WO2000055265A1 - Badge-free can coating - Google Patents

Badge-free can coating Download PDF

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Publication number
WO2000055265A1
WO2000055265A1 PCT/EP2000/001065 EP0001065W WO0055265A1 WO 2000055265 A1 WO2000055265 A1 WO 2000055265A1 EP 0001065 W EP0001065 W EP 0001065W WO 0055265 A1 WO0055265 A1 WO 0055265A1
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WO
WIPO (PCT)
Prior art keywords
coating composition
amount
solvent
coating
lubricant
Prior art date
Application number
PCT/EP2000/001065
Other languages
French (fr)
Inventor
Christian Vogt
Peter Ambrosi
Original Assignee
W.R. Grace & Co.-Conn.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by W.R. Grace & Co.-Conn. filed Critical W.R. Grace & Co.-Conn.
Priority to AU26715/00A priority Critical patent/AU2671500A/en
Priority to EP00905046A priority patent/EP1163305A1/en
Priority to JP2000605687A priority patent/JP2002539319A/en
Priority to CA002363482A priority patent/CA2363482A1/en
Publication of WO2000055265A1 publication Critical patent/WO2000055265A1/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D161/00Coating compositions based on condensation polymers of aldehydes or ketones; Coating compositions based on derivatives of such polymers
    • C09D161/04Condensation polymers of aldehydes or ketones with phenols only
    • C09D161/06Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D167/00Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L27/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
    • C08L27/02Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L27/12Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
    • C08L27/18Homopolymers or copolymers or tetrafluoroethene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L91/00Compositions of oils, fats or waxes; Compositions of derivatives thereof

