748 results about "Cyclohexanes" patented technology

The invention relates to the technical field of nano materials, and particularly discloses a preparation method of surface modified nano calcium carbonate for a battery diaphragm coating. According to the method, the technical paths of microemulsion confinement crystal form regulation and control, gradient surface modification and boehmite compounding and porosity regulation and control are fused, and the functional nano calcium carbonate adaptive to the battery diaphragm coating is prepared. According to the technical scheme, limestone is used as a raw material, after calcination and digestion, the particle size of nano calcium carbonate is controlled through microemulsion carbonization (a cyclohexane-span 80-n-butyl alcohol system); a silane coupling agent KH560-KH570 is adopted for gradient modification to introduce an electrophilic functional group, boehmite is compounded to form a composite coating, and the porosity is regulated and controlled by adjusting the solid content in coating slurry and the coating speed. The method is stable in process and high in compatibility, and meets the requirements of diaphragm coatings of lithium ion batteries and solid-state batteries.

The invention discloses a wood-based composite phase-change material and a preparation method thereof, and belongs to the technical field of phase-change materials.The preparation method of the wood-based composite phase-change material comprises the following steps that wood is cut and then added into delignification liquid to be heated, the wood is taken out and washed with water, and delignified wood is obtained; the delignification wood is added into the modification liquid to be heated, and after being taken out, the delignification wood is washed and dried to obtain pretreated wood; mixing polyethylene glycol, citric acid and boric acid, heating and stirring to obtain a phase change material; dipping the pretreated wood into the phase change material for vacuum dipping, taking out and drying to obtain the phase change material. The modified liquid is prepared from an ethanol water solution, a modified filler, 2-(3, 4-cyclohexene oxide) ethyltrimethoxysilane and triethylamine. The delignification liquid and the modification liquid are adopted for pretreating the wood, so that the wood can be better firmly combined with the phase change material, leakage is prevented, and the finally prepared wood-based composite phase change material has excellent heat management capacity and stability.

The invention provides a flexible switching production method and equipment for low cis-polybutadiene rubber (LCBR), solution polymerized styrene-butadiene rubber (SSBR) and hydroxyl-terminated liquid polybutadiene rubber (HTPB), the flexible switching production equipment comprises an initiator production device and a polymerization unit, and the flexible switching production method comprises the following steps: mixing cyclohexane and n-hexane according to a volume ratio of 6.5: 3.5-7: 3, adding an initiator, and stirring to obtain a mixture; forming a mixed solvent; the method comprises the following steps: adding a monomer, an active agent, an initiator and a mixed solvent into a polymerization kettle 31 of a polymerization unit, and carrying out polymerization reaction to obtain a low-cis-polybutadiene, solution polymerized styrene-butadiene or hydroxyl-terminated liquid polybutadiene rubber solution; a novel protection initiator tert-butyl dimethyl siloxy propyl sodium is designed, and hydroxyl-terminated liquid polybutadiene rubber with a controllable structure is prepared through anionic living polymerization. According to the process, shutdown for kettle cleaning is not needed, the low cis-polybutadiene, the solution polymerized styrene-butadiene and the hydroxyl-terminated liquid polybutadiene rubber can be produced on the same polymerization device in a flexible switching manner, and the overall production efficiency is improved.

The invention relates to an aliphatic copolyester elastomer and a preparation method thereof, and belongs to the field of high polymer materials. The elastomer is prepared through a series ring-opening copolymerization reaction of epoxide and cyclic anhydride, and the method comprises the following steps: under the action of a metal-free catalyst (a phosphazene ligand P1-tert-octyl / triethyl boron system) and an initiator (terephthalyl alcohol), carrying out a series ring-opening copolymerization reaction on epoxide and cyclic anhydride, the preparation method comprises the following steps: reacting epoxide (such as epoxypropane and allyl glycidyl ether) with aliphatic anhydride (such as glutaric anhydride) in a xylene solvent to generate a polyester prepolymer retaining an active end; adding a second group of epoxide (such as cyclohexene oxide) and anhydride (such as tetrahydrophthalic anhydride and norbornene dianhydride), continuously reacting to form a block copolymer, and then crosslinking. The material performance can be regulated by changing the monomer combination, the atom economy is high, and the raw materials can be produced on a large scale. The process is simple and environment-friendly, and a new choice is provided for application of the degradable elastomer in the fields of medical treatment, environmental protection and the like.

