WO2001094493A2 - Epoxy based reinforcing patches with improved adhesion to oily metal surfaces - Google Patents
Epoxy based reinforcing patches with improved adhesion to oily metal surfaces Download PDFInfo
- Publication number
- WO2001094493A2 WO2001094493A2 PCT/US2001/017562 US0117562W WO0194493A2 WO 2001094493 A2 WO2001094493 A2 WO 2001094493A2 US 0117562 W US0117562 W US 0117562W WO 0194493 A2 WO0194493 A2 WO 0194493A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- thermosetting adhesive
- reinforcing sheet
- rubber
- percent
- conjugated diene
- Prior art date
Links
- 230000003014 reinforcing effect Effects 0.000 title claims abstract description 56
- 229910052751 metal Inorganic materials 0.000 title description 5
- 239000002184 metal Substances 0.000 title description 5
- 239000004593 Epoxy Substances 0.000 title description 3
- 229920001971 elastomer Polymers 0.000 claims abstract description 43
- 239000005060 rubber Substances 0.000 claims abstract description 43
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 39
- 239000003822 epoxy resin Substances 0.000 claims abstract description 32
- 239000000758 substrate Substances 0.000 claims abstract description 26
- 150000002825 nitriles Chemical class 0.000 claims abstract description 20
- 239000000178 monomer Substances 0.000 claims abstract description 18
- 239000000853 adhesive Substances 0.000 claims description 66
- 230000001070 adhesive effect Effects 0.000 claims description 66
- 229920001187 thermosetting polymer Polymers 0.000 claims description 58
- 229920000459 Nitrile rubber Polymers 0.000 claims description 28
- 150000001993 dienes Chemical class 0.000 claims description 24
- 239000003795 chemical substances by application Substances 0.000 claims description 16
- 229920003244 diene elastomer Polymers 0.000 claims description 16
- 239000004005 microsphere Substances 0.000 claims description 16
- 239000007787 solid Substances 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 13
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical group NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 claims description 10
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 9
- 239000012779 reinforcing material Substances 0.000 claims description 8
- 239000011888 foil Substances 0.000 claims description 6
- 239000004604 Blowing Agent Substances 0.000 claims description 5
- 229910052782 aluminium Inorganic materials 0.000 claims description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 4
- 229930185605 Bisphenol Natural products 0.000 claims description 3
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 claims description 3
- 239000003973 paint Substances 0.000 claims description 3
- 239000002759 woven fabric Substances 0.000 claims description 3
- 239000012790 adhesive layer Substances 0.000 abstract description 9
- 229920013646 Hycar Polymers 0.000 description 33
- 239000010410 layer Substances 0.000 description 19
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 18
- KUBDPQJOLOUJRM-UHFFFAOYSA-N 2-(chloromethyl)oxirane;4-[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical compound ClCC1CO1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 KUBDPQJOLOUJRM-UHFFFAOYSA-N 0.000 description 15
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 14
- 239000000203 mixture Substances 0.000 description 10
- 239000003054 catalyst Substances 0.000 description 8
- 239000004927 clay Substances 0.000 description 8
- 239000011521 glass Substances 0.000 description 8
- 230000009477 glass transition Effects 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 239000002994 raw material Substances 0.000 description 6
- -1 amine salts Chemical class 0.000 description 5
- 229910000831 Steel Inorganic materials 0.000 description 4
- NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 239000010959 steel Substances 0.000 description 4
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 4
- 230000004888 barrier function Effects 0.000 description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 230000002787 reinforcement Effects 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical class P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000011152 fibreglass Substances 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 239000010881 fly ash Substances 0.000 description 2
- 239000002346 layers by function Substances 0.000 description 2
- 239000004850 liquid epoxy resins (LERs) Substances 0.000 description 2
- 150000002924 oxiranes Chemical class 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 229920002587 poly(1,3-butadiene) polymer Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 238000000518 rheometry Methods 0.000 description 2
- 239000003981 vehicle Substances 0.000 description 2
- ZWOULFZCQXICLZ-UHFFFAOYSA-N 1,3-dimethyl-1-phenylurea Chemical compound CNC(=O)N(C)C1=CC=CC=C1 ZWOULFZCQXICLZ-UHFFFAOYSA-N 0.000 description 1
- 229920002799 BoPET Polymers 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 239000005041 Mylar™ Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical class OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002318 adhesion promoter Substances 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical class OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 1
