(19)
(11)EP 0 136 577 B1

(12)EUROPEAN PATENT SPECIFICATION

(45)Mention of the grant of the patent:
15.02.1989 Bulletin 1989/07

(21)Application number: 84110472.2

(22)Date of filing:  04.09.1984
(51)International Patent Classification (IPC)4B32B 3/00, B32B 27/10, B32B 33/00

(54)

Decorative laminate having mar-resistant surface

Dekorative Mehrschichtstoffe mit kratzfester Oberfläche

Laminé décoratif résistant à l'abrasion


(84)Designated Contracting States:
AT BE CH DE FR GB IT LI LU NL SE

(30)Priority: 03.10.1983 US 538626

(43)Date of publication of application:
10.04.1985 Bulletin 1985/15

(73)Proprietor: FORMICA CORPORATION
Wayne New Jersey 07470 (US)

(72)Inventor:
  • Hosler, John Frederick
    Cincinnati Ohio (US)

(74)Representative: Klunker . Schmitt-Nilson . Hirsch 
Winzererstrasse 106
80797 München
80797 München (DE)


(56)References cited: : 
US-A- 4 255 480
  
     
    Remarks:
    The file contains technical information submitted after the application was filed and not included in this specification
     
    Note: Within nine months from the publication of the mention of the grant of the European patent, any person may give notice to the European Patent Office of opposition to the European patent granted. Notice of opposition shall be filed in a written reasoned statement. It shall not be deemed to have been filed until the opposition fee has been paid. (Art. 99(1) European Patent Convention).


    Description


    [0001] The present invention relates to a heat and pressure consolidated decorative laminate according to the preamble of claim 1. Such a decorative laminate is known from US-A-3,525,664.

    [0002] For many years, decorative laminates have been used as a surfacing material in residential and commercial applications. Typical applications are surfacing for walls, partitions, table tops, counter tops, furniture, doors and the like. Decorative laminates of this type are usually produced by high pressure or low pressure methods depending upon the ultimate usage contemplated, the laminates produced utilizing high pressure techniques usually exhibiting superior properties.

    [0003] High pressure decorative laminates are made of three essential layers: a core layer, a print layer, and an optional surface layer. The core layer constitutes a bottom or supporting layer onto which the other layers are bonded. In normal high-pressure laminate manufacture the core layer consists of a plurality of resin impregnated kraft paper sheets. Laminating resins commonly used include phenolic, amino, epoxy, polyester resins and the like. The industrially preferred laminating resin for decorative laminates is a phenolic resin. In low-pressure laminate manufacture, the core layer is generally comprised of a sheet of particleboard ranging from 0.95 to 2.54 cm (3/8" to 1") in thickness.

    [0004] Placed above the core layer is the print layer which is generally an alpha cellulose containing pigmented paper carrying a print, pattern, or design that has been impregnated with a melamine- formaldehyde resin.

    [0005] The cured melamine-formaldehyde resins are colorless, resistant to light, solvents and stains and their heat resistance makes them immune to burning cigarettes, boiling water and heated containers up to about 162,78°C (325°F).

    [0006] The surface layer, or overlay, is a high-quality alpha cellulose containing paper impregnated with a melamine-formaldehyde resin. This layer is optional and protects the print sheet from external abuse such as abrasive wear and tear, harsh chemicals, burns, spills and the like. It is primarily the melamine- formaldehyde resin which accounts for these protective properties.

    [0007] The core material, print layer and optional surface layer are stacked in a superimposed relationship, between stainless steel plates and subjected to a pressure and temperature for a time sufficiently long enough to cure the laminating resins impregnating the respective layers. The elevated temperatures and pressure actually cause the impregnated resins within the sheets to flow and thereby consolidate the layers into an integral mass.

    [0008] For obvious economic reasons, it is common practice, when producing the paper supported laminates, to consolidate a plurality of these individual laminating assemblies into one large assembly, or press pack, said stacks being separated from one another by a release sheet, and then to laminate this pack by heat and pressure application.

