EP0809572A1 - Protective polymeric film for lamination to metal - Google Patents
Protective polymeric film for lamination to metalInfo
- Publication number
- EP0809572A1 EP0809572A1 EP96906379A EP96906379A EP0809572A1 EP 0809572 A1 EP0809572 A1 EP 0809572A1 EP 96906379 A EP96906379 A EP 96906379A EP 96906379 A EP96906379 A EP 96906379A EP 0809572 A1 EP0809572 A1 EP 0809572A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- scratch
- layer
- percent
- ethylene
- resistant layer
- Prior art date
- Legal status (The legal status 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 status listed.)
- Withdrawn
Links
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 70
- 239000002184 metal Substances 0.000 title claims abstract description 70
- 230000001681 protective effect Effects 0.000 title claims abstract description 47
- 238000003475 lamination Methods 0.000 title description 3
- 239000010410 layer Substances 0.000 claims abstract description 117
- 230000003678 scratch resistant effect Effects 0.000 claims abstract description 63
- 239000012790 adhesive layer Substances 0.000 claims abstract description 41
- 239000000758 substrate Substances 0.000 claims abstract description 24
- 239000000443 aerosol Substances 0.000 claims abstract description 23
- -1 propylene, ethylene-propylene Chemical group 0.000 claims description 46
- 239000004743 Polypropylene Substances 0.000 claims description 28
- 239000000203 mixture Substances 0.000 claims description 28
- 229920001155 polypropylene Polymers 0.000 claims description 28
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 26
- 239000005977 Ethylene Substances 0.000 claims description 26
- 229920001577 copolymer Polymers 0.000 claims description 18
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 16
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 16
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 15
- 230000001070 adhesive effect Effects 0.000 claims description 15
- 239000000853 adhesive Substances 0.000 claims description 14
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 12
- 239000004952 Polyamide Substances 0.000 claims description 12
- 239000004698 Polyethylene Substances 0.000 claims description 12
- 229920002647 polyamide Polymers 0.000 claims description 12
- 229920000573 polyethylene Polymers 0.000 claims description 12
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 11
- 229920001519 homopolymer Polymers 0.000 claims description 10
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 10
- 239000004814 polyurethane Substances 0.000 claims description 9
- 229920002635 polyurethane Polymers 0.000 claims description 9
- 238000000576 coating method Methods 0.000 claims description 7
- 229920005989 resin Polymers 0.000 claims description 7
- 239000011347 resin Substances 0.000 claims description 7
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 6
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims description 6
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 6
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 6
- 229920000554 ionomer Polymers 0.000 claims description 6
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims description 6
- 229920000728 polyester Polymers 0.000 claims description 6
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 claims description 5
- 229920000181 Ethylene propylene rubber Polymers 0.000 claims description 4
- 229920006132 styrene block copolymer Polymers 0.000 claims description 4
- 238000012360 testing method Methods 0.000 claims description 4
- 239000004593 Epoxy Substances 0.000 claims description 3
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 3
- 239000011256 inorganic filler Substances 0.000 claims description 3
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 3
- 229920001296 polysiloxane Polymers 0.000 claims description 3
- 239000011248 coating agent Substances 0.000 claims description 2
- 230000001747 exhibiting effect Effects 0.000 claims 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 239000002904 solvent Substances 0.000 abstract description 14
- 238000005260 corrosion Methods 0.000 abstract description 13
- 230000007797 corrosion Effects 0.000 abstract description 13
- 230000003213 activating effect Effects 0.000 abstract description 3
- 235000019589 hardness Nutrition 0.000 description 14
- 239000000126 substance Substances 0.000 description 13
- 229910000831 Steel Inorganic materials 0.000 description 9
- 239000010959 steel Substances 0.000 description 9
- 229920000092 linear low density polyethylene Polymers 0.000 description 7
- 239000004707 linear low-density polyethylene Substances 0.000 description 7
- 238000005299 abrasion Methods 0.000 description 6
- 229920001862 ultra low molecular weight polyethylene Polymers 0.000 description 6
- 229940038553 attane Drugs 0.000 description 4
- 229920005629 polypropylene homopolymer Polymers 0.000 description 4
- 239000011241 protective layer Substances 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 229920003300 Plexar® Polymers 0.000 description 3
- 239000002313 adhesive film Substances 0.000 description 3
- 229920001903 high density polyethylene Polymers 0.000 description 3
- 239000004700 high-density polyethylene Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 239000002666 chemical blowing agent Substances 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 229920006285 olefinic elastomer Polymers 0.000 description 2
- 229920006254 polymer film Polymers 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 229920005672 polyolefin resin Polymers 0.000 description 2
- 229920005630 polypropylene random copolymer Polymers 0.000 description 2
- 230000000750 progressive effect Effects 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- CLJTZNIHUYFUMR-UHFFFAOYSA-M sodium;hydrogen carbonate;2-hydroxypropane-1,2,3-tricarboxylic acid Chemical compound [Na+].OC([O-])=O.OC(=O)CC(O)(C(O)=O)CC(O)=O CLJTZNIHUYFUMR-UHFFFAOYSA-M 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- 239000005029 tin-free steel Substances 0.000 description 2
- ZPEZUAAEBBHXBT-WCCKRBBISA-N (2s)-2-amino-3-methylbutanoic acid;2-amino-3-methylbutanoic acid Chemical compound CC(C)C(N)C(O)=O.CC(C)[C@H](N)C(O)=O ZPEZUAAEBBHXBT-WCCKRBBISA-N 0.000 description 1
- 239000004156 Azodicarbonamide Substances 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 239000004708 Very-low-density polyethylene Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000002998 adhesive polymer Substances 0.000 description 1
- 239000004840 adhesive resin Substances 0.000 description 1
- 229920006223 adhesive resin Polymers 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 1
- 235000019399 azodicarbonamide Nutrition 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000012968 metallocene catalyst Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000012766 organic filler Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 239000013047 polymeric layer Substances 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 229920001866 very low density polyethylene Polymers 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B15/00—Layered products comprising a layer of metal
- B32B15/04—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B15/08—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B15/00—Layered products comprising a layer of metal
- B32B15/04—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B15/08—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
- B32B15/085—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin comprising polyolefins
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B15/00—Layered products comprising a layer of metal
- B32B15/04—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B15/08—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
- B32B15/088—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin comprising polyamides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B15/00—Layered products comprising a layer of metal
- B32B15/04—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B15/08—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
- B32B15/09—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin comprising polyesters
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
- B32B27/20—Layered products comprising a layer of synthetic resin characterised by the use of special additives using fillers, pigments, thixotroping agents
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
- B32B27/302—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising aromatic vinyl (co)polymers, e.g. styrenic (co)polymers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/40—Layered products comprising a layer of synthetic resin comprising polyurethanes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/04—Interconnection of layers
- B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B38/00—Ancillary operations in connection with laminating processes
- B32B2038/0052—Other operations not otherwise provided for
- B32B2038/0076—Curing, vulcanising, cross-linking
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/50—Properties of the layers or laminate having particular mechanical properties
- B32B2307/584—Scratch resistance
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2311/00—Metals, their alloys or their compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2323/00—Polyalkenes
- B32B2323/04—Polyethylene
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2323/00—Polyalkenes
- B32B2323/10—Polypropylene
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2325/00—Polymers of vinyl-aromatic compounds, e.g. polystyrene
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2375/00—Polyureas; Polyurethanes
Definitions
- the present invention relates to a protective polymeric film which may be readily laminated to metal substrates to provide protection from scratches, solvents, and corrosion, and which exhibits good sealability and compressibility when the laminate is used to form metal containers.
