WO2018022876A1 - Carbamate resin for polyurethane adhesion - Google Patents
Carbamate resin for polyurethane adhesion Download PDFInfo
- Publication number
- WO2018022876A1 WO2018022876A1 PCT/US2017/044162 US2017044162W WO2018022876A1 WO 2018022876 A1 WO2018022876 A1 WO 2018022876A1 US 2017044162 W US2017044162 W US 2017044162W WO 2018022876 A1 WO2018022876 A1 WO 2018022876A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- rubber
- composite
- polyurethane
- adhesion
- rubber layer
- Prior art date
Links
- 229920002635 polyurethane Polymers 0.000 title claims abstract description 81
- 239000004814 polyurethane Substances 0.000 title claims abstract description 81
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 title description 4
- 239000011347 resin Substances 0.000 title description 3
- 229920005989 resin Polymers 0.000 title description 3
- 229920001971 elastomer Polymers 0.000 claims abstract description 131
- 239000005060 rubber Substances 0.000 claims abstract description 128
- 239000000203 mixture Substances 0.000 claims abstract description 124
- 239000002131 composite material Substances 0.000 claims abstract description 40
- 239000000758 substrate Substances 0.000 claims abstract description 34
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 36
- -1 alkyl urethane Chemical compound 0.000 claims description 23
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 22
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims description 16
- 239000012763 reinforcing filler Substances 0.000 claims description 15
- 239000006229 carbon black Substances 0.000 claims description 13
- 239000000377 silicon dioxide Substances 0.000 claims description 11
- BQBKYSPXQYHTIP-UHFFFAOYSA-N ethyl n-butylcarbamate Chemical compound CCCCNC(=O)OCC BQBKYSPXQYHTIP-UHFFFAOYSA-N 0.000 claims description 9
- 244000043261 Hevea brasiliensis Species 0.000 claims description 8
- 229920003052 natural elastomer Polymers 0.000 claims description 8
- 229920001194 natural rubber Polymers 0.000 claims description 8
- 229920002857 polybutadiene Polymers 0.000 claims description 6
- 230000001737 promoting effect Effects 0.000 claims description 6
- 229920003048 styrene butadiene rubber Polymers 0.000 claims description 5
- 229920001195 polyisoprene Polymers 0.000 claims description 4
- 239000010410 layer Substances 0.000 abstract description 37
- 239000012790 adhesive layer Substances 0.000 abstract description 2
- 238000010276 construction Methods 0.000 abstract description 2
- 150000001875 compounds Chemical class 0.000 description 22
- 239000000853 adhesive Substances 0.000 description 14
- 230000001070 adhesive effect Effects 0.000 description 14
- 238000000034 method Methods 0.000 description 11
- 150000002009 diols Chemical class 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 4
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 125000005442 diisocyanate group Chemical group 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 239000005062 Polybutadiene Substances 0.000 description 3
- SKKTUOZKZKCGTB-UHFFFAOYSA-N butyl carbamate Chemical compound CCCCOC(N)=O SKKTUOZKZKCGTB-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000000806 elastomer Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000002174 Styrene-butadiene Substances 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 235000006708 antioxidants Nutrition 0.000 description 2
- 229920001400 block copolymer Polymers 0.000 description 2
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229920006285 olefinic elastomer Polymers 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 239000011115 styrene butadiene Substances 0.000 description 2
- 229920003051 synthetic elastomer Polymers 0.000 description 2
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical class CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 2
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 1
- MTZUIIAIAKMWLI-UHFFFAOYSA-N 1,2-diisocyanatobenzene Chemical class O=C=NC1=CC=CC=C1N=C=O MTZUIIAIAKMWLI-UHFFFAOYSA-N 0.000 description 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
- 229940035437 1,3-propanediol Drugs 0.000 description 1
- OVBFMUAFNIIQAL-UHFFFAOYSA-N 1,4-diisocyanatobutane Chemical class O=C=NCCCCN=C=O OVBFMUAFNIIQAL-UHFFFAOYSA-N 0.000 description 1
- JIABEENURMZTTI-UHFFFAOYSA-N 1-isocyanato-2-[(2-isocyanatophenyl)methyl]benzene Chemical class O=C=NC1=CC=CC=C1CC1=CC=CC=C1N=C=O JIABEENURMZTTI-UHFFFAOYSA-N 0.000 description 1
- DXIJHCSGLOHNES-UHFFFAOYSA-N 3,3-dimethylbut-1-enylbenzene Chemical compound CC(C)(C)C=CC1=CC=CC=C1 DXIJHCSGLOHNES-UHFFFAOYSA-N 0.000 description 1
- 229920002943 EPDM rubber Polymers 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- HDEAYPRXFHBTAS-UHFFFAOYSA-N N=C=O.N=C=O.CC(C)C1=CC=CC=C1 Chemical class N=C=O.N=C=O.CC(C)C1=CC=CC=C1 HDEAYPRXFHBTAS-UHFFFAOYSA-N 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- 229920012485 Plasticized Polyvinyl chloride Polymers 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 description 1
- 125000000068 chlorophenyl group Chemical group 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 229920003244 diene elastomer Polymers 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 229920001973 fluoroelastomer Polymers 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical class O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 229920002681 hypalon Polymers 0.000 description 1
- 230000009878 intermolecular interaction Effects 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- YNTOKMNHRPSGFU-UHFFFAOYSA-N n-Propyl carbamate Chemical compound CCCOC(N)=O YNTOKMNHRPSGFU-UHFFFAOYSA-N 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
- 239000003921 oil Substances 0.000 description 1
- MYDQAEQZZKVJSL-UHFFFAOYSA-N pentyl carbamate Chemical compound CCCCCOC(N)=O MYDQAEQZZKVJSL-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001610 polycaprolactone Polymers 0.000 description 1
- 239000004632 polycaprolactone Substances 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 229920003225 polyurethane elastomer Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000037452 priming Effects 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000008096 xylene Substances 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B25/00—Layered products comprising a layer of natural or synthetic rubber
- B32B25/02—Layered products comprising a layer of natural or synthetic rubber with fibres or particles being present as additives in the layer
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B25/00—Layered products comprising a layer of natural or synthetic rubber
- B32B25/04—Layered products comprising a layer of natural or synthetic rubber comprising rubber as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B25/08—Layered products comprising a layer of natural or synthetic rubber comprising rubber as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B25/00—Layered products comprising a layer of natural or synthetic rubber
- B32B25/12—Layered products comprising a layer of natural or synthetic rubber comprising natural rubber
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B25/00—Layered products comprising a layer of natural or synthetic rubber
- B32B25/14—Layered products comprising a layer of natural or synthetic rubber comprising synthetic rubber copolymers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B25/00—Layered products comprising a layer of natural or synthetic rubber
- B32B25/16—Layered products comprising a layer of natural or synthetic rubber comprising polydienes homopolymers or poly-halodienes homopolymers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B25/00—Layered products comprising a layer of natural or synthetic rubber
