The present application is a non-provisional application of U.S. Provisional Patent Application No. 62/940,002, filed on Nov. 25, 2019, entitled “Char Preparation System and Gasifier for All-Steam Gasification with Carbon Capture”. The entire contents of U.S. Provisional Patent Application No. 62/940,002 are herein incorporated by reference.
The section headings used herein are for organizational purposes only and should not be construed as limiting the subject matter described in the present application in any way.
Global warming concerns about CO2 greenhouse gas accumulation in the atmosphere continue to grow. Atmospheric concentrations of CO2 are higher now than in any of the last several hundred thousand years. CO2 emissions from fossil fuel energy generation systems are a major culprit in the recent few decades of increasing CO2 in the atmosphere. At the same time, the demand for and use of fossil fuels worldwide continues to grow. Even with major increases in renewables and nuclear energy sources, the growth of fossil fuel consumption continues to rise. As such, there is a significant need for efficient and effective low-carbon technologies, especially for power generation from Hydrogen and/or chemical production.
Integrated gasification combined cycle (IGCC) technology is the cleanest way to make energy from coal. Gasification results in significantly fewer pollutants than produced by conventional coal power plants. An IGCC power plant burns hydrogen rich syngas in a turbine to produce electricity. The excess heat is captured to power a second turbine that produces more electricity, resulting in high-efficiency power generation. Gasification of various solid fuels to produce chemicals including hydrogen, fertilizers, methanol, diesel fuel, and many other chemicals is common today. Gasification is beneficial to the environment, resulting in less pollution, reduced carbon dioxide emission, less solid waste, and lower water use.
The present teaching, in accordance with preferred and exemplary embodiments, together with further advantages thereof, is more particularly described in the following detailed description, taken in conjunction with the accompanying drawings. The skilled person in the art will understand that the drawings, described below, are for illustration purposes only. The drawings are not necessarily to scale, emphasis instead generally being placed upon illustrating principles of the teaching. The drawings are not intended to limit the scope of the Applicant's teaching in any way.
The present teaching will now be described in more detail with reference to exemplary embodiments thereof as shown in the accompanying drawings. While the present teachings are described in conjunction with various embodiments and examples, it is not intended that the present teachings be limited to such embodiments. On the contrary, the present teachings encompass various alternatives, modifications and equivalents, as will be appreciated by those of skill in the art. Those of ordinary skill in the art having access to the teaching herein will recognize additional implementations, modifications, and embodiments, as well as other fields of use, which are within the scope of the present disclosure as described herein.
Reference in the specification to “one embodiment” or “an embodiment” means that a particular feature, structure, or characteristic described in connection with the embodiment is included in at least one embodiment of the teaching. The appearances of the phrase “in one embodiment” in various places in the specification are not necessarily all referring to the same embodiment.
It should be understood that the individual steps of the methods of the present teachings can be performed in any order and/or simultaneously as long as the teaching remains operable. Furthermore, it should be understood that the apparatus and methods of the present teachings can include any number or all of the described embodiments as long as the teaching remains operable.
Global warming and climate change issues are requiring that coal power plants worldwide add expensive controls to capture and store CO2 in order to meet desired emission rates. Current technologies such as IGCC with carbon capture (CC) for coal plants have proven uneconomical without subsidies. The additional power required to run the carbon capture systems reduces efficiency, and consequently widespread adoption has not occurred. This has led to the shutdown of older coal plants and cancellation of many new plants. Still, many experts believe that coal is a valuable energy source to assist in transitioning the world to renewable energy sources.
