Search Results (342)

Unrefined psyllium husk derived from Plantago ovata constitutes a complex mixture of water-soluble and insoluble polymeric chains that form an interpenetrating network capable of entrapping carbon nanoparticles. While the resulting composite was found to swell in aqueous electrolyte, it exhibited hydrogel-like properties where the electrochemical activity was retained and found to be stable upon repetitive voltammetric cycling. Planar film systems were characterized by electron microscopy, Raman spectroscopy, tensile testing, gravimetric analysis, contact angle and cyclic voltammetry. A key advantage of the composite lies in its ability to be cast in 3D geometric forms such as pyramidal microneedle arrays (700 μm high × 200 μm base × 500 μm pitch) that could serve as viable electrode sensors. In contrast to conventional composite electrode materials that rely on non-aqueous solvents, the psyllium mixture is processed entirely from an aqueous solution. This, along with its plant-based origins and simple processing requirements, provides a versatile matrix for the design of biodegradable electrode structures that can be manufactured from more sustainable sources. Full article

Prolonged drought and soil degradation severely affect soil fertility and limit crop productivity. Superabsorbent hydrogels offer an effective solution for improving water retention in soil and supporting plant growth. In this work, we examined the performance of superabsorbent hydrogels based on sodium alginate, acrylic acid (AA), and poly (ethylene oxide) (PEO) cross-linked with 12.5 kGy using e-beam irradiation. The hydrogels were assessed in various aqueous environments by examining network characteristics, swelling capacity, and swelling kinetics to evaluate the impact of water’s electrical conductivity (which ranges from 0.05 to 321 μS/cm). Morphological and chemical structure changes were evaluated using SEM and FTIR techniques. The results demonstrated that water conductivity significantly affected the physicochemical properties of the hydrogels. Swelling behavior showed notable sensitivity to electrical conductivity variations, with swelling degrees reaching 28,400% at 5 μS/cm and 14,000% at 321 μS/cm, following first-order and second-order kinetics. FTIR analysis confirmed that structural modifications correlated with water conductivity, particularly affecting the O–H, C–H, and COOH groups sensitive to the ionic environment. SEM characterization revealed a porous morphology with an interconnected microporous network that facilitates efficient water diffusion. These hydrogels show exceptional swelling capacity and are promising candidates for sustainable agriculture applications. Full article

A metal-ion-free method was developed to prepare κ-carrageenan/cellulose hydrogel beads for efficient cationic dye removal. The beads were fabricated using a mixture of 1-ethyl-3-methylimidazolium acetate and N,N-dimethylformamide as the solvent system, followed by aqueous ethanol-induced phase separation. This process eliminated the need for metal-ion crosslinkers, which typically neutralize anionic sulfate groups in κ-carrageenan, thereby preserving a high density of accessible binding sites. The resulting beads formed robust interpenetrating polymer networks. The initial swelling ratio reached up to 28.3 g/g, and even after drying, the adsorption capacity remained over 50% of the original. The maximum adsorption capacity for crystal violet was 241 mg/g, increasing proportionally with κ-carrageenan content due to the higher surface concentration of anionic sulfate groups. Kinetic and isotherm analyses revealed pseudo-second-order and Langmuir-type monolayer adsorption, respectively, while thermodynamic parameters indicated that the process was spontaneous and exothermic. The beads retained structural integrity and adsorption performance across pH 3–9 and maintained over 90% of their capacity after five reuse cycles. These findings demonstrate that κ-carrageenan/cellulose hydrogel beads prepared via a metal-ion-free strategy offer a sustainable and effective platform for cationic dye removal from wastewater, with potential for heavy metal ion adsorption. Full article

