241 results about "Alkoxide" patented technology

The invention relates to a novel composite bipolar membrane for preparing low-carbon alcohol alkali metal salt and an electrodialysis process of the novel composite bipolar membrane, and belongs to the technical field of membrane separation and electrochemical synthesis. The composite bipolar membrane comprises a cation exchange layer, a middle catalyst layer and an anion exchange layer which are sequentially laminated and compounded, the process comprises the following steps: introducing a salt solution containing alkali metal ions into an anode chamber of a bipolar membrane electrodialysis system, and introducing a low-carbon alcohol solution into a cathode chamber; applying a direct-current electric field to the two sides of the composite bipolar membrane, so that the low-carbon alcohol is dissociated at the membrane interface to generate alkoxy ions and hydrogen ions; the alkoxy ions migrate to an anode chamber to be combined with the alkali metal ions to generate low-carbon alcohol alkali metal salt; the membrane material is high in adaptability, the membrane structure is good in stability, technological parameters are mature, and the system integration degree is high.

The invention belongs to the technical field of chemical engineering, and particularly relates to an aluminum alkoxide salt and a preparation method thereof. According to the method, argon non-thermal plasma is adopted for bombarding the surface of the aluminum foil, an oxidation film on the surface of the aluminum foil is stripped, active aluminum free radicals are formed, the reaction energy barrier of the aluminum alkoxide salt is reduced, the aluminum alkoxide salt can be synthesized under the catalyst-free condition, and green and efficient synthesis of the aluminum alkoxide salt is achieved; a thiosemicarbazide-carboxylic acid bidentate ligand is adopted for complexing impurity iron in alkoxide aluminum salt, sulfur and nitrogen double coordination sites in a thiosemicarbazide unit are matched with oxygen coordination sites in a carboxylic acid group, higher complexing capacity is formed for the impurity iron, and the stability of the complex is improved; the crystallization is regulated and controlled through the pH response characteristic of the carboxylic acid group, so that the impurity iron in the aluminum alkoxide salt is efficiently removed.

A separator and a method for manufacturing thereof are disclosed. The separator comprises an enhanced porous polyolefin substrate and an inorganic layer, wherein the enhanced porous polyolefin substrate is obtained by pre-strengthening a porous polyolefin substrate, and the inorganic layer comprises a plurality of inorganic particles and a binder and coated on at least one surface of the enhanced porous polyolefin substrate, and the pre-strengthening treatment comprises sequentially applying a titanium alkoxide solution and an alcohol solution. The separator of the present invention has improved tensile strength and good compression resistance.

Organotin compositions suitable for radiation based patterning have ligands providing fluorinated groups and unsaturated carbon-carbon bonds, such as C═C bonds. The fluorinated groups and unsaturated carbon-carbon bonds may or may not be located on the same ligand. Blends of precursors with different ligands provide added flexibility with respect to precursor design. Fluorinated organometallic compounds can be represented by the formula RUFSn(OR′)3, wherein RUF is an organo group with 1 to 31 carbon atoms with at least one C═C bond and at least one fluorine atom bonded to a carbon, with the organo group forming a C—Sn bond, wherein R′ is an organo group with 1 to 10 carbon atoms. Precursors are suitable for solution based deposition or vapor based deposition.

The utility model discloses a continuous production device for hydrolyzing and drying aluminum alkoxide, which belongs to the technical field of chemical equipment and comprises a primary hydrolyzing and drying unit and a secondary hydrolyzing and drying unit. The primary hydrolysis drying unit comprises a primary hydrolysis reaction kettle, a primary belt type vacuum dryer, an anhydrous alcohol condenser and an anhydrous alcohol recovery tank; the secondary hydrolysis drying unit comprises a secondary hydrolysis reaction kettle, a secondary belt type vacuum dryer, a water-containing alcohol condenser and a water-containing alcohol recovery tank; materials discharged from the discharging end of the primary belt type vacuum dryer are conveyed to the secondary hydrolysis reaction kettle, and the bottom of the water-containing alcohol recovery tank is connected with a feeding port of the primary hydrolysis reaction kettle. Anhydrous alcohol obtained from the primary hydrolysis reaction kettle is recycled and then used as a raw material for synthesizing aluminum alkoxide, and water-containing alcohol obtained from the secondary hydrolysis reaction kettle is used as a raw material for hydrolysis reaction, so that recycling of alcohol is realized; and a belt type vacuum dryer is adopted to continuously dry mixed solutions obtained by two times of hydrolysis respectively, so that continuous hydrolysis and drying production is realized.

