EP2376384A1 - Nanoparticules d'oxydes métalliques modifiées par des silanes - Google Patents

Nanoparticules d'oxydes métalliques modifiées par des silanes

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Publication number
EP2376384A1
EP2376384A1 EP09764257A EP09764257A EP2376384A1 EP 2376384 A1 EP2376384 A1 EP 2376384A1 EP 09764257 A EP09764257 A EP 09764257A EP 09764257 A EP09764257 A EP 09764257A EP 2376384 A1 EP2376384 A1 EP 2376384A1
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EP
European Patent Office
Prior art keywords
metal oxide
oxide particles
compound
functionalized
particles
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Application number
EP09764257A
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German (de)
English (en)
Inventor
Andrey Karpov
Hartmut Hibst
Berend Eling
Jörn DUWENHORST
Richard Riggs
Alexander Traut
Christof Kujat
Cornelia RÖGER
Christian Krausche
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BASF SE
Original Assignee
BASF SE
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Publication date
Application filed by BASF SE filed Critical BASF SE
Priority to EP09764257A priority Critical patent/EP2376384A1/fr
Publication of EP2376384A1 publication Critical patent/EP2376384A1/fr
Withdrawn legal-status Critical Current

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    • 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
    • C09C1/04—Compounds of zinc
    • C09C1/043—Zinc oxide
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B82—NANOTECHNOLOGY
    • B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G9/00—Compounds of zinc
    • C01G9/02—Oxides; Hydroxides
    • 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
    • C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
    • C09C1/36—Compounds of titanium
    • C09C1/3607—Titanium dioxide
    • C09C1/3653—Treatment with inorganic compounds
    • C09C1/3661—Coating
    • 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
    • C09C1/36—Compounds of titanium
    • C09C1/3607—Titanium dioxide
    • C09C1/3684—Treatment with organo-silicon compounds
    • 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
    • C09C1/36—Compounds of titanium
    • C09C1/3692—Combinations of treatments provided for in groups C09C1/3615 - C09C1/3684
    • 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
    • C09D7/48—Stabilisers against degradation by oxygen, light or heat
    • 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
    • C09D7/66—Additives characterised by particle size
    • C09D7/67—Particle size smaller than 100 nm
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00—Particle morphology
    • C01P2004/60—Particles characterised by their size
    • C01P2004/64—Nanometer sized, i.e. from 1-100 nanometer
    • 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
    • C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20—Oxides; Hydroxides
    • C08K3/22—Oxides; Hydroxides of metals
    • 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
    • C08K9/04—Ingredients treated with organic substances
    • C08K9/06—Ingredients treated with organic substances with silicon-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.]

Definitions

  • the invention relates to functionalized metal oxide particles, a process for their preparation and their use.
  • nanoparticulate zinc oxide with a coating of an oligo- or polyethylene glycol acid should offer improved UV protection.
  • surface-modified nanoparticulate zinc oxide should provide improved UV protection, for example in cosmetic products, with an organic acid.
  • nanoparticulate zinc oxide is surface-modified with an unsaturated organic acid and used, for example, as UV light protection filter.
  • an unsaturated organic acid for example, as UV light protection filter.
  • WO 2007/048570 A2 it is known to use two-layer surface-modified nanoparticulate zinc oxide, for example in sunscreens.
  • the acid-functionalized ZnO particles have the disadvantage that acid groups react with the ZnO surface to form metal carboxylates which are removed from the surface. This reduces effective UV protection per Zn used.
  • impurities in Zn carboxylates may have negative effects in later applications (eg, they may act as catalysts in polymerization reactions).
  • special multilayer constructions consisting of at least one ZnO-containing layer and at least one abrasion-resistant layer should have improved properties, with surface-modified nanocrystalline zinc oxide being used.
  • ZnO surface functionalization for example, 3-glycidyloxypropyltrimethoxysilane is used to obtain a colorless milky dispersion / emulsion. This haze is a drawback in a number of applications, especially where high transparency is desired.
