Utilization of Deep Eutectic Solvents to Reduce the Release of Hazardous Gases to the Atmosphere: A Critical Review

The release of certain gases to the atmosphere is controlled in many countries owing to their negative impact on the environment and human health. These gases include carbon dioxide (CO2), sulfur oxides (SOx), nitrogen oxides (NOx), hydrogen sulfide (H2S) and ammonia (NH3). Considering the major contribution of greenhouse gases to global warming and climate change, mitigation of these gases is one of the world’s primary challenges. Nevertheless, the commercial processes used to capture these gases suffer from several drawbacks, including the use of volatile solvents, generation of hazardous byproducts, and high-energy demand. Research in green chemistry has resulted in the synthesis of potentially green solvents that are non-toxic, efficient, and environmentally friendly. Deep eutectic solvents (DESs) are novel solvents that upon wise choice of their constituents can be green and tunable with high biocompatibility, high degradability, and low cost. Consequently, the capture of toxic gases by DESs is promising and environmentally friendly and has attracted much attention during the last decade. Here, we review recent results on capture of these gases using different types of DESs. The effect of different parameters, such as chemical structure, molar ratio, temperature, and pressure, on capture efficiency is discussed.


Introduction
Climate change is an exceedingly critical environmental challenge, and its mitigation and remediation have gained widespread attention. Many countries around the world, have instituted laws and regulations to maintain environmental air quality and control the emission of pollutants that harm human health and affect the atmosphere [1]. Six major air contaminants have been identified based on National Ambient Air Quality Standards, including ozone, particulate matter, carbon monoxide, sulfur oxides (SOx), nitrogen oxides (NOx), and lead. Long-term exposure to these contaminants has been shown to have a harmful impact on human wellness over decades, evincing in a broad range of problems, including higher infant mortality rates and inherited respiratory diseases [2]. SOx and NOx, in particular, have serious effects on multiple human organs, damaging the nervous, respiratory, gastrointestinal, and cardiovascular systems to a degree that has been proven to be lethal. When gases such as SOx and NOx are transformed via chemical reactions, a portion of particulate matter is produced in the air. In the presence of sunlight, ozone is formed by chemical reactions between volatile organic compounds (VOCs) and NOx. Both SOx and NOx have harmful effects, in addition to their severe impacts on human health and climate, because they generate other air pollutants. A fossil-fuel driven plant releases approximately 80% of the NOx and 70% of the SOx present in the surrounding atmosphere, making oxide mitigation and elimination a critical task in automotive and industrial processes [3].
In the petrochemical industry, fuel is a primary source of pollutants in the environment, as it is rich in aromatics, nitrogen and sulfur-containing aromatic substances that are burned to create harmful contaminants. Thus, both the climate and human health can be influenced by the composition of fossil fuel oils [4]. Strict environmental standards to eliminate aromatics and sulfur-and nitrogen-containing fuel oil content have been implemented around the world to improve air quality. In short, harmful emissions are to be restricted by the generation of clean-burn fuel oils. In addition, the aromatic products of sulfur and nitrogen are troublesome in the refining of oil and gas because they are the sources of catalytic toxicity or deactivation, degradation and gum formation. High levels of aromatic content have been shown to affect the quality of the fuel; it is therefore important that aromatic compounds be separated from aliphatic ones [5]. Currently, hydrodesulfurization (HDS) is a proven desulfurization process that is widely used in the industry [6]. Aliphatic hydrocarbon sulfur content can be efficiently eliminated by HDS. However, because of their broad steric hindrance, it is difficult for polycyclic organic sulfides such as thiophene, benzothiophene, dibenzothiophene, and their derivatives to attain deep removal. Even if deep desulfurization can be accomplished, operating conditions are excessively harsh, resulting in a significant increase in the cost of desulfurization. Inhibition of the HDS process by the presence of nitrogen-containing compounds that poison the catalysts has also stimulated the need for denitrogenation. Hydrodenitrogenation is the most prominent denitrogenation process in the industry, but it involves harsh working conditions, and significant hydrogen consumption and capital costs. Furthermore, it is difficult to reach high denitrogenation efficiency [7]. The nitrogen content limit in diesel fuel has been regulated in many countries since 2011, and the allowed concentration was lowered from 70 ppm to <0.10 ppm. Comparably, in most countries, the sulfur content has been set to as low as 10 ppm (on an annual average basis) [8].
The rise in global temperatures constitutes an emergent risk to the earth, with an estimated 2 • C rise predicted by the end of this century [9]. The phenomenon of a gradual rise of average global temperature is known as the greenhouse effect and can be attributed to a group of greenhouse gases, of which carbon dioxide (CO 2 ) is the most dominant [10]. A direct cause of climate change is the steady annual growth of CO 2 , which is responsible for over 70% of the world's estimated greenhouse gases. Additionally, CO 2 has direct adverse health consequences on human health, with signs varying from acute breathlessness to lack of cognitive capacity, based on the degree and length of exposure to CO 2 . Such symptoms can be acute or chronic and can have a detrimental impact on human health if excessive CO 2 exists in indoor and outdoor air [11].
Various processes have been developed for the removal of toxic gases, including adsorption, absorption, and membrane separation [12,13]. Amine scrubbing is the most prominent among chemical absorption methods [14]. The most widely used amine solvents for CO 2 removal are monoethanolamine (MEA), diethanolamine (DEA), triethanolamine (TEA), diglycolamine (DGA), and methyldiethanolamine (MDEA). However, major downsides of amine scrubbing methods include the degradation of amines, the corrosion caused by the components produced during amine reactions with CO 2 and high regeneration energy ( Figure 1) [15][16][17]. Other good CO 2 absorbents include caustic solvents such as calcium hydroxide, potassium hydroxide, and sodium hydroxide [18]. Unfortunately, the regeneration of solvents remains a big concern. Carbonate solutions have also been employed for the absorption of acidic gases. While carbonate solutions have low volatility and result in a lower corrosion rate, they have major drawbacks in terms of lower absorption rates in comparison with caustic and amine solutions [19]. Compared to caustic and amine solutions, amino acid salt solutions have the benefit of improved regeneration owing to their lower volatility. However, the high molecular weight of amino acid salt solutions is a major drawback and increases the capital expenses of the absorber [20]. Owing to its simplicity of design, energy efficiency, and ease of scale-up, the use of membrane technology to capture CO 2 has seen rapid growth in popularity. Unfortunately, most membranes require regular replacement because they do not last long in practical industrial environments [21].  [15][16][17].
