Abstract: The two-dimensional metal carbide desalination membrane includes a stack of two-dimensional metal carbide layers. A two-dimensional metal carbide included in the two-dimensional metal carbide layers may have the formula Ti3C2Tx, where T represents a terminating functional group, and x represents a number of the terminating functional groups. The terminating group may be oxygen, hydroxide (OH), fluorine or combinations thereof. The two-dimensional metal carbide desalination membrane includes nano-channels which are selectively permeable to ions. The two-dimensional metal carbide desalination membrane is selectivity permeable to a number of different cations, including Li+, Na+, K+, Mg2+, Ca2+, Ni2+ and Al3+, with counter Cl? anions. Permeation rates depend on the charges of the cations and the ions' hydrated radius, with a critical point around 4.0 ?. The two-dimensional metal carbide desalination membranes can be used as desalination and/or water filtration membranes.

Abstract: Embodiments of the present disclosure provide for composite materials, methods of making composite materials, methods of using composite materials, and the like. In particular, the present application relates to hollow fibers and to pressure-retarded osmosis systems comprising said fibers. The hollow fibers have an inside layer and an outside layer, wherein the outside layer covers an outside surface of the inside layer, wherein the inside layer forms a boundary around the lumen, wherein the inside layer includes a bi-layer structure, wherein the bi-layer structure includes a sponge-like layer and a finger-like layer, wherein the sponge-like layer is disposed closer to the lumen of the hollow fiber and the finger-like layer is disposed on the sponge-like layer on the side opposite the lumen, wherein the outside layer includes a polyamide layer.

Abstract: The embodiments described herein relate to agarose ultrafiltration membrane composites and methods for making and using the same.

Abstract: A gas separation membrane, characterized by having a porous support and a polyamine layer formed on the porous support, the number-average molecular weight of the polyamine constituting a part of the polyamine being 100,000-500,000.

Abstract: A mounting assembly is provided, including: a drive coupler shaped to engage a coupling member on a shaft positionable within a container defining an aperture to allow passage of the shaft; and a funnel positioned within the aperture to receive the drive coupler and guide the drive coupler to the coupling member. The assembly provides ergonomic advantages as the user is not required to lift the drive to reach the aperture.

Abstract: The device for adjusting the concentration of a gas in a liquid includes a cartridge in which the concentration of the gas in the liquid is adjusted, a pipe for supplying the liquid into the cartridge, a pipe for supplying gas into the cartridge, and a pipe for discharging the liquid from the cartridge. The gas supply pipe includes an expansion valve with of which the pressure setpoint that is controlled by a setpoint for the quantity amount of gas in the liquid and by an amount of a quantity of gas in the liquid measured by a gas concentration sensor located in the liquid discharge pipe.

Abstract: A method, apparatus, and system for obtaining a solution from a solid product are disclosed. A solid product is housed in a dispenser. A liquid is introduced into the housing of the dispenser to interact with the solid product to form a solution. To control the concentration of the formed solution, the turbulence of the liquid introduced to the dispenser is controlled and adjusted either manually or on a real time basis to account for varying characteristics of either or both of the solid product and the liquid. The dispenser will adjust the turbulence based on the characteristics to maintain a formed solution within an acceptable range of concentration. The concentrated solution can then be discharged from the dispenser to an end use application.

Abstract: A system for evolving and dissolving a gas with a liquid can include a pressure vessel in which a liquid mixed with a gas is disposed, and a gas source coupled to the pressure vessel. The system can also include at least one regulating device that regulates a parameter within the pressure vessel. The system can further include at least one sensor that measures at least one parameter as a function of time, where the at least one parameter is associated with the gas within the pressure vessel. The system can also include a controller that controls the regulating device based on measurements of the at least one parameter taken by the at least one sensor, to evolve and dissolve the gas within the pressure vessel.

Abstract: A beverage stirring assembly for selectively stirring a liquid in a container includes a container that may contain a liquid. A stirring unit is removably coupled to the container and the stirring unit is selectively manipulated. The stirring unit stirs the liquid when the stirring unit is manipulated. Moreover, the stirring unit is selectively removed from the container thereby facilitating an interior of the container to be washed.

