6816 results about "Ultrasonic dispersion" patented technology

The invention relates to a preparation method of a high purity and high concentration graphene suspension, which comprises the following steps of: reacting natural crystalline flake graphite with a strong oxidizer to obtain graphite oxide; spreading the graphite oxide into a dispersing agent, and obtaining a graphene oxide suspension by ultrasonic dispersion; mixing the graphene oxide suspension with hydrazine hydrate under the protection of nitrogen and reacting at constant temperature under ultrasonic radiation to prepare stable graphene suspension. Compared with the traditional method for preparing the graphene suspension, the method introduces ultrasonic in the reduction process of the graphite oxide. The invention has the following advantages that the prepared graphene suspension has high concentration (higher than 1 mg.mL<-1>), high purity (without influence of surface active agents and other impurities), high dispersionstability (time for stable dispersion is more than 60 days) and the like; the graphene prepared by the method has high electrical conductivity (high than 700 S.m<-1>), less number of layers, is simple and easy to implement, and is very suitable for large scale production in industy.

The invention discloses a preparation method of a graphene/polymer nano composite material, which is characterized by comprising the following steps: adding 0.1-30 parts by weight of graphite oxide into 10-3000 parts by weight of water, and dispersing and exfoliating by carrying out ultrasonic dispersion (the power is 50-500W, and the frequency is 10-100000Hz) at 10-100 DEG C for 15 minutes-5 hours or mechanical lapping for 15 minutes-5 hours or mechanical stirring for 1-48 hours to obtain a graphene oxide water solution; adding the graphene oxide water solution into 100 parts by weight of polymer emulsion of which the solid content is 10-70%; continuing the ultrasonic or mechanical stirring to carry out uniform mixing; demulsifying by adding 1-100 parts by weight of 5-100% demulsifier toobtain a graphene oxide/polymer granular suspension; adding 0.1-100 parts by weight of reducer into the graphene oxide/polymer granular suspension, reducing at 20-100 DEG C for 1-72 hours, filtering,and drying in a drying oven at 20-100 DEG C for 2-72 hours or drying in a vacuum drying oven at 20-120 DEG C under a vacuum degree of 0.1-0.01 MPa for 2-48 hours, thereby obtaining the graphene/polymer nano composite material.

The invention discloses a super-hydrophilic and underwater-super-oleophobic oil-water separation mesh membrane, and a preparation method and an application thereof. According to the method, fabric mesh with a specification of 100-300 meshes is subjected to ultrasonic cleaning, and is air-dried under normal temperature; a hydrophilic polymer water-sensitive agent and a cross-linking agent are dissolved in water according to a ratio of 1:9-9:1; the mixture is well mixed by magnetic stirring, such that a solution with a concentration of 1-99% is prepared; nano-sol is prepared with a sol-gel method; the solution and the nano-sol are prepared into a mixed solution with a concentration of 1-99%, and the solution is well dispersed through ultrasonic dispersion; the mesh is soaked in the mixed solution and is vertically lifted, or the mesh is directly sprayed by using a high-pressure spraying gun; and the mesh is bake-dried, such that the super-hydrophilic and underwater-super-oleophobic oil-water separation mesh membrane is obtained. Contact angles of the super-hydrophilic and underwater-super-oleophobic oil-water separation mesh membrane with water and oil in air are both 0 DEG, and the membrane is super-hydrophilic. Under water, the contact angle of the membrane with oil drops is larger than 150 DEG, and the membrane has an oil drop low adhesion characteristic. The mesh membrane provided by the invention can be used in oil-water mixture separation and oil-containing sewage processing.