In recent decades, medicinal, chemical, and industrial processes have widely utilized solvents accounting for nearly 30% of emissions of VOCs and 60% of industrial emissions worldwide [22]. Green processes in all areas of chemistry and engineering have drawn significant attention over the past 20 years, representing an increasing desire to minimize the usage of hazardous and unsafe chemicals and to raise understanding of environmental concerns. Green chemistry and engineering is also responsible for limiting or eliminating the usage of harmful and hazardous chemicals and for designing ecologically sustainable chemical procedures [23]. Solvents comprise a significant field of research in green chemistry with most of the traditional chemicals being toxic and flammable. Therefore, researchers have established many safer alternatives, such as water-based or solvent-free systems, ionic liquids (ILs), and supercritical fluids (SCF), with the solvent-free system representing the best-case scenario [24,25]. However, the use of solvents cannot always be eliminated because of their pivotal role in heat and mass transfer, and dissolution and separation operations [26]. For example, water, the world's most abundant compound, has already been used in a number of chemical processes as a solvent. Even so, the drawbacks of using water as a solvent include the negligible solubility of various organic compounds and the possibility of contamination, with a further downside posed by the high vaporization energy of this solvent. Another solution is to substitute typically organic solvents with SCFs; that are chemically stable, easy to handle, and safe. However, owing to their non-polar existence, SCFs still have some drawbacks, e.g., CO 2 has minimal dissolving capacity for polar solutes [27].
Since the early 2000s, ILs, a form of newly synthesized solvents, have garnered a great deal of attention from the research community in multidisciplinary fields. ILs are molten salts, composed of ions, with a melting point below 100 • C [28,29]. The main aspects of ILs over conventional organic solvents are their minimal vapor pressure, good thermal characteristics, wide liquid range, miscibility, solubility range, and chemical reaction suitability. Nevertheless, studies indicated that the 'green' characteristics of ILs are at least questionable because of the known drawbacks of these solvents; for example, high preparation costs, high viscosity, equivalent or higher toxicity, and poor biodegradability compared to organic solvents [30,31].
Deep eutectic solvents (DESs) have become attractive replacements for traditional solvents and ILs in order to tackle the high levels of toxicity and costs of ILs. However, the definition of DESs remains controversial, and different definitions do not discriminate DESs from other mixtures, as all mixtures of immiscible solids are eutectic and various compounds may form hydrogen bonds when mixed [32]. The concept of DESs as a new class of sustainable solvent was first coined by Abbott et al., and identified as solvents with melting points significantly lower than those of individual components when combined in a proper molar ratio [33]. DESs consist of large, nonsymmetric ions with low lattice energy and thus low melting points and are usually produced by the mixing of a metal salt or hydrogen bond donor (HBD) and a quaternary ammonium salt. The delocalization of charges between HBD and, for example, a halide ion via hydrogen bonding allows the melting points of the mixture to decrease in comparison with the melting points of the individual constituents. Recently, Martins et al. [34] defined DES as a blend of two or more components with a eutectic temperature that is lower than that of an ideal liquid mixture, with substantial negative deviations from ideality (∆T 2 > 0). ∆T 2 indicates the depression in temperature, which is the difference between the ideal and real eutectic point. Furthermore, these authors indicated that it is critical that, irrespective of the composition of the mixture, the temperature depression contributes to the liquid mixture at the operating temperature.
Although DESs and traditional ILs have different chemical properties, they have similar physical properties, especially their capacity to be tailored to a specific form of chemistry as tunable solvents. They also possess low vapor pressure, a relatively broad liquid-range, and non-flammability [35]. DESs have many benefits over conventional ILs, such as easy preparation and a convenient supply of comparatively cheap materials (the components themselves are toxicologically well characterized, so they can be conveniently transported for manufacturing on a broad scale); they are, however, less chemically inert in general. The preparation of DESs requires the simple mixing of two or more compounds, usually with moderate heating. With respect to traditional ILs (e.g., imidazolium-based liquids), this yields a relatively low preparation cost and enables large-scale applications. The toxicity of ammonium-based DESs toward bacterial and eukaryotic cells was first investigated by Hayyan et al. [36] and no inhibition of bacterial growth was observed. However, DESs based on phosphonium salts were found to be cytotoxic under the same conditions [37]. Mao et al. [38] found that the toxicity of ChCl-based DESs toward Arthrobacter simplex was lower than that of the individual components. The toxicity and biodegradability of DESs toward various organisms (such as, bacterium, Escherichia coli) was assessed by Wen et al. [39]. The investigated DESs were toxic to bacteria at concentrations above 75 µM and inhibited bacterial growth by the DESs was much more than that of their individual components. Radosevic et al. [40] investigated the toxicity of three ammonium-based DESs, utilizing fish and human cell lines to measure the in vitro toxicity. All examined DESs were rated as readily biodegradable based on their high degree of mineralization. Many researchers have indicated that DESs has minimal or negligible volatility relative to traditional organic solvents. However, recently, Chen et al. [41] reported the volatilization of ChCl:N-methylacetamide (1:6) DES even at room temperature and pressure. Another study conducted by the same group [42] found that the polyethylene glycol (PEG)-based DESs showed volatilization under the same conditions. It is obvious that a better understanding of DESs volatility and toxicity needs more research before these solvents can really be claimed to be less-volatile, biodegradable and non-toxic. A few merits and disadvantages of DESs are presented in Figure 2.
DESs play a significant role in the solubility of gases and liquid-liquid extraction (LLE). Our group [43] compared the performance of classical amine solvents (widely used in the industry for this purpose) and the amine-based DESs for CO 2 capture. The results showed that only 10% of the amine reacted with the CO 2 while for the aqueous solution of MEA, all of the amine reacted with the CO 2 . Hence, if only 10% of the amine in the DES reacts with CO 2 , this means that the energy needed for desorption is much less than that in amine aqueous solution. In another application related to the use of DESs for separating aromatics from aliphatics, it was noticed that when sulfolane-based DES was used as liquid-liquid extractant, no DES was found in the raffinate layer [44]. While when pure sulfolane was used, its concentration in that layer reached 20 wt%; causing solvent loss and requiring additional purification steps. The same behavior could be predicted for desulfurization and denitrification exposed in this review.