  • DE 10 2005 010 320 B4 ZnO particles are dispersed in polar protic solvents and treated with alkoxyalkylsilanes and then treated with a UV radiation.
  • the functionalized ZnO particles should have improved properties in heterogeneous catalysis and photovoltaics. This functional However, s mecanics has the disadvantage that while relatively energy-consuming UV radiation is required. According to WO 2007/043496 A1, ZnO nanoparticles are modified with thiols or silanes and are said to offer excellent UV protection. As silane in this case 3 phenyltrimethoxysilane was used. The functionalized ZnO particles could be dispersed only after a long-term energy input, but formed no stable suspensions in methanol. Thus, such functionalized ZnO particles can only be used to a limited extent.
  • nanoparticles are obtained by reacting precursors with siloxy compounds.
  • the nanoparticles preferably contain an SiO 2 coating and / or further functionalization, inter alia organofunctional silanes.
  • this process has the disadvantage that relatively expensive bases are used for the production of nanoparticles.
  • amphiphilic silanes are used for surface modification of particles, in particular nanoparticles, inter alia of oxides or hydroxides of titanium, zinc, cerium, which are optionally used with oxides or hydroxides of silicon. These amphiphilic silanes have the disadvantage that they have at least one reactive group.
  • the invention relates to a compound F functionalized metal oxide particles having an average particle size, measured by the dynamic light scattering (DLS) method in the nano range, preferably in the range of 10 to 80 nm, in particular 10 nm to 50 nm, characterized in that Metal of the metal oxide particles is zinc, titanium or cerium or a mixture thereof and F corresponds to the following formula:
  • R 10 is C r C 4 alkyl, especially methyl or ethyl; hydrogen
  • R 11 ; R 12 is identical or different, with the meanings H, alkyl having 1 to 4 C atoms, in particular hydrogen, methyl or ethyl
  • R 1 , R 2 , R 3 are identical or different, hydrogen or alkoxy, in particular C 1 -C 4 -alkyloxy, in particular methoxy or ethyloxy; Acyloxy, in particular
  • Groups R 1 , R 2 , R 3 is hydrolyzable and in particular methoxy or
  • Sp (CH 2 ) q q is an integer, in particular 1 -10, preferably 1 -3.
  • Functionalization is understood to mean that the metal oxide particles interact with the compound F. This can be done depending on the nature of the compound F and the conditions, for example in the form of an adsorption, a coordinative bond or a chemical bond.
  • metal oxide particles refers to particles consisting essentially of metal oxide, which particles, depending on the particular environmental conditions, may also have hydroxide groups on their surface, as is known to the person skilled in the art (dissertation, B. Rohe , "Synthesis, characterization and applications of uncoated, silane-coated and UV-modified nano-zinc oxides", University of Duisburg-Essen, 2005, p. 49, 90).
  • the ZnO particles are ZnO / zinc hydroxide / zinc oxide hydrate particles.
  • fragments or products of the metal precursor can be on the metal oxide surface, for example acetate groups in the case of the use of Zn (OAc) 2 or Zn (OAc ) 2 dihydrate for the production of zinc oxide.
  • the particle size of nanoparticulate metal oxide particles a number of different methods are available to the person skilled in the art, which depend on the composition of the particles and can give partly deviating results with respect to the particle size.
  • the primary particle size can be determined by measurements using a transmission electron microscope (TEM).
  • TEM transmission electron microscope
  • the particle size correspond to the particle diameter.
  • the determination is made by dynamic light scattering (DLS).
  • the metal oxide particles FM can be doped with foreign atoms, for example with metal atoms, in particular with Fe 2+ , Fe 3+ , Co 2+ , Co 3+ , Cu 2+ , Al 3+ , In 3+ , Ga 3+ , Ni 2+ , Mg 2+ , V 5+ , Cr 3+ , Mn 2+ , Mn 4+ , Nb 5+ , Mo 5+ , Ta 5+ , La 3+ , Y 3+ , preferably in an amount of 10 to 20,000 ppm , particularly preferably from 100 to 10000 ppm (ppm refers to the number of foreign atoms in relation to the number of main metals (Zn, Ti, Ce or their both mechanical mixtures and chemical mixed oxides.)
