US 8,083,836 B2Grant
Method and apparatus for extracting carbon dioxide from air
Issue Date:2011-12-27
•14 Claims
•16 Drawing Sheets
Abstract
A method and apparatus for extracting CO2 from air comprising an anion exchange material formed in a matrix exposed to a flow of the air, and for delivering that extracted CO2 to controlled environments. The present invention contemplates the extraction of CO2 from air using conventional extraction methods or by using one of the extraction methods disclosed; e.g., humidity swing or electro dialysis. The present invention also provides delivery of the CO2 to greenhouses where increased levels of CO2 will improve conditions for growth. Alternatively, the CO2 is fed to an algae culture.
Metadata
Assignee
- Kilimanjaro Energy, Inc.
Inventors
- Allen B. Wright
- Klaus S. Lackner
- Ursula Ginster
Application Information
Application Number:US 12/903,967
Filing Date:2010-10-13
Priority Date:2006-10-02
Art Unit:1776
Classifications
IPC:
B01D53/02
Patent Drawings (16 sheets)
Description
Cross Reference to Related Applications
[0001] The present application is a continuation of U.S. patent application Ser. No. 12/638,717, filed Dec. 15, 2009, which in turn is a divisional of 11/866,326, filed Oct. 2, 2007, now U.S. Pat. No. 7,708,806, claims priority from U.S. Provisional Application Ser. No. 60/827,849, filed Oct. 2, 2006, and 60/829,376, filed Oct. 13, 2006, the contents of which are incorporated herein by reference.
Field of the Invention
[0002] The present invention in one aspect relates to removal of selected gases from air. The invention has particular utility for the extraction and sequestration of carbon dioxide (CO2) from air and will be described in connection with such utilities, although other utilities are contemplated.
Background of the Invention
[0003] There is compelling evidence to suggest that there is a strong correlation between the sharply increasing levels of atmospheric CO2 with a commensurate increase in global surface temperatures. This effect is commonly known as Global Warming. Of the various sources of the CO2 emissions, there are a vast number of small, widely distributed emitters that are impractical to mitigate at the source. Additionally, large scale emitters such as hydrocarbon-fueled power plants are not fully protected from exhausting CO2 into the atmosphere. Combined, these major sources, as well as others, have lead to the creation of a sharply increasing rate of atmospheric CO2 concentration. Until all emitters are corrected at their source, other technologies are required to capture the increasing, albeit relatively low, background levels of atmospheric CO2. Efforts are underway to augment existing emissions reducing technologies as well as the development of new and novel techniques for the direct capture of ambient CO2. These efforts require methodologies to manage the resulting concentrated waste streams of CO2 in such a manner as to prevent its reintroduction to the atmosphere.
[0004] The production of CO2 occurs in a variety of industrial applications such as the generation of electricity power plants from coal and in the use of hydrocarbons that are typically the main components of fuels that are combusted in combustion devices, such as engines. Exhaust gas discharged from such combustion devices contains CO2 gas, which at present is simply released to the atmosphere. However, as greenhouse gas concerns mount, CO2 emissions from all sources will have to be curtailed. For mobile sources the best option is likely to be the collection of CO2 directly from the air rather than from the mobile combustion device in a car or an airplane. The advantage of removing CO2 from air is that it eliminates the need for storing CO2 on the mobile device.
[0005] Extracting carbon dioxide (CO2) from ambient air would make it possible to use carbon-based fuels and deal with the associated greenhouse gas emissions after the fact. Since CO2 is neither poisonous nor harmful in parts per million quantities, but creates environmental problems simply by accumulating in the atmosphere, it is possible to remove CO2 from air in order to compensate for equally sized emissions elsewhere and at different times.
[0006] Most prior art methods, however, result in the inefficient capture of CO2 from air because these processes heat or cool the air, or change the pressure of the air by substantial amounts. As a result, the net loss in CO2 is negligible as the cleaning process may introduce CO2 into the atmosphere as a byproduct of the generation of electricity used to power the process.
[0007] Various methods and apparatus have been developed for removing CO2 from air. For example, we have recently disclosed methods for efficiently extracting carbon dioxide (CO2) from ambient air using capture solvents that either physically or chemically bind and remove CO2 from the air. A class of practical CO2 capture sorbents include strongly alkaline hydroxide solutions such as, for example, sodium or potassium hydroxide, or a carbonate solution such as, for example, sodium or potassium carbonate brine. See for example published PCT Application PCT/US05/29979 and PCT/US06/029238.
[0008] There are also many uses for sequestered CO2. This includes the use of CO2 in greenhouses where higher levels of CO2 contribute to increased plant growth. CO2 may also be supplied to algae cultures. Researchers have shown that algae can remove up to 90% of gaseous CO2 from air streams enriched in CO2 and can also reduce the CO2 concentration in ambient air.
Summary of the Invention
[0009] The present invention provides a system, i.e. a method and apparatus for extracting carbon dioxide (CO2) from ambient air and for delivering that extracted CO2 to controlled environments.
[0010] In a first exemplary embodiment, the present invention extracts CO2 from ambient air and delivers the extracted CO2 to a greenhouse. Preferably, the CO2 is extracted from ambient air using a strong base ion exchange resin that has a strong humidity function, that is to say, an ion exchange resin having the ability to take up CO2 as humidity is decreased, and give up CO2 as humidity is increased. Several aspects of this invention can also be used to transfer CO2 from the collector medium into the air space of a greenhouse where the CO2 is again fixed in biomass. In a preferred embodiment of the invention, CO2 is extracted from ambient air using an extractor located adjacent to a greenhouse, and the extracted CO2 is delivered directly to the interior of the greenhouse for enriching the greenhouse air with CO2 in order to promote plant growth.
[0011] In a second exemplary embodiment, this invention allows the transfer of CO2 from a collector medium into an algae culture, where the CO2 carbon is fixed in biomass. The algae biomass can then be used for the production of biochemical compounds, fertilizer, soil conditioner, health food, and biofuels to name just a few applications or end-uses.
[0012] This invention also discloses transfer of CO2 in gaseous phase and as a bicarbonate ion. In one embodiment, a calcareous algae is used which creates calcium carbonate CaCO3 internally, and precipitates the CaCO3 out as limestone.
[0013] Accordingly, in broad concept, the present invention extracts CO2 from ambient air using one of several CO2 extraction techniques as described, for example, in our aforesaid PCT/US05/29979 and PCT/US06/029238. Where a carbonate/bicarbonate solution is employed as the primary CO2 sorbent, the CO2 bearing sorbent may be used directly as a feed to the algae. Where the CO2 is extracted using an ion exchange resin as taught, for example in our aforesaid PCT/US06/029238 application, the CO2 is stripped from the resin using a secondary carbonate/bicarbonate wash which then is employed as a feed to the algae. In a preferred alternative embodiment, the carbonate is fed to the algae in a light enhanced bioreactor.
[0014] Thus, the present invention provides a simple, relative low-cost solution that addresses both CO2 capture from ambient air and subsequent disposal of the captured CO2.
Brief Description of the Drawings
[0015] Further features and advantages of the present invention will be seen from the following detailed description, taken in conjunction with the accompanying drawings, wherein
[0016] FIG. 1 is a block flow diagram illustrating the use of humidity sensitive ion exchange resins in accordance with the present invention;
[0017] FIGS. 2 a and 2b are schematic views of a CO2 extractor/greenhouse feeder in accordance with the present invention, where filter units are located adjacent an exterior wall;
[0018] FIGS. 3 a and 3b are schematic views of a CO2 extractor/greenhouse feeder in accordance with the present invention, where filter units are located adjacent to the roof of the greenhouse;
[0019] FIG. 4 is a schematic view of a CO2 extractor/greenhouse feeder showing an arrangement of filter units according the present invention;
[0020] FIG. 5 is a schematic view of a CO2 extractor/greenhouse feeder showing filter units arranged on a track according to an alternative embodiment of the present invention;
[0021] FIG. 6 is a schematic view of a CO2 extractor/greenhouse feeder including convection towers according to an alternative embodiment of the present invention;
[0022] FIG. 7 is a schematic view of a CO2 extractor and algae culture according to the present invention utilizing a humidity swing applied to a collector medium;
[0023] FIG. 8 is a schematic view of a CO2 extractor and algae culture according to the present invention utilizing a humidity swing applied to a collector solution;
[0024] FIG. 9 is a schematic view of a CO2 extractor and algae culture according to the present invention transferring gaseous CO2 by an electro-dialysis process;
[0025] FIG. 10 is a schematic view of a CO2 extractor and algae culture according to the present invention transferring bicarbonate by an electro-dialysis process;
[0026] FIG. 11 is a schematic view of a CO2 extractor and algae culture according to the present invention utilizing an algae culture for collector regeneration;
[0027] FIG. 12 is a schematic view of a CO2 extractor and algae culture similar to FIG. 11 utilizing a nutrient solution;
[0028] FIG. 13 is a schematic view of a CO2 extractor and algae culture according to the present invention utilizing a gas-permeable membrane;
[0029] FIG. 14 is a schematic view of a CO2 extractor and algae culture according to the present invention utilizing an anion-permeable membrane;
[0030] FIG. 15 is a schematic view of a CO2 extractor and algae culture similar to FIG. 14 ;
[0031] FIG. 16 is a schematic view of a CO2 extractor and algae culture according to the present invention including a shower; and
[0032] FIG. 17 is a schematic view of a CO2 extractor and algae culture similar to FIG. 16 .
Detailed Description of Preferred Embodiments
[0033] In broad concept, the present invention in one aspect extracts carbon dioxide from ambient air using a conventional CO2 extraction method or one of the improved CO2 extraction methods disclosed in our aforesaid PCT Applications, or disclosed herein, and releases at least a portion of the extracted CO2 to a closed environment.
[0034] In a first exemplary embodiment, this closed environment is a greenhouse. Preferably, but not necessarily, the CO2 extractor is located adjacent to the greenhouse and, in a preferred embodiment the extractor also provides shading for crops grown in greenhouses which are sensitive to strong sunlight, and/or reduces cooling requirements for the greenhouse.
[0035] In one approach to CO2 capture, the resin medium is regenerated by contact with the warm highly humid air. It has been shown that the humidity stimulates the release of CO2 stored on the storage medium and that CO2 concentrations between 3% and 10% can be reached by this method, and in the case of an evacuated/dehydrated system, close to 100% can be reached. In this approach the CO2 is returned to gaseous phase and no liquid media are brought in contact with the collector material.
[0036] The CO2 extractor is immediately adjacent to the greenhouse and is moved outside the greenhouse to collect CO2 and moved into the greenhouse to give off CO2. In such embodiment, the CO2 extractor preferably comprises a humidity sensitive ion exchange resin in which the ion exchange resin extracts CO2 when dry, and gives the CO2 up when exposed to higher humidity. A humidity swing may be best suited for use in arid climates. In such environment the extractor is exposed to the hot dry air exterior to the greenhouse, wherein CO2 is extracted from the air. The extractor is then moved into the warm, humid environment of the greenhouse where the ion exchange resin gives up CO2. The entire process may be accomplished without any direct energy input other than the energy to move the extractor from outside to inside the greenhouse and vice versa.
[0037] Ion exchange resins are commercially available and are used, for example, for water softening and purification. We have found that certain commercially available ion exchange resins which are humidity sensitive ion exchange resins and comprise strong base resins, advantageously may be used to extract CO2 from the air in accordance with the present invention. With such materials, the lower the humidity, the higher the equilibrium carbon loading on the resin.
