Abstract: 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.

Abstract: Proppant particulates like sand are commonly used in hydraulic fracturing operations to maintain one or more fractures in an opened state following the release of hydraulic pressure. Fracturing fluids and methods of hydraulic fracturing may also use proppant particulates composed of fluid coke material (also referred to as fluid coke proppant particulates). In some instances, the fluid coke proppant particulates are characterized by a bulk density of less than about 0.9 grams per cubic centimeter.

Abstract: Proppant particulates like sand are commonly used in hydraulic fracturing operations to maintain one or more fractures in an opened state following the release of hydraulic pressure. Fracturing fluids and methods of hydraulic fracturing may also use proppant particulates composed of flexicoke material. Such proppant particulates may have improved transport into fractures because of lower density than traditional proppants like sand and may produce fewer fines that reduce fluid flow through proppant packs.

Abstract: A process for selectively separating H2S from a gas mixture which also comprises CO2is 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 H2S/CO2 selectivity of the absorbent solution is preferably greater than about 4.0 for an acid gas loading [mol(CO2+H2S)/mol(amine)] between about 0.2 and about 0.6, and is achieved by reducing pH of the absorbent solution.

Abstract: An absorbent for the selective removal of hydrogen sulfide from a fluid stream comprising carbon dioxide and hydrogen sulfide, wherein the absorbent contains an aqueous solution, comprising: a) an amine or a mixture of amines of the general formula (I) wherein R1 is C1-C5-alkyl; R2 is C1-C5-alkyl; R3 is selected from hydrogen and C1-C5-alkyl; x is an integer from 2 to 10; and b) an ether or a mixture of ethers of the general formula (II): R4—[O—CH2—CH2]y—OH; wherein R4 is C1-C5-alkyl; and y is an integer from 2 to 10; wherein R1 and R4 are identical; wherein the mass ratio of b) to a) is from 0.08 to 0.5. The absorbent is suitable for the selective removal of hydrogen sulfide from a fluid stream comprising carbon dioxide and hydrogen sulfide. The absorbent has a reduced tendency for phase separation at temperatures falling within the usual range of regeneration temperatures for the aqueous amine mixtures and is easily obtainable.

Abstract: A process for selectively separating H2S from a gas mixture which also comprises CO2 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 H2S/CO2 selectivity of the absorbent solution is preferably greater than about 4.0 for an acid gas loading [mol(CO2+H2S)/mol(amine)] between about 0.2 and about 0.6, and is achieved by reducing pH of the absorbent solution.

Abstract: 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 R1 is C1-C3-alkyl; R2 is C1-C3-alkyl; R3 is selected from hydrogen and C1-C3-alkyl; and R4 is selected from hydrogen and C1-C3-alkyl.

Abstract: Proppant particulates like sand are commonly used in hydraulic fracturing operations to maintain one or more fractures in an opened state following the release of hydraulic pressure. Fracturing fluids and methods of hydraulic fracturing may also use proppant particulates composed of flexicoke material. Such proppant particulates may have improved transport into fractures because of lower density than traditional proppants like sand and may produce fewer fines that reduce fluid flow through proppant packs.

Abstract: Proppant particulates like sand are commonly used in hydraulic fracturing operations to maintain one or more fractures in an opened state following the release of hydraulic pressure. Fracturing fluids and methods of hydraulic fracturing may also use proppant particulates composed of fluid coke material (also referred to as fluid coke proppant particulates). In some instances, the fluid coke proppant particulates are characterized by a bulk density of less than about 0.9 grams per cubic centimeter.

Abstract: An absorbent for the selective removal of hydrogen sulfide from a fluid stream comprising carbon dioxide and hydrogen sulfide, wherein the absorbent contains an aqueous solution, comprising: a) an amine or a mixture of amines of the general formula (I) wherein R1 is C1-C5-alkyl; R2 is C1-C5-alkyl; R3 is selected from hydrogen and C1-C5-alkyl; x is an integer from 2 to 10; and b) an ether or a mixture of ethers of the general formula (II): R4—[O—CH2—CH2]y—OH; wherein R4 is C1-C5-alkyl; and y is an integer from 2 to 10; wherein R1 and R4 are identical; wherein the mass ratio of b) to a) is from 0.08 to 0.5. The absorbent is suitable for the selective removal of hydrogen sulfide from a fluid stream comprising carbon dioxide and hydrogen sulfide. The absorbent has a reduced tendency for phase separation at temperatures falling within the usual range of regeneration temperatures for the aqueous amine mixtures and is easily obtainable.

