490results about "Titanium oxides/hydroxides" patented technology

A fast quench reaction includes a reactor chamber having a high temperature heating means such as a plasma torch at its inlet and a restrictive convergent-divergent nozzle at its outlet end. Reactants are injected into the reactor chamber. The resulting heated gaseous stream is then rapidly cooled by passage through the nozzle. This "freezes" the desired end product(s) in the heated equilibrium reaction stage.

Disclosed is a method of exfoliating a layered material (e.g., graphite and graphite oxide) to produce nano-scaled platelets having a thickness smaller than 100 nm, typically smaller than 10 nm, and often between 0.34 nm and 1.02 nm. The method comprises: (a) subjecting the layered material in a powder form to a halogen vapor at a first temperature above the melting point or sublimation point of the halogen at a sufficient vapor pressure and for a duration of time sufficient to cause the halogen molecules to penetrate an interlayer space of the layered material, forming a stable halogen-intercalated compound; and (b) heating the halogen-intercalated compound at a second temperature above the boiling point of the halogen, allowing halogen atoms or molecules residing in the interlayer space to exfoliate the layered material to produce the platelets. Alternatively, rather than heating, step (a) is followed by a step of dispersing the halogen-intercalated compound in a liquid medium which is subjected to ultrasonication for exfoliating the halogen-intercalated compound to produce the platelets, which are dispersed in the liquid medium. The halogen can be readily captured and re-used, thereby significantly reducing the impact of halogen to the environment. The method can further include a step of dispersing the platelets in a polymer or monomer solution or suspension as a precursor step to nanocomposite fabrication.

Doped, pyrogenically prepared oxides of metals and / or non-metals which are doped with one or more doping components in an amount of 0.00001 to 20 wt. %. The doping component may be a metal and / or non-metal or an oxide and / or a salt of a metal and / or a non-metal. The BET surface area of the doped oxide may be between 5 and 600 m2 / g. The doped pyrogenically prepared oxides of metals and / or non-metals are prepared by adding an aerosol which contains an aqueous solution of a metal and / or non-metal to the gas mixture during the flame hydrolysis of vaporizable compounds of metals and / or non-metals.

Synthesis process for new particles of Li4Ti5O12, Li(4-alpha)ZalphaTi5O12 or Li4ZbetaTi(5-beta)O12, preferably having a spinel structure, wherein beta is greater than 0 and less than or equal to 0.5 (preferably having a spinel structure), alpha representing a number greater than zero and less than or equal to 0.33, Z representing a source of at least one metal, preferably chosen from the group made up of Mg, Nb, Al, Zr, Ni, Co. These particles coated with a layer of carbon notably exhibit electrochemical properties that are particularly interesting as components of anodes and / or cathodes in electrochemical generators.

Mesoscopically ordered, hydrothermally stable metal oxide-block copolymer composite or mesoporous materials are described herein that are formed by using amphiphilic block polymers which act as structure directing agents for the metal oxide in a self-assembling system.

A process of treating metal oxide nanoparticles that includes mixing metal oxide nanoparticles, a solvent, and a surface treatment agent that is preferably a silane or siloxane is described. The treated metal oxide nanoparticles are rendered hydrophobic by the surface treatment agent being surface attached thereto, and are preferably dispersed in a hydrophobic aromatic polymer binder of a charge transport layer of a photoreceptor, whereby π—π interactions can be formed between the organic moieties on the surface of the nanoparticles and the aromatic components of the binder polymer to achieve a stable dispersion of the nanoparticles in the polymer that is substantially free of large sized agglomerations.

Silicon-titanium mixed oxide powder prepared by flame hydrolysis, having a ratio by weight of silicon dioxide / titanium dioxide, which is greater on the surface of the primary particles than that within the total primary particle. It is prepared by a flame hydrolysis process, in that a stream consisting of a vaporous titanium dioxide precursor and oxygen or an oxygen-containing gas and hydrogen, and a second stream consisting of a vaporous silicon dioxide precursor and a carrier gas consisting of oxygen, an oxygen-containing gas and / or an inert gas, are guided separately into the reaction chamber of a burner such as is known for the preparation of pyrogenic oxides, and are burnt here, the solid mixed oxide powder and hot gases are subsequently cooled, and the gases are separated from the solid. The powder may be used, for example, for the preparation of sunscreen preparations.

A method for administration of a substance into the dermis of a mammal is disclosed. The method involves administration into the dermis by injection which results in improved systemic absorption relative to that obtained upon subcutaneous administration of the substance. The substance administered may be a growth hormone, a low molecular weight heparin or a dopamine receptor agonist.

A process to produce mixed metal oxides and metal oxide compounds. The process includes evaporating a feed solution that contains at least two metal salts to form an intermediate. The evaporation is conducted at a temperature above the boiling point of the feed solution but below the temperature where there is significant crystal growth or below the calcination temperature of the intermediate. The intermediate is calcined, optionally in the presence of an oxidizing agent, to form the desired oxides. The calcined material can be milled and dispersed to yield individual particles of controllable size and narrow size distribution.

