2301 results about "Magnesium" patented technology

The invention provides an acetylacetone-based composite thermal stabilizer which is a mixture obtained by mixing zinc acetylacetonate, calcium acetylacetonate or magnesium acetylacetonate and hydrotalcite pro rata. The composite thermal stabilizer is suitable for chloride-containing high polymer, such as polyvinyl chloride, chlorinated polyethylene, chlorinated polyvinyl chloride, copolymer of vinyl chloride-ethylene or copolymer of vinyl chloride-vinyl acetate, has better thermal stability, prolongs the thermal aging time of the chloride-containing high polymer, and overcomes the shortcomings of poor long-term performance of single stabilizer of zinc acetylacetonate, poor transparency of stabilizer of calcium acetylacetonate, and poor initial colorability of stabilizer of hydrotalcite. The composite thermal stabilizer has low cost, good initial colorability, excellent long-term performance and good transparency, and is an efficient composite thermal stabilizer.

The invention relates to a zirconia-based all-ceramic false tooth and a preparation method thereof. A core layer of the zirconia-based all-ceramic false tooth is prepared from the following components in parts by mass: 90 to 94 parts of ZrO2, 5 to 9 parts of Y2O3, 0.1 to 0.5 part of Al2O3, 0.01 to 0.5 part of Fe2O3, 0.01 to 0.5 part of Er2O3 and 0 to 0.2 part of MnO2, and a shell layer of the zirconia-based all-ceramic false tooth is prepared from the following components in parts by mass: 24.5 to 49.5 parts of CaCO3, 45 to 50 parts of SiO2, 0 to 25 parts of MgO, 0.01 to 0.5 part of Fe2O3, 0.01 to 0.5 part of Er2O3 and 0 to 0.2 part of MnO2. The preparation process comprises the following steps: performing dry pressing and isostatic pressing on raw materials of the core layer, presintering, and carving to obtain a zirconia-based false tooth biscuit; meanwhile, calcining raw materials of a shell layer, then adding deionized water, a dispersing agent and an adhesive, and carrying out ball milling and mixing to obtain calcium-magnesium-silicon-based ceramic slurry; and coating the calcium-magnesium-silicon-based ceramic slurry on the surface of the zirconium oxide-based false tooth biscuit, and sintering to obtain the zirconium oxide-based all-ceramic false tooth provided by the invention. The zirconia-based all-ceramic false tooth has good jade texture and is closer to the natural color of natural teeth.

The invention discloses a fluoride salt-free nitrate-free cast iron enamel semitransparent glaze as well as a preparation method and application thereof, and belongs to the technical field of enamel. The semitransparent glaze is prepared from quartz, anhydrous borax, sodium carbonate, potassium carbonate, calcium carbonate, potassium feldspar, zinc oxide, lithium carbonate, zirconium silicate, titanium dioxide, aluminum oxide, trisodium phosphate, antimony oxide, magnesium carbonate and barium carbonate according to a specific mass ratio. The preparation method comprises the steps of raw material mixing, high-temperature melting under a pure oxygen condition, wiredrawing detection, quenching and the like. The semitransparent glaze is completely free of fluoride salt and nitrate, the problems of fluoride emission and environmental protection equipment blockage are avoided from the source, the fluorine content of the product is not detected through detection, the product meets the requirements of European Union REACH regulations, meanwhile, the product has good porcelain surface, luster and low-temperature firing adaptability, and is suitable for cast iron matrixes, the firing temperature is 740-760 DEG C, and the firing time is 2-3 hours. The method can be used for producing green and environment-friendly enamel products.

The invention discloses multi-source composite expansion super-early-strength concrete and a preparation method thereof. The concrete comprises a cementing material, aggregate, a water reducing agent, water and a multi-source composite expansion system. The expansion system is composed of a plastic expansion agent, a calcium sulphoaluminate early expansion source, a magnesium oxide delayed expansion source and an internal curing material. Through precise component design and function time sequence matching, a cooperative compensation network covering the whole life cycle of the concrete is constructed, a plastic expanding agent inhibits plastic shrinkage, calcium sulphoaluminate compensates early-stage self-shrinkage, magnesium oxide resists medium-and-long-term drying shrinkage, an internal curing material provides continuous moisture guarantee for the above process, and the overall performance of the concrete is improved. And the efficiency of each expansion source is excited and coupled. According to the invention, seamless and accurate shrinkage compensation from a plastic stage to a service later stage can be realized on the premise of ensuring the super early strength characteristic of the concrete, the technical problem that the super early strength concrete is easy to crack due to severe shrinkage is fundamentally solved, and the volume stability and durability of the structure are remarkably improved.

