105results about How to "Uniform pores" patented technology

The present invention provides for a multi-composite adsorbent mixture which will remove H2O, CO2 and nitrogen oxides and/or hydrocarbons from a feed gas stream. The improvement lies in the use of a third adsorbent which is selective for nitrogen oxides, hydrocarbons or both.

The invention discloses a preparation method of ordered mesoporous titania/silver photocatalyst, relating to a preparation method of titania/silver and aiming to solve the technical problems of small specific surface area, poor orderliness and low photocatalytic activity of mesoporous titania/silver photocatalyst prepared by prior arts. The preparation method comprises the steps of silver solution preparation, titanium precursor preparation, titania/silver gel preparation, and heat treatment. The inventive photocatalyst has specific surface area of 120-160 m<2>/g, has the advantages of uniform mesopores and high catalytic activity; can be applied to photocatalysis field, and water treatment field of lake, ocean, municipal sewage and industrial sewage.

Disclosed are mesoporous silica particles and a preparation method thereof, particularly, a method of preparing mesoporous silica particles, including mixing a silica precursor, an alkylamine-based surfactant, and a phosphoric acid-based cosurfactant, thus preparing a mixture solution (a mother liquor); adding or not adding the mixture solution with an acid solution, and conducting stirring, thus providing mesoporous silica particles; and thermally treating the mesoporous silica particles. These mesoporous silica particles are prepared using a phosphoric acid-based cosurfactant for stabilizing the surface of the particles to prevent the aggregation thereof, thereby uniformly distributing the particles. Through a hydrothermal reaction, the mesoporous silica particles have various pore sizes, a large surface area, and a high pore volume, and thus are widely used in catalysts, adsorbents, low dielectrics, and separation and purification processes, and are useful as templates for the preparation of novel porous materials, including porous carbon.

The present invention provides a silicon carbide-based heat-resistant, ultra lightweight, porous structural material having the same shape as that of a spongy porous body and also provides a process for readily producing the material. In the process of the present invention, slurry containing silicon powder and a resin is applied to the framework of the spongy porous body by an impregnation method in such a manner that interconnected pores of the porous body are not plugged with the slurry; the resulting porous body is carbonized at a temperature of 900° C. to 1320° C. in vacuum or in an inert atmosphere; the resulting porous body is subjected to reactive sintering at a temperature of 1320° C. or more in vacuum or in an inert atmosphere, whereby silicon carbide having high wettability to molten silicon is produced and open pores due to a volume reduction reaction are formed in one step; and molten silicon is infiltrated into the resulting porous body at a temperature of 1300° C. to 1800° C. in vacuum or in an inert atmosphere, whereby the silicon carbide-based heat-resistant, ultra-lightweight, porous structural material is produced.

In the invention, with being fixed in macropore-micropore multistage ordered zeolite structure through the ion exchnage process, the transition metal ions are as the affiliation active spots where the distinctive combination is occurred with the functional biomacromolecules possesisng the sequential histidine structure. Then, using the gradient elution through the buffer solution to reach the goal of enrich and separation. The carrier provides the advantages of even pore passages, good mechanical and chemical stability, easy to modify the surfaces etc. The diatomaceous earth is as the moldingboard and the molecular sieve of nano Beta zeolite wit surface being modified is as affinity chromatography filler. With the column being filled with the said materials, the satisfying result for separating the functional protein molecules is obtained in different leaching systems.

The invention discloses a preparation method of a polyvinylidene fluoride hollow fiber micropore filter membrane. The preparation method includes the steps of: preparing a film casting liquid; preparing a core liquid; preparing an outer solidifying liquid; performing spinning; performing rinsing replacement; and performing thermal treatment. The method is used for preparing the PVDF hollow fiber micropore filter membrane through combination of thermally induced phase separation and solution phase conversion; compared with the solution phase conversion method, finger-like holes are eliminated, and the microstructure of the membrane is more reasonable; and compared with the thermally induced phase separation method, the method simplifies operations, is free of solvent extraction and reduces cost; in the film casting liquid, inorganic additives, such as nano glass powder or nano silicon carbide, are added, so that strength of membrane filaments is enhanced, and especially, pressure resistance and wear resistance of the membrane filaments are improved. The method can be used for preparing internal-pressure or external-pressure membrane filaments having a skin layer. The microstructure under the skin layer is also in a network structure or a particle stacking structure. The membrane filaments have good separation performance and high flux.

