33results about How to "Uniform specific surface area" patented technology

The invention relates to a zinc oxide medium and high temperature coal gas fine desulfurizer and a preparation method, belonging to the technical field of the preparation and the application of desulfurizers, in particular to the preparation and the application of zinc oxide medium and high temperature coal gas fine desulfurizers. The zinc oxide medium and high temperature coal gas fine desulfurizer is characterized by having wide sources and high price and can finely remove sulfureted hydrogen at medium and high temperature (300-550 DEG C) in the strongly reducing atmosphere. The active ingredients of the desulfurizer are uniformly distributed on a carrier surface and have the particle diameter of 10-400 nm. In the preparation method, the two steps of semicoke carrier modification and the active ingredient dipping are combined into one step, the two functions for improving the carrier hole structure and loading the components can be synchronously finished in an autoclave. The semicoke has wide sources, high price and simple preparation technique; the prepared desulfurizer can finely remove sulfureted hydrogen at medium and high temperature in the strongly reducing atmosphere, hasbetter thermal stability, and can be widely used in the field of desulfurizing and purifying the reducing chemical virgin gas which is prepared by using coal as materials.

The invention discloses an ATP / g-C3N4-Ag composite material with high visible-light activity, and a preparation method and application thereof. According to the invention, attapulgite having undergone coating modification by a g-C3N4 thin layer is used as a substrate; Ag nano-particles are deposited on the prepared ATP / g-C3N4 thin layer in situ via a chemical reduction method; and due to good synergism among attapulgite, the g-C3N4 thin layer and the Ag nano-particles, the novel efficient stable ATP / g-C3N4-Ag composite material is obtained. The composite material prepared in the invention presents excellent photocatalysis performance, can reduce cost and pollution and has good application prospects and economic benefits in treatment of water pollution.

The invention discloses a fertilizer capable of enhancing grape quality. The fertilizer is prepared from the following raw materials in parts by weight: 20-35 parts of potassium nitrate, 5-15 parts of double superphosphate, 16-24 parts of kiln ash potassium fertilizer, 8-15 parts of rotten chicken manure, 40-60 parts of fermented bean dregs, 12-18 parts of cotton seed pulp, 8-16 parts of straw powder, 10-16 parts of wormcast, 2-6 parts of modified illite-montmorillonite clay, 2-4 parts of carbonized corn cob powder, 15-35 parts of plant ash, 1-4 parts of meerschaum powder, 1-4 parts of vermiculite powder, 1-2 parts of diatomite, 0.5-1 part of manganese humate, 0.5-1 part of ferrous sulfate, 0.04-0.09 part of composite bacterium and 1-3 parts of Chinese herbal medicine additive. The fertilizer has balanced nutrients, and pays attention to the nitrogen / phosphorus / potassium mixing ratio, so that the grapes can quickly and sufficiently acquire the nutrients in various growth periods, thereby ensuring the normal growth of roots, leaves, flowers, fruits and the like of the grapes, enhancing the yield and quality of the grapes and being beneficial to yield increase and income increase.

The invention relates to a high-activity TiO2 nanometer pipe / intermediate phase carbon microsphere composite material and a preparation method and application thereof. The high-activity TiO2 nanometer pipe / intermediate phase carbon microsphere composite is obtained by depositing TiO2 nanometer pipes on surfaces of intermediate phase carbon microspheres performed with alkali activating treatment in a hydrothermal method. The obtained high-activity TiO2 nanometer pipe / intermediate phase carbon microsphere composite has large specific surface area and strong adsorption / desorption performance, is used as electrode materials of a super capacitor, remarkably improves the specific surface area, utilization rate, specific capacitance and conducting performance of electrode materials in aqueous electrolyte and organic electrolyte and prolongs service life of the super capacitor. Further the preparation method of the high-activity TiO2 nanometer pipe / intermediate phase carbon microsphere composite has the advantages of being easy in process, low in manufacture cost and the like, and raw materials are low in price.

The invention relates to a preparation method of non-carbon fuel battery catalyst carrier WO3 (Tungsten Trioxide) with high stability by using a silicon oxide molecular sieve as a template. According to the preparation method, the silicon oxide molecular sieve is used as the template, a metal precursor is dipped into a silicon oxide pore passage, and the silicon oxide template is removed through etching after steps of evaporations, roasting and the like, so as to obtain the porous metallic oxide WO3 with controllable appearance. The non-carbon fuel battery catalyst carrier WO3 has excellent stability when being used as a fuel battery catalyst carrier.

