Abstract: A system for reducing ammonia (NH3) emissions includes (a) a first component comprising a first substrate containing a three-way catalyst, wherein the first component is disposed upstream of a second component comprising a second substrate containing an ammonia oxidation catalyst, wherein said ammonia oxidation catalyst comprises a small pore molecular sieve supporting at least one transition metal; and (b) an oxygen-containing gas input disposed between the components. For example, a CHA Framework Type small pore molecular sieve may be used. A method for reducing NH3 emission includes introducing an oxygen-containing gas into a gas stream to produce an oxygenated gas stream; and exposing the oxygenated gas stream to an NH3 oxidation catalyst to selectively oxidize at least a portion of the NH3 to N2. The method may further include the step of exposing a rich burn exhaust gas to a three-way catalyst to produce the gas stream comprising NH3.

Abstract: A catalyst includes a platinum coating deposited on a silica support. The support has an average surface area between about 100 m2/g and about 120 m2/g. The platinum coating is between about 5 wt % and about 15 wt % of the catalyst. The combination of the selected surface area, silica support, and selected amount of platinum coating provides a catalytic activation temperature below 200° C. and avoids the formation of NOx.

Abstract: A process for producing a purified synthesis gas stream from a contaminated feed synthesis gas stream is disclosed. A part of the feed synthesis gas stream is subjected to a water gas shift step. The water gas shift step is used in combination with bulk contaminant removal followed by polishing to thereby remove the contaminants from the synthesis gas stream so as to provide the purified synthesis gas stream having a desired low level of contaminants.

Abstract: A method for recovering NH3 present in a sour water stream containing odiferous compounds such as pyridines, indoles, ketones and mercaptans produced during an upgrading process for upgrading bitumen from oil sands into synthetic crude comprising treating the sour water stream in a sour water treatment unit to produce a NH3-rich stream and a H2S-rich stream; and hydrotreating the NH3-rich stream in a hydrotreater in the presence of hydrogen to remove the odiferous compounds such as pyridines, indoles, ketones and mercaptans and produce a treated NH3-rich stream.

Abstract: The present invention relates to a catalyst comprising 0.1-10 mol % Co3-xMxO4, where M is Fe or Al and x=0-2, on a cerium oxide support for decomposition of N2O in gases containing NO. The catalyst may also contain 0.01-2 weight % ZrO2. The invention further comprises a method for performing a process comprising formation of N2O. The N2O containing gas is brought in contact with a catalyst comprising 0.1-10 mol % Co3-xMxO4, where M is Fe or Al and x=0-2, on a cerium oxide support, at 250-1000° C. The method may comprise that ammonia is oxidized in presence of an oxidation catalyst and that the thereby formed gas mixture is brought in contact with the catalyst comprising the cobalt component on cerium oxide support at a temperature of 500-1000° C.

Abstract: A method for the high removal of ammonia, COS and HCN from syngas (along with some polishing of particulates) in a cost effective and environmentally benign and sustainable fashion, with the need for little to no chemical addition by using a combination of water based gas scrubbing, HCN scrubbing and biological processing steps.

Abstract: This invention relates to processes and apparatuses for purifying greenhouse gases. This invention relates to processes and apparatuses for drying carbon dioxide and/or producing syngas. The process includes the step of contacting a greenhouse gas stream having a contaminant with a solvent stream to at least partially reduce an amount of the contaminant and form a used solvent stream. The process includes the step of using the greenhouse gas stream for carbon sequestration, enhanced oil recovery, industrial gas supply, or chemical synthesis and production.

Abstract: The invention relates to a process for determining the total oxygen content and the total carbon content in ammonia, in which ammonia is first split into nitrogen and hydrogen, then the oxygen still present in the ammonia is reacted essentially fully with hydrogen to give water and the carbon still present is reacted essentially fully with hydrogen to give methane. In a next step, the water content and the methane content in the gas are determined. Finally, the total oxygen content is determined from the water content and the total carbon content from the methane content. The invention further relates to an apparatus for performing the process, which comprises a cracker for splitting the ammonia and for converting the oxygen- and/or carbon-comprising compounds, and at least one cavity ring-down spectrometer for detecting the water content and/or carbon content.

