Systems and methods for removal of carbon dioxide from seawater
11407667 · 2022-08-09
Inventors
Cpc classification
B01D2325/02
PERFORMING OPERATIONS; TRANSPORTING
B01D61/00
PERFORMING OPERATIONS; TRANSPORTING
B01D69/02
PERFORMING OPERATIONS; TRANSPORTING
B01D53/265
PERFORMING OPERATIONS; TRANSPORTING
B01D2311/04
PERFORMING OPERATIONS; TRANSPORTING
B01D71/70
PERFORMING OPERATIONS; TRANSPORTING
C02F9/00
CHEMISTRY; METALLURGY
C02F1/20
CHEMISTRY; METALLURGY
C02F1/001
CHEMISTRY; METALLURGY
International classification
C02F9/00
CHEMISTRY; METALLURGY
C02F1/20
CHEMISTRY; METALLURGY
B01D69/02
PERFORMING OPERATIONS; TRANSPORTING
Abstract
The present invention generally relates to a system and methods for the separation and removal of carbon dioxide from seawater. The system includes an extraction system that collects carbon dioxide from the seawater through a medium, and removes carbon dioxide from the medium; the extraction system comprising a reactor and a membrane. Alternatively, the extraction system includes a reactor, a membrane and a catalyst.
Claims
1. A method of separating and removing carbon dioxide from seawater in an extraction system comprising: a reactor; and a membrane, the method comprising the steps of: a) pumping seawater into the extraction system forming filtered seawater; b) filtering the seawater to remove solids; c) pumping the filtered seawater into the reactor; d) exposing the filtered seawater to the membrane; e) allowing the filtered seawater to flow back and forth across the membrane until equilibrium is established, whereby carbon dioxide and water vapor form in an air gap; f) evacuating the air gap above the filtered seawater to remove the carbon dioxide and water vapor; g) separating the carbon dioxide and water vapor in a cooler; and h) sequestering the carbon dioxide.
2. The method according to claim 1, further comprising the step of subjecting the filtered seawater to a catalytic enzyme after the step of exposing the filtered seawater to the membrane.
3. The method according to claim 2, wherein the catalytic enzyme is carbonic anhydrase.
4. The method according to claim 1, wherein the membrane comprises a membrane material having pores with sizes from about 4 angstroms to about 40 angstroms.
5. The method according to claim 4, wherein the membrane material comprises silicone.
6. The method according to claim 5, wherein the membrane material is polydimethylsiloxane.
7. A method of separating and removing carbon dioxide from seawater in an extraction system, the method comprising the steps of: a) pumping seawater into the extraction system forming filtered seawater; wherein the extraction system comprises a reactor, a membrane having pores with sizes from about 4 angstroms to about 40 angstroms and a catalytic enzyme; b) filtering the seawater to remove solids; c) pumping the filtered seawater into the reactor; d) exposing the filtered seawater to the membrane; e) subjecting the filtered seawater to the catalytic enzyme; f) allowing the filtered seawater to flow back and forth across the membrane until equilibrium is established, whereby carbon dioxide and water vapor form in an air gap; g) evacuating the air gap above the filtered seawater to remove the carbon dioxide and water vapor; h) separating the carbon dioxide and water vapor in a cooler; and, i) sequestering the carbon dioxide.
8. The method according to claim 7, wherein the catalytic enzyme is carbonic anhydrase.
9. The method according to claim 7, wherein the membrane comprises silicone.
10. The method according to claim 7, wherein the membrane comprises polydimethylsiloxane.
11. The method according to claim 7, further comprising a step of desalinating the filtered seawater.
12. The method according to claim 1, wherein the membrane comprises a membrane material permeable to carbon dioxide and water.
13. The method according to claim 1, wherein the membrane material comprises silicone.
14. The method according to claim 2, wherein the catalytic enzyme converts bicarbonate ion into dissolved carbon dioxide.
15. The method according to claim 7, wherein the catalytic enzyme converts bicarbonate ion into dissolved carbon dioxide.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1) In order to describe embodiments of the present invention more fully, reference is made to the accompanying drawings. These drawings are not to be considered limitations in the scope of the invention, but are merely illustrative.
(2)
(3)
(4)
(5) These and other features, aspects, and advantages of the present invention will become better understood with reference to the following description.
DETAILED DESCRIPTION OF EMBODIMENTS
(6) The description and the drawings of the present disclosure focus on one or more preferred embodiments of the present invention, and describe exemplary optional features and/or alternative embodiments of the present invention. The description and drawings are for the purpose of illustration and not limitation. Those of ordinary skill in the art would recognize variations, modifications and alternatives which are also within the scope of the invention.
(7) The present invention generally relates to a system and methods for separating, reduction and removal of carbon dioxide from seawater. The system includes an extraction system that collects carbon dioxide from the seawater through a medium, and removes carbon dioxide from the medium; the extraction system comprises a reactor, a membrane and a catalyst.
