73 results about "Mg composite" patented technology

This invention relates to a method for preparing catalyst for ethylene homopolymerization or copolymerization with other alpha-olefins. The catalyst comprises at least one Mg composite, at least one Ti compound, at least one organic alcohol compound, and at least one Si compound. The general formula of the Si compound is R1xR2ySi (OR3) z, where R1 and R2 are alkyl or halogen; R3 is alkyl; x is 0-2; y is 0-2; z is 0-4; x + y + z = 4. The catalyst has such advantages as high catalytic activity, high hydrogen sensitivity and narrow particle size distribution of polymer. The catalyst is suitable for slurry polymerization of ethylene, and combined polymerization process where catalyst with high activity is needed.

The invention provides a method for preparing nanoporous silicon with industrial silica powder as a raw material. Silica powder and magnesium powder are subjected to alloying treatment, a precursor Mg2Si/Mg composite material is prepared, then dealloying treatment is carried out, finally the prepared product is subjected to acid pickling, centrifugation and drying, and nanoporous silicon is prepared. The method can raise the utilization rate of industrial silica powder, achieves resource utilization of silica powder, raises the additional value of silica powder, and has characteristics of wide raw material sources, low cost and simple technology operation. The prepared nanoporous silicon has characteristics of uniform pore size distribution, large specific surface area and the like, and has wide application prospects.

The invention discloses a method for smelting a steel plate with the excellent performance in a high-heat-input-welding heat affected zone. The method sequentially includes the steps of molten steel pretreatment, combined-blowing converter steelmaking, LF refining, RH vacuum refining, alloy cored wire feeding and continuous casting. According to the method, the content of oxygen in molten steel and the adding conditions of key alloy materials at key stations are controlled, the content of Ti, the content of O, the content of Mg and the content of Zr in the steel meet the design requirements accordingly and can meet the conditions that Ti/O is larger than 5 and smaller than 12, (Mg+Zr)/(Ti+Al) is larger than 0.02, and one or two kinds of a large quantity of Ti-Mg composite-oxide inclusions, a large quantity of Ti-Zr composite-oxide inclusions and a large quantity of Ti-Mg-Zr composite-oxide inclusions with the size smaller than 1 micron are contained in the steel accordingly; in addition, the mass percents of chemical compositions of the inclusions meet the conditions that the mass percent of Ti is larger than 2% and smaller than 40%, the mass percent of Mg is larger than 2% and smaller than 30%, the mass percent of Zr is larger than 2% and smaller than 30%, and the mass percent of O is larger than 5% and smaller than 50%; and the areal density is larger than 300 per mm<2>. Due to the inclusions, growth of austenite crystal grains of the welding heat affected zone can be effectively pinned; and meanwhile nucleus forming of needle-shaped ferrite in the grains is promoted, and therefore the excellent performance in the high-heat-input-welding heat affected zone is guaranteed.

The invention relates to a method of in-situ preparing TiB2 granule strengthening Mg-based composite material in the composite material technical field. The steps are that: powder of K2TiF6, KBF4 and Na3AlF6 are mixed uniformly and then put into a kiln for drying, thus obtaining waterless powder. Aluminum ingot is melted in a resistance furnace with heat preservation and uniformity; the waterless powder after dried is added to the melting Al melt liquid by batch and then is stirred with a graphite disc, and scum on the surface of the melt liquid is removed after stirred and stewed, thus obtaining TiB2-Al intermediate alloy; magnesium alloy is smelted with the protection of SF6 and CO2 mixing gas, and flame retardant element beryllium is added; the TiB2-Al intermediate alloy is added into the magnesium alloy melting solution slowly, stirred, stewed and cast. The technology of the invention is comparatively simple, has low cost, and the density of TiB2/Mg composite material is between 1.8-2.0g/cm<3> and tensile strength thereof is increased by more than 60 percent than base alloy.

The invention discloses a degradable lamellar Zn-Mg composite material and a preparation method thereof. The outer layer of a lamellar medical metal composite material is made of pure zinc or zinc alloy, and the core part of the lamellar medical metal composite material is made of pure magnesium or magnesium alloy; the ratio of zinc or zinc alloy and magnesium or magnesium alloy is calculated according to volume percentage, zinc or zinc alloy accounts for 20%-50% of the total volume of the material, and the balance is magnesium or magnesium alloy. The lamellar composite material is prepared bycombining layered casting with nested extruding. The degradable lamellar Zn-Mg composite material has the advantages that: the selected magnesium alloy and the selected zinc alloy have good biocompatibility and degradability; mechanical properties and a degradation rate of the integral composite material are controlled by controlling a relative thickness of a Zn layer to a Mg layer, so that the composite material adapts to a service environment, and therefore, a condition that single metal is too quick or too slow in degradation is solved. The material design and the preparation method are simple and convenient, and the cost is low, so that industrial production is facilitated.

