GB2510696A

GB2510696A - Printing on leather or synthetic leather using an aqueous primer layer and a hybrid ink

Info

Publication number: GB2510696A
Application number: GB201322228A
Authority: GB
Inventors: Nigel Gould; Andrew Philips
Original assignee: Sericol Ltd
Current assignee: Sericol Ltd
Priority date: 2012-12-14
Filing date: 2013-12-16
Publication date: 2014-08-13
Anticipated expiration: 2033-12-16
Also published as: GB2510696B; GB201222567D0; GB2512429A; GB2512429B; GB201322225D0; GB201322228D0

Abstract

A method of printing onto a leather or synthetic leather substrate comprises: depositing a primer layer onto the substrate, the primer comprising a thermoplastic resin and water; at least partially drying and/or curing the primer; inkjet printing a hybrid solvent/radiation curable ink onto the primer layer; drying and curing the hybrid ink layer; optionally depositing a protective layer onto the solvent-based ink layer, wherein the protective layer comprises a thermoplastic resin and a crosslinking agent; and drying and/or curing the protective layer; wherein the hybrid solvent/radiation-curable ink comprises at least 50% by weight organic solvent, based on the total weight of the ink, radiation-curable material and a photoinitiator and the primer and protective layer thermoplastic resins are selected from: polyurethane polymethacrylate, polyvinyl, poly(cellulose acetate butyrate), polyester, epoxy resin, hydrocarbon resin, ketone or aldehyde resin, amino resin, and copolymers and blends thereof; and wherein the protective coating further includes a solvent and/or monofunctional radiation-curable diluent, and, when a monofunctional radiation-curable diluents is present, a photoinitiator, The present invention also relates to a printed substrate obtainable by the method of the invention; the printed substrate is preferably an item of sportswear or sports equipment.

Description

Method of printing The present invention is concerned with a method of printing and more particularly to a method of printing onto a leather or synthetic leather substrate. The present invention is further concerned with a printed substrate obtainable by the method of the present invention.

The printing of ink images onto permeable leather or synthetic leather substrates for the production of sportswear and sports equipment, such as footballs and football boots, is a significant challenge.

Leather or synthetic leather presents an impervious (often thermoset) surface that is highly flexible and it is difficult to gain adhesion thereto. It is also essential that the finished printed substrate retains excellent flexibility, has high resistance to abrasion and is resistant to water.

The current process for printing ink onto a leather or synthetic leather substrate, for sportswear and sports equipment, is a screen printing process. Screen printing is currently used because such a process allows for the use of an ink having a wide viscosity range, allows for the alteration of film thickness and provides tough films. However, such a screen printing process is labour intensive. A large number of screens are required as individual screens are required for each colour and for each size of print. This is costly and time consuming.

Therefore an improved process for printing on such difficult substrates is required.

lnkjet printing is desirable and therefore an inkjet ink process has been contemplated in order to produce a printed image onto such difficult substrates because colours can be printed concurrently and any image size can be printed simply by varying the data file used.

However, the use of traditional UV curable inkjet inks in such an inkjet ink process is not a solution to the problem. Traditional UV curable inkjet inks which are inkjet printed onto such substrates provides good abrasion and reasonable adhesion. However, the high film weight which is deposited onto the substrate for such inks limits the formulation latitude available to achieve flexible films. To formulate films with the required high flexibility, the ink system must be largely based on UV curable monofunctional monomers. However, such films are soft and easily abraded. The inclusion of UV curable multifunctional monomers into the inkjet ink can provide the required resistance properties but the films produced are hard and brittle and do not meet the flexibility requirements. It is therefore not possible to provide the required combination of flexibility, resistance and adhesion.

The use of hybrid solvent/radiation-curable (e.g. UV) inks in such an inkjet ink process, in which a UV reactive binder is diluted in a volatile carrier, such as water or an organic solvent, is also not a solution to the problem. The inclusion of a volatile carrier results in the reduction of the film weight deposited, which lessens the adverse effect of the film on the substrate properties, thus allowing the use of higher functionality UV materials with the necessary resistance properties. In such inkjet systems, the image quality is fixed (or pinned) by applying heat to the substrate to evaporate partially the carrier solvent from the ink droplets to effect an increase in the ink viscosity, hence arresting the flow of the ink droplet and controlling the spread of the deposited ink droplet. However, the typical materials used for the production of the sportswear and sports equipment have relatively high film thickness and hence have a high heat capacity. The high heat capacity means that it is not possible to increase the temperature of the substrate quickly enough to effect the required viscosity increase in the ink droplets. The heat cannot penetrate through the substrate sufficiently, meaning that the pinning process is disabled, leading to excessive ink flow, yielding very poor image quality. In addition the non-permeable nature of the substrate severely limits any penetration of the solvent into the upper layers of the material further reducing the rate of viscosity rise and pinning efficiency. In other words, the time needed to pin the ink droplets is too long owing to the high heat capacity and impervious nature of the substrates, which results in the pooling of ink droplets and a poor quality image.

Hence there exists a requirement in the art for a method of printing onto a leather or synthetic leather substrate, which eliminates or reduces the aforementioned problems.

Accordingly, the present invention provides a method of printing onto a leather or synthetic leather substrate having a primer layer obtainable by providing the substrate, depositing a primer onto the substrate to form a primer layer, wherein the primer comprises a thermoplastic resin selected from polyurethane, polymethacrylate, polyvinyl, poly(cellulose acetate butyrate), polyester, epoxy resin, hydrocarbon resin, ketone or aldehyde resin, amino resin, and copolymers and blends thereof, and water, and at least partially drying the primer; the method comprising each of the following steps in order: (i) inkjet printing a hybrid solvent/radiation-curable ink onto the primer layer to form a hybrid solvent/radiation-curable ink layer, wherein the hybrid solvent/radiation-curable ink comprises at least 50% by weight organic solvent, based on the total weight of the ink, radiation-curable material and a photoinitiator; (ii)(a) optionally depositing a protective layer onto the hybrid solvent/radiation-curable ink layer, wherein the protective layer comprises: a thermoplastic resin selected from polyurethane, polymethacrylate, polyvinyl, poly(cellulose acetate butyrate), polyester, epoxy resin, hydrocarbon resin, ketone or aldehyde resin, amino resin, and copolymers and blends thereof, a solvent and/or radiation-curable diluent, and, when a monofunctional radiation-curable diluent is present, a photoinitiator, and a crosslinking agent; and (b) drying and curing the hybrid solvent/radiation-curable ink layer; wherein when (ii)(a) is present, (ii)(a) and (ii)(b) can be in either order, with the proviso that when step (ii)(b) occurs before step (iD(a), the method further comprises the step of drying and/or curing the protective layer.