(8) The present invention addresses the aforementioned need for the reduction of carbon dioxide in the atmosphere by conversion of bicarbonate ion in seawater into carbon dioxide (CO.sub.2).
(9) Preferably a catalytic enzyme is used. More preferably, the enzyme is catalyzed by enzyme carbonic anhydrase. According to an embodiment of the present invention, carbon dioxide is removed by partial evacuation.
(10) In an embodiment of the present invention, a system and a method is provided to remove carbon dioxide from the ocean. According to a preferred embodiment, the system and methods reply on a natural equilibrium between dissolved and atmospheric carbon dioxide, which constantly strive to be reestablished, pulling carbon dioxide out of the air and dissolving it in the ocean.
(11) Given the density of air, (1.2 g/L), and the molecular weight of CO.sub.2, (44.01 g/mol), the 415 ppm concentration of CO.sub.2 in the atmosphere corresponds to 1.13×10.sup.−5 mol/L (M). Typically, approximately half of the CO.sub.2 generated by combustion during for example, incineration, dissolves into oceans, where some of it can react to form carbonic acid. Most of the acid typically dissociates to bicarbonate ions, and some of that further dissociates to carbonate ion:
CO.sub.2+H.sub.2O←.fwdarw.H.sub.2CO.sub.3←.fwdarw.H++HCO.sub.3.sup.−←.fwdarw.2H.sup.+CO.sub.3.sup.−2 Equation 1
(12) It is known to those skilled in the art that most of the carbon in the ocean (approximately 89%) is in the form of bicarbonate, HCO.sub.3.sup.−. Typically, the bicarbonate concentration is 2.38×10.sup.−3 M, which is approximately 211 times the concentration of CO.sub.2 in air. It is well known to those skilled in the art that it can be easier to remove a species from a mixture selectively if that species' concentration is higher.
(13) Typically, the H.sup.+ ions given off by carbonic acid are responsible for the acidification of the ocean, with its concomitant destruction of the bottom of the food chain as well as coral reefs. Selective removal of bicarbonate will therefore also mitigate the destruction being caused by ocean acidification.
(14) As can be appreciated, the double arrows in Equation 1 indicates that all the reactions are reversible, (forward and backward reactions happening continuously in equilibrium). Typically, if one of the species in the mixture is selectively removed from the system, the reactions adjust according to Le Chatelier's Principle to reform and reestablish equilibrium. Therefore, selective removal of bicarbonate will result in more CO.sub.2 moving from the atmosphere into the ocean to compensate, thus lowering atmospheric CO.sub.2. The same effect will occur by partially evacuating a sample of seawater so that dissolved CO.sub.2 bubbles out; the chemistry will adjust to restore dissolved CO.sub.2 when the sample is pumped back into the sea.
(15) According to a preferred embodiment of the present invention, the system and methods of restoring equilibrium can be speeded up by a catalyst. Typically the catalyst is an enzyme. More preferably, the catalytic enzyme is carbonic anhydrase (an enzyme used in many living things to maintain pH balance, by speeding up forward and reverse reactions). Typical applications for carbonic anhydrase have been used for the reverse of the present invention: to speed up conversion of CO.sub.2 and water to bicarbonate and H.sup.+ so that CO.sub.2 may be captured from flue gas in for example, fossil fuel power plants before being emitted into the air.
(16) Referring now to
(17) In alternative embodiment of the present invention, the system can further include a catalyst. Preferably, the catalyst is a catalytic enzyme capable of boosting carbon-capture kinetics of bicarbonate. More preferably, the catalytic enzyme is carbonic anhydrase. Carbonic anhydrase is known to those skilled in the art to speed up the formation of bicarbonate by a factor of 10.sup.7.
(18) Next, the filtered seawater 116 flows into the reactor chamber 118. Typically, the reactor chamber 118 can be any reactor chamber which is a tank known to those skilled in the art and
(19) According to an embodiment of the present invention, typically, the reactor 118 can be a batch or continuous flow reactor. Preferably, the reactor 118 is a reactor chamber capable of holding liquid and capable of removing gases (for example, air) above the seawater by evacuation.
(20) In yet a most preferred embodiment of the present invention, part of the reactor 118 contains a membrane 120. Typically, the membrane can be made of any membrane material known to those skilled in the art. Preferably, the membrane material allows some of the gases to be pumped out more easily than others. For example, silicone (polydimethylsiloxane) has a permeability coefficient that is much higher for CO.sub.2 than it is for nitrogen, oxygen or argon; only water moves through silicone more efficiently. In yet an alternative embodiment of the present invention, the membrane is hydrophilic. In yet another alternative embodiment of the present invention, the membrane material can be selected from the group consisting of polyvinylidene difluoride, polyether sulfone, cellulose acetate, cellulose nitrate nylon, and glass microfiber.
(21) Preferably, the membrane 120 is a membrane degasser, through which liquids such as water and gases can flow, but are impermeable to larger molecules like enzymes. Such membranes have pore sizes between about 4 and about 40 angstroms. According to an embodiment of the present invention, the pore size does not necessarily have to uniform and can be random.
