The present disclosure relates generally to the field of component extraction or collection from gases. More particularly, this disclosure relates to methods and systems for direct air capture of carbon dioxide (CO2) to reduce CO2 emissions and atmospheric water harvesting to enhance water availability.
According to a recent report published by the Intergovernmental Panel on Climate Change of the United Nations, efforts to reduce global warming will miss the goals of the Paris Agreement unless deep reductions in carbon dioxide (CO2) emissions occur in the coming decades. While carbon capture is among the most effective approaches to reducing CO2 emissions, the high cost is one of the largest barriers for existing carbon capture technologies to be widely adopted. Existing solutions often aim at improving some direct air capture (DAC) metrics while compromising others. As a result, the cost reduction from such improvements is small.
Sorbent-based DAC has been proposed for CO2 capture techniques. However, current proposals have yet to solve the challenging and complex problems posed by such approaches to maximize the CO2 capture efficiency. As a result, conventional DAC technologies to reduce CO2 are not cost effective for industry adoption. Thus, a need remains for improved techniques to optimize sorbents for DAC to collect CO2 in a more efficient and cost-effective manner.
According to an aspect of the invention, a system for extracting components from a gas includes an inlet configured to accept a gas; at least one chamber configured to collect water from the gas accepted via the inlet; at least one chamber configured to collect carbon dioxide from the gas accepted via the inlet; wherein the at least one chamber configured to collect water and the at least one chamber configured to collect carbon dioxide each comprise a topologically optimized sorbent with hierarchical pores; and wherein the at least one chamber configured to collect water and the at least one chamber configured to collect carbon dioxide are each configured to respectively release the collected water and the collected carbon dioxide.
According to another aspect of the invention, a method for extracting components from a gas includes accepting a gas via an inlet; collecting water from the accepted gas in at least one chamber configured to collect water; collecting carbon dioxide from the accepted gas in at least one chamber configured to collect carbon dioxide; wherein the at least one chamber configured to collect water and the at least one chamber configured to collect carbon dioxide each comprise a topologically optimized sorbent with hierarchical pores; and wherein the at least one chamber configured to collect water and the at least one chamber configured to collect carbon dioxide are each configured to respectively release the collected water and the collected carbon dioxide.
According to another aspect of the invention, a system for extracting components from a gas includes an inlet configured to accept a gas; at least one chamber configured to collect water from the gas accepted via the inlet; at least one chamber configured to collect carbon dioxide from the gas accepted via the inlet; wherein the at least one chamber configured to collect water and the at least one chamber configured to collect carbon dioxide each comprise a topologically optimized sorbent with hierarchical pores; and wherein the at least one chamber configured to collect water and the at least one chamber configured to collect carbon dioxide are each configured to cycle between a sorption mode and a desorption mode.
The following figures form part of the present specification and are included to further demonstrate certain aspects of the present disclosure and should not be used to limit the claimed subject matter. The figures are not necessarily drawn to scale, and certain features may be shown exaggerated in scale or in generalized or schematic form, in the interest of clarity and conciseness.
The disclosed subject matter may be better understood by reference to one or more of the drawings in combination with the description of embodiments disclosed herein. Consequently, a more complete understanding of the present embodiments and further features and advantages thereof may be acquired by referring to the following description taken in conjunction with the accompanying drawings, in which like reference numerals may identify like elements. It should be understood, however, that the embodiments are not limited to the precise arrangements and configurations shown in the figures.
This disclosure presents innovative monolithic sorbents that have a hierarchical and interconnected pore structure, reducing the energy needed for CO2 adsorption and desorption. Disclosed herein are topologically optimized sorbent embodiments with multiscale cavities. As used herein, the terms “sorbent” and “adsorbent” are used interchangeably. The disclosed sorbent embodiments are produced via a novel technique using binder jetting additive manufacturing (3D printing) with granulated powder.
