a ram extruder. In addition, in the resin composition of the present invention, As in the case of ordinary resin compositions, within a range that does not impede the main purpose of this invention,
For example, solid lubricants such as carbon powder, silica powder, and molybdenum disulfide; reinforcing agents such as glass fiber, boron fiber, silicon carbide fiber, asbestos, rock wool, and metal fiber; flame retardants such as antimony dioxide and magnesium carbonate; , mica,
Electrical property improvers such as asbestos, silica, and graphite, acid resistance improvers such as barium sulfate and silica, glass beads,
Glass bulbs, alumina, talc, diatomaceous earth, hydrated alumina, shirasu balloons, fillers such as other metal oxides, and even pigments, all of which are stable at high temperatures of about 380°C or higher, are appropriately mixed. Good too.
このような添加剤を添加する際の残部口フフ化エチレン
樹脂の配合割合は、151℃量%を下回らないようにす
るのがよい。When such additives are added, the blending ratio of the remaining fluorinated ethylene resin is preferably not less than 151° C. mass %.
以下に述べる実施例および比較例に使用した原材料を一
括して示すとつぎのとおりである。なお〔〕内にはそれ
ぞれの略号を記入し、また配合割合は重量%である。The raw materials used in the Examples and Comparative Examples described below are listed below. In addition, the respective abbreviations are written in brackets [ ], and the blending ratio is in weight %.
■四フシ化エチレン樹脂(PTFII)(ヌルデュポン
フロロケミカル社製:テフロン7J。■Tetrafluoroethylene resin (PTFII) (manufactured by Null DuPont Fluorochemical Co., Ltd.: Teflon 7J.
粉末)、
■炭素繊維(CF−1)
(東し社製:トレカMLD30、平均ta維径7μm、
アスペクト比1〜30)、
■炭素繊維[CF−2]
(呉羽化学工業社製;クレ力−2013、平均1m径1
2.5JI鵬、アスペクト比1〜40)、■炭酸カルシ
ウム(CaC05)
(日量工業社製= N^600、平均粒径7μm)、■
硫酸カルシウム(Ca5Os)
(和光純薬工業社製:試薬級、平均粒径Iμ−)、実施
例1〜5:
各原材料を第1表に示す割合で乾式配合し、これを金型
に入れて550kg/c−の加圧下で予備成形した後、
金型から取り出された圧縮成形体を370℃で焼結成形
体とし、この成形体から各種試験方法に規定されている
寸法、形状の試験片を作製した。なお、各種試験方法は
つぎのとおりである。powder), ■Carbon fiber (CF-1) (manufactured by Toshisha: Torayka MLD30, average ta fiber diameter 7 μm,
Aspect ratio 1 to 30), ■Carbon fiber [CF-2] (manufactured by Kureha Chemical Industry Co., Ltd.; Kureki-2013, average 1m diameter 1
2.5 JI Peng, aspect ratio 1-40), ■ Calcium carbonate (CaC05) (manufactured by Nichiryo Kogyo Co., Ltd. = N^600, average particle size 7 μm), ■
Calcium sulfate (CaOs) (manufactured by Wako Pure Chemical Industries, Ltd.: reagent grade, average particle size Iμ-), Examples 1 to 5: Each raw material was dry blended in the proportions shown in Table 1, and this was put into a mold. After preforming under a pressure of 550 kg/c-,
The compression molded body taken out from the mold was sintered at 370° C., and test pieces having dimensions and shapes specified in various test methods were produced from this molded body. The various test methods are as follows.
(])引張り強度(kg/ej)および伸び(%)AS
Tl’l−0638に準拠、
(2)線膨張係数(XIO−’/’C)^5T)1−D
695に準拠、
(3)摩擦試験
スラスト型摩擦試験機による滑り速度毎分150m、1
重1.1kg/cj、相手材へ〇(ニー12 (T6処
理)、潤滑油スニソ4GSの強制潤滑条件下の摩擦係数
を求める。(]) Tensile strength (kg/ej) and elongation (%) AS
Based on Tl'l-0638, (2) Linear expansion coefficient (XIO-'/'C)^5T)1-D
695, (3) Friction test Sliding speed by thrust type friction tester 150 m/min, 1
Find the friction coefficient under forced lubrication conditions, weight 1.1 kg/cj, mating material 〇 (knee 12 (T6 treatment), lubricant Suniso 4GS).
(4)摩耗係数(xlO−” cj/kg −m)低P
V条件として、スラスト型摩耗試験機による滑り速度毎
分96m、荷重5 kg / cd、相手材^0C12
(’r6処理)、潤滑油スニソ4GSの強制潤滑条件を
選びその摩耗係数を求める。また、高PV条件として、
スラスト型摩耗試験機による滑り速度毎分128m、荷
重tokg/e+J、その他は前記低PV条件の場合と
同一の条件を選び、そのときの摩耗係数を求める。(4) Wear coefficient (xlO-”cj/kg-m) Low P
The V conditions were a sliding speed of 96 m/min using a thrust type abrasion tester, a load of 5 kg/cd, and a mating material ^0C12.
('r6 processing), select the forced lubrication conditions of lubricating oil Suniso 4GS and find its wear coefficient. In addition, as a high PV condition,
A sliding speed of 128 m/min using a thrust type abrasion tester, a load of tokg/e+J, and the other conditions are the same as those for the low PV condition described above, and the wear coefficient at that time is determined.
以上の各試験によって得られた結果を第1表に併記した
。The results obtained from each of the above tests are also listed in Table 1.
比較例1〜4;
各原材料の配合割合が第2表に示すとおりである以外は
実施例1〜5と全く同様にして試験片を作製し、各種試
験を行なった。得られた結果を第2表に併記した。Comparative Examples 1 to 4; Test pieces were prepared in exactly the same manner as Examples 1 to 5, except that the proportions of each raw material were as shown in Table 2, and various tests were conducted. The obtained results are also listed in Table 2.
