9469 results about "Organosolv" patented technology

The invention relates to a high-voltage-resistant deep eutectic-based in-situ polymerization solid electrolyte as well as preparation and application thereof. The in-situ polymerization solid electrolyte is obtained through an in-situ polymerization reaction of a precursor solution comprising 30-80 wt% of a deep eutectic solution, 10-50 wt% of a polymerizable monomer, 1-30 wt% of an additive and 0.05-10 wt% of an initiator; the deep eutectic solution comprises a lithium salt and a hydrogen bond donor organic solvent; the hydrogen bond donor organic solvent comprises a nitrile solvent and a non-nitrile solvent; the polymerizable monomer comprises a monomer for free radical-initiated polymerization or ring-opening polymerization; the additive comprises lithium nitrate and fluoroethylene carbonate. The high-voltage-resistant in-situ polymerization solid electrolyte formed by in-situ compounding of an organic framework formed by in-situ polymerization of a deep eutectic solution, an additive and a monomer has the excellent characteristics of wide electrochemical window, high ionic conductivity, high mechanical strength, good flame retardance, wide-temperature applicability and the like, and can be suitable for a high-voltage system of 4.6 V or above; the solid-solid contact problem of a solid-state battery interface is effectively solved, and the side reaction between the electrolyte and the lithium metal negative electrode is reduced.

The invention provides an alkaline electrolytic water hydrogen production diaphragm based on zirconium oxide modification, the alkaline electrolytic water hydrogen production diaphragm comprises a support layer and a hydrophilic modified coating on the support layer, the hydrophilic modified coating is obtained by coating the support layer with a casting liquid prepared from modified zirconium oxide particles, a film-forming polymer and an organic solvent and then carrying out non-solvent induced phase inversion, the modified zirconium oxide particles are prepared by adding micron-sized zirconium oxide and alkali liquor into a ball mill for ball milling, and the particle size of the zirconium oxide subjected to ball milling treatment is 20-100nm. According to the method, the structure of the micron-sized zirconium oxide particles is regulated and controlled by combining a ball milling-alkali etching synchronous process. Through combination of ball milling treatment and alkali etching treatment, the dispersion degree and the reaction opportunity of the zirconium oxide powder can be effectively improved, and the efficiency of the etching process is remarkably improved. The obtained modified zirconium oxide particles endow the diaphragm with excellent hydrophilicity, alkali resistance and OH <-> ion conduction performance, and the diaphragm has excellent performance when being used as an alkaline electrolytic water hydrogen production diaphragm.

The invention provides a self-repairing polyurethane film containing a disulfide bond and a DA bond and a preparation method thereof, and the preparation method comprises the following steps: (1) adding an organic solvent into a three-necked flask, then dissolving dihydric alcohol, diisocyanate, a disulfide bond monomer and a DA bond forming monomer in the organic solvent, then adding a catalyst, and mechanically stirring uniformly; (2) introducing nitrogen into the three-necked flask to evacuate air, setting a reaction temperature, and carrying out a reaction under mechanical stirring; (3) in a nitrogen environment, dropwise adding a monomer II forming a DA bond into the solution obtained after the reaction in the step (2), and after the dropwise addition of the monomer II forming the DA bond is completed, setting the reaction temperature and reacting for a period of time; and (4) pouring the solution obtained after the reaction in the step (3) into a polytetrafluoroethylene mold, and drying to obtain the self-repairing polyurethane film. The self-repairing polyurethane film prepared by the preparation method disclosed by the invention has relatively good mechanical properties, relatively good self-repairing performance under mild conditions and high self-repairing efficiency.

