Abstract: A method of preparing borosulfate materials avoids the need for fuming sulfuric acid, also known as oleum. Instead, B(OH)3 present in solution in concentrated sulfuric acid at 5% to 15% by weight is reacted with a cation source at 100-250° C. under dynamic vacuum while in connection with a receiving vessel comprising a desiccant and separate from the reaction vessel, thereby causing formation of a borosulfate material in the reaction vessel while eliminated water is collected in the receiving vessel.

Abstract: A multi-component inorganic capsule anchoring system can be used for chemical fastening of anchors, bolts, screw anchors, screw bolts, and post-installed reinforcing bars in mineral substrates. The multi-component inorganic capsule anchoring system contains a curable powdery ground-granulated blast-furnace slag-based component A, and an initiator component B in aqueous-phase for initiating the curing process. The powdery ground-granulated blast-furnace slag-based component A contains further silica dust. The component B contains an alkali- or alkaline earth-hydroxide, alkali- or alkaline earth-carbonate, or alkali- or alkaline earth-sulfate component.

Abstract: Disclosed is separation process of valuable metals from copper anode slime based on oxidation potential modulation, belonging to the technical field of industrial solid waste resource utilization. The differences in redox properties of different metal elements are used to precisely regulate the oxidation potential and acidity of the leaching solution by regulating the amount of oxidizing agent and acid added, so as to selectively and graded leaching and separating the copper (Cu), selenium (Se), tellurium (Te), and silver (Ag) metal elements, and the oxidants used are substances such as H2O2, O2 and O3.

Abstract: The present application pertains to processes for making calcium oxide and/or sulfuric acid from calcium sulfate. In some embodiments the processes comprise reacting a component comprising calcium sulfate with a second component comprising magnesium sulfite under conditions to form a solid comprising calcium sulfite and a solution comprising magnesium sulfate. Next, at least a portion of the solid comprising calcium sulfite is decomposed to form a second solid comprising calcium oxide, or calcium hydroxide, or cement, or clinker, or any combination thereof.

Abstract: This invention relates generally to a system and process for recovery of select minerals and lithium from a geothermal brine. The system and process are configured for the sequential recovery of zinc, manganese, and lithium from a Salton Sea Known Geothermal Resource Area brine. The system and process includes: 1) an impurity removal circuit; then 2) a continuous counter-current ion exchange (CCIX) circuit for selectively recovering lithium chloride from the brine flow and concentrating it using a CCIX unit; and then 3) a lithium chloride conversion circuit for converting lithium chloride to lithium carbonate or lithium hydroxide product.

Abstract: The present disclosure is directed to a coating composition including a graphene oxide and a solvent. At least one of a carboxyl group and an epoxide group of the graphene oxide is functionalized by an amine. The amine has an activation energy to an epoxide group of the graphene oxide of about ?3 kcal/mol to about 8 kcal/mol. A method of forming a stacked structure using the coating composition is provided. A method of manufacturing a display device using the coating composition is provided.

Abstract: Provided is a method for removing arsenic from copper smelting soot and comprehensive recovery of valuable metals. According to the method, a metal leaching synergist is prepared through thiol-ene click chemical reaction, which is capable of reacting more effectively with arsenic and metal impurities in the copper smelting soot due to its special chemical structure, thereby improving leaching efficiency; and the cage-like structure of the polysilsesquioxane provides excellent chemical stability, the removal rate of harmful substances in the copper smelting soot can be increased by using the synergist, environmental pollution is reduced, meanwhile, the recovery rate of metal resources is increased, and the requirements of green chemistry and sustainable development are met. The present disclosure realizes the centralized management of As and also realizes the step-by-step recovery of valuable metals such as Cu, Zn, Pb, Bi, and In.

Abstract: A vehicle surface treatment composition includes a colloidal inorganic oxide dispersion or a soluble silicate amenable to application to both porous and semi-porous vehicle hard surfaces to provide a multi-surface protective barrier that imparts water repellency and weathering protection properties to the vehicle finish. The composition provides a hard surface cleaning and forms a coating to the applied surface. The compositions provide treated surface properties that include keeping clean, scratch/mar defense, bug repellency, UV protection, and weathering defense. The compositions create treated surfaces that are highly smooth and lubricious which provide enhanced protection, while achieving a high luster finish with a streak free appearance. The composition is readily applied through resort to a conventional trigger spray application, propellant aerosol, or a sponge or cloth for wipe application onto the vehicle surface.