The present invention further provides a method of printing onto a leather or synthetic leather substrate comprising each of the following steps in order: (i) providing the substrate; (ii) depositing a primer onto the substrate to form a primer layer, wherein the primer comprises: a thermoplastic resin selected from polyurethane, polymethacrylate, polyvinyl, poly(cellulose acetate butyrate), polyester, epoxy resin, hydrocarbon resin, ketone or aldehyde resin, amino resin, and copolymers and blends thereof, water; (Vi) at least partially drying the primer; (iv) inkjet printing a hybrid solvent/radiation-curable ink onto the primer layer to form a hybrid solvent/radiation-curable ink layer, wherein the hybrid solvent/radiation-curable ink comprises at least 50% by weight organic solvent, based on the total weight of the ink, radiation-curable material and a photoinitiator; (v)(a) optionally depositing a protective layer onto the hybrid solvent/radiation-curable ink layer, wherein the protective layer comprises: a thermoplastic resin selected from polyurethane, polymethacrylate, polyvinyl, poly(cellulose acetate butyrate), polyester, epoxy resin, hydrocarbon resin, ketone or aldehyde resin, amino resin, and copolymers and blends thereof, a solvent and/or radiation-curable diluent, and, when a monofunctional radiation-curable diluent is present, a photoinitiator, and a crosslinking agent; and (b) drying and curing the hybrid solvent/radiation-curable ink layer; wherein when (v)(a) is present, (v)(a) and (v)(b) can be in either order, with the proviso that when step (v)(b) occurs before step (v)(a), the method further comprises step of drying and/or curing the protective layer.

The present invention further provides a printed substrate and sportswear or sports equipment obtainable by the methods of the present invention.

The present invention will now be described with reference to the accompanying drawings, in which: Fig. 1 shows a schematic of the printed substrate obtainable by the method of the present invention; Fig. 2 shows a photograph of a printed substrate of the present invention; and Fig. 3 shows a photograph of a printed substrate in the absence of a primer layer of the present invention.

It has been found that depositing a primer as defined herein onto the substrate to form a primer layer aids the pinning of the hybrid solvent/radiation-curable ink. In the method of the invention the primer is deposited onto the substrate to form a primer layer. The primer layer is then at least partially dried.

The resultant at least partially dry primer layer is then deposited with the desired inkjet image by inkjet printing a hybrid solvent/radiation-curable ink onto the primer layer to form a hybrid solvent/radiation-curable ink layer. Without wishing to be bound by theory, it is believed that the primer layer absorbs some of the solvent from the inkjet droplets resulting in a rise in viscosity of the hybrid solvent/radiation-curable ink, thus pinning the ink droplets without the need for the application of heat.

The solvent is pulled into the primer and results in an increase in viscosity of the hybrid solvent/radiation-curable ink, preventing reticulation (or pooling) of the ink. This results in an ink image of excellent quality. The resulting film also has excellent flexibility and water, chemical and abrasion resistance. Thus, the method of the present invention allows for the production of a printed leather or synthetic leather substrate having an improved image quality, flexibility and abrasion, water and chemical resistance.

The substrate is a leather or synthetic leather substrate. Leather or synthetic leather substrates are non-porous, non-elongatable, but highly flexible which makes them difficult to print onto. The substrate is, however, typically found in the sportswear or sports equipment field. Sportswear and sports equipment require the printed substrate to have excellent flexibility, have high resistance to abrasion and be resistant to water.

Leather is a well-known material, created by the tanning of animal rawhide and skin. The tanning processes available to transform hides and skins into leather are well known and do not require further discussion. The leather may be natural leather, where the surface to be printed is obtained solely by tanning the rawhide and skin. Alternatively, the leather may be coated leather, where the leather is split (to provide two batches from one hide) and coated with polyurethane.

Synthetic leather is produced from a fibrous base layer, typically polyester, coated with polyurethane.

Again, synthetic leathers are well known in the art.

Thus, the substrate will be natural leather, polyurethane-coated leather, or synthetic leather (a material having a fibrous base layer coated with polyurethane). Thus, the surface which contacts the primer is either composed of leather or polyurethane.

The primer comprises a thermoplastic resin. The thermoplastic resin is selected from polyurethane, polymethacrylate, polyvinyl, poly(cellulose acetate butyrate), polyester, epoxy resin, hydrocarbon resin, ketone or aldehyde resin, amino resin, and copolymers and blends thereof Preferably, the resin is selected from polyurethane, polymethacrylate, polyvinyl, poly(cellulose acetate butyrate), polyester, and copolymers and blends thereof. More preferably, the resin is polyurethane and copolymers and blends thereof. Copolymers may be methacrylate copolymer which includes copolymers with different alkyl substituents like methyl, ethyl, propyl and butyl methacrylates, or polyvinyl copolymer which includes copolymers of vinyl chloride and vinyl acetate. Copolymers are typically chosen for their favourable glass transition temperatures. Blends are mixtures of polymers or copolymers, like methacrylate copolymer and polyvinyl copolymer blend or cellulose acetate butyrate and methacrylate copolymer blend.

The thermoplastic resin preferably has a weight-average molecular weight (Mw) of 1,500 to 200,000.

The Mw may be measured by known techniques in the art, such a gel permeation chromatography (GPC) using polystyrene standards. A suitable GPC apparatus for measuring Mw is an LC instrument having the following parameters -Column set: MiniMix E or MiniMix D (depending on molecular weight), Eluent: THF, Detector: UV/vis and/or ELS, Calibration: conventional vs polystryrene. This approach is applicable to polymers having a Mw of 400-400,000.

The resins are chosen such that the resultant primer layer which has been at least partially dried is resoluble in the solvent of the ink that will be deposited thereon and will soften with heat. It is important that the primer layer is not thermoset. If the primer layer were not resoluble in the solvent of the ink, the hybrid solvent/radiation-curable ink layer would fail to be pinned by the primer layer.

The resoluble nature of the thermoplastic resin can be tested in the primer layer by a solvent rub test.

The resultant primer layer must be soluble in the primary solvent of the ink after ito 50 double rubs and more preferably 1 to 20 double rubs. The primary solvent is the solvent present in the highest weight percent. Where two or more solvents are present in the same amount (this rarely occurs), the primary solvent is taken as a mixture of those solvents. The double rub test is well known in the art.

The primer is applied to the substrate by any suitable means. It is then at least partially dried. One then takes a lint-free (cotton) cloth saturated in the solvent. One then carries out a double rub, each rub being 10 cm. The number of rubs is counted until the substrate is visible under the primer.

Optionally a coloured solvent-based ink, preferably having one rub solvent resistance, may be printed under the primer so that the colour is easily visible. The substrate will then become visible when the colour is removed.

When it is stated that the primer is "at least partially" dried, it means that the drying is performed to a sufficient extent that the primer layer retains its resolubility properties as determined by the above-described double solvent rub test.

The thermoplastic resin may be a passive/inert thermoplastic resin or a radiation-crosslinkable (e.g. UV) thermoplastic resin. A UV crosslinkable thermoplastic resin is preferably acrylate functionalised and is hence crosslinkable when exposed to UV radiation.

Preferably, the primer comprises polyurethane. Preferably, the primer comprises a passive polyurethane resin or UV crosslinkable polyurethane. The UV crosslinkable polyurethane is preferably an aqueous polyurethane dispersion (PUD) which is acrylate functionalised. The aqueous PUD comprises acrylate functionalised polyurethane that is dispersed in water and is hence crosslinkable when exposed to UV radiation.

The primer comprises water and is preferably in the form of an aqueous polymer dispersion.

A particularly preferred primer is a water-based polyurethane dispersion.