Abstract: An apparatus and method for achieving increased NOx removal efficiency from an emissions control portion of a fossil fuel fired boiler while controlling ammonia slip provides excess levels of ammonia above those levels conventionally employed in SCR and/or SNCR applications. The apparatus and methods comprise, in part, use of a NOx reduction system comprising at least one selective catalytic reduction system which receives ammonia in higher amounts than conventional practice from an upstream ammonia injection point, and an ammonia reduction system positioned downstream of one or more ammonia injection points and the NOx reduction system. The excess ammonia achieves increased NOx removal, while the ammonia reduction system contains at least one ammonia destruction catalyst which permits the NOx reduction system to be operated at an increased NOx removal efficiency without a corresponding increase in ammonia slip.

Abstract: A hydrogen generation apparatus employs a thermocatalytic reactor (60) formed of a top plate (62), a bottom plate (66), and a reactor core (64) disposed between the top an bottom plates. The reactor core has a reaction surface (64a) and a combustion surface (64b), each surface having a raised periphery defining opposing ends (61a and 61b) and opposing sides (63a and 63b). The reaction surface (64a) and the top plate (62) together define a reaction chamber and the combustion surface (64b) and the bottom plate (66) together define a combustion chamber. The reaction core (64) has a first set of a plurality of spaced apart, substantially straight radiating fins (76a) extending from the reaction surface (64a) and a second set of a plurality of spaced part, substantially straight radiating fins (76b) extending from the combustion surface (64b).

Abstract: A method and system for controlling emissions with ammonia recovery and fly ash beneficiation in accordance with the present invention includes introducing ammonia to react with at least a portion of sulfur trioxides in an exhaust emission and result in at least one or more ammoniated compounds. At a least a portion of fly ash particles and the ammoniated compounds in the exhaust emission are precipitated and at least the precipitated fly ash particles are beneficiated. At least a portion of the beneficiated fly ash particles which are heated are mixed with the precipitated ammoniated compounds to recover at least a portion of the ammonia. The recovered ammonia is reused in introducing ammonia to react with at least a portion of sulfur trioxides.

Abstract: The present disclosure provides teachings relating to ammonia-based hydrogen generation apparatus and associated methods of use. Exemplary methods and apparatus comprise a thermocatalytic hydrogen generation reactor which includes a reaction chamber containing a catalyst-coated substrate, and a combustion chamber containing a catalyst-coated substrate. Exemplary catalyst-coated substrates include, but are not limited to, metal foam, monolith, mesh, ceramic foam or ceramic monolith.

Abstract: A virtual analyzer is provided to estimate either an attribute of a reactant applied during performance of, or an amount of a reactant exhausted by, a process having multiple process parameters (MPPs) that is performed to control an amount of a pollutant emitted into the air. The virtual analyzer includes an interface which receives signals corresponding to attributes of the MPPs. If the process is a wet flue gas desulfurization (WFGD) process, the signals include a signal corresponding to a measured pH level of the applied reactant. If the process is a selective catalytic reduction (SCR) process, the signals include a signal corresponding to a measured amount of the reactant exhausted by the process.

Abstract: A method is described for treating a gas stream containing either fuel only or both fuel and oxidant gases, such as hydrogen, nitrous oxide or a hydrocarbon gas. The gas stream is conveyed through a vacuum pumping arrangement comprising a plurality of pumping stages. Either immediately before or immediately after the final pumping stage, the steps of adding a gaseous oxidant to the gas stream and oxidising the fuel gas are performed. By treating the gas stream in this manner, the risk of uncontrolled combustion of the fuel gas can be minimised.

