METHOD FOR MANUFACTURING INKJET PRINTABLE PAPER OR FOIL FOR USE AS A DECOR PAPER OR FOIL
20210146710 · 2021-05-20
Assignee
Inventors
Cpc classification
B41M5/5218
PERFORMING OPERATIONS; TRANSPORTING
B44C5/04
PERFORMING OPERATIONS; TRANSPORTING
B41M5/5254
PERFORMING OPERATIONS; TRANSPORTING
B41M5/5245
PERFORMING OPERATIONS; TRANSPORTING
B41M5/5236
PERFORMING OPERATIONS; TRANSPORTING
International classification
B41M5/50
PERFORMING OPERATIONS; TRANSPORTING
Abstract
A method is provided for manufacturing a paper or a thermoplastic foil or a vitrimeric foil printable with an inkjet printer for use as a decor paper, respectively a decor foil in a laminate or laminated panel. The method may involve providing a paper layer, respectively a foil. At least one side of the paper layer, respectively of the foil, may be coated with an inkjet receiver coating that includes at least pigment and binder. The inkjet receiver coating may include an ink reactive compound. The papers and foils may be provided with a printed pattern and used as a decor in the panels.
Claims
1. A method for manufacturing a paper or a thermoplastic foil or a vitrimeric foil printable with an inkjet printer for use as a decor paper, respectively a decor foil, in a laminate panel, the method comprising: providing a paper layer, respectively a thermoplastic or vitrimeric foil; and coating at least one side of the paper layer, respectively of the foil, with an inkjet receiver coating that includes pigment and binder; wherein the inkjet receiver coating includes an ink reactive compound.
2. The method according to claim 1, wherein the ink reactive compound comprises a polyionic polymer.
3. The method according to claim 1, wherein the ink reactive compound comprises a substance altering the pH of the inkjet receiver coating.
4. The method according to claim 3, wherein the substance is chosen from the group consisting of formic acid, tartaric acid, acetic acid, hydrochloric acid, citric acid, phosphoric acid, sulfuric acid, AlCl.sub.3 and boronic acid.
5. The method according to claim 1, wherein the ink reactive compound comprises a metal salt.
6. The method according to claim 5, wherein the metal salt is chosen from the group consisting of CaCl.sub.2, MgCl2, CaBr, MgBr.sub.2, CMA (calcium magnesium acetate), NH.sub.4Cl, Calcium Acetate, ZrCl.sub.4 and magnesium acetate.
7. The method according to claim 1, wherein the ink reactive compound comprises a flocculating agent.
8. The method according to claim 7, wherein the flocculating agent is chosen from the group consisting of sodiumaluminate, a double sulphate salt, polyaluminumchloride, polyacrylate, dicyandiamide and polyacrylamide.
9. The method according to claim 1, wherein coating with the inkjet receiver coating involves applying a first layer of a first composition, and subsequently applying a second layer of a second composition; wherein the first and the second compositions include the binder.
10. The method according to claim 9, wherein the first layer and the second layer differ in that they show one or more of the following properties: the property that the first layer and the second layer comprise pigment and binder in a different pigment to binder ratio; the property that the dry weight of material applied for the first layer and the second layer is different; the property that the first layer and the second layer comprise pigment and binder, wherein the average particle size of the pigments contained in the first layer is larger than the average particle size of the pigments contained in the second layer; the property that the first layer and the second layer comprise an ink reactive compound in a different composition; the property that the second layer comprises a higher amount of the ink reactive compound than the first layer; the property that the first layer comprises pigment and binder, while the second layer is free from pigments, or at least comprises less pigment than the first layer, or comprises less than 10% of the pigment content of the first layer.
11. A method for manufacturing paper or a thermoplastic foil or a vitrimeric foil printable with an inkjet printer for use as a decor paper, respectively a decor foil, in a laminate panel, the method comprising: providing a paper layer, respectively a thermoplastic or vitrimeric foil; and coating at least one side of the paper layer, respectively of the foil, with a composition to form an inkjet receiver coating; wherein the composition has a pH of 3 or lower.
12. A paper or a foil for inkjet printing, wherein the paper or the foil has at least one side provided with an inkjet receiver coating comprising at least pigment and binder; wherein the inkjet receiver coating includes an ink reactive compound; and wherein the inkjet receiver coating has a pigment to binder ratio between 0.1/1 and 25/1.
