IP Library Granted Patent US 9,981,453
Granted Patent B2
US 9,981,453 · App. 15/256,202 · Granted May 29, 2018

Photochromic polyurethane laminate

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Quick Facts
Patent No.
US 9,981,453
App. No.
15/256,202
Granted
May 29, 2018
Kind
B2
Abstract

A photochromic polyurethane laminate that is constructed to solve certain manufacturing difficulties involved in the production of plastic photochromic lenses is disclosed. The photochromic laminate includes at least two layers of a resinous material and a photochromic polyurethane layer that is interspersed between the two resinous layers and which contains photochromic compounds. The polyurethane layer is formed by curing a mixture of a solid thermoplastic polyurethane, at least one isocyanate prepolymer, at least one photochromic compound, and a stabilizing system.

Claims (27)

1. A process for producing a transparent photochromic polyurethane laminate, comprising:

a) preparing a solvent casting solution by dissolving a solid thermoplastic polyurethane, at least one isocyanate polyurethane prepolymer, and at least one photochromic compound in a solvent;

b) casting the solution on a first transparent resin sheet to form a cast film;

c) evaporating the solvent from the cast film to a substantially dry state to form a photochromic polyurethane film;

d) laminating the photochromic polyurethane film to a second transparent resin sheet to form a photochromic polyurethane laminate; and

e) curing the photochromic polyurethane laminate.

2. The process according to claim 1 wherein steps b) through d) are carried out through a sequential process.

3. The process according to claim 1 wherein step a) comprises dissolving a solid thermoplastic polyurethane having a molecular weight in the range of about 9,000 to 100,000 grams per mole.

4. The process according to claim 1 wherein step a) comprises forming the solid thermoplastic polyurethane by reacting:

a) a polyol selected from a group consisting of polyester polyols and polyether polyols, having a molecular weight in the range of about 500 to 6,000 g/mol, and a functionality of 2;

b) with a diisocyanate in an equivalent ratio of diisocyanate to polyol in the range of about 1.2:1.0 to 8.0:1.0; and

c) with a diol as a chain extender having a molecular weight in the range of about 62 to 499 g/mol;

wherein the theoretical NCO index of the thermoplastic polyurethane is in a range of 90 to 105.

5. The process according to claim 4 wherein the step of forming the solid thermoplastic polyurethane comprises selecting a polyester polyol from a group consisting of polycaprolactone polyol and poly(butylene adipate) polyol.

6. The process according to claim 4 wherein the step of forming the solid thermoplastic polyurethane comprises selecting a polyether polyol from a group consisting of polypropylene glycol and polytetramethylene glycol.

7. The process according to claim 4 wherein the step of forming the solid thermoplastic polyurethane comprises selecting a diisocyanate from a group consisting of hexamethylene diisocyanate, isophorone diisocyanate, cyclohexane diisocyanate, methylcyclohexane diisocyanate, and dicyclohexylmethane diisocyanate.

8. The process according to claim 4 wherein the step of forming the solid thermoplastic polyurethane comprises selecting a diol from a group consisting of propane diol, butane diol, pentane diol, hexane diol, diethylene glycol, dipropylene glycol, and cyclohexane diol.

9. The process according to claim 1 wherein step a) comprises employing an isocyanate polyurethane prepolymer having a molecular weight in the range of about 1,000 to 6,000 grams per mole.

10. The process according to claim 1 wherein the step of preparing a solvent casting solution comprises selecting a photochromic compound from the group consisting essentially of naphtho[2,1b]pyrans and naphtho[1,2b]pyrans.

11. The process according to claim 1 wherein the step of preparing a solvent casting solution comprises combining said solid thermoplastic polyurethane with said isocyanate-terminated polyurethane prepolymer at a ratio in a range of about 9:1 to 1:9, by weight.

12. The process according to claim 1 wherein step c) comprises forming a photochromic polyurethane film having a thickness in a range of about 10 μm to about 100 μm.

13. The process according to claim 1 wherein step a) comprises forming the isocyanate polyurethane prepolymer by reacting:

a) a polyol selected from a group consisting of polyester polyols and polyether polyols, having a molecular weight in a range of about 500 to 3000 g/mol and a functionality of 2;

b) with an aliphatic diisocyanate, a cycloaliphatic diisocyanate, or both, in an equivalent ratio of diisocyanate to polyol in a range of about 1.2:1.0 to 8.0:1.0.

14. The process according to claim 13 wherein the step of forming the isocyanate polyurethane prepolymer comprises selecting a polyester polyol from a group consisting of polycaprolactone polyol and poly(butylene adipate) polyol.

15. The process according to claim 13 wherein the step of forming the isocyanate polyurethane prepolymer comprises selecting a polyether polyol from a group consisting of polypropylene glycol and polytetramethylene glycol.

16. The process according to claim 13 wherein the step of forming the isocyanate polyurethane prepolymer comprises selecting a diisocyanate from a group consisting of hexamethylene diisocyanate, isophorone diisocyanate, cyclohexane diisocyanate, methylcyclohexane diisocyanate, and dicyclohexylmethane diisocyanate.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 29, 2022
From: VISION EASE, LP
To: HOYA OPTICAL LABS OF AMERICA, INC.
Reel/Frame 059825/0497 →