The present teaching relates to improvements in all-steam gasification system with carbon capture, which can substantially improve both cost and efficiency, and hasten widespread adoption of integrated gasification combined cycle (IGCC) technology. Various aspects of the present teaching relate to the combination and process intensification of matching technologies. Using all-steam gasification (ASG) where the oxygen for gasification and to produce hydrogen comes from steam not an air separation plant combined with an indirect gasifier has numerous advantages because it can supply a source of heat for gasification by the complete combustion of fuel using air. This is accomplished by using an indirect gasifier to keep the products of combustion from mixing with the syngas allowing nitrogen free syngas. This process increases the amount of net hydrogen produced per pound of carbon in the gasifier. Since hydrogen is the carbon-free fuel needed with carbon capture, the increased yield of hydrogen and the use of air instead of oxygen increases IGCC plant efficiency with carbon capture, from about 32% for a conventional system with carbon capture, to about 43% Higher Heating Value (HHV) with the new system. This is greater than 30% more power per pound of coal while capturing more than 90% of the carbon for storage. Due to unique designs in each of the subsystems, there is also an even greater reduction of cost, for both fuel and capital.
A carbonaceous fuel gasification system according to the present teaching includes a micronized char preparation system comprising a devolatilizer that receives solid carbonaceous fuel, hydrogen, oxygen, and fluidizing steam. For example, the solid carbonaceous fuel can be coal, biomass and/or plastic material. The micronized char preparation system produces micronized char, steam, volatiles, and hydrogen at one or more outlets. In some embodiments, the micronized char preparation system includes a counter-flow char cooler that preheats steam as it cools the char, a pressure let-down valve, a pulverizer that reduces the average size of the micronized char to under 10μ, and an airlock that re-pressurizes the micronized char to the inlet.
In some systems, the devolatilizer comprises a heated pressure vessel comprising an inlet for injecting fluidizing steam, and at least one outlet for removing volatiles and coarse char. The char preparation system can include cyclones that separate course char and ash from gases. The cyclones have an outlet that is coupled to an input of an indirect gasifier that is positioned downstream of the devolatilizer. Process intensification that combines multiple functions into a single device has been used to include a micronizing function in this device.
The indirect gasifier includes a vessel comprising a gasification chamber that receives the micronized char from the micronized char preparation system, and that receives a conveying fluid, and steam. The gasification chamber is also sometimes referred to as a gasifier. In this embodiment, the indirect gasifier receives volatiles from the outlet of the micronized char preparation system. In some embodiments, the gasification chamber receives steam from an outlet of the micronized char preparation system. Also, in some embodiments, the gasification chamber (gasifier) has an outlet that is coupled to an inlet of a heat recovery system so that the heat recovery system receives steam from the gasification system. The gasification system produces syngas, ash, and steam at one or more outlets.
The indirect gasifier also includes a combustion chamber. The combustion chamber is sometimes referred to as a combustor. The combustion chamber receives a mixture of hydrogen and oxidant and burns the mixture of hydrogen and oxidant to provide heat for gasification and for heating incoming flows, thereby generating steam and nitrogen. For example, the oxidant can be air. In some embodiments, the oxidant is oxygen or oxygen and CO2 using syngas as the fuel. The heat for gasification is transferred from the combustion chamber to the gasification chamber by circulating refractory sand. In some embodiments, the steam and nitrogen or steam and CO2 generated by the indirect gasifier's combustor are directed to a gas turbine power generation system. In some embodiments, the steam and nitrogen generated by the combustion chamber of the indirect gasifier are directed to an expander connected to an electrical generator, to stack condensers in a power block, and is then exhausted at a system stack.
In various embodiments, the carbonaceous fuel gasification system can further include cyclones that are positioned downstream of the gasifier to separate sand and ash from gases. Also, the carbonaceous fuel gasification system can further include a syngas cooler having an inlet coupled to the outlet of the gasification chamber of the indirect gasifier, where the syngas cooler cools the syngas. In some embodiments, steam can be generated at an outlet. A syngas cleanup system having an input that receives the cooled syngas from the outlet of the syngas cooler can be used to remove impurities. One particular embodiment uses a Warm Gas Clean Up (WGCU) to fit with the capture system
A carbon capture system having an input that is coupled to the outlet of the syngas clean-up system can be used to generate carbon dioxide and hydrogen. Also, in some embodiments, a solid fuel-to-liquids system or other chemical making device is coupled to the outlet of the carbon capture that provides hydrogen.
