Method and apparatus for generating a superficial structure

20210187823 · 2021-06-24

    Inventors

    Cpc classification

    International classification

    Abstract

    A method and related apparatus for generating a surface structure includes the steps of: (A) applying a resin A on the surface of a material; (B) applying a liquid B on at least one portion of the resin A, when the resin A is liquid or partially solidified; (C) polymerizing, also separately, the resin A and the liquid B; and (D) removing the polymerized liquid B.

    Claims

    1. A method for making a three-dimensional surface on a substrate, comprising the steps of: (A) applying a resin A on a surface of a material, or applying an ink or varnish containing the resin A; (B) applying a liquid B on at least one portion of the resin A, when the resin A is liquid or partially solidified; (C) polymerizing, separately, the resin A and the liquid B; and (D) optionally, mechanically removing the polymerized liquid B.

    2. The method according to claim 1, wherein the resin A is selected from the group consisting of cationic photo-crosslinking resins, radical photo-crosslinking resins, epoxy resins, polyurethane resins, acrylic resins, polyester resins, and mixtures thereof.

    3. The method according to claim 1, wherein which the resin A is solid at ambient temperature and is hot-melt applied to make the resin A liquid.

    4. The method according to claim 1, wherein the liquid B is constituted by a photo-crosslinking monomer, a photo-crosslinking oligomer, or a mixture thereof.

    5. The method according to claim 1, wherein the liquid B is constituted by water.

    6. The method according to claim 1, wherein the liquid B is dispersible, emulsifiable, or soluble in water.

    7. The method according to claim 1, wherein the liquid B contains at least one substance selected from the group consisting of water, solvents, surface tension modifiers, acrylic resins, photo-crosslinking resins, photo-initiators, slip agents, wetting agents, oils, light stabilizers, antioxidants, defoamers, humectants, biocides, colorants, loadings, pigments, and mixtures thereof.

    8. The method according to claim 1, wherein the liquid B contains at least one polymerization inhibitor.

    9. The method according to claim 8, wherein the polymerization inhibitor is selected from the group consisting of UV absorbers, stereo-hindered amines (HALS); antioxidants (AO), and stabilizers.

    10. The method according to claim 1, wherein the liquid B has a surface tension higher than the resin A.

    11. The method according to claim 1, wherein a polymerized mixture of the resin A and the liquid B is softer or more brittle than the polymerized resin A.

    12. The method according to claim 1, wherein a polymerized mixture of the resin A and the liquid B has one or both the following characteristics: T.sub.g<20° C., or T.sub.g lower than the resin A.

    13. The method according to claim 1, wherein the polymerized liquid B is mechanically removed by a brushing machine or a rusticating machine.

    14. The method according to claim 1, wherein the polymerized liquid B is removed by a compressed air jet or by a high pressure water jet.

    15. The method according to claim 1, wherein the liquid B is applied by an inkjet head.

    16. The method according to claim 1, wherein the liquid B is applied in two or more separate steps by using different inkjet printing systems.

    17. The method according to claim 1, wherein polymerizations of the resin A and the liquid B occur separately.

    18. The method according to claim 1, further comprising the step, after removal of the liquid B, of applying a varnish on the surface that has become embossed so as to provide further protection or to optimize gloss of the surface.

    19. The method according to claim 1, further comprising the step of making or coating floors, furniture or architectural surfaces with the method.

    20. The method according to claim 1, further comprising the step of embossing a mold or embossing a paper for generating three-dimensional surfaces with the method.

    21. The method according to claim 1, further comprising the step of producing surfaces for microfluid sensors with the method.

    22. An apparatus for production of a three-dimensional surface on a substrate with a method according to claim 1, comprising: one or more inkjet printing systems; a mobile photo-polymerization system configured to be placed adjacently to an application of the liquid B; a photo-polymerization system; and a system for mechanically removing the polymerized liquid B.

    Description

    BRIEF DESCRIPTION OF THE DRAWINGS

    [0039] FIG. 1 depicts two schematic reproductions of steps A)-D) of the process of the invention.

    [0040] FIG. 2 depicts an embodiment of an apparatus for reproducing the method object of the invention;

    [0041] FIG. 3 shows an enlarged example and a perspective view of a “punctured” structure obtained by projecting water droplets with the aid of an inkjet application technique on the resin A not yet polymerized or partially polymerized. On the right side a measurement table of the areas comprising the holes is shown, whereas on the left a plot of the size of the areas of said holes is shown.

