JP2001146942A - Transmission belt - Google Patents
Transmission beltInfo
- Publication number
- JP2001146942A JP2001146942A JP33200299A JP33200299A JP2001146942A JP 2001146942 A JP2001146942 A JP 2001146942A JP 33200299 A JP33200299 A JP 33200299A JP 33200299 A JP33200299 A JP 33200299A JP 2001146942 A JP2001146942 A JP 2001146942A
- Authority
- JP
- Japan
- Prior art keywords
- rubber layer
- rubber
- belt
- transmission belt
- dispersed
- 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
- 230000005540 biological transmission Effects 0.000 title claims abstract description 37
- 229920001971 elastomer Polymers 0.000 claims abstract description 144
- 239000005060 rubber Substances 0.000 claims abstract description 121
- 239000000835 fiber Substances 0.000 claims abstract description 37
- 230000006835 compression Effects 0.000 claims abstract description 9
- 238000007906 compression Methods 0.000 claims abstract description 9
- 239000000806 elastomer Substances 0.000 claims description 23
- 239000004711 α-olefin Substances 0.000 claims description 23
- 239000000853 adhesive Substances 0.000 claims description 21
- 230000001070 adhesive effect Effects 0.000 claims description 21
- 239000010419 fine particle Substances 0.000 claims description 18
- 229910010272 inorganic material Inorganic materials 0.000 claims description 8
- 239000011147 inorganic material Substances 0.000 claims description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 5
- 239000000919 ceramic Substances 0.000 claims description 4
- 239000000843 powder Substances 0.000 claims description 4
- 239000005909 Kieselgur Substances 0.000 claims description 3
- 150000001451 organic peroxides Chemical class 0.000 claims description 3
- 239000000463 material Substances 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 12
- 230000003746 surface roughness Effects 0.000 abstract description 7
- 239000004744 fabric Substances 0.000 abstract description 3
- 238000002156 mixing Methods 0.000 abstract description 3
- 239000006185 dispersion Substances 0.000 abstract description 2
- 238000010030 laminating Methods 0.000 abstract description 2
- 239000002245 particle Substances 0.000 abstract 2
- 230000001747 exhibiting effect Effects 0.000 abstract 1
- 239000011368 organic material Substances 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 73
- 229920000459 Nitrile rubber Polymers 0.000 description 10
- -1 polyethylene Polymers 0.000 description 10
- 239000012298 atmosphere Substances 0.000 description 8
- 238000005452 bending Methods 0.000 description 8
- 229920001410 Microfiber Polymers 0.000 description 7
- 229920002681 hypalon Polymers 0.000 description 7
- 239000003658 microfiber Substances 0.000 description 7
- 229920000728 polyester Polymers 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- 229920000742 Cotton Polymers 0.000 description 6
- 238000005299 abrasion Methods 0.000 description 6
- 238000004132 cross linking Methods 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 5
- 239000004760 aramid Substances 0.000 description 5
- 229920006231 aramid fiber Polymers 0.000 description 5
- 238000004073 vulcanization Methods 0.000 description 5
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 4
- 229920003235 aromatic polyamide Polymers 0.000 description 4
- 239000006229 carbon black Substances 0.000 description 4
- 239000011159 matrix material Substances 0.000 description 4
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- 229920002943 EPDM rubber Polymers 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 244000043261 Hevea brasiliensis Species 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 3
- 239000007822 coupling agent Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- 229920000126 latex Polymers 0.000 description 3
- 239000004816 latex Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229920003052 natural elastomer Polymers 0.000 description 3
- 229920001194 natural rubber Polymers 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 150000002978 peroxides Chemical class 0.000 description 3
- 229920001084 poly(chloroprene) Polymers 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 229920003048 styrene butadiene rubber Polymers 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- 239000004636 vulcanized rubber Substances 0.000 description 3
- IPJGAEWUPXWFPL-UHFFFAOYSA-N 1-[3-(2,5-dioxopyrrol-1-yl)phenyl]pyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1=CC=CC(N2C(C=CC2=O)=O)=C1 IPJGAEWUPXWFPL-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
- 239000004593 Epoxy Substances 0.000 description 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 229910052581 Si3N4 Inorganic materials 0.000 description 2
- 239000002174 Styrene-butadiene Substances 0.000 description 2
- 229920006311 Urethane elastomer Polymers 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 208000018747 cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome Diseases 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 229920005558 epichlorohydrin rubber Polymers 0.000 description 2
- 239000003365 glass fiber Substances 0.000 description 2
- 238000005984 hydrogenation reaction Methods 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 238000009958 sewing Methods 0.000 description 2
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 2
- 229910010271 silicon carbide Inorganic materials 0.000 description 2
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 2
- 238000009987 spinning Methods 0.000 description 2
- RRKODOZNUZCUBN-CCAGOZQPSA-N (1z,3z)-cycloocta-1,3-diene Chemical compound C1CC\C=C/C=C\C1 RRKODOZNUZCUBN-CCAGOZQPSA-N 0.000 description 1
- PRBHEGAFLDMLAL-GQCTYLIASA-N (4e)-hexa-1,4-diene Chemical compound C\C=C\CC=C PRBHEGAFLDMLAL-GQCTYLIASA-N 0.000 description 1
- OJOWICOBYCXEKR-KRXBUXKQSA-N (5e)-5-ethylidenebicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(=C/C)/CC1C=C2 OJOWICOBYCXEKR-KRXBUXKQSA-N 0.000 description 1
- KOMNUTZXSVSERR-UHFFFAOYSA-N 1,3,5-tris(prop-2-enyl)-1,3,5-triazinane-2,4,6-trione Chemical compound C=CCN1C(=O)N(CC=C)C(=O)N(CC=C)C1=O KOMNUTZXSVSERR-UHFFFAOYSA-N 0.000 description 1
- IEKHISJGRIEHRE-UHFFFAOYSA-N 16-methylheptadecanoic acid;propan-2-ol;titanium Chemical compound [Ti].CC(C)O.CC(C)CCCCCCCCCCCCCCC(O)=O.CC(C)CCCCCCCCCCCCCCC(O)=O.CC(C)CCCCCCCCCCCCCCC(O)=O IEKHISJGRIEHRE-UHFFFAOYSA-N 0.000 description 1
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- 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 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- BIISIZOQPWZPPS-UHFFFAOYSA-N 2-tert-butylperoxypropan-2-ylbenzene Chemical compound CC(C)(C)OOC(C)(C)C1=CC=CC=C1 BIISIZOQPWZPPS-UHFFFAOYSA-N 0.000 description 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 229910052580 B4C Inorganic materials 0.000 description 1
- 229910052582 BN Inorganic materials 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- 229920000271 Kevlar® Polymers 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- 229920001494 Technora Polymers 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 description 1