  • the doping can be carried out in a conventional manner, for.
  • Example according to the known from DE 10 2006 035 136 A1 method of atomization of corresponding metal compounds to form an aerosol, reaction at appropriate temperatures with oxygen and workup or according to [Optical Materials, 2007, 30, pp 314-317] by a Co Precipitation and subsequent thermal treatment of solutions containing metal oxide precursors and dopant metal precursors.
  • the compound F corresponds to the formula given above with the proviso that mean:
  • R 31 , R 32 , R 33 identical or different, each an alkoxy group, in particular
  • R CH 3 O (CH 2 CHR 1 V, where R 11 is H, CH 3 or C 2 H 5 and p is an integer
  • Number of 1 to 15 means combinations of the preferred embodiments are possible.
  • Particularly preferred modifying compounds F correspond to the following formula: CH 3 O (CH 2 CH 2 O) 6-9 (CH 2 ) 3 Si (OMe) 3 , CH 3 O [CH 2 CH (CH 3 ) O] i 0 (CH 2 CH 2 O) 5 (CH 2 ) 3 Si (OEt) 3 , CH 3 O [CH 2 CH (CH 2 CH 3 ) O] 2 [CH 2 CH (CH 3 ) O] 5 (CH 2 ) 3 Si ( OEt) 3 , wherein each Et represents ethyl and Me methyl.
  • the invention further relates to a process for the preparation of functionalized metal oxide particles, characterized in that
  • the functionalization can in a conventional manner, for. In accordance with WO 2007/01 1980 A2.
  • the metal oxide particles in powder form are brought into contact with the compound F.
  • the functionalizing compound F is dissolved or dispersed in a solvent and contacted in this form with the metal oxide particles in dry form or in dispersed form.
  • the metal oxide particles and the functionalizing compound F are mixed in suitable mixing equipment, the application of high shear forces being preferred.
  • metal oxide particles and functionalizing compound F are contacted by shaking or stirring.
  • the solvents used in the functionalization are good solvents in a preferred embodiment.
  • Preferred solvents have a dielectric constant greater than 5, preferably greater than 10.
  • Particularly preferred polar solvents are water, alcohols, in particular methanol, ethanol, 1-propanol, 2-propanol, ethers, in particular tetrahydrofuran, or mixtures thereof.
  • the reaction can be carried out in the presence of a base (for example an aqueous or alcoholic ammonia solution), an acid (for example hydrochloric acid) or at least one catalyst (for example organotitanium compounds, for example tetrabutyl titanate or organotin compounds, for example dibutyltin dilaurate). favoring the hydrolysis or condensation of F.
  • the metal oxide particles can be functionalized with compound F alone or with a mixture of compound F in combination with other conventional surface functionalizing agents.
  • reaction ii) is preferably carried out at 5 to 100 0 C, in particular 40 to 70 0 C within preferably 6 minutes to 300 hours, in particular up to 72 hours.
  • the solvents and by-products specified under iv) can be added, for example, to B. by distillation, filtration (eg., By nano-, ultra- or micro-cross-filtration), centrifugation or decanting removed or replaced with other solvents.
  • the metal oxide particles furthermore contain an amorphous silicon oxygen-aluminum oxygen or zirconium oxide.
  • fabric-containing layer or their combination or mixtures preferably an amorphous SiO 2 -, Al 2 O 3 - or ZrO 2 -containing layer or their mixtures, which are applied in step iii).
  • the coatings may contain partial hydrate or hydroxy groups.
