JPH04362311A - Retainer for rolling bearing - Google Patents
Retainer for rolling bearingInfo
- Publication number
- JPH04362311A JPH04362311A JP13276791A JP13276791A JPH04362311A JP H04362311 A JPH04362311 A JP H04362311A JP 13276791 A JP13276791 A JP 13276791A JP 13276791 A JP13276791 A JP 13276791A JP H04362311 A JPH04362311 A JP H04362311A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- elastomer
- aromatic ring
- cage
- polyamide
- 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
- 238000005096 rolling process Methods 0.000 title claims abstract description 13
- 229920001971 elastomer Polymers 0.000 claims abstract description 24
- 239000000806 elastomer Substances 0.000 claims abstract description 23
- 125000003118 aryl group Chemical group 0.000 claims abstract description 21
- 229920002647 polyamide Polymers 0.000 claims description 20
- 239000004952 Polyamide Substances 0.000 claims description 19
- 239000012783 reinforcing fiber Substances 0.000 claims description 11
- 239000000835 fiber Substances 0.000 abstract description 7
- 239000010687 lubricating oil Substances 0.000 abstract description 5
- 229920003002 synthetic resin Polymers 0.000 abstract description 2
- 239000000057 synthetic resin Substances 0.000 abstract description 2
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 description 24
- 238000009472 formulation Methods 0.000 description 20
- 239000012778 molding material Substances 0.000 description 18
- 239000003365 glass fiber Substances 0.000 description 12
- 150000001875 compounds Chemical class 0.000 description 11
- 239000003921 oil Substances 0.000 description 11
- 238000012360 testing method Methods 0.000 description 9
- 230000007423 decrease Effects 0.000 description 7
- 239000004953 Aliphatic polyamide Substances 0.000 description 6
- 229920003231 aliphatic polyamide Polymers 0.000 description 6
- 230000000694 effects Effects 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000004677 Nylon Substances 0.000 description 3
- 229920002302 Nylon 6,6 Polymers 0.000 description 3
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 229920002292 Nylon 6 Polymers 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 239000012208 gear oil Substances 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 2
- 238000007655 standard test method Methods 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- 229920003189 Nylon 4,6 Polymers 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 229920003469 Ultramid® T Polymers 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920006231 aramid fiber Polymers 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 238000009863 impact test Methods 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 229920003049 isoprene rubber Polymers 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 239000000615 nonconductor Substances 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 239000002990 reinforced plastic Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 0.000 description 1
Landscapes
- Rolling Contact Bearings (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、転がり軸受用の保持器
に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a cage for rolling bearings.
【0002】0002
【従来の技術と発明が解決しようとする課題】従来、上
記保持器として、金属製のものに比べて軽量で、しかも
機械的特性に優れた、ナイロン6、ナイロン66等の脂
肪族系のポリアミドからなるものが多用されている。し
かし、上記脂肪族ポリアミドは、特に、自動車のトラン
スミッションの転がり軸受等において、高温の潤滑油中
で使用する際の耐性(耐油性)が不十分であり、120
〜130℃程度が限界で、それ以上の高温では、依然と
して、金属製の保持器を使用しなければならないのが現
状であった。[Prior Art and Problems to be Solved by the Invention] Conventionally, aliphatic polyamides such as nylon 6 and nylon 66, which are lighter than metal cages and have excellent mechanical properties, have been used as cages. Consisting of are often used. However, the aliphatic polyamide has insufficient resistance (oil resistance) when used in high-temperature lubricating oil, especially in rolling bearings of automobile transmissions, etc.
The current limit is about ~130°C, and at higher temperatures, it is still necessary to use a metal cage.
【0003】本発明は、以上の事情に鑑みてなされたも
のであって、特に、高温の潤滑油中で使用する際の耐性
に優れた、合成樹脂製の転がり軸受用保持器を提供する
ことを目的としている。The present invention has been made in view of the above circumstances, and it is an object of the present invention to provide a cage for a rolling bearing made of synthetic resin that has excellent resistance particularly when used in high-temperature lubricating oil. It is an object.