- B32B25/18—Layered products comprising a layer of natural or synthetic rubber comprising butyl or halobutyl rubber
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/34—Layered products comprising a layer of synthetic resin comprising polyamides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/40—Layered products comprising a layer of synthetic resin comprising polyurethanes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B3/00—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form
- B32B3/26—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form characterised by a particular shape of the outline of the cross-section of a continuous layer; characterised by a layer with cavities or internal voids ; characterised by an apertured layer
- B32B3/30—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form characterised by a particular shape of the outline of the cross-section of a continuous layer; characterised by a layer with cavities or internal voids ; characterised by an apertured layer characterised by a layer formed with recesses or projections, e.g. hollows, grooves, protuberances, ribs
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/04—Interconnection of layers
- B32B7/10—Interconnection of layers at least one layer having inter-reactive properties
-
- 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
- B29D30/00—Producing pneumatic or solid tyres or parts thereof
- B29D30/06—Pneumatic tyres or parts thereof (e.g. produced by casting, moulding, compression moulding, injection moulding, centrifugal casting)
- B29D30/52—Unvulcanised treads, e.g. on used tyres; Retreading
- B29D30/54—Retreading
- B29D2030/547—Retreading solid tyres
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2250/00—Layers arrangement
- B32B2250/02—2 layers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2250/00—Layers arrangement
- B32B2250/24—All layers being polymeric
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2264/00—Composition or properties of particles which form a particulate layer or are present as additives
- B32B2264/10—Inorganic particles
- B32B2264/102—Oxide or hydroxide
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2264/00—Composition or properties of particles which form a particulate layer or are present as additives
- B32B2264/10—Inorganic particles
- B32B2264/107—Ceramic
- B32B2264/108—Carbon, e.g. graphite particles
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2270/00—Resin or rubber layer containing a blend of at least two different polymers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/70—Other properties
- B32B2307/748—Releasability
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2605/00—Vehicles
-
- 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
- B60C1/0016—Compositions of the tread
Definitions
- the present disclosure relates to methods for adhering rubber compositions to polyurethane to form a rubber-polyurethane composite and, more particularly, rubber compositions containing a carbamate resin adhered to a polyurethane substrate.
- a composite that includes at least two layers.
- One layer is a rubber layer having a first layer surface and the rubber layer also includes an adhesion-promoting composition and the adhesion-promoting composition contains an alkyl urethane and an aldehyde.
- the second layer is a polyurethane substrate that is adjacent to the rubber layer and also has a first substrate surface.
- the alkyl urethane is butyl urethane.
- the aldehyde is formaldehyde.
- the molar ratio of aldehyde to alkyl urethane is from
- the rubber layer contains 0.1 to 10 weight parts of the adhesion-promoting composition per 100 weight parts of rubber.
- the rubber layer contains at least 2 weight parts of the adhesion-promoting composition per 100 weight parts of rubber.
- the first layer surface of the rubber layer is facing the first substrate surface of the polyurethane substrate.
- the first substrate surface of the polyurethane substrate layer is in direct contact with the first layer surface of the rubber layer.
- the rubber layer includes a tread surface.
- the rubber layer underlies a tread portion of a tire.
- the composite is a portion of a tire.
- the tire is a non-pneumatic tire.
- the polyurethane substrate includes at least 90 weight percent of polyurethane.
- the rubber layer also includes a reinforcing filler such as carbon black or silica.
- the rubber layer also includes styrene butadiene rubber, polyisoprene rubber, polybutadiene rubber, or natural rubber.
- the first aspect may be provided alone or in combination with any one or more of the examples of the first aspect discussed above.
- the rubber composition is adhered to a polyurethane substrate by a) mixing a composition, which includes an alkyl urethane and an aldehyde, with a rubber compound to form a treated rubber compound; b) curing the treated rubber compound by heating to form a cured rubber compound; c) contacting the cured rubber compound to the polyurethane substrate to form a composite; and d) heating the composite of the cured rubber compound and the polyurethane substrate.
- a composition which includes an alkyl urethane and an aldehyde
- the aldehyde is formaldehyde.
- the molar ratio of the aldehyde to the alkyl urethane is from 0.1: 1 to 0.5: 1.
- the treated rubber compound including 0.1 to 10 weight parts of the composition per 100 weight parts of rubber.
- the composition is present in the treated rubber compound in at least 2 weight parts per 100 weight parts of rubber.
- step 'b' includes maintaining the treated rubber compound at a temperature in the range of 130° C to 180° C for a time period in the range of 15 minutes to 45 minutes.
- step 'd' includes maintaining the composite at a temperature in the range of 130° C to 180° C for a time period in the range of 15 minutes to 45 minutes.
- the composite is a portion of a tire.
- the second aspect may be provided alone or in combination with any one or more of the examples of the second aspect discussed above, or with any one or more of the examples of the first aspect.
- the accompanying drawing is included to provide a further understanding of principles of the invention, and is incorporated in and constitutes a part of this specification.
- the drawing illustrates one or more embodiment(s), and together with the description serves to explain, by way of example, principles and operation of the invention. It is to be understood that various features disclosed in this specification and in the drawing can be used in any and all combinations. By way of non-limiting example the various features may be combined with one another as set forth in the specification as aspects.
- FIG. 1 shows the adhesion strength (N/in) of a rubber layer adhered to a polyurethane substrate.
- a range such as 5-25 (or 5 to 25) is given, this means preferably at least or more than 5 and, separately and independently, preferably not more than or less than 25. In an example, such a range defines independently at least 5, and separately and independently, not more than 25.
- the term “phr” means the parts by weight of rubber. If the rubber composition comprises more than one rubber, “phr” means the parts by weight per hundred parts of the sum of all rubbers.
- the present disclosure relates to the adhesion of elastomer or rubber compositions, such as a rubber-containing layer or vulcanizable rubber compositions, to polyurethane compositions.
- elastomer and rubber will be used interchangeably in this specification.
- the adhesion between the rubber composition and the polyurethane composition can be accomplished without the presence of a separate adhesive composition application, for example, disposed between the two compositions being adhered.
