Patent classifications
B01D53/508
Systems and method for removal of acid gas in a circulating dry scrubber
Systems and methods for the use of highly reactive hydrated lime (HRH) in circulating dry scrubbers (CDS) to remove sulfur dioxide (SO.sub.2) from the flue gas.
A PROCESS FOR THE OXIDATION OF HYDROGEN SULFIDE TO SULFUR TRIOXIDE WITH SUBSEQUENT SULFUR REMOVAL AND A PLANT FOR CARRYING OUT THE PROCESS
A process for the oxidation of hydrogen sulfide to sulfur trioxide with subsequent sulfur trioxide removal comprises oxidizing hydrogen sulfide to sulfur trioxide in at least one catalyst-containing reactor and feeding the effluent from the last reactor to a candle filter unit for SO.sub.3 removal, where it is mixed with an injected alkaline sorbent slurry or powder to form an alkali sulfate and a hot clean gas. Preferably the oxidation is done in two reactors, the first oxidizing H.sub.2S to SO.sub.2 over a monolith type catalyst and the second oxidizing SO.sub.2 to SO.sub.3 over a VK type catalyst.
Process for Manufacturing A Sorbent for a Flue Gas Treatment Process, Sorbent and Use of Said Sorbent in Such Flue Gas Treatment Process
The present invention is related to a process for manufacturing a sorbent suitable for a use in a circulating dry scrubber device comprising the steps of: providing quicklime and water in an hydrator; slaking said quicklime via a non-wet route in the hydrator; collecting a lime based sorbent at an exit of the hydrator. The process is characterized in that it comprises a further step of adding at least a first additive comprising: a compound comprising silicon, and/or, a compound comprising aluminum, and/or a compound comprising silicon and aluminum before or during said slaking step, at a molar ratio between silicon or aluminum or a combination thereof and the calcium provided to said hydrator equal to or below 0.2 and equal to or above 0.02. In some other aspects, the present invention is related to a sorbent, a premix, and a flue gas treatment process.
Catalytic adsorbents obtained from municipal sludges, industrial sludges, compost and tobacco waste and process for their production
Industrial waste derived adsorbents were obtained by pyrolysis of sewage sludge, metal sludge, waste oil sludge and tobacco waste in some combination. The materials were used as media to remove hydrogen sulfide at room temperature in the presence of moisture. The initial and exhausted adsorbents after the breakthrough tests were characterized using sorption of nitrogen, thermal analysis, XRD, ICP, and surface pH measurements. Mixing tobacco and sludges result in a strong synergy enhancing the catalytic properties of adsorbents. During pyrolysis new mineral phases are formed as a result of solid state reaction between the components of the sludges. High temperature of pyrolysis is beneficial for the adsorbents due to the enhanced activation of carbonaceous phase and chemical stabilization of inorganic phase. Samples obtained at low temperature are sensitive to water, which deactivates their catalytic centers.
Rechargeable Battery Assembly for a Vehicle
A rechargeable battery assembly for a vehicle has a metal-air rechargeable battery and a filter device to condition inlet air supplied to the metal-air rechargeable battery such that the inlet air exhibits predetermined inlet air values. The filter device has one or more filter elements, one or more sensor devices that determine at least one inlet air parameter, and one or more valve devices. A control system is coupled to the sensor devices so as to receive sensor signals for the at least one inlet air parameter and is coupled to the valve devices. The control system adjusts, depending on the received sensor signals, the valve devices in order to control the predetermined inlet air value in that the inlet air is guided through the filter elements; is guided past the filter elements; or is guided to an air outlet for regenerating the filter elements.
SYSTEM AND METHOD FOR IMPROVING THE PERFORMANCE OF A SELECTIVE CATALYST REDUCTION SYSTEM IN A HEAT RECOVERY STEAM GENERATOR
A heat recovery steam generator includes a gas inlet for receiving a flow of exhaust gas from a gas turbine, a gas outlet opposite the gas inlet and configured to transport the flow of exhaust gas to atmosphere, and a sorbent injection device intermediate the gas inlet and the gas outlet, the sorbent injection device including at least one injection port configured to inject a sorbent into the flow of exhaust gas. The sorbent is configured to react with an acid gas within the flow of exhaust gas to neutralize the acid gas and inhibit the formation of salt deposits.
METHOD FOR DESULPHURIZATING AND DENITRATING FLUE GAS IN INTEGRATED MANNER BASED ON LOW-TEMPERATURE ADSORPTION
Provided is a method for desulphurizating and denitrating a flue gas in an integrated manner based on low-temperature adsorption. The method includes: decreasing a temperature of the flue gas below a room temperature by using a flue gas cooling system; removing moisture in the flue gas by using a dehumidification system; sending the flue gas to a SO.sub.2 and NO.sub.x adsorbing column system; and simultaneously adsorbing SO.sub.2 and NO.sub.x of the flue gas with a material of activated coke, activated carbon, a molecular sieve or diatom mud in the SO.sub.2 and NO.sub.x adsorbing column system to implement an integration of desulphurization and denitration of the flue gas based on the low-temperature adsorption. With the present method, SO.sub.2 and NO.sub.x of the flue gas can be adsorbed simultaneously in an environment having a temperature below the room temperature.
METAL SULFIDES ON ALKALI EARTH PARTICLE SUBSTRATES
The present disclosure relates to methods for producing metal sulfide disposed on particle substrates. In at least one embodiment, a method for producing an alkali earth hydroxide particle having a metal sulfide disposed thereon includes introducing an alkali earth oxide particle with a metal sulfate to form a first composition. The method includes introducing an alkali sulfide or an alkali earth sulfide with the first composition to form a second composition. The present disclosure further relates to compositions of matter having metal sulfide disposed on a particle substrate. In at least one embodiment, a composition of matter includes an alkali earth hydroxide particle. The composition of matter includes a metal sulfide disposed on the alkali earth hydroxide particle.
Electrostatic precipitator module and desulfurization system including the same
An electrostatic precipitator module and a desulfurization system are capable of easily discharging wash water from a wet electrostatic precipitator module. The electrostatic precipitator module includes an arrangement of discharge electrodes and collecting electrodes alternately disposed and spaced apart from each other, the discharge electrodes configured to be charged to a predetermined voltage for generating a corona discharge between the discharge electrodes and the collecting electrodes; and tie rods for fixing the discharge electrodes and the collecting electrodes. Each collecting electrode has a lower edge inclined downward with respect to the ground. The lower edge of each collecting electrode includes separate lower edge portions respectively inclined downward from opposite side ends of the collecting electrode and a lowermost point at which wash water is concentrated and discharged to a discharge guide installed directly under the lowermost points. The discharge guide has a width substantially smaller than the collecting electrode.
Low pressure drop static mixing system
A contaminated gas stream can be passed through an in-line mixing device, positioned in a duct containing the contaminated gas stream, to form a turbulent contaminated gas stream. One or more of the following is true: (a) a width of the in-line mixing device is no more than about 75% of a width of the duct at the position of the in-line mixing device; (b) a height of the in-line mixing device is no more than about 75% of a height of the duct at the position of the in-line mixing device; and (c) a cross-sectional area of the mixing device normal to a direction of gas flow is no more than about 75% of a cross-sectional area of the duct at the position of the in-line mixing device. An additive can be introduced into the contaminated gas stream to cause the removal of the contaminant by a particulate control device.