Search Results (703)

To tackle the poor emulsibility of hydrophilic cellulose nanocrystals (CNCs), this study prepared octenyl succinic anhydride (OSA)-modified bamboo shoot CNC (OSNC) via acid hydrolysis and esterification, using microcrystalline cellulose (MCC) as a control. The degree of substitution (DS), chemical structure, crystalline structure, morphological characteristics, zeta potential, wettability, and thermal stability of OSNC and OSA-modified MCC (OSA-MCC) were characterized using multiple techniques. Results showed that at the optimal cellulose-to-OSA ratio (1:0.225), OSNC had a higher DS (0.029 ± 0.01) than OSA-MCC (0.024 ± 0.02). FTIR confirmed successful OSA grafting; XRD showed a preserved cellulose I crystal form with slightly reduced crystallinity; OSNC had improved dispersion stability (zeta potential: −44.0 mV), balanced amphiphilicity (contact angle: 61.8°), and enhanced thermal stability. This work enables high-value utilization of bamboo shoot by-products and supports developing green food-grade cellulose-based nanomaterials for food emulsions. Full article

The removal of cationic dyes from industrial wastewater presents a significant environmental challenge. This research examines the effectiveness of functionalized cellulose-based silica aerogels as sustainable adsorbents for methylene blue (MB) dye. This research provides a systematic comparative study on the effectiveness of four distinct functionalization strategies, carboxylate (CCNC), double carboxylate (DCCNC), carboxymethyl (CMC), and thiol-modification, applied to cellulose-based silica aerogels as sustainable adsorbents for methylene blue (MB) dye. Cellulose nanocrystals (CNCs) were extracted from sugarcane bagasse waste and subsequently functionalized into carboxylate (CCNC), double carboxylate (DCCNC), carboxymethyl (CMC), and thiol-modified variants. The materials were later integrated into a silica matrix, resulting in the formation of porous aerogel nanocomposites. The materials underwent thorough characterization through FTIR, XRD, SEM, TGA, and BET analyses, validating successful functionalization and the development of mesoporous structures. Batch adsorption tests demonstrated that the CMC-silica aerogel exhibited superior performance, attaining a maximum adsorption capacity of 197 mg/g and complete removal efficiency under ideal circumstances (pH 10, 25 °C, 60 min). The adsorption process is accurately characterized by the Langmuir isotherm and pseudo-second-order kinetic models, signifying monolayer adsorption and chemisorption as the rate-limiting step. The thermodynamic parameters indicate that the adsorption process is exothermic and spontaneous. The CMC-silica aerogel exhibited significant reusability, maintaining over 90% efficiency after six consecutive cycles. The findings illustrate the efficacy of functionalized cellulose–silica aerogels, especially the CMC form, as effective, environmentally sustainable, and reusable adsorbents for the treatment of dye-polluted water. Full article

In this work, nanofibers and cellulose nanocrystals from the native Amazonian bamboo Guadua weberbabeuri were used in structural cementitious composites. Through the preparation of bamboo nanofibers—bleached cellulose pulp (BCP) and cellulose nanocrystals (CNC), as well as obtaining shredded bamboo (SB) and delignified cellulose pulp (DCP)—the additions corresponding to the additive nanomaterials were characterized with physical tests such as water absorption, specific mass, void index, and dimensional variation. A mechanical tensile strength test was carried out at 28 days, with an incorporation content of 0.40% of mass in relation to the cement. The results indicated, in relation to the control, improvement in the physical properties, especially in the additions with nanofibers and cellulose nanocrystals. For the mechanical tensile strength tests, the indicator allowed an increase of 14.60% with the addition of nanofibers and 12.70% in the addition of nanocrystals. Therefore, with the execution carried out, it could be seen that the incorporation was able to generate optimization in the joint performance of the materials under analysis, reinforcing the practices and ideals arising from civil engineering, nanotechnology, and sustainability. Full article