- the rubber-containing compositions preferably include an adhesion-promoting composition, for example a composition containing a carbamate compound.
- the present disclosure provides a rubber-polyurethane composite having the two layers adhered to one another, preferably without the presence of a separate adhesive formation or application steps.
- the present disclosure shows that modifying a rubber mixture by incorporating an adhesion- promoting composition provides a rubber surface that is ready to be bonded to a polyurethane substrate.
- the modified rubber mixture can be further treated by curing the modified rubber compound and optionally buffing (e.g., with a sander) the adhesion surface.
- the adhesion- promoting composition may not function as an adhesive by itself, as in the case of polyurethane adhesives, but it can enhance the adhesion of a rubber composition to a polyurethane substrate and thus function as an adhesive in a rubber-containing composition.
- the elastomeric composition can include one or more elastomeric materials.
- elastomeric materials a variety of materials may be utilized as the elastomeric or rubber layer. Examples include polybutadiene, polyisoprene, natural rubber, ethylene-propylene diene copolymers (EPDM), ethylene-propylene copolymers, ethylene-propylene-diene terpolymers, polysulfide polymers, polyurethane elastomers, chloro sulfonated polyethylene, polychloroprene, plasticized polyvinylchloride, butadiene acrylonitrile elastomers, poly(isobutylene-co-isoprene), polyacrylates, polyesters, polyethers, fluoroelastomers, silicone elastomers, copolymers of ethylene, and combinations thereof, and other low modulus polymers and copolymers. Also useful are blends of different elastomeric materials, or blends of
- block copolymers of conjugated dienes and vinyl aromatic monomers can be used to form the rubber layer.
- Butadiene and isoprene are preferred conjugated diene elastomers.
- Styrene, vinyl toluene and t-butyl styrene are preferred conjugated aromatic monomers.
- Block copolymers incorporating polyisoprene may be hydrogenated to produce thermoplastic elastomers.
- the rubber layer can be a rubber layer including a rubber compound selected from the group consisting of a blend of natural rubber and styrene butadiene; a blend of natural rubber and polybutadiene; and a blend of natural rubber, styrene butadiene, and polybutadiene.
- At least 60% by weight (at least 60 phr), at least 70% by weight (at least 70 phr), at least 80% by weight (at least 80 phr), at least 90% by weight (at least 90 phr), at least 95% by weight (at least 95 phr), or even 100% by weight (100 phr) of the rubber composition contains at least one of: natural rubber, synthetic polyisoprene rubber,
- the rubber compositions of the present disclosure may further include, if desired, various appropriate additional compounding ingredients as known in the art, e.g., oils, pigments, extenders, surfactants, stabilizers, softeners (e.g., wax, stearic acid, zinc), resins (adhesives), vulcanizing agents (e.g., sulfur) and anti-oxidants.
- additional compounding ingredients e.g., oils, pigments, extenders, surfactants, stabilizers, softeners (e.g., wax, stearic acid, zinc), resins (adhesives), vulcanizing agents (e.g., sulfur) and anti-oxidants.
- non-carbon black reinforcing agent such as silica, clay or calcium carbonate may be used in an appropriate amount in combination with carbon black.
- the rubber composition can include 5 to 200 phr of at least one reinforcing filler.
- One or more than one reinforcing filler may be utilized in the rubber compositions according to the embodiments disclosed herein.
- the total amount of the reinforcing filler is 5 to 200 phr, including 10 to 200 phr, 10 to 175 phr, 25 to 150 phr, 35 to 150 phr, 25 to 125 phr, 25 to 100 phr of at least one reinforcing filler.
- the at least one reinforcing filler includes at least one of: carbon black or silica.
- the at least one reinforcing filler includes at least one carbon black, at least one silica, or at least one carbon black and at least one silica.
- the at least one reinforcing filler includes at least one of: carbon black or silica, and further includes at least one additional reinforcing filler.
- the at least one reinforcing filler includes at least one carbon black and at least one additional reinforcing filler (other than silica), at least one silica and at least one additional reinforcing filler (other than carbon black), or at least one silica and at least one carbon black and at least one additional reinforcing filler (other than the carbon black or silica).
- the rubber composition may include an adhesion- promoting composition for promoting adhesion of the rubber composition to polyurethane.
- the adhesion-promoting composition can be a carbamate or urethane compound.
- the adhesion-promoting composition includes alkyl urethane, an aldehyde or mixtures of an alkyl urethane and an aldehyde.
- the adhesion-promoting composition can include an alkyl urethane and an aldehyde and no other components.
- the molar ratio of alkyl urethane to aldehyde in the adhesion-promoting composition can be from 1:0.1 to 1:0.5, and preferably from 1:0.2 to 1:0.4.
- the adhesion-promoting composition may be added to the rubber composition to provide an enhanced adhesion property to the rubber composition, and in particular, an increased adhesion to polyurethane as compared to the same rubber composition without the incorporation of the adhesion-promoting composition.
- the rubber compositions of the present disclosure can contain an adhesion-promoting composition in an amount of 0.1 to 15 phr, 0.5 to 12 phr, 1 to 10 phr, 2 to 8 phr or 3, 4, 5, 6 or 7 phr.
- the alkyl urethane in the adhesion-promoting composition can be selected from the below chemical structure.
- alkyl urethane suitable for inclusion in the adhesion-promoting composition examples include propyl carbamate, butyl carbamate, pentyl carbamate and combinations thereof.
- the aldehyde in the adhesion-promoting composition can be, for example, formaldehyde or acetaldehyde.
- the adhesion-promoting composition can include a combination of butyl carbamate or urethane and formaldehyde, for example, at a butyl carbamate to formaldehyde ratio of 1:0.1 to 1:0.5.
- the rubber compositions of the present disclosure can be in the form of any suitable shape, for example, a layer, that can be brought into contact with a polyurethane compound for adhering the rubber composition to the polyurethane compound.
- the rubber composition can be in the form of a tire component.
- tire components can include treads, sidewalls, or a carcass.
- the rubber composition containing the adhesion-promoting component is bonded to a polyurethane.
- the rubber composition can be in the form of a rubber layer having a surface for contacting the polyurethane, which can be in the form of a compound or layer (e.g., substrate) having a surface for contacting the rubber composition.
- a variety of polyurethane compositions, including mixtures thereof, may be employed in the present disclosure for adhering to the rubber compositions.
- polyurethane compositions can be formed by the combination of various diisocyanates, and/or polymeric isocyanates with various monomeric alcohols and/or polymeric alcohols.
