JP2525490B2 - Plastic cage for bearing - Google Patents
Plastic cage for bearingInfo
- Publication number
- JP2525490B2 JP2525490B2 JP1326089A JP32608989A JP2525490B2 JP 2525490 B2 JP2525490 B2 JP 2525490B2 JP 1326089 A JP1326089 A JP 1326089A JP 32608989 A JP32608989 A JP 32608989A JP 2525490 B2 JP2525490 B2 JP 2525490B2
- Authority
- JP
- Japan
- Prior art keywords
- cage
- polyimide resin
- weight
- resin
- bearing
- 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 - Lifetime
Links
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16C—SHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
- F16C33/00—Parts of bearings; Special methods for making bearings or parts thereof
- F16C33/30—Parts of ball or roller bearings
- F16C33/38—Ball cages
- F16C33/41—Ball cages comb-shaped
- F16C33/412—Massive or moulded comb cages, e.g. snap ball cages
- F16C33/414—Massive or moulded comb cages, e.g. snap ball cages formed as one-piece cages, i.e. monoblock comb cages
- F16C33/416—Massive or moulded comb cages, e.g. snap ball cages formed as one-piece cages, i.e. monoblock comb cages made from plastic, e.g. injection moulded comb cages
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16C—SHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
- F16C33/00—Parts of bearings; Special methods for making bearings or parts thereof
- F16C33/30—Parts of ball or roller bearings
- F16C33/38—Ball cages
- F16C33/44—Selection of substances
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16C—SHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
- F16C19/00—Bearings with rolling contact, for exclusively rotary movement
- F16C19/02—Bearings with rolling contact, for exclusively rotary movement with bearing balls essentially of the same size in one or more circular rows
- F16C19/04—Bearings with rolling contact, for exclusively rotary movement with bearing balls essentially of the same size in one or more circular rows for radial load mainly
- F16C19/06—Bearings with rolling contact, for exclusively rotary movement with bearing balls essentially of the same size in one or more circular rows for radial load mainly with a single row or balls
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16C—SHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
- F16C2208/00—Plastics; Synthetic resins, e.g. rubbers
- F16C2208/20—Thermoplastic resins
- F16C2208/40—Imides, e.g. polyimide [PI], polyetherimide [PEI]
Landscapes
- Engineering & Computer Science (AREA)
- General Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Rolling Contact Bearings (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 この発明は、過酷な条件下で使用される各種軸受用保
持器に関する。更に詳細には、耐熱性、耐油性、耐薬品
性、成形性等に優れる熱可塑性樹脂組成物からなる各種
軸受用保持器に関する。TECHNICAL FIELD The present invention relates to a cage for various bearings used under severe conditions. More specifically, the present invention relates to various bearing cages made of a thermoplastic resin composition having excellent heat resistance, oil resistance, chemical resistance, moldability, and the like.
一般に、転がり軸受は、転動体の種類により玉軸受と
ころ軸受とに分類される。転がり軸受の保持器について
更に細かく分類して代表的なものを挙げるとすると、玉
軸受については、例えば、一般タイプ保持器、冠型保持
器およびアンギュラ軸受用スラスト玉軸受等の保持器が
ある。一方、ころ軸受については、例えば、円錐ころ軸
受用保持器、球面ころ軸受用保持器、円筒ころ軸受用保
持器、スラストころ軸受用保持器、スラスト球面軸受用
保持器等のころ軸受用保持器がある。Generally, rolling bearings are classified into ball bearings and bearings depending on the type of rolling elements. To further classify cages of rolling bearings in more detail and to cite typical ones, examples of ball bearings include cages such as general type cages, crown type cages, and thrust ball bearings for angular bearings. On the other hand, as for the roller bearing, for example, a roller bearing retainer such as a tapered roller bearing retainer, a spherical roller bearing retainer, a cylindrical roller bearing retainer, a thrust roller bearing retainer, and a thrust spherical bearing retainer. There is.
プラスチック製の転がり軸受用保持器(以下、保持器
と略称する)としては、成形性、柔軟性などの機械的諸
特性および原材料費等の生産性に優れたポリアミド系樹
脂を素材とする、いわゆるナイロン製保持器が、従来よ
り広く用いられている。保持器の一例として、冠型保持
器の要部を第1図に示す。この保持器1は、その上部に
爪部2を有しており、出入口が狭小になっているポケッ
ト部3に鋼球等の転動体4を組込んで回転自在に保持す
るものである。As a cage for rolling bearings made of plastic (hereinafter, abbreviated as a cage), a so-called polyamide resin having excellent mechanical properties such as moldability and flexibility and productivity such as raw material cost is used. Nylon cages have been widely used. As an example of the cage, a main part of a crown type cage is shown in FIG. This cage 1 has a claw portion 2 on its upper portion, and a rolling element 4 such as a steel ball is incorporated in a pocket portion 3 having a narrow entrance and exit to rotatably retain the rolling element 4.
