EP1584378A1 - Coated substrate - Google Patents
Coated substrate Download PDFInfo
- Publication number
- EP1584378A1 EP1584378A1 EP04076083A EP04076083A EP1584378A1 EP 1584378 A1 EP1584378 A1 EP 1584378A1 EP 04076083 A EP04076083 A EP 04076083A EP 04076083 A EP04076083 A EP 04076083A EP 1584378 A1 EP1584378 A1 EP 1584378A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- melamine
- formaldehyde
- coated substrate
- resin
- substrate
- 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.)
- Withdrawn
Links
- 239000000758 substrate Substances 0.000 title claims abstract description 47
- 229920000877 Melamine resin Polymers 0.000 claims abstract description 47
- 229920005989 resin Polymers 0.000 claims abstract description 25
- 239000011347 resin Substances 0.000 claims abstract description 25
- 238000000034 method Methods 0.000 claims abstract description 22
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 claims abstract description 11
- 238000010030 laminating Methods 0.000 claims abstract description 9
- 239000000049 pigment Substances 0.000 claims abstract description 7
- 230000005855 radiation Effects 0.000 claims abstract description 6
- 239000006185 dispersion Substances 0.000 claims abstract description 5
- 238000010438 heat treatment Methods 0.000 claims abstract description 5
- 238000002844 melting Methods 0.000 claims abstract description 5
- 230000008018 melting Effects 0.000 claims abstract description 5
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 15
- 239000011248 coating agent Substances 0.000 claims description 9
- 238000000576 coating method Methods 0.000 claims description 9
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 6
- 230000008569 process Effects 0.000 claims description 3
- 239000010410 layer Substances 0.000 description 33
- 229920000642 polymer Polymers 0.000 description 13
- 239000002245 particle Substances 0.000 description 9
- 239000000843 powder Substances 0.000 description 6
- 238000001035 drying Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000004132 cross linking Methods 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 239000002023 wood Substances 0.000 description 3
- FGUUSXIOTUKUDN-IBGZPJMESA-N C1(=CC=CC=C1)N1C2=C(NC([C@H](C1)NC=1OC(=NN=1)C1=CC=CC=C1)=O)C=CC=C2 Chemical compound C1(=CC=CC=C1)N1C2=C(NC([C@H](C1)NC=1OC(=NN=1)C1=CC=CC=C1)=O)C=CC=C2 FGUUSXIOTUKUDN-IBGZPJMESA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 230000004888 barrier function Effects 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000000549 coloured material Substances 0.000 description 2
- 238000003384 imaging method Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 239000004627 regenerated cellulose Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 229920002522 Wood fibre Polymers 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 230000001427 coherent effect Effects 0.000 description 1
- 239000010431 corundum Substances 0.000 description 1
- 229910052593 corundum Inorganic materials 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000009408 flooring Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 238000007641 inkjet printing Methods 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000012982 microporous membrane Substances 0.000 description 1
- 238000007645 offset printing Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000011120 plywood Substances 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 238000010020 roller printing Methods 0.000 description 1
- 230000003678 scratch resistant effect Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 238000010023 transfer printing Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D3/00—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials
- B05D3/02—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by baking
- B05D3/0254—After-treatment
- B05D3/0263—After-treatment with IR heaters
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D3/00—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials
- B05D3/12—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by mechanical means
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D2203/00—Other substrates
- B05D2203/20—Wood or similar material
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31942—Of aldehyde or ketone condensation product
- Y10T428/31949—Next to cellulosic
Definitions
- the invention relates to a method to coat a substrate with a melamine-formaldehyde resin so as to obtain good mechanical properties of the final coating. Good mechanical properties are for example required when the coated substrate is afterwards subjected to post-forming.
- the invention also relates to the coated substrate with good mechanical properties, appearance and durability, to the melamine-formaldehyde resin and to the melamine.
