Polyaniline Nanofibers Research Articles

Elastic and layered carbon/silica composite nanofibrous aerogels through solution blow spinning

Carbon fibrous aerogels, distinguished by low density, outstanding mechanical properties and thermal stability, hold great promise for applications in aerospace, military, and environmental protection. However, large-scale production and precise structure control of carbon fibrous aerogels present significant challenges. Herein, solution blow spinning combined with rotating receiving apparatus was employed to fabricate elastic lamellar carbon/silica nanofibrous aerogels (CSNFAs). The utilization of receiving apparatus for traction enabled efficient assembly of PAN nanofiber networks into layered and stacked structure. Interlayer spacing of CSNFAs could be finely tuned within range of 30–250 μm by adjusting speed with range of 500–1000 RPM. The mesoporous architecture of CSNFAs, along with their intrinsic properties, significantly enhanced adsorption capabilities. Integration of lamellar structure enabled precise control over thermal stability. Capitalizing on laminated structure, CSNFAs exhibited excellent compressive elasticity while maintaining exceptional super elasticity across extreme temperatures ranging from 600 °C to −196 °C. CSNFAs guaranteed reliable performance across a wide temperature range and supported repeated use.

Polymer Composite Electrolytes Membrane Consisted of Polyacrylonitrile Nanofibers Containing Lithium Salts: Improved Ion Conductive Characteristics and All‐Solid‐State Battery Performance

AbstractPolymer electrolyte membranes with superior lithium‐ion (Li+) conductivity and sufficient electrochemical stability are desired for all‐solid‐state lithium‐ion batteries (ASS‐LIBs). This paper reports novel polymer composite membranes consisting of polyacrylonitrile (PAN) nanofibers (Nfs) containing lithium salts. It is first revealed that the lithium salt addition increases polar surface groups on the PAN nanofibers. Subsequently, the lithium salts‐containing PAN nanofiber (PAN/Li Nf) composite membrane affects the matrix poly(ethylene oxide) (PEO)/lithium bis(trifluoromethyl sulfonylimide) (LiTFSI) electrolyte to increase the numbers of Li+ with high mobility. Consequently, the PAN/Li Nf composite membrane shows relatively good ion conductivity (σ = 9.0 × 10−5 S cm−1) and a considerably large Li+ transference number (tLi+ = 0.41) at 60 °C, compared to the PEO/LiTFSI membrane without nanofibers. The 6Li solid‐state NMR study supports that the PAN/Li Nf bearing abundant polar nitrile groups at their surface enhances Li+ diffusion in the PEO‐based electrolyte membranes. The galvanostatic constant current cycling tests reveal that the PAN/Li Nf composite membrane possesses good electrochemical and mechanical stabilities. The ASS‐LIB consisting of the PAN/Li Nf composite membrane shows significantly improved charge and discharge cycling performances, promising future all‐solid‐state batteries.

Analysis and Application of Poly(vinyl alcohol) (PVA) and Polyacrylonitrile (PAN) Nanofiber Membrane-Based Triboelectric Nanogenerators.

The triboelectric property of materials is used to harvest energy from intentional or nonintentional sources of vibration. Contact mode freestanding dielectric based nanogenerators (CFTENGs) have many advantages when compared with other modes of triboelectric nanogenerators. The property of dielectric materials plays an important role in the energy harvesting process. In this work, we aim to fabricate nanofiber membranes of poly(vinyl alcohol) (PVA) and polyacrylonitrile (PAN) and study their properties for CFTENGs. The morphology and porosity of both membranes were tested experimentally. The mechanical property is modeled with a representative volume element (RVE) technique to understand its deflection behavior. In addition, an electromechanical model is developed to predict and analyze the behavior of those membranes in the energy conversion process. Our research reveals that the PAN dielectric layer achieves a maximum open circuit voltage of 192 kV compared to the PVA dielectric layer (2.2 kV) in the CFTENG system. In comparison, the dielectric layer of the PAN nanofiber membrane reflects its flexibility to generate electrical energy in a CFTENG with the effect of contact electrification and electrostatic induction under various sources of unused energies for a wide range of applications. Moreover, the same methodology is applied to various sources of vibration, and their performance is reported. With an appropriate power management circuit, we can design a PAN membrane-based TENG for various applications.

