1759 results about "Ketone" patented technology

Glucose and ketones may be dysregulated singularly or concurrently in certain physiological conditions and may be advantageously assayed together using an analyte sensor capable of detecting both analytes. Certain analyte sensors capable of dual detection may comprise a first working electrode and a second working electrode, a ketones-responsive active area disposed upon a surface of the first working electrode, a glucose-responsive active area comprising a glucose-responsive enzyme disposed upon a surface of the second working electrode, a membrane having a first portion overcoating the ketones-responsive active area and a second portion overcoating the glucose-responsive active area, in which the first portion and the second portion have different compositions. The ketones-responsive active area comprises an enzyme system comprising at least two enzymes that are capable of acting in concert to facilitate detection of ketones.

The invention discloses a rare-earth metal arylamine group compound as well as preparation method and application thereof. The invention discloses the rare-earth metal arylamine group compound which is characterized in that a general formula of the rare-earth metal arylamine group compound is (2,6-R12PhNH)5LnLi2(THF)2, wherein Ln is a rear-earth metal selected from one of neodymium, samarium, ytterbium or yttrium; R1 is selected from one of hydrogen, methyl or isopropyl. The rare-earth metal arylamine group compound has the advantages that the rare-earth metal arylamine group compound has a definite structure; raw materials used in the preparation method are simple, easily obtained and cheap; the reaction process is simple and easily operated; the rare-earth metal arylamine group compound product is conveniently purified and the yield of the product is high; the rare-earth metal arylamine group compound has a high activity when acting as a single component catalyst to catalyze a hydrogen phosphine reaction of aldehyde or ketone and phosphite ester; the use amount of the catalyst is less; the yield is high; a substrate has wide universality; a new and simple method is provided for synthesis of a-hydroxyphosphonate.

The invention belongs to the technical field of hair care products, and particularly relates to composite acid gel for scalp care and a preparation method thereof. Salicylic acid, glycolic acid, piroctone azelate olamine salt, echinacea purpurea-lactic acid bacteria yeast, an emulsifier and water are combined, wherein the echinacea purpurea-lactic acid bacteria yeast is prepared by performing enzymolysis on echinacea purpurea through bacillus subtilis protease and then performing aerobic fermentation with lactic acid bacteria. Salicylic acid, glycolic acid and azelaic acid in the composite acid gel are compounded, so that stimulation of salicylic acid is weakened, and the effect of dissolving hair follicle grease is reserved; glycolic acid and azelaic acid are added to accelerate keratin metabolism, regulate sebum secretion and create safe and healthy shielding for the scalp environment, and polysaccharide and flavonoid compounds in the echinacea purpurea-lactic acid bacteria leavening are beneficial to exerting the anti-oxidation and immune regulation effects of the echinacea purpurea-lactic acid bacteria leavening. Therefore, the composite acid gel provided by the invention is green, safe and non-irritant, the preparation method is simple and convenient, and the composite acid gel can be used for inhibiting bacteria and reducing scalp inflammation.

The invention discloses a polyetherketoneketone high-temperature-resistant wear-resistant non-stick coating and a preparation method thereof. The coating is prepared from the following components in parts by mass: 13 to 30 parts of a resin matrix group (containing 12 to 25 parts of titanium modified polyether ketone ketone resin, 1 to 5 parts of fluorine-free viscous resin and 0.65 to 6 parts of aluminum oxide), 0.5 to 3 parts of a nano reinforced group (containing 0.5 to 3 parts of KH-550 modified nano titanium dioxide, 0.025 to 0.6 part of cerium dioxide and 0.5 to 3 parts of boron nitride) and 62 to 71 parts of an auxiliary agent group. The preparation method comprises the following steps: 1) taking diphenyl ether, paraphthaloyl chloride and isophthaloyl chloride as monomers, and synthesizing titanium modified polyether ketone ketone resins with different viscosities through segmented polymerization (1.5-2.0 hours or 3.0-4.0 hours); 2) respectively preparing a smooth bottom layer water dispersion slurry and a wrinkled surface layer water dispersion slurry; and (3) forming a compact bottom layer and a micro-wrinkle surface layer on the base material by adopting a layered spraying and stepped sintering process (280-320 DEG C, 10-20 minutes). The whole system of the coating is fluorine-free and has temperature resistance gt; the coating has the characteristics of high temperature resistance (350DEG C), wear resistance (Taber wear rate of 3-5mg / 1000r), non-sticking (contact angle gt, 100 DEG C) and heavy corrosion resistance, and is suitable for cooking utensils and chemical equipment.

