8228 results about "Cross linker" patented technology

The invention discloses a repulpable and degradable PHA heat-seal barrier coating and a composition thereof, and belongs to the field of water-based functional coatings and cellulose-based packaging materials. The coating composition is prepared from the following components in percentage by non-volatile solids: 30 to 85 weight percent of polyhydroxyalkanoate emulsion, 5 to 60 weight percent of flaky natural inorganic matters, a water-based cross-linking agent and an auxiliary agent, and 1 to 20 weight percent of ethylene-acrylic acid or ethylene-methyl acrylate dispersion can be selected. The pH value of the composition is 6.5-9.0, and organic fluorine is not artificially added. When the dry weight is 6-20 g / m, the coating meets at least one of the following four items: the water vapor transmission rate (38 DEG C, 90% RH) is less than or equal to 80 g / m.d, Cobb60 is less than or equal to 15 g / m, the oil resistance grade is greater than or equal to 11, and the laboratory repulping rate is greater than or equal to 98%; and the heat-sealing peel strength is greater than or equal to 2.5 N / 15mm under the conditions of 150 DEG C, 0.2 MPa and 0.5 s. And the coating and the stripping film thereof meet the industrial composting standard.

The invention belongs to the technical field of solid-state lithium batteries, and relates to a fluorinated double-salt cross-linked solid-state electrolyte adaptive to a lithium-free negative electrode, a solid-state lithium battery and a preparation method thereof.The preparation method comprises the steps that double-lithium salt is dissolved in a fluorinated solvent to obtain an electrolyte, then a monomer, a cross-linking agent and an initiator are added, the mixture is stirred to be uniform to obtain a precursor solution, and the precursor solution is prepared; and assembling the precursor solution, a positive electrode, a negative electrode and a solid-state electrolyte composite diaphragm into a battery, and performing gradient polymerization to form the solid-state lithium battery. According to the invention, the ionic conductivity of the solid electrolyte is more than 5 * 10 <-4 > S / cm and the oxidation potential of the solid electrolyte is more than 5.8 V by adopting a fluorinated solvent consisting of fluorinated carbonate and fluorinated carboxylate and a double-lithium-salt synergistic system and combining an in-situ interface fusion technology, so that the solid electrolyte can be matched with a 4.8 V high-voltage lithium-rich manganese-based positive electrode and a lithium-free negative electrode; and the energy density and the safety of the solid-state lithium battery are improved. The electrolyte scheme is low in cost, high in safety and good in positive and negative electrode matching performance, can be compatible with an existing battery production line, and is convenient for large-scale production.

The invention relates to a composite solid electrolyte membrane with high ceramic content and a preparation method and application thereof. The preparation method comprises the following steps: mixing ceramic solid electrolyte particles activated by a silane coupling agent with an in-situ polymerization solution containing a cross-linking agent, an organic monomer, a plasticizer, a lithium salt, an ultraviolet light initiator and a thermal initiator to form solid electrolyte slurry, wherein the ceramic solid electrolyte particles account for 60-90% of the total mass of the composite solid electrolyte membrane; the preparation method comprises the following steps: coating a positive pole piece with solid electrolyte slurry, initiating shallow organic matter monomers and a cross-linking agent to generate in-situ polymerization through an ultraviolet light initiator, covering a negative pole piece for hot pressing treatment, initiating residual organic matter monomers and the cross-linking agent to generate in-situ polymerization through a thermal initiator, and forming a composite electrolyte membrane with high ceramic content. The invention also discloses an all-solid-state battery containing the composite solid electrolyte membrane. The solid-state battery containing the in-situ formed composite solid-state electrolyte membrane has relatively high cycling stability.