Abstract: Method for the treatment of effluents containing nitrogen in the form of ammonium, according to which: a volume of effluent to be treated in a complete cycle is introduced into the batch reactor in successive volume fractions, each volume fraction being treated during a subcycle: each subcycle comprises a phase of feeding with a volume fraction and, in an alternating manner, two treatment stages, i.e. an aerated first stage, during which complete or partial oxidation of the ammonium so as to give nitrites takes place, followed by a nonaerated second stage, during which the nitrites produced and the ammonium are converted to nitrogen gas. During the aerated first stage, the dissolved oxygen concentration in the batch reactor is maintained between 0.1 mgO2/l and 0.6 mgO2/l; the N—NO2: N—NH4 ratio is adjusted so as to be between 0.9 and 1.5 at the beginning of the nonaerated stage; and the nonaerated phase is carried out by deammonification, without the provision of carbon-based substrate.

Abstract: A technology for purifying an exhaust emission from an engine is provided, in which a misjudgment caused by a time lag between the abnormality detection and an abnormality judgment is avoided, in the case where a plurality of abnormalities is judged on the aqueous solution of a reducing agent or the like. After a first abnormality judgment (Femp=1: the time t2) is made, when a second abnormality is detected as a result that the concentration Dn as a state parameter is directly shifted from a first region A to a second region C (the time t3), the first abnormality judgment is maintained for a predetermined period of time PRD after the second abnormality detection.

Abstract: A solid air filtration medium includes an impregnate with an organic amine and an inorganic metal salt. The medium has from about 0.1 to about 25% by weight of impregnate. The impregnate contains from about 0.1 to about 5% by weight organic amine, and the organic amine includes aqueous urea, solid urea, melamine or mixtures thereof. The impregnate contains from about 0.1 to about 5% by weight metal salt, and the metal salt includes magnesium oxide, calcium oxide or mixtures thereof. The impregnate optionally further includes a surfactant such as polyacrylic acid. Methods for forming a solid air filtration medium having an impregnate containing an organic amine and an inorganic metal salt and methods for removing contaminants from a fluid stream are also provided.

Abstract: By means of a method and a system for heating and partial oxidation of not separately pre-heated, pre-reformed steam/natural gas mixture for an NH3 synthesis gas, whereby energy is supplied to the gas stream (raw synthesis gas), in the direction of flow, after a primary reformer, a solution is to be created, with which soot formation is to be prevented as much as possible, whereby the possibility of the addition of variable amounts, for example of N2 and O2 or mixtures thereof, is also supposed to be possible. This is achieved, according to the method, in that the energy is supplied directly after the primary reformer, by way of at least one pore burner positioned in the gas discharge line of the primary reformer.

Abstract: Combustion flue gas containing NOX and SOX is treated to remove NOX in a multistep system in which NOX is reduced in the flue gas stream via selective catalytic reduction or selective non-catalytic reduction with ammonia or an ammonia-forming compound, followed treatment with hydrogen peroxide to remove residual ammonia and, optionally, treatment with an alkali reagent to reduce residual NOX in the flue gas stream. The NOX-depleted flue gas stream may also be subjected to a desulfurization treatment for removal of SOX.

Abstract: Provided is a process for treating nitrogen oxide-containing exhaust produced by a stationary combustion source by the catalytic reduction of nitrogen oxide in the presence of a reductant comprising hydrogen, followed by ammonia selective catalytic reduction to further reduce the nitrogen oxide level in the exhaust.

Abstract: A method and equipment for removing ammonia from effluent, flue or waste fluids that include oxygen. The method includes at least the following stages: Part of the fluid (1) is conveyed to a decomposition/oxidation unit (2) and part of the fluid (1) is conveyed to a by-pass unit (3); part of the fluid (1) including ammonia is oxidized in the decomposition/oxidation unit (2) of ammonia; the fluid (1H) that was oxidized in the decomposition/oxidation unit (2) and the fluid (1) that was conveyed to the by-pass unit are mixed in a mixing unit (4) to form a fluid mixture (1S), and the fluid mixture (1S) is conveyed to a selective reduction unit (5).

