6064 results about "Solvent" patented technology

The invention relates to a preparation method of phenylmethylamine. The technical scheme adopted by the invention for mainly solving the problems of high catalyst loss, low production efficiency and high intermittent operation labor intensity is as follows: the preparation method of the phenylmethylamine comprises the following steps: mixing the raw material of cyanobenzene with a solvent material or at least one of one part of product materials in a mixing unit, introducing the mixture into a fixed bed hydrogenation reactor to be in contact with hydrogen and a catalyst and carry out multi-phase continuous hydrogenation reaction to obtain a product material containing phenylmethylamine, separating the product material to obtain a phenylmethylamine product, wherein the catalyst is a metal loaded catalyst; and the metal is selected from at least one of Pd, Pt, Cu, Ni, Mo and Fe. The preparation method can be used for preparing phenylmethylamine.

The invention discloses a self-crosslinking temperature-resistant salt-resistant emulsion type fracturing fluid thickening agent and a preparation method thereof, and belongs to the technical field of oilfield chemistry. The raw materials adopted by the invention comprise 30 to 50 parts of an oily solvent, 15 to 25 parts of deionized water, 10 to 20 parts of acrylamide, 5 to 10 parts of acrylic acid, 2 to 4 parts of 2-acrylamido-2-methylpropanesulfonic acid, 0.05 to 0.2 part of a crosslinking monomer, 0.5 to 1 part of a quaternary ammonium salt type hydrophobic association monomer, 4 to 8 parts of an emulsifier and 1 to 2 parts of a phase inversion agent. The self-crosslinking emulsion is formed through water phase-oil phase mixing, high-speed emulsification, low-temperature initiation polymerization and phase inversion treatment. Based on physical-chemical double-crosslinking temperature control cooperation, a salt-resistant-hydrophobic double-shielding mechanism and an integrated design without an exogenous crosslinking agent, the contradiction between the temperature-resistant and salt-resistant performance of a traditional thickening agent and the process complexity is broken through, and a technical support is provided for efficient development of high-temperature and high-salt oil and gas reservoirs.

The invention relates to a preparation method of Pt monatomic nano-enzyme and application of Pt monatomic nano-enzyme in cardiac troponin I. The preparation method comprises the following steps: 1) ultrasonically dispersing cobalt salt, selenium powder, chloroplatinic acid, urea and sodium chloride in an alcohol solvent, heating and stirring until the solvent is completely volatilized to obtain a solid mixture, and grinding the solid mixture into powder; and 2) placing the powder in a heating device, carrying out Joule heat treatment in an air atmosphere, washing a reactant, and carrying out vacuum drying to obtain the Pt monatomic nano-enzyme. Se doping is introduced in the one-step chemical reaction process to construct oxygen vacancies, rapid heating and structural shaping are achieved in combination with Joule heat treatment, the Se-doped Co3O4-loaded Pt monatomic catalyst is obtained, the oxygen vacancies and Se doping sites are synergistically used as anchoring sites, Pt monatomic atoms are effectively fixed, and the loading capacity and dispersity of the Pt monatomic atoms are improved. The obtained material shows excellent POD-like enzyme activity, can be used for constructing a high-sensitivity colorimetric immunoassay system, and realizes rapid and accurate detection of cTnI.

The invention provides an intelligent evaluation method and system for the antibacterial effect of a water matrix standard substance, and relates to the technical field of intelligent evaluation, and the method comprises the following steps: preparing a bacterial suspension in a logarithmic phase and checking turbidity; preparing a water matrix standard substance and a control solvent, and obtaining a baseline parameter set; setting inoculum size and incubation conditions, determining the antibacterial efficiency in parallel, and performing image segmentation correction on sticky colonies to obtain an original observation set; establishing a deviation transfer relationship, correcting the original data, and forming an endpoint quantization set; and the bacteriostatic validity is output through evidence fusion, and a supplementary experiment is carried out on a critical condition. According to the method, the accuracy and reliability of bacteriostatic effect evaluation of the water matrix standard substance are improved.

