805 results about "Oxide composite" patented technology

The invention relates to the technical field of gas detection, in particular to a multi-gas accurate detection method and system.The method comprises the following steps that gas to be detected flows through a miniature gas enrichment device prepared through an MEMS technology under driving of a miniature gas pump, and target gas is adsorbed and enriched through graphene and metal oxide composite sensitive materials on the surface of a spiral gas inlet flow channel in the miniature gas enrichment device; the desorption concentrated gas is heated to the multi-gas composite detector, and the sensor array reacts with the gas to generate an electric signal; the data acquisition unit performs noise reduction, amplification and analog-to-digital conversion preprocessing on the electric signal; the data processing unit extracts characteristic vectors such as a response curve peak value and a rising slope; inputting the feature vector into a pre-trained machine learning classification-regression combined model, and outputting a gas type identifier and an initial concentration; error compensation is carried out in combination with environment temperature and humidity and a cross sensitivity interference mode library, and finally accurate information of at least nine gases is output. The device has the advantages of high sensitivity, strong anti-interference performance and miniaturization.

The invention provides a polyaniline / modified graphene oxide composite material and a preparation method thereof. The preparation method comprises the following steps: dispersing purified graphene oxide, performing ultrasonic treatment, heating, adding a modifier for modification, centrifuging, taking precipitate, freezing, drying and grinding to obtain modified graphene oxide powder; mixing the powder with an aniline solution in doped acid to form a modified graphene oxide / aniline acid solution; dissolving ammonium persulfate in the doped acid to prepare an ammonium persulfate acid solution; and slowly dropwise adding the solution into the solution, carrying out in-situ polymerization, and carrying out suction filtration, washing and drying to obtain the composite material. According to the method, through chemical modification and in-situ polymerization processes, the problems that a single filler is poor in dispersity, a conductive network is discontinuous, and anti-corrosion and anti-static performance is difficult to synergistically improve are solved, and the process is simple and convenient and suitable for industrialization.

According to the Pt cluster catalyst, the preparation method and the application, an aluminum oxide composite metal oxide carrier is prepared by adopting a pH swing method, a defect oxide nano island is formed through high-temperature reduction treatment, and oxygen vacancies contained on the surface can firmly anchor a subsequently loaded Pt cluster, so that the coking phenomenon of the Pt-based catalyst is reduced, and the catalytic activity of the Pt-based catalyst is improved. The catalytic activity and the stability of the Pt cluster catalyst are obviously improved. Meanwhile, Pt clusters are prepared through a heating reflux method, so that the Pt clusters have high dispersity and rich active sites, the finally prepared Pt cluster catalyst is small in Pt particle size and high in atom utilization rate, and when the Pt cluster catalyst is used for catalyzing a dehydrogenation reaction of a liquid organic hydrogen carrier, the Pt cluster catalyst is weak in adsorption capacity to a product, and the catalytic activity of the liquid organic hydrogen carrier is improved. The catalyst can show high conversion rate and hydrogen release rate at low temperature, can still keep stable structure at high temperature, and provides an efficient and reliable solution for engineering application of an LOHC dehydrogenation link.

The invention relates to a sludge biochar modified layered bimetallic oxide, and a preparation method and application thereof. The modified layered bimetallic oxide is prepared from the following main raw materials: domestic sewage aeration tank sludge, NaOH, Na2CO3, FeCl3. 6H2O and MnCl2. 4H2O. The domestic sewage aeration tank sludge is used for preparing dry sludge, the ferric chloride solution and the manganese chloride solution are used for preparing sludge composite layered double hydroxides, and the final layered bimetallic oxide composite sludge biochar catalyst can be prepared by calcining the sludge composite layered double hydroxides. The modified layered bimetallic oxide prepared by the scheme of the invention can effectively degrade bisphenol A, has relatively strong reusability, and still keeps good degradation ability in a relatively wide pH environment.