Definitions

  • Metal containers for receiving foods and beverages generally have one or more coatings to prevent contact between the filled product and metal. This is to prevent or minimize corrosion to the metal by the product and any disadvantageous influences on the quality of the product.
  • coatings are required which are extremely flexible and have a low order of toxicity.
  • Epoxy phenolic type coatings have been applied as lacquers onto metal can stock (e.g., for three-piece cans) and baked to provide coatings having good resistance to aggressive filled products, mechanical performance and metal adhesion.
  • many of these incorporate 2,2'-bis(4- hydroxyphenyl) propane-bis(2,3-epoxypropyl)-ether (or homologues thereof), otherwise known as bisphenol-A-diglycidyl-ether or "BADGE" (Bisphenol- A-DiGlycidyl-Ether).
  • BADGE Bisphenol- A-DiGlycidyl-Ether
  • polyester type coatings such as those cross-linked with amino-type or isocyanate-type resins, are used on the exterior of three-piece cans, but do not resist processing when in contact with food, or do not comply with food laws, and therefore do not yet provide an alternative coating formulation.
  • a novel can coating is need which is substantially BADGE-free (and PVC-free as well).
  • the present invention provides a coating for metal sheet substrates, such as metal cans or metal can stock, which is substantially B ADGE-free. Another objective of the present invention to provide a coating which is substantially free of polyvinyl chloride (PNC).
  • PNC polyvinyl chloride
  • a further objective of the invention is to provide metal can coatings that have suitable flexibility and are safe when processed in contact with food.
  • the coatings should be suitable for three-piece cans as well as deep-drawn metal cans.
  • An exemplary coating of the invention comprises (a) a polyester resin (20-50% wt); (b) a resol resin (1-15% wt.); and (c) a solvent component (35- 79% wt.), all weight percentages based on total coating weight, the coating being substantially free of bisphenol-A-diglycidyl-ether and bisphenol-F- diglycidyl ether (e.g., "BADGE” or "BADGE-type” components), and preferably also substantially free of polyvinyl chloride.
  • the coating comprises a lubricant (0.1-2% wt.) and acid catalyst (0-2% wt).
  • exemplary coating compositions of the invention comprise: (a) a polyester resin in the amount of 20-50% wt.; (b) a resol resin in the amount of 1-15% wt. and comprising a condensation product made from a phenol or homologue thereof and formaldehyde; and (c) a solvent in the amount of 35-79% wt., all weight percentages being based on the total weight of said coating, the coating compositions being substantially free of bisphenol-A-diglycidyl-ether (“BADGE”) and bisphenol-F-diglycidyl ether (a "BADGE-type" component).
  • BADGE bisphenol-A-diglycidyl-ether
  • BADGE-type bisphenol-F-diglycidyl ether
  • the phrase "substantially free” as used within the context of this application means that the coating compositions of the invention have no BADGE, BADGE-type component, or PVC, or at least no more than a de minimus amount of these components, e.g., less than 0.001% by total wt..
  • An exemplary polyester resin component of the invention comprises (a) trimethylolpropane in the amount of 0.1-10% wt. and more preferably 1- 7% wt.; neopentylglycol in the amount of 15-30% wt. and more preferably 20- 25% by wt.; at least one other polyol (e.g., ethylene glycol, propylene glycol) in the amount of 5-20% wt. and more preferably 10-15% wt.; phthalic acid (including iso- and tere-) in the amount of 20-60% wt. and more preferably 20- 25% wt.; and adipic acid in the amount of 10-35% wt. and more preferably 15- 20% wt.
  • a commercially available polyester resin, available from DSM Resins of Zwolle, The Netherlands under the tradename URALAC XP 8481 SN, is believed to be suitable for use as polyester resin component (a) in the present invention.
  • Resol resin component (b) may be characterized as a condensation resin made from a phenol or phenolic homologue (phenol, butyl phenol, cresol, xylenol, Bisphenol A) and formaldehyde.
  • the resol resin comprises Bisphenol A, butyl phenol, xylenol, or a mixture thereof, and formaldehyde.