Abstract: The invention provides an automated method for isolating a targeted isotope, the method having the steps of supplying a dissolved uranium targets into a first reaction environment; precipitating non-targeted isotope within the first reaction environment transferring liquid phase targeted isotope to a second reaction environment; precipitating the liquid phase targeted isotope in the second reaction environment; dissolving the precipitated targeted isotope; transferring the dissolved targeted isotope to a third reaction environment; and precipitating non-targeted isotope (i.e., iodine), such that the targeted isotope remains in the solution. Also provided is an automated system for isolating isotopes, the system having a plurality of reaction environments adapted to pneumatically receive and disgorge reactants and products via remotely actuated valves positioned between each of the reaction environments.

Abstract: Described herein are technologies for concentrating rare-earth elements from a heavy fraction of grit in gangue produced in kaolin mining. In some examples, grit is separated as a non-clay fraction of gangue produced in a kaolin mining operation. The grit is separated into a heavy mineral grit sub-fraction and a light mineral grit sub-fraction. Rare-earth elements, particularly heavy rare-earth elements, are thereafter extracted from the heavy mineral grit sub-fraction using various extraction technologies.

Abstract: A method and apparatus of preparing lithium compound(s) from lithium-containing mineral includes a) a leaching step, wherein the lithium-containing mineral is leached in aqueous leach solution containing alkaline carbonate, for liberating lithium and phosphate(s) from the lithium-containing mineral, thus obtaining leach slurry containing lithium carbonate and phosphate(s) leach slurry, b) a carbonization step, wherein the leach slurry containing lithium carbonate and phosphate(s), obtained from the leaching step, is reacted with an alkali earth metal compound in the presence of CO2 for obtaining a carbonated slurry containing lithium hydrogen carbonate, and for precipitating phosphate(s) contained in the leach slurry as insoluble phosphate compound(s), c) a solid-liquid separation step, wherein the carbonated slurry obtained from carbonization step is subjected to solid-liquid separation wherein the undissolved mineral and phosphate compound(s) are separated as solids that can be recovered or discarded, there

Abstract: Provided are processes for extracting nickel and lithium from a Ni2+/Li+ solution. The process for extracting nickel and lithium includes providing a Ni2+/Li+ solution comprising an amount of lithium and an amount of nickel, treating the Ni2+/Li+ solution with an alkaline agent to adjust the pH of the Ni2+/Li+ solution to between about 1.0 to about 10.0, and treating the Ni2+/Li+ solution with a nickel selective extractant, the nickel selective extractant suitable to extract nickel from the Ni2+/Li+ solution at said pH to thereby produce a Li+ solution with less than 1000 parts per million Ni2+. Once complete, the process provides for recoverable nickel and/or lithium that may be recycled into batteries or sold for other uses.

Abstract: A method for producing an aqueous solution containing nickel, cobalt and manganese, includes: a leaching process including a pressure-leaching process of leaching a raw material under pressure to form a leachate containing nickel, cobalt, manganese and impurities; an impurity removal process of removing the impurities from the leachate; a target substance precipitation process of precipitating a mixed hydroxide precipitate containing nickel, cobalt and manganese by introducing a neutralizing agent into a filtrate from which the impurities are removed; and a dissolution process. The pressure-leaching process includes a first-stage pressure-leaching process and a second-stage pressure-leaching process of pressure-leaching a residue of the first-stage pressure-leaching process with an acidity higher than an acidity in the first-stage pressure-leaching process.

