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    • 专利摘要:
    The present invention relates to a colored luminescent composite pigment comprising, in combination, at least one luminescent pigment having a mean particle size of between 50 and 2000 μm, and at least one dye. The present invention also relates to compositions and materials comprising this pigment, its method of preparation and its use for coloring materials, especially hydraulic binder composition.
    公开号:FR3041651A1
    申请号:FR1559270
    申请日:2015-09-30
    公开日:2017-03-31
    发明作者:Jean-Jacques Hivert
    申请人:Chryso SAS；
    IPC主号:
    专利说明:

    Colored luminescent pigment, process for its preparation and uses thereof
    The present invention relates to colored luminescent pigments, processes for their preparation, compositions comprising them, coatings comprising them, and their uses, in particular in hydraulic binder compositions. The introduction of luminescent pigments in materials, in order to provide visibility in low light or zero brightness (night, shadow, darkness, interior unlit due to an electrical failure ...), is sought. The goal is to provide good visibility over a long period, typically over several hours. This is particularly of interest for signaling type applications, for example vertical or horizontal; extra lighting, improvement of the aesthetics of a material, for example graphic visualization, decoration ...
    However, it may be desired to choose the color of the material when the material is in the light and when the material is in a low light or zero brightness location, typically for illuminations less than 100 Ix or even 10 Ix or even less than 1 Ix. For example, it may be desired to have a different color when the material is in the light and when the material is in a low light or zero brightness location. It is therefore necessary to provide a pigment or a pigment composition combining at least one luminescent pigment and at least one so-called conventional dye.
    Many technologies have been developed in this direction.
    It is in particular known from JP201240596 the application of at least two successive coatings on the material. A first layer, in contact with the material, comprising a luminescent pigment and a second layer, deposited on top of the first layer, comprising a conventional dye. However, this technology requires the application of different coatings, time consuming and economically unprofitable. In addition, there may be adhesion problems of different coatings.
    An alternative technology proposes to introduce, in the same essentially transparent matrix, in particular plastic matrix, glass ..., the luminescent pigment and the dye. This technology is described in particular in US20050096420. However, the luminescent pigment and the dye being dispersed independently, the effect of the dye is not very effective which imposes a high dosage.
    In an attempt to overcome this problem, it has been proposed to associate more intimately the luminescent pigment and the dye. In particular, US2005 / 0035331 describes the combination of a luminescent pigment with a highly reflective material such as titanium dioxide. However, the effect that was sought was to enhance the luminescence and not to combine the luminescence with a color in the light. The association between a phosphorescent pigment A and a dye B is also described in WO2009053391, the size of the pigments A being between 0.5 and 25 μm and the size of the dyes B being less than 0.2 μm. However, the remanence time obtained is only a few seconds and this technology requires a high content of dye B affecting the efficiency of the system because this dye B will absorb the light used to charge the phosphorescent pigment A and also that emitted by pigment A in the dark.
    The present invention aims in particular the treatment of composition based on hydraulic binder and in particular concretes. This particular application can bring additional stress due to the alkaline pH of the hydraulic binder compositions. The introduction of luminescent pigments into concretes is already described, in particular in FR2168685, FR2990204 and WO2010134805. However, these documents do not describe the possibility of introducing a particular dye to choose and control the color of concrete in light and low light or zero brightness.
    There is therefore an interest in providing a colored luminescent pigment, which can be used in particular in the mass of the material, which makes it possible to control a coloration of the material with light and that obtained by luminescence in low light or in the absence of luminosity, without significantly disrupt the efficiency of the luminescent effect of the luminescent pigment alone.
    An object of the present invention is to provide a colored luminescent pigment, especially usable in the mass of the material, which allows the control of a coloration of the material in the light and by luminescence in low light or in the absence of brightness.
    Another object of the present invention is to provide a process for the preparation of such a pigment.
    It is another object of the present invention to provide compositions comprising the colored luminescent pigment.
    Still another object of the present invention is to provide a material, for example a paint, a hydraulic binder composition, comprising the colored luminescent pigment or the composition comprising the colored luminescent pigment. Other objectives will appear on reading the description of the invention which follows.
    In order to meet the disadvantages of the prior art mentioned above, the present invention provides a colored luminescent composite pigment comprising at least one luminescent pigment and at least one dye, the composite pigment having an average particle size of between about 50 and about 2000 pm.
    The composite pigment of the present invention may also be defined as a colored luminescent composite pigment comprising, in combination, at least one luminescent pigment and at least one dye, and having an average particle size of from about 50 to about 2000 μm.
    Preferably, the colored luminescent composite pigment according to the present invention (or colored luminescent pigment or composite pigment or luminescent composite pigment) has an average particle size of from about 60 to about 2000 μm, preferably from about 60 to about 500 μm, for example between about 75 and about 200 microns.
    In the context of the present invention, the term "luminescent pigment" is understood to mean any compound capable of absorbing photons emitted by natural or artificial light and render a light emission in the case of reduced brightness or in the absence of luminosity. . Luminescence includes phosphorescence and fluorescence. Preferably, in the context of the present invention, the luminescent pigment is a photoluminescent pigment.
    The luminescent pigment will be chosen according to the color, in reduced brightness or in the absence of brightness, which is desired.
    Preferably, the luminescent pigment will be selected to have a remanence of several hours after exposure to natural or artificial light.
    In general, the luminescent pigment may be organic or inorganic, the mineral pigments being preferred because of their greater durability, especially in the open air.
    The luminescent organic pigments are chosen in particular from naphthalimides, coumarins, xanthenes, thioxanthenes, naphtholactams, azlactones, methines, oxazines and thiazines, or their mixture.