The invention belongs to the technical field of drug synthesis, and particularly relates to an adamantane derivative as well as a synthesis method and application thereof. The adamantane derivative comprises an intermediate structural formula I, an intermediate structural formula II and an intermediate structural formula III, and the structural general formula is as follows: Linker is substituted or unsubstituted C6-C10 aroyl, R1 is hydrogen or C1-C6 alkyl, R2 is hydrogen, C1-C6 alkyl or a nitrogen-containing or nitrogen-free structural fragment, or the integral structure of R1R2 is N-substituted heterocyclic pentyl or heterocyclic cyclohexyl. According to the adamantane derivative provided by the invention, an adamantane structure is combined with part of groups of OAB-14, and a parent nucleus structure is changed, so that the drug activity is improved. The invention also provides a synthesis method of the compound, the obtained compound is screened through cell viability research, and the compound has a potential synergistic effect in the aspects of preventing influenza and treating Alzheimer's disease.

The invention discloses a copper-based catalyst for catalyzing partial hydrogenation of nitrocyclohexane to prepare cyclohexanone-oxime as well as a preparation method and application of the copper-based catalyst. The catalyst comprises a main active component and an auxiliary active component, the main active component is copper, the auxiliary active component is selected from one or more of titanium, vanadium, chromium, molybdenum, zirconium, cadmium, indium, tin, antimony, niobium, silver, iron, zinc, magnesium, aluminum, bismuth, manganese, lanthanum, gold or lead, the total molar ratio of the copper to the auxiliary active component is (100-1): 1, and the catalyst is prepared by adopting a coprecipitation method or a supported impregnation-coprecipitation method. And the process is simple and green. Under mild conditions, the catalyst can realize the conversion rate gt of nitrocyclohexane; the selectivity of cyclohexanone-oxime is greater than or equal to 99%, and the method is obviously superior to the existing non-noble metal system, and is low in cost, good in stability and suitable for industrial production of green synthesis of caprolactam.

The invention relates to the technical field of oil-displacing agents, in particular to a polyacrylamide-containing oil-displacing agent and a preparation method thereof.The polyacrylamide-containing oil-displacing agent is prepared from, by weight, 35-40% of functionalized polyacrylamide, 5-8% of loading filler, 2-3% of n-amyl alcohol, 5-7% of cyclohexane and the balance water; the polyacrylamide is subjected to functional modification, and the loading filler loaded with the zwitterionic surfactant is added, so that the oil-displacing agent can still keep a good synergistic effect in a complex high-temperature and high-salt environment, and a good oil-displacing characteristic is exerted.

The invention provides a diesel oil anti-wear agent and a preparation process thereof, and belongs to the technical field of diesel oil additives, and the preparation process comprises the following steps: mixing and stirring diisooctyl maleate and xylene, adding diethylenetriamine and deionized water, carrying out heating reaction, adding toluene, 4-(aminomethyl) pyridine and ethylene oxide, carrying out mixing reaction, filtering, washing, and drying to obtain the diesel oil anti-wear agent. The pyridinium-based polyester hollow capsule is prepared; the preparation method comprises the following steps: mixing xylene, catechol, ethylene phosphonic acid, ammonium persulfate and deionized water, heating, dispersing in cyclohexane, adding polyvinyl alcohol, octadecyl methacrylate and azodiisobutyronitrile, mixing and reacting to obtain catechol phosphonate nano colloidal particles; mixing and stirring the fatty acid ester solution, the oleoyl fluorocarbon copolymer and the pyridinium-based polyester hollow capsule, adding the catechol phosphonate nano colloidal particles, continuously stirring, performing ultrasonic treatment, and degassing to obtain the diesel oil anti-wear agent. The diesel oil antiwear agent can improve the antiwear property and demulsibility of the diesel oil antiwear agent.

The present disclosure relates to a crystalline form of trans-4-[1-(3-Chloro-phenyl)-7-methoxy-2,4-dioxo-3,4-dihydro-2H-pyrimido[5,4-c]quinolin-3-yl]-cyclohexanecarboxylic acid hydrochloride, methods of preparation, and its use as a therapeutic agent to treat inflammatory diseases.

