Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K9/00—Use of pretreated ingredients
  • C08K9/02—Ingredients treated with inorganic substances
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
  • C01F17/00—Compounds of rare earth metals
  • C01F17/20—Compounds containing only rare earth metals as the metal element
  • C01F17/288—Sulfides
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
  • C01F17/00—Compounds of rare earth metals
  • C01F17/30—Compounds containing rare earth metals and at least one element other than a rare earth metal, oxygen or hydrogen, e.g. La4S3Br6
  • C01F17/38—Compounds containing rare earth metals and at least one element other than a rare earth metal, oxygen or hydrogen, e.g. La4S3Br6 sulfur being the only anion, e.g. CaLa2S4
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK  ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
  • C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK  ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
  • C09C3/00—Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
  • C09C3/06—Treatment with inorganic compounds
  • C09C3/063—Coating
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
  • C09D7/40—Additives
  • C09D7/60—Additives non-macromolecular
  • C09D7/61—Additives non-macromolecular inorganic
  • C09D7/62—Additives non-macromolecular inorganic modified by treatment with other compounds
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
  • C01P2006/00—Physical properties of inorganic compounds
  • C01P2006/60—Optical properties, e.g. expressed in CIELAB-values
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K3/00—Use of inorganic substances as compounding ingredients
  • C08K3/30—Sulfur-, selenium- or tellurium-containing compounds
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
  • Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
  • Y10T428/2991—Coated

Definitions

• the present invention relates to a composition based on a rare earth sulfide with improved chemical stability, its preparation process and its use as a pigment.
• Mineral coloring pigments are already widely used in many industries, particularly in paints, plastics and ceramics. Among these pigments are a number of compositions containing sulfur.
• products based on rare earth sulfides have already been proposed by the Applicant as substitutes for pigments comprising metals with a very high toxicity, such as, in particular, cadmium, lead, chromium and cobalt, the use of which is becoming increasingly tightly regulated.
• Compositions based on rare earth sesquisulfides and alkaline elements have thus been described in EP-A-545746.
• sulfur-based pigments generally have the drawback of releasing I ⁇ 2S in certain applications, for example during their incorporation into media such as polymers or precursors of these polymers and, in the case of l incorporation into polymers, when this is done at a relatively high temperature, for example at least 200 ° C. There is therefore a need for sulfur-based pigments whose chemical stability is improved as regards the release of H2S.
• Pigments based on rare earth sulphides and comprising a zinc compound have been developed by the Applicant and described in patent application WO 97/20002. These pigments have the property of releasing only very small amounts of H 2 S but it is necessary to further improve this property and this is therefore the object of the present invention.
• composition according to the invention is characterized in that it contains:
• the invention also relates to a process for preparing a composition of the above type which is characterized in that an attack is carried out with an acid of the surface of the aforementioned support and in that we possibly follow this attack with a neutralization.
• rare earth is understood to mean the elements of the group constituted by yttrium and the elements of the periodic classification with atomic number included inclusively between 57 and 71.
• composition according to the invention firstly comprises a support, forming a core, based on a rare earth sulfide.
• the support can be based on a rare earth sulfide of the Ln2S3 type, Ln being the rare earth, as described in EP-A-203838.
• This support can also be a rare earth and alkali sulfide. More precisely, it may be a sulfide of formula ALnS2 in which A represents at least one alkali and Ln at least one rare earth. Mention may more particularly be made of those of the following formulas: KLaS2, NaCeS2 *
• the sulfide contains at least one alkaline and / or alkaline-earth element, at least part of which is included in the crystal lattice of said sulfide.
• This sulfide can more particularly be a sesquisulfide.
• the alkaline element can be chosen in particular from lithium, sodium or potassium.
• the sulfide or sesquisulfide can comprise several alkaline or alkaline-earth elements.
• the alkaline or alkaline earth element is included at least in part in the crystal lattice of the sulfide or sesquisulfide. According to a particular embodiment, the alkaline or alkaline-earth element is included essentially or totally in the crystal lattice.
• Sesquisulfide may in particular have a cubic crystallographic structure of the Th P. ⁇ type, which has gaps in the cation network; this lacunar structure can be symbolized by giving the sesquisulfides the formula 10.66 t, 33 s 16 ( see in particular on this subject, WH ZACHARIASEN, "Crystal Chemical Studies of the 5f-Series of Elements. The Ce2S3-Ce3S4 Type of Structure" , Acta Cryst., (1949), 2, 57).
