AU2013205626A1 - Compressible decorative paper impregnating agent which can be printed by the inkjet method - Google Patents
Compressible decorative paper impregnating agent which can be printed by the inkjet method Download PDFInfo
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- AU2013205626A1 AU2013205626A1 AU2013205626A AU2013205626A AU2013205626A1 AU 2013205626 A1 AU2013205626 A1 AU 2013205626A1 AU 2013205626 A AU2013205626 A AU 2013205626A AU 2013205626 A AU2013205626 A AU 2013205626A AU 2013205626 A1 AU2013205626 A1 AU 2013205626A1
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- paper
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- decorative paper
- decorative
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Links
- 238000000034 method Methods 0.000 title claims description 25
- 229920005989 resin Polymers 0.000 claims abstract description 51
- 239000011347 resin Substances 0.000 claims abstract description 51
- 238000001035 drying Methods 0.000 claims abstract description 15
- 239000000463 material Substances 0.000 claims abstract description 11
- 238000000576 coating method Methods 0.000 claims abstract description 9
- 239000011248 coating agent Substances 0.000 claims abstract description 7
- 239000000049 pigment Substances 0.000 claims description 22
- 239000000203 mixture Substances 0.000 claims description 19
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 9
- 238000004132 cross linking Methods 0.000 claims description 9
- 229920000877 Melamine resin Polymers 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 6
- 239000011230 binding agent Substances 0.000 claims description 4
- 229920001807 Urea-formaldehyde Polymers 0.000 claims description 3
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 claims description 3
- 229910001593 boehmite Inorganic materials 0.000 claims description 3
- FAHBNUUHRFUEAI-UHFFFAOYSA-M hydroxidooxidoaluminium Chemical compound O[Al]=O FAHBNUUHRFUEAI-UHFFFAOYSA-M 0.000 claims description 3
- 229920000642 polymer Polymers 0.000 claims description 3
- 239000000377 silicon dioxide Substances 0.000 claims description 3
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 claims description 2
- 229910021502 aluminium hydroxide Inorganic materials 0.000 claims description 2
- 239000004925 Acrylic resin Substances 0.000 claims 2
- 239000003795 chemical substances by application Substances 0.000 abstract description 2
- 239000000123 paper Substances 0.000 description 108
- 239000000976 ink Substances 0.000 description 26
- 239000001913 cellulose Substances 0.000 description 23
- 229920002678 cellulose Polymers 0.000 description 23
- 239000010410 layer Substances 0.000 description 23
- 238000007639 printing Methods 0.000 description 14
- 238000003825 pressing Methods 0.000 description 13
- 239000000975 dye Substances 0.000 description 11
- 238000012360 testing method Methods 0.000 description 11
- 238000005470 impregnation Methods 0.000 description 10
- 239000000523 sample Substances 0.000 description 9
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 7
- 230000009257 reactivity Effects 0.000 description 7
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 6
- 239000000654 additive Substances 0.000 description 6
- 239000000945 filler Substances 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- 239000000725 suspension Substances 0.000 description 6
- 239000004372 Polyvinyl alcohol Substances 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 238000000605 extraction Methods 0.000 description 4
- 230000014759 maintenance of location Effects 0.000 description 4
- 229920002451 polyvinyl alcohol Polymers 0.000 description 4
- 238000004513 sizing Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 3
- 239000002671 adjuvant Substances 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 238000004040 coloring Methods 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 239000011121 hardwood Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- 239000000057 synthetic resin Substances 0.000 description 3
- 239000000454 talc Substances 0.000 description 3
- 229910052623 talc Inorganic materials 0.000 description 3
- 239000004408 titanium dioxide Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 244000166124 Eucalyptus globulus Species 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 239000004411 aluminium Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 239000001164 aluminium sulphate Substances 0.000 description 2
- 235000011128 aluminium sulphate Nutrition 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000011093 chipboard Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000013530 defoamer Substances 0.000 description 2
- BUACSMWVFUNQET-UHFFFAOYSA-H dialuminum;trisulfate;hydrate Chemical compound O.[Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O BUACSMWVFUNQET-UHFFFAOYSA-H 0.000 description 2
