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50 results about "Carbon–oxygen bond" patented technology
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A carbon–oxygen bond is a polar covalent bond between carbon and oxygen. Oxygen has 6 valence electrons and prefers to either share two electrons in bonding with carbon, leaving the 4 nonbonding electrons in 2 lone pairs :O: or to share two pairs of electrons to form the carbonyl functional group. =O: Simple representatives of these two bond types are the _OH in alcohols such as the ethanol in beverages and fuels and the C=O in ketones (as well as many other related carbonyl compounds).
Copper-catalyzed formation of carbon-heteroatom and carbon-carbon bonds
InactiveUS6867298B2Cheap and practicalLow costUrea derivatives preparationCarbamic acid derivatives preparationCarbon–oxygen bondHydrazine compound
The present invention relates to copper-catalyzed carbon-heteroatom and carbon-carbon bond-forming methods. In certain embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-nitrogen bond between the nitrogen atom of an amide or amine moiety and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In additional embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-nitrogen bond between a nitrogen atom of an acyl hydrazine and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In other embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-nitrogen bond between the nitrogen atom of a nitrogen-containing heteroaromatic, e.g., indole, pyrazole, and indazole, and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In certain embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-oxygen bond between the oxygen atom of an alcohol and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. The present invention also relates to copper-catalyzed methods of forming a carbon-carbon bond between a reactant comprising a nucleophilic carbon atom, e.g., an enolate or malonate anion, and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. Importantly, all the methods of the present invention are relatively inexpensive to practice due to the low cost of the copper comprised by the catalysts.
Owner:MASSACHUSETTS INST OF TECH
Linear-chain C5/C6 alkane catalyst prepared by sorbitol aqueous phase hydrogenation and preparation method thereof
ActiveCN105289601AHigh selectivityHigh activityHydrocarbon from oxygen organic compoundsMetal/metal-oxides/metal-hydroxide catalystsAlkaneCarbon–oxygen bond
The invention relates to a preparation method of a linear-chain C5 / C6 alkane catalyst prepared by sorbitol aqueous phase hydrogenation. The method comprises the following steps: (1) selecting activated carbon as a catalyst carrier, and drying at the temperature of 100-200 DEG C; (2) adding the dried activated carbon into an ammonium paramolybdate aqueous solution, and drying to obtain a catalyst carrier precursor containing molybdenum; (3) calcining the catalyst carrier precursor containing molybdenum in a muffle furnace to obtain a catalyst carrier containing molybdenum; (4) adding a ruthenium trichloride solution into the catalyst carrier for soaking, and drying to obtain a catalyst carrier precursor containing ruthenium and molybdenum; (5) calcining the catalyst carrier precursor containing ruthenium and molybdenum to obtain an initial catalyst; and (6) performing hydrogen gas reduction on the initial catalyst at the temperature of 250-400 DEG C for 4-8h to obtain the sorbitol aqueous phase hydrogenation catalyst. According to the method, a step soaking method is adopted to inhibit carbon-carbon bond breakage and selectively break carbon-oxygen bonds, so that the selectivity and the excitation capacity of sorbitol hydrodeoxygenation reaction can be improved.
Owner:GUANGZHOU INST OF ENERGY CONVERSION - CHINESE ACAD OF SCI
Carohydrate-Ligand Conjugates and Their Application for the Analysis of Carbohydrate-Protein Interaction
ActiveUS20070287195A1Good reproducibilitySugar derivativesBiological material analysisCarbon–nitrogen bondCarbon–oxygen bond
A novel ligand conjugate which is effectively utilizable for analyzing a function of a protein; a ligand-supporting object; and a method of analyzing a protein. The ligand conjugate has a structure which comprises: a linker compound having a structure represented by the following General Formula (1): (wherein n and p each is an integer of 0 to 6) in which X is a structure comprising one, two, or three hydrocarbon derivative chains which have an aromatic amino group at the end and may have a carbon-nitrogen bond in the main chain, Y is a hydro-carbon structure containing one or more sulfur atoms, and Z is a straight-chain structure comprising a carbon-carbon bond or carbon-oxygen bond; and a sugar which has a reducing end and is bonded to the linker compound through the aromatic amino group.
