1130results about How to "Control concentration" patented technology

Apparatus and method for forming a polycrystalline silicon thin film by converting an amorphous silicon thin film into the polycrystalline silicon thin film using a metal are provided. The method includes: a metal nucleus adsorbing step of introducing a vapor phase metal compound into a process space where the glass substrate having the amorphous silicon formed thereon is disposed, to adsorb a metal nucleus contained in the metal compound into the amorphous silicon layer; a metal nucleus distribution region-forming step of forming a community region including a plurality of silicon particles every metal nucleus in a plane boundary region occupied by the metal compound by a self-limited mechanism due to the adsorption of the metal nucleus; and an excess gas removing step of purging and removing an excess gas which is not adsorbed in the metal nucleus distribution region-forming step.

The invention discloses a control method for aerosol in flue gas desulfurization by utilizing an ammonia method and a master desulfurizing tower, and the control method is characterized in that flue gas enters the master desulfurizing tower after being cooled to the relative humidity of 90 to 100% and the temperature of 60 to 80 DEG C through high-pressure waster mist or prewashing temperature reduction; the generation of the aerosol particles in the desulfurization by utilizing the ammonia method is reduced by optimizing desulfurization operating conditions, and the formed aerosol particles are condensed to grow big and are partially washed to be eliminated through a desulfurizing solution; an appropriate amount of steam is injected into the saturated flue gas through desulfurizing and eliminating the partial aerosol particles; the oversaturated water vapor environment required by the secondary condensation and the growth of the aerosol particles is established on the top of the master desulfurizing tower; and the condensed and the grown aerosol particles are eliminated through a high-efficiency demister. The invention combines the formation mechanism of the aerosol in the flue gas desulfurization by utilizing the ammonia method; and the formation of the aerosol is reduced by optimizing the process conditions of the desulfurization operation and the elimination of the formed aerosol is promoted by utilizing a steam phase change principle at the same time so that the exhaust problem of the aerosol in the flue gas desulfurization by utilizing the ammonia method can be effectively solved.

The invention provides a medical anti-sticking membrane and a preparation method thereof. The anti-sticking membrane comprises a nanometer frame and hydrosol attached thereon. The hydrosol is internally packed with one or several kinds of styptic medicament or/and anti-sticking medicament. The invention also provides a preparation method of the anti-sticking membrane, comprising the following steps of: preparing electro-spinning solution, styptic medicament and/or anti-sticking medicament-containing hydrosol solution and crosslinker solution; receiving static spinning with the crosslinker solution to obtain the nanometer frame; printing the styptic medicament and/or anti-sticking medicament-containing hydrosol solution onto the nanometer frame by an ink-jet printer, and solidifying the hydrosol solution to obtain the anti-sticking membrane. The anti-sticking membrane has good capability and biological compatibility, and nontoxicity as well as nonirritant, can be completely degraded and absorbed, is compounded with controllably released styptic medicament or/and anti-sticking medicament, has controllable degrading time and speed, and conquers defects of the prior art.

The invention provides a novel indoor air purification device. Water or an aqueous solution is used for absorbing various types of gas and granular pollution components in air, so that the aim of purifying the air is fulfilled; a Venturi throat opening is formed in an air channel; when the gas passes through the throat opening, the speed of gas flow is obviously increased, and high shearing force is formed in the gas flow, so that liquid entering the Venturi throat opening is sheared into extremely thin fog drops; after leaving the Venturi throat opening, the gas flow is slowed down and forms strong turbulent fluctuation, so that particles in the air and the extremely thin water drops can be in full contact and collision, and the particles in the air are transferred into liquid; the water drops in a turbulent fluctuation region also collide, and the water drops are re-enlarged, so that the water drops can be removed from a gas-liquid separation chamber, and the gas pollution components in the air are dissolved in the liquid so as to be absorbed and removed.

Improved taste masking of pharmaceutical compositions of unpleasant-tasting drugs and cyclodextrin is achieved by forming a mixture of drug and cyclodextrin wherein the drug's dissolution rate has been retarded, or the the cyclodextrin's dissolution rate has been enhanced, or by both.

A solid-state image sensor includes, in each pixel, a p-type well provided on a semiconductor substrate, a photodiode provided in the p-type well, a transfer gate for transferring photocharges accumulated in the photodiode, and an n-type diffusion region for receiving the transferred photocharges. The photodiode includes a first n-type accumulation region, and a second n-type accumulation region having a concentration higher than that of the first accumulation region and provided at a position deeper than the first accumulation region. The first accumulation region extends toward an end of the transfer gate, and the second accumulation region is separate from the transfer gate.