There are numerous advantages to the carbonaceous fuel gasification system configuration of the present teaching including that the char preparation system eliminates the previous counter-flow char cooler that preheats steam as it cools the char, along with the pressure let-down valve, the pulverizer mill that reduces the average size of the micronized char to under 10μ, and the airlock that re-pressurizes the micronized char to the gasifier inlet pressure. This greatly simplifies and reduces the cost of the system leading to a highly practical commercial system.
In addition, the all-steam gasification system produces a larger quantity of hydrogen per pound of coal or other feedstock compared with other known methods. The use of air and hydrogen for gasification heat eliminates the large expensive air separation plant for producing oxygen, normally used for such systems, significantly improving efficiency and cost. An indirect gasifier enables nitrogen-free hydrogen necessary for polygeneration of liquids and chemicals while maintaining power-only and Coal-to-Liquid (CTL)-only-modes by keeping air from mixing with the critical streams.
Furthermore, the use of micronized char produced in a devolatilizer/char preparation system helps to enable gasification of the feedstock in seconds. This significantly reduces the gasification plant size and provides increased capacity in modularized equipment. A calcium looping system with integral water gas shift, using high temperature fixed beds and limestone-based sorbents enhances the overall carbon capture system and can result in pipeline-quality, high-pressure CO2. Such systems avoid the need for steam to regenerate the sorbents used to capture carbon dioxide. Integrated high temperature heat recovery systems using specialized high temperature heat exchangers support the overall system with very high efficiency. Finally, such systems can utilize known warm-gas clean-up systems that produce near-zero emissions, easing air pollution while reducing temperature cycling.
The embodiment of the all-steam gasification with carbon capture system 100 shown in
One feature of the present teaching is the production of micronized char that advantageously speeds the gasification process and reduces system contamination. The char preparation system 104 prepares micronized char from the coal received from the coal feed system 102 and transfers it to the indirect gasifier 106. To produce micronized char from embodiments of the char preparation system that use coal, the char preparation system 104 receives crushed coal with a size suitable for fluidization. In some embodiments, the fluidization size is less than ¼-inch. Then the crushed coal is micronized in the devolatilizer.
Although it is possible to gasify coal directly without using a char preparation system 104, it is preferable in some systems to first convert the coal into char and then gasify the char. This is because char is much more brittle than coal since most of the interior of the coal particles have been hollowed out by pyrolysis. Pyrolysis produces char particles with a range of geometries. Char particle geometry may comprise a thin-shell sphere. The char particle geometry may also be similar to Swiss cheese in form. The hollowed-out geometry causes char particles to break into far smaller pieces when pulverized than coal. Particles below ten microns are readily achieved. Some particles of pulverized char are ten-times smaller in diameter, and 1000-times smaller in volume, than pulverized coal. The small size of pulverized char particles hastens gasification, which increases viability.
A second feature of using micronized char of the present teaching is that it is non-wetting. Micronized char is non-wetting because the particles remain entrained in the gases in which they flow, rather than colliding with each other or other surfaces. The non-wetting feature avoids the fouling, clinkering, agglomeration, and corrosion common in prior art coal-fired power systems using pulverized coal as the solid fuel.
The indirect gasifier 106 of the present teaching produces syngas from the micronized char. Prior art indirect gasifiers have been used principally to make methane from biomass. As illustrated in
One feature of using the indirect gasifier 107 of the present teaching is that it makes all-steam gasification (ASG) with air possible for applications where nitrogen free syngas is required. Using ASG with air is desirable because indirect gasification eliminates the need for an oxygen plant, also known as an air separation unit (ASU) for fuels production. This is because the products of combustion (POC) are kept separate from the syngas, thereby avoiding the contamination of the syngas by nitrogen in the combustion air. Eliminating the need for an oxygen plant saves a considerable about of cost in construction of the system as reducing the space requirements. Also, indirect gasification creates an improvement in both the efficiency, in the form of a large reduction in auxiliary power required, and the costs of gasification systems used to produce chemicals resulting in considerable ongoing cost savings. An additional important feature of using the indirect gasifier 106 of the present teaching is that the use of hydrogen in the combustion chamber for providing gasification heat by complete combustion allows all the carbon in the coal to be used to produce the maximum amount of hydrogen per pound of coal.
