1061 results about "Furan" patented technology

The invention discloses a large-current-carrying-capacity flexible power cable, which belongs to the technical field of cable preparation, is used for solving the technical problem that the flame retardant property and the mechanical property of the power cable need to be further improved in the prior art, and specifically comprises a cable core, a wrapping layer, an insulating layer and a sheath layer which are sequentially arranged from inside to outside. The preparation method comprises the following steps: preparing alkoxy silane containing a benzocyclobutene group, preparing flame-retardant particles by using a sol-gel method, preparing modified polyurethane by using modified polysiloxane and 2, 5-furandimethanol as soft segments, naphthalene diisocyanate as a hard segment and trimethylolpropane as a chain extender, and preparing the flame-retardant flame-retardant polyurethane. The linear low-density polyethylene, the MAH-g-PE, the modified polyurethane, the flame-retardant particles and the auxiliary additive are melted and extruded outside the wire core to form the insulating layer, so that the power cable is obtained, the flame-retardant property of the power cable is effectively improved, and the mechanical property and the current-carrying stability of the power cable are also improved.

The invention discloses a high-oxidation-resistance long-life polyethylene cable sheath material and a preparation method thereof, and relates to the technical field of high polymer materials. Comprising the following components: high-molecular-weight high-density polyethylene, surface-modified nano-dioxide, furan-maleimide grafted polyethylene, a Schiff base dynamic cross-linking agent, tea polyphenol grafted polyethylene, a temperature-responsive oxygen-blocking microcapsule, a main antioxidant, an auxiliary antioxidant, an emergency antioxidant, a light stabilizer, a halogen-free flame retardant, a processing aid and an acid absorbent. According to the invention, the main antioxidant, the auxiliary antioxidant and the tea polyphenol grafted polyethylene form a chemically synthesized and naturally modified composite antioxidant system, the designed service life of the material is greatly prolonged, the temperature-responsive oxygen-blocking microcapsule automatically cracks to release the core material when the operating temperature of the cable is greater than or equal to 90 DEG C, a dynamic oxygen-blocking layer is formed, and the service life of the cable is prolonged. The defect that the effect of traditional physical oxygen barrier is attenuated at high temperature is overcome, and the oxygen permeability at high temperature is reduced compared with that of a single nano barrier scheme.

The application provides a crosslinked polyethylene insulating material with intrinsic self-repairing and recyclable characteristics, a preparation method and application thereof, and relates to the technical field of cable materials.The crosslinked polyethylene insulating material with intrinsic self-repairing and recyclable characteristics is prepared from the following components in parts by weight: 99.7 parts by weight of low-density polyethylene, 1.0-2.6 parts by weight of peroxide, 0.1-0.5 parts by weight of antioxidant, 5-20 parts by weight of maleimide monomer, 0.35-0.7 parts by weight of catalyst, 0.5-3.0 parts by weight of ligand and 0.5-3.0 parts by weight of furan-based small molecule.The low-density polyethylene is functionally modified through catalytic amination reaction, so that the chain breaking and crosslinking in the modification process are avoided, and the mechanical properties, insulating properties and dielectric properties of the crosslinked polyethylene are enhanced through the post-absorption of the introduced peroxide.Meanwhile, the dynamic reversible Diels-Alder reaction introduced by the post-absorption of the furan-based small molecule enables the polyethylene insulating material to have good intrinsic self-repairing effect on mechanical damage and electrical damage.

The invention discloses a production method of a PET composite current collector base film with high mechanical property. The base film comprises an outer surface layer, a middle core layer and an inner surface layer, the outer surface layer is composed of PET, fumaric acid, hydroxyl-terminated polybutadiene and an antioxidant; the middle core layer consists of PET (Polyethylene Terephthalate), furandicarboxylic acid, an antioxidant and a stabilizer; the inner surface layer is composed of dimethyl terephthalate, ethylene glycol, spiro diol, ethylene glycol antimony and zinc acetate. The PET composite current collector base film prepared by the preparation method disclosed by the invention has relatively high mechanical properties.

