8948 results about "Carbonization" patented technology

The invention relates to a method for preparing a carbon material with rich mesopores and macropores. Inorganic nano-particles are used as pore-forming template agent to be uniformly distributed in a carbon-contained organic precursor and then the carbon-contained organic precursor carries out high-temperature carbonization, template agent washing-out and drying to obtain a porous carbon material. The carbon material prepared by the method has the specific surface area of 50-1,900 m/g and a pore diameter mainly between 2-900 nm, can be conveniently adjusted by the size control of the selected nano-particles, removes a template without using high corrosive HF and has the advantages of simple method, convenient operation, free pore diameter adjustment and control in a mesopore and macropore range, and the like. The carbon material has a wide application prospect in fields of electrochemical energy accumulation, macromolecular adsorption, catalyst carriers, composite materials, and the like.

A process for preparing a patterned layer of aligned carbon nanotubes on a substrate including: applying a pattern of polymeric material to the surface of a substrate capable of supporting nanotube growth using a soft-lithographic technique; subjecting said polymeric material to carbonization to form a patterned layer of carbonized polymer on the surface of the substrate; synthesising a layer of aligned carbon nanotubes on regions of said substrate to which carbonized polymer is not attached to provide a patterned layer of aligned carbon nanotubes on said substrate.

The present invention relates to methods for producing carbon-based molded bodies. In particular, the present invention relates to methods for producing porous carbon-based molded bodies by carbonizing organic polymer materials mixed with non-polymeric fillers and subsequently dissolving the fillers out from the carbonized molded bodies. The present invention further relates to methods for producing porous carbon-based molded bodies by carbonizing organic polymer materials mixed with non-polymeric fillers which are substantially completely decomposed during the carbonization. The present invention also relates to a method for producing porous carbon-based molded bodies by carbonizing organic polymer materials, the carbon-based molded bodies being partially oxidized following carbonization so as to produce pores. In addition, the present invention relates to porous molded bodies produced according to one of said methods and the use thereof, especially as cell culture carriers and/or culture systems.

The invention relates to a method for preparing a C/SiC composite material through a low-cost fused silicon impregnation method, which comprises the following steps: performing calcining pretreatment on a carbon felt or graphite felt at 400-600 temperature; immersing the pretreated carbon felt or graphite felt in a melamine and boric acid solution, thus coating a boron nitride protective layer; immersing in a carbon/silicon carbide slurry water solution, performing impregnation to ensure that pores of the carbon felt or graphite felt are fully filled with carbon/silicon carbide, placing in a sintering furnace, and performing primary fused silicon impregnation treatment at 1600-1800 DEG C; immersing in liquid phenolic resin, and performing carbonization treatment under the protection of an inert atmosphere at 800-1000 DEG C to ensure that all the resin is carbonized; and finally, performing secondary fused silicon impregnation treatment to ensure that carbon produced by carbonization of the resin totally reacts with silicon to generate silicon carbide, thus obtaining the C/SiC composite material. The obtained C/SiC composite material is high in density, low in air pore and free silicon content, and favorable in material strength, toughness and frictional wear performance, and can be used for manufacturing of brake pads.

Provided is a waterborne ultra-thin steel structure fire retardant coating and a preparation method thereof. The raw material ratio of the coating includes 15-50% by weight of polymer latex, 15-30% by weight of ammonium polyphosphate, 5-15% by weight of pentaerythritol, 3-10% by weight of cyanurtriamide, 5-12% by weight of titanium dioxide, 2-13% inorganic filler, 0-5% by weight of expansiveness graphite, 1-10% by weight of plasticizer, 0.4-1.5% by weight of wetting dispersant, 0.2-0.5% by weight of defoamer, 1-6% by weight of coalescing agents and 5-15% by weight of water, and total raw material ratio is 100%. A high-speed dispersion method or a grinding dispersion method is adopted in preparation of the coating. A coating layer of the fire retardant coating can form a carbonization layer which is good in foaming effect, small and uniform in air holes and high in expansion times when in heating. The final fire retardant performance of the coating is far higher than technical requirements of a national standard. The waterborne ultra-thin steel structure fire retardant coating is a waterborne coating product, is non-poisonous and odorless and environment-friendly, and can be coated in a mode of brushing or spraying or roller coating.