Preferably, the ink is substantially free of organic solvent and radiation-curable diluent (typically monofunctional), although some organic solvent and monofunctional radiation-curable diluent will typically be present as impurities in the components of the inks, and such levels are tolerated. For example, the ink may comprise less than 5% by weight of organic solvent and radiation-curable diluent combined, more preferably less than 2% by weight of organic solvent and radiation-curable diluent combined and most preferably less than 1% by weight of organic solvent and radiation-curable diluent combined, based on the total weight of the ink. In a preferred embodiment, water is the sole liquid phase in the primer.

The primer optionally comprises a flow aid. Preferable flow aids include silicone fluids, fluoro surfactants, silicone defoamers, non-silicone defoamers and levelling agents. Fluorosurfactants are particularly preferred.

The primer layer can optionally contain inorganic materials such as extender powders and the like waxes, matting agents and in the case of UV curable systems, photoinitiators.

The primer layer may optionally further comprise a humectant/waterbased retarder. Preferred examples include mono propylene glycol, mono ethylene glycol and mixtures thereof The primer layer may also optionally comprise precipitated calcium carbonate to reduce the finish.

In a preferred embodiment the primer layer further comprises a crosslinking agent, such as a propylene-imine crosslinkerto increase the chemical resistance properties of the primer layer.

The primer layer may optionally contain a thickener, such as an anionic polyacrylate copolymer.

The primer is deposited onto the substrate to form a primer layer. The primer layer may be deposited onto the substrate by any means known in the art. Preferably, the primer layer is deposited onto the substrate by screen printing, flexographic printing, inkjet printing, bar coating spraying, curtain coating, slit coating or wipe on by hand. Preferably, the primer is deposited onto the substrate by screen printing flatbed or rotary, flexographic printing, bar coating, spraying, curtain coating or slit coating.

The primer is then at least partially dried to form a primer layer.

It should be noted that the terms "dry" 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. Herein, however, by "drying" is meant the removal of the solvent by evaporation and by "curing" is meant the polymerisation and/or crosslinking of the radiation-curable material.

The primer layer is at least partially thermally dried and is preferably fully dried to evaporate the water before the hybrid solvent/radiation-curable ink is deposited on the surface of the primer layer.

A key factor for the pinning efficiency of the primer layer is the resolubility of the primer layer in the solvent used in the hybrid solvent1radiation-curable ink which is to be deposited onto the primer layer.

In a preferred embodiment, the at least partially dried, preferably fully dried, films are readily resoluble by the solvent of the ink. The at least partially dried, preferably fully dried, films will still be receptive to solvent from the overlaying ink because it leaves behind a thermoplastic resin that is resoluble.

The thermally dried water-based UV crosslinkable thermoplastic resin dispersion primer must not be UV crosslinked before the ink is deposited as this would render the primer layer insoluble and non-receptive in the solvent and hence it could not perform its pinning role.

The primer layer preferably has a thickness of 40 microns or less, more preferably 20 microns or less and most preferably 10 microns or less, based on the dry film thickness. The dry film thickness means the thickness of the film after it is at least partially dried and/or at least partially cured, i.e. when the primer layer receives the ink. It is surprising that such a small amount of primer provides the required image quality combined with the necessary robustness and flexibility. The thickness is preferably 1 micron or above, more preferably 5 microns or above. Film thicknesses can be measured using a confocal laser scanning microscope.

The inkjet ink is a hybrid solvent/radiation-curable ink jet ink which comprises at least 50% by weight organic solvent, based on the total weight of the ink, radiation-curable material and a photoinitiator.

The ink comprises a modified ink binder system. The presence of a radiation-curable material and a photoinitiator in the ink means that crosslinked polymers can be formed in the dried ink film, leading to improved adhesion to a range of substrates and improved resistance to solvents. The presence of organic solvent means that the advantageous properties of solvent-based inkjet inks are maintained.

By "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 radiation-curable material may optionally comprise a radiation-curable oligomer. The oligomers may possess different degrees of functionality, and a mixture including combinations of mono, di, tn and higher functionality monomersloligomers may be used.

Radiation-curable oligomers suitable for use in the present invention comprise a backbone, for example a polyester, urethane, epoxy or polyether backbone, and one or more radiation polymerisable groups. The oligomer preferably comprises a urethane backbone. The polymerisable group can be any group that is capable of polymerising upon exposure to radiation. Preferably the oligomers are (meth)acrylate oligomers. Preferably they are multifunctional and most preferably have a functionality of 2-6.

Particularly preferred radiation-curable materials are urethane acrylate oligomers as these have excellent adhesion and elongation properties. Most preferred are tn-, tetra-, penta-, hexa-or higher functional urethane acrylates, particularly hexafunctional urethane acrylates as these yield films with good solvent resistance.

Other suitable examples of 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.

Preferred oligomers have a molecular weight of 450 to 4,000, more preferably 600 to 4,000.

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.

In one embodiment the radiation-curable oligomer polymerises by free-radical polymerisation. The radiation-curable oligomer cures upon exposure to radiation in the presence of a photoinitiatorto form a crosslinked, solid film. The resulting film has good adhesion to substrates and good solvent resistance. Any radiation-curable oligomer that is compatible with the other ink components and that is capable of curing to form a crosslinked, solid film is suitable for use in the ink. Thus, the ink formulator is able to select from a wide range of suitable oligomers.

Preferred oligomers for use in the invention have a viscosity of 0.5 to 20 Pa.s at 60°C, more preferably 5 to 15 Pa.s at 60°C and most preferably 5 to 10 Pa.s at 60°C. Oligomer viscosities can be measured using an ARG2 rheometer manufactured by TA. Instruments, which uses a 40 mm oblique /2° steel cone at 60°C with a shear rate of 25 seconds1.

The ink optionally contains radiation-curable monomers as the radiation-curable material. Suitable free-radical polymerisable monomers are well known in the art and include (meth)acrylates, a,-unsaturated ethers, vinyl amides and mixtures thereof.

The monomers may possess different degrees of functionality, and a mixture including combinations of mono, di, tn and higher functionality monomers/oligomers may be used.

Monofunctional (meth)acrylate monomers are well known in the art and are preferably the esters of acrylic acid. Preferred examples include phenoxyethyl acrylate (PEA), cyclic TMP formal acrylate (CTFA), isobornyl acrylate (IBOA), tetrahydrofurfuryl acrylate (THFA), 2-(2-ethoxyethoxy)ethyl acrylate, octadecyl acrylate (ODA), tridecyl acrylate (TDA), isodecyl acrylate (IDA) and lauryl acrylate.

Suitable multifunctional (meth)acrylate monomers include di-, tn-and tetra-functional monomers.

Examples of the multifunctional acrylate monomers that may be included in the ink-jet inks include hexanediol diacrylate, trimethylolpropane triacrylate, pentaerythritol triacrylate, polyethylene glycol diacrylate (for example tetraethylene glycol diacrylate), dipropylene glycol diacrylate, tri(propylene glycol) triacrylate, neopentyl glycol diacrylate, bis(pentaerythritol) hexaacrylate, and the acrylate esters of ethoxylated or propoxylated glycols and polyols, for example, propoxylated neopentyl glycol diacrylate, ethoxylated trimethylolpropane triacrylate, and mixtures thereof.

Suitable multifunctional (meth)acrylate monomers also include esters of methacrylic acid (i.e. methacrylates), such as hexanediol dimethacrylate, trimethylolpropane trimethacrylate, triethyleneglycol dimethacrylate, diethyleneglycol dimethacrylate, ethyleneglycol dimethacrylate, 1,4-butanediol dimethacrylate. Mixtures of (meth)acrylates may also be used.

