7458 results about "Silicic acid" patented technology

The present invention relates to the atomic layer deposition (“ALD”) of high k dielectric layers of metal silicates, including hafnium silicate. More particularly, the present invention relates to the ALD formation of metal silicates using metal organic precursors, silicon organic precursors and ozone. Preferably, the metal organic precursor is a metal alkyl amide and the silicon organic precursor is a silicon alkyl amide.

[Problem]

A microbial pesticidal composition containing viable spores of a bacterium belonging to the genus Bacillus and a chemical pesticide, in which the spores can be preserved stably in a living state for a long period of time, and a method for preserving the spores stably in a living state for a long period of time, are provided.

[Dissolution Means]

Viable spores of Bacillus subtilis and/or Bacillus amyloliquefaciens are blended with at least one member selected from a metal oxide, a metal hydroxide, a metal oxide silicic acid salt, and a metal hydroxide silicic acid salt.

The invention relates to a preparation method of a super-hydrophobic cellulose material with a micro-nano structure. The method comprises the following steps: (1) adding ethyl orthosilicate and functionalized siloxane into an ethanol system containing deionized water to obtain a dispersion liquid of functionalized silica particles A in the presence of ammonium hydroxide serving as a catalyst; with the dispersion liquid of functionalized silica particles A as seeds, sequentially adding the ethyl orthosilicate, the functionalized siloxane, the deionized water, the ammonium hydroxide and the ethanol so as to obtain a dispersion liquid of functionalized silica particles B; (2) performing ultrasonic dispersion on the two types of functionalized silica particles in dimethylformamide, then adding a hydrophobic polymer and a low surface energy additive into the system and evenly stirring so as to form white dispersion liquid; and (3) coating the white dispersion liquid obtained in the step (2) on a natural cellulose material in a direct spraying manner or a spin coating manner so as to obtain the super-hydrophobic cellulose material with the micro-nano structure. The coating material has strong scouring resistance and acid-alkali resistance besides the excellent hydrophobic property.

The invention discloses a preparation method for a Beta zeolite molecular sieve with a hierarchical porous structure. Ethyl orthosilicate is used as a silicon source, sodium metaaluminate is used as an aluminum source, hexaammonio cationic quaternary ammonium surfactant is used as a template, and then the hierarchical porous zeolite molecular sieve containing meso pores and Beta zeolite micropores is prepared by using a hydro-thermal synthesis process under an alkaline condition. According to the invention, the hexaammonio cationic quaternary ammonium surfactant is used as a Beta zeolite structure guiding agent and generates micropores, aggregation of hydrophobic long-chain alkyl groups on the surfactant forms the meso pores, so the prepared Beta zeolite molecular sieve has both meso pores and the crystalline micropores. The structure with both the meso pores and the micropores enables defects of a single pore structure to be avoided and mass transfer efficiency to be improved, and the Beta zeolite molecular sieve has a wide application prospect in aspects of macro-molecular catalysis, adsorption, separation, etc.

Disclosed is a surface treating agent for metallic materials that has various properties such as corrosion resistance and overcoating properties and, when used in coating-type surface treatment, particularly can form a film , which has excellent adhesion to the surface of metallic materials, and can fix, within the film, a component capable of functioning as a corrosion inhibitor for metallic materials. The surface treating agent for metallic materials comprises a silicic acid compound (A), an organoalkoxysilane (B), a metallic compound (C) containing at least one metal element selected from the group consisting of Zr, Ti, Co, Fe, V, Ce, Mo, Mn, Mg, Al, Ni, Ca, W, Nb, Cr, and Zn, at least one compound (D) selected from the group consisting of phosphoric acid compounds and fluoro compounds, water (E), and an alcohol (F) produced upon hydrolysis of the organoalkoxysilan (B). The molar concentration (mol/L) of the alcohol (F) in the treating agent has been regulated in a predetermined range.