Owner:JAPAN SCI & TECH CORP +1
Arc-extinguishing insulation material molded product and gas circuit breaker including the same
ActiveUS20150357137A1Promote decompositionIncrease pressureHigh-tension/heavy-dress switchesAir-break switchesHydrogenHydrogen atom
The present invention relates to an arc-extinguishing insulation material molded product provided in the vicinity of a contact point between contactors in a gas circuit breaker. The arc-extinguishing insulation material molded product includes a polymer which contains a carbon-oxygen bond in the main chain, and in which a part of or all of terminal atoms are non-hydrogen atoms.
Owner:MITSUBISHI ELECTRIC CORP
Copper-catalyzed formation of carbon heteroatom and carbon-carbon bonds
InactiveUS20050215794A1Cheap and practicalLow costUrea derivatives preparationCarbamic acid derivatives preparationCarbon–oxygen bondHydrazine compound
Owner:MASSACHUSETTS INST OF TECH
Production Method Of Deoderized Polyoxyalkylene-Modified Polysiloxane Composition
To provide a method of producing a polyoxyalkylene-modified polysiloxane composition that is free of acid-mediated carbon-oxygen bond and silicon-oxygen bond cleavage, that is substantially deodorized and also does not generate odor with elapsed time, and that is therefore well suited for use in cosmetic applications, e.g., for hair cosmetics, skin cosmetics, and so forth. A production method of this invention is characterized by removing the odor-causing substance from a polyoxyalkylene-modified polysiloxane composition that has been synthesized by a hydrosilylation reaction, by subjecting the polyoxyalkylene-modified polysiloxane composition to a hydrolysis treatment in the presence of an acidic inorganic salt that is a solid at 25° C. and gives a specific pH at 25° C. in aqueous solution; for example, potassium hydrogensulfate.
Owner:DOW TORAY CO LTD
Aminated graphene oxide
InactiveCN109250710AMaintain lamellar structureEasily brokenCarbon compoundsCarbon–oxygen bondBiological activation
The invention provides aminated graphene oxide preparing from graphene oxide having undergone surface hydroxyl activation and an ammonia source. According to the invention, the graphene oxide having undergone surface hydroxyl activation is used as a raw material, and the ammonia source is directly added for amination modification; and after a hydroxyl group on the surface of the graphene oxide isactivated, a carbon-oxygen bond becomes easy to break, so the lamellar structure of the graphite oxide can be well maintained and original characteristics can be reserved.
Owner:SHANDONG OBO NEW MATERIAL CO LTD
Production method of deodorized polyoxyalkylene-modified polysiloxane composition
Owner:DOW CORNING TORAY CO LTD
Production method of deodorized polyoxyalkylene-modified polysiloxane composition
ActiveUS8877886B2Reduce the smellCosmetic preparationsSilicon organic compoundsInorganic saltsCarbon–oxygen bond
Owner:DOW TORAY CO LTD
Preparation method for aminated graphene oxide
InactiveCN109250711AReduce the temperatureShorten the timeMaterial nanotechnologyCarbon compoundsCarbon–oxygen bondBiological activation
The invention provides a preparation method for aminated graphene oxide. The preparation method comprise a step of subjecting an activated graphene oxide solution, an ammonia source and an organic solvent to mixing and a reaction so as to obtain the aminated graphene oxide, wherein the activated graphene oxide comprises graphene oxide having undergone surface hydroxyl activation. According to theinvention, the graphene oxide having undergone surface hydroxyl activation is used as a raw material, and the ammonia source is directly added for amination modification; after a hydroxyl group on thesurface of the graphene oxide is activated, a carbon-oxygen bond becomes easy to break, so the desired temperature and time of amination are greatly reduced, and a modification reaction can be carried out under mild conditions at a low temperature; and thus, the lamellar structure of the graphite oxide can be well maintained and original characteristics can be reserved. Compared with a two-step-reaction amination process, the method of the invention has the following advantages: the surface-activated graphene oxide is directly utilized as the reaction raw material, so one step of reaction isomitted, and reaction time and energy consumption are reduced.
