146 results about "Nitrophenol" patented technology

The invention belongs to the field of soil environment pollution simulation and prediction, and provides a prediction method based on a two-point chemical unbalanced model, which is used for quantitatively evaluating the effect of regulating and controlling the migration behavior of p-nitrophenol in acid red soil by straw stalk biochar. According to the method, a biochar-red soil composite medium system is constructed, a soil column leaching experiment is carried out to obtain penetration curve data, a two-point chemical unbalance model in CXTFIT software is utilized to carry out parameter inversion, and key parameters such as a retardation factor, a two-region distribution coefficient, a mass transfer coefficient and a liquid phase degradation coefficient are accurately identified. Model verification shows that the goodness of fit is high, and a parameter change rule reveals the inherent mechanism of enhancing the pollutant retention capacity, changing the proportion of fast and slow adsorption sites and influencing mass transfer kinetics by the biochar. Based on the verified model, the long-term migration behavior and pollution risk of p-nitrophenol under different environmental conditions can be simulated, and a scientific basis is provided for groundwater pollution control and remediation strategy optimization.

This invention relates to a method for preparing and applying polyamides from a monomer containing 7-methyldibenzo[c,g]carbazole and triphenylamine: 4-({9-[(4-aminophenyl)(4-methoxyphenyl)amino]-7-methyldibenzo[c,g]carbazole-5-yl}(4-methoxyphenyl)amino)aniline. To address the problems of low solubility, difficulty in film formation, poor cycling stability, narrow color change range, and limited functionality in polyamide materials, this invention constructs two triphenylamine groups on 7-methyldibenzo[c,g]carbazole and introduces a methoxy group onto the triphenylamine to increase the polymer's solubility and stability. The polymer of this invention exhibits excellent electrochromic properties, including excellent cycling stability, fast switching time, and high optical contrast. Furthermore, to address the material's multifunctionality, a naphthalene unit is added to the molecular structure, resulting in a polymer with fluorescent emission. This invention can be applied to displays, rearview mirrors, camouflage applications, and the fluorescence detection of p-trinitrophenol.

The invention discloses a synthesis method of 5-nitro-2-aminophenol, which comprises the following steps: by using 2-chloro-4-nitroaniline as a raw material, providing an amino protecting group by using di-tert-butyl dicarbonate ester to obtain a compound 3; carrying out hydrolysis reaction in an alkaline environment to hydrolyze chlorine groups on benzene rings into hydroxyl groups to obtain a compound 4; and removing an amino protecting group under an acidic condition to obtain the 5-nitro-2-aminophenol. According to the method, 2-chloro-4-nitroaniline is used as a starting raw material, compared with expensive ortho-aminophenol, the cost of the raw material can be remarkably reduced, use of expensive catalysts in the hydrolysis process is avoided through amino protection, generation of the byproduct 2-amino-4-nitrophenol is effectively reduced, and the yield of the 2-chloro-4-nitrophenol is increased. And the synthesized 5-nitro-2-aminophenol has relatively high purity (99.5%) and relatively high yield (-86%). The method has the advantages of conventional production steps and conventional process equipment, and has a good application prospect.

The invention discloses an application of a copper nano-cluster with stable ascorbic acid in detection of p-nitrophenol, the copper nano-cluster with stable ascorbic acid is used as a fluorescent probe, and the detection of p-nitrophenol is realized through a fluorescent sensing method. Due to the quenching effect of p-NP, the fluorescence intensity of the system is obviously reduced in the presence of p-NP. The p-NP concentration can be quantitatively detected by comparing the fluorescence intensity of the copper nano-cluster and the fluorescence intensity of a quenching system. The method is simple, sensitive and high in selectivity, does not need complex fluorescent dye labeling, shows remarkable potential for p-NP detection, and has a good application prospect in the aspects of food, medicine and the like.

