US20170298240A1 - Solvent-uv hybrid inkjet ink for aluminum beverage can decoration - Google Patents
Solvent-uv hybrid inkjet ink for aluminum beverage can decoration Download PDFInfo
- Publication number
- US20170298240A1 US20170298240A1 US15/229,557 US201615229557A US2017298240A1 US 20170298240 A1 US20170298240 A1 US 20170298240A1 US 201615229557 A US201615229557 A US 201615229557A US 2017298240 A1 US2017298240 A1 US 2017298240A1
- Authority
- US
- United States
- Prior art keywords
- inkjet ink
- radiation
- ink
- hybrid
- curable
- 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.)
- Abandoned
Links
- 229910052782 aluminium Inorganic materials 0.000 title claims abstract description 23
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims abstract description 23
- 238000005034 decoration Methods 0.000 title claims abstract description 15
- 235000013361 beverage Nutrition 0.000 title claims description 13
- 239000000463 material Substances 0.000 claims abstract description 23
- 150000002118 epoxides Chemical class 0.000 claims abstract description 18
- 239000000758 substrate Substances 0.000 claims abstract description 16
- 239000003960 organic solvent Substances 0.000 claims abstract description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 9
- 239000000178 monomer Substances 0.000 claims description 31
- 239000002904 solvent Substances 0.000 claims description 23
- -1 glycol ethers Chemical class 0.000 claims description 22
- 238000000576 coating method Methods 0.000 claims description 21
- 239000002966 varnish Substances 0.000 claims description 20
- 238000000034 method Methods 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 14
- 239000011248 coating agent Substances 0.000 claims description 12
- 239000002270 dispersing agent Substances 0.000 claims description 12
- 239000003086 colorant Substances 0.000 claims description 10
- 239000011347 resin Substances 0.000 claims description 9
- 229920005989 resin Polymers 0.000 claims description 9
- 239000004593 Epoxy Substances 0.000 claims description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 7
- 239000000049 pigment Substances 0.000 claims description 7
- 125000001931 aliphatic group Chemical group 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 6
- 229920002635 polyurethane Polymers 0.000 claims description 5
- 239000004814 polyurethane Substances 0.000 claims description 5
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 150000002596 lactones Chemical class 0.000 claims description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 4
- 229920000728 polyester Polymers 0.000 claims description 4
- LAIJAUHBAWLPCO-UHFFFAOYSA-N (4-tert-butylcyclohexyl) prop-2-enoate Chemical compound CC(C)(C)C1CCC(OC(=O)C=C)CC1 LAIJAUHBAWLPCO-UHFFFAOYSA-N 0.000 claims description 3
- KUAUJXBLDYVELT-UHFFFAOYSA-N 2-[[2,2-dimethyl-3-(oxiran-2-ylmethoxy)propoxy]methyl]oxirane Chemical compound C1OC1COCC(C)(C)COCC1CO1 KUAUJXBLDYVELT-UHFFFAOYSA-N 0.000 claims description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 3
- PSGCQDPCAWOCSH-UHFFFAOYSA-N (4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl) prop-2-enoate Chemical group C1CC2(C)C(OC(=O)C=C)CC1C2(C)C PSGCQDPCAWOCSH-UHFFFAOYSA-N 0.000 claims description 2
- VOBUAPTXJKMNCT-UHFFFAOYSA-N 1-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound CCCCCC(OC(=O)C=C)OC(=O)C=C VOBUAPTXJKMNCT-UHFFFAOYSA-N 0.000 claims description 2
- BXGYYDRIMBPOMN-UHFFFAOYSA-N 2-(hydroxymethoxy)ethoxymethanol Chemical compound OCOCCOCO BXGYYDRIMBPOMN-UHFFFAOYSA-N 0.000 claims description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 2
- 125000004386 diacrylate group Chemical group 0.000 claims description 2
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 claims description 2
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 claims description 2
- 150000002334 glycols Chemical class 0.000 claims description 2
- 229920005862 polyol Polymers 0.000 claims description 2
- 150000003077 polyols Chemical class 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- 239000008365 aqueous carrier Substances 0.000 claims 1
- 230000001678 irradiating effect Effects 0.000 claims 1
- 239000000976 ink Substances 0.000 description 62
- 239000002253 acid Substances 0.000 description 12
- 239000000126 substance Substances 0.000 description 10
- 239000010408 film Substances 0.000 description 9
- 230000008569 process Effects 0.000 description 9
- 230000035882 stress Effects 0.000 description 8
- 150000002148 esters Chemical class 0.000 description 7
- 238000007639 printing Methods 0.000 description 7
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 6
- 238000007641 inkjet printing Methods 0.000 description 6
- 238000009928 pasteurization Methods 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 230000008901 benefit Effects 0.000 description 4
- 238000001723 curing Methods 0.000 description 4
- 238000011068 loading method Methods 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000003607 modifier Substances 0.000 description 4
- 238000007645 offset printing Methods 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- 239000004971 Cross linker Substances 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 229920000058 polyacrylate Polymers 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- NVVZQXQBYZPMLJ-UHFFFAOYSA-N formaldehyde;naphthalene-1-sulfonic acid Chemical class O=C.C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 NVVZQXQBYZPMLJ-UHFFFAOYSA-N 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- UPHWVVKYDQHTCF-UHFFFAOYSA-N octadecylazanium;acetate Chemical compound CC(O)=O.CCCCCCCCCCCCCCCCCCN UPHWVVKYDQHTCF-UHFFFAOYSA-N 0.000 description 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229920001281 polyalkylene Polymers 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000000935 solvent evaporation Methods 0.000 description 2
- 238000007655 standard test method Methods 0.000 description 2
- 230000008646 thermal stress Effects 0.000 description 2
- 239000012855 volatile organic compound Substances 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- RZVINYQDSSQUKO-UHFFFAOYSA-N 2-phenoxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC1=CC=CC=C1 RZVINYQDSSQUKO-UHFFFAOYSA-N 0.000 description 1
- 239000012958 Amine synergist Substances 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 238000010546 Norrish type I reaction Methods 0.000 description 1
- 238000010547 Norrish type II reaction Methods 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 229920006243 acrylic copolymer Polymers 0.000 description 1
- 239000002318 adhesion promoter Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000001311 chemical methods and process Methods 0.000 description 1
- 229950007046 chlorphentermine Drugs 0.000 description 1
- IPHJYJHJDIGARM-UHFFFAOYSA-M copper phthalocyaninesulfonic acid, dioctadecyldimethylammonium salt Chemical compound [Cu+2].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC.C=1C(S(=O)(=O)[O-])=CC=C(C(=NC2=NC(C3=CC=CC=C32)=N2)[N-]3)C=1C3=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 IPHJYJHJDIGARM-UHFFFAOYSA-M 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 238000002161 passivation Methods 0.000 description 1
- 238000009304 pastoral farming Methods 0.000 description 1
- 230000037361 pathway Effects 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000003504 photosensitizing agent Substances 0.000 description 1