The invention provides titanium-containing anhydrous stemming for a blast furnace and a preparation method of the titanium-containing anhydrous stemming, and belongs to the technical field of refractory materials for the blast furnace. The titanium-containing anhydrous stemming for the blast furnace comprises the following raw materials: 40-60 parts of titanium corundum, 5-15 parts of silicon carbide, 10-20 parts of ferro-silicon nitride fine powder, 5-15 parts of titanium dioxide fine powder, 5-15 parts of vanadium-titanium slag fine powder, 5-10 parts of coke fine powder, 1-5 parts of monatomic silicon fine powder, 1-5 parts of ball clay micro powder, 1-5 parts of aluminum nitrate micro powder and 1-2 parts of magnesium alon micro powder. Gas-phase substances of Si (g), Al (g) and Mg (g) can be formed in the stemming at high temperature by the monatomic silicon fine powder and the MgAlON micro powder in the raw materials and react with CO and N2 in the environment to generate ceramic whiskers such as SiC, Si3N4, AlN and MgAl2O4, and the generated ceramic whiskers are distributed in a staggered manner and are filled in pores of the stemming, so that the high-temperature strength and the volume stability of the stemming are remarkably improved.

The invention relates to an automatic magnesium oxide coating analysis system and method, and belongs to the technical field of coating quality analysis. The method comprises the following steps: acquiring attributes of a magnesium oxide coating, an infrared spectrum and environment temperature and humidity data, and constructing a multi-source feature set; analyzing the distribution dispersion and local enrichment risk of free water based on a dynamic migration model, and analyzing the bonding weakening degree and dissociation risk of bound water based on a chemical stable state model; respectively generating free water treatment process parameters for inhibiting structural damage and combined water treatment process parameters for preventing performance degradation according to the abnormal analysis result and the coating attribute; by performing coupling influence analysis on the two types of process parameters, the balance requirements of the structural integrity and chemical stability of the coating are coordinated, an optimized process scheme is generated, and cooperative regulation is realized. According to the method, accurate identification, independent analysis and cooperative control of the free water and the bound water are realized, and the accuracy, reliability and quality consistency of coating water treatment are improved.

The invention discloses a controllable preparation method for the eutectic phase size of a medium-aluminum type zinc-aluminum-magnesium coating, which comprises the following steps of: preparing the following components in percentage by weight: 0.01 to 0.08 percent of C, less than or equal to 0.03 percent of Si, 0.15 to 0.26 percent of Mn, 0.15 to 0.26 percent of P, less than or equal to 0.01 percent of S, 0.02 to 0.06 percent of Als, less than or equal to 0.3 percent of Ti and the balance of Al; the base material is subjected to annealing treatment, zinc plating treatment and post-plating treatment after multiple working procedures, and the plating layer with the ternary eutectic structure morphology is obtained. Through optimization of base material components, the galvanizing process and the cooling process, accurate control over the eutectic phase size in the plating layer is achieved, and therefore the corrosion resistance, the adhesive force and the uniformity of the plating layer are improved.

The invention provides an optimization method of a magnesium slag sensible heat recovery system, which comprises the following steps: acquiring particle size distribution data of magnesium slag particles, and judging whether the problem of non-uniform particle size distribution exists or not according to a preset particle size threshold value; aiming at the problem of non-uniform particle size distribution, magnesium slag particles are classified by adopting a clustering algorithm, and the distribution areas of large particles and small particles are determined; according to the distribution area of the large particles, the rotating speed of the cooling roller is dynamically adjusted, and the accumulation probability of the large particles in the roller is reduced; the temperature change trend of the inner wall of the cooling roller is monitored in real time, and if it is detected that the local temperature abnormally rises, it is judged that local hot spots exist; when a local hot spot is detected, a spraying cooling system in the roller is started, and intensified cooling is conducted on a local area; pressure and temperature data of high-pressure and high-temperature water are collected in real time through a pressure sensor and a temperature sensor, and whether fluctuation exists or not is judged.