    [0042] FIG. 4 shows the example of FIG. 3 after the step of removing the material of the area subjected to projection of the particles of the embossing liquid has been carried out.

    DETAILED DESCRIPTION OF THE INVENTION

    [0043] According to an aspect, the present invention relates to a method for making a three-dimensional coating embossed on a substrate, comprising the steps of:

    [0044] A) applying a resin A or a varnish or ink containing it on the surface of a substrate (FIG. 2-1) thus forming a coating (FIG. 2-2);

    [0045] B) applying a liquid B on at least one portion of the resin A (FIG. 2-3);

    [0046] C) polymerizing/solidifying, also separately, the resin A and the liquid B (FIGS. 2-4 and FIGS. 2-5);

    [0047] D) removing the polymerized/solidified liquid B (FIG. 2-6).

    [0048] In the following paragraphs the term polymerized and/or solidified will be used indistinctly to identify that, at the end of the process, a solid product will be obtained.

    [0049] The method of the invention takes advantage of the different hardness of the materials applied in order to then remove the one that is more brittle, leaving the more tenacious material unchanged.

    [0050] Typically, the resin A can have various chemical nature, such as for example, but not limited to, a polyurethane, epoxy, photo-crosslinking, acrylated, acrylic resin.

    [0051] Preferably, the resin A is constituted by 100% solid in order to maximize the layer that can be embossed and frustrate the effect of the liquid B due to the evaporation of any solvent and/or water. On the other hand, for application needs the resin A could contain water and/or solvent, typically between 5% and 30%.

    [0052] In a preferred embodiment of the invention, the resin A has a photo-crosslinking nature such as for example described in the text “Radiation Curing: Science and Technology” (Pappas).

    [0053] The photo-crosslinking resins have in common the fact of polymerizing and hardening thanks to the energy irradiated by the ultraviolet ray devices and/or by irradiation with EB (Electron Beam) and are divided in two types based on the cross-linking mechanism: 1) radical resins, typically from vinyl monomers and acrylate resins that are divided in different subcategories: epoxy-acrylate, urethane-acrylate, polyester-acrylate, polyether-acrylate, amino-acrylate, silicon-acrylate, polyisoprene-acrylate, polybutadiene acrylate and acrylate monomers. Among the vinyl monomers can be cited N-vinyl caprolactame (NVC), acryloyl morpholine (ACMO), diethylene glycol divinyl ether (DVE-2), triethylene glycol divinyl ether (DVE-3) and mixtures thereof.

    [0054] By the term acrylate both acrylate and methacrylate resins are meant.

    [0055] 2) cationic resin such as epoxy resin, polyols and monomers such as oxetanes and vinyl ethers.

    [0056] The Applicant further unexpectedly found that, by varying the surface tension of liquid B and resin A, it is possible for the liquid B to more or less penetrate into the resin A and thereby modify the three-dimensional structure obtained after removing the polymerized liquid B.

    [0057] In general, the more marked the difference of surface tension between the liquid B and the resin A, the higher the corresponding embossing effect.

    [0058] The surface tension of the liquid B and the resin A can be modulated both by selecting the chemical nature of their base raw materials and by adding specific additives. For example, resins containing polar groups as hydroxyl, amines and aromatic groups will have a surface tension higher than resins containing linear structures of hydrocarbon type.

    [0059] By way of example, regarding the choice of the raw materials, in the table below the surface tension of the more common photo-crosslinking monomers is shown:

    TABLE-US-00001 SURFACE TENSION mN/m PRODUCT (25° C.) g ° C. Isobornyl acrylate 32 0 Isodecyl acrylate 24 60 2-(2-ethoxyethoxy)ethyl 30 53 acrylate Hexanediol diacrylate 36 3 Dipropylene glycol 34 04 diacrylate PEG300DA 42 8

    [0060] For what relates to the use of additives: [0061] Additives reducing the surface tension: silicones, polyether silicones, acrylate silicones, polyether silicones acrylates, fluorinated surfactants, alkoxylated alcohols. Such compounds are easily available on the market, for example commercialized by BYK (BYK-UV) and EVONIK (Tego Rad, Tego Wet, Tego Glide). [0062] Additives increasing the surface tension: amines, polyethers macromers-modified polyacrylates, silicon and polyethers macromers-modified polyacrylates. Such compounds are easily available on the market, for example commercialized by BYK (BYK 3560, BYK 3565).

