A method for preparing a cathode active material precursor for a secondary battery, including: moving a co-precipitation filtrate generated after a co-precipitation reaction to a co-precipitation filtrate storage tank; removing a metal hydroxide by passing the co-precipitation filtrate through a filter; reacting the co-precipitation filtrate from which the metal hydroxide is removed with sulfuric acid or nitric acid to produce an ammonium sulfate or an ammonium nitrate while removing ammonia from the co-precipitation filtrate from which the metal hydroxide is removed; cooling and crystallizing the co-precipitation filtrate from which the metal hydroxide and ammonia are removed to precipitate a sodium sulfate; filtering the precipitated sodium sulfate to separate the precipitated sodium sulfate from the co-precipitation filtrate from which the metal hydroxide and ammonia are removed; drying the sodium sulfate separated from the co-precipitation filtrate and moving the co-precipitation filtrate separated from the sodium sulfate to a circulation concentration tank; and heating the co-precipitation filtrate stored in the circulation concentration tank to a predetermined temperature for recycling and performing N.sub.2 purging or bubbling, is provided.

A method for preparing a cathode active material precursor for a secondary battery, including: moving a co-precipitation filtrate generated after a co-precipitation reaction to a co-precipitation filtrate storage tank; removing a metal hydroxide by passing the co-precipitation filtrate through a filter; reacting the co-precipitation filtrate from which the metal hydroxide is removed with sulfuric acid or nitric acid to produce an ammonium sulfate or an ammonium nitrate while removing ammonia from the co-precipitation filtrate from which the metal hydroxide is removed; cooling and crystallizing the co-precipitation filtrate from which the metal hydroxide and ammonia are removed to precipitate a sodium sulfate; filtering the precipitated sodium sulfate to separate the precipitated sodium sulfate from the co-precipitation filtrate from which the metal hydroxide and ammonia are removed; drying the sodium sulfate separated from the co-precipitation filtrate and moving the co-precipitation filtrate separated from the sodium sulfate to a circulation concentration tank; and heating the co-precipitation filtrate stored in the circulation concentration tank to a predetermined temperature for recycling and performing N.sub.2 purging or bubbling, is provided.

Processes and systems for producing potassium sulfate as a byproduct of a desulfurization process. Sulfur dioxide is absorbed from a flue gas using an ammonia-containing solution to produce an ammonium sulfate solution that contains dissolved ammonium sulfate. At least a first portion of the ammonium sulfate solution is heated before dissolving potassium chloride therein to form a slurry that contains potassium sulfate crystals and an ammonium chloride solution. The slurry is then cooled to precipitate additional potassium sulfate crystals, after which the potassium sulfate crystals are removed to yield a residual ammonium chloride solution that contains dissolved ammonium chloride and residual dissolved potassium sulfate. Ammonia is then absorbed into the residual ammonium chloride solution to further precipitate potassium sulfate crystals, which are removed to yield a residual ammonium chloride solution that is substantially free of dissolved potassium sulfate.

Processes and systems for producing potassium sulfate as a byproduct of a desulfurization process. Sulfur dioxide is absorbed from a flue gas using an ammonia-containing solution to produce an ammonium sulfate solution that contains dissolved ammonium sulfate. At least a first portion of the ammonium sulfate solution is heated before dissolving potassium chloride therein to form a slurry that contains potassium sulfate crystals and an ammonium chloride solution. The slurry is then cooled to precipitate additional potassium sulfate crystals, after which the potassium sulfate crystals are removed to yield a residual ammonium chloride solution that contains dissolved ammonium chloride and residual dissolved potassium sulfate. Ammonia is then absorbed into the residual ammonium chloride solution to further precipitate potassium sulfate crystals, which are removed to yield a residual ammonium chloride solution that is substantially free of dissolved potassium sulfate.

A method of producing potassium sulfate by employing sodium sulfate and potassium chloride sources is disclosed. The method includes a crystallization process that yields a mother liquor containing sulfate, sodium and chloride. The mother liquor is directed to an anion segregation unit that produces a reject or retentate rich in sulfate which is recycled and employed in the production of the potassium sulfate. Further, the anion segregation unit produces a permeate that is depleted in sulfate but includes sodium and chloride and is directed to a sodium chloride crystallizer for producing sodium chloride.

A method of producing potassium sulfate by employing sodium sulfate and potassium chloride sources is disclosed. The method includes a crystallization process that yields a mother liquor containing sulfate, sodium and chloride. The mother liquor is directed to an anion segregation unit that produces a reject or retentate rich in sulfate which is recycled and employed in the production of the potassium sulfate. Further, the anion segregation unit produces a permeate that is depleted in sulfate but includes sodium and chloride and is directed to a sodium chloride crystallizer for producing sodium chloride.

A method of producing potassium sulfate by employing sodium sulfate and potassium chloride sources is disclosed. The method includes a crystallization process that yields a mother liquor containing sulfate, sodium and chloride. The mother liquor is directed to an anion segregation unit that produces a reject or retentate rich in sulfate which is recycled and employed in the production of the potassium sulfate. Further, the anion segregation unit produces a permeate that is depleted in sulfate but includes sodium and chloride and is directed to a sodium chloride crystallizer for producing sodium chloride.

A method of producing potassium sulfate by employing sodium sulfate and potassium chloride sources is disclosed. The method includes a crystallization process that yields a mother liquor containing sulfate, sodium and chloride. The mother liquor is directed to an anion segregation unit that produces a reject or retentate rich in sulfate which is recycled and employed in the production of the potassium sulfate. Further, the anion segregation unit produces a permeate that is depleted in sulfate but includes sodium and chloride and is directed to a sodium chloride crystallizer for producing sodium chloride.

The present invention relates to a method for producing a potassium sulfate containing fertilizer composition from a sodium sulfate containing residue process stream of a battery manufacturing facility, battery recycling facility, or steel production plant, wherein residue process stream from a battery manufacturing facility, battery recycling facility, or steel production plant is provided; optionally water is provided; potassium chloride is provided; and a reaction mixture is provided comprising said optional water, potassium chloride and residue process stream, and is allowed to react, wherein potassium sulfate is obtained.

Processes and systems for producing potassium sulfate as a byproduct of a desulfurization process. Sulfur dioxide is absorbed from a flue gas using an ammonia-containing solution to produce an ammonium sulfate solution that contains dissolved ammonium sulfate. At least a first portion of the ammonium sulfate solution is heated before dissolving potassium chloride therein to form a slurry that contains potassium sulfate crystals and an ammonium chloride solution. The slurry is then cooled to precipitate additional potassium sulfate crystals, after which the potassium sulfate crystals are removed to yield a residual ammonium chloride solution that contains dissolved ammonium chloride and residual dissolved potassium sulfate. Ammonia is then absorbed into the residual ammonium chloride solution to further precipitate potassium sulfate crystals, which are removed to yield a residual ammonium chloride solution that is substantially free of dissolved potassium sulfate.