Open access peer-reviewed chapter

Green Solvents

Written By

Parul Tomar and Deepali Jain

Submitted: 20 July 2023 Reviewed: 27 July 2023 Published: 25 August 2023

DOI: 10.5772/intechopen.1002491

From the Edited Volume

Solvents - Dilute, Dissolve, and Disperse - Insights on Green Solvents and Distillation

Raffaello Papadakis and Vilmar Steffen

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Abstract

Prolonged use of solvents has harmful impacts on the environment, and entire surviving things. One of the most crucial demands of green chemistry is the cutting down of solvent use or substituting with less hazardous ones. Green solvents are explored as an alternative to traditional solvents. They are specified by low toxicity, easy availability re-usability extraordinary efficiency, environmentally friendly reaction medium, non-flammability, increased reactions rate, decrease reaction temperatures as well greater selectivity, and non-volatility. There are numerous applications of green solvents in many industries such as the cosmetic, pharmaceutical industries, chemical industries, perfumery, and also expended to extract crude material, flavonoids, oils and fats, scents and antioxidants, proteins, volatile compounds, and sugars. To get over the properly-hooked up drawbacks of traditional solvents, exquisite extraordinary research attempts have been these days dedicated to the alternative of conventional chemical reaction media using the so-known as green Solvents. In this experience, the selection of a secure, bio-renewable, non-toxic, and reasonably-priced response media is a vital purpose in chemical synthesis. Thus, this special issue on “green solvents” has been aimed to show off a sequence of exhilarating contributions from global researchers within the various sub-regions of chemical synthesis in green solvents.

Keywords

  • green chemistry
  • green solvents
  • ionic liquids (ILs)
  • water
  • deep eutectic solvents (DESs)
  • supercritical fluids
  • extraction
  • catalysis

1. Introduction

Traditional chemical employment imparts to huge quantity of health and environmental hazards. To scale down these hazards and for accomplishing more environmentally friendly outcomes, the research for alternate options has always been the field of concern. Green chemistry is base for potential alternatives accommodating to the future of chemical industrialization. It is the novel springing up an area that to get the property of being sustainable (sustainability) endeavors to exploit at the stage of molecular extent. According to reports, the field exhibits the capability of safe chemical inventions to accomplish economical and environmental aims. At the opening of the 1990s, a close manner, 20 years ago, the conception of green chemistry has been first invented. It has been defined as the intention of chemical substances and procedures to scale down or get rid of the usage and production of dangerous materials. Green chemistry has assigned a set of 12 principles. These principles approach as a directing framework to the synthesis of noble chemicals regarding holistic access towards green technological development with safety, economy, and biodegradability [1, 2, 3].

The 12 principles of green chemistry are summed up under [1]:

  1. Nonproliferation: Reducing waste before it multiplies is preferable to removing it afterwords it has been produced

  2. Atomic efficiency: Total crude substances should be contained in the very last compounds using synthetic techniques.

  3. Involving low risk or dangerous compounds Synthesis: Whensoever possible, it is necessary to choose techniques with minimal negative effects on the surroundings and human beings.

  4. Formulating secure chemical substances: Chemicals must be made in a way that preserves the reactions’ usefulness while reducing their hazard.

  5. More risk free solvents and supporters: It is important to avoid using auxiliary substances wherever possible, and when they are utilized, they must be used sparingly.

  6. Invention for energy economy: Energy effect requirements on the surroundings must be identified, and if possible, they should be reduced or changed.

  7. Utilize sustainable raw materials: As executable, crude substances should be recyclable as opposed to consume.

  8. Step-down derivatives: The production of derivatives ought to be derogated as well as nullified, when viable, and demands extra chemicals and may result in waste.

  9. Catalyst: Using catalytic chemicals instead of stoichiometric ones can ameliorate reaction efficacy and decrease energy demand.

  10. Planning for degeneration: Chemicals applied must be able to smash down after the reaction in less difficult bio-decomposable substances by response and cease remaining in surroundings

  11. Real-time evaluation for contamination interference: Evaluation techniques ought be advanced to allow real-time, procedure observation as well as manipulation dangerous materials prior to production.

  12. Implicitly sounder chemistry for accidental injury avoidance: materials for compounds synthesis processes need to prefer for reducing whatever type of chemical injury which includes explosions, and fires

Challenges have surfaced in the sector of chemical treatment due to the daily use of massive quantities of hazardous and combustible solvents. More than 20 million tonnes of organic solvent waste wastes are released into the air every year, resulting in wasteful solvent wastage and environmental pollution. Dimethyl sulfoxide (DMSO), dimethyl formamide (DMF), acetone, and aromatic solvents like benzene, toluene, and chlorinated solvents (CHCl) are examples of organic solvents that contribute to ecosystem contamination but are still widely used. All systems found in living beings are adversely affected by persistent interaction with solvents, but the respiratory and neurological systems are particularly vulnerable. Additionally, the use of dangerous solvents is harmful to organs, for example, chloroform and carbon tetrachloride are hepatotoxic. Glycol ethers and chlorine-based solvents are employed when renal damage arises.

Additionally, dealing with particular chemicals, such as diethylene glycol (DEG), petrochemical distillates, and halogen-containing hydrocarbons, can cause kidney tubular necrosis even quickly. The World Health Organization (WHO) reports that a quarter of all current diseases are caused by prolonged exposure to environmental contaminants. The contaminants accumulate to hazardous levels as a result of the release of manmade compounds or an overabundance of naturally occurring substances. High pollution levels threaten human health, reduce the diversity of species, and damage ecological systems. One of the most significant objectives for sustainable chemistry is to apply fewer solvents or to replace them with ones that are less harmful.

The aforementioned information is of tremendous interest to both academics and industry regarding the usage of environmentally conscious solvents [4, 5, 6, 7, 8, 9, 10].

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2. Traditional solvents and their hazards

Traditional solvents are common laboratory solvents that we use every day for industrial purposes as well as for laboratory because of their melting point, volatility, better dissolution power, and yield. Aside from their addressed influence on lab workers, when liberated in surroundings such as air, soil, and water, these can induce strong threats to plants, human beings, and animals from the bottom level attaining to the bulk level when leftover untreated [11]. Most of the chemicals are dangerous if not managed cautiously. Direct interaction with the skin, breathing, and eye contact and extended, and exposure are the two of greater importance path of chemical perniciousness to mankind. Damaging to health, harm to organs, breaking of the immune system, growth of allergies, respiratory disorders, generative disturbs and congenital abnormality, effects on the mental condition and intellect or physiological growth of children, cancer, etc. can rely on the chemical substance constitution [12].