Myocardial infarction (MI) remains one of the most common cardiovascular diseases and a leading cause of morbidity and mortality worldwide. In recent years, natural polymeric patches have attracted increasing attention as a promising therapeutic platform for myocardial tissue repair. This study explored the fabrication and evaluation of screen-printed electrodes (SPEs) on chitosan film as a novel platform for cardiac patch applications. Chitosan is a biodegradable and biocompatible natural polymer that provides an ideal substrate for SPEs, providing mechanical stability and promoting cell adhesion. Silver ink was employed to enhance electrochemical performance, and the electrodes exhibited strong adhesion and structural integrity under wet conditions. Mechanical testing and swelling ratio analysis were conducted to assess the patch’s physical robustness and aqueous stability. Silver ink was employed to enhance electrochemical performance, which was evaluated using cyclic voltammetry. In vitro, electrical stimulation through the chitosan–SPE patch significantly increased the expression of cardiac-specific genes (GATA-4, β-MHC, troponin I) in bone marrow mesenchymal stem cells (BMSCs), indicating early cardiogenic differentiation potential. In vivo, the implantation of the chitosan–SPE patch in a rat MI model demonstrated good tissue integration, preserved myocardial structure, and enhanced ventricular wall thickness, indicating that the patch has the potential to serve as a functional cardiac scaffold. These findings support the feasibility of screen-printed electrodes fabricated on chitosan film substrates as a cost-effective and scalable platform for cardiac repair, offering a foundation for future applications in cardiac tissue engineering. Full article

Cellulose nanofiber (CNF) treatments can enhance the structure and performance of regenerated cellulose fibers. This study investigates the effects of CNF treatment on the mechanical properties, water absorption behavior, and humidity dependence of regenerated cellulose fibers. Tensile testing demonstrated that CNF-treated fibers exhibit improved elasticity and reduced swelling in aqueous environments. Scanning electron microscopy revealed the adsorption of CNF components onto the fiber surfaces. Microbeam X-ray diffraction indicated structural differences between untreated and CNF-treated fibers, with the latter containing cellulose I crystals. Small-angle X-ray scattering revealed alterations in the internal fibrillar structure due to CNF treatment. FT-IR spectroscopy highlighted humidity-dependent variations in molecular vibrations, with peak intensities increasing under higher humidity conditions. Additionally, CNF treatment inhibited water absorption in high-humidity conditions, contributing to reduced expansion rates and increased elastic modulus during water absorption. Overall, CNF treatment enhanced both the mechanical strength and water resistance of regenerated cellulose fibers, making them suitable for advanced textile applications. This study provides valuable insights into the role of CNF-treated fibers in improving the durability and functional performance of regenerated cellulose-based textile. Full article

Poly(acrylic acid) (PAA) and hydroxypropylcellulose (HPC) hydrogels were synthesized in the absence of a crosslinker. Chemical crosslinking between PAA and HPC was demonstrated through free radical polymerization by a precipitation reaction in acetone as the solvent. These hydrogels exhibited smaller swelling ratios (1 to 5 g H₂O/g) than homo PAA hydrogels synthesized in water as the solvent. They were swollen in a 0.1 M NaOH solution and subsequently used to remove Ni²⁺ ions from aqueous solutions with concentrations ranging from 1000 to 4000 ppm. The absorption capacity of these hydrogels ranged from 91 to 340 mg of Ni²⁺/g in a rapid 1 h process, and from 122 to 435 mg of Ni²⁺/g in a 24 h process, demonstrating an improvement in Ni²⁺ absorption compared to previously reported hydrogels. The colored 1000 and 2000 ppm Ni²⁺ solutions became clear after treatment, while the PAA-HPC hydrogels turned green due to the uptake of Ni²⁺ ions, which were partially chelated by carboxylate groups as nickel polyacrylate and partially precipitated as Ni(OH)₂, resulting in an average absorption efficiency of 80%. The hydrogel was able to release the absorbed Ni²⁺ upon immersion in an HCl solution, with an average release percentage of 76.4%, indicating its potential for reuse. These findings support the use of PAA-HPC hydrogels for cleaning Ni²⁺-polluted water. The cost of producing 1 g of these hydrogels in laboratory conditions is approximately 0.2 USD. Full article