The invention relates to the technical field of epoxy resin, in particular to self-repairing epoxy resin and a preparation method thereof. The self-repairing epoxy resin is prepared from the following raw materials in parts by mass: 80 to 120 parts of bisphenol A type epoxy resin, 20 to 40 parts of bisphenol F type epoxy resin, 5 to 15 parts of 1, 6-hexanediol diglycidyl ether, 1 to 3 parts of 3, 5-dimethylphenylboronic acid, 1 to 5 parts of furyl maleimide, 10 to 20 parts of dodecanedioic acid, 5 to 15 parts of butanetetracarboxylic acid, 1 to 3 parts of catalyst, 10 to 15 parts of nano silicon dioxide, 1 to 2 parts of boron nitride nanosheet and 1 to 2 parts of hyperbranched polyamidoamine. The curing agent is prepared from the following components in parts by weight: 20-30 parts of epoxy resin, 1-2 parts of sulfydryl-terminated polysiloxane, 20-30 parts of amine curing agent, 5-15 parts of reinforcing filler and 0.5 According to the invention, the balance among self-repairing capability, mechanical property and heat resistance is successfully realized; in the microcrack propagation process, fracture and recombination mechanisms of dynamic covalent bonds effectively prevent further propagation of cracks.

The invention discloses a DA bond polymer with antibacterial and self-repairing functions for a wood surface as well as a preparation method and a use method of the DA bond polymer. Chitosan serves as a wall material, cinnamon essential oil serves as a core material, the cinnamon essential oil and chitosan antibacterial microcapsules are prepared through emulsification, crosslinking and spray drying, and essential oil controlled release is achieved. Then bisphenol A diglycidyl ether DGEBA and furfuryl alcohol FA are used as raw materials, furyl functional epoxy resin FER is prepared under the catalysis of triethylamine TEA, bismaleimide BMI is added, and a DA bond self-repairing polymer is prepared through a DA reaction; and adding 4, 4-diaminodiphenylmethane DDM into the system, reacting with redundant DGEBA to generate a cross-linked polymer network, and adding the microcapsules into a DA bond semi-interpenetrating self-repairing network solution to obtain the DA bond polymer. A thin film formed by brushing and curing wood has antibacterial and self-repairing functions, scratches and microcracks on the surface of the wood can be repaired, and microbial erosion is inhibited.

The invention discloses a high-strength and high-resilience TPE (thermoplastic elastomer) and a preparation method thereof in the technical field of high polymer materials, and the elastomer is prepared by taking a hydrogenated styrene block copolymer as a matrix and matching with a polyolefin rigid phase, plasticizing oil and a specific additive. The method is characterized in that two self-made reaction type modifiers are introduced, wherein one self-made reaction type modifier is a core-shell nano reinforcing agent containing an epoxy functional group and polyhedral oligomeric siloxane, and the other self-made reaction type modifier is a furan maleimide bifunctional dynamic cross-linking agent. The nano reinforcing agent is prepared through silane hydrolysis and amination reaction, and can react with a matrix for grafting, so that the strength and creep resistance of the material are remarkably improved; the dynamic cross-linking agent is synthesized through step-by-step isocyanate addition reaction, a cross-linked network can be reversibly formed in the processing process, and the material is endowed with extremely high rebound resilience and low permanent deformation. The obtained product has high strength, high resilience and excellent processability, and is especially suitable for high-end fitness equipment.

The invention relates to polyethylene wax with a reversible crosslinking characteristic and a preparation method and application thereof, and relates to the field of polymer functional aids and processing and application thereof. The polyethylene wax with the reversible cross-linking characteristic is prepared from three monomers of furyl ethylene, maleimide ethylene and ethylene through double-bond addition copolymerization, and the number-average molecular weight is 1000-100000. The polyethylene wax provided by the invention can be used as a flow modifier during polyethylene material processing and a cross-linking modifier during use. The low molecular weight polyethylene wax can reduce the energy consumption of processing equipment and increase the flatness of the product. And meanwhile, the reversible crosslinking of furan and maleimide groups on the chain segment can endow the resin with thermoset property in use and thermoplastic cycle processability after use.