The invention discloses a composite base fertilizer for grapes. The composite base fertilizer comprises the following raw materials in parts by weight: 50-70 parts of fermented chicken manure, 14-22 parts of edible mushroom dregs, 20-26 parts of biogas digester dregs, 14-22 parts of fishbone dust, 16-24 parts of sunflower seed meal, 10-20 parts of monopotassium phosphate, 25-40 parts of ammonium nitrate, 20-28 parts of potassium fulvic acid, 20-40 parts of a kiln dust potassium fertilizer, 4-8 parts of carbonized coconut shell powder, 3-7 parts of sepiolite powder, 4-8 parts of kieselguhr, 1.5-2.5 parts of seashell powder, 4-8 parts of modified illite-montmorillonoid clay, 1-2 parts of fulvic acid diamine iron, 2-3 parts of fulvic acid manganese, 4-6 parts of traditional Chinese herbal medicine additives and 0.1-0.2 part of compound bacteria. The composite base fertilizer is balanced in nutrition and focuses on the mixing ratio of nitrogen, phosphorus and potassium, grapes can take nutrient components rapidly and sufficiently in different growth periods, normal growth of roots, leaves, flowers, fruits and the like of the grapes can be ensured, the yield of the grapes can be increased, the quality of the grapes can be improved, and the yield and the income can be increased.

The invention belongs to the field of antioxygen, in particular to an emulsion antioxygen and a preparation method thereof. The emulsion antioxygen is emulsified and compounded by the following raw material reagents at the proportion: main antioxygen, auxiliary antioxygen, emulsifying agent, dispersing agent and defoaming agent. The emulsion antioxygen has better oxidation resistance than other similar antioxygens and can achieve the optimal oxidation resistance effect, and the total solid content of the emulsion antioxygen is more than 52%. The emulsion antioxygen has the advantages of good oxidation resistance effect, big activity, low volatility, high durability, no pollution and the like and is especially suitable for protecting tint and pollution-free color polymer thereof. The emulsion antioxygen can be favorably dispersed in ABS (Acrylonitrile Butadiene StyreneAcrylonitrile Butadiene Styre) rubber latex, is ideal antioxygen used preparing ABS by emulsion polymerization and has excellent dispersibility. According to the emulsion antioxygen, the heating oxygen aging time of the ABS resin can be prolonged in the ABS production, the oxidation inducing temperature of the ABS resin is improved, the phenomenon that the ABS resin becomes yellows in the production and processing process thereof can be prevented, the strength of a product can be improved, and the oxidation resistance problem for preparing ABS by emulsion polymerization can be solved.

The invention discloses a molecularly-imprinted nanoparticle for glycoprotein and a synthesis method thereof, belongs to the field of analytical chemistry, and relates to synthesis of molecularly-imprinted polymers. The synthesis method comprises the following steps: firstly, preparing a solution phase A from template glycoprotein molecules, preparing a solution phase B from a functional monomer and a cross-linking agent, and preparing solution phase C from an initiator; secondly, respectively fixing the solution phase A, the solution phase B and the solution phase C on three micro-fluidic injection pumps with adjustable flow rates, connecting and mixing the solution phase A and the solution phase B through a Y-shaped three-way valve, connecting and mixing the mixed solution and the solution phase C through another Y-shaped three-way valve, and enabling the obtained mixed solution and the solution phase C to flow into a reactor for a polymerization reaction; and finally, collecting a polymerized nanoparticle at the tail end of the reactor, and removing the glycoprotein template molecules to obtain the molecularly-imprinted nanoparticle for glycoprotein. The molecularly-imprinted nanoparticle for glycoprotein is prepared in a microfluidic mode, operation is easy, continuous production can be achieved, and the obtained molecularly-imprinted nanoparticle can be used for specific recognition of target glycoprotein molecules.

The invention discloses an aqueous-phase preparation method of bismuth sulfide / protein composite nanospheres. Mannitol is used as ligand, and the bismuth sulfide / protein composite nanospheres are prepared for the first time in an aqueous phase under room temperature condition. The prepared bismuth sulfide / protein composite nanospheres have characteristics of porous structure, large specific area, uniform shape, controllable size, low biological toxicity and the like, can be used as a biological medical probe and have potential application prospect in the medical imaging aspect such as CT. The method is simple in devices, moderate in condition, low in energy consumption, short in preparation period, easy to realize and is an ideal method for preparing a bismuth sulfide / protein composite nano material.

