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1 This article gives overview of the lignin separation methods from lignocellulosic biomass using various methods but the main attention has been paid on lignin separation using ionic liquids
Merlin Raud
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Hasanov, I.; Raud, M.; Kikas, T. Ionic Liquids and Lignin. Encyclopedia. Available online: https://encyclopedia.pub/entry/2389 (accessed on 16 November 2024).
Hasanov I, Raud M, Kikas T. Ionic Liquids and Lignin. Encyclopedia. Available at: https://encyclopedia.pub/entry/2389. Accessed November 16, 2024.
Hasanov, Isa, Merlin Raud, Timo Kikas. "Ionic Liquids and Lignin" Encyclopedia, https://encyclopedia.pub/entry/2389 (accessed November 16, 2024).
Hasanov, I., Raud, M., & Kikas, T. (2020, October 07). Ionic Liquids and Lignin. In Encyclopedia. https://encyclopedia.pub/entry/2389
Hasanov, Isa, et al. "Ionic Liquids and Lignin." Encyclopedia. Web. 07 October, 2020.
Ionic Liquids and Lignin
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This entry is adapted from the peer-reviewed paper 10.3390/en13184864

This entry gives overview of the lignin separation methods from lignocellulosic biomass using various methods but the main attention has been paid on lignin separation using ionic liquids. Lignin is a natural polymer, one that has an abundant and renewable resource in biomass. Due to a tendency towards the use of biochemicals, the efficient utilization of lignin has gained wide attention. The delignification of lignocellulosic biomass makes its fractions (cellulose, hemicellulose, and lignin) susceptible to easier transformation to many different commodities like energy, chemicals, and materials that could be produced using the biorefinery concept. 

Lignocellulosic biomass lignin ionic liquids

1. Introduction

Lignocellulosic (LC) biomass is the most abundant plant material for the production and sustainable supply of liquid biofuels at a relatively low cost [1]. It mainly consists of sugar polymers (cellulose and hemicellulose) and lignin [2]. These three biopolymers, depicted in Figure 1, are the main constituents of plant cell walls [3]. The lignin and hemicelluloses forms a cross-linked matrix which covers the cellulose fibers and thereby forms a tight and, compact structure [4]. Lignin is one of the three primary components of LC biomass which, protects cellulose and hemicellulose by providing mechanical strength but also hydrophobic and indigestible properties to plant cell walls [5][6].

Energies 13 04864 g001 550

Figure 1. Structure of lignocellulosic biomass (Modified from [7][8]).

However, the large volumes of lignin resources never been cost efficiently used [6]. It is clear that the chemical pulp industries globally produce about 50 million tons of lignin every year [9]. Despite that, the commercially utilized lignin is only about 2% of total, while the rest is used for combustion in order to produce heat and energy [10]. The use of cheap and renewable bioresources, like lignin, has been attractive since the increasing depletion of fossil fuel resources is concerning level [10]. Besides of economic value, the use of renewable bioresources has potential to decrease the negative effects of the production and use of fuels and chemicals on environment and health [10]. Lignin is the only natural biopolymer containing aromatic phenolpropanoid monomers. Therefore, it can be utilized to produce value-added end products, for example fuel components, via a process of depolymerization [11].

An efficient low-cost technique is required to remove and recover the lignin from biomass to gain enable easier access to the biomass polysaccharides in order to produce different products from lignin [12]. Due to the complexed structure of cell wall microfibrils in LC biomass, the immaculate separation of celluloses and lignin resulting minimal degradation of polymers is a great challenge [11]. Among the various reported biomass pretreatment technologies, pretreatment with ionic liquids (ILs) has shown the most feasible results, especially in a sense of lignin separation [11]. The properties such as no measurable vapor pressure, wide electrochemical window, high thermal stability, nonflammability, excellent solvent power for both organic and inorganic substances, etc.—makes ILs unique and versatile among its kind [13]. More importantly, the ILs properties where they relate to hydrophobicity, polarity, and solvent power can be modified by combining or modifying the cations and anions [14].