- a post-formable substrate is coated with a decorative barrier sheet consisting of ordinary ⁇ -cellulose wood fibre impregnated with a fully cured, unplasticized melamine-formaldehyde resin with a narrow range for the mole ratio between the formaldehyde and the melamine.
- a laminate is prepared by assembling various layers of kraft paper and a top, barrier, sheet with the unplasticized melamine-formaldehyde resin. All these carrier layers are formed into a laminate by placing the stacked layers in a laminating press under high pressure and at high temperatures during a certain amount of time.
- a disadvantage of the obtained laminates is that they cannot be bent into complex shapes along two (or more) mutually intersecting axis without breaking and/or cracking.
- a laminar prepreg which prepreg comprises one or more layers of a laminar carrier that is impregnated with an as yet uncured resin.
- the carrier is a laminar porous polymer.
- the laminar porous polymer may be a non-woven laminar polymer, a laminar open polymer foam or a microporous membrane.
- the laminar porous polymer is impregnated with the resin upon which drying is necessary at a temperature between 100 and 160 °C.
- the so obtained carrier is stacked after drying.
- the prepreg can subsequently be processed into a shaped final product by first deforming the prepreg and then curing the shaped intermediate product at elevated temperature or by combining the deformation and the curing step in one step.
- a disadvantage of the prepreg according to WO 99/13000 is that the laminar prepreg comprises at least two components that first must be obtained in separate steps: a laminar porous polymer and an (at the prepreg stage) uncured resin.
- WO00/53666 a prepreg is described that contains one or more layers of a porous carrier sheet, which porous carrier sheet has been impregnated with an as yet uncured resin, the carrier containing a meltable polymer mixed with cellulose or regenerated cellulose or mixtures there from.
- WO 00/53667 a prepreg is described that contains one or more layers of a porous carrier sheet, which porous carrier sheet has been impregnated with an as yet uncured resin, the carrier being a porous carrier on the basis of wholly or partly regenerated cellulose.
- WO 00/53688 a prepreg is described that contains one or more layers of a porous carrier sheet, which porous carrier sheet contains at least one fibrous cellulose ester.
- the method according to the invention makes it superfluous to install a separate drying section for the impregnated porous polymer. Therefore the space and apparatus necessary for the process of coating a substrate can be reduced compared to the prior art. Additionally as no drying of the impregnated porous polymer at increased temperatures is necessary in the present invention the method is advantageous from an economical and ecological point of view. Another advantage of the method according to the invention is that separate stacking of the various layers is not necessary anymore. A further advantage of the method according to the present invention is that the melamine-formaldehyde coating is applied directly onto the substrate that needs to be coated for further use, as for example worktops cupboards and fronts of kitchen cupboards. In this method a separate "prepreg stage" is absent.
- a melamine-formaldehyde resin in powder form is applied onto the surface of the substrate so as to form a layer.
- powder is here and hereinafter meant a solid consisting of small particles generally with a particle size smaller than 250 ⁇ m, preferably below 100 ⁇ m. With very large particles an even distribution over the surface of the substrate is difficult, further the resolution of the applied pattern that is formed by the ink, dye solution or pigment dispersion in step c) is worse than when smaller particles are used.
- the thickness of the layer is not particularly critical and can be chosen between wide ranges, for example between 20 and 500 ⁇ m. A preferred layer has a thickness between 50 and 250 ⁇ m.
- melamine-formaldehyde resin A is meant a resin with as main building blocks melamine and formaldehyde.
- the melamine-formaldehyde resin in A can additionally contain other building blocks, for example urea and flexibilizers as for example diethylene glycol and sugars.
- the melamine-formaldehyde resin that is used in step a) should have a glass transition temperature (Tg) high enough to be stable at room temperature as a powder for an extended period of time. In case the Tg is not high enough the resin particles will coagulate and the powder will lose its form and stability. Suitable values for the Tg are at least 30 °C, preferably 40 °C, with more preference between 60 and 90 °C.
