Composition for coating

Abstract

The method consists of the formation of a layer over a stone substrate to increase its hardness, chemical resistance, wear and scratch resistance, comprising applying on the substrate a coating matrix incorporating an organic material and fillers including inorganic nanoparticles and/or microparticles; chemically binding said matrix to the substrate, by a self-assembly process and/or a binding process by covalent bonding, electrostatic bonding, van der Waals bonding or hydrogen bonds; and finally drying said matrix. The mentioned organic material is selected from organosilanes, organophosphates, polycarboxylic compounds, compounds based on triazine heterocycles and said nanoparticles are nanoparticles of oxides, carbides, borides, nitrides of metals or of semimetals.

Claims

1. A method for coating a stone substrate based on a mixture of stone aggregates with materials selected from the group consisting of calcareous materials and dolomitic limestones that are agglomerated by means of a binder, the method comprising: forming a coating layer over the stone substrate to increase hardness, chemical resistance, wear and scratch resistance, said forming of the coating layer comprising the steps of: activating a surface of said stone substrate by means of selection from an oxidation of the surface and a chemical functionalization process, providing thereby active sites on the surface of the substrate; said sites having functional groups; applying on said activated stone substrate a coating matrix incorporating at least one organic material selected from the group consisting of organosilanes, organophosphonates, polycarboxylic compounds and compounds based on triazine heterocycles, and further incorporating fillers selected from the group consisting of inorganic nanoparticles and inorganic microparticles; chemically binding said coating matrix to the activated stone substrate by conducting a self-assembly process with the functional groups and a binding process selected from the group consisting of covalent bonding, electrostatic bonding, van der Waals bonding and hydrogen bonding, and any combination thereof; and drying said coating matrix, selecting the functional groups each from the group consisting of SI—OH, SiOR (R=organic compound), Si—CI, aldehyde, ketone, COOH, NH.sub.2 phosphates, phosphonates, sulfonates, sulfates and any combination thereof; selecting said inorganic nanoparticles and said inorganic microparticles from the group consisting of alumina, boron carbide, boron nitride, silicates, glass microspheres, silicon carbide, silica, quartz, copper oxide, micro- and nanofibers, core-shell particles, Na.sub.2SiO.sub.3 and any combination thereof; and wherein said chemically binding causes formation on the surface of the stone substrate a three-dimensional lattice by means of an interaction of the at least one organic material both with the surface of the substrate and between components of the coating matrix, wherein said three-dimensional lattice is bound to the surface of the activated stone substrate by chemical bonds and is encapsulating said nanoparticles and/or microparticles while maintaining an appearance of an original piece.

2. The method according to claim 1, wherein said coating matrix further comprises an organic or inorganic binder, an aqueous alcoholic or hydroalcoholic solvent and a cross-linking reaction accelerator.

3. The method according to claim 1, wherein said drying of the coating matrix comprises a step of applying heat to the coated substrate to accelerate a dehydration process of said functional groups and promote cross-linking thereof.

4. A method for coating a stone substrate, which is based on a mixture of stone aggregates with materials selected from the group consisting of calcareous materials and dolomitic limestones that are agglomerated by means of a binder, the method comprising: activating a surface of said stone substrate by means of selection from an oxidation of the surface and a chemical functionalization process, providing thereby active sites on the surface of the substrate applying bi- or multifunctional organic molecules in the form of a hydroalcoholic-based solution of organosilanes on the activated surface of the stone substrate; co-depositing inorganic microparticles and inorganic nanoparticles on the activated surface of the stone substrate to chemically bind the bi- or multifunctional organic molecules to the inorganic microparticles and inorganic nanoparticles to constitute a coating matrix; heat treating the hydroalcoholic-based solution of organosilanes to give rise to dehydration of silanol units, which change from Si—OH to Si—O—Si groups to allow a cross-linking between the surface of the stone substrate and the coating matrix; providing self-assembly from formation of covalent bonds and interactions between functional groups of the activated surface of the stone substrate and functional groups of the bi- or multifunctional organic molecules of the coating matrix to form a self-assembled, three-dimensional lattice in which is trapped and encapsulated the inorganic microparticles and the inorganic nanoparticles.

