Systems and methods for preventing formation of carbonyl sulfide in the production of sweet gas using an amine-lean aqueous solution and metal oxide adsorbent material. In embodiments, a method may include producing, via an amine absorption column supplied with a raw gas stream that includes fractions of hydrogen sulfide (H.sub.2S), carbon dioxide (CO.sub.2), and carbon monoxide (CO), (1) a sweet gas stream that includes the fractions of the CO and (2) an amine-rich aqueous solution that includes the H.sub.2S and CO.sub.2. The method may include heating the amine-rich aqueous solution to produce a heated amine-rich aqueous solution. The method may include producing, via an amine regenerator supplied with the heated amine-rich aqueous solution (1) an acid gas stream that includes the H.sub.2S and CO.sub.2 and (2) an amine-lean aqueous solution. The method may include producing, via adsorption in a metal oxide adsorbent vessel, an effluent stream that includes the CO.sub.2.

A process for selectively separating H.sub.2S from a gas mixture which also comprises CO.sub.2 is disclosed. A stream of the gas mixture is contacted with an absorbent solution comprising one or more amines, alkanolamines, hindered alkanolamines, capped alkanolamines, or mixtures thereof. The H.sub.2S/CO.sub.2 selectivity of the absorbent solution is preferably greater than about 4.0 for an acid gas loading [mol(CO.sub.2+H.sub.2S)/mol(amine)] between about 0.2 and about 0.6, and is achieved by reducing pH of the absorbent solution.

The absorption agent of the present invention contains water, an amine compound, and an organic solvent, and a value obtained by subtracting a solubility parameter of the organic solvent from a solubility parameter of the amine compound is 1.1 (cal/cm.sup.3).sup.1/2 or more and 4.2 (cal/cm.sup.3).sup.1/2 or less. The method for separation and recovery of an acidic compound of the present invention includes the steps of: bringing a mixed gas containing an acidic compound into contact with an absorption agent containing water, an amine compound, and an organic solvent to absorb the acidic compound into the absorption agent; causing the absorption agent that has absorbed the acidic compound to be phase-separated into a first phase containing the acidic compound in a high content and a second phase containing the acidic compound in a low content; and heating the first phase to release the acidic compound from the first phase.

A scrubbing solution for removing contaminants, including particularly hydrogen sulfide, from a fluid. The scrubbing solution includes at least one scrubbing reagent which has a primary or secondary amine and an acid, which may be phosphoric acid. The fluid being scrubbed is passed through the scrubbing solution. The contaminants react with the scrubbing reagent securing them in the scrubbing solution. The fluid being scrubbed and the scrubbing solution are then separated. The scrubbing solution is heated and, if the scrubbing solution is under pressure, the pressure is reduced. The acid facilitates thorough removal of the contaminants, and especially the hydrogen sulfide, from the scrubbing solution. The scrubbing solution is then ready for reuse. Because the scrubbing solution is rendered substantially free of hydrogen sulfides, it can absorb other sulfide contaminants that might not otherwise be absorbed.

Embodiments of a composition of the present invention for scavenging sulfides from hydrocarbon fluids and water generally include diaminol/diaminacetal provided in a chemical system, wherein the diaminol/diaminacetal is prepared by reacting one molar equivalent of glyoxal and two molar equivalents of a primary amine functionality. In various embodiments, the chemical system includes at least one component selected from surfactants, hydrotropes, alcohols, amines, amino acids, and ethers. Embodiments of a method for scavenging sulfides from hydrocarbon fluids and water is also provided.

In a process for removal of acid gases from a fluid stream the fluid stream is contacted with an absorbent to obtain a treated fluid stream and a laden absorbent. The absorbent comprises a diluent and a compound of the general formula (I) wherein R.sup.1 is C.sub.1-C.sub.3-alkyl; R.sup.2 is C.sub.1-C.sub.3-alkyl; R.sup.3 is selected from hydrogen and C.sub.1-C.sub.3-alkyl; and R.sup.4 is selected from hydrogen and C.sub.1-C.sub.3-alkyl. ##STR00001##

Disclosed is a process for regenerating a hybrid solvent used to remove contaminants from a fluid stream and to provide an improved yield of purified fluid. Said process comprises a purification unit (12) and at least one regeneration unit (40) wherein make-up water (72) is added to the regenerated lean hybrid solvent (55) prior to reuse in the first purification unit and no water is recycled into the regeneration unit.

Methods and systems are provided for a multiplexed phase separating inertial filter that is composed of helical through holes generating centrifugal separating forces. In one example, the inertial filter may be a planar porous material with an array of helical channels, each helical channel of the array of helical channels extending from a top surface of the porous material to a bottom surface of the porous material.

A method for maintaining solvent quality in a gas treating system involves calculating, by an advisory system for continuous monitoring of the gas treating system, a water content deficit in the solvent of the gas treating system, calculating, by the advisory system, a water makeup rate compensating for the water content deficit, and displaying, in an interactive user interface of the advisory system, the water makeup rate.

A system and a process for capturing Carbon Dioxide (CO.sub.2) from flue gases are disclosed. The process comprises feeding a flue gas comprising CO.sub.2 to at least one Rotary Packed Bed (RPB) absorber rotating circularly. A solvent may be provided through an inner radius of the RPB absorber. The solvent may move towards an outer radius of the RPB absorber. The solvent may react with the flue gas in a counter-current flow. The process further includes passing the flue gas through at least one of a water wash and an acid wash to remove traces of the solvent present in the flue gas. Finally, the solvent reacted with the CO.sub.2 may be thermally regenerated for re-utilizing the solvent back in the process.