  • Commercially available resol resins believed to be suitable for use in the present invention are available from Vianova Resins, Germany, under the tradename PriENODUR PR 401 and from Deutsche Shell Chemie, Germany, under the tradename EPICURE DX 200.
  • the resins can be solvated in a solvent or solvent mixture, for example, n-butanol and/ or butylcellusolve, or other conventional solvents used for can coatings.
  • the resin can be etherified with an alcohol (e.g., butanol) and solvated in the solvent or solvent mixture.
  • aromatic hydrocarbons e.g., aromatic 100 or aromatic 150
  • glycolether/glycolether acetate e-g-/ methoxypropanol butylcellusolveacetate, methoxypropylacetate
  • alcohols e.g., isobutanol, diacetone alkohol
  • ketons e.g., methylisobutylketon, is
  • the coating composition further comprises a lubricant which is in a solid form dispersed in solvent.
  • the lubricant may be present in the coating composition in the amount of 0.1-2% wt., and more preferably 0.1- 1% wt.
  • Exemplary lubricants may comprise polyethylene (PE), polypropylene (PP), PTFE, lanoline, carnauba wax and petrolatum.
  • the lubricant comprises PE, PP or PTFE or a mixture of these.
  • Preferred coating compositions also comprise at least one catalyst, preferably an acidic catalyst, such as sulfonic acid (e.g., paratoluene sulfonic acid and dodecyl benzenesulfonic acid), phosphoric acid and phosporic acid ester (e.g., phosphoric acid monobutyl ester), in the amount of 0.05-2.0% wt., and more preferably in the amount of 0.05-1.0% wt.
  • an acidic catalyst such as sulfonic acid (e.g., paratoluene sulfonic acid and dodecyl benzenesulfonic acid), phosphoric acid and phosporic acid ester (e.g., phosphoric acid monobutyl ester)
  • a preferred coating composition of the invention comprises polyester resin (solid) (20-50% wt); resol resin (solid) (1-15% wt); a lubricant (solid) (0.1-2% wt); an acidic catalyst (0-2% wt); and a solvent (35- 79% wt), all percentages based on the total weight of the coating composition.
  • the coating may be applied to a metal substrate or metal plate for a can, such as by roller coating or spray coating, or it may be applied by these means to a formed can. Preferred application is by roller coating to the flat metal before formation of the can.
  • Preferred coating layer weights are 2-15 gsm (grams/ square meter), and more preferably 3-8 gsm. After application, the coating should be cured at 180°C - 210°C, and more preferably at 190°C - 205°C for 6 to 20 minutes, and more preferably 8-13 minutes.
  • Example 1 Example 1
  • An exemplary can coating composition of the invention may be prepared and applied as follows.
  • a coating batch may be formulated as follows, using a blender that can mix the following components into a sufficiently homogeneous composition.
  • the polyester resin comprising trimethylolpropane, neopentylglycol, and other polyols, as previously discussed, is preferably added first into the blender in the amount of 40-85% wt and more preferably 69-80% wt. (based total weight of coating composition).
  • the polyester resin was URALAC XP 8481 SN (from DSM Resins) which was solvated in a solvent mixture that comprised SOLVESSO 150 and butyl cellosolve (which solvents were used in a 4:1 weight ratio).
  • SOLVESSO 150 aromatic hydrocarbon solvent is available from Exxon Chemical, and is believed to have a boiling range of 186-210°C.
  • Butyl cellosolve is otherwise known as butyl glycole (e.g., ethylene glycol mono butyl ether).
  • Exemplary lubricants which are suitable for use in the present invention are PFTE (polytetrafluoroethylene) modified with polyethylene wax, micronised (e.g., specially fine), and are available from Lanco Wax under the designations "TF 1780 EF.” Also available from Lanco Wax is a polyethylene/polypropylene lubricant under the designation "PP 1350 FF" which may also be suitable in the present invention.
  • the lubricant which is in solid form, should be mixed with a suitable solvent or solvents, such as SOLVESSO 100 (an hydrocarbon based solvent from Exxon) and butyl cellosolve, in amounts sufficient to prevent agglomeration of the lubricant in the mixture. Once a homogeneous mixture of the coating components is obtained, this may be roller coated onto steel or alumirtum can stock, for example, and baked at about 200°C for preferably 12-15 minutes. A BADGE-free can coating is thus obtained.
  • SOLVESSO 100 an hydrocarbon based

