270 results about "Ethyl Ethers" patented technology

The invention discloses a reaction buffer solution for improving endotoxin detection sensitivity of a recombinant tachypleus amebocyte lysate, a kit containing the reaction buffer solution and application of the reaction buffer solution. The reaction buffer solution comprises the following components: a Tris-HCl buffer solution, magnesium ions, sodium chloride, cane sugar, ethylene glycol diethyl ether diamine tetraacetic acid, a nonionic surfactant and cyclodextrin or a derivative thereof. The invention also discloses a preparation method of the reaction buffer solution and a kit containing the reaction buffer solution. When the reaction buffer solution or the kit is used for detecting the endotoxin of the recombinant tachypleus amebocyte lysate, the sensitivity of the recombinant tachypleus amebocyte lysate for detecting the endotoxin can be improved by one order of magnitude, the lowest detection limit can reach 0.0005 EU / ml, the reaction buffer solution or the kit has strong anti-interference capability and short reaction time, and the detection efficiency is greatly improved.

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

The invention relates to the field of cosmetics, in particular to skin moistening oil containing a water-soluble active matter and a preparation method of the skin moistening oil. The skin moistening oil of the water-soluble active matter is prepared from the following raw materials in parts by mass: 0.1-1 part of a phase A, 3-15 parts of a phase B and 80-100 parts of a phase C, wherein the phase A is a water-soluble component, and the water-soluble component comprises one or more of deionized water, VC ethyl ether and nicotinamide; the phase B is a solvent, and the solvent comprises one or more of ethyoxyl diethylene glycol, 1, 2-pentanediol, isopentanediol and isostearic acid; the phase C is skin moistening oil, and the skin moistening oil comprises caprylic / capric triglyceride. The skin moistening oil product provided by the invention has the advantages of clear and transparent appearance, good fluidity, excellent stability, no need of adding a surfactant or a solubilizer, mildness, no irritation, simple process, controllable cost, good practical value and good application prospect.

The invention provides a nomeline nasal-brain delivery preparation for transnasal region mucosa administration, and an auxiliary material mixture of the nasal-brain delivery preparation comprises 1) phospholipid, and 2) any one of diluent ethyl oleate, isopropyl myristate, sesame oil or castor oil; optionally, the auxiliary material mixture can also comprise 3) a dissolving agent such as ethanol or diethylene glycol monoethyl ether, the auxiliary material mixture is a non-aqueous system, and a solution prepared from the mixture of the two or three auxiliary materials can be absorbed by the nasal meatus olfactory mucosa after being administrated through the nasal region mucosa, can be quickly conducted to the brain olfactory bulb region along olfactory nerves and cerebrospinal fluid, and can be used for treating the brain olfactory bulb. The problems that the peripheral side effect is high due to poor brain targeting of the medicine, the medicine takes effect slowly and the like are solved.

Provided in the present disclosure are a solid electrolyte, a preparation method therefor and a secondary battery. The solid electrolyte comprises an oxide solid electrolyte and a shell layer coating the surface of the oxide solid electrolyte, wherein the shell layer comprises a monomer polymer and an ionic liquid. The monomer polymer is obtained by copolymerizing a first polymeric monomer and a second polymeric monomer, wherein the first polymeric monomer comprises one or more of ethylene glycol monomethyl ether acrylic acid, ethylene glycol monomethyl ether methacrylate, ethylene glycol monoethyl ether methacrylate and ethylene glycol monopropyl ether methacrylate; and the second polymeric monomer comprises a fluoroacrylate. F doping is firstly selected to modify LATP in the present disclosure, thereby significantly improving the ionic conductivity of the LATP, and widening the electrochemical window thereof, which is beneficial to improving the hydrophobicity thereof. The inner structure selected in the present disclosure is an LATP material doped with F, which can form better attraction to a C-containing group in the coating layer and cations of the ionic liquid, thereby improving the coating effect of the outer layer.