The invention discloses a method for preparing nano ceramic fibers, which is implemented by the following steps: 1, preparing 3 to 15 volume percent of 10 to 30 nanometer ceramic nanoparticles, 5 to 30 volume percent of spinnable high polymer, 0.5 to 5 volume percent of dispersant and the balance of solvent, wherein the total volume of the raw materials is 100 volume percent; 2, adding the spinnable high polymer into the solvent, heating the mixture in a water bath with magnetic stirring to obtain solution of spinnable high polymer; 3, adding the ceramic nanoparticles and the dispersant into the solution of spinnable high polymer obtained by the step 2, keeping the temperature of the mixture constant in a water bath, performing dispersion and ultrasonic dispersion, and performing swelling at a constant temperature to obtain ceramic nanoparticle/spinnable high polymer/solvent spinning solution; 4, controlling the electrostatic spinning process parameters of the spinning solution obtained by the step 3 to obtain nano fibers; and 5, sintering the nano fibers at 400 to 1,200 DEG C to obtain nano ceramic fibers.

The invention discloses an electrostatic spinning preparation method of ceramic nanometer composite fibers, comprising the following concrete steps of: firstly, according to volume percentage, weighing 3-10 percent of ceramic nanometer particles with the partilce size of 10-300 nm, 3-20 percent of ceramic precursor, 5-30 percent of spinnable polymer and 40-89 percent of solvent with the total volume of 100 percent; secondly, adding the spinnable polymer into the solvent, heating in water bath and magnetically stirring; thirdly, adding the ceramic precursor into the spinnable polymer solution obtained in the second step, heating in water bath, magnetically stirring and ageing; fourthly, adding the ceramic nanometer particles into the ceramic precursor spinnable solution obtained in the third step, heating at constant temperature in the water bath and forming a spinning solution by carrying out ultrasonic dispersion and constant temperature swelling; fifthly, preparing composite nanometer fibers by the spinning solution according to an electrostatic spinning technology; and sixthly, obtaining the ceramic nanometer composite fibers by sintering the composite nanometer fibers. In the method, raw materials have wide selection conditions and wide optional range.

The invention provides a super-hydrophobic nanometer transparent coating and a preparation method thereof and belongs to the technical field of super-hydrophobic paint. The method includes the steps that firstly, a first category of inorganic nanometer particles are added into an organic solution, and ultrasonic dispersion is performed; secondly, dispersing agents and a second category of inorganic nanometer particles are added, and ultrasonic dispersion is performed so that a dispersion solution can be obtained; crosslinking agents and additives are added in the dispersion solution, ultrasonic dispersion is performed, finally, low-surface energy polymers are added, mixtures are evenly mixed, and transparent and clear super-hydrophobic paint is obtained; the surface of a solid base materials is coated with the transparent and clear super-hydrophobic paint, and the super-hydrophobic nanometer transparent coating is obtained through low-temperature thermal drying and curing. The super-hydrophobic performance of the super-hydrophobic nanometer transparent coating prepared through the method is excellent, the contact angle can be 160 degrees, the rolling angle is 1-7 degrees, the super-hydrophobic nanometer transparent coating can be sprayed to the surfaces of most of common materials, the morphology of the surfaces of the materials are not changed, and the application prospects and the application potency are very wide.

The invention discloses an oxidized grapheme/polyaniline super capacitor composite electrode material and the preparation method and the application thereof. The preparation method comprise the following steps: firstly, adding oxidized graphite to water for ultrasonic dispersion so as to form an oxidized grapheme solution with uniformly dispersed single pieces; at room temperature, dropping aniline to the obtained oxidized grapheme solution for continuous ultrasonic dispersion to from a mixed solution; at a low temperature condition, adding hydrogen peroxide, ferric trichloride and a hydrochloric acid solution dropwise to the mixed solution, and stirring the solution for polymerization; and after the reaction is finished, centrifugating, washing and roasting the obtained mixed solution in vacuum to obtain the oxidized grapheme/polyaniline super capacitor composite electrode material which is used as the electrode material of an electricity storage system of a super capacitor and a battery. The oxidized grapheme/polyaniline super capacitor composite electrode material with good electrochemistry performance is obtained by the method, and the specific capacity of the oxidized grapheme and the polyaniline is greatly improved. In addition, the addition of the oxidized grapheme improves the charge and discharge service life of the polyaniline.

