9052results about How to "Uniform size" patented technology

There is provided a method of manufacturing a semiconductor device, including the following steps: flowing a first precursor gas to the semiconductor substrate within a ALD chamber to form a first discrete monolayer on the semiconductor substrate; flowing an inert purge gas to the semiconductor substrate within the ALD chamber; flowing a second precursor gas to the ALD chamber to react with the first precursor gas which has formed the first monolayer, thereby forming a first discrete compound monolayer; and flowing an inert purge gas; forming a first dielectric layer to cover the discrete compound monolayer; forming a second third monolayer above first dielectric layer; and forming a second discrete compound monolayer; and forming a second dielectric layer to cover the second discrete compound monolayer above the first dielectric layer. There is also provided a semiconductor device formed by the ALD method.

A foam composition that includes a vehicle and surface-modified nanoparticles disposed in the vehicle. The individual nanoparticles having a particle diameter of less than about 100 nanometers.

The invention provides a preparation method of graphene, and particularly relates to a method for preparing biomass graphene employing cellulose as a raw material. The specific preparation method comprises the following steps: 1, preparing a catalyst solution; 2, carrying out ionic coordination and high-temperature deoxidization on cellulose and a catalyst, so as to obtain a precursor; 3, carrying out thermal treatment; 4, carrying out acid treatment, and drying to obtain the graphene, wherein the prepared graphene is uniform in morphology, has a single-layer or multi-layer two-dimensional layered structure; the dimension is 0.5-2 microns; and the electrical conductivity is 25,000-45,000S/m. The preparation method is simple in preparation technology, low in cost, high in yield, high in production safety, and controllable in product dimension and physical property; industrialized production can be realized; the graphene prepared by the method can be applied to electrode materials of super capacitors and lithium ion batteries, and can also be added to resin and rubber as an additive; and the physical property of the material can be improved.

Provided is a chemical wet preparation method for Group 12-16 compound semiconductor nanocrystals. The method includes mixing one or more Group 12 metals or Group 12 precursors with a dispersing agent and a solvent followed by heating to obtain a Group 12 metal precursor solution; dissolving one or more Group 16 elements or Group 16 precursors in a coordinating solvent to obtain a Group 16 element precursor solution; and mixing the Group 12 metal precursors solution and the Group 16 element precursors solution to form a mixture, and then reacting the mixture to grow the semiconductor nanocrystals. The Group 12-16 compound semiconductor nanocrystals are stable and have high quantum efficiency and uniform sizes and shapes.

The invention discloses a particle-typed composite fertilizer of humic acid and manufacturing method, which consists of dressing and karyosome, wherein the dressing contains nitrogen, phosphor and potassium. The manufacturing method comprises the following steps: graining humic acid; cladding; graining; solidifying fused fertilizer on the particle of humic acid; making the composite fertilizer dissolved into water without falling; fitting for large scale of agricultural product.

Superabrasive tools and methods for the making thereof are disclosed and described. In one aspect, superabrasive particles are chemically bonded to a matrix support material according to a predetermined pattern by a braze alloy. The brazing alloy may be provided as a powder, thin sheet, or sheet of amorphous alloy. A template having a plurality of apertures arranged in a predetermined pattern may be used to place the superabrasive particles on a given substrate or matrix support material.

An electron source include a first cathode electrode disposed over a substrate and terminated to provide electrons; an emitter layer disposed over the cathode electrode and formed from one or plurality vertically aligned and mono-dispersed nano-structures that are truncated to the same length, embedded in a solid matrix and protruding above the surface for emitting electrons; an insulator disposed over the emitter layer and having one or plurality of apertures, each is self-aligned with and exposes one nano-structure in the emitter layer; and a second gate electrode disposed over the insulator, having one or plurality of apertures self-aligned with the apertures in the insulator and terminated to extract electrons from the exposed nano-structures through the apertures. The gate aperture is substantially less than one micrometer and the gated nano-structures can have a density on the order of 10⁸/cm². Such an electron source can be modulated with an extra low voltage, emits electrons with high current density and high uniformity, and operates with high energy-efficiency and long lifetime.

