JPH10196719A - Damper pulley - Google Patents
Damper pulleyInfo
- Publication number
- JPH10196719A JPH10196719A JP9002376A JP237697A JPH10196719A JP H10196719 A JPH10196719 A JP H10196719A JP 9002376 A JP9002376 A JP 9002376A JP 237697 A JP237697 A JP 237697A JP H10196719 A JPH10196719 A JP H10196719A
- Authority
- JP
- Japan
- Prior art keywords
- eor
- olefin
- ethylene
- molecular weight
- pulley
- 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.)
- Pending
Links
- 229920000642 polymer Polymers 0.000 claims abstract description 36
- 239000000956 alloy Substances 0.000 claims abstract description 32
- 229910045601 alloy Inorganic materials 0.000 claims abstract description 32
- 150000001875 compounds Chemical class 0.000 claims abstract description 21
- 239000004636 vulcanized rubber Substances 0.000 claims abstract description 17
- 238000009826 distribution Methods 0.000 claims abstract description 12
- 150000001993 dienes Chemical class 0.000 claims abstract description 11
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229910052740 iodine Inorganic materials 0.000 claims abstract description 10
- 239000011630 iodine Substances 0.000 claims abstract description 10
- 150000002978 peroxides Chemical class 0.000 claims abstract description 9
- 229920001971 elastomer Polymers 0.000 claims description 42
- 239000004711 α-olefin Substances 0.000 claims description 36
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 35
- 239000005977 Ethylene Substances 0.000 claims description 23
- 229920000089 Cyclic olefin copolymer Polymers 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
- 229920001577 copolymer Polymers 0.000 claims description 6
- OJOWICOBYCXEKR-APPZFPTMSA-N (1S,4R)-5-ethylidenebicyclo[2.2.1]hept-2-ene Chemical group CC=C1C[C@@H]2C[C@@H]1C=C2 OJOWICOBYCXEKR-APPZFPTMSA-N 0.000 claims description 3
- 150000001336 alkenes Chemical class 0.000 claims description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 2
- 239000007788 liquid Substances 0.000 abstract description 18
- 239000000463 material Substances 0.000 abstract description 8
- 238000000034 method Methods 0.000 abstract description 5
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 abstract description 4
- 229920000181 Ethylene propylene rubber Polymers 0.000 abstract description 3
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 abstract description 2
- 229920002943 EPDM rubber Polymers 0.000 abstract 2
- OJOWICOBYCXEKR-UHFFFAOYSA-N 5-ethylidenebicyclo[2.2.1]hept-2-ene Chemical group C1C2C(=CC)CC1C=C2 OJOWICOBYCXEKR-UHFFFAOYSA-N 0.000 abstract 1
- 239000006229 carbon black Substances 0.000 description 12
- 238000012360 testing method Methods 0.000 description 12
- 238000013016 damping Methods 0.000 description 11
- 239000000203 mixture Substances 0.000 description 10
- 238000004073 vulcanization Methods 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 7
- 229910052717 sulfur Inorganic materials 0.000 description 7
- 239000011593 sulfur Substances 0.000 description 7
- -1 ethylene-ethylene Chemical group 0.000 description 6
- 239000003921 oil Substances 0.000 description 4
- 235000019198 oils Nutrition 0.000 description 4
- 239000003208 petroleum Substances 0.000 description 4
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- 239000004902 Softening Agent Substances 0.000 description 3
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 238000013329 compounding Methods 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 238000004898 kneading Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 239000012188 paraffin wax Substances 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- 235000014692 zinc oxide Nutrition 0.000 description 3
- 239000011787 zinc oxide Substances 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- DCTOHCCUXLBQMS-UHFFFAOYSA-N 1-undecene Chemical compound CCCCCCCCCC=C DCTOHCCUXLBQMS-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 230000002902 bimodal effect Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- 239000011280 coal tar Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000010734 process oil Substances 0.000 description 2
- 229920005604 random copolymer Polymers 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 238000009864 tensile test Methods 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- MYOQALXKVOJACM-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy pentaneperoxoate Chemical compound CCCCC(=O)OOOC(C)(C)C MYOQALXKVOJACM-UHFFFAOYSA-N 0.000 description 1
- NALFRYPTRXKZPN-UHFFFAOYSA-N 1,1-bis(tert-butylperoxy)-3,3,5-trimethylcyclohexane Chemical compound CC1CC(C)(C)CC(OOC(C)(C)C)(OOC(C)(C)C)C1 NALFRYPTRXKZPN-UHFFFAOYSA-N 0.000 description 1
- HSLFISVKRDQEBY-UHFFFAOYSA-N 1,1-bis(tert-butylperoxy)cyclohexane Chemical compound CC(C)(C)OOC1(OOC(C)(C)C)CCCCC1 HSLFISVKRDQEBY-UHFFFAOYSA-N 0.000 description 1
- UBRWPVTUQDJKCC-UHFFFAOYSA-N 1,3-bis(2-tert-butylperoxypropan-2-yl)benzene Chemical compound CC(C)(C)OOC(C)(C)C1=CC=CC(C(C)(C)OOC(C)(C)C)=C1 UBRWPVTUQDJKCC-UHFFFAOYSA-N 0.000 description 1
- VQOXUMQBYILCKR-UHFFFAOYSA-N 1-Tridecene Chemical compound CCCCCCCCCCCC=C VQOXUMQBYILCKR-UHFFFAOYSA-N 0.000 description 1
- KPAPHODVWOVUJL-UHFFFAOYSA-N 1-benzofuran;1h-indene Chemical compound C1=CC=C2CC=CC2=C1.C1=CC=C2OC=CC2=C1 KPAPHODVWOVUJL-UHFFFAOYSA-N 0.000 description 1
- VYNQWGXTLZDYFX-UHFFFAOYSA-N 1-benzoylperoxyhexyl benzenecarboperoxoate Chemical compound C=1C=CC=CC=1C(=O)OOC(CCCCC)OOC(=O)C1=CC=CC=C1 VYNQWGXTLZDYFX-UHFFFAOYSA-N 0.000 description 1
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 1
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1-dodecene Chemical compound CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 1
- GQEZCXVZFLOKMC-UHFFFAOYSA-N 1-hexadecene Chemical compound CCCCCCCCCCCCCCC=C GQEZCXVZFLOKMC-UHFFFAOYSA-N 0.000 description 1
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 1
- HFDVRLIODXPAHB-UHFFFAOYSA-N 1-tetradecene Chemical compound CCCCCCCCCCCCC=C HFDVRLIODXPAHB-UHFFFAOYSA-N 0.000 description 1
- YKTNISGZEGZHIS-UHFFFAOYSA-N 2-$l^{1}-oxidanyloxy-2-methylpropane Chemical group CC(C)(C)O[O] YKTNISGZEGZHIS-UHFFFAOYSA-N 0.000 description 1
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 239000004594 Masterbatch (MB) Substances 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- 239000004264 Petrolatum Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- LFYJSSARVMHQJB-QIXNEVBVSA-N bakuchiol Chemical compound CC(C)=CCC[C@@](C)(C=C)\C=C\C1=CC=C(O)C=C1 LFYJSSARVMHQJB-QIXNEVBVSA-N 0.000 description 1
- AGXUVMPSUKZYDT-UHFFFAOYSA-L barium(2+);octadecanoate Chemical compound [Ba+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O AGXUVMPSUKZYDT-UHFFFAOYSA-L 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 238000003763 carbonization Methods 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000011294 coal tar pitch Substances 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000010685 fatty oil Substances 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 238000010068 moulding (rubber) Methods 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- CCCMONHAUSKTEQ-UHFFFAOYSA-N octadec-1-ene Chemical compound CCCCCCCCCCCCCCCCC=C CCCMONHAUSKTEQ-UHFFFAOYSA-N 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- PJLHTVIBELQURV-UHFFFAOYSA-N pentadecene Natural products CCCCCCCCCCCCCC=C PJLHTVIBELQURV-UHFFFAOYSA-N 0.000 description 1
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 1
- 238000010060 peroxide vulcanization Methods 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000002040 relaxant effect Effects 0.000 description 1
- 229960003656 ricinoleic acid Drugs 0.000 description 1
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000010059 sulfur vulcanization Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 229940098697 zinc laurate Drugs 0.000 description 1
- GPYYEEJOMCKTPR-UHFFFAOYSA-L zinc;dodecanoate Chemical compound [Zn+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O GPYYEEJOMCKTPR-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
- F16F—SPRINGS; SHOCK-ABSORBERS; MEANS FOR DAMPING VIBRATION
- F16F15/00—Suppression of vibrations in systems; Means or arrangements for avoiding or reducing out-of-balance forces, e.g. due to motion
- F16F15/10—Suppression of vibrations in rotating systems by making use of members moving with the system
- F16F15/14—Suppression of vibrations in rotating systems by making use of members moving with the system using masses freely rotating with the system, i.e. uninvolved in transmitting driveline torque, e.g. rotative dynamic dampers
- F16F15/1407—Suppression of vibrations in rotating systems by making use of members moving with the system using masses freely rotating with the system, i.e. uninvolved in transmitting driveline torque, e.g. rotative dynamic dampers the rotation being limited with respect to the driving means
- F16F15/1414—Masses driven by elastic elements
- F16F15/1435—Elastomeric springs, i.e. made of plastic or rubber
- F16F15/1442—Elastomeric springs, i.e. made of plastic or rubber with a single mass
Landscapes
- Engineering & Computer Science (AREA)
- General Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Acoustics & Sound (AREA)
- Aviation & Aerospace Engineering (AREA)
- Mechanical Engineering (AREA)
- Vibration Prevention Devices (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、ダンパマスとプー
リとの間に弾性体が介在されてなるダンパプーリに関す
る。The present invention relates to a damper pulley having an elastic body interposed between a damper mass and a pulley.