- 235000019399 azodicarbonamide Nutrition 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 150000001558 benzoic acid derivatives Chemical class 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 230000001413 cellular effect Effects 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000002666 chemical blowing agent Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- 229920006332 epoxy adhesive Polymers 0.000 description 1
- 230000005294 ferromagnetic effect Effects 0.000 description 1
- 229910021485 fumed silica Inorganic materials 0.000 description 1
- 230000008570 general process Effects 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 239000006249 magnetic particle Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- 229910000073 phosphorus hydride Chemical class 0.000 description 1
- 125000005498 phthalate group Chemical class 0.000 description 1
- 239000008029 phthalate plasticizer Substances 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
Classifications
-
- 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
- C09J163/00—Adhesives based on epoxy resins; Adhesives based on derivatives of epoxy resins
-
- 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
- C09J7/00—Adhesives in the form of films or foils
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
- C09J7/21—Paper; Textile fabrics
-
- 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
- C09J7/00—Adhesives in the form of films or foils
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
- C09J7/22—Plastics; Metallised plastics
-
- 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
- C09J7/00—Adhesives in the form of films or foils
- C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
- C09J7/35—Heat-activated
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2207/00—Foams characterised by their intended use
- C08J2207/02—Adhesive
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
- C08L2666/04—Macromolecular compounds according to groups C08L7/00 - C08L49/00, or C08L55/00 - C08L57/00; Derivatives thereof
- C08L2666/08—Homopolymers or copolymers according to C08L7/00 - C08L21/00; Derivatives thereof
-
- 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
- C09J2433/00—Presence of (meth)acrylic polymer
-
- 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
- C09J2463/00—Presence of epoxy resin
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/14—Layer or component removable to expose adhesive
- Y10T428/1405—Capsule or particulate matter containing [e.g., sphere, flake, microballoon, etc.]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/23—Sheet including cover or casing
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24802—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.]
- Y10T428/24843—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.] with heat sealable or heat releasable adhesive layer
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/249921—Web or sheet containing structurally defined element or component
- Y10T428/249924—Noninterengaged fiber-containing paper-free web or sheet which is not of specified porosity
- Y10T428/24994—Fiber embedded in or on the surface of a polymeric matrix
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/249921—Web or sheet containing structurally defined element or component
- Y10T428/249953—Composite having voids in a component [e.g., porous, cellular, etc.]
- Y10T428/249955—Void-containing component partially impregnated with adjacent component
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer
- Y10T428/2813—Heat or solvent activated or sealable
Definitions
- This invention relates to reinforcing sheets such as those adapted for applying localized reinforcement to sheet metal or sheet plastic structures.
- these reinforcing sheets include one or more layers of a stiffening material and one or more layers of a polymeric material that acts as a binder for the stiffening material as well as an adhesive for securing the reinforcing sheet to a substrate.
- a polymeric material that acts as a binder for the stiffening material as well as an adhesive for securing the reinforcing sheet to a substrate.
- protective foils, moisture barriers and other layers may be included in the reinforcing sheet.
- a common adhesive for these reinforcing sheets is described in U. S. Patent
- That adhesive includes a mixture of an epoxy resin, a curing agent and a carboxy-terminated butadiene-acrylonitrile rubber.
- the butadiene-acrylonitrile rubber commonly used contains 18 weight percent or more polymerized acrylonitrile, has a glass transition temperature of -52°C or higher and has a solubility parameter, as reported by its manufacturer, of 8.82 or above.
- the amount of the butadiene-acrylonitrile rubber is such that the adhesive as a whole contains 4 percent or more by weight polymerized acrylonitrile.
- the rubber is typically pre-reacted with a portion of the epoxy resin before being formulated into the adhesive mixture. The rubber imparts a certain amount of toughness to the adhesive once it is cured.
- these reinforcing sheets are typically applied to exterior body panels. Because the epoxy resin in these reinforcing sheets must be cured, the reinforcing sheets are usually applied before the body panel is painted, so that the epoxy resin and paint can be cured simultaneously. Often, the unpainted body panel (or other substrate) is contaminated with oily materials. In other cases, the substrate is cold for one reason or another when the reinforcing sheet is applied.