5. The method of claim 4, further comprising: selecting functional groups of the bi- or multifunctional organic molecules from the group consisting of: Si—O—R (R=organic compound), Si—Cl, aldehyde, ketone, CO, COOH, phosphates, sulfates, and any combination thereof.

6. The method of claim 4, wherein the coating matrix is formed from a dispersion of the inorganic nanoparticles or the inorganic microparticles or a combination thereof, the inorganic nanoparticles or the inorganic microparticles being in an aqueous solvent that allows a surface hardness of the stone substrate to increase by more than 2 points of a Mohs scale, the aqueous solvent being selected from the group consisting of an alcoholic aqueous solvent and a hydroalcoholic aqueous solvent.

7. The method of claim 4, wherein the interactions are selected from the group consisting of electrostatic interactions and van der Waals interactions.

8. A method for coating a stone substrate based on a mixture of stone aggregates with materials selected from the group consisting of calcareous materials and dolomitic limestones that are agglomerated by means of a binder, the method comprising: activating the surface of the stone substrate by means of selection from an oxidation of the surface and a chemical functionalization process, providing thereby aldehyde or hydroxyl functional groups on the surface of the stone substrate, effecting a reaction of the aldehyde or hydroxyl functional groups with amine functional groups of bi- or multifunctional organic molecules, the amine functional groups having at least three amino groups and co-depositing inorganic microparticles and inorganic nanoparticles on the surface of the activated stone substrate to chemically bind the bi- or multifunctional organic molecules to the inorganic microparticles and inorganic nanoparticles; providing self-assembly by the bi- or multifunctional organic molecules and the activated surface of the stone substrate from reaction of the aldehyde or hydroxyl functional groups with the amine functional groups to form a self-assembled, three-dimensional lattice in which said inorganic microparticles and inorganic nanoparticles are trapped and encapsulated.

9. The method of claim 8, wherein self-assembly is from formation of covalent bonds and interactions between the amine functional groups of the bi- or multifunctional organic molecules, further comprising: selecting the interactions from the group consisting of electrostatic interactions and van der Waals interactions.

10. The method of claim 8, wherein the self-assembly process is carried out with the at least three amino groups selected from the group consisting of melamine, triamines, and tetraamines.

11. A method for coating a stone substrate based on a mixture of stone aggregates with materials selected from the group consisting of calcareous materials and dolomitic limestones that are agglomerated by means of a binder, the method comprising giving rise to the coating by: activating a surface of the stone substrate to create functional groups on the surface of the stone substrate with carboxyl and hydroxyl groups by means of selection from an oxidation of the surface and a chemical functionalization process, providing thereby carboxyl and hydroxyl functional groups on the surface of the stone substrate; applying bi- or multifunctional organic molecules that have functional groups, and co-depositing inorganic microparticles and inorganic nanoparticles on the activated surface of the stone substrate to which the bi- or multifunctional organic molecules bond by chemical adsorption; and providing self-assembly from formation of covalent bonds and interactions between the functional groups on the surface of the activated surface of the stone substrate and the functional groups of the bi- or multifunctional organic molecules to form a self-assembled, three-dimensional lattice in which the inorganic microparticles and the inorganic nanoparticles are trapped and encapsulated.

12. The method of claim 11, wherein the functional groups of the bi- or multifunctional organic molecules are selected from the group consisting of: Si—O—R (R=organic compound), Si—Cl, aldehyde, ketone, CO, COOH, phosphates, sulfates, and any combination thereof.

13. The method of claim 11, wherein said inorganic nanoparticles or inorganic microparticles are co-deposited in a form of a dispersion in an aqueous solvent that allows a surface hardness of the stone substrate to increase by more than 2 points of a Mohs scale, the aqueous solvent being selected from the group consisting of an alcoholic aqueous solvent and a hydroalcoholic aqueous solvent.

