Sunho Choi

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.

Amine‐Tethered Solid Adsorbents Coupling High Adsorption Capacity and Regenerability for CO2 Capture From Ambient Air

Silica supported poly(ethyleneimine) (PEI) materials are prepared via impregnation and demonstrated to be promising adsorbents for CO(2) capture from ultra-dilute gas streams such as ambient air. A prototypical class 1 adsorbent, containing 45 wt% PEI (PEI/silica), and two new modified PEI-based aminosilica adsorbents, derived from PEI modified with 3-aminopropyltrimethoxysilane (A-PEI/silica) or tetraethyl orthotitanate (T-PEI/silica), are prepared and characterized by using thermogravimetric analysis and FTIR spectroscopy. The modifiers are shown to enhance the thermal stability of the polymer-oxide composites, leading to higher PEI decomposition temperatures. The modified adsorbents present extremely high CO(2) adsorption capacities under conditions simulating ambient air (400 ppm CO(2) in inert gas), exceeding 2 mol(CO (2)) kg(sorbent)(-1), as well as enhanced adsorption kinetics compared to conventional class 1 sorbents. The new adsorbents show excellent stability in cyclic adsorption-desorption operations, even under dry conditions in which aminosilica adsorbents are known to lose capacity due to urea formation. Thus, the adsorbents of this type can be considered promising materials for the direct capture of CO(2) from ultra-dilute gas streams such as ambient air.

Modification of the Mg/DOBDC MOF with Amines to Enhance CO2 Adsorption from Ultradilute Gases

The MOF Mg/DOBDC has one of the highest known CO2 adsorption capacities at the low to moderate CO2 partial pressures relevant for CO2 capture from flue gas but is difficult to regenerate for use in cyclic operation. In this work, Mg/DOBDC is modified by functionalization of its open metal coordination sites with ethylene diamine (ED) to introduce pendent amines into the MOF micropores. DFT calculations and experimental nitrogen physisorption and thermogravimetric analysis suggest that 1 ED molecule is added to each unit cell, on average. This modification both increases the materials CO2 adsorption capacity at ultradilute CO2 partial pressures and increases the regenerability of the material, allowing for cyclic adsorption-desorption cycles with identical adsorption capacities. This is one of the first MOF materials demonstrated to yield significant adsorption capacities from simulated ambient air (400 ppm CO2), and its capacity is competitive with the best-known adsorbents based on amine-oxide composites.

Structural changes of silica mesocellular foam supported amine-functionalized CO2 adsorbents upon exposure to steam

Three classes of amine-functionalized mesocellular foam (MCF) materials are prepared and evaluated as CO(2) adsorbents. The stability of the adsorbents under steam/air and steam/nitrogen conditions is investigated using a Parr autoclave reactor to simulate, in an accelerated manner, the exposure that such adsorbents will see under steam stripping regeneration conditions at various temperatures. The CO(2) capacity and organic content of all adsorbents decrease after steam treatment under both steam/air and steam/nitrogen conditions, primarily due to structural collapse of the MCF framework, but with additional contributions likely associated with amine degradation during treatment under harsh conditions. Treatment with steam/air is found to have stronger effect on the CO(2) capacity of the adsorbents compared to steam/nitrogen.

Effect of Pore Structure on CO2 Adsorption Characteristics of Aminopolymer Impregnated MCM-36

The CO2 adsorption characteristics of a pillared 2-dimensional porous silicate material impregnated with amine containing polymers have been investigated. It was determined that the introduction of amine polymer deteriorates the CO2 capture kinetics of the MCM-36 supported amine adsorbents compared to that of the bare material, due to the fact that with the addition of a higher loading of amine polymer the diffusion of CO2 through the 2-dimensional interlayer mesoporous channels of MCM-36 becomes greatly hindered. This pore blocking sets an upper limit to the CO2 capture performance of the polymer impregnated MCM-36 and greatly reduces the utility of using this sort of amine-solid adsorbent for carbon capture. Interestingly, these results suggest that for 2-D channel solid supports there is an optimal amine loading which is not likely to be equal to the maximum loading, and which can be determined and utilized to obtain the maximum improvement over the original materials. The study performed in this work for the MCM-36 material could therefore be applied to other porous supports to determine these optimum loadings and be used to more easily compare and contrast the alterations to capture characteristics which occur upon amine loading for a wide range of materials. It is believed this will make it more straightforward to determine which solid supports hold the promise for greatly improved capture characteristics upon amine loading and allow the field to more quickly determine avenues for fruitful development. These results also suggest the need for a new sort of support structure for amine loaded solids, one which can allow us to decouple amine loading from increasing diffusion resistance so that high amine efficiency can be maintained throughout the range of increased amine loadings.

