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70results about How to "Great potential for industrial applications" patented technology

Metal surface nano-composite processing device with stirring head capable of synchronously feeding powder, and method

The invention relates to a processing device for synthesizing a surface layer of a nano-composite material in situ by performing friction stir processing (FSP) on a metal workpiece through a stirring head capable of synchronously feeding powder, and a method. A clamping part 1, a shaft shoulder 2 and a stirring probe 3 of the stirring head can be a rigid whole body or a fastening coaxial separated body; a powder feeding channel A is arranged in the stirring head; the inlet of the channel A is positioned on the side or middle axial position of the clamping part 1; and the outlet of the channelA is positioned on the surface of the middle axial position of the probe 3, which is contacted with the workpiece. During processing, a hydraulic device in a worktable capable of automatically lifting is used for pressurizing along the axial direction B of the stirring head, a rotating shaft drives the stirring head to rotate at high speed and press the workpiece, an external automatic powder feeder feeds sub-micron reinforcing phase powder into a seriously plasticized area C on the surface layer of the workpiece through the powder feeding channel A of the stirring head, and the nano-composite material is synthesized in situ through friction heat. The device is simple, is convenient to operate, is suitable for the composition and structure refining of various metal substrates, and is highin technical and economic benefit and industrial application potential.
Owner:HOHAI UNIV

Preparation method for graphene

InactiveCN105347332AIncrease path lengthIncrease shearing and grinding time and frequencyDefective grapheneSolvent
The invention provides a preparation method for graphene. The preparation method comprises: S1, dispersing natural graphite in a solvent to obtain a graphite suspension; S2, shearing the graphite suspension in a colloid mill; and S3, carrying out centrifugal separation on the sheared graphite suspension to obtain a supernatant, and carrying out vacuum suction filtration and drying on the supernatant to obtain graphene. By using the natural graphite powders which are wide in raw material source and cutting the graphite with the colloid mill, graphite granules can be effectively stripped through a physical action of a severe shear force, a frictional force, high-frequency vibration and high-speed vortex, so that the production efficiency is greatly improved and the graphene can be industrially prepared in batches. Meanwhile, the prepared graphene is few in defect, high in yield, low in cost, good in dispersity and high in quality, and the application range of the graphene is greatly expanded.
Owner:SHANDONG UNIV OF SCI & TECH

Nickel sulfide/carbon nano tube flexible composite thin-film material and preparation method and application thereof

The invention discloses a nickel sulfide / carbon nano tube flexible composite thin-film material and a preparation method and application thereof. The preparation method comprises the steps that urea and nickel nitrate are added into an aqueous solution of ethyl alcohol, then a silicon oxide / carbon nano tube thin film is added, soaked under normal temperature, taken out, placed in a dryer for to react for 10-15h under the temperature ranging from 100 DEG C to 110 DEG C, cooled naturally under room temperature, washed and dried, and then a silicate / carbon nano tube thin film is obtained for use;and deionized water and ethyl alcohol are mixed, Na<2>S is added to serve as a sulfur source, a solution with the concentration ranging from 1mg / mL to 2.5mg / mL is prepared, the silicate / carbon nano tube thin film obtained in the step 1 is soaked in the solution, subjected to a reaction for 10-15h under the condition of 150-200 DEG C, cooled naturally, washed and dried, and then the nickel sulfide / carbon nano tube flexible composite thin-film material is obtained. The nickel sulfide / carbon nano tube flexible composite thin-film material can be directly used as a sodium-ion battery cathode material.
Owner:TIANJIN UNIV

Nitryl asymmetric alpha-diimine nickel complex for preparation of ultrahigh-molecular-weight polyethylene and preparation method and application of nitryl asymmetric alpha-diimine nickel complex

The invention provides a nitryl asymmetric alpha-diimine nickel complex for preparation of ultrahigh-molecular-weight polyethylene and an intermediate, a preparation method and application of the nitryl asymmetric alpha-diimine nickel complex. The nickel complex has a single catalytic active center, regulation of polymer molecular weight and branching degrees can be realized through changing of aligand structure and polymerization conditions, and high catalytic activity, low cost, performance stability and the like are achieved. The preparation method is mild in condition, short in period andsimple in operation condition. The nickel complex can be applied to catalytic vinyl polymerization, the catalytic activity is up to 4.61*10<6>g mol<-1>(Ni) h<-1>, the weight-average molecular weightMw of prepared polyethylene fluctuates in a range of 8.2-32.8*10<5>g mol<-1>, molecular weight distribution is in a range of 1.8-2.8, the remarkable performance of polyethylene molecular weight control is achieved, and the nickel complex can be used for preparation of ultrahigh-molecular-weight polyethylene; obtained polyethylene is high in branching degree, the melt temperature Tm is in a range of 76.9-117.2 DEG C, and accordingly the polyethylene can be used as engineering plastic at a high environment temperature, and a promising industrial application potential is achieved.
Owner:INST OF CHEM CHINESE ACAD OF SCI