(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.

In an alternative embodiment of the invention, the radiation-curable material is capable of polymerising by cationic polymerisation. Suitable materials include, oxetanes and epoxides (e.g. cycloaliphatic epoxides, bisphenol A epoxides and epoxy novolacs). The radiation-curable material according to this embodiment may comprise a mixture of cationically curable monomer and oligomer.

For example, the radiation-curable material may comprise a mixture of an epoxide oligomer and an oxetane monomer.

The radiation-curable material can also comprise a combination of free-radical polymerisable and cationically polymerisable materials.

o,13-Unsaturated ether monomers can polymerise by free-radical polymerisation and may be useful for reducing the viscosity of the ink when used in combination with one or more (meth)acrylate monomers. Examples are well known in the art and include vinyl ethers such as triethylene glycol divinyl ether, diethylene glycol divinyl ether, 1,4-cyclohexanedimethanol divinyl ether and ethylene glycol monovinyl ether. Mixtures of ci,13-unsaturated ether monomers may be used.

N-Vinyl amides and N-(meth)acryloyl amines may also be used in the ink. 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 the (meth)acrylate monomers. Preferred examples are N-vinyl caprolactam (NVC) and N-vinyl pyrrolidone (NVP). Similarly, 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 the (meth)acrylate monomers. A preferred example is N-acryloylmorpholine (ACMO).

Preferably the ink comprises 10 to 30% by weight of radiation-curable material based on the total weight of the ink, preferably at least 12% by weight, more preferably 10 to 20% by weight, based on the total weight of the ink.

The ink includes one or more photoinitiators. The ink includes a free-radical polymerisable material and hence the photoinitiator system includes a free-radical photoinitiator.

The free-radical photoinitiator can be selected from any of those known in the art. For example, benzophenone, 1 -hydroxycyclohexyl phenyl ketone, 1 -[4-(2-hydroxyethoxy)-phenyl]-2-hydroxy-2-methyl-i -propane-i -one, 2-benzyl-2-dimethylamino-(4-morpholinophenyl)butan-1 -one, isopropyl thioxanthone, benzil dimethylketal, bis(2,6-dimethylbenzoyl)-2,4,4-trimethylpentylphosphine oxide or mixtures thereof Such photoinitiators are known and commercially available such as, for example, under the trade names Irgacure and Darocur (from Ciba) and Lucerin (from BASF).

In the case of a cationically curable system, any suitable cationic initiator can be used, for example sulfonium or iodonium based systems. Non limiting examples include: Rhodorsil Fl 2074 from Rhodia; MC AA, MC BB, MC CC, MC CC PF, MC SD from Siber Hegner; UV938Oc from Alfa Chemicals; Uvacure 1590 from UCB Chemicals; and Esacure 1064 from Lamberti spa.

Preferably the photoinitiator is present in an amount of ito 20% by weight, preferably 4 to 10% by weight, based on the total weight of the ink.

The ink contains an organic solvent. The organic solvent is in the form of a liquid at ambient temperatures and is capable of acting as a carrier for the remaining components of the ink. The organic solvent component of the ink may be a single solvent or a mixture of two or more solvents.

As with known solvent-based inkjet inks, the organic solvent used in the ink is required to evaporate from the printed ink, typically on heating, in order to allow the ink to dry. The solvent can be selected from any solvent commonly used in the printing industry, such as glycol ethers, glycol ether esters, alcohols, ketones, esters, organic carbonates, lactones and pyrrolidones.

The organic solvent is present in an amount of at least 50% by weight, preferably at least 60% by weight, based on the total weight of the ink.

Known solvent-based inkjet inks dry solely by solvent evaporation with no crosslinking or polymerisation occurring. The film produced therefore has limited chemical resistance properties. In order to improve resistance of prints to common solvents such as alcohols and petrol, binder materials that have limited solubility in these solvents are added to the ink. The binder is typically in solid form at 25°C so that a solid printed film is produced when solvent is evaporated from the ink.

Suitable binders such as vinyl chloride copolymer resins generally have poor solubility in all but the strongest of solvents such as glycol ether acetates and cyclohexanone, both of which are classified as "harmful" and have strong odours. In order to solubilise the binder, these solvents are generally addedtotheink.

The ink includes radiation-curable material that cures as the ink dries and it is not therefore necessary to include a binder in the ink in order to provide a printed film having improved solvent resistance. In one embodiment of the invention the organic solvent is not therefore required to solubilise a binder such as a vinyl chloride copolymer resin, which means that the ink formulator has more freedom when selecting a suitable solvent or solvent mixture.

In a preferred embodiment the organic solvent is a low toxicity and/or a low odour solvent. Solvents that have been given VOC exempt status by the United States Environmental Protection Agency or European Council are also preferred.

The most preferred solvents are selected from glycol ethers and organic carbonates and mixtures thereof. Cyclic carbonates such as propylene carbonate and mixtures of propylene carbonate and one or more glycol ethers are particularly preferred.

Alternative preferred solvents include lactones, which have been found to improve adhesion of the ink to PVC substrates. Mixtures of lactones and one or more glycol ethers, and mixtures of lactones, one or more glycol ethers and one or more organic carbonates are particularly preferred. Mixtures of gamma butyrolactone and one or more glycol ethers, and mixtures of gamma butyrolactone, one or more glycol ethers and propylene carbonate are particularly preferred.

In another embodiment of the invention, dibasic esters and/or bio-solvents may be used.

Dibasic esters are known solvents in the art. They can be described as di(C1-C4 alkyl) esters of a saturated aliphatic dicarboxylic acid having 3 to 8 carbon atoms having following general formula: R1 O)LA)LOR2 in which A represents (CH2)15, and R1 and R2 may be the same or different and represent C1-C4 alkyl which may be a linear or branched alkyl radical having 1 to 4 carbon atoms, preferably methyl or ethyl, and most preferably methyl. Mixtures of dibasic esters can be used.

Bio-solvents, or solvent replacements from biological sources, have the potential to reduce dramatically the amount of environmentally-polluting VOCs released in to the atmosphere and have the further advantage that they are sustainable. Moreover, new methods of production of bio-solvents derived from biological feedstocks are being discovered, which allow bio-solvent production at lower cost and higher purity.

Examples of bio-solvents include soy methyl ester, lactate esters, polyhydroxyalkanoates, terpenes and non-linear alcohols, and D-limonene. Soy methyl ester is prepared from soy. The fatty acid ester is produced by esterification of soy oil with methanol. Lactate esters preferably use fermentation-derived lactic acid which is reacted with methanol and/or ethanol to produce the ester. An example is ethyl lactate which is derived from corn (a renewable source) and is approved by the FDA for use as a food additive. Polyhydroxyalkanoates are linear polyesters which are derived from fermentation of sugars or lipids. Terpenes and non-linear alcohols may be derived from corn cobs/rice hulls. An example is D-limonene which may be extracted from citrus rinds.

Other solvents may be included in the organic solvent component. A particularly common source of other solvents is derived from the way in which the colouring agent is introduced into the inkjet ink formulation. The colouring agent is usually prepared in the form of a pigment dispersion in a solvent, e.g. 2-ethylhexyl acetate. The solvent tends to be around 40 to 50% by weight of the pigment dispersion based on the total weight of the pigment dispersion and the pigment dispersion typically makes up around 5 to 15% by weight of the ink and sometimes more.

