1019 results about "Hexane" patented technology

The invention belongs to the technical field of insulator materials, and particularly relates to an insulating busbar and a preparation method thereof. The preparation method of the insulating busbar comprises the following steps: coating glue on the surface of a busbar base material, and drying to obtain a busbar with a bonding layer; the preparation method comprises the following steps: mixing 40 to 60 parts of silicon resin, 20 to 40 parts of grafted silicon dioxide, 10 to 20 parts of aluminum oxide and 2 to 4 parts of 2, 5-dimethyl-2, 5-bis-(tert-butylperoxy) hexane, so as to obtain a sizing material; placing the busbar with the bonding layer in a mold, then adding a sizing material, and pressing to obtain an insulating busbar; the preparation method of the grafted silicon dioxide comprises the following steps: stirring m-aminobenzoic acid and 3-aminopropyltriethoxysilane for reaction to obtain a grafting solution, and adding silicon dioxide into the grafting solution for grafting reaction to obtain the grafted silicon dioxide.

This disclosure relates to the fabrication of high-performance thin film composite (TFC) reverse osmosis (RO) membranes comprising a thin polyamide rejection layer (thickness of 100-200 nanometer), a porous substrate including polysulfone (PSf) layer (thickness of 40-50 micron) cast on polyester nonwoven fabric (thickness of ˜100 micron). Hydrophilic and antibacterial TFC polyamide RO membranes were developed by incorporating green Lignin and nanostructured silver-based metal organic frameworks (MOFs) into the selective layer. The polyamide layer of TFC RO membranes was fabricated on the porous PSf substrate by interfacial polymerization between aqueous monomer solutions containing MPD, and adequate additives in water and organic monomer solutions containing TMC in the mixture of hexane and co-solvents. The optimized produced RO membranes were provided water flux of 95-100 LMH and sodium chloride (NaCl) salt rejection of 98.5-99.0% during filtration of 2000 ppm NaCl solution at 225 psi pressure, and water flux of 55-60 LMH and sodium chloride (NaCl) salt rejection of 98.6-98.9% during filtration of 35000 ppm NaCl solution at 800 psi pressure. This disclosure also relates to developing a roll-to-roll PSf membrane as a substrate for making TFC RO membranes for water desalination

The invention discloses a preparation method of EVOH, and relates to the technical field of EVOH. According to the method, a low-temperature (0-5 DEG C) methanol-n-hexane mixed solvent system is creatively adopted and matched with a penetration enhancer to realize synergistic extraction, so that synchronous and deep removal of polar and non-polar small molecular impurities in the EVA is finally realized, the content of impurities in the EVA is remarkably reduced, and the self-polymerization reaction of residual monomers is effectively inhibited; therefore, a key guarantee is provided for subsequent preparation of high-quality EVOH products. The film processed by the EVOH prepared by the invention has the characteristics of few crystal points and high product quality, and can be applied to the field of high-barrier packaging film materials.

The invention relates to the technical field of membrane separation, in particular to a preparation method of a pH-step-by-step thermocuring regulation sodium-magnesium separation nanofiltration membrane. The method comprises the following steps: (1) pre-treating a base membrane; (2) preparation and treatment of an aqueous phase solution: S1, preparing the aqueous phase solution according to mass fraction: sequentially adding 1.2%-1.6% of piperazine, 0.10%-0.14% of triaminopyrimidine and 0.14%-0.18% of polyethylene glycol into deionized water, and stirring until the piperazine, the triaminopyrimidine and the polyethylene glycol are completely dissolved to form the aqueous phase solution; s2, adjusting the pH value of the water-phase solution to 10-11 by using hydrochloric acid; s3, pouring the water-phase solution of which the pH is adjusted on the surface of the pretreated base membrane, standing, and blow-drying to form a uniform water-phase layer; (3) interfacial polymerization reaction: S1, preparing an oil phase solution: adding 0.10-0.14% of trimesoyl chloride into n-hexane, and performing ultrasonic treatment until the trimesoyl chloride is completely dissolved; s2, pouring the oil-phase solution on the surface of the base membrane subjected to water-phase treatment, and after reaction, pouring out redundant solution to form a polyamide separation layer, so as to obtain a membrane sheet; (4) performing a step-by-step thermocuring process; and (5) cleaning and storing.

