1688 results about "Benzene" patented technology

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 invention discloses a crown ether grafted polyarylether sulfone ion separation membrane as well as a preparation method and application thereof, and belongs to the technical field of ion separation membranes, collaborative optimization is realized through crown ether accurate grafting and ultrathin ordered membrane formation: a main chain of polyarylether sulfone is grafted with 4 '-aminobenzo-12-crown-4 to form an inherent channel adapted to Li, and the specific surface area of the main chain is increased; the ultrathin film is prepared by a water surface spreading method, and the ion transmission path is shortened. Finally, in a LiCl / MgCl system, Liion flux has high selectivity, high permeation-high selectivity cooperation is preliminarily realized, the chemical synthesis step can be amplified to a kilogram level, and after a DPAES-g-CE / dichloromethane solution is dropwise added to the water surface, the DPAES-g-CE / dichloromethane solution is rapidly spread to form a film without precise equipment; the raw materials are industrial-grade monomers and have no toxic residues, the membrane can be recycled and reused through dichloromethane, the equipment cost is reduced by about 90%, and industrialization is easy; the main chain of the polyaryl ether sulfone is high in rigidity and resistant to high temperature and chemical corrosion; crown ether grafting avoids molecular chain agglomeration, and the swelling rate is far lower than that of a traditional sulfonated membrane.

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 a cellulose-chitosan-based lithium ion battery diaphragm and a preparation method and application thereof.The preparation method of the diaphragm comprises the steps that gamma-polyglutamic acid and polyamide epichlorohydrin are adopted for modifying chitosan, the hydrophilicity and the liquid absorption capacity of the chitosan are improved, polyvinylpyrrolidone is adopted for coating the chitosan, and the hydrophilicity and the liquid absorption capacity of the chitosan are improved; pVP is replaced in ethanol soaking to form micropores, so that the porosity of the modified chitosan is improved. Amino groups and hydroxyl groups of the modified chitosan are combined with catechol of the polydopamine and hydroxyl groups of the hydroxy propyl cellulose through hydrogen bonds and covalent bonds to form a chitosan-cellulose-PDA interpenetrating network, and the diaphragm material suitable for the lithium ion battery is finally prepared by combining hot-pressing shaping. The preparation method has the advantages that the balance between the mechanical property and the ion conduction property of the diaphragm is realized through multi-component compounding by utilizing the biocompatibility and renewability of natural macromolecules (cellulose and chitosan).

The invention discloses a memristor based on a covalent organic framework and a preparation method and application thereof.The memristor comprises a substrate, a semiconductor electrode, a covalent organic framework film and a metal electrode which are sequentially arranged in a stacked mode, and the covalent organic framework film is composed of 1, 3, 4, 5, 6, 7, 8, 8, 9, 10, 11, 12, 13, 14, 16, 17, 17, 17, 17, 17, 17, 17, 17, the catalyst is prepared by condensing 1, 3, 5-tri (4-aminophenyl) benzene and terephthalaldehyde or terephthalaldehyde with an alkyl or alkoxy side chain. The covalent organic framework film has a highly ordered structure and an adjustable porous structure, the preparation process is simple, the film thickness is uniform, the flatness and the crystallinity are high, and the dielectric property is adjusted, so that the switching voltage and the cycling stability of the memristor are adjusted, and the memristor has stable and repeatable switching performance; the COFs-based memristor has high on / off ratio, low device variability and high flexibility, can be used for preparing the COFs-based memristor, can provide technical support for neuromorphic devices with high efficiency, adjustability, structure adjustability and rich functions, and can be applied to the field of intelligent sensing and autonomous system control such as an auxiliary driving system.

The invention relates to the technical field of biological medicines, and particularly discloses a BODIPY (boron dipyrromethene)-based compound and an application of the BODIPY-based compound in photodynamic oxidation of beta-amyloid protein (Abeta). The compound takes iodo-BODIPY as a photosensitive core and is connected with 4-t-butyloxycarboryl benzene as an A beta recognition group. The introduction of iodine atoms significantly enhances the intersystem crossing ability of molecules, so that the molecules have excellent reactive oxygen species (ROS) generation ability. The compound has high ROS yield, good optical stability and biocompatibility, can specifically target A beta aggregate, realizes photodynamic oxidative degradation, and provides a novel potential tool for treatment of Alzheimer's disease.

