IP Library Granted Patent US 9,472,126
Granted Patent B2
US 9,472,126 · App. 14/523,380 · Granted Oct 18, 2016

Pressure sensitive adhesive compositons

Inventors: Andrew LaChapell (Taylors, SC); Jong Guo (Charlotte, NC)
Assignee: SYNTHOMER USA LLC
G09F3/10C09J7/0217C09J133/26C09J2201/622C09J2433/003
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Quick Facts
Patent No.
US 9,472,126
App. No.
14/523,380
Granted
Oct 18, 2016
Kind
B2
Abstract

Disclosed are removable pressure sensitive adhesive compositions (PSAs) useful with facestocks and/or packaging labels designed to be removed in the recycling of polymeric packaging. The PSAs of the invention include (a) at least one monomer which may undergo free radical polymerization and whose homopolymer has a glass transition temperature of less than or equal to 10° C., (b) at least one mono-olefinically unsaturated monomer having aldehyde or ketone functionality, and (c) an effective amount of at least one polyhydrazide crosslinker having hydrazine functionality. The PSA composition of the invention exhibits a peel adhesion value of between about 0.4 lbs/in (70 N/m) and about 4 lbs/in (700 N/m), and the percent film remaining on the polymeric packaging after a sink-float testing is 0% to about 8%.

Claims (30)

1. A filmic facestock material for polymeric packaging comprising:

a pressure sensitive adhesive composition comprising a monomer mixture, wherein the monomer mixture comprises (a) at least one monomer that is free radical polymerizable and whose homopolymer has a glass transition temperature of less than or equal to 10° C., (b) greater than 0.1 wt. % to 1 wt. % based on the weight of the monomer mixture of at least one mono-olefinically unsaturated monomer having aldehyde or ketone functionality, and (c) at least one polyhydrazide crosslinker having hydrazine functionality;

wherein the pressure sensitive adhesive composition exhibits a peel adhesion value of between about 0.4 lbs/in (70 N/m) and about 4 lbs/in (700 N/m); and

wherein a percent film remaining on the polymeric packaging after a sink-float testing is 0% to about 8%.

2. The filmic facestock material of claim 1 wherein the at least one monomer that is free radical polymerizable and whose homopolymer has a glass transition temperature of less than or equal to 10° C. comprises at least one acrylic acid ester or (meth)acrylate acid ester.

3. The filmic facestock material of claim 2 wherein the least one acrylic acid ester or (meth)acrylate acid ester is selected from the group consisting of benzyl acrylate, n-butyl acrylate, sec-butyl acrylate, cyanoethyl acrylate, iso-decyl acrylate, n-decyl acrylate, dodecyl acrylate, dodecyl methacrylate, 2-ethoxyethyl acrylate, ethyl acrylate, 2-ethylhexyl acrylate, 2-ethylhexyl methacrylate, n-hexyl acrylate, hexyl methacrylate, isobutyl acrylate, isopropyl acrylate, isotactic, 2-methoxyethyl acrylate, methyl acrylate, octadecyl methacrylate, octyl methacrylate, 2-phenylethyl acrylate, n-propyl acrylate, and 2,2,2-trifluoroethyl acrylate, and combinations thereof.

4. The filmic facestock material of claim 3 wherein the least one acrylic acid ester or (meth)acrylate acid ester is selected from the group consisting of 2-ethylhexyl acrylate, n-butyl acrylate, and combinations thereof.

5. The filmic facestock material of claim 1 wherein the at least one at least one mono-olefinically unsaturated monomer having an aldehyde or ketone functionality is selected from the group consisting of acrolein, methacrolein, vinylbenzaldehyde, crotonaldehyde, (meth)acryloxyalkylpropanals, diacetone acrylamide, diacetone acrylate, and combinations thereof.

6. The filmic facestock material of claim 5 wherein the at least one at least one mono-olefinically unsaturated monomer having an aldehyde or ketone functionality is selected from the group consisting of diacetone acrylamide, diacetone acrylate, acrolein, and combinations thereof.

