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Herein, the nanolignin-containing cellulose nanofibrils (LCNF)-enabled ratiometric fluorescent bio-nanocomposite film is developed. Interestingly, the inclusion of LCNF in the cellulose-based film enhances the detecting performance of food freshness, such as high sensitivity to biogenic amines (BAs) (limit of detection (LOD) of up to 1.83 ppm) and ultrahigh discernible fluorescence color difference (ΔE = 113.11). The underlying mechanisms are the fluorescence resonance energy transfer (FRET), π - π interaction, and cation - π interaction between LCNF and fluorescein isothiocyanate (FITC), as well as the increased hydrophobicity due to lignin, which increases the interactions of amines with FITC. Its color stability (up to 28 days) and mechanical property (49.4 Mpa) are simultaneously improved. Furthermore, a smartphone based detecting platform is developed to achieve access to food safety. This work presents a novel technology, which can have a great potential in the field of food packaging and safety., Competing Interests: Declaration of competing interest It is the original work of the authors. All the authors mutually agree that it should be submitted to Food Chemistry The manuscript has not been published or presented elsewhere in part or in entirety and is not under consideration by another journal. The authors declare that they have no conflict of interests. There is no research involving Human Participants and/or Animals., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

The high energy density and robust cycle properties of lithium-ion batteries contribute to their extensive range of applications. Polyolefin separators are often used for the purpose of storing electrolytes, hence ensuring the efficient internal ion transport. Nevertheless, the electrochemical performance of lithium-ion batteries is constrained by its limited interaction with electrolytes and poor capacity for cation transport. This work presents the preparation of a new bio-based nanofiber separator by combining oxidized lignin (OL) and halloysite nanotubes (HNTs) with polyimide (PI) using an electrospinning technique. Analysis was conducted to examine and compare the structure, morphology, thermal characteristics, and EIS of the separator with those of commercially available polypropylene separator (PP). The results indicate that the PI@OL and PI-OL@ 10 % HNTs separators exhibit higher lithium ion transference number and ionic conductivity. Moreover, the use of HNTs successfully impeded the proliferation of lithium dendrites, hence exerting a beneficial impact on both the cycle performance and multiplier performance of the battery. Consequently, after undergoing 300 iterations, the battery capacity of LiFePO 4 |PI-OL@ 10 % HNTs|Li stays at 92.1 %, surpassing that of PP (86.8 %) and PI@OL (89.6 %). These findings indicate that this new bio-based battery separator (PI-OL@HNTs) has the great potential to serve as a substitute for the commonly used PP separator in lithium metal batteries., 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.)

Widely employed petroleum-based food packaging materials have inflicted irreparable harm on ecosystems, primarily stemming from their non-biodegradable attributes and recycling complexities. Inspired by natural nacre with a layered aragonite platelet/nanofiber/protein multi-structure, we prepared high-barrier composite films by self-assembly of cellulose nanofibrils (CNF), cellulose nanocrystals (CNC), montmorillonite (MMT), polyvinyl alcohol (PVA) and alkyl ketene dimer (AKD). The composite films demonstrated outstanding barrier properties with oxygen vapor transmission of 0.193 g·mm·m -2 ·day -1 and water vapor transmission rates of 0.062 cm 3 ·mm·m -2 ·day -1 ·0.1 MPa -1 , which were significantly lower than those of most biomass-degradable packaging materials. Additionally, the impacts of mixing nanocellulose with various aspect ratios on the tensile strength and folding cycles of the films were examined. The exceptional resistance of the composite films to oil and water provides a novel and sustainable approach to reduce non-biodegradable plastic packaging., 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 Ltd. All rights reserved.)

Cellulose acetate (CA)-based electrospun nanofiber aerogel (ENA) has drawn extensive attention for wastewater remediation due to its unique separation, inherent porosity and biodegradability. However, the low mechanical strength, poor durability, and limited adsorption ability hinder its further applications. We herein propose using silane-modified ENA, namely T-CA@Si@ZIF-67 (T-ENA), with enhanced resilience, hydrophobicity, durability and hetero-catalysis to remediate a complex wastewater containing oil and drug residues. The robust T-ENA was fabricated by pre-doping tetraethyl orthosilicate (TEOS) and ligand in its spinning precursors, followed by in-situ anchoring of porous ZIF-67 on the electrospun nanofibers (ENFs) via seeding method before freeze-drying and thermal curing (T). Results show that the T-ENA displays enhanced mechanical stability/resilience and hydrophobicity without compromise of its high porosity (>98 %) and low density (10 mg/cm 3 ) due to the silane cross-linking. As a result, the hydrophobic T-ENA shows over 99 % separation efficiency towards different oil-water solutions. Meanwhile, thanks to the enhanced adsorption-catalytic ability and the activation of peroxymonosulfate (PMS) from the porous ZIF-67, fast degradation of carbamazepine (CBZ) residue in the wastewater can be achieved within 20 min. This work might provide a novel strategy for developing CA aerogels to remove organic pollutants., 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 Ltd. All rights reserved.)

The electrospinning technology has set off a tide and given rise to the attention of a widespread range of research territories, benefiting from the enhancement of nanofibers which made a spurt of progress. Nanofibers, continuously produced via electrospinning technology, have greater specific surface area and higher porosity and play a non-substitutable key role in many fields. Combined with the degradability and compatibility of the natural structure characteristics of polysaccharides, electrospun polysaccharide nanofiber membranes gradually infiltrate into the life field to help filter air contamination particles and water pollutants, treat wounds, keep food fresh, monitor electronic equipment, etc., thus improving the life quality. Compared with the evaluation of polysaccharide-based nanofiber membranes in a specific field, this paper comprehensively summarized the existing electrospinning technology and focused on the latest research progress about the application of polysaccharide-based nanofiber in different fields, represented by starch, chitosan, and cellulose. Finally, the benefits and defects of electrospun are discussed in brief, and the prospects for broadening the application of polysaccharide nanofiber membranes are presented for the glorious expectation dedicated to the progress of the eras., 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.)

Compared with traditional papermaking, foam forming is a new papermaking technology that uses foam instead of water to disperse fibres, which can effectively solve the problem of poor evenness of ceramic paper, but the instability of foam itself affects the application of foam forming technology. Herein, a highly stable foaming agent for foam forming technology was prepared via physical reaction of lauryl dimethyl amine oxide (OB-2) with filamentous nanocellulose (cellulose nanofiber (CNF-C) and bacterial cellulose (BC)). Then, the quartz paper was prepared by foam forming technology. Firstly, hydrogen bond interactions between hydroxyl groups of the filamentous nanocellulose and hydrophilic moieties on OB-2 enabled the formation of a 3D nanonetwork layer on the surface of the bubble, which extended the half-life of the bubble and effectively prevented the bubble from bursting or coalescing. Then, the foam was extruded and cracked, and the filamentous nanocellulose was retained on the quartz fibres to prepare filamentous nanocellulose/quartz fibre paper by foam forming technology. The quartz paper exhibited excellent evenness and mechanical properties. In conclusion, the research of foam forming technology is of great significance to the application and development of special 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.)

