1. Field of the Disclosure
The disclosure relates to a process for operating a coal-fired utility boiler. The disclosure further relates to a burner useful in a coal-fired utility boiler. The disclosure further relates to a coal-fired utility boiler having a burner therein.
2. Description of the Related Art
Utility boilers or furnaces are employed in industry for generation of heat, production of steam, and generation of electricity utilizing steam. Utility boilers typically have a furnace therein where a fuel is oxidized or burned to generate heat. Along with generating heat, utility boilers will generate or evolve an exhaust gas and/or flue gas that will contain carbon dioxide, residual oxygen (unreacted), inert air components, i.e., nitrogen and argon, and emissions, such as sulfur-based and nitrogen-based compounds. Exhaust gas and/or flue gas is typically treated and then vented to the atmosphere.
A variety of problems are encountered when operating utility boilers. Such problems generally relate to slag deposition, fouling, cleanliness, efficiency, and emissions.
Emissions problems relate to sulfur-based emissions, such as sulfur dioxide (SO2), sulfur trioxide (SO3), and sulfuric acid (H2SO4); nitrogen-based emissions (NOx), such as nitrous oxide (NO) and nitrogen dioxide (NO2); mercury-based emissions (Hg) and particulates. Free sulfur trioxide in an exhaust gas and/or a flue gas imparts an undesirable opaque appearance (a blue haze or trailing plume) to the gas when vented to the atmosphere. Free sulfuric acid can cause corrosion of process surfaces in utility boilers as well as acid rain in the atmosphere. Particulate emissions are made up of unburned carbon and ash. Unburned carbon is formed when burning of oil in a boiler is incomplete. Particulates have to be captured and/or vented the atmosphere. Particulates also absorb and transport free acid. Ash is naturally present in coal. Particulates also present cleanliness and industrial hygiene problems.
Slag deposition can take the form of one or more layers caked/baked onto process surfaces. The one or more layers typically contain silica, aluminum, calcium, and metal complexes of vanadium with sodium, nickel, iron, or magnesium. Slag can deposit on the surfaces of tube bundles or other heat transfer devices within the utility boiler denuding a boiler's heat transfer efficiency.
Chemical additives have been employed in the art in utility boilers to reduce or minimize slag deposition, fouling, cleanliness, efficiency, and emissions in utility boilers and exhaust gas or flue gas. Such additives have been added directly to utility boilers and/or to fuel intended for such boilers.
Addition of chemical additives to coal-fired utility additives has proven problematic. Additives are frequently used in a liquid form for ease of use and precise metering of amounts added. When liquid-based additives are sprayed onto feed coal, the additives are usually absorbed or adsorbed into the feed coal. When the treated feed coal reaches the boiler, the additive may volatilize prior to the combustion of the char or matrix of the coal. Thus, the additive is substantially unavailable to assist in or to otherwise be present during oxidation or burning of the coal. Direct introduction of additives into coal-fired boilers has likewise heretofore been ineffective due to non-homogeneous or ineffectual distribution of additives within the boiler. The potential benefits of the additives have been compromised or denuded by such non-homogeneous or ineffectual distribution and/or have required excess make-up amounts of additives.
It would be desirable to have a process for operating a coal-fired utility boiler in which additives can be effectively introduced such that slag deposition, fouling, cleanliness, and undesirable emissions can be reduced or minimized. It would also be desirable to have a process for operating a coal-fired utility boiler that affords enhanced operational efficiency.
According to the present disclosure, there is a process for operating a coal-fired utility boiler. The process has the steps of (a) providing coal and one or more additives in proximity to one or more burners in the boiler; (b) providing air to the boiler; and (c) burning the coal and the one or more additives in the boiler to generate heat and an exhaust gas. Useful functionalities for the one or more additives include (i) reduction in slag formation, (ii) generation of oxygen, (iii) reduction in acid formation, (iv) reduced fouling, (v) reduction in sulfur compound formation, (vi) reduction in nitrogen compound formation, (vii) reduction in particulate formation, and (viii) capture of heavy metals.
Further according to the present disclosure, there is a burner. The burner has a first conduit for transporting a fuel; a second conduit for transporting air; a third conduit for transporting an additive; and an igniter adapted to initiate combustion of the fuel and the air. The first conduit, the second conduit, and the third conduit are longitudinally coextensive with each other. The third conduit is positioned within the first conduit and the second conduit. Either the first conduit or the second conduit is positioned within the other. The burner is adapted to maintain a continuous flame after initiation of combustion.
Further according to the present disclosure, there is a coal-fired utility boiler. The boiler has a furnace chamber adapted to combust coal and air and one or more burners positioned within the chamber. The one or more burners each include a first conduit for transporting the coal, a second conduit for transporting air, a third conduit for transporting an additive, and an igniter adapted to initiate combustion of the fuel and the air. The first conduit, the second conduit, and the third conduit direct the coal, the air, and the additive proximal to the igniter. The one or more burners each are adapted to maintain a continuous flame after initiation of combustion.
