WO2022090718A1 - Encre d'impression - Google Patents

Encre d'impression Download PDF

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Publication number
WO2022090718A1
WO2022090718A1 PCT/GB2021/052796 GB2021052796W WO2022090718A1 WO 2022090718 A1 WO2022090718 A1 WO 2022090718A1 GB 2021052796 W GB2021052796 W GB 2021052796W WO 2022090718 A1 WO2022090718 A1 WO 2022090718A1
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WO
WIPO (PCT)
Prior art keywords
ink
weight
inkjet ink
radiation
aminoketone
Prior art date
Application number
PCT/GB2021/052796
Other languages
English (en)
Inventor
Lee CORFE
Original Assignee
Fujifilm Speciality Ink Systems Limited
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 GBGB2017159.1A external-priority patent/GB202017159D0/en
Priority claimed from GBGB2017869.5A external-priority patent/GB202017869D0/en
Priority claimed from GBGB2109028.7A external-priority patent/GB202109028D0/en
Application filed by Fujifilm Speciality Ink Systems Limited filed Critical Fujifilm Speciality Ink Systems Limited
Priority to GB2307522.9A priority Critical patent/GB2615930A/en
Publication of WO2022090718A1 publication Critical patent/WO2022090718A1/fr

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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
    • 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
    • C09D11/38—Inkjet printing inks characterised by non-macromolecular additives other than solvents, pigments or dyes

Definitions

  • the present invention relates to a printing ink and, in particular, to an inkjet ink which is suitable for food packaging applications.
  • 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 For high-speed printing, the inks must flow rapidly from the printing heads, and, to ensure that this happens, they must have in use a low viscosity, typically 200 mPas or less at 25°C, although in most applications the viscosity should be 50 mPas or less, and often 25 mPas or less.
  • the ink when ejected through the nozzles, the ink has a viscosity of less than 25 mPas, preferably 5-15 mPas and most preferably between 7-1 1 mPas at the jetting temperature, which is often elevated to, but not limited to 40-50°C (the ink might have a much higher viscosity at ambient temperature).
  • inks must also be resistant to drying or crusting in the reservoirs or nozzles.
  • inkjet inks for application at or near ambient temperatures are commonly formulated to contain a large proportion of a mobile liquid vehicle or solvent such as water or a low-boiling solvent or mixture of solvents.
  • inkjet ink contains unsaturated organic compounds, termed monomers and/or oligomers, which polymerise when cured.
  • This type of ink has the advantage that it is not necessary to evaporate the liquid phase to dry the print; instead the print is cured, a process which is more rapid than evaporation of solvent at moderate temperatures.
  • Inkjet inks can be printed onto a variety of substrates. Particularly challenging substrates for inkjet printing thereon are substrates for food packaging.
  • Food packaging represents a particular challenge because of the strict safety limitations on the properties of materials that come into contact with food, including indirect additives like packaging inks. Accordingly, for printed food packaging, it is necessary to control and quantify the migration and/or odour of the components of the printed image on the food packaging into the food products. Specific exclusions based on their odour and/or migration properties include volatile organic solvents and many monomers typically used in curable inks.
  • an inkjet ink it is also advantageous for an inkjet ink to have a high cure speed for food packaging applications, in particular for single pass printing onto food packaging.
  • cure speed is meant the speed at which the actinic radiation source moves relative to the substrate.
  • An advantage of a high cure speed is that a low dose per unit area is required to achieve a fully cured film.
  • sources of actinic radiation which are commonly used to cure inkjet inks which contain radiation-curable material.
  • the most common source of radiation is a UV source. UV sources include mercury discharge lamps, fluorescent tubes, light emitting diodes (LEDs), flash lamps and combinations thereof.
  • LED UV light sources are an attractive alternative.
  • LEDs offer significant cost reduction, longer maintenance intervals, higher energy efficiency and are an environmentally friendlier solution.
  • LEDs When LEDs are used, it is necessary to use an array of multiple LEDs in order to generate enough powerto provide thorough curing of the ink. In fact, even with an array of multiple LEDs, inks which are cured by LEDs are prone to poor surface cure owing to the presence of oxygen in the atmosphere adjacent to the ink surface, and the spectral output of LEDs. Compared to conventional mercury lamp UV sources, LEDs have a narrow spectral output. The UV output of LED lamps is essentially monochromatic and most commercial devices operate at 385, 395 or 405 nm. LEDs emit radiation in the UVA region having a long wavelength over a narrow range of wavelengths, which although suitable for depth cure, provides a particular challenge for effective surface cure in normal atmospheric conditions.
  • Poor surface cure can be reduced in a number of ways. First, it can be overcome by blanketing the irradiated area with an inert gas such as nitrogen during the cure process but this adds considerably to the complexity and cost of the printer. Secondly, it can be overcome by working the LEDs at high power, providing more energy to react with the photoinitiators and oxygen, or the total amount of photoinitiators may be increased, thus allowing more radicals to be generated. However, working the LEDs at high power generates heat, which must be removed and both approaches add to the cost and complexity of the process - regard must be had to limitations on the media range, power consumption, ink viscosity and ink stability. Thirdly, a blend of photoinitiators may be used. However, there are a limited number of blends of photoinitiators that are suitable for food packaging applications.
  • the present invention provides an inkjet ink comprising a radiation-curable material and a photoinitiator package, wherein the photoinitiator package comprises: (i) 4.5 to 12.0% by weight of one or more polymeric a-aminoketone photoinitiators;
  • the inventors have surprisingly found that the inclusion of the photoinitiator package as claimed comprising the specific blend of photoinitiators in the specific amounts provides an inkjet ink that can be printed onto food packaging having low migration and odour, and which has a high UV LED cure speed and good surface cure.
  • the inkjet ink of the present invention comprises a radiation-curable material.
  • the radiation-curable material is not particularly limited and the formulator is free to include any such radiation-curable material in the ink of the present invention to improve the properties or performance of the ink.
  • This radiation-curable material can include any radiation-curable material readily available and known in the art in inkjet inks.
  • radiation-curable is meant a material that polymerises and/or crosslinks upon irradiation, for example, when exposed to actinic radiation, in the presence of a photoinitiator.
  • the amount of radiation-curable material is not limited other than by the constraints imposed by the use in an inkjet ink, such as viscosity, stability, toxicity etc.
  • the inkjet ink comprises 20 to 90% by weight of radiation-curable material, based on the total weight of the ink.
  • the inkjet ink comprises radiation-curable material that is suitable for printing onto food packaging.
  • the inkjet ink comprises a radiation-curable monomer.
  • monomers may possess different degrees of functionality, which include mono, di, tri and higher functionality monomers.
  • the inkjet ink comprises a di- and/or multifunctional radiation-curable monomer.
  • mono and difunctional are intended to have their standard meanings, i.e. one or two groups, respectively, which take part in the polymerisation reaction on curing.
  • Multifunctional (which does not include difunctional) is intended to have its standard meaning, i.e. three or more groups, respectively, which take part in the polymerisation reaction on curing.
  • the radiation-curable monomer is a di-, tri-, tetra-, penta- or hexafunctional monomer, i.e. the radiation curable monomer has two, three, four, five or six functional groups.
  • the inkjet ink comprises a difunctional monomer.
  • the inkjet ink comprises at least two di- and/or multifunctional radiation-curable monomers and more preferably, at least two difunctional monomers.
  • the functional group of the di- and/or multifunctional radiation-curable monomer, which is utilised in the ink of the present invention may be the same or different but must take part in the polymerisation reaction on curing.
  • Examples of such functional groups include any groups that are capable of polymerising upon exposure to radiation and are preferably selected from a (meth)acrylate group and a vinyl ether group.
  • the di- and/or multifunctional radiation-curable monomer may possess different degrees of functionality, and a mixture including combinations of di, tri and higher functionality monomers may be used.
  • the substituents of the di- and/or multifunctional radiation-curable monomer are not limited other than by the constraints imposed by the use in an ink-jet ink, 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 C1-18 alkyl, C3-18 cycloalkyl, CB- aryl and combinations thereof, such as Cs- aryl- or C3-18 cycloalkyl-substituted C1-18 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.
  • the inkjet ink comprises 5 to 90% by weight of a di- and/or multifunctional radiation-curable monomer, based on the total weight of the ink.
  • di- and/or multifunctional radiation-curable monomer examples include difunctional (meth)acrylate monomers, multifunctional (meth)acrylate monomers, divinyl ether monomers, multifunctional vinyl ether monomers and di- and/or multifunctional vinyl ether (meth)acrylate monomers. Mixtures of di- and/or multifunctional radiation-curable monomers may also be used.
  • the radiation-curable material comprises a (meth)acrylate monomer, more preferably a di- and/or multifunctional (meth)acrylate monomer.
  • the inkjet ink comprises a difunctional (meth)acrylate monomer.
  • (meth)acrylate is intended herein to have its standard meaning, i.e. acrylate and/or methacrylate.
  • Difunctional (meth)acrylate monomers are well known in the art and a detailed description is therefore not required. Examples include hexanediol diacrylate (HDDA), 1 ,8-octanediol diacrylate, 1 ,9-nonanediol diacrylate, 1 ,10-decanediol diacrylate (DDDA), 1 ,11-undecanediol diacrylate and 1 ,12-dodecanediol diacrylate, polyethylene glycol diacrylate (for example tetraethylene glycol diacrylate, PEG200DA, PEG300DA, PEG400DA, PEG600DA), dipropylene glycol diacrylate (DPGDA), tripropylene glycol diacrylate (TPGDA), tricyclodecane dimethanol diacrylate (TCDDMDA), neopentylglycol diacrylate, 3-methyl-1 ,5-pentanediol diacrylate (3-MP
  • esters of methacrylic acid such as hexanediol dimethacrylate, 1 ,8-octanediol dimethacrylate, 1 ,9-nonanediol dimethacrylate, 1 ,10-decanediol dimethacrylate, 1 ,11- undecanediol dimethacrylate and 1 ,12-dodecanediol dimethacrylate, triethyleneglycol dimethacrylate, diethyleneglycol dimethacrylate, ethyleneglycol dimethacrylate, 1 ,4-butanediol dimethacrylate and mixtures thereof.