- OKKRPWIIYQTPQF-UHFFFAOYSA-N Trimethylolpropane trimethacrylate Chemical compound CC(=C)C(=O)OCC(CC)(COC(=O)C(C)=C)COC(=O)C(C)=C OKKRPWIIYQTPQF-UHFFFAOYSA-N 0.000 description 1
- 229920000561 Twaron Polymers 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- INAHAJYZKVIDIZ-UHFFFAOYSA-N boron carbide Chemical compound B12B3B4C32B41 INAHAJYZKVIDIZ-UHFFFAOYSA-N 0.000 description 1
- QUEICCDHEFTIQD-UHFFFAOYSA-N buta-1,3-diene;2-ethenylpyridine;styrene Chemical compound C=CC=C.C=CC1=CC=CC=C1.C=CC1=CC=CC=N1 QUEICCDHEFTIQD-UHFFFAOYSA-N 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 239000012933 diacyl peroxide Substances 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- FWDBOZPQNFPOLF-UHFFFAOYSA-N ethenyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)C=C FWDBOZPQNFPOLF-UHFFFAOYSA-N 0.000 description 1
- WOXXJEVNDJOOLV-UHFFFAOYSA-N ethenyl-tris(2-methoxyethoxy)silane Chemical compound COCCO[Si](OCCOC)(OCCOC)C=C WOXXJEVNDJOOLV-UHFFFAOYSA-N 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000009998 heat setting Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000004761 kevlar Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 229920000092 linear low density polyethylene Polymers 0.000 description 1
- 239000004707 linear low-density polyethylene Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- RXOHFPCZGPKIRD-UHFFFAOYSA-N naphthalene-2,6-dicarboxylic acid Chemical compound C1=C(C(O)=O)C=CC2=CC(C(=O)O)=CC=C21 RXOHFPCZGPKIRD-UHFFFAOYSA-N 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920002589 poly(vinylethylene) polymer Chemical class 0.000 description 1
- 238000012643 polycondensation polymerization Methods 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000010059 sulfur vulcanization Methods 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000004950 technora Substances 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- MTPVUVINMAGMJL-UHFFFAOYSA-N trimethyl(1,1,2,2,2-pentafluoroethyl)silane Chemical compound C[Si](C)(C)C(F)(F)C(F)(F)F MTPVUVINMAGMJL-UHFFFAOYSA-N 0.000 description 1
- UONOETXJSWQNOL-UHFFFAOYSA-N tungsten carbide Chemical compound [W+]#[C-] UONOETXJSWQNOL-UHFFFAOYSA-N 0.000 description 1
- 239000004762 twaron Substances 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は伝動ベルトに係り、
詳しくはVリブドベルト、カットエッジタイプのVベル
ト等の摩擦伝動タイプを含む動力伝動用ベルトであり、
プーリと接触する伝達面のベルト厚み方向の面租度を粗
く維持することできる層を積層することにより、伝達面
に水が付着しても高い伝動力を発揮することができ、ま
た高温雰囲気下及び低温雰囲気下でのベルト走行寿命が
向上し、耐候性にも優れる伝動ベルトに関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a power transmission belt,
Specifically, it is a power transmission belt including a friction transmission type such as a V-ribbed belt and a cut edge type V belt,
By laminating a layer that can roughly maintain the surface roughness of the transmission surface in contact with the pulley in the belt thickness direction, high power transmission can be achieved even if water adheres to the transmission surface. Also, the present invention relates to a power transmission belt having an improved belt running life in a low-temperature atmosphere and excellent weatherability.
【0002】[0002]
【従来の技術】近年、省エネルギー化、コンパクト化の
社会的要請を背景に、自動車のエンジンルーム周辺の雰
囲気温度は従来に比べて上昇してきている。これにとも
ないVリブドベルトの使用環境温度も高くなってきた。
従来、Vリブドベルトは主として天然ゴム、スチレン−
ブタジエンゴム、クロロプレンゴムが使用されてきた
が、高温雰囲気下では、硬化した圧縮ゴム層で早期にク
ラックを生じるという問題が発生した。このため、クロ
ロプレンゴムに代わってクロロスルフォン化ポリエチレ
ンゴムが使用されてきた。2. Description of the Related Art In recent years, due to social demands for energy saving and compactness, the ambient temperature around an engine room of an automobile has been increasing as compared with the related art. Along with this, the operating environment temperature of the V-ribbed belt has been increased.
Conventionally, V-ribbed belts are mainly made of natural rubber, styrene-
Butadiene rubber and chloroprene rubber have been used, but under a high-temperature atmosphere, there has been a problem that cracks occur early in the cured compressed rubber layer. For this reason, chlorosulfonated polyethylene rubber has been used instead of chloroprene rubber.
【0003】クロロスルフォン化ポリエチレンゴムを用
いたVリブドベルトは、クロロプレンゴムを用いたベル
トに比べると高温雰囲気下でのベルト走行寿命が大きく
向上し優れた耐熱性を有しているが、−30℃以下の低
温雰囲気下でのベルト走行寿命が著しく劣ることが明ら
かになった。この理由として、従来のクロロスルフォン
化ポリエチレンゴムは、ポリエチレンをクロロスルフォ
ン化したもので、塩素を含有しているため低温下では塩
素の凝集エネルギーが大きくなって低温領域でゴムの硬
化が起こってゴム弾性を欠き、割れ易くなるためと推定
される。A V-ribbed belt using chlorosulfonated polyethylene rubber has a significantly improved belt running life in a high-temperature atmosphere and excellent heat resistance as compared with a belt using chloroprene rubber. It became clear that the belt running life under the following low temperature atmosphere was remarkably inferior. The reason for this is that conventional chlorosulfonated polyethylene rubber is a chlorosulfonated polyethylene, which contains chlorine, so that the cohesive energy of chlorine increases at low temperatures and the rubber hardens in the low temperature range, causing the rubber to harden. This is presumed to be due to lack of elasticity and easy cracking.
【0004】これに対して、エチレン−プロピレン系ゴ
ム(EPR)あるいはエチレン−プロピレン−ジエン系
ゴム(EPDM)等のエチレン−α−オレフィンエラス
トマーは、優れた耐熱性、耐寒性を有し、比較的に安価
なポリマーであるが、耐油性を有していないため、油が
かかる用途には積極的に使用されていない。Vリブドベ
ルトのような乾式の摩擦伝動では多量の油がかかるとス
リップし、伝達機能が損なわれることより従来からあま
り使用されていなかったが、最近では例えば特開平6−
345948号公報に開示されているように、エチレン
−α−オレフィンエラストマーの使用した伝動ベルトも
検討されつつある。On the other hand, ethylene-α-olefin elastomers such as ethylene-propylene rubber (EPR) and ethylene-propylene-diene rubber (EPDM) have excellent heat resistance and cold resistance, and Although it is an inexpensive polymer, it does not have oil resistance, so it is not actively used for such applications. In dry friction transmission such as a V-ribbed belt, slippage occurs when a large amount of oil is applied, and the transmission function is impaired.
As disclosed in JP-A-345948, a transmission belt using an ethylene-α-olefin elastomer is also being studied.
【0005】また、上記Vリブドベルトも回転変動の大
きな条件や高負荷条件になると、圧縮ゴム層が粘着摩耗
を起こし、その結果粘着ゴムがリブ間の溝底に付着して
スリップ率が大きくなって所期の伝達馬力が得られなく
なったり、過度に粘着ゴムが付着すると、圧縮ゴム層が
剥離する問題があった。このために圧縮ゴム層に綿、ナ
イロン、ポリエステル等の短繊維の量を多くしたり、カ
ーボンブラックなどを増量していた。また、圧縮ゴム層
にセラッミクス粉を混入して、粘着摩耗に対処してい
た。Also, when the V-ribbed belt is subjected to a condition of large rotation fluctuation or a high load condition, the compressed rubber layer causes adhesive wear, and as a result, the adhesive rubber adheres to the groove bottom between the ribs to increase the slip ratio. If the desired transmission horsepower cannot be obtained or the adhesive rubber is excessively adhered, there has been a problem that the compressed rubber layer peels off. For this reason, the amount of short fibers such as cotton, nylon and polyester has been increased in the compressed rubber layer, and the amount of carbon black and the like has been increased. In addition, ceramics powder was mixed into the compressed rubber layer to cope with adhesive wear.
