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144results about How to "Good superparamagnetic" patented technology

Preparation method of magnetic iron-based heterogeneous Fenton catalyst taking graphene as carrier and application

The invention relates to a preparation method of a magnetic iron-based heterogeneous Fenton catalyst taking graphene as a carrier and an application. According to the method, the graphene serves as the carrier, magnetic nano-scale ferroferric oxide and nano-scale zero-valent iron (Fe0) are compounded to the surface of the graphene to serve as the heterogeneous Fenton catalyst in an in-situ growth mode, aggregation of catalytic active nano-particles can be effectively prevented by the graphene serving as the carrier, and more active sites are exposed. Besides, the graphene has high electron transfer capability, Fe0 easily transfers electrons to Fe3+ by taking the graphene as the carrier, Fe3+ is promoted to be transformed into Fe2+, so that catalytic activity of the catalyst is improved, the catalyst is easily recovered and reusable, pollutant removal efficiency is improved, phenol removal efficiency reaches 99% or more, and the used catalyst is recovered by an external magnetic field. The preparation method solves the problems that traditional Fenton catalysts are difficultly recycled and generate a lot of chemical sludge, and the preparation method has a certain economic value and practical value.
Owner:XINJIANG TECHN INST OF PHYSICS & CHEM CHINESE ACAD OF SCI

Preparation method for core-shell structure type carbon-coated magnetic nano particles

The invention discloses a preparation method for core-shell structure type carbon-coated magnetic nano particles. The method comprises the following steps: preparing metal hydroxide or metal oxide nano particles having different morphologies by adopting a hydrothermal method; modifying the surfaces of the particles; coating the nano particles by adopting a similar method (described in the specification) so as to obtain phenolic resin-coated metal oxide or metal hydroxide nano composite particles; and performing calcining and carbonizing on the obtained nano composite particles to obtain the carbon-coated magnetic nano particles. The carbon-coated magnetic nano particles prepared by adopting the method disclosed by the invention are good in dispersibility, uniform in particle size and high in stability, and have graded porous core-shell structures; in the calcining process, the morphologies of the core-shell metal hydroxide or metal oxide nano particles can be kept unchanged; the particle diameters of the nano particles and the coating thickness of a carbon layer can be adjusted according to needs. The core-shell structure type composite particles prepared by adopting the method disclosed by the invention have a superpara magnetism adsorption property, and under the action of an external magnetic field, the fast separation can be realized, so that the core-shell structure type composite particles can be expected to be applied in the fields of magnetic separation and catalyzing.
Owner:DONGHUA UNIV

Preparation and application of amino modified Fe3O4@SiO2@mSiO2 composite particles with mesoporous structure

InactiveCN105964216AGood superparamagneticImproved saturation magnetizationOther chemical processesWater contaminantsSorbentSilanes
The invention relates to a preparation method of amino modified Fe3O4@SiO2@mSiO2 composite particles with a mesoporous structure. The preparation method comprises the steps: dispersing Fe3O4@SiO2 powder into a mixture solution of ethanol, deionized water, ammonia water and a template agent, so as to obtain a sol solution; then, dropwise adding TEOS into the sol solution, so as to prepare Fe3O4@SiO2@mSiO2 composite particles with the mesoporous structure; drying the Fe3O4@SiO2@mSiO2 composite particles, then, adding ethylene glycol into the dried Fe3O4@SiO2@mSiO2 composite particles, carrying out ultrasonic separation, then, adding a silane reagent, carrying out high-temperature refluxing while carrying out stirring so as to enable the silane reagent to be adsorbed into mesoporous pore passages of SiO2, carrying out a hydrolytic reaction, removing unreacted silane reagent or the silane reagent which is not adsorbed into the mesoporous pore passages, and finally, carrying out vacuum drying, thereby obtaining the amino modified Fe3O4@SiO2@mSiO2. According to the preparation method, SiO2 with a mesoporous structure serves as a shell layer, a nanoparticle Fe3O4 serves as a magnetic core, the stability in an acidic solution system is excellent, the difficult problem of the ordinary adsorbents that the separation is difficult after adsorption can be solved, the efficiency of adsorbing a target product is increased, and the reuse rate of an adsorbent is increased, so that the preparation method has good economic and environmental benefits.
Owner:XI'AN UNIVERSITY OF ARCHITECTURE AND TECHNOLOGY