The invention relates to the field of fiber production, and particularly discloses a zinc oxide antibacterial ES fiber and a preparation method thereof. The zinc oxide antibacterial ES fiber comprises a core layer and a surface layer, and the surface layer comprises the following raw materials in parts by weight: 80-100 parts of polyethylene, 2-5 parts of a nano-zinc oxide composite material, 1-2 parts of a dispersing agent and 2-3 parts of a compatilizer; the nano-zinc oxide composite material is prepared from hydroxyapatite nanowires, a polyethylene glycol solution and coated nano-zinc oxide in a mass ratio of 1: (8-10): (1.5-2); the preparation method comprises the following steps: melting the material of the core layer to obtain a melt; mixing polyethylene, the nano-zinc oxide composite material, a dispersing agent and a compatilizer, and melting to obtain a polyethylene melt; and mixing the melt and the polyethylene melt, spinning, bundling, stretching, carrying out heat setting, curling and cutting off to obtain a finished product, the fiber has the advantages of being good in antibacterial property, high in mechanical strength, good in spinning stability and good in air permeability.

The invention belongs to the field of interface evaporation materials, and provides an interface evaporation material loaded with PDA / rGO photo-thermal hydrogel and a preparation method of the interface evaporation material. The PDA / rGO photo-thermal hydrogel loaded interface evaporation material is composed of a sponge material and PDA / rGO photo-thermal hydrogel loaded on the sponge material, and the PDA / rGO photo-thermal hydrogel is composed of calcium alginate hydrogel and a polydopamine / reduced graphene oxide composite material loaded in a polymer network of the calcium alginate hydrogel. The polydopamine / reduced graphene oxide composite material is prepared from reduced graphene oxide and polydopamine combined on the surface of the reduced graphene oxide; the interface evaporation material takes a sponge material as a porous skeleton, the PDA / rGO photo-thermal hydrogel is attached to the porous skeleton, and the interface evaporation material has a porous structure. According to the invention, the long-term use stability and evaporation flux of the existing hydrogel-based interface evaporation material can be improved.

The invention provides a wastewater advanced oxidation catalyst and a preparation method and application thereof, the wastewater advanced oxidation catalyst is of a core-shell structure, the core is activated carbon containing copper oxide and optional ferrous sulfide, and the shell is a silicon oxide-aluminum oxide compound containing nano ferrous sulfide. The invention further provides a preparation method of the wastewater advanced oxidation catalyst and application of the wastewater advanced oxidation catalyst in organic wastewater treatment. The wastewater advanced oxidation catalyst has the characteristics of high catalytic degradation capability on organic pollutants and the like, solves the problem of copper dissolution, and improves the long-term effectiveness of the catalyst.

The invention discloses a silicon / graphite / carbon-aluminum oxide composite negative electrode material and a green preparation method thereof, and belongs to the technical field of lithium ion batteries. Aiming at the problems of high volume expansion rate and poor cycling stability of a silicon-based negative electrode and high cost of a traditional process, the invention innovatively provides the following scheme: 1) waste photovoltaic silicon wafer ball-milling liquid and waste graphite are taken as core raw materials, and resource recycling is realized; (2) phenolic resin and chitosan are adopted as double carbon sources, a nitrogen-doped carbon layer (the nitrogen content is 3-5 wt.%) is formed through pH-induced self-assembly, and the conductivity and the Li < + > diffusion rate are synchronously improved; and 3) aluminum nitrate is introduced for pyrolysis to generate 2-5nm aluminum oxide for doping, so that the side reaction of the electrolyte is inhibited, and the volume expansion of silicon is relieved (the expansion rate is less than or equal to 120%). The preparation process comprises the steps of silicon / graphite dispersion, double-carbon-source compounding, ammonia water regulation and control precipitation and gradient calcination. Experiments show that the specific capacity of the optimized material under the current of 0.5 A / g reaches more than 800mAh / g, the 100-time cycle capacity retention ratio is more than 98%, the 1000-time cycle capacity retention ratio is more than 80%, the reversible specific capacity under the multiplying power of 3A / g is more than 550mAh / g, and the raw material cost is reduced by 40%. The invention has the advantages of high capacity, long service life, environmental protection and economy, and provides an innovative solution for the fields of power batteries and energy storage.