- Protective polymeric films or coatings are known in the art which can be laminated to metals such as tin-free steel, tin-plated steel, and aluminum, and then formed into parts such as aerosol valve mounting cups, aerosol can domes or bottoms, paint cans, food and beverage containers, and the like. Such films or coatings are used to protect the underlying metal surface from corrosion as well as to provide resistance to solvents and abrasions.
- U.S. Patent No. 4,626,157 to Franek et al describes a method of making metal containers such as aerosol dispensing containers having top can end members and valve cup members formed from a metal laminate comprising a thin polymeric layer such as polyester or polypropylene overlaid on the metallic substrate.
- the metal/film laminates using polypropylene do not exhibit good sealability and compressibility when used to fabricate metal containers such as aerosol cans. Specifically, such films do not form a good seal for compression formed joints or seals between two pieces of a metal laminate. Such a poor seal may result in leakage of pressurized propellant from a metal aerosol container formed from the metal laminate.
- polypropylene has been found to be difficult to adhere to various metallic substrates.
- Many commercial polypropylene film laminates currently in use are adhered tometal with solvent based-adhesives such as urethane adhesives.
- solvent based-adhesives such as urethane adhesives.
- such adhesives are undesirable as they are environmentally unfriendly and leave the potential for residual solvents from the adhesive to migrate gradually through the film laminate and contaminate the contents of the metal container.
- inadequate curing of the adhesive can result in loss of adhesion of the film laminate, particularly following exposure to solvents that may be contained within the fabricated structure.
- polymer films have more recently been laminated to metal using thermoplastic adhesive resins.
- U.S. Patent No. 4,980,210 to Heyes et al describes a two-layer film bonded to the surface of a metal sheet comprising an inner adhesive layer of an acid-modified polyolefin resin and an outer layer of a polyolefin.
- U.S. Patent No. 5,006,383 to Achille et al teach a blend of polypropylene and very low density polyethylene and an adhesive layer comprising a rubber and polar comonomer modified ⁇ -olefin polymer resin.
- the films may not provide sufficient resistance to abrasions and scratches.
- such film laminates can possibly be damaged by cutting, abrading or puncturing as the metal cups vibrate or move against each other. Damage can also occur during part die stamping or forming if the stamping dies or assembly mechanisms are not perfectly aligned. If the protective polymeric film becomes damaged, the corrosion resistance of the aerosol valve mounting cups is also weakened.
- the present invention meets that need by providing a protective polymeric film which may be readily laminated to a metal substrate, which is resistant to scratches, solvents and corrosion, and which exhibits good sealability and compressibility when used to form metal containers.
- the film may be produced by conventional coextrusion techniques.
- a protective polymeric film comprising an adhesive layer comprising from 5 to 25 percent of the total film thickness, a scratch- resistant layer comprising from 5 to 40 percent of the total film thickness, and a compressible layer positioned between the adhesive and scratch-resistant layers comprising from 40-80 percent of the total film thickness.
- the scratch-resistant layer preferably has an ASTM D2240 Shore D hardness of at least 60, and the adhesive and compressible layers have a Shore D hardness which is less than that of the scratch-resistant layer. Additionally, it is desired that the scratch-resistant layer have an ASTM D3363 pencil hardness of at least 3B, and preferably at least B.
- the adhesive layer is selected from the group consisting of ethylenically unsaturated copolymers of vinyl acetate, ethyl acrylate, ethyl methacrylate, methyl acrylic acid, acrylic acid, or carbon monoxide; homopolymers of ethylene or propylene; copolymers of ethylene and propylene; ionomers of ethylene and methacrylic acid or acrylic acid; maleic anhydride modified polyethylene; polyamides; poly u ret anes; or compatible blends thereof.
- the adhesive layer is preferably thermally activated for lamination to a metal substrate and is solvent free.
- the scratch-resistant layer is preferably selected from the group consisting of polypropylene, polyethylene, polyester, polyamide, and blends thereof.
- the hard scratch resistant layer functions to protect the underlying metal from scratches, and provides resistance to solvents and corrosion.
- the scratch- resistant layer may be coated with curable hard coatings selected from the group consisting of urethane, epoxy, acrylic and silicone to provide enhanced scratch resistance properties.
- the scratch-resistant layer may also contain an inorganic filler to further harden the layer and enhance scratch resistance. Chemical or radiation-induced crosslinking may also be used to further enhance the hardness and scratch resistance properties of the scratch-resistant layer.
- the compressible layer preferably comprises homopolymers of ethylene or propylene, copolymers of ethylene and propylene, ethylene-propylene rubbers, thermoplastic olefinic elastomer resins, styrene block copolymers, polyurethane, and blends thereof.
- the compressible layer is a softer polymeric film layer which provides good sealability and compressibility properties when the protective film is laminated to a metal substrate and used to fabricate metal containers.
- the compressible layer is foamed using a chemical blowing agent to provide improved compressibility.
- the protective polymeric film of the present invention preferably has a thickness of from 0.5 to 20.0 mils (0.013 to 0.51 mm).
- the protective polymeric 0 film is bonded to at least one major surface of a metal substrate to form a metal laminate where the film comprises scratch-resistant, adhesive, and compressible layers as described above.
- Suitable metal substrates range from 5 to 100 mils (0.13 to 2.5 mm) in thickness and preferably from 5 to 15 mils (0.13 to 0.38) in thickness.
- the protective polymeric film is preferably laminated to the metal laminate by thermally activating the adhesive layer and bonding the adhesive layer to the metal 5 laminate.
- the film should exhibit at least 5.0 pounds per linear inch (.89 kg/cm) peel adhesion to the metal when subjected to a 180 degree peel test in accordance with ASTM D-903.
- the scratch- resistant layer becomes the exposed outer protective layer of the metal laminate, and the softer, compressible layer remains between the adhesive and scratch-resistant layers.
- the protective film protects the underlying metal substrate from scratches which could expose the metal to solvents and o corrosion.
- a protective polymeric film which includes a scratch resistant layer and an adjacent layer which possesses both compressible and adhesive properties.
- the compressible adhesive layer comprises from 10 to 90 percent of the total film thickness and the scratch-resistant layer comprises from 10 to 90 percent of the total film 5 thickness.
- the scratch-resistant layer has a Shore D hardness of at least 60, and the compressible adhesive layer has a Shore 0 hardness which is less than that of the scratch-resistant layer. Additionally, it is desired that the scratch-resistant layer have an ASTM D3363 pencil hardness of at least 3B, and preferably at least B.
- the compressible adhesive layer is preferably selected from the group consisting of o ethylenically unsaturatedcopolymers of vinyl acetate, ethyl acrylate, ethyl methacrylate, methyl acrylic acid, acrylic acid, carbon monoxide, homopolymers of ethylene or propylene, copolymers of ethylene and propylene, ionomers of ethylene and methyl acrylic acid or acrylic acid, grafted anhydride copolymers, polyamides, polyurethanes, and compatible blends thereof.
- the compressible adhesive layer is foamed.
- the scratch-resistant layer is preferably selected from the group consisting of polypropylene, polyethylene, polyester, polyamide, or blends thereof.
