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    • 专利摘要:
    COATING COMPOSITION, METHOD OF FORMATION OF A COATING COMPOSITION, USE OF A COATING COMPOSITION, COATED SUBSTRATE, AND, METHOD OF FORMATION OF A COATED SUBSTRATE. A coating composition comprising an aqueous dispersion of submicron particles of natural ground calcium carbonate contained in a liquid binder, wherein the resulting coating may constitute either a clear coating or a glossy or opacifying coating, depending on the presence of certain additives such as a mineral pigment (eg TiO2). The composition is characterized by the fact that it comprises, in the case of a clear coating, at least one natural calcium carbonate with an average diameter between 0.05 and 0.15, (Mi) m while in the case of a glossy coating and opacifier, at least one ground natural calcium carbonate with an average diameter comprised between 0.05 and 0.3 (Mi)m and at least one pigment having a refractive index greater than or equal to 2.5.
    公开号:BR112013021170B1
    申请号:R112013021170-9
    申请日:2012-02-23
    公开日:2021-05-25
    发明作者:Joseph McJunkins；Charles Freeman
    申请人:Omya International Ag；
    IPC主号:
    专利说明:

    technical field
    [0001] The present invention relates to coating compositions comprising submicron particles comprising ground natural calcium carbonate (hereinafter SMGCC). The invention further relates to a process for preparing coating compositions containing SMGCC, and the use of SMGCC in coating compositions. The coating composition(s), depending on their composition, can be used to form the clear coatings. Brief Description of Drawings
    [0002] Figures 1A and IB are microphotographs of Omya XC-6600-34 CaCO3, and
    [0003] Figure 2 is a series of particle size distribution curves that contain the data for a series of samples, whose D98 value is <0.3 μm. The values for D90, D50 and D20 for these samples can be determined by comparing the x and y axis. Background and Detailed Description
    [0004] The aqueous dispersion of nanoparticles of the present invention can be used to make coatings and films for porous and non-porous substrates, such as papers, non-woven materials, textiles, leather, wood, concrete, masonry, metals, house wrap and other building materials, fiberglass, polymeric articles, personal protective equipment (such as hazardous material protective clothing, including face masks, curtains and medical apparel, and firefighter engagement equipment) and the like. Applications include papers and non-woven materials, fibrous materials, films, sheets, composites and other articles, industrial and decorative paints and coatings, flakes and other adhesives, and personal care products such as skin care, hair care and care nails, livestock and seed applications, and the like.
    [0005] Any fibrous material can be coated, impregnated or otherwise treated with the compositions according to the invention by methods well known to those skilled in the art, including carpets, as well as textile products used in clothing, upholstery, awnings, tents, airbags and the like. Suitable textiles include fabrics, yarns and blends, whether woven, non-woven or knitted and naturally occurring, synthetic or regenerated. Examples of suitable textiles include cellulose acetate, acrylic, wool, cotton, jute, linen, polyesters, polyamides, regenerated cellulose (i.e., viscose) and the like.
    [0006] The compositions, depending on their intended application, can be dispersed in a variety of binders, including, but not limited to, vinyl-acrylics, styrene-acrylics, acrylic dispersions, acrylic solutions, alkyd resins (eg, SOYA , TOFA, sunflower, etc.), polyurethanes dispersed in water or solvent, etc., hereinafter referred to as "binding medium".
    [0007] Furthermore, the compositions according to the invention can be used as adhesives or to augment or complement types of adhesives well known to those skilled in the art. Thus, in the application discussed above, where the compositions are used as adhesives or to augment or complement various types of known adhesives, particularly desirable properties can be obtained by varying the type and amount of aqueous nanoparticles used, along with choosing a complementary binding means of one or more of those listed above, or by incorporating other binding materials that would be well known to those skilled in the art.
    [0008] As noted above, coatings containing the compositions according to the invention can be formulated as substantially clear coatings, i.e. generally referred to as "clear coatings". Clear coating composites produced when aqueous dispersions are applied and dried, exhibit excellent gloss and clarity. Furthermore, provided the D98 particle size of the substantially dispersed nanoparticles contained in the coating composition is <350 nm, preferably <300 nm and the D50 is <200 nm, preferably <150 nm, the coatings obtained will be essentially transparent, provided it is clear that they are free or essentially free from additional components that could comprise their transparency properties.
    [0009] One aspect of the invention relates to a clear coating composition according to claim 1.
    [0010] Another aspect relates to a method of forming a clearcoat composition according to claim 7.
    [0011] A further aspect relates to the uses of clear coating compositions according to the invention for coated substrates.
    [0012] Another aspect relates to substrates coated with a clear coating composition according to the invention.
    [0013] Yet another aspect relates to a method of forming a coated substrate with a clear coating composition according to the invention.
