Patent US4056670A successfully refreshed from Google Patents.
← Back to Patent Explorer
US4056670A Expired / Lapsed US ⏱️ 0.0 years remaining

Anaerobic adhesive and sealant compositions employing as a catalyst α-

Assignee: Ingredion Inc
•
Filing: 1975-11-03
•
Granted: 1977-11-01
•
Expires: 1995-11-03
📄 Original PDF 🌐 Google Patents 🔄 Sync Now

Abstract

Abstract Anaerobic curing compositions useful as anaerobic adhesives and sealants are described. These compositions comprise mixtures of polymerizable acrylic and substituted acrylic monomers together with a catalyst comprising an alpha-amino sulfone compound.

Inventors

  • 👤 Martin M. Skoultchi

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-02 18:23
CPC Classifications
C; C08; C08F; C08F222/00; C08F222/10; C08F222/1006; C08F222/102; C09; C09J; C09J4/00

Claims Analysis

Total Claims: 10
Claim 1
Independent Claim 485 words
An anaerobic curing composition stable when exposed to air consisting essentially of a mixture of a polymerizable acrylic or substituted acrylic monomer selected from the group consisting of ##STR14## wherein R is selected from the group consisting of hydrogen, methyl, ethyl, ##STR15## R' is selected from the group consisting of hydrogen chlorine, methyl and ethyl; R" is selected from the group consisting of hydrogen, hydroxy, ##STR16## m is an integer from 1 to 8; and n is an integer from 1 to 20; and p is 0 or 1; ##STR17## wherein R represents hydrogen, chlorine, methyl or ethyl, R' represents alkylene with 2-6 carbon atoms, R" represents (CH 2 ) m in which m is an integer of from 0 to 8, ##STR18## n represents an integer of from 1 to 4; ##STR19## wherein X is selected from the group consisting of --0-- and ##STR20## and R is a member selected from the group consisting of hydrogen and lower alkyl of 1 to 7 carbon atoms, A represents the organic residue of an active hydrogen containing acrylic ester wherein the active hydrogen has been removed, said ester being hydroxy or amino substituted on the alkyl protion thereof, and the methyl, ethyl and chlorine homologs thereof, n is an integer from 1 to 6, and B is a mono- or polyvalent organic radical selected from the group consisting of alkyl, alkylene, alkenyl, cycloalkyl, cycloalkylene, aryl, aralkyl, alkaryl, poly(oxyalkylene) poly(carboalkoxyalkylene), and heterocyclic radicals both substituted and unsubstituted ##STR21## wherein R 1 is selected from the group consisting of methyl, ethyl, carboxyl and hydrogen, R 2 is selected from the group consisting of hydrogen, methyl and ethyl; R 3 is selected from the group consisting of hydrogen, methyl and hydroxyl; R 4 is selected from the group consisting of hydrogen, chlorine, methyl and ethyl and n represents an integer of from 0 to 8; and e. monofunctional acrylate and methacrylate esters and the hydroxy, amide, cyano, chloro, and silane substituted derivatives thereof; and from 0.05 to 5.0%, by weight of monomer, of an alpha-amino sulfone corresponding to the formula ##STR22## where R is hydrogen or methyl; R 1 , R 2 and R 3 are independently chosen from the group consisting of hydrogen; hydroxy; C 1 -C 20 alkyl; C 1 -C 20 alkyl substituted with chlorine, bromine, fluorine, dialkyl(C 1 -C 6 )amino, carboalkoxy (C 1 -C 4 ) or alkoxy (C 1 -C 4 ); C 6 -C 10 aryl; C 6 -C 10 aryl substituted with alkyl (C 1 -C 8 ), chlorine, bromine, fluorine, dialkyl(C 1 -C 6 )amino, carboalkoxy (C 1 -C 4 ) or alkoxy (C 1 -C 4 ); dialkyl(C 1 -C 6 )amino, or either R 2 or R 3 may be ##STR23## and wherein the alpha-amino sulfone is present in amount sufficient to initiate polymerization of said acrylic monomer at room temperature in the absence of air or oxygen.
Claim 2
Dependent Claim 485 words