7. The filmic facestock material of claim 1 wherein the monomer mixture comprises: 50 wt % to about 95 wt % of the at least one monomer which may undergo free radical polymerization and whose homopolymer has a glass transition temperature of less than or equal to 10° C., and greater than 0.1 wt. % to 1 wt. % of the at least one mono-olefinically unsaturated monomer having an aldehyde or ketone group, wherein the wt % is based on the weight of the monomer mixture.

8. The filmic facestock material of claim 1 wherein the monomer mixture further comprises one or more ethylenically unsaturated carboxylic acid.

9. The filmic facestock material of claim 1 wherein the monomer mixture further comprises at least one monomer that is free radical polymerizable and whose homopolymer has a glass transition temperature of greater than 10° C.

10. The filmic facestock material of claim 1 wherein the hydrazine functionality is between about 0.02 to 5 equivalents per 1 equivalent of the aldehyde or ketone functionality.

11. The filmic facestock material of claim 1 wherein the polyhydrazide is selected from the group consisting of oxalic acid dihydrazide, malonic acid dihydrazide, succinic acid dihydrazide, glutaric acid dihydrazide; adipic acid dihydrazide, sebacic acid dihydrazide; monoolefin unsaturated dicarboxylic acid dihydrazide such as maleic acid dihydrazide, fumaric acid dihydrazide, itaconic acid dihydrazide; carbonic acid 10 polyhydrazide such as carbonic acid dihydrazide; aromatic dihydrazides such as phthalic acid dihydrazide, terephthalic acid dihydrazide, isophthalic acid dihydrazide; trihydrazides such as 1,2,4-butanetricarbohydrazide, 1,1,4-butanetricarbohydrazide,1,2,5-pentanetricarbohydrazide, 1,3,6-hexanetricarbohydrazide, 1,3,7-heptanetricarbohydrazide, and I-hydroxy-1,2,4-butanetricarbohydrazide, and combinations thereof.

12. The filmic facestock material of claim 11 wherein polyhydrazide is selected from the group consisting of adipic dihydrazide, isophthalic dihydrazide, sebacic dihydrazide, bis-semicarbizides, and combinations thereof.

13. The filmic facestock material of claim 1 wherein the polymeric packaging comprises polyethylene teraphthalate, high density polyethylene, polyvinyl chloride, polypropylene or combinations thereof.

14. The filmic facestock material of claim 1 wherein the filmic facestock comprises an olefinic facestock, a polystyrene facestock, a polyethylene teraphthalate facestocks, a polyvinyl chloride or combinations thereof.

15. The filmic facestock material of claim 1 wherein the pressure sensitive adhesive composition further comprises a surfactant with a reactive carbon-carbon double bond.

16. The filmic facestock material of claim 15 wherein the surfactant with a reactive carbon-carbon double bond is selected from the group consisting of alkylphenol ethoxylates containing alkenyl substituents, polyoxyalkylene-1-(allyloxymethyl) alkyl ether sulfate salt compounds, salts of poly(oxy-1,2-ethanediyl), alpha-sulfo-omega-[1-(hydroxymethyl)-2-(2-propen-yloxy)ethoxy] and combinations thereof.

17. The filmic facestock material of claim 1 wherein the facestock material is an olefinic facestock.

18. A filmic facestock material for polymeric packaging comprising:

a pressure sensitive adhesive composition comprising a monomer mixture, wherein the monomer mixture comprises (a) at least one monomer that is free radical polymerizable and whose homopolymer has a glass transition temperature of less than or equal to 10° C., (b) greater than 0.1 wt. % to 1 wt. % based on the weight of the monomer mixture of at least one mono-olefinically unsaturated monomer having aldehyde or ketone functionality, and (c) at least one polyhydrazide crosslinker having hydrazine functionality, and a surfactant with a reactive carbon-carbon double bond;

wherein the pressure sensitive adhesive composition exhibits a peel adhesion value of between about 0.4 lbs/in (70 N/m) and about 4 lbs/in (700 N/m); and

wherein a percent film remaining on the polymeric packaging after a sink-float testing is 0% to about 8%.