The invention relates to a preparation method of a ZIF-67 derived cobalt-manganese catalyst and application of the ZIF-67 derived cobalt-manganese catalyst in catalytic oxidation of benzene, and belongs to the technical field of catalyst preparation. The preparation method comprises the following steps: preparing a ZIF-67 precursor; dispersing ZIF-67 in water to form a turbid liquid, and adding a potassium permanganate aqueous solution to carry out an etching reaction to obtain a mixed system; transferring the mixed system into a reaction kettle for hydrothermal reaction to obtain a black precipitate; and washing the black precipitate, drying, roasting, and grinding to obtain the ZIF-67 derived cobalt-manganese catalyst. According to the preparation method, the problem that residues are usually easy to remain in the conventional preparation method of the ZIF-67 catalyst is solved, and the Co-Mn8-T140 catalyst prepared by the preparation method disclosed by the invention can realize 90% of benzene conversion rate at the reaction temperature of about 210 DEG C under the reaction conditions that the air speed is up to 60000mL / (g.h), the benzene concentration is 1000ppm and the oxygen content is 20%.

The invention discloses a sensing material for detecting atmospheric carboxylic acid, a preparation method, a detection method and application, belongs to the technical field of environmental functional materials, and solves the problems that an existing method is complex in operation and cannot realize real-time online monitoring, the sensing material for detecting atmospheric carboxylic acid is an MOF-802-EDTA-Pt composite film, and the preparation method comprises the following steps: taking 1, 3, 4, 5-tetramethyl-1, 3, 5-tetramethyl-1, 3, 5-tetramethyl-1, 3, 5-tetramethyl-1, 3, 5-tetramethyl-1, 3, 5- The preparation method comprises the following steps: synthesizing an MOF-802 material through a hydrothermal reaction by taking 1, 3, 5-benzene tricarbonic acid (BTC) and aluminum nitrate as raw materials and ethylene diamine tetraacetic acid (Na-EDTA) as a ligand; the preparation method comprises the following steps: dispersing MOF-802 in DMF to form a coating solution, and forming a film on a glass substrate through a pulling method; and then loading platinum nanoparticles, and carrying out solvothermal reaction and vacuum drying to obtain the composite sensing film. The MOF-802-EDTA-Pt composite film has a porous structure and fluorescence characteristics, and detection is realized through a fluorescence quenching effect of carboxylic acid molecules and an MOF skeleton. The method disclosed by the invention is controllable in process and high in material stability, still keeps excellent selectivity under the coexistence condition of interferents such as CO2 and NO2, and is suitable for real-time monitoring of carboxylic acid pollutants in the atmospheric environment.

The invention relates to preparation of a crystalline allyl covalent organic framework material and application research of the crystalline allyl covalent organic framework material in benzamide cyclization green photocatalytic conversion. The SF-COF material is prepared by adopting a step-by-step synthesis method. The preparation method comprises the following steps: synthesizing a COF precursor by taking 1, 3-benzenetricarboxaldehyde and p-aminophenylacetonitrile as raw materials, and preparing the allylation covalent organic framework material with the electronic push-pull effect from the COF precursor and 5, 5 ', 5'-(benzene-1, 3, 5-triyl) tri (thiophene-2-formaldehyde) through a solvothermal method. The material is applied to the field of photocatalytic organic conversion, and benzamide cyclization and conversion of derivatives of benzamide are achieved under irradiation of a blue light LED. The prepared SF-COF has the advantages of efficient charge separation and electron conduction performance, good structural stability and chemical stability and the like. And a catalyzed organic reaction substrate has the advantages of wide universality range, good cycle stability and the like, and shows excellent photocatalytic conversion capability.