Abstract: A pouring shield for a stand mixer includes an upper collar for mounting to a mixer head of the stand mixer in a friction-fit manner without the need for clamps or other mounting accessories. The stand mixer is configured to receive a mixing bowl with an open top, and the pouring shield is configured to cover the open top of the mixing bowl at an upper rim of the mixing bowl using a seal member which is disposed around an outer perimeter of the pouring shield. The seal member is a flexibly resilient member configured to close the open top of the mixing bowl when the stand mixer is in a closed position, and includes a wide surface for accommodating mixing bowls of various sizes.

Abstract: The present invention describes a device that firstly allows temporary storage of a certain quantity of catalyst and, secondly, the putting back into circulation of said quantity in the regenerative reforming installations following an interruption in the circulation of the catalyst.

Abstract: A method is provided for upgrading a hydrocarbon feed. The method may include contacting a hydrocarbon feed with a catalyst in a fluidized bed reactor; directing a portion of the catalyst from the fluidized bed reactor to a regeneration zone, such that the portion of the catalyst flows in a first direction through the regeneration zone; directing combustion air into the regeneration zone in a counter-flow direction to the first direction, wherein the combustion air is provided at a rate of about 100.05% or less of the stoichiometric air requirement for combusting coke present on the portion of catalyst; regenerating the portion of the catalyst in the regeneration zone to produce regenerated catalyst; and directing a portion of the hydrocarbon feed to combine with the regenerated catalyst downstream of the regeneration zone and lift the regenerated catalyst back to the fluidized bed reactor.

Abstract: An encapsulated perfume composition comprising at least one perfume-containing aminoplast core-shell microcapsule dispersed in an aqueous suspending medium, the microcapsule being characterized in that it bears a positive charge.

Abstract: A sealing assembly creating a sealed flow path between fluid ducts. The seal assembly comprises a housing and a tubular element within the housing providing a fluid conduit between the fluid ducts. Two sealing elements each have an internal sealing face sealably engaged with the tube and an external face for sealing, in use, with a respective fluid duct. At least one of the sealing elements is slidable with respect to the tubes. A support is slidably retained by the housing, surrounds one end of the tube and supports one of the slidable sealing elements on the side of the sealing element opposite to its external face. A resilient element within the housing biases the support so as to urge the two sealing elements apart.

Abstract: Apparatus and methods utilizing induction-heat energy for heating reactions associated with chemical synthesis, such as peptide synthesis reactions involving activation, deprotection, coupling, and cleavage. Thorough agitation of the contents of reaction vessels during heating, real-time monitoring and adjustment of temperature and/or reaction duration, independent control of different reaction vessels, and scalability are also described.

Abstract: An apparatus for producing an inorganic powder and an apparatus for producing and classifying an inorganic powder are provided, wherein the apparatus for producing an inorganic powder includes an insulating tube, at least one pair of annular RF electrodes, and a gas supply apparatus. The pair of annular RF electrodes surrounds the outer circumference of the insulating tube to generate a first electric field region outside the insulating tube and generate a second electric field region having a plasma torch in the insulating tube after being turned on. The gas supply apparatus supplies a reaction mist and an inert gas into the insulating tube to thermally degrade and oxidize the reaction mist into an inorganic powder via the plasma torch.

Abstract: The invention relates to a process for the preparation of one or more intermediate chemical compounds useful in the preparation of non-ionic contrast agents wherein the process is carried out continuously using one or more flow procedures.

Abstract: There is provided a method of harnessing ambient thermal energy including: conducting an endothermic reaction in thermal contact with a first heat sink to generate one or more reaction products and conducting an exothermic reaction in thermal contact with a second heat sink using at least one of the one or more reaction products. The conducting the endothermic reaction and the conducting the exothermic reaction generates a temperature difference between the first heat sink and the second heat sink.

Abstract: A method is described for preparing a sorbent precursor comprising the steps of: (i) forming agglomerates comprising a particulate support material, (ii) coating the agglomerates with a coating mixture powder comprising a particulate sulphidable copper compound and a particulate calcined, rehydratable alumina to form a coated agglomerate, and (iii) drying the coated agglomerate to form a dried sorbent precursor. The sorbent precursor may be sulphided and used to remove heavy metals such as mercury from fluid streams.