  • 3-MPDDA is particularly preferred.
  • the inkjet ink comprises 5 to 90% by weight, more preferably 25-85% by weight, more preferably 40-80% by weight of a difunctional (meth)acrylate monomer, based on the total weight of the ink.
  • the inkjet ink may comprise a multifunctional (meth)acrylate monomer.
  • Suitable multifunctional (meth)acrylate monomers include tri-, tetra-, penta-, hexa-, hepta- and octa-functional monomers.
  • multifunctional acrylate monomers examples include trimethylolpropane triacrylate, dipentaerythritol 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 ethoxylated pentaerythritol tetraacrylate (EOPETTA, also known as PPTTA), and mixtures thereof.
  • Suitable multifunctional (meth)acrylate monomers also include esters of methacrylic acid (i.e. methacrylates), such as trimethylolpropane trimethacrylate. Mixtures of (meth)acrylates may also be used.
  • the amount of the multifunctional (meth)acrylate monomer, when present, is preferably 5-25% by weight, based on the total weight of the ink.
  • the di- and/or multifunctional radiation-curable monomer may have at least one vinyl ether functional group.
  • the inkjet ink comprises a divinyl ether monomer, a multifunctional vinyl ether monomer, a divinyl ether (meth)acrylate monomer and/or a multifunctional vinyl ether (meth)acrylate monomer.
  • the inkjet ink comprises a divinyl ether monomer.
  • Examples of a divinyl ether monomer include triethylene glycol divinyl ether (DVE-3), diethylene glycol divinyl ether, 1 ,4-cyclohexanedimethanol divinyl ether, bis[4-(vinyloxy)butyl] 1 ,6- hexanediylbiscarbamate, bis[4-(vinyloxy)butyl] isophthalate, bis[4-(vinyloxy)butyl] (methylenedi- 4,1-phenylene)biscarbamate, bis[4-(vinyloxy)butyl] succinate, bis[4-(vinyloxy)butyl]terephthalate, bis[4-(vinyloxymethyl)cyclohexylmethyl] glutarate, 1 ,4-butanediol divinyl ether and mixtures thereof.
  • Triethylene glycol divinyl ether (DVE-3) is particularly preferred.
  • An example of a multifunctional vinyl ether monomer is tris[4-(vinyloxy)butyl] trimellitate.
  • Examples of a vinyl ether (meth)acrylate monomer include 2-(2-vinyloxy ethoxy)ethyl acrylate (VEEA), 2-(2-vinyloxy ethoxy)ethyl methacrylate (VEEM) and mixtures thereof.
  • VEEA 2-(2-vinyloxy ethoxy)ethyl acrylate
  • VEEM 2-(2-vinyloxy ethoxy)ethyl methacrylate
  • the di- and/or multifunctional radiation-curable monomer is selected from 1 ,10-decanediol diacrylate (DDDA), hexanediol diacrylate (HDDA), polyethylene glycol diacrylate, tripropylene glycol diacrylate (TPGDA), 3-methyl 1 ,5- pentanediol diacrylate (3-MPDA), dipropylene glycol diacrylate (DPGDA), tricyclodecane dimethanol diacrylate (TCDDMDA), propoxylated neopentyl glycol diacrylate (NPGPODA), trimethylolpropane triacrylate (TMPTA), ditrimethylolpropane tetraacrylate (DiTMPTA), di-pentaerythritol hexaacrylate (DPHA), ethoxylated trimethylolpropane triacrylate (EOTMPTA), ethoxylated pentaerythritol tetraacrylate
  • the di- and/or multifunctional radiation-curable monomer is preferably selected from 1 ,10-decanediol diacrylate (DDDA), ethoxylated (5) hexanediol diacrylate (HD(EO)DA), polyethylene glycol (600) diacrylate (PEG600DA), tripropylene glycol diacrylate (TPGDA), 3-methyl 1 ,5-pentanediol diacrylate (3-MPDA), tricyclodecane dimethanol diacrylate (TCDDMDA), propoxylated neopentyl glycol diacrylate (NPGPODA), di-trimethylolpropane tetraacrylate (DiTMPTA), di-pentaerythritol hexaacrylate (DPHA), ethoxylated trimethylolpropane triacrylate (EOTMPTA), ethoxylated pentaerythritol tetraacrylate (EOPETTA),
  • DDDA
  • the difunctional monomer when present, is selected from 1 ,10- decanediol diacrylate (DDDA), hexanediol diacrylate (HDDA), polyethylene glycol diacrylate, tripropylene glycol diacrylate (TPGDA), 3-methyl 1 ,5- pentanediol diacrylate (3-MPDA), dipropylene glycol diacrylate (DPGDA), tricyclodecane dimethanol diacrylate (TCDDMDA), propoxylated neopentyl glycol diacrylate (NPGPODA), triethylene glycol divinyl ether (DVE-3) and mixtures thereof.
  • DDDA 1 ,10- decanediol diacrylate
  • HDDA hexanediol diacrylate
  • TPGDA tripropylene glycol diacrylate
  • DPGDA dipropylene glycol diacrylate
  • the difunctional monomer when present, is preferably selected from 1 ,10-decanediol diacrylate (DDDA), ethoxylated (5) hexanediol diacrylate (HD(EO)DA), polyethylene glycol (600) diacrylate (PEG600DA), tripropylene glycol diacrylate (TPGDA), 3-methyl 1 ,5-pentanediol diacrylate (3- MPDA), tricyclodecane dimethanol diacrylate (TCDDMDA), propoxylated neopentyl glycol diacrylate (NPGPODA), triethylene glycol divinyl ether (DVE-3) and mixtures thereof.
  • DDDA 1 ,10-decanediol diacrylate
  • HD(EO)DA ethoxylated (5) hexanediol diacrylate
  • PEG600DA polyethylene glycol (600) diacrylate
  • TPGDA tripropylene glycol diacrylate
  • the difunctional monomer when present, comprises 3-methyl 1 ,5-pentanediol diacrylate (3-MPDA) and triethylene glycol divinyl ether (DVE-3).
  • 3-MPDA 3-methyl 1 ,5-pentanediol diacrylate
  • DVE-3 triethylene glycol divinyl ether
  • Monomers typically have a molecular weight of less than 600, preferably more than 200 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 100mPas at 25°C and most preferably less than 20 mPas at 25°C. Monomer viscosities can be measured using an ARG2 rheometer manufactured by T.A. Instruments, which uses a 40 mm oblique 12° steel cone at 25°C with a shear rate of 25 s 1 .
  • the inkjet ink may further comprise a monofunctional monomer, such as a monofunctional (meth)acrylate monomer.
  • a radiation-curable monofunctional monomer has one functional group, which takes part in the polymerisation reaction on curing.
  • the polymerisable groups can be any group that are capable of polymerising upon exposure to radiation and are preferably selected from a (meth)acrylate group and a vinyl ether group.
  • the substituents of the monofunctional monomer are not limited other than by the constraints imposed by the use in an inkjet ink, 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 C1-18 alkyl, C3-18 cycloalkyl, CB- aryl and combinations thereof, such as Cs- aryl- or C3-18 cycloalkylsubstituted C1-18 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.
  • the amount of monofunctional monomer, when present, is preferably 1-30% by weight, more preferably 5-25% by weight, based on the total weight of the ink.
  • the inkjet ink may comprise a monofunctional (meth)acrylate monomer, which are well known in the art and are preferably the esters of acrylic acid. A detailed description is therefore not required. Mixtures of (meth)acrylates may also be used.
  • the substituents of the monofunctional (meth)acrylate monomer are not limited other than by the constraints imposed by the use in an inkjet ink, such as viscosity, stability, toxicity etc.
  • the monofunctional (meth)acrylate monomer may be a cyclic monofunctional (meth)acrylate monomer and/or an acyclic-hydrocarbon monofunctional (meth)acrylate monomer.
  • the monofunctional (meth)acrylate monomer may comprise a cyclic monofunctional (meth)acrylate monomer.
  • the substituents of the cyclic monofunctional (meth)acrylate monomer are typically cycloalkyl, aryl and combinations thereof, any of which may be interrupted by heteroatoms and/or substituted by alkyl.
  • substituents commonly used in the art include C3-18 cycloalkyl, Ce- 10 aryl and combinations thereof, any of which may substituted with alkyl (such as C1-18 alkyl) and/or 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.
  • the cyclic monofunctional (meth)acrylate monomer may be selected from isobornyl acrylate (IBOA), phenoxyethyl acrylate (PEA), cyclic TMP formal acrylate (CTFA), tetrahydrofurfuryl acrylate (THFA), (2-methyl-2-ethyl-1 ,3-dioxolane-4-yl)methyl acrylate (MEDA/Medol-10), 4-terf- butylcyclohexyl acrylate (TBCHA), 3,3,5-trimethylcyclohexyl acrylate (TMCHA), benzyl acrylate (BA) and mixtures thereof.
  • the cyclic monofunctional (meth)acrylate monomer comprises benzyl acrylate (BA).
  • the monofunctional (meth)acrylate monomer may comprise an acyclic-hydrocarbon monofunctional (meth)acrylate monomer.
  • the substituents of the acyclic-hydrocarbon monofunctional (meth)acrylate monomer are typically alkyl, which may be interrupted by heteroatoms.
  • a non-limiting example of a substituent commonly used in the art is C1-18 alkyl, which may be interrupted by 1-10 heteroatoms, such as oxygen or nitrogen, with nitrogen further substituted.
