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219results about How to "Improve particle size uniformity" patented technology

Nickel-manganese composite hydroxide particles, method for producing same, positive electrode active material for nonaqueous electrolyte secondary batteries, method for producing said positive electrode active material, and nonaqueous electrolyte secondary battery

Provided are nickel manganese composite hydroxide particles that are a precursor for forming cathode active material comprising lithium nickel manganese composite oxide having hollow structure of particles having a small and uniform particle size for obtaining a non-aqueous electrolyte secondary battery having high capacity, high output and good cyclability. When obtaining the nickel manganese composite hydroxide particles from a crystallization reaction, an aqueous solution for nucleation, which includes at least a metallic compound that contains nickel and a metallic compound that contains manganese, and does not include a complex ion formation agent that forms complex ions with nickel, manganese and cobalt, is controlled so that the temperature of the solution is 60 DEG C or greater, and so that the pH value that is measured at a standard solution temperature of 25 DEG C is 11.5 to 13.5, and after nucleation is performed, an aqueous solution for particle growth, which includes the nuclei that were formed in the nucleation step and does not substantially include a complex ion formation agent that forms complex ions with nickel, manganese and cobalt, is controlled so that the temperature of the solution is 60 DEG C or greater, and so that the pH value that is measured at a standard solution temperature of 25 DEG C is 9.5 to 11.5, and is less than the pH value in the nucleation step.
Owner:SUMITOMO METAL MINING CO LTD

Nickel composite hydroxide and process for producing same, positive active material for nonaqueous-electrolyte secondary battery and process for producing same, and nonaqueous-electrolyte secondary battery

To provide a positive active material which has a moderate particle diameter and has high evenness in particle diameter and a nickel composite hydroxide which is for use as a precursor for the positive active material. When a nickel composite hydroxide is obtained through a crystallization reaction, an aqueous solution for nucleation which contains both a metal compound at least containing nickel and an ammonium ion source is used to conduct nucleation after having been regulated so as to have a pH of 12.0-14.0 at a solution temperature of 25 degree centigrade, and thereafter the resultant aqueous solution, which is for particle growth and which contains formed nuclei, is regulated so as to have a pH that, at a solution temperature of 25 degree centigrade, is 10.5-12.0 and lower than in the nucleation step, thereby growing the particles. This particle growth is conducted in a non-oxidizing atmosphere having an oxygen concentration of 1 vol.% or lower, over a period which ranges from initiation of the particle growth step and which accounts for more than 40% of the whole period of the particle growth step. Furthermore, the stirring power per unit volume in at least the nucleation step is regulated to 0.5-4 kW / m3.
Owner:SUMITOMO METAL MINING CO LTD

Slowly-released filter stick essence microcapsule and preparation method thereof

The invention discloses a slowly-released filter stick essence microcapsule and a preparation method thereof. The slowly-released filter stick essence microcapsule is prepared from the following raw materials in parts by weight: 12-18 parts of sodium alginate, 6-12 parts of Arabic gum, 15-25 parts of emulsifier and 10-15 parts of filter stick essence. The preparation method comprises the following steps: firstly, respectively preparing an Arabic gum solution and a sodium alginate solution; then, injecting the sodium alginate solution into the Arabic gum solution proportionally to obtain a mixed wall material solution; in the stirring process, successively adding the emulsifier and the filter stick essence to obtain emulsion; standing; and carrying out high-voltage electrostatic treatment after foam is eliminated to obtain the microcapsule. The slowly-released filter stick essence microcapsule prepared by the invention has the advantages that the embedding rate is more than 80%, the particle diameter uniformity is good, the essence retention rate is more than 85% after the microcapsule is stored for 6 months at 20 DEG C, and the release rate of the essence microcapsule at 40 DEG C is about 6 times of the release rate of the essence microcapsule at 20 DEG C.
Owner:UNIV OF SHANGHAI FOR SCI & TECH

Method for detecting low-concentration mercury ions based on DNA modified SERS substrate

The invention discloses a method for detecting low-concentration mercury ions based on a DNA modified SERS substrate. The method comprises the following steps: preparing uniform gold-covered silicon dioxide nano particles by a fractional step method and fixing nano particles with a core-shell structure on a quartz glass sheet by a coupling agent to construct an SERS substrate; modifying single-chain DNA molecules on the surfaces of gold shell layers of the gold-covered silicon dioxide nano particles through sulfydryls; immersing the prepared DNA aptamer modified SERS substrate into a solution containing the mercury ions; washing with de-ionized water; by taking an SERS signal specific value of a G basic group and an A basic group as spectrum standard measurement of DNA at a metal surface state, realizing quantitative and specific detection on the mercury ions by analyzing a characteristic Raman peak and the change of the specific value. Compared with the prior art, the method has the following advantages that the sensitivity of the method is high, the detection lower limit is about 50nM, the measurement operation is simple, the cost is low, and the real-time and rapid measurement can be realized.
Owner:HEFEI INSTITUTES OF PHYSICAL SCIENCE - CHINESE ACAD OF SCI