The synthesis method comprises the following steps: S1, adding furandicarboxylic acid into a reaction container, adding a certain amount of methanol, adding a double-acid-site strong acid solid catalyst, starting stirring, controlling the reaction temperature to carry out esterification reaction, and after the reaction is finished, filtering, washing and drying to obtain furandihydrazide; separating out the double-acid-site strong acid solid catalyst to obtain clear liquid, namely dimethyl furandicarboxylate; s2, transferring dimethyl furandicarboxylate serving as a raw material into another reaction container, adding a certain amount of sodium formate serving as a catalyst, then adding a proper amount of hydrazine hydrate, controlling the reaction temperature, keeping a reflux state, reacting for a period of time, cooling to room temperature after the reaction is finished, and performing centrifugal separation to obtain white solid furandihydrazide. The synthesis method has the advantages of simple reaction steps, no need of toxic and harmful catalysts, mild reaction conditions, high conversion rate and high yield, and can realize efficient, green and low-cost production of furandihydrazide.

The application discloses a furan resin composite material added with graphene and a preparation method thereof, and belongs to the technical field of furan resin composite material preparation. The preparation method of the furan resin composite material added with graphene comprises the following steps: step one, furan resin is added into a container, a curing agent is added during stirring, and continuous stirring is carried out to obtain a premixed resin; step two, a modified toughening agent is slowly added into the premixed resin, heating and continuous stirring are carried out to obtain a toughening mixture; step three, modified graphene is added into ethanol, ultrasonic dispersion is carried out, the toughening mixture is slowly dripped, high-speed stirring is carried out to obtain a composite mixture, the composite mixture is subjected to vacuum degassing, and then is added into a mold, solidification is carried out to obtain the furan resin composite material added with graphene. The composite material prepared by the method has excellent heat conductivity, flame retardancy and toughness.

The invention relates to a method for preparing high-molecular-weight polyethylene furandicarboxylate by a one-step method, and belongs to the technical field of bio-based polyester materials. The method comprises the following steps: weighing raw materials including 2, 5-furandicarboxylic acid, ethylene glycol, an end group regulator, a protective agent, a decarboxylation inhibitor and a catalyst, mixing and adding into a reaction container, introducing nitrogen, maintaining the pressure of the nitrogen in the reaction container to be 50-150 kPa, carrying out esterification reaction, heating and vacuumizing until the pressure is less than or equal to 50 Pa after the esterification reaction is completed, and carrying out polycondensation reaction to obtain the 2, 5-furandicarboxylic acid. And carrying out extrusion and drying so as to obtain the high-molecular-weight polyethylene furandicarboxylate, wherein the high-molecular-weight polyethylene furandicarboxylate is obtained. According to the method, the FDCA conversion rate is larger than or equal to 98%, the number-average molecular weight of the obtained product is larger than or equal to 32 kg / mol, no heavy metal residues exist, and the method is suitable for large-scale production of high-end bio-based packaging materials.

The invention discloses a hindered phenol monomer containing organic phosphorus heterocyclic rings as well as a preparation method and application of the hindered phenol monomer. The hindered phenol monomer has any one of the following structures: R is selected from-(CH2) b-or an aromatic ring, b is 3 or 4, and the aromatic ring comprises a benzene ring and / or a furan ring. The intrinsic flame-retardant anti-droplet polymer provided by the invention has the characteristics of excellent flame retardance and no droplet, and meanwhile, the intrinsic flame retardant is copolymerized into a molecular chain, so that the intrinsic flame-retardant anti-droplet polymer is not easy to migrate, does not permeate into the surrounding environment, is stable in property, can be used for injection molding and spinning, and can be used for preparing flame-retardant blocky products and fabrics; the composite material is used for interiors of electric appliances, switches, firefighter uniform, military uniform, automobiles, high-speed rails and other limited spaces.