According to the Team for European Solvents Commercial Enterprise recommendation for following European Union (EU) regulations ameliorate atmosphere attribute via encouraging step-down entire volatile organic compounds (VOCs) release after 1990s [13]. Unyielding chemicals deposition inside surroundings, and fallaciously unwanted materials treatment are base reason for environs contamination for a period and stimulates serious toxicity to the earth, atmosphere, and water body [14]. Ozone layer depletion, land and water pollution, biological oxygen demand (BOD), and chemical oxygen demand (COD) are the most crucial consequences of extensive expenditure on traditional solvents. The Solvents Industry Association provides proposals and instructions to manufacturers, suppliers as well as exploiters of solvents to facilitate derogating potential environmental strikes [15]. Industry and producing corporations usually depend on solvents for a large number of works like manufacturing products, scavenging and getting rid of grease or oil from surfaces and machinery, exploiting chemicals that aid in chemical reactions, like paints, and coatings. In order to reduce the utilization of organic volatile solvents with having negative effects on human health and the environment, various organizations with sustainability programmes are searching for environmental amicable resolutions. Different conventional solvents, their sources, and related risks to human health and the environment.

Utilizing reusable solvents and incineration, two balancing techniques can be used to reformulate energy. Distillate is used in the refinement of used solvents, which uses more energy than producing new solvents to a comparable degree. Energy is directly produced by incinerating waste, although this process necessitates the production of additional solvent locally. The approach that provides the greatest cumulative energy demand (CED) discount is dependent upon the type of solvent.

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3. Definition of green solvents

In the headline of their 2007, Capello and Fischer [16] have posed the query at ETH Zurich (in any other case called as a Swiss Federal Institute Technology) is an elementary; “what is a green solvent”? Their reply may be considered like a fast life cycle assessment (LCA) kind estimation and now is prestigious, cuckold environmental evaluation, guard, welfare, and energy requirement. After recognizing the energy demanded to develop solvents, and the alternatives to be had at quit-of-existence to retrieve some of that energy, the ultimate CED for solvent manufacturing can be figured out. Utilizing reusable solvents and incineration, two balancing techniques can be used to reformulate energy. Distillate is habituated in the refinement of applied solvents, which consume more energy than manufacturing latest solvents to a comparable extent. Incinerating wastes straightforwardly results in energy, although this procedure calls for the manufacture of surplus solvents topically. Method which gives more CED discount is reckoned upon the kind of solvents. The energy for distillation of a solvent is lesser than produced. The incineration credit is the energy retrieval from combustion, yielding a discounted CED. According to modified LCA admittance, most (however no longer all) hydrocarbons are great incinerated for example n-hexane however no longer toluene, and the identical enforces to diethyl ether. The functionalized solvents with more lifelong manufacturing ways are quality recycled to hold the energy and merit invested into the molecules throughout their authentic synthesis for example DMF, and blessings for ethyl alcohol are rather evenly distributed. The same authors have produced still more precise elaborated valuation of energy call for solvents output [17].

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4. Uses, sources, and types of green solvents

Solvents employed in one-of-a-kind chemical procedures are determined to fundamental sustainability challenges [4]. Yearly boom records have reported that mass of chemical manufacturing enterprise through Europe has anticipated for booming by 3.1% showing greater participation, contributing to environmental reduction [18]. Thus, step-down the employment of solvents, and substituting these with low poisonous greener dissolvents are two main goals for sustainable chemistry [19].

Fisher asserts that the greener solvents press out a target for diminishing in the atmospheric effect of solvent intake in chemical manufacturing [20, 21]. Efficient exercise of green solvents consisting of water, ionic liquids (ILs), supercritical fluids, and liquid polymers can assist reap the objective to cut down environmental depletion. Low harmfulness, section conduct, chemicals, thermodynamics, non-flammability, and biodegradation are some of the homes of novel biosolvents or green solvents [22]. And indicates one-of-a-kind sorts of green solvents at the side of their respective examples and discusses unique solvents their sources, commercial, and standard makes use of.

In the separation of terpenes, plant based substances and oils serve as a terrific alternative to petrochemical solvents such as n-hexane [23]. Water, existing as a worldwide greener media and not-poisonous, may be utilized inside numerous response mediums, separation, extraction, and chemical formations [24]. Deep eutectic solvents (DESs) are some other environmentally beneficial green solvent that are extensively applied during diffusive liquid–liquid based microextraction [25], and ecological absorbent materials for risky chemical contaminants [26]. Some other amazing magnificence categories of green solvents admit ILs, that are utilized in commercial settings exploited in getting rid from sulfur from petroleum-based products [27] and carbon absorption [28]. Rather than utilization of n-hexane, n-butane may be consumed to serve as an attainable solvent during plant-based materials isolation [29]. In processor for polymers melting [30] and prior-remedy of lignin-based biomass [31]. Super-critical liquids are another class of green solvents that can be the best alternative to conventional solvents. Fatty acid esters are a good desired as a solvent components for carotenoid extraction [32]. Bioethanol, due to its low toxicity and constant obtainability, is habituated as a green solvent in numerous synthesizes and the industry manufactures [33]. Because of its renewability, easy decomposition, cost-effective, and eco-friendly, castor oil functions as auspicious green solvent for nanoparticles synthesis [34], agriculture, meals, fabric, papers, plastics, rubber, cosmetics, perfumes, coatings, electronics, pharmaceutics, paints, additives, ink, lubricating substance, and biofuels [35].

Bio-derived specially solvents which include ethyl lactate also are a sustainable solvent in the treatment of green tea biomolecules [36] as well as in the chemical reactions notably and in synthesis [37]. Polyethylene glycol (PEG) is also a green alternative that is widely known for its carbon–carbon bond-making and coupling reactions [38].

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5. Synthesis schemes with green solvents

In all product formation procedures and distinct applications in industry, solvents are wanted in large quantities resulting in ample quantities of waste. Path-breaking technologies and distinct synthesis strategies have been discoursed solventless operations that are not admitted for every field of study because of a few marketplace issues. Later on solventless thoughts, chemists as well as medicinal scientists investigated solvents that fit green chemistry. Fischer has reported that green solvents explicitly have the objective to reduce the environmental effect triggered by the intake of chemicals throughout manufacturing [21]. For solvents that are considered greener, certain techniques have been merged. The following are alternatives to dangerous solvents that are extra kinder to the planet, recyclable, and downplaying for ozone layer exhaustion potency, habituation of bio-solvents or oleochemicals, and replacement of organic solvents which are ILs, and supercritical fluids.

According to the literature review, various examples of green solvents can be visible for cooking natural products, drugs, and crucial intermediate productions which can be applied to foster synthesis [16].

