1591 results about "Macropore" patented technology

An improved porous ceramic biomaterial is disclosed in which a polymer such as polylactic acid is polymerized in situ to fill the micropores substantially without filling the macropores. The polymer reinforcement helps improve the strength of the implant while preserving its ability to support ingrowth of bone to help integrate the implant into its surgical environment.

The invention relates to a method for preparing a carbon material with rich mesopores and macropores. Inorganic nano-particles are used as pore-forming template agent to be uniformly distributed in a carbon-contained organic precursor and then the carbon-contained organic precursor carries out high-temperature carbonization, template agent washing-out and drying to obtain a porous carbon material. The carbon material prepared by the method has the specific surface area of 50-1,900 m / g and a pore diameter mainly between 2-900 nm, can be conveniently adjusted by the size control of the selected nano-particles, removes a template without using high corrosive HF and has the advantages of simple method, convenient operation, free pore diameter adjustment and control in a mesopore and macropore range, and the like. The carbon material has a wide application prospect in fields of electrochemical energy accumulation, macromolecular adsorption, catalyst carriers, composite materials, and the like.

A carbon monolith includes a robust carbon monolith characterized by a skeleton size of at least 100 nm, and a hierarchical pore structure having macropores and mesopores.

A bone replacement material and therapy comprises the combination of calcium phosphate compounds and two or more soluble fillers in the form of fibers, mesh or other materials which have the dual functions of reinforcing an in vivo implant while dissolving at a programmed rate to form macropores capable of receiving natural bone ingrowth.

The invention discloses coal gangue lightweight through-hole ceramsite. The technical scheme has the essentials that the coal gangue lightweight through-hole ceramsite is composed of coal gangues, attapulgite clay, a powdery coal gangue foaming agent, active carclazyte waste dreg, hollow microspheres, lightweight magnesium oxide, expanded perlite, expanded vermiculite, ferrous sulfate and quick lime. The materials of the coal gangue lightweight through-hole ceramsite are stirred and mixed, extruded and granulated, dried, roasted, subjected to heat insulation, sieved, sealed and packaged to prepare the coal gangue lightweight through-hole ceramsite. The coal gangue lightweight through-hole ceramsite has the characteristics of large specific surface area, small bulk density, high water absorption rate, excellent ventilation performance, beautiful appearance and shape and no odors, no harmful bacteria, good lightweight strength, and consistent micro-pores and macro-pores. When the coal gangue lightweight through-hole ceramsite is used for culturing or planting various types of nursery stocks, flowers and vegetables, the roots of the plants can absorb nutrition constituents of water or a liquid fertilizer from the coal gangue lightweight through-hole ceramsite, so that good growth and development and the survival rate of the plants are ensured and the coal gangue lightweight through-hole ceramsite is suitable for preparing a soilless culture substrate and nutrient soil.

The invention provides nitrogen mixed grapheme hydrogel of which the water content is 90 to 99.5 percent, the electric conductivity is 10-3-100 S / m, and the molar ratio of N and C is 1 to 25 percent. The invention further provides nitrogen mixed aerogel of which the molar ratio of N and C is 2 to 20 percent, the molar ratio of C and O is 15 to 5, nitrogen atoms existing in the form of amidogen nitrogen accounts for 40 to 70 percent, pyridine type nitrogen accounts for 10 to 40 percent, graphite type nitrogen accounts for 10 to 30 percent, the specific area is 300 to 1500 m<2> / g, the apertures which are micropore account for 10 to 20 percent, the apertures which are mesoporous 20 to 50 percent, the apertures which are macropore 30 to 70 percent, the apparent density is 0.01 to 0.2 g / cm<3>, the pore volume is 5 to 20 cm<3> / g, and the electric conductivity is 1 to 1000 S / m. The nitrogen mixed grapheme hydrogel or aerogel and preparation method thereof provided by the invention has the characteristics that the operation is simple, the equipment requirement is low, the production efficiency is high, the scale-up of the technology is easy, the nitrogen mixed content is controllable and the compounding with other functional substances is simple.

The invention provides a three-dimensional ordered macroporous alumina and a preparation method thereof, wherein the method comprises the following steps of: assembling polymer microspheres which are singly dispersed to form a colloidal crystal template, filling the alumina sol which is prepared by means of a special method into the template, and drying and roasting to obtain macroporous alumina. The method provided by the invention has the advantages that the alumina sol and the compounding process of the alumina sol and the polymer microspheres can be controlled well, the network structure of the alumina sol is protected possibly, the alumina which is prepared by means of the method not only has three-dimensional ordered macroporous channels but also has a high specific surface area. Furthermore, the macropores within the material are communicated to the surrounding macropores by means of 12 small window holes, and the window holes are formed by sintering the template properly. The alumina prepared by means of the method provided by the invention is suitable for being used as a catalyst carrier of heavy oil and an adsorption and separation material of organic macromolecule. The alumina prepared by means of the method which is provided by the invention is suitable for improving the mass transfer capability of the material within the catalyst and is suitable for improving the activity and the selectivity of the catalyst during the application process as a catalyst carrier.