    [0063] Typically, the additives are added between 0.01 and 20%, or better between 0.01 and 10%, or better between 0.01 and 2%.

    [0064] In preferred embodiment of the invention, the resin A can be in the form of hot-melt, such as Henkel-Technomelt.

    [0065] In another embodiment of the invention, the resin A can be constituted by non-photo-crosslinking materials such as polyurethane, epoxy, PLASTISOL, hot-melt (such as Kleiberit-Hotcoating) resins.

    [0066] Among the non-photo-crosslinking systems, PLASTISOL is of great interest being a mixture of PVC, plasticizers, additives and possibly solvents. PLASTISOL is commonly used as wear layer on PVC floorings such as for example LVT (Luxury Vinyl Tile). PLASTISOL is applied as a liquid, at about 150-500 g/m.sup.2 and then solidified by a thermal process at 180-200° C. for 2-4 minutes.

    [0067] In a preferred embodiment of the invention, the resin A is commonly used for protecting the floors and furniture surfaces from wear, scratches and abrasion, comprises one or more photo-crosslinking resins, photo-initiators and can contain loadings, such as for example aluminum oxide (corundum) to increase the abrasion resistance, talc for modifying its rheology, silica for reducing its brilliancy, calcium carbonate as filler loading, pigments to impart color, additives such as for example leveling agents, wetting agents, slip agents, rheology modifiers. The formulation of the photo-crosslinking resin can contain rheology modifiers, such as thixotropic agents having the function of better maintaining the shape of the embossing, both in terms of depth and definition.

    [0068] In a preferred embodiment the liquid B is immiscible o partially miscible in the resin A and, once polymerized, is mechanically removed from the resin A. Thereby the liquid B has the only function of creating the three-dimensionality without altering the chemical-physical properties of the resin A. The polymerized liquid B is more brittle than the polymerized resin A and thereby can be mechanically removed from the resin A without damaging it. Consequently, if the resin A will mainly be of apolar nature, the liquid B will preferably be polar and vice versa.

    [0069] In a preferred embodiment of the invention the liquid B, in its majority, is constituted by a photo-crosslinking resin. To be applied by ink-jetting, the liquid B must have viscosity of 10-15 cps at the shooting temperature (40-50° C.). Consequently, similarly to other formulations (varnishes and inks) photo-crosslinkable by inkjet printing, the liquid B will be mainly formed by (meth)acrylate and/or vinyl monomers. On the other hand, in order to control the rheology and reach the desired degree of hardness, in addition to the monomers, the liquid B could also contain acrylate oligomers.

    [0070] In order to obtain a brittle and easily removable formulation, ingredients characterized by low Tg can be used, such as isodecyl-acrylate, 2-(2-ethoxyethoxy) ethyl acrylate, octyl-decyl-acrylate, tri-decyl-acrylate, laurylacrylate, diacrylate polyethylene glycols of various molecular weight (200, 300, 400, 600 Dalton),

    [0071] In a further preferred embodiment of the invention, the liquid B has sufficiently high surface tension, with respect to the resin A, so as to penetrate into the resin A while maintaining the shape and thereby creating detailed structures. If on the contrary the surface tension of the liquid B were too low with respect to that of the resin A, there would be a loss of definition, having as a result the fact that the liquid B will wet the surface of the resin A.

    [0072] In a preferred embodiment of the invention, the liquid B is able to quickly penetrate and effectively mix with the resin A.

    [0073] In another further preferred embodiment of the invention, the liquid B is able to quickly penetrate and not mix or partially mix with the resin A.

    [0074] In a preferred embodiment of the invention, the liquid B contains a substance adapted to inhibit the polymerization of the resin A, thereby, after the polymerization, the areas printed with the liquid B will be more brittle than the resin A. For example, if the resin A is constituted by photo-crosslinking resins, the liquid B can contain polymerization inhibitors such as UV absorbers for example 2-hydroxyphenyl-benzophenones (BP), 2-(2-hydroxyphenyl)-benzotriazoles (BTZ) and 2-hydroxyphenyl-s-triazines (HPT); stereo-hindered amines (HALS) for example 2,2,6,6-tetramethyl piperidines (TMP); antioxidants (AO) for example sterically hindered phenols, secondary thioethers, phosphites, stabilizers (in-can stabilizer) for example quinone methide, radical scavengers.