The invention relates to a method for preparing Mg2Si/Mg composites by recovered silicon powder, which is characterized by including steps of drying a crucible required by experiment into a drying oven, adding magnesium alloy into a pit furnace for heating, injecting SF6+CO2 mixed protection gas and heating to the temperature ranging from 750 DEG C to 1100 DEG C for 1 to 3 hours until the magnesium alloy is melted; adding industrial dust silicon powder with 70% to 75% of silicon dioxide into water, adding the silicon powder, which is 2.5-7.5wt% of the magnesium alloy and wrapped by aluminum foil, into the magnesium alloy melt, ; mixing so that the magnesium alloy and the silicon powder can be reacted sufficiently; modifying, cooling naturally, then pouring the melt to a preheated metal mold with the preheating temperature ranging from 100 DEG C to 400 DEG C. During the integral mixing and casting process, protection gas must be injected continuously, and accordingly the Mg2Si/Mg composites are prepared. The industrial dust silicon powder is used as a silicon source and in-situ chemical reaction of the magnesium and the silicon powder is realized by means of mixing and casting. Themethod for preparing Mg2Si/Mg composites is simple in process and low in preparation cost, and the prepared Mg2Si/Mg composites are excellent in performances.

The invention relates to a method for preparing spinel whisker reinforced aluminum-based composite foam by in-situ synthesis. The method comprises the following steps of preparing Al-Mg powder according to the mass ratio of 7.4-16 to 1; dropping PVA (Polyvinyl Alcohol) solution with the mass fraction of 3 to 5 percent into the Al-Mg powder according to the mass-to-volume ratio of 13-14g to 1-2ml, grinding the mixture and drying the mixture under the air condition to obtain composite powder, then uniformly mixing the composite powder and NaCl particles according to the mass ratio of 0.29 to 1.16 and pressing the mixture at room temperature and the pressure of 300 to 400MPa into bulk materials; raising the temperature of the bulk materials to be 600 to 800DEG C at the temperature rise rate of 5 to 10DEG C/Min under the atmosphere of argon gases, sintering the bulk materials at the above temperature for 1 to 4 hours and then cooling the sintered materials along with the furnace to obtain an Al-Mg composite material bulk; cleaning the Al-Mg composite material bulk. The method disclosed by the invention has the advantages that the process of preparing foamed aluminium is simple and controllable, and the porosity is adjustable.

The invention discloses a preparation method for a shell-nacreous-layer-imitating magnesium-based composite material. A SiC particle reinforced magnesium-based composite material of a distinct shell-nacreous-layer structure can be prepared through the preparation method. A shell-nacreous-layer microstructure serves as a model, and a directional freeze thawing ice template method and a laminated hot pressing technique are adopted for preparing a biomimetic SiCp/Mg composite material with distinct shell-nacreous-layer microstructure characteristics and a controllable organizational structure. According to the novel preparation technique for biomimetic metal-based composite materials, the route is unique and the production efficiency is high. Compared with traditional magnesium-based composite materials, the prepared magnesium-based composite material of the shell-nacreous-layer-imitating structure not only has good mechanical properties such as high specific strength, high specific stiffness, good abrasion resistance, but also has good toughness and plasticity.

This invention relates to components and preparation method for a composite carrier catalyst for ethylene homopolymerization or copolymerization with other alpha-olefins. The catalyst comprises at least one Mg composite, at least one Ti compound, at least one organic alcohol compound, at least one Si compound, and at least one inorganic inert carrier. The Mg composite is prepared by dissolving Mg compound in organic epoxy compound and organic phosphorus compound system. The catalyst has such advantages as high catalytic activity, high hydrogen sensitivity and narrow particle size distribution of polymer. The catalyst is suitable for slurry polymerization of ethylene, combined polymerization process where catalyst with high activity and good particle morphology is needed, and gas phase fluidized bed process.

The invention provides a method for preparing an in-situ self-generated TiB2 reinforced composite material based on SLM. The method comprises the following steps of A1, taking KBF4 and K2TiF6 powdersas raw materials, and using a mixed salt reaction method for preparing the in-situ self-generated TiB2 nano-particle reinforced Al7SiCu 0.5Mg composite material; A2, carrying out vacuum atomization onthe composite material obtained in the step A1 to obtain a composite material powder; and A3, carrying out 3D printing on the composite material powder to obtain a SLM sample. According to the methodfor preparing the in-situ self-generated TiB2 reinforced composite material, the SLM is adopted to prepare the in-situ self-generated TiB2 nano-particle reinforced Al7SiCu 0.5Mg composite material, the microstructure of the composite material is greatly refined, and obvious holes or cracks are not observed in the composite material; and moreover, the strength is greatly improved on the premise that the plasticity is guaranteed, and huge application potential is obtained in the aerospace field.

