USRE30137E - High-modulus rubber composition for pneumatic tires - Google Patents
High-modulus rubber composition for pneumatic tires Download PDFInfo
- Publication number
- USRE30137E USRE30137E US05/916,699 US91669978A USRE30137E US RE30137 E USRE30137 E US RE30137E US 91669978 A US91669978 A US 91669978A US RE30137 E USRE30137 E US RE30137E
- Authority
- US
- United States
- Prior art keywords
- tire
- composition
- sidewall
- cobalt
- rubber
- 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.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 30
- 229920001971 elastomer Polymers 0.000 title claims description 26
- 239000005060 rubber Substances 0.000 title claims description 24
- 244000043261 Hevea brasiliensis Species 0.000 claims abstract description 16
- 229920003052 natural elastomer Polymers 0.000 claims abstract description 16
- 229920001194 natural rubber Polymers 0.000 claims abstract description 16
- 239000003963 antioxidant agent Substances 0.000 claims abstract description 10
- 229910017052 cobalt Inorganic materials 0.000 claims abstract description 7
- 239000010941 cobalt Substances 0.000 claims abstract description 7
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims abstract description 7
- 230000003078 antioxidant effect Effects 0.000 claims abstract description 5
- 239000000344 soap Substances 0.000 claims abstract description 4
- 150000001869 cobalt compounds Chemical class 0.000 claims description 9
- 229920001195 polyisoprene Polymers 0.000 claims description 7
- AMFIJXSMYBKJQV-UHFFFAOYSA-L cobalt(2+);octadecanoate Chemical compound [Co+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O AMFIJXSMYBKJQV-UHFFFAOYSA-L 0.000 claims description 6
- 230000003014 reinforcing effect Effects 0.000 claims description 5
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- 229920001568 phenolic resin Polymers 0.000 claims description 4
- 239000005011 phenolic resin Substances 0.000 claims description 4
- 229920005989 resin Polymers 0.000 claims description 4
- 239000011347 resin Substances 0.000 claims description 4
- 239000006229 carbon black Substances 0.000 claims description 3
- KVBYPTUGEKVEIJ-UHFFFAOYSA-N benzene-1,3-diol;formaldehyde Chemical compound O=C.OC1=CC=CC(O)=C1 KVBYPTUGEKVEIJ-UHFFFAOYSA-N 0.000 claims description 2
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 2
- 239000000194 fatty acid Substances 0.000 claims description 2
- 229930195729 fatty acid Natural products 0.000 claims description 2
- 150000004665 fatty acids Chemical class 0.000 claims description 2
- 239000006232 furnace black Substances 0.000 claims description 2
- 238000009998 heat setting Methods 0.000 claims description 2
- 238000012545 processing Methods 0.000 claims description 2
- 150000004989 p-phenylenediamines Chemical class 0.000 claims 2
- 239000006235 reinforcing carbon black Substances 0.000 abstract description 3
- 230000009467 reduction Effects 0.000 abstract description 2
- 235000006708 antioxidants Nutrition 0.000 abstract 1
- 239000011324 bead Substances 0.000 description 9
- 239000000463 material Substances 0.000 description 8
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 4
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 230000006835 compression Effects 0.000 description 3
- 238000007906 compression Methods 0.000 description 3
- 238000010276 construction Methods 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 230000001066 destructive effect Effects 0.000 description 2
- 239000000806 elastomer Substances 0.000 description 2
- 239000004312 hexamethylene tetramine Substances 0.000 description 2
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 229960004011 methenamine Drugs 0.000 description 2
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 2
- 238000013021 overheating Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 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 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- 238000004073 vulcanization Methods 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- HLBZWYXLQJQBKU-UHFFFAOYSA-N 4-(morpholin-4-yldisulfanyl)morpholine Chemical compound C1COCCN1SSN1CCOCC1 HLBZWYXLQJQBKU-UHFFFAOYSA-N 0.000 description 1
- IGFAHOKFJJCIHD-UHFFFAOYSA-N 4-n-butyl-1-n,1-n-dimethyl-4-n-phenylbenzene-1,4-diamine Chemical compound C=1C=C(N(C)C)C=CC=1N(CCCC)C1=CC=CC=C1 IGFAHOKFJJCIHD-UHFFFAOYSA-N 0.000 description 1