2. LC Pretreatment for Lignin Isolation

Lignin separation from the LC biomass is carried out by applying various pretreatment processes [15][16]. As a result of complicated structure and molecular interactions with other components like hemicellulose, dissolution of the natural lignin in wood is very complicated and money consuming procedure. The required methods to separate lignin from the plant cell walls and cellulose, are quite harsh and this partially changes its native conformation [17].

Technical lignins are lignins which are separated from various biomasses during one of a number of available technical processes [18]. Among these are kraft lignin, soda lignin, organosolv lignin, ionic liquid lignin, and hydrolysis lignin. On the other hand, native lignin is lignin in its original form present in LC biomasses, which are, wood lignin (MWL), cellulolytic enzymatic lignin (CEL), and enzymatic mild acidolysis lignin (EMAL).

MWL is mostly used as standard lignin because of its closeness to the native lignin structure. Chang et al. reported the CEL treatment procedure, to further reduction for the isolation-induced modifications [19]. Contrary to MWL, the CEL was obtained in higher yields, in the same milling duration, therefore, it was less degraded. Due to that, CEL is considered more similar to the total lignin fraction in wood. Enzymatic mild acidolysis lignin (EMAL) extraction was studied by Guerra et al. which is more complex procedure that combines milling, enzymatic treatment, and an additional acidolysis step [20]. The aim of the study was the further maximize the yield of the isolated lignin. Moreover, to the researches focused on simplifying the methods for lignin isolation in order to make them more environmentally clean, as well as to obtain lignin closer to its native structure [21].

Usually, Kraft lignin, alkaline, or organosolv lignin are used to test the dissolution rate of lignin. The choices are made considering their commercial availability, that they are products of the chemical pulping process [22]. Kraft lignin refers to the use of the alkaline degradation of LC, while sulfonated lignin arises from the use of a sulfite pulping process. In addition, the pulp and paper industries, extract Kraft lignin from black liquor.

Hydrolysis lignin (HL) is a by-product of enzymatic hydrolysis and fermentation processes in cellulosic ethanol plants. It is primarily consist of lignin (up to 60%) balanced with unreacted cellulose and mono- and oligosaccharides. Further modifications are required for the utilization of HL which are too expensive at the moment otherwise the HL-derived materials do not function well. As a result of this, the majority of HL is disposed without any valorization [23].

The structure of isolated lignin, cellulose, and hemicellulose depends upon the pretreatment method being used. For the separation of lignin from the LC biomass the used methods should focus on; increasing of the accessibility surface area, and cellulose decrystallization, partial depolymerization of cellulose and hemicellulose, maximizing the enzymatic digestibility of the pretreated material, minimizing the sugar-losses, and minimizing capital plus operating costs [24].

The used lignin extraction methods affect the dissolution behavior of lignin. For example, lignosulphonate, Kraft, and soda lignin are soluble in aqueous solvent, while alkali and organosolv lignins are soluble in a wide range of organic solvents [25].

For obtaining the separation of lignin from LC biomasses, there are four broad categories of pretreatment processes, which are; physical pretreatment, chemical pretreatment, physiochemical pretreatment, and native lignin separation (Figure 2).

Energies 13 04864 g003 550

Figure 2. Classification of different lignin separation methods.

Lignin Separation with ILs

Several studies have presented that different solvents like ethylene glycol, DMSO [26], ILs [27], g-valerolactone [28] and Tween-80/H2O are able to dissolve up to 70 wt% lignin [29]. Among these solvents, ILs have acquired especial levels of interest due to their particular chemo-physical properties when compared to traditional molecular solvents.