The invention belongs to the field of environment-friendly materials, and particularly relates to adsorption type bone apatite and a preparation method and application thereof. The preparation methodcomprises the following steps: removing organic matters in animal bones; calcining the animal bones without the organic matters to obtain bone apatite; and carrying out surface chemical modification on the bone apatite by adopting a phosphoric acid solution to obtain the adsorption type bone apatite. The adsorption type bone apatite can be used for adsorbing heavy metal ions in industrial sewage,and the specific surface area of the adsorption type bone apatite is increased from 47.832 (m<2> / g) to 131.566 (m<2> / g) compared with the specific surface area of the adsorption type bone apatite before modification; when the initial concentration of Pb<2> is 200 mg / L, a removal rate can reach 98.3%; for Zn<2> and Cu<2> ions with an initial concentration of 200 mg / L, the removal rate of the ions can reach 70% or above; so the adsorption type bone apatite has good heavy metal ion removal capacity. The technical problem that bone apatite in the prior art is not high enough in adsorption capacityis solved.

The invention discloses a preparation method of TNT magnetic molecularly imprinted polymer microspheres. The method comprises the steps of: firstly adopting 3-aminopropyltriethoxysilane to perform amination modification on surfaces of Fe3O4 nanoparticles, then dispersing the aminated Fe3O4 nanoparticles in acetonitrile, adding a template molecule TNT and functional monomer acrylamide, performing prepolymerization, adding a cross-linking agent ethylene glycol dimethacrylate and an initiator azobisisobutyronitrile so as to prepare magnetically imprinted polymer microspheres, and finally performing elution treatment on the microspheres to obtain the TNT magnetic molecularly imprinted polymer microspheres. By combining technologies of molecular imprinting with magnetic separation, the preparedpolymer particles have a uniform shape and uniform size, the specific surface area of the TNT molecularly imprinted polymer microspheres is increased, and good adsorption and separation performance are achieved, wherein the adsorption amount is about 2.6 times that of a traditional embedding method, the separation time is about 1 / 5 of that of the embedding method, and specific adsorption of TNT is achieved.

The invention belongs to the field of materials, and relates to vanadium trioxide nanoparticles. The vanadium trioxide nanoparticles are spheroidic, have the particle size range of 50-100 nm and have the specific surface area of 120.4+ / -0.1 square meters per gram. The invention also provides a preparation method for the vanadium trioxide nanoparticles, wherein the method includes the steps: adding commercially available vanadium pentoxide to ethylene glycol, and stirring and mixing uniformly, to form a suspension A; adding hydrochloric acid to the suspension A, to form a suspension B with the pH of about 1; heating the suspension B, and allowing to stand at room temperature and cooling, to obtain a product containing a dark blue precipitate; and carrying out centrifugal separation of the mixed solution of the product containing the deep blue precipitate, washing and drying, and thus obtaining the spheroidic nanoparticles. The vanadium oxide nanoparticles have quite high specific surface area and relatively strong structural stability, and are helpful to improve the performance of electronic materials and catalysts.

The invention relates to a method for detecting amaranth in food by using porous graphene, belonging to the field of analytical chemistry or food safety. According to the invention, porous graphene is prepared by using a metal etching method; dispersion liquid of porous graphene is dispensed on the surface of a glassy carbon electrode so as to prepare a porous graphene modified glassy carbon electrode; and since porous graphene has a large specific surface area, high conductivity, strong adsorption capability and good mass transfer effect, the porous graphene modified glassy carbon electrode is used for detecting amaranth in food in experiments. The detection method provided by the invention has the advantages of high sensitivity, low detection limit, easiness and accurate results.

The invention specifically relates to a benzene hydrorefining catalyst, and a preparation method and application thereof, belonging to the technical field of benzene hydrorefining catalysts. The preparation method comprises the following steps: S1. Uniformly mixing raw materials for a carrier of the benzene hydrorefining catalyst, carrying out extrusion granulation, and then carrying out sinteringmolding at 680 to 700 DEG C to obtain the carrier; S2, adding phosphoric acid into water with a temperature of 46-50 DEG C, carrying out uniform mixing, then carrying out heating to 88-92 DEG C, adding cobalt carbonate for a reaction, then adding molybdenum trioxide after gas release of the reaction is completed, and then carrying out mixing and dissolving to obtain an activation solution; S3, placing the carrier in an enclosed reactor, and carrying out multi-stage high-temperature activation; and S4, carrying out cooling to room temperature to obtain the benzene hydrorefining catalyst. According to the invention, phosphoric acid and rare earth metals are added into the benzene hydrorefining catalyst, so dispersion of the active component molybdenum is facilitated, the specific surface area of the catalyst is larger and more uniform, and active sites are increased; moreover, the preparation method is simple and employs a multi-stage high-temperature activation manner for activation, so the water content of the catalyst is reduced, the water resistance of the catalyst is improved, and the service life of the catalyst is prolonged.

