Article in HTML

Author(s): Benvikram Barman, Manoj Kumar Banjare, Bhupendra Singh Banjare, Dolly Baghel

Email(s): benvikrambarman2@gmail.com , manojbanjare7@gmail.com , bhupendra0889@gmail.com , dolly54us@gmail.com.

Address: Department of Chemistry, Govt. Naveen College Thelkadih, Khairagarh-Chhuikhadan-Gandai, (C.G.), 491444, India.
Chemistry Division, State Forensic Science Laboratory, Tikrapara, Pujari Park, Raipur, CG, 492001, India.
Department of Chemistry, Nayak Nityanand Sai Govt. College Aara, Jashpur, CG, 496331, India.
MATS School of Sciences, MATS University, Pagaria Complex, Pandri, Raipur (C.G.), 492004, India.
*Coresponding Author: manojbanjare7@gmail.com
manojbanjarechem111@gmail.com

Published In:   Volume - 38,      Issue - 1,     Year - 2025


Cite this article:
Barman, Banjare, Banjare, and Baghel (2025). Deep Eutectic Solvents in Green Chemistry: A Review. Journal of Ravishankar University (Part-B: Science), 38(1), pp. 90-128. DOI:



Deep Eutectic Solvents in Green Chemistry: A Review

Benvikram Barmana, Manoj Kumar Banjareb*, Bhupendra Singh Banjarec and Dolly Bagheld

aDepartment of Chemistry, Govt. Naveen College Thelkadih, Khairagarh-Chhuikhadan-Gandai, (C.G.), 491444, India.

   bChemistry Division, State Forensic Science Laboratory, Tikrapara, Pujari Park, Raipur, CG, 492001, India.

cDepartment of Chemistry, Nayak Nityanand Sai Govt. College Aara, Jashpur, CG, 496331, India.

dMATS School of Sciences, MATS University, Pagaria Complex, Pandri, Raipur (C.G.), 492004, India.

benvikrambarman2@gmail.com, manojbanjare7@gmail.com,  bhupendra0889@gmail.com, dolly54us@gmail.com.

Abstract

Deep eutectic solvents (DESs) as green solvents and sustainable solvents used as replacements for traditional organic solvents and highly applicable for various purposes due to their good chemical properties, such as depression freezing point, low volatility, being biofriendly in nature, less toxicity, environmental friendliness, non-toxic nature, ability to be recycled, reusability, biodegradability, nontoxicity, low vapour pressure, low flammability, etc. These unique physicochemical properties make them perfect for applications in extraction, catalysts, electrochemistry, biotransformation, extracting bioactive compounds, as a green solvent, for nanomaterial synthesis, for metal extraction, for drug delivery, for gas capture, for therapeutic applications, etc. In this paper review, study their method of preparation, types of DESs and its significance in various fields, along with their salient physicochemical properties. DESs can be synthesised by the mixing of hydrogen bond donor (HBD) and hydrogen bond acceptor (HBA) chemical molecules with the proper ratio and heating them.   Synthesised DESs It’s characterised by spectroscopic techniques such as Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance spectroscopy (NMR) techniques, etc. Future research directions are also covered, along with some issues. This analysis offers insights into DES's function in promoting sustainable chemical processes by critically assessing its potential in green chemistry.

Keywords: Deep Eutectic Solvents, Green Chemistry, Sustainable Solvents, Ionic Liquids, Catalysis, Biodegradability.

1.   Introduction

Green chemistry has become a guiding principle for designing environmentally benign and efficient chemical systems as a result of the growing global concern over environmental pollution and resource depletion [1-5]. One of the most popular substitutes for hazardous chemical solvents is DESs. DESs are cleaner, safer, and more sustainable. These are solvent combinations, or interactions, involving a variety of compounds that are joined by van der Waals forces and hydrogen bonds. Consequently, the melting points of DESs are lower than each individual component melting point of DESs due to the strong hydrogen bonding and interactions between components in a DES disrupt the crystal lattice of the pure substances then get lower eutectic melting point [6-7].  The majority of these substances and some key physicochemical characteristics of DESs that make them attractive for green chemistry due to their good chemical properties, such as a depressed freezing point, low volatility, being biofriendly in nature, less toxicity, environmental friendliness, non-toxic nature, the ability to be recycled, reusability, biodegradability, low vapour pressure, low flammability, etc. When two or more substances are combined to create a eutectic system [8-10].   These solvents, which are typically composed of an HBD and an HBA in specific molar ratios and at the proper temperatures, use hydrogen bonding to create a stable liquid phase at room temperature or slightly above it. Deep eutectic solvents (DESs) are molten salts. This new family of green solvents has garnered a lot of attention nowadays in the field of ecological analytical chemicals.   Green solvents and sustainable solvents used as replacements for traditional organic solvents and highly applicable for various purposes. It has favourable qualities such as being inexpensive, industrial, biocompatible, and biodegradable. These advantages have led to the widespread use of DESs in place of conventional organic solvents for the extraction and pre-concentration of a variety of inorganic and organic chemicals. DES which were first presented by Abbott et al. in 2003, are comparable to ionic liquids (ILs) and he got are frequently less costly, simpler to make, and more ecologically friendly and its adjustable characteristics. DES have been used in a number of industries, such as biomass processing, electrochemistry, extraction, pharmaceuticals, and catalysis, etc. [11-13]. The function of DESs in green chemistry is thoroughly examined in this review. It examines the basic ideas underlying their creation, important physicochemical characteristics, and their benefits over ionic liquids and traditional solvents [14-20]. DESs have garnered a lot of interest from scientists worldwide. Recent developments in DES applications for environmentally friendly chemical processes are also covered, as well as present difficulties, potential avenues for further study and highlighting its potential [21-25]. This study aims to promote continuing work towards more ecologically friendly and sustainable chemical techniques [26–30]. Another name for DESs is “inexpensive substitutes for ionic liquids”. This family of newly developed solvents is being used in a variety of novel analytical techniques that are less damaging to the environment than traditional processes that rely on dangerous organic solvents [31-43].

2.    Review of Literature

Barman et. al. (2024), Analyse the micellar behaviours of the three synthesised DESs combined with sodium dodecyl sulphate (SDS) using a range of methods, such as UV-viz spectroscopy, FTIR, surface tension, viscosity, and fluorescence. Choline chloride and amino acids 2:1M are combined to generate DESs, which are further characterised using the FTIR technique and their colloidal properties investigated. Depending on their concentration, three different DESs at 5 and 10 weight percent interact differently with SDS micellar properties [44].

Tang et. al. (2023), discovered that combining CTAB with lactic acid (LA), a DES intended to improve the enzymatic digestion efficiency of rice husk (RH). The findings show that xylan and lagnin are being removed by a mixture of lactic acid and DES CTAB, and that RH is being treated by the enzymatic hydrolysis activity of LA and CTAB. Because of the overall decline in lignin surface area and hydrophobicity, more functional DESs could be encouraged by biorefinery pretreatment [45].  

Banjare, R. K. et al (2020) Analyse the aggregation of surfactants in aqueous demineral solutions, such as cetyldimethylethanolammonium bromide (CDMEAB) and cetyltributylphosphonium bromide (CTBPB). Synthesis DESs are characterised using a range of spectroscopic techniques, whereas CMC is examined using DLS, conductivity, surface tension, fluorescence, and other methods. The best colloidal systems are created with this combination [46].

Banjare R.K. et. al, (2021), Examine the micellisation behaviour of "Tetradecyltrimethylammonium bromide (TTAB) and CTAB" in DESs solutions. ChCl: urea/ethylene glycol (EG) is combined in a 1:2 mol ratio to create DESs, which are then characterised using the FTIR method. This interaction causes the systems' critical micelle concentration (CMC) to decrease and their aggregation number to increase. Significantly, the data indicates that surfactant containing DESs prefers micellar behaviour. this research condut bu the using of Conductivity, UV-visible spectroscopy, dynamic light scattering (DLS), and other techniques [47].

Ghosh et al., (2018), studies the FT-IR, UV-vis, DLS, and fluorescence spectroscopy techniques were used to examine the aggregation behaviour of the short-chain IL [Bmim][OS] inside aqueous DESs. By heating choline chloride, an ammonium salt, with either HBD urea or glycerol in a 1:1:2 molar ratio, we have synthesised two DESs, ChCl-urea and ChCl-Gly. A significant decrease in the CMC and an increase in the aggregation number (Nagg) are seen when DES solutions are contrasted with water, indicating that the micellisation process of the IL [Bmim][OS] is significantly more advantageous in DES solutions. The molecular interactions of [Bmim][OS] in DESs are clarified by the use of FT-IR spectroscopy. Additionally, these methods were used to study the IL-drug binding of the antidepressant promazine hydrochloride (PH) [48].

Xu et al., (2017), study the basic properties of DESs, specifically their biodegradability and toxicity. Additionally, it illustrates the several beneficial applications of DES as a co-solvent and solvent in biocatalytic processes, such as lipase-catalyzed transesterification and ester hydrolysis reactions [49].

Bajkacz et al.,(2020) examined the ability and effectiveness of DESs to extract seven catechins from various tea varieties. Different combinations of DES were used. Malic acid was present in DES as the HBDs showed a high solubility of catechins with different polarities. In the second part of the investigation, the SPE technique was used to extract catechins from tea infusions. This method was used to identify specific catechins in tea leaves and infusions. Furthermore, we demonstrated that the recommended approach is an effective tool for tea quality control as it works well for the simultaneous monitoring of these polyphenols [50].

Pauli et al., (2018), discussed the NADES-related observations in NP research and reports application of their EM. investigated the focusses on NADES properties and applications in NP research with the aid of consecutive and statistical investigation of existing reports and recognition of the distinctiveness of NADESs [51].

Pinho et. al. (2024), study physicochemical properties of choline and organic acid based DESs. Spectroscopic techniques used to conformation of carboxylic esterification reaction specific malonic acid mixture and thermal analysis include differential scanning calorimetry and thermogravimetric analysis. He found that thermophysical behaviors of DES are described by linear relationships, where the size of the alkyl chain exerts a considerable influence on the parameters of density, viscosity, and refractive index [52]. 

Liu et al., (2016),  examined the evaluation of DESs for bioactive natural substance extraction. Analyse the potential for extracting different natural chemicals from biomass using DESs. To assess how well DESs extracted flavonoids, alkaloids, saponins, phenolic acids, and anthraquinones, in that order, Chinese herbal remedies were selected [53].

Fernandez et al.,(2017), studied the self-assembly of alkyl trimethylammonium bromide surfactants in ChCl: water, solvent combinations, and malonic acid DES. The behaviour of the amphiphiles was examined using surface tension and small-angle neutron scattering. The formation of stretched micelles is explained by the solvent's interaction with the surfactant head group [54].

Campos et. al. (2024), analysis outlines the primary uses of DESs that are in line with the 2030 Agenda for Sustainable Development of the United Nations, particularly those pertaining to improving energy efficiency, sustainable industrial practices, and climate change mitigation. An introduction of the use of DESs for process intensification and sustainable production is provided [55].

Dlugosz et. al. (2024), DES can be obtained in large scale, which will facilitate of these important solvents. Using ultrasound and microwave radiation as energy sources for mix them. it was established that using alternate energy sources to obtain processes is achievable if the process is well designed and only depends on DES raw materials and products [56].

Dlugosz et al., (2023), examine the deep eutectic solvents found in nature for the creation of inorganic nanoparticles. including the extraction process sector as well as the domains of separations, gas capture, metallurgy, biocatalysis, nanotechnology, and electrodeposition. They are utilised in many different industrial areas because to their qualities, which include ease of preparation, environmental friendliness, biocompatibility, and multifunctionality [57].

Prandi et al., (2023), study the advantages of using DESs to promote organic processes in addition to their many other uses. In biocatalyzed processes, eutectic mixtures have been reported to be employed as reaction media, providing enhancements in sustainability and selectivity [58].

3.   Classification of DES

DES can be classified into different categories based on their composition and the nature of the interactions between their constituents. The most commonly used classification is the one proposed by Smith et al. (2014) [59], which divides DES into four main types:

Table 1. DES categorisation examples and a general formula

S.N.

Types of DESs

DESs components

Formula

Terms

Examples

1.

DES-I

Quaternary salts + anhydrous metal chloride

Cat+ X- zMClx

M=Zn, Sn, Fe, Al, Ga, In

Choline chloride (ChCl) + ZnCl2

2.

DES-II

Quaternary salts + hydrated metal chloride

Cat+ X- zMClx. y H2O

M= Cr, Co, Cu, Ni, Fe

Choline chloride + CoCl2.6H2O

3.

DES-III

Quaternary salts + HBD compounds

Cat+ X- zRZ

Z=OH, COOH, CONH2

ChCl+ Urea

4.

DES-IV

Metal chloride + HBD compounds  

MClx +RZ = MCl+x-1 RZ + MCl x+1

M= Al, Zn, and Z= OH,

 

Urea +ZnCl2

 

3.1.  Type I DESs (Metal Salt-based DESs)

Type I DESs are created by mixing metal salts, such as metal chlorides, with HBD, such as urea or ethylene glycol. made up of a quaternary ammonium salt (such as choline chloride) and a metal chloride (such as AlCl₃, ZnCl₂, and FeCl₃). These DESs are frequently employed in metal processing, electrochemistry, and catalysis due to their strong ionic conductivity. For instance, choline chloride and AlCl₃ combine to generate a DES that has a lower melting point than either substance alone. These may break down when exposed to water because they are moisture-sensitive.

3.2.  Type II DESs (Hydrated Metal Salt-based DESs)

Produced by mixing metal salts, such as metal chlorides, with HBD, such as urea or ethylene glycol. Though they contain hydrated metal salts (such as ZnCl₂·xH₂O and FeCl₃·6H₂O), they are comparable to Type I. Ionic interactions are altered by the presence of water, which makes them more stable and adjustable for certain uses. utilised in the processes of separation, electroplating, and metal extraction.

Example: ZnCl₂·xH₂O + choline chloride forms a stable DES for metal dissolution.

3.3.  Type III DESs (Organic DESs)

Composed up of a HBD, such as urea, glycerol, ethylene glycol, or carboxylic acids, and a HBA, usually a quaternary ammonium salt (such as ChCl) [60].  The most popular and extensively researched DESs because of their ease of manufacture, biodegradability, and non-toxicity [61]. utilised in biomass processing, medication solubilisation, pharmaceuticals, and enzyme stabilisation [62].

Example: Choline chloride + urea (1:2), a widely used DES for solubilizing biomolecules.

3.4.  Type IV DESs (Metal-containing DESs)

Produced by strong hydrogen bonding between non-ionic species, such as neutral molecular compounds. made up of metal salts, which are complexes created when metal ions interact with organic ligands [63]. frequently employed in the production of nanomaterials, polymer synthesis, and catalysis. can be modified for certain metal-focused uses, like metal recovery or electrocatalysis [64-65].

Example: Transition metal salts + urea or ethylene glycol to form a DES used in metal deposition. Every variety of DES has unique physicochemical characteristics that enable it to be used in a wide range of processes, from biomass valorisation to medicinal formulations and metal processing.

4.   Methods of Preparation

A quaternary ammonium salt (QASs) can be converted into a DESs by combining it with a HBD or metal salts that have the ability to combine with the halide anion of QASs to create a complex [66]. The combination has a lower freezing point (Tf) than its constituent parts due to charge delocalisation brought on by hydrogen bonding (HB) between the halide ion and later the hydrogen-donor (HD) moiety [67-68]. The substance Choline chloride (ChCl) is most frequently used to create DESs [69-70]. Easily synthesised from fossil deposits (million metric tonnes) or recovered from biomass [71-74]. It is reasonably priced, non-toxic, biodegradable, and environmentally safe [75]. A DES can be produced when ChCl aggregates with safe HBD like renewable carboxylic acids, urea (citric acid, succinic acid, oxalic acid, or amino acids), or renewable polyols (polysaccharides, glycerol). Synthesis of deep eutectic solvents show in Fig.1. and HBDs: HBAs molecules show in fig.2. its characterised by NMR and FTIR techniques [76-80].

Figure 1. Preparation process of amino acids based DESs 


Figure 2. The chemical structure of halide salts and hydrogen bond donors


5.    Physicochemical Properties

The unique properties of DES contribute to their growing significance in green chemistry. DESs are made by combining various HBD and various quaternary ammonium salts (QASs), including ChCl. Conductivity, pH, viscosity, surface tension, phase behaviour, and freezing point are some of the physicochemical properties of DESs [81-85]. DESs physicochemical characteristics will be examined in this section [86]. Table 2 show the temperatures of freezing point on a variety of DESs [87]. Sustainable technologies used in green-related material science applications should be crucial in the ensuing decades [88]. Ionic liquids (ILs) may be replaced with deep eutectic solvents (DESs), which keep the majority of important characteristics like task-specific character show in fig.3 [89-90]. Some of the key physicochemical characteristics of DES include:


5.1.  Tunability

DESs are highly adjustable, their characteristics can be altered by varying the kind and proportion of hydrogen bond acceptors (HBA) and donors (HBD). Properties such as conductivity, hydrophobicity, polarity, and viscosity can be tailored for particular uses by choosing alternative constituents [91]. Because of their adaptability, DESs can be tailored for use in electrochemical, drug delivery, catalysis, and extraction processes [92].

