U.S. patent application number 12/815550 was filed with the patent office on 2010-09-30 for cross-linked polyester protective coatings.
This patent application is currently assigned to VALSPAR SOURCING, INC.. Invention is credited to Fritz Altmann, Peter Mayr, James Robinson.
Application Number | 20100247827 12/815550 |
Document ID | / |
Family ID | 37747876 |
Filed Date | 2010-09-30 |
United States Patent
Application |
20100247827 |
Kind Code |
A1 |
Mayr; Peter ; et
al. |
September 30, 2010 |
Cross-Linked Polyester Protective Coatings
Abstract
The invention relates to protective coating systems derived from
a functional polyester resin, a cross-linker and a
phenol-formaldehyde resin. Also provided is a method of coating a
metal substrate using the protective coating systems to produce a
cross-linked protective coating. Further provided is a composite
material prepared with the coating system and, in certain
embodiments, useful in fabricating metal foodstuffs storage
containers. The composite material may be particularly useful in
fabricating foodstuffs storage containers and "easy-open" end
closures wherein the cross-linked protective coating contacts the
foodstuffs.
Inventors: |
Mayr; Peter; (Laxenberg,
AT) ; Robinson; James; (Pittsburgh, PA) ;
Altmann; Fritz; (Engi, CH) |
Correspondence
Address: |
VALSPAR SOURCING, INC.
901 3rd Avenue South, PO Box 1461
MINNEAPOLIS
MN
55440-1461
US
|
Assignee: |
VALSPAR SOURCING, INC.
Minneapolis
MN
|
Family ID: |
37747876 |
Appl. No.: |
12/815550 |
Filed: |
June 15, 2010 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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11220354 |
Sep 6, 2005 |
7763323 |
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12815550 |
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Current U.S.
Class: |
428/35.8 |
Current CPC
Class: |
C08L 67/00 20130101;
C08L 61/12 20130101; C08L 67/00 20130101; C08L 61/06 20130101; C08G
18/4027 20130101; C09D 175/04 20130101; C08G 18/8074 20130101; C09D
167/00 20130101; C08K 5/0025 20130101; C09D 167/00 20130101; B05D
7/542 20130101; C08G 18/542 20130101; Y10T 428/31786 20150401; Y10T
428/1355 20150115; C08K 5/29 20130101; C08G 2390/40 20130101; C08L
2666/14 20130101; C08L 2666/14 20130101 |
Class at
Publication: |
428/35.8 |
International
Class: |
B32B 1/02 20060101
B32B001/02 |
Claims
1-24. (canceled)
25. An article, comprising: a food or beverage container having at
least one surface of a metal substrate coated with a coating
composition comprising: a hydroxyl-functional polyester resin, a
carboxyl-functional polyester resin, a cross-linker, and one or
more phenol-formaldehyde resin; wherein: the coating composition is
substantially free of BPA, BPF, BADGE and BFDGE, and at least one
of the polyester resins exhibits a glass transition temperature
greater than 50.degree. C.
26. The article of claim 25, wherein at least one of the functional
polyester resins exhibits a glass transition temperature of from
greater than 50.degree. C. to less than about 100.degree. C.
27. The article of claim 25, wherein at least one of the functional
polyester resins exhibits a glass transition temperature of from
greater than 60.degree. C. to less than 90.degree. C.
28. The article of claim 25, wherein each of the
hydroxyl-functional polyester resin and the carboxyl-functional
polyester resin exhibit a glass transition temperature of greater
than 50.degree. C.
29. The article of claim 25, wherein the carboxyl-functional
polyester resin exhibits an acid number from about 100 to about 300
milligrams KOH per gram and the hydroxyl-functional polyester
exhibits a hydroxyl number from about 5 to about 200 milligrams KOH
per gram.
30. The article of claim 25, wherein the hydroxyl-functional
polyester resin exhibits a number average molecular weight from
about 1,000 to about 7,500 Daltons.
31. The article of claim 25, wherein the hydroxyl-functional
polyester resin is present in an amount from about 75 to about 90
percent by weight of the coating composition on a non-volatile
solids basis.
32. The article of claim 25, wherein the carboxyl-functional
polyester resin exhibits a number average molecular weight from
about 2,000 to about 5,000 Daltons.
33. The article of claim 25, wherein the carboxyl-functional
polyester resin is present in an amount from about 0.1 to about 5
percent by weight of the coating composition on a non-volatile
solids basis.
34. The article of claim 25, wherein the coating composition
includes a mixture of the hydroxyl-functional polyester resin and
the carboxyl-functional polyester resin having a weight ratio of
hydroxyl-functional polyester resin to carboxyl-functional
polyester resin of from about 50 to 1 to about 600 to 1 parts by
weight on a non-volatile solids basis.
35. The article of claim 25, wherein the cross-linker comprises a
phenoplast cross-linker, an aminoplast cross-linker, or a blocked
isocyanate cross-linker.
36. The article of claim 25, wherein the cross-linker is a blocked
isocyanate cross-linker present in an amount from 1% to 5% by
weight of the coating composition on a non-volatile solids
basis.
37. The article of claim 25, wherein the coating composition
further comprises a resole-formaldehyde resin.
38. The article of claim 25, wherein the coating composition, on a
non-volatile solids basis, comprises: from 50% to 99% of functional
polyester resin, from 0.5% to 10% of the one or more
phenol-formaldehyde resin, and from 0.1% to 10% of the
cross-linker.
39. The article of claim 25, wherein the coating composition
further comprises a substantially nonaqueous carrier liquid.
40. The article of claim 25, wherein the coating composition
comprises a cured coating.
41. The article of claim 25, wherein the coating composition
comprises at least one layer of a multi-coat coating system.
42. The article of claim 25, wherein an interior surface of the
food or beverage container is coated with the coating
composition.
43. The article of claim 25, wherein the food or beverage container
is a multi-part metal can having at least one easy-open end closure
with at least an interior surface of the easy-open end closure
coated with the coating composition.
44. An article, comprising: a metal food or beverage container
having at least one surface coated with a coating composition
comprising: a hydroxyl-functional polyester resin, a
carboxyl-functional polyester resin having an acid number from
about 100 to about 300 milligrams KOH per gram, a cross-linker, and
one or more phenol-formaldehyde resin; wherein the coating
composition is substantially free of BPA, BPF, BADGE and BFDGE.
Description
TECHNICAL FIELD
[0001] The invention relates to protective coating compositions and
methods for coating metal substrates useful in fabricating, for
example, packaging containers. The invention further relates to
methods for coating cross-linkable compositions on metal substrates
useful in fabricating metal foodstuffs packaging containers and
"easy-open" end closures wherein the protective coating contacts
the foodstuffs.
BACKGROUND
[0002] Protective coatings are applied to the interior of metal
food and beverage containers (e.g. cans) to prevent the contents
from coming into contact with the metal surfaces of the containers.
Contact of the container contents with the interior metal surface,
especially where acidic products such as soft drinks and tomato
juice are involved, can lead to corrosion of the metal container
and result in contamination and deterioration of the contents.
Protective coatings are also applied to the interior of food and
beverage containers to prevent corrosion in the headspace of the
container between the fill line of the food product and the
container lid, which is particularly problematic with high salt
content food products.
[0003] Metal container interiors are typically coated with a thin
thermoset film to protect the interior metal surface from its
contents. Various natural and synthetic resins and their blends
have been used as interior can protective coatings, including
poly(vinyl chloride) resins, epoxy-functional resins,
alkyd/aminoplast resins and oleoresinous materials. These
heat-curable compositions are usually applied as solutions or
dispersions of one or more resin in volatile organic solvents.
[0004] The heat-cured protective coating compositions generally
should exhibit sufficient adhesion and flexibility to maintain film
integrity during container fabrication. Sufficient coating adhesion
and flexibility also are needed for the coating composition to
withstand processing conditions the container is subject to during
product packaging. Other desired performance features of the cured
coatings include corrosion protection and sufficient chemical,
abrasion and mar resistance. The coatings used on the interior of
metal food containers preferably also meet government regulatory
criteria.
[0005] Multi-coat coating systems recently have been used to coat
the interior of food and beverage containers, wherein the over-coat
or lacquer contains an epoxy resin cross-linked with a phenolic
resin. Such epoxy-based "Gold lacquers" typically exhibit good
adhesion and can be used for storing acidic foodstuffs and
beverages. However, there is a perception that some epoxy-based
coatings; containing mobile Bisphenol A (BPA), Bisphenol F (BPF),
Bisphenol A diglycidyl ether (BADGE) and Bisphenol F diglycidyl
ether (BFDGE); are less desirable for foodstuffs storage.
[0006] Currently, the food packaging industry and consumer groups
are seeking coated metal packaging articles prepared from coating
compositions free from mobile BPA, BPF, BADGE and BFDGE; exhibiting
excellent corrosion and chemical resistance; and acceptable
adhesion and flexibility during container fabrication. The art
continues to seek an ideal coating composition for use as a
protective coating for metal foodstuffs containers.
SUMMARY OF THE INVENTION
[0007] The present invention is directed to hardenable protective
coating compositions for coating metal substrates. The present
invention is also directed to protective coating compositions
substantially free of mobile BPA, BPF and BADGE and BFDGE. The
present invention is further directed to methods useful in applying
protective coatings to the interior lining of metal containers
suitable for contact with foodstuffs. For example, an exemplary
cured coating composition of the present invention demonstrates
adequate chemical and physical properties for use as a protective
coating system on the interior of metal containers and "easy open"
end closures used in packaging foods and beverages.
