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62results about How to "Avoid high temperature reaction" patented technology

A kind of preparation method of graphene material

The invention discloses a preparation method of a graphene material. The preparation method comprises the following steps of: with graphite carbon as a raw material, adding potassium hypermanganate and concentrated sulfuric acid in batches in different stages to control an oxidation process of graphite; adjusting the pH value of the oxidized solution to obtain graphene oxide colloidal dispersing solutions (GOS) with different concentrations; dropwise adding the GOS on the surface of a carrier or spreading out the GOS on a non-intersolubility liquid/liquid interface and drawing into a grapheneoxide thin-film (GOF); carrying out high-speed centrifugation and drying treatment on the GOS to obtain graphene oxide solid powder (GOP); reducing the GOS by selecting an appropriate reducing agent,and centrifugally drying to obtain reduced graphene solid powder (GRP); dispersing a proper amount of GRP in an organic solvent to prepare a reduced graphene oxide colloidal dispersing solution (GRS); and dropwise adding the GRS on the surface of the carrier or spreading out on the non-intersolubility liquid/liquid interface and drawing into the reduced graphene thin-film (GRF). Various graphene materials prepared by the invention are easy to mutually transform; and the concentration of the colloidal solution and the thickness of the thin-film can be controlled in a certain range.
Owner:CENT SOUTH UNIV

Method for synthesizing allyl polyether-type high-performance water reducing agent

The invention relates to a synthetic method for an allyl polyether-type high efficiency water reducing agent, belonging to the field of water reducing agent. The synthetic method utilizes allyl polyoxyethylene ether monomer, maleic-anhydride, and a mixture with one or more of (methyl) sodium allylsulfonate, 2-acryl amide-2-methylpropanesulfonic acid, itaconic acid, acrylic acid and acrylamide for obtaining polyether-type high efficiency water reducing agent by initiating one-step polymerization through inorganic peroxides in water solution system, the final structure of the water reducing agent comprises no ester bond, carboxyl, amide, sulfonic group and other functional groups. The synthetic method for an allyl polyether-type high efficiency water reducing agent has the advantages of having applicability for various concrete constructions; having simple and easy process control and non-pollution; resolving the disadvantages of lower polymerization activity of allyl polyether monomer, and resolving the ubiquitous low temperature crystallization problem of allyl polyether-type high performance water reducing agent; and realizing obtaining higher dispersity and preserving degree in low-dosage, particularly, having good dispersion performance on the condition of extremely low water cement ratio.
Owner:ZHEJIANG LAOHUSHAN BUILDING MATERIALS

Lithium battery positive electrode material, preparation method thereof and all-solid-state lithium battery

The invention provides a lithium battery positive electrode material, which comprises a positive electrode active material and a coating layer coating the surface of the positive electrode active material, wherein the coating layer contains Li<1-x>Al<5+y / 3>O<8-x+y> (x is greater than or equal to 0 and less than or equal to 1, and y is greater than or equal to 0 and less than or equal to x), and the mass ratio of the coating layer in the positive electrode material is 0.1%-50%. The positive electrode material provided by the invention does not react with the solid electrolyte LATP at a high temperature, so that the capacity of the positive electrode active material can be normally exerted, and the prepared all-solid-state battery has very good battery performance.
Owner:BYD CO LTD

Method for synthesizing industrial auxiliary N-butylphthalimide

The invention discloses a method for synthesizing an industrial auxiliary N-butylphthalimide. The method comprises the following steps: performing a free radical addition reaction on phthalimide and 1-butene serving as main reacting substrates under an initiator or optical initiation condition to obtain the N-butylphthalimide, wherein the molar ratio of phthalimide to 1-butene in the reacting substrates is 1:1-1:7; the initiator is organic peroxide or inorganic peroxide; the molar ratio of phthalimide to organic peroxide initiator is 5:1-10:1; the molar ratio of phthalimide to inorganic peroxide initiator is 1:1-1:4; the reacting temperature is between normal temperature and 100 DEG C, and the reacting time is 3-24 hours. The method adopts the phthalimide and the 1-butene as raw materials which are low in price and easily available, and has the advantages of mild reacting condition and low production cost.
Owner:安徽翰邦科技咨询有限公司

