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Phase change materials (PCMs) are promising for thermal energy storage due to their high latent enthalpy and constant phase change temperature. However, organic PCMs suffer from leaking, low thermal conductivity, and flammability. Herein, high thermal conductivity, photothermal and flame-proof docosane microcapsules with melamine-formaldehyde (MF) and polypyrrole (PPy) (C 22 -CMFP) were reported with cellulose nanocrystal (CNC) stabilized Pickering emulsion droplets as templates through in-situ polymerization. CNCs showed outstanding C 22 Pickering emulsifying ability with the presence of NaCl and provided ideal templates for C 22 microcapsules. The obtained C 22 -CMFP microcapsules displayed high enthalpy (205.7 J/g), C 22 core ratio (86.1 %), and stability. The C 22 -CMFP microcapsules retained an outstanding enthalpy remaining ratio (98.9 %) after 100 times cooling/heating cycles and could tolerate 100 °C for 12 h without leaking due to the robust hybrid CMFP shell. PPy significantly improved the thermal conductivity and photothermal conversion efficiency of C 22 -CMFP microcapsules. The C 22 -CMFP microcapsules exhibited a high thermal conductivity of 0.683 W/(m·K). The maximum temperature of C 22 -CMFP microcapsules under light irradiation for 18 min was 60.4 °C. Moreover, C 22 -CMFP microcapsules showed superb flame-proof properties. This study provides a facile approach to fabricate high enthalpy, stable, thermal conductive, photothermal, and flame-proof PCM microcapsules for solar harvesting and thermal energy storage., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier B.V.)

As the second most abundant polysaccharide on earth, chitin-based films are promising packaging and biomedical materials. However, the lack of special function (especially UV-blocking properties and fluorescence) usually restricts their further and high-value applications. Herein, high UV-blocking and fluorescence chitin-based films were fabricated via surface modification using acetoacetation and the Hantzsch reaction. The structure and properties of the films were characterized by NMR, FTIR, fluorescence spectrum, and tensile tests. The results showed that the benzene ring and 1,4-dihydropyridine ring (DHP) were successfully grafted on the films in the mild process. Besides, the degree of substitution of DHP (DS DHP ) increased with the reaction time, temperature, and substrate concentration. Moreover, the modification followed a first-order reaction at 20 °C with a rate constant of 2.1 × 10 -4 . When the DS DHP was over 0.029, the films exhibited 100 % UV shielding. The fluorescence spectrum demonstrated that the films had excellent solvent and temperature resistance. In addition, the films exhibited excellent mechanical strength with tensile strength up to 85.2 MPa. This work provides a facile and environmentally friendly strategy to fabricate a functional chitin-based film with potential applications in UV protection, medical packaging, and fluorescent materials., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier B.V.)

This study aimed to explore the synergistic mechanism of lignin chromophore modifications via UV treatment and to analyze the effects of mechanical treatments on LCNF properties for future uses. The procedure involved two steps: first, lignin's chromophore modification via UV illumination, and then the ball milling process was proceeded for 1 h, followed by high-intensity ultrasonic for 15-135 min. Characterization included preserved lignin content percentage, FTIR, UV-vis NMR, and color analysis for UV-modified samples, and to access the influence of mechanical treatment on LCNF samples further yield, zeta potential analysis, XRD, thermogravimetric analysis, atomic force microscopy, and scanning electron microscopy were performed. LCNFs S-120 demonstrated a zeta potential of -21.7 mV, indicating enhanced stability compared to the S-135 sample (-10.95 mV). The S-120 sample also showed the highest yield (74.02 %) and TGA at 391 °C. In XRD analysis, the S-120 sample demonstrated the highest CrI 64.3 %, than the S-15 sample (48.2 %). Preserved lignin in the LCNFs led to a slight reduction in crystallinity across all samples but improved thermal stability for all the prepared LCNFs samples. The UV and ultrasonication improved the homogeneity and durability of the LCNF samples, enabling a process that may be used to industries., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Cellulose paper is a flammable and hygroscopic material, which limits its application. In this paper, melamine-formaldehyde resin (MF) and silane coupling agents were used to microencapsulate ammonium polyphosphate (Si@MFAPP) in turn and added to the fibers suspension to prepare hydrophobic and flame-retardant cellulose paper. It was found that the surface of the ammonium polyphosphate (APP) was smooth with the water solubility of 0.24 g/100 mL. After microencapsulation with MF, the surface of MFAPP became rough, and the solubility was reduced to 0.1 g/100 mL. When further encapsulation with polysiloxanes, the surface showed significantly higher roughness, and a lotus leaf-like microspherical structure was formed. Specifically, its solubility decreased to 0.04 g/100 mL. In addition, the residual char weight of Si@MFAPP at 800 °C was increased from 25.27 % to 38.56 %. The water contact angle (WCA) of MFAPP/Pulp increased from 84.23° to 90.78°, and the limiting oxygen index (LOI) increased from 31.8 % to 34.1 %, meaning that the flame retardancy was obviously raised. The WCA of Si@MFAPP/Pulp enhanced to 96.45°, and the LOI was 34.5 %, meaning that the hydrophobicity was further raised. Therefore, Si@MFAPP significantly improved the flame-retardancy and hydrophobicity of the cellulose paper., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

This study explored the synthesis of lignin-polyol (LP) by liquefaction of Kraft lignin in polyethylene glycol and glycerol. LP23 (23 wt% lignin) and LP41 (41 wt% lignin) were obtained with remarkable liquefaction yields of 97.43 % and 93.75 %, respectively. LP-based polyurethane film (LP-PUF) was then fabricated by reacting LP23 and LP41 with hexamethylene diisocyanate. Mechanical properties and hydrophobicity of LP-PUF were optimized by varying NCO/OH molar ratios. LP23-PUF1.9 with NCO/OH of 1.9 showed excellent tensile strength of 34.28 MPa and Young's modulus of 233.27 MPa, while LP41-PUF2.0 with NCO/OH of 2.0 exhibited good tensile strength of 26.03 MPa and Young's modulus of 260.66 MPa. LP23-PUF2.0 displayed high hydrophobicity as indicated by the water contact angle of 96.8° and low surface free energy of 15.68 mN/m. Glass transition temperature (Tg) of LP-PUF varied depending on lignin content and NCO/OH molar ratio. Specifically, the increase of KL content from 23 % to 42 % induced big rise of Tg by 8 °C. The NCO/OH induced change of Tg was relatively weak, as indicated by the small increase of -2.71 °C of LP41-PU1.4 to -1.81 °C of LP41-PUF2.0. The results of this work offer insights for lignin utilization as structural component of high modulus and high strength polyurethane film., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Black liquor, primarily consisting of lignin, polysaccharides, and inorganic substances, is a potential precursor of porous carbon materials for high-performance supercapacitors. However, the laborious purification of black liquor lignin and the introduction of exogenous heteroatoms have hindered their practical applications. Herein, the full components of black liquor were utilized to synthesize hierarchical porous sulfur self-doped lignin carbons (S-LCs) through a self-activation process aimed at improving the performance of supercapacitors. Benefiting from the intensified reactivity and crosslinking degree of the polysaccharide component and the sulfur self-doping and self-activation effect of inorganic substances, the resulting S-LCs exhibit a high specific surface area (SSA), abundant porous structure, and enhanced defect activity, all contributing toward increasing the energy storage capacity of supercapacitors. The as-obtained S-LC-G250/700 features a high SSA of 892.94 m 2  g -1 and a sulfur content of 3.3 at.%. The S-LC-G250/700 demonstrates excellent specific capacitance (e.g., 405.06 F g -1 at 0.5 A g -1 ), remarkable stability (103 % capacity retention after 10,000 cycles), and high energy density of 30.4 Wh kg -1 . Density functional theory calculations verified the advantages of the high-content sulfur self-doping of black liquor, suggesting that self-doped sulfur contributes to charge adsorption on porous carbon surfaces and promotes electron transfer in the electrolyte., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier B.V.)