The invention discloses a preparation method and application of ultrahigh-temperature-resistant tantalum carbide ceramic aerogel, and belongs to the field of ultrahigh-temperature ceramic aerogel preparation. The preparation method of the ultrahigh-temperature-resistant tantalum carbide ceramic aerogel comprises the following steps: mixing a complexing agent and tantalum alkoxide in a polyol solvent for reaction, then adding organic acid for catalytic polymerization, then adding phenolic resin and a gel catalyst to obtain a tantalum carbide precursor solution, and carrying out sol-gel reaction to obtain tantalum carbide precursor wet gel; performing drying treatment on the tantalum carbide precursor wet gel to obtain tantalum carbide precursor aerogel, and performing pyrolysis to obtain the tantalum carbide ceramic aerogel. The tantalum alkoxide is modified by using the complexing agent, the polyhydric alcohol and the organic acid, the precursor solution in which the raw materials can stably coexist at room temperature is obtained, an oxide ceramic gel network does not need to be synthesized in the preparation process, normal-pressure drying can be performed, and the obtained tantalum carbide ceramic aerogel has the characteristics of high purity and low residual carbon content.

The invention belongs to the technical field of pharmaceutical chemicals, and particularly relates to a synthetic method of ethylhexylglycerin. The preparation method comprises the following steps: carrying out Williamson reaction on 2-ethylhexyl alkoxide and 4-(chloromethyl)-2, 2-dimethyl-1, 3-dioxolane to obtain 4-[((2-ethylhexyl) oxy) methyl]-2, 2-dimethyl-1, 3-dioxolane, adding an aqueous solution of acid into a system after the reaction is completed, and carrying out ketal removal reaction to obtain ethylhexyl glycerol. According to the ethylhexylglycerin prepared by the synthesis method provided by the invention, the yield is up to 95% or above, and the purity is up to 99.9% or above.

A process can be used for electrochemical preparation of an alkali metal alkoxide solution. The process is performed in an electrolysis cell having three chambers, where the middle chamber is separated from the cathode chamber by a solid-state electrolyte permeable to cations, for example NaSICON, and from the anode chamber by a diffusion barrier, for example a membrane selective for cations or anions. The process solves a problem where a concentration gradient forms in the middle chamber of the electrolysis cell during the electrolysis, which leads to locally lowered pH values and damage to the solid-state electrolyte used. This is prevented where a gas is introduced into the middle chamber during the electrolysis, which results in better mixing of the electrolyte solution in the middle chamber and prevents the formation of a concentration gradient.

The invention provides a preparation method of bis-[3-(triethoxysilyl) propyl]-disulfide. The preparation method comprises the following steps: S1, under the protection of nitrogen, dropwise adding chloropropene and trichlorosilane into a non-polar solvent, a first catalyst and tripropylamine, reacting at room temperature, taking filtrate, dropwise adding the filtrate into alcohol in a micro-reflux state, reacting, adding a sodium alkoxide / alcohol solution for neutralizing, filtering, and distilling to obtain allyltriethoxysilane; and S2, under ultraviolet light, mixing allyltriethoxysilane, mercaptopropyltriethoxysilane and benzoin dimethyl ether, reacting at room temperature for 2-3 hours, adding sulfur and a second catalyst, carrying out heating reaction, removing low boiling points, cooling, and filtering. According to the preparation method provided by the invention, bis-[3-(triethoxysilyl) propyl]-disulfide is successfully and effectively synthesized, a phase transfer catalyst does not need to be introduced for catalysis, hydrolysis of silane and treatment of saline water are reduced, the yield of single-kettle synthesis is high, and the utilization rate of equipment is high.

