EP1518024B2 - Prepreg - Google Patents
Prepreg Download PDFInfo
- Publication number
- EP1518024B2 EP1518024B2 EP04710840.2A EP04710840A EP1518024B2 EP 1518024 B2 EP1518024 B2 EP 1518024B2 EP 04710840 A EP04710840 A EP 04710840A EP 1518024 B2 EP1518024 B2 EP 1518024B2
- Authority
- EP
- European Patent Office
- Prior art keywords
- prepreg
- weight
- impregnation
- resin solution
- polymer dispersion
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 229920005989 resin Polymers 0.000 claims abstract description 38
- 239000011347 resin Substances 0.000 claims abstract description 38
- 238000004132 cross linking Methods 0.000 claims abstract description 21
- 238000005470 impregnation Methods 0.000 claims abstract description 21
- 238000000034 method Methods 0.000 claims abstract description 17
- 238000001035 drying Methods 0.000 claims abstract description 14
- 239000007787 solid Substances 0.000 claims abstract description 14
- 239000004815 dispersion polymer Substances 0.000 claims abstract description 13
- 229920000642 polymer Polymers 0.000 claims description 15
- 238000002156 mixing Methods 0.000 claims description 9
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 7
- 239000000463 material Substances 0.000 claims description 6
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 claims description 6
- 238000010526 radical polymerization reaction Methods 0.000 claims description 6
- 239000011248 coating agent Substances 0.000 claims description 5
- 238000000576 coating method Methods 0.000 claims description 5
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 2
- 125000005396 acrylic acid ester group Chemical group 0.000 claims description 2
- 239000003292 glue Substances 0.000 claims 1
- 239000000203 mixture Substances 0.000 abstract description 9
- 238000002360 preparation method Methods 0.000 abstract description 4
- 239000000123 paper Substances 0.000 description 43
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 25
- 239000003973 paint Substances 0.000 description 9
- 239000006185 dispersion Substances 0.000 description 8
- 238000012545 processing Methods 0.000 description 8
- 239000000654 additive Substances 0.000 description 4
- 238000009499 grossing Methods 0.000 description 3
- 238000007639 printing Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- NJVOHKFLBKQLIZ-UHFFFAOYSA-N (2-ethenylphenyl) prop-2-enoate Chemical compound C=CC(=O)OC1=CC=CC=C1C=C NJVOHKFLBKQLIZ-UHFFFAOYSA-N 0.000 description 2
- 229920005824 ACRODUR® 950 L Polymers 0.000 description 2
- 229920005789 ACRONAL® acrylic binder Polymers 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000011093 chipboard Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000005002 finish coating Substances 0.000 description 2
- 238000007731 hot pressing Methods 0.000 description 2
- 238000003475 lamination Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000000149 penetrating effect Effects 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 229920005823 ACRODUR® Polymers 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 244000166124 Eucalyptus globulus Species 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 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
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 235000010980 cellulose Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000000805 composite resin Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000011094 fiberboard Substances 0.000 description 1
- 238000009408 flooring Methods 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000007669 thermal treatment Methods 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H27/00—Special paper not otherwise provided for, e.g. made by multi-step processes
- D21H27/18—Paper- or board-based structures for surface covering
- D21H27/22—Structures being applied on the surface by special manufacturing processes, e.g. in presses
- D21H27/26—Structures being applied on the surface by special manufacturing processes, e.g. in presses characterised by the overlay sheet or the top layers of the structures
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/63—Inorganic compounds
- D21H17/70—Inorganic compounds forming new compounds in situ, e.g. within the pulp or paper, by chemical reaction with other substances added separately
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H25/00—After-treatment of paper not provided for in groups D21H17/00 - D21H23/00
- D21H25/04—Physical treatment, e.g. heating, irradiating
- D21H25/06—Physical treatment, e.g. heating, irradiating of impregnated or coated paper
Definitions
- the invention relates to prepregs, a process for their preparation and decorative coating materials obtainable therefrom.
- Decorative coating materials are preferably used for surface coating in furniture production and interior design, especially for laminate flooring.
- These decorative films are resin-impregnated and optionally subsequently surface-treated paper webs that are decorative printed or unprinted and in a no longer reactivated under pressure and heat condition.
- thermosetting decorative films with impregnated core offline process
- decorative films based on prepregs on-line process
- Decorative films based on prepregs are already more or less deeply soaked within the paper machine, immediately after sheet formation and drying, with a resin mixture, depending on the basis weight of the base paper. After drying and smoothing, usually also within the paper machine, the paper or the film must be crosslinked and thus be gap-resistant, so that during the subsequent processing steps of the finish coating and lamination on corresponding carrier no fiber separation occurs within the decorative film.
- the prepregs for further processing high coverage and surface quality, good printability in rotogravure, good paintability (high paint level), good flatness and bondability with chipboard and MDF boards (medium-density fiberboard) required.
- the thermally crosslinkable impregnating resins commonly used for the preparation of prepregs are water-dilutable, formaldehyde-containing resin solutions based on urea, melamine or phenolic resins. Since their sole use leads to relatively brittle products, these resin solutions are generally used in combination with water-dilutable, thermally crosslinkable polymer dispersions based on acrylic acid, acrylic acid ester, styrene, butadiene, vinyl acetate or acrylonitrile.
- the resin absorption can be between 5 and 35% by weight, with the proportion of resin solutions generally penetrating deeper into the base paper than the proportion of polymer dispersions.
- the latter are more or less rich on the top and bottom of the paper and ensure good smoothability and thus printability and Oberfilumbleendimi and thus paintability (paint level) of the papers.
- the resin solutions are intended to ensure the good gap strength and flatness of the prepreg by crosslinking the fiber-resin composite during further processing.
- the penetration depth of polymer dispersions can be increased by various additives, for example by water-soluble polymers based on polyvinyl alcohols, gelatin, starches, cellulose derivatives, alginates and mixtures thereof (EP 0739 435 B1 ), Maleic acid copolymers (EP 0 223 922 A1 ) or a copolymer of (meth) acrylamide and (meth) acrylic acid ( DE 197 28 250 A1 and DE 197 584 79 A1 ).
- the first at a heat treatment of the prepreg over a period of about 40 seconds at about 132 ° C according to DE 101 34 302 C1 largely crosslinked (degree of crosslinking of at most 85%), these disadvantages are avoided.
- the resin solution used for this purpose, its production and possible uses, inter alia for the impregnation of papers for decorative applications, are in the DE 197 35 959 A1 described.
- a disadvantage is that such until hot compression on the carrier material (eg chipboard) as the last further processing step completely unvemetztes prepreg according to DE 101 34 302 C2 until then has no better or even worse internal strengths than known formaldehyde-free or -contaminated prepregs.