[0038] Thus, a resin which at high humidity level appears to be loaded with CO2 and is in equilibrium with a particular partial pressure of CO2 will exhale CO2 if the humidity is increased and absorb additional CO2 if the humidity is decreased. The effect is large, and can easily change the equilibrium partial pressure by several hundred and even several thousand ppm. The additional take up or loss of carbon on the resin is also substantial if compared to its total uptake capacity.
[0039] There also seems to be an effect on humidity on the transfer coefficient, i.e. the reaction kinetics seem to change with changing humidity. However, the measured flux in and out of the resin seems to depend strongly on the difference between the actual partial pressure and the thermodynamic equilibrium pressure. As the equilibrium pressure changes with humidity, the size of the flux can be affected without an actual change in the reaction kinetics.
[0040] In addition, it is possible that kinetics is affected by other issues. For example, ion exchange materials which we have found to be particularly useful, are Anion I-200 ion exchange membrane materials available from Snowpure LLC, of San Clemente, Calif. The manufacturer describes Anion I-200 ion exchange membrane material as a strong base, Type 1 functionality ion exchange material. This material, which is believed made according to the U.S. Pat. No. 6,503,957 and is believed to comprise small resin charts encapsulated—or partially encapsulated—in an inactive polymer like polypropylene. We have found that if one first hydrates this material and then dries it, the material becomes porous and readily lets air pass through. The hydration/dehydration preparation is believed to act primarily to swell the polypropylene binder, and has little or no permanent effect on the resin, while the subsequent humidity swings have no observed impact on the polypropylene binder. We have found that these strong base ion exchange resin materials have the ability to extract CO2 from dry air, and give the CO2 out when humidity is raised without any other intervention. The ability of these materials to extract CO2 directly from the air, when dry, and exhale the CO2 as humidity is raised, has not previously been reported.
[0041] As noted supra, it is necessary to first hydrate this material and then dry it, before using, whereupon the material becomes porous and readily lets air pass through. Before hydration, the membrane material is substantially non-porous, or at least it is unable to permit passage of an appreciable amount of air through the membrane. However, after hydration and drying, the material is believed to undergo irreversible deformation of the polypropylene matrix during the resin swelling under hydration. Once the material has been deformed, the polypropylene matrix maintains its extended shape even after the resin particles shrink when drying. Thus, for substantially non-porous materials such as the Snowpure Ion Exchange material above described, it is necessary to precondition the material by hydrating and then drying the material before use.
[0042] We have observed a large change in the equilibrium partial pressure of CO2 over the resin with a change in humidity. Humidity either changes the state of the resin, or alternatively the entire system that needs to be considered is the CO2/H2O resin system. While not wishing to be bound by theory, it is believed that the free energy of binding CO2 to the resin is a function of the H2O partial pressure with which the resin is in equilibrium.
[0043] This makes it possible to have resins absorb or exhale CO2 with a simple swing in humidity without the need to resort to thermal swing and/or pressure swing, which would add to energy costs which could have an unfavorable effect with regard to the overall carbon dioxide balance of the system.
[0044] The amount of water involved in such a swing appears to be quite small. The possibility of a humidity swing also allows us to recover CO2 from an air collector with minimal water losses involved.
[0045] Other strong base Type 1 and Type 2 functionality ion exchange materials are available commercially from a variety of venders including Dow, DuPont and Rohm and Haas, and also advantageously may be employed in the present invention, either as available from the manufacturer, or formed into heterogeneous ion-exchange membranes following, for example, the teachings of U.S. Pat. No. 6,503,957.
[0046] FIG. 1 illustrates a first embodiment of our invention. A primary ion exchange filter material 4 is provided in a recirculation cycle. A primary pump 1 or a secondary pump (not shown) is used to remove the bulk of the air in the system while valve V1 is open and push it out through the air exhaust 2. At this point valve V1 is closed and a secondary ion exchange capture resin is switched into the system by opening valves V2 and V3. The secondary ion exchange resin can be utilized to provide humidity and possibly some heat. Warm steam stimulates the release of CO2 from the primary ion exchange filter material 4, which is then captured on the secondary ion exchange resin which is still out of equilibrium with the CO2 partial pressure. The volume of water in the system remains small as it is recirculated and not taken up by the secondary resin. While CO2 is unloading from the primary ion exchange resin material 14 and being absorbed by the secondary ion exchange resin, the bulk of the water cycles through the apparatus. The amount of water that can be devolved or absorbed is much smaller than the amount of CO2 that is transferred. At the end of the cycle the primary ion exchange filter material 14 is refreshed and the secondary ion exchange capture resin is loaded with CO2.
[0047] This system could be used to transfer CO2 from the air capture medium, e.g. an ion exchange resin onto a secondary resin without washing or wetting the primary resin. This has two advantages. First, the primary resin is not directly exposed to chemicals such as amines that were used in the past and described in our aforesaid PCT Application PCT/US061/029238. Second, we have seen that wet resins are ineffective in absorbing CO2 until they have dried out. It is therefore advantageous to avoid the wetting of the material and thus operate in this fashion where the resin is washed with low-pressure steam. Steam pressures could be less than 100 Pa and thus be saturated at temperatures similar to ambient values. However, the CO2 exchange is obviously accelerated at higher temperatures and higher steam pressures. The disadvantage of raising temperatures would be additional energy consumption.
[0048] The design outlined here is a special example of a broader class of designs where the secondary resin is replaced with any other sorbent material that is capable of absorbing CO2 without absorbing water. Such sorbents may include liquid amines, ionic liquids, solid CO2 sorbents such as lithium zirconate, lithium silicate, magnesium hydroxide or calcium hydroxide, or any of a wide class of chemical or physical sorbents capable of absorbing CO2 from a gas mixture including water vapor and CO2. The central concept is that of using a humidity swing, rather than a pressure or temperature swing to remove CO2 from the primary sorbent without bringing it in direct physical contact with a secondary sorbent.
Application in a Greenhouse for Improving Crop Yields
[0049] As noted supra, crop yield in greenhouses can be improved by increasing the carbon dioxide level in the greenhouse air. The present invention provides for the introduction of carbon dioxide into a greenhouse without combusting fuels emitting fossil fuel CO2 into the air. More particularly, we have found that we can employ humidity sensitive ion exchange resins to capture CO2 from dry outside air, and then release the CO2 into the greenhouse by exposing the resins to the warm moist greenhouse air.
[0050] In greenhouses located in warm in desert climates such as found in the Southwest United States, the outside CO2 loading may be performed at night when outside temperatures are cooler which may enhance CO2 uptake capacity. In cooler climates where greenhouses rely in part on radiative heating, our system of CO2 loading avoids the need to let in cold air to replenish the CO2 and thus reduces the need for heating employing fossil fuel consumption until temperatures drop so low that fuel based heating becomes necessary.
[0051] In one embodiment, we employ several filters made from humidity sensitive ion exchange active material. In one part of the cycle the filters are exposed to outside air that could be driven by natural wind flow, by thermal convection, or fans. It is preferable to avoid fans as they add an unnecessary energy penalty. In a second part of the cycle, moist air from inside the greenhouse preferably is driven through the filter material, e.g. by fans, which then releases CO2 into the greenhouse atmosphere. Since the climate control of the greenhouse typically will rely on a fan system anyway, there is little or no energy penalty.
[0052] Since plants at night respire, in some greenhouse designs it is possible to strip the CO2 from the greenhouse air by pulling the greenhouse air through the filters. The filters can then be exposed to higher humidity to facilitate the daytime release of the CO2 into the greenhouse.
[0053] In one embodiment, as shown in FIGS. 2A and 2B , the filter units 10 are located adjacent an exterior wall 12 of a greenhouse, and outside air or greenhouse air routed selectively therethrough, as the case may be, via pivotally mounted wall panels 14.
[0054] Alternatively, as shown in FIGS. 3A and 3B , the filter material 10 may be located exterior to and adjacent the roof 18 of the greenhouse, and outside air or greenhouse air routed selectively therethrough, as the case may be, via pivotally mounted roof panels 20.
[0055] In yet another embodiment of the invention, shown in. FIG. 4 , the filter units 10, can be moved from outside the greenhouse where they extract CO2 from the air to inside the greenhouse where they release the captured CO2. One possible option for doing this is to have filter units mounted to pivotally mounted wall or roof panels 22 which can be reversed so that a filter unit on the outside of the greenhouse is exposed to the inside of the greenhouse and vice versa. Filter units that are inside the greenhouse can have air blown through them by a fan system. Filter units on the outside are exposed to ambient air. In a preferred embodiment, shown in FIG. 4 , the filter units 10 on the outside are located adjacent the bottom end of a convection tower 24 that is solar driven. Preferably the inlets are installed at the bottom end of the convection towers where cool air enters and flows up the towers through natural convection.
[0056] In yet another embodiment, shown in FIG. 5 , the filter units 10 are moved in and out of the greenhouse, e.g. suspended from a track 26.
[0057] Referring to FIG. 6 , yet another option for a greenhouse is to locate convection towers as double glass walls on the outside of the greenhouse, and use the convection stream generated to collect CO2 on the outside. The double walls also serve to reduce the heatload on the interior during the day and thus reduce the need for air exchange which in turn makes it possible to maintain an elevated level of CO2 in the greenhouse. The double glass walls also reduce heat loss during the night.
[0058] In this example a protective glass surface 40 may be provided to keep some of the heat away from the main roof of the glass house 42, causing a convective flow 44 of ambient air over the roof surface. The flow of ambient air is passed through a CO2 absorbing filter medium 46, which can by some mechanism, such as a rotating roof panel 48, exchange places with a second like filter medium 50, where the air driven by fan 52 on the inside of the greenhouse is passed through the filter medium which gives up the CO2 captured when the filter medium was exposed to ambient air outside the greenhouse. Because the air inside the greenhouse is moist, the CO2 readily is released from the filter medium, and adds to the CO2 available in the greenhouse.
[0059] An advantage of such a unit is that it could operate at elevated levels of CO2 without combusting fuels. Because CO2 is delivered to the inside of the greenhouse without blowing air into the greenhouse, this offers a possibility of reducing the exchange of air between the outside and the inside of the greenhouse, thus improving the heat management and moisture management of the greenhouse.
[0060] In a second exemplary embodiment of the invention, the CO2 is extracted and delivered to an algal or bacterial bioreactor. This may be accomplished using conventional CO2 extraction methods or by using an improved extraction method as disclosed in our aforesaid PCT applications or disclosed herein; e.g., by a humidity swing. A humidity swing is advantageous for extraction of CO2 for delivery to algae because the physical separation allows the use of any collector medium without concern about compatibility between the medium and the algae culture solution. Transfer of gaseous CO2 allows for the selection of any algae species, including macro and microalgae, marine or freshwater algae. Therefore, the selection of algae species to be grown could be solely dependent on environmental factors and water quality at the collector site. For example, the algae species to be used could be selected from algae naturally occurring at the site, which are uniquely adapted to the local atmospheric, environmental and water quality conditions.
[0061] There are two major advantages of transferring captured CO2 in gaseous form. The first advantage is that the collector medium and/or the collector regeneration solution will not contact the algae culture solution and/or algae. The second is that all species of algae are capable of absorbing gaseous CO2.
[0062] Depending on the CO2 tolerance of particular algae cultures, the CO2-enriched air can be pumped successively through several algae cultures in order of decreasing CO2 tolerance and increasing CO2 uptake efficiency. Alternatively the air can be diluted to the optimum CO2 concentration.