The invention relates to the technical field of organic functional material synthesis and mycotoxin removal, in particular to a magnetic covalent organic framework for adsorbing zearalenone and a preparation method and application thereof.The magnetic covalent organic framework is Fe3O4 (at) COF-VPBA and is prepared from 1, 3, 5-tris (4-aminophenyl) benzene, 2, 5-dimethoxy terephthalaldehyde, 4-alkenyl phenylboronic acid, boron trifluoride diethyl etherate, 2, 3-dichloro-5, 5-di (4-aminophenyl) benzene, 2, 5-dimethoxy terephthalaldehyde, 2, 5-dimethoxy terephthalaldehyde, 2, 5-dimethoxy terephthalaldehyde, 2, 5-dimethoxy terephthalaldehyde, 2, 5-dimethoxy terephthalaldehyde, 2, 5-dimethoxy terephthalaldehyde, 2 The catalyst is prepared from 2, 6-dicyano-1, 4-benzoquinone and nano ferroferric oxide through a four-component one-pot in-situ Povarov reaction. According to the method, the process is simplified, the defects of a fractional step method are avoided, due to specific covalent binding of boric acid groups and ZEN catechol hydroxyl groups, the adsorption capacity and the adsorption rate are remarkably superior to those of traditional and unfunctionalized adsorption materials, the adsorption rate still exceeds 90% after acetonitrile is eluted and regenerated and is repeatedly used for more than 5 times, and the comprehensive requirements of high selectivity, high adsorption capacity, easiness in separation and recyclability are met.

The invention discloses a thin-layer chromatography identification method for cinnamon and ginger in vitality-preserving granules, and belongs to the technical field of pharmaceutical analysis. Aiming at the problems of step-by-step detection, serious cinnamic acid tailing and dependence on toxic solvents in the existing method, the method comprises the following steps: dissolving vitality-preserving particles in water, carrying out ultrasonic treatment, extracting filtrate by using absolute ether, merging extract liquor, evaporating to dryness, and dissolving by adding ethyl acetate to obtain a test solution; preparing a cinnamon reference medicinal material solution and a cinnamic acid and 6-gingerol reference substance solution; a silica gel GF254 thin-layer plate is adopted, petroleum ether-normal hexane-ethyl formate-formic acid is used as a developing solvent for developing, and inspection is conducted under the ultraviolet light of 254 nm and the ultraviolet light of 365 nm respectively. Cinnamon and ginger can be synchronously identified, spots are clear and free of trailing, no toxic solvent exists, durability is high, cost is low, and an accurate and reliable basis can be provided for quality control of the vitality-preserving granules.

The present application belongs to the technical field of cleaning products, and particularly relates to a high-temperature oil stain removing stove cleaner as well as a preparation method and application thereof. The high-temperature oil stain removing stove cleaner provided by the present application comprises the following components and mass fractions: 11-33 parts of an alkaline additive, 1-2 parts of hydroxyethylidene diphosphonic acid, 3-6 parts of a non-ionic surfactant, 4-8 parts of a solvent, 1-3 parts of a solubilizer, 1-3 parts of sodium xylene sulfonate, and 45-79 parts of water; the solvent comprises ethylene glycol monobutyl ether and diethylene glycol ethyl ether. The high-temperature oil stain removing stove cleaner provided by the present application has the advantages of simple cleaning method, high-temperature oil removing effect, good stain removing and oil scale removing effect on commercial kitchen utensils, high safety, no corrosion to metal, simple raw material composition, and no need to add a defoaming agent.