【0006】[0006]
【発明が解決しようとする課題】しかし、圧縮ゴム層に
短繊維、カーボンブラックなどを増量したり、セラッミ
クス粉を均一に混入すると、ベルト幅方向のモジュラス
が高くなって、ベルト長手方向の伸びが減少することに
なった。その結果、Vリブドベルトは耐屈曲性の低下が
生じ、特に逆曲げ走行において早期に圧縮ゴム層に亀裂
が発生した。また、リブ面に水が付着した場合には、摩
擦係数の低下が起こり、スリップしやすくなって伝達能
力が低下することがあった。However, if short fibers, carbon black, etc. are added to the compressed rubber layer, or if ceramics powder is uniformly mixed, the modulus in the belt width direction increases, and the elongation in the belt longitudinal direction increases. Will be reduced. As a result, the bending resistance of the V-ribbed belt deteriorated, and cracks occurred in the compression rubber layer at an early stage particularly during reverse bending. In addition, when water adheres to the rib surface, the friction coefficient is reduced, slipping is likely to occur, and the transmission capacity may be reduced.
【0007】本発明はこのような問題に対処するもので
あり、プーリと接触する伝達面のベルト厚み方向の面租
度を粗く維持することできる層を積層することにより、
伝達面に水が付着しても高い伝動力を発揮することがで
き、また高温雰囲気下及び低温雰囲気下でのベルト走行
寿命が向上し、耐候性にも優れる伝動ベルトを提供する
ことを目的とする。The present invention addresses such a problem, and by stacking layers capable of roughly maintaining the roughness of the transmission surface in contact with the pulley in the belt thickness direction,
An object of the present invention is to provide a power transmission belt that can exhibit high power transmission even if water adheres to the transmission surface, has an improved belt running life under high-temperature atmosphere and low-temperature atmosphere, and has excellent weather resistance. I do.
【0008】[0008]
【課題を解決するための手段】即ち、本願の請求項1の
発明では、表面にカバー帆布を積層し、ベルト長手方向
に沿って心線を埋設した接着ゴム層に隣接して圧縮ゴム
層を配置した伝動ベルトにおいて、上記圧縮ゴム層では
ゴム中に無機質材料微粒子を分散した少なくとも1層の
微粒子分散ゴム層がゴム中に短繊維を分散した短繊維混
入ゴム層に介在している伝動ベルトにあり、微粒子分散
ゴム層が表面の面租度を粗く、長時間維持することによ
って伝達面に水が付着しても高い伝動力を発揮すること
ができ、また微粒子分散ゴム層が圧縮ゴム層中に局部的
に介在することによって、ベルト幅方向のモジュラスも
高くならず、ベルト長手方向の伸びも維持され、耐屈曲
性が阻害されることがない。That is, in the invention of claim 1 of the present application, a cover canvas is laminated on the surface, and a compressed rubber layer is formed adjacent to an adhesive rubber layer in which a cord is embedded along the longitudinal direction of the belt. In the transmission belt arranged, in the compression rubber layer, at least one fine particle dispersion rubber layer in which inorganic material fine particles are dispersed in rubber is interposed in a short fiber mixed rubber layer in which short fibers are dispersed in rubber. Yes, the fine particle-dispersed rubber layer has a rough surface roughness and can maintain high power even if water adheres to the transmission surface by maintaining it for a long time. Locally, the modulus in the belt width direction does not increase, the elongation in the belt longitudinal direction is maintained, and the bending resistance is not hindered.
【0009】本願の請求項2の発明では、微粒子分散ゴ
ム層の無機質材料微粒子がセラミックス粉である伝動ベ
ルトにある。According to a second aspect of the present invention, there is provided a power transmission belt in which the inorganic material fine particles of the fine particle dispersed rubber layer are ceramic powder.
【0010】本願の請求項3の発明では、微粒子分散ゴ
ム層の無機質材料微粒子が珪藻土である伝動ベルトにあ
る。According to a third aspect of the present invention, there is provided a power transmission belt in which the fine particles of the inorganic material in the fine particle dispersed rubber layer are diatomaceous earth.
【0011】本願の請求項4の発明では、圧縮ゴム層の
ゴムが有機過酸化物で架橋させたエチレン−α−オレフ
ィンエラストマーの架橋物である伝動ベルトにある。According to a fourth aspect of the present invention, there is provided a power transmission belt in which the rubber of the compressed rubber layer is a crosslinked product of an ethylene-α-olefin elastomer crosslinked with an organic peroxide.
【0012】本願の請求項5の発明では、伝動ベルトが
ベルト長手方向に沿って心線を埋設した接着ゴムと、ベ
ルトの周方向に延びる複数のリブ部をもつ圧縮ゴム層か
らなるVリブドベルトである。According to the invention of claim 5 of the present application, the transmission belt is a V-ribbed belt composed of an adhesive rubber having a core buried along the belt longitudinal direction and a compression rubber layer having a plurality of rib portions extending in the circumferential direction of the belt. is there.
【0013】[0013]
【発明の実施の形態】図1に示すVリブドベルト1は、
ポリエステル繊維、アラミド繊維、ガラス繊維を素材と
する高強度で低伸度のコードよりなる心線2を接着ゴム
層3中に埋設し、その下側に弾性体層である圧縮ゴム層
4を有している。この圧縮ゴム層4にはベルト長手方向
にのびる断面略三角形の複数のリブ部7が設けられ、ま
たベルト表面には付着したカバー帆布5が設けられてい
る。DESCRIPTION OF THE PREFERRED EMBODIMENTS A V-ribbed belt 1 shown in FIG.
A core wire 2 made of a high-strength, low-elongation cord made of polyester fiber, aramid fiber, or glass fiber is embedded in an adhesive rubber layer 3, and a compression rubber layer 4 as an elastic layer is provided below the core wire. are doing. The compressed rubber layer 4 is provided with a plurality of ribs 7 having a substantially triangular cross section extending in the longitudinal direction of the belt, and a cover canvas 5 attached to the surface of the belt.
【0014】他のベルトとしてカットエッジタイプのV
ベルト21にも使用される。このベルト21は、図2に
示すように心線23を埋設した接着ゴム層24と圧縮ゴ
ム26とから構成され、更に上記接着ゴム層24及び圧
縮ゴム層26の各表面層にカバー帆布22を積層してい
る。As another belt, a cut edge type V
Also used for the belt 21. As shown in FIG. 2, the belt 21 is composed of an adhesive rubber layer 24 in which a cord 23 is embedded and a compressed rubber 26, and a cover canvas 22 is further provided on each surface layer of the adhesive rubber layer 24 and the compressed rubber layer 26. Laminated.
【0015】しかして、図1及び図2に示す圧縮ゴム層
4、26では、ゴム中に無機質材料の微粒子を分散した
一層の微粒子分散ゴム層8、28がゴム中に短繊維を分
散した短繊維混入ゴム層9、29中に介在している。こ
の微粒子分散ゴム層8、28の厚みは0.15〜1.0
mmであり、0.15mm未満の場合には、該ゴム層の
作製が困難なばかりか、伝達面の面租度を粗くすること
が困難になり、他方1.0mmを超えると、ベルト長手
方向のモジュラスが高くなるだけでなく、ベルト長手方
向の伸びも低下するので、耐屈曲性が阻害される。Thus, in the compressed rubber layers 4 and 26 shown in FIGS. 1 and 2, one layer of fine particle-dispersed rubber layers 8 and 28 in which fine particles of an inorganic material are dispersed in rubber has a short fiber in which short fibers are dispersed in rubber. It is interposed in the fiber-containing rubber layers 9 and 29. The thickness of the fine particle dispersed rubber layers 8 and 28 is 0.15 to 1.0.
mm and less than 0.15 mm, it is difficult not only to manufacture the rubber layer but also to make the surface roughness of the transmission surface rough, while if it exceeds 1.0 mm, the belt lengthwise Not only does the modulus of elasticity increase, but also the elongation in the belt longitudinal direction decreases, so that the bending resistance is impaired.