- the epoxy adhesive commonly used in the reinforcing sheets does not adhere well to oily or cold surfaces. When these conditions are present, the manufacturer either accepts that a certain amount of reinforcing sheets will be poorly adhered, or else the substrate parts must be warmed and/or cleaned before applying the reinforcing sheet. Neither of these options is attractive. Warming and cleaning the substrate introduce extra steps into the process of assembling a vehicle. This in turn imposes extra costs for time, energy and handling. It would be desirable to provide a reinforcing sheet that adheres better to oily or cold substrates.
- thermosetting adhesive includes (a) a curing agent and (b) an epoxy-terminated adduct of an epoxy resin and a conjugated diene or conjugated diene/nitrile rubber containing not more than 15 percent by weight polymerized nitrile monomer, and wherein said thermosetting adhesive contains no more than 3.5 percent by weight polymerized nitrile monomer.
- the reinforcing sheet of the invention adheres well to oily substrates as well as to colder substrates, compared to otherwise similar reinforcing sheets in which the nitrile monomer content in the thermosetting adhesive layer is somewhat higher.
- this invention is a method of reinforcing a substrate, comprising
- thermosetting adhesive includes (a) a curing agent and (b) an epoxy-terminated adduct of an epoxy resin and a conjugated diene or conjugated diene/nitrile rubber containing not more than 15 percent by weight polymerized nitrile monomer, and wherein said thermosetting adhesive contains no more than 3.5 percent by weight polymerized nitrile monomer, and then
- thermosetting adhesive (B) curing said thermosetting adhesive.
- thermosetting adhesive layer of the invention includes an epoxy- terminated adduct of an epoxy resin and a diene rubber or a conjugated diene/nitrile rubber having containing not more than 15 percent by weight polymerized nitrile monomer.
- This adduct is suitably prepared in the reaction of a polyepoxide with a carboxy-functional conjugated diene rubber or a conjugated diene/nitrile rubber.
- the diene rubber is a polymer of a conjugated diene monomer such as butadiene and isoprene. Butadiene rubbers are preferred. Conjugated diene/nitrile rubbers are copolymers of a conjugated diene and an ethylenically unsaturated nitrile monomer, of which acrylonitrile is the most preferred one. When a conjugated diene/nitrile rubber is used, at least one such rubber present in the composition contains less than 15 weight percent polymerized unsaturated nitrile, and preferably no more than 12 weight percent polymerized unsaturated nitrile. The rubber also contains terminal groups that will react with an epoxide to form a covalent bond thereto. Preferably, the rubber contains from 1.5, more preferably from 1.8, to 2.5, more preferably to 2.2, of such terminal groups per molecule, on average. Carboxyl-terminated rubbers are preferred.
- the rubber is preferably a liquid at room temperature, and preferably has a glass transition temperature of less than -55°C, preferably from -60 to -90°C.
- the molecular weight (M ⁇ ) of the rubber is suitably 2000 to 6000, more preferably from 3000 to 5000.
- Suitable carboxyl-functional butadiene and butadiene/acrylonitrile rubbers are commercially available from B. F. Goodrich under the trade names Hycar® 2000X162 carboxyl-terminated butadiene homopolymer and Hycar® 1300X31 carboxyl-terminated butadiene/acrylonitrile copolymer.
- a suitable amine-terminated butadiene/acrylonitrile copolymer is sold under the tradename Hycar® 1300X21.
- a conjugated diene or conjugated diene/nitrile rubber having a somewhat higher polymerized nitrile content can be used in addition to the rubber described above.
- Higher acrylonitrile content provides better adhesion between the polymer and some substrates such as glass, and tends to increase flexural strength somewhat.
- the high nitrile rubber also preferably contains terminal epoxy-reactive groups.
- the high nitrile rubber advantageously contains from above 15 percent, more preferably at least 18 percent to 40 percent, more preferably to 32 percent polymerized nitrile monomer.
- the high nitrile rubber suitably has a molecular weight of 3000 to 6000, and contains from 1.5 more preferably from 1.8, to 2.5, more preferably to 2.2, epoxy- reactive terminal groups per molecule, on average.
- Examples of such high nitrile rubbers are Hycar® 1300X8, Hycar® 1300X13®, Hycar® 1300X9 and Hycar® 1300X18 carboxyl- terminated butadiene acrylonitrile copolymers, all commercially available from B. F. Goodrich.
