US4612209A
Expired / Lapsed
US
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Process for the preparation of heat-curable adhesive films
Assignee: Novartis Corp
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Filing: 1984-12-17
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Granted: 1986-09-16
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Expires: 2004-12-17
Abstract
Abstract Heat-curable adhesive films of variable tack can be prepared: 1. by coating a peelable release film or substrate with a liquid mixture of substances containing (a) 2-24% by weight of a photopolymerizable compound containing at least one grouping CH 2 ═C(R)COO-- in which R is a hydrogen atom or a methyl group, (b) 20-90% by weight of a heat-curable epoxide resin or mixture of epoxide resins containing no photopolymerizable groups, (c) a heat-activatable curing agent for epoxide resins, (d) 0.1 to 2% by weight of an accelerator, (e) 0.01 to 5% by weight of a photopolymerization catalyst for the component (a) and (f) if appropriate, further additives, the sum of the components (a) to (f) being 100% by weight, 2. by covering the layer, if necessary, with a reinforcing material and again coating with a mixture of substances according to 1, and 3. irradiating the layer thus obtained with actinic light.
Inventors
- 👤 Imre Forgo
- 👤 Rene Huwyler
- 👤 Jacques Francois
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-27 08:34
CPC Classifications
C; C09; C09J; C09J4/00; C09J4/06; C08; C08F; C08F283/00; C08F283/10; C09J7/00; C09J7/10
Claims Analysis
Total Claims: 15
Claim 1
Independent Claim
150 words
A process for the preparation of heat-curable adhesive films of variable tack, which consist essentially of coating a peelable release film or substrate with a liquid mixture of substances containing (a) 2-24% by weight of a photopolymerisable compound containing at least one grouping CH 2 ═C(R)COO-- in which R is a hydrogen atom or a methyl group, (b) 20-90% by weight of a heat-curable epoxide resin or mixture of epoxide resins containing no photopolymerisable groups, (c) a heat-activatable curing agent for epoxide resins, (d) 0.1 to 2% by weight of an accelerator, (e) 0.01 to 5% by weight of a photopolymerisation catalyst for the component (a), the sum of the components (a) to (e) being 100% by weight, covering the layer, if appropriate, with a reinforcing material and coating it again with a mixture of substances according to the first step, and irradiating the layer thus obtained with actinic light.
Claim 2
Dependent Claim
150 words
A process for the preparation of heat-curable adhesive films of variable tack, which consist essentially of coating a peelable release film or substrate with a liquid mixture of substances containing (a) 2-24% by weight of a photopolymerisable compound containing at least one grouping CH 2 ═C(R)COO-- in which R is a hydrogen atom or a methyl group, (b) 20-90% by weight of a heat-curable epoxide resin or mixture of epoxide resins containing no photopolymerisable groups, (c) a heat-activatable curing agent for epoxide resins, (d) 0.1 to 2% by weight of an accelerator, (e) 0.01 to 5% by weight of a photopolymerisation catalyst for the component (a), the sum of the components (a) to (e) being 100% by weight, covering the layer, if appropriate, with a reinforcing material and coating it again with a mixture of substances according to the first step, and irradiating the layer thus obtained with actinic light.
Claim 3
Dependent Claim
114 words
A process according to claim 1, wherein compounds of the formula I ##STR11## in which R is a hydrogen atom or a methyl group, n is an integer from 1 to 4 and, if n=1, X is alkyl having 1-12 C atoms, hydroxyalkyl having 1-4 C atoms, alkoxyalkyl having 2-8 C atoms, ##STR12## cyclopentyl, cyclohexyl, phenyl, 2-furyl, 2-pyridyl or 3-pyridyl, or, if n=2, X is a group --C r H 2r -- in which r=2-12, --[CH 2 CH 2 O] m CH 2 CH 2 -- in which m=1, 2 or 3 or ##STR13## if n=3, X is ##STR14## and, if n =4, X is a group ##STR15## are used as the component (a).
Claim 4
Dependent Claim
96 words
A process as claimed in claim 2, wherein a compound of the formula I in which R is a hydrogen atom or a methyl group, n is an integer from 1 to 4 and, if n=1, X is hydroxyalkyl having 2 or 3 C atoms or alkoxyalkyl having 2-6 C atoms, if n=2 X is a group --(CH 2 ) r -- in which r=2-6 or --CH 2 CH 2 OCH 2 CH 2 -- or ##STR16## if n=3 X is ##STR17## and, if n=4, X is ##STR18## or mixtures of the said compounds are used.