- 239000006238 High Abrasion Furnace Substances 0.000 description 1
- UTGQNNCQYDRXCH-UHFFFAOYSA-N N,N'-diphenyl-1,4-phenylenediamine Chemical compound C=1C=C(NC=2C=CC=CC=2)C=CC=1NC1=CC=CC=C1 UTGQNNCQYDRXCH-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 230000032683 aging Effects 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
- 239000003054 catalyst Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000006231 channel black Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000013536 elastomeric material Substances 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- GZNRISJLOXVOSH-UHFFFAOYSA-N n-phenylaniline;propan-2-one Chemical compound CC(C)=O.C=1C=CC=CC=1NC1=CC=CC=C1 GZNRISJLOXVOSH-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 150000004986 phenylenediamines Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 238000010058 rubber compounding Methods 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 238000009988 textile finishing Methods 0.000 description 1
- 239000004636 vulcanized rubber Substances 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60C—VEHICLE TYRES; TYRE INFLATION; TYRE CHANGING; CONNECTING VALVES TO INFLATABLE ELASTIC BODIES IN GENERAL; DEVICES OR ARRANGEMENTS RELATED TO TYRES
- B60C1/00—Tyres characterised by the chemical composition or the physical arrangement or mixture of the composition
- B60C1/0025—Compositions of the sidewalls
-
- 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
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T152/00—Resilient tires and wheels
- Y10T152/10—Tires, resilient
- Y10T152/10495—Pneumatic tire or inner tube
- Y10T152/10855—Characterized by the carcass, carcass material, or physical arrangement of the carcass materials
- Y10T152/10864—Sidewall stiffening or reinforcing means other than main carcass plies or foldups thereof about beads
Definitions
- This invention is especially useful in the pneumatic tire of the application for patent of John T. Alden, Michael G. Miller, and Stephen C. Sabo Ser. No. 513,413 filed Oct. 9, 1974 and assigned to the same owner as this application.
- Pneumatic tires are subject to failure from loss of air because of punctures, blowouts, or spontaneous leaks and then generally collapse. As a consequence, they are then likely to be severely damaged by rim cutting, or chafing, or breakage of cords, so that they are unsuitable for further use. Many efforts have been made to protect tires against such damage by use of auxiliary devices to prevent collapse. Such devices are expensive, cumbersome, and generally not completely successful.
- the principal object of this invention accordingly, is to provide a rubber composition of permanently high modulus and low hysteresis for use in the sidewalls of tires designed for operation both with and without inflation air.
- a rubber composition for the sidewalls of tires intended for use on motor vehicles both with and without presence of inflation air.
- This composition is made essentially from natural rubber or from the synthetic cis-polyisoprene rubber, which is chemically identical with natural rubber, or from blends of such materials.
- the rubber is mixed with a substantial proportion of reinforcing carbon black and preferably also with a small proportion of a heat settable phenolic resin such as that produced by mixing resorcinol with hexamethylene tetramine.
- a heat settable phenolic resin such as that produced by mixing resorcinol with hexamethylene tetramine.
- it contains conventional vulcanizing agents and antioxidants or antiozonants.
- compositions containing the foregoing ingredients are well known and provide satisfactory initial properties after vulcanization.
- natural rubber after prolonged exposure to heat, undergoes reversion, which means that the initial stiff high-modulus vulcanized material gradually softens and exhibits lower and lower modulus values approaching that of the original unvulcanized crude rubber, which ultimately are too low for satisfactory support of the weight by an uninflated tire.
- Other elastomers are known which do not undergo reversion, such as the butadiene-styrene rubbers which are extensively used in making tires for passenger cars and other lightweight vehicles, but such synthetic rubber materials have such a high hysteresis that the intense flexure resulting from operation without inflation air can result in rapid overheating and consequent destruction of the tire.
