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WO2018042193A1 - Procédé d'impression - Google Patents

Procédé d'impression Download PDF

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Publication number
WO2018042193A1
WO2018042193A1 PCT/GB2017/052555 GB2017052555W WO2018042193A1 WO 2018042193 A1 WO2018042193 A1 WO 2018042193A1 GB 2017052555 W GB2017052555 W GB 2017052555W WO 2018042193 A1 WO2018042193 A1 WO 2018042193A1
Authority
WO
WIPO (PCT)
Prior art keywords
primer
ink
multifunctional
weight
present
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.)
Ceased
Application number
PCT/GB2017/052555
Other languages
English (en)
Inventor
Brian Woolrich
Sean Slater
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Fujifilm Speciality Ink Systems Ltd
Original Assignee
Fujifilm Speciality Ink Systems Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from GBGB1614966.8A external-priority patent/GB201614966D0/en
Priority claimed from GBGB1618379.0A external-priority patent/GB201618379D0/en
Application filed by Fujifilm Speciality Ink Systems Ltd filed Critical Fujifilm Speciality Ink Systems Ltd
Priority to GB1904606.9A priority Critical patent/GB2569072B/en
Publication of WO2018042193A1 publication Critical patent/WO2018042193A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

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
    • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
    • B41M5/0011—Pre-treatment or treatment during printing of the recording material, e.g. heating, irradiating
    • 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
    • B41M5/0011—Pre-treatment or treatment during printing of the recording material, e.g. heating, irradiating
    • B41M5/0017—Application of ink-fixing material, e.g. mordant, precipitating agent, on the substrate prior to printing, e.g. by ink-jet printing, coating or spraying
    • 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
    • B41M5/0064—Digital printing on surfaces other than ordinary paper on plastics, horn, rubber, or other organic polymers
    • 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
    • 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
    • C09D11/106—Printing inks based on artificial resins containing macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C09D11/107—Printing inks based on artificial resins containing macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds from unsaturated acids or derivatives thereof
    • 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

Definitions

  • This invention relates to a method of printing and in particular to a method of printing utilising inks that have high gloss and excellent colour gamut, and that provide hard cured films with solvent-resistant properties.
  • UV-curable digital inkjet inks that have high gloss and excellent colour gamut, and that provide hard cured films with solvent-resistant properties are known in the art.
  • These inks typically contain one or more multifunctional monomers and optionally one or more multifunctional oligomers, wherein the total weight of the multifunctional monomers combined with, when present, the multifunctional oligomers, is at least 15% by weight based on the total weight of the ink.
  • a minimum of 15% multifunctional monomers and optionally multifunctional oligomers is required to provide sufficient crosslinking in the printed ink film upon curing and hence hard cured films with solvent-resistant properties.
  • multifunctional monomers and multifunctional oligomers have the properties required to provide a printed ink film with a high gloss and excellent colour density. All of these properties result in a printed ink film with a highly desirable combination of excellent appearance and physical properties.
  • the present invention provides a method of inkjet printing comprising the following steps, in order: (i) providing a substrate; (ii) jetting a primer onto the substrate, wherein the primer comprises one or more monofunctional monomers, a passive resin and one or more photoinitiators, wherein the one or more monofunctional monomers are present in at least 85% by weight, based on the total weight of the primer; (iii) jetting an inkjet ink onto the primer, wherein the inkjet ink comprises one or more multifunctional monomers, a colourant, one or more photoinitiators and optionally one or more multifunctional oligomers, wherein the total weight of the multifunctional monomers combined with, when present, the multifunctional oligomers, is at least 15% by weight based on the total weight of the ink; and (iv) curing the primer and the inkjet ink.
  • the present invention further provides: a printed substrate obtainable by the method; a primer as defined in relation to the method; and an ink set comprising a primer as defined in relation to the method and an inkjet ink as defined in relation to the method.
  • a printed substrate obtainable by the method
  • a primer as defined in relation to the method
  • an ink set comprising a primer as defined in relation to the method and an inkjet ink as defined in relation to the method.
  • the method of printing of the present invention is a method of inkjet printing.
  • minute droplets of black, white or coloured ink are ejected in a controlled manner from one or more reservoirs or printing heads through narrow nozzles on to a substrate which is moving relative to the reservoirs.
  • the ejected ink forms an image on the substrate.
  • the inks must flow rapidly from the printing heads, and, to ensure that this happens, they must have, in use, a low viscosity, typically below 100 mPas at 25°C (although in most applications the viscosity should be below 50 mPas, and often below 25 mPas).
  • the ink when ejected through the nozzles, the ink has a viscosity of less than 25 mPas and preferably 5-15 mPas at the jetting temperature, which is often elevated to about 35 to 50°C (the ink might have a much higher viscosity at ambient temperature).
  • the inks must also be resistant to drying and curing in the reservoirs or nozzles.
  • the method of the present invention includes step (i), providing a substrate.
  • substrates are suitable for use in the method, including substrates that have previously been difficult to print onto using the inkjet ink that is used in the method. Suitable substrates include polycarbonate (PC), fluted polypropylene (FPP), polypropylene (PP), self-adhesive vinyl (SAV), acrylic and high impact polystyrene (HIPS).
  • the method of the present invention includes step (ii), jetting a primer onto the substrate, wherein the primer comprises one or more monofunctional monomers, a passive resin and one or more photoinitiators, wherein the one or more monofunctional monomers are present in at least 85% by weight, based on the total weight of the primer.
  • the primer of the present invention which is jetted in step (ii) of the method of the present invention, comprises one or more monofunctional monomers, a passive resin and one or more photoinitiators, wherein the one or more monofunctional monomers are present in at least 85% by weight, based on the total weight of the primer.
  • Such a primer may be prepared by known methods such as, for example, mixing with a high-speed stirrer. Further, the primer exhibits a desirable low viscosity, less than 100 mPas, preferably 50 mPas or less and most preferably 30 mPas or less at 25°C.