- 238000007646 gravure printing Methods 0.000 description 2
- 238000007641 inkjet printing Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 239000011118 polyvinyl acetate Substances 0.000 description 2
- 229920002689 polyvinyl acetate Polymers 0.000 description 2
- 238000004537 pulping Methods 0.000 description 2
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 2
- 229940043267 rhodamine b Drugs 0.000 description 2
- 239000011122 softwood Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- PUAQLLVFLMYYJJ-UHFFFAOYSA-N 2-aminopropiophenone Chemical compound CC(N)C(=O)C1=CC=CC=C1 PUAQLLVFLMYYJJ-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000001828 Gelatine Substances 0.000 description 1
- 241000294754 Macroptilium atropurpureum Species 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000005083 Zinc sulfide Substances 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 239000005030 aluminium foil Substances 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 239000010431 corundum Substances 0.000 description 1
- 229910052593 corundum Inorganic materials 0.000 description 1
- 238000007766 curtain coating Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 150000005125 dioxazines Chemical class 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- -1 for example Polymers 0.000 description 1
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical class O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000002346 layers by function Substances 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 235000012243 magnesium silicates Nutrition 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 229910052976 metal sulfide Inorganic materials 0.000 description 1
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920000371 poly(diallyldimethylammonium chloride) polymer Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 150000004053 quinones Chemical class 0.000 description 1
- 239000013074 reference sample Substances 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Paper (AREA)
Abstract
Abstract A decorative paper impregnating agent for decorative coating materials, which can be compressed directly to form a laminate, and which is impregnated using an impregnating resin and is provided with a color receiving layer and has a residual moisture of at least 3.5% and a flow of greater than 0.4% after drying.
Description
AUSTRALIA Patents Act 1990 COMPLETE SPECIFICATION Standard Patent Applicant: TECHNOCELL DEKOR GMBH & CO. KG Invention Title: Compressible decorative paper impregnating agent which can be printed by the inkjet method The following statement is a full description of this invention, including the best method for performing it known to us: 17/06/2010 A Compressible decorative paper impregnate which can be printed by the ink jet method The invention relates to a decorative paper impregnate which is impregnated with a thermally curable impregnating resin 5 and which can be printed by means of ink jet methods, wherein after printing the impregnated decorative paper can be pressed directly with a wood material to form a laminate. Decorative papers are required for the production of 10 decorative laminates which are used as building materials in furniture manufacture and in interior finishing. Decorative laminates principally comprise so-called high-pressure laminates (HPL) and low-pressure laminates (LPL). For the production of a high-pressure laminate the decorative paper 15 in the unprinted or printed state is impregnated with a resin and is pressed with one or more layers of kraft paper sheets which have been impregnated in phenol resin (core papers) in a laminating press at a temperature of about 110 to 1700C and a pressure of 5.5 to 11 MPa. The laminate (HPL) thus formed 20 is then glued or adhered with a support material such as HDF or chipboard. A low-pressure laminate is produced by pressing the unprinted or printed decorative paper impregnated with a resin directly with the supporting board at a temperature of 160 to 2000C and a pressure of 1.25 to 3.5 MPa. 25 The finishing of the material surfaces can be of a visual nature (by appropriate colouring) and/or of a physical nature (by coating the board surface with appropriate functionality and structure). Decorative papers can be processed with or 30 without a printed-on pattern. For this purpose the printed or unprinted decorative paper is usually impregnated with 2 synthetic resins in a single-stage or multi-stage process, then dried, wherein the resin still remains reactive and is then irreversibly hot pressed with a support material into sheets or as rolled goods. The resin cures during the 5 pressing. Due to this curing not only the bond to the board is produced but the paper is completely sealed chemically and physically. The application of the printing pattern is usually 10 accomplished in a gravure printing method. Particularly during the production of printing patterns which are customary in the market, this printing technique has the advantage of printing large quantities of paper at high machine speed. 