しかしナイロン製の保持器は、100℃以上の連続使用
温度条件下において、または極圧添加剤等が添加されて
油類やその他の酸性の薬剤と接触する条件下においては
ナイロンが劣化し、その所望の特性が失なわれるので、
そのような条件下で使用するにはあまり適していない。However, the cage made of nylon deteriorates under the conditions of continuous use temperature of 100 ° C. or higher, or under the condition that extreme pressure additives are added and it comes into contact with oils and other acidic chemicals. Since the desired properties are lost,
Not very suitable for use under such conditions.
このようなナイロンに代わる素材であって、高温度条
件下で使用可能であり、比較的廉価な材料に、ポリフェ
ニレンサルファイド樹脂(以下、PPS樹脂と記す)があ
り、これは耐熱性とともに耐薬品性、成形性などにも優
れている。このPPS樹脂は、下記一般式 で表わされる繰返し単位からなる重合体である。このよ
うな重合体は、例えば、硫化ナトリウムとP−ジクロル
ベンゼンとをN−メチルピロリドン、ジメチルアセトア
ミド等のアミド系溶媒若しくはスルホラン等のスルホン
系溶媒中で反応させて得られ、この段階のPPS樹脂を重
合上りとしている。また、PPS樹脂には架橋性PPS樹脂
(分岐状PPS樹脂とも呼ばれる)と直鎖状PPS樹脂の2種
類がある。前者の架橋性PPS樹脂は、例えば重合上りの
溶融粘度が約20〜100ポアズぐらいの低粘度低分子量のP
PS樹脂を空気中において融点以下に加熱して、酸化架橋
させ、溶融粘度を高めたり、あるいは意図的に架橋剤や
分岐剤を添加することにより架橋または分岐構造を導入
し、溶融粘度を高めたりしている。Polyphenylene sulfide resin (hereinafter referred to as PPS resin) is a material that can be used under high temperature conditions and is a relatively inexpensive material that can replace nylon, and it has heat resistance and chemical resistance. It also has excellent moldability. This PPS resin has the following general formula It is a polymer comprising a repeating unit represented by: Such a polymer is obtained, for example, by reacting sodium sulfide and P-dichlorobenzene in an amide solvent such as N-methylpyrrolidone or dimethylacetamide or a sulfone solvent such as sulfolane. The resin is polymerized. There are two types of PPS resins, a crosslinkable PPS resin (also called a branched PPS resin) and a linear PPS resin. The former crosslinkable PPS resin has a low viscosity and a low molecular weight P, for example, a melt viscosity after polymerization of about 20 to 100 poise.
The PS resin is heated to a temperature below its melting point in air to oxidize and crosslink to increase the melt viscosity, or by intentionally adding a crosslinking agent or branching agent to introduce a crosslink or branch structure to increase the melt viscosity. are doing.
しかし、このようにして得られた架橋性PPS樹脂は、
溶融粘度が高められ、すなわち、耐熱性は向上している
が、かなり脆くなっており柔軟性に欠ける。したがっ
て、転動体4をポケット部3へ組込む際に柔軟性が必要
とされる保持器の素材としては不適当である。However, the crosslinkable PPS resin thus obtained is
The melt viscosity is increased, that is, the heat resistance is improved, but it is considerably brittle and lacks flexibility. Therefore, it is unsuitable as a material for a cage that requires flexibility when the rolling element 4 is assembled in the pocket 3.
一方、直鎖状PPS樹脂は重合段階で直鎖状に分子鎖を
高分子量にまで成長させたPPS樹脂であり、前記の架橋
性PPS樹脂に比べると、非常に柔軟で靭性が大きいとい
う特徴がある。この点に着目して、直鎖状PPS樹脂を軸
受用保持器として使用する提案が特開昭64−79419号公
報に開示されている。しかし、この直鎖状PPS樹脂から
成る軸受用保持器は、組み立て時の組み込み性には優れ
ているが、熱安定性や高温(150℃以上)での耐クリー
プ特性等の機械的特性等が劣っている。したがって、保
持器が遠心力によって変形し、外輪と接触して異常な摩
擦熱が発生する結果、潤滑剤を劣化させ、軸受の性能を
低下させる場合がある。On the other hand, the linear PPS resin is a PPS resin in which the molecular chain is linearly grown to a high molecular weight in the polymerization stage, and is characterized by being extremely flexible and tough as compared with the above-mentioned crosslinkable PPS resin. is there. Focusing on this point, a proposal of using a linear PPS resin as a bearing retainer is disclosed in Japanese Patent Laid-Open No. 64-79419. However, the bearing cage made of this linear PPS resin is excellent in assembling at the time of assembly, but it has thermal stability and mechanical characteristics such as creep resistance at high temperature (150 ° C or higher). Inferior Therefore, the cage may be deformed by the centrifugal force and contact with the outer ring to generate abnormal frictional heat. As a result, the lubricant may be deteriorated and the performance of the bearing may be deteriorated.
150℃以上を超えるような高温状態において比較的安
定な素材としては、ポリエーテルスルホン(以下、PES
と記す)、ポリエーテルイミド(以下、PEIと記す)、
ポリアミドイミド(以下、PAIと記す)、ポリエーテル
エーテルケトン(以下、PEEKと記す)等のスーパーエン
ジニアリングプラスチックが挙げられる。しかし、これ
らの何れも、軸受用保持器に使用するには以下のように
不十分である。Polyethersulfone (hereinafter referred to as PES) is a relatively stable material at high temperatures above 150 ° C.