  • the acyclic-hydrocarbon monofunctional (meth)acrylate monomer contains a linear or branched C6-C20 group. It may be selected from octadecyl acrylate (ODA), 2-(2-ethoxyethoxy)ethyl acrylate, tridecyl acrylate (TDA), isodecyl acrylate (IDA), lauryl acrylate and mixtures thereof.
  • ODA octadecyl acrylate
  • TDA tridecyl acrylate
  • IDA isodecyl acrylate
  • lauryl acrylate and mixtures thereof.
  • the acyclic-hydrocarbon monofunctional (meth)acrylate monomer contains a linear C6-C20 group.
  • the acyclic-hydrocarbon monofunctional (meth)acrylate monomer comprises lauryl acrylate.
  • the monofunctional (meth)acrylate monomer is selected from isobornyl acrylate (IBOA), phenoxyethyl acrylate (PEA), cyclic TMP formal acrylate (CTFA), tetra hydrofurfuryl acrylate (THFA), (2-methyl-2-ethyl-1 ,3-dioxolane-4-yl)methyl acrylate (MEDA/Medol-10), 4-terf-butylcyclohexyl acrylate (TBCHA), 3,3,5-trimethylcyclohexyl acrylate (TMCHA), benzyl acrylate (BA), octadecyl acrylate (ODA), 2-(2-ethoxyethoxy)ethyl acrylate, tridecyl acrylate (TDA), isodecyl acrylate (IDA), lauryl acrylate and mixtures thereof.
  • IBOA isobornyl acrylate
  • PEA phenoxyethyl acrylate
  • the monofunctional (meth)acrylate monomer comprises benzyl acrylate (BA), lauryl acrylate and mixtures thereof.
  • BA benzyl acrylate
  • lauryl acrylate is particularly preferred monofunctional (meth)acrylate monomers for indirect food contact applications owing to their high migration limits.
  • the inkjet ink comprises a monofunctional (meth)acrylate monomer present in 1-30% by weight, more preferably 5-25% by weight, based on the total weight of the ink.
  • Tetrahydrofurfuryl acrylate is often used to provide good adhesion to variety of substrates, as well as producing a flexible film which is less liable to cracking and delamination.
  • a further advantage of THFA is that it can solubilise chlorinated polyolefins, which in turn provides good adhesion to polyolefin substrates.
  • THFA is a hazardous monomer and bears the GHS hazard statement H314 (Causes severe skin burns and eye damage). There is also growing evidence that it may damage fertility or the unborn child. Thus, there is an urgent need in the art to move away from THFA.
  • the ink will still function in the presence of tetra hydrofurfuryl acrylate (THFA), in terms of its printing and curing properties.
  • THFA tetra hydrofurfuryl acrylate
  • the ink preferably contains less than 2% by weight, more preferably less than 1 % by weight and most preferably is substantially free of THFA, where the amounts are based on the total weight of the ink.
  • substantially free is meant that only small amounts will be present, for example as impurities in the radiation-curable materials present or as a component in a commercially available pigment dispersion.
  • no THFA is intentionally added to the ink.
  • minor amounts of THFA which may be present as impurities in commercially available inkjet ink components, are tolerated.
  • the ink may comprise less than 0.5% by weight of THFA, more preferably less than 0.1 % by weight of THFA, most preferably less than 0.05% by weight of THFA, based on the total weight of the ink.
  • the inkjet ink is free of THFA.
  • the Swiss Ordinance on Materials and Articles in Contact with Food sets out provisions for inks.
  • Annex 10 lists permitted substances for the production of food packaging inks. Substances not listed should not be used for food packaging inks. Caution should still be used for some substances on the Swiss Ordinance list and there is some concern about the quality and safety of the monofunctional (meth)acrylate monomers isodecyl acrylate (IDA), octyl acrylate, phenoxyethyl acrylate (PEA) and 2-ethylhexyl acrylate (2- EHA).
  • IDA isodecyl acrylate
  • PEA phenoxyethyl acrylate
  • 2- EHA 2-ethylhexyl acrylate
  • the ink preferably contains less than 2% by weight, more preferably less than 1 % by weight and most preferably is substantially free of each of IDA, octyl acrylate, PEA and 2-EHA, where the amounts are based on the total weight of the ink. More preferably, the ink contains less than 5% by weight, more preferably less than 2% by weight, more preferably less than 1 % by weight and most preferably is substantially free of IDA, octyl acrylate, PEA and 2-EHA in combination, where the amounts are based on the total weight of the ink.
  • substantially free is meant that only small amounts will be present, for example as impurities in the radiation-curable materials present or as a component in a commercially available pigment dispersion.
  • no IDA, octyl acrylate, PEA and 2-EHA is intentionally added to the ink.
  • minor amounts of IDA, octyl acrylate, PEA and 2-EHA which may be present as impurities in commercially available inkjet ink components, are tolerated.
  • the ink may comprise less than 0.5% by weight of each of IDA, octyl acrylate, PEA and 2-EHA, more preferably less than 0.1 % by weight of each of IDA, octyl acrylate, PEA and 2-EHA, most preferably less than 0.05% by weight of each of IDA, octyl acrylate, PEA and 2-EHA, based on the total weight of the ink.
  • the ink may comprise less than 0.5% by weight of IDA, octyl acrylate, PEA and 2- EHA in combination, more preferably less than 0.1 % by weight of IDA, octyl acrylate, PEA and 2- EHA in combination, most preferably less than 0.05% by weight of IDA, octyl acrylate, PEA and 2- EHA in combination, based on the total weight of the ink.
  • the inkjet ink is free of IDA, octyl acrylate, PEA and 2-EHA.
  • the monofunctional (meth)acrylate monomer is the sole monofunctional monomer present in the ink.
  • the radiation-curable material comprises a di- and/or multifunctional radiation-curable monomer and a monofunctional monomer.
  • the radiation-curable material consists of a di- and/or multifunctional radiation-curable monomer and a monofunctional monomer.
  • the radiation-curable material comprises a difunctional monomer and a monofunctional monomer.
  • the radiation-curable material consists of a difunctional monomer and a monofunctional monomer.
  • the radiation-curable material comprises a difunctional monomer and a monofunctional (meth)acrylate monomer.
  • the radiation-curable material consists of a difunctional monomer and a monofunctional (meth)acrylate monomer.
  • the ink may further include at least one N-vinyl amide monomer and/or N-(meth)acryloyl amine monomer.
  • N-Vinyl amide monomers are well-known monomers in the art.
  • N-Vinyl amide monomers have a vinyl group attached to the nitrogen atom of an amide which may be further substituted in an analogous manner to the (meth)acrylate monomers.
  • Preferred examples are N-vinyl caprolactam (NVC), N-vinyl pyrrolidone (NVP), N-vinyl piperidone, N-vinyl formamide and N-vinyl acetamide.
  • N-acryloyl amine monomers are also well-known in the art.
  • N-Acryloyl amine monomers 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 the (meth)acrylate monomers.
  • a preferred example is N-acryloylmorpholine (ACMO).
  • the inkjet ink preferably comprises at least one of NVC and/or ACMO.
  • N-Vinyl amide monomers are particularly preferred, and most preferably NVC.
  • the inkjet ink may also comprise one or more N-vinyl monomers other than an N-vinyl amide monomer and/or N-(meth)acryloyl amine monomer.
  • N-vinyl monomers other than an N-vinyl amide monomer and/or N-(meth)acryloyl amine monomer. Examples include N-vinyl carbazole, N-vinyl indole and N-vinyl imidazole.
  • the amount of monofunctional monomers present in the ink is restricted as monofunctional monomers are more prone to migration and odour issues, which is problematic for food packaging applications. Accordingly, in a preferred embodiment, the ink contains less than 5% by weight, more preferably less than 2% by weight, more preferably less than 1 % by weight and most preferably is substantially free of monofunctional monomer, where the amounts are based on the total weight of the ink.
  • substantially free is meant that only small amounts will be present, for example as impurities in the radiation-curable materials present or as a component in a commercially available pigment dispersion.
  • no monofunctional monomer is intentionally added to the ink.
  • minor amounts of monofunctional monomer which may be present as impurities in commercially available inkjet ink components, are tolerated.
  • the ink may comprise less than 0.5% by weight of monofunctional monomer, more preferably less than 0.1 % by weight of monofunctional monomer, most preferably less than 0.05% by weight of monofunctional monomer, based on the total weight of the ink.
  • the inkjet ink is free of monofunctional monomer.
  • the inkjet ink of the present invention may further comprise a radiation- curable (i.e. polymerisable) oligomer, such as a (meth)acrylate oligomer.
  • a radiation- curable (i.e. polymerisable) oligomer such as a (meth)acrylate oligomer.
  • Any radiation-curable oligomer that is compatible with the other ink components is suitable for use in the ink.
  • the inkjet ink comprises a (meth)acrylate oligomer.
  • 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 molecular weight of at least 600.
  • the molecular weight is preferably 4,000 or less.
  • Molecular weights (number average) can be calculated if the structure of the oligomer is known or molecular weights can be measured using gel permeation chromatography using polystyrene standards.
  • the oligomers may possess different degrees of functionality, and a mixture including combinations of mono, 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 preferably 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.
  • Oligomers are typically added to inkjet inks to increase the viscosity of the inkjet ink or to provide film-forming properties such as hardness or cure speed. 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 12° steel cone at 60°C with a shear rate of 25 s 1 .
  • 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 oligomers are (meth)acrylate oligomers.
  • the oligomer may include amine functionality, as the amine acts as an activator without the drawback of migration associated with low-molecular weight amines.
  • the radiation-curable oligomer is amine modified.
  • the radiation-curable oligomer is an amine- modified (meth)acrylate oligomer.