The invention belongs to the technical field of luminescence and display, and particularly relates to a D-A type green light TADF material and application thereof in OLEDs. The luminescent material comprises an oxygen bridge triphenylboron acceptor unit and oxygen bridge triphenylamine which are used as donor units, and a green light TADF material is constructed through simple coupling. The rigid large plane structure of the material limits rotation of a benzene ring, vibration relaxation of a condensed ring structure is reduced, and the photoluminescence efficiency as high as 90% is obtained. Research results show that the maximum emission peak of the device is 518 nm and the maximum external quantum efficiency (EQE) of the device is 37.8% under different doping concentrations when the OLEDs are processed by the solution, especially under the doping concentration of 5-100%, the electrogenerated emission peak change of the device is small, the EQE of 30% or above is kept, the excellent concentration quenching inhibition performance is shown, and the application prospect is attractive.

The invention provides a preparation method of 2, 5-disubstituted benzyl chloride, and belongs to the technical field of preparation of drug intermediates. The chloromethyl solution is prepared from concentrated hydrochloric acid and paraformaldehyde, the concentration of hydrochloric acid is gradually reduced along with the reaction, and the reaction progress is slow due to the reduction of the concentration of concentrated hydrochloric acid; therefore, the chloromethylation reaction is carried out on the chloromethyl liquid and the disubstituted benzene in the hydrogen chloride gas, and the hydrogen chloride gas is supplemented, so that the concentration of the hydrogen chloride is increased, and the chloromethylation reaction is accelerated; meanwhile, a gradient heating mode is adopted, disubstituted benzene and chloromethyl liquid are subjected to chloromethylation reaction for 2-3 hours at the temperature of 50-60 DEG C, and the temperature is increased to 70-80 DEG C after the concentration of hydrogen chloride is reduced, so that the chloromethylation reaction is accelerated again, and the yield of the product is increased. According to the method, the volatilization and consumption of concentrated hydrochloric acid can be reduced, the generation of wastewater is reduced, the reaction time is shortened, and meanwhile, the yield of 2, 5-disubstituted benzyl chloride is also improved.

The invention discloses an EGFR (epidermal growth factor receptor) targeted nano-drug carrier and a preparation method thereof, the EGFR targeted nano-drug carrier comprises drug-loading nanoparticles, an erythrocyte membrane coating the drug-loading nanoparticles and GE11 peptide connected to the erythrocyte membrane, and the drug-loading nanoparticles are formed by connecting tannic acid, ellagic acid and 1, 4-phenyldiboronic acid through boric acid ester bonds. The EGFR targeted nano-drug carrier disclosed by the invention can be enriched at an EGFR overexpressed tumor site in a targeted manner, and can be effectively prevented from being cleared by an immune system, and the drug loaded by the drug-loaded nanoparticles is released in a high-active oxygen environment, so that the treatment effect on tumors can be improved, and the toxic and side effects on normal tissues can be reduced; and photothermal therapy and chemotherapy effects can be simultaneously generated under NIR illumination, and the anticancer efficiency can be remarkably improved through the synergistic effect of the photothermal therapy and the chemotherapy.

The invention provides an application of N '1, N' 3, N '5-tri ((E)-4-(diphenylamino) benzylidene) benzene-1, 3, 5-tricarbohydrazide (TBTCH) as a piezo-chromic material. The invention provides a novel application of the compound TBTCH, and research shows that the compound has a polycrystalline state property and a piezochromic property, and has two single crystal structures TBTCH-c and TBTCH-g which emit cyan and green fluorescence under different wavelengths; under the action of pressure, the TBTCH-g is converted into an amorphous state from an original crystalline state and is converted into a yellow state sample, and the TBTCH-g can recover to the original state after being fumigated, so that the TBTCH-g has reversible piezochromism performance; and the TBTCH-c changes color under the action of pressure and cannot recover to the original state through a conventional fumigation method, but the TBTCH-g and the TBTCH-c can realize conversion between the TBTCH-g and the TBTCH-c through recrystallization. Therefore, the compound TBTCH can be used as a photochromic material to be applied to the fields of information encryption, intelligent display, biosensing, environmental monitoring and the like.