Bioplastics are plastics derived from natural resources like corn starch, biomass, sugarcane bagasse, and food waste. Unlike fossil-fuel-based plastics, they are entirely or partially bio-degradable. Cellulose- and starch-based bioplastics are already used for applications like packaging, cutlery, bowls, straws, and shopping bags. With the aim of developing eco-friendly biofilms for various applications, cellulose nanocrystals (CNCs) were obtained by sulfuric acid hydrolysis of waste cellulose and functionalized by transesterification with exhausted oils. The resulting transesterified nanocellulose (TCNC) was used as a reinforced material of PLA at different concentrations to develop biofilms using the solvent casting method. The biofilms composed of PLA and TCNC were assessed through Fourier-transform infrared spectroscopy (FTIR), mechanical properties, moisture barrier property (water vapor permeability rate—WVTR), and measurements of the water contact angle (WCA). A scanning electron microscopy (SEM) analysis confirmed the high compatibility of the PLA blended with TCNC at 1% and 3%. The inclusion of transesterified cellulose nanocrystals (TCNCs) to PLA increased the hydrophobicity, the film tensile strength, and the water vapor barrier properties of the final composite films. Full article

Açaí, a berry emblematic of Amazonian biodiversity, is a major Brazilian product whose market value is largely concentrated in its pulp, leaving the residual biomass—particularly the fibrous seed—underexploited and typically discarded in landfills, with negative environmental and social consequences. To address this gap, this study employs a systematic technology roadmapping approach, integrating bibliometric analysis, patent landscaping, and expert consultations to consolidate fragmented data. This methodology enables the mapping of innovation trajectories across technology readiness levels, product categories, market segments, and key stakeholders. The roadmap identifies emerging trends and opportunity windows for valorizing açaí biomass via integrated biorefinery approaches, moving beyond traditional low-complexity uses such as thermal energy and seed-derived coffee substitutes. The highlighted products include pharmaceutical extracts, cosmetic ingredients, nanopapers, and cellulose nanocrystals, leveraging the biomass’s biochemical composition, notably antioxidants, mannose, and inulin. This methodological framework facilitates a dynamic analysis of technological maturation and market evolution, offering strategic insights to guide industrial investments and policy development. Findings indicate that biorefinery integration enhances resource efficiency and product diversification, situating açaí biomass valorization within broader bioeconomy strategies. The study demonstrates the efficacy of technology roadmapping in structuring prospective innovation pathways and in supporting the sustainable utilization of the Amazonian biomass. Full article

Exhibiting significant potential for sustainable packaging due to their renewability and biodegradability, soy protein isolate (SPI) films are nevertheless critically hampered by inherent brittleness, poor water resistance, and a lack of bioactivity. Herein, we demonstrate a hierarchical multi-network strategy that transforms SPI into a high-performance, functional biocomposite. A robust covalent backbone was forged via Schiff base cross-linking between SPI and dialdehyde cellulose nanocrystals (DACNCs) derived from agricultural biomass, while proanthocyanidins (PAs) were strategically incorporated to create a secondary, pervasive hydrogen-bonding network. This hierarchical architecture effectively overcomes the typical trade-offs between mechanical strength and functionality seen in singly modified biopolymers, unlocking a suite of remarkable performance enhancements. The optimized film exhibited a 491% increase in tensile strength (to 15.54 MPa) and elevated thermal stability to 330 °C. Critically, the film was endowed with potent functionalities, including complete UV-blocking, high antioxidant capacity (93.2% ABTS scavenging), and strong, broad-spectrum antimicrobial activity. The film’s practical efficacy was validated in a preservation test, where the coating extended blueberry shelf life by inhibiting fungal spoilage and reducing weight loss by nearly 30% relative to uncoated controls after 15 days of storage. This work provides a powerful framework for developing advanced biocomposites with tailored properties for active food packaging and beyond. Full article

