Abstract:
A rinse solution for a silica thin film includes trimethylbenzene, diethylbenzene, indane, indene, tert-butyl toluene, methylnaphthalene, a mixture including an aromatic hydrocarbon having 12 or more carbon atoms, a mixture including an aliphatic hydrocarbon having 12 or more carbon atoms, a mixture including a hetero hydrocarbon compound including a phenyl group and an oxygen atom, or a combination thereof.
Abstract:
A process for preparing a mesoporous material, e.g., transition metal oxide, sulfide, selenide or telluride, Lanthanide metal oxide, sulfide, selenide or telluride, a post-transition metal oxide, sulfide, selenide or telluride and metalloid oxide, sulfide, selenide or telluride. The process comprises providing an acidic mixture comprising a metal precursor, an interface modifier, a hydrotropic or lyotropic ion precursor, and a surfactant; and heating the acidic mixture at a temperature and for a period of time sufficient to form the mesoporous material. A mesoporous material prepared by the above process. A method of controlling nano-sized wall crystallinity and mesoporosity in mesoporous materials. The method comprises providing an acidic mixture comprising a metal precursor, an interface modifier, a hydrotropic or lyotropic ion precursor, and a surfactant; and heating the acidic mixture at a temperature and for a period of time sufficient to control nano-sized wall crystallinity and mesoporosity in the mesoporous material. Mesoporous materials and a method of tuning structural properties of mesoporous materials.
Abstract:
Provided is a silicon oxide for an anode of a secondary battery, having a good mechanical lifespan and electrical properties, and a method for preparing the same and an anode of a secondary battery using the silicon oxide. According to the method, a mixture is prepared by mixing SiCl4 and ethylene glycol, a gel is manufactured by stirring the mixture, and the gel is heat treated to prepare silicon oxide for an anode of a secondary battery.
Abstract:
Disclosed are silica nanoparticles that are suitable as templates for preparing membranes of controlled pore sizes and pore arrangements. The silica nanoparticles have a density of about 1.96 g/cm3 or less. Also disclosed is a method of preparing such nanoparticles which involves reacting an orthosilicate and an alcohol or a mixture of alcohols in an aqueous medium in the presence of a salt of the metal or a metalloid compound, optionally in combination with ammonium hydroxide, isolating the resulting nanoparticles, and treating the resulting particles with an acid.
Abstract:
Provided are methods of preparing silica particles having two maximum values in number particle size distribution, wherein in the two maximum values, a particle size ratio (a maximum value of a small-size side/a maximum value of a large-size side) between a maximum value of a large-size side and a maximum value of a small-size side is from 0.02 to 0.3, and a number ratio (a number of silica particles having a maximum value of the small-size side/number of silica particles having a maximum value of the large-size side) is from 1 to 100, and particles within a range of 10% from the large-size side of the silica particles have an average circularity of from 0.65 to 0.90 and an average shrinkage ratio of from 10 to 50.
Abstract:
The present invention is directed to a method of making metal oxide and mixed metal oxide particles. The method includes treating a mixture formed from a metal source, such as metal alkoxide, a surfactant, and a first alcohol in an aqueous media at a very high metal oxide yield. The mixture is reacted using a catalyst to form metal oxide particles having a desired particle size in said mixture. By washing the particles with an aprotic solvent, the residual carbon content of the particles can be significantly reduced. The method is particularly suitable for forming silica particles. The metal oxide particles can then be heat treated to form synthetic fused metal oxides such as, for example, synthetic fused silica.
Abstract:
Cubic mesoporous silicas having substantially cylindrical morphology may be prepared using a combination of a first structure-directing template, such as tetramethyl ammonium hydroxide; water; a second structure-directing template, such as cetyltrimethylammonium bromide; a morphology-directing template, such as a poloxamer having a weight average molecular weight ranging from 5,000 to 20,000 Daltons; and a silica source; in the substantial absence of an alcohol solvent. The resulting materials may exhibit a three-dimensional channel structure, a length from 3 to 10 micrometers and a width from 300 nanometers to 10 micrometers, resulting in an aspect ratio from 1 to 300. Further characterization may include a surface area from 1300 to 1500 square meters per gram, an average pore diameter from 20 to 26 angstroms, and an average pore volume ranging from 0.7 to 1.1 cubic centimeters per gram. These materials are useful for molecular transport and release applications in a variety of uses, including, for example, membrane separations, metal incorporation, electronic devices, drug delivery, and adsorption.
Abstract:
The synthetic amorphous silica powder of the present invention is characterized in that it comprises a synthetic amorphous silica powder obtained by applying a spheroidizing treatment to a silica powder, and by subsequently cleaning and drying it so that the synthetic amorphous silica powder has an average particle diameter D50 of 10 to 2,000 μm; wherein the synthetic amorphous silica powder has: a quotient of 1.00 to 1.35 obtained by dividing a BET specific surface area of the powder by a theoretical specific surface area calculated from the average particle diameter D50; a real density of 2.10 to 2.20 g/cm3; an intra-particulate porosity of 0 to 0.05; a circularity of 0.75 to 1.00; and an unmolten ratio of 0.00 to 0.25.
Abstract:
This disclosure relates to a water repellent and oil repellent film including microprojections having a specific shape and size on the surface, an electrical and electronic apparatus including the film, and an electrical and electronic apparatus including an outer surface on which microprojections having a specific shape and size are formed.
Abstract:
A method for synthesizing silica nanofibers using sound waves is provided. The method includes providing a solution of polyvinyl pyrrolidone, adding sodium citrate and ammonium hydroxide to form a first mixture, adding a silica-based compound to the solution to form a second mixture, and sonicating the second mixture to synthesize a plurality of silica nanofibers having an average cross-sectional diameter of less than 70 nm and having a length on the order of at least several hundred microns. The method can be performed without heating or electrospinning, and instead includes less energy intensive strategies that can be scaled up to an industrial scale. The resulting nanofibers can achieve a decreased mean diameter over conventional fibers. The decreased diameter generally increases the tensile strength of the silica nanofibers, as defects and contaminations decrease with the decreasing diameter.