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30results about How to "No complicated steps" patented technology

Method for rapidly measuring p-hydroxy-benzoate ester in cosmetics

The invention discloses a method for rapidly measuring a p-hydroxy-benzoate ester in cosmetics and relates to a method for measuring components in the cosmetics. The method comprises the following steps: A, treating a sample to be measured; B, establishing a background spectral database, namely B1, acquiring spectral data of a cosmetic sample; B2, acquiring spectral data of components to be measured; B3, converting the data format; B4, acquiring spectral data of a background which does not contain the components to be measured; B5, reducing the dimensionality of a background database; C, acquiring a standard spectral database v of the p-hydroxy-benzoate ester; D, measuring a spectrum of the cosmetic sample to be measured; E, measuring the content of the p-hydroxy-benzoate ester in the cosmetic sample to be measured. The method is high in analysis efficiency, low in operating strength and low in analysis cost, the background database which does not contain the measured components is not required to be accumulated, the machine hour and the reagent loss can be reduced, the robustness is high, and the method is simple and suitable for rapidly analyzing and measuring the same type of large-scale samples.
Owner:GUANGXI UNIVERSITY OF TECHNOLOGY

Method for measuring p-hydroxybenzoate in cosmetics

The invention discloses a method for measuring p-hydroxybenzoate in cosmetics and relates to a method for measuring components in cosmetics. The method comprises the following steps: A, performing tested sample treatment, namely preparing the tested cosmetics into diluent; B, performing spectral measurement, namely B1, preparing a background spectrum set, B2, determining the standard spectrum of p-hydroxybenzoate, and B3, performing spectral measurement on the tested cosmetics; C, performing positive test and content measurement, namely C1, performing positive test, calculating an included angle between the merged matrix and the standard spectrum of p-hydroxybenzoate, when the included angle is larger than 0.15, the p-hydroxybenzoate is judged to be negative, and the spectrum of the tested cosmetics is recorded into the background spectrum database, and when the included angle is smaller than 0.1, the p-hydroxybenzoate is stored in the tested cosmetics, the sample is positive, and continuing, and C2 performing content measurement, namely deducing the standard spectrum of p-hydroxybenzoate from the spectrum of the tested cosmetics, thereby obtaining the actual content of the p-hydroxybenzoate. The method is high in analysis efficiency, low in operation strength, low in analysis cost, high in robustness and easy to popularize and use.
Owner:GUANGXI UNIVERSITY OF TECHNOLOGY

Method for treating methylene blue dye wastewater

The invention relates to a method for treating methylene blue dye wastewater. Firstly, diatomite is evenly mixed with calcium raw materials, alkali activator and water, and is put in a high-pressure hydrothermal reaction kettle after the compression molding to react for 1-48 hours at the temperature of 100-200 DEG C to obtain a diatomite-based porous adsorbent containing C-S-H, tobermorite and analcite; then, the diatomite-based porous adsorbent is put in a conical bottle accommodated with a liquid culture medium; 5-20% of yeast powder by mass is added to regulate the pH to be 5-8 and to cultivate for 2-48 h under the constant-temperature condition of 15-35 DEG C on a reciprocal shaking table with the speed of 60-120 rpm so as to obtain a yeast-loaded diatomite-based porous adsorbent; finally, 1-10 g of the yeast-loaded porous adsorbent is added in the methylene blue dye wastewater with per liter concentration of 100-1000 mg / L to treat for 1-48 h at the temperature of 25-45 DEG C on the reciprocal shaking table with the pH of 4 to 10 and the speed of 60-120 rpm; the concentration of the treated methylene blue wastewater is measured through a spectrophotometer method; the result shows that the removal rate of the methylene blue dye exceeds 90%. The method has the advantages of simple process, low cost and no secondary pollution, and is suitable for the industrial treatment of the methylene blue dye wastewater.
Owner:TONGJI UNIV

