DIRECT AIR CARBON CAPTURE CATALYST SYSTEM
20230398490 · 2023-12-14
Inventors
Cpc classification
B01D53/229
PERFORMING OPERATIONS; TRANSPORTING
B01D53/30
PERFORMING OPERATIONS; TRANSPORTING
B01D53/8671
PERFORMING OPERATIONS; TRANSPORTING
International classification
B01D53/30
PERFORMING OPERATIONS; TRANSPORTING
Abstract
A direct air carbon capture catalyst system wherein using direct air capture, combined with electrolysis of water and molecular separation, leftover carbon dioxide may undergo a hydrogenation process in a catalyst reactor to produce a desired hydrocarbon as a product, while storing other components of air, such as nitrogen and oxygen separated in earlier steps as side products.
Claims
1. A direct carbon capture catalyst system comprising: an air compressor that receives ambient air; one or more vapor filters that filter out water vapor in the ambient air; at least one ball valve positioned after the one or more vapor filters to shut down gas flow to the system; a flow meter that provides flow feedback measurements for gases moving from the compressor; a nitrogen membrane that filters out nitrogen, wherein the nitrogen passes through the at least one ball valve to a nitrogen storage tank; at least one oxygen membrane that receives an air mixture excluding the separated nitrogen to filter out oxygen, wherein the oxygen passes through the at least one ball valve to an oxygen storage tank; an electrolysis chamber that receives water and produces hydrogen gas; and a reactor that receives (1) a remaining air mixture including carbon dioxide and excluding the filtered oxygen and (2) hydrogen gas produced in the electrolysis chamber, wherein the carbon dioxide and hydrogen gas react at temperatures of approximately 400 degrees Celsius to produce hydrocarbons.
2. The system of claim 1, wherein hydrocarbons are produced using a catalyst core, wherein the catalyst core is Ni/Al.sub.2O.sub.3 or a combination of rhodium, iron, nickel, cobalt, molybdenum, iridium, palladium, platinum, or ruthenium for methanation of CO.sub.2 and then P-doped graphitic carbon nitride or P-doped g-C.sub.3N.sub.4 (CNP) to achieve direct photocatalytic methane conversion into ethanol under ambient conditions using CNP.
3. The system of claim 1, wherein hydrocarbons are produced using a catalyst core, wherein the catalyst core is Ni/Al.sub.2O.sub.3 or a combination of rhodium, iron, nickel, cobalt, molybdenum, iridium, palladium, platinum, or ruthenium for methanation of CO.sub.2 and then conversion of methane into methanol and ethanol over nickel oxide on a ceria-zirconia catalyst.
4. The system of claim 1, wherein hydrocarbons are produced using a catalyst core, wherein the catalyst core is Ni/Al.sub.2O.sub.3 or a combination of rhodium, iron, nickel, cobalt, molybdenum, iridium, palladium, platinum, or ruthenium for methanation of CO.sub.2 and then CO.sub.2 reduction to CO via a Ni—NS—C catalyst to produce CO using H.sub.2 collected from electrolysis and methane generated to make syngas.
5. The system of claim 1, wherein the hydrocarbons are stored.
6. The system of claim 1, wherein the hydrocarbons are compressed.
7. The system of claim 1 further comprising: a regulator that allows for direct use of the hydrocarbons.
8. The system of claim 1 further comprising: one or more solar panels that heat the reactor.
9. The system of claim 1 further comprising: an atomizer injection unit.
10. The system of claim 1 further comprising: one or more filters to prevent entry of unwanted materials to the nitrogen membrane and/or at least one oxygen membranes.
11. The system of claim 1 further comprising: at least one needle valve.
12. A method for direct carbon air capture using a catalyst system, the method comprising: receiving ambient air through an air compressor; separating out nitrogen and oxygen from ambient air using one or more membranes resulting in leftover carbon dioxide; storing the separated nitrogen and oxygen; and using a hydrogenation process on leftover carbon dioxide in a catalyst reactor to produce hydrocarbon end products.