The invention relates to composite magnetic nanoparticles Fe3O4/MPS/PAA/NTA-Ni<2+> and a preparation method and an application thereof in separation and purification of histidine-tagged proteins, and belongs to the technical fields of nano magnetic materials and biological analysis. Fe3O4 magnetic nanoparticles with an average hydration particle size of 100-400 nm are used as a core, MPS surface modification is adopted for making the surface rich in double bonds, polycarboxyl-structure magnetic nanoparticles with an average hydration particle size of 100-600 nm are obtained through PAA coating, and then furthermore, the polycarboxyl-structure magnetic nanoparticles are coupled with NTA-Ni<2+> to obtain the composite magnetic nanoparticles Fe3O4/MPS/PAA/NTA-Ni<2+> having fast magnetic field response. The prepared composite magnetic nanoparticles enable the thickness of a coating layer to be controlled in nanometer scale; the prepared composite magnetic nanoparticles have the advantages of uniform size distribution, strong magnetic and low cost, have higher ability of enrichment and separation purification of the histidine-tagged proteins, and have the purification efficiency of the histidine-tagged proteins as high as 40-70 [mu]g/mg composite magnetic nanoparticles; and the composite magnetic nanoparticles can be repeatedly used.

A stationary phase for ion-exchange chromatography is provided. The stationary phase comprises a chromatographic matrix superficially coated with hydroxyapatite. The stationary phase for ion-exchange chromatography has good biocompatibility and bioaffinity and higher mechanical strength. The stationary phase for ion-exchange chromatography is prepared by the following steps: activating an inorganic chromatographic matrix material such as silica gel or Zr/Mg composite oxide, immersing the matrix material into an oversaturated calcium/phosphorus solution, standing for deposition at 36.5 plus or minus 0.5 DEG C to obtain hydroxyapatite coating, washing with water twice, and drying to obtain the hydroxyapatite-coated stationary phase for ion-exchange chromatography in the protein separation. The method is also used to prepare a coating on the inner wall of a capillary tube to reduce the non-specific adsorption of proteins and simultaneously to provide an ion-exchange function for improvement of separation selectivity.

The present invention relates to two methods for preparing nanometre Ce-Mg composite oxide, which belongs to the superfine Ce-Mg composite oxide powder preparation field. Sol gel method has the reaction material of cerium nitrate hexahydrate and basic magnesium carbonate, and has a complexing agent of malic acid, wherein the cerous nitrate and the basic magnesium carbonate are dissolved in water respectively and then are mixed with each other, then malic acid is added therein before agitating at room temperature, and then ammonia liquor is dropped therein to adjust the pH value, so as to obtain nanometre Ce-Mg composite oxide after evaporating solvent, drying and calcining. The self-propagating combustion method has reaction substrate of cerium nitrate hexahydrate and magnesium nitrate, and has a complexing agent of malic acid, wherein the malic acid is dissolved in water, then cerous nitrate and magnesium nitrate are added therein synchronously before agitating at room temperature, and then ammonia liquor is dropped therein to adjust the pH value, so as to obtain nanometre Ce-Mg composite oxide after evaporating solvent, drying and calcining. The two methods can all obtain Ce-Mg composite oxide powder having a small particle diameter, a uniform dispersion and a large specific surface.

The invention discloses strengthened type nanometer WC/AlSi10Mg composite powder and an additive manufacturing technology and belongs to the technical field of additive manufacturing. The additive manufacturing technology comprises the following steps of adding 0.1 percent of nanometer WC in AlSi10Mg powder, performing mixing on the two powders for 20min with a GH-17 type three-dimensional motionefficient mixer, and then performing drying for 10h with a vacuum drying tank to obtain the strengthened type nanometer WC/AlSi10Mg composite powder. The composite powder has the characteristics of better mobility, high sphericity degree, high printing stability and the like; and by melting and solidifying the composite powder with laser, the plasticity of AlSi10Mg alloy is improved while the strength of the AlSi10Mg is improved.