The invention discloses a preparation method of an ultrahigh-reflectivity radiation refrigeration fiber membrane, which comprises the following steps: dissolving a polymer in an organic solvent to prepare an electrostatic spinning precursor solution, and adjusting parameters such as the concentration of the electrostatic spinning precursor solution, spinning voltage, spinning distance, roller rotating speed, liquid supply rate, slide rail reciprocating rate and the like to prepare the ultrahigh-reflectivity radiation refrigeration fiber membrane. And preparing the ultrahigh-reflectivity radiation refrigeration fiber membrane with a porous structure, wherein the reflectivity of the ultrahigh-reflectivity radiation refrigeration fiber membrane is greater than 95% at the sunlight wave band of 0.3-2.5 microns. In the dissolving process of the polymer in the organic solvent, the water bath stirring temperature is 20-60 DEG C, the stirring time is 3-6 hours, a bilateral multi-nozzle opposite layout is adopted in electrostatic spinning, the spinning distance is 15-30 cm, the electrostatic spinning voltage is 20-50 kV, the rotating speed of a roller is 400-1000 r / min, the spinning liquid supply rate is 8-30 ml / h, the reciprocating rate of a sliding rail is 3-10 mm / s, and the thickness of the ultrahigh-reflectivity radiation refrigeration fiber membrane is 300-500 microns. The radiation refrigeration film prepared through the method can be prepared in batches, has good flexibility and can be widely applied to the fields of clothes, buildings, equipment and the like.

The invention relates to the technical field of lithium-sulfur batteries, and discloses a sulfonyl ZIF-8 metal organic framework material, a lithium-sulfur battery diaphragm and a preparation method of the lithium-sulfur battery diaphragm. The preparation method of the sulfonyl ZIF-8 metal organic framework material comprises the following steps: dissolving a metal precursor and a mixed ligand in an organic solvent, and carrying out a coordination reaction under the action of organic alkali; solid is collected, washed and dried, and the sulfonic group ZIF-8 metal organic framework material is obtained. The metal precursor is soluble zinc salt; the mixed ligand comprises 2-methylimidazole and an imidazole derivative containing a sulfonic acid group. The sulfo group ZIF-8 metal organic framework material is prepared through a ligand doping strategy and is used for functional modification of the lithium-sulfur battery diaphragm; the shuttle behavior of lithium polysulfide (LiPS) can be effectively inhibited through the electrostatic repulsion effect of sulfonic acid groups and the synergistic effect of high-polarity adsorption sites; and the migration of Li < + > and the conversion efficiency of LiPS are remarkably promoted by an efficient ion transmission network, so that the cycle performance of the lithium-sulfur battery is improved.

The invention discloses a polyimidazolone compound as well as a preparation method and application thereof. The preparation method comprises the following steps: dissolving a bilateral alkyne ester compound, amidine hydrochloride, a catalyst and a desalting agent in an organic solvent, and carrying out polymerization reaction to obtain the polyimidazolone compound. The polyimidazolone compound with the five-membered ring is selectively generated, and the method has the advantages that monomers are easy to obtain, operation is easy, and by-products are low in toxicity. The polyimidazolone compound prepared by the invention has better machinability and has potential application value in the aspects of metal ion detection and biogenic amine detection.

The invention discloses a composite electrode material for a zinc-bromine flow battery and a preparation method and application thereof, and the preparation method comprises the following steps: S1, uniformly stirring a copper salt, a zinc salt, a sodium salt and distilled water at room temperature, aging in air, and then filtering, washing and drying to obtain a zinc-copper composite salt; s2, adding a polymer into an organic solvent under a stirring condition, and stirring under a water bath condition to obtain a spinning solution; then adding zinc-copper composite salt, stirring and then carrying out ultrasonic dispersion to obtain a composite spinning solution; s3, preparing the composite spinning solution into a precursor nanofiber material by utilizing high-voltage electrostatic spinning; and S4, carrying out pre-oxidation and carbonization treatment on the precursor nanofiber material in an atmosphere furnace, and cleaning and drying the carbonized material to obtain the composite electrode material for the zinc-bromine flow battery. According to the invention, the problems of low surface activity of bromine electrode reaction on an electrode material, unstable electro-catalytic performance, bromine permeation and the like in the zinc-bromine flow battery can be solved.