【0004】0004
【課題を解決するための手段および作用】上記の目的を
達成するため、本発明者らは、線状の脂肪族ポリアミド
の主鎖中に芳香族環を導入することで、通常の脂肪族ポ
リアミドより機械的特性や耐熱性を向上させたポリアミ
ド(以下「芳香族環含有ポリアミド」という)の使用を
検討した。この芳香族環含有ポリアミドは、柔軟性に欠
け、耐衝撃性が低いため割れ易いという欠点があり、し
かも、耐油性が不十分で、高温の潤滑油中で使用した際
の強度低下も著しいので、従来は、保持器への適用が不
可能であると考えられてきたものである。[Means and Effects for Solving the Problems] In order to achieve the above object, the present inventors have introduced an aromatic ring into the main chain of a linear aliphatic polyamide. We investigated the use of polyamide with improved mechanical properties and heat resistance (hereinafter referred to as "aromatic ring-containing polyamide"). This aromatic ring-containing polyamide lacks flexibility and has low impact resistance, making it easy to crack.Furthermore, it has insufficient oil resistance, and its strength decreases significantly when used in high-temperature lubricating oil. , which has conventionally been thought to be impossible to apply to cages.
【0005】しかし、本発明者らが鋭意研究を行った結
果、上記芳香族環含有ポリアミドにエラストマーおよび
強化繊維を配合すれば、靱性、機械的強度、耐油性等の
特性を全て向上できるとの知見を得、エラストマーおよ
び強化繊維の配合割合等についてさらに検討を行った結
果、本発明を完成するに至った。すなわち、本発明の転
がり軸受用保持器は、芳香族環含有ポリアミドと、エラ
ストマーと、強化繊維とを含有し、全成分中に占めるエ
ラストマーの割合が5〜20重量%、強化繊維の割合が
8〜30重量%の範囲内であることを特徴とする。However, as a result of intensive research by the present inventors, it was found that by blending an elastomer and reinforcing fibers into the aromatic ring-containing polyamide, all properties such as toughness, mechanical strength, and oil resistance can be improved. As a result of obtaining this knowledge and conducting further studies on the blending ratio of the elastomer and reinforcing fibers, etc., the present invention was completed. That is, the rolling bearing cage of the present invention contains an aromatic ring-containing polyamide, an elastomer, and reinforcing fibers, and the ratio of the elastomer to the total components is 5 to 20% by weight, and the ratio of the reinforcing fibers is 8% by weight. It is characterized by being within the range of ~30% by weight.
【0006】芳香族環含有ポリアミドとしては、前述し
たように、ナイロン6、ナイロン66、ナイロン46等
の、線状の脂肪族ポリアミド(ナイロン)の主鎖中に芳
香族環を導入した化合物が好適に使用される。これらの
化合物は、ナイロンの持つ成形性の良さ等の特性を失う
ことなく、しかも、ナイロンより機械的特性に優れてい
るとともに、耐熱性も向上している。As the aromatic ring-containing polyamide, as mentioned above, compounds in which an aromatic ring is introduced into the main chain of a linear aliphatic polyamide (nylon), such as nylon 6, nylon 66, and nylon 46, are suitable. used for. These compounds do not lose the properties of nylon, such as good moldability, and have better mechanical properties and improved heat resistance than nylon.
【0007】上記芳香族環含有ポリアミドの最も好適な
例としては、BASF社製の商品名ウルトラミッドTが
挙げられる。この化合物は、カプロラクタムとヘキサメ
チレンジアミンとテレフタル酸とを反応させてなるもの
で、下記一般式(I) において左側に示すカプロラク
タム部分と、右側に示すヘキサメチレンジアミン−テレ
フタル酸部分とがランダムに結合した、ランダムコポリ
マーの構造を有している。The most preferred example of the aromatic ring-containing polyamide is Ultramid T, a trade name manufactured by BASF. This compound is made by reacting caprolactam, hexamethylene diamine, and terephthalic acid, and in the general formula (I) below, the caprolactam moiety shown on the left and the hexamethylene diamine-terephthalic acid moiety shown on the right are randomly bonded. It has a random copolymer structure.
