Search Results (38)

This study investigates the development of biodegradable chitosan-based films as a sustainable alternative to conventional non-biodegradable food packaging materials. Chitosan, a naturally occurring polymer, possesses inherent film-forming ability and biodegradability; however, its limited mechanical and thermal properties constrain its practical applications. In this work, chitosan films were fabricated via compression molding, and their thermo-mechanical performance was systematically evaluated. The incorporation of fillers, such as titanium dioxide and silica, resulted in a 50% enhancement in tensile strength and an 86% improvement in flexibility. Further optimization of dual-filler compositions led to an additional 45% increase in elasticity, demonstrating the potential of synergistic reinforcement. These findings underscore the viability of tailored chitosan composites as high-performance, biodegradable materials for the next generation of sustainable materials. Full article

Agricultural and agro-industrial residues are increasingly recognized as sustainable, low-cost feedstocks for high-performance biomedical materials. This review critically examines the translational potential of polysaccharides, proteins, inorganic compounds, and phytochemical-rich extracts derived from agro-waste, highlighting their chemical features, structure–function relationships, and application-specific readiness. Polysaccharides such as nanocellulose, pectin, and chitosan emerge as the most advanced biopolymer platforms, particularly in wound healing, drug delivery, and 3D-printed scaffolds. Protein-derived materials—including collagen, gelatin, keratin, and soy protein—show strong promise in regenerative medicine, though challenges in mechanical stability and batch reproducibility remain. Inorganic phases such as hydroxyapatite and silica obtained from eggshells, rice husk ash, and marine shells demonstrate high bioactivity, with dental and bone applications approaching clinical translation. Finally, fruit-residue phytochemicals provide multifunctional antioxidant and antimicrobial enhancements to composite systems. By integrating material chemistry, processing strategies, and translational considerations, this review outlines the current state, challenges, and future perspectives for advancing agro-waste-derived biomaterials within a circular bioeconomy. Full article

Energy-efficient buildings require materials with low thermal conductivity, and high fire resistance and mechanical properties. Traditional chitosan aerogel is limited by its poor fire resistance and silica aerogel is either brittle or displays a high thermal conductivity. Herein, we report a dual-modified aerogel with high mechanical properties, low thermal conductivity, and excellent fire resistance. Briefly, the chitosan-derived silica aerogel (CA) was first fabricated, followed by loading varying contents of phytate-piperazine (PPA) intumescent flame-retardant. This well-designed aerogel (CA/PPA) combines with the high mechanical strength of chitosan aerogel, the excellent fire resistance function of silica aerogel, and the intumescent flame-retardant performance of PPA. The as-created CA/PPA-2.0 exhibited enhanced mechanical properties, as evidenced by the fact that its compressive strength rose from 1.3 ± 0.10 to 2.9 ± 0.23 MPa at 90.0% strain compared to that of neat chitosan aerogel. Additionally, compared to CA, the CA/PPA aerogel with 2.0 wt% PPA exhibits significant fire safety performance. For instance, the peak heat release rate, total heat release, maximum average rate of heat emission, and thermal conductivity were reduced by 62.1%, 55.6%, 48.4%, and 12.5%, respectively. In addition, the CA/PPA-2.0 composite aerogel also exhibits a fire-alarm performance under flame attack. This work introduces a feasible strategy to produce high-performance aerogels with promising applications in construction, aerospace, and thermal insulation. Full article

Efficient and selective separation of gallium (Ga(III)) from alkaline industrial waste streams remains a significant challenge due to the coexistence of chemically similar ions such as Al(III) and V(V). In this study, a novel ion-imprinted chitosan-based adsorbent (CS/(H-CGCS)-Ga-IIP) was synthesized via a hybrid cross-linking strategy using glutaraldehyde and siloxane-modified chitosan. The optimized material exhibited a high adsorption capacity of 106.31 mg·g⁻¹ for Ga(III) at pH 9, with fast adsorption kinetics reaching equilibrium within 60 min. Adsorption behavior followed the pseudo-second-order kinetic and Langmuir isotherm models, and thermodynamic analysis indicated a spontaneous and endothermic process. In simulated Bayer mother liquor systems, the material demonstrated outstanding selectivity and a distribution coefficient ratio k_d-Ga/k_d-Al = 146.9, highlighting its strong discrimination ability toward Ga(III). Mechanistic insights from SEM-EDS, FTIR, and XPS analyses revealed that Ga(III) adsorption occurs via electrostatic interaction, ligand coordination, and structural stabilization by the siloxane network. The material maintained good adsorption performance over three regeneration cycles, indicating potential for reuse. These findings suggest that CS/(H-CGCS)-Ga-IIP is a promising candidate for the sustainable recovery of gallium from complex alkaline waste streams such as Bayer process residues. Full article