Abstract: Adsorbent clarification agents suitable for use in bioprocessing procedures are disclosed. Methods of making and using the adsorbent clarification agents are also disclosed.

Abstract: The present disclosure pertains to methods of capturing CO2 from an environment at pressures above 1 bar by associating the environment with a porous material that has a surface area of at least 2,800 m2/g, and a total pore volume of at least 1.35 cm3/g, where a majority of pores of the porous material have diameters of less than 2 nm. The present disclosure also pertains to methods for the separation of CO2 from natural gas in an environment at partial pressures of either component above 1 bar by associating the environment with a porous material that has a surface area of at least 2,200 m2/g, and a total pore volume of at least 1.00 cm3/g, where a majority of pores of the porous material have diameters of greater than 1 nm and less than 2 nm.

Abstract: Porous organic compositions including a core comprising nitrogen-containing molecules and a shell comprising nitrogen-containing compounds wherein the shell is non-chemically bonded to the core are provided herein. Processes for making the porous organic compositions as well as gas separation processes using the porous organic compositions are also provided herein.

Abstract: Functionalized metal-organic framework adsorbents with ligands containing basic nitrogen groups such as alkylamines and alkyldiamines appended to the metal centers and method of isolating carbon dioxide from a stream of combined gases and carbon dioxide partial pressures below approximately 1 and 1000 mbar. The adsorption material has an isosteric heat of carbon dioxide adsorption of greater than ?60 kJ/mol at zero coverage using a dual-site Langmuir model.

Abstract: An electronic vaping device includes a housing extending in a longitudinal direction, a reservoir in the housing, the reservoir configured to store a pre-vapor formulation, a heater in the housing, the heater configured to heat the pre-vapor formulation, at least one portion formed of a material including at least one polymer and at least one oxygen sequestering agent, and a power supply.

Abstract: A super absorbent thermochromic resin and a preparation method thereof are disclosed. The resin comprises the following components by weight percent: 30-60% of a monomer, 0.01-0.5% of an initiator, 0.01-4% of a dispersant, 0.01-5% of a cross-linking agent, 0-20% of a diluent, 0.5-2% of an auxiliary, 0.1-10% of a thermochromic pigment, and the balance of water. Compared with the prior art, the super absorbent thermochromic resin prepared by the present invention can effectively indicate the temperature changes of the resin in a drying state and a water absorption state through color changes. The reaction finishes in 6-10 min, with a simple process, smooth polymerization, short reaction time and high productivity. The super absorbent thermochromic resin has a good stability and can be widely applied to the medical industry and daily use articles industry.

Abstract: A solid form adsorbent including a plurality of discrete adsorbent particles spatially bound in place by point bonding by a binder. At least about 25% of the external surface area of a majority of the particles is not sealed off by the binder and is available for adsorption.

Abstract: A method and system for manufacturing and using a self-supporting structure in processing unit for adsorption or catalytic processes. The self-supporting structure has greater than 50% by weight of the active material in the self-supporting structure to provide an open-celled structure providing access to the active material. The self-supporting structures, which may be disposed in a processing unit, may be used in swing adsorption processes and other processes to enhance the recovery of hydrocarbons.

Abstract: A water absorption treatment material includes a core portion and a coating portion. The core portion is approximately circular column-shaped and has a side surface, a first bottom surface, and a second bottom surface. The coating portion is provided so as to cover the core portion. A region of 80% or more of the side surface of the core portion is covered by the coating portion. A region of 80% or more of the first bottom surface of the core portion is exposed without being covered by the coating portion.

Abstract: A manufacturing method includes a core portion forming step, a coating portion forming step, and a core portion removing step. The core portion forming step is a step of forming a core portion in a granular shape. The coating portion forming step is a step of forming a coating portion so as to cover the core portion. The coating portion removing step is a step of removing a part of the coating portion.

Abstract: A nanostructured material consisting essentially of boron. The material is in amorphous form and comprising aggregates of boron nanoparticles. A method of preparation thereof and the uses thereof.

