Search Results (17)

Cellulose is a versatile biopolymer increasingly applied in medicine and industry due to its biodegradability and biocompatibility, along with the renewability and large availability of source materials. However, finding simple, eco-friendly, and effective methods to modify cellulose to provide it with new functionalities remains a challenge. This work presents a new, inexpensive, and eco-friendly method to chemically modify microcrystalline cellulose (MCC) by the submerged cold plasma treatment of an aqueous suspension of MCC containing different oxidizing agents, such as hydrogen peroxide (H₂O₂), sodium hypochlorite (NaClO), or sodium periodate (NaIO₄). Fourier-transform Infrared (FTIR) and X-ray photoelectron spectroscopy (XPS) showed that plasma treatment intensified the oxidizing effect of H₂O₂, NaClO, and NaIO₄, with plasma-assisted NaClO treatment yielding the highest MCC oxidation level. XPS indicated that the plasma-assisted oxidations also resulted in different degrees of chemical degradation of MCC, a finding further supported by the thermogravimetric analysis (TGA) results. X-ray diffraction (XRD) data revealed a different effect of the oxidizing agents on the crystalline and amorphous regions in MCC. Scanning electron microscopy (SEM) images showed that the combined treatment with plasma and chemical oxidizing agents led to MCC fragmentation and varying degrees of defibrillation into nanofibers. Full article

Piezoelectric sensors convert mechanical stress into electrical charge via the piezoelectric effect, and when fabricated as fibers, they offer flexibility, lightweight properties, and adaptability to complex shapes for self-powered wearable sensors. Polyvinylidene fluoride (PVDF) nanofibers have garnered significant interest due to their potential applications in various fields, including sensors, actuators, and energy-harvesting devices. Achieving optimal piezoelectric properties in PVDF nanofibers requires the careful optimization of polarization. Applying a high electric field to PVDF chains can cause significant mechanical deformation due to electrostriction, leading to crack formation and fragmentation, particularly at the chain ends. Therefore, it is essential to explore methods for polarizing PVDF at the lowest possible voltage to prevent structural damage. In this study, a Design of Experiments (DoE) approach was employed to systematically optimize the polarization parameters using a definitive screening design. The main effects of the input parameters on piezoelectric properties were identified. Heat treatment and the electric field were significant factors affecting the sensor’s sensitivity and β-phase fraction. At the highest temperature of 120 °C and the maximum applied electric field of 3.5 kV/cm, the % β-phase (F(β)) exceeded 95%. However, when reducing the electric field to 1.5 kV/cm and 120 °C, the % F(β) ranged between 87.5% and 90%. The dielectric constant (ɛ′) of polarized PVDF was determined to be 30 at an electric field frequency of 1 Hz, compared to a value of 25 for non-polarized PVDF. The piezoelectric voltage coefficient (g₃₃) for polarized PVDF was measured at 32 mV·m/N at 1 Hz, whereas non-polarized PVDF exhibited a value of 3.4 mV·m/N. The findings indicate that, in addition to a high density of β-phase dipoles, the polarization of these dipoles significantly enhances the sensitivity of the PVDF nanofiber mat. Full article

This study evaluated the mechanical performance of a cellulose nanocrystal (CNC)-based composite, consisting of hydroxyapatite and natural fibers, mimicking the mechanical properties of real bone. The effect of natural nanofibers on the cutting force of the composite was evaluated for suitability in surgical training. Although hydroxyapatite has been extensively studied in bone-related applications, the exploration of epoxy-based composites incorporating both hydroxyapatite and CNC represents a novel approach. The evaluation involved a load cell with an oscillating saw. The uniform distribution of CNCs within the composite was assessed using 3D X-ray imaging. The cutting force was found to be 4.005 ± 0.5469 N at a feed rate of 0.5 mm/s, comparable to that required when cutting real bone with the osteon at 90°. The 90-degree orientation of the osteon aligns with the cutting direction of the oscillating saw when performing knee replacements on the tibia and femur bones. The addition of CNCs resulted in changes in fracture toughness, leading to increased material fragmentation and surface irregularities. Furthermore, the change in the cutting force with depth was similar to that of real bone. The developed composite material enables bone-cutting surgeries using bioceramics and natural fibers without the risks associated with cadavers or synthetic fibers. Mold-based computed tomography data allows for the creation of various bone forms, enhancing skill development for surgeons. Full article

