Abstract: A filter device for filtering particles from an air stream has an inlet channel through which the air to be purified flows, at least one filter element through which the air can flow and which is interchangeably held in a flow channel, and an outlet channel through which the purified air flows, an insertion chamber which can be closed by a door and from which a filter element can be fed to the flow channel, and an output chamber closable by a closure element, into which a filter element is feedable from the flow channel. The closure element of the output chamber is locked in the closed position via a locking mechanism when the door on the insertion chamber is opened and the output chamber and the insertion chamber are connected to the same flow channel.

Abstract: Ethylene-absorbing sachet and method for producing the granulate contained inside same, comprising a packaging formed by two sheets, one anterior (2) and one posterior (3), which are mutually joined along their edges (4) by means of welding, at least one of which, for example, the anterior sheet (2), is manufactured from porous, water-repellent, and breathable material, combined or not with another sheet (3) of impermeable material and with a granulate (5) of ethylene-absorbing material contained inside said packaging, whereby said granulate (5) has a small particle size and lacks fine powder floating in the air and has a high filling density inside the sachet (1); specifically, with a particle size of between approximately 2 and 0.125 mm and a density of between approximately 0.8 and 1.1 g/ml. Said granulate may comprise a substrate impregnated with potassium permanganate or a mixture with activated carbon.

Abstract: The disclosed embodiments relate to the design of a preconcentrator system for preconcentrating air samples. This preconcentrator system includes a plurality of preconcentrators that preconcentrate the air samples prior to chemical analysis, and a delivery structure comprising a manifold that selectively routes a sample airflow to the plurality of concentrators so that the plurality of preconcentrators receive a sample airflow concurrently or individually.

Abstract: The present disclosure relates to a carrier with high capacity which is capable of adsorbing a chlorine dioxide gas at high concentration and a method of preparing a release kit which is capable of releasing the chlorine dioxide gas at a certain concentration for a long period of time, and more particularly, provides a preparation method of a carrier which is capable of adsorbing a high concentration chlorine dioxide gas at high capacity and capable of maintaining a physically and chemically stable state for a long period of time, the carrier including a silica gel, i.e.

Abstract: There is provided an organic iodine trapping apparatus that can efficiently trap an organic iodine without using complicated or large equipment. An organic iodine trapping apparatus 30 is an apparatus that traps an organic iodine, including: a trapping vessel 1 through which gas containing an organic iodine is passed; an organic iodine remover 2 (Example: trihexyl (tetradecyl) phosphonium chloride, or the like) that is disposed in or injected into the trapping vessel 1 and decomposes the organic iodine; and a trapping material 3 that is disposed in or injected into the trapping vessel 1 and traps iodine ions generated by decomposition of the organic iodine, in which the trapping material 3 is a metal (Example: silver or the like) or a metal compound (Example: silver chloride, silver oxide, or the like).

Abstract: A device for exchange of water molecule and temperature between two fluids. The device comprises thin molecular sieve membrane sheets that allow water molecules to permeate through while blocking cross-over of the exchanging fluids. The device provides two sets of flow channels having a hydraulic diameter ranged from 0.5 to 2.0 mm for respective process and sweep fluid flows. The two sets of the channels are separated by a membrane sheet having a thickness less than 200 ?m. The thin molecule sieve membrane may be prepared by forming an ultra-thin zeolite membrane layer on a porous metal-based support sheet which provides very high water permeance so that the exchange can be conducted in a compact membrane module at high throughput. The device can be used to remove water from a process stream of higher water content by use of a sweep fluid of lower water content or higher water affinity.

Abstract: A thermo-sensitive draw solute including a polyoxyalkylene adduct represented by a general formula (1): R1O(AO)nR2 (1), where R1 denotes a residue after withdrawal of a hydroxy group from a monovalent alcohol having a carbon number ranging from 6 to 13, R2 denotes a hydrogen atom or denotes an alkyl group or an alkenyl group having a carbon number ranging from 1 to 13, AO denotes an oxyalkylene group having a carbon number ranging from 2 to 4, n denotes an average added mole number of an alkylene oxide ranging from 1 to 235, and where n is two or more, the two or more AOs may be the same or different from each other.