The utility model relates to a negative-pressure crude benzene distillation system adopting a tubular furnace for heating. The negative-pressure crude benzene distillation system comprises a debenzolization tower, the tubular furnace and a crude benzene condensing, cooling and separating integrated device, the debenzolization tower is sequentially provided with a rectifying section, a stripping section, a storage tank section and a regeneration section from top to bottom; the crude benzene condensing, cooling and separating integrated device comprises a heat exchange tower and a separating tank; a low-temperature water heat exchanger is arranged at the lower part of the heat exchange tower; a crude benzene collecting section, an oil-gas-water separating section and a water collecting section are arranged in the separating tank; a first heating section and a second heating section are arranged in the tubular furnace. Compared with an existing negative-pressure crude benzene distillation process system, the negative-pressure crude benzene distillation process system has the remarkable advantages that the tail gas output is low, the tail gas is not discharged, the tube furnace operation temperature is low, the washing oil consumption is small, no additional separated water is generated, the one-time investment is low, and the like.

The invention provides a preparation method of a perovskite solar cell of a self-assembly monomolecular layer based on micromolecule modification, and relates to the technical field of preparation of solar cells, the method comprises the following steps: spin-coating a blended solution on the surface of a substrate, then performing annealing treatment, and forming a modification layer on the substrate; wherein the 1, 4-benzene diphosphonic acid is anchored on the surface of the substrate through a phosphate radical group at one end of the 1, 4-benzene diphosphonic acid, gaps among SAM molecules are filled, a uniformly covered film is formed, and meanwhile, a phosphate radical group at the other end of the 1, 4-benzene diphosphonic acid is exposed on the surface of the modification layer; depositing a perovskite precursor solution on the surface of the formed modification layer, and performing crystallization treatment to form a perovskite light absorption layer; wherein the wettability of the perovskite precursor solution on the surface of the modification layer is improved by the phosphate radical group exposed on the surface of the modification layer. According to the invention, SAM molecular gaps are filled with 1, 4-benzene diphosphonic acid (the coverage rate is greater than 99.5%), and the pinhole defect is thoroughly eliminated.

The invention relates to the technical field of liquid crystal polymers, and discloses a high-temperature-resistant, electricity-conducting and heat-conducting graphene-LCP material and a preparation method thereof.The preparation method comprises the steps that a diacid monomer, p-hydroxybenzoic acid and 4, 4 '-bis (4-hydroxyphthalimide)-benzamido benzene are subjected to a carboxyl reaction, liquid crystal polyarylester is obtained and mixed with graphene oxide, and the high-temperature-resistant, electricity-conducting and heat-conducting graphene-LCP material is obtained. The liquid crystal polyarylester molecular chain contains an imide ring, so that the thermal decomposition mass loss temperature of the liquid crystal polyarylester LCP material can be improved. The liquid crystal polyarylester contains amido bonds and forms strong interaction with hydroxyl and carboxyl on the surface of the graphene oxide, the interfacial compatibility between the graphene oxide and the liquid crystal polyarylester can be improved, the graphene oxide does not need surface modification and has good dispersity in the LCP material, a conductive path is formed, and the conductivity and the antistatic performance are improved.

The invention discloses a preparation method and application of a metal covalent organic framework material, and the prepared metal covalent organic framework material can be used for adsorption separation of elemental iodine pollutants and shows excellent iodine adsorption capacity and rate. According to the preparation method, 1H-pyrazole-4-formaldehyde and copper nitrate trihydrate are subjected to a solvothermal reaction to prepare a copper ion ring trinuclear metal complex with an aldehyde group, and the copper ion ring trinuclear metal complex and 1, 3, 5-tri (4-aminophenyl) benzene are further subjected to a Schiff base reaction to prepare the metal covalent organic framework material containing copper ions. According to the metal covalent organic framework material disclosed by the invention, copper ion active adsorption sites in a chemical structure are also retained while a developed microporous structure is maintained, and the interaction strength of pore channels to iodine is remarkably enhanced, so that the iodine adsorption rate and capacity are remarkably improved. The preparation method is simple, convenient, universal and high in controllability, and large-scale production and manufacturing of the metal covalent organic framework adsorption material can be achieved.

