Gasification is one method for extracting energy from organic materials. Gasification is a process that converts carbonaceous materials, such as coal, petroleum, biofuel or biomass, into carbon monoxide and hydrogen by reacting a raw material at high temperature with a controlled amount of oxygen and/or steam. The resulting gas mixture is called syngas.
One of the byproducts of gasification is ash (e.g., fly ash). Ash is one of the residues generated during the combustion of char in a gasifier. Fly ash includes the fine particles that rise with flue gases. Ash which does not rise is termed bottom ash. Ash material must be removed from the syngas before it can be used as a fuel. Gasification systems typically use one or more separation methods to remove ash from syngas.
Cyclone separators (cyclones) are used to remove particulates from an air, gas or liquid stream, without the use of filters, through vortex separation. Cyclones can be used to remove some of the ash material from the syngas. However, ash particles having particle diameters less than about 10 μm are not easily removed from a gas stream using cyclones. Due to the small particle size of the ash, the ash is not easily separated from the gas stream and much of the ash exits the cyclone with the gas stream. In gasification systems producing ash particles with diameters less than about 10 μm, additional separation steps are needed.
These gasification systems often employ candle filters. Candle filters are often metallic or ceramic, and each has drawbacks. Metallic candle filters are vulnerable to acid gas corrosion. Sulfur and alkali metal oxy-hydroxides within the syngas stream can form acid gas, which corrodes metal candle filters leading to reduced filter life and frequent filter replacement. Ceramic candle filters are fragile and also susceptible to corrosion. Ceramic candle filters are subjected to high temperatures during separation. These high temperatures can lead to cracks in the ceramic candle filter. Constituents of the syngas stream can also corrode or oxidize the ceramics. Both metal and ceramic candle filters are also vulnerable to inter-pore plugging and failure when the ash particles are submicron (diameters less than 1 μm). Additionally, metal and ceramic candle filters are large and expensive to install, operate and maintain.
The slag agglomerator described herein has ceramic matrix composite obstacles (agglomeration cylinders or tubes). The slag agglomerator groups small slag droplets present in the syngas together to facilitate downstream slag removal that does not require candle filters. The small slag droplets impinge on the obstacles, ultimately forming larger slag particles that can be separated from the gas stream using a cyclone.
As noted above, candle filters 108 are susceptible to corrosion, can be fragile, possess a large footprint and require significant installation, operation and maintenance costs. Eliminating candle filters from gasification systems can decrease system cost and increase overall system efficiency. Simply removing candle filters is not an option for gasification systems that produce small particle fly ash, however. The slag agglomerator described herein employs ceramic matrix composite obstacles to increase the particle size of slag (molten fly ash) so that cyclone separation is sufficient to remove fly ash from the gas stream.
At high temperature, fly ash particles melt and form liquid slag droplets. Slag agglomerator 14 increases the particle size of the slag droplets by causing them to agglomerate and grow in size.
Slag agglomerator 14 contains a plurality of obstacles 20 (agglomeration cylinders or tubes) and includes inlet 22 and outlet 24. Obstacles 20 are positioned oblique or perpendicular to the flow of the gas stream. As shown in
Obstacles 20 have exterior surfaces 26 containing a ceramic matrix composite (CMC). As described in further detail below, obstacles 20 are actively cooled to solidify a portion of the slag droplets that impinge on obstacles 20. These frozen slag droplets will stick to the CMC forming a protective coating that prevents detrimental CMC corrosion and erosion. The heat flux through cooled obstacles 20 is maintained so that most of the slag droplets striking obstacles 20 remain molten and either flow down obstacles 20 to be removed from the bottom of slag agglomerator 14 or are re-entrained into the gas flow from the downstream side of obstacles 20 having larger drop sizes. Ceramic matrix composites can tolerate significant tensile stress and thermal shocks without cracking or breaking, making them resistant to the temperatures and forces of the gas stream and slag droplets flowing through slag agglomerator 14. Ceramic matrix composites can provide much more strength than monolithic ceramic materials. Ceramic matrix composites constitute ceramic fibers embedded in a ceramic matrix. The CMC of obstacles 20 includes a matrix component and reinforcing fibers. In one exemplary embodiment, the matrix component of obstacles 20 is silicon carbide (SiC). Silicon carbide has high thermal conductivity properties. Additionally, silicon carbide present on exterior surfaces 26 of obstacles 20 chemically reacts with molten slag droplets. The molten slag droplets react with silicon carbide to form frozen iron silicide (Fe3Si). As slag droplets impinge on exterior surface 26 of obstacle 20, the formed iron silicide produces a bonding layer on exterior surface 26. This bonding layer allows additional slag droplets to solidify and adhere to exterior surface 26 of obstacle 20. The bonding layer eventually covers the upstream side of exterior surface 26, providing additional protection to obstacle 20. In alternative embodiments, the matrix component of obstacles 20 is selected from alumina, silica, chromia, mullite and combinations thereof.