    The inorganic luminescent pigments are chosen in particular from: sulphides, such as, for example, CaS: Bi, CaSrS: Bi, ZnS: Cu, ZnS: Pb2 +, ZnS: Mn2 +, ZnCdS: Cu, AB2S4 (where A = alkaline earth metal B = aluminum), ZnS, ZnS: Ag, ZnS: Cu: Cl, ZnS: Cu: Al, (Ce3 (SiS4) 2X (where X = Cl, Br, I), La3-xCex (SiS4) 21 (where 0sx <1), SrS: Cr, SrS doped with rare earths where Mn, CdS: Mn, Y2O2S: (Er, Yb); fluorides, for example, AF3 (where A = La3 +, Ce3 +, Y3 +) and AF2 (Al3 +, Mg2 +, Ca2 +, Pb2 +) and containing at least one luminescent ion selected from the group consisting of trivalent metal ions (Cr3 +, Fe3 +, etc.) or rare earths (Y3 +, Pr3 +, Nd3 +, Sm3 +, Eu3 +, Tb3 + , Dy3 +, Ho3 +, Er3 +, Tm3 +, Yb3 +), LnF3, ALnF4, ALn2F8, ALn3F10 (where Ln = rare earth or yttrium, a monovalent alkaline ion, and containing at least one luminescent ion selected from the group consisting of trivalent metal ions ( Cr3 +, Fe3 +, etc.) or rare earths (Y3 +, Pr3 +, Nd3 +, Sm3 +, Eu3 +, Tb3 +, Dy3 +, Ho3 +, Er3 +, Tm3 +, Yb3 +), EF3 (E = G a3 +, ln3 +, Bi3 + and containing at least one luminescent ion selected from the group consisting of trivalent metal ions (Cr3 +, Fe3 +, etc.) or rare earths (Y3 +, Pr3 +, Nd3 *, Sm3 +, Eu3 +, Tb3 +, Dy3 +, Ho3 + , Er3 +, Tm3 +, Yb3 +), Sn-xEu ^ SiFe1-MD (where 0 <x ^ 0.5), M1-xEUx2 * SiF6 (where 0 <x ^ 0.2 and M is selected in particular from calcium and barium), K2YF5 (doped with Gd3 +, Tb3 +, Eu3 + or Pr3 +), LiYF4 (doped with Gd3 +, Tb3 +, Eu3 + where Pr3 +), NaLnF4 (where Ln = lanthanide or Y), NaYF4: Pr3 +, Na (Y, Yb ) F4: Pr3 +, Na3AIF6 containing at least one luminescent ion selected from the group consisting of trivalent ions (Cr3 +, Fe3 +, etc.) or rare earths (Y3 +, Pr3 +, Nd3 +, Sm3 +, Eu3 +, Tb3 +, Dy3 +, Ho3 +, Er3 + , Tm3 +, Yb3 +), BaLiF3: Eu3 +, BaY2F8: Eu3 +, BaSiF6: Eu3 +, [alpha] -NaYF4: Pr3 + or LiGdF4: Eu3 +; luminescent oxides, for example MAI204 (where M = one or more metals chosen from calcium, strontium and barium, the oxide may be doped with europium as a luminescence activator and may optionally contain other activators, for example lanthanum, cerium, praseodymium, neodymium, samarium, gadolinium, dysprosium, holmium, erbium, thulium, ytterbium, lutetium or tin and bismuth as co-activators in SrAI204 (Eu2 +, Dy3 +), (M'xM''y) AI204 (where x + y = 1 and M 'and M "are different and selected from calcium, strontium and barium, the oxide being doped with europium as an activator and possibly containing other activators such as lanthanum, cerium, praseodymium, neodymium, samarium, gadolinium, dysprosium, holmium, erbium, thulium, ytterbium, lutetium or tin and bismuth as coactivators, Μ1. ΑΙ204-χ (ού M is at least one metal selected from calcium, strontium and barium or in which M comprises magnesium and at least one metal selected from calcium, strontium and barium, where x is non-zero and preferably between -0.3 and 0.6, the oxide may be doped with europium as an activator and may optionally contain other activators, such as, for example, lanthanum, cerium, praseodymium, neodymium, samarium, gadolinium, dysprosium, holmium, erbium, thulium, ytterbium, lutetium or tin and bismuth as coactivators, LnB03 where Ln = at least one rare earth, M4AI14025 where M = one or more metals selected from calcium, strontium and barium, the oxide may be doped with europium as an activator and may optionally contain other activators such as lanthanum, cerium, praseodymium, neodymium, samarium, gadolinium, dysprosium, holmi um, erbium, thulium, ytterbium, lutetium, or tin and bismuth as coactivators), M ^ l)! - xEu (ll) xM (III) pEu (III) qTb (III) wherein M (II) is at least one bivalent metal selected from barium, strontium, lead and calcium, M (III) is selected from lanthanum, gadolinium, yttrium, cerium, lutetium and bismuth, 0 ^ 0.2, p, q and r are harmless, strictly between -1 and 1 such that p + q + r = 1, υν xTbxMgB5Oio where Ln = rare earth or yttrium and 0 <x <1, ## EQU1 ## where M = Bai-bSrb, 0ib1, 0, 0 <a <0.2 and X = Cli-cBrc where 0 <c1, La1.xSmxOBr (where 0 <x < 0.1), ZnO: Zn, ZnO: Ga203: Bi, CaTiO3: Pr3 +, La2Ti05: Pr3 +, La2Ti207: Pr3 +, (La, Pr) 2Ti207, (La, Yb, Pr) 2Ti207, YB03: (Eu3 +, Tb3 +, Gd3 +), Y3B06: Eu3 +, LnB03 (doped with Eu3 +, Tb3 +, Pr3 + or Tm3 +, doped or co-doped with Ce3 + or Gd3 + and Eu3 +, Tb3 +, Pr3 +, Tm3 + or Pr3 +), Ln3B06 (doped with Eu3 +, Tb3 +, Pr3 + or Tm3 *, doped or co-doped with Ce3 + or Gd3 + and Eu3 +, Tb3 +, Pr3 +, Tm3 + or Pr3 +), Ln (B02) 3 (doped with Eu3 +, Tb3 +, Pr3 + or Tm3 +, doped or co-doped with Ce3 + or Gd3 + and Eu3 +, Tb3 +, Pr3 +, Tm3 + or Pr3 +), Si02 (doped with rare earths), SiO2: (Sm3 +, Al3 +), Al (2_x_y) (Y , Where M = Cr 2 O 3, V 2 O 5, NiO, WO 3, CuO, FeO, Fe 2 O 3 and Ln = Er, La, Yb, Sm, Gd and mixtures thereof and 0.48 <x <1.51 and 0.007 <y <0.2), Al203 (doped with rare earths), - phosphate glasses (doped with rare earths), LiNbO3 (doped with rare earths), TiO 2 (doped with rare earths), LaPO4 : Ce and / or Tb, LaPO4: Eu,
    CePO4: Tb, MAI2B207: Eu2 + (where M = Sr, Ca), M2B509X: Eu (where M = Ca, Sr, Ba and X = Cl, Br), CaSO4: Eu, CaSO4: Eu, LaMgB5OiO: Ce where Mn, Y203: Eu, Gd2O3: Eu, (Yo.7Gdo3) 203: Eu, CoAl2O4, Mg4Ge05.5F: Mn, (Sr, Mg) 3 (PO4) 2: Sn, Y3Al5O12: Ce, BaMgAl10O17: Eu, BaMg2Al16027: Eu (Ce, Tb) MgAlnOi9, (Ce, Gd, Tb) MgB5O1, (Ce, Gd, Tb) MgB5O1: Mn, LaPO4: (Ce, Tb), Sr2Al14025: Eu,