This invention provides compounds and methods of application that possess both broad-spectrum antifungal activity and plant-induced resistance, belonging to the field of agricultural technology. It addresses the problem that "traditional pure immune inducers must be applied before disease onset, making it difficult to meet the full-cycle control needs of disease prevention and treatment in the field." Compared to the previously developed PC1 and PC20, the two compounds of this invention, 2,4-dibromo-6-nitrophenol and 7-deazon-2'-deoxy-7-iodoadenosine, can both inhibit the growth of rice blast fungus and significantly improve rice resistance to rice blast through foliar spraying, meeting the full-cycle control needs of disease prevention and treatment in the field. Furthermore, these two compounds can directly inhibit the growth of various fungal pathogens such as peanut white mold, tomato gray mold, wheat scab, rice bakanae disease, rice false smut, mango malformation, and banana wilt.

This invention provides a method for screening β-galactosidase inhibitors, belonging to the field of pharmaceutical technology. The first step of this method uses fluorescence sensing technology to rapidly identify natural products with β-Gal inhibitory activity. The principle is based on the fluorescence quenching property of p-nitrophenol (PNP) on sulfur quantum dots (SQDs); β-Gal catalyzes the hydrolysis of p-nitrophenyl-β-D-galactopyranoside (PNPG) to generate the specific product PNP; in the presence of β-Gal, PNPG can be enzymatically catalyzed to generate PNP, quenching the fluorescence of SQDs; when screened for β-Gal inhibitory activity, the fluorescence of SQDs can be restored. The second step uses affinity chromatography to capture components in samples with β-Gal inhibitory activity. This method involves immobilizing β-Gal on a support material, eluting with a solvent to obtain components that can bind to β-Gal, and then using liquid chromatography-mass spectrometry (LC-MS) to identify the components. This method can rapidly and accurately screen β-Gal inhibitors from natural products.

The invention discloses an aluminum alloy material easy to oxidize and color and a preparation method thereof.The aluminum alloy material is prepared from, by weight, 20-25 parts of aluminum alloy powder, 5-10 parts of graphene, 4-6 parts of p-nitrophenol, 0.5-1 part of concentrated bromine water and 4-7 parts of magnesium powder. And graphene treatment, aluminum alloy and graphene dispersion treatment, drying, water washing and vacuum hot pressing are carried out. Graphene is doped with the aluminum alloy, the comprehensive performance of the aluminum alloy can be remarkably improved, the hardness can be improved, the electrical conductivity and the thermal conductivity can be remarkably improved, halogen elements are introduced, the activity of the aluminum alloy is improved, the oxidized capacity is improved, the coloring efficiency is improved, and the flame retardant property is improved; and the magnesium powder is added, so that the stability of the system is protected, and the hardness of the system is improved.

The invention discloses a water-based photoresponse type rosin-based aggregation-induced emission amphiphilic molecule as well as a preparation method and application thereof. The molecular structural formula of the water-based light response type rosin-based AIE amphiphilic molecule is shown in the specification, or n ranges from 15 to 30. According to the water-based light-responsive rosin-based AIE amphiphilic molecule, a tetraphenyl ethylene or cyanostilbene fluorophore is introduced into the anhydride part of maleopimaric acid through an imidization reaction, and groups such as sodium carboxylate, amino acid sodium or polyethylene glycol are introduced into the carboxylic acid position to prepare the water-based light-responsive rosin-based AIE amphiphilic molecule. The solid of the molecule has blue fluorescence emission, and can be used for dyes or solid anti-counterfeiting materials. A photoresponsive AIE aqueous solution is prepared by using the amphiphilic molecule alone or compounding the amphiphilic molecule with dodecyl polyoxyethylene ether, and the photoresponsive AIE aqueous solution can be used for water-based anti-counterfeiting ink, cell imaging or 4-nitrophenol detection and the like.

The application discloses a copper oxide nanowire loaded silver monatomic catalyst, a preparation method and application thereof, and comprises a substrate, CuO nanowires and metal Ag monatomic atoms loaded on a CuO nanowire electrode layer; the substrate is a commercial copper foam, and the substrate is used for providing a copper source and preparing an array material of the metal Ag monatomic atoms on the CuO nanowires. The application adopts the above-mentioned copper oxide nanowire loaded silver monatomic catalyst, the preparation method and the application thereof, through silver monatomic atom modification, copper-silver metal interaction jointly regulates an intermediate product in an adsorption electrocatalytic reduction process, excellent electrocatalytic nitrophenol reduction performance is obtained, and the application is suitable for environmental pollution treatment and pharmaceutical synthesis development fields.