Abstract

An exemplary coating of the invention, suitable for use as an interior coating for metal cans, comprises (a) a polyester resin; (b) a resol resin; and (c) a solvent, the coating being substantially free of bisphenol-A-diglycidyl-ether and bisphenol-F-diglycidyl ether (e.g., 'BADGE' or 'BADGE-type' components), and preferably also substantially free of polyvinyl chloride.

Description

BADGE-FREE CAN COATING
Background of the Invention
Metal containers for receiving foods and beverages generally have one or more coatings to prevent contact between the filled product and metal. This is to prevent or minimize corrosion to the metal by the product and any disadvantageous influences on the quality of the product. For producing containers of this type, such as steel or tin cans, metal sheets are used which, prior to their shaping (such as for three-piece can production) or deformation (such as for deep drawing process), are coated with suitable coating compositions. In producing cans for foods and beverages, coatings are required which are extremely flexible and have a low order of toxicity.
Epoxy phenolic type coatings have been applied as lacquers onto metal can stock (e.g., for three-piece cans) and baked to provide coatings having good resistance to aggressive filled products, mechanical performance and metal adhesion. However, many of these incorporate 2,2'-bis(4- hydroxyphenyl) propane-bis(2,3-epoxypropyl)-ether (or homologues thereof), otherwise known as bisphenol-A-diglycidyl-ether or "BADGE" (Bisphenol- A-DiGlycidyl-Ether). One objective of the present invention is to provide a novel can coating which is substantially free of BADGE (and BADGE-type components). BADGE-containing formulations do not meet approval in some countries for use in food canning. Currently available polyester type coatings, such as those cross-linked with amino-type or isocyanate-type resins, are used on the exterior of three-piece cans, but do not resist processing when in contact with food, or do not comply with food laws, and therefore do not yet provide an alternative coating formulation. In view of the foregoing disadvantages of the prior art, a novel can coating is need which is substantially BADGE-free (and PVC-free as well).
-l- Summary of the Invention
In surmounting the disadvantages of the prior art, the present invention provides a coating for metal sheet substrates, such as metal cans or metal can stock, which is substantially B ADGE-free. Another objective of the present invention to provide a coating which is substantially free of polyvinyl chloride (PNC).
A further objective of the invention is to provide metal can coatings that have suitable flexibility and are safe when processed in contact with food. The coatings should be suitable for three-piece cans as well as deep-drawn metal cans.
An exemplary coating of the invention comprises (a) a polyester resin (20-50% wt); (b) a resol resin (1-15% wt.); and (c) a solvent component (35- 79% wt.), all weight percentages based on total coating weight, the coating being substantially free of bisphenol-A-diglycidyl-ether and bisphenol-F- diglycidyl ether (e.g., "BADGE" or "BADGE-type" components), and preferably also substantially free of polyvinyl chloride. In further preferred embodiments, the coating comprises a lubricant (0.1-2% wt.) and acid catalyst (0-2% wt).
Further advantages and features of the present invention are discussed hereinafter.
Detailed Description of the Invention
All weight percentages provided herein are based on the total weight of the coating composition including solvent. As summarized above, exemplary coating compositions of the invention comprise: (a) a polyester resin in the amount of 20-50% wt.; (b) a resol resin in the amount of 1-15% wt. and comprising a condensation product made from a phenol or homologue thereof and formaldehyde; and (c) a solvent in the amount of 35-79% wt., all weight percentages being based on the total weight of said coating, the coating compositions being substantially free of bisphenol-A-diglycidyl-ether ("BADGE") and bisphenol-F-diglycidyl ether (a "BADGE-type" component).
The phrase "substantially free" as used within the context of this application means that the coating compositions of the invention have no BADGE, BADGE-type component, or PVC, or at least no more than a de minimus amount of these components, e.g., less than 0.001% by total wt..
An exemplary polyester resin component of the invention comprises (a) trimethylolpropane in the amount of 0.1-10% wt. and more preferably 1- 7% wt.; neopentylglycol in the amount of 15-30% wt. and more preferably 20- 25% by wt.; at least one other polyol (e.g., ethylene glycol, propylene glycol) in the amount of 5-20% wt. and more preferably 10-15% wt.; phthalic acid (including iso- and tere-) in the amount of 20-60% wt. and more preferably 20- 25% wt.; and adipic acid in the amount of 10-35% wt. and more preferably 15- 20% wt. A commercially available polyester resin, available from DSM Resins of Zwolle, The Netherlands under the tradename URALAC XP 8481 SN, is believed to be suitable for use as polyester resin component (a) in the present invention.