Abstract: Methods and apparatuses are described for contacting an oxidizing solution such as an aqueous hydrogen peroxide composition of hydrogen peroxide and at least one additive that catalyzes the decomposition of the hydrogen peroxide into hydroxyl radicals with an atmospheric effluent containing odorous and/or noxious components. These components are absorbed by the aqueous hydrogen peroxide composition to produce an atmospheric effluent having reduced amounts of the odorous and/or noxious components. Various methods are described for adding the hydrogen peroxide and the decomposition additive.

Abstract: A method for the removal and sequestration of ammonia nitrogen from anaerobic fermentation effluent while producing a higher BTU biogas. The method includes the steps of removing the slurry from the digester, stripping the ammonia from the slurry or portion thereof with a high BTU biogas, blending the stripped ammonia with the digesters biogas to remove the carbon dioxide and precipitate ammonium bicarbonate/carbonate as a solid while producing a high Btu biogas, a portion of which is used to strip the ammonia and CO2 from the slurry. The process removes ammonia nitrogen from the digester effluent while producing a high Btu biogas and a solid ammonium bicarbonate/carbonate product. Ammonia stripping is accomplished with a recycled stripping gas deficient in CO2 and ammonia that is capable of removing the CO2 and ammonia from solution by virtue of the lower partial pressures of CO2 and ammonia in the stripping unit.

Abstract: A process is described that removes by chemical oxidation the excess ammonia (NH3) gas from flue gases that have been subjected to selective catalytic reduction (SCR) and selective non-catalytic reduction (SNCR) of oxides of nitrogen (NOx) by ammonia injection. Methods for the removal of residual ammonia from flue gases prior to fouling air pre-heaters or deposition on fly ash are discussed.

Abstract: A process for the reduction of NOx emissions from a regeneration zone during a fluid catalytic cracking (FCC) process are disclosed. The process comprises contacting a hydrocarbon feedstock with a circulating inventory of an FCC cracking catalyst and a NOx reduction composition during an FCC process. The NOx reduction composition comprises at least one reduced nitrogen species component having the ability to reduce the content of reduced nitrogen species to molecular nitrogen under reducing or partial burn FCC conditions and at least one NOx reduction component having the ability to convert NOx to molecular nitrogen under oxidizing or full burn FCC conditions.

Abstract: The present invention provides a method for binding gaseous molecules, the method comprising contacting gases comprising the gaseous molecules with trivalent metal complexes. Typically, the gaseous molecules comprise polar molecules of greenhouse gases, especially the oxides of carbon, nitrogen and sulphur. Preferably, the trivalent metal complexes comprise complexes of actinide metals, most preferably uranium. The method is particularly useful in the removal of so-called greenhouse gases from the atmosphere, and is therefore of potentially very great value environmentally. The invention also provides trivalent metal complexes comprising sandwich complexes of trivalent metals selected from transition metals and actinide metals, the complexes comprising two ligands selected from pentalenyl, indenyl, cyclopentadienyl and cyclooctatetraene ligands. The invention further provides a method for the preparation of the trivalent metal complexes.

Abstract: A catalyst for nitrogen oxide removal, which catalytically reduces nitrogen oxides in an exhaust gas in the presence of ammonia, comprises: a first component comprising an oxide of titanium, an oxide of tungsten, and an oxide of vanadium; and a second component comprising an oxide of manganese, or an oxide of manganese and an oxide of copper.

Abstract: Improved reactors for catalytic, exothermic gas-phase reactions, which comprise, viewed in the flow direction of a feed gas, an inlet zone (1), a reaction zone (2) containing at least one catalyst (4) an outlet zone (3) for the product gas, are described. The reactors are provided in the region of the inlet zone (1) or in the region of the inlet zone (1) and the reaction zone (2) with means, for example an insulating liner (6) and/or apparatuses for the transport of cooling media, which reduce heat transport from the reaction zone (2) into the inlet zone (1) and thus reduce the risk of preignition of the feed gas mixture used or occurrence of undesirable secondary reactions in the inlet zone (1) and/or the interior walls of the reactor in the region of the inlet zone (1) or in the region of the inlet zone (1) and the reaction zone (2) consist of inert material.