Asymmetric diimine pyridine complex with nitro-enhanced thermal stability and catalytic activity as well as preparation method and application of asymmetric diimine pyridine complex

The invention provides a diphenylmethyl-containing asymmetric diimine pyridine complex with nitro-enhanced thermal stability and catalytic activity, and a preparation method and application thereof. The complex has a single catalytic activity center, the molecular weight of a polymer can be regulated and controlled by changing a ligand structure and polymerization conditions, and the complex has the advantages of high catalytic activity, low cost, stable performance and the like. The complex and intermediates thereof have the advantages of mild preparation conditions, short period, simple operation conditions and the like. The asymmetric complex can be applied to a catalyst for ethylene polymerization and has high catalytic activity, and high molecular weight (up to 599.5 kg/mol) linear polyethylene is obtained; especially, the provided iron complex is high in thermal stability, and even at a high temperature of 100 DEG C, the catalytic activity can still be kept at 3.86* 10<6> g*mol<-1>(Fe)*h<-1>. Compared with reported non-nitro substituents (CH3, Cl), the complex has the highest activity and molecular weight. Therefore, the complex can be used at a high environmental temperatureas engineering plastic, and has great industrial application potential.
Owner:INST OF CHEM CHINESE ACAD OF SCI

Fluorine-containing alpha-diimine nickel coordination compounds for preparing polyolefin elastomer, intermediate, preparation method and application thereof

The invention discloses a class of fluorine-containing alpha-diimine nickel coordination compounds for preparing a polyolefin elastomer, and an intermediate thereof, wherein the coordination compoundhas a single catalytic activity center, the molecular weight of a polymer can be regulated and controlled by changing a ligand structure and polymerization conditions, and the coordination compound has the advantages of high catalytic activity, low cost, stable performance and the like. The invention further provides preparation methods of an asymmetric alpha-diimine nickel coordination compound containing a difluoro group, and an intermediate thereof, wherein the two preparation methods have the advantages of mild reaction conditions, short period, simple operation conditions and the like. The invention also provides uses of a metal nickel coordination compound and a catalyst system thereof, wherein the metal nickel coordination compound is used for catalyzing ethylene polymerization, shows good catalytic activity and obtains a polyethylene elastomer material with narrow molecular weight distribution. The obtained polyethylene elastomer material is high in branching degree, has good tensile strength, elongation at break and elastic resilience, is a thermoplastic elastomer material and has great industrial application potential.
Owner:INST OF CHEM CHINESE ACAD OF SCI

Copper-zinc-tin-sulfur-selenium semitransparent solar cell device and preparation method thereof

The invention discloses a copper-zinc-tin-sulfur-selenium semitransparent solar cell device and a preparation method thereof. The preparation method comprises the following steps: taking semitransparent fluorine-doped tin oxide (FTO) or FTO-MoO3 as a back electrode; the copper-zinc-tin-sulfur-selenium semitransparent solar cell device being composed of soda-lime glass, an FTO / FTO-MoO3 back electrode, a copper-zinc-tin-sulfur-selenium absorption layer, a cadmium sulfide buffer layer, a high-resistance intrinsic zinc oxide window layer, a low-resistance indium tin oxide window layer and a nickel-aluminum or silver electrode. The preparation method comprises the following steps of: cleaning commercial FTO conductive glass, evaporating MoO3 with different thicknesses on the FTO conductive glass, and then preparing each layer of film in sequence to obtain the CZTSSe semitransparent solar cell device taking FTO / FTO-MoO3 as the back electrode. The use of the semitransparent back electrode increases many possibilities for the application of the thin-film solar cell, including the generation of electric energy from the back, so that the thin-film solar cell becomes a double-sided device and has great industrial application potential.
Owner:NANJING UNIV OF POSTS & TELECOMM

Recombinant plasmid for producing pipecolinic acid, genetic engineering strain and method