The invention provides an acid-resistant and anti-pollution composite nanofiltration membrane as well as a preparation method and application thereof, and relates to the technical field of membrane materials. The preparation method comprises the following steps: soaking the surface of a support membrane with a mixed solution I; the mixed solution I is prepared from doxycycline, 4-aminopyridine and deionized water; pouring an oil phase solution into the surface of the soaked support membrane to carry out interfacial polymerization reaction; the oil phase solution is composed of 1, 3-benzene disulfonyl chloride and cyclohexane; and carrying out heat treatment on the support membrane after the interfacial polymerization reaction to obtain the acid-resistant anti-pollution composite nanofiltration membrane. According to the prepared composite nanofiltration membrane, doxycycline is selected as a water-phase monomer for the first time, meanwhile, 1, 3-benzene disulfonyl chloride is selected as an oil-phase monomer, 4-aminopyridine is selected as an additive, and the prepared composite nanofiltration membrane not only has acid resistance and pollution resistance, but also has high permeation flux and high separation performance.

The invention belongs to the technical field of medicine synthesis, and particularly relates to a memantine derivative and a synthesis method and application thereof. The memantine derivative comprises an intermediate structural formula I, an intermediate structural formula II, an intermediate structural formula III and a structural general formula, Linker is substituted or unsubstituted C6-C10 aroyl, R1 is hydrogen or C1-C6 alkyl, R2 is hydrogen, C1-C6 alkyl or a nitrogen-containing or nitrogen-free structural fragment, or the integral structure of R1 and R2 is N-substituted heterocyclic pentyl or heterocyclic cyclohexyl. According to the memantine derivative provided by the invention, a memantine group is combined with an OAB-14 partial structure to change a parent nucleus structure, so that the drug activity is improved. The invention also provides a synthesis method of the compound, and the obtained compound is used for treating Alzheimer's disease and Parkinson's disease.

The invention discloses tranexamic acid-polypeptide conjugate as well as a preparation method and application thereof, and belongs to the technical field of biology. The invention relates to a tranexamic acid-polypeptide conjugate or a salt thereof. The structure of the tranexamic acid-polypeptide conjugate is as shown in the following formula (I): TXA-Xaa1-L-phenylalanyl-D-arginyl-L-tryptophanyl-Xaa2-NH2 (I), wherein TXA-Xaa1-L-phenylalanyl-D-arginyl-L-tryptophanyl-Xaa2-NH2 (I) is shown in the description; wherein TXA is 4-(aminomethyl) cyclohexane carbonyl, and TXA is 4-(aminomethyl) cyclohexane carbonyl; xaa1 is a chemical bond, a neutral amino acid residue or a hydrophilic linker; xaa2 is a chemical bond, a neutral amino acid residue or a hydrophilic linker. The tranexamic acid-polypeptide conjugate or the salt thereof disclosed by the invention can simultaneously block two key signal channels for melanogenesis to achieve a synergistic effect of '1 + 1gt, 2', and further improve the inhibition effect on melanogenesis.

The invention discloses a deep embossing polyester facing film, a preparation method thereof and a polyester film facing plate. The polyester facing film is prepared from the following raw materials in percentage by weight: 10 to 20 percent of flame-retardant polyester and the balance of poly (1, 4-cyclohexanedimethanol terephthalate); the flame-retardant polyester is prepared by condensation polymerization of a first esterification product and a second esterification product in a mass ratio of (60-70): (20-30), the raw materials of the first esterification product comprise terephthalic acid and 1, 4-cyclohexanedimethanol in a molar ratio of 1: (1.05-1.3), and the raw materials of the second esterification product comprise a benzoxazine phosphate monomer and dihydric alcohol in a molar ratio of 1: (1.1-1.3). The benzoxazine phosphate chain segment is introduced into the PCT, so that the flame retardant property of the polyester facing film is remarkably improved on the basis of not keeping the mechanical property and the processability of the polyester material.

The present invention relates to a mixed ester of cyclohexane-1, 2, 4-tripropionic acid and a plasticizer composition comprising said mixed ester. The present invention relates to a plasticizer composition comprising a compound of formula (1) and at least one dialkyl terephthalate wherein the two alkyl groups in the dialkyl terephthalate each have 8 or 9 carbon atoms.

The present disclosure relates to a crystalline form of trans-4-[1-(3-Chloro-phenyl)-7-methoxy-2,4-dioxo-3,4-dihydro-2H-pyrimido[5,4-c]quinolin-3-yl]-cyclohexanecarboxylic acid hydrochloride, methods of preparation, and its use as a therapeutic agent to treat inflammatory diseases.