The invention relates to a liquid silicon fertilizer and a production technique thereof, and belongs to the technical field of fertilizer. The liquid silicon fertilizer is characterized in that raw materials comprise soluble silicon, urea, trace elements, chelate and fulvic acid, which are prepared into the balanced compound fertilizer. The production technique comprises the following steps: 1, dissolving solid potassium metasilicate; 2, dissolving sulfate of the trace elements in water, and adding EDTA into the mixture to obtain the chelate of the EDTA trace elements; and adding boric acid, ammonium molybdate, the urea and the fulvic acid into the mixture after cooling and filtration; and 3, blending the chelate into the mixture to obtain the liquid silicon fertilizer. The production technique is characterized in that (1) the production technique uses water glass and the fulvic acid chelate, has better buffer action for alkali, and can effectively improve stability of SiO3; and (2) the trace elements are chelated twice by using the EDTA and the fulvic acid to form chelated metal ions, so as to prevent silicic acid radicals and the metal ions reacting to form silicate difficult to be dissolved in water, and influence utilization rate of silicon element. The production technique uses the liquid potassium metasilicate and large amount of elements, trace elements and organic substances to establish a balanced compound system, and can effectively improve utilization rate of the silicon element and various nutrient elements for the crops.

The present invention discloses a method for preparing low density silica aerogel under normal pressure. The method comprises: mixing tetraethoxysilane, water and ethanol according to a volume ratio of 1:0.5-19:1-29, adding an acid to adjust the pH value to 3-4, carrying out catalysis hydrolysis, adding an alkali to adjust the pH value to 6-6.5, carrying out catalysis gelating for 8-10 min to obtain a wet gel, aging the wet gel for 6-36 h at a room temperature, adding n-hexane to carry out solvent replacement for 6-36 h, immersing in a trimethylchlorosilane and n-hexane mixed solution to carry out hydrophobic modification for 12-15 h, adopting a n-hexane washing solution to remove the modification solution, placing into a muffle furnace to heat to a temperature of 30-250 DEG C, drying, and finally cooling to a room temperature to obtain the silica aerogel. Test results show that the density of the SiO2 aerogel is 50-80 kg/m<3> and is significantly lower than the density of the SiO2 aerogel prepared under the normal pressure dry condition in most of the public reports.

The invention discloses an organic-inorganic hybrid super-hydrophilic coating as well as a preparation method and an application thereof. The preparation method comprises: firstly carrying out hydrolysis condensation polymerization by a sol-gel method with ethyl orthosilicate used as a precursor, hydrochloric acid used as a catalyst, ethanol used as a solvent, a silane coupling agent used as a modifier and a proper amount of water to obtain a modified silica sol, then carrying out free radical polymerization on the modified silica sol and reactive hydrophilic monomers to obtain an organic-inorganic hybrid material, and carrying out solvent replacement to obtain an aqueous organic-inorganic hybrid super-hydrophilic coating. The coating is coated on plastics, glass or metal substrates through dipping or brushing to form a coating layer, the coating layer has a contact angle with water less than 5 degrees, the adhesion force with the substrates of level-0 and the hardness greater than 6H, and water drops can spread out quickly on the coating layer.

The present invention relates to an air-drying silane coating composition containing an epoxy or acrylic resin, an optional silicic ester or alkyl silicate, an aminoalkylsilane component, an optional organoalkyoxysilane, and possible auxiliaries; methods of use thereof, and articles and substrates coated accordingly.

The invention relates to organic-inorganic hybrid ultraviolet cured paint for metal surface protection. The paint comprises the following components in percentage by weight: 10 to 25 percent of epoxy modified silicon dioxide gel-resin, 15 to 30 percent of bisphenol-A epoxy acrylic ester, 5 to 15 percent of urethane acrylate, 35 to 45 percent of reactive diluent, 2 to 5 percent of toughener, 4 to 6 percent of photoinitiator, 0.5 to 0 percent of addition agent, wherein the epoxy modified silicon dioxide gel-resin is prepared by hydrolyzing a mixture of ethyl orthosilicate and gamma-glycidoxy propyl trimethoxy silane by a sol-gel method first and then adding diethylenetriamine. The paint film formed after the curing of paint has good strength, hardness, flexibility and strong acid and base resistance. The invention solves the problems that the organic-inorganic hybrid paint has high requirement on curing and common ultraviolet cured paint has poor adhesive force and flexibility when cured on metal base materials.