The invention discloses a colorimetric detection method for cMyBP-C protein based on nano-enzyme activity, preparation of a bismuth selenide / nano-gold composite material and application of the bismuth selenide / nano-gold composite material in protein detection. The method comprises the following steps: performing ultrasonic stripping on a bismuth selenide block to obtain a few-layer bismuth selenide dispersion liquid; and then sequentially adding a sodium borohydride aqueous solution and a chloroauric acid aqueous solution under a stirring condition, and carrying out in-situ reduction to form gold nanoparticles loaded on the surface of bismuth selenide. The composite material has the capability of catalyzing reduction of p-nitrophenol into p-aminophenol, and the color of the solution is changed from yellow to colorless. After the cMyBP-C antibody is modified on the surface of the composite material, the catalytic activity is inhibited; after a to-be-detected sample is added, the antibody and the protein are specifically combined to cause dissociation, and the catalytic activity is recovered. The cMyBP-C protein is quantitatively detected by observing the color change of the solution or monitoring the reduction of the ultraviolet absorbance at 400 nm.

The invention relates to the technical field of gas impurity removal, and discloses a metal modified molecular sieve as well as a preparation method and application thereof. The method comprises the following steps: (1) mixing a metal salt, a nitrogen-containing micromolecule complexing agent, a nitrogen-containing micromolecule dispersing aid and ethanol to obtain a mixed solution, and then adding a molecular sieve for mixing to obtain a mixture; (2) drying the mixture obtained in the step (1), and then roasting; wherein the metal in the metal salt is selected from at least one of Mg, Ca, Sr and Ba; the nitrogen-containing micromolecule complexing agent is selected from at least one of 2-nitrophenol, 3-nitrophenol and 4-nitrophenol. The metal modified molecular sieve prepared by the method has very high adsorption activity on nitrous oxide, oxygen-enriched liquid air containing nitrous oxide is treated, the content of nitrous oxide can be reduced to 5 ppm or below, and the whole process is low in energy consumption, does not generate new impurities, and is green and environment-friendly.

The application provides a polypeptide vaccine delivery carrier, which is a phenylalanine-based polyester amide polymer prepared from triethylamine, p-nitrophenol, L-phenylalanine and butanediol. + The polypeptide vaccine has good stability, high antigen presentation effect, and can induce the body to produce effective antitumor CD8 T cell immune response, inhibit tumor growth and metastasis, and improve the effect of immunotherapy.

The present application relates to the technical field of organic synthesis, and particularly relates to a zinc-based fluorescent probe containing a pyridyl carboxylic acid type component, and a preparation method and application thereof. 22 H 14 N3O2)(CHO2)(H2O)·C3H7NO·3H2O; the zinc-based fluorescent probe containing the pyridyl carboxylic acid type component belongs to a monoclinic system, and a space group is P 2 1 / c ; cell parameters are a = 7.2925(2) Å, b = 26.6839(8) Å, c = 12.8618(4) Å, α = 90°, β = 105.5770(10)°, gamma = 90°. The zinc-based fluorescent probe has good thermal stability and large light emission intensity, the preparation method is simple, and the zinc-based fluorescent probe can be used as a fluorescent sensor to detect Fe 3+ and 2,4,6-trinitrophenol in a DMF solution with high sensitivity and high selectivity.