[0063] Referring to FIG. 7 , one embodiment of the present invention takes advantage of the fact that gaseous CO2 can be driven off the collector medium using a humidity swing. The humidity swing will transfer captured CO2 as gaseous CO2 from the collector 110 into the algae culture 116. An ion-exchange collector medium loaded with CO2 will emit gaseous CO2 when subjected to an increase in humidity or when wetted with water. And the collector medium will absorb more gaseous CO2 when the humidity of the CO2-supplying gas stream is decreased and/or the collector medium dries.
[0064] The present invention provides a common headspace above the collector medium and the algae culture. This exposes the algae to gaseous CO2 while physically separating the collector medium from the algae culture solution. The headspace will be sealed from ambient air. The humidity is then raised in the closed headspace volume. Alternatively, the collector medium may be wetted. The CO2 emitted from the collector medium quickly diffuses through the entire headspace and contacts the algae culture solution surface.
[0065] The CO2 is then transferred into the algae culture either via gas diffusion or by bubbling the headspace gas through the algae culture solution using a recirculating pump. As the algae removes the CO2 from the headspace, the collector medium continues to offgas until equilibrium is reached. The algae culture solution can be mechanically stirred. All other nutrients and light are provided to the algae as needed. The algae may then be collected in an algae harvester 120.
[0066] CO2 concentrations in the headspace above wetted collector medium are up to 20%; or 0.2 atmosphere partial pressure. The concentration can be regulated by the volume to volume ratio of collector medium to headspace. Also the collector medium can release 60% of the captured CO2 during a humidity swing/wetting.
[0067] Alternatively, it is also possible to pump gas from the collector medium volume through the algae culture in order to transfer the CO2. If the algae pond is warm and moist the moisture from the algae pond may be sufficient to stimulate the release of CO2 from the dry resin, again by the humidity swing mechanism,
[0068] Referring to FIG. 8 , in another embodiment of the present invention CO2 concentrations in ambient air can saturate the ion-exchange medium with CO2 to the level that the CO2 is bound as bicarbonate anion. This embodiment provides regeneration of the collector medium using an alkaline solution. During the regeneration, the anion composition in the solution is changed to approximately 100% bicarbonate. Aqueous bicarbonate solution is not stable under atmospheric conditions and releases gaseous CO2. Gaseous CO2 emission can be enhanced by bubbling the headspace air through the solution using a recirculating pump.
[0069] An alternative embodiment provides a common headspace above the collector regeneration solution and the algae culture solution. This exposes the algae to gaseous CO2, while separating the regeneration solution from the algae culture solution. In other aspects, this headspace operates similar to the headspace for the collector medium, as discussed above.
[0070] Referring to FIG. 9 , another alternative embodiment of the present invention uses an electrodialysis (ED) process to free gaseous CO2 from the loaded collector solution. The freed CO2 is then transferred into an algae culture 216. The transfer of gaseous CO2 from the collector 210 to the algae culture 216 through an electrodialysis (ED) process has the advantage that the collector solution or sorbent and algae culture solution are physically separated from each other at all stages of the process. This prevents the mixing of the two solutions and also prevents ion exchange between the solutions. The ED process has this in common with the humidity swing process. And as in the humidity process, the physical separation allows the use of any collector medium and any algae without regard to compatibility between the medium and the algae culture solution.
[0071] An alternative embodiment of the invention takes advantage of the fact that gaseous CO2 can be driven off the collector regeneration solution using an ED process. In the ED process the loaded collector regeneration solution is split into two streams to enter the ED cell 214. Protons are added to the first stream across a secondary membrane 236 and the inorganic carbon is driven off as gaseous CO2, while the sodium cations are transferred through a cationic membrane 234 into the second stream. In addition to the sodium ions, hydroxide ions are added to the second stream across another secondary membrane 236 thus neutralizing the bicarbonate in this stream to carbonate.
[0072] The first stream exits the ED cell as water or dilute sodium bicarbonate solution while the second stream exits as a concentrated sodium carbonate solution. The two streams are combined to form fresh collector solution. The gaseous CO2 that is driven off the first stream is bubbled into the algae culture and is fixated as biomass.
[0073] As inorganic carbon is removed from the brine, the solution turns more alkaline and additional bicarbonate needs to be added to maintain the pH. Filtration allows us to recover some of the fluid and thus return water and sodium from the bioreactor. In one particular implementation the electrochemical cell will run between two separate fluid cycles, one fairly alkaline which runs between the collector and the base side of the electrochemical cell, and the other which runs at near neutral pH between the algae-reactor and the acidic side of the cell. Carbonic acid is transferred from the base side to the acid side of the cell. This step regenerates the wash and reloads the fluid with CO2.
[0074] By feeding the bicarbonate sorbent to the algae, CO2 can be removed from the sorbent without first converting the CO2 back to CO2 gas. Moreover, by selection of suitable sorbent material for the air capture side, the pH of the washing fluid can be kept relatively low, and if one uses algae that can tolerate a relatively high pH, the pH difference that needs to be made up by electrodialysis becomes relatively small, and in some implementations one can completely eliminate the dialysis cell.
[0075] Referring to FIG. 10 , another embodiment of the present invention uses an ED process to decrease the bicarbonate concentration in the collector solution and to increase the bicarbonate concentration in the algae culture solution. The collector solution enters the ED cell 214 in the bicarbonate state, while the algae culture solution enters the ED cell in the carbonate state. When the fluids exit the ED cell, the collector solution is in the carbonate state and the algae culture solution is in the bicarbonate state.
[0076] Since cations are transferred from the algae culture solution to the collector solution, the algae culture solution is diluted to roughly half its normality, while the collector solution roughly doubles its normality. To make up for the sodium imbalance, half of the loaded collector solution (bicarbonate form) is transferred directly from the collector to the algae culture.
[0077] In a process scheme according to the present invention, cations are transferred from the algae solution into the collector solution through a cation exchange membrane 234. The algae culture solution contains predominantly sodium cations, but also potassium, magnesium and calcium ions as well as traces of other metal cations. The potential transfer of magnesium and calcium is of concern, since both ions form fairly insoluble carbonates and hydroxides. The formation of these salts, also known as scaling, can foul up the membranes in the ED cell and/or the collector medium.
[0078] Calcium and magnesium are added to the algae culture as mineral nutrients, at the start of an algae growing cycle. As the algae biomass increases calcium and magnesium are taken up into the biomass and their concentration in the algae culture solution decreases. Simultaneously, the culture solution pH increases as the bicarbonate solution is changed into a carbonate solution. If magnesium, calcium and carbonate ions are present above their solubility products, chemical precipitation will further decrease the magnesium and calcium ion concentrations.
[0079] The exhausted culture solution with decreased calcium and magnesium concentrations and a high pH is entered into the ED cell. There the culture solution is changed from a carbonate into a bicarbonate solution and its pH decreases accordingly. As the carbonate ion concentration decreases, the solution can hold more calcium and magnesium. So scaling is unlikely to happen in this part of the ED cell.
[0080] However, at the same time, cations including calcium and magnesium are transferred from the algae culture solution 216 to the collector solution half-cell of the ED. In this half-cell, the bicarbonate solution coming from the collector is changed into a carbonate solution: the carbonate concentration and the pH increase. Further, excess H2O may be removed from the bicarbonate solution using an osmosis cell 224.
[0081] The process is designed such that the pH of the exiting collector solution is close to the pH of the incoming algae solution. Therefore, scaling should not occur as long as everything is in balance. However, to keep perfect balance may not always be practical on the macro scale, and it may be impossible on the micro scale within the ED cell. It is possible that micro layers or pockets with increased hydroxide or cation concentrations are formed at the membrane surfaces. Increased concentrations at the surface of the membranes might cause scaling in the collector solution half-cell.
[0082] To minimize scaling, the flux of calcium and magnesium cations has to be minimized. This is a problem well known in the manufacture of salt from seawater, sodium hydroxide manufacture, and in processing of skim milk by electro dialysis (T. Sata, 1972; T. Sata et al., 1979, 2001; J. Balster, 2006). To minimize flux, the cationic membrane that separates the two half-cells has to be monovalent ion selective. In general, strong acid cation exchange membranes show larger transport numbers for divalent than monovalent ions. It is assumed that this is due to higher electrostatic attraction with the negatively charged fixed ion exchange sites. The prior art has shown that transport numbers for divalent cations decrease with lower charge density on membranes.
[0083] Two commercially available highly monovalent cation selective membranes have been identified as particularly suited for this process. One membrane is manufactured by Asahi Glass and is traded under the name Selemion CSV. The second is manufactured by Tokuyama Soda and is sold under the name Neosepta® CIMS. The transport numbers (t) for Selemion CSV are: t(Na)<0.92 and t(Ca, Mg)<0.04. The transport numbers for Neosepta CIMS are t(Na,K)=0.90 and t(Ca, Mg)=0.10. The transport numbers are defined as the equivalence flux of the cation divided by the total equivalence flux during electrodialysis,
[0084] This aspect of the invention uses a monovalent cation selective membrane to minimize the transfer of multivalent cations from the algae culture solution into the collector regeneration solution. Any scaling built up with time, will be removed using an acid solution.
[0085] Both the algae culture solution as well as the collector solution will be filtered before entering the ED cell to avoid membrane fouling with particles. Organic molecules will be scavenged from the algae culture solution by means of organic scavenging ion exchange resins.
[0086] Referring to FIG. 11 , in another embodiment of the present invention the CO2 captured from air is transferred to the algae by feeding the loaded collector solution 310 to the algae. The loaded collector solution is enriched in sodium bicarbonate. Nutrients are added to the collector solution and it becomes the feed stock for algae. In this embodiment of the invention the solution feed is not recycled, so that the collector solution becomes a consumable.
[0087] In this process the algae culture solution 316 would increase in salt content as more and more sodium bicarbonate is added. The sodium bicarbonate is changed into carbonate during algae growth. To lower the carbonate concentration and to slow the salting, some of the remaining nutrients can be added as acids instead as sodium salts, which will convert carbonate ions to bicarbonate and minimize the addition of sodium.
[0088] Alternatively, the sodium bicarbonate sorbent is fed directly to an algae-reactor to supply the algae with CO2, and the algae is removed for further processing, with the sodium carbonate being returned to the air extraction station.
[0089] Many algae can utilize bicarbonate as their carbon source. Also, some algae prefer bicarbonate over CO2 as their carbon source. These are often algae that are indigenous to alkaline lakes, where inorganic carbon is predominantly present as bicarbonate. These algae can tolerate large swings in pH of 8.5 up to 11. Other algae can utilize HCO3− as their carbon source, but require pH ranges below pH=9, which would require bubbling CO2 through the bicarbonate/carbonate solution.
[0090] Algae use the carbon source to produce biomass through photosynthesis. Since photosynthesis requires CO2 not bicarbonate, the algae catalyze the following reaction:
HCO3−→CO2+OH−
HCO3−→CO2+OH−
[0091] In the presence of HCO3−, this becomes:
HCO3−+OH−→CO3−2+H2O
HCO3−+OH−→CO3−2+H2O
[0092] Algae growth in a bicarbonate solution induces the following changes in the solution: (1) a decrease in HCO3− concentration; (2) an increase in CO3−2 concentration; and (3) an increase in pH.
[0093] Another embodiment the present invention uses an algae culture solution for collector regeneration. The collector medium in the carbonate form can absorb gaseous CO2 from ambient air until the anion composition of the medium is nearly 100% bicarbonate. In this state the collector medium is fully loaded and CO2 absorption comes to a halt. A carbonate solution can be used in regeneration to return the loaded collector medium to a carbonate form through ion exchange. The anion composition of the regeneration solution can be changed from 100% carbonate to nearly 100% bicarbonate through anion exchange with the fully loaded collector medium. In a counter-flow regeneration process the collector medium can be brought into a carbonate form, while the carbonate regeneration solution is changed into a bicarbonate solution. The regeneration solution is fully loaded when it is in the bicarbonate form, since it cannot remove any more bicarbonate from the collector medium.
