A process for treating a sulfurous fluid to form gypsum and magnesium carbonate, whereby the sulfurous fluid is scrubbed with a sequestrating agent to yield a scrubbed fluid, gypsum and magnesium sulfate. The flue gas desulfurized gypsum is isolated from the magnesium sulfate solution by filtration or centrifugation. The magnesium sulfate is reacted with a carbonate salt to produce a magnesium carbonate whereby the reaction conditions are controlled to control the properties of the magnesium carbonate produced.

Described herein is a dry sorbent injection system and process for removing sulfur oxides from a flue gas. The process generally comprises treating the flue gas with a dry sorbent material to convert the sulfur oxides to sodium sulfate particulates. The sodium sulfate particulates may then be introduced into a mix tank with water to form sodium sulfate solution. The sodium sulfate solution may then be reacted with a calcium hydroxide slurry to produce a reaction mixture comprising calcium sulfate precipitate and a sodium hydroxide solution. The calcium sulfate (gypsum) may be recovered, and the sodium hydroxide solution may be recirculated to pre-treat the flue gas by removing at least a portion of the sulfur dioxide and/or cooling the flue gas stream.

A process for converting natural calcium carbonate into precipitated calcium carbonate, involving treating the natural calcium carbonate with a sulfate to produce a gypsum and reacting the gypsum with at least one carbonate source to produce precipitated calcium carbonate. The crystalline polymorph, particle size, and various other characteristics of the precipitated calcium carbonate are controlled by varying conditions during the reacting. Since the natural calcium carbonate is not calcined, the process relates to a low energy method of producing precipitated calcium carbonate of controlled polymorph and particle size with limestone, marble, or chalk as the calcium source.

A method for production of ammonium phosphate from phosphate rock slurry. The method includes: introducing flue gas containing SO.sub.2 into a phosphate rock slurry, to yield an absorption solution; evaporating waste ammonia water containing 10-20 wt. % ammonia to yield ammonia gas; introducing the ammonia gas into the absorption solution at a temperature of 110-135° C. until a neutralization degree of the absorption solution reaches 1.5-1.6, thus yielding an ammonium phosphate solution and calcium sulfate; separating the calcium sulfate from the ammonium phosphate solution; and introducing the ammonium phosphate solution to a granulator for granulation to yield ammonium phosphate granules; drying and sieving the ammonium phosphate granules, thereby yielding ammonium phosphate.

A process and system are disclosed for producing lithium oxide from lithium nitrate. In the process and system, the lithium nitrate is thermally decomposed in a manner such that a fraction of the lithium nitrate forms lithium oxide, and such that a remaining fraction of the lithium nitrate does not decompose to lithium oxide. The thermal decomposition may be terminated after a determined time period to ensure that there is a remaining fraction of lithium nitrate and to thereby produce a lithium oxide in lithium nitrate product. The lithium oxide in lithium nitrate product may have one or more transition-metal oxides, hydroxides, carbonates or nitrates added thereto to form a battery electrode. The lithium oxide in lithium nitrate product may alternatively be subjected to carbothermal reduction to produce lithium metal.

The present disclosure provides systems for carbon capture in combination with production of one or more industrially useful materials. The disclosure also provides methods for carrying out carbon capture in combination with an industrial process. In particular, carbon capture can include carrying out calcination in a reactor, separation of carbon dioxide rich flue gases from industrially useful products, and capture of at least a portion of the carbon dioxide for sequestration of other use, such as enhanced oil recovery.

A method for sequestering CO.sub.2 by creating precipitated calcium carbonates including Calcite, Dolomite, Vaterite and Struvite; (1) Utilizing a mutually beneficial bacterial/algal colony that can fix CO.sub.2 as Calcite, Dolomite, Vaterite and Struvite (2) providing sunlight, water, CO.sub.2 from either the air or industrial waste streams; and (3) assisting microbial/algal induced carbonate precipitation of Calcite, Dolomite, Vaterite and Struvite, thereby sequestering most of the CO.sub.2 introduced in step (2). In addition, chlorine, sulfur, H.sub.2S, NOx and toxic heavy metals will be fixed into the Calcite, Dolomite, Vaterite and/or Struvite matrix, rendering them environmentally harmless.

The present disclosure provides systems for carbon capture in combination with production of one or more industrially useful materials. The disclosure also provides methods for carrying out carbon capture in combination with an industrial process. In particular, carbon capture can include carrying out calcination in a reactor, separation of carbon dioxide rich flue gases from industrially useful products, and capture of at least a portion of the carbon dioxide for sequestration of other use, such as enhanced oil recovery.

A device includes a desulfurization system which forms a hydrogen sulfide-containing acid gas; a system for extracting elemental sulfur and a hydrogen sulfide-containing tail gas as exhaust gas; a device for generating electricity and gypsum from the tail gas; and a gas line system for supplying acid gas from the desulfurization system to the system for extracting elemental sulfur and to the device for generating electricity and gypsum, and for supplying tail gas from the system for extracting elemental sulfur to the device for generating electricity and gypsum. The gas line system has a gas distributing apparatus which supplies acid gas solely to the system in a first position, supplies acid gas solely to the device in a second position, and supplies a first part of the acid gas to the system and a second part of the acid gas to the device in a distributing position.

A method of managing sulfur in a sulfur-containing stream may include steps of providing a sulfur-containing stream; converting sulfur within the sulfur-containing stream to elemental sulfur; transporting the elemental sulfur to a location at or near a sulfur oxide injection location; converting the elemental sulfur to sulfur oxides; recovering electrical energy from said step of converting the elemental sulfur to sulfur oxides; injecting the sulfur oxides into the sulfur oxide injection location. The method may include steps of screening a plurality of injection locations and selecting, from the screened plurality of injection locations, a particular sulfur dioxide injection location with specific reservoir characteristics for the sulfur oxides.