The invention discloses a fluoride-salt-free and nitrate-free cast iron enamel zirconium white glaze as well as a preparation method and application thereof, and belongs to the technical field of enamel. The zirconium white glaze is prepared from quartz, borax pentahydrate, magnesium carbonate, potassium carbonate, potassium feldspar, zinc oxide, aluminum hydroxide, calcium carbonate, zirconium silicate, sodium tripolyphosphate and lithium carbonate according to a specific mass ratio. The preparation method comprises the steps of raw material mixing, high-temperature melting under a pure oxygen condition, wiredrawing detection, quenching and the like. The zirconium white glaze is completely free of fluoride salt and nitrate, the problems of fluoride emission and environmental protection equipment blockage are avoided from the source, the fluorine content of the product is not detected through detection, the product meets the requirements of European Union REACH regulations, and meanwhile, the zirconium white glaze has good porcelain surface, luster and firing adaptability, is suitable for cast iron matrixes, has the firing temperature of 740-760 DEG C and the firing time of 87-87 hours, and can be widely applied to cast iron substrates. The method can be used for producing green and environment-friendly enamel products.

The invention discloses a super-early-strength shrinkage-free high-crack-resistance tunnel spraying repair material in the technical field of civil engineering materials, which comprises the following raw materials in percentage by mass: 35-45% of sulphoaluminate cement; 8%-12% of a superfine early strength admixture; 2%-3% of a calcium sulphoaluminate expanding agent; 1%-2% of a magnesium oxide-based expanding agent; 1-2% of a calcium-magnesium composite expanding agent; 10%-15% of hollow glass beads; 1.5%-2.5% of copper plated steel fiber; 0.1%-0.3% of polypropylene fiber; 25%-30% of graded quartz sand; 0.5%-1.0% of a polycarboxylic acid water reducing agent; 3%-5% of an alkali-free liquid accelerator; 0.3%-0.8% of a thixotropic agent; and 0.1%-0.3% of a thickening time control agent. According to the method, a multi-scale performance cooperative regulation system is innovatively constructed. Through accurate control of the hydration process of a gel system, a shrinkage stress multi-stage compensation mechanism and systematic integration of a fiber-matrix interface strengthening technology, the mutual restriction relationship among early strength development, volume stability and crack resistance of a traditional material is broken through.

The invention relates to the technical field of grouting materials, in particular to a dynamic water environment anti-dispersion micro-expansion grouting material and a preparation method thereof. A component A of the grouting material mainly comprises the following raw materials in parts by weight: 120-160 parts of a gel material with volcanic ash characteristics, 3-5 parts of a retarder, 10-15 parts of magnesium oxide, 0.5-2 parts of citric acid, 5-8 parts of aluminum sulfate, 1-2 parts of sodium fluoride, 0.5-1 part of gelatin and 70-100 parts of water; the component B mainly comprises the following raw materials in parts by weight: 4-8 parts of polyacrylamide, 5-10 parts of polyacrylic acid derivative salt, 1-2 parts of alcohol polysaccharide, 40-100 parts of water glass and 30-50 parts of water; magnesium oxide, aluminum sulfate, gelatin and sodium fluoride in the component A are prepared into core-shell anti-dispersion particles in advance; the problems that a traditional cement grouting material is poor in anti-scouring capacity and anti-dispersing capacity, low in retention rate, poor in stone durability and the like can be solved.

The invention discloses fluoride-salt-free and nitrate-free low-temperature pearlescent glaze for steel plate enamel as well as a preparation method and application of the pearlescent glaze, and belongs to the technical field of enamel. The pearlescent glaze is prepared from quartz, anhydrous borax, titanium dioxide, magnesium carbonate, sodium tripolyphosphate, potassium carbonate, lithium carbonate, potassium feldspar, zinc oxide and V-26 according to a specific mass ratio. The preparation method comprises the steps of raw material mixing, high-temperature melting under a pure oxygen condition, wiredrawing detection, quenching and the like. The pearlescent glaze is completely free of fluoride salt and nitrate, the problems of fluoride emission and environmental protection equipment blockage are avoided from the source, the fluorine content of the product is not detected through detection, the product meets the requirements of European Union REACH regulations, meanwhile, the pearlescent glaze has good porcelain surface, luster and low-temperature firing adaptability, is suitable for a steel plate matrix, has the firing temperature of 760-800 DEG C and the firing time of 10-20 minutes, and is suitable for a steel plate. The method can be used for producing green and environment-friendly enamel products.

