The proposed invention relates to a system and method for removing carbon dioxide (CO2) from a process gas stream containing carbon dioxide and sulphur dioxide. More particularly, the proposed invention is directed to a system and method for removing CO2 gas from a flue gas stream by contacting a flue gas stream to a CO2 absorbent that is disposed upon a solid material.
Embodiments of the present invention provide a system and method for capturing carbon dioxide (CO2) from a process gas stream. Briefly described, in architecture, one embodiment of the system, among others, can be implemented so as to include an absorber vessel configured to receive a flue gas stream via a flue gas inlet.
Embodiments of the present invention can also be viewed as providing a method for removing CO2 from a flue gas stream. In this regard, one embodiment of such a method, among others, can be broadly summarized by the following steps: exposing a flue gas to an absorbent; and exposing the absorbent to a regeneration gas stream.
Other systems, methods, features, and advantages of the present invention will be or become apparent to those with ordinary skill in the art upon examination of the following drawings and detailed description. It is intended that all such additional systems, methods, features, and advantages be included within this description, be within the scope of the present invention, and be protected by the accompanying claims.
In the combustion of a fuel, such as coal, oil, natural gas, peat, waste, etc., in a combustion plant, such as those associated with boiler systems for providing steam to a power plant, a hot process gas (or flue gas) is generated. Such a flue gas will often contain, among other things, carbon dioxide (CO2) The negative environmental effects of releasing carbon dioxide to the atmosphere have been widely recognised, and have resulted in the development of processes adapted for removing carbon dioxide from the hot process gas generated in the combustion of the above mentioned fuels. Systems and methods have been proposed for removing CO2 from a gas stream. These systems and methods include CO2 capture systems in which a flue gas is contacted with an aqueous absorbent solution such as, for example, a chilled ammonia based ionic solution such as that described and claimed in pending patent application PCT/US2005/012794 (International Publication Number: WO 2006/022885/Inventor: Eli Gal)), filed on 12 Apr. 2005 and titled Ultra Cleaning of Combustion Gas Including the Removal of CO2.
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The ionic solution is put into contact with the flue gas stream via a gas-liquid contacting device (hereinafter, mass transfer device, MTD) 111 used for mass transfer and located in the absorber vessel 170 and within the path that the flue gas stream travels from its entrance via inlet 76 to the vessel exit 77. The gas-liquid contacting device 111 may be, for example, one or more commonly known structured or random packing materials, or a combination thereof.
Ionic solution sprayed from the spray head system 121 and/or 122 falls downward and onto/into the mass transfer device 111. The ionic solution cascades through the mass transfer device 111 and comes in contact with the flue gas stream FG that is rising upward (opposite the direction of the ionic solution) and through the mass transfer device 111.
Once contacted with the flue gas stream, the ionic solution acts to absorb CO2 from the flue gas stream, thus making the ionic solution “rich” with CO2 (rich solution). The rich ionic solution continues to flow downward through the mass transfer device and is then collected in the bottom 78 of the absorber vessel 170. The rich ionic solution is then regenerated via regenerator system 74 (see
After the ionic solution is sprayed into the absorber vessel 170 via spray head system 122, it cascades downward onto and through the mass transfer device 111 where it is contacted with the flue gas stream FG. Upon contact with the flue gas stream the ionic solution reacts with CO2 that may be contained in the flue gas stream. This reaction is exothermic and as such results in the generation of heat in the absorber vessel 170. This heat can cause some of the ammonia contained in the ionic solution to change into a gas. The gaseous ammonia then, instead of migrating downward along with the liquid ionic solution, migrates upward through the absorber vessel 170, along with and as a part of the flue gas stream and, ultimately, escaping via the exit 77 of the absorber vessel 170.
These known CO2 capture systems require substantial equipment, such as pumps and storage tanks, to transport, cool/heat, circulate/recirculate and store ionic solution.
Further, features of the present invention will be apparent from the description and the claims.
Many aspects of the invention can be better understood with reference to the following drawings. The components in the drawings are not necessarily to scale, emphasis instead being placed upon clearly illustrating the principles of the present invention. Moreover, in the drawings, like reference numerals designate corresponding parts throughout the several views. The invention will now be described in more detail with reference to the appended drawings in which:
The proposed invention is directed to capturing CO2 gas from a flue gas stream by subjecting the flue gas stream to an absorbent that is coated on to a solid material or substrate, generally referred to herein as an absorbent coated substrate (ACS) 300.
The flue gas input 221 and the exhaust outlet 223 are each provided, respectively, with a damper (260 & 262, respectively) that is controlled to be either “open” or “closed”, depending up the processing stage (“absorption stage” or “regeneration stage”) that the ACS absorber system 250 is engaged in.
