There is an absorbent mixture usable for the removal of sour gases from gas mixtures. The mixture has at least one organic base having a pK.sub.b (in water) less than or equal to 3.2; at least one alcoholic solvent of general formula R(OH).sub.n having a boiling temperature above or equal to 100° C. at ambient pressure, wherein R is a linear or branched saturated alkyl group having a number of carbon atoms between 2 and 20 and n is a whole number varying between 1 and 20; an aprotic polar solvent having a dielectric constant ε at 25° C. greater than or equal to 30, a viscosity μ at 25° C. less than or equal to 14 cP, preferably less than or equal to 12 cP; and a boiling temperature at normal pressure equal to or above 130° C. There is also a process for the removal of sour gases using the absorbent mixture.

Disclosed are a flue gas purification and waste heat utilization system and method. The system comprises a flue gas exhaust unit, a primary waste heat utilization unit, a primary flue gas purification unit, a secondary waste heat utilization unit and a secondary flue gas purification unit that are sequentially connected in a flue gas flow direction, wherein the primary flue gas purification unit is configured for removing NO.sub.x, large particles and CO in the flue gas, the secondary flue gas purification unit is configured for removing NO.sub.x and dioxin in the flue gas, an ammonia-spraying device is externally connected between the flue gas exhaust unit and the primary waste heat utilization unit, and the ammonia-spraying device is configured for injecting ammonia gas into the flue gas exhausted from the flue gas exhaust unit.

Absorption, or gas absorption, is a unit operation used in the chemical industries to separate gases by washing or scrubbing a gas mixture with a suitable liquid. Gas absorption is usually carried out in vertical countercurrent columns The solvent is fed in at the top of the absorber, the gas mixture from the bottom. We developed the process to get high yield and high efficiency.

Sorptive gas separators can employ contactors having various sorbents blended together. The various sorbents used to make a blended sorbent contactor can be selected for their various physical and chemical properties, which will allow operators to customize formulations and structural configurations to obtain optimum performance of sorptive gas separators using blended sorbents.

Disclosed are a CHA zeolite membrane and a method of preparing the same, and more particularly, a CHA zeolite membrane having high capacity to separate CO.sub.2/N.sub.2 and CO.sub.2/CH.sub.4 even under wet conditions using a membrane produced using a synthetic precursor having a controlled ratio of Si and Al, a method of preparing the same, and a method of capturing and removing carbon dioxide using the membrane.

The present invention provides environmental equipment which is able to remarkably reduce operating costs and a power generation system comprising same, comprising: a boiler; a power generation unit for generating electricity by steam generated from the boiler; first denitrifying equipment to which exhaust gas is delivered from the boiler and which sprays a reducing agent into the exhaust gas to denitrify the exhaust gas; a low-low temperature electrostatic precipitator for collecting dust of the exhaust gas provided from the first denitrifying equipment; second denitrifying equipment which sprays a reducing agent into the exhaust gas provided from the low-low temperature electrostatic precipitator to secondarily denitrify the exhaust gas and allows the exhaust gas to be provided towards a smokestack.

The present invention pertains to: a vanadium pentoxide-tungsten trioxide catalyst supported on an iron ion-exchanged titanium dioxide; and a method for removing nitrogen oxides using the same. More specifically, the present invention pertains to: a deNO.sub.xing catalyst in which the iron ion-exchanged titanium dioxide is utilized as a support for the vanadium pentoxide and tungsten trioxide to drastically reduce the generation and emission of nitrous oxide; and a method for removing nitrogen oxides using the same.

The sodium ferrite particle powder according to the present invention is characterized in that at least one metal or more selected from the metal group consisting of silicon, aluminum, titanium, manganese, cobalt, nickel, magnesium, copper and zinc is contained in an amount of 0.05 to 20% by weight in terms of the oxide, and the molar ratio of Na/Fe is 0.75 to 1.25.

This exhaust gas processing equipment is provided with an exhaust line through which exhaust gas discharged from a boiler circulates, a carbon dioxide recovering device for recovering carbon dioxide included in the exhaust gas, and an exhaust gas heating device provided downstream of the carbon dioxide recovering device to heat the exhaust gas. The carbon dioxide recovering device includes a first medium line through which a first medium circulates, and a second medium line through which a second medium higher in temperature than the first medium circulates. The exhaust gas heating device includes a first heating unit for heating the exhaust gas by means of heat exchange with the first medium, and a second heating unit for heating the exhaust gas passing through the first heating unit even more by heat exchange with the second medium.

A method of heating a fluid stream for a power plant comprises diverting a portion of a main flow of flue gas from a power plant at a first pressure (P1), flowing the diverted flue gas through a heat exchanger, flowing an auxiliary fluid stream through the heat exchanger, and transferring heat from the diverted flue gas into the auxiliary fluid stream in the heat exchanger to raise a temperature of the auxiliary fluid stream from a first temperature (T3) to a second temperature (T4), while lowering a first temperature of the diverted flue gas (T1) to a second temperature (T2). The diverted flue gas is then returned to the main flow of flue gas in the power plant at a second pressure (P2). The method of flue gas flow through the heat exchanger may be accomplished by adding a self-contained flow path from a boiler higher pressure (P1) zone to a lower pressure (P2) zone.