- FSDNTQSJGHSJBG-UHFFFAOYSA-N piperidine-4-carbonitrile Chemical group N#CC1CCNCC1 FSDNTQSJGHSJBG-UHFFFAOYSA-N 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 238000003847 radiation curing Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000007142 ring opening reaction Methods 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- BTURAGWYSMTVOW-UHFFFAOYSA-M sodium dodecanoate Chemical compound [Na+].CCCCCCCCCCCC([O-])=O BTURAGWYSMTVOW-UHFFFAOYSA-M 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 229940082004 sodium laurate Drugs 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000001029 thermal curing Methods 0.000 description 1
- 239000003017 thermal stabilizer Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING 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
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/10—Printing inks based on artificial resins
- C09D11/101—Inks specially adapted for printing processes involving curing by wave energy or particle radiation, e.g. with UV-curing following the printing
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41J—TYPEWRITERS; SELECTIVE PRINTING MECHANISMS, i.e. MECHANISMS PRINTING OTHERWISE THAN FROM A FORME; CORRECTION OF TYPOGRAPHICAL ERRORS
- B41J2/00—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed
- B41J2/005—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed characterised by bringing liquid or particles selectively into contact with a printing material
- B41J2/01—Ink jet
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41J—TYPEWRITERS; SELECTIVE PRINTING MECHANISMS, i.e. MECHANISMS PRINTING OTHERWISE THAN FROM A FORME; CORRECTION OF TYPOGRAPHICAL ERRORS
- B41J3/00—Typewriters or selective printing or marking mechanisms characterised by the purpose for which they are constructed
- B41J3/407—Typewriters or selective printing or marking mechanisms characterised by the purpose for which they are constructed for marking on special material
- B41J3/4073—Printing on three-dimensional objects not being in sheet or web form, e.g. spherical or cubic objects
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING 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
- C09D11/00—Inks
- C09D11/30—Inkjet printing inks
- C09D11/36—Inkjet printing inks based on non-aqueous solvents
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/0041—Digital printing on surfaces other than ordinary paper
- B41M5/0047—Digital printing on surfaces other than ordinary paper by ink-jet printing
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/0041—Digital printing on surfaces other than ordinary paper
- B41M5/0058—Digital printing on surfaces other than ordinary paper on metals and oxidised metal surfaces
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/0082—Digital printing on bodies of particular shapes
- B41M5/0088—Digital printing on bodies of particular shapes by ink-jet printing
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M7/00—After-treatment of prints, e.g. heating, irradiating, setting of the ink, protection of the printed stock
- B41M7/0081—After-treatment of prints, e.g. heating, irradiating, setting of the ink, protection of the printed stock using electromagnetic radiation or waves, e.g. ultraviolet radiation, electron beams
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M7/00—After-treatment of prints, e.g. heating, irradiating, setting of the ink, protection of the printed stock
- B41M7/009—After-treatment of prints, e.g. heating, irradiating, setting of the ink, protection of the printed stock using thermal means, e.g. infrared radiation, heat
Definitions
- This invention pertains to solvent-UV hybrid inkjet inks adapted for use in inkjet decoration of aluminum beverage cans, to decorative and clear coatings produced with such inks, and to aluminum beverage cans decorated with images applied with such inks.
- Inkjet printing is widely used for digitally applying images to various substrates, which may be two-dimensional or three-dimensional. Such printing is achieved using inkjet printers having one or more printheads with nozzles for jetting the ink onto the substrate.
- the printheads are typically mounted on a carriage that moves back and forth as the substrate is advanced to receive the ink.
- the printheads can also be maintained in a stationary position and the substrate moved past the printheads.
- inkjet inks are formulated either with solvent carriers or with UV curable inks so that they can dry or cure, respectively, by solvent evaporation or UV radiation curing.
- solvent-based inkjet inks can accept high pigment loadings and produce thinner, more flexible coatings than UV cured inks.
- UV-cured inkjet inks also have important advantages, including quick curing, low VOCs, and good chemical resistance.
- Solvent-based inkjet inks do have limitations. For example, they typically do not adhere well to nonporous substrates like metal. Also, the final cured solvent-based inkjet ink films typically do not have good solvent resistance.
- ink performance is assessed by successfully passing the following critical evaluation points: 1) image resolution and quality, 2) ink cohesion with an overprint varnish, and 3) ink adhesion to the aluminum can. This assessment occurs throughout the can-making process, before and after heat exposure (thermal stress), can necking (mechanical stress), and pasteurization (chemical stress).
- the two-piece metal decoration process is carried out by first printing images on the outside of the can followed by an immediate application of a coating on the surface of the entire can (first piece), which is cured by baking at temperatures of 180-215° C. for 3-5 minutes. After this, the can is run through another baking step to thermally cure an inside spray-coated epoxy film that forms a barrier between the aluminum and beverage to protect product integrity. The cans are then subjected to a necking process, which reduces the diameter of the top edge of the cylindrical can down to end specifications.
- the necked cans will also be subjected to chemical stress by pasteurization prior to beverage filling and lid closure (second piece of two piece can), where the cans are submersed in 1% detergent at about 80-95° C. for 10-15 minutes. Since coatings prepared using low viscosity inks have suffered when subjected to this pasteurization step, it is also very important to ensure that any alternative formulations are able to withstand the stress of this chemical process.
- acrylate-based UV curable ink One type of digital inkjet ink that has the potential to meet the above requirements is acrylate-based UV curable ink.
- This type of ink generally: a) has excellent weather- and light-fastness durability, b) can be formulated at a 100% solids level to produce good overall film hardness, and c) is highly chemically resistant when sufficiently crosslinked.
- jettable acrylate-based UV curable inks have not generally been adopted in the marketplace because: 1) they produce overly thick printed images that impede necking, and 2) adhesive and cohesive failures are often encountered after the pasteurization step.
- a solvent-based digital ink might be considered to address the film thickness issue. This type of ink is thermally cured by solvent evaporation, leaving behind about 12-30% solids, producing a much thinner film.
- solvent-based inks are also rejected in the marketplace due their poor weatherability, light-fastness, and chemical resistance, and their high VOC content.
- solvent-based digital inks produce poor image quality compared to UV curable inks in metal can decorating applications.