Claim 5
Dependent Claim
60 words
A process according to claim 1, wherein ethylene glycol dimethacrylate, 1,4-butanediol diacrylate or 1,4-butanediol dimethacrylate, 1,6-hexanediol diacrylate or 1,6-hexanediol dimethacrylate, 2-hydroxyethyl diacrylate, 2-hydroxyethyl dimethacrylate, 2-hydroxypropyl diacrylate, 2-hydroxypropyl dimethacrylate, 3-hydroxypropyl diacrylate or 3-hydroxypropyl dimethacrylate, 2-methoxyethyl acrylate, 2-methoxyethyl dimethacrylate, 2-ethoxyethyl acrylate or 2-ethoxyethyl dimethacrylate, 1,1,1-trimethylolpropane triacrylate or 1,1,1-trimethylolpropane trimethacrylate, pentaerythritol triacrylate or pentaerythritol trimethacrylate or mixtures thereof are used as component (a).
Claim 6
Dependent Claim
84 words
A process according to claim 1, wherein an epoxide resin having on average more than one group of the formula II ##STR19## attached to an S, O or N atom, in which Q and Q 2 are each a hydrogen atom and Q 1 is a hydrogen atom or a methyl group, or Q and Q 2 together are --CH 2 CH 2 -- or --CH 2 --CH 2 CH 2 -- and Q 1 is a hydrogen atom is used as component (b).
Claim 7
Dependent Claim
36 words
A process according to claim 1, wherein a diglycidyl ether, which can be so-called advanced, of 2,2-bis-(4-hydroxyphenyl)-propane, 2,2-bis-(3,5-dibromo-4-hydroxyphenyl)-propane, bis-(4-hydroxyphenyl)-methane, bis-(4-hydroxycyclohexyl)-methane or 2,2-bis-(4-hydroxycyclohexyl)-propane, a polyglycidyl ether of a novolak or tetraglycidylated 4,4'-diaminodiphenylmethane is used as component (b).
Claim 8
Dependent Claim
39 words
A process according to claim 1, wherein a diglycidyl ether, which can be so-called advanced, of bisphenol A, tetrabromobisphenol A or bisphenol F, a polyglycidyl ether of phenol-formaldehyde or cresol-formaldehyde novolaks or mixtures thereof are used as component (b).
Claim 9
Dependent Claim
15 words
A process according to claim 1, wherein dicyandiamide is used as the curing agent (c).
Claim 10
Dependent Claim
72 words
A process according to claim 1, wherein a compound of the formula III ##STR20## in which R 1 and R 2 independently of one another are alkyl having 1-4 C atoms, R 3 and R 4 independently of one another are a hydrogen or halogen atom, alkyl or alkoxy having 1-4 C atoms, phenyl or phenoxy and R 5 is a hydrogen atom or --CF 3 is used as the accelerator (d).
Claim 11
Dependent Claim
14 words
A process according to claim 1, wherein chlortoluron is used as the accelerator (d).
Claim 12
Dependent Claim
17 words
A process according to claim 1, wherein benzil dimethyl ketal is used as the photopolymerisation catalyst (e).
Claim 13
Dependent Claim
31 words
A process according to claim 1, wherein inorganic fillers, surface-active substances or elastomers are used as further additives (f), the sum of the components (a) to (f) being 100% by weight.
Claim 14
Dependent Claim
39 words
A process according to claim 1, wherein a mixture of substances containing 4-20% by weight of component (a), 30-90% by weight of component (b), 0.1-1.0% by weight of component (d) and 0.02-1.0% by weight of component (e) is used.
Claim 15
Dependent Claim
64 words
A process according to claim 1, wherein the resulting adhesive films are coated with a heat-curable epoxide resin system containing (i) an epoxide resin or mixture of epoxide resins which is dispersed, in a finely divided form, in (ii) a thermoplastic copolymer formed from an α-olefin and an ether or ester of an α-olefin, and (iii) a curing agent for the epoxide resin (i).
References Cited (Backward Citations)
US3641195A
Cited
US4092443A
Cited
GB1552046A
Cited
GB2105726A
Cited
GB2109798A
Cited
US4440802A
Cited
GB2119810A
Cited
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| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
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| 3.5 Years (Year 4) | 1989-09-15 | 1990-03-17 | 1990-09-16 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1993-09-15 | 1994-03-17 | 1994-09-16 | $3760.00 | Window Closed / Lapsed |
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