    [0075] In a further embodiment of the invention, the liquid B once polymerized has a Tg (Tg defined as the glass transition temperature) lower than the resin A and, consequently, the areas printed with the liquid B will be easier to be removed than the polymerized resin A.

    [0076] In some embodiments, the liquid B contains additives which serve to modify properties such as the rheology and/or printability and/or color and can comprise photo-initiators, leveling agents, oils, light stabilizers, antioxidants, biocides, pigments, rheology modifiers, humectants, defoamers and mixtures thereof.

    [0077] In a preferred embodiment of the invention the liquid B has a surface tension higher than the resin A.

    [0078] Similarly to the resin A, the surface tension of the liquid B can be modulated both by selecting raw materials and by using additives, the same described above to modify the resin A.

    [0079] In addition to modifying the surface tension to obtain more or less marked penetration effects, the addition of surface tension modifiers contributes to improve the printability of the liquid B, especially when using inkjet printers.

    [0080] The control of the depth of the liquid B in the resin A can be modulated in a different way: [0081] by applying more liquid B [0082] by making more or less time passing between the application of the liquid B and the subsequent polymerization of the resin A and liquid B. [0083] by varying the speed of the droplet of the liquid B by using the waveform, where the quicker droplets will be able to sink deeper into the resin A.

    [0084] Preferably, the liquid B has low viscosity and high solvent power towards the resin A. For example, the following monomers are listed as a function of the degree of solvent power: EOEOEA>THFA>HDDA>DPGDA.

    [0085] The substrate usable in the method of the invention can be a material of different nature such as wood and derivative products for example MDF, HDF, particleboard, multi-layer wood, cellulose-based materials such as paper or cardboard, metals, plastic material (PVC, polyester, polyolefins), stone, glass, ceramic and compounds thereof.

    [0086] The substrate is selected depending on the application of the method of the invention, for example for coating of furniture, floors, shutters and frames, profiles.

    [0087] The substrate can have variable thickness depending on the application, for example in the case of decorative panels for furniture it is commonly between 8 and 20 mm whereas for the production of floors thicknesses between 2 and 6 mm are used. The method of the invention can also be used for creating structures over films, normally plastic or paper films, which are normally used for the coating and decoration of furniture and other furnishing surfaces.

    [0088] The resin A which covers the substrate has variable thickness. By way of example, the resin A can have a thickness in the range of 1-500μ equivalent to 1-500 g/m.sup.2 when the density of the resin A is 1 g/ml. Typically, to protect high-traffic flooring, grammage in the order of 80-120 g/m.sup.2 are used. Obviously, nothing prevents higher quantities from being applied with the only purpose of obtaining deeper structures.

    [0089] In an embodiment of the invention, the resin A has a thickness from 1 to 200μ, from 2 to 100μ, from 3 to 50μ, in the portion lacking the embossing and a thickness in the range of 0.05 to 100μ, from 0.5 to 50μ, from 1 to 25μ, in the embossed areas.

    [0090] The process of the invention and the equipment for its realization will be more evident from the following description wherein the embodiments depicted in the attached FIGS. 1, 2 e 3 are referred to.

    [0091] According to some embodiments, the resin A or varnish or ink to be embossed containing it, can be applied on the substrate with digital technology, for example, as depicted in FIG. 2 at point 3, by using the inkjet printing or else with the conventional techniques in use, such as roller/spray/curtain/die coating/slot-die.

    [0092] In an embodiment of the invention, the resin A is a photo-crosslinking printing varnish and/or a photo-crosslinking printing ink applied by digital printing.

    [0093] In some embodiments of the invention, the application of the liquid B occurs on the non-solidified resin A or varnish or ink containing it, of an underlying printed image.

    [0094] Typically, the photo-polymerization by UV irradiation can be carried out with one or more Hg lamps and/or LED lamps, such as for example depicted in FIG. 2 at points 4 and 5.

    [0095] According to an embodiment, the lamps are mounted on a mobile system allowing to bring them more or less close to the application system of the liquid B to better control the action of the same and thereby modulating its effect. For example, if you want to get a strong matt effect, the pre-polymerization/polymerization must occur immediately after the inkjet application, as depicted in FIG. 2, point 4.

