7617 results about "Phenyl group" patented technology

The invention discloses a novel synthetic method for 5-phenyl tetrazole, which includes the following steps: firstly performing acid neutralization to hydrazine hydrate; then adding mixing solution formed by cyanobenzene, water and ethyl alcohol to generate phenyl aminoguanidine salt; adopting sodium nitrite for diazotization to obtain nitrine amidine under the acidic condition; obtaining 5-phenyl tetrazole crude product through closed loop under the alkaline condition; obtaining 5-phenyl tetrazole acceptable product through adopting ethyl alcohol for refining. The method has the advantages of simple technology, simplicity in operation and high product yield.

The invention relates to a crown ether covalent organic framework material as well as a preparation method and application thereof. The preparation method comprises the following steps: dissolving a crown ether monomer and an amino monomer in an o-dichlorobenzene solvent, adding a catalyst acetic acid aqueous solution, and uniformly dispersing to form a reaction solution; the method comprises the following steps: freezing a reaction solution through a liquid nitrogen bath, vacuumizing, filling nitrogen, carrying out a heating reaction, and carrying out post-treatment operations such as washing and drying on a reaction product, so as to obtain the crown ether covalent organic framework material BADT-DB18C6-COF. The crown ether covalent organic framework material is formed by condensation of a crown ether aldehyde monomer and an amino monomer, the crown ether monomer is 4, 4 ', 4' ', 4 '''-(6, 7, 9, 10, 17, 18, 20, 21-octahydrodibenzo [B, K] [1, 4, 7, 10, 13, 16] hexaoxacyclo octadecene-2, 3, 13, 14-tetrayl) tetrabenzaldehyde, and the crown ether monomer is 4, 4 ', 4' ', 4'''-(6, 7, 9, 10, 17, 18, 20, 21-octahydrodibenzo [B, K] [1, 4, 7, 10, 13, 16] hexaoxacyclo octadecene-2, 3, 13, 14-tetrayl) tetrabenzaldehyde. The amino monomer is 4 ', 5'-bis (4-aminophenyl)-[1, 1 ': 2', 1 ''-terphenyl]-4, 4''-diamine. The crown ether covalent organic framework material BADT-DB18C6-COF prepared by the invention is mainly used as an adsorbent, is used for adsorbing and recovering uranium, thorium and americium ions from a solution, shows good adsorption capacity on radionuclides U-238, Th-232 and Am-243, and is particularly suitable for the field of spent fuel post-treatment in the nuclear industry.

The invention belongs to the technical field of OLEDs, and provides a polycyclic compound containing triphenyl silicon and a polyalkyl substituent group and an organic electroluminescent device containing the polycyclic compound. The structural general formula of the polycyclic compound is as shown in formula I in the specification. Benzofuran with higher electronegativity is introduced to a ring structure composed of nitrogen atoms and boron atoms, triphenyl silicon is introduced to the para-position of boron, and the synergistic effect of benzofuran and triphenyl silicon can significantly enhance the multiple resonance of a light-emitting core and reduce vibration relaxation. Due to simultaneous use of the benzofuran and the triphenyl silicon, the problems of vibration relaxation increase, spectrum widening and the like caused by introduction of the polyalkyl substituent are remarkably improved, the luminous efficiency of the material is remarkably improved, and the color purity is improved, so that the requirement of BT.2020 wide color gamut display standard on a luminescent spectrum is met. I

The invention relates to the technical field of preparation of organic photoelectric materials, in particular to an electron transport material, an OLED with the electron transport material and an organic light-emitting device with the electron transport material. According to the electron transport material disclosed by the invention, triazinyl is taken as a framework, phenyl and cyano-substituted biphenyl is taken as a specific substituent group, methyl, adamantyl, phenyl and pyridyl are limited to be matched, and the electron transport material is used as a material for forming an electron transport layer to manufacture an organic electroluminescent device, so that the evaporation process of the device can be smoothly carried out; and the light-emitting efficiency of the organic light-emitting device is effectively improved, and the application prospect is very good.

