Search Results (513)

Electrochemical oxidation (EO) possesses numerous advantages and great potential for organic pollutant degradation. However, traditional plate anodes for EO are limited by pollutant mass transfer, leading to low oxidation efficiency and high energy consumption. Herein, a three-dimensional (3D) polyacrylonitrile-based carbon fiber brush (PAN-CFB) anode was employed to enhance mass transfer and improve oxidation efficiency. The oxidation capacity of the PAN-CFB anode was compared with those of boron-doped diamond (BDD) and Ti/IrO₂-Ta₂O₅ plate anodes using oxalic acid (OA), phenol, and perfluorooctanoic acid (PFOA) as target pollutants, respectively. Experimental results demonstrated that the 3D PAN-CFB anode exhibits superior direct oxidation capacity compared to BDD and the Ti/IrO₂-Ta₂O₅ plate anode in degrading OA, which is attributed to the significantly enhanced mass transfer of OA toward the brush anode surface. Under a constant current of 400 mA for 240 min, the total organic carbon (TOC) removal from 50 mmol/L OA reached 90.5%, 57.5% and 6.6% for PAN-CFB, BDD and the Ti/IrO₂-Ta₂O₅ anode, respectively, and the energy consumption followed the order of PAN-CFB (5.5~8.9 kWh/kg_TOC) < BDD (11.2~19.3 kWh/kg_TOC) < Ti/IrO₂-Ta₂O₅ (76.1~120.7 kWh/kg_TOC). However, the 3D PAN-CFB anode exhibited poor stability at high potential and failed to promote phenol and PFOA degradation due to the weak direct oxidation capacity toward the two pollutants and the poor generation capacity of reactive oxygen species, associated with its low oxygen evolution potential. Therefore, future efforts should focus on developing stable 3D brush electrodes with a higher oxygen evolution potential to enable non-selective oxidation of a broader range of pollutants. Full article

Due to the constant need to develop biocompatible materials with osteoconductive and osteoinductive properties, the main objective of this study was to evaluate and characterize the carbon fiber obtained from fiber polyacrylonitrile textile carbon fiber (PAN), in the different forms: non-activated carbon fiber felt (NACFF) and activated carbon fiber felt (ACF) with silver (Ag-ACF), gold (Au-ACF), copper (Cu-ACF), palladium (Pd-ACF) and platinum (Pt-ACF), on the cell behavior and osteogenesis of mesenchymal cells. For characterization: scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS) and Raman analysis. In vitro analysis was performed on rat mesenchymal stem cells. For each experimental group, 5 wells (n = 5) were made where cell proliferation (CP): cell viability (CV), mineralization nodule formation (MNF), total protein content (PT) and alkaline phosphatase activity (APC) were quantified, and cell morphology was analyzed by direct fluorescence, genotoxicity and cell interaction by SEM. The data passed the normality test and was followed by the one-way ANOVA test, followed by the Tukey test, using the conventional significance level of 5%. All the samples were statistically similar in terms of cell proliferation, except for the Ag-ACF group in relation to the control group (C). For cell viability, C obtained greater viability than the other groups, while ACF obtained a statistical difference and was superior to the Ag-ACF, Cu-ACF, Pt-ACF groups, being statistically similar to the Au-ACF and Pd-ACF groups. In the evaluation of ACP, the Ag-ACF and Cu-ACF groups were lower than the C, and other groups; for the characterization tests Au-ACF and Pd-ACF showed a more homogeneous metal distribution compared to the other groups. Cu-ACF and Ag-ACF showed some toxicity and low induction of osteoblastic differentiation. Although platinum showed relative cellular viability, a high micronucleus count was reported for this ion. In conclusion, ACF has the potential to be developed as a future biomaterial with good cell viability. Carbon fibers incorporated with gold and palladium ions showed potential for future application as supports for bone repair. Full article