The invention relates to the technical field of soil remediation, in particular to a charcoal-fungus symbiont for a freeze-thaw environment and a preparation method and application of the charcoal-fungus symbiont. The preparation method of the charcoal-fungus symbiont comprises the following steps: crushing a biomass raw material, and carrying out pyrolysis to prepare basic charcoal; placing the basic biochar in an iron oxide solution, and carrying out an iron oxide loading reaction to obtain iron oxide biochar; the preparation method comprises the following steps: dipping iron oxide biochar in a chitosan solution for coating modification, then continuously adding a cross-linking agent for cross-linking solidification, and freeze-drying to obtain chitosan-iron oxide composite modified biochar; and immersing the chitosan-iron oxide composite modified biochar into a bacterial suspension of functional microorganisms, oscillating and adsorbing, and freeze-drying to obtain the carbon-bacteria symbiont. The invention aims to improve the heavy metal pollution phenomenon of soil and the soybean root rot disaster in the freezing and thawing cycle environment at the same time.

The invention relates to a preparation method of an etching-resistant and wear-resistant Y2O3-AlxOy composite coating. The preparation method comprises the following steps: carrying out ultrasonic cleaning on a corrosion-resistant matrix; performing plasma bombardment cleaning activation on the surface of the corrosion-resistant matrix; a Y2O3 coating and an AlxOy coating are alternately deposited on a corrosion-resistant base body in a double-target magnetron sputtering mode to form the Y2O3-AlxOy composite coating, the sputtering power of a Y target is larger than that of an Al target, and the ratio of x to y in the AlxOy coating is larger than 1. According to the method, the amorphous AlxOy coating dominated by the metal state is introduced into the Y2O3 coating, growth of Y2O3 columnar crystals is continuously broken, crystal grains are refined, formation of intergranular easy-to-etch point locations is inhibited, and an yttrium aluminum oxide composite strengthening phase is formed at an interface, so that plasma etching resistance is improved; the thickness of a single-layer coating in the composite coating is very thin; under the action of growth stress, the structure of the coating presents a wave-shaped microstructure and a soft and hard alternate mechanical structure, and the soft and hard alternate mechanical structure is beneficial to inhibiting generation of transverse cracks, guiding friction crack level expansion, prolonging the friction life of the coating and reducing the wear rate.

According to the emulsion mixing equipment applied to the mixing field and used for aluminum oxide composite fiberboard production, through a guide cylinder which forms an annular gap with the inner wall of a tank body in an enclosing mode and a stirring assembly arranged on the lower portion of the guide cylinder, raw materials circularly flow between the annular gap and an inner cavity of the guide cylinder, and the stirring assembly and a shearing assembly act synergistically; firstly, raw materials fully flow, components are promoted to be uniformly dispersed, local concentration difference is avoided, a foundation is laid for stable emulsification, agglomeration and precipitation are reduced, the emulsification efficiency and quality are improved, meanwhile, by means of a plurality of heat exchange structures such as a tank shell wall cooling clamping cavity, a spiral heat exchange pipe, an emulsification stator inner heat exchange channel and a guide cylinder shell wall spiral channel, sufficient heat exchange is achieved, and the emulsification efficiency and quality are improved. The raw material temperature is effectively controlled, heat accumulation and overheating are reduced, and the gelation probability is reduced.

The invention relates to an electrolytic copper foil anode plate electrode and a preparation process thereof, and belongs to the technical field of electrolytic copper foil production. The electrolytic copper foil anode plate electrode sequentially comprises a titanium substrate, an Ir-Ta oxide transition layer and an IrO2-RuO2-SnO2 oxide composite coating from inside to outside. The preparation process comprises the following steps: firstly, forming a micron-sized rough surface by utilizing acetone and ethanol ultrasonic cleaning and oxalic acid etching; the transition layer is subjected to sol dispersion and sintering treatment through polyethylene glycol, so that the balance of low porosity and high bonding strength is realized; the composite coating adopts an acetylacetone-ethylene glycol monomethyl ether solvent system, and a nanocrystalline structure is formed through step-by-step sintering; and an Ir-rich passivation layer is generated through electrochemical activation, and the finally obtained anode plate electrode has more excellent electrochemical activity and longer service life.