- the invention is therefore an object of the invention to provide teilvemetzten prepregs that largely avoid the disadvantages mentioned at the end of the paper machine and as far as possible by high surface quality, good printability and higher splitting strength than known formaldehyde-free or prepregs, good paintability (high paint level) , good flatness and bondability with conventional adhesives Characterized in the subsequent processing stages and thus are almost equivalent in properties off-line impregnated papers.
- the prepreg according to the invention is obtainable by impregnating a base paper with a Impregnating combination containing a thermally curable, formaldehyde-free resin solutions and a thermally crosslinkable polymer dispersion.
- the impregnated base paper is dried and smoothed. The smoothing is expediently carried out within the paper machine used to produce the prepreg.
- the degree of crosslinking of the prepreg is at least 10% and at most 85%.
- the impregnated base paper has a residual moisture of 2 to 3 wt .-%.
- the degree of crosslinking is analogous to that in the DE 101 34 302 C1 test method described by punching an area of 100 cm 2 in a pre-impregnate, weighed and kept in water at a temperature of 60 ° C for 15 minutes, rinsed, dried in an oven at 130 ° C and weighed again. From the weight difference and the known order of the impregnating resin or the impregnating combination (eg 12 g / m 2 dry with a 60 g / m 2 pre-impregnate), the soluble fraction of the polymer or polymers can be determined. The degree of crosslinking in% is then 100 - soluble fraction in%.
- the invention also provides a process for producing thermally partially crosslinked, formaldehyde-free prepregs within the paper machine and their use as decorative coating materials.
- prepregs are understood to mean partially impregnated papers in the formaldehyde-free resin solutions in combination with polymer dispersions.
- the proportion of the impregnating components is from 5 to 35% by weight, preferably from 10 to 30% by weight, based on the weight of the raw paper.
- the residual moisture content of the prepreg is between 1.5 and 3% by weight. At residual moisture contents of more than 3.5% by weight, the prepreg can adhere to machine parts, for example to the calender rolls of the paper machine.
- a resin for impregnating the base paper, a resin can be used which contains the aforementioned components B) and C), but not the component A).
- Such resins are in the DE 197 35 959 A1 disclosed.
- the inventive water-dilutable impregnating mixture from o.g. Formaldehyde-free resin solutions A) + B) + C) or B) + C) and commonly used polymer dispersions is applied to at least one side of the paper web, then dried to a residual moisture content of 2 to 3 wt .-% and then smoothed.
- the impregnated base paper is thereby partially crosslinked, the degree of crosslinking depending on the mixing ratio of the impregnating combination between at least 10% and max. 85%
- this partially crosslinked prepreg is sufficiently flexible. It is particularly advantageous for the quality of the prepreg if the residual moisture is already set in the paper machine ("on-line"). Under a paper machine is understood in accordance with the general use of the word, the plant for papermaking, starting from the screening of the pulp suspension to the rolling up of the base paper.
- the mixing ratio between formaldehyde-free resin solution (I) and polymer dispersion (II) is (solid: solid), 45:55 to 30:70. Mixture ratios of 35:65 to 30:70 are particularly preferred, since prepregs which have been produced with impregnation combinations having these mixing ratios are particularly easy to print and are sufficiently flexible.
- the concentration of the impregnating mixture according to the invention, which contains further additives if required, can be up to 50% by weight.
- the impregnating combination according to the invention can be applied online to the paper web in an amount of between 5 and 35% by weight, preferably between 10 and 30% by weight, based on the basis weight of the base paper.
- application devices all commonly used within the paper machine units can be used, preferably roller application devices, such as size press or film press.
- prepregs according to the invention already have better properties than previously known formaldehyde-containing and formaldehyde-free prepregs with regard to printability and surface strength (Tesafestmaschine) immediately after the paper machine. At the same time they retain a high surface density (high paint level) and dimensional stability / flatness, the formaldehyde-free uncrosslinked prepregs according to DE 101 34 302 C1 , so impregnated with the above-mentioned formaldehyde-free resin solutions according to DE 197 35 959 A1 do not own after the paper machine. In the case of the last-mentioned prepreg, partial crosslinking takes place only at the end of the entire process chain of further processing, ie hot-pressing.
- the prepreg according to the invention is thus significantly more universally applicable in the further processing steps and is not subject to any technological limitations with respect to various process parameters, such as speed, temperature and pressure.
- the prepregs according to the invention can be prepared so that they have high flexibility, dimensional stability and good barrier properties against water and solvents and can be used in particular as a base material for high-quality specialty papers, such as printing and advertising media, decorative wall materials, abrasive papers, adhesive tapes or floor coverings.
- the raw papers to be impregnated according to the invention are those which are described, inter alia, in the patents EP 0223 922 A1 .
- EP 0870 872 A1 and DE 101 34 302 A1 are described.
- the impregnation, drying and smoothing methods used in the documents cited and in the trade journal " Kliblatt für Textilfabrikation "No. 6 (2000), pp. 350 to 355 described in detail and known prior art.
- a raw paper of 20% pine sulfate pulp and 80% eucalyptus pulp was produced.
- the freeness was 30 ° SR (Schopper-Riegler).
- the additives used were 25% titanium dioxide and 4% formaldehyde-free wet strength agent on dry pulp.
- This raw paper without engine sizing and with a basis weight of 48 g / m 2 was impregnated on both sides in a laboratory size press with a formaldehyde-free resin solution of about 30% solids content of modified polyacrylic acid and a polyhydric alcohol (Acrodur 950 L Fa. BASF) and then at dried at different temperatures within about 18 seconds to a residual moisture content of about 2%.
- the amount applied after drying was 10 g / m 2 .
- Table 1 shows the degrees of crosslinking of the prepregs dried at different temperatures. This is followed by partial cross-linking of the prepregs up to about 30%, with drying conditions customary in the paper machine (up to 110 ° C., drying time about 300 seconds).
- the base paper from Example 1 was impregnated by means of a laboratory size press with the impregnating mixture according to the invention from a formaldehyde-free resin solution (Acrodur 950 L) and a styrene-acrylate dispersion (Acronal 305 D from BASF) in a ratio of 35:65 (solid: solid) and dried at temperatures of about 110 ° C to a residual moisture content of about 2% within about 18 seconds.
- a formaldehyde-free resin solution Acrodur 950 L
- a styrene-acrylate dispersion Acronal 305 D from BASF
- the order amount was about 12 g / m 2 .
- the degree of crosslinking of the prepreg according to the invention was about 70%.