Preparation method of cinnamic acid or derivatives thereof

The invention discloses a preparation method of cinnamic acid or derivatives thereof. The method comprises the following steps: adding a dichloromethane solution of triethyl phosphonoacetate, sodium chloride and raw material aldehyde into a reaction container, performing room-temperature reaction, adding a saturated water solution of ammonium chloride, stirring, performing organic phase washing, performing reduced pressure treatment to remove a solvent, and performing column chromatography purification to obtain a light yellow oily product; adding a mixed solution of dichloromethane and methanol into a reaction product, stirring, dropwise adding a methanol solution of sodium hydroxide to generate a large quantity of turbid materials, performing reduced pressure distillation on a reaction solution until the reaction solution is dry, removing impurities, extracting, combining organic phases, drying, performing reduced pressure treatment to remove the solvent, and drying in vacuum to obtain a white or light yellow product. According to the method, triethyl phosphonoacetate is adopted as an activating reagent for condensation esterification with aldehyde and then the product is conveniently prepared through alkaline hydrolysis; the reaction can be carried out at room temperature, and the shortcomings of low yield, high reaction temperature, high toxicity and serious pollution in a conventional process are overcome.
Owner:褚朝森

Diminazene aceturate production method

The invention discloses a diminazene aceturate production method. The method comprises the following steps: reacting p-nitrobenzamide with triethylamine and thionyl chloride to synthesize p-nitrobenzonitrile, and carrying out addition, amination, reduction, diazotization, coupling and salt formation on p-nitrobenzonitrile to obtain diminazene aceturate. P-nitrobenzamide is adopted as a raw material to synthesizes p-nitrobenzonitrile, so high temperature reaction is avoided, and industrial production is facilitated; the addition of urea in the diazotization and coupling reactions is in favor of improving the yield; a reaction product obtained after the coupling reaction undergoes water supply and direct pH adjustment without filtering, heating, dissolving or cooling steps, so the reaction steps are simplified, and the reaction time is shortened; and water and methanol are used as solvents in the salt formation, so the volatilization of methanol is reduced, and the crystal form of diminazene aceturate is obviously improved.
Owner:HENAN LINGXIAN SCI & TECHN PHARMA

Method for synthesizing allyl polyether-type high-performance water reducing agent

The invention relates to a synthetic method for an allyl polyether-type high efficiency water reducing agent, belonging to the field of water reducing agent. The synthetic method utilizes allyl polyoxyethylene ether monomer, maleic-anhydride, and a mixture with one or more of (methyl) sodium allylsulfonate, 2-acryl amide-2-methylpropanesulfonic acid, itaconic acid, acrylic acid and acrylamide forobtaining polyether-type high efficiency water reducing agent by initiating one-step polymerization through inorganic peroxides in water solution system, the final structure of the water reducing agent comprises no ester bond, carboxyl, amide, sulfonic group and other functional groups. The synthetic method for an allyl polyether-type high efficiency water reducing agent has the advantages of having applicability for various concrete constructions; having simple and easy process control and non-pollution; resolving the disadvantages of lower polymerization activity of allyl polyether monomer,and resolving the ubiquitous low temperature crystallization problem of allyl polyether-type high performance water reducing agent; and realizing obtaining higher dispersity and preserving degree in low-dosage, particularly, having good dispersion performance on the condition of extremely low water cement ratio.
Owner:ZHEJIANG LAOHUSHAN BUILDING MATERIALS

Hydroxychloroquine sulfate as well as crystal form and preparation method of enantiomer of hydroxychloroquine sulfate