Algal enzymes are essential catalysts in numerous biological reactions and industrial processes owing to their adaptability and potency. The marketing of algal enzymes has recently risen due to various reasons, including the cost-efficient manner of their cultivation in photobioreactors, the eco-friendly production of high biomass contents, sources of novel enzymes that used in many sectors (biofuel and bioremediation applications), sustainability, and more renewability. Oxidoreductases and hydrolytic enzymes are among the important applied algal enzymes in industrial applications, with annually growing demand. These algal enzymes have opened up new avenues for significant health advantages in reducing and treating oxidative stress, cardiovascular illness, tumors, microbial infections, and viral outbreaks. Despite their promising uses, commercial applications of algal enzymes face many difficulties, such as stability, toxicity, and lower data availability on specific and adequate catalytic mechanisms. Therefore, this review focuses on the algal enzyme types, their uses and advantages over other microbial enzymes, downstream and upstream processing, their commercial and marketing, and their challenges. With the constant development of novel enzymes and their uses, enzyme technology provides exciting options for several industrial sectors., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Cellulose-based aerogels have emerged as highly promising materials for oil-water separation because of their highly porous nature, low bulk density, cost-effectiveness, and functional performance. In this study, a novel, robust, and hydrophobic bacterial cellulose aerogel (HBCA) was reported for highly efficient oil/water separation, which was formed by incorporating methyltrimethoxysilane (MTMS) into sulfonated nano-fibrillated bacterial cellulose (SNBC) matrix through freeze-drying method. The structural integrity of the SNBC/MTMS aerogel was ensured by its three-dimensional linked network structure. The resultant aerogel demonstrated superior hydrophobicity with a contact angle of 152.4°. As an oil-absorbing material, it selectively adsorbed different types of oils and organic solvents, with a saturation adsorption capacity ranging from 42.14 to 85.37 g·g -1 . Additionally, this composite aerogel demonstrated outstanding separation efficiency (98.48 %) in continuous oil-water mixture processes, suggesting promising potential applications in the treatment of industrial oil pollution and oil spill accidents. This study indicates that the proposed HBCA with sulfonated nano-fibrillated bacterial cellulose is a potential and effective material for addressing environmental challenges related to oil contamination., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Natural laccases are a family of multi‑copper oxidases that can oxidize multiple phenol substrates and of great importance to contaminant remediation and biosensing. However, the construction of substitutes for the expensive and perishable laccase used in harsh conditions remains a great challenge. Here, we reported a novel strategy for the fabrication of copper-doped lignin-based laccase nanozymes (Cu-AL) through the coordination of aminated lignin and different copper sources. The Cu-AL prepared from CuSO 4 , possessed highest Cu content and Cu + proportion, exhibited the best laccase-like activity to various phenols degradation. Strikingly, the thermophilic Cu-AL exhibited superior catalytic activity at 100 °C (3.23 times than that of 60 °C) and durability (> 50 % activity even after 160 days stored in water). Furthermore, a smartphone-based detection platform was successfully developed to achieve the rapid, convenient, and accurate detection of epinephrine concentration. In summary, this work provides a new sustainable and low-cost way to design robust laccase nanozymes from lignocellulose biomass, especially for expanding the applications of enzymatic reaction with high-temperature operation and/or long-term storage in environmental remediation and biosensing., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

The goal of the current work is to showcase the synthesis of homogeneous pullulan nanofibers that are strengthened by the addition of cellulose nanofibrils (CNF). One of the main difficulties this study faced was determining the ideal water/organic solvent ratio for the electrospinning process, which would allow for the maximum reduction in the amount of organic solvent (DMF or DMSO) needed. The rheological behavior of electrospinning solutions was modulated by varying both, the pullulan concentration and solvent system composition. The amount of CNF in the composition significantly affects the properties of the created nanofibers. When the CNF content increased from 1 % to 5 %, the diameter of the fibers decreases from 284 nm to 90 nm. This is attributed to the enhanced conductivity and surface charge density of the solution jet. The as prepared nanofibres can hold a variety of drugs and can be used to create novel formulations for various biomedical purposes. The nanofibres were tested for salicylic acid incorporation and release. Drug release exhibited zero-order kinetics, suggesting that the concentration remained unaffected by the rate of release. Furthermore, the nanofibres demonstrated remarkable antibacterial activity against both Gram-positive and Gram-negative bacteria., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier B.V.)

Hydrogels used for flexible sensing usually require a good balance between mechanical strength and conductivity. In this study, polyvinyl alcohol/carboxymethyl cellulose/cellulose nanofibers (PVA/CMC/CNF) hydrogels with multi-hierarchical structures were firstly prepared by adjusting the CNF content. Then, PVA/CMC/CNF-xM with excellent mechanical properties and conductivity were prepared by cyclic freezing-thawing and sodium citrate/aluminium chloride (Na 3 Cit/AlCl 3 ) dual ions salt equilibrium methods. Results showed that at an ion concentration of 3 mol/L, PVA/CMC/CNF-3 M hydrogel exhibited a tensile strength, elongation at break and conductivity of 3.41 MPa, 1271 % and 0.35 S/m, respectively. The structural evolution of PVA/CMC/CNF-xM conductive hydrogels were studied, and the results indicated that Cit 3- formed numerous intermolecular hydrogen bonds, while Al 3+ could strongly coordinate with carboxyl and hydroxyl groups between the polysaccharide chains. Meanwhile, PVA/CMC/CNF-3 M possessed a low strain detection limit of 1 %, making it not only can be used for human motion monitoring, but also information encoding and transmission. This work may provide a facile approach for preparing high-strength and conductive hydrogels, which can be applied in flexible wearable electronic devices and information transmission., Competing Interests: Declaration of competing interest The authors declare that they have no conflicts of interest., (Copyright © 2024 Elsevier B.V. All rights reserved.)

A facile green hydrothermal method was developed for the preparation of fluorescent carbon dots (CDs) using sugarcane bagasse (SB) as a raw material. The incorporation of CDs within the hydroxyethyl cellulose-acrylamide hydrogel (HEC-AM) in the presence of glutardehyde (GA) as a crosslinking agent showed bright red emission under fluorescence microscope. The hydroxyethyl cellulose-N-CDs-acrylamide hydrogel (HEC-AM@N-CDs) were used as alternative biocompatible fluorescent probes for imaging and suppression of Gram-negative bacteria such as Escherichia coli (with inhibition zones 13 mm for HEC-AM to 17 mm for HEC-AM@N-CDs) & Helicobacter pylori (with inhibition zones 16 mm for HEC-AM to 13 mm for HEC-AM@N-CDs) and Gram-positive bacteria such as Micrococcus luteus (with inhibition zones 15 mm for HEC-AM to 16 mm for HEC-AM@N-CDs) & Staphylococcus aureus (with inhibition zones 13 mm for HEC-AM to 14 mm for HEC-AM@N-CDs). The N-CDs promote bacterial binding and internalization, leading to differential fluorescence emission depending on the bacteria's cell wall composition. DFT calculations support strong interactions between the bacteria and HEC-AM@N-CDs., Competing Interests: Declaration of competing interest The authors declare no competing interests., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Foam materials possess notable features, including low density, high porosity, low thermal conductivity, and high impact resistance, making them extensively used in various sectors such as construction, transportation, water treatment, and packaging. However, the majority of commercial foam materials are derived from synthetic polymers based on fossil fuels, which raises concerns regarding health and ecology. In this work, we present a straightforward and scalable approach (physical cross-linking and common pressure drying) for fabricating a bio-based foam material using pulp fibers sourced from discarded sugarcane bagasse and sodium alginate extracted from seaweed. The resulting foam material exhibits low density (13.7-20.5 kg/m 3 ), exceptional thermal insulation properties (thermal conductivity as low as 38.6 mW/mK), thermal stability (no deformation at 140 °C), and mechanical strength. After a basic silane modification, it also shows favorable water resistance (with a contact angle of 128°). Moreover, the foam material demonstrates remarkable degradation performance, with a degradation rate exceeding 93.8 % after 90 days of burial in soil. Therefore, this novel method offers a sustainable solution for eco-friendly foam production across various application domains., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier B.V.)

