Dissolution Of Lignin Research Articles

Computational Advances in Ionic Liquid Applications for Green Chemistry: A Critical Review of Lignin Processing and Machine Learning Approaches

The valorization and dissolution of lignin using ionic liquids (ILs) is critical for developing sustainable biorefineries and a circular bioeconomy. This review aims to critically assess the current state of computational and machine learning methods for understanding and optimizing IL-based lignin dissolution and valorization processes reported since 2022. The paper examines various computational approaches, from quantum chemistry to machine learning, highlighting their strengths, limitations, and recent advances in predicting and optimizing lignin-IL interactions. Key themes include the challenges in accurately modeling lignin’s complex structure, the development of efficient screening methodologies for ionic liquids to enhance lignin dissolution and valorization processes, and the integration of machine learning with quantum calculations. These computational advances will drive progress in IL-based lignin valorization by providing deeper molecular-level insights and facilitating the rapid screening of novel IL-lignin systems.

Study on the Remediation of Groundwater Nitrate Pollution by Pretreated Wheat Straw and Woodchips

Groundwater nitrate contamination poses a threat to both the ecological environment and human health. This study investigated the potential of using saturated Ca(OH)2 to pretreat wheat straw and woodchips, aiming to enhance their efficacy as carbon sources for denitrification. The optimization of pretreatment conditions, and the elucidation of underlying mechanisms were explored. The pretreatment process involved the dissolution of lignin and hemicellulose, exposure of the cellulose structure, reduction of hydrogen bonds within cellulose, hydrolysis of polymerized cellulose, and the formation of cracks and hierarchical structures on the surface of the carbon source. These alterations improved the attachment and utilization of microorganisms. The maximum enzymatic reducing sugar yields for wheat straw and woodchips were achieved at solid-liquid ratios of 1:40 and soaking times of 5 and 2 days, respectively. The response surface predicted the optimal pretreatment conditions for wheat straw to be a solid-liquid ratio of 1:88.1 and a soaking time of 8.2 hours. Alkaline treatment increased the denitrification rate of woodchips by fivefold and prevented the initial organic matter leaching rate of wheat straw, thereby reducing the risk of secondary pollution. The predominant microbial communities in all samples exhibited functions related to lignocellulose degradation and denitrification. The community composition of solid-phase carbon sources was found to be richer than that of liquid-phase carbon sources, and the pretreatment increased the abundance of lignocellulose degradation and denitrification functional microorganisms. The pretreatment liquid of wheat straw achieved the highest denitrification rate constant (0.43 h-1). Our result validated the feasibility of using the pretreatment liquid as a denitrification carbon source and presenting a novel approach for waste resource utilization.

Comprehensive analysis of lignin dimer dissolution microscopic mechanism in different aromatic-based deep eutectic solvent

Aromatic-based deep eutectic solvent (DES) is a novel kind of DES that can dissolve lignin efficiently. Density functional (DFT) calculation, molecular dynamics (MD) simulation and multivariate analysis were used to investigate the interaction mechanism of five aromatic-based DES on two lignin dimer models. The effects of dissolution temperature and the type of aromatic hydrogen bond donor (HBD) on the breaking bonds between β-O-4 and 5–5 substructural units or interacting with different functional groups on lignin were investigated. With the introduction of DES, the electrostatic interaction between Cl- and lignin was obvious, while the van der Waals interaction between HBD, Ch+ and lignin was obvious. Among all the aromatic-based DES, choline chloride/p-hydroxybenzoic acid (ChCl/PB) is considered to have efficient dissolution effect. In the process of lignin dissolution, γ-OH was the preferred site for PB and Cl- acting on the lignin dimer (β-O-4), and the proportion of hydrogen bonding with γ-OH is 40 %. It was distributed around the lignin dimer (β-O-4) at 0.28–0.32 nm, and the total interaction energy was −4041.1452 kJ/mol. This study provided novel insights and theoretical basis for the preparation of renewable DES using aromatic components.

Pretreatment of Vine Shoot Biomass by Choline Chloride-Based Deep Eutectic Solvents to Promote Biomass Fractionation and Enhance Sugar Production.