The invention relates to the field of test and analysis of impurity element content of primary magnesium ingots, in particular to a method for testing impurity element content of primary magnesium ingots by ICP (inductively coupled plasma) spectrometry, which comprises the following steps: firstly adding H2O2 into a magnesium ingot sample to infiltrate the sample, then adding HCl at an interval of less than 1 minute to carry out first reaction, carrying out first heating after the reaction is finished, and then carrying out second heating, cooling to 20-30 DEG C, transferring to a volumetric flask, and fixing the volume by using third-level water to obtain a sample solution; establishing a working curve by using an ICP spectrometer and a standard solution; testing the sample solution; the ratio of the mass of the magnesium ingot sample to the volume of H2O2 to the volume of HCl is 1: (3-10): (30-54), the method fills the standard vacancy of ICP spectrometry analysis of the silicon element in the primary magnesium ingot, a reliable basis is provided for chemical component analysis of the primary magnesium ingot, the test result is surface, and the method for testing the mass fraction of the impurity elements in the primary magnesium ingot provided by the invention has the advantages of high analysis precision, simple operation, high accuracy and high reliability. The analysis period is short, and related chemical varieties are few.

The invention relates to the technical field of mineral processing, and particularly provides a combined reagent system for flotation and magnesium reduction of talc-containing copper-molybdenum ore and application of the combined reagent system. The combined reagent system comprises a flotation collecting agent (faint yellow to orange transparent liquid, 40%-50% of active ingredients and less than or equal to 3% of free alkali) with active ingredients in the formula 1 and a flotation depressing agent (light yellow powder, extracellular polysaccharide extract of xanthomonas, the weight-average molecular weight of 1000-1500000 Daltons and rich in hydroxyl, carboxyl and pyruvic acid groups) with a structural formula in the formula 2, and the flotation depressing agent comprises extracellular polysaccharide extract of xanthomonas, the weight-average molecular weight of xanthomonas and the weight-average molecular weight of xanthomonas and is rich in hydroxyl, carboxyl and pyruvic acid groups. Through the synergistic adsorption effect of the combined reagent, the flotation grade and the recovery rate of the copper sulfide molybdenum ore are remarkably improved under the condition that the pH is 8-11. The combined reagent system has the advantages of being high in flotation efficiency, high in selectivity, low in reagent cost, environmentally friendly, high in industrial applicability and the like.

A beneficiation method for improving a grade of a magnesium-containing copper sulfide ore concentrate includes: crushing and grinding an ore to a fineness degree allowing 55% to 65% of particles to pass through a 0.074 mm sieve, adding an adjusting agent lime, collecting agents butylxanthate and kerosene, and a foaming agent methyl isobutyl carbinol (MIBC) to obtain a copper-molybdenum-sulfur mixed concentrate; re-grinding the copper-molybdenum-sulfur mixed concentrate to a fineness degree allowing 75% to 82% of particles to pass through a 0.048 mm sieve, adding lime, a magnesium-containing silicate inhibitor, a collecting agent 1, and MIBC to obtain a copper-molybdenum mixed concentrate; and adding sodium sulfide, kerosene, and MIBC to the copper-molybdenum mixed concentrate to obtain a high-grade copper concentrate. The beneficiation method adopts mixed flotation of copper-molybdenum, regrinding for separating copper and molybdenum from sulfur, and magnesium removal from a copper concentrate to allow quality improvement for the copper concentrate.