Abstract: A water purifier includes a water purifier body, a filter bracket provided inside the water purifier body, a pump unit provided inside the water purifier body and including a pump connected to a main water purifying filter installed in the filter bracket, and a vibration transmission-preventing unit which, while the main water purifying filter is installed in the filter bracket, ensures the transmission, to the filter bracket and the water purifier body, of vibrations due to the pressure difference between the pump and the main water purifying filter when water is supplied to the main water purifying filter by means of the pump is reduced by a filter vibration-damping member.

Abstract: The invention relates to a method of determining a permeation property of hollow-fibre membranes wherein the permeation property of the hollow-fibre membrane is determined on a hollow-fibre membrane bundle which has been introduced into a housing and has terminally open hollow-fibre membranes at a first end of the hollow-fibre membrane bundle and terminally closed hollow-fibre membranes at a second end of the hollow-fibre membrane bundle. The invention more particularly relates to a method of determining the ultrafiltration rate and/or the ultrafiltration coefficient of hollow-fibre membranes.

Abstract: The present invention relates to a hollow-fiber membrane module including: a hollow-fiber membrane bundle including a plurality of hollow-fiber membranes bundled in a potting part; a housing enclosing the hollow-fiber membrane bundle; and a protective member contacting with an outer surface of the potting part and continuously covering the outer surface, in which the protective member has a notched part through which one end of the protective member communicates with another end in a longitudinal direction of the hollow-fiber membrane bundle.

Abstract: To regenerate, by a simple method, an inorganic separation membrane separating non-hydrocarbon gas contained in treatment target gas. Provided in separating the non-hydrocarbon gas contained in the treatment target gas is a regeneration gas supply path supplying moisture-containing regeneration gas to a primary side of the inorganic separation membrane in a separation membrane module. As a result, it is possible to regenerate the inorganic separation membrane by supplying moisture-containing CO2 gas to the inorganic separation membrane and then supplying dry natural gas. Accordingly, there is no need to use dry regeneration gas and the CO2 gas supplied via, for example, a pipeline can be used as it is.

Abstract: Described herein are articles for separating gases. The article includes a selective layer consisting of a crosslinked amorphous fluorinated copolymer containing one or more types of fluorinated ring monomers, with crosslinking between the fluorinated copolymer chains. The crosslinking improves the mechanical properties of the fluoropolymer, thereby permitting use of polymer types which would otherwise be excessively brittle. The resulting crosslinked polymer membranes have superior selectivity and reliability performance compared with previous compositions known to the art. Methods for making and using the article described are also provided.

Abstract: A system for making a brine solution is provided comprising: a single conveyor; and a hopper assembly configured to receive a salt and a solvent, the hopper assembly comprising a lower hopper having a shape in which sides of the lower hopper direct any solid contents of the lower hopper, under a force of gravity, towards an entry point of the single conveyor, the hopper assembly further comprising a solvent inlet arranged to spray the salt, wherein the solvent inlet is configured to create a brine solution from a spray of the solvent combined with the salt in the hopper assembly, and wherein the single conveyor is configured to remove debris from the hopper assembly at the entry point of the single conveyor. A novel sediment tank is also provided.

Abstract: An apparatus for aerating bodies of water, comprising a floating platform (19), a motor (15) supported by the floating platform (19), a transmission (16) which is coupled to the motor (15) and whose output shaft is in the form of a hollow shaft (17), a fan for supplying air through an air supply line (18) connected thereto, wherein the air supply line (18) is connected to one end (E1) of the hollow shaft (17), a hollow stirring shaft (1) coupled to the other end (E2) of the hollow shaft (17), an stirrer (K) affixed to the free end of the approximately vertical stirring shaft (1), wherein the stirrer (K) is designated as a hollow body and has a central opening (3) through which air supplied by the stirring shaft (1) can pass, and a multiplicity of air outlet openings (14).

