An aminal compound is injected into a fluid gas stream including at least one acid gas to reduce the amount of acid gas in the fluid gas stream. Having two reactive sites present in the aminal compound enables a much higher efficiency of acid gas capture than a simple alkanolamine, which isn't effective, for example, under dilute circumstances.

A reclaimer system and methods for using said reclaimer system to reclaim one or more amine agents from a fluid containing one or more degradation products that have been formed from the reaction of one or more acid gas components with the one or more amine agents.

A method and systems are provided for controlling degradation in a reboiler using a hydrophobic coating. A reboiler is provided that includes a steam shell and a plurality of tubes. The reboiler includes a low surface-energy coating on a surface of the plurality of tubes.

An oxidation resistant absorbent for capturing carbon dioxide from a gas stream. The oxidation resistant absorbent includes an alkanolamine with a weight percent in a range of 10 wt. % to 35 wt. % to a total amount of the oxidation resistant absorbent, a base with a weight percent in a range of 1 wt. % to 15 wt. % to a total amount of the oxidation resistant absorbent, a plurality of nanoparticles with a weight percent in a range of 0.1 wt. % to 3 wt. % to a total amount of the oxidation resistant absorbent, and water.

The present disclosure relates to a porous liquid or a porous liquid enzyme system that includes a high surface area solid and a liquid film substantially covering the high surface area solid. The porous liquid or porous liquid enzyme may be contacted with a fluid that is immiscible with the liquid film such that a liquid-fluid interface is formed. The liquid film may facilitate mass transfer of a substance or substrate across the liquid-fluid interface. The present disclosure also provides methods of performing liquid-based extractions and enzymatic reactions utilizing the porous liquid or porous liquid enzyme of the present disclosure. The present disclosure also provides methods for selecting the components of the porous liquid or a porous liquid enzyme system and methods of self-replenishing the used liquid coating.

The invention relates to a method for removing absorbable gases from pressurized industrial gases contaminated with absorbable gases, without supplying cooling energy. The method includes an industrial gas that is to be purified is purified by an absorbent solvent, the absorbable gases situated therein being removed by the solvent, and the loaded solvent is passed to a stripping stage in which the absorbed gas is desorbed again, and the desorbed gas is compressed, in such a manner that it is heated by the compression, whereupon it is cooled to standard temperature by means of cooling water or cooling air, then expanded, in such a manner that it cools and this cooled desorption gas is again returned to the industrial gas, in such a manner that said industrial gas is also cooled by the admixture.

A CO.sub.2 recovery unit includes a CO.sub.2 absorber that brings a gas having a low CO.sub.2 concentration into countercurrent contact with a CO.sub.2 absorbent to remove CO.sub.2 from the gas. The CO.sub.2 recovery unit further includes a first absorbent circulation line that supplies a CO.sub.2 absorbent from a first CO.sub.2 absorption section as a first circulation solution to an upper side of a first CO.sub.2 absorption section; a second absorbent circulation line that supplies a CO.sub.2 absorbent from a second CO.sub.2 absorption section as a second circulation solution to an upper side of a second CO.sub.2 absorption section; and an absorbent discharge line that discharges a part of the first circulation solution from the first absorbent circulation line and supply the part of the first circulation solution as a discharged solution to the second absorbent circulation section.

A system and process for selectively separating H.sub.2S from a gas mixture which also comprises CO.sub.2 is disclosed. A water recycle stream is fed to the absorber in order to create a higher concentration absorbent above the recycle feed and having a greater H.sub.2S selectivity at lower acid gas loadings, and a more dilute absorbent below the recycle feed and having a greater H.sub.2S selectivity at higher acid gas loadings. Also disclosed is a system and process for selectively separating H.sub.2S by utilizing two different absorbents, one absorbent for the upper section of the absorber, tailored to have a greater H.sub.2S selectivity at lower acid gas loadings, and a second absorbent for the lower section of the absorber, tailored to have a greater H.sub.2S selectivity at higher acid gas loadings.

Compositions with supramolecular structures for use in oil and gas production and other applications include an H.sub.2S scavenger, a supramolecular host chemical or a supramolecular guest chemical configured to engage in host-guest chemistry with the scavenger, and a solvent. Methods of controlling H.sub.2S at a production site include applying an effective amount of the composition to the production stream.

The invention generally relates to processes for reducing fouling in amine systems and to equipment useful in such processes. Such amine systems are useful for removing one or more acidic gases such as CO.sub.2 or H.sub.2S from olefin containing hydrocarbon streams. The invention generally relates to minimizing residence time of foulant and foulant precursors at the relatively high temperature found in the amine regenerator and/or to purging the foulant and foulant precursors from the regenerator system. This is accomplished by operating the regenerator column as a stripper (no reflux) and re-routing reflux liquid containing foulant or foulant precursors to a processing location that is less prone to fouling or, optionally, by replacing the reflux liquid with fresh make-up amine or water.