The invention relates to the field of pharmaceutical analytical chemistry, in particular to a method for determining tandospirone and salt intermediates thereof, high performance liquid chromatography is adopted, and chromatographic conditions include that a chromatographic column with octadecylsilane chemically bonded silica as a filler is adopted, and gradient elution is performed by a mobile phase A and a mobile phase B; wherein the mobile phase A consists of a first water phase and acetonitrile; the mobile phase B is composed of a second water phase and acetonitrile; the first water phase is a water solution containing monopotassium phosphate and sodium hexanesulfonate, and the pH value of the first water phase is 3.0-3.8; the second water phase is an aqueous solution containing monopotassium phosphate and sodium hexanesulfonate, and the pH value of the second water phase is 1.8-2.6. The testing method disclosed by the invention has good specificity, accuracy and repeatability, and can be used for monitoring the quality of the tandospirone raw material medicine.

The invention provides a preparation method of a high-flux stable-selection anti-fouling nanofiltration membrane, which comprises the following steps: carrying out amination modification on a nano material by an activation method to prepare a modified nano material; piperazine, an acid absorbent and the modified nano material are added into deionized water to be mixed, and a water phase solution is prepared; the preparation method comprises the following steps: mixing trimesoyl chloride and normal hexane to prepare an organic phase solution; immersing the polyethersulfone-based membrane into the water phase solution, draining, inversely immersing into the organic phase solution, and carrying out interfacial polymerization reaction to generate a polyamide layer to obtain a composite membrane; and then carrying out post-treatment on the composite membrane to obtain the composite membrane. The membrane has high permeability, high selectivity and strong anti-pollution performance.

The invention provides a hole transport layer precursor solution, a hole transport layer, a preparation method and application of the hole transport layer, and a perovskite cell, and belongs to the technical field of hole transport layers. The hole transport layer precursor solution comprises a self-assembled single molecule and an organic solvent; the organic solvent comprises a solvent A, a solvent B and a solvent C; the solvent A comprises more than one of a phosphate ester solvent and an alcohol ether solvent; the solvent A contains four hydrogen bond receptors; the boiling point of the solvent A is 215-290 DEG C; the solvent B comprises more than one of ethanol, isopropanol, normal propyl alcohol, butanol, ethylene glycol and N, N-dimethylformamide; the solvent C comprises more than one of ethyl acetate and normal hexane. A ternary hydrogen bond network is formed through the solvent A, the solvent B and the solvent C, the agglomeration degree of SAM molecules is remarkably reduced, and the device performance is improved.

The invention relates to the technical field of repair materials, and particularly discloses an extracellular matrix fiber material as well as a preparation method and application thereof. The invention discloses a preparation method of an extracellular matrix fiber material. The preparation method comprises the following steps: taking animal tissues, and carrying out virus inactivation, decellularization and antigen removal, degreasing, drying, grinding and sterilization; the decellularization and antigen removal method comprises the following specific steps: sequentially soaking a sample with a surfactant solution for h; then, soaking treatment is carried out by adopting a salt-alkali solution which contains 0.05-3 mol / L of salt and has the pH value of 8-11; then carrying out soaking treatment by adopting a 0.1-1wt% enzyme solution; and in degreasing, one or more of normal hexane, trichloromethane, dichloromethane, methanol, ethanol, acetone, diethyl ether and ethyl acetate are used for soaking the sample. According to the technical scheme, the ECM powder particle material with high growth factor content is prepared.

The invention relates to the technical field of all-solid-state batteries, in particular to air-stable argyrodite type sulfide electrolyte, a preparation method thereof and an all-solid-state battery. The air-stable argyrodite type sulfide electrolyte provided by the invention comprises a sulfide solid electrolyte and a protective layer formed by self-assembly of organic molecules on the surface of the sulfide solid electrolyte, wherein the sulfide solid electrolyte is argyrodite type sulfide solid electrolyte, the general formula of the sulfide solid electrolyte is Li < 7-a > PS < 6-a > X , X is halogen, and a is more than 0 and less than 2; the organic molecule is at least one of 1-methoxyhexane, 2-heptanone, 3-chloropropanol, 4-chlorobenzyl mercaptan, n-amylamine, 5-chloromethyl-1, 3-benzodioxole, chlorophenylmethane and ethylbenzene, and the organic molecule is at least one of 1-methoxyhexane, 2-heptanone, 3-chloropropanol, 4-chlorobenzyl mercaptan, n-amylamine, 5-chloromethyl-1, 3-benzodioxole, chlorophenylmethane and ethylbenzene. According to the air-stable argyrodite type sulfide electrolyte provided by the invention, the stability of the sulfide electrolyte to water can be enhanced, and the ionic conductivity of the sulfide electrolyte can be ensured.