Abstract: An insert assembly for a foam generating device includes a first insert and a second insert with a channel defined therethrough. Inserts may be formed by two shell halves that are coupleable to one another to define the channel. A plurality of ribs extends along an interior surface of the channel. Pad structures defined by porous media are provided in the channel and gripped by the plurality of ribs. The pads receive cleaning solution passing through the channel and cause foam to be generated by breaking-up the cleaning solution and agitating. The ribs may be arranged horizontally relative to a longitudinal axis of the insert assembly and retain the pads within the device. Inserts may be arranged in series along a longitudinal axis of the foam generating device with the pad structures arranged within the channel.

Abstract: A blender includes a blade assembly including a main blade shaft that is coupled to a first blade and a first main coupler so as to rotate in a forward direction and a reverse-rotation blade shaft that is coupled to a second blade and a first reverse-rotation coupler so as to rotate in a reverse direction, a gearbox assembly including a main gear shaft coupled to a second main coupler, which is engaged with the first main coupler, so as to rotate in the forward direction, a plurality of gears configured to convert the forward rotation of the main gear shaft to reverse rotation, and a second reverse-rotation coupler configured to transmit the reverse rotation transmitted through the plurality of gears to the first reverse-rotation coupler, and a case that has the gearbox assembly provided therein.

Abstract: Systems and methods for blending fluids are provided. A blended fluid may be obtained by mixing a first fluid from a first fluid source with a second fluid from a second fluid source. The blended fluid may be pumped by a pump arranged downstream of a point at which the first and second fluids are mixed, wherein no other pumps are upstream of the pump. First and second flow control valves that control the flow rate of the first and second fluids, respectively, are adjusted so as to reach a target flow rate of the blended fluid, the blended fluid having a target blend of the first fluid and the second fluid.

Abstract: A process of granulation of a urea melt, comprising: adding a first additive containing carboxymethyl starch to one or more first stage(s) of the granulation process, to form a carboxymethyl starch containing inner layer of urea granules, and adding a second additive containing calcium lignosulfonate to one or more second stage(s) of the granulation process, downstream said first stages, to form granules with a coating containing calcium lignosulfonate.

Abstract: A reactor system for thermally treating a hydrocarbon-containing stream, that includes a pressure containment vessel comprising an interior chamber and a heat transfer medium that converts electrical current to heat and is positioned within the interior chamber of the pressure containment vessel, wherein the heat transfer medium comprises a first end face, a second end face, and channels extending between the first end face and the second end face. A process for thermally treating a hydrocarbon-containing stream includes introducing the hydrocarbon-containing stream into the reactor system, pressurizing the pressure containment vessel and the heat transfer medium without heating the pressure containment vessel or the heat transfer medium, supplying electrical current to the heat transfer medium, converting the electrical current to heat, heating the hydrocarbon-containing stream, and converting the hydrocarbon-containing stream to an effluent stream.

Abstract: A system for chemical transformation of 3D state materials is disclosed wherein, a reaction group having a main body arranged to shape a reaction chamber in which a component configured to support a sample of 3D state arranged to be chemically transform is expected. The system further includes an oven arranged to heat the reaction chamber and a GAS supply group arranged to release a first gas in the reaction chamber and/or a casing component, inside the main body, which has a chemical agent suitable for releasing a second gas into the reaction chamber. The main body has at least two turbines arranged to converge into the reaction chamber, the first and/or the second gas on the samples. The invention relates also to a method for chemical transformation of 3D state materials.

Abstract: An arrangement for controlling a flow of solid particles includes a vertical inlet pipe for directing solid particles downwards and having a bottom at a level L0, a first outlet chute and a second outlet chute in particle flow connection with the vertical inlet pipe and a fluidizing device for directing controlled first and second sub flows to the first and second outlet chutes. The arrangement includes a branch in particle flow connection with an opening on a side wall of the vertical inlet pipe for directing the first sub flow of solid particles to the first outlet chute and a horizontally extending intermediate pipe for directing the second sub flow of solid particles to the second outlet chute. The intermediate pipe includes at least one nozzle feeding fluidizing gas to the intermediate pipe and has a first end in particle flow connection with the bottom of the inlet pipe.