Arsenic removal from contaminated water using adsorptive electrospun nanofibrous membrane of polyacrylonitrile/organoclay

AbstractAdsorptive nanofiber electrospun membranes (ANEMs) show promise for heavy metal removal, particularly in dilute solutions. Nanofibrous polyacrylonitrile (PAN) membranes incorporating Cloisite 20A (C20) organoclay were fabricated via electrospinning for As(V) removal. The impact of C20 on structural properties and As(V) removal efficiency of the nanofiber membranes was investigated. The results indicated that the PAN‐C20 membranes morphology was uniform, with fiber diameters mostly falling within the 100–300 nm range. Incorporation of C20, especially in an exfoliated structure, led to increased hydrophilicity, mechanical strength, and roughness of the membranes. Batch adsorption results revealed that the adding C20 up to 1.5 wt.% significantly enhanced adsorption capacity due to the higher concentration and proper C20 dispersion. Dynamic filtration showed that the PAN‐C20(1.0) membrane achieved over 90% As(V) removal efficiency for 960 min and demonstrated excellent regeneration ability.Highlights Cloisite 20A organoclay was incorporated into PAN by electrospinning to prepare adsorptive membrane. Adsorptive membranes were used for As(V) removal from water. Type of Cloisite 20A dispersion in PAN in dynamic filtration was more important than in static adsorption PAN‐C20‐1.0 with exfoliated structure showed higher removal efficiency than PAN‐C20‐1.0 with intercalated structure. PAN‐C20‐1.0 membrane was usable for multiple adsorption–desorption cycles.

Effective oxygen evolution of NCF@CoNiO2 with one-dimensional core-shell structure synthesized by induced effect of polymer nanofibers

The non-noble bimetallic oxides have recently received more and more attention in electrocatalytic oxygen evolution reaction (OER) because of their potential to replace traditional precious metal catalysts, but the low activity and stability limit their wide application. Herein, the bimetallic oxide CoNiO2 layers are decorated on the nitrogen-doped carbon nanofibers (NCF) through in situ grown of Ni(Co) bimetal organic frameworks (Ni(Co)-MOFs) on polyacrylonitrile nanofibers and subsequent pyrolysis process, so that a new NCF@CoNiO2 electrocatalyst with one-dimensional (1D) core-shell structure is synthesized by structural induced effect of polyacrylonitrile nanofibers. Importantly, the unique interconnected network formed in the 1D NCF@CoNiO2 electrocatalyst effectively improves electron mobility and mass transport capacity, thus exhibiting the glorious OER activity and long-term stability in alkaline solutions. As a result, the optimal NCF@CoNiO2-7 electrocatalyst requires an overpotential of 518 mV for OER at the current density of 100 mA cm−2, which is obvious lower than that of RuO2 (633 mV) and CoNiO2/C-7 as a contrast sample (569 mV), respectively. This work opens up a new path for structural control of 1D bimetallic oxides to improve OER activity and stability.

Electrospun nanofibrous membranes with functionalized 2D nanofillers for efficient micropollutant removal from water

In response to emerging challenges in water pollution, such as the contamination caused by dyes and antibiotics, scientists have been driven to develop state-of-the-art remediation techniques. The electrospun nanofiber membrane effectively eliminates antibiotics and dyes from industrial wastewater. This research work primarily centres on creating electrospun membranes based on polyacrylonitrile (PAN) nanofiber membranes and mixed matrix membranes (MMM), PAN@MMM-1 and PAN@MMM-2, crafted through the electrospinning process. Enhanced membrane performance has been achieved by incorporating functionalized clay materials, alginate-bentonite (Alg-Bnt) and lanthanum-bentonite (La-Bnt) nano clay, as nanofillers. These membranes offer a combination of ease of use, high efficiency, energy and cost savings, and an environmentally friendly and ecologically beneficial nature. The study conducted a comprehensive analysis of the materials and membranes using a range of advanced technologies such as Fourier transform infrared spectroscopy (FTIR), field emission scanning electron microscopy (FE-SEM), high-resolution transmission electron microscopy (HR-TEM), energy dispersive X-ray spectroscopy (EDX), X-ray photoelectron spectrometer (XPS), X-ray diffraction spectroscopy (XRD), and the plate colony counting method for assessing antibacterial activity. UV–visible spectroscopy and HPLC were employed to determine the concentrations of antibiotics and dye compounds in the feed and permeate. The results revealed that the PAN@MMM-1 membrane exhibited a water permeability value up to 18.8 L m−2 h−1 and achieved rejection rates of up to 99.08 % for BSA, 97.82 % for cephalexin, 98.23 % for diclofenac, and 97.24 % for sulfamethoxazole. Moreover, it demonstrated impressive rejection rates of 99.39 % for methyl orange and 96.77 % for methyl violet, highlighting its remarkable efficacy in purifying wastewater.