    [0014] For exemplary and non-limiting purposes of the invention, a useful medium for the binder, for example clear coatings according to the invention are polymers containing ester groups such as, for example, polyesters, polyurethanes based on polyester, polyester-based polyureas and polyester-based polyamides. These various binders, however, have less than desirable water resistance properties due to the hydrolysis group contained therein.
    [0015] It has been determined, on the other hand, that the water resistance properties of such polyester-based polyurethanes can be remarkably increased, without affecting the transparency properties of these materials to any significant degree, by combining with a polymer binder, a proton scavenger of substantially dispersed nanoparticles, such as particles comprising ground natural calcium carbonate. The resulting coating composition, therefore, which in turn is only described to exemplify (and not limit) the invention, therefore constitutes a hydrolytically stable polyurethane nanocomposite comprising a solid polyester-polyurethane polymer binder containing nanoparticles of proton scavengers in a substantially dispersed form. A specific useful example of such a formulation is a colloidally stable aqueous dispersion comprising water, a polyester-polyurethane polymeric binder and substantially dispersed proton scavenger nanoparticles such as SMGCC.
    [0016] In the sense of the present invention, the term "substantially dispersed" means that the nanoparticles are suitably dispersed in an aqueous medium in order to avoid sedimentation or syneresis of the nanoparticles. This is generally achieved through the addition of well known dispersing agents which comprise homo- or copolymer chains. If necessary, the chains can be partially or fully neutralized by cations such as sodium, lithium, magnesium, calcium, potassium or ammonium.
    [0017] Coatings with the composition of the exemplary formulation described above therefore constitute the polyurethane compositions which, for example, have improved hydrolytic stability over prior art polyurethane compositions. As used herein the term polyurethane is used generically to describe polymers including oligomers (eg, prepolymers) that contain the urethane group, i.e., -O-C(=O)-NH-, regardless of how they are made. As is well known, these polyurethanes may contain additional groups such as urea, allophanate, biuret, carbodiimide, oxazolidinyl, isocyanurate, uretdione, alcohol, amine, hydrazide, siloxane, silane, ketone, olefins, etc., in addition to the urethane groups.
    [0018] The present invention includes, as described herein, the use of substantially dispersed nanoparticles (referring to primary crystallites or particles of a proton scavenger and or proton scavenger aggregates) of proton scavenger nanoparticles to increase the water resistance (hydrolytic stability) of thermoplastic polyurethanes containing polyester segments within the polyurethane polymer or prepolymer. Thermoplastic polyurethanes are made with the same components as polyester polyurethanes by water (polyurethane dispersions in water), immediately below, but typically thermoplastic polyurethanes have substantially less or no compound(s) with improved water dispersibility. In one embodiment, the hydrolytically stable polyurethane is a thermoplastic polyurethane. Technology for the manufacture and use of thermoplastic polyurethanes is well known and described, for example, in US 6,777,466 B2 and J. Backus ET AL., "Polyurethanes", in: Encyclopedia of Polymer Science and Engineering. Vol. 13, H.F. Mark et al., Ed., pp 243-303 (1988), the entire disclosure of which is incorporated herein by reference.
    [0019] Furthermore, the invention in one embodiment relates to polyester polyurethanes which are derived from aqueous dispersions and which, when dried and cured, produce solid polyester segment containing polyurethane products, which are hard and depending of the other ingredients present (eg absence of TiO2 or other pigment), it may be a clear one.
    [0020] Further in accordance with this invention, it has been found that the susceptibility of polyester polyurethanes to degrade through hydrolysis can be essentially completely eliminated by incorporating into the polymer a substantially dispersed nano-particle proton scavenger (referring to if the aggregation and/or the final particles/crystallites).
    [0021] Certain materials are known to react with, bind to, or otherwise capture protons, ie, hydrogen ions, when exposed to the same, in solid, liquid and/or gaseous media. Calcium carbonate is a good example of what other alkali and alkaline earth metal carbonates are like, ie Li2CO3, BeCO3, MgCO3, SrCO3, BaCO3, and RaCO3. Other examples of proton scavenger carbonates include Fe(II), Fe(III), Mn(II), Zn, Ag, Hg(I), Hg(II), Cu(II), Pb(II), Bi carbonates (III).
    [0022] Calcium carbonate has the formula CaCO3. It is a common substance found in rock all over the world, and is a major component of the shells of marine organisms, snails, pearls, and eggshells. Calcium carbonate is found naturally as the following minerals and rocks: aragonite, calcite, vaterite or (μ-CaC03), chalk, limestone, marble, travertine. The vast majority of calcium carbonate used in industry is extracted by mining or quarrying. Pure calcium carbonate (eg for pharmaceutical or food use) can be produced from a pure extracted source (usually marble). Ground calcium carbonate (GCC) is produced by mechanically grinding naturally occurring calcium carbonate rocks: marble, limestone and chalk. GCC in pigment formulations provides good rheology and high gloss at low cost. Alternatively, raw calcium carbonate is calcined to calcium oxide (lime). Water is added to give calcium hydroxide, and carbon dioxide is passed through this solution to precipitate the desired calcium carbonate, known as precipitated calcium carbonate (PCC). This process produces very pure calcium carbonate crystals. Crystals can be adapted to a variety of different shapes and sizes depending on the specific reaction process used. The three main forms of PCC crystals are aragonite, rhombohedral and scalenohedral. Within each crystal type, the PCC process can control the average particle size, size distribution, and surface area. Precipitated calcium carbonate is used as a mineral pigment throughout the world for paper production. It is prized for its high gloss and light scattering characteristics in paper filling and coating applications.