The invention relates to the technical field of dielectric materials, and discloses polyimide, a polyimide film and a preparation method and application thereof, the polyimide is obtained by a polymerization reaction of a dianhydride monomer and a diamine monomer, the diamine monomer comprises a methylene bridging group and a phenyl group with a substituent group, and the methylene bridging group is a phenyl group with a substituent group. The substituent group at least comprises one methyl group. The molecular twisted conformation lock structure provided by the invention not only can improve the tolerance of polyimide, but also can doubly inhibit intrachain and inter-chain charge migration of the dielectric film, so that the dielectric film still has extremely high energy storage density and energy storage efficiency at a service temperature close to a glass-transition temperature.

The invention relates to the technical field of high polymer material chemistry, and discloses a high and low temperature resistant anti-yellowing optical adhesive and a preparation process thereof, the high and low temperature resistant anti-yellowing optical adhesive comprises the following components by weight: 40-60% of modified organic silicon resin, 20-30% of urethane acrylate, 10-15% of alicyclic epoxy resin, 0.5-5% of a nano inorganic filler, 0.8-2.5% of an anti-yellowing composite reagent, and the balance of a solvent. The coating is prepared from the following components in percentage by weight: 0.5 to 1.5 percent of 2-hydroxy-2-methyl-1-phenyl-1-acetone, 0.1 to 0.3 percent of fluorine modified polyacrylate flatting agent and 0.3 to 1.0 percent of chloroplatinic acid-divinyl tetramethyl disiloxane complex catalyst. The preparation method comprises the following steps: mixing alpha, omega-dihydroxy polydimethylsiloxane and phenyltrimethoxysilane according to a mass ratio of 8: 2-7: 3, adding 0.3-1.0% of a chloroplatinic acid-divinyl tetramethyl disiloxane complex catalyst, and raising the temperature by stages under the protection of nitrogen, so that the glass transition temperature of the adhesive can reach 120 DEG C below zero and 125 DEG C, and the temperature of the adhesive can reach 120 DEG C below zero and 125 DEG C below zero. And the long-term service requirement of the optical device in an extreme temperature environment is met.

The invention discloses a preparation method of high-purity diiodosilane, which comprises the following steps: firstly, preparing a p-phenylsilane solution from phenyl trichlorosilane and sodium hydride as raw materials, rectifying and purifying the p-phenylsilane solution, directly reacting the p-phenylsilane solution with iodine to generate diiodosilane, and reacting phenylsilane with iodine to directly generate diiodosilane; in the process of preparing diiodosilane from phenylsilane, conditions are mild, the reaction process is controllable, the reaction time is shortened by controlling the temperature in the synthesis process and increasing the pressure of a reaction system, hydrogen iodide overflow is reduced, sodium hydride is adopted as a reducing agent in the reaction process, and the yield of diiodosilane is increased. The solid waste can be recycled, the cost can be effectively reduced, and industrialization of diiodosilane is facilitated.

The invention belongs to the technical field of biological dyes, and discloses a bio-based melanin precursor compound, bio-based melanin as well as a preparation method and application of the bio-based melanin precursor compound and the bio-based melanin. The invention provides a bio-based melanin precursor compound 4-[5-(2, 2-diaminoethyl)-2, 3-dihydroxyphenyl]-1H-indole-5, 6-diphenol, and a preparation method of the bio-based melanin precursor compound. The bio-based melanin precursor compound is stable in chemical property and easy to store. And the catalyst can be used as a raw material to efficiently synthesize bio-based melanin through a catalytic oxidation reaction. The process for preparing the bio-based melanin is simple, mild, high in yield and suitable for large-scale industrial production. The bio-based melanin prepared by the invention has good application performance during dyeing, does not generate harmful substances, and is safe and environment-friendly.