This work aims to study the catalytic properties of Fe, Cr, and Cu catalysts deposited on chitosan–silica (SBA-15) composites in liquid phase oxidation of cyclohexane (CH) with H₂O₂ and photocatalytic hydrogen evolution reaction. The catalysts were obtained by consecutive adsorption of chitosan (CS) and metal ions (Fe³⁺, Cr³⁺, Cu²⁺) on SBA-15 at ambient conditions. Characterization of the catalysts by XRD, IR spectroscopy, XPS, TEM, SEM, etc., showed the CS and metal ion adsorption on the solid support. Modification with CS provided better immobilization of the metal ions on SBA-15. The synthesized catalysts demonstrated different performance in liquid phase oxidation of cyclohexane with H₂O₂ under mild conditions at 40 °C and atmospheric pressure. Cyclohexane conversion on Fe–CS/SBA-15 (18.5%) and Cr–CS/SBA-15 (21.6%) was higher than on Cu–CS/SBA-15 (9.3%). The influence of different conditions of the reaction such as time, temperature, catalyst dosage, substrate and oxidant ratio on cyclohexane conversion in the presence of the most efficient Cr–CS/SBA-15 catalyst was also studied. The optimal reaction conditions were found to be the following: duration of reaction—4 h, temperature of reaction—50 °C, m_cat—0.03 g, a substrate/H₂O₂ ratio of 1:3. In addition, Cr–CS/SBA-15 and Fe–CS/SBA-15 catalysts were studied in a photocatalytic H₂ evolution reaction. The Fe-containing catalyst demonstrated superior efficiency in photocatalytic H₂ evolution. The total volume of hydrogen produced within 3 h was 103 mL/g. Thus, this study demonstrates that chitosan possesses promising potential in the design of the supported catalysts for cyclohexane oxidation and photocatalytic hydrogen evolution reactions. Full article

In this article, we report on the research on the synthesis of composites based on a porous, highly ordered silica material modified by a metallic nanophase and chitosan biofilm. Due to the ordered pore system of the SBA-15 silica, this material proved to be a good carrier for both the biologically active nanophase (highly dispersed silver nanoparticles, AgNPs) and the adsorption active phase (chitosan). The antimicrobial susceptibility was determined against Gram-positive Staphylococcus aureus ATCC 25923, Gram-negative bacterial strains (Escherichia coli ATCC 25922, Klebsiella pneumoniae ATCC 700603, and Pseudomonas aeruginosa ATCC 27853), and yeast Candida albicans ATCC 90028. The zones of microbial growth inhibition correlated with the content of silver nanoparticles deposited in the composites and were the largest for C. albicans (14–21 mm) and S. aureus (12–17 mm). The suitability of the composites for the purification of water and wastewater from anionic pollutants was evaluated based on kinetic and equilibrium adsorption studies for the dye Acid Red 88. The composite with the highest amount of the chitosan component showed the greatest adsorption capacity (a_m) of 0.57 mmol/g and the most effective kinetics with a rate constant (log k) and half-time (t_0.5) of −0.21 and 1.62 min, respectively. Due to their great practical importance, AgNP–chitosan–silica composites can aspire to be classified as functional materials combining the environmental problem with microbiological activity. Full article