The invention discloses a preparation method of a nitrogen-doped porous-structure carbon material and belongs to the technical field of inorganic material preparation. The preparation method utilizes a micromolecular carbon-containing compound as a raw material and comprises the following steps of based on the weight of the raw material, adding 0-400wt% of an inorganic base, 0-400wt% of an organic nitrogen-containing compound and 0-50wt% of a metal or metal oxide or inorganic metal salt into the raw material, carrying out uniform dispersion, and carrying out a reaction process in an inert gas protective atmosphere at a temperature of 400-900 DEG C for 0.5-12h so that the nitrogen-doped porous-structure carbon material having micropores, mesopores and macropores is obtained. The preparation method has simple processes, can be controlled easily, and realizes one-step combination of porous structure, functionalization nitrogen doping and metal particle modification. The nitrogen-doped porous-structure carbon material having high nitrogen content has a large capacitance value and good cycle performances, can be used as an oxygen reduction reaction catalyst having high activity, high selectivity and high stability and has a very large application prospect.

The present invention relates to the separation of one or more of CO2, N2, and H2S gas components from a gas mixture containing at least a second gas using a swing adsorption process unit. The adsorbent contactors of the swing adsorption process unit are engineered structured adsorbent contactors having a plurality of flow channels wherein 20 volume percent or less of the open pore volume of the contactors is in the mesopore and macropore range.

Provided are fibrous composites prepared by methods of the present invention, comprising oxides and biodegradable polymers, in which the fibers are made of aerogel-like oxide materials having nanometer-sized pores. The fibrous composition advantageously has, at least, the following characteristics: (i) a very high nanoporous surface area, which also permits nucleation of crystallites; (ii) mesoporous / macroporous interspacial networks between the fibers, providing high bioactivity and a high transport rate; (iii) macropores for natural one-like tissue growth; (iv) good mechanical properties for handling and for implant support; and (v) biodegradability for implant dissolution and time-variable mechanical properties. Further provided are methods for using the bioactive biodegradable fibrous composites as osteogenic composite materials for tissue engineering, tissue re-growth, bone implants, and bone repair, and / or for the delivery of drugs or therapeutic compounds.

The invention concerns high-performance adsorbents based on activated carbon of high meso- and macroporosity which are present in the form of discrete grains of activated carbon, whereinat least 55% of the total pore volume of the high-performance adsorbents are formed by pores (i.e. meso- and macropores) having pore diameters of more than 20 Å,the high-performance adsorbents have a measure of central tendency pore diameter of more than 25 Å, andthe high-performance adsorbents have a BET surface area of at least 1250 m2 / g.These high-performance adsorbents are obtainable by a novel process comprising specific two-stage activation, and have, in addition to the aforementioned properties, an excellent abrasion and bursting resistance, so that they are useful for a multiplicity of different applications.

The invention discloses a micro-porous alumina carrier and relative preparing method, which contains boric oxide and another agent selected from phosphor, silicon, zirconium, and titanium. The invention adds the boric acid into water or peptizate acid whose temperature is higher than room temperature, then adds the mixture of alumina leading material and physics expanding-hole agent to be molded, dried, and burnt to attain the final carrier. The inventive carrier contains a proper agent, with the characters of large aperture, centralized distribution hole and a certain acid. And its surface acid and aperture can be adjusted easily. Therefore, the invention can overcome the defects of present technique which can not have aforementioned characters at the same time. The inventive alumina carrier can be used in variable hydrogenation catalyst.

The invention provides a preparation method of porous structured active carbon. The preparation method comprises the following steps of: drying animal bones serving as raw materials; pre-carbonizing at the temperature of 400 to 500 DEG C under the protection of an inert gas; crushing into powder; adding an activating agent into the powder; performing chemical activation under the protection of the inert gas; cooling and taking a product out; and performing aftertreatment process such as acid-washing, water-washing and drying to obtain the porous structured active carbon, wherein the product prepared at 850 DEG C has the specific surface area of 2,157 square meters per gram and the pore volume of 2.26 cubic centimeters per gram; the pores are in a three-dimensional distribution of micropores, mesopores and macropores. By taking organic substances and inorganic substances in the animal bones as a carbon source and a natural template with a special pore structure, the preparation method overcomes the defects of requirement on a template and difficulty in immersing pores in a template by using a carbon precursor, prepares the porous active carbon, and is low in cost and simple in process.

