JPH0396716A - Race for roller bearing - Google Patents
Race for roller bearingInfo
- Publication number
- JPH0396716A JPH0396716A JP2166243A JP16624390A JPH0396716A JP H0396716 A JPH0396716 A JP H0396716A JP 2166243 A JP2166243 A JP 2166243A JP 16624390 A JP16624390 A JP 16624390A JP H0396716 A JPH0396716 A JP H0396716A
- Authority
- JP
- Japan
- Prior art keywords
- pps resin
- cage
- poise
- race
- resin
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 229920005989 resin Polymers 0.000 claims abstract description 68
- 239000011347 resin Substances 0.000 claims abstract description 68
- 238000005096 rolling process Methods 0.000 claims abstract description 19
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 12
- 239000004734 Polyphenylene sulfide Substances 0.000 claims description 36
- 229920000069 polyphenylene sulfide Polymers 0.000 claims description 36
- 239000000155 melt Substances 0.000 claims description 15
- 238000004132 cross linking Methods 0.000 claims description 11
- 239000012779 reinforcing material Substances 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 4
- 239000000463 material Substances 0.000 abstract description 7
- 229910000831 Steel Inorganic materials 0.000 abstract description 6
- 239000010959 steel Substances 0.000 abstract description 6
- 239000000126 substance Substances 0.000 abstract description 6
- 239000006085 branching agent Substances 0.000 abstract description 3
- 239000003431 cross linking reagent Substances 0.000 abstract description 3
- 238000010438 heat treatment Methods 0.000 abstract description 3
- 238000002844 melting Methods 0.000 abstract description 3
- 230000008018 melting Effects 0.000 abstract description 3
- 238000000034 method Methods 0.000 abstract description 3
- 230000002787 reinforcement Effects 0.000 abstract description 3
- 239000002131 composite material Substances 0.000 abstract description 2
- 238000001746 injection moulding Methods 0.000 abstract description 2
- 238000002156 mixing Methods 0.000 abstract description 2
- 230000004927 fusion Effects 0.000 abstract 1
- 239000011148 porous material Substances 0.000 abstract 1
- 230000000717 retained effect Effects 0.000 abstract 1
- 238000003466 welding Methods 0.000 abstract 1
- 239000000835 fiber Substances 0.000 description 11
- 238000012360 testing method Methods 0.000 description 10
- 210000000078 claw Anatomy 0.000 description 9
- 239000003365 glass fiber Substances 0.000 description 8
- 239000011521 glass Substances 0.000 description 7
- 230000006866 deterioration Effects 0.000 description 5
- 239000000314 lubricant Substances 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 239000004677 Nylon Substances 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 229920001778 nylon Polymers 0.000 description 4
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 238000002845 discoloration Methods 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 229910002804 graphite Inorganic materials 0.000 description 3
- 239000010439 graphite Substances 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 3
- 229910010271 silicon carbide Inorganic materials 0.000 description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 229920000049 Carbon (fiber) Polymers 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 239000000292 calcium oxide Substances 0.000 description 2
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 239000004917 carbon fiber Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000004519 grease Substances 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- JKQOBWVOAYFWKG-UHFFFAOYSA-N molybdenum trioxide Chemical compound O=[Mo](=O)=O JKQOBWVOAYFWKG-UHFFFAOYSA-N 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 229920006122 polyamide resin Polymers 0.000 description 2
- 239000004810 polytetrafluoroethylene Substances 0.000 description 2
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 2
- 238000004513 sizing Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- WUPHOULIZUERAE-UHFFFAOYSA-N 3-(oxolan-2-yl)propanoic acid Chemical compound OC(=O)CCC1CCCO1 WUPHOULIZUERAE-UHFFFAOYSA-N 0.000 description 1
- 229910052580 B4C Inorganic materials 0.000 description 1
- 235000010893 Bischofia javanica Nutrition 0.000 description 1
- 240000005220 Bischofia javanica Species 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 239000005069 Extreme pressure additive Substances 0.000 description 1
- 239000004610 Internal Lubricant Substances 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- 239000002033 PVDF binder Substances 0.000 description 1
- 239000004695 Polyether sulfone Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 229910052980 cadmium sulfide Inorganic materials 0.000 description 1
- UHYPYGJEEGLRJD-UHFFFAOYSA-N cadmium(2+);selenium(2-) Chemical compound [Se-2].[Cd+2] UHYPYGJEEGLRJD-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 229910001634 calcium fluoride Inorganic materials 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000007580 dry-mixing Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000010696 ester oil Substances 0.000 description 1
- 229920000840 ethylene tetrafluoroethylene copolymer Polymers 0.000 description 1
- -1 fluororesin Substances 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229940064639 minipress Drugs 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 1
- 229910052982 molybdenum disulfide Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920001643 poly(ether ketone) Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 239000009719 polyimide resin Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 229920001955 polyphenylene ether Polymers 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- WFXFYZULCQKPIP-UHFFFAOYSA-N prazosin hydrochloride Chemical compound [H+].[Cl-].N=1C(N)=C2C=C(OC)C(OC)=CC2=NC=1N(CC1)CCN1C(=O)C1=CC=CO1 WFXFYZULCQKPIP-UHFFFAOYSA-N 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 229910052594 sapphire Inorganic materials 0.000 description 1
- 239000010980 sapphire Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- TXDNPSYEJHXKMK-UHFFFAOYSA-N sulfanylsilane Chemical compound S[SiH3] TXDNPSYEJHXKMK-UHFFFAOYSA-N 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical group [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
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
- F16C33/44—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
- 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2065/00—Use of polyphenylenes or polyxylylenes as moulding material
-
- 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
- F16C2208/52—Polyphenylene sulphide [PPS]
Landscapes
- Engineering & Computer Science (AREA)
- General Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Rolling Contact Bearings (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
この発明は高温下で使用できるプラスチック製の転がり
軸受用保持器に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] This invention relates to a cage for a rolling bearing made of plastic that can be used at high temperatures.