In the present disclosure, additives are introduced into the boiler in proximity to the burner(s), i.e., in proximity to the flame(s) (jet(s)) thereof to reduce slag deposition, fouling, amount of undesirable emissions, and enhance cleanliness. Introduction of additives in proximity to the burner substantially prevents premature volatilization of the additives (compared to pretreatment of coal) and allows the additives to be present and/or burned substantially concurrently with the char or matrix of the coal. Further, introduction of additives in proximity to the burner substantially mitigates the effects of non-homogeneous or ineffectual distribution of additives within the boiler as the additives are readily available for burning and/or chemical treatment or modification of the coal or its combustion products and byproducts as the coal is burned. The mitigation of the effects of the non-homogeneous or ineffectual distribution of additives also reduces or eliminates the amount of make-up additives required.
Preferably, the additives are introduced directly to the flame(s) produced by the burner(s). More preferably, additives are injected directly into or on the flame(s) by means of lances. In a preferred embodiment, additives are injected in liquid form through a hollow lance or probe within a lance. The lance or probe preferably has an atomizer at its distal end to effect spraying into or on the flame(s).
The additives are most preferably injected into the internal recirculation zone (IRZ) of the flame. The IRZ typically extends about 0.5 diameters to about 4 diameters downstream and preferably about 0.5 diameters to about 2 diameters downstream of the burner. The term “diameters” correlates to the diameter of the burner throat. Injection of additives into the IRZ functions to stabilize the flame and promote complete combustion of the coal. An IRZ can be formed by burner aerodynamic hardware, e.g., a swirler, and impeller, and a flame stabilizer. The location of an IRZ relative to an embodiment of a burner is depicted by way of illustration in
An embodiment of the process of the present disclosure is set forth in
An embodiment of a burner is generally referenced by the numeral 40 and is shown in cross-section in
Another embodiment of a burner is generally referenced by the numeral 140 and is shown in perspective in
Various additives are employed in the present disclosure for controlling slag formation, fouling, emissions levels, and the like. Additives useful in controlling such process variables include metal compounds of lithium, magnesium, calcium, selenium, manganese, iron, cerium, copper, platinum, aluminum, and zirconium. Useful compounds include the following: oxides, carbonates, carboxylates, salicylates, naphthenates, and sulfonates, hydroxides, salicylates, nitrates, borates, and bromides.
Slag control agents can be employed in the process of the present disclosure to prevent buildup of slag deposits within the furnace of the utility boiler and other process surfaces during the combustion of coal. Conversion of undesirable vanadium compounds, such as vanadium pentoxide and sodium vanadium pentoxide, to more innocuous vanadium compounds helps to prevent or reduce catalysis of sulfur dioxide to sulfur trioxide, corrosion of process surfaces due to acid exposure, and deposition of vanadium compounds on process surfaces inside the utility boiler.
Useful slag control agents include, but are not limited to, the following: magnesium hydroxide; magnesium oxide; magnesium carbonate; and magnesium organometallic compounds, such as magnesium carboxylate, magnesium salicylate, magnesium naphthenate, and magnesium sulfonate. Preferred slag control agents are magnesium hydroxide, magnesium oxide, and organometallic magnesium carboxylate with magnesium carbonate overlay.
Oxygen-generating agents can be employed in the process of the present disclosure to provide additional oxygen at the situs of oxidation or burning in the furnace, which allows the percent of excess air, i.e., excess oxygen, supplied to the utility boiler to be reduced and/or minimized. Lower excess air content reduces the amount of SO3 and NOx formed. Use of the oxygen-generating agent also reduces the incidence of unburned carbon, i.e., reduces incidence of particulate formation, due to more efficient combustion or burning. Use of the oxygen-generating agent also reduces the amount of coal required to produce a given amount of energy hence enhancing power generation efficiency and economy and lowering per capita emission levels. Reduction of unburned carbon also reduces the incidence and retention of sulfuric acid, which is absorbed by unburned carbon.
Useful oxygen-generating agents include, but are not limited to, the following: calcium nitrate, calcium organometallic compounds, calcium salicylate, calcium sulfonate, overbased calcium carboxylate, iron oxides, iron carboxylates, iron organometallic compounds, iron sulfonates, barium oxide, barium carbonate, barium carboxylate, barium organometallic compounds, and barium sulfonate. Preferred oxygen-generating agents are the calcium compounds. Most preferred oxygen-generating agents are calcium nitrate and calcium carboxylate.
Acid mitigation agents can be employed in the process of the present disclosure to reduce or minimize the amount of acidic compounds in the boiler and the exhaust gas and/or flue gas. Particularly, the agent reacts with sulfuric acid to form innocuous, non-acidic compounds thereby reducing acid emissions in the exhaust gas and/or flue gas and corrosion of process surfaces within the boiler. Acid mitigation agents can either neutralize or absorb/adsorb acids. Examples of acid mitigation agents include magnesium oxide, magnesium hydroxide, magnesium carbonate, sodium bicarbonate carbonate, and calcium carbonate.