【0008】[0008]
【化1】
エラストマーとしては、天然ゴム;ブタジエンゴム、イ
ソプレンゴム、スチレン−ブタジエンゴム、アクリロニ
トリルブタジエンゴム、クロロプレンゴム、エチレン−
プロピレンゴム等の合成ゴム;スチレン系、オレフィン
系、ウレタン系、ポリエステル系、ポリアミド系、ポリ
塩化ビニル系等の熱可塑性エラストマーが例示される。[Chemical 1] Elastomers include natural rubber; butadiene rubber, isoprene rubber, styrene-butadiene rubber, acrylonitrile-butadiene rubber, chloroprene rubber, ethylene-butadiene rubber,
Synthetic rubbers such as propylene rubber; thermoplastic elastomers such as styrene-based, olefin-based, urethane-based, polyester-based, polyamide-based, and polyvinyl chloride-based are exemplified.
【0009】全成分中に占めるエラストマーの割合は、
5〜20重量%の範囲内に限定される。エラストマーの
割合が5重量%未満では、当該エラストマーの添加効果
が得られず耐油性が低下し、エラストマーの割合が20
重量%を上回ると、相対的に芳香族環含有ポリアミドの
割合が減少するので、機械的特性が悪化するとともに、
耐熱性が低下する。[0009] The proportion of elastomer in all components is
It is limited within the range of 5 to 20% by weight. If the proportion of the elastomer is less than 5% by weight, the effect of adding the elastomer will not be obtained and the oil resistance will decrease, and if the proportion of the elastomer is less than 20% by weight, the oil resistance will decrease.
If it exceeds % by weight, the proportion of aromatic ring-containing polyamide decreases relatively, resulting in deterioration of mechanical properties and
Heat resistance decreases.
【0010】上記芳香族環含有ポリアミドおよびエラス
トマーは、それぞれ単体のものを混合して使用できる他
、両者のブロック共重合体、グラフト共重合体を使用す
ることもできる。強化繊維としては、ガラス繊維、炭素
繊維、繊維状の珪灰石(ウォラストナイト)、炭化ケイ
素繊維、ボロン繊維、アルミナ繊維、Si−Ti−C−
O繊維、金属繊維(銅、鋼、ステンレス鋼等)、芳香族
ポリアミド(アラミド)繊維、チタン酸カリウムウイス
カー、グラファイトウイスカー、炭化ケイ素ウイスカー
、窒化ケイ素ウイスカー、アルミナウイスカー等が例示
される。The above-mentioned aromatic ring-containing polyamide and elastomer can be used alone as a mixture, or as a block copolymer or a graft copolymer of the two. Examples of reinforcing fibers include glass fiber, carbon fiber, fibrous wollastonite, silicon carbide fiber, boron fiber, alumina fiber, Si-Ti-C-
Examples include O fibers, metal fibers (copper, steel, stainless steel, etc.), aromatic polyamide (aramid) fibers, potassium titanate whiskers, graphite whiskers, silicon carbide whiskers, silicon nitride whiskers, alumina whiskers, and the like.
【0011】全成分中に占める強化繊維の割合は、8〜
30重量%の範囲内に限定される。強化繊維の割合が8
重量%未満では、当該強化繊維の添加効果が得られず、
靱性が悪化するとともに、耐熱性が低下する。一方、強
化繊維の割合が30重量%を上回ると、柔軟性が低下し
て、特に、アンダーカットになった形状の場合に、例え
ば金型から成形品を抜き取ったり、ポケットに転動体を
圧入したりすることで、上記アンダーカットの部分に割
れやクラックが発生する。[0011] The proportion of reinforcing fibers in all components is 8 to 8.