The invention discloses a transparent composition photoresist with low shrinkage and low vacuum deflation. Comprising the following raw materials in percentage by mass: 1-5% of modified polyhedral oligomeric silsesquioxane (POSS), 1-5% of an expanding monomer, 1-5% of modified acrylic resin, 1-5% of epoxy resin, 1-5% of a thiol cross-linking agent, 1-5% of an initiator, 0.1-3% of a curing accelerator, 0.2-0.5% of a flatting agent, 0.1-5% of a silane coupling agent, 0.01-0.2% of an antioxidant and 80-90% of an electronic-grade organic solvent. The invention also provides a preparation method of a cured coating prepared from the transparent composition photoresist with low shrinkage and low vacuum deflation. The product provided by the invention not only can maintain the properties of high hardness, high thermal stability, high planarization ability, high barrier property, low hygroscopicity, low dielectric constant and the like of the transparent composition photoresist coating, but also can enable the transparent composition photoresist coating to have excellent low shrinkage and low outgassing, thereby achieving the purposes of saving energy, reducing emission, reducing cost and improving efficiency; the low shrinkage of the transparent composition photoresist coating also widens the development of the material in the fields of other panel production processes such as OLED (Organic Light Emitting Diode) and the like.

The invention discloses a large-size green packaging carton and a preparation process thereof, and relates to the field of packaging box preparation. The environment-friendly composite material comprises the following raw materials in parts by weight: 50-80 parts of plant fiber slurry, 10-25 parts of a modified starch-based adhesive, 5-15 parts of a nanoscale inorganic reinforcing filler, 1-5 parts of a degradable water repellent agent, 0.5-3 parts of a cross-linking agent and 2-8 parts of starch and plant fiber composite buffer microspheres. According to the preparation method, full-environment-friendly raw materials such as plant fiber slurry and a modified starch-based adhesive are selected and matched with starch and plant fiber composite buffer microspheres, and optimized processes such as segmented temperature control pressurization molding, adhesive gelatinization treatment, stirring speed reduction and microsphere structure protection are combined; and through coating of the degradable polymer coating and micron-sized hydrophobic texture imprinting, synergistic improvement of high compressive strength, excellent buffering performance, excellent hydrophobic and damp-proof effects and high degradation rate of the carton is achieved.

The invention discloses an anti-shrinkage light, soft and elastic sole foaming material and a preparation method thereof, and belongs to the technical field of footwear products. The light, soft and elastic sole foaming material is formed by chemically foaming an EVA (Ethylene Vinyl Acetate) composite raw material, the EVA composite raw material is prepared from 50 to 70 parts of EVA, 20 to 40 parts of olefin thermoplastic elastomer, 10 to 20 parts of styrene elastomer, 1.5 to 3 parts of maleic anhydride grafted ethylene-octylene copolymer compatilizer, 0.4 to 0.8 part of peroxide cross-linking agent, 3 to 4 parts of foaming agent, 1 to 1.5 parts of zinc oxide, 1 to 1.5 parts of polyethylene wax substance and 0.5 to 1.5 parts of poly (butylene succinate). 0.3 to 1 part of polyamide 12 microspheres and 2 to 3 parts of nano montmorillonite. The foaming material can resist shrinkage when being used as a shoe sole part, and has good rebound performance and the like, so that the high-quality requirement of sneakers, the mass production stability and the like are met.

The invention belongs to the technical field of lithium ion batteries, and particularly relates to a self-repairing type lithium ion battery positive electrode adhesive, a preparation method, positive electrode slurry and a positive electrode plate. The adhesive comprises a mixed solvent, and a first copolymer serving as a main component and a second copolymer serving as a cross-linking agent are dissolved in the mixed solvent; the first copolymer is an acrylate-based multipolymer containing carboxyl or hydroxyl; the second copolymer is isocyanate terminated UPy functional polyurethane; the adhesive is in a liquid state at room temperature, when the adhesive is subjected to vacuum heat treatment at 60-180 DEG C, carboxyl or hydroxyl in main components of the adhesive reacts with isocyanate groups of a cross-linking agent to form amido bonds along with volatilization of a mixed solvent, and UPy groups are associated through quadruple hydrogen bonds to form dual dynamic cross-linking points. The method can effectively adapt to the volume change of the positive electrode material in the lithium removal / insertion process, and maintains the integrity of the electrode structure, thereby improving the cycling stability and rate capability of the lithium ion battery.