ILs are molten salts which are also named as being room temperature salts because they are in a liquid state at, or close to liquid state, ambient conditions [30]. The IL-s dissolve a wide range of materials including hydrophobic, hydrophilic, and polymeric compounds [31]. The ability of ILs to be an effective form of disruption targeting the non-covalent interactions between these polymers [32].

In essence, the ILs are formed by a combination of organic cations with organic or inorganic anions, and the desired properties of IL were precursor on the choice of ions [33]. Ion pairs are the parts of all ILs, and the possible combinations of cations and anions are endless. Generally, lignin solubility is high for five groups of ILs containing imidazolium, pyridinium, pyrrolidinium, ammonium, and phosphonium cations. The anions of IL usually include BF4−, FAP−, Tf2N−, OTF−, Cl−, PF6−, CH3COO−, and N(CN)2−. Large non-coordinating anions, such as [BF4]− and [PF6]−, showed low lignin dissolution ability [34].

ILs attract attentions due to their appealing properties. These properties include a wide electrochemical range, low vapor pressure, high thermal stability, and outstanding ionic conductivity even under anhydrous conditions. The dissolution properties of ILs are unique and can be tuned by choosing suitable cations and/or anions. One of the most desirable advantages of ILs in comparison with traditional molecular solvents is its extremely low vapor pressure [35].

Recent studies report that certain ILs have turned up to be very effective in terms of LC biomass delignification. Due to this, they have been considered as fractionation solvents for LC materials. ILs intensify the access to lignin by dissolving LC biomass, which in response leads to the possible further valorization of lignin. Different strategies can be applied during or after IL-aided fractionation in order to produce fuels, chemicals, and materials. These include the extraction of lignin from lignocelluloses, catalytic delignification to acquire separated lignin components from biomass, and the saccharification of polysaccharides that are attached to lignin fragments [28]. Delignification causes disruption of lignin structure, resulting in biomass swelling, which is not feasible in a sense of native lignin.

Hydrogen bond acceptability in IL anions is necessary for efficient biomass dissolution because it contributes to the formation of the hydrogen bonds with biomass components. Considering that, cations should contain strong acidic protons and short side chains to attain the reduction of the inhibition between the IL and biomass during dissolution [36]. As an exception, Muhammad et al. presented their findings which stated that the [Ch][PrOO] IL has a poor dissolution ability, despite of a high hydrogen basicity [32]. This behavior was explained by the internal interaction between the hydroxyl end group of IL cation and its anion.

The dissolution of lignin has been investigated in several aprotic and protic ILs (PILs) (see Table 1). The ILs with moderate hydrogen-bonding anions represents better ability to dissolve lignin [37].

Table 1. The dissolution of lignin with ionic liquids (ILs) and protic ionic liquids (PILs).

