Abstract: Methods for preventing or reducing the formation of scale in a wet-process phosphoric acid production process by intermixing a scale inhibiting reagent at one or more step of the phosphoric acid production process in an amount sufficient to prevent or reduce scale are provided.

Abstract: Systems and methods for producing ammonia and/or ammonia products. The ammonia and/or ammonia products can be produced by compressing a gas mixture comprising nitrogen, hydrogen, methane, and argon to produce a compressed gas mixture having a pressure of from about 1,000 kPa (130 psig) to about 10,400 kPa (1,495 psig). All or a portion of the compressed gas mixture can be selectively separated at cryogenic conditions to produce a first gas comprising nitrogen and hydrogen, and a second gas comprising methane, argon, residual hydrogen and nitrogen. At least a portion of the first gas can be reacted at conditions sufficient to produce an ammonia product.

Abstract: A process for producing KNO3 from polyhalite to is disclosed. In a preferred embodiment, the process comprises steps of (a) contacting polyhalite with HNO3; (b) adding Ca(OH)2 to the solution, thereby precipitating as CaSO4 at least part of the sulfate present in said solution; (c) precipitating as Mg(OH)2 at least part of the Mg2+ remaining in said solution by further addition of Ca(OH)2 to the remaining solution; (d) concentrating the solution, thereby precipitating as a sulfate compound at least part of the sulfate remaining in solution; (e) separating at least part of the NaCl from the solution remaining; and (f) crystallizing as solid KNO3 at least part of the K+ and NO3-contained in the solution. The process enables direct conversion of polyhalite to KNO3 of purity exceeding 98.5% and that is essentially free of magnesium and sulfate impurities.

Abstract: A method of preparing purified barium nitrate includes precipitating barium nitrate crystals from a solution, and washing the barium nitrate crystals with an aqueous solution including at least 10 wt % nitric acid.

Abstract: A method and device for producing polyphosphoric acid burns a fuel in combustion air in a combustion chamber, sprays a spray fluid comprising substantially pure orthophosphoric acid and undertakes polymerization-condensation of the pure orthophosphoric acid. A polyphosphoric acid in the form of an acid mist accompanied by formation of gases which mix with combustion gases resulting from burning of the fuel is formed to reach a predetermined temperature, wherein the mixture causes sudden lowering of combustion gas temperature. The acid mix is separated from the gas mixture and the polyphosphoric acid is collected at a bottom of the combustion chamber and the gas mixture is outputted via a lower part of the combustion chamber separate from the collection of polyphosphoric acid.

Abstract: A process comprises (a) combining (1) at least one base and (2) at least one metal carboxylate salt comprising (i) a metal cation selected from metal cations that form amphoteric metal oxides or oxyhydroxides and (ii) a lactate or thiolactate anion, or metal carboxylate salt precursors comprising (i) at least one metal salt comprising the metal cation and a non-interfering anion and (ii) lactic or thiolactic acid, a lactate or thiolactate salt of a non-interfering, non-metal cation, or a mixture thereof; and (b) allowing the base and the metal carboxylate salt or metal carboxylate salt precursors to react.

Abstract: The present invention is directed to methods comprising adding NH3 to a SO2F2 solution to directly form a FSO2NH2 and/or a salt of [FSO2NH]?, optionally quenching any unreacted NH3 present in the resulting mixture, and isolating the product from the resulting mixture.

Abstract: The invention relates to a method for generating nitric oxide, in particular for therapeutic applications, which comprises the steps of: guiding a process gas into a reaction chamber 3, wherein the process gas comprises nitrogen and oxygen, heating the process gas to a temperature which is sufficiently high to enable a reaction of oxygen and nitrogen to form nitric oxide, thereby forming a gas which comprises nitric oxide, and extracting the nitric oxide comprising gas from the reaction chamber 3, wherein oxygen is present in the process gas in the reaction chamber in an amount of <5 vol-%.

Abstract: An embodiment of a method for recovering nitric acid from acid pickling solution includes introducing a treating material comprising at least one chemical into a pickling solution comprising free nitric acid. The treating material reacts with at least a portion of the free nitric acid in the pickling solution and produces NOx. A gas stream comprising at least a portion of the NOx is contacted with ozone, thereby forming oxidation products including nitrogen sesquioxide and nitrogen pentoxide. At least a portion of the nitrogen sesquioxide and nitrogen pentoxide is contacted with water, thereby forming nitric acid, and at least a portion of the nitric acid is collected.

Abstract: Elemental boron with a boron content of at least 96.8% by weight, an oxygen content of at most 1.6% by weight, a nitrogen content of at most 0.2% by weight, a crystallinity of 30% by weight or less, and a particle size distribution with a d100 value of 9 ?m or less.