Nanofibrous Polyacrylonitrile Membranes Coated with Nanosheets of Zn-Tetrakis(4-Carboxyphenyl) Porphyrin for Enhanced Pressure Resistance and Dye/Salt Separation

Nanofibrous Polyacrylonitrile Membranes Coated with Nanosheets of Zn-Tetrakis(4-Carboxyphenyl) Porphyrin for Enhanced Pressure Resistance and Dye/Salt Separation

Electrospun Polyacrylonitrile (PAN) Derived One Dimensional Carbon Nanofibers for Na-Ion Batteries

The desire for high performance storage devices is driven by energy demand, security and sustainability. Metal oxide based nanomaterials have limitations of high cost, poor cycle life, low yeild and structural stability. In comparison, carbon materials exhibit porous structure, work well in a wide potential window, and are highly conductive. Hence, they show enhanced rate capability and cycle life. In this work, one dimensional (1D) carbon nanofibers are synthesized with the help of electrospun PAN nanofibers as precursors. These electrospun carbonaceous nanostructures can be employed as electrodes as well as substrates, leading to structural stability after cycling and increased electrode conductivity. The morphologies and structures of as-spun nanofibers were investigated in order to develop a fundamental understanding of the nucleation and growth mechanism of carbon nanofibers. These high surface area carbon nanofibers were used as anode material for sodium (Na)-ion batteries. The electrochemical performance was first optimized in a half cell configuration. These batteries can deliver a capacity of 300 mAh g-1 at 0.1 A g-1, with cycling stability of 82% for more than >500 cycles. Thus, these electrodes can become useful in batteries beyond lithium.

P-Morpholinomethylcalix[4]arene incorporated polyacrylonitrile nanofibers as selective adsorbent for removal of Cu+2 from aqueous environment

ABSTRACT In this study, p-morpholinomethylcalix[4]arene (p-MC4) was synthesized using Mannich reaction and utilized for the fabrication of polyacrylonitrile nanofibers impregnated with p-morpholinomethylcalix[4]arene (PAN/p-MC4) using electrospinning. The nanofibers were prepared by blending 12% solution of PAN with 20% solution of p-MC4. The PAN/p-MC4 NFs were thoroughly evaluated for their removal efficiency of Cu2+ from the aqueous media. The selectivity of PAN/-p-MC4 nanofibers was also examined by adsorbing a set of metal ions with same charge and similar ionic radius. The results of distribution ratio showed that PAN/p-MC4 nanofibers have superior selectivity for Cu2+ as compared to other heavy metal ions. The relative selectivity coefficients of PAN/p-MC4 nanofibers were found to be 25.2, 14.1, 8.9, and 4.03 for Cu2+/Ni2+, Cu2+/Co2+, Cu2+/Cd2+ and Cu2+/Pb2+, respectively. This indicates that PAN/p-MC4 nanofibers have a higher selectivity for Cu2+ ions. Numerous parameters such as pH, time, adsorbent dosage and analyte concentration were optimized to evaluate the maximum adsorption capacity of nanofibers for Cu2+. Adsorption isotherm models showed that the adsorption is promising and follows Langmuir adsorption isotherm. Whereas, PAN/p-MC4 nanofibers followed pseudo- second order kinetics during adsorption experiments. The PAN/p-MC4 nanofibers showed excellent adsorption capacity (q o ) of 65.35 mg/g for Cu2+ at pH 5 in 60 min under shaking speed of 120 rpm. Moreover, PAN/p-MC4 nanofibers had been used to remove Cu2+ from real surface water samples. According to the results, PAN/p-MC4 nanofibers are more effective adsorbent for removing Cu2+ from contaminated water.