  • Such coatings are generally known to the person skilled in the art (see, for example, US Pat. Nos. 2,885,366, DE-A-159 29 51, 4,447,270, EP 449 888 B1) and are known, for example, from the deposition of hydrolyzable Si -, AI- or Zr-containing precursors available.
  • silicates, aluminates or zirconates eg sodium silicate, sodium aluminate or sodium zirconate
  • mixtures thereof are used.
  • acids eg for the SiO 2 -containing coating - silicas (for example, the ortho silicic acid H 4 SiO 4, or their condensation products, for example, disilicic H 6 Si 2 O 7 or polysilicic acids;.. For ZrO 2.
  • SiO 2 -containing coating eg metazirconic acid H 2 ZrO 3 or orthozirconic acid H 4 ZrO 4 ) or hydroxides (eg Al (OH) 3 ) or their mixtures are used, which on the hydrolysis produce SiO 2 , Al 2 O 3 or ZrO 2 or their hydrates or oxyhydroxides
  • Such precursors are known to the person skilled in the art For producing a SiO 2 -containing layer, for example tetraalkoxysilanes (US Pat.
  • Si (OR) 4 for example tetramethoxysilane, tetraethoxysilane
  • tetramethoxysilane tetraethoxysilane
  • Al-alcoholates eg aluminum isopropylate, aluminum isobutylate
  • containing layer for example Zr alcoholates (e.g. Zirconium isopropylate, zirconium n-butoxide, zirconium isobutylate).
  • an SiO 2 -containing layer is applied to the functionalized metal oxide particles.
  • the SiO 2 coating of the metal oxide particles can be carried out in a manner known per se.
  • an SiO 2 -containing layer according to EP-A 988853 can be obtained on the metal oxide particles by contacting the particles in any order with silica, water, an alkali and an organic solvent, preferably at a silicon concentration of 0.0001 to 5 moles per liter and a ratio of water to organic solvent of 0.1 to 10, especially 0.1 to 5.
  • Such a siliceous composition can be obtained, for example, by the action of water, an alkali and an organic solvent on tetraalkoxysilanes.
  • the silica can be obtained by the action of water alkali and an organic solvent on silicon tetrahalides and subsequent hydrolysis.
  • alkali are at in particular, ammonia, sodium hydroxide, potassium hydroxide carbonates or organic amines are used in the preparation of the silica.
  • the organic solvents used for the production of silica are preferably alcohols such as methanol, ethanol, propanol and pentanol, ether ketones, with ethanol being particularly preferred.
  • the SiC> 2 -containing layer can be obtained in one embodiment by dipping the metal oxide particles in the silica-containing composition.
  • the temperature for the deposition of the SiO 2 -containing layer is not critical, in a preferred embodiment it is between 10 and 100 0 C, preferably between 20 and 50 0 C.
  • the preferred pH value depends on the material to be coated. In the case of ZnO, the pH is preferably between 7 and 11.
  • the SiC> 2 coating of metal oxide particles can be carried out, for example, by hydrolysis of tetraalkoxysilanes according to WO02 / 22098-A.
  • the deposition of the polysiloxane can take place before, during or after the functionalization.
  • Preferred polysiloxanes correspond to the following formula
  • R 20 is a hydrocarbon radical, preferably an alkyl radical having 1 to 20, in particular 1 to 5 carbon atoms.
  • Preferred such polysiloxanes are pentamethoxysilane, tetraethoxysilane, tetra-n-propoxysilane, tetraisopropoxysilane and tetra-n-butoxysilane.
  • the functionalizing compounds F or tetraalkoxysilanes used for SiO 2 coating are precondensed. Such pre-condensation may take place before / during and after functionalization of the metal oxide particles. Precondensation is possible in one embodiment of the invention by introducing suitable substituents into the silanes.
  • the functionalization by reaction of the metal oxide particles with the compound F together with the SiC> 2 -containing layer forms a closed Si-C-containing layer around the metal oxide particles according to the invention.
  • a Si-C-containing layer is meant here that silicon and carbon each uniformly distributed envelop the metal oxide.