The invention discloses a graphene three-dimensional material as well as a preparation method and an application thereof. The material consists of 10 to 99% of graphene and 1 to 90% of the oxide of manganese, nickel, iron or cobalt. The preparation method comprises the following steps: performing ultrasonic dispersion on graphite oxide to prepare a graphite oxide solution; adding a metal salt solution while stirring or under ultrasonic conditions, and adding a hydrazine hydrate solution; conducting reaction in a drying oven or a hydro-thermal reaction kettle; and then drying to obtain the graphene three-dimensional material. The graphene three-dimensional material is applied to a super capacitor with the capacity of 200 to 800 F/g, or used for making the cathode of a lithium ion battery with the capacity of 300 to 1,400 mAh/g. According to the invention, the preparation process is simple; the prepared graphene three-dimensional macroscopic material has high conductivity and strength; and when being used for the cathode of the lithium ion battery and the super capacitor, the material has high performance.

The invention discloses a flexible nano-cellulose-graphene composite film and a preparation method thereof. The mass fraction of the composite film is composed of: graphene 0.1%-90%, nano-cellulose 10%-99.9%, and the preparation steps are as follows: : (1) Prepare a graphene oxide dispersion with a concentration of 0.05-5 mg/ml and a nano-cellulose dispersion with a concentration of 0.05-5 mg/ml, ultrasonically disperse for 1-2 hours, and mix to obtain a concentration of 0.05-5 mg/ml The first dispersion liquid of nanocellulose-graphene oxide; (2) add reducing agent in the first dispersion liquid, heat up, stir, stir evenly, obtain the second dispersion liquid of nanocellulose-graphene; (3) The above-mentioned second dispersion liquid is subjected to centrifugal degassing, and then vacuum-filtered to form a composite film, and the composite film is transferred to an oven, and vacuum-dried to obtain a flexible nanocellulose-graphene composite film. There will be no agglomeration between the graphene sheets in the composite film, and its thermal conductivity in the parallel direction is ≥2W·m ^‑1 ·K ^‑1 , vertical thermal conductivity ≤0.3W·m ^‑1 ·K ^‑1 , Thermal conductivity anisotropy ratio ≥ 5.

The invention relates to a method for preparing a metal liquid mixed with particles which has high heat transferring performance. The method comprises the following steps: a. particles as a solute and liquid metal as a solvent are mixed to form the liquid metal mixed with the particles; the ratio of mass portions of the particles to the liquid metal is between 1 to 0.1 and 1 to 99; and b. the liquid metal mixed with the particles is subjected to mechanical stirring and ultrasonic dispersion in order that the particles in the liquid metal are evenly dispersed, thereby obtaining the metal liquid mixed with the particles. Through the method, the prepared metal liquid mixed with the particles has high thermal conductivity.

The invention relates to a method for preparing multi-layer graphene, and belongs to the technical field of carbon materials. The multi-layer graphene is prepared from expanded graphite serving as a raw material through ultrasonic dispersion, solid-liquid separation and drying. The thickness of the multi-layer graphene prepared by the method is between 1 and 10nm; the number of layers is between 2 and 20 layers; and the aperture is mainly between 6 and 50nm. The multi-layer graphene has the characteristics of high electrical conductivity, high heat conductivity, high electromagnetic wave absorptivity, wear resistance and the like. The method has the advantages of simpleness, convenient operation and low production cost, capability of reducing production energy consumption, no three wastes emission, environmental friendliness and convenient popularization and application. The multi-layer graphene prepared by the method can be used as the electrode materials of batteries and super capacitors, can also be used as the conductive agents of high molecular materials, ceramic materials, silicate materials and the like, and can also be used as the conductive agents of lithium batteries, alkaline batteries and nickel-metal hydride batteries.