Owner:SHANDONG OBO NEW MATERIAL CO LTD
A boron doping modified soft carbon coating negative electrode material with high stability under high and low temperature environment and a preparation method thereof
ActiveCN109167025AEasy to operateUnique preparation processCell electrodesSecondary cellsCarbon–oxygen bondCarbonization
The invention relates to the field of lithium batteries, and discloses a boron doped modified soft carbon coating negative electrode material with high stability under a high-low temperature environment and a preparation method thereof. An amorphous carbon-carbon lay is formed on that surface of a negative electrode substrate aft carbonization by a soft carbon source, boron oxide is generated by decomposing a boron compound at a high temperature, the reaction of the boron oxide with the amorphous carbon and the surface of the negative electrode substrate is controlled, and a composite structure such as a boron-carbon bond and a boron-carbon-oxygen bond is for on the surface of the negative electrode material at a high temperature. 1, that soft carbon coat can reduce the impedance of the material under the low temperature, improve the liquid absorption performance, increase the low-temperature discharge voltage platform and greatly improve the low-temperature performance of the material; 2. By the catalysis of boron, the degree of graphitization of the cathode material is increased by reducing the surface defects, so that the specific surface area is greatly reduced, and the side reaction of the cathode material with the electrolyte at high temperature is reduced by the smaller specific surface area, and the performance at high temperature is obviously improved.
Owner:HUZHOU CHUANGYA POWER BATTERY MATERIALS
Preparation method of alkyl borate
InactiveCN107573369AWide variety of sourcesEasy to manufactureGroup 3/13 element organic compoundsCarbon–oxygen bondAlcohol
The invention provides a preparation method of alkyl borate. The preparation method comprises the following step: reacting by taking alkyl tosylate and bisdiboron shown as a formula I-a as raw materials under the action of a silver catalyst and alkali to obtain the alkyl borate shown as the formula I. According to the preparation method provided by the invention, commercially-available silver saltis directly adopted for participating into the reaction, a reaction system and a feeding mode are simple, and no ligand needs to be added. The used bisdiboron is insensitive to air and water and further is more convenient in actual application. The alkyl tosylate as the raw material can be conveniently prepared from alkyl alcohol and the raw material is wide in source; meanwhile, first-stage or second-stage alkyl borate is obtained by silver catalysis direct carbon-oxygen bond fission of the alkyl tosylate and the bisdiboron; the reaction has good functional group compatibility.
Owner:UNIV OF SCI & TECH OF CHINA
A boron-doped negative electrode material with good high-temperature performance and a solid-phase preparation method thereof
ActiveCN109148843ASimple preparation processUnique structural designCell electrodesLi-accumulatorsDopantCarbon–oxygen bond
The invention relates to the field of lithium batteries, and discloses a boron-doped negative electrode material with good high temperature performance and a solid-phase preparation method thereof. Asa boron oxide compound is used as a dopant, the boron oxide compound is decomposed to generate boron oxide at high temperature directly through a solid-phase reaction, and the boron oxide is controlled to react with the surface of the negative electrode material. The structure of the material of the invention is characterized in that the composite structure of a boron-carbon bond and boron-carbon-oxygen bond and the like is formed on the surface of the negative electrode material from the original defect state. By surface modification, on the one hand, On the other hand, the surface defects of the negative electrode material can be reduced by the composite reaction of boron oxide and the surface of the negative electrode material, so that the specific surface area of the negative electrode material can be greatly reduced, and the side reaction of the negative electrode material with the electrolyte at high temperature can be reduced by the smaller specific surface area, and the high temperature performance can be obviously improved.