The application discloses an electronic skin-oriented conductive silver paste and a preparation method and application thereof, and relates to the technical field of flexible printed electronic materials.The raw materials of the electronic skin-oriented conductive silver paste include flaky silver powder, silver nanoparticles, thermoplastic polyurethane elastomer, acrylic elastomer, PEDOT:PSS microgel dispersion, (3-glycidylpropoxy)trimethoxysilane, polydiallyldimethylammonium chloride, hexanedial modified dopamine copolymer, (3-aminopropyl)triethoxysilane, methacryloyloxypropyltrimethoxysilane, cellulose acetate, modified polyurea thixotropic agent, hydrogenated castor oil, ethylene glycol ether acetate, dibasic acid ester, leveling agent and water.The electronic skin-oriented conductive silver paste has the advantages of good electrical performance, good mechanical-electrical stability, good anti-electromigration and sweat corrosion resistance, and can still maintain dendrite-free and low drift under long-term coupling of sweat and bias, and is suitable for electronic skin.

The invention relates to a continuous production method of ultra-pure 2, 3, 4, 4 '-tetrahydroxybenzophenone, which comprises the following steps: completely dissolving p-hydroxybenzoic acid in high-boiling range petroleum ether, and completely dissolving pyrogallic acid in the high-boiling range petroleum ether; the preparation method comprises the following steps: adding a p-hydroxybenzoic acid solution and a pyrogallic acid solution into an ultra-pure continuous reactor group, adding boron trifluoride diethyl etherate into the ultra-pure continuous reactor group at a flowing speed, reacting at 110-140 DEG C, adding the obtained reaction solution into the next ultra-pure continuous reactor group, stirring in ice water, filtering, washing and recrystallizing to obtain the 2, 3, 4, 5-tetramethyl-3, 5-dihydroxybenzoic acid. According to the present invention, the reaction time is substantially shortened, the conversion rate is 70-80%, the purity of the obtained electronic product is more than or equal to 99.2%, the content of the metal ions such as sodium, aluminum, copper, iron, calcium, zinc and boron is less than or equal to 60 ppb, the reaction materials, the reaction temperature and the reaction rate are controllable, the reaction is sufficient, the yield of the obtained target product is stable, and the method can be used for continuous production.

The invention discloses a ruthenium metal complex and a preparation method and application thereof, and belongs to the technical field of organic metal synthesis. The preparation method of the ruthenium metal complex specifically comprises the following steps: (1) under anhydrous and anaerobic conditions, adding ethylene glycol monoethyl ether and RuCl3.H2O into a reaction flask, introducing CO, heating, and reacting; (2) continuously heating, reacting and cooling; and (3) adding 3-chloro-2-methylpropan-1-ene, uniformly mixing, heating, stirring, cooling, adding a potassium tert-butoxide tetrahydrofuran solution, heating until boiling, stirring again, stopping heating, reacting, filtering, cleaning a filter cake with tetrahydrofuran, removing the solvent from the filtrate to obtain a reddish brown oily liquid, and condensing to obtain a Ru (tmm) (CO) 3 product, namely the ruthenium metal complex. The ruthenium metal complex prepared by the method has the advantages of high yield (62.8%), high purity (99.6%), low synthesis cost and simple synthesis steps.

The invention relates to the technical field of chemical reaction equipment, and discloses a reaction device and method for synthesizing free radicals from chloromethyl ethyl ether, the reaction device comprises a support, the inner wall of the support is rotatably connected with a shell, the top of the shell is connected with a first feeding port in a penetrating mode, and when a driving rod rotates, the driving rod drives a second gear ring and a first circular ring to rotate through a gear; due to the fact that the diameter of a first gear ring and the diameter of a second gear ring are different, the rotating speed difference exists between a first circular ring and a driving rod, metal particles enter the inner wall of the driving rod through a second feeding port, and the rotating speed difference exists between the driving rod and the first circular ring, it can be regarded that an auger rotates on the inner wall of the driving rod, and the rotating auger drives the metal particles to flow upwards; flowing metal particles flow out from the discharging port, so that the metal particles precipitated at the bottom of the reaction kettle can flow from bottom to top, and the situation that ethanol is differentiated from part of solution due to the fact that the metal particles at the bottom are heated too high is effectively prevented.