The invention relates to a waterborne polyurethane sizing agent, a preparation method thereof and a carbon fiber, and belongs to the technical field of carbon fiber preparation. The preparation method of the waterborne polyurethane sizing agent comprises the following steps: S10, dispersing and mixing amino modified polydimethylsiloxane and graphene oxide in an organic solvent, carrying out grafting reaction, and carrying out vacuum drying to obtain amino modified polydimethylsiloxane grafted graphene oxide; s20, mixing polyether glycol, diisocyanate and a hydrophilic chain extender, and carrying out a first reaction to obtain a first reaction solution; mixing the first reaction liquid, a small molecule chain extender and amino modified polydimethylsiloxane grafted graphene oxide for second reaction to obtain a polymerization system; and carrying out a neutralization reaction on the polymerization system and a neutralizer, and dispersing in water to obtain the waterborne polyurethane sizing agent. The waterborne polyurethane sizing agent can effectively increase the surface roughness of carbon fibers and improve the interfacial shear strength between the carbon fibers and a resin matrix.

The invention discloses a copper-clad plate for a printed circuit board and a preparation method of the copper-clad plate, and relates to the technical field of printed circuit board materials. The invention discloses a preparation method of a copper-clad plate for a printed circuit board, which comprises the following steps of: soaking a reinforcing material in a glue solution, and drying to obtain a prepreg; carrying out hot-pressing treatment on the prepreg and copper foil to obtain a copper-clad plate; the glue solution comprises the following raw materials in parts by weight: 15-20 parts of vinyl-terminated polyphenyl ether, 20-25 parts of epoxy resin, 20-25 parts of difunctional silicon dioxide, 15-25 parts of an organic solvent, 0.3-0.6 part of a curing agent and 0.05-0.1 part of a curing accelerator; the difunctional silicon dioxide cross-linked polyphenyl ether and epoxy resin prepared by the preparation method disclosed by the invention are used as a resin material of a glue solution, and have the characteristics of good heat resistance and excellent mechanical properties.

The invention discloses a bio-based polyurethane coating and a preparation method thereof, and belongs to the technical field of coatings. The bio-based polyurethane coating comprises the following raw materials in parts by weight: 100 parts of vegetable oil polyol, 70-120 parts of isocyanate, 10-25 parts of a flame retardant, 30-40 parts of an organic solvent, 1-5 parts of a catalyst, 10-30 parts of a hydrophilic chain extender, 10-30 parts of a neutralizer and 20-40 parts of deionized water. The preparation method comprises the following steps: adding plant polyol, isocyanate, a flame retardant, an organic solvent and a catalyst into a container, mixing and reacting to obtain a prepolymer mixed solution, then adding a hydrophilic chain extender, mixing and reacting to obtain a polymer mixed solution, cooling, then adding a neutralizer for neutralizing, then adding deionized water for emulsifying to form a polyurethane emulsion, and finally adding a curing agent for curing. And performing reduced pressure distillation to obtain the bio-based polyurethane coating. According to the invention, biomass-sourced acid reacts with the organosilicon compound to generate the flame retardant, and the prepared bio-based polyurethane coating has good flame retardant property.

The invention belongs to the technical field of fiber materials, and relates to a micro-gear-shaped special-shaped stretchable conductive anti-radiation fiber and preparation and application thereof, a core layer spinning solution and a shell layer spinning solution are subjected to coaxial wet spinning to prepare the micro-gear-shaped special-shaped stretchable conductive anti-radiation fiber; the core layer spinning solution is obtained by dissolving TPU in anti-radiation particles I / anti-radiation particles II / organic solvent dispersion, and the shell layer spinning solution is obtained by dissolving TPU in MXene / organic solvent dispersion; the mass volume ratio of the TPU to the organic solvent in the core layer spinning solution is (2.2-3g): 10ml, and the mass volume ratio of the TPU to the organic solvent in the shell layer spinning solution is (0.5-1g): 10ml; the anti-radiation fiber is of a core-shell structure, the cross section of a core layer is circular, the cross section of a shell layer is of a micro-gear-shaped special-shaped structure, and the average height of gear protrusions is 20-50 m; when being applied, the fabric is processed into a stretchable multifunctional fabric by adopting a weaving process. According to the method, a coaxial wet spinning process is adopted to prepare the product in one step; the product has high sensitivity and a wide sensing range; the application range is wide.