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6. Ionic liquids as green solvents

Magical chemical substance ILs, having precisely tunable houses with loads of packages applications in each area have arrested brilliant attraction from scientists universally. The history of liquids efficiently commenced in 1914 while the beginning of the early IL ethyl ammonium nitrate [EtNH3] [NO3], having a melting state of 12°C has been reported. Later on, a progression of first-rate associated ILs have been exposed remarkably, have demonstrated tremendous pursuit within the chemicals industries as well as in academical due to their amazing greener dimensions and pose as a liquid at beneath a 100°C temperature. ILs do not have any borderline between inorganic and organic compounds due to their tunable characteristics. Additionally, goal-specified ILs with adjustable properties can be fashioned using converting cation-anion combining. Examples of various ordinarily devoted cationic parts are pyridinium [39], imidazolium [40], ammonium [41], pyrrolidinium [42], phosphonium [43], and piperidinium [44] with version constituents and anionic substituents tetrafluoroborates, alkyl sulphonates, alkyl tosylates, and hexafluorophosphates for manufacturing of ILs. As an end outcome, ILs have very much blessings over conventional organic solvents consisting of magnificently down volatility, worthless vapor strain [45], less dangerous, non-flammability [46], dissolubility, and greater.

Environment compatible, viscosity [47], excessive chemical as well as thermal stability [48], and eminent ionic conductance [49, 50, 51, 52]. Ordinarily, the viscosity of ILs swears by and complements with growing hydrogen bondings, the forces produced by van der Waals, hydrocarbon chains dimensions, along with the volume comprising fluorinations and anions. Moreover, ILs usually have a viscosity that fluctuates between 10 and 500 mPa at ambient temperature [53, 54, 55, 56].

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7. Ionic liquids as ionic salts

ILs are tremendously wonderful and different from ionic salts like NaCl [57]. Ionic salts lie in a solid state at room temperature and also have electrostatics interplay with generally metal cations and non-metal anions.

Wholely, ionic substances inclusive of NaCl can be in a molten or liquid phase at excessive temperatures. Therefore, ionic salts are incapable of being applied to the establishment of organic compounds. Where, ILs, a class of ionic salts with a melting state beneath 100°C, can be beneficial for chemical synthesis due to their ability to dissolve in inorganic, organometallic, and organic materials [58].

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8. Water as green solvent

Water exhibits numerous peculiar physicals and chemical homes including massive hydrogen bonding, excessive heat potentiality, big dielectric steady, and a big temperature range. Water as a universal solvent has consequently lots of benefits over traditional solvents. Moreover water can be decided on as a green solvent because of its cost-effectiveness, no trouble to be handled, safe, no risk, nonpolluting, and easy as well as quickly obtainable, and inflammable. As a matter of fact, human beings do not address water to be known as a chemical. Despite a large number of crucial benefits of water, it’s far still no longer usually applied to be known as a sole solvent for synthesis schemes in laboratories and industries as the maximum of the chemical components do not have the property of being dissoluble throughout water. Since water has been the medium of preference for our planet’s biochemical processes for hundreds of years, researchers are striving to replicate the inherent synthesis procedures that occur in water. As a consequence of an antique scientific hypothesis that claims irreducibly undissolved chemicals can not anymore produce any kind of substance, investigators found themselves off out of the water during a significant amount of time. Simultaneously, Sharpless has changed such superannuated concept by branded novel wondering thoughts such responses must be advanced “along” or “inside” water, by proposing that dissolvability is not vital to chemical responses. Sharpless has discovered procedures inclusive of cycloadditions, nucleophilic establishing of epoxides, Diels-Alders, and Claisen rearrangements in that as the reactants had been not dissolved in water, the reactions were described as being on-water [59].

Despise the fact that water reasons many issues as a solvent in chemical synthesis, purification processes, and separation of end products, Recently, it has been turned very much preferred in organic reactions. In a few instances, water accelerates reactions by dissolving the reagents and guarantees selectivity. Furthermore, oxygen can not be dissolved in water which may be a bonus for metallic catalysts. In the closing decade water has grown to be an actually beloved solvent encourages of its characteristics which include being nonhazardous for the natural world and has been authenticated in a bombastic quantity of papers [60, 61, 62]. It has been acknowledged that water is the most addictive solvent in every biochemistry reaction conveyed in nature [61]. Nevertheless, water is an appropriate solvent only for organic reactions, having polar groups such as carboxylic acids or alcohols. Notwithstanding, two centuries ago unique selectivity existed in aqueous solvents, and was additionally located in water suspensions, when one dissoluble component interacted with a badly dissoluble one [5, 61, 63]. Recently, various scientists have discovered an awesome speedup of chemical processes in this sort of suspension, assigned by them: reactions on water. It could be a statement to mention that water is exactly an eco-friendly solvent, it dominates notable homes which are substantially precise, related to the hydrophobic phenomenon [59, 61, 63, 64].

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9. Deep eutectic solvents as green solvents

Firstly Abbott et al. have defined DES [65] in the context of a sustainable solvent-based combination of choline chloride together with urea an example of, whilst combined in an adequate mole ratio, demonstrated meltdown factors lots below compared to the values of any one particular part of many constituents. The term ‘eutectic’ arises from the Greek word ευτηκτoς, interpreted as easily melting’, and in 1884, British investigator Guthrie [66] utilized it for elucidating a lesser degree for the liquefying compared to specified by existing proportionality. In the future, it becomes crucial to keep in mind, nevertheless, in which just a few eutectic combinations deserve to be designated as DES since, hardly every combo of substances which remain insoluble inside a stable segment necessarily demonstrate an eutectic state, as pointed out throughout the discussion through Martins et al. [67]. According to International Journal of Molecular Science, 2022, for the qualifying word ‘deep’, to date, there is no cosmically harmonized clarification, however maximum of the litterateurs coined the word ‘deep’ as those mixtures with a eutectic temperature some distance beneath that of a model liquid solution [68, 69, 70]. Even though distinct appellations are exploited, the precept implemented to categorize DES is identical and the DES acronym is still utilized in an always globalizing idea. Smith et al. [71] recalled the word ‘deep eutectic’ to encompass the eutectic combination of Brønsted or Lewis acids as well as bases which contain more than a few cationic and anionic species and categorized them into four distinct kinds because of their materials [71]. Particularly, DES can be specified by an arrangement of one or more hydrogen bonds donator (HBD) as well as hydrogens bonds admittance chemical substances those, with a proper mole proportions, display an eutectic state temperatures under those for an outstanding solutions [67, 68, 69, 70].