    [0023] Other examples of inorganic compounds that scavenge protons include Ba, Ca, Mg, Al, Cr(III), Fe(II), Fe(III), Mn(II), Zn, Ag, Cu(II) silicates , Pb(II), Fe(II), Mn(II), Zn, Ag, Hg(I), Hg(II), Cu(II), Pb(II), Bi(III), Sn(II) sulfides ); oxides and hydroxides of the above metals, and hydroxyapatite, which is a naturally occurring mineral form of calcium apatite.
    [0024] Examples of organic compounds that scavenge protons include 1,8-bis(dimethylamino)naphthalene, 1,8-bis(hexamethyltriaminophosphazenyl)naphthalene and 2,6-di-tert-butylpyridine.
    [0025] Any combination of the above cleaners can be used.
    [0026] In accordance with the present invention, it has been found that this form of proton scavenging materials will substantially reduce or even completely eliminate the susceptibility of polyester polyurethanes to degrade through hydrolysis without introducing any significant haze into the polymer, but only if they are incorporated into the polymer in a substantially dispersed and/or high surface area nano-particle form.
    [0027] In this regard, nanoparticles are usually obtained commercially in powder or dispersion form, both aqueous and organic. Although the individual/primary particles (crystallites for CaCO3) in these products may be in the nano-size range, these particles generally combine into larger agglomerates, where the nanoparticles are relatively tightly-packed with each other typically in three dimensions. Therefore, when these nanoparticle powders and dispersions are used to make polymers containing nanoparticles, the nanoparticles remain in the form of these larger agglomerates. In other words, nanoparticles are not substantially dispersed in the polymer mass. In accordance with the present invention, it has been found that proton scavenger nanoparticles will substantially reduce or even completely eliminate the susceptibility of polyester polyurethanes to degrade through hydrolysis, but only if they are incorporated into the polymer mass ultimately formed in a substantially dispersed and/or high surface area form.
    [0028] An example of a substantially dispersed (but loosely aggregated) arrangement having a high surface area (eg 41 m2/g) is shown in figures 1A and 1B. The primary nanocrystallites of Omya OLC-6600-34 of Omya form flakes of various shapes and sizes with a substantial portion of the surface exposed to the matrix they are in. From this point of view, the most effective form of flocculation is a train or streams of particles. for nanocomposites, but it will still be effective in slowing down ester hydrolysis because most of the nanoparticle surfaces are exposed to the matrix.
    [0029] In one embodiment, when the final particle/crystallite diameter is small, desirably the D50 is less than 1 micron, more desirably less than 500 nm, more desirably less than 100 nm, and preferably less than 50 nm . In a similar embodiment, desirably the D90 is less than 1 micron, more desirably less than 500 nm, more desirably less than 100 nm, and preferably less than 50 nm. In one embodiment, the BET surface area of nitrogen is greater than 20 m2/g, more desirably greater than 30 m2/g, even more desirably greater than 35 m2/g, and preferably about 40 or more m2/g. g.
    In one embodiment, the particle size of the proton scavenger nanoparticles when in the substantially dispersed form desired for this invention can vary widely, and essentially any particle size in the nanoparticle size range can be used. For purposes of the present invention, substantially dispersed nanoparticles and nanoparticles are defined as those particles that have at least one of the three dimensions less than about 250 nm (D90), but typically will be less than about 150 nm. In other embodiments, the average particle size will be about 100 nm or less (D90), 75 nm or less, or even 50 nm or less. In some embodiments, the particle size can even be as low as 25 nm or less, 10 nm or less, or even 5 nm or less. In general, the average particle size, D50, of these substantially dispersed nanoparticles can be as large as 250 nm (nanometers), but will typically be less than 100 nm. Substantially dispersed nanoparticles with an average particle size of about 75 nm or less, more typically 50 nm or less, or even 40 nm or less are of interest. In other embodiments, the average particle size will be 30 nm or less, 25 nm or less, or even 10 nm or less. In some embodiments, the particle size can even be as low as 5 nm or less, 2 nm or less, or even 1 nm or less.