[0094] The algae are introduced into the process to remove the captured CO2 from the loaded regeneration solution by bicarbonate dehydration and neutralization (see above). The algae utilize the freed CO2 for biomass growth. And the regeneration solution is changed from bicarbonate back into a carbonate solution.
[0095] In this process, the carbonate regeneration solution and the collector medium are recycled, while ambient air CO2 is changed into algal biomass. This is shown in FIG. 11 .
[0096] This process provides a cycle in which the ion exchange collector medium absorbs air CO2. During the absorption the collector medium changes from carbonate to bicarbonate form. Then the regeneration solution pulls the air CO2 from the loaded collector medium. In this exchange the collector medium is changed back into its carbonate form, while the regeneration solution changes from a carbonate to a bicarbonate solution. Finally, the algae remove the air CO2 from the loaded regeneration solution by fixating it into biomass. In this step, the algae catalyze the reaction from bicarbonate to CO2 and carbonate. The CO2 carbon is bound into the algae biomass. The carbonate is left in solution. The resulting regeneration solution is then in carbonate form.
[0097] In another embodiment of the present invention, the algae culture solution is used as the collector regeneration solution. This means that the collector regeneration solution will in addition to carbonate contain other nutrients as required for the algae. Amongst these nutrients are anions that will compete with the carbonate anion during ion exchange with the collector medium.
[0098] In this process diatoms will not be used, since they require silica, which cannot be efficiently removed from the collector medium with a carbonate wash.
[0099] Other anionic nutrients typically found in algae culture mediums are: nitrate (NO3−), sulfate (SO4−2), and phosphate (PO4−3). Phosphorus may also be present as dibasic (HPO4−) or monobasic phosphate (H2PO4−) depending on pH.
[0100] Nitrate, sulfate and phosphate concentrations for typical algae culture mediums are:
[0101]
| Bold's Medium | Zarouk's Medium | ||
|---|---|---|---|
| Nutrient | Molarity (M) | Molarity (M) | |
| NaHCO3 | 0.2 | ||
| NaNO3 | 0.00882 | 0.029 | |
| MgSO4—7H2O | 0.0003 | 0.0008 | |
| FeSO4—7H2O | 0.0018 | ||
| K2SO4 | 0.0058 | ||
| Total S | Σ = 0.0003 | Σ = 0.0084 | |
| K2HPO4 | 0.00043 | 0.0029 | |
| KH2PO4 | 0.00129 | Σ = 0.0029 | |
| Total P | Σ = 0.00172 | ||
[0102] However, the prior art has shown that algae can grow at much lower nutrient concentrations than are contained in typical culture mediums.
[0103] To estimate the effect of the nutrient concentrations on the collector medium a nutrient-containing regeneration solution was mixed as follows: 0.14 M CO3−2, 0.04 M NO3−, 0.0017 M SO4−2 and 0.0017 M H2PO4−. These represent the highest concentrations to be found in an algae culture medium and, therefore the worst-case scenario.
[0104] The collector medium was then flushed with this ‘worst-ease’ solution until equilibrium was reached between the solution and the collector medium. At the pH of carbonate solution, phosphorus is present as dibasic phosphate (HPO4−2). Dibasic phosphate is basic enough to absorb CO2. Therefore, the presence of dibasic phosphate anions on the collector medium will not lower the medium's CO2 uptake capacity. It was determined that at equilibrium, about 50% of the collector medium's total exchange sites were occupied by carbonate and phosphate ions and 50% by nitrate and sulfate. Although the other nutrients outnumber carbonate, they do not completely replace it; instead, an anion equilibrium is reached that does not change with application of additional volumes of solution to the collector medium.
[0105] The experiments showed that in a worst-case scenario, the collector medium looses approximately 50% of its CO2 uptake capacity. However, as determined by the research cited above, the nutrient concentrations in the solution can be depleted significantly during algae growth. For example, nitrate being by far the most abundant nutrient after inorganic carbon, can be reduced to 0.002 M, a mere 5% of the concentration used in the worst-case scenario experiment. And phosphate is reduced to 45% of the worst-case scenario.
[0106] Further, a collector medium washed with a nutrient-depleted solution will loose about 20% of its CO2-uptake capacity. It is therefore possible to use the collector medium and wash it with a carbonate solution that has been derived from the algae growth medium.
[0107] The algae will secrete or release organic compounds into the solution during metabolism or decay. These organics will be scavenged from the solution, prior to applying the solution to the collector medium. Organics scavenging may be done with an adsorbent-type ion exchange resin or other processes.
[0108] Diatoms will not be used in this process, since they require silica, which cannot be efficiently removed from the collector medium using a carbonate wash.
[0109] A preferred algae for the present embodiment will have the following characteristics: they are adapted to high ionic strength liquids; they can grow in a pH range of 8.5 to roughly 11; they can tolerate a gradual pH change; they can use bicarbonate as their carbon source; they need little silica as a nutrient; they are capable of changing the pH of a solution from 8.5 to 11 or above; they can diminish nutrient concentrations to low levels; they can be used in biochemistry, agriculture, aquaculture, food, biofuels, etc.
[0110] Good candidates are, but are not limited to, algae that live in alkaline waters such as Spirulina platensis, Spirulina fusiformis, Spirulina sp., Tetraedron minimum and others.
[0111] There are many alternatives for this embodiment. Loaded collector solution (bicarbonate solution depleted in nutrients) is added to an algae culture together with fresh nutrients; the algal culture utilizes bicarbonate as its inorganic carbon source, by taking up about 50% of the bicarbonate carbon into its biomass and changing the remaining 50% to carbonate anions. Simultaneously, the algae culture depletes the nutrient concentrations in the solution. The culture is filtered, harvesting the algae biomass, while shunting the nutrient depleted solution towards the CO2 collector. The nutrient depleted solution is cleaned of organics and other materials deleterious to the collector medium. The solution now enriched in carbonate is used to regenerate the collector. In the process each carbonate anion is replaced by two bicarbonate anions, until the collector solution is loaded. The loaded collector solution is added to the algae culture together with fresh nutrients as mentioned above.
[0112] The process can be run as a continuous loop or a batch process, whichever is more practical given location, algae type, etc. The process can employ algae culturing technologies already in use and proven or new technologies. For example, outdoor ponds have proven successful for the cultivation of Spirulina, Chlorella vulgaris, Ankistrodesmus braunii and other species in California, Hawaii, the Philippines and Mexico among other places. According to the National Renewable Energy Laboratory (NREL), outdoor ponds, e.g. so-called “race ponds”, are the most efficient methods for growing a large biomass of algae.
[0113] The cultivation may use solar energy, artificial lighting or both dependent on the algae species and the place of operation. Algae culture solutions may be stirred to return algae to the zone of highest light ingress. Or the light might he brought into the algae cultures through mirrors, fiber optics and other means.
[0114] The algae can be either suspended in solution or immobilized. When suspended, algae follow their own growth patterns: single cells, colonies, clumped and so on. The natural growth pattern may not be the best match for the technology used. For example, small single celled algae may require elaborate harvesting processes.
[0115] Algae may naturally grow immobilized, if they attach themselves to surfaces, e.g., macro algae. Or algae can be immobilized: in beads using k-carragenan or sodium alginate, in polyurethane foam, on filter material, or as biofilms on column packing, or in other ways.
[0116] In an immobilized state, the algae may still be suspended, for example in bead form, and moving with the solution. Alternatively, the immobilized algae may be stationary in a column or other device, while the solution percolates past.
[0117] In another embodiment of the present invention, the collector medium is immersed into the Algae Culture. This can be done either in a batch process or in a continuous process. In a batch process, a batch of collector medium is alternatingly immersed in the algae culture and exposed to ambient air. In a continuous process, collector medium is continuously moved along a path on which it is alternatingly immersed in the algae culture or in exposed to air. The easiest implementation would be a disk of collector medium that rotates continuously around its center. The disk is submerged up to its center point in the algae culture, so that, at any time, one half of the collector medium is submerged in the liquid and the other half is exposed to air.
[0118] In this embodiment of the invention, collector medium could potentially be immersed in the algae culture solution at times of high nutrient content and at times of low nutrient content. The CO2 capacity of the collector medium will, therefore, range from 50% to 80% of its full capacity. Air exposure times can be adjusted to account for the capacity decrease.
[0119] Referring to FIG. 12 , another embodiment of the present invention discloses sodium bicarbonate transferred from the collector solution to the algae by washing the algae in the loaded collector solution. However, nutrients will not be added to the collector solution. Instead, nutrients will be provided to the algae via a second separate wash cycle consisting of nutrient-rich carbon deficient solution.
[0120] In this process the algae will be immersed in nutrient-deficient bicarbonate solution (loaded collector solution) alternating with inorganic carbon-deficient nutrient solution 326. A short rinse cycle will be employed between washes. The rinse will be added to the solution of the preceding wash.
[0121] The cycles of nutrient and bicarbonate washes will be optimized for the algae species used. One or more algae species may be used either mixed or in series to optimize the conversion of the bicarbonate solution (loaded collector solution) to carbonate solution (fresh collector solution). The fresh collector solution may be filtered to remove particles and cleaned of organic molecules or other deleterious content prior to application on the collector medium.
[0122] The process can be designed to utilize suspended algae or immobilized algae. If the algae are suspended, the process has to be run as a batch process, and the algae have to be filtered from the solution. To ease filtering the algae may be “immobilized” in suspended beads, in order to increase the particle size.
[0123] A process involving immobilized algae can utilize algae that naturally grow immobilized, for example macro-algae that attach themselves to surfaces, or micro-algae that form biofilms etc.
[0124] In addition to others methods disclosed elsewhere in this application, the algae could be immobilized in columns, inclined raceways, ponds or other containers. The containers may be arranged to allow gravitational fluid flow. Immobilization may be on the container walls and floors and/or on structures such as plates, packing etc. installed therein. Light is brought into the containers as needed either by natural lighting, artificial lighting, mirrors, fiber optics, etc.
[0125] Referring to FIG. 13 , another embodiment of the present invention transfers gaseous CO2 from the loaded collector solution 410 to the algae culture solution 416 through a hydrophobic microporous membrane 434. Gaseous CO2 can be transmitted from a bicarbonate solution through a hydrophobic membrane into a carbonate solution; and that the CO2 partial pressure differential between the two liquid streams is sufficient to drive the transfer. A transfer of water was noted from the more dilute solution to the more concentrated solution. As the membrane is hydrophobic, the transfer is of gaseous water molecules.
[0126] Simplified, the process can be described as two half-cells separated by a microporous, hydrophobic membrane. The first half cell 438 holds the loaded collector solution (sodium bicarbonate solution); while the second half cell 418 holds the algae culture (sodium carbonate solution including nutrients and algae).
[0127] The collector solution half-cell reaction is defined as follows:
2 HCO3-(aq)→CO2(g)+CO3−2(aq)+H2O
This is followed by CO2(g) diffusion through membrane into the algae culture half-cell. The reaction in the algae culture half-cell will follow in one of two ways:
Algae consume CO2(g)
or
CO3−2(aq)+CO2(g)+H2O→2 HCO3-(aq)
and
HCO3−(aq)+OH−→CO3−2(aq)+H2O
2 HCO3-(aq)→CO2(g)+CO3−2(aq)+H2O
This is followed by CO2(g) diffusion through membrane into the algae culture half-cell. The reaction in the algae culture half-cell will follow in one of two ways:
Algae consume CO2(g)
or
CO3−2(aq)+CO2(g)+H2O→2 HCO3-(aq)
and
HCO3−(aq)+OH−→CO3−2(aq)+H2O
[0128] As can be seen from the half-cell reactions, the pH in the collector solution will continuously increase as bicarbonate is reacted into carbonate through off-gassing of gaseous CO2. In a balanced system the algae culture solution will not change its pH as the gaseous CO2 is fixated by algae growth into biomass. The algae culture will preferably be close to a carbonate solution. In that case, it would not contain appreciable amounts of bicarbonate. This condition would maximize the gaseous CO2 partial pressure differential between the collector solution and the algae culture.