The invention provides a low-smoke halogen-free flame-retardant cable material and a preparation method thereof, and belongs to the field of cable materials. The low-smoke halogen-free flame-retardant cable material is prepared from the following chemical components: 32 to 40 parts of nitrile rubber, 22 to 27 parts of natural rubber, 8 to 12 parts of benzoxazole-siloxane copolymer containing phosphate dynamic bonds, 13 to 15 parts of core-shell-sheath three-stage structure flame retardant, 4 to 6 parts of hexaphenoxy cyclotriphosphazene modified carbon nanotubes, 2 to 3 parts of europium-doped mesoporous cerium dioxide and 3 to 4 parts of nano zinc oxide. The composite material is prepared from the following components in parts by weight: 3 to 4 parts of carbon nanotube grafted montmorillonite hybrid, 2 to 3 parts of lubricant, 0.8 to 1.2 parts of cross-linking agent, 0.3 to 0.4 part of accelerant, 0.4 to 0.6 part of dicumyl peroxide and 0.1 to 0.2 part of antioxidant. Unification of high flame retardance, low smoke, excellent mechanical property and processability of the cable material is realized.

The invention relates to double-layer integrated asymmetric viscous hydrogel as well as a preparation method and application thereof, and belongs to the technical field of hydrogel. The invention relates to a preparation method of double-layer integrated asymmetric viscous hydrogel, which comprises the following steps: adding natural macromolecular polysaccharide and a polymeric monomer into a salt solution, stirring at room temperature, then adding an initiator and a cross-linking agent, stirring and polymerizing to obtain the double-layer integrated asymmetric viscous hydrogel. Through a one-pot method, a salt component is introduced into a hydrogel system, and the hydrogel has a double-layer structure with asymmetric viscosity under the salting-out action; in addition, the hydrogel is doped with a carbon nanotube with the surface modified by polydopamine and silver nanoparticles, so that the mechanical property and the conductivity of the hydrogel are remarkably improved. The preparation method provided by the invention is simple, is suitable for various hydrogel systems, has good universality and is easy to popularize and apply.

The invention provides a thermal interface material based on vinyl imidazole ionic liquid as well as a preparation method and application of the thermal interface material. The thermal interface material is prepared from the following raw materials: the vinyl imidazole ionic liquid, a heat-conducting filler subjected to surface treatment by a silane coupling agent, an initiator and a cross-linking agent. The thermal interface material is based on the vinyl imidazole ionic liquid and the heat-conducting filler, the limitation of a traditional thermal interface material base body is broken through, dispensing can be achieved, no solvent is needed in the preparation process, the adverse effect of solvent residues on the performance of a chip when the thermal interface material is applied to the chip subsequently can be avoided, and the thermal interface material has ideal interface bonding strength; the heat conduction effect is remarkable and stable, the heat stability is good, the material can be well attached to an interface, the problems of stress concentration, cracks and the like are not prone to occurring, and the material can be widely applied to the heat conduction and heat dissipation fields of aerospace, advanced energy, electronic information, military industry and the like.

The invention discloses a dry-process high-temperature-resistant lithium battery diaphragm and a preparation method thereof, and relates to the technical field of lithium battery diaphragms. The specific preparation method comprises the following steps: activating and cross-linking polypropylene, polyimide, a PP-b-PI block copolymer and a cross-linking agent BIBP under the protection of nitrogen to prepare a polypropylene-polyimide matrix; after melting, adding a pre-sintered ZrO2-coated Al2O3 core-shell filler, hydroxylated boron nitride and zinc borate, and carrying out double-stage screw extrusion, ultrasonic orientation, nitrogen annealing and cold roller quenching to obtain a mixed melt; carrying out warm stretching and hot air circulation heat treatment to prepare a hard elastic crystal base film; carrying out stretching, thermal relaxation and thermal shaping to obtain a microporous base membrane; after slitting, plasma activation is carried out, epoxy silane and tetraethyl orthosilicate / polybenzimidazole aerogel precursors are sprayed, and a nano closed-pore coating is formed through pre-curing and heat shrinkage curing; and finally eliminating static electricity and rolling to obtain a finished product. The lithium battery diaphragm prepared by the invention is excellent in high temperature resistance and low in thermal shrinkage rate.

