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34results about How to "Uniform microscopic morphology" patented technology

Bimetal-doped VIB-group metal oxide nano-material, preparation method therefor and application of bimetal-doped VIB-group metal oxide nano-material

The invention discloses a bimetal-doped VIB-group metal oxide nano-material, a preparation method therefor and an application of the bimetal-doped VIB-group metal oxide nano-material. A chemical formula of the VIB-group metal oxide nano-material disclosed by the invention is AxByMO3, wherein M is a VIB group element, A and B are dope elements present in the form of metal cations, O is an oxygen element, x is not smaller than 0 and not greater than 1, y is not smaller than 0 and not greater than 1, and the A and the B are one of different and self-existent main-group or subgroup elements. The metal oxide nano-material is prepared from a VIB-group metal element containing compound, a reducer and A-and-B-containing substances under hydrothermal conditions. The prepared bimetal-doped VIB-group oxide nanoparticles have very high near-infrared screening capacity and can be applied to the fields of photo-control materials and devices, glass energy saving and the like.
Owner:BEIJING UNIV OF CHEM TECH

Permeable type asphalt regenerant and preparation method thereof

The invention relates to a permeable type asphalt regenerant and a preparation method thereof, belonging to the technical field of resource environmental chemistry. By virtue of a surfactant, aged asphalt can be rapidly moisturized through the regenerant, the blending of basic components in the aged asphalt can be realized through higher content of aromatics in the regenerant, oil in waste oil hasbetter permeability and lubrication to the aged asphalt, thus being beneficial to interaction of macromolecules and further increasing the plasticity of the asphalt; the polar groups in epoxidized soybean oil and dibutyl phthalate have chemical reaction with asphaltene to weaken the strong attraction between asphaltene molecules, so that the agglomerated asphaltene in the aged asphalt is evenly dissolved and dispersed in the asphalt colloid system again, and a spatial network structure formed due to agglomeration of asphaltene is destructed to weaken the barrier of the spatial network structure on the permeation of the regenerant, so that the permeation capability of the regenerant is improved, and the colloid structure and performances of the aged asphalt can be effectively restored.
Owner:周荣

Two-dimensional nitrogen-doped porous carbon nanosheet and preparation method thereof

The invention relates to the field of new-type flexible electrode materials and in particular to a two-dimensional nitrogen-doped porous carbon nanosheet and a preparation method thereof. The preparation method comprises the following steps: (1) preparing a carbon nanosheet: performing first calcining on a carbon material in protection of an inert gas, cooling, and preparing the carbon nanosheet;(2) preparing a porous carbon nanosheet: adding the carbon nanosheet to oxidized acidic solution and performing an oxidation reaction, preparing the porous carbon nanosheet; and (3) preparing the two-dimensional nitrogen-doped porous carbon nanosheet: adding the porous carbon nanosheet and a surfactant to water, uniformly dispersing, adding a nitrogen-doped material, dissolving, uniformly mixing,after drying, grinding to obtain mixture powder, and performing second calcining on the mixture powder in the protection of the inert gas, cooling, and preparing the two-dimensional nitrogen-doped porous carbon nanosheet. The prepared two-dimensional nitrogen-doped porous carbon nanosheet has uniform porosity, good energy storage performance and circulation stability.
Owner:华芯检测(无锡)有限公司

Preparation method of modified manganese oxide material for lithium ion batteries

The invention discloses a preparation method of a modified manganese oxide material for lithium ion battery positive pole materials, which comprises the following steps: 1. preparing manganese source compound and aluminum salt in a mol ratio of 39:1-9:1 into a 0.2-0.5 mol / L water solution, independently preparing carbonate into a 0.2-0.5 mol / L water solution, reacting the two solutions for 4-8 hours by a coprecipiation process while controlling the temperature of the two solutions at -5-10 DEG C, gradually heating to 80-100 DEG C to react for 4-8 hours, filtering, and drying to obtain aluminum-doped precursor manganese carbonate powder; and 2. calcining the obtained precursor manganese carbonate powder at 600-800 DEG C for 2-5 hours to obtain the spherical-ion pore-structure modified manganese oxide of which the particle size is 1-3 mu m. The preparation method disclosed by the invention has the advantages of cheap and accessible raw materials, uniform microstructure and favorable doping effect, and has an auxiliary function on the subsequent synthetic structure of the lithium ion battery positive pole material.
Owner:SHANGHAI INST OF SPACE POWER SOURCES