【0002】特に、ダンパマス(ハブ)12とプーリ1
4との間に弾性体16を単純圧入するタイプのダンパプ
ーリ18に好適な発明である(図1参照)。弾性体を接
着剤用いたり、リング圧入したりするタイプのダンパプ
ーリにも、本発明は、適用可能である。In particular, a damper mass (hub) 12 and a pulley 1
The present invention is suitable for a damper pulley 18 of a type in which the elastic body 16 is simply press-fitted between the elastic body 16 and the damper pulley 4 (see FIG. 1). The present invention is also applicable to a damper pulley of a type in which an elastic body is used as an adhesive or a ring is press-fitted.
【0003】なお、本明細書の「特許請求の範囲」及び
「発明の詳細な説明」の各欄における下記特性値の各意
味は下記の通りである。[0003] The meanings of the following characteristic values in the columns of "claims" and "detailed description of the invention" in this specification are as follows.
【0004】損失正接(tan δ):後述の動的粘弾性
試験で求めた値。[0004] Loss tangent (tan δ): a value determined by a dynamic viscoelasticity test described later.
【0005】極限粘度[η]:135℃デカリン中で
の測定値。[0005] Intrinsic viscosity [η]: measured at 135 ° C in decalin.
【0006】分子量分布指数(MW /Mn ):後述の
ゲルパーミエーションクロマトグラフィー(GPC法)
測定により求めた分子量分布における重量平均分子量
(M W )を数平均分子量(Mn )で割った指数。The molecular weight distribution index (MW / Mn ): Described later
Gel permeation chromatography (GPC method)
Weight average molecular weight in molecular weight distribution determined by measurement
(M W ) Is the number average molecular weight (Mn Index divided by).
【0007】また、以下の説明で、配合単位は、特に断
らない限り、重量単位である。In the following description, the blending unit is a weight unit unless otherwise specified.
【0008】[0008]
【従来の技術】従来のダンパプーリおける上記弾性体
は、NR/SBR、SBR、塩素化IIR、NBR、水
添NBR等のゴム材料で形成されていた(特開平62−
297557号公報)。2. Description of the Related Art The elastic body of a conventional damper pulley is formed of a rubber material such as NR / SBR, SBR, chlorinated IIR, NBR, hydrogenated NBR, etc.
297557).
【0009】[0009]
【発明が解決しようとする課題】しかし、昨今のエンジ
ンルーム内の温度上昇に伴う耐熱性向上の要求には、こ
れらのゴム材料では、対応し難くなっている。However, it is difficult for these rubber materials to respond to the recent demand for improvement in heat resistance due to a rise in temperature in the engine room.
【0010】そこで、一般に耐熱性に優れたエチレンプ
ロピレンゴム系材料、即ち、エチレン・α−オレフィン
共重合体ゴム(EOR)材料を使用することが考えられ
る。Therefore, it is generally considered to use an ethylene propylene rubber-based material having excellent heat resistance, that is, an ethylene / α-olefin copolymer rubber (EOR) material.
【0011】しかし、汎用のEORの場合、低温柔軟性
に劣る、損失正接(tan δ)が小さいという問題点があ
る。However, a general-purpose EOR has problems that it is inferior in low-temperature flexibility and has a small loss tangent (tan δ).
【0012】そこで、本発明者らは、本願出願人の一人
が先に提案した、特定の三元系EORゴム(エチレン・
α−オレフィン・非共役ジエン共重合体ゴム)と特定の
液状二元系EOR(液状エチレン・α−オレフィン共重
合体ゴム)とからなるポリマーアロイをベースとする硫
黄加硫系の耐熱防振用のゴム組成物(ゴム配合物)(特
開平6−001819号)に着目して、ダンパプーリに
適用できないかを検討した。Therefore, the present inventors have proposed a specific ternary EOR rubber (ethylene-ethylene rubber) previously proposed by one of the present applicants.
For heat and vibration proof of sulfur vulcanization system based on polymer alloy composed of α-olefin / non-conjugated diene copolymer rubber) and specific liquid binary EOR (liquid ethylene / α-olefin copolymer rubber) By paying attention to the rubber composition (rubber compound) (Japanese Patent Application Laid-Open No. 6-001819), it was examined whether or not it can be applied to a damper pulley.
【0013】しかし、当該EORブレンドゴム材料で成
形した弾性体をダンパプーリに適用した場合、熱劣化後
の弾性体の硬度変化量(ΔHS )が大きくて、硬度に依
存する共振周波数変化量が大きくなり、安定したダンパ
プーリ性能が得難いとともに、前述のような単純圧入タ
イプに適用した場合、耐へたり性(熱試験後の圧縮永久
歪み率(CS)が大きい)に問題があり、ダンパマス及
び/またはプーリと弾性体との間の結合性に問題がある
ことが分かった(表1比較例参照)。即ち、ダンパプー
リの要求性能を満足させるには、やはり、耐熱性が必ず
しも十分とは言えなかった。However, when an elastic body molded from the EOR blend rubber material is applied to a damper pulley, the elastic body has a large change in hardness (ΔH S ) after thermal degradation, and a large resonance frequency change depending on the hardness. In addition, it is difficult to obtain stable damper pulley performance, and when applied to the simple press-fitting type as described above, there is a problem in set resistance (high compression set (CS) after a thermal test), and damper mass and / or It was found that there was a problem in the connection between the pulley and the elastic body (see Comparative Example in Table 1). That is, the heat resistance was not always sufficient to satisfy the required performance of the damper pulley.
【0014】本発明は上記にかんがみて、高温雰囲気下
でも安定した防振性能を発揮できるダンパプーリを提供
することを目的とする。In view of the above, an object of the present invention is to provide a damper pulley capable of exhibiting a stable vibration-proof performance even in a high-temperature atmosphere.
【0015】本発明の他の目的は、高温雰囲気下でも、
単純圧入タイプのダンパプーリにおいて、ダンパマス及
び/またはプーリと弾性体との間の結合性に問題が発生
し難いダンパプーリを提供することにある。Another object of the present invention is to provide a high-temperature atmosphere,
An object of the present invention is to provide a damper pulley of a simple press-fit type that does not easily cause a problem in damper mass and / or connectivity between the pulley and the elastic body.
【0016】[0016]
【課題を解決するための手段】本発明者らは、上記課題
を解決するために、鋭意開発に努力をする過程で、前記
耐熱防振用のゴム配合物において、加硫系を特定すると
ともに、液状二元系EORとして極限粘度をシフトさせ
たものでダンパプーリの弾性体を形成すれば上記課題が
解決できることを知見して、下記構成のダンパプーリに
想到した。Means for Solving the Problems In order to solve the above-mentioned problems, the inventors of the present invention have sought to develop a vulcanization system in the rubber compound for heat and vibration proof while working hard on development. The present inventors have found that the above problem can be solved by forming the elastic body of the damper pulley with a liquid binary EOR having a limiting viscosity shifted, and have arrived at a damper pulley having the following configuration.