The invention discloses a synthesis method of amphiphilic quantum dots and application of the amphiphilic quantum dots in nano oil displacement, and belongs to the field of nano oil displacement. The synthesis method comprises the following steps: heating a mixture containing a carbon source and a nitrogen source in an air atmosphere for reaction, and centrifuging, filtering and drying a reaction product to obtain the amphiphilic quantum dots, the carbon source is selected from at least one of glucose, mannose, citric acid, lignin, chitosan and starch; the nitrogen source is selected from at least one of alkylamine, and the carbon chain length of the alkylamine is C6 to C12. The synthesis method is simple, heating of a high-pressure reaction kettle is not needed, the technological process is simple, and the method is suitable for large-scale industrial production; the series of amphiphilic carbon quantum dots show better solubility and higher absolute fluorescence quantum yield in water and various organic solvents.

The invention discloses a preparation method and application of a conjugated microporous polymer microsphere filler with a hollow structure, silicon dioxide nanospheres are placed in an organic solvent, after uniform ultrasonic dispersion, 1, 3, 5-triacetylene benzene and 2, 6-dibromo-3-aminopyridine are added, after a catalyst is added, a stirring reaction is carried out in a nitrogen atmosphere to obtain yellow powder, and the yellow powder is dried to obtain the conjugated microporous polymer microsphere filler with the hollow structure. Etching with hydrofluoric acid, cleaning the treated product until the filtrate is transparent and colorless, and drying in vacuum to obtain the conjugated microporous polymer microsphere filler with the hollow structure. Nanoscale holes are formed in the hollow-structure conjugated microporous polymer microsphere filler, so that the hollow-structure conjugated microporous polymer microsphere filler has good heat insulation performance and good heat stability at high temperature, and can be used as a heat-resistant performance enhancing filler.

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 present disclosure provides a solid electrolyte composition that can suppress deterioration in ion conductivity of an ionic solid electrolyte material. The solid electrolyte composition according to the present disclosure contains a sulfur element-free ionic solid electrolyte material and an organic solvent, where the organic solvent includes at least one selected from the group consisting of a hydrocarbon and a compound having a functional group; and the functional group is at least one selected from the group consisting of an ether group, a halogen group, and a Si—O—C group.

The invention belongs to the technical field of organic pollution treatment, and relates to a biochar-LDH-nZVI-GO composite material for organic pollution remediation and a preparation method and application thereof.The preparation method comprises the steps that graphene oxide is ultrasonically dispersed in deionized water, magnesium salt and aluminum salt are added to form uniform suspension liquid, then the uniform suspension liquid is mixed with biochar suspension liquid, and the biochar-nZVI-GO composite material is obtained; carrying out pH (Potential of Hydrogen) regulation and a hydrothermal crystallization reaction, so as to prepare a biochar-Mg / Al-LDH-GO compound; and dispersing the compound in an organic solvent, sequentially adding FeSO4. 7H2O and a NaBH4 solution in an inert atmosphere to carry out a reduction reaction, and finally washing and drying to obtain the biochar-LDH-nZVI-GO composite material. The material shows high-efficiency removal capacity on various organic pollutants such as trichloroethylene, chlorobenzene and polychlorinated biphenyl, is suitable for high-efficiency green remediation of organic pollutants in soil and water, and has good popularization and application prospects.

The invention provides a sodium ion battery, an energy storage device and an energy storage system. The sodium ion battery comprises a positive pole piece, a diaphragm, a negative pole piece and an electrolyte, the negative pole piece comprises a carbon material, the specific surface area of the carbon material is x, the carbon material comprises mesopores, the number percentage of the mesopores in the carbon material is y, and the electrolyte comprises an organic solvent, an electrolyte salt, an organic additive and a sodium salt additive, the organic solvent comprises cyclic carbonate and chain carbonate, the mass fraction of the cyclic carbonate in the electrolyte is a, the mass fraction of the chain carbonate in the electrolyte is b, the mass fraction of the organic additive in the electrolyte is c, and the mass fraction of the sodium salt additive in the electrolyte is d; the sodium ion battery meets the relational expression of 0.4 < = a / y < = 0.8; 0.5 < = a / b < = 1.3; 0.4 < = c / x < = 1.2; and 0.1 < = d / c < = 0.5.