(22) According to an embodiment of the present invention, the reactor chamber 118 contains a solution 122 between a wall of the reactor chamber 118 and the membrane 120. In a most preferred embodiment of the present invention, the solution 122 contains the catalyst of the system 100 for more efficient and quicker re-establishment of equilibrium. According to an embodiment of the present invention the catalyst is a catalytic enzyme. More preferably, the catalytic enzyme can be any one of the various carbonic anhydrases found in animals and plants.
(23) According to a yet preferred embodiment of the present invention, the filtered seawater 116 permeates freely back and forth across membrane 120 during its residence time in the reactor 118, rapidly establishing equilibrium between all species in Equation 1. Next, an air gap 124 above the filtered seawater 116 is partially evacuated by a vacuum pump through a port 126.
(24) Typically, the gases pumped out of the seawater in the air gap 124 of the reactor 118 will be a mixture of the major atmospheric gases: water vapor, CO.sub.2, nitrogen, oxygen and argon.
(25) According to a most preferred embodiment of the present invention, when silicone is used as the membrane material, the gases pumped out of the seawater will most likely be completely water vapor and CO.sub.2. These two gases can be easily separated, either by temperature or by adsorbents, so that once the water is stripped out, there should be no need for further gas separation before sequestration, although that always remains an option if desired.
(26) According to yet another preferred embodiment of the present invention, carbon dioxide and water are pulled out through the port 126 and are separated at a cooler 128, where the water condenses and is then directed to an output of the reactor 130 which typically leads out to sea. Next, the remaining CO.sub.2, preferably is pumped off to be compressed into cylinders ready for sequestration 132. In yet another preferred embodiment of the present invention a sequestration system that isolates the removed carbon dioxide to a location for at least one of storage and which can increase availability of renewable energy or non-fuel products (fertilizers and construction materials) and one or more energy sources that supply methods (heat) to the air extraction system to remove the carbon dioxide from the medium and which can regenerate it for continued used.
(27) In yet another embodiment of the present invention, additionally, pumps can be utilized.
(28) Referring now to
(29) In still yet another embodiment of the present invention, the aforementioned system and methods can be scaled up and much more elaborate. For example, during membrane degassing, the surface area of the membrane interface can be greatly increased by use of multiple columns of the membrane polymer.
(30) In yet another embodiment of the present invention, the utilization of temperature control can be used to maximize the rate of degassing. As water is heated, the solubility of carbon dioxide decreases, so that more gas bubbles out.
(31) In still yet another embodiment of the present invention, methods for separation of the extracted carbon dioxide from the water vapor could be applied that would also be pumped out of the reactor.
(32) Referring to the system and methods in
(33) According to an embodiment of the present invention, the cycle continues while the seawater is in the reactor. When the water is returned into the ocean, the water preferably has been depleted of both CO.sub.2 and bicarbonate, which causes it to absorb CO.sub.2 from the atmosphere to restore the equilibrium.
(34) According to yet another embodiment of the present invention, this method preferably requires an energy source. Preferably, the energy source is electrical. In order for the methods to create a net removal of CO.sub.2 from the ocean, preferably the reactor's electric power comes from carbon-free sources to ensure that the CO.sub.2 emitted during electrical power generation from the energy source is less than the amount of CO.sub.2 removed according to the methods of the present invention. Preferable carbon-free energy sources can be nuclear, solar, wind or hydroelectric. According to an embodiment of the present invention, reactors employing the methods of removing CO.sub.2 can be deployed to coastal areas that contract for clean energy or have their own dedicated solar panels.
(35) In a still further alternative embodiment of the present invention as shown in
(36) In summary, the present invention provides a system and method to remove carbon dioxide from seawater that is quick, efficient, not time consuming and inexpensive. Advantages of the system and methods according to preferred embodiments of the present invention over direct air capture methods since the preferred systems and methods disclosed utilizes the natural equilibrium already present in the environment. Typically, the concentration of carbon in seawater is much higher than in the air, and thus can be pulled out more efficiently. Natural equilibrium typically causes the ocean to absorb CO.sub.2 from the atmosphere if it is removed from seawater. The advantages of these preferred embodiments of the systems and methods of the present invention takes advantage of the already natural equilibrium occurring, over for example, electrochemical methods, since the methods and systems disclosed do not require energy to drive the chemical reaction. The methods and systems disclosed simply utilizes the natural equilibrium, accelerated by a natural catalyst, to separate the desired component, in this case carbon dioxide.
(37) Throughout the description and drawings, example embodiments are given with reference to specific configurations. It can be appreciated by those of ordinary skill in the art that the present invention can be embodied in other specific forms. Those of ordinary skill in the art would be able to practice such other embodiments without undue experimentation. The scope of the present invention, for the purpose of the present patent document, is not limited merely to the specific example embodiments or alternatives of the foregoing description.