Vine shoots hold promise as a biomass source for fermentable sugars with efficient fractionation and conversion processes. The study explores vine shoots as a biomass source for fermentable sugars through pretreatment with two deep eutectic solvents mixtures: choline chloride:lactic acid 1:5 (ChCl:LA) and choline chloride:ethylene glycol 1:2 (ChCl:EG). Pretreatment conditions, such as temperature/time, solid/liquid ratio, and biomass particle size, were studied. Chemical composition, recovery yields, delignification extent, and carbohydrate conversion were evaluated, including the influence of washing solvents. Temperature and particle size notably affected hemicellulose and lignin dissolution, especially with ChCl:LA. Pretreatment yielded enriched cellulose substrates, with high carbohydrate conversion rates up to 75.2% for cellulose and 99.9% for xylan with ChCl:LA, and 54.6% for cellulose and 60.2% for xylan with ChCl:EG. A 50% acetone/water mixture increased the delignification ratios to 31.5%. The results underscore the potential of this pretreatment for vine shoot fractionation, particularly at 30% solid load, while acknowledging the need for further process enhancement.

Urea-lactic acid as efficient lignin solvent and its practical utility in sustainable electrospinning

The development of lignin-based materials presents a promising avenue for advancing green chemistry and mitigating environmental impact. However, the key challenge lies in the processability of lignin, which significantly affects its practical applications. Addressing the issues related to lignin's complex structure, variability, and reactivity is crucial for optimizing its incorporation into high-performance materials. Therefore, in this study we explore the efficacy of a urea-lactic acid-based deep eutectic solvent (ULA) for the dissolution of kraft lignin, aiming to enhance its practical utility in sustainable electrospinning processes, for the first time. Results of elemental analysis, IR and 2D NMR spectroscopy, provide crucial insights into the structural properties of the regenerated material post-DES treatment. The findings confirm a high lignin recovery rate, reaching up to 96.6 % for samples dissolved at 100°C. Additionally, 2D NMR analysis indicates that the process leads to partial esterification of lignin with lactate ions. The ability of the studied DES to effectively solubilize lignin underscores its potential as an efficient lignin solvent and facilitates the fabrication of lignin-based nanofibers via electrospinning. The incorporation of this DES in electrospinning processes promises significant advancements in the development of sustainable, lignin-derived materials and offers a green alternative for production of high-performance nanofibers. Preliminary results of electrochemical impedance spectroscopy and galvanostatic charge/discharge measurements confirm that the EDLC with prepared hydrogel electrolyte demonstrates attractive electrochemical properties (specific capacitance, CSP = 95 F g–1; series resistance RS = 2.2 Ω; charge transfer resistance, RCT = 1.6 Ω), which are comparable with the reference cell based on a commercial glass fibre separator. Hence, the DES-assisted-electrospinned lignin membrane can be viewed as a potential gel electrolyte matrix for practical use in construction of sustainable energy storage devices.

Boosting Lignin Dissolution and Biomass Fractionation by Innovative Alkaline Deep Eutectic Solvents

Boosting Lignin Dissolution and Biomass Fractionation by Innovative Alkaline Deep Eutectic Solvents

New insights into kinetics and mechanisms of acid sulphite delignification of Eucalyptus globulus wood

The kinetics of Eucalyptus globulus wood delignification in Mg-base acid sulphite pulping of dissolving pulp was studied using a pilot-scale batch digester simulating the industrial process. The behavior of lignin during impregnation, heating-up and bulk delignification at the final temperature was evaluated by the analysis of acid-insoluble lignin in wood and wood residue after pulping. The dynamics of lignin dissolution was followed by its structural analysis in solid residues and in solution by wet chemistry and 1D and 2D nuclear magnetic resonance (NMR) spectroscopy. About 30 % and 20 % of the lignin were removed in the impregnation and heating-up pulping steps, respectively. About 45 % of the lignin was removed at the final pulping temperature in bulk and 3 % in the residual delignification stages. The kinetics of bulk delignification followed a pseudo-first-order kinetics with an effective activation energy of 138.4 kJ/mol in the temperature range of 140–148 °C. Bulk delignification follows an undefined overall order in the hydrogen and bisulfite ions and depended on the partial pressure of SO2 at ca. 0.60 order within the range of combined SO2 in pulping acid of 1.14–1.66 % and total SO2 loads of 6.2–7.0 %. Minimum degree of lignin sulphonation to be dissolved in the pulping liquor was suggested to be about 0.35 sulphonic groups per one phenyl propane unit. Lignin removal during pulping showed dependence on its location in different morphological parts of the fibers and related structural characteristics, which were discussed accordingly. A role of the polysaccharide complex in the accessibility of lignin was highlighted. A noticeable cleavage of β-O-4 linkages occurred in lignin already dissolved in pulping liquor at the end of cooking.