Microplastics (MPs) are emerging pollutants that affect soil–microbe interactions in paddy ecosystems. Periphytic biofilms (PBs) are complex microbial consortia that ubiquitously distribute at the soil–water interface of paddy ecosystems, playing essential roles in nutrient cycling and pollutant migration. However, whether MPs affect the community composition of PBs remains largely unknown. This microcosm study investigated the effects of three types of MPs (polyacrylonitrile, PAN; polyethylene, PE; and polyethylene terephthalate, PET) on the community characteristics of PBs via high-throughput sequencing (16S/18S rRNA) technology. Results showed that the addition of all MPs significantly increased the biomass and chlorophyll-a content of PBs, with PAN inducing the maximum increase (by 331.9% and 128.6%). However, all MPs had no significant effect on the PB α-diversity of bacterial and eukaryotic communities (p > 0.05). As for PB composition, PAN and PET increased the relative abundance of Cyanobacteria, Proteobacteria and Holozoa, PE increased that of Cyanobacteria, Bacteroidota and Blastocladiomycota, and all MPs decreased the relative abundance of Chloroflexi, Actinobacteriota and Basidiomycota. Furthermore, PET decreased the predicted functional potential of natural polymer degradation (cellulolysis, ligninolysis, xylanolysis, ureolysis), nitrogen fixation and nitrate ammonification, while PE increased predicted potential for plastic degradation, nitrate reduction and denitrification. Co-occurrence network analysis suggested that the PE network showed higher connectivity and lower modularity, while the PAN network showed higher modularity. This study advances our understanding of soil MPs–microbe interactions under high-concentration conditions. It also suggests that PB community characteristics may serve as potential bioindicators for soil MP pollution. Full article

Conductive hydrogels are attractive for flexible electronics, but their practical use is often limited by resistance drift during repeated deformation and performance degradation at low temperatures. Here, core–shell polyaniline-coated polyacrylonitrile (PANi@PAN) electrospun nanofibers were incorporated into a polyacrylamide/hydroxypropyl cellulose (PAM/HPC) hydrogel matrix to construct a hybrid conductive network. The PANi shell serves as an electronic pathway alongside ionic conduction in the hydrated polymer network, leading to markedly improved electromechanical stability. The resistance drift is about 11% after 2000 stretching–relaxation cycles at 0–100% strain, about 12 times lower than that of the nanofiber-free hydrogel. Stable electrical responses are maintained under large deformation, with a resistance drift as low as 3.3% over a strain range of 0–400%. The hydrogels show a conductivity of 0.32 S m⁻¹ while retaining high stretchability (>600%). An ethylene glycol/water binary solvent is used to suppress ice formation and improve moisture retention, allowing stable electromechanical performance at −15 °C over 500 cycles. The hydrogel also adheres reliably to human skin (about 10.25 kPa) and functions as a conformal strain sensor without extra fixation. Full article

Over the past decades, plastics have been increasingly employed to package foods and beverages. Furthermore, foods, nowadays, are kept in contact with plastics for far longer periods than ever before. A number of conventional polymers, i.e., polyethylene (PE), Polypropylene (PP), Ethylene Vinyl Acetate (EVA), Εthylene vinyl alcohol (EVOH) polystyrene (PS), Polyvinyl chloride (PVC), Polyvinylidene chloride (PVDC), polyethylene terephthalate (PET), Polycarbonate (PC), polyethylene naphthalate (PEN), Polyamides (PAs), Polyacrylonitrile (PAN) as well as biodegradable polymers-[Polylactide (PLA)] are used commercially in food packaging applications. Potential interaction of food with the packaging container includes: permeation, migration and flavor scalping. Most food and beverage containers are lined with plastics mainly polyolefins, which due to their low polarity tend to absorb volatile compounds of similar polarity. Absorption of flavor compounds by polymers involves both partitioning and diffusion through the plastic. Absorption is influenced by (i) polymer properties such as polarity, morphology, glass transition temperature, density, free volume, crystallinity and surface area, (ii) flavor compound properties such as structure, concentration, and polarity, and (iii) external factors such as temperature, time of contact, relative humidity and the proximity of other compounds. Based on the above, it is apparent that flavor scalping should be among one of the food packaging industry priorities in order to efficiently preserve the quality of packaged food flavor. This review highlights the various factors affecting the scalping process, as well as the consequences of flavor scalping in various food and beverage commodities. The review covers the period 1990–2925 and used the LitChemPlast data base for literature search. Full article