- Embodiments of the present invention provide unique advances in digital printing on aluminum beverage cans using inkjet technology. These unique embodiments successfully pass the critical evaluation points and maintain high image quality and performance under duress from thermal stress due to oven baking and curing, mechanical stress due to can necking, and chemical stress due to pasteurization, and thus comprise a very significant contribution to the art.
- Embodiments of the present invention overcome the drawbacks of both acrylate-based UV curable and solvent-based inks by providing jettable low viscosity inkjet inks comprising a unique hybrid of UV-curable and solvent-based inks. These embodiments have highly desirable properties and advantages including: a) excellent weather- and light-fastness durability, b) ability to form thin films that can be formulated to a range of desired thicknesses, and c) excellent chemical resistance.
- Another important characteristic of embodiments is the ability to control step-wise cure.
- the printed image is UV-irradiated first, the resulting semi-cured film becomes immobile (pinned), yet is still wet due to the presence of unevaporated solvent.
- an overprint varnish by, e.g., an industry conventional roller coating process, intermixing of ink materials with overprint varnish components is achieved.
- This new ink-varnish composite produces a strong cohesion layer between the ink and varnish after the final thermal curing.
- overprint varnishes can be used.
- the overprint varnish preferably will include a solvent which may be either aqueous or organic.
- strong adhesion of the ink-varnish composite to aluminum cans may be enhanced by adding to the hybrid ink a third component that contains an epoxide functional group.
- a third component that contains an epoxide functional group By adding an epoxide-containing component to the hybrid ink and exposing the ink to high temperatures, the strain energy of the epoxide cyclic three-membered ring is released.
- application of elevated temperatures during the heat phase of the curing process is believed to catalyze the ring to break it open and covalently bind the ink to the aluminum surface.
- Hybrid inkjet ink embodiments of the present invention include, as necessary ingredients, about 3-49% by weight organic solvent based on the total weight of the ink, about 3-80% by weight of a UV radiation-curable material and an appropriate photoinitiator based on the total weight of the ink, and about 1-30% by weight of an epoxide-containing material based on the total weight of the ink.
- the organic solvent must be water miscible and preferably is food grade for applications to beverage cans.
- the organic solvent may be chosen from the group comprising of carbonates, lactones, glycols, and glycol ethers. Among these, lactones are currently preferred.
- the miscibility of the organic solvent with water based on weight percent ratio of organic solvent to water should be between about 95:5 and 5:95, and preferably between about 40:60 and 60:40.
- the UV radiation curable material may be chosen from one or more of a monofunctional UV curable monomer, a difunctional UV curable monomer or a trifunctional UV curable monomer.
- the UV curable component can contain two or more of a monofunctional UV curable monomer, a difunctional UV curable monomer or a trifunctional UV curable monomer.
- a mixture of all three of a monofunctional UV curable monomer, a difunctional UV curable monomer and a trifunctional UV curable monomer may be used.
- the monofunctional UV curable monomer may be a cycloaliphatic acrylate.
- Preferred cycloaliphatic acrylates include isobornyl acrylate and a most preferred cycloaliphatic acrylate is 4-tert-butylcyclohexylacrylate.
- Difunctional UV curable monomers When a difunctional UV curable monomer is used, it will act as a crosslinker. Difunctional monomers improve the hardness and chemical resistance of the film, as well as accelerate the rate of polymerization. Difunctional UV curable monomers that can be used include aliphatic, cycloaliphatic, polyester, polyurethane, and ethylene/propylene glycol diacrylates. Hexanediol diacrylate is preferred in embodiments and a most preferred difunctional UV curable monomer is dipropylene glycol diacrylate.
- Trifunctional UV curable monomer When a trifunctional UV curable monomer is used, it will also act as a cross-linker.
- One particularly preferred trifunctional UV curable monomer is propoxylated(3) trimethylopropane triacrylate. Trifunctional monomers provide harder films and a faster curing response with lower UV dosages.
- the UV curable component may also contain a resin to act as an adhesion promoter and/or to improve the hardness of the final coating.
- the resin may be, for example, one or more of a polyol, an acrylated polyester, or an acrylated polyurethane.
- the resin may be UV-radiation curable or it may not be UV-radiation curable.
- the molecular weights of the resin preferably will be less than about 100,000 Daltons, and most preferably will be in the range of about 1000-50,000 Daltons.
- composition will also include epoxy functional modifiers and photoinitiators that act as polymerization initiators.
- the epoxide containing material will be a mono-, di-, or tri-functional epoxide chosen from the group comprising aliphatic, aromatic, saturated and unsaturated epoxides. Among these, aliphatic epoxides are currently preferred. As explained earlier, the epoxide containing material is believed to act as cross-linkers and to improve the adhesion to metal oxide surfaces, such as the aluminum oxide found in the surface of aluminum cans.
- the epoxy containing material may comprise mono- or di-epoxy containing monomers.
- Preferred epoxy functional modifiers include cyclohexyl dimethanol diglycidyl ether. A particularly preferred epoxy functional modifier is neopentyl glycol diglycidyl ether.
- the inkjet ink composition may be used as a colorant-free clear coating or varnish, in most applications it will include a colorant, which can be pretreated so that it is self-dispersing or it may include a colorant in the form of a pigment or dye in combination with a separate dispersant. In the latter case the colorant will be stabilized using appropriate dispersants that are compatible with the UV curable component, the epoxy functional modifier, and the solvent.
- One measure of compatibility is that the combined components in the ink must be stable at elevated temperatures, broadly from about 20-80° C. for four weeks, and preferably from about 20-60° C. for two weeks.
- a dispersant is preferably added not only to improve the dispersibility of the colorant (when needed) but also to improve the storage stability of the ink.
- examples of dispersants that can be used include hydroxyl group-containing carboxylate esters, salts of long-chain polyaminoamides and esters of high molecular weight acids, salts of high molecular weight polycarboxylic acids, salts of long-chain polyaminoamides and esters of polar acids, esters of high molecular weight unsaturated acids, high molecular weight copolymers, modified polyurethanes, modified polyacrylates, polyetherester-based anionic surfactants, salts of naphthalenesulfonic acid-formalin con-densation products, salts of aromatic sulfonic acid-formalin condensation products, polyoxyethylene alkylphosphate esters, polyoxyethylene nonylphenyl ether, and stearylamine acetate.