Abstract: Methods and systems for treating a gas stream comprising NOx are disclosed. In one embodiment of the method, the gas stream comprising NOx is reacted with ozone to form oxidation products including nitrogen sesquioxide and nitrogen pentoxide. At least a portion of the nitrogen sesquioxide and nitrogen pentoxide is reacted with water to form nitric acid, and a solubilized form of the nitric acid is collected and may be reused or otherwise utilized. Systems for conducting the method also are disclosed.

Abstract: A method for the manufacture of a III-V compound in the form of nanoparticles, such as those used in semi-conductors. The reaction proceeds at atmospheric pressure in a reaction solution by the reaction of a III compound source and a V compound source. The reaction proceeds in solvent of high boiling point. The solvent contains a stabilizer and a base. The manufactured III-V compound is precipitated from the reaction solution, isolated, purified and analyzed.

Abstract: Provided is a method for preparing high-purity elemental phosphorus capable of simultaneously reducing both arsenic and antimony from crude white phosphorus containing a great amount of arsenic and antimony as impurities. Provided is a method for preparing high-purity elemental phosphorus, the method including bringing liquid crude white phosphorus into contact with an iodic acid-containing compound selected from iodic acid and iodates in an aqueous solvent in the presence of a chelating agent, wherein the chelating agent is selected from polyvalent carboxylic acids, polyvalent carboxylates, phosphonic acid and phosphonates.

Abstract: The present invention relates to a synthetic method for producing a per-hydroxylated icosahedral boron compound via catalytic hydroxylation of icosahedral boron compound using a soft electrophile.

Abstract: A phosphorous pentoxide producing method includes forming a reducing kiln bed using feed agglomerates containing a lignin sulfonate both inside the agglomerates and coating a surface of individual agglomerates. Freeboard particulates are generated from the agglomerates, an amount of particulates generated being less than would occur in the method with no lignin sulfonate. Kiln off gas is generated and phosphorous pentoxide is collected from the kiln off gas. The kiln discharges a residue containing processed agglomerates, less than 20% of the agglomerates' phosphate input to the kiln remaining in the residue. The percentage of input phosphate that remains in the residue is less than would occur in the method with no lignin sulfonate. The method may include forming green agglomerates. Controlling a drying rate of the green agglomerates may wick some of the lignin sulfonate onto the surface of individual drying agglomerates without adhering the agglomerates together.

Abstract: Gas distribution units of fluidized bed reactors are configured to direct thermally decomposable compounds to the center portion of the reactor and away from the reactor wall to prevent deposition of material on the reactor wall and process for producing polycrystalline silicon product in a reactor that reduce the amount of silicon which deposits on the reactor wall.

Abstract: The invention provides a method for producing hydrogen bis(fluorosulfonyl)imide (HFSI) by reacting hydrogen bis(halosulfonyl)imide (HXSI) with hydrogen fluoride, where each X is independently a nonfluoro-halide, such as Cl, Br, or I.

Abstract: A method for producing phosphates and/or compounds containing phosphates is provided, in particular alkaline-earth phosphates, alkaline-earth silicophosphates, and alkaline-earth oxides, comprising the following steps: (a) heating bones and/or fish bones or a composition of said components in a pyrolysis process in the absence of oxygen and under reductive conditions at temperatures between 500 and 1100° C., wherein among other things high-energy gases, vapors, and carbon are produced, (b) subsequently combusting the carbon produced in step (a) under oxidative conditions in an oxidation step, wherein an inorganic radical of alkaline-earth carbonates, alkaline-earth oxides, and alkaline-earth phosphates is produced.

Abstract: Provided herein are methods of synthesizing large-pore periodic mesoporous quartz. Using the methods herein, large-pore periodic mesoporous quartz has been synthesized at a lower pressure and a temperature than in any previous mesoporous crystalline method, yielding a unique mesoporous article having crystalline pore walls. For example, the methods involve modified nanocasting methods using a mesoporous starting material comprising silica, carbon as a an infiltrating pore filler, followed by application of pressure and heat sufficient to crystallize silica in the infiltrated starting material to form a mesoporous crystalline article having crystalline pore walls therein, and useful in many applications, including as a catalyst.

Abstract: A composition for binding environmentally-harmful substances in solid or semi-liquid state contains caustic magnesium oxide, non-ferrous metal salts as a hardener, non-ferrous metal oxides catalyzing formation of radial crystalline structures, and optionally water and other additives. A method of stabilization of environmentally-harmful substances binds these substances in the solid state or semi-liquid state in the composition containing caustic magnesium oxide, wherein the environmentally-harmful substances are supplemented by the composition containing caustic magnesium oxide, non-ferrous metal salts as hardener, non-ferrous metal oxides catalyzing formation of radial crystalline structures, and optionally water and other additives. A form of paste is obtained, followed by leaving the mixture for solidification and stabilization of the product.