    [0096] At the end of the process object of the invention, there will be areas constituted by the polymerized resin A and areas constituted by the polymerized liquid B. Having such areas different hardness/toughness, it could be possible to selectively mechanically remove the material that is more soft/brittle while leaving the more hard/tenacious material unchanged (FIG. 2-6).

    [0097] In another way of the invention, the liquid B is applied on the wear layer (resin A) on which the finishing is subsequently applied and consequently the mechanical removal of the polymerized liquid B.

    [0098] What has been described above is quite similar to what happens in some natural materials, such as for example wood, where in the rusticating/brushing operations, the softer part of the wood is removed, thus leaving the harder one unchanged.

    [0099] The mechanical removal of the polymerized liquid B can thus be carried out with the same machines used for rusticating/brushing the wood. Such machines use brushes and/or pads made of more or less aggressive materials (steel, brass, nylon fibers, polyester fibers) depending on the hardness of the material to be removed and the desired degree of finishing. The above described equipment is for example produced by CEFLA (e.g. RSP4) and QUICKWOOD (e.g. CDI/300+LEV).

    [0100] The removal of the polymerized liquid B can also be carried out by air jet with high pressure or else by water jet with high pressure.

    [0101] In a further embodiment of the invention, the polymerized liquid B can be removed by using an adhesive roller or tape which, once applied on the surface of the resin A, is then taken away at the same time of the removal of the polymerized liquid B which remains attached to the adhesive itself. The adhesive roller or tape can then be cleaned from the polymerized liquid B and re-used again.

    [0102] In a further embodiment of the invention, the polymerized liquid B can be removed by using a suitable solvent.

    [0103] In a preferred embodiment of the invention, after the removal of the polymerized liquid B, a finishing varnish is applied on the surface of the resin A in order to obtain the desired appearance in terms of brightness, feel and resistance to micro-scratches (FIG. 2-7).

    [0104] In another embodiment of the invention, the application of the liquid B is carried out in two separate steps and this allows for example obtaining combined effects by using liquid B with different characteristics, such as for example the surface tension.

    [0105] Typically, the method object of the invention provides the application of the liquid B by an inkjet head.

    [0106] Inkjet printing can be both in multipass/scanning mode, wherein the image is generated with multiple passages of the head, while the material to be printed moves forward, or in singlepass mode, wherein the material to be printed only passes once under the heads which are installed at the width of the same material. Singlepass printing is used for long runs (>1000 m.sup.2/h), whereas the multipass printing used for short and medium runs (10-600 m.sup.2/h) is for sure the most common one.

    [0107] Typically, inkjet printing provides the use of one head to create and jet liquid droplets that will then form the image to be printed. By way of example, details of this type of printing can be found in the book “Fundamentals of inkjet printing: the science of inkjet and droplets” (Hoath, Stephen).

    [0108] Depending on the inkjet head used, the droplets produced can have different volume and consequently different diameters.

    [0109] By way of example, the volume of the droplet and the corresponding diameter are set forth in the following table.

    TABLE-US-00002 TABLE 1 VOLUME VOLUME VOLUME VOLUME DIAMETER Lev. 1 Lev. 2 Lev. 3 (pl) (μ) (pl) (pl) (pl) 1.5 3 1.5 3 4.5 2.4 5 2.4 4.8 7.2 3 6 3 6 9 6 13 6 12 18 10 21 10 20 30 12 25 12 24 36 30 64 30 60 90 80 170 80 160 240

    [0110] In addition to the native size of the droplet, intrinsic characteristic of the head, bigger droplets can be generated by the head itself. For example, a head capable of jetting 4 gray levels, will have a droplet smaller than 6 pl whereas the bigger one will be 18 pl.

    [0111] On the contrary of the digital embossing technologies currently existing on the market only using 1-bit printing, the method of the invention allows jetting droplets in gray-scale mode. This way the effects that can be obtained are widened with the possibility of creating different depths and, at the same time, surface micro-structures.

    [0112] Typically, the method object of the invention is advantageously used for the production of furniture and/or floors. The preparation and finishing cycle is according to the material to be decorated and the desired performance.