Methods are described that have the capability of producing submicron / nanoscale particles, in some embodiments dispersible, at high production rates. In some embodiments, the methods result in the production of particles with an average diameter less than about 75 nanometers that are produced at a rate of at least about 35 grams per hour. In other embodiments, the particles are highly uniform. These methods can be used to form particle collections and / or powder coatings. Powder coatings and corresponding methods are described based on the deposition of highly uniform submicron / nanoscale particles.

Synthesis process for new particles of Li4Ti5O12, Li(4-α)ZαTi5O12 or Li4ZβTi(5-β)O12, preferably having a spinel structure, wherein β is greater than 0 and less than or equal to 0.5 (preferably having a spinel structure), α representing a number greater than zero and less than or equal to 0.33, Z representing a source of at least one metal, preferably chosen from the group made up of Mg, Nb, Al, Zr, Ni, Co. These particles coated with a layer of carbon notably exhibit electrochemical properties that are particularly interesting as components of anodes and / or cathodes in electrochemical generators.

Nanoparticles comprising titanium, such as nanoscale doped titanium metal compounds, inorganic titanium compounds, and organic titanium compounds, their methods of manufacture, and methods of preparation of products from nanoparticles comprising titanium are provided.

Nanoparticles comprising titanium, such as nanoscale doped titanium metal compounds, inorganic titanium compounds, and organic titanium compounds, their methods of manufacture, and methods of preparation of products from nanoparticles comprising titanium are provided.

The invention relates to a method for modification of a biocompatible component comprising the steps of a) providing a biocompatible component at least partly covered by metallic oxide; and b) treating at least a part of said component, which part is covered by said metallic oxide, with an aqueous composition comprising oxalic acid; whereby a modified metallic oxide is obtained. The invention also relates to a biocompatible component comprising a substrate having a surface comprising a) a microstructure comprising pits separated by plateus and / or ridges; and b) a primary nanostructure being superimposed on said microstructure, said primary nanostructure comprising depressions arranged in a wave-like formation.

A low-temperature hydrothermal reaction is provided to generate crystalline perovskite nanotubes such as barium titanate (BaTiO3) and strontium titanate (SrTiO3) that have an outer diameter from about 1 nm to about 500 nm and a length from about 10 nm to about 10 micron. The low-temperature hydrothermal reaction includes the use of a metal oxide nanotube structural template, i.e., precursor. These titanate nanotubes have been characterized by means of X-ray diffraction and transmission electron microscopy, coupled with energy dispersive X-ray analysis and selected area electron diffraction (SAED).

A technique for bonding an organic group with the surface of fine particles such as nanoparticles through strong linkage is provided, whereas such fine particles are attracting attention as materials essential for development of high-tech products because of various unique excellent characteristics and functions thereof. Organically modified metal oxide fine particles can be obtained by adapting high-temperature, high-pressure water as a reaction field to bond an organic matter with the surface of metal oxide fine particles through strong linkage. The use of the same condition enables not only the formation of metal oxide fine particles but also the organic modification of the formed fine particles. The resulting organically modified metal oxide fine particles exhibit excellent properties, characteristics and functions.

Untargeted magnetic nanoparticles exhibiting collective behavior and enhanced heating ability in thermotherapeutic applications are described, as are methods for using such untargeted magnetic nanoparticles.

The present invention is directed to novel sol-gel methods in which metal oxide precursor and an alcohol-based solution are mixed to form a reaction mixture that is then allowed to react to produce nanosized metal oxide particles. The methods of the present invention are more suitable for preparing nanosized metal oxide than are previously-described sol-gel methods. The present invention can provide for nanosized metal oxide particles more efficiently than the previously-described sol-gel methods by permitting higher concentrations of metal oxide precursor to be employed in the reaction mixture. The foregoing is provided by careful control of the pH conditions during synthesis and by ensuring that the pH is maintained at a value of about 7 or higher.

The present invention relates to nanoconjugates. In particular, the present invention provides nanoconjugates for diagnostic (e.g., imaging), research, and clinical (e.g., targeted treatment) applications.

A method for synthesis of high quality colloidal nanoparticles using comprises a high heating rate process. Irradiation of single mode, high power, microwave is a particularly well suited technique to realize high quality semiconductor nanoparticles. The use of microwave radiation effectively automates the synthesis, and more importantly, permits the use of a continuous flow microwave reactor for commercial preparation of the high quality colloidal nanoparticles.

A positive electrode active material includes: a particle including a lithium composite oxide; a first layer that is provided on a surface of the particle and includes a lithium composite oxide; and a second layer that is provided on a surface of the first layer. The lithium composite oxide included in the particle and the lithium composite oxide included in the first layer have the same composition or almost the same composition, the second layer includes an oxide or a fluoride, and the lithium composite oxide included in the first layer has lower crystallinity than the lithium composite oxide included in the particle.