14. The method of claim 11, wherein the coating is formed by a molecular anchoring process that effects the chemical binding.

15. The method of claim 14, further comprising: selecting the chemical binding from the group consisting of covalent bonding, electrostatic bonding, van der Waals bonding, hydrogen bonding and chemical adsorption, and any combination thereof.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) In said drawings:

(2) FIG. 1 schematically shows the self-assembly process on the substrate, this layer is formed from a hydroalcoholic organosilane solution. The cross-linking due to the dehydration of SiOH . . . HOSi units and which give rise to Si—O—Si bonds, occurs after a heat treatment at low temperatures;

(3) FIG. 2 shows a nanoparticle the structure of which is formed by 2 units, a core of a composition and an outer part of a different composition; an onion type nanoparticle;

(4) FIG. 3 shows a thin self-assembled layer on the surface of the substrate in which octanuclear Si.sub.4O.sub.4 units are shown;

(5) FIG. 4 shows other example of functionalization of surfaces and self-assembly based on the use of amino and aldehyde functional groups.

(6) FIG. 5 shows an example in which molecules with aldehyde functional groups and triazines for the self-assembly process are used. The incorporation of triazines allows creating three-dimensional lattices.

(7) FIG. 6 schematically shows a self-assembly process on a substrate according to the principles of this invention: mild oxidation of the surface, self-assembly and deposition of the nanocomposite. This process can occur in 3 steps, in two steps and even in a single step.

(8) FIG. 7 shows the incorporation of silanols in the matrix due to a spontaneous self-assembly. In this process the dehydration and formation of the bond occurs.

(9) FIG. 8 shows in its top part a coating structure according to the invention with microparticles only, whereas in the bottom part a structure in which microparticles and nanoparticles are combined is depicted.

DETAILED DESCRIPTION OF SEVERAL EMBODIMENTS

(10) The invention provides a coating with high hardness based on nanofillers and/or microfillers together with a TEOS, silane bond matrix etc.

(11) The invention proposes the formulation of a hard coating based on the dispersion of said nanofillers and/or microfillers in an alcoholic or hydroalcoholic aqueous solvent which allows increasing the surface hardness of a stone substrate by more than 2 or 3 points in the Mohs scale.

(12) Said development consists of a matrix of multifunctional molecules wherein one of the functional groups is capable of self-assembling or covalently bonding, thus being molecules with at least one of the following groups: Si—O (R=organic compound) or Si—Cl, aldehyde or ketone, CO or COOH, phosphates, sulfates, or the combination of one of these groups such as thiolphosphonate, which will produce a three-dimensional lattice due to a spontaneous self-assembly. Some of the used molecules are: thiols, alkoxysilanes, carboxylic acids, alkoxymetallates and phosphonic acids.

(13) The second functional group is a group capable of initiating the polymerization of monomers in a controlled manner.

(14) Some of the functional molecules used are: Tetraethyl orthosilicate, bis-1,2 (triethoxysilyl)ethane, 3-glycidoxypropyltrimethoxysilane, gamma-aminopropylsilane, dichlorodimethylsilane, bis-dichloromethylphenylsilane, and hexadecyltrimethoxysilane.

(15) To favor the adhesion with the substrate of the fillers, the aqueous/hydroalcoholic medium can be acidified by means of adding acetic, hydrochloric, tartaric, ethylenediaminetetraacetic, etc., type acid which favor the self-assembly by means of creating silanol, carboxyl or phosphonate groups.

(16) The micro and nanoparticles finally selected are stable in aqueous medium and/or colloidal solution and are added during the oligomerization of the developed molecule, thus allowing a good control of the percentage of nanofillers with additives.

(17) The choice of the used fillers was made based on the composition, structure, size and cost thereof. Some of the fillers considered are: Alumina (Al.sub.2O.sub.3) Boron carbide (B.sub.4C) Boron nitride (BN) Silicates Glass microspheres Silicon carbide (SiC) Silica (SiO.sub.2) Quartz Copper oxide (CuO) Micro- and nanofibers

(18) To promote the molecular cross-linking between the surface of the stone substrate and the multifunctional nanostructured coating, a self-assembly (SAM) technology is used which allows creating strong bonds disregarding the polarity of the surfaces to be bound, furthermore maintaining the appearance of the original piece.