周知のように、プラスチック製の転がり軸受用保持器(
以下、保持器という)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ボリアミド系
樹脂を素材とする、いわゆるナイロン製の保持器が広く
用いられている。このような保持器1は、第1図にその
要部を示すように、上部に爪部2を有して出入口が狭小
のポケット部3に鋼球などの転勤体4を組み込んで回転
自在に保持するものである.
しかし、このナイロン製の保持器1は、120 ”C以
上の連続使用温度条件下、または、極圧添加剤その他が
添加された油類もしくはその他の酸性の薬剤と接触する
条件下では、ナイロンが劣化し、その特性を失うため良
好な状態で使用することができなかった.
このようなナイロンに代わる素材であって、高温条件下
で使用され、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樹脂と略称する)があり、
耐熱性とともに耐薬品性、戒形性などにも優れている.
このPPS樹脂は、一般式
一〇一・ー
で表わされる繰り返し単位からなる重合体であって、た
と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などのアξド
系溶媒もしくはスルホランなど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
の熔融粘度が約20〜100ポアズぐらいの低粘度低分
子量のPPS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、或いは意図的に
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.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ため、転勤体4をポケッ
ト部3へ組み込む際に柔軟性を必要とする保持器の素材
としては不適当であった.
一方、直鎖状PPS樹脂は重合段階で直鎖状に分子鎖を
高分子量にまで戒長させた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
という特徴があり、この直鎖状pps樹脂を転がり軸受
用保持器として使用する提案が特開昭64−79419
に開示されている.しかし、この直鎖状PPSI脂から
なる軸受用保持器は、確かに組み立て時の組み込み性に
は優れているのだが、熱安定性や高温(150℃以上)
での耐クリープ特性などの機械的特性などが劣っており
、軸受用の保持器として使用した場合には、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、軸受けの性能を低下さ
せるものであった.
〔発明が解決しようとする課題〕
この発明は、上記の直鎖状pps樹脂または架橋性PP
S樹脂からなる保持器が有する問題を解決し、所要の柔
軟性を有して転勤体を組み込みやすく機械的強度ととも
に耐薬品性をも兼ね備え、しがち高温における変形率の
低い保持器を提供することを技術的課題としている.
rim題を解決するための手段〕
上記の課題を解決するため、第1の発明においては、重
合上りの溶融粘度が350〜3000ポアズのpps樹
脂を架橋して得られる架橋性PPS樹脂と繊維状強化材
とからなる組成物によって保持器を形成し、第2の発明
では第lの発明の架橋性pps樹脂と繊維状強化材及び
フッ素樹脂とからなるma物を素材として転がり軸受用
保持器を形成したのである.
(作用〕
この発明の保持器の素材となる重合上りの熔融粘度が3
50〜3000ポアズのPPS樹脂を架橋して得られた
架橋性PPS樹脂は、柔軟性を有するとともに高温での
機械的特性に優れている.従って、このような架橋性P
PS樹脂と繊維状強化材の二成分およびフッ素樹脂の三
成分がらなるXJl或物で形威された保持器は、適度な
柔軟性を有して組立時に破損することがなく、また組み
込み性に優れ、使用時における高温での変形率が低いも
のとなる.この発明における架橋性PPS樹脂は、重合
上りの溶融粘度が350〜3000ポアズであり、望ま
しくは500〜1000ポアズのものである.なぜなら
ば、重合上りの溶融粘度が350ポアズより小さいPP
S樹脂を架橋させた架橋性pps樹脂は、機械的強度と
ともに柔軟性に欠け、このような架橋性のPPS樹脂を
保持器として使用すると、転勤体を組み込む時に破損し
やすいからである.また、3000ポアズより大きい場
合には、高温での耐クリープ性に劣り、軸受用の保持器
として使用した場合、保持器が変形してしまう.