A microwave integrated machine for production of an aerogel material and a method for continuous production of the aerogel material are disclosed. The invention belongs to the technical field of aerogel material production and especially relates to a microwave integrated machine and an efficient production method for continuous production of the aerogel material by using the microwave technique. The invention aims to solve the technical problem that existing aerogel preparation methods have long production period and the internal skeleton structure is collapsed and the thermal insulation performance is reduced. The method of the invention comprises the following steps: preparing a wet aerogel material, letting the wet aerogel material enter a solvent replacement device and then enter a hydrophobic modification device, and drying to obtain the aerogel material; letting the evaporated solvent gas enter a shell and tube condenser, condensing for gas-liquid separation, recycling the solvent, returning an inert gas to the equipment for recycling so as to complete a production period. According to the method, each solvent replacement only takes more than ten minutes, and each hydrophobicmodification only takes more than ten minutes. Thereby, production efficiency is greatly improved.

The invention provides a porous oxide and a preparation method thereof. The preparation method comprises the following steps of mixing an inorganic salt solution with a polymer solution, so as to obtain a precursor solution; carrying out freezing treatment and drying treatment on the precursor solution in sequence, so as to obtain a porous-structure predecessor; carrying out calcination on the porous-structure predecessor, so as to obtain the porous oxide. According to the preparation method, through the assistance of a polymer, the polymer is closely combined with an inorganic salt together; the growth of an ice crystal is impeded; a porous precursor is formed; the polymer is removed in a high-temperature calcination process; the inorganic salt is decomposed into an oxide and grows by using the porous precursor as a template, so as to obtain a porous oxide material which has a macroscopic three-dimensional structural feature and is uniform in pore canal.

Disclosed herein are an electrode paste for a solid oxide fuel cell in an anode supported type in which an anode, an electrolyte layer, and a cathode are sequentially stacked, including a raw material powder, a dispersant, a binder, a solvent, and a liquid pore-forming material, a solid oxide fuel cell using the same, and a fabricating method thereof. The electrode paste for the solid oxide fuel cell may form uniform pores in the electrode and may provide high porosity.

The invention discloses mesoporous ruthenium nanoparticles for targeted therapy of the colorectal cancer as well as a preparation method and application of the mesoporous ruthenium nanoparticles. Thepreparation method comprises the following steps: (1), dissolving ruthenium trichloride in a perchloric acid solution, then adding a nonionic surfactant, and mixing uniformly to obtain a mixed solution I; (2), adding amino-modified colloidal silicon dioxide nanoparticles into the mixed solution I, and ultrasonically mixing to obtain a uniform mixed solution II; (3), adding a sodium borohydride solution into the mixed solution II, performing an ultrasonic reaction, and after completion of the reaction, washing by using water and centrifuging to obtain an intermediate product; (4), dispersing the intermediate product in a hydrofluoric acid solution, then washing by using water and drying to obtain the mesoporous ruthenium nanoparticles for the targeted therapy of the colorectal cancer. The ruthenium nanoparticles prepared according to the preparation method provided by the invention have large specific surface area, can be loaded with a ruthenium complex and a coupled bispecific antibodyand are applied to targeted resistance to the colorectal cancer in combination with photothermal and immunotherapy.

The invention provides a preparation method of a microcapsule antibacterial functional finishing agent. According to the microcapsule antibacterial functional finishing agent, mesoporous silica coatedwith polyurethane serves as a wall material, aloin, lemon essential oil, vanilla oil and Chinese mugwort oil serve as core materials, and the weight ratio of the wall material to the core materials is 1:(1-5). A fabric finished by the finishing agent has good antibacterial effect, a combination action of the finishing agent and the fabric is high, and the antibacterial effect is more durable through sustained-release effect of a microcapsule. Antibacterial components used by the finishing agent are provided with natural extracts, safe and free from toxicity, and good health states of skins can be kept. The finishing agent has important application values in the field of textile.