Abstract: An industrially scalable microcapsule, fiber or film forming process and formulations suitable for use in conventional spray drying systems are provided. The one-step spray drying process utilizes formulations of a first ionic polymer, a second ionic polymer with an isoelectric point (pI2) or acid dissociation constant (pKa2) that is greater than the isoelectric point (pI1) or acid dissociation constant (pKa1) of the first ionic polymer and a volatile base or volatile acid. Volatilization of the volatile base or acid of the spray formulation changes the pH of the solution and changes the charge of the second ionic polymer initiating electrostatic interactions with the first ionic polymer through complex coacervation. Microcapsules formed by the complex coacervation process can stabilize bioactive components as well as control the release of the bioactive components for a variety of applications.

Abstract: Described herein is a new process for the preparation of polysuccinimide derivatives-based core-shell microcapsules. Also described are microcapsules, as well as perfuming compositions and consumer products including these microcapsules, in particular perfumed consumer products in the form of home care or personal care products.

Abstract: A reactor system for thermally treating a hydrocarbon-containing stream includes a pressure containment vessel having an interior chamber defined by a first end, a second end, and at least one sidewall extending from the first end to the second end. A heat transfer medium converts electrical current to heat is positioned within the interior chamber of the pressure containment vessel, and the heat transfer medium has a first end face, a second end face, and channels extending between the first end face and the second end face. A heat sink reservoir includes molten salt, and at least one of a heater or heat exchanger is fluidly coupled to the heat transfer medium and thermally coupled to the heat sink reservoir.

Abstract: Provided are a fine particle manufacturing apparatus and a fine particle manufacturing method, which manufacture smaller fine particles. The fine particle manufacturing apparatus has: a raw material supply unit that supplies raw materials for producing fine particles into a thermal plasma flame; a plasma torch in which the thermal plasma flame is generated and the raw materials supplied by the raw material supply unit is evaporated by the thermal plasma flame to form a mixture in a gaseous state; a plasma generation unit that generates the thermal plasma flame inside the plasma torch; and a gas supply unit that supplies quenched gas to the thermal plasma flame, wherein the gas supply unit supplies the quenched gas with time modulation of the supply amount of the quenched gas.

Abstract: The invention relates to a continuous flow reactor having a wall which delimits a channel, wherein at least one sub-area is arranged in the channel that has microstructuring which includes individual structures, the diameter of which on a base is between about 10 ?m to about 100 ?m. The invention further relates to methods for reacting a gaseous or liquid educt under the action of a catalyst.

Abstract: The present disclosure relates to a packing element, in particular for mass and/or heat exchange columns, through which at least one gas and/or at least one liquid flow flows, comprising a plurality of neighbouring strips curved inwards and/or outwards, wherein each strip is connected to the neighbouring strips at at least one end thereof. It is the object of the present invention to provide a packing element that is improved relative to the state of the art. According to the disclosure, this object is achieved in that at least one of the strips has an irregular shape.

Abstract: There is provided a coating formulation comprising an inorganic oxygen scavenger, a surfactant, an activator, a hydrophilic agent, optionally an additive and a plurality of monomers capable of forming a polymeric matrix, and a method to prepare the same. There is also provided an article comprising an inorganic scavenger, a surfactant, an activator, a hydrophilic agent and optionally an additive dispersed within a polymeric matrix, and a method to prepare the same.