Preparation method of NiAl/WC composite with high-temperature wear resistance

The invention provides a NiAl / WC composite with the high-temperature wear resistance and a preparation method of the composite. The composite is prepared from raw materials including Ni powder, Al powder and WC powder; the mole ratio of the Ni powder to the Al powder is 1:1; the mass of the WC powder accounts for 5wt%-40wt% of the total mass of Ni-Al-WC mixed powder; the Ni powder has the particle size ranging from 100 meshes to 300 meshes and the purity ranging from 95%-99.5%; the Al powder has the particle size ranging from 100 meshes to 300 meshes and the purity ranging from 95%-99.5%; and the WC powder has the particle size ranging from 100 meshes to 300 meshes and the purity ranging from 95%-99.5%. With the preparation method, high-temperature sintering is not required, so that the obtained composite is uniform in structure, free of pores and high in stability.
Owner:SHANDONG UNIV OF SCI & TECH

Carbon-black-filled polyimide-based compound aerogel material and preparation method thereof

InactiveCN106633169ASimple methodSimple and easy microscopic topographyDielectricFreeze-drying
The invention belongs to the technical field of compound aerogel, and in particular relates to a carbon-black-filled polyimide-based compound aerogel material and a preparation method thereof. The compound aerogel is prepared from the following raw materials: one or more water-soluble polyimide precursor-polyamide acids and one or more carbon black. The preparation method comprises the steps of preparing oxidized carbon black dispersion liquid; preparing polyamide acid-oxidized carbon black hydrogel by means of a sol-gel process; preparing polyamide acid-oxidized carbon black aerogel by means of freeze drying; preparing polyimide-carbon black compound aerogel by means of hot imidization. The raw materials for preparing the polyimide-based compound aerogel are low-cost, and the preparation method is simple and easy to implement; the prepared compound aerogel is uniform in micro-morphology. Furthermore, the prepared polyimide-based compound aerogel has excellent mechanical strength and heat resistance, and a lower dielectric constant, thus being an ideal high-temperature dielectric material.
Owner:FUDAN UNIV

Preparation method of manganese dioxide nanowire

The invention relates to the technical field of nanomaterial preparation, in particular to a preparation method of a manganese dioxide nanowire. The preparation method includes the following steps that potassium permanganate is dissolved in water, an inorganic alkali solution is added, a mixed aqueous solution is formed, the mixed aqueous solution is placed and aged for a period of time, and sol-gel is generated; the sol-gel is stirred and dispersed, inorganic acid is dripped, and the inorganic acid and the sol-gel are fully mixed; the mixture is placed in a hydrothermal reaction kettle and subjected to a hydrothermal reaction for a period of time at a certain temperature; precipitate generated in the reaction is washed and dried, and the manganese dioxide nanowire is obtained. Compared with the prior art, the preparation method has the advantages that the process is simple, operation is easy, few kinds of reagents are needed, reaction conditions are mild, cost is low, and environmental friendliness and cleanliness are achieved, and can be applied to industrialized mass production; the obtained manganese dioxide nanowire is small in size, uniform in microtopography and high in purity and can be applied to the fields of supercapacitors, sensors, environmental pollution remediation and the like.
Owner:SHANGHAI INST OF TECH