This study reports the development and characterization of hierarchical electrospun scaffolds based on poly (L-lactic acid) (PLA) and polyacrylonitrile (PAN) reinforced with calcium oxide (CaO) nanoparticles (18.5 ± 4.7 nm) for skin regeneration. Six configurations, including two five-layer multilayer systems (PLA/PAN/CaO and PAN/PLA/CaO), were evaluated to determine how composition and deposition sequence influence physicochemical, mechanical, and biological performance. FT-IR, XRD and DSC confirmed the successful integration of CaO, while thermal analysis evidenced an effect of chain mobility and interfacial interactions within multilayer systems. Cross-sectional SEM revealed the presence of both fibers with continuous interfaces. Nitrogen adsorption showed that CaO significantly increased the specific surface area (e.g., from 4.6 m²/g in neat PLA to 21.65 m²/g in PLA/CaO), with type IV isotherms indicating mesoporosity. Wettability assays demonstrated reduced contact angle in PLA (from 126.3° to 91.8°) and sequence-dependent surface properties in multilayers. Tensile testing confirmed that the multilayer architecture bridged the mechanical gap between compliant PLA and high-strength PAN, yielding intermediate moduli (~10–11 MPa) and balanced toughness. Antibacterial assays against S. aureus and E. coli showed that CaO significantly reduced bacterial viability, with PLA/PAN/CaO achieving the highest inhibition (up to 37.1%). In vitro HaCaT assays and in vivo implantation in BALB/c mice confirmed high cytocompatibility and biocompatibility. These findings demonstrate that multilayer electrospinning of PLA/PAN/CaO enables the design of structurally integrated, bioactive, and mechanically balanced scaffolds for advanced wound healing and dermal repair. Full article

In this study, a composite powder explosion suppressant (MVTS–NaHCO₃) was prepared via the wet coating method of the solution–crystallization (WCSC) process, using modified vanadium–titanium slag (VTS) as the carrier and NaHCO₃ as the active suppressive component. A 20 L spherical explosion apparatus and a transparent pipeline explosion propagation test system were employed to investigate the effects of the composite powder explosion suppressant with different mass fractions (0%, 10%, 20%, 30%, 40%, 50%) on the explosion pressure and micro-mechanism of polyacrylonitrile (PAN) dust. The experimental results indicated that the MVTS–NaHCO₃ composite powder exhibited a significant suppression effect on PAN dust explosions. In the confined 20 L vessel, complete suppression was achieved when the mass fraction of the composite powder explosion suppressant exceeded 30%, with a maximum explosion pressure reduction of 53.2%. In the semi-open pipeline, 40% composite powder explosion suppressant reduced the maximum explosion pressure to 0.08 MPa (a reduction rate of 82.6%), and complete suppression was achieved at a mass fraction of 50%. Microstructural analysis revealed that the suppression performance of the composite powder explosion suppressant is attributed to the synergetic effects of physical and chemical mechanisms. Physically, NaHCO₃ decomposes endothermically (100 kJ/mol), releasing CO₂ and H₂O and thereby diluting the oxygen concentration, while the porous structure of MVTS enhances dispersibility. Chemically, the hydroxyl groups on the surface of MVTS bond with NaHCO₃, delaying its decomposition, while metal hydroxides (e.g., Al(OH)₃) decompose thermally to form Al₂O₃, which adsorbs and quenches free radicals (e.g., ·OH, ·H), thereby inhibiting chain reactions. This study provides new insights for the resource utilization of VTS and the prevention and control of industrial dust explosions. The findings have important reference value for optimizing explosion suppressant formulations and improving the intrinsic safety. Full article

To reduce the production cost of ultra-high performance concrete (UHPC), this study incorporated polyacrylonitrile (PAN) fibers and coarse aggregates (CA) to develop a novel UHPC with both excellent performance and reduced cost. A two-stage mortar-concrete design approach was employed to optimize the UHPC mix proportion. First, the mortar matrix was preliminarily optimized based on particle packing theory, and its strength development mechanism was analyzed. Subsequently, response surface methodology was applied to systematically investigate the effects of PAN fiber content, CA content, and superplasticizer (SP) dosage on the slump flow, compressive strength, flexural strength, indirect tensile strength, freeze–thaw resistance, and dynamic mechanical properties of UHPC. The entropy weight method was then adopted to determine the optimal mix proportion, followed by cost estimation. The results indicate that the optimal mortar matrix composition consists of 61.4% cement, 15% silica fume, and 23.6% fly ash, achieving a flow spread of 246 mm, a compressive strength of 117.2 MPa, and a flexural strength of 24.9 MPa. When the PAN fiber content, CA content, and SP dosage were 0.5%, 20%, and 3.8%, respectively, the prepared PAN-CA UHPC(PCUHPC) exhibited the best overall performance. Compared with conventional UHPC, the material cost was reduced by 81.7%, and the compressive strength-normalized cost decreased by 75.4%. The UHPC developed in this study, characterized by outstanding performance and significant cost advantages, provides a feasible solution and theoretical support for broader engineering applications. Full article