Role of Deep Eutectic Solvent Precursors as Hydrotropes: Unveiling Synergism/Antagonism for Enhanced Kraft Lignin Dissolution.

Lignin holds significant potential as a feedstock for generating valuable aromatic compounds, fuels, and functional materials. However, achieving this potential requires the development of effective dissolution methods. Previous works have demonstrated the remarkable capability of hydrotropes to enhance the aqueous solubility of lignin, an amphiphilic macromolecule. Notably, deep eutectic solvents (DESs) have exhibited hydrotropic behavior, significantly increasing the aqueous solubility of hydrophobic solutes, making them attractive options for lignin dissolution. This study aimed at exploring the influence of hydrogen bond acceptors (HBAs) and hydrogen bond donors (HBDs) on the performance of DESs as hydrotropes for lignin dissolution, while possible dissolution mechanisms in different water/DES compositions were discussed. The capacity of six alcohols (glycerol, ethylene glycol, 1,3-propanediol, 1,4-butanediol, 1,5-pentanediol, and 1,6-hexanediol) and cholinium chloride to enhance the solubility of Kraft lignin in aqueous media was investigated. A correlation between solubility enhancement and the alkyl chain length of the alcohol was observed. This was rationalized upon the competition between hydrotrope-hydrotrope and solute-hydrotrope aggregates with the latter being maximized for 1,4-butanediol. Interestingly, the hydrotropic effect of DESs on lignin solubility is well represented by the independent sum of the dissolving contributions from the corresponding HBAs and HBDs in the diluted region. Conversely, in the concentrated region, the solubility of lignin for a certain hydrotrope concentration was always found to be higher for the pure hydrotropes rather than their combined HBA/HBD counterparts.

Unveiling the ability of protic and aprotic ionic liquids to dissolve and modify Kraft lignin

Lignin, a renewable macromolecule abundant in lignocellulosic biomass, holds significant promise as a renewable source for producing biofuels, biomaterials, and fine chemicals, offering a potential avenue to reduce dependence on petroleum-derived products. However, the lignin complex structure poses challenges for its effective utilization, often requiring some special treatments. In recent decades, ionic liquids (ILs) have been pointed out as promising candidates for lignin processing due to their appealing properties, which include low vapor pressure/flammability, high chemical and thermal stability, and efficacy as lignin solvents. ILs may be categorized as protic (PILs) or aprotic ionic liquids (AILs), and these two classes offer distinct advantages. PILs are readily synthesized by mixing an acid and a base in stoichiometric proportions, forming a mixture containing neutral species that remain in equilibrium with cations and anions. In contrast, AILs present cations with enduring positive charges and are not in equilibrium with their precursors as the PILs, though AILs are frequently more expensive and challenging to produce. Within the biorefinery context, the ability to dissolve Kraft lignin is pivotal for developing new strategies and technologies. Moreover, chemical transformations may occur during lignin dissolution in IL solutions. In this study, the solubility of Kraft lignin was evaluated in four neat imidazolium-based AILs, five neat pyrrolidinium-based PILs, and in aqueous solutions of these ILs, at 313.2 K. The highest solubility value ((77.71 ± 1.03) wt%) was observed for pyrrolidinium octanoate (PIL), while 1-butyl-3-methylimidazolium methyl sulfate exhibited the highest solubility ((73.93 ± 1.27) wt%) among the studied AILs. Whenever possible, the solubilities measured in the present work were critically compared with data available in the literature. Finally, lignin recovered from the IL solutions was analyzed by Gel Permeation Chromatography (GPC), Fourier Transform Infrared (FTIR), and Nuclear Magnetic Resonance (NMR) spectroscopy to assess the solvent ability to induce structural modifications in this macromolecule. The analysis revealed that ILs effectively cleaved β-O-4 linkages in lignin molecules, and concurrent condensation reactions might increase the precipitated lignin molecular weight.