- the rubbers (that is, the conjugated diene or conjugated diene/nitrile rubber, plus the high nitrile rubber, if used) are present in an amount such that the thermosetting composition contains no more than 3.5 percent polymerized nitrile monomer. It is more preferred that the thermosetting adhesive contains from 1 to 3.25 percent by weight polymerized nitrile monomer. Preferably, the rubbers constitute from 5, more preferably from 10, to 40, more preferably to 25 percent of the total weight of the thermosetting adhesive.
- the high nitrile rubber preferably constitutes no more than 50, preferably no more than 45 percent, more preferably no more than 35 percent of the combined weight of all rubbers.
- the conjugated diene or conjugated diene/nitrile rubber is formed into an epoxy-terminated adduct by reaction with an excess of a polyepoxide. Any high nitrile rubber that is used is similarly converted into an epoxy-terminated adduct.
- polyepoxide compounds such as cycloaliphatic epoxides, epoxidized novolac resins, epoxidized bisphenol A or bisphenol F resins, butanediol polyglycidyl ether, neopentyl glycol polyglycidyl ether or flexibilizing epoxy resins can be used, but generally preferred on the basis of cost and availability are liquid or solid glycidyl ethers of a bisphenol such as bisphenol A or bisphenol F.
- Halogenated, particularly brominated, resins can be used to impart flame retardant properties if desired.
- liquid epoxy resins such as DER 331, available from The Dow Chemical Company
- DER 331 available from The Dow Chemical Company
- the rubber and an excess of the polyepoxide are mixed together with a polymerization catalyst such as a substituted urea or phosphine catalyst, and heated to a temperature of 100-250°C in order to form the adduct.
- Preferred catalysts include phenyl dimethyl urea and triphenyl phosphine.
- enough of the polyepoxide compound is used that the resulting product is a mixture of the adduct and free polyepoxide compound.
- the adduct is not a solid at room temperature 28°F (-2.22°C), it is suitably blended with a normally solid (at room temperature) epoxy resin.
- a normally solid epoxy resin is a polyglycidyl ether of bisphenol A or bisphenol F having an epoxy equivalent weight of 300 to 1000. Enough of the solid epoxy resin is blended with the adduct so the resulting mixture is solid at room temperature.
- thermosetting adhesive also contains a curing agent.
- curing agents A large number of curing agents are useful, particularly those that require elevated temperatures (that is, above 50°C) to cure.
- Lewis acids, substituted imidazoles or amine salts can be used as curing agents.
- Blocked amine curing agents such as those made by the reaction of approximately equimolar amounts of an anhydride and a polyamine are also useful. Such blocked amine curing agents are described in U. S. Patent Number 4,766,183.
- An especially useful curing agent is dicyandiamide.
- the curing agent is used in amounts sufficient to provide a complete cure, such as 0.25 to 10, preferably 2 to 5 percent of the weight of the thermosetting adhesive.
- the thermosetting adhesive preferably is cellular when fully cured and/or contains a quantity of microspheres in order to reduce density.
- Suitable microspheres include those made from inorganic materials such as glass and silica-alumina ceramics or polymeric materials such as epoxy resin, unsaturated polyester resin, silicone resin, phenolics, polyvinyl alcohol, polyvinyl chloride, polypropylene, and polystyrene.
- fly ash that is in the form of hollow particles can be used. Examples of commercially available fly ash of this type is sold by Boliden Intertrade, Inc., under the trade names Fillite 100 and Fillite 150. Glass microspheres are most preferred.
- microspheres most advantageously have average diameters of from 5 to 150 microns, preferably from 20 to 85 microns.
- the microspheres advantageously have a bulk density of from 0.1 to 0.5 g/cc.
- the microspheres may be surface treated with an interfacial adhesion promoter such as a silane compound.
- Microspheres preferably constitute from 5, more preferably from 10, to 30, more preferably to 20 percent of the total weight of the thermosetting adhesive.
- thermosetting adhesive may also contain a blowing agent that becomes activated at the curing temperature to expand the adhesive layer.
- Suitable blowing agents include physical blowing agents such as hydrocarbons, hydrofluorocarbons, hydrochlorofluorocarbons, but more preferably include chemical blowing agents such as azobisformamide.
- thermosetting adhesive may contain one or more other fillers or rheology control agents.