Preparation method of CuCl/Cu2O/Cu porous nanosheets and obtained product

The invention discloses a preparation method of CuCl / Cu2O / Cu porous nanosheets and an obtained product. The preparation method of the CuCl / Cu2O / Cu porous nanosheets comprises the steps that copper chloride, NaHCO3 and EDTA-2Na are added into a mixed solvent of glycerol and ethyl alcohol and stirred, so that a transparent solution is obtained; and the transparent solution is subjected to the solvothermal reaction, an obtained product is centrifuged and washed, and thus a finished product is obtained. According to the preparation method of the CuCl / Cu2O / Cu porous nanosheets, by adjusting technological parameters such as a reaction system and solvothermal reaction conditions, grain nucleating and growing processes of CuCl, Cu2O and Cu are controlled under the synergistic effect of a surface active agent, a reducing agent and the like, and thus the CuCl / Cu2O / Cu porous nanosheets with uniform morphology and thicknesses and adjustable apertures are obtained. Adopted raw materials are cheap and extensive, reaction controllability is high, products which are uniform in microtopography, narrow in dimension distribution range and high in yield can be obtained only through the one-step solvothermal reaction, and the preparation method has high application value in the fields such as photocatalysis, catalysis, gas sensitivity and lithium batteries.
Owner:UNIV OF JINAN

ZnIn2S4 sodium ion battery negative electrode material and preparation method thereof

The invention provides a ZnIn2S4 sodium-ion battery negative electrode material and a preparation method thereof. Specifically, a precursor solution is transferred into a 50 mL polytetrafluoroethylene reaction kettle, the reaction kettle is placed in a container filled with inert gas, the inert gas is introduced into the precursor solution for 10-30 min to drive dissolved oxygen in the precursor solution, the influence of oxygen on Zn is avoided, and large-scale ZnIn2S4 particles with good crystallinity and a uniform microflower spherical microstructure are obtained.
Owner:HENAN UNIVERSITY

Preparation method of silica gel modified wood-base silicon carbide ceramic material

The invention relates to a preparation method of a silica gel modified wood-base silicon carbide ceramic material and belongs to the field of preparation of wood-base silicon carbide ceramic materials. The preparation method comprises the steps of respectively weighing a certain mass of wood flour, silica powder and silica gel, calculating the total mass, weighing a certain mass of graphene oxide,uniformly mixing weighed graphene oxide and silica gel weighed in the step 1, adding wood flour and silicon powder, uniformly mixing, putting the mixture into a drying oven, drying so as to obtain afirst mixture, respectively pre-hot-pressing or drying, and carrying out sintering reaction on the obtained sample through program temperature control under the protection of nitrogen, so as to obtainthe silica gel modified wood-base silicon carbide ceramic material, wherein the mass of graphene oxide is 1-5% of the total mass of step 1. The preparation method is simple and convenient and is relatively low in quality change rate and relatively good in corrosion resistance; and by virtue of pre-pressure thermal treatment, the silica gel modified wood-base silicon carbide ceramic material has relatively good electric conductivity.
Owner:NORTHEAST FORESTRY UNIVERSITY

Preparation method of flexible carbon/lanthanum ferrite composite fiber membrane material

The invention discloses a preparation method of a flexible carbon / lanthanum ferrite composite fiber membrane material. The method comprises the following steps of dissolving inorganic ferric salt, lanthanum salt and a filament forming agent in a solvent to obtain a precursor solution; carrying out electrospinning on the precursor solution through an electrospinning technology, and obtaining a carbon / lanthanum ferrite composite precursor fiber membrane with uniform thickness through a roller collector; and annealing the carbon / lanthanum ferrite composite precursor fiber membrane in a nitrogen atmosphere to obtain the flexible carbon / lanthanum ferrite composite fiber membrane material. According to the preparation method, the carbon / lanthanum ferrite precursor fiber membrane material is obtained mainly through the electrostatic spinning technology; the flexible carbon / lanthanum ferrite composite fiber membrane is obtained by controlling the heat treatment atmosphere and the annealing condition; by the method, the preparation process of the carbon / lanthanum ferrite composite fiber membrane is simplified, and the obtained fiber membrane has certain flexibility; in the whole preparation process, raw materials are easy to obtain, the process is simple, and the cost is low; and the universality is very high.
Owner:SHAANXI NORMAL UNIV