The indirect gasifier 106 receives steam and micronized char from the char preparation system 104. The indirect gasifier combustor 108 receives oxidants and H2. The indirect gasifier also uses volatiles and methane provided by the char preparation system 104. The indirect gasifier combustor 108 produces steam and nitrogen as products of combustion 110. The indirect gasifier produces syngas that is provided to a syngas cooler 112. The syngas cooler 112 cools hot syngas leaving the indirect gasifier 107 to the temperature required by the syngas cleanup system 114.
The syngas cleanup system removes pollutants and sends the syngas to a carbon-capture reactor 116. The carbon capture system 116 uses process intensification to combine multiple function in one fixed bed, pressure swing alternating vessel. These functions can include (1) steam reforming to produce hydrogen from methane; (2) Water Gas Shift (WGS) to produce hydrogen from CO and steam; and (3) Calcium Looping Carbonation (CLC) to capture CO2 and calcining to release CO2. The carbon-capture reactor 116 produces CO2 that is sent to a pipeline. The carbon-capture reactor 116 also produces hydrogen and/or high-hydrogen syngas. Oxygen and, alternatively, spray cooling can be used to adjust temperature in the capture system.
An integrated high temperature heat recovery system 118 provides the steam heating for the gasifier steam and also provides throttle steam for a steam turbine used for power generation. The heat recovery system 118 efficiently recovers the high temperature heat from the water gas shift reaction in the carbon-capture reactor 116. The indirect gasifier 106 can use heat provided by the heat recovery system 118. Also, the carbon-capture reactor 116 can use heat provided by the heat recovery system 118.
It is anticipated that many all-steam gasification with carbon capture systems that use the char preparation system according to the present teaching have the ability to produce chemicals, such as hydrogen and liquid fuels, methanol, ammonia, and urea, in addition to providing power. Hydrogen and/or high hydrogen syngas produced by the carbon-capture reactor 116 can be sent to a coal-to-liquids system 120. For example, the coal-to-liquids system 120 can be a conventional Fischer Tropsch converter.
The coal-to-liquids system 120 can provides an additional adjustment of the hydrogen-to-carbon-monoxide ratio by controlling the bypass around the carbonator in the carbon-capture reactor 116 using a control valve 122.
In some embodiments of the system of the present teaching, the hydrogen from the carbon-capture reactor is also sent to a power block 124. The power block 124 includes a stack condenser for the stack gas that recovers the moisture created by the combustion of the hydrogen. The power block 124 uses steam and N2 from the products of combustion 110. This is important to dilute the hydrogen fuel to reduce flame temperatures to temperatures suitable for modern gas turbines. The stack condensers can provide a system with low water usage compared to conventional IGCCs because the amount of steam required for gasification to produce hydrogen is large and because the power block uses the hydrogen as fuel so there is a large component of water vapor in the gas turbine stack. Condensation is made feasible by the very low sulfur dioxide in the syngas due to the high efficiency of the syngas cleanup system 114. The very low sulfur dioxide content syngas also eliminates the corrosion of the stack that would otherwise occur. The power block 124 typically would include a relatively large sized steam turbine to accommodate the many steam sources other than the gas turbine heat recovery steam generator.
Air extraction from a gas turbine for process air flows is used in many known conventional integrated gasification combined cycle (IGCC). The optimal amount of air extraction depends on economic and operating considerations. Some embodiments of the power block 124 of the present teaching use a different amount of air extraction as compared to known power blocks. This is, at least in part, because hydrogen is used as the principal fuel and the products of combustion system 110 flows of steam and nitrogen are returned to the gas turbine in the power block 124. As such, the optimum amount of air extraction is different from any known IGCC air extraction systems. Embodiments of the power block 124 used for various polygeneration applications such as heating, cooling and electricity production, will also use a different optimum amount of air extraction than most known IGCC.