The invention discloses a coking furnace capable of recycling heat energy, and the coking furnace comprises a furnace body, an exhaust gas recycling system and a raw coal gas treatment system, wherein the furnace body sequentially comprises a coal feeding segment, a rapid coal heating segment, a raw coal gas leading-out segment, a coal carbonization coking segment, a coke quenching and tempering segment, a dry coke quenching segment and a coke discharging segment from top to bottom; the exhaust gas recycling system comprises an exhaust gas leading-out unit, an exhaust gas heat exchanger, a commutator and the like; and the raw coal gas treatment system comprises a raw coal gas leading-out unit. By using the coking furnace disclosed by the invention, continuous coal carbonization coking canbe achieved and the exhaust gas after combustion is used for dry coke quenching in the furnace; pre-dried coal can be quickly heated to 300 DEG C during entering the furnace, the coal is carbonized and coked in the furnace body, and the exhaust gas generated by self-combustion is used for dry coke quenching at the furnace bottom after the exhaust gas is cooled by heat exchange with air, thus continuously producing coke; the pollution is less in the production process; the coal industrial chain is extended, the coking cost is lowered, the coking coal types are broadened, and the product quality is improved; the profit margins are expanded in a large extent; and the maintenance cost is low.

The invention provides a method for preparing a porous silicon/carbon composite material by using diatomite as the raw material, which is characterized by comprising the following steps of: with the diatomite as the raw material, performing simple refinement and purification processing to obtain silicon with a porous structure by means of metallothermic reduction; performing mechanical ball-milling with the carbon materials and/or precursors of carbon, hydro-thermal carbonization, pyrolytic carbonization or chemical vapor deposition to prepare the porous silicon/carbon composite material. Thecomposite material can be directly used as the cathode of the lithium ion battery, or can be mixed with other cathode materials to be used as the cathode materials of the lithium ion battery. Compared with a pure silicon material as the cathode material of the lithium ion battery, the porous silicon/carbon composite material has the advantages that the first reversible capacity and the circulation stability of the material are greatly improved. In the method, the inexpensive and accessible natural minerals are used as the raw materials, thus the cost is low and the preparation method is simple.

The invention relates to a method for preparing polyacrylonitrile-based carbon fiber with reinforced carbon nanometer tubes, which comprises the following steps: respectively dispersing and dissolving carbon nanometer tubes (CNT) and polyacrylonitrile (PAN) in dissolvent, obtaining PAN/CNT spinning solution through mixing the solution, obtaining PAN/CNT fiber through carrying out the wet-spinning method to the solution, then carrying out pre-oxidation and carbonization to the wet-spinning fiber to prepare the carbon fiber with reinforced carbon nanometer tubes. The mechanical property of the carbon fiber which is prepared by the method of the invention is obviously improved, and the prepared carbon fiber can be applied to the fields of reinforcing materials, conducting, electrostatic resistance, heat conducting and the like.

The invention discloses a method for preparing fewer-layer graphene on the basis of biomass waste, which comprises the following steps: carrying out hydrothermal treatment on the biomass waste, and carrying out carbonization by heating and calcination, thereby obtaining a carbonization material; immersing the carbonization material in an acid solution to remove impurities, thereby obtaining biomass carbon; and quickly heating the biomass carbon in an argon atmosphere, and carrying out high-temperature graphitization to obtain the biomass fewer-layer graphene. The hydrothermal process is combined with the high-temperature graphitization to directly strip the biomass waste, and the carbonization and high-temperature graphitization are carried out. Thus, the prepared biomass fewer-layer graphene has the advantages of fewer layers (2-10 layers), fewer defects, fewer oxy groups, high electric conductivity and small carbon layer interval. The method is simple to operate, has the advantages of low cost and high graphene yield, and can easily implement industrialized large-scale production. The prepared biomass fewer-layer graphene can be used in the fields of lithium ion batteries, supercapacitors and the like, is beneficial to green production of battery industry, and has important practical value and favorable application prospects.

The invention discloses a method for manufacturing a high thermal conductivity graphite film, which adopts polyimide films as raw materials and is formed through two processes of carbonization and graphitization. The technological processes of the high thermal conductivity graphite film comprise the steps as follows: a, the polyimide films are selected as the raw materials, and a piece of graphite paper is clamped between each layer of the polyimide films; b, the polyimide films which are provided with the graphite paper at intervals, crossed and stacked are placed into a carbonization furnace to be carbonized in an environment of nitrogen or argon, the carbonized temperature ranges from 1000 DEG C to 1400 DEG C, and the time is controlled from 1 hour to 6 hours; and c, after the carbonization, the graphitization is performed also in the environment of nitrogen or argon, the temperature is controlled in a range from about 2500 DEG C to 3000 DEG C, and the time is controlled within 12 hours. The method for manufacturing the high thermal conductivity graphite film has a simple manufacturing process, the high heat dissipation capacity of the graphite film is guaranteed, the bending-resistant performance is enhanced, and a requirement for a thin and light electronic product of a consumer is met to a certain extent.