The invention discloses a two-dimensional metal oxide composite reduced graphene oxide burning rate catalyst, which is prepared by the following steps: uniformly grinding glucose, ammonium nitrate and transition metal nitrate, calcining at high temperature to generate a two-dimensional metal oxide nanosheet, mixing the two-dimensional metal oxide nanosheet with surfactant modified reduced graphene oxide powder, and sintering at high temperature to obtain the two-dimensional metal oxide composite reduced graphene oxide burning rate catalyst. And transferring into a high-pressure hydrothermal kettle for solvothermal reaction, so that the reduced graphene oxide and the two-dimensional metal oxide nanosheet are compounded to form the composite burning rate catalyst with a 2D-2D structure. Two two-dimensional materials are compounded through a solvothermal method, the defects of accumulation of reduced graphene oxide and aggregation of the two-dimensional metal oxide due to high surface energy are effectively avoided, meanwhile, the high conductivity of the reduced graphene oxide is utilized, the synergistic catalysis effect of the metal oxide and the carbon material is enhanced, and the performance of the composite material is improved. The composite material has a good catalytic effect on the thermal decomposition process of ammonium perchlorate.

The invention discloses a modified MoS2 / graphene oxide composite material and a preparation method thereof. The preparation method comprises the following steps: modifying commercial MoS2 by using a silane coupling agent to enable the commercial MoS2 to be positively charged, and then self-assembling with negatively charged graphene oxide to obtain the modified MoS2 / graphene oxide composite material. When the composite material is added into an epoxy resin solid coating as an additive, the friction coefficient can be effectively reduced, and the corrosion resistance can be improved.

The invention discloses a high-entropy oxide composite negative electrode material as well as a preparation method and application thereof, and relates to the technical field of all-solid-state lithium battery negative electrode materials, and the high-entropy oxide composite negative electrode material comprises a metal element and an oxygen element, the high-entropy oxide composite negative electrode material comprises a metal element and an oxygen element, wherein the metal elements are at least five of a chromium element, an iron element, a nickel element, a manganese element, a molybdenum element, a copper element and a cerium element; the molar ratio of the metal element to the oxygen element is 3: 4; the high-entropy oxide composite negative electrode material is of a spinel structure. According to the prepared high-entropy oxide composite negative electrode material, the problems that a traditional negative electrode material is unstable in structure, poor in interface contact and short in cycle life are solved, the electrochemical performance is improved, and an all-solid-state lithium battery prepared from the high-entropy oxide composite negative electrode material shows high reversible specific capacity and excellent cycle stability.

The invention relates to the technical field of brake discs, in particular to a carbon-ceramic brake disc with a composite functional layer and a preparation method of the carbon-ceramic brake disc. The problems that a brake disc is insufficient in strength and poor in ablation resistance are solved. The preparation method comprises the following steps: carrying out low-temperature plasma treatment and silicon dioxide sol impregnation on carbon fibers, and inserting a graphene oxide film between woven layers, so as to obtain a carbon fiber preform; primary densification is carried out through pretreatment activation, low-temperature permeation and high-temperature permeation, and two graphitization treatments are combined; siliconizing is carried out through low-pressure permeation, high-pressure strengthening and laser cladding, and secondary densification is carried out through precursor impregnation and cracking; the titanium zirconium silicide-nano aluminum oxide composite layer generated through the embedding process forms a compact oxidation film at high temperature, and the silicon carbide nano crystal whiskers are subjected to chemical vapor deposition, so that the strength and ablation resistance of the prepared carbon ceramic brake disc are improved.

The invention discloses a sulfur iron oxide composite denitrification filler, a preparation method and application, and relates to the technical field of sewage treatment, the sulfur iron oxide composite denitrification filler comprises sulfur powder, siderite, magnesite, magnesium oxide, metal manganese, metal aluminum, nano iron, boric sludge, magnetite and a binder; wherein the sum of the addition amounts of the metal manganese, the metal aluminum and the nano iron accounts for 8-16% of the mass of the sulfur-iron oxide composite denitrification filler. The technical problems that in the prior art, strength and abrasion resistance are insufficient, and denitrification efficiency is low are solved.

The invention provides a preparation method and application of graphene in-situ growth CNT composite conductive slurry. The preparation method comprises the following steps: adding a sodium hydroxide solution into a graphene oxide composite salt solution for reaction, and performing suction filtration after the reaction is completed to obtain a graphene oxide composite catalyst; repeatedly cleaning with deionized water, drying, firing at high temperature, and crushing to obtain a catalyst; the preparation method comprises the following steps: putting a catalyst into a CVD (Chemical Vapor Deposition) tubular furnace, carrying out high-temperature reaction under the protection of inert gas in the whole process, sequentially introducing reducing gas and carbon source gas to obtain coarse carbon nanotube powder, and then carrying out high-temperature oxidation purification in air to obtain high-purity CNT powder; the preparation method comprises the following steps: fully dissolving a dispersant in a solvent, adding high-purity CNT powder, stirring, and carrying out high-pressure homogeneous dispersion. The graphene oxide is selected as a carrier of the carbon nanotube catalyst, so that the activity of the catalyst and the growth multiple of the carbon nanotube are improved, and the carbon nanotube powder with good conductivity is prepared on the surface of the graphene.