13. The paper according to claim 12, wherein the paper or the foil comprises from 0.2 to 10 g/m.sup.2 dry coating weight of the ink reactive compound.
14. The paper according to claim 12, wherein the paper or the foil comprises from 0.2 to 10 g/m.sup.2 dry coating weight of pigment.
15. The paper according to claim 12, wherein the paper or the foil shows one or more of the following properties: the paper or the foil has a surface substantially formed by the binder and/or the ink reactive compound; the paper or the foil is provided with pigment in an amount having a particle surface area between 100 and 16000 m.sup.2 surface of pigment/m.sup.2 surface of paper or foil; the paper or the foil comprises from 0.05 to 5 g/m.sup.2 dry coating weight of a crosslinking agent; the paper or the foil comprises from 0.05 to 5 g/m.sup.2 dry coating weight of a particle surface modifying agent; the paper or the foil comprises from 0.005 to 2 g/m.sup.2 dry coating weight of a wetting agent; the paper or the foil comprises from 0.005 to 2 g/m.sup.2 dry coating weight of a defoaming agent; the paper or the foil comprises from 0.005 to 2 g/m.sup.2 dry coating weight of a fungicide.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0118] With the intention of better showing the characteristics according to the invention, in the following, as an example without limitative character, an embodiment is described, with reference to the accompanying drawings, wherein:
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DESCRIPTION OF NON-LIMITING EMBODIMENTS
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[0128] It is generally noted that the dimensions of the represented paper sheet 2 and the layers 4-5 is, in the figures, drawn out of scale in order to better illustrate the invention.
[0129]
[0130]
[0131]
[0132] It is noted that
[0133]
[0134] In the example several doctor blades 21 are available for partially removing resin at the surface of the resin provided paper layer 1.
[0135] In a second step S2 the resin provided paper layer 1 is dried and its residual humidity level is brought to below 10%. In the example hot air ovens 22 are used, but alternatively other heating equipment can be used, such as microwave or infrared drying equipment.
[0136]
[0137]
[0138] The upper press plate 25 is a structured press plates that provides a relief in the melamine surface of the panel 1 during the same press treatment of the step S3, by bringing the structured surface 29 of the upper press plate 25 into contact with the melamine of the protective layer 28.
[0139]
[0140]
[0141]
[0142] After drying the inks, the printed paper layer is preferably rolled up and used in the method illustrated in
[0143] With the intention of further illustrating the invention, here below, without any limitative character, some more exemplary embodiments are listed, with reference to
EXAMPLE C
[0144] 6 kg of commercially available amorphous silica (Syloid EDS) was dispersed in 41 kg of water and heated to a temperature of 80° C. To this mixture 2.7 kg of a silane (Dynasilan), acting as a particle surface modifying agent or coupling agent, was added and let stir with for 30 minutes. Then 2.3 kg of glyoxal 40% (BASF), as a crosslinking agent, was mixed and let stir for another 30 minutes. Then 0.5 kg of boronic acid, also functioning as crosslinking agent, was added and let stir for 10 minutes.
[0145] Separately 2.5 kg of polyvinylalcohol (mowiol 20/98 Kuraray) was dissolved in 26.4 kg of water at 90° C. and left stirring until this was completely dissolved (2 hours).
[0146] Hereafter the silica dispersion was added to the mowiol solution and stirred thoroughly. To this mixture 0.04 kg of leveling agent, 0.04 kg of antifoam and 0.03 kg of fungicide was added and stirred for another 5 minutes before the coating was bottled and cooled down. The obtained coating composition is free from any ink reactive compound or ink destabilizing agent. In particular the availability of the boronic acid is not in an amount capable of lowering the pH of the ink receiver composition to pH 3 or below.
[0147] The pigment to binder ratio was 2.4/1 and the solids content was 13.5% by weight.
[0148] The coating was brought to the correct viscosity for coating with a reverse gravure roller (30 seconds din cup 4 at 23° C.) by adding water. The solids content went to 10% by weight.
[0149] On a blank paper (Technocel MPK 3723) 20 g/m.sup.2 of the coating was applied by means of a reverse gravure roller and dried.