5.2.  High Solubility

Numerous substances, including organic, inorganic, and polymeric materials, can be dissolved by DESs [93]. They are helpful in chemical synthesis, metal extraction, and biocatalysis because of their capacity to dissolve metal oxides, biomolecules, and medications. While hydrophobic DESs are helpful for non-polar extractions, hydrophilic DESs are good at dissolving polar substances [94].

5.3.  Thermal and Electrochemical Stability

DESs are appropriate for high-temperature procedures because of their good thermal stability and frequent decomposition temperatures above 200°C [95]. They can be utilised in batteries, supercapacitors, and electrodeposition because of their broad electrochemical windows (up to 4–5V). Different DESs have different levels of stability; some can break down in the presence of high pH or extended heating [96].

5.4.  Biodegradability and Low Toxicity

Natural, biodegradable, and non-toxic substances like glycerol, urea, and choline chloride are frequently used to make DESs [102]. DESs are safer for biological applications and less harmful to the environment than conventional ionic liquids and organic solvents. They are appropriate for use in food, medicine, and pharmaceuticals due to their biocompatibility [103].

5.5.  High Viscosity

The comparatively high viscosity of DES is a significant disadvantage that could restrict its diffusion qualities in specific applications [104-105]. However, by altering the hydrogen bonding network or introducing co-solvents, viscosity can be maximised [106]. It is necessary to consider the viscosity of the DESs. Except for the eutectic mixture (EM) of ChCl and (CH2OH)2, most DESs have quite high viscosities (>100 cP) at room temperature. It is often assumed that the high viscosity of DESs, which results in a reduced mobility of free species inside the DESs, is caused by the development of a dense hydrogen bond network between each component. DESs are characterised by large ion sizes and small void volumes, and their high viscosity may also be a result of electrostatic or van der Waals interactions [107]. The viscosity (η) of eutectic mixtures is influenced by the kind of NH4+ salts and HBDs present, their molar ratio with organic salts, other chemical properties, temperature, and water content, among other things. Van der Waals interactions, hydrogen bonds, and electrostatic interactions all have an impact on the viscosity of binary eutectic mixtures. The HBD used to determines the viscosity of the ChCl – DESs [108].

 



Table 2. Temperatures of freezing point on a variety of DESs

S.N.

Halide salt

Mp (°C)

HBD

Mp (°C)

Salt: HBD (molar ratio)

Tf (°C) of DES

Ref.

1.

ChCl

303

Adipic acid

153

1:1

85

97

2.

ChCl

303

1,3-dimethyl urea

102

1:2

70

98

3.

ChCl

303

1,1-dimethyl urea

180

1:2

149

98

4.

ChCl

303

1-methyl urea

93

1:2

29

98

5.

ChCl

303

Acetamide

80

1:2

51

98

6.

ChCl

303

Banzamide

129

1:2

92

98

7.

Methyltriphenylphosphonium Bromide

231−233

Glycerol

17.8

 

- 4.03

99

8.

Methyltriphenylphosphonium Bromide

231−233

Ethylene glycol

−12.9

 

- 49.34

99

9.

Methyltriphenylphosphonium Bromide

231−233

2,2,2-trifluoro acetamide

73−75

 

−69.29

99

10.

Methyltriphenylphosphonium Bromide

231−233

Glycerol

17.8

 

- 4.03

99

11.

Methyltriphenylphosphonium Bromide

345−347

Glycerol

17.8

 

50.36

99

12.

ZnCl2

293

Urea

134

 

9

99

13.

ZnCl2

293

Ethylene glycol

-12.9

 

-30

99

14.

ZnCl2

293

Hexanediol

42

 

-23

100 -101


5.6.  Green credentials

DESs are safer, cleaner, and more sustainable. DESs could provide a "greener" substitute for a number of conventional ILs and the unique properties of DESs are responsible for widely significant compare to other ILs basis environmental impact, such as a, non-flammability, less toxicity, recyclable, environmentally friendly and biodegradability etc, green tools of DESs show in scheme 1.4 and scheme 1.5 [109-110].

5.7.  Ionic conductivity

Most DESs have weak ionic conductivities due to their relatively high viscosities (lower than 2 mS cm-1 at room temperature). As conductivity declines, viscosity rises [111]. The conductivities of DESs frequently increase with temperature because the viscosity of the DESs decreases. Changes in the organic salt/ HBD molar ratio clearly have a large effect on DES conductivities because they also have a considerable impact on DES viscosities [112].These unique properties make DESs highly valuable in green chemistry, energy storage, pharmaceuticals, and industrial applications [113-117].

Table 3. Physical properties of DESs and molecular solvents at 298 K Salt

S.N.

Salt

HBD

Molar ratio

Viscosity (cp)

Conductivity (ms cm−1)

Density/gc

(m−3)

Surface tension (mNm−1)

1.

ChCl

Glycerol

1:3

450

1.05

1.20

50.8

2.

ZnCl2

Urea

1:3.5

11 340

0.18

1.63

72

3.

ZnCl2

Acetamide

1 : 4

 

 

1.36

53

4.

C4mimCl

AlCl3

 

19

9.2

1.33

 

5.

ChCl

CF3CONH2

1:2

 

0.286

1.342

 

6.

ChCl

Ethylene glycol

1:3

19

 

1.12

45.4

 

5.8.  Surface tension

The energy needed to raise the surface area per unit area is known as surface tension, and it is produced at the contact by intermolecular forces [118]. Surface tension is a basic fluid feature. It is affected by temperature and the strength of DES intermolecular contacts [119], and it affects the effect of DES in mass transfer interfacial processes [120]. Most DESs have a surface tension that is greater than that of traditional solvents [121]. The interactions between HBD and HBA have a considerable impact on the DES surface tension. The surface tension of DESs is influenced by the strength of the connections between HBD and HBA [122]. Together with a comparison to ionic liquids that include discrete anions and specific molecular solvents, Table 2 provides a few instances of physical properties for a number of DES types at the eutectic composition at 298 K. In contrast to other ionic liquids (ILs) and molecular solvents, DESs have relatively high viscosities and low conductivities. The large ion sizes and relatively free space in the ionic systems are thought to be the reason of this discrepancy. The high ion sizes and comparatively huge free volume in the ionic systems have been blamed for this discrepancy. ILs have viscosities that are significantly higher than those of the most widely used molecular solvents. It shows that the viscosity has an Arrhenius trend with temperature and that the activation energy of viscous flow has a wide range of values.

5.9.  Phase changes in behavior

The difference, ΔTf, between the freezing point at the eutectic composition of a binary mixture of A and B and that of a theoretical ideal mixture is independent of the degree of interaction between A and B. The more the interaction, the greater the ΔTf. Figure 4 depicts this schematically. Let's start with eutectics of type I: The quaternary ammonium salt's halide anion will interact with various metal halides to form identical halometallate classes with comparable enthalpies of formation. Therefore, ΔTf values should fall between 200 and 300 °C. It has been found that a metal halide's melting point frequently has to be 300 °C or lower in order for a eutectic to form at room temperature. Therefore, it is easy to comprehend why eutectics are produced at room temperature by metal halides such as FeCl3 (308) [123], AlCl3 (mp=193°C) [124], SnCl2 (247) [124], ZnCl2 (290) [125], InCl3 (586) [126], CuCl (423) [127], and GaCl3 (78) [128]. Metal salts such as SbCl3 (mp = 73°C), BeCl2 (415), BiCl3 (315), PbBr2 (371), HgCl2 (277), and TeCl2 (208) may also be predicted to create ambient temperature eutectics, but they have not yet been investigated.

 


Figure 4. Diagrammatic illustration of a two-component phase diagram's eutectic point

 

On the other hand, reduced melting point Because quaternary ammonium compounds have a lower melting point due to fewer symmetrical cations, they are eutectic. To add more metals to the DES formulations, type II eutectics were created. It was discovered that the melting point of the associated anhydrous salt was greater than that of metal halide hydrates. It is clear that by reducing the lattice energy, the waters of hydration lower the melting point of metal salts. As shown in Fig. 4, a lower melting point of the pure metal salt (ΔTf) will lead to a smaller depression of the freezing point (ΔTf). The eutectic point concept explains the physical properties of DESs at the eutectic composition; the mixture forms a homogeneous liquid with the lowest melting point due to maximal disruption of crystal structures through intermolecular interactions like hydrogen bonding [129].

6.   Comparison of DES with conventional solvents and ionic liquids

Green chemistry has seen a surge in interest due to the introduction of Deep Eutectic Solvents (DESs) as a substitute for traditional solvents and Ionic Liquids (ILs). DESs are very promising for environmentally friendly, less toxic, biodegradable, non-volatile, and it is made from biomolecules etc. since they have distinct advantages over both conventional organic solvents and ILs. A comparative study of DES is presented in this section, emphasising both its advantages and disadvantages [130]. DESs be considered a more sustainable option than ionic liquids, even though both are alternatives to organic solvents DESs are typically made from cheap, abundant, and biodegradable components (e.g., choline chloride, urea), unlike many ILs, which are expensive, less biodegradable, and may have toxicity concerns. DESs support green chemistry principles in terms of synthesis and disposal better than conventional solvents based on easy preparation, mild reaction conditions, recyclability, and low environmental persistence and reduced hazardous waste generation [131].

6.1.  Advantages of DES over traditional organic solvents

Chemical synthesis, extraction, and industrial applications have made extensive use of traditional organic solvents like benzene, acetone, methanol, and dichloromethane. They frequently have toxicity, volatility, and environmental persistence, though, which raises major ecological and health issues. DESs are often easier to synthesize, and more scalable, with less regulatory and toxicity concern compared to ionic liquids, making them better suited for industrial use [132].

6.2 Low toxicity and biodegradability

Since many DES are made of naturally occurring substances (such as glycerol, urea, and choline chloride), they are naturally less hazardous and biodegradable than solvents derived from petroleum.

DESs are typically non-toxic and biodegradable, in contrast to many conventional organic solvents (such as acetone, benzene, and chloroform), which can be dangerous and persistent in the environment [133]. The environmental impact of many DESs is decreased because they are made from natural, environmentally beneficial ingredients such choline chloride, urea, glycerol, and amino acids. They are safer for use in laboratories and industries because of their low volatility, which reduces exposure dangers and air pollution. DESs are favoured in applications including food processing, cosmetics, and medicines where toxicity is an issue because to their biocompatibility [134].

6.2.  Non-volatile nature

The DES their low vapour pressure, in contrast to volatile organic solvents (VOCs), minimises air pollution and lowers the chance of being exposed to dangerous vapours. DESs are special solvents due to its melting point low compare to its individual components.  DESs are non-volatile in contrast to conventional organic solvents (such as ethanol, acetone, and chloroform), which have high vapour pressures and evaporate readily [135]. It’s very safer useful in industrial and laboratory chemical due to it is a environmentally friendly this properties make its special, decrease the health hazardous.  DESs are perfect for extraction procedures, high-temperature applications, and the production of eco-friendly chemicals. They serve as sustainable green solvents in part because they are non-volatile [136].

6.3.  Non- flammability

DESs of their strong ionic connections and low vapour pressure, DESs are naturally non-flammable, in contrast to many conventional organic solvents (such as ethanol, acetone, and ether), which are extremely flammable [137]. Due to this characteristic, they are safe to use in large-scale chemical reactions, laboratories and industrial processes, reducing the risk of fire. their stability at high temperatures, they are suitable for metal processing, electrochemistry and thermal applications. Because non-flammability removes the need for additional safety measures required for volatile organic solvents, it also improves storage and transportation safety. this characteristic, DES are a safe choice in sustainable and green chemistry [138].

6.4.  Enhanced solubility

DES are suitable for catalytic and extraction applications due to their special solving unique power for a wide variety of substances, such as metal oxides, biopolymers and drugs. for a wide variety of chemicals, including organic, inorganic and polymer materials, DESs show exceptional solubility. They are more effective than many conventional solvents at dissolving metal oxides, proteins, carbohydrates and drugs [139]. They work well for metal extraction, pharmaceutical manufacturing, and biomass processing because of their ability to interact with solutes and break hydrogen bonds. By some modification in their structure of DESs the HBD and HBA, DES can be made to dissolve particular molecules in the way [140].

6.5.  Easy and low-cost preparation

DES is formed by combination a HBD and a HBA, often under moderate circumstances with just heating and stirring [141]. DES may be formed without costly reagents or dangerous methods. Because DES are composed of glycerol, urea, and choline chloride, they are frequently inexpensive, readily available, and biodegradable. Their practical significance is further enhanced by the ease of preparation which enables adaptation to particular industrial or laboratory requirements. Because of this, DES are a desirable, cost-effective, and environmentally friendly they alternative to traditional solvents such as ionic liquids [142].

7.   Differences between DES and ILs

Ionic Liquids (ILs) have been extensively researched as environmentally friendly solvents because of their great thermal stability, tunability, and low volatility [143-149]. In some cases DESs are similar to ILs Both are low-melting-point liquids, often composed of ionic or hydrogen-bonding species, and are used as green alternatives to volatile organic solvents. They share low vapor pressure, tunability, and chemical stability [150-151]. DES, however, have a number of unique benefits that increase their attractiveness for applications involving green chemistry (Table 4) [152].

Table 4. A systematic representation of difference between DES and ILs

Property

Deep Eutectic Solvents (DES)

Ionic Liquids (ILs)

Composition

Mixture of a HBA and a HBD.

Pure salts composed entirely of cations and anions.

Synthesis

Simple, prepared by mixing and heating components without chemical reactions.

Often requires complex synthesis and purification steps.

Volatility

Non-volatile due to strong hydrogen bonding.

Also non-volatile but some ILs may degrade at high temperatures.

Cost

Low-cost, made from readily available and biodegradable materials.

Expensive due to specialized synthesis and purification processes.

Toxicity & Biodegradability

Generally non-toxic and biodegradable (e.g., choline chloride-based DESs).

Some ILs are toxic and non-biodegradable, though newer bio-ILs exist.

Viscosity

Generally higher viscosity, but tunable by composition.

Can have lower viscosity depending on the ionic structure.

Stability

Can degrade under extreme conditions (e.g., high moisture, strong acids/bases).

Typically, more thermally stable, but some decompose at high temperatures.

Environmental Impact

Considered greener and more sustainable.

Some ILs pose environmental concerns due to toxicity and poor biodegradability.

Electrochemical Properties

Moderate electrochemical stability, suitable for some applications.

High electrochemical stability, widely used in batteries and electrochemistry.

Solubility

Can dissolve a wide range of substances (organic, inorganic, and biomolecules).

High solubility but varies depending on the cation-anion combination.

 

8.   Applications of DES in green chemistry

DESs in green chemistry because of its exceptional solubility qualities, cheap cost, non-toxic, and biodegradable components, and ecologically friendly character, Deep Eutectic Solvents (DESs) are becoming more and more popular in the field of green chemistry [153]. These solvents are very appealing in a variety of chemical processes, especially those that adhere to the sustainable development principles, because they provide an environmentally benign substitute for conventional organic solvents and ionic liquids [154]. The use of DESs in synthesis, extraction, catalysis, biochemistry, and environmental applications will be the main topics of this article's discussion of green chemistry applications. Some challenges during facing when use of DESs such as high viscosity, Limited data on long-term toxicity, Water sensitivity of some formulations (hygroscopicity), Lack of standardization eg. naming, classifying, benchmark DESs [155].

8.1.  Extraction and separation processes

Organic solvents that are poisonous, combustible, and non-biodegradable are frequently utilised in extraction procedures, particularly those used in waste treatment, metal recovery, and the isolation of natural products [156-157]. Because DESs can extract different molecules from natural sources selectively and with little harm to the environment, they provide a green option for these procedures [158-160].

8.1.1. Liquid-liquid extraction

The use of DESs in liquid-liquid extraction (LLE) is among their most important uses in green chemistry [161-163]. DESs eliminate the need for dangerous organic solvents like hexane or dichloromethane by effectively extracting bioactive substances from plants and natural sources, including essential oils, alkaloids, and polyphenols [164]. DESs provide benefits in terms of extraction efficiency, selectivity, and benign operating conditions [165]. Choline chloride and lactic acid, for instance, have been employed as a DES to extract antioxidants from plant sources [166]. Polar chemicals are selectively extracted by the DES, while non-polar substances are left behind. This characteristic is very helpful for the environmentally friendly extraction of valuable compounds from biomass. DESs compare to other organic compounds e.g. hexane DES different basis such as DESs tunable polarity depending on components but hexane is non-polar DESs consider   green solvent but hexane is volatile and toxic in nature. DESs is non-volatile and hexane is volatile [167].

8.1.2. Metal extraction and recovery

DES are becoming more and more effective solvents for the extraction of metals, especially heavy metals, precious metals, and rare earth elements [168]. Old-style metal extraction methods often involve the use of strong and toxic solvents such as sulfuric or nitric acid, which can produce a lot of waste and be hazardous to the environment [169].  Metals such as copper, nickel and gold have been successfully extracted and recovered DES [170]. These solvents provide a safer and more environmentally friendly alternative to traditional acidic leaching processes by having the ability to selectively dissolve metal salts or complexed metal ions [171]. And also DES has the ability to be recycled and reused, which is increasing process sustainability [172-176].