In 2015, García et al. [45] presented a review on the applications of DESs for gas solubility, with special attention to CO 2 capture. Some other reviews involving the capture of CO 2 via DESs have also been published [46][47][48]. In this work, we present a critical review for the use of different types of DESs in capturing CO 2 . Because some reviews about this topic have already been published, we limit the review to the articles published starting from 2015; however, we give more attention to articles published recently. Chen et al. [49] provided a review on the capture of toxic gases by DESs. However, the review about the desulfurization and denitrification of fuels using DESs was not presented. In this study, the use of DESs in the absorption of other hazardous gases, e.g., SOx, NOx, NH 3 , etc. will be discussed in detail. Furthermore, we will also present in dept review about the desulfurization/denitrification of fuels via DESs. Finally, challenges, opportunities, and perspective of the commercial use of DESs will be discussed. The main topics of this study are as follows: Capture of acidic gases • Selectivity of DESs in capturing gases • Desulfurization and denitrification of fuels

CO 2 Capture
Chemical absorption, especially amine-based processes, is one of the preferred options for capturing CO 2 . However, this process involves some major drawbacks, including the high cost of this technology associated with extensive energy penalties, solvent degradation, and high corrosion [51,52]. The cost of CO 2 separation using amine-based technology is in the range of US $50 to US $100 per ton of carbon, which is very high for most of the applications [53]. DESs have become desirable solvents for various gas technology applications due to their beneficial characteristics, such as biodegradability, good thermal and chemical stability, non-flammability, high solvation capability, low-cost, and ease of preparation. This article provides a comprehensive review of the potential applications of DESs for CO 2 capture based on recent studies. Various studies concerning the capture of CO 2 via DESs have already been published; therefore, in this article, we have considered studies published since 2015. Choline chloride (ChCl)/urea (1:2) is one of the most widely investigated DES for CO 2 capture. The solubility of CO 2 was first measured in ChCl/urea (1:2) DES at 313.15, 323.15, and 333.15 K and at pressures up to 13 MPa [54]. Many factors influence the solubility of CO 2 in DESs, including pressure, temperature, the type of hydrogen bond acceptor (HBA) or HBD, the HBA:HBD molar ratio, viscosity, and the water content of DESs. Table 1 displays the solubility data of CO 2 in various DESs at different temperatures and pressures. We have only included DES systems with CO 2 solubility higher than 0.1 mol CO 2 kg −1 solvent. The unit for the comparison of CO 2 capture is mol·kg −1 , except as otherwise mentioned. Deng et al. [58] examined the effect of the HBA of DESs on CO 2 solubility in five LV-based DESs as illustrated in Figure 3a. All DESs were prepared at 1:3 HBA to HBD molar ratio. At fixed temperature (i.e., 303.15 K) and pressure (~0.55 MPa), ACC/LV and TBAC/LV DESs demonstrated the highest CO 2 absorption capacity (around 0.3), while TEAB/LV had the lowest value (0.24). Sarmad et al. [61] also investigated CO 2 capture by various DESs with the HBD as acetic acid (AC). The effect of HBA in the DESs for CO 2 capture was ordered as follows: BTMA (1. MPa. These variations were due to the interactions between CO 2 and functional groups in the HBD. The intermolecular hydrogen bonds are stronger in LA than in AC or LV because of the proximity of the hydroxyl group to the carboxylic group. Hence, it is not easy to break intermolecular hydrogen bonds for contact with CO 2 . Furthermore, acetic acid has the weakest intermolecular hydrogen interactions; therefore, acetic acid molecules can readily interact with CO 2 , yielding higher CO 2 solubility compared to other DESs. For acetic acid-based DESs, the solubility of CO 2 increases with increasing alkyl chain length of the HBA. For instance, when the alkyl chain length increased from ethyl to butyl (i.e., from tetraethylammonium to tetrabutylammonium), the solubility of CO 2 increased from 1.177 to 1.411 mol·kg −1 . Similar behavior was reported by Zubeir et al. [62]; i.e., the solubility of CO 2 increased by increasing the alkyl chain length from methyltrioctyl-to tetraoctylammonium. Moreover, an increase in carbon atoms in the HBD alkyl chain increases CO 2 solubility. This can be attributed to the increase in free volume with increasing alkyl chain length, resulting in higher CO 2 solubility [64]. Li et al. [65] synthesized a series of DESs by mixing different ammonium salts such as HBA and MEA, DEA, MDEA, and TEA as HBDs for CO 2 absorption. The solubility of CO 2 followed the following trend: ChCl ≈ TMAC > TEAC > TEAB > TBAC > TBAB, while for HBD, the order is MEA > DEA > MDEA > TEA. MDEA and TEA showed low CO 2 absorption because of the absence of hydrogen on the nitrogen atoms. The solubility of CO 2 using ChCl and TMAC was almost the same because both salts have similar chemical structures. In Figure 3d, the effect of HBD of ACC-based DESs was investigated at 303.15 K. ACC-based DESs were prepared by mixing with LV, guaiacol (GC), and imidazole (imi) at a 1:3 molar ratio. The order for CO 2 solubility was ACC/LV (0.3) > ACC/imi (0.29) > ACC/GC (0.18).
The nature/type of salt of DESs also plays a crucial role in CO 2 capture. Deng et al. [58] used five ammonium salts (ACC, TEAB, TEAC, TBAB, and TBAC) to prepare DESs for CO 2 capture. For ammonium salts, DESs with larger cations showed higher CO 2 solubility, and the cations of the salts dominated the absorption capacity for CO 2 capture. The performance of various ammonium-and phosphonium-based DESs for CO 2 capture is compared in Figure 4 [43,61]. Both types of DESs with MEA as the HBD resulted in higher CO 2 solubility than the DEA-and TEA-based DESs. The solubility of CO 2 increased by increasing the HBA:HBD molar ratio for ChCl/EA DESs; however, the opposite was true for MTPPB:MEA DES [66].
In general, the solubility of CO 2 in DESs increases with decreasing temperature and increasing pressure. Sarmad et al. [61] investigated the effect of pressure on the CO 2 capture via various DESs, as shown in Figure 5. As expected, the solubility of CO 2 in the DESs increased with increasing pressure and decreasing temperature for the systems examined. The decrease in solubility with increasing temperature can be understood using the concept of the kinetic energy of the gas molecules: as it increases with increasing temperature, causing breakage of intermolecular bonds between the gas molecules that are formed within the solute, and these have a higher tendency to escape from the solution.  Usually, the solubility of CO 2 in the DESs follows Henry's Law (Equation (1)), i.e., the solubility of CO 2 is proportional to its partial pressure. Deng et al. [58] also investigated the effect of pressure on CO 2 solubility in five LV-based DESs. They found that the solubility of CO 2 in DESs is proportional to the gas phase's equilibrium pressure, indicating that the CO 2 absorption via DES is a physical phenomenon. Figure 5a depicts the CO 2 solubility as a function of pressure in various DESs. It is evident from the figure that the solubility increases with increasing pressure for all the DESs. Figure 5b shows the effect of pressure on TEAC/LV (1:3) at different temperatures. Solubility trends have shown that the CO 2 absorption capacity increases with decreasing temperature and increasing pressure.
