Abstract: Methods of making robust bijels include dispersing metal oxide precursors and/or metal salts into at least one phase of a bijel and hydrolyzing and condensing the metal oxide precursors and/or metal salts in a sol-gel reaction to form sintered bridges between interfacially jammed surface-active nanoparticles. The methods can be used with any bijels, including those produced during solvent transfer-induced phase separation (STRIPS) methods and other methods. A robust bijel includes chemically sintered bridges between the interfacially jammed surface-active nanoparticles. Methods of making nanocatalyst-functionalized sintered bijels include adsorbing metal salts to a surface of sintered interfacially jammed nanoparticles of bijels, and reducing the metal precursors on the surface of the sintered nanoparticles. Nanocatalyst-functionalized sintered bijels include catalytically active metal or metal oxide nanocatalysts on a surface of the sintered interfacially jammed surface-active nanoparticles.

Abstract: Inorganic coatings that may be used to coat and protect steel are disclosed. The protective inorganic coatings include a liquid composition portion comprising water, alkali metal oxide components and a silicate-containing component. The coatings also include a powder composition portion comprising microspheres, metal oxide powder and optional microfibers. When applied to steel substrates, the coatings provide chemical and physical protection.

Abstract: A process for the manufacturing of 3D reduced graphene oxide/Fe2O3 material includes the following steps: (i) putting in contact a graphene oxide (GO) water dispersion with an aqueous solution of iron(II) sulfate; (ii) hydrothermal treatment; and (iii) freezing the reaction product obtained in step (ii) at a temperature ??5° C.; and (iv) lyophilisation. A 3D reduced graphene oxide/Fe2O3 material is obtainable by the process and further relates to electrodes for CDI devices having the material. A method for removing ions from a fluid, like saline water, using the capacitive deionization device includes applying a voltage to the electrodes while supplying the fluid into the capacitive deionization device.

Abstract: In various embodiments, single-crystal aluminum nitride boules and substrates are highly visibly transparent and have low Urbach energies and/or absorption coefficients at deep-ultraviolet wavelengths. The single-crystal aluminum nitride may function as a platform for the fabrication of light-emitting devices such as light-emitting diodes and lasers.

Abstract: The present invention provides a particularly advantageous form of alkaline earth metal hydroxystannate and alkaline earth metal stannate exhibiting a BET specific surface area of from 20 to 200 m2/g. A method of producing such particulate material and evidence of its benefits in use such as in at a reduction in a polymer sample at elevated temperature is also disclosed.

Abstract: A catalyst, a preparation method therefor, an electrode containing the catalyst, a membrane-electrode assembly, and a fuel cell are disclosed. The catalyst contains a support; metal particles supported by the support; and a coating layer located on the metal particles, and includes any one selected from the group consisting of phthalocyanine, M-phthalocyanine (wherein M is a transition metal) and a mixture thereof. The catalyst has improved durability since a coating layer is formed on the surface of a commercial catalyst or a conventional catalyst through a relatively easy method without separate treatment. A carbon coating layer formed by post-treating a catalyst including the coating layer further improves durability. Material transfer ability and performance are also improved by a carbon nanofiber or a carbon nanotube generated during post-treatment.

Abstract: The present disclosure discloses a method for growing a crystal in oxygen atmosphere. The method includes compensating a weight of a reactant, introducing a flowing gas, improving a volume ratio of oxygen during a cooling process, providing a heater in a temperature field, and optimizing parameters. According to the method, cracking and component deviation of the crystal during a crystal growth process, and without oxygen free vacancy can be solved. The method for growing the crystal has excellent repeatability and crystal performance consistency.

Abstract: Presented is a catalyst composition having exceptional properties for converting sulfur, sulfur compounds, and carbon monoxide contained in gas streams by catalyzed hydrolysis, hydrogenation and water-gas shift reactions. The catalyst comprises underbedded molybdenum and cobalt with an overlayer of molybdenum and cobalt. These metals are present in the catalyst within certain concentration ranges and relative weight ratios. The underbedded metals are present in the catalyst within a specified range relative to the overlayer and total metals. The underbedded metals are formed by co-mulling an inorganic oxide with the catalytically active metals of molybdenum and cobalt. The co-mulled mixture is calcined and then impregnated with overlaid molybdenum and cobalt.

Abstract: The present invention discloses a method for rapidly preparing a Prussian blue analogue with a monoclinic crystal structure. The Prussian blue analogue with a monoclinic crystal structure has a chemical formula of NaxM[Fe(CN)6]y·zH2O, where M=Mn or Fe, 1.5<×<2, and 0.5<y<1. In this method, a mixture of sodium ferrocyanide and sodium chloride is adopted as a solution A, and a solution of manganese salt or iron salt in water is adopted as a solution B; the solutions A and B are continuously and rapidly mixed by a micromixer, and the precipitation reaction is conducted to obtain a nano-precursor slurry; and the nano-precursor slurry is aged at 80° C. to 160° C. for 3 min to 2 h to obtain a Prussian blue analogue with a monoclinic crystal structure that has a particle diameter of 200 nm to 2,000 nm.

Abstract: The present invention provides processes for preparing metal oxide semiconductor nanomaterials.