Cellulose material is emerging as a promising alternative to polyolefin separators in lithium-ion batteries (LIBs) due to its wide availability, electrolyte wettability and thermal stability. Based on the non-solvent induced phase separation, dissolving and regenerating the cellulose material by environmentally friendly solvents and non-solvent enables the efficient and pollution-free preparation of porous regenerated cellulose separator (RCS), greatly expanding their application potential in LIBs. However, the mechanical strength of pure RCS still hardly satisfactory, due to the weak intermolecular bonding and loose porous structure. Therefore, this study introduced an acrylic acid/acrylamide (AA/AM) polymer cross-linking system forming an interpenetrating network with the cellulose framework to produce a double network regenerated cellulose separator (DN-RCS) with high mechanical strength and high porosity. At meantime, the special functional group on AA/AM can influence the transport process of Li + and PF 6 - in the electrolyte, helping to form a stable interface on the electrolyte/lithium anode surface to reduce the formation of lithium dendrites. The results showed that DN-RCS possessed excellent mechanical strength and porosity compared to RCS. The high ionic conductivity of DN-RCS (1.03 mS cm -1 ) enabled the assembled cell with excellent cycling stability (90.8 % at 0.5C for 100 cycles) and rate performance (65.2 % at 5C). This work provides a further feasible strategy for the preparation of a high-performance cellulose-based separator., Competing Interests: Declaration of competing interest There are no conflicts of interest to declare in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Kinsenoside is a rare and valuable glycoside with extensive bioactivities. However, the enzymatic synthesis of kinsenoside has been a challenging task due to the limited enzyme toolbox and unsatisfactory yield. Herein, the β-glucosidase from Dictyoglomus thermophilum (DtBGL) was heterologously expressed, purified and enzymatically characterized. The purified DtBGL was successfully immobilized on the metal-organic frameworks of UiO-66-NH 2 . The DtBGL@UiO-66-NH 2 was fully characterized using SEM, XRD, TGA and FTIR. The studies on enzymatic properties demonstrated that DtBGL@UiO-66-NH 2 exhibited increased catalytic activity and stability compared to the free DtBGL. Particularly, DtBGL@UiO-66-NH 2 could catalyze the synthesis of kinsenoside via the reverse hydrolysis reaction and the kinsenoside yield was 34.12 % under the optimized catalytic system, which was 1.9-fold higher compared with the free DtBGL. Moreover, DtBGL@UiO-66-NH 2 displayed good reusability with a kinsenoside yield of 27.02 % after reuse for 3 times. The present work not only identifies and characterizes a highly active β-glucosidase with reverse hydrolysis activity, but also proposes the immobilized enzyme as an effective catalyst for the industrial production of glycosides., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Cellulose nanofibrils (CNFs) can serve as an efficient surface enhanced Raman scattering (SERS) platform for in situ detection of trace targets. In this study, a highly reproducible SERS platform based on TEMPO-oxidized CNFs (T-CNFs) was fabricated by the ion-exchange. Self-assembly of silver nanoparticles (AgNPs) was accomplished in only 120 s. The abundant carboxylate groups and good hydrophilicity of T-CNFs facilitated uniform and dense loading of AgNPs over the surface area. The obtained SERS substrate greatly enhanced the Raman signal of different pesticides, and the detection limits of thiram and thiabendazole were 5.81 × 10 -8  M and 9.63 × 10 -8  M, respectively. SERS substrate could produce homogeneous Raman-enhanced signals (relative standard deviation (RSD) = 6.59 %). In addition, due to the good flexibility, SERS substrate could collect and detect pesticide residues from the surface of apples. The intensities of Raman characteristic peak at 1384 cm -1 showed a good linear relationship with the analyte concentrations (0.96 ng/cm 2 -9600 ng/cm 2 ). The constructed SERS substrate provided a theoretical basis for the preliminary rapid screening of hazardous chemical residues in food, which was of great value for the SERS technique to become a routine on-site analysis method for pesticide residues., Competing Interests: Declaration of competing interest The authors state that there are no conflicts of interest to disclose., (Copyright © 2024 Elsevier B.V. All rights reserved.)

As an emerging non-wood resource, moso bamboo has attracted extensive attention because of its short growth cycle and high holocellulose content. However, the internal structure of moso bamboo is more compact than that of wood, leading to higher chemical consumption during the pulping process, which greatly reduces the quality of the extracted fibers. Herein, an innovative pulping system including enzymes and alkali is proposed to achieve higher-quality extraction of moso bamboo fibers. Benefiting from the synergistic effects of high-temperature and alkali-resistant cellulase, xylanase, and laccase, supplemented with alkaline pulping, adequate retention and softening of moso bamboo fibers were ultimately achieved. The sample treated with an enzyme/alkali system resulted in a relative increase in fiber length of 7.19 % and a 31.26 % increase in beating efficiency over alkaline pulping. In addition, the tensile index and tearing index of the paper treated with the enzyme/alkali system reached 50.17 N·m·g -1 and 9.12 mN·m 2 ·g -1 , which were 22.52 % and 20.53 % higher than those of the alkaline pulping, respectively. This work provides new insights into the production of high-performance moso bamboo fibers and paper with low energy and alkali consumption., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier B.V.)

Developing sustainable matrix and efficient bonding mode for preparing room temperature phosphorescence (RTP) materials with full-color afterglows is attractive but still challenging. Here, xylan, a hemicellulose by-product from the paper mill, is used to construct full-color RTP materials based on imine bonds. Xylan is oxidation by periodate to introduce aldehyde groups to increase reaction sites; aromatic amines with different π conjugations can be readily anchored to dialdehyde xylan (DAX) by imine chemistry. The dual rigid environments were constructed by hydrogen bonding and imine covalent bonding, which can facilitate the triplet population and suppress non-radiative transitions, thus the xylan derivatives display satisfactory RTP performances. As the degree of conjugation of the chromophore increases, the afterglow colors can be changed from blue to green, yellow, and then to red. Thus, such a universal, facile, and eco-friendly strategy can be used to fabricate full-color RTP materials, which show a bright future in information encryption and advanced anti-counterfeiting. These results unambiguously state that the biodegradable paper mill waste-based RTP materials are convincingly expected to replace and surpass petroleum polymer-based counterparts., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Food safety and wastage caused by fruit deterioration is a serious global problem. Effective packaging systems for extending the freshness period of fruit play a key role in food safety. In this work, we constructed an eco-friendly and flexible polysaccharide-based packaging film based on hydroxypropyl guar (HPG), cellulose nanocrystals (CNCs), deep eutectic solvents (DES) and anthocyanin (Anth). DES could endow polysaccharide films with multiple hydrogen bond numbers and good stability. Hydroxypropyl guar/cellulose nanocrystals/anthocyanin with 0.2 g deep eutectic solvents (HCA-DES 0.2 ) had good tensile properties, oxygen barrier properties (3.01 cm 3 /m 2 ·day·Pa), water resistance (WCA 111.97°), antibacterial (CFU ˂ 10 3 ), and transparency (55.4 %). The preservation tests of grape and blueberry showed that the shelf life of these two fruits was 12-20 days, and the polysaccharide film had great application potential in fruit preservation., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

In a quest to find eco-friendly materials from renewable resources, researchers have focused on cellulose materials, which is the primary reinforcing component of plant cell walls. Nanocellulose is at the forefront of research due to its wide range of sources, biocompatibility, large surface area and tunable surface chemistry. It has gained considerable attention in various industries as a nano-reinforcement for polymer matrices due to its hierarchical structure (medical and healthcare, oil and gas, packaging, paper, board, composites, printed and flexible electronics, 3D printing, aerogels). In this paper, we have reviewed the recent advances in nanocellulose production, physical properties, structural characterization, surface modification strategies, pretreatment methods, applications, limitations and future directions. This review emphasizes the quantification of nanocellulose extraction and applications of the most prevalent areas of nanocellulose research. In view of its increasing and broader applications, the demand for nanocellulose is expected to increase in the future., Competing Interests: Declaration of competing interest The authors declare no conflict of interest., (Copyright © 2024 Elsevier B.V. All rights reserved.)