S-Beta-hydroxybutyric acid compositions for oral delivery are effective in rapidly raising blood ketone levels without causing acute acidosis or gastrointestinal (GI) distress when consumed in sufficiently dilute form and / or as a gel or suspension. By limiting added beta-hydroxybutyrate salts containing alkali or alkaline earth metal ions, beta-hydroxybutyric acid solutions, gels, or suspensions can deliver exogenous ketone bodies without significantly altering electrolyte balance. Although aqueous beta-hydroxybutyric acid solutions are moderately acidic with a pH of about 3.5 to 4, when diluted with sufficient water, the water acts as a pseudo buffering agent that offsets otherwise harsh acidic effects when consumed orally. Gels and suspensions can also ameliorate acidic effects by partially encapsulating the beta-hydroxybutyric acid. Beta-hydroxybutyric acid can be pure S-beta-hydroxybutyric acid or a non-racemic mixture enriched with S-beta-hydroxybutyric acid relative to R-beta-hydroxybutyric acid.

The invention provides a preparation method of a bexagliflozin intermediate, and relates to the technical field of organic synthesis. The preparation method provided by the invention comprises the following steps: S1, substitution reaction: under the action of alkali, carrying out substitution reaction on 2-(cyclopropoxy) ethanol and a compound III ((5-halogen-2-chlorphenyl) (4-halophenyl) ketone) to generate a compound II; s2, reduction reaction: under the action of lewis acid, carrying out reduction reaction on a reducing agent and a compound II ((5-halogen-2-chlorphenyl) (4-(2-(cyclopropoxy) ethyoxyl) phenyl) ketone) to generate a compound I; the method has the advantages of mild reaction conditions, high atom utilization rate, high yield, high product quality and the like.

The invention belongs to the technical field of fine chemical engineering, and particularly discloses a method for preparing a broad-spectrum bactericide 2-n-butylbenzo [d] isothiazole-3 (2H)-ketone by a molecular editing method. The preparation method comprises the following specific steps: taking 3H-1, 2-benzodisulfophenol-3-ketone and n-butylamine as raw materials, taking Selectfluor as an additive, adding the raw materials and the additive into a mixed solvent, and carrying out heating and stirring reaction, so as to obtain the target product 2-n-butylbenzo [d] isothiazole-3 (2H)-ketone (BBIT). The method is simple and convenient to operate, the raw materials are easy to obtain, the yield is high, thiophenol raw materials or excessive alkali are prevented from being used, and potential application value is achieved.

The invention provides a high-performance concrete anticorrosive paint and a preparation method of a coating, and relates to the technical field of building materials and corrosion prevention. The coating is composed of a component A and a component B, the component A comprises epoxy resin, a composite solvent, an organic solvent, a dispersant, fumed silica and a leveling agent, and the component B comprises an epoxy hardener, a conductive polymer dispersion liquid and an organic solvent. The composite solvent is formed by compounding one or more of orthotitanate, phosphate and orthosilicate with an ester, ketone, alcohol, aromatic hydrocarbon, aliphatic hydrocarbon or ether organic solvent. The preparation method of the anticorrosive coating comprises the following steps: preparing the component A and the component B, mixing to form a coating, applying the coating to the surface of concrete, and curing. The coating is compact in structure and strong in adhesive force, can obviously improve the durability and corrosion resistance of concrete in extreme environments such as high salinity and high acid, and is particularly suitable for infrastructure protection in coastal and heavy corrosion industrial areas.