Abstract: A denitrification catalyst and a honeycomb structure type denitrification catalyst which are used for efficiently removing nitrogen oxides through reduction from exhaust gases discharged from, e.g., boilers and internal combustion engines such as a gasoline engine and diesel engine; and a method of denitrification using either of these catalysts. The denitrification catalyst is for use in reducing nitrogen oxides contained in an exhaust gas with an ammonia source and comprises zeolite as the main ingredient, and is characterized in that not only iron element and cerium element but tin element and/or gallium element has been deposited on the zeolite. The honeycomb structure type denitrification catalyst comprises the denitrification catalyst and a honeycomb structure support whose surface has been covered therewith.

Abstract: The present invention is directed to a method for removal by oxidation of the excess ammonia (NH3) gas (“ammonia slip”) resulting from flue gases that have been subjected to selective catalytic reduction (SCR) for reduction of nitrogen oxides (NOx) with ammonia. More specifically, the inventive method uses an ammonia oxidation catalyst consisting of a zeolite, one or more precious metals, and a base metal compound, to catalyze the oxidation of both ammonia and carbon monoxide (CO), while minimizing the formation of nitrogen oxides (NOx). The present invention is useful in treating flue and exhaust gases.

Abstract: Catalysts, methods, and systems for treating diesel engine exhaust streams are described. In one or more embodiments, the catalyst comprises platinum, a second metal from one of the groups VB, VIB, VIIB, VIIIB, IB, or IIB of the periodic table, a refractory metal oxide, and a zeolite, the oxidation catalyst already being effective to remove ammonia at temperatures less than about 300° C. and exhibiting no significant decrease in ammonia oxidation efficiency upon hydrothermal aging. A method aspect includes first passing a vehicle's engine exhaust stream through a NOx abatement catalyst; and passing the exhaust stream exiting the NOx abatement catalyst and containing ammonia through the ammonia oxidation catalyst. Systems including such catalysts are also provided.

Abstract: The invention relates to a process for the chemical beneficiation of raw material containing tantalum-niobium such as wastes, scoria, concentrates and ores.

Abstract: The present invention relates to a catalyst comprising 0.1-10 mol % CO3-xMxO4, where M is Fe or Al and x=0-2, on a cerium oxide support for decomposition of N2O in gases containing NO. The catalyst may also contain 0.01-2 weight % ZrO2. The invention further comprises a method for performing a process comprising formation of N2O. The N2O containing gas is brought in contact with a catalyst comprising 0.1-10 mol % CO3-xMxO4, where M is Fe or Al and x=0-2, on a cerium oxide support, at 250-1000° C. The method may comprise that ammonia is oxidized in presence of an oxidation catalyst and that the thereby formed gas mixture is brought in contact with the catalyst comprising the cobalt component on cerium oxide support at a temperature of 500-1000° C.

Abstract: A method for removing carbon dioxide from a gas stream and controlling ammonia vapor by scrubbing the carbon dioxide from the gas stream with ammonium carbonate, thereby producing ammonia vapor and ammonium bicarbonate; removing a portion of the ammonia vapor from the gas stream with ammonium bicarbonate; and polishing the flue gas to achieve an ammonia concentration of less than 10 PPM.

Abstract: A method of treating fly ash and fly ash treated thereby, the method involving contacting ammonia-laden fly ash with an organic base-containing treatment composition, where the organic base causes the ammonia within the fly ash to evolve from the fly ash. The treatment composition preferably includes an effective amount of one or more amines. The treatment compound may be applied to the fly ash in any manner effective to disperse the treatment compound among the fly ash.

Abstract: The invention relates to a method for removing ammonia and dust from a waste gas that occurs during the production of fertilizers, preferably urea, in which method the waste gas is introduced into a first washer, and a cooling gas is introduced into the one washer and an aqueous solution is introduced into the other washer, whereby both the waste gas and the cooling gas pass through at least one mist collector before exiting from the washer, in each instance, is supposed to be developed further in such a manner that the waste gas pollution can be clearly reduced. This is accomplished in that the additional water is first introduced into a fine-washing area of the first washer, delimited by the mist collector on the top and by a liquid-impermeable partition bottom at the bottom, and sprayed onto the at least one mist collector, and the aqueous solution that forms in the fine-washing area is subsequently passed into the second washer.