This research introduces a novel upcycling method for transforming cigarette filters-an abundant and persistent environmental waste-into high-performance epoxy composites reinforced with cellulose nanofibers. The innovation lies in extracting cellulose acetate nanofibers from used cigarette butts via a multi-step purification and electrospinning process, followed by their conversion into regenerated cellulose nanofibers through alkaline hydrolysis. This dual-fiber approach allows us to fabricate four distinct epoxy composites, each reinforced by different nanofiber types: recycled cellulose acetate nanofibers, regenerated cellulose nanofibers from recycled cigarette filters, and their commercial counterparts. Notably, this is the first time regenerated nanofibers derived from waste cigarette filters have been utilized for epoxy composite reinforcement, demonstrating a sustainable, high-value use for a major pollutant. Comprehensive characterizations, including FTIR, XRD, SEM, and contact angle measurements, confirmed the successful regeneration of cellulose nanofibers, showing improved hydrophilicity, reduced crystallinity, and uniform nanofiber morphology with diameters between 200 and 300 nm. The innovation further extends to the mechanical performance of these composites: tensile tests revealed that those reinforced with regenerated cellulose nanofibers exhibited superior tensile strength (49.5-53.8 MPa), significantly outperforming both cellulose acetate nanofiber composites (40.1-42.6 MPa) and neat epoxy resin (31.4 MPa). This marked improvement is attributed to enhanced nanofiber dispersion and interfacial adhesion within the epoxy matrix, an essential advancement over traditional composites. In addition, thermal analysis showed that all composites maintained thermal stability in the 300-400 °C range, comparable to commercial alternatives. The regenerated nanofiber-reinforced composites also displayed enhanced optical transparency due to reduced light scattering, making them ideal candidates for applications requiring both mechanical strength and optical clarity. By pioneering the use of cigarette filter waste for fabricating advanced cellulose nanofiber composites, this study presents an eco-friendly approach to addressing environmental pollution while creating sustainable materials with superior mechanical, thermal, and optical properties., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

The increasing interest in lignin, a complex and abundant biopolymer, stems from its ability to produce environmentally beneficial biobased products. β-Etherases play a crucial role by breaking down the β-aryl ether bonds in lignin. This comprehensive review covers the latest advancements in β-etherase-mediated lignin valorization, focusing on substrate selectivity, enzymatic oxidative activity, and engineering methods. Research on the microbial origin, protein modification, and molecular structure determination of β-etherases has improved our understanding of their effectiveness. Furthermore, the use of these enzymes in biorefinery processes is promising for enhancing lignin breakdown and creating more valuable products. The review also discusses the challenges and future potential of β-etherases in advancing lignin valorization for biorefinery applications that are economically viable and environmentally sustainable., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Lignocellulosic papers (LCP) are favored for electrical insulating applications due to their environmental friendliness, ease of processing, and cost-effectiveness. However, the loose structure and numerous pores inside LCP result in the poor mechanical and electrical insulating properties, posing challenges in meeting the requirements for the rapid upgrading of high-voltage electrical equipment. Herein, a 3D interconnective structure composed of 3D aramid nanofibers (ANF) and 2D carbonylated basalt nanosheets (CBSNs) is introduced to enhance the structure and the chemical bonding interactions of LCP. This is achieved by impregnating LCP into an ANF-CBSNs suspension, where the 3D interconnective ANF framework hosts numerous CBSNs. The resultant LCP/ANF-CBSNs (LCP/A-C) composite papers exhibit multilayered structure and multiple hydrogen-bonding interactions, demonstrating excellent mechanical and electrical insulating properties. Notably, the optimized LCP/A-C5 composite papers exhibit remarkable tensile strength (23.15 MPa) and dielectric breakdown strength (20.14 kV·mm -1 ), respectively, representing 229 % and 145 % increase compared to those of the control LCP. These impressive properties are integrated with excellent bending ability, outstanding high temperature resistance, exceptional volume resistivity, and low dielectric constant and loss, demonstrating their potential as highly promising electrical insulating papers for advanced high-power electrical equipment., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Wheat straw, as a non-wood fiber waste, is available worldwide and can be used in cellulosic matric production, promoting the application of sustainable materials. However, poor fiber properties and water drainage are the primary obstacles to its utilization. In this study, wheat straw pulp fibers were chemically crosslinked by citric acid (CA) in an environmentally friendly process. X-ray photoelectron spectroscopy and Fourier transform infrared spectra confirmed that the chemical treatment introduced carboxylic groups to cellulose fibers. Meanwhile, X-ray diffraction patterns showed that the crystallinity of cellulose was reduced. The average fiber length and water retention value of the pulp decreased with increasing CA dosage under the conditions of 3 mL/g CA 4 (4 wt% CA), and the drainage performance of the cellulose pulp improved by 21 %. Also, the crosslinking of fibers contributed to the mechanical properties of the cellulosic matrix, increasing the dry and wet strength by 21 % and 282 %, respectively. These results demonstrated that citric acid could be a sustainable method for improving the properties of wheat straw fibers, thereby promoting its application in fabricating sustainable materials., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.)

Hypochlorous acid (HClO/ClO - ) is a key reactive oxidative species (ROS) in the body. The HClO/ClO - concentrations are imbalanced during cancer formation due to the ROS stress response. This paper introduces a novel chitosan-based self-calibration fluorescent nanoprobe (ChCyNil) constructed by molecular assembly for the ratiometric detection of HClO/ClO - . Two chromophores with different fluorescence characteristics and HClO/ClO - sensitivity were labeled on chitosan, and nanoparticles were prepared by a self-assembly strategy for HClO/ClO - detection. ChCyNil exhibits several advantages, such as dual near-infrared emissions at 670 nm and 845 nm, tunable fluorescence intensity, self-calibration fluorescence, and good biocompatibility, improving its accuracy in HClO/ClO - detection. Our study confirmed that ChCyNil exhibits a well-assembled spheroidal nanostructure and good photophysical properties in solution. The fluorescence imaging properties were further proved by detecting endogenous HClO/ClO - produced by LPS/PMA stimuli in cells and zebrafish. In addition, ChCyNil was used to detect the fluorescence behavior of HClO/ClO - in tumors of live mice. The successful design and fabrication of ChCyNil have presented a new strategy for constructing detection tools with improved fluorescence properties for HClO/ClO - in live animals., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Hydrogels with remarkable flexibility have gained popularity as materials for current research. However, the unfavorable properties of short-term adhesion, susceptibility to damage, and freezing in low-temperature presented by conventional hydrogels have become bottlenecks for further applications. In this work, an anti-freezing hydrogel with excellent mechanical, adhesion, and self-healing properties were developed by constructing a persistent semiquinone/quinone-catechol redox equilibrium environment. The introduction of lignin-modified cellulose nanofibers (LCNFs) significantly improved the overall mechanical properties of the material, driven by strong hydrogen bond interactions. This enhancement was evident in the tensile properties (97.74 ± 1.72 kPa, 783 %) and compression properties (> 90 %). Within the internal network of the gel, the synergistic action of lignin and ammonium persulfate resulted in the production of catechol, which imparted the gel with excellent adhesion properties (28.26 ± 2.13 KPa) and broad adhesion applicability. In addition, the incorporation of ethylene glycol (EG) positively contributed to the strengthening of the gel while endowed with tunable anti-freezing properties. Given the exceptional advantages of the prepared hydrogels, they were used to assemble flexible strain sensors with outstanding sensitivity for monitoring human motions., Competing Interests: Declaration of competing interest The authors declare no conflict of interest., (Copyright © 2024 Elsevier B.V. All rights reserved.)