[0008] One aspect of the present invention provides a hardenable
packaging coating composition including a hydroxyl-functional
polyester resin, a carboxyl-functional polyester resin, a
cross-linker and a phenol-formaldehyde resin. In certain presently
preferred embodiments, the hardenable packaging coating composition
is substantially free of mobile BPA, BPF, BADGE and BFDGE.
[0009] In another aspect, the present invention provides a
hardenable packaging coating composition including a functional
polyester resin, a blocked-isocyanate cross-linker and a
phenol-formaldehyde resin. In certain presently preferred
embodiments, the hardenable packaging coating composition includes
at least one of a carboxyl-functional polyester resin and a
hydroxyl-functional polyester resin. In one particular preferred
embodiment, the hardenable packaging coating composition further
includes one or more of a resole-formaldehyde resin, a
substantially nonaqueous carrier liquid, a catalyst, or a
pigment.
[0010] In another aspect, the present invention provides a method
for coating a metal substrate with a hardenable packaging coating
composition according to the present invention. The method includes
applying a first hardenable coating composition to at least one
surface of a metal substrate; applying a second hardenable coating
composition over the first hardenable coating composition, wherein
the second hardenable coating composition includes a
hydroxyl-functional polyester resin, a carboxyl-functional
polyester resin, a cross-linker, and a phenol-formaldehyde resin;
and curing the first and second hardenable coating compositions to
provide a hardened composite coating on the metal substrate.
[0011] In some embodiments, the chemical composition of the first
hardenable coating composition is chemically distinct from the
chemical composition of the second hardenable coating composition.
In one presently preferred embodiment, the first hardenable coating
composition is substantially identical in chemical composition to
the second hardenable coating composition. In other presently
preferred embodiments, each of the first and second hardenable
coating compositions is applied at a coating weight of from about 6
to about 12 grams per square meter on a non-volatile solids
basis.
[0012] In another aspect of the present invention, a metal
foodstuffs container is provided, wherein at least an interior
surface of the container is coated with a hardened packaging
coating composition according to the present invention. Preferably
the metal foodstuffs container is a multi-part can with at least
one "easy-open" end closure having at least an interior surface of
the can and the end closure coated with the hardened packaging
coating compositions according to the present invention.
[0013] The hardened composite packaging coating composition
preferably maintains metal corrosion inhibition, imparts chemical
resistance to foodstuffs exposure, and achieves cured film
integrity with good metal substrate adhesion and flexibility
sufficient for container fabrication. In certain preferred
embodiments, the hardened composite coating composition also
provides improved resistance to acidic foodstuffs, and is
particularly useful in fabricating containers having "easy-open"
end closures.
[0014] The details of one or more embodiments of the invention are
set forth in the following
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
DEFINITIONS
[0015] As used herein, the term "BADGE and BFDGE" denotes compounds
selected from the group consisting of Bisphenol A diglycidyl ether
(BADGE) [2,2'-bis(4-hydroxyphenyl)propane
bis(2,3-epoxypropyl)ether], and Bisphenol F diglycidyl ether
(BFDGE) in both the uncured and cured state.
[0016] The term "substantially free" of a particular mobile
compound means that the compositions of the present invention
contain less than 100 parts per million (ppm) of the recited mobile
compound.
[0017] The term "essentially free" of a particular mobile compound
means that the composition of the present invention contains less
than 5 parts per million of the recited mobile compound.
[0018] The term "completely free" of a particular mobile compound
means that the compositions of the present invention contain less
than 20 parts per billion (ppb) of the recited mobile compound.
[0019] The term "mobile" means that the compound can be extracted
from the cured coating when a coating (typically approximately 1
mg/cm.sup.2 thick) is exposed to a 10 weight percent (i.e. 10% w/w)
ethanol solution for two hours at 121.degree. C. followed by
exposure for 10 days in the solution at 49.degree. C.
[0020] If the aforementioned phrases are used without the term
"mobile" (e.g., "substantially free of BPA, BPF, BADGE and BFDGE")
then the compositions of the present invention contain less than
the aforementioned amount of the compound whether the compound is
mobile in the coating or bound to a constituent of the coating.
[0021] As used herein, the term "multi-coat coating system" is
defined as a coating system requiring the application of at least
two coated layers to a particular substrate surface. The coated
layers may be chemically distinct (e.g. a "two-coat coating system"
using a first-coat composition chemically distinct from the
second-coat composition) or chemically identical (e.g. "a two-pass
coating system" using a first-coat composition that has a chemical
composition substantially identical to the second-coat
composition).
[0022] The term "two-coat coating system" is defined as a
multi-coat coating system in which only two chemically distinct
coating compositions are applied to a particular substrate
surface.
[0023] The term "first-coat composition" is defined as the coating
composition to be applied to the surface of a substrate or between
a surface of a substrate and a "second-coat composition," and is
synonymous with base-coat, primer or size for a two-coat coating
system.
[0024] The term "second-coat composition" is defined as the coating
composition to be applied over an applied first-coat composition,
and is synonymous with top-coat or lacquer for a two-coat coating
system.
[0025] The term "cured coating composition" is defined as the
adherent (co)polymeric coating residing on a substrate resulting
from at least partially curing or hardening a coating composition,
for example, by film formation, cross-linking, and the like.
[0026] The term "coating solids" is defined as including all
non-volatile materials that remain in the "cured coating
composition" on the coated substrate after curing.
[0027] The term "(co)polymer" is defined as a macromolecular
homopolymer derived from a single reactive entity (e.g. monomer) or
a macromolecular copolymer derived from multiple reactive entities,
or mixtures thereof.
[0028] The term "functional polyester resin" is defined as a
polyester (co)polymer including one or more hydroxyl groups and/or
one or more carboxyl groups.
[0029] The term "dispersed in" with respect to a polymer "dispersed
in" a carrier liquid means that the polymer can be mixed into a
carrier liquid to form a macroscopically uniform, single phase or
multiphase (e.g. solid/liquid) fluid mixture, and is intended to
include solutions and mixtures wherein the carrier liquid solvates,
swells, and completely or partially-solubilizes the dispersed
polymer.
[0030] The term "substantially nonaqueous carrier liquid" is used
to denote a carrier liquid in which water, if present at all,
constitutes less than about 5% w/w of the carrier liquid.
[0031] The term "cross-linker" is used to denote a chemical
compound containing two or more chemical groups capable of
undergoing inter- or intra-molecular chemical reaction.
[0032] The term "easy open" with respect to an end closure refers
to a container end or lid that is partially cut through during
manufacture, leaving intact the interior protective coating, to
facilitate opening of the can by the consumer using a ring-pull or
similar opener. Such containers may be particularly useful for
storage of vacuum-packed foodstuffs.
Exemplary Coating Compositions
[0033] The present invention relates to hardenable coating
compositions and protective coating systems for metal substrates
including a functional polyester resin, a cross-linker, and a
phenol-formaldehyde resin. In presently preferred embodiments, the
functional polyester resin is a mixture of a hydroxyl-functional
polyester resin and a carboxyl-functional polyester resin, and the
cross-linker is a blocked-isocyanate cross-linker containing at
least two blocked isocyanate groups. In more preferred embodiments,
the hardenable coating composition includes one or more of a
resole-formaldehyde resin, a substantially nonaqueous carrier
liquid, a catalyst or a pigment. The hardenable coating
compositions are preferably substantially free of mobile BPA, BPF,
BADGE and BFDGE. More preferably, the coating compositions are
essentially free of mobile BPA, BPF, BADGE and BFDGE. Most
preferably, the coating compositions are completely free of BPA,
BPF, BADGE and BFDGE.
[0034] The coating composition contains at least one functional
polyester resin. A single functional polyester resin or a mixture
of one or more functional polyester resins may be used according to
the present invention. The functional polyester resin or mixture of
resins is typically present in the coating composition in an amount
from about 50% to about 99%, more preferably from about 70% to
about 95%, most preferably from about 75% to about 90% w/w on a
non-volatile solids basis.
[0035] The chemical composition of the functional polyester resin
broadly encompasses polyester resins containing one or more
hydroxyl and/or carboxyl groups. Suitable polyester resins may be
saturated, unsaturated, linear or branched, provided the resin
contains at least one hydroxyl or carboxyl functional group. In
some embodiments, a single functional polyester resin containing at
least one hydroxyl and at least one carboxyl group may be used. In
such embodiments, the polyester resin typically exhibits a hydroxyl
number of from about 5 to about 150 mg KOH per gram of functional
polyester resin on a non-volatile solids basis, and a carboxyl
number of from about 50 to about 250 mg KOH per gram of functional
polyester resin on a non-volatile solids basis.
[0036] In certain presently preferred embodiments, mixtures of a
hydroxyl-functional polyester resin and a carboxyl-functional
polyester resin are used, preferably at a weight ratio of
hydroxyl-functional polyester resin to carboxyl-functional
polyester resin of from about 50 to 1 to about 600 to 1 parts by
weight on a non-volatile solids basis. Preferably, the amount of
carboxyl-functional polyester resin in the coating composition is
from about 0% to about 5% w/w, more preferably from about 0.1% to
about 1.5% w/w, most preferably from about 0.3% to about 0.5% w/w
of the coating composition on a non-volatile solids basis.
[0037] When a mixture of a hydroxyl-functional and a
carboxyl-functional polyester resin is used, the
hydroxyl-functional polyester resin preferably exhibits a hydroxyl
number from about 5 to about 200 mg KOH per gram, more preferably
from about 50 to about 175 mg KOH per gram, most preferably from
about 75 to about 150 mg KOH per gram functional polyester resin on
a non-volatile solids basis. Similarly, the carboxyl-functional
polyester resin is preferably selected to exhibit an acid number
(AN) of about 100 to about 300 mg KOH/g, more preferably from about
150 to about 275 mg KOH/g, most preferably from about 180 to about
250 mg KOH/g functional polyester resin on a non-volatile solids
basis.