The invention discloses a hydrogenated butadiene-acrylonitrile rubber composite material for cryogenic heat preservation and a preparation method thereof in the field of polymer composite materials, and the composite material is characterized in that zirconium-silicon composite modified hydroxyapatite and boron-nitrogen co-doped mesoporous alumina are introduced, so that the mechanical property and heat preservation effect of the material in a low-temperature environment are remarkably improved. The zirconium-silicon oxide network is constructed on the surface of hydroxyapatite by adopting a sol-gel method, and the doped mesoporous structure with the high specific surface area is obtained by adopting alkoxide as a precursor through hydrothermal treatment and calcination. When the rubber is mixed, the functional filler is dispersed at a high temperature, and then the plasticizer is added to ensure uniform distribution of the filler. The obtained composite material has excellent tensile strength, elongation at break and low heat conductivity coefficient at the liquid nitrogen temperature, and is suitable for the cryogenic thermal insulation fields of hydrogen energy storage and transportation, aerospace sealing and the like. All the raw materials are commercially available chemicals, the process is controllable, and industrial production is easy.

The present invention provides a preparation method of benzopyrone. The preparation method includes: step S1, using trifluoronitrobenzene as the first raw material, performing ortho-substitution reaction with nitromethane to obtain 1,2-difluoro-4-nitro-3-nitromethylenebenzene, and performing para-substitution reaction with alkoxide to obtain a first intermediate; step S2, subjecting the first intermediate to a Nef reaction, converting the nitromethyl group to a carboxyl group to obtain a second intermediate; step S3, subjecting the second intermediate to a reduction reaction, an oxidation reaction, and a denitrogenation rearrangement reaction to convert the nitro group to an aldehyde hydrazine to obtain an aldehyde hydrazine intermediate; step S4, under the action of a catalyst, subjecting the aldehyde hydrazine intermediate to a nucleophilic addition reaction with the second raw material to generate a secondary alcohol intermediate, and subjecting the secondary alcohol intermediate to a ring-closing reaction to obtain a target product. The above-mentioned method for preparing benzopyrone has a wide range of raw material sources, relatively mild reaction conditions, and a high overall reaction yield.

A process for the production of a C6-18 alkyl ester of 4-aminobenzoic acid of formula (I), wherein the process comprises the step of reacting the 4-aminobenzoic acid of formula (II) with an hydroxy compound of formula (III) in the presence of a catalyst to generate a C6-18 alkyl ester of 4-aminobenzoic acid of formula (I) wherein R is a C6-18 alkyl group; and wherein the catalyst is a titanium catalyst, preferably a titanium alkoxide catalyst.

The invention relates to the field of anticorrosive coatings, in particular to a high-molecular heavy-duty anticorrosive material for improving the quality of strip steel of a hot rolling mill and a preparation process thereof. A high-molecular heavy anti-corrosion material for improving the quality of strip steel of a hot rolling mill comprises the following raw materials in parts by mass: 55-70 parts of aliphatic dicarboxylic acid alkoxide, 15-30 parts of modified polysiloxane, 2-4 parts of a pH regulator, 3-5 parts of a corrosion inhibitor, 1-3 parts of a preservative, 1-5 parts of a plasticizer, 2.5-5 parts of a wetting dispersant, 5-10 parts of filling particles and 30-50 parts of deionized water. The high-temperature-resistant anticorrosive paint prepared by the invention not only can be used as a special heavy-duty anticorrosive paint for a hot rolling unit in the iron and steel industry, but also has excellent high-temperature resistance, so that the durability of the high-temperature-resistant anticorrosive paint in a high-temperature and high-humidity environment is improved, and the high-temperature-resistant anticorrosive paint also shows excellent performance in the aspects of aging resistance, oxidation resistance, corrosion resistance and the like; therefore, the comprehensive performance requirements of related equipment on the high-temperature-resistant anticorrosive paint in the existing steel hot rolling production process are met, and the high-temperature-resistant anticorrosive paint has a very excellent application prospect.