[0129] The physical arrangement of the two half-cells can take many forms including but not limited to the few arrangements described herein. Each arrangement will optimize the ratio of liquid-membrane contact area to solution volume. In general it is advantageous to run the collector solution through membrane channels submerged in the algae culture, since this will enable light supply to the algae culture. In cases where the algae culture is contained in membrane conduits, light will be supplied inside the conduits.
[0130] The membrane conduits can take many shapes. For example, they can be parallel membrane sheets, causing a sheet flow of solution sandwiched between the membranes. Or they could be tubular with the tube cross-section taking varying forms, for example round, square, rectangular, corrugated, etc. Tubes could form a spiral or other shapes to increase their path length through the solution.
[0131] The process can be run as a batch procedure, a continuous loop process or any combination thereof. Light and nutrients will be supplied as needed.
[0132] In a pure batch process, a batch of loaded collector solution is brought in membrane contact with a batch of algae culture and left to reach equilibrium.
[0133] In a pure continuous loop process both solutions flow in continuous loops. The loaded collector solution would flow along a membrane path, throughout which it transfers its gaseous CO2 to the algae solution; from there it enters the regeneration system for the collector medium, where it loads up with CO2 to then reenter the membrane conduit. The algae solution will flow past the membrane path with algae fixating the gaseous CO2; from there it will enter a harvesting system 420, where some or all algae are removed from the solution to then reenter the membrane system for renewed CO2 fixation and algae growth. Continuous flow or loop processes may use concurrent flow or counter-current flow of the two streams.
[0134] The major advantage of transferring the CO2 through a hydrophobic membrane is that ions cannot cross from the algae culture into the collector solution. The cations contained in the algae solution include earth alkali metals that can cause scaling along the collector solution path as the pH increases. The anions, such as nitrate and sulfate, contained in the algae solution compete with carbonate on the collector medium thus lowering the CO2 holding capacity of the collector medium. Therefore, it is advantageous to keep the ions from entering the collector solution. Since ions, which constitute the nutrients for the algae, cannot cross into the collector solution, the nutrient content of the algae culture can be permanently kept at the optimum concentration for algae growth.
[0135] In addition, the prior art discloses hydrophobic membranes that are also organophobic and can impede the transfer of organic molecules from the algae solution to the collector solution. Any organics that may be transferred into the collector solution will be removed from the collector solution before it enters the collector medium. For example, this can be done by scavenging the organic compounds onto ion exchange resins.
[0136] The membrane will be selected for its hydrophobicity, CO2 permeability, organophobicity, and water break-through pressure. The preferred algae for this process are those that thrive in carbonate solutions and can both utilize gaseous CO2 and bicarbonate. However, other algae can also be used to optimize the complete process.
[0137] Referring to FIG. 14 , another embodiment of the present invention transfers bicarbonate from the collector solution 410 into the algae culture solution 418 through an anion permeable membrane. The collector solution is brought into contact with one side of the anion permeable membrane 434, while the algae culture solution is brought into contact with the other side of the membrane.
[0138] The solutions exchange anions along concentration gradients. To optimize this ion exchange, the solutions can be run past the membrane in a counter-current. The solutions can also be run co-current to optimize other parts of the system. Alternatively, the process can be set up as a batch process rather than a continuous flow process.
[0139] The algae culture solution can be entered into the anion exchange process with algae suspended in the solution or without the algae. See FIG. 15 . Dissolved organic compounds can be removed from the algae culture solution prior to entering the membrane chamber.
[0140] Nutrient effects apply as discussed above. If the whole algae culture including algae is entered into the membrane exchanger, the nutrient concentration will be high and the collector solution will gain high nutrient concentrations. This may lead to a reduction in the collector medium's CO2 uptake capacity of up to 50%. If the culture solution without algae is entered into the membrane exchanger, the process can be set up such that nutrient-depleted solution is entered, in which case the collector capacity might be reduced by up to 20%.
[0141] Cations will not be exchanged between the two solutions, which greatly reduces the potential for scaling.
[0142] Alternatively, one can inject captured CO2 directly into an algae-bio-reactor synthetic fuel production unit. A particularly simple design is to provide a paddle wheel or disks or the like carrying humidity sensitive ion exchange resins that are exposed primarily above the water surface where CO2 is extracted from the air, and are slowly rotated to dip a portion under the water surface where the CO2 is released to provide high air-to-water transfer rates for the CO2.
[0143] Referring to FIG. 16 , in another embodiment it is possible to shower an ion exchange resin with slightly alkaline wash water at an extraction station 140, similar to the first exemplary embodiment, to make up evaporative or production losses of water from the bioreactor. As the wash water trickles over the primary resin, it will pick up bound CO2 and dribble it into the bioreactor system 142.
[0144] Alternatively, as shown in FIG. 17 , resins 142 may be added to the water at night to retain the CO2 that may be lost from the algae due to respiration. Thus we can improve the CO2 uptake efficiency of the algae, by preventing the release of nighttime CO2 from the bioreactor. In such embodiment, a secondary resin acts as a carbon buffer in the system. At night this buffer stores the CO2 released by the algae, while during the day it provides CO2 to the algae, while its CO2 content may be supplemented by the CO2 that is collected by the air collector. Once captured, the CO2 is transferred to the resin from a more concentrated wash used in regenerating the primary resin. Water filtration to keep algae out of the air collector generally is not a problem due to the fact that the air-side primary resin is designed to completely dry out in between cycles.
[0145] This transfer to the secondary resin also could be accomplished without direct contact in a low-pressure closed moist system, such as shown in FIG. 1 , by performing a humidity swing that avoids direct contact with the water. While such a system loses the aforementioned advantage of not bringing CO2 back to the gas phase, it will have other advantages in buffering the algae pond at a constant pH, without the use of chemicals.
[0146] In a preferred embodiment of the invention, as seen in FIG. 18 , in order to reduce water losses, increase yield, and better confine the algae, we employ bioreactors 150 with light concentrators 152. Such systems may be built from glass tubes surrounded by mirrors, or mirror or reflector systems that feed into fiber optic light pipes that distribute the light throughout a large liquid volume. The advantage of the use of a bioreactor with light concentrators is that they greatly reduce the water surface and thus reduce water losses. Thus, the CO2, can be collected nearby without directly interfering with the algae reactors. Indeed air collectors could take advantage of mirror systems for guiding air flows.
[0147] Algae typically fixate CO2 during times of light influx, and respire CO2 during dark cycles. The CO2 is captured by adding additional collector medium to the system in strategic places. The collector medium can, for example, be immersed in the algae culture. In this case, it will store bicarbonate and release carbonate during respiration as the culture solution pH decreases, and it will release bicarbonate and store carbonate during photosynthesis as the culture solution increases in pH.
[0148] Collector medium can also be placed in the air space in proximity of the algae culture to absorb CO2 that has been released from the culture solution. This will be especially efficient in closed structures. Collector medium placed in the proximity of the culture solution will be regenerated using one of the processes described above.
[0149] This application is intended to include any combination of the inorganic carbon transfer methods described in this patent using any combination of algae cultures as required to optimize the process. Optimization includes but is not limited to optimization of the carbon transfer efficiency, carbon transfer rate, market value of the biomass (for example oil content, starch content etc.), algae productivity efficiency, and algae growth rate under any climate conditions or climate-controlled conditions.
[0150] While the invention has been described in connection with a preferred embodiment employing a humidity sensitive ion exchange resin material for extracting CO2 from ambient air and delivering the extracted CO2 to a greenhouse by humidity swing, advantages with the present invention may be realized by extracting carbon dioxide from ambient air using a sorbent in accordance with the several schemes described in our aforesaid PCT Application Nos. PCT/US05/29979 and PCT/US06/029238, and releasing the extracted CO2 into a greenhouse by suitably manipulating the sorbent.
Claims
The invention claimed is:
1. An apparatus for the capture of CO2 from air comprising an anion exchange material that captures CO2 from a flow of air and from which captured CO2 is releasable by wetting or a swing in humidity; and a wetting or humidity source contained within an enclosure containing a growing biomass, wherein the anion exchange material is a movable filter that is moveable into and out of the enclosure.
2. The apparatus of claim 1, wherein said enclosure is a greenhouse.
3. The apparatus of claim 1, wherein said anion exchange material extracts CO2 when dry and releases CO2 when exposed to higher humidity.
4. The apparatus of claim 1, wherein the anion exchange material is a component of a heterogeneous ion exchange material.
5. The apparatus of claim 1, wherein the anion exchange material comprises a strong base resin.
6. The apparatus of claim 5, wherein said resin comprises a Type 1 or Type 2 functionality ion exchange resin.
7. The apparatus of claim 6, wherein said ion exchange resin comprises Anion I-200 ion exchange membrane material.
8. The apparatus of claim 1, further comprising a sorbent to which released CO2 is transferred.
9. The apparatus of claim 8, wherein said sorbent is selected from the group consisting of: a liquid amine, an ionic liquid, a solid CO2 sorbent, lithium zirconate, lithium silicate, magnesium hydroxide, and calcium hydroxide.
10. The apparatus of claim 8, wherein said sorbent comprises an ion exchange resin.
11. The apparatus of claim 1, wherein said anion exchange material comprises a material from which 60% of said captured CO2 is releasable by wetting or swing in humidity.
12. The apparatus of claim 1, wherein said apparatus is located adjacent a controlled environment into which captured CO2 is released.