Myocardial remodeling is an inevitable risk factor for cardiac arrhythmias and can potentially be corrected with cell therapy. Although the generation of cardiac cells ex vivo is possible, specific approaches to cell replacement therapy remain unclear. On the one hand, adhesive myocyte cells must be viable and conjugated with the electromechanical syncytium of the recipient tissue, which is unattainable without an external scaffold substrate. On the other hand, the outer scaffold may hinder cell delivery, for example, making intramyocardial injection difficult. To resolve this contradiction, we developed molecular vehicles that combine a wrapped (rather than outer) polymer scaffold that is enveloped by the cell and provides excitability restoration (lost when cells were harvested) before engraftment. It also provides a coating with human fibronectin, which initiates the process of graft adhesion into the recipient tissue and can carry fluorescent markers for the external control of the non-invasive cell position. In this work, we used a type of scaffold that allowed us to use the advantages of a scaffold-free cell suspension for cell delivery. Fragmented nanofibers (0.85 µm ± 0.18 µm in diameter) with fluorescent labels were used, with solitary cells seeded on them. Cell implantation experiments were performed in vivo. The proposed molecular vehicles made it possible to establish rapid (30 min) electromechanical contact between excitable grafts and the recipient heart. Excitable grafts were visualized with optical mapping on a rat heart with Langendorff perfusion at a 0.72 ± 0.32 Hz heart rate. Thus, the pre-restored grafts’ excitability (with the help of a wrapped polymer scaffold) allowed rapid electromechanical coupling with the recipient tissue. This information could provide a basis for the reduction of engraftment arrhythmias in the first days after cell therapy. Full article

The de novo design and synthesis of peptide-based biocatalysts that can mimic the activity of natural enzymes is an exciting field with unique opportunities and challenges. In a natural enzyme, the active site is composed of an assembly of different amino acid residues, often coordinated with a metal ion. A metalloenzyme’s catalytic activity results from the dynamic and concerted interplay of various interactions among the residues and metal ions. Aiming to mimic such enzymes, simple peptide fragments, drawing structural inspiration from natural enzymes, can be utilized as a model. In our effort to mimic a metal-containing hydrolase, we designed peptide amphiphiles (PA) 1 and 2 with a terminal histidine having amide and acid functionalities, respectively, at its C-terminal, imparting differential ability to coordinate with Zn and Cu ions. The PAs demonstrate remarkable self-assembly behavior forming excellent nanofibers. Upon coordination with metal ions, depending on the coordination site the nanofibers become rigidified or weakened. Rheological studies revealed excellent mechanical properties of the hydrogels formed by the PAs and the PA–metal co-assemblies. Using such co-assemblies, we mimic hydrolase activity against a p-nitrophenyl acetate (p-NPA) substrate. Michaelis–Menten’s enzyme kinetic parameters indicated superior catalytic activity of 2 with Zn amongst all the assemblies. Full article

The development of new heterogeneous Pt-containing catalysts has retained its relevance over the past decades. The present paper describes the method to produce metal–carbon composites, Pt_1−xNi_x/CNF, with an adjustable Pt/Ni ratio. The composites represent Pt_1−xNi_x (x = 0.0–1.0) nanoparticles embedded within a structure of carbon nanofibers (CNF). The synthesis of the composites is based on a spontaneous disintegration of Pt_1−xNi_x alloys in an ethylene-containing atmosphere with the formation of CNF. The initial Pt_1−xNi_x alloys were prepared by thermolysis of multicomponent precursors. They possess a porous structure formed by fragments of 100–200 nm. As was shown by X-ray diffraction analysis, the crystal structure of the alloys containing 0–30 and 60–100 at.% Ni corresponds to a fcc lattice based on platinum (Fm-3m), while the Pt_0.50Ni_0.50 sample is an intermetallic compound with the tetragonal structure (P4/mmm). The impact of the Ni content in the Pt_1−xNi_x samples on their activity in ethylene decomposition was studied as well. As was revealed, the efficiency of Pt_1−xNi_x alloys in this process increases with the rise of Ni concentration. The composite samples were examined in an electrochemical hydrogen evolution reaction. The synthesized Pt_1-xNi_x/CNF composites demonstrated superior activity if compared with the Pt/Vulcan commercial catalyst. Full article