- suitable fillers include talcs, clays, silicas, calcium carbonate, graphite, glass, carbon black, plastic powders such as ABS. Magnetic particles such as ferromagnetic particles may be used as a filler, as well.
- Suitable rheology control agents include fumed silica and certain clays such as bentonite clay and montmorillonite clay.
- the thermosetting adhesive can include a plasticizer for impact and thermal shock resistance improvement.
- a plasticizer for impact and thermal shock resistance improvement can be used as the plasticizer.
- benzoates, adipates, terephthalates and phthalates can be used as the plasticizer.
- thermosetting adhesive can further contain a flame retardant, such as hydrated alumina or antimony oxide.
- thermosetting adhesive is preferably formulated to be tacky at a temperature of 15° to 40°C.
- the thermosetting adhesive is applied to at least one side of a reinforcing layer.
- the reinforcing layer is preferably made of a stiff yet flexible construction, in order to provide reinforcement when applied to a substrate, and yet conform to the shape of the substrate.
- Preferred reinforcing materials are fibers of stiff materials such as glass, polyamide resin, polypropylene resin and carbon, as well as aluminum sheet or foil, films of high melting thermoplastic resins such as Mylar, that may be fiber-reinforced. More preferred reinforcing materials are woven fabrics of stiff fibers as just described, especially woven glass fabrics. Mixtures of two or more different fibers can be woven together if desired. For example, carbon fibers may be woven into a glass fabric to increase stiffness at a moderate cost.
- the reinforcing layer preferably has a thickness of 0.003 inch to 0.050 inch (.0762-1.27 mm).
- the reinforcing layer may have a planar and/or smooth configuration, or may include three-dimensional features to further increase stiffness and/or adapt the reinforcing sheet for a particular application.
- the reinforcing layer may have a ribbed configuration such as is described in Figures 3-5 of U.S. Patent Number 4,803,105.
- Another suitable reinforcing layer is a honeycomb structure as described in U.S. Patent Number 4,803,108. These honeycomb structures include a perforated honeycomb member having columns that define cell apertures with open ends.
- the honeycomb structure is suitably formed of any material that remains stable up to the curing temperature of the thermosetting adhesive and exhibits sufficient adhesion to the thermosetting adhesive layer and sufficient flexibility to conform to the shape of the panel to be reinforced.
- the honeycomb structure is formed of a metal alloy plate. Because of its light weight, corrosion resistance, ready accessibility, inexpensive cost and high flexibility, aluminum is most preferred for forming the honeycomb structure.
- the columns of the honeycomb structure are integrally connected to form a multitude of cell apertures with open ends .
- the cells of the honeycomb structure may be hexagonal, triangular, square, polyhedral or other convenient shapes .
- the columns of the honeycomb structure are sufficiently thick, and the cell apertures defined by the columns have a suitable cell size and core density, such that the honeycomb structure maintains its integrity while maintaining the capability to conform to the shape of the substrate and without unacceptably increasing the weight of the reinforcing sheet .
- the preferred aluminum honeycomb columns suitably have a thickness of 0.0005 inch to 0.005 inch (0.013-0.13 mm, preferably 0.0007 inch to 0.004 inch (0.0018-0.1 mm) .
- the cell apertures suitably have a cell size of 1/16 inch to 7/8 inch (1.6-22.2 mm), preferably 3/16 inch to 5/16 inch (4.8-8.0 mm), and a core density of 1.0 pound per cubic foot to 12.0 pounds per cubic foot (1.6-19.2 kg/m 3 ), preferably 3.0 pounds per cubic foot to 8.0 pounds per cubic foot (4.8-12.8 kg/m 3 ) .
- the honeycomb member suitably has a thickness of 1/16 inch to 4 inches (1.6-102 mm), preferably 1/8 inch to 3/4 inch (3.2-19 mm).
- the reinforcing sheet may contain one or more additional functional layers, such as a moisture barrier layer as described in U. S. Patent Number 4,803,105.
- a moisture barrier layer as described in U. S. Patent Number 4,803,105.
- Another useful functional layer is a release sheet, typically paper, which covers the exposed surface of the adhesive layer that is brought into contact with the substrate to be reinforced.
- a slit, heat-shrinkable protection foil of the type described in U. S. Patent Number 4,900,601 can be used on the surface of the adhesive layer.
