Cellulose Nanofibers Research Articles

Enhancing strength and toughness simultaneously: Diblock-grafted cellulose nanofiber one-component nanocomposites

To overcome the drawbacks of homopolymer-grafted CNF one-component nanocomposites, a range of diblock-grafted cellulose nanofiber (CNF), CNF-g-(polybutyl acrylate-b-polymethyl methacrylate)s were synthesized through reversible-deactivation radical polymerization (RDRP) methods. The chemical structures and ratios between the two blocks were confirmed, with surface-grafted CNF observed as submicron particles. Both thermal and thermodynamic analysis revealed two glass transition temperatures (Tg) in the diblock-grafted CNF, and phase-separated morphology was observed in the nanocomposites. The densely grafted CNF displayed island structures, while sparsely grafted samples transitioned into continuous structure. Thermodynamic analysis showed that the diblock-grafted CNF nanocomposites maintained mechanical properties at high temperatures. These nanocomposites demonstrated robust strength and toughnes, with tensile strength reaching as high as 43.7 ± 1.6 MPa and elongation at break of 70.3 ± 16.2 %. Moreover, while densely grafted CNF exhibited higher modulus and strength, whereas sparsely grafted CNF displayed behavior more reminiscent of thermoplastic elastomers, indicated by lower modulus and higher elongation.

Pickering emulsions stabilized by cellulose nanofibers with tunable surface properties for thermal energy storage

Cellulose nanofibers (CNFs) have been widely used as a renewable emulsifier to stabilize two immiscible liquids due to their intrinsic amphiphilicity and excellent emulsifying ability. However, it remains challenging to fully understand the effects of carboxylate group content and surface charge density on the emulsifying ability of CNFs and the stability of Pickering emulsion. Herein, carboxymethylated CNFs were extracted from bleached kraft pulp using etherification reaction and high-pressure homogenization, allowing for easy surface charge density and size adjustment by changing sodium chloroacetate content and homogenization cycles. The optimizing CNFs possessed a high Zeta potential (−71.2 mV) and a suitable carboxylate group content (1.81 mmol/g), which enabled CNFs to irreversibly adsorb at the hydrophobic paraffin wax (PW) droplet surface and form interfacial steric barriers, providing large electrostatic repulsion between the PW droplets against coalescence. Thus, the CNF-stabilized PW emulsions could be stored for more than 6 months. Moreover, the phase change enthalpy of the freeze-dried emulsion is as high as 193.7 J/g, which provides the emulsion to reversibly store and release heat. This work provides a comprehensive insight into the interfacial stability mechanism of CNFs as stabilizers and facilitates the potential application in thermal energy storage.

Cellulose Acetate-Based Wound Dressings Loaded with Bioactive Agents: Potential Scaffolds for Wound Dressing and Skin Regeneration.

Wound healing and skin regeneration are major challenges in chronic wounds. Among the types of wound dressing products currently available in the market, each wound dressing material is designed for a specific wound type. Some of these products suffer from various shortcomings, such as poor antibacterial efficacy and mechanical performance, inability to provide a moist environment, poor permeability to oxygen and capability to induce cell migration and proliferation during the wound healing process. Hydrogels and nanofibers are widely reported wound dressings that have demonstrated promising capability to overcome these shortcomings. Cellulose acetate is a semisynthetic polymer that has attracted great attention in the fabrication of hydrogels and nanofibers. Loading bioactive agents such as antibiotics, essential oils, metallic nanoparticles, plant extracts, and honey into cellulose acetate-based nanofibers and hydrogels enhanced their biological effects, including antibacterial, antioxidant, and wound healing. This review reports cellulose acetate-based hydrogels and nanofibers loaded with bioactive agents for wound dressing and skin regeneration.