The invention discloses a crude benzene hydrorefining catalyst and a preparation method thereof. The catalyst consists of a pre-hydrogenization catalyst and a main hydrogenization catalyst, wherein the pre-hydrogenization catalyst is obtained by performing surface modification on active aluminum oxide serving as a carrier by adding rare elements, then soaking the active aluminum oxide in a molybdenum and nickel solution and performing activation; the main hydrogenization catalyst is obtained by performing surface modification on active aluminum oxide and titanium dioxide which serve as carriers by adding rare elements, then soaking the carriers in a molybdenum and cobalt solution and performing activation. By the adding of phosphoric acid and rare earth metal, the catalyst disclosed by the invention is beneficial for dispersion of molybdenum serving as an active component, and the specific surface area is relatively large and uniform; the number of active points is increased; moreover, by the adding of the rare elements, the poisoning performance and the carbon deposition resistance of the catalyst are enhanced; by virtue of the preparation of the catalyst carriers and the adding of the titanium dioxide and the rare earth material, the use temperature range of the catalyst is enlarged, and the defect that the use temperature range of an existing catalyst is relatively small is effectively overcome.

The invention discloses a preparation method of an Ir nanowire with nano holes and an obtained material and application thereof. Deionized water is taken as a solvent, Ir salt is taken as a precursor,and PAH (polyacrylamide hydrochloride) is taken as a morphology guiding agent and a surface activating agent, the pH value of a mixed solution is adjusted to 6-14, a reducing agent is added, one-stepreduction is carried out by adopting a hydrothermal reaction method after uniformly mixing is carried out, and the product is centrifuged, washed and dried to obtain the Ir nanowire with the nano holes. Compared with a traditional preparation method, the operation of method is simple and rapid, the prepared and obtained Ir nanowire with the nano holes are uniform in morphology and cross-linked toform a plurality of branches, and large-scale production can be realized; the Ir nanowire with the nano holes prepared and obtained by the method has the advantages of being hollow, porous, large inspecific surface area, multiple in active sites, rich in surface defects, and has excellent electrocatalytic activity for the oxygen evolution reaction under an alkaline condition, and the Ir nanowirecan be applied to the catalyst of an alkaline oxygen evolution reaction.

The invention belongs to the field of environmental protection materials, and specifically relates to an adsorption-type bone apatite and its preparation method and application. During the preparation, the organic matter in the animal bone is removed; the animal bone from which the organic matter has been removed is calcined to obtain the bone apatite; The phosphoric acid solution is used to chemically modify the surface of the bone apatite to obtain the adsorbed bone apatite. The adsorption-type bone apatite of the present invention can be used to adsorb heavy metal ions in industrial sewage, compared with the specific surface area before modification from 47.832 (m 2 / g) increased to 131.566(m 2 / g); in Pb 2+ When the initial concentration is 200mg / L, the removal rate can reach 98.3%. For the initial concentration of 200mg / LZn 2+ 、Cu 2+ Ions, the removal rate can reach more than 70%, and it has good ability to remove heavy metal ions. The invention solves the technical problem of insufficient bone apatite adsorption capacity in the prior art.

The invention discloses a high-impact transparent permanent antistatic polypropylene composite material and a preparation method thereof. The high-impact transparent permanent antistatic polypropylenecomposite material comprises the following raw materials: polypropylene, functionalized ethylene propylene rubber, a transparent agent, an antioxidant and a nucleating agent. The polypropylene composite material prepared by melting, mixing and granulating the raw materials has the advantages of high impact resistance, excellent transparency, permanent static resistance and the like, can be applied to the fields of light diffusion LED illumination, food packaging, daily article packaging and the like, and is particularly applicable as a raw material for the packaging industry of direct injection molding and the like.