An anaerobic curing composition stable when exposed to air consisting essentially of a mixture of a polymerizable acrylic or substituted acrylic monomer selected from the group consisting of ##STR14## wherein R is selected from the group consisting of hydrogen, methyl, ethyl, ##STR15## R' is selected from the group consisting of hydrogen chlorine, methyl and ethyl; R" is selected from the group consisting of hydrogen, hydroxy, ##STR16## m is an integer from 1 to 8; and n is an integer from 1 to 20; and p is 0 or 1; ##STR17## wherein R represents hydrogen, chlorine, methyl or ethyl, R' represents alkylene with 2-6 carbon atoms, R" represents (CH 2 ) m in which m is an integer of from 0 to 8, ##STR18## n represents an integer of from 1 to 4; ##STR19## wherein X is selected from the group consisting of --0-- and ##STR20## and R is a member selected from the group consisting of hydrogen and lower alkyl of 1 to 7 carbon atoms, A represents the organic residue of an active hydrogen containing acrylic ester wherein the active hydrogen has been removed, said ester being hydroxy or amino substituted on the alkyl protion thereof, and the methyl, ethyl and chlorine homologs thereof, n is an integer from 1 to 6, and B is a mono- or polyvalent organic radical selected from the group consisting of alkyl, alkylene, alkenyl, cycloalkyl, cycloalkylene, aryl, aralkyl, alkaryl, poly(oxyalkylene) poly(carboalkoxyalkylene), and heterocyclic radicals both substituted and unsubstituted ##STR21## wherein R 1 is selected from the group consisting of methyl, ethyl, carboxyl and hydrogen, R 2 is selected from the group consisting of hydrogen, methyl and ethyl; R 3 is selected from the group consisting of hydrogen, methyl and hydroxyl; R 4 is selected from the group consisting of hydrogen, chlorine, methyl and ethyl and n represents an integer of from 0 to 8; and e. monofunctional acrylate and methacrylate esters and the hydroxy, amide, cyano, chloro, and silane substituted derivatives thereof; and from 0.05 to 5.0%, by weight of monomer, of an alpha-amino sulfone corresponding to the formula ##STR22## where R is hydrogen or methyl; R 1 , R 2 and R 3 are independently chosen from the group consisting of hydrogen; hydroxy; C 1 -C 20 alkyl; C 1 -C 20 alkyl substituted with chlorine, bromine, fluorine, dialkyl(C 1 -C 6 )amino, carboalkoxy (C 1 -C 4 ) or alkoxy (C 1 -C 4 ); C 6 -C 10 aryl; C 6 -C 10 aryl substituted with alkyl (C 1 -C 8 ), chlorine, bromine, fluorine, dialkyl(C 1 -C 6 )amino, carboalkoxy (C 1 -C 4 ) or alkoxy (C 1 -C 4 ); dialkyl(C 1 -C 6 )amino, or either R 2 or R 3 may be ##STR23## and wherein the alpha-amino sulfone is present in amount sufficient to initiate polymerization of said acrylic monomer at room temperature in the absence of air or oxygen.
Claim 3
Dependent Claim 15 words
The composition of claim 1 wherein the alpha-amino sulfone is N-(p-carboethoxyphenyl)-(p-tolylsulfonemethyl) amine or N-(o-carboethoxyphenyl)-(p-tolylsulfonemethyl) amine.
Claim 4
Dependent Claim 12 words
The composition of claim 1 wherein the monomer is polymerizable hydroxyethyl methacrylate.
Claim 5
Dependent Claim 12 words
The composition of claim 1 wherein the monomer is polymerizable hydroxypropyl methacrylate.
Claim 6
Dependent Claim 30 words
The composition of claim 1 wherein the monomer is the polymerizable reaction product of 2 moles of toluene diisocyanate, 1 mole of poly(propylene glycol) and 2 moles of hydroxyethyl acrylate.
Claim 7
Dependent Claim 23 words
The composition of claim 1 where there is additionally present in the composition 0.05 to 5.0% by weight of the monomer of ortho-sulfobenzimide.
Claim 8
Dependent Claim 27 words
The composition of claim 1 where there is additionally present in the composition from 0.1 to 10% by weight of the total composition of a dialkyl peroxide.
Claim 9
Dependent Claim 13 words
The composition of claim 7 wherein the dialkyl peroxide is dicumylperoxide or di-t-butylpeoxide.
Claim 10
Dependent Claim 23 words
The composition of claim 7 where there is additionally present in the composition 0.05 to 5.0% by weight of the monomer of ortho-sulfobenzimide.

References Cited (Backward Citations)

US2750357A Cited
US3435012A Cited
US3625930A Cited
US3616040A Cited
US3775385A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1980-10-31 1981-05-02 1981-11-01 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1984-10-31 1985-05-02 1985-11-01 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1988-10-31 1989-05-02 1989-11-01 $7700.00 Window Closed / Lapsed

Assigned Categories & Tags

No categories assigned to this patent yet.

Assign Category Tag