A method and a device to increase the efficiency of dialysis for the removal from blood of substances that are more or less tightly bound to carriers such as albumin. According to the invention this is accomplished by a simultaneous significant increase of the flow rate of the dialysis fluid and of the area of the membrane that separates the blood from the dialysis fluid, compared to conventional dialysis.

The invention relates to a positive electrode material of a high-capacity dynamic-type nickel-rich lithium ion battery and a preparation method. The molecular formula of the positive electrode material of the high-capacity dynamic-type nickel-rich lithium ion battery is LiaNi1-x(MM')xO2.M''O, wherein a is equal to 0.9-1.2, x is more than or equal to 0 and less than or equal to 0.7, and M is at least one of Co, Mn and Al; M' is at least one of Co, Al, V, Mn, Zr, Mg, Ti, Cr, Zr, La, Ce, Pr, Nd, Nb, Mo, Y, Sr, Ba, B, Sr, Sn and Ta; M''O is a cladding layer, and M'' is Co and Al. The invention also relates to a preparation method for the positive electrode material of the high-capacity dynamic-type nickel-rich lithium ion battery. The material machining performance is excellent, the battery prepared by utilizing the material, the cycling performance and the high-voltage performance are excellent, the safety and stability in use can be realized, not only can the application performance requirement of a portable electronic device on the battery be met, but also the positive electrode material is applicable to the power battery.

The invention relates to a preparation method of 1,4-butanediol diglycidyl ether cross-linked sodium hyaluronate gel. The method comprises the steps of: by taking high-concentration sodium hyaluronate solution as reaction matrix, performing first cross-linking for a longer time under the low-temperature condition by adding less cross-linking agent, then performing secondary deep cross-linking under high-temperature condition, and finally processing and pelleting through short-time dialysis technique, thereby obtaining the sodium hyaluronate gel product. With the method, the cross-linking condition of the high-concentration cross-linking agent under the traditional high-temperature condition can be eliminated, milder secondary depth cross-linking condition is adopted, the reaction efficiency of the less cross-linking agent can be greatly improved, the residual cross-linking agent is more easily removed, and the excellent biocompatibility of the cross-linked sodium hyaluronate gel can be ensured. The method is simple in preparation technique, excellent in controllability and easier to practically produce on large scale.

An optoelectronic device includes at least first and second light-emitting nanowires on a support, each comprising an area for the injection of holes and an area for the injection of electrons, a series electric connection including a connection nanowire on the support, which includes a first region forming an electric path with the hole injection area of the first nanowire, a second region forming an electric path with the electron injection area of the second nanowire, and a third region enabling a current to flow between first and second regions. Also included are a first conductive area connecting the hole injection area of the first nanowire and the first region of the connection nanowire and electrically insulated from the second nanowire, and a second conductive area connecting the second region of the connection nanowire and electron injection area of the second nanowire and electrically insulated from the first nanowire.

An object of the present invention is to obtain, with respect to a semiconductor light-emitting element using a group III nitride semiconductor substrate, a semiconductor light-emitting element having an excellent light extraction property by selecting a specific substrate dopant and controlling the concentration thereof. The semiconductor light-emitting element comprises a substrate composed of a group III nitride semiconductor comprising germanium (Ge) as a dopant, an n-type semiconductor layer composed of a group III nitride semiconductor formed on the substrate, an active layer composed of a group III nitride semiconductor formed on the n-type semiconductor layer, and a p-type semiconductor layer composed of a group III nitride semiconductor formed on the active layer in which the substrate has a germanium (Ge) concentration of 2×10¹⁷ to 2×10¹⁹ cm⁻³. The substrate is produced in a nitrogen-containing atmosphere using a melt comprising at least a group III element, an alkali or alkaline earth metal, and germanium (Ge) and nitrogen.

The invention relates to a benthonic animal-algae-aquatic plant-fish based river water ecological environment self-remediation method. The method is to overcome problems of river water ecological environment remediation methods at present, namely short effect duration, high costs and easy generation of secondary pollution. The method includes 1) evaluating the degree of pollution of a river, 2) planting reed and seeding algae, 3) throwing in plankton and benthic mollusks, 4) planting submerged plants, 5) throwing in shrimps, herbivorous fishes, omnivore fishes and filter-feeding fishes, 6) throwing in carnivorous fishes, and 7) harvesting the reed and the submerged plants before the reed and the submerged plants die, catching the benthic mollusks and the shrimps, and catching the fishes after two years. The method is long in effect duration, low in cost and free of secondary pollution and is applied for the field of river water pollution remediation.