The present disclosure provides a solid electrolyte composition that can suppress deterioration in ion conductivity of an ionic solid electrolyte material. The solid electrolyte composition according to the present disclosure contains a sulfur element-free ionic solid electrolyte material and an organic solvent, where the organic solvent includes at least one selected from the group consisting of a hydrocarbon and a compound having a functional group; and the functional group is at least one selected from the group consisting of an ether group, a halogen group, and a Si—O—C group.

The invention relates to the technical field of biological extraction, in particular to a green synergistic extraction system and an extraction method and application thereof.The green synergistic extraction system comprises a deep eutectic solvent system, an enzymolysis system and an ultrasonic-assisted extraction system, and the deep eutectic solvent system comprises a DES solvent; the DES solvent is composed of a hydrogen bond acceptor and a hydrogen bond donor, and the hydrogen bond acceptor is choline, choline chloride or L-proline; the hydrogen bond donor is lactic acid, urea or ethylene glycol; enzyme preparations in the enzymolysis system are at least two of cellulase, pectinase and beta-glucosidase; the problems that a traditional organic solvent is high in toxicity and poor in biodegradability and synthetic deep eutectic solvent raw materials are non-renewable are solved, a green synergistic extraction system which is environmentally friendly, low in cost and excellent in performance is developed, the mass transfer efficiency and the extraction yield are improved, the used DES and enzyme preparations can be recycled, and the cost is reduced while the environment is protected.

The invention relates to the technical field of drilling fluid cooling, and discloses a phase change microcapsule suitable for drilling fluid cooling and a preparation method thereof.The phase change microcapsule comprises a capsule wall stabilizing material and a capsule core phase change material, and the capsule wall stabilizing material comprises polyurethane, polyurea, polyamide, polyimide, polystyrene and a first organic solvent; the capsule core phase change material comprises paraffin, fatty acid, polyol, inorganic hydrated salt, polymer gel, expanded graphite, carbon nanotubes, metal nanoparticles and a second organic solvent, and the first organic solvent is at least one of toluene, xylene, cyclohexanone and the like. The temperature of the drilling fluid is kept at a relatively low level, the cooling of the drilling fluid is realized, so that the drilling efficiency is improved, harmful solvents and additives are not used in the preparation process of the phase-change microcapsules, the phase-change microcapsules are pollution-free to the environment, and the requirements of greenness and environmental protection are met.

The invention relates to an in-situ polymerized flame-retardant perfluorogel electrolyte, a lithium metal battery and a preparation method, the in-situ polymerized flame-retardant perfluorogel electrolyte is prepared from a fluorinated organic solvent, a lithium salt, a fluorine-containing polymer precursor and a thermal initiator, and the fluorine-containing polymer precursor further comprises a fluorine-containing polymer and a cross-linking agent. Compared with the prior art, the composite material has a high electrochemical window and excellent flame retardant property, and can realize matching with a high-voltage high-nickel positive electrode at room temperature and stable circulation of a high-voltage lithium metal battery; the preparation method is simple, the interface performance is optimized, and large-scale preparation is easy to realize.

The present application belongs to the field of polymer material technology, and in particular, relates to a polyimide composite material, a preparation method thereof, and an application thereof. The preparation method of the polyimide composite material comprises the steps of: preparing a polyamic acid slurry from a diamine monomer, a dianhydride monomer, and an organic solvent; preparing a mixed slurry from the polyamic acid slurry and a nanomaterial, and then performing a spinning imidization treatment to obtain a polyimide composite material; wherein the nanomaterial comprises at least one of nano silicon carbide, aluminum nitride, carbon nanotubes, graphene, and nano silicon dioxide. By blending polyimide with other nanomaterials having high thermal conductivity to improve its thermal conductivity, the thermal conductivity of the polyimide composite material is optimized and improved, and its heat dissipation capacity in a high temperature working environment is enhanced, while having high tensile strength and thermal conductivity. The service life of the polyimide composite material is extended, and its application range can be further expanded, such as in the back panel assembly of a smartphone.