    [0009] In consolidating the laminate components according to most widely practiced techniques, an individual assembly is placed with its decorative overlayment surface adjacent to a highly polished stainless steel press plate. The function of the press plate is twofold. First, it provides a smooth, defect-free surface to one side of the laminate. Second, in connection with the paper based supported systems, it serves to separate pairs of back-to-back assemblies, thus permitting a plurality of these assemblies to be consolidated into laminates in one operation, usually in back-to-back relationship.

    [0010] The heat and pressure consolidation of the laminate assemblies into useful laminates utilizing smooth, polished plates, results in the production of laminates having very glossy surfaces. When less glossy surfaces are required, an aluminum caul stock or a textured plate can be used to impart less glossy surfaces to the laminates.

    [0011] As the decorative laminate art progressed, technicians continually strived to improve upon the aesthetics and properties of the high pressure and low pressure decorative laminates. One area where no significant developments have occurred is with regards to the mar-resistance of the laminate. Mar-resistance refers to the ability of the uppermost laminate surface to resist damage due to incidental or accidental contact thereof with an extraneous object. The propensity for laminate surfaces to exhibit poor mar-resistance is greater for laminates having high gloss surfaces than low gloss surfaces, especially where the decor sheet of the laminate is a solid color, and even more especially where the solid color is dark, e.g. navy blue, brown or black. Decorative laminates of this type show the "wear and tear" of everyday use more than laminates of a solid pastel color or laminates having a matte finish, regardless of which decorative pattern is employed.

    [0012] Thus, there exists a need for increasing the mar-resistance of decorative laminates, the fulfillment of which would satisfy a long felt need in the art.

    Summary of the invention



    [0013] The present invention provides decorative laminates of increased mar-resistance by the incorporation of mineral particles into the uppermost surface of the laminate. The use of very small mineral particles in the production of abrasion resistant decorative laminates is well known, (see U.S. Patent 3,525,664). However, this patent generally employs the use of much more of the mineral particles than used in the present invention and does not require that the particles be positioned in the outermost confines of the laminate surface. Additionally, known abrasion resistant laminates employ particles of a size much larger than useful herein. See U.S. Patent Nos. 3,135,643; 3,445,327; 3,798,111; 4,263,081; 4,327,141; 4,305,987; 4,395,452; 4,255,480. It has been found that by following the teachings of the present invention, laminates having increased mar-resistance as opposed to increased abrasion-resistance can be produced.

    [0014] The present invention is directed to a heat and pressure consolidated decorative laminate comprising, in superimposed relationship,

    (a) a self-supporting substrate,

    (b) a thermoset resin impregnated decorative sheet, and

    (c) an optional thermoset resin impregnated overlay sheet, the outermost surface of said laminate containing mineral particles, characterized in that said particles have a Mohs hardness of at least 5 and range in size from 5 to 100 nm and are positioned within the outermost 25 pm of said laminate thickness and in an amount ranging from 0.5 to 25 grams/m2 of laminate surface area.



    [0015] As mentioned above, the self-supporting substrate may constitute any material known for this purpose with such materials of particleboard, chipboard, flakeboard, and the like being used in the production of low pressure laminates and resin impregnated kraft paper sheets (1-11 in number) being used in the production of high pressure laminates.

    [0016] The decorative sheets are also well known, as mentioned above, and generally constitute alpha-cellulose containing, pigmented and/or printed paper sheets impregnated with a nobel thermoset resin such as melamine/formaldehyde resin, urea/formaldehyde resin, polyester resin and the like.

    [0017] The optional overlay sheet, as discussed above, is equally well known and also comprises alpha-cellulose containing paper impregnated with a nobel thermoset resin such as melamine/ formaldehyde resin or those listed above, and when formed into the laminate, is a transparent, allowing the decorative pattern of the decor sheet to show through the laminate surface. These overlay sheets used in the practice of the present invention may contain abrasion resistant additives, such as hard particles of 20-50 pm size, to impart abrasion resistance to the laminate as is known in the art as represented by the above-mentioned patents.