8.2.  Synthesis of fine chemicals and pharmaceuticals

Green chemistry aims to replace often hazardous solvents and reagents with safer, more environmentally friendly solvents and reagents [177]. DES provides a useful way to synthesize agricultural chemicals, drugs, and fine chemicals [178]. DES are efficient solvents for a variety of chemical reactions, including those that are challenging or impossible to work with conventional solvents due to their broad dissolution spectrum of organic and inorganic molecules [179-180].

8.2.1. Organic synthesis

Because DESs can offer a cleaner, more effective medium for processes including condensation, acylation, and alkylation, their application in organic synthesis is growing [181]. For instance, DESs can take the place of dangerous solvents that are frequently employed in organic reactions, such as benzene, dichloromethane, or chloroform [182]. Because DESs' solubility characteristics are highly adjustable based on the donor and acceptor components, they are very helpful in reactions that call for a polar media [183]. DESs based on choline chloride are frequently employed in the synthesis of organic chemicals, including amides, alkylated products, and esters. ChCl + urea, for example, has been demonstrated to effectively catalyse processes like the esterification of carboxylic acids with alcohols [184]. Particularly efficient in reactions involving biomass and carbohydrates, glycerol-based DESs contribute to the sustainable synthesis of compounds from renewable feedstocks. These reactions become more environmentally benign when DESs are used in place of conventional solvents because they produce less waste, have better atom efficiency, and produce less hazardous byproducts [185].

8.2.2. Pharmaceutical applications

Considering their solubilising properties, non-toxicity, and biodegradability, the pharmaceutical industry has been actively investigating DESs for medication formulation and production [186]. Numerous DESs can function as solvents or excipients in pharmaceutical formulations and solvate poorly soluble medications. Choline chloride + urea DESs, for instance, have been used to make poorly water-soluble chemicals more soluble and hence more accessible [187]. Furthermore, DESs can serve as controlled drug release carriers, providing a more environmentally friendly substitute for the traditional synthetic polymers and solvents frequently used in drug delivery systems [188]. They are especially appealing for use in pharmaceutical processing, such as dissolution research, gel production, and tablet formation, because to their non-volatility and biodegradability [189-190].

8.3.  Catalysis in green chemistry

A important idea in green chemistry is catalysis, which makes it possible for developments to continue more effectively while producing fewer byproducts. Since they can offer a special medium for both homogeneous and heterogeneous catalytic processes [191], DESs have been more and more investigated as solvents in catalysis [192-193].

8.3.1. Homogeneous catalysis

DES has the ability to act as both solvent and catalytic media in homogeneous catalysis [194]. DESs can dissolve reactants, stabilise catalysts, and potentially participate in the reaction process (by serving as proton donors or acceptors), improving reaction efficiency and selectivity. DES are perfectly suited for a variation of catalytic activities, such as esterification, transesterification, and the invention of carbon-carbon bonds, because of the solvent's capability to solvate reactants and promote effective catalytic reactions. For example, choline chloride and urea can be used as a medium in the Friedel–Crafts alkylation reaction to improve reactant solubility and give the catalyst a stable environment [195].

8.3.2. Heterogeneous catalysis

In heterogeneous catalysis, DES are also used to enhance reactions that require a solid-liquid interface or to aid dispersion of the solid catalyst.  DESs they can dissolve both organic and inorganic species while preserving enzyme stability, they are particularly helpful in biocatalysis and enzyme-catalyzed processes [196]. DES are adjustable, it is possible to optimize enzyme activity by adjusting variables such as solvent polarity and viscosity. For example, in enzyme-catalyzed transesterification reactions, choline chloride + urea DES has been employed. In these reactions, DES improves the stability of the enzyme and the solubility of the reactants, thereby increasing yields and reaction rates [197].

8.4.  Biochemical and biomolecular applications

In bioscience DESs used as solvents for DNA extraction, enzymatic fixation etc [198].  These uses provide a bio-compatible and ecologically safe medium for biological reactions, consistent with the ideas of green chemistry [199].

8.4.1. Enzyme stabilization

In various industrial applications, including waste treatment, biocatalysis, and biodiesel production, DES are being used more and more to stabilize enzymes. Because DES can dissolve both polar and non-polar substances, the enzymes can function in a wide range of environments and maintain their stability and activity [200]. For example, choline chloride + urea DES has been demonstrated to preserve the activity of enzymes such as lipase and protease, enabling them to function in processes that would be difficult to accomplish with conventional organic solvents [201].

8.4.2. DNA and RNA extraction

When extracting DNA/RNA from plant and animal cells, DES like choline chloride + glycerol is used [202]. DES are used in genomic extraction because DES are lightweight, nucleic acids (DNA, RNA) can be extracted without degrading or denaturing them. DESs provide a more environmentally friendly alternative to hazardous chemicals such as phenol and chloroform, which are often used in molecular biology laboratories. DESs have several benefits, including improved nucleic acid stability, selective solubility, low toxicity for sensitive biomolecules, and efficient recovery without the use of harmful organic solvents [203].

8.5.  Environmental applications

There is huge potential for environmental purposes. They are helpful in treating industrial waste streams and reducing environmental hazards due to their wide range of solubilizing abilities. its industrial and biochemical applications, DES has applications in waste treatment, pollution prevention, and contaminated site cleanup [204-205].

8.5.1. CO₂ capture

DES such as choline chloride + urea can be used to remove CO₂ from flue gases, providing a green alternative to traditional solvents based on amines. Due to their ability to absorb and decompose CO₂ they can be used to reduce greenhouse gas emissions from industrial processes. DES have been investigated as potential solvents for environmental applications. DESs can be High capacity and recyclability enable selective CO₂ absorption. Effectively dissolve lignocellulosic biomass, allowing for more environmentally friendly biofuel and biochemical synthesis [206-207].

8.5.2. Removal of heavy metals

DES has been used in wastewater treatment to eliminate heavy metals from contaminated water, including lead, mercury and cadmium etc. This hazardous heavy metal can be effectively removed from industrial effluents due to their ability to dissolve and form complexes with metal ions [208-209].

9.   Environmental and economic considerations

DESs have recently attracted much interest due to their special properties and potential use in many fields. Typically created by combining a HBD and HBA these solvents are renowned for their ability to dissolve a wide variety of substances, including biomolecules and both organic and inorganic chemicals DES are therefore often seen as an economically and environmentally suitable alternative to conventional solvents. To properly evaluate their sustainability and feasibility, the impacts of DES on the environment and economy must be carefully considered. The main economic and environmental factors related to DES are given below [210-212]

9.1.  Environmental considerations as a low toxicity and biodegradability

The low toxicity and potential biodegradability of DES are two of its biggest advantages. Due to their low toxicity, DES can be used in biochemical and pharmaceutical applications where biocompatibility and safety are essential DES also used in industrial and laboratory applications, DES is a safe and eco-friendly option. Many conventional solvents, such as dichloromethane, benzene and chloroform, are harmful to both human health and the environment and often require careful handling and disposal. When non-toxic DES are used there are fewer health and environmental problems during manufacturing, storage and disposal because they reduce exposures and contamination hazards [213-215].

9.1.1 Reduced environmental impact

DES are non-volatile and have extremely low vapor pressure, they are often promoted as a more environmentally friendly alternative to traditional organic solvents. This feature greatly reduces the potential for air pollution, often caused by volatile organic compounds (VOCs), which can cause smog and other problems with air quality. DES are more effective than traditional solvents in industrial settings due to their non-volatility, which also results in lower evaporation rates, which reduces solvent loss during chemical reactions. Furthermore, by facilitating more environmentally friendly industrial processes, green solvents like DES have the potential to reduce the overall carbon footprint. For example, its application in CO₂ capture, biomass processing and metal extraction offers the potential to boost recycling and waste reduction while reducing greenhouse gas emissions. By substituting DES for hazardous solvents many processes can be carried out under benign conditions, reducing energy use and hazardous emissions [216-217].

9.1.2   Solubility and waste minimization

DES reducing hazardous waste and increasing recovery yield, this further strengthens their environmental credentials. DES are highly soluble in a wide range of chemicals, allowing them to be employed in clean chemical reactions, reducing waste generation. This characteristic is beneficial in areas where reducing solvent waste can result in financial and environmental savings, such as bioengineering, pharmaceuticals, and precision chemical synthesis. Additionally, DES are often reusable and recyclable, which reduces waste and improves the sustainability of chemical operations. Furthermore, by using DES in extraction processes, valuable compounds can be effectively separated from waste streams or biomass without the use of hazardous solvents [218-219].

9.2.  Economic considerations

9.2.1. Cost-effective synthesis

Low cost of synthesis is one of the main economic recommendations of DES. Traditional solvents often require expensive, complex manufacturing processes that use hazardous chemicals and require a lot of energy. DES, on the other hand, are usually made from inexpensive, easily accessible and renewable materials.  Ex. carboxylic acid, produced using urea, glycerol and choline chloride. Because of this, DES are less expensive to make than many conventional organic solvents, which rely on feedstock derived from petroleum or other specialized raw materials. Furthermore, DESs are generally simple to prepare, requiring only mild heating and mixing. This enables their widespread use in both laboratory and industrial settings by making the preparation process economical and scalable [220- 225].

9.2.2. Reduced operational and disposal costs

DES are non-flammable and have minimal volatility, making them less expensive to handle, store and ship. DES does not require expensive safety precautions, such as ventilation systems or explosion-proof equipment, which are often required for volatile solvents, because they do not provide a major risk of fire or explosion. For industrial facilities using DES on a large scale, this can reduce operating costs. Additionally, DES are often safer and less expensive than traditional solvents, which often require special treatment and disposal methods to reduce their environmental impact, because they are non-toxic and biodegradable. DES can often be recycled and reused, reducing overall solvent management costs [226-227].

9.2.3. Increased process efficiency

In various chemical processes, the improved solubility and selectivity of DES can result in increased yields and accelerated reaction times. For example, DES can increase reaction speeds in metal extraction, biocatalysis, and organic synthesis, resulting in more efficient processes [228-229]. Faster reflexes translate into cheaper operating costs since they demand less time and energy to perform industrial operations. Furthermore, because DESs can dissolve a large variety of chemicals, less reagents and solvents need to be employed, which simplifies production and further reduces costs [230].

10.    Future perspectives and research directions

The promise of DESs as environmentally friendly substitutes for ionic liquids and traditional solvents is demonstrated by their quick rise in popularity in green chemistry [231-232]. But even with their benefits, there are also a number of difficulties. The main research avenues, technical developments, and potential uses of DESs are examined in this section [233-235].

10.1.   Enhancing the physicochemical properties of DES

Optimising the physicochemical features of DES to increase their application is one of the primary research issues in their development [236-237]. Future studies ought to concentrate on:

10.1.1.  Reducing viscosity

High viscosity can limit mass transfer in chemical reactions. Strategies such as adding co-solvents, structural modifications, and temperature control can improve DES performance [238].

10.1.2.  Improving thermal stability

The use of certain DES in high-temperature industrial processes is limited since they deteriorate at high temperatures. Investigations into DES formulations that are resistant to heat are required [239].

10.1.3.  Fine-tuning polarity and hydrophobicity

The strong hydrophilia of many DESs restricts their use in non-polar settings. The creation of hydrophobic DESs may increase their application in polymer synthesis, extraction, and catalysis. Expand their applicability by modifying the components (for example, utilising hydrophobic hydrogen bond donors); DESs may be customised to dissolve a wide variety of polar or non-polar compounds, increasing their solvent flexibility in extraction, catalysis, and materials synthesis [240].

10.2.   Expanding industrial and commercial applications

Although DES are extensively researched in lab settings, widespread industrial adoption is still in its infancy [241-242]. Future paths consist of:

10.2.1.  DES in carbon capture and climate change mitigation

A viable substitute for amine-based absorption systems, DES has been investigated for CO₂ absorption and sequestration [243]. The development of highly effective CO₂-philic DES has the potential to transform carbon capture technology [244-246].

10.2.2.  DES in energy storage and renewable energy

DES may be used as electrolytes in fuel cells, batteries, and supercapacitors to increase sustainability and energy efficiency [247-248]. To improve ionic conductivity and electrochemical stability for real-world energy applications, more research is required [249].

10.2.3.  DES in food and pharmaceutical industries

Bioactive substances are extracted and purified using DES for use in nutraceuticals and functional meals. creation of drug delivery methods compatible with DES to increase medication solubility and bioavailability [250-255].

10.2.4.  DES for sustainable waste management

DES is being researched for recycling electronic waste, rare earth materials, and polymers.
The circular economy concept may be enhanced by more effective DES-based waste treatment technology [256-257].

10.3.   Regulatory frameworks and safety assessments

The development of standardised regulatory norms is necessary for the widespread adoption of DES in food, pharmaceutical, and environmental applications [258-275]. Future studies ought to look into:

10.3.1.  Toxicity testing and biodegradability studies

Creating thorough toxicity databases for different DES compounds [276-279].

10.3.2.  Eco-toxicological impact

Assessing DES's long-term consequences on the ecosystem in terms of soil, water, and air [280-286].

10.3.3.  Global standardization

Creating global standards for the synthesis, processing, and disposal of DES in order to guarantee sustainability and safety [287-297].

11.    Conclusion

DESs With several applications in extraction, electrochemistry, green chemistry, catalysis, and pharmaceuticals, DESs have emerged as a well-liked, cost-effective, and eco-friendly solvent. Their low toxicity, biodegradability, and tunability make them a potential replacement for conventional solvents and ionic liquids. However, problems including high viscosity, limited industrial scalability, and long-term environmental impact need further research. Future advancements in computational modelling, AI-driven solvent design, and regulatory frameworks will be crucial to overcoming these challenges and realising DES's full potential. DESs has the potential to revolutionise sustainable chemistry and help create a cleaner, greener future with sustained innovation and Interdisciplinary collaboration regarding DESs require to play a role in advancing DES research and practical application. This requires collaboration among chemists, engineers, toxicologists, and industrial partners to optimise formulations, evaluate safety and lifecycle impacts, scale up green processes, and develop application-specific DES systems.

 

ABBREVIATIONS

List of abbreviations

Abbreviation

Full Form

HB

Hydrogen bonding

DESs

Deep eutectic solvents

VOCs

Volatile organic compounds

ΔTf

Freezing point

ILs

Ionic liquids

DNA

Deoxyribonucleic acid

RNA

Ribonucleic acid

HBA

Hydrogen bond acceptor

HBD

Hydrogen bond donor

ChCl

Choline chloride

°C

Degree Celsius

Mp

Melting point

pH

Potential of hydrogen

FTIR

Furious transformation infrared spectroscopy

NMR

Nuclear magnetic resonance

 

AUTHORS CONTRIBUTION

The manuscript was written through the contributions of all authors. All authors have approved the final version of the manuscript.

 

CREDIT AUTHORSHIP CONTRIBUTION STATEMENT

Dr. Benvikram Barman: writing first drafts writing, Is done done by Dr. Manoj Kumar Banjare possesses expertise in various areas including methodology, is reviewed and edited, visualisation, and project administration. Dr. Bhupendra Singh Banjare and Dr. Doly Baghel is done editing, Dr. Amit Kumar Chaturwedi is done review processes, software, verification, Dinesh Tandon is done formal analysis, and Research, tools, data curation. 

 

DATA AVAILABILITY

Data sharing not allowed.

 

NOTES

All authors declare no competing financial interest.

ACKNOWLEDGMENTS

I acknowledge to Dr. Manoj Kumar Banjare Chemistry Division, State Forensic Science Laboratory, Tikrapara, Pujari Park, Raipur, CG, 492001, India he is provide idea for wrting this review.