- compositions which performs satisfactorily both when freshly vulcanized and after long service, maintaining its high modulus and low hysteresis without significant change can be made from natural rubber or its true synthetic duplicate containing the conventional materials mentioned above, together with a small proportion of a cobalt compound, preferably a cobalt soap, such as cobalt stearate.
- a cobalt compound preferably a cobalt soap, such as cobalt stearate.
- Cobalt compounds are well known as cross-linking promoters and are extensively used as paint driers and as catalysts for the setting of various kinds of synthetic resins. They have generally been rigorously avoided in rubber compounding because of their known ability to induce rapid oxidation and consequent early failure of rubber.
- composition of this invention may be used in the sidewalls of any pneumatic tire of the type in which the weight of the vehicle is borne entirely on the sidewalls without collapse of the tread against the rim, but it is particularly intended to be used in making the type of tire described in the copending application mentioned above.
- a specific tire of this kind is illustrated in cross section in the accompanying drawing, in which the tire 5 consists of a tread 6 and a pair of sidewalls 7 and 8 extending from the tread 6 to the annular beads 9 and 10.
- the tire 5 is reinforced by a conventional nearly inextensible textile or metal cord ply 11 which may have the individual cords located in radial planes.
- the cord ply 11 extends from bead 9 to bead 10 and as is usual is folded around the beads and outward into the sidewall rubber.
- a belt structure 12 is placed between the crown portion 13 of the cord ply 11 and the tread rubber 6.
- the belt is of any conventional construction which is essentially inextensible circumferentially and provides adequate lateral stiffness, such as a combination of steel cord plies and textile cord plies at opposite small angles to the midplane of the tire, under the entire width of the tread.
- the main reinforcing ply 11 is embedded throughout in rubber so that there is a layer of rubber inside the ply 11 and another layer of rubber outside of the ply 11.
- the tire differs from conventional pneumatic tires in having sidewalls of substantially increased thickness, approaching or even equalling the thickness of the tread.
- the reinforcing ply 11 is not uniformly distant from the surfaces as is usual.
- the cord ply 11 near the beads 9 and 10 is quite close to the inner surface 14, which in a tubeless tire is the air-retaining liner layer.
- the outer surface opposite the beads 9 and 10 is only thick enough to embed the part of ply 11 which is wrapped around the bead and any textile finishing strip which might or might not be present.
- the sidewall immediately beyond the tip of the rim flange 16 is greatly thickened on the outside and contoured to rest against the tip of rim flange 16. This is in the zone of the sidewall marked 1st in the drawing.
- the retention of the initial high modulus is equally important since it minimizes the extent of the cyclic compression and relaxation under a given load and therefore plays an auxiliary role in minimizing heat generation.
- the new tire sidewall composition of this invention may be prepared from 100 parts by weight of true natural rubber or the synthetic duplicate of natural rubber, together with about 35 to 50 parts of reinforcing carbon black, and conventional vulcanizing agents, such as 1.5 parts sulfur, 2 parts dithio dimorpholine, 1.5 parts cyclohexyl benzothiazyl sulfenamide, and 10 parts zinc oxide.
- the composition must also contain highly active antioxidants or antiozonants, such as 0.25 parts diphenyl p-phenylene diamine, 0.7 parts diphenylamine-acetone reaction product, and 2 parts dimethyl butylphenyl p-phenylene diamine.
- heat setting resin such as phenolic resin which most advantageously is a resorcinol formaldehyde resin such as is produced by incorporation of 2.5 parts resorcinol and 1.6 parts hexamethylene tetramine, which functions as a formaldehyde donor.
- phenolic resin which most advantageously is a resorcinol formaldehyde resin such as is produced by incorporation of 2.5 parts resorcinol and 1.6 parts hexamethylene tetramine, which functions as a formaldehyde donor.
- cobalt stearate or an equivalent active cobalt compound such as cobalt naphthenate.