15 However, the gravure printing method should be assessed as not being cost-effective for smaller quantities and inadequate in regard to printing quality in the case of complex designs. Among the printing techniques which meet the 20 requirements for flexibility and quality, the ink jet printing method (ink jet) is acquiring increasing importance. In order to make decorative papers printable by means of ink jet, these are coated with one or several functional layers 25 to receive the inks and fix the dyes. Such a decorative paper which can be printed by the ink jet method is described in DE 199 16 546 Al. An ink-jet printable decorative paper can be impregnated with 30 thermosetting resins after printing and then hot pressed. Since the paper is frequently only printed in sheets up to several linear metres long, e.g. 3.5 metres, impregnation in MI/ca 021858Wo 17/06/2010 -3 an impregnating system is frequently not possible. In this case, the sheet is pressed between highly resin-impregnated papers. During the pressing process the resin penetrates into the decorative paper and cures. The result is a good-quality 5 laminate. Compared to an impregnating system, however, this procedure does not ensure that the decorative paper is uniformly through-impregnated. Consequently, complete sealing of the paper is not achieved in this process. 10 When pressing the decorative paper between the resin impregnated papers, it is advantageous that only the decorative paper that has been printed is pressed. If the decorative paper is printed as a roll and subsequently impregnated, losses of material occur caused by foreruns in 15 the systems, printing and cutting transitions and process adjustments. High-quality material is therefore lost. It is the object of the invention to provide a decorative paper which does not have the disadvantages described above. 20 The object is achieved by a decorative paper impregnate which contains an impregnated base paper (decorative base paper) and an ink receiving layer, wherein the base paper contains an impregnating resin in a quantity of 40 to 250% by weight 25 of the basis weight of the base paper, and after drying the decorative paper impregnate has a residual moisture of at least 3.5% by weight and a flow of more than 0.4%, measured at a pressure of 180 bar and a temperature of 143 t 2 0 C. 30 In a particular embodiment of the invention, the quantity of the impregnating resin is 80 to 125% by weight of the basis weight of the base paper. MI/ca 071858WO 17/06/2010 -4 The residual moisture of the decorative paper after drying is preferably 5 to 8.5%. 5 The effect according to the invention is achieved in particular if the decorative base paper is initially core impregnated, pre-dried and only afterwards coated with one or more ink-receiving layers in a coating process and dried. It should be noted in this case that after pre-drying the core 10 impregnated base paper and drying the finished decorative paper impregnate, the impregnating resin is not cured and therefore remains reactive. The term "not cured" in the sense of the invention means that 15 the impregnating resin has a degree of cross-linking of at most 65%, preferably of at most 30%. The method for determining the degree of cross-linking is described in detail in the further text. 20 The method for producing the decorative paper impregnate according to the invention is characterised by the following steps: (a) fabricating a decorative base paper with a basis weight of 30 to 200 g/m 2 , 25 (b) core-impregnating the decorative base paper with a thermally curable impregnating resin in a quantity of 40 to 250% by weight of the basis weight of the base paper, (c) pre-drying the core-impregnated paper, wherein the drying temperature is adjusted so that the paper has a moisture of 9 30 to 20% and the resin is not cured and therefore still reactive. MI/ca 071858Wo 17/06/2010 -5 (d) Coating the pre-dried core-impregnated paper with at least one ink-receiving layer, (e) Drying the core-impregnated decorative paper provided with at least one ink-receiving layer to a residual moisture 5 of 3.5 to 8.5%, wherein the resin is cross-linked at most to a degree of cross-linking of 30% and therefore still reactive and the dried decorative paper impregnate produced has a flow of more than 0.4% measured at a pressure of 180 bar and a temperature of 143 t 2 0 C. 10 The core impregnation can be carried out off-line in a standard impregnation system or inline inside the paper machine with the aid of usual application units. 