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34results about How to "Adjustable specific surface area" patented technology

Continuous cellulose aerogel fiber and preparation method thereof

The invention provides a continuous cellulose aerogel fiber and a preparation method thereof. The preparation method comprises the following steps: dispersing cellulose into a dispersing agent so as to obtain a spinning stock solution; extruding the spinning stock solution into a coagulating bath for wet-method spinning so as to obtain cellulose aerogel fiber; winding the cellulose aerogel fiber in the coagulating bath, and soaking into an aging liquid for aging; washing the aged cellulose aerogel fiber till the pH is neutral, and drying, so as to obtain the continuous cellulose aerogel fiber. The preparation method provided by the invention has the characteristics that raw materials are cheap and easy to obtain, the preparation process is simple, green and pollution-free, the continuous cellulose aerogel fiber is good is spinnability, and the problem that cellulose aerogel is hard to spin into fiber is solved. The diameter of the cellulose aerogel fiber provided by the invention is smaller than 120 [mu]m, the cellulose aerogel fiber has the characteristics of high specific surface area (greater than or equal to 88m<2>/g), high porosity (greater than or equal to 85%), and low density (less than or equal to 0.2/cm<3>), meanwhile the fiber specific surface area can be adjusted, and the cellulose aerogel fiber can be used in fields such as functional clothes, sensing, catalyst loading and adsorption filtration, cosmetics and biological treatment.
Owner:DONGHUA UNIV

Preparation method of resin used for blood purification to remove β2-microglobulin

The invention discloses a preparing method for resin for clearing away beta2-microglobulin in blood purification. The preparing method comprises the steps that firstly, polystyrene-divinylbenzene microspheres are prepared; secondly, the polystyrene-divinylbenzene microspheres and chloromethyl ether are subjected to a chloromethylation reaction, and chloromethylation microspheres are obtained; finally, long-chain hydrophobic groups are grafted to the chloromethylation microspheres. By means of the preparing method, styrene and divinybenzene serve as monomers, the polystyrene-divinylbenzene microspheres are obtained through suspension polymerization, and the size of pores in the microspheres is adjusted with a certain quantity of a pore-forming agent in the synthesizing process; then the microspheres serve as a carrier, alkyl is grafted through the chloromethylation reaction and an amination reaction, the microspheres with the adjustable specific surface area and the hydrophobic groups are obtained, and the resin is smooth in surface and high in strength and has very high adsorption performance on beta2-microglobulin in a uremia patient. The production technology is simple, the yield is high, and the product purity is high; meanwhile, raw materials are easy to obtain, and mass production and preparation can be achieved.
Owner:重庆希尔康血液净化器材研发有限公司

Submillimeter-level polystyrene-base spherical active carbon, and preparation method and application thereof

The invention discloses a submillimeter-level polystyrene-base spherical active carbon, and a preparation method and application thereof. The preparation method comprises the following steps: preparing polystyrene-base microspheres from styrene and divinylbenzene, swelling the polystyrene-base microspheres in carbon tetrachloride, adding a catalyst, and curing to form to obtain the super-crosslinked thermosetting polystyrene-base resin spheres; immersing the resin spheres in a saturated sodium chloride solution, cleaning sequentially with dilute hydrochloric acid, a sodium hydroxide solution and deionized water to a neutral state, and drying; carrying out high temperature carbonization and vapor activation to obtain polystyrene-base spherical active carbon; and carrying out surface modification on the polystyrene-base spherical active carbon by air oxidation and high-temperature nitrogen heat treatment. The preparation method is simple in technique, and lowers the production cost. The obtained spherical active carbon has the advantages of smooth surface, high sphericity and large specific area (up to 960-1400 m<2> / g), can be used for adsorbing urotoxin creatinine, and has wide application prospects in the field of uremia treatment.
Owner:CHANGZHOU YINGZHONG NANO TECH

