99results about How to "The production process is fast" patented technology

The present invention relates to film on the surface of medical titanium-base metal material and its sand blasting-micro arc oxidizing compounding process. Through the first surface sand blasting treatment of titanium or titanium alloy material and the subsequent micro arc oxidizing in electrolyte solution containing phosphate radical ion and calcium ion and with the titanium or titanium alloy material as anode, stainless steel or titanium as cathode and DC power source or DC pulse power source, one bioactive film is in-situ formed on the surface of the titanium or titanium alloy material. The bioactive film of rough porous hydroxyapatite has surface roughness Ra of 2-4.5 micron, no interface with the substrate, elastic modulus reaching that of bone and excellent bioactivity, and may be used as the substitute for femur, hip joint, tooth root, etc. The bioactive film has optimized combination strength, stability and bioactivity.

The invention discloses bridge coarse aggregate active powder concrete and a preparation method thereof. The coarse aggregate active powder concrete comprises, by weight, 100 parts of cement, 20-60 parts of blending materials, 2-10 parts of interface modifying agents, 60-120 parts of fine aggregates, 40-120 parts of coarse aggregates, 10-60 parts of fibers and 15-30 parts of water. Under conventional curing processes such as natural conditions, the coarse aggregate active powder concrete has super-high compressive strength, bending tensile strength and tensile strength and bonding strength andlow contraction performance and further has high elasticity modulus, anti-fatigue performance and durable performance and excellent construction performance, dead weight and shrinkage and creep influence of a bridge can be reduced, and the span, the structural stiffness and the bearing capacity of the bridge can be remarkably improved, and the service life of the bridge is prolonged.

The invention discloses a gold micro-nano composite structure array and a preparation method thereof. The array is a gold bowl array or a gold hollow sphere array disposed above a gold film covered on a substrate, wherein the diameter of a gold bow opening is from 500 nanometers to 10 micrometers, a bowl wall is composed of gold rods, the lengths of the gold rods are 100-1000 nanometers, the diameters of the gold rods are 50-400 nanometers, the inner diameter of a gold hollow sphere is from 500 nanometers to 10 micrometers, a sphere casing is composed of gold particles with diameters of 50-600 nanometers, and the thickness of the gold film is 5-25 nanometers. The preparation method includes sputtering a layer of the gold film on the substrate, placing a single layer colloidal crystal template which is composed of polystyrene colloidal spheres with diameters from 500 nanometers to 10 micrometers on the substrate which is covered with the gold film, then placing the substrate covered with the gold film and the colloidal crystal template into a chloroauric acid solution with concentration of 0.3-0.7g/L, using the solution with the substrate as a working electrode, subjecting the mixture to electro-deposition for 2-8 hours under the deposition electric current density of 0.03-0.05mA/cm<2> or 0.15-0.45mA/cm<2> to obtain a complex array, and placing the complex array in a dichloromethane solution for to removing the polystyrene colloidal spheres to obtain target products. The gold micro-nano composite structure array can be used as a surface enhanced raman scattering active substrate.

The invention relates to a method for preparing a titanium dioxide layer with a multi-level pore structure on the surface of medicinal titanium. The method provided by the invention comprises the following steps of: performing anode oxidation of a direct-current slow uniform-speed current raising mode on the medicinal titanium in acetic electrolyte, and performing secondary anode oxidation of a direct-current constant voltage mode in sulfuric acid or sodium acetate electrolyte to obtain the titanium dioxide layer with the multi-level pore structure, wherein the large-pore structure consists of staggered groove structures, the widths of grooves are 20 to 30 microns, the small-pore structure comprises submicron micropore structures densely distributed on the whole film, and the aperture is between dozens of and hundreds of microns. The method is simple and rapid, has simple and convenient operation, and is expected to become a surface modification method for medicinal titanium metal in the field of orthopedics, dentistry or plastic surgery.