The all-steam gasification with carbon capture system 100 of
An all-steam gasification system for polygeneration with carbon capture according to the present teaching includes a devolatilizer that pyrolyzes solid fuel to produce char and gases that includes a burner that adds exothermic heat to gasses by high-pressure sub-stoichiometric combustion to reduce or eliminate oxidation of char in the devolatilizer, a mixing pot that causes turbulent flow of hot gases provided by the burner to heat received solid fuel, and a riser that micronizes resulting friable char. A devolatilizer cyclone separates the micronized char by weight providing sufficiently micronized char, steam and pyrolysis gases to a gasifier feed and providing oversized micronized char a recycling input of the mixing pot. An all-steam indirect fluid bed gasifier combustion loop includes a gasifier coupled to devolatilizer gasifier feed, an input for receiving steam to provide oxygen for gasification reactions and to facilitate sand-char separation, and an output that provides syngas. A burner provides POC to a mixing pot which provides hot sand with POC to a POC cyclone via a riser, where the POC cyclone separates hot sand and POC by weight and provides POC and sand for a steam-carbon reaction.
In one embodiment according to the present teaching, the devolatilizer is configured to have a mixing pot 302 at its bottom and then a high-velocity riser 304 on top of the mix pot which operates in the turbulent fluidized-bed mode. The rapid heating of the coal in the mix pot/riser causes the coal to swell up rapidly and become friable. The high velocity in the riser micronizes the friable char into particles that are in the 10- to 20-μm range as the high velocity solids impact on the corner at the top of the riser and on the wall of the devolatilizer cyclone. Solids that are not fine enough to escape the cyclone are recycled back into the bottom of the mix pot/riser. In various embodiments a single or a multi-stage cyclone such as a two-stage cyclone are used.
Exothermic heat is added to the process via the high-pressure sub stoichiometric combustion of recycled syngas or hydrogen and oxygen in a separate standalone burner. Steam is also injected into this separate stand-alone burner to superheat the combustion. As a result, none of the circulating char is oxidized in the mixing pot 302. The inlet gas temperature is typically limited to ˜2000° F. to prevent bed agglomeration due to localized hot spots.
The configuration shown in
The solids circulation into the mixing zone is controlled by fluffing gas in the standpipe, L-valve 306 aeration flows, and solids level in the standpipe 308. In some embodiments, the L-valve 306 is a non-mechanical solid flow device which controls the solids flow rate around the gasifier/combustor loop. The quantity and quality of pulverized char and pyrolysis gas leaving the devolatilizer 300 is a function of the operating velocity, solids circulation rate, gas density, and operating temperature of the system. The micronized char, micronized ash, and devolatilized gases are then transferred into the bottom of a fluidized, bubbling-bed gasifier.
It is often desirable to keep the total facility height low. This can be achieved in part by using a refractory lined pipe to transfer the devolatilizer char and pyrolysis gases to the bottom of the ASG gasifier, which will be located at a similar height adjacent to the devolatilizer 300.
Crushed coal or another solid fuel is first fed into a mixing pot 302. Hydrogen and oxygen are input and burned using a combustor at the bottom of the reactor. The solids circulation into the mixing zone is controlled by fluffing gas in the standpipe, J-leg aeration flows, and solids level in the standpipe. The quantity and quality of pulverized char and pyrolysis gas leaving the devolatilizer will be a function of the operating velocity, solids circulation rate, gas density, and operating temperature of the system. The micronized char, micronized ash, and devolatilized gases are then transferred through one or more cyclones into the bottom of a fluidized, bubbling-bed gasifier. The overhead bed also thermally cracks the tars in the volatiles, rendering them into gaseous hydrocarbons such as methane. Steam is used to fluidize the bed. Oxygen is used instead of air in the devolatilizer to avoid the contamination of the volatiles by the nitrogen from the air. This allows the nitrogen-free syngas to be used for polygeneration or to produce coal-to-liquids.
In some methods according to the present teaching, a devolatilizer additive is injected into the devolatilizer in order to neutralize the effect of sodium-based contaminants. The devolatilizer additive prevents and reduces undesirable deposits that are common in known integrated gasification combined cycle (IGCC) coolers and candle filters.