CO 2 is the main pollutant in biogas, reducing its calorific value. Among various technological methods to eliminate carbon dioxide from biogas, membrane separation technology stands out for large-scale industrial biogas purification due to its advantages. The selection of membrane material and preparation process are key factors in membrane separation technology. In this study, a premixing process was initially used to blend different masses of packed molecular sieves TS-1 (or ZSM-5) and cellulose derivatives (ethyl cellulose, cellulose acetate) separately. These mixtures were then coated onto porous PVDF substrates using a coating process to create various bilayer hybrid composite membranes. Among these, PVDF/EC-ZSM-5 (containing 15 % ZSM-5) bilayer hybrid composite membrane is the most fitting. For CO 2 /CH 4 gas mixtures, the gas selectivity of this membrane surpassed Robeson's 1991 standard line (the CO 2 permeability was 597.48 Barrer, and the CO 2 /CH 4 selectivity was 9.14). Overall, this composite membrane, made for the first time from PVDF, ZSM-5, and EC, is expected to be a promising CO 2 selective separation membrane material for biogas purification in large-scale industrial processes due to its simple production process., Competing Interests: Declaration of competing interest The authors report no declarations of interest., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Development of green packaging materials is essential to replace traditional plastics in fresh agricultural products preservation. Herein, a coated paper was designed by applying chitosan-based composite coating on paper substrate through a facile automatic coating method. The hydroxypropyl trimethyl ammonium chloride chitosan (HACC) was obtained by direct quaternization via the introduction of hydroxypropyl trimethyl ammonium chloride into the amino group of chitosan, then mixed with polyvinyl alcohol (PVA) to prepare the HACC/PVA coating. Accordingly, the key performance of coated paper were improved ascribed to the synergy effect of HACC/PVA coating and paper substrate. In particular, the minimum oxygen permeability of the coated paper could reach to 0.87 × 10 -13  cm 3 ·cm/cm 2 ·s·Pa, and the optimum water vapor permeability and tensile strength of HACC/PVA coated paper was 0.75 × 10 -12  g·cm/cm 2 ·s·Pa and 6.88 kN/m, respectively. The coated paper used as packaging material not only reduced weight loss ratio of strawberry and greengrocery, but also exhibited lower chromatic aberration and better sensory evaluation, indicating a favorable effect on fruit and vegetable storage. Taken together, the designed eco-friendly coated paper has shown tremendous potential for green and biodegradable packaging material in agricultural products preservation., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier B.V.)

Novel eco-friendly strength agent has inspired much attention of researchers. Herein, the PEI-KH560 prepared by PEI (polyethyleneimine) and KH560 (γ-glycidyl ether propyl trimethoxysilane) was added in the pulp suspension to enhance the paper performance. The results showed that the m(PEI):m(KH560) ratio and PEI's molecular weight were closely related with the paper strength and hydrophobicity. The SEM morphology of paper surface showed that the fiber-fiber crosslinking reached the tightest, at the optimal m(PEI):m(KH560) ratio and PEI's molecular weight. The results showed that when the M w (molecular weight) of PEI was 10,000 and the m(PEI):m(KH560) ratio was 1:2, the PEI-KH560 presented the best strengthening performance on the paper strength and hydrophobicity. Dry tensile index and wet tensile index could reach 29.9 N·m/g and 1.37 N·m/g after adding the PEI 10000 -KH560 in pulp suspension before the paper formation. Further, the effect of process conditions (temperature, time, the addition amount, and pulp concentration) on the strength and hydrophobicity of paper network structure was investigated, after adding PEI-KH560 into the pulp suspension. It was of great significance for studying the mechanism between the chemical structures of PEI-KH560 and paper performance, which provided valuable theoretical practice on the preparation of novel strength agent., Competing Interests: Declaration of competing interest The authors declare that they have no known competing interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Good dispersion of carbon fibers is important for the carbon paper production, which is usually achieved using low carbon fiber concentrations and disposable dispersants. In this study, we developed carbomer as a recyclable and high-efficiency dispersant for carbon fibers. When the carbon fiber concentration was 0.1 wt%, carbon fiber suspension showed improved dispersion performance as increasing the carbomer dosage. It exhibited low Turbiscan Stability Index (TSI) of 0.41 and small change of delta backscattering between -0.5 to 0.8 % when using 0.5 wt% carbomer. However, the good dispersibility fade away when increasing the concentration of carbon fibers. Subsequently, the pH of the carbon fiber suspension was adjusted to 7.0 to improve the dispersibility by increasing the viscosity, but causing a worse flowability. Then the pH was further adjusted to 13.0 to ensure good flowability in the wet-forming process and good dispersibility at carbon fiber concentration of 0.5 wt%. More importantly, the dispersant was successfully recycled and still exhibited excellent dispersion effects for carbon fibers after 5 cycles. Notably, the high-efficiency dispersion of carbon fibers and the recyclability of dispersant were achieved simultaneously for the first time, which is suitable for the eco-friendly and sustainable production of carbon paper., Competing Interests: Declaration of competing interest We declare that we have no financial and personal relationships with other people or organizations that can inappropriately influences our work. There is no professional or other personal interest of any nature or kind in any product., (Copyright © 2024 Elsevier B.V. All rights reserved.)

In recent years, flexible sensors constructed mainly from hydrogels have received increasing attention. However, conventional hydrogels need to be prepared by high-temperature or radiation-induced polymerization reactions, which limits their practical applications due to their suboptimal electrical conductivity and weak mechanical properties. In this paper, using sodium lignosulfonate as the raw material, a dynamic catechol-quinone redox system formed by lignin‑zinc ions was constructed to initiate rapid free radical polymerization of acrylamide (AM) monomer at room temperature. In addition, Deep eutectic solvent (DES) can form a strong hydrogen bonding network within the molecules and between the molecules of the hydrogel, resulting in a hydrogel with good tensile properties (hydrogel elongation at break of 727.19 %, breaking strength of 84.09 kPa), and provides the hydrogel with high electrical conductivity, anti-dehydration, anti-freezing, and anti-bacterial properties. Meanwhile, the addition of lignin also improved the adhesion and UV resistance of the hydrogel. This hydrogel assembled into a flexible sensor can sense various small and large amplitude movements such as nodding, smiling, frowning, etc., and has a wide range of applications in flexible sensors., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Castor stalk from hemp plants is an attractive lignocellulosic feedstock for biomass refining valorization due to its similar chemical composition to hardwoods. In this study, the castor stalk fibers were pretreated with efficient dual-functional ethanolamine to achieve delignification and swelling of the cellulosic fibers, followed by cellulase enzymatic digestion for biomass conversion. Experimental results showed that ethanolamine pretreatment at 160 °C for 1 h effectively removed 69.20 % of lignin and 43.18 % of hemicellulose. In addition to efficient delignification and removal of hemicellulose, the study also revealed that supramolecular structure of cellulose was another major factor affecting enzymatic hydrolysis performance. The lowered crystallinity (60-70 %) and swelled crystal sizes (2.95-3.04 nm) promoted enzymatic hydrolysis efficiency during the heterogeneous reaction process. Under optimal conditions (160 °C, 1 h; enzyme loading: 15 FPU/g substrate), promoted yields of 100 % glucose and over 90 % xylose were achieved, which were significantly higher than those obtained from untreated castor stalk. These findings highlighted the effectiveness of the dual-functional ethanolamine pretreatment strategy for efficient bioconversion of lignocellulosic feedstocks. Overall, this study provides valuable insights into the development of new strategies for the efficient utilization of biomass resources, which is essential for the sustainable development of our society., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Recently, hydrogel sensors have been widely applied in wearable and portable electronics, but the low mechanical property, intolerance of fatigue, and low sensitivity and adhesion limit their further applications. In this study, sulfonated nanocellulose (SCNF) with dual functionality was blended into polyacrylamide (PAM) hydrogel matrix to reinforce the mechanical strength and facilitate the homogeneous dispersion of carbon nanotubes (CNTs). The SCNF-CNT/PAM hydrogel was designed through free radical polymerization to achieve commendable mechanical, electrical, and multifunctional properties. The environmental-friendly SCNF serves as bio-templates to facilitate the assembling of CNT into integrated SCNF-CNT structures with good dispersity, thus enabling the establishment of an integrated conducting and reinforcing network. The fabricated SCNF-CNT/PAM hydrogel exhibited outstanding compressive strength (∼0.45 MPa at 50 % strain), tensile strength (∼169.12 kPa), and antifatigue capacity under cyclic stretching and pressing. Furthermore, the multifunctional sensors assembled using this hydrogel demonstrated high strain sensitivity (gauge factor ~ 3.7 at 100-400 % strain) and effectively detected human motions. This design principle provides promising prospects for constructing next-generation multifunctional flexible sensors, and the integration of these distinctive properties enables the prepared composite hydrogels to find potential applications in various areas, such as implantable soft electronic devices, electronic skin, and human movement monitoring., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