(19) The self-assembly technology is based on the fact that the surface of some materials can be modified through a surface activation, which could consist of a moderate oxidation thereof, and/or of a chemical functionalization process using molecules capable of self-assembling.

(20) This new technique provides an effective bond between the surface of the material and the coating of micro- and nanoparticles, due to the possibility of forming a molecular cross-linking in the surface while the appearance of the original piece is maintained.

(21) This molecular anchoring process involves three steps: activation, self-assembly and co-deposition of micro- and nanoparticles. These three steps can be performed in a single step: activation, self-assembly and co-deposition of micro- and nanoparticles as is detailed in FIG. 6, when the molecules responsible for the activation and for creating three-dimensional lattices on the surface of the substrate and the micro- and nanofillers are in the same composition.

(22) The first step involves an activation in moderate conditions of the surface of the substrate to be treated for the purpose of functionalizing it, creating optimal functional groups for the self-assembly of organic molecules in the surface thereof, for increasing the potentiality of said surface to give rise to self-assembly reactions.

(23) The carboxyl and hydroxyl groups formed during the activation process (first step) provide the active sites so that the molecules are self-assembled with the suitable functional groups (second step). In said second step the self-assembly technique based on the formation of covalent bonds and other weaker interactions such as electrostatic or van der Waals interactions between the functional groups of the surface of the activated substrate and bi- or multifunctional organic molecules is applied. Thus, stable molecules chemically bound to the surface of the piece must be spontaneously produced.

(24) In the third step, the co-deposition of inorganic micro- and nanoparticles with high hardness (SiC, BN, SiO.sub.2, TiO.sub.2, ZrO.sub.2, quartz, alumina, B.sub.4C, etc . . . ) occurs on the surface of the substrate to obtain a high quality coating. The micro- and/or nanoparticles are trapped in the lattice which said molecules are capable of forming, maximizing the matrix-particle interaction. The self-assembled molecules are bound to the surface by means of a chemical adsorption process (the binding of the adsorbate to the solid surface by forces where their energy levels are close to those of the chemical bonds) providing an effective binding between the substrate and the molecules.

(25) These three phases can be reduced to a single one, to that end it is necessary to use in the same formulation the hard micro- and nanoparticles of the third phase and which will be co-deposited in the coating together with the molecules capable of functionalizing the surface of the substrate and creating three-dimensional lattices by means of self-assembly.

(26) A hard, transparent coating is obtained with a binding by means of chemical or electrostatic interactions or bonds, which have a high abrasion resistance, maintaining mechanical properties.

(27) Using this technology, from organic and inorganic precursors with the ability to form a three-dimensional lattice, different micro- and/or nanoparticles are encapsulated.

(28) The incorporation in the matrix of multifunctional molecules with at least one of the following groups: Si—O or Si—Cl, CO or COOH, amine, carbonyl, free aldehyde groups, carboxyl, phosphates, sulfates, or the combination of one of these groups such as thiolphosphonate produces a three-dimensional lattice due to a spontaneous self-assembly as is shown in FIG. 7 (for the case of silanol groups).

(29) With reference to the figures of the drawings, it must be emphasized that when the marble surface, formed mainly from crystalline structures of metal carbonates, the major one being calcium carbonate, is treated with compounds such as organosilanes, phosphonates, thiols, compounds with amino, aldehydes or carboxyl groups, a deposition of thin layers occurs on the XCO.sub.3 units, giving rise to —O—X—O—Si type bonds, for the case of organosilanes.

(30) For this type of material, silicon compounds form Si—O—Si—O type bonds, thus forming three-dimensional structures with excellent adherence to the marble substrate.

(31) If a hydroalcoholic-based solution of organosilanes is heat-treated at low temperatures, it gives rise to a dehydration of the silanol units which change from Si—OH to Si—O—Si type groups (with or without an organic chain), allowing a cross-linking between layers (FIG. 1).