 

References

1.   Dai Y., spronsen J.V., Witkamp G., Verpoorte R., Choi Y.H., (2013). Natural deep eutectic solvents as new potential media for green technology. Anal. Chim. Acta 766,61-68. https://doi.org/10.1016/j.aca.2012.12.019

2.   X. Zhao, G. Zhu, L. Jiao, F. Yu, C. Xie, Formation and extractive desulfurization mechanisms of aromatic acid based deep eutectic solvents: an experimental and theoretical study, Chem. Eur. J. 24 (2018) 11021–11032, https://doi.org/10.1002/chem.201801631

3.   S.E. Warrag, C. Pototzki, N.R. Rodriguez,M. van Sint Annaland, M.C. Kroon, C. Held, G.Sadowski, C.J. Peters, Oil desulfurization using deep eutectic solvents as sustainable and economical extractants via liquid-liquid extraction: experimental and PC-SAFT predictions, Fluid Phase Equilib. 467 (2018) 33–44, https://doi.org/10.1016/j.fluid. 2018.03.018

4.   Lloret J.O., Vega L.F., Lovell L., (2017), Accurate description of thermophysical properties oAf tetraalkylammonium chloride deep eutectic solvents with the soft-SAFT equation of state. J. fluid., 448,81-93. https://doi.org/10.1016/j.fluid.2017.04.013

5.   Banjare, M. K., Barman, B., Behera, K., Khan, J. M., Banjare, R. K., Pandey, S., & Ghosh, K. K. (2024). Molecular interaction between three novel amino acid based deep eutectic solvents with surface active ionic liquid: A comparative study. Heliyon, 10(15). https://doi.org/10.1016/j.heliyon.2024.e35598

6.   Barman, B., & Banjare, M. K. (2024). Synthesis and characterization of biologically active five amino acids based deep eutectic solvents. Alochana Journal, 13, 1. https://doi.org/20.14118.AJ.2024.V13I1.2161

7.   Kumar, A., Banjare, M. K., Yadav, T., Sinha, S., Sahu, R., Satnami, M. L., Ghosh, K. K., Imidazolium-based ionic liquid as modulator of physicochemical properties of cationic, anionic, nonionic, and gemini surfactants. J. Surfactant Deterg., 21 (2018) 355–366. https://doi.org/10.1002/jsde.12032

8.   Banjare, M. K., Behera, K., Kurrey, R., Banjare, R. K., Satnami, M. L., Pandey, S., Ghosh, K.K., (2018), Self-aggregation of bio-surfactants within ionic liquid 1-ethyl-3- methylimidazolium bromide: a comparative study and potential application in antidepressants drug aggregation. Spectrochim. Acta A Mol. Biomol. Spectrosc., 199 376-386. https://doi.org/10.1016/j.saa.2018.03.079

9.   Barman B., Banjare M.K., (2024), Review of green designer deep eutectic solvents (DESs) production and prospective material science applications., Futuristic trends in chemical material science & nano technology, e-ISBN: 978-93-5747-824-3. IIP series, Volume 3, Book 6, part 2, chapter 8. https://doi.org/10.58532/V3BJCS6P2CH8

10.    Alonso D.A., Baeza A., Chinchilla R., Guillena G., Paster I.M., Ramon D.J., (2016), Deep eutectic solvents: The organic reaction medium of the century. Eur.JOC, 4, 612-632. https://doi.org/10.1002/ejoc.201501197

11.    Z. Li, D. Liu, Z.Men, L. Song, Y. Lv, P.Wu, B. Lou, Y. Zhang, N. Shi, Q. Chen, Insight into effective denitrification and desulfurization of liquid fuel with deep eutectic solvents:an innovative evaluation criterion to filtrate extractants using compatibility index, Green Chem. 20 (2018) 3112–3120, https://doi.org/10.1039/C8GC00828K.

12.    Alonso, D. A., Baeza, A., Chinchilla, R., Guillena, G., Pastor, I. M., & Ramón, D. J. (2016). Deep eutectic solvents: the organic reaction medium of the century. EurJO, 2016(4), 612-632 https://doi.org/10.1002/ejoc.201501197

13.    Zhang, Q., Vigier, K. D. O., Royer, S., & Jérôme, F. (2012). Deep eutectic solvents: syntheses, properties and applications. Chem Soc Rev, 41(21), 7108-7146. https://doi.org/10.1039/C2CS35178A

14.    Sekharan, T. R., Chandira, R. M., Tamilvanan, S., Rajesh, S. C., & Venkateswarlu, B. S. (2022). Deep eutectic solvents as an alternate to other harmful solvents. Biointerface Res. Appl. Chem, 12, 847-860. https://doi.org/10.33263/BRIAC121.847860

15.    E. A. Krisanti, K. Saputra, M.M. Arif, K. Mulia, (2019), Formulation and characterization of betaine-based deep eutectic solvent for extraction phenolic compound from spent coffee grounds, AIP Conf. Proc. 2175, 020040-020048. https://doi.org/10.1063/1.5134604

16.    Llovell Ferret, F. L., Alkhatib, I. I., Ferreira, M. L., Alba, C. G., Bahamon, D., Pereiro, A. B., ... & Vega, L. F. (2020). Screening of ionic liquids and deep eutectic solvents for physical CO2 absorption by soft-SAFT using key performance indicators. J. Chem. Eng. Data. 65, 12, 5844-5861. https://doi.org/10.1021/acs.jced.0c00750

17.    Welton T. (2018), Ionic liquids: a brief history., Biophys.Rev.,10, 691- 706.

18.    Pino V., Afonso AM. (2012), Surface- bonded ionic liquid stationary phases in high- performance liquid chromatography – a review. Analytica Chimica Acta,714:20-37. https://doi.org/10.1016/j.aca.2011.11.045

19.    Werner S, Haumann M, and Wasserscheid P (2010). Ionic liquids in chemical engineering. Annu. Rev. Chem. Biomo. Eng., 1, 203-230. https://doi.org/10.1146/annurev-chembioeng-073009-100915

20.    Shamsuri A.A., Abdullah D.K., (2010), Ionic liquid: preparations and limitations. Makara J. Sci., 14,101-106.

21.    Albert, J., Muller, K. (2014). A group contribution method for the thermal properties of ionic liquids.Ind.Eng.Chem.Res.,53,17522−17526. https://pubs.acs.org/action/showCitFormats?doi=10.1021%2Fie503366p&href=/doi/10.1021%2Fie503366p

22.    Zhang S., Sun N., He x., Lu X., Zhang X., (2006), Physical properties of ionic liquids: Database and Evaluation. J. Phys. Chem. Ref. Data, 35, 1475. https://doi.org/10.1063/1.2204959

23.    Tan Z.Q., Liu J.F., Pang L., (2012), Advances in analytical chemistry using the unique properties of ionic liquids. Trends Anal. Chem., 39,218-227. https://doi.org/10.1016/j.trac.2012.06.005

24.    Greer A.J., Jacquemin J., Hardacre C., (2020). Industrial applications of ionic liquids. Molecules. 25,5207. https://doi.org/10.3390/molecules25215207

25.    Leveque J. M., Cravotto G., (2006), Microwaves, Power Ultrasound, and Ionic Liquids. A New Synergy in Green Organic Synthesis. Chimia, 60, 313-320. https://doi.org/10.2533/000942906777836255

26.    Moon, Y.H., Lee, S.M., Ha, S.H., (2006). Enzyme-catalyzed reactions in ionic liquids. Korean J. Chem. Eng. 23, 247–263. https://doi.org/10.1007/BF02705724

27.    Ahmed A. (2020) Sustainable Organic Synthesis in Ionic Liquids. In: Inamuddin, Asiri A. (eds) Applications of Nanotechnology for Green Synthesis. Nanotechnology in the Life Sciences. Springer, Cham. 978-3-030-44176-0_1. https://doi.org/10.1007/978-3-030-44176-0_1

28.    Lindman, B., Puyal, M. C., Kamenka, N., Rymden, R., Stilbs, P. (1984). Micelle formation of anionic and cationic surfactants from Fourier transform proton and lithium-7 nuclear magnetic resonance and tracer self-diffusion studies. J. Phys. Chem. A, 88, 5048−5057. https://doi.org/10.1021/j150665a051

29.    Jiang L, Deng M, Wang Y, Liang D, Yan Y, and Huang J (2009). Special Effect of β-Cyclodextrin on the Aggregation Behavior of Mixed Cationic/Anionic Surfactant Systems. J. Phys. Chem. B 113, 21, 7498–7504. https://doi.org/10.1021/jp811455f

30.    Fernandez A.S., Leung A.E., Kelley E.G., Jackson A.J., (2021). Complex by design: Hydrotrope – induced micellar growth in deep eutectic solvents. J. Colloid Interface Sci. 581,292-298. https://doi.org/10.1016/j.jcis.2020.07.077\

31.    Sekharan T.R., Chandira R.M., Tamilvanan S., Rajesh S.C., Venkateswarlu B.S., (2022), Deep Eutectic Solvents as an Alternate to other harmful solvents., Biointerface Res. Appl. Chem,12,847-860. https://doi.org/10.33263/BRIAC121.847860

32.    H. Xu, D. Zhang, F. Wu, X. Wei, J. Zhang, Deep desulfurization of fuels with cobalt chloride-choline chloride/polyethylene glycol metal deep eutectic solvents, Fuel 225 (2018) 104–110, https://doi.org/10.1016/j.fuel.2018.03.159.

33.    Santos, F.; Leitao P.S., M.I.; C. Duarte, A.R. (2019), Properties of Therapeutic Deep Eutectic Solvents of l-Arginine and Ethambutol for Tuberculosis Treatment. J. Mol. 24, 24010055.  https://doi.org/10.3390/molecules24010055

34.    Zhang Q., Vigier K.D.O., Royer S.,Jerome F., (2012).deep eutectic solvents: synthesis, properties and applications. Chem. Soc. Rev., 41,7108-7146. https://doi.org/10.1039/C2CS35178A

35.    F. Lima, J. Gouvenaux, L.C. Branco, A.J. Silvestre, I.M. Marrucho, Towards a sulfur clean fuel: deep extraction of thiophene and dibenzothiophene using polyethylene  glycol-based deep eutectic solvents, Fuel 234 (2018) 414–421, https://doi.org/10. 1016/j.fuel.2018.07.043

36.    Florindo C., Oliveira F.S., Rebelo L.P.N., Fernandes A.M., Murrucho I.M., (2014), Insights into the Synthesis and Properties of Deep Eutectic Solvents Based on Cholinium Chloride and Carboxylic Acids, ACS Sustainable Chem.Eng. 10, 2416-2425. https://doi.org/10.1021/sc500439w

37.    Kumar H., Kaur G., (2021). Scrutinizing self-assembly, surface activity and aggregation behavior of mixtures of imidazolium based ionic liquids and surfactants: A comprehensive Review. Front. Chem., 9, 1-23. https://doi.org/10.3389/fchem.2021.667941

38.    Sanchez-Fernandez, A., Arnold, T., Jackson, A. J., Fussell, S. L., Heenan, R. K., Campbell, R. A., Edler, K. J. (2016). Micellization of alkyltrimethylammonium bromide surfactants in choline chloride:glycerol deep eutectic solvent. Phys. Chem. Chem. Phys. 18, 33240−33249. https://doi.org/10.1039/C6CP06053F

39.    Fernandez A. S., Hommond O. S., Jackson A. J., Arnold T., Doutch J., Elder K. J., (2017), Surfactant-Solvent interaction effects on the micellization of cationic surfactants in a carboxylic acid-based deep eutectic solvent, Langmuir,33,14304-14314. https://doi.org/10.1021/acs.langmuir.7b03254

40.    S.E. Warrag, I. Adeyemi, N.R. Rodriguez, I.M. Nashef, M. van Sint Annaland, M.C. roon, C.J. Peters, Effect of the type of ammonium salt on the extractive desulfurization of fuels using deep eutectic solvents, J. Chem. Eng. Data 63 (2018) 1088–1095, https://doi.org/10.1021/acs.jced.7b00832

41.    Alonso, D. A., Baeza, A., Chinchilla, R., Guillena, G., Pastor, I. M., & Ramón, D. J. (2016). Deep eutectic solvents: the organic reaction medium of the century. EurJO, 2016(4), 612-632 https://doi.org/10.1002/ejoc.201501197

42.    Zhang, Q., Vigier, K. D. O., Royer, S., & Jérôme, F. (2012). Deep eutectic solvents: syntheses, properties and applications. Chem Soc Rev, 41(21), 7108-7146. https://doi.org/10.1039/C2CS35178A

43.    Sekharan, T. R., Chandira, R. M., Tamilvanan, S., Rajesh, S. C., & Venkateswarlu, B. S. (2022). Deep eutectic solvents as an alternate to other harmful solvents. Biointerface Res. Appl. Chem, 12, 847-860. https://doi.org/10.33263/BRIAC121.847860

44.    Banjare, M. K., & Barman, B. (2024). Effect of biologically active amino acids based deep eutectic solvents on sodium dodecyl sulfate: A comparative spectroscopic study. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 308, 123700. https://doi.org/10.1016/j.saa.2023.123700

45.    Tang, Z., Wu, C., Tang, W., Ma, C., & He, Y. C. (2023). A novel cetyltrimethylammonium bromide-based deep eutectic solvent pretreatment of rice husk to efficiently enhance its enzymatic hydrolysis. Bioresource Technology, 376, 128806. https://doi.org/10.1016/j.biortech.2023.128806

46.    Banjare, R. K., Banjare, M. K., Behera, K., Pandey, S., & Ghosh, K. K. (2020). Micellization behavior of conventional cationic surfactants within glycerol-based deep eutectic solvent. ACS omega, 5(31), 19350-19362. https://doi.org/10.1021/acsomega.0c00866

47.    Banjare, R. K., Banjare, M. K., Behera, K., Tandon, M., Pandey, S., & Ghosh, K. K. (2021). Deep eutectic solvents as modulator on the micellization behaviour of cationic surfactants and potential application in human serum albumin aggregation. Journal of Molecular Liquids, 344, 117864. https://doi.org/10.1016/j.molliq.2021.117864

48.    Banjare, M. K., Behera, K., Satnami, M. L.; Pandey, S., Ghosh, K. K. (2018). Self-assembly of a short-chain ionic liquid within deep eutectic solvents. RSC Adv. 8, 7969−7979. https://doi.org/10.1039/C7RA13557B

49.    Xu, P., Zheng, GW., Zong, MH. et al. (2017) Recent progress on deep eutectic solvents in biocatalysis. Bioresour. Bioprocess. 4, 34. https://doi.org/10.1186/s40643-017-0165-5

50.    Bajkacz S., Adamek J., Sobska A., (2020). Application of deep eutectic solvents and ionic liquids in the extraction of catechins from tea. Molecules,25,3216. https://doi.org/10.3390/molecules25143216

51.    Liu, Y., Friesen, J. B., McAlpine, J. B., Lankin, D. C., Chen, S. N., Pauli, G. F. (2018). Natural deep eutectic solvents: properties, applications, and perspectives. J. Nat. Prod. 3, 679−690. https://doi.org/10.1021/acs.jnatprod.7b00945 

52.    Pinho, M. R., Lima, A. S., de Almeida Ribeiro Oliveira, G., Liao, L. M., Franceschi, E., Silva, R. D., & Cardozo-Filho, L. (2024). Choline chloride-and organic acids-based deep eutectic solvents: Exploring chemical and thermophysical properties. Journal of Chemical & Engineering Data69(10), 3403-3414. https://doi.org/10.1021/acs.jced.3c00706

53.    Duan L., Dou L.L., Guo L.,Li P.Liu E., (2016). Comprehensive evalution of deep eutectic solvents in extraction of bioactive natural products. ACS Sustainable Chem.Eng., 4, 2405-2411. https://doi.org/10.1021/acssuschemeng.6b00091

54.    Fernandez A.S., Hammond O.S., Jackson A.J., Arnold T., Doutch J., Edler K.J., (2017), Surfactant- solvent interaction effects on the micellization of cationic surfactants in a carboxylic acid- based deep eutectic solvent, Langmur,33,14304-14314. https://doi.org/10.1021/acs.langmuir.7b03254

55.    González-Campos, J. B., Pérez-Nava, A., Valle-Sánchez, M., & Delgado-Rangel, L. H. (2024). Deep eutectic solvents applications aligned to 2030 United Nations Agenda for Sustainable Development. Chemical Engineering and Processing-Process Intensification199, 109751.  https://doi.org/10.1016/j.cep.2024.109751

56.    Długosz, O., & Banach, M. (2024). Green methods for obtaining deep eutectic solvents (DES). Journal of Cleaner Production434, 139914. https://doi.org/10.1016/j.jclepro.2023.139914

57.    Długosz O. (2023), Natural Deep Eutectic Solvents in the Synthesis of Inorganic Nanoparticles. Materials. 16(2):627. https://doi.org/10.3390/ma16020627

58.    Arnodo, D., Maffeis, E., Marra, F., Nejrotti, S., & Prandi, C. (2023). Combination of enzymes and deep eutectic solvents as powerful toolbox for organic synthesis. Molecules, 28(2),516. https://doi.org/10.3390/molecules28020516

59.    Smith, E. L., Abbott, A. P., & Ryder, K. S. (2014). Deep eutectic solvents (DESs) and their         applications. Chemical reviews, 114(21), 11060-11082.  https://doi.org/10.1021/cr300162p

60.    Canadas, R.; González-Miquel, M.; González, E.J. Overview of neoteric solvents as extractants in food industry: A focus on phenolic compounds separation from liquid streams. Food Res. Int. 2020, 136, 109558. https://doi.org/10.1016/j.foodres.2020.109558 

61.    Gonzalez, E.J.; Díaz, I.; Gonzalez-Miquel, M. On the behavior of imidazolium versus pyrrolidinium ionic liquids as extractants of phenolic compounds from water: Experimental and computational analysis. Sep. Purif. Technol. 2018, 201, 214–222. https://doi.org/10.1016/j.seppur.2018.03.006

62.    Ni, H.; Dong, J.; Shi, J. Ionic liquid as extraction agent for detection of volatile phenols in wastewater and its regeneration. J. Sep. Sci. 2015, 33, 1356–1359. https://doi.org/10.1002/jssc.200900730

63.    Sas, O.G.; Domínguez, I.; González, B. Liquid-liquid extraction of phenolic compounds from water using ionic liquids: Literature review and new experimental data using [C2mim]FSI. J. Environ. Manag. 2018, 228, 475–482. https://doi.org/10.1016/j.jenvman.2018.09.042