13. The apparatus of claim 1, wherein said enclosure comprises a greenhouse.
14. The apparatus of claim 1, wherein said anion exchange material is cycled into and out of the enclosure.
Patent Citations (221)
| Patent | Date | Inventor | Cited By |
|---|---|---|---|
| US1482367(A) | 1924-01-01 | Elledge | Applicant |
| US2718454(A) | 1955-09-01 | Wylie | Applicant |
| US2796145(A) | 1957-06-01 | King | Applicant |
| US3024207(A) | 1962-03-01 | Shaw et al. | Applicant |
| US3063195(A) | 1962-11-01 | Ravich | Applicant |
| US3318588(A) | 1967-05-01 | Russell et al. | Applicant |
| US3330750(A) | 1967-07-01 | McRae et al. | Applicant |
| US3344050(A) | 1967-09-01 | Mayland et al. | Applicant |
| US3466138(A) | 1969-09-01 | Spiegler et al. | Examiner |
| US3489506(A) | 1970-01-01 | Galstaun et al. | Applicant |
| US3498026(A) | 1970-03-01 | Messinger et al. | Applicant |
| US3554691(A) | 1971-01-01 | Kuo et al. | Applicant |
| US3594989(A) | 1971-07-01 | Bastiaans | Applicant |
| US3627478(A) | 1971-12-01 | Tepper | Applicant |
| US3627703(A) | 1971-12-01 | Kojima | Applicant |
| US3645072(A) | 1972-02-01 | Clapham | Applicant |
| US3691109(A) | 1972-09-01 | Larsen | Applicant |
| US3710778(A) | 1973-01-01 | Cornelius | Applicant |
| US3712025(A) | 1973-01-01 | Wallace | Applicant |
| US3727375(A) | 1973-04-01 | Wallace | Examiner |
| US3833710(A) | 1974-09-01 | Deschamps et al. | Applicant |
| US3865924(A) | 1975-02-01 | Gidaspow et al. | Applicant |
| US3876565(A) | 1975-04-01 | Takashima et al. | Applicant |
| US3876738(A) | 1975-04-01 | Marinaccio et al. | Applicant |
| US3907967(A) | 1975-09-01 | Filss | Applicant |
| US3915822(A) | 1975-10-01 | Veltman | Applicant |
| US3948627(A) | 1976-04-01 | Schwarz et al. | Applicant |
| US3981698(A) | 1976-09-01 | Leppard | Applicant |
| US4012206(A) | 1977-03-01 | Macriss et al. | Applicant |
| US4047894(A) | 1977-09-01 | Kuhl | Applicant |
| US4167551(A) | 1979-09-01 | Tamura et al. | Applicant |
| US4197421(A) | 1980-04-01 | Steinberg | Applicant |
| US4238305(A) | 1980-12-01 | Gancy et al. | Applicant |
| US4239515(A) | 1980-12-01 | Yanagioka et al. | Applicant |
| US4246241(A) | 1981-01-01 | Mathur et al. | Applicant |
| US4296050(A) | 1981-10-01 | Meier | Applicant |
| US4340480(A) | 1982-07-01 | Pall et al. | Applicant |
| US4436707(A) | 1984-03-01 | Karwat | Applicant |
| US4475448(A) | 1984-10-01 | Shoaf et al. | Applicant |
| US4497641(A) | 1985-02-01 | Brown, Jr. et al. | Applicant |
| US4511375(A) | 1985-04-01 | BeVier | Applicant |
| US4528248(A) | 1985-07-01 | Galbraith et al. | Applicant |
| US4566221(A) | 1986-01-01 | Kossin | Applicant |
| US4592817(A) | 1986-06-01 | Chlanda et al. | Applicant |
| US4594081(A) | 1986-06-01 | Kroll et al. | Applicant |
| US4608140(A) | 1986-08-01 | Goldstein | Applicant |
| US4678648(A) | 1987-07-01 | Wynn | Applicant |
| US4711645(A) | 1987-12-01 | Kumar | Applicant |
| US4729883(A) | 1988-03-01 | Lam et al. | Applicant |
| US4770777(A) | 1988-09-01 | Steadly et al. | Applicant |
| US4804522(A) | 1989-02-01 | Hass | Applicant |
| US4810266(A) | 1989-03-01 | Zinnen et al. | Applicant |
| US4861360(A) | 1989-08-01 | Apffel | Applicant |
| US4869894(A) | 1989-09-01 | Wang et al. | Applicant |
| US4899544(A) | 1990-02-01 | Boyd | Applicant |
| US4906263(A) | 1990-03-01 | Von Blucher et al. | Applicant |
| US4941898(A) | 1990-07-01 | Kimura | Applicant |
| US5070664(A) | 1991-12-01 | Groh et al. | Applicant |
| US5180750(A) | 1993-01-01 | Sugaya et al. | Applicant |
| US5215662(A) | 1993-06-01 | Johnson et al. | Applicant |
| US5277915(A) | 1994-01-01 | Provonchee et al. | Applicant |
| US5281254(A) | 1994-01-01 | Birbara et al. | Applicant |
| US5308466(A) | 1994-05-01 | Ganzi et al. | Examiner |
| US5316637(A) | 1994-05-01 | Ganzi et al. | Examiner |
| US5318758(A) | 1994-06-01 | Fujii et al. | Applicant |
| US5344627(A) | 1994-09-01 | Fujii et al. | Applicant |
| US5385610(A) | 1995-01-01 | Deerer et al. | Applicant |
| US5389257(A) | 1995-02-01 | Todd et al. | Applicant |
| US5414957(A) | 1995-05-01 | Kenney | Applicant |
| US5454189(A) | 1995-10-01 | Graham et al. | Applicant |
| US5525237(A) | 1996-06-01 | Birbara et al. | Applicant |
| US5535989(A) | 1996-07-01 | Sen | Applicant |
| US5658372(A) | 1997-08-01 | Gadkaree | Applicant |
| US5682709(A) | 1997-11-01 | Erickson | Examiner |
| US5711770(A) | 1998-01-01 | Malina | Applicant |
| US5756207(A) | 1998-05-01 | Clough et al. | Applicant |
| US5779767(A) | 1998-07-01 | Golden et al. | Applicant |
| US5788826(A) | 1998-08-01 | Nyberg | Examiner |
| US5797979(A) | 1998-08-01 | Quinn | Examiner |
| US5887547(A) | 1999-03-01 | Caveny et al. | Applicant |
| US5914455(A) | 1999-06-01 | Jain et al. | Applicant |
| US5917136(A) | 1999-06-01 | Gaffney et al. | Applicant |
| US5934379(A) | 1999-08-01 | Ostlyngen et al. | Applicant |
| US5955043(A) | 1999-09-01 | Neuman et al. | Applicant |
| US5972080(A) | 1999-10-01 | Nagata | Applicant |
| US5980611(A) | 1999-11-01 | Kumar et al. | Applicant |
| US6004381(A) | 1999-12-01 | Rohrbach et al. | Applicant |
| US6027552(A) | 2000-02-01 | Ruck et al. | Applicant |
| US6083740(A) | 2000-07-01 | Kodo et al. | Applicant |
| US6117404(A) | 2000-09-01 | Mimura et al. | Applicant |
| US6136075(A) | 2000-10-01 | Bragg et al. | Applicant |
| US6180012(B1) | 2001-01-01 | Rongved | Applicant |
| US6221225(B1) | 2001-04-01 | Mani | Applicant |
| US6228145(B1) | 2001-05-01 | Falk-Pedersen et al. | Applicant |
| US6237284(B1) | 2001-05-01 | Erickson | Examiner |
| US6279576(B1) | 2001-08-01 | Lambert | Applicant |
| US6306803(B1) | 2001-10-01 | Tazaki | Applicant |
| US6316668(B1) | 2001-11-01 | King et al. | Applicant |
| US6334886(B1) | 2002-01-01 | Barnes, Jr. et al. | Applicant |
| US6346938(B1) | 2002-04-01 | Birbara et al. | Applicant |
| US6402819(B1) | 2002-06-01 | De Ruiter et al. | Applicant |
| US6503957(B1) | 2003-01-01 | Bernatowicz et al. | Examiner |
| US6547854(B1) | 2003-04-01 | Gray et al. | Applicant |
| US6582498(B1) | 2003-06-01 | Sass et al. | Applicant |
| US6617014(B1) | 2003-09-01 | Thomson | Applicant |
| US6632848(B2) | 2003-10-01 | Sugaya | Applicant |
| US6645272(B2) | 2003-11-01 | Lemaire et al. | Applicant |
| US6716888(B2) | 2004-04-01 | Bernatowicz et al. | Applicant |
| US6890497(B2) | 2005-05-01 | Rau et al. | Applicant |
| US6908497(B1) | 2005-06-01 | Sirwardane | Applicant |
| US6969466(B1) | 2005-11-01 | Starner | Applicant |
| US7067456(B2) | 2006-06-01 | Fan et al. | Applicant |
| US7132090(B2) | 2006-11-01 | Dziedzic et al. | Applicant |
| US7270796(B2) | 2007-09-01 | Kemp et al. | Applicant |
| US7343341(B2) | 2008-03-01 | Sandor et al. | Applicant |
| US7364608(B2) | 2008-04-01 | Tanahashi et al. | Applicant |
| US7384621(B2) | 2008-06-01 | Stevens et al. | Applicant |
| US7415418(B2) | 2008-08-01 | Zimmerman | Applicant |
| US7420004(B2) | 2008-09-01 | Hardy et al. | Applicant |
| US7655069(B2) | 2010-02-01 | Wright et al. | Applicant |
| US2001/0004895(A1) | 2001-06-01 | Preiss | Applicant |
| US2001/0009124(A1) | 2001-07-01 | Suzuki et al. | Applicant |
| US2001/0022952(A1) | 2001-09-01 | Rau et al. | Applicant |
| US2002/0083833(A1) | 2002-07-01 | Nalette et al. | Applicant |
| US2002/0102674(A1) | 2002-08-01 | Anderson | Examiner |
| US2002/0178925(A1) | 2002-12-01 | Mimura et al. | Applicant |
| US2003/0022948(A1) | 2003-01-01 | Seiki et al. | Applicant |
| US2003/0145726(A1) | 2003-08-01 | Gueret et al. | Applicant |
| US2003/0167692(A1) | 2003-09-01 | Jewell et al. | Applicant |
| US2003/0205692(A1) | 2003-11-01 | Fleming et al. | Applicant |
| US2003/0220188(A1) | 2003-11-01 | Marand et al. | Applicant |
| US2004/0031424(A1) | 2004-02-01 | Pope | Examiner |
| US2004/0069144(A1) | 2004-04-01 | Wegeng et al. | Applicant |
| US2004/0103831(A1) | 2004-06-01 | Pope | Applicant |
| US2004/0134353(A1) | 2004-07-01 | Gillingham et al. | Applicant |
| US2004/0195115(A1) | 2004-10-01 | Colombo | Applicant |
| US2004/0213705(A1) | 2004-10-01 | Blencoe et al. | Applicant |
| US2004/0219090(A1) | 2004-11-01 | Dziedzic et al. | Applicant |
| US2005/0011770(A1) | 2005-01-01 | Katsuyoshi et al. | Applicant |
| US2005/0063956(A1) | 2005-03-01 | Bernklau et al. | Applicant |
| US2005/0092176(A1) | 2005-05-01 | Ding et al. | Examiner |
| US2005/0095486(A1) | 2005-05-01 | Hamamoto et al. | Applicant |
| US2005/0204915(A1) | 2005-09-01 | Sammons et al. | Applicant |
| US2005/0252215(A1) | 2005-11-01 | Beaumont | Examiner |
| US2005/0269094(A1) | 2005-12-01 | Harris | Applicant |
| US2005/0279095(A1) | 2005-12-01 | Goldman | Examiner |
| US2006/0013963(A1) | 2006-01-01 | Thomson | Applicant |
| US2006/0042209(A1) | 2006-03-01 | Dallas et al. | Applicant |
| US2006/0051274(A1) | 2006-03-01 | Wright et al. | Applicant |
| US2006/0186562(A1) | 2006-08-01 | Wright et al. | Applicant |
| US2006/0249020(A1) | 2006-11-01 | Tonkovich et al. | Applicant |
| US2006/0289003(A1) | 2006-12-01 | Lackner et al. | Applicant |
| US2007/0004023(A1) | 2007-01-01 | Trachtenberg | Applicant |
| US2007/0149398(A1) | 2007-06-01 | Jones et al. | Applicant |
| US2007/0187247(A1) | 2007-08-01 | Lackner et al. | Applicant |
| US2007/0199448(A1) | 2007-08-01 | Yates et al. | Applicant |
| US2007/0217982(A1) | 2007-09-01 | Wright et al. | Applicant |
| US2008/0008793(A1) | 2008-01-01 | Forsyth et al. | Applicant |
| US2008/0025893(A1) | 2008-01-01 | Asprion et al. | Applicant |
| US2008/0031801(A1) | 2008-02-01 | Lackner et al. | Applicant |
| US2008/0087165(A1) | 2008-04-01 | Wright et al. | Applicant |
| US2009/0120288(A1) | 2009-05-01 | Lackner et al. | Applicant |
| US2009/0232861(A1) | 2009-09-01 | Wright et al. | Applicant |