- diisocyanates include but are not limited to toluene diisocyanates, xylene diisocyanates, cumene diisocyanates, methylene diphenyl diisocyanates, hexamethylene diisocyanates, tetramethylene diisocyanates, phenylene diisocyanates, chlorophenyl
- Examples of monomeric alcohols include but are not limited to ethylene glycol, 1,3- propanediol, 1,4-butanediol, 1,5-pentanediol, and 1,6-hexanediol.
- polymeric alcohols include but are not limited to polymeric ether and/or ester diols such as a polypropylene glycol, a polyadipate diol, a polycaprolactone diol, a polyphthalate diol, and a polycarbonate diol.
- polymeric ether and/or ester diols such as a polypropylene glycol, a polyadipate diol, a polycaprolactone diol, a polyphthalate diol, and a polycarbonate diol.
- the polyurethane compositions contain at least 80, 90 or 95 weight percent of polyurethane.
- the polyurethane in contact with the rubber composition can be entirely composed of polyurethane and no other non-urethane ingredients.
- the polyurethane compositions can also include fillers to obtain the desired physical properties of the polyurethane composition. Such fillers include but are not limited to carbon black, titanium dioxide, zinc oxide, calcium carbonate, silicas, and coloring pigments.
- the polyurethane compositions of the present disclosure can be in the form of any suitable shape, for example, a layer or substrate, that can be brought into contact with a rubber composition for adhering the polyurethane to the rubber compound.
- the polyurethane composition can be in the form of a tire component, for example a rim or wheel support.
- the polyurethane can be adhered to the rubber compositions by a variety of methods.
- the rubber-polyurethane composite can be prepared by a stepwise process.
- the process can include one or more of the following steps.
- the adhesion-promoting composition e.g., a mixture of an alkyl urethane and an aldehyde, can be incorporated into an uncured rubber-containing composition to form a treated rubber composition.
- the treated rubber composition can be subjected to a heat cycle, for example under pressure, to give a cured rubber composition suitable for adhering to a polyurethane.
- a heat cycle can include heating a composition, for example from ambient temperature, to a temperature of between 130 ° C and 180° C, optionally under a pressure from 50-150 psi, and maintaining the composition at the heated temperature for a period between 15 minutes to 2 hours or 15 minutes and 1 hours, preferably between 145° C and 165° C, optionally at a pressure from 75-125 psi, for a period between 20 minutes and 45 minutes.
- the cured rubber composition can be cooled, for example, to ambient temperature, prior to the next optional process step.
- the bonding surfaces of the cured rubber composition and polyurethane composition i.e. the surfaces that contact one another
- the bonding surfaces of the cured rubber composition and polyurethane composition can be buffed to provide a clean surface and roughened for adhesion.
- the bonding surfaces can be buffed with a sander such as a hand-held sander.
- the contact or bonding surfaces of the cured rubber and polyurethane are brought together and the two surfaces in contact with one another are subjected to a heat cycle as described above, for instance, under pressure, to form the composite.
- the composite can then be cooled to room temperature.
- the treated rubber composition in an uncured state can be brought into contact with the polyurethane at a suitable temperature and subjected to a heat cycle, preferably under pressure, to form the composite of the rubber composition adhered to the polyurethane.
- the final heat cycle can complete the adhesion process and give a final composite that, once cooled, may have useful properties for a variety of applications that require the flexibility or grip of rubber and the durability of polyurethane, for example, hoses, drive belts, and pneumatic or non-pneumatic tires.
- the adhesion of the rubber layer and polyurethane substrate can be achieved using the present disclosure where the rubber layer can serve as the tread of the tire or another tire component, e.g., the portion that underlies the tread, and the polyurethane layer can serve as the tire casing or support structure.
- the formed composite structure itself can be in the form of a tire or tire component.
- the heat-treated composite exhibits improved adhesion between the two bonded layers of the rubber composition and the polyurethane, for example, as observed in a T-peel adhesion test, ASTM D1876. Additionally, the composite can show minimal blooming which otherwise could negatively affect the adhesive tack between the two compositions.
- the composite of the present disclosure exhibits an adhesion strength between the contact surfaces of the rubber composition containing an adhesion-promoting composition and the polyurethane of at least 5, 10, 15, 20, 25, 30, 35, 40, 45 or 50 percent higher than the adhesion of the same rubber composition absent the adhesion- promoting composition to the same polyurethane.
- the composite of the present disclosure exhibits an adhesion strength between the contact surfaces of the rubber composition containing an adhesion-promoting composition and the polyurethane of at least 5, 10, 15, 20, 25, 30, 35, 40, 45 or 50 Newton/in higher than the adhesion of the same rubber composition absent the adhesion-promoting composition to the same polyurethane.
- FIG. 1, as described below in the Example indicates the adhesion strength in Newton per inch measured for multiple rubber compositions adhered to a polyurethane substrate.
- the uncured rubber compound was then divided into 4 batches. A 1:0.3 mole ratio of a butylurethane: formaldehyde mixture was then added separately to 3 of the 4 batches of uncured rubber compound in amounts of 2, 5, and 10 phr respectively with the last batch of uncured rubber compound containing no butylurethane: formaldehyde mixture. Each batch was separately cured at 145° C for 33 minutes at 100 psi. The resulting cured rubber compound was then prepared for adhesion by buffing of the bonding surface. Buffing of the surfaces was carried out with a hand-held orbital sander for a sufficient period of time until the surface was visibly changed by the sanding.
- the bonding surface of the polyurethane substrate was also buffed.
- the buffed bonding surface of the cured rubber compound was then laminated to the buffed bonding surface of the polyurethane substrate and the resulting laminate was cured at 145° C for 33 minutes at 100 psi.
- the polyurethane substrate was based on a mixture of 19.2% toluene diisocyanate and 80.8% tetramethylene glycol.
- the adhesion strength of the resulting cured rubber-polyurethane composite was measured by a T-peel test using the ASTM D1876 procedure. The rubber-polyurethanesion strength based on loading of the
- butylurethane formaldehyde mixture is shown in FIG. 1.
- the composite made with 0 phr of butylurethane: formaldehyde mixture is the baseline measurement of 0 Newton per inch for the T-peel test used in the
- the cured rubber composition containing 2 phr of the butylurethane: formaldehyde mixture exhibited an increased adhesion strength to the polyurethane of about 15% greater than the baseline composite, or about 15 Newton per inch greater peel strength.
- the rubber composition containing 5 phr of the butylurethane: formaldehyde mixture exhibited an increased adhesion strength to the polyurethane of about 40% greater than the baseline composite, or about 40 Newton per inch greater peel strength.