    Ca5 (PO4) 3 (F, Cl) :( Sb, Mn), (La, Ce, Tb) (PO4) 3: (Ce, Tb), CeO0.65TbO0.35MgAl11O191 barium-titanium phosphates, (Ba, Sr, Ca, 2SiO 4: Eu, SrAl 2 O 19 19: Ce, BaSi 2 O 5: Pb, (Sr, Zn) MgSi 2 O 7: Pb, SrB 4 O 7: Eu, (Gd, La) B 3 O 6: Bi, Sr 2 P 2 O 7: Eu, BaMgAl 2 O 17: Eu, Mn, Zn 2 SiO 4: Mn, YV04: (Eu, Sm, Dy), AWO4 (where A = Ca, Ba, Pb, Cd, Zn, Mg), In203: (Er, Tb), GdAI (B03) 4: Nd, ZrO2: Eu3 +, GdVO4: (Bi, Eu); - red phosphorus; and the nitrites of alkali or alkaline earth metals.
    Preferably, the luminescent pigment is chosen from zinc sulphide and strontium aluminates doped with rare earths.
    Preferably, the luminescent pigments according to the present invention are not covered with a protective layer, that is to say they have not been covered with a polymeric matrix (for example polyethylene), an wax ... to protect them from external aggressions, especially to protect them from reactions to water. Indeed, as has been shown by the inventors, if pretreated luminescent pigments coated with a protective layer are used in the invention, when the composite pigment obtained is washed with water, the water is found colored dye color, thus highlighting leaching of the dye. This also shows that there is indeed an intimate association in the composite pigment of the invention between the luminescent pigment and the dye. Preferably, the luminescent pigment has an average particle size of from about 60 to about 2000 μm, preferably from about 60 to about 500 μm, for example from about 75 to about 200 μm.
    Preferably, the luminescent pigment particles are porous and have a percentage of pores by volume, in particular measured by mercury porosity according to the IS015901-1: 2005 standard, of between 1 and 90%, preferably between about 2 and about 50%. .
    In the context of the present invention, the term "dye" is understood to mean a substance, or a mixture of substances, which makes it possible, when it is used in a material, to give a color to this material. absorbing or reflecting specific wavelength radiation. This substance or mixture may be soluble or insoluble in the material in question.
    In the context of the present invention, the dye will make it possible to fix the color of the material in the light, in particular in the light of the day. The dye will be chosen according to the desired color, it is also possible to use dye mixtures. The dye may be organic or inorganic in nature. The dye may especially be in the form of a powder, a powder in suspension.
    The organic dyes may especially be chosen from compounds nitroso (compound comprising a group NO), nitro (compound comprising a group NO2), azo (compound comprising a group HN = NH), xanthene, quinoline, anthraquinone, phthalocyanine, complex type metal, isoindolinone, isoindoline, quinacridone, perinone, perylene, diketopyrrolopyrrole, thioindigo, dioxazine, triphenylmethane, quinophthalone. These dyes are known to those skilled in the art. These dyes may also be in the form of composite dyes as described for example in patent EP 1 184 426. This composite dye may be composed in particular of particles comprising an inorganic core, at least one binder ensuring the fixation of organic dyes. on the core, and at least one organic dye at least partially covering the core. The dye may also be a special effects dye. Special effects dyes are dyes which generally create a colored appearance (characterized by a certain shade, a certain liveliness and a certain clarity) which is non-uniform and changeable according to the conditions of observation (light, temperature , observation angles ...). They are therefore opposed to white or colored dyes that provide a uniform opaque, semi-transparent or conventional transparent tint. As special effect pigments, mention may be made of pearlescent pigments such as white pearlescent pigments such as titanium mica, or mica-bismuth oxychloride, colored pearlescent pigments such as titanium mica with iron oxides, mica titanium with in particular ferric blue or chromium oxide, titanium mica with an organic pigment of the aforementioned type as well as pearlescent pigments based on bismuth oxychloride.
    As inorganic dyes, mention may be made of titanium oxides such as anatase and rutile, the various iron oxides (yellow, red, brown, etc.), chromium oxides, barium oxides, oxides of cadmium, nickel oxides, copper oxides, cobalt oxides, zinc oxides, cobalt stannate, cobalt aluminates, quartz powder, talc, carbon black, calcium carbonate and barite.
    The dye may also be a fluorescent dye (or brightener). Such fluorescent dyes may be of interest, especially for safety displays. The effect of the dye can be enhanced by combination with an optical brightener for example. This brightener (or combination of brighteners) may for example be chosen from stilbene derivatives.
    Preferably, the dye is chosen from oxides of iron, barium, chromium, cadmium, zinc, cobalt, nickel and titanium and carbon black.
    Preferably, in the context of the present invention, for insoluble dyes, the size of the dye particles is smaller than the size of the luminescent pigment particles. Preferably, the average size of the dye particles is at least 10 times smaller than that of the luminescent pigment. Preferably, the dye has an average particle size of from about 0.1 to about 10 microns.
