Patent classifications
B01D53/8609
METHOD FOR DESULFURIZATION OF SELECTIVE CATALYTIC REDUCTION DEVICES
Described herein is a desulfurization method for desulfurizing a SCR device treating an exhaust gas. The desulfurization method includes injecting a reductant into the exhaust gas upstream from or into the SCR device and increasing a temperature of the exhaust gas.
Marine engine pretreatment desulfurization control and monitoring system
The present invention includes a fuel injection amount sensor for detecting an injection amount of oil, a pretreatment desulfurization agent injection amount sensor for detecting an injection amount of a pretreatment desulfurization agent, and a control panel for controlling and monitoring the injection amount of the pretreatment desulfurization agent so that the predetermined desulfurization agent is mixed with the fuel in a predetermined mixing ratio. The fuel injection amount sensor is disposed on a fuel supply line between a fuel tank and a marine engine, and the pretreatment desulfurization agent injection amount sensor is disposed between a downstream fuel supply line installed downstream of the fuel injection amount sensor and a pretreatment desulfurization agent tank.
Clean Gas Stack
A flow-through solid catalyst formed by coating a zeolite material on a metal or ceramic solid substrate. In some embodiments, the solid substrate is formed as flat plates, corrugated plates, or honeycomb blocks.
Process and apparatus for reducing acid plume
The description relates to a process for reducing acid plume from stacks from coal-fired combustors operating at varying loads, which have typically been treated by back-end calcium carbonate (limestone) which has not been able to effectively control visible acid plume as power is ramped up from low load. According to the process, as high sulfur and high iron coals are burned in a combustor, magnesium hydroxide slurry is introduced into hot combustion gases in or near the combustion zone. And, during ramp up to high load from a period of operation at low load, additional magnesium hydroxide is introduced into an intermediate-temperature zone.
EMISSIONS CONTROL SYSTEM INCLUDING CAPABILITY TO CLEAN AND/OR REJUVENATE CARBON-BASED SORBENTS AND METHOD OF USE
A system and method for cleaning, conditioning, and/or rejuvenating carbon-based sorbents is disclosed where a chemical cleaning process is used to separate contaminants from the sorbent. The contaminants can be disposed of or recycled for industrial uses. The cleaned and/or rejuvenated carbon-based sorbent is recycled back into a reverse venturi shaped fluidized bed apparatus for later use. Spent carbon-based sorbent can be routed for appropriate disposal. The carbon-based sorbents include, but are not limited to, activated carbon sorbent and biochar sorbent. Optionally, the sorbents can be processed through the system prior to exposure to contaminated emissions to enhance and increase the porosity of the outer surface of the sorbents.
EMISSIONS CONTROL SYSTEM INCLUDING CAPABILITY TO CLEAN AND/OR REJUVENATE CZTS SORBENTS, CZTS-ALLOY SORBENTS, AND/OR CZTS-MIXTURE SORBENTS, AND METHOD OF USE
An emissions control system including a fluidized bed apparatus containing a reactive sorbent material is disclosed for gaseous and non-gaseous contaminated emissions. The reactive sorbent material may be CZTS, CZTS-Alloy, or a CZTS-Mixture sorbent material. The fluidized bed apparatus is configured with one or more closed loop sorbent recycling subsystems. The sorbent recycling subsystems include the capability to separate sorbents from each other, separate contaminates from sorbents for disposal and/or recycling, clean and/or rejuvenate sorbents for return to the fluidized bed apparatus, dispose of spent and exhausted sorbents, and replace the spent and exhausted sorbents with new sorbent to maintain consistent sorbent function in the fluidized bed apparatus. Monitoring sensors provide information useful in a method for establishing and maintaining consistent process parameter controls.
Catalyst for catalytic reduction of industrial flue gas SO.SUB.2 .with CO to prepare sulfur, method for preparing same and use thereof
The present invention provides a catalyst for catalytic reduction of an industrial flue gas SO.sub.2 with CO to prepare sulfur, a method for preparing the same and use thereof. A CeO.sub.2 nanocarrier is prepared by using a hydrothermal method, La and Y are loaded as active components, pre-sulfurization is conducted with 6% of SO.sub.2 and 3% of CO, and finally, the catalyst is prepared. The catalyst has high reactivity and sulfur selectivity and strong stability. The by-product sulfur generated by the reaction is recovered with a solvent CS.sub.2, and the solvent CS.sub.2 is recovered by using a distillation process. The preparation method is low in cost, causes no secondary pollution and is high in sulfur recovery rate. The problem of low sulfur production in China at present is solved.
Catalyst for use in the catalytic reduction of sulfur contained in a gas stream and method of making and using such catalyst
Presented is a catalyst composition having exceptional properties for converting sulfur, sulfur compounds, and carbon monoxide contained in gas streams by catalyzed hydrolysis, hydrogenation and water-gas shift reactions. The catalyst comprises underbedded molybdenum and cobalt with an overlayer of molybdenum and cobalt. These metals are present in the catalyst within certain concentration ranges and relative weight ratios. The underbedded metals are present in the catalyst within a specified range relative to the overlayer and total metals. The underbedded metals are formed by co-mulling an inorganic oxide with the catalytically active metals of molybdenum and cobalt. The co-mulled mixture is calcined and then impregnated with overlaid molybdenum and cobalt.
Method for the catalytic removal of sulphur dioxide from waste gases
The present invention relates to a method for the catalytic removal of sulfur dioxide from waste gases in two reactors, wherein the first reactor is charged with an activated carbon catalyst. The method comprises: a. provision of a waste gas with a water content of less than 1 g H.sub.2O/Nm.sup.3 and an SO.sub.2 content of at least 5 ppm, b. introduction of the waste gases into a first reactor, c. catalytic conversion of the SO.sub.2 into gaseous SO.sub.3 in the first reactor by the activated carbon catalyst, wherein catalytic conversion on the activated carbon catalyst proceeds at a temperature of below 100 C., d. introduction of the prepurified waste gases from the first reactor into a second reactor, e. conversion of the SO.sub.3 with water into H.sub.2SO.sub.4 in the second reactor.
Hydrophobic filtration of tempering air
A gas turbine system may include an exhaust gas processing system configured to process exhaust gas received from a gas turbine engine of the system. An exhaust path of the exhaust processing system is configured to flow the exhaust gas through the exhaust processing system. A tempering air system of the exhaust processing system is configured to introduce tempering air into the exhaust path to cool the exhaust gas. The tempering air system includes a tempering air pathway extending from an air inlet of the tempering air system to a tempering air outlet where tempering air is introduced from the tempering air system and into the exhaust path. A filter system of the tempering air system has a hydrophobic filter positioned along the tempering air pathway, the hydrophobic filter being configured to remove hygroscopic and deliquescent materials from the air flowing through the tempering air pathway.