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10. Peculiar physicochemical characteristics of deep eutectic solvents

The fascinating consequence demonstrated through DES is that solid pure constituents can get liquid via intermixing them in a sure proportion underneath a moderate heating. An elaboration of this upshot in DES formulation is shown, displaying that sugars like fructose, sucrose, glucose, and malic acid are solid at room temperature due to it has melting state over 130°C, at the same time as their combos (denoted as DESs) are in liquid shape [72]. On blending, the HBD and hydrogen bonds acceptor (HBA) constituents will intercommunicate with one another by hydrogen bonding. A naive example of DES synthesis made up of choline chloride and HBD via hydrogen bonding interactions is displayed. As proven, there’s a formation of hydrogen bonding interactions among the chloride ion of HBA with the OH groups of HBD [73].

11. Vegetable oils as green solvents

Vegetable oils, are oleochemicals that are pressed out from various plant sources and are renewable resources and have triglyceride shape. Vegetable oils are made from glycerol by the substitution of all hydroxyl groups of glycerol with various fatty acids which develop them into solid or liquid productions [74]. Vegetable oils are crucial meals constituent. Unluckily, they have now not been taken into consideration as a green solvent so far besides for some reactions such as the acylation reaction in corn oil [75]. Vegetable oils have been applied for biopolymers and are probably accepted by researchers who are seeking out brand new sources of green solvents. The cyclization and acylation reactions have occurred in vegetable oils, particularly corn oil. Applications and characteristic properties of vegetable oils have been discoursed and yields, time of reaction, and sustainability of vegetable oils have been equated with each other as well as with hazardous solvents such as xylene. A combination of dibenzoylmethane, phenol, and oxalyl chloride was heated in the presence of corn oil at 120°C for 15 minutes. Scientists have interpreted that CH2 of dibenzoylmethane turned into acylated very effortlessly. This reaction is the primary instance of vegetable oils and this concept must be focused on utilizing greater synthesis strategies because of the cost and effectiveness of vegetable oils [75].

12. Supercritical water and carbon dioxide as green solvents

The supercritical fluids, as the name suggest, are chemicals that reside in an intermediate phase across a substance that is liquid along with an air at pressures and temperatures over the corresponding critical points [60, 76]. The supercritical fluids may work such as gases or liquids and can be bypassed through solid substances or liquids like beverages, dissolving other substances. Furthermore, when each pressure and temperature are close to the critical level, converting them even marginally can bring about grievous density alterations.

Supercritical fluids are an aptest alternative to organic solvents for commercial and laboratory procedures. Generally, supercritical carbon dioxide (sCO2) or water is ordinarily expended supercritical fluid and is taken into consideration to greener solvent [60]. Owing to the extremely good dissolubility inside lots of polymer, supercritical carbon dioxide (sCO2) has an unreplaceable issue for polymers procedure. Moreover, the selection of less dangerous fluids like supercritical carbon dioxide (sCO2) in place of traditional organic solvents is a bonus to the surroundings [60, 77].

13. Applications of green solvents

ILs are utilized in the desulfurization technique to diminish SO2 eliminations in the petroleum enterprise [78]. The key industrious applications of green solvents have a huge variety from extraction processing to chemical synthesis such as sensors as well as biosensors, CO2 captured, lignocellulose biomass use, and bio-supported chemical substances [79]. Solvents utilized inside the pharmaceutic discipline reports for mass intake inside the variety of 80–90% and biosolvents for example butanol, glycol, polyethylene, bio-reusable materials along with supercritical fluids dissolvents have been extensively employed inside recovery and in the dissolution to drug [80]. The most aggressively addressed sustainable solvents during the aforementioned period were supercritical liquids, ILs along with deep eutectic fluids, predominantly used for the treatment of herbal remedies, foodstuffs, flavor, including perfume, in addition to the processor of medicine plants [81]. Organic carbonates are a category of organic compounds and reaction intermediates that are recognized for their eminent bio-degradation, low harmfulness, and versatility which cause their extensive applications in bio-catalysis [82]. Unconventional solvents are used for biomass pre-treatment as well as separation of natural polymeric materials from assets let in ILs, bio-based solvents, and DESs [83]. Another fascinating field is rare earth elements detail restoration and ionic solvents, which include ILs and deep-eutectic solvents, which are becoming a variety of hobby due to the fact they provide an alternate options to classical metallic healing techniques [84].

14. Green solvents in chemical reactions

With the developing advancements within the discipline of chemical studies, the capacity for danger to surroundings and human health has accelerated appreciably. Thus, to establish a chemist, extra surroundings-friendly magnificent interest has been paid to the characteristics and usages of green solvents in chemical processes, extractions and fractional processes, and synthesis of materials. Lots of procedures that exercise green solvents have been used for commercial purposes [85]. More a couple of examples of organic synthesis are addressed hereby utilizing green solvents as a replacement.

  1. Glycerol can work like a reducing agent in the presence of a metal catalyst in reactions, switch the hydrogenation of olefins, and might yield satisfactory outcomes and can be reused later on [85].

  2. In the Suzuki chemical reaction, the yield was nice among 4-iodotoluene and phenylboronic acid in PEG400 (90%) in comparison to other solvents including DMF and toluene.

  3. Ethylene glycol is a plentiful recyclable biomass, low-toxicity of solvent, that has prominent industrialized significance and is an outstanding green solvent for photo-catalyzed cascade cyclization processes [86].

15. Green solvents in environmental acceptable extraction techniques

Excellent belongings of ILs, potentiality to synthesize with specific dissolubility in water, and in organic mixtures like ethanenitrile or methanol causes their applications of extractions excitingly. Because of their viscosity, ILs have been applied in the chromatographic techniques as additives and after including high-performance liquid chromatography solutions, viscosity of ILs minimized [87, 88]. In unique extraction techniques capillary electrophoresis (CE), ILs are used as heritage electrolytes and additives. In Addition, ILs qualify the capillaries walls as well as electrophoresis separations [89, 90, 91]. ILs are also utilized inside the extraction of flavonoids compound from phenolic chemicals and imidazolium supported ILs, and ketoprofen, carprofen, naproxen, and suprofen by the ILs (C4mim) (NTf2). Researchers of natural products use applying of ILs as green solvents to isolate and extract from plants such as terpenoids, alkaloids, flavonoids, and phenolics compounds [92, 93, 94, 95].

Traditionally, investigators on the whole make use of unsafe unstable organic compounds (VOCs) in extraction techniques to have chemicals extracted like maceration soxhlet, distillations, percolations, and infusions. However, all chemists have long tried for substituting classical techniques that have an environment strike with green techniques such as microwave assisted extractions, supercritical fluids extractions, ultrasound-assisted separations, excessive-rate homogenizations, and pulsed electric field, and pressurized solvents. ILs scale back solvent uptake and extraction time. Supercritical fluids extraction has amazeballs extraction houses but a huge operating cost than ILs [96, 97, 98, 99, 100].