The degree of gas solubility in a solvent is often assessed using Henry's law constant (k H ) [67]: where x i is the mole fraction of gas in the solution, and f i is the gas fugacity in vapor phase. Liu et al. [57] reported that the solubility of CO 2 increases with an increase in the mole fraction of ChCl/GC, DEH/GC, and ACC/GC from 1:3 to 1:5 at a fixed pressure and temperature, indicating that GC plays a major role in the solubility of CO 2 in DESs. For example, the solubility of CO 2 using ChCl/GC increased from 0.171 to 0.188 when molar ratio was changed from 1:3 to 1:5. Furthermore, the effect of the molar ratio of DESs on Henry's law constant of CO 2 absorption was also obvious. Among GC-based DESs, DEH/GC (1:5) showed the lowest Henry's law constant, i.e., higher CO 2 solubility at a fixed temperature and pressure. The effect of the molar ratio of different amine-based DESs on the solubility of CO 2 was also investigated [66]. The solubility of CO 2 increased with a decrease in the molar ratio of ChCl/MEA and ChCl/DEA DESs from 1:6 to 1:10, indicating that addition of MEA or DEA can increase both the chemical and physical absorption of CO 2 . However, Ghaedi et al. [60] found that by increasing the molar ratio of phosphoniumbased DESs including ATPPB/diethylene glycol (DEG), and ATPPB/triethylene glycol (TEG) from 1:4 to 1:16, the solubility of CO 2 decreased as shown in Figure 6. This result demonstrated that ATPPB plays an important role in CO 2 capture. At the same time, glycols play a minor role. Ren and co-workers [68] explored the effect of L-arginine/gly molar ratios (1:5, 1:6, and 1:7) on the solubility of CO 2 .
Many DESs are highly hygroscopic and tend to absorb water easily [69]. Ren et al. [68] exploited the hydrophilic nature of DESs for CO 2 capture. DESs with varying water content have been tested for CO 2 capture to explore the effect of water content on CO 2 solubility. They found that the efficiency of CO 2 capture could be increased by adding a small amount of water to the DES. Ma et al. [70] investigated the effect of water on CO 2 solubility using glycerol-based DESs. Most of the glycerol-based DESs have high viscosity; however, for some DESs, viscosity changes drastically when a small amount of water is added [71]. For instance, the viscosity of BTMA/gly (1:2) DES was reduced from 716 to 20 mPa·s after adding a small quantity of water (0.11 mole fraction). Furthermore, CO 2 absorption increased by 25% using BTMA/gly (1:2) with 0.11 mole fraction of water. However, the solubility of CO 2 was reduced by further increasing the water content owing to the low solubility of CO 2 in water. Trivedi et al. [72] examined the absorption of CO 2 in the presence of varying water content (5-20 wt%) with monoethanolamine hydrochloride /ethylenediamine (1:3) DES. With an increase in water content, the initial uptake kinetics were improved, i.e., when the water quantity increased from 0 to 20 wt%, CO 2 uptake increased from 25.2 to 28.1 wt%.

Capture of Acidic Gases
Nitric oxide (NO), nitrogen oxide (NO 2 ), ammonia (NH 3 ), sulfur dioxide (SO 2 ), and hydrogen sulfide (H 2 S) are considered toxic industrial gases [49]. The burning of coal mainly produces NO 2 and NO. Large amounts of these oxides (NO and NO 2 ) can cause acid rain, acid mist, destruction of ozone, and harm to human health. NH 3 is often generated from waste gas during the synthesis of ammonia, which causes air pollution and rhinitis/pharyngitis and facilitates the formation of particulate matter. During the combustion of fossil fuels from industrial waste gas or volcanic eruptions, toxic SO 2 is produced. Air pollution, human cancer, and acid rain result from the release of large quantities of SO 2 [73]. H 2 S is another acidic gas produced from natural gas treatment, decomposition of bacteria, and industrial refineries. H 2 S has high toxicity and corrosiveness. Due to the high risk of these acidic gases (i.e., SO 2 , NH 3 , H 2 S, NO 2, and NO), highperformance, low-cost, and highly sustainable processes are required to capture them. It is clear that toxic gas capture can enhance air quality, reduce air pollution, and preserve the ozone layer. In addition, the captured gas can be utilized in other processes. Hence, it is imperative to have green routes to capture these toxic gases with better efficiency and selectivity.

Oxide-Based Acid Gases
Yang et al. [80] investigated the solubility of SO 2 in ChCl/gly DES with different molar ratios. Figure 7 shows the effect of ChCl/gly DES molar ratio on the solubility of SO 2 at different temperatures. The highest SO 2 solubility (0.678 g SO 2 /g DES) using ChCl/gly was achieved at 1:1 molar ratio, 0.1 MPa, and 293. 15 K. An increase in the HBD molar ratio from 1:1 to 1:4 at fixed pressure and temperature reduced the SO 2 absorption capacity. For instance, at 293.2 K and 0.1 MPa, the solubility of SO 2 was reduced from 0.678 to 0.320 (g SO 2 /g DES). The effect of a mole fraction of ChCl/gly DES on Henry's law constant of SO 2 absorption was also evident. Henry's law constant increased with decreasing concentrations of ChCl in the DES. The same group [104] investigated the solubility of SO 2 in another DES formed by combining EMIMC with EG under different operating conditions. The absorption capacity of SO 2 increased (0.82, 1.03 to 1.15 g SO 2 /g DES) with an increase in the ratio of EMIMC in EMIMC:EG DES (from 1:2 to 1:1 and 2:1). The same group prepared EMIMC-based DESs by mixing EMIMC with either TEG or succinonitrile (SNT) to investigate the SO 2 absorption capacity [105]. The SO 2 absorption capacity increased with an increase in the molar ratio of EMIMC in the EMIMC/TEG DES. The highest capacity of 1.25 g SO 2 /g DES was achieved in the EMIMC/TEG at a 6:1 molar ratio.