Abstract: A method for the synthesis of carbon nanotubes from natural rubber, including providing a first material, the first material may include natural rubber or derivatives thereof, thermally decomposing the first material at a first temperature into an intermediate material, contacting the intermediate material with a catalyst, treating the intermediate material in contact with the catalyst at a second temperature, for forming carbon nanotubes. Adjusting an average characteristic of resulting nanotubes, including carrying out the synthesis method as a reference method and for decreasing the average diameter of the nanotube: decreasing the second temperature and/or decreasing the reaction time and/or increasing the concentration of H2 in the forming gas in relation to the reference method. Or, for increasing the average diameter of the nanotube: increasing the second temperature and/or increasing the reaction time and/or decreasing the concentration of H2 in the forming gas in relation to the reference method.

Abstract: The reaction rate of hydrocarbon pyrolysis can be increased to produce solid carbon and hydrogen by the use of molten materials which have catalytic functionality to increase the rate of reaction and physical properties that facilitate the formation and contamination-free separation of the solid carbon. Processes, materials, reactor configurations, and conditions are disclosed whereby methane and other hydrocarbons can be decomposed at high reaction rates into hydrogen gas and carbon products without any carbon oxides in a single reaction step. The process also makes use of specific properties of selected materials with unique solubilities and/or wettability of products into (and/or by) the molten phase to facilitate generation of purified products and increased conversion in more general reactions.

Abstract: A solid ionically conductive composition (e.g., nanoparticles of less than 1 micron or a continuous film) comprising at least one element selected from alkali metal, alkaline earth metal, aluminum, zinc, copper, and silver in combination with at least two elements selected from oxygen, sulfur, silicon, phosphorus, nitrogen, boron, gallium, indium, tin, germanium, arsenic, antimony, bismuth, transition metals, and lanthanides. Also described is a battery comprising an anode, a cathode, and a solid electrolyte (corresponding to the above ionically conductive composition) in contact with or as part of the anode and/or cathode. Further described is a thermal (e.g., plasma-based) method of producing the ionically conductive composition. Further described is a method for using an additive manufacturing (AM) process to produce an object constructed of the ionically conductive composition by use of particles of the ionically conductive composition as a feed material in the AM process.

Abstract: Methods for preparing molybdenum-based catalyst for epoxidation reactions using MPG sourced from a propylene oxide/styrene monomer (POSM) production process are described. Streams exiting from the POSM reactor are combined and separated to isolate an aqueous-based, MPG-containing purge stream from other recoverable byproducts of the POSM process. This MPG-containing purge stream is then used as is in the catalyst preparation of molybdenum-based catalyst for epoxidation. Alternatively, the MPG-containing purge stream can undergo additional purification treatments before being utilized in the catalyst preparation.

Abstract: The present disclosure relates to a catalyst for preparing 1,2-pentanediol from furfural and/or furfuryl alcohol, and more particularly to a catalyst, which is configured such that a catalytically active metal containing both at least one transition metal and tin (Sn) is supported on a basic support and is capable of increasing reaction selectivity for 1,2-pentanediol, and a method of preparing 1,2-pentanediol using the same.

Abstract: A process of manufacture of a solid catalyst made of a support coated with a thin catalytic layer and a process for eliminating gaseous and/or particulate pollutants in an exhaust gas. The process of manufacture includes preparing a solution A by dissolving alkoxide and/or chloride precursors of at least one metal selected from Al, Si, Ti, Zr, Fe, Zn, Nb, V and Ce in a solvent S1, preparing a solution B containing a surfactant, an organic acid, and/or hydrochloric acid (HCl) in a solvent S2, mixing solution A and solution B together, thereby obtaining a washcoat solution C, and dip-coating, drying, and calcinating the support into washcoat solution C. The processes provide for elimination of volatile organic compounds (VOCs), CO, and/or particulate pollutants in an exhaust gas.

Abstract: Methods for conditioning an ethylene epoxidation catalyst are provided. The conditioning methods comprise contacting an ethylene epoxidation catalyst comprising a carrier, having silver and a rhenium promoter deposited thereon, with a conditioning feed gas comprising oxygen for a period of time of at least 2 hours at a temperature that is above 180° C. and at most 250° C., wherein the contacting of the ethylene epoxidation catalyst with the conditioning feed gas occurs in an epoxidation reactor and in the absence of ethylene. Associated methods for the epoxidation of ethylene are also provided.

Abstract: A method of removing fluoride ion from waste liquid is provided, which includes providing a calcium source and a plurality of ceramic particles to a waste liquid containing fluoride ion for forming a plurality of calcium fluoride layers wrapping the ceramic particles. The calcium fluoride layers are connected to form a calcium fluoride bulk. The ceramic particles are embedded in the calcium fluoride bulk. The ceramic particles and the calcium fluoride bulk have a weight ratio of 1:4 to 1:20.

Abstract: A multifunctional self-cleaning surface layer and methods of preparing the multifunctional self-cleaning surface layer are provided. The multifunctional self-cleaning surface layer includes an inorganic matrix including silicon and oxygen; a plurality of photocatalytic active particles distributed within and bonded to the inorganic matrix; and a plurality of nanopores defined within the inorganic matrix in regions corresponding to bonds between the plurality of photocatalytic active particles and the inorganic matrix. Water molecules may be disposed within at least a portion of the plurality of nanopores. In the presence of water and electromagnetic radiation, the plurality of photocatalytic active particles may facilitate a decomposition reaction of any oil or organic residue on the multifunctional self-cleaning surface layer.

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.