The invention provides a method for synthesizing 1, 2-bis (4-vinyl phenyl) ethane, which comprises the following steps: adding a first solvent, methyl triphenyl phosphine halide and strong alkali into a reaction flask, and uniformly stirring to obtain a first mixed solution; heating the first mixed solution and carrying out reflux reaction for 1 hour; dropwise adding a 1, 2-bis (p-formaldehyde phenyl) ethane solution until the reflux reaction is finished to obtain a second mixed solution; reducing the temperature of the second mixed solution to room temperature, and adjusting the pH value of the second mixed solution to obtain a first solution; layering the first solution, and taking an organic layer; adding a polymerization inhibitor into the organic layer to obtain a second solution; concentrating the second solution to obtain a 1, 2-bis (4-vinyl phenyl) ethane crude product; adding a poor solvent into the crude product, stirring and crystallizing; filtering the crystal to obtain a filter cake, adding a second solvent into the filter cake, and washing and drying the filter cake to obtain 1, 2-bis (4-vinyl phenyl) ethane; the method for synthesizing the BVPE is simple and low in raw material cost, and the synthesized BVPE is high in purity and free of product isomeride.

The invention is applicable to the technical field of intelligent response materials, and provides a three-dimensional azobenzene functionalized covalent organic framework intelligent response material and a preparation method thereof. The three-dimensional azobenzene functionalized covalent organic framework intelligent response material is prepared by uniformly grinding 3, 3 ', 5'-tetra [(3 ', 5'-diformylphenyl)]-hexamethyl biphenyl and azobenzene-4, 4 '-diaminotriphenylamine, adding an organic solvent, adding a catalyst acetic acid aqueous solution, quickly freezing, emptying air, sealing with flame, heating after recovering to room temperature, and obtaining the three-dimensional azobenzene functionalized covalent organic framework intelligent response material. According to the invention, the azobenzene functionalized covalent organic framework material with a bcu topological structure is synthesized; the material has excellent photostimulation response CO2 adsorption performance; reversible control of CO2 adsorption capacity can be realized through ultraviolet light and heating conditions, at least five times of circulation can be maintained, and good circulation stability is achieved.

The invention relates to a high-stability bronze powder pigment and a preparation method and application thereof.The preparation method comprises the following steps that copper-zinc alloy coarse powder, stearic acid and a dissolved compound passivator are taken and subjected to ball milling in the nitrogen atmosphere, and a ball milling product is screened, washed and subjected to suction filtration to obtain an amino-functionalized passivated base material; the preparation method comprises the following steps: dispersing SiO2 in anhydrous isopropanol to obtain a reaction system, adding deionized water and a catalyst, dissolving tetraethoxysilane and phenyltriethoxysilane in anhydrous isopropanol, slowly dropwise adding, carrying out a heat preservation reaction, and carrying out suction filtration and washing to obtain a phenyl modified SiO2 coated intermediate; the preparation method comprises the following steps: dispersing a compound stabilizer in anhydrous isopropanol to obtain a mixed system, heating and stirring, dissolving the compound stabilizer in anhydrous isopropanol, dropwise adding into the mixed system, reacting, centrifuging, washing, and drying in vacuum to obtain the bronze powder pigment. The bronze powder pigment disclosed by the invention has excellent oxidation resistance, chemical corrosion resistance and long-term storage stability, and can keep the natural color gloss of metal to the greatest extent.

The invention relates to the field of cables, and discloses a modified polyvinyl chloride composite material for cables and a preparation method thereof.The composite material comprises low-density polyethylene, polyvinyl chloride, ethylene-vinyl acetate copolymer, nitrile rubber, modified graphene oxide, modified nano calcium carbonate and auxiliaries; the modified graphene oxide is prepared by reacting acylating chlorination of graphene oxide with an anti-aging derivative, the anti-aging derivative is prepared by reducing a benzoxazole-containing intermediate generated by a reaction of 2-amino-4-bromophenol and 4-cyanobenzaldehyde to obtain an aminated benzoxazole-containing intermediate, then the aminated benzoxazole-containing intermediate reacts with p-phenylenediamine, and then the product reacts with 3-(3, 4-dichlorophenyl)-1, 2, 3-triazole-3-one to obtain the anti-aging graphene oxide. 2, 5-di-tert-butyl-4-hydroxyphenyl) propionyl chloride is subjected to a reaction to prepare the product. And the modified nano calcium carbonate is prepared by reacting phosphonitrilic chloride trimer with an amino silane coupling agent and 2-amino benzoxazole-5-borate and then grafting on the surface of the nano calcium carbonate. The composite material prepared by the invention has excellent flame retardance, heat resistance and long-acting oxidation resistance.