  • Particularly preferred radiation-curable oligomers are di-, tri-, tetra-, penta- or hexa-functional acrylates.
  • the radiation-curable oligomer is an amine-modified acrylate oligomer.
  • a suitable amine-modified polyester acrylate oligomer is commercially available as UVP6600.
  • a suitable amine-modified polyether acrylate oligomer is commercially available as CN3715LM.
  • 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.
  • epoxy based materials such as bisphenol A epoxy acrylates and epoxy novolac acrylates
  • the ink is preferably substantially free of bisphenol A based materials such as bisphenol A epoxy acrylates. Therefore, the ink is preferably substantially free of bisphenol A epoxy acrylates.
  • substantially free is meant that only small amounts will be present, for example as impurities in the radiation-curable materials present or as a component in a commercially available pigment dispersion.
  • no bisphenol A epoxy acrylates is intentionally added to the ink.
  • minor amounts of bisphenol A epoxy acrylates which may be present as impurities in commercially available inkjet ink components are tolerated.
  • the ink may comprise less than 0.5% by weight of bisphenol A epoxy acrylates, more preferably less than 0.1 % by weight of bisphenol A epoxy acrylates, most preferably less than 0.05% by weight of bisphenol A epoxy acrylates, based on the total weight of the ink.
  • the inkjet ink is free of bisphenol A epoxy acrylates.
  • the amount of radiation-curable oligomer, when present, is preferably 0.1-10% by weight, based on the total weight of the ink.
  • the inkjet ink of the present invention comprises a photoinitiator package, wherein the photoinitiator package comprises:
  • the inventors have surprisingly found that the inclusion of the photoinitiator package as claimed comprising the specific blend of photoinitiators in the specific amounts provides an inkjet ink that can be printed onto food packaging having low migration and odour, and which has a high UV LED cure speed and good surface cure. Higher molecular weight photoinitiators reduce migration and odour for food packaging applications.
  • This specific blend of photoinitiators surprisingly allows for efficient UV LED curing resulting in high UV LED cure speed and good surface cure.
  • the inkjet ink of the present invention comprises (i) 4.5 to 12.0% by weight of one or more polymeric a-aminoketone photoinitiators.
  • a polymeric a-aminoketone photoinitiator a photoinitiator comprising two or more a- aminoketone units connected by an a-aminoketone linking unit.
  • the a-aminoketone unit has the structure:
  • R 1 , R 2 , R 3 , R 4 and R 5 are not limited other than by the constraints imposed by the use in an ink-jet ink, such as viscosity, stability, toxicity etc.
  • R 1 , R 2 , R 3 , R 4 and R 5 are independently: hydrogen; C1-12 alkyl; C2-12 alkenyl; C2-12 alkynyl; C7-12 aralkyl; C7-12 alkaryl; C6-12 aryl; C5-12 heteroaryl; C2-C12 acylalkyl; oxygen, nitrogen or sulfur substituted with any of hydrogen, C1-12 alkyl, C2-12 alkenyl, C2-12 alkynyl, C7-12 aralkyl, C7-12 alkaryl, C6-12 aryl, C5-12 heteroaryl and/or C2-C12 acylalkyl; halogen; combinations thereof; the a-aminoketone linking unit; or two of R 1 , R 2 , R 3
  • R 1 is the a-aminoketone linking unit
  • R 2 and R 3 are independently C1-12 alkyl or C7- 12 alkaryl
  • R 4 and R 5 are independently C1-12 alkyl or together form a ring with 5 to 7 members optionally including oxygen or nitrogen.
  • R 1 is the a-aminoketone linking unit
  • R 2 and R 3 are independently methyl, ethyl or benzyl
  • R 4 and R 5 are methyl or together form a morpholine ring.
  • R 1 is the a-aminoketone linking unit
  • R 2 is ethyl
  • R 3 is benzyl
  • R 4 and R 5 are methyl.
  • R 1 is the a-aminoketone linking unit
  • R 2 and R 3 are methyl
  • R 4 and R 5 together form a morpholine ring.
  • the polymeric a-aminoketone photoinitiator has two or more a- aminoketone units.
  • the polymeric a-aminoketone photoinitiator has up to six a- aminoketone units.
  • the polymeric a-aminoketone photoinitiator has two to six a- aminoketone units, more preferably two to four a-aminoketone units.
  • the two or more a-aminoketone units may be the same or different but preferably they are the same.
  • the a-aminoketone linking unit is a polymer.
  • the polymer is not limited other than by the constraints imposed by the use in an ink-jet ink, such as viscosity, stability, toxicity etc.
  • the a-aminoketone linking unit has a core based on a polyhydroxy compound.
  • a polyhydroxy compound include ethylene glycol, propylene glycol, butylene glycol, glycerol, trimethylolpropane, di-trimethylolpropane, pentaerythritol and di-pentaerythritol.
  • the core based on a polyhydroxy compound is connected to the two or more a- aminoketone units by a phenylene linkage.
  • the phenylene linkage is not limited other than by the constraints imposed by the use in an ink-jet ink, such as viscosity, stability, toxicity etc.
  • the core based on a polyhydroxy compound is connected to the two or more a-aminoketone units by wherein * represents the point of attachment to the aminoketone unit, R 6 is oxygen, sulfur, NH, nitrogen substituted with C1-12 alkyl, C1-12 alkylene, C2-12 alkenylene, C2-12 alkynylene, C7-12 aralkylene, C7-12 alkarylene, C6-12 arylene, a disubstituted C4-12 heterocyclic ring, C2-C12 acylalkylene or combinations thereof, and the carbonyl carbon is connected to the core based on a polyhydroxy compound.
  • * represents the point of attachment to the aminoketone unit
  • R 6 is oxygen, sulfur, NH, nitrogen substituted with C1-12 alkyl, C1-12 alkylene, C2-12 alkenylene, C2-12 alkynylene, C7-12 aralkylene, C7-12 alkarylene, C6-12 arylene, a disubstitute
  • the core based on a polyhydroxy compound is connected to the two or more a- aminoketone units by wherein * represents the point of attachment to the aminoketone unit, R 6 is oxygen, sulfur, NH, nitrogen substituted with C1-12 alkyl, C1-12 alkylene, C2-12 alkenylene, C2-12 alkynylene, C7-12 aralkylene, C7-12 alkarylene, C6-12 arylene, a disubstituted C4-12 heterocyclic ring, C2-C12 acylalkylene or combinations thereof, and the carbonyl carbon is connected to the core based on a polyhydroxy compound.
  • * represents the point of attachment to the aminoketone unit
  • R 6 is oxygen, sulfur, NH, nitrogen substituted with C1-12 alkyl, C1-12 alkylene, C2-12 alkenylene, C2-12 alkynylene, C7-12 aralkylene, C7-12 alkarylene, C6-12 arylene, a disubstituted C
  • R 6 is oxygen, sulfur, NH, nitrogen substituted with C1-12 alkyl, C1-12 alkylene, a disubstituted C4-12 heterocyclic ring or combinations thereof. More preferably, R 6 is wherein nitrogen is connected to the phenylene carbon and CH2 is connected to the carbonyl carbon.
  • the a-aminoketone linking unit has the structure wherein R 6 is oxygen, sulfur, NH, nitrogen substituted with C1-12 alkyl, C1-12 alkylene, C2-12 alkenylene, C2-12 alkynylene, C7-12 aralkylene, C7-12 alkarylene, C6-12 arylene, a disubstituted C4-12 heterocyclic ring, C2-C12 acylalkylene or combinations thereof;
  • X is (OCH2CH2)nY, (OCH(CH 3 )CH 2 )nY, or (OCH2CH 2 CH 2 CH2)nY, wherein n is a value from 1 to 10 and Y is O, (CH2CH2CH2CH 2 O) n , wherein n is as defined above; and * represents the point of attachment to the a-aminoketone unit.
  • the a-aminoketone linking unit has the structure wherein R 6 is oxygen, sulfur, NH, nitrogen substituted with C1-12 alkyl, C1-12 alkylene, C2-12 alkenylene, C2-12 alkynylene, C7-12 aralkylene, C7-12 alkarylene, C6-12 arylene, a disubstituted C4-12 heterocyclic ring, C2-C12 acylalkylene or combinations thereof;
  • X is (OCH2CH2)nY, wherein W is C1-12 alkyl or C2-12 alkenyl, and Z is (CH2CH2O) n , (CH2CH(CH 3 )O) n , (CH2CH2CH2CH 2 O) n , wherein n is as defined above; and * represents the point of attachment to the a-aminoketone unit.
  • R 6 is oxygen, sulfur, NH, nitrogen substituted with C1-12 alkyl, C1-12 alkylene, a disubstituted C4-12 heterocyclic ring or combinations thereof. More preferably, R 6 is wherein nitrogen is connected to the phenylene carbon and CH2 is connected to the carbonyl carbon.
  • X is (OCH2CH2)nO, wherein n is a value from 1 to 10.
  • R 1 is the a-aminoketone linking unit
  • R 2 is ethyl
  • R 3 is benzyl
  • R 4 and R 5 are methyl
  • R 6 is wherein nitrogen is connected to the phenylene carbon and CH2 is connected to the carbonyl carbon
  • X is (OCH2CH2)nO, wherein n is a value from 1 to 10.
  • the one or more polymeric a-aminoketone photoinitiators have a molecular weight of more than 500 g/mol, more preferably more than 600 g/mol and most preferably more than 700 g/mol.
  • the one or more polymeric a-aminoketone photoinitiators have a molecular weight of less than 2000 g/mol, more preferably less than 1600 g/mol and most preferably less than 1200 g/mol.
  • the one or more polymeric a-aminoketone photoinitiators have a molecular weight of more than 500 g/mol to less than 2000 g/mol, more preferably more than 600 g/mol to less than 2000 g/mol and most preferably more than 700 g/mol to less than 2000 g/mol.
