576 results about "Hexane" patented technology

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

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

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

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

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

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

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

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

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

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

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

The invention relates to the technical field of thin-layer chromatography detection, and discloses a thin-layer chromatography detection method for free fluorine-18 in a fluorine-18 labeled radiopharmaceutical, which adopts ethyl acetate and n-hexane as developing solvents, and the volume ratio of ethyl acetate to n-hexane is (50-90): (10-50). The developing solvent with a specific volume ratio is adopted, and the two key indexes that the Rf value of the marked active ingredient in the radiopharmaceutical is smaller than 0.8 and the separation degree (the separation degree of the marked active ingredient in the radiopharmaceutical and free fluorine-18) R is larger than 1 are considered.

The invention discloses a preparation method of an antibacterial warm-keeping fabric, and relates to the technical field of textiles. When the antibacterial warm-keeping fabric is prepared, firstly, (E)-butyl-2-ene-1, 4-diamine, glyoxal, formaldehyde and butyric acid are used as raw materials to synthesize a polyimidazolium salt antibacterial agent, then the polyimidazolium salt antibacterial agent is copolymerized with polytetrahydrofuran ether glycol and diphenylmethane diisocyanate to prepare an antibacterial polyurethane spinning solution, and the antibacterial fabric is obtained through wet spinning and weaving. The preparation method comprises the following steps: reacting L-cysteine with 3-amino propyl triethoxy silane to prepare cysteamine acyl propyl triethoxy silane, reacting with formaldehyde and phosphorous acid to obtain flame-retardant modified silane, and further preparing a silicon dioxide solution from the flame-retardant modified silane and sol-gel such as methyltrimethoxysilane; finally, the antibacterial fabric is treated with a benzophenone solution and then soaked with a silicon dioxide solution, and the antibacterial thermal fabric is prepared through ultraviolet irradiation, standing gelation, aging and hexane washing. The prepared fabric has excellent antibacterial property, heat retention property and flame retardant property.

The invention discloses an ultrasonic response quaternary ammonium salt polymer antibacterial agent and a preparation method thereof. The ultrasonic response quaternary ammonium salt polymer is prepared by the following steps: carrying out substitution reaction on azodiisobutylimidazoline and acryloyl chloride, then carrying out addition polymerization reaction with 4-aminomethylpiperidine, and then carrying out quaternization reaction with bromohexane. The obtained ultrasonic response quaternary ammonium salt polymer can be decomposed under the ultrasonic action to generate alkyl radicals, and has the sterilization effect. In addition, quaternary ammonium salt modification can improve the water solubility and the positive charge density of the polymer, and further improves the antibacterial performance.

The application discloses a method for determining 15 new psychoactive substances in saliva by solid phase supported liquid-liquid extraction (SLE) combined with ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS / MS), which specifically uses a mixed solution of methyl tert-butyl ether and n-hexane as an elution solvent, adopts solid phase supported liquid-liquid extraction to pretreat saliva samples, and then adopts UPLC-MS / MS to detect the collected eluent, so as to realize qualitative and quantitative determination of the new psychoactive substances in saliva. The method has the advantages of rapidness, accuracy, high sensitivity and simple operation, the detection limit of the method is 0.2-0.5 ng / mL, can meet the domestic and foreign limit requirements, and provides technical support for monitoring and investigation of the new psychoactive substances in saliva.

The invention provides a purification method of a naphthalimide high-purity electronic-grade photoacid generator. The method solves the problem that photo-acid cannot be purified by traditional recrystallization or directly through ion exchange columns and other methods. The method comprises the following steps: firstly synthesizing and preparing 1, 3-diketone-2-hydroxy-6-(1-hexyne) benzisoquinoline, then reacting with triethylamine and trifluoromethylsulfonyl chloride to generate a crude product 1, 3-diketone-2-(1, 1, 1-trifluoromethyl) methanesulfonic ester-6-(1-hexyne) benzisoquinoline, removing impurities from normal hexane to obtain a pure product, sublimating the material into a gas phase by using a quartz vacuum sublimation instrument, and purifying to obtain the 1, 3-diketone-2-(1, 1, 1-trifluoromethyl) methanesulfonic ester-6-(1-hexyne) benzisoquinoline. And then passing through Pure MTS9500 amino phosphonic acid type chelating resin, and finally cooling in a quartz tube to obtain the high-purity electronic-grade photoacid generator. According to the invention, the stability is high, the metal ion content is low, the purification process is convenient to process, the product is used as a photoresist-level core main material, the product is widely applied in the fields of semiconductor photoresist, other imaging systems, photocureable coatings and the like, the market scale is continuously expanded, and the product is an indispensable key material in semiconductor manufacturing and other related fields.