Silica Aerogel-Modified Polyacrylonitrile Nanofibers to Reduce Heat Flux in Heat Storage Tanks of Greenhouse Buildings.

Polyacrylonitrile (PAN) nanofibers have specific characteristics such as thermal insulation, weatherproofing, and sunlight resistance and therefore are appropriate to be applied as insulation materials for various industries, especially in greenhouse construction. The heat source in greenhouse buildings that operate independently in the heating network comes from heat storage tanks. In the present study, employing thermal field numerical simulations, we investigate the heat flux of a cylindrical heat storage tank with silica aerogel-modified PAN nanofibers as thermal insulation materials. The geometric scale of the tank body, thermal insulation material thickness, and outdoor temperature are optimized to improve thermal insulation. The significant discrepancy in heat flux at different parts of the heat storage tank leads to the extreme heat flux arising at the water-gas interface on the inner and outer walls. It is indicated that the heat flux distribution can be effectively ameliorated by modifying the scale of the tank body to retain the overall water temperature. In particular, effective insulation can merely be acquired when the thermal conductivity of the insulation material is below 3.3 W·m-1·K-1. Eventually, the heat storage tank is optimized to store 1400 L water at 100 °C with a radius of 0.6 m and a thermal insulation thickness of 50 mm at an outdoor temperature of -10 °C, which can maintain excellent thermal insulation for 8 and 24 h at 87.7 and 69.9 °C, respectively.

The effect of using two stabilization temperatures and fixation process on preparation of carbon nanofibers

Carbon nanofibers (CNFs) are prepared from electrospun polyacrylonitrile (PAN) because of their high carbon content. Heat treatment (oxidative stabilization and carbonization) is necessary to convert PAN nanofibers into CNFs. The fixation of fibrous structure of polymer precursor during heat treatment is always considered as a problem. The aim of this work is to study the effects of two different stabilization temperatures and fixation on CNFs prepared from electrospun PAN nanofibers. In this study, we use two different stabilization temperatures (275 and 300 °C) to investigate the effect of temperature on the oxidation, cyclization, crosslinking, aromatization, and dehydrogenation processes that occur during the stabilization heat treatment. Further, we study the effect of electrospun sheet fixation during heat treatment on the fibrous structure of electrospun fibers and methods to prevent shrinkage and folding of the electrospun sheet. Fourier transform infrared spectroscopy revealed the effectiveness of stabilization at 300 °C when transforming PAN elctrospun nanofibers to CNFs. Raman spectroscopy showed that carbonization at 800 °C after stabilization at 300 °C lowers the R-value (ID/IG ratio) comparing with that stabilized at 275 °C which indicates increasing the amount of structurally ordered graphite crystallites relative to the disordered structure. Scanning electron microscopy (SEM) revealed that fixation process maintained a uniform fibrous structure for the stabilized sheets without shrinkage, whereas carbonization at 800 °C without fixation resulted in deformed and folded carbonized PAN with loss in the fibrous structure.

Flexible Hybrid Supercapacitor Achieving 2.2V with NiCo2S4/Polyaniline/MnO2 and N, S-Co-Doped Carbon Nanofibers for Ultra-High Energy Density.

Flexible all-solid-state asymmetric supercapacitors (FAASC) represent a highly promising power sources for wearable electronics. However, their energy density is relatively less as compared to the conventional batteries. Herein, a novel ultra-high energy density FAASC is developed using nickel-cobalt sulfide (NiCo2S4)/polyaniline (PANI)/manganese dioxide (MnO2) ternary composite on carbon fiber felt (CF) as positive and N, S-co-doped carbon nanofibers (CNF)/CF as negative electrode, respectively. Initially, porous δ-MnO2 nanoworm-like network is decorated on CF using potentiodynamic method. Subsequently, interconnected PANI nanostructures is grown on the MnO2 via a facile in situ chemical polymerization, followed by the electrodeposition of highly porous NiCo2S4 nanowalls. Benefiting from 3D porous structure of conductive CF and redox active properties of NiCo2S4, PANI and MnO2, FAASC achieved a superior energy storage capacity. Later, high-performance N, S-co-doped CNF/CF negative electrode is synthesized using electropolymerization of PANI nanofibers on CF, followed by the carbonization process. The assembled FAASC exhibits a wide voltage window of 2.2V and remarkable specific capacitance of 143 F g-1 at a current density of 1 A g-1. The cell further delivers a superb energy density of 71.6Wh kg-1 at a power density of 492.7W kg-1, supreme cycle life and remarkable electrochemical stability under mechanical bending.