- the Tg should be below the temperature at which steps e) and/or f) in the method are performed; as when the Tg is higher than the temperature in step e) the resin will not melt and thus it will not flow. Generally the Tg should therefore be below 140 °C, preferably lower than 120 °C.
- the melamine-formaldehyde resin A should advantageously be able to form a non-porous layer after heating and curing in step f) so as to prevent diffraction of light by included components as for example water or air. Diffraction would lead to a "blurred" pattern. This requirement can advantageously be reached by a formaldehyde-melamine ratio in the resin A between 1 and 3 (on mol basis).
- the melamine-formaldehyde resin A can be partially crosslinked before it is applied onto the substrate.
- the rate of pre-crosslinking is determined by the ability to flow. When the pre-crosslinking has proceeded too far, the resin A will not flow sufficiently and it will be impossible to remove all included components such as for example air by pressing. The man skilled in the art can easily determine the desired rate of pre-crosslinking.
- the resin A in step a) can additionally contain a pigment.
- the coating that is finally obtained has a more or less uniform colour, with no special recognizable pattern.
- the optional steps c) and d) can be left out but it may still be desirable to add in step d) a transparent topcoat layer on top of layer A to obtain a better appearance and durability.
- steps c) and d) are required.
- the resin should display such a combination of properties that the resin after the melting in step b) forms a porous layer.
- the resin particles When melting the resin particles, they flow towards each other. Depending on the circumstances during the flow phase, and given enough time, the molten particles will finally touch each other completely, thereby giving rise to a non-porous layer.
- the optional step c) it is necessary to have a layer that is still porous to some level. To keep the layer porous, the temperature during the flow-phase shouldn't be too high when the time for the flow phase is moderate. When the time available for flowing is only short, the temperature should be higher. Therefore a balance should be found between these parameters that determine the amount of flow. The man skilled in the art can easily determine the suitable conditions by routine experimentation.
- the kind of substrate depends on the final use of the coated substrate and can be for example wood or wood-based material, paper, metal, glass or plastic.
- wood-based materials are MDF (Medium Density Fibreboard) or HDF (High Density Fibreboard), OSB (oriented strand board), particle board, plywood.
- the coated substrates can be used in a large number of applications, for example serving trays, washing-up basins, crockery, doors, kitchen worktops, furniture and wall panels, kitchen cupboards, window frames, laminated flooring.
- the applied resin is being molten by IR- or NIR-radiation and can be chosen freely. It is preferred to use IR-radiation for thinner layers, for example 0-5 ⁇ m, NIR is preferably used for thicker layers for example up to 0.5 mm to ensure a favourable temperature prophile across the layer thickness.
- the duration of the radiation depends on the intensity of the radiation and the characteristics of the resin to be molten. The duration and intensity of the radiation should be such that a coherent layer is obtained, that still has a maximum porosity. This can easily be determined by routine experimentation by the man skilled in the art.
- a décor pattern is applied to the porous layer A.
- the coloured material for forming such a pattern can be an ink, or a dye solution in water, solvent or in a polymer, or a pigment dispersion in water, solvent or in a polymer.
- the coloured material can be a solid or a liquid and can be applied by any kind of imaging technique, such as off-set and roller printing, ink-jet printing, heat-transfer printing, toner printing etc as described in "Handbook of Imaging Materials” (Arthur S. Diamond ed., Marcel Dekker, 1991).
- a layer of melamine-formaldehyde resin B is applied to the coated substrate obtained after step b) or c).
- the melamine-formaldehyde resin B can be a liquid or in powder form. It is preferred to use a powderous melamine-formaldehyde resin B as in the case that it is a liquid the risk exists that the liquid will penetrate into the porous layer obtained after step b).
- the nature of the melamine-formaldehyde resin B can vary, depending on the required properties of the final coating.
- the resin B is in powderous form with a Tg in the same ranges as indicated for resin A, it preferably has a good flow at the temperature in steps e) and f) and cures into a transparent and scratch-resistant topcoat so as to make the underlying pattern visible, while also giving an excellent adhesion with the underlying layer by co-reaction in the final curing steps e) and f).