Perovskite quantum dot and preparation method thereof

The invention discloses a perovskite quantum dot and a preparation method thereof. The method comprises the steps of: mixing a cesium salt, organic phosphine, a poor solvent and organic amine evenly in an inert atmosphere to obtain a cesium precursor solution; mixing a lead salt, organic phosphine, a poor solvent and organic amine evenly in an inert atmosphere to obtain a lead precursor solution;mixing the cesium precursor solution with the lead precursor solution evenly in an inert atmosphere for nucleation reaction of the cesium ions, lead ions and halide ions dissolved out from the mixed precursor solution to obtain CsPbX3 perovskite quantum dots, the surfaces of which are combined with organic amine, wherein X is Cl, Br or I. Specifically, at least one of the cesium salt and the leadsalt is a metal halide. The CsPbX3 perovskite quantum dot material synthesized by the method has uniform micro-morphology and particle size, high luminescence purity and good batch-to-batch stability,thus being beneficial to application of the material in lighting, photoelectric display and photovoltaic fields.
Owner:TCL CORPORATION

MgO-added 0.45BCTZS-0.55BNT high-energy-storage-density ceramic material and preparation method therefor

The invention relates to a MgO-added 0.45BCTZS-0.55BNT high-energy-storage-density ceramic material and a preparation method therefor. The preparation method comprises the steps of firstly, proportioning BCTZS ceramic powder, BNT ceramic powder and magnesia powder according to the stoichiometric ratio of a chemical formula, i.e., 0.45BCTZS-0.55BNT-xwt%MgO, carrying out uniform mixing, then, carrying out granulating and forming, carrying out heat preservation for 2 to 6 hours at the temperature of 1,150 DEG C to 1,200 DEG C, and carrying out sintered ceramic forming, thereby obtaining the high-energy-storage-density ceramic material, wherein the numeric area of x is 3 to 7. According to the ceramic material and the preparation method therefor, MgO is added into 0.45BCTZS-0.55BNT by adopting a solid-phase method so as to improve the breakdown strength of the 0.45BCTZS-0.55BNT, and thus, the ceramic material with high energy storage density is obtained; and by adding the MgO, the dielectric loss of the ceramic material is effectively lowered, and the grain-boundary resistance is improved. Meanwhile, the diffusion rate of the MgO in ceramics is relatively low, so that excessive MgO is accumulated at grain boundaries, and the growth of crystal grains can be effectively inhibited.
Owner:SHAANXI UNIV OF SCI & TECH

Preparation method of electro-catalytic material VS2 for ENRR

A preparation method of an electro-catalytic material VS2 for ENRR belongs to the field of electro-catalytic nitrogen fixation. The method comprises the following steps: mechanically mixing a precursor, performing microwave hydrothermal treatment on a precursor solution, and performing suction filtration, washing and vacuum drying on solid obtained by the hydrothermal treatment to obtain the VS2. The method is mainly used for preparing the VS2 electro-catalysis nitrogen fixation material, and the problem that the performance of VS2 prepared through a common hydrothermal method is poor when the VS2 is used for ENRR is solved. In addition, compared with vanadium disulfide VS2-x obtained by taking sodium orthovanadate as a vanadium source and thioacetamide as a sulfur source in a hydrothermal mode, pure vanadium disulfide VS2 with +4-valence V is obtained by taking ammonium metavanadate as the vanadium source and thioacetamide in a hydrothermal mode, and the corresponding ENRR performance of the vanadium disulfide VS2 is more excellent.
Owner:BEIJING UNIV OF CHEM TECH

Pretreatment method of polysilicon film texturing for cutting solar cell by diamond wire saw