Owner:HUZHOU CHUANGYA POWER BATTERY MATERIALS
System and method for converting ambient carbon dioxide to particulate carbon and oxygen
InactiveUS20110290661A1Reduce wear rateExtend the life cycleCellsGas treatmentSolid carbonCarbon–oxygen bond
A system and method is described to convert ambient carbon dioxide (CO2) to graphite and oxygen by splitting the carbon oxygen bonds. By using this process, CO2 from point sources or from ambient air can be reduced or effectively eliminated, and thus the system can play an important role in the fight against CO2 emissions and global warming. The system first introduces CO2 and electrolyte solution to one or a series of specially designed pipes rotating pipes to create induction inside the pipes, resulting in breaking of the carbon-oxygen bonds and production of solid carbon and gaseous oxygen. The solid carbon and gaseous oxygen are then separated.
Owner:NIIOKA YOSHIO
Iridium complex with double-emission properties, method for preparing iridium complex and application thereof
ActiveCN107955041AApparent double emissionRealize detectionIndium organic compoundsFluorescence/phosphorescenceIridiumCarbon–oxygen bond
The invention provides an iridium complex with double-emission properties, a method for preparing the iridium complex and application thereof. A structural formula of the iridium complex is shown. Theiridium complex comprises a metal iridium center, a neutral N^N auxiliary ligand and two cyclic C^N ligands. The C^N ligands contain 4-aminodiphenyl ether groups. The iridium complex, the method andthe application have the advantages that the ionic type iridium complex has the obvious double-emission properties; carbon oxygen bonds can be ruptured after the carbon oxygen bonds in the ligands actwith hypochlorite ions, accordingly, excitation states and photophysical properties of the iridium complex can be changed, and the hypochlorite ions can be detected; phosphorescence iridium complex materials have important application prospects in the aspect of biology.
Owner:NANJING UNIV OF POSTS & TELECOMM
Indole derivative and preparation method thereof
ActiveCN110256443ASimple and fast operationMild conditionsOrganic chemistryCarbon–oxygen bondCoupling
The invention provides an indole derivative and a preparation method thereof. The preparation method includes the following steps: mixing a compound shown in a formula I, an additive and a solvent, carrying out a reaction under the conditions of nitrogen or argon and visible light to obtain the indole derivative. In the atmosphere of nitrogen or argon, the compound of the formula I is excited by visible light to be subjected to homolysis of a carbon-oxygen bond, [1,6]-H transfer is carried out, and finally the indole derivative is synthesized by intramolecular free radical coupling and a dehydration reaction. The whole process does not need the participation of a photocatalyst, has the advantages of simple operation, mild condition and high yield, is in line with atomic economy and environmental protection, and has high reference value for industrial preparation of the indole derivative.
Owner:GUANGZHOU UNIVERSITY OF CHINESE MEDICINE
Method of recycling rubber powder of junked tires through activation
ActiveCN105330922AImprove integrityReduce sulfur contentPlastic recyclingPolymer scienceCarbon–oxygen bond
The invention relates to the technical field of recycle of rubber powder of junked tires, in particular to a method of recycling the rubber powder of the junked tires through activation. Particles of the junked tires and quick lime are subjected to heat treatment under the action of water; microwave radiation is conducted to damage sulfur-sulfur bonds and sulfur-carbon bonds; in combination with bitumen, carbon-carbon bonds and carbon-oxygen bonds not subjected to microwave radiation are repaired; in combination with the ultrasonic effect in an environment where ammonium hydroxide exists, the rubber powder is pre-activated; in combination with ultraviolet irradiation and addition of polyacrylamide and a desulfurizing agent, in the grinding process through a grinding machine, the sulfur-sulfur bonds and the sulfur-carbon bonds are completely damaged, integrity of the carbon-carbon bonds and the carbon-oxygen bonds is protected, the sulfur content in the rubber powder is substantially lowered, the tensile strength of a rubber product prepared by mixing the rubber powder and natural rubber reaches 28-31 MPa, the tensile elongation at break is increased by 30% or above compared with that of a traditional product, and the performance of the rubber product is improved by 1-2.7% compared with that of natural rubber.