- the scratch resistant layer may be coated with curable coatings, crosslinked, or may include organic fillers as described above to provide enhanced scratch resistance.
- the protective polymeric film of the present invention can be laminated to metals such as tin- free steel, tin-plated steel, and aluminum. In one embodiment of the invention, the protective polymeric film is laminated to tin-plated steel to form an aerosol valve mounting cup.
- the protective film of the present invention can also be fabricated into a number of other parts including aerosol can domes, can bottoms, paint cans, metal trays, pans and the like.
- a protective polymeric film whic may be laminated to a metal substrate. It is a further feature of the invention to provide a protective polymeric film which provides resistance to scratches, solvents and corrosion, and which exhibits good sealability and compressibility when used in the fabrication of metal containers.
- Fig. 1 is a cross-sectional view of the protective polymeric film of the present invention showing scratch-resistant, compressible, and adhesive layers;
- Fig. 2 is a cross-sectional view of an alternative embodiment of the protective film comprising scratch-resistant and compressible adhesive layers;
- Fig. 3 is a variation of the embodiment shown in Fig. 1 in which the film has been laminated t a metal substrate;
- Fig. 4 is a perspective view of an aerosol valve mounting cup which has been formed from the protective film of the present invention.
- the protective polymeric film and film/metal laminate of the present invention provides a combination of properties which has not been achieved by prior art protective films.
- the present invention utilizes a soft film layer which exhibits good compressibility and sealing properties in combination with a hard film layer which resists nicks and abrasions which could expose the underlying metal surface and subject it to corrosion.
- the film of the present invention may be readily laminated to a metal substrate by thermally activating a solvent-free adhesive film layer, and the resulting metal laminate may be formed into metal containers which are protected from scratches, solvents and corrosion. The bond formed between the adhesive film layer and metal substrate is strong and durable.
- the laminate of the present invention can resist delamination or debonding of the film from the metal substrate after 30 days of immersion in methylene chloride.
- the protective polymeric film of the present invention may comprise either a 3-layer film comprising adhesive, compressible, and scratch-resistant layers, or a two-layer film comprising a scratch-resistant layer and an adjacent layer having both compressible and adhesive properties.
- the film includes a scratch-resistant layer 10, an adhesive layer 14, and a compressible layer 12 positioned between the scratch-resistant layer and the adhesive layer.
- the scratch resistant layer exhibits a Shore D durometer hardness of at least 60 as tested according to ASTM D2240. A pencil scratch resistance of at least a "3B" rating according to ASTM D3363 is also preferable.
- Films suitable for use as the scratch-resistant layer include polypropylene, polyethylene, polyester, polyamide, and blends thereof having the requisite hardness. Although olefin resins such as polypropylene and polyethylene are preferred, other suitable resins include polyester and polyamide or nylon resins. However, it is preferred that the scratch-resistant layer should be comprised of greater than 80 percent polypropylene to provide the desired scratch resistance properties.
- the scratch-resistant layer 10 may be coated with hard curable coatings such as urethanes, epoxy, acrylic or silicones to provide enhanced surface scratch or abrasion resistance.
- hard curable coatings such as urethanes, epoxy, acrylic or silicones to provide enhanced surface scratch or abrasion resistance.
- Additives such as inorganic fillers or chemical or radiation induced crosslinking may also be used to further enhance the hardness and scratch resistance of the scratch-resistant layer.
- the compressible layer 12 may be produced from homopolymers of ethylene or propylene, copolymers of ethylene and propylene, ethylene-propylene or other olefinic rubbers.
- Thermoplastic elastomers such as styrenic block copolymers, polyurethane, or blends of these resins are also suitable for use in the present invention.
- the compressible layer is preferably foamed using chemical blowing agents such as sodium bicarbonate-citric acid blends or azodicarbonamide. The foamed compressible layer provides improved compressibility over a conventionally extruded solid layer.
- Suitable adhesive polymers useful as the adhesive layer 14 include, but are not limited to, ethylenically unsaturated copolymers of vinyl acetate, ethyl acrylate, ethyl methacrylate, methyl acrylic acid, acrylic acid, and carbon monoxide.
- Other examples include homopolymers of ethylene or propylene, copolymers of ethylene and propylene, ionomers of ethylene and methyl acrylic acid or acrylic acid, grafted anhydride copolymers, polyamides, polyurethanes, and compatible blends thereof.
- the adhesive layer should be readily adherable to the compressible layer as well as to a metal substrate.
- the scratch-resistant layer comprises from 5-40 percent of the total film thickness
- the compressible layer comprises from 40-80 percent of the total film thickness
- the adhesive layer comprises 5-25 percent of the total film thickness.
- a more preferred structure for the 3-layer film is a scratch-resistant layer comprising 20 percent of the total thickness, a compressible layer comprising 65 percent of the total thickness, and an adhesive layer comprising 15 percent of the total thickness.
- FIG. 2 An alternative embodiment of the invention is illustrated in Fig. 2 in which the film comprises compressible adhesive layer 16 and a scratch resistant layer 10.
- the compressible adhesive layer preferably comprises 75 percent of the total film thickness and the scratch-resistant layer comprises 25 percent of the total film thickness.
- the scratch-resistant layer may comprise polypropylene, polyethylene, polyester, polyamide, and blends thereof, with polypropylene being the most preferred.
- Suitable resins for use as the compressible adhesive layer include ethylenically unsaturated copolymers of vinyl acetate, ethyl acrylate, ethyl methacrylate, methyl acrylic acid, acrylic acid, carbon monoxide, homopolymers of ethylene or propylene, copolymers of ethylene and propylene, ionomers of ethylene and methyl acryli acid or acrylic acid, grafted anhydride copolymers, polyamides, polyurethanes, and compatible blend thereof.
- the protective polymeric film of the present invention is preferably produced by a coextrusio process on a conventional cast film line or tubular blown film line.
- the layers may be coextruded together, and the resulting protective film may then be thermally laminated to a metal substrate using a hot roll laminator.
- a metal laminate is shown in Fig. 3 in which adhesive layer 14 is adhered to a metal substrate 18 with the scratch-resistant layer 10 forming an outer protective layer for the metal.
- the metal can be coated on one or both sides with the same or different protective films.
- Fig. 4 illustrates an aerosol valve mounting cup 20 formed by stamping the metal laminate formed from the protective film of the present invention.
- the compressible layer 12 allows the film to be readily compressed for fabricating such parts, and also provides a good seal, such as during crimping operations when the aerosol valve mounting cup is later crimped to a can body.
- the protective film may be laminated to both sides of a metal substrate.
- the film thickness may be from 5-10 mils (0.13 mm - 0.25 mm) on the inside of an aerosol valve mounting cup, forming a sealing gasket, and from 1 -2 mils (0.025 mm - 0.05 mm) on the outside of the cup, forming a scratch resistant, corrosion resistant coating.
- a three-layer protective polymeric film was produced in accordance with the present invention on a conventional cast film line.
- the scratch-resistant layer which comprised 25 percent of the total film thickness, was comprised of a polypropylene homopolymer (Himont ProFaxTM PD-064).
- the compressible layer comprised 60 percent of the total film thickness and was comprised of a blend of 50 percent polypropylene (Himont ProFaxTM PD-064) and 50 percent ultra low density polyethylene (Dow Chemical ATTANE® 4201).
