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US4525232A Expired / Lapsed US ⏱️ 0.0 years remaining

Polymerizable acrylic compositions having vinyl ether additive

Assignee: Henkel Loctite Ireland Ltd
•
Filing: 1984-04-16
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Granted: 1985-06-25
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Expires: 2004-04-16
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Abstract

Abstract Polymerization of acid activated compositions of acrylic monomers, peroxy initiators and ferrocene derivatives is inhibited by addition of 0.5-20% of a vinyl ether monomer. Bulk compositions activated by addition of a strong acid can be provided with a desired polymerization induction time directly related to the concentration of the vinyl ether. Compositions containing compounds which decompose to a strong acid upon exposure to actinic radiation, thereby activating polymerization, have increased shelf lives when vinyl ethers are included therein. The use of vinyl ether monomers having a functionality of two or more also provides increased adhesive bond strength after curing.

Inventors

  • 👤 John M. Rooney
  • 👤 John Woods
  • 👤 Paul Conway

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-25 12:44
CPC Classifications
C; C09; C09J; C09J4/00

Claims Analysis

Total Claims: 18
Claim 1
Independent Claim 64 words
In a curable composition activatable by a strong acid comprising an acrylic monomer selected from the group comprising di- and poly-(meth)acrylate esters and monofunctional (meth)acrylate esters having a polar group selected from labile hydrogen, heterocyclic ring, hydroxy, amino, cyano, and halogen groups; a peroxy initiator; and a ferrocene compound, the improvement comprising that the composition further comprises from 0.5-20% of a vinyl ether monomer.
Claim 2
Dependent Claim 64 words
In a curable composition activatable by a strong acid comprising an acrylic monomer selected from the group comprising di- and poly-(meth)acrylate esters and monofunctional (meth)acrylate esters having a polar group selected from labile hydrogen, heterocyclic ring, hydroxy, amino, cyano, and halogen groups; a peroxy initiator; and a ferrocene compound, the improvement comprising that the composition further comprises from 0.5-20% of a vinyl ether monomer.
Claim 3
Dependent Claim 12 words
An activated composition as in claim 1 further comprising said strong acid.
Claim 4
Dependent Claim 7 words
A cured composition as in claim 2.
Claim 5
Dependent Claim 31 words
A composition as in claim 2, wherein said strong acid is selected from saccharin, perchloric acid, sulfonic acids, phosphonic acids, maleic acid, acetylene carboxylic acid, acetylene dicarboxylic acid or malonic acid.
Claim 6
Dependent Claim 22 words
A composition as in claim 1 further comprising a compound which decomposes upon exposure to actinic radiation to release a strong acid.
Claim 7
Dependent Claim 86 words
A composition as in claim 5 wherein the radiation decomposible compound is a salt of a complex halogenide having the formula [A] d + [MX e ] - (e-f) where A is a cation selected from the group consisting of iodonium, sulfonium, thiopyrylium and diazonium cations, M is a metalloid, X is a halogen radical, d=e-f, f=the valence of M and is an integer equal to from 2 to 7 inclusive, e is greater than f and is an integer having a value up to 8.
Claim 8
Dependent Claim 13 words
The composition of claim 1 wherein the peroxy initiator is an organic hydroperoxide.
Claim 9
Dependent Claim 23 words
The composition of claim 7 wherein the organic hydroperoxide is present at levels of between 0.1 and 10% by weight of the composition.
Claim 10
Dependent Claim 19 words
The composition of claim 7 wherein the organic hydroperoxide is selected from cumene hydroperoxide, t-butyl hydroperoxide and methylethylketone hydroperoxide.
Claim 11
Dependent Claim 28 words
The composition of claim 1 wherein the ferrocene compound is selected from ferrocene, t-octyl ferrocene, acetyl ferrocene, benzoyl ferrocene, hydroxyethyl ferrocene, 1,1'-dibutyl ferrocene, n-butyl ferrocene and ferrocene polymers.
Claim 12
Dependent Claim 121 words
The composition of claim 1 wherein the vinyl ether monomer is represented by one of the following formulas: (CH 2 ═CH--O--CH 2 ) n --G; (CH 2 ═CH--O--C 6 H 4 ) n --G; (CH 2 ═CH--O--CR 1 ═CR 2 ) n --G; or (CH 2 ═CH--O--C.tbd.C) n --G, or ketene acetals such as those of the formula: ##STR2## where n is an integer greater than or equal to one; G is a mono or multivalent radical free of groups which intefere with cationic or free radical polymerization; R 1 and R 2 are selected from H, hydrocarbonyl or substituted hydrocarbonyl; R 3 is hydrocarbonyl or substituted hydrocarbonyl; and Y is a hydrocarbonyl group having between 1 and 5 carbon atoms.
Claim 13
Dependent Claim 11 words
The composition of claim 11 wherein n is greater than 1.
Claim 14
Dependent Claim 25 words
The composition of claim 11 wherein the vinyl ether is selected from n-butyl vinyl ether, 1,4-butanediol divinyl ether, 2-chloroethyl vinyl ether and ethyl vinyl ether.
Claim 15
Dependent Claim 40 words
A process of sealing or bonding substrates which comprises applying to at least one of said substrates an activated composition as in Claim 2, and joining said substrates until said composition has cured sufficiently to bond or seal said substrates.
Claim 16
Dependent Claim 55 words
The process of claim 14 wherein said applying step comprises: (a) applying a composition comprising said acrylic monomer, peroxy initiator, ferrocene compound, and vinyl ether monomer ingredients, and a compound which decomposes upon exposure to actinic radiation to release a strong acid, to said substrate; and (b) irradiating said composition to release the strong acid.
Claim 17
Dependent Claim 53 words
A method as in claim 14 wherein the applying step comprises applying to at least one of said substrates a primer comprising at least one of said strong acid or said ferrocene ingredients and subsequently applying to at least one of said substrates a composition comprising the remaining ingredients of said activated composition.
Claim 18
Dependent Claim 18 words
A method as in claim 14 wherein said composition is activated in bulk prior to said applying step.

References Cited (Backward Citations)

US3424638A Cited
US3702812A Cited
US3855040A Cited
JPS5156891A Cited
US4245029A Cited
DE3010373A1 Cited
US4451615A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1988-06-24 1988-12-24 1989-06-25 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1992-06-24 1992-12-24 1993-06-25 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1996-06-24 1996-12-24 1997-06-25 $7700.00 Window Closed / Lapsed

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