The invention provides a preparation method for preparing an aluminum-based composite material based on laser selective melting. The preparation method comprises the following steps: S1, with KBF4 andK2TiF6 powders as raw materials, an in-situ self-generated TiB2/AlSi10Mg composite material is prepared by a mixed salt reaction method (LSM), and a composite material powder is prepared by vacuum gas atomization of the in-situ self-generated TiB2/AlSi10Mg composite material; S2, an SLM sample is prepared by laser selective melting of the composite material powder; and S3, the SLM sample is subjected to single aging treatment. The in-situ self-generated TiB2 particle reinforced AlSi10Mg composite material is prepared by the SLM, crystal grains are greatly refined, the mechanical properties ofthe material are further improved by the single aging treatment, and the composite material has great potential in the technical field of aviation and aerospace.

The invention discloses a preparation process of a biodegradable PCL (polycaprolactone)/Mg composite material FDM (fused deposition modeling) consumable. The preparation process comprises the following steps: mixing raw materials Mg and PCL for granulation through a parallel double-screw extruder, directly performing mixing, extrusion and granulation through a single-screw extruder or performing mixing and granulation with a solution method, thus obtaining the biodegradable PCL/Mg composite material FDM consumable. The Mg in the raw materials accounts for 5 to 50 percent of the mass of the PCL. The prepared biodegradable PCL/Mg composite material FDM consumable has the advantages that the degradation time in a human body is controllable, and the bone repair effect is better than that of pure PCL.

The invention provides a preparation method of a Ni-Co-Al-Mg composite hydroxide, wherein the method includes the steps of: performing a reaction to a raw material being a mixed salt solution of nickel, cobalt, aluminum and magnesium with urea as a precipitation and complexation agent in a hydrothermal reaction kettle at 100-180 DEG C for 12-48 h to prepare Ni-Co-Al-Mg composite hydroxide; and washing and drying the Ni-Co-Al-Mg composite hydroxide. By means of the method, aluminum ions can be uniformly co-precipitated with nickel, cobalt and magnesium ions within the same pH range, thus producing the a Ni-Co-Al-Mg precursor having stable ingredient and distribution and used for a lithium ion battery.

The invention discloses an Si-Mg composite insulation board and a production method thereof. The Si-Mg composite insulation board comprises a composite silicate insulation board, and the upper face and the lower face of the composite silicate insulation board are sequentially provided with a first magnesium oxychloride cement layer, a non-woven mesh fabric and a second magnesium oxychloride cement layer from inside to outside. The production method comprises the following steps of: sequentially coating first magnesium oxychloride cement slurry, adhering the non-woven mesh fabric and coating second magnesium oxychloride cement slurry on both sides of the composite silicate insulation board from inside to outside, and then naturally airing under normal temperature. In the invention, any adhesive is not used at the same time of enhancing the flexural strength of the composite silicate insulation board, therefore, the cost is reduced, and the problems of surface dregs and high requirements to the adhesives of the composite silicate insulation board are also solved; the production method is simple and easy to operate; and the production process is not restricted by the environment and is simple and convenient.

The invention discloses a laser additive manufacturing method of an in-situ synthesized nano Al2O3 reinforced aluminum-based composite material. The method comprises the following steps of (1) mixingZnO ceramic powders and AlSi10Mg aluminum alloy powders, and carrying out ball milling to obtain ZnO/AlSi10Mg composite powders; (2) carrying out additive manufacturing forming on the composite powders by adopting a selective laser melting process to form a solid sheet layer; (3) carrying out laser scanning on the solid sheet layer again to form a remelting sheet layer; (4) repeating the steps (2)and (3), and finally forming to obtain the in-situ synthesized nano Al2O3 reinforced aluminum-based composite material. A laser is used for exciting Al and ZnO to generate aluminothermic reactions between the Al and ZnO to generate Al2O3 ceramic particles in situ, the overall process design of the method is improved, selective laser melting and laser remelting scanning are matched, the prepared aluminum-based composite material is high in density and fine in microstructure, the in-situ synthesized Al2O3 particles are nanoscale in size and are uniformly distributed, and the phase interfaces ofthe Al2O3 particles are well combined with an aluminum matrix.

The invention provides a styrene-acrylonitrile- diene copolymer compound includes 5 to 40 parts by weight of copolymer mixture (A); 5 to 30 parts by weight of halogen fire retardant (B); 1 to 10 parts by weight of antimonial oxide (C); 0.2 to 2.5 parts by weight of di-methyltin mercaptide maleate polymer (D); 0.2 to 1.5 parts by weight of al-mg composite metal salt (E); and 60 to 95 parts by weight of vinyl benzene- acrylonitrile copolymer (F). The copolymer mixture (A) is formed by mixing first copolymer component (A1), second copolymer component (A2) and third copolymer component (A3). The vinyl benzene- acrylonitrile copolymer has good thermo-stability, low-temperature impact strength and flame retardancy.