- the adhesive layer comprised 15 percent of the total film thickness and was comprised of a blend of 60 percent Quantum Chemical PlexarTM 360 maleic anhydride modified linear low density polyethylene and 40 percent Quantum Chemical PlexarTM 206 maleic anhydride modified high density polyethylene.
- Each layer was extruded at temperatures of 400-410°F (204-210°C) with a die temperature of 410°F (210°C).
- the coextruded film was quenched on a 100°F (38°C) casting roll and then wound into a roll.
- the resulting 8.0 mil (0.2 mm) thick film was then thermally laminated to a 10.5 mil (0.27 mm) tin-plated steel at 350°F (177°C) using a hot roll laminator.
- the film exhibited peel adhesion greater than 10.0 pounds per linear inch (1.8 kg/cm) when subjected to 180 degree peel testing using an Instron tensile tester (ASTM D-903).
- ASTM D-903 Instron tensile tester
- a three-layer 8.0 mil (0.2 mm) thick coextruded film was produced on conventional cast film line.
- the outermost scratch resistant layer which was 25 percent of the total film gauge, was comprised of a polypropylene random copolymer (Himont Profax 7531).
- the compressible layer 60 percent of film gauge was comprised of a blend of 50 percent polypropylene random copolymer (Himont Profax 7531) and 50 percent ultra low density polyethylene (Dow Chemical ATTANE 4202).
- the adhesive layer (15 percent of film gauge) was comprised of a blend of 60 percent Quantum
- Example 2 Another 8.0 mil (0.2 mm) three-layer protective polymeric film was prepared as in Example 1.
- the scratch-resistant layer comprised 25 percent of the total film thickness and was comprised of a polypropylene homopolymer (Himont ProFaxTM PD-064).
- the compressible layer comprised 60 percent of the total film thickness and was comprised of a very low density metallocene catalyst ethylene copolymer (Dow AFFINITY® PL-1840).
- the adhesive layer comprised 15 percent of the total film thickness and was comprised of 100 percent Quantum Chemical PlexarTM 360 maleic 5 anhydride modified linear low density polyethylene.
- Eachlayer was coextruded as described in
- Example 1 and the resulting film was quenched and thermally laminated to a 10.5 mil (0.27 mm) tin- plated steel.
- a three-layer protective polymeric film was prepared as in Example 1.
- the scratch-resistant l o layer (25 percent of total film thickness) was comprised of a polypropylene homopolymer (Himont ProFaxTM PD-064).
- the compressible layer (60 percent of total film thickness) was comprised of a blend of 50 percent polypropylene (Himont ProFaxTM PD-191) and 50 percent ultra low density polyethylene (Dow Chemical ATTANE® 4201) with a 1.5 phr of a sodium bicarbonate-citric acid based foam concentrate (Henley HydrocerolTM CF-20).
- the endothermic blowing agent was 15 activated during extrusion to produce a very fine closed cell foam compressible layer.
- the adhesive layer (15 percent of total film thickness) was comprised of 100 percent Quantum Chemical PlexarTM 360 maleic anhydride modified linear low density polyethylene. Each layer was extruded as described in Example 1 , and the resulting film was quenched and thermally laminated to a 10.5 mil (0.27 mm) tin-plated steel.
- a three-layer protective polymeric film was prepared as in Example 1 comprising a scratch- resistant layer (25 percent of total film thickness) of a polypropylene homopolymer (Himont ProFaxTM PD-064), a compressible layer (60 percent of total film thickness) comprising a blend of 65 percent polypropylene (Himont ProFaxTM PD-064) and 35 percent ethylene-propylene rubber (Exxon 25 Chemical VistalonTM 3708P).
- the adhesive layer was comprised of 100 percent Quantum Chemical PlexarTM 360 maleic anhydride modified linear low density polyethylene. Each layer was extruded as in Example 1, and the resulting film was quenched and thermally laminated to tin-plated steel.
- a two-layer 8.0 mil (0.2 mm) thick polymer film was produced on a conventional cast film line.
- the scratch-resistant layer comprised 80 percent of the total film thickness and was comprised of a 50 percent polypropylene (ProFaxTM PD-064) and 50 percent ultra low density polyethylene blend (ATTANE® 4201).
- the adhesive layer comprised 20 percent of the total film thickness and was comprised of a blend of 60 percent PlexarTM 360 linear low density polyethylene and 40 percent PlexarTM 206 high density polyethylene. The resulting film was thermally laminated to tin-plated steel
- a pencil hardness test (ASTM D-3363) was used to determine scratch resistance of the plaques in Example 7.
- the plaques containing polypropylene or blends of polypropylene and ultra low density polyethylene exhibit the highest scratch resistance.
- aerosol valve mounting cups produced from the laminates described in Example 1 and Example 6, respectively were subjected to a vibratory shaker evaluation.
- Five aerosol valve mounting cups of each sample were placed into empty glass 9 oz. bottles which were mounted on a Lab-Line Instruments Multi-Wrist Shaker.
- the five identical metal laminate mounting cups in each of the bottles were subjected to vigorous shaking at an instrument setting of 10 (maximum) for five minutes.
- Cups were then removed and inspected for damage in the form of nicks, scratches or abrasion on the film laminate side using a 10X optical magnifying lupe.
- the cups of Example 6 50 percent polypropylene - 50 percent ultra low density polyethylene top layer
- the cups of Example 1 100 percent polypropylene top layer
Landscapes
- Laminated Bodies (AREA)
- Containers And Packaging Bodies Having A Special Means To Remove Contents (AREA)
Abstract
The present invention provides a protective polymeric film which can be laminated to metal substrate (18) and which provides protection against scratches, solvents and corrosion. The film also exhibits good compressibility and sealability when used to form metal containers such as aerosol valve mounting cups, can domes, bodies, bottoms, and the like. The protective polymeric film includes a scratch-resistant layer (10) having a Shore D hardness of at least 60, an adhesive layer (14), and a compressible layer (12) positioned between the scratch-resistant and adhesive layers. In an alternative embodiment, the protective film includes a scratch-resistant layer and an adjacent compressible adhesive layer. The film may be laminated to a metal substrate by thermally activating the adhesive layer.
Description
PROTECTIVE POLYMERIC FILM FOR LAMINATION TO METAL
The present invention relates to a protective polymeric film which may be readily laminated to metal substrates to provide protection from scratches, solvents, and corrosion, and which exhibits good sealability and compressibility when the laminate is used to form metal containers.
Protective polymeric films or coatings are known in the art which can be laminated to metals such as tin-free steel, tin-plated steel, and aluminum, and then formed into parts such as aerosol valve mounting cups, aerosol can domes or bottoms, paint cans, food and beverage containers, and the like. Such films or coatings are used to protect the underlying metal surface from corrosion as well as to provide resistance to solvents and abrasions. For example, U.S. Patent No. 4,626,157 to Franek et al, describes a method of making metal containers such as aerosol dispensing containers having top can end members and valve cup members formed from a metal laminate comprising a thin polymeric layer such as polyester or polypropylene overlaid on the metallic substrate.
However, while such films provide resistance to corrosion, solvents and abrasions, due to the high modulus of the polypropylene film, the metal/film laminates using polypropylene do not exhibit good sealability and compressibility when used to fabricate metal containers such as aerosol cans. Specifically, such films do not form a good seal for compression formed joints or seals between two pieces of a metal laminate. Such a poor seal may result in leakage of pressurized propellant from a metal aerosol container formed from the metal laminate.