The ink is preferably substantially free of water, although some waterwill typically be absorbed by the ink from the air or be present as impurities in the components of the inks, and such levels are tolerated. For example, the ink may comprise less than 5% by weight of water, more preferably less than 2% by weight of water and most preferably less than 1% by weight of water, based on the total weight of the ink.

The ink may also contain a passive (or "inert") thermoplastic 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, resin is not a radiation-curable material.

The resin may be selected from epoxy, polyester, vinyl, ketone, nitrocellulose, phenoxy or acrylate resins, or a mixture thereof and is preferably a poly(methyl (meth)acrylate) resin. The resin has a weight-average molecular weight of 1,500-200,000, as determined by GPO with polystyrene standards as previously described hereinabove.

The ink may be a coloured or a colourless ink. By "colourless" is meant that the ink is free of colorant such that no colour can be detected by the naked eye. Minor amounts of colorant that do not produce colour that can be detected by the eye can be tolerated, however. Typically the amount of colorant present will be less than 0.3% by weight based on the total weight of the ink, preferably less than 0.1%, more preferably less than 0.03%. Colourless inks may also be described as "clear" or "water white". Colourless inks may also be used as a varnish, where it is applied over a coloured ink. For the avoidance of doubt, coloured inks include white inks.

The coloured inks comprise at least one colouring agent. The colouring agent may be either dissolved or dispersed in the liquid medium of the ink. Preferably 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 plc), 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. Especially useful are black and the colours required for trichromatic process printing. Mixtures of pigments may be used.

In one aspect the following pigments are preferred. 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 20 weight% or less, preferably 10 weight% or less, more preferably 8 weight% or less and most preferably 2 to 5% by weight, 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 weight%, or25 weight% based on the total weight of the ink.

The inkjet ink exhibits a desirable low viscosity (200 mPa.s or less, preferably 100 mPa.s or less, more preferably 25 mPa.s or less and most preferably 10 mPa.s or less, at 25°C).

Other components of types known in the art may be present in the ink to improve the properties or performance. These components may be, for example, surfactants, defoamers, dispersants, synergists for the photoinitiator, stabilisers against deterioration by heat or light, reodorants, flow or slip aids, biocides and identifying tracers.

The inkjet ink preferably comprises a radiation-curable material, a photoinitiator, a colorant and a solvent.

The ink may be prepared by known methods such as stirring with a high-speed water-cooled stirrer, or milling on a horizontal bead-mill.

The hybrid solvent/radiation-curable ink is deposited onto the at least partially dried primer layer to form a hybrid solvent/radiation-curable ink layer or deposited inkjet image by inkjet printing. lnkjet printing is well known in the art. The image may be deposited using a roll-to-roll solvent UV hybrid printer. Alternatively, the inks may be deposited using a flatbed printer where the print head scans across a stationary substrate before it is advanced ready for the next print swathe to deposited. In this case there is an optional top down heater or air knife to assist the efficiency of the pinning process by removal of the solvent carrier form the solvent UV hybrid ink. Following the pinning process, in one embodiment the print is removed manually from the printer to a separate thermal drier where the remainder of the solvent carrier is removed from the ink before finally curing the image by exposure to a source of actinic radiation. This final curing stage can either be completed in-line by using a combination drier fitted with both a source of heat and a UV curing system or using separate thermal drying and UV curing systems.

In a further embodiment the printing pinning, thermal drying and final UV curing can be completed in-line. After deposition of the image with the solvent UV hybrid ink and pinning on the primed material, the print is transferred to a thermal drying apparatus before finally passing under a source of actinic radiation to effect the final cure process. The transfer of the print through the combination printer can either be accomplished using sheets of the substrate held in grippers that move it through each stage of the process or alternatively via a roll-to-roll process where the primed substrate is moved as a web through each stage by the use of rollers. In a further embodiment the roll-to-roll web production process above can be modified to apply the primer layer in-line using a suitable method, for example rotary screen printing, flexographic printing, roller coating, bar coating or slit coating The hybrid solvent/radiation-curable ink layer may then be dried and cured.

The printing is preferably all performed by inkjet printing, e.g. on a roll-to-roll printer or fiat-bed printer.

Evaporation of the solvent can occur simply by exposure of the inks to the atmosphere, but the inks may also be heated to accelerate evaporation. In addition, the inks are exposed to actinic radiation to cure the ink.

The ink can be printed using inkjet printers that are suitable for use with solvent-based inkjet inks, in combination with a source of actinic radiation. The features of printers that are suitable for printing solvent-based inkjet inks are well known to the person skilled in the art and include the features described below.

The printing apparatus may comprise a means for evaporating solvent from the ink at the appropriate time after the ink has been applied to the substrate. Any means that is suitable for evaporating solvent from known solvent-based inkjet inks can be used in the apparatus. Examples are well known to the person skilled in the art and include dryers, heaters, air knives and combinations thereof.

In one embodiment, the solvent is removed by heating. Heat may be applied through the substrate and/or from above the substrate, for example by the use of heated plates (resistive heaters, inductive heaters) provided under the substrate or radiant heaters (heater bars, IR lamps, solid state IR) provided above the substrate. In a preferred embodiment, the ink can be jetted onto a preheated substrate that then moves over a heated platen. The apparatus may comprise one or more heaters.

As previously stated however, typical materials used for the production of the sportswear and sports equipment have relatively high film thickness and hence have a high heat capacity. The high heat capacity means that it is not possible to increase the temperature of the substrate quickly enough to effect the required viscosity increase in the ink droplets. The heat cannot penetrate through the substrate sufficiently, meaning that the pinning process is disabled, leading to excessive ink flow, yielding very poor image quality. In other words, the time needed to pin the ink droplets is too long owing to the high heat capacity of the substrates, which results in the pooling of ink droplets and a poor quality image.

Accordingly, the primer layer absorbs some of the solvent from the inkjet droplets resulting in a rise in viscosity of the hybrid solvent/radiation-curable ink, thus pinning the ink droplets without the need for the application of heat. The solvent is pulled into the primer and results in an increase in viscosity of the hybrid solvent/radiation-curable ink, preventing reticulation (or pooling) of the ink.

When printing the ink, a significant portion of the solvent is preferably allowed to evaporate before the ink is cured. Preferably substantially all of the solvent is evaporated before the ink is finally cured.

This is achieved by subjecting the printed ink to conditions that would typically dry conventional solvent-based inkjet inks. In the case of the ink, such conditions will remove most of the solvent but it is expected that trace amounts of solvent will remain in the film given the presence of the radiation-curable component in the ink.

Unlike standard solvent-based inks, once the solvent has evaporated, the ink is not expected to be completely solid. Rather, what remains on the surface is a high viscosity version of a radiation-curable ink. The viscosity is sufficiently high to inhibit or significantly hinder ink flow and prevent image degradation in the timescale that is needed to post-cure the ink. Upon exposure to a radiation source, 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 ito 20 pm, preferably ito 10 pm, for example 2 to 5 pm. Film thicknesses can be measured using a confocal laser scanning microscope.

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 (LED5), 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.