It is limited within the range of 30% by weight. The ratio of reinforcing fibers is 8
If it is less than % by weight, the effect of adding the reinforcing fiber cannot be obtained,
Toughness deteriorates and heat resistance decreases. On the other hand, if the proportion of reinforcing fibers exceeds 30% by weight, the flexibility decreases, especially in the case of an undercut shape, for example, when the molded product is removed from the mold or the rolling elements are press-fitted into the pocket. This causes cracks and cracks to occur in the undercut portion.
【0012】本発明の転がり軸受用保持器は、上記の各
成分を溶融混練し、ペレット状、粉末状等の、成形材料
として使用可能な形状にした後、従来と同様に、射出成
形機等を用いて成形することで製造される。本発明の構
成は、玉軸受、針状ころ軸受、円筒ころ軸受、円錐ころ
軸受等の種々の転がり軸受用の、あらゆる形状の保持器
に適用することができ、特に、アンダーカットを有する
形状の保持器に好適に適用することができる。The cage for rolling bearings of the present invention is produced by melting and kneading the above-mentioned components to form pellets, powders, or other forms that can be used as molding materials, and then processing the cages in an injection molding machine, etc. in the same manner as in the past. It is manufactured by molding using. The structure of the present invention can be applied to cages of all shapes for various rolling bearings such as ball bearings, needle roller bearings, cylindrical roller bearings, tapered roller bearings, etc., and in particular cages of shapes with undercuts. It can be suitably applied to a cage.
【0013】[0013]
【実施例】下記の各配合例の成形材料を用いて、後述す
る各試験を行った。
<配合例>
配合例1
芳香族環含有ポリアミドとしての、前記一般式(I)
で表される化合物85重量%、エラストマー5重量%お
よびガラス繊維10重量%を含有する成形材料。[Example] Using the molding materials of the following formulation examples, the tests described below were conducted. <Blend Example> Blend Example 1 The above general formula (I) as an aromatic ring-containing polyamide
A molding material containing 85% by weight of a compound represented by: 5% by weight of an elastomer and 10% by weight of glass fibers.
【0014】配合例2
芳香族環含有ポリアミドとしての、前記一般式(I)
で表される化合物70重量%、エラストマー10重量%
およびガラス繊維20重量%を含有する成形材料。
配合例3
芳香族環含有ポリアミドとしての、前記一般式(I)
で表される化合物50重量%、エラストマー20重量%
およびガラス繊維30重量%を含有する成形材料。Formulation Example 2 The above general formula (I) as an aromatic ring-containing polyamide
70% by weight of the compound represented by, 10% by weight of the elastomer
and a molding material containing 20% by weight of glass fibers. Formulation Example 3 The above general formula (I) as an aromatic ring-containing polyamide
50% by weight of the compound represented by, 20% by weight of the elastomer
and a molding material containing 30% by weight of glass fibers.
【0015】配合例4
芳香族環含有ポリアミドとしての、前記一般式(I)
で表される化合物のみからなる成形材料。
配合例5
芳香族環含有ポリアミドとしての、前記一般式(I)
で表される化合物75重量%およびガラス繊維25重量
%を含有する成形材料。Formulation Example 4 The above general formula (I) as an aromatic ring-containing polyamide
A molding material consisting only of the compound represented by. Formulation Example 5 The above general formula (I) as aromatic ring-containing polyamide
A molding material containing 75% by weight of the compound represented by and 25% by weight of glass fibers.