| US2009/0294366(A1) | 2009-12-01 | Wright et al. | Applicant |
| CA1212522 | 1986-10-01 | Applicant | |
| CA1236877 | 1988-05-01 | Applicant | |
| DE4130837 | 1992-04-01 | Applicant | |
| DE19521678 | 1995-06-01 | Applicant | |
| DE19727295 | 1999-01-01 | Applicant | |
| DE19830470 | 1999-11-01 | Applicant | |
| DE20001385 | 2000-08-01 | Applicant | |
| EP20055 | 1980-12-01 | Applicant | |
| EP254137 | 1988-01-01 | Applicant | |
| EP585898 | 1994-09-01 | Applicant | |
| FR2.029.424 | 1970-10-01 | Applicant | |
| GB1004046 | 1965-09-01 | Applicant | |
| GB1031799 | 1966-06-01 | Applicant | |
| GB1031799 | 1966-06-01 | Applicant | |
| GB1109439 | 1968-04-01 | Applicant | |
| GB1204781 | 1970-09-01 | Applicant | |
| GB1296889 | 1972-11-01 | Applicant | |
| GB1520110 | 1974-10-01 | Applicant | |
| JP58-122022 | 1983-07-01 | Applicant | |
| JP6172035 | 1986-04-01 | Applicant | |
| JP61-254221 | 1986-11-01 | Applicant | |
| JP61-280217 | 1986-12-01 | Applicant | |
| JP6312323 | 1988-01-01 | Applicant | |
| JP6312324 | 1988-01-01 | Applicant | |
| JP63-016032 | 1988-01-01 | Applicant | |
| JP63-69525 | 1988-03-01 | Applicant | |
| JP63-69527 | 1988-03-01 | Applicant | |
| JP1-208310 | 1989-08-01 | Applicant | |
| JP1-305809 | 1989-12-01 | Applicant | |
| JP3-245811 | 1991-01-01 | Applicant | |
| JP4-200720 | 1992-07-01 | Applicant | |
| JP6-253682 | 1994-09-01 | Applicant | |
| JP2000-107895 | 2000-04-01 | Applicant | |
| JP2004-261757 | 2004-09-01 | Applicant | |
| JP2006-340683 | 2006-12-01 | Applicant | |
| JP2007-190529 | 2007-08-01 | Applicant | |
| RU511963 | 1976-06-01 | Applicant | |
| RU715120 | 1980-02-01 | Applicant | |
| RU2097115 | 1997-11-01 | Applicant | |
| SD1828406 | 1993-07-01 | Applicant | |
| WO98/16296 | 1998-04-01 | Applicant | |
| WO98/17388 | 1998-04-01 | Applicant | |
| WO98/22173(A) | 1998-05-01 | Applicant | |
| WO/50154 | 2000-08-01 | Applicant | |
| WO/76633 | 2000-12-01 | Applicant | |
| WO1/21269 | 2001-03-01 | Applicant | |
| WO2005/108297 | 2005-11-01 | Applicant | |
| WO2006/009600 | 2006-01-01 | Applicant | |
| WO2006/036396 | 2006-04-01 | Applicant | |
| WO2006/084008 | 2006-08-01 | Applicant | |
| WO2007/016271 | 2007-02-01 | Applicant | |
| WO2007/016274 | 2007-02-01 | Applicant | |
| WO2007/114991 | 2007-10-01 | Applicant | |
| WO2008/042919 | 2008-04-01 | Applicant | |
| WO2008/131132 | 2008-04-01 | Applicant | |
| WO2008/061210 | 2008-05-01 | Applicant | |
| WO2009/149292 | 2009-12-01 | Applicant |
Non-Patent Literature (147)
- Abstracts of Eos. Trans. AGU, 82 (47), Fall Meeting 2001; pp. 3.Applicant
- Abstracts of Eos. Trans. AGU, 83 (19), Spring Meeting 2002; pp. 3.Applicant
- Abstracts of Eos. Trans. AGU, 83 (47), Fall Meeting 2002; pp. 3.Applicant
- “An Industrial Sized Unit” Drawing and specification.Applicant
- Balster et al., “Multi-Layer Spacer Geometries With Improved Mass Transport”, 2006; pp. 351-361.Applicant
- Bituin, “New Findings May Redefine Renewable Energy Debate”, found at http://www.dailycal.org/article.php?id=8559, 2002.Applicant
- “Carbon Sequestration Could Be Employed Today to Help Alleviate Greenhouse Emissions” found at http://www.earthinstitute.columbia.edu/news/2003/story06-25-03b.html, 2003.Applicant
- Chinese Official Action dated May 5, 2010 and Jan. 20, 2011, Appln. No. 200680030297.X.Applicant
- Chinese Official Action dated Dec. 3, 2010, Appln. No. 200780008015.Applicant
- Choi et al. “A new preparation for cation-exchange membrane using monomer sorption into reinforcing materials” Desalination 146. Mar. 22, 2002.Applicant
- Choi et al. “Characterization of LDPE/polystyrene cation exchange membranes prepared by monomer sorption and UV radiation polymerization” Journal of Membrane Science 223 (2003) 201-215. Jul. 13, 2003.Applicant
- Choi et al. “Preparation and characterization of LDPE/polyvinvylbenzyl trimethyl ammonium salts anion-exchange membrane” Journal of Membrane Science 221 (2003) 219-231. Jun. 13, 2003.Applicant
- Cuiming et al. “Fundamental Studies of a New Hybrid (Inorganic-Organic) Positively Charged Membrane: Membrane Preparation and Characterizations” Journal of Membrane Science 216 (2003) 269-278 Feb. 16, 2003.Applicant
- Dow Chemical Company, Dowex Type 1 Strong Base Anion Resin, 1998, http://www.inaqua.de/Prod/ion/pdf—en/313—UPCORE—Mono—A625.pdf, p. 1.Applicant
- Dubey et al., “Chemical Extraction of Carbon Dioxide from Air to Sustain Fossil Energy by Avoiding Climate Change”, 2nd Annual Conference on Carbon Sequestration, 2003.Applicant
- Dubey et al., “Extraction of Carbon Dioxide from the Atmosphere Through Engineered Chemical Sinkage”, Fuel Chemistry Division Preprints, 2001; pp. 1-4.Applicant
- Dubey, “Science for Sustainability: From Capturing Carbon Dioxide From Air to Environmental Impact of a Hydrogen Economy”, found at http://www.mbari.org/seminars/2003/spring2003/apr2—dubey.html, 2003.Applicant
- Elliot et al., “Compensation of Atmospheric CO2 Buildup Through Engineered Chemical Sinkage”, pp. 1-8.Applicant
- Environment & Climate News, 2002; vol. 5, No. 7.Applicant
- Fuertes et al. “Carbon Composite Membranes from Matrimid and Kapton Polymides for Gas Separation” Microporous and Mesoporous Materials 33 (1999) 115-125 Jun. 16, 1999.Applicant
- Hashimoto et al., “Global CO2 recycling”, (1996) Zairyo to Kankyo/Corrosion Engineering, 45 (10), pp. 614-620 (Abstract only).Applicant
- Hensel, “In the Lab”, found at www.eponline.com/articles/53584, 2004.Applicant
- Information on David Keith found at http://www.ucalgary.ca/˜keith/.Applicant
- International Preliminary Report on Patentability, Dated Jan. 24, 2008 PCT/US2006/003646.Applicant
- International Preliminary Report on Patentability, mailed Jun. 10, 2010 PCT/US2007/063607.Applicant
- International Preliminary Report on Patentability, Aug. 11, 2009 PCT/US2009/053461.Applicant
- International Preliminary Report on Patentability, Aug. 24, 2009 PCT/US2009/054795.Applicant
- International Preliminary Report on Patentability, mailed Feb. 24, 2011, PCT/US09/53461.Applicant
- International Preliminary Report on Patentability, Nov. 15, 2007 PCT/US2007/084880.Applicant
- International Preliminary Report on Patentability, Jan. 27, 2009, PCT/US2007/84237.Applicant
- International Preliminary Report on Patentability, Oct. 20, 2009, PCT/US2008/60672.Applicant
- International Preliminary Report on Patentability, May 11, 2010, PCT/US2008/82505.Applicant
- International Preliminary Report on Patentability, Dec. 6, 2010, PCT/US2009/46306.Applicant
- International Preliminary Report on Patentability, Jun. 1, 2010, PCT/US2007/80229.Applicant
- International Preliminary Report on Patentability, Jan. 29, 2008, PCT/US2006/029238.Applicant
- International Search report and Written Opinion Feb. 2, 2006 PCT/US2006/003646.Applicant
- International Search report and Written Opinion Jul. 28, 2006 PCT/US2006/029238.Applicant
- International Search report and Written Opinion mailed Feb. 25, 2008 PCT/US2007/63607.Applicant
- International Search report and Written Opinion mailed Mar. 8, 2008 PCT/US2007/80229.Applicant
- International Search report and Written Opinion mailed Apr. 23, 2008 PCT/US2007/84880.Applicant
- International Search report and Written Opinion mailed Sep. 15, 2008 PCT/US2008/60672.Applicant
- International Search report and Written Opinion mailed Dec. 24, 2008 PCT/US2008/82505.Applicant
- International Search report and Written Opinion mailed Sep. 25, 2009 PCT/US2009/53461.Applicant
- International Search report and Written Opinion mailed Dec. 9, 2009 PCT/US2009/54795.Applicant
- International Search report and Written Opinion mailed Jan. 27, 2009 PCT/US2008/84237.Applicant
- International Search report and Written Opinion mailed Sep. 3, 2009 PCT/US2009/46306.Applicant
- International Search Report and Written Opinion dated Oct. 4, 2006 PCT/US05/29584.Applicant
- International Preliminary Report on Patentability dated Feb. 20, 2007 PCT/US05/29584.Applicant
- Japanese Official Action, Application Serial No. 2009-531567, dated Feb. 7, 2011, 4 pgs.Applicant
- Japanese Official Action, Application Serial No. 2008-524154, dated Feb. 16, 2011, 4 pgs.Applicant
- Keith et al., “Climate Strategy with CO2 Capture from the Air” 2005; pp. 1-43.Applicant
- Keith et al., “CO2 Capture From The Air: Technology Assessment and Implications for Climate Policy”, pp. 1-6.Applicant
- Keith et al., Resume of David Keith, Spring 2005, 8 pgs. “Climate Strategy with CO2 Capture From the Air”, found at http://ideas.repec.org/p/hal/papers/halshs-00003926—vl.html.Applicant
- Lackner et al., “Capturing Carbon Dioxide From Air”, pp. 1-15.Applicant
- Lackner et al., “Carbon Dioxide Extraction from Air?”, Arguments pp. 1-5.Applicant
- Lackner et al., “Carbon Dioxide Extraction from Air: Is It an Option?”, Proceedings of the 24th Annual Technical Conference on Coal Utilization and Fuel Systems, 1999; pp. 885-896.Applicant
- Lackner et al., “CO2 Extraction from Air” A White Paper from Los Alamos National Labs, The Reddy Corporation International, Sourcebook, Sep. 1999 (12 PGS).Applicant
- Lackner et al., “Free-Market Approaches to Controlling Carbon Dioxide Emissions to the Atmosphere: A Discussion of the scientific basis”, Los Alamos National Laboratory (Lackner & Ziock) & Harvard University (Wilson), pp. 1-16.Applicant
- Lackner et al., “The Case for Carbon Dioxide Extraction From Air,” Sourcebook, Sep. 1999; vol. 57, No. 9, pp. 6-10.Applicant
- Lackner K.S., Grimes P., Ziock H-J, ‘Capturing Carbon Dioxide from Air’ First National Conference on Carbon Sequestration (Washington) 2001.Applicant
- Lackner, Klaus S., “Can Fossil Carbon Fuel the 21st Century?”, International Geology Review, vol. 44, 2002, pp. 1122-1133.Applicant