13. The method of claim 12 further comprising: using one or more vapor filters, filtering out water vapor in the ambient air before separating out nitrogen and oxygen.
14. The method of claim 12, wherein the separated nitrogen passes through a ball valve to a nitrogen storage tank for storage.
15. The method of claim 12, wherein the separated oxygen passes through a ball valve to an oxygen storage tank for storage.
16. The method of claim 12 further comprising: producing hydrogen gas for the hydrogenation process in an electrolysis chamber.
17. The method of claim 12, wherein the hydrogenation process occurs at temperatures of approximately 400 degrees Celsius in a catalyst core.
18. The method of claim 17, wherein the catalyst core is Ni/Al.sub.2O.sub.3 or a combination of rhodium, iron, nickel, cobalt, molybdenum, iridium, palladium, platinum, or ruthenium.
19. The method of claim 12, wherein the catalyst reactor is heated using solar thermal power.
20. The method of claim 12, wherein the hydrocarbon end products are methane gas, methanol, ethanol, or syngas.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0008] For a more complete understanding of this disclosure, reference is now made to the following description, taken in conjunction with the accompanying drawings, in which:
[0009]
[0010]
DETAILED DESCRIPTION
[0011] Embodiments of the present disclosure may provide a direct air carbon capture catalyst system that may utilize different catalyst materials to produce hydrocarbons. The system may directly capture carbon dioxide from the air and purify it by passing the air through one or more membranes to separate and store air components. This also may get carbon dioxide ready for a chemical reaction to take place into the reactor that may be heated to a specified temperature based on the reactor core and type of hydrocarbon product. It should be appreciated that solar thermal heating may be used to heat the reactor without departing from the present disclosure. Catalyst materials may include, but are not limited to, metal composites and nanotech. Hydrocarbons produced may include, but are not limited to, methane and methanol. The system according to embodiments of the present disclosure may be scalable and modifiable. The resultant product may be scaled and may be transported easily, such as in a standard pickup truck. Further, the system according to embodiments of the present disclosure may use flood water to produce hydrogen needed for the reaction, as the system may be equipped with a water distiller.
[0012]
[0013] As depicted in
[0014]
[0015] As depicted in
[0016]
[0017] One or more solar panels may be used to capture sunlight and convert it into electricity to power the system in some embodiments of the present disclosure. In an embodiment of the present disclosure, six solar panels may be used; however, more or fewer may be used without departing from the present disclosure. The solar panels may be employed at a power of approximately 350 watts in an embodiment of the present disclosure. While solar panels are described herein, it should be appreciated that other forms of energy including, but not limited to, wind turbines, power directly from the grid, or power from a plant power generator, may be used without departing from the present disclosure. The generated electricity may then be used to generate methane gas through a series of processes involving the various components. The end result may be a clean and renewable hydrocarbon source that can be used for various applications.
[0018] Air or emissions are captured and pressurized by the compressor to the specifications needed to separate N.sub.2 and Argon gas from air through the membranes. The three-way valve and pressure gauges may work together to ensure that pressure needed to achieve the separation for each membrane is adequate. Flow meters may measure the flow rate of gases moving from the compressor to the membranes and needle valves installed before the membranes will allow for adjustment of the flow to achieve optimal separation. The shutoff valves may be placed as a precautionary safety mechanism to shutoff gas flow to the system in each step. Filters may be placed strategically to prevent the entry of unwanted components to the system's membranes.