The application discloses a fluorescence analysis system for specific response to p-nitrophenol based on gold nanoclusters AuNCs@CFP, 200 muL of gold nanoclusters AuNCs@CFP, 500 muL of PB buffer solution with pH=10 and to-be-detected p-nitrophenol are diluted to 4 mL, the fluorescence intensity of the mixture is determined at an excitation wavelength of 334 nm after reaction at 45 DEG C for 50 min, the concentration of the to-be-detected p-nitrophenol is calculated according to the determined fluorescence intensity and a regression equation, the linear concentration range of the p-nitrophenol is 1.25-40 muM, the regression equation is F0 / F i =0.0258C+1.0003, F0 and F i are the fluorescence intensities of the mixture before and after the addition of the p-nitrophenol respectively, the correlation coefficient R 2 =0.9922, the detection limit LOD is 1.92 muM, the concentration of the p-nitrophenol is 25 muM, the relative standard deviation RSD is 1.13% in 11 repeated determinations. The preparation method of the gold nanoclusters AuNCs@CFP in the application is simple and easy to synthesize, and the fluorescence performance of the gold nanoclusters AuNCs@CFP is excellent.

The invention discloses a water-soluble fertilizer for promoting swelling and coloring of crop fruits. The water-soluble fertilizer is prepared from the following raw materials: 30 to 50 parts of herba portulacae fermentation liquor, 15 to 25 parts of potassium nitrate, 10 to 20 parts of monopotassium phosphate, 2 to 8 parts of chelated trace elements, 2 to 4 parts of polyglutamic acid, 1 to 3 parts of compound sodium nitrophenolate and 1 to 3 parts of betaine. The invention belongs to the technical field of agricultural fertilizers, and particularly provides a water-soluble fertilizer for promoting fruit swelling and coloring of crops, which is characterized in that inert precursor substances in purslane are converted into efficient active components by a fermentation technology, and alpha-linolenic acid derivatives generated by fermentation of the purslane stimulate expression of relaxation proteins in fruit cell walls to achieve a fruit swelling effect.

The invention discloses a texturing process of a single crystal battery piece. The texturing process comprises the following steps: S1, performing pre-texturing treatment on a silicon wafer by adopting pre-texturing liquid; s2, texturing the silicon wafer by adopting texturing liquid; the prefabricated down liquid comprises polyvinylpyrrolidone and polyvinyl alcohol; the texturing liquid comprises inorganic alkali, a defoaming agent and a catalyst; the inorganic base is selected from at least one of sodium hydroxide and potassium hydroxide, and the defoaming agent is selected from at least one of dodecyl trimethyl ammonium chloride, hexadecyl trimethyl ammonium chloride, octadecyl trimethyl ammonium chloride, diethylene glycol, triethylene glycol and tetraethylene glycol. The catalyst is selected from at least one of sodium 5-nitro-o-methoxyphenolate, sodium o-nitrophenolate and sodium p-nitrophenolate. A nucleating agent solution is adopted to carry out texturing pretreatment on a silicon wafer, then alkali treatment texturing is carried out on the silicon wafer, and the liquid changing period of the texturing process is long; and the cell pieces prepared by taking the polyvinylpyrrolidone and the polyvinyl alcohol as the combined nucleating agent are relatively small in inter-piece color difference.

The present application belongs to the technical field of biomass hard carbon, and particularly relates to a preparation method and application of a high-rate hard carbon negative electrode material. The preparation steps are as follows: biomass raw materials are pre-carbonized under a protective atmosphere to obtain a pre-carbonized product; the pre-carbonized product is added into a p-nitrophenol solution, stirred uniformly, poured into a reaction kettle containing a polytetrafluoroethylene carbonization bottle, and subjected to a hydrothermal reaction in a blast drying oven to obtain pretreated material, which is then crushed to obtain crushed material; the crushed material is subjected to high-temperature heat treatment under an inert atmosphere to obtain heat-treated material; the heat-treated material is mixed with liquid pitch, fused in a high-speed fusion machine to obtain fused material; and the fused material is subjected to surface modification under an inert atmosphere to obtain a high-rate hard carbon negative electrode material after cooling. The finished material can be applied in sodium ion batteries. The present application introduces nitrogen atoms, optimizes defects, improves the sodium ion transmission rate, and improves the rate performance.