Resol resin component (b) may be characterized as a condensation resin made from a phenol or phenolic homologue (phenol, butyl phenol, cresol, xylenol, Bisphenol A) and formaldehyde. Preferably, the resol resin comprises Bisphenol A, butyl phenol, xylenol, or a mixture thereof, and formaldehyde. Commercially available resol resins believed to be suitable for use in the present invention are available from Vianova Resins, Germany, under the tradename PriENODUR PR 401 and from Deutsche Shell Chemie, Germany, under the tradename EPICURE DX 200. The resins can be solvated in a solvent or solvent mixture, for example, n-butanol and/ or butylcellusolve, or other conventional solvents used for can coatings. The resin can be etherified with an alcohol (e.g., butanol) and solvated in the solvent or solvent mixture. Other known solvents that can be used for solvating the polyester and resol resins include aromatic hydrocarbons (e.g., aromatic 100 or aromatic 150), glycolether/glycolether acetate (e-g-/ methoxypropanol butylcellusolveacetate, methoxypropylacetate,), alcohols (e.g., isobutanol, diacetone alkohol), ketons (e.g., methylisobutylketon, isophorone) or esters (e.g., butyl acetate, dibasic esters). In other exemplary coating compositions of the invention, at least two different solvents are used, preferably having different boiling ranges. Preferably, the coating composition further comprises a lubricant which is in a solid form dispersed in solvent. The lubricant may be present in the coating composition in the amount of 0.1-2% wt., and more preferably 0.1- 1% wt. Exemplary lubricants may comprise polyethylene (PE), polypropylene (PP), PTFE, lanoline, carnauba wax and petrolatum. Preferably, the lubricant comprises PE, PP or PTFE or a mixture of these.
Preferred coating compositions also comprise at least one catalyst, preferably an acidic catalyst, such as sulfonic acid (e.g., paratoluene sulfonic acid and dodecyl benzenesulfonic acid), phosphoric acid and phosporic acid ester (e.g., phosphoric acid monobutyl ester), in the amount of 0.05-2.0% wt., and more preferably in the amount of 0.05-1.0% wt.
Accordingly, a preferred coating composition of the invention comprises polyester resin (solid) (20-50% wt); resol resin (solid) (1-15% wt); a lubricant (solid) (0.1-2% wt); an acidic catalyst (0-2% wt); and a solvent (35- 79% wt), all percentages based on the total weight of the coating composition. The coating may be applied to a metal substrate or metal plate for a can, such as by roller coating or spray coating, or it may be applied by these means to a formed can. Preferred application is by roller coating to the flat metal before formation of the can. Preferred coating layer weights are 2-15 gsm (grams/ square meter), and more preferably 3-8 gsm. After application, the coating should be cured at 180°C - 210°C, and more preferably at 190°C - 205°C for 6 to 20 minutes, and more preferably 8-13 minutes. Example 1
An exemplary can coating composition of the invention may be prepared and applied as follows. A coating batch may be formulated as follows, using a blender that can mix the following components into a sufficiently homogeneous composition. The polyester resin, comprising trimethylolpropane, neopentylglycol, and other polyols, as previously discussed, is preferably added first into the blender in the amount of 40-85% wt and more preferably 69-80% wt. (based total weight of coating composition). The polyester resin was URALAC XP 8481 SN (from DSM Resins) which was solvated in a solvent mixture that comprised SOLVESSO 150 and butyl cellosolve (which solvents were used in a 4:1 weight ratio). SOLVESSO 150 aromatic hydrocarbon solvent is available from Exxon Chemical, and is believed to have a boiling range of 186-210°C. Butyl cellosolve is otherwise known as butyl glycole (e.g., ethylene glycol mono butyl ether). Thus, once the polyester resin is introduced into the blender, then the other components can be introduced thereafter during mixing, as follows:
Figure imgf000007_0001
Exemplary lubricants which are suitable for use in the present invention are PFTE (polytetrafluoroethylene) modified with polyethylene wax, micronised (e.g., specially fine), and are available from Lanco Wax under the designations "TF 1780 EF." Also available from Lanco Wax is a polyethylene/polypropylene lubricant under the designation "PP 1350 FF" which may also be suitable in the present invention. The lubricant, which is in solid form, should be mixed with a suitable solvent or solvents, such as SOLVESSO 100 (an hydrocarbon based solvent from Exxon) and butyl cellosolve, in amounts sufficient to prevent agglomeration of the lubricant in the mixture. Once a homogeneous mixture of the coating components is obtained, this may be roller coated onto steel or alumirtum can stock, for example, and baked at about 200°C for preferably 12-15 minutes. A BADGE-free can coating is thus obtained.
The foregoing discussion is provided by way of illustration only and is not intended to limit the scope of the invention as set forth in the claims.