InactiveCN106340569AUniform suede surfaceApparent weakeningFinal product manufacturePhotovoltaic energy generationPre treatmentMicro morphology
The invention provides a pretreatment method of polysilicon film texturing for cutting a solar cell by a diamond wire saw. The method is characterized in that the a diamond wire saw cutting polysilicon silicon is heated to 500 to 1000 DEG C, the temperature is maintained for 0.5 to 6 hours, and then the temperature of the diamond wire saw cutting polysilicon silicon is slowly and naturally reduced to be under 100 DEG C. According to the method, the diamond wire saw cutting polysilicon silicon is suitable for conventional wet method texturing, the average surface light reflection rate is reduced to a level of 20% to 23%, as shown in Table 1; the texturing surface micro morphology is uniform and round and is not distributed along cutting lines, the cutting mark appearance is reduced remarkably, the processing process is simple, the cost is low, and the method is suitable for large-scale production and application.
Owner:NANCHANG UNIV

Silicon carbide diode and preparation method thereof

The invention provides a silicon carbide diode and a preparation method thereof. The silicon carbide diode comprises a silicon carbide substrate, a plurality of epitaxial layers, a plurality of P-type voltage dividing rings, a plurality of P-type diffusion regions, a Schottky barrier layer, an ohmic contact layer, a back metal electrode, a front metal electrode, silicon dioxide films and polyimide layers; the back metal electrode and the silicon carbide substrate are arranged on the ohmic contact layer; the plurality of epitaxial layers are arranged on the silicon carbide substrate; the silicon dioxide films are arranged at the two ends of the plurality of epitaxial layers; the polyimide layers are arranged on the silicon dioxide films; two ends of the front metal electrode are arranged on the silicon dioxide films; and the Schottky barrier layer is disposed on the plurality of epitaxial layers. The laser beam with specific energy is generated through the laser equipment and faces the injection doped region, so that selective region activation and independent activation depth control are realized, and lattice repair and ion activation conditions in the injection region are met.
Owner:北京绿能芯创电子科技有限公司

Electrostatic spinning synthesis method for Alpha-Fe2O3 rod-shaped structure

ActiveCN109183196AGood technical innovationAdjustable aspect ratioInorganic material artificial filamentsDimethyl formamideElectrospinning
The invention discloses an electrostatic spinning synthesis method for an Alpha-Fe2O3 rod-shaped structure. The method comprises the following steps: mixing ethanol and DMF (Dimethyl Formamide), adding trivalent ferric salt, polyether F127 and pragmoline into a mixture, stirring for dissolving the raw materials, then adding an L-lysine aqueous solution and PVP, and uniformly stirring the raw materials, thereby obtaining a spinning fluid; preparing the spinning fluid into precursor fibers by virtue of an electrostatic spinning method, and calcining the precursor fibers, thereby obtaining a product. By virtue of designing a precursor reaction system and regulating and controlling the calcining system, an Alpha-Fe2O3 rod-shaped structure with adjustable length-diameter ratio is obtained; themethod is simple in preparation process and easy to regulate and control, adopted raw materials are extensive in source and low in price, the product is unform in microcosmic appearance and good in repetitiveness, and has extensive application prospects in the field of gas sensing, catalysis and the like.
Owner:UNIV OF JINAN +1

Method for preparing Sn doped Bi2S3 optical film

The invention relates to a method for preparing an Sn doped Bi2S3 optical film. The method comprises the following steps: adding analytically pure Bi(NO3)3*5H2O into distilled water to obtain a solution A; adding analytically pure Na2S2O3 and trisodium citrate into the A solution to obtain a solution B; adding analytically pure SnCl2*2H2O into the distilled water to obtain a solution C; adding the C solution into the B solution to obtain a solution D; putting the D solution into an electric precipitation device, washing an ITO glass basal plate by ultrasonic in ethanol to be served as a cathode, adopting graphite as an anode and preparing an Sn doped Bi2S3 film on the ITO glass basal plate by a cathode constant-voltage precipitation mode; and airing the prepared film naturally in the airafter finishing precipitation so as to obtain the Sn doped Bi2S3 optical film. The invention adopts an electric precipitation method to prepare the Sn doped Bi2S3 optical film with uniform microscopic appearance. The method has simple equipment and simple and convenient operation without an expensive vacuum device and can obtain the Sn doped Bi2S3 optical film with low cost and high efficiency.
Owner:SHAANXI UNIV OF SCI & TECH