The invention discloses a preparation method of a hydrophobic modified copper-based monatomic catalyst. The preparation method comprises the following steps: S1, dissolving Cu (NO3) 2 and L-alanine in deionized water; dissolving trimesic acid in an ethanol solution; s2, mixing the two solutions, and stirring at regular time at normal temperature to obtain a Cu-BTC precursor; s3, grinding and uniformly mixing the Cu-BTC precursor and dicyandiamide, and then putting the mixture into a tubular furnace for high-temperature pyrolysis treatment to obtain Cu-N-C-Pre powder; s4, the Cu-N-C-Pre powder is subjected to acid leaching impurity removal treatment in an acid solution, and the copper-based monatomic catalyst is obtained; and S5, dissolving the Cu-N-C catalyst and triacetylene benzene in an organic solvent, adding pyridine, uniformly stirring, and carrying out a hydrothermal reaction to obtain the hydrophobic modified copper-based monatomic catalyst. Hydrophobic modification is performed on the surface of the Cu-N-C monatomic catalyst, so that the hydrophobicity of the surface of the catalyst is enhanced, the catalytic activity of the catalyst in a reaction for preparing phenol by activating a benzene C-H bond by taking H2O2 as an oxidizing agent is improved, and the yield of phenol is increased.

The invention provides a preparation method of an alpha-difluoroselenomethyl ketone derivative, which is a method for preparing the alpha-difluoroselenomethyl ketone derivative by using 2, 2-difluoroolefin and dialkyl diselenide in the presence of iodosobenzene diacetate. The preparation method specifically comprises the following steps: dissolving 2, 2-difluoroolefin and a dialkyl diselenide compound in an organic solvent, uniformly mixing, adding iodobenzene diacetate, and stirring and reacting at a certain temperature in an air atmosphere to obtain the product alpha-difluoro (seleno) methyl ketone derivative. The alpha-difluoroselenomethyl ketone derivative can be mildly and efficiently obtained by only adopting iodobenzene diacetate without necessary catalysts, alkali, persulfide and persulfate compounds in the prior art. Wherein R1 and R2 are aliphatic hydrocarbon, substituted and unsubstituted benzene, substituted and unsubstituted naphthalene or other aromatic groups.

The invention belongs to the technical field of epoxy resin wear-resistant coatings, and discloses a modified wear-resistant anticorrosive resin coating and a preparation method thereof. And adding a modifier into the homogeneous mother liquor, and uniformly mixing for reaction to obtain the liquid modified wear-resistant anticorrosive coating. Then standing to eliminate bubbles generated in the reaction process; and finally, curing to obtain the solid modified wear-resistant anticorrosive resin coating. According to the invention, polyphenyl-terminated hydroxyl group siloxane is used as a filler, hydroxyl is used for reacting with an epoxy group in a matrix, and homogeneous toughening is carried out to crosslink the polyphenyl-terminated hydroxyl group siloxane into a curing network of epoxy resin, so that the risk of cracking of the coating is reduced; through the synergistic effect of a rigid ring benzene ring and a flexible bond Si-O, the hardness of a paint film can be improved, the brittleness of the paint film is reduced, and the possibility that the paint film is cracked due to impact is reduced.

The invention provides an electrolyte and a lithium iron manganese phosphate battery, and relates to the technical field of lithium batteries. The electrolyte comprises a lithium salt, an organic solvent and an additive, the additive is a phenylboronic acid pinacol ester compound, and the phenylboronic acid pinacol ester compound has a structure as shown in a formula I. The electrolyte provided by the invention is helpful for improving the cycling stability of the lithium manganese iron phosphate battery under a high-temperature condition.

