Conversion of Cellulose and Lignin Residues into Transparent UV-Blocking Composite Films.

The valorization of cellulose and lignin residues in an integrated biorefinery is of great significance to improve the overall economics but has been challenged by their structural recalcitrance, especially for lignin residue. In this work, a facile chemical conversion route to fabricating functional UV-blocking cellulose/lignin composite films through a facile dissolution-regeneration process using these biomass residues was proposed. Three representative lignin residues, i.e., aspen and poplar wood lignin, and corn stover (CS) lignin were assessed for their feasibility for the film fabrication. The UV-blocking performance of the composite films were comparatively investigated. Results showed that all these three lignin residues could enhance the UV-blocking property of the composite films, corresponding to the reduction in the optical energy band gap from 4.31 to 3.72 eV, while poplar lignin had a considerable content of chromophores and showed the best UV-blocking enhancement among these three assessing lignins. The enhancement of UV-blocking property was achieved without compromising the visible-light transparency, mechanical strength and thermal stability of the composite films even at 4% lignin loading. This work showed the high promise of integrating biomass residue conversion into lignocellulose biorefinery for a multi-production purpose.

Critical parameters to standardize the size and concentration determination of nanomaterials by nanoparticle tracking analysis.

The size and concentration are critical for the diagnostic and therapeutic applications of nanomaterials but the accurate measurement remains challenging. Nanoparticle tracking analysis (NTA) is widely used for size and concentration determination. However, highly repeatable standard operating procedures (SOPs) are absent. We adopted the "search-evaluate-test" strategy to standardize the measurement by searching the critical parameters. The particles per frame are linearly proportional to the sample concentration and the measured results are more accurate and repeatable when the concentration is 108-109 particles/ml. The optimal detection threshold is around 5. The optimal camera level is such that it allows clear observation of particles without diffractive rings and overexposure. The optimal speed is ≤ 50 in AU and âˆ¼ 10 µl/min in flow rate. We then evaluated the protocol using polydisperse polystyrene particles and we found that NTA could discriminate particles in bimodal mixtures with high size resolution but the performance on multimodal mixtures is not as good as that of resistive pulse sensing (RPS). We further analyzed the polystyrene particles, SiO2 particles, and biological samples by NTA following the SOPs. The size and concentration measured by NTA differentially varies to those determined by RPS and transmission electron microscopy.

Lewis acid/base mediated deep eutectic solvents intensify lignocellulose fractionation to facilitate enzymatic hydrolysis and lignin nanosphere preparation.

In this work, Lewis acids (FeCl3, AlCl3) and bases (Na2CO3, Na2SO3) were incorporated into a neutral deep eutectic solvent (DES, choline chloride/glycerin) to intensify the lignocellulose fractionation. The efficiency of fractionation in terms of the maximum delignification rate (89.7 %) and well-pleasing cellulose saccharification (100 %) could be achieved by the Lewis acid-mediated DES. An in-depth insight of the evolution of lignin structure revealed that Lewis acid-mediated DES could cleave the ß-O-4 linkages efficiently to achieve a high yield lignin fragments. Meanwhile, the lignin fragments with the enhanced amphiphilic properties facilitate the preparation of lignin nanospheres (LNSs) via the self-assembly process. The resultant LNSs extracted by Lewis acid-mediated DES exhibited an excellent thermal stability, and enhanced antibacterial capacity, which were associated with the phenolic OH content. However, the extracted lignin by Lewis base-mediated DES was mainly attributed to the cleavage of lignin-carbohydrate complexes bond, especially the lignin-carbohydrate ester bond, which retained more ether bonds and a relatively complete structure. This study illuminated the different mechanisms of lignin extraction and the structural evolution of lignin from Lewis acid/base-mediated DES, and provided guidance to select suitable fractionation techniques for upgrading the downstream products.

Two all-biomass cellulose/amino acid spherical nanoadsorbents based on a tri-aldehyde spherical nanocellulose II amino acid premodification platform for the efficient removal of Cr(VI) and Cu(II).