A clay stabilizer which is capable of inhibiting swelling in a wide variety of clay types and is also capable of restoring permeability in formations which have previously been damaged by clay swelling. Amine salts of differing molecular weights configurations and ionic strength are combined to provide transport into micropores, mesopores and macropores in the formation and to effect cationic change therein. A poly quaternary amine having a high to very high charge density is added along with lower molecular weight amine salts to substantially permanently exchange cations with the clay in the formation.

The invention relates to a calibration method for representing dense sandstone pore size distribution by adopting nuclear magnetic resonance; the method comprises the steps of measuring the rock porosity and the skeleton density; carrying out a low-temperature broken sample N2 absorption and desorption experiment, and carrying out a nuclear magnetic resonance test and a high pressure Hg injection test on a regular column sample in a saturated formation water state; converting pore volume obtained through N2 absorption into porosity components under different pore throat radiuses by using a capillary accumulated Hg inlet curve, and establishing a pore proportion summation curve by synthesizing low temperature N2-high pressure Hg injection; determining a best calibration coefficient by comparing the nuclear magnetic resonance pore proportion summation curves under the different C values to realize the conversion between nuclear magnetic resonance T2 spectrum and the pore throat radius; establishing a relation between parameters of the calibration coefficient C and a reflection pore-throat structure according to lithological characters; carrying out nuclear magnetic resonance conversion on dense sandstone reservoirs which are positioned in the same region and have the same lithological character. According to the method, the nuclear magnetic resonance T2 spectrum is calibrated by combining low temperature N2 absorption and a high pressure Hg injection experiment, and large pores, micropores and mesopores are calibrated, so that the distribution of different grades of pore sizes in dense sandstone can be effectively represented.

Provided is a preparation method of a porous ceramic material rapidly formed based on photocuring. The preparation method comprises the steps that firstly, a photo-cured resin prepolymer, an active diluent and a surface modifier are evenly mixed to obtain a premixed solution, ceramic powder and a pore-forming agent are mixed to obtain porous ceramic powder, then the porous ceramic powder is mixed in the premixed solution to obtain primary slurry, and then a photoinitiator is added to prepare a photocured porous ceramic slurry; the ceramic slurry is put in a photocuring forming device to prepare a photocuring forming blank; finally the blank is degreased and sintered to obtain the porous ceramic material. By designing and optimizing the components and proportion of the photocured porous ceramic slurry and using a photocuring 3D printing device, the limitations of traditional mold processing to shapes are overcome. The micropores formed by adopting the pore-forming agent and macropores for 3D printing are combined, and the high-porosity foam ceramic material can be prepared. In addition, the macropores are controllable in shape and distribution, and gradient porous ceramic material can be prepared.

This invention relates to doped catalysts on an aluminosilicate substrate with a low content of macropores and the hydrocracking / hydroconversion and hydrotreatment processes that use them. The catalyst comprises at least one hydro-dehydrogenating element that is selected from the group that is formed by the elements of group VIB and group VIII of the periodic table and a dopant in a controlled quantity that is selected from among phosphorus, boron, and silicon and a non-zeolitic substrate with a silica-alumina base that contains a quantity of more than 15% by weight and of less than or equal to 95% by weight of silica (SiO2).

The invention discloses a composite lithium ion battery diaphragm comprising a nonwoven fabric substrate layer, an electrostatic spinning layer and a polymer porous coating, and the structure compound mode is as follows: polymer porous coating / electrostatic spinning layer / nonwoven fabric substrate layer / electrostatic spinning layer / polymer porous coating; nonwoven fabric substrate layer / electrostatic spinning layer / polymer porous coating; or polymer porous coating / nonwoven fabric substrate layer / electrostatic spinning layer / polymer porous coating. The composite lithium ion battery diaphragm uses nonwoven fabric as a substrate to ensure the diaphragm high porosity and heat resistance, electrostatic spinning layers are arranged on the upper and lower surfaces of the nonwoven fabric substrate, the nonwoven fabric pore diameter can be reduced, the pore diameter is uniform, and the problem of short circuit caused by local macropore of the nonwoven fabric diaphragm can be solved, and by the arrangement of the polymer porous coating, the absorption and electrolyte maintaining capacity of the diaphragm can be improved, battery positive and negative electrodes can be bonded, battery mechanical properties can be improved, and the battery safety can be ensured. The prepared composite lithium ion battery diaphragm can satisfy the security requirements of large current charging discharging and running in harsh environments of a high-capacity high-power power battery.

