The invention relates to a process for preparing alkali carbonate/bicarbonate salts, comprising continuously feeding aqueous alkali hydroxide solution into a gas-liquid contactor; forcing incoming CO.sub.2-containing gas stream through a sparging device submerged in the gas-liquid contactor below the surface level of the aqueous alkali hydroxide solution, to generate bubbles and/or microbubbles; adding hydrogen peroxide in proximity to orifices of the sparging device, from which the bubbles and/or microbubbles evolve, wherein the supply of hydrogen peroxide is adjusted to decrease alkali carbonate formation and increase alkali bicarbonate formation; and continuously discharging an effluent from the gas-liquid contactor and recovering therefrom carbonate and bicarbonate alkali salts predominated by the bicarbonate component. A gas liquid-contactor and an apparatus are also provided by the invention.

A process for the recovery of lithium carbonate from a solution (1) containing a mixture of lithium sulfate and lithium hydroxide, the process comprising the precipitation of lithium carbonate (3) from the solution (1) containing a mixture of lithium sulfate and lithium hydroxide through the addition of carbon dioxide (2).

A process for the recovery of lithium carbonate from a solution (1) containing a mixture of lithium sulfate and lithium hydroxide, the process comprising the precipitation of lithium carbonate (3) from the solution (1) containing a mixture of lithium sulfate and lithium hydroxide through the addition of carbon dioxide (2).

The disclosure provides seven integrated methods for the chemical sequestration of carbon dioxide (CO.sub.2), nitric oxide (NO), nitrogen dioxide (NO.sub.2) (collectively NOR, where x=1, 2) and sulfur dioxide (SO.sub.2) using closed loop technology. The methods recycle process reagents and mass balance consumable reagents that can be made using electrochemical separation of sodium chloride (NaCl) or potassium chloride (KCl). The technology applies to marine and terrestrial exhaust gas sources for CO.sub.2, NOx and SO.sub.2. The integrated technology combines compatible and green processes that capture and/or convert CO.sub.2, NOx and SO.sub.2 into compounds that enhance the environment, many with commercial value.

The disclosure provides seven integrated methods for the chemical sequestration of carbon dioxide (CO.sub.2), nitric oxide (NO), nitrogen dioxide (NO.sub.2) (collectively NOR, where x=1, 2) and sulfur dioxide (SO.sub.2) using closed loop technology. The methods recycle process reagents and mass balance consumable reagents that can be made using electrochemical separation of sodium chloride (NaCl) or potassium chloride (KCl). The technology applies to marine and terrestrial exhaust gas sources for CO.sub.2, NOx and SO.sub.2. The integrated technology combines compatible and green processes that capture and/or convert CO.sub.2, NOx and SO.sub.2 into compounds that enhance the environment, many with commercial value.

The present invention provides a method for treating a gas, comprising: step (A): collecting a gas comprising carbon dioxide and fine particulate matter; step (B): rinsing the gas with water to obtain a rinsed gas; and step (C): contacting the rinsed gas with a basic solution in a way of co-current flow to absorb the carbon dioxide in the rinsed gas by the basic solution to obtain a treated gas and a weak basic solution; wherein the pH value of the basic solution is between 9 and 14, and the pH value of the weak basic solution is between 8 and 8.5. The method can reduce the content of both fine particulate matter and carbon dioxide.

The disclosure provides seven integrated methods for the chemical sequestration of carbon dioxide (CO.sub.2), nitric oxide (NO), nitrogen dioxide (NO.sub.2) (collectively NO.sub.x, where x=1, 2) and sulfur dioxide (SO.sub.2) using closed loop technology. The methods recycle process reagents and mass balance consumable reagents that can be made using electrochemical separation of sodium chloride (NaCl) or potassium chloride (KCl). The technology applies to marine and terrestrial exhaust gas sources for CO.sub.2, NOx and SO.sub.2. The integrated technology combines compatible and green processes that capture and/or convert CO.sub.2, NOx and SO.sub.2 into compounds that enhance the environment, many with commercial value.

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 system and method for heat produced at a nuclear power plant as the energy source for carbon dioxide sequestration while simultaneously producing electricity. The system includes a nuclear power plant that differs significantly from conventional designs inasmuch as its design is tightly integrated into the carbon dioxide sequestration system. The system generates electricity and sequesters carbon dioxide at the same time. Instead of simply generating electricity from the nuclear reactor and then using that electricity to run a sequestration process, the method is designed to directly provide the requisite thermal energy to the sequestration process, and simultaneously power an electrical generator. Another feature of the system design is a method of optimizing load balancing between the electrical grid and carbon dioxide sequestration.

There are provided processes comprising submitting an aqueous composition comprising lithium sulphate and/or bisulfate to an electrolysis or an electrodialysis for converting at least a portion of said sulphate into lithium hydroxide. During electrolysis or electrodialysis, the aqueous composition is at least substantially maintained at a pH having a value of about 1 to about 4; and converting said lithium hydroxide into lithium carbonate. Alternatively, lithium sulfate and/or lithium bisulfate can be submitted to a first electromembrane process that comprises a two-compartment membrane process for conversion of lithium sulfate and/or lithium bisulfate to lithium hydroxide, and obtaining a first lithium-reduced aqueous stream and a first lithium hydroxide-enriched aqueous stream; and submitting said first lithium-reduced aqueous stream to a second electromembrane process comprising a three-compartment membrane process to prepare at least a further portion of lithium hydroxide and obtaining a second lithium-reduced aqueous stream and a second lithium-hydroxide enriched aqueous stream.