High-purity battery-level manganese source and preparation method thereof

The invention provides a high-purity battery-level manganese source which is manganese sulfide and / or manganese oxide, wherein a manganese sulfide XRD crystal phase is a pure gamma-phase and / or pure beta-phase similar-fibrid or claviform sulfide, and the appearance is pink, brownish red or brick red. The preparation method of the high-purity battery-level manganese source comprises the following steps of preparing a divalent manganese salt solution to the concentration of 5-50 degrees Be'; adding sulphurizing salt, and filtering to prepare a primary manganese salt solution; further adding a sulfide solution, and regulating pH to prepare a manganese sulfide filter cake; carrying out reverse osmosis washing to obtain a manganese sulfide crystal; beating, then controlling the temperature of manganese sulfide slurry to 50-100 DEG C, stirring, adding an acid source to the manganese sulfide slurry to react for 2-6 hours, carrying out acidolysis to prepare a manganese salt solution, wherein the manganese sulfide inside a system needs to be excessive during the acidolysis, and the excessive mass fraction of the manganese sulfide is controlled at 1%-10%; regulating the pH to 5.5-6.0, reacting for 2-6 hours, and then carrying out pressure filtration to obtain a high-purity battery-level manganese salt product. The manganese sulfide can not only be directly applied, but also be used for synthesizing different kinds of high-end manganese salt or manganese oxide by taking the obtained manganese sulfide as the high-purity manganese source.
Owner:深圳市北宸创新材料科技有限公司

Method for measuring junction temperature and thermal resistance of metal-oxide semiconductor tube

The invention discloses a method for measuring the junction temperature and thermal resistance of a metal-oxide semiconductor tube. The method comprises the following steps of: placing an insulating substrate with a device to be measured into a temperature control box, and adjusting the temperature control box to 25 DEGC; applying a DC (direct current) voltage to the drain end and source end of the device to be measured, and applying a grid DC working voltage to the grid; measuring the current at the drain and source ends of the device to be measured when the voltage on the grid is a DC working voltage; removing the DC working voltage on the grid; applying a square-wave pulse voltage to the grid; gradually increasing the temperature in the temperature control box, wherein the maximum temperature does not exceed the junction temperature of the measured device; continuously measuring the leakage current at the drain and source ends of the device to be measured; and when the measured leakage current at the drain and source ends of the device to be measured is equal to the current at the drain and source ends of the device to be measured, calculating the thermal resistance of the device to be measured by taking the temperature in the temperature control box as an equivalent junction temperature.
Owner:SOUTHEAST UNIV

A method for preparing high-basic chromium-vanadium-titanium pellets by using calcium oxide

ActiveCN109852791BGood for bonding into ballsHigh compressive strengthSodium BentoniteDry mixing
The invention relates to a method for preparing high-alkalinity chromium-containing vanadium-titanium pellets by adopting calcium oxide. The method comprises the following steps of mixing the raw materials including vanadium titano-magnetite, additive calcium oxide powder and sodium bentonite, so that the alkalinity of the raw materials is 1.8 to 2.1, drying and drying respectively, and carrying out dry mixing and mixing; averagely distributing the mixed ore materials into two parts, adding water accounting for 3% to 4% of the total mass of the raw materials in the first part, adding water with the total mass of 6% to 8% of the total mass of the raw materials in the second part, uniformly mixing, and hermetically standing; when pelletizing is carried out, a first part of mineral powder isused in the forming period of the master ball, a second part of mineral powder is used in the growth period of the master ball, the water spraying amount before the growth of the master ball is controlled to be 1ml of 10g of ore powder to 2ml of 10g of ore powder of mineral powder, preventing adhesion between the master balls, and adding water for 40 seconds to 90 seconds at each time, so that thediameter of the prepared pellets ranges from 8mm to 12mm; and preparing raw ball braised material, drying, pre-xidizing and roasting, carrying out secondary high-temperature oxidation roasting to obtain high-alkalinity chromium-containing vanadium-titanium pellets.
Owner:NORTHEASTERN UNIV LIAONING

Method for measuring p-hydroxybenzoate in cosmetics

The invention discloses a method for measuring p-hydroxybenzoate in cosmetics and relates to a method for measuring components in cosmetics. The method comprises the following steps: A, performing tested sample treatment, namely preparing the tested cosmetics into diluent; B, performing spectral measurement, namely B1, preparing a background spectrum set, B2, determining the standard spectrum of p-hydroxybenzoate, and B3, performing spectral measurement on the tested cosmetics; C, performing positive test and content measurement, namely C1, performing positive test, calculating an included angle between the merged matrix and the standard spectrum of p-hydroxybenzoate, when the included angle is larger than 0.15, the p-hydroxybenzoate is judged to be negative, and the spectrum of the tested cosmetics is recorded into the background spectrum database, and when the included angle is smaller than 0.1, the p-hydroxybenzoate is stored in the tested cosmetics, the sample is positive, and continuing, and C2 performing content measurement, namely deducing the standard spectrum of p-hydroxybenzoate from the spectrum of the tested cosmetics, thereby obtaining the actual content of the p-hydroxybenzoate. The method is high in analysis efficiency, low in operation strength, low in analysis cost, high in robustness and easy to popularize and use.
Owner:GUANGXI UNIVERSITY OF TECHNOLOGY