, Polyetherimide (hereinafter referred to as PEI),
Examples include super engineering plastics such as polyamide-imide (hereinafter referred to as PAI) and polyether ether ketone (hereinafter referred to as PEEK). However, none of these is sufficient for use in a bearing cage as described below.
PESは高いガラス転移点(約225℃)を有しているが、
例えば、ケトン、エステル、エーテル類などの極性化合
物に対して耐性が無く、グリースに含有される極圧添加
剤により浸される危険性が有る。PES has a high glass transition temperature (about 225 ° C),
For example, there is no resistance to polar compounds such as ketones, esters, ethers, etc., and there is a risk of being immersed by the extreme pressure additive contained in the grease.
PEIおよびPEEKは柔軟性に欠けるので、転動体の組み
込み性の問題がある。また、転動体からの衝撃により爪
等の欠けが発生する場合も有る。Since PEI and PEEK are inflexible, there is a problem of rolling element assembling. In addition, the impact from the rolling element may cause chipping of the nail or the like.
PAIは、この樹脂特有の高吸水性に起因して急加熱に
よる膨れや発泡が発生する傾向にある。更にグリース等
に含まれる極圧添加剤中のアルカリ分によって加水分解
する危険性がある。PAI tends to swell and foam due to rapid heating due to the high water absorption characteristic of this resin. Further, there is a risk of hydrolysis due to the alkali component in the extreme pressure additive contained in grease or the like.
更に、射出成形可能で耐熱性300℃を有する樹脂とし
て液晶ポリマー(以下、LCPと記す)がある。しかし、
このLCPには特有の樹脂配向性により配向方向に対し垂
直方向の力には強いが、配向方向に対して平行な力には
非常に弱い。複雑異形状である保持器においては、配向
方向に平行な力が加わる危険性が十分あるので、LCPを
保持器に使用するのは不適当である。Further, there is a liquid crystal polymer (hereinafter referred to as LCP) as a resin that can be injection-molded and has a heat resistance of 300 ° C. But,
This LCP is strong in the force in the direction perpendicular to the alignment direction due to the peculiar resin orientation, but is very weak in the force parallel to the alignment direction. In the case of a cage having a complicated shape, there is a sufficient risk of applying a force parallel to the orientation direction, and therefore it is not appropriate to use the LCP for the cage.
また、ポリイミド系材料として350℃以上の耐熱性を
有するベスペルSP 21(デュポン社製)があるが、これ
は射出成形不能なので、成形の場合には、圧縮成形後切
削加工が必要となる。Also, as a polyimide material, there is Vespel SP 21 (manufactured by DuPont) having heat resistance of 350 ° C. or higher, but this cannot be injection-molded, so in the case of molding, cutting after compression molding is required.
この発明は、そのような課題を解決すべくなされたも
のである。すなわちこの発明の目的は、耐熱性、耐油
性、耐薬品性、射出成形性、耐熱変形性などの各種特性
を全て具備する軸受用プラスチック保持器を提供するこ
とにある。The present invention has been made to solve such a problem. That is, an object of the present invention is to provide a plastic cage for bearings having all of various characteristics such as heat resistance, oil resistance, chemical resistance, injection moldability, and heat distortion resistance.
この発明は、ポリイミド樹脂、潤滑剤及び繊維状補強
剤よりなるポリイミド系樹脂組成物からなり、当該ポリ
イミド樹脂が下記一般式 で示される繰り返し単位からなる熱可塑性ポリイミド樹
脂であって、該熱可塑性ポリイミド樹脂粉末0.5gを100m
lのp−クロロフェノール/フェノール混合溶媒(混合
重量比90:10)に加熱溶解した溶液の35℃における溶液
粘度が0.35〜0.80dl/gであり、かつ、該ポリイミド系樹
脂組成物の総量中に、(i)5〜50重量%のフッ素樹
脂、黒鉛及び二硫化モリブデンより選ばれた少なくとも
1種の潤滑剤及び(ii)0〜50重量%のガラス繊維、カ
ーボン繊維、ボロン繊維、炭化ケイ素繊維、カーボンウ
イスカー、アスベスト、金属繊維及びロックウールより
選ばれた少なくとも1種の繊維状補強剤からなる添加剤
を含み、かつ該添加剤(i)(ii)の合計量が5〜60重
量%であることを特徴とする軸受用プラスチック保持器
である。This invention comprises a polyimide resin composition comprising a polyimide resin, a lubricant and a fibrous reinforcing agent, wherein the polyimide resin has the following general formula: A thermoplastic polyimide resin consisting of repeating units represented by 100 g of the thermoplastic polyimide resin powder 0.5 g
of p-chlorophenol / phenol mixed solvent (mixing weight ratio: 90:10) having a solution viscosity at 35 ° C. of 0.35 to 0.80 dl / g, and in the total amount of the polyimide resin composition. And (i) 5 to 50% by weight of a fluororesin, at least one lubricant selected from graphite and molybdenum disulfide, and (ii) 0 to 50% by weight of glass fiber, carbon fiber, boron fiber, silicon carbide. An additive comprising at least one fibrous reinforcing agent selected from fibers, carbon whiskers, asbestos, metal fibers and rock wool, and the total amount of the additives (i) and (ii) is 5 to 60% by weight. Is a plastic retainer for bearings.