[0019] Once the gas mixture moves through the separating process in the membranes, the N.sub.2 and Argon separated may be collected, and the O.sub.2 and CO.sub.2 mixture may move to the second separating stage. In this stage, porous polymers may be used to separate the O.sub.2 and CO.sub.2. Oxygen then may be collected, and the remaining CO.sub.2 may enter a reservoir tank. This tank may allow the system's flow adjustment at the reactors entrance in order to achieve the optimal mixture ratio at the injector. Simultaneously, the electrolysis cells may generate the needed H.sub.2. The flow of H.sub.2 gas may be adjusted and measured preparing gases to enter the injector where H.sub.2 and CO.sub.2 may be mixed and injected into the reactor. The catalyst's reactor chamber may heat to approximately 400 degrees Celsius to activate the catalyst's material and achieve maximum selectivity of CO.sub.2. In this stage, hydrogenation conversion of CO.sub.2 may produce methane gas. It should be appreciated that values identified herein are representative and should not be considered limiting with respect to the system and its applications. The components discussed herein are representative, and more or fewer components may be employed as applications require.
[0020] It should be appreciated that the conversion may be 1606 watts stored at 80% selectivity stored, and efficiency may be 75.6% at 80% selectivity in an embodiment of the present disclosure.
[0021] In some embodiments of the present disclosure, the carbon capture system may use chromatography techniques of separating gas molecules in a gas mixture for purposes of measurement and purification of feed gas or final product. These techniques may include, but are not limited to, the use of process gas chromatography and/or or the use of fused silica capillary columns, PLOT columns, Metal MTX capillary columns as well as packed and micro-packed columns, with properties ranging from either combination or stand-alone properties such as boiling point columns, polar, electronegative, molecular sieves, carbon blacks that are used with coding or with no coding of the solid base and puros polymers. These techniques may utilize vapor filtration columns, pressure gauges, flow meters, valves including diaphragm piston valves, and rotary valves that are spring-loaded or piston-less diaphragm valves, slide valves, and/or ball valves. There may be embodiments of the present disclosure that may use explosion-proof boxes or air-purged electronics as well as HMI for onsite control, and or inclusion of touch, or light sensitive sensors for input, Modbus, and serial and ethernet communication capabilities. Flame ionization detectors, thermal conductivity detectors, and flame photometric detectors may be used in the system in embodiments of the present disclosure. There also may be embodiments of the present disclosure that may use one or more of the following temperature probes and heating elements, automatic pressure regulators, manual pressure regulators, needle valves. hydrogen shut-off systems, solenoid valves, and/or compressed air and pressure sensors. It also should be appreciated that some separations may need cryogenic techniques.
[0022] The system according to embodiments of the present disclosure may utilize chemical reactions and clean power to produce valuable commodities. The system may capture carbon, lowering the need for drilling for natural gas. The system according to embodiments of the present disclosure may utilize the already built infrastructure of gas pipelines to ease the transition to clean power on the general population and the society.
[0023] In production plants and manufacturing sites and cities, the system according to embodiments of the present disclosure may capture carbon before it has a chance to move to higher altitudes where it can be more effective greenhouse gas than in lower altitudes. The system also may be installed on reservoirs to use flood water and reduce stress exerted on the reservoir's dam. It should be appreciated that the system according to embodiments of the present disclosure as well as the gases produced, such as oxygen and nitrogen, and hydrocarbons can be used in a variety of industries such as hospitals, chemical plants, plastic or ethylene plants and/or consumer items.
[0024] Although the present disclosure and its advantages have been described in detail, it should be understood that various changes, substitutions and alterations can be made herein without departing from the spirit and scope of the disclosure as defined by the appended claims. Moreover, the scope of the present application is not intended to be limited to the particular embodiments of the process, machine, manufacture, composition of matter, means, methods and steps described in the specification. As one of ordinary skill in the art will readily appreciate from the disclosure, processes, machines, manufacture, compositions of matter, means, methods, or steps, presently existing or later to be developed that perform substantially the same function or achieve substantially the same result as the corresponding embodiments described herein may be utilized according to the present disclosure. Accordingly, the appended claims are intended to include within their scope such processes, machines, manufacture, compositions of matter, means, methods, or steps.