    In the context of the present invention, the mean size of the particles or aggregates, the mean diameter of the particles. This size can be measured in terms of volume by laser particle size for particles having a size of less than or equal to 500 μm (ISO 13320: 2009 standard) or by weight by sieving for particles having a size greater than 500 μm (measured according to the NF standard). EN 933-1 of May 2012).
    The expression "control of the coloring with the light and control of the luminescence in low light or in the absence of brightness", the fact to have a homogeneous color with the light and to have a homogeneous color by luminescence under low illumination (or low light) or in the absence of illumination (or in the absence of brightness), these colors being identical or different and being chosen independently of one another.
    In the context of the present invention, low luminosity (or low illumination) and absence of luminosity (or absence of illumination) are understood to mean illuminances less than 100 Ix, even 10 Ix or even less than 1 Ix.
    By "association" is meant an interaction, particularly intimate, between the luminescent pigment and the dye which allows, when the colored luminescent pigment is rinsed with water not to remove the dye as has been shown by the inventors.
    Preferably, the composite pigment according to the invention comprises from 0.00001 to 99.99999% by weight of luminescent pigment and from 99.99999 to 0.00001% by weight of dye, preferably from 50 to 99.99% by weight of luminescent pigment and from 50 to 0.01% by weight. by weight of dye.
    The present invention also provides a method for preparing a colored luminescent composite pigment comprising the steps of: a) providing a composition comprising one or more dyes in a fluid; b) mixing with the composition of step a) at least one luminescent pigment; and c) drying the mixture obtained in step b).
    Preferably, the composition of step a), when the dye is non-soluble in the fluid, is a dye suspension (s) in the fluid.
    Preferably, the fluid is selected from water, alcohols (preferably ethanol) and acetone, or mixtures thereof. Preferably the fluid is water and in particular purified water (by distillation or passage over an ion exchange resin) in order to avoid the appearance of whitish deposit on the colored luminescent pigment and to limit the phenomena of agglomeration detrimental.
    The dye may be suspended or solubilized in the fluid by any means known to those skilled in the art, in particular by mechanical means. Suspending can also be carried out in the presence of a surfactant-type dispersant or other polymers, for example acrylic polyacid, comb polymer, in particular of the PCP type, structured polymer such as those described in the patent application EP0877765.
    The composition of step a) may optionally contain a wetting agent. Such wetting agents are described in particular in the reference: The formulation of paints, J.C.Laout, Ed. Engineering Techniques, page J 2 270-16 of September 10, 2005.
    Preferably, in the context of the present invention, the composition of step a) comprises from 0.0001 to 50%, preferably from 0.05 to 1%, preferably from 0.1 to 0.5%, by weight of dye (s) relative to the total weight of the composition. This advantageously makes it possible to control the viscosity of the composition of step a).
    Preferably, the Brookfield dynamic viscosity of the composition of step a), measured at 20 ° C., is less than 1000 mPa.s, preferably less than 100 mPa.s, in particular between about 1 mPa.s and 1000 mPa. .s, preferably between about 1 mPa.s and about 100 mPa.s. The inventors have pointed out that the more the composition of step a) was viscous, the more the composite pigment was leachable with loss of the dye, revealing a less good association, or even a gap between the luminescent pigment and the dye at viscosities. greater than 1000 mPa.s.
    Preferably, the composition of step a) is an aqueous dye composition.
    Preferably, in step b), the luminescent pigment is as defined above.
    Preferably, the amount of dye is chosen so that the loss of luminescence of the final colored luminescent pigment with respect to the luminescent pigment alone is not greater than 10% (loss measured according to NF X 08-050-1 and DIN 6751 ΟΙ). Preferably, in step b), the mixture obtained comprises 1 to 90%, preferably 15 to 60%, preferably 25 to 35%, by weight of luminescent pigment relative to the total weight of the mixture.
    Additional additives, for example color enhancers or antioxidants, may be added during step b), especially in contents of 0.1% to 5% by weight relative to the weight of the mixture obtained in step b). Color enhancers may be chosen in particular from fatty acids. The antioxidants may in particular be chosen from phenol derivatives, aromatic secondary amines, quinones, amines of HALS (Hindered Amine Light Stabilizers) type.
    Advantageously, the mixture of step b) is carried out for 30 seconds to 1 hour, preferably for 1 to 10 minutes. The agitation, during step b), should preferably not be shearing so as not to change the size of the luminescent pigments and dyes. Stirring greater than 10 minutes may cause a risk of luminescent pigment breaking and risk of agglomeration. Stirring less than 1 minute can cause a less good association between the luminescent pigment and the dye and thus a possible leaching of the composite pigment obtained.
    Without wishing to be bound by any theory, during this step b) the dye is associated with the luminescent pigment to form the colored luminescent pigment. In order to improve the association between the dye and the luminescent pigment, step b) can be carried out in the presence of a binder. Among the binders that may be mentioned include latexes, epoxy resins, polyurethane resins. The drying step c) can be carried out at room temperature (about 20 to 25 ° C), however the temperature must be controlled in order not to degrade luminescent pigments and dyes. Those skilled in the art, in view of the luminescent pigments and dyes used, are able to determine the drying limit temperature.
    Preferably, the drying temperature is below 400 ° C.
    The drying can be carried out by any method known to those skilled in the art and in particular by static drying (for example drying in a fixed thin layer), atomizer, fluidized bed, etc.
    Preferably, the drying step can be carried out under a gaseous flow, for example air flow, nitrogen. The drying step c) can also be carried out under vacuum. Advantageously, this reduces the drying time.
    The method according to the present invention may comprise, before step c), a step b ') of decanting the mixture obtained in step b) and of separating: a solid phase comprising the composite pigment according to the invention which is then dried in step c) and; a liquid phase comprising the dye which has not been associated with the luminescent pigment and which can be reused in the process of the invention as a composition of stage a).
