Patent classifications
B01D53/78
SYSTEM AND METHOD FOR DESULFURIZING AND DECARBONIZING FLUE GAS
A method for desulfurizing and decarbonizing a flue gas includes: feeding a boiler flue gas after denitrating and dedusting to a water cooler; cooling the boiler flue gas in the water cooler to a temperature near room temperature, and discharging condensed water; feeding a wet flue gas to a washing tower; washing and cooling the wet flue gas with a washing liquid to separate H.sub.2O, SO.sub.2 and CO.sub.2 in a solid form from the flue gas; feeding a solid-liquid mixed slurry from a bottom of the washing tower to a solid-liquid separator to separate solid H.sub.2O, SO.sub.2 and CO.sub.2 from the washing liquid; feeding the solid H.sub.2O, SO.sub.2 and CO.sub.2 to a rectification separation column; separating CO.sub.2 from SO.sub.2 and H.sub.2O by a reboiler at a bottom of the rectification separation column; and discharging CO.sub.2, SO.sub.2 and H.sub.2O.
SYSTEM AND METHOD FOR DESULFURIZING AND DECARBONIZING FLUE GAS
A method for desulfurizing and decarbonizing a flue gas includes: feeding a boiler flue gas after denitrating and dedusting to a water cooler; cooling the boiler flue gas in the water cooler to a temperature near room temperature, and discharging condensed water; feeding a wet flue gas to a washing tower; washing and cooling the wet flue gas with a washing liquid to separate H.sub.2O, SO.sub.2 and CO.sub.2 in a solid form from the flue gas; feeding a solid-liquid mixed slurry from a bottom of the washing tower to a solid-liquid separator to separate solid H.sub.2O, SO.sub.2 and CO.sub.2 from the washing liquid; feeding the solid H.sub.2O, SO.sub.2 and CO.sub.2 to a rectification separation column; separating CO.sub.2 from SO.sub.2 and H.sub.2O by a reboiler at a bottom of the rectification separation column; and discharging CO.sub.2, SO.sub.2 and H.sub.2O.
METHOD FOR FIXING CARBON DIOXIDE, METHOD FOR PRODUCING FIXED CARBON DIOXIDE, AND CARBON DIOXIDE FIXATION APPARATUS
The present invention provides a new method for fixing carbon dioxide. The method for fixing carbon dioxide of the present invention, includes: a contact step of bringing a mixed liquid containing sodium hydroxide and further containing at least one of a chloride of a Group 2 element or a chloride of a divalent metal element into contact with a gas containing carbon dioxide, wherein in the contact step, the mixed liquid and the gas are brought into contact with each other by feeding the gas into the mixed liquid, a concentration of the sodium hydroxide in the mixed liquid is 0.01 N or more and 0.2 N or less, and in the contact step, the feeding is performed by a motor-driven pump, and the motor is driven by utilizing power generated by photovoltaic power generation.
METHOD FOR FIXING CARBON DIOXIDE, METHOD FOR PRODUCING FIXED CARBON DIOXIDE, AND CARBON DIOXIDE FIXATION APPARATUS
The present invention provides a new method for fixing carbon dioxide. The method for fixing carbon dioxide of the present invention, includes: a contact step of bringing a mixed liquid containing sodium hydroxide and further containing at least one of a chloride of a Group 2 element or a chloride of a divalent metal element into contact with a gas containing carbon dioxide, wherein in the contact step, the mixed liquid and the gas are brought into contact with each other by feeding the gas into the mixed liquid, a concentration of the sodium hydroxide in the mixed liquid is 0.01 N or more and 0.2 N or less, and in the contact step, the feeding is performed by a motor-driven pump, and the motor is driven by utilizing power generated by photovoltaic power generation.