Functionalization of Metal–Organic Frameworks for Enhanced Stability under Humid Carbon Dioxide Capture Conditions

Metal-organic frameworks (MOFs) have been highlighted recently as promising materials for CO2 capture. However, in practical CO2 capture processes, such as capture from flue gas or ambient air, the adsorption properties of MOFs tend to be harmed by the presence of moisture possibly because of the hydrophilic nature of the coordinatively unsaturated sites (CUSs) within their framework. In this work, the CUSs of the MOF framework are functionalized with amine-containing molecules to prevent structural degradation in a humid environment. Specifically, the framework of the magnesium dioxybenzenedicarboxylate (Mg/DOBDC) MOF was functionalized with ethylenediamine (ED) molecules to make the overall structure less hydrophilic. Structural analysis after exposure to high-temperature steam showed that the ED-functionalized Mg/DOBDC (ED-Mg/DOBDC) is more stable under humid conditions, than Mg/DOBDC, which underwent drastic structural changes. ED-Mg/DOBDC recovered its CO2 adsorption capacity and initial adsorption rate quite well as opposed to the original Mg/DOBDC, which revealed a significant reduction in its capture capacity and kinetics. These results suggest that the amine-functionalization of the CUSs is an effective way to enhance the structural stability of MOFs as well as their capture of humid CO2 .

Swelling, Functionalization, and Structural Changes of the Nanoporous Layered Silicates AMH-3 and MCM-22

Nanoporous layered silicate materials contain 2D-planar sheets of nanoscopic thickness and ordered porous structure. In comparison to porous 3D-framework materials such as zeolites, they have advantages such as significantly increased surface area and decreased diffusion limitations because the layers can potentially be exfoliated or intercalated into polymers to form nanocomposite materials. These properties are particularly interesting for applications as materials for enhancing molecular selectivity and throughput in composite membranes. In this report, the swelling and surface modification chemistry of two attractive nanoporous layered silicate materials, AMH-3 and MCM-22, were studied. We first describe a method, using long-chain diamines instead of monoamines, for swelling of AMH-3 while preserving its pore structure to a greater extent during the swelling process. Then, we describe a stepwise functionalization method for functionalizing the layer surfaces of AMH-3 and MCM-22 via silane condensation reactions. The covalently attached hydrocarbon chain molecules increased the hydrophobicity of AMH-3 and MCM-22 layer surfaces and therefore allow the possibility of effectively dispersing these materials in polymer matrices for thin film/membrane applications.

Pore structure–CO2 adsorption property relations of supported amine materials with multi-pore networks

Conventional supported amine adsorbents to date are known to suffer from the trade-off between increasing amine content and decreasing access to amine sites. In this work, we propose a solution to this known issue by introducing substrates with multiple pore networks where each pore channel can be used for amine loading and gas diffusion. It was hypothesized that these types of substrates with a multi-pore system would allow for a high amine content without a decrease in diffusion speed or amine efficiency. As a proof of concept, a 3-dimensional silica mesoporous framework composed of agglomerated spheres of microporous zeolite beta was loaded with large or small amine-containing molecules. The resulting hybrid adsorbents include mesopores loaded with large amine molecules or micropores incorporating small amine molecules, where molecular recognition using different pore dimensions allows selective incorporation of amine groups according to their molecular size. As a result of this selective amine loading, the supported amine adsorbent system proposed here demonstrates fast sorption kinetics at all amine loadings while maintaining amine efficiencies near the theoretical maximum value, which has not been achieved in supported amine adsorbents of this class as yet. Thus, this work may unlock new opportunities for the study of solid amine adsorbents with high efficiency amine utilization and fast achievement of near equilibrium capacities.