Sample Solvent Temp (°C) Time (h) Lignin (%) Cellulose (%) References
Kraft lignin Py 90 24 >50 0.10 ± 0.00 [38]
Kraft lignin Mim 90 24 >50 0.24 ± 0.02 [38]
Kraft lignin Pyrr 90 24 7.98 ± 0.10 0.63 ± 0.00 [38]
Kraft lignin HAc 90 24 0.72 ± 0.04 0.07 ± 0.01 [38]
Kraft lignin [Py] [For] 75 1 70 <1 [39]
Kraft lignin [Py] [Pro] 75 1 55   [40]
Kraft lignin [Py] [Ac] 75 1 64   [41]
Kraft lignin [Mmim] [MeSO4] 80 24 50   [41]
Kraft lignin [Bmim] [CF3SO3] 80 24 50   [38]
Kraft lignin [Py] [Ac] 90 24 >50 0.12 ± 0.03 [38]
Kraft lignin [Mim] [Ac] 90 24 >50 0.20 ± 0.05 [38]
Kraft lignin [Pyrr] [Ac] 90 24 >50 0.79 ± 0.04 [42]
Kraft lignin GVL/[Bmim]Ac 30   20.9   [42]
Kraft lignin GVL/[Bmim]Ac 60   28.0   [42]
Kraft lignin GVL/[Amim]Cl 30   13.4   [42]
Kraft lignin GVL/[Amim]Cl 60   43   [43]
Kraft lignin [Emim]Ac/water 60   38   [21]
Pinus radiata [C2mim] Ace 100 2 58   [21]
Pinus radiata [C4mim] Ace 100 2 63   [21]
Pinus radiata [C4mim]Ace/DMSO 100 2 51   [44]
Maple [Emim]Ac 110 1.5 9   [44]
Maple [Emim]Ac 130 24 6   [44]
Maple [Mmim] [MeSO4] 80 24 43.4a   [44]
Maple [Bmim] [CF3SO3] 80 24 5.8b   [40]
Birch [Emim] [OAc] 110 16 97c   [45]
Polar wood [Emim] [OAc] 110 16 85.3c   [46]
Bagasse [Emim] [ABS] 190 1–1.5 60.0c   [47]
Bamboo [Emim] [Gly] 120 8 13.7a   [28]
Corn stover [Emim] [OAc]/NMP 140 1 10.51a   [28]
Cotton stalk [Amim] [Cl]/DMSO 130 4 74.4c   [28]
Bagasse [Bmim] [Cl] + NaOH 110 12 12.73b   [28]
Polar wood [Emim] [OAc] + NaOH 110 12 8.72b    
Bamboo [Amim] [Cl] + NaOH 100 5 4.04b    
Corncob [Emim] [OAc]/H2O + NaOH 110   9.78b    
Corncob [Emim] [OAc]/DMF + NaOH     7.24b    
Corncob [Emim] [OAc]/DMSO + NaOH     19.5a   [48]
Corncob [Emim] [OAc]/DMAc + NaOH     32a    
Eucalyptus [Bmim] [Ace] + NaOH 120 3 37.3a    
Eucalyptus [Bmim] [Ace]/DMAc + NaOH     25.8a    
Eucalyptus [Bmim] [Ace]/Dioxane + NaOH     29.9a    
Eucalyptus [Bmim] [Ace]/Ethylacetate + NaOH     70   [28]
Eucalyptus [Bmim] [Ace]/Toluene + NaOH     74   [28]
Eucalyptus [Ch] [Lys]     21   [28]
Switchgrass [Ch] [Lys] 140 1      
Pine [Ch] [Lys]          

a Based on dry biomass; b based on Klason lignin; c based on the original lignin content in raw biomass.

3. Conclusions and Future Remarks

The exploitation of ILs in LC biomass treatment shows the tremendous potential in this research filed, especially within the context of the separation of lignin from LC biomass. The successful dissolution of lignin in ILs has broadened the sight when it comes to utilizing biomass for the production of biofuels, chemicals, and materials in a sense of technical and economic growth. The dependence of the ILs physical properties and their ability to solubilize LC biomass is considered important in the production of biochemicals. Due to its easily synthesizing process, various ILs can be used to design solvents with desired physicochemical properties that focus on the specific subcomponents of LC biomass.

To take into account the possible use in biorefinery scale is necessary for the practical considerations of pretreatment with ILs techniques. The results of experiments that have been carried out in relation to regeneration and the potential for recycling when it comes to pyridinium and pyrrolidinium-based PILs showed that the present dissolution processes that are using them could open the door to the diverse production of high-value products from lignin, including, binders, carbon fibers, phenolic compounds lignin-based polymers, and sorbents.

In all likelihood, lignin is a promising resource when it comes to replacing petroleum products in the chemical industry. Numerous studies have also shown there is undeniable potential for the depolymerization of lignin for the production of chemicals. However, these studies have mostly focused on experiments at a laboratory scale. The product characterization from the upgraded scale of lignin depolymerization can improve utilization of the lignin depolymerization process in the production of chemicals. Such an advance could afford what would be considered the foundation of biomass utilization and a green future.

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