The invention discloses a method for synthesizing mesalazine and application of mesalazine. The method comprises the following steps: introducing p-nitrophenol, formic acid and a Cu-Co-coated MFI-NS molecular sieve catalyst into a continuous flow reaction zone, and sequentially carrying out electrophilic substitution and nitro hydrogenation cascade reaction at normal pressure and 50-70 DEG C; the catalyst has a micropore-mesopore stepped pore channel, and contains a Cu0 metal cluster and a framework Co < 2 + > acid site. And separating, acidifying and crystallizing the reaction liquid to obtain a finished product. According to the invention, the shape-selective selectivity and difunctional synergistic effect of the molecular sieve are utilized, high conversion rate (gt, 98%) and high selectivity (gt, 94%) under mild conditions are realized, the product purity is greater than or equal to 99.5%, and the Cu / Co residue meets the ICHQ3D standard. The catalyst can be recycled for 10 times or more, the yield is reduced by 5% or less, iron mud pollution of a traditional iron powder method and the metal leaching risk of a noble metal catalyst are thoroughly eliminated, and the method has the remarkable advantages of being environmentally friendly, efficient, low in cost, easy to industrially amplify and the like and is suitable for preparing the medicine for treating the inflammatory bowel disease.

The application discloses a synthesis method of 3,4-dimethyl-6-nitrophenol, which comprises the following steps: S1, 3,4-dimethylphenol and silica gel are added into an organic solvent, after the 3,4-dimethylphenol is dissolved, heating and concentration are carried out at 50-80 DEG C, until the organic solvent is evaporated, and the silica gel containing 3,4-dimethylphenol is obtained; S2, cerium ammonium nitrate and silica gel are added into an organic solvent, after the cerium ammonium nitrate is dissolved, heating and concentration are carried out at 50-80 DEG C, until the organic solvent is evaporated, and the silica gel containing cerium ammonium nitrate is obtained; S3, a silica gel column is taken, the silica gel containing 3,4-dimethylphenol and the silica gel containing cerium ammonium nitrate are added into the silica gel column, and then mixed solvents are used for column pressing; yellow oil is obtained after concentration; S4, the yellow oil is passed through a silica gel column, elution is carried out by using an eluent, and after concentration, the product 3,4-dimethyl-6-nitrophenol is obtained. The synthesis method of 3,4-dimethyl-6-nitrophenol improves the reaction yield, reduces the cost, and is green and environment-friendly.

This invention provides a method for preparing carbon quantum dots, their application in the detection of 4-nitrophenol and curcumin, a concentration detection method, and a visualization detection method. The method involves mixing tris(hydroxymethyl)aminomethane and phloroglucinol in a solvent, followed by heating in a reaction vessel to obtain the carbon quantum dots. This invention provides a simple and low-cost method for preparing carbon quantum dots, enabling rapid and low-cost detection of 4-NP and curcumin, thus meeting the detection needs for both.

The invention discloses a silver-palladium alloy nanowire and a preparation method and application thereof, and belongs to the technical field of nano alloy materials. The preparation method comprises the following steps: (1) adding an aqueous solution of hexadecyl trimethyl ammonium bromide and an aqueous solution of dopamine hydrochloride into an aqueous solution of silver nanowires, uniformly stirring, dropwise adding an aqueous solution of sodium chloropalladate, and continuously stirring until the reaction is completed to obtain a reaction product; and (2) carrying out centrifugal washing on the reaction product to obtain the silver-palladium alloy nanowire. The prepared silver-palladium alloy nanowire material is used for catalytic reduction of 4-nitrophenol, verification of a photothermal effect and glutathione level detection, so that the application of the silver-palladium alloy nanowire material in the field of catalysis is effectively expanded; and a brand new nano-alloy material and an application approach are provided for high-sensitivity and high-selectivity detection of glutathione level due to the exertion of a photothermal effect.