Owner:贵州华宇橡胶科技有限公司
Acid-functionalized nanoparticle catalyst and catalyzed reactions using the same
InactiveUS8877951B2Organic compound preparationOrganic-compounds/hydrides/coordination-complexes catalystsCarbon–oxygen bondFunctionalized nanoparticles
Owner:KANSAS STATE UNIV RES FOUND
Preparation method of high-plastic edible plasticine
The invention relates to the technical field of children's toy preparation, in particular to a preparation method of high-plastic edible plasticine. The method comprises the steps that bamboo fiber issoaked in a hot acetic acid solution, and chloracetylated cellulose is obtained; the chloracetylated cellulose is subjected to ultrasonic treatment and centrifugalization, and chloracetylated nanocellulose is obtained; a chitosan solution and an agar solution are treated to obtain porous gel, the porous gel is soaked in mixed suspension liquid of the chloracetylated nanocellulose and corn starch,and a plasticine base material is obtained; the plasticine base material, guar gum, maltitol and other raw materials are mixed and heated, and the high-plastic edible plasticine is obtained. Carboxylon a molecular chain and amidogen on amidogen generate ion crosslinking, the viscoplastic property of the plasticine is improved, a carbon-carbon bond, a carbon-oxygen bond and a carbon-hydrogen bondof a blend are difficult to break, the thermal stability of the plasticine is improved, when the plasticine is eaten by children by mistake, the plasticine is turned to be powdery starch polysaccharide substances rapidly, and cannot cause physiological injury to children, and the application prospect is wide.
Owner:钱万琦
Preparation method for substituted isocoumarin derivatives
ActiveCN110128393ARaw materials are easy to getHigh yieldOrganic chemistryCarbon–oxygen bondOrganic solvent
The invention discloses a preparation method for substituted isocoumarin derivatives. The method comprises the following steps: a novel carbon-carbon bond and a carbon-oxygen bond are constructed while a carbon-carbon bond and a carbon-hydrogen bond are cut, a base, dichloro(p-cymene)ruthenium(II) dimer, 2,4,6-trimethylbenzoic acid and sulfur ylide are reacted in an organic solvent, and thereforethe substituted isocoumarin derivatives are prepared. According to the method provided by the invention, the raw materials used in the method are easy to obtain, the yield is high, the reaction conditions are mild, the reaction time is short, the substrate range is wide, the reaction specificity is strong, and the post-treatment is simple and green.
Owner:HUAQIAO UNIVERSITY
Preparation method and application of modified nano calcium carbonate
ActiveCN109627805AMolecular chain lengthEasy to controlPigment treatment with macromolecular organic compoundsLubricant compositionCarbon–oxygen bondWhiskers
The invention discloses a preparation method and application of modified nano calcium carbonate, and belongs to the technical field of preparation of modified calcium carbonate. Synthesis of the modified nano calcium carbonate comprises the following steps that calcium carbonate crystal whiskers are put into a vacuum oven at 105 DEG C to be dried for 2 hours, so that the water content is between 0.3-0.6%; a macromolecular modifier ABM is diluted by using an acetone solvent, and a mixed solvent is obtained after uniform mixing; the dried calcium carbonate crystal whiskers are placed into a three-roller continuous modification machine, the mixed solvent is slowly added under medium-speed stirring, and the modified nano calcium carbonate is obtained after stirring is carried out for 30 min. According to the modified nano calcium carbonate, carbon oxygen bonds with stable performance can be introduced on the surface of filler, and in the high-temperature thermal aging process, the modifiednano calcium carbonate can be added into lubricating grease by scarifying the carbon oxygen bonds in molecules to protect other chemical bonds in the lubricating grease, so that the aging speed of alubricating grease system is reduced, and the high temperature resistance is improved.