Seamless steel tube for nuclear power equipment and preparation method of seamless steel tube

InactiveCN108486479AGood yield strengthGood wear resistanceSteel tubeNuclear power plant
The invention relates to a seamless steel tube for nuclear power equipment and a preparation method of the seamless steel tube. The seamless steel tube comprises the following compositions of, by mass, 1.5-3.3 parts of C, 1.9-4.2 parts of Si, 4.5-8.5 parts of Mn, 0.1-0.2 part of Pb, 0.1-0.2 part of Bi, 0.2-0.4 part of Nb, 6-12 parts of Re, 0.06-0.15 part of P and 950-1100 parts of Fe. According tothe provided seamless steel tube, the technical requirements for the seamless steel tube for a third generation nuclear power plant unit can be met, the performance of the seamless steel tube is higher than the performance of a conventional seamless steel tube, the excellent yield strength, tensile performance, toughness performance and impact performance are achieved at the low temperature, hightemperature and normal temperature, the quite good abrasion resistance is achieved, and the service life of the steel tube is long.
Owner:ZHANGJIAGANG FREE TRADE ZONE HENGLONG STEEL TUBE

Prostatic puncture device

The invention discloses a prostatic puncture device, and relates to the field of medical equipment. According to the technical scheme, the prostatic puncture device comprises a base, wherein the baseis provided with a sliding groove, the upper side of the base is slidably connected with a prostatic supporting mechanism and a puncture needle through the sliding groove in sequence, the prostatic supporting mechanism is located at the front side of the point of the puncture needle, and the prostatic supporting mechanism and the puncture needle are slidably connected with the sliding groove through supporting rods respectively; the prostatic supporting mechanism comprises an outer cylinder, the outer cylinder is a hollow cylinder of which the two ends are provided with openings, and the outercylinder is internally in sleeved connection with an internal assembly; the rear side end of a supporting assembly is hinged with the front side end of an inner rod. The prostatic puncture device hasthe advantages that the use is simple, no complex operation step exists, the smoother outer cylinder of the device enters the anus of a patient more easily, and the supporting assembly of the devicecan be unfolded after the device enters the human body, thereby reducing the pain of the patient, and ensuring the enough supporting area and supporting strength for the prostate.
Owner:QINGDAO TUMOR HOSPITAL

A kind of high-purity battery grade manganese source and preparation method thereof

The invention provides a high-purity battery-level manganese source which is manganese sulfide and / or manganese oxide, wherein a manganese sulfide XRD crystal phase is a pure gamma-phase and / or pure beta-phase similar-fibrid or claviform sulfide, and the appearance is pink, brownish red or brick red. The preparation method of the high-purity battery-level manganese source comprises the following steps of preparing a divalent manganese salt solution to the concentration of 5-50 degrees Be'; adding sulphurizing salt, and filtering to prepare a primary manganese salt solution; further adding a sulfide solution, and regulating pH to prepare a manganese sulfide filter cake; carrying out reverse osmosis washing to obtain a manganese sulfide crystal; beating, then controlling the temperature of manganese sulfide slurry to 50-100 DEG C, stirring, adding an acid source to the manganese sulfide slurry to react for 2-6 hours, carrying out acidolysis to prepare a manganese salt solution, wherein the manganese sulfide inside a system needs to be excessive during the acidolysis, and the excessive mass fraction of the manganese sulfide is controlled at 1%-10%; regulating the pH to 5.5-6.0, reacting for 2-6 hours, and then carrying out pressure filtration to obtain a high-purity battery-level manganese salt product. The manganese sulfide can not only be directly applied, but also be used for synthesizing different kinds of high-end manganese salt or manganese oxide by taking the obtained manganese sulfide as the high-purity manganese source.
Owner:深圳市北宸创新材料科技有限公司
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