Preparation method of modified manganese oxide material for lithium ion batteries

The invention discloses a preparation method of a modified manganese oxide material for lithium ion battery positive pole materials, which comprises the following steps: 1. preparing manganese source compound and aluminum salt in a mol ratio of 39:1-9:1 into a 0.2-0.5 mol / L water solution, independently preparing carbonate into a 0.2-0.5 mol / L water solution, reacting the two solutions for 4-8 hours by a coprecipiation process while controlling the temperature of the two solutions at -5-10 DEG C, gradually heating to 80-100 DEG C to react for 4-8 hours, filtering, and drying to obtain aluminum-doped precursor manganese carbonate powder; and 2. calcining the obtained precursor manganese carbonate powder at 600-800 DEG C for 2-5 hours to obtain the spherical-ion pore-structure modified manganese oxide of which the particle size is 1-3 mu m. The preparation method disclosed by the invention has the advantages of cheap and accessible raw materials, uniform microstructure and favorable doping effect, and has an auxiliary function on the subsequent synthetic structure of the lithium ion battery positive pole material.
Owner:SHANGHAI INST OF SPACE POWER SOURCES

ZIF-8-derived lithium ion negative electrode material and preparation method thereof

The invention belongs to the technical field of preparation of lithium ion battery electrode materials, and particularly relates to a ZIF-8-derived lithium ion negative electrode material and a preparation method thereof, and the material is prepared by a simple coprecipitation method and a heat treatment process. The preparation method provided by the invention has the advantages of being simple and easy to operate, high in material yield, high in rate, stable in structure, large in particle dispersion coefficient, low in cost, green, environment-friendly and the like, and the obtained ZIF-8-derived lithium ion battery negative electrode material is uniform and controllable in morphology, free of agglomeration phenomenon, large in specific surface area, rich in central active sites, and suitable for industrial production. And when being used as an electrode material, the composite material shows relatively high specific discharge capacity and electrochemical characteristics, and can meet the requirements of preparing a high-performance lithium ion battery electrode material.
Owner:ANHUI UNIVERSITY OF TECHNOLOGY

Rare-earth luminescent nano-material based on aggregation induction effect as well as preparation method and application thereof

The invention discloses a rare-earth luminescent nano-material based on an aggregation induction effect as well as a preparation method and application thereof. The rare-earth luminescent nano-material based on the aggregation induction effect, disclosed by the invention, is a novel rare-earth luminescent and aggregation induction effect (AIE) luminescent coexisting material; the material has a uniform microstructure and the grain diameter of grains is about 32.16nm; the preparation method disclosed by the invention is simple, and an oleophylic rare-earth europium complex luminescent componentand a compound A are introduced and the rare-earth luminescent component is covered with by nanoparticles through a co-assembly method; an aldehyde group on the surface can react with amino with polyethylenimine so that the component can be modified onto the surfaces of the particles; the material has strong dispersity in water; the rare-earth luminescent nano-material based on the aggregation induction effect has a ratio fluorescence detection behavior on hydrogen ions. Furthermore, a detection process can be circularly repeatedly used for at least 10 times through simply regulating the pH (Potential of Hydrogen) value of the solution; the rare-earth luminescent nano-material can be potentially applied to the fields including environment acidity detection, cell acid-base imaging and thelike.
Owner:LUOYANG NORMAL UNIV

Preparation method of strong corrosion-resistant magnesium alloy biological composite material