The reinforcing fibers of the CMC used in obstacles 20 provide support to the matrix component. Suitable materials for the reinforcing fibers include carbon, silicon carbide, alumina, mullite and combinations thereof. Silicon carbide fibers include those sold under the trade name Nicalon™ (Nippon Carbon Company). Alumina fibers include those sold under the trade name Nextel 610™ (3M). Mullite fibers include those sold under the trade name Nextel 720™ (3M). Ceramic matrix composites made from the combinations of matrix components and reinforcing fibers described above offer good resistance to thermal shock.
Obstacles 20 are actively cooled so that a portion of the slag droplets that impinges on exterior surfaces 26 of obstacles 20 solidify. As noted above, the gas stream entering slag agglomerator 14 can have a temperature between about 1260° C. (2300° F.) and about 1480° C. (2700° F.). At this temperature, the fly ash present in the gas stream is in a liquid state and forms slag droplets. As a slag droplet impinges on exterior surface 26, heat is transferred from the slag droplet to exterior surface 26, thereby reducing the temperature of the slag droplet. By reducing the temperature of the slag droplet, the droplet transitions from the liquid phase to the solid phase and solidifies on exterior surface 26. Obstacles 20 are cooled to a temperature that causes slag droplets impinging on exterior surface 26 to solidify. In exemplary embodiments, obstacles 20 are cooled so that exterior surfaces 26 have a temperature between about 760° C. (1400° F.) and about 925° C. (1700° F.). This temperature range is below the slag solidus temperature, which is between about 1090° C. (2000° F.) and about 1260° C. (2300° F.). In one embodiment of gasification system 10, obstacles 20 are water cooled. Water used to cool obstacles 20 can be liquid water, steam, superheated steam and combinations thereof. Other coolants such as gaseous nitrogen, argon, carbon dioxide and their combinations can also be used.
As the solid slag coating is formed over obstacles 20, steady-state conditions are reached whereby the heat transferred to the coolant of obstacles 20 is equal to the convective heat transferred to obstacles 20 from the gas stream. At this steady-state condition, no additional freezing of the slag droplets occurs when they impact obstacles 20. Instead, the slag droplets either flow down obstacles 20 to be collected and drained from the bottom of slag agglomerator 14 or the slag droplets are re-entrained into the gas stream from the back-side of obstacles 20 as a droplet with a significantly increased diameter.
In exemplary embodiments, coolant tube 28 is metal, such as stainless steel. A coolant (cooling water, steam, etc.) is delivered from coolant manifold 32 to coolant tube 28 to cool obstacle 20 so that CMC shell 30 and exterior surface 26 is cool enough to cause a fraction of the impinging slag droplets to solidify on exterior surface 26. In exemplary embodiments, the coolant delivered to coolant tubes 28 has a temperature between about 315° C. (600° F.) and about 425° C. (800° F.). The heat absorbed by the coolant in coolant tube 28 can be recovered and used for other purposes (e.g., drive steam turbines, reuse as steam in gasification process).