The invention discloses a method for synthesizing polycarboxylate superplasticizer through a RAFT method. According to the method, firstly, macro-monomers A are added into a reaction kettle, water is added, water bath heating is performed till the temperature is 65-85 DEG C, and constant-temperature stirring is performed; then, a trithio ester chain transferring agent is dissolved in a mixed solution of micro-monomers B and water, the mixture is dropwise added into the reaction kettle at constant speed, and meanwhile an initiator aqueous solution is dropwise added; after all the needed matter is dropwise added, a stirring reaction lasts for 3-5 h under the continuous constant-temperature stirring condition of 65-85 DEG C; after the reaction ends, an alkali solution and water are added to adjust PH to 6-7, and the polycarboxylate superplasticizer is obtained after reaction products are cooled to room temperature. By means of the method, the molecular-structure-controllable polycarboxylate superplasticizer can be prepared, the molecular weight is controllable, the molecular weight distribution range is narrow, polymer molecule design can also be performed, and the method has great significance in research and development of the polycarboxylate superplasticizer synthetic technology.

The invention discloses an evaluation device for coal-fired flue gas pollutant sorbent, which includes a simulation flue gas steel bottle carrying pollutant, a gas steel bottle carrying mercury, a mercury vapor generator, mass flowmeters A and B, a gas mixing tank, a two-way valve, a mercury state converting device, a mercury analyzer, a computer, a tail gas processing device and a fixed bed, wherein in the bed body of the fixed bed, glass beads with the particle size of 0.5 to 2mm or hard polyester material can be adopted as bed material, sorbent with the particle size of 0.5 to 1.5mm is dispersed in the bed material, and the mass ratio of the bed material to the sorbent in the fixed bed is 50-70:1. Through the adoption of the evaluation device for the coal-fired flue gas pollutant sorbent, provided by the invention, related pollutant entering the fixed bed such as SO2, NOx and HgO can be absorbed by the sorbent in the fixed bed at a certain temperature, so as to control the pollutant; meanwhile, the adsorption effect of the sorbent can be evaluated conveniently and quickly.

The invention relates to a method and a system for refining crude brine. The method comprises the following steps of: performing pre-reaction; pressurizing and dissolving gas; pretreating; performing post reaction; filtering by using a membrane; and filtering off residual slag particles by using a membrane filter to obtain the refined brine. By the method and the system for refining crude brine, under the condition of not introducing new impurities, various metal impurity ions are efficiently flocculated and precipitated, so that problems of great mineral salt impurity fluctuation and overproof Fe and Al ions are solved, the high quality of the finished brine product and the high-efficiency and normal operation of subsequent ion-exchange membrane electrolysis can be ensured, and the aim that mineral salt replaces sea salt to serve as chlor-alkali electrolysis raw salt is fulfilled; moreover, brine sludge emission and treatment cost can be obviously reduced, and the method and the system have good emission reduction effect and good environment-friendly property.

The invention discloses a manufacturing method of an R-Fe-B sintered magnet. The manufacturing method of the R-Fe-B sintered magnet comprises the main steps of preparing a R1-Fe-B-M sintered magnet as a matrix; arranging an RLO particle layer of light rare earth element on the surface of the matrix and arranging a heavy rare earth RHX which comprises either dysprosium metal, or dysprosium hydride or both the dysprosium metal and the dysprosium hydride on the RLO particle layer; performing heating treatment inside a sintering furnace to enable the heavy rare earth RHX to evaporate to the surface of matrix by penetrating through the RLO particle layer and to diffuse from the surface to the inside of the magnet, wherein during the whole process, the RLO particle layer serves as transmission media and does not react with heavy rare earth elements. According to the manufacturing method of the R-Fe-B sintered magnet, the RLO particle layer of oxide and fluoride of light rare earth element is arranged between the magnet and the heavy rare earth RHX, so that on the one hand, non-direct contact of the magnet and the heavy rare earth RHX is achieved, on the other hand, the diffusion process of heavy rare earth RHX steam can be inhibited and slowed down, and excessive evaporation of the heavy rare earth RHX steam to the surface of the magnet can be prevented.

A transistor includes a substrate, an active region including a source region, a channel region, and a drain region which are crystallized using an SGS crystallization method and are formed on the substrate so that a grain size of a first annealed portion and a second annealed portion are different from each other, a gate insulating layer formed on the active region, and a gate electrode formed on the gate insulating layer.

Endovascular devices are provided. The endovascular devices include a conformable scaffold with one or more outpocketings. The outpocketing in the endovascular device creates a corresponding outpocketing of a vessel wall, thereby altering local fluid dynamics.