The combustor loop section 404 of the indirect gasifier 400 is used to generate the required heat for the reaction. The circulating fluid bed uses the combusting of hydrogen-rich syngas with air to heat sand in the mixing pot 402 at the bottom of the fluid bed's riser section 406. Alternatively, for various oxy-fired applications, syngas can be combusted with an oxygen-carbon dioxide mixture. The circulating fluid bed is connected with a low-velocity bubbling fluid-bed ASG, which can be heated by the hot solids returning from the circulating fluid bed. For example, sand having dimensions that are approximately 350-μm can be used. However, one skilled in the art will appreciate other material and/or other dimensions of materials can be used. For many methods, a substantial sand or other material recirculation rate is required to supply enough heat required for gasification.
One feature of the apparatus of the present teaching is that the interconnected side-by-side fluid-bed configuration described herein can be more efficient at keeping the syngas and the products of syngas combustion flue gas stream separated. Furthermore, this configuration can also results in reasonable solid flux rates, less solid entrainment into the syngas, and more flexibility in vessel heights and diameters while simultaneously allowing for better separation of micronized char from the gasifier solids flowing to the combustor mix pot. These features are desirable in that they minimize the oxidation of char into the flue gas.
In operation, the heated sand and products of combustion (POC) gases are separated by the POC cyclone 408. The moving bed of hot sand from the bottom of the POC cyclone 408 provides the gas seal between the gasifier 410 and the combustor loop sections 404. The heated sand in the circulating fluid bed is in fluid communication with the low-velocity bubbling fluid-bed, which is the actual gasification portion of the ASG indirect gasifier 400. The sand is transferred to the gasifier 410 from the POC cyclone 408 via a dipleg and an automatic L-valve 409. The hot sand provides the required heat for the steam-carbon reaction in the gasifier section 410. The bubbling bed gasifier section provides turbulent solids intermingling of the hot sand and the micronized char, which promotes gasification of the char. The turbulent flow in the bubbling bed also supports separation of more dense sand particles from char and residue ash. Sand with minimal char entrainment settles to the bottom of the bubbling bed and ultimately moves into the downcomer of the combustion section of the combustor 404. Furthermore, sand-char separation is facilitated by injecting steam into the gasifier above the entrance to the downcomer. The sand-filler downcomer provides a gas seal between the combustor 404 and gasifier 410 sections of the ASG indirect gasifier 400. The moving bed of sand is transferred into the bottom of the mixing pot 402 for reheating via the L-valve 409.
Sand attrits as it loops within the ASG indirect gasifier 400. In the gasifier section, the high operating pressure and high viscosities of the gas produce a substantial drag on the particles. This strong drag force can cause some smaller sand particles to be carried out of the gasifier in the syngas exit stream along with fine, micronized ash and residual carbon. The sand particles are large and heavy and should be removed from this stream before the syngas stream enters the heat recovery heat exchangers and solids filter. The gasifier can also have a cyclone in some embodiments. The POC cyclone 408 positioned in the syngas exit stream remove the larger, heavier sand particles. The sand is then recirculated back into the gasifier section via the L-valve 409.
The syngas stream leaving the ASG indirect gasifier 400 will contain some unconverted carbon. In some embodiments, a second ASG system is employed to provide a second stage of gasification to attain near complete carbon conversion.
While the Applicant's teaching is described in conjunction with various embodiments, it is not intended that the Applicant's teaching be limited to such embodiments. On the contrary, the Applicant's teaching encompass various alternatives, modifications, and equivalents, as will be appreciated by those of skill in the art, which may be made therein without departing from the spirit and scope of the teaching.