This study focuses on optimizing the pulping by-product to produce effective hydrogels for controlling the release of salicylic acid (SA). In this regard, two routes are achieved: the first involves preparing black liquor (BL) composite hydrogels with various polymer macromolecules [polyacrylamide (PAM), polyvinyl alcohol (PVA), and chitosan (Cs), and the second involves carboxymethylation of BL and grafting with acrylamide. Hydrogels are evaluated using spectral analysis (ATR-FTIR), thermal analysis (TGA and DTG), and swelling measures. Encapsulation, release profile, SA release kinetics, as well as ATR-FTIR and SEM measurements, were used to evaluate the behavior of loaded hydrogels. According to the results, grafted carboxymethylated BL-gel had the maximum SA release (98.7 %), followed by PAM-BL (51.7 %) and PAM/PVA-BL (43.1 %). Over a 48-hour period, the hydrogels demonstrated a prolonged SA release pattern. The Ritger-Peppas and Higuchi models fitted to all examined hydrogels showed that SA release followed both Fickian and non-Fickian diffusion pathways., Competing Interests: Declaration of competing interest Authors declare that there is no conflict among the contributing author related to the financial or non-financial interests that are directly or indirectly related to the work submitted for publication., (Copyright © 2024 Elsevier B.V. All rights reserved.)

The hybrid composite sample based on Prosopis Juliflora (PJ) bark and ramie fibre with different length, weight percentage, and curing temperature were created for the first time in this work. Totally, 120 hybrid composite samples were tested in this study. There were five different fibre lengths: 10 mm, 15 mm, 20 mm, 25 mm, and 30 mm, weight percentages 10 %, 20 %, 30 %, 40 %, and 50 %, and different curing temperatures 80 °C, 90 °C, 100 °C, 110 °C, and 120 °C used to produce the hybrid composite samples. Due to the cross-linking ability with the epoxy matrix, the hybrid composite specimen shows high resistance up to 98 Shore D hardness. The high polarity of the epoxy matrix and the hydrogen bond strengthening effect, increased the composite sample flexural strength by 12 %. The curing temperature of 100 °C, 20 mm fibre length, and 30 % of the hybrid composite sample achieved the highest tensile strength (28.76 MPa), flexural strength (46.54 MPa), impact strength (4.5 J), and hardness strength properties (98 shore D). Thermo gravimetric analysis (TGA) revealed the composite samples initial decomposition temperature (T i ) at 98 °C, maximum decomposition temperature (T max ) at 320 °C, and the final decomposition temperature (T f ) at 466 °C., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

The study examined the beneficial effects of the synergistic deinking and delignification process on the quality of recycled pulp. By utilizing a mixture of neutral sodium sulfite, sodium carbonate, and fungal hemicellulase enzyme, the research demonstrated that the paper achieved enhancements in brightness, whiteness, tensile and burst indices, while also exhibiting reduced yellowness and ERIC in comparison to paper derived from chemically deinked pulp. The high-resolution ESCA analysis demonstrated a reduction in lignin surface coverage, and enhancement in the O/C atomic ratios. FTIR spectra indicated notable alterations in the structure of fibers and the functional groups of deinked pulp fibers. XRD spectra confirmed a higher cellulose crystallinity index and FESEM micrographs illustrated a rougher surface with the emergence of new fibrils. Additionally, UV analysis of the pulp effluents indicated significant lignin absorbance, while post-bleaching with H 2 O 2 further enhanced the reactivity of the pulp and the overall quality of the paper., Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Iman Akbarpour reports financial support was provided by Gorgan University of Agricultural Sciences and Natural Resources. Iman Akbarpour reports a relationship with Gorgan University of Agricultural Sciences and Natural Resources that includes: board membership and employment. This work was funded by the Gorgan University of Agricultural Sciences and Natural Resources (GUASNR) under Project Grant AGRI/4081/2023, Research Plan ID number 01-474-93. The author extends thanks to GUASNR, Golestan University, Mazandaran University, and Tehran University for providing laboratory facilities and valuable cooperationthat contributed to the successful completion of this research. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have influenced the work reported in this paper. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

The fractionation of lignocellulose utilizing green solvents is essential for the effective operation of biorefineries. In this study, a deep eutectic solvent (DES) system composed of benzoic acid (BA, hydrogen bond donor) and choline chloride (ChCl, hydrogen bond acceptor) was fabricated and successfully applied to the lignocellulose fractionation. The DES has low toxicity and little pollution. In this system, 67.8 % of lignin and 91.2 % of hemicellulose in poplar were removed, leaving 95.8 % of cellulose intact as solid residue. Due to the removal of the amorphous components, crystallinity of cellulose-rich water-insoluble solid (CIS) substantially increased from 55.6 % to 68.6 %, and CIS was used as feedstock for nanocrystalline cellulose preparation with excellent properties. The results showed that the obtained lignin had similar properties to CEL by GPC, FT-IR, 2D-NMR and TGA. A high-purity lignin rich in G units was recovered with a well-preserved structure, which has β-O-4 linkage content up to 53.01 %, low molecular weight, low polydispersity (1.99). Finally, the hydrolyzate can be used for fermentation. This study demonstrated that BA is suitable for DES design with excellent properties on lignin extraction, and this promising DES enable efficient pretreatment for economically feasible biomass conversion. This ChCl-BA DES facilitates environmentally friendly production of functional materials derived from cellulose and lignin under mild conditions., Competing Interests: Declaration of competing interest The authors declare that they have no conflict of interest., (Copyright © 2024 Elsevier B.V. All rights reserved.)