- suitable dispersants include “Anti-Terra-U (a polyaminoamide phosphate)”, “Anti-Terra-203/204 (salts of high molecular weight polycarboxylic acids)”, “Disperbyk- 101 (a phosphate salt of a polyaminoamide and an acid ester), 107 (a hydroxyl group-containing carboxylate ester), 110 and 111 (copolymers that contain acid groups), 130 (a polya-25 mide), 161,162, 163,164, 165, 166 and 170 (high molecular weight copolymers)”, “Bykumen (an ester of a high molecular weight unsaturated acid)”, “BYK-P104, P105 (high molecular weight unsaturated polycarboxylic acids”, “P104S, 240S (systems containing a high molecular weight unsaturated polycarboxylic acid and silicon)”, and “Lactimon (a combination of a long-chain amine, an unsaturated polycarboxylic acid
- Still other suitable dispersants include “Demol RN and N (sodium salts of naphthalene- sulfonic acid-formalin condensates), MS, C and SN-B (sodium salts of aromatic sulfonic acid-formalin condensates), and EP”, “Homogenol L-18 (a polycarboxylic acid type polymer)”, “Emalgen 920, 930, 931,935,950 and 985 (polyoxy- ethylene nonylphenyl ethers)”, and “Acetamine 24 (a coconut amine acetate) and 86 (stearylamine acetate)” (Kao Corporation) “Solsperse 5000 (a phthalocyanine ammonium salt system), 13940 (a polyes-teramine system), 17000 (a fatty acid amine system), and 24000” (Avecia Ltd.) “Nikol T106 (a polyoxyethylene sorbitan monooleate) and MYS-IEX (a
- the inkjet ink composition will also include conventional ingredients like colorants, photosensitizers, photosynergists, stabilizers and surfactants.
- surfactants examples include fluorosurfactants, anionic surfactants such as sodium dodecylbenzenesulfonate, sodium laurate, and ammonium salts of polyoxyethylene alkyl ether sulfate; and nonionic surfactants such as polyoxy-ethylene alkyl ethers, polyoxyethylene alkyl esters, polyoxy-25 ethylene sorbitan fatty acid esters, polyoxyethylene alkylphenyl ethers, polyoxyethylene alkylamines, and polyoxyethylene alkylamides.
- Other examples of surfactants that can be used include polyoxyalkylene polyalkylene amines and sorbitan esters.
- polyoxyalkylene polyalkylene polyamines examples include Discole N-503, N-506, N-509, N-512, N-515, N-518, and N-520. (Dainichiseika Coln and Chemicals Mfg. Co.)
- Printed decorations prepared using the inkjet composition of embodiments will have a film thickness of about 1 to 12 ⁇ m, preferably about 1-10 ⁇ m and most preferably about 1-8 ⁇ m. These ink thicknesses enable the coating to successfully withstand mechanical stress put on the can container by the necking machinery.
- the coatings, in their final cured state will have a pencil hardness between 3B to 9H, and preferably between 2B to 9H.
- an overprint varnish will be applied to coatings prepared using the inkjet printing compositions.
- Overprint varnishes are used to help protect ink coatings.
- the level of protection and enhanced image quality achieved by intermixing the overprint varnish and the hybrid ink embodiments is outstanding.
- processes to produce decorative coatings in accordance with embodiments will entail: A) application of the inkjet composition using an inkjet printer followed by UV irradiation to achieve a partial cure; B) application of the overprint coating and, C) final heating to produce full cure.
- the UV curable component is initially pinned by applying UV radiation to cure (polymerize) that component, leaving the unevaporated solvent of the hybrid ink in place and an interim coating in the form of a “semi-wet print”.
- the overprint coating is applied to the “semi-wet print” it intermixes with the water miscible solvent component before the final heating step. While heating times and temperatures may vary depending on system parameters, the heating following the initial application may be carried out in an oven, for example, at about 80-350° C. for about 1-40 minutes, and most preferably about 180-215° C. for about 3-5 minutes.
- the outstanding adhesion image quality, glossiness and other properties achieved may be obtained when the aluminum oxide passivation layer formed on the surface of the can container during the heating step reacts with the oxygen in the epoxide group of the epoxide-containing component to initiate reaction with other components in the ink composition.
- the Al 3 ⁇ ion species on the surface of the can is coordinated by the epoxide oxygen, catalyzing a ring-opening and reaction with other components of the ink.
- test specimens were successfully necked cans with inkjet-applied decoration and an overprint varnish top coat.
- An ASTM standard test method D3359-09 was used to measure and examine the adhesion of inkjet-applied hybrid ink.
- a hard metal straight edge was used to make straight cuts with a sharp razor blade to form intersecting 7 to 8 crosshatched cuts in selected areas of the body and neck of the cans.
- the tape applied was a 0.75′′ wide transparent Scotch® Brand Tape, Cat 600.
- An ASTM standard test method D523-08 was used to measure the specular gloss of nonmetallic specimens for glossmeter geometries of 20, 60, and 85° using two specimens: 1) a hybrid black ink prepared in accordance with embodiments of the invention and applied using an inkjet printer, and 2) a commercial black beverage can coating prepared using conventional offset printing.
- a black hybrid inkjet ink as follows was used:
- the 20° geometry is advantageous for comparing specimens having 60° gloss values higher than 70.
- the 60° geometry is used for inter-comparing most specimens and for determining when the 20° geometry may be more applicable.
- the 85° geometry is used for comparing specimens for sheen or near-grazing shininess; it is most frequently applied when specimens have 60° gloss values lower than 10.
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Abstract
A hybrid inkjet ink comprising a water miscible organic solvent, a UV radiation-curable material and appropriate photoinitiator, and an epoxide-containing material and printed decorations produced by applying the inkjet ink images to an aluminum substrate.
Description
- This invention pertains to solvent-UV hybrid inkjet inks adapted for use in inkjet decoration of aluminum beverage cans, to decorative and clear coatings produced with such inks, and to aluminum beverage cans decorated with images applied with such inks.
- Inkjet printing is widely used for digitally applying images to various substrates, which may be two-dimensional or three-dimensional. Such printing is achieved using inkjet printers having one or more printheads with nozzles for jetting the ink onto the substrate. The printheads are typically mounted on a carriage that moves back and forth as the substrate is advanced to receive the ink. The printheads can also be maintained in a stationary position and the substrate moved past the printheads.
- Currently, inkjet inks are formulated either with solvent carriers or with UV curable inks so that they can dry or cure, respectively, by solvent evaporation or UV radiation curing. Typically, solvent-based inkjet inks can accept high pigment loadings and produce thinner, more flexible coatings than UV cured inks. UV-cured inkjet inks, however, also have important advantages, including quick curing, low VOCs, and good chemical resistance.