Application of bacterial-derived long cellulose nanofiber to suspension culture of mammalian cells as a shear protectant

Nanofibrillated bacterial cellulose (NFBC) is a bio-compatible long-fiber nanocellulose produced by cellulose-synthesizing bacteria. It forms an entangled network structure in the suspension state, thereby imparting greater viscosity than conventional media additives. In this study, we examined its application as a shear protectant in the suspension culture of mammalian cells to mitigate hydrodynamic stress imposed on the cells. The media supplemented with hydroxypropyl cellulose-adsorbed NFBC (HP-NFBC) exhibited an increase in shear viscosity according to rheometric analysis, similar to FP003, a commercially available medium additive. Suspension culture of Chinese hamster ovary cells in HP-NFBC-containing media under a high stirring rate (120 rpm) demonstrated higher cell growth and lower cell death compared to those in the medium without additives and in FP003. A 0.10 (w/v)% concentration of HP-NFBC showed the highest viable cell number among the tested concentrations. Computational fluid dynamics simulation revealed a decrease in shear rate and flow velocity within the spinner flask owing to the addition of HP-NFBC or FP003. It is suggested that the decline of these parameters in high-viscosity media suppresses the hydrodynamic stress on cells. This study highlights the potential of HP-NFBC as a shear protectant in mammalian cell suspension culture.

A bio-based, self-healable, conductive rubber film with oxidized cellulose nanofiber segregated network

Rubber composites are indispensable in all areas of our daily lives. However, the formation of permanent crosslinked networks in rubber materials makes it difficult to recycle, resulting in a non-negligible waste of resources. In this paper, a vulcanization-free, fully bio-sourced rubber composite was prepared by using oxidized natural rubber (oNR) and oxidized cellulose nanofibers (TOCFs). TOCFs are selectively dispersed between the latex particles to form a segregated network. Meanwhile, the formation of hydrogen-bonding between oxygenated polar groups of oNR and abundant hydroxyl and carboxyl groups of TOCFs improves their interfacial interactions. This special structure promotes strain-induced crystallization (SIC) behavior of oNR matrix, giving its tensile strength up to 14.7 MPa. Furthermore, the oNR/TOCFs film shows excellent self-healing efficiency (96 %) at 40 °C for 5 h. The hygroscopicity of the TOCFs segregated network can turn the oNR/TOCFs film to be a conductive film by regulating the absorbed water content. The film has high conductivity (0.05 S/m) at a water content of 8.99 wt%, and the resistance change (RV/R0) can be varied between 1–5.9 × 10−6 at a water content range of 0–8.99 wt%, which makes it have potential for a wide range of humidity monitoring applications.

Enhanced Electromagnetic Energy Conversion in an Entropy‐driven Dual‐magnetic System for Superior Electromagnetic Wave Absorption

AbstractThermochemical conversion is a highly effective method for upgrading organic solid wastes into high‐value materials, contributing to carbon neutrality and peak, carbon emission goals. It also serves as a pathway to develop energy‐efficient electromagnetic wave absorbing (EMWA) materials. In this study, fish skin to successfully in situ nitrify Prussian Blue into Fe3N under external thermal driving condition, resulting in high saturation magnetization is utilized. The resulting Fe3N@C demonstrates outstanding EMWA property, achieving a minimum reflection loss of −71.3 dB. Furthermore, by introducing cellulose nanofiber, a portion of the iron nitride is transformed into iron carbide, resulting in Fe3C/Fe3N@C. This composite exhibits enhanced EMWA properties owing to wider local charge redistribution and stronger electronic interactions, achieving an effective absorption bandwidth (EAB) of 6.64 GHz. Electromagnetic simulations and first‐principles calculations further elucidate the EMWA mechanism, and the maximum reduction value of the radar‐cross section reached 37.34 dB·m2. The design of multilayer gradient metamaterials demonstrated an ultra‐broadband EAB of 11.78 GHz. This paper presents an efficient strategy for atomic‐level biomass waste utilization to prepare Fe3N, provides novel insights into the conversion between metal nitrides and metal carbides, and offers a promising direction for the development of advanced EMWA materials.

Olive pomace upcycling: Eco-friendly production of cellulose nanofibers by enzymatic hydrolysis and application in starch films.

