IP Library Granted Patent US 9,181,460
Granted Patent B2
US 9,181,460 · App. 13/787,154 · Granted Nov 10, 2015

Gas transmitting polyurethane adhesive

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Quick Facts
Patent No.
US 9,181,460
App. No.
13/787,154
Granted
Nov 10, 2015
Kind
B2
Abstract

A two-part, solvent-free laminating adhesive including a Part A that is a liquid mixture of a first polyol and a hydroxyl functional acrylic polymer having a molecular weight of no greater than 15,000 g/mole, and a Part B that is an isocyanate-terminated polyurethane prepolymer. The adhesive is especially suited for making flexible laminates for use in food packaging. When adhered two polymeric film materials and in cured form, the adhesive provides substantially no contribution to the oxygen barrier properties of the laminate.

Claims (33)

1. A two-part solvent-free laminating adhesive for a laminate, comprising Part (A), a mixture of

i) from about 20% by weight to about 80% by weight of a first polyol selected from the group consisting of polyether polyols, polyester polyols, polyester/polyether polyols, natural oil polyols, and combinations thereof, and

ii) from about 20% by weight to about 80% by weight of a hydroxyl functional acrylic polymer having a weight average molecular weight of no greater than 15,000 g/mole, a glass transition temperature (Tg) of no greater than 20° C., and a hydroxyl number of from about 10 to about 110, the first polyol and the hydroxyl functional acrylic polymer being co-dissolved so as to form a homogeneous liquid solution, and

Part (B), an isocyanate-terminated polyurethane prepolymner having a percentage isocyanate (NCO%) of from about 4% to about 20% based on the weight of the prepolymer, the Part (B) being present relative to the Part (A) at an NCO/OH ratio of at least about 1.1,

wherein the laminate exhibits an oxygen transmission rate (OTR) percent decrease of no greater than 7% according to the OTR Percent Decrease Determination Method.

2. The adhesive of claim 1 , wherein the first polyol in Part (A) is a polyether polyol having a number average molecular weight of no less than 1,000 g/mole.

3. The adhesive of claim 1 , wherein the natural oil polyols in Part (A) are selected from the group consisting of soybean oil polyol, castor oil polyol, rapeseed oil polyol, and hydroxyl functional compounds that are isolated from, derived from or manufactured from animal oils and vegetable oils, and combinations thereof.

4. The adhesive of claim 1 , wherein the first polyol in Part (A) is a castor oil polyol.

5. The adhesive of claim 1 , wherein the first polyol in Part (A) is a combination of a polyether polyol having a number average molecular weight of no less than 1,000 g/mole and a castor oil polyol.

6. The adhesive of claim 1 , wherein the hydroxyl functional acrylic polymer in Part (A) has a weight average molecular weight of from about 2000 g/mole to about 10,000 g/mole, and a hydroxyl number of from about 50 to about 90.

7. The adhesive of claim 1 , wherein the isocyanate-tenninated polyurethane prepolymer in Part (B) is a reaction product of the first polyol and a polyisocyanate at an NCO/OH ratio of from about 2:1 to about 8:1, wherein the polyisocyanate is selected from a group consisting of a diphenylmethane diisocyanate and its isomers; toluene diisocyanate; a modified diphenylmethane diisocyanate selected from the group consisting of a carbodiimide-modified diphenylmethane diisocyanate, an allophanate-modified diphenylmethane diisocyanate, a biuret-modified diphenylmethane diisocyanate, a polymeric diphenylmethane diisocyanate; and combinations thereof.

8. The adhesive of claim 7 , wherein the first polyol is a polyether polyol having a number average molecular weight of no less than 1,000 g/mole and the polyisocyanate is a carbodiimide-modified diphenylmethane diisocyanate.

9. The adhesive of claim 7 , wherein the first polyol is a combination of a polyether polyol having a number average molecular weight of no less than 1,000 g/mole and a castor oil polyol, and the polyisocyanate is a carbodiimide-modified diphenylmethane diisocyanate.

10. A method of making a laminate that comprises a first substrate and a second substrate, the method comprising

applying a two-part solvent-free adhesive of claim 1 to a surface of the first substrate to form an adhesive bearing surface of the first substrate, and

contacting a surface of the second substrate with the adhesive bearing surface of the first substrate to form the laminate.

11. The method of claim 10 , wherein the first and the second substrates are the same or different film material, each exhibiting an oxygen transmission rate (OTR) of at least about 300 cc/(100 in 2 -day) when tested according to the herein described OTR Test Method, and each being selected from the group consisting of polyethylene, polypropylene, paper, and laminates thereof.

