US2018112102A1PendingUtilityA1
Coating compositions for packaging articles and methods of coating
Est. expiryApr 16, 2030(~3.8 yrs left)· nominal 20-yr term from priority
Inventors:Richard H. EvansJeffrey NiederstRobert M. O'BrienBenoit ProuvostKevin RomagnoliGrant SchuttePaul StensonTom Van Kuren
C09D 5/08C09D 171/08B05D 2518/00B65D 25/34B05D 7/14C08G 59/24C09D 171/12Y10T428/1355B05D 3/007C09D 171/00B05D 7/227C08G 59/066B05D 7/24B65D 25/00B21D 31/00
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Claims
Abstract
This invention provides a polymer that is useful in a variety of applications, including as a binder polymer of a coating composition, and especially a packaging coating composition. Packaging articles (e.g., containers) comprising the polymer and methods of making such packaging articles are also provided.
Claims
exact text as granted — not AI-modified1 - 25 . (canceled)
26 . A food or beverage can coating composition that includes:
a polyether polymer having a backbone that includes a polycyclic group; and a carrier liquid; wherein the coating composition is at least substantially free of bisphenol A and the diglycidyl ether of bisphenol A and is suitable for use in forming a food-contact coating.
27 . The coating composition of claim 26 , wherein the backbone includes —CH 2 —CH(OH)—CH 2 — segments.
28 . The coating composition of claim 26 , wherein the polyether polymer includes one or more of the following segments of Formula I:
—O—Ar—(R n —Ar) n —O—, (I)
wherein:
each Ar is independently an aryl or heteroaryl group,
each n is independently 0 or 1,
R, if present, is a divalent organic group, and
the two oxygen atoms are each ether oxygen.
29 . The coating composition of claim 28 , wherein n is 0.
30 . The coating composition of claim 28 , wherein each n is 1 and R includes the polycyclic group.
31 . The coating composition of claim 26 , wherein the polyether polymer has a Tg of at least 30° C.
32 . The coating composition of claim 26 , wherein the polyether polymer has a number average molecular weight of at least 2,000.
33 . The coating composition of claim 26 , wherein the polyether polymer is a reaction product of ingredients including a polyepoxide and a polyhydric phenol.
34 . The coating composition of claim 33 , wherein one or both of the polyepoxide or polyhydric phenol is derived from isosorbide.
35 . The coating composition of claim 26 , wherein the polyether polymer is a reaction product of ingredients including a diepoxide and a dihydric phenol, and wherein one or both of the diepoxide and the diphenol includes a polycyclic group.
36 . The coating composition of claim 26 , wherein the polycyclic group comprises a bicyclic group.
37 . The coating composition of claim 36 , wherein the bicyclic group is a saturated bicyclic group.
38 . The coating composition of claim 36 , wherein the bicyclic group comprises a tricyclic or higher group.
39 . The coating composition of claim 38 , wherein the tricyclic or higher group comprises a tricyclodecane group.
40 . The coating composition of claim 26 , wherein the polycyclic group comprises an isosorbide group.
41 . The coating composition of claim 26 , wherein the coating composition is a water-based system, and wherein the polyether polymer constitutes at least 10 wt-% of the total resin solids in the coating composition.
42 . The coating composition of claim 26 , wherein the coating composition includes a crosslinker.
43 . The coating composition of claim 42 , wherein the crosslinker comprises a phenoplast.
44 . The coating composition of claim 26 , wherein the backbone includes a plurality of polycyclic groups.
45 . The coating composition of claim 44 , wherein the polyether polymer includes one or more pendant hydroxyl groups attached to backbone carbon atoms.
46 . The coating composition of claim 44 , wherein the polyether polymer has a Tg of at least 70° C.
47 . The coating composition of claim 44 , wherein the polyether polymer has a Tg from about 80° C. to about 110° C.
48 . The coating composition of claim 44 , wherein the polyether polymer is a reaction product of ingredients including a diepoxide and a dihydric phenol.
49 . The coating composition of claim 44 , wherein the coating composition is a solvent-based system, and wherein the polyether polymer constitutes at least 30 wt-% of the total resin solids in the coating composition.
50 . A metal food or beverage can or a portion thereof having a food-contact coating formed from the coating composition of claim 26 .
51 . A food or beverage can coating composition that includes:
a polyether polymer formed form ingredients including a diepoxide and a diphenol, wherein the diepoxide is derived from isosorbide; and a carrier liquid; wherein the coating composition is at least substantially free of bisphenol A and the diglycidyl ether of bisphenol A and is suitable for use in forming a food-contact coating.
52 . The coating composition of claim 51 , wherein the polyether polymer has a Tg of at least 70° C.
53 . A metal food or beverage can or a portion thereof having a food-contact coating formed from the coating composition of claim 51 .
54 . A method, including:
applying a coating composition on at least a portion of a surface of a metal substrate prior to, or after, forming the substrate into a food or beverage container or a portion thereof; wherein the coating composition is at least substantially free of bisphenol A and the diglycidyl ether of bisphenol A and comprises:
a polyether polymer having a backbone that includes a polycyclic group; and
a carrier liquid.
55 . The method of claim 54 , wherein the polycyclic group comprises a tricyclodecane group.
56 . The method of claim 54 , wherein the polycyclic group comprises an isosorbide group.
57 . The method of claim 54 , wherein the coating composition is applied to the metal substrate after forming the substrate into a food or beverage container or a portion thereof.Cited by (0)
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