JPS5953568A - ゴム組成物 - Google Patents
ゴム組成物Info
- Publication number
- JPS5953568A JPS5953568A JP58145142A JP14514283A JPS5953568A JP S5953568 A JPS5953568 A JP S5953568A JP 58145142 A JP58145142 A JP 58145142A JP 14514283 A JP14514283 A JP 14514283A JP S5953568 A JPS5953568 A JP S5953568A
- Authority
- JP
- Japan
- Prior art keywords
- rubber
- fixing agent
- parts
- adhesion
- agent according
- 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
- 229920001971 elastomer Polymers 0.000 title claims description 38
- 239000005060 rubber Substances 0.000 title claims description 38
- 229920000877 Melamine resin Polymers 0.000 title claims description 15
- 239000002184 metal Substances 0.000 title claims description 15
- 229910052751 metal Inorganic materials 0.000 title claims description 15
- 239000004640 Melamine resin Substances 0.000 title 1
- JYIZNFVTKLARKT-UHFFFAOYSA-N phenol;1,3,5-triazine-2,4,6-triamine Chemical compound OC1=CC=CC=C1.NC1=NC(N)=NC(N)=N1 JYIZNFVTKLARKT-UHFFFAOYSA-N 0.000 title 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 27
- 239000000203 mixture Substances 0.000 claims description 27
- 239000003795 chemical substances by application Substances 0.000 claims description 20
- 238000006243 chemical reaction Methods 0.000 claims description 14
- 238000010058 rubber compounding Methods 0.000 claims description 13
- 150000007974 melamines Chemical class 0.000 claims description 12
- 239000002318 adhesion promoter Substances 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- 239000007795 chemical reaction product Substances 0.000 claims description 10
- 150000001875 compounds Chemical class 0.000 claims description 7
- 229910001369 Brass Inorganic materials 0.000 claims description 6
- 239000010951 brass Substances 0.000 claims description 6
- 230000032683 aging Effects 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 238000012360 testing method Methods 0.000 claims description 4
- 125000002015 acyclic group Chemical group 0.000 claims description 3
- 230000000391 smoking effect Effects 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 229910000906 Bronze Inorganic materials 0.000 claims 2
- 239000010974 bronze Substances 0.000 claims 2
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 claims 2
- CTRPRMNBTVRDFH-UHFFFAOYSA-N 2-n-methyl-1,3,5-triazine-2,4,6-triamine Chemical compound CNC1=NC(N)=NC(N)=N1 CTRPRMNBTVRDFH-UHFFFAOYSA-N 0.000 claims 1
- 239000000853 adhesive Substances 0.000 claims 1
- 230000001070 adhesive effect Effects 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- 229920005989 resin Polymers 0.000 description 38
- 239000011347 resin Substances 0.000 description 38
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 27
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 18
- 238000009472 formulation Methods 0.000 description 13
- 229960003742 phenol Drugs 0.000 description 13
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 10
- 238000000034 method Methods 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- YQUQWHNMBPIWGK-UHFFFAOYSA-N 4-isopropylphenol Chemical compound CC(C)C1=CC=C(O)C=C1 YQUQWHNMBPIWGK-UHFFFAOYSA-N 0.000 description 6
- 229910000831 Steel Inorganic materials 0.000 description 6
- 239000010959 steel Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 150000002989 phenols Chemical class 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 239000006227 byproduct Substances 0.000 description 4
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical group NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 235000011941 Tilia x europaea Nutrition 0.000 description 3
- 238000004807 desolvation Methods 0.000 description 3
- 239000004571 lime Substances 0.000 description 3
- 238000006386 neutralization reaction Methods 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 230000002787 reinforcement Effects 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- 238000004073 vulcanization Methods 0.000 description 3
- GHMKDZIUDKBFIR-UHFFFAOYSA-N 4-(5-methyl-2-propan-2-ylcyclohexyl)phenol Chemical compound CC(C)C1CCC(C)CC1C1=CC=C(O)C=C1 GHMKDZIUDKBFIR-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-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