重合上りのPPS摺脂を架橋するには、前記した架橋方
法と同様に、空気中における融点以下での加熱または架
橋剤、分岐剤を添加することによって行なう。このよう
にして生成した架橋性PPS樹脂の78融粘度は、10
00〜40000ポアズであり、望ましくはl400〜
20000ポアズであればよく、さらに望ましくはl5
00〜10000ポアズであれば一層よい。その場合、
溶融粘度が1400ポアズより小さい架橋性PPS樹脂
は、150゜C以上の高温域で耐クリープ特性などの機
械的特性が低下し、変形しやすいので好ましくない.
20000ポアズより大きい架橋性pps樹脂は、架橋
前の溶融粘度が350〜3000ポアズであっても、戒
形性が劣り、また柔軟性が低下して、保持器に転勤体を
組み込み難く、好ましくない.なお、前記の溶融粘度の
測定条件は、下記のとおりである.
測定温度 =300゜C、
オリフィス 二 穴径1mm、長さ10m測定荷重
: 20kg/ai、
測 定 機 : 高化式フローテスタ予熱時間: 6
分
また、架橋性pps樹脂の熱安定性は、上記の溶融粘度
測定条件にて、予熱6分後と30分後の熔融粘度の変化
率が−50〜150%の範囲であることが好ましい.な
お、変化率は下記の式で表わされるものである.
P,。−P6
変化率 − XIOO
P,
以上のような条件を満足する架橋性PPS樹脂としてた
とえば、トーブレン社製: T − 4 (2)、Tウ
007などが挙げられる。As is well known, plastic rolling bearing cages (
As for cages (hereinafter referred to as cages), so-called nylon cages made of polyamide resin are widely used, which have excellent mechanical properties such as moldability and flexibility, and productivity such as raw material cost. As shown in FIG. 1, such a cage 1 has a claw portion 2 at the top and a pocket portion 3 with a narrow entrance and exit, and a transfer body 4 such as a steel ball is incorporated therein so as to be freely rotatable. It is something to keep. However, this nylon retainer 1 is susceptible to nylon under continuous use at temperatures above 120"C, or under conditions in which it comes into contact with oils or other acidic agents to which extreme pressure additives or other additives have been added. Polyphenylene sulfide resin (hereinafter referred to as polyphenylene sulfide resin) is an alternative material to nylon, which is used under high temperature conditions and is relatively inexpensive. , abbreviated as pps resin),
It has excellent heat resistance, chemical resistance, and formability.
This PPS resin is a polymer consisting of repeating units represented by the general formula 101.
It is obtained by reacting in an ξ-do solvent such as methylpyrrolidone or dimethylacetamide or a sulfone solvent such as sulfolane, and the PPS resin at this stage is considered as the polymerized product. Furthermore, there are two types of PPS resins: crosslinkable pps resins (also called branched PPS resins) and linear pps resins. The former crosslinkable pps resin is produced by heating a low-viscosity, low-molecular-weight PPS resin with a melt viscosity of about 20 to 100 poise in air to below its melting point to cause oxidation crosslinking to increase the melt viscosity. Alternatively, a crosslinked or branched structure is introduced by intentionally adding a crosslinking agent or a branching agent to increase the melt viscosity. However, although the crosslinkable PPS resin obtained in this way has an increased melt viscosity, that is, improved heat resistance, it is considerably brittle and lacks flexibility. It was unsuitable as a material for a cage that requires flexibility when incorporated into a cage. On the other hand, linear PPS resin is a PPS resin whose molecular chains have been lengthened to a high molecular weight in a straight chain during the polymerization stage, and is characterized by being extremely flexible and tough compared to the above-mentioned crosslinkable PPS resin. The use of this linear pps resin as a cage for rolling bearings was proposed in JP-A-64-79419.
It is disclosed in However, although bearing cages made of this linear PPSI fat are certainly easy to assemble during assembly, they have poor thermal stability and high temperature (over 150°C)
It has poor mechanical properties such as creep resistance, and when used as a cage for bearings, the cage deforms due to centrifugal force and comes into contact with the outer ring, generating abnormal frictional heat. , which deteriorated the lubricant and reduced the performance of the bearing. [Problems to be Solved by the Invention] This invention solves the above-mentioned linear pps resin or crosslinkable PP resin.
To solve the problems of cages made of S resin, to provide a cage that has the necessary flexibility, makes it easy to incorporate transfer bodies, has mechanical strength and chemical resistance, and has a low deformation rate at high temperatures. This is considered a technical issue. Means for Solving the rim Problem] In order to solve the above problem, in the first invention, a crosslinkable PPS resin obtained by crosslinking a pps resin having a melt viscosity of 350 to 3000 poise after polymerization and a fibrous A cage is formed from a composition consisting of a reinforcing material, and in a second invention, a cage for a rolling bearing is made of a ma material made of a crosslinkable pps resin of the first invention, a fibrous reinforcing material, and a fluororesin. It was formed. (Function) The melt viscosity after polymerization, which is the material for the cage of this invention, is 3.