The current study focuses on finding an ecological method to dispose of black liquors (BLs), containing lignin macromolecules, which are produced as byproducts of rice straw-based paper production. In addition to maximizing their value as precursors in the preparation of novel formaldehyde scavengers to avoid the environmental risks associated with using urea formaldehyde in agro-wood composites. To optimize the route, various black liquors are prepared from pulping of rice straw by different pulping agents (alkali, neutral, acidic and kraft reagents) used as additions or precursors for carbon compounds. Elemental analysis, thermogravimetric analysis [TGA], Fourier transform infrared [FTIR] and scanning electron microscope (SEM), are the techniques used to characterize the BLs; while the gel time, bond strength, and differential scanning calorimetry (DSC) methodologies are applied to determine the impact of black liquor (BL) and black liquor‑carbon nanostructures (BL-CNSs) on performance of urea formaldehyde (UF) adhesive. The behavior of the investigated BL-CNSs as HCHO-scavengers is assessed from their affinity to capture the HCHO, and reduction of free-HCHO in UF-palm fibers agro-composites. BL-CNSs, as novel scavengers, exhibit promising properties where the bonding strength of BL-CNSs-UF adhesives increased to 19.7 MPa even though the UF was only 8.4 MPa. Moreover, the formaldehyde adsorption capacity ranges from 35.4 to 63.6 mg/g as well as lowering the gel time. It is interesting to note that the investigated scavengers not only reduced the free-HCHO of composites by about 40-91 %, but also enhancement in their mechanical and water resistance properties; where the modulus of rupture (MOR), internal bond (IB) and reduction in thickness swelling improved to about 50 % and 83.3 %, and 38.8 %, respectively. According to the American National Standards Institute (ANSI) standard these new scavengers, especially from BL of neutral pulping, permit the production of an eco-board (E1) with static bending exceeding the H-3 class., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Lignin has attracted wide attention in sustainable environment remediation, especially the polyphenol-metal-network (PMN) based on lignin that shows unique applicability. In this work, by self-assembly of double PMN formed by lignin, plant tannins (TA) and Fe ions, a universal gravel-like lignin catalysts were reported for cost-efficient water purification. A controllable self-assembly technique dependent in pH was developed, achieving the controllable synthesis of materials with highly uniformity. Driven by strong multiple intermolecular interactions and PMN mediated TA-Fe Fenton system, this bio-based material exhibited efficient interfacial capture (65.70 mg·g -1 ) and in-situ degradation performance (95.40 %), and removed ubiquitous dye contaminants through static and flowing operation. Benefiting from this, effective flowing purify platform that continuously purify large-scale dye-containing wastewater through flowthrough strategy was profiled, confirming the potential in real industrial system. The theoretical calculations including molecular dynamics simulation contributed to providing insightful comprehension for co-assembly of system and their intermolecular interaction with dye molecules. Additionally, this material also showed magnetic response ability, stable reusability performance, and extended preparation advantages. This work provided a facile strategy to develop advanced lignin-based double PMN derived materials to support water purification by utilizing solid-waste to repair liquid-waste., Competing Interests: Declaration of competing interest We declare that we have no financial and personal relationships with other people or organizations that can inappropriately influence this work, there is no professional or other personal interest of any nature or kind in any product, service and/or company that could be construed as influencing the position presented in, or the review of, the manuscript entitled., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Compared with traditional petroleum-based foam materials, cellulosic foam materials have significant advantages in terms of economy and environmental protection. However, the traditional cellulose-based foams have some problems such as high energy consumption in the preparation process. In this study, the recycled pulp foam (RPF) with ultra-light density (12.69 kg/m 3  ~ 13.83 kg/m 3 ) and high porosity (99.07 % ~ 99.15 %) was prepared by mechanical stirring using waste corrugated cardboard as the main raw material and further hydrophobically modified using rosin. The prepared r-RPF foam has excellent hydrophobicity with the water contact angle remaining 132.9° after 20 s. In addition, the rosin coating enhances the mechanical properties of r-RPF, and the stress of r-RPF at 50 % strain is increased by 97 %. It should be noted that after rosin treatment, the compressive strength and elasticity of r-RPF were improved. The r-RPF was stable in water and had a high oil adsorption capacity (7.8 to 28.13 g/g), which had the potential to treat current oily wastewater., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Cellulose is a kind of green and renewable materials, but its flammability limits its wide application. In order to enhance the flame retardancy of cellulose materials, herein, melamine cyanurate, decabromodiphenyl ethane, 1,2-Bis(2-oxo-5,5-dimethyl-1,3,2-dioxyphosphacyclohexyl-2-imino)ethane(BODIE) and montmorillonite were used as four typical flame retardants. These flame retardants were used alone or in combination to prepare several flame retardant lyocell fibres by physical blending method. Furthermore, the flame retardancy mechanism of phosphorus, nitrogen, halogen and inorganic flame retardant was studied through TG-IR and Raman test, and the synergistic flame retardant between four flame retardants were studied for the first time. The results showed that the nitrogen and halogen-containing flame retardants played the gas-phase flame retardant action by inert gas dilution and chemical quenching of active radicals, respectively. The inorganic flame retardant exerted condensed-phase flame retardant mechanism. The phosphorus flame retardant played both gas and condensed-phase flame retardant effect by chemical quenching of active radicals and cellulose carbonization. Furthermore, the synergism index of phosphorus‑nitrogen and phosphorus-halogen in cellulose materials were 2.1 and 1.7, respectively. There was no obvious synergistic effect between inorganic flame retardant with other flame retardants. In addition, the use of any flame retardant alone tailored the fibre's Limiting Oxygen Index (LOI) lower than 28 %. In contrast, the fibres achieved a LOI of 31 % and a tensile strength of 3.0 cN/dtex when the content of phosphorous flame retardant, nitrogen flame retardant and halogen flame retardant were 45-75 %, 12-55 %, 0-25 %, respectively. This study prepared a method for preparing flame retardant cellulose materials with extremely low-cost and large-scale application potential, and provided a theoretical basis that the selection of flame retardants helped to improve the flame retardant performance of cellulose materials., Competing Interests: Declaration of competing interest The authors declared that they have no conflicts of interest to this work., (Copyright © 2024. Published by Elsevier B.V.)

In this study, polydopamine (PDA) was used to modify functional groups on the surface of carbon fiber (CF), and the effects of different dopamine hydrochloride (DPH) concentrations on the surface morphology, functional groups, contact angle and dispersion stability of CF were studied. Subsequently, the raw carbon paper (RCP), hot-pressed carbon paper (HPCP) and carbon paper (CP) were prepared successively using the modified CF through wet forming, impregnation/hot-pressing, and carbonization methods. The surface morphology, tensile strength, flexural strength, electrical resistivity, air permeability and pore size distribution were analyzed for these materials. It was observed that the introduction of -OH and - NH 2 groups improved the hydrophilicity and dispersion of PDA modified CFs, resulting in an increase in formation index (FI) from 39.2 to 48.1 for RCP samples. With increasing DPH concentration, the tensile strength of CP initially increased but then decreased while its electrical resistivity showed an opposite trend. Finally, PDA modified CP was assembled into proton exchange membrane fuel cells (PEMFC). The PEMFC assembled from DPH-CP-2.5 achieved a maximum limiting current density of 1440.0 mA/cm 2 and power density of 458.25 mW/cm 2 . Meanwhile, the lower material transmission impedance for DPH-CP-2.5 as well as excellent water management ability and gas transmission performance., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier B.V.)

Starch-based plastics offer a potential solution to environmental pollution and can reduce the dependence on petroleum-based plastics. However, effectively preparing starch-based plastics with moisture resistance and high strength remains challenging. Herein, dialdehyde starch (DAS) with different degrees of oxidation was first synthesised. The molecular weight and crystallinity of DAS decreased depending on the aldehyde content, as determined through scanning electron microscopy, X-ray diffraction and molecular weight analyses. Subsequently, a sustainable starch plastic (DAS-DA) was prepared via the dynamic imine crosslinking of DAS with diamines. The influence of the degree of oxidation of DAS on the structure and properties of DAS-DA was systematically investigated. No linear relationship was observed between the tensile strength of DAS-DA and the aldehyde content of DAS. When the aldehyde content was 41.1 %, the resulting DAS41-DA exhibited optimal mechanical strength (27.8 MPa), exceeding that of most reported starch-based plastics. In addition, owing to the presence of imine crosslinking networks, DAS41-DA exhibited excellent water and solvent resistance (>60 days), good thermal stability (456 °C-462 °C) and excellent reprocessability and biodegradability. These findings provide a theoretical basis for the preparation of high-performance bioplastics from aldehyde-containing polysaccharides., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier B.V.)