The invention discloses a lubricant composition and application thereof in processing of a high-weather-resistance PC hollow plate, and relates to the technical field of lubricant compositions. The lubricant composition comprises the following components in parts by mass: 40-60 parts of base oil, 5-15 parts of a weather-resistant stable additive, 3-8 parts of an anti-wear reagent at extreme pressure, 2-6 parts of a dispersing agent, 1-4 parts of an antioxidant, 0.5-2 parts of a coupling agent and 20-30 parts of a solvent. Through the molecular collaborative design of the polar base oil and the solvent, the thermal decomposition tendency in the processing process is remarkably reduced, and a lubricating system is promoted to be upgraded to a low-volatilization and low-pollution green process direction. A weather-resistant additive molecular skeleton with anti-oxidation and anti-ultraviolet characteristics is innovatively constructed, integration of multiple protection mechanisms in material processing and service stages is realized, and dependence on secondary addition of auxiliaries in a traditional process is reduced.

The invention provides a thermal interface material based on vinyl imidazole ionic liquid as well as a preparation method and application of the thermal interface material. The thermal interface material is prepared from the following raw materials: the vinyl imidazole ionic liquid, a heat-conducting filler subjected to surface treatment by a silane coupling agent, an initiator and a cross-linking agent. The thermal interface material is based on the vinyl imidazole ionic liquid and the heat-conducting filler, the limitation of a traditional thermal interface material base body is broken through, dispensing can be achieved, no solvent is needed in the preparation process, the adverse effect of solvent residues on the performance of a chip when the thermal interface material is applied to the chip subsequently can be avoided, and the thermal interface material has ideal interface bonding strength; the heat conduction effect is remarkable and stable, the heat stability is good, the material can be well attached to an interface, the problems of stress concentration, cracks and the like are not prone to occurring, and the material can be widely applied to the heat conduction and heat dissipation fields of aerospace, advanced energy, electronic information, military industry and the like.

The invention is about a method of marking ink which is only used to defend fake. The composition of it is: lipidol or lipid, surface active agent, integration agent, water, buffering agent. Their mass percents are: 1,2-hexylene glycol: 5%-15%, butanol: 1-5%, DH-1: 5-10%, EDTA: 0.1-0.5%, MS-1: 0.1-1%, water: the rest. The process is: a. dissolving the colorant in water, b. put the correct percent of 1,2-hexylene glycol and butanol into the solvent, then dropping the MS-1 and EDTA solution when mixing the solvent for 30-50 min, c. put the rest precent of water into the printing ink box. The picture and word would be shown red fluorescence in the UV but blank in the usual light.

The invention provides a method for synthesizing 1, 2-bis (4-vinyl phenyl) ethane, which comprises the following steps: adding a first solvent, methyl triphenyl phosphine halide and strong alkali into a reaction flask, and uniformly stirring to obtain a first mixed solution; heating the first mixed solution and carrying out reflux reaction for 1 hour; dropwise adding a 1, 2-bis (p-formaldehyde phenyl) ethane solution until the reflux reaction is finished to obtain a second mixed solution; reducing the temperature of the second mixed solution to room temperature, and adjusting the pH value of the second mixed solution to obtain a first solution; layering the first solution, and taking an organic layer; adding a polymerization inhibitor into the organic layer to obtain a second solution; concentrating the second solution to obtain a 1, 2-bis (4-vinyl phenyl) ethane crude product; adding a poor solvent into the crude product, stirring and crystallizing; filtering the crystal to obtain a filter cake, adding a second solvent into the filter cake, and washing and drying the filter cake to obtain 1, 2-bis (4-vinyl phenyl) ethane; the method for synthesizing the BVPE is simple and low in raw material cost, and the synthesized BVPE is high in purity and free of product isomeride.

The invention relates to the technical field of liquid-liquid homogeneous microextraction, in particular to a method for microextraction analysis of perfluorooctanoic acid by using a switchable eutectic solvent. Comprising the following steps: step 1, mixing a hydrogen bond acceptor and a hydrogen bond donor according to a set proportion value, and stirring and mixing at a set temperature value to obtain a eutectic solvent; step 2, filtering the water sample through a water-based filter membrane, then adding a set amount of deep eutectic solvent, dropwise adding an alkaline solution, carrying out full vortex mixing through a mixer, and then adding an acidic solution to form an emulsion; according to the method, the high selectivity of the green solvent with a specific structure on perfluorooctanoic acid and the characteristic that the solvent is switched between hydrophilic and hydrophobic forms are utilized, so that the microextraction time is shortened, and the impurity removal and enrichment effects are enhanced. The method is simple and convenient to operate, green, environment-friendly, low in cost and good in effect, has the advantage of efficiently and rapidly pretreating the batch small-size complex matrix sample, and has a relatively good application prospect.