The invention discloses graphene-organic acid doped polyaniline composite material and a preparation method thereof. The preparation method includes the following steps: adding graphite oxide to dispersing agent for ultrasonic dispersion to form evenly dispersed graphene oxide liquid mixture; adding aniline monomer to the liquid mixture obtained in the first step for further dispersion under room temperature to form liquid mixture, and then blending for certain time; gradually dripping oxidizer and organic doping acid to the liquid mixture obtained in the second step, and blending for polymerization; centrifuging the liquid mixture obtained in the third step, and washing to get graphene oxide-polyaniline composite material; adding concentrated alkaline to the water suspension of the graphene oxide-polyaniline composite material, heating and blending for reaction; and centrifuging the mixture obtained in the fifth step and washing to get graphene-polyaniline composite material. The invention takes the advantage of the big specific surface area of graphene oxide and the capability of the graphene oxide for absorbing aniline on the surface thereof in on organic system to form sandwiched polyaniline/ graphene oxide- polyaniline compound through polymerization.

The invention relates to a carbon fiber emulsion sizing agent improved by a carbon nano tube and a preparation method of the carbon fiber emulsion sizing agent. The carbon fiber emulsion sizing agent comprises a carbon fiber sizing agent, the carbon nano tube, a dispersing agent and a solvent. The preparation method comprises the following steps of: 1, preparing the carbon fiber sizing agent; and 2, adding the carbon fiber sizing agent into the solvent to prepare a sizing working solution, mixing the carbon nano tube and the sizing working solution, performing ultrasonic treatment for 1 to 4 hours at the power of 300 to 600w, adding the dispersing agent, and performing ultrasonic dispersion for 2 to 4 hours to obtain the carbon fiber emulsion sizing agent improved by the carbon nano tube. The carbon fiber emulsion sizing agent has favorable stability, the post processability of carbon fiber can be improved after being processed by the emulsion sizing agent, the interfacial bond strength between the carbon fiber and substrate resin can be enhanced, the shear strength among layers is enhanced, and the performance of a composite material is improved to a certain extent. Moreover, the preparation method is simple, low in cost and environment-friendly.

The invention relates to graphene-oxide-modified phenolic-resin-based ultrafine porous carbon fiber and a preparation method thereof. The diameter of the fiber is in a range of 0.3-1.7mum, and the specific surface area of the fiber is 500-900m<2>/g. The fiber has a porous structure which is formed by microporous mainly. Micro-pore volume is 0.20-0.50cm<3>/g, and surface oxygen atomic ratio is lower than 10%. The preparation method comprises the steps that: graphene oxide is added into an organic solvent and is subjected to ultrasonic dispersion, such that a graphene oxide solution is formed; termosetting phenolic resin and a high-molecular-weight linear polymer are added into the graphene oxide organic solution, and are completely dissolved by stirring; the mixed solution is spun into composite fiber, and solidification and carbonization are carried out, such that porous phenolic-resin-based carbon/graphite oxide composite ultrafine fiber is obtained. The sources of adopted raw materials are rich. The prepared composite fiber has the advantages of high structural stability, good flexibility, developed pore structure, controllable surface oxygen content, and suitability for practical application.

The invention relates to a preparation method of a graphene and manganese dioxide nanocomposite material, comprising: (1) stirring and mixing graphite, potassium nitrate and concentrated sulfur evenly, adding potassium permanganate, and reacting at 30-40° C. for 20-40 minutes , add deionized water at room temperature, add hydrogen peroxide after reacting for 15 to 30 minutes to obtain graphite oxide; (2) disperse the above graphite oxide in water, add hydrazine hydrate, and react at 95°C for 1 to 24 hours to obtain graphene (3) ultrasonically disperse the graphene in a saturated potassium permanganate solution, add acid, and react at 60-80° C. for 1-5 hours to obtain graphene and manganese dioxide nanocomposite material. The invention has the advantages of simple reaction, easy control, convenient operation and simple process; the obtained composite material has broad application prospects and can be used for catalysts, biosensing materials, electrode materials of lithium ion batteries and supercapacitor electrode materials, and the like.