Controlling the hydrophobic behaviors of lignin nanoparticles (LNPs) is crucial and advantageous for their application as film Nano Fillers, yet it poses a significant challenge. Herein, we successfully developed a novel method for the preparation of LNPs with highly hydrophobic behaviors using ternary deep eutectic solution (DES)-H 2 O systems. The resulting LNPs exhibit a significantly reduced content of hydrophilic groups on their outer surface, leading to a zeta potential value of only -4.9 mV, and up to 140.0° of water contact angle (WCA). Afterwards, a "Dissolution-Restructuration" mechanism was proposed to explain the formation of the prepared LNPs. Firstly, DES demonstrates superior H-bonding capabilities, facilitating the complete disruption of inter- and intramolecular H-bonding in lignin, and resulting in the formation of a highly homogenized lignin network. Subsequently, the DES system undergoes compromise after adding water, triggering the reformation of both inter- and intramolecular H-bonding and π-π interactions. Consequently, lignin orderly self-assembles into LNPs with highly hydrophobic characteristics. Especially, using the as-prepared LNPs as Nano fillers, a series of LNPs-containing polyvinyl alcohol (PVA) films were successfully fabricated, exhibiting exceptional hydrophobic behaviors (with contact angles reaching up to 124.0°). Furthermore, the mechanical strength, UV-shielding capabilities, and biodegradability of the PVA films are significantly enhanced. This study introduces a sustainable and efficient approach for the synthesis of hydrophobic LNPs, thereby facilitating the broadening of applications for lignin-based functional composite film materials., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier B.V.)

Seaweed polysaccharides show tremendous research and application value because of their significant and unique biological activities. However, reports on seaweed polysaccharides usually focus on in-depth studies of a specific biological activity, which severely limits their further development. Herein, three seaweed polysaccharides were isolated from Undaria pinnatifida (UPPS), Sargassum pallidum (SPPS), and Ulva lactuca (ULPS), respectively. The physicochemical properties, structure, rheological properties, antioxidant activities, antibacterial activities, and anti-glycation activities of UPPS, ULPS, and SPPS were comprehensively studied. It was first demonstrated that SPPS and UPPS had triple prominent biological activities. SPPS exhibited the best biological activities in antioxidation (IC 50 in the ABTS test: 0.4616 ± 0.0134 mg/mL), antibacterial effect, and anti-glycation activity (inhibitory rate: 84.74 ± 0.07 %). Additionally, UPPS films (UPPSF) demonstrated superior ultraviolet shielding performance, lower water vapor permeability (1.78 ± 0.01 g/m·s·Pa × 10 -11 ), higher hydrophobicity (water contact angle: 96.91 ± 2.52°), and higher antioxidant activity compared to ULPS films (ULPSF). UPPSF and ULPSF effectively prolonged the shelf life of strawberries to six days, and UPPSF showed better preservation properties. This work provides novel theoretical insights into the use of polysaccharides as medicinal nutraceuticals, bioactive agents, and food packaging films., Competing Interests: Declaration of competing interest The authors declare no conflict of interest., (Copyright © 2024. Published by Elsevier B.V.)

Lignin is very abundant in nature, it is one of the three main components of lignocellulose, the only substance containing a benzene ring structure. Deep eutectic solvent (DES) is a considered sustainable biomass refining option, however, there is no systematic description and comparison of lignin extraction characteristics and process parameter characterization between DES process and DES combination process. This review is based on the efficient extraction of lignin by DES composed of lactic acid-choline chloride, and the process parameters and regenerated lignin properties of this DES are summarized (e.g., (a) DES composition; (b) reaction conditions; (c) raw material type; (d) third component; and (e) the combined process, and the effects on lignin extraction efficiency as well as quality). This review provides a detailed overview of the process of DES application in the field of lignin, specifically analyzing the composition, properties and synthesis methods of DES. This review also describes the structural characteristics of lignin, hemicellulose and cellulose and its solubility in DES. Finally, the outlook and direction of DES biomass refining based on the latest technology are presented., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

As biomass, rice straw (RS) is often valorized as a precursor of green products. In this respect, the RS-based carbon quantum dots (CQDs) are synthesized doped with N and S during the preparation. Synergistic doping with lipoic acid and ethylenediamine can vastly increase the yield of CQD from rice straw from 6.14 % to 62.8 %, and sulfur doping plays a more important role on the surface functional groups of the quantum dots. Further assessment is achieved toward the performance of SN-CQDs-hydroxypropyl cellulose nanocomposites. The optical behavior of synthesized SN-CQDs, and the critical concentration of its liquid crystal behaviors, at which the anisotropic phase begins to emerge, is approximately 1 %. Incorporating it into HPC, especially at 5 %, provided nanocomposite films with effective liquid crystal, tensile strength, and thermal stability. This sample's texture reveals a planar structure with colors ranging from yellow to red. The synergistic effect of incorporating SN-CQDs is shown by improving the strength to ~282.1 %, and the activation energy increased from 583.6 kJ.mol -1 to 615.1 kJ/mol. HPC-SN-CQDs can be assembled into an LED device, emitting warm light, of which CIE coordinate is (0.34,0.43)., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

In this work, shellac and its crosslinking were studied to produce paper straws for the application of liquid products. Commercial paper straws are not durable for liquid foods due to their hygroscopic nature, and thus, they find it challenging to replace single-use plastics. Shellac is a naturally occurring resin utilized as an adhesive and water-resistant coating over the paper straw. Shellac was cured at 125 °C, 150 °C, 175 °C, and 200 °C, and it was crosslinked in about 210 min, 150 min, 60 min, and 30 min respectively and studied for kinetics. The crosslinking of shellac produced a thermally stable material. Compared to commercial paper straws, these paper shellac straws exhibited high bending stiffness (1356.11 Nmm), tensile strength (13,74 MPa), flexural strength (21.72 MPa), and compression strength (24.99 MPa). Moreover, the paper shellac straws didn't bend in wet conditions under load for up to one day, while the commercial paper straw bends in 8 min. Therefore, paper straws with shellac can replace plastic-based straws for a sustainable future., Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Arihant Ahuja reports financial support was provided by the Prime Minister Research Fellowship, Ministry of Education, India. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Given the escalating environmental and safety concerns, friendly protective materials with exceptional mechanical properties, biodegradability, and insensitivity to high temperature have received more and more attention. Here, we report a robust cellulosic gel through the multi-scale integration of cellulose molecular skeleton, nano-reinforced diatomite, and in situ polymerized polyacrylamide molecule. The bottom-up yet cross-scale approach facilitates the formation of cellulosic gel characterized by a highly interconnected hydrogen bond network and nano-enhanced domain, resulting in a tensile strength of up to 13.83 MPa, a Young's modulus exceeding 280 MPa, and an impact strength around 12.38 KJ m -1 . Furthermore, this gel exhibits structural stability at temperatures up to 130 °C, good flame retardancy, and complete biodegradability within a span of 35 days. The robust cellulosic gel, acting as a pliable protector, demonstrates exceptional protection for human joints. Our study presents a highly efficient and scalable pathway towards the development of sustainable and robust biomass gels, holding immense potential in intelligent-protective wearables and advanced materials science and engineering., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

It is an interesting research topic to study the interfacial interactions between hemicellulose and cellulose, specifically how hemicellulose's structure affects its binding to cellulose nanofibers. Our research proposes that dispersion interaction play an important role in this interfacial interaction, more so than electrostatic forces when considering the adherence of cellulose to xylan. To quantify these interactions, the Atomic Force Microscope (AFM) colloidal probe technique is applied to measure the intermolecular forces between cellulose nanofibers, which are attached to the probe and xylan. These measured forces are then analyzed in relation to the length, diameter and functional groups of the nanocellulose, as well as the molecular weight and side chains of the xylan. Moreover, the predominance of dispersion forces by contrasting the adhesive forces before and after the grafting of a large nonpolar group onto xylan. This modification significantly reduces contact between the cellulose and xylan backbone, thereby markedly diminishing the dispersion interactions. Parallel to the AFM experiments, molecular dynamics (MD) simulations corroborate the experimental results and support our hypotheses. Collectively, these findings contribute to a deeper understanding of polysaccharide interactions within lignocellulose., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)