Nerve Regeneration Through Differentiation of Endometrial-Derived Mesenchymal Stem Cells into Nerve-Like Cells Using Polyacrylonitrile/Chitosan Conduit and Berberine in a Rat Sciatic Nerve Injury Model.

Nervous injuries are common in humans. One of the most advanced treatment methods is neural tissue engineering. This research aims to utilize nerve-like cells (NLCs) derived from endometrial mesenchymal stem cells (EnMSCs) on a polyacrylonitrile/chitosan (PAN/CS) scaffold, along with berberine, for the reconstruction of a rat sciatic nerve injury model. In this experimental study, EnMSCs were obtained through enzymatic digestion and identified using flow cytometry and their differentiation into adipocyte and osteoblast. PAN nanofiber scaffolds were produced through electrospinning, and EnMSCs were neurally differentiated on these scaffolds for grafting into an animal model. The expression of Nestin, Map-2, Tuj-1, and NF genes in NLCs was confirmed through RT-PCR and immunocytochemistry. Twenty-five adult male rats were used in this study, divided into 5 groups: (1) Scaffold/Cells/Berberine, (2) Scaffold/Cells, (3) Scaffold, (4) Berberine, and (5) Control. The animals were maintained for 8 weeks, and their sciatic nerve function (SFI) was assessed. Additionally, histological examinations were performed using hematoxylin/eosin, luxol fast blue staining, and immunohistochemistry. According to the results, extraction, identification, and differentiation of EnMSCs and fabrication of PAN conduit and its transplantation were successfully performed. The best behavioral performance and histology were observed in the Scaffold/Cells/Berberine group. The SFI test results were -24.08 for the Scaffold/Cells/Berberine group and -39.27 for the control group. The nerve diameter in these two groups was 591 µm and 80 µm, respectively, and the percentage of new nerve formation was 18.5% in the Scaffold/Cells/Berberine group and 0.2% in the control group. The immunohistochemistry results demonstrated that the intensity of the green color was higher in the groups with cells compared to the groups without cells. Furthermore, in the luxol staining results, all groups showed a significant improvement compared to the control group. In the Scaffold/Cells/Berberine group, fibers, and axons appeared denser, more organized, and displayed a higher intensity of blue staining. According to the results of this study, EnMSCs demonstrated efficient differentiation into NLCs. With the assistance of PAN/CS scaffolds and simultaneous administration of berberine, EnMSCs have the potential for nerve regeneration and recovery from sciatic nerve injury in the rat animal model.

An Electrochemical Immuno-cytosensor Modified with Nanofibers for the Determination of a Carcinoembryonic Antigen

In this study, La0.25Fe0.75FeO3 (PNp)perovskite nanoparticle was synthesized using the sol–gel method. PNp-coated polyacrylonitrile (PAN) nanofibers were prepared by electrospinning on the pencil graphite electrode (PGE) surface. In another step, carcinoembryonic antigen (CEA) was loaded with CEA antibodies (Anti-CEA) as a biomarker receptor. Finally, PGE/PAN@PNp/Anti-CEA was used for CEA detection. Optimization steps and cell culture steps were performed using differential pulse voltammetry (DPV). The use of this composite system is a novel immunosensor development approach for label-free detection of CEA. Under optimum conditions, detection limit (LOD) of PGE/PAN@PNp/Anti-CEA immunosensor LOD 1.48 ng/mL, limit of quantification (LOQ) = 4.94 ng/mL, reproducibility 1.46% (n = 5) and R2 = 0.9984 for antigen concentration within a linear working range of 0.1–10 ng/mL. Also, immunosensor recovery in real serum samples containing dopamine and ascorbic acid was found as 98.94 ± 7.43. It has great potential in clinical screening of different cancer biomarkers. The number of cells attached to the PGE/PAN@PNp/Anti-CEA/BSA(bovine serum)/CEA surface decreased in RT-4(bladder cancer), MDA-MB-231 (triple-negative breast adenocarcinoma cell line), and T98G cells (glioblastoma multiforme cell line), which are known as CEA-negative cell lines, whereas the number of MCF-7 cells (estrogen-sensitive human breast cancer cell line, known to be CEA positive) attached to the PGE/PAN@PNp/Anti-CEA/BSA/CEA surface increased, indicating higher affinity to the immunosensor surface. As a result, while MCF-7, which is CEA positive, can be determined best when using an immune-cytosensor, the cell that can be best determined with cytosensors was found to be RT-4.