Claims

Claims :
1. A coating composition for metal capable of being formed into a container, said coating composition comprising:
a) a polyester resin in the amount of 20-50% by wt.;
b) a resol resin in the amount of 1-15% by wt. and comprising a condensation product made from a phenol or homolo- gue thereof and formaldehyde; and
c) a solvent component in the amount of 35-79% by wt., all foregoing weight percentages being based on the total weight of the coating composition; and
the coating composition being substantially free of bisphenol-A-diglycidyl ether, bisphenol-F-diglycidyl ether, homo- logues tehreof , and polyvinyl chloride .
2. The coating composition of claim 1 further comprising at least one lubricant.
3. The coating composition of claim 2 wherein said lubricant comprises polyethylene, polypropylene, tetrafluor ethylene or a mixture of these.
4. The coating composition of any claims 1-3 wherein said polyester resin comprises trimethylolpropane in the amount of 0.1-10% by wt., neopentylglycol in the amount of 15-30% by wt., at least one other polyol in the amount of 5-20% by wt., a phthalic acid in the amount of 20-60% by wt., and adipic acid in the amount of 10-35% by wt.
5. The coating composition of any of claims 1-4 wherein said resol resin is a condensation product made from phenol, butyl phenol, cresol, xylenol, bisphenol A, or a mixture thereof .
6. The coating composition of claim 5 wherein said resol resin comprises bisphenol A, butyl phenol, and xylenol or a mixture thereof .
7. The coating composition of any of claims 1-6 wherein said solvent comprises an aromatic hydrocarbon, a glycolether/ glycolether acetate, n-butanol, an aromatic hydrocarbon, a glycoiether/glycolether acetate, an alcohol, an ester, or a mixture thereof .
8. The coating composition of any of claims 1-7 comprising: a polyester resin dispersed in a solvent (20-50% by wt.); a resol resin dissolved in a solvent (1-15% by wt.); a lubricant in solid form dispersed in at least one solvent (0.1-2% by wt.); an acidic catalyst (0-2% by wt . ) ; and said solvent or solvents being operative to solvate said resins and lubricant, all percentages based on the total weight of the coating composition.
9. The coating composition of claim 8 wherein said polyester and said resol resin are combined together using at least two different solvents.
10. The coating composition of any of claims 1-9 wherein said coating is coated onto a metal substrate.
11. The coating composition of claim 1 wherein said polyester resin comprises trimethylolpropane and neopentylglycol; said resol resin comprises a condensation resin made from a phenol or phenolic ho ologue and formaldehyde; at least one lubricant comprising polyethylene, polypropylene, PTFE, lanoline, carnauba wax, petrolatum, or a mixture thereof; and at least two different solvents .
12. The coating composition of claim 11 wherein at least one of said two different solvents comprises an aromatic hydrocarbon type solvent.
13. The coating composition of any of claims 1-12 wherein said conposition comprises at least two different solvent.? having dif erent boiling ranges .
14. A coated metal substrate comprising a metal sheet having the coating composition of any of claims 1-13.
15. A coated can body having the coating composition according to any of claims 1-13.
16. The coating composition of claim 1 further comprising at least one catalyst.
AMENDED CLAIMS
[received by the International Bureau on 12 July 2000 (12.07.00); original claims 1 and 6 replaced by amended claim 1 ; original claim 5 cancelled; remaining claims renumbered accordingly (3 pages)]