A kind of preparation method of continuous sio2 airgel fiber

ActiveCN105671687BAdjust the size of the specific surface areaInnovativeInorganic material artificial filamentsWet spinning methodsFiberSilicic acid
The invention relates to a preparation method of continuous SiO2 aerogel fibers. The method comprises the following steps: processing silicate or silanol sol to prepare a spinning stock solution; adding an acidic solution to a coagulation tank to form a coagulation bath; and injecting the spinning stock solution to the coagulation bath, carrying out reaction wet spinning to obtain orthosilicic acid / silicate fibers, reeling the orthosilicic acid / silicate fibers, immersing the reeled fibers in an ageing solution, ageing the immersed fibers at normal temperature for 2-10d, washing the aged fibers with deionized water until the aged fibers are neutral, carrying out solvent displacement, and drying the obtained fibers to obtain the continuous SiO2 aerogel fibers. The method has the characteristics of cheap and easily available raw materials, simple reaction process and good spinnability, and solves the problem of difficult production of fibers through spinning SiO2 aerogel. The inorganic SiO2 aerogel fibers prepared in the invention have the characteristics of abundant holes, high specific surface area, high temperature resistance, chemical corrosion resistance and adjustable specific surface area, and can be applied in the fields of catalyst carriers and adsorbing filtration.
Owner:DONGHUA UNIV

Method for preparing basic nickel silicate catalyst from silicon-containing industrial solid waste

The invention discloses a method for preparing a basic nickel silicate catalyst from silicon-containing industrial solid waste, and belongs to the technical field of solid waste resource utilization.Pretreated silicon-containing industrial solid waste is adopted as a silicon source, a silicon-based precursor and a nickel-based precursor are added at the same time, three-dimensional basic nickel silicate is synthesized in a one-step hydrothermal mode, and the defect that a step-by-step synthesis method is tedious in step is overcome. Silicon-containing industrial solid waste is adopted as a silicon source, the nickel silicate material is prepared through a one-step hydrothermal method, the process is simple, operation is easy and convenient, the preparation period is short, and a special reaction container is not needed. The used raw materials are relatively low in cost, high-valued utilization of wastes is realized, and the method is suitable for batch production. The basic nickel silicate catalyst obtained by the invention has the advantages of high specific surface area, high mechanical strength, high activity, high stability, good thermal stability and low cost, and is suitablefor high-temperature catalytic reaction after reduction.
Owner:SHANDONG UNIV OF SCI & TECH

Method for producing capillary electrochromatography monolithic column made from silicon dioxide-titanic oxide integral material and uses thereof

The invention discloses a method for preparing an electrochromatography monolithic column of silicon dioxide-titanium dioxide monolithic materials, as well as application thereof. The titanium dioxide-silicon dioxide forms a mesopore molecular sieve under the action of a supramolecular template of which the mechanical strength is good, and pore diameter is easy to control according to requirement. A uniform capillary electrochromatography column with high specific surface area is prepared by one-step method. The method has the advantages that the mesopore molecular sieve which is prepared by using the supramolecular template as a structure-directing agent and has a specific pore structure, extremely high specific surface area and uniform adjustable pore diameter has the advantages of simple preparation method, good repeatability and high separation efficiency, and is suitable for the separation and enrichment of phosphorylated polypeptide, wherein titanium dioxide and silicon dioxide molecules are combined with silicon hydroxyl on the surface of the inner wall of a capillary through chemical bonds; a framework structure and the pore diameter of nanometer pores can be conveniently controlled by changing the categories and proportion of the supramolecular template; and surface properties and the chemical environment of a pore cavity are regulated so as to provide a specific molecular field.
Owner:EAST CHINA UNIV OF SCI & TECH

Lignin-based hierarchical porous carbon for rapidly purifying dye wastewater and preparation method of lignin-based hierarchical porous carbon