Abstract: A method of removing an organic pollutant from water by contacting the water with a ball milled and sonicated oil fly ash powder to adsorb the organic pollutant onto the ball milled and sonicated oil fly ash powder. A method of producing a ball milled and sonicated oil fly ash powder involving ball milling oil fly ash to provide ball milled oil fly ash particles with an average particle size of less than 1 ?m and sonicating the ball milled oil fly ash particles in an aqueous medium to form the ball milled and sonicated oil fly ash powder. A method of improving recovery of valuable metals/elements from oil fly ash.

Abstract: A sorbent composition for enhanced baghouse function is described. The composition may include a sorbent such as powder activated carbon as well as an additive that is a heat moderator or a permeability agent. The heat moderator may act as a heat sink or barrier. Heat moderators may include in non-limiting examples phyllosilicates, cyclosilicates, or nesosilicates that may include, montmorillonite, bentonite, halloysite, aluminum silicates, muscovite, illite, kaolin, andalusite, kyanite, sillimanite, metakaolin, mullite, polymers, such as chitosan, and/or clays, either natural or synthetic (e.g., montmorillonite), or polyethylenimine. Permeability may be affected by mixing sorbents of lower D50 with sorbents of higher D50 in various ratios, or addition of a permeability agent such as a phyllosilicate, perlite, silica, diatomaceous earth. Further, a permeability agent such as a fluoropolymer may be coated onto or admixed with the sorbent.

Abstract: The present disclosure generally relates to a scalable, green process for producing non-toxic, all-cellulose super absorbent hydrogels that form instantly after cross-linking. A super absorbent hydrogel can be produced by physical mixing of water-soluble carboxyalkyl polysaccharides such carboxymethyl cellulose and negatively-charged cellulose nanocrystals resulting in instantaneous gelation. Cellulose nanocrystals act as effective cross-linkers when physically mixed with carboxymethyl cellulose in an aqueous medium. The resulting hydrogel possesses excellent absorption properties, and has applications in a wide range of products from hygiene products to medical and industrial super absorbent products.

Abstract: A composite comprises a carbonaceous and a metallic nanotube conjugated with a carbonaceous support. The composite may be used to remove contaminants from water.

Abstract: The present disclosure relates to a catalyst that includes a support that includes a metal oxide and a metal deposited on the support, where the metal oxide includes at least one of TiO2, Al2O3, SiO2, CeO2, and/or ZrO2, the metal includes at least one of Pt, Pd, Ru Rh, Ni, and/or Mo, the metal is in the form of a particle, and the metal is present on the support at a concentration between about 0.1 wt % and about 5.0 wt %.

Abstract: In the present disclosure, a composite oxide catalyst capable of effectively suppressing side reactions at the time of dehydrogenation of C4 hydrocarbons having single bonds or one double bond and a process for preparing butadiene, in particular 1,3-butadiene, with a high selectivity and a high yield using the same are described.

Abstract: Provided is a catalyst for purifying exhaust gas, comprising: noble metals; alumina support particles; and TiO2 semiconductor particles supported on the surfaces of the alumina support particles.

Abstract: Methods of producing a catalyst for oxidation of C2 hydrocarbons and methods of using the catalyst are disclosed. Molybdenum, vanadium, and niobium metal or metal containing compounds are used to form a slurry in water. After agitating the slurry for at least 15 minutes, palladium or a palladium containing compound is added to the slurry. After further agitation, a precipitate is collected, dried and calcined to obtain an active catalyst, with palladium primarily distributed on a surface of the catalyst. The active catalyst is capable of catalyzing the conversion of C2 hydrocarbons into acetic acid.

Abstract: The present invention discloses a nickel/titanium oxide-silicon oxide catalyst for synthesizing terpinene-4-ol as well as a preparation method and method of synthesizing terpinene-4-ol using the same. The preparation method includes the steps of catalyst preparation, terpinene-4-ol synthesis and the like are disclosed in the present invention. The preparation method includes the following steps: firstly, preparing a mixed colloid of TiO2 and SiO2 by using a sol-gel method, and then centrifuging, washing, drying and roasting is performed to prepare a TiO2—SiO2 binary oxide; then, preparing Ni/TiO2-SiO2 by dipping in a nickel nitrate solution, and preparing a supported catalyst by drying and roasting; and finally, adopting a terpinolene-4, 8-epoxide a raw material, carrying out isomerization under the dual catalytic action of TiO2-SiO2 and Ni of the supported catalyst, and carrying out hydrogenation to prepare terpinene-4-ol.