(32) According to the silane molecule used (BTSE; TEOS, GLYMO, etc . . . ), the structure of the nanoparticle can be formed by octanuclear units (SiO).sub.4 (FIG. 3), onion type (FIG. 2), etc . . . These silicon oxide (SiO) nanoparticles created “in situ” are deposited on the surface of the substrate and, by means of a self-assembly process, are chemically bound to the surface. Anther example of functionalization of surfaces and self-assembly is the reaction between bi- or multifunctional aldehydes and surfaces chemically modified with amine groups. In this case, reactions of self-assembly will occur between the amine functional groups and the aldehyde groups (FIG. 4). When molecules with aldehyde functional groups are used to give self-assembly reactions, different types of agents can be used which allow creating three-dimensional lattices by means of reaction with free aldehyde or hydroxyl groups. These molecules must have at least 3 free amino groups as for example melamine, tri- or tetraamines, etc. (FIG. 5).

(33) Micro- and/or nanoparticles with a high hardness will be incorporated to the formulation to increase the hardness and wear resistance of the coating even more. Some nanostructured coatings are approximately three times more resistant than the coatings commonly used and last 40% more. With this method the nanoparticles can be directly applied to the surface of the coating and the final cost can be significantly reduced. Furthermore, the possibility of achieving a customized thickness from a nanolayer to microns contributes to a cost reduction.

(34) The developed product consists of a novel coating with thicknesses between 100 nanometers and 500 microns formed by the co-deposition by means of the self-assembly of micro- and nanoparticles with high hardness, using to that end an organic or organometallic matrix with the capacity to give self-assembly reactions both on the surface of the substrate and between the components of the formulation, allowing the formation of three-dimensional lattices.

(35) Until the optimal formulation of the coating was achieved, different types of functional molecules, solvents, as well as fillers varied in chemical composition, structural composition as well as particle size were tested.

(36) The application parameters (layer thickness, drying temperatures, . . . ), treatment forms (immersion, gun spraying, . . . ), etc . . . also influence the qualitative result and final behavior of the coating.

(37) All these factors affect the hydrophobicity of the coating, the surface tension generated, the correct cross-linking of the molecules, the more or less transparent appearance, bubble generation, the loss of adhesion causing for example afterwards a sticky surface, cracking, etc . . .

(38) Therefore, the right combination of the correct binding agents, the activation of the suitable solvent medium, the optimal fillers, as well as the application method and some specific application parameters, finally lead to obtaining an effective and chemically stable coating.

(39) Several Examples of implementation of the invention are detailed below by way of a non-limiting illustration.

EXAMPLE 1

(40) 1 ml of hydrochloric acid is added to a magnetically stirred ethanol/water (80 ml ethanol; 20 ml H.sub.2O) hydroalcoholic solution. 55 ml of TEOS (tetraethyl orthosilicate) and 23 ml of GLYMO (3-glycidoxypropyltrimethoxysilane) are added. The solution is left stirring for 10 minutes and 5.4 g of alpha-silicon carbide with a particle size of 80 nm are added. The mixture is left stirring for 5 minutes and is applied on the surface of the artificial marble slabs.

(41) It is left to dry in an oven at 120° C. for 25 minutes.

EXAMPLE 2

(42) 1 ml of hydrochloric acid is added to a magnetically stirred ethanol/water (80 ml ethanol; 20 ml H.sub.2O) hydroalcoholic solution. 40 ml of TEOS (tetraethyl orthosilicate) and 40 ml of GLYMO (3-glycidoxypropyltrimethoxysilane) are added. The solution is left stirring for 10 minutes and 5.4 g of alpha-silicon carbide with a particle size of 1 micron are added. The mixture is left stirring for 5 minutes and is applied on the surface of the artificial marble slabs.