15 In a further embodiment of the invention, the ink-receiving layer can also be applied to the core-impregnated paper without pre-drying. In a further embodiment of the invention, the ink-receiving 20 layer can also be applied to a multiple impregnated resin impregnated paper (a conventional decorative paper impregnate). In a particular embodiment of the invention, the decorative 25 paper impregnate has a reactivity of 2 to 3 minutes at a temperature of 140*C and a pressure of 25 bar. The decorative paper impregnate produced in this way can be rolled up in the system or divided into sheets. The 30 decorative paper can then be printed in high quality using various ink jet methods. After the printing, the paper is hot pressed onto a wood-based board or to form a laminate in a MI/ca 071B58Wo 17/06/2010 -6 coating press. For this purpose resin-impregnated paper (underlay) as composite layer or any other adhesive layer is no longer required. However, a resin-impregnated underlay can be additionally used if desired. A resin-impregnated overlay 5 can be applied as a protective layer before pressing. However, the printed product can also be sealed first with a varnish. The decorative base papers which can be used according to the 10 invention are those which have not undergone any sizing in the mass nor any surface sizing. They substantially consist of cellulose, pigments and fillers and usual additives. Usual additives can be wet strength additives, retention aids and fixing aids. Decorative base papers differ from the usual 15 papers by the very much higher filler fraction or pigment content and the lack of any mass sizing or surface sizing which is usual in paper. Softwood cellulose, hardwood cellulose or mixtures of both 20 types of cellulose can be used to produce the decorative base papers. It is preferable to use 100% hardwood cellulose. However, mixtures of softwood/hardwood cellulose in the ratio of 5:95 to 50:50, in particular 10:90 to 30:70 can also be used. The base papers can be produced on a Fourdrinier paper 25 machine or a Yankee paper machine. For this purpose the cellulose mixture having a stock consistency of 2 to 5% by weight can be refined to a freeness of 10 to 45 0 SR. In a mixing vat fillers and/or pigments, colour pigments and/or dyes as well as wet strength additives such as 30 polyamide/polyamine epichlorohydrin resin, cationic polyacrylates, modified melamine formaldehyde resin or cationised starches can be added in the usual quantities for MI/ca 071858Wo 17/06/2010 -7 the manufacture of decorative papers and blended thoroughly with the cellulose mixture. The fillers and/or pigments can be added in a quantity of up 5 to 55% by weight, in particular 10 to 45% by weight, relative to the weight of the cellulose. Suitable pigments and fillers are, for example, titanium dioxide, talc, zinc sulphide, kaolin, aluminium oxide, calcium carbonate, corundum, aluminium and magnesium silicates or mixtures thereof. 10 The high consistency matter produced in the mixing vat can be diluted to a stock consistency of about 1%. If necessary, further adjuvants such as retention aids, defoamers, dyes and other previously named adjuvants or mixtures thereof can be 15 added. This low-consistency matter is passed via the head box of the paper machine to the wire section. A fibre fleece is formed and after dewatering the base paper is obtained which is then further dried. The basis weights of the papers produced can be 30 to 200 g/m 2 20 Depending on the application and the quality requirements, the decorative base papers used according to the invention can be constituted as follows: smooth, i.e. having a Bekk smoothness of more than 80 s, 25 unsmoothed, less than 80 s, smoothed with a Yankee cylinder or with a calender, not pre-impregnated or pre-impregnated with a synthetic resin, very air-permeable (Gurley values below 20 s/hml) or dense 30 (Gurley values above 20 s/hml) or even in the case of the pre-impregnates, extremely dense with Gurley values above 200 s/hml. MI/ca 021858WO 17/06/2010 8 The decorative paper according to the invention can be coloured. Inorganic colour pigments such as metal oxides, hydroxides and oxide hydrates, metal sulphides, sulphates, 5 chromates and molybdates or mixtures thereof, as well as organic colour pigments and/or dyes such as carbonyl colorants (e.g. quinones, quinacridone), cyanine colorants, azo colorants, azomethines and methines, phthalocyanines or dioxazines can be used for colouring. Particularly preferred 10 are mixtures of inorganic colour pigments and organic colour pigments or dyes. The quantity of the colour pigment/pigment mixture or dye/dye mixture can be 0.0001 to 5% by weight relative to the mass of cellulose depending on the type of substance. 