- the rubber composition containing 10 phr of the butylurethane:formaldehyde mixture exhibited an increased adhesion strength to the polyurethane of about 5% greater than the baseline composite, or about 5 Newton per inch greater peel strength.
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Abstract
A composite of a rubber layer and a polyurethane substrate are adhered together without the need for a separate adhesive layer. An adhesion-promoting composition incorporated into the rubber layer provides the means for adhereing the rubber layer to the polyurethane substrate. The adhered layered composition may be used in many applications including the construction of tires.
Description
CARBAMATE RESIN FOR POLYURETHANE ADHESION
TECHNICAL FIELD
[001] The present disclosure relates to methods for adhering rubber compositions to polyurethane to form a rubber-polyurethane composite and, more particularly, rubber compositions containing a carbamate resin adhered to a polyurethane substrate.
BACKGROUND
[002] Achieving high bond strength in the adhering of dissimilar materials such as cured rubber and polyurethane has been known to be difficult. For instance, an intermolecular interaction of the polar nature of a polyurethane surface and the non-polar nature of a cured olefinic rubber surface is not favorable at the interface of the two different surfaces. Various methods have been developed thus far to improve the adhesion of polyurethane to cured olefinic rubber. However, these methods usually rely on the separate application of an adhesive composition, which may include multiple components, to at least one of the surfaces being adhered together and thus forming an adhesive layer. These adhesives are typically based on polyurethanes or polyisocyanates that undergo a chemical reaction to form a polyurethane.
[003] It is an objective of the present disclosure to alleviate or overcome one or more difficulties related to the prior art. It has been found that an adhesion between a rubber composition and a polyurethane substrate can be achieved without the need for a surface application of a separate adhesive composition. The incorporation of an adhesion-promoting composition that includes an alkyl urethane and an aldehyde into a rubber compound provides enhanced adhesion between a rubber composition and a polyurethane substrate.
SUMMARY
[004] In a first aspect, there is a composite that includes at least two layers. One layer is a rubber layer having a first layer surface and the rubber layer also includes an adhesion-promoting composition and the adhesion-promoting composition contains an alkyl urethane and an aldehyde. The second layer is a polyurethane substrate that is adjacent to the rubber layer and also has a first substrate surface.
[006] In another example of aspect 1, the alkyl urethane is butyl urethane.
[007] In another example of aspect 1, the aldehyde is formaldehyde.
[008] In another example of aspect 1, the molar ratio of aldehyde to alkyl urethane is from
0.1: 1 to 0.5: 1.
[009] In another example of aspect 1, the rubber layer contains 0.1 to 10 weight parts of the adhesion-promoting composition per 100 weight parts of rubber.
[0010] In another example of aspect 1, the rubber layer contains at least 2 weight parts of the adhesion-promoting composition per 100 weight parts of rubber.
[0011] In another example of aspect 1, the first layer surface of the rubber layer is facing the first substrate surface of the polyurethane substrate.
[0012] In another example of aspect 1, the first substrate surface of the polyurethane substrate layer is in direct contact with the first layer surface of the rubber layer.
[0013] In another example of aspect 1, the rubber layer includes a tread surface.
[0014] In another example of aspect 1, the rubber layer underlies a tread portion of a tire.
[0015] In another example of aspect 1, the composite is a portion of a tire.
[0016] In another example of aspect 1, the tire is a non-pneumatic tire.
[0017] In another example of aspect 1, the polyurethane substrate includes at least 90 weight percent of polyurethane.
[0018] In another example of aspect 1, the rubber layer also includes a reinforcing filler such as carbon black or silica.
[0019] In another example of aspect 1, the rubber layer also includes styrene butadiene rubber, polyisoprene rubber, polybutadiene rubber, or natural rubber.
[0020] The first aspect may be provided alone or in combination with any one or more of the examples of the first aspect discussed above.
[0021] In a second aspect, the rubber composition is adhered to a polyurethane substrate by a) mixing a composition, which includes an alkyl urethane and an aldehyde, with a rubber compound to form a treated rubber compound; b) curing the treated rubber compound by heating to form a cured rubber compound; c) contacting the cured rubber compound to the polyurethane substrate to form a composite; and d) heating the composite of the cured rubber compound and the polyurethane substrate.
[0023] In another example of aspect 2, the aldehyde is formaldehyde.
[0024] In another example of aspect 2, the molar ratio of the aldehyde to the alkyl urethane is from 0.1: 1 to 0.5: 1.
[0025] In another example of aspect 2, the treated rubber compound including 0.1 to 10 weight parts of the composition per 100 weight parts of rubber.
[0026] In another example of aspect 2, the composition is present in the treated rubber compound in at least 2 weight parts per 100 weight parts of rubber.
[0027] In another example of aspect 2, step 'b' includes maintaining the treated rubber compound at a temperature in the range of 130° C to 180° C for a time period in the range of 15 minutes to 45 minutes.
[0028] In another example of aspect 2, step 'd' includes maintaining the composite at a temperature in the range of 130° C to 180° C for a time period in the range of 15 minutes to 45 minutes.
[0029] In another example of aspect 2, the composite is a portion of a tire.
[0030] The second aspect may be provided alone or in combination with any one or more of the examples of the second aspect discussed above, or with any one or more of the examples of the first aspect. The accompanying drawing is included to provide a further understanding of principles of the invention, and is incorporated in and constitutes a part of this specification. The drawing illustrates one or more embodiment(s), and together with the description serves to explain, by way of example, principles and operation of the invention. It is to be understood that various features disclosed in this specification and in the drawing can be used in any and all combinations. By way of non-limiting example the various features may be combined with one another as set forth in the specification as aspects.
BRIEF DESCRIPTION OF THE DRAWING
[0031] The above description and other features, aspects and advantages are better understood when the following detailed description is read with reference to the accompanying drawings, in which:
[0032] FIG. 1 shows the adhesion strength (N/in) of a rubber layer adhered to a polyurethane substrate.
DETAILED DESCRIPTION
[0033] The terminology as set forth herein is for description of the embodiments only and should not be construed as limiting the invention as a whole.
[0034] Herein, when a range such as 5-25 (or 5 to 25) is given, this means preferably at least or more than 5 and, separately and independently, preferably not more than or less than 25. In an example, such a range defines independently at least 5, and separately and independently, not more than 25.
[0035] As used herein, the term "phr" means the parts by weight of rubber. If the rubber composition comprises more than one rubber, "phr" means the parts by weight per hundred parts of the sum of all rubbers.