The invention belongs to the technical field of phosphoric acid purification, and particularly relates to a removing agent and a removing method for heavy metal cadmium in phosphoric acid. The removing agent comprises a solvent, a thiophosphoric acid trapping agent A and a thiophosphoric acid trapping agent B, wherein the thiophosphoric acid trapping agent A and the thiophosphoric acid trapping agent B are dispersed in the solvent; the thiophosphoric acid trapping agent A and the thiophosphoric acid trapping agent B are different types of thiophosphoric acid trapping agents and are respectively and independently selected from one of alkyl dithiophosphoric acid or salts thereof, phenolic dithiophosphoric acid or salts thereof and amino dithiophosphoric acid or salts thereof; and at least one hydrocarbyl dithiophosphoric acid or salt thereof is selected; the salt is sodium salt or ammonium salt; the solvent is water or an alkaline aqueous solution. According to the method, a composition of a dithiophosphoric acid trapping agent is used as a removing agent for cadmium in wet-process phosphoric acid, a precipitate which is insoluble in a strongly acidic water phase is generated after reaction, and phosphoric acid cadmium removal is realized after filtration. Compared with a conventional sulfide precipitation method, the method provided by the invention has the advantages of less cadmium residue in phosphoric acid and less pollution.

Provided is a flux that can suppress the generation of voids when an indium alloy sheet is used to perform a continuous reflow under different temperature conditions. The present invention employs a flux that contains a rosin ester, an organic acid (A), and a solvent (S). The organic acid (A) includes a dimer acid (A1) that demonstrates a weight reduction rate of not more than 1 mass % in a thermogravimetric analysis in which the dimer acid is heated up to 260° C. at a temperature rising rate of 10° C. / min. The solvent (S) includes a solvent (S1) that demonstrates the weight reduction rate of at least 99 mass % in a thermogravimetric analysis in which the solvent (S1) is heated up to 150° C. at a temperature rising rate of 6° C. / min.

The invention relates to the field of foaming materials, in particular to a low-solvent-residue expandable polystyrene material and a preparation method thereof. The expandable polystyrene material with low solvent residue comprises the following raw materials in percentage by weight: 0.35-0.45% of a free radical initiation system, 0.35-0.45% of S, S, S, S, S, S, S, S, S, S, S, S, S, S, S According to the present invention, the material comprises, by weight, 0.1-0.15% of S, S '-bis (alpha, alpha'-dimethyl-alpha ''-acetoxy) trithiocarbonate, 0.15-0.2% of ascorbic acid, 0.1-0.2% of a nucleating agent, 0.2-0.3% of a suspending agent, 0.001-0.003% of an emulsifier, 5-6% of a foaming agent, 0.15-0.25% of a plasticizer, 0.001-0.002% of hydroxyethyl cellulose, 0.05% of sodium phosphate, 0.1-0.2% of zinc stearate, and 0.1-0.2% of glyceryl stearate, the obtained material has low solvent residue, meets food safety requirements, and is suitable for food packaging.

The invention belongs to the technical field of medical and mechanical combinations, and discloses a high-permeability and low-sensitivity ripdicaine wound patch and a preparation method thereof.The high-permeability and low-sensitivity ripdicaine wound patch comprises a wound patch body, and the wound patch body is prepared from, by mass, 0.1%-0.4% of sodium hyaluronate, 1.5%-3.5% of lidocaine, 1.5%-3.5% of prilocaine, 3%-10% of solvent, 0.5%-8% of emulsifier, 2%-10% of humectant, 0.1%-5% of soothing agent, 0.1%-1.5% of stabilizer, 0.1%-1% of thickener and the balance water. According to the present invention, the total amount of the raw materials is 100%, the total amount of the raw materials is 100%, the total amount of the raw materials is 100%, the total amount of the raw materials is 100%, the total amount of the raw materials is 100%, the total amount of the raw materials is 100%, the total amount of the raw materials is 100%, the total amount of the raw materials is 100%, and the total amount of the raw materials is 100%. And the anesthetic has the advantages of quick effect taking, low sensitivity, capability of resisting moist heat sterilization and good stability.