  • the primer preferably has a viscosity of 10 mPas or more at 25°C, more preferably greater than 15 mPas at 25°C.
  • the primer preferably has a viscosity of 10 mPas or more but 30 mPas or less at 25°C so that the viscosity of the primer is similar to the viscosity of the inkjet ink.
  • the viscosity of the primer matches the viscosity of the inkjet ink ⁇ 20%, more preferably the viscosity of the primer matches the viscosity of the inkjet ink ⁇ 10%.
  • the viscosity of the primer is adjusted by controlling the amount of passive resin that is present in the primer. Viscosity may be measured using a digital Brookfield viscometer fitted with a thermostatically controlled cup and spindle arrangement, such as model LDV1 +.
  • the primer of the present invention which is jetted in step (ii) of the method of the present invention, is a radiation-curable (often termed "UV") primer.
  • radiation-curable is meant a material that polymerises or crosslinks when exposed to actinic radiation, commonly ultraviolet light, in the presence of a photoinitiator.
  • the primer does not, therefore, require the presence of water or a volatile organic solvent to effect drying of the ink.
  • a radiation-curable primer is typically free of volatile organic solvent and water.
  • the primer comprises less than 5% by weight of volatile organic solvent and water combined, preferably less than 3% by weight combined, more preferably, less than 2% by weight combined and most preferably less than 1 % by weight combined, based on the total weight of the primer.
  • Some water will typically be absorbed by the primer from the air and solvents may be present as impurities in the components of the primer, but such low levels are tolerated.
  • the primer of the present invention which is jetted in step (ii) of the method of the present invention, contains one or more monofunctional monomers.
  • monofunctional is meant that the monomers have only one functional group which takes part in a polymerisation reaction during curing.
  • the one or more monofunctional monomers are present in at least 85% by weight, based on the total weight of the primer. In a preferred embodiment, the one or more monofunctional monomers are present in at least 90% by weight, based on the total weight of the primer. The one or more monofunctional monomers are preferably present in no more than 95% by weight, based on the total weight of the primer.
  • the monofunctional monomers in combination with the passive resin facilitate good adhesion between the substrate and the overlying inkjet ink. This means that the inkjet ink can now be printed onto substrates that were previously difficult to gain adherence to, such as polycarbonate, acrylic and polypropylene, and the final printed substrates can now be print finished.
  • the one or more monofunctional monomers are selected from monofunctional (meth)acrylate monomers, N-vinyl amides, N-(meth)acryloyl amines, ⁇ , ⁇ -unsaturated ether monomers and combinations thereof.
  • the one or more monofunctional monomers include monofunctional (meth)acrylate monomers.
  • Monofunctional (meth)acrylate monomers are esters of (meth)acrylic acid and are well known in the art.
  • the substituents of the monofunctional monomers are not limited other than by the constraints imposed by the use in primer, such as viscosity, stability, toxicity etc.
  • the substituents are typically alkyl, cycloalkyl, aryl and combinations thereof, any of which may be interrupted by heteroatoms.
  • Non-limiting examples of substituents commonly used in the art include CMS alkyl, C 3-18 cycloalkyl, C 6 _ 10 aryl and combinations thereof, such as C 6 .
  • aryl- or C 3-18 cycloalkyl-substituted CMS alkyl any of which may be interrupted by 1 -10 heteroatoms, such as oxygen or nitrogen, with nitrogen further substituted by any of the above described substituents.
  • the substituents may together also form a cyclic structure.
  • Examples include a monomer selected from phenoxyethyl acrylate (PEA), cyclic TMP formal acrylate (CTFA), isobornyl acrylate (IBOA), tetrahydrofurfuryl acrylate (THFA), dicyclopentenyl oxyethyl acrylate, octadecyl acrylate, trimethyl cyclohexyl acrylate (TMCHA), tertiobutyl cyclohexyl acrylate (TBCHA) or combinations thereof.
  • the primer of the invention can include one monofunctional (meth)acrylate monomer or a mixture of two or more monofunctional (meth)acrylate monomers. A mixture of two or more monofunctional (meth)acrylate monomers is particularly preferred.
  • the primer includes a cyclic monofunctional (meth)acrylate. That is, the radical covalently bonded to the (meth)acrylate unit is cyclic.
  • the cyclic radical may be saturated or unsaturated, including aromatic.
  • Preferred cyclic monofunctional (meth)acrylates for the primer are phenoxyethyl acrylate (PEA), cyclic TMP formal acrylate (CTFA), isobornyl acrylate (IBOA), tetrahydrofurfuryl acrylate (THFA) or mixtures thereof.
  • PETFA phenoxyethyl acrylate
  • CCA cyclic TMP formal acrylate
  • IBOA isobornyl acrylate
  • THFA tetrahydrofurfuryl acrylate
  • the monofunctional (meth)acrylates present are exclusively cyclic, i.e. they are the sole monofunctional (meth)acrylate(s) present.
  • a particularly preferred combination is a saturated and an unsaturated, particular aromatic, monofunctional (meth)acrylate monomer.
  • IBOA Isobornyl acrylate
  • THFA Tetrahydrofurfuryl acrylate
  • the one or more monofunctional monomers are monofunctional (meth)acrylate monomers.
  • the one or more monofunctional monomers are monofunctional (meth)acrylate monomers comprising PEA, IBOA, CTFA or mixtures thereof.
  • the preferred one or more monofunctional (meth)acrylate monomers have a good affinity for the overlying inkjet ink.
  • the one or more monofunctional monomers may include one or more N-vinyl amides, N- (meth)acryloyl amines, ⁇ , ⁇ -unsaturated ether monomers and combinations thereof.
  • N-Vinyl amides are well-known monomers in the art and a detailed description is therefore not required.
  • N-Vinyl amides have a vinyl group attached to the nitrogen atom of an amide which may be further substituted in an analogous manner to (meth)acrylate monomers.
  • Preferred examples include N-vinyl amides having an aliphatic or aromatic cyclic group. The cyclic group may optionally include one or more heteroatoms such as oxygen or nitrogen.