Number | Name | Date | Kind |
---|---|---|---|
2582711 | Nelson | Jan 1952 | A |
2689787 | Ogorzaly et al. | Sep 1954 | A |
2772954 | Jequier | Dec 1956 | A |
3373562 | Wormser | Mar 1968 | A |
3988237 | Davis et al. | Oct 1976 | A |
4002438 | Fleming | Jan 1977 | A |
4003691 | Wormser | Jan 1977 | A |
4013395 | Wormser | Mar 1977 | A |
4051791 | Wormser | Oct 1977 | A |
4135885 | Wormser | Jan 1979 | A |
4149559 | Wormser | Apr 1979 | A |
4253409 | Wormser | Mar 1981 | A |
4279205 | Perkins et al. | Jul 1981 | A |
4279207 | Wormser | Jul 1981 | A |
4303023 | Perkins et al. | Dec 1981 | A |
4400181 | Snell et al. | Aug 1983 | A |
4499857 | Wormser | Feb 1985 | A |
4578175 | Gorin | Mar 1986 | A |
4823712 | Wormser | Apr 1989 | A |
5122346 | Wormser | Jun 1992 | A |
5236354 | Goldbach et al. | Aug 1993 | A |
5469698 | Garcia-Mallol | Nov 1995 | A |
5536488 | Mansour et al. | Jul 1996 | A |
5655853 | Wormser | Aug 1997 | A |
5688296 | Andrus et al. | Nov 1997 | A |
5728361 | Holley | Mar 1998 | A |
5917136 | Gaffney et al. | Jun 1999 | A |
5997220 | Wormser | Dec 1999 | A |
6863820 | Cabrera et al. | Mar 2005 | B2 |
6877322 | Fan | Apr 2005 | B2 |
7314847 | Siriwardane | Jan 2008 | B1 |
7951350 | Taylor | May 2011 | B1 |
8110523 | Ryu et al. | Feb 2012 | B2 |
9174844 | Ramkumar et al. | Nov 2015 | B2 |
9873840 | Wormser | Jan 2018 | B2 |
10443005 | Wormser et al. | Oct 2019 | B2 |
10570348 | Wormser et al. | Feb 2020 | B2 |
20020117564 | Hahn et al. | Aug 2002 | A1 |
20040045272 | Miyoshi et al. | Mar 2004 | A1 |
20040123601 | Fan | Jul 2004 | A1 |
20040237404 | Andrus et al. | Dec 2004 | A1 |
20060000143 | Suichi et al. | Jan 2006 | A1 |
20060207177 | Andrus et al. | Sep 2006 | A1 |
20060260189 | Reddy et al. | Nov 2006 | A1 |
20070256359 | Wiltowski | Nov 2007 | A1 |
20080021251 | Laccino et al. | Jan 2008 | A1 |
20080119356 | Ryu | May 2008 | A1 |
20090217585 | Raman et al. | Sep 2009 | A1 |
20100050654 | Chiu et al. | Mar 2010 | A1 |
20100181539 | Apanel et al. | Jul 2010 | A1 |
20100281878 | Wormser | Nov 2010 | A1 |
20100329963 | Sceats et al. | Dec 2010 | A1 |
20120000175 | Wormser | Jan 2012 | A1 |
20120164032 | Wormser | Jun 2012 | A1 |
20120167585 | Wormser | Jul 2012 | A1 |
20120247080 | Ishii et al. | Oct 2012 | A1 |
20120267577 | Sceats et al. | Oct 2012 | A1 |
20130239479 | Gao | Sep 2013 | A1 |
20140044632 | Zielinski et al. | Feb 2014 | A1 |
20140158939 | Ramkumar et al. | Jun 2014 | A1 |
20140296586 | Chandran et al. | Oct 2014 | A1 |
20140314629 | Lee | Oct 2014 | A1 |
20140352581 | Abanades Garcia et al. | Dec 2014 | A1 |
20150013575 | Yazdanpanah et al. | Jan 2015 | A1 |
20170003732 | Wendel et al. | Jan 2017 | A1 |
20170037328 | Wormser | Feb 2017 | A1 |
20170096335 | Wormser | Apr 2017 | A1 |
20180073430 | Forrest et al. | Mar 2018 | A1 |
20200002631 | Wormser | Jan 2020 | A1 |
20200148963 | Wormser | May 2020 | A1 |
20210347638 | Wormser et al. | Nov 2021 | A1 |
20220073828 | Todd et al. | Mar 2022 | A1 |
Number | Date | Country |
---|---|---|
2740315 | Apr 2010 | CA |
1272870 | Nov 2000 | CN |
1407948 | Apr 2003 | CN |
