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235results about How to "Ease of mass industrial production" patented technology

Porous polymer nanoparticles and preparation method thereof

The invention provides porous polymer nanoparticles and a preparation method thereof. The porous polymer nanoparticles are prepared by an emulsion polymerization method, and have the adjustable porous size, the monodisperse particle size, the adjustable particles size and a high specific area. Compared with the traditional porous polymer particles, the porous polymer nanoparticles have the porous size with adjustable range of between 0.5 and 100nm, the monodisperse particle size, and the particles size with adjustable range of between 20 and 200nm, so the porous polymer nanoparticles can be used as a catalyst carrier, a separation membrane, a gas storage material, a medicament carrier of animal and plant cells, a medicament carrier of animal and plant tissues and a novel template agent of a complex structure material. The preparation method comprises the following steps of: polymerizing a styrene monomer and a divinylbenzene monomer by the emulsion polymerization method to obtain a precursor of the monodisperse porous polymer nanoparticles; and then performing ultra-crosslinking on the precursor of the monodisperse porous polymer nanoparticles by an internal crosslinking method or an external crosslinking method to obtain the monodisperse porous polymer nanoparticles.
Owner:武汉华科中英纳米科技有限公司

Method and system for recovering main associated elements from copper-nickel sulfide ore

The invention provides a method and system for recovering main associated elements from copper-nickel sulfide ore. The method comprises the following steps: 1, continuously adding low-grade nickel matte and a leaching reaction solution into a reaction base solution, carrying out selective leaching, and collecting hydrogen sulfide gas, a first leaching solution and a first leaching residue, wherein the leaching reaction liquid is sulfuric acid with the mass fraction being 60-95%; 2, adding water into the first leaching residue for dissolving the first leaching slag, and collecting a second leaching solution and a second leaching residue; and 3, removing iron from the second leaching solution, collecting an iron-removed solution used for extracting nickel and cobalt and an iron-removed residue used for iron making, and / or sending the second leaching residue to a copper smelting device for smelting to obtain copper and noble metal. According to the method, deep separation of the nickel and the copper can be realized, and recovery of the nickel, the copper, the cobalt, the noble metal and sulfur can be effectively realized. The method is simple in process, short in flow and high in efficiency, is a clean and efficient element recovery process and is easy for large-scale industrial production.
Owner:CENT SOUTH UNIV

Method for manufacturing monolithic bipolar membrane

The invention relates to a method for manufacturing a monolithic bipolar membrane, which comprises the following steps of: immersing a substrate membrane in a solution containing styrene, divinybenzene and benzoyl peroxide, pressurizing the immersed membrane, wherein the substrate membrane is a thin alloy membrane formed by two-element blending of polyethylene and ethylene-octylene copolymer elastomer or by three-element blending of polyethylene, ethylene-octylene copolymer elastomer and polyisobutylene rubber; and pressurizing the membrane immersed in the solution and polymerizing under the condition of heating to obtain a base membrane; sulfonating one side face of the base membrane by heating in concentrated sulfuric acid; performing chloromethylation reaction of the membrane with one sulfonated side face in chloromethyl ether containing anhydrous stannic chloride so that the other side face of the membrane is chloromethyl; and immersing the membrane in a trimethylamine aqueous solution or a trimethylamine aqueous solution containing dimethylamine to carry out an aimination or quaterisation reaction to obtain the monolithic bipolar membrane. The method has the advantages that the immersing temperature is greatly reduced, the styrene and divinybenzene solution can be repeatedly used, and the electric resistance of the bipolar membrane is low. The bipolar membrane has a catalytic layer for accelerating water decomposition, the method is simple and convenient and is easy for large-scale industrialized production.
Owner:福建省延润膜环保科技有限公司

Voriconazole phosphate ester for injection and preparation method thereof

The invention provides voriconazole phosphate ester for injection and a medicinal salt thereof and a preparation method for the voriconazole phosphate ester for injection and the medicinal salt thereof. The preparation method comprises the following steps: adding 5 to 98 percent water for injection in a liquid preparation container; adding 90 to 110 percent of the accurate formula dosage of voriconazole phosphate ester and the medicinal salt thereof in the container; stirring the mixture; slowly dropwise adding a pH value regulator; regulating pH to between 6.0 and 11; supplementing water to the full dosage and then adding 0.01 to 1.0 percent (weight in volume) medicinal carbon into the product; stirring the mixture for 15 to 60 minutes; using a sand filter stick to carry out rough filtration and decarburization on the obtained product, and using a 0.22mum millipore filter to carry out fine filtration on the product until the clarity is qualified; after determining that the content of the midbody is qualified, determining the filling quantity and subpackaging the finished product in the vial; adding the semi-plug; carrying out freezing and drying on the sample; controlling the moisture content between 1 and 8 percent; pressing the plug; and carrying out capping.
Owner:HC SYNTHETIC PHARMA CO LTD