The invention discloses a synthesis method of mannitol carbonate sulfate, and belongs to the technical field of organic synthesis. The synthesis method provided by the invention comprises the following steps: reacting 1, 3, 4, 6-tetrachloro-2, 5-hexanediol with chlorosulfonic acid in the presence of an acid-binding agent to obtain an intermediate solution as shown in a formula (II); formula (II); and mixing the intermediate solution as shown in the formula (II) with anhydrous carbonate, heating to a first set temperature for reaction, and then heating to a second set temperature for reaction in the presence of a phase transfer catalyst to obtain the mannitol carbonic sulfate. The whole process route is short, the yield is high, and the total yield of two steps reaches 88% or above; meanwhile, few by-products are generated, the purification difficulty is low, the reaction time is short, few hazardous wastes are generated, operation is easy and convenient, and industrial large-scale production is facilitated.

The present application belongs to the field of food oil, and particularly relates to a method for processing olive oil, especially virgin olive oil. The method comprises the following steps: cleaning, drying and crushing olive pomace after oil extraction by using an organic solvent (n-hexane or ethanol), adding a certain amount of olive pomace powder into olive oil and stirring under vacuum, then removing the precipitate, and finally processing under ultrahigh pressure. The content of ethyl ester of fatty acid in the virgin olive oil processed by the method of the present application can be kept less than or equal to 35 mg / kg under the condition of 30 DEG C and packaging in the dark for 12-24 months.

The application discloses a kind of artificial cells for single-cell mass spectrometry and preparation method thereof, wherein artificial cell includes internal water phase, intermediate oil phase and external water phase;Internal water phase includes polyethylene glycol and polyvinyl alcohol aqueous solution, intermediate oil phase includes L-alpha-phosphatidylcholine chloroform and hexane mixture;External water phase includes PVA and F-68 aqueous solution.Compared with natural cell sample, the novel artificial single cell based on microfluidic self-assembly developed in the application has better uniformity, stability and controllability, effectively avoids significant measurement difference between single-cell individual samples, and effectively solves the problem of difficult stable preservation of biological samples.The proposed artificial cell preparation method will largely solve the problem of lack of standard reference material in the field of single-cell mass spectrometry, making the results of single-cell mass spectrometry method more accurate, reliable and mutually recognized.

The invention relates to the technical field of cholesterol preparation, and discloses a preparation method of plant-derived cholesterol, which comprises the following steps: 1) heating and dissolving phytosterol with n-amyl alcohol, adding stigmasterol until saturation, cooling and crystallizing, and then carrying out solid-liquid separation to obtain a stigmasterol crude product; 2) heating and dissolving the stigmasterol crude product with absolute ethyl alcohol, adding pyridine, and continuously dropwise adding acetic anhydride for reaction; after the reaction is completed, adding deionized water for mixing, extracting with n-hexane for multiple times, separating an upper-layer oil phase, and concentrating and drying the oil phase to obtain a white solid; 3, the white solid is subjected to oxidation reduction, witting reaction and hydrogenation reaction, and cholesterol is obtained.The method has the advantages that compared with the prior art that the plant source cholesterol is directly prepared from the raw material phytosterol, the process is simplified, and meanwhile the product yield can be increased.