    [0113] For example, a typical cycle for the decoration of SPC (Stone Plastic Composite), a material currently in vogue for the production of flooring, provides the following operations:

    TABLE-US-00003 TABLE 2 Operation Application ype g/m.sup.2 Notes Smoothing of Optional the substrate Adhesion primer Roller V 8/10 Optional White Roller V 20/40  One or more applications Printing primer Roller V 8/10 Optional Digital printing Roller V Adhesion primer Roller V 8/10 Optional Wear layer Roller V 40/120 One or more applications. The amount is depending on the degree of desired abrasion resistance Finishing Roller V 10/20  For the protection to scratches and for obtaining the desired degree of opacity

    [0114] The process object of the invention can be carried out both on the wear layer and on the finishing, preferably on the first one (FIG. 3).

    [0115] In order to obtain different aesthetic effects, the wear layer and the finishing can have different degrees of opacity. In fact, if the wear layer has a gloss level higher than the finishing, a glossy pore will be obtained which will consequently be highlighted.

    [0116] On the contrary, if the wear layer and finishing have the same gloss level, the pore will be less evident but with a more natural effect.

    [0117] In a further application of the invention, the method can be used for producing molds and transfer films/embossing papers. The molds for pressing melamine are generally constituted by a metal plate which is then etched mechanically and/or by corrosion thereby generating the desired structure. The process is rather laborious and long and lasts for several weeks. The molds are then subjected to chromium plating, a harmful operation for the environment that should be banned in the near future.

    [0118] On the other hand, the melamine pressing requires high temperature (160-180° C.) and pressure (15-70 bars) conditions, characteristics that often cannot be adjusted with the chemical-physical properties of the polymerized inkjet formulations. With the method of the invention a suitable resin A can be chosen instead, capable of resisting to the pressing conditions, and creating the negative of the structure which we will want to achieve after the pressing process. Similarly to the molds for the melamine pressing, the method of the invention can be used for producing molds for pressing ceramic, leather and plastics. In addition to the production of flat molds, the method of the invention can be used for the production of etching cylinders which have the same function of the molds but are mainly used on flexible materials.

    [0119] Advantageously, the application of small droplets can be used to generate microgrooves and micro-wells of a few microns in size, typical of microfluidics, for producing sensors and functional devices.

    [0120] A further application of the small droplets is to generate micro-structures which make the surface of the embossed varnish/resin/ink matt. With the latter application you can get simultaneously glossy and matt surfaces with interesting aesthetic effects.

    [0121] In another embodiment of the invention, the resin A can contain blowing agents in order to achieve high embossing volumes, but by limiting the weight of the embossed layer and/or the cost. Typically, it is possible to use hollow polymeric microspheres filled with gas, which increase the volume at given temperatures, for example EXPANCELs can be used. The expansion phase preferably occurs before applying the liquid B.

    [0122] In addition to reproducing natural materials, such as wood and stones, the method object of the invention can also be used to generate three-dimensional structures typical of graphics and/or decorative fields.

    [0123] Advantageously, the method object of the invention can be used to emboss surfaces printed in the traditional manner (rotogravure/flexo/offset).

    [0124] The following embodiment examples are provided for illustrative purposes only of the present invention and are not to be understood as limiting with regard to the scope of protection defined by the claims annexed.

    Example 1

    [0125] The liquid B is poorly miscible with the resin A and the liquid B has low Tg once polymerized.

    [0126] To a support made of melamine paper, 75μ of a photo-crosslinking varnish have been applied with a manual tool for spreading the film TEKNOS UVILUX 143-001 (resin A) for finishing floors.

    [0127] Subsequently, on the still liquid varnish, by inkjet printer of single-pass type, it has been applied the liquid B constituted by: [0128] Water: 47.5% [0129] Di-acrylate monomer PEG600DA: 47.5% [0130] Photo-initiator, TPO-L 5%

    [0131] The support has been then immediately irradiated with a PHOSEON FIRELINE lamp at 395 nm and 8 W/cm.sup.2 and subsequently with a Hg lamp at medium pressure DR. Hanle of 160 w/cm to complete the polymerization of the resin A and liquid B.

    [0132] After the application the surface appears homogeneous and the areas printed with the liquid B are evident to the naked eye.

    [0133] While with a 2H pencil it is possible to remove the areas printed with the liquid B, it is not possible to remove the polymerized resin A. Thereby the three-dimensionality is created in the areas printed with the liquid B.