1. A coating composition for metal capable of being formed into a container, said coating composition comprising:
a) a polyester resin in the amount of 20-50% by wt.;
b) a resol resin in the amount of 1-15% by wt . and comprising a condensation product made from bisphenol A, butyl phenol, xylenol or a mixture thereof and formaldehyde; and
c) a solvent component in the amount of 35-79% by wt . , all foregoing weight percentages being based on the total weight of the coating composition; and
the coating composition being substantially free of bisphe- nol-A-diglycidyl ether, bisphenol-F-diglycidyl ether, homo- logues thereof, and polyvinyl chloride.
2. The coating compositon of claim 1 further comprising at least one lubricant.
3. The coating composition of claim 2 wherein said lubricant comprises polyethylene, polypropylene, tetrafluor ethylene or a mixture of these.
4. The coating composition of any of claims 1-3 wherein said polyester resin comprises trimethylolpropane in the amount of 0.1-10% by wt . , neopentylglycol in the amount of 15-30% by wt., at least one other polyol in the amount of 5-20% by wt., a phthalic acid in the amount of 20-60% by wt., and adipic acid in the amount of 10-35% by wt .
5. The coating composition of any of claims 1-4 wherein said solvent comprises an aromatic hydrocarbon, a glycolether/ glycolether acetate, n-butanol, an aromatic hydrocarbon, a glycolether/glycolether acetate, an alcohol, an ester, or a mixture thereof .
6. The coating composition of any of claims 1-5 comprising: a polyester resin dispersed in a solvent (2-50% by wt . ) ; a resol resin dissolved in a solvent (1-15% by wt.); a lubricant in solid form dispersed in at least one solvent (0.1-2% by wt . ) ; an acidic catalyst (0-2% by wt . ) ; and said solvent or solvents being operative to solvate said resins and lubricant; all percentages based on the total weight of the coating composition.
7. The coating compositions of claim 6 wherein said polyester and said resol resin are combined together using at least two different solvents.
8. The coating composition of any of claims 1-7 wherein said coating is coated onto a metal substrate.
9. The coating composition of claim 1 wherein said polyester resin comprises trimethylolpropane and neopentylglycol; said resol resin comprises a condensation resin made from bisphenol A, butyl phenol, xylenol or a mixture thereof and formaldehyde; at least one lubricant comprising polyethylene, polypropylene, PTFE, lanoline, carnauba wax, petrolatum, or a mixture thereof; and at least two different solvents.
10. The coating composition of claim 9 wherein at least one of the said two different solvents comprises an aromatic hydrocarbon type solvent.
11. The coating composition of any of claims 1-10 wherein said composition comprises at least two different solvents having different boiling ranges.
12. A coated metal substrate comprising a metal sheet having the coating composition of any of claims 1-11.
13. A coated can body having the coating composition according to any of claims 1-11.
14. The coating composition of claim 1 further comprising at least one catalyst.
PCT/EP2000/001065 1999-03-16 2000-02-10 Badge-free can coating WO2000055265A1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
AU26715/00A AU2671500A (en) 1999-03-16 2000-02-10 Badge-free can coating
EP00905046A EP1163305A1 (en) 1999-03-16 2000-02-10 Badge-free can coating
JP2000605687A JP2002539319A (en) 1999-03-16 2000-02-10 BADGE-free can coating
CA002363482A CA2363482A1 (en) 1999-03-16 2000-02-10 Badge-free can coating