    [0018] The outermost surface of the laminates of the present invention i.e. immediately above the decor sheet in low pressure laminates or high pressure laminates devoid of an overlay sheet, or immediately above the overlay sheet, when used, in high pressure laminates, has positioned therewithin hard, mineral particles. These particles generally having a Mohs hardness of at least 5, preferably at least 9, are utilized in the form of a colloidal dispersion and range in size from 5-100 nm, preferably from 20-60 nm. They end up in the laminate within the outermost 25 11m of the laminate thickness, preferably within the outermost 15 11m, and in an amount ranging from 0.5 to 25 grams per square meter of the laminate surface area, preferably from 1 to 10 grams per square meter. When lower concentrations of particulate material are employed, considerably less mar-resistance is imparted to the laminate and when higher concentrations are employed, the mar-resistance remains essentially constant, however, the laminates may exhibit graying and loss of gloss.

    [0019] The mineral particles are incorporated into the laminate by spraying them, as a colloidal dispersion, onto the paper sheet which will form the outermost (uppermost) laminate component before said sheet is impregnated with resin, or after said sheet is impregnated with resin and before it is thereafter dried or, preferably, after said sheet is impregnated with resin and after it is thereafter dried.

    [0020] Any particulate material conforming to the specifications specified above may be used, with such materials as silica, alumina, titanium oxide, tin oxide, zirconium oxide, antimony oxide, cerium oxide, diamond, alumina coated on silica, zirconia on silica, and the like, being exemplary.

    [0021] When producing the novel laminates of the present invention, a thermosetting resin impregnated component sheet is formed containing the mineral particles in the manner and amount specified above. The resultant component sheet is positioned, with the mineral particle side facing outwardly, i.e. as the outermost (topmost) component of the decorative laminate assembly, and the assembly is heat and pressure consolidated as is known in the art.

    [0022] The recovered laminate exhibits excellent mar-resistance attributable to the millimicron sized particles at the laminate surface. High gloss laminates retain their high gloss and matte or texturized laminates retain their same surface aesthetics as when the particles are absent. The laminates, however, when marred, retain a greater degree of their original surface gloss for a period longer than laminates devoid of the mineral particles.

    [0023] The instant laminates may or may not be produced with the aid of extraneous binders such as microcrystalline cellulose, carboxy methyl cellulose, silane coupling agents, etc.

    [0024] The incorporation of the mineral particles in accordance with the present invention does not significantly change or otherwise alter any of the necessary or desired performance properties of the laminates produced and, surprisingly, does not disadvantageously increase tool wear, an undesirable property which usually accompanies the addition of hard particles to laminates.

    [0025] The colloidal dispersion of the mineral particles can be applied to the laminate sheet by any suitable means such as by spraying, knife coating, roll coating, gravure coating, silk screening, Maier bar and the like.

    [0026] The following examples are set forth for purposes of illustration only and are not to be construed as limitations on the present invention except as set forth in the appended claims. All parts and percentages are by weight unless otherwise specified.

    [0027] In the following examples, there is a distinction made between mar-resistance and abrasion resistance. Mar-resistance is measured by the Mar-Resistance test specified below whereas abrasion resistance is measured using NEMA test LD 3-3.01. In the NEMA test, a laminate sample is clamped on a rotating disc, over which ride two weighted rubber wheels, faced with calibrated sandpaper strips. As the laminate surface is rotated under the wheels, the abrasive action of the sandpaper cuts through the surface of the laminate and gradually through the overlay until the printed pattern is exposed and destroyed. The NEMA standard for TYPE I laminate requires that the laminate, after four hundred rotation cycles, have no more than 50% of its pattern destroyed. The 50% end point is estimated by averaging the number of cycles at which the pattern shows initial wear, and the number of cycles at which the pattern is completely destroyed.