Surface-aminated Fe3O4 nano particle and preparation method and application thereof

The invention discloses a surface-aminated Fe3O4 nano particle and a preparation method and the application thereof. The method comprises the following steps: (1) in inert atmosphere, FeCl2 and FeCl3 are added into the mixed solution of sodium hydroxide aqueous solution and hydrochloric acid aqueous solution for reaction and Fe3O4 nano particles are obtained; (2) ethanol solution of the Fe3O4 nano particles is prepared; in inert atmosphere, strong ammonia water and tetraethoxysilane are added into the ethanol solution of the Fe3O4 nano particles and after reaction, modified Fe3O4 nano particles are obtained; and (3) the ethanol solution of the Fe3O4 nano particles with a good dispersion effect is prepared; in inert atmosphere, 3-aminopropyl triethoxy silane is added into the ethanol solution of the modified Fe3O4 nano particles and after reaction, the surface-aminated Fe3O4 nano particles are obtained. The aminated Fe3O4 nano particles provided by the invention can have good adsorption capacity to 5 types of phenylarsonic acid at the same time. At the same time, as the aminated Fe3O4 nano particles have superparamagnetism, centrifugalization is unnecessary for sample treatment. Thus, the steps of pretreatment of samples are greatly simplified, the pretreatment time is shortened and the efficiency of the pretreatment of samples is increased.
Owner:INST OF QUALITY STANDARD & TESTING TECH FOR AGRO PROD OF CAAS

High molecule liposome and uses thereof

The invention relates to a preparation and application of a new macromolecule lipidosome. The structure is a vesicle which has a lipide dual-layer structure containing duoparental chitosan longchain alkyl quaternary ammonium salt as well as phospholipid with micromolecule. The chitosan longchain alkyl quaternary ammonium salt is characterized in that: the weight average molar mass is bigger than 2000; the chitosan longchain alkyl quaternary ammonium salt can be dissolved in chloroform and other organic solvent, which contains carboxyl, amino or quaternary ammonium salt radical and concretely is one of the duoparental chitosan longchain alkyl quaternary ammonium salt disclosed by 200710056993.4 of China Invention Patent. The surface of the macromolecule lipidosome can be connected with various Liver-Targeted preparations. The macromolecule lipidosome can carry water-soluble, oil-dissolving or duoparental materials including medicine, protein, gene, nutrition, vitamin, magnetic granule and quantum dot, etc. The macromolecule lipidosome has the advantages of high wrapping rate, simple and convenient operation, strong applicability and low cost; the macromolecule lipidosome after being covered has even distributed granule diameter which can be lower than 20nm for the smallest, has stable system and strong functions for carrying medical tiny balls and slowly controlling as well as releasing.
Owner:TIANJIN UNIV

Nanometer ferroferric oxide core-carbon meso pore hollow shell complex, as well as preparation method and application thereof