- the reinforcing sheet advantageously is prepared by applying a layer of the thermosetting adhesive to the reinforcing layer.
- a convenient way of accomplishing this is to spread a layer of the thermosetting adhesive onto a release layer or protection foil with a coating knife to a uniform thickness suitably of 0.01 inch to 0.10 inch (0.25-2.5 mm), preferably 0.02 inch to 0.05 inch (0.5-1.25 mm).
- the reinforcing layer is then placed on the thermosetting adhesive layer and pressed in with a pressure roll.
- the entire reinforcing sheet is then pressed with a roller to provide a sheet with total thickness suitably of 0.03 inch to 0.30 inch (0.75-7.5 mm), preferably 0.04 inch to 0.10 inch (1.0-2.5 mm).
- the exposed surface of the thermosetting adhesive layer is brought in contact with the panel.
- An advantage of the reinforcing sheet of this invention is that it adheres well to substrates that are somewhat oily or somewhat cold.
- the reinforcing sheet is of particular interest when applied to a substrate that is at a temperature of from 15°C to 40°C, preferably from 12°C to 35°C.
- the reinforcing sheet of the invention exhibits substantially improved adhesion to substrates at temperatures of 15 °C to 22° C, compared to previous reinforcing sheets in which the thermosetting adhesive contained only a high nitrile rubber.
- the substrate and applied reinforcing sheet are subsequently heated to cure the thermosetting adhesive. This is conveniently done at a temperature of from 150°C to 200°C, for a period of 15 minutes to 1 hour. This curing step can be done simultaneously with other treatments requiring heating, such as curing paints or E-coats.
- An epoxy-terminated adduct was prepared by blending 59.85 parts of a liquid epoxy resin (DER 331, from The Dow Chemical Company), 0.33 part of triphenyl phosphine, 22.86 parts of Hycar® 1300X31 butadiene/acrylonitrile rubber and 16.96 parts of Hycar® 1300X18 butadiene/acrylonitrile rubber.
- Hycar® 1300X31 rubber was a carboxyl-terminated, 3800 M n polymer containing 10 percent by weight polymerized acrylonitrile.
- Hycar® 1300X31 rubber had a glass transition temperature of -66°C and a calculated solubility parameter of 8.46
- Hycar® 1300X18 rubber was a carboxyl-terminated, 3400 M n copolymer containing 21.5 percent polymerized acrylonitrile. As reported by the manufacturer, it had a glass transition temperature of -46°C and a solubility parameter of 8.99.
- the blended mixture was heated to 100°C for 3 hours to form the desired epoxy-terminated adduct.
- the epoxy-terminated adduct (70.23 parts) was then blended with 29.77 parts of a solid epoxy resin, DER 661, sold by The Dow Chemical Company. A portion of the resulting blend (75.7 parts) was mixed with 4.3 parts dicyandiamide, 6 parts of a clay filler and 14 parts of glass microspheres (K25, sold by 3M Corporation) to form Thermosetting Adhesive 1.
- Thermosetting Adhesive 1 contained 3.1 percent polymerized acrylonitrile.
- Thermosetting Adhesive 2 was made in the same general way as described in Example 1, except that Hycar® 1300X31 was the only rubber used.
- the overall proportions of raw materials (exclusive of catalysts) were:
- the acrylonitrile content of Thermosetting Adhesive 2 was 2.2 percent by weight.
- Comparative Adhesive A was made in the same general process as described in Example 1, except that the only rubber used was Hycar® 1300X8.
- Hycar® 1300X8 was reported by its manufacturer to have an acrylonitrile content of 18 percent by weight, a molecular weight (M n ) of 3550, an average carboxyl functionality of 1.8 and a glass transition temperature of -52°C.
- the overall proportions of raw materials (exclusive of catalysts) were:
- Comparative Adhesive A The acrylonitrile content of Comparative Adhesive A is 4 percent by weight.
- the tack of Thermosetting Adhesive 2 was evaluated in the following manner: Multiple patch samples were prepared by applying a 1 X 6 inch (2.5 X 15 cm) piece of Hexcel-Schwebel 7544 woven fiberglass mat over the adhesive to form patches having a total thickness of 1.3 mm. The patches were then applied to oily pieces of steel having dimensions of 4 X 6 inches (10 X 15 cm) and a thickness of 0.03 i inch (0.79 mm). The steel was at a temperature of 70°F (21°C). A force of 4.5 lb (20 N) is applied to the patch against the steel to simulate application of the patch by hand as in a vehicle assembly plant. The patch was then allowed to "wet out" for varying periods at 70°F (21°C). The adhesion of the patch is evaluated on an Instron tensile test machine.