Electrochemical chiral sensor developed using nanofibrous polyaniline chiral Structures: Detection and differentiation of D- and L-tryptophan

In this work, a simple strategy for electrochemical detection and differentiation of D- and L- forms of tryptophan is demonstrated using nanofibrous structures of chiral polyaniline (CP). Basically, CP with desired chirality is prepared using a chiral acid namely, ± camphor sulfonic acid (±CSA) in presence of either a cationic (or) anionic surfactant (CTAB / SDS) through a simple oxidative polymerization process. Structure, morphology and phase purity of the resultant CP materials are characterized by field emission scanning electron microscopy, Fourier transform infrared spectroscopy, Raman spectroscopy and X-ray diffraction studies. Moreover, the chiral properties of these conducting polymers are evaluated using circular dichroism (CD) spectroscopic studies. From these analyses it is found that CP exhibited twisted nanofibrous morphology and possesses the chirality whereas the non-chiral polyaniline (PANI), prepared in the absence of chiral acid, displayed the formation of a simple fibrous structures without any twists or chirality. Interestingly, such CP materials are found to be electrochemically selective for the detection and differentiation of D- and L- forms of tryptophan (Trp). Among the different chiral materials, CP-CT(−) prepared using CTAB displayed a much better sensing characteristics with higher IL/ID ratio, wider concentration range of detection and lower detection limit of 0.98 µM for l-Trp and 1.2 µM for d-Trp respectively. On the other hand, non-chiral PANI does not display any sensing behavior towards the differentiation of amino acid, Trp. Further, chronoamperometric studies reveal the selectivity of this chiral sensor for the detection of Trp among the other potentially interfering analytes. Although the difference in the measured peak current value is smaller, a significant difference of 70 mV peak potential is observed for the differentiation of L- and d-Trp. Moreover, the proposed CP-based sensing platform exhibits excellent stability and reproducibility with statistically negligible error values suggesting the potential use of the developed material towards electrochemical chiral detection and differentiation of amino acid, Trp.

Dynamic Spectral Metafabric with Unidirectional Moisture Transport Property for Personal Thermal Management.

Personal thermal management technology, which adjusts the heat exchange between the human body and the environment, can passively heat or cool the body to maintain a comfortable core temperature, thereby enhancing comfort and reducing energy consumption. However, most existing personal thermal management materials have static properties, such as fixed solar reflectance and infrared emissivity, which do not support real-time dynamic temperature regulation. Moreover, sweat accumulation on the skin surface, while contributing to temperature regulation, can significantly reduce comfort. This study constructs a unidirectional moisture-permeable intelligent thermal management fabric system to achieve superior thermal and moisture comfort in complex environments. The fabric incorporates thermochromic microcapsules into PAN nanofibers by using electrospinning technology for intelligent thermal management. Subsequent hydrophobic treatment of the fiber film surface imparts the fabric with unidirectional wetting properties. The nanofibrous structure provides intrinsic elasticity and breathability. In heating mode, the fabric's average sunlight reflectance is 42.1%, which increases to 82.2% in cooling mode, resulting in a reflectance difference of approximately 40%. The hydrophobic treatment endows the fabric with excellent moisture absorption and perspiration properties, demonstrated by a unidirectional moisture transport index of 696.63 and a perspiration evaporation rate of 5.88 mg/min. When the fabric temperature matches the ambient temperature, the photothermal conversion power difference of the Janus metafabric in two modes reaches 248.37 W m-2. Additionally, Janus metafabrics show the potential for temperature-responsive design and repeated writing applications. The outstanding wearability and dynamic spectral properties of these metafabrics open new pathways for sustainable energy, smart textiles, and thermal-moisture comfort applications.