  • Preferred examples are N-vinyl caprolactam (NVC) and N-vinyl pyrrolidone (NVP). NVC is particularly preferred.
  • N-acryloyl amines are also well-known in the art.
  • N-Acryloyl amines also have a vinyl group attached to an amide but via the carbonyl carbon atom and again may be further substituted in an analogous manner to (meth)acrylate monomers.
  • Preferred examples include N-acryloyl amines having a cyclic group.
  • the cyclic group may optionally include one or more heteroatoms such as oxygen or nitrogen.
  • a preferred example is N-acryloylmorpholine (ACMO).
  • the one or more monofunctional monomers may also include ⁇ , ⁇ -unsaturated ether monomers, such as vinyl ethers. These monomers are known in the art and may be used to reduce the viscosity of the primer.
  • a typical vinyl ether monomer which may be used in the primer of the present invention is ethylene glycol monovinyl ether. Mixtures of vinyl ether monomers may be used.
  • the one or more monofunctional monomers each have a glass transition temperature (Tg) of more than -15°C, more preferably more than 0°C. The Tg may be measured by DSC with a heating ramp of 10°C/min. If the one or monofunctional monomers each have a glass transition temperature (Tg) of more than -15°C or more preferably more than 0°C, the cured films are harder and hence more durable.
  • the monofunctional monomers have a tendency to migrate into the overlying inkjet ink and the migration of any monofunctional monomers with a Tg of less than 0°C from the primer into the inkjet ink has an adverse effect on the hardness of the overlying printed inkjet ink film.
  • 2-(2-ethoxyethoxy)ethyl acrylate (EOEOEA) has a Tg of -70°C and as the amount of EOEOEA in the primer increases, the overlying printed inkjet ink film becomes softer.
  • the primer preferably comprises less than 20% by weight of THFA based on the total weight of the primer, more preferably less than 10% by weight of THFA based on the total weight of the primer and more preferably, the primer is substantially free from THFA.
  • the primer comprises 2% by weight or less of multifunctional monomers.
  • the inclusion of multifunctional monomers in the primer causes shrinkage and thus has an adverse effect on the adhesion between the substrate and the overlying inkjet ink.
  • 2% by weight or less of multifunctional monomers in the primer is tolerated and provides cohesion to the primer.
  • the multifunctional monomer which is limited in amount may be any multifunctional monomer which could be involved in the curing reaction, such as a multifunctional (meth)acrylate monomer or a multifunctional vinyl ether.
  • the multifunctional acrylate monomers whose level is minimised include hexanediol diacrylate, polyethylene glycol diacrylate (for example tetraethyleneglycol diacrylate), dipropylene glycol diacrylate, neopentylglycol diacrylate, 3-methyl pentanediol diacrylate, the acrylate esters of ethoxylated or propoxylated glycols and polyols, for example, propoxylated neopentyl glycol diacrylate, trimethylolpropane triacrylate, pentaerythritol triacrylate, tri(propylene glycol) triacrylate, bis(pentaerythritol) hexaacrylate, and the acrylate esters of ethoxy
  • multifunctional acrylate monomers include esters of methacrylic acid (i.e. methacrylates), such as hexanediol dimethacrylate, triethyleneglycol dimethacrylate, diethyleneglycol dimethacrylate, ethyleneglycol dimethacrylate, 1 ,4-butanediol dimethacrylate, trimethylolpropane trimeth acrylate and combinations thereof.
  • methacrylates esters of methacrylic acid (i.e. methacrylates), such as hexanediol dimethacrylate, triethyleneglycol dimethacrylate, diethyleneglycol dimethacrylate, ethyleneglycol dimethacrylate, 1 ,4-butanediol dimethacrylate, trimethylolpropane trimeth acrylate and combinations thereof.
  • CTFA may contain approximately 5% trimethylolpropane triacrylate (TMPTA), a multifunctional monomer, as a reaction by-product.
  • TMPTA trimethylolpropane triacrylate
  • the primer comprises 30% by weight or less of CTFA, based on the total weight of the primer.
  • (Meth)acrylate is intended herein to have its standard meaning, i.e. acrylate and/or methacrylate.
  • Mono and multifunctional are also intended to have their standard meanings, i.e. one and two or more groups, respectively, which take part in the polymerisation reaction on curing.
  • the primer does not contain a radiation-curable oligomer.
  • a radiation-curable oligomer has its standard meaning in the art, namely that the component is partially reacted to form a pre-polymer having a plurality of repeating monomer units, which is capable of further polymerisation.
  • the oligomer preferably has a weight-average molecular weight of at least 600 Da. The weight-average molecular weight is preferably below 3,000 Da.
  • Molecular weights can be calculated if the structure of the oligomer is known or molecular weights can be measured using gel permeation chromatography using polystyrene standards.
  • Radiation-curable oligomers comprise a backbone, for example a polyester, urethane, epoxy or polyether backbone, and one or more radiation-curable groups.
  • the polymerisable group can be any group that is capable of polymerising upon exposure to radiation.
  • the primer of the present invention which is jetted in step (ii) of the method of the present invention, contains a passive resin.
  • Passive resins are resins which do not enter into the curing process, i.e. the resin is free of functional groups which polymerise under the curing conditions to which the ink is exposed. In other words, the resin is not a radiation-curable material.
  • Any passive resin that is compatible with the other primer components is suitable for use in the primer as long as it is soluble in the one or more monofunctional monomers of the primer.
  • suitable passive resins include epoxy resin, a polyester resin, a vinyl resin, a ketone resin, an aldehyde resin, a nitrocellulose resin, a phenoxy resin, a polyolefin resin and combinations thereof.
  • Some of the multifunctional monomer of the inkjet ink that is jetted in step (iii) of the method of the present invention can migrate into the primer and cause shrinkage of the primer.
  • the passive resin of the primer acts as a spacer to separate the radiation-curable material present in the primer so that any shrinkage is distributed across the whole primer layer. In this way, adhesion is maintained. Further, the presence of the passive resin in the primer allows a small amount of multifunctional monomer in the primer to be tolerated.
