An apparatus is provided that receives waste and generates electrical power or thermal energy with minimal NOx emissions. A gasifier is provided that receives the waste and air to produce fuel gas for delivery to a fluidly coupled reformer. The reformer receives the fuel gas, recycled flue gas, and air to auto-thermally produce a reformed fuel gas and destroy fuel gas pollutants at a first temperature without a catalyst. A burner is fluidly coupled to the reformer and receives recycled flue gas and air to oxidize the reformed fuel gas at a second temperature that prevents nitrogen oxide formation, the second temperature being lower than the first temperature. A quench chamber is fluidly coupled to the burner and receives flue gas from the burner for quenching with recycled flue gas. A heat recovery system is fluidly coupled to the reformer, burner, and quench chamber to extract usable energy.

An apparatus is provided that receives waste and generates electrical power or thermal energy with minimal NOx emissions. A gasifier is provided that receives the waste and air to produce fuel gas for delivery to a fluidly coupled reformer. The reformer receives the fuel gas, recycled flue gas, and air to auto-thermally produce a reformed fuel gas and destroy fuel gas pollutants at a first temperature without a catalyst. A burner is fluidly coupled to the reformer and receives recycled flue gas and air to oxidize the reformed fuel gas at a second temperature that prevents nitrogen oxide formation, the second temperature being lower than the first temperature. A quench chamber is fluidly coupled to the burner and receives flue gas from the burner for quenching with recycled flue gas. A heat recovery system is fluidly coupled to the reformer, burner, and quench chamber to extract usable energy.

A gas clean-up unit includes a first conversion unit configured to perform a first conversion process of converting hydrogen cyanide contained in gas to be treated to ammonia, in presence of a first catalyst and at a first predetermined temperature; a second conversion unit configured to perform a second conversion process of converting carbonyl sulfide in the gas that has been subjected to the first conversion process to hydrogen sulfide, in presence of a second catalyst and at a second predetermined temperature lower than the first predetermined temperature; a cleaning unit configured to perform a cleaning process of bringing the gas into gas-liquid contact with cleaning liquid to remove the ammonia by cleaning; and a desulfurization unit configured to absorb and remove hydrogen sulfide in the gas by bringing the gas that has been subjected to the cleaning process into gas-liquid contact with absorbent.

A catalytically active filter for use in hot gas filtration to simultaneously remove solid particles and one or more undesirable compounds from a hot gas stream is partly or fully impregnated with a suitable catalyst. The compounds are selected from HCN, arsenic, organic sulfur compounds and carbonyls. The filter is prepared by making an impregnation liquid, which comprises a catalytically effective amount of at least one active metal and an oxide support, impregnating the filter substrate with the impregnation liquid by dipping it in the liquid or spraying it with the liquid to control the amount of liquid and drying and optionally calcining the impregnated filter.

A catalyst for selectively oxidizing hydrogen sulfide to element sulfur, catalyst for burning tail-gas, and process for deeply catalytically oxidizing hydrogen sulfide to sulfur are disclosed. The catalyst for selectively oxidizing hydrogen sulfide to element sulfur is prepared by: 10-34% of iron trioxide and 60-84% of anatase titanium dioxide, and the balance being are auxiliary agents. Also a catalyst for burning tail-gas is prepared by: 48-78% of iron trioxide and 18-48% of anatase titanium dioxide, and the balance being auxiliary agents. The catalyst of the present invention has high selectivity and high sulfur recovery rate. An isothermal reactor and an adiabatic reactor of the present invention are connected in series and are filled with the above two catalysts for reactions, thus reducing total sulfur in the vented gas while having a high sulfur yield and conversion rate.

A catalyst for selectively oxidizing hydrogen sulfide to element sulfur, catalyst for burning tail-gas, and process for deeply catalytically oxidizing hydrogen sulfide to sulfur are disclosed. The catalyst for selectively oxidizing hydrogen sulfide to element sulfur is prepared by: 10-34% of iron trioxide and 60-84% of anatase titanium dioxide, and the balance being are auxiliary agents. Also a catalyst for burning tail-gas is prepared by: 48-78% of iron trioxide and 18-48% of anatase titanium dioxide, and the balance being auxiliary agents. The catalyst of the present invention has high selectivity and high sulfur recovery rate. An isothermal reactor and an adiabatic reactor of the present invention are connected in series and are filled with the above two catalysts for reactions, thus reducing total sulfur in the vented gas while having a high sulfur yield and conversion rate.

Catalysts for oxidative sulfur removal and methods of making and using thereof are described herein. The catalysts contain one or more reactive metal salts dispersed on one or more substrates. Suitable reactive metal salts include those salts containing multivariable metals having variable valence or oxidation states and having catalytic activity with sulfur compounds present in gaseous fuel streams. In some embodiments, the catalyst contains one or more compounds that function as an oxygen sponge under the reaction conditions for oxidative sulfur removal. The catalysts can be used to oxidatively remove sulfur-containing compounds from fuel streams, particularly gaseous fuel streams having high sulfur content. Due to the reduced catalyst cost, anticipated long catalyst life and reduced adsorbent consumption, the catalysts described herein are expected to provide a 20-60% reduction in annual desulfurization cost for biogas with sulfur contents ranges from 1000-5000 ppmv compared with the best adsorbent approach.

Catalysts for oxidative sulfur removal and methods of making and using thereof are described herein. The catalysts contain one or more reactive metal salts dispersed on one or more substrates. Suitable reactive metal salts include those salts containing multivariable metals having variable valence or oxidation states and having catalytic activity with sulfur compounds present in gaseous fuel streams. In some embodiments, the catalyst contains one or more compounds that function as an oxygen sponge under the reaction conditions for oxidative sulfur removal. The catalysts can be used to oxidatively remove sulfur-containing compounds from fuel streams, particularly gaseous fuel streams having high sulfur content. Due to the reduced catalyst cost, anticipated long catalyst life and reduced adsorbent consumption, the catalysts described herein are expected to provide a 20-60% reduction in annual desulfurization cost for biogas with sulfur contents ranges from 1000-5000 ppmv compared with the best adsorbent approach.

A device and method for cleaning producer gas includes a filter bed housing and a microwave chamber. The filter bed housing comprises an inlet for carbon-based material and a spent carbon outlet. The microwave chamber comprises a permeable top and wave guides around the perimeter through which microwaves can be introduced into the device using magnetrons. The method comprises using the device by filling the filter bed housing with carbon-based material, introducing microwaves into the microwave chamber using the magnetrons and wave guides, passing the gas through carbon-based material in the filter bed chamber, the microwave chamber, the gas permeable top and the gas outlet.

A device and method for cleaning producer gas includes a filter bed housing and a microwave chamber. The filter bed housing comprises an inlet for carbon-based material and a spent carbon outlet. The microwave chamber comprises a permeable top and wave guides around the perimeter through which microwaves can be introduced into the device using magnetrons. The method comprises using the device by filling the filter bed housing with carbon-based material, introducing microwaves into the microwave chamber using the magnetrons and wave guides, passing the gas through carbon-based material in the filter bed chamber, the microwave chamber, the gas permeable top and the gas outlet.