A method of manufacturing a monolithic bipolar membrane

The invention relates to a production method of a single-sheet bipolar membrane, and belongs to the technical field of preparation of a membrane separation material in the field of chemical engineering. The production method comprises the following steps: a polyolefin membrane or a polyhaloalkene membrane is taken as a substrate membrane; the substrate membrane is immersed into a monomer solution filled with styrene-divinylbenzene, nitrogen is fed, the mixture is sealed and then placed in a radiation source chamber for radiation, and then the mixture is taken out to obtain the base membrane; one side surface of the base membrane is heated for sulfonation in concentrated sulfuric acid or chlorosulfonic acid, and a positive surface membrane of the bipolar membrane is formed; the membrane with one sulfonated side surface has a chloromethylation reaction in chlorosulfonic acid containing tin tetrachloride anhydrous to obtain the membrane with a chloromethyl group on the other side surface, the membrane is then immersed in a trimethylamine aqueous solution or a dimethylamine-containing trimethylamine aqueous solution for an amination or quaterization reaction to form a negative surface membrane of the bipolar membrane, and the single-sheet bipolar membrane is formed. The prepared bipolar membrane has low resistance and low transmembrane voltage, and the production method is simple and convenient and facilitates large-scale industrial production.
Owner:福建省延润膜环保科技有限公司

Rare earth-magnesium-transition metal base hydrogen storage metal and preparation method thereof

The invention relates to a rare earth-magnesium-transition metal base hydrogen storage metal with high hydrogen storage capacity and moderate hydrogen storage temperature and preparation method thereof. The metal is characterized in that the chemical formula thereof is REMgxMy, wherein x is more than 1 and less than 2, y is more than 1 and less than 3; RE is one or more than one of rare earth metals of La, Ce, Pr, Nd, cerium rich mish metal Mm and lanthanum rich mish metal M1; M is one or more than one of transition metals of Cu, Ni, Mn, Fe and Zn. The rare earth-magnesium-transition metal base hydrogen storage metal provided by the invention is also characterized in that the metal at least contains a multiphase structure of CeMg3 type LaMg3 phase and LaMg2Cu2 phase. The invention also provides a preparation method of the rare earth-magnesium-transition metal base hydrogen storage metal. The preparation method mainly includes that induction melting is adopted, Mg base master alloy is utilized to substitute magnesium and used as raw material, secondary charging is used for preparing the metal, and the metal is annealed. The hydrogen storage metal of the invention has the advantages that the hydrogen storage capacity at 200 DEG C is more than 3wt% and the metal can be used as solid-state hydrogen storage material.
Owner:YANSHAN UNIV

Freeze-drying composition of posaconazole prodrug and preparation method and application of freeze-drying composition of posaconazole prodrug

The invention relates to a freeze-drying composition of a posaconazole prodrug and a preparation method and application of the freeze-drying composition of the posaconazole prodrug. The freeze-drying composition has the advantages that the freeze-drying composition is high in water solubility, and safety of the freeze-drying composition is guaranteed due to the fact that cyclodextrins auxiliary materials need not to be added during the preparation of the freeze-drying composition; the freeze-drying composition is suitable for being used for treating various amphotericin-intolerant or refractory adult invasive fungal infections; the freeze-drying composition is used as a preventive drug for high-risk patients, the freeze-drying composition is applicable to patients above 13 years old and with impaired immunity and especially applicable to patients who have graft versus host disease (GVHD) after hematopoietic stem cell transplant, patients with leukemia and patients with long-term leukopenia due to chemotherapy; compared with control drugs such as fluconazole and itraconazole, the freeze-drying composition can effectively prevent invasive aspergillosis and can lower the mortality related to the invasive fungal infections.
Owner:HC SYNTHETIC PHARMA CO LTD