A toner including a toner particle containing a binder resin containing an amorphous polyester A and a crystalline polyester C, and a wax, and a silica fine particle, wherein the content of the crystalline polyester C is within a specific range, the softening point of the amorphous polyester A satisfies a specific relationship, and in an X-ray diffraction spectrum under a specific temperature condition for the toner, there is a peak corresponding to the crystalline polyester C, a wax index AW1 and a crystalline polyester index AC1 of the toner satisfy a specific relationship, the silica fine particle contains a silica fine particle A having a maximum diameter of primary particle in a specific range, and the average coverages of the surface of the toner before and after the toner is treated with hexane with the silica fine particle A satisfy a specific relationship.

The invention discloses a waste offset printing ink recovery treatment method and application, and belongs to the technical field of printing ink, the recovery treatment method comprises the following steps: mixing and stirring waste offset printing ink and n-hexane through pretreatment, and removing solid-phase slag through centrifugal separation to obtain a liquid phase; concentrating the liquid phase, recovering the solvent and reserving concentrated slurry; secondly, directionally dissolving the low-molecular resin and the high-molecular resin by butyl acetate and ethylene glycol diacetate respectively through two-stage counter-current extraction and centrifugal separation to obtain a low-molecular resin solution, a high-molecular resin solution and pure pigment slurry; mixing the two resin solutions, recovering the solvent through multi-tower rectification, and refining through short-path molecular distillation to obtain regenerated resin; and finally, performing ultrasonic purification, modification and spray drying on the pigment slurry to obtain the regenerated pigment. According to the waste offset printing ink recycling treatment method and application, an efficient and reliable solution is provided for recycling of waste offset printing ink.

The invention discloses a device and a process method for separating n-hexane, acetone and chloroform by applying an extractive distillation technology to a dividing wall column, and relates to the technical field of chemical processes. The device comprises two parts: one part is an extractive distillation dividing wall tower, and the other part is a solvent recovery tower. According to the technical innovation, two extractive distillation towers in a conventional three-tower extractive distillation process are coupled into one dividing wall tower by utilizing a dividing wall tower technology, so that the dividing wall tower can be used for helping to industrially separate high-purity n-hexane, acetone and chloroform, meanwhile, the use cost of equipment is reduced, the use amount of circulating water and system heat energy is reduced, and the energy consumption is greatly reduced; and as the practicability and the economic benefit are remarkable, the method has a wide application prospect.

The application discloses a kind of efficient natamycin purification methods, comprising the following steps: taking two kinds of dichloromethane, chloroform, acetone, butanone, methanol, ethanol, petroleum ether, n-hexane are mixed to obtain mixed solution, adjust the pH of mixed solution to 6.0-7.0, then natamycin crude product is added to mixed solution and stirred into slurry;Slurry is extracted to obtain that natamycin wet product, and the natamycin wet product after extraction is washed with organic solvent;Natamycin wet product after washing is dried, and natamycin purification product is obtained.Compared with prior art, the present application optimizes the existing natamycin purification process, simplifies the natamycin purification method, reduces the production cost, improves the production efficiency, the product purity can reach more than 98%, and the product yield can reach more than 95%.The application has the advantages of less equipment investment, easy operation, less environmental pollution, simple operation, and is suitable for product industrial production.

This invention belongs to the field of lithium-ion battery flame retardant technology, specifically relating to a flame-retardant electrolyte, its preparation method, and its application. The electrolyte comprises: lithium salt, carbonate organic solvent, co-solvent, and flame-retardant additive; the concentration of lithium salt in the electrolyte composed of lithium salt and carbonate organic solvent is 0.5–5 mol / L; the volume ratio of carbonate electrolyte to flame-retardant additive is 100:(1–30); the volume ratio of co-solvent to flame-retardant additive is (4–120):(1–5); the co-solvent is a solvent capable of dissolving the flame-retardant additive, and the flame-retardant additive is a perfluorohexane derivative. This invention proposes introducing a co-solvent that does not interact with lithium ions into the electrolyte. Through the bridging effect of the co-solvent, the insoluble flame retardant is introduced into the conventional electrolyte. The flame-retardant electrolyte prepared by this method does not deteriorate its electrochemical performance due to the addition of the flame retardant, thus solving the problem of incompatibility between the flame-retardant performance and electrochemical performance of lithium-ion battery electrolytes.