【0016】微粒子分散ゴム層8、28の無機質材料微
粒子は、001〜100μmの炭化珪素、炭化チタン、
炭化ホウ素、炭化タングステン等の炭化物、窒化珪素、
窒化アルミニウム、窒化ホウ素、窒化チタン等の窒化
物、アルミナ、ジルコニア、ベベリア等の酸化物であ
り、最も好ましくは炭化珪素や窒化珪素である。また、
珪藻土等の多孔質材も使用することができる。上記無機
質材料微粒子の添加量はゴム100重量部に対して5〜
40重量部であり、5重量部未満の場合には、ベルト厚
み方向の面粗度を粗くすることの効果がなく、一方40
重量部を超えると、加工性が悪化するだけでなく耐久性
が低下し、これ以上添加してもベルト厚み方向の面粗度
は変わらない。The inorganic material fine particles of the fine particle dispersed rubber layers 8 and 28 are made of 001 to 100 μm silicon carbide, titanium carbide,
Carbides such as boron carbide and tungsten carbide, silicon nitride,
Nitride such as aluminum nitride, boron nitride, and titanium nitride; and oxides such as alumina, zirconia, and bevelia, and most preferably, silicon carbide and silicon nitride. Also,
A porous material such as diatomaceous earth can also be used. The addition amount of the inorganic material fine particles is 5 to 100 parts by weight of rubber.
If it is less than 5 parts by weight, there is no effect of increasing the surface roughness in the belt thickness direction.
When the amount is more than the weight part, not only the workability is deteriorated but also the durability is lowered, and even if added more, the surface roughness in the belt thickness direction does not change.
【0017】前記圧縮ゴム層4、26に使用されるゴム
としては、エチレン−α−オレフィンエラストマーとと
もにニトリルゴム、水素化ニトリルゴム、水素化ニトリ
ルゴムに不飽和カルボン酸金属塩を添加したもの、クロ
ロスルフォン化ポリエチレン、クロロプレン、ウレタン
ゴム、エピクロルヒドリンゴム、天然ゴム、CSM、A
CSM、SBRが使用される。このうち、エチレン−α
−オレフィンエラストマーが好まし。The rubber used for the compressed rubber layers 4 and 26 includes nitrile rubber, hydrogenated nitrile rubber, hydrogenated nitrile rubber to which unsaturated carboxylic acid metal salt is added together with ethylene-α-olefin elastomer, Sulfonated polyethylene, chloroprene, urethane rubber, epichlorohydrin rubber, natural rubber, CSM, A
CSM and SBR are used. Among them, ethylene-α
-Olefin elastomers are preferred.
【0018】このエチレン−α−オレフィンエラストマ
ーはエチレン−プロピレンゴム(EPR)やエチレン−
プロピレン−ジエンモノマー(EPDM)からなるゴム
をいう。ジエンモノマーの例としては、ジシクロペンタ
ジエン、メチレンノルボルネン、エチリデンノルボルネ
ン、1,4−ヘキサジエン、シクロオクタジエンなどが
あげられる。The ethylene-α-olefin elastomer is ethylene-propylene rubber (EPR) or ethylene-propylene rubber.
A rubber composed of a propylene-diene monomer (EPDM). Examples of diene monomers include dicyclopentadiene, methylene norbornene, ethylidene norbornene, 1,4-hexadiene, cyclooctadiene, and the like.
【0019】上記圧縮ゴム層4、26には、エチレン−
α−オレフィンエラストマーの加硫剤としてパーオキサ
イドを添加する。また、共架橋剤(co−agent)
としTIAC、TAC、1,2ポリブタジエン、不飽和
カルボン酸の金属塩、オキシム類、グアニジン、トリメ
チロールプロパントリメタクリレート、エチレングリコ
ールジメタクリレート、N−N’−m−フェニレンビス
マレイミド、硫黄など通常パーオキサイド架橋に用いる
ものである。The compressed rubber layers 4 and 26 have ethylene-
A peroxide is added as a vulcanizing agent for the α-olefin elastomer. Also, a co-crosslinking agent (co-agent)
Normal peroxides such as TIAC, TAC, 1,2 polybutadiene, metal salts of unsaturated carboxylic acids, oximes, guanidine, trimethylolpropane trimethacrylate, ethylene glycol dimethacrylate, N-N'-m-phenylenebismaleimide, and sulfur It is used for crosslinking.
【0020】この中でもN,N’−m−フェニレンジマ
レイミドが好ましく、これを添加することによって架橋
度を上げて粘着摩耗等を防止することができる。N,
N’−m−フェニレンジマレイミドの添加量はエチレン
−α−オレフィンエラストマー100重量部に対して
0.2〜10重量部であり、0.2重量部未満の場合に
は、架橋密度が小さくなり耐摩耗性、耐粘着摩耗性の改
善効果が小さく、一方10重量部を越えると加硫ゴムの
伸びの低下が著しく、耐屈曲性に問題が生じる。更に、
上記圧縮ゴム層4、26には、硫黄をエチレン−α−オ
レフィンエラストマー100重量部に対して0.01〜
1重量部添加することにより、加硫ゴムの伸びの低下を
制御することができる。1重量部を越えると、架橋度が
期待できる程に向上しないため、加硫ゴムの未耐摩耗
性、耐粘着摩耗性も向上しなくなる。Of these, N, N'-m-phenylenedimaleimide is preferred, and the addition of N, N'-m-phenylenedimaleimide increases the degree of cross-linking and can prevent adhesive abrasion and the like. N,
The addition amount of N'-m-phenylenedimaleimide is 0.2 to 10 parts by weight with respect to 100 parts by weight of the ethylene-α-olefin elastomer. The effect of improving the abrasion resistance and the adhesive abrasion resistance is small. On the other hand, if it exceeds 10 parts by weight, the elongation of the vulcanized rubber is remarkably reduced, causing a problem in the bending resistance. Furthermore,
The compressed rubber layers 4 and 26 contain sulfur in an amount of 0.01 to 100 parts by weight based on the ethylene-α-olefin elastomer.
By adding 1 part by weight, a decrease in elongation of the vulcanized rubber can be controlled. If the amount exceeds 1 part by weight, the degree of crosslinking does not improve as expected, so that the non-wear resistance and adhesive wear resistance of the vulcanized rubber also do not improve.
【0021】上記有機過酸化物としては、通常、ゴム、
樹脂の架橋に使用されているジアシルパーオキサイド、
パーオキシエステル、ジアリルパーオキサイド、ジ−t
−ブチルパーオキサイド、t−ブチルクミルパーオキサ
イド、ジクミルパーオキサイド、2・5−ジメチル−2
・5−ジ(t−ブチルパーオキシ)−ヘキサン−3,1
・3−ビス(t−ブチルパーオキシ−イソプロピル)ベ
ンゼン、1・1−ジ−ブチルパーオキシ−3,3,5−
トリメチルシクロヘキサン等があり、熱分解による1分
間の半減期が150〜250°Cのものが好ましい。As the above-mentioned organic peroxide, usually, rubber,
Diacyl peroxide used for crosslinking of resin,
Peroxyester, diallyl peroxide, di-t
-Butyl peroxide, t-butylcumyl peroxide, dicumyl peroxide, 2.5-dimethyl-2
.5-di (t-butylperoxy) -hexane-3,1
• 3-bis (t-butylperoxy-isopropyl) benzene, 1,1-di-butylperoxy-3,3,5-
Trimethylcyclohexane and the like, and those having a one-minute half-life by thermal decomposition of 150 to 250 ° C. are preferable.