The invention discloses an isothiazolinone non-curing coating and a preparation method thereof, and relates to the technical field of waterproof coatings. The coating comprises a base material, a compound isothiazolinone antibacterial agent, a mixed stabilizer, a compound plasticizer, a compound anti-aging agent, a filler, an adhesion promoter and a solvent, the compound type isothiazolinone antibacterial agent is prepared by mixing and compounding 2-methyl-4-isothiazolin-3-ketone and 5-chloro-2-methyl-4-isothiazolin-3-ketone according to a mass ratio of (1 to 3): 1, and the compound type isothiazolinone antibacterial agent is prepared by mixing and compounding 2-methyl-4-isothiazolin-3-ketone and 5-chloro-2-methyl-4-isothiazolin-3-ketone and 5-chloro-2-methyl-4-isothiazolin-3-ketone; the mixed stabilizer is formed by mixing organic bentonite, polyamide wax and fumed silica; the defects that an existing non-curing coating is poor in antibacterial performance, insufficient in aging resistance and poor in formula compatibility are overcome.

The invention relates to the technical field of energy storage safety, and particularly discloses flame-retardant cooling liquid, a preparation method of the flame-retardant cooling liquid, an immersed energy storage device, a data center and electric equipment. According to the present invention, the base oil is at least one of the liquid halogenated alkane containing 2-6 carbon atoms, the liquid halogenated olefin, the liquid halogenated ketone and the liquid halogenated cycloalkane containing 3-6 carbon atoms, such that the high biodegradability of the base oil is maintained, the system viscosity is effectively reduced, the heat dissipation performance is improved, the insulating property of the base oil is significantly improved, and the service life of the base oil is prolonged. Meanwhile, the flame retardance is further enhanced. Therefore, the heat management efficiency of the cooling liquid is remarkably improved while environmental protection and safety are considered, and the cooling liquid has a good application prospect.

The invention discloses a self-repairing composite floor for a clean room and a preparation method of the self-repairing composite floor, and the preparation method comprises the following steps: carrying out amination treatment on nano silicon dioxide and carbon quantum dots by using a silane coupling agent, and sulfonating polyethersulfone ketone by using concentrated sulfuric acid; the preparation method comprises the following steps: carrying out curing treatment on epoxy resin, an amine curing agent, N-hydroxyethyl maleimide and tetrakis (3-mercaptopropionic acid) pentaerythritol ester to obtain epoxy-mercaptan resin; the preparation method comprises the following steps: carrying out prepolymerization reaction on vacuum dehydrated polyester polyol, tetrahydroxyethyl ethylenediamine, furanpropanol, diisocyanate, a catalyst, 2, 2 '-thiodiethanol and hydroxyl silicone oil to obtain a star-shaped polyurethane prepolymer, adding epoxy-thiol resin, glyceryl borate, sulfonated polyethersulfone ketone, aminated silicon dioxide, aminated carbon quantum dots and an auxiliary agent, carrying out ultrasonic treatment, and carrying out drying to obtain the star-shaped polyurethane resin. The self-repairing coating material is obtained; and coating the self-repairing coating material on the surface of a base plate, and performing hot-pressing curing molding to obtain the self-repairing composite floor for the clean room.

The invention belongs to the technical field of organic synthesis, and relates to a preparation method of 5, 5-dimethyl-4, 5-dihydroisoxazole. The method comprises the following steps: (1) reacting isopentenal with an oximation agent to obtain a reaction solution containing isopentenal oxime; (2) dropwise adding the reaction liquid into a mixture containing isopentenal and an acid catalyst for reaction to obtain a product; or when the reaction liquid contains water, performing phase splitting on the reaction liquid to obtain an organic phase, and dropwise adding the organic phase into a mixture containing the isopentenal and the acid catalyst for reaction to obtain a product. The method does not produce ketone by-products, and is good in atom economy, high in reaction yield, good in technological process continuity, low in cost, few in materials, simple to operate, mild in reaction condition, low in requirements on production equipment and suitable for large-scale industrial production.

