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In this study, significant improvements in mechanical properties have been seen through the efficient inclusion of Oil Palm Cellulose Nanofibrils (CNF) as nano-fillers into green polymer matrices produced from biomass with a 28 % carbon content. The goal of the research was to make green epoxy nanocomposites utilizing solution blending process with acetone as the solvent with the different CNF loadings (0.1, 0.25, and 0.5 wt%). An ultrasonic bath was used in conjunction with mechanical stirring to guarantee that CNF was effectively dispersed throughout the green epoxy. The resultant nanocomposites underwent thorough evaluation, comparing them to unfilled green epoxy and evaluating their morphological, mechanical, and thermal behavior using a variety of instruments. Field-emission scanning electron microscopy (FE-SEM) was used to validate findings, which showed that the CNF were dispersed optimally inside the nanocomposites. The thermal degradation temperature (Td) of the nanocomposites showed a marginal decrement of 0.8 % in temperatures (from 348 °C to 345 °C), between unfilled green epoxy (neat) and 0.1 wt% of CNF loading. The mechanical test results, which showed a 13.3 % improvement in hardness and a 6.45 % rise in tensile strength when compared to unfilled green epoxy, were in line with previously published research. Overall, the outcomes showed that green nanocomposites have significantly improved in performance., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

The development of high-strength and intrinsic flame-retardant natural fiber-reinforced green composite (NFRGC) is a landmark for high-performance structural applications. This paper reports a biobased, high-performance, flame-retardant composite material based on diverse bio-resources. Tough and strong cellulose long filaments (CLFs) are combined with vanillin-derived epoxy (VDE) resin to achieve high strength and flame-retardant NFRGC. The green composite was fabricated using a simple hand lay-up and compression molding technique. The green composite showed a noteworthy increment of 100.9 % flexural strength and 346 % flexural modulus compared to the neat VDE resin. Interestingly, despite the highly flammable nature of CLF, the green composite passes a V-0 rating under the UL-94 test, indicating excellent flame-retardant characteristics. Additionally, the green composite demonstrated outstanding hydrophobicity with a water contact angle of 104.2° and good chemical stability in various acidic and organic solvents. The green composite's excellent mechanical and physical properties show its potential for high-strength and flame-retardant structural applications., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that have influenced the study reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

Cellulose, as a biomass resource, has attracted increasingly attention and extensive research by virtue of its widely sources, ideal degradability, good mechanical properties and easy modification due to its rich hydroxyl groups. Nevertheless, it is still a challenge to attain high performance cellulose-based composite film materials with diverse functional combinations. In this work, we developed a multifunctional cellulose-based film via a facile impregnation-curing strategy. Here, benzoxazine resin (BR) is used as an optically functional component to endow the microfibrillated cellulose (MFC) film with powerful light management capabilities including UV and blue light double shielding, high transmittance, and high haze. Meanwhile, the introduction of tannic acid (TA) substantially enhanced the mechanical properties of the film, including tensile strength and toughness, by constructing energy-sacrificial bonds. An effective self-healing of the film was achieved by controlling the degree of BR curing. The final films exhibited 98.24 % UV shielding and 89.98 % blue light blocking, good mechanical properties including a tensile strength of 202.21 MPa and tensile strain of 7.1 %, as well as desirable thermal healing properties supported by incompletely cured BR. This work may provide new insights into the high-value utilization of biomass resources. [ABSTRACT FROM AUTHOR]