- stabilizers for example Hindered Amine Light Stabilizers (HALS), and UV absorbers can be added to resin B.
- HALS Hindered Amine Light Stabilizers
- silica and corundum can be added to the resin.
- filler particles of less than 300 nanometer are used.
- the coated substrate from step d) is heated in a laminating press for a certain amount of time.
- the absolute duration is not critical. Time and temperature are interdependent, it means that the result obtained counts but that the result can be obtained either by a high temperature and a relatively short time or by a somewhat lower temperature and a longer time. For example the time can vary between 1 and 3 minutes and the temperature can than vary between 100 and 140 °C.
- the balance between time and temperature should be chosen so as to result in a level of cure to give acceptable properties regarding the gloss and Kiton test for laminates.
- the layers A and B are pre-cured with heat before applying pressure.
- This pre-curing is done to prevent flow and absorption of the molten resin into the substrate, under the influence of pressure, which would blur the image.
- the laminating press can for example been pre-heated before the coated substrate is fed to it.
- the coated substrate can be pre-treated in a separate step so as to result in a partially cured coating. Both alternatives result in a better resolution of the pattern when a pigment, ink or dye is used in step c). It has also been found that the pre-heating or pre-treating results in a better topcoat.
- step f) the pre-cured coated substrate is subjected to increased pressure and kept under pressure for a certain amount of time.
- the time and pressure are as generally used in the field of laminates.
- the invention also relates to the melamine-formaldehyde coated substrate that is obtained with the method according to the invention It has good mechanical properties. Depending on its further use, requirements need to be met in view of for example scratch resistance, flexibility, durability, chemical resistance, abrasion resistance, cold check (that means the crack resistance at a sharp temperature change). Depending on its final use some of the above-mentioned properties are more important than others. Also depending on its further use of the coated substrate, requirements need sometimes to be met in regard of its appearance.
- the melamine-formaldehyde coated substrate that is obtained according to the invention shows improved adhesion between the coating layer and the substrate compared to the prior art laminates in which first a prepreg is made where after the prepreg is pressed onto the substrate.
- the invention further relates to the use of the melamine-formaldehyde coated substrate that is obtained according to the method of the invention in a post-forming process without structural damage to the coating.
- the invention also relates to the use of a melamine-formaldehyde resin with a formaldehyde to melamine ratio between 1-3 (on mol basis) in a method according to the invention.
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Laminated Bodies (AREA)
- Finished Plywoods (AREA)
Abstract
The invention relates to a method to coat a substrate with a melamine-formaldehyde
resin comprising the following steps:
The invention also relates to the coated substrate and its use.
Description
The invention relates to a method to coat a substrate with a
melamine-formaldehyde resin so as to obtain good mechanical properties of the final
coating. Good mechanical properties are for example required when the coated
substrate is afterwards subjected to post-forming. The invention also relates to the
coated substrate with good mechanical properties, appearance and durability, to the
melamine-formaldehyde resin and to the melamine.
In US-3.730.828 a post-formable substrate is coated with a
decorative barrier sheet consisting of ordinary α-cellulose wood fibre impregnated with
a fully cured, unplasticized melamine-formaldehyde resin with a narrow range for the
mole ratio between the formaldehyde and the melamine. A laminate is prepared by
assembling various layers of kraft paper and a top, barrier, sheet with the unplasticized
melamine-formaldehyde resin. All these carrier layers are formed into a laminate by
placing the stacked layers in a laminating press under high pressure and at high
temperatures during a certain amount of time. A disadvantage of the obtained
laminates is that they cannot be bent into complex shapes along two (or more) mutually
intersecting axis without breaking and/or cracking.