The invention discloses a preparation method of a Fe3O4 / reduced graphene oxide composite wave-absorbing material, and belongs to the technical field of electromagnetic wave absorbing materials. According to the method, the interface interaction between Fe3O4 and reduced graphene oxide is enhanced through a freeze drying process, the density of the material is reduced, the degree of reduced graphene oxide is further improved by cooperating with post-treatment, and the method for preparing the Fe3O4 / graphene composite material is low in cost, simple and environmentally friendly.

The invention discloses a metal element doped MnO2 and MnFe oxide composite catalyst as well as a preparation method and application thereof, and belongs to the technical field of flue gas desulfurization and denitrification. The preparation method comprises the following steps: dissolving potassium permanganate, divalent manganese salt and doped metal salt in water for reaction to prepare metal element doped MnO2; and mixing and reacting with a template agent, ferric salt and sodium salt, drying and roasting to obtain the final catalyst. The MnO2 electronic structure is modulated by doping metal elements, and the three-dimensional porous structure of the MnFe oxide is constructed by using the template agent, so that the catalyst has efficient adsorption and strong catalytic oxidation capacity, NO and SO2 can be synergistically removed at the same time, and the catalyst has desulfurization and denitrification activity in a wide temperature range of 30-300 DEG C, and is suitable for industrial production. And liquid ammonia does not need to be used in the purification process, so that the purification agent is high in safety and is particularly suitable for purification treatment under complex flue gas conditions in the non-electric industry.

The invention discloses a sulfide-oxide composite solid electrolyte based on Lewis acid-base reaction, a preparation method of the sulfide-oxide composite solid electrolyte and a battery, and relates to the technical field of solid-state batteries. Comprising a sulfide electrolyte and a composite coating coated on the surface of the sulfide electrolyte, and the composite coating comprises an oxide electrolyte and a Lewis alkaline substance. The oxide electrolyte and the Lewis alkaline substance are adopted as the composite coating material, so that the sulfide electrolyte can be isolated from air, the air stability of the sulfide electrolyte is effectively improved, and the phenomenon that the sulfide electrolyte is subjected to oxidation-reduction decomposition in the charge-discharge process is reduced; and by-products generated in the use process of the sulfide electrolyte can be neutralized in situ by the Lewis alkaline substance, so that the great increase of interface impedance is reduced, the cycle performance and high-current stability of the battery are remarkably improved, and the problem that the interface impedance is increased in the charge-discharge process of the traditional sulfide solid electrolyte is solved.

The invention discloses a preparation method of a wear-resistant magnetic composite nano ferroferric oxide material, and belongs to the technical field of nano ferroferric oxide materials.The preparation method comprises the steps that coated modified ferroferric oxide composite powder, silver nitrate and absolute methanol are added into a reaction kettle, stirring and ultrasonic dispersion are conducted, then 2-aminoterephthalic acid is added, stirring and mixing are conducted, and a mixture is obtained; and after the reaction, separating to obtain the wear-resistant magnetic composite nano ferroferric oxide material. The wear-resistant magnetic composite nano ferroferric oxide material prepared by the preparation method disclosed by the invention overcomes the problem that an existing ferrite material is relatively single in electromagnetic loss mechanism in the aspect of nickel-phosphorus plated fabric, and the electromagnetic shielding effectiveness of the fabric is improved; the coated modified ferroferric oxide composite powder has good dispersity, a polydopamine coating layer on the surface of the coated modified ferroferric oxide composite powder improves the anchoring effect on silver MOF particles through a mussel-like adhesion interface, meanwhile, stress is dispersed and crack propagation is reduced through the buffering effect of the polydopamine coating layer, and the mechanical stability of the wear-resistant magnetic composite nano ferroferric oxide material is improved.