The invention belongs to the technical field of effective utilization of low-value and waste biomass resources, and particularly discloses lignin-based hierarchical porous carbon for rapidly purifying dye wastewater and a preparation method of the lignin-based hierarchical porous carbon. The preparation method comprises the following steps: (1) dissolving lignin in a potassium hydroxide solution, uniformly conducting stirring, and conducting evaporating and concentrating to obtain a pasty thick potassium hydroxide / lignin mixture; (2) performing high-temperature carbonization and activation on the concentrated potassium hydroxide / lignin mixture in the step (1) in a nitrogen atmosphere to obtain a black carbon solid; and (3) conducting deacidification treatment, namely neutralizing the black carbon solid obtained in the step (2) with diluted hydrochloric acid, conducting washing with water until the black carbon solid is neutral, and conducting drying to obtain the lignin-based hierarchical porous carbon. The lignin-based hierarchical porous carbon prepared by the method disclosed by the invention has relatively high adsorption capacity and rapid removal capacity on anionic dyes and cationic dyes, and can realize rapid, efficient and universal adsorption of organic dyes in a water body.
Owner:SOUTH CHINA UNIV OF TECH

Method for preparing high-specific-surface-area continuous SiO2 porous fiber through natural drying method

The invention relates to a method for preparing high-specific-surface-area continuous SiO2 porous fiber through a natural drying method. The method includes the steps of preparing a spinning solution from silicate or silanol sol, adding the spinning solution to an acid solution coagulating bath, conducting reaction and wet spinning to obtain orthosilicic acid/silicate fiber, winding the orthosilicic acid/silicate fiber, ageing the orthosilicic acid/silicate fiber at the normal temperature, washing the orthosilicic acid/silicate fiber with deionized water to be neutral, conducting solvent replacement through ethyl alcohol, and conducting natural drying. The method has the advantages that devices are simple, raw materials are low in price and easy to obtain, the reaction process is simple and spinnability is good, the problem that inorganic porous fiber can hardly be spun into fiber is solved, and meanwhile drying of the porous fiber is achieved through natural drying. The prepared SiO2 porous fiber has abundant pores, an ultrahigh specific surface area, high temperature resistance and chemical corrosion resistance, the specific surface area of the fiber can be adjusted, and the method can be used for the fields of catalyst carriers, adsorption filtration and the like.
Owner:DONGHUA UNIV

Method for preparing continuous hollow SiO2 porous fibers through non-coaxial spinning

The invention relates to a method for preparing continuous hollow SiO2 porous fibers through non-coaxial spinning. The method comprises steps as follows: a spinning solution is prepared from silicate; a strong acid solution is added to a coagulating basin to serve as a coagulating bath; the spinning solution is put in the coagulating bath, has a reaction and performs wet spinning, hollow orthosilicic acid/silicate fibers are obtained and subjected to winding, and the fibers after winding are immersed in an ageing solution for ageing; the fibers are washed to be neutral with deionized water after ageing, solutions in the fibers are replaced through ethanol, the fibers are dried, and the continuous hollow SiO2 porous fibers are obtained. According to the method, equipment is simple, raw materials are cheap and easy to obtain, the reaction process is simple, and the spinnability is good. The hollow inorganic SiO2 porous fibers prepared with the method have rich pores, ultrahigh specific surface area and high temperature resistance and chemical corrosion resistance, meanwhile, the specific surface area of the fibers can be adjusted, and the continuous hollow SiO2 porous fibers have more advantages in the fields such as catalysis, adsorption, filtration and the like than ordinary porous fibers.
Owner:DONGHUA UNIV

A kind of continuous cellulose airgel fiber and its preparation method

The invention provides a continuous cellulose aerogel fiber and a preparation method thereof. The preparation method comprises the following steps: dispersing cellulose into a dispersing agent so as to obtain a spinning stock solution; extruding the spinning stock solution into a coagulating bath for wet-method spinning so as to obtain cellulose aerogel fiber; winding the cellulose aerogel fiber in the coagulating bath, and soaking into an aging liquid for aging; washing the aged cellulose aerogel fiber till the pH is neutral, and drying, so as to obtain the continuous cellulose aerogel fiber. The preparation method provided by the invention has the characteristics that raw materials are cheap and easy to obtain, the preparation process is simple, green and pollution-free, the continuous cellulose aerogel fiber is good is spinnability, and the problem that cellulose aerogel is hard to spin into fiber is solved. The diameter of the cellulose aerogel fiber provided by the invention is smaller than 120 [mu]m, the cellulose aerogel fiber has the characteristics of high specific surface area (greater than or equal to 88m<2> / g), high porosity (greater than or equal to 85%), and low density (less than or equal to 0.2 / cm<3>), meanwhile the fiber specific surface area can be adjusted, and the cellulose aerogel fiber can be used in fields such as functional clothes, sensing, catalyst loading and adsorption filtration, cosmetics and biological treatment.
Owner:DONGHUA UNIV