The invention discloses a phthalonitrile modified phenolic aerogel and a preparation method and application thereof. Linear phenolic aldehyde, 4-nitrophthalonitrile and a basic catalyst are dissolved in an organic solvent, a water bath reaction is conducted, powder is prepared, and phthalonitrile etherified phenolic resin is obtained; preparing a mixed solvent, and dissolving linear phenolic aldehyde and phthalonitrile etherified phenolic resin in the mixed solvent to obtain a mixed solution; adding a cross-linking agent into the mixed solution, carrying out sol-gel reaction to obtain wet gel, and aging, segmentally curing and drying the wet gel to obtain the phthalonitrile modified phenolic aerogel. The pyrolytic property of the phenolic aerogel is improved, the phthalonitrile modified phenolic aerogel with high carbon residue and high thermal stability is obtained under the condition of low-temperature heating, and the method is suitable for being applied to the field of thermal insulation ablation of a thermal protection system of aerospace equipment.

The invention provides gel with a three-dimensional network structure, a preparation method of the gel and a lithium battery, and belongs to the technical field of lithium batteries. The gel provided by the invention comprises the following raw materials: polyethylene glycol dimethacrylate (PEGDMA) and / or a derivative thereof, a fluorine-containing carbonate compound, a cross-linking agent, a lithium salt, a flame retardant and an organic solvent. The PEGDMA and / or the derivative thereof and the fluorine-containing carbonic ester compound generate a three-dimensional network structure under the action of the cross-linking agent, the fluorine-containing carbonic ester compound can improve the interface stability between the gel and the electrode material, reduce the interface side reaction and improve the thermal stability of the gel, and the performance of the electrode material is improved. Meanwhile, the three-dimensional network structure has relatively high porosity and liquid absorption capacity, so that an ion transmission channel is improved, and the ionic conductivity of the gel is further improved. The room-temperature ionic conductivity of the gel with the three-dimensional network structure is larger than or equal to 3 mS / cm, and the thermal decomposition initial temperature is larger than or equal to 250 DEG C.

The invention discloses a method for purifying electronic-grade hafnium tetrachloride, which comprises the following steps of: removing insoluble substances by adopting an organic solvent matched with hafnium tetrachloride, removing low-melting-point impurities through low-temperature boiling, removing high-melting-point impurities through high-temperature sublimation, and removing substances with different chemical properties and polarities through a complexing and decomplexing method. And finally, sublimating to further remove impurities to finally obtain the electronic-grade hafnium tetrachloride with the purity not lower than 7N grade. The method has the characteristics of good purification effect, multi-method comprehensive impurity removal, industrial large-scale application, stable quality, high yield and simple and easy-to-separate impurity components.

The invention discloses a preparation method and application of a carbon dioxide gas capture functional molecule modified nanogold catalyst. The preparation method comprises the following steps: synthesizing a modified molecule with a carbon dioxide gas capturing function through a chemical reaction; adding the modified molecules into an organic solvent, and uniformly mixing to obtain a solution; then adding a nanogold colloidal solution into the solution, uniformly stirring, and carrying out oil bath heating reaction; and after the reaction is completed, cooling to room temperature, carrying out suction filtration on the reaction liquid, respectively washing with ethanol and deionized water, and carrying out vacuum drying on the product to obtain the carbon dioxide gas capture functional molecule modified nanogold catalyst. In the electrocatalytic carbon dioxide reduction reaction process of the obtained catalyst, modification molecules are connected with the nanogold catalyst through chemical bonds, active sites of the nanogold catalyst are exposed, and meanwhile, an interface environment beneficial to the carbon dioxide reduction reaction can be provided; therefore, high activity, high selectivity and high stability of the molecular modified nanogold catalyst are realized.