The invention relates to a composite solid electrolyte and a preparation method and application thereof. The preparation method of the composite solid electrolyte comprises the following steps: S1, mixing an inorganic filler and a fluorine-containing compound, and reacting at 70-90 DEG C under an acidic condition to obtain an inorganic filler wrapped by a fluorinated layer; then adding a fluorine ion complexing agent and a silane coupling agent for reaction to obtain a modified filler; adding a thermal decomposition type cross-linking agent into the polymer, and carrying out melt blending to obtain a cross-linked polymer; s2, uniformly mixing the modified filler, a cross-linked polymer, a lithium salt and a solvent to obtain a plurality of slurries containing the modified filler with different volume concentrations; and molding the slurry to prepare the composite solid electrolyte. According to the method, the fluorinated layer and the siloxane network are constructed step by step, so that the interface impedance is reduced, and efficient dissociation of the lithium salt is promoted; a three-dimensional network structure is combined, so that the tensile strength is improved; the modified filler is further designed in a gradient manner to improve the lithium ion transference number.

The invention discloses forest steppe fire extinguishing barrier foam and a preparation method thereof.The foam is prepared from 5%-20% of a material A, 0.5%-0.8% of a material B, 1.8%-3% of a coagulant and the balance water through a foam generation system; the material A is prepared from 1 to 10 parts of organic aggregate and 100 to 200 parts of inorganic aggregate; the material B is composed of 2-7 parts of a composite surfactant and 1-6 parts of a cross-linking agent; the coagulant is carbon dioxide gas. The inorganic aggregate is condensed under the action of hydrogen ions generated by dissolution of carbon dioxide to form colloidal particles, the colloidal particles are polymerized and crosslinked with the organic aggregate to form a gel skeleton of a three-dimensional network structure, the foam is converted into gel foam, and a heat-insulating and anti-burning barrier layer is formed on the surface of a combustible. The fire extinguishing agent is high in fire extinguishing efficiency, good in heat insulation effect and environment-friendly, and has wide application prospects in forest and grassland fire disasters.

The invention relates to the technical field of plastic material preparation, and discloses a modified bamboo fiber, a PBAT composite material and a plastic object. The modified bamboo fiber comprises bamboo fiber subjected to hot pressing treatment in water and a closed aziridine cross-linking agent loaded on the bamboo fiber, and the mass ratio of the bamboo fiber subjected to hot pressing treatment in water to the closed aziridine cross-linking agent is 100: (1-10). The PBAT composite material comprises the following components in parts by weight: PBAT and modified bamboo fibers, and the mass ratio of the PBAT to the modified bamboo fibers is 100: (20-40). The modified bamboo fiber is subjected to hot pressing treatment in water, so that the generation of volatile gas caused by high-temperature processing can be avoided when the modified bamboo fiber is applied to the plastic material, and the interface interaction with the plastic material can be improved; the closed aziridine cross-linking agent can release active groups at high temperature, and can react with active functional groups such as hydroxyl and carboxyl on the surfaces of the bamboo fibers and the surfaces of the plastic materials, so that the interface interaction between the bamboo fibers and the plastic matrix is improved, and the tensile strength of the composite material is improved.

The invention discloses a light-moisture dual-curing underwater epoxy coating with a self-repairing function as well as a preparation method and a construction method of the light-moisture dual-curing underwater epoxy coating. The epoxy coating comprises a component A and a component B, wherein the mass ratio of the component A to the component B is (1.5-3.5): 1; the component A is prepared from the following raw materials: bisphenol F type epoxy resin, dynamic disulfide bond modified polysulfide rubber, boron nitride nanosheet and silicon carbide nanowire hybrid filler, a photoinitiator and a silane coupling agent; the component B is prepared from the following raw materials: moisture-cured polyether amine, a boric acid ester bond cross-linking agent and hydrophobic modified graphene oxide. According to the invention, a light-moisture dual-curing mechanism is adopted, ultraviolet irradiation initiates rapid surface curing, and then environmental moisture permeates to complete deep curing. The material provided by the invention has the advantages of rapid curing, excellent self-repairing function, significantly improved underwater adhesion and good thermal conductivity, and provides a new solution for rapid repairing and long-acting protection of underwater structures.