第1表
第2′a
第1表および第2表からつぎのことが明らかである。す
なわち、この発明の摺動品材料用組成物からなる実施例
1〜5で得られた成形体は、いずれも均衡のとれた機械
的特性を現わし、軟質相手材に対する高PV条件下にお
ける心動特性もきわめて優れていて、両面のバランスは
非常に良好である。これに対して、炭素繊維の添加量が
この発明の限定範囲外である場合の比較例2は、特に高
PV条件下における摩耗係数が大きく、また比較例4は
相手材の摩耗が大きく、摩擦係数も高く、さらには、機
械的特性の一つである引張り伸びにおいて著しい低下を
招くものであった。また、カルシウム化合物の添加量が
この発明の限定範囲外である比較例1における成形体は
相手材の摩耗が大きく、比較例3における成形体も特に
高PV条件における摩耗が太き(、摩擦係数も高く、さ
らに機械的特性の一つである引張り伸びも著しい低下を
招くものであった。これら比較例1〜4は実施例1〜5
のいずれよりもかなり劣ったものであり、好ましいもの
ではなかった。Table 1, Section 2'a The following is clear from Tables 1 and 2. In other words, the molded bodies obtained in Examples 1 to 5 comprising the composition for sliding article materials of the present invention all exhibited balanced mechanical properties, and exhibited a high resistance to heart motion under high PV conditions relative to the soft mating material. The properties are also very good, and the balance on both sides is very good. On the other hand, in Comparative Example 2, in which the amount of carbon fiber added was outside the limited range of the present invention, the wear coefficient was large especially under high PV conditions, and in Comparative Example 4, the wear of the mating material was large and the friction The coefficient was also high, and furthermore, the tensile elongation, which is one of the mechanical properties, was significantly reduced. In addition, the molded body in Comparative Example 1, in which the amount of calcium compound added was outside the limited range of the present invention, had a large amount of wear on the mating material, and the molded body in Comparative Example 3 also had large wear, especially under high PV conditions (friction coefficient Furthermore, the tensile elongation, which is one of the mechanical properties, was also significantly decreased.
It was considerably inferior to any of the above, and was not desirable.
炭素繊維およびカルシウム化合物を四フッ化エチレン樹
脂に配合して得られたこの発明の摺動品材料用組成物は
、従来のガラス繊維、炭素繊維、各種金属粉末などを配
合したものよりも自己および相手材の摩耗を著しく低減
させることができ、特に軟質相手材に対して高PV条件
下での摺動特性が優れ、たとえばコンプレッサー用シー
ルリング等アルミニウム材相手の高PV条件下における
摺動部部品製造には非常に有利な材料となり得るのであ
る。The composition for sliding article materials of the present invention, which is obtained by blending carbon fibers and calcium compounds with tetrafluoroethylene resin, has a higher self- and Abrasion of the mating material can be significantly reduced, and the sliding properties are particularly excellent against soft mating materials under high PV conditions.For example, sliding parts such as seal rings for compressors under high PV conditions of aluminum mating materials. It can be a very advantageous material for manufacturing.
特許出願人 洋ベア・ルーロン工業株式会社同 代理
人
鎌
田
文Patent applicant: Western Bear Rulon Industrial Co., Ltd. Agent: Aya Kamata
Claims (1)
1〜50である炭素繊維2〜30重量%と、平均粒径が
0.5〜40μmであるカルシウム化合物粉末0.5〜
50重量%とを必須成分として含有し、残部が四フッ化
エチレン樹脂である摺動部材料用組成物。(1) 2 to 30% by weight of carbon fibers with an average fiber diameter of 1 to 20 μm and an aspect ratio of 1 to 50, and 0.5 to 30% of calcium compound powder with an average particle diameter of 0.5 to 40 μm.
50% by weight as an essential component, and the remainder being tetrafluoroethylene resin.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1042768A JP2824075B2 (en) | 1989-02-22 | 1989-02-22 | Molded body of composition for sliding part material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1042768A JP2824075B2 (en) | 1989-02-22 | 1989-02-22 | Molded body of composition for sliding part material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02219895A true JPH02219895A (en) | 1990-09-03 |
JP2824075B2 JP2824075B2 (en) | 1998-11-11 |
Family
ID=12645154
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1042768A Expired - Lifetime JP2824075B2 (en) | 1989-02-22 | 1989-02-22 | Molded body of composition for sliding part material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2824075B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002327750A (en) * | 2001-04-27 | 2002-11-15 | Ntn Corp | Multi-layered bearing |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5273275A (en) * | 1975-12-12 | 1977-06-18 | Phillips Petroleum Co | Selfflubricating composion or molded product of the like |
JPS62184225A (en) * | 1986-01-21 | 1987-08-12 | コルベンシユミツト・アクチエンゲゼルシヤフト | Composite material for sliding bearing and manufacture thereof |
-
1989
- 1989-02-22 JP JP1042768A patent/JP2824075B2/en not_active Expired - Lifetime
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5273275A (en) * | 1975-12-12 | 1977-06-18 | Phillips Petroleum Co | Selfflubricating composion or molded product of the like |
JPS62184225A (en) * | 1986-01-21 | 1987-08-12 | コルベンシユミツト・アクチエンゲゼルシヤフト | Composite material for sliding bearing and manufacture thereof |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002327750A (en) * | 2001-04-27 | 2002-11-15 | Ntn Corp | Multi-layered bearing |
Also Published As
Publication number | Publication date |
---|---|
JP2824075B2 (en) | 1998-11-11 |
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