Understanding Lignin Dissolution with Urea and the Formation of a Lignin Nano-Aggregate: A Multiscale Approach.

This study employs a combined computational and experimental approach to elucidate the mechanisms governing the interaction between lignin and urea, impacting lignin dissolution and subsequent aggregation behavior. Molecular dynamics (MD) simulations reveal how the urea concentration and temperature influence lignin conformation and interactions. Higher urea concentrations and temperatures promote lignin dispersion by disrupting intramolecular interactions and enhancing solvation. Density functional theory (DFT) calculations quantitatively assess the interaction energy between lignin and urea, supporting the findings from MD simulations. Anti-solvent precipitation demonstrates that increasing the urea concentration hinders the self-assembly of lignin nanoclusters. The findings provide valuable insights for optimizing lignin biorefinery processes by tailoring the urea concentration and temperature for efficient extraction and dispersion. Understanding the influence of urea on lignin behavior opens up avenues for designing novel lignin-based materials with tailored properties. This study highlights the potential for the synergetic application of MD simulations and DFT calculations to unravel complex material interactions at the atomic level.

Holistic investigation of structural evolution in corn stover lignin under pretreatment with varying γ-valerolactone concentrations

Until now, research on green and sustainable γ-valerolactone (GVL) pretreatment has predominantly centered on component separation efficiency, with limited attention given to the lignin structure. Nonetheless, the lignin's structure is considerably affected by the fractionation, consequently influencing its potential valorization. Herein, we conducted a holistic investigation of the structural evolution of two fractions of lignin in corn stover, obtained under pretreatment with varying GVL concentrations: GVL lignin (GVLL) originated from pretreatment liquor and cellulolytic enzyme lignin (CEL) separated from pretreated residue. Our findings indicated a general positive correlation between the molecular weight and polydispersity index of both GVLL and CEL with the increasing GVL concentration. This phenomenon is attributed to the enhanced lignin dissolution and relocation as the GVL concentration increases. Moreover, higher GVL concentrations also increased the acidity of reaction system, leading to degradation of β-O-4 linkages from 45.2 to 34.9 and 57.6 to 37.9 per 100 aromatic units in GVLL and CEL, respectively. Compared to CEL, GVLL exhibited a more remarkable phenolics yield (33.7% vs. 22.2%) during hydrodeoxygenation due to its superior purity and lower degree of polymerization. Recycling studies demonstrated the stability of GVL at lower concentrations. These findings provide valuable insights for optimizing GVL pretreatment systems.

Selective extraction of cellulose from xylose residue using ionic liquids/DMSO: COSMO-RS prediction and experimental verification

Efficiently dissolving and separating cellulose from xylose residue is beneficial to realize the high added-value of lignocellulosic waste. In this work, theoretical prediction by using COSMO-RS and practical experiments were combined to investigate the extraction selectivity of ionic liquids (ILs) for cellulose and lignin. Two imidazolium-based ILs, 1-ethyl-3-methylimidazolium diethylphosphate ([Emim]DEP) and 1-allyl-3-methylimidazolium chloride ([Amim]Cl), were screened out from 425 ILs. These ILs were subsequently mixed with dimethyl sulfoxide (DMSO) to dissolve and separate cellulose from xylose residue. The cellulose extraction efficiency of [Emim]DEP/DMSO were optimized by regulating the content of xylose residue, dissolution temperature and time. As the cellulose content was 1.2 wt%, the dissolution temperature of 80 °C, and the dissolving time of 120 min, the cellulose extraction rate of xylose residue could reach as high as 99.3% in [Emim]DEP/DMSO, which is higher than that in [Amim]Cl/DMSO (95.4%). The higher cellulose and lower lignin dissolution capacities of [Emim]DEP indicated that [Emim]DEP was a promising solvent to realize the conversion and utilization of cellulose in agro-industrial residues. In addition, [Emim]DEP presents constant dissolution capacity even it was recycled for five times. Furthermore, the produced xylose residue cellulose film (XRCF) displayed a homogeneous and smooth morphology with a tensile strength of 55.9 MPa, which had great potential in packaging.