  • Molecular weights (number average) can be calculated if the structure of the photoinitiator is known or molecular weights can be measured using gel permeation chromatography using polystyrene standards.
  • the inkjet ink of the present invention comprises 4.5 to 12.0% by weight in total of one or more polymeric a-aminoketone photoinitiators, based on the total weight of the ink.
  • the inkjet ink comprises 5.5 to 10.0% by weight, more preferably 5.5 to 8.0% by weight, most preferably 5.5 to 7.5% by weight, in total of one or more polymeric a- aminoketone photoinitiators, based on the total weight of the ink.
  • the inventors have found that the presence of one or more polymeric a-aminoketone photoinitiators, particularly in the claimed amount, is required to provide high UV LED cure speed and good surface cure.
  • the inventors found that poor UV LED cure speed and surface cure is provided when this photoinitiator is absent and reduced cure speed is provided when there is a reduced amount of this photoinitiator present.
  • This photoinitiator is also suitable for food packaging, having a high molecular weight, resulting in reduced migration and odour issues.
  • the polymeric a-aminoketone photoinitiator may be used alone or two or more polymeric a- aminoketone photoinitiators may be used together.
  • suitable polymeric a-aminoketone photoinitiators include Omnipol 910 from IGM.
  • the one or more polymeric a-aminoketone photoinitiators comprise wherein n is a value from 1 to 10, based on the total weight of the ink.
  • n is a value from 1 to 10, based on the total weight of the ink., is a piparazino based aminoalkylphenone.
  • n is a value from 1 -5, more preferably 2-4.
  • This photoinitiator is commercially available as Omnipol 910 from IGM with the CAS number 886463-10-1. It is also commercially available as Omnipol 9210 from IGM containing 80% Omnipol 910 in 20% pentaerythritol [5 EO] tetraacrylate (PPTTA).
  • this photoinitiator is present in 4.5 to 12.0% by weight, more preferably 5.5 to 10.0% by weight, more preferably 5.5 to 8.0% by weight, most preferably 5.5 to 7.5% by weight, based on the total weight of the ink.
  • Omnipol 9210 is the only polymeric a-aminoketone photoinitiator used, it is the total amount of photoinitiator (Omnipol 910) that is present in the ink in 4.5 to 12.0% by weight, based on the total weight of the ink.
  • the inventors have found that the presence of Omnipol 910 in the photoinitiator package of the ink, in the claimed amount, is particularly beneficial in providing high UV LED cure speed and good surface cure.
  • Omnipol 910 is also suitable for food packaging, having a high molecular weight, resulting in reduced migration and odour issues.
  • the inkjet ink of the present invention comprises (ii) 1 .5 to 5.0% by weight in total of one or more polymeric thioxanthone photoinitiators, based on the total weight of the ink.
  • a polymeric thioxanthone photoinitiator is meant a photoinitiator comprising two or more thioxanthone units connected by a thioxanthone linking unit.
  • the thioxanthone unit has the structure:
  • R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are not limited other than by the constraints imposed by the use in an ink-jet ink, such as viscosity, stability, toxicity etc.
  • R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are independently hydrogen, halogen, C1-12 alkyl, C2-12 alkenyl, C2-12 alkynyl, C7-12 aralkyl, C7-12 alkaryl, C6-12 aryl, C5-12 heteroaryl or the thioxanthone linking unit, with the proviso that one of R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 is the thioxanthone linking unit.
  • R 2 is hydrogen or halogen
  • R 1 , R 3 , R 4 , R 5 and R 7 are hydrogen
  • R 6 and R 8 are independently hydrogen or the thioxanthone linking unit, with the proviso that one of R 6 and R 8 is the thioxanthone linking unit.
  • R 2 is hydrogen or chlorine
  • R 1 , R 3 , R 4 , R 5 and R 7 are hydrogen
  • R 6 and R 8 are independently hydrogen or the thioxanthone linking unit, with the proviso that one of R 6 and R 8 is the thioxanthone linking unit.
  • R 1 , R 2 , R 3 , R 4 , R 5 , R 7 and R 8 are hydrogen and R 6 is the thioxanthone linking unit.
  • R 2 is chlorine
  • R 1 , R 3 , R 4 , R 5 , R 6 and R 7 are hydrogen
  • R 8 is the thioxanthone linking unit.
  • the polymeric thioxanthone photoinitiator has three or more thioxanthone units, more preferably four or more thioxanthone units.
  • the polymeric thioxanthone photoinitiator has up to six thioxanthone units.
  • the polymeric thioxanthone photoinitiator has two to six thioxanthone units, more preferably two to four thioxanthone units.
  • the two or more thioxanthone units may be the same or different but preferably they are the same.
  • the thioxanthone linking unit is a polymer.
  • the polymer is not limited other than by the constraints imposed by the use in an ink-jet ink, such as viscosity, stability, toxicity etc.
  • the thioxanthone linking unit has a core based on a polyhydroxy compound.
  • a polyhydroxy compound include ethylene glycol, propylene glycol, butylene glycol, glycerol, trimethylolpropane, di-trimethylolpropane, pentaerythritol and di-pentaerythritol.
  • W is C1-10 alkylene or C2-10 alkenylene, more preferably C1-6 alkylene or C2-6 alkenylene. More preferably, W is (CH) m R 9 wherein m is a value from 1 to 6 and R 9 is hydrogen, CH3 or CH2CH3. Most preferably, W is CH2.
  • the repeating monomer unit is not limited other than by the constraints imposed by the use in an ink-jet ink, such as viscosity, stability, toxicity etc.
  • Non-limiting examples include (OCH2CH2)n, (OCH(CH3)CH 2 )n, or (OCH2CH2CH2CH2)n, wherein n is a value from 1 to 10.
  • W is C1-10 alkylene or C2-10 alkenylene, more preferably Ci-e alkylene or C 2 -e alkenylene. More preferably, W is (CH) m R 9 wherein m is a value from 1 to 6 and R 9 is hydrogen, CH 3 or CH 2 CH 3 . Most preferably, W is CH 2 .
  • X is (OCH 2 CH 2 CH 2 CH 2 ) n O, wherein n is a value from 1 to 10.
  • R 1 , R 2 , R 3 , R 4 , R 5 , R 7 and R 8 are hydrogen
  • R 6 is the thioxanthone linking unit
  • W is CH 2
  • X is (OCH 2 CH 2 CH 2 CH 2 ) n O, wherein n is a value from 1 to 10.
  • n is a value from 1 to 10 and * represents the point of attachment to the thioxanthone unit.
  • the value of n in total in X is preferably a value from 1 to 20, more preferably from 1 to 15.
  • R 2 is chlorine
  • R 1 , R 3 , R 4 , R 5 , R 6 and R 7 are hydrogen
  • R 8 is the thioxanthone linking unit
  • R 2 is chlorine
  • R 1 , R 3 , R 4 , R 5 , R 6 and R 7 are hydrogen
  • R 8 is the thioxanthone linking unit
  • W is CH 2
  • n is a value from 1 to 10 and * represents the point of attachment to the thioxanthone unit.
  • the value of n in total in X is preferably a value from 1 to 20, more preferably from 1 to 15.
  • the one or more polymeric thioxanthone photoinitiators have a molecular weight of more than 500 g/mol, more preferably more than 600 g/mol and most preferably more than 700 g/mol.
  • the one or more polymeric thioxanthone photoinitiators have a molecular weight of less than 2000 g/mol, more preferably less than 1500 g/mol and most preferably less than 1000 g/mol.
  • the one or more polymeric thioxanthone photoinitiators have a molecular weight of more than 500 g/mol to less than 2000 g/mol, more preferably more than 600 g/mol to less than 2000 g/mol and most preferably more than 700 g/mol to less than 2000 g/mol.
  • Molecular weights (number average) can be calculated if the structure of the photoinitiator is known or molecular weights can be measured using gel permeation chromatography using polystyrene standards.
  • the inkjet ink of the present invention comprises 1 .5 to 5.0% by weight in total of one or more polymeric thioxanthone photoinitiators, based on the total weight of the ink.
  • the inkjet ink comprises 2.0 to 4.0% by weight in total of one or more polymeric thioxanthone photoinitiators, based on the total weight of the ink.
  • the inventors have found that the presence of one or more polymeric thioxanthone photoinitiators, in the claimed amount, is required to provide high UV LED cure speed and good surface cure.
  • the inventors found that poor UV LED cure speed and surface cure is provided when this photoinitiator is absent and reduced cure speed is provided when there is a reduced amount of this photoinitiator present.
  • This photoinitiator is also suitable for food packaging, having a high molecular weight, resulting in reduced migration and odour issues.
  • the polymeric thioxanthone photoinitiator may be used alone or two or more polymeric thioxanthone photoinitiators may be used together.
  • suitable polymeric thioxanthone photoinitiators include Speedcure 7010 from Lambson, Omnipol TX from IGM, Genopol TX-2 from Rahn and JRCure 1508 from Jiuri.
  • the one or more polymeric thioxanthone photoinitiators comprise wherein a+b+c+d is a value from 1 to 20, and/or
  • q is a value from 1 to 10.
  • the photoinitiator wherein a+b+c+d is a value from 1 to 20, is 1 ,3-di( ⁇ a-[1-chloro-9-oxo-9H-thioxanthen-4- yl)oxy]acetylpoly[oxy(1 -methylethylene)] ⁇ oxy)-2,2-bis( ⁇ a-[1 -chloro-9-oxo-9H-thioxanthen-4- yl)oxy]acetylpoly[oxy(1-methylethylene)] ⁇ oxymethyl) propane.
  • This photoinitiator is commercially available as Speedcure 7010 from Lambson. It is also commercially available as Speedcure 7010L from Lambson containing 40% Speedcure 7010 in 60% trimethylolpropane ethoxylate triacrylate.