Cellulose nanocrystals (CNCs) have been extensively studied for their ability to maintain liquid crystal (LC) order within solid films, providing a robust template for the self-assembly of plasmonic nanorods (NRs) and the construction of nanostructures. The self-assembly mechanism of NRs combined with uniaxially nematic CNC LCs has long attracted considerable attention. In this study, we investigated the influence of pH and aspect ratio on the self-assembly of composite NR–uniaxial nematic CNC systems. The phase diagram indicates that the uniaxial nematic phase of CNCs becomes more stable at higher pH, while it is more sensitive to disturbance from NRs with smaller aspect ratios. Furthermore, a composite effective excluded volume model was developed, in which the interaction between NRs and CNCs is incorporated, and the effective excluded volume is governed by both the effective CNC diameter and the NR aspect ratio. This study elucidates the influence mechanism of pH and aspect ratio on the self-assembly of composite NR–uniaxial nematic CNC systems, in good agreement with experimental observations. Our results provide fundamental insights into the utilization of uniaxial nematic CNC LCs as templates for fabricating novel nanomaterials and nanostructures, and deepen understanding of the mechanisms governing such composites. Full article

Heavy metal contamination in water, predominantly from copper (Cu(II)) ions, poses substantial risks to human and environmental health. This study developed a novel, robust adsorbent known as a carboxylate cellulose nanocrystal–silica–graphene oxide hybrid composite porous monolith, which effectively removes Cu(II) from water in a rapid manner. Carboxylate cellulose nanocrystals with enhanced metal-binding properties were synthesized from cellulose extracted from sugarcane bagasse, a significant agricultural byproduct. The porous monolith was synthesized through the combination of carboxylate cellulose nanocrystals, tetraethyl orthosilicate (TEOS), and graphene oxide, utilizing a sol–gel method. The efficacy of the synthesis was confirmed using Fourier-Transform Infra-red (FTIR), X-ray diffraction (XRD), thermogravimetric analysis (TGA), scanning electron microscope (SEM), and Brunauer–Emmett–Teller (BET) analyses. The material exhibited a highly porous mesoporous structure with a surface area of 512 m²/g, signifying a significant enhancement. Batch adsorption experiments under optimal conditions (pH = 5.5, contact time = 240 min, initial concentration = 200 mg/L) demonstrated a high experimental adsorption capacity of 172 mg/g for Cu(II). The adsorption process was best described by the Langmuir isotherm model, which yielded a theoretical maximum capacity (q_m) of 172 mg/g, and the pseudo-second-order kinetic model, confirming monolayer coverage and chemisorption as the rate-limiting step. Thermodynamic analyses demonstrate that the process is both spontaneous and exothermic. The porous monolith demonstrates the capability for multiple uses, maintaining over 70% efficiency after five cycles. The findings indicate that the carboxylate cellulose nanocrystal–silica–graphene oxide hybrid composite porous monolith is an efficient and robust method for the remediation of copper-contaminated water. Full article

The insistent presence of detrimental chemical dyes, such as methylene blue (MB), in aquatic ecosystems creates a significant environmental fear that requires the development of innovative and effective remediation methods. This study examines the production and application of a novel carboxylate cellulose nanocrystal-silica-titanium dioxide (CCNC-silica-TiO₂) hybrid composite aerogel designed to enhance the photocatalytic degradation of methylene blue (MB). Carboxylic groups were incorporated into cellulose nanocrystals (CNCs) derived from sugarcane bagasse (SCB) waste to improve their dye adsorption capacity. The CCNCs were later incorporated into a silica aerogel matrix using a sol–gel method, followed by the introduction of TiO₂ nanoparticles. Characterization techniques, including FTIR and XRD, confirmed the successful chemical functionalization and composite synthesis. SEM analysis revealed a highly porous three-dimensional architecture, whilst BET surface area assessment showed that the CCNC-SiO₂-TiO₂ aerogel possessed a significant specific surface area of 448.69 m²/g. Under ultraviolet light, the hybrid aerogel demonstrated remarkable photocatalytic performance, achieving a 93% degradation rate of methylene blue, far above the 22% recorded in a CCNC-silica control. The degradation kinetics followed a pseudo-first-order model. The composite demonstrated significant reusability, maintaining over 70% efficiency after five consecutive cycles. The findings indicate that the adsorptive capacity of carboxylate CNCs, together with the photocatalytic efficiency of TiO₂, improves the efficacy, stability, and longevity of the CCNC-SiO₂-TiO₂ aerogel in wastewater treatment. Full article