A carbonization process for increasing the quality of wood by continuous gradient heating method includes such steps as heating to 120-140 deg.C, eating to 160-240 deg.C, spraying atomized water for slowly cooling to 100 deg.C, filling the saturated steam at 100 deg.C to return the water content back to 4-6%, and cooling to 15-30 deg.C.

The invention discloses technology for producing compressed and carbonized poplar three-layer solid wood composite floor fully through utilization of a fast-growing material of poplar. A poplar sheet obtained by a special densification process is used as a surface layer; a common poplar core veneer is used as a core layer; a poplar veneer is used as a bottom layer to manufacture three-layer solid wood composite floor; each performance reaches the requirement of national standard GB/T 18103-2000 on the solid wood composite floor; the technology totally adopts the fast-growing material of the poplar as a raw material, does not add any chemical reagent in the special densification process of the poplar sheet, and does not cause any pollution to environment; after the poplar sheet is subjected to compaction treatment, the density and the hard sense of the wood are strengthened; the late high-temperature carbonization treatment solves the problem of rebounding after the poplar is compressed, changes luster of the wood, and strengthens high grade; and the technology is simple and feasible and has low manufacturing cost.

The invention provides a silicon-carbon composite cathode material for preparing a lithium-ion battery at the room temperature and a preparation method thereof. The composite cathode material is a material with a nuclear shell structure and comprises the following proportional elements: 0.01-10% of simple substance silicon and 90-99.9% of carbon. With regard to the preparation method, silicon powder and graphite are mixed for ball grinding and then added with bitumen or polymer cladding material for ball grinding again, after the treatment of carbonization, the mixture is crushed and sieved to obtain the material containing 0.01-10wt% of silicon and 10-99.9% of carbon. The capacity of the material is more than 350mAh/g, the cycle efficiency of the material is larger than 90% for the first time, and keeps larger than 80% after 200 cycles, and the material has good charging and discharging property.

A method of forming a pyrolysed biocarbon from a pyrolyzable organic material is delineated. The method involves the conversion of pyrolyzable organic materials to biocarbon for subsequent use. A carbonization circuit is employed with individual feedstock segments being advanced through the circuit. The method facilitates user manipulation of rate of advancement of the feedstock through the circuit, selective collation of volatiles from pyrolyzing feedstock, selective exposure of predetermined feedstock segments to collated volatiles as well as thermal recovery and redistribution as desired by the user. This results in the capacity for a customizable biocarbon product, the latter being an auxiliary feature of the methodology.

A carbonization catalyst for forming graphene may be exfoliated from a graphene sheet by etching. A binder layer may be formed on the graphene sheet on which a carbonization catalyst is formed, to support and fix all or part of the graphene sheet. Further, the graphene sheet from which the carbonization catalyst is exfoliated may be transferred to a device. When exfoliating the carbonization catalyst from the graphene sheet, an acid may be used together with a wetting agent.

The invention discloses a refractory high-entropy alloy/titanium carbide composite. A refractory high-entropy alloy serves as a matrix phase, and titanium carbide serves as a wild phase; and elements in the refractory high-entropy alloy are selected from at least four kinds of elements of W, Mo, Ta, Nb, V, Ti, Zr, Hf and Cr. A preparation method of the refractory high-entropy alloy/titanium carbide composite comprises the steps that at least four kinds of carbonization metal powder in tungsten carbide, molybdenum carbide, tantalum carbide, niobium carbide, vanadium carbide, the titanium carbide, hafnium carbide, zirconium carbide and chromium carbide are selected and mixed according to the equal molar ratio or the ratio close to the equal molar ratio to form high-entropy matrix powder; and after the high-entropy matrix powder and titanium powder are mixed, alloy mechanization is carried out, then spark plasma sintering or hot-press sintering is carried out, and the refractory high-entropy alloy/titanium carbide composite is obtained. The density and cost of the composite are reduced while the hardness of the composite is improved, excellent high-temperature performance is achieved, and the requirement for manufacturing a high-temperature structural component is met.