• the alkaline or alkaline-earth elements can be introduced into these cationic vacancies, until the latter are saturated or not.
• the presence of this element within the sulfide or sesquisulfide can be demonstrated by simple chemical analysis.
• X-ray diffraction analyzes show that there is conservation of the Th3P crystalline phase of sesquisulfide, with in some cases a modification more or less important mesh parameters, a function both of the nature and of the quantity of the alkaline or alkaline-earth element introduced
• the quantity of alkaline or alkaline-earth element is at most 50% of the molar quantity of rare earth of sulphide or sesquisulphide.
• the molar quantity of alkali or alkaline-earth is at least equal 0.1%, and advantageously between 5% and 50% and more particularly 5 and 20%, of the molar quantity of rare earth
• the rare earth may more particularly be the cé ⁇ um or the lanthanum. More particularly, the rare earth sesquisulfide is a cubic C ⁇ 2S3 ⁇ sesquisulfide.
• rare earth sulfides which can be used as a support in the context of the present invention, of those described in European patent application EP-A-680 930, the teaching of which is incorporated here.
• These rare earth sulfides comprise at least one element alkaline and they consist of whole monocrystalline grains of average size of at most 1.5 ⁇ m They are obtained by a process in which at least one carbonate or a hydroxycarbonate of rare earth is brought into contact with at least one compound of an element alkaline and heated in the presence of at least one gas chosen from hydrogen sulphide or carbon sulphide
• GLAS particle size generally less than 2 ⁇ m, more particularly between 0.7 and 1.5 ⁇ m After deagglomeration under mild conditions, the average size can be at most 1.5 ⁇ m and advantageously between 0.3 and 0.8 ⁇ m
• the support based on rare earth sulfide can also consist of a substrate on which the rare earth sulfide is deposited.
• This substrate can be a substrate of the mica, kaolin, silica type, titanium oxide, alumina, graphite, oxide of iron for example
• the composition comprises, in addition to the support, a layer based on at least one salt of the rare earth of the abovementioned sulphide, of a hydroxide, of an oxide of this rare earth or of 'an oxy and / or hydroxy derivative thereof
• the salt is, of course, different from the rare earth sulfide of the support.
• salt is meant a compound of the type Ln x A y where Ln represents the element rare earth and A an anion, x and y being whole numbers whose value depends on the valence and the nature of Ln and A
• Other anions can also be considered such as acetate, chloride or fluoride anions
• the layer may be based on a hydroxide or an oxide of the rare earth, that is to say a compound of formula Ln x (OH) y , or Ln x O y respectively, x and y being defined such that previously By oxy and hydroxy derivatives is meant the following compounds
• the layer may be based on one of these compounds or of a mixture of these in varying relative proportions
• a necessary condition is that the salt of the rare earth, the hydroxide, the oxide and the derivative are insoluble in water and / or in alcohols.
• insoluble is meant a solubility less than 10 ′ 5 mole / l in the solvent or the medium concerned
• This layer based on salt, hydroxide, oxide or derivative is deposited on the support and at least partially coats the latter
• This layer coating the support may not be perfectly continuous or homogeneous However, preferably, this layer is uniform and continuous
• this layer is of controlled thickness More precisely, the maximum thickness is that beyond which the rare earth sulphide thus coated would lose its pigmentary properties, generally this thickness is at most 200 nm It can more particularly be at most 100nm and preferably at most 20nm Furthermore and usually this layer is at least a few nanometers for example at least 3nm
• the continuous, homogeneous and thickness-controlled arrangement of the layer salt, hydroxide, oxide or derivative is obtained in particular when this layer comes from an acid attack of the rare earth sulfide
• the bond between the layer and the support is particularly intimate
• the composition also comprises a layer based on at least one transparent oxide, deposited on the support.
• a product of this type comprising such a layer
• this peripheral layer coating the support may not be perfectly continuous or homogeneous
• the compositions according to this variant comprise a uniform coating layer and of thickness controlled by transparent oxide, and this so as not to alter the original color of the support before coating.
• transparent oxide is meant here an oxide which, once deposited on the support in the form of a more or less fine film, absorbs little or no light rays in the visible range, and this of so as not to mask the original intrinsic color of said support, if at all.