  • This closed layer is measurable and detectable by means of TEM and EDXS (Energy Dispersive X-ray spectroscopy).
  • TEM and EDXS Electrona Dispersive X-ray spectroscopy.
  • the disadvantage of the known from the prior art SiC ⁇ coating is that such particles when removing solvents can not be redispersed measured to an average particle size less than 50 nm after DLS.
  • the closed Si-C-containing layer according to the invention combines advantages of a silane functionalization and a SiC> 2 coating.
  • the UV-absorbing particles according to the invention are distinguished by the fact that they can be redispersed both in different solvents and also have a lower photocata
  • the invention further relates to a process for the preparation of UV-absorbing metal oxide particles, which are redispersible in solvent to an average particle size of less than 50 nm measured by DLS and have a Si-C-containing layer measured according to TEM and EDXS, characterized in that
  • metal oxide particles in one or more solvents are brought into contact with at least one compound F of the formula given above
  • the metal oxide particles are reacted with the compound F, if appropriate in the presence of water and optionally of a base, so that in the process a suspension an average particle size in the nano range, preferably in the range from 10 nm to 80 nm, in particular from 10 nm to 50 nm, measured according to DLS, iii) a SiO 2 -containing coating is formed by addition of an organosilane
  • polysiloxane containing exclusively hydrolyzable group or of water glass or silica and thereby the average particle size in the nano range, preferably in the range of 10 nm to 80 nm, in particular 10 nm to 50 nm measured according to DLS is iv) optionally solvent and other auxiliaries be removed.
  • UV-absorbing particles having a closed Si-C-containing layer which are redispersible in various solvents to an average particle size (% by volume) of less than 80 nm by means of dynamic light scattering are not known from the prior art.
  • the invention further relates to dispersions of UV-absorbing particles in solvents prepared by this process.
  • the invention further relates to dispersions containing the metal oxide particles according to the invention as a disperse phase, preferably in solvents as a continuous phase.
  • Solvent or solvent mixture can, for.
  • H 2 O alcohols (eg. aliphatic alcohols such as methanol, ethanol, isopropanol or aromatic alcohols such.
  • Benzyl alcohol e.g., dibutyl ether, tetrahydrofuran, dioxane
  • esters e.g., ethyl acetate, butyl acetate, propylene glycol methyl ether acetate
  • ketones e.g., acetone, methyl ethyl ketone, cyclohexanone,
  • amides e.g. Dimethylformamide, ⁇ / -methyl-2-pyrrolidone
  • hydrocarbons eg n-hexane, cyclohexane, toluene, xylene
  • the solids content of dispersions according to the invention is preferably from 0.1 to 99.9, preferably from 1 to 70, particularly preferably from 5 to 50,% by weight, based on the dispersion.
  • the dispersions according to the invention may contain further effect substances in the form of dispersed particles (eg SiC> 2 , ZrC> 2 ) or soluble molecules (eg UV absorbers, stabilizers, flameproofing agents, antioxidants, antifoggant agents, lubricants, Anti-caking agents, organic dyes, IR dyes, fluorescent dyes, brighteners, anti-static agents, biocides, nucleating agents, herbicides, fungicides or pesticides, radical scavengers).
  • dispersed particles eg SiC> 2 , ZrC> 2
  • soluble molecules eg UV absorbers, stabilizers, flameproofing agents, antioxidants, antifoggant agents, lubricants, Anti-caking agents, organic dyes, IR dyes, fluorescent dyes, brighteners, anti-static agents, biocides, nucleating agents, herbicides, fungicides or pesticides, radical scavengers.
  • modified dispersions or dry residues with other valuable additive materials such.
  • organic UV absorbers or stabilizers flame retardants are conceivable.
  • modified oxide particles may also be applied to a support (eg, polymer beads) prior to use.
  • the functionalized metal oxide particles according to the invention are suitable in the form of a dispersion or as a powder, in particular for the UV protection of polymers.