The invention relates to a method for purifying electroplating wastewater and comprehensively utilizing resources, which is to adopt low-cost strong basic anion-exchange resin containing macropores and imidazole structure to reclaim valuable resources in the electroplating wastewater by coupling technology based on a chemical oxidation-reduction method, a precipitation method and an ion exchange method. The method comprises the following steps: firstly, Cr(III) is oxidized into Cr(VI) under basic condition through a chemical reaction; then, Zn, Cu, Ni and other heavy metal elements in the wastewater are transformed into precipitation of hydroxide; and finally, the Cr(VI) in the wastewater is adsorbed by the strong basic anion-exchange resin, the purified water quality achieves the requirement of electroplating pollutant discharge standard and recycle, and the Cr and other heavy metal resources in the electroplating wastewater can be comprehensively reclaimed and utilized. The method overcomes the defects that the prior regenerating process of porous weak-basic resin requires acidification, and the method has the advantages of simple process, low treatment cost, large treatment quantity and acid and base consumption conservation, and is the electroplating wastewater treatment method with green environmental protection and efficient utilization of resources.

The invention provides a coordination polymer material with a multistage pore passage structure and a preparation method thereof. The coordination polymer material with a multistage pore passage structure is internally provided with the multistage pore passage structure, the multistage pore passage structure is a microporous and / or mesoporous and / or macroporous multistage pore passage structure which is formed by the self assembly between the metal ion and the organic ligand, the apertures of the micropores are less than or equal to 2nm, the apertures of the mesopores are from 2nm to 50nm, and the apertures of the macropores are more than 50nm. The coordination polymer material with a multistage pore passage structure is large in specific surface, the large-size organic ligand does not need to be synthesized, and the coordination polymer material with larger porous sizes can be obtained without the template agent and the pore assisting agent, so that the invention is simple in preparation method, and low in cost.

Provided herein are methods for preparing nano-macroporous glass articles, such as bioscaffolds, from starting materials such as phosphosilicate glasses made by melt-quench methods, mixed with a soluble pore former such as a sugar, followed by steps of dissolving, heating, and leaching to yield a glass composition having a highly interconnected system of both macropores and large scale nanoporosity.

The invention relates to a catalyst including at least one hydro-dehydrogenating element chosen from the group formed by the group VIB and group VIII elements of the periodic table and a substrate based on a silica-alumina matrix with a reduced content of macropores containing a quantity greater than 5% by weight and less than or equal to 95% by weight of silica (SiO2) and based on at least one zeolite. The invention also relates to a substrate based on a silica-alumina matrix with a reduced content of macropores containing a quantity greater than 5% by weight and less than or equal to 95% by weight of silica (SiO2) and based on at least one zeolite. The invention also relates to hydrocracking and / or hydroconversion processes and hydrotreating processes utilising a catalyst according to the invention.

In one aspect, the present invention relates to a synthetic nanostructure. In one embodiment, the synthetic nanostructure has a top region substantially comprising titanate nanowires, a middle region substantially comprising titanate nanoparticles and titanate nanowires, and a bottom region substantially comprising titanium, wherein some of the titanate nanowires of the top region are extending into the middle region, wherein the middle region is between the top region and the bottom region, and wherein some of the titanate nanowires of the top region are substantially perpendicular to the bottom surface of the titanium substrate. At least some of the titanate nanowires in the top region form 3D macroporous scaffolds with interconnected macropores.

An inorganic monolithic material that includes macropores having an inner surface and nanoparticles attached to the inner surface of the material. The macropores and the nanoparticles can be optionally attached to molecular moieties that impart a specific functionality to the material. The material has particular applications to separations and chromatography.

Silica gel is impregnated as an impregnating substance into pores of an activated carbon having mesopores and macropores. Since the mesopores and the macropores are impregnated with the silica gel, they are made narrow and small whereby a pore size ratio within a range of 1 to 10 nm is increased.

Macroporous 3-D tissue engineering scaffold comprising elastomeric cross-linked polymer units and interconnected macropores containing living cells are produced by step of: in a mixture of the cells and elastomeric polymer units comprising activatable crosslinking groups, activating the crosslinking groups to form the scaffold.

The invention concerns an improved hydrocracking process with a recycle having a step for eliminating polyaromatic compounds from at least a portion of the recycled fraction by adsorption on a particular adsorbent based on alumina-silica with a controlled macropore content.