【0017】ダンパマスとプーリとの間に弾性体が介在
されてなるダンパプーリにおいて、弾性体が、下記要件
(1) 〜(3) を満たすポリマーアロイをベースとする過酸
化物加硫系の加硫物であって、損失正接(tan δ)が
0.20〜0.35であるものから形成されていること
を特徴とする。In the damper pulley in which an elastic body is interposed between the damper mass and the pulley, the elastic body has the following requirements.
A peroxide vulcanized vulcanizate based on a polymer alloy satisfying (1) to (3) and having a loss tangent (tan δ) of 0.20 to 0.35. It is characterized by being.
【0018】(1) ポリマーアロイは、エチレン・α−オ
レフィン・非共役ジエン共重合体ゴム(A):80〜6
0重量%と液状エチレン・α−オレフィン共重合体ゴム
(B):2040重量%からなる。(1) The polymer alloy is an ethylene / α-olefin / non-conjugated diene copolymer rubber (A): 80 to 6
0% by weight and liquid ethylene / α-olefin copolymer rubber (B): 2040% by weight.
【0019】(2) エチレン・α−オレフィン・非共役ジ
エン共重合体ゴムは、エチレンと炭素原子数3〜20の
α−オレフィンと非共役ジエンとからなり、かつ、エチ
レンとα−オレフィンとのモル比が60/40〜73/
27であり、分子量分布指数(MW /Mn )が4未満で
あり、極限粘度[η]が2.7〜5.0dL/gであ
り、ヨウ素価が10〜40であり、非共役ジエンが5−
エチリデン−2−ノルボルネンである。(2) The ethylene / α-olefin / non-conjugated diene copolymer rubber comprises ethylene, an α-olefin having 3 to 20 carbon atoms and a non-conjugated diene, and is composed of ethylene and α-olefin. The molar ratio is 60 / 40-73 /
27, a molecular weight distribution index (M w / M n ) of less than 4, an intrinsic viscosity [η] of 2.7 to 5.0 dL / g, an iodine value of 10 to 40, and a non-conjugated diene. Is 5-
Ethylidene-2-norbornene.
【0020】(3) 液状エチレン・α−オレフィン共重合
体ゴムは、エチレンと炭素原子数3〜20のα−オレフ
ィンとからなり、かつ、エチレンとα−オレフィンとの
モル比が50/50〜78/22であり、極限粘度
[η]が0.3〜0.6dL/gである。(3) The liquid ethylene / α-olefin copolymer rubber is composed of ethylene and α-olefin having 3 to 20 carbon atoms, and the molar ratio of ethylene to α-olefin is 50/50 to 50/50. 78/22, and the intrinsic viscosity [η] is 0.3 to 0.6 dL / g.
【0021】 〔発明の詳細な説明〕 A.本発明のダンパプーリの弾性体を形成するEOR系
ゴム配合物について、詳細に説明をする。DETAILED DESCRIPTION OF THE INVENTION The EOR rubber compound forming the elastic body of the damper pulley of the present invention will be described in detail.
【0022】EOR系ゴム配合物は、下位特定のEOR
系ポリマーアロイから構成されている未加硫の下記過酸
化物加硫系のゴム配合物であって、加硫物の損失正接
(tanδ)が特定の範囲にあなるようなものである。The EOR rubber compound is a specific EOR
An unvulcanized peroxide-vulcanized rubber compound comprising an unvulcanized polymer alloy as described below, wherein the loss tangent (tan δ) of the vulcanized product falls within a specific range.
【0023】[I]EOR系ポリマーアロイ 本発明で用いられるEOR系ポリマーアロイは、特定の
エチレン・α−オレフィン・非共役ジエン共重合体ゴム
(「三元系EOR」と略す。)(A)と、特定の液状エ
チレン・α−オレフィン共重合体ゴム(「液状二元系E
OR」と略す。)(B)とから構成される。 [I] EOR Polymer Alloy The EOR polymer alloy used in the present invention is a specific ethylene / α-olefin / non-conjugated diene copolymer rubber (abbreviated as “ternary EOR”) (A) And a specific liquid ethylene / α-olefin copolymer rubber (“Liquid binary E
OR ”. ) And (B).
【0024】三元系EOR(A) 上記三元系EOR(A)は、エチレンと炭素原子数3〜
20のα−オレフィンと非共役ジエンとからなる高分子
量のゴムである。 Ternary EOR (A) The above ternary EOR (A) is composed of ethylene and C3-C3.
It is a high molecular weight rubber comprising an α-olefin of 20 and a non-conjugated diene.
【0025】この三元系EOR(A)は、エチレンとα
−オレフィンとのモル比[エチレン/α−オレフィン]
が60/40〜73/27、好ましくは65/35〜7
0/30である。上記モル比が60/40未満になる
と、得られる加硫ゴムの強度が低下する傾向がある。一
方、上記モル比が73/27を超えると、得られる加硫
ゴムの低温柔軟性が低下する傾向がある。This ternary EOR (A) is composed of ethylene and α
-Molar ratio with olefin [ethylene / α-olefin]
Is 60/40 to 73/27, preferably 65/35 to 7
0/30. When the above molar ratio is less than 60/40, the strength of the obtained vulcanized rubber tends to decrease. On the other hand, when the above molar ratio exceeds 73/27, the obtained vulcanized rubber tends to have low-temperature flexibility.
【0026】上記の炭素原子数3〜20のα−オレフィ
ンとしては、具体的には、プロピレン、ブテン−1、ヘ
キセン−1、ペンテン−1、4−メチルペンテン−1、
ヘプテン−1、オクテン−1、ノネン−1、デセン−
1、ウンデセン−1、ドデセン−1、トリデセン−1、
テトラデセン−1、ペンタデセン−1、ヘキサデセン−
1、ヘプタデセン−1、オクタデセン−1、ノナデセン
−1、エイコセン−1などが挙げられる。これらのα−
オレフィンは、単独でまたは組み合わせて用いられる。
これらの中では、特にプロピレンが好ましい。Examples of the α-olefin having 3 to 20 carbon atoms include propylene, butene-1, hexene-1, pentene-1, 4-methylpentene-1,
Heptene-1, octene-1, nonene-1, decene-
1, undecene-1, dodecene-1, tridecene-1,
Tetradecene-1, pentadecene-1, hexadecene-
1, heptadecene-1, octadecene-1, nonadecene-1, eicosene-1 and the like. These α-
Olefins are used alone or in combination.
Of these, propylene is particularly preferred.
【0027】上記の非共役ジエンとしては、具体的に
は、5−エチリデン−2−ノルボルネンが用いられる。
また、上記三元系EOR(A)は、非共役ジエン含量の
一指標であるヨウ素価が10〜40、好ましくは15〜
25である。上記ヨウ素価が10未満になると、得られ
るゴム組成物は、加硫速度が遅くなる傾向がある。一
方、上記ヨウ素価が40を超えると、得られる加硫ゴム
の耐熱性が低下する傾向がある。As the non-conjugated diene, specifically, 5-ethylidene-2-norbornene is used.
The ternary EOR (A) has an iodine value of 10 to 40, preferably 15 to 40, which is an index of the non-conjugated diene content.
25. When the iodine value is less than 10, the obtained rubber composition tends to have a low vulcanization rate. On the other hand, when the iodine value exceeds 40, the heat resistance of the obtained vulcanized rubber tends to decrease.
【0028】上記三元系EORは、分子量分布指数(M
W /Mn )が4未満である。このような分子量分布を有
する高分子量の三元系EOR(A)を用いることによっ
て、機械的強度特性、耐動的疲労性に優れた加硫ゴムを
提供することができる。The ternary EOR has a molecular weight distribution index (M
W / Mn ) is less than 4. By using a high molecular weight ternary EOR (A) having such a molecular weight distribution, a vulcanized rubber excellent in mechanical strength characteristics and dynamic fatigue resistance can be provided.
【0029】また、上記三元系EOR(A)は、極限粘
度[η]が2.7〜5.0dL/g、好ましくは3.5
〜4.5dL/gである。上記極限粘度[η]が2.7
dL/g未満になると、耐久性が低下傾向がある。一
方、上記極限粘度[η]が5.0dL/gを超えると、
ポリマー合成の生産性が低下する傾向がある。極限粘度
[η]が上記のような範囲にある三元系EORを用いる
と、耐動的疲労性に優れた加硫ゴムを得ることができ
る。The ternary EOR (A) has an intrinsic viscosity [η] of 2.7 to 5.0 dL / g, preferably 3.5.
44.5 dL / g. The intrinsic viscosity [η] is 2.7.