Further, polypropylene has been found to be difficult to adhere to various metallic substrates. Many commercial polypropylene film laminates currently in use are adhered tometal with solvent based-adhesives such as urethane adhesives. However, such adhesives are undesirable as they are environmentally unfriendly and leave the potential for residual solvents from the adhesive to migrate gradually through the film laminate and contaminate the contents of the metal container. Additionally, inadequate curing of the adhesive can result in loss of adhesion of the film laminate, particularly following exposure to solvents that may be contained within the fabricated structure. As a result, polymer films have more recently been laminated to metal using thermoplastic adhesive resins. For example, U.S. Patent No. 4,980,210 to Heyes et al describes a two-layer film bonded to the surface of a metal sheet comprising an inner adhesive layer of an acid-modified polyolefin resin and an outer layer of a polyolefin.
In an attempt to solve the sealability and compressibility problems associated with prior polypropylene adhesive films, U.S. Patent No. 5,006,383 to Achille et al teach a blend of polypropylene and very low density polyethylene and an adhesive layer comprising a rubber and polar comonomer modified α-olefin polymer resin. However, while such films exhibit good compressibility and formability, the films may not provide sufficient resistance to abrasions and scratches. For example, during handling, bulk packaging, and shipping of aerosol valve mounting cups, such film laminates can possibly be damaged by cutting, abrading or puncturing as the metal cups vibrate or
move against each other. Damage can also occur during part die stamping or forming if the stamping dies or assembly mechanisms are not perfectly aligned. If the protective polymeric film becomes damaged, the corrosion resistance of the aerosol valve mounting cups is also weakened.
Accordingly, there is still a need in the art for a protective film which may be readily laminated to a metal substrate without the use of a solvent-based adhesive, which exhibits good sealability and compressibility, and which is scratch resistant as well as resistant to solvents and corrosion.
The present invention meets that need by providing a protective polymeric film which may be readily laminated to a metal substrate, which is resistant to scratches, solvents and corrosion, and which exhibits good sealability and compressibility when used to form metal containers. The film may be produced by conventional coextrusion techniques.
According to one aspect of the present invention, a protective polymeric film is provided comprising an adhesive layer comprising from 5 to 25 percent of the total film thickness, a scratch- resistant layer comprising from 5 to 40 percent of the total film thickness, and a compressible layer positioned between the adhesive and scratch-resistant layers comprising from 40-80 percent of the total film thickness. The scratch-resistant layer preferably has an ASTM D2240 Shore D hardness of at least 60, and the adhesive and compressible layers have a Shore D hardness which is less than that of the scratch-resistant layer. Additionally, it is desired that the scratch-resistant layer have an ASTM D3363 pencil hardness of at least 3B, and preferably at least B.
Preferably, the adhesive layer is selected from the group consisting of ethylenically unsaturated copolymers of vinyl acetate, ethyl acrylate, ethyl methacrylate, methyl acrylic acid, acrylic acid, or carbon monoxide; homopolymers of ethylene or propylene; copolymers of ethylene and propylene; ionomers of ethylene and methacrylic acid or acrylic acid; maleic anhydride modified polyethylene; polyamides; poly u ret anes; or compatible blends thereof. The adhesive layer is preferably thermally activated for lamination to a metal substrate and is solvent free.
The scratch-resistant layer is preferably selected from the group consisting of polypropylene, polyethylene, polyester, polyamide, and blends thereof. Once the protective film is laminated to a metal substrate, the hard scratch resistant layer functions to protect the underlying metal from scratches, and provides resistance to solvents and corrosion. Optionally, the scratch- resistant layer may be coated with curable hard coatings selected from the group consisting of urethane, epoxy, acrylic and silicone to provide enhanced scratch resistance properties.
The scratch-resistant layer may also contain an inorganic filler to further harden the layer and enhance scratch resistance. Chemical or radiation-induced crosslinking may also be used to further enhance the hardness and scratch resistance properties of the scratch-resistant layer.
The compressible layer preferably comprises homopolymers of ethylene or propylene, copolymers of ethylene and propylene, ethylene-propylene rubbers, thermoplastic olefinic elastomer resins, styrene block copolymers, polyurethane, and blends thereof. The compressible layer is a softer polymeric film layer which provides good sealability and compressibility properties when the protective film is laminated to a metal substrate and used to fabricate metal containers. In a preferred embodiment of the invention, the compressible layer is foamed using a chemical blowing agent to provide improved compressibility.
The protective polymeric film of the present invention preferably has a thickness of from 0.5 to 20.0 mils (0.013 to 0.51 mm). In a preferred embodiment of theinvention, the protective polymeric 0 film is bonded to at least one major surface of a metal substrate to form a metal laminate where the film comprises scratch-resistant, adhesive, and compressible layers as described above. Suitable metal substrates range from 5 to 100 mils (0.13 to 2.5 mm) in thickness and preferably from 5 to 15 mils (0.13 to 0.38) in thickness. The protective polymeric film is preferably laminated to the metal laminate by thermally activating the adhesive layer and bonding the adhesive layer to the metal 5 laminate. The film should exhibit at least 5.0 pounds per linear inch (.89 kg/cm) peel adhesion to the metal when subjected to a 180 degree peel test in accordance with ASTM D-903. Thus, the scratch- resistant layer becomes the exposed outer protective layer of the metal laminate, and the softer, compressible layer remains between the adhesive and scratch-resistant layers. The protective film protects the underlying metal substrate from scratches which could expose the metal to solvents and o corrosion.
In an alternative embodiment of the invention, a protective polymeric film is provided which includes a scratch resistant layer and an adjacent layer which possesses both compressible and adhesive properties. The compressible adhesive layer comprises from 10 to 90 percent of the total film thickness and the scratch-resistant layer comprises from 10 to 90 percent of the total film 5 thickness. The scratch-resistant layer has a Shore D hardness of at least 60, and the compressible adhesive layer has a Shore 0 hardness which is less than that of the scratch-resistant layer. Additionally, it is desired that the scratch-resistant layer have an ASTM D3363 pencil hardness of at least 3B, and preferably at least B.
The compressible adhesive layer is preferably selected from the group consisting of o ethylenically unsaturatedcopolymers of vinyl acetate, ethyl acrylate, ethyl methacrylate, methyl acrylic acid, acrylic acid, carbon monoxide, homopolymers of ethylene or propylene, copolymers of ethylene and propylene, ionomers of ethylene and methyl acrylic acid or acrylic acid, grafted anhydride copolymers, polyamides, polyurethanes, and compatible blends thereof. Preferably, the compressible adhesive layer is foamed.
5 The scratch-resistant layer is preferably selected from the group consisting of polypropylene, polyethylene, polyester, polyamide, or blends thereof. The scratch resistant layer may be coated with
curable coatings, crosslinked, or may include organic fillers as described above to provide enhanced scratch resistance.
The protective polymeric film of the present invention can be laminated to metals such as tin- free steel, tin-plated steel, and aluminum. In one embodiment of the invention, the protective polymeric film is laminated to tin-plated steel to form an aerosol valve mounting cup. The protective film of the present invention can also be fabricated into a number of other parts including aerosol can domes, can bottoms, paint cans, metal trays, pans and the like.
Accordingly, it is a feature of the present invention to provide a protective polymeric film whic may be laminated to a metal substrate. It is a further feature of the invention to provide a protective polymeric film which provides resistance to scratches, solvents and corrosion, and which exhibits good sealability and compressibility when used in the fabrication of metal containers. These, and other features and advantages of the present invention, will become apparent from the following detailed description, the accompanying drawings, and the appended claims.