  • the passive resin preferably has a weight-average molecular weight of 3,000 Da or above, as determined by gel permeation chromatography (GPC) with polystyrene standards.
  • the weight- average molecular weight is preferably below 200,000 Da.
  • the passive resin has a weight-average molecular weight of 15,000 to 60,000 Da.
  • the passive resin has a glass transition temperature (Tg) of 45 to 100°C. The Tg may be measured by DSC with a heating ramp of 10°C/min.
  • the passive resin is a (meth)acrylic copolymer such as a copolymer of methyl (meth)acrylate with butyl, isobutyl or isobornyl (meth)acrylate.
  • (Meth)acrylate copolymers may also contain styrene.
  • An example of a preferred passive resin is Dianal BR 1 13 from Dianal America, Inc., an acrylic copolymer with a weight-average molecular weight of 30 kDa and a Tg of 78°C.
  • the passive resin is present in 1 -10% by weight, more preferably 2-6% by weight, based on the total weight of the primer.
  • the amount of passive resin that is present in the primer is adjusted to achieve the desired viscosity of the primer.
  • the primer of the present invention which is jetted in step (ii) of the method of the present invention, contains one or more photoinitiators, which under irradiation, for example using ultraviolet light, initiate the polymerisation of the radiation-curable material.
  • photoinitiators are known and commercially available such as, for example, under the trade names Irgacure (from BASF), Darocur (from Ciba) and Lucirin (from BASF).
  • the primer of the present invention is preferably cured by ultraviolet irradiation.
  • the radiation-curable material polymerises by free-radical polymerisation.
  • the photoinitiator is present from 3 to 20% by weight, preferably from 4 to 10% by weight, of the primer.
  • surfactants may be, for example, surfactants, defoamers, dispersants, sensitisers, stabilisers against deterioration by heat or light, reodorants, flow or slip aids, biocides, optical brighteners and identifying tracers.
  • the surfactant assists with wetting of the substrate surface by the primer, but it can be detrimental to the bonding process of the overlying inkjet ink and so is preferably present at less than 2% by weight, more preferably less than 1 %, based on the total weight of the primer. Most preferably, surfactant is absent from the primer.
  • the method of the present invention includes step (iii) jetting an inkjet ink onto the primer, wherein the inkjet ink comprises one or more multifunctional monomers, a colourant, one or more photoinitiators and optionally one or more multifunctional oligomers, wherein the total weight of the multifunctional monomers combined with, when present, the multifunctional oligomers, is at least 15% by weight based on the total weight of the ink.
  • the inkjet ink of the present invention which is jetted in step (iii) of the method of the present invention, comprises one or more multifunctional monomers, a colourant, one or more photoinitiators and optionally one or more multifunctional oligomers, wherein the total weight of the multifunctional monomers combined with, when present, the multifunctional oligomers, is at least 15% by weight based on the total weight of the ink.
  • the inkjet ink can be prepared by methods well known in the art and so a detailed discussion is not required.
  • the inkjet ink like the primer, is radiation-curable as discussed above.
  • the inkjet ink comprises less than 5% by weight of volatile organic solvent and water combined, preferably less than 3% by weight combined, more preferably, less than 2% by weight combined and most preferably less than 1 % by weight combined, based on the total weight of the inkjet ink.
  • the total weight of the multifunctional monomers combined with, when present, the multifunctional oligomers is at least 15% by weight, based on the total weight of the ink.
  • the total weight of the multifunctional monomers combined with, when present, the multifunctional oligomers is at least 40% by weight, more preferably at least 70% by weight, based on the total weight of the ink.
  • the total weight of the multifunctional monomers combined with, when present, the multifunctional oligomers is no more than 85% by weight, based on the total weight of the ink.
  • the one or more multifunctional monomers and optionally one or more multifunctional oligomers provide sufficient crosslinking in the printed ink film upon curing and hence the hard and solvent- resistant properties of the ink. Further, the multifunctional monomers and multifunctional oligomers have the polarity values required to provide a printed ink film with a high gloss and excellent colour density. All of these properties result in a printed ink film with a highly desirable combination of excellent appearance and physical properties.
  • the multifunctional monomers may be any multifunctional monomer which could be involved in the curing reaction, such as a multifunctional (meth)acrylate monomer, a multifunctional vinyl ether or a multifunctional vinyl (meth)acrylate.
  • Multifunctional (meth)acrylate monomers are well known in the art and a detailed description is therefore not required.
  • Preferred examples include hexanediol diacrylate, polyethylene glycol diacrylate (for example tetraethyleneglycol diacrylate), dipropylene glycol diacrylate, neopentylglycol diacrylate, 3-methyl pentanediol diacrylate, the acrylate esters of ethoxylated or propoxylated glycols and polyols, for example, propoxylated neopentyl glycol diacrylate, trimethylolpropane triacrylate, pentaerythritol triacrylate, tri(propylene glycol) triacrylate, bis(pentaerythritol) hexaacrylate, and the acrylate esters of ethoxylated or propoxylated glycols and polyols, for example, ethoxylated trimethylolpropane triacrylate, and combinations thereof.
  • polyethylene glycol diacrylate for example tetraethyleneglycol diacrylate
  • suitable multifunctional (meth)acrylate monomers also include esters of methacrylic acid (i.e. methacrylates), such as hexanediol dimethacrylate, triethyleneglycol dimethacrylate, diethyleneglycol dimethacrylate, ethyleneglycol dimethacrylate, 1 ,4-butanediol dimethacrylate, trimethylolpropane trimeth acrylate and combinations thereof. Mixtures of (meth)acrylates may also be used. Multifunctional vinyl ethers may also be present in the inkjet ink.