Abstract: The present invention provides compositions, systems, and methods for achieving high efficiencies of nitrogen oxide (NOx) removal from exhaust gases while minimizing ammonia slip and sulfur dioxide oxidation. In one embodiment, a method of removing nitrogen oxides from an exhaust gas comprises providing a first catalyst layer, adding an ammonia-containing compound to the exhaust gas upstream of the first catalyst layer in excess of the stoichiometric equivalent of the nitrogen oxides in the exhaust gas, flowing the exhaust gas through the first catalyst layer, selectively catalytically decomposing ammonia in excess of the stoichiometric reaction equivalent of the nitrogen oxides in the exhaust gas, and catalytically reducing the nitrogen oxides by reaction with ammonia not selectively catalytically decomposed.

Abstract: A method for purifying exhaust of waste gas using atomized fluid droplets combined with turbulent flow, including the following steps: a). atomizing the absorption or reacting fluids to microsized droplets; b). enabling waste gas to pass through the aforementioned absorption or reacting fluids and creating a turbulent flow to thoroughly react the waste gas with the droplets; c). reacting of harmful substances in the waste gas with droplets of the absorption or reacting fluids; d). implementing demisting treatment of the waste gas flow; e). discharging the treated waste gas. The aforementioned steps of the present invention enable the purification of waste gas without the need for packing, and achieve high removal efficiency and low energy consumption.

Abstract: Disclosed is a process for the removal of sulfur from a gas stream containing sulfur dioxide, hydrogen cyanide and hydrogen sulfide. The process includes a hydrogenation step, a hydrolysis step, an ammonia removal step and a hydrogen sulfide removal step. An aqueous alkaline washing liquid is used in the hydrogen sulfide removal step and with the spent sulfide containing washing liquid being regenerated using an oxidation bioreactor that utilizes sulfide oxidizing bacteria such as autotropic aerobic cultures of Thiobacillus and Thiomicrospira.

Abstract: This catalyst system simultaneously removes ammonia and enhances net NOx conversion by placing an NH3—SCR catalyst formulation downstream of a lean NOx trap. By doing so, the NH3—SCR catalyst adsorbs the ammonia from the upstream lean NOx trap generated during the rich pulses. The stored ammonia then reacts with the NOx emitted from the upstream lean NOx trap—enhancing the net NOx conversion rate significantly, while depleting the stored ammonia. By combining the lean NOx trap with the NH3—SCR catalyst, the system allows for the reduction or elimination of NH3 and NOx slip, reduction in NOx spikes and thus an improved net NOx conversion during lean and rich operation.

Abstract: The present invention provides an apparatus and method for removing CO gas from gas streams or static air. One application of interest in removing CO from air to provide clean air to breathe or other application such as CO monitoring instruments for calibration, to the air side of the fuel cell and to the reformate stream that is employed for a PEM fuel cell. This invention protects the fuel cell catalyst by a means to controlling CO in the reformate stream. The control system is designed to minimize the CO concentration using the novel CO oxidation catalysts described above. One preferred embodiment catalyzes and monitors the CO to indicate the effectiveness; and further comprising two alternate chambers containing catalyst, which is made of high surface area substrate with supramolecular chemistry coated onto that substrate.

Abstract: A selective catalytic reduction system includes a catalyst, a device to measure an amount of nitrogen oxide (NO), a device to measure an amount of nitrogen dioxide (NO2), a device to add an ammonia source, and a control unit to calculate the amount of ammonia source to add as a function of a ratio of an amount of nitrogen oxide and an amount of nitrogen dioxide or an absolute amount of nitrogen oxide and an absolute amount of nitrogen dioxide.

Abstract: A method for the removal of ammonia and its salts from fluid compositions. The method comprises contacting the fluid compositions with a scavenger on a solid support.