The invention relates to a preparation method of a strong corrosion-resistant magnesium alloy biological composite material, and belongs to the technical field of biological materials. The technical scheme comprises that a blue algae material is effectively cultured by coating the surface of a magnesium alloy with the blue algae material; the surface of the material is effectively coated by nanoparticles formed after calcination, the surface of calcined carbon black has a large number of oxygen-containing functional groups, the surface of the carbon black is allowed to show negative electricity, a HA (hydroxyapatite) phase is promoted to be precipitated and separated out from a solution in a mineralization process, and a hydroxyapatite composite carbon black coating layer is formed. Therefore, the coated carbon black coating layer can promote the uniform growth of hydroxyapatite, flaky crystals with fine morphology and size are obtained, the micro-morphology of the composite coating layer is more uniform and compact, and the gaps between the flaky hydroxyapatite crystals are much less than the gaps of a coating layer coated by a single layer, so the coating layer shows good corrosion resistance, and can effectively improve the corrosion resistance and use aging performance of magnesium alloy materials.
Owner:NOTTING CHANGZHOU PRECISION MACHINERY

A two-dimensional nitrogen-doped porous carbon nanosheet and its preparation method

The invention relates to the field of new-type flexible electrode materials and in particular to a two-dimensional nitrogen-doped porous carbon nanosheet and a preparation method thereof. The preparation method comprises the following steps: (1) preparing a carbon nanosheet: performing first calcining on a carbon material in protection of an inert gas, cooling, and preparing the carbon nanosheet;(2) preparing a porous carbon nanosheet: adding the carbon nanosheet to oxidized acidic solution and performing an oxidation reaction, preparing the porous carbon nanosheet; and (3) preparing the two-dimensional nitrogen-doped porous carbon nanosheet: adding the porous carbon nanosheet and a surfactant to water, uniformly dispersing, adding a nitrogen-doped material, dissolving, uniformly mixing,after drying, grinding to obtain mixture powder, and performing second calcining on the mixture powder in the protection of the inert gas, cooling, and preparing the two-dimensional nitrogen-doped porous carbon nanosheet. The prepared two-dimensional nitrogen-doped porous carbon nanosheet has uniform porosity, good energy storage performance and circulation stability.
Owner:华芯检测(无锡)有限公司

Preparation method of electrocatalytic material B-VS2 for ENRR

The invention discloses a preparation method of an electrocatalytic material B-VS2 for ENRR, and belongs to the field of electrocatalytic nitrogen fixation. The method comprising the following steps: mechanically mixing precursors, carrying out microwave hydrothermal treatment on a precursor solution, and carrying out suction filtration, washing and vacuum drying on a solid obtained by the hydrothermal treatment to obtain B-VS2. The preparation method is mainly used for preparing the B-VS2 electro-catalysis nitrogen fixation material, and the problem that the stability performance is poor when the boron-undoped VS2 is used for ENRR is solved. Compared with that an active center V<4+> is reduced to V<2+> to lose activity in the process of obtaining vanadium disulfide VS2 by taking ammonium metavanadate as a vanadium source and taking thioacetamide as a sulfur source in a hydrothermal manner, the preparation method has the advantages that B-VS2 is obtained by taking ammonium metavanadate as the vanadium source, taking thioacetamide as the sulfur source and taking boric acid as a boron source in a hydrothermal manner, the V<4+> active center is stabilized by doping boron, and further, the catalytic performance of the ENRR is stabilized.
Owner:BEIJING UNIV OF CHEM TECH

A kind of preparation method of cucl/cu2o/cu porous nano sheet and the product obtained therefrom

The invention discloses a preparation method of CuCl / Cu2O / Cu porous nanosheet and the obtained product. The method is as follows: adding copper chloride, NaHCO3, EDTA-2Na into a mixed solvent of glycerol and ethanol, stirring to obtain a transparent solution, The transparent solution is subjected to solvothermal reaction, and the obtained product is centrifuged and washed to obtain the product. The present invention controls the grain nucleation and growth process of CuCl, Cu2O and Cu by adjusting process parameters such as reaction system and solvothermal reaction conditions, and under the synergistic effect of surfactants, reducing agents, etc., to obtain uniform morphology, thickness and CuCl / Cu2O / Cu porous nanosheets with tunable pore size. The raw materials used in this method are low in price, wide in sources, and highly controllable in reaction. Only one step of solvothermal reaction can obtain products with uniform microscopic morphology, narrow size distribution range, and high yield. Lithium battery and other fields have high application value.
Owner:UNIV OF JINAN