  • Examples are well known in the art and include vinyl ethers such as triethylene glycol divinyl ether, diethylene glycol divinyl ether and 1 ,4- cyclohexanedimethanol divinyl ether. Mixtures of multifunctional vinyl ethers can be used alone or in combination with multifunctional (meth)acrylate monomers. Triethylene glycol divinyl ether is particularly preferred. Multifunctional monomers containing both an acrylate and a vinyl ether reactive group may also be present in the inkjet ink. An example is 2-(2-vinyloxyethoxy) ethyl acrylate (VEEA).
  • VEEA 2-(2-vinyloxyethoxy) ethyl acrylate
  • Monomers typically have a molecular weight of less than 600, preferably more than 150 and less than 450. Monomers are typically added to inkjet inks to reduce the viscosity of the inkjet ink. They therefore preferably have a viscosity of less than 150 mPas at 25°C, more preferably less than 100 mPas at 25°C. Monomer viscosities can be measured using an ARG2 rheometer manufactured by T.A. Instruments, which uses a 40 mm oblique / 2° steel cone at 25°C with a shear rate of 25 s
  • the radiation-curable material of the ink used in the method of the present invention may comprise a radiation-curable (i.e.
  • polymerisable multifunctional oligomer such as a multifunctional (meth)acrylate oligomer.
  • Any radiation-curable multifunctional oligomer that is compatible with the other ink components is suitable for use in the ink.
  • the ink formulator is able to select from a wide range of suitable oligomers.
  • Oligomers are defined hereinabove in relation to the primer. Oligomers are typically added to inkjet inks to increase the viscosity of the inkjet ink. They therefore preferably have a viscosity of 150 mPas or above at 25°C. Preferred oligomers for inclusion in the ink of the invention have a viscosity of 0.5 to 10 Pas at 50°C. Oligomer viscosities can be measured using an ARG2 rheometer manufactured by T.A. Instruments, which uses a 40 mm oblique / 2° steel cone at 60°C with a shear rate of 25 s ⁇ 1 .
  • the multifunctional oligomers may possess different degrees of functionality, and a mixture including combinations of di, tri and higher functionality oligomers may be used.
  • the degree of functionality of the oligomer determines the degree of crosslinking and hence the properties of the cured ink.
  • the oligomer is multifunctional meaning that it contains on average more than one reactive functional group per molecule.
  • the average degree of functionality is preferably from 2 to 6.
  • Radiation-curable multifunctional oligomers comprise a backbone, for example a polyester, urethane, epoxy or polyether backbone, and one or more radiation-curable groups.
  • the backbone will be selected depending on the specific requirements of the printed ink, such as print flexibility, durability etc.
  • the polymerisable group can be any group that is capable of polymerising upon exposure to radiation.
  • the multifunctional oligomers are (meth)acrylate oligomers.
  • radiation-curable oligomers include epoxy based materials such as bisphenol A epoxy acrylates and epoxy novolac acrylates, which have fast cure speeds and provide cured films with good solvent resistance.
  • the one or more multifunctional monomers and optionally one or more multifunctional oligomers comprise multifunctional (meth)acrylates.
  • Multifunctional (meth)acrylates present in the inkjet ink have a strong affinity to the underlying primer, particularly a primer in which the one or more monofunctional monomers are (meth)acrylate monomers.
  • Preferred multifunctional monomers for use in the inkjet ink of the present invention include dipropylene glycol diacrylate (DPGDA), neopentylglycol diacrylate (NPGPODA), triethylene glycol divinyl ether (DVE-3) and combinations thereof.
  • the one or more multifunctional monomers and optionally one or more multifunctional oligomers polymerise by free-radical polymerisation.
  • the one or more multifunctional monomers and optionally one or more multifunctional oligomers cure upon exposure to radiation in the presence of a photoinitiator to form a crosslinked, solid film.
  • Monofunctional monomers may also be present in the inkjet ink.
  • Monofunctional monomers are defined hereinabove in relation to the primer.
  • Monofunctional (meth)acrylate monomers such as PEA and IBOA may be present in 1 -50% by weight, based on the total weight of the ink.
  • N-Vinyl amides such as NVC may be present in 1 -20% by weight, based on the total weight of the ink. Combinations of NVC with the (meth)acrylate monomers set out hereinabove are particularly preferred.
  • the inkjet ink of the present invention which is jetted in step (iii) of the method of the present invention, comprises a colourant.
  • the colouring agent may be either dissolved or dispersed in the liquid medium of the ink.
  • the colouring agent is a dispersible pigment, of the types known in the art and commercially available such as under the trade-names Paliotol (available from BASF pic), Cinquasia, Irgalite (both available from Ciba Speciality Chemicals) and Hostaperm (available from Clariant UK).
  • the pigment may be of any desired colour such as, for example, Pigment Yellow 155, Pigment Yellow 120, Pigment Yellow 13, Pigment Yellow 83, Pigment Red 9, Pigment Red 122, Pigment Red 184, Pigment Orange 34, Pigment Blue 15:3, Pigment Green 7, Pigment Violet 19, Pigment Black 7.
  • Pigment Yellow 155 Pigment Yellow 120, Pigment Yellow 13, Pigment Yellow 83, Pigment Red 9, Pigment Red 122, Pigment Red 184, Pigment Orange 34, Pigment Blue 15:3, Pigment Green 7, Pigment Violet 19, Pigment Black 7.
  • Pigment Yellow 155 Pigment Yellow 120, Pigment Yellow 13, Pigment Yellow 83, Pigment Red 9, Pigment Red 122, Pigment Red 184, Pigment Orange 34, Pigment Blue 15:3, Pigment Green 7, Pigment Violet 19, Pigment Black 7.
  • Pigment Yellow 155 Pigment Yellow 120, Pigment Yellow 13, Pigment Yellow 83, Pigment Red 9, Pigment Red 122, Pigment Red 184, Pigment Orange 34, Pigment Blue 15:3, Pigment Green 7, Pigment Violet 19, Pig
  • Cyan phthalocyanine pigments such as Phthalocyanine blue 15.4.
  • Yellow azo pigments such as Pigment yellow 120, Pigment yellow 151 and Pigment yellow 155.