- “Extraction CO2 from the Air”, Lackner presentation, 12 pages.Applicant
- Liang, “Carbon Dioxide Capture From Flue Gas Using Regenerable Sodium-Based Sorbents”, dated Aug. 1, 2003, Department of Chemical Engineering Thesis, (137 pgs).Applicant
- Liu et al., “Composite Membranes from Photochemical Synthesis of Ultrathin Polymer Films” Nature vol. 352 Jul. 4, 1991.Applicant
- Mexican Official Action, Dated Jan. 24, 2011, Serial No. MX/a/2007/002019.Applicant
- Mexican Official Action, Dated Feb. 2, 2011, Serial No. MX/a/2008/011464.Applicant
- Mizutani, Y “Structure of Ion Exchange Membranes” Journal of Membrane Science 49 (1990) 121-144 Aug. 21, 1989.Applicant
- Murdoch et al., “Sabatier Methanation Reactor for Space Exploration”, (2005) A Collection of Technical Papers—1st Space Exploration Conference: Continuing the Voyage of Discovery, 2, pp. 981-987 (Abstract only).Applicant
- “New Solutions to Oil Problems”, Whitley Strieber's Unknown Country, 2002, found at http://www.unknovvncountry.com/news/print.phtml?id=1467.Applicant
- Office Action dated Sep. 11, 2009 in U.S. Appl. No. 11/209,962.Applicant
- Office Action dated Feb. 23, 2010 in U.S. Appl. No. 11/209,962.Applicant
- Office Action dated Jun. 9, 2010 in U.S. Appl. No. 11/209,962.Applicant
- Office Action dated Aug. 27, 2010 in U.S. Appl. No. 11/209,962.Applicant
- Office Action dated Feb. 1, 2011 in U.S. Appl. No. 11/209,962.Applicant
- Office Action dated Oct. 1, 2009 in U.S. Appl. No. 11/227,660.Applicant
- Office Action dated Jan. 27, 2010 in U.S. Appl. No. 11/227,660.Applicant
- Office Action dated Oct. 7, 2010 in U.S. Appl. No. 11/227,660.Applicant
- Office Action dated Jan. 25, 2011 in U.S. Appl. No. 11/227,660.Applicant
- Office Action dated Mar. 30, 2009 in U.S. Appl. No. 11/346,522.Applicant
- Office Action dated Jun. 17, 2009 in U.S. Appl. No. 11/346,522.Applicant
- Office Action dated Oct. 7, 2009 in U.S. Appl. No. 11/683,824.Applicant
- Office Action dated Mar. 15, 2010 in U.S. Appl. No. 11/683,824.Applicant
- Office Action dated Jun. 28, 2010 in U.S. Appl. No. 11/683,824.Applicant
- Office Action dated Nov. 19, 2010 in U.S. Appl. No. 11/683,824.Applicant
- Office Action dated Nov. 10, 2010 in U.S. Appl. No. 11/996,615.Applicant
- Office Action dated Apr. 6, 2011 in U.S. Appl. No. 11/996,615.Applicant
- Office Action dated Nov. 9, 2010 in U.S. Appl. No. 12/638,717.Applicant
- Office Action dated Feb. 11, 2011 in U.S. Appl. No. 12/638,717.Applicant
- Office Action dated Mar. 11, 2011 in U.S. Appl. No. 12/903,962.Applicant
- Office Action dated Mar. 11, 2011 in U.S. Appl. No. 12/903,967.Applicant
- Office Action dated Mar. 11, 2011 in U.S. Appl. No. 12/903,970.Applicant
- Office Action dated Mar. 11, 2011 in U.S. Appl. No. 12/903,974.Applicant
- Office Action dated Mar. 11, 2011 in U.S. Appl. No. 12/903,981.Applicant
- Official Action dated Mar. 28, 2011 in U.S. Appl. No. 12/389,213.Applicant
- Official Action dated Mar. 15, 2010, U.S. Appl. No. 11/683,824, 10 pgs.Applicant
- Official Action for U.S. Appl. No. 11/209,962, dated Sep. 11, 2009, (16 pgs).Applicant
- Official Action issued in Applicants' counterpart Chinese Patent Application Serial No. 200680003905.8 dated Jun. 12, 2009.Applicant
- Official Action issued in Applicants' counterpart European Patent Application Serial No. 05 793 918.3-1213 dated Jan. 19, 2010.Applicant
- Official Action issued in Applicants' counterpart European Patent Application Serial No. 06 788 685.3-1213 dated Oct. 16, 2009.Applicant
- Official Action issued in Applicants' counterpart European Patent Application Serial No. 07 758 183.3 dated Jun. 22, 2010.Applicant
- Official Action issued in Applicants' counterpart European Patent Application Serial No. 07864483.8 dated Jan. 7, 2011.Applicant
- Official Action issued in Applicants' counterpart Russian Patent Application Serial No. 2008139902 (051576) dated Feb. 4, 2011.Applicant
- Official Action issued in Applicants' counterpart Russian Patent Application Serial No. 2008139902 dated Nov. 19, 2010.Applicant
- Official Action in Applicants' related Australian Patent Application Serial No. 2005290082 dated Apr. 20, 2007.Applicant
- Official Action in Applicants' related Australian Patent Application Serial No. 2005290082 dated Mar. 5, 2010.Applicant
- Official Action in Applicants' related Australian Patent Application Serial No. 2005290082 dated Apr. 13, 2010.Applicant
- Official Action in Applicants' related Australian Patent Application Serial No. 2005290082 dated May 20, 2010.Applicant
- Official Action in Applicants' related Australian Patent Application Serial No. 2005290082 dated Jul. 22, 2010.Applicant
- Official Action in related Australian Patent Application Serial No. 2006210619 dated Mar. 1, 2010.Applicant
- Official Action in Applicants' related Australian Patent Application Serial No. 2007233275 dated Jan. 14, 2011.Applicant
- Official Action in Applicants' related Australian Patent Application Serial No. 2007303240 dated Feb. 9, 2011.Applicant
- Official Action in Applicants' related New Zealand Patent Application Serial No. 575870 dated Mar. 17, 2011 and Nov. 11, 2010.Applicant
- “Researchers Explore Extracting CO2 Directly From Air” found at http://www.earthvision.net/ColdFusion/News—Page1.cfm?NewsID=20309.Applicant
- Resume of David Keith, Academic CV, Spring 2005, 8 pgs.Applicant
- Rickman, “Imagine No Restriction on Fossil-Fuel Usage and No Global Warming!”, found at http://www.lanl.gov/news/releases/archive/02-028.shtml.Applicant
- Russian Official Action +Translation, dated Feb. 2, 2006, Appln. No. 2007132880/15 (035886).Applicant
- Russian Official Action +Translation, dated Sep. 15, 2010 Appln. No. 2007132880/15 (035886).Applicant
- Russian Official Action +Translation, dated Feb. 11, 2010, Appln. No. 2007132880/15, (13 pgs).Applicant
- Singer, Fred S., “Americans Believe in Global Warming . . . and Psychic Powers, Astrology, and UFO's”, found at http://heartland.org/, 2002.Applicant
- Snowpure, LLC, SnowPure Excellion Product Information and Brochure, Aug. 2009.Applicant
- Sun et al., “CO2 sorption in activated carbon in the presence of water”, dated Feb. 9, 2007, Science Direct, Chemical Physics Letterse 437 (2000) (abstract enclosed).Applicant
- T.Sata, “Monovalent Cation Permselective Exchange Membrane”, Apr. 15, 1972, pp. 980-982.Applicant
- “The Carrot or the Stick: How to Build a Technology-Friendly Climate Policy in Canada” Presentation by David Keith, Climate Change Central Apr. 15, 2005, pp. 1-32.Applicant
- Toshikatsu Sata, “Modification of Properties of Ion Exchange Membranes. IV. Change of Transport Properties of Cation-Exchange Membranes by Various Polyelectrolytes”, 1978, pp. 1063-1080.Applicant
- Toshikatsu, Yukio Mizutani, “Modification of Properties of Ion Exchange Membranes. VI. Electrodialytic Transport Properties of Cation Exchange Membranes with a Electrodeposition Layer of Cationic Polyelectrolytes”, 1979, pp. 1199-1213.Applicant
- Toshikatsu, Yukio Mizutani, “Modification of Properties of Ion Exchange Membranes. VII. Relative Transport Number between Various Cations of Cation Exchange Membrane Having Cationic Polyelectrolyte Layer and Mechanism of Selective Permeation of Particular Cations”, 1979, pp. 2071-2085.Applicant
- Yin, et al., “Absorption and steam desorption performance of weak base anion exchange resin” (1995) Hangtian Yixue Yu Yixue Gongcheng/Space Medicine and Medical Engineering, 8 (1), pp. 27-31. (Abstract only).Applicant
- “Written Public Comments on the Strategic Plan for the U.S. Climate Change Science Program, General Comments”, 2003, pp. 1-160.Applicant
- Canadian Official Action dated Jun. 21, 2011, Appln. No. 2,577,685.Applicant
- Chinese Official Action dated Apr. 28, 2011 Appln. No. 200780042511.8.Applicant
- Chinese Official Action dated Jun. 13, 2011, Appln. No. 200780008015.0.Applicant
- Huang, Houping and Chang, Shih-Ger “Method to Regenerate Ammonia for the Capture of Carbon Dioxide” Energy and Fuels 2002, 16, 904-910.Applicant
- International Search Report and Written Opinion dated Nov. 24, 2010 GCC/P/2007/9020.Applicant
- Israel Official Action, Application Serial No. 25585/09, dated Jun. 30, 2011.Applicant
- Japanese Official Action, Application Serial No. 2008-524154, dated May 31, 2011, 3 pgs.Applicant
- Office Action dated Aug. 3, 2011 in U.S. Appl. No. 12/903,962.Applicant
- Office Action dated Aug. 1, 2011 in U.S. Appl. No. 12/903,974.Applicant
- Official Action dated Jul. 1, 2011 in U.S. Appl. No. 13/102,915.Applicant
- Official Action issued in Applicants' counterpart European Patent Application Serial No. 07 758 183.3-1213 dated Jul. 4, 2011.Applicant
- Official Action issued in Applicants' counterpart European Patent Application Serial No. 07 853 742.0-1213 dated Jul. 27, 2011.Applicant
- Official Action issued in Applicants' counterpart European Patent Application Serial No. 08 746 144.8-2113/2139584 dated May 9, 2011.Applicant
- Official Action issued in Applicants' counterpart Russian Patent Application Serial No. 2009116621/05 (022802) dated Jun. 1, 2011.Applicant
- Official Action received in Applicants' related Australian Patent Application Serial No. 2010241388 dated Jul. 7, 2011.Applicant
- Official Action received in Applicants' related Australian Patent Application Serial No. 2007319211 dated Jun. 17, 2011.Applicant
- Official Action received in Applicants' related Australian Patent Application Serial No. 2007233275 dated Jun. 1, 2011.Applicant
- Official Action received in Applicants' related Mexican Patent Application Serial No. MX/a/2007/009081, dated Jul. 18, 2011.Applicant
- Official Action received in Applicants' related New Zealand Patent Application Serial. No. 575870 dated Jun. 27, 2011.Applicant