- 239000004594 Masterbatch (MB) Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000000370 acceptor Substances 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 125000006165 cyclic alkyl group Chemical group 0.000 description 2
- 239000000539 dimer Substances 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
- VLJSLTNSFSOYQR-UHFFFAOYSA-N meta-isopropyl phenol Natural products CC(C)C1=CC=CC(O)=C1 VLJSLTNSFSOYQR-UHFFFAOYSA-N 0.000 description 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 2
- 230000003472 neutralizing effect Effects 0.000 description 2
- KJIFKLIQANRMOU-UHFFFAOYSA-N oxidanium;4-methylbenzenesulfonate Chemical compound O.CC1=CC=C(S(O)(=O)=O)C=C1 KJIFKLIQANRMOU-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- 150000005207 1,3-dihydroxybenzenes Chemical class 0.000 description 1
- ZVJYNDILACLBLH-UHFFFAOYSA-N 2-(5-methyl-2-propan-2-ylcyclohexyl)phenol Chemical compound CC(C)C1CCC(C)CC1C1=CC=CC=C1O ZVJYNDILACLBLH-UHFFFAOYSA-N 0.000 description 1
- BNCADMBVWNPPIZ-UHFFFAOYSA-N 2-n,2-n,4-n,4-n,6-n,6-n-hexakis(methoxymethyl)-1,3,5-triazine-2,4,6-triamine Chemical compound COCN(COC)C1=NC(N(COC)COC)=NC(N(COC)COC)=N1 BNCADMBVWNPPIZ-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-ONCXSQPRSA-N abietic acid Chemical compound C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C(O)=O RSWGJHLUYNHPMX-ONCXSQPRSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- -1 alkyl phenol Chemical class 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000007767 bonding agent Substances 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
- 229920005549 butyl rubber Polymers 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 235000010216 calcium carbonate Nutrition 0.000 description 1
- 229920003211 cis-1,4-polyisoprene Polymers 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 230000001934 delay Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002085 enols Chemical class 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 150000005204 hydroxybenzenes Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 229940087305 limonene Drugs 0.000 description 1
- 235000001510 limonene Nutrition 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 238000006384 oligomerization reaction Methods 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- QAZLUNIWYYOJPC-UHFFFAOYSA-M sulfenamide Chemical compound [Cl-].COC1=C(C)C=[N+]2C3=NC4=CC=C(OC)C=C4N3SCC2=C1C QAZLUNIWYYOJPC-UHFFFAOYSA-M 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 238000005829 trimerization reaction Methods 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G14/00—Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00
- C08G14/02—Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes
- C08G14/04—Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes with phenols
- C08G14/06—Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes with phenols and monomers containing hydrogen attached to nitrogen
- C08G14/10—Melamines
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/04—Reinforcing macromolecular compounds with loose or coherent fibrous material
- C08J5/10—Reinforcing macromolecular compounds with loose or coherent fibrous material characterised by the additives used in the polymer mixture
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/35—Heterocyclic compounds having nitrogen in the ring having also oxygen in the ring
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2321/00—Characterised by the use of unspecified rubbers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Phenolic Resins Or Amino Resins (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US409790 | 1982-08-20 | ||
| US06/409,790 US4436853A (en) | 1982-08-20 | 1982-08-20 | Phenol-melamine resins for improving rubber to metal adhesion |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5953568A true JPS5953568A (ja) | 1984-03-28 |
| JPH0227375B2 JPH0227375B2 (en:Method) | 1990-06-15 |
Family
ID=23621982
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58145142A Granted JPS5953568A (ja) | 1982-08-20 | 1983-08-10 | ゴム組成物 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US4436853A (en:Method) |