- Thermosetting Adhesive 2 exhibited a peel strength at 70°F (21°) that was at least 250 percent that of Comparative Adhesive A at the same temperature.
- the peel strengths of Thermosetting Adhesive 2 were reduced, compared to the values at 70°F (21°C), thus illustrating the effect of substrate temperatures on adhesion.
- the values for Thermosetting Adhesive 2 at 50°F (10°C) were still much greater than those of Comparative Adhesive A at 70°F (21 °C).
- Thermosetting Adhesive 3 was made in the same general way as described in Example 1, except that the rubbers used were Hycar® 1300X31 and Hycar® 1300X8.
- the overall proportions of raw materials (exclusive of catalysts) were:
- Hycar® 1300X31 rubber 18.1 parts
- the acrylonitrile content of Thermosetting Adhesive 3 is 2.4 percent by weight.
- Thermosetting Adhesive 4 was made in the same general way as described in Example 1, except that the rubbers used were Hycar® 1300X31 and Hycar® 1300X13. Hycar®. 1300X13 was reported by its manufacturer to have an acrylonitrile content of 26 percent by weight, a molecular weight (M n ) of 3150, an average carboxyl functionality of 1.8 and a glass transition temperature of -39°C.
- the overall proportions of raw materials (exclusive of catalysts) were:
- the acrylonitrile content of the Thermosetting Adhesive 4 is 3.5 percent by weight.
- Thermosetting Adhesive 5 was made in the same general way as described in Example 3, with different proportions of ingredients.
- the overall proportions of raw materials were: DER 331 epoxy resin 31.9 parts
- Hycar® 1300X31 rubber 18.1 parts
- Hycar® 1300X8 rubber 3.1 parts
- the acrylonitrile content of Thermosetting Adhesive 5 is 2.6 percent by weight.
- Thermosetting Adhesives 3-5 were used to form duplicate patch samples by applying a 1 X 6 inch (2.5 X 15 cm) piece of Hexcel-Schwebel 7544 woven fiberglass mat to the adhesive to form patches having a total thickness of 1.3 mm. The patches were then applied at 70°F (21 °C) to oily steel having dimensions of 1 X 6 X 0.031 inches (2.5 cm X 15 cm X 0.79 mm). A roller was run over the samples twice to provide intimate contact of the adhesive to the metal. The samples were then baked at 182°C for 18 minutes and cooled. The samples were then evaluated in a three-point bend test according to ASTM D790M-93. Results are as reported in Table 2.
- Thermosetting Adhesive 6 was made in the same general way as described in Example 1, except that the rubbers used were Hycar® 2000X162 and Hycar® 1300X8.
- Hycar 2000X162 was a carboxyl-terminated butadiene homopolymer, reported by its manufacturer to have a molecular weight of 4200, an average carboxyl functionality of 1.9 and a glass transition temperature of -77°C.
- the overall proportions of raw materials (exclusive of catalysts) were:
- the acrylonitrile content of Thermosetting Adhesive 6 was 1.6 percent by weight.