This invention belongs to the field of two-dimensional material preparation technology, and provides an MXene material and its preparation method. The preparation method of the MXene material includes: mixing a MAX phase precursor to be etched with an organic halide reagent and a morphology modifier, performing a solvothermal etching reaction, and after the reaction, washing and drying the resulting product to obtain the MXene material; wherein the organic halide reagent is triethylamine trihydrofluoride, triethylamine hydrochloride, or dichloroethylamine hydrochloride, and the morphology modifier is ethylene glycol, dimethyl sulfoxide, or cyclohexane. The method of this invention can effectively control the microstructure and pore structure of the MXene material.

This invention relates to a method for preparing hexamethylenediamine by hydrogenation of adiponitrile in the presence of a Raney nickel catalyst, wherein a Raney nickel catalyst modified by treatment with carbon monoxide or carbon dioxide in a liquid medium is used.

The invention relates to fluorine-containing epoxy acrylate and a preparation method thereof, in particular to fluorine-containing epoxy acrylate and a preparation method thereof. The problems that in the prior art, bonding of nano particles is not firm, and the transparency of a coating is poor are solved. The method comprises the following steps: dissolving tridecafluorooctyl methacrylate, glycidyl methacrylate, a KH-570 silane coupling agent and an initiator by using 1, 4-dioxane as a solvent, introducing high-purity nitrogen into a reaction container for a certain time to remove oxygen in the reaction container so as to prevent polymerization inhibition, controlling the reaction temperature and the stirring rate, and reacting for a certain time to obtain the tridecafluorooctyl methacrylate. Keeping the introduction of nitrogen; contacting the reaction system with oxygen, cooling and quenching the polymerization reaction; adding the reaction liquid into cyclohexane of which the weight is five times that of the reaction liquid to remove unreacted monomers; drying the purified product in a vacuum oven, and grinding into powder; and cleaning commercially available filter paper with acetone. The invention belongs to the technical field of acrylic resin synthesis and superhydrophobicity.

The application provides a method for synthesizing adiponitrile by selective ammoxidation of epoxycyclohexane. The purpose of the application is to simulate and optimize the process of synthesizing adiponitrile by one-step direct ammoxidation of epoxycyclohexane, and to develop a new type of multiphase composite metal vanadium-based oxide catalyst, which is composed of Co a V b P c Mo d MNOx / TiO2, the active elements of which include vanadium element V, cobalt element Co, phosphorus element P and molybdenum element Mo, M is an auxiliary metal element (Mn, Cr, Fe or Ni), N is an alkali metal (Na, K or Cs); the value range of a is 0.2-1.2; the value range of b is 0.8-1.5; the value range of c is 0.1-0.23; the value range of d is 0.07-0.35; x is the proportion of oxygen atoms required to meet the oxidation state of metal. The catalyst has the advantages of simple preparation, good cycle stability, high yield and the like. The yield and product purity of adiponitrile are improved, the energy consumption in the production process of adiponitrile is reduced, and a breakthrough is realized in the production technology of adiponitrile.

The invention discloses a system and a method for dehydrogenation of methyl cyclohexane by using a fuel cell. The system comprises an electrochemical dehydrogenation power generation unit which takes a solid oxide fuel cell as a reactor and is used for performing an electrochemical dehydrogenation reaction on methylcyclohexane to generate a dehydrogenation product containing toluene and simultaneously generating electric energy; the electrochemical hydrogenation unit takes a proton exchange membrane electrolytic tank as a reactor and is used for carrying out electrochemical hydrogenation reaction on toluene and hydrogen to generate methylcyclohexane; and in the material circulation loop, toluene generated by the electrochemical dehydrogenation power generation unit is at least partially conveyed to the electrochemical hydrogenation unit to serve as a reactant, and methylcyclohexane generated by the electrochemical hydrogenation unit is at least partially conveyed to the electrochemical dehydrogenation power generation unit to serve as a reactant. The electrochemical reaction path is used for replacing traditional thermocatalysis, the reaction efficiency is improved, the energy consumption is reduced, and the system is a green and efficient energy comprehensive utilization system.

The present invention provides a plasticizer composition and a resin composition comprising the same. The plasticizer composition according to the present invention comprises a cyclohexane-1, 2-diester-based substance and a citrate-based substance, and the plasticizer composition is environmentally friendly and has high stability and excellent basic properties.