[0038] Acid number may be determined using the titrimetric method
described in ISO Standard XP-000892989. Hydroxyl number may be
determined using the same standard test method, substituting a
solution of hydrochloric acid in ethanol for the potassium
hydroxide in ethanol titrant, and expressing the neutralization
endpoint equivalents of hydrochloric acid in terms of the molar
equivalents of potassium hydroxide.
[0039] The preferred functional polyester resins according to the
present invention are typically macromolecules exhibiting a number
average molecular weight from about 500 to about 10,000 Daltons
(Da), more preferably from about 1,000 to about 7,500 Da, most
preferably from about 2,000 to about 5,000 Da. In some embodiments,
the functional polyester resin exhibits a glass transition
temperature (T.sub.g) greater than about 50.degree. C., more
preferably greater than about 60.degree. C. Preferably, the
functional polyester resin exhibits a T.sub.g less than about
100.degree. C., more preferably less than about 90.degree. C.
[0040] Suitable functional polyester resins are typically prepared
by condensation (esterification) according to known processes [see,
for example, Zeno Wicks, Jr., Frank N. Jones and S. Peter Pappas,
Organic Coatings: Science and Technology, Vol. 1, pp. 122-132 (John
Wiley & Sons: New York, 1992)]. The functional polyester resin
is usually derived from a mixture of at least one poly-functional
alcohol (polyol), generally a dihydroxy or trihydroxy alcohol,
esterified with excess equivalents of a mixture of at least one
dicarboxylic acid or anhydride, generally an aromatic dicarboxylic
acid or anhydride.
[0041] The functional polyester resins are typically prepared from
an aromatic or aliphatic polycarboxylic acid or anhydride, and an
aromatic or aliphatic diol, triol, or polyol. The diol,
polycarboxylic acid and/or anhydride are combined in correct
proportions and chemically reacted using standard esterification
(condensation) procedures to provide a polyester having functional
groups at the terminal ends of the polyester resin, preferably
hydroxyl groups. Hydroxyl groups can be positioned at the terminal
end of the polyester by utilizing excess diol, triol, or polyol in
the reaction. A triol or polyol is typically used to provide a
branched, as opposed to linear, polyester.
[0042] Examples of suitable polycarboxylic acids or anhydrides
include, but are not limited to, maleic anhydride, maleic acid,
fumaric acid, succinic anhydride, succinic acid, adipic acid,
phthalic acid, phthalic anhydride, 5-tert-butyl isophthatic acid,
tetrahydrophthalic anhydride, hexahydrophthalic anhydride,
endomethylenetetrahydrophthalic anhydride, azelaic acid, sebacic
acid, tetrachloro-phthalic anhydride, chlorendic acid, isophthalic
acid, trimellitic anhydride, terephthalic acid, a naphthalene
dicarboxylic acid, cyclohexane-dicarboxylic acid, glutaric acid,
and mixtures thereof. It is also understood that an esterifiable
derivative of a polycarboxylic acid, such as a dimethyl ester or
anhydride of a polycarboxylic acid, can be used to prepare the
polyester.
[0043] Customarily, dicarboxylic acids and their esterifiable
derivatives are used, for example phthalic acid, isophthalic acid,
terephthalic acid, 1,4-cyclohexanedicarboxylic acid, succinic acid,
sebacic acid, methyltetrahydrophthalic acid,
methylhexahydrophthalic acid, tetrahydrophthalic acid,
dodecanedioic acid, adipic acid, azelaic acid,
naphthalenedicarboxylic acid, pyromellitic acid and/or dimer fatty
acids, acid anhydrides thereof and/or lower alkyl esters, for
example methyl esters. Tri-carboxylic acids, e.g. trimellitic acid,
may also be used.
[0044] Preferred polycarboxylic acids and their esterifiable
derivatives contain aromatic functionality. Examples of preferred
aromatic dicarboxylic acids are phthalic acid, terephthalic acid,
isophthalic acid and dimer fatty acid; trimellitic acid is a
preferred aromatic tricarboxylic acid. Particularly preferred are
terephthalic and isophthalic acid. The anhydride derivatives of
these acids can also be used if they exist as anhydrides.
[0045] Preferably less than 10% w/w of the dicarboxylic acid
content comprises other aliphatic polyfunctional carboxylic acids.
Examples of other aliphatic polyfunctional carboxylic acids are
malonic acid, succinic acid, glutaric acid, adipic acid, azelaic
acid, suberic acid, sebacic acid, dimer fatty acids, maleic acid
and dimer fatty acids. Hydroxy acids can also be included in the
polyester such as 12-hydroxy stearic acid, lactic acid and
2-hydroxy butanoic acid.
[0046] Examples of suitable diols, trials, and polyols include, but
are not limited to, ethylene glycol, propylene glycol,
1,3-propanediol, glycerol, diethylene glycol, dipropylene glycol,
triethylene glycol, trimethylolpropane, trimethylolethane,
tripropylene glycol, neopentyl glycol, pentaerythritol,
1,4-butanediol, trimethylol propane, hexylene glycol,
cyclohexanedimethanol, a polyethylene or polypropylene glycol
having a weight average molecular weight (M.sub.w) of about 500 Da
or less, isopropylidene bis (p-phenylene-oxypropanol-2), and
mixtures thereof.
[0047] The polyol mixture may include at least one tri-hydroxy
alcohol (e.g. triol), but is predominantly composed of one or more
di-hydroxy alcohol (e.g. glycol or diol). Suitable tri-hydroxy
alcohols include, for example, trimethylolethane,
trimethylopropane, pentaerythritol, dipentaerythritol and glycerol.
Preferred trials are trimethylolethane and trimethylopropane.
Suitable di-hydroxy alcohols include, for example, ethylene glycol,
propylene glycol, 1,2- and/or 1,3-propanediol, diethylene glycol,
dipropylene glycol, triethylene glycol, tetraethylene glycol,
1,4-butanediol, 1,3-butylethylpropanediol,
2-methyl-1,3-propanediol, 1,5-pentanediol, cyclohexanedimethanol,
glycerol, 1,6-hexanediol, neopentyl glycol, pentaerythritol,
trimethylolethane, trimethylolpropane, 1,4-benzyldimethanol and
-ethanol, and 2,4-dimethyl-2-ethylhexane-1,3-diol. Most preferred
are diols include ethylene glycol, propylene glycol, diethylene
glycol, and neopentyl glycol. One skilled in the art understands
that to provide a hydroxyl-terminated polyester, the equivalent
excess of polyol over dicarboxylic acid should generally be
maintained from about 0.02 to about 0.784 on a molar basis, and
preferably from about 0.04 to about 0.554 on a molar basis.
[0048] Similarly, one skilled in the art understands that to
provide a carboxyl-terminated polyester, it is usually preferable
to use a two-step process. First, one prepares a hydroxy-functional
polyester, and then reacts the terminal hydroxyl groups with a
molar excess of dicarboxylic acid. The equivalent excess of
dicarboxylic acid over polyol generally should be maintained from
about 0.02 to about 0.784 on a molar basis, and preferably from
about 0.04 to about 0.554 on a molar basis. A modest amount (e.g.
1-5% w/w) of a tri-functional monomer, e.g. trimellitic anhydride,
may be added to increase the number average carboxyl-functionality
of the polyester resin.
[0049] Various commercially available functional polyester resins
are suitable for use in the present invention. For example,
exemplary URALAC.TM. polyester resins (e.g. URALAC ZW5007SH.TM., a
hydroxyl-functional polyester resin available from DSM Resins U.S.,
Inc., Augusta, Ga.), exemplary Phenodur.TM. polyester resins (e.g.
Phenodur 1150/50EPAC.TM., a carboxyl-functional polyester resin
available from Cytec Surface Specialties, Inc., West Paterson,
N.J.), exemplary VITEL.RTM. polyester resins (e.g. VITEL.RTM.
PE-100 and PE-200 saturated hydroxyl- and carboxyl-functional
polyester resins available from Goodyear Tire & Rubber Co.,
Akron, Ohio), and Dynapol.TM. polyester resins (e.g. Dynapol.TM. L
and LH saturated hydroxyl-functional polyester resins available
from Degussa, Corp., Parsippany, N.J.).
[0050] Coating compositions according to the present invention also
contain a cross-linker, preferably at from about 0.1% to about 10%,
more preferably from about 1% to about 5%, most preferably at from
about 2% to about 4% w/w of the coating composition on a
non-volatile solids basis (i.e. excluding optional solvents or
carrier liquids). The cross-linker preferably contains two or more
functional groups capable of undergoing chemical reaction with one
or more of the hydroxyl-functional polyester resin, the
phenol-formaldehyde resin, the carboxyl-functional polyester resin
and and/or the optional cresol-formaldehyde resin.
[0051] The choice of particular cross-linker typically depends on
the particular product being formulated. For example, some coating
compositions are highly colored (e.g., gold-colored coatings).
These coatings may typically be formulated using cross-linkers that
themselves tend to have a yellowish color. In contrast, white or
clear coatings are generally formulated using non-yellowing
cross-linkers, or only a small amount of a yellowing cross-linker.
Preferred cross-linkers are substantially free of mobile BPA, BPF,
BADGE and BFDGE.