Fig. 1 is a cross-sectional view of the protective polymeric film of the present invention showing scratch-resistant, compressible, and adhesive layers;
Fig. 2 is a cross-sectional view of an alternative embodiment of the protective film comprising scratch-resistant and compressible adhesive layers;
Fig. 3 is a variation of the embodiment shown in Fig. 1 in which the film has been laminated t a metal substrate; and
Fig. 4 is a perspective view of an aerosol valve mounting cup which has been formed from the protective film of the present invention.
The protective polymeric film and film/metal laminate of the present invention provides a combination of properties which has not been achieved by prior art protective films. The present invention utilizes a soft film layer which exhibits good compressibility and sealing properties in combination with a hard film layer which resists nicks and abrasions which could expose the underlying metal surface and subject it to corrosion. The film of the present invention may be readily laminated to a metal substrate by thermally activating a solvent-free adhesive film layer, and the resulting metal laminate may be formed into metal containers which are protected from scratches, solvents and corrosion. The bond formed between the adhesive film layer and metal substrate is strong and durable. Depending on the desired end use, the laminate of the present invention can resist delamination or debonding of the film from the metal substrate after 30 days of immersion in methylene chloride.
The protective polymeric film of the present invention may comprise either a 3-layer film comprising adhesive, compressible, and scratch-resistant layers, or a two-layer film comprising a scratch-resistant layer and an adjacent layer having both compressible and adhesive properties.
Referring now to Fig. 1 , one embodiment of the protective polymeric film of the present invention is illustrated. The film includes a scratch-resistant layer 10, an adhesive layer 14, and a compressible layer 12 positioned between the scratch-resistant layer and the adhesive layer. The scratch resistant layer exhibits a Shore D durometer hardness of at least 60 as tested according to ASTM D2240. A pencil scratch resistance of at least a "3B" rating according to ASTM D3363 is also preferable. Films suitable for use as the scratch-resistant layer include polypropylene, polyethylene, polyester, polyamide, and blends thereof having the requisite hardness. Although olefin resins such as polypropylene and polyethylene are preferred, other suitable resins include polyester and polyamide or nylon resins. However, it is preferred that the scratch-resistant layer should be comprised of greater than 80 percent polypropylene to provide the desired scratch resistance properties.
The scratch-resistant layer 10 may be coated with hard curable coatings such as urethanes, epoxy, acrylic or silicones to provide enhanced surface scratch or abrasion resistance. Additives such as inorganic fillers or chemical or radiation induced crosslinking may also be used to further enhance the hardness and scratch resistance of the scratch-resistant layer.
The compressible layer 12 may be produced from homopolymers of ethylene or propylene, copolymers of ethylene and propylene, ethylene-propylene or other olefinic rubbers. Thermoplastic elastomers such as styrenic block copolymers, polyurethane, or blends of these resins are also suitable for use in the present invention. The compressible layer ispreferably foamed using chemical blowing agents such as sodium bicarbonate-citric acid blends or azodicarbonamide. The foamed compressible layer provides improved compressibility over a conventionally extruded solid layer.
Suitable adhesive polymers useful as the adhesive layer 14 include, but are not limited to, ethylenically unsaturated copolymers of vinyl acetate, ethyl acrylate, ethyl methacrylate, methyl acrylic acid, acrylic acid, and carbon monoxide. Other examples include homopolymers of ethylene or propylene, copolymers of ethylene and propylene, ionomers of ethylene and methyl acrylic acid or acrylic acid, grafted anhydride copolymers, polyamides, polyurethanes, and compatible blends thereof. The adhesive layer should be readily adherable to the compressible layer as well as to a metal substrate.
Generally, the scratch-resistant layer comprises from 5-40 percent of the total film thickness, the compressible layer comprises from 40-80 percent of the total film thickness, and the adhesive layer comprises 5-25 percent of the total film thickness. A more preferred structure for the 3-layer film is a scratch-resistant layer comprising 20 percent of the total thickness, a compressible layer
comprising 65 percent of the total thickness, and an adhesive layer comprising 15 percent of the total thickness.
An alternative embodiment of the invention is illustrated in Fig. 2 in which the film comprises compressible adhesive layer 16 and a scratch resistant layer 10. In this embodiment, the compressible adhesive layer preferably comprises 75 percent of the total film thickness and the scratch-resistant layer comprises 25 percent of the total film thickness.
The scratch-resistant layer may comprise polypropylene, polyethylene, polyester, polyamide, and blends thereof, with polypropylene being the most preferred. Suitable resins for use as the compressible adhesive layer include ethylenically unsaturated copolymers of vinyl acetate, ethyl acrylate, ethyl methacrylate, methyl acrylic acid, acrylic acid, carbon monoxide, homopolymers of ethylene or propylene, copolymers of ethylene and propylene, ionomers of ethylene and methyl acryli acid or acrylic acid, grafted anhydride copolymers, polyamides, polyurethanes, and compatible blend thereof.
The protective polymeric film of the present invention is preferably produced by a coextrusio process on a conventional cast film line or tubular blown film line. The layers may be coextruded together, and the resulting protective film may then be thermally laminated to a metal substrate using a hot roll laminator. A metal laminate is shown in Fig. 3 in which adhesive layer 14 is adhered to a metal substrate 18 with the scratch-resistant layer 10 forming an outer protective layer for the metal. The metal can be coated on one or both sides with the same or different protective films.
The resulting metal laminate may be used to fabricate a variety of parts such as aerosol valv mounting cups, aerosol can domes, aerosol can bottoms, paint cans, metal pans or trays, and the like. Fig. 4 illustrates an aerosol valve mounting cup 20 formed by stamping the metal laminate formed from the protective film of the present invention. The compressible layer 12 allows the film to be readily compressed for fabricating such parts, and also provides a good seal, such as during crimping operations when the aerosol valve mounting cup is later crimped to a can body.
It should also be appreciated that the protective film may be laminated to both sides of a metal substrate. For example, the film thickness may be from 5-10 mils (0.13 mm - 0.25 mm) on the inside of an aerosol valve mounting cup, forming a sealing gasket, and from 1 -2 mils (0.025 mm - 0.05 mm) on the outside of the cup, forming a scratch resistant, corrosion resistant coating.
In order that the invention may be more readily understood, reference is made to the followin examples, which are intended to be illustrative of the invention, but are not intended to be limiting in scope.
Example 1
A three-layer protective polymeric film was produced in accordance with the present invention on a conventional cast film line. The scratch-resistant layer, which comprised 25 percent of the total film thickness, was comprised of a polypropylene homopolymer (Himont ProFaxTM PD-064). The compressible layer comprised 60 percent of the total film thickness and was comprised of a blend of 50 percent polypropylene (Himont ProFaxTM PD-064) and 50 percent ultra low density polyethylene (Dow Chemical ATTANE® 4201). The adhesive layer comprised 15 percent of the total film thickness and was comprised of a blend of 60 percent Quantum Chemical PlexarTM 360 maleic anhydride modified linear low density polyethylene and 40 percent Quantum Chemical PlexarTM 206 maleic anhydride modified high density polyethylene. Each layer was extruded at temperatures of 400-410°F (204-210°C) with a die temperature of 410°F (210°C). The coextruded film was quenched on a 100°F (38°C) casting roll and then wound into a roll. The resulting 8.0 mil (0.2 mm) thick film was then thermally laminated to a 10.5 mil (0.27 mm) tin-plated steel at 350°F (177°C) using a hot roll laminator. The film exhibited peel adhesion greater than 10.0 pounds per linear inch (1.8 kg/cm) when subjected to 180 degree peel testing using an Instron tensile tester (ASTM D-903). The resulting laminate was successfully stamped into aerosol valve mounting cups on a multistation progressive die. The film maintained excellent adhesion to the formed mounting cup.