64.    Chen, Y.; Liang, H.; Qin, X. Cheap and biodegradable amino acid-based deep eutectic solvents for radioactive iodine capture via halogen bonds. J. Mol. Liq. 2020, 303, 112615. https://doi.org/10.1016/j.molliq.2020.112615

65.    Maneffa, A.J.; Harrison, A.B.; Radford, S.J. Deep eutectic solvents based on natural ascorbic acid analogues and choline chloride. ChemistryOpen 2020, 9, 559–567. https://doi.org/10.1002/open.202000020

66.    Durand, E., Lecomte, J., & Villeneuve, P. (2013). Deep eutectic solvents: Synthesis, application, and focus on lipase‐catalyzed reactions. Eur J Lipid Sci Technol, 115(4), 379-385. https://doi.org/10.1002/ejlt.201200416

67.    Qin, H., Hu, X., Wang, J., Cheng, H., Chen, L., & Qi, Z. (2020). Overview of acidic deep eutectic solvents on synthesis, properties and applications. GEE, 5(1), 8-21. https://doi.org/10.1016/j.gee.2019.03.002

68.    Banjare, M. K., Behera, K., Satnami, M. L., Pandey, S., & Ghosh, K. K. (2018). Self-assembly of a short-chain ionic liquid within deep eutectic solvents. RSC advances, 8(15), 7969-7979. https://doi.org/10.1039/C7RA13557B

69.    Lakshmi, A.B.; Balasubramanian, A.; Venkatesan, S. Extraction of phenol and chlorophenols using ionic liquid [Bmim]+[BF4], dissolved in tributyl phosphate. CLEAN Soil Air Water. 2013, 41, 349–355. https://doi.org/10.1002/clen.201100632

70.    Dai, Y.; van Spronsen, J.; Witkamp, G.J. Natural deep eutectic solvents as new potential media for green technology. Anal. Chim. Acta 2013, 766, 61–68. https://doi.org/10.1016/j.aca.2012.12.019

71.    Abbott, A.P.; Capper, G.; Davies, D.L. Novel solvent properties of choline chloride/urea mixtures. Chem. Commun. 2003, 9, 70–71. https://doi.org/10.1039/B210714G

72.    Al-Risheq D.I.M., Shaikh S.M.R., Nasser M.S., Almomani F., Hussein I.A., Hassan M.K., Enhancing the flocculation of stable bentonite suspension using hybrid system of polyelectrolytes and NADES J. Col. Surface A Physicochem.And Eng. Aspects, 638,2022,128305. https://doi.org/10.1016/j.colsurfa.2022.128305

73.    P.Abbot A., Ttaib K.E., Frisch G., Electrodeposition of copper composites from deep eutectic solvents based on choline chloride, J. physical chemistry chemical physics., 11,2009, 4269-4277. https://doi.org/10.1039/B817881J

74.    Kudlak B., Owczarek K., Namiesnik J., Selected issues related to the toxicity of ionic liquids and deep eutectic solvents—a review. J. Environment Sci. Pollution Res., 22,2015,11975-11992. https://doi.org/10.1007/s11356-015-4794-y

75.    Nahar y., Thickett S.C., Greener, Faster, Stronger: The Benefits of Deep Eutectic Solvents in Polymer and Materials Science, Polymers, 13(3) 2021, 447. https://doi.org/10.3390/polym13030447

76.    Taghizadeh M., taghizadeh A., Vatanpour V., Ganjali M.R., Saeb M.R., Deep eutectic solvents in membrane science and technology: Fundamental, preparation, application, and future perspective., J. Sep.Pur.Tech., 258,2021,118015. https://doi.org/10.1016/j.seppur.2020.118015

77.    Li X., Row K.H., Application of novel ternary deep eutectic solvents as a functional monomer in molecularly imprinted polymers for purification of levofloxacin, J. chromatography B., 1068-1069,2017,56-63. https://doi.org/10.1016/j.jchromb.2017.10.012

78.    Ruesgas- Ramon M., Figueroa- Espinoza M.C., and Durand E., Application of Deep Eutectic Solvents (DES) for Phenolic Compounds Extraction: Overview, Challenges, and Opportunities, J. Agric. Food chem., 65,18,2017,3591-3601. https://doi.org/10.1021/acs.jafc.7b01054

79.    Abo-Hamad A., Hayyan M., Alsaadi M.A.H., Hashim M.A., Potential applications of deep eutectic solvents in nanotechnology, J.Chem. Eng. J., 273,2015,551-567. https://doi.org/10.1016/j.cej.2015.03.091

80.    Tang B., Zhang H., Row K.H., Application of deep eutectic solvents in the extraction and separation of target compounds from various samples J. Sep. Sci.,38,2015,1053-1064. https://doi.org/10.1002/jssc.201401347

81.    Vigier K.D.O., Chatel G., Jerome F., (2015). Contribution of deep eutectic solvents for biomass processing: opportunities, challenges, and limitations. Chemcatchem, 7,1250-1260. https://doi.org/10.1002/cctc.201500134

82.    Garcia G., Aparicio S., Ullah R., Atilhan M., (2015). Deep eutectic solvents: physicochemical properties and gas separation applications. Energy & fuels,29,2616-2644. https://doi.org/10.1021/ef5028873

83.    Li X.,Row K.H.,(2016).Development of deep eutectic solvents applied in extraction and separation. J. Sep. Sci, 39, 3505-3520. https://doi.org/10.1002/jssc.201600633

84.    Sarmad S., Mikkola J.P., Ji X., (2016). Carbon dioxide capture with ionic liquids and deep eutectic solvents: A new generation of sorbents A review. Chemsuschem, 10, 324-352. https://doi.org/10.1002/cssc.201600987

85.    Liu, P.; Hao, J. W.; Mo, L. P.; Zhang, Z. H. (2015). Recent advances in the application of deep eutectic solvents as sustainable media as well as catalysts in organic reactions. RSC Adv. 5, 48675−48704. https://doi.org/10.1039/C5RA05746A

86.    Zdziennicka A., Szymczyk K., Krawczyk J., Janczuk., (2012). Critical micelle concentration of some surfactants and thermodynamic parameters of their micellization. Fluid Phase. Equilibria. 322-323,126-134. https://doi.org/10.1016/j.fluid.2012.03.018

87.    Shi Y., Luo H.Q., Li N.B., (2011), Determination of the critical premicelle concentration, first critical micelle concentration and second critical micelle concentration of surfactants by resonance Rayleigh scattering method without any probe. Spectrochim. Acta A Mol. Biomol. Spectrosc., 78,1403-1407. https://doi.org/10.1016/j.saa.2011.01.018

88.    El Achkar, T., Greige-Gerges, H., & Fourmentin, S. (2021). Basics and properties of deep eutectic solvents: a review. Environmental chemistry letters, 19, 3397-3408. https://doi.org/10.1007/s10311-021-01225-8

89.    Zhang, M., Zhang, X., Liu, Y., Wu, K., Zhu, Y., Lu, H., & Liang, B. (2021). Insights into the relationships between physicochemical properties, solvent performance, and applications of deep eutectic solvents. Environmental Science and Pollution Research, 28(27), 35537-35563. https://doi.org/10.1007/s11356-021-14485-2

90.    Li, Q., Jiang, J., Li, G., Zhao, W., Zhao, X., & Mu, T. (2016). The electrochemical stability of ionic liquids and deep eutectic solvents. Science China Chemistry, 59, 571-577. https://doi.org/10.1007/s11426-016-5566-3

91.    Jiang H.J., Atkin R., G. Warr G., Nanostructured ionic liquids and their solutions: Recent advances and emerging challenges, Curr. Opin. Green Sustain. Chem., 12, 2018, 27-32. https://doi.org/10.1016/j.cogsc.2018.05.003

92.    Rahman M. S., Roy R., Montoya, C., Halim M.A., Raynie D. E., Acidic and basic amino acid-based novel deep eutectic solvents and their role in depolymerization of lignin, J. Mol. Liq., 362, 2022, 119751. https://doi.org/10.1016/j.molliq.2022.119751

93.    Li, M., Liu, Y., Hu, F., Ren H., and Duan, E., Amino acid-based natural deep eutectic solvents for extraction of phenolic compounds from aqueous Environments, Processes 2021, 9(10), 1716. https://doi.org/10.3390/pr9101716

94.    A. Zdziennicka, K. Szymczyk, J. Krawczyk, Janczuk, Critical micelle concentration of some surfactants and thermodynamic parameters of their micellization, Fluid Phase Equilibria 322–323 (2012) 126–134. https://doi.org/10.1016/j.fluid.2012.03.018

95.    Y. Shi, H.Q. Luo, N.B. Li, Determination of the critical premicelle concentration, first critical micelle concentration and second critical micelle concentration of surfactants by resonance Rayleigh scattering method without any probe, Spectrochim. Acta A Mol. Biomol. Spectrosc. 78 (2011) 1403–1407. https://doi.org/10.1016/j.saa.2011.01.018

96.    F. M. Manger, J.U. Rhee, H.K. Rhee, Applications of surfactants to synthetic organic chemistry, J. Org. Chem. 40 (1975) 3803–3805. https://doi.org/10.1021/jo00913a051

97.    Abbott, A. P., Capper, G., Davies, D. L., Rasheed, R. K., & Tambyrajah, V. (2003). Novel solvent properties of choline chloride/urea mixtures. Chemical communications, (1), 70-71. https://doi.org/10.1039/B210714G

98.    A. P. Abbott, et al. "Deep eutectic solvents formed between choline chloride and carboxylic acids: versatile alternatives to ionic liquids." Journal of the American Chemical Society, Vol. 126, No. 29, pp. 9142-9147, 2004. https://doi.org/10.1021/ja048266j

99.    M. A. Kareem, F.S. Mjalli, M.A. Hashim, I. M. J. AlNashed "Phosphonium-based ionic liquids analogues and their physical properties" Chem. Eng. Data, Vol. 55, No. 11, pp. 4632-4637, 2010. https://doi.org/10.1021/je100104v

100.     A. P. Abbott, et al. "Eutectic‐based ionic liquids with metal‐containing anions and cations" Chemistry–A European Journal, Vol.13, No. 22, pp. 6495-6501, 2007. https://doi.org/10.1002/chem.200601738

101.     Affat, S. (2024). A review of deep eutectic solvents (DESs), Preparation, Classification, Physicochemical properties, Advantages and disadvantages. University of Thi-Qar Journal of Science, 11(1), 166-174. https://doi.org/10.32792/utq/utjsci/v11i1.1208

102.     A. Bhardwaj, S. Hartland, Applications of surfactants in petroleum industry, J. Dispers. Sci. Technol. 14 (1993) 87–116. https://doi.org/10.1080/01932699308943389

103.     M. Abe, Synthesis and applications of surfactants containing fluorine, Curr. Opin. Colloid Interface Sci. 4 (1999) 354–356. https://doi.org/10.1016/S1359-0294(99)90017-1

104.     M. Summers, J. Eastoe, Applications of polymerizable surfactants, Adv. Colloid Interface Sci. 100–102 (2003) 137–152. https://doi.org/10.1016/S0001-8686(02)00058-1

105.     B. Lindman, M.C. Puyal, N. Kamenka, R. Rymden, P. Stilbs, Micelle formation of anionic and cationic surfactants from Fourier transform proton and lithium-7 nuclear magnetic resonance and tracer self-diffusion studies, J. Phys. Chem. A 88 (1984) 5048–5057. https://doi.org/10.1021/j150665a051

106.     A. Sanchez-Fernandez, T. Arnold, A.J. Jackson, S.L. Fussell, R.K. Heenan, R. A. Campbell, K.J. Edler, Micellization of alkyltrimethylammonium bromide surfactants in choline chloride:glycerol deep eutectic solvent, Phys. Chem. Chem. Phys. 18 (2016) 33240–33249. https://doi.org/10.1039/C6CP06053F

107.     K.H. Almashjary, M. Khalid, S. Dharaskar, P. Jagadish, R. Walvekar, T.C.S.M. Gupta, Optimisation of extractive desulfurization using Choline Chloride-based deep eutectic solvents, Fuel 234 (2018) 1388–1400, https://doi.org/10.1016/j.fuel.2018.08.005.

108.     García, G., Aparicio, S., Ullah, R., & Atilhan, M. (2015). Deep eutectic solvents: physicochemical properties and gas separation applications. Energy & Fuels, 29(4), 2616-2644. https://doi.org/10.1021/ef5028873

109.     D. J. G. P Van Osch, C. H. J. T. Dietz, S. E. E. Warrag, M. C. Kroon "The curious case of hydrophobic deep eutectic solvents: a story on the discovery, design, and applications" ACS Sustain. Chem. Eng., Vol. 8, 2020. https://doi.org/10.1021/acssuschemeng.0c00559

110.     Y. Dai, J. Van Spronsen, G. J. Witkamp, R. Verpoorte, Y. H. Choi "Natural deep eutectic solvents as new potential media for green technology" Anal. Chim. Acta , Vol. 766, pp. 61-68, 2013. https://doi.org/10.1016/j.aca.2012.12.019

111.     R. K. Ibrahim, M. Hayyan, M. A. AlSaadi, S. Ibrahim, A. Hayyan, M. A. Hashim "Physical properties of ethylene glycol-based deep eutectic solvents, J. Mol. Liq. pp. 276 794-800, 2019. https://doi.org/10.1016/j.molliq.2018.12.032

112.     M. A. R. Martins, E. A. Crespo, P. V. A. Pontes, L. P. Silva, M. Bülow, G. J. Maximo, E. A. C. Batista, C. Held, S. P. Pinho, J. A. P Coutinho "Tunable hydrophobic eutectic solvents based on terpenes and monocarboxylic acids" ACS Sustain. Chem. Eng, Vol. 6, pp. 8836-8846, 2018. https://doi.org/10.1021/acssuschemeng.8b01203

113.     W. Guo, Y. Hou, S. Ren, S. Tian, W. Wu "Formation of deep eutectic solvents by phenols and choline chloride and their physical properties, J. Chem. Eng. Data, Vol. 58, pp. 866-872, 2013. https://doi.org/10.1021/je300997v

114.     W. Lu, S. Liu, Z. Wu "Recent application of deep eutectic solvents as green solvent in dispersive liquid-liquid microextraction of trace level 173 chemical contaminants in food and water" Crit. Rev. Anal. Chem. , Vol. 52, pp. 504-518, 2022. https://doi.org/10.1080/10408347.2020.1808947

115.     L. Nakhle, M. Kfoury, I. Mallard, D. Landy, H. Greige-Gerges "Microextraction of bioactive compounds using deep eutectic solvents: a review" Environ. Chem. Lett., Vol. 19, pp. 3747-3759, 2021. https://doi.org/10.1007/s10311-021-01255-2

116.     Y. Chen, W. Chen, L. Fu, Y. Yang, Y. Wang, X. Hu, F. Mu. T. Wang "Surface tension of 50 deep eutectic solvents: effect of hydrogen-bonding donors, hydrogen-bonding acceptors, other solvents, and temperature" Ind. Eng. Chem. Res., Vol. 58, pp. 12741-12750, 2019. https://doi.org/10.1021/acs.iecr.9b00867

117.     Fukuzumi, S., Lee, Y. M., & Nam, W. (2019). Structure and reactivity of the first-row d-block metal-superoxo complexes. Dalton Transactions48(26), 9469-9489. https://doi.org/10.1039/C9DT01402K

118.     D.E. Crawford, L.A. Wright, S.L. James, A.P. Abbott., Chem. Commun. 52, (2016), 4215-4218. https://doi.org/10.1039/C5CC09685E

119.     Manikandan, V., & Lee, N. Y. (2022). Green synthesis of carbon quantum dots and their environmental applications. Environmental Research212, 113283. https://doi.org/10.1016/j.envres.2022.113283

120.     B. Tang, W. Bi, H. Zhang, K. H. Row "Deep eutectic solvent-based HS-SME coupled with GC for the analysis of bioactive terpenoids in Chamaecyparis obtuse leaves" Chromatographia, Vo.l. 77, 373-377, 2014. https://doi.org/10.1007/s10337-013-2607-3

121.     L. Nakhle, M. Kfoury, I. Mallard, D. Landy, H. Greige-Gerges "Microextraction of bioactive compounds using deep eutectic solvents: a review" Environ. Chem. Lett., Vol. 19, pp. 3747-3759, 2021. https://doi.org/10.1007/s10311-021-01255-2

122.     Ren, S., Mu, T., & Wu, W. (2023). Advances in deep eutectic solvents: New green solvents. Processes11(7), 1920. https://doi.org/10.3390/pr11071920

123.     Sitze, S. Melissa, et al. "Ionic liquids based on FeCl3 and FeCl2. Raman scattering and ab initio calculations" Inorganic chemistry, Vol. 40, No. 10, pp. 2298-2304, 2001. https://doi.org/10.1021/ic001042r

124.     Eliel, E. L., & Mosher, H. S. (1975). The 1975 Nobel Prize for Chemistry. Science190(4216), 772-774. https://doi.org/10.1126/science.190.4216.772

125.     T. B Scheffler, M. S. Thomson, In Seventh International Conference on Molten Salts; The Electrochemical Society: Montreal, p 281, 1990. https://doi.org/10.1016/0013-4686(96)00080-1