[0052] The cross-linker may be a single molecule, a dimer, an
oligomer, a (co)polymer or a mixture thereof. Preferably, the
cross-linker is a polymeric material, more preferably a
(co)polymer. Any of the well-known class of amino-, hydroxyl- or
isocyanate-functional cross-linkable (co)polymers can be used. For
example, aminoplast and phenoplast (i.e. phenolic) cross-linkable
resins containing two or more active hydrogen (e.g. amino or
hydroxyl) groups may be used. Preferably, blocked isocyanate
cross-linkers containing two or more blocked isocyanate groups, or
an isocyanate group and a vinyl group, can be used in the coating
compositions.
[0053] In certain presently preferred embodiments, the cross-linker
is selected to be a blocked isocyanate having two or more
isocyanate functional groups, or an isocyanate group and a vinyl
group, capable of cross-linking with at least one component of the
coating composition. Preferably, the blocked isocyanate is an
aliphatic and/or cycloaliphatic blocked polyisocyanate, for example
HDI (hexamethylene diisocyanate), IPDI (isophorone diisocyanate),
TMXDI (bis[4-isocyanatocyclohexyl]methane), H.sub.12MDI
(tetramethylene-m-xylidene diisocyanate), TMI
(isopropenyldimethyl-benzylisocyanate) and dimers or trimers
thereof Preferred blocking agents include, for example, n-butanone
oxime, .epsilon.-caprolactam, diethyl malonate, and secondary
amines.
[0054] Suitable blocked isocyanate cross-linkers are commercially
available. Examples of suitable commercially available blocked
isocyanate cross-linkers include VESTANAT.TM. B 1358 A ,
VESTANAT.TM. EP B 1186 A , VESTANAT.TM. EP B 1299 SV (all available
from Degussa Corp., Marl, Germany); and DESMODUR.TM. VPLS 2078 and
DESMODUR.TM. BL 3175 (available from Bayer A.G., Leverkusen,
Germany).
[0055] Cross-linkable aminoplast resins may also be used, for
example the condensation products of aldehydes such as
formaldehyde, acetaldehyde, crotonaldehyde, and benzaldehyde with
amino or amido group-containing substances such as urea, melamine
and benzoguanamine. Examples of suitable aminoplast cross-linkers
include, without limitation, (co)polymers containing two or more
amino functional groups. Suitable aminoplast cross-linkers are
commercially available, and include benzoguanamine-formaldehyde
(co)polymers, melamine-formaldehyde (co)polymers, esterified
melamine-formaldehyde (co)polymers, and urea-formadehyde
(co)polymers. One specific example of a useful aminoplast
cross-linker is the fully alkylated melamine-formaldehyde
(co)polymer commercially available from Cytec Industries (Cytec
Industries GMBH, Neuss, Germany) under the trade name of CYMEL
303.
[0056] Cross-linkable phenoplast resins may also be used, for
example the condensation products of aldehydes with phenols.
Formaldehyde and acetaldehyde are preferred aldehydes. Various
phenols can be employed such as phenol, cresol, p-phenylphenol,
p-tert-butylphenol, p-tert-amylphenol, and cyclopentylphenol.
Examples of suitable cross-linking phenoplast (i.e. phenolic)
resins include (co)polymers containing two or more hydroxyl
functional groups and which are substantially free of mobile BPA,
BPF, BADGE and BFDGE.
[0057] In certain preferred embodiments, phenol-formaldehyde
cross-linkers of the resole type may be used, for example phenol,
butylphenol, xylenol- and cresol-formaldehyde types, the types
specifically etherified with butanol being preferred for protective
container coatings [see, for example, Zeno Wicks, Jr., Frank N.
Jones and S. Peter Pappas, Organic Coatings: Science and
Technology, Vol. 1, pp. 184-186 (John Wiley & Sons: New York,
1992)].
[0058] Suitable phenoplast and aminoplast cross-linkers are
commercially available. Examples of suitable commercially available
phenol-formaldehyde cross-linkable resins include those known by
the tradenames DUREZ.TM. and VARCUM.TM. from DUREZ Corp. (Dallas,
Tex.) or Reichhold Chemical AG (Austria); (CO)POLYMEROX.TM. from
Monsanto Chemical Co. (St. Louis, Mo.); AROFENE.TM. and AROTAP.TM.
from Ashland Chemical Co. (Dublin, Ohio); and BAKELITE.TM. from
Bakelite A.G. (Iserlohn, Germany).
[0059] In addition to the functional polyester resin and the
cross-linker, the coating composition also contains a phenolic
resin, preferably a phenol-formaldehyde resin at from about 0.5% to
about 10%, more preferably from about 1% to about 5% wlw of the
coating composition on a non-volatile solids basis. The choice of
particular phenolic resin typically depends on the particular
product being formulated. For example, some coating compositions
are highly colored (e.g., gold-colored coatings). These coatings
may typically be formulated using phenol-formaldehyde resins that
tend to have a red or yellowish color. In contrast, white or clear
coatings are generally formulated using non-yellowing
resole-formaldehyde resins, or only a small amount of a yellowing
resin. Preferred phenol-formaldehyde resins are substantially free
of mobile BPA, BPF, BADGE and BFDGE.
[0060] Preferably, the phenol-formaldehyde resin is a polymeric
material, more preferably a (co)polymer. Preferably, the
phenol-formaldehyde resin contains at least two hydroxyl groups
capable of undergoing chemical reaction with at least one or more
of the functional polyester resin and/or the cross-linker, thereby
effecting cross-linking within the coating composition upon
curing.
[0061] Suitable phenol-formaldehyde resins are commercially
available. Examples of commercially available phenol-formaldehyde
resins include those known by the tradenames DUREZ.TM. and
VARCUM.TM. from DUREZ Corp. (Dallas, Tex.) or Reichhold Chemical AG
(Austria); (CO)POLYMEROX.TM. from Monsanto Chemical Co. (St. Louis,
Mo.) ; AROFENE.TM. and AROTAP.TM. from Ashland Chemical Co.
(Dublin, Ohio); and BAKELITE.TM. from Bakelite A.G. (Iserlohn,
Germany). A presently preferred commercial phenol-formaldehyde
resin is BAKELITE.TM. PF6520 LB.
[0062] In certain presently preferred embodiments, a
resole-formaldehyde resin not derived from BPA or Novolac
diglycidyl ether (NOGE) may be used in combination with a
phenol-formaldehyde resin to impart improved characteristics to the
cured protective coating composition. While not wishing to be bound
by any particular theory, applicants presently believe that a
phenol-formaldehyde resin may impart improved acid resistance to a
cured protective coating composition, while a resole-formaldehyde
resin may impart improved flexibility to a cured protective coating
composition.
[0063] A presently preferred commercial resole-formaldehyde resin
is BAKELITE.TM. HARZ 9989 LB. More preferably, a combination of
BAKELITE.TM. HARZ 9989 LB and BAKELITE.TM. PF6520 LB is used in the
coating composition, preferably at a weight ratio of from about 1
to 1 to about 4 to 1, more preferably from about 2 to 1 to about 3
to 1 on a weight basis of BAKELITE.TM. HARZ 9989 LB to BAKELITE.TM.
PF6520 LB based on non-volatile solids.
[0064] As noted above, in some presently preferred embodiments, the
phenol-formaldehyde resin is also cross-linkable. In other
exemplary embodiments, the phenol-formaldehyde resin may be used in
conjunction with one or more suitable cross-linkable aminoplast
resins including, for example: benzoguanamine-formaldehyde
(co)polymers, melamine-formaldehyde (co)polymers, esterified
melamine-formaldehyde (co)polymers, and urea-formadehyde
(co)polymers. One example of a suitable cross-linkable aminoplast
resin is CYMEL 303 (Cytec Industries, Neuss, Germany).
Optional Ingredients
[0065] The types of coating compositions that are found to be most
effective in the present invention are those that combine a
functional polyester resin with a cross-linker and a phenolic resin
in the coating composition. A carrier liquid is thus not an
essential ingredient of the coating composition. If an optional
carrier liquid is used, it is typically a substantially nonaqueous
organic solvent or solvent blend in order to effect more rapid
removal of the carrier liquid and effect more rapid curing of the
under-coat composition upon application to the substrate.
[0066] A substantially nonaqueous organic solvent can include a
relatively low amount of water, such as up to about five percent by
total weight of the coating composition, without adversely
affecting the metal corrosion-inhibiting properties of the
over-coat coating composition, either prior to or after curing. The
water can be added to the composition intentionally, or can be
present in the composition inadvertently, such as when water is
present in a particular component included in the coating
composition.
[0067] Substantially nonaqueous organic solvents or organic solvent
blends may be used advantageously as the carrier liquid, for
example, to obtain more favorable coating rheology, to achieve
faster drying or cure times, or to effectively dissolve or solvate
another component of the coating composition (e.g. the functional
polyester resin or the cross-linker). In general, the substantially
nonaqueous carrier liquid is selected to have sufficient volatility
to evaporate essentially entirely from the coating composition
during the curing process, such as during heating at about
175-205.degree. C. for about 8 to about 12 minutes.
[0068] Organic solvents that are particularly useful as optional
carrier liquids include aliphatic hydrocarbons (e.g. mineral
spirits, kerosene, high flashpoint VM&P naptha, and the like);
aromatic hydrocarbons (e.g. benzene, toluene, xylene, solvent
naphtha 100, 150, 200 and the like); alcohols (e.g. ethanol.
n-propanol, isopropanol, n-butanol, iso-butanol and the like);
ketones (e.g. acetone, 2-butanone, cyclohexanone, methyl aryl
ketones, ethyl aryl ketones, methyl isoamyl ketones, and the like);
esters (e.g. ethyl acetate, butyl acetate and the like); glycols
(e.g. butyl glycol), glycol ethers (e.g. methoxypropanol); glycol
ethers (e.g. ethylene glycol monomethyl ether, ethylene glycol
monoethyl ether, ethylene glycol monobutyl ether, propylene glycol
monomethyl ether, and the like); glycol esters (e.g. butyl glycol
acetate, methoxypropyl acetate and the like); and mixtures
thereof.