15 All known receiving layers can be used for the ink receiving layer. In this case, these mostly comprise hydrophilic coatings containing water-soluble or water-dispersible polymers. 20 The ink receiving layer can additionally contain fillers, pigments, dye-fixing substances such as quaternary polyammonium salts and other adjuvants usually used in such layers. A suitable quaternary polyammonium salt is 25 polydiallyl dimethylammonium chloride. In a preferred embodiment of the invention the ink-receiving layer contains a pigment and a binder in a quantitative ratio of 10:90 to 90:10. The quantity of the pigment in the ink 30 receiving layer is preferably 5 to 80% by weight, but in particular 10 to 60% by weight relative to the dry weight of the layer. MI/ca 071858WO 17/06/2010 -9 The pigment can be any pigment usually used in ink jet recording materials, but in particular aluminium oxide, aluminium hydroxide, boehmite and silica (such as 5 precipitated or pyrogenically generated silica). The binder can be a water-soluble and/or water-dispersible polymer, for example, polyvinyl alcohol, polyvinyl pyrrolidone, polyvinyl acetate, starch, gelatine, 10 carboxymethyl cellulose, ethylene/vinyl acetate-copolymer, styrene/acrylic acid ester copolymers or mixtures thereof. A polyvinyl alcohol having a degree of saponification of 88 to 99% can be used as the polyvinyl alcohol. 15 In a particular embodiment of the invention, the ink receiving layer can be coloured. The colouring can be accomplished with the same colour pigments and/or dyes used to colour the base paper. The quantity (concentration) of the colour pigment and/or dye in the ink receiving layer relative 20 to the dried ink receiving layer is preferably about 45 to 75%, in particular 45 to 65% of the quantity of colour pigment and/or dye in the base paper, relative to the cellulose (atro). 25 The application weight of the ink-receiving layer can be 2 to 25 g/m 2 , in particular 3 to 20 g/m 2 , but preferably 4 to 15 g/m 2 . The ink receiving layer can be applied with the usual application methods such as roller application, slotted nozzle application, gravure or nip methods, curtain coating, 30 air brushing or metering bar. MI/ca 071858WO 17/06/2010 - 10 Suitable impregnating resins are the impregnating resins usually used in this technical field, in particular melamine formaldehyde resin, urea formaldehyde resin, phenol formaldehyde resin, polyacrylates, acrylic acid ester/styrene 5 copolymers and mixtures thereof. Particularly suitable are so-called "slow" impregnating resins which have a clouding time of more than 4.5 minutes. The clouding time is the time in which a resin at a temperature of 100*C shows a first clouding which signals the beginning of the polymerisation 10 reaction. The impregnating resin is used in a quantity of 40 to 250% by weight, preferably 80 to 125% by weight, of the basis weight of the decorative base paper. 15 EXAMPLES Example 1 20 A cellulose suspension was prepared by pulping a cellulose mixture of 80% by weight eucalyptus cellulose and 20% by weight of pine sulphate cellulose at a stock consistency of 5% to a freeness of 330 SR. This was then followed by the addition of 1.8% by weight of epichlorohydrin resin as wet 25 strength additive. This cellulose suspension was adjusted to a pH of 6.5 to 7 by means of aluminium sulphate. A mixture of 40% by weight of titanium dioxide and 5% by weight of talc, 0.11% by weight of a retention aid and 0.03% by weight of a defoamer was then added to the cellulose suspension and a 30 decorative base paper having a basis weight of 81 g/m 2 and an ash content of about 32% by weight was prepared. The weight specification relates to the cellulose. MI/ca 071858Wo 17/06/2010 - 11 In the next step a coating mixture was prepared for the ink receiving layer having the following composition: 5 Water 80% by weight Boehmite 10% by weight Polyvinyl alcohol 5% by weight Polyvinyl acetate 4% by weight Quat. polyammonium salt 1% by weight 10 The decorative base paper produced was acted upon by a "slow" resin in the first stage of a usual decorative paper impregnating system and after the penetration phase, was immersed and then only moderately squeezed so that a small 15 resin film remains on the surface of the paper, A pure melamine formaldehyde resin having a solid content of 51% and a clouding time of 4.5 minutes was used as resin, The core-impregnated paper was dried to amoisture of 12%. The 20 basis weight of the paper after impregnation was 139 g/m 2 The pre-dried core-impregnated paper was then coated with the ink jet ink receiving layer described in detail above with an application weight of 6 g/m 2 and dried to a final moisture of 25 6.3%. The dried decorative paper impregnate had a basis weight of 140 g/m 2 and a thickness of 133 pm. 30 The reactivity of the impregnating resin in the dried decorative paper impregnate was 2.5 minutes. The degree of cross-linking was 29%. MI/ca 071858WO 17/06/2010 - 12 The flow of the decorative paper impregnate according to the invention was 1.2%. 