Adsorbents consisting of spherical nanoparticles exhibit superior adsorption performance and hence, have immense potential for various applications. In this study, a tri-aldehyde spherical nanoadsorbent premodification platform (CTNAP), which can be grafted with various amino acids, was synthesized from corn stalk. Subsequently, two all-biomass spherical nanoadsorbents, namely, cellulose/l-lysine (CTNAP-Lys) and cellulose/L-cysteine (CTNAP-Cys), were prepared. The morphologies as well as chemical and crystal structures of the two adsorbents were studied in detail. Notably, the synthesized adsorbents exhibited two important characteristics, namely, a spherical nanoparticle morphology and cellulose II crystal structure, which significantly enhanced their adsorption performance. The mechanism of the adsorption of Cr(VI) onto CTNAP-Lys and that of Cu(II) onto CTNAP-Cys were studied in detail, and the adsorption capacities were determined to be as high as 361.69 (Cr(VI)) and 252.38 mg/g (Cu(II)). Using the proposed strategy, it should be possible to prepare other all-biomass cellulose/amino acid spherical nanomaterials with high functional group density for adsorption, medical, catalytic, analytical chemistry, corrosion, and photochromic applications.

Stress distribution on the mandibular condyle and the distraction area in distraction osteogenesis by finite element analysis.

PURPOSE: Many 3-dimensional (3-D) finite element analysis (FEA) models based on the virtual simulation have been constructed to explore the stress distribution during distraction osteogenesis (DO). The aim of this study is to achieve a better understanding of the biomechanical feature of mandible during DO procedure. MATERIALS AND METHODS: Using CT image data of a goat mandible that already has been elongated for 10 mm, an anatomical 3D model was reconstructed. This model was imported into MSC.Patran for monitoring mechanical parameters, including Von-Mises stress, max-principal stress, and mix-principal stress, on the distraction area and the mandibular condyle. RESULTS: The computed result showed special stress distribution on 9 slopes of the condyle and 3 cross-sections of the distraction area. From 0.8 MP to 17.2 MP, a dramatic increase in Von-Mises stress was discovered on the right side of the condyle compared with the left side. From 22.6 MP to 0.9 MP on the distraction area, Von-Mises stress decreased from the central zone to the peripheral zone gradually. CONCLUSIONS: During the process of mandibular DO, the special stress distribution may be an important factor on the physiopathological change of the mandibular condyle and the generation of new bone in the distraction area. The correlations between the value of the stress and physiopathological changes during DO process should be clarified in future research.

Acidic deep eutectic solvent assisted mechanochemical delignification of lignocellulosic biomass at room temperature.

Lignocellulosic biomass is the most abundant natural polymer on Earth, but the efficient fractionation and refinery of all its components remain challenging. Acidic deep eutectic solvents refining is a promising method, while it is likely to cause lignin condensation and carbohydrates degradation, especially at server operation conditions. Here we propose the use of acidic deep eutectic solvent (DES), choline chloride/p-toluenesulfonic acid assisted mechanochemical pretreatment (DM) for efficient lignocellulose fractionation at mild condition. Four representative lignocellulose, wheat straw, moso bamboo, poplar wood and pine wood were selected at varied milling time (3, 6 h) to assess the fractionation ability of this strategy. This DM pretreatment demonstrated a rather high cellulose retentions (∼90 %) and extent of delignification for wheat straw and bamboo biomass, which corresponds to a high extent of enzymatic hydrolysis (∼75.5 %) for sugar platform pursuing. The extracted lignin showed rather high content of ß-O-4' leakages due to the swelling effect of deep eutectic solvent and mild operation conditions. This work provided a promising strategy to fractionate lignocellulose using deep eutectic solvents with the goal of simultaneous cellulose hydrolysis and reactive lignin obtaining that is usually difficult to realize using traditional chemical fractionation approach.

The coupling effects between acid-catalyzed hydrothermal pretreatment and acidic/alkaline deep eutectic solvent extraction for wheat straw fractionation.

Mild hydrothermal pretreatment (HP) integrating with solvent extraction is a promising two-step technique to enhance the overall lignin and carbohydrate output for lignocellulose fractionation. This work comparatively assessed the coupling effect between mild HP (the first step) and the emerging acidic choline chloride-natural acid or alkaline choline hydroxide based deep eutectic solvents (DES, the second step) for wheat straw fractionation. It was shown HP with 0.3% p-toluenesulfonic acid (p-TsOH) catalyst achieved a good compromise between complete hemicellulose removal (nearly 100%) and high cellulose recovery (99.2%). While choline hydroxide based DES showed better coupling effect with HP than choline chloride-natural acid DES, corresponding to 75.6 and 31.2% lignin removal respectively. It was proposed that the alkaline DES enhanced lignocellulose swelling the lignin phenolic hydroxyl groups deprotonation and thus facilitating lignin solubilization despite of its condensation at HP. Therefore, the alkaline DES resulting cellulose-rich fraction exhibited higher potential for further processing.