Hydrogels comprise three-dimensional networks of hydrophilic polymers and have attracted considerable interest in various sectors, including the biomedical, pharmaceutical, agricultural, and food industries. These materials offer significant benefits for food packaging applications, such as high mechanical strength and excellent water absorption capacity, thereby contributing to the extension of product shelf life. Therefore, the aim of this study is to compare the performance of citric acid and glutaraldehyde as crosslinking agents in gelatine-based hydrogels reinforced with cellulose nanocrystals (CNC), contributing to the development of safe and environmentally responsible materials. The hydrogels were prepared using the casting method and characterised in terms of their physical, mechanical, and structural properties. The results indicated that hydrogels crosslinked with glutaraldehyde exhibited higher opacity, lower transparency, and greater mechanical strength, whereas those crosslinked with citric acid demonstrated improved clarity, reduced water permeability, and enhanced swelling capacity. The incorporation of CNC further improved mechanical strength, reduced weight loss, and altered both surface homogeneity and optical properties. Microstructural results obtained by SEM were consistent with the mechanical properties evaluated (TS, %E, and EM). The Gel-ca hydrogel displayed the highest elongation value (98%), reflecting better cohesion within the polymeric matrix. In contrast, films incorporating CNC exhibited greater roughness and cracking, which correlated with increased rigidity and mechanical strength, as evidenced by the high Young’s modulus (420 MPa in Gel-ga-CNC2). These findings suggest that the heterogeneity and porosity induced by CNC limit the mobility of polymer chains, resulting in less flexible and more rigid structures. Additionally, the DSC analysis revealed that gelatine hydrogels did not exhibit a well-defined Tg, due to the predominance of crystalline domains. Systems crosslinked with citric acid showed greater thermal stability (higher Tm and ΔH_m values), while those crosslinked with glutaraldehyde, although mechanically stronger, exhibited lower thermal stability. These results confirm the decisive effect of the crosslinking agent and CNC incorporation on the structural and thermal behaviour of hydrogels. In this context, the application of hydrogels in packaged products represents an eco-friendly alternative that enhances product presentation. This research supports the reduction in plastic consumption whilst promoting the principles of a circular economy and facilitating the development of materials with lower environmental impact. Full article

This study introduces an efficient, all-aqueous emulsion-templating strategy for fabricating highly tunable yeast immobilization carriers with superior biocatalytic performance. Utilizing cellulose nanocrystals (CNCs) to stabilize dextran/polyethylene glycol (Dex/PEG) water-in-water emulsions, an architecture-controlled void is obtained by crosslinking the PEG-rich phase with variable concentrations of polyethylene glycol diacrylate (PEGDA) (10–25 wt%). This approach successfully yielded macroporous networks, enabling precise tuning of void diameters from 10.4 to 6.6 μm and interconnected pores from 2.2 to 1.4 μm. The optimally designed carrier, synthesized with 15 wt% PEGDA, featured 9.6 μm voids and robust mechanical strength (0.82 MPa), and facilitated highly efficient yeast encapsulation (~100%). The immobilized yeast demonstrated exceptional fermentation activity, remarkable storage stability (maintaining > 95% productivity after 4 weeks), and high reusability (85% activity retention after seven cycles). These enhancements are attributed to the material’s excellent water retention capacity and the provision of a stable microenvironment. This green and straightforward method represents a significant advance in industrial cell immobilization, offering unparalleled operational stability, protection, and design flexibility. Full article