Airborne particulate matter is a pressing environmental and public health concern globally. This study aimed to develop sustainable filtration materials from cellulose nanofibers (CNFs) modified with graphene oxide (GO) to capture fine particulates from air effectively. CNFs were extracted from α-cellulose via mechanical grinding and modified with 0.5-1.5 wt% GO solution by ultrasonication to produce CNF-GO nanocomposites. These were freeze-dried into highly porous, lightweight aerogels for air filtration applications. Fourier transform infrared spectroscopy (FT-IR) confirmed GO incorporation through hydroxyl group interactions. Field emission scanning electron microscopy (FE-SEM) revealed a porous 3D network with reduced porosity after GO addition due to pore blocking. X-ray diffraction analysis showed the cellulose I crystal structure was retained after modification. Brunauer-Emmett-Teller (BET) measurements indicated increased density but decreased surface area and pore volume with GO loading. The thermogravimetric analysis demonstrated improved thermal stability with GO incorporation due to oxidative reactions and a barrier effect. The particulate absorption efficiency markedly increased from 86.37 % to 99.98 % for CNFs modified with 1.5 wt% GO due to the high surface area, surface oxygen functionalities, and nanoplatelet morphology of GO. The nanofiber filters with 1.5 wt% GO exhibited a maximum absorption efficiency of 99.98 % and a quality factor of 0.0912 Pa -1 . Although GO reduced biodegradability, substantial degradation occurred under soil conditions. Overall, the sustainable, high-efficiency CNF-GO air filters developed in this work demonstrate immense promise for controlling air pollution and protecting human health., 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, carboxylated and amination modified cellulose nanofibrils (CNFs) were fabricated via the TEMPO catalytic oxidation system and diethylenetriamine, and collagen composite aerogels were fabricated through a simple self-assembly pretreatment and directional freeze-drying technology. Morphology analysis showed that the collagen composite aerogels had distinct layered-oriented double network structures after the self-assembly pretreatment. The intermolecular interactions between the collagen fibrils and functionalized CNFs (fCNFs) on the structures and properties of the composite aerogels were also examined through various characterization techniques. Water contact angle tests demonstrated the pH-responsive characteristics of the collagen/fCNF composite aerogels. Using 5-fluorouracil as the model drug, the pH-response mechanism was revealed. These results indicated that the collagen/fCNF composite aerogels exhibited excellent pH-responsive drug release capacities. Therefore, these pH-responsive collagen composite aerogels might have potential applications in industrial production in the biomedical, drug delivery, and tissue engineering fields., Competing Interests: Declaration of competing interest The authors report no declarations of interest., (Copyright © 2024 Elsevier B.V. All rights reserved.)

The development of advanced nanofluidic membranes with better ion selectivity, efficient energy conversion and high output power density remains challenging. Herein, we prepared nanofluidic hybrid membranes based on TEMPO oxidized cellulose nanofibers (T-CNF) and manganese-based metal organic framework (MOF) using a simple in situ synthesis method. Incorporated T-CNF endows the MOF/T-CNF hybrid membrane with a high cation selectivity up to 0.93. Nanoporous MOF in three-dimensional interconnected nanochannels provides massive ion transport pathways. High transmembrane ion flux and low ion permeation energy barrier are correlated with a superior energy conversion efficiency (36 %) in MOF/T-CNF hybrid membrane. When operating under 50-fold salinity gradient by mixing simulated seawater and river water, the MOF/T-CNF hybrid membrane achieves a maximum power density value of 1.87 W m -2 . About 5-fold increase in output power density was achieved compared to pure T-CNF membrane. The integration of natural nanofibers with high charge density and nanoporous MOF materials is demonstrated an effective and novel strategy for the enhancement of output power density of nanofluidic membranes, showing the great potential of MOF/T-CNF hybrid membranes as efficient nanofluidic osmotic energy generators., 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 © 2023 Elsevier B.V. All rights reserved.)

Electro-conductive hydrogels emerge as a stretchable conductive materials with diverse applications in the synthesis of flexible strain sensors. However, the high-water content and low cross-links density cause them to be mechanically destroyed and freeze at subzero temperatures, limiting their practical applications. Herein, we report a one-pot strategy by co-incorporating cellulose nanofiber (CNF), Poly pyrrole (PPy) and glycerol with polyvinyl alcohol (PVA) to prepare hydrogel. The addition of PPy endowed the hydrogel with good conductivity (∼0.034 S/m) compared to the no PPy@CNF group (∼0.0095 S/m), the conductivity was increased by 257.9 %. The hydrogel exhibits comparable ionic conductivity at -18 °C as it does at room temperature. It's attributed to the glycerol as a cryoprotectant and the formation of hydrated [Zn(H 2 O) n ] 2+ ions via strong interaction between Zn 2+ and water molecules. Moreover, the cellulose nanofiber intrinsically assembled into unique hierarchical structures allow for strong hydrogen bonds between adjacent cellulose and PPy polymer chains, greatly improve the mechanical strength (stress∼0.65 MPa, strain∼301 %) and excellent viscoelasticity (G'max ∼ 82.7 KPa). This novel PPy@CNF-PVA hydrogel exhibits extremely high Gauge factor (GF) of 2.84 and shows excellent sensitivity, repeatability and stability. Therefore, the hydrogel can serve as reliable and stable strain sensor which shows excellent responsiveness in human activities monitoration., 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 © 2023. Published by Elsevier B.V.)

Air pollution is a major environmental and public health issue. Each year, large amounts of particulate matter (PM) and other harmful pollutants are released into the atmosphere. Conventional polymer nanofiber filters lack the functionality to capture ultrafine PM. As a sustainable alternative, this work developed titanium dioxide (TiO 2 ) nanoparticle surface-modified cellulose nanofiber (CNF) aerogels for PM 2.5 filtration. CNFs were extracted via mechanical disintegration to diameters below 100 nm. The nanofibers were functionalized with 1.0-2.5 wt% TiO 2 nanoparticles using citric acid cross-linking. Cylindrical aerogels were fabricated by freezing and lyophilizing aqueous suspensions. Structural, morphological, thermal, and mechanical properties were characterized. TiO 2 modification increased density (11.8-19.7 mg/cm 3 ), specific surface area (287-370 m 2 /g), and Young's modulus (33.5-125.5 kPa) but decreased porosity (99.6 %-97.7 %), pore size (20.2-15.6 nm) and thermal stability compared to unmodified cellulose aerogels. At 2.5 wt% loading, the optimized aerogels achieved 100 % absorption of 0.1-5 μm particulates owing to reduced pore size. Despite enhanced filtration capabilities, the modified CNF aerogels retained inherent biodegradability, degrading over 70 % within one month of soil burial. This pioneering research establishes TiO 2 functionalized CNF aerogels as promising sustainable alternatives to traditional petroleum-based air filters, representing an innovative approach to creating next-generation nanofiltration materials capable of effectively capturing fine and ultrafine particulate matter pollutants., 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 © 2023 Elsevier B.V. All rights reserved.)

Electrospinning nanofibers membrane has received much attention to remove the insoluble oil from the sewage, while the poor mechanical strength and low oil/water separation efficiency of membranes limit their practical application. Here, we prepared a superwettable deacetylated cellulose acetate (d-CA)-based electrospinning nanofibers membrane simply dipped by bacterial cellulose (BC) and cross-linked with citric acid (CCA) to construct the spider-web structure spontaneously. Compared with the pristine d-CA membrane, the obtained d-CA/BC@CCA membrane exhibits the remarkable oil/water separation performance. The flux and separation efficiency of n-hexane/water emulsion without (SFE) and with (SSE) emulsifier for d-CA/BC@CCA membrane are 9364 L·m -2 ·h -1 ·bar -1 , 98.34 % and 5479 L·m -2 ·h -1 ·bar -1 , 99.39 %, respectively, which are mainly attributed to the improved hydrophilicity of its surface and the decreased pore sizes caused by the unique spider-web structure. In addition, d-CA/BC@CCA membrane also possesses the outstanding mechanical properties, the better cycle stability, as well as the excellent durability. This study provides a novel strategy for the construction of the high-performance oil/water separation membrane., 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 © 2023 Elsevier B.V. All rights reserved.)