Vibration-enhanced disposable electroanalytical platform for selective analysis of tryptophan in fruits based on molecular imprinting.

Although electrochemical detection based on molecular imprinting polymers (MIP) could dramatically improve the selectivity, the procedure is time-consuming because of the essential incubation step. In addition, current MIP electrochemical detections were not suitable for analysis of microliter-level sample solutions, limiting their applications for real samples. This investigation aims at applying vibration to enhance efficiency of MIP electrochemical detection of 20 µL sample solutions. MIP analysis of Tryptophan (Trp) was used as the model with disposable MIP electrodes prepared by electrochemical polymerization of o-phenylenediamine on carbon ink coated on stainless steel sheets. The MIP electrode was integrated in a 3D-printed analytical device for vibration-enhanced electrochemical detection of Trp. Our results showed that this vibration-enhanced strategy could significantly increase electrochemical responses of Trp at the same incubation time. Such improvement might be attributed to the enhanced mass transfer at the surface of the working electrode brought by vibration. It needs to be emphasized that this strategy is suitable for analysis of sample solutions with the volume of microliters, which is superior to normal stirring in MIP electrochemical detection. Our approach could be successfully utilized for differentiation of Trp in different fruits, opening more opportunities for MIP electrochemical detection of real samples. The enhanced efficiency by vibration could pave foundation for extensive practical MIP detection of sample solutions at the level of microliters.

Biochar produced by combining lignocellulosic feedstock and mushroom reduces its heterogeneity.

To reduce the feedstock-sourced heterogeneity of biochar, mushrooms, cultivated from lignocellulosic feedstocks (LFs), were used as precursors for biochar preparation. The coefficient of variation (CV) was adopted to show the homogeneity changes. In contrast to LFs, mushrooms produced relatively lower CVs in terms of elemental and proximate analysis. Furthermore, the CV of H/C (9.20%) and O/C (13.32%) of mushroom-based biochars (MRBCs) was lower than that of LF-based biochars (LFBCs), suggesting more homogeneous aromaticity and hydrophilicity. The relatively lower CV of the volatile matter (0.87%), fixed carbon (0.45%), and ash (2.44%) of MRBCs suggested an improvement in the homogeneity of chemical components. The homogenized physical structure was reflected in the lack of a difference in pore characteristics of MRBCs. The lower CVs (1.89-14.82%) for the pollutant adsorption of MRBCs, implied more stable performance. In conclusion, converting LFs to mushrooms reduced the precursor's heterogeneity, consequently homogenizing the biochar's properties and performance.

Understanding and characteristics of coagulation removal of composite pollution of microplastic and norfloxacin during water treatment.

Water composite pollution is still a great challenge in the field of water treatment. Especially for microplastic (MP), as an emerging pollutant, its wide distribution in water and persistent eco-environmental influence have received great concerns in recent years. Nevertheless, the removal characteristics and mechanism of conventional coagulation on MP composite pollution is quite insufficient. In this study, the coagulation removal performance and mechanisms of MP (polyethylene, PE) and norfloxacin (NOR) was investigated by polyaluminium chloride (PAC) and anionic polyacrylamide (APAM). Compared with single system, the removal efficiency of PE was significantly improved (>99.0%) under plateau stage in composite system, while the removal efficiency of NOR was slightly decreased to around 42% regardless of the addition of APAM. The scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), zeta potential and One-way analysis of variance (ANOVA) of experimental data were used to explore the coagulation mechanisms. The results demonstrated that the removal of individual PE and NOR was mainly controlled by charge neutralization and sweep flocculation by PAC and APAM, and adsorption by formation of Al-NOR complex, respectively. Importantly, in composite system, the removal of PE was enhanced not only by the stronger charge neutralization but also the adsorption via the formation of PE-NOR-Al complex. Furthermore, the removal efficiency of PE and NOR in neutral and weak alkaline conditions was higher than that in weak acidic or strong alkaline conditions. The presence of metal ions and humic acid had obvious inhibition and promoting effects on the removal efficiency of PE and NOR. This study can provide a new perspective on fundamental understanding in characteristics and mechanisms of MP composite pollutants removed by coagulation.

A novel way to facilely degrade organic pollutants with the tail-gas derived from PHP (phosphoric acid plus hydrogen peroxide) pretreatment of lignocellulose.