    The process for preparing the colored luminescent pigment according to the present invention may also comprise a step b "), before or after step c), and if appropriate before or after step b '), of depositing a coating on the surface of the colored luminescent pigment. This step, which advantageously makes it possible to protect the colored luminescent pigment, in particular with respect to water, can be carried out hot or cold, in particular up to a temperature of 400 ° C., per known method. those skilled in the art such as spraying or quenching in a bath. The coating may be chosen by those skilled in the art depending on the application and the final material referred to. The coating may especially be a polymeric coating (chosen in particular from polyurethanes, epoxy resins, acrylic polymers, polyamides, polyesters, silicone resins, polyalkylenes or fluorinated polymers) or a wax (chosen especially from natural origin such as carnauba wax or synthetic waxes such as paraffins). In this case, it is possible to coat the colored composite phosphor pigment of the invention by mixing this pigment in a composition comprising the polymer or resin or a monomer capable of polymerizing to form the desired polymer. Thus, if the polymer, monomer or resin composition is a composition of the same type as the composition of step a) then step b ") can be carried out before step b ') and before step vs). The invention also relates to the colored luminescent pigment obtainable by the method of the invention.
    The colored luminescent pigment of the present invention may be introduced into a matrix, preferably transparent.
    The present invention therefore relates to a luminescent composition (C) comprising a transparent matrix and a luminescent composite pigment according to the invention.
    Preferably, the transparent matrix is in particular compatible with the alkaline pH of the hydraulic binder compositions, and is preferably chosen from polymethyl methacrylate (PMMA), polycarbonate (PC), polyvinyl chloride (PVC), polyurethane ( PU), styrene acrylonitrile (SAN) copolymers and their derivatives such as ABS (acrylonitrile / butadiene / styrene) or glass.
    The luminescent composition (C) may be a liquid composition or a solid composition at room temperature (approximately 20 to 25 ° C.), that is to say that the transparent matrix that it contains is either a transparent liquid matrix at ambient temperature is a transparent matrix solid at room temperature.
    Advantageously, the luminescent composition (C) is a solid composition, the solid transparent matrix notably making it possible to ensure durability and to avoid degradation, in particular by contact with water, of the colored luminescent composite pigment.
    The luminescent composition (C) may be obtained by dispersing the colored luminescent pigment obtained in step c) in a liquid transparent matrix solution or in a transparent liquid matrix capable of generating the solid transparent matrix, in particular by solidification, crosslinking or polymerization. .
    When the luminescent composition (C) is solid, it can be molded, for example the mold can be filled by an injection press, or shaped by extrusion.
    By solution capable of generating the transparent matrix is meant the transparent matrix in the molten state (which can therefore generate the transparent matrix by solidification), or a solution comprising monomers capable of generating the transparent matrix by polymerization, or a solution comprising a prepolymer capable of generating the transparent matrix by crosslinking.
    Preferably, the solution capable of forming the transparent matrix is a solution of molten polymer or molten glass, preferably molten polymer. Advantageously, this makes it possible, because of the high viscosity of the molten polymer, to avoid settling of the composite pigment according to the invention and thus to obtain homogeneous compositions.
    The luminescent composition according to the invention comprises from 0.001% to 99.999% by weight of luminescent composite pigment and 99.999% to 0.001% by weight of transparent matrix. Preferably, the luminescent composition comprises between 0.5% and 60% by weight of luminescent composite pigment and 99.5% and 40% of transparent matrix, and preferably between 5% and 50% of luminescent composite pigment and 95% and 50% by weight of transparent matrix.
    The solid luminescent composition (C) obtained can be milled to form aggregates. The grinding can be carried out by any method known to those skilled in the art depending on the size of the desired aggregates. The invention therefore also relates to a granulate comprising a transparent matrix and a composite pigment according to the invention. Preferably, the aggregates have an average particle size of between about 0.1 and 125 mm (size measured according to the standards ISO 13320: 2009 or NF EN 933-1 of May 2012).
    In a particularly preferred manner, the transparent matrix is PMMA and the solution capable of forming the transparent matrix is a molten PMMA solution. In a preferred embodiment, the mixture of molten PMMA and composite pigment according to the invention is poured into a mold, in particular using an injection molding machine. Preferably, after demolding, the composition (C) obtained is milled to obtain aggregates of desired size.
    In a particular embodiment, the process for preparing the composition (C) of the invention or a granulate of the invention comprises the steps of: 1) providing a colored luminescent composite pigment according to the invention; 2) dispersing the colored luminescent composite pigment in a solution capable of forming the transparent matrix; 3) optionally formatting the dispersion obtained in step 2), in particular in a mold; 4) optionally solidifying the mixture obtained in step 2) or 3); 5) optionally grinding the composition obtained in step 4) to obtain aggregates.
    The method may comprise a step of preparing the colored luminescent composite pigment according to the invention before step 1), in particular the preparation method described above.
    In a particularly preferred embodiment, the invention relates to a process for preparing a granulate according to the invention wherein the transparent matrix is PMMA, comprising the steps of: 1) providing a colored luminescent composite pigment according to the invention ; 2) dispersing the composite pigment in a solution of melted PMMA; 3) shaping the dispersion obtained in step 2) in a mold, in particular using an injection molding machine; 4) solidification of the mixture obtained in step 3); 5) grinding of the composition obtained in step 4).
    The method may comprise a step of preparing the colored luminescent composite pigment according to the invention before step 1), in particular the preparation method described above.
    Advantageously, the composition (C) according to the invention, or the granulate according to the invention, can also comprise additives, in particular additives of flame retardant type; additives which improve the hardness, for example quartz.
    These additives are preferably added during the preparation of the luminescent composition (C) or the granulate, especially in the dispersion comprising the composite pigment of the invention and the solution capable of forming the transparent matrix.
    The colored luminescent composite pigment and the luminescent composition (C) according to the present invention, optionally in the form of granules, can be used for coloring materials such as hydraulic binder compositions (plaster, concrete, mortar, screed), plastics, plaster, coatings, varnishes and paints, inks, paper and cardboard, cosmetic compositions, textiles, glasses, enamels, ceramics, tile adhesives, tile joints ...