  • Speedcure 7010 has the CAS number 1003567-83-6 and trimethylolpropane ethoxylate triacrylate has the CAS number 28961-43-5.
  • the value of a+b+c+d in the chemical formula of Speedcure 7010 is equal to 1 to 20. In a preferred embodiment, the value of a+b+c+d in the chemical formula of Speedcure 7010 is equal to 1 to 15.
  • the photoinitiator wherein q is a value from 1 to 10, is a photoinitiator having two repeating thioxanthone monomer units. It is commercially available as Omnipol TX from IGM, with a molecular weight of 790 g/mol and with CAS number 813452-37-8. It is also commercially available as Genopol TX-2 from Rahn, with a molecular weight of 980 g/mol.
  • the inkjet ink comprises a radiation-curable material and a photoinitiator package, wherein the photoinitiator package comprises:
  • a+b+c+d is a value from 1 to 20, and/or wherein q is a value from 1 to 10;
  • the inkjet ink of the present invention preferably comprises (ii) 1 .5 to 5.0% by weight in total of at least one of Speedcure 7010, Omnipol TX and/or Genopol TX-2, based on the total weight of the ink.
  • the inkjet ink may comprise: Speedcure 7010; Omnipol TX; Genopol TX-2; Speedcure 7010 and Omnipol TX; Speedcure 7010 and Genopol TX-2; Omnipol TX and Genopol TX-2; or Speedcure 7010, Omnipol TX and Genopol TX-2.
  • the total amount of at least one of Speedcure 7010, Omnipol TX and/or Genopol TX-2 in the inkjet ink in combination is preferably 1 .5 to 5.0% by weight, based on the total weight of the ink.
  • the inkjet ink comprises (ii) 1 .5 to 5.0% by weight, preferably 2.0 to 4.0% by weight of Speedcure 7010, based on the total weight of the ink.
  • the inkjet ink comprises (ii) 1 .5 to 5.0% by weight, preferably 2.0 to 4.0% by weight of Omnipol TX, based on the total weight of the ink.
  • the inkjet ink comprises (ii) 1 .5 to 5.0% by weight, preferably 2.0 to 4.0% by weight of Genopol TX-2, based on the total weight of the ink.
  • the inkjet ink comprises (ii) 1 .5 to 5.0% by weight in total, preferably 2.0 to 4.0% by weight in total of Speedcure 7010 and Omnipol TX, based on the total weight of the ink.
  • the inkjet ink comprises (ii) 1 .5 to 5.0% by weight in total, preferably 2.0 to 4.0% by weight in total of Speedcure 7010 and Genopol TX-2, based on the total weight of the ink.
  • the inkjet ink comprises (ii) 1 .5 to 5.0% by weight in total, preferably 2.0 to 4.0% by weight in total of Omnipol TX and Genopol TX-2, based on the total weight of the ink.
  • the inkjet ink comprises (ii) 1 .5 to 5.0% by weight in total, preferably 2.0 to 4.0% by weight in total of Speedcure 7010, Omnipol TX and Genopol TX-2, based on the total weight of the ink.
  • Speedcure 7010L it is the total amount of photoinitiator (Speedcure 7010) that is relevant when assessing the total amount of Speedcure 7010 present in the ink.
  • the photoinitiator package comprises (ii) 2.0 to 4.0% by weight in total of
  • a+b+c+d is a value from 1 to 20, and/or wherein q is a value from 1 to 10, based on the total weight of the ink.
  • Speedcure 7010, Omnipol TX and/or Genopol TX-2 are particularly beneficial in providing high UV LED cure speed and good surface cure.
  • Speedcure 7010, Omnipol TX and Genopol TX-2 are also suitable for food packaging, having a high molecular weight, resulting in reduced migration and odour issues.
  • the inkjet ink of the present invention comprises 1 .0 to 5.0% by weight, preferably 3.0 to 4.5% by weight, of: based on the total weight of the ink.
  • This photoinitiator is phenyl bis(2,4,6-trimethylbenzoyl)- phosphine oxide and is known as BAPO. It is commercially available as Omnirad 819 from IGM with CAS number 162881-26-7.
  • the photoinitiator package comprises (iii) 3.0 to 4.5% by weight of based on the total weight of the ink.
  • the inventors have found that the presence of BAPO in the photoinitiator package of the ink, in the claimed amount, is required to provide high UV LED cure speed and good surface cure.
  • the inventors found that poor UV LED cure speed and surface cure is provided when this photoinitiator is absent and reduced cure speed is provided when there is a reduced amount of this photoinitiator present.
  • the photoinitiator package comprises one or more additional photoinitiators.
  • an additional photoinitiator is meant a photoinitiator other than Omnipol 819, the one or more polymeric thioxanthone photoinitiators and the one or more polymeric a-aminoketone photoinitiators.
  • the one or more additional photoinitiators are not particularly limited.
  • Preferred one or more additional photoinitiators are photoinitiators which produce free radicals on irradiation (free radical photoinitiators) such as, for example, benzophenone, 1 -hydroxycyclohexyl phenyl ketone, 2-benzyl-2-dimethylamino-(4-morpholinophenyl)butan-1-one, benzil dimethylketal, phenylbis(2,4,6-trimethylbenzoyl) phosphine oxide, ethyl(2,4,6-trimethylbenzoyl)-phenyl phosphinate (TPO-L), diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide (TPO), 1-[4-(2- hydroxyethoxyl)-phenyl]-2-hydroxy-2-methylpropanone (Omnirad 2959), 2-hydroxy-1-[4-[4-(2- hydroxy-2-methylpropanoyl)phenoxy]phenyl]-2-methylprop
  • the photoinitiator package of the ink of the present invention further comprises two or more additional photoinitiators.
  • the photoinitiator package of the ink of the present invention contains up to five photoinitiators.
  • the photoinitiator package is present in the ink in 7-30% by weight, more preferably 10-25% by weight, and most preferably 12-18% by weight, based on the total weight of the ink.
  • the inkjet ink preferably contains less than 5% by weight, more preferably less than 2% by weight, more preferably less than 1 % by weight, and more preferably is substantially free of any additional photoinitiators.
  • the ink is therefore preferably substantially free of any photoinitiators, other than Omnipol 819, the one or more polymeric thioxanthone photoinitiators and the one or more polymeric a-aminoketone photoinitiators.
  • Omnipol 819, the one or more polymeric thioxanthone photoinitiators and the one or more polymeric a-aminoketone photoinitiators are the only photoinitiators present in the inkjet ink.
  • substantially free is meant that only small amounts will be present, for example as impurities in the radiation-curable materials present.
  • no additional photoinitiator is intentionally added to the ink.
  • minor amounts of additional photoinitiator which may be present as impurities in commercially available inkjet ink components, are tolerated.
  • the ink may comprise less than 0.5% by weight of additional photoinitiator, more preferably less than 0.1 % by weight of additional photoinitiator, most preferably less than 0.05% by weight of additional photoinitiator, based on the total weight of the ink.
  • the inkjet ink is free of additional photoinitiator.
  • the photoinitiator package consists of:
  • the photoinitiator package consists of:
  • n is a value from 1 to 10;
  • the ink may also contain a resin.
  • the resin preferably has a weight-average molecular weight (Mw) of 20-200 KDa, and most preferably 20-60 KDa.
  • Mw may be measured by known techniques in the art, such as gel permeation chromatography (GPC), using a polystyrene standard.
  • the resin is preferably solid at 25°C. It is preferably soluble in the liquid medium of the ink (the radiation-curable material and, when present, additionally the solvent).
  • the resin is a passive (i.e. inert) resin, in the sense that it is not radiation curable and hence does not undergo cross-linking under the curing conditions to which the ink is subjected.
  • the resin may improve adhesion of the ink to the substrate. It is preferably soluble in the ink.
  • the resin, when present, is preferably present at 0.1-5% by weight, based on the total weight of the ink.
  • the inkjet ink of the present invention also includes a colouring agent, which may be either dissolved or dispersed in the liquid medium of the ink.
  • a colouring agent can be any of a wide range of suitable colouring agents that would be known to the person skilled in the art.
  • the colouring agent is a 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 13, Pigment Yellow 83, Pigment Red 9, Pigment Red 184, Pigment Blue 15:3, Pigment Green 7, Pigment Violet 19, Pigment Black 7.
  • black and the colours required for trichromatic process printing may be used.
  • 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 pm, preferably less than 5 pm, more preferably less than 1 pm and particularly preferably less than 0.5 pm.
  • the colorant is preferably present in an amount of 0.2-20% by weight, preferably 0.5-15% by weight, based on the total weight of the ink.
  • a higher concentration of pigment may be required for white inks, for example up to and including 30% by weight, or 25% by weight, based on the total weight of the ink.
  • the inkjet ink preferably dries primarily by curing, i.e. by the polymerisation of the monomers present, as discussed hereinabove, and hence is a curable ink.
  • the ink does not, therefore, require the presence of water or a volatile organic solvent to effect drying of the ink.
  • the inkjet ink comprises less than 5% by weight of water and volatile organic solvent combined, preferably less than 3% by weight combined, more preferably, less than 2% by weight combined and more preferably less than 1 % by weight combined, and most preferably, the inkjet ink is substantially free of water and volatile organic solvents, where the amounts are based on the total weight of the ink.
  • substantially free is meant that only small amounts will be present, for example some water will typically be absorbed by the ink from the air and solvents may be present as impurities in the components of the inks, but such low levels are tolerated. In other words, no water or a volatile organic solvent is intentionally added to the ink. However, minor amounts of water or a volatile organic solvent, which may be present as impurities in commercially available inkjet ink components, are tolerated.
