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104results about How to "Change crystal structure" patented technology

Preparation method for element-doping manganese bioxide electrode material for super capacitor

The invention relates to a preparation method of an element doped manganese dioxide electrode material for a supercapacitor; the preparation method is characterized in that the high-energy ball milling method is adopted to mix any one of Al, Ti, Ni and Fe with manganese atoms in manganese dioxide according to the ratio of 0.05: 0.95 and then the mixture is placed in a high-energy ball milling tank, a ball milling medium is selected from agate balls with the different diameters, ratio of grinding media to material is 20:1, ethanol is added for preventing the agglomeration, the ball milling speed is 250 turns/minute, the ball milling time is controlled to be 15 hours; products are taken out after the ball milling tank is cooled to the room temperature, the drying at the constant temperature of 80 DEG C is carried out in a drying box for 48 hours; the powder after the drying is ground in an agate mortar to obtain the element doped manganese dioxide supercapacitor electrode material prepared by ball milling. The preparation method has low cost and simple preparation technology, the obtained element doped manganese dioxide electrode material has uniform distribution, high specific capacitance and good cycle stability; the preparation method can be applied in occasions which need power supply with neutral electrolyte, high stability and high power density.
Owner:SHANGHAI SECOND POLYTECHNIC UNIVERSITY

Metal surface nanometer powder permeating method based on laser induction shock waves

The invention relates to a metal surface nanometer powder permeating method based on laser induction shock waves. The method comprises the following steps that base materials are pretreated; a machining surface is covered with an absorbing layer; a base metal surface is covered with the absorbing layer; a restraining layer is exerted on the base metal surface; pre-impact life-extension treatment is carried out on the base metal surface on which the restraining layer is exerted; impact life extension is carried out on the base metal surface subjected to the impact life extension treatment; and base metal materials are subjected to aftertreatment. In the process of covering the machining surface with the absorbing layer, in a clean room, a thin plate is taken, and an opening with the needed size and shape is shorn out in the middle; the thin plate is attached to the surface of the absorbing layer, and the middle of the thin plate is evenly coated with nanometer particles; and the rest is removed thoroughly, and a particle coating layer with the thickness equal to that of the thin plate is formed on the surface of the absorbing layer. According to the metal surface nanometer powder permeating method, a crystal structure, orientation distribution and metal surface elementary components on the base metal surface are obviously changed, the hardness, the fatigue life, the abrasion resistance and the corrosion resistance of the metal surface are effectively improved, operation is simple, and cost is low.
Owner:SHENYANG LIMING AERO-ENGINE GROUP CORPORATION

Method for enabling metal surface to penetrate nano powder by laser-induced impact

The invention belongs to the technical field of metal material surface treatment, and particularly relates to a method for enabling a metal surface to penetrate nano powder by laser-induced impact. The method comprises the following steps: coating on the surface of an absorption layer to form a nano particle coating layer, and covering the nano particle coating layer on a working end surface of a target material; applying a restraint layer on the absorption layer; enabling a to-be-treated substrate metal surface to face towards a laser beam, firstly carrying out pre-penetration treatment and then carrying out penetration treatment on the to-be-treated substrate metal surface; and enabling the substrate metal surface obtained by cleaning to penetrate into nano particles, thereby improving the hardness of the substrate metal surface. The method is simple in operation process, and is a metal surface treatment technology which is low in cost, efficient and green. According to the method, element components of the metal substrate surface are improved, the elements of the metal surface are re-distributed, and lattice distortion, dislocation and grain refinement are caused, so that the strength and the hardness of the metal surface are improved, and thus, the abrasion-resistance of a metal component is improved and a fatigue life of the metal component is prolonged.
Owner:SHENYANG LIGONG UNIV

Perovskite type composite metal oxide oxygen carrier as well as preparation method and application thereof

The invention belongs to the technical field of oxygen carriers, and discloses a perovskite type composite metal oxide oxygen carrier and a preparation method and application thereof. The perovskite type composite metal oxide oxygen carrier is of a perovskite structure, the general formula of the oxygen carrier is La<1-x>Ce<x>FeO<3>, and x is greater than 0 and less than or equal to 1. A sol-gel method is adopted in the preparation method, and the preparation method comprises the following steps: firstly, taking lanthanum nitrate, cerium nitrate and ferric nitrate as precursors, and preparinga solution from the precursors and a complexing agent; then evaporating to remove water, and converting an obtained transparent sol into a viscous gel; and aging and roasting to obtain the composite metal oxide oxygen carrier with a perovskite structure. When the perovskite type composite metal oxide oxygen carrier is chemical-looping methane reforming reaction, methane can be partially oxidized with high activity and high selectivity to prepare synthesis gas; meanwhile, the oxygen carrier is reduced to be in a low valence state, the reduced oxygen carrier can react with carbon dioxide or water vapor to be oxidized to be in a high valence state, lattice oxygen is obtained again, cyclic regeneration of the oxygen carrier is achieved, and meanwhile carbon dioxide is converted into carbon monoxide or the water vapor is converted into hydrogen gas.
Owner:TIANJIN UNIV +1