If it is less than dL / g, the durability tends to decrease. On the other hand, when the intrinsic viscosity [η] exceeds 5.0 dL / g,
The productivity of polymer synthesis tends to decrease. When a ternary EOR having an intrinsic viscosity [η] in the above range is used, a vulcanized rubber having excellent dynamic fatigue resistance can be obtained.
【0030】上記のような三元系EORは、たとえば特
公昭59−14497号公報に記載されている方法によ
り製造することができる。すなわち、チーグラー触媒の
存在下に、水素を分子量調節剤として用い、エチレンと
炭素原子数3〜20のα−オレフィンとジエンとを共重
合することにより、三元系EORを得ることができる。The above ternary EOR can be produced, for example, by the method described in JP-B-59-14497. That is, a ternary EOR can be obtained by copolymerizing ethylene, an α-olefin having 3 to 20 carbon atoms, and a diene in the presence of a Ziegler catalyst using hydrogen as a molecular weight regulator.
【0031】液状二元系EOR(B) 上記液状二元系EOR(B)は、エチレンと炭素原子数
3〜20のα−オレフィンとからなる低分子量のランダ
ム共重合体であり、ジエン成分を含まない。 Liquid Binary EOR (B) The liquid binary EOR (B) is a low molecular weight random copolymer composed of ethylene and an α-olefin having 3 to 20 carbon atoms, and has a diene component. Not included.
【0032】上記の液状エチレン・α−オレフィン共重
合体は、エチレンと炭素原子数3〜20のα−オレフィ
ンとのランダム共重合体である。上記の炭素原子数3〜
20のα−オレフィンとしては、上記三元系EOR
(A)に例示のものを使用でき、同様に、これらの中で
は、特に、プロピレンが好ましい。The above liquid ethylene / α-olefin copolymer is a random copolymer of ethylene and an α-olefin having 3 to 20 carbon atoms. The above number of carbon atoms 3 to
As the α-olefin of No. 20, the above ternary EOR
(A) Examples can be used, and among these, propylene is particularly preferable.
【0033】本発明においては、上記高分子量の三元系
EOR(A)に、耐熱性、機械的強度特性、耐動的疲労
性等の向上効果を担わせ、一方、低分子量の液状エチレ
ン・α−オレフィン共重合体(B)には、耐熱老化性、
加工性(流動性)の向上効果を担わせるように、品質設
計した。In the present invention, the high molecular weight ternary EOR (A) is made to have an effect of improving heat resistance, mechanical strength characteristics, dynamic fatigue resistance and the like, while low molecular weight liquid ethylene / α is used. -The olefin copolymer (B) has heat aging resistance,
The quality was designed so that the workability (fluidity) could be improved.
【0034】しかしながら、単にバイモーダルな、すな
わち2つのモードを有する分子量分布を示す、高分子量
成分と低分子量成分とからなるEOR系ポリマーアロイ
では、高分子量成分による耐熱性、機械的強度特性、耐
動的疲労性等の物性の向上効果の割合と、低分子量成分
による加工性(流動性)等の向上効果の割合とが綱引き
の関係にあるため、例えば低分子量成分を多くして加工
性に優れていても、耐疲労性というような物性が飛躍的
に向上した加硫ゴムを提供し得ることはできない。However, the EOR-based polymer alloy composed of a high molecular weight component and a low molecular weight component, which is simply bimodal, that is, exhibits a molecular weight distribution having two modes, has heat resistance, mechanical strength characteristics, and dynamic resistance due to the high molecular weight component. Of the effect of improving physical properties such as mechanical fatigue and the ratio of the effect of improving workability (fluidity) due to low molecular weight components are in a tug-of-war relationship. However, it is not possible to provide a vulcanized rubber whose physical properties such as fatigue resistance are dramatically improved.
【0035】そこで、本発明者らは、この低分子量成分
について、さらに鋭意研究したところ、バイモーダルな
分子量分布を示すEOR系ポリマーアロイから加硫ゴム
を得た際に、加硫ゴムを構成する低分子量成分が、ポリ
マーとして架橋されていないことが必要であることを見
出した。すなわち、過酸化物加硫系であっても架橋され
ない程度の分子量であることが必要で、かつ、過酸化物
加硫剤との架橋反応性がアップするジエンを有しない液
状EORであることが必要であることを見出した。低分
子量成分が架橋されると、本発明の目的である高ダンピ
ング特性を得ることができ難くなる。The inventors of the present invention have further studied the low molecular weight component, and found that when a vulcanized rubber was obtained from an EOR-based polymer alloy having a bimodal molecular weight distribution, the vulcanized rubber was constituted. It has been found that low molecular weight components need not be crosslinked as a polymer. That is, it is necessary that the liquid EOR has a molecular weight that does not crosslink even in a peroxide vulcanization system, and that does not have a diene that increases the crosslinking reactivity with a peroxide vulcanizing agent. I found it necessary. When the low molecular weight component is crosslinked, it becomes difficult to obtain the high damping property which is the object of the present invention.
【0036】本発明で用いられる液状二元系EOR
(B)のエチレンとα−オレフィンとのモル比が50/
50〜78/22モル%、好ましくは50/50〜70
/30、さらに好ましくは50/50〜60/40の範
囲内である。上記モル比が上記のような範囲にある液状
二元系EORは、熱安定性が良好であるため、上記のよ
うな高分子量の三元系EOR(A)との混練り操作中に
減量するようなことはなく、また成形時に炭化して成形
品を汚染することもない。Liquid binary EOR used in the present invention
The molar ratio of ethylene and α-olefin of (B) is 50 /
50-78 / 22 mol%, preferably 50 / 50-70
/ 30, more preferably in the range of 50/50 to 60/40. Since the liquid binary EOR having the above molar ratio in the above range has good thermal stability, the liquid binary EOR is reduced during the kneading operation with the high molecular weight ternary EOR (A) as described above. This does not occur, and there is no carbonization at the time of molding to contaminate the molded article.
【0037】上記液状二元系EOR(B)は、極限粘度
[η]が0.3〜0.6dL/g、好ましくは0.30
〜0.45dL/gである。上記極限粘度[η]が上記
範囲を外れると、ダンパプーリに要求される減衰性(ダ
ンピング特性)を得難い。The liquid binary EOR (B) has an intrinsic viscosity [η] of 0.3 to 0.6 dL / g, preferably 0.30 dL / g.
0.40.45 dL / g. If the intrinsic viscosity [η] is out of the above range, it is difficult to obtain the damping property (damping property) required for the damper pulley.
【0038】その理由は、極限粘度が0.6を超える分
子量の場合は、低分子量成分のほとんどが架橋されてい
ると推定され、動的な歪に対して緩和する性質(減衰
性)を失ってしまう。本発明の範囲にある極限粘度示す
分子量の場合には、それぞれの分子が加硫ゴム中で自由
に動けるため、減衰性に寄与することができる。なお、
オイル程度に極限粘度(分子量)が小さくニュートン粘
性を示す場合は、減衰性を示さない。The reason is that when the intrinsic viscosity exceeds 0.6, most of the low molecular weight components are presumed to be cross-linked and lose the property (damping property) of relaxing to dynamic strain. Would. In the case of a molecular weight showing an intrinsic viscosity falling within the range of the present invention, each molecule can move freely in the vulcanized rubber, which can contribute to the damping property. In addition,
When the intrinsic viscosity (molecular weight) is as low as that of oil, and shows Newtonian viscosity, it does not show damping.
【0039】即ち、オイルと同等の可塑化効果(硬度低
下作用)を有し、かつ、非ニュートン粘性を示す極限粘
度(分子量)の範囲にあって、はじめてダンパプーリに
要求されるダンピング特性が発現される。また、極限粘
度(分子量)が高すぎると液状二元系EORによる加工
性(流動性)等の向上効果を得難い。That is, it has a plasticizing effect (hardness lowering effect) equivalent to that of oil and is in the range of the intrinsic viscosity (molecular weight) showing non-Newtonian viscosity, and the damping pulley required for the damper pulley is first exhibited. You. On the other hand, if the intrinsic viscosity (molecular weight) is too high, it is difficult to obtain the effect of improving the processability (fluidity) of the liquid binary EOR.