The invention provides a preparation method of a silicon dioxide super-hydrophobic thin film. The preparation method comprises the following steps of: step one. preparing alkaline colloidal sol, namely mixing orthosilicate ester, a basic catalyst, a solvent and water to prepare the SiO2 alkaline colloidal sol; step two. adding hexamethyl disilazane to the SiO2 alkaline colloidal sol for reaction to obtain modified SiO colloidal sol; and step three. coating the modified SiO colloidal sol on the surface of a substrate, and drying to obtain the silicon dioxide super-hydrophobic thin film. The invention also provides a super-hydrophobic material. The silicon dioxide super-hydrophobic thin film prepared by the method has strong adhesion force with a substrate and a good dewatering effect; complicated equipment is not needed; the process is simple; the preparation cycle is shortened; the cost is saved; and the application range is wide.

The invention relates to a SiO2 aerogel/inorganic cotton compound thermal insulation felt and a preparation method of the SiO2 aerogel/inorganic cotton compound thermal insulation felt. The method comprises the following steps of: compounding silica sol and inorganic cotton; ageing the silica sol and the inorganic cotton; carrying out modification and solvent replacement processing; and drying at normal pressure to obtain the SiO2 aerogel/inorganic cotton compound thermal insulation felt. The preparation method of the SiO2 aerogel/inorganic cotton compound thermal insulation felt, which is disclosed by the invention, is characterized in that cheap and easily-obtained industrial raw materials, such as industrial sodium silicate, industrial silica sol, glass wool, rock wool and mineral wool are adopted, the production cost can be lowered, and the ordinary pressure drying technology is convenient and easy to realize, is simple to operate and is suitable for large-scale industrial production. Meanwhile, the product is nontoxic and harmless and does not pollute the environment.

The preparation method for high specific capacity and specific power manganous ferrous lithium silicate with formula as Li2MSiO4(M=Mn(1-x)Fex, 0íœxíœ1)/C as anode material for lithium cell comprises: mixing the lithium salt, manganous salt, ferrite and normal silicate ester into water-alcohol system, heating to obtain the mixed predecessor; then, grinding with sugar to mix and treat at high-temperature in nitrogen. Wherein, there is 84~97% silicate and 3~16% carbon. This invention is simple and convenient to operate, and has high performance-price ratio.

The invention discloses a nanosilicon dioxide modified polyurethane elastomer and a preparation method thereof. The preparation method comprises the steps of enabling polyether glycol, isocyanate and micromolecular dihydroxy alcohol to be subjected to addition polymerization reaction to prepare a polyurethane prepolymer as a component A; uniformly mixing a chain extender, ethyl silicate and a silane coupling agent, carrying out in-situ hydrolysis on ethyl silicate to form nanosilicon dioxide particles, performing surface hydrophobicity modification on the nanosilicon dioxide particles by using the silane coupling agent, and removing a solvent in the mixture to obtain a component B; uniformly mixing the component A and the component B according to a certain ratio, degassing, pouring and carrying out vulcanization molding to obtain the nano-modified polyurethane elastomer. By using the preparation method, the uniform dispersion of silicon dioxide particles in polyurethane is realized, the enhancement effect of nanoparticles is sufficiently taken, the prepared polyurethane elastomer is obtained by crosslinking the nanosilicon dioxide particles, and the heat resistance and chemical stability of the polyurethane elastomer can be remarkably improved; in addition, the nanosilicon dioxide modified polyurethane elastomer can meet the requirements of a sealing element for mechanical strength, wear resistance, high elasticity and oil resistance and has a wide market prospect.