The invention provides an antifouling self-cleaning fluorocarbon finish paint as well as a preparation method and application thereof, and particularly relates to the technical field of special coatings. The antifouling self-cleaning fluorocarbon finish paint is composed of a component A and a component B in a ratio of (80-87): 16, the component A is prepared from the following components in parts by weight: 560 to 580 parts of fluorocarbon resin, 30 to 35 parts of a first solvent, 20 to 40 parts of a second solvent, 180 to 220 parts of titanium dioxide, 90 to 110 parts of filler, 11 to 20 parts of a light stabilizer, 3 to 5 parts of a thickening agent and 13 to 28 parts of an auxiliary agent; the component B comprises the following components in parts by weight: 20-22 parts of fluorocarbon resin, 4-5 parts of a chain extender, 15-20 parts of a diamine curing agent, 15-20 parts of a polyamine curing agent and 25-35 parts of a second solvent. According to the finishing paint, on the basis of enhancing the self-cleaning capability, the weather resistance of a coating is improved, and the aging and damage of the coating are delayed, so that the service life of the coating is prolonged.

The invention provides an SSZ-13 molecular sieve as well as a preparation method and application thereof, the preparation method comprises the following steps: mixing activated silica-alumina minerals, SSZ-13 seed crystals, a silicon source, a template agent and a second alkali source to obtain dry glue, and then carrying out crystallization treatment on the dry glue in the presence of water vapor to obtain the SSZ-13 molecular sieve. According to the preparation method, a solvent is not adopted, a small amount of deionized water is used for providing a steam phase, the utilization rate of the raw materials can be increased, the high solid yield is obtained, the loss of a solid phase is reduced, no alkaline wastewater is generated, and the synthesis cost of the SSZ-13 molecular sieve is remarkably reduced. When the SSZ-13 molecular sieve prepared by the method is used for CO2 / CH4 adsorption separation, the SSZ-13 molecular sieve has relatively high separation selectivity.

The invention discloses multi-solvent synergistically activated low-temperature semi-sintered copper paste and a preparation method and application thereof, and belongs to the technical field of conductive paste. The multi-solvent synergistically activated low-temperature semi-sintered copper slurry comprises the following raw material components in percentage by mass: 82-88% of conductive filler, 2-3% of a resin carrier, 4-7% of an activating solvent, 4-7% of a dispersing solvent and 2-3% of a curing agent. Through cooperation of multiple solvents, full-stage activation of the copper particles is achieved, pre-connection and sintering of the copper particles before resin is completely crosslinked and cured are promoted, densification of the overall structure is improved, the insulation barrier effect of the resin is effectively avoided, the resistivity is reduced, meanwhile, inhibition of the resin on sintering of the copper particles is solved, and the service life of the copper particles is prolonged. And good balance between conductivity and interface adhesion is realized. Through resin curing, chemical bonding between the slurry and the substrate can be enhanced, a metal bond network among copper particles is expanded, and mechanical connection stability and electrical performance are guaranteed.

The invention discloses EVA (Ethylene Vinyl Acetate) with high molecular weight and narrow molecular weight distribution and a preparation method thereof, and relates to the technical field of EVA. According to the technical scheme, the preparation method comprises the following steps: in a protective gas atmosphere, adding vinyl acetate and a reaction solvent into a reaction kettle, introducing ethylene gas, replacing the reaction kettle with the ethylene gas environment, then adding an initiator and a molecular weight regulator, and simultaneously heating to 60-80 DEG C for reaction; after the reaction is completed, the reaction kettle is decompressed and cooled, a terminator is added for quenching reaction, and EVA with high molecular weight and narrow molecular weight distribution is obtained. According to the invention, the molecular weight of EVA is improved, and the molecular weight distribution of EVA is reduced, so that the problems of low molecular weight and wide molecular weight distribution of EVOH are solved, and the processability and mechanical property of EVOH are greatly improved.