Crosslinkable PPS resins obtained by crosslinking PPS resins of 50 to 3000 poise are flexible and have excellent mechanical properties at high temperatures. Therefore, such crosslinkable P
The cage made of XJL, which is composed of two components of PS resin, fibrous reinforcement material, and three components of fluororesin, has appropriate flexibility, does not break during assembly, and is easy to assemble. Excellent, with low deformation rate at high temperatures during use. The crosslinkable PPS resin in this invention has a melt viscosity of 350 to 3000 poise after polymerization, preferably 500 to 1000 poise. This is because PP has a melt viscosity of less than 350 poise after polymerization.
This is because a cross-linked PPS resin made by cross-linking S resin lacks mechanical strength and flexibility, and if such a cross-linked PPS resin is used as a cage, it is likely to be damaged when a transfer body is installed. Moreover, if it is larger than 3000 poise, the creep resistance at high temperatures is poor, and when used as a cage for a bearing, the cage will be deformed. Crosslinking of the PPS resin after polymerization is carried out by heating it in air below its melting point or by adding a crosslinking agent or a branching agent, as in the above-mentioned crosslinking method. The crosslinkable PPS resin thus produced has a melt viscosity of 78
00 to 40,000 poise, preferably l400 to
It may be 20,000 poise, more preferably l5
00 to 10,000 poise is even better. In that case,
Crosslinkable PPS resins with a melt viscosity of less than 1400 poise are undesirable because their mechanical properties such as creep resistance deteriorate at high temperatures of 150°C or higher, and they tend to deform.
A crosslinkable pps resin larger than 20,000 poise is undesirable because even if the melt viscosity before crosslinking is 350 to 3,000 poise, the shapeability is poor and the flexibility is reduced, making it difficult to incorporate the transfer body into the cage. .. The conditions for measuring the melt viscosity described above are as follows. Measurement temperature = 300°C, orifice 2 hole diameter 1mm, length 10m measurement load
: 20kg/ai, Measuring device: Koka type flow tester Preheating time: 6
Furthermore, regarding the thermal stability of the crosslinkable pps resin, it is preferable that the rate of change in melt viscosity after 6 minutes and 30 minutes of preheating is in the range of -50 to 150% under the above melt viscosity measurement conditions. The rate of change is expressed by the following formula. P. -P6 Rate of Change -XIOO P, Examples of crosslinkable PPS resins that satisfy the above conditions include T-4 (2) and T-007 manufactured by Toblen.
つぎに、この発明において含まれる繊維状強化材とはP
PS樹脂を溶融威形する際の温度に耐えるものであれば
特に限定されるものではなく、繊維状強化材としては、
ガラス繊維、炭素繊維、グラファイト繊維、ウオラスト
ナイト、シリコンカーバイトホイスカー、サファイアホ
イスカー、鋼線、銅線、ステンレス線などの耐熱性無機
単一繊維、タングステン芯線または炭素繊維などにボロ
ンもしくは炭化ケイ素繊維などを蒸着したいわゆるボロ
ン繊維もしくは炭化ケイ素繊維などの耐熱無機複合繊維
、芳香族ボリア嵩ド繊維などの耐熱有機繊維などを例示
することが出来る。なお、上記の繊維状強化材としては
、コスト面、人手の容易性、取扱いの簡便性などから、
ガラス繊維が特に好ましいといえる。Next, the fibrous reinforcing material included in this invention is P
There is no particular limitation as long as it can withstand the temperature when PS resin is melted and shaped, and the fibrous reinforcing material may include:
Glass fiber, carbon fiber, graphite fiber, wollastonite, silicon carbide whisker, sapphire whisker, heat-resistant inorganic single fiber such as steel wire, copper wire, stainless steel wire, boron or silicon carbide fiber with tungsten core wire or carbon fiber, etc. Examples thereof include heat-resistant inorganic composite fibers such as boron fibers or silicon carbide fibers, and heat-resistant organic fibers such as aromatic boria bulk fibers. In addition, the above-mentioned fibrous reinforcing materials include:
Glass fiber is particularly preferred.