PRODUCTION METHOD FOR HIGH-PURITY HYDROGEN CHLORIDE GAS
A method for producing a high-purity hydrogen chloride gas comprises performing a purification process that includes the steps 1) to 3) below on a byproduct hydrogen chloride gas: 1) a crude hydrochloric acid generation step of allowing water to absorb the byproduct hydrogen chloride gas; 2) a volatile organic impurity-removed hydrochloric acid generation step of bringing the crude hydrochloric acid obtained in the step 1) into contact with an inert gas at a liquid temperature of 20 to 45° C. to dissipate volatile organic impurities; and 3) a high-purity hydrogen chloride gas generation step of supplying the volatile organic impurity-removed hydrochloric acid obtained in the step 2) to a distillation column and performing distillation under conditions of a column bottom temperature of higher than 60° C. and 108° C. or lower and a column top temperature of 60° C. or lower to distill out a high-purity hydrogen chloride gas.
CHEMICAL COMPOSITIONS AND METHODS OF USING SAME FOR REMEDIATING SULFUR-CONTAINING COMPOSITIONS AND OTHER CONTAMINANTS IN FLUIDS
A treatment process for remediating; contaminants in a mixture of contaminated fluids, including at least one liquid fluid and at least one gaseous fluid, includes the steps of: preparing a treatment composition containing at least 80 volume % of an aqueous solution containing at least one hydroxide compound at a collective concentration of 35-55 weight percent, and at least one organic acid selected from the group consisting of fulvic acid and humic acid at a collective concentration of 0.1-5 wt % of the treatment composition; adding a dosage of the treatment composition to a mixture of contaminated fluids including a liquid portion and a gaseous portion; and allowing the treatment composition to react with the mixture of contaminated fluids for at least 10 minutes. A pH of the treatment composition is at least 12.0
CHEMICAL COMPOSITIONS AND METHODS OF USING SAME FOR REMEDIATING SULFUR-CONTAINING COMPOSITIONS AND OTHER CONTAMINANTS IN FLUIDS
A treatment process for remediating; contaminants in a mixture of contaminated fluids, including at least one liquid fluid and at least one gaseous fluid, includes the steps of: preparing a treatment composition containing at least 80 volume % of an aqueous solution containing at least one hydroxide compound at a collective concentration of 35-55 weight percent, and at least one organic acid selected from the group consisting of fulvic acid and humic acid at a collective concentration of 0.1-5 wt % of the treatment composition; adding a dosage of the treatment composition to a mixture of contaminated fluids including a liquid portion and a gaseous portion; and allowing the treatment composition to react with the mixture of contaminated fluids for at least 10 minutes. A pH of the treatment composition is at least 12.0
Sulfur recovery within a gas processing system
A method for recovering sulfur within a gas processing system is described herein. The method includes contacting a natural gas stream including an acid gas with a solvent stream within a co-current contacting system to produce a sweetened natural gas stream and a rich solvent stream including an absorbed acid gas. The method also includes removing the absorbed acid gas from the rich solvent stream within a regenerator to produce a concentrated acid gas stream and a lean solvent stream. The method further includes recovering elemental sulfur from hydrogen sulfide (H.sub.2S) within the concentrated acid gas stream via a sulfur recovery unit.
Sulfur recovery within a gas processing system
A method for recovering sulfur within a gas processing system is described herein. The method includes contacting a natural gas stream including an acid gas with a solvent stream within a co-current contacting system to produce a sweetened natural gas stream and a rich solvent stream including an absorbed acid gas. The method also includes removing the absorbed acid gas from the rich solvent stream within a regenerator to produce a concentrated acid gas stream and a lean solvent stream. The method further includes recovering elemental sulfur from hydrogen sulfide (H.sub.2S) within the concentrated acid gas stream via a sulfur recovery unit.
HYDROGEN SULFIDE REMOVAL PROCESS
A process is presented to treat a process gas stream containing hydrogen sulfide using a reverse jet absorber with a liquid treatment solution containing a chelated metal catalyst. A treat gas substantially free of the hydrogen sulfide is separated from a spent liquid treatment solution containing elemental sulfur which can then be regenerated in an oxidation vessel where it is contacted with an oxygen containing gas to convert the spent liquid treatment solution to a regenerated liquid treatment solution that can be recycled for introduction into the reverse jet absorber.