【0040】上記のような液状エチレン・α−オレフィ
ン共重合体は、たとえば特公平2−1163号公報に記
載されている方法により製造することができる。すなわ
ち、チーグラー触媒の存在下に、水素を分子量調節剤と
して用い、エチレンと炭素原子数3〜20のα−オレフ
ィンとをランダム共重合することにより、液状エチレン
・α−オレフィン共重合体を得ることができる。The above liquid ethylene / α-olefin copolymer can be produced, for example, by the method described in Japanese Patent Publication No. 2-1163. That is, in the presence of a Ziegler catalyst, hydrogen is used as a molecular weight regulator, and ethylene and an α-olefin having 3 to 20 carbon atoms are randomly copolymerized to obtain a liquid ethylene / α-olefin copolymer. Can be.
【0041】EOR系ポリマーアロイの製造 本発明で用いられるEOR系ポリマーアロイ[I]で
は、高分子量の三元系EOR(A)は、三元系EOR
(A)および液状二元系EOR(B)の合計量100%
に対して80〜60%の割合で存在し、低分子量の液状
エチレン・α−オレフィン共重合体(B)は、上記
(A)および(B)の合計量100%に対して20〜4
0%の割合で存在する。 Production of EOR Polymer Alloy In the EOR polymer alloy [I] used in the present invention, the ternary EOR (A) having a high molecular weight is converted into a ternary EOR.
(A) and liquid binary EOR (B) total amount 100%
And the low molecular weight liquid ethylene / α-olefin copolymer (B) is present in an amount of 20 to 4% based on 100% of the total amount of the above (A) and (B).
Present at 0% rate.
【0042】上記のようなEOR系ポリマーアロイ
[I]は、ムーニー粘度ML1+4 (100℃)が通常8
0〜150、好ましくは90〜130であり、かつ、分
子量4500〜10000(極限粘度[η]0.3〜
0.6dL/gからの換算値)のEOR系ポリマーアロ
イのヨウ素価(IV1 )と分子量4,500〜10,0
00のEOR系ポリマーアロイのヨウ素価(IV2 )と
の比(IV1 /IV2 )が通常0.1以下、好ましくは
0である。ムーニー粘度ML1+4 (100℃)および上
記のヨウ素価の比(IV1 /IV2 )が上記のような範
囲内にあるEOR系ポリマーアロイ[I]は、バンバリ
ーミキサーなどによる混練性に優れている。本発明で用
いられるEOR系ポリマーアロイ[I]は、三元系EO
R(A)の溶液または懸濁液と、液状エチレン・α−オ
レフィンの溶液または懸濁液とを混合した後、固体状物
を回収することにより得ることができる。また、最初に
三元系EOR(A)または液状二元系EOR(B)のい
ずれかを重合によって得、さらにその重合体の存在下
で、他の成分を重合によって得る、いわゆる多段重合の
方式によっても本発明のEOR系ポリマーアロイ[I]
を得ることができる。The EOR polymer alloy [I] as described above has a Mooney viscosity ML 1 + 4 (100 ° C.) of usually 8
0 to 150, preferably 90 to 130, and a molecular weight of 4500 to 10000 (intrinsic viscosity [η] 0.3 to
Iodine value (IV 1 ) and molecular weight of 4,500-10,0 of the EOR-based polymer alloy (converted from 0.6 dL / g).
The ratio (IV 1 / IV 2 ) of the 00 to the iodine value (IV 2 ) of the EOR polymer alloy is usually 0.1 or less, preferably 0. The EOR polymer alloy [I] having the Mooney viscosity ML 1 + 4 (100 ° C.) and the above iodine value ratio (IV 1 / IV 2 ) within the above range is excellent in kneading properties using a Banbury mixer or the like. ing. The EOR polymer alloy [I] used in the present invention is a ternary EO
It can be obtained by mixing a solution or suspension of R (A) and a solution or suspension of liquid ethylene / α-olefin, and then collecting a solid. In addition, a so-called multi-stage polymerization system in which either a ternary EOR (A) or a liquid binary EOR (B) is first obtained by polymerization, and other components are obtained by polymerization in the presence of the polymer. The EOR polymer alloy [I] of the present invention
Can be obtained.
【0043】[II]加硫剤 上記加硫剤としては、基本的には、過酸化物を使用する
が、硫黄を併用してもよい。本発明ではEOR系ゴム配
合物が過酸化物加硫系とするためである。 [II] Vulcanizing Agent As the vulcanizing agent, a peroxide is basically used, but sulfur may be used in combination. This is because, in the present invention, the EOR rubber compound is a peroxide vulcanized system.
【0044】過酸化物としては、ジクミルパーオキサイ
ド(DCP)、1,3ビス(第三ブチルペルオキシイソ
プロピル)ベンゼン、2,5−ジメチル−2,5−ジ
(第三ブチルペルオキシ)ヘキサン−3、1,1−ビス
(第三ブチルペルオキシ)−3,3,5−トリメチルシ
クロヘキサン、n−ブチル−4,4−ビス(第三ブチル
ペルオキシ)バレレート、2,5−ジメチル−2,5−
ジ(ベンゾイルペルオキシ)ヘキサン、1,1−ジ(第
三ブチルペルオキシ)シクロヘキサン等を挙げることが
できる。As the peroxide, dicumyl peroxide (DCP), 1,3 bis (tert-butylperoxyisopropyl) benzene, 2,5-dimethyl-2,5-di (tert-butylperoxy) hexane-3 1,1-bis (tert-butylperoxy) -3,3,5-trimethylcyclohexane, n-butyl-4,4-bis (tert-butylperoxy) valerate, 2,5-dimethyl-2,5-
Examples thereof include di (benzoylperoxy) hexane and 1,1-di (tert-butylperoxy) cyclohexane.
【0045】当該過酸化物は、上記EOR系ポリマーア
ロイ[I]100部に対して、1〜15部、好ましくは
3〜10部の割合で用いられる。The peroxide is used in a proportion of 1 to 15 parts, preferably 3 to 10 parts, per 100 parts of the EOR polymer alloy [I].
【0046】なお、イオウを併用する場合、イオウは、
上記ポリマーアロイ[I]100部に対して、0.1〜
1部、好ましくは0.1〜0.5部の割合で用いられ
る。When sulfur is used in combination, the sulfur is
0.1 to 100 parts of the polymer alloy [I]
1 part, preferably 0.1 to 0.5 part.
【0047】本発明では、上記加硫剤は、未加硫のゴム
配合物中に予め配合させておくが、当該ゴム配合物の加
硫直前に添加してもよい。In the present invention, the vulcanizing agent is previously compounded in an unvulcanized rubber compound, but may be added immediately before vulcanization of the rubber compound.
【0048】[III ]その他の配合剤 本発明のEOR系ゴム配合物に、上記EOR系ポリマー
アロイ[I]及び加硫剤[II]他に、EOR等の加硫ゴ
ム成形体の製造において従来より広く一般に用いられて
いるカーボンブラック(1) 、軟化剤(2) 、亜鉛華等の配
合剤を、本発明の目的を損なわない範囲で用いることが
できる。 [III] Other compounding agents In addition to the EOR-based polymer alloy [I] and the vulcanizing agent [II], the EOR-based rubber compound of the present invention may be used in the production of vulcanized rubber moldings such as EOR. Compounding agents such as carbon black (1), softener (2), and zinc white, which are more generally used, can be used as long as the object of the present invention is not impaired.
【0049】(1) 上記カーボンブラックとしては、ゴム
用のカーボンブラックであれば特にその種類は問わない
が、特にHAF、MAF、FEF、GPF等のファーネ
スカーボンブラックが好ましい。(1) The type of carbon black is not particularly limited as long as it is carbon black for rubber. Furnace carbon black such as HAF, MAF, FEF and GPF is particularly preferable.
【0050】本発明に係るEOR系ゴム配合物において
は、カーボンブラックは、上記EOR系ポリマーアロイ
[I]100部に対して、通常、40〜120部の範囲
内で用いられる。カーボンブラックの配合量が40部未
満になると、得られる加硫ゴムの硬さ及び強度が低下す
る傾向がある。一方、カーボンブラックの配合量が12
0部を超えると、得られるゴム組成物は、加工性が低下
し、カーボンブラックの分散不良等が生じる傾向があ
る。本発明では、カーボンブラックは、未加硫のゴム組
成物中に存在しているが、上記EOR系ポリマーアロイ
を加硫する際に使用してもよい。In the EOR rubber compound according to the present invention, carbon black is generally used in the range of 40 to 120 parts based on 100 parts of the above EOR polymer alloy [I]. If the amount of carbon black is less than 40 parts, the resulting vulcanized rubber tends to have reduced hardness and strength. On the other hand, when the compounding amount of carbon black is 12
If the amount exceeds 0 parts, the obtained rubber composition tends to have low processability and poor dispersion of carbon black. In the present invention, the carbon black is present in the unvulcanized rubber composition, but may be used when vulcanizing the EOR polymer alloy.