It is interesting to note that in some cases, increasing the molar ratio of HBD increased the SO 2 solubility. In contrast, in other cases, the solubility was increased by increasing the molar ratio of HBA. For example, the solubility of SO 2 increased when the molar ratio of ChCl or EMIMC in ChCl/phenol, ChCl/gly, EMIMC/EG, EMIMC/TEG and EMIMC/FMP DESs was increased [82,89]. However, SO 2 solubility increased with increasing molar ratio of imidazole in ACC/imidazole DES because imidazole exhibited a strong interaction with SO 2 [74]. A significant change in SO 2 solubility was observed with the change in the molar ratio of ChCl and EMIMC-based DESs; however, that is not true for all DESs. For instance, betaine:EG and caprolactam:EG showed almost no change in SO 2 absorption at different molar ratios (1:3 to 1:5) [49,76]. Similarly, a change in the molar ratio of PPZB/gly DES had almost no effect on the capacity of SO 2 [94].

NOx Capture
A limited number of studies have reported on the absorption of NO via DESs. Zhang et al. [92] used imidazole/gly (1:2) to capture NO. They used the same DES to capture SO 2 and found that it had a very low capacity (0.034 mol NO/mol DES) for NO compared to SO 2 (0.643 mol SO 2 /mol DES). Azole-based DESs were found to be efficient at dissolving NO. Zhang et al. [84] used four azole-based low-viscosity DESs to capture NO. TBPC/Tetz (1:1) exhibited the highest NO absorption capacity: 2.10 mol NO/mol DES at 0.1 MPa and 303.2 K. These researchers also studied the effect of temperature on the absorption capacity of NO, as shown in Figure 9a. The absorption capacity of NO decreased linearly with the increase in temperature. The authors found that there were chemical interactions between the hydrogen attached to the ring containing the nitrogen atom of Tetz and NO. The effect of HBA in DESs on the solubility of NO was also examined. The effect of HBA in DESs on NO capture at 0.1 MPa and 303.2 K was as follows: TBPC/Tetz > TBAC/Tetz > TBPB/Tetz > TBAB/Tetz. Moreover, lower NO pressure and higher temperature reduced the absorption capacity of the DESs. Sun et al. [107] explored the application of amine-based functional DESs for the capture of NO. The DESs were prepared by mixing ammonium salts with polyhydric alcohols, and all DESs showed good absorption capacity for NO (10 vol%). Sun et al. [107] also investigated the effect of temperature on the DES absorption capacity of NO. For example, the absorption capacity decreased from 0.33 to 0.18 mol NO/mol DES, with increasing temperature from 303.2 to 323.2 K in tetraethylenepentamine chloride (TEPA)/EG (1:3) DES. This could be attributed to the weak binding forces between NO and DES at higher temperatures. Owing to the increase in temperature, the equilibrium shifted in the opposite direction, causing reduction in the NO absorption capacity.
The effect of the molar ratio of DESs on the absorption capacity of NO was also investigated. For instance, NO absorption capacity increased from 3.10 to 4.52 mol NO/mol DES when the molar ratio of TEPA/EG changed from 1:1 to 1:3.
No change in the molar absorption capacity of NO was observed when the molar ratio further changed from 1:4 to 1:6. However, the mass absorption capacity of NO was reduced with the increase in EG from 1:4 to 1:6, which indicated that the active constituent affecting the NO absorption capacity was TEPA [107]. In another study, Sun et al. [96] reported that the absorption capacity of NO increased for TBPB/DMTU DES as the molar ratio increased from 1:1 to 1:3. The effect of water on the absorption capacity of NO was also explored, and no significant change in the NO absorption capacity by TEPA/EG (1:3) DES was observed under different levels of water content [107]. For example, the mass absorption capacities of NO using TEPA/EG (1:3) DES were 0.30 and 0.32 mol NO/mol DES when the water content of the DES was 18.3 and 0.1 wt%, respectively. However, the mass transfer rate was improved with increasing water owing to a reduction in the viscosity of the DES.
Although applications of DESs for the capture of acid gases continue to emerge, DES absorption of NO 2 is still in the embryonic stage. Recently, Chen et al. [81] studied the absorption of NO 2 by ChCl-based DESs and their aqueous mixtures. The effect of the partial pressure of NO 2 on the absorption capacity of DESs was analyzed at 298.15 K, as shown in Figure 9b. With decreasing NO 2 partial pressure, the solubility of NO 2 was reduced. For example, the solubility in ChCl/gly (1:2) was reduced from 0.356 to 0.027 gNO 2 /gDESs when the partial pressure was decreased from 101.3 to 0.01 MPa. The effect of the molar ratio of DESs on the absorption capacity was also investigated, and the solubility was increased with increasing molar ratio. The effect of water content on NO 2 absorption capacity was also explored. With the addition of 3-6 wt% water, the solubility of NO 2 in the DESs showed the following trend: ChCl/gly (1:2) > ChCl/EG (1:2) > ChCl/gly (1:4) > ChCl/EG (1:4). With high water content (more than 50 wt% water), NO 2 absorption is unfavorable. At this water concentration, the DES becomes unstable, and a complex hydrogen bond network among the components of the DES and water is formed, as reported previously [81].
Other studies relevant to the absorption of NO 2 in DESs were based on theoretical calculations alone. For instance, the absorption mechanism of NO 2 in ChCl DESs with urea, methyl urea, and thiourea as HBD was investigated using quantum chemical methods [108]. Based on quantum calculations, ChCl/thiourea was found to be more favorable for denitrification. However, experimental data are needed to verify such predictions.

NH 3 Capture
The excellent benefits of simple synthesis and high tunability have yielded a wide range of prospects for evolving DESs. Various configurations and combinations of HBA and HBD make DESs rich and diverse, affecting the physicochemical properties of these DESs and their ability to absorb NH 3 . This section focuses on the solubility of NH 3 by various DESs. As illustrated in Table 3, NH 4 SCN, ChCl, and 1-ethyl-3-methylimidazolium ([emim]Cl) are the most widely used HBAs to absorb NH 3 . These HBAs are usually mixed with HBDs such as glycerol, EG, urea, benzoic acid, LV, and phenol to form DESs in a specific molar ratio.  The effect of the HBA and HBD of DESs is depicted by heat map induction, as shown in Figure 10. For the same molar ratio (1:2), ChCl-based DESs showed the following order for NH 3 solubility: LV > gly > PNA > EG > TFA > urea > MU. During absorption by DESs, white solid particles were formed with the acidic HBDs (LV or PNA), which severely hindered NH 3 interaction with the remaining absorbent and prevented further absorption. The breaking up of the supramolecular structure in the DES resulted in solid formation. This mechanism's adverse consequence is well illustrated by the peculiar relationship between acidity and capacity in these solvents' absorption.