[0069] The amount of nonaqueous carrier included in the coating
composition is limited primarily by the desired, or necessary,
rheological properties for application of the composition to the
substrate. Usually, a sufficient amount of nonaqueous carrier is
included in the coating composition to provide a composition that
can be processed easily and that can be applied to a metal
substrate easily and uniformly, and that is sufficiently removed
from the coating composition during curing within the desired cure
time.
[0070] Therefore, essentially any substantially nonaqueous carrier
is useful in the present coating composition as long as the
substantially nonaqueous carrier adequately disperses and/or
solubilizes the coating composition components; is inert with
respect to interacting with composition components; does not
adversely affect the stability of the coating composition or the
ability of the corrosion-inhibition coating to inhibit corrosion of
a metal substrate; evaporates quickly, essentially entirely, and
relatively rapidly to provide a cured coating composition that
inhibits the corrosion of a metal substrate, demonstrates good
adhesion and flexibility, and has good chemical and physical
properties.
[0071] One optional ingredient is a catalyst to increase the rate
of cure or cross-linking in the coating compositions. Generally,
acid catalysts may be used to accelerate the rate of cure of the
coating compositions. The catalyst is typically present in an
amount of 0.05% to about 5%, and preferably about 0.1% to about
1.5%, by weight of nonvolatile material.
[0072] Examples of suitable catalysts, include, but are not limited
to, quaternary ammonium compounds, phosphorous compounds, and tin
and zinc compounds, like a tetraalkyl ammonium halide, a tetraalkyl
or tetraaryl phosphonium iodide or acetate, tin octoate, zinc
octoate, triphenylphosphine, and similar catalysts known to persons
skilled in the art.
[0073] Catalysts that may be suitable for accelerating the rate of
cure of the coating composition include, for example, phosphoric
acid solutions (e.g. an 85% aqueous phosphoric acid solution in
butyl glycol at a 1:1 weight ratio), phosphoric acid ester
solutions (e.g. ADDITOL XK 406.TM., available from Cytec Surface
Specialties, Inc., West Paterson, N.J.), dodecylbenzene sulfonic
acid (e.g. CYCAT 600.TM. available from Cytec Surface Specialties,
Inc., West Paterson, N.J.), and aluminum catalysts (e.g. aluminum
sec-butoxide, AKZO-Nobel Chemicals, Inc., Chicago, Ill.).
[0074] In certain presently preferred embodiments, tin catalysts
are used for accelerating the rate of cure of the coating
composition, preferably a mixture of mono- and di-octyl
tin-mercaptides (e.g. TINSTAB OTS 17 MS.TM. available from
AKZO-Nobel Chemicals, Inc., Chicago, Ill.), or dibutyltin dilaurate
(e.g. FASCAT.TM. available from Atofina Chemicals, Inc.,
Philadelphia, Pa.). One presently preferred catalyst is RD4169
(Tegocoat 722.TM., available from Goldschmidt TIB GmBH, Mannheim,
Germany @20% w/w in Aromatic Solvent 100).
[0075] Coating compositions that are to be used as protective
coatings for metal substrates optionally include a natural or
synthetic lubricant. Suitable lubricants include, for example,
long-chain aliphatic waxes, carnuba waxes, natural and synthetic
wax dispersions (e.g. Lanco Glidd 4518V available from Lubrizol,
Corp., Wickliffe, Ohio), poly(tetrafluoroethylene) waxes, and
mixtures, blends or dispersions thereof. Preferred lubricants
include Luba-Print 887/C Wax Dispersion (a camuba wax dispersion
available from L. P. Bader & Co., GmbH, Rottweil, Germany) and
L16832 (a partially hydrated frying oil derived from sunflower
seeds @20% w/w in Solvent Naptha 150.TM. available from Unilever,
Corp., Austria).
[0076] In some embodiments, a pigment can be added to the coating
compositions. Suitable pigments, such as aluminum flake, titanium
dioxide and zinc oxide, may be added to improve the appearance of
the protective coating, or to act as scavengers for hydrogen
sulfide emitted by foodstuffs that acts to stain or darken the
protective coating. A pigment like aluminum flake can be present in
the coating compositions, typically at a concentration from about
two to about 15 percent by weight, more typically from about five
to about 10 percent by weight of the composition on a non-volatile
solids basis. A pigment like titanium dioxide can also be present
in the coating compositions, typically in an amount from about 35%
to about 50% by weight, more typically from about 40 to about 45
percent by weight of the coating composition on a non-volatile
solids basis. Zinc oxide can also be present in the coating
compositions, typically in an amount from about 0.5% to about 30%
by weight, more typically from about five to about 15 percent by
weight of the coating composition on a non-volatile solids
basis.
[0077] In some embodiments, one or more additional (co)polymer
components may be added to the coating compositions. Suitable
(co)polymers include solution vinyl (PVC) (co)polymers, solution
poly(vinyl)butyral (co)polymers, dispersed or solution
meth(acrylic) copolymers, and solution polyester resins. Suitable
polymers are commercially available, and include UCAR.TM. solution
vinyl (co)polymers (available from Dow Chemical Co., Midland
Mich.), BUTVAR.TM. solution poly(vinyl)butyral (co)polymers
(available from Solutia, Inc., Philadelphia, Pa.), ELVACITE
solution (meth)acrylic (co)polymers, and VITEL.TM. solution
polyester resins.
[0078] Depending upon the desired application, the coating
compositions may include other additives such as water, coalescing
solvents, leveling agents, surfactants, wetting agents, dispersants
(e.g. lecithin), defoamers (e.g. modified (poly)siloxanes),
thickening agents (e.g. methyl cellulose), cure accelerators,
suspending agents, adhesion promoters, cross-linking agents,
corrosion inhibitors, fillers (e.g. titanium dioxide, zinc oxide,
aluminum), matting agents (e.g. precipitated silica) and the like.
Presently preferred additives include BYK-357 (available from
BYK-Chemie, GmBH, Wesel, Germany) and POLYSLIP VS 86 (available
from Rohm & Haas Corp., Philadelphia, Pa.).
[0079] available from Dow Chemical Co., Midland, Mich.).
Production and Use of the Exemplary Coating Compositions
[0080] The present invention also provides a method of coating a
metal substrate with hardenable coating compositions including a
functional polyester resin, a cross-linker, and a
phenol-formaldehyde resin. In certain presently preferred
embodiments, the hardenable coating compositions include a
functional polyester resin and a blocked isocyanate cross-linker.
In certain more preferred embodiments, the hardenable coating
compositions include a hydroxyl-functional polyester resin, a
carboxyl-functional polyester resin, a blocked isocyanate
cross-linker, and optionally, a cresol-formaldehyde resin, a
substantially nonaqueous carrier liquid, a catalyst and a
pigment.
[0081] In presently preferred embodiments, a method of coating a
metal substrate to provide a composite material is provided wherein
the composite material is completely free of BPA, BPF, BADGE and
BFDGE. In certain preferred embodiments, the coating composition is
substantially free of mobile BPA, BPF, BADGE and BFDGE. The
composite material is particularly useful in fabricating metal
foodstuffs storage containers, including multi-part containers
having "easy-open" end closures, wherein the hardened protective
coating contacts the foodstuffs.
[0082] Further provided is a metal foodstuffs storage container
derived from a metal substrate having at least one surface
substantially coated with the hardened coating composition that is
substantially free of mobile BPA, BPF, BADGE and BFDGE. Exemplary
metal substrate protective coating compositions of the present
invention may be used as protective surface coatings in fabricating
metal packages of tinplate, electrolytic tinplate, aluminum and tin
free steel. Exemplary coating systems may be used for both the
interior and exterior coating of three-piece and deep-drawn metal
foodstuff containers, but are particularly preferred for interior
coating of foodstuff containers and "easy open" end closures,
wherein the hardened protective coating contacts the foodstuff.
[0083] The coating compositions of the present invention may be
prepared by conventional methods in various ways. For example, the
coating compositions may be prepared by simply admixing the
functional polyester resin, the cross-linker, the
phenol-formaldehyde resin, and any optional ingredients, in any
desired order, with sufficient agitation. The resulting mixture may
be admixed until all the composition ingredients are substantially
homogeneously blended.
[0084] Alternatively, the coating compositions may be prepared as a
liquid solution or dispersion by admixing to an optional
substantially nonaqueous carrier liquid the functional polyester
resin, the cross-linker, the phenol-formaldehyde resin, and any
optional ingredients, in any desired order, with sufficient
agitation. An additional amount of a substantially nonaqueous
carrier liquid may be added to the coating compositions to adjust
the amount of nonvolatile material in the coating composition to a
desirable level for effective coating. For example, the coating
composition may be prepared by adding the phenolic(co)polymer
material to a solution of the polyester resin in a solvent mixture
that may include a ketone, an ester, aromatic solvents and a small
amount of water.
[0085] Where, as preferred, the coating composition is applied as a
liquid coating, the coating composition is typically produced by
intensive mixing of the raw materials at temperatures of from about
10.degree. C. to about 40.degree. C., more preferably from about
15.degree. C. to about 35.degree. C., to obtain a substantially
homogenous liquid. When applied as a liquid coating, the coating
composition typically exhibits a solids content from about 20% to
about 70% by weight nonvolatile material, more preferably from
about 25% to about 50% by weight nonvolatile material.