【0022】その添加量はエチレン−α−オレフィンエ
ラストマー100重量部に対して約1〜8重量部であ
り、好ましくは1.5〜4重量部である。The addition amount is about 1 to 8 parts by weight, preferably 1.5 to 4 parts by weight, based on 100 parts by weight of the ethylene-α-olefin elastomer.
【0023】また、圧縮ゴム層4、26には、ナイロン
6、ナイロン66、ポリエステル、綿、アラミドからな
る短繊維を混入して圧縮ゴム層4の耐側圧性を向上させ
るとともに、プーリと接する面になる圧縮ゴム層4の表
面をグラインダーによって研磨加工して該短繊維を突出
させる。圧縮ゴム層4の表面の摩擦係数は低下して、ベ
ルト走行時の騒音を軽減する。これらの短繊維のうち、
剛直で強度を有し、しかも耐磨耗性を有するアラミド短
繊維が最も効果がある。Short fibers made of nylon 6, nylon 66, polyester, cotton, and aramid are mixed in the compressed rubber layers 4 and 26 to improve the lateral pressure resistance of the compressed rubber layer 4 and to make contact with the pulley. The surface of the compressed rubber layer 4 is polished by a grinder to project the short fibers. The coefficient of friction of the surface of the compressed rubber layer 4 is reduced, and noise during belt running is reduced. Of these short fibers,
Aramid short fibers, which are rigid and strong and have abrasion resistance, are most effective.
【0024】上記アラミド短繊維が前述の効果を充分に
発揮するためには、アラミド繊維の繊維長さは1〜20
mmで、その添加量はエチレン−α−オレフィンエラス
トマー100重量部に対して1〜30重量部である。こ
のアラミド繊維は分子構造中に芳香環をもつアラミド、
例えば商品名コーネックス、ノーネックス、ケブラー、
テクノーラ、トワロン等である。In order for the aramid short fibers to sufficiently exhibit the above-mentioned effects, the fiber length of the aramid fibers should be 1 to 20.
mm, the amount is 1 to 30 parts by weight based on 100 parts by weight of the ethylene-α-olefin elastomer. This aramid fiber has an aramid having an aromatic ring in the molecular structure,
For example, brand names Conex, Nonex, Kevlar,
Technora, Twaron, etc.
【0025】また、圧縮ゴム層4、26には、マトリク
スゴムであるエチレン−α−オレフィンエラストマー1
00重量部に対して、エチレン−α−オレフィンエラス
トマーと繊維径1.0μm以下、好ましくは0.05〜
0.8μmの微小短繊維とをグラフト結合した微小短繊
維強化ゴムを繊維分で1〜50重量部、好ましくは5〜
25重量部含有してもよい。上記微小短繊維強化ゴムの
配合量が1重量部未満では耐摩耗性が充分でなく、また
50重量部を越えるとゴム組成物の伸びが低下し、耐熱
性、耐屈曲性が低下する。The compressed rubber layers 4 and 26 have an ethylene-α-olefin elastomer 1 as a matrix rubber.
With respect to 00 parts by weight, an ethylene-α-olefin elastomer and a fiber diameter of 1.0 μm or less, preferably 0.05 to
1 to 50 parts by weight, preferably 5 to 5 parts by weight of a micro-short fiber reinforced rubber graft-bonded with 0.8 μm micro-short fibers
25 parts by weight may be contained. If the blending amount of the short microfiber reinforced rubber is less than 1 part by weight, abrasion resistance is not sufficient, and if it exceeds 50 parts by weight, elongation of the rubber composition is reduced, and heat resistance and bending resistance are reduced.
【0026】この微小短繊維強化ゴムは、これを構成し
ているエチレン−α−オレフィンエラストマーが圧縮ゴ
ム層4、26のマトリクスゴムのエチレン−α−オレフ
ィンエラストマーと全く同質かもしくは類似しているた
め、マトリクスゴムと良好に接合する。このため、微小
短繊維強化ゴムとマトリクスゴムとの間、あるいは微小
短繊維強化ゴム中でもエチレン−α−オレフィンエラス
トマーと微小短繊維とが化学結合しているため、圧縮ゴ
ム層4、26では亀裂が入りにくく、たとえ亀裂が発生
しても伝播しにくい。In the micro-short fiber reinforced rubber, the ethylene-α-olefin elastomer constituting it is completely the same or similar to the ethylene-α-olefin elastomer of the matrix rubber of the compressed rubber layers 4 and 26. Good bonding with matrix rubber. For this reason, since the ethylene-α-olefin elastomer and the short microfiber are chemically bonded between the short microfiber reinforced rubber and the matrix rubber, or even in the short microfiber reinforced rubber, cracks are formed in the compressed rubber layers 4 and 26. Difficult to penetrate, even if cracks occur.
【0027】前記微小短繊維強化ゴムにおいて、この微
小短繊維とエチレン−α−オレフィンエラストマーとの
界面はカップリング剤、例えばビニルトリス(β−メト
キシエトキシ)シラン、ビニルトリエトキシシラン、γ
−メタクリロキシプロピルトリメトキシシラン等のシラ
ンカップリング剤、イソプロピルトリイソステアロイル
チタネートを始めとするチタネート系カップリング剤、
アクリル酸、メタアクリル酸、マレイン酸等の不飽和カ
ルボン酸、あるいはノボラック型フェノール樹脂等の接
着剤を介してグラフトしているものであり、エチレン−
α−オレフィンエラストマーと微小短繊維、そしてカッ
プリング剤等の接着剤を上記短繊維が溶融する温度以上
で混練し押出して得たものである。[0027] In the above short fiber reinforced rubber, the interface between the short fibers and the ethylene-α-olefin elastomer is a coupling agent such as vinyl tris (β-methoxyethoxy) silane, vinyl triethoxy silane, γ.
-Silane coupling agents such as methacryloxypropyltrimethoxysilane, titanate coupling agents including isopropyl triisostearoyl titanate,
Acrylic acid, methacrylic acid, unsaturated carboxylic acid such as maleic acid, or grafted via an adhesive such as novolak type phenol resin, ethylene-
It is obtained by kneading and extruding an adhesive such as an α-olefin elastomer, micro short fibers, and a coupling agent at a temperature at which the short fibers melt.
【0028】この微小短繊維強化ゴムはゴム成分を連続
相とし、その中に微小短繊維が微細な形態で分散し、微
小短繊維はその界面でゴム成分と強固な化学結合、ある
いは相互作用している。このため、これを含んだゴム層
には亀裂が入りにくく、しかも亀裂が入っても伝播しに
くい。しかも、これを使用したベルトも耐熱性、耐寒
性、耐屈曲性、耐摩耗性に優れる。The short microfiber reinforced rubber has a rubber component as a continuous phase in which the short microfibers are dispersed in a fine form, and the short microfibers form a strong chemical bond or interaction with the rubber component at the interface. ing. For this reason, the rubber layer containing this hardly cracks, and even if the cracks do not easily propagate. Moreover, the belt using this also has excellent heat resistance, cold resistance, bending resistance, and abrasion resistance.