- The high pigment loadings achievable with solvent-based inks are not typically achievable with UV curable inks because these inks are inherently more viscous than solvent-based inks. Loading these inks with the high pigment levels necessary to produce intense and vibrant colors may make them too difficult to jet. Therefore, when it is desirable or necessary to produce intense and vibrant colors in inkjet printing, solvent-based inkjet inks that tolerate high pigment loadings are typically used.
- Solvent-based inkjet inks, however, do have limitations. For example, they typically do not adhere well to nonporous substrates like metal. Also, the final cured solvent-based inkjet ink films typically do not have good solvent resistance.
- Finding an alternative to conventional printing on aluminum beverage cans that allows easy customization of decoration and eliminates the need for very large print runs is highly desirable. Conventional printing on aluminum beverage cans (e.g. offset printing) is cumbersome since a plate must be produced for each image and color, and so a run of at least a substantial number of printed-cans is required by can manufacturers to recoup the plate costs. Digital printing using inkjet technology has the potential to revolutionize the industry since it can vary the image and color on-demand, and has the ability do so for single cans or small print runs.
- Therefore it would be highly desirable to find a way to decorate aluminum beverage cans using digital inkjet printers in order to take advantage of the speed, accuracy, economy, and ready customization of digital inkjet printing. Because of challenges presented by current solvent-based or UV curable inkjet inks like those noted above, this is not generally practical.
- In the beverage can industry, ink performance is assessed by successfully passing the following critical evaluation points: 1) image resolution and quality, 2) ink cohesion with an overprint varnish, and 3) ink adhesion to the aluminum can. This assessment occurs throughout the can-making process, before and after heat exposure (thermal stress), can necking (mechanical stress), and pasteurization (chemical stress).
- Currently, the two-piece metal decoration process is carried out by first printing images on the outside of the can followed by an immediate application of a coating on the surface of the entire can (first piece), which is cured by baking at temperatures of 180-215° C. for 3-5 minutes. After this, the can is run through another baking step to thermally cure an inside spray-coated epoxy film that forms a barrier between the aluminum and beverage to protect product integrity. The cans are then subjected to a necking process, which reduces the diameter of the top edge of the cylindrical can down to end specifications.
- During the necking procedure, the decoration and coating on the outer surface of the can body is exposed to significant mechanical stress and friction. Therefore application of overly thick or non-uniform decorative coatings may lead to decoration and coating failures. Additionally, the necked cans will also be subjected to chemical stress by pasteurization prior to beverage filling and lid closure (second piece of two piece can), where the cans are submersed in 1% detergent at about 80-95° C. for 10-15 minutes. Since coatings prepared using low viscosity inks have suffered when subjected to this pasteurization step, it is also very important to ensure that any alternative formulations are able to withstand the stress of this chemical process.
- One type of digital inkjet ink that has the potential to meet the above requirements is acrylate-based UV curable ink. This type of ink generally: a) has excellent weather- and light-fastness durability, b) can be formulated at a 100% solids level to produce good overall film hardness, and c) is highly chemically resistant when sufficiently crosslinked. However, jettable acrylate-based UV curable inks have not generally been adopted in the marketplace because: 1) they produce overly thick printed images that impede necking, and 2) adhesive and cohesive failures are often encountered after the pasteurization step.
- A solvent-based digital ink might be considered to address the film thickness issue. This type of ink is thermally cured by solvent evaporation, leaving behind about 12-30% solids, producing a much thinner film. However, solvent-based inks are also rejected in the marketplace due their poor weatherability, light-fastness, and chemical resistance, and their high VOC content. As a result, solvent-based digital inks produce poor image quality compared to UV curable inks in metal can decorating applications.
- Embodiments of the present invention provide unique advances in digital printing on aluminum beverage cans using inkjet technology. These unique embodiments successfully pass the critical evaluation points and maintain high image quality and performance under duress from thermal stress due to oven baking and curing, mechanical stress due to can necking, and chemical stress due to pasteurization, and thus comprise a very significant contribution to the art.
- Embodiments of the present invention overcome the drawbacks of both acrylate-based UV curable and solvent-based inks by providing jettable low viscosity inkjet inks comprising a unique hybrid of UV-curable and solvent-based inks. These embodiments have highly desirable properties and advantages including: a) excellent weather- and light-fastness durability, b) ability to form thin films that can be formulated to a range of desired thicknesses, and c) excellent chemical resistance.
- Another important characteristic of embodiments is the ability to control step-wise cure. When the printed image is UV-irradiated first, the resulting semi-cured film becomes immobile (pinned), yet is still wet due to the presence of unevaporated solvent. By applying to this semi-wet image an overprint varnish (by, e.g., an industry conventional roller coating process), intermixing of ink materials with overprint varnish components is achieved. This new ink-varnish composite produces a strong cohesion layer between the ink and varnish after the final thermal curing. Commercially available overprint varnishes can be used. The overprint varnish preferably will include a solvent which may be either aqueous or organic.
- Finally, strong adhesion of the ink-varnish composite to aluminum cans may be enhanced by adding to the hybrid ink a third component that contains an epoxide functional group. By adding an epoxide-containing component to the hybrid ink and exposing the ink to high temperatures, the strain energy of the epoxide cyclic three-membered ring is released. At the molecular level, it is believed that application of elevated temperatures during the heat phase of the curing process is believed to catalyze the ring to break it open and covalently bind the ink to the aluminum surface.
- Hybrid inkjet ink embodiments of the present invention include, as necessary ingredients, about 3-49% by weight organic solvent based on the total weight of the ink, about 3-80% by weight of a UV radiation-curable material and an appropriate photoinitiator based on the total weight of the ink, and about 1-30% by weight of an epoxide-containing material based on the total weight of the ink. The organic solvent must be water miscible and preferably is food grade for applications to beverage cans. The organic solvent may be chosen from the group comprising of carbonates, lactones, glycols, and glycol ethers. Among these, lactones are currently preferred. The miscibility of the organic solvent with water based on weight percent ratio of organic solvent to water, should be between about 95:5 and 5:95, and preferably between about 40:60 and 60:40.
- The UV radiation curable material may be chosen from one or more of a monofunctional UV curable monomer, a difunctional UV curable monomer or a trifunctional UV curable monomer. Alternatively, the UV curable component can contain two or more of a monofunctional UV curable monomer, a difunctional UV curable monomer or a trifunctional UV curable monomer. Finally, a mixture of all three of a monofunctional UV curable monomer, a difunctional UV curable monomer and a trifunctional UV curable monomer may be used.
- In embodiments, the monofunctional UV curable monomer may be a cycloaliphatic acrylate. Preferred cycloaliphatic acrylates include isobornyl acrylate and a most preferred cycloaliphatic acrylate is 4-tert-butylcyclohexylacrylate.