    [0031] Particle size is generally characterized by a particle size distribution, since all particles in a batch of particles do not have an identical particle size. Thus, in some embodiments of the invention, it is desirable that the batch of nanoparticles have a D90 of less than 250 nm (i.e. 90% of the volume of the particles in the batch have an equivalent diameter of less than 250 nm). Batches of nanoparticles with D90's of 150 nm or less, 100 nm or less, more typically 75 nm or less, or even 50 nm or less, 25 nm or less, 10 nm or less, or up to 5 nm or less, are especially interesting.
    [0032] Of particular interest are batches of nanoparticles containing D90's of about 100 nm or less, and in particular 75 nm or less, or even 50 nm or less, provided that nanoparticles of this size when substantially dispersed in a matrix of polymer become essentially transparent to the naked eye.
    [0033] The aqueous dispersions of nanoparticles/polyester-polyurethane, of the present invention, both in prepolymer and chain extended form, can be used to make coatings and films for porous and non-porous substrates, such as papers, materials nonwovens, textiles, leather, wood, concrete, masonry, metals, house wrap and other construction materials, fiberglass, polymeric articles, personal protective equipment (such as hazardous materials protective clothing including masks, medical curtains and dresses, and firefighter participation equipment), and so on. Applications include papers and nonwovens, fibrous materials, films, sheets, composites, and other articles, inks and printing pastes, flock and other adhesives, and personal care products such as skin care, hair, nail and hygiene products , livestock and seed applications, and the like.
    [0034] Any fibrous material can be coated, impregnated or otherwise treated with the compositions of the present invention by methods well known to those skilled in the art, including carpets, as well as textile products used in clothing, upholstery, awnings, tents, bags of clothing. air, and the like. Suitable textiles include fabrics, yarns and blends, whether woven, non-woven, or knitted, and naturally occurring, synthetic or regenerated. Examples of suitable textiles include cellulose acetate, acrylics, wool, cotton, jute, linen, polyesters, polyamides, regenerated cellulose (Viscose), and the like.
    [0035] The compositions of the present invention can also be used to produce articles made of independent films and objects such as personal protective equipment. Examples of protective items include gloves and condoms.
    [0036] Furthermore, the compositions of the present invention can be used as adhesives or to augment or complement types of adhesives well known to those skilled in the art. For example, certain adhesive properties can be achieved by varying the amount and type of isocyanates, type, amount, and molecular weight of polyols, and the amount of poly(alkylene oxide) side chain units.
    [0037] Polyurethane-polyurethane nanoparticle composites produced when the aqueous dispersions of the present invention are applied and dried, whether or not the polyester-polyurethane is chain extended, exhibit exceptional resistance to degradation by hydrolysis, in particular resistance to hydrolysis comparable to that of much more expensive polyurethane polycarbonate resins. Furthermore, while the D90 particle size of the substantially dispersed nanoparticles used is <75 nm, preferably <50 nm or even <40 nm, the polyurethanes obtained will be essentially transparent, provided, of course, that they are free or essentially free of others. materials that may compromise their transparency properties.
    [0038] Finally, the principles of the present invention can be applied to other technologies for the manufacture of aqueous polyurethane dispersions. For example, this invention can be applied with the technique for making breathable polyurethane dispersions (i.e. dispersions that form layers of breathable polyurethanes) described in US Patent No. 6,897,281, as well as the technique for making core-coat polyurethane dispersions described in US published patent application No. 20050004306. The above patent disclosures and published applications are hereby incorporated by reference.
    [0039] Polyurethanes based on polyester macroglycols are known to be susceptible to hydrolysis. The hydrolytic stability of the improved product is attributed to the presence of a proton scavenger in highly dispersed form having significant surface area (increasing the probability that the proton scavenger will be able to scavenge proton species before causing cleavage of the hydrolytic chain in the portion Polyurethane Polyester). Polyurethane can be in the form of a film, coating or molded article. The proton scavenger is preferably an inorganic carbonate salt such as calcium carbonate. If the proton scavenger aggregates are small relative to the wavelength of light the polyurethane composition will be substantially transparent to visible light. If the proton scavenger, eg calcium carbonate, is made up of loosely aggregated primary crystallites, which are weight average diameter 5-100 nanometers, which will have high surface area (eg >40 m2/g) , will be effective in eliminating protons.
    [0040] To further exemplify the clear coatings formulated according to the invention, some working examples of such clear coating formulations are provided below. In these examples, the following raw materials were used: • DOW - SG30 Acrylic Latex (binder medium) • Bayhydrol 110 - polyurethane dispersion (binder medium) • Deionized water • Various experimental Omya SM-CCG suspensions.