In this work, various types of silica materials were used for the synthesis of chitosan–silica composites. The composites were obtained using the chitosan (Ch) immobilization process from an aqueous solution on various silica phases, i.e., amorphous diatomite (ChAD), crystalline diatomite (ChCD), mesoporous silica MCM-41 (ChMCM), and mesoporous silica SBA-15 (ChSBA). Textural, structural, morphological, and surface properties of the materials were determined by using various measurement techniques, i.e., low-temperature adsorption/desorption isotherms of nitrogen, X-ray diffraction (XRD), small-angle X-ray scattering (SAXS), potentiometric titration, high-resolution transmission electron microscopy (HRTEM), scanning electron microscopy (SEM), and atomic force microscopy (AFM). The adsorption properties towards various anionic dyes, i.e., acid red 88 (AR88), acid orange 8 (AO8), and orange G (OG), were evaluated based on kinetic and equilibrium measurements. The ChSBA, ChAD, and ChMCM composites were characterized by relatively high adsorption capacities (a_m) for AR88, with values equal to 0.78, 0.71, and 0.69 mmol/g, respectively. These composites were also distinguished by the rapid AR88 adsorption rate, with the values of half-time parameter t_0.5 equal to 0.35, 2.84, and 1.53 min, respectively. The adsorption equilibrium and kinetic data were analyzed by applying the generalized Langmuir isotherm and the multi-exponential equation (m-exp), respectively. An interaction mechanism between the dyes and the obtained materials was proposed. Full article

A chitosan–silica hybrid aerogel was synthesized and presented as a potential adsorbent for the purification of cupric ion-contaminated media. The combination of the organic polymer (chitosan), which can be obtained from fishery wastes, with silica produced a mostly macroporous material with an average pore diameter of 33 µm. The obtained aerogel was extremely light (56 kg m⁻³), porous (96% porosity, 17 cm³ g⁻¹ pore volume), and presented a Brunauer–Emmett–Teller surface area (S_BET) of 2.05 m² g⁻¹. The effects of solution pH, aerogel and Cu(II) concentration, contact time, and counterion on cupric removal with the aerogel were studied. Results showed that the initial pH of the cation-containing aqueous solution had very little influence on the removal performance of this aerogel. According to Langmuir isotherm, this material can remove a maximum amount of ca. 40 mg of cupric ions per gram and the kinetic data showed that the surface reaction was the rate-limiting step and equilibrium was quickly reached (in less than one hour). Thus, the approach developed in this study enabled the recovery of waste for the preparation of a novel material, which can be efficiently reused in a new application, namely water remediation. Full article

Peri-implantitis is a growing pathological concern for dental implants which aggravates the occurrence of revision surgeries. This increases the burden on both hospitals and the patients themselves. Research is now focused on the development of materials and accompanying implants designed to resist biofilm formation. To enhance this endeavor, a smart method of biofilm inhibition coupled with limiting toxicity to the host cells is crucial. Therefore, this research aims to establish a proof-of-concept for the pH-triggered release of chlorhexidine (CHX), an antiseptic commonly used in mouth rinses, from a titanium (Ti) substrate to inhibit biofilm formation on its surface. To this end, a macroporous Ti matrix is filled with mesoporous silica (together referred to as Ti/SiO₂), which acts as a diffusion barrier for CHX from the CHX feed side to the release side. To limit release to acidic conditions, the release side of Ti/SiO₂ is coated with crosslinked chitosan (CS), a pH-responsive and antimicrobial natural polymer. Scanning electron microscopy coupled with energy dispersive X-ray spectroscopy (SEM/EDX) and Fourier transform infrared (FTIR) spectroscopy confirmed successful CS film formation and crosslinking on the Ti/SiO₂ disks. The presence of the CS coating reduced CHX release by 33% as compared to non-coated Ti/SiO₂ disks, thus reducing the antiseptic exposure to the environment in normal conditions. Simultaneous differential scanning calorimetry and thermogravimetric analyzer (SDT) results highlighted the thermal stability of the crosslinked CS films. Quartz crystal microbalance with dissipation monitoring (QCM-D) indicated a clear pH response for crosslinked CS coatings in an acidic medium. This pH response also influenced CHX release through a Ti/SiO₂/CS disk where the CHX release was higher than the average trend in the neutral medium. Finally, the antimicrobial study revealed a significant reduction in biofilm formation for the CS-coated samples compared to the control sample using viability quantitative polymerase chain reaction (v-qPCR) measurements, which were also corroborated using SEM imaging. Overall, this study investigates the smart triggered release of pharmaceutical agents aimed at inhibiting biofilm formation, with potential applicability to implant-like structures. Full article