【0051】(2) 上記軟化剤としては、通常、ゴムに用
いられる軟化剤が用いられるが、具体的には、プロセス
オイル、潤滑油、パラフィン、流動パラフィン、石油ア
スファルト、ワセリン等の石油系軟化剤;コールター
ル、コールタールピッチ等のコールタール系軟化剤;ヒ
マシ油、アマニ油、ナタネ油、ヤシ油等の脂肪油系軟化
剤;サブ;密ロウ、カルナウバロウ、ラノリン等のロウ
類;リシノール酸、パルミチン酸、ステアリン酸バリウ
ム、ステアリン酸カルシウム、ラウリン酸亜鉛等の脂肪
酸および脂肪酸塩;石油樹脂、アタクチックポリプロピ
レン、クマロンインデン樹脂等の合成高分子物質等が用
いられる。なかでも石油系軟化剤が好ましく用いられ、
特にプロセスオイルが好ましく用いられる。(2) As the above-mentioned softening agent, a softening agent usually used for rubber is used, and specifically, a petroleum softening agent such as process oil, lubricating oil, paraffin, liquid paraffin, petroleum asphalt, petrolatum, etc. Coal tar softeners such as coal tar and coal tar pitch; fatty oil softeners such as castor oil, linseed oil, rapeseed oil and coconut oil; sub; waxes such as beeswax, carnauba wax and lanolin; ricinoleic acid Fatty acids and fatty acid salts such as palmitic acid, barium stearate, calcium stearate and zinc laurate; and synthetic high molecular substances such as petroleum resins, atactic polypropylene, and coumarone indene resins. Among them, petroleum softeners are preferably used,
Particularly, process oil is preferably used.
【0052】本発明に係るEOR系ゴム配合物(未加硫
の配合ゴム)は、たとえば以下の方法により調製され
る。すなわち、バンバリーミキサー等のミキサー類を用
いて、上記EOR系ポリマーアロイおよび軟化剤を30
〜170℃の温度で3〜10分間混練し、次いで、オー
ブンロール等のロール類を用いて、加硫剤としてイオ
ウ、およびカーボンブラック、必要に応じて加硫促進剤
または加硫助剤を追加混合し、ロール温度40〜80℃
で5〜30分間混練した後、混練物を押出し、リボン状
またはシート状の配合ゴムを調製する。The EOR rubber compound (unvulcanized compound rubber) according to the present invention is prepared, for example, by the following method. That is, the EOR-based polymer alloy and the softener were mixed with a mixer such as a Banbury mixer.
Kneaded at a temperature of ~ 170 ° C for 3 to 10 minutes, and then, using rolls such as an oven roll, add sulfur and carbon black as a vulcanizing agent, and if necessary, a vulcanization accelerator or a vulcanization aid. Mix, roll temperature 40-80 ° C
After kneading for 5 to 30 minutes, the kneaded product is extruded to prepare a ribbon-shaped or sheet-shaped compounded rubber.
【0053】本発明のEOR系ゴム配合物は、加硫物の
損失正接(tan δ)が0.20〜0.35になるような
組成を有している。The EOR rubber compound of the present invention has a composition such that the loss tangent (tan δ) of the vulcanizate is 0.20 to 0.35.
【0054】加硫ゴムの製造 本発明に係るEOR系ゴム配合物から加硫ゴムを得るに
は、上記の未加硫配合ゴムを意図する弾性体の形状に成
形した後加硫を行えばよい。 Production of Vulcanized Rubber In order to obtain a vulcanized rubber from the EOR-based rubber compound according to the present invention, the unvulcanized compounded rubber is molded into an intended elastic body and then vulcanized. .
【0055】なお、加硫接着タイプの場合は、未加硫の
状態で、ダンパマスとプーリの間に注入して成形後、加
硫する。In the case of the vulcanized adhesive type, in an unvulcanized state, it is injected between a damper mass and a pulley, molded, and then vulcanized.
【0056】[0056]
【発明の効果】本発明に係るダンパプーリは、その弾性
体を形成する、EOR系ゴム配合物として、特開平6−
1891号公報に記載されている特定の三元系EOR
(A)と特定の液状二元系EOR(B)とからなるポリ
マーアロイをベースとするものにおいて、加硫系を特定
するとともに、液状EOR系ゴムとして極限粘度を高い
方シフトさせたものを使用することにより、後述の実施
例・比較例で支持される如く、顕著な作用・効果を奏す
る。The damper pulley according to the present invention has an EOR rubber compound forming an elastic body, which is disclosed in
Certain ternary EORs described in US Pat.
A polymer based on a polymer alloy consisting of (A) and a specific liquid binary EOR (B), in which the vulcanization system is specified, and a liquid EOR rubber whose intrinsic viscosity is shifted to a higher one is used. By doing so, a remarkable action and effect can be obtained as supported by the following Examples and Comparative Examples.
【0057】即ち、本発明のダンパプーリは、高温雰囲
気下でも安定した防振性能を発揮でき、また、単純圧入
タイプのダンパプーリにおいて、ダンパマス及び/また
はプーリと弾性体との間の結合性に問題が発生し難い。That is, the damper pulley of the present invention can exhibit a stable vibration-proof performance even in a high-temperature atmosphere. In a simple press-fit type damper pulley, there is a problem in the damper mass and / or the coupling between the pulley and the elastic body. It is unlikely to occur.
【0058】[0058]
【実施例】以下、本発明の効果を確認するために、比較
例とともに実施例について説明をする。本発明は、これ
ら実施例に限定されるものではない。EXAMPLES In order to confirm the effects of the present invention, examples will be described together with comparative examples. The present invention is not limited to these examples.
【0059】A.実施例・比較例に使用した基本配合処
方は、下記の通りである。A. The basic formulation used in the examples and comparative examples is as follows.
【0060】過酸化物加硫系EOR配合処方 ポリマーアロイ 160部 ステアリン酸 1部 亜鉛華 5部 カーボンブラック(FEF) 60部 老化防止剤 2部 有機過酸化物* 5.5部 *DCP40wt%含有品 また、参照例に使用した基本配合処方は、下記の通りで
ある。 Peroxide vulcanized EOR compounded polymer alloy 160 parts Stearic acid 1 part Zinc white 5 parts Carbon black (FEF) 60 parts Antioxidant 2 parts Organic peroxide * 5.5 parts * DCP 40 wt% content The basic formulation used in the reference example is as follows.
【0061】硫黄加硫系EOR配合処方 ポリマーアロイ 160部 ステアリン酸 1部 亜鉛華 5部 カーボンブラック(FEF) 60部 老化防止剤 2部 硫黄 4部 加硫促進剤 3.5部 上記基本配合処方において、表1に示す仕様の各ポリマ
ーアロイ(パラフィンオイル含有マスターバッチまたは
パラフィンオイル非含有タイプ)を使用したゴム配合物
をバンバリーミキサーで混練した。 Formulation of sulfur vulcanized EOR compound 160 parts Polymer alloy 1 part Stearic acid 1 part Zinc white 5 part Carbon black (FEF) 60 parts Antioxidant 2 parts Sulfur 4 parts Vulcanization accelerator 3.5 parts A rubber compound using each polymer alloy (paraffin oil-containing masterbatch or paraffin oil-free type) having the specifications shown in Table 1 was kneaded with a Banbury mixer.
【0062】なお、ポリマーアロイは、高分子量成分
(A成分)は下記仕様のものを使用し、該高分子量成分
(A成分)100部に対して、表示の低分子量成分(B
成分)とパラフィン系オイルの合計量が60部となるよ
うに配合したものを使用した(表1参照)。As the polymer alloy, a high molecular weight component (component A) having the following specifications was used, and 100 parts of the high molecular weight component (component A) was added to the low molecular weight component (B
Component) and paraffin-based oil were used so that the total amount was 60 parts (see Table 1).
【0063】<A成分仕様>エチレン/α−オレフィ
ン:68/32、分子量分布指数(MW /Mn ):3.
7、極限粘度[η]:4.0dL/g、ヨウ素価:22[0063] <A Component Specification> ethylene / alpha-olefin: 68/32, molecular weight distribution index (M W / M n): 3.