The invention discloses a foaming thermoplastic polyurethane bead. The foaming bead comprises 100 parts of thermoplastic polyurethane particles, 1-10 parts of cell size stabilizer, and 1-35 parts of melt viscosity modifier. The bead is prepared through the following steps: steeping the thermoplastic polyurethane particles containing a cell size stabilizer and a melt viscosity modifier in an aqueous suspension and foaming by volatilizing foaming agent. The melt viscosity of the foaming thermoplastic polyurethane bead is 8000-15000 poise below 180 DEG C, the size of the prepared foaming thermoplastic polyurethane bead is stable, the diameter of the cell is uniform, the surface is bright, the yield of the product is high, the foaming thermoplastic polyurethane bead has good sintering property even under lower vapor pressure, and the molding foam product deforms slightly and has low shrinking percentage compared with the size of the die, good dimensional stability and attractive appearance.

A system and method for sharing content among a plurality of users, enables the transfer of electronic content items captured by any of a variety of electronic content devices. The content item can include multiple levels of encoding to facilitate efficient transfer across a communication medium. The content item can be decoded at a recipient device to allow playback, display or other utilization of the content item. Content-specific encoding can be applied to enhance the transportability of the content. A content sharing application can be provided to facilitate content transfer in a computing environment, and can be implemented so as to provide an e-mail like user interface.

Composite proppant particles each of which comprises a plurality of microbubbles and a resin binder are disclosed. Also disclosed are a method of using such composite proppant particles to prop fractures in wells formed in underground formations.

The invention discloses a graphene, silver phosphate and titanium dioxide dual-functional composite and a method for preparing the same, and belongs to fields of photocatalysis technology, biological antibiosis and water pollution control. The method includes steps of ultrasonically treating oxidized graphene in water to obtain oxidized graphene dispersion liquid; dissolving silver phosphate in deionized water, adding the deionized water with the silver phosphate into the oxidized graphene dispersion liquid under the condition of stirring, and then stirring the oxidized graphene dispersion liquid to obtain mixed solution A; ultrasonically dispersing P25 in deionized water to prepare dispersion liquid, dripping the P25 dispersion liquid into the mixed solution A under the condition of magnetic stirring, and then stirring the mixed solution A to obtain mixed precursor solution B; and dripping phosphate solution into the mixed precursor solution B, then continuing stirring the mixed precursor solution B, shifting the mixed precursor solution B into a hydrothermal reaction kettle to enable the mixed precursor solution B to react so as to obtain a product, cooling the product to the room temperature, centrifuging the product, then washing the product and performing vacuum drying for the product to obtain the composite. The prepared composite not only can quickly degrade organic pollutants with certain concentration when irradiated by visible light, but also has broad-spectrum and efficient bactericidal activity for various bacteria.

The invention belongs to the technical field of recovery of lithium-ion batteries and particularly relates to a method for recovering a waste/used lithium iron phosphate positive-pole material by an acid leaching method. The method provided by the invention comprises the following steps: (a) carrying out acid leaching: adding acid into the lithium iron phosphate positive-pole material for acid leaching so as to obtain a suspension, and carrying out filtration, so as to obtain filtrate; (b) carrying out oxidation: adjusting the pH value of the filtrate obtained in the step (a) to be smaller than 1, and adding an oxidant into the filtrate to oxidate ferrous ions in the filtrate into ferric ions, so as to obtain a mixed solution; (c) carrying out separation: adjusting the pH value of the mixed solution obtained in the step (b) to be 1.5 to 4, carrying out a reaction for 1 to 3 hours at the temperature of 60 DEG C to 95 DEG C so as to produce ferric phosphate precipitates, and carrying out filtrating and washing, thereby obtaining lithium-containing filtrate and ferric phosphate. The method provided by the invention is simple in process, continuous in cycle, low in cost and easy to industrialize and is environmentally friendly; the recovery rate of Li, Fe and P reaches 95% or more, subsequent prepared FePO4 is low in impurity content, the particle size is 1 to 6 microns, is uniform and is narrow in distribution, and the morphology is controllable, so that the FePO4 is battery-grade ferric phosphate.