The produced sorbent 110 has interconnected pores at four different scales P1, P2, P3, P4. The quadrimodal pore size distribution of the monolithic sorbent 110 embodiments is realized through different mechanisms. First, designed pores P1 on the order of 100 μm or larger are enabled by the geometric flexibility of binder jetting additive manufacturing. The shape and size of these macropores can be directly specified through computer-aided design. Second, intergranular pores P2 on the order of 10 μm are introduced by using granulated powder as the feedstock powder. Third, interparticle pores P3 on the order of 1 μm are formed between the Zeolite particles. Lastly, each Zeolite particle, as a molecular sieve, contains intraparticle pores P4 on the order of 1 nm. In some embodiments, the feedstock powder for binder jetting additive manufacturing is made of 13X Zeolite powder. This material is selected because of its demonstrated performance for CO2 adsorption. The Zeolite powder (Product No. 283592, Sigma-Aldrich) has an average particle size of 2 μm.
The feedstock powder for implementation of the disclosed embodiments may be prepared in more than one way.
In some embodiments, the feedstock powder preparation parameters may be optimized by adding a dispersant (e.g. Dolapix PC 75) to the slurry 20 to reduce the viscosity for spraying. The weight ratio of the dispersant to the solid (Zeolite powder) can be tuned from 0.3% to 0.2%, 0.1%, and 0%. The smallest amount of the dispersant for successful spraying may be selected because of the lowest possibility for blocking the pores in the Zeolite. The feed rate and spraying pressure in the spray freezing step may be tuned to achieve the maximum yield. Results from testing showed that the granule size increases with increasing feed rate and decreasing spraying pressure.
Conventional binder jetting 3D printers may be used to implement embodiments of this disclosure (e.g., ExOne Innovent+). The working principle of the 3D printers is shown in
Once the topologically optimized sorbents 110 are produced as described herein, they can be integrated into a DAC application.
In the depicted system 300, line 4B is shut off from receiving ambient air via the inlet 40 since another chamber 56 configured with the topologically optimized sorbents 110 to collect H2O was previously filled. The filled chamber 56 is heated with a heat source 58 to instigate the release of water from the sorbents 110, which is then channeled via valve 60 for storage in an H2O tank 62.
In some embodiments, a pump 64 is linked to the H2O tank to facilitate filling and/or emptying of the tank. Line 4B is also configured with a pre-filled chamber 66 configured with the topologically optimized sorbents 110 to collect CO2. This chamber 66 is also heated with a heat source 68 to instigate the release of CO2 from the sorbents 110, which is then channeled via valve 70 for storage in a CO2 tank 72. In some embodiments, a pump 74 is linked to the CO2 tank to facilitate filling and/or emptying of the tank. In this manner, line 4B is operating in an H2O desorption mode and CO2 desorption mode.
Advantages of the disclosed sorbents 110 and techniques include a reduction in cost compared to conventional CO2 capture technologies. The topological optimization of sorbents 110 can be engineered to produce the desired multiscale cavities and pore structures. The sorbents 110 can be recycled between sorption-desorption cycles for many iterations. The embodiments may be implemented for scalable DAC and location-independent operations. The disclosed embodiments also avoid thermal and chemical degradation, evaporation, and corrosion issues seen in conventional liquid solvent capture technologies. The sorbents 110 also avoid particle attrition seen in conventional pellet-based solid sorbent capture technologies. The disclosed embodiments also save space (enabled by the increased volumetric adsorption capacity).
It will be appreciated by those skilled in the art that the disclosed embodiments may be implemented using conventional hardware, components, materials, and software and computer systems programmed to perform the disclosed processes and operations. In light of the principles and example embodiments described and illustrated herein, it will be recognized that the example embodiments can be modified in arrangement and detail without departing from such principles. It will also be appreciated that embodiments of this disclosure may be implemented for use with any gas in any environment. In view of the wide variety of useful permutations that may be readily derived from the example embodiments described herein, this detailed description is intended to be illustrative only, and should not be taken as limiting the scope of the invention.
This application claims priority to U.S. Provisional Patent Application No. 63/545,552 filed on Oct. 25, 2023. The entire disclosure of Application No. 63/545,552 is hereby incorporated herein by reference.
Number | Date | Country | |
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63545552 | Oct 2023 | US |