A system and method for production of ammonia are presented. The system includes a reactor adapted to receive therein through a first input of the reactor sulfate ammonia and a reacting agent through a second input of the reactor, wherein the reactor is heated to a temperature not to exceed a predetermined temperature to create a chemical reaction between a sulfate ammonia and the reacting agent; and a purifier adapted to accept ammonia from the reactor and perform a purification process to purify the ammonia to a predetermined degree of purification.

Disclosed is a method for preparing ammonia gas through a reaction between an ammonium salt and a silicate. An aqueous solution of the ammonium salt in the form of atomized droplets is contacted with a silicate at a high temperature for a reaction to generate ammonia gas and a solid substance. The silicate can be solid particles, and forms a bed. The generated ammonia gas is collected, the solid substance is extracted, part of the same solid substance is mixed with a fresh silicate solid particle, and the mixture continuously reacts with the atomized droplets of the aqueous solution of the ammonium salt.

There is disclosed a cyclic process for producing taurine from monoethanolamine comprising the steps of: (a) reacting monoethanolamine with ammonium sulfate in the recycling mother liquor to yield monoethanolamine sulfate; (b) reacting the monoethanolamine sulfate with sulfuric acid to form 2-aminoethyl hydrogen sulfate ester; (c) subjecting the 2-aminoethyl hydrogen sulfate ester to a sulfonation reaction with ammonium sulfite to yield taurine and ammonium sulfate; (d) separating the taurine and the ammonium sulfate by means of solid-liquid separation; (e) removing the excess ammonium sulfite from the mother liquor to obtain an aqueous solution comprised of ammonium sulfate and (f) returning the aqueous solution to step (a) to complete the cyclic process.

A process for treating an ammonium fluorosulfate byproduct includes providing an ammonium fluorosulfate byproduct including primarily ammonium fluorosulfate and lesser amounts of fluorosulfonic acid and bis(fluorosulfonyl) imide, mixing the ammonium fluorosulfate byproduct with water, reacting the mixture of the ammonium fluorosulfate byproduct and the water at a hydrolysis reaction temperature to hydrolyze the ammonium fluorosulfate, the fluorosulfonic acid and the bis(fluorosulfonyl) imide to form ammonium bisulfate and aqueous hydrogen fluoride; and separating the ammonium bisulfate from the aqueous hydrogen fluoride.

A process for treating an ammonium fluorosulfate byproduct includes providing an ammonium fluorosulfate byproduct including primarily ammonium fluorosulfate and lesser amounts of fluorosulfonic acid and bis(fluorosulfonyl) imide, mixing the ammonium fluorosulfate byproduct with water, reacting the mixture of the ammonium fluorosulfate byproduct and the water at a hydrolysis reaction temperature to hydrolyze the ammonium fluorosulfate, the fluorosulfonic acid and the bis(fluorosulfonyl) imide to form ammonium bisulfate and aqueous hydrogen fluoride; and separating the ammonium bisulfate from the aqueous hydrogen fluoride.

Digestion of impure alumina with sulfuric acid dissolves all constituents except silica. Resulting sulfates, produced from contaminants in the impure alumina, remain in solution at approximately 90 C. Hot filtration separates silica. Solution flow over metallic iron reduces ferric sulfate to ferrous sulfate. Controlled ammonia addition promotes hydrolysis and precipitation of hydrated titania from titanyl sulfate that is removed by filtration. Addition of ammonium sulfate forms ferrous ammonium sulfate and ammonium aluminum sulfate solutions. Alum is preferentially separated by crystallization. Addition of ammonium bicarbonate to ammonium alum solution precipitates ammonium aluminum carbonate which may be heated to produce alumina, ammonia, and carbon dioxide. The remaining iron rich liquor also contains magnesium sulfate. Addition of oxalic acid generates insoluble ferrous oxalate which is thermally decomposed to ferrous oxide. Carbon monoxide reduces the ferrous oxide to metallic iron. Further oxalic acid addition precipitates magnesium oxalate which is thermally decomposed to magnesium oxide.

Digestion of impure alumina with sulfuric acid dissolves all constituents except silica. The resulting sulfatesaluminum sulfate, ferric sulfate, titanyl sulfate, and magnesium sulfate for alumina contaminated with iron-, titanium-, and/or magnesium-containing speciesremain in solution at approximately 90 C. Hot filtration separates silica. Solution flow over metallic iron reduces ferric sulfate to ferrous sulfate. Controlled ammonia addition promotes hydrolysis and precipitation of hydrated titania from titanyl sulfate that is removed by filtration. Addition of ammonium sulfate forms ferrous ammonium sulfate and ammonium aluminum sulfate solutions. Alum is preferentially separated by crystallization. Addition of ammonium bicarbonate to an ammonium alum solution precipitates ammonium aluminum carbonate which may be heated to produce alumina, ammonia, and carbon dioxide. The remaining iron rich liquor also contains magnesium sulfate. The addition of oxalic acid generates insoluble ferrous oxalate which is thermally decomposed to ferrous oxide and carbon monoxide which is used to reduce the ferrous oxide to metallic iron. Further oxalic acid addition precipitates magnesium oxalate which is thermally decomposed to magnesium oxide.

Provided is a method for producing nickel powder from a nickel ammine sulfate complex solution, comprising treatment steps of: (1) a seed crystal production step of producing nickel powder having an average particle size of 0.1 to 5 m; (2) a seed crystal addition step of adding the nickel powder obtained in the step (1) as seed crystals to form a mixed slurry; (3) a reduction step of forming a reduced slurry containing nickel powder formed by precipitation of a nickel component in the mixed slurry on the seed crystals; and (4) a growth step of performing solid-liquid separation to separate and recover the nickel powder as a solid phase component and then blowing hydrogen gas into a solution prepared by adding the nickel ammine sulfate complex solution to the recovered nickel powder to grow the nickel powder to form high purity nickel powder.

The invention relates to the electrodialytic production of ammonia and sulfuric acid from ammonium-sulfate-rich (waste) waters. An object of said invention was to provide a process for recovering ammonia and sulfuric acid from waters containing ammonium sulfate in high concentrations. The process should be practicable on an industrial scale and have good energy efficiency. This problem is solved by a combination of electrodialysis and water electrolysis. It results in ammonium sulfate being split back into ammonia and sulfuric acid. Unlike conventional three-chamber processes, the process of the invention employs a cell having only two compartments, which can however be multiply parallelized within the stack. This type of scale-up is much more cost-effective than connecting multiple cells in parallel.

Provided is a method for producing nickel powder from a nickel ammine sulfate complex solution, comprising treatment steps of: (1) a seed crystal production step of producing nickel powder having an average particle size of 0.1 to 5 m; (2) a seed crystal addition step of adding the nickel powder obtained in the step (1) as seed crystals to form a mixed slurry; (3) a reduction step of forming a reduced slurry containing nickel powder formed by precipitation of a nickel component in the mixed slurry on the seed crystals; and (4) a growth step of performing solid-liquid separation to separate and recover the nickel powder as a solid phase component and then blowing hydrogen gas into a solution prepared by adding the nickel ammine sulfate complex solution to the recovered nickel powder to grow the nickel powder to form high purity nickel powder.