16. Green solvents as a catalyst for the preparation of bio-diesel

Worthless vapor pressure, excessive thermal constancy, state transformations conduct, dissolubility and mixability with chemicals, basic, and acidic, swappable ILs as green solvents, biodiesel production by ILs, catalyst, solvent for enzymes-catalyzed transesterifications, catalyst based, reusing for ILs, restoration of ILs, DESs which includes choline chlorides supported, the weird family for ILs seemed such a noble era for ILs which shape hydrogens bondings. In addition, hydrogens-bondings interplay in DES are high-energy advantageous as an outcome of greater dissolubility. Scientists have habituated a combining of ILs with deep eutectic solvents in biodiesel practise [101, 102].

17. Future approaches

Green chemistry has the potential to be leveraged to accomplish sustainability across three critical domains. Initially infinite inexhaustible energy resources, whereby scientists foster the financially feasible process for converting the sun’s energy towards chemically generated energy. Secondly, petrochemicals are the biggest supplier of the chemicals utilized throughout the manufacturing industries, along with more and more need to be sourced from renewable resources to subdue our habituation of fossil carbon. Thirdly, technologies that might be harmful to the surroundings need to get replaced by way of nontoxic alterations.

The biannual environmentally conscious solvents convention, which continues to conduct events during the time 2002, has grown into a crucial venue for conversation to breakthroughs in science including business application by using ameliorated solvents enabling reactions processes as well as approaches. These multidisciplinary assembly dealt the exploitation with applications of the optional solvents, admitting aqueous stage to inappropriate applications, ILs and supercritical liquids, in addition to green natural solvents and soluble polymers. Other subjects have been admitted protected without solvents procedures, and substances treating solutions, phases extractable chemicals, with numerous abstraction techniques [103]. This extraction performance and compounds structures fit nicely to industries functions.

Followings include some alternates for common solvents:

  • 2-MeTHF as well as CPME both are created by furfural, that are the biology-based compounds. These are extremely helpful to substitute dangerous chemical compounds inclusive of THF. 2MeTHF an outstanding benefits for demanding natural biological cycles. Solvents close off circle are much critical for making sure, not again harm for surroundings takes place. These are splendid opportunities to have a look at the applicability of 2MeTHF within the chemical processing industries [104].

  • Propylene carbonate (PC) is also an essential green solvent with a purpose to eat CO2 that is provided. Several biological operations can develop this CO2, such as bio-ethanol. PC has been also discovered as a desirable replacement to THF.

  • The beauty sector has made 1,3-propanediol a crucial solvent, and it can be applied to an extensive variety of applications along with ketonic group inside chemical solvents. Additionally, it can be deployed in the creation of recyclable polymers [105].

  • DCM solvent has been upgraded with ethyl lactate. Additionally, it has applications of excellent potency to eliminate caffeine of tea [106].

18. Conclusions

Our forthcoming natural world sustainability challenges demand an effective alternatives, and green technologies for paving the manner for such an approaches. Glycerol, ILs, water can be taken into consideration as the naive green solvents as well as their overall functioning and top production, these include the most frequently employed commercial noble glowing solvents of choice, as demonstrated by outcomes. Additionally other solvents, such as 2-MeTHF, CPME, and ethyl lactate, have been verified as more environmentally friendly alternatives to standard solvents in terms of inhibiting and avoiding contamination. Twelve ideas of sustainable chemistry shape an idea of developing greener solvents inside gases phase, liquids phase, and solid phase with appropriate efficiency. According to European solvent industrial enterprise, the complete ban of VOCs will damage the industry but their proper and acceptable management is essential to scale down the solvent-supported whole environment depletion.

Acknowledgments

I owe my profoundest admiration to my supervisor, Assoc. Prof. Deepali Jain of D.N. College, Meerut for unforgettable affirms, directions, advancement, and freedom to investigate novel viewpoints in my field of study. She, the inspiration behind these paintings, created a partner for me in the realm of green chemistry and green solvents.

She supported me through all of the issues we encountered while serving as my supervisor, allowing me to take on new tasks. I want to express my gratitude to the entire faculty of the chemistry department at N.A.S. college, CCS University, Meerut, as well as to all of my colleagues for their support and for providing me with tonnes of inspiration and ideas.

Competing interests

The authors say they have no competing interests.

