FR3067714A1 - Polybenzoxazine sulfuree utilisable pour le revetement de metal et son collage a du caoutchouc - Google Patents
Polybenzoxazine sulfuree utilisable pour le revetement de metal et son collage a du caoutchouc Download PDFInfo
- Publication number
- FR3067714A1 FR3067714A1 FR1755352A FR1755352A FR3067714A1 FR 3067714 A1 FR3067714 A1 FR 3067714A1 FR 1755352 A FR1755352 A FR 1755352A FR 1755352 A FR1755352 A FR 1755352A FR 3067714 A1 FR3067714 A1 FR 3067714A1
- Authority
- FR
- France
- Prior art keywords
- polybenzoxazine
- formula
- formulas
- substrate
- 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.)
- Withdrawn
Links
- 229920001971 elastomer Polymers 0.000 title claims abstract description 39
- 239000011248 coating agent Substances 0.000 title claims description 5
- 238000000576 coating method Methods 0.000 title claims description 5
- BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical group N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 claims abstract description 31
- 229910052751 metal Inorganic materials 0.000 claims abstract description 26
- 239000002184 metal Substances 0.000 claims abstract description 26
- 239000000758 substrate Substances 0.000 claims abstract description 19
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 17
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 15
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 15
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 12
- 125000003118 aryl group Chemical group 0.000 claims abstract description 11
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 10
- 125000005842 heteroatom Chemical group 0.000 claims abstract description 9
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 7
- 229910000975 Carbon steel Inorganic materials 0.000 claims abstract description 6
- 239000010962 carbon steel Substances 0.000 claims abstract description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 4
- 239000001257 hydrogen Substances 0.000 claims abstract description 4
- 125000001183 hydrocarbyl group Chemical group 0.000 claims abstract 2
- 229910000831 Steel Inorganic materials 0.000 claims description 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 9
- 239000010959 steel Substances 0.000 claims description 9
- 229910001369 Brass Inorganic materials 0.000 claims description 6
- 239000010951 brass Substances 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 3
- MUBKMWFYVHYZAI-UHFFFAOYSA-N [Al].[Cu].[Zn] Chemical compound [Al].[Cu].[Zn] MUBKMWFYVHYZAI-UHFFFAOYSA-N 0.000 claims description 2
- 229910045601 alloy Inorganic materials 0.000 claims description 2
- 239000000956 alloy Substances 0.000 claims description 2
- 150000002739 metals Chemical class 0.000 claims description 2
- 239000012790 adhesive layer Substances 0.000 abstract description 3
- 239000000178 monomer Substances 0.000 description 49
- 230000015572 biosynthetic process Effects 0.000 description 46
- 238000003786 synthesis reaction Methods 0.000 description 46
- 229920000642 polymer Polymers 0.000 description 39
- CMLFRMDBDNHMRA-UHFFFAOYSA-N 2h-1,2-benzoxazine Chemical compound C1=CC=C2C=CNOC2=C1 CMLFRMDBDNHMRA-UHFFFAOYSA-N 0.000 description 23
- 150000005130 benzoxazines Chemical class 0.000 description 18
- 239000000853 adhesive Substances 0.000 description 17
- 230000001070 adhesive effect Effects 0.000 description 17
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 14
- 150000004984 aromatic diamines Chemical class 0.000 description 13
- -1 benzoxazine compound Chemical class 0.000 description 13
- 150000001875 compounds Chemical class 0.000 description 13
- 239000000203 mixture Substances 0.000 description 13
- 150000001555 benzenes Chemical class 0.000 description 12
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 11
- 150000002989 phenols Chemical class 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 229940126214 compound 3 Drugs 0.000 description 7
- 239000010410 layer Substances 0.000 description 7
- 229920001187 thermosetting polymer Polymers 0.000 description 7