The invention discloses a method for preparing industrial hexane with ultralow benzene content through pre-hydrogenation. The method comprises the following steps: light naphtha, hydrogen and a hydrogenation catalyst are subjected to a hydrogenation reaction in a hydrogenation reactor for desulfurization and dearomatization, and a first mixture is obtained; feeding the first mixture into a gas-liquid separator to respectively obtain a liquid-phase product and a hydrogen-containing gas-phase product, and separating hydrogen from the gas-phase product through a circulating hydrogen compressor for recycling; and sequentially carrying out second rectification and third rectification on the liquid-phase product to obtain a heavy component substance, and adsorbing the heavy component substance through a molecular sieve. According to the method, by means of front hydrogenation reaction and rear molecular sieve adsorption, on one hand, the reaction load of molecular sieve adsorption is greatly reduced while the reaction activity of the hydrogenation reaction is improved; on the other hand, an extracting agent does not need to be added, other gas-phase and liquid-phase components are not introduced except hydrogen, the preparation process is greatly simplified, and the benzene content in the obtained cyclohexane is smaller than 5 ppm.

The invention relates to the technical field of medical biology, in particular to application of coriaria lactone or a medicinal derivative thereof in preparation of AD (Alzheimer's disease) treatment drugs. The coriaria lactone shows unique structural activity and treatment specificity, the epoxyhexane ring structure of the coriaria lactone is a key active group and is enriched in an A beta sedimentary area through synaptic gaps, the ion disturbance range is limited in a lesion microenvironment (the radius is lt and 50 microns), and wide tissue damage caused by physical electrical stimulation is avoided. The micromolecule characteristic (LogP = 1.8) of the coriaria lactone endows the coriaria lactone with the ability of spontaneously penetrating the blood brain barrier, the onset time is shortened to the hour level from several months, and meanwhile, the risk of encephaledema is avoided. Therefore, the compound can be used for preparing the medicine for treating the Alzheimer's disease, meanwhile, a proper dosage is screened, and a foundation is laid for research on preparation of the medicine for treating the AD.

Processes for preparing seed material such as for example soy beans into protein isolates and protein concentrates are provided. An example process for preparing a soy protein isolate comprises: providing defatted hexane-free soy flour pressed from soy material such as soybeans; extracting water from the hexane-free soy flour to produce an extraction slurry; adjusting the extraction slurry to have a pH in the range of 8.0 to 8.5 by adding sodium hydroxide to the extraction slurry and holding to produce pH-adjusted slurry; applying centrifugation to the pH-adjusted slurry to separate soy flour extracts from insoluble wet soy fiber material in the pH-adjusted slurry; adding a hydrochloric acid solution to the soy flour extracts to produce a low-pH mixture having a pH of about 4.5; mildly agitating the low-pH mixture; separating the low-pH mixture into a curd and a whey; diluting the curd with water and mixing with sodium hydroxide to produce a 10% dry solids mixture having a pH of about 7.0; pasteurizing the 10% dry solids mixture using a direct steam injection heater to produce a heated slurry; and cooling the heated slurry with a flash cooling system using a vacuumed tank to produce the soy protein isolate. The process may further comprise diluting the curd with water and mildly agitating to achieve a 6% dry solids mixture; and separating the 6% dry solids mixture into a second curd and a second whey, the second curd becoming the curd used in the diluting step.

The application relates to the technical field of fluorine-containing iodoalkane preparation, in particular to a preparation method of high-carbon-number diiodoperfluoroalkane, which comprises the following steps: reacting tetrafluoroethylene and elemental iodine to generate diiodotetrafluoroethane; and under the action of a catalyst, the diiodotetrafluoroethane is subjected to telomerization reaction with tetrafluoroethylene to generate high-carbon-number diiodoperfluorobutane and diiodoperfluorohexane; and the catalyst is a metal nickel catalyst supported on silicon dioxide. The metal nickel catalyst supported on silicon dioxide is used to make the diiodotetrafluoroethane and the tetrafluoroethylene subjected to telomerization reaction to obtain diiodoperfluoroalkane with higher carbon number. The application has the advantages of simple process, low reaction temperature and the like, and can significantly improve the yield of diiodoperfluorobutane and diiodoperfluorohexane.