The invention discloses a preparation method of polyetherketoneketone, polyetherketoneketone and application. The method comprises the following steps: (1) mixing raw materials at a first temperature, the raw materials comprising acyl chloride, a solvent, Lewis base, diphenyl ether and Lewis acid, carrying out heat preservation, heating to a second temperature, and carrying out a first reaction stage; (2) heating to a third temperature for reaction, and carrying out a second reaction stage; (3) adding a terminator into the reaction mixture in the step (2); the heating rate in the step (1) and the heating rate in the step (2) are respectively and independently 0.1-5 DEG C / min, the weight-average molecular weight of the polyetherketoneketone prepared by the method is 5000-200000, and the molecular weight distribution coefficient is 2.5-4.5. The polyetherketoneketone with relatively narrow molecular weight distribution is obtained through an electrophilic substitution path.

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

The invention belongs to the technical field of catalyst preparation, and discloses an activated carbon supported metal catalyst based on ammonia-assisted microwave reaming as well as a preparation method and application of the activated carbon supported metal catalyst. According to the activated carbon supported metal catalyst prepared through an ammonia water complexing route, metal ions can be more uniformly dispersed on an activated carbon carrier, the average size of particles is smaller, the dispersity of metal particles on the surface is high, and the catalyst has good catalytic activity. The metal precursor is dissolved in ammonia water, so that the defect of poor water solubility of partial metal is overcome, and the universality of catalyst preparation is expanded. Microwave heating is adopted for roasting and reduction, so that the catalyst preparation time is greatly shortened, and the energy consumption is reduced. In addition, the ammonia-assisted impregnation process is combined, the content of mesopores and macropores in the activated carbon metal catalyst is obviously increased, and a good pore expanding effect is achieved. The activated carbon supported metal catalyst shows better activity, selectivity and stability in high-carbon ketone synthesis reaction.

The invention provides immobilized ketoreductase, an immobilization method and application of the immobilized ketoreductase in preparation of a key intermediate of bentonatate, the amino acid sequence of the ketoreductase is as shown in SEQ ID NO.2, preferably a ketoreductase mutant is as shown in SEQ ID NO.16, and the immobilized ketoreductase comprises resin and corresponding ketoreductase. The ketoreductase mutant and the immobilized ketoreductase prepared from the ketoreductase mutant are very high in enzyme activity during ketoreduction reaction, and when the ketoreductase mutant is used for preparing a key intermediate of bentonamate, a solvent is pure water, so that the ketoreductase mutant and the immobilized ketoreductase prepared from the ketoreductase mutant are environment-friendly. The immobilized transaminase is high in conversion rate, good in stereoselectivity, good in stability, reusable and simpler to operate, so that the production cost is reduced, and industrial production is facilitated.

The invention discloses bio-based flame-retardant polyol as well as a preparation method and application thereof. Comprising the following steps: generating bio-based polyol containing 3-5 hydroxyl functionalities from raw cardanol and hydroxy ketone under the catalysis of strong acid ion exchange resin, and reacting with bromine to generate the bromine-containing bio-based flame-retardant polyol. The bio-based polyol prepared by the method is good in flame retardant property, a carbamate bond generated by a phenolic hydroxyl group and isocyanate can be reversibly decomposed at a relatively low temperature, and the bio-based polyol has good recycling performance and high bio-based content and is a green and environment-friendly bio-based material.

The invention discloses an alcohol dehydrogenase mutant for high yield of tea flavor ketone and application of the alcohol dehydrogenase mutant in a one-pot method. The mutant is A182L or A182L / V214T. The alcohol dehydrogenase mutant has high catalytic activity on 4-hydroxyisophorone, and the yield of tea flavor ketone prepared by catalysis of the mutant A182L / V214T can reach 97% and is 3.73 times that of an original enzyme; the alcohol dehydrogenase mutant has high catalytic activity of synthesizing the tea aroma ketone through one-pot catalysis of isophorone, and the yield of the tea aroma ketone obtained through direct oxidation of isophorone by jointly using the mutant A182L / V214T and a cytochrome P450BM3 monooxygenase mutant can reach 92%; the alcohol dehydrogenase mutant has the advantages of simple production process, mild reaction conditions and environment-friendly production process, is beneficial to the industrial production of the tea flavor ketone, and has wide application prospects.