- When a difunctional UV curable monomer is used, it will act as a crosslinker. Difunctional monomers improve the hardness and chemical resistance of the film, as well as accelerate the rate of polymerization. Difunctional UV curable monomers that can be used include aliphatic, cycloaliphatic, polyester, polyurethane, and ethylene/propylene glycol diacrylates. Hexanediol diacrylate is preferred in embodiments and a most preferred difunctional UV curable monomer is dipropylene glycol diacrylate.
- When a trifunctional UV curable monomer is used, it will also act as a cross-linker. One particularly preferred trifunctional UV curable monomer is propoxylated(3) trimethylopropane triacrylate. Trifunctional monomers provide harder films and a faster curing response with lower UV dosages.
- The UV curable component may also contain a resin to act as an adhesion promoter and/or to improve the hardness of the final coating. The resin may be, for example, one or more of a polyol, an acrylated polyester, or an acrylated polyurethane. The resin may be UV-radiation curable or it may not be UV-radiation curable. The molecular weights of the resin preferably will be less than about 100,000 Daltons, and most preferably will be in the range of about 1000-50,000 Daltons.
- The composition will also include epoxy functional modifiers and photoinitiators that act as polymerization initiators.
- The epoxide containing material will be a mono-, di-, or tri-functional epoxide chosen from the group comprising aliphatic, aromatic, saturated and unsaturated epoxides. Among these, aliphatic epoxides are currently preferred. As explained earlier, the epoxide containing material is believed to act as cross-linkers and to improve the adhesion to metal oxide surfaces, such as the aluminum oxide found in the surface of aluminum cans. The epoxy containing material may comprise mono- or di-epoxy containing monomers. Preferred epoxy functional modifiers include cyclohexyl dimethanol diglycidyl ether. A particularly preferred epoxy functional modifier is neopentyl glycol diglycidyl ether.
- While the inkjet ink composition may be used as a colorant-free clear coating or varnish, in most applications it will include a colorant, which can be pretreated so that it is self-dispersing or it may include a colorant in the form of a pigment or dye in combination with a separate dispersant. In the latter case the colorant will be stabilized using appropriate dispersants that are compatible with the UV curable component, the epoxy functional modifier, and the solvent. One measure of compatibility is that the combined components in the ink must be stable at elevated temperatures, broadly from about 20-80° C. for four weeks, and preferably from about 20-60° C. for two weeks.
- In embodiments of the invention, a dispersant is preferably added not only to improve the dispersibility of the colorant (when needed) but also to improve the storage stability of the ink. Examples of dispersants that can be used include hydroxyl group-containing carboxylate esters, salts of long-chain polyaminoamides and esters of high molecular weight acids, salts of high molecular weight polycarboxylic acids, salts of long-chain polyaminoamides and esters of polar acids, esters of high molecular weight unsaturated acids, high molecular weight copolymers, modified polyurethanes, modified polyacrylates, polyetherester-based anionic surfactants, salts of naphthalenesulfonic acid-formalin con-densation products, salts of aromatic sulfonic acid-formalin condensation products, polyoxyethylene alkylphosphate esters, polyoxyethylene nonylphenyl ether, and stearylamine acetate.
- Specific examples of suitable dispersants include “Anti-Terra-U (a polyaminoamide phosphate)”, “Anti-Terra-203/204 (salts of high molecular weight polycarboxylic acids)”, “Disperbyk- 101 (a phosphate salt ofa polyaminoamide and an acid ester), 107 (a hydroxyl group-containing carboxylate ester), 110 and 111 (copolymers that contain acid groups), 130 (a polya-25 mide), 161,162, 163,164, 165, 166 and 170 (high molecular weight copolymers)”, “Bykumen (an ester of a high molecular weight unsaturated acid)”, “BYK-P104, P105 (high molecular weight unsaturated polycarboxylic acids”, “P104S, 240S (systems containing a high molecular weight unsaturated polycarboxylic acid and silicon)”, and “Lactimon (a combination of a long-chain amine, an unsaturated polycarboxylic acid, and silicon)”. These products are available from BYK Chemie. Other suitable dispersants include “Efka 44, 46, 47, 48, 49, 54, 63, 64, 65, 66, 71,701, 764 and 766”, “Efka Polymer 100 (a modified polyacrylate), 150 (an aliphatic modified polymer), 400, 401,402,403,450, 451,452 and 453 (modified polyacrylates), and 745 (a copper phthalocyanine system)” (Efka Chemicals), include “Florene TG-710 (a urethane oligomer)”, “Flonone SH-290 and SP-1000”, and 40 “Polyflow No. 50E and No. 300 (acrylic copolymers)”; and products manufactured by Kusumoto Chemicals Ltd. include “Disparlon KS-860, 873 SN and 874 (high molecular weight dispersants), #2150 (an aliphatic polyvalent carboxylic acid), and #7004 (a polyether ester)” (Kyoeisha Chemical Co., Ltd.)
- Still other suitable dispersants include “Demol RN and N (sodium salts of naphthalene- sulfonic acid-formalin condensates), MS, C and SN-B (sodium salts of aromatic sulfonic acid-formalin condensates), and EP”, “Homogenol L-18 (a polycarboxylic acid type polymer)”, “Emalgen 920, 930, 931,935,950 and 985 (polyoxy- ethylene nonylphenyl ethers)”, and “Acetamine 24 (a coconut amine acetate) and 86 (stearylamine acetate)” (Kao Corporation) “Solsperse 5000 (a phthalocyanine ammonium salt system), 13940 (a polyes-teramine system), 17000 (a fatty acid amine system), and 24000” (Avecia Ltd.) “Nikol T106 (a polyoxyethylene sorbitan monooleate) and MYS-IEX (a polyoxyethylene monostearate), and Hexagline 4-0 (a hexaglyceryl tetraoleate)” (Nikko Chemicals Co., Ltd.) “Ajisper PB821 and PB822 (basic dispersants)”. The quantity of the dispersant within the ink preferably represents from 0.1 to 10% by weight of the total weight of the ink (Ajinomoto-Fine-Techno Co., Inc.).
- In embodiments the inkjet ink composition will also include conventional ingredients like colorants, photosensitizers, photosynergists, stabilizers and surfactants.
