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      Tuning sorbent properties to reduce the cost of direct air capture

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          Abstract

          A direct air capture (DAC) economic model that accounts for sorbent degradation is developed. Experimentally-measured parameters are then integrated to identify sorbent and process features that minimize both the DAC carbon footprint and cost.

          Abstract

          The question has shifted from whether solid sorbents can work in direct air capture (DAC) technologies to which solid sorbents are more economically advantaged. Determining this is challenging due to the influence of many different yet interconnected sorbent properties on the cost of CO 2 capture. Existing DAC economic models oversimplify sorbent stability by treating it as a simple replacement rate, neglecting crucial factors such as capacity loss rate and form. To address this challenge, we have developed an economic model that accounts for sorbent degradation in DAC processes. By factoring in capacity loss over time, our model provides a more accurate estimate of the cost associated with DAC and highlights the optimum time for sorbent replacement. We then identified sorbent characteristics and process features that minimize both the carbon footprint and the cost of captured CO 2. To further investigate the interplay of sorbent properties and DAC cost, we constructed a series of alkyl- and epoxy-functionalized polyamine sorbents. The sorbents’ CO 2 uptake, heat of adsorption and capacity fade were adjusted via a one-step modification, varying the proportions of primary, secondary, and tertiary amines. We then integrated the experimentally-measured parameters, including the form of degradation, into our economic model to probe which combination of sorbent properties results in the lowest cost of DAC for a fixed operating condition. The results provide guidelines and priorities for sorbent performance metrics that will yield the most cost-effective DAC technologies.

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          Irreversible climate change due to carbon dioxide emissions.

          The severity of damaging human-induced climate change depends not only on the magnitude of the change but also on the potential for irreversibility. This paper shows that the climate change that takes place due to increases in carbon dioxide concentration is largely irreversible for 1,000 years after emissions stop. Following cessation of emissions, removal of atmospheric carbon dioxide decreases radiative forcing, but is largely compensated by slower loss of heat to the ocean, so that atmospheric temperatures do not drop significantly for at least 1,000 years. Among illustrative irreversible impacts that should be expected if atmospheric carbon dioxide concentrations increase from current levels near 385 parts per million by volume (ppmv) to a peak of 450-600 ppmv over the coming century are irreversible dry-season rainfall reductions in several regions comparable to those of the "dust bowl" era and inexorable sea level rise. Thermal expansion of the warming ocean provides a conservative lower limit to irreversible global average sea level rise of at least 0.4-1.0 m if 21st century CO(2) concentrations exceed 600 ppmv and 0.6-1.9 m for peak CO(2) concentrations exceeding approximately 1,000 ppmv. Additional contributions from glaciers and ice sheet contributions to future sea level rise are uncertain but may equal or exceed several meters over the next millennium or longer.
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            Carbon capture and storage (CCS): the way forward

            Carbon capture and storage (CCS) is vital to climate change mitigation, and has application across the economy, in addition to facilitating atmospheric carbon dioxide removal resulting in emissions offsets and net negative emissions. This contribution reviews the state-of-the-art and identifies key challenges which must be overcome in order to pave the way for its large-scale deployment. Carbon capture and storage (CCS) is broadly recognised as having the potential to play a key role in meeting climate change targets, delivering low carbon heat and power, decarbonising industry and, more recently, its ability to facilitate the net removal of CO 2 from the atmosphere. However, despite this broad consensus and its technical maturity, CCS has not yet been deployed on a scale commensurate with the ambitions articulated a decade ago. Thus, in this paper we review the current state-of-the-art of CO 2 capture, transport, utilisation and storage from a multi-scale perspective, moving from the global to molecular scales. In light of the COP21 commitments to limit warming to less than 2 °C, we extend the remit of this study to include the key negative emissions technologies (NETs) of bioenergy with CCS (BECCS), and direct air capture (DAC). Cognisant of the non-technical barriers to deploying CCS, we reflect on recent experience from the UK's CCS commercialisation programme and consider the commercial and political barriers to the large-scale deployment of CCS. In all areas, we focus on identifying and clearly articulating the key research challenges that could usefully be addressed in the coming decade.
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              Adsorbent materials for carbon dioxide capture from large anthropogenic point sources.

              Since the time of the industrial revolution, the atmospheric CO(2) concentration has risen by nearly 35 % to its current level of 383 ppm. The increased carbon dioxide concentration in the atmosphere has been suggested to be a leading contributor to global climate change. To slow the increase, reductions in anthropogenic CO(2) emissions are necessary. Large emission point sources, such as fossil-fuel-based power generation facilities, are the first targets for these reductions. A benchmark, mature technology for the separation of dilute CO(2) from gas streams is via absorption with aqueous amines. However, the use of solid adsorbents is now being widely considered as an alternative, potentially less-energy-intensive separation technology. This Review describes the CO(2) adsorption behavior of several different classes of solid carbon dioxide adsorbents, including zeolites, activated carbons, calcium oxides, hydrotalcites, organic-inorganic hybrids, and metal-organic frameworks. These adsorbents are evaluated in terms of their equilibrium CO(2) capacities as well as other important parameters such as adsorption-desorption kinetics, operating windows, stability, and regenerability. The scope of currently available CO(2) adsorbents and their critical properties that will ultimately affect their incorporation into large-scale separation processes is presented.
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                Author and article information

                Contributors
                (View ORCID Profile)
                (View ORCID Profile)
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                Journal
                EESNBY
                Energy & Environmental Science
                Energy Environ. Sci.
                Royal Society of Chemistry (RSC)
                1754-5692
                1754-5706
                July 02 2024
                2024
                : 17
                : 13
                : 4544-4559
                Affiliations
                [1 ]School of Chemical & Biomolecular Engineering, Georgia Institute of Technology, 311 Ferst Drive, Atlanta, Georgia 30332, USA
                Article
                10.1039/D4EE00616J
                4f9c8370-44eb-45b2-aefb-efac36a685d6
                © 2024

                http://creativecommons.org/licenses/by/3.0/

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