Since carboxylic acids are even more acidic than alcohols and urea, DESs containing carboxylic acids as HBDs were assumed to have a higher NH 3 uptake ability than ChCl/gly, ChCl/EG, and ChCl/urea. However, these predicted outcomes were not achieved [115]. This unexpected acidity-capacity relationship revealed that the well-recognized approach to increase the solubility of simple solutes by raising the acidity or their number of acidic groups of solvents is not generally true in the case of DESs because of the fragile supramolecular structure. In order to prevent this structural breakage, ternary DESs can be prepared by adding neutral donors. However, the opposite behavior was observed when acidic HBAs were used. For instance, Deng et al. [109] compared the performance of three azole-based DESs, and found that NH 3 solubility increased with increasing HBA acidity as follows: tetrazole/gly > 1,2,4-triazole/gly > imidazole/gly. They also investigated the effect of HBD of DES on the solubility of NH 3 . Triazole was mixed with six different HBDs (caprolactam, acetamide, glycerol formal, DL-1,2-isopropylidene glycerol, EG, and glycerol). Higher solubility of NH 3 was observed for the DESs containing a hydroxyl group as the HBD.
The addition of a third component to the binary DESs can affect the solubility of NH 3 . Zhong et al. [123] prepared a ternary DES by combining ChCl with EG and tetrazole and compared the solubility of NH 3 of ternary DES with ChCl/EG and EG. ChCl/tetrazole/EG (3:7:14) showed greater absorption capacity compared to ChCl/EG (3:14) and EG. Moreover, ChCl/EG (3:14) exhibited the lowest NH 3 solubility, demonstrating that the less-active component of NH 3 solubility is ChCl. ChCl/tetrazole/EG (3:7:14) demonstrated higher NH 3 capacities than EG at different pressures, indicating that tetrazole has the largest effect on NH 3 capture. Furthermore, the capacities of NH 3 in DESs were more pronounced at low pressures. For instance, using ChCl/tetrazole/EG (3:7:14), the solubility of NH 3 was five times that in EG at 0.01 MPa and 313.2 K, while its solubility in ChCl/tetrazole/EG (3:7:14) was only 1.2 times that in EG at 0.1 MPa and 313.2 K. Figure 10. NH 3 solubilities in DESs based on different HBAs and HBDs at 313.2 K and around 0.1 MPa. EACl/gly, 1,2,4-triazole/gly, imidazole/gly, tetrazole/gly were mixed in 1:3 HBA:HBD molar ratio. NH 4 SCN/gly and NH 4 SCN/urea were obtained by mixing in 2:3 molar ratio. All other DESs were prepared in 1:2 molar ratio [109,111,115,116,121]. Figure 11 illustrates the effects of pressure, temperature, and DES molar ratio on the absorption capacity of NH 3 [117]. NH 3 absorption capacity increased with increasing pressure and decreasing temperature, which is a common behavior for gas absorption via liquids. However, for EACl-based DESs, as the temperature increased, the variation in NH 3 solubility steadily faded, meaning that the strength of the hydrogen bond interactions between NH 3 and EACl was negatively dependent on temperature. However, the isothermal profiles varied considerably from the ideal form, possibly because of the close interaction between EACl and NH 3 . EACl was thus the primary component in NH 3 absorption mixtures. This assessment can also be concluded by comparing NH 3 solubilities in EACl/acetamide DES mixtures with different EACl/acetamide molar ratios. EACl/acetamide 1:1 mixture had higher NH 3 solubility owing to its higher EACl content compared to 1:2 and 1:3 molar ratios. A similar behavior was observed with EACl/ureabased DESs, i.e., the absorption capacities of NH 3 decreased with increasing urea content in the EACl/urea mixtures [119]. However, for EACl/gly DESs, NH 3 solubility decreased with increasing mole fraction of EACl in the DES. The order of capacity for EACl:gly DESs molar ratios was as follows: 1:5 > 1:4 > 1:3 > 1:2. For ternary DESs, there was no clear trend for NH 3 solubility. For instance, the solubility increased (from 0.071 to 0.096 gNH 3 /gDES) when the ChCl/PNA/gly DES molar ratio increased from 1:3:1 to 1:3:3. However, the solubility was reduced (from 0.096 to 0.095 gNH 3 /gDES) after the molar ratio was further increased from 1:3:3 to 1:3:5. Similarly, ChCl/resorcinol (RES)/gly absorption capacity increased from 1:1:5 to 1:7:5 and then dropped sharply when the molar ratio was further changed to 1:9:5 [115]. This indicates that optimal mole fractions of DESs (either binary or ternary) are needed to enhance gas absorption. Furthermore, higher NH 3 solubilities were observed at lower temperatures for EACl/acetamide, EACl/urea, and EACl/gly DESs. Figure 11. Effect of pressure, temperature, and molar ratio on the absorption capacity of NH 3 through EACl/acetamide based DESs; solid, dash, and dot lines indicate the 1:1, 1:2, and 1:3 EACl/acetamide molar ratios, respectively. Data are taken from [117].
The low viscosity characteristic of any solvent is favorable for the liquid transport and mass transfer of gas. The NH 3 absorption was swift (with the equilibrium time being shorter than 1.5 min) in the azole-based DESs owing to their lower viscosity (<30 mPa. s at 298.2 K) [123]. GI/acetamide (1:2) DES also exhibited fast NH 3 absorption owing to its low viscosity (21.05 mPa. s at 298.2 K), and the NH 3 pressure was drastically reduced to a constant within around 100 s [120]. NH 3 absorption capacity to achieve equilibrium was less than 60 s in EACl/phenol DESs, mainly due to their relatively low viscosities [118]. EACl/phenol DESs were prepared in different molar ratios. However, there was no significant difference between the NH 3 solubility because there were minimal viscosity changes. Similarly, ternary DESs ChCl:tetrazole:EG (3:7:14) also resulted in very fast NH 3 absorption (equilibrium time was less than 1.5 min) due to the low viscosity of DES (27.4 mPa. s at 298.2 K) [123].

