METHOD FOR MANUFACTURING INKJET PRINTABLE PAPER OR FOIL FOR USE AS A DECOR PAPER OR FOIL
20220001685 · 2022-01-06
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
An inkjet receiver coating may be used in a method for manufacturing a paper or a thermoplastic foil that is printable with an inkjet printer. The paper or the foil may be used as a decor paper or a decor foil, respectively, in a laminate panel. The paper or the foil may be coated on at least one side with the inkjet receiver coating. The inkjet receiver coating may include at least pigment and binder, and an ink reactive compound.
Claims
1. An inkjet receiver coating for use in a method for manufacturing a paper or a thermoplastic foil that is printable with an inkjet printer, wherein the paper or the foil is for use as a decor paper or a decor foil, respectively, in a laminate panel, wherein the paper or the foil is coated on at least one side with the inkjet receiver coating, the inkjet receiver coating comprising: at least pigment and binder; and an ink reactive compound.
2. The inkjet receiver coating according to claim 1, wherein the ink reactive compound comprises a polyionic polymer.
3. The inkjet receiver coating according to claim 1, wherein the ink reactive compound comprises a substance altering the pH of the inkjet receiver coating.
4. The inkjet receiver coating according to claim 3, wherein the substance is chosen from the list consisting of formic acid, tartaric acid, acetic acid, hydrochloric acid, citric acid, phosphoric acid, sulfuric acid, AlCl.sub.3, and boronic acid.
5. The inkjet receiver coating according to claim 1, wherein the ink reactive compound comprises a metal salt.
6. The inkjet receiver coating according to claim 5, wherein the metal salt is chosen from the list consisting of CaCl.sub.2, MgCl.sub.2, CaBr, MgBr.sub.2, CMA (calcium magnesium acetate), NH.sub.4CI, Calcium Acetate, ZrCl.sub.4, and magnesium acetate.
7. The inkjet receiver coating according to claim 1, wherein the ink reactive compound comprises a flocculating agent.
8. The inkjet receiver coating according to claim 7, wherein said flocculating agent is chosen from the list consisting of sodiumaluminate, a double sulphate salt, polyaluminumchloride, polyacrylate, dicyandiamide, and polyacrylamide.
9. The inkjet receiver coating according to claim 1, wherein the inkjet receiver coating has a pigment to binder ratio between 0.1/1 and 25/1.
10. The inkjet receiver coating according to claim 1, wherein the pigments have a particle surface area between 100 and 16000 m.sup.2 surface of pigment/m.sup.2 surface of paper or foil.
11. The inkjet receiver coating according to claim 1, wherein the pigments have an average particle size of 100 nm to 20 μm.
12. The inkjet receiver coating according to claim 11, wherein the pigments have a particle size between 1-12 μm.
13. The inkjet receiver coating according to claim 1, wherein the pigments are porous inorganic pigments.
14. The inkjet receiver coating according to claim 1, wherein the pigments comprises precipitated silica, amorphous silica, and/or fumed silica.
15. The inkjet receiver coating according to claim 1, wherein the inkjet receiver coating is applied in a first layer of a first composition and, subsequently, a second layer of a second composition; and wherein the first and the second compositions include the binder.
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.
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[0132] It is noted that
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[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.
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[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.
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[0142] 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
[0143] 6 kg of commercially available amorphous silica (Syloid ED5) 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.
[0144] 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).
[0145] 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.
[0146] The pigment to binder ratio was 2.4/1 and the solids content was 13.5% by weight.
[0147] 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.
[0148] 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
[0149] 6 kg of commercially available amorphous silica (Syloid ED5) 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.
[0150] 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).
[0151] 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.
[0152] The pigment to binder ratio was 2.4/1 and the solids content was 18.5% by weight.
[0153] 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.
[0154] 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
[0155] Two coating compositions were made.
[0156] First coating composition:
[0157] 13.4 kg of commercially available amorphous silica (Syloid ED5) 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% (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.
[0158] 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).
[0159] 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.
[0160] The pigment to binder ratio was 5.5/1 and the solids content was 26% by weight.
[0161] Second Coating Composition:
[0162] 46 kg of the first coating composition was mixed with 54 kg of an 8% mixture of mowiol 20/98 in water.
[0163] The pigment to binder ratio of the second coating composition was 0.95/1 and the solids content was 17% by weight.
[0164] 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.
[0165] 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.
[0166] 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.