The invention discloses a preparation method of pellet-type formula granules. The method comprises the following steps: (1) selecting at least one of the traditional Chinese medicinal materials; (2) respectively extracting the medicinal materials selected in step (1) for obtaining extracts, or respectively grinding the medicinal materials, or respectively carrying out partial extraction and partial grinding, thus obtaining pretreated materials; and (3) preparing the pretreated materials obtained in step (2) into pellets, thus obtaining the pellet-type formula granules. According to the preparation method provided by the invention, on the basis of the prior art, the preparation process of the formula granules is innovated, the formula granules are innovated into pellets, the fluidity and moisture absorption resistance are good, the friability is small, the shape is round and uniform as well as regular, the content uniformity is small, and the divided dose is accurate.

The invention discloses low-cost green cellulose aerogel and a preparation method for hybrid aerogel thereof. The preparation method for the hybrid aerogel of the cellulose aerogel comprises the following steps that cellulose is dissolved into a zinc chloride aqueous solution, centrifugal deaeration is performed, and a uniform and transparent cellulose solution is obtained; the cellulose solution is formed, then the formed cellulose solution is placed into a coagulating bath to be regenerated, in addition, the regenerated cellulose solution is fully washed by use of a solvent, and cellulose solvent gel is obtained; the solvent in the cellulose solvent gel is removed by use of supercritical carbon dioxide drying or freeze drying, and the cellulose aerogel is obtained. Functional filler can be added into the cellulose solution to obtain the hybrid aerogel. By the adoption of different solution forming methods, the cellulose aerogel and the hybrid aerogel thereof in the shapes of sheets, fibers, particles and the like can be prepared. The preparation method is low in cost and is environmentally friendly, and the prepared aerogel is provided with a uniform nano-grade net porous structure.

An electronic device having a fingerprint verification function is provided. The electronic device includes a display; a touch recognition sensor pattern for recognizing a touch input on the display; a fingerprint recognition sensor pattern for recognizing a fingerprint input on the display; and a processor functionally connected to the display, the touch recognition sensor pattern and the fingerprint recognition sensor pattern. The processor determines whether a fingerprint recognition mode is executed, and selectively activates the touch recognition sensor pattern and the fingerprint recognition sensor pattern according to whether the determined fingerprint recognition mode is executed.

The invention discloses an efficient in-situ preparation method of a graphene reinforced copper-based composite material, and relates to a method for preparing a graphene reinforced copper-based composite material and the method can be used for solving the problems of poor uniform dispersion, poor structure integrity of grapheme and complex process in the existing preparation method of the graphene reinforced copper-based composite material. The efficient in-situ preparation method of the graphene reinforced copper-based composite material comprises the following steps: putting copper powder in a plasma reinforced chemical vapor deposition vacuum device, introducing hydrogen, preserving heat at high temperature, then introducing argon and carbon source gas, depositing, stopping introducing the carbon source gas after ending the deposition, and finally, cooling below the room temperature to obtain grapheme/copper composite powder, and then primarily pressing, sintering and secondarily pressing the grapheme/copper composite powder to obtain the graphene reinforced copper-based composite material. The method is an efficient in-situ preparation method of a graphene reinforced copper-based composite material.

The invention discloses an isatis root oil microcapsule and an isatis root oil microcapsule functional fabric finishing agent. The isatis root oil microcapsule of the invention has a particle size of 5-10 microns, and a mass ratio of a core material and a wall material of 1:0.5-1.75; the isatis root oil microcapsule functional fabric finishing agent comprises 40-65% of isatis root oil microcapsule emulsion, 5-15% of crease resistant cross-linking agents, 1.5-5% of catalysts, 0.2-2% of penetrating agents, 5-8% of softeners, and 10-35.75% of water. The isatis root oil microcapsule of the invention can cover adverse smell of isatis root oil, slowly release isatis root oil, maintain the stability of isatis root oil, and prolong its efficacy. The isatis root oil microcapsule functional fabric finishing agent of the invention provides finished fabrics with a plurality of functional effects such as durable and antibacterial effect, antiviral effect, and crease resistance, and provides fabrics with good softness and permeability.