- the addition of polymer dispersion to the resin solution significantly increases the degree of crosslinking.
- the base paper from Example 1 was produced by means of a laboratory size press with a commonly used impregnation mixture for classic prepregs of formaldehyde-free styrene-acrylate dispersion (Acronal 305) and formaldehyde-containing resin solution (Urecoll TS) in the ratios 70:30 (A) and 90:10 (B) ( solid calculated) and then dried analogously to Example 2.
- the order amount was in each case about 13 g / m 2 .
- the degree of crosslinking of the classical prepreg was 76% (A) or 84% (B) and is thus significantly higher than that of prepregs according to the invention with proportions of formaldehyde-free resin solutions according to Examples 1 and 2
- the formaldehyde-free prepreg according to the invention (Example 2) has a significantly better nip strength and printability.
- the paint level remains at a high level of quality, while the flatness gets a little worse.
- the prepreg of the invention is characterized by improved surface impermeability and thus significantly higher paint level, lower color penetration (pinhole test) and better printability and higher flatness.
- the significantly better properties of the thermally partially crosslinked prepreg according to the invention are caused by the combination of resin solution and polymer dispersion in a certain range of the mixing ratios and the resulting higher levels of crosslinking than with the resin solution alone.
- Example 3 Example 3 (B) example 1 Example 2 area based size, g / m 2 about 60 about 60 about 60 about 60 Order quantity, g / m 2 about 13 about 13 about 10 about 12 Degree of crosslinking,% (110 ° C, ⁇ 20 seconds) about 76 about 84 about 30 about 70 Water absorption, g / m 2 17.0 20.0 37.8 23.0 Porosity after Bendtsen, ml / min 37.1 36.0 250 14.5 Smoothness to Bekk, s 296 310 285 320 Flatness, s 14 5 6 10 Splitting strength / Tesatest 3 5 1 1 Paint level / shine, % 84.6 82.1 21.0 81.8 Pinhole Test 1 1 4 2 Printability (aqueous intaglio printing) 3 3 4 1 Formaldehyde emission, mg
Landscapes
- Reinforced Plastic Materials (AREA)
- Paper (AREA)
- Glass Compositions (AREA)
- Laminated Bodies (AREA)
Abstract
Description
Die Erfindung betrifft Vorimprägnate, ein Verfahren zu deren Herstellung sowie daraus erhältliche dekorative Beschichtungswerkstoffe.The invention relates to prepregs, a process for their preparation and decorative coating materials obtainable therefrom.
Dekorative Beschichtungswerkstoffe, sogenannte Dekorpapiere oder Dekorfolien, werden vorzugsweise zur Oberflächenbeschichtung bei der Möbelherstellung und im Innenausbau, insbesondere für Laminatböden, eingesetzt. Diese Dekorfolien sind kunstharzgetränkte und gegebenenfalls nachträglich oberflächenbehandelte Papierbahnen, die dekorativ bedruckt oder unbedruckt und in einem unter Druck und Wärme nicht mehr reaktivierbaren Zustand sind. Je nach Art des Tränkverfahrens wird zwischen duroplastischen Dekorfolien mit durchimprägniertem Kem (offline-Verfahren) und Dekorfolien auf der Basis von Vorimprägnaten (online-Verfahren) unterschieden, auf denen anschließend eine Finish-Beschichtung vorgenommen werden kann. Somit entsteht eine Dekorfolie, die eine fertige Oberfläche besitzt.Decorative coating materials, so-called decor papers or decorative films, are preferably used for surface coating in furniture production and interior design, especially for laminate flooring. These decorative films are resin-impregnated and optionally subsequently surface-treated paper webs that are decorative printed or unprinted and in a no longer reactivated under pressure and heat condition. Depending on the type of impregnation process, a distinction is made between thermosetting decorative films with impregnated core (offline process) and decorative films based on prepregs (on-line process), on which subsequently a finish coating can be carried out. This creates a decorative film that has a finished surface.
Dekorfolien auf der Basis von Vorimprägnaten werden bereits innerhalb der Papiermaschine, unmittelbar nach der Blattbildung und Trocknung, mit einem Harzgemisch in Abhängigkeit von der flächenbezogenen Masse des Basispapiers mehr oder weniger tief getränkt. Nach der Trocknung und Glättung, meist ebenfalls innerhalb der Papiermaschine, muss das Papier oder die Folie vernetzt und damit spaltfest sein, damit bei den nachfolgenden Verarbeitungsschritten der Finish-Beschichtung und Kaschierung auf entsprechende Träger keine Fasertrennung innerhalb der Dekorfolie eintritt. Außerdem wird von den Vorimprägnaten für die weitere Verarbeitung eine hohe Deckkraft und Oberflächengüte, gute Bedruckbarkeit im Rotationstiefdruck, gute Lackierbarkeit (hoher Lackstand), gute Planlage und Verklebbarkeit mit Span- und MDF Platten (mitteldichte Faserplatten) verlangt.Decorative films based on prepregs are already more or less deeply soaked within the paper machine, immediately after sheet formation and drying, with a resin mixture, depending on the basis weight of the base paper. After drying and smoothing, usually also within the paper machine, the paper or the film must be crosslinked and thus be gap-resistant, so that during the subsequent processing steps of the finish coating and lamination on corresponding carrier no fiber separation occurs within the decorative film. In addition, the prepregs for further processing high coverage and surface quality, good printability in rotogravure, good paintability (high paint level), good flatness and bondability with chipboard and MDF boards (medium-density fiberboard) required.
Die für die Herstellung von Vorimprägnaten üblicherweise eingesetzten thermisch vernetzbaren Imprägnierharze sind wasserverdünnbare, formaldehydhaltige Harzlösungen auf der Basis von Harnstoff-, Melamin- oder Phenolharzen. Da ihre alleinige Verwendung zu relativ spröden Produkten führt, werden diese Harziösungen im allgemeinen in Kombination mit wasserverdünnbaren, thermisch vernetzbaren Polymerdispersionen auf der Basis von Acrylsäure, Acrylsäureester, Styrol, Butadien, Vinylacetat oder Acrylnitril eingesetzt.The thermally crosslinkable impregnating resins commonly used for the preparation of prepregs are water-dilutable, formaldehyde-containing resin solutions based on urea, melamine or phenolic resins. Since their sole use leads to relatively brittle products, these resin solutions are generally used in combination with water-dilutable, thermally crosslinkable polymer dispersions based on acrylic acid, acrylic acid ester, styrene, butadiene, vinyl acetate or acrylonitrile.