本発明における熱可塑性ポリイミド樹脂については、
その製造方法に特に限定は無い。しかし通常は、下記式 で表される4,4′−ビス(3−アミノフェノキシ)ビフ
ェニルと、ピロメリット酸二無水物とを反応させること
によってポリアミド酸を生成させ、そのポリアミド酸を
脱水環化して得ることができる。Regarding the thermoplastic polyimide resin in the present invention,
The manufacturing method is not particularly limited. However, normally, It can be obtained by reacting 4,4'-bis (3-aminophenoxy) biphenyl represented by and pyromellitic dianhydride to generate a polyamic acid, and dehydrating and cyclizing the polyamic acid.
熱可塑性ポリイミド樹脂の溶液粘度は、0.35〜0.80dl
/gである。その最適な値は、保持器の用途によって求め
られる物性の程度が若干異なるので、一概にはいえない
が、0.45〜0.55dl/g程度が好ましい。The solution viscosity of thermoplastic polyimide resin is 0.35-0.80dl
/ g. The optimum value cannot be unequivocally determined because the degree of physical properties required depends on the use of the cage, but it is preferably 0.45 to 0.55 dl / g.
なお、以上の熱可塑性ポリイミド樹脂の他に、この発
明の目的を損なわない範囲で、通常の樹脂組成物に広く
用いられている添加剤類を配合しても良い。その添加率
はそれぞれ比重が異なるため重量部では表現し難いが体
積部ではポリイミド樹脂100部に対して5〜50体積部が
望ましく、15〜35体積部が好ましい。特に、本発明にお
いて、添加剤として、5〜50重量%(好ましくは10〜40
重量%)の潤滑剤(下記に挙げる潤滑剤より選ばれた少
なくとも1種)及び0〜50重量%(好ましくは0〜40重
量%)の繊維状補給剤(下記に挙げる繊維状補強剤より
選ばれた少なくとも1種)を含み、そして添加剤合計量
で5〜60重量%(好ましくは10〜50重量%)の範囲内で
配合する。使用可能な添加剤類を以下に列挙する。In addition to the above thermoplastic polyimide resins, additives widely used in ordinary resin compositions may be blended within a range that does not impair the object of the present invention. It is difficult to express the addition rate in parts by weight because the specific gravities are different from each other, but in volume part, 5 to 50 parts by volume, and preferably 15 to 35 parts by volume, relative to 100 parts of the polyimide resin are preferable. Particularly, in the present invention, as an additive, 5 to 50% by weight (preferably 10 to 40% by weight) is used.
Wt%) lubricant (at least one selected from the lubricants listed below) and 0 to 50 wt% (preferably 0 to 40 wt%) fibrous replenisher (selected from the fibrous reinforcing agents listed below). The total amount of additives is 5 to 60% by weight (preferably 10 to 50% by weight). The additives that can be used are listed below.
潤滑剤: フッ素樹脂、黒鉛、二硫化モリブデン 繊維状補強剤: ガラス繊維、カーボン繊維、ボロン繊維、炭化ケイ素
繊維、カーボンウイスカー、アスベスト、金属繊維、ロ
ックウール 難燃性向上剤: 三酸化アンチモン、炭酸マグネシウム、炭酸カルシウ
ム等 電気特性向上剤: クレー、マイカ等 耐トラッキング向上剤: 石綿、シリカ、グラファイト等 熱伝導度向上剤: 鉄、亜鉛、アルミニウム、銅等の金属粉末等 その他: ガラスビーズ、ガラス球、炭酸カルシウム、アルミ
ナ、タルク、ケイソウ土、水和アルミナ、シラスバルー
ン、各種金属酸化物、無機質含量類等で500℃以上で安
定な天然若しくは合成の化合物類 以上の熱可塑性ポリイミド樹脂組成物を用いて、通常
の射出成形方法によって、この発明の保持器を容易に成
形することができる。したがって、圧縮成形後に切削加
工する等の煩雑な成形法は必要とならない。また、本発
明の保持器は、その種類については特に限定はなく、先
に例示したような、一般タイプ保持器、冠型保持器等各
種の保持器とすることができる。Lubricant: Fluororesin, graphite, molybdenum disulfide Fibrous reinforcing agent: Glass fiber, carbon fiber, boron fiber, silicon carbide fiber, carbon whiskers, asbestos, metal fiber, rock wool Flame retardant: Antimony trioxide, carbonic acid Magnesium, calcium carbonate, etc. Electric property improver: Clay, mica, etc. Tracking resistance improver: Asbestos, silica, graphite etc. Thermal conductivity improver: Metal powder such as iron, zinc, aluminum, copper etc. Others: Glass beads, glass balls , Calcium carbonate, alumina, talc, diatomaceous earth, hydrated alumina, shirasu balloon, various metal oxides, natural or synthetic compounds that are stable at 500 ° C or higher with various inorganic contents. Use the above thermoplastic polyimide resin composition. The cage of the present invention can be easily molded by a normal injection molding method. Can. Therefore, a complicated molding method such as cutting after compression molding is not required. Further, the type of the cage of the present invention is not particularly limited, and various types of cages such as the general type cage and the crown type cage as exemplified above can be used.