Preparation method of forward osmosis membrane modified with oxidized graphene

The invention provides a preparation method of a forward osmosis membrane modified with oxidized graphene. The preparation method comprises the following steps: 1, firstly, conducting ultrasonic dispersion on the oxidized graphene in high-polarity organic solvent, so that homogeneous dispersion liquid is obtained; 2, adding organic solvent of raw materials of a produced membrane to the dispersion liquid; 3, sequentially adding additives and the produced membrane to the dispersion liquid obtained in step 2, and stirring the mixture till the mixture is dissolved completely, so that casting membrane liquid is obtained; 4, conducting sufficient defoaming on the casting membrane liquid in a vacuum drying box, then pouring the casting membrane liquid on a glass plate where a support layer is laid, and conducting membrane scraping; 5, after membrane pouring is ended and the casting membrane liquid is volatilized in air, putting the casting membrane liquid in a coagulation bath; 6, separating a membrane piece with the glass plate, and putting the membrane piece into pure water for immersion; 7, conducting natural drying on the membrane which is sufficiently immersed as mentioned above, so that the forward osmosis membrane is obtained. The modified forward osmosis membrane prepared through the preparation method is good in hydrophilicity and water flux and great in antipollution capability, cleaning expense of the membrane is lowered, the service life of the membrane is greatly prolonged, and mechanical properties are improved a lot.
Owner:HARBIN ENG UNIV

600 MPa-grade highly-chambered steel plate for automotive chassis and manufacturing method thereof

The invention provides a 600 MPa-grade highly-chambered steel plate for automotive chassis. Steel of the steel plate is composed of, in percentage by weight, 0.04-0.10% of C, Si smaller than 0.70%, 1.0-1.6% of Mn, 0.02-0.08% of Als, 0.01-0.05% of Nb, P smaller than 0.015%, S smaller than 0.005% and the balance Fe and inevitable impurities. The invention further provides a manufacturing method of the steel plate. The method comprises the steps of heating continuous casting sheet billets with the thickness ranging from 80 mm to 230 mm to 1220+ / -20 DEG C, and preserving the temperature for 1.8-3 hours; carrying out two-stage rolling, wherein the rolling temperature of the recrystallizing region is higher than 1050 DEG C, the thickness of intermediate billets ranges from 35 mm to 60 mm, the finish rolling temperature of the non-recrystallizing region ranges from 840 DEG C to 920 DEG C, and the thickness of finished products ranges from 2.0 mm to 6.0 mm; carrying out continuous laminar flow cooling after finish rolling, wherein the cooling rate is 20-40 DEG C / s and the coiling temperature ranges from 450 DEG C to 580 DEG C. According to the invention, the steel plate is high in alloy content and low in cost, the hot rolling process is simple, the rolling performance of the steel plate is uniform, and the matching performance between the strength and the hole chambering rate is good.
Owner:ANGANG STEEL CO LTD

Thin-film solar cell and method for preparing same

The invention provides a thin-film solar cell. Electrode grooves are formed in a low-resistance window layer, and collection electrodes are deposited in the electrode grooves respectively. On the premise that the thickness of a buffer layer and the thickness of a high-resistance window layer are large enough so that the density of a film layer of the thin-film solar cell can be ensured, the photon-generated carrier recombination probability of an interface can be effectively lowered. Due to the fact that the collection electrodes are arranged in the electrode grooves respectively, the thickness of the portions, in the perpendicular direction of the contacting areas of the collection electrodes and the electrode grooves, of the high-resistance window layer can be reduced, the internal resistance of the solar cell can be effectively reduced, the output power of the solar cell can be improved, meanwhile, the contact area between the collection electrodes and a transparent window layer composed of the high-resistance window layer and the low-resistance window layer is increased, the collection rate of the collection electrodes for photon-generated carriers is improved, and the output power of the thin-film solar cell is further improved. In addition, a method for preparing the thin-film solar cell is simple in process and allows large-scale industrial production to be easily achieved.
Owner:DONGTAI HI TECH EQUIP TECH (BEIJING) CO LTD

Method for recycling active materials and aluminum foil from waste lithium-ion battery cathode materials

The invention discloses a method for recycling active materials and aluminum foil from waste lithium-ion battery cathode materials, and belongs to the technical field of electrode material recycling. The method comprises the steps that waste lithium-ion batteries are discharged, disassembled and then cut, and cathode sheets are obtained; the cathode sheets are put into a sulfuric acid solution to be soaked for 2 min to 10 min to enable cathode active materials to be separated from aluminum foil, wherein the concentration of the sulfuric acid solution ranges from 1.0 mol/L to 3.0 mol/L, and the temperature of the sulfuric acid solution ranges from 40 DEG C to 60 DEG C; and the aluminum foil is taken out, washed and dried, the dried aluminum foil is obtained, the solution containing the cathode active materials is filtered, filter residues are washed and dried, the cathode active materials are obtained, the cathode active materials are subjected to a wet leaching process, valuable metals in the cathode active materials are recycled, and filtrate is recycled or serves as a slurrying liquid of the wet leaching process. According to the method for recycling the active materials and aluminum foil from the waste lithium-ion battery cathode materials, the problem that the cathode active materials and the aluminum foil cannot be effectively and thoroughly separated in the waste lithium-ion battery recycling process is solved, the technology is simple, the flow is short, the recycling cost is low, large-scale industrial production is easy to achieve, secondary pollution is not generated in the recycling process, and the method is friendly to the environment.
Owner:JINCHUAN GROUP LIMITED