Bei Vorimprägnaten kann die Harzaufnahme zwischen 5 und 35 Gew.-% betragen, wobei im allgemeinen der Anteil an Harzlösungen tiefer in das Rohpapier penetriert als der Anteil an Polymerdispersionen. Letztere reichem sich mehr oder weniger an der Ober- und Unterseite des Papiers an und gewährleisten eine gute Glättbarkeit und damit Bedruckbarkeit sowie Oberfilächendichtigkeit und damit Lackierbarkeit (Lackstand) der Papiere. Die Harzlösungen dagegen sollen die gute Spaltfestigkeit und Planlage des Vorimprägnats durch Vernetzung des Faser-Harz-Verbundes während der weiteren Verarbeitungsprozesse gewährleisten.In the case of prepregs, the resin absorption can be between 5 and 35% by weight, with the proportion of resin solutions generally penetrating deeper into the base paper than the proportion of polymer dispersions. The latter are more or less rich on the top and bottom of the paper and ensure good smoothability and thus printability and Oberfilächendichtigkeit and thus paintability (paint level) of the papers. In contrast, the resin solutions are intended to ensure the good gap strength and flatness of the prepreg by crosslinking the fiber-resin composite during further processing.
Die Penetrationstiefe von Polymerdispersionen kann durch verschiedene Additive erhöht werden, wie z.B. durch wasserlösliche Polymere auf der Basis von Polyvinylalkoholen, Gelatine, Stärken, Cellulosederivaten, Alginaten und deren Mischungen (
Teilweise wird bei der Herstellung der Vorimprägnate unter Verwendung o.g. Additive gänzlich auf den Einsatz von klassischen formaldehydhaltigen-Harzlösungen verzichtet. Diese dann formaldehydfreien Vorimprägnate sind jedoch in ihrer Spaltfestigkeit, Planlage und Bedruckbarkeit begrenzt.Partially used in the preparation of the prepregs using o.g. Additives completely dispensed with the use of classical formaldehyde-containing resin solutions. These then formaldehyde-free prepregs, however, are limited in their gap strength, flatness and printability.
Durch die Verwendung einer thermisch härtbaren, formaldehydfreien Harzlösung, die erst bei einer Wärmebehandlung des Vorimprägnats Ober einen Zeitraum von etwa 40 Sekunden bei etwa 132 °C gemäß
Der Erfindung liegt daher die Aufgabe zugrunde, teilvemetzte Vorimprägnate bereitzustellen, die bereits am Ende der Papiermaschine die genannten Nachteile weitgehend vermeiden und sich nach Möglichkeit durch hohe Oberflächengüte, gute Bedruckbarkeit und höhere Spaltfestigkeit als bekannte formaldehydfreie oder -haltige Vorimprägnate, gute Lackierbarkeit (hoher Lackstand), gute Planlage und Verklebbarkeit mit üblichen Klebstoffen In den nachfolgenden Verarbeitungsstufen auszeichnen und damit off line imprägnierten Papieren in ihren Eigenschaften nahezu gleichwertig sind.The invention is therefore an object of the invention to provide teilvemetzten prepregs that largely avoid the disadvantages mentioned at the end of the paper machine and as far as possible by high surface quality, good printability and higher splitting strength than known formaldehyde-free or prepregs, good paintability (high paint level) , good flatness and bondability with conventional adhesives Characterized in the subsequent processing stages and thus are almost equivalent in properties off-line impregnated papers.
Gelöst wird diese Aufgabe durch ein formaldehydfreies Vorimprägnat mit den Merkmalen gemäß Patentanspruch 1. Weitere vorteilhafte Ausführungsformen ergeben sich aus den Unteransprüchen.This object is achieved by a formaldehyde-free prepreg having the features of claim 1. Further advantageous embodiments will become apparent from the dependent claims.
In verfahrensmäßiger Hinsicht wird die Aufgabe gelöst durch ein Verfahren gemäß Patentanspruch 8, wobei vorteilhafte weitere Ausführungsformen in den entsprechenden Unteransprüchen angegeben sind.In procedural terms, the object is achieved by a method according to claim 8, wherein advantageous further embodiments are specified in the corresponding subclaims.
Das erfindungsgemäße Vorimprägnat ist erhältlich durch Imprägnieren eines Rohpapiers mit einer Imprägnier-Kombination, die eine thermisch härtbare, formaldehydfreie Harzlösungen und eine thermisch vemetzbare Polymerdispersion enthält. Das imprägnierte Rohpapier wird getrocknet und geglättet. Das Glätten erfolgt zweckmäßigerweise innerhalb der zur Herstellung des Vorimprägnats verwendeten Papiermaschine. Der Vernetzungsgrad des Vorimprägnats beträgt mindestens 10 % und höchstens 85 %. Das imprägnierte Rohpapier hat eine Restfeuchte von 2 bis 3 Gew.-%.The prepreg according to the invention is obtainable by impregnating a base paper with a Impregnating combination containing a thermally curable, formaldehyde-free resin solutions and a thermally crosslinkable polymer dispersion. The impregnated base paper is dried and smoothed. The smoothing is expediently carried out within the paper machine used to produce the prepreg. The degree of crosslinking of the prepreg is at least 10% and at most 85%. The impregnated base paper has a residual moisture of 2 to 3 wt .-%.
Der Vernetzungsgrad wird analog der in der
Gegenstand der Erfindung ist auch ein Verfahren zur Herstellung thermisch teilvemetzter, formaldehydfreier Vorimprägnate innerhalb der Papiermaschine und deren Verwendung als dekorative Beschichtungswerkstoffe. Unter Vorimprägnaten werden erfindungsgemäß mit formaldehydfreien Harzlösungen in Kombination mit Polymerdispersionen teilimprägnierte Papiere verstanden. Der Anteil der Imprägnierkomponenten beträgt 5 bis 35 Gew.-%, vorzugsweise 10 bis 30 Gew.-%, bezogen auf das Rohpapiergewicht.The invention also provides a process for producing thermally partially crosslinked, formaldehyde-free prepregs within the paper machine and their use as decorative coating materials. According to the invention, prepregs are understood to mean partially impregnated papers in the formaldehyde-free resin solutions in combination with polymer dispersions. The proportion of the impregnating components is from 5 to 35% by weight, preferably from 10 to 30% by weight, based on the weight of the raw paper.
Die Restfeuchte des Vorimprägnats beträgt zwischen 1,5 bis 3 Gew.-%. Bei Restfeuchten von mehr als 3,5 Gew.-% kann das Vorimprägnat an Maschinenteilen anhaften, beispielsweise an den Glättwerkswalzen der Papiermaschine.The residual moisture content of the prepreg is between 1.5 and 3% by weight. At residual moisture contents of more than 3.5% by weight, the prepreg can adhere to machine parts, for example to the calender rolls of the paper machine.