1642620 | Jul 2005 | CN |
1676210 | Oct 2005 | CN |
1795257 | Jun 2006 | CN |
1903431 | Jan 2007 | CN |
101235321 | Aug 2008 | CN |
101269320 | Sep 2008 | CN |
101378826 | Mar 2009 | CN |
101443275 | May 2009 | CN |
102549119 | Jul 2012 | CN |
102575178 | Jul 2012 | CN |
102665871 | Sep 2012 | CN |
203096004 | Jul 2013 | CN |
114729275 | Jul 2022 | CN |
0 067 580 | Dec 1982 | EP |
0 227 550 | Jul 1987 | EP |
0274637 | Jul 1988 | EP |
0619455 | Oct 1994 | EP |
2457636 | May 2012 | EP |
2484971 | Aug 2012 | EP |
2006-300476 | Nov 2006 | JP |
245651 | Apr 1995 | TW |
280849 | Jul 1996 | TW |
442572 | Jun 2001 | TW |
I237103 | Aug 2005 | TW |
0250214 | Jun 2002 | WO |
2006044317 | Apr 2006 | WO |
2007045048 | Apr 2007 | WO |
2007123776 | Nov 2007 | WO |
2008157433 | Dec 2008 | WO |
2009039393 | Mar 2009 | WO |
2010045232 | Apr 2010 | WO |
2011035241 | Mar 2011 | WO |
2011047409 | Apr 2011 | WO |
2013062800 | May 2013 | WO |
2013-109616 | Jul 2013 | WO |
2021108395 | Jun 2021 | WO |
Entry |
---|
Mark Sceats, The Endex Configuaration for CaO Looping Reactors, Sep. 2009, Calix Ltd. |
K. Fouhi, Coal Comes Back, Chemical Engineering, Aug. 1, 1991, pp. 47-48ccc, vol. 98, No. 8, Access Intelligence Association, Rockville, MA, US. |
Andrus, et al., Alstom's Calcium Oxide Chemical Looping Combustion Coal Power Technology Development, May 31-Jun. 4, 2009, 12 pages, the 34th International Technical Conference on Clean Coal & Fuel System, Clearwater, Florida. |
Rietveld, et al., Commercialization of the ECN Milena Gasification Technology, Jun. 2014, 21 pages. |
Twin IHI Gasifier (TIGAR®), Current Status of Indonesia Demostration Project and its Business Plan, Oct. 18, 2016, 19 pages, IHI Corporation, Vancouver, Canada. |
Butler, Limestone as a Sorbent for CO2 Capture and its Application in Enhanced Biomass Gasification, Oct. 2013, 279 pages, The University of British Columbia, Vancouver, Canada. |
Fan, Preparation of Calcium Oxide-Based absorbent and its CO2 absorption Performance, China Excellent Master's Thesis Full-text Database, Engineering Technology Series I, May 15, 2017, No. 05, pp. B016-241. |
Ahn, et al. Review of Supercritical CO2 Power Cycle Technology and Current Status of Research and Development, Nucl Eng Technol, 2015, pp. 647-661, vol. 47, Elsevier. |
“Notification of Transmittal of the International Search Report and the Written Opinion of the International Searching Authority, or the Declaration” for International Patent Application No. PCT/US2020/061994, dated Mar. 16, 2021, 10 pages, ISA/KR, Korean Intellectual Property Office, Daejeon, Republic of Korea. |
“International Preliminary Report on Patentability” received for PCT Application Serial No. PCT/US2020/061994 dated Jun. 9, 2022, 07 pages. |
Carpenter et al., “Pilot-Scale Gasification of Corn Stover, Switchgrass, Wheat Straw, and Wood: 1. Parametric Study and Comparison with Literature”, Ind. Eng. Chem. Res., vol. 49, No. 4, 2010, pp. 1859-1871. |
Number | Date | Country | |
---|---|---|---|
20210155860 A1 | May 2021 | US |
Number | Date | Country | |
---|---|---|---|
62940002 | Nov 2019 | US |