Steel pipe installing and expanding equipment with high-temperature heating and remodeling functions

InactiveCN104588520AThere will be no phenomenon of being stuck in the steel pipeFast expansionShaping toolsCouplingArchitectural engineering
The invention discloses steel pipe installing and expanding equipment with high-temperature heating and remodeling functions. The equipment comprises a base. The base is provided with a baffle, a transition rail, a rotating clamping device, a guide rail and a telescopic cylinder in sequence from left to right. A sliding block is movably connected to the guide rail. One end of the sliding block is connected with the output end of the telescopic cylinder. A number one motor is fixedly connected to the sliding block. An output shaft of the number one motor is connected with an expansion die through a coupler. A steel pipe is fixedly connected to the rotating clamping device and a clamping plate. The number one motor and the telescopic cylinder are matched to enable the expansion die to rotate while advancing, and the expansion speed of the steel pipe is increased; similarly, the phenomenon that the expansion die gets stuck in the steel pipe is avoided, the steel pipe rotates reversely under driving of a number two motor, and a spray gun is matched, so that the part, to be expanded, of the steel pipe is heated, the crystal structure in the part, to be expanded, of the steel pipe is changed, expanding is easier, and burst of the steel pipe is avoided.
Owner:杜玉华

Method for synthesizing SAPO-35 molecular sieve by using bi-template

The invention discloses a method for synthesizing an SAPO-35 molecular sieve by a two-mode agent, which is characterized in that the method comprises the steps of mixing aluminum source, phosphorus source, silicon source and an organic template to glue at the temperature of room temperature to 100 DEG C and preparing into the reaction mixture with the molar ratio components of a1R1+a2R2: Al2O3: bP2O5: cSiO2: dH2O, wherein R1 and R2 are the organic templates, the value of a1 is 0.5-1.8, the value of a2 is 0.1-1.0, the value of b is 0.5-1.5, the value of c is 0.05-2.5, and the value of d is 10-150; the reaction mixture undergoes hydrothermal crystallization for 0.5-500 hours at the temperature of 150-250 DEG C and the crystallization product is recovered. The R1 is hexamethylene imine, and the R2 is any of cyclohexane, piperidine, tropine, diethylamine and triethylamine. The method provided by the invention can synthesize the high-crystallinity SAPO-35 molecular sieve in a relatively wide silica content range. The SAPO-35 molecular sieve synthesized by the method of the invention is applicable to the hydrocarbon conversion technology. Applied to the olefin preparation reaction by methanol dehydration, the molecular sieve has very low alkane selectivity and high product yield of ethylene and propylene.
Owner:CHINA PETROLEUM & CHEM CORP +1

Sucrose succedaneum and preparation method thereof

The invention provides a cane sugar substitute and the preparation method of the substitute, of which the elements are: 90 percent to 97 percent of glucose, 2 percent to 8 percent of maltodextrin and 0.5 percent to 3 percent of sucralose. The technique is that: the maltodextrin and the sucralose are added into a vessel to mix with deionized water, then the temperature is raised to 50 DEG C to 65 DEG C for dissolution and the mixture is stirred, then active carbon is added and the mixture is kept warm for 40 minutes to 50 minutes and filtered when still being warm, and the filtrate respectively is converged to a reserve tank which is provided with jacket heating; the glucose is crushed and sent to a spraying fluidized-bed with the temperature of the bed layer being 30 DEG C to 85 DEG C, and the well prepared sucralose solution is firstly pumped in and continuously sprayed for decentralization, then the well prepared maltodextrin solution is pumped in and continuously sprayed for granulating, and the cane sugar substitute with good decorated surface is prepared. The proposal takes glucose and sucralose as main raw materials to make the sweetness of the product be 2 times to 12 times of the sweetness of ordinary cane sugar by making sweetness decoration and packing on the surface. The preparation process of the invention is easy and simple, thereby being applicable for scale production.
Owner:DALIAN SANTAI BIOLOGICAL TECH

Method for preparing phosphinic acid modified aluminum hydroxide flame retardant agents