    [0028] In the Mar-Resistance test, a first scratch mar is made on a first area of the test laminate surface with ten double-rubs using a fresh Scotch-Brite@ scour/pad (3M type 8A Standard Green Household-very fine cleaning and finishing containing AI203 as the abrasive) and a second scratch mar is made on a second area of the test laminate surface with another ten rubs using the same section of the previously used pad. Any dust created is removed, preferably with a paper towel moistened with water and dried. Following this procedure, a portable, digital readout 60° Gardner gloss meter as described in NEMA test LD 3-3.13(2.0) is calibrated in accordance with NEMA test LD 3-3.13 (4.0) and placed on the sample background. The maximum background gloss is recorded and the meter is moved slowly across the first scratch mar. The minimum gloss observed is recorded, the meter is moved to the next background area, the maximum background gloss is again recorded and the meter is finally moved over the second scratch mar where the minimum gloss is again recorded. The maximum background glosses are averaged, the minimum scratch mar glosses are averaged and the difference between the two averages is determined. The difference is then divided by the average background gloss. The result, times one hundred, is expressed as percentage loss of gloss. Fresh pads are used for each test (a test is two ten-double-rub marks on a given specimen). Test apparatus is AATCC Crockmeter Model CM-1, Atlas Electric Devices, Chicago, lll., with 0.908 kg (2 lb.) load on 20 mm square pad.

    [0029] In the following examples, various commercially available particulate mineral colloidal dispersions are used to impart mar-resistance to the surface of decorative laminates. The different dispersions used are identified and set forth below in Table I.

    Examples 1-15

    [0030] Colloidal mineral dispersions, as described in Table I, are sprayed onto dry, melamine/formaldehyde resin impregnated solid navy blue decorative sheets. The sprayed sheets are dried to remove the dispersion medium, weighed and each individually are positioned atop six (6) sheets of phenol/ formaldehyde resin impregnated, dry kraft paper sheets. The superimposed sheets are then heat and pressure consolidated into decorative laminates using polished stainless steel press plates. The resultant laminates are mar-resistance tested, as described above. The results are set forth in Table II, below. The polished steel plates are not scratched or otherwise affected at any gsm coating level used. A microscopic study, using X-Ray Emission Spectra, of the resultant laminates shows that all of the silica particles are contained within the outermost 15 µm of the laminate thickness.



    [0031] As can be seen from Examples 14 and 15, when compared to Examples 1, 2,12 and 13, an increase in the amount of added particles over an optimum maximum, does not materially alter the Gloss Loss achieved.

    Examples 16-32



    [0032] Following the procedure of Examples 1-15, above, except that the colloidal dispersions are gravure coated onto the resin impregnated, dry decor sheet, the mar-resistance test results set forth in Table III, below, are achieved. Again, the steel press plates are not material affected and the particles are determined to be contained in the outermost 15 pm of the laminate thickness.


    Examples 33-43



    [0033] Again the procedure of Examples 1-15 is followed, except that the colloidal dispersions are gravure coated onto the melamine resin impregnated, dry sheets and the press plates are etched with a suede finish. The mar-resistance test results are set forth in Table IV, below. No plate damage is discerned. Detection shows the particles to be in the upper 15 µm of the laminate thickness.


    Examples 44-46



    [0034] Colloidal mineral dispersions are gravure coated onto dry, melamine/formaldehyde impregnated, a-cellulose containing overlay sheets (containing about 25 pm diameter abrasive particles) and dried. The resultant sheets are individually positioned atop a dry, melamine/formaldehyde impregnated solid brown agate decor sheet which, in turn, is positioned atop five (5) phenolic resin impregnated kraft paper sheets. The assemblies are pressed into laminates having a high gloss surface. The laminates are examined and show the silica particles to be in the top 25 pm thereof. Examination of the stainless steel, polished press plates reveals no discernable damage. The mar-resistance test results recorded upon testing the laminate samples are set forth in Table V, below.


