A gas pressurized separation system strips a product gas from a stream yielding a high pressure gaseous effluent containing the product gas such as may be used to capture CO.sub.2 from coal fired post combustion flue gas capture and to purify natural gas, syngas and EOR recycle gas. The system comprises a gas pressurized stripping column allowing flow of one or more raw streams in a first direction and allowing flow of one or more high pressure gas streams in a second direction, to strip the product gas into the high pressure gas stream and yield a high pressure gaseous effluent that contains the product gas. The process can further comprise a final separation process to further purify the product gas from the GPS column. For CO.sub.2 product, a preferred energy efficient final separation process, compound compression and refrigeration process, is also introduced.

A carbon dioxide capture process system includes an absorber vessel, a stripper, a first group of sensors and a second group[ of sensors. The first group of sensors is adapted for collecting real-time temperature, pH, density and viscosity data for a lean carbon capture solvent used for carbon capture from an acid gas adjacent the lean carbon capture solvent inlet. The second group of sensors is adapted for collecting real-time temperature, pH, density and viscosity data for a rich carbon capture solvent following carbon capture from the acid gas adjacent the rich carbon capture solvent inlet. A control system and related method are also described.

The present invention relates to a method for using, as a carbon dioxide absorbent, a secondary amine having a nitrile group, that is, a 3-(alkylamino)propionitrile compound. The absorbent based on the 3-(alkylamino)propionitrile compound and the carbon dioxide absorption method and separation method using same, according to the present invention, not only have an excellent carbon dioxide absorption capacity and a rapid carbon dioxide absorption rate, but also allow absorbent regeneration even at a considerably low temperature compared with a conventional alkanolamine-based absorbent and thus can significantly reduce the entire energy consumption required for an absorption process, and can also prevent recovered carbon dioxide from being contaminated with moisture and absorbent vapor, owing to the low regeneration temperature.

A CO.sub.2 recovery device is provided with a CO.sub.2 absorption tower and an absorption-solution regeneration tower. The CO.sub.2 absorption tower includes: a CO.sub.2 absorption section in which CO.sub.2-containing flue gas is brought into contact with a CO.sub.2 absorption solution, namely a basic-amine-compound absorption solution, so as to remove CO.sub.2 from the CO.sub.2-containing flue gas; and a water-washing section in which decarbonated flue gas from which CO.sub.2 has been removed is brought into contact with washing water so as to remove accompanying substances accompanying the decarbonated flue gas. The absorption-solution regeneration tower regenerates the CO.sub.2 absorption solution that has absorbed CO.sub.2. This CO.sub.2 recovery device, in which a lean solution from which CO.sub.2 has been removed is reused in the CO.sub.2 absorption tower, has an aldehyde-removing agent supply unit that supplies a sulfite-compound aldehyde removing agent to a circulating washing-water line that circulates the washing water to the water-washing section.

A degradant concentration measurement device 14 according to the invention has an electric conductivity measurement instrument 71A measuring the electric conductivity of a lean solution 16 that is an acidic gas-absorbing solution and detection means 72 obtaining the concentration of a degradant contained in a lean solution 16 from the measured electric conductivity of the lean solution 16 based on the relationship between the previously-obtained electric conductivity of the lean solution 16 and the concentration of the degradant contained in the lean solution 16.

The invention relates to methods and systems for determining operating and/or dimensioning parameters of a gas treatment plant including at least one gas treatment unit as well as methods and systems for generating a request to initiate the determination of operating and/or dimensioning parameters of a gas treatment plant. The invention further relates to a computer program and non-volatile or non-transitory storage medium with the computer program, which when executed on one or more processors, performs one or more of the methods.

A method of removing impurities from a natural gas stream. A selective solvent is provided that absorbs a first impurity at a first rate and a second impurity at a second rate that is slower than the first rate. The solvent is cooled to a temperature below 60° F. to provide a cooled solvent. The cooled solvent is contacted with the natural gas stream, thereby generating a rich solvent that includes the first impurity. The rich solvent is removed from the natural gas stream, wherein an amount of the first impurity remaining in the natural gas stream is below a sales gas requirement.

An organic amine decarbonization solution includes: i) one or more organic amines serving as a carbon dioxide absorbent; and ii) an antioxidant. The antioxidant includes: a) one or more organometallic complexes of Formula [M.sub.x(L).sub.y]A.sub.n, wherein each M independently represents a central atom selected from the group consisting of transition metals, Group IVA metals and Group VA metals at a lower valence state; each L independently represents a bidentate or multidentate organic ligand with each ligating atom thereof being independently one of O, S, N and P; each A independently represents an uncoordinated counter-ion suitable for forming an outer sphere of a complex; x is 1, 2 or 3; y is 1, 2, 3, 4, 5, 6, 7 or 8; and n is 0, 1, 2, 3 or 4; and b) optionally one or more metal chelating agents.

A system for absorbing and separating acid gases may include an absorbing tower in which a gas containing an acid gas is supplied, a recycling tower that is disposed close to the absorbing tower, an absorbent that absorbs an acid gas in the absorbing tower and discharges the acid gas back to the recycling tower while circulating through the absorbing tower and the recycling tower, and a condenser that is connected to the recycling tower and condenses an acid gas produced in the recycling tower, wherein a centrifugal separator that separates the absorbent, using a centrifugal force, is disposed at a lower portion in the absorbing tower.

An absorbent for selective removal of hydrogen sulfide over carbon dioxide from a fluid stream comprises an aqueous solution of a) a tertiary amine, b) a sterically hindered secondary amine of the general formula (I) ##STR00001##
in which R.sub.1 and R.sub.2 are each independently selected from C.sub.1-4-alkyl and C.sub.1-4-hydroxyalkyl; R.sub.3, R.sub.4, R.sub.5 and R.sub.6 are each independently selected from hydrogen, C.sub.1-4-alkyl and C.sub.1-4-hydroxyalkyl, with the proviso that at least one R.sub.4 and/or R.sub.5 radical on the carbon atom bonded directly to the nitrogen atom is C.sub.1-4-alkyl or C.sub.1-4-hydroxyalkyl when R.sub.3 is hydrogen; x and y are integers from 2 to 4 and z is an integer from 1 to 4; where the molar ratio of b) to a) is in the range from 0.05 to 1.0, and c) an acid in an amount, calculated as neutralization equivalent relative to the protonatable nitrogen atoms in a) and b), of 0.05 to 15.0%. One preferred amine of the formula I is 2-(2-tert-butylaminoethoxy)ethanol. The absorbent allows a defined H.sub.2S selectivity to be set at pressures of the kind typical in natural gas processing.