【0016】配合例6
芳香族環含有ポリアミドとしての、前記一般式(I)
で表される化合物80重量%およびエラストマー20重
量%を含有する成形材料。
配合例7
芳香族環含有ポリアミドとしての、前記一般式(I)
で表される化合物50重量%、エラストマー10重量%
およびガラス繊維40重量%を含有する成形材料。Formulation Example 6 The above general formula (I) as aromatic ring-containing polyamide
A molding material containing 80% by weight of a compound represented by and 20% by weight of an elastomer. Formulation Example 7 The above general formula (I) as aromatic ring-containing polyamide
50% by weight of the compound represented by, 10% by weight of the elastomer
and a molding material containing 40% by weight of glass fibers.
【0017】配合例8
芳香族環含有ポリアミドとしての、前記一般式(I)
で表される化合物50重量%、エラストマー30重量%
およびガラス繊維20重量%を含有する成形材料。
配合例9
脂肪族ポリアミド(ナイロン66)75重量%およびガ
ラス繊維25重量%を含有する成形材料。
<試験>
引張試験
ASTM D 638−82a「Standard
Test Methodfor TENSILE P
ROPERTIES OF PLASTICS(プラス
チックの引張特性の試験方法)」に則って、上記各配合
例の成形材料の引張破断強度(kgf/cm2 )およ
び引張破断伸び(%)を測定した。なお、測定には、各
配合例の成形材料から作製した、TypeI試験片を用
いた。Formulation Example 8 The above general formula (I) as aromatic ring-containing polyamide
50% by weight of the compound represented by, 30% by weight of the elastomer
and a molding material containing 20% by weight of glass fibers. Formulation Example 9 Molding material containing 75% by weight of aliphatic polyamide (nylon 66) and 25% by weight of glass fibers. <Test> Tensile test ASTM D 638-82a "Standard
Test Method for TENSILE P
The tensile strength at break (kgf/cm2) and tensile elongation at break (%) of the molding materials of each of the above formulation examples were measured in accordance with ``ROPERTIES OF PLASTICS''. Note that, for the measurement, Type I test pieces prepared from the molding materials of each blending example were used.
【0018】曲げ試験
ASTM D 790−81「Standard
Test Method for FLEXURAL
PROPERTIES OF UNREINFORCE
D AND REINFORCED PLASTICS
AND ELECTRICAL INSULATIN
G MATERIALS(強化または未強化のプラスチ
ックおよび電気絶縁体の曲げ特性の試験方法)」に則っ
て、上記各配合例の成形材料の曲げ強度(kgf/cm
2 )を測定した。なお、測定には、各配合例の成形材
料から作製した、長さ5inch×幅1/2inch×
高さ1/4inchの試験片を用いた。Bending test ASTM D 790-81 "Standard"
Test Method for FLEXURAL
PROPERTIES OF UNREINFORCE
D AND REINFORCED PLASTICS
AND ELECTRICAL INSULATIN
The bending strength (kgf/cm
2) was measured. In addition, for the measurement, 5 inch length x 1/2 inch width x 1/2 inch width fabricated from the molding material of each formulation example.
A test piece with a height of 1/4 inch was used.
【0019】また、上記ASTM D 790の1
1.11項に記載の式により、曲げ弾性率(kgf/c
m2 )を算出した。
アイゾット衝撃試験
ASTM D 256−81「Standard
Test Method for IMPACT RE
SITANCEOF PLASTICS AND EL
ECTRICAL INSULATING MATER
IALS (プラスチックおよび電気絶縁体の耐衝撃特
性の試験方法)」に則って、上記各配合例の成形材料の
アイゾット衝撃強度(kgf・cm/cm)を測定した
。なお、測定には、各配合例の成形材料から作製した、
1/8inchの切欠きを有する試験片を用いた。[0019] Also, the above ASTM D 790-1
According to the formula described in Section 1.11, the flexural modulus (kgf/c
m2) was calculated. Izod impact test ASTM D 256-81 “Standard
Test Method for IMPACT RE
SITANCEOF PLASTICS AND EL
ECTRICAL INSULATION MATER
The Izod impact strength (kgf·cm/cm) of the molding materials of each of the above formulation examples was measured in accordance with ``IALS (Test Method for Impact Resistance Properties of Plastics and Electrical Insulators)''. In addition, for the measurement, the molding material made from the molding material of each formulation example,
A test piece with a 1/8 inch notch was used.