Zum Imprägnieren geeignete formaldehydfreie Harzlösungen sind die in der
- A) mindestens ein durch radikalische Polymerisation erhältliches Polymerisat, das weniger als 5 Gew.-% einer α, β-ethylenisch ungesättigten Mono- oder Dicarbonsäure einpolymerisiert enthält,
- B) mindestens ein durch radikalische Polymerisation erhältliches Polymerisat, das mehr als 15 Gew.-% einer α, β-ethylenisch ungesättigten Mono- oder Dicarbonsäure einpolymerisiert enthält, und
- C) mindestens ein Alkanolamin mit mindestens zwei Hydroxylgruppen.
- A) at least one polymer obtainable by free-radical polymerization and containing less than 5% by weight of an α, β-ethylenically unsaturated mono- or dicarboxylic acid in copolymerized form,
- B) at least one polymer obtainable by free-radical polymerization which contains more than 15% by weight of an α, β-ethylenically unsaturated mono- or dicarboxylic acid in copolymerized form, and
- C) at least one alkanolamine having at least two hydroxyl groups.
Gemäß einer besonders bevorzugten Ausführungsform kann zum Imprägnieren des Rohpapiers ein Harz eingesetzt werden, das die zuvor genannten Komponenten B) und C), nicht aber die Komponente A) enthält. Solche Harze sind in der
Die erfindungsgemäße wasserverdünnbare Imprägniermischung aus o.g. formaldehydfreien Harzlösungen A) + B) + C) oder B) + C) und üblicherweise verwendeten Polymerdispersionen wird auf mindestens eine Seite der Papierbahn aufgebracht, anschließend bis zu einer Restfeuchte von 2 bis 3 Gew.-% getrocknet und danach geglättet. Das imprägnierte Rohpapier ist dadurch teilvernetzt, wobei der Vernetzungsgrad je nach Mischungsverhältnis der Imprägnier-Kombination zwischen mindestens 10 % und max. 85 % beträgt, In den nachfolgenden Verarbeitungsschritten, wie Bedrucken, Lackieren und KaschierenNerkleben ist dieses nur teilvemetzte Vorimprägnat ausreichend flexibel. Besonders vorteilhaft für die Qualität des Vorimprägnats ist es, wenn die Restfeuchte bereits in der Papiermaschine ("on-line") eingestellt wird. Unter eine Papiermaschine wird dabei in Übereinstimmung mit dem allgemeinen Gebrauch des Wortes die Anlage zur Papierherstellung, angefangen vom Sieben der Faserstoffsuspension bis zum Aufrollen des Rohpapiers verstanden.The inventive water-dilutable impregnating mixture from o.g. Formaldehyde-free resin solutions A) + B) + C) or B) + C) and commonly used polymer dispersions is applied to at least one side of the paper web, then dried to a residual moisture content of 2 to 3 wt .-% and then smoothed. The impregnated base paper is thereby partially crosslinked, the degree of crosslinking depending on the mixing ratio of the impregnating combination between at least 10% and max. 85% In the subsequent processing steps, such as printing, painting and laminating, this partially crosslinked prepreg is sufficiently flexible. It is particularly advantageous for the quality of the prepreg if the residual moisture is already set in the paper machine ("on-line"). Under a paper machine is understood in accordance with the general use of the word, the plant for papermaking, starting from the screening of the pulp suspension to the rolling up of the base paper.
Das Mischungsverhältnis zwischen formaldehydfreier Harzlösung (I) und Polymerdispersion (II) Beträgt (fest:fest), 45:55 bis 30:70. Besonders bevorzugt sind Mischungsverhältnisse von 35:65 bis 30:70, da Vorimprägnate, die mit Imprägnier-Kombinationen mit diesen Mischungsverhältnissen hergestellt wurden, besonders gut bedruckbar und ausreichend flexibel sind.The mixing ratio between formaldehyde-free resin solution (I) and polymer dispersion (II) is (solid: solid), 45:55 to 30:70. Mixture ratios of 35:65 to 30:70 are particularly preferred, since prepregs which have been produced with impregnation combinations having these mixing ratios are particularly easy to print and are sufficiently flexible.
Die Konzentration der erfindungsgemäßen Imprägniermischung, die bei Bedarf weitere Additive enthält, kann bis zu 50 Gew.-% betragen. Die erfindungsgemäße Imprägnier-Kombination kann online auf die Papierbahn in einer Menge zwischen 5 und 35 Gew.-%, vorzugsweise zwischen 10 und 30 Gew.-%, bezogen auf das Flächengewicht des Rohpapiers, aufgetragen werden. Als Auftragsvorrichtungen können alle üblicherweise innerhalb der Papiermaschine angewendeten Aggregate eingesetzt werden, vorzugsweise Walzenauftragsvorrichtungen, wie Leimpresse oder Filmpresse.The concentration of the impregnating mixture according to the invention, which contains further additives if required, can be up to 50% by weight. The impregnating combination according to the invention can be applied online to the paper web in an amount of between 5 and 35% by weight, preferably between 10 and 30% by weight, based on the basis weight of the base paper. As application devices, all commonly used within the paper machine units can be used, preferably roller application devices, such as size press or film press.
Überraschend wurde festgestellt, dass die erfindungsgemäßen Vorimprägnate bereits unmittelbar nach der Papiermaschine bessere Eigenschaften als bisher bekannte formaldehydhaltige und formaldehydfreie Vorimprägnate bezüglich Bedruckbarkeit und Oberflächenfestigkeit (Tesafestigkeit) aufweisen. Gleichzeitig behalten sie aber eine hohe Oberflächendichtigkeit (hoher Lackstand) sowie Dimensionsstabilität/Planlage, die formaldehydfreie unvernetzte Vorimprägnate gemäß
Erreicht werden diese hervorragenden Eigenschaften des erfindungsgemäßen Vorimprägnats durch die Kombination von Harzlösungen und Polymerdispersionen in einem bestimmten Abmischungsverhältnis, bei dem sich ein Optimum zwischen penetrierenden und filmbildenden Eigenschaften der Einzelkomponenten beim Imprägnieren des Rohpapiers einstellt und das bereits innerhalb der Papiermaschine, vermutlich durch Synergieeffekte und Temperatureinfluß, weitgehend seinen endgültigen Zustand erreicht hat.These outstanding properties of the prepreg according to the invention are achieved by the combination of resin solutions and polymer dispersions in a certain mixing ratio, in which an optimum between penetrating and film-forming properties of the individual components in the impregnation of the base paper and the already within the paper machine, probably by synergy effects and temperature influence, has largely reached its final state.