In this work, novel chitosan–silica hydrogels were synthesized and investigated by various complementary techniques. The hydrogels were obtained via the immobilization of chitosan (Ch) on the surface of mesoporous cellular foams (MCFs). The latter silica materials were obtained by a sol–gel process, varying the composition of the reaction mixture (copolymer Pluronic 9400 or Pluronic 10500) and the ageing temperature conditions (80 °C or 100 °C). The role of the silica phase in the hydrogels was the formation of a scaffold for the biopolymeric chitosan component and providing chemical, mechanical, and thermal stability. In turn, the chitosan phase enabled the binding of anionic pollutions from aqueous solutions based on electrostatic interaction mechanisms and hydrogen bonds. To provide information on structural, morphological, and surface properties of the chitosan–silica hydrogels, analyses such as the low-temperature adsorption/desorption of nitrogen, small-angle X-ray scattering (SAXS), scanning electron microscopy (SEM), atomic force microscopy (AFM), and Fourier-transform infrared spectroscopy (FTIR) were performed. Moreover, the verification of the utility of the chitosan–silica hydrogels as adsorbents for water and wastewater treatment was carried out based on kinetic and equilibrium studies of the Acid Red 88 (AR88) adsorption. Adsorption data were analyzed by applying various equations and discussed in terms of the adsorption on heterogeneous solid-surfaces theory. The adsorption mechanism for the AR88 dye–chitosan–silica hydrogel systems was proposed. Full article

The purpose of this study is to identify the steps involved in fabricating silica/chitosan composite membranes and their suitability for fuel cell applications. It also intends to identify the physical characteristics of chitosan composite membranes, including their degree of water absorption, proton conductivity, methanol permeability, and functional groups. In this investigation, composite membranes were fabricated using the solution casting method with a chitosan content of 5 g and silica dosage variations of 2% and 4% while stirring at a constant speed for 2 h. According to the findings, the analysis of composite membranes produced chitosan membranes that were successfully modified with silica. The optimum membrane was found to be 4% s-SiO₂ from the Sol-gel method with the composite membrane’s optimal condition of 0.234 cm/s proton conductivity, water uptake of 56.21%, and reduced methanol permeability of 0.99 × 10⁻⁷ cm²/s in the first 30 min and 3.31 × 10⁻⁷ in the last 150 min. Maintaining lower water uptake capacity at higher silica content is still a challenge that needs to be addressed. In conclusion, the fabricated membranes showed exceptional results in terms of proton conductivity and methanol permeability. Full article

Chitosan and its derivatives are widely used in food packaging, pharmaceutical, biotechnology, medical, textile, paper, agriculture, and environmental industries. However, the flexibility of chitosan films is extremely poor, which limits its relevant applications to a large extent. In this paper, chitosan/sorbitol/nano-silica (CS/sorbitol/SiO₂) composite films were prepared by the casting film method using chitosan, sorbitol, Tween-80 and nano-SiO₂ as raw materials. The structure of the films was characterized by infrared spectroscopy, electron scanning microscopy, and X-ray diffraction analysis. The effects of sorbitol and nano-silica dosage on the mechanical properties, thermal properties and water vapor barrier properties of the composite film were investigated. The results show that with the gradual increase in sorbitol (≤75 wt %), the elongation at the break of chitosan/sorbitol films significantly increased. When the addition of sorbitol was 75 wt %, the elongation at break of the chitosan/sorbitol composite film was 13 times higher than that of the chitosan film. Moreover, nano-SiO₂ can further improve the mechanical properties and thermal stability of the chitosan/sorbitol composite films. When the amount of nano-silica was 4.5 wt %, the composite film became more flexible, with a maximum elongation of 90.8% (which is 14 times that of chitosan film), and its toughness increased to 10.52 MJm⁻³ (which is 6 times that of chitosan film). This study balances the tensile strength and elongation at break of the composite films by adding a plasticizer and nano-filler, providing a reference for the preparation of chitosan composites or their blending with other polymers, and has practical guiding significance for the industrial production of biomass plastics. Full article

