The present invention provides a process for producing high purity hydromagnesite from a source of magnesium chloride. The process involves preparation of a magnesium chloride brine of a specific concentration and reacting with sodium carbonate, while maintaining the reaction at a specific temperature range to form a hydromagnesite precipitate. The product can be calcined to generate high purity magnesium oxide compounds.

The present invention provides a process for producing high purity hydromagnesite from a source of magnesium chloride. The process involves preparation of a magnesium chloride brine of a specific concentration, which is ammoniated at a specific temperature range, followed by carbonation, while maintaining the reaction at a specific temperature range to form a hydromagnesite precipitate. The product can be calcined to generate high purity magnesium oxide compounds.

The present invention provides a process for producing high purity hydromagnesite from a source of magnesium chloride. The process involves preparation of a magnesium chloride brine of a specific concentration, which is ammoniated at a specific temperature range, followed by carbonation, while maintaining the reaction at a specific temperature range to form a hydromagnesite precipitate. The product can be calcined to generate high purity magnesium oxide compounds.

Disclosed is a method for recovering magnesium from by-products generated in an electrolytic chlorine generation system. According to one aspect of the present disclosure, there is provided a method for recovering magnesium from by-products generated in an electrolytic chlorine generation system, the method including: receiving and drying the by-products in a preset first environment; and calcining the dried by-products in a preset second environment.

Disclosed is a method for recovering magnesium from by-products generated in an electrolytic chlorine generation system. According to one aspect of the present disclosure, there is provided a method for recovering magnesium from by-products generated in an electrolytic chlorine generation system, the method including: receiving and drying the by-products in a preset first environment; and calcining the dried by-products in a preset second environment.

A process and apparatus for manufacture of oxide products for use as biocide, chemical detoxifying, and catalytic support products, from caustic calcined carbonate powder, preferably from magnesite, dolomite, or hydromagnesite, is described. These oxide particles are characterized by high surface area, high porosity and a high degree of calcination, and the method of manufacture of utilizes an indirectly heated counterflow reactor. The oxides may be used as a powder, granules, or formulated into a slurry and used as a spray, emulsion, foam or fog, or the powder product may be directly applied. Also described is the formation of particles with microstructures defined by at least one nano-crystalline structure positioned on the outer surface of the particles.

A process and apparatus for manufacture of oxide products for use as biocide, chemical detoxifying, and catalytic support products, from caustic calcined carbonate powder, preferably from magnesite, dolomite, or hydromagnesite, is described. These oxide particles are characterized by high surface area, high porosity and a high degree of calcination, and the method of manufacture of utilizes an indirectly heated counterflow reactor. The oxides may be used as a powder, granules, or formulated into a slurry and used as a spray, emulsion, foam or fog, or the powder product may be directly applied. Also described is the formation of particles with microstructures defined by at least one nano-crystalline structure positioned on the outer surface of the particles.

A treatment method for a magnesium slag, comprises: Step a, producing magnesium particles and a crude solution of magnesium slag by digesting and sifting a magnesium slag; Step b, filtering the crude solution of magnesium slag sifted in Step a, so that mixed chlorides are obtained after a moisture in a filtrate is removed; Step c, obtaining a high purity magnesium oxide by dissolving a filter residue obtained in Step b via an ammonium sulfate method and a magnesium precipitation reaction as well as post-treatment. With the method, utilization of magnesium slag can reach up to more than 90% with a higher recycling rate, while the discharge of solid wastes can be reduced greatly which solid wastes are less contaminative to the environment, so that the contamination to the environment is greatly reduced and the required energy saving and emission reduction are also achieved.

Digestion of a laterite ore with sulfuric acid dissolves all constituents except silica. The resulting sulfatesaluminum sulfate, ferric sulfate, titanyl sulfate, and magnesium sulfateremain 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.

Digestion of a laterite ore with sulfuric acid dissolves all constituents except silica. The resulting sulfatesaluminum sulfate, ferric sulfate, titanyl sulfate, and magnesium sulfateremain 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.