References

  1. 1. Anastas P, Eghbali N. Green chemistry: principles and practice. Chemical Society Reviews. 2009;39(1):301-312. DOI: 10.1039/b918763b
  2. 2. Anastas PT, Williamson TC. Green Chemistry: Designing Chemistry for the Environment. Washington, DC: American Chemical Society, ACS Symposium Series No 626; 1996
  3. 3. Collins TJ. Green chemistry. In: Lagowsky JJ editor. Macmillan Encyclopedia of Chemistry Simon and Schuster. Vol. 2. New York: Macmillan; 1997. pp. 691-697
  4. 4. Welton T. Solvents and sustainable chemistry. Proceedings of the Royal Society. 2015;471(A):20150502
  5. 5. Jutz F, Adanson JM, Balker A. Ionic liquids and dense carbon dioxide: a beneficial biphasic system for catalysis. Chemical Reviews. 2011;111(2):322-353
  6. 6. Sanni Babu N, Mutta Reddy S. Impact of solvents leading to environmental pollution. National Seminar on Impact of Toxic Metals, Minerals and Solvents leading to Environmental Pollution. Journal of Chemical and Pharmaceutical Sciences. 2014. ISSN: 0974-2115 (Special Issue 3: October 2014)
  7. 7. Dick FD. Solvent neurotoxicity. Occupational and Environmental Medicine. 2006;63(3):221-226
  8. 8. Malaguarnera G, Cataudella E, Giordano M, Nunnari G, Chisari G, Malaguarnera M. Toxic hepatitis in occupational exposure to solvents. World Journal of Gastroenterology. 2012;18(22):2756-2766
  9. 9. Lauwerys R, Bernard A, Viau C, Buchet JP. Kidney disorders and hematotoxicity from organic solvent exposure. Scandinavian Journal of Work, Environment & Health. 1985;11(1):83-90
  10. 10. Rama Koteswararao P, Tulasi SL, Pavani Y. Impact of solvents on environmentl pollution. National Seminar on Impact of Toxic Metals, Minerals and Solvents leading to Environmental Pollution. Journal of Chemical and Pharmaceutical Sciences. 2014. ISSN: 0974-2115 (Special Issue 3: October 2014)
  11. 11. Available from: https://www.cdc.gov/niosh/topics/emres/chemagent.html [Last accessed: 02 Oct 2021]
  12. 12. Available from: https://www.canada.ca/en/health-canada/services/health-effects-chemical-exposure.html [Last accessed: 30 Sep 2021]
  13. 13. Available from: https://www.esig.org/regulatory/air-quality [Last accessed: 25 Sep 2021]
  14. 14. Available from: https://www.environmentalpollutioncenters.org/organic-solvents [Last accessed: 25 Sep 2021]
  15. 15. Available from: https://www.solvents.org.uk/solvents-and-the-environment [Last accessed: 02 Oct 2021]
  16. 16. Capello C, Fischer U, Hungerbuhler K. What is a green solvent? A comprehensive framework for the environmental assessment of solvents. Green Chemistry. 2007;9:927-934
  17. 17. Capello C, Wernet G, Sutter J, Hellweg S, Hungerbuhler K. A comprehensive environmental assessment of petrochemical solvent production. International Journal of Life Cycle Assessment. 2009;14:467-479
  18. 18. Available from: https://www.statista.com/statistics/407861/forecast-for-annual-growth-in-chemical-industry-worldwide-by-region [Last accessed: 23 Sep 2021]
  19. 19. Agata T. Green solvents. Journal of Education, Health and Sport. 2017;7(9):224-232
  20. 20. Menges N. The role of green solvents and catalysts at the future of drug design and of synthesis. In: Saleh HEDM, Koller M, editors. Green Chemistry. Boston, USA: IntechOpen; 2017. pp. 74-89. Ch. 5
  21. 21. Simon MO, Li CJ. Green chemistry oriented organic synthesis in water. Chemical Society Reviews. 2012;41(4):1415-1427
  22. 22. Greer AJ, Jacquemin J, Hardacre C. Industrial Applications of Ionic Liquids. Basel Switzerland: Multidisciplinary Digital Publishing Institute; 2020. pp. 1-2
  23. 23. Tanzi CD, Vian MA, Ginies C, Elmaataoui M, Chemat F. Terpenes as green solvents for extraction of oil from microalgae. Molecules Journal. 2012;17(7):8196-8205
  24. 24. Breslow R. The principles of and reasons for using water as a solvent for green chemistry, part 5 reactions in water. In: Li CJ editor. Handbook of Green Chemistry. Germany: Wiley-VCH Verlag GmbH & Co. KGaA; 2015. pp. 1-3
  25. 25. Wanga XL, Lub Y, Shib L, Yanga D, Yanga Y. Novel low viscous hydrophobic deep eutectic solvents liquid-liquid microextraction combined with acid base induction for the determination of phthalate esters in the packed milk samples. Microchemical Journal. 2020;159:105332
  26. 26. Moura L, Moufawad T, Ferreira M, Bricout H, Tilloy S, Monflier E, et al. Deep eutectic solvents as green absorbents of volatile organic pollutants. Environmental Chemistry Letters. 2017;1:2-5
  27. 27. Abro R, Abdeltawab AA, Al-Deyab SS, Yu G, Qazi AB, Gaoa S, et al. A review of extractive desulfurization of fuel oils using ionic liquids. Royal Society of Chemicals. 2014;67:5-6
  28. 28. Shukla SK, Khokarale SG, Bui TQ , Mikkola JT. Ionic liquids: potential materials for carbon dioxide capture and utilizations. Frontiers in Materials. 2018;6:42
  29. 29. Rapinel V, Rombaut N, Rakotomanomana N, Vallageas A, Cravotto G, Chemat F. An original approach for lipophilic natural products extraction: use of liquefied nbutane as alternative solvent to n-hexane. LWT-Food Science and Technology. 2016;85:524-533
  30. 30. Kemmere MF, Meyer T. Super critical carbon dioxide. In: Meyer T editor. Polymer Reaction Engineering. Germany: Wiley-VCH Verlag GmbH & Co. KGaA; 2005. pp. 3-8. Ch. 5
  31. 31. Escobar ELN, da Silva TA, Pirich CL, Corazza ML, Ramos LP. Supercritical fluids: a promising technique for biomass pretreatment and fractionation. Frontiers in Bioenjineering and Biotenchnology. 2020;8:252
  32. 32. Diacon A, Calinescu I, Vinatoru M, Chipurici P, Vlaicu A, Boscornea AC, et al. Fatty acid ethyl esters (FAEE): a new, green and renewable solvent for the extraction of carotenoids from tomato waste products. Molecules. 2021;26:4388
  33. 33. Available from: https://www.merckmillipore.com/IN/en/reagents-chemicals-and labware/bioethanol/86Kb.qB.LIk AAAFDdo9xDMUX,nav?ReferrerURL=https%3A%2F%2 Fwww.google.com%2F [Last accessed: 27 Sep 2021]
  34. 34. Mensah MB, Awudza JAM, ‘O’Brien P. Castor oil: a suitable green source of capping agent for nanoparticle syntheses and facile surface functionalization. Royal Society Open Science. 2018;5:180824
  35. 35. Mubofu EB. Castor oil as a potential renewable resource for the production of functional materials. Sustainable Chemical Processes. 2016;4:11
  36. 36. Villanueva-Bermejo D, Reglero G, Fornari T. Recent advances in the processing of green tea biomolecules using ethyl lactate a review. Trends in Food Science and Technology. 2017;62:1-12