- a suitable elastomer base may be a natural rubber blend of ribbed smoked sheets with brown blankets, plasticated, and then further mixed with one-half its weight of synthetic cis-polyisoprene of 75 to 90 Mooney viscosity. Unless qualified, "cis-polyisoprene" is used to designate both natural rubber and its synthetic equivalent.
- the carbon black may be any of the reinforcing blacks such as channel black or high abrasion furnace black, but best results are presently obtained with a moderately high proportion of a high-modulus black, such as 40 parts of superior processing furnace black which produces a desirably high modulus without undue increase in hysteresis.
- vulcanizing materials give excellent results, but a great many other materials are available and may be substituted if the compounder has had good experience in using them to produce vulcanized products of stable physical properties.
- sulfur or sulfur-donors are presently preferred for vulcanization, with a sulfenamide type accelerator and a fairly high proportion of zinc oxide.
- Softeners such as oils, fusible resins, and fatty acids should be avoided as far as possible since they tend to offset or detract from the essential high modulus of the rubber sidewall compositions.
- the combination of highly active antioxidants with a cobalt compound is important to success of the invention, since insufficient antioxidant could result in resinification of the rubber by the catalytic action of the cobalt, and insufficient cobalt could result in achievement of an inadequate balance between the normal reversion and the cross-linking induced by the cobalt.
- the highly active substituted phenylene diamine antioxidants or their equivalents not less than about 4 to 5 parts of cobalt stearate should be used and not more than about 8 parts.
- the solid cobalt stearate is preferred over other available active cobalt compounds such as liquid cobalt naphthenate, since the stearate is a solid and therefore has a minimum softening effect on the vulcanized rubber composition.
- composition as described above performs extremely well under normal service conditions as the sidewall material in the type of tire having a thick sidewall. Also, because of its peculiar combination of high modulus and low hysteresis, it performs very well without inflation air, if the sidewall is properly proportioned, permitting operation of such a tire for many miles at reasonably high speeds without production of destructive sharp folds, and without overheating.
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Tires In General (AREA)
Abstract
Description
Claims (10)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/916,699 USRE30137E (en) | 1974-10-09 | 1978-06-19 | High-modulus rubber composition for pneumatic tires |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/513,414 US3983919A (en) | 1974-10-09 | 1974-10-09 | High-modulus rubber composition for pneumatic tires |
| US05/916,699 USRE30137E (en) | 1974-10-09 | 1978-06-19 | High-modulus rubber composition for pneumatic tires |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US05/513,414 Reissue US3983919A (en) | 1974-10-09 | 1974-10-09 | High-modulus rubber composition for pneumatic tires |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USRE30137E true USRE30137E (en) | 1979-11-06 |
Family
ID=27057859
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US05/916,699 Expired - Lifetime USRE30137E (en) | 1974-10-09 | 1978-06-19 | High-modulus rubber composition for pneumatic tires |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | USRE30137E (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5464899A (en) * | 1992-12-30 | 1995-11-07 | Bridgestone Corporation | High modulus low hysteresis rubber compound for pneumatic tires |
| US6672351B1 (en) * | 1999-08-31 | 2004-01-06 | Dunlop Gmbh | Vehicle tire with continously reducing vertical spacing of tread surface with respect to breaker |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2582795A (en) * | 1949-12-27 | 1952-01-15 | Phillips Petroleum Co | Organo-cobalt chelates as accelerators of vulcanization |