Abstract
Description
Claims
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
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BR0111637-1A BR0111637A (en) | 2000-06-06 | 2001-05-30 | Epoxy-based reinforcement patches with improved adhesion to and use of oily metal surfaces |
JP2002502038A JP2004508965A (en) | 2000-06-06 | 2001-05-30 | Epoxy-based reinforced patch with improved adhesion to oily metal surfaces |
DE60107850T DE60107850T2 (en) | 2000-06-06 | 2001-05-30 | ON EPOXY RESIN BASED REINFORCED STRIPS WITH IMPROVED ADHESION ON OILY METAL SURFACES |
AU2001275059A AU2001275059A1 (en) | 2000-06-06 | 2001-05-30 | Epoxy based reinforcing patches with improved adhesion to oily metal surfaces |
CA002411895A CA2411895C (en) | 2000-06-06 | 2001-05-30 | Epoxy based reinforcing patches with improved adhesion to oily metal surfaces |
EP01941730A EP1299497B1 (en) | 2000-06-06 | 2001-05-30 | Epoxy based reinforcing patches with improved adhesion to oily metal surfaces |
MXPA02012118A MXPA02012118A (en) | 2000-06-06 | 2001-05-30 | Epoxy based reinforcing patches with improved adhesion to oily metal surfaces. |
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US20973900P | 2000-06-06 | 2000-06-06 | |
US60/209,739 | 2000-06-06 |
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US (1) | US6586089B2 (en) |
EP (1) | EP1299497B1 (en) |
JP (1) | JP2004508965A (en) |
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CN (1) | CN1229464C (en) |
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CA (1) | CA2411895C (en) |
DE (1) | DE60107850T2 (en) |
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- 2001-05-30 JP JP2002502038A patent/JP2004508965A/en active Pending
- 2001-05-30 KR KR1020027016543A patent/KR100809859B1/en not_active IP Right Cessation
- 2001-05-30 BR BR0111637-1A patent/BR0111637A/en not_active Application Discontinuation
- 2001-05-30 AU AU2001275059A patent/AU2001275059A1/en not_active Abandoned
- 2001-05-30 CA CA002411895A patent/CA2411895C/en not_active Expired - Fee Related
- 2001-05-30 CN CNB018106919A patent/CN1229464C/en not_active Expired - Fee Related
- 2001-05-30 MX MXPA02012118A patent/MXPA02012118A/en active IP Right Grant
- 2001-05-30 WO PCT/US2001/017562 patent/WO2001094493A2/en active IP Right Grant
- 2001-05-30 EP EP01941730A patent/EP1299497B1/en not_active Expired - Lifetime
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WO2006128629A1 (en) | 2005-05-30 | 2006-12-07 | Tesa Ag | Adhesive sheet based on nitrile rubber blends for affixing metal components to plastics |
EP1893709B1 (en) * | 2005-05-30 | 2012-10-10 | Tesa Se | Adhesive sheet based on nitrile rubber blends for affixing metal components to plastics |
WO2006131214A1 (en) * | 2005-06-06 | 2006-12-14 | Tesa Ag | Heat-activated films for fixing metal parts to plastics |
WO2007012656A1 (en) * | 2005-07-28 | 2007-02-01 | Tesa Ag | Adhesive sheet based on nitrile rubber blends for attaching metal parts to plastics |
US7923510B2 (en) | 2005-07-28 | 2011-04-12 | teas SE | Adhesive sheet based on nitrile rubber blends for attaching metal parts to plastics |
US20100028651A1 (en) * | 2008-07-29 | 2010-02-04 | Golden Michael R | Toughened expandable epoxy resins for stiffening and energy dissipation in automotive cavities |
US8153244B2 (en) | 2008-10-15 | 2012-04-10 | 3M Innovative Properties Company | Reinforcement patches with unidirectionally-aligned fibers |
EP2615147A1 (en) * | 2010-09-09 | 2013-07-17 | Kaneka Corporation | Moisture-curable reactive hot-melt adhesive agent composition |
EP2615147A4 (en) * | 2010-09-09 | 2014-01-15 | Kaneka Corp | Moisture-curable reactive hot-melt adhesive agent composition |
CN111315839A (en) * | 2017-08-15 | 2020-06-19 | Ddp特种电子材料美国公司 | Room temperature curable two-part toughened epoxy adhesive |
Also Published As
Publication number | Publication date |
---|---|
CA2411895C (en) | 2009-12-08 |
US20020009582A1 (en) | 2002-01-24 |
CN1433453A (en) | 2003-07-30 |
KR20040030171A (en) | 2004-04-09 |
DE60107850T2 (en) | 2005-12-08 |
US6586089B2 (en) | 2003-07-01 |
KR100809859B1 (en) | 2008-03-04 |
MXPA02012118A (en) | 2004-08-19 |
BR0111637A (en) | 2003-07-01 |
JP2004508965A (en) | 2004-03-25 |
CA2411895A1 (en) | 2001-12-13 |
AU2001275059A1 (en) | 2001-12-17 |
DE60107850D1 (en) | 2005-01-20 |
CN1229464C (en) | 2005-11-30 |
EP1299497B1 (en) | 2004-12-15 |
WO2001094493A3 (en) | 2002-06-20 |
EP1299497A2 (en) | 2003-04-09 |
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