The application discloses a preparation method of carbon aerogel material for light electromagnetic shielding, and comprises the following steps: adding resorcinol, phloroglucinol, a template agent and formaldehyde into pure water, stirring and dissolving to obtain a precursor solution; adding the precursor solution into white oil containing a surfactant, emulsifying, heating in an oil bath and fully reacting; centrifugal separation to obtain powder, high-temperature carbonization, dispersion in oleylamine, addition into a stock solution containing nickel acetylacetonate, triphenylphosphine and oleylamine, high-temperature reaction and cooling, addition of a mixture of hexane and ethanol to obtain a product; centrifugal separation and washing to obtain light high-electromagnetic-shielding carbon aerogel. The carbon aerogel material for light electromagnetic shielding prepared by the method has the advantages of small density, high efficiency, corrosion resistance, high electromagnetic shielding efficiency, high product yield and the like, and by controlling the nucleation and growth rate of Ni2P, the Ni2P nanoparticles can be uniformly grown on the carbon aerogel microspheres, and the method is suitable for application in large-scale industrial production.

A TPC-OTBS n-hexane solution is added to a mixture of TPC-OSO2F, DMF, and DBU and allowed to stand to produce a crosslinked solvent gel; the crosslinked solvent gel is added to methanol, stirred, and dried to produce the porous crosslinked material. The gel acquired can be prepared into a pore-rich solid porous organic polymer material by means of solvent exchange. SEM and TEM are used to characterize the surface and internal morphologies of the solid material, and the porous morphology thereof is discovered, with large pores being the majority. Infrared and nuclear magnetic resonance are used to characterize the structure of a crosslinked polysulfate; the complete reaction of a sulfuryl fluoride group is proven by means of solid-state fluorine nuclear magnetic resonance spectroscopy and XPS element analysis; and the porous structure of the crosslinked polysulfate allows same to be provided with improved application prospect in terms of adsorption.

The application discloses a preparation method of a hydrophilic oil-water separation anti-pollution membrane and the anti-pollution membrane and application thereof, and prepares MNRs material; the MNRs material is dispersed in dimethylacetamide, is uniformly stirred, polyvinylpyrrolidone is added, and stirring is continued, and a first mixture is obtained through ultrasonic treatment; the first mixture is mixed with polyvinylidene fluoride to obtain a second mixture, and the second mixture is stirred; the treated second mixture is dip-coated on a carrier, the dip-coated carrier is treated in deionized water to obtain an ultrafiltration membrane; the ultrafiltration membrane is soaked in a tea polyphenol solution with a Tris-HCl buffer solution, and is shaken to obtain the hydrophilic oil-water separation anti-pollution membrane. The hydrophilic oil-water separation anti-pollution membrane has excellent separation efficiency and flux recovery rate for four different oil-water mixtures of kerosene, gasoline, edible oil and n-hexane. The preparation process of the oil-water separation membrane is simple, the cost is low, and the reaction condition is mild; when the oil-water separation membrane is applied to organic wastewater separation, the oil-water separation membrane has the advantages of high efficiency, good removal performance and good recycling performance.

The application discloses a preparation method of a catalyst for liquid-phase refining of crude octanol, and the preparation method comprises the following steps: (1) mixing pretreated fly ash and pseudo-boehmite, adding deionized water and nitric acid, stirring until a colloid is formed, drying the colloid, mixing the dried colloid with kaolin, and obtaining a carrier through kneading, extrusion molding, drying and calcination; (2) taking a nickel salt, a manganese salt and a zinc salt as active components, taking a calcium salt as an auxiliary component, dissolving the active components and the auxiliary component in deionized water to obtain a salt solution, adding n-hexane into the salt solution and stirring uniformly to prepare an impregnation solution, immersing the carrier in the impregnation solution, and obtaining the catalyst through washing, drying and calcination. The catalyst prepared by the method is mainly used in a liquid-phase refining reaction process of crude octanol, and has high activity stability and selectivity.

