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Carbon capture from large sources and ambient air is one of the most promising strategies to curb the deleterious effect of greenhouse gases. Among different technologies, CO2 adsorption has drawn widespread attention mostly because of its low energy requirements. Considering that water vapor is a ubiquitous component in air and almost all CO2-rich industrial gas streams, understanding its impact on CO2 adsorption is of critical importance. Owing to the large diversity of adsorbents, water plays many different roles from a severe inhibitor of CO2 adsorption to an excellent promoter. Water may also increase the rate of CO2 capture or have the opposite effect. In the presence of amine-containing adsorbents, water is even necessary for their long-term stability. The current contribution is a comprehensive review of the effects of water whether in the gas feed or as adsorbent moisture on CO2 adsorption. For convenience, we discuss the effect of water vapor on CO2 adsorption over four broadly defined groups of materials separately, namely (i) physical adsorbents, including carbons, zeolites and MOFs, (ii) amine-functionalized adsorbents, and (iii) reactive adsorbents, including metal carbonates and oxides. For each category, the effects of humidity level on CO2 uptake, selectivity, and adsorption kinetics under different operational conditions are discussed. Whenever possible, findings from different sources are compared, paying particular attention to both similarities and inconsistencies. For completeness, the effect of water on membrane CO2 separation is also discussed, albeit briefly.

The accumulation of non-desorbed species or heel buildup reduces the capacity and lifetime of adsorbents used in cyclic adsorption/desorption processes. This study investigates the changes in the physical, chemical, and dielectric properties of beaded activated carbon (BAC) and their relation to the adsorbent residual capacity (i.e., residual lifetime) during cyclic adsorption/desorption using a non-contact, high-resolution microwave resonator sensor. The resonant frequency of the sensor responds to changes in the dielectric properties of the medium surrounding the sensor. BAC samples with different degrees of capacity reduction as indicated by the apparent density, BET surface area, total pore and micropore volumes were tested. A linear correlation (R2 = 0.93) between the apparent density of the BAC samples and the resonant frequency shift of the sensor was observed, irrespective of heel composition indicating that the effect of adsorbent porosity on dielectric property variation is more important than heel composition. The sensor’s ability for fast and continuous measurement makes it an ideal candidate for real-time monitoring of adsorbent capacity status in cyclic adsorption/desorption processes.

This study investigates the hydrothermal stability of triamine-grafted CO2 adsorbent based on a commercial-grade silica (CARiACT, P10). Grafting was conducted in dry and wet conditions at 85 °C. At optimum grafting conditions using 0.2 cm3 water and 1.5 cm3 aminosilane per gram of silica, the highest CO2 uptake of 1.93 mmol/g at 50 °C was obtained. This material was exposed to steam at 120 °C for up to 360 h. It was observed that increasing the duration of steam exposure from 3 to 24 h reduced adsorption uptake at 25 °C by 56%. However, the CO2 uptake reduction was much less severe at higher adsorption temperatures, reaching 21% at 50 °C and only 4% at 75 °C. Conducting steam treatment for 360 h reduced adsorption uptake at 25, 50, and 75 °C by 83, 61, and 26%, respectively. For this extreme steaming experiment, the decrease in CO2 uptake at all adsorption temperatures was attributed to the reduction of the sorbent average pore width, increasing diffusional mass transfer resistance. The results revealed t...

A two-dimensional heterogeneous computational fluid dynamics model was developed and validated to study the mass, heat, and momentum transport in a fixed-bed cylindrical adsorber during the adsorption of volatile organic compounds (VOCs) from a gas stream onto a fixed bed of beaded activated carbon (BAC). Experimental validation tests revealed that the model predicted the breakthrough curves for the studied VOCs (acetone, benzene, toluene, and 1,2,4-trimethylbenzene) as well as the pressure drop and temperature during benzene adsorption with a mean relative absolute error of 2.6, 11.8, and 0.8%, respectively. Effects of varying adsorption process variables such as carrier gas temperature, superficial velocity, VOC loading, particle size, and channelling were investigated. The results obtained from this study are encouraging because they show that the model was able to accurately simulate the transport processes in an adsorber and can potentially be used for enhancing absorber design and operation.

A newly developed noncontact high-resolution real-time microwave sensor was used to determine the breakthrough time and adsorption capacity of adsorbents/adsorbates with different dielectric properties. The sensor is a microwave microstrip planar resonator with an enhanced quality factor using a regenerative feedback loop operating at 1.4 GHz and an adjustable quality factor of 200-200000. Beaded activated carbon (BAC, microwave-absorbing) and a polymeric adsorbent (V503, microwave transparent) were completely loaded with 1,2,4-trimethylbenzene (nonpolar) or 2-butoxyethanol (polar). During adsorption, variations in the dielectric properties of the adsorbents were monitored using two microwave parameters; quality factor and resonant frequency. Those parameters were related to adsorption breakthrough time and capacity. Adsorption tests were completed at select relative pressures (0.03, 0.1, 0.2, 0.4, and 0.6) of adsorbates in the influent stream. For all experiments, the difference between the breakthrough time (t5%) and the settling time of the quality factor variation (time that the quality factor was 0.95 of its final value) was