The invention relates to a transparent heat insulation coating material, the preparation method and the application thereof. The material is made from the raw material of lanthanum hexaboride/tin indium oxide or lanthanum hexaboride/tin antimony oxide, by the steps of pretreating by ultrasonic dispersion, and grinding to prepare nanometer slurry with heat insulation function, wherein the nanometer slurry has particle sizes mainly between 10nm and 200nm, the average particle size between 50nm and 120nm, and superior dispersion stability; mixing the nanometer slurry with film forming substance, auxiliary agent and solvent, to obtain the transparent heat insulation coating material. The coating material can obstruct more than 80% of infrared light, has a visible light transmittance above 60%, achieves excellent transparency and sunshine energy shielding effect; can be directly coated on transparent glass, polycarbonate, synthetic glass and polyester; and achieves the aims of energy conservation and heat insulation.

The invention discloses a magnetic carbon nanotube composite material and a preparation method and an application thereof. The preparation method comprises the following steps: adding FeCl3.6H2O to an ethylene glycol solution; then adding anhydrous sodium acetate and polyethylene glycol; adding a carboxylated multiwalled carbon nanotube; performing ultrasonic dispersion; adding hexamethylenediamine or ethanediamine; heating to 200-300 DEG C for reaction for 8-24h; and washing and performing vacuum drying to prepare the amino-modified magnetic Fe3O4-carbon nanotube composite material. The amino-modified magnetic Fe3O4-carbon nanotube composite material prepared by the invention is of nanoscale and superparamagnetism, can be stably dispersed in solutions, and can be quickly separated and enriched through a simple action of a magnetic field. As an adsorbent, the material is large in superficial area and has various active groups on the surface. The material can adsorb pigments from complex substrates through pi-pi electron interaction and hydrophobic effect of the carbon nanotube and can adsorb compounds such as organic acids and phenols through weak anion exchange effect of amino groups on the surfaces of magnetic nanoparticles.

Provided is a preparation method of silver nanowires. The preparation method of the silver nanowires includes the following steps: adding water-solubility silver salt and dispersing agents into aqueous solution comprising polyhydroxy liquid organic matters, and obtaining mixed liquor after ultrasonic dispersion; adding water-solubility halide into the mixed liquor, and obtaining reaction mother liquor after dissolving; reacting the mother liquor under 100-190 DEG C for 10-60 minutes, and obtaining mixtures; and collecting sediment after centrifugation of the mixtures, drying the sediment after washing of the sediment and obtaining the silver nanowires. The preparation method of the silver nanowires is short in preparation time.

The invention provides a graphene modified high-heat-conductivity aluminum-based composite material and a powder metallurgy preparation method thereof. The material comprises reinforced grains and an aluminum substrate, wherein the composite boundary of the reinforced grains and the aluminum substrate contains high-heat-conductivity graphene nanosheets. The method comprises the following steps: (1) soaking the reinforced grains with a strong acid solution, subsequently washing with deionized water till being neutral, drying, and removing the surface impurities, thereby obtaining activated reinforced grains; (2) adding the activated reinforced grains into a graphene dispersion liquid, mechanically stirring or performing ultrasonic dispersion, and wrapping the graphene nanosheets on the surface, thereby preparing the graphene modified reinforced grains; and (3) mixing the graphene modified reinforced grains with the aluminum substrate powder, pressing into blanks, and sintering, thereby preparing the graphene modified high-heat-conductivity aluminum-based composite material. The composite material provided by the invention is good in chemical stability, high in thermal conductivity and can be used as a heat management material of a large-power semiconductor device.