126.     El Abedin, S. Zein, et al. "Electrodeposition of selenium, indium and copper in an air-and water-stable ionic liquid at variable temperatures." Electrochimica Acta, Vol. 52, No. 8, pp. 2746-2754, 2007. https://doi.org/10.1016/j.electacta.2006.08.064

127.     S. A. Bolkan, , and T. J. Yoke. "Room temperature fused salts based on copper (I) chloride-1-methyl-3-ethylimidazolium chloride mixtures. 1. Physical properties" Journal of Chemical and Engineering Data, pp. 194-197, 1986. https://doi.org/10.1021/je00044a019

128.     Yang, Jia-Zhen, et al. "Studies on mixture of ionic liquid EMIGaCl4 and EMIC." Fluid Phase Equilibria, Vol. 227, No. 1, pp. 41- 46, 2005. https://doi.org/10.1016/j.fluid.2004.10.026

129.     L. Emma, Smith, A.P. Abbott and S. Karl, S. Ryder "Deep eutectic solvents (DESs) and their applications, Chemical. Reviews, Vol.114, pp.11060−11082, 2014. https://doi.org/10.1021/cr300162p

130.     Piemontese, L., Sergio, R., Rinaldo, F., Brunetti, L., Perna, F. M., Santos, M. A., & Capriati, V. (2020). Deep eutectic solvents as effective reaction media for the synthesis of 2-hydroxyphenylbenzimidazole-based scaffolds en route to donepezil-like compounds. Molecules, 25(3), 574. https://doi.org/10.3390/molecules25030574

131.     Leron, R. B., Soriano, A. N., & Li, M. H. (2012). Densities and refractive indices of the deep eutectic solvents (choline chloride+ ethylene glycol or glycerol) and their aqueous mixtures at the temperature ranging from 298.15 to 333.15 K. Journal of the Taiwan Institute of Chemical Engineers, 43(4), 551-557. https://doi.org/10.1016/j.jtice.2012.01.007

132.     Li, C. J., & Anastas, P. T. (2012). Green Chemistry: present and future. Chemical Society Reviews41(4), 1413-1414. https://doi.org/10.1039/C1CS90064A

133.     M.K.H. Kali, K.E.A. Khidir, I. Wazeer, L.E. Blidi, S. Mulyono, I.M. AlNashef, Application of deep eutectic solvents and their individual constituents as surfactants for enhanced oil recovery, Col. Surfa. A 487 (2015) 221–231. https://doi.org/10.1016/j.colsurfa.2015.10.005

134.     M. Pal, R. Rai, A. Yadav, R. Khanna, G.A. Baker, S. Pandey, Self-Aggregation of Sodium Dodecyl Sulfate within (Choline Chloride + Urea) Deep Eutectic Solvent, Langmuir 30 (44) (2014) 13191–13198. https://doi.org/10.1021/la5035678

135.     T. Arnold, A.J. Jackson, A. Sanchez-Fernandez, D. Magnone, A.E. Terry, K.J. Edler, Surfactant Behavior of Sodium Dodecylsulfate in Deep Eutectic Solvent Choline Chloride/ Urea, Langmuir 31 (47) (2015) 12894–12902. https://doi.org/10.1021/acs.langmuir.5b02596

136.     Tucker, J. L. (2006). Green chemistry, a pharmaceutical perspective. Organic process research & development10(2), 315-319. https://doi.org/10.1021/op050227k

137.     Vigier, K. D. O., Chatel, G., & Jérôme, F. (2015). Contribution of deep eutectic solvents for biomass processing: opportunities, challenges, and limitations. ChemCatChem, 7(8), 1250-1260. https://doi.org/10.1002/cctc.201500134

138.     Sekharan, T. R., Chandira, R. M., Tamilvanan, S., Rajesh, S. C., & Venkateswarlu, B. S. (2022). Deep eutectic solvents as an alternate to other harmful solvents. Biointerface Res. Appl. Chem, 12(1), 847-860. https://doi.org/10.33263/BRIAC121.847860

139.     Płotka-Wasylka, J., De la Guardia, M., Andruch, V., & Vilková, M. (2020). Deep eutectic solvents vs ionic liquids: Similarities and differences. Microchemical Journal, 159, 105539. https://doi.org/10.1016/j.microc.2020.105539

140.     Canales, R. I., & Brennecke, J. F. (2016). Comparison of ionic liquids to conventional organic solvents for extraction of aromatics from aliphatics. Journal of Chemical & Engineering Data, 61(5), 1685-1699. https://doi.org/10.1021/acs.jced.6b00077

141.     Vanda, H., Dai, Y., Wilson, E. G., Verpoorte, R., & Choi, Y. H. (2018). Green solvents from ionic liquids and deep eutectic solvents to natural deep eutectic solvents. Comptes Rendus Chimie, 21(6), 628-638. https://doi.org/10.1016/j.crci.2018.04.002

142.     M.K. Banjare, R. Kurrey, T. Yadav, S. Sinha, M.L. Satnami, K.K. Ghosh, A comparative study on the effect of imidazolium-based ionic liquid on self-aggregation of cationic, anionic and nonionic surfactants studied by surface tension, conductivity, fluorescence and FTIR spectroscopy, J. Mol. Liq. 241 (2017) 622–632. https://doi.org/10.1016/j.molliq.2017.06.009

143.     Lima, F., Branco, L. C., Silvestre, A. J., & Marrucho, I. M. (2021). Deep desulfurization of fuels: Are deep eutectic solvents the alternative for ionic liquids?. Fuel, 293, 120297. https://doi.org/10.1016/j.fuel.2021.120297

144.     A. Kumar, M.K. Banjare, T. Yadav, S. Sinha, R. Sahu, M.L. Satnami, K.K. Ghosh, Imidazolium-based ionic liquid as modulator of physicochemical properties of cationic, anionic, nonionic, and gemini surfactants, J. Surfactant Deterg. 21 (2018) 355–366. https://doi.org/10.1002/jsde.12032

145.     R.K. Banjare, M.K. Banjare, S. Panda, Effect of acetonitrile on the colloidal behavior of conventional cationic surfactants: a combined conductivity, surface tension, fluorescence and FTIR study, J. Solution Chem. 49 (2020) 34–51. https://doi.org/10.1007/s10953-019-00937-4

146.     M.K. Banjare, K. Behera, R. Kurrey, R.K. Banjare, M.L. Satnami, S. Pandey, K. K. Ghosh, Self-aggregation of bio-surfactants within ionic liquid 1-ethyl-3- methylimidazolium bromide: a comparative study and potential application in antidepressants drug aggregation, Spectrochim. Acta A 199 (2018) 376–386. https://doi.org/10.1016/j.saa.2018.03.079

147.     Kalidindi, S. B., & Jagirdar, B. R. (2012). Nanocatalysis and prospects of green chemistry. ChemSusChem5(1), 65-75. https://doi.org/10.1002/cssc.201100377

148.     M.A. Rub, N. Azum, D. Kumar, A.M. Asiri, Interaction of TX-100 and antidepressant imipramine hydrochloride drug mixture: surface tension, 1H-NMR, and FTIR, Gels 8 (2022) 159. https://doi.org/10.3390/gels8030159

149.     A. Goel, S. Tomar, S. Tomar, A facile synthesis and characterization of surfactant (CTAB/TSC/TX-100) assisted Ir-Sn bimetallic nanoparticles, J. Nanostruct. 10 (2020) 846–862. https://doi.org/10.22052/JNS.2020.04.018

150.     Prabhune, A., & Dey, R. (2023). Green and sustainable solvents of the future: Deep eutectic solvents. Journal of Molecular Liquids379, 121676. https://doi.org/10.1016/j.molliq.2023.121676

151.     Afonso, J., Mezzetta, A., Marrucho, I. M., & Guazzelli, L. (2023). History repeats itself again: Will the mistakes of the past for ILs be repeated for DESs? From being considered ionic liquids to becoming their alternative: The unbalanced turn of deep eutectic solvents. Green Chemistry25(1), 59-105. https://doi.org/10.1039/D2GC03198A

152.     A. Shishov, A. Bulatov, M. Locatelli, S. Carradori, V. Andruch, Application of deep eutectic solvents in analytical chemistry, A review. Microchem. J. 135 (2017) 33–38. https://doi.org/10.1016/j.microc.2017.07.015

153.     Merza, F., Fawzy, A., AlNashef, I., Al-Zuhair, S., & Taher, H. (2018). Effectiveness of using deep eutectic solvents as an alternative to conventional solvents in enzymatic biodiesel production from waste oils. Energy Reports, 4, 77-83. https://doi.org/10.1016/j.egyr.2018.01.005

154.     M.S. Kamal, I.A. Hussein, A.S. Sultan, Review on surfactant flooding: phase behavior, retention, IFT, and field applications, Energy Fuels 31 (2017) 7701–7720. https://doi.org/10.1021/acs.energyfuels.7b00353

155.     Sheldon, R. A. (2012). Fundamentals of green chemistry: efficiency in reaction design. Chemical Society Reviews41(4), 1437-1451. https://doi.org/10.1039/C1CS15219J

156.     Hjeresen, D. L., Boese, J. M., & Schutt, D. L. (2000). Green chemistry and education. Journal of Chemical Education77(12), 1543. https://doi.org/10.1021/ed077p1543

157.     M. Pal, R.K. Singh, S. Pandey, Evidence of self-aggregation of cationic surfactants in a choline chloride+ glycerol deep eutectic solvent, Chem. Phys. Chem. 16 (2015) 2538–2542. https://doi.org/10.1002/cphc.201500357

158.     Zhang, Y.; Li, Z.;Wang, H. Efficient separation of phenolic compounds from model oil by the formation of choline derivative-based deep eutectic solvents. Sep. Purif. Technol. 2016, 163, 310–318. https://doi.org/10.1016/j.seppur.2016.03.014

159.     Martinez, R.; Berbegal, L.; Guillena, G. Bio-renewable enantioselective aldol reaction in natural deep eutectic solvents. Green Chem. 2016, 47, 1724–1730. https://doi.org/10.1039/C5GC02526E

160.     Shishov, A.; Pochivalov, A.; Nugbienyo, L. Deep eutectic solvents are not only effective extractants. TrAC Trends Anal. Chem. 2020, 219, 115956. https://doi.org/10.1016/j.trac.2020.115956

161.     Herrmann, J. M., Duchamp, C., Karkmaz, M., Hoai, B. T., Lachheb, H., Puzenat, E., & Guillard, C. (2007). Environmental green chemistry as defined by photocatalysis. Journal of hazardous materials146(3), 624-629. https://doi.org/10.1016/j.jhazmat.2007.04.095

162.     Mako, P.; Supek, E.; Gbicki, J. Hydrophobic deep eutectic solvents in microextraction techniques—A review. Microchem. J. 2019, 152, 104384. https://doi.org/10.1016/j.microc.2019.104384

163.     Mei, X.; Li, J.; Jing, C.; Fang, C. Separation and recovery of phenols from an aqueous solution by a green membrane system. J. Clean. Prod. 2019, 251, 119675. https://doi.org/10.1016/j.jclepro.2019.119675

164.     Zhang, M.; Zhang, Z.; Liu, S. Ultrasound-assisted electrochemical treatment for phenolic wastewater. Ultrason. Sonochem. 2020, 65, 105058. https://doi.org/10.1016/j.ultsonch.2020.105058

165.     Florindo, C.; Monteiro, N.V.; Ribeiro, B.D. Hydrophobic deep eutectic solvents for purification of water contaminated with bisphenol-a. J. Mol. Liq. 2020, 297, 111841. https://doi.org/10.1016/j.molliq.2019.111841

166.     Florindo, C.; Branco, L.C.; Marrucho, I.M. Development of hydrophobic deep eutectic solvents for extraction of pesticides from aqueous environments. Fluid Phase Equilib. 2017, 448, 135–142. https://doi.org/10.1016/j.fluid.2017.04.002

167.     De Marco, B. A., Rechelo, B. S., Tótoli, E. G., Kogawa, A. C., & Salgado, H. R. N. (2019). Evolution of green chemistry and its multidimensional impacts: A review. Saudi pharmaceutical journal27(1), 1-8. https://doi.org/10.1016/j.jsps.2018.07.011

168.     Clark, J. H. (2002). Solid acids for green chemistry. Accounts of chemical research35(9), 791-797. https://doi.org/10.1021/ar010072a

169.     Zhekenov, T.; Toksanbayev, N.; Kazakbayeva, Z. Formation of type III deep eutectic solvents and effect of water on their intermolecular interactions. Fluid Phase Equilib. 2017, 441, 43–48.

170.     Ma, C.; Guo, Y.; Li, D. Molar enthalpy of mixing and refractive indices of choline chloride-based deep eutectic solvents with water. Chem. Thermodyn. 2017, 105, 30–36.

171.     Dai, Y.;Witkamp, G.J.; Verpoorte, R. Tailoring properties of natural deep eutectic solvents with water to facilitate their applications. Food Chem. 2015, 187, 14–19.

172.     Ji, Y.; Hou, Y.; Ren, S. Separation of phenolic compounds from oil mixtures using environmentally benign biological reagents based on Brønsted acid-Lewis base interaction. Fuel 2019, 239, 926–934.

173.     Zhang, Y.; Chang, C.; Tan, B. Application of a Sustainable Bioderived Solvent (Biodiesel) for Phenol Extraction. ACS Omega 2019, 4, 10431–10437.

174.     Galbe, M., & Wallberg, O. (2019). Pretreatment for biorefineries: a review of common methods for efficient utilisation of lignocellulosic materials. Biotechnology for biofuels, 12(1), 294.

175.     Liu, Y., Chen, W., Xia, Q., Guo, B., Wang, Q., Liu, S., ... & Yu, H. (2017). Efficient cleavage of lignin–carbohydrate complexes and ultrafast extraction of lignin oligomers from wood biomass by microwave‐assisted treatment with deep eutectic solvent. ChemSusChem, 10(8), 1692-1700.

176.     Alvarez-Vasco, C., Ma, R., Quintero, M., Guo, M., Geleynse, S., Ramasamy, K. K., ... & Zhang, X. (2016). Unique low-molecular-weight lignin with high purity extracted from wood by deep eutectic solvents (DES): a source of lignin for valorization. Green chemistry, 18(19), 5133-5141.

177.     Płotka-Wasylka, J., De la Guardia, M., Andruch, V., & Vilková, M. (2020). Deep eutectic solvents vs ionic liquids: Similarities and differences. Microchemical Journal, 159, 105539.

178.     Kang, S., Fu, J., & Zhang, G. (2018). From lignocellulosic biomass to levulinic acid: A review on acid-catalyzed hydrolysis. Renewable and Sustainable Energy Reviews, 94, 340-362.

179.     Zhou, L., Zhang, M., Huo, Y., Bai, L., He, S., Wang, J., ... & Guo, X. (2022). Green Energy Environ. 2022. press. https://doi.org/10.1016/j.gee,3 

180.     Rasmussen, H., Sørensen, H. R., & Meyer, A. S. (2014). Formation of degradation compounds from lignocellulosic biomass in the biorefinery: sugar reaction mechanisms. Carbohydrate research, 385, 45-57.

181.     Feng, Y., Li, M., Gao, Z., Zhang, X., Zeng, X., Sun, Y., ... & Lin, L. (2019). Development of betaine‐based sustainable catalysts for green conversion of carbohydrates and biomass into 5‐hydroxymethylfurfural. ChemSusChem, 12(2), 495-502.

182.     Gomes, G. R., & Pastre, J. C. (2020). Microwave-assisted HMF production from water-soluble sugars using betaine-based natural deep eutectic solvents (NADES). Sustainable Energy & Fuels, 4(4), 1891-1898.

183.     Araji, N., Madjinza, D. D., Chatel, G., Moores, A., Jérôme, F., & Vigier, K. D. O. (2017). Synthesis of maleic and fumaric acids from furfural in the presence of betaine hydrochloride and hydrogen peroxide. Green Chemistry, 19(1), 98-101.