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE1999112794 DE19912794A1 (en) 1999-03-16 1999-03-16 BADGE-free can coating
DE19912794.8 1999-03-16

Publications (1)

Publication Number Publication Date
WO2000055265A1 true WO2000055265A1 (en) 2000-09-21

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US8835012B2 (en) 2004-10-20 2014-09-16 Valspar Sourcing, Inc. Coating compositions for aluminum beverage cans and methods of coating same
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CN107936428A (en) * 2017-12-13 2018-04-20 郑州莉迪亚医药科技有限公司 Good plastics of a kind of resistance to low temperature and preparation method thereof
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JP4679077B2 (en) * 2003-06-02 2011-04-27 パイロットインキ株式会社 Liquid composition for discolored body and discolored body set using the same
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WO2003008512A1 (en) 2001-07-20 2003-01-30 Dsm Ip Assets B.V. Bisphenol a diglycidyl ether-free coating composition for metal substrates
US10829663B2 (en) 2002-08-01 2020-11-10 The Sherwin-Williams Company Coating composition for metal substrates
US10273380B2 (en) 2002-08-01 2019-04-30 The Sherwin-Williams Company Coating composition for metal substrates
US9550913B2 (en) 2002-08-01 2017-01-24 Valspar Sourcing, Inc. Coating composition for metal substrates
US8765241B2 (en) 2002-08-01 2014-07-01 Valspar Sourcing, Inc. Polyester coating composition for metal substrates comprising oxirane-functional acrylic resin
EP1584667A1 (en) * 2004-04-08 2005-10-12 Surface Specialties Austria GmbH Blends comprising phenolic resins for internal protection coatings
US8835012B2 (en) 2004-10-20 2014-09-16 Valspar Sourcing, Inc. Coating compositions for aluminum beverage cans and methods of coating same
US10336909B2 (en) 2004-10-20 2019-07-02 The Sherwin-Williams Company Coating compositions for aluminum beverage cans and methods of coating same
US9862854B2 (en) 2004-10-20 2018-01-09 Valspar Sourcing, Inc. Coating compositions for aluminum beverage cans and methods of coating same
US9415900B2 (en) 2004-10-20 2016-08-16 Valspar Sourcing, Inc. Coating compositions for aluminum beverage cans and methods of coating same
US9446430B2 (en) 2005-08-11 2016-09-20 Valspar Sourcing, Inc. Bisphenol A and aromatic glycidyl ether-free coatings
EP2447059B1 (en) 2005-08-11 2018-05-30 Valspar Sourcing, Inc. Bisphenol A and aromatic glycidyl ether-free coatings
US10625301B2 (en) 2005-08-11 2020-04-21 Swimc Llc Bisphenol A and aromatic glycidyl ether-free coatings
US8632857B2 (en) 2005-08-11 2014-01-21 Valspar Sourcing, Inc. Bisphenol A and aromatic glycidyl ether-free coatings
US8197904B2 (en) 2005-08-11 2012-06-12 Valspar Sourcing, Inc. Bisphenol A and aromatic glycidyl ether-free coatings
US8142858B2 (en) 2005-08-11 2012-03-27 Valspar Sourcing, Inc. Bisphenol A and aromatic glycidyl ether-free coatings
US9993842B2 (en) 2005-08-11 2018-06-12 Swimc Llc Bisphenol A and aromatic glycidyl ether-free coatings
CN101316892B (en) * 2005-11-29 2012-01-04 格雷斯公司 Paint for pot not containing BADGE and BPA
WO2007062735A1 (en) 2005-11-29 2007-06-07 W.R. Grace & Co.-Conn. Badge- and bpa-free can coating
WO2008101590A1 (en) * 2007-02-22 2008-08-28 Cytec Surface Specialties Austria Gmbh Coating compositions for can coating comprising phenolic resins
US9115241B2 (en) 2010-04-01 2015-08-25 Ppg Industries Ohio, Inc. Branched polyester polymers and soft touch coatings comprising the same
US9695264B2 (en) 2010-04-01 2017-07-04 Ppg Industries Ohio, Inc. High functionality polyesters and coatings comprising the same
US10035872B2 (en) 2010-04-01 2018-07-31 Ppg Industries Ohio, Inc. Branched polyester-urethane resins and coatings comprising the same
WO2011123610A1 (en) * 2010-04-01 2011-10-06 Ppg Industries Ohio, Inc. High functionality polyesters and coatings comprising the same
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US9187213B2 (en) 2010-10-15 2015-11-17 Valspar Sourcing, Inc. Polyester-based coating composition for metal substrates
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CN107936428A (en) * 2017-12-13 2018-04-20 郑州莉迪亚医药科技有限公司 Good plastics of a kind of resistance to low temperature and preparation method thereof

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AU2671500A (en) 2000-10-04
MXPA01009010A (en) 2002-01-01

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