In WO 99/13000, a laminar prepreg is described which prepreg
comprises one or more layers of a laminar carrier that is impregnated with an as yet
uncured resin. The carrier is a laminar porous polymer. The laminar porous polymer
may be a non-woven laminar polymer, a laminar open polymer foam or a microporous
membrane. The laminar porous polymer is impregnated with the resin upon which
drying is necessary at a temperature between 100 and 160 °C. The so obtained carrier
is stacked after drying. The prepreg can subsequently be processed into a shaped final
product by first deforming the prepreg and then curing the shaped intermediate product
at elevated temperature or by combining the deformation and the curing step in one
step. A disadvantage of the prepreg according to WO 99/13000 is that the laminar
prepreg comprises at least two components that first must be obtained in separate
steps: a laminar porous polymer and an (at the prepreg stage) uncured resin.
In WO00/53666 a prepreg is described that contains one or more
layers of a porous carrier sheet, which porous carrier sheet has been impregnated with
an as yet uncured resin, the carrier containing a meltable polymer mixed with cellulose
or regenerated cellulose or mixtures there from. In WO 00/53667 a prepreg is
described that contains one or more layers of a porous carrier sheet, which porous
carrier sheet has been impregnated with an as yet uncured resin, the carrier being a
porous carrier on the basis of wholly or partly regenerated cellulose. In WO 00/53688 a
prepreg is described that contains one or more layers of a porous carrier sheet, which
porous carrier sheet contains at least one fibrous cellulose ester. A disadvantage of
these systems that are based on a porous polymer as a carrier and an (at the prepreg
stage) uncured resin is that at least two components are necessary in the initial stages
of the prepreg stage.
It is an object of the invention to overcome the above-mentioned
disadvantages and to make available a method to coat a substrate with a melamine-formaldehyde
resin which is less complicated than the methods in the prior art and still
results in a coated substrate with good mechanical properties.
The object is reached by a method that comprises the following
steps:
The method according to the invention makes it superfluous to install
a separate drying section for the impregnated porous polymer. Therefore the space
and apparatus necessary for the process of coating a substrate can be reduced
compared to the prior art. Additionally as no drying of the impregnated porous polymer
at increased temperatures is necessary in the present invention the method is
advantageous from an economical and ecological point of view. Another advantage of
the method according to the invention is that separate stacking of the various layers is
not necessary anymore. A further advantage of the method according to the present
invention is that the melamine-formaldehyde coating is applied directly onto the
substrate that needs to be coated for further use, as for example worktops cupboards
and fronts of kitchen cupboards. In this method a separate "prepreg stage" is absent.
In step a) of the method according to the invention a melamine-formaldehyde
resin in powder form is applied onto the surface of the substrate so as to
form a layer. With powder is here and hereinafter meant a solid consisting of small
particles generally with a particle size smaller than 250 µm, preferably below 100 µm.
With very large particles an even distribution over the surface of the substrate is
difficult, further the resolution of the applied pattern that is formed by the ink, dye
solution or pigment dispersion in step c) is worse than when smaller particles are used.
The thickness of the layer is not particularly critical and can be chosen between wide
ranges, for example between 20 and 500 µm. A preferred layer has a thickness
between 50 and 250 µm. A balance should be found between a thick layer that is
advantageous for hiding imperfections in the substrate surface, and a thin layer that is
more advantageous for post-forming. It is known to the man skilled in the art how
powders can be obtained from melamine-formaldehyde resins. Reference can for
example be made to "Kunststoff Handbuch, 10-Duroplaste" by W. Becker, D. Braun,
1988 Carl Hanser Verlag; more specifically to the chapter "Melaminharze", page 41
and further.
With melamine-formaldehyde resin A is meant a resin with as main
building blocks melamine and formaldehyde. The melamine-formaldehyde resin in A
can additionally contain other building blocks, for example urea and flexibilizers as for
example diethylene glycol and sugars.