• oxide which is used for convenience throughout the present description, should be understood as also covering hydrated type oxides. These oxides, or hydrated oxides, can be amorphous and / or crystallized. As an example of such oxides, mention may more particularly be made of silicon oxide (silica), aluminum oxide (alumina), zirconium oxide (zirconia), titanium oxide, silicate zirconium ZrSi ⁇ 4 (zircon) and rare earth oxides.
• the coating layer is based on silica or a mixture of silica and alumina.
• the composition also comprises a layer based on at least one zinc compound deposited on the support.
• This zinc compound may have been obtained by reaction of a zinc precursor with ammonia and / or an ammonium salt.
• the zinc precursor can be a zinc oxide or hydroxide which is used in suspension.
• This precursor can also be a zinc salt, preferably a soluble salt. It can be an inorganic acid salt such as a chloride, or an organic acid salt such as an acetate.
• this zinc compound thus obtained is present in the form of a zinc-ammonia complex of formula Zn (NH3) x (A) v in which A represents an anion like OH “, CI " , the acetate anion or a mixture of anions, x being at most equal to 4 and y at most equal to 2.
• the invention also comprises a third variant according to which the composition also comprises fluorine.
• the fluorine atoms are distributed according to a decreasing concentration gradient from the surface to the core of said compositions.
• the fluorine atoms are mainly distributed at the outer periphery of the compositions.
• external periphery is meant here a thickness of material measured from the surface of the particle, of the order of a few hundred Angstroms.
• We in addition means by majority that more than 50% of the fluorine atoms present in the composition are found in said external periphery
• the percentage by weight of the fluorine atoms present in the compositions does not exceed 10%, and preferably 5% - the fluorine atoms are present in the form of fluorinated or sulfofluoric compounds, in particular in the form of earth fluorides rare or rare earth sulfofluorides (thiofluorides)
• the internal layer that is to say the one closest to the support, is generally that based on salt, hydroxide, rare earth oxide or derivative or the fluorine atom layer
• the other layers can be arranged in any order It is also possible that the zinc compound, the fluorine atoms and / or the transparent oxide is present in the same layer, in a mixture, or else that these three elements even form, with the salt, the hydroxide, the rare earth oxide or the abovementioned derivative, a single single layer
• This process includes an attack with an acid on the surface of the support.
• the acid can be chosen from those capable of bringing the anion A to form the salt, the hydroxysel or the oxyhydroxysel described above. But it is also possible to work with another type of acid and in the presence of a salt capable of providing the anion A, for example ammonium sulfate which will thus provide the sulfate anion or else fluoride or ammonium chloride II is also possible to follow the acid attack with a neutralization
• This neutralization is carried out by treating the support with a base
• One can use in particular like base the products of the type hydroxides of alkalines or alkahno-earth or ammonia
• This neutralization makes it possible to obtain the compositions in which the layer comprises at least one rare earth hydroxide or a derivative of the type described above.
• this preparation comprising a neutralization, it is possible to start from acids of which rare earth salts can be soluble in water and alcohols Nitric acid can be mentioned
• the acid attack is generally carried out by suspending the support in a liquid reaction medium and then introducing the acid into this medium.
• the attack is carried out with the acid and, optionally, the neutralization , in an alcoholic medium
• This alcoholic medium can be constituted by an alcohol chosen from aliphatic alcohols such as for example butanol or ethanol
• the acid attack is carried out with an amount of acid which depends on the thickness of the layer of salt, hydroxide, oxide or derivative which it is desired to form and also on the particle size of the support.
• the acid attack can be followed by a ripening.
• the reaction medium is maintained at a constant temperature which can be for example between room temperature and 200 ° C., preferably between 20 and 100 ° C.
• the duration of the ripening is usually no more than 10 hours
• the product thus treated can be separated from the reaction medium and then dried. Drying or curing at high temperature makes it possible to obtain a layer based on rare earth oxide.
• the acid attack leads to a salt, hydroxide, oxide or derivative of a rare earth in a given oxidation state, for example a cerium hydroxide III and where there is a salt, hydroxide, oxide or derivative of this same rare earth in a higher oxidation state, for example a cerium hydroxide IV, and more insoluble in water than the species corresponding to the lower oxidation state of the rare earth, it is possible to carry out the acid attack in the presence of an oxidant such as hydrogen peroxide for example.