    [0041] In addition, the following analytical and testing procedures were used in carrying out these examples: • Brightness was measured at angles of 20°, 60° and 75° using a TriGloss Micro unit from BYK-Gardner, catalog No. 4446 • Sheen at 85° angle using a TriGloss Micro unit from BYK-Gardner, catalog No. 4446 • Solids Content - total solids were measured by Toledo HB 43 Unit/Solids Analyzer (Mettler Toledo Corporation) • pH measurements - pH readings pH values were made using pH Meter 510, a pH meter from BYK-Gardner, Catalog No. PH-2643. • Glow/Mist. The preferred haze assessment is visual because haze and perceived clarity are one of the most important properties of coatings and other articles. Fog can also be measured by objective instrumental means. Examples include the method described in ASTM D 1003-07 "Standard Test Method for Fog and Light Transmittance of Transparent Plastics", measuring brightness at different angles, measuring L, a, b values, and also other methods described in ASTM Guide El79-96 (2003) "Standard Guide for Selection of Geometric Conditions for the Measurement of Reflection and Transmission Properties of Materials", D1455 "Test Method for Specular Gloss at 60 Degrees of Polishing of Floor in Emulsion" , D1746 "Test Method for the Transparency of Plastic Sheets", D4039 "Test Method for Reflection Fog of High Gloss Surfaces", D4061 "Test Method for Retroreflection of Horizontal Coatings" and D523 "Test Method for Gloss Speculate". Preparation of a clear glossy coating containing calcium carbonate nanoparticles dispersion
    [0042] In each case, an aqueous dispersion of substantially dispersed calcium carbonate nanoparticles was produced from the following ingredients: Ingredients used in example 1

    Ingredients used in example 2
    Ingredients used in example 3
    Ingredients used in example 4
    Ingredients used in example 5
    Ingredients used in example 6
    Ingredients used in example 7
    Ingredients used in example 8

    Ingredients used in example 9
    Ingredients used in example 10
    Table 1 BRIGHTNESS MEASUREMENT

    [0043] Samples made with all Dow SG-30 acrylic latex were prepared using a Premier Mill Model #CM 100 high-speed dissolver with a 6.35 cm blade. They were dispersed for 30 minutes at 900 rpm. Ingredients used in example 11
    Ingredients used in example 12
    Ingredients used in example 13
    Ingredients used in example 14
    Ingredients used in example 15
    Ingredients used in example 16
    Ingredients used in example 17
    Ingredients used in example 18
    Ingredients used in example 19
    Ingredients used in example 20
    Table 2 Bayhydrol with 5% GCC loading
    Table 3 Bayhydrol with 10% GCC loading

    Samples made with Bayhydrol 110 were prepared using a Model # DAC 150.1 FVZ-K speed mixer. They were dispersed for 1 min at 2500 rpm.
    [0045] It is noted that mineral pigments are widely used in known glossy and opacifying coating systems, not only to further decrease formulation costs, but to improve certain properties of the coating formulation during its preparation or storage, or during or after its application to a substrate. In the realm of paint formulations, coating systems almost invariably add titanium dioxide.
    [0046] In the context of paint applications, titanium dioxide (TiO2) is commonly used, particularly in its rutile form, to provide significant opacity or hiding power. Titanium dioxide pigments marketed for use in paint formulations are well known to have a narrow particle size distribution along with an average particle diameter between 0.2 and 0.6 µm, depending on the material and method of measurement. of the average particle size. Zinc sulfide and zinc oxide are similarly employed.
    [0047] Titanium dioxide suffers, however from being relatively high cost, which results in a continuing desire to find lower cost TiO2 partial replacement pigments that will not translate into a reduction in the optical properties of the coating composition and others.
    [0048] GB 1404564 describes inks and pigments loaded with ultra-fine natural calcium carbonate, wherein said natural calcium carbonate has a particle diameter of 0.5 to 4 µm and is used to partially replace titanium dioxide. In this sense, Imerys has been marketing Polcarb, said to be suitable for concealing paint formulations, which has an average particle size of 0.9 µm. However, such natural calcium carbonate products do not allow the replacement of a portion of TiO2 in gloss paint formulation having a pigment volume concentration below the critical pigment volume concentration without loss of gloss and opacity.
    [0049] The pigment volume concentration (PVC) is understood to refer to the fraction, quoted in % of the pigment volume in relation to the total volume of the pigment plus the other components of the formulation, that is, which is responsible for the volume of pigment in relation to the total volume of the formulation.
    [0050] Critical pigment volume concentration (CPVC) is defined as the pigment volume concentration after which the resin component of the coating formulation is no longer fully sufficient to fully coat all pigment particles in a coating. It is well known that CPVC above formulations generally provide a matte finish. In contrast, gloss paint formulations implement a PVC that is below CPVC.