The invention discloses a modified soft carbon negative electrode material, a lithium ion battery, a negative electrode material and a preparation method. The preparation method of the modified soft carbon negative electrode material comprises the steps of sequentially carrying out activation treatment, washing, drying and heat treatment on a soft carbon carbonization precursor material, wherein the soft carbon carbonization precursor material is obtained by carbonizing a soft carbon precursor material at the temperature of 1250-1450 DEG C; the mass ratio of the soft carbon carbonization precursor material to an activating agent in the activating treatment process is 100: (3-15); the activating agent is an alkali metal-containing alkaline inorganic compound and / or chlorine-containing inorganic salt; and the temperature of the heat treatment is 500-700 DEG C. According to the modified soft carbon negative electrode material disclosed by the invention, the structure of the soft carbon isimproved, the amorphous degree of the soft carbon structure is improved, pore lithium storage sites of the soft carbon material are increased, lithium intercalation and deintercalation channels are increased, and the obtained modified soft carbon negative electrode material is high in initial reversible capacity, initial coulombic efficiency and capacity retention ratio after 100 cycles.

The invention discloses a method for simultaneously preparing iron phosphate (FePO4) with a micro-nano porous structure and 5-hydroxymethylfurfural (5-HMF), and an obtained material and application thereof. The method comprises the following steps: with deionized water and ethanol as solvents, a ferric iron salt and a phosphate radical-containing compound as raw materials and carbohydrate as a morphology guiding agent and a surfactant, conducting uniform mixing, performing one-step reduction by adopting a hydrothermal reaction method, filtering a product to obtain a liquid 5-HMF, and washing and drying a solid to obtain the iron phosphate with the micro-nano porous structure. Compared with a traditional preparation method, the method is simple, rapid and green to operate, the prepared ironphosphate with the micro-nano porous structure is uniform in morphology and has the micro-nano porous structure, and large-scale production can be achieved. The iron phosphate with the micro-nano porous structure prepared by the method has the advantages of porosity, large specific surface area and the like, has excellent electrochemical performance and can be applied to a positive electrode material of lithium ion battery. The liquid obtained by the reaction is 5-HMF with high purity, and can be used as a biological energy material.

The invention belongs to the field of materials and relates to vanadium trioxide nanoparticles. The vanadium trioxide nanoparticles are spherical in shape, have a particle size range of 50-100 nanometers, and a specific surface area of ​​120.4±0.1 square meters per gram. The invention also provides a method for preparing vanadium trioxide nanoparticles. The method includes: adding commercially available vanadium pentoxide into ethylene glycol, stirring and mixing evenly to form suspension A; adding hydrochloric acid to suspension A to form a pH of about Suspension B is 1; heat suspension B and let it cool at room temperature to obtain a product containing dark blue precipitate; centrifuge the mixed solution containing the product containing dark blue precipitate, wash and dry to obtain spherical nanoparticles. The vanadium oxide nanoparticles of the present invention have a high specific surface area and strong structural stability, which are helpful to improve their performance as electrical materials and catalysts.

The invention relates to a zinc oxide medium and high temperature coal gas fine desulfurizer and a preparation method, belonging to the technical field of the preparation and the application of desulfurizers, in particular to the preparation and the application of zinc oxide medium and high temperature coal gas fine desulfurizers. The zinc oxide medium and high temperature coal gas fine desulfurizer is characterized by having wide sources and high price and can finely remove sulfureted hydrogen at medium and high temperature (300-550 DEG C) in the strongly reducing atmosphere. The active ingredients of the desulfurizer are uniformly distributed on a carrier surface and have the particle diameter of 10-400 nm. In the preparation method, the two steps of semicoke carrier modification and the active ingredient dipping are combined into one step, the two functions for improving the carrier hole structure and loading the components can be synchronously finished in an autoclave. The semicoke has wide sources, high price and simple preparation technique; the prepared desulfurizer can finely remove sulfureted hydrogen at medium and high temperature in the strongly reducing atmosphere, hasbetter thermal stability, and can be widely used in the field of desulfurizing and purifying the reducing chemical virgin gas which is prepared by using coal as materials.

The invention discloses an amorphous carbon material, a preparation method thereof, a negative electrode material and a lithium ion battery. The preparation method includes the following steps: mixinga biomass material with conductive carbon black to obtain a mixture; heat-treating the mixture; and carbonizing the heat-treated mixture in an inert atmosphere, and grinding the carbonized product toobtain the amorphous carbon material. The preparation method provided by the embodiment of the present invention allows the spherical amorphous carbon material to be prepared, so the specific surfacearea of the amorphous carbon material is reduced, the mechanical properties and electrochemical properties of the amorphous carbon material are improved, and the energy crisis and environmental issues are effectively alleviated; and the preparation method of the amorphous carbon material has the advantages of simplicity, low device requirements and low preparation cost, so the amorphous carbonmaterial can be easily industrially produced and applied.