  • Magenta quinacridone pigments, such as Pigment violet 19 or mixed crystal quinacridones such as Cromophtal Jet magenta 2BC and Cinquasia RT-355D.
  • Black carbon black pigments such as Pigment black 7.
  • Pigment particles dispersed in the ink should be sufficiently small to allow the ink to pass through an inkjet nozzle, typically having a particle size less than 8 ⁇ , preferably less than 5 ⁇ , more preferably less than 1 ⁇ and particularly preferably less than 0.5 ⁇ .
  • the colourant is preferably present in an amount of 10% by weight or less, preferably 5% by weight or less, based on the total weight of the ink.
  • a higher concentration of pigment may be required for white inks, however, for example up to and including 30% by weight, or 15% by weight based on the total weight of the ink.
  • the inks may be in the form of a multi-chromatic inkjet ink set, which typically comprises a cyan ink, a magenta ink, a yellow ink and a black ink (a so-called trichromatic set).
  • Process colour inks can be used to produce a wide range of colours and tones.
  • the inkjet ink of the present invention which is jetted in step (iii) of the method of the present invention, comprises one or more photoinitiators. Suitable photoinitiators are discussed above in relation to the primer.
  • the photoinitiator is present from 3 to 20% by weight, preferably from 4 to 18% by weight, of the inkjet ink.
  • the inkjet ink exhibits a desirable low viscosity, less than 100 mPas, preferably 50 mPas or less and most preferably 30 mPas or less at 25°C.
  • the inkjet ink most preferably has a viscosity of 10 to 30 mPas at 25°C.
  • components of types known in the art may be present in the inkjet ink to improve the properties or performance.
  • These components may be, for example, surfactants, defoamers, dispersants, sensitisers, stabilisers against deterioration by heat or light, reodorants, flow or slip aids, biocides and identifying tracers.
  • the method of the present invention includes step (iv), curing the primer and the inkjet ink.
  • the primer and the inkjet ink are therefore cured by exposure to actinic radiation.
  • the source of actinic radiation can be any source of actinic radiation that is suitable for curing radiation-curable inks but is preferably a UV source. Suitable UV sources include mercury discharge lamps, fluorescent tubes, light emitting diodes (LEDs), flash lamps and combinations thereof. One or more mercury discharge lamps, fluorescent tubes, or flash lamps may be used as the radiation source. When LEDs are used, these are preferably provided as an array of multiple LEDs.
  • a suitable cure dose would be greater than 200 mJ/cm 2 , more preferably at least 300 mJ/cm 2 and most preferably at least 500 mJ/cm 2 .
  • the upper limit is less relevant and will be limited only by the commercial factor that more powerful radiation sources increase cost.
  • a typical upper limit would be 5 J/cm 2 .
  • the method of the present invention comprises the following steps, in order: (i) providing a substrate; (ii) jetting a primer onto the substrate, wherein the primer comprises one or more monofunctional monomers, a passive resin and one or more photoinitiators, wherein the one or more monofunctional monomers are present in at least 85% by weight, based on the total weight of the primer; (iii) pinning the primer; (iv) jetting an inkjet ink onto the primer, wherein the inkjet ink comprises one or more multifunctional monomers, a colourant, one or more photoinitiators and optionally one or more multifunctional oligomers, wherein the total weight of the multifunctional monomers combined with, when present, the multifunctional oligomers, is at least 15% by weight based on the total weight of the ink; and (v) curing the primer and the inkjet ink.
  • Pinning is achieved by exposure to actinic radiation. Suitable sources of actinic radiation are discussed hereinabove in relation to the curing of the primer and the inkjet ink.
  • the dose of actinic radiation for pinning is lower than the dose required for (full) cure, and is typically 1 -200 mJ/cm 2 , preferably 1 -100 mJ/cm 2 and more preferably 1 -50 mJ/cm 2 .
  • Medium pressure mercury lamps may be used as the pinning source.
  • LED lamps may also be used as the pinning source and in this embodiment, the source preferably has a wavelength of 385 or 395 nm.
  • the method of the present invention comprises the following steps, in order: (i) providing a substrate; (ii) jetting a primer onto the substrate, wherein the primer comprises one or more monofunctional monomers, a passive resin and one or more photoinitiators, wherein the one or more monofunctional monomers are present in at least 85% by weight, based on the total weight of the primer; (iii) curing the primer; (iv) jetting an inkjet ink onto the primer, wherein the inkjet ink comprises one or more multifunctional monomers, a colourant, one or more photoinitiators and optionally one or more multifunctional oligomers, wherein the total weight of the multifunctional monomers combined with, when present, the multifunctional oligomers, is at least 15% by weight based on the total weight of the ink; and (v) curing the inkjet ink
  • the present invention also provides a printed substrate obtainable by the method of the present invention as discussed above.
  • the present invention also provides a primer as defined hereinabove in relation to the method of the present invention.
  • the present invention also provides an ink set comprising a primer as defined hereinabove in relation to the method of the present invention and an inkjet ink as defined hereinabove in relation to the method of the present invention.
  • a primer of the invention was prepared.
  • the primer (primer 1) had the formulation as shown in Table 1 .
  • Table 1 Formulation of primer 1
  • 2-PEA, IBOA, CTFA are monofunctional monomers.
  • BR1 13 is a 20% solution of an acrylic copolymer resin with a Mw of 30 kDa and a Tg of 78°C, in 2-PEA, stabilised with 1 % Florstab UV-12. Florstab UV-12 is available from Kromachem and is a stabiliser.
  • Irgacure 184 and Irgacure 819 are photoinitiators.
  • the primer was prepared by first weighing the monofunctional monomers into a suitable mixing vessel, placing the vessel under the mixing head of a Silverson stirrer and starting the stirrer. The resin was added and the mixture stirred until the mixture was homogeneous. The temperature was monitored throughout to ensure that the temperature did not exceed 40°C. The remaining components were added to the mixture and the mixture stirred and heated to 40°C to ensure complete dissolution.
  • Primer 1 had a viscosity of 20.1 mPas at 25°C.