【0029】更に、圧縮ゴム層4、26には、必要に応
じてカーボンブラック、シリカなどの補強剤、クレー、
炭酸カルシウムなどの充填剤、軟化剤、加工助剤、老化
防止剤、TAICなどの共架橋剤などの各種薬剤を添加
してもよい。The compressed rubber layers 4 and 26 may further include a reinforcing agent such as carbon black and silica, clay,
Various agents such as a filler such as calcium carbonate, a softener, a processing aid, an antioxidant, and a co-crosslinking agent such as TAIC may be added.
【0030】また、上記圧縮ゴム層4、26には、エチ
レン−α−オレフィンエラストマーとともにニトリルゴ
ム、水素化ニトリルゴム、水素化ニトリルゴムに不飽和
カルボン酸金属塩を添加したもの、クロロスルフォン化
ポリエチレン、クロロプレン、ウレタンゴム、エピクロ
ルヒドリンゴム、天然ゴム、CSM、ACSM、SBR
が使用される。The above-mentioned compressed rubber layers 4 and 26 are made of nitrile rubber, hydrogenated nitrile rubber, hydrogenated nitrile rubber to which an unsaturated carboxylic acid metal salt is added together with ethylene-α-olefin elastomer, chlorosulfonated polyethylene. , Chloroprene, urethane rubber, epichlorohydrin rubber, natural rubber, CSM, ACSM, SBR
Is used.
【0031】水素化ニトリルゴムは水素添加率80%以
上で、耐熱性及び耐オゾン性の特性を発揮するために、
好ましくは90%以上が良い。水素添加率80%未満の
水素化ニトリルゴムは、耐熱性及び耐オゾン性は極度に
低下する。耐油性及び耐寒性を考慮すると、結合アクリ
ロニトリル量は20〜45%の範囲が好ましい。The hydrogenated nitrile rubber has a hydrogenation rate of 80% or more, and exhibits heat resistance and ozone resistance characteristics.
Preferably, 90% or more is good. A hydrogenated nitrile rubber having a hydrogenation rate of less than 80% has extremely low heat resistance and ozone resistance. In consideration of oil resistance and cold resistance, the amount of bound acrylonitrile is preferably in the range of 20 to 45%.
【0032】クロロスルフォン化ポリエチレンは塩素含
有量15〜35重量%、好ましくは25〜32重量%
で、かつ硫黄含有量が0.5〜2.5重量%の範囲にな
るようにクロロスルフォン化した直鎖状低密度ポリエチ
レンである。The chlorosulfonated polyethylene has a chlorine content of 15 to 35% by weight, preferably 25 to 32% by weight.
And a chlorosulfonated linear low-density polyethylene having a sulfur content in the range of 0.5 to 2.5% by weight.
【0033】前記接着ゴム層3、24にも圧縮ゴム層
4、26と同様のエチレン−α−オレフィンエラストマ
ー組成物が使用される。しかし、心線であるポリエステ
ル繊維、アラミド繊維、ガラス繊維等と良好に接着する
ために、パーオキサイドを含まない硫黄加硫によるエチ
レン−α−オレフィンエラストマー組成物や、クロロス
ルフォン化ポリエチレン組成物もしくは水素化ニトリル
ゴム組成物を使用することもできる。For the adhesive rubber layers 3 and 24, the same ethylene-α-olefin elastomer composition as that for the compressed rubber layers 4 and 26 is used. However, in order to adhere well to the polyester fiber, aramid fiber, glass fiber, etc., which is the core wire, an ethylene-α-olefin elastomer composition by sulfur vulcanization containing no peroxide, a chlorosulfonated polyethylene composition or hydrogen Nitrile rubber compositions can also be used.
【0034】心線2、23にはポリエチレンテレフタレ
ート繊維、エチレン−2,6−ナフタレートを主たる構
成単位とするポリエステル繊維、ポリアミド繊維からな
るロープが使用され、ゴムとの接着性を改善する目的で
接着処理が施される。このような接着処理としては繊維
をレゾルシン−ホルマリン−ラテックス(RFL液)に
浸漬後、加熱乾燥して表面に均一に接着層を形成するの
が一般的である。しかし、これに限ることなくエポキシ
又はイソシアネート化合物で前処理を行なった後に、R
FL液で処理する方法等もある。For the cords 2 and 23, ropes made of polyethylene terephthalate fiber, polyester fiber having ethylene-2,6-naphthalate as a main constituent unit, and polyamide fiber are used, and are bonded for the purpose of improving adhesion to rubber. Processing is performed. As such an adhesive treatment, it is common to immerse the fiber in resorcin-formalin-latex (RFL solution) and then heat and dry to form an adhesive layer uniformly on the surface. However, without being limited to this, after pretreatment with an epoxy or isocyanate compound, R
There is also a method of treating with an FL solution.
【0035】本発明で使用するエチレン−2,6−ナフ
タレートは、通常ナフタレン−2,6−ジカルボン酸ま
たはそのエステル形成性誘導体を触媒の存在下に適当な
条件のもとにエチレングリコールと縮重合させることに
よって合成させる。このとき、エチレン−2,6−ナフ
タレートの重合完結前に適当な1種または2種以上の第
3成分を添加すれば、共重合体ポリエステルが合成され
る。The ethylene-2,6-naphthalate used in the present invention is usually prepared by condensation polymerization of naphthalene-2,6-dicarboxylic acid or an ester-forming derivative thereof with ethylene glycol in the presence of a catalyst under appropriate conditions. To be synthesized. At this time, if one or more appropriate third components are added before the completion of the polymerization of ethylene-2,6-naphthalate, a copolymer polyester is synthesized.
【0036】上記心線の接着処理は、まず(1)未処理
コードをエポキシ化合物やイソシアネート化合物から選
ばれた処理液を入れたタンクに含浸してプレディップし
た後、(2)160〜200°Cに温度設定した乾燥炉
に30〜600秒間通して乾燥し、(3)続いてRFL
液からなる接着液を入れたタンクに浸漬し、(4)21
0〜260°Cに温度設定した延伸熱固定処理機に30
〜600秒間通して−1〜3%延伸して延伸処理コード
とする。First, the unbonded cord is impregnated into a tank containing a treatment liquid selected from an epoxy compound and an isocyanate compound and pre-dip, and then (2) 160 to 200 °. C through a drying oven set at a temperature of 30 to 600 seconds for drying.
(4) 21
30 to the stretching heat setting processor set at a temperature of 0 to 260 ° C.
Stretching is performed for 1〜31 to 3% for 600600 seconds to obtain a stretched cord.
【0037】RFL液はレゾルシンとホルマリンとの初
期縮合体をラテックスに混合したものであり、ここで使
用するラテックスとしてはクロロプレン、スチレン・ブ
タジエン・ビニルピリジン三元共重合体、水素化ニトリ
ル、NBR等である。The RFL solution is prepared by mixing a latex with an initial condensate of resorcinol and formalin, and the latex used herein includes chloroprene, styrene / butadiene / vinylpyridine terpolymer, hydrogenated nitrile, NBR, etc. It is.
【0038】上記カバー帆布5、22は、綿、ポリアミ
ド、ポリエチレンテレフタレート、アラミド繊維からな
る糸を用いて、平織、綾織、朱子織等に製織した布をR
FL処理にて接着処理してスピニング工程で筒状のベル
ト帆布のしわ発生を阻止する。RFL処理はRFL液に
0.1〜20秒間浸漬した後、100〜200℃で30
〜600秒にて乾燥させ、オーバーロックなどのミシン
がけ縫製により少なくとも1つのジョイント部を有する
筒状帆布にする。尚、RFL液には適宜カーボンブラッ
ク液を混合して処理反を黒染めする場合もある。綿織物
の場合には、RFL液に公知の界面活性剤を0.1〜
1.0重量%加えるとよい。The cover canvases 5 and 22 are made of a cloth woven in a plain weave, a twill weave, a satin weave, or the like using a thread made of cotton, polyamide, polyethylene terephthalate, or aramid fiber.