[0036] The present disclosure relates to the adhesion of elastomer or rubber compositions, such as a rubber-containing layer or vulcanizable rubber compositions, to polyurethane compositions. The terms elastomer and rubber will be used interchangeably in this specification. The adhesion between the rubber composition and the polyurethane composition can be accomplished without the presence of a separate adhesive composition application, for example, disposed between the two compositions being adhered. The rubber-containing compositions preferably include an adhesion-promoting composition, for example a composition containing a carbamate compound.
[0037] In general, common adhesives are used for adhering rubber to polyurethane. Such adhesives have been based on polyurethanes by means of a chemical reaction between a diisocyanate and an alcohol, such as a diol, with the optional use of a curative agent such as a diamine. The bonding surfaces of the rubber and polyurethane compositions are then prepared by a buffing process that cleans and abrades the bonding surface. The bonding surfaces sometimes need an initial application of a priming agent before the adhesive is applied. The polyurethane adhesive then has to be applied at a desired thickness to at least one and perhaps both of the buffed bonding surfaces of the rubber and/or polyurethane substrate. The present disclosure provides a rubber-polyurethane composite having the two layers adhered to one another, preferably without the presence of a separate adhesive formation or application steps. The present disclosure shows that modifying a rubber mixture by incorporating an adhesion- promoting composition provides a rubber surface that is ready to be bonded to a polyurethane substrate. The modified rubber mixture can be further treated by curing the modified rubber compound and optionally buffing (e.g., with a sander) the adhesion surface. The adhesion- promoting composition may not function as an adhesive by itself, as in the case of polyurethane adhesives, but it can enhance the adhesion of a rubber composition to a polyurethane substrate and thus function as an adhesive in a rubber-containing composition.
[0038] The elastomeric composition can include one or more elastomeric materials. For example, a variety of materials may be utilized as the elastomeric or rubber layer. Examples include polybutadiene, polyisoprene, natural rubber, ethylene-propylene diene copolymers (EPDM), ethylene-propylene copolymers, ethylene-propylene-diene terpolymers, polysulfide polymers, polyurethane elastomers, chloro sulfonated polyethylene, polychloroprene, plasticized polyvinylchloride, butadiene acrylonitrile elastomers, poly(isobutylene-co-isoprene),
polyacrylates, polyesters, polyethers, fluoroelastomers, silicone elastomers, copolymers of ethylene, and combinations thereof, and other low modulus polymers and copolymers. Also useful are blends of different elastomeric materials, or blends of elastomeric materials.
[0039] In one or more embodiments, block copolymers of conjugated dienes and vinyl aromatic monomers can be used to form the rubber layer. Butadiene and isoprene are preferred conjugated diene elastomers. Styrene, vinyl toluene and t-butyl styrene are preferred conjugated aromatic monomers. Block copolymers incorporating polyisoprene may be hydrogenated to produce thermoplastic elastomers.
[0040] In another embodiment, the rubber layer can be a rubber layer including a rubber compound selected from the group consisting of a blend of natural rubber and styrene butadiene; a blend of natural rubber and polybutadiene; and a blend of natural rubber, styrene butadiene, and polybutadiene.
[0041] In certain embodiments, at least 60% by weight (at least 60 phr), at least 70% by weight (at least 70 phr), at least 80% by weight (at least 80 phr), at least 90% by weight (at least 90 phr), at least 95% by weight (at least 95 phr), or even 100% by weight (100 phr) of the rubber composition contains at least one of: natural rubber, synthetic polyisoprene rubber,
polybutadiene rubber, and styrene-butadiene rubber.
[0042] The rubber compositions of the present disclosure may further include, if desired, various appropriate additional compounding ingredients as known in the art, e.g., oils, pigments, extenders, surfactants, stabilizers, softeners (e.g., wax, stearic acid, zinc), resins (adhesives), vulcanizing agents (e.g., sulfur) and anti-oxidants. In another example, non-carbon black reinforcing agent such as silica, clay or calcium carbonate may be used in an appropriate amount in combination with carbon black.
[0043] In one or more embodiments, the rubber composition can include 5 to 200 phr of at least one reinforcing filler. One or more than one reinforcing filler may be utilized in the rubber compositions according to the embodiments disclosed herein. In certain embodiments disclosed herein, the total amount of the reinforcing filler is 5 to 200 phr, including 10 to 200 phr, 10 to 175 phr, 25 to 150 phr, 35 to 150 phr, 25 to 125 phr, 25 to 100 phr of at least one reinforcing filler. In certain embodiments disclosed herein, the at least one reinforcing filler includes at least one of: carbon black or silica. In such embodiments, the at least one reinforcing filler includes at least one carbon black, at least one silica, or at least one carbon black and at least one silica. In
certain embodiments disclosed herein, the at least one reinforcing filler includes at least one of: carbon black or silica, and further includes at least one additional reinforcing filler. In such embodiments, the at least one reinforcing filler includes at least one carbon black and at least one additional reinforcing filler (other than silica), at least one silica and at least one additional reinforcing filler (other than carbon black), or at least one silica and at least one carbon black and at least one additional reinforcing filler (other than the carbon black or silica).
[0044] In one or more embodiments, the rubber composition may include an adhesion- promoting composition for promoting adhesion of the rubber composition to polyurethane. In one example, the adhesion-promoting composition can be a carbamate or urethane compound. Preferably, the adhesion-promoting composition includes alkyl urethane, an aldehyde or mixtures of an alkyl urethane and an aldehyde. In one example, the adhesion-promoting composition can include an alkyl urethane and an aldehyde and no other components. The molar ratio of alkyl urethane to aldehyde in the adhesion-promoting composition can be from 1:0.1 to 1:0.5, and preferably from 1:0.2 to 1:0.4.
[0045] The adhesion-promoting composition may be added to the rubber composition to provide an enhanced adhesion property to the rubber composition, and in particular, an increased adhesion to polyurethane as compared to the same rubber composition without the incorporation of the adhesion-promoting composition. In one or more embodiments, the rubber compositions of the present disclosure can contain an adhesion-promoting composition in an amount of 0.1 to 15 phr, 0.5 to 12 phr, 1 to 10 phr, 2 to 8 phr or 3, 4, 5, 6 or 7 phr.
[0046] The alkyl urethane in the adhesion-promoting composition can be selected from the below chemical structure.
[0047] Examples of an alkyl urethane suitable for inclusion in the adhesion-promoting composition include propyl carbamate, butyl carbamate, pentyl carbamate and combinations thereof.