以下、この発明を実施例により更に詳細に説明する。 Hereinafter, the present invention will be described in more detail with reference to Examples.
合成例1(ポリイミド樹脂の製造) 撹拌機、還流冷却および窒素導入管を備えた反応容器
に、4,4′−ビス(3−アミノフェノキシ)ビフェニル
3.68kg(10モル)と、N,N−ジメチルアセトアミド32.9k
gを挿入し、室温で窒素雰囲気下にピロメリット酸二無
水物2.125kg(9.75モル)を溶液温度の上昇に注意しな
がら加え、室温で約20時間かきまぜ、ポリアミド酸溶液
を得た。Synthesis Example 1 (Production of Polyimide Resin) 4,4′-bis (3-aminophenoxy) biphenyl was placed in a reaction vessel equipped with a stirrer, reflux cooling and a nitrogen introducing tube.
3.68 kg (10 mol) and N, N-dimethylacetamide 32.9 k
g was added, and 2.125 kg (9.75 mol) of pyromellitic dianhydride was added at room temperature under a nitrogen atmosphere while paying attention to the rise in solution temperature, and the mixture was stirred at room temperature for about 20 hours to obtain a polyamic acid solution.
このポリアミド酸溶液中に、室温で窒素雰囲気下に2.
02kg(20モル)のトリエチルアミンおよび2.55kg(25モ
ル)の無水酢酸を滴下した。これを室温で約20時間撹拌
し、淡黄色スラリーを得た。このスラリーを濾別し、メ
タノールで洗浄し、その後濾別し、180℃で8時間減圧
乾燥して5.28kg(収率約97%)のポリイミド粉を得た。
このポリイミド粉の溶液粘度は0.50dl/gであった。な
お、この溶液粘度は、ポリイミド粉末0.5gを100mlの溶
媒(p−クロロフェノール:フェノール=90:10重量
比)に加熱溶解し、溶解後35℃に冷却して測定した値で
ある。In this polyamic acid solution at room temperature under nitrogen atmosphere 2.
02 kg (20 mol) triethylamine and 2.55 kg (25 mol) acetic anhydride were added dropwise. This was stirred at room temperature for about 20 hours to obtain a pale yellow slurry. The slurry was filtered, washed with methanol, then filtered, and dried under reduced pressure at 180 ° C. for 8 hours to obtain 5.28 kg (yield about 97%) of polyimide powder.
The solution viscosity of this polyimide powder was 0.50 dl / g. The solution viscosity is a value measured by dissolving 0.5 g of polyimide powder in 100 ml of a solvent (p-chlorophenol: phenol = 90: 10 weight ratio) by heating, and cooling to 35 ° C. after the dissolution.
実施例1〜3 表−1に示した配合にて、ヘンシェルミキサーにて乾
式混合した。表−1に示す原材料を以下に列挙する。な
お表−1の配合割合はすべて重量部で示したものであ
る。Examples 1 to 3 The formulations shown in Table 1 were dry mixed with a Henschel mixer. The raw materials shown in Table 1 are listed below. The blending ratios in Table-1 are all shown in parts by weight.
熱可塑性ポリイミド 合成例1で製造したポリイミド樹脂(市販品としては、
三井東圧化学社製:New−TPI) PAI ポリアミドイミド樹脂(アモコ社製、商品名:トーロン
4203) PPS(架橋タイプ) ポリフェニレンサルファイド樹脂(トープレン社製、商
品名:T−4) PPS(リニアタイプ) (呉羽化学工業社製、商品名:KSP−#214) PTFE L169 テトラフルオロエチレン樹脂(旭硝子社製、商品名:ル
ーブリカントL169) 黒鉛 鐘紡社製、商品名:ベルパールC2000 ガラスファイバー (日本電気硝子社製、商品名:ECSO3T747DE) カーボンファイバー (東邦レーヨン社製、商品名:HTA−C6X603) 乾式混合後、二軸溶融押出機を用いて370℃〜400℃で
押出して造粒し、得られたペレットを射出成形機(シリ
ンダー温度370〜400℃、射出圧力1000kg/cm2、金型温度
150〜200℃)に供給し、後述する各試験法に定められた
試験片を成形し、摩擦摩耗特性、曲げ強度、曲げ弾性
率、軟化温度を測定した。得られた結果を表−1に示
す。なお、各試験方法は次のとおりである。Thermoplastic Polyimide Polyimide resin produced in Synthesis Example 1 (commercially available,
Mitsui Toatsu Chemicals: New-TPI PAI Polyamideimide resin (Amoco, trade name: Torlon
4203) PPS (Cross-linking type) Polyphenylene sulfide resin (Torprene Co., trade name: T-4) PPS (Linear type) (Kureha Chemical Industry Co., Ltd., trade name: KSP- # 214) PTFE L169 Tetrafluoroethylene resin (Asahi Glass Company, product name: Lubricant L169) Graphite Kanebo, product name: Bell Pearl C2000 glass fiber (Nippon Electric Glass, product name: ECSO3T747DE) Carbon fiber (Toho Rayon, product name: HTA-C6X603) Dry type After mixing, extrude at 370 ℃ ~ 400 ℃ using a twin-screw extruder and granulate, the obtained pellets are injection molding machine (cylinder temperature 370 ~ 400 ℃, injection pressure 1000 kg / cm 2 , mold temperature
150 to 200 ° C.), the test pieces defined in each test method described later were molded, and the friction and wear characteristics, bending strength, bending elastic modulus, and softening temperature were measured. Table 1 shows the obtained results. In addition, each test method is as follows.