The invention provides a densification method for a carbon fiber reinforced silicon carbonitride ceramic composite material. The method comprises the following steps: firstly, preparing a C/SiC ceramic composite material by using CVI or PIP; performing CVI on the C/SiC ceramic composite material to carbonize silicon, and as the cross gap between fiber bundles is large, prolonging the CVI time to 20-30 hours ; when the silicon being subjected to carbonization is densified to 80-90% by CVI, brushing silicon powder on the C/SiC surface, and filling large holes particularly; performing nitridation processing after drying; after completion of the nitridation, preparing an SiC coating on the CMC surface through CVD for 20-30 hours to complete the densification of the carbon fiber reinforced silicon carbonitride ceramic composite material. Through the adoption of the densification method, the CMC preparation efficiency is improved, the coefficients of thermal expansion of matrixes are reduced, and the thermal shock resistance of CMC is improved.

The invention discloses a method for preparing charcoal activated carbon flammable gas biological oil by utilizing crop straws. In the method, a co-production process technique integrated with comprehensive processing of multiple varieties is adopted. The method comprises the following steps: smashing the collected crop straws by a smash machine so as to form straw powder with the particle size of 8-30 meshes; pressing and forming the straw powder material for pyrolysis; and in the process of pyrolysis, preparing straw charcoal and activated carbon on one production line through carbonization and activation processes, and simultaneously, recovering flammable gas and extracting biological oil. By using the method, fixed investment is greatly reduced, economic and social benefits are effectively increased, the problems of stack and incineration of the straws are solved, waste straw resources are further developed and utilized, and the blank in the same industry in China is filled.

The invention discloses a method for preparing 5-hydroxymethylfurfural by solid acid catalysis. The method comprises the following steps of taking lignin residue hydrolyzed by biomass as carrier raw material of solid acid; synthesizing the raw material into solid acid through a two-step way of carbonization and sulfonation, so that the waste material is recycled and the problem of disposal of pollutants is solved. In the dehydration reaction of lignin-based solid acid catalyzed fructose and glucose, the yield of 5-hydroxymethylfurfural can be respectively 84% and 68%; after the dehydration reaction, the lignin-based solid acid is easy to separate and reusable, the acid density of the solid acid can be reduced after being reused five times, and the yield of the 5-hydroxymethylfurfural is still higher than 75%. The method provided by the invention can be used for realizing emission without pollution, and is helpful for realizing environment-friendly producing process of 5-hydroxymethylfurfural.

Methods for making porous articles are described, along with articles and structures which can be made by these methods. The methods typically involve polymerization of a carbon-containing precursor in the presence of an amphiphilic molecular structure, followed by carbonization to make a final product. Articles of the invention are generally porous, carbon-containing, and can have one or any number of features including crystallinity, electrical conductivity, and porosity of a specific and advantageous nature.

(Problem)

In conventional method for producing artificial graphite, in order to obtain a product having excellent crystallinity, it was necessary to mold a filler and a binder and then repeat impregnation, carbonization and graphitization, and since carbonization and graphitization proceeded by a solid phase reaction, a period of time of as long as 2 to 3 months was required for the production and cost was high and further, a large size structure in the shape of column and cylinder could not be produced. In addition, nanocarbon materials such as carbon nanotube, carbon nanofiber and carbon nanohorn could not be produced.

(Means to Solve)

A properly pre-baked filler is sealed in a graphite vessel and is subsequently subjected to hot isostatic pressing (HIP) treatment, thereby allowing gases such as hydrocarbon and hydrogen to be generated from the filler and precipitating vapor-phase-grown graphite around and inside the filler using the generated gases as a source material, and thereby, an integrated structure of carbide of the filler and the vapor-phase-grown graphite is produced. In addition, nanocarbon materials are produced selectively and efficiently by adding a catalyst or adjusting the HIP treating temperature.