Olive pomace (OP) waste, produced in large quantities, contains significant amounts of cellulose and fibers, making it a valuable resource for developing reinforcing ingredients in biodegradable packaging materials. This study aimed to produce nanofibers from OP using enzymatic hydrolysis with hemicellulases and cellulases, and to incorporate these nanofibers into starch films as a reinforcing agent. Cellulose nanofibers (CNFs) were prepared by alkaline pretreatment followed by enzymatic hydrolysis (with hemicellulases and cellulases) from olive pomace and applied as reinforcement in starch films in concentrations of 0.5%-5% (w/v). The nanofibers were analyzed according to composition, structural, and thermal properties. The nanofibers' suspension presented a cloudy and white color in aqueous suspension, the X-ray diffraction (XRD) analysis showed the increase of crystallinity, and the fibers' range was no wider than 100nm (according to Scherer equation). The composition analysis showed the decrease of carbonyl groups of hemicellulose and lignin. The starch films presented a homogenous surface. The solubility from these biodegradable films significantly reduced after the incorporation of CNF, and the nanomaterial's presence improved the degradation temperature (from 310°C to 322°C) and the mechanical resistance because the tension of rupture increased from 3.79 to 6.21MPa. PRACTICAL APPLICATION: The utilization of waste from the olive pomace for cellulose nanofiber production holds promise, given the nanofibers' ability to readily integrate into various materials, including starches used in biodegradable film production. Within these matrices, nanofibers act as structure reinforcers and significantly reduce the solubility of films. Although biodegradable films ensure the shelf life, safety, and quality of food, their properties currently do not match those of traditional petroleum-based materials at an industrial scale, indicating a need for further enhancement.

Bacterial cellulose-graphene oxide composite membranes with enhanced fouling resistance for bio-effluents management

Bacterial cellulose composites hold promise as renewable bioinspired materials for industrial and environmental applications. However, their use as free-standing water filtration membranes is hindered by low compressive strength, fouling, and poor contaminant selectivity. This study investigates the potential of bacterial cellulose-graphene oxide composites membranes for fouling resistance in pressure-driven filtration. Graphene oxide dispersed in poly(ethylene glycol) (PEG-400) is incorporated as a reinforcing filler into 3D network of bacterial cellulose using an in-situ synthesis method. The effect of graphene oxide on in situ fermentation yield and the formation of percolated-network in the composites shows that the optimal membrane properties are reached at a graphene oxide loading of 2 mg/mL. The two-dimensional graphene oxide nanosheets uniformly dispersed into the matrix of bacterial cellulose nanofibers via hydrogen-bonded interactions demonstrated nearly twofold higher water flux (380 L m−2 h−1) with a molecular weight cut-off ranging between 100–200 KDa and a sixfold increase in wet compression strength than pristine BC. When exposed to synthetic organic foulants and bacterial rich feed solutions, the composite membranes showed more than 95% flux recovery. Additionally, the membranes achieved over 95% rejection of synthetic natural organic matter and bacterial rich solutions, showcasing their enhanced fouling resistance and selectivity.

Isolation and Characterization of Novel Cellulose Micro/Nanofibers from Lygeum spartum Through a Chemo-Mechanical Process

Recent studies have focused on the development of bio-based products from sustainable resources using green extraction approaches, especially nanocellulose, an emerging nanoparticle with impressive properties and multiple applications. Despite the various sources of cellulose nanofibers, the search for alternative resources that replace wood, such as Lygeum spartum, a fast-growing Mediterranean plant, is crucial. It has not been previously investigated as a potential source of nanocellulose. This study investigates the extraction of novel cellulose micro/nanofibers from Lygeum spartum using a two-step method, including both alkali and mechanical treatment as post-treatment with ultrasound, as well as homogenization using water and dilute alkali solution as a solvent. To determine the structural properties of CNFs, a series of characterization techniques was applied. A significant correlation was observed between the Fourier transform infrared (FTIR) spectroscopy and X-ray diffraction (XRD) results. The FTIR results revealed the elimination of amorphous regions and an increase in the energy of the H-bonding modes, while the XRD results showed that the crystal structure of micro/nanofibers was preserved during the process. In addition, they indicated an increase in the crystallinity index obtained with both methods (deconvolution and Segal). Thermal analysis based on thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) confirmed improvement in the thermal properties of the isolated micro/nanofibers. The temperatures of maximum degradation were 335 °C and 347 °C. Morphological analysis using a scanning electron microscope (SEM) and atomic force microscope (AFM) showed the formation of fibers along the axis, with rough and porous surfaces. The findings indicate the potential of Lygeum spartum as a source for producing high-quality micro/nanofibers. A future direction of study is to use the cellulose micro/nanofibers as additives in recycled paper and to evaluate the mechanical properties of the paper sheets, as well as investigate their use in smart paper.