The invention belongs to the technical field of traditional Chinese medicine detection, and discloses a detection method for a characteristic spectrum of Uighur medicine Kspecific heat extracting tablets and application of the detection method. The detection method provided by the invention comprises the following steps: preparing a test sample solution by taking a 75% methanol solution as a solvent, and determining the test sample solutions prepared from different batches of test samples by adopting ultra-high performance liquid chromatography to obtain a characteristic spectrum; the chromatographic conditions of the ultra-high performance liquid chromatography are as follows: a chromatographic column is a C18 chromatographic column, a mobile phase A is acetonitrile, a mobile phase B is a 0.1 vol% phosphoric acid solution, and the flow velocity is 0.25-0.35 mL / min; the detection wavelength is 0 to 18 minutes, and the wavelength is 327 nm; the time is 18 to 28.5 min, and the wavelength is 254 nm; when the time is 28.5 to 37.6 minutes, the wavelength is 242 nm; after 37.6 to 70 minutes, the wavelength is 210 nm; the sample size is 1 microliter, the column temperature is 20-40 DEG C, and gradient elution is carried out. The invention provides a more scientific identification and quality control method for the Kespecific heat tablets.

A method for determining the water content of a hygroscopic fluid. The method includes inserting an amount of hygroscopic fluid into a fluid ejection cartridge; attaching the fluid ejection cartridge to a fluid ejection device; activating the fluid ejection cartridge to dispense a predetermined number of fluid droplets from one or more nozzles of an ejection head attached to the fluid ejection cartridge onto a substrate to determine a total mass of the fluid droplets dispensed, a velocity of the dispensed fluid droplets or a combination of the total mass of the fluid droplets dispensed and the velocity of the dispensed fluid droplets; and using an information database that correlates the water content of the hygroscopic fluid to an average mass per fluid droplet dispensed and the velocity of the fluid droplets dispensed to determine the water content of the hygroscopic fluid.

The invention relates to the technical field of waterproof materials, and particularly discloses a high-elasticity waterproof emulsion and a preparation method thereof. The invention discloses a high-elasticity waterproof emulsion. The water-based paint is prepared from the following raw materials in parts by mass: 40 to 60 parts of modified acrylic resin emulsion, 25 to 40 parts of waterborne polyurethane, 3 to 6 parts of hydroxyethyl methylacrylate, 0.5 to 1 part of mercaptopropionic acid, 6 to 8 parts of fluorinated mica sheet, 3 to 6 parts of organic silicon emulsion, 2 to 4 parts of fluorocarbon surfactant, 0.8 to 1.5 parts of adipic dihydrazide, 0.3 to 0.8 part of dynamic cross-linking agent, 3 to 8 parts of compatilizer, 0.5 to 1 part of antioxidant, 0.5 to 1 part of anti-aging agent, 0.5 to 1.5 parts of defoaming agent and 40 to 55 parts of solvent. The modified acrylic resin emulsion is prepared from a monomer comprising diacetone acrylamide. The high-elasticity waterproof emulsion prepared by the invention has relatively good elasticity, waterproof performance and aging resistance.

The invention belongs to the technical field of oil well paraffin removal and prevention, and relates to a paraffin removal and prevention agent for a shale oil shaft and a preparation method thereof. The paraffin remover and inhibitor for the shale oil wellbore comprises the following raw materials in percentage by mass: 40-55% of an oily solvent, 1-3% of a cosolvent, 1-2% of imidazole bis (trifluoromethanesulfonyl) imide salt, 10-20% of a wax crystal modifier, 3-5% of an emulsifier, 1-2% of an alkaline regulator and 25-35% of water, wherein the sum of the mass percentages of the raw materials is 100%. The wax crystal modifier is prepared by copolymerizing (methyl) acrylic acid C12-C16 ester, (methyl) acrylic acid C1-C3 ester and (methyl) acryloyl chloride and then reacting with C20-C30 alkyl alcohol. The wax crystal modifier provided by the invention has long-medium-short branched chains, and interacts with the imidazole bis (trifluoromethanesulfonimide) salt capable of improving the paraffin removal effect and low-temperature fluidity, so that the efficient paraffin removal and inhibition effect is realized, and the better paraffin removal and inhibition effect can still be kept at low temperature.