An environmentally friendly fresh-keeping can and a method of manufacturing the same are provided. The environmentally friendly fresh-keeping can includes a housing, an inner container, an easy-open lid, and a bottom cover. The housing, the inner container, the easy-open lid, and the bottom cover are respectively made of a spiral paper tube, bio-based polyethylene 2,5-furanoate (PEF), aluminum, and biodegradable plastic. The inner container is mounted into the housing through an inner opening on a top of the inner container. Then the easy-open lid and the bottom cover are respectively used to seal the inner opening of the inner container and a bottom opening of the housing. The respective components are made of biodegradable, recyclable and reusable materials and able to be disassembled for recycling and reuse. Thereby the can meets requirements for environmental protection and recycling.

The invention provides a polyamide hot melt adhesive containing dynamic reversible covalent bonds and a preparation method thereof, and belongs to the field of high polymer materials. Caprolactam and nylon 66 salt are used as raw materials, a furan ring and a carbon chain with a specific length are introduced, and the polyamide hot melt adhesive containing the dynamic reversible covalent bond is obtained through polymerization with maleimide and a derivative thereof. The melting point of the polymer can be regulated and controlled by regulating and controlling the carbon chain length of aliphatic diamine introduced into the xF salt, a furan ring in the xF salt is subjected to DA addition reaction with maleimide and a derivative thereof, dynamic reversible sites are provided, crosslinking between molecular chains is formed, a net system is formed, and the bonding strength of the material can be greatly improved. By adjusting the ratio of the xF salt to the maleimide and the derivative thereof, the reversible crosslinking behavior of the polymer can be adjusted, and finally the hot melt adhesive which has a lower melting point and excellent bonding strength and can be repeatedly used and recycled is obtained.

The present invention relates to a dental diaphragm copolyester and a preparation method thereof, the preparation method comprises the following steps: 2, 5-furandicarboxylic acid or an ester thereof, aliphatic or alicyclic diol and (2-hydroxy-5-formyl phenyl) diphenylborane are subjected to a reaction to obtain an esterification or ester exchange product; and carrying out condensation polymerization on the esterification or ester exchange product and the stabilizer to prepare the copolyester for the dental diaphragm. 2, 5-furandicarboxylic acid is derived from a renewable biomass resource and meets the requirements of green and sustainable development; compared with terephthalic acid and furan ring structures, the film has higher rigidity and polarity, the yield of hot press molding is improved, the same correction force can be met by a thinner film, the wearing comfort of a patient is improved, and meanwhile stress relaxation is improved; the catalyst perfectly combines strong Lewis acidity, intramolecular stabilization and potential bifunctional activation through structural design, provides possibility for efficient and green synthesis of polyester, avoids use of heavy metal, and is higher in biological safety.

The invention discloses SIS (styrene-isoprene-styrene) containing dynamic reversible bonds and a preparation method thereof, and belongs to the technical field of high polymer materials. The copolymer is prepared through a Diels-Alder reaction with bismaleimide on the basis of a polystyrene construction unit with two tail ends capped with furan and a polyisoprene construction unit module with two tail ends capped with furan. Wherein the DA bond has a thermal reversible characteristic. The furan end-capped building unit module with controllable molecular weight and narrow distribution is prepared, and reversible connection and dissociation of blocks are realized through a modularization strategy. According to the invention, an inverse Diels-Alder reaction can be carried out at 120-140 DEG C, and is dissociated into an original construction unit module, so that the proportion of soft and hard segments of a copolymer is changed by supplementing a specific construction unit feeding amount and carrying out the Diels-Alder reaction again; the SIS has the advantages of being accurate in structure and designable in performance at the same time, flexible regulation and control over the block proportion are achieved through the SIS containing the dynamic reversible bonds, and meanwhile the SIS has wide application prospects in the fields of recyclable adhesives, intelligent packaging, flexible electronics and the like.