Preferably the source of actinic radiation is a source that does not generate ozone when in use.

The source of UV radiation could be situated off-line in a dedicated conveyor UV curing unit, such as the SUVD Svecia UV Dryer. Preferably, however, the source of radiation is situated in-line, which means that the substrate does not have to be removed from the printing apparatus between the heating and curing steps.

The radiation source can be mobile, which means that the source is capable of moving back and forth across the print width, parallel with the movement of the printhead.

In one embodiment, one or more sources of actinic radiation are placed on a carriage that allows the source of actinic radiation to traverse the print width. The carriage may be placed up and downstream of the printer carriage in allow irradiation before and after evaporation of the solvent. In this embodiment the source of actinic radiation moves independently of the printer carriage and movement of the printhead does not therefore have to be slowed in order to provide adequate time for solvent evaporation. Thus, overall productivity can be improved.

When the source of radiation is provided on separate carriage, it is necessary to provide an additional carriage rail, motor and control systems. This adaptation can lead to large increases in equipment costs.

Preferably the source of radiation is static. This means that the source does not move backwards and forwards across the print width of the substrate when in use. Instead the source of actinic radiation is fixed and the substrate moves relative to the source in the print direction.

When the source of actinic radiation is provided in the print zone of the printer, light contamination at the printhead, which could lead to premature curing in the nozzle, must be avoided. Adaptations to prevent light contamination, such as lamp shutters, give rise to additional costs. The source of radiation is therefore preferably located outside the print zone of the printing apparatus. By print zone is meant the region of the printing apparatus in which the printhead can move and therefore the region in which ink is applied to the substrate.

Static curing units preferably span the full print width, which is typically at least 1.6 m for the smaller wide format graphics printers. Fluorescent tubes, mercury discharge lamps, and light emitting diodes can be used as static curing units.

Any of the sources of actinic radiation discussed herein may be used for the irradiation of the inkjet ink. A suitable dose would be greater than 200 mJ/cm2, more preferably at least 300 mJ/cm2 and most preferably at least 500 mJ/cm2. 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 J/cm.

The wavelength of the pinning source is typically 200-700 nm, preferably 300-500 nm and most preferably 350-450 nm.

The delay between evaporating the solvent and providing a final cure of the ink is typically at least 1 minute after jetting.

High and medium pressure mercury discharge lamps may be used.

In another embodiment of the invention the source of radiation comprises one or more flash lamps.

Flash lamps operate by discharge breakdown of an inert gas, such as xenon or krypton, between two tungsten electrodes. Unlike mercury discharge lamps, flash lamps do not need to operate at high temperature. Flash lamps also have the advantage of switching on instantaneously, with no thermal stabilisation time. The envelope material can also be doped, to prevent the transmission of wavelengths that would generate harmful ozone. Flash lamps are therefore economical to operate and therefore suitable for use.

When the primer contains a crosslinkable resin, this material remains uncured after the at least partial drying step. In this case, after deposition and thermal drying of the hybrid solvent/radiation-curable ink jet ink, both the primer layer and the hybrid solvent/radiation-curable ink layer are cured concurrently.

A protective layer may optionally be deposited onto the hybrid solvent/radiation-curable ink layer. The protective layer may be deposited before or after the step of drying and curing the hybrid solvent/radiation-curable ink layer.

The protective layer comprises a resin selected from polyurethane, polymethacrylate, polyvinyl, poly(cellulose acetate butyrate), polyester, epoxy resin, hydrocarbon resin, ketone or aldehyde resin, amino resin, and copolymers and blends thereof. Preferably, the protective layer comprises polyurethane.

The protective layer further comprises a solvent and/or radiation-curable diluent. The solvent is the same as those discussed hereinabove with reference to the ink, with the proviso that the solvent should not be selected such that they will react with the crosslinker. For example, in the case where an isocyanate crosslinker is used, hydroxyl solvents that will react with this should be avoided, e.g. water, alcohols and glycol mono ethers. The radiation-curable diluent is not so limited, although when a radiation-curable diluent is present, a photoinitiator is required. The monofunctional monomers described with reference to the primer layer may be used. Alternatively, or in addition, other radiation-curable materials may be used, including multifunctional monomers.

Examples of the multifunctional acrylate monomers that may be included in this layer include hexanediol diacrylate, trimethylolpropane triacrylate, pentaerythritol triacrylate, polyethylene glycol diacrylate (for example tetraethylene glycol diacrylate), dipropylene glycol diacrylate, tri(propylene glycol) triacrylate, neopentyl glycol diacrylate, bis(pentaerythritol) hexaacrylate, and the acrylate esters of ethoxylated or propoxylated glycols and polyols, for example, propoxylated neopentyl glycol diacrylate, ethoxylated trimethylolpropane triacrylate, and mixtures thereof Suitable multifunctional (meth)acrylate monomers also include esters of methacrylic acid (i.e. methacrylates), such as hexanediol dimethacrylate, trimethylolpropane trimethacrylate, triethyleneglycol dimethacrylate, diethyleneglycol dimethacrylate, ethyleneglycol dimethacrylate, 1,4-butanediol dimethacrylate. Mixtures of (meth)acrylates may also be used.

Suitable photoinitiators are the same as those described with reference to the ink.

The protective layer further comprises a crosslinking agent. The crosslinking agent should be capable of reacting with the resin system used in the protective top coat. Depending on the resin selected suitable crosslinkers include amines, acids, aziridines, carbodimides and isocyanates. Preferably, the crosslinking agent is isocyanate as these have the widest range of reactivity.

The protective layer may comprise formulations used for the primer, together with a crosslinking agent. The crosslinker may optionally also crosslink with the primer to provide additional toughness to the film.

The protective layer is applied by any means known in the art but is preferably applied by traditional printing process such screen printing, fiexographic printing or roller coating.

In the event that the step of drying and curing the hybrid solvent/radiation-curable ink layer occurred before the deposition of the protective layer, the protective layer is then thermally dried and/or cured.

In the event that the step of drying and curing the hybrid solvent/radiation-curable ink layer did not occur before the deposition of the protective layer, the protective layer is then thermally dried and radiation cured. The hybrid solvent/radiation-curable ink layer is cured through the protective layer.

When the primer contains a crosslinkable resin, this remains uncured after the at least partial drying step. In this case, after deposition and thermal drying of the hybrid solvent/radiation-curable ink jet ink, and optional deposition of the protective layer, both the primer layer and the hybrid solvent/radiation-curable ink layer are cured concurrently through the protective layer.

The present invention also provides a printed substrate obtainable by the method of the present invention. Preferably, the substrate is sportswear or sports equipment.

The invention will now be described with reference to the following examples, which are not intended to be limiting.

Examples

Example 1

A primer, as detailed in Table 1, was prepared by mixing the components in the given amounts.

Amounts are given as weight percentages based on the total weight of the primer.

Table 1

Primer Amount Anionic dispersion of aliphatic polyester-94.67 polyurethane (U2101) Capstone FS-31 0.20 Rheovis®HS 1152 0.13 Dow corning Additive 65 2.50 Mono propylene glycol 2.50 U2101 from Alberdingk Boley is an anionic dispersion of an aliphatic polyester-polyurethane without solvents and free from residual isocyanate groups. U2101 has a solids content of 59.5-61.5% with the remainder being water, which means that water is present in the primer in an amount of approximately 38% by weight, based on the total weight of the primer. U21 01 has a pH value of 7.5- 9.5 and an elongation at break (%) of 800, The elongation at break is tested by drawing down a film of the material on to a highly elogatable polymer support (greater than 800%) using a K2 bar depositing a wet film weight of 12 microns. The film is then dried at 60°C for 3 minutes. The print is then allowed to equilibrate for 24 hours before being tested on an Instron tension tester for film break point during elongation.