A system and method for chemically destroying, degrading and incinerating a fluorocarbon or fluorinated material, such as perfluoroalkyl and polyfluoroalkyl substances (PFAS), with reduced emissions of gaseous PFC is provided. The method includes mixing the fluorinated material with an aqueous alkoxide base in a batch reactor to form a suspension. The PFAS can be provided by AFFF. The reaction mixture is heated to a temperature ranging from about 25ºC to about 400ºC for about 0.5 hours to about 240 hours to defluorinated fluorocarbons in the PFAS and produce a defluorinated waste product. More specifically, the method converts organic fluorine present in the PFAS to inorganic fluoride. Thus, the defluorinated waste product can be incinerated with reduced emissions of harmful gaseous PFCs.

This invention relates to a process for preparing an intermediate of aminoimidazole carboxylate, a process for synthesizing aminoimidazole carboxylate and an HPLC method for determining purity. The process of preparing the intermediate of aminoimidazole carboxylate comprises subjecting a compound of formula I-2 and a formate as the reactants to a first-step reaction in a benzene solvent and at a temperature of −5° C.−5° C., with the addition of a solution of sodium alkoxide in such a way that the temperature of the reaction solution is not higher than 5° C., to obtain the intermediate of aminoimidazole carboxylate or a mixture comprising a compound of formula I-3, i.e., the intermediate of aminoimidazole carboxylate. By using a sodium alkoxide reagent, as a comparatively safe alternative to NaH and potassium tert-butoxide which are prone to cause fire hazards or explosions and are not suitable for use in large-scale production, the process of the present application can ensure smooth progression of the reaction to the product and effectively improve the overall safety of the reaction without noticeably impairing the reaction efficiency.

This invention discloses a veterinary aluminum hydroxide adjuvant for foot-and-mouth disease (FMD) vaccines and its preparation method via aluminum alkoxide hydrolysis. The adjuvant is a boehmite phase, and through innovative processing, the crystallinity and morphology are synergistically controlled, achieving a relative crystallinity of 10%-25%. The primary particles are rod-shaped or needle-shaped, with an average aspect ratio of 4:1 to 8:1. The preparation method includes: dissolving an aluminum alkoxide compound, then subjecting it to a controlled hydrolysis reaction at 50-80℃ and pH 4.5-6.5 under normal pressure for 36 hours, followed by aging at 425℃ for 2472 hours. The product is obtained after solid-liquid separation, washing, and drying. The obtained adjuvant exhibits an adsorption rate of over 96% for FMD virus inactivated antigen within 1 hour, and a cumulative antigen dissociation rate of less than 5% after 7 days at 37℃. In vitro stimulation of macrophages to secrete IL-1β and TNF-α levels is more than 1.7 times that of commercially available aluminum hydroxide adjuvants, significantly superior to traditional aluminum hydroxide adjuvants, providing a new material for the preparation of highly effective FMD vaccines.

The film includes a substrate and a coating deposited on the substrate. The coating includes a plurality of bilayers, each including two layers of different materials. Each of the two layers of different materials may comprise an oxide, a metal oxide, an alkoxide, an MLD method metal inorganic-organic hybrid, or an oxynitride. The thickness of each of the two layers of different materials may be from about 3 nanometers to about 30 nanometers. The thickness of the coating may be from about 20 nanometers to about 100 nanometers. The film with its nanoscale coating may be used in food packaging and other applications.

This invention relates to an electrolyte for lithium-ion batteries or lithium metal batteries, a method for preparing the electrolyte, and a lithium battery. The electrolyte comprises a lithium salt, an organic solvent, and functional additives, wherein the functional additives include aluminum alkoxide compounds. A battery containing the additives is also provided. Based on the discovery that ethylene carbonate (EC) degrades battery thermal safety under high-temperature thermal abuse conditions, aluminum isopropoxide is innovatively introduced as a functional additive. This additive is stable at room temperature, but under high-temperature thermal abuse scenarios, it can act as a Lewis acid catalyst, specifically catalyzing the ring-opening polymerization reaction of EC in the electrolyte to generate polymer segments. Compared with existing technologies, the electrolyte provided by this invention effectively improves the high-temperature storage performance and thermal shock resistance of the battery without sacrificing its room-temperature electrochemical performance.

Methods for forming a vapor deposition precursor are provided. The method comprises contacting an aluminum halide compound, an alkoxy aluminum compound, and a Grignard reagent to form the vapor deposition precursor. The vapor deposition precursor comprises an dialkyl aluminum alkoxide compound. The vapor deposition precursor is formed without use of a pyrophoric compound. Related compositions, related precursors, and related methods are also provided, among other things.

