Patent classifications
B01D53/48
Apparatus and method for a carbon reduction assembly
A carbon reduction assembly adapted for use with wet and dry coal combustion products (“CCPs”). The assembly includes a direct-fired carbon reduction section having a dry material inlet device that is adapted to receive the dry CCPs and a direct-fired carbon reduction section burner unit that is adapted to reduce carbon content in the dry CCPs. The assembly also includes a direct-fired dryer section that is operatively connected with the direct-fired carbon reduction section and has a wet material inlet device that is adapted to receive the wet CCPs and a direct-fired dryer section drum that is adapted to dry the wet CCPs. The assembly further includes a control unit that is operatively connected with the carbon reduction section and the dryer section. An amount of hot gas generated by the carbon reduction section is conveyed to the dryer section, and the assembly is adapted to produce dry fly ash.
Apparatus and method for a carbon reduction assembly
A carbon reduction assembly adapted for use with wet and dry coal combustion products (“CCPs”). The assembly includes a direct-fired carbon reduction section having a dry material inlet device that is adapted to receive the dry CCPs and a direct-fired carbon reduction section burner unit that is adapted to reduce carbon content in the dry CCPs. The assembly also includes a direct-fired dryer section that is operatively connected with the direct-fired carbon reduction section and has a wet material inlet device that is adapted to receive the wet CCPs and a direct-fired dryer section drum that is adapted to dry the wet CCPs. The assembly further includes a control unit that is operatively connected with the carbon reduction section and the dryer section. An amount of hot gas generated by the carbon reduction section is conveyed to the dryer section, and the assembly is adapted to produce dry fly ash.
Method for controlling gaseous mercury emission between two or more coal-fired combustion units
The present invention relates to coal-fired power plants and flue gas emissions and more specifically, to controlling gaseous mercury emissions in the flue gas between two or more coal fired electric generating units within a contiguous power plant site to achieve environmental regulation limits for mercury emissions. This is accomplished by continuously adjusting the application rates of mercury oxidant, which is added to a coal feed to oxidize elemental mercury for improved mercury capturability and aqueous mercury precipitant (liquid), which is added to a scrubber liquor of a wet Flue Gas Desulfurization (FGD) unit to precipitate out oxidized mercury into solid form for improved capture and disposal.
Method for controlling gaseous mercury emission between two or more coal-fired combustion units
The present invention relates to coal-fired power plants and flue gas emissions and more specifically, to controlling gaseous mercury emissions in the flue gas between two or more coal fired electric generating units within a contiguous power plant site to achieve environmental regulation limits for mercury emissions. This is accomplished by continuously adjusting the application rates of mercury oxidant, which is added to a coal feed to oxidize elemental mercury for improved mercury capturability and aqueous mercury precipitant (liquid), which is added to a scrubber liquor of a wet Flue Gas Desulfurization (FGD) unit to precipitate out oxidized mercury into solid form for improved capture and disposal.
CHEMICAL PROCESS FOR SULFUR REDUCTION OF HYDROCARBONS
Treatment of hydrocarbon streams, and in one non-limiting embodiment refinery distillates, with high pH aqueous reducing agents, such as borohydride, results in reduction of the sulfur compounds such as disulfides, mercaptans and thioethers that are present to give easily removed sulfides. The treatment converts the original sulfur compounds into hydrogen sulfide or low molecular weight mercaptans that can be extracted from the distillate with caustic solutions, hydrogen sulfide or mercaptan scavengers, solid absorbents such as clay or activated carbon or liquid absorbents such as amine-aldehyde condensates and/or aqueous aldehydes.
Apparatus and method for recovering carbon dioxide in combustion exhaust gas
The present invention relates to an apparatus and method for recovering carbon dioxide (hereinafter also referred to as “CO.sub.2”) contained in a combustion exhaust gas, and more specifically relates to: an apparatus and method for reactively absorbing CO.sub.2 contained in a combustion exhaust gas into an amine compound-containing absorption liquid; an apparatus and method for desorbing CO.sub.2 contained in an amine compound-containing absorption liquid from the amine compound-containing absorption liquid; an apparatus and method for evaporating and separating impurities from the amine compound-containing absorption liquid containing the impurities; an apparatus and method for performing a pretreatment such as desulfurization, dust removal, and cooling on a combustion exhaust gas; and a carbon dioxide-recovering apparatus and method utilizing the above apparatuses and methods.
Material such as film, fiber, woven and nonwoven fabric with adsorbancy
Compositions that can be used to adsorb low concentration, of unwanted or target substances from a dynamic fluid stream or from an enclosed static vapor phase. Such adsorbency can be obtained with thermoplastic materials used in the form of bulk polymer or a film, fiber, web, woven fabric, non-woven fabric, sheet, packaging and other such structures including or surrounding the enclosed volume. The concentration should be reduced to non-offensive sensed limits or a limit that does not produce a biological response.
Material such as film, fiber, woven and nonwoven fabric with adsorbancy
Compositions that can be used to adsorb low concentration, of unwanted or target substances from a dynamic fluid stream or from an enclosed static vapor phase. Such adsorbency can be obtained with thermoplastic materials used in the form of bulk polymer or a film, fiber, web, woven fabric, non-woven fabric, sheet, packaging and other such structures including or surrounding the enclosed volume. The concentration should be reduced to non-offensive sensed limits or a limit that does not produce a biological response.
Catalyst for the oxidation of sulfur compounds
In a broad form the present invention relates to a method for oxidation of a species comprising sulfur in an oxidation state below +4, such as H.sub.2S, CS.sub.2, COS and S.sub.8 vapor, to SO.sub.2 said method comprising the step of contacting the gas and an oxidant with a catalytically active material consisting of one or more elements taken from the group consisting of V, W, Ce, Mo, Fe, Ca, Mg, Si, Ti and Al in elemental, oxide, carbide or sulfide form, optionally with the presence of other elements in a concentration below 1 wt %, at a temperature between 180° C. and 290° C., 330° C., 360° C. or 450° C., with the associated benefit of such a temperature being highly energy effective, and the benefit of said elements having a low tendency to form sulfates under the conditions, with the related benefit of an increased stability of the catalytically active material. The other elements present may be catalytically active noble metals or impurities in the listed materials.
Method for preparing solids from a mixture of at least one malachite powder and an oxide powder and the use of said solids
The invention relates to a method for preparing a solid comprising the mixture of a set of compounds comprising at least one Cu.sub.2(OH).sub.2CO.sub.3 powder, one metal oxide powder selected from the group of metals consisting of copper, zinc, iron, manganese and mixtures thereof, and at least one binder as well as the use of the solid prepared by means of this method.