The application discloses a kind of polymer oil displacement agent for carbonate fractured-vug type reservoir and preparation method thereof, step 1, with acetone and ethanol mixed solution as solvent, N, N-dimethylpropylene diamine, diethyl ether and perfluorinated nonanoic acid are added into acetone-ethanol mixed solution, after complete reaction, chloropropene is added, continue to react, after reaction is finished, solvent is removed by evaporation, to obtain fluorocarbon cation hydrophobic monomer CF-1;Step 2, white oil, emulsifier Span80 and Tween80 with mass ratio of 35-45:1-3:1-2 are mixed uniformly to obtain oil phase;AM, sodium p-styrenesulfonate and fluorocarbon cation hydrophobic monomer CF-1 are dissolved in deionized water, sodium bisulfite is added, and stirred uniformly to obtain aqueous solution;The aqueous solution is added to the oil phase to obtain a uniform emulsion, ammonium persulfate is added, and the polymer oil displacement agent is obtained by reaction. It has higher temperature resistance and salt resistance, and greatly reduces the adsorption of carbonate reservoir on the oil displacement agent.

The invention relates to the technical field of batteries, and discloses an electrolyte and application thereof, and a lithium carbon fluoride battery. The electrolyte comprises a lithium salt and an organic solvent; wherein the lithium salt is lithium bis (fluorosulfonyl) imide; the organic solvent is selected from one of ethylene glycol dimethyl ether, diethylene glycol dimethyl ether, triethylene glycol dimethyl ether, tetraethylene glycol dimethyl ether, ethylene glycol diethyl ether, ethylene carbonate, propylene carbonate, dimethyl carbonate, ethyl methyl carbonate, dimethylformamide, dimethylacetamide and dimethyl sulfoxide. The electrolyte can be applied to preparation of a lithium primary battery. The invention also relates to a lithium carbon fluoride battery comprising the electrolyte. The electrolyte system provides an optimized solution for the preparation of the high-energy-density lithium carbon fluoride battery, has a wide application prospect, can remarkably improve the performance of the battery, reduces the production cost, and promotes the further development of the lithium carbon fluoride battery technology.

One embodiment of the present invention provides a method of producing a fibrous non-demineralized bone graft material, the method comprising: a step of removing soft tissue, blood, and bone marrow from bone; a dehydration step of immersing, in an aqueous ethanol solution, the bone from which the soft tissue, blood, and bone marrow have been removed, and stirring same; a primary defatting step of immersing and stirring the dehydrated bone in diethyl ether; a step of crushing the bone subjected to the primary defatting into fibrously processed bone; a step of screening the fibrously processed bone; a hydration step of immersing and stirring the screened fibrously processed bone in ethanol; a secondary defatting step of immersing and stirring the hydrated fibrously processed bone in hydrogen peroxide; a washing step of washing the fibrously processed bone subjected to the secondary defatting; and a freeze-drying step.

To provide a novel tetracycline derivative having reduced antimicrobial activity for use in treating disorders of the central nervous system.SOLUTION: Provided are novel molecules comprising a modified tetracycline molecule including Deamino Diacetyl Minocycline, Methyl Ether Minocycline, Ethyl Ether Minocycline, Propyl Ether Minocycline, Butyl Ether Minocycline, Butyl Ether Monoacetyl Minocycline, Butyl Ether Diacetyl Minocycline, Butyl Ether Triacetyl Minocycline, or Butyl Ether Tetra Acetyl Minocycline, pharmaceutically acceptable salts, pro-drugs, biologically active metabolites, and tautomers thereof, and methods for using the same to treat Alcohol Use Disorder (AUD), Substance Use Disorder (SUD), tobacco use, pain, or proinflammatory disorders.SELECTED DRAWING: None