    [0051] US 5,171,631 discloses a coating composition for developing coverage on a suitable substrate, the coating composition having a pigment volume concentration (PVC), up to a critical pigment volume concentration (CPVC) and a system of pigment comprising about 70-98% by volume of titanium dioxide and about 2-30% by volume of an aluminum trihydrate (ATH) spacer/extender pigment with an average particle size of about 0. 2 microns. Figure 1 of US 5,171. 631 shows a D98/D50 ratio value of approximately 2.7, which corresponds to a relatively narrow particle size distribution. Although it is indicated that since this ATH has an average particle size and particle size distribution, generally similar to the average particle size and particle size distribution curve of TiO2, a portion of TiO2 can be replaced with an equal volume of ATH without loss of coverage, figure 2 of US 5,171,631 shows that ATH-TiO2 comprising paint formulations generally do not reach the same opacity values when the paint formulation control comprises TiO2 alone.
    [0052] Naturally ground calcium carbonate as opposed to its synthetic counterpart, precipitated calcium carbonate (PCC), in general, suffers from a wide particle size distribution and irregular particle shapes. Indeed, as ground natural calcium carbonate is prepared by grinding down mined calcite, marble, chalk or stones containing limestone, it is difficult to guarantee that these stones are finally fractionated to form fine particles with a very uniform particle size.
    [0053] In contrast, PCC is formed by a process of building crystals around nucleation sites. Control of nucleation and particle size development, particularly in the size domain under a few micrometers, during PCC precipitation, over the years, has become a well-studied science and PCC particles with very small and very small particle sizes and shapes uniforms are now widely available. As in US 5,171,631, the advantages of employing a uniform particle size product such as a titanium dioxide spacer are cited in the publication made at http://www.specialtyminerals.com/specialty-applications/specialty-markets- for-minerals/paint-and-coatings/precipitated-calcium-carbonate-pcc-in-paint/: "Precipitated calcium carbonate (PCC) is most commonly used in paint as a titanium dioxide extender, or TiO2. of small, closely distributed PCCs help to space the individual TiO2 particles and maximize their hiding power." In this domain, Specialty Minerals announces Albafil PCC, a fine, 0.7 micron prismatic calcite, and a range of ultra-fine or nano PCCs, namely Calofort S PCC, Calofort U PCC, Ultra-Pflex PCC and Multifex MM PCC, each one with an average diameter of 0.07 microns.
    [0054] In view of the above teachings found in the prior art, it was remarkable that the present inventors found that a ground natural calcium carbonate, which is finer than the ground calcium carbonate natural products previously proposed in this field, can be used to form an aqueous nanoparticle dispersion in one or more of the binder systems described above for use in forming a variety of (1) clear coating compositions (see discussion above) as well as those that serve as (2) a pigment substituting or complementing TiO2 in the formation of glossy and opacifying coating compositions, even in the case where ground natural calcium carbonate features a relatively broad particle size distribution and/or an average diameter that is different from that of TiO2. In contrast to the results of US 5,171,631 obtained with ATH, the ground natural calcium carbonate used in the present invention not only more completely maintains the gloss and opacity of the paint formulation when used to replace part of the TiO2 formulation with PVC constant, this can even lead to an improvement in brightness and/or opacity.
    [0055]The CPVC was determined according to the measurement method given in the examples section below.
    [0056] The mean diameter (d50 (Mal)) and D98 (Mal) were measured according to the measurement method given in the examples section below.
    [0057] The gloss of a coating composition applied to a substrate was measured according to the measurement method given in the examples section below.
    [0058] The opacity of a coating composition applied to a substrate was measured according to the measurement method provided in the examples section below.
    [0059] In order to more fully describe the formulation of the glossy and opacifying coating compositions, the following examples are provided below.
    [0060] The coating compositions according to the present invention (i.e. when used in forming clear coatings) can be applied to a variety of substrates as discussed above, including, but not limited to, concrete, wood, paper , metal and plate.
    [0061] In a preferred embodiment, the coating composition is applied to a substrate in an amount so as to form a layer having a thickness of between 100 and 400 µm.
    [0062] The present coating compositions may further include one or more of the following: optical brightener, resin (such as a latex or acrylate-based binder, preferably in the form of an aqueous emulsion), defoamer, thickener, solvent , glycol ethers and dispersant. Preferably, the coating composition has a Brookfield viscosity of 200 to 500 mPa.s, measured according to the measurement method given in the examples below. Examples of Gloss/Opacifying Coating Compositions Suspension or dispersion solids content (% equivalent dry weight)
    [0063] The weight of solid material in suspension or dispersion is determined by weighing the solid material obtained by evaporating the aqueous phase of the suspension and drying the material obtained at a constant weight. Particle size distribution (% by mass% of particles with a diameter <X) and mean grain diameter (D50 (Sedi), D50 (Mai) and D98 (Mai)) of particulate material
    [0064] Average grain diameter weight (D50 (Sedi)) and grain diameter mass distribution of a particulate material are determined through the sedimentation method, ie the analysis of the sedimentation behavior in a gravimetric field. The measurement is taken with a Sedigraph™ 5100.