    The coloration with the colored luminescent pigment of the invention, the composition (C) of the invention or the granulate of the invention can be made both in the mass and on the surface of the material to be colored. In the case of a surface application, the composite pigment according to the invention can be used: in a two-component mixture comprising, on the one hand, the composite pigment, the composition (C) or the granulate, and on the other hand a binder, the mixture of the two components being made just before the application - in a one-component mixture comprising the composite pigment, the composition (C) or the granulate dispersed in a binder, in particular of the acrylic, epoxy, styrene- acrylic, silicate, polyurethane, ... The surface application can be done by spraying, by deposition for example by roller or with a brush, by pouring, by dusting (in particular dusting of the composite pigment on the surface of the material). When the composition (C) is liquid, it can be applied by spraying, by deposition for example by roll or deposition on the surface of the material and crosslinking or polymerization to form a solid coating. Advantageously, for a surface application, the composite pigment can be dispersed in a solution of a monomer capable of polymerizing after deposition on the surface of the material.
    With regard to the composition (C) or the granulate, the surface application can be done for example by nailing (insertion of a composition (C) or granulate on the surface of the material before setting). The invention also relates to a material comprising the colored luminescent composite pigment or the luminescent composition (C) or the granulate according to the invention.
    Preferably, the material is chosen from hydraulic binder compositions (plaster, concrete, mortar, screed), plastics, varnishes and paints, coatings, coatings, inks, paper and paperboard, cosmetic compositions, textiles, glass, tile adhesives, tile joints ...
    Preferably, the use of the composite pigment according to the invention, of the composition (C) according to the invention or of the aggregates according to the invention makes it possible to obtain materials of homogeneous color with good control of the color at the light and in reduced brightness or in the absence of brightness while reducing the necessary amount of dye compared to the usual techniques.
    The present invention also relates to a coating comprising the colored luminescent composite pigment or the composition (C) or the granulate according to the present invention. The coatings may for example be organic coatings, for example acrylic coatings, or inorganic coatings, for example silicate paint. The coatings can also be obtained by a sol / gel process.
    In a particularly preferred manner, the present invention relates to the use of composite pigments according to the invention and / or aggregates according to the invention for the coloration of hydraulic binder compositions, especially for the coloring of concrete.
    The term "hydraulic binder" is understood to mean any compound having the property of hydrating in the presence of water and whose hydration makes it possible to obtain a solid having mechanical characteristics. The hydraulic binder can comprise or consist of a cement according to the EN 197-1 standard and in particular a CEM I, CEM II, CEM III, CEM IV or CEM V type cement according to the NF EN 197-1 (2012) cement standard. The cement can therefore in particular comprise mineral additions.
    The term "composition based on hydraulic binder" means a composition comprising a hydraulic binder. It may be a composition based on fresh hydraulic binder, which then corresponds to a "hydraulic binder composition", or a composition based on hardened hydraulic binder, such as concrete.
    The hydraulic binder can also be a hydraulic binder based on calcium sulphate. By the term "calcium sulfate hydraulic binders" is meant according to the invention the hydraulic binders based on partially anhydrous or totally anhydrous calcium sulfate. This includes: - Gypsum or calcium sulfate hydrate: CaSO4.2 (H20); - Calcium sulphate hemihydrate or calcium sulphate hemihydrate or partially anhydrous calcium sulphate: CaSO4.0.5H2O; - anhydrous calcium sulphate or anhydrite or totally anhydrous calcium sulphate: CaSO4.
    The term "fresh" refers to such hydraulic binder-based compositions when they have been tempered with water, but have not yet hardened. They are then malleable enough to fill the mold or formwork.
    The term "hardened" is understood to mean such hydraulic binder-based compositions when cured.
    By the term "setting" is meant the passage to the solid state by hydration reaction of the binder.
    By the term "concrete" is meant a mixture of hydraulic binders, aggregates, sands, water, optionally additives, and possibly mineral additions. The term "concrete" also includes mortars and screeds. The term "mineral additions" refers to slags (as defined in NF Cement Standard EN 197-1 (2012) section 5.2.2), steelmaking slags, pozzolanic materials (as defined in NF Cement Standard). EN 197-1 paragraph 5.2.3), fly ash (as defined in standard Cement NF EN 197-1 paragraph 5.2.4), calcined schists (as defined in standard Cement NF EN 197-1 paragraph 5.2 .5), limestones (as defined in standard Cement NF EN 197-1 paragraph 5.2.6) or even fumes of silicas (as defined in standard Cement NF EN 197-1 paragraph 5.2.7) or their mixtures. Other additions, not currently recognized by the standard Cement NF EN 197-1 (2012), can also be used. These include metakaolins, such as type A metakaolins conforming to standard NF P 18-513, and siliceous additions, such as the siliceous additions of mineralogy Qz conforming to standard NF P 18-509 (2012). .
    By the term "aggregates" is meant a set of mineral grains with a mean diameter of between 0 and 125 mm. Depending on their diameter, aggregates are classified into one of six families: fillers, sand, sands, gravels, chippings and ballast (standard XP P 18-545 of September 2011). The most widely used aggregates are: fillers, which have a diameter of less than 2 mm and for which at least 85% of the aggregates have a diameter of less than 1.25 mm and at least 70% of the aggregates have a diameter less than 0.063 mm, sands with a diameter between 0 and 4 mm (in standard 13-242, diameter up to 6 mm), lobes with a diameter greater than 6.3 mm, gravel diameters between 2 and mm and 63 mm. Sand is therefore included in the definition of granulate according to the invention. The fillers may in particular be of calcareous, siliceous or dolomitic origin.
    The present invention also relates to hydraulic binder compositions, preferably concrete, comprising the colored luminescent composite pigment of the invention and / or the aggregates of the invention.
    When the colored luminescent composite pigment is used, it can be introduced into the mass of the hydraulic composition, especially concrete, or at the surface of the hydraulic composition. For introduction into the mass, the composite pigment according to the invention can be added in premix with the standard aggregates and introduced to the mix or directly introduced, individually at the time of mixing. The quantities of composite pigment used depend on the color and in particular on the intensity that is desired. In general, they correspond to the amounts generally used for conventional dyes, that is to say between 1 and 10% by weight of the hydraulic binder. For a surface application, the composite pigment of the invention can be sprinkled on the surface of the hydraulic binder composition before setting or applied, before or after setting dispersed in a composition of paint type, varnish.
    When the aggregates according to the invention are used, they can be used as a replacement for all or part of the aggregates typically used in hydraulic compositions, particularly of the concrete type or in addition to the aggregates typically used. Aggregates can also be inserted into the concrete surface before setting.