184.     Mao, C., Zhao, R., Li, X., & Gao, X. (2017). Trifluoromethanesulfonic acid-based DESs as extractants and catalysts for removal of DBT from model oil. RSC advances, 7(21), 12805-12811. https://doi.org/10.1039/C6RA28448E

185.     Müller, C. R., Meiners, I., & de Maria, P. D. (2014). Highly enantioselective tandem enzyme–organocatalyst crossed aldol reactions with acetaldehyde in deep-eutectic-solvents. RSC Advances, 4(86), 46097-46101. https://doi.org/10.1039/C4RA09307K

186.     Omar, K. A., & Sadeghi, R. (2022). Physicochemical properties of deep eutectic solvents: A review. Journal of Molecular Liquids, 360, 119524. https://doi.org/10.1016/j.molliq.2022.119524

187.     Mulyono, S., Hizaddin, H. F., Alnashef, I. M., Hashim, M. A., Fakeeha, A. H., & Hadj-Kali, M. K. (2014). Separation of BTEX aromatics from n-octane using a (tetrabutylammonium bromide+ sulfolane) deep eutectic solvent–experiments and COSMO-RS prediction. Rsc Advances, 4(34), 17597-17606. https://doi.org/10.1039/C4RA01081G

188.     Huang, W., Wang, H., Hu, W., Yang, D., Yu, S., Liu, F., & Song, X. (2021). Degradation of polycarbonate to produce bisphenol A catalyzed by imidazolium-based DESs under metal-and solvent-free conditions. RSC advances, 11(3), 1595-1604. https://doi.org/10.1039/D0RA09215K

189.     Juneidi, I., Hayyan, M., & Hashim, M. A. (2015). Evaluation of toxicity and biodegradability for cholinium-based deep eutectic solvents. RSC Advances, 5(102), 83636-83647. https://doi.org/10.1039/C5RA12425E

190.     Cardellini, F., Germani, R., Cardinali, G., Corte, L., Roscini, L., Spreti, N., & Tiecco, M. (2015). Room temperature deep eutectic solvents of (1 S)-(+)-10-camphorsulfonic acid and sulfobetaines: Hydrogen bond-based mixtures with low ionicity and structure-dependent toxicity. RSC Advances, 5(40), 31772-31786. https://doi.org/10.1039/C5RA03932K

191.     Kali M.K.H., Khidir K.E.A., Wazeer I., Blidi L.E., Mulyono S., AlNashef I.M. (2015), Application of deep eutectic solvents and their individual constituents as surfactants for enhanced oil recovery, Col. Surfa. 487, 221-231. https://doi.org/10.1016/j.colsurfa.2015.10.005

192.     Sheldon, R. A. (2018). Metrics of green chemistry and sustainability: past, present, and future. ACS Sustainable Chemistry & Engineering6(1), 32-48. https://doi.org/10.1021/acssuschemeng.7b03505

193.     Nguyen, D., Van Huynh, T., Nguyen, V. S., Cao, P. L. D., Nguyen, H. T., Wei, T. C., ... & Nguyen, P. T. (2021). Choline chloride-based deep eutectic solvents as effective electrolytes for dye-sensitized solar cells. RSC advances, 11(35), 21560-21566. https://doi.org/10.1039/D1RA03273A

194.     Fan, K., Yang, B., Yu, S., Yang, R., Zhang, L., Chi, W., ... & Guo, J. (2023). Ternary choline chloride/benzene sulfonic acid/ethylene glycol deep eutectic solvents for oxidative desulfurization at room temperature. RSC advances, 13(37), 25888-25894. https://doi.org/10.1039/D3RA02524A

195.     Poliakoff, M., Fitzpatrick, J. M., Farren, T. R., & Anastas, P. T. (2002). Green chemistry: science and politics of change. Science297(5582), 807-810. https://doi.org/10.1126/science.297.5582.807

196.     Mulvihill, M. J., Beach, E. S., Zimmerman, J. B., & Anastas, P. T. (2011). Green chemistry and green engineering: a framework for sustainable technology development. Annual review of environment and resources36(1), 271-293. https://doi.org/10.1146/annurev-environ-032009-095500

197.     Tobiszewski, M., Marć, M., Gałuszka, A., & Namieśnik, J. (2015). Green chemistry metrics with special reference to green analytical chemistry. Molecules20(6), 10928-10946. https://doi.org/10.3390/molecules200610928

198.     Dai, Y., van Spronsen, J., Witkamp, G. J., Verpoorte, R., & Choi, Y. H. (2013). Natural deep eutectic solvents as new potential media for green technology. Anal. Chim. Acta, 766, 61-68. https://doi.org/10.1016/j.aca.2012.12.019

199.     Cunha, S. C., & Fernandes, J. O. (2018). Extraction techniques with deep eutectic solvents. TrAC Trends in Analytical Chemistry, 105, 225-239. https://doi.org/10.1016/j.trac.2018.05.001

200.     Chandran, D., Khalid, M., Walvekar, R., Mubarak, N. M., Dharaskar, S., Wong, W. Y., & Gupta, T. C. S. M. (2019). Deep eutectic solvents for extraction-desulphurization: A review. Journal of Molecular Liquids, 275, 312-322. https://doi.org/10.1016/j.molliq.2018.11.051

201.     Torregrosa-Crespo, J., Marset, X., Guillena, G., Ramón, D. J., & Martínez-Espinosa, R. M. (2020). New guidelines for testing “Deep eutectic solvents” toxicity and their effects on the environment and living beings. Science of the Total Environment, 704, 135382. https://doi.org/10.1016/j.scitotenv.2019.135382

202.     Pätzold, M., Siebenhaller, S., Kara, S., Liese, A., Syldatk, C., & Holtmann, D. (2019). Deep eutectic solvents as efficient solvents in biocatalysis. Trends in biotechnology, 37(9), 943-959.

203.     Laird, T. (2012). Green chemistry is good process chemistry. Organic Process Research & Development16(1), 1-2. https://doi.org/10.1021/op200366y

204.     Li, C. J., & Trost, B. M. (2008). Green chemistry for chemical synthesis. Proceedings of the National Academy of Sciences105(36), 13197-13202. https://doi.org/10.1073/pnas.0804348105

205.     Lei, Z., Chen, B., Koo, Y. M., & MacFarlane, D. R. (2017). Introduction: ionic liquids. Chemical Reviews, 117(10), 6633-6635. https://doi.org/10.1021/acs.chemrev.7b00246

206.     X. Zhao, G. Zhu, L. Jiao, F. Yu, C. Xie, Formation and extractive desulfurization mechanisms of aromatic acid based deep eutectic solvents: an experimental and theoretical study, Chem. Eur. J. 24 (2018) 11021–11032, https://doi.org/10.1002/chem. 201801631.

207.     Bjelić, A., Hočevar, B., Grilc, M., Novak, U., & Likozar, B. (2022). A review of sustainable lignocellulose biorefining applying (natural) deep eutectic solvents (DESs) for separations, catalysis and enzymatic biotransformation processes. Reviews in Chemical Engineering38(3), 243-272. https://doi.org/10.1515/revce-2019-0077

208.     Z. Li, D. Liu, Z. Men, L. Song, Y. Lv, P. Wu, B. Lou, Y. Zhang, N. Shi, Q. Chen, Insight into effective denitrification and desulfurization of liquid fuel with deep eutectic solvents: an innovative evaluation criterion to filtrate extractants using compatibility index, Green Chem. 20 (2018) 3112–3120, https://doi.org/10.1039/C8GC00828K

209.     H. Xu, D. Zhang, F. Wu, X. Wei, J. Zhang, Deep desulfurization of fuels with cobalt chloride-choline chloride/polyethylene glycol metal deep eutectic solvents, Fuel 225 (2018) 104–110, https://doi.org/10.1016/j.fuel.2018.03.159

210.     Ganesh, K. N., Zhang, D., Miller, S. J., Rossen, K., Chirik, P. J., Kozlowski, M. C., ... & Voutchkova-Kostal, A. M. (2021). Green chemistry: a framework for a sustainable future. Environmental Science & Technology55(13), 8459-8463. https://doi.org/10.1021/acs.est.1c03762

211.     T. Al-Wahaibi, Y. Al-Wahaibi, I.M. AlNashef, Deep oxidative desulfurization of liquid fuels, Rev. Chem. Eng. 30 (2014) 337–378, https://doi.org/10.1515/revce-2014-0001

212.     J.M. Campos-Martin, M.d.C. Capel-Sanchez, P. Perez-Presas, J. Fierro, Oxidative processes of desulfurization of liquid fuels, J. Chem. Technol. Biotechnol. 85 (2010) 879–890, https://doi.org/10.1002/jctb.2371

213.     Beach, E. S., Cui, Z., & Anastas, P. T. (2009). Green Chemistry: A design framework for sustainability. Energy & Environmental Science2(10), 1038-1049. https://doi.org/10.1039/B904997P

214.     Mbous, Y. P., Hayyan, M., Hayyan, A., Wong, W. F., Hashim, M. A., & Looi, C. Y. (2017). Applications of deep eutectic solvents in biotechnology and bioengineering—Promises and challenges. Biotechnology advances, 35(2), 105-134. https://doi.org/10.1016/j.biotechadv.2016.11.006

215.     Galiński, M., Lewandowski, A., & Stępniak, I. (2006). Ionic liquids as electrolytes. Electrochimica acta, 51(26), 5567-5580. https://doi.org/10.1016/j.electacta.2006.03.016

216.     Lima, F., Branco, L. C., Silvestre, A. J., & Marrucho, I. M. (2021). Deep desulfurization of fuels: Are deep eutectic solvents the alternative for ionic liquids?. Fuel, 293, 120297. https://doi.org/10.1016/j.fuel.2021.120297

217.     Pandey, S. (2006). Analytical applications of room-temperature ionic liquids: A review of recent efforts. Analytica chimica acta, 556(1), 38-45. https://doi.org/10.1016/j.aca.2005.06.038

218.     Merza, F., Fawzy, A., AlNashef, I., Al-Zuhair, S., & Taher, H. (2018). Effectiveness of using deep eutectic solvents as an alternative to conventional solvents in enzymatic biodiesel production from waste oils. Energy Reports, 4, 77-83. https://doi.org/10.1016/j.egyr.2018.01.005

219.     Berthod, A., Ruiz-Angel, M. J., & Carda-Broch, S. (2008). Ionic liquids in separation techniques. Journal of Chromatography A, 1184(1-2), 6-18. https://doi.org/10.1016/j.chroma.2007.11.109

220.     Anastas, P. T. (1999). Green chemistry and the role of analytical methodology development. Critical reviews in analytical chemistry29(3), 167-175. https://doi.org/10.1080/10408349891199356

221.     S.A. Dharaskar, K.L. Wasewar, M.N. Varma, D.Z. Shende, Imidazolium ionic liquid as energy efficient solvent for desulfurization of liquid fuel, Sep. Purif. Technol. 155 (2015) 101–109, https://doi.org/10.1016/j.seppur.2015.05.032

222.     W.N.A.W. Mokhtar, W.A.W.A. Bakar, R. Ali, A.A.A. Kadir, Deep desulfurization of model diesel by extraction with N,N-dimethylformamide: optimization by Box– Behnken design, J. Taiwan Inst. Chem. Eng. 45 (2014) 1542–1548, https://doi.org/10.1016/j.jtice.2014.03.017

223.     Paiva, A., Craveiro, R., Aroso, I., Martins, M., Reis, R. L., & Duarte, A. R. C. (2014). Natural deep eutectic solvents–solvents for the 21st century. ACS Sustainable Chemistry & Engineering, 2(5), 1063-1071. https://doi.org/10.1021/sc500096j

224.     Keskin, S., Kayrak-Talay, D., Akman, U., & Hortaçsu, Ö. (2007). A review of ionic liquids towards supercritical fluid applications. The Journal of Supercritical Fluids, 43(1), 150-180. https://doi.org/10.1016/j.supflu.2007.05.013

225.     Craveiro, R., Aroso, I., Flammia, V., Carvalho, T., Viciosa, M. T., Dionísio, M., ... & Paiva, A. (2016). Properties and thermal behavior of natural deep eutectic solvents. Journal of Molecular Liquids, 215, 534-540. https://doi.org/10.1016/j.molliq.2016.01.038

226.     Nian, B., & Li, X. (2022). Can deep eutectic solvents be the best alternatives to ionic liquids and organic solvents: A perspective in enzyme catalytic reactions. International journal of biological macromolecules, 217, 255-269. https://doi.org/10.1016/j.ijbiomac.2022.07.044

227.     W.S.A. Rahma, F.S. Mjalli, T. Al-Wahaibi, A.A. Al-Hashmi, Polymeric-based deep eutectic solvents for effective extractive desulfurization of liquid fuel at ambient conditions, Chem. Eng. Res. Des. 120 (2017) 271–283, https://doi.org/10.1016/j.cherd.2017.02.025

228.     Płotka Wasylka, J. De la Guardia, M., Andruch, V., & Vilková, M. (2020). Deep eutectic solvents V/S ionic liquids: Similarities and differences. Microchemical Journal, 159, 105539. https://doi.org/10.1016/j.microc.2020.105539

229.     Gordon, C. M. (2001). New developments in catalysis using ionic liquids. Applied Catalysis A: General, 222(1-2), 101-117. https://doi.org/10.1016/S0926-860X(01)00834-1

230.     C.-f. Mao, R.-x. Zhao, X.-p. Li, Phenylpropanoic acid-based DESs as efficient extractants and catalysts for the removal of sulfur compounds from oil, Fuel 189 (2017) 400–407, https://doi.org/10.1016/j.fuel.2016.10.113

231.     Cao, J., & Su, E. (2021). Hydrophobic deep eutectic solvents: The new generation of green solvents for diversified and colorful applications in green chemistry. Journal of Cleaner Production, 314, 127965. https://doi.org/10.1016/j.jclepro.2021.127965

232.     Perna, F. M., Vitale, P., & Capriati, V. (2020). Deep eutectic solvents and their applications as green solvents. Current Opinion in Green and Sustainable Chemistry, 21, 27-33. https://doi.org/10.1016/j.cogsc.2019.09.004

233.     Hou, Y. C., Yao, C. F., & Wu, W. Z. (2018). Deep eutectic solvents: green solvents for separation applications. Acta Phys.-Chim. Sin, 34(8), 873-885. doi: 10.3866/PKU.WHXB201802062

234.     R. Yusof, E. Abdulmalek, K. Sirat, M.B.A. Rahman, Tetrabutylammonium bromide (TBABr)-based deep eutectic solvents (DESs) and their physical properties, Molecules 19 (2014) 8011–8026, https://doi.org/10.3390/molecules19068011

235.     Welton, T. (2004). Ionic liquids in catalysis. Coordination chemistry reviews, 248(21-24), 2459-2477. https://doi.org/10.1016/j.ccr.2004.04.015

236.     Schuur, B., Brouwer, T., Smink, D., & Sprakel, L. M. (2019). Green solvents for sustainable separation processes. Current Opinion in Green and Sustainable Chemistry, 18, 57-65. https://doi.org/10.1016/j.cogsc.2018.12.009

237.     S.E. Warrag, I. Adeyemi, N.R. Rodriguez, I.M. Nashef, M. van Sint Annaland, M.C. Kroon, C.J. Peters, Effect of the type of ammonium salt on the extractive desulfurization of fuels using deep eutectic solvents, J. Chem. Eng. Data 63 (2018) 1088–1095. https://doi.org/10.1021/acs.jced.7b00832

238.     F. Lima, J. Gouvenaux, L.C. Branco, A.J. Silvestre, I.M. Marrucho, Towards a sulfur clean fuel: deep extraction of thiophene and dibenzothiophene using polyethylene glycol-based deep eutectic solvents, Fuel 234 (2018) 414–421, https://doi.org/10. 1016/j.fuel.2018.07.043

239.     K.H. Almashjary, M. Khalid, S. Dharaskar, P. Jagadish, R. Walvekar, T.C.S.M. Gupta, Optimisation of extractive desulfurization using Choline Chloride-based deep eutectic solvents, Fuel 234 (2018) 1388–1400, https://doi.org/10.1016/j.fuel.2018.08.005

240.     X.-L. Tang, L. Shi, Study of the adsorption reactions of thiophene on Cu (I)/HY-Al2O3 by Fourier transform infrared and temperature-programmed desorption: adsorption, desorption, and sorbent regeneration mechanisms, Langmuir 27 (2011) 11999–12007, https://doi.org/10.1021/la2025654

241.     Deplanche, K., Bennett, J. A., Mikheenko, I. P., Omajali, J., Wells, A. S., Meadows, R. E., ... & Macaskie, L. E. (2014). Catalytic activity of biomass-supported Pd nanoparticles: influence of the biological component in catalytic efficacy and potential application in ‘green’synthesis of fine chemicals and pharmaceuticals. Applied Catalysis B: Environmental, 147, 651-665. https://doi.org/10.1016/j.apcatb.2013.09.045

242.     D.V. Wagle, H. Zhao, C.A. Deakyne, G.A. Baker, Quantum chemical evaluation of deep eutectic solvents for the extractive desulfurization of fuel, ACS Sustain. Chem. Eng. 6 (2018) 7525–7531, https://doi.org/10.1021/acssuschemeng.8b00224

243.     S.E. Warrag, C. Pototzki, N.R. Rodriguez, M. van Sint Annaland, M.C. Kroon, C. Held, G. Sadowski, C.J. Peters, Oil desulfurization using deep eutectic solvents as sustainable and economical extractants via liquid-liquid extraction: experimental and PC-SAFT predictions, Fluid Phase Equilib. 467 (2018) 33–44, https://doi.org/10.1016/j.fluid. 2018.03.018

244.     H. Cheng, C. Liu, J. Zhang, L. Chen, B. Zhang, Z. Qi, Screening deep eutectic solvents for extractive desulfurization of fuel based on COSMO-RS model, Chem. Eng. Process. Process Intensif. 125 (2018) 246–252, https://doi.org/10.1016/j.cep.2018.02. 006

245.     R. Yusof, E. Abdulmalek, K. Sirat, M.B.A. Rahman, Tetrabutylammonium bromide (TBABr)-based deep eutectic solvents (DESs) and their physical properties, Molecules 19 (2014) 8011–8026, https://doi.org/10.3390/molecules19068011