The melamine-formaldehyde resin that is used in step a) should have
a glass transition temperature (Tg) high enough to be stable at room temperature as a
powder for an extended period of time. In case the Tg is not high enough the resin
particles will coagulate and the powder will lose its form and stability. Suitable values
for the Tg are at least 30 °C, preferably 40 °C, with more preference between 60 and
90 °C. The Tg should be below the temperature at which steps e) and/or f) in the
method are performed; as when the Tg is higher than the temperature in step e) the
resin will not melt and thus it will not flow. Generally the Tg should therefore be below
140 °C, preferably lower than 120 °C.
The melamine-formaldehyde resin A should advantageously be able
to form a non-porous layer after heating and curing in step f) so as to prevent diffraction
of light by included components as for example water or air. Diffraction would lead to a
"blurred" pattern. This requirement can advantageously be reached by a formaldehyde-melamine
ratio in the resin A between 1 and 3 (on mol basis). Optionally the melamine-formaldehyde
resin A can be partially crosslinked before it is applied onto the
substrate. Depending on the precise composition of the melamine-formaldehyde resin
A, the rate of pre-crosslinking is determined by the ability to flow. When the pre-crosslinking
has proceeded too far, the resin A will not flow sufficiently and it will be
impossible to remove all included components such as for example air by pressing.
The man skilled in the art can easily determine the desired rate of pre-crosslinking.
The resin A in step a) can additionally contain a pigment. In that case
the coating that is finally obtained has a more or less uniform colour, with no special
recognizable pattern. In case that such a uniform coloured layer is required the optional
steps c) and d) can be left out but it may still be desirable to add in step d) a
transparent topcoat layer on top of layer A to obtain a better appearance and durability.
When a décor pattern in the coating is desired steps c) and d) are required.
The resin should display such a combination of properties that the
resin after the melting in step b) forms a porous layer. When melting the resin particles,
they flow towards each other. Depending on the circumstances during the flow phase,
and given enough time, the molten particles will finally touch each other completely,
thereby giving rise to a non-porous layer. However for the optional step c) it is
necessary to have a layer that is still porous to some level. To keep the layer porous,
the temperature during the flow-phase shouldn't be too high when the time for the flow
phase is moderate. When the time available for flowing is only short, the temperature
should be higher. Therefore a balance should be found between these parameters that
determine the amount of flow. The man skilled in the art can easily determine the
suitable conditions by routine experimentation.
The kind of substrate depends on the final use of the coated
substrate and can be for example wood or wood-based material, paper, metal, glass or
plastic. Examples of wood-based materials are MDF (Medium Density Fibreboard) or
HDF (High Density Fibreboard), OSB (oriented strand board), particle board, plywood.
The coated substrates can be used in a large number of applications, for example
serving trays, washing-up basins, crockery, doors, kitchen worktops, furniture and wall
panels, kitchen cupboards, window frames, laminated flooring.
In step b) of the method according to the invention the applied resin
is being molten by IR- or NIR-radiation and can be chosen freely. It is preferred to use
IR-radiation for thinner layers, for example 0-5 µm, NIR is preferably used for thicker
layers for example up to 0.5 mm to ensure a favourable temperature prophile across
the layer thickness. The duration of the radiation depends on the intensity of the
radiation and the characteristics of the resin to be molten. The duration and intensity of
the radiation should be such that a coherent layer is obtained, that still has a maximum
porosity. This can easily be determined by routine experimentation by the man skilled
in the art.
In step c) a décor pattern is applied to the porous layer A. The
coloured material for forming such a pattern can be an ink, or a dye solution in water,
solvent or in a polymer, or a pigment dispersion in water, solvent or in a polymer. The
coloured material can be a solid or a liquid and can be applied by any kind of imaging
technique, such as off-set and roller printing, ink-jet printing, heat-transfer printing,
toner printing etc as described in "Handbook of Imaging Materials" (Arthur S. Diamond
ed., Marcel Dekker, 1991).
