IPC분류정보
국가/구분 |
United States(US) Patent
등록
|
국제특허분류(IPC7판) |
|
출원번호 |
US-0868566
(1999-12-10)
|
우선권정보 |
DE-0058921 (1998-12-19) |
국제출원번호 |
PCT/EP99/09732
(1999-12-10)
|
국제공개번호 |
WO00/37554
(2000-06-29)
|
발명자
/ 주소 |
|
출원인 / 주소 |
|
대리인 / 주소 |
|
인용정보 |
피인용 횟수 :
43 인용 특허 :
8 |
초록
▼
A high strength adhesive having a good impact strength at low temperatures, below 0° C., and at temperatures of 90° C. is provided. The adhesive comprises a copolymer having at least one glass transition temperature of −30° C. or lower having epoxy reactive end groups or a reac
A high strength adhesive having a good impact strength at low temperatures, below 0° C., and at temperatures of 90° C. is provided. The adhesive comprises a copolymer having at least one glass transition temperature of −30° C. or lower having epoxy reactive end groups or a reaction product of the copolymer with a polyepoxide, a reaction product of a polyurethane prepolymer and a polyphenol or polyaminophenol and at least one epoxy resin.
대표청구항
▼
1. A structural adhesive composition with good low temperature impact strength which comprises:A) A copolymer having at least one glass transition temperature of −30° C. or lower and epoxy-reactive groups or a reaction product of this copolymer with a polyepoxide;B) A reaction product of
1. A structural adhesive composition with good low temperature impact strength which comprises:A) A copolymer having at least one glass transition temperature of −30° C. or lower and epoxy-reactive groups or a reaction product of this copolymer with a polyepoxide;B) A reaction product of a polyurethane prepolymer with a polyphenol or aminophenol;C) At least one epoxy resin;D) A hardener and optionally a hardening accelerator;E) Optionally at least one member selected from the group consisting of plasticizers, reactive diluents, rheology aids, fillers, wetting agents, antiagers and stabilizers;F) At least one polyester polyol with a molecular weight of 400 to 5,000; andG) Optionally a thermoplastic polymer powder. 2. The composition claimed in claim 1, wherein component A) comprises a butadiene-based copolymer. 3. The composition claimed in claim 2, wherein the copolymer of component A) comprises a carboxyl-containing copolymer based on at least one member selected from the group consisting of butadiene/acrylonitrile copolymer, butadiene/(meth)acrylate copolymer, butadiene/acrylonitrile/styrene copolymer and butadiene/(meth)acrylate/styrene copolymer. 4. The composition claimed in claim 1, wherein the copolymer of component A) comprises a core/shell polymer of which the core polymer is a diene polymer or a (meth)acrylate polymer with a glass transition temperature of −30° C. or lower and which may optionally be crosslinked with 0.01 to 5% by weight of a diolefinic comonomer and of which the shell polymer has a glass transition temperature of 60° C. or higher and contains residues of at least one monomer selected from the group consisting of alkyl (meth)acrylate, (meth)acrylonitrile, (methyl) styrene, olefinically unsaturated carboxylic acids, olefinically unsaturated carboxylic anhydrides and mixtures thereof. 5. The composition claimed in claim 1 wherein component A comprises an adduct of an epoxy resin and a butadiene based copolymer. 6. The composition claimed in claim 1 wherein component B) comprises a compound of the formula: 1 —[X—(C═O)—NH—R 2 —NH—(C═O)—Y—R 2 —(X) m ] n (I)in whichm=1 or 2,n=2 or 3,R 1 is a residue of a polyalkylene glycol after removal of the functional groups (hydroxyl or amino groups),R 2 is C 6-18 alkyl, aryl, aralkyl (residue of a diisocyanate after removal of the isocyanate groups), X, Y is —O—, —S— or —NR 4 —, where R 4 ═H or C 1-4 alkyl or phenyl,R 3 is a carbocyclic-aromatic or araliphatic m+1-functional residue with groups Z directly attached to an aromatic ring and Z is —OH or —NHR 4 (residue of a polyphenol or aminophenol after removal of the functional groups). 7. The composition claimed in claim 1, wherein component B) is dissolved in a liquid polyepoxide. 8. The composition claimed in claim 1, wherein component B) is reacted with a stoichiometric excess of a polyepoxide. 9. The composition claimed in claim 1 whereinD) comprises a latent hardener selected from the group consisting of dicyanodiamide, guanamines, guanidines, aminoguanidines, solid aromatic diamines and mixtures thereof and optionally a hardening accelerator. 10. A cured composition of claim 1 having an impact peel energy of at least 5 J at −20° C. (to ISO 11343). 11. The production of composite materials, potting compounds in the electrical and electronics industries and die-attach adhesive for the production of circuit boards in the electronics industry wherein the adhesive comprises the composition of claim 10. 12. The method for hardening a composition of claim 1 which comprises heating the composition to a temperature of 80° C. to 210° C. 13. A method for bonding substrates selected from the group consisting of metallic materials composite materials and combinations thereof comprising:1) applying an adhesi ve composition comprising:A) 5% to 25% by weight of the adhesive composition of a copolymer with at least one glass transition temperature of −30° C. or lower and groups reactive with epoxy resins or a reaction product of the copolymer with a polyepoxide in stoichiometric excess;B) 5% to 30% by weight of adhesive composition of a product of the reaction of a polyurethane prepolymer with a polyphenol or an aminophenol;C) 10% to 60% by weight of the adhesive composition of an epoxy resin, wherein the epoxy resin comprises a mixture of liquid and optionally solid epoxy resins and optionally low molecular weight epoxy resins as reactive diluents;D) 1% to 10% by weight of the adhesive composition of a hardener, to one of the surfaces of a substrate to be joined, optionally after at least one of cleaning and surface treatment;2) fitting the substrates to be joined together;3) optionally pregelling the adhesive composition; and4) curing the adhesive composition by heating the substrates to a temperature of from 80° C. to 210° C.; whereby, a joint with a lap shear strength at room temperature of at least 15 Mpa and a lap shear strength at 90° C. greater than 10 Mpa, when the substrates are steel, is formed, and wherein a low temperature impact resistance measured according to ISO 11343 at −20° C. as impact peel energy is at least 5J at 2 m/sec. and wherein B) comprises residues of at least one of hydroxy or amino terminated polytetramethylene glycols. 14. The method of claim 15 wherein the adhesive composition is cured at a temperature of from 120° C. to 180° C. 15. The method of claim 12 wherein the composition is heated at a temperature of from 120° C. to 180° C. 16. The method of claim 13 wherein the adhesive composition further comprises:D) a latent hardener selected from the group consisting of dicyanodiamide, guanamines, guanidines, aminoguanidines, solid aromatic diamines and mixtures thereof and optionally a hardening accelerator;E) optionally at least one further member selected from the group consisting of plasticizers, reactive diluents, rheological auxiliaries, fillers, wetting agents, antiagers and mixtures thereof;F) a polyesterpolyol with a molecular weight of from 400 to 5,000; andG) optionally a thermoplastic polymer powder. 17. The method of claim 13 wherein B) comprises a compound of the formula: 1 —[X—(C═O)—NH—R 2 —NH—(C═O)—Y—R 3 —(X) m ] n . 18. The structural adhesive composition of claim 1; wherein,A) comprises from 5% to 25% by weight of the composition;B) comprises 5% to 30% by weight of the composition;C) comprises 10% to 60% by weight of composition; andD) comprises 1% to 10% by weight of the composition.
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