このガラス繊維としては、SiOz、B20,、AIt
Oz、CaO 、NatO、K.Oなどを戒分とする無
機ガラスから得られ、一般に無アルカリガラス(Eガラ
スと略記)、含アルカリガラス(Cガラス、Aガラスと
略記)などがあるが、この発明においてはEガラスで織
維長0.1〜10圓のものが好ましく、またその線径は
15μ鵬以下特に10fm以下のものが好ましい。なぜ
なら繊維径が1sttmよりも大きいガラス繊維を用い
ると、威形して得られる転がり軸受用プラスチック保持
器材は柔軟性に欠け、組み立て時の組み込み性が悪くな
るからである。なお、PPS樹脂との親和性をもたせる
ために、繊維状強化材はア〔ノシラン、エボキシシラン
、メルカプトシラン等のシランカップリング剤やクロム
系カップリング剤を含むサイジング剤さらには集束を目
的とした集束剤などによって処理されたものであっても
良い。As this glass fiber, SiOz, B20, AIt
Oz, CaO, NatO, K. It is obtained from inorganic glass containing O, etc., and generally includes alkali-free glass (abbreviated as E glass) and alkali-containing glass (abbreviated as C glass and A glass). Preferably, the length is from 0.1 to 10 mm, and the wire diameter is preferably 15 μm or less, particularly 10 fm or less. This is because, if glass fibers with a fiber diameter larger than 1 sttm are used, the resulting plastic retainer for rolling bearings will lack flexibility and will be difficult to assemble during assembly. In addition, in order to have affinity with the PPS resin, the fibrous reinforcing material is used as a sizing agent containing a silane coupling agent such as anosilane, epoxysilane, or mercaptosilane, a chromium-based coupling agent, and a sizing agent for the purpose of focusing. It may also be one that has been treated with a chemical or the like.
本発明におけるフッ素樹脂としては、例えば四フノ化エ
チレン樹脂(PTFEと略称する)、テトラフルオロエ
チレンーバーフルオロアルキルビニルエーテル共重合体
(PFAと略称する)、テトラフルオロエチレンーへキ
サフルオ口プロピレン共重合体、エチレンーテトラフル
オ口エチレン共重合体、テトラフルオ口チレンーフルオ
ロアルキルビニルエーテルーフルオロオレフィン共重合
体、ポリトリク口口フルオ口エチレンおよびボリフッ化
ビニリデン等が挙げられる。Examples of the fluororesin in the present invention include tetrafluoroethylene resin (abbreviated as PTFE), tetrafluoroethylene-perfluoroalkyl vinyl ether copolymer (abbreviated as PFA), and tetrafluoroethylene-hexafluoropropylene copolymer. , ethylene-tetrafluoroethylene copolymer, tetrafluoroethylene-fluoroalkyl vinyl ether-fluoroolefin copolymer, polytricfluoroethylene, polyvinylidene fluoride, and the like.
本発明における各威分の含有比率(重量%)は次のとお
りである。The content ratio (weight %) of each component in the present invention is as follows.
架橋性pps樹脂(A)
繊維状強化材 (B)
フン素樹脂(C)
■ A:B=30〜98 : 70〜2、好ましくは5
0〜95:50〜5、
■ A:B:C=45〜8g : 10〜40:2〜1
5、好ましくは65〜85:12〜35:2〜10、フ
ノ素樹脂の添加量が2%以下では柔軟性に欠け、15%
以上になると高温での機枝的強度が劣るので好ましくな
い。Crosslinkable pps resin (A) Fibrous reinforcing material (B) Fluorine resin (C) ■ A:B=30-98: 70-2, preferably 5
0~95:50~5, ■ A:B:C=45~8g: 10~40:2~1
5. Preferably 65-85:12-35:2-10, if the amount of fluororesin added is less than 2%, flexibility will be lacking, and 15%
If it exceeds this level, the mechanical strength at high temperatures will deteriorate, which is not preferable.
また、この発明の効果を損なわない限り各種の充填材を
添加することともできる.このような充填材として、芳
香族ポリエーテルケトン樹脂、ポリエーテルイごド樹脂
、ポリエーテルサルフォン樹脂、ボリアくドイミド樹脂
、耐熱性ポリアミド樹脂、フェノール系樹脂、芳香族ポ
リエステル樹脂、ポリイミド樹脂、フッ素樹脂、シリコ
ーン樹脂の有機質耐熱性高分子材料を始めとし、グラフ
ァイトまたは亜鉛、アルミニウム、マグネシウムなどの
金属もしくは酸化物などの熱伝導改良用無機粉末、ガラ
スビーズ、シリカバルーン、珪藻土、石綿、炭酸マグネ
シウム、炭酸カルシウム、酸化カルシウム、フッ化カル
シウム、水酸化カルシウム等の無機質粉末、二硫化モリ
ブデン、グラファイト、カーボン、マイ力、タルク、三
酸化モリブデン等の潤滑性向上用無機質粉末、および酸
化鉄、硫化カドξウム、セレン化カドミウム、カーポン
ブラック等の無機質顔料、シリコーンオイル、エステル
オイル、フッ素オイル、ポリフェニレンエーテルオイル
、ワックス、ステアリン酸亜鉛などの内部滑剤的添加剤
など数多くのものを例示することができる.