[0048] The aldehyde in the adhesion-promoting composition can be, for example, formaldehyde or acetaldehyde.
[0049] In one embodiment, the adhesion-promoting composition can include a combination of butyl carbamate or urethane and formaldehyde, for example, at a butyl carbamate to formaldehyde ratio of 1:0.1 to 1:0.5.
[0050] The rubber compositions of the present disclosure can be in the form of any suitable shape, for example, a layer, that can be brought into contact with a polyurethane compound for adhering the rubber composition to the polyurethane compound. In one example, the rubber composition can be in the form of a tire component. Some examples of tire components can include treads, sidewalls, or a carcass.
[0051] To form the composite, the rubber composition containing the adhesion-promoting component is bonded to a polyurethane. For example, the rubber composition can be in the form of a rubber layer having a surface for contacting the polyurethane, which can be in the form of a compound or layer (e.g., substrate) having a surface for contacting the rubber composition. A variety of polyurethane compositions, including mixtures thereof, may be employed in the present disclosure for adhering to the rubber compositions. For instance, polyurethane compositions can be formed by the combination of various diisocyanates, and/or polymeric isocyanates with various monomeric alcohols and/or polymeric alcohols.
[0052] Examples of diisocyanates include but are not limited to toluene diisocyanates, xylene diisocyanates, cumene diisocyanates, methylene diphenyl diisocyanates, hexamethylene diisocyanates, tetramethylene diisocyanates, phenylene diisocyanates, chlorophenyl
diisocyanates, cyclohexylene diisocyanates, and methylene bis-cyclohexylene diisocyanates.
[0053] Examples of monomeric alcohols include but are not limited to ethylene glycol, 1,3- propanediol, 1,4-butanediol, 1,5-pentanediol, and 1,6-hexanediol.
[0054] Examples of polymeric alcohols include but are not limited to polymeric ether and/or ester diols such as a polypropylene glycol, a polyadipate diol, a polycaprolactone diol, a polyphthalate diol, and a polycarbonate diol.
[0055] The polyurethane compositions contain at least 80, 90 or 95 weight percent of polyurethane. In one example, the polyurethane in contact with the rubber composition can be entirely composed of polyurethane and no other non-urethane ingredients. The polyurethane compositions can also include fillers to obtain the desired physical properties of the polyurethane
composition. Such fillers include but are not limited to carbon black, titanium dioxide, zinc oxide, calcium carbonate, silicas, and coloring pigments.
[0056] The polyurethane compositions of the present disclosure can be in the form of any suitable shape, for example, a layer or substrate, that can be brought into contact with a rubber composition for adhering the polyurethane to the rubber compound. In one example, the polyurethane composition can be in the form of a tire component, for example a rim or wheel support.
[0057] The polyurethane can be adhered to the rubber compositions by a variety of methods. In one embodiment, the rubber-polyurethane composite can be prepared by a stepwise process. The process can include one or more of the following steps. The adhesion-promoting composition, e.g., a mixture of an alkyl urethane and an aldehyde, can be incorporated into an uncured rubber-containing composition to form a treated rubber composition. The treated rubber composition can be subjected to a heat cycle, for example under pressure, to give a cured rubber composition suitable for adhering to a polyurethane. A heat cycle, as used herein, can include heating a composition, for example from ambient temperature, to a temperature of between 130° C and 180° C, optionally under a pressure from 50-150 psi, and maintaining the composition at the heated temperature for a period between 15 minutes to 2 hours or 15 minutes and 1 hours, preferably between 145° C and 165° C, optionally at a pressure from 75-125 psi, for a period between 20 minutes and 45 minutes.
[0058] The cured rubber composition can be cooled, for example, to ambient temperature, prior to the next optional process step. The bonding surfaces of the cured rubber composition and polyurethane composition (i.e. the surfaces that contact one another) can be buffed to provide a clean surface and roughened for adhesion. For example, the bonding surfaces can be buffed with a sander such as a hand-held sander. The contact or bonding surfaces of the cured rubber and polyurethane are brought together and the two surfaces in contact with one another are subjected to a heat cycle as described above, for instance, under pressure, to form the composite. The composite can then be cooled to room temperature. In another example, the treated rubber composition in an uncured state can be brought into contact with the polyurethane at a suitable temperature and subjected to a heat cycle, preferably under pressure, to form the composite of the rubber composition adhered to the polyurethane.
[0059] The final heat cycle can complete the adhesion process and give a final composite that, once cooled, may have useful properties for a variety of applications that require the flexibility or grip of rubber and the durability of polyurethane, for example, hoses, drive belts, and pneumatic or non-pneumatic tires. In the case of tire construction, the adhesion of the rubber layer and polyurethane substrate can be achieved using the present disclosure where the rubber layer can serve as the tread of the tire or another tire component, e.g., the portion that underlies the tread, and the polyurethane layer can serve as the tire casing or support structure. Thus, the formed composite structure itself can be in the form of a tire or tire component.
[0060] The heat-treated composite exhibits improved adhesion between the two bonded layers of the rubber composition and the polyurethane, for example, as observed in a T-peel adhesion test, ASTM D1876. Additionally, the composite can show minimal blooming which otherwise could negatively affect the adhesive tack between the two compositions.
[0061] In one or more embodiments, the composite of the present disclosure exhibits an adhesion strength between the contact surfaces of the rubber composition containing an adhesion-promoting composition and the polyurethane of at least 5, 10, 15, 20, 25, 30, 35, 40, 45 or 50 percent higher than the adhesion of the same rubber composition absent the adhesion- promoting composition to the same polyurethane. In another embodiment, the composite of the present disclosure exhibits an adhesion strength between the contact surfaces of the rubber composition containing an adhesion-promoting composition and the polyurethane of at least 5, 10, 15, 20, 25, 30, 35, 40, 45 or 50 Newton/in higher than the adhesion of the same rubber composition absent the adhesion-promoting composition to the same polyurethane. FIG. 1, as described below in the Example, indicates the adhesion strength in Newton per inch measured for multiple rubber compositions adhered to a polyurethane substrate.
[0062] EXAMPLES
[0063] The following examples illustrate specific and exemplary embodiments and/or features of the embodiments of the present disclosure. The examples are provided solely for the purposes of illustration and should not be construed as limitations of the present disclosure. Numerous variations over these specific examples are possible without departing from the spirit and scope of the presently disclosed embodiments. More specifically, the particular rubbers,
fillers, and other ingredients (e.g., antioxidant, curative, etc.) utilized in the examples should not be interpreted as limiting since other such ingredients consistent with the disclosure in the Detailed Description can utilized in substitution. That is, the particular ingredients in the compositions, as well as their respective amounts and relative amounts should be understood to apply to the more general content of the Detailed Description.