[0086] The coating composition is preferably applied as a
dispersion of solids in a substantially nonaqueous carrier liquid,
and preferably exhibits a solids content from about 5% to about
70%, more preferably from about 15% to about 65% by weight, most
preferably from about 25% to about 50% by weight nonvolatile
material.
[0087] If the coating compositions are prepared with optional
particulate components, such as a pigment, the steps of preparation
may be varied accordingly. In particular, the coating composition
may preferably be produced by intensive mixing or media-milling of
the raw materials at temperatures of from about 10.degree. C. to
about 40.degree. C., more preferably from about 15.degree. C. to
about 35.degree. C., to obtain a substantially homogenous
solid/liquid dispersion. In embodiments of the present invention
that incorporate pigments, such as aluminum flake, zinc oxide and
titanium dioxide, the resulting pigmented coating composition
typically has a pigment-to-binder ratio of about 0.5:1 to about
0.85:1, and more typically about 0.6:1 to about 0.7:1.
Pigment-to-binder ratio is a measure, on the basis of weight, of
parts of pigment for every 1 part of (co)polymer, or non-pigment,
which includes all coating components that are not pigment and not
volatilized after the curing step.
[0088] The hardenable coating compositions of the present invention
are useful as protective coatings to prevent contamination of
foodstuffs contained in a metal packaging container by the
packaging metal or the protective lacquer, and to prevent attack by
the foodstuffs on the metal container. The inventive protective
coating compositions are particularly effective at imparting
resistance to attack by acidic foodstuffs and beverages. The
compositions are especially useful in coating food or beverage
cans, particularly the interiors of such cans. Their virtually
undetectable levels of BPA, BPF, BADGE and BFDGE and their other
chemical, physical and mechanical properties make them particularly
desirable compositions for coating the interior of multi-part
foodstuffs storage containers.
[0089] The aforementioned coating compositions are particularly
well adapted for use as an internal surface coating for multi-part
foodstuffs packaging containers (e.g., two-piece cans, three-piece
cans, etc.). Two-piece cans are manufactured by joining a can body
(typically a drawn metal body) with a can end closure (typically a
drawn metal end). The inventive coating compositions are well
suited for use in food contact situations and may be used on the
inside of such cans and components used in fabricating foodstuffs
containers. The coating systems of the present invention are
particularly well suited for providing a protective coating to the
interior surface of "easy-open" end closures used in fabricating
containers for foodstuffs and beverages, particularly for
vacuum-packed foodstuffs.
[0090] Protective coatings for fabricating food and beverage
containers may be applied to metal substrates and cured into films
at high speed, on high-speed coating lines (e.g., coil coating
lines). The coating agents are applied in the roller coating
process either continuously on coil lines or batch-wise on sheet
coating lines to thin metals such as aluminum, tinplate, tin free
steel or chromed steel, and then reacted at high temperatures. The
coated metals thus produced are then shaped to form the desired
metal packaging articles by processes such as, for example,
deep-drawing, stamping, creasing and flanging. This machining
requires very high flexibility and excellent adhesion of the
coating agents used. The protective coatings thus should preferably
not experience any change in protective function due to the
reshaping processes and should preferably exhibit good substrate
adhesion and intact film surfaces after processing into
containers.
[0091] Modem high-speed coil coating lines require coatings that
will dry and cure within a few seconds when heated rapidly to peak
metal temperatures of 420.degree. F. to 550.degree. F. (about
215.degree. C. to about 300.degree. C.). Many metal packaging
articles, after filling with the foods, are subjected to exposure
to similar high temperature in thermal processes for food
preservation (e.g. pasteurization or sterilization). After these
high temperature thermal processes, the protective coatings ideally
exhibit little or no change with respect to protective function,
adhesion, flexibility, appearance, or chemical composition.
[0092] The inventive coating compositions may generally be applied
as coatings to a variety of metal substrates such as tinplate, tin
free steel, aluminum and its alloys, and the like. The compositions
may be applied as a film by conventional means such as brushing,
roller coating or spraying. Roller coating is the preferred method
when coating flat metal coils or sheets for can manufacture, and
spraying is typically preferred when coating preformed cans.
[0093] Preferably, the coating compositions are applied as a
substantially uniform and continuous defect-free layer or film
directly on the metallic substrate, although in some embodiments, a
primer layer may be applied to the metal substrate before
application of the coating compositions according to the present
invention. Preferably, the cured coating compositions are
substantially free from surface defects, such as, for example,
craters, pinholes, and de-wet regions.
[0094] Metal coatings are generally applied to metal sheets in one
of two ways, each of which involves different coating and curing
conditions. The coated metal sheets may be fabricated into can
bodies or ends in a later stage of the manufacturing operation. One
process, called the sheet bake process, involves roll coating large
metal sheets. These sheets are then placed upright in racks and the
racks are typically placed in ovens for about 10 minutes to achieve
peak metal temperatures of about 180.degree. C. to about
205.degree. C. In a second process known as coil coating, large
rolls of thin gage metal (e.g., steel or aluminum) are unwound,
roll coated, heat cured and rewound. During the coil coating
process, the total residence time in the curing ovens will vary
from about 2 seconds to about 20 seconds with peak metal
temperatures typically reaching about 215.degree. C. to about
300.degree. C.
[0095] The present invention may be useful as a spray applied,
liquid coating for the interior of two-piece drawn and ironed
tinplate food cans (i.e. "tinplate D&I cans"). The present
invention also offers utility in other metal substrate coating
applications. These additional applications include, but are not
limited to: coil coating, sheet coating, and the like.
[0096] A coil coating is described as the coating of a continuous
coil or scroll composed of a metal (e.g., steel or aluminum). Once
coated, the coating coil is subjected to a short thermal, and/or
ultraviolet and/or electromagnetic curing cycle, which lead to the
drying and curing of the coating. Coil coatings provide coated
metal (e.g., steel and/or aluminum) substrates that can be
fabricated into formed articles such as 2-piece drawn food cans,
3-piece food cans, food can ends, drawn and ironed cans, beverage
can ends and the like.
[0097] A sheet coating is described as the coating of separate
pieces of a variety of materials (e.g., steel or aluminum) that
have been pre-cut into square or rectangular `sheets`. Typical
dimensions of these sheets are approximately one square meter. Once
coated, each sheet is cured. Once dried and cured, the sheets of
the coated substrate are collected and prepared for subsequent
fabrication. Coil coatings provide coated metal (e.g., steel or
aluminum) substrate that can be successfully fabricated into formed
articles such as 2-piece drawn food cans, 3-piece food cans, food
can ends, drawn and ironed cans, beverage can ends and the
like.
[0098] The method of the present invention includes applying a
first hardenable coating composition to at least one surface of a
metal substrate; applying a second hardenable coating composition
over the first hardenable coating composition, wherein the second
hardenable coating composition includes a hydroxyl-functional
polyester resin, a carboxyl-functional polyester resin, a
cross-linker, and a phenol-formaldehyde resin; and curing the first
and second hardenable coating compositions to provide a hardened
composite coating on the metal substrate.
[0099] One skilled in the art understands that the first and second
hardenable coating compositions may be applied in a single pass, in
multiple passes, or in combination with additional coating layers
placed between the metal substrate and the first hardenable coating
composition (e.g. a primer), or on top of the second coating layer
(e.g. a size coat or lacquer). In some presently preferred
embodiments, the coating compositions of the present invention are
applied in two or more sequential passes to form a multi-layer
composite coating. In exemplary embodiments, the first hardenable
coating composition has a chemical composition that is chemically
distinct from the second hardenable coating. In certain presently
preferred embodiments, the first hardenable coating composition has
a chemical composition that is substantially identical to the
chemical composition of the second hardenable coating
composition.
[0100] One skilled in the art further understands that
"substantially identical" coating compositions may have minor
variations in chemical composition with respect to the chemical
nature and concentration of optional ingredients such as solvents,
catalysts, pigments, and the like; and in the overall percent
non-volatile material in the coating compositions. However, the
independently claimed constituents of each hardenable coating
composition (e.g. the hydroxyl-functional and carboxyl-functional
polyester resins, the cross-linker and the phenol-formaldehyde
resin) are preferably present at the same relative weight ratio on
a non-volatile solids basis in "substantially identical" coating
compositions.
[0101] In other presently preferred embodiments, each of the first
and second hardenable coating compositions preferably exhibits a
dry coating weight of from about 6 to about 12 grams per square
meter (g/m.sup.2) on a non-volatile solids basis. The preferred
method of applying the first and second hardenable coating
compositions to the metal substrate is roll coating, for example,
by direct roll coating, reverse roll coating, rotogravure coating,
and the like. The present coating compositions can generally be
roll coated to produce cured composite films having overall dry
coating weights of from about 12 g/m.sup.2 to about 24
g/m.sup.2.
[0102] In certain presently preferred embodiments, the first and
second hardenable coating compositions on the surface of the metal
substrate are at least partially cured (i.e. hardened or
cross-linked) by exposure to heat, actinic radiation (e.g.
ultraviolet or infrared curing), electromagnetic radiation (e.g.
electron beam curing), combinations thereof and the like. In
certain most preferred embodiments, the first hardenable coating
composition on the surface of the metal substrate is at least
partially cured before applying the second hardenable coating
composition over the first hardenable coating composition and
curing the composite layers to produce a hardened composite coating
on the metal substrate.