The invention provides a high-hydrophobicity anti-pollution flashover coating and a preparation method thereof, and relates to the field of coatings. The silicone rubber composition is prepared from the following raw materials in parts by weight: 80 to 100 parts of hydroxyl-terminated polydimethylsiloxane; 5 to 15 parts of modified nano silicon dioxide; 10 to 30 parts of a composite self-repairing microcapsule; 10 to 25 parts of a flame retardant; 3-8 parts of a cross-linking agent; 0.5-2 parts of a catalyst; 1-5 parts of an accelerant; 40 to 100 parts of a solvent; the modified nano silicon dioxide is fumed silica subjected to surface treatment by a fluorine-containing silane coupling agent and a platinum catalyst; the capsule wall of the composite self-repairing microcapsule is a polylactic acid-glycolic acid copolymer, and the capsule core of the composite self-repairing microcapsule is a mixed solution of a hydroxyl-terminated polydimethylsiloxane oligomer and methyltris (methylethylketoximino) silane. The coating has excellent hydrophobicity, weather resistance and targeted repair function.

The invention discloses a composite polyacrylamide flocculant based on a nano core-shell structure as well as a preparation method and application of the composite polyacrylamide flocculant. The composite polyacrylamide flocculant is a core-shell structure composite material which takes inorganic nanoparticles grafted with carbon-carbon double bonds on the surface as a core and takes a polyacrylamide copolymer as a shell; the polyacrylamide copolymer is prepared from the following components in parts by mass: 70 to 90 parts of acrylamide, 10 to 30 parts of functional monomer and 0.1 to 1.0 part of cross-linking agent. The basic conception of the flocculating agent provided by the invention is that the structural design of inorganic nano core-organic polymer shell is adopted, PAM molecular chains firmly grow on the surfaces of nano particles in a chemical grafting manner, high dispersion and functional synergy of nano units are realized, and the obtained product has the characteristics of high flocculation speed, dense floc, high removal efficiency and the like, and has a wide application prospect. The method is especially suitable for deep treatment of difficult-to-treat industrial wastewater such as oil-containing wastewater, dye wastewater and heavy metal wastewater.

The invention relates to the technical field of sodium-ion batteries, and discloses a super-crosslinked asphalt-based hard carbon material, a preparation method and application thereof, and a sodium-ion battery. Asphalt is subjected to super-crosslinking by adopting a mechanochemical method, and the asphalt, a crosslinking agent and a catalyst realize fracture and recombination of chemical bonds under the action of mechanical shearing force of grinding balls, so that the super-crosslinked asphalt-based hard carbon material is obtained. According to the present invention, the asphalt is subjected to segmented ball milling and super-crosslinking, and then carbonization sintering is performed, such that the asphalt cannot be subjected to molecular rearrangement so as to finally form the hard carbon material with the more suitable microporous structure and the more suitable interlayer spacing, such that the negative electrode ion embedding requirement of the sodium ion battery is met, the excellent sodium storage performance is represented, and the capacity and the first coulombic efficiency of the assembled battery are improved; the performance improvement of the sodium ion battery is integrally promoted. The method is low in energy consumption, short in time consumption, simple in parameter control and suitable for large-scale application and popularization.

The invention provides an adsorbent capable of simultaneously adsorbing bilirubin and cytokines and a preparation method and application thereof, and the preparation method comprises the following steps: carrying out suspension polymerization reaction on a styrene monomer and a polyvinyl cross-linking agent in a dispersion medium under the action of a continuous multi-component pore-foaming agent and an initiator to prepare polystyrene-based macroporous resin; carrying out chloromethylation reaction on the polystyrene-based macroporous resin to prepare chlorine balls; carrying out post-crosslinking reaction on the chloromethylated beads to prepare the adsorbent capable of adsorbing bilirubin and cytokines at the same time; the continuous multi-component pore-foaming agent comprises a first pore-foaming agent, a second pore-foaming agent and a third pore-foaming agent of which the solubility parameters are gradually increased in sequence; the temperature of the suspension polymerization reaction is adjusted according to the mass fraction of the polyvinyl cross-linking agent in the monomer mixture and the solubility parameter of the continuous multi-component pore-foaming agent, and the monomer mixture is composed of styrene monomers and the polyvinyl cross-linking agent. The bilirubin and cell factors can be adsorbed at the same time, and the safety of blood purification is improved.