In step d) a layer of melamine-formaldehyde resin B is applied to the
coated substrate obtained after step b) or c). The melamine-formaldehyde resin B can
be a liquid or in powder form. It is preferred to use a powderous melamine-formaldehyde
resin B as in the case that it is a liquid the risk exists that the liquid will
penetrate into the porous layer obtained after step b). The nature of the melamine-formaldehyde
resin B can vary, depending on the required properties of the final
coating. Preferably the resin B is in powderous form with a Tg in the same ranges as
indicated for resin A, it preferably has a good flow at the temperature in steps e) and f)
and cures into a transparent and scratch-resistant topcoat so as to make the underlying
pattern visible, while also giving an excellent adhesion with the underlying layer by co-reaction
in the final curing steps e) and f). In order to protect the underlying layer(s)
from environmental influences and degradation, stabilizers for example Hindered
Amine Light Stabilizers (HALS), and UV absorbers can be added to resin B. In addition,
to ensure a better scratch resistance inorganic fillers for example clay, silica and
corundum can be added to the resin. Preferably, for the purpose of maintaining the
optical transparency, filler particles of less than 300 nanometer are used.
Subsequently the coated substrate from step d) is heated in a
laminating press for a certain amount of time. The absolute duration is not critical. Time
and temperature are interdependent, it means that the result obtained counts but that
the result can be obtained either by a high temperature and a relatively short time or by
a somewhat lower temperature and a longer time. For example the time can vary
between 1 and 3 minutes and the temperature can than vary between 100 and 140 °C.
The balance between time and temperature should be chosen so as to result in a level
of cure to give acceptable properties regarding the gloss and Kiton test for laminates.
Advantageously the layers A and B are pre-cured with heat before
applying pressure. This pre-curing is done to prevent flow and absorption of the molten
resin into the substrate, under the influence of pressure, which would blur the image.
For this purpose, the laminating press can for example been pre-heated before the
coated substrate is fed to it. Alternatively the coated substrate can be pre-treated in a
separate step so as to result in a partially cured coating. Both alternatives result in a
better resolution of the pattern when a pigment, ink or dye is used in step c). It has also
been found that the pre-heating or pre-treating results in a better topcoat.
In step f) the pre-cured coated substrate is subjected to increased
pressure and kept under pressure for a certain amount of time. The time and pressure
are as generally used in the field of laminates.
The invention also relates to the melamine-formaldehyde coated
substrate that is obtained with the method according to the invention It has good
mechanical properties. Depending on its further use, requirements need to be met in
view of for example scratch resistance, flexibility, durability, chemical resistance,
abrasion resistance, cold check (that means the crack resistance at a sharp
temperature change). Depending on its final use some of the above-mentioned
properties are more important than others. Also depending on its further use of the
coated substrate, requirements need sometimes to be met in regard of its appearance.
The melamine-formaldehyde coated substrate that is obtained
according to the invention shows improved adhesion between the coating layer and the
substrate compared to the prior art laminates in which first a prepreg is made where
after the prepreg is pressed onto the substrate.
The invention further relates to the use of the melamine-formaldehyde
coated substrate that is obtained according to the method of the
invention in a post-forming process without structural damage to the coating.
The invention also relates to the use of a melamine-formaldehyde
resin with a formaldehyde to melamine ratio between 1-3 (on mol basis) in a method
according to the invention.
Claims (5)
- Method to coat a substrate with a melamine-formaldehyde resin comprising the following steps:a) Applying a layer of powderous melamine-formaldehyde A resin to a substrate,b) Melting the melamine-formaldehyde resin by IR- or NIR- radiation,c) Optionally applying an ink, dye solution or pigment dispersion to the with molten melamine-formaldehyde resin coated substrate,d) Optionally applying a layer of melamine-formaldehyde resin B to the coated substrate from step b) or c),e) Optionally heating the coated substrate from the previous steps in a laminating press for a certain amount of time,f) Increasing the pressure in the laminating press and keeping the laminate under pressure for a certain amount of time.
- Melamine-formaldehyde coated substrate obtainable by the method according to claim 1.
- Melamine-formaldehyde coated substrate with improved adhesion between the coating and the substrate.