7, intrinsic viscosity [η]: 4.0 dL / g, iodine value: 22
【0064】[0064]
【表1】 [Table 1]
【0065】こうした得られた混練物を使用して、下記
各試験を試験片を調製して、試験を行った。 B.試験方法 各ポリマーアロイ、加硫ゴムについての試験方法は、以
下の通りである。Using the obtained kneaded material, a test piece was prepared for each of the following tests and tested. B. Test method The test method for each polymer alloy and vulcanized rubber is as follows.
【0066】[1]分子量分布指数(MW /Mn ) 分子量分布指数(MW /Mn )の測定は、GPC(ゲル
パミエーションクロマトグラフィー)法(例えば、「ゲ
ルパミエーションクロマトグラフィー」武内著、丸善株
式会社発行)に準じて下記のとおり行った。[0066] [1] Measurement of molecular weight distribution index (M W / M n) molecular weight distribution index (M W / M n) is, GPC (gel Pami instantiation chromatography) (e.g., "gel Pami instantiation chromatography" Takeuchi Author, published by Maruzen Co., Ltd.).
【0067】分子量既知の標準ポリスチレン(東ソー
(株)製、単分散ポリスチレン)を使用して分子量Mと
そのGPC(Gel Permeation Chro
matography)カウントを測定し、分子量Mと
溶離体積EV(ElutionVolume)との相関
図較正曲線を作成する。このときのポリスチレン濃度
は、0.02%とする。Using standard polystyrene of known molecular weight (monodisperse polystyrene, manufactured by Tosoh Corporation), the molecular weight M and its GPC (Gel Permeation Chromium) were measured.
The measurement graph is measured and a correlation curve between the molecular weight M and the elution volume EV (ElutionVolume) is prepared. At this time, the polystyrene concentration is set to 0.02%.
【0068】[3]硬さ試験 硬さ試験は、JIS K 6301(1989年)に準
拠して行い(加硫条件:170℃×10分)、スプリン
グ硬さ(JIS A硬度)を測定した。[3] Hardness Test A hardness test was performed according to JIS K 6301 (1989) (vulcanization condition: 170 ° C. × 10 minutes), and a spring hardness (JIS A hardness) was measured.
【0069】[4]引張試験 引張試験は、JIS K 6301(1989年)に準
拠して行い(加硫条件:170℃×10分)、引張強さ
(TB )、伸び(EB )、及び、100%モジュラス
(M100 )を測定した。[4] Tensile test The tensile test was carried out in accordance with JIS K 6301 (1989) (vulcanization conditions: 170 ° C. × 10 minutes), and the tensile strength (T B ), elongation (E B ), and it was measured at 100% modulus (M 100).
【0070】[5]動的粘弾性試験 動的粘弾性試験は、レオロジー社性の粘弾性試験機(D
VE−V4型)を用いて、測定温度25℃、周波数15
Hz、100Hz及び歪み率0.5%、1.8%の条件
で行い、動的剪断弾性率(dyn/cm2 )と動的損失弾性率
(dyn/cm2 )を求め、損失正接tan δ(振動減衰性の指
標)を下式により求めた。なお、加硫条件は、上記と同
様、170℃×10分とした。[5] Dynamic viscoelasticity test The dynamic viscoelasticity test was performed using a viscoelasticity tester (D
VE-V4), measuring temperature 25 ° C, frequency 15
The dynamic shear modulus (dyn / cm 2 ) and the dynamic loss modulus (dyn / cm 2 ) were determined under the conditions of Hz, 100 Hz and a strain rate of 0.5% and 1.8%, and the loss tangent tan δ was obtained. (Index of vibration damping) was determined by the following equation. The vulcanization conditions were 170 ° C. × 10 minutes as in the above.
【0071】 E* =E’+iE” tan δ=E”/E’ (E* :動的複素弾性率、E’:動的剪断弾性率、
E”:動的損失弾性率) [6]耐熱試験 耐熱試験は、表示の条件で行い、JIS K 6301
(1989年)に準拠して、加熱処理(120℃×70
h)後の、硬度変化(△H)及びへたり(CS)を求め
た。E * = E ′ + iE ″ tan δ = E ″ / E ′ (E * : dynamic complex elastic modulus, E ′: dynamic shear elastic modulus,
E ”: dynamic loss elastic modulus) [6] Heat resistance test The heat resistance test was performed under the conditions shown in JIS K6301.
(1989), heat treatment (120 ° C × 70
h) After that, the change in hardness (ΔH) and set (CS) were determined.
【0072】C.試験結果及び評価 上記各記試験を行った結果を示す表2〜3から、液状二
元EORの極限粘度[η]が本発明の範囲内にある場合
は、損失正接(tan δ)が0.20以上と高く、減衰性
(ダンピング特性)に優れていることがより明瞭に分か
る。C. Test Results and Evaluation From Tables 2 and 3 showing the results of the above tests, when the intrinsic viscosity [η] of the liquid binary EOR is within the range of the present invention, the loss tangent (tan δ) is 0. It is clearly seen that it is as high as 20 or more and excellent in damping property (damping property).
【0073】即ち、高分子量成分のみで低分子量成分を
含まないEOR−2を用いた比較例1、極限粘度[η]
が0.3未満のEOR−3・4を用いた比較例2・3及
び極限粘度[η]が0.70を越えるEOR−7を用い
た比較例4、低分子量成分が過少であるEOR−10を
用いた比較例5、更には、低分子量成分が三元系EOR
であるEOR−11を用いた比較例6は、いずれも損失
正接(tan δ)が0.20未満である(表3参照)。That is, Comparative Example 1 using EOR-2 containing only a high molecular weight component and no low molecular weight component, the limiting viscosity [η]
Comparative Example 2.3 using EOR-3.4 having a molecular weight of less than 0.3 and Comparative Example 4 using EOR-7 having an intrinsic viscosity [η] of more than 0.70, and EOR- having an insufficient low molecular weight component. Comparative Example 5 using No. 10, and further, the low molecular weight component was a ternary EOR
In Comparative Example 6 using EOR-11, the loss tangent (tan δ) was less than 0.20 (see Table 3).
【0074】また、表2から、本発明の弾性体が過酸化
物加硫系配合物で形成されたダンパプーリ(実施例1)
は、硫黄加硫系配合物で形成されたダンパプーリ(参照
例)に比して、ダンピング特性が余り劣らず、格段に耐
熱性に優れていることが分かる。From Table 2, it can be seen that a damper pulley in which the elastic body of the present invention was formed of a peroxide-cured compound (Example 1)
It can be seen that, compared to the damper pulley formed of the sulfur vulcanized compound (Reference Example), the damping characteristics are not so inferior and the heat resistance is remarkably excellent.
【0075】[0075]
【表2】 [Table 2]
【0076】[0076]
【表3】 [Table 3]
【図1】本発明を適用するダンパプーリの一例を示す判
断面図FIG. 1 is a judgment view showing an example of a damper pulley to which the present invention is applied.
【符号の説明】 12 ダンパマス(ハブ) 14 プーリ 16 弾性体 18 ダンパプーリ[Description of Signs] 12 Damper mass (hub) 14 Pulley 16 Elastic body 18 Damper pulley
フロントページの続き (72)発明者 竹内 勝政 愛知県西春日井郡春日町大字落合字長畑1 番地 豊田合成株式会社内 (72)発明者 今井 英幸 愛知県西春日井郡春日町大字落合字長畑1 番地 豊田合成株式会社内 (72)発明者 渡辺 悟美 愛知県西春日井郡春日町大字落合字長畑1 番地 豊田合成株式会社内 (72)発明者 三宅 和俊 愛知県西春日井郡春日町大字落合字長畑1 番地 豊田合成株式会社内 (72)発明者 仲濱 秀斉 千葉県市原市千種海岸3番地 三井石油化 学工業株式会社内(72) Inventor Katsumasa Takeuchi 1 Ochiai Nagahata, Kasuga-cho, Nishi-Kasugai-gun, Aichi Prefecture Inside Toyoda Gosei Co., Ltd. (72) Inventor Hideyuki Imai 1 Nagachi Ochiai, Kasuga-cho, Nishi-Kasugai-gun, Aichi 1 Toyoda Gosei Co., Ltd. Inside the company (72) Inventor Satomi Watanabe 1 at Nagahata, Ochiai, Kasuga-cho, Nishi-Kasugai-gun, Aichi Prefecture Inside of Toyota Kasei Co., Ltd. (72) Inventor Hidenari Nakahama 3 Chigusa Beach, Ichihara City, Chiba Prefecture Mitsui Oil Chemicals Co., Ltd.