Reverse electrodialysis (RED) using nanofluidic ion-selective membrane may convert the salinity difference between seawater and river water into electricity. However, heterogeneous modification reactions of cellulose commonly leads to the inhomogeneous distribution of surface charges, thereby hampering the improvement of cellulose-based nanofluidic membranes for energy conversion. Herein, RED devices based on cellulose nanofibers (CNF) membranes with opposite charge characteristics were developed for the generation of salinity gradient power. Anion-CNF membrane (A-CNF) with varying negative charge densities was synthesized using 2,2,6,6-Tetramethylpiperidine 1-oxy radical (TEMPO) oxidation modification, whereas cation-CNF membrane (C-CNF) was prepared through etherification. By mixing artificial seawater and river water, the output power density of CNF RED device is up to 2.87 W m -2 . The output voltage of 30 RED units connected in series may reach up to 3.11 V, which can be used to directly power tiny electronic devices viz. LED lamp, calculator, etc. The results of this work provide a feasible possibility for widespread application of ion exchange membranes for salinity gradient energy harvesting., 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 © 2023 Elsevier B.V. All rights reserved.)

Nanocellulose of different morphologies was extracted from Sunn Hemp (Crotalaria Juncea) using acid hydrolysis. The work focused on two objectives: first, to valorize the Sunn Hemp fibers for nanocellulose (NC) production, and second, to study the effects of acid concentration on different morphologies of NC and their properties. The study extracted nanocellulose at five different concentrations of H 2 SO 4 : 16 %, 32 %, 48 %, 64 %, and 72 %. Obtained nanocellulose was characterized by Scanning Electron Microscopy (FE-SEM), Atomic Force Microscopy (AFM), Fourier Transform Infrared Spectroscopy (FTIR), X-ray Diffraction (XRD) and Thermogravimetric Analysis (TGA). AFM and FE-SEM confirmed the production of three different morphologies of nanocellulose. The NC-32 had a web-like structure typically observed for cellulose nanofibrils (CNF), whereas NC-48 and NC-64 were observed as cellulose nanocrystals (CNC) with rod-like and needle-like shapes, respectively, and NC-72 displayed spherical particles termed cellulose nanospheres (CNS). The total crystallinity index of NC was calculated using FTIR, and a similar trend of crystallinity was also observed from XRD analysis. NC-32 was obtained with the highest yield of 94.83 %, followed by 91.40 % and 81.70 % for NC-48 and NC-64, respectively, whereas NC-72 yielded the lowest yield of 12.03 %. NC-72 had the highest thermal stability among other NC morphologies., Competing Interests: Declaration of competing interest The authors declare that there are no conflicts of interest., (Copyright © 2023 Elsevier B.V. All rights reserved.)

Direct addition of disinfectants and membrane separation techniques have been common methods to address microbial contamination in water. However, disinfectants may generate toxic by-products, and even minor damage or biofilm formation on filtration membranes can lead to a heightened risk of microbial contamination. Consequently, how to quickly and safely disinfect microbial contaminated water sources remains a huge challenge. In this study, the high-strength broad-spectrum antibacterial CNF/CS composite membrane was fabricated by utilizing cellulose nanofibers (CNF) to reinforce the structure of chitosan (CS). The resulting CNF/CS composite membrane exhibits an impressive tensile strength of 148 MPa and boasts an active chlorine content of 5.29 %. Notably, even after undergoing 50 washing cycles and 10 repeated chlorination procedures, the structural integrity and high active chlorine content of the composite membrane remain preserved, validating its exceptional strength, stability, and chlorine rechargeability. Additionally, the CNF/CS antibacterial materials demonstrate remarkable attributes in terms of rapid sterilization, sustained and consistent release of active chlorine, and efficient inhibition of biofilm formation, demonstrating great potential in efficient, green, and safe sterilization., 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 © 2023. Published by Elsevier B.V.)

The use of polyelectrolytes is emerging as a fascinating strategy for the functionalization of biomedical membranes, due to their ability to enhance biological responses using the interaction effect of charged groups on multiple interface properties. Herein, two different polyelectrolytes were used to improve the antibacterial properties of polycaprolactone (PCL) nanofibers fabricated via electrospinning. First, a new cationic cellulose derivative, cellulose-bearing imidazolium tosylate (CIMD), was prepared via the nucleophilic substitution of the tosyl group using 1-methylimidazole, as confirmed by NMR analyses, and loaded into the PCL nanofibers. Secondly, sodium alginate (SA) was used to uniformly coat the fibers' surface via self-assembly, as remarked through SEM-EDX analyses. Polyelectrolyte interactions between the CIMD and the SA, initially detected using a FTIR analysis, were confirmed via Z potential measurements: the formation of a CMID/SA complex promoted a substantial charge neutralization of the fibers' surfaces with effects on the physical properties of the membrane in terms of water adsorption and in vitro degradation. Moreover, the presence of SA contributed to the in vitro response of human mesenchymal stem cells (hMSCs), as confirmed by a significant increase in the cells' viability after 7 days in the case of the PCL/CMID/SA complex with respect to the PCL and PCL/CMID membranes. Contrariwise, SA did not nullify the antibacterial effect of CMID, as confirmed by the comparable resistance exhibited by S. mutans , S. aureus, and E. coli to the PCL/CIMD and PCL/CIMD/SA membranes. All the reported results corroborate the idea that the CIMD/SA functionalization of PCL nanofibers has a great potential for the fabrication of efficient antimicrobial membranes for wound healing.

Multistimuli-responsive fluorescent materials have garnered great research interest benefited from their practical applications. Two twisted-structure compounds containing tetraphenylethylene (TPE) as the aggregation-induced emission (AIE) group and a pyridine unit as the acid reaction site to obtain new multistimuli-responsive fluorescent compounds (namely, TPECNPy: TPECNPy-2 and TPECNPy-3) were successfully synthesized through a one-step Knoevenagel condensation reaction. The multiple-stimuli response process of TPECNPy was investigated by means of photoluminescence (PL) spectra and emission colour. The results showed that both TPECNPy compounds with excellent AIE abilities displayed reversible emission wavelength and colour changes in response to multiple external stimuli, including grinding-fuming by CH 2 Cl 2 or annealing and HCl-NH 3 vapour fuming. More importantly, fluorescent nanofibre films were prepared by electrospinning a solution of TPECNPy mixed with cellulose acetate (CA), and these exhibited reversible acid-induced discolouration, even with only 1 wt% TPECNPy. The results of this study may inspire strategies for designing multistimuli-responsive materials and preparing fluorescent sensing nanofibre films., (© 2023 John Wiley & Sons Ltd.)

The landfilling of paper mill sludge (PMS) has been restricted or even banned in many countries due to the raised concern about greenhouse gas (GHG) emissions and contamination of the soil and water, calling for a sustainable PMS management approach. The potential valorization of PMS to nanomaterials combined with traditional biorefinery was examined in this work. Three types of PMS-derived cellulose nanofibrils (CNFs) were prepared and evaluated: enzymatically assisted CNF (AU: with in-house produced enzyme and CT: with commercial enzyme), mechanically pretreated CNF (BT), and chemically pretreated CNF by TEMPO oxidation (TEMPO). It was found that enzyme-assisted mechanical fibrillation-derived CNFs had a comparable average diameter (27.9 nm for AU and 22.7 nm for CT) with that produced from mechanical pretreatment (26.5 nm for BT) and TEMPO oxidation pretreatment (20.0 nm for TEMPO), and they showed the best drainage properties among the three types of CNF. The CNFs resulting from enzymatic pretreatment reduced 15% of energy consumption compared to the mechanical method and had better thermostability than TEMPO oxidation method. In addition, the on-site produced enzyme showed similar performance to the commercial enzymes towards the CNF properties. These findings provide new insights into a promising integrated strategy in engineering CNF from PMS with on-site enzyme production as a novel and sustainable approach for PMS management and valorization., 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 © 2023 Elsevier Ltd. All rights reserved.)