Optimization of a Solvent Exchange Method Enabling the Use of Dehydrated Cellulose Nanofibers as the Thickener in Lubricating Oleogels

A method that enabled the formulation of lubricating oleogels using dried cellulose nanofibers (CNFs) as an eco-friendly thickener in castor oil was studied. In their dehydrated state, strong hydrogen bonding between nanofibers and high hydrophilicity are the main obstacles to their dispersion in oil. Hence, clusters of dried CNFs had to be previously detached by their dispersion in water. The resulting hydrogels were then subjected to methanol washes to displace the water from the nanofibers. After centrifugation, the methanol-wetted precipitate was readily dispersed in castor oil, forming an oleogel once the methanol was removed. Optimization was conducted in terms of the following variables: (a) hydrogel processing method; (b) hydrogel pH; (c) methanol/hydrogel ratio; (d) number of washes; and (e) oleogel CNF concentration. Their effect on the oleogel linear viscoelastic behavior was analyzed. In general, they demonstrated a prevailing elastic behavior denoted by a well-developed plateau region. The CNF concentration was found to have a more remarkable impact on the oleogels’ rheological behavior than any other variable studied. Hence, substantial differences were observed between 1 and 2 wt.%. The CNFs exhibited a very remarkable thickening capacity in castor oil, achieving a plateau modulus of ca. 700 Pa with just 2 wt.%. Moreover, the resulting oleogels maintained a uniform texture even after one year of storage. This indicates that the oleogels were both homogeneous and storage stable, effectively overcoming the stability issues associated with direct dispersion of dried CNFs in castor oil.

Ultralight Cellulose-Derived Carbon Nanofibers from Freeze-Drying Emulsion Towards Superior Microwave Absorption

Carbon nanofibers (CNFs) are usually prepared by the carbonization of cellulose aerogels obtained from freeze-drying. However, cellulose with low concentration (below 1 wt%) is required to maintain the good porosity of the aerogels due to the strong hydrogen bonding between the cellulose molecules. In order to address this problem, here, ultralight cellulose-derived CNFs have been fabricated by freeze-drying cyclohexane (CHE)/cellulose nanofiber emulsions and carbonization. Field emission scanning electron microscopy, Raman spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and Fourier transform infrared spectroscopy are used to characterize the resulting CNFs. It is found that the CNFs consist of three-dimensional carbon networks, whose microstructure is easily adjusted by changing the CHE ratio (from 0 to 25 vol%) in the emulsions. The CNFs with high porosity are attributed to the fact that CHE as the oil phase can effectively weaken the hydrogen bonding and reduce the aggregation of the cellulose nanofibers. Carbon lattice defects and residual oxygen-containing functional groups are regarded as polarization centers, leading to the enhancement of dielectric loss. The conductive carbon networks also improve the conductive loss. All these factors improve the microwave absorption performance of the CNFs. So, the produced CNFs exhibit a superior electromagnetic wave performance with a minimum reflection loss of −42.18 dB and effective absorption bandwidth up to 4.9 GHz at 2 mm with a filling ratio of 2 wt%. This work provides a simple, low-cost, and sustainable synthesis route for CNFs used for ultralight high-performance microwave absorption materials.

Low-Cost Hyperelastic Fuller-Dome-Structured Nanocellulose Aerogels by Dual Templates for Personal Thermal Management.

It is critically important to maintain the body's thermal comfort for human beings in extremely cold environments. Cellulose nanofibers (CNF)-based aerogels represent a promising sustainable material for body's heat retention because of their renewability and low thermal conductivity. However, CNF-based aerogels often suffer high production costs due to expensive CNF, poor elasticity and/or unsatisfactory thermal insulation owing to improper microstructure design. Here, a facile dual-template strategy is reported to prepare a low-cost, hyperelastic, superhydrophobic Fuller-dome-structured CNF aerogel (CNF@PU) with low thermal conductivity. The combination of air template by foaming process and ice template enables the formation of a dome-like microstructure of CNF@PU aerogel, in which CNF serves as rope bars while inexpensive polyurethane (PU) acts as joints. The aerogel combines ultra-elasticity, low thermal conductivity (24mW m-1 K-1), and low costs. The as-prepared CNF@PU aerogel demonstrates much better heat retention than commercial thermal retention fillers (e.g., Flannelette and goose down), promising its great commercial potential for massively producing warming garments. This work provides a facile approach for creating high-performance aerogels with tailored microstructure for effective personal thermal management.