The present invention discloses a method for preparing heteroatom doped carbon quantum dot, and application thereof in fields of biomedicine, catalysts, photoelectric devices, etc. The various kinds of heteroatom doped carbon quantum dots are obtained by using a conjugated polymer as a precursor and through a process of high temperature carbonization. These carbon quantum dots contain one or more heteroatoms selected from the group consisting of N, S, Si, Se, P, As, Ge, Gd, B, Sb and Te, the absorption spectrum of which ranges from 300 to 850 nm, and the fluorescence emission wavelength of which is within a range of 350 to 1000 nm. The carbon quantum dot has a broad application prospect in serving as a new type photosensitizer, preparing drugs for photodynamic therapy of cancer and sterilization, photocatalytic degradation of organic pollutants, photocatalytic water-splitting for hydrogen generation, organic polymer solar cell and quantum dot-sensitized solar cell.

The invention discloses a silicon-carbon composite cathode material with a three-dimensional preformed hole structure and a preparation method thereof. According to the composite cathode material, a carbon material having high electric conductivity and a stable structure is used as a matrix for dispersedly containing high-volume silicon particles, and proper three-dimensional expansion spaces are reserved around one or several silicon particles. The preparation method comprises the following steps of: carrying out surface modification on the silicon particles; coating the silicon particles by silicon dioxide; coating the silicon dioxide/silicon composite particles by carbon source precursors; carrying out high-temperature carbonization treatment; and removing a silicon dioxide template, and the like. When the composite material prepared by the preparation method is used for a lithium ion battery, the reversible specific capacity is high, and the cycle performance is excellent. The silicon-carbon composite cathode material has the advantages of simple preparation process and wide raw material resource and is suitable for industrial production.

A method is provided for carbonizing and activating carbonaceous material, which comprises supplying the material to an externally fired rotary kiln maintained at carbonizing and activating temperatures, the kiln having a downward slope to progress the material as it rotates, the kiln having an atmosphere substantially free of oxygen provided by a counter-current of steam or carbon dioxide, and annular weirs being provided at intervals along the kiln to control progress of the material. There may further be provided an externally fired rotary kiln for carbonizing and activating carbonaceous material having a hollow rotary body that has a downward slope towards a discharge end thereof, and which is provided at intervals along its length with annular weirs for controlling progress of the carbonaceous material. In embodiments, there is also provided a process is for producing discrete solid beads of polymeric material e.g. phenolic resin beads having a mesoporous structure, which may be useful as feedstock for the above mentioned carbonization/activation process or which may have other utility e.g. as ion exchange resins. The process may produce resin beads on an industrial scale without aggregates of resin building up speedily and interrupting production. The process comprises the steps of: (a) combining a stream of a polymerizable liquid precursor e.g. a novolac and hexamine as cross-linking agent dissolved in a first polar organic liquid e.g. ethylene glycol with a stream of a liquid suspension medium which is a second non-polar organic liquid with which the liquid precursor is substantially or completely immiscible e.g. transformer oil containing a drying oil; (b) mixing the combined stream to disperse the polymerizable liquid precursor as droplets in the suspension medium e.g. using an in-line static mixer; (c) allowing the droplets to polymerise in a laminar flow of the suspension medium so as to form discrete solid beads that cannot agglomerate; and (d) recovering the beads from the suspension medium. There is also provided apparatus for forming discrete solid beads of polymeric material, said apparatus comprising: a first line for conveying s stream of a polymerizable liquid precursor; a second line for conveying a stream of a dispersion medium with which the polymerizable liquid precursor is substantially or completely immiscible; an in-line mixer configured to receive a combined flow from the first and second lines and to disperse the polymerizable liquid precursor as droplets in the dispersion medium; a vertical polymerization column configured to receive the dispersion medium with the droplets dispersed therein and to permit the polymerizable liquid precursor polymerize while descending the column in a descending flow of polymerization medium; and a vessel at the base of the column for receiving the descending flow of dispersion medium and collecting polymerized solid beads.

The invention discloses a method for manufacturing a SiC ceramic-based turbine blade based on photocurable 3D printing. The method comprises the following steps of firstly manufacturing a turbine blade resin mold based on the photocurable 3D printing technology, casting the blade resin mold by using a non-water-based gel-casting ceramic slurry, curing and carrying out pyrolysis carbonization process to obtain a porous carbon preform; by an in-situ reaction sintering technology, at 1420-1700 DEG C, carrying out siliconizing and silicon discharge processes on the carbon perform to obtain the porous SiC ceramic-based composites material turbine blade; and finally obtaining the dense SiC ceramic-based composites material turbine blade by a chemical vapor deposition/infiltration method. The method has the characteristics of near-net molding, free molding and complex molding and the purpose that ceramic parts are densified can be achieved at a lower temperature.