  • the functionalized metal oxide particles are contained in polymers themselves and protect them from UV radiation.
  • the functionalized metal oxide particles are contained in a polymer film or in a lacquer layer, which in turn can be used as UV protection for other materials.
  • Polymers in which the metal oxide particles according to the invention can be incorporated particularly well are, in particular, polycarbonate, polyethylene terephthalate, polyamide, polystyrene, polymethyl methacrylate and also copolymers and blends of the polymers.
  • the metal oxide particles according to the invention can be introduced into a polymer for UV protection in a manner known per se, for example using an extruder or kneader.
  • the polymers can also be dispersions of the polymers, for example in the case of paints or coatings. obligations.
  • the incorporation can be done by conventional mixing operations.
  • the functionalized metal oxide particles according to the invention and dispersions containing them are also particularly suitable for coating surfaces, for example of wood, plastics, fibers or glass, as well as for coatings, paints and coatings.
  • the metal oxide particles and dispersions according to the invention are also suitable for use as UV protection in cosmetic preparations and sunscreens.
  • they can preferably be used in an amount of 1 to 50, preferably 5 to 30 wt .-%, based on the preparation.
  • the measurements are carried out with a device from Malvern Instruments at room temperature.
  • the average particle size is determined by the volume fraction.
  • the TEM investigations were carried out on a device Tecnai G2 from Fa. FEI with an integrated Energy Dispersive X-ray Spectroscopy (EDXS).
  • the samples were prepared on a C-hole film (Lacey Carbon Film). Element analysis using EXDS was done at those spots where the film had a hole.
  • the white residue of ZnO modified with 2- [methoxy (polyethyleneoxy) propyl] trimethoxysilane prepared according to Example 2 was redispersed after removal of 2-propanol and NH 3 in 38 g of DMF.
  • the mean particle size determined by DLS was 26 nm.
  • Example 5 The white residue of ZnO modified with 2- [methoxy (polyethyleneoxy) propyl] trimethoxysilane prepared according to Example 2 was redispersed after removal of 2-propanol and NH 3 in 38 g of THF. The mean particle size determined by DLS was 23 nm. The TEM measurement confirmed a primary particle size of about 10 nm.
  • Example 5 The white residue of ZnO modified with 2- [methoxy (polyethyleneoxy) propyl] trimethoxysilane prepared according to Example 2 was redispersed after removal of 2-propanol and NH 3 in 38 g of THF. The mean particle size determined by DLS was 23 nm. The TEM measurement confirmed a primary particle size of about 10 nm. Example 5
  • the white residue of ZnO modified with 2- [methoxy (polyethyleneoxy) propyl] trimethoxysilane prepared according to Example 2 was redispersed after removal of 2-propanol and NH 3 in 38 g of cyclohexanone.
  • the mean particle size determined by DLS was 18 nm.
  • Dispersion comprising ZnO modified with 2- [methoxy (polyethyleneoxy) propyl] trimethoxysilane in water
  • the white residue of ZnO modified with 2- [methoxy (polyethyleneoxy) propyl] trimethoxysilane prepared according to Example 2 was redispersed after removal of 2-propanol and NH 3 in 38 g of water.
  • the mean particle size determined by DLS was 18 nm.
  • Dispersion comprising ZnO modified with 2- [methoxy (polyethyleneoxy) propyl] trimethoxysilane and subsequently coated with SiC> 2 in water
  • the white residue of ZnO modified with 2- [methoxy (polyethyleneoxy) propyl] trimethoxysilane prepared according to Example 7 was redispersed after removal of 2-propanol and NH 3 in 38 g of water.
  • the average particle size determined by DLS was 45 nm.
  • the TEM measurement confirmed a primary ZnO particle size of about 10 nm.
  • EDXS Energy Dispersive X-ray Spectroscopy
  • the white residue of ZnO modified with 2- [methoxy (polyethyleneoxy) propyl] trimethoxysilane prepared according to Example 7 was redispersed after removal of 2-propanol and NH 3 in 38 g of cyclohexanone.