    The present invention will now be described with the aid of figures and non-limiting examples.
    Figure 1 shows the particle volume in% versus particle size in μm and provides the particle size distribution measured by laser particle size (Mastersizer 2000) (Example 7).
    FIG. 2 represents the granulometric curve of the aggregates according to the standards NF EN 933-1 and NF EN 933-2 (example 8).
    Example 1 3 g of yellow ocher dye (from the brand Universal Dye) are dispersed at 20 ° C with stirring in 2 liters of softened water.
    The 2 liters of dye suspension are then placed in a kneader type kneader. 1 kg of Realglow PYG 6LLL luminescent pigment emitting in yellow / green (SrAl 2 O 4 doped Eu and Dy, particle size 400 μm) are poured in and kneaded for 3 minutes.
    After stopping the stirring, the mixture decants rapidly and the decantate is spread on shelves to a thickness of 2 to 3 cm. The shelf is then placed for 4 hours in a chamber to be heated at 50 ° C. under a stream of hot air. The pigment is then in the form of a fluid powder that is not necessary to grind. In the light of day, the pigment has the beige color of the dye. In the dark, it emits a yellow / green light identical to that of the luminescent pigment.
    The colored pigment is available to be incorporated in materials such as for example cementitious materials (mortar, concrete, screed, ...) or plastic materials (PMMA, ...), which after grinding to the desired size, can be used as aggregates in concretes.
    Examples 2 and 3: the importance of having an untreated luminescent pigment
    Two luminescent pigments A and B composed of strontium aluminate (yellow color in daylight, emitting in blue in the dark, particle size 350 μm) are used. They differ only in the fact that A is untreated whereas B has been treated with a polyethylene wax to give it better resistance to water and moisture.
    The colored pigments 2 and 3 are prepared according to the procedure of Example 1 from the compositions described in the table below:
    The pigment content of the paste is 60% by weight.
    After drying according to the same procedure as in Example 1, the colored pigment of Example 2 is in the form of a homogeneous powder of blue color in the light of day and emitting in the night blue. On the other hand, the colored pigment of Example 3 is not homogeneous, of generally less intense color, with the presence of dark blue agglomerates. This inhomogeneity is also noticeable when one looks at the light emitted in the dark by the sample 3.
    In addition, 5 g of each of these two pigments are placed under agitation in 1 liter of tap water. After about 5 minutes, stirring is stopped. The pigment 2 decants leaving the water transparent. The pigment of Example 3 decants and leaves the water colored blue, indicating that the colored luminescent pigment of Example 3 would be very sensitive to leaching problems, which is detrimental in terms of durability. The comparison of these 2 examples shows the importance of having an untreated luminescent pigment in order to achieve an effective coloration.
    Example 4: Importance of granulometry
    Untreated luminescent pigments of the same chemical composition as that of Example 2 and variable particle sizes are used. They are mixed with the same blue pigment paste and according to the same procedure as in Example 2.
    The brightness remanence is measured according to DIN 67510-1: 2009. The intensities at 10 and 60 min, as well as the extinction times (when the intensity falls below 0.3 mcd / m2). These data were measured for the luminescent pigments before staining and estimated for the colored luminescent pigment. The unit cd is the candela which is the unit of measure of the luminous intensity.
    These measurements show that it is in our interest to use pigments of large diameters, typically at least 30 μm. Indeed, for finer pigments, the remanence lasts less than one hour, which is very short, especially for the applications covered by the present invention.
    Example 5 Photoluminescence Measurement
    This measurement is carried out according to standards NF X 08-050-1 and DIN 67510-1 The objective is to measure the luminous luminance (mcd / m2) restored by a composition (C) according to the invention after exposure under an illumination produced by a Xenon bow. The sample is a material consisting of 30 parts of composite luminescent pigment according to the invention and 100 parts of PMMA.
    The luminous luminances restored after 10, 60, 90, 480 and 900 mn after the source has been stopped are given in the following table:
    The maximum luminance re-emitted by the sample after 5 minutes of illumination under 1000 lux is about 868 mcd / m2. In view of the restitution at 60 min, this places the material in Class A of NF X 08-050-1.
    The results therefore show a significant remanence of the composite pigments of the invention.
    Example 6 Characterization of Performance on Mortar
    The flexural and compressive strengths according to NF EN 196-1 and the setting time (TP) according to NF EN 480-2 of a mortar composition in which 30% of the AFNOR sand was substituted with a luminescent granulate of size 0 / 2 (average diameter between 0 and 2 mm) according to the invention. AFNOR sand is a standardized sand with a grain size between 0 and 2 mm (determined by sieving according to the requirements of EN 196-1 (2006) and ISO 679 (2009).
    Mortar composition (with afnor sand substituted at 30% by weight with a luminescent material 0/2)
    The start time (DP), end of set (FP) and total set time (TP) are grouped in the table below
    These results show that the replacement of a portion of the typical aggregates with aggregates according to the invention does not delay the setting of the hydraulic composition.
    The results of the compressive and flexural strengths are shown in the tables below.
    These results show that the replacement of a portion of the typical aggregates with aggregates according to the invention has no detrimental influence on the strengths of the mortar compositions obtained.
    Example 7 Characterization of Luminescent Pigment Size
    The particle size of a luminescent pigment obtained according to Example 1 was determined by laser granulometry (Mastersizer 2000).
    Figure 1 shows the particle size distribution in volume.
    Ordered: Volume (%)
    Abscissa: Size (pm)
    The luminescent powder has the following profile provided in FIG. 1 in a volume distribution: D10: 14.6 μm D50: 50.5 μm D90: 105.6 μm
    Example 8 Characterization of the Particle Size of Luminescent Granulants
    The granulometry of the aggregates of size 6/10 comprising 20 parts of luminescent pigment and 100 parts of PMMA was determined according to the standards NF EN 933-1 and NF EN 933-2 and is provided in FIG.
    Figure 2 is a grain size curve representing the cumulative percentage by weight of sieve (mm).
    权利要求:
    Claims (17)
    [1" id="c-fr-0001]
    A colored luminescent composite pigment comprising at least one luminescent pigment and at least one dye and having an average particle size of from about 50 to about 2000 μm.