Robust Oxidase-Mimetic Supramolecular Nanocatalyst for Lignin Biodegradation.

Enzymatic catalysis presents an eco-friendly, energy-efficient method for lignin degradation. However, challenges arise due to the inherent incompatibility between enzymes and native lignin. In this work, we introduce a supramolecular catalyst composed of fluorenyl-modified amino acids and Cu2+, designed based on the aromatic stacking of the fluorenyl group, which can operate in ionic liquid environments suitable for the dissolution of native lignin. Amino acids and halide anions of ionic liquids shape the copper site's coordination sphere, showcasing remarkable catechol oxidase-mimetic activity. The catalyst exhibits thermophilic property, and maintains oxidative activity up to 75 °C, which allows the catalyzed degradation of the as-dissolved native lignin with high efficiency even without assistance of the electron mediator. In contrast, at this condition, the native copper-dependent oxidase completely lost its activity. This catalyst with superior stability and activity offer promise for sustainable lignin valorization through biocatalytic routes compatible with ionic liquid pretreatment, addressing limitations in native enzymes for industrially relevant conditions.

Sulfomethylation reactivity enhanced the Fenton oxidation pretreatment of bamboo residues for enzymatic digestibility and ethanol production.

Bamboo is considered a renewable energy bioresource for solving the energy crisis and climate change. Dendrocalamus branddisii (DB) was first subjected to sulfomethylation reaction at 95°C for 3h, followed by Fenton oxidation pretreatment at 22°C for 24h. The synergistic effect of combined pretreatment dramatically improved enzymatic digestibility efficiency, with maximum yield of glucose and ethanol content of 71.11% and 16.47g/L, respectively, increased by 4.7 and 6.11 time comparing with the single Fenton oxidation pretreatment. It was found that the hydrophobicity of substrate, content of surface lignin, degree of polymerization, and specific surface area have significant effects on the increase of enzymatic saccharification efficiency. It also revealed that sulfomethylation pre-extraction can improve the hydrophilicity of lignin, leading to the lignin dissolution, which was beneficial for subsequent Fenton pretreatment of bamboo biomass. This work provides some reference for Fenton oxidation pretreatment of bamboo biomass, which can not only promote the utilization of bamboo in southwest China, but also enhances the Fenton reaction in the bamboo biorefinery.

Sequential catalytic lignin valorization and bioethanol production: an integrated biorefinery strategy

BackgroundThe effective valorization of lignin and carbohydrates in lignocellulose matrix under the concept of biorefinery is a primary strategy to produce sustainable chemicals and fuels. Based on the reductive catalytic fractionation (RCF), lignin in lignocelluloses can be depolymerized into viscous oils, while the highly delignified pulps with high polysaccharides retention can be transformed into various chemicals.ResultsA biorefinery paradigm for sequentially valorization of the main components in poplar sawdust was constructed. In this process, the well-defined low-molecular-weight phenols and bioethanol were co-generated by tandem chemo-catalysis in the RCF stage and bio-catalysis in fermentation stage. In the RCF stage, hydrogen transfer reactions were conducted in one-pot process using Raney Ni as catalyst, while the isopropanol (2-PrOH) in the initial liquor was served as a hydrogen donor and the solvent for lignin dissolution. Results indicated the proportion of the 2-PrOH in the initial liquor of RCF influenced the chemical constitution and yield of the lignin oil, which also affected the characteristics of the pulps and the following bioethanol production. A 67.48 ± 0.44% delignification with 20.65 ± 0.31% of monolignols yield were realized when the 2-PrOH:H2O ratio in initial liquor was 7:3 (6.67 wt% of the catalyst loading, 200 °C for 3 h). The RCF pulp had higher carbohydrates retention (57.96 ± 2.78 wt%), which was converted to 21.61 ± 0.62 g/L of bioethanol with a yield of 0.429 ± 0.010 g/g in fermentation using an engineered S. cerevisiae strain. Based on the mass balance analysis, 104.4 g of ethanol and 206.5 g of lignin oil can be produced from 1000 g of the raw poplar sawdust.ConclusionsThe main chemical components in poplar sawdust can be effectively transformed into lignin oil and bioethanol. The attractive results from the biorefinery process exhibit great promise for the production of valuable biofuels and chemicals from abundant lignocellulosic materials.