- Examples of surfactants that can be used include fluorosurfactants, anionic surfactants such as sodium dodecylbenzenesulfonate, sodium laurate, and ammonium salts of polyoxyethylene alkyl ether sulfate; and nonionic surfactants such as polyoxy-ethylene alkyl ethers, polyoxyethylene alkyl esters, polyoxy-25 ethylene sorbitan fatty acid esters, polyoxyethylene alkylphenyl ethers, polyoxyethylene alkylamines, and polyoxyethylene alkylamides. Other examples of surfactants that can be used include polyoxyalkylene polyalkylene amines and sorbitan esters. Examples of polyoxyalkylene polyalkylene polyamines, include Discole N-503, N-506, N-509, N-512, N-515, N-518, and N-520. (Dainichiseika Coln and Chemicals Mfg. Co.)
- Printed decorations prepared using the inkjet composition of embodiments (exclusive of overprint varnish) will have a film thickness of about 1 to 12 μm, preferably about 1-10 μm and most preferably about 1-8 μm. These ink thicknesses enable the coating to successfully withstand mechanical stress put on the can container by the necking machinery.
- The coatings, in their final cured state (printed decoration and overprint varnish) will have a pencil hardness between 3B to 9H, and preferably between 2B to 9H.
- In embodiments an overprint varnish will be applied to coatings prepared using the inkjet printing compositions. Overprint varnishes are used to help protect ink coatings. However, in embodiments herein, the level of protection and enhanced image quality achieved by intermixing the overprint varnish and the hybrid ink embodiments is outstanding.
- In further embodiments, processes to produce decorative coatings in accordance with embodiments will entail: A) application of the inkjet composition using an inkjet printer followed by UV irradiation to achieve a partial cure; B) application of the overprint coating and, C) final heating to produce full cure. As noted earlier, in this wet-on-wet embodiment the UV curable component is initially pinned by applying UV radiation to cure (polymerize) that component, leaving the unevaporated solvent of the hybrid ink in place and an interim coating in the form of a “semi-wet print”. When the overprint coating is applied to the “semi-wet print” it intermixes with the water miscible solvent component before the final heating step. While heating times and temperatures may vary depending on system parameters, the heating following the initial application may be carried out in an oven, for example, at about 80-350° C. for about 1-40 minutes, and most preferably about 180-215° C. for about 3-5 minutes.
- While the inventors do not intend to limit the invention to any theoretical mechanisms or pathways, it is believed that the outstanding adhesion image quality, glossiness and other properties achieved may be obtained when the aluminum oxide passivation layer formed on the surface of the can container during the heating step reacts with the oxygen in the epoxide group of the epoxide-containing component to initiate reaction with other components in the ink composition. Another non-limiting possible explanation may be that the Al3− ion species on the surface of the can is coordinated by the epoxide oxygen, catalyzing a ring-opening and reaction with other components of the ink.
- The following examples are presented for purposes of illustration and are not intended to be exhaustive or limiting of any embodiment of the invention.
- 1. Adhesion to Aluminum Substrate
- The test specimens were successfully necked cans with inkjet-applied decoration and an overprint varnish top coat. An ASTM standard test method D3359-09 was used to measure and examine the adhesion of inkjet-applied hybrid ink. A hard metal straight edge was used to make straight cuts with a sharp razor blade to form intersecting 7 to 8 crosshatched cuts in selected areas of the body and neck of the cans. The tape applied was a 0.75″ wide transparent Scotch® Brand Tape, Cat 600.
- The crosshatch adhesion tests on both the necked areas of the can specimens and on the bodies of the can specimens for CMYK image hybrid coatings did not show any adhesion failure and had outstanding adhesion ratings of 4B- 5B, before and after pasteurization.
- 2. Gloss Level
- An ASTM standard test method D523-08 was used to measure the specular gloss of nonmetallic specimens for glossmeter geometries of 20, 60, and 85° using two specimens: 1) a hybrid black ink prepared in accordance with embodiments of the invention and applied using an inkjet printer, and 2) a commercial black beverage can coating prepared using conventional offset printing. A black hybrid inkjet ink as follows was used:
-
Material Type Percent by Weight 4-tert-butylcyclohexyl acrylate (monomer) 13 2-phenoxyethyl acrylate (monomer) 4 Propoxylated (3) Trimethylopropane Triacrylate 6 (trifunctional monomer) Resin 12 Amine Synergist 8 Antioxidant and thermal stabilizer blend 1 Surfactant 1 Photoinitiator Norrish Type I 3.5 Photoinitiator Norrish Type II 3.5 Black Pigment Dispersion (colorant) 15 Gamma-butyrolactone (solvent) 20 Neopentyl glycol diglycidyl ether (epoxide) 13 100 - The 20° geometry is advantageous for comparing specimens having 60° gloss values higher than 70. The 60° geometry is used for inter-comparing most specimens and for determining when the 20° geometry may be more applicable. The 85° geometry is used for comparing specimens for sheen or near-grazing shininess; it is most frequently applied when specimens have 60° gloss values lower than 10.
- The following results were obtained:
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Gloss Level Commercial Hybrid Angle Black Black 20° 57.6 66.7 60° 87.4 89.9 85° 96.6 94.4 - This data demonstrates that the hybrid inkjet black ink coating can produce gloss levels commensurate with those achieved using conventional offset printing processes. In other words, the new hybrid ink is shown here to enable inkjet printing on aluminum cans to produce gloss levels commensurate with those achieved in conventional offset printing processes thereby delivering all of the benefits of inkjet printing to the can printing process.
Claims (26)
1. A hybrid inkjet ink comprising, in percent by weight based on the weight of the ink:
about 3-49% of a water miscible organic solvent;
about 3-80% by weight of a UV radiation-curable material and an appropriate photoinitiator; and
about 1-30% by weight of an epoxide-containing material.
2. The hybrid inkjet ink of claim 1 in which the water miscible organic solvent is chosen from the group consisting of carbonates, lactones, glycols and glycol ethers.
3. The hybrid inkjet ink of claim 1 in which the organic solvent is a lactone.
4. The hybrid inkjet ink of claim 1 in which the UV radiation-curable material is chosen from the group consisting of: a monofunctional UV radiation-curable monomer, a difunctional UV radiation-curable monomer, and a trifunctional UV radiation-curable monomer.
5. The hybrid inkjet ink of claim 4 including two or more of a monofunctional UV radiation-curable monomer, a difunctional UV radiation-curable monomer, and a trifunctional UV radiation-curable monomer.
6. The hybrid inkjet ink of claim 1 in which the UV radiation-curable material comprises all three of a monofunctional UV radiation-curable monomer, a difunctional UV radiation-curable monomer, and a trifunctional UV radiation-curable monomer.
7. The hybrid inkjet ink of claim 1 in which the UV radiation-curable material monomer is a cycloaliphatic acrylate.
8. The hybrid inkjet ink of claim 7 in which the cycloaliphatic acrylate is isobornyl acrylate and/or 4-tert-butylcyclohexylacrylate.