H 2 S Capture
Liu et al. [124] found that H 2 S absorption capacity increased with increasing molar ratio of ChCl/urea DES from 1:1.5 to 1:2.5 at a fixed temperature and pressure. Furthermore, the absorption capacity of H 2 S in ChCl/urea DESs was decreased linearly by increasing the temperature. Carboxylic acid-based DESs showed higher solubility compared to ChCl/urea DESs [125]. For instance, the absorption capacity of H 2 S in ChCl/urea (1:2) is 0.38 (mole H 2 S/kg DES) at 313.2 K and 0.2 MPa, while it is 0.70 (mole H 2 S/kg DES) in ChCl/propionic acid (PA) (1:2) at 298 K and 0.184 MPa. The solubility of H 2 S in carboxyl acid-based-DESs was ordered as follows: TBAB/PA (1:1) > TBAB/AC (1:1) > TBAB/formic acid (FA) (1:1) > ChCl/PA (1:2) > ChCl/AC (1:2) > ChCl/FA (1:2) at 298 K and around 0.5 MPa. The effect of HBA on the solubility of H 2 S was also evident; i.e., for the same HBD, TBAB-based DESs showed higher H 2 S solubility compared to ChCl-based DESs. The hydrogen bond strength of TBAB-based DESs is lower than that of the ChCl-based DESs, and ChCl consists of a hydroxyl group; therefore, the resulting hydrogen bonding interactions in ChCl-based DESs are more complex than those in TBAB-based DESs. Recently, supported DESs using fumed silica (supporting material) and DES as the loading substance were developed to capture H 2 S [126]. Triethylamine hydrochloride (TEAC) and cupric chloride (CuCl 2 ) were mixed at a 1:1 molar ratio to prepare the DES. The highest H 2 S capacity of 9.97 mg/g DES was obtained at a 10% DES loading rate and 303.2 K. Furthermore, it was also found that TEAC/CuCl 2 (1:1) was more efficient as a loading substance than pure TEAC or CuCl 2 .

Selectivity of DESs in Capturing Gases
SO 2 and CO 2 are two typical gases that coexist in the flue gas. Thus, it is more important to selectively capture SO 2 from simulated mixed gases containing both SO 2 and CO 2 . Deng et al. [75] determined the SO 2 /CO 2 selectivity (S) in six LV based DESs and compared the results with some ILs. Higher SO 2 /CO 2 selectivities  were obtained using all six DESs than in the ILs (3-4 times higher). Therefore, LV-based DESs could be used as efficient absorbents for the selective capture of SO 2 from CO 2 in flue gas. Liu et al. [82] compared the performance of six phenol-based DESs for the selective absorption of SO 2 . Selectivity of SO 2 /CO 2 using the phenol-based DES were as follows:  [75]. However, cardanol-based DESs had lower selectivity than GC-based DESs because the alkyl long chains in cardanol showed that weak interactions with SO 2 and GC have clearly better capability to interact with SO 2 . Evidently, the increased molar ratio of phenols (GC or CD) to ChCl in DESs resulted in the decreased SO 2 /CO 2 selectivity. The similar trend was observed for PPZB/gly DESs [94]. The order of selectivity in terms of PPZB/gly molar ratio was as follows: 1:4 (S = 33.1) > 1:5 (S = 12.8) > 1:6 (S = 9.5).
In industrial streams, other gases coexist with NH 3 , such as CO 2 and N 2 . Therefore, it is imperative for solvents to capture NH 3 as well as to exhibit higher selectivity for NH 3 than for other gases. Li and co-authors [115] compared NH 3 /CO 2 selectivity for binary and ternary DESs. ChCl/RES/gly (1:3:5) exhibited higher NH 3 /CO 2 selectivity (142) than binary DES ChCl/RES (1:3) (64), indicating that the addition of glycerol to the binary DES did not increase the CO 2 solubility but contributed to a much higher NH 3 solubility. Furthermore, when resorcinol was replaced with phenol in ternary DES, lower selectivity (87) was recorded than in resorcinol-based ternary DES. When phenol was mixed with EACl in a 1:7 salt: alcohol molar ratio, better NH 3 /CO 2 selectivities (S = 151-195 at 298.2-353.2 K) were demonstrated [118]. From the above discussion, it is obvious that glycerol as HBD and EACl as HBA play a significant role in the selective removal of NH 3 from CO 2 . Therefore, EACl was mixed with glycerol at 1:2 molar ratio, and these exhibited excellent NH 3 /CO 2 selectivities ranging from 818 to 5567 [116].

Desulfurization and Denitrification of Fuels
Because of limited available resources, oil refiners are presently processing crude oil with a higher content of sulfur and nitrogen compounds. The removal of sulfur and nitrogen is one of the major challenges in the fuel processing industry. Sulfur is usually found in fuels in the form of compounds such as thiophenes, mercaptans, and derivatives, which contribute to the emission of sulfur oxides during combustion. A number of studies on extraction desulphurization and denitrification using DESs have been reported to date. The extraction efficiency is dependent on the type of DESs used; therefore, the selection of suitable DESs is significant. Some important factors influencing the performance of DESs for sulfur and nitrogen removal include: molar ratio, type of HBA or HBD, and extraction temperature.
The sulfur removal efficiency is significantly dependent on the type of HBA and HBD. Li et al. [6] compared the performance of different HBA and HBDs in the DESs for the removal of sulfur. For the same HBD and molar ratio, the sequence for HBAs for sulfur removal efficiency was as follows: TBAC > TMAC > ChCl. The alkyl ammonium chloride-based DESs exhibited higher removal efficiency for benzothiophene than ChClbased DES. The extraction sequence for HBDs was as follows: polyethylene glycol > propionate > EG > TEG > glycerol > malonic acid. Among HBDs, polyol-based DESs depicted higher extraction efficiency [extraction efficiency up to 71.06% using TBAC/PEG (1:2)]. Using acids as HBDS, the desulfurization efficiencies of some DES HBDs were as follows: p-toluenesulfonic acid (PTSA) > 5-sulfosalicylic acid > 4-aminosalicylic acid. A positive correlation was observed between DESs acidity and desulfurization efficiencies; i.e., DES with stronger acidity exhibits higher desulfurization capabilities [134]. Li and coauthors [135] also investigated the effect of different acidic HBDs of DES on the extraction of sulfur compounds. DESs were prepared by mixing acidic HBD with TBAB. The extraction capacity of different sulfur compounds was as follows: FA~AC~PA > oxalic acid (OA) > MA > adipic acid (AD) for thiophene; FA > PA > AC > OA > MA > AD for benzothiophene; PA > AC > OA > FA > MA > AD for dibenzothiophene. Regarding the nitrogen compound, a maximum removal efficiency of around 98.2% of carbazole was reported using ChCl/PNA (1:2) DES, while ChCl/MA (1:1) showed a very low efficiency of around 34.6% [7].