Hydrolysable and polymerizable or polyadditive silanes and methods of their production and the production of (hetero)silicic acid polycondensates or of polymers. The silanes in accordance with the invention are of general formulain which the groups and indices are equal or different and have the following meaning:R=hydrogen, R2-R1-R4-SiXxR33-x, carbonyl, alkyl, alkenyl, aryl, alkylaryl or arylalkyl;R1=alkylene, arylene, arylenealkene or alkenearylene;R2=alkylene, arylene, arylenealkene or alkenearylene;R3=Alkyl, alkenyl, aryl, alkylaryl or arylalkyl;R4=-(CHR6-CHR6)n-, where n=0 or 1, -CHR6-CHR6-S-R5-; -CO-S-R5-, -CHR6-CHR6-NR6R5-, -Y-CS-NH-R5-, -S-R5-, -Y-CO-NH-R5-, -CO-O-R5-, -Y-CO-C2H3(COOH)-R5-, -Y-CO-C2H3(OH)-R5- or -CO-NR6-R5-;R5=alkene, arylene, arylenealkene or alkenearylene;R6=hydrogen, alkyl or aryl with 1 to 10 carbon atoms;R9=hydrogen, alkyl, alkene, aryl, alkylaryl or arylalkyl;X=hydrogen, halogen, hydroxy, alkoxy, acyloxy, alkylcarbonyl, alkoxycarbonyl or NR''2, where R''=hydrogen, alkyl or aryl;Y=-O-, -S- or -NR6-;Z=-O- or -(CHR6)m-, where m=1 or 2;a=1, 2 or 3, with b=1 for a=2 or 3;b=1, 2 or 3, with a=1 for b=2 or 3;c=1 to 6;x=1, 2 or 3;a+x=2, 3 or 4.

The invention relates to magnetic silicon dioxide microspheres with a nuclear shell and surface anisotropic double functional groups and a preparation method thereof. The preparation method comprises the following steps of: preparing superparamagetic microspheres by a solvothermal process; preparing magnetic microspheres which are coated by silicon dioxide by a sol-gel process; preparing the magnetic silicon dioxide microspheres of which the surface has amino group by taking the magnetic silicon dioxide microspheres as seeds and by the copolycondensation of alkyl ester orthosilicate and a silane coupling agent, and drying the magnetic silicon dioxide microspheres to obtain samples; and by a PICKERING emulsion technology, stabilizing a paraffin/aqueous emulsion system with a micrometer scale by using the aminated magnetic microspheres to form single-layer close packing of the magnetic microspheres on the surface of paraffin spheres, then reacting the amino group on the surface of the magnetic microspheres which is exposed in a liquid phase with succinic anhydride to introduce carboxyl into the partial surface of the microspheres, so that the surfaces of the magnetic microspheres have the anisotropic double functional groups. The obtained magnetic microspheres with the double functional groups have the advantages that: magnetic responsiveness is high; grain size can be controlled between 200 and 800 namometers; and the density of the surface functional groups can be adjusted.

A method of manufacturing a colloidal silica dispersion, by dissolving a fumed silica in an aqueous solvent having an alkali metal hydroxide to produce an alkaline silicate solution; removing the alkali metal via ion exchange to produce a silicic acid solution; adjusting the temperature, concentration and pH of the silicic acid solution to values sufficient to initiate nucleation and particle growth at elevated temperatures; and cooling the silicic acid solution at a rate sufficient to produce the colloidal silica dispersion. The colloidal silica particles in the colloidal silica dispersion have a mean particle size about 2 nm to about 100 nm. Also provided is a method of chemical mechanical polishing a surface of a substrate by contacting the substrate and a composition having a plurality of colloidal silica particles according to the present invention and a medium for suspending the particles. The contacting is carried out at a temperature and for a period of time sufficient to planarize the substrate.

The invention discloses Lyophobic and oleophylic micro nano-coatings applied to oil filtering dehydration and a preparation method thereof. Base material of the coatings is metal mesh grid with 50-1800 meshes, the surface of the metal mesh grid is coated with a layer of dense micro nano-coating which is dense thin film composed of nano silica global particles with partical size ranging from 90nm to 500nm.In the method of the invention, the sol-gel method is adopted, tetraethyl ester serves as the precursor, ammonia water serves as the catalyst, ethanol serves as the solvent, alkyl oxosilane serves as lyophobic modifier, the method of hydrolytie polycondensation is adopted to obtain lyophobic nano silica sol, the process of impregnation or spraying is adopted to coat the gel on the metal mesh grid with 50-1800 meshes, after thermal treatment, oil-water separation net with lyophobic and oleophylic properties is obtained. The method of the invention features simple process, no harm to the environment, no need of fluorine material, wide application to coalescing separator as a separation filter element and the function of filtration and dehydration of oil.