5 The decorative paper impregnate produced according to Example 1 was printed in an ink jet printer (HP 2500 with pigmented inks) and divided into DIN A4 sheets. These sheets were placed on a chipboard, covered with an overlay film (paper having a basis weight of 35 g/m 2 which was resin-impregnated 10 to 116 g/m 2 ) and hot pressed. The pressing was carried out at a temperature of 140 0 C and a pressure of 25 bar. Example 2 A cellulose suspension was prepared by pulping 100% by weight 15 eucalyptus cellulose at a stock consistency of 5% to a freeness of 330 SR. This was then followed by the addition of 1.8% by weight of epichlorohydrin resin as wet strength additive. This cellulose suspension was then adjusted to a pH of 6.5 to 7 by means of aluminium sulphate. A mixture of 36% 20 by weight of titanium dioxide and 5% by weight of talc, 0.11% by weight of a retention aid and 0.03% by weight of a defoamer was then added to the cellulose suspension and a decorative base paper having a basis weight of about 80 g/m 2 and an ash content of about 30% by weight was prepared from 25 this. The weight specification relates to the cellulose. The decorative paper produced was acted upon by a "slow" resin in the first stage of a usual decorative paper impregnating system and after the penetration phase, was 30 immersed and then only moderately squeezed (as in Example 1). The resin is a pure melamine formaldehyde resin having a solid content of 51% and a clouding time of 5.5 minutes. The MI/ca 071858WO 17/06/2010 - 13 core-impregnated paper was dried to amoisture of 13%. The basis weight of the paper after impregnation was 162 g/m2 The pre-dried core-impregnated paper was then coated with the 5 ink jet ink receiving layer described in detail above with an application weight of 7 g/m 2 and dried to afinal moisture of 6.5%. The dried decorative paper impregnate had a basis weight of 10 160 g/m and a thickness of 149 pm. The reactivity of the impregnating resin in the dried decorative paper impregnate was 3.5 minutes. The degree of cross-linking was 26%. The flow of the decorative paper impregnate was 1.5%. 15 The decorative paper impregnate according to Example 2 was printed in an ink jet printer (HP 2500 with pigmented inks) and divided into DIN A4 sheets. These sheets were placed on achipboard, covered with an overlay film as in Example 1 and hot pressed. The pressing was carried out at a temperature of 20 140*C and a pressure of 25 bar. The laminated boards produced with the aid of the decorative papers according to the invention exhibit properties of a high-quality melamine coating. They are distinguished by a 25 closed surface which is free from bubbles and discolorations in a water vapour test. The surface is also resistant to the action of chemicals in accordance with the standard EN 438 for laminated boards, 30 The following advantages are additionally associated with the procedure according to the invention: MI/ca 071859Wo 17/06/2010 - 14 - Even short web lengths of a few linear metres can be fully through-impregnated. Usually in an industrial synthetic resin impregnation at least an entire impregnating system length is used as a forerun for drawing in and monitoring the settings, 5 which in numbers means 50 to 100 metres. - Since the decorative paper according to the invention is only printed after the core impregnation of the paper web, the expensive and sensitive printing is not endangered by the 10 impregnation process. - When printing with aqueous printing inks, the paper product according to the invention becomes less wavy due to swelling because the paper structure is stabilised by the resin. 15 - On account of the stiffness, it is easier to equip a press with impregnated papers than is the case with an unimpregnated base paper during a conventional pressing between two resin-impregnated papers. 20 A processing stage is eliminated compared with a subsequent impregnation which leads to significant cost advantages. - The laminate manufacturer can individually print each 25 quantity of decorative paper required without needing to havehis own impregnating equipment. For this purpose an ink jet printing equipment can be set up in the vicinity of a laminate press. Due to the decoupling of printing and impregnation, the general logistics for the product is 30 improved and the usage of material is optimized. TEST METHODS USED MI/ca 071858WO 17/06/2010 - 15 Testing the flow of an impregnate The flow is tested by determining the flow behaviour of the resin of the impregnating-resin impregnated decorative paper 5 (impregnate) . For this purpose five disks having a diameter of 4 cm are punched from an impregnate sample. These are pressed between an aluminium foil for 5 minutes (Wickert und Sahne precision press, 120 x 120 cm, pre-pressure: 46 bar/12 seconds, main pressure: 180 bar/12 seconds at 143 ± 2 0 C). 