Adhesion treatment is performed by FL treatment to prevent wrinkling of the tubular belt canvas in the spinning process. The RFL treatment is performed by immersing in the RFL solution for 0.1 to 20 seconds and then at 100 to 200 ° C. for 30 minutes.
After drying for about 600 seconds, a tubular canvas having at least one joint is formed by sewing with an overlock or the like. In some cases, a carbon black liquid is appropriately mixed with the RFL liquid to blacken the treated material. In the case of cotton fabric, a known surfactant is added to the RFL solution in an amount of 0.1 to 0.1%.
It is advisable to add 1.0% by weight.
【0039】Vリブドベルト1の製造方法の一例は以下
の通りである。まず、円筒状の成形ドラムの周面に1〜
複数枚のカバー帆布とクッションゴム層とを巻き付けた
後、この上にロープからなる心線を螺旋状にスピニング
し、更に圧縮ゴム層を順次巻き付けて積層体を得た後、
これを加硫して加硫スリーブを得る。An example of a method for manufacturing the V-ribbed belt 1 is as follows. First, on the peripheral surface of the cylindrical forming drum,
After winding a plurality of cover canvases and a cushion rubber layer, a cord made of a rope is spirally spun on this, and a compressed rubber layer is sequentially wound thereon to obtain a laminate,
This is vulcanized to obtain a vulcanized sleeve.
【0040】次に、加硫スリーブを駆動ロールと従動ロ
ールに掛架され所定の張力下で走行させ、更に回転させ
た研削ホイールを走行中の加硫スリーブに当接するよう
に移動して加硫スリーブの圧縮ゴム層表面に3〜100
個の複数の溝状部を一度に研削する。Next, the vulcanization sleeve is hung between a driving roll and a driven roll and travels under a predetermined tension, and the rotated grinding wheel is moved so as to abut the traveling vulcanization sleeve to perform vulcanization. 3 to 100 on the surface of the compression rubber layer of the sleeve
The plurality of groove portions are ground at one time.
【0041】このようにして得られた加硫スリーブを駆
動ロールと従動ロールから取り外し、該加硫スリーブを
他の駆動ロールと従動ロールに掛架して走行させ、カッ
ターによって所定に幅に切断して個々のVリブドベルト
に仕上げる。The vulcanization sleeve obtained in this manner is removed from the driving roll and the driven roll, and the vulcanization sleeve is hung on another driving roll and the driven roll to travel, and cut into a predetermined width by a cutter. To make individual V-ribbed belts.
【0042】[0042]
【実施例】以下、本発明を実施例により更に詳細に説明
する。The present invention will be described in more detail with reference to the following examples.
【0043】実施例1、比較例1 本実施例で製造したVリブドベルトでは、ポリエステル
繊維のロープからなる心線を接着ゴム層内に埋設し、そ
の上側にRFL液(スチレン−ブタジエン−ビニルピリ
ジン三元共重合体100重量部、レゾルシン14.6重
量部、ホルマリン9.2重量部、苛性ソーダ1.5重量
部、水262.5重量部)のみで処理した綿帆布を1プ
ライ積層し、他方接着ゴム層の下側には圧縮ゴム層があ
って3個のリブをベルト長手方向に有している。得られ
たVリブドベルトはRMA規格による長さ975mmの
K型3リブドベルトであり、リブピッチ3.56mm、
リブ高さ2.0mm、ベルト厚さ4.3mm、リブ角度
40°である。Example 1 and Comparative Example 1 In the V-ribbed belt manufactured in this example, a core wire made of a polyester fiber rope was embedded in an adhesive rubber layer, and an RFL solution (styrene-butadiene-vinylpyridine triethyl) was placed on the upper side thereof. 1 ply of cotton canvas treated only with 100 parts by weight of the original copolymer, 14.6 parts by weight of resorcinol, 9.2 parts by weight of formalin, 1.5 parts by weight of caustic soda, and 262.5 parts by weight of water A compressed rubber layer is provided below the rubber layer and has three ribs in the longitudinal direction of the belt. The obtained V-ribbed belt is a K-type 3-ribbed belt having a length of 975 mm according to the RMA standard and a rib pitch of 3.56 mm.
The rib height is 2.0 mm, the belt thickness is 4.3 mm, and the rib angle is 40 °.
【0044】ここで圧縮ゴム層を、それぞれ表1に示す
短繊維混入ゴム層と微粒子分散ゴム層の2種のゴム組成
物から調製し、バンバリーミキサーで混練後、カレンダ
ーロールで圧延したものを用いた。圧縮ゴム層には短繊
維が含まれベルト幅方向に配向している。尚、実施例1
の圧縮ゴム層では、3mmの短繊維混入ゴム層を短繊維
混入ゴム層中に1層設け、他方比較例2では短繊維混入
ゴム層のみとしたものである。Here, a compressed rubber layer was prepared from two types of rubber compositions, a short fiber mixed rubber layer and a fine particle dispersed rubber layer shown in Table 1, kneaded with a Banbury mixer, and then rolled with calender rolls. Was. The compressed rubber layer contains short fibers and is oriented in the belt width direction. Example 1
In the compressed rubber layer, one rubber layer mixed with short fibers having a length of 3 mm is provided in the rubber layer mixed with short fibers, while in Comparative Example 2, only the rubber layer mixed with short fibers is used.
【0045】[0045]
【表1】 [Table 1]
【0046】ベルトの製造方法は通常の方法であり、ま
ず平滑な円筒モールドに1プライのミシンジョイントし
たRFL液でのみ処理した綿製の筒状のカバー帆布を挿
入した後、接着ゴム層を巻き付けて、心線をスピニング
し、更に圧縮ゴム層を配置した後、圧縮ゴム層の上に架
橋用ジャケットを挿入する。次いで、モールドを加硫缶
内に入れ、架橋した後、筒状の架橋スリーブをモールド
から取り出し、該スリーブの圧縮ゴム層をグラインダー
によってリブに成形し、成形体から個々のベルトに切断
する工程からなっている。The belt is manufactured in the usual manner. First, a cotton cylindrical cover canvas treated only with the RFL solution, which has been subjected to one ply sewing machine joint, is inserted into a smooth cylindrical mold, and then the adhesive rubber layer is wound thereon. After spinning the core wire and further arranging the compressed rubber layer, a crosslinking jacket is inserted on the compressed rubber layer. Next, the mold is placed in a vulcanizing can, and after crosslinking, the tubular cross-linked sleeve is removed from the mold, the compressed rubber layer of the sleeve is formed into ribs by a grinder, and the individual molded product is cut into individual belts. Has become.
【0047】このようにして得られたVリブドベルトの
注水走行試験による2%スリップ時のトルク、そしてベ
ルト厚み方向のリブ表面の粗さを測定した。この結果は
表2に示される。The V-ribbed belt thus obtained was subjected to a water injection running test to measure the torque at the time of 2% slip and the roughness of the rib surface in the belt thickness direction. The results are shown in Table 2.