- TXDBDYPHJXUHEO-UHFFFAOYSA-N 2-methyl-4,6-bis(methylsulfanyl)benzene-1,3-diamine Chemical compound CSC1=CC(SC)=C(N)C(C)=C1N TXDBDYPHJXUHEO-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 229930040373 Paraformaldehyde Natural products 0.000 description 6
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
- 229940125782 compound 2 Drugs 0.000 description 6
- 229910052736 halogen Inorganic materials 0.000 description 6
- 125000004433 nitrogen atom Chemical group N* 0.000 description 6
- 229920002866 paraformaldehyde Polymers 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 5
- 150000001868 cobalt Chemical class 0.000 description 5
- 239000002131 composite material Substances 0.000 description 5
- 150000002367 halogens Chemical class 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 150000002430 hydrocarbons Chemical group 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 125000001424 substituent group Chemical group 0.000 description 5
- 239000011593 sulfur Substances 0.000 description 5
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 4
- 229910052794 bromium Inorganic materials 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 239000000806 elastomer Substances 0.000 description 4
- 230000008030 elimination Effects 0.000 description 4
- 238000003379 elimination reaction Methods 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 230000002787 reinforcement Effects 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 229920006395 saturated elastomer Polymers 0.000 description 4
- AOFIWCXMXPVSAZ-UHFFFAOYSA-N 4-methyl-2,6-bis(methylsulfanyl)benzene-1,3-diamine Chemical compound CSC1=CC(C)=C(N)C(SC)=C1N AOFIWCXMXPVSAZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 150000004985 diamines Chemical class 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 239000011159 matrix material Substances 0.000 description 3
- 230000001737 promoting effect Effects 0.000 description 3
- 239000012429 reaction media Substances 0.000 description 3
- 229910000029 sodium carbonate Inorganic materials 0.000 description 3
- 235000017550 sodium carbonate Nutrition 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000004753 textile Substances 0.000 description 3
- 150000003568 thioethers Chemical class 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- 229940125904 compound 1 Drugs 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- LHGVFZTZFXWLCP-UHFFFAOYSA-N guaiacol Chemical compound COC1=CC=CC=C1O LHGVFZTZFXWLCP-UHFFFAOYSA-N 0.000 description 2
- 210000003739 neck Anatomy 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 230000000306 recurrent effect Effects 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 238000007142 ring opening reaction Methods 0.000 description 2
- 229930195734 saturated hydrocarbon Natural products 0.000 description 2
- 150000003573 thiols Chemical class 0.000 description 2
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 2
- VWGKEVWFBOUAND-UHFFFAOYSA-N 4,4'-thiodiphenol Chemical compound C1=CC(O)=CC=C1SC1=CC=C(O)C=C1 VWGKEVWFBOUAND-UHFFFAOYSA-N 0.000 description 1
- GZFGOTFRPZRKDS-UHFFFAOYSA-N 4-bromophenol Chemical compound OC1=CC=C(Br)C=C1 GZFGOTFRPZRKDS-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229910001297 Zn alloy Inorganic materials 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 238000010533 azeotropic distillation Methods 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- PBAYDYUZOSNJGU-UHFFFAOYSA-N chelidonic acid Natural products OC(=O)C1=CC(=O)C=C(C(O)=O)O1 PBAYDYUZOSNJGU-UHFFFAOYSA-N 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 230000008094 contradictory effect Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- TVZPLCNGKSPOJA-UHFFFAOYSA-N copper zinc Chemical compound [Cu].[Zn] TVZPLCNGKSPOJA-UHFFFAOYSA-N 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 229920003244 diene elastomer Polymers 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 230000016507 interphase Effects 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical group [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000003507 refrigerant Substances 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 238000005987 sulfurization reaction Methods 0.000 description 1