The synthesis and characterization of fibrous materials with a hierarchical structure are of great importance for materials sciences. Among this class of materials, microfibers of different natures coated with carbon nanofibers attract special interest. Such coating modifies the surface of microfibers, makes it rougher, and thus strengthens its interaction with matrices being reinforced by the addition of these microfibers. In the present work, a series of hierarchical materials based on carbon microfibers, basalt microfibers, and fiberglass cloth coated with up to 50 wt% of carbon nanofibers was synthesized via the catalytic chemical vapor deposition technique. The initial items were impregnated with an aqueous solution of nickel nitrate and reduced in a hydrogen flow. Then, the catalytic chemical vapor deposition process using C₂H₄ or C₂H₄Cl₂ as a carbon source was carried out. A simple and cost-effective technique for the preparation of the samples of hierarchical materials for transmission electron microscopy examination was developed and applied for the first time. The proposed method of sample preparation for sequential TEM visualization implies an ultrasonic treatment of up to four samples simultaneously under the same conditions by using a special sample holder. As was found, the relative strength of carbon nanofibers coating the surface of microfibers decreases in the order of CNF/CMF > CNF/BMF > CNF/FGC. Two effects of the ultrasonic action on the carbon coating were revealed. First, strongly bonded carbon nanofibers undergo significant breakage. Such behavior is typical for carbon and basalt microfibers. Secondly, carbon nanofibers can be completely detached from the microfiber surface, as was observed in the case of fiberglass cloth. In the case of CNF/CMF material, the graphitized surface of carbon microfiber is coherent with the structure of carbon nanofiber fragments grown on it, which explains the highest adhesion strength of the carbon nanolayer coated on carbon microfibers. Full article

A network of nanofibers is formed in situ through solid-state deformation of disentangled ultra-high molecular weight polyethylene (dis-UHMWPE) during compounding with a polyolefin elastomer below the melting temperature of dis-UHMWPE crystals. Dis-UHMWPE was prepared in the form of powder particles larger than 50 μm by polymerization at low temperatures, which favored the crystallization and prevention of macromolecules from entangling. Shearing the blend for different durations and at different temperatures affects the extent to which the grains of dis-UHMWPE powder deform into nanofibers. Disentangled powder particles could deform into a network of nanofibers with diameters between 110 and 340 nm. The nanocomposite can be further sheared for a longer time to decrease the diameter of dis-UHMWPE nanofibers below 40 nm, being still composed of ≈70 wt.% of crystalline and ≈30 wt.% of amorphous components. Subsequently, these thinner fibers begin to melt and fragment because they are thinner and also because the amorphous defects locally decrease the nanofibers’ melting temperature, which results in their fragmentation and partial loss of nanofibers. These phenomena limit the thickness of dis-UHMWPE nanofibers, and this explains why prolonged or more intense shearing does not lead to thinner nanofibers of dis-UHMWPE when compounded in a polymeric matrix. Full article