【0048】注水走行試験は、駆動プーリ(直径120
mm)、従動プーリ(直径120mm)、これにテンシ
ョンプーリ(直径80mm)とを組み合わせて配置した
ものである。試験機の各プーリにベルトを掛架し、駆動
プーリの入り側に注水量10cc/秒で注水しながら室
温、駆動プーリの回転数2000rpm、ベルト張力1
47N/3リブで200時間走行させた。In the water injection running test, a drive pulley (120 mm diameter) was used.
mm), a driven pulley (120 mm in diameter), and a tension pulley (80 mm in diameter) in combination. A belt is hung on each pulley of the tester, and water is injected into the entrance side of the driving pulley at a water injection rate of 10 cc / sec. At room temperature, the number of rotations of the driving pulley is 2000 rpm, and the belt tension is 1
The vehicle was run for 200 hours on a 47N / 3 rib.
【0049】[0049]
【表2】 [Table 2]
【0050】この結果から明らかなように、伝達面に水
が付着しても高い伝動力を発揮することができることが
判る。As is clear from these results, it is understood that high power transmission can be achieved even when water adheres to the transmission surface.
【0051】[0051]
【発明の効果】以上のように本願の請求項の発明では、
微粒子分散ゴム層が伝達面のベルト厚み方向の面租度を
粗く、長時間維持することによって伝達面に水が付着し
ても高い伝動力を発揮することができ、また微粒子分散
ゴム層が圧縮ゴム層中に局部的に介在することによっ
て、ベルト幅方向のモジュラスも高くならず、ベルト長
手方向の伸びも維持され、耐屈曲性が阻害されることが
ない。また、圧縮ゴム層にエチレン−アルファ−オレフ
ィンエラストマーを使用することで、高温雰囲気下及び
低温雰囲気下でのベルト走行寿命が向上し、耐候性にも
優れる効果がある。As described above, according to the present invention,
The fine particle-dispersed rubber layer has a rough surface roughness in the belt thickness direction of the transmission surface, and can maintain high power even if water adheres to the transmission surface by maintaining it for a long time. By intervening locally in the rubber layer, the modulus in the belt width direction does not increase, the elongation in the belt longitudinal direction is maintained, and the bending resistance is not hindered. In addition, by using an ethylene-alpha-olefin elastomer for the compressed rubber layer, the running life of the belt in a high-temperature atmosphere and a low-temperature atmosphere is improved, and the weather resistance is also excellent.
【図1】本発明に係るVリブドベルトの縦断面図であ
る。FIG. 1 is a longitudinal sectional view of a V-ribbed belt according to the present invention.
【図2】本発明に係るVカットエッジタイプのVベルト
の縦断面図である。FIG. 2 is a vertical sectional view of a V-cut edge type V-belt according to the present invention.
1 Vリブドベルト 2、23 心線 3、24 接着ゴム層 4、26 圧縮ゴム層 5、22 カバー帆布 7 リブ部 8、28 微粒子分散ゴム層 9、29 短繊維混入ゴム層 21 Vベルト Reference Signs List 1 V-ribbed belt 2, 23 core wire 3, 24 Adhesive rubber layer 4, 26 Compressed rubber layer 5, 22 Cover canvas 7 Rib portion 8, 28 Fine particle dispersed rubber layer 9, 29 Short fiber mixed rubber layer 21 V belt
Claims (5)
方向に沿って心線を埋設した接着ゴム層に隣接して圧縮
ゴム層を配置した伝動ベルトにおいて、上記圧縮ゴム層
ではゴム中に無機質材料微粒子を分散した少なくとも1
層の微粒子分散ゴム層がゴム中に短繊維を分散した短繊
維混入ゴム層に介在していることを特徴とする伝動ベル
ト。1. A power transmission belt in which a cover canvas is laminated on the surface and a compression rubber layer is disposed adjacent to an adhesive rubber layer in which a core wire is embedded along the longitudinal direction of the belt. At least one in which material fine particles are dispersed
A power transmission belt, wherein the fine particle-dispersed rubber layer is interposed in a short fiber-mixed rubber layer in which short fibers are dispersed in rubber.
セラミックス粉である請求項1記載の伝動ベルト。2. The power transmission belt according to claim 1, wherein the fine particles of the inorganic material in the fine particle dispersed rubber layer are ceramic powder.
珪藻土である請求項1記載の伝動ベルト。3. The power transmission belt according to claim 1, wherein the inorganic material fine particles of the fine particle dispersed rubber layer are diatomaceous earth.
させたエチレン−α−オレフィンエラストマーの架橋物
である請求項1記載の伝動ベルト。4. The power transmission belt according to claim 1, wherein the rubber of the compression rubber layer is a crosslinked product of an ethylene-α-olefin elastomer crosslinked with an organic peroxide.
線を埋設した接着ゴムと、ベルトの周方向に延びる複数
のリブ部をもつ圧縮ゴム層からなるVリブドベルトであ
る請求項1または2記載の伝動ベルト。5. The transmission belt according to claim 1, wherein the transmission belt is a V-ribbed belt comprising an adhesive rubber having a core buried along the longitudinal direction of the belt and a compression rubber layer having a plurality of rib portions extending in the circumferential direction of the belt. Transmission belt.
Priority Applications (1)
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JP33200299A JP4495285B2 (en) | 1999-11-22 | 1999-11-22 | Transmission belt |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2001146942A true JP2001146942A (en) | 2001-05-29 |
JP4495285B2 JP4495285B2 (en) | 2010-06-30 |
Family
ID=18250049
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JP33200299A Expired - Fee Related JP4495285B2 (en) | 1999-11-22 | 1999-11-22 | Transmission belt |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004162897A (en) * | 2002-07-30 | 2004-06-10 | Mitsuboshi Belting Ltd | V-ribbed belt and its manufacturing method |
JP2005098470A (en) * | 2002-10-17 | 2005-04-14 | Mitsuboshi Belting Ltd | Toothed belt |
EP1510726A3 (en) * | 2003-08-25 | 2005-06-29 | Bando Chemical Industries, Ltd. | Friction drive belt and method for fabricating the same |
WO2005078311A1 (en) * | 2004-02-13 | 2005-08-25 | Bando Chemical Industries, Ltd. | Transmission belt and process for producing the same |
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JPS59147944U (en) * | 1983-03-24 | 1984-10-03 | バンドー化学株式会社 | Multi-projection belt |
JPS6267351A (en) * | 1985-09-13 | 1987-03-27 | Mitsuboshi Belting Ltd | Wear resisting v belt |
JPH06249292A (en) * | 1992-12-29 | 1994-09-06 | Bridgestone Corp | Toothed belt |
-
1999
- 1999-11-22 JP JP33200299A patent/JP4495285B2/en not_active Expired - Fee Related
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
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JPS59147944U (en) * | 1983-03-24 | 1984-10-03 | バンドー化学株式会社 | Multi-projection belt |
JPS6267351A (en) * | 1985-09-13 | 1987-03-27 | Mitsuboshi Belting Ltd | Wear resisting v belt |
JPH06249292A (en) * | 1992-12-29 | 1994-09-06 | Bridgestone Corp | Toothed belt |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004162897A (en) * | 2002-07-30 | 2004-06-10 | Mitsuboshi Belting Ltd | V-ribbed belt and its manufacturing method |
JP2005098470A (en) * | 2002-10-17 | 2005-04-14 | Mitsuboshi Belting Ltd | Toothed belt |
EP1510726A3 (en) * | 2003-08-25 | 2005-06-29 | Bando Chemical Industries, Ltd. | Friction drive belt and method for fabricating the same |
WO2005078311A1 (en) * | 2004-02-13 | 2005-08-25 | Bando Chemical Industries, Ltd. | Transmission belt and process for producing the same |
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