The invention discloses a method for synthesizing electronic-grade ethyl acetate through catalytic esterification of acidic ion exchange resin, and belongs to the technical field of ethyl acetate preparation. The method comprises the following steps: mixing crosslinked polystyrene white balls and a swelling agent, and dropwise adding concentrated sulfuric acid for reaction to obtain S-PS resin; mixing an EDTA disodium salt saturated solution and a polyacrylic acid solution, adding a cross-linking agent and an emulsifier, and carrying out a cross-linking curing reaction to obtain EDTA microcapsules; the preparation method comprises the following steps: dispersing S-PS resin in a solvent, adding EDTA microcapsules, a dehydration condensation agent and a catalyst, reacting under the protection of inert gas, and filtering and recovering after the reaction is finished to obtain S-PS-EDTA resin; mixing glacial acetic acid, absolute ethyl alcohol and S-PS (at) EDTA resin for reaction, and filtering and collecting liquid after the reaction is finished; and rectifying the collected liquid to obtain the product. According to the method provided by the invention, metal impurities can be chelated in the synthesis process, and the electronic-grade ethyl acetate with high purity and low impurity content is produced.

The invention relates to the field of packaging materials, and discloses low-temperature heat-sealing water-based coated paper and a preparation method and application thereof.The water-based coated paper comprises a base paper layer and a water-based coating, and the water-based coating comprises water-based ethylene-acrylic acid copolymer emulsion, modified nano-silica, a coalescing agent and water; a cardanol derivative is introduced into the water-based ethylene-acrylic acid copolymer emulsion as a functional component; the cardanol derivative is prepared by reacting epoxidized cardanol with 9, 10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide and then grafting with acryloyl chloride. The preparation method comprises the following steps: reacting epoxidized cardanol with 9, 10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide; the modified nano silicon dioxide is prepared by mixing aminated nano silicon dioxide and chitosan and adding a cross-linking agent prepared by grafting phytic acid and ethylene glycol diglycidyl ether. The water-based coating paper prepared by the invention overcomes the defects that the existing BOPP film is not environment-friendly, and the conventional coating paper is high in heat sealing temperature and easy to stick; meanwhile, good mechanical properties, water resistance and flame retardance are achieved.

The invention relates to the technical field of polymer electrolyte, in particular to a self-repairing type gel polymer electrolyte membrane, a preparation method and application in an energy storage battery, the self-repairing type gel polymer electrolyte membrane is prepared by the following steps: dissolving amino-terminated polyethylene glycol in an organic solvent, adding trimesic acid under the protection of an inert atmosphere, heating, stirring and reacting to form a pre-polymerized solution, cooling, and then adding trimesic acid into the pre-polymerized solution to prepare a self-repairing type gel polymer electrolyte membrane; the preparation method comprises the following steps: adding glyoxylic acid and glacial acetic acid, carrying out a constant temperature reaction to obtain a solution A, adding LiTFSI into the solution A, carrying out ultrasonic dispersion to a homogeneous phase, pouring the obtained slurry onto a template, and carrying out a drying curing reaction to obtain the self-repairing gel polymer electrolyte membrane. A rigid aromatic cross-linking agent is used for inhibiting polymer crystallization and improving mechanical integrity, an imine bond-based dynamic covalent network is introduced to realize an autonomous interface repairing function at the working temperature of the battery, and meanwhile, a polyethylene glycol ether oxygen chain is used for constructing an efficient lithium ion transmission channel; therefore, the technical boundary that the conductivity, the mechanical strength and the interface stability of the traditional GPE are difficult to collaboratively optimize is broken through.