  • the ink may comprise less than 0.5% by weight of water or a volatile organic solvent, more preferably less than 0.1 % by weight of water or a volatile organic solvent, most preferably less than 0.05% by weight of water or a volatile organic solvent, based on the total weight of the ink. In a preferred embodiment, the inkjet ink is free of water or a volatile organic solvent.
  • the inkjet ink comprises a surfactant.
  • the surfactant controls the surface tension of the ink.
  • Surfactants are well known in the art and a detailed description is not required.
  • An example of a suitable surfactant is BYK307. Adjustment of the surface tension of the inks allows control of the surface wetting of the inks on various substrates, for example, plastic substrates. Too high a surface tension can lead to ink pooling and/or a mottled appearance in high coverage areas of the print. Too low a surface tension can lead to excessive ink bleed between different coloured inks. Surface tension is also critical to ensuring stable jetting (nozzle plate wetting and sustainability).
  • the surface tension is preferably in the range of 18-40 mNm 1 , more preferably 20-35 mNnr 1 and most preferably 20-30 mNnr 1 .
  • components of types known in the art may be present in the ink of the present invention to improve the properties or performance.
  • these components may be, for example, additional surfactants, defoamers, dispersants, synergists, stabilisers against deterioration by heat or light other than an aerobic stabiliser, reodorants, flow or slip aids, biocides and identifying tracers.
  • the amounts by weight provided herein are based on the total weight of the ink.
  • the ink or inkjet ink sets may be prepared by known methods such as stirring with a high-speed water-cooled stirrer, or milling on a horizontal bead-mill.
  • the ink exhibits a desirable low viscosity, less than 100 mPas, preferably 50 mPas or less, more preferably 30 mPas or less and most preferably 20 mPas or less at 25°C.
  • the ink most preferably has a viscosity of 8 to 20 mPas at 25°C. Viscosity may be measured using a digital Brookfield viscometer fitted with a thermostatically controlled cup and spindle arrangement, such as model DV1.
  • the present invention also provides an inkjet ink set, wherein the inkjet ink set of the invention has at least one ink that falls within the scope of the inkjet ink according to the present invention. Preferably, all of the inks in the set fall within the scope of the inkjet ink according to the present invention.
  • the inkjet ink set of the present invention is 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).
  • This set is often termed CMYK.
  • the inks in a trichromatic set can be used to produce a wide range of colours and tones.
  • the present invention also provides a method of inkjet printing comprising inkjet printing the inkjet ink as defined herein onto a substrate and curing the inkjet ink by exposing the inkjet ink to a curing source.
  • the inkjet ink is inkjet printed onto a substrate.
  • Printing is performed by inkjet printing, e.g. on a single-pass inkjet printer, for example for printing (directly) onto a substrate, on a roll-to-roll printer or a flat-bed printer.
  • inkjet printing is well known in the art and a detailed description is not required.
  • the ink is jetted from one or more reservoirs or printing heads through narrow nozzles on to a substrate to form a printed image.
  • Print heads account for a significant portion of the cost of an entry level printer and it is therefore desirable to keep the number of print heads (and therefore the number of inks in the ink set) low. Reducing the number of print heads can reduce print quality and productivity. It is therefore desirable to balance the number of print heads in order to minimise cost without compromising print quality and productivity.
  • Substrates include those for packaging applications and in particular, flexible packaging applications. Examples include substrates composed of polyvinyl chloride (PVC), polystyrene, polyester, polyethylene terephthalate (PET), polyethylene terephthalate glycol modified (PETG) and polyolefin (e.g. polyethylene, polypropylene or mixtures or copolymers thereof). Further substrates include all cellulosic materials such as paper and board, or their mixtures/blends with the aforementioned synthetic materials.
  • PVC polyvinyl chloride
  • PET polyethylene terephthalate
  • PETG polyethylene terephthalate glycol modified
  • polyolefin e.g. polyethylene, polypropylene or mixtures or copolymers thereof.
  • Further substrates include all cellulosic materials such as paper and board, or their mixtures/blends with the aforementioned synthetic materials.
  • Particularly preferred substrates are a food packaging.
  • Food packaging is typically formed of flexible and rigid plastics (e.g. food-grade polystyrene and PE/PP films), paper and board (e.g. corrugated board).
  • Printing onto a food packaging substrate represents a particular challenge on account of the strict safety limitations on the properties of materials which come into contact with food, including indirect additives like packaging inks.
  • Specific exclusions based on their odour and/or migration properties include volatile organic solvents and many monomers typically used in UV curing inks.
  • the monomers present in the ink of the present invention are suitable for food packaging applications.
  • the surface which is most important since it is the surface which is wetted by the ink.
  • the surface of substrate is composed of the abovediscussed material.
  • the substrate is a laminate carton material comprising the following layers, in order: an inner polyethylene layer; an aluminium layer; a board layer; and an outer polyethylene layer.
  • inner is meant a surface of the substrate that would come into contact with food
  • outer is meant a surface of the substrate that would come into contact with the inkjet ink used in the method of the present invention.
  • the polyethylene layer is corona treated to a surface tension of more than 45 dynes/cm using a Vetaphone unit. This provides improved adhesion of the ink.
  • the present invention may also provide a printed substrate having the ink as defined herein printed thereon.
  • the substrate is a food packaging.
  • the inkjet ink is jetted at drop sizes below 90 picolitres, preferably below 35 picolitres and most preferably below 10 picolitres.
  • a low viscosity ink is required.
  • a viscosity of 30 mPas or less at 25°C is preferred, for example, 8 to 12 mPas, 18 to 20 mPas, or 24 to 26 mPas.
  • Ink viscosity may be measured using a Brookfield viscometer fitted with a thermostatically controlled cup and spindle arrangement, such as a DV1 low-viscosity viscometer running at 20 rpm at 25°C with spindle 00.
  • the ink of the present invention is cured by any means known in the art, such as exposure to actinic radiation and low-energy electron beam radiation.
  • drying and “cure” are often used interchangeably in the art when referring to radiation-curable inkjet inks to mean the conversion of the inkjet ink from a liquid to solid by polymerisation and/or crosslinking of the radiation-curable material.
  • drying is meant the removal of the water by evaporation
  • curing is meant the polymerisation and/or crosslinking of the radiation-curable material. Further details of the printing, drying and curing process are provided in WO 2011/021052.
  • the ink is cured by exposing the printed ink to a source of 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 are well known in the art and a detailed description is not required. These include mercury discharge lamps, fluorescent tubes, light emitting diodes (LEDs), flash lamps and combinations thereof
  • the source of actinic radiation is a mercury discharge lamp and/or LEDs.
  • the inventors have found that the inkjet ink has improved surface cure and cure speed when the source of actinic radiation is a mercury discharge lamp or LEDs
  • the source of actinic radiation is LEDs.
  • the ink of the present invention comprising the particular photoinitiator package having the specific blend of photoinitiators in the specific amounts allows for increased cure speed and improved surface cure when curing with a UV LED curing source. It is particularly challenging to provide improved surface cure and a high cure speed when curing with a UV LED curing source. This is even more challenging when the formulator’s choice of ink components is restricted when providing inkjet inks for food packaging.
  • the present inventors have been able to prepare an inkjet ink that is suitable for food packaging and which also obtains improved surface cure and cure speed by providing the specific photoinitiator package as claimed.
  • LEDs are increasingly used to cure inkjet inks. UV light is emitted from a UV LED light source. UV LED light sources comprise one or more LEDs and are well known in the art. Thus, a detailed description is not required.
  • UV LED light sources emit radiation having a spread of wavelengths.
  • the emission of UV LED light sources is identified by the wavelength which corresponds to the peak in the wavelength distribution.
  • UV LED light sources emit UV radiation over a narrow range of wavelengths on the wavelength distribution.
  • the width of the range of wavelengths on the wavelength distribution is called a wavelength band. LEDs therefore have a narrow wavelength output when compared to other sources of UV radiation.
  • a narrow wavelength band it is meant that at least 90%, preferably at least 95%, of the radiation emitted from the UV LED light source has a wavelength within a wavelength band having a width of 50 nm or less, preferably, 30 nm or less, most preferably 15 nm or less.
  • At least 90%, preferably at least 95%, of the radiation emitted from the UV LED light source has a wavelength in a band having a width of 50 nm or less, preferably 30 nm or less, most preferably 15 nm or less.
  • LEDs have a longer lifetime and exhibit no change in the power/wavelength output overtime. LEDs also have the advantage of switching on instantaneously with no thermal stabilisation time and their use results in minimal heating of the substrate.
  • the ink may also be cured by exposing the printed ink to low-energy electron beam (ebeam).
  • ebeam low-energy electron beam
  • the source of low-energy electron beam can be any source of low-energy electron beam that is suitable for curing radiation-curable inks.
  • Suitable low-energy electron beam radiation sources include commercially available ebeam curing units, such as the EB Lab from ebeam Technologies with energy of 80-300 keV and capable of delivering a typical dose of 30-50 kGy at line speeds of up to 30 m/min.
  • low-energy forthe ebeam, it is meant that it delivers an electron beam having a dose at the substrate of 100 kGy or less, preferably 70 kGy or less.
  • Ebeam curing is characterised by dose (energy per unit mass, measured in kilograys (kGy)) deposited in the substrate via electrons. Electron beam surface penetration depends upon the mass, density and thickness of the material being cured. Compared with UV penetration, electrons penetrate deeply through both lower and higher density materials. Unlike UV curing, photoinitiators are not required for ebeam curing to take place.
  • Ebeam curing is well-known in the art and therefore a detailed explanation of the curing method is not required.
  • the ink of the invention is exposed to the ebeam, which produces sufficient energy to instantaneously break chemical bonds and enable polymerisation or crosslinking.
  • the dose is more than 10 kGy, more preferably more than 20 kGy, more preferably more than 30 kGy and most preferably more than 40 kGy.