Owner:GUANGXI UNIV +1
Preparation method of 2,4-di-substituted-1,3,5-triazine
ActiveCN107759530AWide variety of sourcesEasy to getOrganic chemistryPotassium iodinePotassium carbonate
The invention discloses a method for preparing 2,4-di-substituted-1,3,5-triazine. The method comprises the specific step: with substituted formamidine hydrochloride as a reaction substrate an iodine-containing compound as a catalyst, tert-butyl hydroperoxide as an oxidant, inorganic base as an acid binding agent and aliphatic ether as an organic solvent (also used as a carbon source), carrying outcarbon-hydrogen and carbon-oxygen bond deletion, nucleophilic addition, deaminizing condensation and oxidative aromatization reaction to obtain a 2,4-di-substituted-1,3,5-triazine compound, wherein achemical structural general formula of the substituted formamidine hydrochloride is shown in the description; the iodine-containing compound is selected from one of potassium iodide (KI), tetrabutylammonium iodide (TBAI), elemental iodine (I2) and N-iodosuccinimide (NIS); the inorganic base is selected from one of anhydrous potassium carbonate, anhydrous sodium carbonate, cesium carbonate, potassium hydroxide and potassium tert-butoxide; and the aliphatic ether is selected from one of methyl tert-butyl ether, ethyl ether and ethylene glycol dimethyl ether. The preparation method disclosed bythe invention has the characteristics of easily-obtained raw materials, low price and low toxicity of a catalyst, wide range of the substrate, simplicity and convenience in operation, greenness, environmental protection and the like.
Owner:ZHENGZHOU UNIVERSITY OF LIGHT INDUSTRY
Method for synthesizing 2-methyl-8-methoxy benzofuran [2, 3-b] pyridine
ActiveCN110003227AAvoid it happening againLow priceOrganic chemistryCarbon–oxygen bondHydrazine compound
The present invention discloses a method for synthesizing 2-methyl-8-methoxy benzofuran [2, 3-b] pyridine. The method comprises the steps of under alkaline conditions, forming a carbon-oxygen bond through a nucleophilic substitution reaction of 2-chlorine-3-nitro-6-methyl pyridine and guaiacol; under the catalysis of palladium and carbon, carrying out hydrazine hydrate to reduce nitro to generatecorresponding aromatic amine; and carrying out cyclization of the aromatic amine under the action of isoamyl nitrite to synthesize the 2-methyl-8-methoxy benzofuran [2, 3-b] pyridine. As no need to use expensive 2-amino-3-bromine-6-Methylpyridine and 2, 3-dimethoxy phenylboronic acid serving as raw materials, the method has an obvious cost advantage; and meanwhile, the nucleophilic substitution reaction and a diazotization reaction which are simple to operate are adopted in the first two steps of the method, therefore a Suzuki coupling reaction with higher operation requirements and needing corresponding noble metal palladium as a catalyst can be replaced. The method has the advantages of high reaction yield, low production cost, simple post-treatment process and high product purity, and is suitable for process scale up.