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea group Chemical group NC(=S)N UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D171/00—Coating compositions based on polyethers obtained by reactions forming an ether link in the main chain; Coating compositions based on derivatives of such polymers
-
- 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
- B60C9/00—Reinforcements or ply arrangement of pneumatic tyres
- B60C9/0007—Reinforcements made of metallic elements, e.g. cords, yarns, filaments or fibres made from metal
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F136/00—Homopolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
- C08F136/02—Homopolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
- C08F136/04—Homopolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
- C08F136/14—Homopolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated containing elements other than carbon and hydrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
- C08G65/38—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols
- C08G65/40—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols from phenols (I) and other compounds (II), e.g. OH-Ar-OH + X-Ar-X, where X is halogen atom, i.e. leaving group
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D147/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds; Coating compositions based on derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D179/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen, with or without oxygen, or carbon only, not provided for in groups C09D161/00 - C09D177/00
- C09D179/02—Polyamines
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J147/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds; Adhesives based on derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J171/00—Adhesives based on polyethers obtained by reactions forming an ether link in the main chain; Adhesives based on derivatives of such polymers
-
- 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
- B60C9/00—Reinforcements or ply arrangement of pneumatic tyres
- B60C9/0007—Reinforcements made of metallic elements, e.g. cords, yarns, filaments or fibres made from metal
- B60C2009/0014—Surface treatments of steel cords
-
- 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
- B60C9/00—Reinforcements or ply arrangement of pneumatic tyres
- B60C9/0007—Reinforcements made of metallic elements, e.g. cords, yarns, filaments or fibres made from metal
- B60C2009/0021—Coating rubbers for steel cords
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Mechanical Engineering (AREA)
- Phenolic Resins Or Amino Resins (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Polyethers (AREA)
- Adhesives Or Adhesive Processes (AREA)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR1755352A FR3067714A1 (fr) | 2017-06-14 | 2017-06-14 | Polybenzoxazine sulfuree utilisable pour le revetement de metal et son collage a du caoutchouc |
| EP18737001.0A EP3638715B1 (fr) | 2017-06-14 | 2018-06-12 | Polybenzoxazine sulfuree utilisable pour le revetement de metal et son collage a du caoutchouc |
| PCT/FR2018/051368 WO2018229416A1 (fr) | 2017-06-14 | 2018-06-12 | Polybenzoxazine sulfuree utilisable pour le revetement de metal et son collage a du caoutchouc |
| JP2019569236A JP7365909B2 (ja) | 2017-06-14 | 2018-06-12 | 金属をコーティングするため、およびそれをゴムに接合するために使用することができる硫化ポリベンゾオキサジン |
| US16/621,520 US11624002B2 (en) | 2017-06-14 | 2018-06-12 | Sulfurized polybenzoxazine that can be used for coating metal and for the bonding of same to rubber |
| CN201880039502.1A CN110770279B (zh) | 2017-06-14 | 2018-06-12 | 可用于涂覆金属并用于该金属与橡胶的结合的硫化聚苯并噁嗪 |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR1755352A FR3067714A1 (fr) | 2017-06-14 | 2017-06-14 | Polybenzoxazine sulfuree utilisable pour le revetement de metal et son collage a du caoutchouc |