- Use of the melamine-formaldehyde coated substrate according to claim 2 or 3 in a post-forming process. Melamine-formaldehyde resin with a melamine to formaldehyde ratio between 2-3 (on mol basis).
- Use of a melamine-formaldehyde resin with a melamine to formaldehyde ratio between 2-3, in a method according to claim 1.
Priority Applications (13)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP04076083A EP1584378A1 (en) | 2004-04-08 | 2004-04-08 | Coated substrate |
TW094111061A TW200613067A (en) | 2004-04-08 | 2005-04-07 | Coated substrate |
CNA200580011919XA CN1942255A (en) | 2004-04-08 | 2005-04-08 | Coated substrate |
CA 2559795 CA2559795A1 (en) | 2004-04-08 | 2005-04-08 | Coated substrate |
JP2007507262A JP2007532343A (en) | 2004-04-08 | 2005-04-08 | Coated substrate |
MYPI20051570A MY145516A (en) | 2004-04-08 | 2005-04-08 | Coated substrate |
PCT/NL2005/000272 WO2005097874A2 (en) | 2004-04-08 | 2005-04-08 | Coated substrate |
AU2005230952A AU2005230952A1 (en) | 2004-04-08 | 2005-04-08 | Coated substrate |
EP20050737677 EP1735112A2 (en) | 2004-04-08 | 2005-04-08 | Coated substrate |
EA200601878A EA011590B1 (en) | 2004-04-08 | 2005-04-08 | Coated substrate |
BRPI0509615-4A BRPI0509615A (en) | 2004-04-08 | 2005-04-08 | method for coating a substrate, coated substrate, use of a coated substrate and dispersion of liquid or solid melamine-formaldehyde particles in a liquid |
US10/594,395 US20070224438A1 (en) | 2004-04-08 | 2005-04-08 | Coated Substrate |
NO20065139A NO20065139L (en) | 2004-04-08 | 2006-11-07 | Coated substrate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP04076083A EP1584378A1 (en) | 2004-04-08 | 2004-04-08 | Coated substrate |
Publications (1)
Publication Number | Publication Date |
---|---|
EP1584378A1 true EP1584378A1 (en) | 2005-10-12 |
Family
ID=34896061
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP04076083A Withdrawn EP1584378A1 (en) | 2004-04-08 | 2004-04-08 | Coated substrate |
EP20050737677 Withdrawn EP1735112A2 (en) | 2004-04-08 | 2005-04-08 | Coated substrate |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP20050737677 Withdrawn EP1735112A2 (en) | 2004-04-08 | 2005-04-08 | Coated substrate |
Country Status (12)
Country | Link |
---|---|
US (1) | US20070224438A1 (en) |
EP (2) | EP1584378A1 (en) |
JP (1) | JP2007532343A (en) |
CN (1) | CN1942255A (en) |
AU (1) | AU2005230952A1 (en) |
BR (1) | BRPI0509615A (en) |
CA (1) | CA2559795A1 (en) |
EA (1) | EA011590B1 (en) |
MY (1) | MY145516A (en) |
NO (1) | NO20065139L (en) |
TW (1) | TW200613067A (en) |
WO (1) | WO2005097874A2 (en) |
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Also Published As
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EA011590B1 (en) | 2009-04-28 |
MY145516A (en) | 2012-02-29 |
TW200613067A (en) | 2006-05-01 |
WO2005097874A3 (en) | 2006-03-02 |
BRPI0509615A (en) | 2007-09-18 |
US20070224438A1 (en) | 2007-09-27 |
AU2005230952A1 (en) | 2005-10-20 |
CA2559795A1 (en) | 2005-10-20 |
NO20065139L (en) | 2007-01-08 |
WO2005097874A2 (en) | 2005-10-20 |
EP1735112A2 (en) | 2006-12-27 |
CN1942255A (en) | 2007-04-04 |
EA200601878A1 (en) | 2007-02-27 |
JP2007532343A (en) | 2007-11-15 |
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