The invention discloses a high-interface-strength Cf/Mg composite material and a preparation method thereof, belongs to the field of light structural materials and particularly relates to a high-interface-strength Cf/Mg composite material and a preparation method thereof. The high-interface-strength Cf/Mg composite material disclosed by the invention is used for solving the problem that an existing Cf/Mg composite material is low in interface bonding strength. The high-interface-strength Cf/Mg composite material is prepared from carbon fibers and magnesium-yttrium alloy, wherein the magnesium-yttrium alloy is prepared from pure yttrium alloy and pure magnesium. The preparation method comprises the following steps: (1) preparing a carbon fiber reinforcement prefabricated member by using a fiber winding machine; (2) smelting pure magnesium and pure yttrium to obtain a magnesium-yttrium alloy melt solution; (3) pressing the carbon fiber reinforcement prefabricated member into a cavity of a forming mold, then filling the magnesium-yttrium alloy melt solution into the forming mold and then pressing to obtain a fiber reinforced magnesium-based composite material; and (4) cooling the fiber reinforced magnesium-based composite material to room temperature along with the mold, demolding and then mechanically removing excess magnesium-yttrium alloy from the edge to obtain the Cf/Mg composite material.

The invention discloses a liquid-solid pressure formation device and method for thin-wall special-shaped parts made of Cf-Mg composite materials. The liquid-solid pressure formation device and method for the thin-wall special-shaped parts made of the Cf-Mg composite materials are used for solving the technical problem that prefabricated parts with complex inner wall structures are difficult to form by an existing fiber-reinforced intermetallic compound composite part manufacturing device. According to the technical scheme, a split insert structure replaces an integrated mandrel to shape the prefabricated parts. Compared with the integrated mandrel, the inner side of an insert set is hollow, a male mould is small, and the overall weight of a formation device can be reduced; magnesium alloy fluid is prompted to permeate the prefabricated parts evenly through the radial movement generated by stress on inserts; the surfaces of the inserts are tightly attached to the inner walls of the prefabricated parts, and the sizing effect is remarkable; near-net forming of the different-shape thin-wall special-shaped parts made of the Cf-Mg composite materials can be achieved by changing the shapes of sections of the inserts; the inserts are separated after extrusion is completed to achieve demoulding, and the technical problems that the prefabricated parts with the complex inner wall structures are high in sizing difficulty, and demoulding is difficult are effectively solved, and forming of the thin-wall special-shaped parts made of the Cf-Mg composite materials is achieved.

The invention discloses a method for preparing a 2-chloro-3,3,3-trifluoropropylene catalyst by gas phase fluorination. The method comprises the following steps of preparing a mixed solution from a ferric soluble salt and a magnesium soluble salt according to a certain mole ratio of Fe/Mg, adding a precipitating agent into the mixed solution, carrying out aging, drying and roasting for a certain time to obtain a Fe-Mg composite oxide, blending the Fe-Mg composite oxide and magnesium carbonate according to a certain mass ratio, carrying out grinding and pressing molding to obtain a catalyst precursor, carrying out roasting and carrying out HF gas fluorination to obtain the fluorination catalyst. The 2-chloro-3,3,3-trifluoropropylene catalyst prepared by gas phase fluorination has a service life more than 1200h, has strong stability, can be regenerated after catalyst performance reduction so that catalyst performances are recovered and can be recycled.

The invention discloses a 2,4-dichlorphenoxyacetic acid preparation method which comprises the following special steps: adding chloroacetic acid into a sodium hydroxide solution, stirring, adding into phenol, and regulating the PH value to 11 with sodium bicarbonate; then heating for 40 minutes at 100 DEG C; adding into hydrochloric acid to regulate the PH value to 4; finally cooling in an ice-water bath, and washing and drying the obtained solid to obtain phenoxyacetic acid; adding into the phenoxyacetic acid into an acetic acid and water mixed solution, adding into an Ni-Al-Mg composite oxide, stirring and mixing, wherein the mass of the Ni-Al-Mg composite oxide is 0.05% of that of phenoxyacetic acid; then introducing chlorine to carry out chlorination; reacting for 20-40 minutes, and finishing the chlorination; then cooling the reaction product, and filtering to obtain a solid; at last, drying the solid to obtain the 2,4-dichlorphenoxyacetic acid. The product prepared by the method disclosed by the invention is high in quality, yield and purity; the preparation process is simple, convenient and stable, the industrial cost is low, and the environment is protected.