The invention relates to hydroxychloroquine sulfate as well as a crystal form and a preparation method of an enantiomer of hydroxychloroquine sulfate. The invention provides a crystal form A hydroxychloroquine sulfate. An X-ray powder diffraction pattern of the crystal form A hydroxychloroquine sulfate has characteristic peaks at 10.8 degrees, 13.0 degrees, 13.3 degrees, 16.9 degrees, 17.2 degrees, 17.5 degrees, 19.9 degrees, 21.3 degrees, 23.5 degrees, 24.0 degrees and 26.7 degrees +/-0.2 degrees, and does not contain hydroxychloroquine nitrogen oxide; the invention provides a hydroxychloroquine crystal, the X-ray powder diffraction pattern has characteristic peaks at 7.5 degrees, 14.9 degrees, 16.5 degrees, 19.2 degrees, 19.6 degrees, 22.8 degrees, 23.6 degrees and 26.7 degrees+/-0.2 degree; the invention provides an S-hydroxychloroquine sulfate monohydrate, the X-ray powder diffraction pattern has characteristic peaks at 12.2 degrees, 13.0 degrees, 14.9 degrees, 17.8 degrees, 22.7 degrees, 23.3 degrees, 25.0 degrees and 26.2 degrees +/-0.2 degrees; the invention also provides R-hydroxychloroquine sulfate, the X-ray powder diffraction pattern has characteristic peaks at 12.2 degrees, 13.0 degrees, 14.9 degrees, 17.8 degrees, 22.7 degrees, 23.3 degrees, 25.0 degrees and 26.2 degrees +/-0.2 degrees.
Owner:珠海润都制药股份有限公司

Method for preparing baloxavir intermediate

ActiveCN112159380AAvoid use in high temperature conditionsLow costOrganic chemistryKetoneChemical synthesis
The invention belongs to the technical field of chemical synthesis and provides a method for preparing a balosavir intermediate. According to the method disclosed by the invention, cheap and easily available 3-hydroxy-2-(hydroxymethyl)-4H-pyran-4-ketone (a compound shown as a formula I) is used as a starting material; TEMPO oxidation, benzyl protection and hydrolysis reaction are carried out; so that the intermediate compound---3-benzyloxy-4-oxo-4H-pyran-2-formic acid shown as a formula Baloxavir is prepared. According to the method, highly toxic chemicals such as methylsulfonyl chloride and selenium dioxide are prevented from being used, and reaction reagents are common materials. In each step of the method, the temperature is controlled below 60 DEG C, high-temperature reaction is avoided, and the safety coefficient is high. The method has the advantages of short synthesis route, short reaction steps, simple operation, common and easily purchased reagents and low price, and suitability for industrial production.
Owner:HEADING NANJING PHARMTECH CO LTD

Chlorphenesin carbamate and preparation method thereof

The invention discloses chlorphenesin carbamate and a preparation method thereof. The preparation method comprises the step of mixing a compound shown in a formula (1) with ammonium reagent and alkali in an organic solvent in the presence of water at the temperature of 0-40 DEG C. The preparation method in the invention utilizes a raw material containing ammonium ions so as to avoid using of strong pungent ammonia water, improves production safety and is favor of environment protection.
Owner:ZHEJIANG JIUXU PHARMA +1

Polybenzoxazine airgel thermal insulation material and preparation method thereof

The invention discloses a polybenzoxazine aerogel heat thermal insulation material and a preparation method thereof. The polybenzoxazine aerogel heat thermal insulation material is characterized in that a bisphenol A benzoxazine monomer is used as a base raw material, polybenzoxazine is obtained by adopting acid-catalysed ring opening polymerization, and the polybenzoxazine comprises three structures corresponding to a structural formula 1. According to the preparation method, a sol-gel method is adopted; acid catalysis ring opening polymerization is carried out at the normal temperature to obtain gel with a three-dimensional network structure; then the gel is subjected to aging, solvent replacement, CO2 supercritical drying and programmed warming and heat preservation processing to obtainthe polybenzoxazine aerogel heat thermal insulation material. The material disclosed by the invention has excellent performance of low moisture absorption, high intensity, flame retardance, low density, low thermal conductivity and the like; the preparation method is simple in process; prices of raw materials are low; low-temperature ring opening polymerization avoids a high-temperature reaction;the polybenzoxazine aerogel heat thermal insulation material and the preparation method thereof have low requirements for the environment, are short in time consumption in the overall process flow and are suitable for industrial production.
Owner:NAT UNIV OF DEFENSE TECH
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