IP Library Granted Patent US 8,916,622
Granted Patent B2
US 8,916,622 · App. 13/515,365 · Granted Dec 23, 2014

Heat-curable epoxy functional composition and transparent heat-cured caustic-resistant hard-coatings prepared therefrom

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 8,916,622
App. No.
13/515,365
Granted
Dec 23, 2014
Kind
B2
Abstract

A heat-curable composition comprises—from 25 to 65% by weight of a mixture of epoxy-functional monomers, said mixture consisting of at least one polyfunctional epoxy monomer selected from monomers comprising from 4 to 8 glycidyl groups and/or cycloaliphatic epoxy groups, and at least one bi- or tri-functional epoxy monomer selected from monomers comprising two or three glycidyl groups and/or cycloaliphatic epoxy groups, —from 25 to 70% by weight of at least one organic solvent selected from glycol monoethers, —from 2.5 to 5% by weight, relative to the total weight of epoxyfunctional monomers (a) and (b), of at least one blocked strong acid catalyst, said heat-curable composition not containing any non-epoxyfunctional monomers, in particular not containing any acrylic, methacrylic or silane monomers.

Claims (15)

1. Heat-curable composition comprising,

from 25 to 65% by weight, relative to the total weight of the composition, of a mixture of epoxy-functional monomers, said mixture consisting of

(a) at least one polyfunctional epoxy monomer selected from monomers comprising from 4 to 8, glycidyl groups and/or cycloaliphatic epoxy groups, which represent from 76 to 85% by weight of total epoxy content,

(b) at least one tri-functional epoxy monomer selected from monomers comprising three glycidyl groups, which represent the balance of total epoxy content,

from 25 to 70% by weight, relative to the total weight of the composition of at least one organic solvent selected from glycol monoethers,

from 2.5 to 5% by weight, relative to the total weight of epoxy functional monomers (a) and (b), of at least one strong acid catalyst which is inactive at ambient temperature (20° C.) and catalyzes epoxy ring-opening only when being heated to a temperature of at least 80° C.,

said heat-curable composition not containing any acrylic, methacrylic or silane monomers.

2. Heat-curable composition according to claim 1 , further comprising from 0.05 to 0.20% by weight of at least one surface agent, said surface agent preferably being selected from fluorocarbon-modified polysiloxanes.

3. Heat-curable composition according to claim 1 , wherein the glycol monoether solvent is selected from alkylene glycol C 1-4 alkyl monoethers.

4. Heat-curable composition according to claim 3 , wherein the glycol monoether is propylene glycol methyl ether (1-methoxy-2-propanol).

5. Heat-curable composition according to claim 1 , containing less than 15% by weight, of additional solvents.

6. Heat-curable composition according to claim 1 , wherein the polyfunctional epoxy monomer (a) is selected from the group consisting of diglycerol tetraglycidyl ether, dipentaerythritol tetraglycidyl ether, sorbitol polyglycidyl ether, polyglycerol polyglycidyl ether, pentaerythritol polyglycidyl ether such as pentaerythritol tetraglycidyl ether.

7. Heat-curable composition according to claim 1 , wherein the polyfunctional epoxy monomer is a hexafunctional glycidyl monomer.

8. Heat-curable composition according to claim 7 , wherein the polyfunctional epoxy monomer (a) is sorbitol polyglycidyl ether.

9. Heat-curable composition according to claim 1 , wherein the bi- or tri-functional epoxy monomer is selected from the group consisting of trimethylolethane triglycidyl ether, trimethylolmethane triglycidyl ether, trimethylolpropane triglycidyl ether, triphenylolmethane triglycidyl ether, trisphenol triglycidyl ether, tetraphenylol ethane triglycidyl ether, p-aminophenol triglycidyl ether, 1,2,6-hexanetriol triglycidyl ether, glycerol triglycidyl ether, diglycerol triglycidyl ether, glycerol ethoxylate triglycidyl ether, Castor oil triglycidyl ether, propoxylated glycerine triglycidyl ether, and mixtures thereof.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 6, 2018
From: ESSILOR INTERNATIONAL (COMPAGNIE GÉNÉRALE D'OPTIQUE)
To: ESSILOR INTERNATIONAL
Reel/Frame 045853/0275 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 24, 2012
From: VALERI, ROBERT
To: ESSILOR INTERNATIONAL (COMPAGNIE GENERALE D'OPTIQUE)
Reel/Frame 028842/0174 →