Example 2
A three-layer 8.0 mil (0.2 mm) thick coextruded film was produced on conventional cast film line. The outermost scratch resistant layer, which was 25 percent of the total film gauge, was comprised of a polypropylene random copolymer (Himont Profax 7531). The compressible layer (60 percent of film gauge) was comprised of a blend of 50 percent polypropylene random copolymer (Himont Profax 7531) and 50 percent ultra low density polyethylene (Dow Chemical ATTANE 4202). The adhesive layer (15 percent of film gauge) was comprised of a blend of 60 percent Quantum
Chemical Plexar 360 maleic anhydride modified linear low density polyethylene and 40 percent Quantum Chemical Plexar 206 maleic anhydride modified high density polyethylene. Each layer was extruded at temperatures of 400-410°F (204-210°C) with a die temperature of 410°F (210°C). The film was quenched on a 100°F (38°C) casting roll and then wound into a roll. The 8.0 mil (0.2 mm) film was then thermally laminated to 10.5 mil (0.27 mm) tin plated steel at 350°F (177°C) using a hot roll laminator. The resulting laminate was successfully stamped into aerosol valve mounting cups on a multistation progressive die.
Example 3
Another 8.0 mil (0.2 mm) three-layer protective polymeric film was prepared as in Example 1. The scratch-resistant layer comprised 25 percent of the total film thickness and was comprised of a
polypropylene homopolymer (Himont ProFaxTM PD-064). The compressible layer comprised 60 percent of the total film thickness and was comprised of a very low density metallocene catalyst ethylene copolymer (Dow AFFINITY® PL-1840). The adhesive layer comprised 15 percent of the total film thickness and was comprised of 100 percent Quantum Chemical PlexarTM 360 maleic 5 anhydride modified linear low density polyethylene. Eachlayer was coextruded as described in
Example 1 , and the resulting film was quenched and thermally laminated to a 10.5 mil (0.27 mm) tin- plated steel.
Example 4
A three-layer protective polymeric film was prepared as in Example 1. The scratch-resistant l o layer (25 percent of total film thickness) was comprised of a polypropylene homopolymer (Himont ProFaxTM PD-064). The compressible layer (60 percent of total film thickness) was comprised of a blend of 50 percent polypropylene (Himont ProFaxTM PD-191) and 50 percent ultra low density polyethylene (Dow Chemical ATTANE® 4201) with a 1.5 phr of a sodium bicarbonate-citric acid based foam concentrate (Henley HydrocerolTM CF-20). The endothermic blowing agent was 15 activated during extrusion to produce a very fine closed cell foam compressible layer. The adhesive layer (15 percent of total film thickness) was comprised of 100 percent Quantum Chemical PlexarTM 360 maleic anhydride modified linear low density polyethylene. Each layer was extruded as described in Example 1 , and the resulting film was quenched and thermally laminated to a 10.5 mil (0.27 mm) tin-plated steel.
20 Example 5
A three-layer protective polymeric film was prepared as in Example 1 comprising a scratch- resistant layer (25 percent of total film thickness) of a polypropylene homopolymer (Himont ProFaxTM PD-064), a compressible layer (60 percent of total film thickness) comprising a blend of 65 percent polypropylene (Himont ProFaxTM PD-064) and 35 percent ethylene-propylene rubber (Exxon 25 Chemical VistalonTM 3708P). The adhesive layer was comprised of 100 percent Quantum Chemical PlexarTM 360 maleic anhydride modified linear low density polyethylene. Each layer was extruded as in Example 1, and the resulting film was quenched and thermally laminated to tin-plated steel.
Example 6
A two-layer 8.0 mil (0.2 mm) thick polymer film was produced on a conventional cast film line.
3 o The scratch-resistant layer comprised 80 percent of the total film thickness and was comprised of a 50 percent polypropylene (ProFaxTM PD-064) and 50 percent ultra low density polyethylene blend (ATTANE® 4201). The adhesive layer comprised 20 percent of the total film thickness and was comprised of a blend of 60 percent PlexarTM 360 linear low density polyethylene and 40 percent PlexarTM 206 high density polyethylene. The resulting film was thermally laminated to tin-plated steel
35 and stamped into an aerosol valve mounting cup as described in Example 1.
Example 7
Polypropylene, polyethylene, Plexar adhesives and blends, including those described in Examples 1-5, were hot pressed into 0.125 inch (0.32 cm) plaques using a heated platen press. The polymer plaques were then tested for durometer hardness using a Pacific Transducer Corp. Model 409 type D durometer tester according to ASTM D2240. The results are shown in Table I:
Example 8
A pencil hardness test (ASTM D-3363) was used to determine scratch resistance of the plaques in Example 7. A set of Eberhard Faber Design Drawing 3800 pencils with various lead hardnesses ranging from 6H (hard) to 6B (soft) were used to quantify hardness or scratch resistance of the various polymer blends given in Example 7. The results are shown below in Table II.
As can be seen, the plaques containing polypropylene or blends of polypropylene and ultra low density polyethylene exhibit the highest scratch resistance.
Example 9
In order to compare the relative abuse resistance of a film laminate with a 100 percent polypropylene protective layer with that of a film laminate with a protective layer comprised of 50 percent polypropylene and 50 percent ultra linear low density polyethylene, aerosol valve mounting cups produced from the laminates described in Example 1 and Example 6, respectively, were subjected to a vibratory shaker evaluation. Five aerosol valve mounting cups of each sample were placed into empty glass 9 oz. bottles which were mounted on a Lab-Line Instruments Multi-Wrist Shaker. The five identical metal laminate mounting cups in each of the bottles were subjected to vigorous shaking at an instrument setting of 10 (maximum) for five minutes. Cups were then removed and inspected for damage in the form of nicks, scratches or abrasion on the film laminate side using a 10X optical magnifying lupe. The cups of Example 6 (50 percent polypropylene - 50 percent ultra low density polyethylene top layer) exhibited an average of 22 surface damaging nicks on the laminate, while the cups of Example 1 (100 percent polypropylene top layer) exhibited an average of only 9 surface damaging nicks.
While certain representative embodiments and details have been shown for purposes of illustrating the invention, it will be apparent to those skilled in the art that various changes in the methods and apparatus disclosed herein may be made without departing from the scope of the invention, which is defined in the appended claims.