The invention provides yellow glue resistant to corrosion of a plasticizer and a preparation method of the yellow glue. The yellow glue is prepared from a polyurethane prepolymer, a chloroprene rubber sheet, methyl methacrylate, benzoyl peroxide, an anti-aging agent, butanone, cyclohexane, dimethyl carbonate and tackifying resin. The polyurethane prepolymer is prepared from the following components in parts by weight: 10 to 14 parts of 1, 4-butanediol adipic acid polyester polyol, 4 to 8 parts of polycaprolactone polyol, 1 to 3 parts of diphenylmethane diisocyanate, 0.05 to 0.15 part of 1, 6-hexanediol, 1 to 2 parts of hydroxyethyl methacrylate, 0.01 to 0.03 part of organic bismuth catalyst and 75 to 80 parts of butanone. The polyurethane prepolymer with specific crystallization performance is synthesized through cooperation of polycaprolactone polyol and polyester polyol, and the yellow glue is endowed with excellent plasticizer corrosion resistance and low-temperature activation capacity. Active groups in the polyurethane prepolymer are subjected to graft copolymerization with the chloroprene rubber adhesive and MMA, and a plasticizer-resistant polyurethane chain segment is introduced into a molecular chain of the chloroprene rubber adhesive, so that a hard segment-soft segment alternating block structure is formed, and corrosion resistance and viscoelasticity are both considered.

A polyester-based polymer according to the present invention contains 30 mol% or more of cyclohexanedicarboxylic acid, dimethylcyclohexanedicarboxylate, or a combination thereof as a dicarboxylic acid component, and thus is environmentally friendly, has controlled softness, and has excellent quality and processability. In addition, the polyester-based polymer includes a linear C3-C6 alkanediol or the like as a diol component, thereby improving cold resistance, chemical resistance, and elasticity while having softness.

The invention discloses a supramolecular self-assembled fiber as well as a preparation method and application thereof in cells. The supramolecular self-assembled fiber is obtained by mixing a cis, cis-cyclohexane-1, 3, 5-triformyl hydrazine mother solution, a p-formylphenylboronic acid mother solution and a 5-(2-aminophenyl) tetrazole mother solution in a phosphate buffer solution; the application of the supramolecular self-assembled fiber in cells comprises the following steps: inoculating a pore plate with Haila cells, gently and horizontally shaking, culturing, washing, incubating in a complete DMEM (Dulbecco Modified Eagle Medium) solution of 5-(2-aminophenyl) tetrazole, and washing to obtain pretreated cells; and further incubating and washing the pretreated cells in a complete DMEM (dulbecco's modified eagle medium) solution containing cis, cis-cyclohexane-1, 3, 5-triformyl hydrazine and p-formylphenylboronic acid, so as to obtain the cells enriched with the boron element. Compared with a small molecular boron carrying agent, the supramolecular self-assembled fiber prepared by the invention realizes effective boron element enrichment, and has the advantages of high affinity to tumor cells, good stability and low biotoxicity.

The invention discloses a high-temperature-resistant liquid crystal polymer substrate for ultrathin flexible display, which belongs to the technical field of flexible display and comprises a modified liquid crystal polymer and a functional additive dispersed in the modified liquid crystal polymer. The modified liquid crystal polymer is prepared by polymerizing a monomer composition, and is specifically prepared from 38 to 42 parts of p-hydroxybenzoic acid, 28 to 30 parts of 4, 4 '-biphenol, 5.6 to 6.0 parts of terephthalic acid, 4.4 to 5.0 parts of 2, 6-naphthalic acid, 2.7 to 3.3 parts of isophthalic acid, 9 to 11 parts of 2, 2-bis (3, 5-difluoro-4-hydroxyphenyl) hexafluoropropane, 4.5 to 5.5 parts of N, N'-dihydroxypyromellitic diamine, 9 to 11 parts of 9, 9-bis [4-(4-methoxycarbonyl phenoxy) phenyl] fluorene and 1, 2-bis (4-(4-methoxycarbonyl phenoxy) phenyl] fluorene. The component A is prepared from 5.5 to 6.5 parts of 1, 4-cyclohexanedimethanol; the functional additive comprises an azobenzene derivative, a hot acid generator and a hydrogen bond enhancer; through the synergistic effect of a specific monomer combination, a functional additive and an optimization process, the technical bottleneck that heat resistance, transparency, dimensional stability and flexibility of an existing material are difficult to consider at the same time is broken through.

