IP Library Granted Patent US 10,947,418
Granted Patent B2
US 10,947,418 · App. 15/972,944 · Granted Mar 16, 2021

Cyanoacrylate compositions

Inventors: Raymond Tully (Slane Meath, IE); Rory Barnes (Dublin, IE); Mark Loane (Dublin, IE); Robert Lambert (Dublin, IE); Cecile Ollagnier (Dublin, IE)
Assignee: Henkel IP & Holding GmbH
C09J4/06C08F222/32C08F222/322
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,947,418
App. No.
15/972,944
Granted
Mar 16, 2021
Kind
B2
Abstract

Cyanoacrylate compositions that include, in addition to an allyl-2-cyanoacrylate, a rubber toughening component and a component functionalized with at least two blocked hydroxyl groups are provided.

Claims (33)

1. A cyanoacrylate composition, comprising:

(a) allyl-2-cyanoacrylate,

(b) a rubber toughening agent comprised of (i) reaction products of the combination of ethylene, methyl acrylate and monomers having carboxylic acid cure sites, (ii) dipolymers of ethylene and methyl acrylate, and combinations of (i) and (ii), and

(c) a component represented by:

wherein A is a C 4 to C 30 aliphatic chain which can optionally comprise heteroatoms selected from the group consisting of O, N and S, and wherein said chain is optionally substituted with one or more acrylate and/or methacrylate functional groups, and/or one or more C 1 -C 10 alkyl groups; and wherein R 1 and R 2 are the same or different and are each optionally selected from the group consisting of H and C 1 to C 6 alkyl.

2. The composition according to claim 1 , further comprising a filler.

3. The composition according to claim 2 , wherein the filler is selected from the group consisting of carbon black, silica and combinations thereof.

4. The composition according to claim 1 , further comprising an acidic stabilizer and a free radical inhibitor.

5. The composition of claim 1 , wherein the rubber toughening agent is present in an amount from 1.5% to 20% by weight.

6. The composition according to claim 1 , further comprising the cyanoacrylate component having the structure H 2 C═C(CN)—COOR, wherein R is selected from the group consisting of C 1-15 alkyl, alkoxyalkyl, cycloalkyl, alkenyl, aralkyl, aryl, and haloalkyl groups.

7. The composition according to claim 6 , wherein the cyanoacrylate component comprises ethyl-2-cyanoacrylate.

8. The composition according to claim 1 , further comprising an accelerator component selected from the group consisting of calixarene, oxacalixarene, silacrown, cyclodextrin, crown ether, poly(ethyleneglycol) di(meth)acrylate, ethoxylated hydric compound, and combinations thereof.

9. The composition according to claim 8 , wherein the calixarene is tetrabutyl tetra[2-ethoxy-2-oxoethoxy]calix-4-arene.

10. The composition according to claim 8 , wherein the crown ether is selected from the group consisting of 15-crown-5, 18-crown-6, dibenzo-18-crown-6, benzo-15-crown-5-dibenzo-24-crown-8, dibenzo-30-crown-10, tribenzo-18-crown-6, asym-dibenzo-22-crown-6, dibenzo-14-crown-4, dicyclohexyl-18-crown-6, dicyclohexyl-24-crown-8, cyclohexyl-12-crown-4, 1,2-decalyl-15-crown-5, 1,2-naphtho-15-crown-5, 3,4,5-naphtyl-16-crown-5, 1,2-methyl-benzo-18-crown-6, 1,2-methylbenzo-5, 6-methylbenzo-18-crown-6, 1,2-t-butyl-18-crown-6, 1,2-vinylbenzo-15-crown-5, 1,2-vinylbenzo-18-crown-6, 1,2-t-butyl-cyclohexyl-18-crown-6, asym-dibenzo-22-crown-6, and 1,2-benzo-1,4-benzo-5-oxygen-20-crown-7 and combinations thereof.

11. The composition according to claim 8 , wherein the poly(ethyleneglycol) di(meth)acrylate is within the following structure:

wherein n is greater than 3.