The invention provides a non-aqueous electrolyte, a lithium ion battery, a battery module, a battery pack and a power utilization device, the non-aqueous electrolyte comprises a lithium salt, an organic solvent and an electrolyte additive, and the electrolyte additive comprises 1, 3-propane sultone, fluoroethylene carbonate, vinylene carbonate, lithium tetrafluoroborate and a compound I shown in the formula I. The non-aqueous electrolyte is applied to the lithium ion battery, and the cycle life of the lithium ion battery is prolonged.

The invention belongs to the technical field of water electrolysis hydrogen production diaphragms, and relates to coating slurry for a composite diaphragm in an alkaline electrolytic cell and a preparation method of the coating slurry. The coating slurry comprises a high-molecular polymer, an inorganic hydrophilic oxide, a polymer electrolyte, a pore-foaming agent and an organic solvent. The high-molecular polymer is polysulfone, and the inorganic hydrophilic oxide is titanium dioxide; and the polymer electrolyte is acacia gum. And the pore-foaming agent is polyvinylpyrrolidone. Titanium dioxide is used as a filler, so that the hydrophilicity of the hydrophobic polysulfone membrane can be improved, and the transfer of hydroxyl ions is facilitated. Hydroxyl, amino and other hydrophilic groups of the acacia gum are migrated to a membrane-water interface, and the groups and a membrane matrix are combined to form a hydrogen bond network, so that the stability and the water adsorption capacity of the membrane are enhanced, and the composite membrane with low surface resistance, smooth surface, compact coating and good mechanical capacity is obtained. The nylon and the acacia gum are adopted, cost is low, and large-scale production is facilitated.

The invention discloses a method for preparing hydrophobic SiO2 aerogel through in-situ polymerization. The method comprises the following steps: (1) uniformly mixing and stirring an alcohol solvent, a silicon source, water, an in-situ modifier and a catalyst to obtain a mixed solution; (2) adding an acid adjusting solution into the obtained mixed sol solution to hydrolyze the mixed sol solution, and adding an alkali adjusting solution to polymerize the mixed sol solution; (3) gum dipping: dipping the silica sol solution into the inorganic fiber material through a gum dipping process to obtain a compound of the silica sol and the inorganic fiber material, and standing to obtain a gel composite material; (4) aging: adding the obtained composite gel material into an aging liquid mixed solution; and (5) immersing the aged wet gel in an organic solvent, and then feeding into a supercritical drying kettle for supercritical drying treatment to obtain the SiO2 aerogel composite material. By adopting an in-situ polymerization method, the use of a hydrophobic modifier is reduced, the aerogel preparation process period is shortened, and the production process is simple.

The invention relates to curcumin-loaded pectin sodium alginate gel as well as a preparation method and application thereof, and belongs to the technical field of gel preparation. The preparation method of the curcumin-loaded pectin sodium alginate gel comprises the following steps: in a dark environment, stirring and mixing curcumin, arjunic acid, ortho-aminophenol and an organic solvent, adding a polyvinyl alcohol aqueous solution, a sodium alginate solution and a pectin solution, uniformly mixing, performing ultrasonic treatment, adding calcium chloride, stirring and mixing, performing ultrasonic treatment, and performing vacuum drying to obtain the curcumin-loaded pectin sodium alginate gel. And adding oxidized hyaluronic acid, continuously stirring, stirring at normal temperature until the organic solvent is completely volatilized, and cleaning the hydrogel with deionized water to obtain the hydrogel. According to the invention, calcium ions and sodium alginate are subjected to physical crosslinking, pectin and polyvinyl alcohol are combined to form a composite hydrogel layer, the compounding of multiple components can effectively control the dissolution and drug release behaviors of active components, the bioavailability of curcumin is increased, the compactness and stability of hydrogel are increased, and the bioavailability of curcumin is improved. The oxidation resistance of the hydrogel can be effectively improved.