The abundantly released tail-gas from lignocellulose pretreatment with phosphoric acid plus hydrogen peroxide (PHP) was found to accelerate the aging of latex/silicone textural accessories of the pretreatment device. Inspired by this, tail-gas was utilized to control organic pollutants. Methylene blue (MB), as a model pollutant, was rapidly decolorized by the tail-gas, and oxidative degradation was substantially proven by full-wavelength scanning with a UV-visible spectrometer. The tail-gas from six typical lignocellulosic feedstocks produced 68.0-98.3% MB degradation, suggesting its wide feedstock compatibility. Three other dyes, including rhodamine B, methyl orange and malachite green, obtained 97.5-99.5% degradation; moreover, tetracycline, resorcinol and hexachlorobenzene achieved 73.8-93.7% degradation, suggesting a superior pollutant compatibility. In a cytotoxicity assessment, the survival rate of the degraded MB was 103.5% compared with 80.4% for the untreated MB, implying almost no cytotoxicity after MB degradation. Mechanism investigations indicated that the self-exothermic reaction in PHP pretreatment drove the self-generated peroxy acids into tail-gas. Moreover, it heated the pollutant solution and thermally activated peroxy acids as free radicals for efficient pollutant degradation. Here, a brand-new technique for degrading organic pollutants with a "Win-Win-Win" concept was purposed for lignocellulose valorization, pollutant control by waste tail-gas, and biofuel production.

Insights into lignocellulosic waste fractionation for lignin nanospheres fabrication using acidic/alkaline deep eutectic solvents.

Facile fractionation of lignocellulosic waste into useable forms is essential to achieve a multi-product treatment process especially when the resulting lignin streams are expected for high-value materials valorization. Despite acidic/alkaline deep eutectic solvents (DESs) are promising solvents for lignocellulosic waste fractionation, there is little information about their differences in the fractionation and lignin extraction profiles. In this work, four DESs that were cataloged to acidic types (formic acid-choline chloride, lactic acid-choline chloride) and alkaline types (monoethanolamine-choline chloride, glycerol-K2CO3) were investigated to compare their abilities of bamboo waste fractionation. Physicochemical properties of these resulting cellulose, lignin and derived lignin nanospheres (LNPs) were also assessed. Results showed that DESs could selectively extract lignin via cleaving lignin-carbohydrate linkages and lignin ether bonds. Acidic DESs pretreatments were more effective in biomass delignification (~95.0 %), while alkaline DESs showed better polysaccharide retention. Glycerol-K2CO3 LNPs exhibited much smaller sphere size (50-100 nm) while acidic DESs LNPs showed higher thermal stability due to higher extent of lignin condensation. In addition, MEA-ChCl could introduce amine groups onto lignin hydroxyl. This work provided insightful information for tailoring technique routes to selective lignocellulosic waste fractionation, while facilitating the downstream applications of the obtained cellulose/lignin.

Synthesis of cellulose II-based spherical nanoparticle microcluster adsorbent for removal of toxic hexavalent chromium.

Since natural cellulose is mostly cellulose I and has a fibrous form, most cellulose-based adsorbents are fibrous/rod-shaped and exhibit the cellulose I crystal structure. This study reports a cellulose II-based spherical nanoparticle microcluster adsorbent (SNMA), synthesized from biomass by a bottom-up approach, for removing toxic hexavalent chromium (Cr(VI)). The basic structure of SNMA was investigated. Notably, the prepared adsorbent was a microcluster composed of spherical nanoparticles, while exhibiting cellulose II crystal structure, resulting in higher thermal stability and significantly enhanced adsorption performance. The adsorption process and mechanism of SNMA on Cr(VI) were studied in detail. The SNMA achieved a high adsorption capacity (225.94 mg/g) and receptor site density. The SNMA is expected to be used as a bio-based spherical nanoparticle microcluster adsorbent platform for the adsorption of different toxic substances by changing the surface functional groups of its components, spherical nanoparticles.

Bacterial cellulose/lignin nanoparticles composite films with retarded biodegradability.

In practical applications, the full biodegradability of all-biomass-based bacterial cellulose (BC) composites enhances their environmentally friendliness but results in the poor durability especially at humid conditions. This work prepared BC/lignin nanoparticles (LNPs) composite films with retarded biodegradability, which could broaden their application area. Three LNPs were fabricated using technical lignins extracted by deep eutectic solvent (DES), ethanol organosolv, soda/anthraquinone from poplar. LNPs involvement during BC fermentation showed limited influence on its productivity but significantly retarded the biodegradation of composite films. The potential inhibition mechanism was physical barrier and non-productive binding of LNPs. The BC/Soda LNPs showed much higher retarded degradation property (~58 wt% degradation) compared to BC/Organosolv LNPs and BC/DES LNPs (~85 wt% and ~ 97 wt% degradation respectively) at high enzyme loadings of 5 mg g-1 BCE. While at low enzyme loadings of 1 mg g-1 BCE, all these three composite films showed comparable retarded degradation property of ~60 wt%.