The invention discloses equipment and a process for industrially producing containers by using moso bamboo. The equipment comprises a moso bamboo cutter, a moso bamboo joint beating machine for beating internal joints of segment bamboo, a high-temperature segment bamboo softening container, a segment bamboo washing device, a segment bamboo thermal insulation device, a precision moso bamboo rotarycutter for rotationally cutting the segment bamboo, a bamboo sheet length control device, a bamboo sheet drying machine for drying bamboo sheets, a double-sided gluing machine for coating glue on thebamboo sheets, and a bamboo sheet hot-press section forming machine. The process comprises the following steps of: cutting the moso bamboo, beating the internal joints of the segment bamboo, softening the segment bamboo at high temperature, washing the segment bamboo, performing thermal insulation on the segment bamboo, rotationally cutting the segment bamboo into the bamboo sheets, drying the bamboo sheets, coating glue on the bamboo sheets, hot-pressing a plurality of bamboo sheets coated with the glue to obtain bamboo sheet sections meeting the requirements on thickness and dimension, and respectively moulding the bamboo sheet sections in a square container moulding mould, a bamboo sheet cylindrical container moudling mould and a once-setting mould for moulding containers to obtain square containers, cylindrical containers, round or square discs and the like without abutted seams.

A process for extracting the active component from the root, stem and leaf of arthicoke includes such steps as crushing, decocting in water or thermal reflux in alcohol 3 times, collected liquid, depositing, and concentrating its supernatant. It can be mixed with sweetening agent, excipient, filler and coloring agent to prepare medicines or health-care food for lossing weight, protecting liver and galladder, regulating gastrointestinal function, and relaxing cardiovascular disease.

The invention discloses a method and a device for preparing porous ceramic micro beads. The method comprises the following steps of: mixing an organic monomer and a crosslinking agent with water according to a certain proportion for dissolving, adding ceramic powder and a dispersing agent into a solution, and performing ball milling to obtain a ceramic suspension with high solid phase content and low viscosity; adding a foaming agent, an initiator and a catalyst into the suspension for stirring to obtain water-based stable foam ceramic slurry; and continuously injecting the water-base slurry into an oily medium of a certain temperature by using the device for preparing the porous ceramic micro beads to form foam slurry spheres, floating and curing into porous ceramic micro bead blanks in the oily medium, collecting, cleaning, drying and sintering to obtain a porous ceramic micro bead product. The invention further discloses a device for preparing the porous ceramic micro beads. The device comprises a micro bead forming tower and an injection gun, and can be used for realizing continuous automatic injection and generation of spheres. The device has universality, and can be used for realizing large-scale continuous production of porous ceramic micro beads which are of different systems and are 0.3-4.0 millimeters in diameter.

The invention relates to a titanium oxide composite coating and a preparation method thereof. The titanium oxide composite coating comprises a porous titanium oxide coating formed in situ on the surface of a titanium-based metal base material by virtue of a micro-arc oxidation technique, and ferric oxide nanoparticles mixed with the porous titanium oxide coating by virtue of a plasma-immersion ion implantation technique, wherein the content of the iron element in the titanium oxide composite coating ranges from 1% to 15%. The invention also provides a method for preparing the titanium oxide composite coating, and the method comprises the steps of (1) forming the porous titanium oxide coating in situ on the surface of the titanium-based metal base material by virtue of the micro-arc oxidation technique, and (2) implanting iron ions into the titanium oxide coating by virtue of the plasma-immersion ion implantation technique to form the ferric oxide nanoparticle modified titanium oxide composite coating.

The invention discloses a method for preparing porous nanometer graphite and belongs to the field of research on nanometer carbon materials. The method comprises the following main steps: preparing a water-soluble carbon source as a raw material, an auxiliary agent and iron salts according to an appropriate ratio into a solution and heating; evaporating, concentrating and reacting the solution to obtain carbon-containing precursor powder, reacting the precursor for 0.5-5 hours at 600-1300 DEG C under a certain atmosphere to obtain a reaction product, and washing the reaction product with acid to obtain porous nanometer graphite. The method is simple in operation and low in cost and is conductive to industrial production; the obtained product is high in degree of graphitization, has a porous structure and can be widely applied in such fields as lithium ion cells, field emission materials and super capacitors.