Today, one of the world's critical environmental issues is air pollution, which is the most important parameter threatening human health and the environment. Synthetic polymers are widely used in industrial air filter production; however, they are incompatible with the environment due to their secondary pollution. Using renewable materials to manufacture air filters is not only environmentally friendly but also essential. Recently, a new generation of biopolymers called cellulose nanofiber (CNF)-based hydrogels have been proposed, with three dimensional (3D) nanofiber networks and unique physical and mechanical properties. CNFs have become a hot research topic for application as air filter materials because they can compete with synthetic nanofibers due to their advantages, such as abundant, renewable, nontoxic, high specific surface area, high reactivity, flexibility, low cost, low density, and network structure formation. The main focus of the current review is the recent progress in the preparation and employment of nanocellulose materials, especially CNF-based hydrogels, to absorb PM and CO 2 . This study summarizes the preparation methods, modification strategies, fabrications, and further applications of CNF-based aerogels as air filters. Lastly, challenges in the fabrication of CNFs, and trends for future developments 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 © 2023 Elsevier B.V. All rights reserved.)

Tobacco based cellulose nanofiber (TCNF) is a novel nanocellulose that has recently been used to replace undesirable wood pulp fibers in the preparation of reconstructed tobacco sheets (RTS). However, given the strict requirements for controlling toxic chemical content in tobacco products, there is a global interest in developing a green, efficient, and toxic-chemical free approach to isolate TCNF from tobacco stem as a bioresource. In this study, we propose a creative and environmentally friendly method to efficiently and safely isolate TCNF from tobacco stem pulp, which involves integrated biological pretreatment followed by a facile mechanical defibrillation process. Feruloyl esterase is used to pretreat the stem pulp by disrupting the ether and ester bonds between lignin and polysaccharide carbohydrates within the fiber wall, which effectively facilitates cellulase hydrolysis and swelling of the stem pulp fiber, as well as the following mechanical shearing treatment for TCNF isolation. The results demonstrate that TCNF obtained by the comprehensive feruloyl esterase/cellulase/mechanical process exhibit uniform and well-dispersed nanofiber morphology, higher crystallinity, and stronger mechanical properties than those of the control. The addition of 0.5 % TCNF can replace wood pulp by 18 wt% ~ 25 wt% in the production of RTS samples while maintaining their reasonable strength properties., Competing Interests: Declaration of competing interest The authors declare that they have no know competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Pollution from particulate matter (PM) and toxic chemicals in the air cause some of the most critical health and environmental hazards in developed and developing countries. It can have a very destructive effect on human health and other living creatures. In particular, PM air pollution caused by rapid industrialization and population growth is a grave concern in developing countries. Oil and chemical-based synthetic polymers are non-environmentally friendly materials that lead to secondary environmental pollution. Thus, developing new and environmentally compatible renewable materials to construct air filters is essential. The goal of this review is to study the use of cellulose nanofibers (CNF) to adsorb PM in the air. Some of CNF's advantages include being the most abundant polymer in nature, biodegradable, and having a high specific surface area, low density, surface properties (broad possibility of chemical surface modification), high modulus and flexural stiffness, low energy consumption, which provide this new class of bio-based adsorbent with promising potential applications in environmental remediation. Such advantages have made CNF a competitive and highly in-demand material compared to other synthetic nanoparticles. Today, refining membranes and nanofiltration manufacturing are two important industries that could use CNF to provide a practical step in protecting the environment and saving energy. CNF nanofilters are capable of nearly eliminating most sources of air pollution, including carbon monoxide, sulfur oxides, nitrogen oxides, and PM 2.5 - 10 μm. They also have a high porosity and low resistance air (pressure drop) ratio compared to ordinary filters made from cellulose fiber. If utilized correctly, humans do not need to inhale harmful chemicals., 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 © 2023. Published by Elsevier B.V.)

The applications of hydrogels are prominently affected by the modulation of their structure and performance. We herein systematically implemented the modulation of an all-polysaccharide hydrogel consisting of TEMPO-oxidized cellulose nanofibers (TOCN) and cationic guar gum (CGG). Four different factors including the carboxylate content and size of TOCN, the freezing-thawing treatment and solid content of hydrogel were studied to disclose their influence on the structure and property of TOCN/CGG hydrogel. The results indicated that the increase of carboxylate content of TOCN, the number of freezing-thawing cycles and solid content all increased the crosslinking density of hydrogel as a result of the improved interactions. Accordingly, the hydrogels exhibited more compact structures and enhanced rheological properties. The influence of TOCN size on the hydrogel structure and property was demonstrated to be dependent on the compromise between the exposed functional groups of TOCN and their ability in generating entanglements inside the hydrogel. This work helps shed light on the modulation of hydrogel structure and performance, which might facilitate the exploration of hydrogel applications., Competing Interests: Declaration of competing interest There is no conflict of interest to declare., (Copyright © 2023 Elsevier B.V. All rights reserved.)

Bee propolis is one of the most common natural extracts and has gained significant interest in biomedicine due to its high content of phenolic acids and flavonoids, which are responsible for the antioxidant activity of natural products. The present study report that the propolis extract (PE) was produced by ethanol in the surrounding environment. The obtained PE was added at different concentrations to cellulose nanofiber (CNF)/poly(vinyl alcohol) (PVA), and subjected to freezing thawing and freeze drying methods to develop porous bioactive matrices. Scanning electron microscope (SEM) observations displayed that the prepared samples had an interconnected porous structure with pore sizes in the range of 10-100 μm. The high performance liquid chromatography (HPLC) results of PE showed around 18 polyphenol compounds, with the highest amounts of hesperetin (183.7 µg/mL), chlorogenic acid (96.9 µg/mL) and caffeic acid (90.2 µg/mL). The antibacterial activity results indicated that both PE and PE-functionalized hydrogels exhibited a potential antimicrobial effects against Escherichia coli, Salmonella typhimurium, Streptococcus mutans, and Candida albicans. The in vitro test cell culture experiments indicated that the cells on the PE-functionalized hydrogels had the greatest viability, adhesion, and spreading of cells. Altogether, these data highlight the interesting effect of propolis bio-functionalization to enhance the biological features of CNF/PVA hydrogel as a functional matrix for biomedical applications., (© 2023. The Author(s).)