The invention discloses a corrosion-resistant polysilsesquioxane modified polyurethane emulsion and a preparation method thereof, and belongs to the technical field of emulsions.The preparation method comprises the steps that gamma-aminopropyltriethoxysilane, namely APTES, is subjected to hydrolytic condensation under the catalysis of tetraethylammonium hydroxide, and POSS is prepared; the preparation method comprises the following steps: carrying out hydrolytic condensation reaction on APTES, synchronously adding phenyltrimethoxysilane in the hydrolytic condensation reaction, forming phenyl-amino difunctional POSS (Polyhedral Oligomeric Silsesquioxane) according to a molar ratio of phenyltrimethoxysilane to APTES of 1: 4, and grafting POSS and graphene oxide GO in dimethyl sulfoxide through amidation reaction to prepare a POSS / GO composite material; dispersing POSS / GO / Zn in the polyurethane prepolymer, adding a curing agent and a solvent, and stirring to form a homogeneous emulsion; through phenyl trapezoid polysilsesquioxane modification and dynamic reversible self-repairing network design, the wear resistance of the coating is improved, microcracks can be closed at the temperature of 60 DEG C, and the maintenance requirement is reduced; laser micro-nano structured base material treatment is combined, the adhesive force is increased to be larger than or equal to 20 MPa, and meanwhile a gamma-butyrolactone low-VOC solvent is adopted.

The invention discloses a comb-type polyphosphate polymeric dispersant and a preparation method thereof, the dispersant is prepared by preparing a phosphate monomer from acrylate and phosphorus pentoxide, then copolymerizing the phosphate monomer with phenyl alkene or alkyl alkene, and finally adding alkali liquor for neutralization. A phosphate-polyether bifunctional side chain is introduced to a main chain, a phosphate group provides electrostatic repulsion, and a polyether group enhances steric hindrance, so that the dispersing agent can meet the requirements of strong adsorption and long-range stability at the same time, and a more durable and effective stabilizing effect is provided for a dispersion system.

The invention relates to the technical field of PC transparent flame-retardant toughening modification, in particular to phenolic hydroxyl-terminated modified polysiloxane with a side chain containing phenyl and sulfonate groups and a preparation method of copolymerized PC. The modified polysiloxane is prepared by the following steps: performing ring opening polymerization on phenol-containing double end sockets and cyclotetrasiloxane to obtain modified polysiloxane containing double bonds and phenyl functional groups, and grafting sulfonate through a thiol-ene click chemical reaction. Diphenyl carbonate, bisphenol A and the modified polysiloxane are used as raw materials, a polysiloxane-PC block copolymer is formed through copolymerization, efficient flame retardance and high transparency are achieved, and meanwhile extremely high low-temperature impact strength is achieved.

Stable and bioavailable formulations and dosage forms comprising a dispersion (e.g., spray-dried dispersion) of solid amorphous 6-(cyclopropancamido)-4-((2-methoxy-3-(1-methyl-1H-1,2,4-triazol-3-yl)phenyl)amino)-N-(methyl-d3)pyridazine-3-carboxamide (Formula (I): BMS-986165) in a solid polymer matrix are provided for the treatment of auto-immune and auto-inflammatory diseases such as an inflammatory bowel disease (IBD) and psoriasis.

The invention discloses a hydrogel wound dressing with a synergistic healing promoting function as well as a preparation method and application thereof. The preparation method comprises the following steps: 1, dissolving oxidized methacrylated hyaluronic acid and dopamine in deionized water to obtain a solution A; the preparation method comprises the following steps: dissolving N-isopropylacrylamide, a photoinitiator 2-hydroxy-2-methyl-1-(4-(2-hydroxyethoxy) phenyl)-1-acetone and a cross-linking agent N, N '-methylene bisacrylamide in deionized water to obtain a solution B; 2, mixing the solution A and the solution B to obtain a pre-gel solution; or dissolving polyphenylboronic acid ester nanoparticles or polyphenylboronic acid ester-kaempferol with deionized water to obtain a solution C, and mixing the solution C with the solution A and the solution B to obtain a pre-gel solution; and 3, injecting the pre-gel liquid into a mold, and illuminating to obtain the hydrogel wound dressing loaded with the nanoparticles. The hydrogel disclosed by the invention can be used for effectively solving various problems in a wound healing process and promoting rapid and high-quality healing of a wound.