Characterization of MSC Growth, Differentiation, and EV Production in CNF Hydrogels Under Static and Dynamic Cultures in Hypoxic and Normoxic Conditions.

Mesenchymal stem cells (MSCs) hold immense therapeutic potential due to their regenerative and immunomodulatory properties. However, to utilize this potential, it is crucial to optimize their in vitro cultivation conditions. Three-dimensional (3D) culture methods using cell-laden hydrogels aim to mimic the physiological microenvironment in vitro, thus preserving MSC biological functionalities. Cellulosic hydrogels are particularly promising due to their biocompatibility, sustainability, and tunability in terms of chemical, morphological, and mechanical properties. This study investigated the impact of (1) two physical crosslinking scenarios for hydrogels derived from anionic cellulose nanofibers (to-CNF) used to encapsulate adipose-derived MSCs (adMSCs) and (2) physiological culture conditions on the in vitro proliferation, differentiation, and extracellular vesicle (EV) production of these adMSCs. The results revealed that additional Ca2+-mediated crosslinking, intended to complement the self-assembly and gelation of aqueous to-CNF in the adMSC cultivation medium, adversely affected both the mechanical properties of the hydrogel spheres and the growth of the encapsulated cells. However, cultivation under dynamic and hypoxic conditions significantly improved the proliferation and differentiation of the encapsulated adMSCs. Furthermore, it was demonstrated that the adMSCs in the CNF hydrogel spheres exhibited potential for scalable EV production with potent immunosuppressive capacities in a bioreactor system. These findings underscore the importance of physiological culture conditions and the suitability of cellulosic materials for enhancing the therapeutic potential of MSCs. Overall, this study provides valuable insights for optimizing the in vitro cultivation of MSCs for various applications, including tissue engineering, drug testing, and EV-based therapies.

Use of nanocelluloses from orange peel and ZnO as hybrid nanofiller in developing functionalized starch nanocomposite for edible coatings

AbstractThis study explores the formulations of orange peel nanocelluloses (NC) with tailored dimensions for the development of functionalized nanocomposites coatings on green chilies. In the present century, the valorization of agro‐waste, specifically orange peel for developing NC facilitated sustainable packaging such as edible films and coatings with improved properties has received importance. As, this approach aligns with the sustainable development goals, including reduced food waste and agro waste. For the work, the derived orange peel celluloses were acid hydrolyzed using sulfuric acid (H2SO4) and hydrochloric acid (HCl) to deliver cellulose nanofibers (CNF) and cellulose nanoparticles (CNP), respectively. The fabricated CNP and CNF were characterized using Fourier transform infrared spectroscopy (FTIR), field emission scanning electron microscopy (FESEM), and thermogravimetric analysis (TGA). The FESEM morphology showed the formation of CNP with diameter ranges from 42.4 to 108 nm and formation of CNF with diameter ranged from 27.4 to 50.5 nm. The creation of the functionalized nanocomposite was done by reinforcing with hybrid nanofillers consisting CNF, CNP consecutively with ZnO in corn starch for tailormade packaging properties in terms of mechanical, physicochemical, optical, thermal properties, and so on. The results reveal improved tensile strength, and reduced water vapor transmission rates of nanocomposite with the addition of hybrid nanofillers. Additionally, green chilies were coated with the functionalized nanocomposites prepared by different concentrations of nanofillers. The storage analysis was performed in terms of weight loss, total chlorophyll content, and microbiological analysis. The developed coatings were found to be effective in extending the shelf life of green chilies. The control samples showed significantly higher weight loss compared to coated ones. The coated samples showed significantly better firmness and total chlorophyll content after 20 days of storage. In comparison to other coatings, NC and ZnO incorporated starch‐based coating was found to be the most effective in maintaining the quality of fresh green chilies throughout the storage. Thus, incorporating NC and ZnO in starch‐based films and coatings presents a promising avenue for sustainable packaging and preservation.Highlights Agro‐waste orange peel was valorized to develop sustainable food packaging. Orange peel‐based nanocellulose was developed using H2SO4 and HCl. Nanocomposite film was developed using hybrid nanofillers. Nanocomposites provide tailored properties due to the nanofillers. Developed nanocomposite was used as edible coatings on green chilies.

Effect of catalyst and oxidant concentrations in a TEMPO oxidation system on the production of cellulose nanofibers.