Claims
1. A protective film, comprising: a) a scratch-resistant layer, said scratch-resistant layer exhibiting a Shore D durometer hardness of at least 60 as tested according to ASTM D2240, said scratch-resistant layer comprising from 5 percent to 40 percent of the total protective film thickness; b) a compressible layer adjacent to said scratch-resistant layer, said compressible layer comprising homopolymers of ethylene or propylene, copolymers of ethylene and propylene, ethylene-propylene rubbers, elastomeric olefinic resins, styrene block copolymers, polyurethane, or blends thereof, said compressible layer comprising from 40 percent to 80 percent of the total protective film thickness; and c) an adhesive layer adjacent to said compressible layer, said adhesive layer comprising ethylenically unsaturated copolymers of vinyl acetate, ethyl acrylate, ethyl methacrylate, methyl acrylic acid, acrylic acid, or carbon monoxide; homopolymers of ethylene or propylene; copolymers of ethylene and propylene; ionomers of ethylene and methacrylic acid or acrylic acid; 5 maleic anhydride modified polyethylene; polyamides; polyurethanes; or compatible blends thereof, said adhesive layer comprising from 5 percent to 25 percent of the total protective film thickness, and said adhesive layer capable of exhibiting at least 5.0 pounds per linear inch (0.89 kg/cm) peel adhesion to metal substrates when subjected to a 180 degree peel test in accordance with ASTM D903, 0 wherein the total protective film thickness is from 0.5 to 20.0 mils ( 0.01 to 0.51 mm) thick.
2. A film according to Claim 1 , wherein the scratch-resistant layer comprises greater that 80 percent polypropylene.
3. A film according to Claim 1 , wherein the compressible layer consists essentially of a blend of polypropylene and polyethylene. 5 5. A film according to Claim 1 , wherein the adhesive layer consists essentially of a blen of maleic anhydride modified polyethylenes.
6. A metal laminate comprising a protective polymeric film bonded to at least one major surface of a metal substrate, said polymeric film comprising an adhesive layer comprising from 5 to 25 percent of the total film thickness, a compressible layer comprising from 40-80 percent of the total o film thickness, a scratch-resistant layer comprising from 5 to 40 percent of the total film thickness, said scratch-resistant layer having a Shore D hardness of at least 60, and said adhesive and compressible layers having a Shore D hardness of less than said scratch-resistant layer.
7. A metal laminate according to Claim 6, wherein said adhesive layer is selected from the group consisting of ethylenically unsaturated copolymers of vinyl acetate, ethyl acrylate, ethyl 5 methacrylate, methyl acrylic acid, acrylic acid, or carbon monoxide; homopolymers of ethylene or propylene; copolymers of ethylene and propylene; ionomers of ethylene and methacrylic acid or
acrylic acid; maleic anhydride modified polyethylene; polyamides; polyurethanes; or compatible blends thereof."
8. A metal laminate according to Claim 6, wherein said scratch-resistant layer is selected from the group consisting of polypropylene, polyethylene, polyester, polyamide, and blends thereof.
9. A metal laminate according to Claim 6, wherein said compressible layer comprises homopolymers of ethylene or propylene, copolymers of ethylene and propylene, ethylene-propylene rubbers, olefinic resins, styrene block copolymers, polyurethane, and blends thereof.
10. A metal laminate according to Claim 6, wherein said compressible layer is foamed. 11. A metal laminate according to Claim 6, wherein said scratch-resistant layer includes a curable coating selected from the group consisting of urethane, epoxy, acrylic and silicone.
12. A metal laminate according to Claim 6, wherein said scratch-resistant layer contains an inorganic filler.
13. A metal laminate according to Claim 6, wherein said scratch-resistant layer has been crosslinked.
14. An aerosol valve mounting cup formed from a protective polymeric film laminated to metal, said protective film comprising an adhesive layer comprising from 5 to 25 percent of the total film thickness, a compressible layer comprising from 40-80 percent of the total film thickness, and a scratch-resistant layer comprising from 5 to 40 percent of the total film thickness, said scratch- resistant layer having a Shore D hardness of at least 60, and said adhesive and compressible layers having a Shore D hardness of less than said scratch-resistant layer.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US38999895A | 1995-02-17 | 1995-02-17 | |
| US389998 | 1995-02-17 | ||
| PCT/US1996/001864 WO1996025292A1 (en) | 1995-02-17 | 1996-02-14 | Protective polymeric film for lamination to metal |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP0809572A1 true EP0809572A1 (en) | 1997-12-03 |
Family
ID=23540618
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP96906379A Withdrawn EP0809572A1 (en) | 1995-02-17 | 1996-02-14 | Protective polymeric film for lamination to metal |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP0809572A1 (en) |
| JP (1) | JPH11500077A (en) |
| KR (1) | KR19980702218A (en) |
| CA (1) | CA2212160A1 (en) |
| WO (1) | WO1996025292A1 (en) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19923780A1 (en) * | 1999-05-22 | 2000-11-23 | Beiersdorf Ag | Self adhesive film useful for protection of painted automobile surfaces during assembly and transport, comprises support layer of polypropylene block copolymer and adhesive film |
| EP1146100B1 (en) * | 2000-03-30 | 2004-08-04 | Atofina | Package being non-delaminable to a metal substrat and peelable to polypropylene |
| US6541568B1 (en) | 2000-06-01 | 2003-04-01 | Solvay Engineered Polymers | Polyolefin materials having enhanced surface durability |
| US6387508B1 (en) * | 2000-09-14 | 2002-05-14 | 3M Innovative Properties Company | Metal bonding film compositions |
| US6713166B2 (en) | 2000-09-28 | 2004-03-30 | Gunze Co., Ltd. | Laminating film and laminate |
| WO2002045957A1 (en) | 2000-12-06 | 2002-06-13 | Dow Global Technologies Inc. | Protective coating for metal surfaces containing a non-oriented multilayer film with a polyolefin core |
| DE102005055297A1 (en) * | 2005-11-21 | 2007-05-31 | Hühoco Metalloberflächenveredelung Gmbh | Metal-plastic composite body |
| WO2007133383A1 (en) * | 2006-05-09 | 2007-11-22 | Dow Global Technologies Inc. | Multilayer adhesive polymer film |
| KR101103901B1 (en) * | 2009-12-07 | 2012-01-12 | 삼화왕관주식회사 | Vacuum bottle cap and manufacturing method thereof |
| DE102015107032A1 (en) | 2015-05-06 | 2016-11-10 | Ccl Design Gmbh | Method for producing a stamped component |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60166455A (en) * | 1983-12-29 | 1985-08-29 | 住友化学工業株式会社 | polypropylene laminated film |
| AU613417B2 (en) * | 1987-12-01 | 1991-08-01 | Minnesota Mining And Manufacturing Company | High integrity composites |
| US5006383A (en) * | 1989-06-28 | 1991-04-09 | The Dow Chemical Company | Polymeric blend and laminated structures prepared therefrom |
| CA2007748C (en) * | 1989-08-31 | 1996-01-02 | Eiji Tamura | Food packaging container |
-
1996
- 1996-02-14 KR KR1019970705613A patent/KR19980702218A/en not_active Withdrawn
- 1996-02-14 EP EP96906379A patent/EP0809572A1/en not_active Withdrawn
- 1996-02-14 WO PCT/US1996/001864 patent/WO1996025292A1/en not_active Application Discontinuation
- 1996-02-14 JP JP8525054A patent/JPH11500077A/en active Pending
- 1996-02-14 CA CA002212160A patent/CA2212160A1/en not_active Abandoned
Non-Patent Citations (1)
| Title |
|---|
| See references of WO9625292A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| WO1996025292A1 (en) | 1996-08-22 |
| MX9706268A (en) | 1997-11-29 |
| JPH11500077A (en) | 1999-01-06 |
| KR19980702218A (en) | 1998-07-15 |
| CA2212160A1 (en) | 1996-08-22 |
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