The invention provides a preparation method of a hyperbranched polyimide-derived silicon-carbon negative electrode material, which comprises the following steps: S1, preparation of a carbon precursor: mixing 1, 3, 5-tris (4-aminophenyl) benzene and 4, 4 '-(hexafluoroisopropenyl) diphthalic anhydride for reaction to prepare hyperbranched polyimide; s2, preparing porous carbon; and S3, vapor phase silicon carbon deposition. The invention also correspondingly provides a silicon-carbon negative electrode, a lithium ion battery and an electrochemical device. According to the hyperbranched polyimide-derived silicon-carbon negative electrode material, the volume expansion of silicon in the lithium intercalation process is effectively relieved, the active material is prevented from falling off, and the cycling stability of the battery is improved.

The present disclosure provides crystalline and amorphous forms of 6-fluoro-7-(2-fluoro-6-hydroxyphenyl)-1-(4-methyl-2-(2-propanyl)-3-pyridinyl)-4-((2S)-2-methyl-4-(2-propenoyl)-1-piperazinyl)pyrido[2,3-d]pyrimidin-2(1H)-one, including several anhydrous, hydrate and solvate forms, and solid state forms thereof, pharmaceutical compositions, and methods of treating a disease mediated by KRAS G12C inhibition.

The invention discloses a heat dissipation type anti-corrosion coating and a preparation method thereof, and belongs to the technical field of anti-corrosion coatings. The heat dissipation type anticorrosive paint comprises a component A and a component B, wherein the component A comprises the following components in parts by mass: 100 parts of heat-conducting water-borne epoxy resin, 4-6 parts of graphene, 0.3-0.5 part of an antioxidant, 0.2-0.4 part of a defoaming agent, 0.2-0.4 part of a flatting agent and 10 parts of first deionized water; the component B comprises the following components in parts by mass: 10-20 parts of a curing agent, 40-60 parts of a toughening agent, 4-6 parts of functionalized boron nitride microspheres and 30-50 parts of second deionized water; the heat-conducting water-borne epoxy resin is 1, 5-naphthalene diphenol modified water-borne epoxy resin; the curing agent is an aromatic amine curing agent; the toughening agent is obtained by carrying out copolymerization on acrylamide, N-(4-aminophenyl) acrylamide, 1, 3, 5-triacryloyl-s-triazine and 3-dimethylamino allyl phosphoric acid; the functionalized boron nitride microspheres are boron nitride microspheres modified by 4-aminobenzoic acid.

The invention discloses a carrier-free nano-particle with pH / ROS dual response as well as a preparation method and application of the carrier-free nano-particle. The preparation method comprises the following steps: enabling quinolizidine alkaloid and flavonol to be subjected to self-assembly, so as to prepare quinolizidine alkaloid-flavonol carrier-free nano particles; modifying the quinolizidine alkaloid-flavonol carrier-free nano particles by adopting a phenylboronic acid-hyaluronic acid conjugate, so as to prepare nano particles modified by the phenylboronic acid-hyaluronic acid conjugate; and coating the surfaces of the nano-particles modified by the phenylboronic acid-hyaluronic acid conjugate with a pH sensitive polymer to prepare the pH / ROS dual-response carrier-free nano-particles. The sophocarpidine-kaempferol carrier-free nanoparticles with pH / ROS dual response, prepared by the invention, have the advantages of good targeting property, high biocompatibility, small toxicity and adverse reaction and the like, meanwhile, the nanoparticles have a good anti-inflammatory effect, and a new choice is provided for the treatment of ulcerative colitis.