The invention belongs to thel field of magnetic composite material synthesis technology, and particularly discloses a preparation method of a magnetic ordered mesopore Fe3O4@MCM-48 composite adsorbingmaterial. The preparation method includes steps of combining a ferrite Fe3O4 grain and a mesoporous molecular sieve MCM-48; roasting in a muffle furnace at 450-650 DEG C, so as to obtain the Fe3O4@MCM-48 magnetic mesopore composite adsorbing material with a core-shell structure. The method is low in cost, low in toxicity, simple in operation, gentle in condition, and short in consumed time; the prepared material has magnetism and the mesoporous duct of the molecular sieve; the preparation method has huge prospect in absorption and separation, and drug carrier.

The invention discloses a medium/low temperature mesoporous nitrogen oxide and dioxin removal catalyst and a preparation method thereof. According to the catalyst, a mesoporous carbon-silicon composite material is adopted as a carrier, and one or more of vanadium pentoxide, tungsten oxide, cerium oxide and manganese oxide are adopted as active components. The catalyst disclosed by the invention iscapable of effectively achieving synergetic removal of NOx and dioxin within a medium/low temperature range of 180-300 DEG C, and in addition, the catalyst disclosed by the invention has the advantages of being large in specific surface area, ordered in pore height, small in active metal particle size and uniform in active metal particle size distribution.

The invention provides a cadmium selenide quantum dot and nanoporous carbon composite material and a preparation method therefor. The cadmium selenide quantum dot and nanoporous carbon composite material is formed by cadmium selenide quantum dots and nanoporous carbon in a compounding manner; the cadmium selenide quantum dots are grown on the surface of the nanoporous carbon in an in-situ manner; and the nanoporous carbon is obtained by calcining a zeolite imidazate type coordination polymer under protection of an inert gas. The nanoporous carbon disclosed by the invention has the advantages of large specific surface area, uniform pore channels, and large pore channel dimensions; and when the composite material is formed by the nanoporous carbon and the cadmium selenide quantum dots, the dispersity of the cadmium selenide quantum dots can be improved, the crystal particle dimensions of the cadmium selenide quantum dots can be controlled, and generation of small-dimensional cadmium selenide quantum dots can be reduced, so that the photocatalytic efficiency and the service life of the composite material are obviously improved and prolonged.

The invention discloses a preparation method of a reinforced polyvinylidene fluoride hollow fiber micropore filter membrane. The preparation method includes the steps of: preparing a film casting liquid; preparing a support body; preparing an outer solidifying liquid; performing spinning; performing rinsing replacement; and performing thermal treatment. The method is used for preparing the PVDF hollow fiber micropore filter membrane through combination of thermally induced phase separation and solution phase conversion; compared with the solution phase conversion method, finger-like holes are eliminated, and the microstructure of the membrane is more reasonable; and compared with the thermally induced phase separation method, the method simplifies operations, is free of solvent extraction and reduces cost; in the film casting liquid, inorganic additives, such as nano glass powder or nano silicon carbide, are added, so that strength of membrane filaments is enhanced, and especially, pressure resistance and wear resistance of the membrane filaments are improved.

The invention relates to a high carrying capacity metal chelating affinity chromatography medium. Silica gel microspheres are adopted as a core; pores are formed inside the silica gel microspheres; carboxymethyl chitosan oligosaccharide molecules are adhered to the surfaces and the pores of the silica gel microspheres; a part of the carboxymethyl chitosan oligosaccharide molecules are complexed with first metal ions to form a first layer of metal chelating; the rest part of the carboxymethyl chitosan oligosaccharide molecules are bonded with allyl glycidyl ether; the allyl glycidyl ether is connected with aglycone; and the aglycone is complexed with second metal ions to form a second layer of metal chelating. By adopting the medium, double metal layers are successfully immobilized on the surface of the medium, the carrying capacity of the metal affinity chromatography medium is effectively increased, and the medium is simple in improvement method, low in production cost and beneficialto large-scale popularization and application.