  • Example 2
  • Inkjet inks of the invention were prepared.
  • the inkjet inks (inkjet inks 1 -4) had the formulations as shown in Table 2.
  • DVE-3 and DPGDA are multifunctional monomers.
  • UV-12 is a stabiliser.
  • Irgacure 369, Irgacure 184, Lucirin TPO and Irgacure 2959 are photoinitiators.
  • the cyan, magenta, yellow and black dispersions had the compositions as shown in Table 3.
  • Primer 1 was printed onto high impact polystyrene (HIPS), fluted polypropylene (FPP), polypropylene (PP), acrylic, polycarbonate (PC), self-adhesive vinyl (SAV) and coated paper substrates.
  • Inkjet inks were either printed over primer 1 or printed directly onto the substrates.
  • the inks were commercially available cyan, magenta, yellow, black UV inkjet inks from Fujifilm falling within the scope of the inkjet ink used in the method of the present invention.
  • Primer and ink were printed onto the substrates using an Acuity 4008 using Quality Layered mode, wherein the primer was the lower third of the image.
  • the image consisted of cyan, magenta, yellow, black blocks.
  • the substrates were provided by Stephen Webster Plastics (SWP).
  • SWP Stephen Webster Plastics
  • the HIPS was 2 mm gloss filmed one side/matte reverse.
  • the FPP was 3 mm thick with the trade name Correx.
  • the PP was A2 Vi- print white 1 155, 0.5 mm thick.
  • the acrylic was supplied to SWP by Altuglas.
  • the PC was 2 mm 10 year Lexan Red.
  • the SAV was Avery 400 Permanent, 0.5 mm thick.
  • the coated paper was I/O paper from Oce.
  • Hardness was tested using a Taber Reciprocating Abraser (Abrader), Model 5900 fitted with a round wire loop stylus.
  • the printed substrates were subjected to five cycles at 30 cycles per minute using three weights of 1 , 2 and 2.5 N. Each printed substrate was tested shortly after printing and more than 16 hours after printing.
  • the scores for each weight are added together to give a final score of 15-3.
  • Blocking was tested using three sheets of coated paper substrate. Each test ink was applied to three sheets of coated paper.
  • the three sheets of printed coated paper were stacked in such a way to facilitate assessment of both ink to paper and ink to ink blocking.
  • the stack of paper was covered by an A4 size plate and 20 kg placed on top of the stack for more than 16 hours. At the end of this period, the weight was removed and the three sheets of printed coated paper separated.
  • Solvent resistance was tested using the isopropyl alcohol (IPA) rub test. Using a lint-free (cotton) cloth saturated in IPA, a double rub is applied to the surface of the printed substrate under light pressure, traversing the length of the surface of the printed substrate in a back and forth motion. The number of double rubs is counted until the substrate is visible. Table 4. Testing of adhesion, hardness, blocking and solvent resistance with and without primer 1
  • Primer 1 was applied to PC, acrylic and FPP substrates via drawdown using an RK coater and a K2 bar (12 ⁇ wet film).
  • the primed substrates were cured using a Jenton dryer fitted with an Oce mercury lamp from an Arizona 550 at power level 7 at 40 m/min with two passes.
  • Inkjet ink 1 containing a cyan pigment was applied either over primer 1 or directly onto the substrates via drawdown using an RK coater and a K2 bar (12 ⁇ wet film).
  • the printed ink films were cured using a Jenton dryer fitted with an Oce mercury lamp from an Arizona 550 at power level 7 at 40 m/min with four passes.
  • the printed substrates were assessed for adhesion, folding and cutting. The results are shown in Table 5.
  • the fold test involves cutting along the flute on the opposite side of the substrate to the ink and folding backwards five times.
  • the printed substrates pass if no ink is lost along the fold or the printed substrates fail if ink is lost along the fold.
  • the cut test involves cutting across the flute on the inked side and scratching the cut edge with a fingernail.
  • the printed substrates pass if no ink is lost along the cut edge or the printed substrates fail if ink is lost along the cut edge.
  • primers 2-5 A number of comparative primers not containing a passive resin were prepared.
  • the primers (primers 2-5) had the formulations as shown in Table 6. Table 6. Formulations of primers 2-5
  • CN371 is a difunctional amine co-initiator.
  • CN964A85 is an aliphatic polyester-based urethane diacrylate oligomer blended with 15% SR306, tripropylene glycol diacrylate.
  • CN2560 is a tetrafunctional polyester acrylate.
  • Genomer 5696 is a hexafunctional acrylated oligoamine resin.
  • Primers 2-5 were prepared as in Example 1 .
  • Example 6 Primers 1 -5 were applied to PC, acrylic and FPP substrates and cured as in Example 4. Inkjet ink 1 was applied over primers 1 -5 and cured as in Example 4.
  • the printed substrates containing the primer of the invention showed good adhesion and passed the fold and the cut tests. All of the printed substrates containing comparative primers (primers 2-5) did not perform as well in the fold and cut tests and all of the printed substrates adhered poorly to the three substrates tested, apart from the printed substrate containing primer 3 which only showed poor adhesion to FPP.
  • primers of the invention were prepared.
  • the primers (primers 6-9) had the formulations as shown in Table 8.
  • Primers 6-9 were prepared as in Example 1 .
  • Example 8 Primers 1 and 6-9 were applied to PC, acrylic, FPP and SAV substrates and cured as in Example 4. Inkjet ink 1 was applied over the primers and cured as in Example 4.
  • the printed substrates were assessed for adhesion and hardness. Adhesion and hardness were tested as in Example 3.
  • Primer 6 contains 15% CTFA, primer 1 contains 20% CTFA, primer 7 contains 25% CTFA, primer 8 contains 30% CTFA and primer 9 contains 35% CTFA.
  • CTFA contains approximately 5% trimethylolpropane triacrylate (TMPTA), a multifunctional monomer, as a reaction by-product.
  • Primer 1 contains 1 % TMPTA.