The invention discloses a low-temperature-resistant organic silicon elastic damping body and a preparation method thereof, and belongs to the field of synthesis of organic polymer materials. The invention relates to a high-efficiency photoinitiator, which is prepared from the following ingredients in parts by weight: 95 to 110 parts of fluorosiloxane-phenylsiloxane segmented copolymers, 25 to 35 parts of boric acid ester end-capped polyurethane prepolymers, 10 to 15 parts of neodymium-containing metal organic frameworks, 20 to 40 parts of azobenzene modified CNT / TiO2, 2 to 4 parts of photoinitiators 1173 and 2 to 3 parts of neodymium acetylacetonate. Ultralow-temperature adaptability, self-repairing and high-modulus coexistence and wide-temperature-range damping stability are achieved through fluorosilicone / phenyl block copolymer molecular design, a borate-neodymium coordination double-dynamic network, stress response filler and a light-heat gradient curing process. The low-temperature-resistant organic silicon elastic damping body prepared by the invention provides a new solution idea for an extreme environment damping material, and has a wide application prospect.

The invention relates to the technical field of water treatment, in particular to a reverse osmosis membrane and a preparation method thereof. The preparation method of the reverse osmosis membrane comprises the following steps: soaking a base membrane in a water phase solution, taking out the base membrane, drying the surface of the base membrane, coating the base membrane with an oil phase solution, carrying out interfacial polymerization reaction, curing, coating with a modifier solution, and drying to obtain the reverse osmosis membrane, the modifying agent comprises 2, 4, 6-tri (4-aminophenyl)-1, 3, 5-triazine-1, 3, 5-tri (4-methyl phenyl) benzene. The successfully grafted COFs can improve the water permeability of the membrane to a certain extent, and also can improve the pollution resistance, acid resistance and oxidation resistance of the membrane, so that the service life of the membrane is prolonged. According to the invention, different effects of the same type of imino COFs introduced to the reverse osmosis membrane are further compared, so that the excellence of the selected imino COFs is highlighted.

The invention relates to the technical field of electric power facilities, in particular to a high-strength flame-retardant fireproof cable and a preparation method thereof. The phosphonitrile flame retardant is prepared by adding phosphonitrilic chloride trimer, phenylphosphonic acid, triethylamine and melamine. Then, 9, 10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide, the modified carbon nanotubes and the flame-retardant modified halloysite nanotubes are used as main raw materials, and the flame-retardant filler is prepared. The preparation method comprises the following steps: mixing polyolefin, a phosphazene flame retardant, a flame-retardant filler, talcum powder, gum and stearic acid, fully stirring and melting to obtain a sizing material, and carrying out crosslinking, granulation and molding on the sizing material to obtain the cable protection sleeve. And wrapping the outermost layer of the cable with the cable protection sleeve to obtain a finished cable. The finished cable prepared by the invention has good flame retardance and mechanical strength, so that the cable has a wide application prospect in the technical field of electric power facilities.

The present invention relates to the field of water treatment technology, and more particularly to a kind of reverse osmosis membrane and preparation method thereof.The preparation method of the reverse osmosis membrane includes:Basement membrane is soaked in aqueous phase solution, after taking out surface drying, oil phase solution is coated on basement membrane and carries out interfacial polymerization reaction, after solidification, coating modifier solution, after drying, obtain reverse osmosis membrane;The modifier includes 2,4,6-tris (4-aminophenyl) ‑1,3,5-triazine ‑1,3,5-tris (4-methylphenyl) benzene.The COFs successfully grafted by the present invention can improve the water permeability of membrane to a certain extent, and can also improve the anti-pollution property, acid resistance and oxidation resistance of membrane, and then improve the service life of membrane.The present invention further compares the different effects that the same type of imino COFs are introduced into reverse osmosis membrane, so as to highlight the excellence of the imino COFs selected by the present invention.