The invention discloses polycaprolactone dihydric alcohol containing maleimide groups and a preparation method and application thereof, and the preparation method of the polycaprolactone dihydric alcohol comprises the following steps: adding N-(2, 3-dihydroxy propyl) maleimide, caprolactone and a catalyst into a reaction container, carrying out high-temperature reaction for 12-18 hours, filtering, washing, and drying to obtain the polycaprolactone dihydric alcohol containing the maleimide groups. And cooling and discharging to obtain the polycaprolactone diol containing the maleimide group. The polycaprolactone diol containing the maleimide group is used as a raw material to prepare a polyurethane prepolymer, so that the side chain of the prepolymer is provided with the maleimide group, and then a difuran compound is introduced as a dynamic cross-linking agent to obtain the self-repairing polyurethane elastomer containing the Diels-Alder bond. Through the reversible Diels-Alder (D-A) reaction effect of the functional components, the polyurethane elastomer can be remodeled and recycled, and the polyurethane elastomer has excellent and stable mechanical properties, self-repairing efficiency and repeated self-repairing capability.

The invention relates to the field of polyimide films, and discloses a catalytic polyimide film with a low thermal expansion coefficient and a preparation method thereof, the catalytic polyimide film comprises 43-47% of a rigid polyimide material, 28-32% of a flexible polyimide material, 4-6% of a dynamic cross-linking agent, 7-9% of a component agent, and the balance of a solvent; the dynamic cross-linking agent comprises maleimide terminated polyamide and a difuran compound, and the ratio of the maleimide terminated polyamide to the difuran compound is 3: 2. Through the synergistic effect of constructing a stable framework by a rigid polyimide material, buffering stress by a flexible polyimide material and uniformly dissipating heat by flaky boron nitride, a chemical regulation and control system of'rigid constraint-flexible buffering-heat conduction balance 'is formed, thermal expansion is inhibited from the molecular level, and compared with a traditional physical method which purely depends on external force or a single component, the thermal expansion coefficient is greatly improved. According to the system, through complementation of chemical mechanisms of all components, the dimensional stability under temperature fluctuation is improved to a new height, and the problem that the thermal expansion coefficient in a wide temperature range is difficult to control is solved.

A method of preparing 2-hydroxyadpic acid and adipic acid is provided. The method of preparing 2-hydroxyadpic acid and adipic acid comprises a step of the electrolysis of 2,5-furandicarboxylic acid using a metal electrode at a constant current in a sulfuric acid solution containing a quaternary ammonium salt. The metal electrode is a bismuth electrode or a lead electrode. The quaternary ammonium salt is represented by formula (I):wherein R1 to R4 are independently a C2-5 hydrocarbon group, and X− is ClO4−, H2PO4−, or Br−.

The invention belongs to a preparation method of furan resin, and provides formaldehyde-free plant polyphenol modified furan resin and a preparation method thereof in order to solve the technical problems of formaldehyde harm, non-renewable raw material phenol source and poor environmental protection property in the existing furan resin preparation process. The plant polyphenol modified furan resin is prepared by carrying out condensation polymerization on a phenolic mixture and bio-based aldehydes, and the phenolic mixture comprises plant polyphenol and another phenolic compound. The crosslinking density and the mechanical property of the resin are obviously improved. Meanwhile, a three-dimensional cross-linked network is constructed by replacing formaldehyde with a bio-based aldehyde compound to serve as a cross-linking agent, and mild and controllable reaction conditions are realized by combining a weakly acidic environment-friendly catalyst system. The problem of formaldehyde release in the resin synthesis and curing process is effectively solved, the obtained resin is high in bio-based content, has the rapid curing characteristic and excellent mechanical strength, the wastewater treatment difficulty is remarkably reduced, and the remarkable environment-friendly advantage is achieved.