The invention discloses a method for detecting 18 phthalic acid ester substances in brewed sauce, which specifically comprises the following steps: step 1, obtaining a sample of the brewed sauce to be detected, adding a phthalic acid ester substance internal standard working solution containing deuterated isotope and water, uniformly mixing, adding sodium chloride and acetonitrile, continuously uniformly mixing, and detecting the content of the phthalic acid ester substances in the brewed sauce to be detected; carrying out ultrasonic extraction treatment for 5-15 minutes, adding an ultrasonic extracting solution into a mixture of PSA, C18 and MgSO4, and carrying out centrifugal treatment to obtain supernate; 2, carrying out nitrogen blowing on the supernate until the supernate is nearly dry, and fixing the volume by using normal hexane to obtain a sample to be detected; and step 3, detecting by adopting a gas chromatography-tandem mass spectrometer isotope internal standard method.

The invention belongs to the technical field of new energy batteries, and relates to a lithium ion battery. The lithium ion battery comprises a positive plate, a negative plate, a diaphragm and a non-aqueous electrolyte, wherein the negative plate comprises a negative current collector and a negative material layer arranged on the negative current collector; the negative electrode current collector is a copper foil or a composite copper foil, and the negative electrode material layer comprises a silicon-containing material; the non-aqueous electrolyte comprises a non-aqueous organic solvent, a lithium salt, a first additive and a second additive; the first additive is 1, 3, 6-hexane trinitrile; the second additive comprises a compound as shown in a structural formula 1; the lithium ion battery satisfies the following conditions: 0.1 < = 10 (d + c) * a / b < = 100, 8 < = a < = 30, 20 < = b < = 800, 0.5 < = c < = 4, and 0.1 < = d < = 4. According to the lithium ion battery provided by the invention, the silicon negative electrode is stable in structure, high in energy density and stable in cycle performance.

This invention discloses a Fe-GC@Fe 0 This invention relates to catalysts, their preparation methods, and applications, belonging to the field of water treatment technology. The preparation method of this invention is simple, requires minimal equipment, and yields Fe-GC@Fe catalysts. 0 The catalyst can drive microorganisms in water to metabolize perfluorinated compounds. Under conditions without external energy input, it can effectively remove perfluorinated compounds such as perfluorooctanoic acid, perfluorooctane sulfonic acid, perfluorononanoic acid, and perfluorohexane sulfonic acid from water. The removal rate and defluorination rate both reach more than 80%. Moreover, it is a solid catalyst, which is easy to separate from water, recycle and reuse, and maintain a high removal effect.

The invention discloses an analysis method for simultaneously detecting organochlorine pesticide and polychlorinated biphenyl, which comprises the following steps of: simultaneously extracting organochlorine pesticide and polychlorinated biphenyl in a water sample by adopting a mixed extraction solvent, dehydrating, concentrating and fixing the volume of extract liquor, separating and measuring by adopting a gas chromatography-mass spectrometry method, and quantifying by adopting an internal standard method. When the mixed extraction solvent is n-hexane / dichloromethane with the volume ratio of 9: 1 and 1% by mass of polyethylene glycol 4000 is added, the recovery rates of water samples with the measured concentrations of 5.00 ng / L, 20.0 ng / L, 40.0 ng / L and 80.0 ng / L are 83.6%-95.4%, 91.2%-105.6%, 93.5%-104.7% and 92.8%-106.9% respectively, the relative standard deviations are 6.1%-9.2%, 3.3%-8.2%, 3.2%-6.3% and 3.4%-7.5% respectively, compared with the prior art, the extraction efficiency is remarkably improved, and the method has the advantages that the method is simple, the cost is low, and the method is suitable for industrial production. The accuracy and precision of the method completely meet the determination and analysis requirements for measuring complex water samples.