In traditional TEMPO oxidation systems, the high cost of TEMPO catalysts has been a significant barrier to the industrialization of oxidized CNF. From an economic perspective, presenting the characteristics of various CNFs produced with the oxidation systems with reduced catalyst usage could facilitate the industrial application of CNF across a wide range of fields. In this study, it was demonstrated that reducing the amount of TEMPO catalyst used (from 0.1 to 0.05 mmol g-1) in a conventional oxidation system increased the carboxylate content by approximately 6.3%. Furthermore, the activation of hydroxyl amine TEMPO, which is generated after the oxidation reaction of cellulose, was enhanced by adjusting the dosage of the inexpensive oxidant NaClO, leading to a 20% improvement in carboxylate content. This suggests that controlling the amount of NaClO as an oxidant can be a key parameter in adjusting the dosage of TEMPO to achieve the targeted degree of surface substitution. Results from the dispersion stability, UV-transmittance, and morphological properties of TEMPO-oxidized CNF using microfluidizing treatment showed that high carboxylate content plays a crucial role in producing high-purity CNF suspensions, which are small, uniform, and free from microfibers. Additionally, by varying the number of mechanical treatments applied to the oxidized cellulose, various types of CNF suspensions with different mean widths were obtained. We expect that these findings offer meaningful insights to end-users seeking a breakthrough in the performance limitations of final applications using cellulose nanomaterials.

Ionic liquid reinforced cellulose nanofiber with iron oxide electrocatalyst

Increased attention has been focused on the preparation of nanoarchitectures for applicability in energy, environmental and biological streams. However, concerns have been raised regarding environmental effects due to the harsh chemicals used in such preparations. To overcome this issue, the present study reports the use of a green solvent, 1-methyl-3-propyl-1H-imidazol-3-ium iodide or [Pmim]I, for the preparation of cellulose nanofiber-iron oxide (CNF-Fe2O3) composite. The as-prepared nanofiber composite is characterized with the aid of analytical tools such as X-ray diffraction (XRD), Fourier-transform infrared (FTIR) spectroscopy, field-emission scanning electron microscopy/energy dispersive X-ray spectroscopy (FE-SEM/EDX), and X-ray photoelectron spectroscopy (XPS). As a proof-of-concept demonstration, the resulting nanostructure is employed as an electrocatalyst and is compared with the bare CNFs, non-cellulose NFs and a standard RuO2 catalyst. The results indicate that the CNF-Fe2O3 composite achieves a standard current density (j) of 10 mA cm−2 at only 260 mV compared to 280, 290, and 370 mV for the standard RuO2, the bare CNFs, and non-cellulose nanofibers (NFs), respectively. These differences become more prominent at a high current density of 100 mA cm−2, where the CNF-Fe2O3 requires only 310 mV, while the CNFs, RuO2, and NFs consume 360, 370, and 550 mV, respectively.

Effects of nanosilica and nanocellulose on poly(butylene adipate‐co‐terephthalate) nanocomposites for food packaging applications

AbstractPolymeric materials are highlighted in the global market due to their low cost, excellent properties, and diversity of applications, such as food packaging, which in addition to protecting packaged foods also promotes control and conservation against contaminants. Thus, the objective of this research is to investigate the effects of adding silica nanoparticles and cellulose nanofibers, alone and together, on the properties of poly(butylene adipate‐co‐terephthalate), aiming for application in food packaging. For this purpose, PBAT and the nanofillers were initially mixed in a rheometer to produce masterbatches, and, then, to be processed by a single screw extruder to generate the nanocomposites. The nanocomposites are analyzed by scanning electron microscopy, x‐ray diffraction, thermogravimetric analysis, differential scanning calorimetry, nuclear magnetic resonance, tensile testing, water contact angle, and microbial permeability. In low concentrations, it is observed that the system tends to be less heterogeneous. Nanoparticles do not interfere with thermal stability and present a barrier to microorganisms. Interestingly, in the two conditions studied, polymers with cellulose nanofibers or silica nanoparticles have filtering capacity, being effective as physical barriers to the growth of microorganisms within 60 days. However, the effect on mechanical properties is small, being more pronounced with the use of cellulose nanofibers.