10 After the pressing process the disk laminate is cooled and weighed (initial weight). After removing the resin which has flowed out of the disk (the amount of resin located at the side of the blank), the laminate is weighed again (final weight). The difference between the initial and final weight, 15 related to the weight of the original disk laminate, gives the flow of the impregnate. Flow = Initial weight (g) - final weight (g) x 100 Initial weight (g) 20 Reactivity of the resin The reactivity is the minimum pressing time required at a specific temperature (e.g. 140 0 C) during which the surface is cured so much that a contaminant with the dye Rhodamine B can 25 easily be removed with water. Degree of cross-linking of the resin The degree of cross-linking is the quantity of impregnated resin which cannot be dissolved from the sample after dipping 30 for 35 minutes in DMF (dimethyl formamide) at room temperature. MI/ca 071858WO 17/06/2010 Residual moisture of an impregnate To this end circular samples (F 40 mm) are punched out and initially conditioned at 23 0 C, 50% room humidity, and weighed out. The weighed-out sample is dried for 5 minutes in a 5 drying cabinet at 160 0 C. The residual moisture is calculated as follows: Residual moisture (%) = Initial weight (g) - final weight (g) Initial weight (g) 10 Reactivity of the resin The test is used to determine the time curing behaviour of impregnated decorative papers. 15 To this end several circular samples having a diameter of 4 cm are punched out. These samples are then placed between the shiny sides of an aluminium film (thickness: 0.030 mm) and the package is placed in the middle of a heated press (Wickert und Sohne, pressing area 120 mm x 120 mm, pre 20 pressure setting 46 bar for 12 seconds, main pressure setting 180 bar from 12 seconds, temperature setting 140*C) . The press is started and the pressing program runs. The curing time defaults are 20 to 600 seconds in steps of 5 seconds (at the beginning) to 120 s (at the end). 25 After the pressing program has expired, the test specimens are immediately cooled between two sheets to stop the curing reaction. After cooling to 5 to 65 0 C, the test specimens are immersed 30 for three minutes in a 0.025% aqueous rhodamine B solution at a temperature of 95 0 C and then for 15 seconds in cold water. After drying with soft paper towels, the samples are glued onto a transparent film after increasing pressing times. The MI/ca 071858Wo 17/06/2010 - 17 assessment is made visually with respect to the reference sample. The reactivity value is achieved when the test specimens are only minimally coloured and no further change can be achieved due to longer pressing times. 5 Degree of cross-linking The test is used to determine the degree of curing of impregnates. 10 For this purpose test specimens having an area of 100 cm 2 are punched out and weighed (corresponds to sample weight "before extraction"). The test specimens are then dipped in N,N dimethyl formamide (DMF) (100 cm2 disks in 100 ml) . After an exposure time of 30 to 35 minutes at room temperature, the 15 test specimens are removed, placed on blotting paper and then dried in a drying cabinet at 1204C for 90 minutes. After cooling the test specimens are weighed (corresponds to sample weight "after extraction"). 20 Evaluation: Dissolved fractions (g) = initial weight (g) - final weight (g) 25 Dissolved fractions (%) = dissolved fractions (g)/initial weight (g) x 100 Cross-linked fractions (%) = final weight (g)/initial weight (g) x 100 30 Initial weight (g) sample weight "before extraction" (g) basis weight of base paper (g/m 2 ) x sample area (cmz)/10,000 MI/ca 071B58WO 17/06/2010 - 18 Final weight (g) sample weight "after extraction" (g) basis weight of base paper (g/m 2) x sample area (cm 2 ) /10, 000 MI/ca 071858WO 17/06/2010
Claims (9)
1. Decorative paper impregnate for decorative coating materials which contains an impregnated base paper and an ink receiving layer, characterised in that the base 5 paper contains an impregnating resin in a quantity of 40 to 250% by weight of the basis weight of the base paper, after drying the decorative paper impregnate has a residual moisture of at least 3.5% by weight and a flow of more than 0.4%, measured at a pressure of 180 bar and 10 a temperature of 143 ± 2 0 C.