The invention provides a flexible switching production method and equipment for low cis-polybutadiene rubber (LCBR), solution polymerized styrene-butadiene rubber (SSBR) and hydroxyl-terminated liquid polybutadiene rubber (HTPB), the flexible switching production equipment comprises an initiator production device and a polymerization unit, and the flexible switching production method comprises the following steps: mixing cyclohexane and n-hexane according to a volume ratio of 6.5: 3.5-7: 3, adding an initiator, and stirring to obtain a mixture; forming a mixed solvent; the method comprises the following steps: adding a monomer, an active agent, an initiator and a mixed solvent into a polymerization kettle 31 of a polymerization unit, and carrying out polymerization reaction to obtain a low-cis-polybutadiene, solution polymerized styrene-butadiene or hydroxyl-terminated liquid polybutadiene rubber solution; a novel protection initiator tert-butyl dimethyl siloxy propyl sodium is designed, and hydroxyl-terminated liquid polybutadiene rubber with a controllable structure is prepared through anionic living polymerization. According to the process, shutdown for kettle cleaning is not needed, the low cis-polybutadiene, the solution polymerized styrene-butadiene and the hydroxyl-terminated liquid polybutadiene rubber can be produced on the same polymerization device in a flexible switching manner, and the overall production efficiency is improved.

A method for preparing monodisperse nanoscale calcium fluoride, comprising the following steps: (S1) dispersing calcium long-chain alkylbenzenesulfonate and an acrylate copolymer in a mixed solution of water, n-hexane, and an alcohol to form a stable emulsion A, wherein monomers of the acrylate copolymer comprise (meth)acrylic acid, a polyether macromonomer, and a C1-4 alkyl (meth)acrylate; (S2) dissolving a fluoride salt in water, adding polyvinyl alcohol, and uniformly mixing these materials to obtain a solution B; and (S3) slowly dropwise adding the solution B to the emulsion A under stirring and ultrasonic conditions, and carrying out standing for aging, centrifugal separation, washing, and drying to obtain monodisperse nanoscale calcium fluoride. By using the calcium long-chain alkylbenzenesulfonate with surface activity as a calcium source in combination with homemade acrylate as a dispersing agent, an emulsion is formed in a specific combined solvent, and by dropwise adding a fluorine salt aqueous solution to the emulsion under an ultrasonic condition, nanoscale calcium fluoride with a uniform and controllable particle size can be prepared under the action of a microemulsion.

The invention provides an aluminum oxide aerogel composite material as well as a preparation method and application thereof, and belongs to the technical field of aluminum oxide aerogel preparation. The preparation method provided by the invention comprises the following steps: (1) preparing aluminum sol by taking coal gangue as an aluminum source; (2) mixing the aluminum sol obtained in the step (1) with aluminum silicate fibers, and performing gelation to obtain composite hydrogel; and (3) mixing the composite hydrogel obtained in the step (2) with ethanol, aging, mixing with a modifier, modifying, and carrying out graded normal-pressure drying to obtain the aluminum oxide aerogel composite material, the modifier in the step (3) is one or more of absolute ethyl alcohol, tetraethoxysilane and normal hexane. The alumina aerogel composite material prepared by the preparation method provided by the invention has the characteristics of low density, low heat conductivity coefficient and high strength, and is suitable for the high-temperature processing field of special materials and the aerospace field.

The invention relates to the technical field of organic pollutant degradation, and discloses a mycobacterium and a method for degrading alkane organic pollutants. The Mycobacterium sp. Is named as SLQ-1, the Mycobacterium sp. Is preserved in the China Center for Type Culture Collection on January 15, 2024, and the preservation number is CCTCC No: M 2024107. The Mycobacterium sp. Is named as SLQ-1, and the Mycobacterium sp. Has been preserved in the China Center for Type Culture Collection on January 15, 2024. The mycobacterium can effectively degrade alkane organic pollutants, especially organic pollutants below C8, SLQ-1 can grow and breed with 3-methylpentane as a carbon source and an energy source, 3-methylpentane is efficiently degraded, and the mycobacterium can adapt to a wide temperature range and a wide pH range (the degradation rate of 3-methylpentane can reach 99% or above when the pH is 6-8 and the temperature is 30-40). In addition, the mycobacterium SLQ-1 can also take 2-methylpentane, n-hexane, n-pentane and 2-methylbutane as a carbon source and an energy source, and can efficiently degrade the 2-methylpentane, the n-hexane, the n-pentane and the 2-methylbutane.