The invention relates to a method for detecting amaranth in food by using porous graphene, belonging to the field of analytical chemistry or food safety. According to the invention, porous graphene is prepared by using a metal etching method; dispersion liquid of porous graphene is dispensed on the surface of a glassy carbon electrode so as to prepare a porous graphene modified glassy carbon electrode; and since porous graphene has a large specific surface area, high conductivity, strong adsorption capability and good mass transfer effect, the porous graphene modified glassy carbon electrode is used for detecting amaranth in food in experiments. The detection method provided by the invention has the advantages of high sensitivity, low detection limit, easiness and accurate results.

The invention discloses a water-phase preparation method of bismuth sulfide / protein composite nanospheres. Mannitol is added as a ligand, and bismuth sulfide / protein composite nanospheres are prepared for the first time in the water phase at room temperature. The bismuth sulfide prepared by the invention / Protein composite nanospheres have the characteristics of porous structure, large specific surface area, uniform shape, controllable size, and low biological toxicity. They can be used as biomedical probes and have potential application prospects in medical imaging such as CT. The invention states The method has the advantages of simple equipment, mild conditions, low energy consumption, short preparation cycle and easy realization, and is an ideal method for preparing bismuth sulfide / protein composite nanomaterials.

The invention discloses a crude benzene hydrogenation refining catalyst and a preparation method thereof. The catalyst is composed of a pre-hydrogenation catalyst and a main hydrogenation catalyst, wherein the pre-hydrogenation catalyst uses activated alumina as a carrier, and rare earth elements are added to its surface Modified, then impregnated with molybdenum and nickel solution, and activated; the main hydrogenation catalyst uses activated alumina and titanium dioxide as the carrier, adding rare earth elements to modify its surface, and then impregnated with molybdenum and cobalt solution, activated. The invention adds phosphoric acid and rare earth metals to the catalyst, which is beneficial to the dispersion of molybdenum as an active component, so that the specific surface area is larger and more uniform, and the active points are increased. And the addition of rare earth elements enhances the anti-poisoning performance and anti-carbon deposition performance of the catalyst. The addition of titanium dioxide and rare earth materials in the preparation of the catalyst carrier increases the service temperature range of the catalyst, effectively improving the shortcoming of the existing catalyst with a relatively small service temperature range.

The invention discloses a method for preparing Ir nanowires with nanoholes and the resulting materials and applications. Deionized water is used as a solvent, Ir salt is used as a precursor, and PAH (polypropylene amine hydrochloride) is used as a morphology Directing agent and surfactant, adjust the pH value of the mixed solution to 6-14, add a reducing agent, mix evenly and use a hydrothermal reaction method for one-step reduction, centrifuge, wash and dry the product to obtain Ir nanowires with nanopores . Compared with the traditional preparation method, the method is simple and quick to operate, and the prepared Ir nanowires with nanoholes have a uniform shape and are cross-linked into multi-branches, which can realize large-scale production. The Ir nanowires with nanoholes prepared by the method of the present invention have the advantages of being hollow and porous, large specific surface area, many active sites, and abundant surface defects, and have excellent electrocatalytic activity for the oxygen evolution reaction under alkaline conditions, and can be Catalyst for alkaline oxygen evolution reaction.

The invention relates to a novel lamellar molybdenum disulfide based nano immunologic adjuvant as well as a preparation method and application thereof. The immunologic adjuvant is a product obtained by modifying a molybdenum disulfide nano lamina by using CpG and PEG. The preparation method comprises: performing ultrasonic treatment on the molybdenum disulfide nano lamina; then mixing the molybdenum disulfide nano lamina with CpG and PEG, and performing temperature controlled incubation in a swing bed; and performing centrifugation to remove free CpG and PEG. The nano immunologic adjuvant provided by the invention is small in particle size, uniform in size, and large in specific area, has relatively strong near-infrared region photo-thermal conversion capability, and can improve the secretion level of immune activation related cell factors to a great extent in combination with infrared laser irradiation. Moreover, the nano immunologic adjuvant provided by the invention has relatively low cytotoxicity. The nano immunologic adjuvant provided by the invention has the advantages of low raw material cost, simple preparation process, good repeatability, stable performance and the like.