The invention discloses a visible light responsive pucherite-graphene composite photocatalyst and a preparation method thereof. The composite photocatalyst is prepared by compositing pucherite and graphene according to the mass ratio of (1:2)-(1:5). The preparation method comprises the following steps of: putting graphite oxide into a mixed solution of water and ethanol for ultrasonic dispersion,respectively adding bismuth nitrate and ammonium metavanadate into ethanol for stirring, and finally mixing the three systems and regulating the pH to be greater than 7; then, transferring the mixed system into a hydrothermal kettle for reacting; and after the reaction is finished, centrifugally separating, washing and drying the product to obtain a leaf-shaped pucherite-graphene composite photocatalyst. In the invention, by using graphene as a template, the leaf-shaped pucherite-graphene composite photocatalyst is prepared by a hydrothermal synthesis method. The pucherite-graphene composite photocatalyst prepared by the method disclosed by the invention has better application prospect and economic benefit in the aspect of sewage treatment.

The invention relates to a grapheme reinforcing agent-containing reinforced wear-resistant material and a preparation method thereof. A composition of the wear-resistant material comprises grapheme, polyolefin and a coupling agent, wherein the weight ratio of the grapheme to the polyolefin is 0.5:99.5-10:90; and the using amount of the coupling agent is 0.5-5 percent of the mass of the grapheme. The preparation method of the wear-resistant material comprises the following steps of: putting grapheme and the coupling agent which is dissolved into acetone or absolute ethyl alcohol serving as a solvent into a container; dispersing with ultrasonic waves; removing the solvent to constant weight; uniformly mixing with the polyolefin; and fusing in an internal mixer at the temperature 190-230 DEGC, and blending for 7-20 minutes. By adopting the method disclosed by the invention, the wear performance and mechanical property of a polyolefin material are enhanced remarkably, and the applicationfield of the polyolefin material is expanded.

The invention discloses a method for preparing nitrogen-doped graphene with high nitrogen doping amount. The method comprises the following steps: (1) dispersing of graphene; (2) ultrasonic dispersion; (3) microwave heating; and (4) filtering and drying. The nitrogen doping amount of the nitrogen-doped graphene prepared by the method disclosed by the invention is 10%-15.0%, the density of free carriers in graphene is greatly increased by the high nitrogen doping amount, the interaction of graphene and metal is enhanced, no oxidation pretreatment is carried out, no toxic solvent is used in the reaction process, reactants are simple in component, reaction conditions are mild, and the prepared nitrogen-doped graphene has excellent electrochemical property and can be used for preparation of new energy materials such as lithium ion battery, lithium-air battery, super capacitor electrode material and fuel cell oxygen reduction catalysts. According to the method disclosed by the invention, a high-pressure kettle is heated by using microwaves without high temperature; the method is low in energy consumption, is carried out in an airtight environment and therefore hardly causes environment pollution; in addition, the method is simple in process and convenient to operate and needs less production equipment, thus, the cost is further reduced.

The invention discloses a method of electrolytically extracting and detecting fine inclusions in steel, belonging to the technical field of metal physical research methods. The method comprises the following technical steps of: using an organic electrolyte to carry out electrolysis on a steel sample; after electrolysis, washing the electrolyte mixed with the inclusions by absolute ethyl alcohol, and carrying out magnetic separation on the electrolyte by a magnet; separating the electrolyte after magnetic separation and collecting the inclusions by adopting a method of centrifugation by a centrifugal machine; putting the collected inclusions into a solvent easy to volatilize, carrying out ultrasonic dispersion on the inclusions by an ultrasonic cleaner, and then dripping a solution after ultrasonic dispersion on a carrier drop by drop by a trace pipette; and after the solvent volatilizes, putting the carrier which is distributed with the inclusions into a scanning electron microscope to analyze. The method has the advantages that the fine inclusions can be extracted in an undamaged way, the obtained inclusions are good in dispersion under a field of view of the scanning electron microscope, the shapes of the inclusions are perfect, and a good space statistic analysis result can be obtained so as to supply accurate data for a product.