Traditional hydrophobic binders can limit supercapacitors' performance by impeding ion accessibility. Herein, we demonstrate the potential of plant-derived environmentally friendly Cellulose Nanofibers (CNF) as binders for biochar (BN-Ac)-based supercapacitors. The CNF binder retains BN-Ac's micropores and improves wettability, while the Polyvinylidene Fluoride (PVDF) binder fills micropores and hinders ion-conductive pathways. The as-synthesized BN-Ac/CNF exhibits a capacitance of 268.4 F g -1 at 5 A g -1 , which is 1.4 times higher than that of BN-Ac/PVDF. In addition, the energy density improves from 4.6 to 5.7 Wh kg -1 at 2.1 and 2.5 kW kg -1 power, respectively, for replacing PVDF with CNF. More importantly, BN-Ac/CNF shows outstanding capacitance retention of 96.2 % after 10,000 charge/discharge cycles. The improved wettability and reduced bulk electrolyte resistance by hydrophilic CNF binders are responsible for the electrode's high capacitance. Concurrently, this study showcases a facile strategy for improving supercapacitor performance and a green application of CNF in energy devices., Competing Interests: Declaration of competing interest The authors declare that they have no conflicts of interest to this work., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Biomedical materials are in high demand for transplantation in cases of diseased or damaged bone tissue. Hydrogels are potential candidates for bone defect repair; however, traditional hydrogels lack the necessary strength and multiple functions. Herein, we effectively synthesized a cellulose nanofiber (CNF)-reinforced oxidized alginate (OSA)/gelatin (Gel) semi-interpenetrating network hydrogel through a facile one-step approach without a cross-linker by using the synergistic effects of dynamic imine bonds and hydrogen bonds. The OSA/Gel/CNF sample showed a notable compressive modulus (up to 361.3 KPa). The gelation time (~150 s) ensured excellent injectability. Self-healing exhibited a high efficiency of up to 92 %, which would enable minimally invasive, dynamic adjustments and personalized therapies. Furthermore, the OSA/Gel/CNF hydrogel showed excellent biomineralization (Ca/P ratio ~ 1.69) and enhanced preosteoblast cell (MC3T3-E1) viability (over 96 %), proliferation, and osteogenic differentiation. Thus, this multifunctional hydrogel has promising potential for using in the bone tissue repairs., 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 © 2022 Elsevier Ltd. All rights reserved.)

Novel phase change materials composed of polyethylene glycol (PEG), cellulose nanofibers (CNFs) and carbon nanotubes (CNTs) were developed by an efficient and environment friendly strategy. The CNFs were modified and cross-linked by chitosan to form three-dimensional network structure, which provides strong support for the resulting CNF/CNT/PEG composites. The structure and properties of CNF/CNT/PEG composites were characterized using scanning electron microscopy, spectrums, and differential scanning calorimeter. They exhibit high latent heat (158.3 J/g), low heat loss (0.75%) and excellent photo-thermal conversion (energy storage efficiency 85.6%), electro-thermal conversion (energy storage efficiency 92.3%) properties. Due to their excellent performances, CNF/CNT/PEG composites have great potential to be used as thermal management 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 © 2022 Elsevier Inc. All rights reserved.)

Inspired by nacre-layered nanostructure, 1D 2,2,6,6-tetramethyl-1-piperidinyloxy (TEMPO)-oxidized cellulose nanofibers (TOCNFs) were used as the template to assemble 2D MXene nanosheets into a layered TOCNF/MXene nanocomposite film by a vacuum-assisted filtration strategy. The synergistic effect of the MXene "brick" and TOCNFs "mortar" endowed the composite film with excellent flexibility and a tensile strength of 128.13 MPa, which were attributed to interactions between the interconnected three-dimensional network and multiple hydrogen bonds between TOCNFs and MXene. The humidity-sensing mechanism of the sensor involved the swelling/contraction of channels between MXene interlayers induced by adsorbed H 2 O and the swelling of TOCNFs. The TOCNF/MXene sensor showed a maximum response (-ΔI/I 0 ) of 90 % under 97 % RH, outstanding bending and folding durability (up to 50 cycles), and long-term stability. Lastly, the sensor could dynamically monitor human respiration, skin, and fingertip humidity, suggesting its promising applications in smart wearable electronics., 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 © 2022 Elsevier Ltd. All rights reserved.)

The degree of polymerization (DP) of cellulose plays an essential role in unlocking the superior mechanical potential of wood cellulose nanofibrils (CNFs). However, severe degradation of cellulose chains during the chemical pulping is a big challenge to obtain CNFs with high DP. In this work, we tend to improve the DP of wood CNFs by significantly preserving the native structure of wood fibers in an industrial method. Wood sticks are first pretreated with hydrothermal treatment to partially remove hemicellulose, thus leading to an increased porous structure that facilitates the penetration of cooking liquid and lignin removal during delignification, and dilute-alkali-sulfate pulping is then employed to obtain wood fibers with highest viscosity average DP (DP V ) of nearly 2400. After that, the as-prepared wood fibers with high DP are separated into CNFs with highest average DP V of 1333. Finally, we demonstrate the potential application of wood CNFs with improved DP V in the fabrication of strong and tough isotropic films and macrofibers., 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 © 2022 Elsevier Ltd. All rights reserved.)

Osmotic energy reserves in estuaries, coupled with the ubiquitous solar energy, could be harnessed through emerging nanofluidic membranes to reduce the energy crisis. Herein, we mixed WS 2 with high concentration of metal phase and cellulose nanofiber (CNF) to fabricate composite membranes by vacuum filtration. Incorporated CNF as space charge donors increases the ion flux through the enlarged interlayer spacing in the WS 2 /CNF composite membrane. By simulating seawater and river water, the power density of the composite membrane reached to 1.99 W m -2 . Furthermore, due to the photoelectric characteristics of WS 2 , the composite membrane exhibits photoresponsivity, which generated a photocurrent of 177 nA through illumination. Taking the advantage of the optoelectronic properties of the composite membrane, the power density under illumination is twice than that of the dark state. Based on the results, this material design strategy can enhance the ion transport in nanofluidic membranes for efficient generation of clean energy., 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 © 2022 Elsevier Ltd. All rights reserved.)

Post-fibrillation endoglucanase treatment was employed to reduce the entanglement of cellulose nanofibrils (CNFs) produced with low extent of mechanical milling. The results showed that post-fibrillation endoglucanase treatment can effectively reduce the fibril degree of polymerization (DP) values and therefore entanglement. Cellulose DP was reduced from 520 for CNFs prepared by milling using a SuperMassColloider with 1 pass to 225 after endoglucanase treatment at a low dosage of 1 mg protein/g fibril for 24 h. Endoglucanase treatment can also effectively reduce the fibril mean diameter from 66 nm to 25 nm. Applying post-fibrillation endoglucanase treatment produced more uniform CNFs than the feed CNFs from pure mechanical treatment. All CNFs suspensions prepared by post-fibrillation endoglucanase treatment were non-Newtonian (except at very low concentrations below 0.5 wt%) with shear thinning behavior. Post-fibrillation endoglucanase treatment reduced the viscosity of CNF suspensions due to decreasing fibril DP values and the extent of entanglement., (Copyright © 2022. Published by Elsevier Ltd.)

Sargasso cellulose nanofibers (CNFs) and polyvinyl alcohol (PVA) components were composed to generate novel KCNF/PVA films by a simple and benign crosslinking strategy. Sargasso CNFs are a potential reinforcement material due to its extremely long length (15-20 μm) and natural nanostructure. The low water resistance of PVA limits their use in humid and watery environments. However, the chemical cross-linking between sargasso CNFs and PVA consumes a large number of hydrophilic hydroxyl groups, the resulting KCNF/PVA films exhibited outstanding water resistance (water contact angle 119°). Especially, the wet strength of KCNF/PVA films (50 MPa) was raised by 92 times when compared to that of pristine PVA films (0.54 MPa). Furthermore, these KCNF/PVA films could be dissolved and recycled easily. The regenerated films also show outstanding mechanical performance., (Copyright © 2022. Published by Elsevier Ltd.)