Abstract: A process for removing acid gases from a fluid stream, wherein the fluid stream is contacted with an absorbent comprising a compound of the general formula (I), wherein R1 and R2 are independently C1-C4-alkyl; R3 is selected from hydrogen and C1-C4-alkyl, R4, R5 and R6 are independently selected from hydrogen and C1-C4-alkyl; x and y are integers from 2 to 4 and z is an integer from 1 to 3, to obtain a treated fluid stream and a laden absorbent. The process allows for a high cyclic capacity while the compounds of the absorbent have a reduced tendency to foaming and low volatility.

Abstract: 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.

Abstract: A process for removing acid gases from a fluid stream, wherein the fluid stream is contacted with an absorbent comprising a compound of the general formula (I), wherein R1 and R2 are independently C1-C4-alkyl; R3 is selected from hydrogen and C1-C4-alkyl, R4, R5 and R6 are independently selected from hydrogen and C1-C4-alkyl; x and y are integers from 2 to 4 and z is an integer from 1 to 3, to obtain a treated fluid stream and a laden absorbent. The process allows for a high cyclic capacity while the compounds of the absorbent have a reduced tendency to foaming and low volatility.

Abstract: A system and process for selectively separating H2S from a gas mixture which also comprises CO2 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 H2S selectivity at lower acid gas loadings, and a more dilute absorbent below the recycle feed and having a greater H2S selectivity at higher acid gas loadings. Also disclosed is a system and process for selectively separating H2S by utilizing two different absorbents, one absorbent for the upper section of the absorber, tailored to have a greater H2S selectivity at lower acid gas loadings, and a second absorbent for the lower section of the absorber, tailored to have a greater H2S selectivity at higher acid gas loadings.

Abstract: A delayed coking process in which shot coke and thermally cracked coker products are produced from a sponge coke- and/or transition coke-forming resid feed comprising sponge coke asphaltenes by mixing heteroatom (preferably nitrogen) containing asphaltenes from a shot coke-forming resid with a heated sponge coke-forming resid to form shot coke directing asphaltene aggregates in the resid. The mixture of resid with the added asphaltene is held at an elevated temperature to allow co-aggregates of sponge coke and shot coke asphaltenes to form which, upon delayed coking promote the production of a free-flowing shot coke product.

Abstract: A process for selectively separating H2S from a gas mixture which also comprises CO2 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 H2S/CO2 selectivity of the absorbent solution is preferably greater than about 4.0 for an acid gas loading [mol(CO2+H2S)/mol(amine)] between about 0.2 and about 0.6, and is achieved by reducing pH of the absorbent solution.

Abstract: A process for selectively separating H2S from a gas mixture which also comprises CO2 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 H2S/CO2 selectivity of the absorbent solution is preferably greater than about 4.0 for an acid gas loading [mol(CO2+H2S)/mol(amine)] between about 0.2 and about 0.6, and is achieved by reducing pH of the absorbent solution.

Abstract: A system and process for selectively separating H2S from a gas mixture which also comprises CO2 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 H2S selectivity at lower acid gas loadings, and a more dilute absorbent below the recycle feed and having a greater H2S selectivity at higher acid gas loadings. Also disclosed is a system and process for selectively separating H2S by utilizing two different absorbents, one absorbent for the upper section of the absorber, tailored to have a greater H2S selectivity at lower acid gas loadings, and a second absorbent for the lower section of the absorber, tailored to have a greater H2S selectivity at higher acid gas loadings.

Abstract: A method is described for separating CO2 and/or H2S from a mixed gas stream by contacting the gas stream with a non-aqueous, liquid absorbent medium of a primary and/or secondary aliphatic amine, preferably in a non-aqueous, polar, aprotic solvent under conditions sufficient for sorption of at least some of the CO2. The solution containing the absorbed CO2 can then be treated to desorb the acid gas. The method is usually operated as a continuous cyclic sorption-desorption process, with the sorption being carried out in a sorption zone where a circulating stream of the liquid absorbent contacts the gas stream to form a CO2-rich sorbed solution, which is then cycled to a regeneration zone for desorption of the CO2 (advantageously at <100° C.). Upon CO2 release, the regenerated lean solution can be recycled to the sorption tower. CO2:(primary+secondary amine) adsorption molar ratios>0.5:1 (approaching 1:1) may be achieved.

Abstract: Promoter amines are used to enhance CO2 uptake by sterically hindered or tertiary amines. The promoter amines can be cyclic amines, including aromatic cyclic amines or bridged cyclic amines. The combination of a promoter amine plus a sterically hindered or tertiary amines allows for improved uptake kinetics while reducing or minimizing the amount of formation of carbamate salts. The promoted sterically hindered or tertiary amines can be used as part of a CO2 capture and release system that involves a phase transition from a solution of amine-CO2 products to a slurry of amine-CO2 precipitate solids.