    Example 2

    [0134] The liquid B is miscible with the resin A and once it is polymerized, the mixture of resin A and liquid B has low Tg.

    [0135] To a support made of melamine paper, 75μ of a photo-crosslinking varnish have been applied with a manual tool for spreading the film TEKNOS UVILUX 143-001 (resin A) for finishing floors.

    [0136] Subsequently, on the still liquid varnish, by inkjet printer of single-pass type, it has been applied the liquid B constituted by: [0137] Mono-acrylate monomer EOEOEA: 100%

    [0138] The support has been then immediately irradiated with a PHOSEON FIRELINE lamp at 395 nm and 8 W/cm.sup.2 and subsequently with a Hg lamp at medium pressure DR. Hanle of 160 w/cm to complete the polymerization of the resin A and liquid B.

    [0139] After the application the surface appears homogeneous and the areas printed with the liquid B are evident to the naked eye.

    [0140] While with a 2H pencil it is possible to remove the areas printed with the liquid B, it is not possible to remove the polymerized resin A. Thereby the three-dimensionality is created in the areas printed with the liquid B.

    Example 3

    [0141] The liquid B contains UV polymerization inhibitors and is miscible with the resin A.

    [0142] To a support made of melamine paper, 75μ of a photo-crosslinking varnish have been applied with a manual tool for stretching the film TEKNOS UVILUX 143-001 (resin A) for finishing floors.

    [0143] Subsequently, on the still liquid varnish, by inkjet printer of single-pass type, it has been applied the liquid B constituted by: [0144] Di-acrylate monomer DPGDA: 90% [0145] Tinuvin 123: 10%

    [0146] The support has been then immediately irradiated with a PHOSEON FIRELINE lamp at 395 nm and 8 W/cm.sup.2 and subsequently with a Hg lamp at medium pressure DR. Hanle of 160 w/cm to complete the polymerization of the resin A and liquid B.

    [0147] After the application the surface appears homogeneous and the areas printed with the liquid B are evident to the naked eye.

    [0148] While with a 2H pencil it is possible to remove the areas printed with the liquid B, it is not possible to remove the polymerized resin A. Thereby the three-dimensionality is created in the areas printed with the liquid B.

    Example 4

    [0149] The liquid B is immiscible with the resin A.

    [0150] To a support made of melamine paper, 75μ of a photo-crosslinking varnish have been applied with a manual tool for stretching the film TEKNOS UVILUX 143-001 (resin A) for finishing floors.

    [0151] Subsequently, on the still liquid varnish, the liquid B constituted by water has been applied by inkjet printer of the single-pass type.

    [0152] The support has been then immediately irradiated with a PHOSEON FIRELINE lamp at 395 nm and 8 W/cm.sup.2 and subsequently with a Hg lamp at medium pressure DR. Hanle of 160 w/cm to complete the polymerization of the resin A.

    [0153] After the application the surface appears homogeneous and the areas printed with the liquid B are evident to the naked eye.

    [0154] While with a 2H pencil it is possible to remove the areas printed with the liquid B, it is not possible to remove the polymerized resin A. Thereby the three-dimensionality is created in the areas printed with the liquid B.

    Example 5

    [0155] A SPC panel has been subjected to the cycle described in Table 2.

    [0156] The printer used (BARBERAN-JETMASTER) was equipped with SEIKO heads, whereas the printed image was obtained by a three-dimensional scan, carried out with a scanner (METIS), of a natural durmast veneer. The image was then uploaded in the printer by the dedicated software (RIP).

    [0157] The line speed was 18 m/min.

    [0158] After the digital printing 20 g/m.sup.2 wear layer, which was then gelled, have been applied by roller.

    [0159] Subsequently, 100 g/m.sup.2 wear layer (resin A), still in the liquid form, has been applied, to which has been applied by inkjet printer of the single-pass type the liquid B constituted by: [0160] Di-acrylate monomer DPGDA: 90% [0161] Tinuvin 123: 10%

    [0162] The panel has then been passed in a QUICKWOOD CDI/300 brushing machine equipped with 3 groups of steel brushes with wire having a diameter of 0.3 mm.

    [0163] Subsequently, 10 g/m.sup.2 matt finish varnish (6 gloss) polymerized with Hg lamps has been applied.

    [0164] The three-dimensional structure is well defined and detailed, very similar to the scanned natural material.