The advancement of non-aqueous redox flow batteries (NARFBs) remains significantly constrained by the absence of membranes with sufficient ionic selectivity and chemical compatibility. Herein, we fabricated flexible membranes incorporating metal–organic framework (MOF) via a solution casting approach. The rigid framework structure of the MOF effectively suppresses membrane swelling in organic solvents. The appropriate structural pore of MOF enables a size-sieving effect toward redox-active materials and supporting electrolyte, thereby reducing material crossover and enhancing the ionic selectivity of the composite membranes. The batteries with the designed composite membranes exhibit a Coulombic efficiency of higher than 99% and significantly improved cycling stability at 10 mA cm⁻². The membrane design strategy, employing MOF materials with a structural pore size between the molecular size of the supporting electrolyte and active materials, is universal for NARFB. Full article

The effects of 1-N-naphthylphthalamic acid (NPA) applied as an aqueous solution on uncooled grape hyacinth (Muscari armeniacum) bulbs were investigated, focusing on histological measurements and the determination of various metabolites in developing roots. M. armeniacum bulbs were kept for a defined number of days in distilled water (control) or aqueous NPA solutions, and then 2 cm sections of root tips were taken for histological measurements. Longitudinal and cross sections were taken in these root pieces, followed by measurements of their basic parts and microscopic images. Determinations of polar compounds by GC/MS and phenolic metabolites by HPLC/MS/MS were carried out in freeze-dried root samples. NPA inhibited the growth of the roots and caused swelling of their elongation parts, as well as changes in the dimensions of other parts of the roots and disruption of the gravitropic direction of their growth. However, NPA did not affect leaf growth and the amino acid, organic acid, and major carbohydrate content in the roots, but increased the level of unknown saccharides, probably oligofructans. The decrease in the contents of many phenolic compounds observed in our study under the influence of NPA may indicate that this could be one of the symptoms/causes of root growth disorders. In turn, the reduction in polyphenol levels may have been related to an increase in the number and length of root hairs. Full article

The mechanical properties of cell scaffolds are strongly influenced by their hydration state. In this study, we investigated the effect of the aqueous phase on the elastic modulus of chitosan hydrogel films using two complementary techniques: uniaxial tensile testing and atomic force microscopy (AFM) nanoindentation. Our results demonstrate that hydration markedly reduced the elastic modulus, decreasing from approximately 2 GPa in dry films to 120 kPa in swollen films, primarily due to the plasticizing effect of water. Moreover, hydrogel films in equilibrium with the aqueous phase exhibited a Young’s modulus three times lower than that of swollen films not in equilibrium. Raman spectroscopy further reveals a solvent “squeeze-out” phenomenon, as evidenced by an increased signal intensity in the 850–1200 cm⁻¹ region for stretched films that were out of swelling equilibrium, whereas equilibrated films showed stable spectral features. These findings highlight the crucial role of hydration dynamics in determining the mechanical behavior of chitosan hydrogel films, offering valuable insights for tailoring their properties in biomedical scaffold applications. Full article

Electroless nickel deposition (ELD) on polymer substrates enables the fabrication of flexible, conductive fibres for wearable and functional textiles. However, achieving uniform, low-defect coatings on synthetic fibres such as nylon-6,6 remains challenging due to their chemical inertness, hydrophobicity, and poor interfacial compatibility with metal coatings. This study presents a solvent-assisted approach using dimethyl sulfoxide (DMSO) in a conventional aqueous ELD bath to control both polymer–metal interfacial chemistry and nickel coating microstructure. The modified surface supports dense catalytic sites, triggering spatially uniform Ni nucleation. The combination of scanning electron microscopy and transmission electron microscopy confirms the difference in coarse grains with fully aqueous baths to a nanocrystalline shell with DMSO-modified baths. This refined microstructure relieves residual stress and anchors firmly to the swollen polymer, delivering +7 °C higher onset decomposition temperature and 45% lower creep strain at 50 °C compared with aqueous controls. The fabric strain sensor fabricated by 1 wt.% DMSO-modified ELD shows a remarkable sensitivity against strain, demonstrating a 1400% resistance change under 200% stain. Electrochemical impedance and polarisation tests confirm a two-fold rise in charge transfer resistance and negligible corrosion current drift after accelerated ageing. By clarifying how a polar aprotic co-solvent couples polymer swelling with metal growth kinetics, the study introduces a scalable strategy for tuning polymer–metal interfaces and advances solvent-assisted ELD as a route to mechanically robust, thermally stable, and corrosion-resistant conductive textiles. Full article

