0
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Cold Temperature Direct Air CO 2 Capture with Amine-Loaded Metal–Organic Framework Monoliths

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Zeolites, silica-supported amines, and metal–organic frameworks (MOFs) have been demonstrated as promising adsorbents for direct air CO 2 capture (DAC), but the shaping and structuring of these materials into sorbent modules for practical processes have been inadequately investigated compared to the extensive research on powder materials. Furthermore, there have been relatively few studies reporting the DAC performance of sorbent contactors under cold, subambient conditions (temperatures below 20 °C). In this work, we demonstrate the successful fabrication of adsorbent monoliths composed of cellulose acetate (CA) and adsorbent particles such as zeolite 13X and MOF MIL-101(Cr) by a 3D printing technique: solution-based additive manufacturing (SBAM). These monoliths feature interpenetrated macroporous polymeric frameworks in which microcrystals of zeolite 13X or MIL-101(Cr) are evenly distributed, highlighting the versatility of SBAM in fabricating monoliths containing sorbents with different particle sizes and density. Branched poly(ethylenimine) (PEI) is successfully loaded into the CA/MIL-101(Cr) monoliths to impart CO 2 uptakes of 1.05 mmol g monolith –1 at −20 °C and 400 ppm of CO 2. Kinetic analysis shows that the CO 2 sorption kinetics of PEI-loaded MIL-101(Cr) sorbents are not compromised in the monoliths compared to the powder sorbents. Importantly, these monoliths exhibit promising working capacities (0.95 mmol g monolith –1) over 14 temperature swing cycles with a moderate regeneration temperature of 60 °C. Dynamic breakthrough experiments at 25 °C under dry conditions reveal a CO 2 uptake capacity of 0.60 mmol g monolith –1, which further increases to 1.05 and 1.43 mmol g monolith –1 at −20 °C under dry and humid (70% relative humidity) conditions, respectively. Our work showcases the successful implementation of SBAM in making DAC sorbent monoliths with notable CO 2 capture performance over a wide range of sorption temperatures, suggesting that SBAM can enable the preparation of efficient sorbent contactors in various form factors for other important chemical separations.

          Related collections

          Most cited references51

          • Record: found
          • Abstract: found
          • Article: not found

          Direct Capture of CO2 from Ambient Air.

          The increase in the global atmospheric CO2 concentration resulting from over a century of combustion of fossil fuels has been associated with significant global climate change. With the global population increase driving continued increases in fossil fuel use, humanity's primary reliance on fossil energy for the next several decades is assured. Traditional modes of carbon capture such as precombustion and postcombustion CO2 capture from large point sources can help slow the rate of increase of the atmospheric CO2 concentration, but only the direct removal of CO2 from the air, or "direct air capture" (DAC), can actually reduce the global atmospheric CO2 concentration. The past decade has seen a steep rise in the use of chemical sorbents that are cycled through sorption and desorption cycles for CO2 removal from ultradilute gases such as air. This Review provides a historical overview of the field of DAC, along with an exhaustive description of the use of chemical sorbents targeted at this application. Solvents and solid sorbents that interact strongly with CO2 are described, including basic solvents, supported amine and ammonium materials, and metal-organic frameworks (MOFs), as the primary classes of chemical sorbents. Hypothetical processes for the deployment of such sorbents are discussed, as well as the limited array of technoeconomic analyses published on DAC. Overall, it is concluded that there are many new materials that could play a role in emerging DAC technologies. However, these materials need to be further investigated and developed with a practical sorbent-air contacting process in mind if society is to make rapid progress in deploying DAC as a means of mitigating climate change.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Immobilizing highly catalytically active Pt nanoparticles inside the pores of metal-organic framework: a double solvents approach.

            Ultrafine Pt nanoparticles were successfully immobilized inside the pores of a metal-organic framework, MIL-101, without aggregation of Pt nanoparticles on the external surfaces of framework by using a "double solvents" method. TEM and electron tomographic measurements clearly demonstrated the uniform three-dimensional distribution of the ultrafine Pt NPs throughout the interior cavities of MIL-101. The resulting Pt@MIL-101 composites represent the first highly active MOF-immobilized metal nanocatalysts for catalytic reactions in all three phases: liquid-phase ammonia borane hydrolysis, solid-phase ammonia borane thermal dehydrogenation, and gas-phase CO oxidation.
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              Direct Air Capture of CO2 Using Amine Functionalized MIL-101(Cr)

                Bookmark

                Author and article information

                Journal
                ACS Appl Mater Interfaces
                ACS Appl Mater Interfaces
                am
                aamick
                ACS Applied Materials & Interfaces
                American Chemical Society
                1944-8244
                1944-8252
                18 December 2023
                10 January 2024
                : 16
                : 1
                : 1404-1415
                Affiliations
                School of Chemical & Biomolecular Engineering, Georgia Institute of Technology , 311 Ferst Dr., Atlanta, Georgia 30332, United States
                Author notes
                Author information
                https://orcid.org/0000-0002-6945-6431
                https://orcid.org/0000-0001-8244-8308
                https://orcid.org/0000-0002-3199-1711
                https://orcid.org/0000-0003-3255-5791
                https://orcid.org/0000-0002-8039-4008
                Article
                10.1021/acsami.3c13528
                10788822
                38109480
                db3ed9e7-ed98-4ae6-ae28-45e6d63ebb42
                © 2023 The Authors. Published by American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 10 September 2023
                : 29 November 2023
                : 29 November 2023
                Funding
                Funded by: Division of Electrical, Communications and Cyber Systems, doi 10.13039/100000148;
                Award ID: ECCS-2025462
                Funded by: Zero Carbon Partners, LLC, doi NA;
                Award ID: NA
                Funded by: Georgia Tech Institute for Electronics and Nanotechnology, doi NA;
                Award ID: NA
                Funded by: National Energy Technology Laboratory, doi 10.13039/100013165;
                Award ID: DE-FE-FE0031952
                Categories
                Research Article
                Custom metadata
                am3c13528
                am3c13528

                Materials technology
                3d printing,carbon capture,direct air capture,metal−organic frameworks,subambient conditions

                Comments

                Comment on this article