| EP (1) | EP0104132B1 (en:Method) |
| JP (1) | JPS5953568A (en:Method) |
| CA (1) | CA1223693A (en:Method) |
| DE (1) | DE3366942D1 (en:Method) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6047750A (ja) * | 1983-08-17 | 1985-03-15 | ロ−ベルト・ボツシユ・ゲゼルシヤフト・ミツト・ベシユレンクテル・ハフツング | 自動車のブレ−キ装置 |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4785033A (en) * | 1984-02-27 | 1988-11-15 | The Goodyear Tire & Rubber Company | Rubber-metal adhesion promoters |
| US4578450A (en) * | 1984-09-04 | 1986-03-25 | The Goodyear Tire & Rubber Company | Accelerator-modified adhesion promoters for rubber to wire adhesion |
| US5723523A (en) * | 1996-05-22 | 1998-03-03 | Hankook Tire Mfg., Co., Ltd. | Rubber composition for a radial tire having improved processability and adhesive strength |
| US7132481B2 (en) * | 2002-05-17 | 2006-11-07 | The Goodyear Tire & Rubber Company | Composite of melamine derivative and carbon black, rubber composition and article having a component thereof |
| US7259199B2 (en) * | 2004-12-09 | 2007-08-21 | The Goodyear Tire & Rubber Company | Tire with rubber containing in-situ resin |
| US20060169382A1 (en) * | 2005-01-28 | 2006-08-03 | Sandstrom Paul H | Tire with internal cord reinforced rubber component |
| US7605202B2 (en) | 2007-11-27 | 2009-10-20 | The Goodyear Tire & Rubber Company | Tire with silica tread having self condensing resin |
| US20090151838A1 (en) * | 2007-12-17 | 2009-06-18 | Erik Paul Sandstrom | Tire containing an internal cord reinforced rubber component |
| KR101310180B1 (ko) | 2008-08-15 | 2013-09-23 | 오티스 엘리베이터 컴파니 | 코드 및 폴리머 재킷 재료 내에 접착 개량제를 갖는 폴리머 재킷 조립체 |
| US20100051157A1 (en) | 2008-08-29 | 2010-03-04 | Bina Patel Botts | Insert and belt overlay containing chopped carbon fibers |
| US8053510B2 (en) | 2009-09-03 | 2011-11-08 | The Goodyear Tire & Rubber Company | Pneumatic tire |
| US20110174422A1 (en) | 2010-01-20 | 2011-07-21 | Kelly Sue King | Pneumatic tire with compound apex |
| US8299165B2 (en) | 2011-02-24 | 2012-10-30 | The Goodyear Tire & Rubber Company | Pneumatic tire |
| US20120241066A1 (en) | 2011-03-24 | 2012-09-27 | Paul Harry Sandstrom | Tire containing an internal composite comprised of metal cord reinforced rubber layer with auxiliary buffer rubber layer |
| TWI418545B (zh) * | 2011-06-22 | 2013-12-11 | Taiwan Union Technology Corp | 三聚氰胺衍生物及其製法 |
| CN102408419B (zh) * | 2011-08-10 | 2014-11-05 | 哈尔滨理工大学 | 苯并噁嗪树脂的方法 |
| US20130133803A1 (en) | 2011-11-25 | 2013-05-30 | Paul Harry Sandstrom | Tire containing internal cord reinforced rubber layer |
| US9433971B2 (en) | 2012-10-04 | 2016-09-06 | The Goodyear Tire & Rubber Company | Atmospheric plasma treatment of reinforcement cords and use in rubber articles |
| US9441325B2 (en) | 2012-10-04 | 2016-09-13 | The Goodyear Tire & Rubber Company | Atmospheric plasma treatment of reinforcement cords and use in rubber articles |
| US8962719B2 (en) | 2012-11-01 | 2015-02-24 | The Goodyear Tire & Rubber Company | Rubber composition with encapsulated resin and pneumatic tire |
| US20140135433A1 (en) | 2012-11-13 | 2014-05-15 | The Goodyear Tire & Rubber Company | Tire with rubber containing flavone |
| EP2878458B1 (en) | 2013-11-27 | 2018-12-26 | The Goodyear Tire & Rubber Company | Pneumatic tire |
| US9387737B2 (en) | 2014-08-07 | 2016-07-12 | The Goodyear Tire & Rubber Company | Passage tube for air maintenance tire |
| US20160052344A1 (en) | 2014-08-20 | 2016-02-25 | The Goodyear Tire & Rubber Company | Rubber composition containing tin carboxylate salt |
| US20160167449A1 (en) | 2014-12-16 | 2016-06-16 | The Goodyear Tire & Rubber Company | Pneumatic tire |
| WO2016176080A1 (en) | 2015-04-30 | 2016-11-03 | Bridgestone Americas Tire Operations, Llc | Rubber-covered textile cords, tires containing same, and related methods |
| US10077342B2 (en) | 2016-01-21 | 2018-09-18 | Eastman Chemical Company | Elastomeric compositions comprising cellulose ester additives |
| US10427463B2 (en) | 2016-11-16 | 2019-10-01 | The Goodyear Tire & Rubber Company | Pneumatic tire having a dual layer tread |
| EP3336141B1 (en) | 2016-12-19 | 2019-08-14 | The Goodyear Tire & Rubber Company | Atmospheric plasma treatment of reinforcement cords and use in rubber articles |