The starch modification of mango cotyledons with both single ultrasound (US) and dual (US followed by octenyl succinic anhydride, OSA) was optimized by response surface methodology (RSM). The mechanochemical effects of ultrasound on amylose content, particle size, and dual modification efficiency were assessed. In addition, the structural, thermal, morphological, and functional properties were evaluated. After optimization with single US (41 min and 91% sonication intensity), sonication induced starch granule fragmentation, altering amorphous and partially crystalline regions, which increased amylose content (34%), reduced particle size (Dx50 = 12 μm), and modified granule surface morphology. The dual modification (the subsequent OSA reaction lasted 4.6 h under the same conditions) reached a degree of substitution of 0.02 and 81% efficiency, imparting amphiphilic properties to the starch. OSA groups were mainly incorporated into amorphous and surface regions, which decreased crystallinity, gelatinization temperature, and enthalpy. The synergistic effect of the modification with US and OSA in the dual modification significantly improved the solubility and swelling power of starch, resulting in better dispersion, functionality in aqueous systems, and chemical reactivity. These findings highlight the potential of dual modification to transform mango cotyledon starch into a versatile ingredient in the food industry as a thickener, a stabilizer in soups and sauces, an emulsifier, a carrier of bioactive and edible films; in the cosmetic industry as a gelling and absorbent agent; and in the pharmaceutical industry for the controlled release of drugs. Furthermore, valorizing mango cotyledons supports circular economy principles, promoting sustainable and value-added food product development. Full article

Background/Objectives: The rise of bacterial resistance and the search for alternative, biocompatible antimicrobial materials have driven interest in natural-based nanocomposites. In this context, silver nanoparticles (AgNPs) have shown broad-spectrum antibacterial activity, and bacterial cellulose (BC) is widely recognized for its high purity, hydrophilicity, and biocompatibility. This study aimed to develop a bio-based BC–AgNP nanocomposite via green synthesis using Astrocaryum aculeatum (tucumã) extract and assess its antimicrobial performance for wound dressing applications. Methods: BC was biosynthesized via green tea fermentation (20 g/L tea and 100 g/L sugar) and purified prior to use. AgNPs were obtained by reacting aqueous tucumã extract with silver nitrate (0.1 mmol/L) at pH (9) and temperature (40 °C). BC membranes were immersed in the AgNPs dispersion for 7 days to form the nanocomposite. Characterization was performed using UV–Vis, DLS, TEM, SEM–EDS, FTIR, XRD, ICP–OES, and swelling analysis. Antibacterial activity was evaluated using the disk diffusion method against Staphylococcus aureus and Escherichia coli (ATCC 6538 and 4388). Results: The UV–Vis spectra revealed a gradual decrease in the surface plasmon resonance (SPR) band over 7 days of incubation with BC, indicating progressive incorporation of AgNPs into the membrane. ICP analysis confirmed silver incorporation in the BC membrane at 0.00215 mg/mL, corresponding to 15.5% of the initial silver content. Antimicrobial assays showed inhibition zones of 6.5 ± 0.5 mm for S. aureus and 4.3 ± 0.3 mm for E. coli. Conclusions: These findings validate the successful formation and antimicrobial performance of the BC–AgNP nanocomposite, supporting its potential use in wound care applications. Full article

