IP Library Granted Patent US 9,574,118
Granted Patent B2
US 9,574,118 · App. 14/266,971 · Granted Feb 21, 2017

Adhesive compositions

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Quick Facts
Patent No.
US 9,574,118
App. No.
14/266,971
Granted
Feb 21, 2017
Kind
B2
Abstract

The present invention provides fast fixturing two part adhesive compositions which include a first part containing a (meth)acrylic component and a cure system for the epoxy resin component of the second part and a second part containing an epoxy resin component and a cure system for the (meth)acrylic component of the first part.

Claims (44)

1. An adhesive composition comprising:

(a) a first part comprising:

(i) a (meth)acrylic component at least a portion of which comprises isobornyl(meth)acrylate in an amount of about 5 to about 35 percent by weight of the total composition;

(ii) an amine catalyst;

(iii) a vinyl terminated polybutadiene in liquid form at room temperature;

(iv) a reactive acid component;

(v) a solid zinc (meth)acrylate salt;

(vi) a zinc and/or bismuth complex; and

(vii) a free-radical inhibitor; and

(b) a second part comprising:

(i) a resin component comprising epoxy groups;

(ii) a benzoyl peroxide; and

(iii) a plasticizer,

wherein when the first and second parts are mixed and applied to at least one substrate, the composition will have up to 5 minutes of open time and when the substrates are mated the composition show a fixture time of less than 90 seconds at a temperature of less than 120° C. at which point the mated assembly can support 3 kg load.

2. The composition of claim 1 , wherein the (meth)acrylic component of part (a) is selected from the group consisting of methyl (meth)acrylate, (meth)acrylic acid, ethyl (meth)acrylate, n-propyl (meth)acrylate, isopropyl (meth)acrylate, n-butyl (meth)acrylate, isobutyl (meth)acrylate, tert-butyl (meth)acrylate, n-pentyl (meth)acrylate, n-hexyl (meth)acrylate, cyclohexyl (meth)acrylate, n-heptyl (meth)acrylate, n-octyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, nonyl (meth)acrylate, decyl (meth)acrylate, dodecyl (meth)acrylate, phenyl (meth)acrylate, tolyl (meth)acrylate, benzyl (meth)acrylate, 2-methoxyethyl (meth)acrylate, 3-methoxybutyl (meth)acrylate, 2-hydroxyethyl (meth)acrylate, 2-hydroxypropyl (meth)acrylate, stearyl (meth)acrylate, glycidyl (meth)acrylate, 2-aminoethyl (meth)acrylate, γ-(meth)acryloyloxypropyl trimethoxysilane, (meth)acrylic acid-ethylene oxide adduct, trifluoromethylmethyl (meth)acrylate, 2-trifluoromethylethyl (meth)acrylate, 2-perfluoroethylethyl (meth)acrylate, 2-perfluoroethyl-2-perfluorobutylethyl (meth)acrylate, 2-perfluoroethyl (meth)acrylate, perfluoromethyl (meth)acrylate, diperfluoromethylmethyl (meth)acrylate, 2-perfluoromethyl-2-perfluoroethylmethyl (meth)acrylate, 2-perfluorohexylethyl (meth)acrylate, 2-perfluorodecylethyl (meth)acrylate, 2-perfluorohexadecylethyl (meth)acrylate, ethoxylated trimethylolpropane triacrylate, trimethylol propane trimethacrylate, dipentaerythritol monohydroxypentacrylate, pentaerythritol triacrylate, ethoxylated trimethylolpropane triacrylate, 1,6-hexanedioldiacrylate, neopentyl glycoldiacrylate, pentaerythritol tetraacrylate, 1,2-butylene glycoldiacrylate, trimethylopropane ethoxylate tri(meth)acrylate, glyceryl propoxylate tri(meth)acrylate, trimethylolpropane tri(meth)acrylate, dipentaerythritol monohydroxy penta(meth)acrylate, tri(propylene glycol) di(meth)acrylate, neopentylglycol propoxylate di(meth)acrylate, 1,4-butanediol di(meth)acrylate, polyethyleneglycol di(meth)acrylate, triethyleneglycol di(meth)acrylate, butylene glycol di(meth)acrylate, ethoxylated bisphenol A di(meth)acrylate, and combinations thereof.