The invention relates to the technical field of fluorination processes, in particular to a purification method of a high-purity fluorocarbonate-based solvent, which comprises the following steps: S1, introducing fluorocarbonate-based solvent crude gas into a purification cavity, and liquefying the crude gas through a liquefaction separation module; s2, separating the liquid obtained in the step S1, conveying the separated liquid into a crystallizing pond, cooling the liquid in the crystallizing pond to enter a crystallization critical state, rotating the rotating crystal plate group in the crystallizing pond, crystallizing the liquid on the surface of the rotating crystal plate group, and continuously collecting crystals above the crystallizing pond through a collecting assembly; and S3, washing and filtering the crystals collected in S2 to obtain the high-purity fluorocarbonic ester-based solvent. According to the purification method of the high-purity fluorocarbonate-based solvent provided by the invention, crude gas is liquefied by adopting the liquefaction module, and then the liquefied liquid is continuously crystallized and collected by adopting the rotary crystallization module, so that the high-purity fluorocarbonate-based solvent can be efficiently and simply prepared, and the purification method has good industrial value.

The present invention relates to a method for quickly identifying white vaseline from different manufacturers based on silver salt-assisted laser desorption ionization-time of flight mass spectrometry, and belongs to the field of detection. Specifically comprising the following steps: S1, exploring and optimizing metal salt ion conditions, matrix conditions, and sampling methods, and using the optimized experimental conditions for sample preparation; S2, measuring the sample; S3, using eMSTAT Solution software for data analysis to achieve identification of white vaseline from different manufacturers. The method of the present invention replaces traditional organic matrices with silver salts, eliminates background interference, and improves the mass spectrometry signal-to-noise ratio; combines a direct smearing method to avoid complex solvent preparation and extraction, and is easy to operate; applies a mass spectrometer for mass spectrometry acquisition, has accurate molecular weight, reduces the detection time of each sample to 6 seconds, has high analytical throughput, and is low in cost, thereby achieving high-throughput, accurate, and rapid identification of large quantities of white vaseline from different sources.

The invention discloses a low-water-solubility medicine crystal as well as a preparation method and application thereof. The compound Z pamoate crystal form I has large characteristic diffraction peaks at one or more positions with diffraction angles 2 theta of 9.9 + / -0.2 degrees, 10.7 + / -0.2 degrees, 12.1 + / -0.2 degrees, 14.9 + / -0.2 degrees, 17.3 + / -0.2 degrees, 19.4 + / -0.2 degrees, 20.7 + / -0.2 degrees and 23.1 + / -0.2 degrees. Compared with an amorphous compound Z pamoate, the crystal provided by the invention has the advantages of good stability, no crystal transformation phenomenon, no obvious increase of related substances and low solubility; the production process is simple, only water is used as a solvent in the whole process, and no organic solvent is used; when the long-acting slow-release anti-Parkinson medicine composition is prepared from the compound Z pamoate crystal form I, the medicine encapsulation efficiency is high, the burst release is low, the composition continuously releases the medicine in vivo for more than 2 weeks, the administration frequency of a patient can be reduced, and the medication compliance is improved.

The invention relates to the technical field of chemical synthesis, and particularly discloses an alpha methyl beta phosphonate compound and a synthesis method thereof.The alpha methyl beta phosphonate compound is obtained by directly oxidizing the alpha position of aryl ketone into carbon positive and combining the carbon positive with diethyl phosphite anions under the alkaline condition by using hydrogen peroxide and iodine as oxidizing agents. The alpha methyl substituted beta phosphate ester compound can be generated by a one-step method. The method is suitable for synthesizing compounds of phosphoric acid (methyl, ethyl, propyl and the like) with different alkyl substitutes (methyl, ethyl, propyl and the like) at carbonyl alpha positions. According to the method, the alpha-methyl substituted beta phosphate compound can be synthesized only by using commercial cheap and easily available aryl ketone as a raw material, using hydrogen peroxide and iodine as oxidants and using diethyl hypophosphite as a phosphine source, and reacting in the DMSO solvent at 100 DEG C for 12 hours, so that the target product can be obtained, and the yield is excellent. Compared with previously reported methods, the method does not need low-temperature operation, is simple to operate, adopts a one-pot method, does not need a metal catalyst, and all raw materials are common bulk chemicals.