    [0065] The method and apparatus are known to the skilled person and are commonly used to determine the grain size of fillers and pigments. The measurement is carried out in an aqueous solution of 0.1% by weight of Na4P2O7. The samples were dispersed using a high speed stirrer and ultrasonic medium.
    [0066] Average grain diameter weight (D50 (Mai)) was evaluated using a Malvern Mastersizer 2000 (Frauenhofer). The D98(Mai) value, measured using a Malvern Mastersizer 2000 (Frauenhofer), indicates a diameter value such that 98% by weight of the particles have a diameter less than this value. BET specific surface area (m2/g)
    [0067] The BET specific surface area values were determined using nitrogen and the BET method according to ISO 9277. Gloss of a coated surface
    [0068] Gloss values are measured at the listed angles according to DIN 67 530 on painted surfaces prepared with a coater range of 150 and 300 µm on contrast boards. Contrast ratio (opacity) of a coated surface
    [0069] Contrast ratio values are determined according to ISO 6504/3 at a propagation rate of 7.5 m2/l. Brookfield viscosity of the suspension or dispersion (mPas))
    [0070] Brookfield viscosities are measured with a Brookfield DV-II viscometer equipped with an LV-3 spindle at a speed of 100 rpm and room temperature (20 ± 3°C). Pigment volume concentration (PVC, %)
    [0071] The pigment volume concentration is calculated as described in Section 6.2.3 of the book titled "Fuellstoff" by Detlef Gysau (Hannover: Vincentz Network, 2005).
    [0072] Total sum in volume of all pigments + extenders in the paint / Total sum in volume of all solid ingredients in the paint x 100% Critical pigment volume concentration (CPVC, %)
    [0073] The critical volume concentration of the pigment is the well-known concentration widely used in the paint industry. It is generally considered to represent the point where there is just enough resin to wet the pigment particles, and changes to PVC close to CPVC can result in abrupt changes in coating properties, such as porosity and gloss. CPVC and the measurement method according to ISO 4618 are discussed in Section 6.2.4 of the book entitled "Fuellstoff by Detlef Gysau (Hannover: Vincentz Network, 2005). Materials: SMGCC
    [0074] SMGCC dispersions used in the following examples are calcium carbonate D50 and particle size characteristics given in the table below. Table 4
    Titanium dioxide
    [0075] The titanium dioxide used in the examples below consists of 95% by weight of pure rutile TiO2, with the remaining weight being accounted for in a surface treatment of alumina, zirconia and an organic surface treatment agent. This pigment has a d50 (Mal) of approximately 0.55 µm and is supplied as an aqueous paste having a solids content of 75%. Under the scanning electron microscope, the particles appear to be in the 0.2 to 0.25 µm range. The refractive index of TiO2 is 2.7. Example 21:
    [0076] The formulated inks were applied to a contrast plate in the necessary amounts in order to measure both gloss and opacity. Table 5

    [0077] The results presented in table 5 above demonstrate that replacing a portion of TiO2 with the SMGCC and having d98/d50 values ranging from 2.4 to 5, results in coatings that have essentially the same opacity (ratio of contrast) as the comparison formulation with equal PVC but only TiO2. Gloss values are found to be equivalent or improved over the comparison formulation having equal PVC but only TiO2.
    权利要求:
    Claims (19)
    [0001]
    1. Clear coating composition, characterized in that it comprises an aqueous dispersion of nanoparticles, where the nanoparticles are dispersed and have an average particle size D50 of less than 1 micron, where the nanoparticles are ground calcium carbonate and are dispersed in at least one binder including vinyl-acrylic, styrene-acrylic, acrylic dispersions, acrylic solutions, alkyds, polyurethanes dispersed in water or solvent, polymers containing ester groups including polyesters, polyester-based polyurethanes, polyester-based polyureas and polyamides Polyester-based.
    [0002]
    2. Clear coating composition according to claim 1, characterized in that the binder is a polyester-polyurethane polymer binder.
    [0003]
    3. Clear coating composition according to claim 1 or 2, characterized in that the nanoparticles have a D50 particle size of less than 500 nm, preferably less than 100 nm, and more preferably less than 50 nm.
    [0004]
    4. Clear coating composition according to any one of claims 1 to 3, characterized in that the nanoparticles have a D90 particle size of less than 1 micron, preferably less than 500 nm, preferably less than 100 nm, and more preferably less than 50 nm.
    [0005]
    5. Clear coating composition according to any one of claims 1 to 4, characterized in that the BET surface area of the nitrogen of the nanoparticles is greater than 20 m2/g, preferably greater than 30 m2/g, more preferably greater to 35 m2/g, and even more preferably 40 m2/g.
    [0006]
    6. Clear coating composition according to any one of claims 1 to 5, characterized by the fact that ground calcium carbonate is derived from grinding chalk, limestone, marble and is submicron ground calcium carbonate (SMGCC), in which the submicron ground calcium carbonate has an average diameter between 0.05 and 0.3 µm.