以上述べたpps樹脂、繊維状強化材、フッ素樹脂およ
びその他添加剤等の混合方法は、特に限定されるもので
はなく、ヘンシェルミキサー、ボール旦ル、タンブラー
旦キサー等の混合機を用いて乾式混合した後に、熱ロー
ル、ニーダ、バンバリーミキサー、溶融押出機などで溶
融混合して成形材料としてたとえばペレット状にし、こ
れを射出威形機などによって転がり軸受用保持器として
所定の形状に溶融成形すればよい.成形条件は特に限定
されることなく、PPS樹脂の通常の戒形条件で充分で
ある.
この発明の実施例および比較例に使用した原材料を一括
して示す。なお、PPS樹脂については、重合上りの熔
融粘度:P,、架橋後の溶融粘度:P2(6分後).P
x (30分後)についても併記する。Furthermore, various fillers may be added as long as they do not impair the effects of this invention. Such fillers include aromatic polyetherketone resin, polyether oxide resin, polyether sulfone resin, boria-dimide resin, heat-resistant polyamide resin, phenolic resin, aromatic polyester resin, polyimide resin, fluororesin, Organic heat-resistant polymer materials such as silicone resins, inorganic powders for improving thermal conductivity such as graphite or metals or oxides such as zinc, aluminum, and magnesium, glass beads, silica balloons, diatomaceous earth, asbestos, magnesium carbonate, and calcium carbonate. , inorganic powders such as calcium oxide, calcium fluoride, and calcium hydroxide, inorganic powders for improving lubricity such as molybdenum disulfide, graphite, carbon, miryoku, talc, and molybdenum trioxide, and iron oxide, cadmium sulfide, Examples include inorganic pigments such as cadmium selenide and carbon black, silicone oils, ester oils, fluorine oils, polyphenylene ether oils, waxes, and internal lubricant additives such as zinc stearate. The method of mixing the pps resin, fibrous reinforcing material, fluororesin, and other additives described above is not particularly limited, and dry mixing is performed using a mixer such as a Henschel mixer, a ball tanker, or a tumbler mixer. After that, it is melt-mixed using a heated roll, kneader, Banbury mixer, melt extruder, etc. to form a molding material, such as pellets, and then melt-molded into a predetermined shape as a cage for rolling bearings using an injection molding machine, etc. good. The molding conditions are not particularly limited, and normal molding conditions for PPS resin are sufficient. The raw materials used in Examples and Comparative Examples of this invention are collectively shown below. Regarding PPS resin, melt viscosity after polymerization: P, melt viscosity after crosslinking: P2 (after 6 minutes). P
x (30 minutes later) is also written.
■架橋性pps樹脂(トープレン社製FT−4(2)、
P + = 700ポアズ、Pt =1840ポアズ、
P3−1350ポアズ)
■架橋性PPS樹脂(トープレン社製:TX−001、
P, = 700ポアズ、P z =1030ポアズ、
P,= 13400ポアズ)
■架橋性pps樹脂(トーブレン社製:試作品PPS(
1)、P + = 700ポアズ、Pg””1880ポ
アズ、P,−1530ポアズ)
■架橋性PPS樹脂(トープレン社製:試作品P P
S (2)、P,=700ポアズ、P. =2320ポ
アズ、P,−2150ポアズ)
■架橋性PPS樹脂(トープレン社製:T−4(1)、
PI−300ポアズ、P. =2450ポアズ、P3=
3520ポアズ)
■直鎖状PPS樹脂(呉羽化学工業社製:KPS#21
4 、溶融粘度−1400ポアズ)■ガラス繊維(旭ガ
ラスファイバーグラス社製: CSO30E404、繊
維系6μ一■ガラス繊維(旭ガラスファイハーグラス社
製: CSO30EF丁562、繊維系6pm)■フッ
素樹脂PTFE(喜多村社製: KTL−610)[相
]フッ素樹脂PFA(三井デュポンフロロケミカル社製
:肝−10)
以上の原材料を第1表及び第2表に示したような割合で
ヘンシェルξキサーを用いて乾式混合して、二軸溶融押
出機に供給し、シリンダー温度270〜330′Cスク
リュー回転数50−100rpmの条件にて溶融滌合お
よび造粒をした。その後シリンダー温度280〜340
’C、金型温度100〜150’C、射出圧力500〜
1000kg/cJの条件にて第1図に示したような軸
受5203の保持器1を射出成形し、次に示した試験を
行なった。■Crosslinkable pps resin (FT-4 (2) manufactured by Toprene Co., Ltd.,
P + = 700 poise, Pt = 1840 poise,
P3-1350 poise) ■Crosslinkable PPS resin (Toprene: TX-001,
P, = 700 poise, P z = 1030 poise,
P, = 13400 poise) ■Crosslinkable pps resin (manufactured by Torbren: prototype PPS (
1), P + = 700 poise, Pg""1880 poise, P, -1530 poise) ■Crosslinkable PPS resin (manufactured by Toprene: Prototype P P
S (2), P, = 700 Poise, P. =2320 poise, P, -2150 poise) ■Crosslinkable PPS resin (Toprene: T-4 (1),
PI-300 Poise, P. =2450 poise, P3=
3520 poise) ■Linear PPS resin (manufactured by Kureha Chemical Industry Co., Ltd.: KPS#21
4. Melt viscosity - 1400 poise) ■Glass fiber (manufactured by Asahi Glass Fiber Glass Co., Ltd.: CSO30E404, fiber-based 6μ) ■Glass fiber (manufactured by Asahi Glass Fiber Glass Co., Ltd.: CSO30EF-562, fiber-based 6pm) ■Fluororesin PTFE ( Kitamura Co., Ltd.: KTL-610) [Phase] Fluororesin PFA (Mitsui DuPont Fluorochemical Co., Ltd.: Liver-10) The above raw materials were mixed using Henschel ξ Kisser in the proportions shown in Tables 1 and 2. The mixture was dry-mixed and supplied to a twin-screw melt extruder, where it was melt-blended and granulated at a cylinder temperature of 270-330'C and a screw rotation speed of 50-100 rpm.Then, the cylinder temperature was 280-340'C.