The application discloses a ginseng polysaccharide, a preparation method and application, and the ginseng polysaccharide is ginseng polysaccharide GP60, which is composed of glucose, galactose and arabinose, and the molar ratio of each monosaccharide is glucose: galactose: arabinose = 77.1: 16.8: 6.1; a new preparation method is adopted; after soaking and twice decocting, different proportions of 95% ethanol are added into the filtrate in batches; the obtained precipitate is added with water to prepare a solution with a relative density of 1.1 g / ml; a certain amount of the solution is taken, a certain proportion of chloroform and n-butanol is added, and a polysaccharide aqueous solution is prepared; the polysaccharide aqueous solution is added with 95% ethanol until the alcohol content reaches 60%; the solution is statically placed for 12 hours; centrifugal separation is carried out; the precipitate is collected; the collected precipitate is sequentially washed with 95% ethanol, anhydrous ethanol, isopropyl alcohol and ether; the solvent is volatilized; and the ginseng polysaccharide GP60 is obtained. The ginseng polysaccharide GP60 is non-toxic, has the effect of preventing light aging, and can be widely applied in the fields of food or health food, anti-light aging skin care products, washing and caring products and anti-light aging medicines.

The application relates to a component detection method of a cosmetic liquid and a permeability detection method of the cosmetic liquid, and the component detection method comprises the following steps: adding a protein precipitant to purify the cosmetic liquid; performing liquid chromatography-tandem mass spectrometry on the purified cosmetic liquid to obtain chromatographic peak response values of nicotinamide, ascorbic acid and VC ethyl ether; wherein, the positive ion and the negative ion are alternately ionized in the mass spectrometry, and multiple reaction monitoring is performed on the nicotinamide, the ascorbic acid and the VC ethyl ether; and the concentrations of the nicotinamide, the ascorbic acid and the VC ethyl ether in the cosmetic liquid are obtained according to the chromatographic peak response values. The method improves the detection precision of low-concentration and multi-target component.

The invention discloses a method for detecting sweet-scented osmanthus aroma components in sweet-scented osmanthus wine, which comprises the following steps: diluting a wine sample, adding salt until the wine sample is saturated, and then carrying out liquid-liquid micro-extraction by using a mixed solvent of absolute ether and ethyl acetate in a specific ratio, the volume fraction of the ethyl acetate being 3-5%; after oscillation, ultrasonic-assisted extraction and centrifugal separation, an organic phase is taken for dehydration, a gas chromatograph-mass spectrometer is used for analysis, and an internal standard method is adopted for quantification. By optimizing the polarity of the solvent, various aroma components (such as leaf alcohol, linalool oxide, linalool, ionone, tea aroma spirane and the like) from strong polarity to weak polarity can be effectively covered, and balanced and efficient extraction under a single extraction step is realized. The method is easy and convenient to operate, high in recovery rate, good in reproducibility and suitable for quality evaluation and production process control of the osmanthus fragrans wine.

The invention relates to a sodium-ion battery modification method of a high-performance electrolyte additive, and belongs to the field of electrochemical energy storage of a sodium-ion battery composite positive electrode material. According to the method, a proper amount of 2, 2, 2-trifluoroethyl ether is introduced in the liquid injection process of a soft package sodium-ion battery to serve as the electrolyte additive, the solvation energy of sodium ions in an electrolyte can be reduced, and the performance of the sodium-ion battery is improved. The ion transmission capability and the conductivity of sodium ions in the electrolyte are improved, the sodium ion intercalation and deintercalation kinetics of the battery in the charge and discharge process is improved, and the charge and discharge electrochemical properties such as high first effect, high capacity, long cycle and high rate are realized. Besides, 2, 2, 2-trifluoroethyl ether serving as an electrolyte additive can also play a role in protecting positive and negative electrode material structures of the sodium-ion battery in the charging and discharging process, and damage and structural collapse of the materials in the circulating process are reduced, so that the circulating stability and safety performance of the battery are improved.