A high heat conduction and high attenuation backing material for ultrasonic phased array probe is made from lutecium oxide, alumina, a tungsten compound material and an epoxy adhesive and is characterized in that the epoxy adhesive is prepared by mixing epoxy resin E-54 and triethanolamine; the tungsten compound material is prepared by mixing rubber and a tungsten powder; and the alumina accounts for 10.48-53.04wt% of the backing material. A manufacturing method of the backing material comprises the following steps of: (a) mixing the epoxy resin E-54, lutecium oxide, alumina and the tungsten compound material with stirring, wherein the epoxy resin E-54 accounts for 6.22% the total weight of the backing material and alumina accounts for 10.48-53.04wt% of the backing material; (b) adding triethanolamine which accounts for 0.95% the total weight of the backing material into the above composite particles with stirring; (c) putting the composite particles into a die, and extruding the composite particles into the required backing material by the use of a powder pressing machine; and (d) putting the pressed backing material into an air-blasting heating oven of 65 DEG C for heating-curing. The thermal conductivity of the backing material is 1.782W/(m.k), its specific acoustic impedance is 8.42*106Pa.s/m and its acoustic attenuation coefficient at 5MHz is 294.4dB/cm. The backing material has high thermal conductivity and high attenuation. In addition, the sensitivity and resolution of the phased array probe produced by the use of the backing material can satisfy the requirement for application.

The invention relates to a preparation method of a bio oil-phenol-methanal copolycondensation resin wood adhesive, belonging to the technical field of fine chemistry and high polymer materials, which comprises the following steps of filtering and refining bio oil to prepare the refined bio oil; adding sulfur and sodium hydroxide solution to the refined bio oil; stirring, heating and reacting to prepare the modified bio oil; and adding phenol and a catalyst to the modified bio oil to prepare the adhesive after reacting. In the method of the invention, the bio oil is taken as a substrate to synthesize the adhesive for wood, and the content of the bio oil is 50 to 60% of the total content of the adhesive. The prepared adhesive has the advantages of high mechanical strength, good waterproof performance and aging resistance, and can be used for preparing the products in high accessories of outdoor stage plywood, particle boards, fiberboards, layer base materials and the like. Moreover, thepreparation technology for pyrolyzing the bio oil wood adhesive is simple and fast, and the resins have the advantages of strong adhesion performance and long storage life.

The invention discloses a flexible texture coating which comprises the following components according to percentage by mass: 5-10% of water, 0.1-0.3% of anti-mildew anti-algae agent, 0.05-0.15% of preservative, 0.1-0.3% of dispersing agent, 0.05-0.15 of wetting agent, 0.02-0.07% of defoaming agent A, 7.5-11.5% of 600-mesh heavy calcium carbonate power, 10-15% of titanium dioxide, 1.5-3.0% of ultra-fine aluminium silicate, 10-15% of emulsion A, 15-20% of emulsion B, 10-12% of X1-X2-mesh heavy calcium stone tablet, 10-12% of X3-X4-mesh heavy calcium stone tablet, 13-15% of X5-X6-mesh heavy calcium stone tablet, 0.05-0.1% of defoaming agent B, 0.5-0.15% of solvent HA, 1-3% of solvent HB, 0.2-0.3% of cellulose A, 0.1-0.2% of cellulose B, 0.5-0.7% of thickening agent and 0.05-0.15% of PH value adjusting reagent. The flexible texture coating of the invention has the advantages of bridging slight crack, rich forms and colors and environmental protection; the preparation method of the invention has simple, easy and fast process.