Abstract: A process of methane catalytic conversion produces olefins, aromatics, and hydrogen under oxygen-free, continuous flowing conditions. Such a process has little coke deposition and realizes atom-economic conversion. Under the conditions encountered in a fixed bed reactor (i.e. reaction temperature: 750-1200° C.; reaction pressure: atmospheric pressure; the weight hourly space velocity of feed gas: 1000-30000 ml/g/h; and fixed bed), conversion of methane is 8-50%. The selectivity of olefins is 30-90%. And selectivity of aromatics is 10-70%. The catalyst for this methane conversion has a SiO2-based matrix having active species that are formed by confining dopant metal atoms in the lattice of the matrix.

Abstract: The present invention discloses a preparation method of an alumina supported cerium oxide powder material. A cerium organometallic precursor is effectively decomposed into CeO2 nanoparticles at 500-700° C. in an oxygen atmosphere condition by using a chemical vapor deposition method, and the CeO2 nanoparticles are evenly dispersed on an Al2O3 support. The decomposition of the CeO2 precursor is accelerated by changing experimental parameters of reaction between organic materials and oxygen, so as to control the size and microstructure of powder, thereby achieving the preparation and even dispersion of cerium oxide nanoparticles, and avoiding the problem of generation of toxic waste liquor during reaction. The method of the present invention is simple, has a short preparation period, and the cerium oxide nanoparticles prepared are evenly dispersed, can be used as catalytic materials and functional materials, and have a broad application prospect in multiple fields.

Abstract: Zn-promoted and/or Ga-promoted cracking catalysts, such as cracking catalysts comprising an MSE framework zeolite or an MFI framework zeolite can provide unexpectedly superior conversion of branched paraffins when used as part of a catalyst during reforming of a hydrocarbon fuel stream. The conversion and reforming of the hydrocarbon fuel stream can occur, for example, in an internal combustion engine. The conversion and reforming can allow for formation of higher octane compounds from the branched paraffins.

Abstract: A lean NOx trap catalyst and its use in an emission treatment system for internal combustion engines is disclosed. The lean NOx trap catalyst comprises a first layer and a second layer.

Abstract: A preparation method of an alumina-carbon nano tube composite powder material includes the steps of using an organometallic precursor as a raw material, using metal nanoparticles formed on the surface of the alumina powder as a catalyst, and simultaneously feeding a carbonaceous gas such as methane and acetylene, so as to grow a carbon nano tube in situ, and obtain an alumina-metal nanoparticle-carbon nano tube composite powder material through a chemical vapor deposition method under a temperature condition of 400 to 800° C. Through changing various parameters such as the weight of the organic raw material, the flow or constituent of reactant gases and reaction temperature, the decomposition of the organic raw material and the generation of the metal nanoparticles and the carbon nano tube are adjusted, and the size and the microstructure of the powder are controlled.

Abstract: The present invention relates to a honeycomb structure having promoter particles and a binder phase interposed between the promoter particles, and a method for manufacturing the same. The promoter particles contain at least first promoter particles made of a ceria-zirconia solid solution. The binder phase, in each of which a number of inorganic binder particles are aggregated with each other, with ?-alumina being a main component, contain one or two of Fe and Cr dissolved in ?-alumina. The honeycomb structure has a specific surface area at a ratio of 90% or more of after heating to before heating at a temperature of 1200° C.

Abstract: Described herein are materials and methods for improved catalytic oligomerization of an ethylene monomer and/or propylene monomer. The present disclosure teaches oligomerizing the ethylene monomer or propylene monomer to produce oligomers. Also described is a heterogeneous catalyst comprising sulfate modified nickel on titanium modified alumina and a surface modification with yttrium (Y) suitable for use in the disclosed oligomerization.

Abstract: The present invention relates to a catalyst for the dehydrogenation of hydrocarbons which is based on iron oxide and additionally comprises at least one potassium compound, at least one cerium compound, from 0.7 to 10% by weight of at least one manganese compound, calculated as Mn02, and from 10 to 200 ppm of at least one titanium compound, calculated as TiO2, and also to a process for the production thereof. Furthermore, the present invention relates to a process for the catalytic dehydrogenation of hydrocarbons using the catalyst of the invention.