  37. 37. Paul S, Pradhan K, Das AR. Ethyl lactate as a green solvent: a promising bio-compatible media for organic synthesis. Current Green Chemistry. 2016;3(1):112-117
  38. 38. Vafaeezadeh M, Hashemi MM. Polyethylene glycol (PEG) as a green solvent for carbon-carbon bond formation reactions. Journal of Molecular Liquids. 2015;207:73-79
  39. 39. Pont AL, Marcilla R, De Meatza I, Grande H, Mecerreyes D. Pyrrolidinium- based polymeric ionic liquids as mechanically and electrochemically stable polymer electrolytes. Journal of Power Sources. 2009;188(2):558-563
  40. 40. Freire MG, Neves CM, Marrucho IM, Coutinho JA, Fernandes AM. Hydrolysis of tetrafluoroborate and hexafluorophosphate counter ions in imidazolium-based ionic liquids. The Journal of Physical Chemistry A. 2009;114(11):3744-3749
  41. 41. Kogelnig D, Stojanovic A, Galanski M, Groessl M, Jirsa F, Krachler R, et al. Greener synthesis of new ammonium ionic liquids and their potential as extracting agents. Tetrahedron Letters. 2008;49(17):2782-2785
  42. 42. Gao H, Luo M, Xing J, Wu Y, Li Y, Li W, et al. Desulfurization of fuel by extraction with pyridinium-based ionic liquids. Industrial & Engineering Chemistry Research. 2008;47(21):8384-8388. DOI: 10.1021/ie800739w
  43. 43. Breitbach ZS, Armstrong DW. Characterization of phosphonium ionic liquids through a linear solvation energy relationship and their use as GLC stationary phases. Analytical and Bioanalytical Chemistry. 2008;390(6):1605-1617
  44. 44. Paduszyński K, Domańska U. Experimental and theoretical study on infinite dilution activity coefficients of various solutes in piperidinium ionic liquids. The Journal of Chemical Thermodynamics. 2013;60:169-178
  45. 45. Earle MJ, Esperança JM, Gilea MA, Lopes JNC, Rebelo LP, Magee JW, et al. The distillation and volatility of ionic liquids. Nature. 2006;439(7078):831-834
  46. 46. Ye C, Liu W, Chen Y, Yu L. Room-temperature ionic liquids: a novel versatile lubricant. Chemical Communications. 2001;21:2244-2245
  47. 47. Seddon KR. Ionic liquids for clean technology. Journal of Chemical Technology and Biotechnology. 1997;68(4):351-356
  48. 48. He Z, Alexandridis P. Nanoparticles in ionic liquids: Interactions and organization. Physical Chemistry Chemical Physics. 2015;17(28):18238-18261
  49. 49. Noda A, Hayamizu K, Watanabe M. Pulsed-gradient spin-echo 1H and 19F NMR ionic diffusion coefficient, viscosity, and ionic conductivity of non-chloroaluminate room temperature ionic liquids. The Journal of Physical Chemistry B. 2001;105(20):4603-4610
  50. 50. Welton T. Room-temperature ionic liquids. Solvents for synthesis and catalysis. Chemical Reviews. 1999;99:2071
  51. 51. Shariati A, Gutkowski K, Peters CJ. Comparison of the phase behavior of some selected binary systems with ionic liquids. AIChE Journal. 2005;51:1532
  52. 52. Brennecke JF, Maginn EJ. Ionic liquids: Innovative fluids for chemical processing. AIChE Journal. 2001;47:2384
  53. 53. Varma R. Solvent-free organic syntheses. Using supported reagents and microwave irradiation. Green Chemistry. 1999;1(1):43-55
  54. 54. Davoodnia A, Heravi MM, Safavi-Rad Z, Tavakoli-Hoseini N. Green, one-pot, solvent free synthesis of 1, 2, 4, 5-tetrasubstituted imidazoles using a Brønsted acidic ionic liquid as novel and reusable catalyst. Synthetic Communications. 2010;40(17):2588-2597
  55. 55. Endres F, ElAbedin SZ. Air and water stable ionic liquids in physical chemistry. Physical Chemistry Chemical Physics. 2006;8(18):2101-2116
  56. 56. Bonhote P, Dias A-P, Papageorgiou N, Kalyanasundaram K, Grätzel M. Hydrophobic, highly conductive ambient-temperature molten salts. Inorganic Chemistry. 1996;35(5):1168-1178
  57. 57. Dupont J. From molten salts to ionic liquids: a “nano” journey. Accounts of Chemical Research. 2011;44(11):1223-1231
  58. 58. Hough-Troutman WL, Smiglak M, Griffin S, Reichert WM, Mirska I, Jodynis-Liebert J, et al. Ionic liquids with dual biological function: sweet and antimicrobial, hydrophobic quaternary ammonium-based salts. New Journal of Chemistry. 2009;33(1):26-33
  59. 59. Narayan S, Muldoon J, Finn MG, Fokin VV, Kolb HC, Sharpless KB. “On Water”: unique reactivity of organic compounds in aqueous suspension. Angewandte Chemie International Edition. 2005;44:3275-3279
  60. 60. Sharma SR. Green chemistry, green solvents and alternative techniques in organic synthesis. International Journal of Chemical and Physical Sciences. 2015;4:516-520. (Special Issue-NCSC-Jan-2015)
  61. 61. Breslow R. The principles of and reasons for using water as a solvent for green chemistry. In: Part 5. Reactions in Water Published Online. Germany: Wiley-VCH Verlag GmbH & Co. KGaA; 2010
  62. 62. Chanda A, Fokin VV. Oragnic synthesis “on water”. Chemical Reviews. 2009;109(2):725-748
  63. 63. Narayan S, Fokin V, Sharpless K. Organic reactions in water. In: Lindstrom M editor. Principles, Strategies and Applications. Oxford: Blackwell; 2007. pp. 350-365
  64. 64. Breslow R, Maitra U. On the origin of product selectivity in aqueous diels-alder reactions. Tetrahedron Letters. 1984;25:1239-1240
  65. 65. Abbott AP, Capper G, Davies DL, Rasheed RK, Tambyrajah V. Novel solvent properties of choline chloride/urea mixtures. Chemical Communications. 2003;39:70-71
  66. 66. Guthrie F. LII. On eutexia. The London, Edinburgh, and Dublin Philosophical Magazine and Journal of Science. 1884;17:462-482
  67. 67. Martins MA, Pinho SP, Coutinho JAP. Insights into the nature of eutectic and deep eutectic mixtures. Journal of Solution Chemistry. 2019;48:962-982
  68. 68. Perna FM, Vitale P, Capriati V. Deep eutectic solvents and their applications as green solvents. Current Opinion in Green and Sustainable Chemistry. 2020;21:27-33
  69. 69. Florindo C, Lima F, Ribeiro BD, Marrucho IM. Deep eutectic solvents: overcoming 21st century challenges. Current Opinion in Green and Sustainable Chemistry. 2019;18:31-36
  70. 70. Paiva A, Matias AA, Duarte ARC. How do we drive deep eutectic systems towards an industrial reality? Current Opinion in Green and Sustainable Chemistry. 2018;11:81-85
  71. 71. Smith EL, Abbott AP, Ryder KS. Deep eutectic solvents (DESs) and their applications. Chemical Reviews. 2014;114:11060-11082
  72. 72. Choi YH, van Spronsen J, Dai Y, Verberne M, Hollmann F, Arends IW, et al. Are natural deep eutectic solvents the missing link in understanding cellular metabolism and physiology? Plant Physiology. 2011;156:1701-1705