'C, mold temperature 100~150'C, injection pressure 500~
The cage 1 of the bearing 5203 as shown in FIG. 1 was injection molded under the condition of 1000 kg/cJ, and the following test was conducted.
<1) &Il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の部分の転勤体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、第1、2表に示した.
■保持器の爪の部分の損傷度合:
○・・・・・・全く損傷しない
Δ・・・・・・少し損傷する
×・・・・・・かなり損傷する
■綱球の組み込み性:
O・・・・・・組み込み時に無理なく組み込めるΔ・・
・・・・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第 1 表
注 ※ 保持器外周に擦り傷あり
(2)保持器の爪部の耐久試験
笛3図に示すように、保持器1のポケット部3に球部6
の逢が直径7.16閣である銅1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t具するまでの出し入れ回数を71)
1定し、その値を第1表に示した。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の転勤体4を組み込む際の安全率は
高いといえる。<1) Integration test during assembly As shown in Figure 2, it was actually assembled into the bearing body 5 using a mini-press and the degree of damage caused by the rolling elements 4 (steel balls) to the claw portion 2 of the cage 1 was measured. The assemblability of the steel balls was investigated and judged according to the criteria shown below, and the results are shown in Tables 1 and 2. ■Degree of damage to the claws of the retainer: ○...No damage at all Δ...Slight damage ×...Significant damage ■Easy to install the rope ball: O・・・・・・・Δ that can be easily installed during installation.
...There is a little resistance when assembling × ...There is considerable resistance when assembling Table 1 Note * There are scratches on the outer periphery of the cage (2) Durability test whistle of the cage claws Shown in Figure 3 As shown in FIG.
A rod 7 equipped with a copper ball with a diameter of 7.16 mm is inserted and withdrawn using a testing machine 8 at a speed of 50 times/min until the claw portion 2 of the retainer 1 breaks. 71 times)
1, and the values are shown in Table 1. It can be said that the greater the number of times of loading and unloading, the greater the fatigue strength of the claw portions 2 of the cage 1, and the higher the safety factor when incorporating the transfer body 4 of the cage 1 in the manufacturing process.
(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、フン素ゴムにてシールをした軸受6
203を運転試験機にて、回転数1500Orpmスラ
スト荷重6.8kgf , /M度180゜C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第
1表に示した。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) Cage deformation rate measurement test lubricant (manufactured by Nippon Oil Co., Ltd.: urea-based grease, U295)
Bearing 6 sealed with fluorine rubber and sealed with 0.8g of
203 was operated for 200 hours using an operating test machine under the conditions of rotation speed 1500 rpm, thrust load 6.8 kgf, /M degree 180°C, and the dimensional deformation rate of the cage outer diameter was measured and shown in Table 1. The smaller the dimensional deformation rate is, the less the cage is deformed.
(4)潤滑剤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,○・・・・・
・変色有り、劣化なし
Δ・・・・・・変色有り、少し劣化あり×・・・・・・
変色有り、かなり劣化している第l、第2表からも明ら
かなように、重合上りの78融粘度が、350ポアズ以
上の架橋性PPS樹脂および繊維状強化材からなる保持
器(第l表及び第2表の実施例1〜5)は、重合上りの
熔融粘度が、350ポアズより小さい架橋性pps樹脂
(第1表の比較例lおよび3)および、直饋状のPPS
樹脂(第l表の比較例2および4)に比較して、組み立
て時の組み込み性や保持器の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
剤を劣化させることがない。(4) Lubricant deterioration degree determination test Lubricant after 200 hours of continuous operation under exactly the same conditions as test (3) (Nippon Oil Co., Ltd.: Urea-based grease, U295)
The degree of deterioration was determined and is also listed in Table 1, ○...