Das erfindungsgemäße Vorimprägnat ist dadurch bedeutend universeller in den Weiterverarbeitungsschritten einsetzbar und unterliegt keinen technologischen Einschränkungen bezüglich verschiedener Prozessparameter, wie Geschwindigkeit, Temperatur und Druck. Insbesondere können die erfindungsgemäßen Vorimprägnate so hergestellt werden, dass sie eine hoher Flexibilität, Dimensionsstabilität und gute Sperreigenschaften gegen Wasser und Lösungsmittel besitzen und insbesondere als Basismaterial für hochwertige Spezialpapiere, wie Druck- und Werbeträger, dekorative Wandmaterialien, Schleifpapiere, Klebebänder oder Fußbodenbeläge einsetzbar sind.The prepreg according to the invention is thus significantly more universally applicable in the further processing steps and is not subject to any technological limitations with respect to various process parameters, such as speed, temperature and pressure. In particular, the prepregs according to the invention can be prepared so that they have high flexibility, dimensional stability and good barrier properties against water and solvents and can be used in particular as a base material for high-quality specialty papers, such as printing and advertising media, decorative wall materials, abrasive papers, adhesive tapes or floor coverings.
Besonders gute Vorimprägnat-Qualitäten konnten erreicht werden, wenn der Vernetzungsgrad des Vorimprägnats mehr als 50 %, vorzugsweise 70 % und mehr beträgt.Particularly good pre-impregnate qualities could be achieved if the degree of crosslinking of the prepreg is more than 50%, preferably 70% or more.
Die erfindungsgemäß zu imprägnierenden Rohpapiere sind solche, die u.a. in den Patentschriften
Die folgenden Beispiele erläutern die Erfindung. Alle Mengenangaben beziehen sich auf den Feststoff oder Feststoffgehalt, sofern nichts anderes angegeben ist.The following examples illustrate the invention. All quantities are based on the solids or solids content, unless stated otherwise.
Erfindungsgemäß wurde ein Rohpapier aus 20 % Kiefernsulfat-Zellstoff und 80 % EukalyptusZellstoff hergestellt. Der Mahlgrad betrug 30 °SR (Schopper-Riegler). Als Zusätze wurden-auf atro Zellstoff 25 % Titandioxid und 4 % formaldehydfreies Nassfestmittel eingesetzt. Dieses Rohpapier ohne Masseleimung und mit einer flächenbezogenen Masse von 48 g/m2 wurde in einer Laborleimpresse mit einer formaldehydfreien Harzlösung von ca. 30 % Feststoffgehalt aus modifizierter Polyacrylsäure und einem mehrwertigen Alkohol (Acrodur 950 L der Fa. BASF) beidseitig imprägniert und anschließend bei unterschiedlichen Temperaturen innerhalb von ca. 18 Sekunden bis zu einer Restfeuchte von ca. 2 % getrocknet.According to the invention, a raw paper of 20% pine sulfate pulp and 80% eucalyptus pulp was produced. The freeness was 30 ° SR (Schopper-Riegler). The additives used were 25% titanium dioxide and 4% formaldehyde-free wet strength agent on dry pulp. This raw paper without engine sizing and with a basis weight of 48 g / m 2 was impregnated on both sides in a laboratory size press with a formaldehyde-free resin solution of about 30% solids content of modified polyacrylic acid and a polyhydric alcohol (Acrodur 950 L Fa. BASF) and then at dried at different temperatures within about 18 seconds to a residual moisture content of about 2%.
Die Auftragsmenge nach der Trocknung betrug 10 g/m2.The amount applied after drying was 10 g / m 2 .
In der Tabelle 1 sind die Vemetzungsgrade der bei unterschiedlichen Temperaturen getrockneten Vorimprägnate zusammengestellt. Danach erfolgt bei in der Papiermaschine üblichen Trocknungsbedingungen (bis 110 °C, Trocknungsdauer ca. 14 Sekunden bei 300 m/min) eine Teilvernetzung der Vorimprägnate bis zu etwa 30 %.Table 1 shows the degrees of crosslinking of the prepregs dried at different temperatures. This is followed by partial cross-linking of the prepregs up to about 30%, with drying conditions customary in the paper machine (up to 110 ° C., drying time about 300 seconds).
Das Rohpapier aus Beispiel 1 wurde mittels einer Laborleimpresse mit der erfindungsgemäßen Imprägniermischung aus einer formaldehydfreien Harzlösung (Acrodur 950 L) und einer Styrol-Acrylat-Dispersion (Acronal 305 D der Fa. BASF) im Verhältnis 35:65 (fest:fest) imprägniert und bei Temperaturen von etwa 110 °C bis zu einer Restfeuchte von ca. 2 % innerhalb von ca. 18 Sekunden getrocknet.The base paper from Example 1 was impregnated by means of a laboratory size press with the impregnating mixture according to the invention from a formaldehyde-free resin solution (Acrodur 950 L) and a styrene-acrylate dispersion (Acronal 305 D from BASF) in a ratio of 35:65 (solid: solid) and dried at temperatures of about 110 ° C to a residual moisture content of about 2% within about 18 seconds.
Die Auftragsmenge betrug etwa 12 g/m2. Der Vernetzungsgrad des erfindungsgemäßen Vorimprägnats betrug ca. 70 %. Demnach erhöht der Zusatz an Polymerdispersion zur Harzlösung den Vernetzungsgrad signifikant.The order amount was about 12 g / m 2 . The degree of crosslinking of the prepreg according to the invention was about 70%. Thus, the addition of polymer dispersion to the resin solution significantly increases the degree of crosslinking.
Das Rohpapier aus Beispiel 1 wurde mittels Laborleimpresse mit einer üblicherweise eingesetzten Imprägniermischung für klassische Vorimprägnate aus formaldehydfreier Styrol-Acrylat-Dispersion (Acronal 305) und formaldehydhaltiger Harzlösung (Urecoll TS) im Verhältnis 70:30 (A) und 90:10 (B) (fest gerechnet) imprägniert und danach analog Beispiel 2 getrocknet. Die Auftragsmenge betrug jeweils ca. 13 g/m2.The base paper from Example 1 was produced by means of a laboratory size press with a commonly used impregnation mixture for classic prepregs of formaldehyde-free styrene-acrylate dispersion (Acronal 305) and formaldehyde-containing resin solution (Urecoll TS) in the ratios 70:30 (A) and 90:10 (B) ( solid calculated) and then dried analogously to Example 2. The order amount was in each case about 13 g / m 2 .