(43) It is left to dry in an oven at 85° C. for 45 minutes

EXAMPLE 3

(44) The artificial marble slab (substrate) is introduced in an aqueous solution of HCl at 3.5% by volume for 40 seconds at 25° C. The substrate is washed with water 3 times and the substrate is left to dry.

(45) 1 ml of hydrochloric acid is added to a magnetically stirred ethanol/water (80 ml ethanol; 20 ml H.sub.2O) hydroalcoholic solution. 25 ml of TEOS (tetraethyl orthosilicate) and 55 ml of GLYMO (3-glycidoxypropyltrimethoxysilane) are added. The solution is left stirring for 10 minutes and 4.4 g of alpha-silicon carbide with a particle size of 1 micron and 1 g of alpha-silicon carbide with a particle size of 80 nm are added. The mixture is left stirring for 5 minutes and is applied on the substrate.

(46) It is left to dry in an oven at 85° C. for 45 minutes

EXAMPLE 4

(47) The artificial marble slab (substrate) is introduced in an aqueous solution of HCl at 3.5% by volume for 40 seconds at 25° C. The substrate is washed with water 3 times and the substrate is left to dry.

(48) 1 ml of hydrochloric acid is added to a magnetically stirred ethanol/water (80 ml ethanol; 20 ml H.sub.2O) hydroalcoholic solution. 55 ml of TEOS (tetraethyl orthosilicate) and 25 ml of GLYMO (3-glycidoxypropyltrimethoxysilane) are added. The solution is left stirring for 10 minutes and 25 g of silica with a particle size of 6 microns are added. The mixture is left stirring for 5 minutes and is applied on the substrate.

(49) It is left to dry in an oven at 85° C. for 45 minutes

(50) By combining the new hard coating based on micro- and/or nanofillers and a formulated silane (or phosphonates) bond matrix and this binding technique with the substrate: A stable coating on the substrate has been achieved. Increasing the hardness of the substrate has been achieved. Improving the scratch resistance of the substrate has been achieved. The adherence of the coating to the substrate has been improved since a chemical bond between the coating and the polyester resin has been created. The chemical resistance and resistance to detergents of the test pieces have been improved. Working at low temperature has been achieved. Work is carried out in a medium with low toxicity since the solvent used is an aqueous or hydroalcoholic medium, thus preventing harmful volatile emissions and without risk of irritation or other health risks for the person handling the solution.

EXAMPLE 5

Etching Test

(51) Some marble pieces are polished and an etching and staining test is subsequently performed therein comparing with non-polished pieces. The result is that the polished pieces have been out of coating and are easily attacked by the hydrochloric acid.

(52) The areas where it is observed that there is coating remain without alteration. In this case, the achieved hardness reaches 6 in the Mohs scale compared to 3 of the untreated piece. A certain splitting is seen but no scratch is observed nor does loss of material occur.

(53) When hydrochloric acid and lye are poured, bubbling does not occur and no reaction occurs until several hours have elapsed. In contrast, an untreated piece is etched straightaway and the marble is immediately consumed.

(54) The method of the invention allows achieving the following specific objectives: Improvement of the behavior against abrasion without altering the original appearance of the substrate. It does not affect other properties of the end product (bending, impact resistance, processability, physical characteristics, mechanical properties, etc.) With this new treatment, a stable coating is formed which is long-lasting, mainly due to the high adherence on the substrate which is generated by means of the formation of robust interactions of electrostatic, covalent type, etc., between the coating and the substrate. It works in a broad range of stone substrates based on a mixture of stone aggregates agglomerated by means of an organic binder. The binder used as a binding agent of the stone material being able to be both thermosetting and thermoplastic. The nature of the mineral varies according to the petrographic origin of the chosen natural stone (marble, limestone, quartz, granite, etc . . .) It prevents agglomeration problems when working in bulk. It reduces the generation of waste after the production process: decrease of the rejection of scratched pieces. The additional costs of the end product are minimum. There are no environmental risks or health risks since they are treatments based on volatile-free solvents. Upon working at low temperature it is possible to have pieces without apparent degradation, unlike what can occur with more aggressive deposition systems such as those of plasma or corona.