(1)組み立て時の組み込み性試験 第2図に示すようにミニプレスにて実際に軸受本体5
に組み込んで保持器1の爪部2の部分の転動体4(鋼
球)による損傷度合と鋼球の組み込み性を調べ、つぎに
示した判定基準に従って判定し、表−1に示す。(1) Assembling test at the time of assembly As shown in FIG.
The degree of damage by the rolling element 4 (steel ball) in the portion of the claw portion 2 of the cage 1 and the assembling property of the steel ball are examined, and the determination is made according to the following criteria.
保持器の爪の部分の損傷度合: ○……全く損傷しない △……少し損傷する ×……かなり損傷する 鋼球の組み込み性: ○……組み込み時に無理なく組み込める △……組み込み時に少し抵抗がある ×……組み込み時にかなり抵抗がある (2)保持器の爪部の耐久試験 第3図に示すように、保持器1のポケット部3に球部
6の径が直径7.16mmである鋼球を備えた棒7を試験機8
によって50回/分の速さで出し入れさせて、保持器1の
爪部2が破損するまでの出し入れ回数を測定し、その値
を表−1に示す。この出し入れ回数が多い程、保持器1
の爪部2の疲労強度は大きく、製造工程において保持器
1の転動体4を組み込む際の安全率は高いといえる。Degree of damage to the claw part of the cage: ○ …… No damage at all △ …… Slight damage × …… Severe damage Assembleability of steel ball: ○ …… Easy to mount during assembly △ …… Slight resistance during assembly Yes × There is considerable resistance when assembled (2) Durability test of cage claws As shown in Fig. 3, a steel ball with a diameter of ball 6 in pocket 3 of cage 1 is 7.16 mm. A rod 7 equipped with a tester 8
The number of times of withdrawal and withdrawal until the claw portion 2 of the retainer 1 was damaged was measured by taking out and withdrawing at a speed of 50 times / min, and the value is shown in Table-1. The higher the number of times of taking in and out, the cage 1
It can be said that the claw portion 2 has a large fatigue strength and a safety factor when the rolling element 4 of the cage 1 is incorporated in the manufacturing process is high.
(3)保持器の変形率測定試験 潤滑剤(日本石油社製:ウレア系グリース、U295)を
0.8g封入し、フッ素ゴムにてシールをした軸受6203を運
転試験機にて、回転数15000rpmスラスト荷重6.8kgf、温
度220℃の条件で200時間運転し、保持器外径の寸法変形
率を測定し表−1に示す。この寸法変形率が小さい程保
持器は、変形していないことを示す。(3) Deformation rate measurement test of cage Use lubricant (Nippon Oil Co., Ltd .: urea grease, U295)
A bearing 6203 sealed with 0.8 g and sealed with fluororubber was operated for 200 hours under the conditions of a rotational speed of 15000 rpm, a thrust load of 6.8 kgf, and a temperature of 220 ° C with an operating tester to measure the dimensional deformation rate of the cage outer diameter. The results are shown in Table-1. A smaller dimensional deformation rate indicates that the cage is not deformed.
(4)保持器の劣化度合判定試験 試験(3)と全く同様の条件で200時間継続運転後の
潤滑剤(日本石油社製:ウレア系グリース、U295)の劣
化度合を判定し、第1表に併記した。(4) Cage Deterioration Degree Judgment Test Deterioration degree of the lubricant (Urea grease, U295 manufactured by Nippon Oil Co., Ltd.) after 200 hours of continuous operation was judged under exactly the same conditions as in Test (3), and Table 1 was used. Also described in.
○……変色有り、劣化なし △……変色有り、少し劣化なし ×……変色有り、かなり劣化している (5)熱変形温度 機械的分析装置(島津製作所製TM−30)を用いて、昇
温速度毎分5℃、圧力18.6kgf/cm2としたTMA針入法によ
る針入開始温度から求めた(ASTM D 648に準拠する)。○ …… Discoloration, no deterioration △ …… Discoloration, little deterioration × …… Discoloration, considerably deteriorated (5) Thermal deformation temperature Using a mechanical analyzer (TM-30 manufactured by Shimadzu Corporation) It was determined from the penetration start temperature by the TMA penetration method with a temperature rising rate of 5 ° C./min and a pressure of 18.6 kgf / cm 2 (based on ASTM D 648).