EXAMPLE D:
[0150] 6 kg of commercially available amorphous silica (Syloid EDS) was dispersed in 41 kg of water and heated to a temperature of 80° C. To this mixture 2.7 kg of a silane (Dynasilan), acting as a particle surface modifying agent or coupling agent, was added and let stir with for 30 minutes. Then 2.3 kg of glyoxal 40% (BASF), acting as a crosslinking agent, was mixed and let stir for another 30 minutes. Then 0.5 kg of boronic acid, also acting as a crosslinking agent, was added and let stir for 10 minutes. After this 5 kg of a 40% aqueous solution of polyDADMAC (polyquat40U05 by Katpol) was added and let stir for another 10 minutes. The polyDADMAC is a polyionic polymer that functions as an ink destabilizing agent in accordance with the invention.
[0151] Separately 2.5 kg of mowiol 20/98 (Kuraray) was dissolved in 26.4 kg of water at 90° C. and left stirring until this was completely dissolved (2 hours).
[0152] Hereafter the silica dispersion was added to the mowiol solution and stirred thoroughly. To this mixture 0.04 kg of leveling agent, 0.04 kg of antifoam and 0.03 kg of fungicide was added and stirred for another 5 minutes before the coating was bottled and cooled down.
[0153] The pigment to binder ratio was 2.4/1 and the solids content was 18.5% by weight.
[0154] The coating was brought to the correct viscosity for coating with a reverse gravure roller (30 seconds din cup 4 at 23° C.) by adding water. The solid content went to 15% by weight.
[0155] On a blank paper (Technocel MPK 3723) 20 g/m.sup.2 of the coating was applied by means of a reverse gravure roller and dried.
EXAMPLE E
[0156] Two coating compositions were made.
[0157] First coating composition:
[0158] 13.4 kg of commercially available amorphous silica (Syloid EDS) was dispersed in 41 kg of water and heated to a temperature of 80° C. To this mixture 6 kg of a silane (Dynasilan) was added and let stir with for 30 minutes. Then 5.2 kg of glyoxal 40%
[0159] (BASF) was mixed and let stir for another 30 minutes. Then 0.5 kg of boronic acid was added and let stir for 10 minutes. After this 5 kg of polyquat40U05 (by Katpol) was added and let stir for another 10 minutes.
[0160] Separately 2.5 kg of mowiol 20/98 (Kuraray) was dissolved in 26.4 kg of water at 90° C. and left stirring until this was completely dissolved (2 hours).
[0161] Hereafter the silica dispersion was added to the mowiol solution and stirred thoroughly. To this mixture 0.04 kg of leveling agent, 0.04 kg of antifoam and 0.03 kg of fungicide was added and stirred for another 5 minutes before the coating was bottled and cooled down.
[0162] The pigment to binder ratio was 5.5/1 and the solids content was 26% by weight.
[0163] Second coating composition: 46 kg of the first coating composition was mixed with 54 kg of an 8% mixture of mowiol 20/98 in water.
[0164] The pigment to binder ratio of the second coating composition was 0.95/1 and the solids content was 17% by weight.
[0165] Both coating compositions were brought to the correct viscosity for application by means of reverse gravure rollers (30 seconds din cup 4 at 23° C.) by adding water. The solids content of the first coating composition was 20% by weight and the second coating composition had 11% by weight solids content.
[0166] On a blank paper (Technocel MPK 3723) the inkjet receiver coating was applied in two partial steps, wherein respectively a first layer with 12 g/m.sup.2 of the first coating composition was applied by a reverse gravure roller and then dried, and, subsequently, a second layer was applied there upon with 12 g/m.sup.2 of the second coating composition, also by means of a reverse gravure roller and then dried.
Print Proofing:
[0167] A premetered application method was used to apply ink on the treated papers of examples C to E, as well as on untreated base paper (Technocel MPK 3723), labelled as paper A, and a commercially available inkjet quality paper, labelled as paper B. The high absorption of the papers excluded Mayer bar coating. For this reason, the K printing proofer by RK printcoat instruments was used with the 100 lines/inch printing plate and a water based red digital printing ink.
[0168] The prints where then analysed by a Byk Spectro guide to measure the L, a and b value. Then the CD (color density) value was calculated by multiplying a with b and dividing this by L. All papers A to E were then ranked according to CD value, this is depicted in
[0169] From
[0170] The present invention is in no way limited to the above described embodiments, but such methods, paper layers, thermoplastic foils and vitrimeric foils may be realized according to several variants without leaving the scope of the invention.