Abstract: The present disclosure provides systems and methods for fast molten salt reactor fuel-salt preparation. In one implementation, the method may comprise providing fuel assemblies having fuel pellets, removing the fuel pellets and spent fuel constituents from the fuel assemblies, granulating the removed fuel pellets or process feed to a chlorination process, processing the granular spent fuel salt into chloride salt by ultimate reduction and chlorination of the uranium and associated fuel constituents chloride salt solution, enriching the granular spent fuel salt, chlorinating the enriched granular spent fuel salt to yield molten chloride salt fuel, analyzing, adjusting, and certifying the molten chloride salt fuel for end use in a molten salt reactor, pumping the molten chloride salt fuel and cooling the molten chloride salt fuel, and milling the solidified molten chloride salt fuel to predetermined specifications.

Abstract: Provide is a rubber composition for a tire that improves mechanical properties beyond conventional levels. The rubber composition for a tire according to an embodiment of the present invention contains from 1 to 50 parts by mass of oxidized cellulose nanofibers blended in 100 parts by mass of diene rubber containing 5% by mass or greater of modified diene rubber having 0.1% by mol or greater of a polar group.

Abstract: A catalytic structure has a plurality of high-entropy alloy (HEA) nanoparticles. Each HEA nanoparticle is composed of a homogeneous mixture of elements of cobalt (Co), molybdenum (Mo), and at least two transition metal elements. For example, in some embodiments, each HEA nanoparticle is a quinary mixture of Co, Mo, iron (Fe), nickel (Ni), and copper (Cu). The homogeneous mixture in each HEA nanoparticle forms a single solid-solution phase. The catalytic structure is used to catalyze a chemical reaction, for example, ammonia decomposition or ammonia synthesis. Methods for forming the catalytic structure are also disclosed.

Abstract: A carbon material for use as a catalyst carrier for a polymer electrolyte fuel cell which is a porous carbon material and satisfies at the same time (1) the content of a crystallized material is 1.6 or less, (2) the BET specific surface area obtained by a BET analysis of a nitrogen gas adsorption isotherm is from 400 to 1500 m2/g, (3) the cumulative pore volume V2-10 with respect to a pore diameter of from 2 to 10 nm obtained by an analysis of a nitrogen gas adsorption isotherm using the Dollimore-Heal method is from 0.4 to 1.5 mL/g, and (4) the nitrogen gas adsorption amount Vmacro between a relative pressure of 0.95 and 0.99 in a nitrogen gas adsorption isotherm is from 300 to 1200 cc (STP)/g, and the method of producing the same.

Abstract: According to embodiments, a method of producing a catalyst composition may include forming a slurry including an initial zeolite material, a surfactant, silica, and metal precursors, wherein the metal precursors contain a nickel-containing compound and a silver-containing compound, extruding the slurry to produce an extrudate, drying and calcining the extrudate to form a dried and calcined extrudate, hydrothermally treating the dried and calcined extrudate to form a hydrothermally-treated extrudate, and drying and calcining the hydrothermally-treated extrudate to produce the catalyst composition, wherein the catalyst composition includes zeolite, one or more oxides of nickel, and one or more oxides of silver.

Abstract: A preparation method of an SSZ-13 zeolite membrane is provided, and the SSZ-13 zeolite membrane belongs to the technical field of zeolite membranes. The problem that the SSZ-13 zeolite membranes synthesized in the art have a poor quality and a large thickness is solved. A FAU-type zeolite is used as a raw material, and transformed into an SSZ-13 zeolite with a particle size of 210 nm through intergranular transformation, with a mass yield of 91.2%. A crystal seed prepared by the preparation method has a small particle size and a small thickness.

Abstract: A copper/molybdenum separation processor is provide featuring a slurry/media mixture stage configured to receive a conditioned pulp containing hydrophobic molybdenite and hydrophilic copper, iron and other minerals that is conditioned with sodium hydrosulfide together with an engineered polymeric hydrophobic media, and provide a slurry/media mixture; and a slurry/media separation stage configured to receive the slurry/media mixture, and provide a slurry product having a copper concentrate and a polymerized hydrophobic media product having a molybdenum concentrate that are separately directed for further processing. The slurry/media mixture stage include a molybdenum loading stage configured to contact the conditioned pulp with the engineered polymeric hydrophobic media in an agitated reaction chamber, and load the hydrophobic molybdenite on the engineered polymeric hydrophobic media.