Capstone FS-31 from Du Pont is a partially fluorinated alcohol substituted glycol surfactant which is used as a flow additive.

Rheovis® HS1 152 from BASF is an anionic polyacrylate copolymer. It acts as a thickener and is based on acrylic polymer technology with side groups designed to provide an associate thickening mechanism. Rheovis® HS1152 has a pH value of 3-3.5.

Additive 65 from Dow Corning is a silicone based defoamer for water-based systems and is 50% active.

Mono propylene glycol is a humectant'water retarder, which is used to improve open time during the application process by reducing evaporation of water from the primer during application and improves the screen stability of the primer.

The primer was applied to the substrate by drawing down a film onto the substrate using a No. 2 K bar coater. The substrate used was 220 micron gloss white genotherm (PVC). The film was dried at 60°C for 3 minutes.

The anionic dispersion of an aliphatic polyester-polyurethane has a high molecular weight but as the polymer is in the form of a dispersed phase in water, the viscosity is very low. The high molecular weight has significant advantages. After evaporation of water this material forms a relatively tough dry film but which is still solvent sensitive.

Hybrid solvent/radiation-curable ink formulations shown in Table 2 were prepared by mixing the components in the given amounts. Amounts are given as weight percentages based on the total weight of the ink.

Table 2

Cyan ink Magenta ink Yellow ink Black ink Component _________________________ (ink 1) (ink 2) (ink 3) (ink 4) Gamma butyrolactone 16.3 15.5 15.6 16.5 Diethylene glycol diethyl ether 53.1 51.7 52.4 51.4 Nippon Goshei UV7630B 16 15 12 19.5 Cyan pigment dispersion 6 --- Magenta pigment dispersion -11.2 -- Yellow pigment dispersion --13.4 -Black pigment dispersion ---6 Irgacure 819 4 4 4 4 Irgacure 2959 2 2 2 2 UV 12 stabiliser 0.5 0.5 0.5 0.5 Byk331 0.1 0.1 0.1 0.1 The substrate was then fixed to the substrate roll of a Mimaki JV400 SUV printer loaded with hybrid solvent/radiation-curable inks as detailed in Table 2. After the initial printing process, the print was dried for 3 minutes at 60°C and then passed through a UV drier fitted with lxi 00 w/cm medium pressure mercury lamp at 25 rn/minute to effect cure of the hybrid solvent/radiation-curable ink.

The substrate was positioned such that part of the image was deposited on the primed area and part on non-primed areas of the substrate.

The higher functionality (meth)acrylate oligomer used in the hybrid ink gives a far higher resistance film than that of a standard UV inkjet ink.

The non-primed and primed areas of the hybrid UV solvent print on the substrate were evaluated.

Specifically, the drop spread and bleed were compared between primed and non-primed areas of the print using Discovery USB microscope VMS-004 supplied by Veho. In all cases the image quality was far higher in the primed area of the substrate. Where the primer was on the surface, the pinning was excellent. The image quality was excellent; it was glossy and had excellent colour density. The print shows that the ink droplets are still well defined. In contrast, in non-primed areas, the print was very grainy owing to excessive ink spreading, reticulation and blending of the ink droplets. Without wishing to be bound by theory, it is believed that the primer absorbs the solvent in the hybrid solvent/radiation-curable ink causing a rapid rise in viscosity of the ink and thus arresting the spread of the droplet. In non-primed areas, excessive ink pooling was seen leading to a grainy image with poor resolution.

The choice of the thermoplastic resin is partly determined by the substrate to be used; the primer must have good adhesion to the material being used. In addition, the at least partially dried primer layer must have good resolubility in the carrier solvent used in the hybrid solvent/radiation-curable ink.

Example 2

A primer, as detailed in Table 3, was prepared by mixing the components in the given amounts.

Table 3

Primer Amount Anionic dispersion of aliphatic polyester-90.54 polyurethane (U2101) Capstone FS-31 0.20 Rheovis® F-IS 1152 0.26 Dow corning Additive 65 2.50 Precipitated calcium carbonate 4.00 Mono propylene glycol 2.50 U21 01, Capstone FS-31, Rheovis® HS1 152, Additive 65 and mono propylene glycol are as discussed hereinabove for Example 1. Calcium carbonate supplied by Minerals Technologies is added to reduce the finish.

The substrate was then fixed to the substrate roll of a Mimaki JV400 SUV printer loaded with hybrid solvent/radiation-curable inks as detailed in Table 2. After the initial printing process, the print was dried for 3 minutes at 60°C and then passed through a UV drier fitted with lxi 00 w/cm medium pressure mercury lamp at 25 m/minute to effect cure of the hybrid solvent/radiation-curable ink.

Specifically, the drop spread and bleed were compared between primed and non-primed areas of the print using Discovery USB microscope VMS-004 supplied by Veho. Once again, in all cases the image quality was far higher in the primed area of the substrate. Where the primer was on the surface, the pinning was excellent. The image quality was excellent; it was glossy and had excellent colour density. The print shows that the ink droplets are still well defined. In contrast, in non-primed areas, the print was very grainy owing to excessive ink spreading, reticulation and blending of the ink droplets. Without wishing to be bound by theory, it is believed that the primer absorbs the solvent in the hybrid solvent/radiation-curable ink causing a rapid rise in viscosity of the ink and thus arresting the spread of the droplet. In non-primed areas, excessive ink pooling was seen leading to a grainy image with poor resolution.

Example 3

A protective layer, as detailed in Table 4, can optionally be applied to the hybrid solvent1radiation-curable ink layers of Example 1. The protective layer was prepared by mixing the components of Table 4 in the given amounts. Amounts are provided as weight percentages based on the total weight of the ink.

Table4

Protective layer Amount Primer of TableS 95.0 Desmodur N75 (isocyanate functional crosslinker) 5.0

Table 5

Primer Amount (weight percentage based on total weight of primer) Polyurethane (Estane 5715 P) 31.78 Solvent naptha 160/1 85 0.7 Isopropyl oxitol acetate 58.15 Cyclohexanone 9.07 Silicone fluid Fl 11/300 0.30 If it is desirable to apply the protective layer, there are two processes that can be used -process A or process B. The protective layer is optional depending on the level of resistance required.

Process A The protective layer is applied over the hybrid solvent/radiation-curable ink layer (printed image) without thermally drying or UV curing the hybrid solvent/radiation-curable ink layer. The protective layer is applied to the hybrid solvent/radiation-curable ink layer by screen printing through a 90.48 PW screen.

The protective layer is then thermally dried for 3 minutes at 60°C before being exposed to UV radiation. The UV radiation readily passes through the protective layer to cure the ink layer beneath.

The UV cure process is highly efficient as the top coat excludes air from the UV components thus avoiding inhibition by atmospheric oxygen.