Abstract: Catalyst for oxygen storage capacity applications that include a zinc doped manganese-iron spinel mixed oxide material. The zinc doped manganese-iron spinel mixed oxide material may be synthesized by a co-precipitation method using a precipitation agent such as sodium carbonate and exhibits a high oxygen storage capacity.

Abstract: A method of chlorinating a antimony fluorohalide catalyst is disclosed. In one embodiment the method comprises contacting an antimony fluorohalide catalyst that contains one or more fluorines with a regenerating agent chosen from 2-chloro-3,3,3-trifluoropropene (1233xf), 1,1,1,3-tetrachloropropane (250fb), 2-chloro-1,1,1,2-tetrafluoropropane (HCFC-244bb) and combinations of 1233xf, 250fb, and 244bb, under conditions effective to exchange at least one fluorine in the antimony fluorohalide catalyst with chlorine. The method can be used to regenerate spent antimony fluorohalide catalyst, for example regenerating SbCl5 from SbF5.

Abstract: A fluid catalytic cracking catalyst for hydrocarbon oil that is a blend of two types of fluid catalytic cracking catalysts each of which has a different hydrogen transfer reaction activity or has a pore distribution within a specific range after being pseudo-equilibrated. One catalyst is a catalyst containing a zeolite and matrix components, and the other catalyst is a catalyst containing a zeolite and matrix components. This catalyst is composed of the one catalyst and the other catalyst blended at a mass ratio within a range of 10:90 to 90:10.

Abstract: A method of making a xylene isomerization catalyst comprises the steps of (i) contacting a ZSM-5 zeolite starting material having a silica to alumina molar ratio of 20 to 50 and having a mesopore surface area in the range of 50 m2/gram to 200 m2/gram in a reactor with a base to provide an intermediate zeolite material; (ii) recovering the intermediate ZSM-5 zeolite material of step (i); (iii) contacting the intermediate zeolite material with an acid to provide an acid treated ZSM-5 zeolite product; (iv) recovering the acid treated ZSM-5 zeolite material; and (v) calcining the acid treated ZSM-5 zeolite material to provide a desilicated ZSM-5 zeolite product having a silica to alumina molar ratio of 20 to 150 and having a mesopore surface area in the range of 100 m2/gram to 400 m2/gram.

Abstract: A hydrogenolysis bimetallic supported catalyst comprising a first metal, a second metal, and a zeolitic support; wherein the first metal and the second metal are different; and wherein the first metal and the second metal can each independently be selected from the group consisting of iridium (Ir), platinum (Pt), rhodium (Rh), ruthenium (Ru), palladium (Pd), molybdenum (Mo), tungsten (W), nickel (Ni), and cobalt (Co).

Abstract: The present disclosure discloses a core-shell structured NiSe2@NC electrocatalytic material having a general formula of NiSe2@NC. The present disclosure also provides a preparation method and use of the catalytic material. In the present disclosure, hydrazine hydrate is used as a reducing agent, selenium powders are used as a source of selenium, and a metal-organic framework (MOF) is used as a precursor. Selective selenization of mixed-linker MOFs based on mixed ligands is carried out through a hydrothermal reaction. Then, a series of adjustable N-doped carbon-coated NiSe2 nano-octahedrons are prepared through a one-step calcination reaction. By adjusting the types of mixed ligands in the MOF, carbon-coated nickel diselenide composites doped with different pyridinic-N contents can be obtained. Corresponding electrochemical tests prove that, the electrocatalytic activity has a strong correlation with the content of pyridinic-N.