In exemplary embodiments, coupling 42 is constructed of silicon nitride. This embodiment provides increased thermal efficiency compared to the embodiment illustrated in
However, where a CMC having silicon carbide is used for CMC shell 30, the cooling water must be substantially free of oxygen and have a temperature lower than about 370° C. (700° F.). Oxygen present in the cooling water will react with silicon carbide present in CMC shell 30 to form silica (SiO2). Water will further react with the silica to form silica oxy-hydroxides. These reactions corrode CMC shell 30 and will cause deterioration of obstacle 20. To avoid these reactions, the cooling water used must be substantially free of oxygen. In embodiments where superheated steam is used as the cooling water, the temperature of the superheated steam must be maintained below about 650° C. (1200° F.). Temperatures above this limit can cause the steam to dissociate into molecular hydrogen and molecular oxygen, resulting in the presence of oxygen within the cooling water and subsequent corrosion of obstacle 20.
As slag droplets impinge on exterior surfaces 26 of obstacles 20, some of the slag droplets solidify and adhere to exterior surfaces 26. Additional gas and slag droplets from gasifier 12 are delivered to slag agglomerator 14, resulting in continued slag build up on obstacles 20 until a steady-state coating thickness of solid slag has been reached. Due to the velocity of the gas stream flow through slag agglomerator 14 and the impingement of additional slag droplets, the subsequent molten slag adhered to exterior surfaces 26 of obstacles 20 will eventually flow down exterior surfaces 26 of obstacles 20 or dislodge. The rate of slag dislodge is determined by gas stream velocity, surface tension and slag composition, temperature and viscosity. Typically, the dislodged slag will have a drop size larger than the slag droplets that entered slag agglomerator 14 in the gas stream. This larger drop of dislodged slag will be carried out of slag agglomerator 14 through outlet 24 by the gas stream. Molten slag that flows down exterior surfaces 26 of obstacles 20 to the bottom of slag agglomerator 14 are generally too large to be carried by the gas stream. In one embodiment of slag agglomerator 14, this molten slag will be removed through slag outlet 46 in a bottom portion of slag agglomerator 14 as shown in
Once the gas stream (with slag drops) leaves slag agglomerator 14, the gas stream is quenched at quench station 16. Quench station 16 cools the gas stream using cooling water or other heat exchange material so that syngas and slag particles in the gas stream can be further processed downstream of slag agglomerator 14. The heat absorbed by the cooling water in quench station 16 can be recovered and used for other purposes (e.g., drive steam turbines, reuse as steam in gasification process). Since candle filters are not used in gasification system 10, the gas stream does not need to be cooled as much. In gasification system 100, having candle filters 108, quench station 104 typically needs to cool the gas stream to a temperature below about 370° C. (700° F.). As no candle filters are used in gasification system 10, quench system 16 need only cool the gas stream to a temperature below about 925° C. (1700° F.), increasing the overall efficiency of gasification system 10. The hotter post-quench gas stream in gasification system 10 can also be passed through a heat exchanger to
Cyclone 18 separates the slag particles from syngas in the gas stream. Because the slag droplets impinged on obstacles 20 and exited slag agglomerator 14 as slag having increased particle size, cyclone 18 can sufficiently separate the syngas and slag particles. One or more cyclones 18 can be employed for the separation. Cyclone 18 does not possess the installation, operation or maintenance costs associated with candle filters. Thus, the cost efficiency of gasification system 10 is improved relative to gasification system 100.
A slag agglomerator having ceramic matrix composite agglomeration tubes improves the overall efficiency of a gasification system that produces fly ash particles having small diameters. The slag agglomerator increases the particle size of slag droplets present in syngas to facilitate downstream slag removal that does not require candle filters. Small slag droplets impinge on obstacles within the slag agglomerator to form larger slag particles that can be separated from the gas stream using only a cyclone.
While the invention has been described with reference to an exemplary embodiment(s), it will be understood by those skilled in the art that various changes may be made and equivalents may be substituted for elements thereof without departing from the scope of the invention. In addition, many modifications may be made to adapt a particular situation or material to the teachings of the invention without departing from the essential scope thereof. Therefore, it is intended that the invention not be limited to the particular embodiment(s) disclosed, but that the invention will include all embodiments falling within the scope of the appended claims.
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The International Search Report and Written Opinion of counterpart International Application No. PCT/US2012/046397 filed Jul. 12, 2012. |
Number | Date | Country | |
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20130014439 A1 | Jan 2013 | US |