246.     Liu, Y., Friesen, J. B., McAlpine, J. B., Lankin, D. C., Chen, S. N., & Pauli, G. F. (2018). Natural deep eutectic solvents: properties, applications, and perspectives. Journal of natural products, 81(3), 679-690. https://doi.org/10.1021/acs.jnatprod.7b00945

247.     Paiva, A., Craveiro, R., Aroso, I., Martins, M., Reis, R. L., & Duarte, A. R. C. (2014). Natural deep eutectic solvents–solvents for the 21st century. ACS Sustainable Chemistry & Engineering, 2(5), 1063-1071. https://doi.org/10.1021/sc500096j

248.     El-Deen, A. K., Elmansi, H., Belal, F., & Magdy, G. (2023). Recent advances in dispersion strategies for dispersive liquid–liquid microextraction from green chemistry perspectives. Microchemical Journal, 191, 108807. https://doi.org/10.1016/j.microc.2023.108807

249.     Z.S. Gano, F.S. Mjalli, T. Al-Wahaibi, Y. Al-Wahaibi, The novel application of hydrated metal halide (SnCl2.2H2O)-based deep eutectic solvent for the extractive desulfurization of liquid fuels, Int. J. Chem. Eng. Appl. 6 (2015) 367–371, https://doi.org/10. 7763/IJCEA.2015.V6.511

250.     W. Jiang, L. Dong, W. Liu, T. Guo, H. Li, S. Yin, W. Zhu, H. Li, Biodegradable cholinelike deep eutectic solvents for extractive desulfurization of fuel, Chem. Eng. Process. Process Intensif. 115 (2017) 34–38, https://doi.org/10.1016/j.cep.2017.02.004

251.     X. Wang, W. Jiang, W. Zhu, H. Li, S. Yin, Y. Chang, H. Li, A simple and cost-effective extractive desulfurization process with novel deep eutectic solvents, RSC Adv. 6 (2016) 30345–30352, https://doi.org/10.1039/C5RA27266A

252.     W.S.A. Rahma, F.S. Mjalli, T. Al-Wahaibi, A.A. Al-Hashmi, Polymeric-based deep eutectic solvents for effective extractive desulfurization of liquid fuel at ambient conditions, Chem. Eng. Res. Des. 120 (2017) 271–283, https://doi.org/10.1016/j.cherd. 2017.02.025

253.     C.-f. Mao, R.-x. Zhao, X.-p. Li, Phenylpropanoic acid-based DESs as efficient extractants and catalysts for the removal of sulfur compounds from oil, Fuel 189 (2017) 400–407, https://doi.org/10.1016/j.fuel.2016.10.113

254.     Bolivar, J. M., Woodley, J. M., & Fernandez-Lafuente, R. (2022). Is enzyme immobilization a mature discipline? Some critical considerations to capitalize on the benefits of immobilization. Chemical Society Reviews, 51(15), 6251-6290. https://doi.org/10.1039/D2CS00083K

255.     Chang, X. X., Mubarak, N. M., Mazari, S. A., Jatoi, A. S., Ahmad, A., Khalid, M., ... & Nizamuddin, S. (2021). A review on the properties and applications of chitosan, cellulose and deep eutectic solvent in green chemistry. Journal of industrial and engineering chemistry, 104, 362-380. https://doi.org/10.1016/j.jiec.2021.08.033

256.     Ge, X., Gu, C., Wang, X., & Tu, J. (2017). Deep eutectic solvents (DESs)-derived advanced functional materials for energy and environmental applications: challenges, opportunities, and future vision. Journal of Materials Chemistry A, 5(18), 8209-8229. https://doi.org/10.1039/C7TA01659J

257.     Horváth, I. T., & Anastas, P. T. (2007). Innovations and green chemistry. Chemical reviews107(6), 2169-2173. https://doi.org/10.1021/cr078380v

258.     Ahsan, H., Islam, S. U., Ahmed, M. B., Lee, Y. S., & Sonn, J. K. (2020). Significance of green synthetic chemistry from a pharmaceutical perspective. Current Pharmaceutical Design, 26(45), 5767-5782. https://doi.org/10.2174/1381612826666200928160851

259.     Anastas, P. T., & Williamson, T. C. (1996). Green chemistry: an overview. DOI; 10.1021/bk-1996-0626.ch001

260.     Sheldon, R. A. (2017). The E factor 25 years on: the rise of green chemistry and sustainability. Green Chemistry, 19(1), 18-43. https://doi.org/10.1039/C6GC02157C

261.     Clark, J. H., Farmer, T. J., Herrero-Davila, L., & Sherwood, J. (2016). Circular economy design considerations for research and process development in the chemical sciences. Green Chemistry, 18(14), 3914-3934. https://doi.org/10.1039/C6GC00501B

262.     Clarke, C. J., Tu, W. C., Levers, O., Brohl, A., & Hallett, J. P. (2018). Green and sustainable solvents in chemical processes. Chemical reviews, 118(2), 747-800. https://doi.org/10.1021/acs.chemrev.7b00571

263.     Iravani, S. (2011). Green synthesis of metal nanoparticles using plants. Green chemistry13(10), 2638-2650. https://doi.org/10.1039/C1GC15386B

264.     Hessel, V., Tran, N. N., Asrami, M. R., Tran, Q. D., Long, N. V. D., Escribà-Gelonch, M., ... & Sundmacher, K. (2022). Sustainability of green solvents–review and perspective. Green Chemistry, 24(2), 410-437. https://doi.org/10.1039/D1GC03662A

265.     Anastas, P., & Eghbali, N. (2010). Green chemistry: principles and practice. Chemical Society Reviews, 39(1), 301-312. https://doi.org/10.1039/B918763B

266.     Bhagwat, P., Amobonye, A., Singh, S., & Pillai, S. (2022). Deep eutectic solvents in the pretreatment of feedstock for efficient fractionation of polysaccharides: current status and future prospects. Biomass Conversion and Biorefinery, 12(Suppl 1), 171-195. https://doi.org/10.1007/s13399-021-01745-x

267.     Aziz, M. A. A., Jalil, A. A., Triwahyono, S., & Ahmad, A. (2015). CO 2 methanation over heterogeneous catalysts: Recent progress and future prospects. Green Chemistry, 17(5), 2647-2663. https://doi.org/10.1039/C5GC00119F

268.     Mostafazadeh, A. K., Karimiestahbanati, M., Diop, A., Adjallé, K., Drogui, P., & Tyagi, R. D. (2021). Green Chemistry for Green Solvent Production and Sustainability Toward Green Economy. In Biomass, Biofuels, Biochemicals (pp. 583-636). Elsevier https://doi.org/10.1016/B978-0-12-821878-5.00017-9

269.     M.K. Hadj-Kali, S. Mulyono, H.F. Hizaddin, I. Wazeer, L. El-Blidi, E. Ali, M.A. Hashim, I.M. AlNashef, Removal of thiophene from mixtures with n-heptane by selective extraction using deep eutectic solvents, Ind. Eng. Chem. Res. 55 (2016) 8415–8423, https://doi.org/10.1021/acs.iecr.6b01654

270.     C. Li, J. Zhang, Z. Li, J. Yin, Y. Cui, Y. Liu, G. Yang, Extraction desulfurization of fuels with ‘metal ions’ based deep eutectic solvents (MDESs), Green Chem. 18 (2016) 3789–3795, https://doi.org/10.1039/C6GC00366D

271.     S.E. Warrag, N.R. Rodriguez, I.M. Nashef, M. van Sint Annaland, J.I. Siepmann, M.C. Kroon, C.J. Peters, Separation of thiophene from aliphatic hydrocarbons using tetrahexylammonium-based deep eutectic solvents as extracting agents, J. Chem. Eng. Data 62 (2017) 2911–2919, https://doi.org/10.1021/acs.jced.7b00168

272.     T. Khezeli, A. Daneshfar, Synthesis and application of magnetic deep eutectic solvents: novel solvents for ultrasound assisted liquid-liquid microextraction of thiophene, Ultrason. Sonochem. 38 (2017) 590–597, https://doi.org/10.1016/j. ultsonch.2016.08.023

273.     H.F.M. Zaid, F.K. Chong, M.I.A. Mutalib, Extractive deep desulfurization of diesel using choline chloride-glycerol eutectic-based ionic liquid as a green solvent, Fuel 192 (2017) 10–17, https://doi.org/10.1016/j.fuel.2016.11.112

274.     J.M. Campos-Martin, G. Blanco-Brieva, J.L. Fierro, Hydrogen peroxide synthesis: an outlook beyond the anthraquinone process, Angew. Chem. Int. Ed. 45 (2006) 6962–6984, https://doi.org/10.1002/anie.200503779

275.     J. Yin, J. Wang, Z. Li, D. Li, G. Yang, Y. Cui, A. Wang, C. Li, Deep desulfurization of fuels based on an oxidation/extraction process with acidic deep eutectic solvents, Green Chem. 17 (2015) 4552–4559, https://doi.org/10.1039/C5GC00709G

276.     H. Lü, P. Li, C. Deng, W. Ren, S. Wang, P. Liu, H. Zhang, Deep catalytic oxidative desulfurization (ODS) of dibenzothiophene (DBT) with oxalate-based deep eutectic solvents (DESs), Chem. Commun. 51 (2015) 10703–10706, https://doi.org/10.1039/c5cc03324a

277.     M. Zhang, W. Zhu, S. Xun, H. Li, Q. Gu, Z. Zhao, Q. Wang, Deep oxidative desulfurization of dibenzothiophene with POM-based hybrid materials in ionic liquids, Chem. Eng. J. 220 (2013) 328–336, https://doi.org/10.1016/j.cej.2012.11.138

278.     Y. Nie, X. Gong, H. Gao, X. Zhang, S. Zhang, Simultaneous desulfurization and denitrogen of liquid fuels using two functionalized group ionic liquids, Sci. China Chem. 57 (2014) 1766–1773, https://doi.org/10.1007/s11426-014-5164-1

279.     L. Hao, M. Wang, W. Shan, C. Deng, W. Ren, Z. Shi, H. Lü, L-proline-based deep eutectic solvents (DESs) for deep catalytic oxidative desulfurization (ODS) of diesel, J. Hazard. Mater. 339 (2017) 216–222, https://doi.org/10.1016/j.jhazmat.2017.06.050

280.     Y. Nie, Y. Dong, L. Bai, H. Dong, X. Zhang, Fast oxidative desulfurization of fuel oil using dialkylpyridinium tetrachloroferrates ionic liquids, Fuel 103 (2013) 997–1002, https://doi.org/10.1016/j.fuel.2012.07.071

281.     H. Lü, P. Li, Y. Liu, L. Hao, W. Ren, W. Zhu, C. Deng, F. Yang, Synthesis of a hybrid Anderson-type polyoxometalate in deep eutectic solvents (DESs) for deep desulphurization of model diesel in ionic liquids (ILs), Chem. Eng. J. 313 (2017) 1004–1009, https://doi.org/10.1016/j.cej.2016.10.140

282.     W. Liu, W. Jiang, W. Zhu, W. Zhu, H. Li, T. Guo, W. Zhu, H. Li, Oxidative desulfurization of fuels promoted by choline chloride-based deep eutectic solvents, J. Mol. Catal. A Chem. 424 (2016) 261–268, https://doi.org/10.1016/j.molcata.2016.08.030

283.     E. A. Krisanti, K. Saputra, M.M. Arif, K. Mulia, (2019), Formulation and characterization of betaine-based deep eutectic solvent for extraction phenolic compound from spent coffee grounds, AIP Conf. Proc. 2175, 020040-020048. https://doi.org/10.1063/1.5134604

284.     Llovell Ferret, F. L., Alkhatib, I. I., Ferreira, M. L., Alba, C. G., Bahamon, D., Pereiro, A. B., ... & Vega, L. F. (2020). Screening of ionic liquids and deep eutectic solvents for physical CO2 absorption by soft-SAFT using key performance indicators. J. Chem. Eng. Data. 65, 12, 5844-5861. https://doi.org/10.1021/acs.jced.0c00750

285.     D.V.Wagle, H. Zhao, C.A. Deakyne, G.A. Baker, Quantum chemical evaluation of deep eutectic solvents for the extractive desulfurization of fuel, ACS Sustain. Chem. Eng. 6 (2018) 7525–7531, https://doi.org/10.1021/acssuschemeng.8b00224

286.     Florindo C., Oliveira F.S., Rebelo L.P.N., Fernandes A.M., Murrucho I.M., (2014), Insights into the Synthesis and Properties of Deep Eutectic Solvents Based on Cholinium Chloride and Carboxylic Acids, ACS Sustainable Chem.Eng. 10, 2416-2425. https://doi.org/10.1021/sc500439w

287.     El Achkar, T., Greige-Gerges, H., & Fourmentin, S. (2021). Basics and properties of deep eutectic solvents: a review. Environmental chemistry letters, 19, 3397-3408. https://doi.org/10.1007/s10311-021-01225-8

288.     Abranches, D. O., & Coutinho, J. A. (2022). Type V deep eutectic solvents: Design and applications. Current Opinion in Green and Sustainable Chemistry, 35, 100612. https://doi.org/10.1016/j.cogsc.2022.100612

289.     Janicka, P., Kaykhaii, M., Płotka-Wasylka, J., & Gębicki, J. (2022). Supramolecular deep eutectic solvents and their applications. Green Chemistry, 24(13), 5035-5045. https://doi.org/10.1039/D2GC00906D

290.     El Achkar, T., Greige-Gerges, H., & Fourmentin, S. (2021). Understanding the basics and properties of deep eutectic solvents. Deep Eutectic Solvents for Medicine, Gas Solubilization and Extraction of Natural Substances, 1-40. https://doi.org/10.1007/978-3-030-53069-3_1

291.     Sas, O.G.; Domínguez, I.; González, B. Liquid-liquid extraction of phenolic compounds from water using ionic liquids: Literature review and new experimental data using [C2mim]FSI. J. Environ. Manag. 2018, 228, 475–482. https://doi.org/10.1016/j.jenvman.2018.09.042

292.     Sas, O.G.; Sánchez, P.B.; González, B. Removal of phenolic pollutants from wastewater streams using ionic liquids. Sep. Purif. Technol. 2019, 236, 116310. https://doi.org/10.1016/j.seppur.2019.116310

293.     Wang, Y.; Wang, X.; Li, H. Treatment of high salinity phenol-laden wastewater using a sequencing batch reactor containing halophilic bacterial community. Int. Biodeterior. Biodegrad. 2014, 93, 138–144. https://doi.org/10.1016/j.ibiod.2014.04.010

294.     Raza, W.; Lee, J.; Raza, N. Removal of phenolic compounds from industrial waste water based on membrane-based technologies.J. Ind. Eng. Chem. 2019, 71, 1–18. https://doi.org/10.1016/j.jiec.2018.11.024

295.     Tri NL, M.; Thang, P.Q.; Tan, L.V.; Tahtamouni, T.M.A. Removal of phenolic compounds from wastewaters by using synthesized Fe-nano zeolite. J. Water Process. Eng. 2020, 33, 101070. https://doi.org/10.1016/j.jwpe.2019.101070

296.     Alshabib, M.; Onaizi, S.A. A review on phenolic wastewater remediation using homogeneous and heterogeneous enzymatic processes: Current status and potential challenges. Sep. Purif. Technol. 2019, 219, 186–207. https://doi.org/10.1016/j.seppur.2019.03.028

297.     Rispail, N.; Morris, P.;Webb, K.J. Phenolic compounds extraction and analysis. In Lotus Japonicus Handbook; Márquez, A.J., Ed.; Springer: Amsterdam, The Netherlands, 2005; pp. 349–354. https://doi.org/10.1007/1-4020-3735-X_34

 

 



Related Images:

Recomonded Articles:

Author(s): Lavkesh Kumar Singh Tanwar; Kallol K Ghosh

DOI: 10.52228/JRUB.2024-37-1-5         Access: Open Access Read More

Author(s): Benvikram Barman; Manoj Kumar Banjare; Bhupendra Singh Banjare; Dolly Baghel

DOI: 10.52228/JRUB.2025-38-1-7         Access: Open Access Read More

Author(s): Deepti Tikariha; Jyotsna Lakra; Srishti Dutta Roy; Toshikee Yadav; Kallol KGhosh

DOI:         Access: Open Access Read More

Author(s): Sanmoy Karmakar

DOI:         Access: Open Access Read More

Author(s): Renu Bhatt; Neha Pandey

DOI:         Access: Open Access Read More

Author(s): PR Shende; PR Itankar; SK Prasad

DOI:         Access: Open Access Read More

Author(s): Kallol K. Ghosh; Kishor K. Krishnan

DOI:         Access: Open Access Read More

Author(s): Bina Gidwani; Amber Vyas; Chanchal Deep Kaur

DOI:         Access: Open Access Read More

Author(s): Kallol K.Ghosh; Klshoae K Krishnanl

DOI:         Access: Open Access Read More

Author(s): Sonam S Gonnade; PR Itankar; SK Prasad

DOI:         Access: Open Access Read More

Author(s): Subrat Verma; Shobhana Ramteke; Manas Kanti Deb

DOI: 10.52228/JRUB.2025-38-1-14         Access: Open Access Read More