The invention belongs to the technical field of fertilizers, and particularly relates to magnesium-containing controlled-release urea and a preparation method thereof, and the magnesium-containing controlled-release urea is characterized in that magnesium or magnesium-boron, magnesium-zinc and magnesium-boron-zinc medium trace element combinations are added into large-particle urea, and then coating is carried out. According to the controlled-release urea, elements such as magnesium are added into molten urine, then roller granulation and cooling are carried out, and finally coating is carried out. According to the prepared product, urea, magnesium and other elements can be synchronously and slowly released for a long time, nitrogen, magnesium and other nutrients have synergistic benefits, the utilization rate of nitrogen fertilizer, magnesium and other elements can be further increased, robust growth of crops is promoted, the yield is increased, the quality is improved, the stress resistance is enhanced, and labor is saved; and the method is especially suitable for regions with relatively common lack of medium trace elements and high-added-value commercial crops, and has a wide practical application value.

A steel sheet, coated with a metallic coating including, by weight percent, from 7.5 to 9.0% of zinc, from 1.1 to 4.0% of silicon, from 1.1 to 8.0% of magnesium, up to 3.0% of iron, optional elements chosen from Pb, Ni, Zr, or Hf, the content by weight of each element being less than 0.3%, optionally up to 100 ppm of Calcium and unavoidable impurities up to 0.02%, a balance being aluminum, and wherein the coating weight of the metallic coating is from 50 to 500 g / m2 for the sum of both sides of the-steel sheet.

The present disclosure relates to the technical field of solid-state hydrogen storage materials, and specifically provides a magnesium-based hydrogen storage material based on a core-shell structure, a preparation method therefor, and use thereof. The magnesium-based hydrogen storage material based on a core-shell structure provided by the present disclosure comprises a hydrogenated combustion product of Ni / Fe3O4@MIL and MgH2, wherein Ni / Fe3O4@MIL is a material having a core-shell structure. An inner core of Ni / Fe3O4@MIL comprises Ni-loaded Fe3O4 microspheres, and an outer shell of Ni / Fe3O4@MIL comprises an organic ligand. The magnesium-based hydrogen storage material based on a core-shell structure significantly improves the hydrogen storage performance of magnesium hydride, and can still maintain a high hydrogen absorption capacity at a low temperature.

The invention relates to preparation of a ZTA composite ceramic material, and belongs to the field of inorganic nonmetal composite materials. The raw material composition formula comprises aluminum oxide, zirconium oxide, zirconium dioxide, yttrium oxide, magnesium oxide and titanium dioxide. The low-sodium microcrystalline alumina powder with the original grain size of 0.40 [mu] m is selected and ground to the original grain size in advance, so that zirconia can be more uniformly distributed between alumina grain boundaries, which is a precondition for obtaining more uniform ZTA. Zirconium dioxide is creatively introduced, and compared with a conventional method in which stable zirconium oxide is directly used, the cost of ZTA is greatly reduced. The pre-calcined granulation powder is adopted, so that a ZTA product which is uniformly mixed in the early stage is cured by adding a stabilizer, and then the uniform and stable ZTA ceramic can be obtained through later-stage forming and firing.

The utility model relates to a hydrogen purification system based on magnesium-based hydride, which comprises a buffer tank, a gas inlet of the buffer tank is connected with a discharge end of a hydrogen purification module through a first gas path header pipe, and a vacuum pump is mounted on the first gas path header pipe in a matched manner. An exhaust port of the buffer tank is connected with a feeding end of the hydrogen purification module through a second gas path header pipe, a metal hydrogen storage material is arranged in the hydrogen purification module, and a feeding port of the buffer tank is connected with an exhaust port of the feed gas storage device through a third gas path header pipe. By arranging the hydrogen purification module, hydrogen components in raw material gas can be absorbed based on magnesium hydride, and compared with some traditional physical and chemical purification schemes, the production cost is low; meanwhile, the number of hydrogen storage tanks in the hydrogen purification module can be reasonably set according to purification requirements, the use flexibility is good, the purity of obtained hydrogen is high, no other impurity gas is mixed in the purification process, and the working efficiency of the system is high.

The invention relates to the technical field of refractory materials, and provides a composite regenerated magnesia carbon brick and a preparation method thereof. The composite regenerated magnesia carbon brick is prepared from the following raw material components in parts by mass: 55 to 65 parts of waste magnesia carbon brick, 40 to 50 parts of fused magnesia, 7 to 10 parts of composite graphite, 3 to 5 parts of antioxidant and 4 to 7 parts of phenolic resin, the composite graphite is of a core-shell structure, and a core in the core-shell structure is magnesium oxide coated graphite; and the shell in the core-shell structure is 1, 3, 5-trimethoxybenzene. According to the technical scheme, the problem that the mechanical property of the composite regenerated magnesia carbon brick is poorer due to poorer wettability of phenolic resin on graphite in related technologies is solved.