Micro-to-nano transformation can make a material unique. This research uses jute microfiber to extract Holo and Alpha forms of cellulose, which are later attempted to electrospun into superfine nanofibers (NFs). Initial investigation of morphological, physicochemical, crystallographic, and thermal properties confirmed successful synthesis of Holo and Alpha-cellulose (H/A-cellulose). Afterwards, the electrospinnable concentration of H/A-cellulose was optimized and their bead-free ultrafine NFs in the range of 109–145 nm were fabricated. FTIR analysis confirmed the source composition in Holo and Alpha CNF with the partial formation of trifluoroacetyl esters. Alpha CNF exhibited better structural integrity despite the crystallinity and thermal stability deteriorated in both Holo and Alpha CNF. Both Holo and Alpha CNF exhibited adequate mechanical performance and liquid uptake properties. Alpha CNF showed better morphological stability in organic solvents and slower biodegradation than Holo CNF. Subsequent investigation revealed that both Holo and Alpha CNF didn't exhibit cytotoxic effects on COS-7 cells and above 90 % of cells were viable in contact with both CNF. Significant proliferation and attachment of COS-7 cells were noticed within 7 days of incubation with the prepared CNF. Our findings revealed that jute-extracted cellulose can be a viable and potential source for constructing cellulose-based advanced nano-biomaterials. Graphical representation of the scaffold fabrication. [Display omitted] • Extraction of Holo and Alpha-cellulose from jute fiber • Fabrication of Holo and Alpha CNF via electrospinning • Alpha CNF was more structurally stable than Holo CNF. • Holo CNF and Alpha CNF have adequate surface-wetting and liquid uptake properties. • Both Holo CNF and Alpha CNF were non-toxic against COS-7 cells and favored excellent cell proliferation and attachment. [ABSTRACT FROM AUTHOR]

Poly(vinyl alcohol) (PVA) biocomposite films reinforced with cellulose nanofibrils (CNF) and biologically active tannic acid (TA) were prepared. The influence of different concentrations of CNF and TA in the PVA polymer matrix was investigated in terms of mechanical properties, thermal properties and hydrophobicity improvement of the prepared films. The results showed that in all cases the addition of CNF and TA improved the values of tensile strength and elastic modulus. The PVA film with 10 % CNF exhibited a 30 % higher tensile strength, and the three-component PVA film with 2 % CNF and 10 % TA (P2C10T) exhibited a 40 % higher tensile strength compared to the neat PVA film. The thermal properties (T g , T onset) of the PVA biocomposite films were greatly improved, with a significant effect observed for the three-component PVA films. The T g of the PVA film with 10 % CNF and 10 % TA was 87 °C, 12 °C higher than that of the neat PVA film. For three-component PVA biocomposites with 4 % and 6 % CNF and with all weight percentages of TA, the T onset shifted to a higher temperature range by about 30 °C compared to the neat PVA film. The PVA film with 2 % CNF and 10 % TA exhibited about a 20° higher contact angle than the neat PVA film. Moreover, the addition of both fillers to the PVA matrix resulted in PVA biocomposites with lower water absorption. PVA film with 10 % TA absorbed about 90 % less water and PVA film with 10 % CNF and 10 % TA absorbed about 80 % less water than the neat PVA film after the films were soaked in water for one hour. The better properties of the composite films produced are due to hydrogen and ester bonds between the components of the composite, which was confirmed by FT-IR spectroscopy. Antioxidant effective films were also obtained due to the biologically active TA to the PVA and PVA/CNF systems. [Display omitted] [ABSTRACT FROM AUTHOR]

Hydrogen peroxide combined with acid treatment demonstrates its respective characteristics for the separation of lignocellulosic biomass. Herein, holocellulose was extracted from Cattail leaves (CL) by a two-step treatment with alkali and hydrogen peroxide-acetic acid (HPAA). Then carboxylated nanocellulose was hydrolyzed with a mixed organic/inorganic acid. The chemical composition of the holocellulose and the physicochemical properties of the separated carboxylated nanocellulose were comparable. Carboxyl groups were introduced on the nanocellulose as a result of the esterification process with citric acid (CA), which endows the nanocellulose with high thermal stability (315–318 °C) and good light transmission (>80 %). Furthermore, morphological analyses revealed that nanocellulose had a spider-web-like structure with diameter between 5 and 20 nm. [ABSTRACT FROM AUTHOR]