19. A filmic facestock material for polymeric packaging comprising:

a pressure sensitive adhesive composition comprising a monomer mixture, wherein the monomer mixture comprises (a) 50 wt % to about 95 wt % of at least one monomer that is free radical polymerizable and whose homopolymer has a glass transition temperature of less than or equal to 10° C., (b) greater than 0.1 wt. % to 1 wt % at least one mono-olefinically unsaturated monomer having aldehyde or ketone functionality, (c) at least one polyhydrazide crosslinker having hydrazine functionality, and a surfactant with a reactive carbon-carbon double bond, where the wt % is based on the weight of the monomer mixture;

wherein the hydrazine functionality is between about 0.02 to 5 equivalents per 1 equivalent of the aldehyde or ketone functionality;

wherein the pressure sensitive adhesive composition exhibits a peel adhesion value of between about 0.4 lbs/in (70 N/m) and about 4 lbs/in (700 N/m); and

wherein a percent film remaining on the polymeric packaging after a sink-float testing is 0% to about 8%.

20. The filmic facestock material of claim 19 wherein the surfactant with a reactive carbon-carbon double bond is selected from the group consisting of alkylphenol ethoxylates containing alkenyl substituents, polyoxyalkylene-1-(allyloxymethyl) alkyl ether sulfate salt compounds, salts of poly(oxy-1,2-ethanediyl), alpha-sulfo-omega-[1-(hydroxymethyl)-2-(2-propen-yloxy)ethoxy] and combinations thereof.

Assignments (10)
RELEASE OF SECURITY INTEREST Recorded Feb 23, 2017
From: WILMINGTON TRUST, NATIONAL ASSOCIATION
To: HEXION INC. (FORMERLY KNOWN AS MOMENTIVE SPECIALTY CHEMICALS INC.)
Reel/Frame 041793/0881 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 7, 2016
From: HEXION INC.
To: SYNTHOMER USA LLC
Reel/Frame 039662/0102 →
RELEASE OF SECURITY INTEREST Recorded Jul 26, 2016
From: WILMINGTON TRUST, NATIONAL ASSOCIATION
To: HEXION INC.
Reel/Frame 039259/0099 →
RELEASE OF SECURITY INTEREST Recorded Jul 26, 2016
From: WILMINGTON TRUST, NATIONAL ASSOCIATION
To: HEXION INC.
Reel/Frame 039259/0418 →
RELEASE OF SECURITY INTEREST Recorded Jul 26, 2016
From: WILMINGTON TRUST COMPANY
To: HEXION INC.
Reel/Frame 039259/0628 →
SECURITY INTEREST Recorded Feb 16, 2015
From: MOMENTIVE SPECIALTY CHEMICALS INC.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 034967/0872 →
SECURITY INTEREST Recorded Feb 16, 2015
From: MOMENTIVE SPECIALTY CHEMICALS INC.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 034967/0747 →
SECURITY INTEREST Recorded Feb 16, 2015
From: MOMENTIVE SPECIALTY CHEMICALS INC.
To: WILMINGTON TRUST COMPANY, AS COLLATERAL AGENT
Reel/Frame 034967/0794 →
CHANGE OF NAME Recorded Feb 3, 2015
From: MOMENTIVE SPECIALTY CHEMICALS INC.
To: HEXION INC.
Reel/Frame 034882/0131 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 6, 2014
From: LACHAPELL, ANDREW; GUO, JONG
To: MOMENTIVE SPECIALTY CHEMICALS INC.
Reel/Frame 034120/0991 →
Continuity (1)
Related Publication 20160117958A1 · Apr 28, 2016