【0020】成形性試験
上記各配合例の成形材料をペレット化し、射出成形機を
用いて、外径57mm、内径50mm、幅34mm、ポ
ケット数27の針状ころ軸受用保持器の成形を行い、ア
ンダーカット部の割れやクラックの発生の有無を観察し
た。保持器強度測定
上記成形性試験において割れやクラックが発生しなかっ
た保持器をポケット2つ分だけ切断してサンプルSを作
製し、図1(a)(b)に示すように、各サンプルSの
ポケット11,11に一対の治具2,2の突起21,2
1を挿入した状態で、当該治具2,2を図中矢印で示す
ように上下に引っ張った際の、破断強度の初期値S1
(kgf)を測定した。Formability test The molding materials of each of the above compounding examples were pelletized, and using an injection molding machine, a cage for a needle roller bearing having an outer diameter of 57 mm, an inner diameter of 50 mm, a width of 34 mm, and a number of pockets of 27 was formed. The presence or absence of cracks or cracks in the undercut portion was observed. Measurement of Cage Strength Samples S were prepared by cutting the cage that did not show cracks or cracks in the above moldability test by two pockets. The protrusions 21, 2 of the pair of jigs 2, 2 are placed in the pockets 11, 11 of the
Initial value S1 of the breaking strength when the jigs 2, 2 are pulled up and down as shown by the arrows in the figure with 1 inserted.
(kgf) was measured.
【0021】次に、上記保持器を140℃のギヤ油中に
500時間(配合例9については、120℃のギヤ油中
に500時間)浸漬した後の、保持器の破断強度S2
(kgf)を、上記と同様にして測定した。さらに、上
記破断強度の初期値S1 と、耐熱後の破断強度S2
とから、下記式(1) により、破断強度の保持率RS
(%)を算出した。Next, the breaking strength S2 of the cage after immersing the cage in gear oil at 140° C. for 500 hours (for formulation example 9, 500 hours in gear oil at 120° C.)
(kgf) was measured in the same manner as above. Furthermore, the initial value S1 of the above-mentioned breaking strength and the breaking strength S2 after heat resistance are determined.
From the following formula (1), the retention rate of breaking strength RS
(%) was calculated.
【0022】RS (%)=S2 /S1 ×100…
(1)以上の結果を表1および表2に示す。[0022]RS (%)=S2/S1×100...
(1) The above results are shown in Tables 1 and 2.
【0023】[0023]
【表1】[Table 1]
【0024】[0024]
【表2】
上記表1、表2の結果より、エラストマーおよびガラス
繊維を含有せず、芳香族環含有ポリアミド単独の配合例
4は、脆くかつ耐油性が悪いことが判った。また、エラ
ストマーを含有しない配合例5は、機械的特性に改善が
見られるが、依然として耐油性が悪く、逆に、ガラス繊
維を含有しない配合例6は、脆く、かつ耐油性も悪いこ
とが判った。[Table 2] From the results in Tables 1 and 2 above, it was found that Blend Example 4, which contained no elastomer or glass fiber and contained only aromatic ring-containing polyamide, was brittle and had poor oil resistance. In addition, Formulation Example 5, which does not contain elastomer, shows improvement in mechanical properties, but still has poor oil resistance.On the contrary, Formulation Example 6, which does not contain glass fiber, is brittle and has poor oil resistance. Ta.