The invention discloses an N and P co-doped charcoal-silicon dioxide composite material and application thereof in adsorbing phenols in oilfield wastewater, and belongs to the technical field of environmental functional materials. The composite material comprises a biochar matrix, silicon dioxide, and an N element and a P element which are co-doped on the surface of the material and in a skeleton. Silicon dioxide serves as a framework, the high-porosity structure of the material is supported and maintained, the thermal stability of the material is improved, rich surface active sites are introduced through co-doping of N and P, and the adsorption capacity of the material to phenolic pollutants is remarkably improved through the synergistic effect of the silicon dioxide and the N and P. The adsorption capacity of the material to typical oilfield phenols such as phenol, cresol, chlorophenol, nitrophenol and the like is 150-200 mg / g, the adsorption efficiency can reach 96% or above, and the recycling performance can be good through acid and alkali heat treatment. The invention effectively solves the problems of poor adsorption effect, high material cost, insufficient stability, secondary pollution and the like in oilfield wastewater phenol treatment.

The application discloses a preparation method of nitrophenol, which comprises the following steps: taking a nitrous acid compound as a nitro source, and reacting the nitrous acid compound with a phenol compound in a solvent under the catalysis of an acyl chloride or an anhydride catalyst to generate the nitrophenol. The application has the advantages of wide application range of substrates, mild reaction condition, short reaction time, simple operation, no use of strong acid and metal catalyst, environmental friendliness, excellent yield, and the like, and the yield can reach 95%.

The application discloses a method for analyzing nitrobenzene and nitrophenol compounds in waste acid samples, which comprises the following steps: mixing the waste acid sample with a certain amount of pure water, adding a substitute, carrying out liquid-liquid extraction with dichloromethane, repeatedly extracting twice to obtain bottom organic phase extract A, and water phase sample B is reserved for use; adding the extract A into pure water to wash the acid, obtaining organic phase A and water phase C, combining water phases B and C, adjusting the pH to neutral, carrying out liquid-liquid extraction twice with dichloromethane to obtain organic phase D; combining organic phases A and D, and carrying out dehydration and purification treatment on the organic phase sample; carrying out concentration treatment on the sample extract to obtain a to-be-tested sample solution containing nitrobenzene and nitrophenol compounds; adding an internal standard to the to-be-tested sample solution to detect the content of nitrobenzene and nitrophenol compounds. The method solves the problems that the waste acid sample is highly acidic and corrosive and is not friendly to instruments, and can simultaneously detect nitrobenzene and nitrophenol compounds in the waste acid sample, so that it is not necessary to separately detect and separately put on machines due to different acidities of extraction environments of nitrobenzene and nitrophenol compounds, and the detection rate of the sample is greatly improved.

The invention relates to the technical field of photocatalysts, in particular to a nonmetal plasmon heterojunction material, a preparation method and application thereof and a method for preparing p-aminophenol through reduction of p-nitrophenol. The nonmetal plasmon heterojunction material provided by the invention comprises a C3N4 nanosheet and a WO3-x nanoplate (x is 0.1 to 0.3) positioned on the surface of the C3N4 nanosheet. The WO3-x local surface plasmon characteristic can effectively expand the spectral response range of the non-metal plasmon heterojunction material in a visible region to a near-infrared region, and the light absorption efficiency of the non-metal plasmon heterojunction material is remarkably enhanced. The nonmetal plasmon heterojunction material provided by the invention can realize efficient reduction of p-nitrophenol based on the synergistic effect of an interface heterojunction, a built-in electric field and oxygen vacancies, is high in selectivity, has excellent photocatalytic activity for reduction of p-nitrophenol, and is excellent in photocatalytic activity stability.

The application discloses a method for synthesizing benoxacor, and belongs to the technical field of chemical organic synthesis. The method comprises the following steps: taking DMF as a solvent, fully reacting ortho-nitrophenol with monochloroacetone and alkali at a certain temperature, centrifuging after the reaction is completed, obtaining a first filter cake and a DMF solution of 2-nitro-2-phenoxypropanone, removing part of the DMF through vacuum distillation, detecting the content of chloroacetone in the gas chromatograph, and adjusting the mass concentration of the 2-nitro-2-phenoxypropanone DMF solution to 10-20% after the content of chloroacetone is detected to be lower than 0.02% by using the area normalization method; then, adding Raney nickel into the 2-nitro-2-phenoxypropanone DMF solution, and performing hydrogenation reaction by passing hydrogen; after the reaction is completed, the upper clear liquid is extracted, and 3,4-dihydro-3-methyl-2H-1,4-benzoxazine DMF solution is obtained through filtration; then, an acid-binding agent alkali is added, and acylation reaction is performed by dropwise adding dichloroacetyl chloride, so as to synthesize benoxacor. The method can greatly simplify the operation process of frequently changing solvents in the process of synthesizing benoxacor, and can avoid the generation of a large amount of waste brine.