A kind of preparation method and application of lithium hydroxy fatty acid

The invention discloses a preparation method and application of hydroxy fatty acid lithium. The preparation method of hydroxy fatty acid lithium comprises: (1) 60 parts by mass of 12 hydroxystearic acid, 4-6 parts by mass of butanediol Alcohol, the citric acid of 0.4-0.6 mass parts, the deionized water of 500 mass parts, adjust pH to 3-4, add in the autoclave after rotating speed 200-500 turns and stir for 1-2 hours; Described deionized water DO is less than 1mg / L; (2) Add 0.2-0.4 parts by mass of lithium citrate hydrate into the autoclave, heat up to 100°C, stir at normal pressure for 0.5-1 hour, then add 4.4-4.6 parts by mass of hydrogen Lithium oxide, put into the autoclave, after airtight, pass nitrogen protection, stir at 220-240°C, 200-400 rpm for 1-2 hours, cool and filter, and wash with hot water. The hydroxy fatty acid lithium of the invention has a smaller particle size, and can improve the dropping point and anti-friction and anti-wear properties of the prepared lithium-based lubricant.
Owner:BELIKE CHEM

A kind of rare earth luminescent nanomaterial based on aggregation induction effect and its preparation method and application

The invention discloses a rare-earth luminescent nano-material based on an aggregation induction effect as well as a preparation method and application thereof. The rare-earth luminescent nano-material based on the aggregation induction effect, disclosed by the invention, is a novel rare-earth luminescent and aggregation induction effect (AIE) luminescent coexisting material; the material has a uniform microstructure and the grain diameter of grains is about 32.16nm; the preparation method disclosed by the invention is simple, and an oleophylic rare-earth europium complex luminescent componentand a compound A are introduced and the rare-earth luminescent component is covered with by nanoparticles through a co-assembly method; an aldehyde group on the surface can react with amino with polyethylenimine so that the component can be modified onto the surfaces of the particles; the material has strong dispersity in water; the rare-earth luminescent nano-material based on the aggregation induction effect has a ratio fluorescence detection behavior on hydrogen ions. Furthermore, a detection process can be circularly repeatedly used for at least 10 times through simply regulating the pH (Potential of Hydrogen) value of the solution; the rare-earth luminescent nano-material can be potentially applied to the fields including environment acidity detection, cell acid-base imaging and thelike.
Owner:LUOYANG NORMAL UNIV

Ca/Mn co-doped (Gd, Y) AG red fluorescent powder

The invention discloses a Ca / Mn co-doped (Gd, Y) AG red fluorescent powder. A chemical formula of the Ca / Mn co-doped (Gd, Y) AG red fluorescent powder is (Gd0.8-5x / 3Y0.2Ca5x / 3)3(Al1-xMnx)5O12. A synthesis method of the fluorescent powder includes: mixing nitrate solution according to a stoichiometric ratio to obtain salt mother solution, mixing with an ammonium bicarbonate precipitant to obtain suspension, performing centrifuging, washing and drying to obtain a white precursor, and finally calcining to obtain (Gd0.8-5x / 3Y0.2Ca5x / 3)3(Al1-xMnx)5O12 red fluorescent powder. In the prepared fluorescent powder, Ca<2+> and Mn<4+> are co-doped according to a mole ratio of 1:1 to neutralize charge defects caused by replacement of Al<3+> with Mn<4+>, and accordingly the fluorescent powder has excellent fluorescent performances.
Owner:UNIV OF JINAN
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