A kind of submillimeter polystyrene-based spherical activated carbon and its preparation method and application

The invention discloses a submillimeter-level polystyrene-base spherical active carbon, and a preparation method and application thereof. The preparation method comprises the following steps: preparing polystyrene-base microspheres from styrene and divinylbenzene, swelling the polystyrene-base microspheres in carbon tetrachloride, adding a catalyst, and curing to form to obtain the super-crosslinked thermosetting polystyrene-base resin spheres; immersing the resin spheres in a saturated sodium chloride solution, cleaning sequentially with dilute hydrochloric acid, a sodium hydroxide solution and deionized water to a neutral state, and drying; carrying out high temperature carbonization and vapor activation to obtain polystyrene-base spherical active carbon; and carrying out surface modification on the polystyrene-base spherical active carbon by air oxidation and high-temperature nitrogen heat treatment. The preparation method is simple in technique, and lowers the production cost. The obtained spherical active carbon has the advantages of smooth surface, high sphericity and large specific area (up to 960-1400 m<2> / g), can be used for adsorbing urotoxin creatinine, and has wide application prospects in the field of uremia treatment.
Owner:CHANGZHOU YINGZHONG NANO TECH

Preparation method of in situ c-sio2 composite coating on the surface of continuous sic fiber

The invention provides a method for preparing a surface in-situ C-SiO2 composite coating of continuous SiC fibers and relates to continuous SiC fibers. The method comprises the steps: placing SiC fibers in a muffle furnace, carrying out heating in an air atmosphere, and then, carrying out furnace cooling until the temperature is room temperature in the air atmosphere, so as to obtain a degummed SiC fiber sample A; placing the degummed SiC fiber sample A in a porous graphite boat, placing the graphite boat in a heating-up tubular furnace, introducing an inert atmosphere at room temperature, andexhausting air in the tubular furnace; heating the obtained degummed SiC fiber sample A under the protection of an inert atmosphere, then, closing a N2 gas valve, opening a Cl2 gas valve, adjusting chlorine gas flow-rate, carrying out heat preservation, forming the C-SiO2 composite coating on the surface of the SiC fibers in situ through regulating and controlling a process, carrying out heat preservation, then, closing Cl2 gas, and carrying out furnace cooling until the temperature is room temperature under the protection of an inert atmosphere, thereby obtaining the surface in-situ C-SiO2 composite coating of the continuous SiC fibers.
Owner:XIAMEN UNIV

A method for preparing continuous SiO2 porous fibers with high specific surface area by natural drying method

ActiveCN105603578BAdjust the size of the specific surface areaSolve the difficult problem of spinning into fiberInorganic material artificial filamentsPolymer scienceAlcohol
The invention relates to a method for preparing high-specific-surface-area continuous SiO2 porous fiber through a natural drying method. The method includes the steps of preparing a spinning solution from silicate or silanol sol, adding the spinning solution to an acid solution coagulating bath, conducting reaction and wet spinning to obtain orthosilicic acid / silicate fiber, winding the orthosilicic acid / silicate fiber, ageing the orthosilicic acid / silicate fiber at the normal temperature, washing the orthosilicic acid / silicate fiber with deionized water to be neutral, conducting solvent replacement through ethyl alcohol, and conducting natural drying. The method has the advantages that devices are simple, raw materials are low in price and easy to obtain, the reaction process is simple and spinnability is good, the problem that inorganic porous fiber can hardly be spun into fiber is solved, and meanwhile drying of the porous fiber is achieved through natural drying. The prepared SiO2 porous fiber has abundant pores, an ultrahigh specific surface area, high temperature resistance and chemical corrosion resistance, the specific surface area of the fiber can be adjusted, and the method can be used for the fields of catalyst carriers, adsorption filtration and the like.
Owner:DONGHUA UNIV
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