The optical ammonia-sensing properties of water-dispersible polyaniline (PANI) complexes chemically synthesized in the presence of polysulfonic acids of different structure and chain flexibility were compared for the first time. Flexible-chain poly(styrene-4-sulfonic acid) and poly-(2-acrylamido-2-methyl-1-propanesulfonic acid), as well as semi-rigid-chain poly-4,4′-(2,2′-disulfonic acid)diphenylene-iso-phthalamide and rigid-chain poly-4,4′-(2,2′-disulfonic acid)diphenylene-tere-phthalamide (t-PASA) were used. The sensor films were prepared by a convenient and scalable method—spray coating of aqueous solutions on glass substrates. The optical response time and amplitude of the sensor films in the range of ammonia concentrations from 5 to 200 ppm were investigated. To overcome the influence of humidity and presence of over-stoichiometric protons of the polyacid on the accuracy of ammonia determination treatments of the films in aqueous solutions of NaCl, CaCl₂ and BaCl₂ were tested. The treatment in 1 M CaCl₂ solution for all of the PANI complexes results in a significant improvement in the response time, amplitude and reproducibility. The films of PANI complexes with the flexible-chain polyacids have the highest response amplitude in the range of ammonia concentrations 5–25 ppm. PANI-t-PASA film demonstrated the best sensory properties at ammonia concentrations more than 50 ppm. FTIR spectroscopy showed that CaCl₂ treatment results in cross-linking of sulfoacid groups from adjacent polyacid chains by Ca²⁺ ions. Thus, such a treatment results both in the neutralization of excessive protons and a significant reduction in the films’ swelling at high humidity. Full article

This paper reports several preliminary investigations concerning the relative humidity (RH) detection response of a chemiresistive sensor that uses a novel sensing layer based on pristine carbon nano-onions (CNOs) and polyvinyl alcohol (PVA) at a 1/1 and 2/1 w/w ratio. The sensing device, including a Si/SiO₂ substrate and gold electrodes, is obtained by depositing the CNOs–PVA aqueous suspension on the sensing structure by drop casting. The composition and morphology of the sensing film are explored by means of scanning electron microscopy, Raman spectroscopy, atomic force microscopy, and X-ray diffraction. The manufactured sensor’s room temperature RH detection performance is examined by applying a continuous flow of the electric current between the interdigitated electrodes and measuring the voltage as the RH varies from 5% to 95%. For RH below 82% (sensing layer based on CNOs–PVA at 1/1 w/w ratio) or below 50.5% (sensing layer based on CNOs–PVA at 2/1 w/w ratio), the resistance varies linearly with RH, with a moderate slope. The newly developed sensor, using CNOs–PVA at a 1:1 ratio (w/w), responded as well as or better than the reference sensor. At the same time, the recorded recovery time was about 30 s, which is half the recovery time of the reference sensor. Additionally, the changes in resistance (ΔR/ΔRH) for different humidity levels showed that the CNOs–PVA layer at 1:1 was more sensitive at humidity levels above 80%. The main RH sensing mechanisms considered and discussed are the decrease in the hole concentration in the CNOs during the interaction with an electron donor molecule, such as water, and the swelling of the hydrophilic PVA. The experimental RH detection data are analyzed and compared with the RH sensing results reported in previously published work on RH detectors employing sensing layers based on oxidized carbon nanohorns–polyvinylpirrolidone (PVP), oxidized carbon nanohorns–PVA and CNOs–polyvinylpyrrolidone. Full article

Sustainable ethylene propylene diene monomer (EPDM) elastomers are gaining traction as eco-friendly sealing materials in fuel cell applications. This study evaluates the mechanical degradation behavior of two ECO EPDM formulations—one reinforced with circular carbon black (CCB EPDM), and the other with recycled carbon black (RCB EPDM)—under conditions representative of acidic fuel cell environments. The samples underwent thermal aging at 90 °C for 1000 h, and were immersed in aqueous H₂SO₄ solutions of varying concentrations (1 M, 0.1 M, and 0.001 M) for 1000 h at the same temperature. Gravimetric and volumetric swelling measurements revealed that RCB EPDM experienced significantly higher mass and volume uptake, particularly at intermediate acid concentration, indicating greater susceptibility to fluid ingress. Mechanical testing, including measurement of tensile strength, Shore A hardness, and IRHD microhardness, showed that while RCB EPDM exhibited higher initial strength, it degraded more severely under thermal and acidic exposure. SEM-EDS analysis revealed microstructural damage and compositional changes, with RCB EPDM displaying more pronounced oxidation and surface erosion. In contrast, CCB EPDM demonstrated greater retention of mechanical integrity, greater dimensional stability, and lower variability across aging conditions. These findings highlight the advantages of circular carbon black in enhancing the durability of ECO EPDM compounds in acidic and thermally dynamic fuel cell environments. Full article