Abstract: A method for treating an ammonia (NH3)-containing gas, which comprises causing the NH3-containing gas to pass through a catalyst tower (9) firstly with a pre-treatment catalyst layer (1) having, in parallel, a flow path involving a catalyst layer having the function of oxidizing NH3 to form NO and a flow path involving a catalyst layer not having the above function, and then, contacting the resultant gas with a catalyst layer (2) having in combination, the denitration function and the function of oxidizing NH3 to form NO; and an apparatus for practicing the method.

Abstract: Processes for selectively removing sulfur-containing compounds from a gas are described herein. The processes generally include contacting a first gas including carbon dioxide and hydrogen sulfide with a scrub solution including ammonium bisulfite and ammonium sulfite in a first contact zone to produce a first contact zone effluent liquid including ammonium thiosulfate and a first contact zone overhead gas in which the concentration of hydrogen sulfide is substantially reduced.

Abstract: Methods and apparatuses are described for contacting an oxidizing solution such as an aqueous hydrogen peroxide composition of hydrogen peroxide and at least one additive that catalyzes the decomposition of the hydrogen peroxide into hydroxyl radicals with an atmospheric effluent containing odorous and/or noxious components. These components are absorbed by the aqueous hydrogen peroxide composition to produce an atmospheric effluent having reduced amounts of the odorous and/or noxious components. Various methods are described for adding the hydrogen peroxide and the decomposition additive.

Abstract: The invention relates to a method for the coproduction of methanol and ammonia from natural gas involving the following steps: 1. Natural gas (flow 1) , steam and oxygen are mixed with one another in a reactor A during which the natural gas is partially oxidized and additionally reformed with the aid of catalysts; 2. The gas mixture removed from reactor A is split into a flow (flow 2) for synthesizing methanol in a unit E and into another flow (flow 3) for producing hydrogen; 3. The carbon monoxide present in flow (flow 3) for producing hydrogen is converted into carbon dioxide inside reactor B with the aid of catalysts and intermediate cooling stages; 4. Remaining impurities such as methane, traces of carbon monoxide and argon are washed out in a cleaning unit D, and hydrogen (flows 6, 8) is fed to the methanol synthesis in unit E and to the ammonia synthesis in unit F; 5.

Abstract: The present invention is directed to a method for removal by oxidation of the excess ammonia (NH3) gas (“ammonia slip”) resulting from flue gases that have been subjected to selective catalytic reduction (SCR) for reduction of nitrogen oxides (NOx) with ammonia. More specifically, the inventive method uses an ammonia oxidation catalyst consisting of a zeolite, one or more precious metals, and a base metal compound, to catalyze the oxidation of both ammonia and carbon monoxide (CO), while minimizing the formation of nitrogen oxides (NOx). The present invention is useful in treating flue and exhaust gases.

Abstract: The disclosure provides methods and systems for sequestering and/or reducing sulfur oxides, nitrogen oxides and/or carbon dioxide present in industrial effluent fluid streams. A solid particulate material comprising a slag component, a binder component (distinct from the slag component), and optionally water is formed and then contacted with the effluent fluid stream to reduce at least one of the sulfur oxides, nitrogen oxides, and/or carbon dioxide. The contacting of the effluent stream may occur in a packed bed reactor with the solid dry particulate material. Methods of reducing pollutants from exhaust generated by combustion sources, lime and/or cement kilns, iron and/or steel furnaces, and the like are provided.

Abstract: Scrubber media for reactive gases, that can include but are not necessarily limited to hydrogen chloride (HCl), hydrogen sulfide (H2S), hydrogen fluoride (HF), and ammonia (NH3), can include reactive particles, potentially as small as nano-scale, that can optionally be suspended on macro-scale carrier particles. Reactive gases can be converted to non-volatile compounds by being passed through a bed of such scrubber media. Such scrubber media can be used to remove reactive gases from gas mixtures. Potential applications include differential absorption spectroscopy, air pollutant emission controls, and the like. Methods of preparing scrubber media are also described.