12. The composition according to claim 1 , further comprising additives selected from the group consisting of shock resistant additives, thixotropy conferring agents, thickeners, dyes, thermal degradation resistance enhancers, and combinations thereof.

13. The composition according to claim 12 , wherein the shock resistant additive is citric acid.

14. The composition according to claim 1 , wherein the component (c) is hexane diol diacrylate.

15. The composition according to claim 1 , further comprising at least one additive selected from the group consisting of: 2-sulfobenzoic acid anhydride, triethylene glycol di(para-toluene sulfonate), trifluoroethyl para-toluene sulfonate, dimethyl dioxolen-4-ylmethyl para-toluene sulfonate, para-toluene sulfonic anhydride, methane sulfonic anhydride, 1,3 propylene sulfite, dioxathiolene dioxide, 1,8-naphthosultone, sultone 1,3-propane, sultone 1,4-butene, allyl phenyl sulfone, 4-fluorophenyl sulfone, dibenzothiophene sulfone, bis(4-fluorophenyl) sulfone, ethyl p-toluenesulfonate, trifluoromethanesulfonic anhydride, ethylene sulphite and tetrafluoroisophthalonitrile and combinations thereof.

16. The composition according to claim 15 , wherein the additive is selected from the group consisting of 1,8-naphthosultone and ethylene sulphite and tetrafluoroisophthalonitrile.

17. The composition according to claim 15 wherein the thermal resistance conferring agent is a mixture of 1,8-naphthosultone and ethylene sulphite.

18. The composition according to claim 1 further comprising a maleimide component.

19. The composition according to claim 18 , wherein the maleimide component has one of the following structures:

R 6 and R 7 are independently selected from C 1 -C 50 alkyl, and C 4 -C 20 aryl, wherein R 6 and R 7 are each independently optionally substituted with one or more of nitro, hydroxyl, halogen, C 1 -C 20 alkyl, C 3 -C 20 cycloalkyl, C 7 -C 20 aralkyl and C 7 -C 20 alkaryl; and R 8 and R 9 are independently selected from H, C 1 -C 50 alkyl, and C 1 -C 50 aryl, or together R 8 and R 9 may form a ring comprising from 5 to 20 carbon atoms.

20. The composition according to claim 19 , wherein the maleimide component is selected from the group consisting of:

21. A method of bonding together two substrates, comprising the steps of:

applying the cyanoacrylate composition according to claim 1 , to at least one of the substrates and

mating together the substrates to permit an adhesive bond to form from the cyanoacrylate composition between the mated substrates.

22. A method of preparing the cyanoacrylate composition according to claim 1 , comprising the steps of:

providing allyl-2-cyanoacrylate component, a rubber toughening agent comprised of (a) reaction products of the combination of ethylene, methyl acrylate and monomers having carboxylic acid cure sites, (b) dipolymers of ethylene and methyl acrylate, and combinations of (a) and (b), and a component represented by:

wherein A is a C 4 to C 30 aliphatic chain which can optionally comprise heteroatoms selected from the group consisting of O, N and S, and wherein said chain is optionally substituted with one or more acrylate and/or methacrylate functional groups, and/or one or more C 1 -C 10 alkyl groups; and wherein R 1 and R 2 are the same or different and are each optionally selected from the group consisting of H and C 1 to C 6 alkyl, and

mixing to form the cyanoacrylate composition.

Assignments (3)
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 Sep 11, 2018
From: TULLY, RAYMOND; BARNES, RORY; LOANE, MARK; LAMBERT, ROBERT; OLLAGNIER, CECILE
To: HENKEL IRELAND OPERATIONS AND RESEARCH LIMITED
Reel/Frame 046838/0366 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 11, 2018
From: HENKEL IRELAND OPERATIONS AND RESEARCH LIMITED
To: HENKEL IP & HOLDING GMBH
Reel/Frame 046838/0457 →