    Example 47



    [0035] Colloidal Dispersion B is blended with microcrystalline cellulose and carboxy methyl cellulose. The resultant aqueous suspension contains 33% silica, 3.5% microcrystalline cellulose, 0.5% carboxymethyl cellulose and 63% water. The suspension is Maier Bar coated onto the dry, resin impregnated decor paper of Examples 1-15 and formed into a laminate as set forth therein. The percent Gloss Loss for the laminate as per the above mar-resistance test, which contains 26.4 g/m2 of silica, is 9.0.

    Example 48



    [0036] The dry, resin impregnated decor paper of Examples 1-15 is coated with a 5% aqueous suspension of microcrystalline cellulose and carboxymethyl cellulose (7:1 ratio, respectively) using a Maier Bar and dried. A coating (4.6 g/m2) of microcrystalline cellulose is then applied. The resultant sheet is next sprayed with Colloidal Dispersion B to deposit 22.7 g/m2 of silica. The percent Gloss Loss (determined using above described mar-resistance test) of the resultant laminate, formed as in Examples 1-15, is 8.8.

    Example 49-51



    [0037] Colloidal Dispersion F is blended with a commercially available dry melamine/formaldehyde resin to produce a suspension comprising 21.4% silica dioxide, 28.6% melamine resin, 28.6% isopropanol and 21.4% water. Following the procedure of Examples 1-15, this suspension is Maier Bar coated onto three dry, melamine/formaldehyde resin impregnated Navy blue decor sheets and each is formed into a laminate. The mar-resistance test results are set forth in Table VI, below.


    Examples 52-64



    [0038] Following the procedure of Examples 1-15, Colloidal Dispersion B is spray coated onto a series of differently colored, dry, melamine/formaldehyde resin impregnated decor sheets and formed into laminates. No plate scratching or other marring can be seen. Examination shows the silica particles to be within the top 20 µm of the laminates. The results of the mar-resistance test conducted on the laminates are set forth in Table VII, below.


    Examples 65-67



    [0039] In order to evaluate the effect of applying the particulate material to the topmost sheet at various stages of the resin impregnation and drying of said sheet, the decor paper of Examples 1-15 is impregnated with a commercially available melamine/formaldehyde resin to a resin content of 52% (on treated weight) and Colloidal Dispersion B is sprayed onto the paper at a 10 g/m2 level according to the following procedures and mar-resistance tested, after formation of the laminate, for Gloss Loss. The results are set forth in Table VIII, below.

    Example 68 (Comparative)

    [0040] When the procedure of Examples 1-15 is again followed except that the particle size of the silica particles (in a water suspension) average 2-9 pm and the decor sheet is colored black, a Gloss Loss of 10% or lower is achieved when 4 or more g/m2 of the particles are sprayed on the decor paper. When more than 4 g/m2 are employed, the laminate surfaces exhibit a greying, however, at all g/m2 levels of silica, the highly polished plates of the laminate press show evidence of scratching.

    Examples 69-71 (Comparative)



    [0041] Following the procedure described in U.S. Patent No. 3,525,644 (Sample G of Table II) a formulation is prepared from 200 parts of a commercially available melamine/formaldehyde resin, 240 parts of water, 10 parts of isopropanol and 160 parts of Colloidal Dispersion C. Navy blue decor paper is impregnated with the resultant formulation in accordance with said patent, formed into laminates which are tested in accordance with the mar-resistance and abrasion tests discussed above and compared to laminates void of any impregnated silica particles. The results are set forth in Table IX, below.



    [0042] As can be seen, the teachings of U.S. Patent 3,525,644 result in the production of laminates exhibiting an increased abrasion resistance as disclosed therein, however, application of the silica particles to the decor sheet from an impregnating resin bath, does not materially increase the mar-resistance of the laminate produced therefrom even when high concentrations of silica are applied since the majority of the silica particles are not situated within the outermost 25 µm of the laminate thickness.