  73. 73. Santos LB, Assis RS, Barreto JA, Bezerra MA, Novaes CG, Lemos VA. Deep eutectic solvents in liquid-phase microextraction: contribution to green chemistry. TrAC Trends in Analytical Chemistry. 2021;146:116478
  74. 74. O’Brien RD. Fats and Oils: Formulating and Processing for Applications. 3rd ed. Boca Raton, USA: CRC Press; 2005
  75. 75. Menges N, Şhin E. Metal- and base-free combinatorial reaction for C-acylation of 1,3-diketocompounds in vegetable oil: The effect of natural oil. ACS Sustainable Chemistry & Engineering. 2014;2:226-230
  76. 76. Branch JA, Bartlett PN. Electrochemistry in supercritical fluid. Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences. 2015;373(2057):20150007
  77. 77. Nalawade SP, Picchioni F, Janssen LPBM. Supercritical carbon dioxide as a green solvent for processing polymer melts: processing aspects and applications. Progress in Polymer Science. 2006;31(1):19-43
  78. 78. Dharaskar SA. The green solvents for petroleum and hydrocarbon industries. Research Journal of Chemical Sciences. 2012;2(8):80-84
  79. 79. Mallakpour S, Rafiee Z. Fundamental and industrial application. In: Inamuddin MA editor. Green Solvents. Millersville, PA, USA: Springer; 2012. pp. 10-50. Ch. 1
  80. 80. Hussain EA. Green solvents for drug synthesis, green sustainable process for chemical and environmental engineering and science. In: Inamuddin R, Boddula MI, Ahamed AM, Asiri AM, editors. Solvents for the Pharmaceutical Industry. Amsterdam, Netherlands: Elsevier; 2021. pp. 55-86. Ch. 4
  81. 81. Choi YH, Verpoorte R. Green solvents for the extraction of bioactive compounds from natural products using ionic liquids and deep eutectic solvents. Current Opinion in Food Science. 2019;26:87-93
  82. 82. Truong CC, Mishra DK, Mishra V. Organic carbonate as a green solvent for biocatalysis. In: Inamuddin, Boddula R, Ahamed MI, Asiri AM, editors. Green Sustainable Process for Chemical and Environmental Engineering and Science. Amsterdam, Netherlands: Elsevier; 2021. pp. 253-270. Ch. 13
  83. 83. Prasad K, Sharma M. Green solvents for the dissolution and processing of biopolymers. Current Opinion in Green and Sustainable Chemistry. 2019;18:72-78
  84. 84. Arrachart G, Couturier J, Dourdain S, Levard C, Pellet-Rostaing S. Recovery of Rare Earth Elements (REEs) Using Ionic Solvents. Multidisciplinary Digital Publishing Institute. 2021;9:1202
  85. 85. Díaz-Álvarez AE, Cadierno V. Glycerol: a promising green solvent and reducing agent for metal-catalyzed transfer hydrogenation reactions and nanoparticles formation. Applied Sciences. 2013;3(1):55-69
  86. 86. Jiang Y, Li J, Feng ZW, Xu G, Shi X, Ding QJ, et al. Ethylene glycol: a green solvent for visible light-promoted aerobic transition metal-free cascade sulfonation/cyclization reaction. Advanced Synthesis and Catalysis. 2020;362(13):2609-2614
  87. 87. Berthod A, Carda-Broch S. A new class of solvents for CCC: the room temperature ionic liquids. Journal of Liquid Chromatography and Related Technologies. 2003;26:1493-1508
  88. 88. Marszall MP, Kaliszan R. Application of ionic liquids in liquid chromatography. Critical Reviews in Analytical Chemistry. 2007;37:127-140
  89. 89. Merike V, Mihkel K, Mihkel K. Ionic liquids as electrolytes for nonaqueous capillary electrophoresis. Electrophoresis. 2002;23:426-430
  90. 90. Yanes EG, Gratz SR, Baldwin MJ, Robison SE, Stalcup AM. Capillary electrophoretic application of 1-alkyl-3-methylimidazolium-based ionic liquids. Analytical Chemistry. 2001;73:3838-3844
  91. 91. López-Pastor M, Simonet BM, Lendl B, Valcárcel M. Ionic liquids and CE combination. Electrophoresis. 2008;29:94-107
  92. 92. Yue ME, Shi YP. Application of 1-alkyl-3-methylimidazolium-based ionic liquids in separation of bioactive flavonoids by capillary zone electrophoresis. Journal of Separation Science. 2006;29:272-276
  93. 93. François y, Varenne A, Juillerat E, Servais AC, Chiap P, Gareil P. Nonaqueous capillary electrophoretic behavior of 2-aryl propionic acids in the presence of an achiral ionic liquid a chemometric approach. Journal of Chromatography. A. 2007;1138:268-275
  94. 94. Ventura SP, Fa ES, Quental MV, Mondal D, Freire MG, Coutinho JA. Ionic-liquid mediated extraction and separation processes for bioactive compounds: past, present, and future trends. Chemical Reviews. 2017;117:6984. DOI: 10.1021/acs.chemrev.6b00550
  95. 95. Zhao CN, Zhang JJ, Li Y, Meng X, Li HB. Microwave- assisted extraction of phenolic compounds from Melastoma sanguineum fruit: optimization and identification. Molecules. 2018;23:2498. DOI: 10.3390/molecules2310249
  96. 96. Chemat F, Vian MA, Cravotto G. Green extraction of natural products: conceptand principles. International Journal of Molecular Sciences. 2012;13:8615. DOI: 10.3390/ijms13078615
  97. 97. Ibañez E, Cifuentes A. Green Extraction Techniques: Principles, Advances and Applications. Amsterdam: Elsevier; 2017
  98. 98. Soquetta MB, Terra LM, Bastos CP. Green technologies for the extraction of bioactive compounds in fruits and vegetables. CyTA – Journal of Food. 2018;16:400. DOI: 10.1080/19476337.2017.1411978
  99. 99. Chemat F, Vian MA. Alternative Solvents for Natural Products Extraction, Green Chemistry and Sustainable Technology. Berlin, Heidelberg: Springer Verlag; 2014. DOI: 10.1007/978-3-662-43628-8
  100. 100. Torres-Valenzuela LS, Ballesteros-Gomez A, Rubio S. Green solvents for the extraction of high added-value compounds from agri-food waste. Food Engineering Reviews. 2020;12:83. DOI: 10.1007/s12393-019-09206-y
  101. 101. Nkuku CA, LeSuer RJ. Journal of Physical Chemistry. 2007;11:13271
  102. 102. Zhao H, Baker GA. Journal of Chemical Technology & Biotechnology. 2013;88:3
  103. 103. Available from: https://axial.acs.org/2018/04/02/green-solvents-embrace-future [Last accessed: 25 Sep 2021]
  104. 104. Pace V, Hoyos P, Castoldi P, de Mara D, Alcntara AR. 2-methyltetrahydrofuran (2-MeTHF): a biomass-derived solvent with broad application in organic chemistry. ChemSusChem. 2012;5(8):1369-1377
  105. 105. Forero JSB, Muñoz JH, Jones J, da Silva JFM. Propylene carbonate in organic synthesis: exploring its potential as a green solvent. Current Organic Synthesis. 2016;13:834-844
  106. 106. Bermejo DV, Mendiola JA, Ibánez E, Reglero G, Fornari T. Pressurized liquid extraction of caffeine and catechins from green tea leaves using ethyl lactate, water and ethyl lactate +water mixtures. Food and Bioproducts Processing. 2015;96:106-111

Written By

Parul Tomar and Deepali Jain

Submitted: 20 July 2023 Reviewed: 27 July 2023 Published: 25 August 2023