Fouling prevention agents can be employed in the process of the present disclosure to reduce or minimize buildup on process surfaces within the boiler and maintain operational efficiency. Examples of fouling prevention agents include magnesium oxide, magnesium hydroxide, magnesium carbonate, and sodium borate.
Oxidizer agents can be employed in the process of the present disclosure to (i) reduce or minimize excessive air addition to the furnace and (ii) help convert mercury and heavy metal constituents to an oxidized form that is easier to capture. Examples of oxidizer agents include calcium bromide, calcium chloride, and sodium bromide.
Heavy metal capture agents can be employed in the process of the present disclosure to reduce or minimize mercury emissions. A preferred heavy metal capture agent is a mercury capture agent. Examples of mercury capture agents include calcium sulfide, calcium polysulfide, and sodium sulfide. Heavy metal capture agents are preferably incorporated outside the boiler into one of its auxiliary devices. For example, the agent can be injected into the exhaust system or added to a flue gas desulfurization unit. The agent can take the form of a dry or wet system.
The additives can be used in any known product form, such as a mineral ore, a powder, or liquid. Liquids may be water-based, oil-based, or a combination thereof. Liquids may take any known liquid form, such as solutions, slurries, suspensions, dispersions, or emulsions. Liquid forms are preferred since they can be injected or sprayed with precision via conventional pumping and metering devices. A preferred means of adding additives into the burner is via injection in liquid form in proximity to a burner.
The amount of slag control agent employed can vary depending upon a variety of process and composition conditions. Typically conditions include type of slag control agent selected, load or feed rate of the fuel, amount and type of oxygen-generating agent used, amount or feed rate of air, and impurity composition of the fuel. When a liquid form of the slag control agent is used, the amount employed will typically vary from about 1:2000 to about 1:6000 agent:agent, volume:volume.
The amount of slag control agent or other additives employed in coal can be expressed in terms of parts per million (ppm) and weight percent. The amount of slag control agent(s) employed can also be expressed in terms of “times stoichiometry” in reference to a certain emission, such as SO3. Dosage typically ranges from about 100 ppm to about 5 weight percent based on the weight of the coal and may vary depending on the type of additive.
The amount of oxygen-generating agent employed can vary depending upon process and composition conditions. Conditions include type of oxygen-generating agent selected, load or feed rate of coal, amount and type of slag control agent used, amount or feed rate of air, and impurity composition of the coal. When a liquid form of the oxygen-generating agent is used, the amount employed will typically vary from about 1:1000 to about 1:10000 and preferably about 1:2500 to about 1:4000 agent:coal, volume:volume. Expressed as a function of weight, the amount of slag control agent(s) employed typically varies from about 25 ppm to about 3 weight percent.
In the present disclosure, additives are introduced to a boiler system in proximity to the burners. It is possible, however, to add other additives (of the same or different composition) to other areas of the boiler or to an auxiliary device thereof. An auxiliary device is an inlet or outlet apparatus or component of a boiler outside of the furnace or direct heating section thereof. For instance, heavy metal capture agents, such as mercury capturing agents, are sometimes added at an exhaust system and/or a flue gas desulfurization unit as an alternative to, or in addition to, introduction into a furnace or direct heating section thereof.
Coal useful in the process of the present disclosure can be of any form known in the art, such as anthracite, bituminous, sub-bituminous, lignite, pet coke, and charcoal. Coal is preferably pulverized prior to introduction into the boiler.
The burner(s) can be fueled by any known useful burner fuel, such as a flammable gas or fuel oil. Useful flammable gases include natural gas, propane, and butane.
Conventional process components and equipment may be utilized to control and vary the feed rates of the coal and/or additives. Examples of useful process components and equipment include, but are not limited to, flow limiting/controlling devices such as valves; pumps; fans; and conveyor belts.
The process of the present disclosure is preferably carried out substantially continuously.
Additional teachings regarding the use of additives in coal-fired utility boilers are found in U.S. Ser. No. 12/319,994, filed Jan. 14, 2009, which is incorporated herein by reference in their entireties.
U.S. Provisional Patent Application No. 61/349,452, filed May 28, 2010, entitled “A Process for Operating a Coal-fired Utility Boiler”, is incorporated herein by reference.
It should be understood that the foregoing description is only illustrative of the present disclosure. Various alternatives and modifications can be devised by those skilled in the art without departing from the disclosure. Accordingly, the present disclosure is intended to embrace all such alternatives, modifications and variances that fall within the scope of the appended claims.
The present application claims priority based on U.S. Provisional Application No. 61/425,894, filed Dec. 22, 2010, and U.S. Provisional Application No. 61/349,452, filed May 28, 2010, both of which are incorporated herein by reference in their entireties.
Number | Date | Country | |
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61425894 | Dec 2010 | US | |
61349452 | May 2010 | US |