Production of Cellulose Nanofibers From Pineapple Peel (Ananas comosus) and Application in Biodegradable Films

AbstractThe waste of pineapple (Ananas comosus) juice accounts for 35% of the fruit's weight, and this organic material is rich in fibers and cellulose, making it a promising source for producing new ingredients for biodegradable packaging. This study objected to cellulose‐produced nanofibers from pineapple peel by chemical and enzymatic treatment combined with mechanical treatment and subsequently evaluated the application of these nanofibers as a reinforcing agent in biodegradable films. The cellulose nanofibers produced through enzymatic treatment with a sonicator presented the best results and were applied in biodegradable films at concentrations of 3% and 6%. The addition of 6% of cellulose nanofibers increased the tension (26.01 ± 0.78). It reduced the elongation percentage (3.27 ± 0.38) of films in addition to expanding the biodegradability, with up to 96% degradation observed after just 1 day. The use of nanofibers obtained from pineapple peel is a promising ingredient for the development of biodegradable packaging.

CO2 foam structure and displacement dynamics in a Hele–Shaw cell

The substitution of CO2 gas with CO2 foam for improved mobility control has recently attracted research attentions in enhanced oil recovery (EOR) as well as aquifer and soil remediation. However, the interplay between CO2 foam properties and oil displacement remains less investigated. In this work, using clear visualizations, we systematically investigate the dynamic advection-dominated foam morphology, its corresponding viscosity, and the efficiency and dynamics of oil displacement process by CO2 foam in a Hele–Shaw cell under the effects of gas ratio (Rg), fluid injection rates (Qt), and surfactant type. Clear visualization enables particle image velocimetry to calculate actual, rather than nominal, foam velocity that significantly affects the estimated foam viscosity. Our results demonstrate that at elevated gas ratios under constant total injection rate, larger and more uniform bubbles with less number density and greater interfacial area are obtained. Increasing the injection rates leads to finer foam texture at a constant gas ratio. Different foam structures have an impact on the foam viscosity, with a general increasing trend of viscosity for larger bubbles as Rg increases from 0.5 to 0.85. The higher the foam viscosity, the more stable displacement interfaces with less viscous fingers are observed, leading to improved sweeping rates. The green surfactants (saponin + Cellulose NanoFibers) provide foams with higher viscosity and, thus, more stable displacement interfaces. These findings highlight the important effect of Rg–dependent foam structure on its viscosity, which in turn is crucial for controlling the mobility of CO2 foam to maximize oil recovery rate during EOR processes.

Bio-Templated Aerogel Fibers: Heterogeneous Spinodal Architecting and In Situ Fibrillation of Thermoplastic Polyurethane-Silica on Nanostructured Cellulose Nanofiber Scaffold for Enhanced Thermomechanical Performance.

This study addresses the inherent fragility and fractal limitations of traditional silica aerogels by developing a bio-templated aerogel fiber. Integrating cellulose nanofibers (CNFs), thermoplastic polyurethane (TPU), and silica aerogel (SA) in a dimethyl sulfoxide (DMSO) dispersion, a gel-spinning technique was employed to create aerogel fibers with superior thermomechanical performance. CNF also provided excellent rheological modification for successful spinnability, fast gelation, and fiber formation. The unique hierarchical structure of these fibers, formed through hot-stretching and surface modification, combined the superior mechanical strength and flexibility of TPU with the exceptional insulation properties of CNF and SA. The CNF network, encapsulated within the SA particles, formed a core-shell structure, axially aligned, that significantly enhances the thermal stability and mechanical performance of the fibers while maintaining a lightweight and porous architecture. Comprehensive morphological, thermal, and mechanical analyses were conducted to evaluate the properties of the developed aerogel fibers. Fourier transform infrared (FTIR) spectroscopy and nuclear magnetic resonance (NMR) spectroscopy verified the successful surface modification and grafting reactions on CNF, contributing to improved hydrophobicity and thermal insulation. Adjusting the CNF content allowed for tailoring of the thermomechanical characteristics, with a notable 294% increase in tensile strength from 5.3 to 15.6 MPa and an enhanced crystallization temperature from 106 to 119.97 °C. Furthermore, cyclic tensile and compression tests validated the durability and shape recovery capabilities of the aerogel fibers, making them promising candidates for high-performance applications in extreme environments. The thermal conductivity validated by experimental data further highlights the potential of CNF-based aerogel fibers as sustainable and multifunctional materials for advanced thermal insulation, mechanical reinforcement, and flexible structural applications.