| FR1755352 | 2017-06-14 |
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| FR3067714A1 true FR3067714A1 (fr) | 2018-12-21 |
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| FR3057872A1 (fr) | 2016-10-26 | 2018-04-27 | Compagnie Generale Des Etablissements Michelin | Polybenzoxazine utilisable pour le revetement de metal et son collage a du caoutchouc |
| FR3057802A1 (fr) | 2016-10-26 | 2018-04-27 | Compagnie Generale Des Etablissements Michelin | Renfort metallique ou metallise dont la surface est revetue d'une polybenzoxazine |
| WO2018215700A1 (fr) | 2017-05-24 | 2018-11-29 | Compagnie Generale Des Etablissements Michelin | Benzoxazine halogénée utilisable pour la synthèse de polybenzoxazine |
| WO2018215701A1 (fr) | 2017-05-24 | 2018-11-29 | Compagnie Generale Des Etablissements Michelin | Benzoxazine halogénée utilisable pour la synthèse de polybenzoxazine |
| FR3067029A1 (fr) | 2017-05-31 | 2018-12-07 | Compagnie Generale Des Etablissements Michelin | Benzoxazine boree utilisable pour la synthese de polybenzoxazine |
| FR3067646A1 (fr) | 2017-06-14 | 2018-12-21 | Compagnie Generale Des Etablissements Michelin | Renfort metallique ou metallise dont la surface est revetue d'une polybenzoxazine sulfuree |
| FR3067713A1 (fr) | 2017-06-14 | 2018-12-21 | Compagnie Generale Des Etablissements Michelin | Benzoxazine sulfuree utilisable pour la synthese d'une polybenzoxazine |
| FR3089228A3 (fr) | 2018-11-30 | 2020-06-05 | Michelin & Cie | Collage d’un monobrin en composite verre-résine à une matrice thermoplastique |
| FR3089217A3 (fr) | 2018-11-30 | 2020-06-05 | Michelin & Cie | Matériau multi-composite à base de composite verre-résine |
| EP3888940B1 (en) | 2020-04-01 | 2023-01-11 | The Goodyear Tire & Rubber Company | A rubber composition and a rubber product |
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| WO2014063968A1 (fr) * | 2012-10-24 | 2014-05-01 | Compagnie Generale Des Etablissements Michelin | Polyamine polyaromatique soufree utilisable pour la synthese de polyuree |
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| US5543516A (en) | 1994-05-18 | 1996-08-06 | Edison Polymer Innovation Corporation | Process for preparation of benzoxazine compounds in solventless systems |
| US20030023007A1 (en) | 2001-07-27 | 2003-01-30 | Hycomp, Inc. | Enhancement of thermal properties of benzoxazine polymers by use of aromatic polyamines to incorporate internal benzoxazine groups within the monomer |
| US7649060B2 (en) | 2005-12-02 | 2010-01-19 | Henkel Corporation | Curable compositions |
| JP4102853B2 (ja) | 2005-09-29 | 2008-06-18 | 積水化学工業株式会社 | 熱硬化性樹脂、及びそれを含む熱硬化性組成物、並びにそれから得られる成形体 |
| US8227390B2 (en) | 2007-11-28 | 2012-07-24 | Akebono Brake Industry Co., Ltd. | Binder resin for friction material, binder resin composition for friction material, composite material for friction material containing the same, friction material and production method thereof |
| WO2010002872A2 (en) * | 2008-06-30 | 2010-01-07 | Henkel Corporation | High performance adhesives and methods of their use |
| JP2011016787A (ja) | 2009-06-08 | 2011-01-27 | Toyohashi Univ Of Technology | 液晶性ベンゾオキサジン系化合物及び液晶性ベンゾオキサジン系重合組成物 |
| JP2010265480A (ja) | 2010-08-04 | 2010-11-25 | Hitachi Chem Co Ltd | 新規な熱硬化性ベンゾオキサジン樹脂、その製造法及び硬化物 |
| WO2012135180A1 (en) | 2011-03-28 | 2012-10-04 | 3M Innovative Properties Company | Curable composition, article, method of curing, and tack-free reaction product |
| FR2978769B1 (fr) | 2011-08-04 | 2013-09-27 | Michelin Soc Tech | Composition adhesive aqueuse a base de polyaldehyde et de polyphenol |
| FR2978771B1 (fr) | 2011-08-04 | 2013-09-27 | Michelin Soc Tech | Composition adhesive aqueuse a base de polyaldehyde et 2,2', 4,4'-tetrahydroxydiphenyl sulfide |
| FR2978770B1 (fr) | 2011-08-04 | 2013-09-27 | Michelin Soc Tech | Composition adhesive aqueuse a base de polyaldehyde et phloroglucinol |
| JP2013043950A (ja) | 2011-08-25 | 2013-03-04 | Gun Ei Chem Ind Co Ltd | 低誘電材料用熱硬化性樹脂 |