Concerning extraction temperature, studies [136][137][138] reported that the extraction efficiencies of sulfur content are reduced with increasing extraction temperature. A high temperature range was found to be unfavorable for the extraction of sulfur compounds using DESs. Warrag et al. [139] reported that the extraction temperature had a slight effect on the extraction efficiency of thiophene, attaining a maximum value of 30% at 313.2 K. Jha et al. [140] reported that the extraction efficiency of sulfur compounds was slightly increased with the increase in extraction temperature using diglycol-based DESs. Makoś and Boczkaj [131] studied the effect of extraction temperature on the extraction efficiency. The extraction efficiencies were found to increase with the increase in temperature from 293.2 K to 313.2 K; however, a further increase in temperature (313.2 K to 343.2 K) resulted in the reduction of extraction efficiency. Using TBAC/propionate (1:2) and TBAC/PEG (1:2) DESs, high extraction efficiency of around 71% of sulfur content was achieved, and equilibrium was reached in only 10 min. The viscosity of a solvent plays an important role in reaching equilibrium; i.e., a shorter equilibrium time would be achieved with lower solvent viscosity and higher extraction capability.
The LLE method has been widely applied for the removal of sulfur and nitrogen compounds. Hizaddin et al. [141] screened 94 DESs for potential applications in the extractive denitrification of diesel via a conductor-like screening model (COSMO-RS). The extraction efficiency of nitrogen compounds was investigated in terms of capacity, selectivity, and performance index. The screening results showed higher selectivity using ammonium-based DESs but higher capacity using phosphonium-based DESs. Moreover, DESs with amide and alcohols as HBDs resulted in higher selectivity, while DESs with carboxylic acid as the HBD exhibited higher capacity. The effect of molar ratio on the selectivity and capacity was not significant. In another study, the same group [142] compared the performance of two ammonium-and phosphonium-based DESs for the extraction of pyridine, pyrrole, indoline, and quinoline from n-hexadecane. Phosphonium based DES (TBPB/EG, 1:2) was found to have higher selectivity values and distribution ratio than ammonium-based DES toward nitrogen compounds. Hadj-Kali et al. [143] compared the performance of four DESs for the removal of sulfur compounds (thiophene) from n-heptane. The four systems are compared in a ternary diagram, as shown in Figure 12. The DES based on sulfolane (Sulf) as an HBD (TBAB/Sulf, 1:7) showed higher extraction efficiency of up to 35%. The extraction efficiency of sulfur compounds depends on the alkyl-chain length of the HBA; for example, the DES with longer alkyl chain length on the HBA had a higher thiophene distribution capacity. Warrag et al. [128] found very high selectivity (higher than that of ILs and DESs) for thiophene using TEAC/gly (1:2) DES but the distribution capacity was lower using the same glycerol but DESs. When glycerol was replaced with EG in the DES, higher distribution coefficient was achieved compared to glycerol-based DES owing to the higher thiophene solubility in the EG-based DES. Alli and Kroon [8] studied the LLE of a compound consisting of both sulfur and nitrogen compounds (benzothiazole) via tetrahexylammonium bromide (THAB)-based DESs. THAB/EG (1:2) exhibited a higher (greater than unity) selectivity and distribution ratio for the extraction of benzothiazole from n-heptane. THAB/EG (1:2) was also used for the removal of a sulfur compound (thiophene) from n-hexane and n-octane. Both selectivity and distribution ratio were lower for thiophene (compared to benzothiazole) [127]. Various DESs used for the removal of sulfur and nitrogen compounds, along with their selectivity and distribution ratio, are presented in Table 5.

Conclusions
In this study, the use of DESs as green solvents for the capture of CO 2 , SOx, NOx, and NH 3 gases was critically reviewed. We found that both components of the DESs play an important role in determining the solubility of these gases in the reported DESs. As expected, an increase in pressure and decrease in temperature increased the solubility of the gases in the DESs. However, the magnitude of enhancement varied depending on the type of components in the DESs. The highest CO 2 absorption was in the amine-based DESs with a maximum value of 2.7 mol·kg −1 for ChCl/MEA (1:7) exceeding that in aqueous MEA. However, the solubility of CO 2 depended strongly on the HBA and the range was from 0.338-2.700 mol·kg −1 . In addition, it was found that both physical and chemical absorption of CO 2 contribute to the solubility in amine-based DESs. The physical absorption will reduce the regeneration energy significantly. It is worth noting that not all amine based DESs had high CO 2 solubility. The presence of water in the DESs affected the solubility of CO 2 in most of the cases. Hence, it is of great importance to report the water content in DESs. Unfortunately, this was not done in many publications. It was found that the solubility of SO 2 in DESs is comparable to that in ILs with a maximum of 1.54 g SO 2 /g DES for KSCN/caprolactam (1:3). For NO, the maximum solubility was 4.1 mol NO/mol DES for TBPC/DMTU (1:3) at 0.1 MPa and 303.2 K. The data for the solubility of NO 2 in DES was scarce. The maximum solubility of NO 2 was 0.551 mol NO 2 /mol DES at 298.2 K in ChCl/EG (1:2). Several DESs gave promising results for the absorption of NH 3 . The solubility of NH 3 in ChCl/tetrazole/EG (3:7:14), ChCl/LV (1:4), and EaCl/phenol (1:7) was 9.952, 9.494, and 9.801 mol·kg −1 , respectively. In all cases, the presence of water affected the solubility of gases in the DESs. It could be easily noted that a great effort is still needed to find a DES that can be used for the absorption of all acid gases discussed in this review.
Some reports indicated that the molar ratio of the components of the DES affected its ability to absorb the gases; however, other reports indicated that there are no significant changes in solubility with changes in the molar ratio. This could be attributed to the different chemical structure of the components of the DESs. Several methods, e.g., Redlich-Kwong and Peng-Robinson equation of state, were used to correlate the experimental data, and good agreement between the calculated and experimental results was achieved in most cases. Values of Henry's law constant were calculated and reported for several DESs. In addition, COSMO-RS was used to predict the solubility of CO 2 in some DESs. One important factor that was not given proper attention in the reported studies is the regeneration energy that is needed for the release of the dissolved gas from the DES. Moreover, the effect of the presence of more than one gas in the feed on the separation process must be investigated. However, it is clear that, except in the case of CO 2 , more work is still needed to understand the effect of different parameters on the solubility of SOx, NOx, and NH 3 gases in DESs. In addition, more robust thermodynamic models for both correlating and predicting the solubility of these gases in different DESs must be tested. For CO 2 , pilot plant experiments should be performed in order to move toward commercial utilization of the selected DESs in the capture of CO 2 under different operating conditions. In a parallel of this step, simulations using commercially available packages should be used to determine the optimum operational conditions of the process.