The application belongs to the technical field of dechlorination carrier and specifically provides a preparation method of a dechlorination active carrier, which comprises the following steps: 1) polyoxyethylene-polyoxypropylene block copolymer and modified protein solution are dissolved in deionized water, then cobalt nitrate, aluminum lactate and 2-aldehyde benzene boronic acid are added and stirred uniformly, reaction is carried out at 110-130 DEG C, centrifugation and drying are carried out to obtain a precursor; 2) tetrabutylphosphonium hydroxide and sodium aluminate are added into deionized water, TEOS and the precursor are added after mixing, stirring is carried out, crystallization is carried out at 165-175 DEG C, centrifugation and washing are carried out, and the obtained solid is dried and calcined to obtain the dechlorination active carrier. The carrier prepared by the application has the advantage of good dechlorination effect.

The invention discloses a preparation method and application of a repulpable gallic acid-based waterproof and oil-proof agent, and belongs to the technical field of bio-based oil-proof hydrophobic paper surface coatings. The preparation method comprises the following steps: by taking alkyl gallate and epoxy chloropropane as raw materials, preparing alkyl gallate epoxy through epoxidation reaction; and uniformly mixing the alkyl gallate epoxy resin with an acid anhydride / phenol compound to obtain the alkyl gallate epoxy resin series waterproof and oil-proof agent. The structure of the bio-based waterproof and oil-proof agent prepared by the invention contains groups such as a non-polar long alkyl chain, an epoxy group and an amino group, a compact cross-linked coating can be formed on the surface and the interior of paper, and gaps between paper cellulose are filled, so that permeation of oil, water and gas is blocked, meanwhile, the adhesive force between the coating and the paper is increased, and the waterproof and oil-proof effects are improved. The fibers are more tightly combined together; non-polar long alkyl chains and benzene ring groups in the structure can endow the paper with excellent oil-proof, hydrophobic and mechanical properties, and flexible chain segments (alkyl carbon chains) with different lengths are introduced to adjust the flexibility of the coating, so that the flexibility and tensile strength of the paper can be effectively adjusted; the coating paper can be recycled and reused in an alcoholysis mode. The raw materials are easy to obtain and renewable, paper can be re-pulped after being coated, and the paper has the potential of replacing plastic packaging and meets the performance requirements of paper packaging on specific scenes such as water resistance and oil resistance.

The invention discloses a 1, 4-bis (4-fluorobenzoyl) benzene production waste utilization process, which belongs to the technical field of 1, 4-bis (4-fluorobenzoyl) benzene production, and comprises the following steps: dissolving waste leftovers in a solvent, and adsorbing and removing pigments and solid particles in the leftovers by activated carbon; carrying out dehalogenation and hydrogenation on the pretreated leftovers in the presence of a hydrogenation catalyst and an alkaline substance to produce 1, 4-biphenyl acyl benzene; and carrying out separation and purification on the hydrogenation product in a solution crystallization manner to obtain 1, 4-biphenyl acyl benzene with the purity of more than or equal to 99.75%. The waste leftovers are used for producing the 1, 4-biphenyl acyl benzene, so that the utilization rate of the raw materials is increased, the discharge of hazardous wastes is reduced, and the method is green and environment-friendly.

The invention relates to the technical field of semiconductors, and provides a boron-nitrogen-containing organic compound and an organic electroluminescent device containing the same. The compound serving as a doping material has high fluorescence quantum efficiency, the rigidity of a mother nucleus structure is enhanced after a five-membered heterocycle is fused at a central benzene ring, vibration coupling is effectively inhibited, FWHM is narrowed, and the luminous efficiency of a device is improved; in addition, the rigidity of the material is enhanced, so that the evaporation decomposition temperature is increased, evaporation decomposition of the material is inhibited, and the service life of the device is effectively prolonged.