The invention belongs to the technical field of saccharomyces cerevisiae beta-glucan, and relates to a preparation method of saccharomyces cerevisiae-sourced yeast beta-glucan. The invention relates to a preparation method of saccharomyces cerevisiae-sourced yeast beta-glucan, which comprises the following steps: uniformly mixing a yeast raw material with a first solvent, and carrying out high-pressure homogenization to obtain a homogenized feed liquid; adding food-grade alkali into the homogenized feed liquid to carry out extraction reaction, centrifuging the obtained reaction extracting solution, and separating a heavy phase to obtain a heavy-phase insoluble cell wall extract; and continuously adding a second solvent for resuspension, adding a compound enzyme preparation, adjusting the pH value of the reaction system by using an acidic reagent, carrying out an enzymatic hydrolysis reaction, centrifuging after the reaction is finished, recovering a heavy phase, and drying to obtain the insoluble yeast beta-glucan dry powder. According to the preparation method of the yeast glucan, provided by the invention, the conventional preparation process flow is shortened, the environmental protection treatment pressure is greatly relieved, the production cost is effectively reduced, and the prepared yeast glucan is higher in purity and has a better industrial application prospect.

The invention discloses a mechanical force-induced fluorescence discoloration sensor material as well as a preparation method and application thereof, and relates to the technical field of organic synthesis and fine chemical engineering. The preparation method comprises the following steps: step 1, carrying out heating reaction on 4-(1, 2, 2-triphenyl vinyl) benzaldehyde, 3-(2, 2-dicyano-1-(3, 4-diaminophenyl) vinyl) benzene-1-yl and a catalyst to prepare a compound 1-1; and 2, carrying out heating reaction on the obtained compound 1-1 and methyl iodide under the action of alkali and a solvent, and analyzing and purifying to obtain a compound 1-2. The compound disclosed by the invention is low in preparation cost, simple and convenient to operate and simple in method, the compound shows the material characteristic of mechanical force-induced fluorescence discoloration and can be applied to the fields of sensors, dyes, anti-counterfeiting and the like, and meanwhile, the synthesis method can be used for synthesis in the fields of fine organic chemical engineering such as luminescent materials, printing and dyeing technologies and the like.

The invention discloses an ether polymerization inhibitor special for a butadiene extraction system and a preparation method of the ether polymerization inhibitor. The ether polymerization inhibitor comprises the following raw materials: a polymerization inhibitor intermediate, a solvent and a dispersing agent, the production process comprises the following steps: preparing a polymerization inhibitor intermediate, preparing a solvent, compounding, feeding and mixing, filtering, removing impurities and detecting. According to the method, firstly, a polymerization inhibitor 701 and diethylene glycol normal pressure etherification process is adopted, and beta-hydroxyethyl methyl ether is introduced to seal a terminal group, so that the power consumption is reduced, the generation of byproducts is inhibited, the solubility of an intermediate acetonitrile is improved to be greater than or equal to 30g / L, and the anti-interference performance is greatly enhanced; the solvent doped with a small amount of silane modified nano diatomite is prepared, impurities can be adsorbed, metal ions can be chelated, the dispersing agent can be assisted to be evenly distributed, the problems that a pure water solvent is single in function and the dispersing agent is prone to agglomeration are solved, and the polymerization inhibition efficiency and the stability of an extraction system are guaranteed.

Flue gas is compressed to high pressures, which raises the partial pressure of carbon dioxide thus facilitating its absorption into physical solvents (e.g., water, salt solutions, methanol). When added onto an existing CO2-producing process, the compression is performed using multiple stages with intercooling. After the high-pressure carbon dioxide dissolves into the physical solvent, it flows through a series of pressure letdowns using turbines that allow the dissolved carbon dioxide to evolve from the solvent. Through a series of multiple compression stages, the evolved gas is compressed for transport, utilization, or storage. The flue gas that has been scrubbed of carbon dioxide flows through a series of expanders with interheating supplied from waste heat, or the heat of compression. The process is enhanced by employing alkalis that chemically react with acid gases, such as carbon dioxide. These same CO2-capture processes can be integrated into processes that produce shaft and / or electrical power.

The invention belongs to the technical field of welding materials, and particularly relates to efficient scaling powder and a preparation method thereof. The efficient scaling powder is composed of, by mass, 4%-10% of organic acid activating agents, 1%-2% of thiourea reinforcing agents, 0.15%-0.3% of wetting agents, 0.2%-0.6% of antioxidants, 0.3%-0.5% of surfactants, 0.05%-0.2% of defoaming agents, 3%-5% of film forming agents, 10%-15% of solvents and the balance water. The prepared scaling powder has good spreadability, stability, corrosion resistance and the like.