The invention provides a method for detecting vitamin B6 related substances in a multivitamin preparation, and belongs to the field of analytical chemistry. According to the method, a high performance liquid chromatograph is adopted, and chromatographic conditions are as follows: an octadecyl silane bonded silica gel chromatographic column is adopted, a mobile phase is a phosphate buffered solution (containing sodium hexanesulfonate)-acetonitrile, and a mobile phase A and a mobile phase B are performed according to a gradient procedure; the flow velocity is 0.8 to 1.2 mL / min; the column temperature is 28-40 DEG C, the detection wavelength is 320-340nm, and the sample size is 20-50mu L. The detection method has the advantages of high sensitivity and good linear relationship, and is suitable for analysis and content determination of vitamin B6 related substances in various vitamin preparations.

The invention discloses a Fe-GL-Fe < 0 > catalyst and a preparation method and application thereof, and belongs to the technical field of water treatment. The preparation method is simple, the requirement for equipment is low, the prepared Fe-GL-Fe < 0 > catalyst can effectively remove perfluorinated compounds such as perfluorooctanoic acid, perfluorooctane sulfonic acid, perfluorononanoic acid and perfluorooctane sulfonic acid in water under the environment atmosphere condition without external energy input, and the removal rate and the defluorination rate are both larger than 95%; the catalyst belongs to a solid catalyst, is convenient to separate from water, is recycled, keeps a high removal effect, and is low in metal ion dissolution rate.

The invention relates to the technical field of chemical detection, in particular to a sample pretreatment method and a GC-MS (Gas Chromatography-Mass Spectrometer) method for simultaneously detecting glycidol and monochloropropanol in heated cigarette aerosol. The sample pretreatment method for simultaneously detecting the glycidol and the monochloropropanol in the heated cigarette aerosol comprises the following steps: capturing particulate matters in the heated cigarette aerosol; mixing the trapping material with ethyl acetate and an internal standard substance, extracting to obtain an extracting solution, and diluting with n-hexane; adding heptafluorobutyrylimidazole to perform derivatization reaction, washing with water after the derivatization reaction is completed, and drying to obtain a solution to be detected. According to the present invention, ethyl acetate is adopted for extraction, and detection analysis can be performed through dilution, HFBI derivatization, water washing and drying, such that the sample pretreatment step is substantially simplified, and the analysis sensitivity and the accuracy of the simultaneous detection of the three compounds such as the glycidyl, the 3-chloro-1, 2-propylene glycol and the 2-chloro-1, 2-propylene glycol can be easily improved.

A method for preparing a composite nanofiltration membrane based on aspartic acid modified carbon quantum dots belongs to the field of nanofiltration membrane preparation, and comprises the following steps: 1) dissolving citric acid monohydrate in water, adding aspartic acid, heating and stirring, and then adding a sodium hydroxide solution to adjust pH; (2) carrying out suction filtration on the mixed solution obtained in the step (1) by using a microfiltration membrane, dialyzing and purifying in ultrapure water, and freeze-drying to obtain the aspartic acid modified carbon quantum dots; (3) fixing a polysulfone base membrane in a mold, preparing a water-phase solution containing anhydrous piperazine and aspartic acid modified carbon quantum dots, pouring the water-phase solution into the mold to be in contact with the base membrane, and air-drying; and 4) preparing a trimesoyl chloride solution by using n-hexane as a solvent, pouring the trimesoyl chloride solution into a mold for contact, and finally drying to obtain the composite nanofiltration membrane.When the concentration of the aspartic acid modified carbon quantum dots is 2000ppm, the water flux reaches 168LMH, the retention rate reaches a peak value when the concentration of the quantum dots is 1000ppm and is 1.3 times of that of a base membrane, and the composite nanofiltration membrane shows excellent performance.

The invention relates to a melamine sponge with a chitosan-wheat straw biochar coating as well as a preparation method and application of the melamine sponge. The preparation method comprises the following steps: crushing wheat straws, and pyrolyzing under an anaerobic condition to obtain biochar; the biochar is soaked in a Prussian blue dispersion liquid for modification, and Prussian blue modified biochar is obtained; dispersing the material in a chitosan acetic acid solution for reaction to form a chitosan-charcoal composite system; adding PDMS (Polydimethylsiloxane) to carry out siloxane reaction to form stable composite sol; and finally, spraying the composite sol on the surface of the pretreated melamine sponge to form the super-hydrophobic coating. Through the synergistic effect of Prussian blue, chitosan and PDMS, the hydrophobicity and oil adsorption capacity of the material are remarkably improved, the water contact angle of the obtained sponge material can reach 168 degrees, the adsorption capacities to normal hexane and chloroform respectively reach 34 g / g and 80 g / g, and the sponge material has good cycle stability and wide application prospects in the fields of oil-water separation and environmental pollution treatment.