Process B The hybrid solvent/radiation-curable ink layer is thermally dried for 3 minutes at 60°C before being UV cured. The protective layer is then applied over the image by screen printing through a 90.48 PW screen and dried at 70°C for 3 minutes to produce the composite.

Example 4

A protective layer, as detailed in Table 6, can optionally be applied to the hybrid solvent'radiation-curable ink layers of Example 2. The protective layer was prepared by mixing the components of Table 6 in the given amounts. Amounts are provided as weight percentages based on the total weight of the ink.

Table 6

Protective layer Amount Primer of TableS 95.0 Desmodur N75 (isocyanate functional crosslinker) 5.0 If it is desirable to apply the protective layer, there are two processes that can be used -process A or process B as discussed hereinabove for Example 3. The protective layer is optional depending on the level of resistance required.

Example 5

A primer based on an aqueous polyurethane dispersion was prepared by mixing the components as detailed in Table 7. Amounts are given as weight percentages based on the total weight of the primer.

Table 7

Primer Amount Radiation curable aqueous polyurethane 98.0 dispersion (Ucecoat 7655) Irgacure 2959 2.0 A primer layer of the primer was drawn down onto a substrate (220 micron gloss PVC) using a 12 micron Kbar. The primer layer was dried for 3 minutes at 60°C. It is important not to UV cure the primer layer at this stage (before inkjet printing the ink thereon) as this would render the primer layer insoluble in the DEGDEE and would not perform pinning of the ink.

The substrate was then fixed to the substrate roll of a Mimaki JV400 SUV printer loaded with hybrid solvent/radiation-curable inks as detailed in Table 2. The ink was printed over both primed and non-primed areas of the substrate.

After the initial printing process, the print was dried for 3 minutes at 60°C and then passed through a UV drier fitted with lxi 00 w/cm medium pressure mercury lamp at 25 m/minute to effect cure of both the hybrid solvent/radiation-curable ink and the primer layer.

The non-primed and primed areas of the hybrid UV solvent print on 220 micron PVC were evaluated.

Specifically, the drop spread and bleed were compared between primed and non-primed areas of the print using Discovery USB microscope VMS-004 supplied by Veho. Where the primer was on the surface, the pinning was excellent. The image quality was excellent; it was glossy and had excellent colour density. The print shows that the ink droplets are still well defined. In addition to this good result, this option also offers improved chemical resistance. In contrast, in non-primed areas, the print was very grainy owing to excessive ink spreading, reticulation and blending of the ink droplets. This can be seen in Figures 2 and 3, where the image quality is enhanced in the primed area of the present invention when compared to the image in the non-primed area.

Ucecoat 7655 has a high molecular weight but as the polymer is in the form of a dispersed phase in water, the viscosity is very low. The high molecular weight has significant advantages. After evaporation of water this material forms a relatively tough dry film but which is still solvent sensitive.

After UV curing the film becomes very tough and highly chemical resistant.

The chemical resistance of the composite film was checked with isopropanol alcohol. No ink removal was evident.

A more aggressive solvent was tried, namely methyl ethyl ketone (MEK). Where the ink film was on non-primed substrate the ink was removed with a few wipes, particularly so in the highlight areas with low ink coverage. However, in primed areas, the ink resisted the MEK indicating that the digital ink had penetrated into the primer layer to produce a composite film with excellent chemical resistance properties.

DEGDEE solvent resistance of uncured primer was also checked as detailed in Table 8.

Table 8

Primer Resin system Double rubs to remove under colour layer FRD1O3-7a Uncured acrylated FUD 1

Claims

Claims 1. A method of printing onto a leather or synthetic leather substrate having a primer layer obtainable by providing the substrate, depositing a primer onto the substrate to form a primer layer, wherein the primer comprises a thermoplastic resin selected from polyurethane, polymethacrylate, polyvinyl, poly(cellulose acetate butyrate), polyester, epoxy resin, hydrocarbon resin, ketone or aldehyde resin, amino resin, and copolymers and blends thereof, and water, and at least partially drying the primer; the method comprising each of the following steps in order: (i) inkjet printing a hybrid solvent/radiation-curable ink onto the primer layer to form a hybrid solvent/radiation-curable ink layer, wherein the hybrid solvent/radiation-curable ink comprises at least 50% by weight organic solvent, based on the total weight of the ink, radiation-curable material and a photoinitiator; (ii)(a) optionally depositing a protective layer onto the hybrid solvent/radiation-curable ink layer, wherein the protective layer comprises: a thermoplastic resin selected from polyurethane, polymethacrylate, polyvinyl, poly(cellulose acetate butyrate), polyester, epoxy resin, hydrocarbon resin, ketone or aldehyde resin, amino resin, and copolymers and blends thereof, a solvent and/or radiation-curable diluent, and, when a monofunctional radiation-curable diluent is present, a photoinitiator, and a crosslinking agent; and (b) drying and curing the hybrid solvent/radiation-curable ink layer; wherein when (ii)(a) is present, (ii)(a) and (ii)(b) can be in either order, with the proviso that when step (ii)(b) occurs before step (ii)(a), the method further comprises the step of drying and/or curing the protective layer.
2. A method of printing onto a leather or synthetic leather substrate comprising each of the following steps in order: (i) providing the substrate; (ii) depositing a primer onto the substrate to form a primer layer, wherein the primer comprises: a thermoplastic resin selected from polyurethane, polymethacrylate, polyvinyl, poly(cellulose acetate butyrate), polyester, epoxy resin, hydrocarbon resin, ketone or aldehyde resin, amino resin, and copolymers and blends thereof, water; (iii) at least partially drying the primer; (iv) inkjet printing a hybrid solvent/radiation-curable ink onto the primer layer to form a hybrid solvent/radiation-curable ink layer, wherein the hybrid solvent/radiation-curable ink comprises at least 50% by weight organic solvent, based on the total weight of the ink, radiation-curable material and a photoinitiator; (v)(a) optionally depositing a protective layer onto the hybrid solvent/radiation-curable ink layer, wherein the protective layer comprises: a thermoplastic resin selected from polyurethane, polymethacrylate, polyvinyl, poly(cellulose acetate butyrate), polyester, epoxy resin, hydrocarbon resin, ketone or aldehyde resin, amino resin, and copolymers and blends thereof, a solvent and/or radiation-curable diluent, and, when a monofunctional radiation-curable diluent is present, a photoinitiator, and a crosslinking agent; and (b) drying and curing the hybrid solvent/radiation-curable ink layer; wherein when (v)(a) is present, (v)(a) and (v)(b) can be in either order, with the proviso that when step (v)(b) occurs before step (v)(a), the method further comprises step of drying and/or curing the protective layer.
3. A method according to claims 1 or 2, wherein the primer comprises polyurethane and polyurethane copolymers
4. A method according to any preceding claim, wherein the primer layer has a thickness of 40 microns or less based on the dry film thickness.
5. A method according to any preceding claim, wherein the hybrid solvent/radiation-curable ink further comprises a colorant.
6. A method according to any preceding claim, wherein the protective layer comprises polyurethane.
7. A method according to any preceding claim, wherein the primer layer is deposited onto the substrate by screen printing, flexographic printing, inkjet printing, bar coating orwipe on by hand.
8. A method according to any preceding claim, wherein the substrate is sportswear or sports equipment.
9. A printed substrate obtainable by the method of claims ito 7.