The invention discloses a recombinant plasmid for producing L-pipecolinic acid, a high-yield genetic engineering strain capable of enhancing heterogonous synthesis metabolic pathways of L-pipecolinic acid, and a production method of pipecolinic acid. The invention further discloses a preparation method of the recombinant plasmid and the genetic engineering strain. The strategy of constructing the high-yield genetic engineering strain comprises the following steps: adopting pTrc99a single-plasmid multi-gene tandem expression, linking L-lysine-alpha-oxidase genes (LysoX), glucose dehydrogenase genes (gcd), Pip2C reductase genes (DpkA) and lysine transportase genes (lysQ), optimizing a regulatory element for controlling transcription and translation in front of each gene, transforming the constructed plasmid pLMAIP-05 into competent cells of BL21 (DE3) of essential genes (cadA) in a knockout lysine degradation pathway, thereby obtaining the high-yield genetic engineering strain (MLPR08) capable of enhancing heterogonous synthesis metabolic pathways of L-pipecolinic acid. Due to expression of the lysine transportase, the rate of transporting a substrate L-lysine into the cells is improved, the fermentation time is shortened, and synthesis of the L-pipecolinic acid is further promoted.
Owner:CHONGQING UNIV

Squaramide derivative covalent triazine skeleton polymer and application thereof in catalyzing coupling of carbon dioxide and epoxide to prepare cyclic carbonate

The invention relates to a squaramide-derived covalent triazine skeleton polymer and application thereof in catalyzing coupling of carbon dioxide and epoxide to prepare cyclic carbonate. Squaramide monomers are used as raw materials, a series of squaramide-derived covalent triazine skeleton polymers are synthesized through a high-temperature ionothermal method, and the squaramide-derived covalent triazine skeleton polymers are used as catalysts to prepare cyclic carbonate. According to the method, carbon dioxide and epoxide with different substituent groups are used as raw materials, corresponding cyclic carbonate is synthesized under the conditions that the reaction pressure is 0.1-2.5 MPa, the reaction temperature is 70-110 DEG C and the reaction time is 2-6 hours, and high-selectivity catalysis of synthesis of cyclic carbonate under mild, metal-free and solvent-free conditions is realized. The polymer shows excellent adsorption and conversion dual functions on carbon dioxide, the catalytic activity is not obviously reduced after five catalytic cycles, the problem that a homogeneous catalyst is not easy to separate is solved, and the polymer has a good application prospect.
Owner:QINGDAO UNIV OF SCI & TECH

Metal surface nano-composite processing device with stirring head capable of synchronously feeding powder, and method

The invention relates to a processing device for synthesizing a surface layer of a nano-composite material in situ by performing friction stir processing (FSP) on a metal workpiece through a stirring head capable of synchronously feeding powder, and a method. A clamping part 1, a shaft shoulder 2 and a stirring probe 3 of the stirring head can be a rigid whole body or a fastening coaxial separated body; a powder feeding channel A is arranged in the stirring head; the inlet of the channel A is positioned on the side or middle axial position of the clamping part 1; and the outlet of the channel A is positioned on the surface of the middle axial position of the probe 3, which is contacted with the workpiece. During processing, a hydraulic device in a worktable capable of automatically lifting is used for pressurizing along the axial direction B of the stirring head, a rotating shaft drives the stirring head to rotate at high speed and press the workpiece, an external automatic powder feeder feeds sub-micron reinforcing phase powder into a seriously plasticized area C on the surface layer of the workpiece through the powder feeding channel A of the stirring head, and the nano-composite material is synthesized in situ through friction heat. The device is simple, is convenient to operate, is suitable for the composition and structure refining of various metal substrates, and is high in technical and economic benefit and industrial application potential.
Owner:HOHAI UNIV

Method for constructing super-hydrophobic PVDF nanofiber membrane based on interface self-polymerization and application of super-hydrophobic PVDF nanofiber membrane

The invention provides a method for constructing a super-hydrophobic PVDF nanofiber membrane based on interface self-polymerization and application of the super-hydrophobic PVDF nanofiber membrane, and particularly relates to the technical field of super-hydrophobic materials. The preparation method comprises the following steps: dissolving PVDF in N, N-dimethylformamide to prepare a membrane casting solution, preparing a PVDF nanofiber base membrane by using an electrostatic spinning process, dissolving OTS containing active groups in an organic solvent, sequentially adding nanoparticles, PDMS and a cross-linking agent to prepare an oil-phase reaction solution, soaking the base membrane in ethanol, cleaning with deionized water, drying water drops on the surface of the base membrane by blowing, pouring the oil-phase reaction solution into the surface of the base membrane, introducing a high-hydrophobicity silane polymer into PDMS in situ by utilizing a hydrolysis self-polymerization reaction of OTS on a water-oil interface, pouring away the oil-phase reaction solution, and cleaning and drying a membrane body to obtain the super-hydrophobic PVDF nanofiber membrane. The method is simple in preparation process, does not need a modification device, is excellent in hydrophobicity and stable in property, is suitable for the fields of oil-water separation, self-cleaning coatings, membrane distillation and the like, and has a good industrial application prospect.
Owner:CHINA UNIV OF PETROLEUM (EAST CHINA)
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