Why can hydrothermally pretreating lignocellulose in low severities improve anaerobic digestion performances?

A lignocellulosic residue, rice straw, was hydrothermally pretreated for the whole slurry anaerobic digestion. In contrast to the unpretreated rice straw, 110-120 °C pretreatment promoted biogas yield by 35%-38%, while only 14% promotion happened on the pretreatment at 180 °C. To understand why this improvement happened at lower severities, the pretreated rice straw at 90 °C, 120 °C, and 180 °C were selected for the further investigation, in which the liquor and solid fraction were separated for digestion, and compared with the whole slurry digestion. Results indicated more methane was released from the derived liquor of 180 °C than that of 90 °C and 120 °C, however, solid fraction did not exhibit significantly different methane yields (187.77-193.91 mL/g TS). These results suggested that the released soluble fraction from pretreatment could facilitate the methanogenesis. Furthermore, the released inherent soluble fraction in rice straw was mainly responsible for higher biogas yield at lower temperatures. Pretreatment at higher temperatures disintegrated the rice straw recalcitrance more, and intensified the release of soluble fraction accordingly. Consequently, the methanogenesis of whole slurry could be promoted at the initial digestion; the hydrolysis/acidification of the solid fraction in whole slurry was weakened greatly, which resulted in a lower biogas yield. This can also be proved by the evolution of dominant bacteria and archaea in the anaerobic digestion of whole slurry, separated solid and liquor fraction.

3-D hierarchical porous carbon from oxidized lignin by one-step activation for high-performance supercapacitor.

To convert lignin into high-valued carbon materials and understand the lignin structure function, oxidized lignin, a by-product from lignocellulose PHP-pretreatment (phosphoric acid plus hydrogen peroxide), was carbonized by one-step KOH-activation; the physico-chemical characteristics and electrochemical performances of the harvested carbons were also investigated. Results indicated the resultant carbons displayed 3-dimensional hierarchical porous morphology with maximum specific surface area of 3094 m2 g-1 and pore volume of 1.72 cm3 g-1 using 3:1 KOH/lignin ratio for carbonization. Three-electrode determination achieved a specific capacitance of 352.9 F g-1 at a current of 0.5 A g-1, suggesting a superior rate performance of this carbon. Two-electrode determination obtained an excellent energy density of 9.5 W h kg-1 at power density of 25.0 W kg-1. Moreover, 5000 cycles of charge/discharge reached 88.46% retention at 5 A g-1, implying an outstanding cycle stability. Basically, low molecular weight and abundant oxygen-containing functional groups of employed lignin mainly related to the excellent porous morphology and the outstanding electrochemical performances, suggesting the oxidized lignin was an ideal precursor to facilely prepare activated carbon for high-performance supercapacitor. Overall, this work provides a new path to valorize lignin by-product derived from oxidative pretreatment techniques, which can further promote the integrality of lignocellulose biorefinery.

Mechanistic insight into different adsorption of norfloxacin on microplastics in simulated natural water and real surface water.

Microplastics (MPs) as carriers of various contaminants have attracted more attentions in water environments. However, the interactions between typical MPs and norfloxacin (NOR) in natural water environments were still not systematically studied. In this study, the adsorption of NOR onto four typical types of MPs (polyethylene (PE), polypropylene (PP), polystyrene (PS), and polyvinyl chloride (PVC)) was investigated in simulated natural water and real surface water, and the adsorption mechanisms were deeply explored to provide fundamental understandings of the MPs-NOR complicated pollution. The results showed that the kinetics of NOR onto all MPs obeyed pseudo-second-order model, and was greatly slowed down at lower temperature or higher salinity. The intrinsic structure and surface area of MPs played important roles in the adsorption behaviors of NOR on these four types of MPs. The adsorption isotherm of NOR onto all MPs could be well described by linear model, with the Kd values following the order of PVC > PS > PE > PP (i.e. 6.229-11.901 L/µg) in simulated natural water. However, in surface water the adsorption isotherms of NOR on all MPs could be well fitted by Freundlich model. For all MPs, the adsorption of NOR was quite pH-dependent due to the electrostatic interactions. Furthermore, the salinity and the presence of dissolved organic matter (DOM) had significantly hindered the NOR adsorption. More importantly, compared with adsorption behaviors in simulated natural water, the competition of coexisting substances such as cations and NOM for adsorption sites and higher water pH dramatically reduced the adsorption of NOR onto all types of MPs in Jiang'an River, with the reduction rate of 19.7-41.2%. Finally, the mechanism studies indicated that the electrostatic attractions played a key role in the adsorption of NOR onto MPs, and π-π, H-bonding, polar-polar, and Van Der Waals interactions were also involved in adsorption processes.