The invention provides an aqueous zinc ion battery electrolyte, a preparation method thereof and a zinc ion battery, and belongs to the technical field of aqueous zinc ion batteries. The aqueous zinc ion battery electrolyte comprises an additive, an inorganic zinc salt and a solvent, the additive comprises at least one of trimethylamine substituted by 1-3 substituent groups, benzene and C3-C10 straight-chain alkane, and the substituent groups comprise phosphonic acid groups or phosphinic acid groups; the solvent comprises a sodium chloride aqueous solution. By adopting the additive with a specific structure and the solvent containing the sodium chloride aqueous solution, the cycle performance of the zinc negative electrode in the water-based zinc ion battery can be remarkably improved, and the service life of the water-based zinc ion battery is prolonged.

The invention belongs to the technical field of high polymer materials, and relates to a modified epoxy emulsion which comprises 70-80 parts of epoxy resin, 5-7 parts of an emulsifier, 0.4-0.8 part of an initiator, 60-80 parts of a mixed monomer and 180-220 parts of water. The mixed monomer is prepared from a soft and hard acrylic monomer, acrylic acid, glycidyl methacrylate, alkenyl silane modified nano silicon dioxide and caprolactone acrylate according to a specific proportion. The invention also discloses a preparation method of the modified epoxy emulsion, and in-situ grafting of nano silicon dioxide is realized by adopting a pre-emulsion step-by-step dropwise adding process. When the emulsion is applied to the three-dimensional anti-counterfeiting temperature-sensitive ink, the emulsion has a synergistic effect with expanded microspheres grafted with amino-containing benzene rings on the surfaces: epoxy groups of glycidyl methacrylate and amino groups on the surfaces of the expanded microspheres are crosslinked to form an interpenetrating network, nano silicon dioxide is dispersed in the interpenetrating network as a rigid node, and caprolactone chain segments provide network elasticity, so that the three-dimensional anti-counterfeiting temperature-sensitive ink is prepared. Therefore, the ink has high adhesive force, excellent wear resistance and weather resistance, and is particularly suitable for printing temperature change-three-dimensional double anti-counterfeiting marks.

The invention belongs to the field of sodium-ion batteries, and discloses a sodium-ion battery electrolyte and a sodium-ion battery. The sodium-ion battery electrolyte comprises sodium salt, an organic solvent and an organic molecular additive shown in the following formula, wherein R1 to R5 are respectively and independently any one of F, Cl, Br, I, CN, H, OH, SH and NO2. A boron atom in the molecular structure of the additive is used as an electron-deficient center and can be preferentially complexed with anions or solvent molecules in the electrolyte to pre-stabilize an electrode interface; the bond energy of the B-O bond is moderate, so that the oxidation potential of the B-O bond is lower than that of a main body carbonate solvent, the B-O bond can be preferentially decomposed in the first charge-discharge process, and a thin, compact and highly stable positive electrode electrolyte interface film is formed on the surface of a positive electrode; the controllable substituent group on the benzene ring further regulates the decomposition potential of molecules through an electronic effect, so that the film forming time and the film property can be precisely regulated and controlled. The stable CEI can effectively inhibit continuous decomposition of the electrolyte at high temperature and high pressure, and the cycling stability of the battery in the high-temperature and high-pressure environment is remarkably improved.

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 relates to the technical field of epoxy resin materials, and discloses an epoxy resin material based on two-dimensional aromatic polyamide and a preparation method thereof.The preparation method comprises the specific preparation steps that firstly, melamine reacts with 1, 3, 5-trimesoyl chloride, washing, centrifuging and drying are performed to obtain two-dimensional aromatic polyamide, and the two-dimensional aromatic polyamide is ground into nano powder; secondly, adding the nano powder according to 0.5% of the mass of the amine curing agent, and performing ultrasonic dispersion to form a homogeneous-phase enhanced curing agent; and finally, blending the bisphenol A resin E51, the perfluorooctanoyl chloride modified melamine and the amine curing agent containing the two-dimensional aromatic polyamide to obtain the epoxy resin material. The two-dimensional aromatic polyamide epoxy resin material disclosed by the invention has relatively good mechanical property and waterproof property.