A carbon dioxide recovery system that recovers carbon dioxide from a hybrid vehicle traveling in a CO.sub.2 recovery area including a CO.sub.2 recovery road in which a stationary CO.sub.2 recovery device collecting and recovering carbon dioxide from the atmosphere is provided acquires a residual charging capacity of the battery and position information of the hybrid vehicle and guides the hybrid vehicle such that the hybrid vehicle travels on the CO.sub.2 recovery road using a notification device when the residual charging capacity is equal to or less than a predetermined SOC threshold value while the hybrid vehicle is traveling in the CO.sub.2 recovery area.

A carbon dioxide (CO.sub.2) capture and utilization system captures CO.sub.2 from flue gas and utilizes the same to enhance algae or cyanobacteria growth. The system generally comprises a CO.sub.2 capture unit and a utilization unit that is in fluid communication with the CO.sub.2 capture unit. The CO.sub.2 capture unit includes a membrane CO.sub.2 absorber that captures CO.sub.2 from incoming flue gas to produce a CO.sub.2-rich solvent. The utilization unit processes the CO.sub.2-rich solvent to produce a product stream that includes CO.sub.2 and NH.sub.3 in a predetermined CO.sub.2:NH.sub.3 ratio. The product stream is delivered to a cultivation subsystem of the utilization of the unit including one or more species of algae or cyanobacteria. A method for capturing and utilizing CO.sub.2 is also provided herein.

A solvent system for the removal of acid gases from mixed gas streams is provided. Also provided is a process for removing acid gases from mixed gas streams using the disclosed solvent systems. The solvent systems may be utilized within a gas processing system.

Capture of hydrogen sulfide from a gas mixture may be accomplished using an aqueous solution comprising an amine. Certain sterically hindered amines may selectively form a reaction product with hydrogen sulfide under kinetically controlled contacting conditions and afford a light phase and a heavy phase above a critical solution temperature, wherein the hydrogen sulfide may be present in either phase. Upon separation of the light phase from the heavy phase, processing of one of the phases may take place to remove hydrogen sulfide therefrom. Recycling of the amine to an absorber tower may then take place to promote capture of additional hydrogen sulfide.

A power generation facility includes a process for capturing and sequestering CO2 generated from the facility turbines. The systems may include a heat recovery steam generator, a heat exchanger, a capture unit, and a sequestration compression unit that are configured to cool the flue gas, absorb CO2 therefrom, compress the flue gas, and send the compressed CO2 rich gas stream to sequestration of some form, thereby reducing the overall emissions from the facility.

In one embodiment, a carbon dioxide capturing system includes an absorber to absorb CO2 from first gas into lean liquid, and produce rich liquid that is the lean liquid absorbing the CO2 and second gas that is the first gas removing the CO2, and a regenerator to separate third gas including the CO2 from the rich liquid flowing from the absorber, and provide the lean liquid and the third gas. The system further includes a flowmeter to measure a flow rate of the third gas, a liquid level gauge to measure a liquid level of the lean liquid and/or the rich liquid, and a controller to regulate a quantity of heat energy supplied to the regenerator based on the flow rate of the third gas, and regulate a total amount of the lean liquid and the rich liquid in the system based on the liquid level.

A method of sequestering gaseous carbon dioxide in which an oxide is carbonated by contacting it with a first aqueous carbonate solution to convert a portion of the oxide into a carbonate, which precipitates from solution. By converting the oxide to a solid carbonate, the CO.sub.2 from the first carbonate solution is sequestered into the precipitate. At the same time, an aqueous hydroxide solution is formed. The aqueous hydroxide solution is contacted with gaseous carbon dioxide which sequesters the gaseous CO.sub.2 into a second aqueous carbonate solution. The second solution so generated is then recycled back into the process and used to convert the oxide into the precipitated carbonate.

A method and a plant for capturing CO2 from an incoming flue gas. The flue gas can be exhaust gas from coal and gas fired power plants, cement factories or refineries. The incoming exhaust gas is cooled, mixed with air and compressed, and thereafter introduced into a combustion chamber together with gas and/or liquid fuel. Part of the combustion is achieved by separate burners with cooling/combustion air feed with a volume equal to the volume of CO2 captured. Said burners will elevate the temperature in the combustion chamber allowing combustion of exhaust gas with low oxygen content. CO2 is captured at high partial pressure before expansion by the gas turbine to produce power and generate steam in the heat recovery unit. The gas turbine will operate with high efficiency close to design parameters with respect to inlet temperature, pressure and flow.

A carbon processing system comprises an air mover and a multi-stage reactor. The multi-stage reactor processes ambient air and generates carbon dioxide and generates exhausted gas released to ambient air. In operation, air contacts the base solution via the air mover. The air reacts with the base solution thereby generating a base solution having carbon dioxide and generating exhaust (absorption reaction). Next, the exhaust is released from the reactor. Next, heat is applied to the base solution having carbon dioxide thereby generating carbon dioxide and generating a base solution without carbon dioxide (desorption reaction). The base solution without carbon dioxide generated after applying heat is reusable in processing new air. The absorption reaction and desorption reaction are reversible reactions resulting in regeneration of the base solution into its form prior to contact with the air yielding high scalability and less processing volume as required by many conventional carbon processing techniques.

An emitter apparatus is mounted on a marine structure powered by wind or marine hydrokinetic energy to disperse a carbon dioxide sorbent such as sodium hydroxide. The sorbent can be generated by reverse osmosis of seawater with electrolysis of the brine, or delivered from an external supply. Suitable marine structures include offshore wind turbines, marine hydrokinetic generators, offshore oil platforms, merchant vessels, and other fixed and mobile structures. Effective capture is made by dispersing a fine mist or fog of aqueous sorbent from nozzles with a particle size from a nozzle of less than 100 microns. The sorbent reacts with atmospheric carbon dioxide forming carbonates and bicarbonates, which drift and fall to the ocean surface, reducing surface acidity and capturing additional atmospheric carbon dioxide via absorption at the local ocean surface. The resulting carbonates sink to the ocean floor and are there sequestered.