A flexible polyionic liquid (PIL) nanofiber membrane-supported phosphomolybdic acid catalyst (PM-PIL) was fabricated via stepwise chemical transformation of polyacrylonitrile (PAN) nanofiber membranes. The nitrile groups of PAN were converted into pyridine units, followed by quaternization and anion exchange with phosphomolybdic acid (PMo), resulting in a polyionic liquid membrane with uniformly immobilized PMo species. Benefiting from its nanofibrous architecture and ionic liquid characteristics, the PM-PIL membrane simultaneously acts as a heterogeneous catalyst and a Pickering emulsion stabilizer, enabling efficient interfacial catalytic oxidation desulfurization. The PM-PIL membrane exhibited excellent catalytic performance toward dibenzothiophene (DBT) oxidation in an H₂O₂-based model oil system. Under optimized conditions (60 °C, O/S = 150:1), more than 90% DBT removal was achieved within 90 min, and complete desulfurization was obtained within 2 h. Compared with phosphomolybdic acid and poly(pyridine), the PM-PIL membrane showed markedly enhanced activity and stability, maintaining over 90% efficiency after six cycles. Product analysis confirmed selective oxidation of DBT to dibenzothiophene sulfone. This work provides a robust and recyclable membrane-based catalytic platform for efficient oxidative desulfurization. Full article

The growing demand for wearable electronics and the Internet of Things (IoT) calls for flexible piezoelectric energy harvesters with substantially improved power output. Polyacrylonitrile (PAN) polymers, with their high polarization and excellent thermal stability, are among the most promising candidates for efficient flexible piezoelectric materials. However, the performance of existing PAN-based harvesters remains limited, and strategies for further enhancing their output are still insufficiently explored. Herein, this study aims to overcome the output bottleneck of PAN-based PENGs by implementing a novel mechanical excitation strategy. Using electrospun flexible PAN-BaTiO₃ nanocomposite films, we systematically compared the electromechanical responses under conventional compression and impact modes. Real-time synchronized force–current measurements in compression mode revealed that the output current increases progressively with drive frequency (2–10 Hz). Specifically, the PENG with PAN-20 wt.% BaTiO₃ achieved a peak current of 0.33 mA at 10 Hz, showing an approximately 7.9-fold enhancement over its pure PAN counterpart. More importantly, under 6 Hz impact excitation, the device exhibited a remarkable output current density of 1.0 mA cm⁻² and a peak power density of 256.5 µW cm⁻². This current density is 95 times higher than that in compression mode at a comparable frequency and surpasses the performance of most recently reported piezoelectric and triboelectric nanogenerators. With an effective area of 16 cm², the PENG could simultaneously illuminate up to 275 commercial LEDs or 100 individual bulbs and maintained stable operation over 63,530 cycles. This work overcomes the output bottleneck in low-frequency energy harvesting and provides an effective pathway toward practical energy-harvesting applications. Full article

A novel polycationic membrane (PCM) was synthesized by the cyclization of polyacrylonitrile (PAN) with m-ethylene diamine, converting the nitrile groups into pyridine units, followed by quaternization with 1-bromobutane. The resulting PCM was further functionalized by loading the photocatalyst, phosphomolybdic acid (PMo), via anion exchange, forming a new type of photocatalytic material, PM-PCM. Under visible light irradiation, the PM-PCM photocatalyst achieved an impressive methylene blue degradation rate of 98%. Additionally, the nanofiber membrane morphology facilitates the efficient recovery of the catalyst, with 98% of the initial degradation efficiency maintained after five photocatalytic cycles. This robust, highly efficient, and recyclable material provides a new approach for catalyst support. To the best of our knowledge, PM-PCM is the first reported photocatalyst of this kind. This cost-effective, functionalized membrane material utilizes solar light as an economical and clean energy source, offering promising potential for sustainable environmental applications. Full article

