The present invention relates to a method for ultra-low NOx combustion of fuels, even high hydrogen and low BTU content gases, including, without limitation, syngas, gasified coal, and natural gas. The present invention provides a method for separately supplying fuel and air to a reactor for in-situ mixing and reaction prior to combustion with additional air.
With energy usage directly related to economic growth, there has been a steady increase in the need for increased energy supplies. In the U.S., coal is abundant and comparatively low in cost. Unfortunately, conventional coal-fired steam power plants, which are a major source of electrical power, are inefficient and pollute the air. Thus, there is a pressing need for cleaner, more efficient coal-fired power plants. Accordingly, Integrated Gasification Combined Cycle (“IGCC”) coal technology systems have been developed which can achieve significantly improved efficiencies in comparison to conventional steam plants. In such a system, syngas (a mixture of hydrogen and carbon monoxide) is produced by partial oxidation of coal or other carbonaceous fuel. This allows cleanup of sulfur and other impurities, including mercury, before combustion.
Concern over global warming resulting from carbon dioxide emissions from human activity, primarily the combustion of fossil fuels, has led to the need to sequester carbon. If carbon dioxide sequestration is desired, the carbon monoxide can be reacted with steam using the water gas shift reaction to form carbon dioxide and hydrogen. Carbon dioxide may then be recovered using conventional technologies known in the art. This allows pre-combustion recovery of carbon dioxide for sequestration. Removal of the carbon dioxide leaves a fuel gas much richer in hydrogen. Unfortunately, there is an issue for low NOx combustion for these high hydrogen fuels.
As a result of the high flame speed of hydrogen, flashback is likely with premixed dry low NOx combustion systems. Flashback remains an issue with the use of syngas as well. Regardless of whether carbon dioxide is recovered or whether air or oxygen are used for syngas production, hydrogen content of the gas typically is too high to allow use of conventional dry low NOx premixed combustion for NOx control. Therefore, diffusion flame combustion is used typically with steam or nitrogen added as a diluent to the syngas from oxygen blown gasifiers to minimize NOx emissions. Even so, exhaust gas cleaning may still be required. Thus, such systems, though cleaner and more efficient, typically cannot achieve present standards for NOx emissions without NOx clean-up methods.
A further problem is that the presence of diluent in the fuel increases mass flow through the turbine often requiring the bleeding off of compressor discharge air to reduce turbine rotor stresses. Since bleed off of compressor air must be limited to allow sufficient air for combustion and turbine cooling, the amount of diluent which can be added to the fuel is limited. Typically, NOx cannot be reduced below about ten parts per million (“ppm”) without operational problems, including limited flame stability. There are further efficiency loss issues. If nitrogen is added to dilute the fuel gas, there is an energy penalty related to the need to compress the nitrogen to the pressure required for mixing with the fuel gas. In addition, use of syngas in a gas turbine designed for natural gas increases turbine mass flow even without dilution for NOx reduction. Typically, to avoid excessive loads on the turbine rotor, operation is at a reduced turbine inlet temperature and/or with bleed of compressed air from the turbine compressor. Low BTU gases also have a high content of diluents and may require rotor protection.
It has previously been shown that rich pre-combustion with transfer of reaction heat allows low NOx formation in diffusion flame combustion; for example, as taught in U.S. Publication No. 2007/0037105 (U.S. patent application Ser. No. 11/439,727). Using a reactor such as that described in U.S. Pat. No. 6,394,791, the content of which is incorporated herein, the stoichiometric flame front temperature (“SFFT”) of high hydrogen content fuels can be reduced sufficiently to provide ultra-low NOx combustion. Unfortunately, some high hydrogen fuels are difficult to safely premix.
It has now been found that with a backside cooled reactor, the need for fuel-air premixing can be eliminated for fuels by direct injection of both fuel and air into the catalytic reactor flow channels with in-situ mixing of the fuel and air. As discussed in this invention, fuels include any known fuels such as, for example, natural gas, low BTU content gas, syngas (including coal derived and carbon reduced syngas), hydrogen and the like. Whether or not conditions may provide ignition of the fuel upon contact with air, the reactor is substantially protected having backside cooled walls. Moreover, the fuel flow can be used to inject much more air than would otherwise flow through the available effective open area, thus allowing greater fuel conversion in the reactor and thus greater reduction in the stoichiometric flame front temperature (“SFFT”) on contact with the cooling air. By reducing SFFT, NOx is reduced. With a fuel flow air injector, air flow increases with increased fuel flow and decreases with decreased fuel flow, yielding lower part load reactor flame temperatures and thus lower catalyst temperatures. With hydrogen fuels, conditions can readily be chosen to provide reaction of the hydrogen upon contact with the injected air. In this case, no catalyst is needed on the tubes.
As indicated by CFD (Computational Fluid Dynamics) analysis, mixing is very rapid. Experimental in-situ mixing has demonstrated good stability and performance.
As shown in
Although the mixing in the figure occurs in parallel jet stream, other methods typical for premixing such as perpendicular jet penetration, etc. are part of the present invention. In addition, as stated in the Summary of the Invention, with hydrogen fuels, conditions can readily be chosen for use with hydrogen fuels to provide reaction of the hydrogen upon contact with the injected air such that no catalyst is needed on the tubes.
Upon contact between the fuel and air, ignition may occur inside the catalytic channels. Since all surfaces are actively cooled, the reactor is not damaged. For instance, all the catalyst coated elements are cooled internally via cooling air path (2). The fuel distribution plate (4) is backside cooled by the incoming fuel in the chamber of fuel distribution plenum (5). The reactor housing (not shown) has a high thermal mass and may be cooled from an external air flow. This can be provided by having the air flow to the reactor pass over the housing before introduction to the reactor or a separate air stream could provide cooling.
Further, if gas phase combustion does occur within the catalytic channels, it is advantageous due to high conversion of catalytic air from catalytic air path (1) and increase in the transfer of the heat of combustion to the cooling air flow of cooling air path (2). This may lead to lower downstream NOx emissions. Whether or not gas phase ignition occurs, conversion of fuel is promoted by reaction on the catalytic cooling tube walls.
An important aspect of the present invention is that the adiabatic stoichiometric flame temperature of high hydrogen content fuels can be reduced sufficiently to allow ultra low NOx diffusion flame combustion, even for the highest inlet temperature gas turbines thus allowing wide turndown. As shown in
While the present invention has been described in considerable detail, other configurations exhibiting the characteristics taught herein for direct injection for low NOx combustion of fuels including natural gas as well as high hydrogen fuels are contemplated. For example, other catalytic reactor designs are contemplated as well as non-catalytic gas phase combustion. A portion of the fuel may also be injected upstream into air so as long as the stoichiometric condition of the resultant fuel/air mixture is below the autoignition limit. Therefore, the spirit and scope of the invention should not be limited to the description of the preferred embodiments described herein.
This invention was made with government support under U.S. Contract No. DE-FC26-05NT42647. The U.S. government holds certain rights in this invention
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