• an oxidant such as hydrogen peroxide for example.
• a product is thus obtained, the layer of which comprises the salt, the hydroxide, the oxide or the derivative of the rare earth in the state of superior oxidation and this product has improved stability with respect to the release of H 2 S
• a composition which also comprises a layer based on at least one transparent oxide, first the acid attack then the contact is brought into contact with a precursor of the oxy transparent and the transparent oxide is precipitated on said support
• silica In the case of silica, mention may be made of the preparation of silica by hydrolysis of an alkyl silicate, by forming a reaction medium by mixing water, alcohol, the support which is then suspended, and optionally d 'a base, an alkaline fluoride or an ammonium fluoride which can act as a catalyst for the condensation of silicate The alkyl silicate is then introduced A preparation can also be carried out by reaction of the support, a silicate, of the alkaline silicate type, and an acid
• the support, an aluminate and an acid can be reacted, whereby alumina is precipitated.
• This precipitation can also be obtained by bringing together and reacting the support, an aluminum salt and a base
• alumina can be formed by hydrolysis of an aluminum alcoholate.
• titanium oxide it can be precipitated by introducing into a hydroalcoholic suspension of the support a titanium salt on the one hand such that T1CI4, T1OCI2 or T1OSO4, and a base on the other hand
• a titanium salt on the one hand such that T1CI4, T1OCI2 or T1OSO4, and a base on the other hand
• One can also operate for example by hydrolysis of an alkyl titanate or precipitation of a titanium sol
• the acid attack is first carried out and then the said support is brought into contact, a zinc precursor, ammonia and / or an ammonium salt and the zinc compound is deposited on the support
• the zinc precursor can be a zinc oxide or hydroxide which is used in suspension.
• This precursor can also be a zinc salt, preferably a soluble salt. It can be an inorganic acid salt such as a chloride, or alternatively an organic acid salt such as acetate II is also possible to use both ammonia and an ammonium salt
• the contact between the support, the zinc precursor, the ammonia and / or the ammonium salt takes place in the presence of an alcohol.
• the alcohol used may be of the same type as that mentioned in the case of acid attack, that is to say that it is generally chosen from phatic alcohols such as, for example, butanol or ethanol
• the alcohol can, in particular, be provided with the zinc precursor under form of an alcoholic solution of zinc
• the support, the zinc precursor, the ammonia and / or the ammonium salt are brought into contact in the presence of a dispersant.
• a dispersant is to avoid agglomeration. particles forming a support during their suspension II also makes it possible to work in more concentrated media II promotes the formation of a homogeneous layer on all of the particles
• This dispersant can be chosen from the group of dispersants by stenic effect and in particular non-ionic water-soluble or organosoluble polymers. Mention may be made, as dispersing agent, of cellulose and its derivatives, polyacrylamides, polyethylene oxides, polyethylene glycols, polyoxypropylene glycols, polyoxyethylenes, polyacrylates, polyoxyethylene alkyl phenols, long chain alcohols polyoxyethylenes, polyvinyl alcohols, alkanolamides, dispersants of the polyvinylpyrrohdone type, xanthan gum-based compounds
• the fluorinating agent can be liquid, solid or gaseous.
• the operation is carried out under treatment conditions where the fluorinating agent is liquid or gaseous.
• fluorinating agents which are suitable for carrying out the treatment according to the invention, mention may more particularly be made of fluorine F2, alkali metal fluorides, ammonium fluoride, rare gas fluorides, nitrogen fluoride NF3, boron fluoride BF3, tetrafluoromethane, hydrofluoric acid HF
• fluorine F2 alkali metal fluorides, ammonium fluoride, rare gas fluorides, nitrogen fluoride NF3, boron fluoride BF3, tetrafluoromethane, hydrofluoric acid HF
• the fluorinating agent can be used pure or in dilution in a neutral gas, for example of nitrogen
• reaction conditions are preferably chosen such that said treatment only induces fluorination on the surface (mild conditions).
• degree of progress of the fluorination reaction can be monitored and monitored experimentally, for example by measuring the evolution of the mass gain of materials (mass gain induced by the progressive introduction of fluorine)
• the deposition of the transparent oxide and of the zinc compound can be carried out simultaneously by bringing the support, the precursor of the transparent oxide, the precursor of zinc and the ammonia and / or the salt
• the present invention also relates to the use as coloring pigments of the compositions described above or obtained by the above preparation processes.