The invention provides a method for preparing active porous graphene. The method comprises the following steps: 1) bleaching cellulose by use of hydrogen peroxide to obtain a first intermediate product; 2) activating the first intermediate product by use of an activating agent to obtain a second intermediate product; 3) performing carbonization treatment on the second intermediate product at 600-1100 DEG C to obtain the active porous graphene. The invention aims to provide a method for preparing active porous graphene, and the active porous graphene prepared from the method provided by the invention has better conductivity and has better dispersity.

The present invention discloses a hot-pressing carbonization strengthening method of timbers, which includes drying, planing, hot-pressing carbonization, cooling and other steps. The present invention applies a hot press as a timber-carbonizing device, and the timbers under the state of compression are processed by hot-pressing carbonization. The present invention is characterized in that the investment on carbonization devices is less, the carbonization process is simple, the production is safe, the production efficiency is high, the consumption of heat energy is little, and the production cost is low; moreover, the thickness of the carbonized timbers is not limited, the defects of the timbers, such as deformation, cracking, stiker stain, color difference, knot fall-off, etc., do not occur in the process of production, so the quality of products is high; not only is the size stability and noncorrodibility of the carbonized timbers improved, but also the density and mechanical property of the timbers is increased.

The invention discloses a preparation method of an anode material for a power lithium ion battery. The preparation method comprises the following steps: by adopting petroleum coke ground until the grain size is 1-6mu m, calcined petroleum coke or needle coke as a raw material, adding additives, adding a mixture to a reaction kettle to carry out first high-temperature carbonization coating under the protection of the inert atmosphere, then grinding the mixture with a grinder until the grain size is 5-13mu m, then carrying out superhigh-temperature graphitization at a temperature above 3200 DEG C, adding one or a mixture of petroleum asphalt, coal asphalt and resin to a material obtained after graphitization, and then enabling the mixture to enter a carburization furnace to undergo second coating under the protection of the inert atmosphere to obtain the anode material for the power lithium ion battery, namely a spheroidal artificial graphite material which is formed through bonding after being coated with granules and undergoes two-time coating and three-time high-temperature treatment. The preparation method has the advantages that the discharge rate property of the anode material is improved, the low temperature properties of the anode material are improved, and the latest requirements of the market for the product are further met.

The invention relates to a coal-fired power plant coal dust prepared activated coke flue gas comprehensive purification system and a technology. The technology provided by the invention comprises the following steps of: using coal dust in a coal-fired power plant as a raw material, simultaneously carrying out carbonization and activation on coal dust in an activated coke preparation reactor to obtain powdered activated coke, using pyrolysis gas obtained during the preparation process as reburning fuel and sending it into a boiler so as to remove part of NOx; sending the powdered activated coke into a flue gas adsorption tower, adsorbing pollutants such as sulfur dioxide, mercury and the like at an appropriate temperature, injecting ammonia gas and nitrogen oxide to perform a catalytic reduction reaction so as to remove nitrogen oxide; reusing the adsorbed activated coke after regeneration; sending the activated coke into the boiler for combustion after multiple adsorption/regeneration; regenerating the activated coke after adsorbing sulfur dioxide to obtain high-density sulfur dioxide gas to realize resource utilization. By the utilization of coal resources in a coal-fired power plant, the comprehensive purification of flue gas and the resource utilization of sulfur dioxide are realized without discharge of waste water, exhaust gas and solid waste.

The invention discloses a silicon-carbon composite material with nano micropores and a preparation method as well as application thereof. The material comprises nano-silicon (Si) particles and a carbon nanofiber matrix, wherein the nano-silicon particles are dispersed in the carbon nanofiber matrix; and nano pores and micropores communicated with the nano pores are distributed in the carbon nanofiber matrix. The method comprises the steps of dissolving the nano-Si particles and polyacrylonitrile (PAN) in a solvent to prepare a mixed spinning solution, then carrying out electrostatic spinning on the mixed spinning solution, and curing spinning trickles in a coagulating bath to obtain a porous PAN-Si composite nanofiber; and then carrying out oxidation and carbonization treatment in sequence to obtain the silicon-carbon composite material with a nano micropore structure. The silicon-carbon composite material is applied to preparation of lithium ion battery cathode materials. Compared with the prior art, the silicon-carbon composite material ensures the overall electron transport capacity of the material while reserving buffer space for expansion of the nano-Si particles.