Centrifugally spun hydroxyapatite/carbon composite nanofiber scaffolds for bone tissue engineering

In recent years, advancements in tissue engineering have demonstrated the potential to expedite bone matrix formation, leading to shorter recovery times and decreased clinical challenges compared to conventional methods. Therefore, this study aims to develop composite carbon nanofibers (CNFs) integrated with nano-hydroxyapatite (nHA) particles as scaffolds for bone tissue engineering applications. A key strategy in achieving this objective involves harnessing nanofibrous structures, which offer a high surface area, coupled with nHA particles expected to accelerate bone regeneration and enhance biological activity. To realize this, polyacrylonitrile (PAN)/nHA nanofibers were fabricated using the centrifugal spinning (C-Spin) technique and subsequently carbonized to yield CNF/nHA composite structures. Scanning Electron Microscopy (SEM) confirmed C-Spin as a suitable method for PAN and CNF nanofiber production, with nHA particles uniformly dispersed throughout the nanofibrous structure. Carbonization resulted in reduced fiber diameter due to thermal decomposition and shrinkage of PAN molecules during the process. Furthermore, the incorporation of nHA particles into PAN lowered the stabilization temperature (by 5 °C–20 °C). Tensile tests revealed that PAN samples experienced an approximately 80% increase in ultimate tensile strength and a 187% increase in modulus with a 5 wt.% nHA loading. However, following carbonization, CNF samples exhibited a 50% decrease in strength compared to PAN samples. Additionally, the addition of nHA into CNF improved the graphitic structure. The incorporation of nHA particles into the spinning solution represents a viable strategy for enhancing CNF bioactivity.

Fe3O4@CNTs/PANI/PI fabric with magnetic–dielectric nanonetwork as a highly efficient microwave absorber

Since the matching between the complex permittivity and permeability plays a dominant role in the performance of microwave absorbing, magnetic-dielectric materials have been increasingly used for microwave absorption. In this paper, Fe3O4 nanoparticles anchored on carbon nanotubes (Fe3O4@CNTs) were fabricated via a self-assembled technique. The efficient microwave-absorbing fabric was synthesized by building polyaniline nanofibers (PANI NFs) and Fe3O4@CNTs magnetic–dielectric network on the surface of polyimide (PI) fabric. The results of SEM, FTIR, and XRD demonstrated the presence of Fe3O4@CNTs on the fabric surface. The decomposition temperature (Td) of the fabric was beyond 580.0 °C and the fabric exhibited strong hydrophobicity (water contact angle 125.0°). The Fe3O4@CNTs/PANI/PI fabric possessed a minimum reflection loss (RL) value of −62.61 dB (>99.9 % absorption) with a matching thickness of 1.58 mm. The excellent microwave absorption capacity is attributed to the well impendence match, dielectric and magnetic loss, and the scattering loss of the special cell structure.

Deposition of polyaniline nanofibers on activated carbon textile for high-performance pseudocapacitors

Deposition of polyaniline nanofibers on activated carbon textile for high-performance pseudocapacitors

Electrochemical degradation of small molecule dyes by TiO2-decorated polyacrylonitrile nanofiber membranes with superior properties

To optimize the uniform dispersion of nanoparticles and enhance their catalytic degradation effect on small molecule dyes in textile wastewater, titanium dioxide (TiO2) was deposited on polyacrylonitrile (PAN) fiber membranes using magnetron sputtering technology, and TiO2/PAN nanofiber membrane (NFM) with low content and high catalytic efficiency was successfully prepared. Through membrane separation coupling electrocatalysis, the composite membranes exhibited outstanding performance in removing Congo red (CR), Sunset yellow (SY), Methyl orange (MO), and Methylene blue (MB) dyes, with removal rates of 99.5%, 98.8%, 98.5%, and 87.2% respectively. Even after continuous catalysis for 10 h, the composite membranes maintained a high dye removal rate, demonstrating their remarkable stability and water treatment capabilities. Furthermore, TiO2/PAN NFMs displayed high pure water permeance, dye permeance, and mechanical strength. Specifically, M20 (magnetron sputtering time of 20 min) showed water permeance and dye (SY) permeance values of 1944 L·m−2·h−1·bar−1 and 816 L·m−2·h−1·bar−1, respectively, and indicate superior mechanical and electrochemical properties. During the electrocatalytic process, TiO2/PAN NFMs generated reactive oxygen species (ROS) on the surface, imparting a self-cleaning property that extended the service life of the membranes and offered an effective solution for textile wastewater treatment.