比較例1〜3 熱可塑性ポリイミドの代りにPAIをベース樹脂として
使用した以外は実施例と同様に、表−1に示す割合でヘ
ンシェルミキサーを用いて乾式混合し、二軸溶融押出器
に供給し、シリンダー温度340〜350℃、スクリュー回転
数50〜100rpmの条件にて溶融混合および造粒をした。そ
の後シリンダー温度340〜360℃、金型温度160〜210℃、
射出圧力500〜1000kg/cm2の条件にて第1図に示したよ
うな軸受6203の保持器1を射出成形し、実施例と同様の
試験を行なった。Comparative Examples 1 to 3 Dry mixing was performed using a Henschel mixer in the proportions shown in Table 1 in the same manner as in Examples except that PAI was used as the base resin instead of the thermoplastic polyimide, and the mixture was supplied to the twin-screw extruder. Melt mixing and granulation were performed under the conditions of a cylinder temperature of 340 to 350 ° C and a screw rotation speed of 50 to 100 rpm. After that, the cylinder temperature is 340-360 ℃, the mold temperature is 160-210 ℃,
The cage 1 of the bearing 6203 as shown in FIG. 1 was injection-molded under the condition of injection pressure of 500 to 1000 kg / cm 2 , and the same test as the example was conducted.
比較例4〜5 熱可塑性ポリイミドの代りにPPSをベース樹脂として
使用した以外は実施例と同様に、表−1に示す割合でヘ
ンシェルミキサーを用いて乾式混合し、二軸溶融押出機
に供給し、シリンダー温度270〜330℃、スクリュー回転
数50〜100rpmの条件にて溶融混合および造粒をした。そ
の後シリンダー温度280〜340℃、金型温度100〜150℃、
射出圧力500〜1000kg/cm2の条件にて第1図に示したよ
うに軸受6203の保持器1を射出成形し、実施例と同様の
試験を行なった。Comparative Examples 4 to 5 In the same manner as in Example except that PPS was used as the base resin instead of the thermoplastic polyimide, dry mixing was performed using a Henschel mixer in the proportions shown in Table-1, and the mixture was supplied to the twin-screw extruder. Melt mixing and granulation were performed under the conditions of a cylinder temperature of 270 to 330 ° C. and a screw rotation speed of 50 to 100 rpm. After that, cylinder temperature 280-340 ℃, mold temperature 100-150 ℃,
The cage 1 of the bearing 6203 was injection-molded as shown in FIG. 1 under the condition of injection pressure of 500 to 1000 kg / cm 2 , and the same test as in the example was conducted.
比較例6 熱硬化性ポリイミド樹脂(デュポン社製、商品名:VES
PEL SP 21)の棒材を購入し、これを切削加工すること
によって切削加工し、第1図に示したような軸受6203の
保持器1を得、同様な試験を行なった。Comparative Example 6 Thermosetting Polyimide Resin (manufactured by DuPont, trade name: VES
A bar material of PEL SP 21) was purchased and cut by cutting this to obtain a retainer 1 of a bearing 6203 as shown in FIG. 1, and the same test was performed.
比較例7〜8 合成例1の熱可塑性ポリイミド樹脂をベースに表−1
に示す割合で、特にチタン酸カリウム繊維(大塚化学
(株)製、商品名TISMO)を配合した事以外は、実施例
1と同様にして射出成形して、同様の試験を行った。結
果を表−1に示す。Comparative Examples 7-8 Table 1 based on the thermoplastic polyimide resin of Synthesis Example 1
The same test was carried out by injection molding in the same manner as in Example 1 except that potassium titanate fiber (manufactured by Otsuka Chemical Co., Ltd., trade name TISMO) was blended in the proportion shown in. The results are shown in Table 1.
表−1に示す結果から明らかなように、熱可塑性ポリ
イミドからなる実施例1〜3の保持器は組立て時の組み
込み性や爪部の耐久性に優れ、しかも高温で運転される
軸受内にあって変形率は低く、潤滑剤を劣化させたり、
保持器自身が劣化することがない。 As is clear from the results shown in Table 1, the cages of Examples 1 to 3 made of thermoplastic polyimide have excellent assemblability at the time of assembly and durability of the claw portion, and are in a bearing operated at high temperature. The deformation rate is low, which may deteriorate the lubricant,
The cage itself does not deteriorate.
それに比較してPAIからなる比較例1〜3の保持器、P
PSからなる比較例4,5の保持器はいずれも運転試験後の
変形率が大きく、潤滑剤、保持器自身も劣化していた。
また、切削加工より作製した比較例6の保持器は、組み
込み性および爪の耐久性に劣っていた。In comparison, the cage of Comparative Examples 1 to 3 made of PAI, P
The cages of Comparative Examples 4 and 5 made of PS all had a large deformation rate after the operation test, and the lubricant and the cage themselves were deteriorated.
Further, the cage of Comparative Example 6 produced by cutting was inferior in assembling property and nail durability.
爪の耐久性に劣っていた。また、チタン酸カリウム繊
維を多量含有する比較例7〜8の保持器も、爪の損傷、
組み込み性、耐久性、保持器自体の変形、劣化において
劣る傾向にあった。The nails were inferior in durability. Further, the cages of Comparative Examples 7 to 8 containing a large amount of potassium titanate fibers also showed damage to the nails,
It tended to be inferior in terms of ease of installation, durability, deformation and deterioration of the cage itself.