Physically triggered drug release is an emerging field focused on developing materials capable of modulating release kinetics in response to external stimuli. In this work, we present a strategy for the fabrication and evaluation of heat-mediated drug release from electrospun fibers composed of a polyacrylonitrile (PAN) and poly (methyl vinyl ether-alt-maleic acid) (PMA-MVE) blend, encapsulating vitamin B₁₂ (B₁₂-NFs) as a model. Following thermal treatments at 90, 120, and 180 °C, results from SEM, TGA, DSC, and FTIR confirmed that increasing the crosslinking temperature promoted the formation of a more hydrophobic matrix (contact angle > 150°), which effectively reduced spontaneous drug leakage. As a proof-of-concept, we evaluated the sensitivity of the elaborated B₁₂ to heating in aqueous media using UV-Vis spectrometry. The results indicate that the release kinetics followed a sigmoidal profile governed by the dissolution Gompertz model. This laboratory-scale evaluation establishes the fundamental mechanisms for magnetically triggered platforms based on polymeric blends, providing a robust framework for the design of remotely activated, non-invasive drug delivery platforms. Full article

We present an investigation to develop innovative composite fibrous electrodes optimized for a supercapacitor with a “green” low-cost aqueous electrolyte, superconcentrated potassium formate, which raises the maximum energy storage device voltage beyond the water electrolysis limit. Three types of electrospun nanofiber mats are investigated for optimum pseudocapacitance with this electrolyte: polyaniline (PANI)/polyacrylonitrile (PAN) fibers, without or with 1 wt% or 10 wt% graphene nanoplatelets (GNP). These nanofiber mats are considered as standalone electrodes or in bilayer formations with a phenolic-derived activated carbon fabric. Supercapacitor cells with these electrodes are tested electrochemically via electrical impedance spectroscopy, cyclic voltammetry and galvanostatic charge–discharge at different current densities. The supercapacitor with hybrid electrode bilayers of activated carbon fabric and electrospun fiber mat consisting of PANI:PAN at 50:50 w/w with 10 wt% GNP exhibited the best performance with an energy and a power density of 39 Wh/kg and 6057 W/kg of electrodes, respectively. Full article

Gel polymer electrolytes (GPEs), which combine the safety of solid electrolytes with the high ionic conductivity of liquid electrolytes, have long been regarded as ideal electrolyte materials. This study proposes a polymer/ceramics composite gel electrolyte aimed at improving the performance of lithium-ion batteries. A nanofiber membrane was fabricated by electrospinning a mixture of polyacrylonitrile and lithium-salt-grafted helical mesoporous silica nanoparticles, followed by plasticizer absorption to obtain the composite gel electrolyte film (PAN/SiO₂-Li). Experimental results indicate that this gel electrolyte membrane possesses high thermal stability, a wide electrochemical window (>5.3 V vs. Li/Li⁺), high room-temperature ionic conductivity (~4.4 × 10⁻³ S cm⁻¹), and a good lithium-ion transference number (0.72). In symmetric Li||Li cells, this electrolyte suppresses lithium dendrite growth and maintains stable lithium deposition/stripping. This work presents a practical electrolyte design strategy for developing GPEs with enhanced safety and performance. Full article

Fine-denier silicone emulsions play an important role in the polyacrylonitrile (PAN) precursor treatment process by reducing surface tension and preventing fiber fusion during thermal stabilization and carbonization. These emulsions are typically prepared by dispersing polydimethylsiloxane (PDMS) polymers with various functional groups into water through different emulsification methods. In this study, two types of silicone emulsions—one prepared using a mechanical disperser and the other using a high-shear colloid mill—were manufactured on a pilot scale and systematically compared. Thermal aging was conducted at 50 °C and 70 °C for approximately one month, and changes in particle size, dispersion stability, and physicochemical properties were evaluated. The colloid-mill emulsification method produced smaller and more uniform silicone particles and exhibited superior thermal and dispersion stability relative to the mechanically dispersed emulsion. NMR relaxation, Turbiscan multiple light scattering, and viscosity measurements confirmed that the colloid-mill emulsion maintained a stable microstructure with minimal aggregation even under elevated-temperature storage. These results demonstrate that high-shear emulsification is an effective approach for producing fine-denier silicone emulsions with enhanced stability, making the colloid-mill method a more reliable and practical route for preparing silicone-based oiling agents used during PAN precursor processing in carbon fiber manufacturing. Full article