Unraveling the mechanisms underlying lignin and xylan dissolution in recyclable biphasic catalytic systems

Despite the exceptional performance of recyclable biphasic pretreatment systems (i.e., p-toluenesulfonic acid (TsOH)/pentanol, H2SO4/butanol, and AlCl3/MTHF) in the holistic fractionation of lignocellulosic biomass (LCB), there remains a significant gap in understanding of the intricate mechanisms governing the rapid dissolution of lignin and xylan from LCB. This study conducts comparative analyses using laboratory experiments and computational simulations to gain insights into the mechanism behind removing lignin and xylan in these systems. Under identical pretreatment conditions (140 °C, 45 min), three systems exhibited distinct levels of delignification and xylan removal. TsOH/pentanol showcased the highest levels of both delignification (83.3%) and xylan removal (98.1%), followed by H2SO4/butanol (77.9% delignification and 83.0% xylan removal), and AlCl3/MTHF (73.5% delignification and 97.2% xylan removal). Lignin characterization revealed that TsOH/pentanol and AlCl3/MTHF lignin samples boasted well-preserved β-O-4 bonds (42.4/100 Ar, 40.4/100 Ar, respectively), uniform molecular weights, and <1% sugar content. This led to high yields of phenolic monomers (TsOH/pentanol, 33.9%; AlCl3/MTHF, 33.7%) after catalytic hydrogenolysis of lignin. Furthermore, mechanistic analyses revealed that the TsOH/pentanol and AlCl3/MTHF systems exhibited the most significant interaction energy formation with the lignin model (veratrylglycerol-b-guaiacyl ether) and D-xylan model due to robust hydrogen bonding interactions, yielding energy values of −2460 kJ/mol and −2385 kJ/mol, respectively. These interactions could play pivotal roles in accomplishing notable lignin and xylan extraction.

Water effect on the characterization of 1-butyl-3-methylimidazolium hydrogen sulfate and lignin dissolution

ABSTRACT Lignin dissolution plays an important role in the conversion process of lignin. This work focused on the lignin dissolution in a binary mixture of 1-butyl-3-methylimidazolium hydrogen sulfate([BMIM]HSO4) and water. To understand the lignin dissolution behavior in the binary mixture of [BMIM]HSO4/H2O, the molecular interactions of [BMIM]HSO4 and H2O were first investigated by simple methods based on the viscosity and UV spectra. Then three different lignin samples, enzymatic hydrolysis lignin, alkali lignin, and organosolv Lignin, were employed to investigate the dissolution ability of [BMIM]HSO4/water with different mass fraction of [BMIM]HSO4([BMIM]HSO4%). The molecular interactions and lignin solubility of [BMIM]HSO4/H2O strongly depended on the mass fraction of [BMIM]HSO4([BMIM]HSO4%). A turning point for the formation of bi-continuous system at [BMIM]HSO4% of 63% was observed by the changing trend of viscosity and UV absorption. [BMIM]HSO4/H2O with 60-90% of [BMIM]HSO4% had excellent ability to dissolve EHL, and achieved the maximum value at 70% of [BMIM]HSO4%. It was indicated that the bi-continuous [BMIM]HSO4/H2O was the most effective in lignin dissolution. Lignin was regenerated with a recovery rate of 94.29%. Compared the regenerated lignin and the raw lignin, [BMIM]HSO4 altered the arrangement structure of lignin without no changes in the chemical structures. This study provided ideas for the process design of lignin dissolution and conversion in the [BMIM]HSO4/H2O system.