Abstract: The present disclosure provides a Lewis acid-base pair catalytic initiator and an application thereof. The Lewis acid-base pair catalytic initiator includes a Lewis acid and a Lewis base, the Lewis acid having a structural general formula as shown in formula (I) and the Lewis base having a structural general formula as shown in formula (II); wherein: the A is selected from element Baron or element Aluminum; the R1, R2, R3, R4 are independently selected from alkyl, alkoxy, aryl or halogen groups; the alkyl or alkoxy have a carbon number being equal to or greater than 1 to equal to or less than 16; the aryl contains substituents with the number being equal to or less than 5, the substituents being selected from methyl, methoxy or halogen; n is selected from an integer from 1 to 16.

Abstract: The invention relates to a material in the form of a cellular solid monolith consisting of an inorganic oxide polymer. Said monolith comprises macropores which have an average size dA of 4 ?m to 50 ?m, mesopores that have an average size dE of 20 to 30 ?, and micropores which have an average size d1 of 5 à 10 ?, said pores being interconnected. The inorganic oxide polymer has organic groups R of formula —(CH2)n—R1, wherein 0?n?5, and R1 is selected from among a thiol group, a pyrrole group, an amino group having one or more optional, optionally substituted alkyl, alkylamino, or aryl substituents, an alkyl group, or a phenyl group optionally having an alkyl-type substituent R2. The disclosed material can be used as a substrate for a metal catalyst and for decontaminating liquid or gaseous media.

Abstract: Described herein is a simple and versatile synthetic strategy for the preparation of metal-organic frameworks comprising a carbon matrix doped with nitrogen atoms, wherein transition metal ions are bonded to the carbon matrix via the nitrogen atoms. This strategy is applicable for the synthesis of single metal catalysts or multi metal catalysts rich with atomically dispersed metal active sites. The metal-organic frameworks provided herein have numerous application when used in fuel cells.

Abstract: Carbon-based single metal atom or bimetallic, trimetallic, or multimetallic alloy transition metal-containing catalysts derived from exoelectrogen bacteria and their methods of making and using thereof are described. The method comprising the steps of: (a) preparing a solution medium comprising at least an electron donor and an electron acceptor comprised of one or more salts of a transition metal; (b) providing exoelectrogen bacterial cells and mixing the exoelectrogen bacterial cells into the solution medium of step (a); (c) incubating the solution medium of step (b); (d) isolating the exoelectrogen bacterial cells from the incubated solution medium of step (c); and (e) pyrolyzing the exoelectrogen bacterial cells resulting in formation of the catalyst. The electron donor can be formate, acetate, or hydrogen.

Abstract: A method of manufacturing a catalyst material includes the steps of: providing a body having an open-porous foam structure and comprising at least a first metal or alloy; providing particles, each of which particles comprising at least a second metal or alloy; distributing the particles on the body; forming a structural connection between each of at least a subset of the particles and the body; and forming an oxide film on at least the subset of the particles and the body, wherein the oxide film has a catalytically active surface.

Abstract: The present invention provides a method for producing a catalyst for ammoxidation, comprising steps of: preparing a catalyst precursor slurry comprising a liquid phase and a solid phase; drying the catalyst precursor slurry to obtain dry a particle; and calcining the dry particle to obtain a catalyst for ammoxidation, wherein the solid phase of the catalyst precursor slurry comprises an aggregate containing a metal and a carrier, metal primary particles constituting the aggregate have a particle size of 1 ?m or smaller, and an average particle size of the metal primary particles is 40 nm or larger and 200 nm or smaller.

Abstract: The present disclosure discloses a process for improving the surface catalytic efficiency of a catalyst substrate. In some embodiments, to use nano-catalyst particles more efficiently, a process uses a porous substrate as a stationary phase support and disperses the nano-catalyst particles uniformly in all the internal space of the porous substrate, such that reactants flow through the porous substrate to achieve a catalytic effect. In some embodiments, the process not only improves the use efficiency of nano-catalyst particles, but also enables easier and more convenient adjustment of various parameters of a catalytic reaction.