  • Primers 6-9 contain between 0.75 and 1 .75% TMPTA as detailed above in Table 8. As the amount of CTFA in the primer increases and hence the amount of multifunctional monomer in the primer increases, the adhesion of the printed substrate decreases. The TMPTA contamination gives an indication of the tolerance of the primer to multifunctional monomers as tested on certain substrates. The hardness of the overlying inkjet ink was not affected.
  • primers of the invention were prepared.
  • the primers (primers 10-13) had the formulations as shown in Table 9.
  • EOEOEA is a monofunctional monomer with a glass transition temperature of -70°C.
  • Primers 10-13 were prepared as in Example 1 .
  • the printed substrates were assessed for adhesion and hardness as in Example 3.
  • Primer 10 contains no EOEOEA
  • primer 1 1 contains 5% EOEOEA
  • primer 12 contains 10% EOEOEA
  • primer 13 contains 15% EOEOEA.
  • EOEOEA has a glass transition temperature of -70°C.
  • Primer 1 was contaminated with 5% DPGDA (a multifunctional monomer).
  • the resultant primer (primer 14) had the formulation as shown in Table 10. Table 10. Formulation of primer 14
  • Primer 14 was prepared as in Example 1 .
  • Primer 14 was applied onto FPP, PC and acrylic and cured as in Example 4.
  • Inkjet ink 1 was applied over the primer and cured as in Example 4. Adhesion and hardness were tested as in Example 3.
  • the primer and the ink will have fully cured leading to some shrinkage.
  • the contamination with DPGDA produces leaching of a multifunctional monomer from the overlying inkjet ink into the primer before final cure.
  • the adhesion to FPP is adversely affected at this very high level of contamination after 0 and 16 hours.
  • the adhesion to PC is still very good after 0 and 16 h.
  • the adhesion to acrylic is still very good after 0 h but is less good after 16 h.
  • the passive resin can to some extent protect the primer from leaching of multifunctional monomers from the overlying ink.
  • the hardness properties of the printed inks were not affected by the amount of multifunctional monomer that was present in primers 14.

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Abstract

La présente invention concerne un procédé d'impression à jet d'encre comprenant les étapes suivantes consistant à, dans l'ordre : (i) fournir un substrat ; (ii) projeter un apprêt sur le substrat, l'apprêt comprenant un ou plusieurs monomères monofonctionnels, une résine passive et un ou plusieurs photo-initiateurs, ledit monomère monofonctionnel étant présent en une proportion d'au moins 85 % en poids du poids total de l'apprêt ; (iii) projeter une encre pour jet d'encre sur l'apprêt, l'encre pour jet d'encre comprenant un ou plusieurs monomères multifonctionnels, un colorant, un ou plusieurs photo-initiateurs et éventuellement un ou plusieurs oligomères multifonctionnels, le poids total des monomères multifonctionnels combinés aux oligomères multifonctionnels, lorsque ceux-ci sont présents, étant d'au moins 15 % en poids du poids total de l'encre ; et (iv) durcir l'apprêt et l'encre pour jet d'encre. La présente invention concerne également un substrat imprimé pouvant être obtenu par le procédé selon la présente invention, un apprêt tel qu'utilisé dans le procédé selon la présente invention, et un ensemble d'encres comprenant un apprêt tel qu'utilisé dans le procédé selon la présente invention et une encre pour jet d'encre telle qu'utilisée dans le procédé selon la présente invention.
PCT/GB2017/052555 2016-09-02 2017-09-01 Procédé d'impression Ceased WO2018042193A1 (fr)

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EP4004131B1 (fr) 2019-12-04 2023-03-15 Sun Chemical Corporation Compositions pour jet d'encre uv
EP4151411A4 (fr) * 2020-05-13 2023-11-08 FUJIFILM Corporation Ensemble d'encres, procédé d'impression d'image, et imprimé

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US12116490B2 (en) * 2021-04-08 2024-10-15 Sun Chemical Corporation Low migration EB curable inks with bio-renewable content

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EP2653509A1 (fr) * 2010-12-17 2013-10-23 Hitachi Maxell, Ltd. Apprêt pour enregistrement à jet d'encre
JP2015009392A (ja) * 2013-06-27 2015-01-19 富士フイルム株式会社 インクジェット記録方法

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EP2653509A1 (fr) * 2010-12-17 2013-10-23 Hitachi Maxell, Ltd. Apprêt pour enregistrement à jet d'encre
JP2013043894A (ja) * 2011-08-22 2013-03-04 Dnp Fine Chemicals Co Ltd 下塗り液、下塗り層、及びインクジェット記録方法
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EP4004131B1 (fr) 2019-12-04 2023-03-15 Sun Chemical Corporation Compositions pour jet d'encre uv
EP4004131B2 (fr) † 2019-12-04 2025-07-23 Sun Chemical B.V. Compositions pour jet d'encre uv
WO2021211662A1 (fr) * 2020-04-15 2021-10-21 Sun Chemical Corporation Procédé d'amélioration du durcissement actinique d'encres et de revêtements durcissables par application d'énergie
JP2023515258A (ja) * 2020-04-15 2023-04-12 サン ケミカル コーポレイション エネルギー硬化性インク及びコーティングの化学線硬化を改善する方法
JP7381774B2 (ja) 2020-04-15 2023-11-16 サン ケミカル コーポレイション エネルギー硬化性インク及びコーティングの化学線硬化を改善する方法
US11976202B2 (en) 2020-04-15 2024-05-07 Sun Chemical Corporation Method of improving actinic cure of energy curable inks and coatings
US12331203B2 (en) 2020-04-15 2025-06-17 Sun Chemical Corporation Method of improving actinic cure of energy curable inks and coatings
EP4151411A4 (fr) * 2020-05-13 2023-11-08 FUJIFILM Corporation Ensemble d'encres, procédé d'impression d'image, et imprimé
US12269959B1 (en) 2020-05-13 2025-04-08 Fujifilm Corporation Ink set, image recording method, and recorded article

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