The invention relates to the technical field of manganese zinc ferrite materials, and particularly discloses a manganese zinc ferrite high-frequency high-impedance material and a preparation process thereof. The manganese zinc ferrite high-frequency high-impedance material is prepared from the following raw materials: Fe2O3, Mn3O4, ZnO, a carbon nanotube loaded rare earth oxide composite material, P2O5, Co2O3 and CaCO3. The preparation raw materials of the carbon nanotube loaded rare earth oxide composite material comprise a multi-walled carbon nanotube and a rare earth salt, and the mass ratio of the multi-walled carbon nanotube to the rare earth salt is 1: (0.12-0.14). According to the invention, the loss capability of the manganese zinc ferrite material to electromagnetic interference is enhanced, and the problem that the magnetic conductivity and impedance of the material are reduced in a high-frequency environment is solved.

The invention relates to the technical field of metal surface coating preparation, in particular to a high-temperature thermal cycle impact resistant yttrium oxide composite coating on the surface of refractory metal and a preparation method of the yttrium oxide composite coating. The refractory metal composite coating material is composed of a refractory metal matrix and a coating. The coating comprises a bonding layer, a middle layer and a surface layer which are arranged in a contact manner; the bonding layer is composed of the refractory metal and yttrium oxide, and the porosity of the bonding layer is 1%-5%; the middle layer is a pure yttrium oxide layer with the porosity of 5%-10%; the porosity of the surface layer is 1t; 2% of a pure yttrium oxide layer; the melting point of the refractory metal is 2470 DEG C or higher. According to the refractory metal composite coating material and the preparation method and application thereof, the refractory metal coating structure is optimized, the porosity of the coating is further adjusted, the high-temperature molten metal corrosion resistance and the high-temperature thermal shock resistance of the coating are improved, meanwhile, the bonding strength between the coatings is guaranteed, and the service life of the coating is prolonged. The method is expected to be applied to high-melting-point metal smelting equipment.

The invention relates to a preparation method of an oxygen vacancy-rich bismuth molybdate / bismuth vanadate composite photo-anode and a product and application thereof, and belongs to the technical field of photoelectrocatalysis. The invention discloses a preparation method of an oxygen vacancy-rich bismuth molybdate / bismuth vanadate (Bi2Mo2O9 / BiVO4) composite photo-anode, which mainly comprises the following steps: immersing a fluorine ion-doped tin dioxide (FTO) conductive glass substrate into a Bi < 3 + > ion solution and an I <-> ion solution to form a bismuth oxyiodide (BiOI) film, dropwise adding a dimethyl sulfoxide solution of vanadyl acetylacetonate (VO (acac) 2), and putting into a muffle furnace to prepare the BiVO4 photo-anode. And then vertically immersing into a Bi < 3 + > ion solution and a Mo < 6 + > ion solution, and carrying out annealing treatment in an argon atmosphere to prepare the Bi2Mo2O9 / BiVO4 composite photoanode rich in oxygen vacancies. The Bi2Mo2O9 / BiVO4 material rich in oxygen vacancies is a metal oxide composite photo-anode, the photoelectrocatalysis efficiency can be improved, and hydrogen peroxide (H2O2) can be continuously generated in natural seawater through photoelectrocatalytic oxidation of water for a long time.

The invention discloses a nickel-tin alloy-oxide composite material Ni3Sn2-NiSnOx, a preparation method thereof and application of the nickel-tin alloy-oxide composite material Ni3Sn2-NiSnOx in electrocatalytic ammonia synthesis reaction, and belongs to the technical field of electrochemical catalysis. The preparation method comprises the following steps: adding SnCl2. 2H2O and NiCl into deionized water as raw materials, adding glycine, potassium pyrophosphate and urea as electro-deposition auxiliary agents, and stirring for 10 minutes to obtain electro-deposition liquid; and carrying out electro-deposition on a conductive substrate serving as a cathode, so that Ni and Sn are co-deposited to form a nickel-tin alloy, and part of the nickel-tin alloy reacts with oxygen in the deposition process or after deposition to form a nickel-tin oxide phase, so that the Ni3Sn2-NiSnOx composite catalytic material is obtained. By regulating and controlling the concentration of tin ions in the electroplating solution and the electrodeposition time, the component proportion of nickel and tin in the product and the morphology structure of the material can be regulated. The composite material provided by the invention has excellent electrocatalytic nitrogen reduction synthesis ammonia activity and selectivity, and solves the problems that the service life of a catalyst is shortened and the catalytic activity and stability are reduced due to irreversible reconstruction of an alloy compound under high potential.