12. The method of claim 10 , wherein the first polyol in Part (A) of the adhesive is a combination of a polyether polyol having a number average molecular weight of no less than 1,000 g/mole and a castor oil polyol.

13. The method of claim 10 , wherein the isocyanate-terminated polyurethane prepolymer of Part (B) is a reaction product of the first polyol and carbodiimide-modified diphenylmethane diisocyanate, the first polyol being a combination of a polyether polyol having a number average molecular weight of no less than 1,000 g/mole and a castor oil polyol.

14. A laminate, comprising

a first and a second substrates adhered by the adhesive of claim 1 .

15. The laminate of claim 14 , wherein the first and the second substrates are the same or different film material, each exhibiting an oxygen transmission rate (OTR) of at least about 300 cc/(100 in 2 -day), when tested according to the herein described OTR Test Method, and each being selected from the group consisting of polyethylene, polypropylene, paper, and laminates thereof.

16. The laminate of claim 14 , wherein the first polyol in Part (A) of the adhesive is a polyether polyol having a number average molecular weight of no less than 1,000 g/mole.

17. The laminate of claim 14 , wherein the first polyol in Part (A) of the adhesive is a combination of a polyether polyol having a number average molecular weight of no less than 1,000 g/mole and a castor oil polyol.

18. The laminate of claim 14 , wherein the isocyanate-terminated polyurethane prepolymer in Part (B) of the adhesive is a reaction product of the first polyol and carbodiimide-modified diphenylmethane diisocyanate, the first polyol being a combination of a polyether polyol having a number average molecular weight of no less than 1,000 g/mole and a castor oil polyol.

19. A packaged food article, comprising

a laminate of claim 14 in a form of a food package, and

a food product contained inside of the food package.

20. A two-part solvent-free laminating adhesive for a laminate, comprising Part (A), a mixture of

i) from about 20% by weight to about 80% by weight of a first polyol selected from the group consisting of polyether polyols, polyester polyols, polyester/polyether polyols, natural oil polyols, and combinations thereof, and

ii) from about 20% by weight to about 80% by weight of a hydroxyl functional acrylic polymer having a weight average molecular weight of no greater than 15,000 g/mole, a glass transition temperature (Tg) of no greater than 20° C., and a hydroxyl number of from about 10 to about 110, the first polyol and the hydroxyl functional acrylic polymer being co-dissolved so as to form a homogeneous liquid solution, and

Part (B), an isocyanate-terminated polyurethane prepolymer that is a reaction product of a polyol and a polyfunctional isocyanate selected from a group consisting of 4,4′-diphenylmethane diisocyanate (MDI) and its isomers, toluene diisocyanate (TDI), hexamethylene diisocyanate, isophorone diisocyanate, tetramethylxylene diisocyanate, modified diphenylmethane diisocyanate including carbodiimide-modified diphenylmethane diisocyanate, allophanate-modified diphenylmethane diisocyanate, biuret-modified diphenylmethane diisocyanate, and polymeric diphenylmethane diisocyanate, and combinations thereof, the Part (B) being present relative to the Part (A) at an NCO/OH ratio of at least about 1.1,

wherein the laminate exhibits an oxygen transmission rate (OTR) percent decrease of no greater than 7% according to the OTR Percent Decrease Determination Method.

Assignments (4)
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS (TERM LOAN) Recorded Feb 15, 2023
From: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
To: H.B. FULLER COMPANY; H.B. FULLER CONSTRUCTION PRODUCTS INC.; ROYAL ADHESIVES AND SEALANTS, LLC; ADCO PRODUCTS, LLC
Reel/Frame 062761/0884 →
TERM LOAN SECURITY AGREEMENT Recorded Oct 25, 2017
From: H.B. FULLER COMPANY; H.B. FULLER CONSTRUCTION PRODUCTS INC.; ROYAL ADHESIVES AND SEALANTS, LLC; ADCO PRODUCTS, LLC
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 044616/0671 →
RCF SECURITY AGREEMENT Recorded Oct 25, 2017
From: H.B. FULLER COMPANY; H.B. FULLER CONSTRUCTION PRODUCTS INC.; ROYAL ADHESIVES AND SEALANTS, LLC; ADCO PRODUCTS, LLC
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 044616/0700 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 6, 2013
From: EKLUND, WAYNE G.; RIPPE, STEPHEN G.
To: H.B. FULLER COMPANY
Reel/Frame 029934/0581 →