The present invention relates to a process for preparing at least one alkali metal methoxide by reactive distillation in at least one reaction column. At the lower end of the reaction column(s), the respective alkali metal methoxide dissolved in methanol is withdrawn. The methanol / water mixture obtained at the top of the reaction column(s) is separated by distillation in a rectification column.The vapours obtained at the upper end of the rectification column are compressed in at least two stages and the energy of the vapours compressed in each case is advantageously transferred to bottoms and side streams of the rectification column. This allows particularly efficient use of the energy of the compressed vapours in the process according to the invention. In addition, the energy in the product stream of alkali metal methoxide which is obtained at the lower end of the reaction column(s) is advantageously transferred to the vapour streams from the rectification column, especially before these vapours are subjected to compression.The energy from the compressed vapour may additionally be used for operation of the reaction column(s) or for operation of a reaction column in which a process for transalcoholization of alkali metal alkoxides is performed.

The invention provides non-isocyanate polyurea and a preparation method thereof, water-based non-isocyanate polyurea and a preparation method thereof, and an anticorrosive coating, a waterproof coating and a fireproof coating containing the water-based non-isocyanate polyurea. The preparation method of the non-isocyanate polyurea comprises the following steps: (1) mixing alkali metal alkoxide and ionic liquid to obtain an alkali metal alkoxide / ionic liquid composite catalyst; and (2) in the presence of an alkali metal alkoxide / ionic liquid composite catalyst, polyether amine and an organic solvent are mixed, then carbon dioxide is introduced for a reaction, the non-isocyanate polyurea is obtained, and polyether amine is amino-terminated polyoxypropylene diamine or amino-terminated polyoxypropylene triamine with the number-average molecular weight ranging from 230 to 5000. According to the method, the non-isocyanate polyurea can be prepared at a high reaction rate through a simple process route, and a product obtained by taking the non-isocyanate polyurea obtained by the preparation method as a raw material has excellent application performance (including mechanical performance, water resistance, fire resistance and the like).

A liquid treatment composition for remediating and removing mercaptans from contaminated hydrocarbon liquids, the treatment composition including a hydrocarbon liquid, at least one alkoxide compound, and at least one terpene. A collective content of the at least one alkoxide compound in the liquid treatment composition is in a range of 1-20 wt % weight, a collective content of the at least one terpene in the liquid treatment composition is 5-25 vol %, a content of the hydrocarbon liquid in the treatment solution is 50-90 vol %.

The present invention relates to a safe flame-retardant electrolyte and a preparation method thereof, belonging to the technical field of lithium batteries. The electrolyte includes: 11.2 - 13.8 wt% of a lithium salt, 5.5 - 7.0 wt% of a modified phosphazene flame retardant, 2.6 - 3.2 wt% of an auxiliary additive, and the balance is a composite solvent; wherein, the modified phosphazene flame retardant uses tetrafluorobutylene glycol as a raw material, is treated with sodium hydride to synthesize a fluoride with an alkoxide structure, reacts with a hexachlorocyclotriphosphazene matrix, grafts a fluorine-containing group onto the hexachlorocyclotriphosphazene, and then the end is modified with dimethylethenylchlorosilane to introduce an organosilicon and a double bond structure, endowing the electrolyte with good flame retardancy, and at the same time, a silicon-containing protective film can be formed on the surface of the electrode material, reducing the thermal decomposition of the electrode material and the solvent erosion, so that the lithium battery exhibits excellent high-temperature stability.

The invention provides a bromo-oxime ether content detection method which is characterized by comprising the following steps: adding a bromo-oxime ether reaction solution into an anhydrous aprotic polar solvent, adding a sodium alkoxide solution for reaction, and purifying to obtain a standard sample of a bromo-oxime ether sodium alkoxide derivative; adding the bromo-oxime ether reaction solution into an anhydrous aprotic polar solvent, and adding a sodium alkoxide solution for reaction to obtain a to-be-detected sample of the bromo-oxime ether sodium alkoxide derivative; and analyzing the standard sample and the sample to be detected by adopting a high performance liquid chromatography external standard method to obtain the content of bromo-oxime ether in the bromo-oxime ether reaction liquid. The method is high in detection accuracy, good in repeatability and suitable for being applied to the scenes of laboratory research and development, factory production and the like.