The invention relates to a special engineering plastic polyethersulfone microcellular foam material and a preparation method thereof, belongs to the technical field of high polymer material foaming, and solves the problem that high foaming ratio, a microcellular structure and excellent mechanical properties cannot be simultaneously obtained when a macromolecular polyethersulfone material adopts an injection foaming technology in the prior art. The method comprises the following steps: step 1, pretreating raw materials; 2, melt blending: mixing the PES base material, the second component, the functional filler, the cross-linking agent and the foam stabilizer, carrying out melt blending, granulating, and drying to obtain granules; 3, injection foaming: injecting the granules into an injection machine, adding a composite foaming agent into the injection machine, mixing, and performing injection foaming molding to obtain an injection-molded foaming material; and 4, curing: irradiating the injection-molded foam material with rays to obtain the special engineering plastic PES microcellular foam material.

The invention belongs to the technical field of adhesives, and particularly relates to a preparation method of a polysaccharide-based reversible bonding adhesive for constructing a dynamic covalent bond network. The preparation method comprises the following steps: by taking lipoic acid and sodium alginate as reactants and ferric chloride as a cross-linking agent, carrying out cross-linking reaction under a stirring condition to obtain a lipoic acid adhesive, namely the polysaccharide-based reversible bonding adhesive. According to the invention, renewable biomass resources such as sodium alginate, hyaluronic acid, chitosan and the like are used as main raw materials, so that the adhesive is expected to replace a traditional synthetic adhesive depending on a petroleum base, accords with a sustainable development strategy, contributes to reducing consumption of fossil resources, avoids release of toxic substances such as formaldehyde and the like in the synthesis and use processes, and has a good application prospect. And the method is more environment-friendly. The bio-based polysaccharide raw material has good biocompatibility and degradability, and an ideal base material is provided for developing a green and safe biomedical adhesive.

The invention relates to the technical field of food packaging materials, in particular to a cerium dioxide nano-enzyme modified antibacterial coating and application of the cerium dioxide nano-enzyme modified antibacterial coating in food packaging. The biomimetic mineralization layer comprises the following components in percentage by weight: 35-45% of a green base material, 8-12% of dopamine modified yttrium-doped cerium dioxide nano-enzyme, 4-6% of a composite antibacterial agent, 3-4% of a natural cross-linking agent, 2-3% of a degradable plasticizer, 1-2% of a biomimetic mineralization layer precursor and the balance of deionized water, the green base material is a blend of a chitosan-polyethylene glycol graft and polylactic acid; the doping amount of Y3 in the nano enzyme is 3-4at%. The antibacterial agent is excellent and lasting in antibacterial effect, has no migration risk of the antibacterial agent, and can guarantee food safety; a green base material and a degradable plasticizer are adopted, so that natural degradation is realized, and environmental pollution is avoided; the mechanical property is good, the aging resistance is realized, and the oxygen barrier property is strong; the food packaging box is suitable for various foods, effectively prolongs the shelf life, and meets the requirement of green packaging.

The invention discloses a dynamic borate bond-based self-healing polyacrylic acid binder and a preparation method thereof. The dynamic borate bond-based self-healing polyacrylic acid binder comprises a polymer main chain and a dynamic cross-linking agent, the dynamic cross-linking agent is a polyol compound containing at least two pairs of ortho-hydroxyl groups; the polymer main chain is formed by copolymerizing the following monomers: an acrylic structural monomer, the molar fraction of which accounts for 85-94% of the total monomer; a functional monomer containing a boric acid group, wherein the molar fraction of the functional monomer accounts for 3-8% of the total monomer; the mole fraction of the flexible monomer containing the acrylate group accounts for 3-8% of the total monomer. Various stresses generated by different negative electrode materials in circulation can be effectively adapted and buffered through a network formed by dynamic boric acid ester bonds and reversible fracture and combination of the boric acid ester bonds, so that the service life of the battery is generally prolonged, the working temperature range of the battery can be remarkably widened, the low-temperature discharge capacity can be remarkably increased, and the high-temperature cycle life can be prolonged.