A flexible N-doped carbon nanofiber membrane loaded with Nb and Ni nanoparticles (Nb/Ni@NC) was prepared using electrospinning technology and a subsequent thermal annealing method and used as a self-supporting anode material for lithium-ion batteries. The Nb/Ni@NC nanofiber membrane had excellent flexibility and could be folded and bent at will without fragmentation and wrinkling; the nanofibers also had a uniform and controllable morphology with a diameter of 300–400 nm. The electrochemical results showed that the flexible Nb/Ni@NC electrode could deliver a high discharge capacity of 378.7 mAh g⁻¹ after 200 cycles at 0.2 A g⁻¹ and an initial coulombic efficiency of 67.7%, which was higher than that of the pure flexible NC anode in contrast. Moreover, a reversible discharge capacity of 203.6 mAh g⁻¹ after 480 cycles at 1.0 A g⁻¹ was achieved by the flexible Nb/Ni@NC electrode with a capacity decay for each cycle of only 0.075%, which showed an excellent rate capability and cycling stability. Full article

Currently, the fast growth and advancement in technologies demands promising supercapacitors, which urgently require a distinctive electrode material with unique structures and excellent electrochemical properties. Herein, binder-free manganese iron sulfide (Mn–Fe–S) nanostructures were deposited directly onto Ni-foam through a facile one-step electrodeposition route in potentiodynamic mode. The deposition cycles were varied to investigate the effect of surface morphologies on Mn–Fe–S. The optimized deposition cycles result in a fragmented porous nanofibrous structure, which was confirmed using Field Emission Scanning Electron Microscopy (FE−SEM). X-ray photoelectron spectroscopy (XPS) confirmed the presence of Mn, Fe, and S elements. The energy dispersive X-ray spectroscopy and elemental mapping revealed a good distribution of Mn, Fe, and S elements across the Ni-foam. The electrochemical performance confirms a high areal capacitance of 795.7 mF cm⁻² with a 24 μWh cm⁻² energy density calculated at a 2 mA cm⁻² current density for porous fragmented nanofiber Mn–Fe–S electrodes. The enhancement in capacitance is due to diffusive-controlled behavior dominating the capacitator, as shown by the charge–storage kinetics. Moreover, the assembled asymmetric coin cell device exhibited superior electrochemical performance with an acceptable cyclic performance of 78.7% for up to 95,000 consecutive cycles. Full article

The main aim of this study is to investigate the effect of fragmentation of electrospun carbon nanofibers (eCNFs) obtained at different temperatures, i.e., at 750 °C, 1000 °C, 1500 °C, 1750 °C and 2000 °C on the cellular response in vitro. In order to assess the influence of nanofibers on biological response, it was necessary to conduct physicochemical, microstructural and structural studies such as SEM, XPS, Raman spectroscopy, HRTEM and surface wettability of the obtained materials. During the in vitro study, all samples made contact with the human chondrocyte CHON-001 cell lines. The key study was to assess the genotoxicity of eCNFs using the comet test after 1 h or 24 h. Special attention was paid to the degree of crystallinity of the nanofibers, the dimensions of the degradation products and the presence of functional groups on their surface. A detailed analysis showed that the key determinant of the genotoxic effect is the surface chemistry. The presence of nitrogen-containing groups as a product of the decomposition of nitrile groups has an influence on the biological response, leading to mutations in the DNA. This effect was observed only for samples carbonized at lower temperatures, i.e., 750 °C and 1000 °C. These results are important with respect to selecting the temperature of thermal treatment of eCNFs dedicated for medical and environmental functions due to the minimization of the genotoxic effect of these materials. Full article

The research is focused on the dynamic compressive strength, impact toughness and the distribution law of fragmentation size for the plain concrete and the carbon nanofiber reinforced concrete with four fiber volume contents (0.1%, 0.2%, 0.3% and 0.5%) under impact load by using the Φ100 mm split-Hopkinson pressure bar. Based on the fractal theory and considering the micropore structure characteristics of the specimen, the impact of the strain rate and the dosage of carbon nanofibers on the dynamic mechanical performance of concrete is analyzed. According to the results, both the dynamic compressive strength and the impact toughness increase continuously with the improvement of the strain rate level at the same dosage of fiber, showing strong strain rate strengthening effect; at the same strain rate level, the impact toughness increases gradually with the increase in the fiber dosage, while the dynamic compressive strength tends to increase at first and then decrease; the distribution of the fragmentation size of concrete is a fractal in statistical sense, in general, the higher the strain rate level, the higher the number of fragments, the lower the size, and the larger the fractal dimension; the optimal dosage of carbon nanofibers to improve the dynamic compressive strength of concrete is 0.3%, and the pore structure characteristics of carbon nanofiber reinforced concrete exhibit obvious fractal features. Full article