・Discoloration, no deterioration Δ・・・Discoloration, slight deterioration×・・・・・・
As is clear from Tables 1 and 2, which show discoloration and considerable deterioration, the cage made of crosslinkable PPS resin and fibrous reinforcing material has a melt viscosity of 78 poise or more after polymerization (Table 1). and Examples 1 to 5 in Table 2) are crosslinkable pps resins whose melt viscosity after polymerization is smaller than 350 poise (Comparative Examples 1 and 3 in Table 1) and straight PPS resins.
Compared to resin (Comparative Examples 2 and 4 in Table 1), it has excellent ease of assembly during assembly and durability of the claws of the cage, and has a low deformation rate in bearings operated at high temperatures. Does not deteriorate lubricant.
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pps樹脂本来の耐熱性、耐薬品性をも兼ね備えた
ものであって、その利用分野はきわめて広く、自動車関
連業界、−i機器関連業界、N.機電子関連業界その他
多くの分野で用いられる転がり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 is flexible and easy to incorporate into the bearing, and even when used at high temperatures, the deformation rate is low, so the bearing will not be damaged. It has the heat resistance and chemical resistance inherent to pps resin, and its application fields are extremely wide, including the automobile-related industry, the i-device-related industry, and the N.P.S. It is ideal as a cage for rolling bearings used in the mechanical/electronic industry 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・・・・・・ポケン
ト部、4・・・・・・転動体、 5・・・・・・
軸受本体。FIG. 1 is a perspective view illustrating the main parts of a cage for rolling bearings;
Figure 2 is a cross-sectional view showing the relationship between a rolling bearing cage and a bearing to examine the ease of incorporating steel balls, and Figure 3 is a plan view of a testing machine illustrating the durability test of the claws of a rolling bearing cage. It is a diagram. DESCRIPTION OF SYMBOLS 1... Rolling bearing cage, 2... Claw portion, 3... Pocket portion, 4... Rolling element, 5......
Bearing body.
Claims (3)
ポリフェニレンサルファイド樹脂を架橋して得られる架
橋性ポリフェニレンサルファイド樹脂と繊維状強化材と
からなる組成物を素材とする転がり軸受用保持器。(1) A cage for a rolling bearing made of a composition comprising a crosslinkable polyphenylene sulfide resin obtained by crosslinking a polyphenylene sulfide resin having a melt viscosity of 350 to 3000 poise after polymerization and a fibrous reinforcing material.
ポリフェニレンサルファイド樹脂を架橋して得られる架
橋性ポリフェニレンサルファイド樹脂と繊維状強化材お
よびフッ素樹脂とからなる組成物を素材とする転がり軸
受用保持器。(2) A cage for rolling bearings made of a composition consisting of a crosslinkable polyphenylene sulfide resin obtained by crosslinking a polyphenylene sulfide resin having a melt viscosity of 350 to 3,000 poise after polymerization, a fibrous reinforcing material, and a fluororesin. .
の溶融粘度が1400〜20000ポアズである請求項
(1)または(2)に記載の転がり軸受用保持器。(3) The cage for a rolling bearing according to claim (1) or (2), wherein the crosslinkable polyphenylene sulfide resin has a melt viscosity of 1,400 to 20,000 poise after crosslinking.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE4041068A DE4041068C2 (en) | 1990-06-25 | 1990-12-20 | Rolling cage |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1-170024 | 1989-06-30 | ||
JP17002489 | 1989-06-30 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0396716A true JPH0396716A (en) | 1991-04-22 |
JP2948626B2 JP2948626B2 (en) | 1999-09-13 |
Family
ID=15897187
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP16624390A Expired - Lifetime JP2948626B2 (en) | 1989-06-30 | 1990-06-25 | Race for roller bearing |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2948626B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2269863A (en) * | 1992-08-19 | 1994-02-23 | Nsk Ltd | Ball bearing for turbocharger |
CN112924177A (en) * | 2021-04-02 | 2021-06-08 | 哈尔滨理工大学 | Rolling bearing fault diagnosis method for improved deep Q network |
-
1990
- 1990-06-25 JP JP16624390A patent/JP2948626B2/en not_active Expired - Lifetime
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2269863A (en) * | 1992-08-19 | 1994-02-23 | Nsk Ltd | Ball bearing for turbocharger |
GB2269863B (en) * | 1992-08-19 | 1996-03-06 | Nsk Ltd | Ball bearing for turbocharger |
US5522667A (en) * | 1992-08-19 | 1996-06-04 | Nsk Ltd. | Ball bearing for turbocharger |
CN112924177A (en) * | 2021-04-02 | 2021-06-08 | 哈尔滨理工大学 | Rolling bearing fault diagnosis method for improved deep Q network |
Also Published As
Publication number | Publication date |
---|---|
JP2948626B2 (en) | 1999-09-13 |
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