The invention discloses a hydrolysis-resistant bio-based polyester polyol modified waterborne polyurethane adhesive, belongs to the technical field of adhesive preparation, and is used for solving the technical problem that the hydrolysis resistance and the adhesive property of a waterborne polyurethane adhesive in the prior art need to be further improved. Furan carbonate-polyester polyol is used as a matrix, phosphorus-silicon cross-linked flame-retardant polyol and a modified curing agent are used as auxiliary materials to construct a multi-layer cross-linked structure, a furan carbonate unit is introduced into a main chain to improve the rigidity and polarity matching of a molecular chain, and an organic-inorganic stable network is formed by using the phosphorus-silicon cross-linked structure; according to the preparation method, the polyurethane is taken as a raw material, and post-crosslinking densification is realized through the modified curing agent, so that chain segment migration and hydrolysis reaction are effectively inhibited, the interface bonding stability and thermal oxidation tolerance are improved, and the prepared polyurethane adhesive has high shear strength, excellent flame retardance and excellent damp-heat aging retention rate and balanced and stable performance at the same time.

The invention relates to a double-self-repairing hydroxyl acrylic coating and a spraying process thereof, and belongs to the technical field of coatings. Comprising 50 to 60 parts of a hydroxy acrylic resin-furan modified copolymer, 5 to 10 parts of a maleimide compound, 3 to 8 parts of propylene glycol methyl ether acetate, 5 to 10 parts of dimethyl carbonate, 5 to 8 parts of polyurethane microcapsules, 5 to 7 parts of carbon black, 2 to 5 parts of modified titanium dioxide, 0.8 to 1.2 parts of a modified polyether siloxane leveling agent and 0.2 to 0.4 part of an organic bismuth-zinc composite drier. 2 to 5 parts of fumed silica; and 1 to 2 parts of nano montmorillonite. The paint provided by the invention can form a uniform and continuous coating on the surface of a base material. When the coating is damaged by scratches and the like, self-repairing can be achieved through double mechanisms. According to the spraying process, the polyurethane microcapsules and the matrix resin are separately mixed, and breakage caused by direct mixing of the microcapsules and the resin can be effectively avoided.

The invention relates to a cross-scale thermal response self-repairing polyurethane material as well as a preparation method and application thereof, and belongs to the field of self-repairing polyurethane materials. A pyridine group is introduced into a main chain of the polyurethane material to form a reversible coordination bond with metal salt, so that molecular-scale self-repairing is realized, and the dynamic property of the coordination bond can be enhanced by a preferable double-metal synergistic system; a side chain is designed to be of a furan-maleimide structure based on a Diels-Alder reaction, thermal response macroscopic self-repairing performance is given to the material, a methyl substituted furan group is introduced to improve steric hindrance, and the high-temperature application scene can be expanded. The polyurethane material has a thermal response and metal coordination dual self-repairing mechanism, and is suitable for polymer protection and repairing application under severe working conditions of high temperature, high ion concentration and the like.

The invention belongs to the technical field of natural medicines, and particularly relates to application of spermidine alkaloid in preparation of anti-tumor medicines and / or reversion of drug resistance. The invention provides an application of macrocyclic spermidine alkaloid in preparation of anti-tumor drugs and / or reverse drug resistance. The macrocyclic spermidine alkaloid comprises one or more than two of 13-oxo-furan celastrus orbiculatus, furan celastrus orbiculatus, benzene-substituted celastrus orbiculatus and celastrus orbiculatus cinnamamide alkali. The macrocyclic spermidine alkaloid disclosed by the invention has the characteristics of broad-spectrum anti-tumor effect, good anti-tumor effect, relatively low toxic and side effects, capability of reversing 5-fluorouracil drug resistance, relatively high water solubility, relatively easy source, simple structure, only one chiral carbon in the structure, relatively easy artificial synthesis, intervention in cell autophagy mechanism and the like, so that the overall treatment cost is relatively low; the method has a potential important clinical application prospect.