Hexagonal crystal tungsten bronze short rod nanoparticles and preparation method thereof

The invention discloses a preparation method for preparing hexagonal tungsten bronze short rod nanoparticles MxWO3 with tungstate as the raw material, and belongs to the field of the nanometer technology and the field of energy conservation and environment protection. The method includes the steps of preparing high-specific-surface-area solid colloidal wolframic acid through a cation exchange method or a rapid acidification method, and synthesizing the hexagonal tungsten bronze short rod nanoparticles MxWO3 through a thermal reaction with the solid colloidal wolframic acid as the tungsten source, wherein the synthesized short rod nanoparticles are small in size and high in granularity uniformity, are in a short rod nanometer shape, have the advantages of being quite good in dispersibility and the like, and are particularly suitable for preparing a transparent thermal insulating coating and a thin film of the transparent thermal insulating coating. The visible light permeability and near infrared shielding / thermal insulating performance of the prepared powder can be further improved through nitrogen thermal treatment or reduction thermal treatment. The method is suitable for preparing the glass transparent thermal insulating coating and thermal insulating and heating compounds such as a thermal insulating thin film, a thermal insulating curtain, a solar thermal collector, a solar water heater coating, heating fiber, a thermal insulating and heat preservation plate and photothermal therapy.
Owner:DALIAN POLYTECHNIC UNIVERSITY

Nickel-manganese composite hydroxide particle and manufacturing method thereof, positive electrode active material and manufacturing method thereof and non-water-system electrolyte secondary battery

The invention provides a nickel-manganese composite hydroxide particle and a manufacturing method thereof. The nickel-manganese composite hydroxide particle has the small and uniform particle size and is of a hollow structure. According to the solution, when nickel-manganese composite hydroxide is obtained through a devitrification reaction, a nickelic metallic compound, a manganeses metallic compound and a water solution for nucleus formation of an ammonium ion donator are controlled so that the pH value of the water solution can be controlled to range from 12.0 to 13.4 with the solution temperature being 25 DEG C as the reference, nucleus formation is performed in the oxidability environment, then, a water solution for growth of the particle with the formed nucleus so that the pH value of the water solution can be controlled to range from 10.5 to 12.0 with the solution temperature being 25 DEG C as the reference, and the oxidability environment with the oxygen concentration being larger than 1% is switched into the oxygen and non-active gas mixture environment with the oxygen concentration being smaller than 1% so that the nucleus can grow.
Owner:SUMITOMO METAL MINING CO LTD

Lithium-rich manganese-based precursor, preparation method thereof and lithium-rich manganese-based positive electrode material

The invention relates to a lithium-rich manganese-based precursor, a preparation method thereof and a lithium-rich manganese-based positive electrode material. The preparation method of the lithium-rich manganese-based precursor comprises the following steps: (1) dissolving nickel salt, cobalt salt, manganese salt and doping ion salt in water to obtain a mixed salt solution; (2) adding a precipitant and a complexing agent into the mixed salt solution, and adjusting the pH value to obtain a reaction precursor; and (3) carrying out intermittent ultrasonic vibration on the reaction precursor to obtain a lithium-rich manganese-based precursor crude product. According to the invention, the pH value of the reaction system is adjusted, so that the particle size of the material is in an increasingstage; the particle size in the reaction system is controlled by adopting intermittent ultrasonic concussion; when the particle size exceeds a control index, the ultrasonic oscillator is started, sothat nucleation of the reaction system is rapidly carried out, and the particle size is reduced; and when the particle size is reduced to a qualified standard range, the ultrasonic oscillator is turned off, so that the particle size of the lithium-rich manganese-based precursor is controllable.
Owner:EVE ENERGY CO LTD

Production method of nanoscale high-purity zirconium dioxide composite powder

The invention relates to a production method of nanoscale high-purity zirconium dioxide composite powder. The method comprises the following steps: taking zirconium tetrachloride as the raw material, drying the raw material, then removing impurity with boiling point being lower than that of zirconium tetrachloride and impurity with boiling point being higher than that of zirconium tetrachloride through a two-step distillation crystallization method, dissolving zirconium tetrachloride by using a mixed solution of deionized water and alcohol, carrying out separation of zirconium and hafnium in the solution through an MIBK extraction-elution resin filled extraction chromatographic column, then further purifying zirconium tetrachloride through an ion exchange mode, adding chloride into a high-purity zirconium tetrachloride solution to form a zirconium tetrachloride compound solution, then obtaining zirconium hydroxide gel through an ammonia water spraying co-precipitation manner, carrying out hydrothermal reaction of the zirconium hydroxide gel in a high-pressure reactor, and finally filtering, washing and drying to obtain the nanoscale high-purity zirconium dioxide composite powder. The nanoscale high-purity zirconium dioxide composite powder prepared by the method has the advantages of high purity, uniform particle size, high dispersibility and the like and is applicable to industrial production.
Owner:南京金鲤新材料有限公司

Nickel composite hydroxide and manufacturing method thereof, cathode active material for nonaqueous-electrolyte secondary battery and manufacturing method thereof, and nonaqueous-electrolyte secondary battery

