Retroreflective articles with wash durable bead bond layers

Patent metadata

Field	Value
Publication number	US-10261222-B2
Application number	US-201515319007-A
Country	US
Kind code	B2
Filing date	Jun 10, 2015
Priority date	Jun 16, 2014
Publication date	Apr 16, 2019
Grant date	Apr 16, 2019

Abstract

Retroreflective articles include a layer of optical elements, and a polyurethane bead bond layer. The optical elements include transparent microspheres, and at least one reflective layer. The polyurethane bead bond layer is the reaction product of a reaction mixture of at least one aliphatic polycarbonate polyol and at least one polyisocyanate, and the reaction mixture is free of polyols containing unsaturated groups. The retroreflective articles have improved wash durability.

First claim

What is claimed is:

1. A retroreflective article comprising:
a polyurethane bead bond layer; and
a layer of optical elements partially embedded in the bead bond layer, the optical elements comprising:
transparent microspheres, and at least one reflective layer;

wherein the polyurethane bead bond layer comprises the reaction product of a reaction mixture comprising at least one aliphatic polycarbonate polyol and at least one polyisocyanate, and wherein the reaction mixture is free of polyols containing unsaturated groups, wherein the at least one aliphatic polycarbonate polyol is described by Formula 1:
HO—[(CH 2 ) 2 CHR 1 (CH 2 ) n —O—(CO)—O—] m —[(CH 2 ) 2 CHR 1 (CH 2 ) n ]—OH   Formula 1

wherein (CO) defines a carbonyl group C═O;
R 1 is hydrogen or methyl;
n is an integer of 2 or 3, such that n is 3 when R 1 is hydrogen, and n is 2 when R 1 is methyl; and
m is number in the range 3-23.

2. The retroreflective article of claim 1 , wherein the reaction mixture further comprises at least one additional polyol.

3. The retroreflective article of claim 1 , wherein the reaction mixture further comprises at least two additional polyols.

4. The retroreflective article of claim 3 , wherein at least one of the two additional polyols comprises a polyol with a functionality greater than 2, and wherein at least one of the two additional polyols is not a polyester polyol.

5. The retroreflective article of claim 1 , wherein the at least one polyisocyanate comprises an aliphatic polyisocyanate.

6. The retroreflective article of claim 1 , wherein the at least one polyisocyanate comprises an aromatic polyisocyanate.

7. The retroreflective article of claim 1 , wherein the amount of polyisocyanate present in the reaction mixture comprises a stoichiometric excess of polyisocyanate relative to amount of polyol.

8. The retroreflective article of claim 1 , wherein the reaction mixture further comprises at least one silane coupling agent.

9. The retroreflective article of claim 1 , wherein the reaction mixture further comprises at least one curing catalyst.

10. The retroreflective article of claim 1 , wherein the article is wash durable.

11. The retroreflective article of claim 1 , further comprising a support layer attached to the polyurethane bead bond layer, the support layer comprising a layer of adhesive, a film layer, a fabric layer, or a non-woven layer.

12. An article of clothing comprising:
a fabric with a first major surface and a second major surface; and
a retroreflective appliqué attached to the first major surface of the fabric, the retroreflective appliqué comprising:
a polyurethane bead bond layer;
a layer of optical elements partially embedded in the bead bond layer, the optical elements comprising:
transparent microspheres, and at least one reflective layer;

wherein the polyurethane bead bond layer comprises the reaction product of at least one aliphatic polycarbonate polyol and at least one polyisocyanate, wherein the reaction mixture is free of polyols containing unsaturated groups, wherein the at least one aliphatic polycarbonate polyol is described by Formula 1:
HO—[(CH 2 ) 2 CHR 1 (CH 2 ) n —O—(CO)—O—] m —[(CH 2 ) 2 CHR 1 (CH 2 ) n ]—OH   Formula 1

wherein (CO) defines a carbonyl group C═O;
R 1 is hydrogen or methyl;
n is an integer of 2 or 3, such that n is 3 when R 1 is hydrogen, and n is 2 when R 1 is methyl; and
m is number in the range 3-23; and
a support layer attached to the polyurethane bead bond layer, the support layer comprising a layer of adhesive, a film layer, a fabric layer, or a non-woven layer, wherein the support layer is attached to the first major surface of the fabric.

13. A method of preparing an article comprising:
providing a polymeric carrier layer with a first major surface and a second major surface;
providing transparent microspheres;
partially embedding the transparent microspheres into the first major surface of the polymeric carrier layer such that the beads at least partially protrude from the first major surface of the polymeric carrier layer to form a layer of microspheres;
depositing one or more reflective layers on at least a portion of the first major surface of the polymeric carrier layer and the layer of microspheres;
providing a reaction mixture comprising at least one aliphatic polycarbonate polyol and at least one polyisocyanate, and wherein the reaction mixture is free of polyols containing unsaturated groups, wherein the at least one aliphatic polycarbonate polyol is described by Formula 1:
HO—[(CH 2 ) 2 CHR 1 (CH 2 ) n —O—(CO)—O—] m —[(CH 2 ) 2 CHR 1 (CH 2 ) n ]—OH   Formula 1

wherein (CO) defines a carbonyl group C═O;
R 1 is hydrogen or methyl;
n is an integer of 2 or 3, such that n is 3 when R 1 is hydrogen, and n is 2 when R 1 is methyl; and
m is number in the range 3-23;
applying the reaction mixture to the layer of microspheres; and
curing the reaction mixture to form a polyurethane bead bond layer.

14. The method of claim 13 , wherein the amount of polyisocyanate present in the reaction mixture comprises a stoichiometric excess of polyisocyanate relative to amount of polyol.

15. The method of claim 13 , wherein the reaction mixture further comprises at least one silane coupling agent.

16. The method of claim 13 , wherein the reaction mixture further comprises at least one curing catalyst.

17. The method of claim 13 , further comprising attaching a support layer to the polyurethane bead bond layer, wherein the support layer comprises a layer of adhesive, a film layer, a fabric layer, or a non-woven layer.

18. The method of claim 17 , wherein attaching the support layer to the polyurethane bead bond layer comprises contacting the support layer to the polyurethane bead bond layer prior to curing of the reaction mixture to form the polyurethane bead bond layer.

19. The method of claim 17 , wherein attaching the support layer to the polyurethane bead bond layer comprises adhesively bonding the support layer to the polyurethane bead bond layer after curing of the reaction mixture to form the polyurethane bead bond layer.

20. The method of claim 13 , further comprising removing the polymeric carrier layer to generate a retroreflective article.

21. The method of claim 20 , further comprising adhering the article to a substrate prior to removing the polymeric carrier layer.

Assignees

• 3M Innovative Properties Co

Inventors

• Edwards Bruce H
• Niwas Shri
• Xia Ying

Classifications

• C08G18/44

  Polycarbonates · CPC title

• C08G18/222

  metal compounds not provided for in groups C08G18/225 - C08G18/26 · CPC title

• B05D5/06

  to obtain multicolour or other optical effects (B05D5/02 takes precedence) · CPC title

• C23C14/20

  on organic substrates · CPC title

• C08G18/3215

  containing aromatic groups or benzoquinone groups · CPC title