The invention relates to the technical field of waste gas treatment, and particularly discloses waste gas treatment liquid for treating large-air-volume low-concentration waste gas through a water-based method. The waste gas treatment liquid for treating the large-air-volume low-concentration waste gas through the water-based method comprises a surfactant, a defoaming agent, a dissolution accelerant and water. Wherein the surfactant can be selected from any one or more of polyoxyethylene alkyl ether, polyoxyethylene alkyl ether and polyoxyethylene fatty acid ester; the dissolution accelerant can be selected from any one or more of ethylene glycol monobutyl ether, diethylene glycol monobutyl ether and triethylene glycol monobutyl ether; the defoaming agent is any one or more of butanol, dimethyl silicone oil, silicone and polyether modified polysiloxane. When the waste gas absorption liquid obtained in the invention is used for treating waste gas, the absorption efficiency of methanol, butanol, benzene, toluene, xylene, ethyl acetate, dichloromethane and acetone is obviously improved, and the absorption efficiency of the waste gas absorption liquid on aromatic hydrocarbon, halogenated hydrocarbon, alcohol, ketone and ester pollutants is improved.

The application discloses a kind of hydrolysis-resistant acetylacetamide modified polyvinyl alcohol and preparation method thereof, and the preparation method comprises the following steps: double vinyl ketone and first and alcohol amine compound are reacted to generate N-(hydroxyalkyl) acetylacetamide intermediate;Then trichloro cyanogen and N-(hydroxyalkyl) acetylacetamide intermediate are reacted to generate 3,5-bis[acetylacetamide alkoxyl] monochloro s-triazine;Finally, 3,5-bis[acetylacetamide alkoxyl] monochloro s-triazine is reacted with PVA in polar solvent to generate AAM-PVA.The AAM-PVA prepared in the application can be used as a protective colloid for polyvinyl acetate emulsion polymerization, and the prepared emulsion adhesive has obvious improvement in water resistance, tensile strength and stability;The raw materials of the application are cheap and easy to obtain, the preparation process is simple, the reaction conditions are mild, and there is no waste water and waste gas emission.

The invention discloses a preparation method of ethyl 4-chloroacetoacetate, and belongs to the technical field of compound synthesis. The method comprises the following steps: by taking diketene as a raw material, adding a polymethylsilsesquioxane polymerization inhibitor into a dichloromethane solvent, introducing chlorine at low temperature, carrying out chlorination reaction to generate 4-chloroacetoacetic acid, then esterifying the 4-chloroacetoacetic acid with absolute ethyl alcohol to obtain a crude product, and finally distilling and purifying to obtain the product. The preparation method is characterized in that a polymethylsilsesquioxane polymerization inhibitor is added before chlorination reaction, the polymerization inhibitor is prepared by grafting a functional monomer containing a 3, 5-di-tert-butyl-4-hydroxycinnamic acid structure onto surface-ethenylated polymethylsilsesquioxane microspheres, and the polymethylsilsesquioxane polymerization inhibitor has both steric hindrance and free radical capture capability. The method can effectively inhibit the self-polymerization and copolymerization tendency of diketene, intermediates and products in a reaction system, obviously reduces the generation of by-products such as dichloro and polychloro, enables the product to be high in yield and good in purity, and meets the quality requirements of high-end medical intermediates.