• compositions or products of the invention indeed have a coloring power and a covering power and, therefore, are suitable for coloring many materials, such as plastics, paints and the like. They are very particularly suitable for plastic formulations with character acid, which can give rise to partial hydrolysis of the rare earth sulphide and / or in which they are used at a relatively high temperature Thus, and more precisely, they can be used in the coloring of polymers for plastics which can be of the thermoplastic or thermosetting type, these polymers being capable of containing traces of water.
• thermoplastic resins capable of being colored according to the invention, mention may be made, purely by way of illustration, of polyvinyl chloride, polyvinyl alcohol, polystyrene, styrene-butadiene, styrene-acrylonitrile, acrylonitrile-butadiene-styrene copolymers.
• ABS acrylic polymers, in particular polymethyl methacrylate
• polyolefins such as polyethylene, polypropylene, polybutene, polymethylpentene
• PBT polybutylene terephthalate
• cellulose derivatives such as, for example, cellulose acetate, cellulose acetate butyrate, ethylcellulose, polyamides including polyamide 6-6.
• thermosetting resins for which the compositions according to the invention are also suitable, mention may, for example, be made of phenoplasts, aminoplasts, in particular urea-formaldehyde, melamine-formaldehyde copolymers, epoxy resins and thermosetting polyesters.
• compositions of the invention can also be used in special polymers such as fluoropolymers, in particular polytetrafluoroethylene (P.T.F.E.), polycarbonates, silicone elastomers, polyimides.
• fluoropolymers in particular polytetrafluoroethylene (P.T.F.E.)
• polycarbonates in particular polytetrafluoroethylene (P.T.F.E.)
• silicone elastomers polyimides
• the compositions of the invention can be used directly in the form of powders. It is also possible, preferably, to use them in a pre-dispersed form, for example in premix with a part of the resin, in the form of a paste paste or of a liquid which allows them to be introduced at n no matter what stage of resin manufacturing.
• the products according to the invention can be incorporated into plastics such as those mentioned above in a weight proportion generally ranging either from 0.01 to 5% (reduced to the final product) or from 20 to 70% in the case of a concentrate.
• the products of the invention can also be used in the field of paints and stains and more particularly in the following resins: alkyd resins, the most common of which is called glycerophthalic; long or short oil modified resins; acrylic resins derived from esters of acrylic (methyl or ethyl) and methacrylic acid optionally copolymerized with ethyl acrylate, 2-ethylhexyl or butyl; vinyl resins such as, for example, polyvinyl acetate, polyvinyl chloride, butyralpolyvinyl, formalpolyvinyl, and copolymers of vinyl chloride and vinyl acetate or vinylidene chloride; aminoplast or phenolic resins most often modified resins, polyester resins, polyurethane resin
• the products are used at a rate of 5 to 30% by weight of the paint, and from 0.1 to 5% by weight of the stain
• the products according to the invention are also likely to be suitable for applications in the rubber industry, in particular in floor coverings, in the paper and printing ink industry, in the cosmetic field, as well as many other uses such as, for example, and not necessarily, dyes, in leathers for finishing them and laminate coverings for kitchens and other worktops, ceramics and glazes
• the products of the invention can also be used in the coloring of materials based on or obtained from at least one mineral binder
• This mineral binder can be chosen from hydraulic binders, aerial binders, plaster and binders of the anhydrous or partially hydrated calcium sulphate type.
• hydraulic binders By hydraulic binders is meant the substances having the property of setting and hardening after addition of water by forming hydrates insoluble in water.
• the products of the invention apply very particularly to the coloring of cements and of course concretes made from these cements by adding water, sand and / or gravel to them
• the cement can, for example, be of the aluminous type.
• cements based on calcium alummate, in particular those of the SECAR type Cement can also be of the silicate type and more particularly based on calcium silicate Cements may be given by way of example PORTLAND cements and, in this type of cements, the Portiand with fast or very fast setting, the white cements, those resistant to sulfates as well as those comprising slag from blast furnaces and / or fly ash and / or meta-kaolin. base of hemihydrate, calcium sulphate as well as magnesian cements known as Sorel cements
• the products of the invention are also used for coloring aerial binders, that is to say binders hardening in the open air by the action of CO2, of the calcium or magnesium oxide or hydroxide type.