Spherical center and rotating platform hinged knee prosthesis: Finite-element model establishment, verification and contact analysis.

BACKGROUND: Biomechanical study is fundamental for the preclinical evaluation of knee prostheses. However, there are few reports on the contact characteristic investigation in the hinged knee prosthesis. The purpose of this study was to investigate the contact characteristics of a novel hinged knee prosthesis. METHODS: All of the component models were designed and assembled using Solidworks. A comparison of the contact area and ultra-high-molecular-weight polyethylene (UHMWPE) deformation using the experimental method (EM) and finite-element analysis (FEA) under 3000 N with the prosthesis at different flexions was performed. The peak contact pressure and von Mises stress on tibial insert and bushing were investigated under nine specific samples that were extracted from a gait cycle using FEA (according to ISO 14243-1: 2009). RESULTS: The largest contact area and UHMWPE deformation were 100.78 ± 8.71 mm2 and 0.085 ± 0.015 mm in the EM, and 96.68 mm2 and 0.096 mm in FEA. The peak contact pressure and von Mises stress on the tibial insert were 26.3071 MPa and 10.5115 MPa at 13% of the gait cycle and on bushing were consistently 0 MPa. The contact pressures were distributed at the posterior of the insert. CONCLUSION: The finite-element model was validated to be applicable for predicting the real prosthesis behavior based on the good correlation of the results using the EM and FEA. The model can help to identify contact characteristics and be can used in optimization studies of this novel prosthesis during the design phase.

Evaluation of Hydrothermal Pretreatment on Lignocellulose-Based Waste Furniture Boards for Enzymatic Hydrolysis.

Three typical waste furniture boards, including fiberboard, chipboard, and blockboard, were pretreated with conventional hydrothermal method. The responses of chemical composition, physicochemical morphology, and performances of enzymatic hydrolysis were evaluated. Results indicated the almost complete hemicellulose removal at higher pretreatment temperatures, the enhanced crystallinity index, and disordered morphology of the pretreated substrates indicated that the hydrothermal pretreatment deconstructed these boards well. However, the very low enzymatic hydrolysis (< 8% after 72 h) of the pretreated substrates showed the poor biological conversion. Three hypotheses for the weakened enzymatic hydrolysis were investigated, and results indicated that the residual adhesives and their degraded fractions were mainly responsible for poor hydrolysis. When NaOH post-pretreatment was attempted, cellulose-glucose conversion of the hydrothermally pretreated fiberboard, chipboard and blockboard can be improved to 28.5%, 24.1%, and 37.5%. Herein, the process of NaOH hydrothermal pretreatment was integrated, by which the hydrolysis of pretreated fiberboard, chipboard and blockboard was greatly promoted to 47.1%, 37.3%, and 53.8%, suggesting a possible way to pretreat these unconventional recalcitrant biomasses.

Acidic deep eutectic solvents pretreatment for selective lignocellulosic biomass fractionation with enhanced cellulose reactivity.

This work tailored a promising two-step pretreatment, i.e., liquid hot water extraction followed by mild acidic deep eutectic solvents pretreatment for clean lignocellulose fractionation while enhancing cellulose reactivity for its subsequent utilization. The abilities of three acidic deep eutectic solvents (formic acid-, acetic acid- and lactic acid-choline chloride) to selectively extract poplar wood lignin and enhance cellulose reactivity were comparatively assessed. Results showed that rather high lignin selectivity of 6.3-7.9 was obtained while the available area and porosity of the resulting cellulose were significantly increased. The resulting cellulose pulps exhibited comparable chemical reactivity to commercial bleached Kraft pulp when cellulose acetate was selected as testing cellulose derivative for demonstrating purpose, showing their great promise for high-value use. It was proposed that the unique ionic properties of these acidic deep eutectic solvents were responsible for their selective lignin removal and cellulose swelling/deconstruction to enhance cellulose chemical reactivity.