Incomplete regeneration of activated carbon loaded with organic compounds results in heel build-up that reduces the useful life of the adsorbent. In this study, microwave heating was tested as a regeneration method for beaded activated carbon (BAC) loaded with n-dodecane, a high molecular weight volatile organic compound. Energy consumption and desorption efficiency for microwave-heating regeneration were compared with conductive-heating regeneration. The minimum energy needed to completely regenerate the adsorbent (100% desorption efficiency) using microwave regeneration was 6% of that needed with conductive heating regeneration, owing to more rapid heating rates and lower heat loss. Analyses of adsorbent pore size distribution and surface chemistry confirmed that neither heating method altered the physical/chemical properties of the BAC. Additionally, gas chromatography (with flame ionization detector) confirmed that neither regeneration method detectably altered the adsorbate composition during desorption. By demonstrating improvements in energy consumption and desorption efficiency and showing stable adsorbate and adsorbent properties, this paper suggests that microwave heating is an attractive method for activated carbon regeneration particularly when high-affinity VOC adsorbates are present.

This paper investigates the effect of the kinetic diameter (KD) of the reference adsorbate on the accuracy of the Dubinin-Radushkevich (D-R) equation for predicting the adsorption isotherms of organic vapors on microporous activated carbon. Adsorption isotherms for 13 organic compounds on microporous beaded activated carbon were experimentally measured, and predicted using the D-R model and affinity coefficients. The affinity coefficients calculated based on molar volumes, molecular polarizabilities, and molecular parachors were used to predict the isotherms based on four reference compounds (4.3≤KD≤6.8 A). The results show that the affinity coefficients are independent of the calculation method if the reference and test adsorbates are from the same organic group. Choosing a reference adsorbate with a KD similar to that of the test adsorbate results in better prediction of the adsorption isotherm. The relative error between the predicted and the measured adsorption isotherms increases as the absolute difference in the kinetic diameters of the reference and test adsorbates increases. Finally, the proposed hypothesis was used to explain reports of inconsistent findings among published articles. The results from this study are important because they allow a more accurate prediction of adsorption capacities of adsorbents which allow for better design of adsorption systems.

In this study, adsorption and desorption of mixtures of organic compounds commonly emitted from automotive painting operations were experimentally studied. A mixture of two alkanes and a mixture of eight organic compounds were adsorbed onto beaded activated carbon (BAC) and then thermally desorbed under nitrogen. Following both adsorption and regeneration, samples of the BAC were chemically extracted. Gas chromatography-mass spectrometry (GC-MS) was used to quantify the compounds in the adsorption and desorption gas streams and in the BAC extracts. In general, for both adsorbate mixtures, competitive adsorption resulted in displacing low boiling point compounds by high boiling point compounds during adsorption. In addition to boiling point, adsorbate structure and functionality affected adsorption dynamics. High boiling point compounds such as n-decane and 2,2-dimethylpropylbenzene were not completely desorbed after three hours regeneration at 288 °C indicating that these two compounds contributed to heel accumulation on the BAC. Additional compounds not present in the mixtures were detected in the extract of regenerated BAC possibly due to decomposition or other reactions during regeneration. Closure analysis based on breakthrough curves, solvent extraction of BAC and mass balance on the reactor provided consistent results of the amount of adsorbates on the BAC after adsorption and/or regeneration.

This paper investigates the effect of adsorption and regeneration temperature on the irreversible adsorption of a mixture of organic compounds typically emitted from automobile painting operations. Adsorption of the organic vapors mixture onto microporous beaded activated carbon (BAC) and regeneration of the saturated BAC were completed under different conditions. Results indicated that increasing the adsorption temperature from 25 to 35 or 45 °C increased heel buildup on BAC by about 30% irrespective of the regeneration temperature due to chemisorption. The adsorption capacity (for the first cycle) of the mixture onto the BAC at these three temperatures remained almost unchanged indicating chemisorption of some of these compounds onto the BAC. Increasing the regeneration temperature from 288 to 400 °C resulted in 61% reduction in the heel at all adsorption temperatures, possibly due to desorption of chemicals from narrow micropores. BET area and pore volumes of the BAC decreased proportionally to the cumulative heel. Pore size distribution and pore volume reduction confirmed that the heel was mainly built up in narrow micropores which can be occupied or blocked by some of the adsorbates.

A microbead-assisted planar microwave resonator for organic vapor sensing applications is presented. The core of this sensor is a planar microstrip split-ring resonator, integrated with an active feedback loop to enhance the initial quality factor from 200 to ∼1 M at an operational resonance frequency of 1.42 GHz. Two different types of microbeads, beaded activated carbon (BAC) and polymer based (V503) beads, are investigated in non-contact mode for use as gas adsorbents in the gas sensing device. 2-Butoxyethanol (BE) is used in various concentrations as the target gas, and the transmitted power (S21) of the two port resonator is measured. The two main microwave parameters of resonance frequency and quality factor are extracted from S21 since these parameters are less susceptible to environmental and instrumental noise than the amplitude. Measured results demonstrate a minimum resonance frequency shift of 10 kHz for a 35 ppm concentration of BE exposure to carbon beads and 160 kHz for the polymer based adsorbent at the same concentration. The quality factor of the resonator also changed for different concentrations, but a distinguishable variation is observed for the BAC adsorbents. The high quality factor of the sensor provides the opportunity of real time monitoring of the adsorbent behaviors in remote sensing mode with very high resolution.