The invention discloses a diamond grinding wheel for cutting a silicon crystal circle and a preparation method thereof. The method comprises the following steps: (1) preprocessing an aluminum alloy basal body; (2) configuring electroforming liquid: configuring the electroforming liquid according to the weight ratio of (38-43):(15-20):(43-57):(50-180):(4-8) of nickel sulphate, cobalt sulphate, deionized water, a diamond grinding material and a suspending agent; fully stirring evenly and obtaining the electroforming liquid; (3) carrying out insulation processing on the aluminum alloy basal body obtained in the step (1), putting the aluminum alloy basal body into the electroforming liquid, electroforming in an ultrasonic field, evenly precipitating the diamond grinding material in the electroforming liquid and metal on the basal body together and obtaining a grinding wheel blank body with a compound electroforming layer; and (4) taking out the grinding wheel blank body completing electroforming, and carrying out accurate processing on the grinding wheel blank body on a numerical control grinder and a numerical control lathe respectively according to the accuracy requirements of the required basal body and the required cutting edge. The diamond grinding wheel obtained by the invention meets the ultrathin and superfine technical conditions and also has favorable strength and rigidity.

A nitride semiconductor laser diode includes a substrate, an n-side nitride semiconductor layer formed on the substrate, an active layer formed on the n-side nitride semiconductor layer and having a light emitting layer including In_xAl_yGa_1−x−yN (0<x<1, 0 y<1, 0<x+y<1), and a p-side nitride semiconductor layer formed on the active layer. In the nitride semiconductor laser diode, the lasing wavelength of the nitride semiconductor laser diode is 500 nm or greater, dislocations originated in the active layer penetrate through the p-side nitride semiconductor layer, with the dislocation density in the p-side nitride semiconductor layer being 1×10⁶ cm⁻² or greater, and the concentration distribution of p-type impuritys in the depth direction is such that, from the light emitting layer toward the surface of the p-side nitride semiconductor layer, the concentration of the p-type impurity reaches a maximum value of 5×10¹⁸ cm⁻³ or greater within a range of 300 nm from the top portion of the light emitting layer which is closest to the p-side nitride semiconductor layer, and after reaching the maximum value, the concentration remains at 6×10¹⁷ cm⁻³ or greater in the above-described range of 300 nm.

The invention discloses a hepatic targeted temperature sensitive microsphere and a preparation method therefor, and belongs to the functional polymer material field, and especially relates to a drug sustained release and targeted drug delivery material and a preparation method therefor. The temperature response range of the material is 25 DEG C-37 DEG C, and the particle size of the microsphere is about 500nm. The microsphere can be prepared through the following method: glycyrrhetinic acid (GA) is modified by ethylene diamine and acrylic acid (AAc) and vinyl monomers are generated; ammonium persulfate (APS) is employed as an initiator, N,N-methylene bisacrylamide (MBA) is employed as a cross-linking agent, hepatic targeted temperature sensitive microspheres are prepared through a semicontinuous soap-free emulsion polymerization method. The preparation method has simple technological processes, and mild experiment conditions, needs no special devices, has a low investment cost, and has good operability. The reagents are all common reagents. The reaction residues are easy to remove. The preparation method is convenient for industrial implementation.

We have developed an improved vapor-phase deposition method and apparatus for the application of films/coatings on substrates. The method provides for the addition of a precise amount of each of the reactants to be consumed in a single reaction step of the coating formation process. In addition to the control over the amount of reactants added to the process chamber, the present invention requires precise control over the total pressure (which is less than atmospheric pressure) in the process chamber, the partial vapor pressure of each vaporous component present in the process chamber, the substrate temperature, and typically the temperature of a major processing surface within said process chamber. Control over this combination of variables determines a number of the characteristics of a film/coating or multi-layered film/coating formed using the method. By varying these process parameters, the roughness and the thickness of the films/coatings produced can be controlled.

The present invention relates to a new process for producing methane chloride by using liquid-phase catalytic method and pressurization process. The hydrogen chloride and methyl alcohol are mixed according to a certain ratio, then placed in a tank reactor with catalyst, and under the condition of a certain temp. and pressure the invented methane chloride can be synthesized. It adopts acid/water washing and alkali-washing processes to remove unreacted methyl alcohol and hydrogen chloride, and adopts concentrated sulfuric acid washing process to remove residual water content and reaction by-product dimethyl ether, then the purified and dried methane chloride gas is undergone the processes of compression and condensation so as to obtain high-purity liquid methane chloride product.