The invention discloses a preparation method of a manganese-doped iron-based sulfide / nitrogen-doped reduced graphene oxide composite electrode material for a sodium-ion battery, a simple solvothermal method is combined with annealing treatment, and iron atoms in a hexagonal system are replaced by part of manganese atoms in a hydrothermal process to form multivalent iron-based sulfide, so that the composite electrode material is prepared. The manganese-doped iron-based sulfide / nitrogen-doped reduced graphene oxide composite electrode material for the sodium-ion battery is successfully prepared by uniformly compounding the manganese-doped iron-based sulfide and the nitrogen-doped reduced graphene oxide, and the manganese-doped iron-based sulfide / nitrogen-doped reduced graphene oxide composite electrode material can effectively regulate and control the electronic state density, reduce the sodium ion migration energy barrier and promote the electron / ion transmission; meanwhile, continuous growth of iron-based sulfide particles is limited, so that the iron-based sulfide particles are uniformly dispersed on the surface of the graphene, more active sites are exposed, the electrochemical reaction activity is improved, and the structural stability is enhanced. The composite electrode material disclosed by the invention can be widely applied to a negative plate for a sodium-ion battery, and has excellent adaptability and application prospect in a wide temperature range and under a high-current working condition.

The invention provides a bacteriostatic proppant technology based on a palladium oxide-reduced graphene oxide composite material, aiming at the problem of hydrogen loss caused by microbial activity in a hydrogen storage bank of an exhausted gas reservoir. A PdO (at) rGO composite material functionally modified by lead ions (Pb < 2 + >) is loaded on the surface of a porous ceramsite carrier to form an adsorption-inactivation-blocking synergistic antibacterial network; precise laying of the proppant in a crack network is achieved through the end sand removal technology, hydrogen consumption is reduced, and an efficient, economical and environment-compatible innovative solution is provided for biological pollution control of the underground hydrogen storage library.

The invention provides a modified high-temperature-resistant heat-insulating anticorrosive coating and a preparation method thereof. The modified high-temperature-resistant heat-insulating anticorrosive paint comprises a component A and a component B, the component A comprises organic silicon resin, epoxy resin, a polyaniline-nano metal oxide-graphene oxide composite material, hollow glass beads and hexagonal boron nitride; the component B comprises an organic silicon modified amine curing agent, an anhydride curing agent, a titanate catalyst and an accelerant. The modified high-temperature-resistant heat-insulating anticorrosive paint has excellent corrosion resistance, high-temperature-resistant heat-insulating performance and high-temperature cracking resistance, and also has the advantages of strong adhesive force and short surface drying time. The modified high-temperature-resistant heat-insulating anticorrosive paint provided by the invention is suitable for corrosion protection of metal components exposed in high-temperature and complex corrosive environments for a long time.

The invention discloses organic silicon modified acrylic resin antifouling paint and a preparation method thereof, and particularly relates to the field of chemical paint. The antifouling paint is prepared from the following components in parts by mass: 8 to 12 parts of adamantane acrylate, 5 to 8 parts of trifluoroethyl acrylate, 2 to 3 parts of 2-hydroxyethyl acrylic phosphate, 0.8 to 1.2 parts of tert-butyl peroxypivalate, 4 to 6 parts of tridecafluorooctyltrimethoxysilane, 1 to 2 parts of isophorone diisocyanate, 3 to 6 parts of fluorosilane modified nano TiO2 and 1 to 2 parts of graphene oxide. 20-30 parts of deionized water, 0.5-1 part of a polyether modified polysiloxane defoaming agent, and 0.3-0.5 part of an ultraviolet light absorber UV-327 can be additionally added. The preparation method comprises the following steps: S1, preparing isocyanate modified fluorine-containing organic silicon; s2, preparing a ternary copolymer prepolymer; s3, preparing a modified resin matrix; s4, preparing a fluorosilane modified nano TiO2 / graphene oxide composite filler dispersion liquid; and S5, mixing the resin matrix and the dispersion liquid, and performing stirring and vacuum desolventizing to obtain a finished product. The coating has the characteristics of super-hydrophobicity, high hardness, strong adhesion, long-acting antifouling property, aging resistance and environmental protection.