The effect of cellulose nanofibers (CNFs)/polyvinyl alcohol (PVA) coating on the hydrophobic, oleophobic, and strength properties of paper were investigated. The results showed that the size of bamboo fibers (BFs) decreased significantly and the crystallinity increased significantly after biological enzyme treatment. The average length of CNFs obtained by high pressure homogenization was 2.4 µm, the diameter was 28.7 nm, and the crystallinity was 63.63%. When the coating weight of PVA/CNF was 2.0 g/m 2 and the CNF dosage was increased from 0.0% to 3.0%, the paper grease resistance grade was increased from 7 to 9, the Cobb value was decreased from 22.68 ± 0.29 g/m 2 to 18.37 ± 0.63 g/m 2 , the contact angle was increased from 67.82° to 93.56°, and the longitudinal and transverse tensile index were increased from 67.72 ± 0.21 N m/g and 37.63 ± 0.25 N m/g to 68.61 ± 0.55 N m/g and 40.71 ± 0.78 N m/g, respectively. When the CNF dosage was 3.0% and the coating weight of PVA/CNF was 4.0 g/m 2 , the grease resistance grade of the paper was 12, the Cobb value was 21.80 ± 0.39 g/m 2 , and the longitudinal and transverse tensile indices were 72.11 ± 0.43 N m/g and 42.58 ± 0.48 N m/g, respectively. In summary, the increase of CNFs can effectively improve the lipophobicity, hydrophobicity and tensile strength of the PVA coated paper., (© 2022. The Author(s).)

In this study, we developed a humidity sensor with high sensitivity based on cellulose nanofiber/carbon nanotube (CNF/CNT) hybrid foam. The porous structure of the foam not only provides more contact interface for water molecules adsorption, but also tunes the conductivity of the CCF closed to the point where the sensor is most sensitive to the change in humidity. With this porous structural design, the obtained foam sensor shows a high humidity sensitivity of 87.3% (ΔI/I 0 , and the response limit is 100%), excellent linearity (R 2  = 0.996) within the humidity range from 29 to 95% relative humidity (RH), and good long-time stability (more than two months). Furthermore, the water vapor adsorption behavior of the CNF/CNT foam sensor can be well described by the pseudo-first-order kinetic model. Finally, a simple humidity measuring device based on the CNF/CNT foam is presented, which can find good applications for human breath and fingertip humidity monitoring., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

The scale-up preparation of aramid nanofiber (ANF) and cellulose nanofiber (CNF), still faces serious challenges such as extreme production cost and lengthy preparation cycle. Herein, a feasible top-down strategy was proposed to achieve the efficient reclamation of waste resources, further realizing the large-scale production of high value-added nanofibers. The ANF/CNF as nanoscale building blocks and their reinforcement effects on the mechanical performances of carbon fiber/phenolic composites were investigated. Related strength and modulus of ANF/CNF-enhanced composites in the tensile, bending, shear and nano indentation tests, increased by 118.1% (tensile strength), 141.2% (tensile modulus), 142.2% (flexural strength), 354.4% (flexural modulus), 38.8% (shear strength) and 94.4% (elastic modulus), respectively. Our work offers a valuable reference in the fabrication of low-cost ANF/CNF derived from waste resources, which would facilitate the wide application of nanofibers in fabricating high-performance advanced functional materials., (Copyright © 2022. Published by Elsevier Ltd.)

In this paper, based on the TEMPO oxidated Cellulose Nanofiber (TOCNF)/ɛ-poly-l-lysine (ɛ-PL) cross-linking network and citric acid as the cross-linking agent, aerogel material was designed. Citric acid (CA) can be used as a multifunctional cross-linking agent with TOCNF esterification cross-linking, and with TOCNF and ɛ-PL hydrogen bond cross-linking, but also as a reinforcing agent to improve mechanical and antibacterial properties. When the ɛ-PL content reached 0.8%, the tensile strength of the aerogel increased from 12.03 MPa to 26.44 MPa, while the elongation at break decreased to 29.33%. As the amount of ɛ-PL increased, the thermal decomposition temperature of aerogel rose to 215 °C. Aerogels had a high antibacterial efficiency (above 99.9%). After 28 days, aerogels can be biodegraded in the soil. More importantly, the aerogel had a hemolysis rate of less than 5%, indicating that the prepared degradable cellulose aerogel was a material with good blood compatibility. It had huge application potential in medical environment and food packaging., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Lignin-containing cellulose nanofibrils (LCNFs) with tunable lignin contents from sugarcane bagasse were directly prepared by low-temperature soda‑oxygen pulping combined with simple mechanical treatment. The residual lignin structure, morphology and physical dimensions of LCNFs, and properties of the relevant cellulose nanopapers (CNPs) were investigated. In situ 2D Heteronuclear Single Quantum Coherence (HSQC) NMR spectra showed β-O-4 linkages, ferulate, and para-coumarate were well preserved in the LCNFs. Compared with the cellulose nanofibrils (CNFs), LCNFs displayed a more uniform size and narrow diameter distribution. The corresponding CNPs exhibited outstanding mechanical properties (tensile strength reached 152.9 MPa), and excellent combined optical properties both in the UV blocking and visible light transparency. Moreover, the water contact angles (50.0-80.2°) of LCNFs were much higher than that of CNFs (21.7°). Direct preparation of LCNFs under mild condition would unlock the full potential of cellulosic materials and provide enhanced opportunities for cellulose to fabricate multi-functional and high-value materials., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

The fabrication of commercial cellulose nanofibrils (CNFs) into arrays with long-range ordering is of great significance for their extended applications, which, however, is severely hindered by their high disorder, aggregation, and hornified features. Herein, sub-nanoscale anionic metal oxide clusters (phosphotungstic acid, H 3 PW 12 O 40 , PTA) are applied to complex with commercial CNFs (dried powder DCNF and aqueous suspension WCNF) in aqueous media, and a long-range ordered layer structure can be facilely fabricated via typical unidirectional freezing. The surface complexation of the commercial CNFs and PTA can be confirmed through the small-angle scattering studies of the complex hydrogels. The hydrogels present similar correlation lengths in small-angle X-ray and neutron scattering measurements, suggesting the homogeneous distribution of PTA along the commercial CNFs. This gives rise to the negatively charged surface feature and further leads to strong repulsion among the commercial CNFs. Due to the disparity in sizes, the influence of PTA on the density of hydrogel networks is suppressed, and the network density is mainly dependent on the mass content of CNFs. The studies provide guidance to fabricate hydrogels with catalytic and photosensitive properties and also to design and stabilize long-range ordered structured aerogels during the removal of the nonfreezing bound water absorbed by the commercial CNFs after unidirectional freezing. This facile strategy shows great potential to broaden the application of commercial CNFs in thermal insulators, super-adsorbent materials, and supercapacitors in electrical devices.