    [2" id="c-fr-0002]
    The pigment according to claim 1, wherein the average size of the luminescent pigment particles is from about 50 to about 2000 μm, preferably from about 60 to about 2000 μm, preferably from about 60 to about 500 μm, for example between about 75 and about 200 microns.
    [3" id="c-fr-0003]
    The pigment according to claim 1 or 2, wherein the dye has a particle size of 0.1 to 10 μm.
    [4" id="c-fr-0004]
    4. A process for preparing a colored luminescent composite pigment comprising the steps of: a) providing a composition of one or more dyes as defined in claims 1 to 3 in a fluid; b) mixing with the composition of step a) at least one luminescent pigment as defined in claims 1 to 2; and c) drying the mixture obtained in step b).
    [5" id="c-fr-0005]
    5. - Process according to claim 4 comprising a step b "), before or after step c), depositing a coating on the mixture obtained in step c).
    [6" id="c-fr-0006]
    6. - colored luminescent composite pigment obtainable by the process according to claim 4 or 5.
    [7" id="c-fr-0007]
    7. - A colored luminescent composition comprising a transparent matrix and at least one colored luminescent composite pigment according to any one of claims 1 to 3 and 6.
    [8" id="c-fr-0008]
    8. - Granulate comprising a transparent matrix and at least one colored luminescent composite pigment according to any one of claims 1 to 3 and 6.
    [9" id="c-fr-0009]
    9. - Composition or granulate according to claim 7 or 8, wherein the transparent matrix is chosen from polymethyl methacrylate (PMMA), polycarbonate (PC), polyvinyl chloride (PVC), polyurethane (PU), copolymers styrene acrylonitrile (SAN) and their derivatives such as ABS (acrylonitrile / butadiene / styrene) or glass.
    [10" id="c-fr-0010]
    10. Granulate according to claim 9 for which the transparent matrix is PMMA.
    [11" id="c-fr-0011]
    11. A process for preparing a composition according to claim 7 or 9 or a granulate according to one of claims 8 to 10, comprising the steps of: 1) providing a colored luminescent composite pigment according to any one of claims 1 to 3 and 6; 2) dispersion of the composite pigment in a liquid capable of forming the transparent matrix; 3) optionally formatting the dispersion obtained in step 2), in particular in a mold; 4) optionally solidifying the mixture obtained in step 2) or 3); 5) optionally grinding the composition obtained in step 4) to obtain aggregates.
    [12" id="c-fr-0012]
    12. - The preparation method according to claim 11, comprising the step 3) shaping the dispersion obtained in step 2), in particular in a mold.
    [13" id="c-fr-0013]
    The method of claim 11 or 12 for preparing a granulate according to claim 10, comprising the steps of: 1) providing a colored luminescent composite pigment according to any one of claims 1 to 3 and 6; 2) dispersion of the composite pigment in a solution of melted PMMA; 3) shaping the dispersion obtained in step 2) in a mold, in particular using an injection molding machine; 4) solidification of the mixture obtained in step 3); 5) grinding of the composition obtained in step 4).
    [14" id="c-fr-0014]
    14. - Use of the colored luminescent composite pigment according to any one of claims 1 to 3 and 6, or a colored luminescent composition according to one of claims 7 or 9, or a granulate according to one of claims 8 to 10 in hydraulic binder compositions, plastics, varnishes and paints, coatings, coatings, inks, paper and paperboard, cosmetic compositions, glasses, ceramics, enamels, textiles, glues tiles, tile joints.
    [15" id="c-fr-0015]
    15. - Material comprising a colored luminescent composite pigment according to any one of claims 1 to 3 and 6, or a colored luminescent composition according to one of claims 7 or 9, or a granulate according to one of claims 8 to 10 , the material being preferably a hydraulic binder composition, a plastic, a varnish, a paint, a plaster, a coating, an ink, paper, cardboard, a cosmetic composition, a glass, a ceramic, an enamel, a textile, tile adhesives, tile joints.
    [16" id="c-fr-0016]
    16. A coating comprising a colored luminescent composite pigment according to any one of claims 1 to 3 and 6, or a colored luminescent composition according to one of claims 7 or 9, or a granulate according to one of claims 8 to 10. .
    [17" id="c-fr-0017]
    17. - A hydraulic binder composition, preferably concrete, comprising a colored luminescent composite pigment according to any one of claims 1 to 3 and 6, or a granulate according to one of claims 8 to 10.
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    同族专利:
    公开号 | 公开日
    FR3041651B1|2019-07-26|
    ZA201801824B|2019-08-28|
    EP3356494A1|2018-08-08|
    WO2017055531A1|2017-04-06|
    US20180346806A1|2018-12-06|
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    法律状态:
    2016-09-05| PLFP| Fee payment|Year of fee payment: 2 |
    2017-03-31| PLSC| Search report ready|Effective date: 20170331 |
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    2019-08-22| PLFP| Fee payment|Year of fee payment: 5 |
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    2021-08-11| PLFP| Fee payment|Year of fee payment: 7 |
    优先权:
    申请号 | 申请日 | 专利标题
    FR1559270|2015-09-30|
    FR1559270A|FR3041651B1|2015-09-30|2015-09-30|COLORED LUMINESCENT PIGMENT, PROCESS FOR PREPARING THE SAME AND USES THEREOF|FR1559270A| FR3041651B1|2015-09-30|2015-09-30|COLORED LUMINESCENT PIGMENT, PROCESS FOR PREPARING THE SAME AND USES THEREOF|
    PCT/EP2016/073396| WO2017055531A1|2015-09-30|2016-09-30|Coloured luminescent pigment, method for the production thereof and uses of same|
    EP16777661.6A| EP3356494A1|2015-09-30|2016-09-30|Coloured luminescent pigment, method for the production thereof and uses of same|
    US15/761,529| US20180346806A1|2015-09-30|2016-09-30|Coloured luminescent pigment, method for the production thereof and uses of same|
    ZA2018/01824A| ZA201801824B|2015-09-30|2018-03-19|Coloured luminescent pigment, method for the production thereof and uses of same|
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