The invention discloses a reprocessable solid-solid phase change material based on dynamic borate bonds and a preparation method of the reprocessable solid-solid phase change material. Based on the mechanism that boric acid ester is subjected to ester exchange during thermal stimulation, a dynamic cross-linking agent containing boric acid ester is adopted for cross-linking a polyurethane prepolymer, polyethylene glycol is cross-linked through chemical bonds, the tensile strength and the elongation at break of the phase change material are improved, and the problem that the phase change material is prone to leakage in the phase change process is solved; besides, borate bonds belong to associated dynamic covalent bonds and can keep the crosslinking density of the material unchanged when ester exchange occurs under thermal stimulation, so that the thermal stability of the material is relatively good; the solid-solid phase change material disclosed by the invention is excellent in mechanical property, has a relatively high enthalpy value, can be reprocessed, and has an application prospect in the fields of thermal management, energy storage, infrared stealth and the like.

The invention belongs to the technical field of new energy materials, and particularly relates to siloxane crosslinking modified polyether solid electrolyte and a preparation method thereof. According to the solid electrolyte, the electrophilic ring-opening polymerization reaction of a polymer monomer with an epoxy group is utilized, siloxane is used as a cross-linking agent, polyether chain structures are connected together to form a cross-linked network structure, the ionic conductivity can be increased, and the mechanical strength and the high-temperature dimensional stability can be improved; the lithium ion transference number is increased, the polarization is reduced, and the battery rate capability is improved; the oxidation stability of the electrolyte is improved; the decomposition reaction of polyether at high temperature is inhibited; the thermal stability and the flame retardant property of the polymer electrolyte are remarkably improved, so that the safety of a solid-state battery is improved.

The invention discloses a superconducting carbon black co-production method based on directional refining of catalytic slurry oil and a product thereof, and belongs to the technical field of carbon black preparation, and the method comprises the following steps: mixing the catalytic slurry oil and catalytic circulating oil to obtain mixed slurry oil, and adding a deliming agent for settling separation to obtain purified slurry oil; carrying out continuous solvent extraction on the obtained purified oil slurry to respectively obtain an aromatic component and a heavy component; carrying out thermal polycondensation reaction on the obtained aromatic component in a magnetic field environment in the presence of a catalyst and a cross-linking agent, and then carrying out supercritical fluid extraction to obtain spinnable mesophase pitch; carrying out slurry reactor hydrogenation deconstruction on the obtained heavy component to obtain stable micromolecular carbon black raw oil, mixing the carbon black raw oil with a nitrogen source and a template precursor, carbonizing, and carrying out acid pickling to obtain the superconducting carbon black; through a heavy oil slurry reactor hydrogenation deconstruction'doping-template 'synergistic carbonization strategy, the superconductive carbon black with nitrogen / phosphorus co-doped and developed hierarchical porous structure is constructed in situ by a one-step method.

The invention discloses a preparation method and application of self-crosslinking hydrogel containing a capsaicin functional structure, and belongs to the technical field of dye adsorption materials. The capsaicin functional structure monomer is introduced into an acrylic acid system, so that the self-crosslinking of the hydrogel is realized, and meanwhile, the adsorption performance of the hydrogel is remarkably improved; mono-substituted capsaicin functional structure monomers containing carboxyl and sulfonic acid groups are used as components, a disubstituted capsaicin functional structure monomer with polyhydroxy and carboxyl is used as a cross-linking agent, the self-crosslinking hydrogel with multiple adsorption sites is successfully constructed through free radical polymerization, and the adsorption capacity and efficiency of the hydrogel are greatly improved. The hydrogel-based carbon material is obtained by carbonizing the self-crosslinking hydrogel containing the capsaicin functional structure, the adsorption performance of the hydrogel material is further improved, the obtained hydrogel-based carbon material can be desorbed and recycled in ethyl alcohol, and the service life of the hydrogel-based carbon material is prolonged. And the problem of secondary pollution of the existing hydrogel material in the acid / alkali desorption process is effectively avoided.