9. The hybrid inkjet ink of claim 1 in which the UV radiation-curable material is difunctional and is chosen from the group consisting of aliphatic, cycloaliphatic, polyester, polyurethane, and ethylene/propylene glycol diacrylates.
10. The hybrid inkjet ink of claim 9 in which the difunctional UV radiation-curable material is hexanediol diacrylate and/or diprophylene glycol diacrylate.
11. The hybrid inkjet ink of claim 1 in which the radiation-curable material is propoxylated(3)trimethylopropane triacrylate.
12. The hybrid inkjet ink of claim 1 including a resin.
13. The hybrid inkjet ink of claim 12 in which the molecular weight of the resin is less than about 100,000 Daltons.
14. The hybrid inkjet ink of claim 12 in which the molecular weight of the resin is in the range of about 1000-50,000 Daltons.
15. The hybrid inkjet ink of claim 12 in which the resin is chosen from the group consisting of polyols, acrylated polyesters, and acrylated polyurethanes.
16. The hybrid inkjet ink of claim 1 in which the epoxide-containing material is a mono-, di-, or tri-functional epoxide chosen from the group consisting of aliphatic, aromatic, saturated and unsaturated epoxides.
17. The hybrid inkjet ink of claim 1 in which the epoxy-containing material comprises cyclohexyl dimethanol diglycidyl ether and/or neopentyl glycol diglycidyl ether.
18. The hybrid inkjet ink of claim 1 including a colorant.
19. The hybrid inkjet ink of claim 18 in which the colorant is a pigment or dye in combination with a dispersant stabilized using dispersants that are compatible with the remaining components of the inkjet ink.
20. A printed decoration comprising:
an aluminum substrate; and
an ink composition applied to the aluminum substrate using an inkjet printer, where the inkjet composition comprises, based upon the total weight of the ink, about 3-49% by weight of a water miscible organic solvent, about 3-80% by weight of a UV radiation-curable material and an appropriate photoinitiator and about 1-30% by weight of an epoxide-containing material.
21. A method of producing a printed decoration to an aluminum substrate comprising:
providing an aluminum substrate;
providing an inkjet ink composition comprising, based on the total weight of the ink, about 3-49% by weight of water miscible organic solvent, about 3-80% by weight of a UV radiation-curable component, and an appropriate photoinitiator; and about 1-30% by weight of an epoxide-containing material;
applying the inkjet composition to the aluminum substrate using an inkjet printer to form an image on the substrate;
irradiating the image with UV light to achieve a partial cure of the UV curable component of the ink, pinning the image to the substrate while leaving unevaporated solvent in place within the image;
applying an overprint varnish coating to intermix with the unevaporated solvent in the image; and
heating the image to drive off the solvent and produce a full cure of the image as a decoration on the aluminum substrate.
22. The method of claim 21 in which the overprint varnish includes an aqueous carrier.
23. The method of claim 21 in which the overprint varnish includes an organic carrier.
24. The method of claim 21 in which the aluminum substrate is the outer surface of an aluminum beverage can.
25. The hybrid inkjet ink of claim 21 in which the printed decorations have a thickness exclusive of overprint varnish of about 1 to 12 μm.
26. The hybrid inkjet ink of claim 21 in which the printed decorations have a thickness exclusive of overprint varnish of about 1-8 μm.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US15/229,557 US20170298240A1 (en) | 2016-04-13 | 2016-08-05 | Solvent-uv hybrid inkjet ink for aluminum beverage can decoration |
| US16/402,036 US10961407B2 (en) | 2016-04-13 | 2019-05-02 | Solvent-UV hybrid inkjet ink for aluminum beverage can decoration |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662322007P | 2016-04-13 | 2016-04-13 | |
| US15/229,557 US20170298240A1 (en) | 2016-04-13 | 2016-08-05 | Solvent-uv hybrid inkjet ink for aluminum beverage can decoration |
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| US16/402,036 Continuation US10961407B2 (en) | 2016-04-13 | 2019-05-02 | Solvent-UV hybrid inkjet ink for aluminum beverage can decoration |
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| US20170298240A1 true US20170298240A1 (en) | 2017-10-19 |
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| US16/402,036 Active US10961407B2 (en) | 2016-04-13 | 2019-05-02 | Solvent-UV hybrid inkjet ink for aluminum beverage can decoration |
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| US16/402,036 Active US10961407B2 (en) | 2016-04-13 | 2019-05-02 | Solvent-UV hybrid inkjet ink for aluminum beverage can decoration |
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| US (2) | US20170298240A1 (en) |
| EP (1) | EP3426738B1 (en) |
| JP (1) | JP7049999B2 (en) |
| ES (1) | ES3035560T3 (en) |
| PL (1) | PL3426738T4 (en) |
| PT (1) | PT3426738T (en) |
| WO (1) | WO2017180637A1 (en) |
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| US20220305833A1 (en) * | 2019-05-01 | 2022-09-29 | Xerox Corporation | Apparatus and method for deposting an overcoat on an image on a substrate |
| JP2023124249A (en) * | 2022-02-25 | 2023-09-06 | アルテミラ製缶株式会社 | Painted aluminum container, method for producing painted aluminum container |
| JP2023124251A (en) * | 2022-02-25 | 2023-09-06 | アルテミラ製缶株式会社 | Painted aluminum container, method for producing painted aluminum container |
| US11884056B2 (en) * | 2016-12-08 | 2024-01-30 | Crown Packaging Technology, Inc. | Forming a texture in a can surface decoration |
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| US20200269623A1 (en) * | 2019-02-22 | 2020-08-27 | Xyrec Ip B.V. | Methods of printing on non-permeable surfaces |
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| JP7713861B2 (en) * | 2021-11-08 | 2025-07-28 | アルテミラ製缶株式会社 | Painted aluminum container and method for manufacturing painted aluminum container |
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Also Published As
| Publication number | Publication date |
|---|---|
| PT3426738T (en) | 2025-07-17 |
| JP2019518812A (en) | 2019-07-04 |
| US20200095436A1 (en) | 2020-03-26 |
| WO2017180637A1 (en) | 2017-10-19 |
| EP3426738A4 (en) | 2019-12-04 |
| PL3426738T4 (en) | 2025-10-20 |
| ES3035560T3 (en) | 2025-09-04 |
| EP3426738A1 (en) | 2019-01-16 |
| EP3426738B1 (en) | 2025-03-26 |
| JP7049999B2 (en) | 2022-04-07 |
| US10961407B2 (en) | 2021-03-30 |
| PL3426738T3 (en) | 2025-10-13 |
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