The present invention discloses a synthesis method and application of a tantalum carbide precursor containing an unsaturated bond. The synthesis method uses unsaturated alcohol instead of saturated alcohol to synthesize tantalum alkoxide (i.e., an unsaturated alcohol solution in which tantalum salt is dissolved), uses tantalum alkoxide as a tantalum source, and uses allyl phenolic resin as a carbon source. The TaC precursor is synthesized by free radical copolymerization. More C=C bond crosslinking sites are introduced into the precursor, so that the tantalum source and the carbon source are mixed intramolecularly through the C=C bond addition polymerization reaction, thereby improving the crosslinking degree of the precursor. The technical problem of few crosslinking sites and failure to achieve intramolecular mixing of the tantalum source and the carbon source in the prior art is solved.

A low thermal shrinkage separator and a method for manufacturing thereof is disclosed. The method comprises providing a porous polyolefin substrate with a plurality of porous structures on surfaces and interiors thereof, and applying a prescursor solution comprising a titanium alkoxide and hexamethyldisilazane and subsequently applying an alcohol solution to form a low thermal shrinkage thin film formed on the surfaces and the sidewalls of the porous structures of the porous polyolefin substrate. The present method can enhance the low thermal shrinkage and electrolyte wettability of the separator.

The present invention relates to a silicon precursor compound in an asymmetric structure containing an alkoxide capable of preparing a silicon-containing thin film with high quality, to a method for preparing the same, and to a method for preparing a silicon-containing thin film using the silicon precursor compound in an asymmetric structure containing an alkoxide.

A separator and a method for manufacturing thereof are disclosed. The separator comprises an enhanced porous polyolefin substrate and an inorganic layer, wherein the enhanced porous polyolefin substrate is obtained by pre-strengthening a porous polyolefin substrate, and the inorganic layer comprises a plurality of inorganic particles and a binder and coated on at least one surface of the enhanced porous polyolefin substrate, and the pre-strengthening treatment comprises sequentially applying a titanium alkoxide solution and an alcohol solution. The separator of the present invention has improved tensile strength and good compression resistance.

Organotin compositions suitable for radiation-based patterning have ligands that provide a fluorinated group and an unsaturated carbon-carbon bond, such as a C=C bond. The fluorinated group and the unsaturated carbon-carbon bond may or may not be located on the same ligand. Blends of precursors with different ligands provide additional flexibility in precursor design. Fluorinated organometallic compounds are given by formula R UF It can be expressed by Sn(OR')3, where R UF R' is an organic group consisting of 1 to 31 carbon atoms, having at least one C=C bond and at least one fluorine atom bonded to carbon, and this organic group forms a C-Sn bond, while R' is an organic group consisting of 1 to 10 carbon atoms. The precursor is suitable for liquid-phase or gas-phase deposition.

The invention discloses a photosensitive nanocrystal material and a preparation method thereof, and belongs to the technical field of photoresist production processes. In order to solve the problems that an existing photoresist material is low in light absorption efficiency, insufficient in resolution ratio and complex in preparation, an Hf / Zr mixed metal alkoxide precursor is adopted, and the photoresist material is prepared through the steps of anhydrous hydrolysis, two-phase reaction, surface modification, photosensitive addition and the like. The method specifically comprises the following steps: (i) dropwise adding ultrapure water at a low temperature to react with a first ligand A to form 1.5-3nm metal oxide nanocrystalline sol; (ii) reacting alkali liquor in the two-phase system to grow crystals; (iii) carrying out surface modification on the bridged ligand B and the second ligand C; and (iv) adding a photoacid generator and a free radical photoinitiator, filtering with a filter membrane, and pre-drying to form the membrane. The material is suitable for a negative photoetching process, and the EUV absorption efficiency is gt; 85%, LWRlt; 2 nm. The method is simple to operate, and the yield is gt; the stability and the resolution ratio of the material are remarkably improved, and the material is suitable for sub-10nm semiconductor photoetching.