The invention discloses a magnesium oxide supported catalyst, a preparation method and application in VOCs (volatile organic compounds) purification, and belongs to the field of volatile organic compound catalytic purification. Magnesium oxide is used as a carrier of the catalyst, and two modified materials are supported, one is a double-active-center material anchoring nickel single atoms and ruthenium clusters in a porous carbon-nitrogen framework, and the other is a double-active-center material anchoring nickel single atoms and ruthenium clusters in a porous carbon-nitrogen framework; and the other one is a defective carbonitride MXene intercalated hydroxyapatite nanosheet, and lanthanum oxide can be added as a cocatalyst. The preparation method comprises the following steps: sequentially loading the two modified materials on the magnesium oxide carrier, and carrying out ultrasonic dispersion, stirring, centrifuging, drying, calcining and the like, so that the active component and the carrier form strong interaction. According to the catalyst, through the synergistic effect of double active centers and the structural advantages of the modified material, the catalytic oxidation efficiency and stability of VOCs are remarkably improved, and the catalyst is suitable for purification treatment of industrial waste gas and volatile organic compounds in indoor air.

The invention provides a magnesium aluminate spinel-CMA multiphase material and a preparation method thereof, and belongs to the field of refractory materials. The refractory material comprises the following raw materials in percentage by mass: 80-87% of Al2O3, 6-19% of high-calcium magnesia and 1-7% of CaO. The mass percentage of the binding agent is 1-6% of the sum of the raw materials. The magnesium aluminate spinel-CMA multiphase material with excellent performance is synthesized from low-grade high-calcium magnesia, CMA large grains are tightly wrapped by magnesium aluminate spinel small grains, and a CMA phase and a magnesium aluminate spinel phase are uniformly distributed, so that the magnesium aluminate spinel-CMA multiphase material has the advantages of magnesium aluminate spinel and CMA materials, namely the magnesium aluminate spinel-CMA multiphase material has the characteristics of high hardness, wear resistance, thermal shock resistance, erosion resistance and the like.

This invention discloses a high-early-strength, low-shrinkage composite silicate cement and its preparation method, comprising: low-shrinkage silicate cement clinker, early-strength component, and gypsum component; the low-shrinkage silicate cement clinker is prepared from calcareous raw materials, siliceous-aluminous raw materials, ferrous raw materials, a first activator, and a mineralizer; its mineral composition includes: C3S 30-50 parts, C2S 20-40 parts, C3A 0.5-5 parts, and C4AF 10-25 parts; its particle size distribution characteristics are D10≥5μm, D90≤45μm, uniformity index of 1.2-1.6, and characteristic particle size of 25-30μm; the early-strength component is prepared from F-type fly ash or C-type fly ash, limestone, magnesium oxide, and a second activator; its mineral composition includes: C 20 A 13 M3S 350-65 parts, C2S 35-50 parts. The cement prepared by this invention not only has high early strength, but also has a small drying shrinkage rate.

A new method for extracting lithium from salt lake brine, comprising the following steps: a salt lake old brine raw material, desorption liquid, low-magnesium water, and adsorption tail liquid pass through an old brine feeding pipe (2), a desorption liquid feeding pipe (4), a low-magnesium water top desorption liquid feeding pipe (3), and an adsorption tail liquid top desorption liquid feeding pipe (11), respectively, which are located above and below a rotary disc of a multi-way valve system (1); and after respectively entering corresponding adsorption columns (6) by means of a duct and channel within the multi-way valve system (1), the entire process procedure is completed from an adsorption tail liquid discharge pipe (7), a qualified desorption liquid discharge pipe (10), a lithium-containing old brine discharge pipe (8), and an adsorption tail liquid top desorption liquid discharge pipe (5); and the adsorption columns (6) are connected in series or in parallel by means of channels located in the multi-way valve system (1). The feature in which a multi-way valve device is simple and easy to operate is utilized, and in comparison with a fixed bed operating system, the utilization rate of lithium adsorbent may be increased by over 20%, the utilization efficiency of the lithium adsorbent may be increased by over 40%, and production costs may be reduced by 30-50%. Therefore, the stability of a qualified desorption liquid is improved, stable production is guaranteed, and year-round constant operation may be achieved.