The invention relates to the technical field of luminescent materials, and discloses an aggregation-induced emission material, nanoparticles as well as a preparation method and application thereof, the structural general formula of the aggregation-induced emission material is as follows: # imgabs0 #, R is selected from one of the following structures: # imgabs1 # aggregation-induced emission material takes a pyridine group as an acceptor unit, and the acceptor unit is selected from one of the following structures: 1 # imgabs2 # aggregation-induced emission material; a carbon-carbon double bond and a thiophene unit are used as pi bridges, and diphenylamine, bis (4-ethylphenyl) amine and bis (4-(tert-butyl) phenyl) amine are used as strong electron donors. The donors not only provide strong electron supply ability, but also become efficient rotors due to highly twisted molecular conformation, and endow the aggregation-induced emission material with long emission wavelength and aggregation-induced emission activity.

The invention relates to an in-situ curing gel structure electrolyte as well as a preparation method and application thereof. The preparation method comprises the following steps: (1) mixing a resin matrix with a pore-forming agent, then adding a curing agent for mixing to obtain a mixed solution, and pouring the mixed solution into a closed mold for curing to obtain a resin film; soaking and drying the resin film to obtain porous resin; and (2) mixing 4-styrene sulfonyl (phenylsulfonyl) imide lithium salt, polyethylene glycol methyl ether acrylate, polyethylene glycol dimethacrylate, ethylene carbonate and azodiisobutyronitrile to prepare a mixed solution, and soaking the porous resin in the mixed solution to react and cure, thereby obtaining the in-situ curing gel structure electrolyte. The preparation method is simple, and the prepared in-situ curing gel structure electrolyte can improve the mechanical property, the battery capacity and the cycle performance of the in-situ curing gel structure electrolyte.

The invention discloses a composite film based on light-biological synergistic gradient degradation and a preparation method thereof, the composite film sequentially comprises a light response layer, a transition layer and a biological response layer from outside to inside, and the light response layer comprises a polycaprolactone matrix, a tetraphenylporphyrin iron photosensitizer and anatase type TiO2 nanorods; the transition layer is a gradient blend of polylactic acid and modified starch; the biological response layer comprises polyhydroxyalkanoate and bacterial cellulose nanofibers; through the design of the three-layer gradient structure and the construction of the bionic microchannel, the synergistic effect of light degradation, hydrolysis and biodegradation is realized; the composite membrane has excellent mechanical properties and environmental adaptability, the degradation period can be accurately regulated and controlled within 30-180 days, and the soil degradation rate within 60 days reaches 91% or above; the preparation method comprises the processes of electrostatic spinning, gradient co-extrusion and bacterial cellulose in-situ culture. The material can be widely applied to the fields of agricultural mulching films, food packaging and the like, and the problems that a traditional degradable film is poor in mechanical property and uncontrollable in degradation are solved.

The invention relates to the technical field of preparation of organic photoelectric materials, in particular to an organic light-emitting device and a display or lighting device comprising the organic light-emitting device. A hole transport layer compound of the device is obtained by taking a phenyl and alkyl fixed substituted fluorenyl structure as a core fragment and taking a benzo five-membered ring and a limited substituted benzene ring as two side chains of amido, and is matched with a limiting material of a light-emitting auxiliary layer to manufacture an OLED (Organic Light Emitting Diode) element; the light-emitting efficiency and the working life of the organic light-emitting device are effectively improved, and the application prospect is very good.

The invention relates to an optical monomer and a preparation method and application thereof, the structural general formula of the optical monomer is as follows: R1, R2 and R3 are respectively selected from one of hydrogen and C1-C4 alkyl, A1 is selected from one of hydrogen and C1-C4 alkyl, and A2 is C1-C4 alkyl; r4 is selected from one of H, phenyl and C1-C4 alkyl, and A2 is C1-C4 alkyl; and R5 is hydrogen or methyl. The optical monomer provided by the invention contains a (methyl) acrylate group, and has the properties of high refractive index and low volume shrinkage; and a plurality of aromatic rings with high molar refractive index and low molar volume are contained, so that the whole molecule of the whole monomer is extremely high in refractive index. The monomer structure provided by the invention has a plurality of branched chains, the overall molecular weight is small, and the molecules are not easy to agglomerate.