The invention discloses a method for preparing industrial hexane with ultralow benzene content through pre-hydrogenation. The method comprises the following steps: light naphtha, hydrogen and a hydrogenation catalyst are subjected to a hydrogenation reaction in a hydrogenation reactor for desulfurization and dearomatization, and a first mixture is obtained; feeding the first mixture into a gas-liquid separator to respectively obtain a liquid-phase product and a hydrogen-containing gas-phase product, and separating hydrogen from the gas-phase product through a circulating hydrogen compressor for recycling; and sequentially carrying out second rectification and third rectification on the liquid-phase product to obtain a heavy component substance, and adsorbing the heavy component substance through a molecular sieve. According to the method, by means of front hydrogenation reaction and rear molecular sieve adsorption, on one hand, the reaction load of molecular sieve adsorption is greatly reduced while the reaction activity of the hydrogenation reaction is improved; on the other hand, an extracting agent does not need to be added, other gas-phase and liquid-phase components are not introduced except hydrogen, the preparation process is greatly simplified, and the benzene content in the obtained cyclohexane is smaller than 5 ppm.

The invention relates to the technical field of waste polyester recycling and reusing, and discloses a method for depolymerizing copolyester, a depolymerization product and application of the depolymerization product in preparation of the copolyester. The preparation method comprises the following steps: carrying out a depolymerization reaction on copolyester with an average particle size of 0.1-5 cm to obtain a depolymerization solution containing bis (2-hydroxyethyl) terephthalate, a bis (2-hydroxyethyl) terephthalate dimer and cyclohexanedimethanol terephthalate; wherein the copolyester is polyethylene glycol terephthalate-1, 4-cyclohexanedimethanol ester, the water content in the copolyester is less than or equal to 2wt%, and the catalyst is a titanium-containing catalyst. According to the method disclosed by the invention, chemical depolymerization of PETG (or PCTG) copolyester can be realized, the depolymerization rate of the copolyester is improved, and a recyclable polymeric monomer is obtained.

This invention discloses a method for preparing polyethylene cyclohexanedicarboxylate (PECCHD) from waste PET. Specifically, it relates to a solvent composition for dissolving PET, characterized in that the solvent composition comprises a first solvent and a second solvent; the first solvent is a haloalcohol solvent or a cyclic ether solvent; the second solvent is one or more of a cyclic ether solvent, a chain ether solvent, a nitrile solvent, a ketone solvent, or a haloalkane solvent; the chain ether solvent is a chain ether solvent with 2-4 oxygen atoms; the volume ratio of the first solvent to the second solvent is 1:(1-5); the first solvent and the second solvent are not the same solvent. This method has significant advantages in terms of raw material adaptability, reaction efficiency, and industrialization potential, achieving a highly efficient conversion from low-end waste PET to high-value-added PECHD.

The invention provides a preparation method of a bamboo-based cellulose degradable plastic film containing modified PLA, and belongs to the technical field of plastic films. Bamboo-based cellulose is adopted as a biological matrix, PLA is adopted as a plastic matrix, firstly, 1, 2, 4-cyclohexanetriacetic anhydride is used for conducting prepolymerization treatment on the bamboo-based cellulose and the plastic matrix, interface bonding between the bamboo-based cellulose and the plastic matrix is enhanced, fluidity is improved, bamboo fibers are better wetted and wrapped by polymers, and entanglement and internal friction between the fibers are reduced. The PLA polymer and the DCP are mixed, under the synergistic effect of the DCP and the glycidyl methacrylate, a PLA polymer chain extends in a melt to form a thick protective layer, particle aggregation is prevented through the steric hindrance effect, a good dispersion effect is achieved in the melting process, and therefore the composite material with excellent mechanical performance and degradation performance is obtained.

The invention discloses a toluene hydrogenation catalyst used at room temperature and normal pressure as well as a preparation method and application thereof, oxidation modified carbon nanofibers are adopted as a carrier, and face-centered cubic Ru is loaded on the oxidation modified carbon nanofibers in the form of nanoparticles through solvothermal reaction to obtain the toluene hydrogenation catalyst. The catalyst provided by the invention can efficiently catalyze toluene hydrogenation to generate methylcyclohexane under the conditions of room temperature and normal hydrogen pressure. Compared with a traditional catalyst, the carbon oxide nanofiber supported ruthenium catalyst not only can work under relatively mild conditions, but also can keep relatively high activity in long-time use, and provides a key support for low cost of an organic liquid hydrogen storage technology.