3. The composition of claim 1 , wherein the amine is selected from the group consisting of 1,8-diazabicyclo(5.4.0)undec-7-ene, 1,4-diazabicyclo(2.2.2)octane, triethylamine, tetramethylguanidine, dimethyl-p-toluidine, dimethyl aniline, dihydroxyethyl aniline, dihydroxy ethyl p-toluidine, dimethyl-o-toluidine, dimethyl aniline, and benzoyl-thiourea, a trialkyl amine, tributyl amine, dihydro pyridine, phenyl dihydro pyridine, dihydropyridine derivatives, aldehyde condensation products of alkyl, aromatic, heterocyclic amines, and combinations thereof.

4. The composition of claim 1 , wherein the reactive acid component is sulphonic acid or sulphonic acid derivatives.

5. The composition of claim 1 , wherein the reactive acid component is selected from the group consisting of phosphoric acid, phosphoric acid derivatives, and phosphate esters.

6. The composition of claim 1 , wherein the reactive acid component is a phosphate ester comprising a compound of the formula:

wherein R 1 is H or CH 3 , and R 2 is H or:

7. The composition of claim 1 , wherein the reactive acid component is hydroxyl ethyl methacrylate phosphate ester.

8. The composition of claim 1 , wherein the free radical inhibitor is selected from the group consisting of quinones, hydroquinones, hydroxylamines, nitroxyls, phenols, amines, amines, quinolines, phenothiazines, and combinations thereof.

9. The composition of claim 1 , wherein the free radical inhibitor is selected from the group consisting of hydroquinone, tertiary butylhydroquinone, phenothiazine, methyl hydroquinone, hydroxyethylhydroquinone, N-alkyl substituted p-phenylenediamines, and combinations thereof.

10. The composition of claim 1 , wherein the epoxy resin of part (b) is selected from the group consisting of cycloaliphatic epoxides, epoxy novolac resins, bisphenol-A epoxy resins, bisphenol-F epoxy resins, bisphenol-A epichlorohydrin based epoxy resin, alkyl epoxides, limonene dioxide, polyfunctional epoxides, and combinations thereof.

11. The composition of claim 1 , wherein the epoxy resin of part (b) is a liquid bisphenol A epichlorohydrin epoxy resin.

12. A method of preparing a two-part adhesive composition of claim 1 , comprising the steps of:

(a) providing a first part of the adhesive composition comprising:

(i) a (meth)acrylic component at least a portion of which comprises isobornyl(meth)acrylate;

(ii) an amine catalyst;

(iii) a vinyl terminated polybutadiene in liquid form at room temperature;

(iv) a reactive acid component;

(v) a solid zinc (meth)acrylate salt;

(vi) a zinc and/or bismuth complex; and

(vii) a free-radical inhibitor; and

(b) providing a second part of the adhesive composition comprising:

(i) a resin component comprising epoxy groups;

(ii) a benzoyl peroxide;

(iii) a plasticizer; and

(vi) optionally, a block copolymer.

13. A method of bonding a first surface to a second surface, comprising:

providing a two part adhesive composition of claim 1 , providing a first surface to be bonded and a second surface to be bonded, dispensing with mixing the two part adhesive composition onto at least one of the first surface or the second surface, mating the first surface and the second surface with the adhesive composition between the mated first surface of the second surface, and forming an adhesive bond therebetween.

14. The method of claim 12 , wherein the first part and second are mixed in a ratio of 0.5 to 15 parts part (a) to one part (b) by volume.

15. The composition of claim 1 , wherein the (meth)acrylic component of part (a) further comprises methyl (meth)acrylate.

16. The composition of claim 1 , wherein part (a) further comprises a block copolymer.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 9, 2022
From: HENKEL IP & HOLDING GMBH
To: HENKEL AG & CO. KGAA
Reel/Frame 059357/0267 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 27, 2015
From: HENKEL CORPORATION
To: HENKEL US IP LLC
Reel/Frame 035049/0904 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 27, 2015
From: HENKEL US IP LLC
To: HENKEL IP & HOLDING GMBH
Reel/Frame 035050/0378 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 1, 2014
From: CHENG, CHIH-MIN; MURRAY, JAMES; SCHUFT, CHARLES
To: HENKEL CORPORATION
Reel/Frame 032798/0891 →