Method for recycling positive electrode material of waste lithium iron phosphate battery

The invention relates to a method for recycling a positive electrode material of a waste lithium iron phosphate battery. The method comprises the following steps of: (1) adding water into positive electrode powder of the waste lithium iron phosphate battery to prepare slurry, preheating the slurry, adding 98% sulfuric acid for leaching, and performing solid-liquid separation after the leaching is completed to respectively obtain leachate and leaching residues; (2) adjusting the pH value of the leachate, adding iron powder to replace and remove copper, continuously adjusting the pH value, removing aluminum by precipitation, and carrying out solid-liquid separation to obtain an impurity-removed solution; (3) supplementing sodium phosphate to adjust the mass ratio of iron to phosphorus; (4) introducing hydrogen peroxide below the liquid level of the base solution, spraying alkali liquor and the impurity-removed solution by using spraying equipment, adjusting the pH value, aging for 5-7 hours after iron in the solution is completely oxidized and precipitated, and performing solid-liquid separation to respectively obtain an iron phosphate precipitate and a lithium-containing solution; and (5) adjusting the pH value of the lithium-containing solution, and carrying out evaporation concentration and solid-liquid separation to obtain filtrate; and introducing carbon dioxide into the filtrate to obtain precipitated lithium. The method is simple, efficient and easy for batch industrial production.
Owner:JINCHUAN GROUP LIMITED +1

Cobalt-ion-doped iron-nickel magnetic microsphere and application thereof

The invention relates to a cobalt-ion-doped iron-nickel magnetic microsphere and application thereof and belongs to the technical field of chemical materials. The cobalt-ion-doped iron-nickel magnetic microsphere is mainly characterized in that cobalt ions and nickel ions are mixed and used in a magnetic sphere preparation process, the cobalt ions accounts for 20 to 30% of the total mole number of the cobalt ions and the nickel ions, and optimally, the cobalt ions accounts for 25% of the total mole number of the cobalt ions and the nickel ions. The synthesized cobalt-ion-doped iron-nickel magnetic microsphere disclosed by the invention can be directly applied to purifying target protein with a histidine tag, and other modification like antibody modification on the surface of the magnetic sphere is avoided; furthermore, the cobalt-ion-doped iron-nickel magnetic microsphere has good dispersion and quick and high-efficiency application effect and is superior to a no-cobalt-doped iron-nickel magnetic microsphere; separation performance of the cobalt-ion-doped iron-nickel magnetic microsphere is similar to that of imported coordinate-bond nickel-ion sepharose gel; the cobalt-ion-doped iron-nickel magnetic microsphere further can achieve magnetic separation and can replace imported separation materials.
Owner:DALIAN NATIONALITIES UNIVERSITY

Low-cost high-strength high-plasticity zirconium-based amorphous composite and preparation method thereof

InactiveCN110592500AHave the ability to formReduce manufacturing costElectric arc furnaceAlloy composite
The invention discloses a low-cost high-strength high-plasticity zirconium-based amorphous composite. The formula of the low-cost high-strength high-plasticity zirconium-based amorphous composite is Zr58.5Ti14.3Nb5.2Cu6.1Ni4.9Be11.0. A preparation method comprises the following specific steps of A, preparing materials, wherein Zr, Ti, Nb, Cu, Ni and Be metal raw materials are weighed and fetched according to the composition and atomic percent of Zr58.5Ti14.3Nb5.2Cu6.1Ni4.9Be11.0; B smelting master alloy, wherein a vacuum arc furnace water cooling copper crucible smelting method is adopted, theabove metal raw materials are smelted into uniform master alloy ingots; C forming the composite, wherein a vacuum die casting metal die formation rapid cooling method is adopted, the master alloy ingots are made into a casting of the zirconium-based amorphous alloy composite. The low-cost high-strength high-plasticity zirconium-based amorphous composite solves the problems that an existing zirconium-based amorphous alloy is poor in indoor temperature plasticity and high in raw material cost; the prepared zirconium-based amorphous alloy composite is low in cost and high in strength and indoortemperature plasticity and can be applied to industrial production.
Owner:东莞宜安新材料研究院有限公司
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