An improved process for deacidizing a gaseous mixture with reduced overall energy costs is described. The process involves contacting the gaseous mixture with at least one of a vaporizing compound, a vaporized compound, a vaporizing solution of compound and a vaporized solution of compound, and forming a liquid or solid reaction product that can be easily separated from the gaseous mixture.

A system for carbon dioxide capture from a gas mixture comprises an absorber that receives a lean solvent system stream (containing a chemical solvent, physical-solvent additive, and water) from the stripper, a stripper that receives the rich solvent stream from the absorber and produces the product carbon dioxide and the lean solvent through the use of a reboiler in fluid communication with a lower portion of the stripper, a condenser in fluid communication with a vapor outlet of the stripper, a cross-exchanger in fluid communication with a rich solvent system outlet from the absorber and a rich solvent system inlet on the stripper, and a splitter. The splitter is configured to separate the rich solvent system stream into a first portion and a second portion, where the first portion directly passes to the stripper and the second portion passes through the cross-exchanger prior to passing to the stripper.

A system for containing an emission of sulfur trioxide, the system comprising a first pressurized vessel, the first pressurized vessel containing sulfur trioxide, a relief vessel containing a volume of a solvent solution, wherein the solvent solution comprises sulfolane, and a first relief conduit providing a first route of fluid communication between the first pressurized vessel and the relief vessel. A method for containing an emission of sulfur trioxide, the method comprising routing a first relief conduit so as to provide a first route of fluid communication between a first pressurized vessel and a relief vessel, wherein the first pressurized vessel contains sulfur trioxide, wherein the relief vessel contains a volume of a solvent solution, and wherein the solvent solution comprises sulfolane.

A carbon dioxide absorbent composition is described, including (i) a liquid, nonaqueous silicon-based material, functionalized with one or more groups that either reversibly react with CO.sub.2 or have a high-affinity for CO.sub.2, and (ii) a hydroxy-containing solvent that is capable of dissolving both the silicon-based material and a reaction product of the silicon-based material and CO.sub.2. The absorbent may be utilized in methods to reduce carbon dioxide in an exhaust gas, and finds particular utility in power plants.

The use of a chemical composition in degassing of vessels is taught, said chemical composition comprising 1-10% by weight of an oxyalkylated dodecyl thiol; and 1-20% by weight of an alkyl di-substituted 9-decenamide. A method is further provided for degassing a vessel. The method comprises charging said vessel with chemical composition and a carrier medium, wherein said chemical composition comprises 1-10% by weight of an oxyalkylated dodecyl thiol and 1-20% by weight of an alkyl di-substituted 9-decenamide.

An improved process for deacidizing a gaseous mixture with reduced overall energy costs is described. The process involves contacting the gaseous mixture with at least one of a vaporizing compound, a vaporized compound, a vaporizing solution of compound and a vaporized solution of compound, and forming a liquid or solid reaction product that can be easily separated from the gaseous mixture.

A system for containing an emission of sulfur trioxide, the system comprising a first pressurized vessel, the first pressurized vessel containing sulfur trioxide, a relief vessel containing a volume of a solvent solution, wherein the solvent solution comprises sulfolane, and a first relief conduit providing a first route of fluid communication between the first pressurized vessel and the relief vessel. A method for containing an emission of sulfur trioxide, the method comprising routing a first relief conduit so as to provide a first route of fluid communication between a first pressurized vessel and a relief vessel, wherein the first pressurized vessel contains sulfur trioxide, wherein the relief vessel contains a volume of a solvent solution, and wherein the solvent solution comprises sulfolane.

The present invention relates generally to the field of emission control equipment for boilers, heaters, kilns, or other flue gas-, or combustion gas-, generating devices (e.g., those located at power plants, processing plants, etc.) and, in particular to a new and useful method and apparatus for: (i) reducing the levels of one or more gas phase selenium compounds and/or one or more other RCRA metals, or RCRA metal compounds (regardless of whether such other RCRA metals or RCRA metal compounds are in the gas phase or some other phase); (ii) capturing, sequestering and/or controlling one or more gas phase selenium compound and/or one or more other RCRA metals, or RCRA metal compounds (regardless of whether such other RCRA metals or RCRA metal compounds are in the gas phase or some other phase) in a flue gas stream and/or in one or more pieces of emission control technology; and/or (iii) capturing, sequestering and/or controlling one or more gas phase selenium compound and/or one or more other RCRA metals, or RCRA metal compounds (regardless of whether such other RCRA metals or RCRA metal compounds are in the gas phase or some other phase) in a flue gas stream prior to desulfurization and/or in one or more pieces of emission control technology prior to one or more desulfurization units,

An aqueous ionic absorbent solution is disclosed containing (a) about 15 wt. % to about 80 wt. % of one or more diluents, based on the total weight of the aqueous ionic absorbent solution; and (b) an ionic absorbent containing a cation and an anion comprising an amine moiety.

A method is described for separating CO.sub.2 and/or H.sub.2S 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 CO.sub.2. The solution containing the absorbed CO.sub.2 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 CO.sub.2-rich sorbed solution, which is then cycled to a regeneration zone for desorption of the CO.sub.2 (advantageously at <100 C.). Upon CO.sub.2 release, the regenerated lean solution can be recycled to the sorption tower. CO.sub.2:(primary+secondary amine) adsorption molar ratios>0.5:1 (approaching 1:1) may be achieved.