【0025】ガラス繊維の含有割合が30重量%を上回
る配合例7は、柔軟性に欠け、成形性試験において割れ
、クラックが発生し、一方、エラストマーの含有割合が
20重量%を上回る配合例8は、脆く、かつ耐油性も悪
いことが判った。さらに、従来の、脂肪族ポリアミドと
ガラス繊維とからなる配合例9は、耐油性が著しく悪い
ことも判った。[0025] Formulation Example 7, in which the glass fiber content exceeds 30% by weight, lacks flexibility and cracks occur in the moldability test, while Formulation Example 8, in which the elastomer content exceeds 20% by weight. was found to be brittle and have poor oil resistance. Furthermore, it was also found that the conventional blending example 9 consisting of aliphatic polyamide and glass fiber had extremely poor oil resistance.
【0026】これに対し、本発明の転がり軸受用保持器
の成分配合である配合例1〜3は、いずれも、機械的特
性に優れているとともに、柔軟性、耐油性に優れている
ことが判明した。On the other hand, formulation examples 1 to 3, which are component formulations of the cage for rolling bearings of the present invention, all have excellent mechanical properties as well as flexibility and oil resistance. found.
【0027】[0027]
【発明の効果】本発明の転がり軸受用保持器は、以上の
ように構成されているため、特に、高温の潤滑油中で使
用する際の耐性に優れたものとなっている。[Effects of the Invention] Since the rolling bearing cage of the present invention is constructed as described above, it has excellent durability particularly when used in high-temperature lubricating oil.
【図1】同図(a)(b)は針状ころ軸受用保持器の強
度測定方法を示す説明図である。FIGS. 1(a) and 1(b) are explanatory diagrams showing a method for measuring the strength of a cage for a needle roller bearing.
Claims (1)
エラストマーと、強化繊維とを含有し、全成分中に占め
るエラストマーの割合が5〜20重量%、強化繊維の割
合が8〜30重量%の範囲内であることを特徴とする転
がり軸受用保持器。Claim 1: A polyamide having an aromatic ring in its main chain;
A cage for rolling bearings containing an elastomer and reinforcing fibers, wherein the proportion of the elastomer in the total components is within the range of 5 to 20% by weight, and the proportion of the reinforcing fibers is within the range of 8 to 30% by weight. .
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP03132767A JP3128264B2 (en) | 1991-06-04 | 1991-06-04 | Cage for rolling bearing |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP03132767A JP3128264B2 (en) | 1991-06-04 | 1991-06-04 | Cage for rolling bearing |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04362311A true JPH04362311A (en) | 1992-12-15 |
JP3128264B2 JP3128264B2 (en) | 2001-01-29 |
Family
ID=15089080
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP03132767A Expired - Lifetime JP3128264B2 (en) | 1991-06-04 | 1991-06-04 | Cage for rolling bearing |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3128264B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006019121A1 (en) * | 2004-08-17 | 2006-02-23 | Jtekt Corporation | Bearing retainer |
JP2007321815A (en) * | 2006-05-30 | 2007-12-13 | Nsk Ltd | Linear motion device |
CN102993738A (en) * | 2012-08-22 | 2013-03-27 | 常熟市筑紫机械有限公司 | Preparation method of nylon composite material filled with nano silicon nitride |
-
1991
- 1991-06-04 JP JP03132767A patent/JP3128264B2/en not_active Expired - Lifetime
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006019121A1 (en) * | 2004-08-17 | 2006-02-23 | Jtekt Corporation | Bearing retainer |
JPWO2006019121A1 (en) * | 2004-08-17 | 2008-05-08 | 株式会社ジェイテクト | Bearing cage |
JP2007321815A (en) * | 2006-05-30 | 2007-12-13 | Nsk Ltd | Linear motion device |
JP4730209B2 (en) * | 2006-05-30 | 2011-07-20 | 日本精工株式会社 | Linear motion equipment |
CN102993738A (en) * | 2012-08-22 | 2013-03-27 | 常熟市筑紫机械有限公司 | Preparation method of nylon composite material filled with nano silicon nitride |
Also Published As
Publication number | Publication date |
---|---|
JP3128264B2 (en) | 2001-01-29 |
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