Claims (2)
在されてなるダンパプーリにおいて、 前記弾性体が、下記要件(1) 〜(3) を満たすポリマーア
ロイをベースとする過酸化物加硫系ゴム配合物の加硫物
であって、損失正接(tan δ)が0.20〜0.35で
あるもので形成されていることを特徴とするダンパプー
リ。 (1) 前記ポリマーアロイは、エチレン・α−オレフィン
・非共役ジエン共重合体ゴム(A):80〜60重量%
と液状エチレン・α−オレフィン共重合体(B):20
〜40重量%からなる。 (2) 前記エチレン・α−オレフィン・非共役ジエン共重
合体ゴムは、エチレンと炭素原子数3〜20のα−オレ
フィンと非共役ジエンとからなり、かつ、エチレンとα
−オレフィンとのモル比が60/40〜73/27であ
り、分子量分布指数(MW /Mn )が4未満であり、極
限粘度[η]が約2.7〜5.0dL/gであり、ヨウ
素価が10〜40であり、非共役ジエンが5−エチリデ
ン−2−ノルボルネンである。 (3) 前記液状エチレン・α−オレフィン共重合体ゴム
は、エチレンと炭素原子数3〜20のα−オレフィンと
からなり、かつ、エチレンとα−オレフィンとのモル比
が50/50〜78/22であり、極限粘度[η]が
0.3〜0.6dL/gである。1. A damper pulley in which an elastic body is interposed between a damper mass and a pulley, wherein the elastic body is a peroxide vulcanizing system based on a polymer alloy satisfying the following requirements (1) to (3). A damper pulley, which is formed of a vulcanized rubber compound and has a loss tangent (tan δ) of 0.20 to 0.35. (1) The polymer alloy is an ethylene / α-olefin / non-conjugated diene copolymer rubber (A): 80 to 60% by weight
And liquid ethylene / α-olefin copolymer (B): 20
-40% by weight. (2) The ethylene / α-olefin / non-conjugated diene copolymer rubber comprises ethylene, an α-olefin having 3 to 20 carbon atoms and a non-conjugated diene, and comprises ethylene and α.
- the molar ratio of olefin is 60 / 40-73 / 27, the molecular weight distribution index (M W / M n) is less than 4, an intrinsic viscosity [eta] of about 2.7~5.0DL / g The iodine value is 10 to 40, and the non-conjugated diene is 5-ethylidene-2-norbornene. (3) The liquid ethylene / α-olefin copolymer rubber comprises ethylene and an α-olefin having 3 to 20 carbon atoms, and the molar ratio of ethylene to the α-olefin is 50/50 to 78 /. 22, and the intrinsic viscosity [η] is 0.3 to 0.6 dL / g.
単純圧入されてなることを特徴とする請求項1記載のダ
ンパプーリ。2. The damper pulley according to claim 1, wherein the elastic body between the damper mass and the pulley is simply press-fitted.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9002376A JPH10196719A (en) | 1997-01-09 | 1997-01-09 | Damper pulley |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9002376A JPH10196719A (en) | 1997-01-09 | 1997-01-09 | Damper pulley |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH10196719A true JPH10196719A (en) | 1998-07-31 |
Family
ID=11527539
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP9002376A Pending JPH10196719A (en) | 1997-01-09 | 1997-01-09 | Damper pulley |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH10196719A (en) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2000120789A (en) * | 1998-10-16 | 2000-04-25 | Mitsubishi Motors Corp | Damper device |
| JP2001065668A (en) * | 1999-08-27 | 2001-03-16 | Toyoda Gosei Co Ltd | Damper pulley |
| JP2001153209A (en) * | 1999-11-25 | 2001-06-08 | Toyoda Gosei Co Ltd | Damper pulley |
| JP2002213577A (en) * | 2001-01-18 | 2002-07-31 | Toyoda Gosei Co Ltd | Damper pulley |
| JP2002357244A (en) * | 2001-06-04 | 2002-12-13 | Tokai Rubber Ind Ltd | Torsion damper |
| JP2003127879A (en) * | 2001-10-22 | 2003-05-08 | Toyoda Mach Works Ltd | Electric power steering device |
| JP2007112921A (en) * | 2005-10-21 | 2007-05-10 | Mitsui Chemicals Inc | Processing method for continuous organic peroxide crosslinked rubber molded body and crosslinked rubber molded body |
| WO2016199473A1 (en) * | 2015-06-09 | 2016-12-15 | 豊田合成株式会社 | Rubber, and seal component and hose |
| WO2018216567A1 (en) * | 2017-05-23 | 2018-11-29 | 株式会社フコク | Torsional damper |
| CN114825168A (en) * | 2022-04-25 | 2022-07-29 | 北京航天长城卫星导航科技有限公司 | Railway electric power safety monitoring device |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0586236A (en) * | 1991-09-27 | 1993-04-06 | Mitsui Petrochem Ind Ltd | Rubber composition for heat-resistant anti-vibration rubber |
| JPH061891A (en) * | 1992-06-18 | 1994-01-11 | Mitsui Petrochem Ind Ltd | Rubber composition for heat-resistant anti-vibration rubber |
| JPH06264972A (en) * | 1993-03-12 | 1994-09-20 | Mitsubishi Motors Corp | Torsional damper |
| JPH08277884A (en) * | 1995-04-05 | 1996-10-22 | Bridgestone Corp | Torsional damper |
| JPH08285013A (en) * | 1995-04-14 | 1996-11-01 | Nok Megurasutikku Kk | Damper |
| JPH1089409A (en) * | 1996-09-20 | 1998-04-07 | Kinugawa Rubber Ind Co Ltd | Dynamic damper |
-
1997
- 1997-01-09 JP JP9002376A patent/JPH10196719A/en active Pending
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0586236A (en) * | 1991-09-27 | 1993-04-06 | Mitsui Petrochem Ind Ltd | Rubber composition for heat-resistant anti-vibration rubber |
| JPH061891A (en) * | 1992-06-18 | 1994-01-11 | Mitsui Petrochem Ind Ltd | Rubber composition for heat-resistant anti-vibration rubber |
| JPH06264972A (en) * | 1993-03-12 | 1994-09-20 | Mitsubishi Motors Corp | Torsional damper |
| JPH08277884A (en) * | 1995-04-05 | 1996-10-22 | Bridgestone Corp | Torsional damper |
| JPH08285013A (en) * | 1995-04-14 | 1996-11-01 | Nok Megurasutikku Kk | Damper |
| JPH1089409A (en) * | 1996-09-20 | 1998-04-07 | Kinugawa Rubber Ind Co Ltd | Dynamic damper |
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2000120789A (en) * | 1998-10-16 | 2000-04-25 | Mitsubishi Motors Corp | Damper device |
| JP2001065668A (en) * | 1999-08-27 | 2001-03-16 | Toyoda Gosei Co Ltd | Damper pulley |
| JP2001153209A (en) * | 1999-11-25 | 2001-06-08 | Toyoda Gosei Co Ltd | Damper pulley |
| JP2002213577A (en) * | 2001-01-18 | 2002-07-31 | Toyoda Gosei Co Ltd | Damper pulley |
| JP2002357244A (en) * | 2001-06-04 | 2002-12-13 | Tokai Rubber Ind Ltd | Torsion damper |
| JP2003127879A (en) * | 2001-10-22 | 2003-05-08 | Toyoda Mach Works Ltd | Electric power steering device |
| JP2007112921A (en) * | 2005-10-21 | 2007-05-10 | Mitsui Chemicals Inc | Processing method for continuous organic peroxide crosslinked rubber molded body and crosslinked rubber molded body |
| WO2016199473A1 (en) * | 2015-06-09 | 2016-12-15 | 豊田合成株式会社 | Rubber, and seal component and hose |
| WO2018216567A1 (en) * | 2017-05-23 | 2018-11-29 | 株式会社フコク | Torsional damper |
| JP2018197572A (en) * | 2017-05-23 | 2018-12-13 | 株式会社フコク | Torsional damper |
| CN110678669A (en) * | 2017-05-23 | 2020-01-10 | 株式会社富国 | Torsional vibration damper |
| CN114825168A (en) * | 2022-04-25 | 2022-07-29 | 北京航天长城卫星导航科技有限公司 | Railway electric power safety monitoring device |
| CN114825168B (en) * | 2022-04-25 | 2023-06-20 | 北京航天长城卫星导航科技有限公司 | Railway electric power safety monitoring device |
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