The application discloses an end hexaazido nitrate polyether adhesive and a synthesis method thereof. The method first takes triazido neopentyl alcohol and glycidyl ether nitrate as raw materials, boron trifluoride-ether complex as a catalyst, and obtains triazido neopentyl polyglycidyl ether nitrate alcohol through cation ring-opening polymerization reaction; then takes triazido neopentyl polyglycidyl ether nitrate alcohol and hexamethylene diisocyanate as raw materials, dibutyl tin dilaurylate as a catalyst, and obtains end hexaazido polyglycidyl ether nitrate through addition reaction, namely the end hexaazido nitrate polyether adhesive. The application is mainly used for solid propellants, is used for synthesizing polytriazole elastomers, improves the content and crosslinking density of hard segments, promotes microphase separation of the elastomers, and thus improves mechanical properties.

A method of hydrogenation includes contacting a catalyst, including rhodium nanoparticles in an amount of 0.9 percent by weight (wt. %) to 1.1 wt. % based on the total weight of the catalyst supported on alumina, with furfural in the presence of ethanol to form a reaction mixture. The method further includes heating the reaction mixture at a pressure, at a temperature, and for a time, in a hydrogen gas atmosphere to form a hydrogenated product including furfuryl ethyl ether. At least 99 wt. % of the furfural is reacted to form the furfuryl ethyl ether and the furfuryl ethyl ether is formed with at least a 99 wt. % selectivity.

The application discloses a water-based zinc ion battery electrolyte, a preparation method and application thereof. The water-based zinc ion battery electrolyte contains a zinc salt, ethylene glycol ether and water. The zinc salt is selected from at least one of ZnSO4, ZnCl2 and Zn(OTf)2. In the water-based zinc ion battery electrolyte, the mass content of the ethylene glycol ether is 1-20 wt%. The concentration of the zinc salt is 3M.

The present application relates to the technical field of water-based gloss oil, and specifically discloses a high-adhesion water-based polyester gloss oil coating and a preparation method thereof. The high-adhesion water-based polyester gloss oil coating comprises polyurethane resin, polyester resin, defoaming agent, leveling agent, surfactant and wetting dispersant, the weight ratio of the polyurethane resin and the polyester resin is 30-45:12-20, and the solvent comprises ethylene glycol butyl ether and / or ethylene glycol ether. The main agent in the high-adhesion water-based polyester gloss oil coating of the present application can form a film structure with stable structure and good compactness through cross-linking reaction under the action of the auxiliary agent, and the coating has higher adhesion, wear resistance, yellowing resistance and gloss after coating, and is more suitable for industrial expansion production.

The invention relates to the technical field of material surface treatment, in particular to a heat transfer printing ceramic coating and a preparation method and application thereof. The raw materials comprise the following components: inorganic silica sol, hydroxy acrylic resin, nano aluminum oxide slurry, nano zirconium oxide slurry, a silane coupling agent (KH-550), a flatting agent (BYK-346), a defoaming agent (BYK-066N), an ultraviolet light absorber (UV-327) and a solvent (ethylene glycol monoethyl ether acetate); comprising the following steps: step 1, premixing; 2, dispersing the nano slurry at a high speed; 3, carrying out inorganic and organic hybridization reaction; 4, paint mixing and filtering; step 5, coating treatment; the coating solves the technical problems that a traditional heat transfer printing coating is low in hardness, not resistant to abrasion, easy to fade, not resistant to acid and alkali and the like, and the nano ceramic coating which is extremely high in hardness, excellent in abrasion resistance, excellent in color retention and resistant to chemical corrosion is formed. And the paint can be widely applied to decoration protection of high-end building materials, home furnishing and electric appliance products with high surface performance requirements.