    [0165] The structure was then analyzed by laser profilometer analysis (3D profiler—USA), which gives a maximum depth of the structure of 95μ.

    Example 6

    [0166] To a support material (SPC), 100 g/m.sup.2 PLASTISOL formulation (resin A) for LVT floor protection has been applied by roller.

    [0167] Subsequently, the support has been passed under an inkjet printer of the single-pass type with which has been applied the liquid B constituted by: [0168] Water: 47.5% [0169] Diacrylate monomer: PEG600DA: 47.5% [0170] Photo-initiator, TPO-L 5%

    [0171] Subsequently, the panel was irradiated with ultraviolet light generated by a 160 w/cm Hg lamp at medium pressure for the polymerization of liquid B.

    [0172] The panel has then been heated in oven at 180° C. for 3′ in order to polymerize the PLASTISOL.

    [0173] The panel has then been passed in a QUICKWOOD CDI/300 brushing machine equipped with 3 groups of steel brushes with wire having a diameter of 0.3 mm.

    [0174] Subsequently, 10 g/m.sup.2 matt finish varnish (6 gloss) polymerized with Hg lamps has been applied.

    [0175] The three-dimensional structure is well defined and detailed.

    Example 7

    [0176] To a 400×400×3 mm C40 steel plate has been applied by slot-die (OSSILA), 300μ varnish (resin A) constituted as follows: [0177] CN112C60: 90% [0178] OMNICURE 184: 5% [0179] OMNICURE TPO: 0.2%

    [0180] Subsequently, the plate has been printed with a single-pass inkjet printer, the liquid B was constituted as follows: [0181] Di-acrylate monomer DPGDA: 90% [0182] Tinuvin 123: 10%

    [0183] Subsequently, the plate has been passed under a Hg lamp (160 w/cm) at the speed of 12 m/min, the varnish (resin A) is hard to the touch.

    [0184] On the surface the grain of the printed wood is evident.

    [0185] The plate has then been passed in a QUICKWOOD CDI/300 brushing machine equipped with 3 groups of steel brushes with wire having a diameter of 0.3 mm.

    [0186] The three-dimensional structure is well defined and detailed.

    [0187] The plate with the structure has been used in a compression press wherein a 400×400×8 mm MDF panel was loaded on which a kraft paper impregnated with urea-formaldehyde resin was placed, on which a decorative paper impregnated with melamine-formaldehyde resin was placed and above the latter a melamine overlay was placed. Everything has been pressed for 30″ at 180° C. and at a pressure of 20 bars.

    [0188] At the end of EXAMPLE 7

    [0189] To a support made of melamine paper, 75μ photo-crosslinking varnish for the floors finishing (TEKNOS UVILUX 143-001) has been applied with a manual film spreader.

    [0190] Subsequently, the panel has been passed under an inkjet printer of the single-pass type with which has been applied the liquid B constituted by: [0191] Diacrylate monomer, EOEOEA: 95.5% [0192] HALS, TINUVIN 123: 5%

    [0193] The support has then been immediately irradiated with a Hg lamp with medium pressure DR. 160 w/cm Hanle.

    [0194] After the application the surface appears homogeneous and the areas printed with the liquid B are evident to the naked eye.

    [0195] While with a HB pencil it is possible to remove the areas printed with the liquid B, it is not possible to remove the polymerized resin A. Thereby the three-dimensionality can be created in the areas printed with the liquid B.

    [0196] FIG. 3 shows in the central area a perspective view of a portion of a resin A layer that has been subjected to the application of water by inkjet printer. As it is evident, the central area called G has a structure with micro-holes or constituted by a plurality of small cavities that are making said area G less resistant to a mechanical removal action than the areas not subjected to the application of water and denoted by NG.

    [0197] In the plot on the left the size distribution of the micro-cavities or holes is shown and in the table on the right the measurement data are summarized.

    [0198] The removal of the residual material in the embossed areas, G i.e. in the areas bombarded by water droplets generated by inkjet printing technology, is carried out after the polymerization step. The embossed areas are weaker and less resistant to the removal action than the non-treated areas.

    [0199] FIG. 4 shows the example of FIG. 3 after the step of removing the material of the area subjected to projection of the particles of the embossing liquid has been carried out. As it is evident, a recess is formed with relatively sharp and precise, i.e. slightly jagged, side boundary walls.