The present invention relates to a vertical-retort reduction furnace for producing metal magnesium, comprising: a furnace body defining a furnace chamber (2), and vertical retorts (6) arranged in the furnace chamber (2), wherein the vertical retorts (6) each comprise a hollow straight cylindrical retort body (6-3); the retort body (6-3) defines, in an upper portion, a first crystallizer chamber (6-7) for receiving a crystallizer (7), and defines a second chamber (6-8) located below the first crystallizer chamber (6-7); the vertical retorts (6) each are provided with a top opening (6-10) and a bottom opening (6-6); the diameter of the bottom opening (6-6) is equal to the diameter of the second chamber (6-8). The vertical-retort reduction furnace further comprises bin assemblies (10), wherein the bin assemblies (10) each comprise an upper bin (10-1) allowing for filling of a pellet material (8) and a lower bin (10-4) for slidably receiving the upper bin (10-1). The present invention also relates to a method for producing metal magnesium by using the vertical-retort reduction furnace.

The invention discloses magnesium modified fecal sludge hydrothermal carbon as well as a preparation method and application thereof, and belongs to the technical field of solid waste treatment in the environmental protection industry. The invention relates to a preparation method of magnesium modified fecal sludge hydrothermal carbon. The preparation method comprises the following steps: uniformly mixing fecal sludge powder and a magnesium additive to obtain a mixture; taking water as a solvent, and adding the mixture for hydrothermal reaction to obtain the magnesium modified fecal sludge hydrothermal carbon. According to the invention, waste utilization is carried out on the excrement sludge, modification is carried out through the magnesium additive, and loss of nutrient substances such as nitrogen, phosphorus and the like is effectively reduced. The magnesium modified fecal sludge hydrothermal carbon is applied to soil, can effectively promote the growth of pakchoi, and has certain agricultural value.

A Zn—Al—Mg-based hot-dip plated steel sheet includes a hot-dip plated layer formed on a surface of a steel sheet, in which the hot-dip plated layer contains, as an average composition, Al: 5 to 22 mass % and Mg: 1.0 to 10 mass %, with a remainder including Zn and impurities, and in a case where a 5 mm square cross section parallel to a surface of the hot-dip plated layer is exposed at any position of a 3t / 4 position, a t / 2 position, and a t / 4 position from the surface with a thickness of the hot-dip plated layer represented by t, a ratio (B / A (%)) of an area fraction B of a [Zn phase] to a total area fraction A of a [Zn phase] and an [Al / MgZn2 / Zn ternary eutectic structure] of a plating microstructure in at least one cross section is 20% or more.

Magnesium oxide is provided. When magnesium oxide is dispersed in water at a ratio of 16 g of magnesium oxide per 100 g of water, the relaxation time of TD-NMR at 40°C satisfies the requirement of 1000 milliseconds or less.

The invention relates to the technical field of batteries, in particular to a core-shell material, a preparation method thereof and a negative electrode material. The preparation method of the core-shell material comprises the following steps: providing metal raw materials including magnesium, copper, aluminum, zirconium and lithium, and pretreating the metal raw materials into quinary alloy powder; the preparation method comprises the following steps: putting quinary alloy powder in an inert gas atmosphere or a micro-aerobic atmosphere, sequentially carrying out heating treatment and constant-temperature annealing treatment on the quinary alloy powder, forming a core layer Al3Zr and a shell layer Al3Li in the core-shell material in the heating treatment stage, and after the core layer and the shell layer are formed, mutually diffusing zirconium atoms and lithium atoms at the interface of the core layer and the shell layer to form a transition layer Al3 (Zr, Li), and at the constant-temperature annealing treatment stage, magnesium and copper form an Mg2Cu3 phase which is directly bonded with the surface of the shell layer, and copper atoms are directly bonded with the surface of the shell layer, so that the Al3Zr-coated Al3Li core-shell material is formed. A preparation method of the core-shell material with both mechanical strengthening and volume buffering is found.