Potassium titanate is obtained which has a novel configuration, exhibits excellent wear resistance when incorporated in a friction material and shows an excellent reinforcement performance when incorporated in a resin composition. A manufacturing method of the potassium titanate, a friction material using the potassium titanate and a resin composition using the potassium titanate are also obtained. The potassium titanate is represented by K2TinO(2n+1) (n=4.0-11.0) and has the highest X-ray diffraction intensity peak (2θ) in the range of 11.0°-13.5° with its half width being not less than 0.5°.

The invention provides a hydrothermal synthesis method for IVB-group metal oxide. The IVB-group metal oxide is the oxide of titanium, zirconium or hafnium. The method comprises: adding IVB-group metal salt solution to alkaline precipitant and obtaining hydroxide precipitate; washing and precipitating to remove other impurities; adding water to the hydroxide precipitate to prepare suspension liquid and then performing hydrothermal reaction to obtain metal-oxide suspension liquid; and performing post-treatment to the metal-oxide suspension liquid to obtain metal oxide powder. The hydrothermal synthesis method can form zirconia powder through reaction at low temperature, thereby overcoming the disadvantage of using a co-precipitation method to product zirconia, avoiding powder agglomeration caused by high-temperature calcinations, ensuring the extremely excellent performance of the obtained zirconia powder and having the advantages of uniform particle size, good dispersity, strong maneuverability and the like. According to the hydrothermal synthesis method, zirconia composite material can also be produced by further adding stabilizers, such as yttrium-oxide compound zirconia, magnesium-oxide compound zirconia, cerium-oxide compound zirconia, calcium-oxide compound zirconia and the like.

Fine core / shell composite particles comprising fine inorganic nanometer-size particles as cores and a fluoropolymer having units derived from a fluoromonomer as shells, their production method and their application are provided. The fine composite particles of the present invention are fine composite particles comprising fine inorganic nanometer-size particles, the surface of which is covered with a fluoropolymer having units derived from a fluoromonomer, wherein the proportion of the fine inorganic particles is from 1 to 90 mass %, and the fluoropolymer is a fluoropolymer having units derived from a fluoromonomer having a polymerizable unsaturated group in which a carbon atom has a fluorine atom bonded thereto. The method for producing fine composite particles of the present invention is a method for producing the above fine composite particles, which comprises polymerizing the above fluoromonomer by seed polymerization in a polymerization system wherein fine inorganic nanometer-size particles are dispersed in an aqueous medium in the presence of a surfactant. A powder comprising the above fine composite particles is useful as a bulking agent to be blended with a thermoplastic polymer or a thermosetting resin, and a thermoplastic polymer or a thermosetting resin containing the fine composite particles is used as a molding material. Further, a powder of the fine composite particles in which the proportion of the fine inorganic particles is low can be used by itself as a molding material.

A crystal which can be employed as the active material of a lithium-based battery has an empirical formula of Lix1A2Ni1-y-zCoyBzOa, wherein “x1” is greater than about 0.1 and equal to or less than about 1.3, “x2,”“y” and “z” each is greater than about 0.0 and equal to or less than about 0.2, “a” is greater than about 1.5 and less than about 2.1, “A” is at least one element selected from the group consisting of barium, magnesium, calcium and strontium and “B” is at least one element selected from the group consisting of boron, aluminum, gallium, manganese, titanium, vanadium and zirconium. A method includes combining lithium, nickel, cobalt and at least one element “A” selected from the group consisting of barium, magnesium, calcium and strontium, has at least one element “B” selected from the group consisting of boron, aluminum, gallium, manganese, titanium, vanadium and zirconium, in the presence of oxygen, wherein the combined components have the relative ratio of Lix1:Ax2:Ni1-y-z:Coy:Bz, wherein “x1,”“x2,”“y” and “z” have the values given for the empirical formula shown above.

To provide an aluminum magnesium titanate crystal structure which can be used stably in variable high temperatures, because of its excellent heat resistance, thermal shock resistance, high thermal decomposition resistance and high mechanical property, and a process for its production. An aluminum magnesium titanate crystal structure, which is a solid solution wherein at least some of Al atoms in the surface layer of aluminum magnesium titanate crystal represented by the empirical formula MgxAl2(1−x)Ti(1+x)O5 (wherein 0.1≦x<1) are substituted with Si atoms, and which has a thermal expansion coefficient of from −6×10−6 (1 / K) to 6×10−6 (1 / K) in a range of from 50 is to 800° C. at a temperature raising rate of 20° C. / min, and a remaining ratio of aluminum magnesium titanate of at least 50%, when held in an atmosphere of 1,100° C. for 300 hours.