The invention discloses a resin material for 3D printing and a preparation method thereof, and relates to the technical field of photosensitive resin materials. When the resin material for 3D printing is prepared, 3-isocyanate propyl methyl dimethoxy silane is blocked by p-nitrophenol, so that blocked 3-isocyanate propyl methyl dimethoxy silane is prepared; the preparation method comprises the following steps: carrying out condensation on blocked 3-isocyanate group propyl methyl dimethoxy silane, 3-mercaptopropyl methyl dimethoxy silane and hexamethyldisiloxane, so as to prepare blocked isocyanate group mercapto silicone oil; the preparation method comprises the following steps: loading a resorcinol bis (diphenyl phosphate) flame retardant on glass flakes modified by silane to prepare flame-retardant modified glass flakes; the preparation method comprises the following steps: reacting epoxy acrylate, blocked isocyanate sulfydryl silicone oil, acryloyl morpholine and a photoinitiator to prepare photosensitive resin, and compounding the photosensitive resin with flame-retardant modified glass flakes to prepare the resin material for 3D printing. The prepared resin has high mechanical property, flame retardant property and thermal stability.

This application relates to the field of materials technology, providing a chitosan-polyacrylonitrile composite material, its preparation method, and its application. The general structural formula of the chitosan-polyacrylonitrile composite material is as follows: This application uses inexpensive chitosan and polyacrylonitrile fiber as raw materials to develop a novel chitosan-polyacrylonitrile composite material, overcoming the solubility limitation of chitosan under acidic conditions and simultaneously enhancing its adsorption capacity for phenolic compounds and heavy metals. It exhibits higher selectivity for target pollutants, especially among eight different phenolic compounds (phenol, 4-methylphenol, 4-chlorophenol, 4-nitrophenol, hydroquinone, catechol, resorcinol, and phloroglucinol), showing excellent adsorption performance for hydroquinone, with an adsorption capacity as high as 316.84 mg·g⁻¹. ‑1 Furthermore, this application addresses the soft metal ion Hg. 2+ Its adsorption capacity is outstanding, with a maximum adsorption capacity of 237.18 mg·g⁻¹. ‑1 .

This invention provides a method for preparing chiral N-tert-butylsulfonamide compounds. The method uses N-tert-butylsulfonylimide as a starting material, employs Mn(CO)₅Br and a chiral PNN ligand as catalysts, and an alcohol as a solvent. A hydrogenation reaction occurs in this homogeneous catalytic system, yielding axially chiral diaryl nitrophenol compounds in high yield (99%) and with high ee values ​​(>99%). This reaction has the advantages of high efficiency, mild conditions, and environmental friendliness. The obtained chiral N-tert-butylsulfonamide can be deprotected with a sulfonyl protecting group to obtain the corresponding chiral primary amine.

The application discloses a high-temperature-resistant high-activity lipase mutant and application thereof, wherein the mutant is obtained by substituting at least one amino acid in three positions of 25th, 242nd and 283rd of the amino acid sequence shown in SEQ ID No. 1; the threonine in the 25th position is mutated into methionine, the serine in the 242nd position is mutated into glycine or alanine, and the aspartic acid in the 283rd position is mutated into proline. The application obtains the mutant by mutating the wild-type lipase, and the mutant can efficiently catalyze the generation of p-nitrophenol from p-nitrophenol palmitate, and the mutant shows significantly enhanced resistance under high-temperature conditions, thereby improving the high-temperature catalytic efficiency and effectively expanding the application range of the lipase under high-temperature conditions.