The utility model discloses post-treatment equipment for 2, 2-dimethylpiperidine-4-ketone production, which belongs to the technical field of waste gas treatment and comprises a pretreatment unit, a microwave catalytic oxidation unit, an adsorption unit, a condensation unit and a discharge system. The pretreatment unit comprises multiple layers of filter screens; the microwave catalytic oxidation unit comprises a catalysis box, and a microwave generator is arranged in the catalysis box; the adsorption unit comprises an adsorption cavity, an air uniformizing plate is arranged above the adsorption cavity, and a plurality of layers of activated carbon adsorption beds are arranged below the air uniformizing plate; the condensing unit comprises a condenser and a heat removal fan; the exhaust system comprises an exhaust funnel, and the exhaust funnel is provided with a gas monitor and an exhaust valve. Particulate matters in waste gas are removed through the pretreatment unit, catalytic oxidation is performed through the microwave catalytic oxidation unit, harmful components are further removed through an activated carbon adsorption bed of the adsorption unit, the condensation unit is used for cooling the waste gas and promoting VOCs to be condensed into liquid, and finally the treated waste gas is discharged through the discharge system.

The invention discloses zwitterionic concrete internal curing hydrogel based on humidity-pH dual responsiveness and a preparation method of the zwitterionic concrete internal curing hydrogel, and belongs to the technical field of building materials. The water-based cleaning agent is prepared from the following raw material components in percentage by weight: 6%-8% of N-vinyl imidazole, 8%-12% of 2-methylimidazole, 6%-8% of 2-acrylamido-2-methylpropanesulfonic acid, 2%-4% of sodium p-styrenesulfonate, 26%-30% of acrylic acid, 18%-21% of N-vinyl pyrrolidone, 15%-18% of glycidyl methacrylate, 2%-5% of nano montmorillonite powder, 0.05%-0.1% of divinyl benzene, 0.05%-0.15% of N, N-dimethylformamide and the balance of water. The invention discloses an anti-freezing agent which is prepared from the following components in percentage by weight: 0.1%-0.3% of N, N-methylene bisacrylamide, 0.1%-0.3% of 1-[4-(2-hydroxyethoxy)-phenyl]-2-hydroxy-2-methyl-1-propane-1-ketone, 0.5%-0.8% of ammonium persulfate and 0.5%-0.8% of sodium hydrogen sulfite. Double response to the internal humidity and pH value of the concrete can be achieved, and the requirement for precise internal curing of modern high-performance concrete is met.

Methods and systems for converting a renewable fuel intermediate composition to finished transportation fuel are provided herein. In some examples, a renewable fuel intermediate composition is flowed over a first catalyst in a first reaction zone to generate a saturated, hydrodeoxygenated product. A liquid portion of the renewable fuel intermediate composition may be characterized as having more than about 70 wt % of the oxygen being within ketone groups. The saturated, hydrodeoxygenated product may be flowed over a second fixed-bed catalyst in a second reaction zone to generate a product including the finished transportation fuel.

The invention relates to the technical field of biology, in particular to a carbonyl reductase mutant, a gene, an engineering bacterium and application. The amino acid sequence of the carbonyl reductase mutant is shown as SEQ ID NO: 1, the catalytic efficiency of asymmetric reductive hydrogenation of prochiral ketone compounds is improved, the stereoselectivity of chiral hydroxyl compounds formed through catalysis is improved, and the synthesis efficiency of (S)-1-(5-fluoro-2-iodophenyl) ethanol is improved.

The invention belongs to the technical field of fermentation engineering, and particularly relates to a staphylococcus pseudoxylosus strain and application of the staphylococcus pseudoxylosus strain in enhancing the flavor of fermented food, and the preservation number of the staphylococcus pseudoxylosus strain is GDMCC NO: 66815. The strain can produce lipase and protease, and can significantly enhance the content of flavor substances such as ketones, alcohols, esters, pyrazine furans and the like in fermented food. And inoculating the staphylococcus pseudoxylosus E2 into food to be fermented, and fermenting at 25-40 DEG C for 5-35 days. Compared with natural fermentation, the content of flavor substances in fermented food can be remarkably increased, and the method is suitable for commercialization.