The invention discloses an efficient environment-friendly low-temperature composite phase change cold accumulating agent. The cold accumulating agent is prepared from the following components in percentage by mass: 5-11 percent of potassium chloride, 10-15 percent of sodium chloride, 0.1-0.6 percent of citric acid, 1-1.5 percent of sodium tetraborate, 0.5-2 percent of guar gum and 70-83.4 percent of water. The invention further discloses a method for preparing the efficient environment-friendly low-temperature composite phase change cold accumulating agent, and application of the efficient environment-friendly low-temperature composite phase change cold accumulating agent in the field of storage and fresh preservation. Compared with a traditional cold accumulating agent preparation process, the process has the characteristics of convenience and rapidness, the prepared cold accumulating agent is transparent or translucent gel, and has the characteristics of safety, no pollution, efficiency, large latent heat of phase change and small condensate depression. Experiments prove that the phase-change temperature is between minus 21 and minus 24 DEG C, and the latent heat of phase change is 280-320kJ/kg.

The invention relates to a method for reducing the protein content in soybean dietary fiber. The method comprises the following steps: feeding water into dried bean dregs, adjusting the pH, then feeding neutral protease into the dried bean dregs, carrying out heat preservation at the temperature of 60 DEG C, and oscillating; centrifuging the oscillated composition for 10 minutes at the rotating speed of 3000 revolutions/ minute; removing supernatant to obtain lower sediment, washing the sediment by water, adjusting the pH, then feeding pectinase, hemicellulase and cellulase, carrying out heat preservation at the temperature of 60 DEG C, and oscillating; and separating fiber from supernatant by centrifugation, washing and then purifying to obtain the soybean dietary fiber. The preparation technology is simple and fast; the soybean dietary fiber prepared by the method is high in fiber purity, and does not easily have the phenomena of moisture absorption and color change; and the storage life of the soybean dietary fiber can be prolonged. After the soybean dietary fiber is treated by the method, the protein content in the soybean dietary fiber is reduced to about 6% from about 20%.

The invention discloses a display device and a manufacturing method of the display device. The display device comprises a frame, an organic light-emitting diode panel, a light-transmitting element and a glue material. The organic light-emitting diode panel is arranged in the frame. The light-transmitting element is arranged on the organic light-emitting diode panel. The glue material is arranged between the organic light-emitting diode panel and the light-transmitting element and between the organic light-emitting diode panel and the frame in a filling mode.

The invention discloses a preparation method for the non-alkaloid part of sophorae tonkinensis, which belongs to the technical field of Chinese medicine. The preparation method is as follows: ethanol is added into water regurgitation extract of the sophorae tonkinensis; insoluble substance is precipitated and filtered; filtrate is condensed and carries out column chromatograph separation by the strong acid cationic resin of crosslinked polystyrene series; the filtrate is eluted by water; eluted water is collected and condensed to ointment; and the ointment is decompressed and dried to obtain the non-alkaloid part. The non-alkaloid part contains carbohydrate, organic acid, phenols and saponin and son on. The preparation process of the invention is easy and quick and the cost of preparation is low. In addition, the quality of various substances of the obtained product is stable and controllable. The non-alkaloid part is applied for reducing enzyme and protecting liver, and offers substance base for seeking more efficient non-alkaloid active components.

The invention relates to a preparation method of functionalized polymer microspheres, belonging to the technical field of preparation of functional polymers. According to the preparation method, an oil-soluble polyfunctionality acrylate monomer, polyethyleneimine and a photoinitiator are used as raw materials, wherein the weight ratio of the polyfunctionality acrylate monomer to the photoinitiatorto the polyethyleneimine to a water solvent is equal to 100 to (1-5) to (5-20) to (500-2000). After the system is uniformly mixed, emulsification is firstly carried out under the action of a high-speed disperser, and ultraviolet light irradiation is performed after the emulsification is finished, so that polymer microspheres of polyfunctionality acrylate are obtained; after that, the polymer microspheres and polyethyleneimine are subjected to a Michael addition reaction, so that the functional polymer microspheres having surfaces modified by active primary amino groups and secondary amino groups. The functional macromolecular microspheres, which are prepared by the method and have aminated surfaces, are low in reaction energy consumption, and the reaction rate and the reaction yield can be adjusted by means of time. The particle sizes of the polymer microspheres can be adjusted within a range of 2-100mu m. The polyethyleneimine not only serves as a stabilizer in a formation process ofthe microspheres, but also can be used as a modifier in a microsphere modification process.