The invention discloses a nanometer ferroferric oxide core-carbon meso pore hollow shell complex, as well as a preparation method and application thereof. The complex is formed by ferroferric oxide particles and a carbon shell sleeved and sealed outside, wherein the carbon sheel is of a mesoporous structure with the hole diameter being 1-5nm; the grain size of the ferroferric oxide particles is 8-12nm; the external diameter of a carbon mesoporous shell is 80-100nm; the thickness of the shell is 10-20nm; and the diameter of a hollow part between the ferroferric oxide and the carbon mesoporous shell is 30-60nm. The preparation method comprises the following steps of: synthetizing ferroferric oxide nanometer nanometers through a high-temperature reflux method, using a microemulsion method to obtain a ferroferric oxide core silicon dioxide shell powder body; then depositing a layer of mesoporous silicon dioxide on the surface of a silicon dioxide shell through a chemical method to obtain a three-layer core shell structure; taking the three-layer core shell structure as a hard template, and depositing carbon in clearances of the mesoporous silicon dioxide; and finally, etching the silicon dioxide by utilizing strong alkali solution, thereby obtaining a target product. The nanometer ferroferric oxide core-carbon meso pore hollow shell complex can be used for carrying out adsorption processing in solution polluted by methylthionine chloride, congo red or phenol.
Owner:HEFEI INSTITUTES OF PHYSICAL SCIENCE - CHINESE ACAD OF SCI

Novel mesoporous silicon sphere co-loaded medicine nano-complex and preparation method thereof

The invention discloses a novel mesoporous silicon sphere co-loaded medicine nano-complex and a preparation method thereof. The novel mesoporous silicon sphere co-loaded medicine nano-complex is Ce6@MMSN / DOX / Ko143@PAsp-b-PEG-FA; the preparation method comprises the following steps: selecting TEOS (Tetraethyl Orthosilicate) as a silicon source, CTAB (Cetyltrimethyl Ammonium Bromide) as a template agent and n-hexane as a pore expanding agent and synthesizing mesoporous silicon dioxide nanoparticles with a double-pore-channel core-shell structure; carrying out amination modification on the mesoporous silicon dioxide nanoparticles; synthesizing Fe3O4 nanoparticles by adopting an LSS (Liquid-Solid-Solution) phase transfer method and ligand exchange reaction; modifying and embedding superparamagnetic iron oxide nanoparticles on the surface of aminated MSN through nucleophilic substitution, so as to construct magnetic mesoporous silicon dioxide nanoparticles; taking DCC (Dicyclollexyl Carbodiimide) as a condensation agent and covalently binding a photosensitizer Ce6 through amidation; meanwhile, loading a BCRP (Breast Cancer Resistance Protein) inhibitor Ko143; then crossly linking a copolymer FA-PEG-b-PAsp; finally, loading an anti-tumor medicine DOX.
Owner:SECOND AFFILIATED HOSPITAL SECOND MILITARY MEDICAL UNIV

Preparation method for magnetic carbon nanotube demulsifier and application of magnetic carbon nanotube demulsifier

The invention discloses a preparation method for a magnetic carbon nanotube demulsifier. The preparation method comprises the following steps: (1) subjecting carbon nanotubes and mixed acid to a refluxing reaction, so as to obtain oxidation modified carbon nanotubes; (2) preparing a Fe3O4 precursor solution; and (3) uniformly mixing the oxidation modified carbon nanotubes with the Fe3O4 precursorsolution, and carrying out a reaction at a temperature of 180 DEG C to 220 DEG C, thereby preparing the magnetic carbon nanotube demulsifier. According to the preparation method provided by the invention, firstly, the carbon nanotubes are subjected to oxidation modification through the mixed acid to introduce a large number of carboxyl groups and hydroxyl groups to defects and edges of the carbonnanotubes, and then, Fe3O4 nanoparticles are prepared in situ by utilizing a hydrothermal method to modify the oxidation modified carbon nanotubes; the preparation method is simple and is easy to implement; and the prepared magnetic carbon nanotube demulsifier can be used for rapidly achieving oil-water separation of oily wastewater and is relatively good in demulsification effect. A technical scheme of the invention further provides an application of the magnetic carbon nanotube demulsifier in the oily wastewater.
Owner:新疆澄润环保科技有限公司

Magnetic nano mixed semi micelle and preparation method thereof as well as application of magnetic nano mixed semi micelle in adsorbing and separating cationic dye from environmental water sample