The invention discloses a method for preparing phosphinic acid modified aluminum hydroxide flame retardant agents, which is characterized by comprising the following steps that: the aluminum hydroxide is taken, the organic solvent glacial acetic acid is taken according to the proportion being 10 to 15 times of the mass of the aluminum hydroxide, and the organic phosphinic acid is taken according to the mol ratio of the aluminum hydroxide to the organic phosphinic acid of 1/1.0 to 2.0; the aluminum hydroxide is dispersed in the organic solvent glacial acetic acid, the organic phosphinic acid is added into the aluminum hydroxide dispersing liquid during stirring, the reaction is carried out for 24 to 36h at the room temperature to 80 DEG C after the nitrogen gas is introduced for 10 to 30 minutes, and reacted materials are obtained; and the reacted materials are filtered while being hot, solid materials are washed and dried, and the phosphinic acid modified aluminum hydroxide flame retardant agents are prepared. When the method is adopted, the prepared phosphinic acid modified aluminum hydroxide flame retardant agents have better heat stability and hydrophobicity and are used in epoxy resin composite materials, the mechanical performance and the like of the composite materials are obviously improved, and the flame retardant performance is good.
Owner:SOUTHWEAT UNIV OF SCI & TECH

Method for producing lithium ion battery negative electrode material by asphalt secondary coating process

The invention proposes a method for producing a lithium ion battery negative electrode material by an asphalt secondary coating process. By the method, the problem that the electrochemical performanceof the lithium ion battery negative electrode material in the prior art is solved. The method comprises the following sequential steps of S1, mixing needle coke after being smashed and asphalt powderwith grain size being 20-40 micrometers for 20-30 minutes by a mixing machine to obtain a mixture A; S2, performing surface modification and fusion on the mixture A to obtain a primary asphalt coating material, allowing the primary asphalt coating material to enter a furnace for high-temperature graphitization at 800 DEG C under protection of high-pure N2, and cooling to a room temperature to obtain a material B; S3, smashing and classifying the material B, and mixing the material and asphalt powder with grain size being 2-5 micrometers again for 30-40 minutes by the mixing machine to obtaina material C; and S4, fusing the material C to obtain a secondary asphalt coating material, sending the secondary asphalt coating material to another one furnace for high-temperature carbonization at3,000 DEG C under protection of high-pure N2, and removing tar contained in the material C, thereby obtaining the lithium ion battery negative electrode material.
Owner:WEIFANG HUICHENG NEW MATERIAL TECH

Monolithic chromium oxide catalyst as well as preparation method and application thereof

The invention discloses a preparation method for a monolithic chromium oxide catalyst. The preparation method comprises the following steps: preparing a monolithic catalyst provided with a chromium oxide coating by adopting an impregnation method: weighing a chrome precursor and dissolving the chrome precursor in deionized water, stirring the solution at normal temperature, pouring the chrome precursor on a cordierite honeycomb ceramic carrier after the chrome precursor is dissolved uniformly, after the cordierite honeycomb ceramic carrier is impregnated repeatedly, drying at 100 DEG C, and roasting for 4 hours at 300 DEG C to obtain the monolithic catalyst provided with the chromium oxide coating; preparing the monolithic chromium oxide catalyst by an alkaline liquid processing method: soaking the monolithic catalyst provided with the chromium oxide coating prepared by the step (1) in an alkaline liquid in an excessive impregnating way, wherein the PH of the alkaline liquid is 8 to 10, soaking the monolithic catalyst provided with the chromium oxide coating, roasting the monolithic catalyst provided with the chromium oxide coating for 2 to 6 hours after being dried for 12 hours, thereby obtaining the alkaline liquid surface processed monolithic chromium oxide catalyst. The catalytic oxidation of a NO reaction at normal temperature is realized; NO can be eliminated at the normal temperature; the engineering application is realized. The catalyst disclosed by the invention has a good application prospect because raw materials are easily available and the process is simple.
Owner:SHANGHAI NAT ENG RES CENT FORNANOTECH

PLGA (Poly Lactic-co-Glycolic Acid)-gelatin composite microspheres carrying genistein and preparation method thereof

The invention discloses PLGA (Poly Lactic-co-Glycolic Acid)-gelatin composite microspheres carrying genistein and having a controlled-release effect and a preparation method thereof, and belongs to the technical field of biomedical materials. The method comprises the following steps: preparing gelatin nanoparticles by a two-step desolvation method; adsorbing the genistein in the gelatin nanoparticles; entrapping the gelatin nanoparticles adsorbing drugs in PLGA microspheres by an improved S / O / W method to prepare the PLGA-gelatin composite microspheres carrying the genistein, which have the advantages of high drug loading capacity, capability of overcoming burst release of drugs and uniform particle sizes and are applied in the field of drug delivery. The obtained PLGA-gelatin composite microspheres carrying the genistein are white or faint yellow in appearance, and are 3 to 8mu m in particle sizes, the particles are dispersed, and adhesion is prevented; the highest drug loading amount of the genistein is about 12.1 percent by weight. The gelatin nanoparticles prepared in a preparing process are 60 to 300 nanometers in particle sizes, drugs are released hardly within 24 hours, and the release rate of the genistein is about 80 percent within 20 days along with the degradation of the composite microspheres.
Owner:JILIN UNIV
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