![Method for synthesizing 2-methyl-8-methoxy benzofuran [2, 3-b] pyridine](https://images-eureka.patsnap.com/patent_img/32806ef1-da91-4cfc-aa41-59e5fdcef53f/190424145458.png "Method for synthesizing 2-methyl-8-methoxy benzofuran [2, 3-b] pyridine")
![Method for synthesizing 2-methyl-8-methoxy benzofuran [2, 3-b] pyridine](https://images-eureka.patsnap.com/patent_img/32806ef1-da91-4cfc-aa41-59e5fdcef53f/190424145503.png "Method for synthesizing 2-methyl-8-methoxy benzofuran [2, 3-b] pyridine")
![Method for synthesizing 2-methyl-8-methoxy benzofuran [2, 3-b] pyridine](https://images-eureka.patsnap.com/patent_img/32806ef1-da91-4cfc-aa41-59e5fdcef53f/190424145508.png "Method for synthesizing 2-methyl-8-methoxy benzofuran [2, 3-b] pyridine")
Owner:XINXIANG RUNYU NEW MATERIAL TECH CO LTD
Substrate for cell culture
ActiveUS8835173B2Increase speedHigh speed transmissionBioreactor/fermenter combinationsBiological substance pretreatmentsCarbon–oxygen bondAdhesion process
Owner:DAI NIPPON PRINTING CO LTD
Activation method of graphene oxide
ActiveCN107089657AMaintain lamellar structureMaintain propertiesCarbon compoundsActivation methodCarbon–oxygen bond
The invention provides an activation method of graphene oxide. The activation method comprises the following steps: firstly, dispersing graphene oxide in a polar solvent to obtain a graphene oxide solution; secondly, mixing the graphene oxide solution obtained in the previous step, an activating agent and an acid-binding agent to obtain a reaction system; lastly, under an anaerobic condition, heating the reaction system obtained in the previous step for reacting to obtain activated graphene oxide. By adopting the activation method, hydroxyl on the surface of the graphene oxide is activated under a mild condition, and an easy-leaving radical is formed by combining the activating agent and the hydroxyl on the surface of the graphene oxide, so that a carbon-oxygen bond on the surface of the graphene oxide is activated, and the difficulty in subsequently modifying a covalent bond on the surface of the graphene oxide is lowered; an intermediate with higher activity is provided for the surface functional modification of the graphene oxide, so that subsequent surface modification can be performed without extreme conditions, energy consumption is lowered, and the lamellar structure of graphene can be kept well, thereby keeping the characteristic of the graphene.
Owner:SHANDONG OBO NEW MATERIAL CO LTD
Preparation method of color-variable anti-counterfeiting low-toxicity inkpad
The invention discloses a preparation method of color-variable anti-counterfeiting low-toxicity inkpad, and belongs to the technical field of chemical engineering. Carboxyl on molecular chains of bamboo charcoal viscose fibers provided by the invention and amino on chitosan can be subjected to high ionic cross-linking action; porous rubber powder is taken as a framework raw material of the inkpad,high hydrogen bond interaction between guar gum, cellulose, chitosan and agar is achieved, and the guar gum, the cellulose, the chitosan and the agar can all absorb water vapor in the air to form a reticular water-retaining structure of saturated hydrogel, so that the inkpad forms a uniform system, is not dried easily, and can be stored for a long time; methyl red is added as an anti-counterfeiting reversible pigment, and fills the gel inkpad through cocrystallization, and carbon-carbon bonds, carbon-oxygen bonds and carbon-hydrogen bonds in the inkpad are difficult to break through hydrogenbond action between hydroxyl of the chitosan and hydroxyl of the agar the cellulose and through action between amino and hydroxyl of the chitosan, so that dehydration of the inkpad is more difficult,and thermal stability of the inkpad is improved.
Owner:周建兵
Highly durable antifogging coating film and coating composition
ActiveUS20190055410A1Good anti-fogging propertiesExcellent waterproofnessAntifouling/underwater paintsPolyether coatingsColloidal silicaCarbon–nitrogen bond
The present invention pertains to a coating film, and more particularly, to an antifogging coating film having excellent antifogging properties, ability to retain antifogging properties, and water resistance. The coating film according to the present invention contains a metal oxide (A) and a hydrophilic compound (B), wherein the elemental concentration ratio (C1s / M), which is between the element C and a metal element and which is obtained from a metal (M) spectrum derived from the metal oxide and a C1s spectrum in an elemental analysis of the surface using XPS, is within the range of 0.2-10. The relative elemental concentration of the element C obtained from a C1s spectrum derived from carbon-oxygen bonds and / or carbon-nitrogen bonds in elemental analysis of the surface using XPS may be within the range of 5-50 atomic %. The metal oxide may be colloidal silica. The coating film according to the present invention can be particularly preferably used as an antifogging coating film and a coating film for automotive exterior parts.