Enhancement of mechanical and flame-retardant properties of Acacia hybrid through the treatment of a combination of styrene-acrylic copolymer and sodium silicate

The mechanical and flame-retardant properties of Acacia hybrid wood were studied through the treatment of an aqueous solution containing a styrene-acrylic copolymer (SC) and sodium silicate (SS). The results showed a significant increase in the mechanical properties of SC/SS-treated wood. Specifically, the modulus of rupture (MOR) and modulus of elasticity (MOE) improved by up to 71.54% and 53.65%, respectively. The surface hardness of the cross-section and radial section also increased by 37.24% and 46.65%, respectively. The treated wood’s weight percentage gain (WPG) reached up to 23.31%. The largest leaching rate (LR) of treated wood was only 8.01%, suggesting this treatment has obvious effects in fixing the SS in the wood. However, it did not cause positive bulking efficiency (BE) and anti-swelling efficiency (ASE). The incorporation of SS with SC resulted in the decomposition of polysaccharides at a lower temperature while increasing the limiting oxygen index (LOI), which was 34.95% higher than that of untreated wood, making it more difficult to ignite. Scanning electron microscopy (SEM) results showed that the SC/SS deposited in the cell lumina after polymerization, but significant structural changes occurred, including vessel and cell wall deformation due to the partial dissolution of hemicellulose and lignin from the cell wall in the alkaline solution. The results of this study demonstrate the feasibility of applying the SC/SS combination treatment to wood in practical applications.

Lactic Acid-Proline Solvent Pretreatment of CS: Effects of Process Variables on Glucan, Xylan, and Lignin Composition

The aim of this study is to investigate the effect of temperature, duration, and water dilution on the composition of glucan, xylan, and lignin in cowpea shells (CS) pretreated with a neat and diluted Lactic acid-proline solvent. The composition of glucan, xylan, and lignin was analyzed using the NREL method. The highest xylan removal (12%) was achieved after a 6-hour pretreatment at 150°C, while 11.35% lignin removal was observed after 5 hours at the same temperature. The most significant increase in glucan content, reaching 78.3 %, was observed after 4 hours at 150°C using a 2.5% (w/w) water-diluted solvent. Comparing the effect of the neat solvents and diluted solvents it can be concluded that while the neat solvent promoted the dissolution of xylan and lignin, the addition of water preserved glucan from the harshness of the pretreatment. Therefore, the decision to dilute a natural deep eutectic solvent before its application in biomass pretreatment depends on the desired product from biomass fractionation (lignin or a carbohydrate-rich material) and pretreatment temperature. These findings provide a foundation for further investigations into optimizing the entire process.

Insight into the dissolution behaviour and rheological characterisation of lignin in 1-butyl-3-methylimidazole bisulphate-ethanol system

ABSTRACT Lignin dissolution and the fluid behaviour of reaction systems play important roles in the conversion rate of lignin. This study investigated the solubility of enzymatic hydrolysis lignin (EHL) in 1-butyl-3-methylimidazole bisulphate ethanol solutions ([BMIM]HSO4/ethanol) and the dynamic shear rheological characterisation of EHL-[BMIM]HSO4/ethanol. Different with [BMIM]HSO4/water, [BMIM]HSO4/ethanol exhibited excellent abilities to dissolve EHL at [BMIM]HSO4% 20%–90%, with the maximum EHL solubility obtained at 40%–70%. The dynamic shear rheological characterisation strongly depended on temperatures, [BMIM]HSO4% and EHL%, exhibited as pseudoplastic fluid at higher [BMIM]HSO4% and EHL%, and Dilatant fluid at lower [BMIM]HSO4% and EHL%. Adjusting an appropriate [BMIM]HSO4% and EHL%, EHL-[BMIM]HSO4/ethanol was Newtonian fluid with the viscosity stable. EHL was regenerated from EHL-[BMIM]HSO4/ethanol without obvious changes in the chemical structure and thermal behaviour. This study provided ideas for the design of the [BMIM]HSO4/ethanol system and the optimisation of conversion processes for the economic utilisation of lignin.