This study demonstrates the valorization of orange peel waste as a sustainable feedstock for the production of cellulose nanocrystals (CNCs). Compositional analysis revealed a cellulose content up to 10.0% in the raw material. After performing the alkaline/peroxide treatment, CNCs were isolated via acid hydrolysis. Different inorganic acids were compared, namely sulfuric, phosphoric, and hydrochloric acids at low molar concentrations. The resulting CNCs showed distinct morphological and physicochemical properties, with sulfuric acid treatment yielding the highest crystallinity index (TCI) of 0.86 under conditions of 3.0 mol/L, 80 °C, and 225 min. Additionally, the presence of sulfate or phosphate groups significantly influenced the thermal degradation behavior and the inorganic residue content in the obtained CNCs. Finally, the CNCs were successfully tested as co-initiator for lactide ring-opening polymerization. The results show that the molecular weights of the resulting polylactide varied depending on the CNC dispersion. This work supports the use of orange peel waste as a bio-source for CNC production and their potential application as a co-initiator in the synthesis of polyesters. Full article

The viscous rheological behavior of suspensions of mixtures of fumed silica nanoparticles (N20) and rod-shaped cellulose nanocrystals (NCC) were studied experimentally. The fumed silica concentration varied from 2 to 11.3 wt% and the NCC concentration varied from 0.99 to 6.73 wt%. The suspensions of pure fumed silica, pure NCC, and mixtures of N20 and NCC were non-Newtonian shear-thinning in nature. The viscosity versus shear rate data of all suspensions of pure and mixed additives could be described satisfactorily by a power-law model. The consistency and flow behavior indices of the suspensions were strongly dependent on the concentrations of both N20 and NCC. While the consistency index increased sharply with the increases in additive (N20 and NCC) concentrations, the flow behavior index generally decreased with the increases in N20 and NCC concentrations. Thus, the suspensions became more shear-thinning with the increases in N20 and NCC concentrations. The shear-thinning of suspensions was due to two different mechanisms: the orientation of rod-shaped cellulose nanocrystals in the flow direction with the increase in shear rate and the break-up of large agglomerates of fumed silica aggregates with the increase in shear rate. Full article

Phosphorylated cellulose nanocrystals (P-CNCs) are a superior alternative to conventional sulfuric acid-derived CNCs because of their enhanced thermal and colloidal stability. However, further research is needed to understand the factors influencing their synthesis and properties for advanced material applications. In this study, P-CNCs were synthesized from bleached hardwood kraft pulp (BEKP) using a controlled hydrolysis method involving pretreatment with H₃PO₄ followed by reaction with metaphosphoric acid (HPO₃) and urea. To optimize the process, a full factorial design was employed to evaluate the effects of reaction time (60–90 min) and HPO₃ concentration (3–4 M). The P-CNCs were characterized using physicochemical, morphological, and thermal analyses. Surface charge densities ranged from 757 to 1993 mmol/kg, with exceptional colloidal stability, as evidenced by zeta potentials ranging from −30.17 to −67.40 mV. Statistical analysis showed that reaction time had a significant main effect on surface charge (p-value = 0.0022) and zeta potential (p-value = 0.0448), while a significant interaction between reaction time and HPO₃ concentration was observed when analyzing the surface charge (p-value = 0.0097), suggesting a combined effect of these factors on the surface modification of CNC. Crystallinity indices ranged from 63.6% to 71.3%, and the thermal stability exceeded that of the raw material. These findings contribute to a better understanding of the surface modification and stability of P-CNCs and support efforts to sustainably produce functional CNCs for advanced composite applications. Full article

This study proposes a novel approach for preparing a laminated carbides and nitrides (MXene) membrane with loose nanochannels by intercalating cellulose nanocrystal (CNC) and cross-linking with glutaraldehyde. The interlayer spacing of the MXene membrane can be expanded by one-dimensional CNC, while cross-linking with glutaraldehyde enhances the stability of the membrane. The optimized membrane displays a high water permeate flux of 96.8 L m⁻² h⁻¹ (2.1 times higher than MXene membrane) and good selectivity (methyl blue rejection rate: ~99.6%; NaCl rejection rate: <5.0%). This strategy provides a universal way to prepare high-performance two-dimensional membranes. Full article