Coal-derived carbon nanofibers (CCNFs) have been recently found to be a promising and low-cost electrode material for high-performance supercapacitors. However, the knowledge gap still exists between holistic understanding of coal precursors derived from different solvents and resulting CCNFs’ properties, prohibiting further optimization of their electrochemical performance. In this paper, assisted by laser desorption/ionization (LDI) and gas chromatography–mass spectrometry (GC–MS) technologies, a systematic study was performed to holistically characterize mass distribution and chemical composition of coal precursors derived from various ionic liquids (ILs) as extractants. Sequentially, X-ray photoelectron spectroscopy (XPS) revealed that the differences in chemical properties of various coal products significantly affected the surface oxygen concentrations and certain species distributions on the CCNFs, which, in turn, determined the electrochemical performances of CCNFs as electrode materials. We report that the CCNF that was produced by an oxygen-rich coal fragment from C₆mimCl ionic liquid extraction showed the highest concentrations of quinone and ester groups on the surface. Consequentially, C₆mimCl-CCNF achieved the highest specific capacitance and lowest ion diffusion resistance. Finally, a symmetric carbon/carbon supercapacitor fabricated with such CCNF as electrode delivered an energy density of 21.1 Wh/kg at the power density of 0.6 kW/kg, which is comparable to commercial active carbon supercapacitors. Full article

Polymer–polymer systems with special phase morphology were prepared, leading to an exceptional combination of strength, modulus, and ductility. Two immiscible polymers: poly(ε-caprolactone) (PCL) and polyhydroxyalkanoate (PHA) were used as components for manufacturing a nanoblend and a nanocomposite characterized by nanodroplet-matrix and nanofibril-matrix morphologies, respectively. Nanofibrils were formed by high shear of nanodroplets at sufficiently low temperature to stabilize their fibrillar shape by shear-induced crystallization. The effects of nanodroplet vs. nanofiber morphology on the tensile mechanical behavior of the nanocomposites were elucidated with the help of in situ 2D small-angle X-ray scattering, microcalorimetry and 2D wide-angle X-ray diffraction. For neat PCL and a PCL/PHA blend, the evolution of the structure under uniaxial tension was accompanied by extensive fragmentation of crystalline lamellae with the onset at strain e = 0.1. Limited lamellae fragmentation in the PCL/PHA composite occurred continuously over a wide range of deformations (e = 0.1–1.1) and facilitated plastic flow of the composite and was associated with the presence of a PHA nanofiber network that transferred local stress to the PCL lamellae, enforcing their local deformation. The PHA nanofibers acted as crystallization nuclei for PCL during their strain-induced melting–recrystallization. Full article

Composite hydrogels with electrospun nanofibers (NFs) have recently been used to mimic the native extracellular matrix. In this study, composite hydrogels of methacrylated hyaluronic acid containing fragmented polycaprolactone NFs were used for bone tissue engineering. The composite (NF/hydrogel) was crosslinked under ultraviolet (UV) light. The incorporation of fragmented polycaprolactone NFs increased the compression modulus from 1762.5 to 3122.5 Pa. Subsequently, adipose-derived stem cells incorporated into the composite hydrogel exhibited a more stretched and elongated morphology and osteogenic differentiation in the absence of external factors. The mRNA expressions of osteogenic biomarkers, including collagen 1 (Col1), alkaline phosphatase, and runt-related transcription factor 2, were 3–5-fold higher in the composite hydrogel than in the hydrogel alone. In addition, results of the protein expression of Col1 and alizarin red staining confirmed osteogenic differentiation. These findings suggest that our composite hydrogel provides a suitable microenvironment for bone tissue engineering. Full article