以上の説明からも明らかなように、この発明の保持器
は、柔軟性を有して軸受への組み込み性が良好で、高温
で使用した場合でも変形率が低いので軸受が損傷せず、
しかも耐熱性、耐薬品性、射出成形性をも兼ね備えたも
のである。この発明の保持器の利用分野は極めて広く、
自動者関連業界、一般機器関連業界、電機電子関連業
界、その他多くの分野で用いられる軸受用保持器として
最適のものである。As is clear from the above description, the cage of the present invention has flexibility and is easily incorporated into the bearing, and the deformation rate is low even when used at high temperatures, so the bearing is not damaged,
Moreover, it also has heat resistance, chemical resistance, and injection moldability. The field of use of the cage of the present invention is extremely wide,
It is most suitable as a bearing retainer used in a number of fields such as automatic machinery related industries, general equipment related industries, electrical and electronic related industries and many other fields.
第1図は転がり軸受用保持器の要部を例示する斜視図、
第2図は鋼球の組み込み性を調べるための転がり軸受用
保持器と軸受との関係を示す断面図、第3図は転がり軸
受用保持器の爪部の耐久試験を説明する試験機の平面図
である。 1……転がり軸受用保持器 2……爪部、3……ポケット部 4……転動体、5……軸受本体FIG. 1 is a perspective view illustrating a main part of a rolling bearing cage,
FIG. 2 is a cross-sectional view showing the relationship between the rolling bearing cage and the bearing for investigating the assemblability of steel balls, and FIG. 3 is the plane of a testing machine for explaining the durability test of the claw portion of the rolling bearing cage. It is a figure. 1 ... Roller bearing cage 2 ... Claws, 3 ... Pockets 4 ... Rolling elements, 5 ... Bearing body
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 F16C 33/44 F16C 33/44 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI technical display location F16C 33/44 F16C 33/44
Claims (1)
よりなるポリイミド系樹脂組成物からなり、当該ポリイ
ミド樹脂が下記一般式 で示される繰り返し単位からなる熱可塑性ポリイミド樹
脂であって、該熱可塑性ポリイミド樹脂粉末0.5gを100m
lのp−クロロフェノール/フェノール混合溶媒(混合
重量比90:10)に加熱溶解した溶液の35℃における溶液
粘度が0.35〜0.80dl/gであり、かつ、該ポリイミド系樹
脂組成物の総量中に、(i)5〜50重量%のフッ素樹
脂、黒鉛及び二硫化モリブデンより選ばれた少なくとも
1種の潤滑剤及び(ii)0〜50重量%のガラス繊維、カ
ーボン繊維、ボロン繊維、炭化ケイ素繊維、カーボンウ
イスカー、アスベスト、金属繊維及びロックウールより
選ばれた少なくとも1種の繊維状補強剤からなる添加剤
を含み、かつ該添加剤(i)(ii)の合計量が5〜60重
量%であることを特徴とする軸受用プラスチック保持
器。1. A polyimide resin composition comprising a polyimide resin, a lubricant and a fibrous reinforcing agent, wherein the polyimide resin has the following general formula: A thermoplastic polyimide resin consisting of repeating units represented by 100 g of the thermoplastic polyimide resin powder 0.5 g
of p-chlorophenol / phenol mixed solvent (mixing weight ratio: 90:10) having a solution viscosity at 35 ° C. of 0.35 to 0.80 dl / g, and in the total amount of the polyimide resin composition. And (i) 5 to 50% by weight of a fluororesin, at least one lubricant selected from graphite and molybdenum disulfide, and (ii) 0 to 50% by weight of glass fiber, carbon fiber, boron fiber, silicon carbide. An additive comprising at least one fibrous reinforcing agent selected from fibers, carbon whiskers, asbestos, metal fibers and rock wool, and the total amount of the additives (i) and (ii) is 5 to 60% by weight. A plastic retainer for bearings, characterized in that
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1326089A JP2525490B2 (en) | 1989-12-18 | 1989-12-18 | Plastic cage for bearing |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1326089A JP2525490B2 (en) | 1989-12-18 | 1989-12-18 | Plastic cage for bearing |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH03188127A JPH03188127A (en) | 1991-08-16 |
JP2525490B2 true JP2525490B2 (en) | 1996-08-21 |
Family
ID=18183984
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1326089A Expired - Lifetime JP2525490B2 (en) | 1989-12-18 | 1989-12-18 | Plastic cage for bearing |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2525490B2 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2584936Y2 (en) * | 1992-08-19 | 1998-11-11 | 日本精工株式会社 | Ball bearings for turbochargers |
CN112795187A (en) * | 2020-12-29 | 2021-05-14 | 长沙新材料产业研究院有限公司 | Polyimide bearing retainer material and preparation method thereof |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6037417A (en) * | 1983-08-10 | 1985-02-26 | Otsuka Chem Co Ltd | Plastic retainer |
JPH0615623B2 (en) * | 1987-10-26 | 1994-03-02 | 三井東圧化学株式会社 | Heat treatment method for polyimide molding |
-
1989
- 1989-12-18 JP JP1326089A patent/JP2525490B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH03188127A (en) | 1991-08-16 |
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