Provided are a cathode active material having a suitable particle size and high uniformity, and a nickel composite hydroxide as a precursor of the cathode active material. When obtaining nickel composite hydroxide by a crystallization reaction, nucleation is performed by controlling a nucleation aqueous solution that includes a metal compound, which includes nickel, and an ammonium ion donor so that the pH value at a standard solution temperature of 25 DEG C. becomes 12.0 to 14.0, after which, particles are grown by controlling a particle growth aqueous solution that includes the formed nuclei so that the pH value at a standard solution temperature of 25 DEG C. becomes 10.5 to 12.0, and so that the pH value is lower than the pH value during nucleation. The crystallization reaction is performed in a non-oxidizing atmosphere at least in a range after the processing time exceeds at least 40% of the total time of the particle growth process from the start of the particle growth process where the oxygen concentration is 1 volume % or less, and with controlling an agitation power requirement per unit volume into a range of 0.5 kW / m3 to 4 kW / m3 at least during the nucleation process.
Owner:SUMITOMO METAL MINING CO LTD

Microcapsule with silicon dioxide core-shell coating liquid and preparation method of microcapsule

ActiveCN103551093ASolve the problem that it cannot be coated into microcapsulesImprove thermal stabilityMicroballoon preparationMicrocapsule preparationMicrosphereHeat stability
The invention discloses a microcapsule with a silicon dioxide core-shell coating liquid and a preparation method of the microcapsule. The preparation method comprises the following steps of: selecting a polymer monomer A to prepare a polymer microsphere B with uniform grain size and having positive charge on the surface; absorbing a surface active agent onto the surface of the microsphere B to obtain a seed microsphere C; coating the seed microsphere C with tetraethoxysilane to obtain a microsphere D with porous silicon dioxide as a shell; calcining the microsphere D to obtain a hollow silicon dioxide microsphere E; soaking the hollow silicon dioxide microsphere E into liquid of a core material to obtain a microsphere F with the core material; coating the microsphere F with tetraethoxysilane to obtain the core-shell structured microcapsule G with dense silicon dioxide as the shell. The method is applicable to the preparation of the microcapsule coating low-polarity liquid, high-polarity liquid and dual-polarity liquid, solves the problem in the prior art that the dual-polarity liquid cannot be coated into the microcapsule, is simple in operation steps, and low in requirement for equipment, and the microcapsule is high in heat stability, good in corrosion resistance and uniformity of grain size.
Owner:INST OF CHEM MATERIAL CHINA ACADEMY OF ENG PHYSICS +1

Preparation method of propofol fat emulsion injection

The invention discloses a preparation method of a propofol fat emulsion injection. The preparation method comprises the following steps: uniformly mixing soybean oil, lecithin and oleic acid and adding propofol; spraying an oil phase into a water phase under the protection of nitrogen gas to prepare emulsion; shearing the emulsion to obtain primary emulsion; homogenizing the primary emulsion under the pressure of 10000psi-20000psi to prepare an emulsion semi-finished product; and filtering, inflating nitrogen and sterilizing to prepare the propofol fat emulsion injection. According to the preparation method, the grain diameter uniformity is enhanced and the disadvantage that the grain diameter deviation of the primary emulsion is too great is improved; the stability of finished-product emulsion is improved; the average grain diameter of the detected emulsion is 210nm-230nm and the grain diameter deviation is 0.20-0.30; the requirements on the grain diameters by the fat emulsion injection are met; the emulsion grains with the size being more than 1 micron are not detected, and the grain diameters are obviously better than the standards that the content of the emulsion grains with the size being 1 micron in emulsion large grains of national drug standards is not more than 3%; the physicochemical properties are stable, the toxic side effect is low, the pains caused by injection are reduced, and the compliance of using drugs by patients is increased, so that the application prospect is very good.
Owner:HEBEI YIPIN PHARMA

Full-fat extruded soybean production device and production technology

The invention discloses a full-fat extruded soybean production device and a production technology. The full-fat extruded soybean production device comprises a bulk bin, an impurity removal working section, a first crusher and a second tee, wherein a material outlet of the second tee is connected with a peel suction device for removing soybean peels, and another material outlet of the second tee is connected with the first crusher; an arch breaking feeding bin is connected with a tempering device; the material outlet end of the tempering device is connected with an extruding machine; the material outlet end of the extruding machine is connected with a cooler; the material outlet end of the cooler is connected with a second crusher; another material outlet of a third tee is connected with the first crusher; the material outlet end of the second crusher is connected with a first rotary vibration grading sieve; the first rotary vibration grading sieve is connected with a first packaging device. The full-fat extruded soybean production device has the advantages that soybeans are firstly broken and then crushed, so that the productivity of the first crusher is increased, the abrasion of a hammer blade is reduced, and the crushing effect is improved; the peel suction device is used for separating soybean peels from soybean halves, so that the quality of a finished extruded soybean product is mainly improved.
Owner:江苏丰尚油脂工程技术有限公司
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