[0064] EXAMPLE 1
[0065] Preparation of modified cured rubber layer
[0066] The following components were combined in the proportions given in Table 1 and mixed at room temperature for a sufficient period of time to give an uncured rubber compound.
[0067] Table 1: Uncured rubber composition
„ Amount
Comp0nent used (PHR)
Natural Rubber 10
Synthetic Rubber 90
Filler 75
Softeners 30
Curatives 10
[0068] The uncured rubber compound was then divided into 4 batches. A 1:0.3 mole ratio of a butylurethane: formaldehyde mixture was then added separately to 3 of the 4 batches of uncured rubber compound in amounts of 2, 5, and 10 phr respectively with the last batch of uncured rubber compound containing no butylurethane: formaldehyde mixture. Each batch was separately cured at 145° C for 33 minutes at 100 psi. The resulting cured rubber compound was then prepared for adhesion by buffing of the bonding surface. Buffing of the surfaces was carried out with a hand-held orbital sander for a sufficient period of time until the surface was visibly changed by the sanding. The bonding surface of the polyurethane substrate was also buffed. The buffed bonding surface of the cured rubber compound was then laminated to the buffed bonding surface of the polyurethane substrate and the resulting laminate was cured at 145° C for 33 minutes at 100 psi. The polyurethane substrate was based on a mixture of 19.2%
toluene diisocyanate and 80.8% tetramethylene glycol. The adhesion strength of the resulting cured rubber-polyurethane composite was measured by a T-peel test using the ASTM D1876 procedure. The rubber-polyurethane adhesion strength based on loading of the
butylurethane: formaldehyde mixture is shown in FIG. 1.
[0069] As shown in FIG. 1, the composite made with 0 phr of butylurethane: formaldehyde mixture is the baseline measurement of 0 Newton per inch for the T-peel test used in the
Examples. The cured rubber composition containing 2 phr of the butylurethane: formaldehyde mixture exhibited an increased adhesion strength to the polyurethane of about 15% greater than the baseline composite, or about 15 Newton per inch greater peel strength. The rubber composition containing 5 phr of the butylurethane: formaldehyde mixture exhibited an increased adhesion strength to the polyurethane of about 40% greater than the baseline composite, or about 40 Newton per inch greater peel strength. Lastly, the rubber composition containing 10 phr of the butylurethane:formaldehyde mixture exhibited an increased adhesion strength to the polyurethane of about 5% greater than the baseline composite, or about 5 Newton per inch greater peel strength.
[0070] All references, including but not limited to patents, patent applications, and nonpatent literature are hereby incorporated by reference herein in their entirety.
[0071] While various aspects and embodiments of the compositions and methods have been disclosed herein, other aspects and embodiments will be apparent to those skilled in the art. The various aspects and embodiments disclosed herein are for purposes of illustration and are not intended to be limiting, with the true scope and spirit being indicated by the claims.
Claims
1. A composite comprising:
a. a rubber layer, the rubber layer having a first layer surface and the rubber layer comprising an adhesion-promoting composition, the adhesion-promoting composition comprising an alkyl urethane and an aldehyde; and
b. a polyurethane substrate adjacent to the rubber layer, the polyurethane substrate having a first substrate surface.
3. The composite of claim 1, the alkyl urethane being butyl urethane.
4. The composite of claim 1, the aldehyde being formaldehyde.
5. The composite of claim 1, the molar ratio of the aldehyde to the alkyl urethane being from 0.1: 1 to 0.5: 1 and the rubber layer comprising 2 to 10 weight parts of the adhesion- promoting composition per 100 weight parts of rubber.
6. The composite of claim 5, the adhesion-promoting composition being present in the rubber layer in at least 2 weight parts per 100 weight parts of rubber.
7. The composite of claim 1, the first layer surface of the rubber layer facing the first
substrate surface of the polyurethane substrate.
8. The composite of claim 7, the first substrate surface of the polyurethane substrate layer being in direct contact with the first layer surface of the rubber layer.
9. The composite of claim 1, the rubber layer comprising a tread surface.
10. The composite of claim 1, the rubber layer being adjacent to a tread portion of a tire.
11. The composite of claim 1, the composite being a portion of a tire.
12. The composite of claim 11, the tire being a non-pneumatic tire.
13. The composite of claim 1, the polyurethane substrate comprising at least 90 weight percent of polyurethane.
14. The composite of claim 1, the rubber layer further comprising a reinforcing filler, the reinforcing filler being carbon black or silica.
15. The composite of claim 1, the rubber layer further comprising styrene butadiene rubber, polyisoprene rubber, polybutadiene rubber or natural rubber.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
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CN201780055542.0A CN109689356B (en) | 2016-07-28 | 2017-07-27 | Carbamate resins for polyurethane adhesives |
US16/320,544 US10919263B2 (en) | 2016-07-28 | 2017-07-27 | Carbamate resin for polyurethane adhesion |
EP17835263.9A EP3490794B1 (en) | 2016-07-28 | 2017-07-27 | Carbamate resin for polyurethane adhesion |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US201662367677P | 2016-07-28 | 2016-07-28 | |
US62/367,677 | 2016-07-28 |
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WO2018022876A1 true WO2018022876A1 (en) | 2018-02-01 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/US2017/044162 WO2018022876A1 (en) | 2016-07-28 | 2017-07-27 | Carbamate resin for polyurethane adhesion |
Country Status (4)
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US (1) | US10919263B2 (en) |
EP (1) | EP3490794B1 (en) |
CN (1) | CN109689356B (en) |
WO (1) | WO2018022876A1 (en) |
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JP7472568B2 (en) * | 2020-03-17 | 2024-04-23 | 住友ゴム工業株式会社 | Laminate, manufacturing method thereof, and airless tire |
CN112126396B (en) * | 2020-09-23 | 2023-03-17 | 湖北航泰科技有限公司 | Adhesive for improving adhesive property of heat insulating layer and lining, preparation method and use method thereof |
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Also Published As
Publication number | Publication date |
---|---|
EP3490794B1 (en) | 2021-09-08 |
CN109689356A (en) | 2019-04-26 |
US20190270276A1 (en) | 2019-09-05 |
CN109689356B (en) | 2021-07-02 |
EP3490794A4 (en) | 2020-03-18 |
US10919263B2 (en) | 2021-02-16 |
EP3490794A1 (en) | 2019-06-05 |
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