    [0007]
    7. Clear coating composition according to any one of claims 1 to 6, characterized in that the dispersed nanoparticles contained in the coating composition have a D98 particle size of <350 nm, preferably <300 nm, and a size of D50 particle of <200 nm, preferably <150 nm.
    [0008]
    8. Clear coating composition according to any one of claims 1 to 7, characterized in that it comprises a binder that includes vinyl-acrylic, styrene-acrylic, acrylic dispersions, acrylic solutions, alkyds, polyurethanes dispersed in water or solvent, polymers containing ester groups including polyesters, polyester based polyurethanes, polyester based polyureas and polyester based polyamides, the binder is preferably the polyester-polyurethane polymer binder containing submicron ground calcium carbonate which comprises particles in a dispersed form.
    [0009]
    9. Method of forming a clear coating composition as defined in any one of claims 1 to 8, characterized in that water, nanoparticles and at least one binder are combined and then dispersed to form the composition clear coating, wherein the binder includes vinyl-acrylic, styrene-acyclic, acrylic dispersions, acrylic solutions, alkyds, polyurethanes dispersed in water or solvent, polymers containing ester groups including polyesters, polyester-based polyurethanes, polyester-based polyureas and polyester-based polyamides.
    [0010]
    10. Method according to claim 9, characterized in that the binder is a polyester-polyurethane polymer binder.
    [0011]
    11. Method according to claim 9, characterized in that the nanoparticles are dispersed with one or more dispersants.
    [0012]
    12. Use of a clear coating composition as defined in any one of claims 1 to 8, characterized in that it is for coating substrates.
    [0013]
    13. Coated substrate, characterized in that it is coated with a clear coating composition as defined in any one of claims 1 to 8 in which the substrate is selected from porous and non-porous substrates, including papers, non-woven materials, textiles , leather, wood, concrete, masonry, metals, house wrap and other building materials, fiberglass, polymeric articles, personal protective equipment, rugs, textiles used in clothing, upholstery, tents, awnings, air bags, fabrics , yarns and blends, whether woven, non-woven, or knitted, and naturally occurring, synthetic or regenerated.
    [0014]
    14. Coated substrate according to claim 13, characterized in that the coated substrate includes papers and non-wovens, fibrous materials, films, sheets, composites, printing inks, pastes, flake and other adhesives and personal hair care products including hygiene products for skin care, hair care, nail care, livestock and food applications.
    [0015]
    A coated substrate according to claims 13 or 14, characterized in that the coating composition is applied to the substrate in an amount so as to form a layer having a thickness of between 100 and 400 nm.
    [0016]
    16. Method of forming a coated substrate coated with a coating composition, characterized in that a clear coating composition as defined in any one of claims 1 to 8 is applied to the substrate.
    [0017]
    17. Method according to claim 16, characterized in that the coating composition is applied to the substrate by coating, impregnation or otherwise treatment.
    [0018]
    18. Method according to claim 16, characterized in that the clear coating composition is applied to the substrate in an amount so as to form a layer with a thickness between 100 and 400 nm.
    [0019]
    19. Method according to claim 16 or 17, characterized in that the coated substrate is further dried and optionally cured.
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    CA2825581C|2018-09-25|
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    BR112013021170A2|2018-04-03|
    HUE031180T2|2017-06-28|
    AU2012219504B2|2015-11-26|
    UY33917A|2012-09-28|
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    法律状态:
    2018-04-17| B06F| Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]|
    2020-02-27| B06U| Preliminary requirement: requests with searches performed by other patent offices: procedure suspended [chapter 6.21 patent gazette]|
    2020-09-08| B06A| Notification to applicant to reply to the report for non-patentability or inadequacy of the application [chapter 6.1 patent gazette]|
    2021-04-06| B09A| Decision: intention to grant [chapter 9.1 patent gazette]|
    2021-05-11| B09X| Decision of grant: republication|
    2021-05-25| B16A| Patent or certificate of addition of invention granted|Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 23/02/2012, OBSERVADAS AS CONDICOES LEGAIS. |
    优先权:
    申请号 | 申请日 | 专利标题
    US201161446006P| true| 2011-02-23|2011-02-23|
    US61/446006|2011-02-23|
    US61/446,006|2011-02-23|
    PCT/EP2012/053089|WO2012113876A1|2011-02-23|2012-02-23|Coating composition comprising submicron calcium carbonate-comprising particles, process to prepare same and use of submicron calcium carbonate-comprising particles in coating compositions|BR122015001925-7A| BR122015001925B1|2011-02-23|2012-02-23|COATING COMPOSITION, METHOD OF FORMATION OF A COATING COMPOSITION, USE OF A COATING COMPOSITION, COATED SUBSTRATE, AND, METHOD OF FORMATION OF A COATED SUBSTRATE|
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