The invention discloses a tetrahydrocarbazole enhanced fluorescent probe for detecting hydrosulfite as well as a preparation method and application of the tetrahydrocarbazole enhanced fluorescent probe. The fluorescent probe is a 2-(2-(5-(2, 2-dimethyl-2, 3, 4, 9-tetrahydro-1H-1, 3-methyl carbazole-6-yl) furan-2-yl) vinyl)-3-ethyl benzothiazole-3-onium iodised salt compound, namely, TC-FV-BT, and the fluorescent probe can be applied to the field of fluorescence detection. The probe TC-FV-BT can be used for specifically recognizing the hydrosulfite. Under sunlight, after bisulfite is added into a DMF / H2O (2: 8, v / v) solution of the probe TC-FV-BT, the color of the solution is changed from dark pink to white, under irradiation of ultraviolet light with the wavelength of 365 nm, the solution emits orange fluorescence at the emission wavelength of 605 nm, the fluorescence color of the solution is changed from colorless to orange, the response time is 4 min, the detection limit of the bisulfite reaches 77.27 nM, and the detection limit of the bisulfite reaches 77.27 nM. The fluorescent probe shows good selectivity and anti-interference performance, and has a good application prospect in the fields of environmental analysis, food and the like as a fluorescent probe for detecting hydrosulfite.

The present disclosure provides a hydrogel composition for tissue engineering and regenerative medicine, including naturally derived polymers functionalized with furan groups and nanoparticles of poly(lactic-co-glycolic acid)-poly(ethylene glycol) copolymer functionalized with maleimide groups. Covalent crosslinking via a bioorthogonal Diels-Alder click reaction forms a tunable, biocompatible, and biodegradable three-dimensional network. The hydrogel composition mimics the extracellular matrix and offers adjustable mechanical properties, controlled biodegradation, and therapeutic agent delivery for applications such as cartilage regeneration and drug delivery.

This invention proposes a catalyst component, catalyst, and their applications for olefin polymerization, belonging to the field of olefin polymerization technology. The catalyst component contains products obtained from the reaction of a magnesium source, a titanium source, and an internal electron donor, wherein the internal electron donor comprises furan compounds and diether compounds. The catalyst of this invention exhibits high hydrogen sensitivity and stereoregulation, with a good balance between the two. The molecular weight distribution of the prepared low melt index polymer is broader than that of the high melt index polymer, and the catalyst component of this invention does not contain phthalate compounds (plasticizers).

The invention relates to the technical field of chemical synthesis, and discloses a method for preparing 2, 5-furandicarboxylic acid, which comprises the following steps: dispersing cobalt nitrate and nickel sulfate into an aqueous solution of polyvinylpyrrolidone at room temperature; adding a sodium borohydride solution to obtain nano colloid; preparing an aqueous suspension of cerium oxide, and adding the aqueous suspension into the nano colloid; centrifugally filtering, and recovering a solid product; washing the solid product; centrifuging, putting solid powder obtained after centrifuging into a drying oven, and drying; and calcining and grinding the solid powder to finally prepare the Co-Ni / CeO2 catalyst. And dissolving 5-hydroxymethylfurfural in water at normal temperature, adding the prepared Co-Ni / CeO2 catalyst and a sodium hypochlorite solution, reacting, and filtering to remove the catalyst, thereby obtaining the 2, 5-furandicarboxylic acid. The method disclosed by the invention has the advantages of no use of strong base, low reaction temperature, short reaction time, few byproducts, greenness and sustainability.

The invention belongs to the technical field of fermentation engineering, and particularly relates to a staphylococcus pseudoxylosus strain and application of the staphylococcus pseudoxylosus strain in enhancing the flavor of fermented food, and the preservation number of the staphylococcus pseudoxylosus strain is GDMCC NO: 66815. The strain can produce lipase and protease, and can significantly enhance the content of flavor substances such as ketones, alcohols, esters, pyrazine furans and the like in fermented food. And inoculating the staphylococcus pseudoxylosus E2 into food to be fermented, and fermenting at 25-40 DEG C for 5-35 days. Compared with natural fermentation, the content of flavor substances in fermented food can be remarkably increased, and the method is suitable for commercialization.