[0103] In various exemplary embodiments, each of or preferably both
of the applied first and second hardenable coating compositions can
be dried and cured by heating to drive off at least a portion of
any optional carrier liquids and to accelerate the cross-linking
reaction of the cross-linker with one or more of the components of
the coating compositions. The coated compositions are typically
heated to about 150-220.degree. C. for about 1 to 20 minutes in
order to form a hardened and dried film. If the coating is applied
using a sheet-bake process, the coated metal substrate is
preferably cured at a temperature of about 175.degree. C. to about
205.degree. C. for about 8 to about 10 minutes. In contrast, when
the coating is carried out using a coil-coating process, the coated
metal substrate is preferably cured by heating for about two to
about 20 seconds at a temperature of about 230.degree. C. to about
300.degree. C.
[0104] The hardened protective coating compositions of the present
invention exhibit good adhesion to both the metal substrate and
within the coated composite layers (i.e. inter-coat adhesion). The
hardened composite coating compositions on metal substrates may be
shaped mechanically to form foodstuffs containers or "easy-open"
end closures; for example by deep-drawing, creasing and flanging.
After forming, the metal containers may be filled with a foodstuff,
and then sterilized. The hardened composite coating compositions of
the present invention generally exhibit good flexibility and
chemical resistance, especially in the presence of foodstuffs
containing acetic acid, citric acid and/or lactic acid, usually
without exhibiting loss of adhesion or discoloration.
[0105] The examples that follow are intended to illustrate the
preparation and use of the presently described invention, but are
not intended to be limiting in any way.
Examples
[0106] In the following examples, the inventive coating
compositions were applied to metal substrates, cured, and used to
fabricate foodstuffs storage containers and particularly metal
closures for food or beverage containers. Example 1 illustrates an
exemplary coating composition according to the present invention.
The exemplary first-coat coating composition comprises a
hydroxyl-functional polyester resin, a carboxyl-functional
polyester resin, a cross-linker and at least one
phenol-formaldehyde resin.
[0107] As shown in Table I, the exemplary first-coat coating
composition of Example 1 includes a hydroxyl-functional polyester
resin (URALAC ZW 5007 SH, available from DSM Resins U.S., Inc.,
Augusta, Ga.); a caprolactam blocked IPDI (blocked isocyanate)
cross-linker (DESMODUR VPLS 2078, available from Bayer A.G.,
Leverkusen, Germany); a phenol-formaldehyde resin (BAKELITE PF 6520
LB, available from Bakelite A.G., Iserlohn, Germany); two optional
resole-formaldehyde resins (PHENODUR PR 285/55IB/B, available from
CYTEC Industries, West Paterson, N.J.; and BAKELITE HARZ 9989 LB,
available from Bakelite A.G., Iserlohn, Germany); a
carboxyl-functional polyester resin (PHENODUR.TM. VPM 1150/50EPAC,
available from CYTEC Industries, West Paterson, N.J.); optional
substantially nonaqueous carrier liquids RHODIASOLV RPDE (available
from Rhodia, U.S.A., Cranbury, N.J.), Aromatic 100 European
(available from Exxon-Mobil Chemical Co., Houston, Tex.) and
acetone (available from Dow Oxygenated Solvents, Midland, Mich.);
an optional catalyst (R4169, a 20% w/w mixture of TEGOCOAT.TM. 722,
available from Goldschmidt TIB GMbH, Mannheim, Germany, in Aromatic
100.TM. solvent, available from Exxon-Mobil Chemical Co., Houston,
Tex.); optional lubricants (LUBA-PRINT 887/C, available from L.P.
Bader & Co., GmBH, Rottweil, Germany; and L16832, a 20% w/w
mixture of partially hydrated frying oil derived from sunflower
seeds and available from Unilever.TM. GMbH, Austria, mixed in
Solvent Naptha 150.TM., available from Exxon-Mobil Chemical Co.,
Houston, Tex.); and optional coating additives (BYK 357, available
from BYK-Chemie, GmBH, Wesel, Germany; and POLYSLIP VS 86,
available from Rohm & Haas Corp., Philadelphia, Pa.).
[0108] The first nine raw materials were combined in the order
listed in Table I, then mixed at a temperature below 40.degree. C.
until a fluid, substantially homogenous mixture was obtained. The
final four raw materials were then added with additional mixing,
and the coating compositions were then immediately coated.
[0109] The exemplary coating composition of Example 1 was applied
to electroplated tin plate scrolls as either a single-coat or a
two-coat coating system in which the first-coat and second-coat
were chemically identical compositions. In both the single-coat and
two-coat examples, the first-coat compositions were cured for
approximately 12 minutes at about 200.degree. C., and the
second-coat compositions were cured for approximately ten minutes
at about 190.degree. C. The cured first-coat compositions exhibited
a coating weight of approximately 8 g/m.sup.2, and the cured
second-coat compositions exhibited a coating weight of
approximately 8-12 g/m.sup.2. The resulting composite coated metal
substrates were converted into 73 mm diameter end closures and
metal cans, which were tested according to the cured film
performance methods described below.
TABLE-US-00001 TABLE I Exemplary Cross-linked Polyester Coating
Composition (Example 1) Amount Raw Material (kg) URALAC .TM. ZW
5007 SH 90.00 RHODIASOLVE .TM. RPDE 30.00 AROMATIC 100 EUROPEAN
10.00 DESMODUR .TM. VP LS 2078 10.00 BAKELITE .TM. HARZ 9989 LB
4.45 BAKELITE .TM. PF 6520 LB 2.80 PHENODUR .TM. PR285/55IB/B 2.70
PHENODUR .TM. VPM1150/50EPAC 0.70 BYK .TM. 357 1.35 R4169 Catalyst
0.85 LUBA-PRINT .TM. 887/C Wax Dispersion 1.75 POLYSLIP .TM. VS 86
Lubricant 1.75 L16832 Lubricant 0.75 TOTAL: 157.10 Acetone >100x
VPM 1150 0.446 (Weight % Non-volatile Solids)
[0110] Example 2 illustrates an exemplary two-coat coating
composition according to the present invention. The exemplary
first-coat coating composition of Example 2 comprises one or more
functional polyester resin and one or more phenol-formaldehyde
resin. As shown in Table II, the exemplary first-coat coating
composition includes a saturated polyester resin (URALAC ZW 5363
SN, available from DSM Resins, Zwolle, The Netherlands) mixed in a
mixture of substantially nonaqueous carrier liquids (Dibasic ester
(DBE) and 1-Methoxy-propyl-2 acetate carrier liquids, both
available from Dow Oxygenated Solvents, Midland, Mich.); a
phenol-formaldehyde resin (BAKELITE 9989LB, available from Bakelite
A.G., Iserlohn, Germany), two optional resole-formaldehyde resins
(BAKELITE 6581LB, available from Bakelite A.G., Iserlohn, Germany;
and PHENODUR PR 612, available from CYTEC Industries, West
Paterson, N.J.); an optional substantially nonaqueous carrier
liquid (Butyl glycol acetate, available from Dow Oxygenated
Solvents, Midland, Mich.); optional catalysts (R4149, 10% w/w
BYK.TM. 310, available from BYK-Chemie, GmBH, Wesel, Germany and
mixed in PM acetate (PMA); and 10% w/w CYCAT.TM. 600, available
from CYTEC Industries, West Paterson, N.J., mixed with Solvent PM);
and an optional coating additive (BYK 357, available from
BYK-Chemie, GmBH, Wesel, Germany).
[0111] The exemplary second-coat coating composition of Example 2
comprises one or more functional polyester resin, a blocked
isocyanate cross-linker and one or more phenol-formaldehyde resin.
As shown in Table II, the exemplary second-coat composition
includes a mixture of two functional saturated polyester resins
(DYNAPOL.TM. LH 826-05A, a 55% w/w mixture in a substantially
nonaqueous carrier liquid available; and DYNAPOL.TM. LS 436-12, a
60% w/w mixture in a substantially nonaqueous carrier liquid, both
available from Degussa, GMbH, Frankfurt, Germany); a caprolactam
blocked IPDI (blocked isocyanate) cross-linker (DESMODUR VPLS 2078,
available from Bayer A.G., Leverkusen, Germany); a
phenol-formaldehyde resin (PHENODUR.TM. PR308, a 62% w/w mixture in
a substantially nonaqueous carrier liquid available from CYTEC
Industries, West Paterson, N.J.); optional substantially nonaqueous
carrier liquids (RHODIASOLV.TM. RPDE, available from Rhodia,
U.S.A., Cranbury, N.J.; and Butyl glycol acetate, available from
Dow Oxygenated Solvents, Midland, Mich.); an optional catalyst
(R4165, a mixture of 37.5% w/w METATIN.TM. Kat. S26, available from
Acima, Buchs, Switzerland; 12.5% w/w FASCAT.TM. 4102, available
from CECA ATO, Paris, France; and 50% w/w of a substantially
nonaqueous carrier liquid, Solvesso.TM. 150, available from
Exxon-Mobil Chemical Co., Houston, Tex.); an optional lubricant
(LUBA-PRINT 887/C, available from L.P. Bader & Co., GmBH,
Rottweil, Germany); and optional coating additives (BYK 357,
available from BYK-Chemie, GmBH, Wesel, Germany; ARADUR.TM. 3380-1,
a 35% w/w mixture in PMA available from Huntsmann GMbH, Frankfurt,
Germany; BETAFRIT.TM. 20% w/w in S150, available from Unilever
GMbH, Frankfurt, Germany; and POLYSLIP VS 86, available from Rohm
& Haas Corp., Philadelphia, Pa.).