    Examples 72-76



    [0043] The procedure of Examples 1-15 is again followed except that brown decor paper is first conditioned to 50% RH, spray coated with Colloidal Dispersion F and reconditioned to 50% RH before being formed into a laminate. Various concentrations of silica particles are applied using this technique. The mar-resistance test results of these laminates are set forth below in Table X.


    Examples 77-82



    [0044] Following the procedure of Examples 72-76 except that the decor sheet is black and Colloidal Dispersion B is used, the following mar-resistance test results are recorded. (Table XI).


    Examples 83-87



    [0045] Again following the procedure of Examples 72-76 except that Colloidal Dispersion C is used and the decor paper is black, the following mar-resistance test results are recorded. (Table XII).


    Examples 88-93



    [0046] The procedure of Examples 72-76 is again followed except that the decor sheet is black and Colloidal Dispersion I is used. Results are shown in Table XIII, below.


    Example 94



    [0047] The procedure of Examples 1-15 is again followed except that the phenolic resin core sheets are replaced by a 1.905 cm (3/4 inch) thick, smooth surface particleboard. Similar Gloss Loss results are achieved.

    Examples 95-100



    [0048] A dry, a-cellulose containing solid white decorative sheet and a dry, a-cellulose containing woodgrain decorative sheet, each impregnated with about 56% (based on total weight) of a commercially available polyester resin, are coated with Colloidal Dispersion B to a pick-up of 3 gsm silica and dried. The resultant sheets are positioned atop 6 sheets of phenol/formaldehyde resin impregnated dry kraft paper sheets and heat and pressure consolidated into decorative laminates using polished steel plates or plates etched with a suede finish. Uncoated control laminates are processed similarly. The results of the mar-resistance test are set forth in Table XIV, below. The silica particles are situated within the top 25 pm of the laminate thickness. No press plate damage is detected.




    Claims

    1. A heat and pressure consolidated decorative laminate comprising, in superimposed relationship,

    (a) a self-supporting substrate,

    (b) a thermoset resin impregnated decorative sheet, and

    (c) an optional thermoset resin impregnated overlay sheet,

    the outermost surface of said laminate containing mineral particles, characterized in that said particles have a Mohs hardness of at least 5 and range in size from 5 to 100 nm and are positioned within the outermost 25 µm of said laminate thickness and in an amount ranging from 0.5 to 25 grams/m2 of laminate surface area.
     
    2. A decorative laminate according to Claim 1 wherein said mineral is silica.
     
    3. A decorative laminate according to Claim 1 wherein the particle size of said mineral ranges from 20 to 60 nm.
     
    4. A decorative laminate according to Claim 1 wherein said mineral particles are present in the outermost 15 pm of the laminate thickness.
     
    5. A decorative laminate according to Claim 1 wherein the amount of mineral particles present in said laminate surface ranges from 1 to 10 grams per square meter of laminate area.
     
    6. A method for the preparation of a decorative laminate according to one of Claims 1 to 5 which comprises:

    a) forming a thermosetting resin impregnated component sheet containing mineral particles, as defined in claim 1

    b) positioning said component sheet, with its particle surface upward, as the uppermost component of a decorative laminate assembly and

    c) heat and pressure consolidating said assembly, whereby said particles are positioned within the outermost 25 pm of the thickness of the resultant laminate.


     


    Ansprüche

    1. Durch Hitze und Druck verbundenes, dekoratives Laminant das, übereinander gelagert,

    (a) ein selbsttragendes Substrat,

    (b) ein dekoratives Flachmaterial, das mit Hitze gehärtetem Harz imprägniert ist, und

    (c) ein wahlfreies Oberflächen-Flachmaterial enthält, das mit einem hitzegehärteten Harz imprägniert ist,

    wobei die äußerste Oberfläche des Laminats Mineralstoffpartikel enthält, dadurch gekennzeichnet, daß die Partikel eine Mohs-Härte von mindestens 5 haben und im Grössenbereich von 5-100 nm liegen und innerhalb der äußersten 25 11m der Laminatdicke angeordnet sind und in einer Menge im Bereich von 0,5-25 g/m2 Laminatoberfläche vorhanden sind.
     