The invention provides a preparation method of alpha, omega-diiodo perfluoroalkane, and belongs to the technical field of iodo perfluoroalkane synthesis. The preparation method disclosed by the invention comprises the following steps: under a protective atmosphere, enabling a nano flower type magnesium fluoride catalyst, 1, 2-diiodo tetrafluoroethane and tetrafluoroethylene to react, so as to obtain 1, 4-diiodo perfluorobutane and 1, 6-diiodo perfluorohexane. The nano flower type magnesium fluoride catalyst has high specific surface area and abundant coordination unsaturated sites, can effectively activate reactant molecule bonding sites, and avoids the problems of side reaction and catalyst deactivation caused by free radical paths; by optimizing the pore structure and reaction conditions of the catalyst, efficient synergistic conversion of IPF-2 and TFE can be realized, and the selectivity and yield of IPF-4 and IPF-6 are remarkably improved. The method provided by the invention has the advantages of mild conditions, safe operation, adjustable product distribution and the like, and meets the requirements of industrial production on high-selectivity fluorine-containing bifunctional compounds.

This invention discloses a butyrolactone compound with multidrug resistance reverse transcription activity, its preparation method, and its uses. The compound's structural formula is shown in Figure I. The preparation method includes the following steps: fermenting *Aspergillus pyrolyticus* (accession number CCTCC NO: M2014086) to obtain a butyrolactone fermentation product; extracting the fermentation product with ethyl acetate to obtain a crude extract; degreasing the crude extract with hexane and dichloromethane to obtain a final extract; and purifying the final extract using normal-phase silica gel column chromatography, reversed-phase medium-pressure column chromatography, and reversed-phase semi-preparative high-performance liquid chromatography. The advantage of this butyrolactone compound is that it possesses multidrug resistance reverse transcription activity and the ability to regulate P-gp-mediated drug efflux in multidrug-resistant cell lines, making it a potential drug for treating multidrug-resistant cancers.

The invention discloses an air environment preparation method of a perovskite blue light emitting diode. The air environment preparation method comprises the following steps: S1, preparing a hole injection layer on the surface of an ITO anode; s2, preparing an interface modification layer on the upper surface of the hole injection layer to obtain an intermediate substance; s3, preparing a perovskite blue light emitting layer on the interface modification layer to obtain a substrate with a light emitting layer; s4, evaporating an electron injection layer on the surface of the light-emitting layer; and S5, evaporating a cathode on the surface of the electron injection layer. An alkane anti-solvent (isooctane, n-octane and n-hexane) is introduced for treatment in the process of processing a light-emitting layer by a solution, so that the brightness and the electroluminescent external quantum efficiency of the device are improved, and compared with the traditional process of preparing blue light PELEDs in an air environment by adopting diethyl ether as a treatment solvent, the electroluminescent external quantum efficiency of the device is improved by about one time. The electroluminescent spectrum of the perovskite blue light PeLEDs disclosed by the invention can show relatively good stability under the driving of different voltages and time.

The invention discloses a water treatment filtering material and a preparation method thereof, and relates to the technical field of water treatment. When the water treatment filtering material is prepared, alkaline lignin, epichlorohydrin and triethylenetetramine are subjected to a reaction through a reverse suspension cross-linking technology, and lignin porous microspheres are prepared; carrying out reaction on the lignin porous microspheres and picolinamide ligands to obtain modified lignin porous microspheres; 3-mercaptopropyltriethoxysilane and titanium dioxide are subjected to a reaction, and modified titanium dioxide is prepared; the preparation method comprises the following steps: reacting pyromellitic dianhydride, 1, 4-diaminobutylene and 4 ', 4-diaminodiphenyl ether to prepare functionalized polyamide; the functional polyamide, the modified lignin porous microspheres and the modified titanium dioxide are prepared into a spinning solution, and a polyamide membrane is prepared through electrostatic spinning; and carrying out liquid reaction on bromohexane on the polyamide membrane to obtain the water treatment filtering material. The prepared water treatment filtering material has excellent antibacterial property, heavy metal adsorption property, dye removal property and mechanical property.