Owner:ASAHI KASEI KK
Processing technology of modified carbon fibers
InactiveCN110396732AIncrease carbon-oxygen bondIncreased shear strengthCarbon fibresSurface reaction electrolytic coatingFiberCarbon–oxygen bond
The invention discloses a processing technology of modified carbon fibers. The processing technology comprises the following steps of a, filament return and thread collection, wherein a protofilamentis selected, after splitting, a new filament and an old filament are connected with a heat-resistant fiber, and the mixture is erected on a thread collection plate; b, primary drying, wherein the thread collection plate and the protofilament are conveyed into a drying device for drying, and the moisture in the protofilament is removed; c, preoxidation; d, carbonization; e, electrolytic oxidation modification; f, soaking modification. The processing technology has the advantages that an electrolytic oxidation mode is adopted for modifying the surfaces of the carbon fibers, active functional groups are introduced into the surfaces of the carbon fibers, the carbon oxygen bonds of the surfaces of the carbon fibers are increased, the contact compactness of the carbon fibers and the surface of acomposite material in the compounding process is improved, and the increase and decrease shearing strength of the synthesized composite material is improved; the interface bonding force of a bondingface is improved, and accordingly the tensile strength and impact-resistance strength of the carbon fiber and resin base material composite material is improved.
Owner:DATONG XINCHENG NEW MATERIAL CO LTD
Poly-bisacrylamido cationic compound and preparation method thereof
ActiveCN105820278AHigh cationic degreeGood water solubilityWater/sewage treatment by flocculation/precipitationSolubilityCarbon–oxygen bond
The invention relates to a poly-bisacrylamido cationic compound and a preparation method thereof. The preparation method comprises the following steps: carrying out amidation reaction, chloromethylation reaction, ring-opening reaction and quaterization reaction, preparing two different cationic compounds, and carrying out water solution polymerization to obtain the cationic organic high-molecular polymer. The molecules contain cations, and also contain amido groups, ester groups, carbon-oxygen bonds, large pi bonds and water-soluble hydroxy groups. The cation degree and water solubility of the polymer are greatly enhanced as compared with common cationic compounds. Since the organic matter content in sewage (waste water) is greatly enhanced along with the development of the modern industry and the enhancement of the living standard, the organic matter particle surface is usually negatively charged, and the cationic high-molecular flocculant can perform the electric neutralization and adsorptive bridging functions on particles in water, so that the particles in water are destabilized and flocculated, thereby being beneficial to settling and filter dehydration.
Owner:SHAANXI UNIV OF SCI & TECH
Electrolyte, lithium ion secondary battery and electric vehicle
ActiveCN109786838AInhibitory responseImprove performanceSecondary cells servicing/maintenanceHigh temperature storageTectorial membrane
The invention provides electrolyte, a lithium ion secondary battery and an electric vehicle. The electrolyte comprises a solvent, lithium salt and additives; the additives comprises aromatic urea compound, and the chemical formula of the aromatic urea compound is as shown in description. By importing the aromatic urea compound in the electrolyte, the benzene ring and carbon-oxygen bond in the aromatic urea compound can form a layer of protective film on a surface of the electrode material through chemical reaction. The protective film is stable in the high-temperature environment and the battery circulating process, thereby effectively prohibiting the reaction of the electrolyte on the surface of the electrode material, and prohibiting the digestion of cathode material metal; the high-temperate circulating performance and the storage performance of the lithium ion battery are improved, the gas production in high-temperature storage is prohibited, the comprehensive performance of the battery under high voltage is improved, and then the problem that the battery is in expansive deformation, internal short-circuiting and electrolyte leakage is avoided.
Owner:SVOLT ENERGY TECHNOLOGY CO LTD
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