Mineral fillers hinder cellulosic fiber bonding and thus limit the increase of filler content in paper. Herein, precipitated calcium carbonate (PCC)/cellulose nanofibrils (CNF) composites were fabricated by a facile and efficient strategy, i.e., co-refining process (CRP). During this process, CNF and PCC were activated by mechanochemical effect and formed encapsulation structure by calcium ion coordination and hydrogen bonding. The encapsulation structure and H-bond/ionic coordination interactions not only endowed the composite with excellent size stability but also enhanced interfacial interaction between composite fillers and cellulosic fibers. Compare with the paper filled with only PCC, PCC + CNF mixture, the tensile index of the cellulosic paper containing PCC/CNF composite was increased by 44.48% and 12.14%, respectively. These results not only provide a facile and scalable approach to increase interaction between cellulosic fiber and mineral filler but also create more possibilities for special paper-based materials with requiring high content of inorganic materials., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Collagen (Col) films were reinforced by celluloses in different geometries: microcrystalline cellulose (MCC), cellulosic fines (CF), cellulose nanofiber (CNF) and cellulose nanocrystals (CNC). The reinforcement mechanisms were investigated by the elastoplasticity and fracture appearance. Compared with the fracture stress of collagen film (67.5 MPa), the Col-CNF films effectively borne the stress (95.8 MPa) by intercrystalline fracture, ascribing the abundant hydrogen bonding and mechanical locking between cellulose and collagen. The toughness of Col-CF films was increased by the interfibrillar slippage of CF and pull-off of CF within the matrix, improving the strain-to-break from 8.37% to 12.13%. The films added with MCC and CNC weaken the mechanical behavior, due to the defects and lack of mechanical locking. Besides, the effects of celluloses' geometries on the thickness, density, water-tightness, thermal stability, crystallinity and FTIR of films were also investigated. These provide the evidence that the geometries of fillers diversely improve the behaviors of collagen film offering strategies for the film with adjustable mechanical properties., (Copyright © 2022. Published by Elsevier B.V.)

We hypothesized that use of a composite three-dimensionally (3D) printed scaffold with electrospun nanofibers in conjunction with recipient-site preconditioning with an external volume expansion (EVE) device would enable successful dermal tissue regeneration of a synthetic polymer scaffold. Cell viability, cell infiltration, extracellular matrix deposition, scaffold contraction, and mRNA expression by dermal fibroblasts cultured on three different scaffolds, namely, 3D-printed scaffold with a collagen coating, 3D-printed scaffold with an electrospun polycaprolactone nanofiber and collagen coating, and 3D-printed scaffold with an electrospun polycaprolactone/collagen nanofiber, were measured. Before scaffold implantation, rats were treated for 2 h with an EVE device to evaluate the effect of this device on the recipient site. Cell proliferation rates were significantly higher on the 3D-printed scaffold with electrospun polycaprolactone nanofiber and collagen coating than on the other scaffolds. In cell invasion studies, the 3D-printed scaffold with electrospun polycaprolactone nanofiber and collagen coating showed better cell integration than the other scaffolds. Under stereomicroscopy, fibroblasts adhered tightly to the electrospun area, and the fibroblasts effectively produced both collagen and elastin. Rat skin treated with an EVE device exhibited increased HIF-1α protein expression and capillary neoformation compared with control skin. Invasion of CD8 + cytotoxic lymphocytes surrounding the scaffold decreased when the recipient site was preconditioned with the EVE device. The composite 3D printed scaffold with electrospun nanofibers provided a favorable environment for proliferation, migration, and extracellular matrix synthesis by fibroblasts. Recipient-site preconditioning with an EVE device allowed for scaffold incorporation with less inflammation due to improved angiogenesis.

The capture of radioactive iodine has recently attracted much attention due to the release of radioactive iodine during nuclear waste disposal and disasters. Exploring highly efficient, sustainable, and eco-friendly materials for capturing radioactive iodine has great significance in developing safe nuclear energy. We reported highly efficient, natural, lignin-based, electrospun nanofibers (LNFs) for reversible radioiodine capture. Abundant iodine adsorption sites, such as functional groups and the interaction between the intermolecular forces exist in LNFs. The capacity of the LNFs for the saturated adsorption of iodine was found to be 220 mg·g -1 , which is higher than that of the majority of bio-based adsorbents studied. Moreover, the LNFs exhibited an excellent recycling behavior, and their absorption capacity remained at 84.72% after 10 recycles. Therefore, the results imply that the lignin-based nanofibers can act as a natural, sustainable and eco-friendly packed material for the purification columns in industrial applications. The results demonstrate that the novel, nanostructured, natural biomass, as an ideal candidate has the potential for practical nuclear wastewater purification., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Carbon nanofibers (CNFs) have been paid much attention as supercapacitor electrode due to outstanding chemical stability, high electron transfer rate and large specific surface area. However, the preparation process of CNFs is always stalemated in electrospinning, heat stabilization and carbonization. The problems of solvent pollution in the electrospinning process, complex process and high energy consumption in conventional carbonization process can't be solved. Herein, CNFs have been innovatively prepared from nanofibrillated cellulose by the molten-salt method (NaCl/NaOH). Molten salt penetrates between the fibers, separates and activates the fibers. The obtained carbon nanofibers remain developed branching structures and have a large specific surface area (899 m 2  g -1 ). The electrical properties are tested in a symmetrical two-electrode system. The specific capacitance is 150 F g -1 at the current density of 1 A g -1 . Low equivalent series resistance (1.13 Ω) indicates that it has high electrode conductivity. This study has taken into account energy conservation, environmental protection, recyclability and simplified preparation process, which has a very far-reaching significance for the industrial production of CNFs., (Copyright © 2022. Published by Elsevier B.V.)

The poor dispersibility and re-dispersibility of cellulose nanofibrils (CNFs) in various solvents and polymers have been recognized as the key factors limiting their potential applications. TEMPO oxidation, as the most common surface modification, can greatly improve the dispersion and re-dispersion of CNFs. However, the diameter of TEMPO-oxidized cellulose nanofibers (TOCNFs) has not been regulated in most researches, which was an important factor determining the dispersion and re-dispersion of TOCNFs. Herein, this work explored the effect of carboxyl groups on dispersion and re-dispersion of TOCNFs with uniform diameter in various solvents. Notably, fractal dimension was innovatively introduced to characterize the distribution of TOCNFs diameter. The fractal dimension and statistic diameter of TCONFs with different carboxyl group contents are ~1.56 and ~22 nm, demonstrating that the diameter of TOCNFs has been regulated in the same range. When the carboxyl group content is up to 1.58 mmol/g, the dispersion and re-dispersion of TOCNFs suspension in water and different organic solvents are the most uniform and stable. In a word, this work explores the dispersion and re-dispersion of TOCNFs with the uniform diameter and different carboxyl group contents, which can provide the theoretical guidance for various potential applications of nanofibrils in polymer matrix composites., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Polyoxometalate (POM) presents great potential in oxidative desulfurization (ODS) reaction. However, the high dissolubility of POM in common solvents makes it difficult to recycle. Besides, the small specific surface area of POM also limits the interaction between them and the substrate. Depositing polyoxometalates onto three-dimensional (3D) network structured materials could largely expand the application of POM. Here, the surfaces of cellulose nanofibrils (CNFs) were modified with very few (3-Aminopropyl) trimethoxysilane (APTS) to endow positive charges on the surfaces of CNFs, and then phosphotungstic acid (PTA) was loaded to obtain the aerogel A-CNF/PTA as the ODS catalyst. FT-IR indicated the successful deposition of PTA onto aminosilane modified CNF surfaces. UV-VIS further suggested the stability of PTA in the aerogels. BET and SEM results suggested the increased specific surface area and the relatively uniform 3D network structure of the prepared aerogels. TGA analysis indicated that the thermal stability of the aerogel A-CNF/PTA50% was a little higher than that of the pure CNF aerogel. Most importantly, the aerogel A-CNF/PTA50% showed good catalytic performance for ODS. Catalysis results showed that the substrate conversion rate of the aerogel A-CNF/PTA50% reached 100% within 120 min at room temperature. Even after five cycles, the substrate conversion rate of the aerogel A-CNF/PTA50% still reached 91.2% during the dynamic catalytic process. This work provides a scalable and facile way to stably deposit POM onto 3D structured materials.