The utility model discloses an electric guard compact type intelligent fire extinguishing device, and relates to the technical field of fire extinguishing devices. The compact intelligent fire extinguishing device for the electric guard is L-shaped on the whole and comprises a fire extinguisher main body with a cylindrical structure and a steering spray head which is mounted at the end part of the fire extinguisher main body and forms an angle of 90 degrees with the fire extinguisher main body; a perfluorohexanone fire extinguishing agent and nitrogen are stored in the fire extinguisher main body; a diffuser is installed on the steering nozzle, and an ether liquid glass tube is adopted as a channel switch between the diffuser and the steering nozzle. The compact intelligent fire extinguishing device for electric guards is particularly suitable for fire treatment in narrow and small spaces, can automatically sense high temperature or open fire, can be quickly started, and can extinguish fire under the condition of minimum manual intervention; according to the fire extinguishing device, the safety of electrical equipment is improved, economic losses caused by fire disasters are reduced, and negative effects on the environment are reduced due to the fact that the environment-friendly fire extinguishing agent is used.

The application discloses a pyrrole polymer electrolyte film in an energy storage lithium battery and a preparation method and application thereof, and belongs to the polymer electrolyte field. The method comprises the following steps: reacting 1-methyl pyrrolidine and bromine n-butane to prepare 1-methyl-1-butyl pyrrolidine bromide; preparing 1-methyl-1-butyl pyrrolidine difluoromethane sulfonimide salt ionic liquid by mixing the 1-methyl-1-butyl pyrrolidine bromide and lithium difluoromethane sulfonimide; mixing 1-methyl-1-butyl pyrrolidine difluoromethane sulfonimide salt ionic liquid, polyethylene glycol methyl ether methacrylate, acrylonitrile, lithium bistrifluoromethanesulfonimide, divinylbenzene and benzoin ethyl ether uniformly, coating and curing to obtain a pyrrole ionic liquid polymer electrolyte film. The application combines the molecular configuration of the pyrrolidine-based ionic liquid and the topological structure of the polymer network, realizes triple optimization of ion transmission-mechanical strength-interface stability.

The invention discloses a method for producing recombinant I-type mussel mucin rich in dopa, and belongs to the technical field of genetic engineering. According to the invention, Ala-Lys-Pro-Ser-Tyr-Pro-Pro-Thr-Tyr-Lys decapeptide of a natural type I mussel mucin sequence is taken as a repetitive unit, a gene expression vector for tandem expression of peptide fragments with different repetitive numbers is constructed, and pichia pastoris host bacteria are transformed, so that type I mussel mucin precursors with different molecular weights are obtained; in vitro, a precursor is subjected to dopa modification by high-activity tyrosinase obtained through screening in a mixed system containing ascorbic acid ethyl ether, copper sulfate and the like, and the recombinant I-type mussel mucin rich in dopa groups is obtained after purification. The recombinant I-type mussel mucin rich in dopa obtained by the invention has the advantages of high purity and high dopa modification rate, and has wide application prospects in the fields of biomedicine, surface chemistry and the like.

This application relates to the field of waterborne cathodic electrophoretic coating technology, specifically disclosing a bisphenol A epoxy-polyetheramine composite matte electrophoretic emulsion and its preparation method. The bisphenol A epoxy-polyetheramine composite matte electrophoretic emulsion comprises the following raw materials in parts by weight: 30-40 parts E-51 epoxy resin, 8-10 parts bisphenol A, 9-11 parts bisphenol A polyoxyethylene ether, 0.08-0.12 parts benzylamine, 2.5-3.5 parts methylethanolamine, 0.8-1.2 parts diethylene glycolamine, and 2.5-3.5 parts ketimine. This application uses E-51 epoxy resin, bisphenol A, and bisphenol A polyoxyethylene ether as the matrix skeleton, and obtains an epoxy equivalent prepolymer after chain extension catalyzed by benzylamine. At the same time, toluene diisocyanate is reacted with diethylene glycol butyl ether, diethylene glycol ethyl ether, and trimethylolpropane polyoxyethylene ether to prepare a blocked crosslinking agent, thereby achieving a uniform internal matting effect without the addition of external matting powder.

A process of converting an ethanol feed stream to ethylene comprising sending portions of said ethanol feed stream to two reactors in parallel and then sending the combined product to a third reactor that is operated at a higher temperature to prevent the formation of ethers such as diethyl ether.