  • the dose is less than 100 kGy, more preferably less than 90 kGy, more preferably less than 80 kGy and most preferably less than 70 kGy.
  • the dose is more than 30 kGy but less than 70 kGy, more preferably more than 30 kGy but less than 60 kGy and most preferably, more than 30 kGy but 50 kGy or less. Doses above 50 kGy may cause damage to the substrate, particularly the substrates used for food packaging applications, and so doses of 50 kGy or less are preferred.
  • the energy associated with these doses is 80-300 keV, more preferably 70-200 keV and most preferably 100 keV.
  • the ink cures to form a relatively thin polymerised film.
  • the ink of the present invention typically produces a printed film having a thickness of 1 to 20 pm, preferably 1 to 10 pm, for example 2 to 5 pm. Film thicknesses can be measured using a confocal laser scanning microscope.
  • Inkjet inks were prepared according to the formulations set out in Table 1.
  • the inkjet ink formulations were prepared by mixing the components in the given amounts. Amounts are given as weight percentages based on the total weight of the ink.
  • Inks A-H have varying amounts of Speedcure 7010L and Omnipol 9210.
  • Inks F and H are examples of the invention as they have the claimed photoinitiator package comprising the claimed photoinitiators in the claimed amounts.
  • Inks A-E and G are comparative examples.
  • comparative inks A and C do not comprise Speedcure 7010L.
  • Comparative ink A also does not have the required amount of Omnipol 9210.
  • Comparative inks B and D do not comprise Omnipol 9210.
  • Comparative inks E and G do not have the required amount of Omnipol 9210.
  • the cyan pigment dispersion contains 30% pigment, 20% polymeric dispersing aid and 50% DVE- 3.
  • the dispersion was prepared by mixing the components in the given amounts and passing the mixture through a bead mill until the dispersion had a particle size of less than 0.3 microns. Amounts are given as weight percentages based on the total weight of the dispersion.
  • the viscosity of the ink was measured using a Brookfield viscometer running at 30 rpm at 25°C. All of the inkjet inks have a viscosity of less than 20 mPa.s and so have an ink-jettable viscosity. Surface cure at varying cure speed
  • the inks were drawn down in a 12 pm film using a 12 pm wire wound K-bar onto a PP60 Top White substrate available from Avery Demnison.
  • the 12 pm drawdowns were then passed under a 20W, 395 nm LED UV light (Phoseon Firepower FP300 150 x 20 mm) at varying belt speeds to provide a cured ink film.
  • the cured ink film had a piece of Epson photo paper placed face down on the cured ink film. The back of the photo paper was rubbed by hand in both direction 10 times. The photo paper was then pulled away from the cured ink film.
  • the photo paper will separate with no offset and no noise. If the film is not fully cured and has poor surface cure, the ink will offset to the photo paper and/or noise is observed as force is required to separate the partially cured ink film and the photo paper.
  • Example inks F and H have improved surface cure and cure speed when compared to comparative inks A-E and G.
  • comparative Ink C contains the same amount of Omnipol 9210 and Omnirad 819, but Speedcure 7010L is notably absent from comparative Ink C.
  • Inks F and H have improved UV LED cure at various belt speeds, when compared to comparative Ink C. This shows that the presence of Speedcure 7010L is required to provide improved surface cure and high cure speed.
  • comparative ink D contains the same amount of Speedcure 7010L and Omnirad 819, but Omnipol 9210 is notably absent from comparative Ink D.
  • Ink F has improved UV LED cure at various belt speeds, when compared to comparative Ink D. This shows that the presence of Omnipol 9210 is required to provide improved surface cure and high cure speed.
  • a similar comparison can be made between Ink H of the invention and comparative Ink B and similar results are obtained.
  • comparative Ink G has the same amount of Speedcure 7010L and Omnirad 819, but Omnipol 9210 is not present in the required amount in comparative Ink G.
  • Ink F again has improved cure at various belt speeds, when compared to comparative Ink G. This shows that the claimed amount of Omnirad 9210 is required to provide improved surface cure and high cure speed.
  • Ink H of the invention has improved surface cure and cure speed when compared to ink H owing to the increased amount of Speedcure 7010L and Ink F is the most preferred example of the invention.
  • Inkjet inks were prepared according to the formulations set out in Table 4.
  • the inkjet ink formulations were prepared by mixing the components in the given amounts. Amounts are given as weight percentages based on the total weight of the ink.
  • Inks l-L and F have varying amounts of BAPO, whilst maintaining the amount of Speedcure 7010L and Omnipol 9210.
  • Inks J-L and F are examples of the invention as they have the claimed photoinitiator package comprising the claimed photoinitiators in the claimed amounts.
  • Ink I is a comparative example as it does not comprise BAPO.
  • the cyan pigment dispersion is as detailed for Example 1 .
  • Example inks J-L and F have improved cure speed when compared to comparative ink I. It is apparent from these cure results that BAPO is required in the photoinitiator package in order to provide improved UV LED surface cure and cure speed.
  • comparative ink I does not comprise BAPO and has a cure score of 1 for all belt speeds.
  • BAPO ink J
  • improved cure can be seen at a belt speed of 25 m/min when compared to an ink (ink I), which does not comprise BAPO.
  • Improved cure results can be seen as the amount of BAPO is increased, and is exemplified in ink F.
  • Inkjet inks were prepared according to the formulations set out in Table 6.
  • the inkjet ink formulations were prepared by mixing the components in the given amounts. Amounts are given as weight percentages based on the total weight of the ink.
  • the cyan pigment dispersion is as detailed for Example 1.
  • the magenta pigment dispersion contains 30% pigment, 42% polymeric dispersing aid and 28% DVE-3.
  • the yellow pigment dispersion contains 20% pigment, 10% polymeric dispersing aid, 1 % stabiliser and 69% 3MPDA.
  • the black pigment dispersion contains 40% pigment, 20% polymeric dispersing aid, 0.9% synergist and 39.1 % DVE-3.
  • the dispersions were prepared by mixing the components in the given amounts and passing the mixture through a bead mill until the dispersion had a particle size of less than 0.3 microns. Amounts are given as weight percentages based on the total weight of the dispersion.
  • Inks M-P is an inkjet ink set of the present invention comprising CMYK inks of the invention.
  • the inks are examples of the invention as they have the claimed photoinitiator package comprising the claimed photoinitiators in the claimed amounts.
  • Table 8 Tables 7 and 8 show that improved UV LED surface cure and fast cure speed can be achieved when using various cure sources, including a 16 W 40 mm LED lamp and a mercury UV lamp system.

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Ink Jet Recording Methods And Recording Media Thereof (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)

Abstract

La présente invention concerne une encre pour impression à jet d'encre comprenant un matériau durcissable par rayonnement et un emballage de photoinitiateur, l'emballage de photoinitiateur comprenant : (i) 4,5 à 12,0 % en poids d'un ou de plusieurs photoinitiateurs d'α-aminocétones polymères ; (ii) 1,5 à 5,0 % en poids au total d'un ou de plusieurs photo-initiateurs de thioxanthone polymères ; et (iii) 1,0 à 5,0 % en poids de (formule) ; les quantités étant basées sur le poids total de l'encre. La présente invention concerne également un procédé d'impression de l'encre pour impression à jet d'encre de la présente invention.
PCT/GB2021/052796 2020-10-29 2021-10-28 Encre d'impression WO2022090718A1 (fr)

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GB2017159.1 2020-10-29
GBGB2017159.1A GB202017159D0 (en) 2020-10-29 2020-10-29 Printing ink
GBGB2017869.5A GB202017869D0 (en) 2020-11-12 2020-11-12 Printing ink
GB2017869.5 2020-11-12
GBGB2109028.7A GB202109028D0 (en) 2021-06-23 2021-06-23 Printing ink
GB2109028.7 2021-06-23

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115044282A (zh) * 2022-08-17 2022-09-13 佛山市儒林化工有限公司 一种食品罐外用安全叠压无迁移uv光油及其制备方法
EP4056658A1 (fr) * 2021-03-12 2022-09-14 Marabu GmbH & Co. KG Composition durcissable par exposition à un rayonnement

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WO2011021052A2 (fr) 2009-08-21 2011-02-24 Sericol Limited Encre, appareil et procédé d'impression
EP2832553A1 (fr) * 2012-03-30 2015-02-04 FUJIFILM Corporation Procédé d'enregistrement par jet d'encre et matière imprimée
WO2016178989A1 (fr) * 2015-05-01 2016-11-10 Sun Chemical Corporation Composition d'encre ou de revêtement durcissable par de l'énergie et électriquement isolante
JP2017105902A (ja) * 2015-12-08 2017-06-15 コニカミノルタ株式会社 活性光線硬化型インクジェットインク及び画像形成方法

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WO2011021052A2 (fr) 2009-08-21 2011-02-24 Sericol Limited Encre, appareil et procédé d'impression
EP2832553A1 (fr) * 2012-03-30 2015-02-04 FUJIFILM Corporation Procédé d'enregistrement par jet d'encre et matière imprimée
WO2016178989A1 (fr) * 2015-05-01 2016-11-10 Sun Chemical Corporation Composition d'encre ou de revêtement durcissable par de l'énergie et électriquement isolante
JP2017105902A (ja) * 2015-12-08 2017-06-15 コニカミノルタ株式会社 活性光線硬化型インクジェットインク及び画像形成方法

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4056658A1 (fr) * 2021-03-12 2022-09-14 Marabu GmbH & Co. KG Composition durcissable par exposition à un rayonnement
CN115044282A (zh) * 2022-08-17 2022-09-13 佛山市儒林化工有限公司 一种食品罐外用安全叠压无迁移uv光油及其制备方法
CN115044282B (zh) * 2022-08-17 2022-11-22 佛山市儒林化工有限公司 一种食品罐外用安全叠压无迁移uv光油及其制备方法

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