The invention provides a magnetic nano mixed semi micelle and a preparation method thereof as well as an application of the magnetic nano mixed semi micelle in adsorbing and separating a cationic dye from an environmental water sample. The magnetic nano mixed semi micelle consists of a carrier and a surface micelle layer, wherein the carrier is magnetic nano particles, the surface of the carrier is a mixed semi micelle formed by an anionic surface active agent; the magnetic nano particles are Fe3O4 or gamma-Fe2O3; and the anionic surface active agent is sodium dodecyl sulfate, sodium dodecylbenzene sulfonate or sodium n-alkyl benzene sulfonate. The magnetic nano mixed semi micelle prepared by the method provided by the invention not only has the advantages of large specific area and high adsorption capacity of a nano material, but also has good magnetic separating power of a magnetic material; when the magnetic nano mixed semi micelle is applied to solid phase extraction, the adsorption time can be greatly shortened; and the preparation method of the adsorbent is simple, low in cost and very suitable for large-scale batch processing of the environmental water sample.
Owner:SOUTH CHINA UNIV OF TECH

Preparation method of CD133 immunomagnetic beads

The invention discloses a preparation method of CD133 immunomagnetic beads. The preparation method comprises the following steps: preparing magnetic beads; preparing magnetic chitosan microspheres; weighing 10 g of chitosan, and adding the weighed chitosan into 200 ml of a 2% acetic acid solution for overnight soaking to enable dissolution; adding 1 g of Fe2O4 nano magnetic beads into the mixed solution, and performing stirring at the room temperature under the condition of 300 r/min; adding 200 ml of saxoline, and performing stirring at 40 DEG C under the condition of 300 r/min; raising the temperature to 50 DEG C, adding 40 ml of formaldehyde, and performing stirring under the condition of 300 r/min; adding 20 ml of glutaraldehyde with the volume concentration of 50% into the mixed solution, performing stirring at 60 DEG C under the condition of 170 r/min, adjusting the pH to be 10, and performing stirring for 2-6 h; adding 100 ml of petroleum ether into a reaction system after finish of reaction, fully performing stirring, performing suction filtration by use of a Buchner funnel to obtain magnetic chitosan microsphere particles, then fully performing stirring and washing by use of ethyl alcohol, washing with distilled water after removal of ethyl alcohol, and performing vacuum drying at 50 DEG C; performing carboxylation on the magnetic chitosan microspheres; and coupling immunomagnetic beads subjected to carboxylation with an anti-body. The preparation method has the advantages of good stability, high sensitivity and the like.
Owner:安徽安龙基因科技有限公司

Method for preparing magnetic gene-loaded lipid ultrasonic microbubble contrast medium

The invention discloses a method for preparing magnetic lipid ultrasonic microbubble contrast medium. The method comprises the following steps: preparing FeCl3 and FeCl2 solution and adding the solutions into a flask; dripping NH4OH under stirring condition so as to generate precipitation and curing; taking out and flushing the generated product until the pH value is 7; drying generated product to obtain the Fe3O4 magnetic nano particles; preparing the Fe3O4 dry powder into magnetic fluid; discarding the supernatant, suspending precipitation again in phosphate buffer and adding PEI to form PEI / Fe3O4 nano particles; mixing the PEI / Fe3O4 nano particles with pEGFP-C1 plasmid DNA for standing to obtain gene-loaded Fe3O4 magnetic nano particles; dissolving DSPC, DPPE and DPPA in an organic solvent in which the ratio of chloroform to isopropanol is 2:1; evaporating the solvent to leave a lipid film; preparing hydration solution from glucose and propylene glycol in a ratio of 4:1 and adding the hydration solution into the flask, and dispersing the hydration solution to obtain lipid suspension; adding 40 mg of PEG4000, heating the mixed suspension for dissolving; adding DNA / PEI / Fe3O4 and gelatin into the lipid suspension; adding 800.01 ml of Tween; replacing air above a penicillin bottle; and shaking the suspension to obtain the gene-loaded magnetic lipid ultrasonic microbubbles.
Owner:SOUTHEAST UNIV
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