The invention discloses a preparation method of a mesoporous lithium vanadium phosphate cathode material. The method comprises the following steps: (1) preparing a mixed solution from a vanadium source, a phosphorus source, a template agent and oxalic acid according to a ratio, and drying the mixed solution to obtain a dried mixture; (2) calcining the dried mixture obtained in the step (1) under inert atmosphere, then adding an alkaline solution and removing the template agent, washing and drying to obtain mesoporous vanadium phosphate; and (3) mixing mesoporous vanadium phosphate obtained inthe step (2) with a lithium source according to a mass ratio of 1 to (0.1-5), then adding the mixture to deionized water to prepare a solution with a lithium ion concentration of 0.01-10mol/L, duringand calcining under inert atmosphere, then removing unreacted lithium elements by using deionized water, and drying the solution to obtain mesoporous lithium vanadium phosphate. The mesoporous lithiumvanadium phosphate prepared by the method has uniform pores; the contact area between the mesoporous lithium vanadium phosphate and electrolyte is increased; the electron transmission distance is shortened, so that the lithium battery conductivity and the material utilization rate are improved.

The invention relates to a mesoporous surface defect Mn-N-TiO2 microsphere photocatalytic material and a preparation method thereof. The preparation method specifically comprises preparing mesoporous surface defect Mn-TiO2 microspheres and carrying out nitriding treatment, wherein the nitrogen source used for the nitriding treatment is ammonia gas, a surfactant is added during the preparation of the mesoporous surface defect Mn-TiO2 microspheres, and the nitriding treatment is performed in ammonia gas so as to obtain the mesoporous surface defect Mn-N-TiO2 microsphere photocatalytic material. According to the present invention, the metal double-doped titanium dioxide photocatalytic material obtained through the experiment process has characteristics of mesoporous structure and uniform spherical structure.

The invention discloses a preparation and an application of a bifunctional ionic liquid loaded mesoporous polymer. The preparation is characterized by the following steps: taking an imidazole functional ordered mesopore polymer as a carrier, connecting 1,2-dibromoethane and triethylamine in the form of covalent bond, and using sodium acetate and bifunctional ionic liquid for performing ion exchange, thereby acquiring the bifunctional ionic liquid loaded mesoporous polymer. The bifunctional ionic liquid loaded mesoporous polymer is served as a catalyst in the reaction of CO2 and amino compoundfor compounding formamide through heterogeneous catalysis synthesis. Compared with the prior art, the bifunctional ionic liquid loaded mesoporous polymer has the characteristics of large specific surface area of mesoporous material, uniform duct, high heat stability, high chemical stability, and the like; the bifunctional ionic liquid loaded mesoporous polymer is capable of catalyzing the reactionof CO2 and amino compound under a mild condition, has high catalytic activity, can be easily separated and recycled and is reusable; the bifunctional ionic liquid loaded mesoporous polymer is a novelenvironment-friendly catalyst and has a huge development potential in the field of heterogeneous catalysis.

The invention relates to a mesoporous surface defect Ni-N-TiO2 microsphere photocatalytic material and a preparation method thereof. The preparation method specifically comprises: preparing mesoporous surface defect Ni-TiO2 microspheres, and carrying out nitriding treatment, wherein a surfactant is added during the preparation of the mesoporous surface defect Ni-TiO2 microspheres, the nitrogen source for the nitriding treatment is ammonia gas, and the nitriding treatment is performed in the ammonia gas to obtain the mesoporous surface defect Ni-N-TiO2 microsphere photocatalytic material. According to the present invention, the mesoporous surface defect Ni-N-TiO2 microsphere photocatalytic material obtained through the experiment process has the mesoporous structure and has the uniform spherical structure.

The present invention relates to a new lithium ion battery separator and a manufacturing method therefor, composite fine-denier POY fibers with polypropylene PP acting as a core and alkali-soluble polyester COPET and polyethylene PE acting as a skin are produced by means of a chemical fiber composite spinning technology, wherein the COPET and PE are distributed as an islands-in-the-sea form, then the POY fibers are arranged as a fabric with a certain breadth by means of beam-warping, the fabric is subjected to stretching and hot-pressing by a hot roll such that the PE component having a low melting point is melted and joined to form a film, and then the COPET is dissolved away by means of an alkali solution such that a place where the COPET is present in the film become pores and PP fibers become the skeleton of the film, thus forming a lithium ion battery separator.