The invention belongs to the field of batteries, and particularly discloses a battery positive electrode and a zinc-iodine battery containing the battery positive electrode. The battery positive electrode comprises a positive electrode material layer, and the positive electrode material layer contains a positive electrode material; the positive electrode material contains an active substance and a polar organic catalyst; the polar organic catalyst contains at least one group selected from hydroxyl, carboxyl, aldehyde group, ketone group, ester group, ether group, amino, amide group, nitryl, nitrile group, sulfonic acid group and quaternary ammonium salt. The polar organic catalyst is introduced into the battery positive electrode, the contained polar group can efficiently catalyze the iodine positive electrode four-electron conversion reaction, the reaction kinetics of the battery system is obviously accelerated, the iodine positive electrode capacity multiplication is realized, the complete conversion of I0 / I + can be realized, and the high-voltage platform capacity ratio reaches 50%; and the iodine positive electrode capacity, the rate capability and the self-discharge capacity retention rate of the zinc-iodine battery containing the battery positive electrode are remarkably improved.

The invention discloses a ketoazine-based polymer, an anion exchange membrane and a preparation method and application of the ketoazine-based polymer and the anion exchange membrane. A first linking group and a second linking group are mixed and then mixed with an aryl monomer A in an aprotic solvent of halogen atoms; slowly adding a super acid mixture; performing polymerization reaction in an environment of-5 to 3 DEG C to obtain a reaction solution; pouring the reaction liquid into a first mixed solvent to obtain PAAz; carrying out primary quaternization reaction on PAAz through carbonate, bicarbonate or hydroxide salt of alkali metal, and adding an organic base catalyst to assist the primary quaternization reaction; in the first quaternization reaction, a quaternization reagent is added; and pouring into a second mixed solvent, and precipitating to obtain purified PAAz. Under the condition of super acid catalysis, two or more alicyclic amine derivatives containing ketone groups react with one or more aromatic fused rings to generate a polymer containing secondary or tertiary amine. And carrying out quaternization treatment to finally form the cationic polymer.

The invention relates to a method for preparing ketoxime compounds, which comprises the following steps: contacting a ketone compound, a catalyst and an ammonia source in a liquid-phase medium to obtain a reaction mixture, and releasing ammonia gas from the ammonia source; the catalyst comprises a carrier and active metal loaded on the carrier, the active metal comprises IB group metal and VIII group metal, and the carrier comprises a titanium silicalite molecular sieve; introducing the first raw material gas and the second raw material gas into the reaction mixture to be in contact with a catalyst for in-situ reaction to obtain a reaction product containing the ketoxime compound; wherein the first feed gas comprises hydrogen, and the second feed gas comprises oxygen. According to the method, hydrogen and oxygen are used as reaction raw material gases, ketoxime is prepared through in-situ ammoximation of ketone compounds, the safety problem caused by production, use, storage and transportation of hydrogen peroxide is solved, and the method is simple in process and environmentally friendly.

The invention relates to the technical field of comprehensive treatment of agricultural pests, and particularly provides a bactrocera cucurbitae double-trapping type attractant based on optimal matching of host and intestinal bacteria volatile matters and application of the bactrocera cucurbitae double-trapping type attractant. The attractant comprises an active component and a synergistic component, the active component is derived from balsam pear and towel gourd volatile matters and bactrocera cucurbitae intestinal bacterial metabolites, and comprises 2-methyl ethyl valerate, propyl hexanoate, ethyl hexadienoate, heptanal, benzyl alcohol, 3-methyl acetic acid-1-butanol, indole and 1-undecanol; and the synergistic component is myzobenzoic ketone. Active components are quickly released in the early stage of application, so that the attraction efficiency is remarkably improved; the synergistic component prolongs the trapping lasting period through the slow release effect, and the long-term trapping effect is ensured. All the components of the attractant provided by the invention are biological sources or environment-friendly chemical substances, the attractant meets the requirement of green prevention and control, can efficiently attract male and female adults at the same time, makes up the limitation that a traditional sex attractant only induces male adults or a food attractant only induces female adults, and is beneficial to more comprehensive control of population quantity.