| EP3336140B1 (en) | 2016-12-19 | 2019-07-24 | The Goodyear Tire & Rubber Company | Atmospheric plasma treatment of reinforcement cords and use in rubber articles |
| CN108570134B (zh) * | 2017-03-09 | 2020-12-29 | 北京彤程创展科技有限公司 | 一种烷基酚改性氨基树脂、制备方法及应用 |
| US20200070579A1 (en) | 2018-09-04 | 2020-03-05 | The Goodyear Tire & Rubber Company | Pneumatic tire |
| EP4015201B1 (en) | 2020-12-18 | 2023-09-13 | The Goodyear Tire & Rubber Company | Process for the production of a non-pneumatic tire |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5145146A (en:Method) * | 1974-08-09 | 1976-04-17 | American Cyanamid Co |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3293212A (en) | 1963-06-24 | 1966-12-20 | American Cyanamid Co | Thermosetting reaction product of hexakis-(alkoxymethyl) melamines and bisphenols |
| US3517722A (en) * | 1965-01-21 | 1970-06-30 | Goodyear Tire & Rubber | Wire cable-to-rubber adhesion |
| GB1119829A (en) | 1965-11-08 | 1968-07-17 | Ici Ltd | Adhesive compositions |
| US3904623A (en) | 1973-12-26 | 1975-09-09 | Sherwin Williams Co | Phenol-triazine addition products |
| DE2950940A1 (de) * | 1979-05-04 | 1980-11-06 | Gen Tire & Rubber Co | Reifencordklebstoffe |
| US4338263A (en) | 1979-05-04 | 1982-07-06 | The General Tire & Rubber Company | Tire cord adhesives |
-
1982
- 1982-08-20 US US06/409,790 patent/US4436853A/en not_active Expired - Lifetime
-
1983
- 1983-08-08 CA CA000434132A patent/CA1223693A/en not_active Expired
- 1983-08-10 JP JP58145142A patent/JPS5953568A/ja active Granted
- 1983-08-16 EP EP83630129A patent/EP0104132B1/en not_active Expired
- 1983-08-16 DE DE8383630129T patent/DE3366942D1/de not_active Expired
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5145146A (en:Method) * | 1974-08-09 | 1976-04-17 | American Cyanamid Co |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6047750A (ja) * | 1983-08-17 | 1985-03-15 | ロ−ベルト・ボツシユ・ゲゼルシヤフト・ミツト・ベシユレンクテル・ハフツング | 自動車のブレ−キ装置 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0227375B2 (en:Method) | 1990-06-15 |
| EP0104132B1 (en) | 1986-10-15 |
| US4436853A (en) | 1984-03-13 |
| DE3366942D1 (en) | 1986-11-20 |
| EP0104132A1 (en) | 1984-03-28 |
| CA1223693A (en) | 1987-06-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPS5953568A (ja) | ゴム組成物 | |
| EP3638652B1 (fr) | Benzoxazine sulfuree utilisable pour la synthese d'une polybenzoxazine | |
| JP4011484B2 (ja) | ゴム化合物用レゾルシノール誘導体 | |
| JP3413897B2 (ja) | 共縮合物およびそれを含有するゴム組成物 | |
| WO2018229416A1 (fr) | Polybenzoxazine sulfuree utilisable pour le revetement de metal et son collage a du caoutchouc | |
| DE2802984C2 (de) | Vulkanisierbare Kautschukmischungen und ihre Verwendung zum Verkleben von Kautschuk mit Verstärkermaterialien | |
| WO2018219882A1 (fr) | Benzoxazine borée utilisable pour la synthèse de polybenzoxazine | |
| WO2018215701A1 (fr) | Benzoxazine halogénée utilisable pour la synthèse de polybenzoxazine | |
| US3705911A (en) | Silyl-azidoformates | |
| WO2018229417A1 (fr) | Renfort metallique ou metallise dont la surface est revetue d'une polybenzoxazine sulfuree | |
| EP0798324A1 (fr) | Résines novolaques phenol/diene, procédé de préparation et compositions à base de caoutchouc renfermant lesdites résines | |
| EP0013402B1 (de) | Siloxanmodifizierte Novolake, deren Herstellung und Verwendung zur Herstellung von Reibbelägen | |
| JPH0439340A (ja) | ゴム組成物 | |
| CA1182615A (en) | Process for increasing the strength of the bond between rubber and metals | |
| JPS6041660A (ja) | 劣化防止剤 | |
| US4089902A (en) | Diallylaminomethyl-resorcinols | |
| JPS62201949A (ja) | ゴム組成物 | |
| US2970985A (en) | Curing catalysts for acrolein pentaerythritol resins | |
| CA1259615A (en) | Accelerator-modified adhesion promoters for rubber to wire adhesion | |
| JP4283906B2 (ja) | スチール製コードの接着性および加硫ゴムブレンドの剛性を向上させるためのウレタン変性ノボラックよりなる添加剤 | |
| JP4283906B6 (ja) | スチール製コードの接着性および加硫ゴムブレンドの剛性を向上させるためのウレタン変性ノボラックよりなる添加剤 | |
| JPH01249819A (ja) | ３，５―キシレノール・レゾルシン・ホルムアルデヒド縮合樹脂組成物からなる接着剤とその製造方法 | |
| EP0042478A1 (en) | Method for the adhesion of rubber to reinforcing materials | |
| JPS63314287A (ja) | 金属接着用ゴム組成物 | |
| PL38405B1 (en:Method) |