Nanofilters made with high adsorption freeze-dried modified cellulose nanofiber (CNF) aerogel were produced. The modification was made using functional groups containing phthalimide, and then their ability to adsorb particulate matter (PM) was evaluated and compared with the control filter (HEPA). The results showed that the highest adsorption of PM 2.5 (99.95%) belonged to the nanofilters made of 1.5% phthalimide-modified CNF aerogel, and the lowest adsorption (76.66%) was related to the control samples. Moreover, based on the results, the nanofilter produced from freeze-dried phthalimide-modified CNF aerogel showed high filtration efficiency as well as excellent resistance to temperature and humidity. This modification enables the filter to operate in different environmental conditions, especially for particles less than 0.1 μm that are mainly responsible for reducing air quality, human health, air visibility, and climate change. In conclusion, we developed an environmentally friendly biodegradable nanofilter capable of high-performance filtration functions and structural stability in different environmental conditions., (Copyright © 2022 Elsevier B.V. All rights reserved.)

The conservation of historical paper objects with high cultural value is an important societal task. Papers that have been severely damaged by fire, heat, and extinguishing water, are a particularly challenging case, because of the complexity and severity of damage patterns. In-depth analysis of fire-damaged papers, by means of examples from the catastrophic fire in a 17th-century German library, shows the changes, which proceeded from the margin to the center, to go beyond surface charring and formation of hydrophobic carbon-rich layers. The charred paper exhibits structural changes in the nano- and micro-range, with increased porosity and water sorption. In less charred areas, cellulose is affected by both chain cleavage and cross-linking. Based on these results and conclusions with regard to adhesion of auxiliaries, a stabilization method is developed, which coats the damaged paper with a thin layer of cellulose nanofibers. It enables the reliable preservation of the paper and-most importantly-retrieval of the contained historical information: the nanofibers form a flexible, transparent film on the surface and adhere strongly to the damaged matrix, greatly reducing its fragility, giving it stability, and enabling digitization and further handling., (© 2022 The Authors. Small published by Wiley-VCH GmbH.)

Increased attention has evoked on the utilization of renewable energy, particularly osmotic power as a potential solution to the energy crisis and environmental pollution. Herein, we fabricate graphitic carbon nitride (g-C 3 N 4 )/cellulose nanofiber (CNF) composite membranes with tailored lamellar nanochannels for capturing osmotic energy from salinity gradients. Composite membranes exhibiting charge-governed ion conductivity were prepared via co-homogenization of g-C 3 N 4 with CNF and vacuum filtration. Ion conductivity was efficiently modulated by fine-tuning the charge density through controlling the weight content of CNF in the composite membranes. Higher ion conductivity of 0.014 S cm -1 at low concentrations (<10 -2  M KCl) was achieved due to the increased charge density of the lamellar nanochannels and the excellent aqueous stability of the membranes. We demonstrate the potential of the composite membranes in nanofluidic osmotic energy conversion, displaying thermo-enhanced power output performance. This work could inspire new designs of cellulose-based nanofluidic devices for improved osmotic energy conversion., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Excessive bleeding in traumatic hemorrhage is the primary concern for natural wound healing and the main reason for trauma deaths. The three-dimensional (3D) bioprinting of bioinks offers the desired structural complexity vital for hemostasis activity and targeted cell proliferation in rapid and controlled wound healing. However, it is challenging to develop suitable bioinks to fabricate specific 3D scaffolds desirable in wound healing. In this work, a 3D composite scaffold is designed using bioprinting technology and synergistic hemostasis mechanisms of cellulose nanofibrils (TCNFs), chitosan, and casein to control blood loss in traumatic hemorrhage. Bioinks that consist of casein bioconjugated TCNF (with a casein content of 104.5 ± 34.1 mg/g) using the carbodiimide cross-linker chemistry were subjected to bioprinting for customizable 3D scaffold fabrication. Further, the 3D composite scaffolds were in situ cross-linked using a green ionic complexation approach. The covalent conjugation among TCNF, casein, and chitosan was confirmed by Fourier transform infrared (FTIR) spectroscopy, nuclear magnetic resonance (NMR), X-ray photoelectron spectroscopy (XPS), sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), and X-ray diffraction (XRD) studies. The in vitro hemostasis activity of the 3D composite scaffold was analyzed by a human thrombin-antithrombin (TAT) assay and adsorption of red blood cells (RBCs) and platelets. The 3D composite scaffold had a better swelling behavior and a faster whole blood clotting rate at each time point than the 3D TCNF scaffold and commercial cellulose-based dressings. The TAT assay demonstrated that the 3D composite scaffold could form a higher content of thrombin (663.29 pg/mL) and stable blood clot compared to a cellulosic pad (580.35 pg/mL), 3D TCNF (457.78 pg/mL), and cellulosic gauze (328.92 pg/mL), which are essential for faster blood coagulation. In addition, the 3D composite scaffold had a lower blood clotting index (23.34%) than the 3D TCNF scaffold (41.93%), suggesting higher efficiencies for RBC entrapping to induce blood clotting. The in vivo cytocompatibility was evaluated by a 3D cell culture study, and results showed that the 3D composite scaffold could promote growth and proliferation of NIH 3T3 fibroblast cells, which is vital for wound healing. Cellulase-based in vitro deconstruction of the 3D composite scaffold showed significant weight loss (80 ± 5%) compared to the lysozyme hydrolysis (22 ± 5%) after 28 days of incubation, suggesting the biodegradation potential of the composite scaffold. In conclusion, this study proposes efficient prospects to develop a 3D composite scaffold from bioprinting of TCNF-based bioinks that can accelerate blood clotting and wound healing, suggesting its potential application in reducing blood loss during traumatic hemorrhage.

Ionic conductive hydrogels have been widely applied in sensors, energy storage and soft electronics recently. However, most of the polyvinyl alcohol (PVA) based ionic hydrogels are mainly fabricated by soaking the hydrogels in high concentration electrolyte solution which can induce the waste of electrolyte and solvent. Herein, we have designed cellulose nanofibrils (CNF) and ZnSO 4 reinforced PVA based hydrogels through a one-pot simple freezing-thawing method at low ZnSO 4 concentration without any soaking process. Furthermore, the hydrogel with 0.4% CNF exhibited stress up to 0.79 MPa (242% strain) and high ionic conductivity of 0.32 S m -1 (0.07 M ZnSO 4 ). Moreover, hydrogel sensor displayed high linear gauge factor 1.70 (0-200% strain), excellent stability, durability and reliability. The integrated hydrogel sensor also showed excellent sensor performance for human motion monitoring. This work provides a new prospect for the design of cellulose reinforced conductive hydrogels via a facile method., (Copyright © 2021. Published by Elsevier Ltd.)

Recently, the high-value utilization of food wastes has attracted great interest in sustainable development. Focusing on the major application of electrochemical energy storage (ECES), light-weight lignin-based carbon nanofibers (LCNFs) were controllably fabricated as supercapacitors from melon seed shells (MSS) and peanut shells (PS) through electrospinning and carbonizing processes. As a result, the optimal specific capacitance of 533.7 F/g in three-electrode system, energy density of 69.7 Wh/kg and power density of 780 W/Kg in two-electrode system were achieved. Surprisingly, the LCNFs also presented a satisfied electromagnetic absorption property: The minimum reflection loss (RL) value reached -37.2 dB at an absorbing frequency of 7.98 GHz with an effective frequency (RL < 10 dB) of 2.24 GHz (6.88 to 9.12 GHz) at a thickness of 3.0 mm. These features make the multifunctional LCNFs highly attractive for light-weight supercapacitor electrodes and electromagnetic wave absorbers applications., (Copyright © 2021 Elsevier B.V. All rights reserved.)