• the invention is finally used for coloring plaster and binders of the anhydrous or partially hydrated calcium sulphate type (CaSU4 and CaS ⁇ 4, I / 2H2O)
• the invention relates to compositions of colored matter, in particular of the plastics, paints, stains, rubbers, ceramics, glazes, papers, inks, cosmetic products, dyes, leathers, laminated coatings or of the type based on or obtained from at least one mineral binder, which comprise, as coloring pigment, a composition according to the invention or obtained by a process of the type described above examples will now be given
• the test used to measure the emission of H 2 S is given below.
• the test measures the quantity of H 2 S released after extrusion of the pigment with polyamide 6.6 sold by Nyltech under the reference A216
• the temperature of the co-rotating twin-screw extruder is fixed at 270 ° C.
• the extrusion is carried out using a homogenized mixture containing 1484g of polymer, 15g of pigment (previously dried 4 hours at 130 ° C) and 1g of tackifier like butyl stearate
• the speed of rotation of the screws is brought to and kept equal to 120 rpm during extrusion
• the extrudate is then granulated and 400 g are placed in a one liter polyethylene bottle After 30 minutes of rest at room temperature H 2 S concentration measurements are carried out using "Drager" or "Gastec" tubes fitted with a metering pump The relative uncertainty in the measurements is 10%
• Cerium sulfide is suspended in ethanol
• the ammonium fluoride solution is then added and the mixture is stirred at ambient temperature for two hours. A fluoride treatment of the sulphide is thus carried out.
• the PVP previously dissolved in ethanol, is then added to the suspension.
• the ammonia solution is added, then the zinc in ZnO form dispersed in ethanol.
• the ethyl silicate is then introduced continuously for two hours.
• the suspension After the end of introduction of the ethyl silicate, the suspension is kept stirring for 2 hours. The particles thus obtained are washed with ethanol, then dried for 4 hours at 130 ° C.
• This example is an example according to the invention in which the support is treated with sulfu ⁇ que acid Reagents
• the cerium sulfide used is the same sulfide as that used in Example 1
• Cerium sulfide is suspended in ethanol
• cerium sulfide used is the same sulfide as that used in Example 1 In this example, neutralization is carried out using ammonia
• Cerium sulfide is suspended in water
• the sulfunque and base acid solution (ammonia N) is then added over 1.5 hours and the mixture is stirred at room temperature for 0.5 hour.
• the suspension is filtered to remove the maximum amount of water and then resuspended in ethanol
• the PVP previously dissolved in ethanol, is then added to the suspension.
• the ammonia solution (32% solution) is added, then the zinc in the form of ZnO dispersed in ethanol.
• the ethyl silicate is then introduced. continuously for two hours
• the cerium sulfide used is the same sulfide as that used in Example 1
• the acid used HERE is phosphonque acid
• Cerium sulfide is suspended in ethanol
• the phosphonque acid solution is then added over 1.5 hours and the mixture is stirred at room temperature for 0.5 hour.
• the PVP previously dissolved in ethanol, is then added to the suspension.
• the particles thus obtained are washed with ethanol, then dried for 4 h at 130 ° C.
• the cerium sulphide used is the same sulphide as that used in Example 1
• the acid used is nitric acid and neutralization is carried out with ammonia
• Cerium sulfide is suspended in ethanol
• nitric acid and base solution N ammonia
• the PVP previously dissolved in ethanol, is then added to the suspension.
• the ammonia solution (32% solution) is added, then the zinc in the form
• the suspension After the end of introduction of the ethyl silicate, the suspension is kept stirring for 2 hours. The particles thus obtained are washed with ethanol, then dried for 4 hours at 130 ° C.
• the cerium sulphide used is the same sulphide as that used in Example 1
• the acid used is nitric acid and neutralization is carried out with ammonia but in the presence of hydrogen peroxide
• the cerium sulfide is suspended in ethanol.
• the nitric acid solution and the ammonia solution are added simultaneously over 1.5 hours.
• the particles thus obtained are washed with ethanol, then dried for 4 h at 130 ° C.

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• Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)

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• 2000
  • 2000-03-30 FR FR0004062A patent/FR2807023B1/fr not_active Expired - Fee Related
• 2001
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• 2002
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