2. The decorative paper impregnate according to claim 1, characterised in that the impregnating resin is contained in a quantity of 80 to 125% of the basis 15 weight in the base paper.
3. The decorative paper impregnate according to claim 1 and 2, characterised in that the impregnating resin is a melamine formaldehyde resin, a urea formaldehyde resin, 20 an acrylate resin or a mixture of these resins.
4. The decorative paper impregnate according to at least one of claims 1 to 3, characterised in that the impregnating resin is still reactive after drying the 25 decorative paper impregnate.
5. The decorative paper impregnate according to at least one of claims 1 to 4, characterised in that the ink receiving layer contains a pigment and a binder in a 30 quantitative ratio of 10:90 to 90:10. -2
6. The decorative paper impregnate according to claim 5, characterised in that the binder of the ink-receiving layer is a water-soluble and/or a water-dispersible polymer. 5
7. The decorative paper impregnate according to claim 5, characterised in that the pigment can be an aluminium oxide, aluminium hydroxide, boehmite and/or silica. 10 8. The decorative paper impregnate according to at least one of claims 1 to 7, characterized in that the application weight of the ink-receiving layer is 2 to 25 g/m 2 . 15 9. A method for producing a compressible decorative paper impregnate characterised in that (a) a decorative base paper fabricated with a basis weight of 30 to 200 g/m 2 is core-impregnated with an impregnating resin in a quantity of 40 to 250% by weight 20 of the basis weight of the base paper, (b) the core-impregnated paper is pre-dried, wherein the drying temperature is adjusted so that the paper has a moisture of 9 to 20% and the resin is only partially condensed and not completely polymerised and therefore 25 still reactive, (c) the pre-dried paper is coated with at least one ink receiving layer, (d) the core-impregnated decorative paper provided with at least one ink-receiving layer (decorative paper 30 impregnate) is dried to a residual moisture of 3.5 to
8.5%, wherein the resin is cross-linked at most to a degree of cross-linking of 30% and therefore still MI/ca 071858WO 17/06/2010 3 reactive and the dried decorative paper impregnate has a flow of more than 0.4% measured at a pressure of 180 bar and a temperature of 143 ± 2 0 C. 5 10. The method according to claim 9, characterised in that the impregnating resin is a melamine formaldehyde resin, a urea formaldehyde resin, an acrylate resin or a mixture of these resins. 10 11. The method according to claim 9 and 10, characterised in that the application weight of the ink-receiving layer is 2 to 25 g/m 2
12. Use of the decorative paper impregnate according to at 15 least one of claims 1 to 8 for producing layered pressed materials and laminates of all kinds. MI/ca 071858WO 17/06/2010
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU2013205626A AU2013205626A1 (en) | 2007-12-17 | 2013-04-14 | Compressible decorative paper impregnating agent which can be printed by the inkjet method |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07123355.5 | 2007-12-17 | ||
| AU2008337508A AU2008337508B2 (en) | 2007-12-17 | 2008-12-17 | Compressible decorative paper impregnating agent which can be printed by the inkjet method |
| AU2013205626A AU2013205626A1 (en) | 2007-12-17 | 2013-04-14 | Compressible decorative paper impregnating agent which can be printed by the inkjet method |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2008337508A Division AU2008337508B2 (en) | 2007-12-17 | 2008-12-17 | Compressible decorative paper impregnating agent which can be printed by the inkjet method |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AU2013205626A1 true AU2013205626A1 (en) | 2013-05-16 |
Family
ID=48538215
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2013205626A Abandoned AU2013205626A1 (en) | 2007-12-17 | 2013-04-14 | Compressible decorative paper impregnating agent which can be printed by the inkjet method |
Country Status (1)
| Country | Link |
|---|---|
| AU (1) | AU2013205626A1 (en) |
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2013
- 2013-04-14 AU AU2013205626A patent/AU2013205626A1/en not_active Abandoned
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Legal Events
| Date | Code | Title | Description |
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| MK17 | Application lapsed reg. 22.2b(2) - non-payment of filing fees |