The ACS absorber 275 is further provided with a regeneration gas inlet 222 and a CO2 outlet 224. The regeneration gas input and the CO2 outlet are each provided, respectively, with a damper (261 & 263, respectively) that is controlled to be either “open” or “closed”, depending up the processing stage (“absorption stage” or “regeneration stage”) that the ACS absorber system 250 is engaged in.
In a preferred embodiment the ACS 300 includes an absorbent that is coated (or otherwise applied) onto a substrate. The absorbent may be, for example, an amine or amine compound. Some examples, of amines and/or amine compounds that may be utilized as an absorbent, include, but are not limited to aqueous monoethanolamine (MEA), diglycolamine (DGA), diethanolamine (DEA), diisopropanolamine (DIPA) and/or methyldiethanolamine (MDEA), hydrogen sulfide (H2S) tetraethylenepentamine (TEPA), an acrylonitrile-modified tetraethylenepentamine (TEPAN), triethylenetetramine (TETA), and/or an acrylonitrile-modified ethyleneamine (ME-100), or other chemical. In a preferred embodiment, the absorbent is an acrylonitrile-modified tetraethylenepentamine (TEPAN).
The substrate may be composed of, for example, polymethyl methacrylate (PMMA) spheres such as those commonly available from suppliers such as, for example Dow Chemicals, Inc., Huntsman, BASF, and others. The substrate may also be composed of high surface area structure or material.
The ACS 300 is placed into an ACS absorber vessel 275 as generally depicted in
After a period of time, the absorbent of the ACS 300 will become saturated with CO2 that has been captured from a flue gas stream that contains CO2. Once the absorbent becomes saturated, it's ability to capture further CO2 from the flue gas stream is greatly reduced, if not completely lost. At this point, the absorbent of the ACS 300 can be refreshed or “regenerated” to make it capable of further CO2 capture.
In a preferred embodiment, the absorbent is refreshed during the regeneration stage of system operation. During the “regeneration stage” the ACS 300 in the ACS absorber vessel 275 is exposed to regeneration gas received into the ACS absorber via the hot regeneration gas input. This is generally depicted in
The ACS absorber vessel 275 is configured to receive regeneration gas that may be pulled from, for example, an additional adjacent/nested ACS absorber vessel (see
In a further embodiment, the ACS may be regenerated by evacuating CO2 from the ACS absorber 275 by reducing the pressure at the discharge side of the vessel 275 (via, for example, applying a vacuum to the vessel 275). The CO2 could then be collected for further processing/treatment. In this embodiment, the vessel 275 may be configured to allow a hot regeneration gas to be pulled into the vessel 275 as the pressure within the vessel 275 is reduced.
In a preferred embodiment, the ACS absorber system will include a controller 290 for controlling, among other things, the dampers 260, 261, 262 and 263 and fans (280) in the system based upon predetermined criteria and input from one or more sensors (not shown) that provide input signals/data to indicate a then current status of various system features, attributes and equipment. The controller 290 is configured to issue commands or signal outputs to the dampers and/or fans, as may be appropriate, to control or otherwise adjust such things as gas flow, gas flow paths, temperature and atmosphere within the system.
The flue gas stream migrates upward and through one of more beds of ACS 300 that are disposed within the interior of the absorber vessel 275. As the flue gas passes through the ACS 300, it is contacted with the ACS 300 whereby CO2 contained in the flue gas stream is captured by the absorbent of the ACS 300.
The use of a solid material, such as PMMA (Polymethyl methacrylate) spheres for CO2 absorption and desorption will reduce, if not totally eliminate, the need to pump amine or other absorbent solutions from tanks into absorber vessels and then to regenerators to remove CO2 from gas streams. This will eliminate the need for pumps, tanks and other expensive hardware, as well as costs associated with operating such.
The proposed invention can minimize the need for pumping of liquid streams for CO2 removal and recovery from gas streams. Further, the proposed invention allows for costs savings due to the reduced need for pumping, heating and/or cooling equipment, as well as the costs associated with reduced energy usage/consumption.
Additionally, a reduction in thermal energy requirements for the regeneration step can be achieved. The low temperature requirements for each process (absorption and regenerations) allows the proposed invention to provide an economical alternative to conventional capture systems and processes. Similarly, since the system is dry it is not necessary to heat all the liquid phases to drive reactions thus resulting in significant energy savings.
It should be emphasized that the above-described embodiments of the present invention, particularly, any “preferred” embodiments, are merely possible examples of implementations, merely set forth for a clear understanding of the principles of the invention. Many variations and modifications may be made to the above-described embodiment(s) of the invention without departing substantially from the spirit and principles of the invention. All such modifications and variations are intended to be included herein within the scope of this disclosure and the present invention and protected by the following claims.
This application claims priority to copending U.S. provisional application entitled, “CO2 Absorption by Solid Materials”, having U.S. Ser. No. 61/012,799 filed on Dec. 11, 2007, the disclosure of which is entirely incorporated herein by reference.
Number | Date | Country | |
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61012799 | Dec 2007 | US |