  • the mean particle size determined by DLS was 34 nm.

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Abstract

L'invention concerne des nanoparticules d'oxyde métallique améliorées, notamment de l'oxyde de zinc, modifiées par des silanes. Les particules ainsi obtenues conviennent pour assurer une meilleure protection des polymères contre les UV.
EP09764257A 2008-12-12 2009-12-03 Nanoparticules d'oxydes métalliques modifiées par des silanes Withdrawn EP2376384A1 (fr)

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EP09764257A EP2376384A1 (fr) 2008-12-12 2009-12-03 Nanoparticules d'oxydes métalliques modifiées par des silanes

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EP08171437 2008-12-12
EP09764257A EP2376384A1 (fr) 2008-12-12 2009-12-03 Nanoparticules d'oxydes métalliques modifiées par des silanes
PCT/EP2009/066351 WO2010066640A1 (fr) 2008-12-12 2009-12-03 Nanoparticules d'oxydes métalliques modifiées par des silanes

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EP2376564A2 (fr) 2008-12-12 2011-10-19 Basf Se Dispersions contenant des nanoparticules fonctionnalisées de type oxyde
EP2449155A1 (fr) 2009-06-30 2012-05-09 Basf Se Fibres de polyamide à particules pouvant être colorées et procédé de fabrication associé
WO2011023266A1 (fr) * 2009-08-28 2011-03-03 Basf Se Nanoparticules modifiées
WO2011061132A1 (fr) * 2009-11-20 2011-05-26 Basf Se Catalyseur multicouche utilisé pour la production d'acides carboxyliques et/ou d'anhydrides d'acide carboxylique, à l'antimoniate de vanadium dans au moins une couche de catalyseur, et procédé de production d'anhydride d'acide phtalique à basse température en zone de surchauffe maximale
WO2011073120A1 (fr) 2009-12-17 2011-06-23 Basf Se Matériau de support d'oxyde de métal contenant des particules métalliques du groupe fer-platine à l'échelle nanométrique
US20110230668A1 (en) * 2010-03-19 2011-09-22 Basf Se Catalyst for gas phase oxidations based on low-sulfur and low-calcium titanium dioxide
US8901320B2 (en) 2010-04-13 2014-12-02 Basf Se Process for controlling a gas phase oxidation reactor for preparation of phthalic anhydride
US8859459B2 (en) 2010-06-30 2014-10-14 Basf Se Multilayer catalyst for preparing phthalic anhydride and process for preparing phthalic anhydride
US20120010112A1 (en) 2010-07-06 2012-01-12 Basf Se Acid-free quaternized nitrogen compounds and use thereof as additives in fuels and lubricants
US9212157B2 (en) 2010-07-30 2015-12-15 Basf Se Catalyst for the oxidation of o-xylene and/or naphthalene to phthalic anhydride
JP5874436B2 (ja) * 2012-02-22 2016-03-02 堺化学工業株式会社 酸化亜鉛粒子及びその製造方法
US20150159036A1 (en) * 2013-12-11 2015-06-11 Momentive Performance Materials Inc. Stable primer formulations and coatings with nano dispersion of modified metal oxides
GB201409208D0 (en) * 2014-05-23 2014-07-09 Tioxide Europe Ltd Titanium dioxide
TW201703879A (zh) 2015-06-02 2017-02-01 西克帕控股有限公司 用於生產光學效應層之製程
CN109071258B (zh) * 2016-03-31 2020-12-29 日产化学工业株式会社 结合有两亲性有机硅烷化合物的无机氧化物微粒、其有机溶剂分散液以及被膜形成用组合物
DE102016209499A1 (de) * 2016-05-31 2017-11-30 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Nanostrukturierte Mikropartikel aus silanisierten Primärpartikeln mit steuerbarer Redispergierbarkeit und Verfahren zu deren Herstellung

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