Abstract: A method for recovering a catalyst, wherein a solution containing a reaction mixture obtained by performing a hydrogenation reaction in a presence of a catalyst containing a platinum group metal is brought into contact with a fiber membrane having a group containing an amino group or a thiol group on a surface, thereby recovering the platinum group metal included in the solution is provided.

Abstract: A process is presented for the management of sulfur on a catalyst. The catalyst is a dehydrogenation catalyst, and sulfur accumulates during the dehydrogenation process. Sulfur compounds are stripped from the spent catalyst and the catalyst is cooled before the regeneration process. The process includes controlling the amount of sulfur that needs to be removed from the catalyst before regeneration.

Abstract: A process is presented for the management of sulfur on a catalyst. The catalyst is a dehydrogenation catalyst, and sulfur accumulates during the dehydrogenation process. Sulfur compounds are stripped from the spent catalyst and the catalyst is cooled before the regeneration process. The process includes controlling the amount of sulfur that needs to be removed from the catalyst before regeneration.

Abstract: A supported catalyst and preparation method thereof, the catalyst comprising an organic polymer material carrier and Raney alloy particles supported on the organic polymer material carrier, wherein substantially all of the Raney alloy particles are partially embedded in the organic polymer material carrier. The catalyst can be used in hydrogenation, dehydrogenation, amination, dehalogenation or desulfuration reactions.

Abstract: A unique crystalline bis-ammonia transition metal molybdotungstate material has been developed. The material may be used as a hydroprocessing catalyst. The hydroprocessing may include hydrodenitrification, hydrodesulfurization, hydrodemetallation, hydrodearomatization, hydrodesilication, hydroisomerization, hydrotreating, hydrofining, and hydrocracking.

Abstract: A porous ceramic honeycomb body including a substrate of intersecting porous walls forming axial channels extending from a first end face to a second end face. An active portion of the walls include a zeolite catalyst disposed inside pores thereof and/or is comprised of an extruded zeolite and a three way catalyst (TWC) is disposed on wall surfaces of at least a portion of the active portion.

Abstract: A process for the production of para-xylene is presented. The process includes the isomerization of C8 aromatics to para-xylene utilizing a new catalyst. The new catalyst and designated as UZM-54 is represented by the empirical composition in the as synthesized and anhydrous basis expressed by the empirical formula of: Mmn+R1 r1p1+ R2 r2p2+ Al1-xExSiyOz where M is an alkali, alkaline earth, or rare earth metal such as sodium and/or potassium, R1 and R2 are organoammonium cation and E is a framework element such as gallium, iron, boron, or indium. UZM-54 are characterized by unique x-ray diffraction patterns, high meso surface area, low Si/Al ratios.

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 composition useful in oxidative desulphurization of gaseous hydrocarbons is described. It comprises a CuZnAl—O mixed oxide, and an H form of a zeolite. The mixed oxide can contain one or more metal oxide promoters. The H form of the zeolite can be desilicated, and can also contain one or more transition metals.

Abstract: Methods for producing supported catalysts containing a transition metal and a bound zeolite base are disclosed. These methods employ a step of washing the bound zeolite base in the presence of an alkali metal, prior to impregnating the bound zeolitic support with the transition metal. Alkali metals such as potassium and cesium may be used.

Abstract: The present invention relates to a hydroisomerization and cracking catalyst for preparing biological aviation kerosene from castor oil as well as a preparation method and an application thereof. The catalyst takes a Al-modified titanium silicate molecular sieve (TS-1) as a carrier, and takes NixW and NixMo as active components, wherein x is the atomic ratio of Ni to W or Ni to Mo, and x=5-10, wherein the mass of the active components accounts for 5-30% of the total mass of the catalyst; the molar ratio of Si:Ti in the Al-modified titanium silicate molecular sieve is 50-100, and the molar ratio of Si:Al is 50-100.

Abstract: Methods for regenerating a sulfur-contaminated catalyst are disclosed. Such methods may employ a step of washing the sulfur-contaminated catalyst with an aqueous solution containing an alkali metal, followed by contacting the washed catalyst with a halogen solution containing chlorine and fluorine.