A series of new types of composites (biopolymer–silica materials) are proposed as selective and effective adsorbents. A new procedure for the synthesis of chitosan–nanosilica composites (ChNS) and chitosan–silica gel composites (ChSG) using geometrical modification of silica and mechanosorption of chitosan is applied. The highest adsorption efficiency was achieved at pH = 2, hence the desirability of modifications aimed at stabilizing chitosan in such conditions. The amount of chitosan in the synthesis grew to 1.8 times the adsorption capacity for the nanosilica-supported materials and 1.6 times for the silica gel-based composites. The adsorption kinetics of anionic dyes (acid red AR88) was faster for ChNS than for ChSG, which results from a silica-type effect. The various structural, textural, and physicochemical aspects of the chitosan–silica adsorbents were analyzed via small-angle X-ray scattering, scanning electron microscopy, low-temperature gas (nitrogen) adsorption, and potentiometric titration, as well as their adsorption effectiveness towards selected dyes. This indicates the synergistic effect of the presence of dye-binding groups of the chitosan component, and the developed interfacial surface of the silica component in composites. Full article

Recycling of agro-industrial waste is one of the major issues addressed in recent years aimed at obtaining products with high added value as a future alternative to traditional ones in the per-spective of a bio-based and circular economy. One of the most produced wastes is rice husk and it is particularly interesting because it is very rich in silica, a material with a high intrinsic value. In the present study, a method to extract silica from rice husk ash (RHA) and to use it as a carrier for the immobilization of laccase from Trametes versicolor was developed. The obtained mesoporous nano-silica was characterized by X-ray diffraction (XRD), ATR-FTIR spectroscopy, Scanning Elec-tron Microscopy (SEM), and Energy Dispersive X-ray spectroscopy (EDS). A nano-silica purity of about 100% was found. Nano-silica was then introduced in a cross-linked chitosan/alginate scaffold to make it more easily recoverable after reuse. To favor laccase immobilization into the composite scaffold, functionalization of the nano-silica with (γ-aminopropyl) triethoxysilane (APTES) was performed. The APTES/RHA nano-silica/chitosan/alginate (ARCA) composite al-lowed to obtain under mild conditions (pH 7, room temperature, 1.5 h reaction time) a robust and easily reusable solid biocatalyst with 3.8 U/g of immobilized enzyme which maintained 50% of its activity after six reuses. The biocatalytic system, tested for syringic acid bioremediation, was able to totally oxidize the contaminant in 24 h. Full article

Chitosan (CS) is a natural biopolymer that shows promise as a biomaterial for bone-tissue regeneration. However, because of their limited ability to induce cell differentiation and high degradation rate, among other drawbacks associated with its use, the creation of CS-based biomaterials remains a problem in bone tissue engineering research. Here we aimed to reduce these disadvantages while retaining the benefits of potential CS biomaterial by combining it with silica to provide sufficient additional structural support for bone regeneration. In this work, CS-silica xerogel and aerogel hybrids with 8 wt.% CS content, designated SCS8X and SCS8A, respectively, were prepared by sol-gel method, either by direct solvent evaporation at the atmospheric pressure or by supercritical drying in CO₂, respectively. As reported in previous studies, it was confirmed that both types of mesoporous materials exhibited large surface areas (821 m²g⁻¹–858 m²g⁻¹) and outstanding bioactivity, as well as osteoconductive properties. In addition to silica and chitosan, the inclusion of 10 wt.% of tricalcium phosphate (TCP), designated SCS8T10X, was also considered, which stimulates a fast bioactive response of the xerogel surface. The results here obtained also demonstrate that xerogels induced earlier cell differentiation than the aerogels with identical composition. In conclusion, our study shows that the sol-gel synthesis of CS-silica xerogels and aerogels enhances not only their bioactive response, but also osteoconduction and cell differentiation properties. Therefore, these new biomaterials should provide adequate secretion of the osteoid for a fast bone regeneration. Full article