Der Vernetzungsgrad des klassischen Vorimprägnats betrug 76 % (A) bzw. 84 % (B) und liegt damit signifikant höher als der von erfindungsgemäßen Vorimprägnaten mit Anteilen an formaldehydfreien Harzlösungen gemäß Beispiel 1 und 2The degree of crosslinking of the classical prepreg was 76% (A) or 84% (B) and is thus significantly higher than that of prepregs according to the invention with proportions of formaldehyde-free resin solutions according to Examples 1 and 2
Die gemäß Beispiel 1 bis 3 hergestellten Vorimprägnate wurden unter konstanten Bedingungen in einem Laborkalander geglättet. Die erreichten Papiereigenschaften sind in der Tabelle 2 zusammengestellt.The Vorimprägnate prepared according to Example 1 to 3 were under constant conditions in a Smoothed laboratory calender. The paper properties achieved are summarized in Table 2.
Im Vergleich zu üblicherweise eingesetzten formaldehydhaltigen bzw. formaldehydarmen Vorimprägnaten (Vergleichsbeispiele 3 A und 3 B) weist das erfindungsgemäße formaldehydfreie Vorimprägnat (Beispiel 2) eine bedeutend bessere Spaltfestigkeit und Bedruckbarkeit auf. Der Lackstand bleibt auf hohem Qualitätsniveau, während die Planlage etwas schlechter wird.In comparison to conventionally used formaldehyde-containing or low-formaldehyde prepregs (Comparative Examples 3 A and 3 B), the formaldehyde-free prepreg according to the invention (Example 2) has a significantly better nip strength and printability. The paint level remains at a high level of quality, while the flatness gets a little worse.
Im Gegensatz zum formaldehydfreien Vorimprägnat gemäß Beispiel 1 zeichnet sich das erfindungsgemäße Vorimprägnat (Beispiel 2) durch eine verbesserte Oberflächendichtigkeit und damit bedeutend höheren Lackstand, geringeren Farbdurchschlag (Pinhole-Test) und bessere Bedruckbarkeit sowie höhere Planlage aus.In contrast to the formaldehyde-free prepreg according to Example 1, the prepreg of the invention (Example 2) is characterized by improved surface impermeability and thus significantly higher paint level, lower color penetration (pinhole test) and better printability and higher flatness.
Die signifikant besseren Eigenschaften des erfindungsgemäßen thermisch teilvemetzten Vorimprägnats sind verursacht durch die Kombination von Harzlösung und Polymerdispersion in einem bestimmten Bereich der Mischungsverhältnisse sowie der sich dadurch einstellenden höheren Vernetzungsgrade als mit der Harzlösung allein.
Claims (14)
- A prepreg, obtainable by impregnating a base paper with a thermally cross-linkable impregnation combination which contains a formaldehyde-free resin solution and a polymer dispersion, characterized in that the mixing ratio between the resin solution and the polymer dispersion in the impregnation combination amounts to from 45 : 55 to 30 : 70 (solid : solid), the residual moisture amounts to from 2 to 3% by weight, and, after drying, the prepreg has a degree of cross-linking of at least 10% and at most 85%.
- A prepreg according to Claim 1, wherein the resin solution contains:a) a polymer which is obtainable by radical polymerization and which contains, polymerized in, less than 5% by weight of an α-, β-ethylene-unsaturated mono- or dicarboxylic acid,b) a polymer which is obtainable by radical polymerization and which contains, polymerized in, more than 15% by weight of an α-, β-ethylene-unsaturated mono-or dicarboxylic acid, andc) an alkanolamine with at least two hydroxyl groups.
- A prepreg according to one of Claims 1 and 2, characterized in that the polymer dispersion is constituted on the basis of acrylic acid, acrylic acid ester, styrene, butadiene, vinyl acetate or acrylonitrile.
- A prepreg according to any one of Claims 1 to 3, characterized in that the mixing ratio between the resin solution and the polymer dispersion in the impregnation combination amounts to from 35 : 65 to 30 : 70.
- A prepreg according to any one of Claims 1 to 4, characterized in that the proportion of the impregnation components in the paper amounts to between 5 and 35% by weight with respect to the weight per unit area of the base paper.
- A prepreg according to any one of Claims 1 to 5, characterized in that the drying takes place to a residual moisture of from 2 to 3% by weight, and degrees of cross-linking of at least 50%, and preferably at least 70%, are achieved.
- A prepreg according to any one of Claims 1 to 6, characterized in that the prepreg is a decorative prepreg or a decorative coating material.
- A method of producing a prepreg, comprising the steps:a) impregnating a base paper with a thermally cross-linkable impregnation combination which contains a formaldehyde-free resin solution and a polymer dispersion, wherein the mixing ratio between the resin solution and the polymer dispersion in the impregnation combination amounts to from 45 : 55 to 30 : 70 (solid : solid), andb) drying the impregnated base paper, so that the impregnation combination has a degree of cross-linking of at least 10% and at most 85% and a residual moisture of from 2 to 3% by weight.
- A method according to Claim 8, characterized in that the resin solution contains:a) a polymer which is obtainable by radical polymerization and which contains, polymerized in, less than 5% by weight of an α-, β-ethylene-unsaturated mono- or dicarboxylic acid,b) a polymer which is obtainable by radical polymerization and which contains, polymerized in, more than 15% by weight of an α-, β-ethylene-unsaturated mono-or dicarboxylic acid, andc) an alkanolamine with at least two hydroxyl groups.
- A method according to one of Claims 8 to 9, characterized in that the drying is carried out at at least 100°C.
- A method according to any one of Claims 8 to 10, characterized in that during the impregnation the mixing ratio between the resin solution and the polymer dispersion in the impregnation combination amounts to from 35 : 65 to 30 : 70.
- A method according to any one of Claims 8 to 11, characterized in that during the impregnation the proportion of the impregnation components in the paper amounts to between 5 and 35% by weight with respect to the weight per unit area of the base paper.
- A method according to any one of Claims 8 to 12, characterized in that the drying takes place in the paper-making machine.
- A method according to any one of Claims 8 to 13, characterized in that the impregnation combination, the resin solution and/or the polymer dispersion are applied to the base paper by means of a roller-application apparatus, preferably a glue press or film press.