[0112] The first-coat composition raw materials of Example 2 were
combined in a vessel in the order listed in Table II, then mixed at
a temperature below 40.degree. C. until a fluid, substantially
homogenous first-coat composition mixture was obtained. The
second-coat composition raw materials of Example 2 were combined in
a separate vessel in the order listed in Table II, then mixed at a
temperature below 40.degree. C. until a fluid, substantially
homogenous mixture second-coat composition mixture was
obtained.
[0113] The exemplary first-coat coating composition of Example 2
was applied to electroplated tin plate (ETP) scrolls, and cured at
approximately 200.degree. C. for approximately 12 minutes. The
exemplary second-coat coating composition of Example two was then
applied over the surface of the first-coat composition, and cured
at approximately 200.degree. C. for approximately 12 minutes. The
cured first-coat composition exhibited a coating weight of
approximately 6 g/m.sup.2, and the cured second-coat composition
exhibited a coating weight of approximately 12 g/m.sup.2. The
resulting composite coated metal substrates were converted into 99
mm diameter end closures and metal cans, which were tested
according to the cured film performance methods described
below.
[0114] In addition to the extent of cure of the coatings and their
visual aesthetic appearance when coated on the metal substrates,
other important characteristics of the cured coating compositions
of the present invention typically include: (1) providing a coating
capable of adhering to the metal substrate, (2) providing a coating
that exhibits excellent flexibility, and (3) enhancing corrosion
inhibition of the metal substrate, particularly under sterilization
or pasteurization conditions and when exposed to acidic foodstuff
simulants.
TABLE-US-00002 TABLE II Exemplary Cross-linked Polyester Two-coat
Composition (Example 2) Relative Amount Raw Material (% w/w)
First-coat Composition -- URALAC .TM. ZW 5007 SH 72.072 Dibasic
ester 3.917 1-Methoxy-propyl-2-acetate 3.917 BAKELITE .TM. HARZ
9989 LB 6.737 BAKELITE .TM. 6581LB 4.622 PHENODUR .TM. PR612 2.546
Byk .TM. 357 1.175 Byk .TM. 310 @ 10% w/w in PMA 0.470 CYCAT .TM.
600 @ 20% w/w in PM 0.627 Butyl glycol acetate 3.916 Second-coat
Composition -- DYNAPOL .TM. LH 826-05A 57.754 DYNAPOL .TM. LS
436-12 5.348 RHODIASOLVE .TM. RPDE 8.556 BYK .TM. 357 0.428
DESMODUR .TM. VP LS 2078 10.267 ARADUR .TM. 3380-1 (35% w/w in PMA)
2.139 R4165 Catalyst 0.250 LUBA-PRINT .TM. 887/C Wax Dispersion
0.980 POLYSLIP .TM. VS 86 Lubricant 0.980 L16832 (Betafrit .TM. 20%
w/w in S150) 0.606 PHENODUR .TM. PR308 1.996 Butyl glycol acetate
10.695
[0115] Accordingly, the cured composite coatings of Examples 1 and
2 were tested for adhesion to the metal substrate, for flexibility,
for ability to inhibit corrosion of the metal substrate and for
chemical resistance to model foodstuffs and sterilization
conditions. The following test methods are offered to aid in
understanding of the present invention and are not to be construed
as limiting the scope thereof. The coated composite metal
substrates, "easy-open" end closures and multi-part food containers
prepared in Examples 1 and 2 were evaluated according to one or
more of the following cured film performance tests.
[0116] The coating uniformity porosity test method determines the
amount of metal substrate surface that has not been effectively
coated by the protective coating before sterilization. The extent
of metal exposure for metal substrates (e.g. cans or ends) was
determined using a WACO enamel rater (Wilkens-Anderson Co.,
Chicago, Ill.) in 4-second mode using an electrolyte solution
consisting of 989.7 grams deionized water, 10 g sodium chloride
(NaCl) and 0.3 g Aerosol OT-B (available from CYTEC Industries,
West Paterson, N.J.).
[0117] If any uncoated metal is present on the surface of the metal
substrate, then a current is passed between these two probes and
registers as a value on an LED display. The LED displays the
conveyed currents in milliamps, or more commonly referred to as
`mAs`. The current that is passed is directly proportional to the
amount of metal that has not been effectively covered with coating.
The goal is to achieve 100% coating coverage on the metal
substrate, which would result in an LED reading of 0.0 mAs.
[0118] To assess adhesion, cans and can end closures were subjected
to a variety of tests to determine the adhesion of the coating to
the metal substrate, including, for example, the cross hatch
adhesion (CHA) test. Cross-hatch adhesion tests were performed
generally according to AS.TM. Test Method D 3359--Test Method B.
The adhesion rating scale for Example 1 is "A-E", with `A` meaning
that 100% of the coating in this area has maintained adhesion, and
"E" meaning that 100% of the coating has been removed from the
tested area, and so on.
[0119] To evaluate corrosion resistance of the cured films, can
ends were sterilized in 1% w/w NaCl in deionized water, 2% w/w
lactic acid in deionized water, and 3% w/w acetic acid in deionized
water, for about 60 minutes at 131.degree. C. and 15 pounds per
square inch (about 1 atmosphere) pressure, after which porosity was
determined according to the above method.
[0120] In addition, cans were filled with various food simulants
and sterilized for about 60 minutes at 128.degree. C. and 15 pounds
per square inch (about I atmosphere) pressure. These food simulants
included: [0121] 2% w/w NaCl in tap water; [0122] 2% w/w
NaCl/acetic acid in deionized water [0123] 1% w/w Lactic acid in
deionized water [0124] 3% w/w Acetic acid in deionized water [0125]
"R" (2% w/w citric acid and 0.5% Ascorbic acid in deionized water);
[0126] Cysteine Hydrochloride
[0127] After sterilization, the visual appearance of the protective
coatings was assessed with respect to changes from the initial
observation ("unchanged" denotes no change from the initial
observation, i.O) with respect to the appearance of surface
roughness (roughening of the otherwise smooth surface of the
protective coating), blushing (spot-wise discoloration of the
surface of the protective coating), and the appearance of
sulfo-staining (darkening of the surface of the protective coating)
when exposed to cysteine hydrochloride. The visual rating scale for
each parameter is qualitative and is defined as follows: None: No
visual occurence; Slight: slight visual occurence; Moderate:
Frequent visual occurrence; and Heavy: heavy visual occurence.
Cross-hatch adhesion (CHA) was also determined on the sterilized
protective coatings.
[0128] As shown in Table III, the inventive BPA, BPF, BADGE and
BFDGE-free coating composition of Example 1, when applied to a
metal substrate as a single-pass or two-pass protective coating
(i.e. wherein the first-coat composition has a chemical composition
substantially identical to the chemical composition of the
second-coat composition) and converted to an "easy-open" end
closure; exhibited good adhesion, low porosity, and excellent
corrosion resistance even after sterilization under highly acidic
conditions.
[0129] As shown in Table IV, the inventive BPA, BPF, BADGE and
BFDGE-free coating composition of Example 2, when applied to a
metal substrate as a two-coat protective coating (i.e. wherein the
first-coat composition is chemically distinct from the second-coat
composition) and converted to an "easy-open" end closure; also
exhibited good adhesion, low porosity, and excellent corrosion
resistance even after sterilization under acidic conditions.
TABLE-US-00003 TABLE III Performance of Exemplary Single-pass and
Two-pass Cross-linked Polyester Coatings 73 mm End Closures:
Porosity (mA) Example 1 Before Sterilization: 0.2 After
Sterilization 0.4 3% Acetic Acid for 1 hour @ 131.degree. C.
Appearance: Slightly rough Single-pass: -- Porosity (mA) After
Sterilization 1 hour @ 128.degree. C. 2% NaCl/Deionized Water (CHA)
A Appearance: Unchanged 2% NaCl/3% Acetic Acid (CHA) A Appearance:
Unchanged "R" (CHA) A Appearance: Unchanged Cysteine HCl (CHA) A
Appearance: Sulfostaining Two-Pass: -- Porosity (mA) After
Sterilization 1 hour @ 128.degree. C. 2% NaCl/Deionized Water (CHA)
A Appearance: Unchanged 2% NaCl/3% Acetic Acid (CHA) A Appearance:
Unchanged "R" (CHA) A Appearance: Unchanged Cysteine HCl (CHA) A
Appearance: Slight sulfostaining
TABLE-US-00004 TABLE IV Performance of Exemplary Two-coat
Cross-linked Polyester Coating 99 mm ETP End Closures: Porosity
(mA) Example 2 Before Sterilization: 0.6 After Sterilization 1 hour
@ 131.degree. C. -- 1% NaCl/Deionized Water 3.9 2% Lactic
Acid/Deionized Water 2.7 3% Acetic Acid/Deionized Water 9.7
Cross-Hatch Adhesion -- After Sterilization 1 hour @ 128.degree. C.
2% NaCl/Deionized Water (CHA) A Appearance: Unchanged 2% NaCl/3%
Acetic Acid (CHA) A Appearance: Small Blisters on Beading "R" (CHA)
A Appearance: Unchanged Cysteine HCl (CHA) A Appearance:
Blushing
[0130] The above specification, examples and data provide a written
description of the BPA, BPF, BADGE and BADGE-free, hardenable
coating compositions of the present invention, as well as the
methods of making and methods of using the metal substrate coating
system to produce metal foodstuffs storage containers and end
closures according to the present invention. Various preferred
embodiments of the invention were also described. These and other
embodiments of the invention reside within the scope of the
following claims.
* * * * *