| GB201205574D0 (en) | 2012-03-29 | 2012-05-16 | Cytec Tech Corp | Benzoxazines and compositions containing the same |
| KR102103396B1 (ko) | 2012-10-24 | 2020-04-22 | 꽁빠니 제네날 드 에따블리세망 미쉘린 | 금속을 고무에 접착시키기 위한 접착 프라이머로서 특히 유용한 폴리우레아 |
| FR3005050A1 (fr) | 2013-04-26 | 2014-10-31 | Michelin & Cie | Compose polyol soufre utilisable comme monomere pour la synthese de polyurethane |
| FR3005054B1 (fr) | 2013-04-26 | 2016-07-01 | Michelin & Cie | Polymere utilisable notamment comme primaire d'adhesion pour le collage de metal a du caoutchouc |
| FR3008707B1 (fr) | 2013-07-16 | 2017-11-10 | Michelin & Cie | Composition adhesive aqueuse a base d'aldehyde biosource et de polyphenol |
| TWI573820B (zh) * | 2014-06-30 | 2017-03-11 | 可隆股份有限公司 | 聚氧代氮代苯并環己烷前驅物及其製備方法 |
| US20170327973A1 (en) | 2014-12-03 | 2017-11-16 | National Institute Of Advanced Industrial Science And Technology | Carbon-Fiber Precursor Fiber, Carbon Fiber, and Method for Producing Carbon Fiber |
| JP2016124980A (ja) | 2014-12-27 | 2016-07-11 | 三星電子株式会社Ｓａｍｓｕｎｇ Ｅｌｅｃｔｒｏｎｉｃｓ Ｃｏ．，Ｌｔｄ． | 接着剤 |
| FR3045457B1 (fr) | 2015-12-16 | 2017-12-15 | Michelin & Cie | Renfort metallique ou metallise dont la surface est revetue d’une polybenzoxazine |
| FR3045619B1 (fr) * | 2015-12-16 | 2017-12-15 | Michelin & Cie | Polybenzoxazine utilisable pour le revetement de metal et son collage a du caoutchouc |
| FR3057872A1 (fr) | 2016-10-26 | 2018-04-27 | Compagnie Generale Des Etablissements Michelin | Polybenzoxazine utilisable pour le revetement de metal et son collage a du caoutchouc |
| FR3057802A1 (fr) | 2016-10-26 | 2018-04-27 | Compagnie Generale Des Etablissements Michelin | Renfort metallique ou metallise dont la surface est revetue d'une polybenzoxazine |
| WO2018215700A1 (fr) | 2017-05-24 | 2018-11-29 | Compagnie Generale Des Etablissements Michelin | Benzoxazine halogénée utilisable pour la synthèse de polybenzoxazine |
| WO2018215701A1 (fr) | 2017-05-24 | 2018-11-29 | Compagnie Generale Des Etablissements Michelin | Benzoxazine halogénée utilisable pour la synthèse de polybenzoxazine |
| FR3067029A1 (fr) | 2017-05-31 | 2018-12-07 | Compagnie Generale Des Etablissements Michelin | Benzoxazine boree utilisable pour la synthese de polybenzoxazine |
| FR3067646A1 (fr) | 2017-06-14 | 2018-12-21 | Compagnie Generale Des Etablissements Michelin | Renfort metallique ou metallise dont la surface est revetue d'une polybenzoxazine sulfuree |
| FR3067713A1 (fr) | 2017-06-14 | 2018-12-21 | Compagnie Generale Des Etablissements Michelin | Benzoxazine sulfuree utilisable pour la synthese d'une polybenzoxazine |
-
2017
- 2017-06-14 FR FR1755352A patent/FR3067714A1/fr not_active Withdrawn
-
2018
- 2018-06-12 WO PCT/FR2018/051368 patent/WO2018229416A1/fr not_active Ceased
- 2018-06-12 US US16/621,520 patent/US11624002B2/en active Active
- 2018-06-12 CN CN201880039502.1A patent/CN110770279B/zh active Active
- 2018-06-12 EP EP18737001.0A patent/EP3638715B1/fr active Active
- 2018-06-12 JP JP2019569236A patent/JP7365909B2/ja active Active
Patent Citations (1)
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|---|---|---|---|---|
| WO2014063968A1 (fr) * | 2012-10-24 | 2014-05-01 | Compagnie Generale Des Etablissements Michelin | Polyamine polyaromatique soufree utilisable pour la synthese de polyuree |
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| POORTEMAN MARC ET AL: "Thermal curing ofpara-phenylenediamine benzoxazine for barrier coating applications on 1050 aluminum alloys", PROGRESS IN ORGANIC COATINGS, ELSEVIER BV, NL, vol. 97, 8 April 2016 (2016-04-08), pages 99 - 109, XP029557542, ISSN: 0300-9440, DOI: 10.1016/J.PORGCOAT.2016.03.026 * |
Also Published As
| Publication number | Publication date |
|---|---|
| CN110770279B (zh) | 2022-09-16 |
| US11624002B2 (en) | 2023-04-11 |
| JP7365909B2 (ja) | 2023-10-20 |
| CN110770279A (zh) | 2020-02-07 |
| JP2020523459A (ja) | 2020-08-06 |
| EP3638715B1 (fr) | 2023-08-23 |
| EP3638715A1 (fr) | 2020-04-22 |
| US20200095458A1 (en) | 2020-03-26 |
| WO2018229416A1 (fr) | 2018-12-20 |
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