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EP06119238A EP1757731A3 (en) | 2003-02-24 | 2004-02-13 | Prepreg |
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DE10307966A DE10307966C5 (en) | 2003-02-24 | 2003-02-24 | Preimpregnate and process for its preparation |
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PCT/EP2004/001393 WO2004074577A1 (en) | 2003-02-24 | 2004-02-13 | Prepreg |
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US7909397B2 (en) | 2003-05-15 | 2011-03-22 | Audiovox Corporation | In-vehicle docking station for a portable media player |
EP1942141A1 (en) | 2006-12-22 | 2008-07-09 | Rohm and Haas France SAS | Curable composition |
WO2009077561A1 (en) * | 2007-12-17 | 2009-06-25 | Technocell Dekor Gmbh & Co. Kg | Compressible decorative paper impregnating agent which can be printed by the inkjet method |
DE102008014558A1 (en) | 2008-03-15 | 2009-09-17 | Dracowo Forschungs- Und Entwicklungs Gmbh | Polycarboxylic acid modified native epoxides with a specific ratio of epoxide-polycarboxylic acid in glycidyl ester epoxide, useful for preparing polyether and polyester |
EP2695745B1 (en) | 2012-08-06 | 2015-08-26 | Unilin BVBA | Method for manufacturing panels having a decorative surface |
DE102013114420A1 (en) | 2012-12-23 | 2014-06-26 | Michael Jokiel | Impregnated paper comprises base paper which is impregnated on one side with water-based impregnating solution comprising e.g. aqueous dispersion of styrene-ethyl-butyl acrylate copolymer and aqueous dispersion of styrene-acrylate copolymer |
EP2894047B1 (en) | 2014-01-10 | 2019-08-14 | Unilin, BVBA | Method for manufacturing panels having a decorative surface |
EP2905145B1 (en) | 2014-02-06 | 2019-10-23 | Unilin, BVBA | Method for manufacturing floor panels having a decorative surface |
BE1025875B1 (en) | 2018-01-04 | 2019-08-06 | Unilin Bvba | Methods for manufacturing panels |
WO2021260043A1 (en) | 2020-06-23 | 2021-12-30 | Sappi Netherlands Services B.V. | Barrier paper or board |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2949306A1 (en) † | 1979-12-07 | 1981-06-11 | Letron GmbH, 8750 Aschaffenburg | Synthetic veneer of paper fibre compsn. impregnated with resin - contg. equal wt. of long and short fibres, can be made on paper machine |
WO1994000523A1 (en) † | 1992-06-22 | 1994-01-06 | Gebrueder Buhl Papierfabriken Gmbh | Aqueous impregnating composition |
WO1995017551A1 (en) † | 1993-12-21 | 1995-06-29 | Arjo Wiggins S.A. | Impregnated sheet used as a basis for a decorative coating |
DE19728250A1 (en) † | 1997-07-02 | 1999-01-07 | Koehler Decor Gmbh & Co Kg | Production of preimpregnate for making decorative laminate |
DE19735959A1 (en) † | 1997-08-19 | 1999-02-25 | Basf Ag | Thermally curable, aqueous binding agent composition |
DE10134302C1 (en) † | 2001-07-14 | 2002-12-12 | Technocell Dekor Gmbh & Co Kg | Pre-impregnate obtained by impregnation of crude paper with a thermally hardenable formaldehyde-free resin useful in the production of decorative impregnates or coatings, and surface treatment of printed and unprinted papers |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20040039098A1 (en) * | 2002-08-22 | 2004-02-26 | Hector Belmares | Formaldehyde-free coatings and acoustical panel |
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2003
- 2003-02-24 DE DE10307966A patent/DE10307966C5/en not_active Expired - Fee Related
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2004
- 2004-02-13 ES ES04710840T patent/ES2271845T5/en not_active Expired - Lifetime
- 2004-02-13 BR BRPI0407760-1A patent/BRPI0407760B1/en not_active IP Right Cessation
- 2004-02-13 DE DE502004001322T patent/DE502004001322D1/en not_active Expired - Lifetime
- 2004-02-13 EP EP06119238A patent/EP1757731A3/en not_active Withdrawn
- 2004-02-13 AT AT04710840T patent/ATE338167T1/en not_active IP Right Cessation
- 2004-02-13 WO PCT/EP2004/001393 patent/WO2004074577A1/en active IP Right Grant
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Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2949306A1 (en) † | 1979-12-07 | 1981-06-11 | Letron GmbH, 8750 Aschaffenburg | Synthetic veneer of paper fibre compsn. impregnated with resin - contg. equal wt. of long and short fibres, can be made on paper machine |
WO1994000523A1 (en) † | 1992-06-22 | 1994-01-06 | Gebrueder Buhl Papierfabriken Gmbh | Aqueous impregnating composition |
WO1995017551A1 (en) † | 1993-12-21 | 1995-06-29 | Arjo Wiggins S.A. | Impregnated sheet used as a basis for a decorative coating |
DE19728250A1 (en) † | 1997-07-02 | 1999-01-07 | Koehler Decor Gmbh & Co Kg | Production of preimpregnate for making decorative laminate |
DE19735959A1 (en) † | 1997-08-19 | 1999-02-25 | Basf Ag | Thermally curable, aqueous binding agent composition |
DE10134302C1 (en) † | 2001-07-14 | 2002-12-12 | Technocell Dekor Gmbh & Co Kg | Pre-impregnate obtained by impregnation of crude paper with a thermally hardenable formaldehyde-free resin useful in the production of decorative impregnates or coatings, and surface treatment of printed and unprinted papers |
Non-Patent Citations (2)
Title |
---|
ARNOLD, H. ET AL: "Herstellung einseitig imprägnierter Druckpapiere mittels Filmpresse", WOCHENBLATT FÜR PARPIERFABRIKATION, June 2000 (2000-06-01), pages 350 - 355 † |
ARNOLD, H. ET AL: "Individuelles Differential Coating- bessere Bedruckbarkeit", NEUE VORIMPRÄGNATE, HOLZ- U. KUNSTSTOFF - VERARBEITUNG, June 2001 (2001-06-01), pages 36 - 38 † |
Also Published As
Publication number | Publication date |
---|---|
EP1757731A3 (en) | 2012-12-05 |
DE10307966C5 (en) | 2009-05-28 |
ES2271845T5 (en) | 2013-11-22 |
ATE338167T1 (en) | 2006-09-15 |
DE10307966A1 (en) | 2004-09-09 |
CA2518942A1 (en) | 2004-09-02 |
EP1518024B1 (en) | 2006-08-30 |
ES2271845T3 (en) | 2007-04-16 |
CA2518942C (en) | 2014-08-05 |
EP1518024A1 (en) | 2005-03-30 |
EP1757731A2 (en) | 2007-02-28 |
DE10307966B4 (en) | 2005-08-11 |
DE502004001322D1 (en) | 2006-10-12 |
BRPI0407760B1 (en) | 2014-04-22 |
BRPI0407760A (en) | 2006-10-03 |
WO2004074577A1 (en) | 2004-09-02 |
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