| US2891926A (en) * | 1954-02-03 | 1959-06-23 | Us Rubber Co | Process for promoting the low-hysteresis processing of rubber and carbon black using an aryl polyhalogenomethane |
| US3514370A (en) * | 1965-10-04 | 1970-05-26 | Pirelli | Zinc laminate and method for bonding unsaturated amorphous olefine copolymers by adding cobalt salt or organic carboxylic acid to promote adhesion |
| US3903026A (en) * | 1972-12-21 | 1975-09-02 | Bridgestone Tire Co Ltd | Rubber composition for adhering zinc or zinc alloy plated steel |
| US4076668A (en) * | 1976-02-27 | 1978-02-28 | The Yokohama Rubber Co., Ltd. | Rubber composition |
-
1978
- 1978-06-19 US US05/916,699 patent/USRE30137E/en not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2582795A (en) * | 1949-12-27 | 1952-01-15 | Phillips Petroleum Co | Organo-cobalt chelates as accelerators of vulcanization |
| US2891926A (en) * | 1954-02-03 | 1959-06-23 | Us Rubber Co | Process for promoting the low-hysteresis processing of rubber and carbon black using an aryl polyhalogenomethane |
| US3514370A (en) * | 1965-10-04 | 1970-05-26 | Pirelli | Zinc laminate and method for bonding unsaturated amorphous olefine copolymers by adding cobalt salt or organic carboxylic acid to promote adhesion |
| US3903026A (en) * | 1972-12-21 | 1975-09-02 | Bridgestone Tire Co Ltd | Rubber composition for adhering zinc or zinc alloy plated steel |
| US4076668A (en) * | 1976-02-27 | 1978-02-28 | The Yokohama Rubber Co., Ltd. | Rubber composition |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5464899A (en) * | 1992-12-30 | 1995-11-07 | Bridgestone Corporation | High modulus low hysteresis rubber compound for pneumatic tires |
| US5494958A (en) * | 1992-12-30 | 1996-02-27 | Bridgestone Corporation | High modulus low hysteresis rubber compound for pneumatic tires |
| US5494091A (en) * | 1992-12-30 | 1996-02-27 | Bridgestone Corporation | High modulus low hysteresis rubber compound for pneumatic tires |
| US6672351B1 (en) * | 1999-08-31 | 2004-01-06 | Dunlop Gmbh | Vehicle tire with continously reducing vertical spacing of tread surface with respect to breaker |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: UNIROYAL GOODRICH TIRE COMPANY, THE, 600 SOUTH MAI Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:B.F. GOODRICH COMPANY, THE;REEL/FRAME:004618/0798 Effective date: 19860801 |
|
| AS | Assignment |
Owner name: FIRST NATIONAL BANK OF CHICAGO, THE Free format text: SECURITY INTEREST;ASSIGNOR:UNIROYAL GOODRICH TIRE COMPANY, THE;REEL/FRAME:005004/0169 Effective date: 19880623 |
|
| AS | Assignment |
Owner name: UGTC, INC., 600 SOUTH MAIN STREET, AKRON, OH 44397 Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:UNIROYAL GOODRICH TIRE COMPANY, THE;REEL/FRAME:005617/0501 Effective date: 19901031 |
|
| AS | Assignment |
Owner name: UNIROYAL GOODRICH TIRE COMPANY, THE Free format text: CHANGE OF NAME;ASSIGNOR:UGTC, INC.;REEL/FRAME:006002/0042 Effective date: 19901101 |
|
| AS | Assignment |
Owner name: MICHELIN FINANCE (PAYS-BAS) Free format text: SECURITY INTEREST;ASSIGNOR:FIRST NATIONAL BANK OF CHICAGO, THE;REEL/FRAME:006169/0591 Effective date: 19911209 |
|
| AS | Assignment |
Owner name: UNIROYAL GOODRICH TIRE COMPANY, THE, OHIO Free format text: PARTIAL RELEASE;ASSIGNOR:MICHELIN FINANCE (PAYS-BAS) B.V.;REEL/FRAME:006401/0055 Effective date: 19911231 |
|
| AS | Assignment |
Owner name: UNIROYAL GOODRICH INTELLECTUAL PROPERTY, INC., DEL Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:UNIROYAL GOODRICH TIRE COMPANY, THE;REEL/FRAME:006539/0805 Effective date: 19911231 |
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| AS | Assignment |
Owner name: UNIROYAL GOODRICH LICENSING SERVICES, INC., DELAWA Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:UNIROYAL GOODRICH INTELLECTUAL PROPERTY, INC.;REEL/FRAME:006674/0487 Effective date: 19920102 |