    2. Dekoratives Laminat nach Anspruch 1, dadurch gekennzeichnet, daß der Mineralstoff Kieselerde ist.
     
    3. Dekoratives Laminat nach Anspruch 1, dadurch gekennzeichnet, daß die Teilchengröße des Mineralstoffes im Bereich von 20-60 nm liegt.
     
    4. Dekoratives Laminat nach Anspruch 1, dadurch gekennzeichnet, daß die Mineralstoffpartikel in den äußersten 15 um der Laminatdicke vorhanden sind.
     
    5. Dekoratives Laminat nach Anspruch 1, dadurch gekennzeichnet, daß die Menge an Mineralstoffpartikeln, die in der Laminatoberfläche vorhanden sind, im Bereich von 1-10 g/m2 Laminatfläche liegt.
     
    6. Verfahren zur Herstellung eines dekorativen Laminats nach einem der Ansprüche 1-5, das folgende Schritte enthält:

    (a) Bilden eines mit hitzegehärtetem Harz imprägnierten Teil-Flachmaterials, das Mineralstoffpartikel, wie in Anspruch 1 definiert, enthält,

    (b) Anordnen des Teil-Flachmaterials, wobei seine Teilchenoberfläche nach oben gerichtet ist, als oberster Bestandteil einer dekorativen Laminatanordnung und

    (c) Hitze- und Druckverbindung der Anordnung, wodurch die Partikel innerhalb der äußersten 25 um der Dicke des resultierenden Laminates angeordnet sind.


     


    Revendications

    1. Stratifié décoratif, consolidé par chauffage et sous pression, comprenant, en superposition,

    (a) un substrat autoporteur,

    (b) une feuille décorative imprégnée de résine thermodurcie, et

    (c) une feuille facultative de recouvrement imprégnée de résine thermodurcie,


    la surface extérieure dudit stratifié contenant des particules minérales,
    caractérisé en ce que lesdites particules possèdent une durété Mohs d'au moins 5, un diamètre compris dans l'intervalle de 5 à 100 nm et sont placées dans les 25 um les plus externes de l'épaisseur dudit stratifié et en une quantité comprise dans l'intervalle de 0,5 à 25 g/m2 de surface du stratifié.
     
    2. Stratifié décoratif suivant la revendication 1, dans lequel la substance minérale est la silice.
     
    3. Stratifié décoratif suivant la revendication 1, dans lequel le diamètre des particles de la substance minérale est compris dans l'intervalle de 20 à 60 nm.
     
    4. Stratifié décoratif suivant la revendication 1, dans lequel les particules minérales sont présentes dans les 15 pm les plus externes de l'épaisseur du stratifié.
     
    5. Stratifiée décoratif suivant la revendication 1, dans lequel la quantité de particules minérales présente dans la surface dudit stratifié est comprise dans l'intervalle de 1 à 10 grammes par mètre carré de surface du stratifié.
     
    6. Procédé de préparation d'un stratifié décoratif suivant l'une quelconque des revendications 1 à 5, qui consiste:

    a) à former une feuille constitutive imprégnée de résine thermodurcissable contenant des particules minérales, suivant la revendication 1,

    b) à mettre en place ladite feuille constitutive, sa surface portant les particules étant tournée vers le haut, afin de servir de constituant supérieur d'un assemblage de stratifié décoratif, et

    c) à consolider par chauffage et sous pression ledit assemblage, lesdites particules étant ainsi placées à l'intérieur des 25 pm les plus externes de l'épaisseur du stratifié résultant.