Search Results (2,766)

The exposure of microplastics (MPs) to ultraviolet (UV) light in the environment can affect their flotation behavior and removal efficiency. This study investigated the effects of UVC irradiation on the physical and surface characteristics of polypropylene (PP), polyethylene (PE), acrylonitrile butadiene styrene (ABS), polystyrene (PS), polyethylene terephthalate (PET), and polyvinyl chloride (PVC), and evaluated their removal using agglomeration–micro-flotation. MPs were irradiated with UVC for 7 days, and they were characterized using particle size distribution analysis, CIE L*a*b* color analysis, and contact angle measurements. Flotation experiments were conducted using kerosene as a hydrophobic bridging liquid. The results showed that UVC irradiation induced polymer-dependent changes, including fragmentation, apparent shape-related changes, and redistribution behavior, resulting in changes in particle size distribution. Surface discoloration and reduced contact angle were also observed after UV exposure, suggesting photooxidative surface modification and increased surface hydrophilicity. These surface modifications reduced flotation performance at low kerosene dosages, particularly for PET and PVC. However, increasing kerosene dosage improved removal efficiency by enhancing agglomeration and particle–bubble attachment. The results indicated that agglomeration–micro-flotation is a promising approach for removing UV-aged MPs and provided insights into the influence of UV-induced surface modifications on flotation behavior. Full article

Ionogels combining ionic liquids with polymer networks show promise for flexible electronics, but their mechanical and functional performance often needs enhancement. Here, we report a series of magnetic nanocomposite ionogels fabricated by doping triiron tetraoxid (Fe₃O₄) nanoparticles into a [C₂mim]⁺[EtSO₄]⁻-dispersed cross-linked PAA matrix. The effect of PAA content (10–20 wt%) on the optical, mechanical, and dielectric properties of pure imidazolium ionogels was first investigated. Increasing PAA concentration enhanced tensile strength (up to ~0.7 MPa) and compressive modulus (~0.65 MPa) while reducing optical transmittance; dielectric relaxation peaks around 6–8 GHz were observed, with the 15 wt% sample showing the highest permittivity. Subsequently, Fe₃O₄ nanoparticles (0–20 wt%) were incorporated into the 10 wt% PAA ionogel. The resulting magnetic ionogels exhibited reduced tensile strength, but significantly increased elongation (up to ~12 strain), indicating network softening. Magnetic hysteresis measurements confirmed superparamagnetic behavior with saturation magnetization reaching ~2.5 emu/g at 20 wt% Fe₃O₄ loading. This work demonstrates a facile strategy to simultaneously tune mechanical, dielectric, and magnetic properties in imidazolium ionogels, providing guidelines for designing soft multifunctional materials for microwave absorption, magnetic actuation, and flexible sensor applications. Full article

To address prevalent industrial challenges, including the high cost of fabricating microstructures via photolithography and 3D printing, impurity residues easily generated by conventional physical/chemical pore-forming techniques, and the limited sensitivity of regular capacitive sensors, this paper innovatively proposes an integrated low-temperature in situ gas foaming strategy using ammonium bicarbonate for the fabrication of porous TPU-based ionic gels. Relying on the complete gaseous decomposition property of ammonium bicarbonate upon heating, a three-dimensionally interconnected continuous porous network is spontaneously constructed inside the polymer matrix. Thermoplastic polyurethane (TPU) is selected as the continuous polymer phase, and [EMIM][TFSI] imidazolium ionic liquid is blended as the ion source to synthesize composite ionic gel substrates. A PDMS composite slurry filled with graphene is employed to prepare flexible substrates, followed by low-temperature oxygen plasma surface modification to introduce polar functional groups such as hydroxyl and carboxyl onto electrode surfaces. A standard sandwich-structured ionic pressure sensor with the configuration of “top modified electrode—porous ionic gel dielectric layer—bottom modified electrode” is finally assembled. The porous framework and modified electrodes constitute a dual synergistic enhancement system: the porous structure markedly reduces the equivalent elastic modulus of the gel and improves its compressive deformation capacity; polar-modified electrodes optimize the interfacial compatibility between electrodes and gels, shorten ion migration paths and lower interfacial contact resistance. Systematic calibration of multiple batches of parallel samples reveals that the as-fabricated sensor achieves a high sensitivity of 25.3 kPa⁻¹ across the full measuring range from 0 to 1000 kPa with a linear fitting coefficient R² = 0.992. The loading response time and unloading recovery time of the device are 60 ms and 80 ms respectively, with a performance degradation of less than 3% after 1000 consecutive loading–unloading cycles, featuring low hysteresis error and excellent signal repeatability. Multi-scenario in vivo wearable tests on human subjects verify that the device can precisely capture subtle fluctuations of radial artery pulse and periodic laryngeal deformation during swallowing, distinguish characteristic waveform patterns of various English words according to differences in vocal cord vibration, and accurately detect bending motions when attached to finger joints. The entire fabrication process adopts common chemical raw materials and standard laboratory equipment without expensive micro-nano processing facilities, featuring convenient raw material procurement and high process fault tolerance, which enables large-area coating-based mass production. This work delivers a novel technical route for the low-cost large-scale production of high-performance ionic flexible sensors and bears significant industrialization reference value for applications in wearable medical monitoring, bionic robotic electronic skin, flexible human–machine interactive touch panels and other related fields. Full article

Usually, particle morphology and surface treatment are adjusted to achieve high conductivity in highly filled conductive polymer composites. Here, we demonstrate that this key property can be further improved by keeping the particle contact regions free of polymer using an extension of the capillary suspension concept. If the secondary liquid is chosen such that it remains in the contact areas between conductive particles during solidification of the polymer phase, then the composite conductivity substantially increases. For both a thermoset and a thermoplastic model system including 40 vol.% silver particles in the paste, the conductivity was more than doubled compared to the respective binary system, reaching conductivity values up to (4.3 ± 0.2) × 10⁶ Sm⁻¹. SEM images clearly show the polymer-free contact regions in samples with enhanced conductivity. However, conductivity only increases if the secondary fluid is removed after solidification of the polymer phase. Thus, the capillary suspension concept can be used for a controlled modification of particle–particle contacts and represents a generic, viable strategy for enhancing conductivity in highly filled polymer composites. The concept helps to save precious (silver) resources and may find application in various fields of printed electronics, e.g., metallization of thermosensitive solar cells. Full article

Icing phenomena on wind turbine blades and components are a major problem, causing downtimes that increase maintenance costs, reducing the blade’s lifespan, or in severe cases, even leading to component damage. A nanofiber-based bi-layer liquid-infused surface (BLIS) coating was prepared and characterized, combining good adhesion to wind turbine blades with low ice adhesion. The BLIS coating was produced by a new method combining electrospinning and a heat treatment step, containing a poly ethyl-2-cyanoacrylate (PECA)-based adhesive layer, a slippery layer of poly vinylidene fluoride-co-hexafluoropropylene (PVDF-HFP) copolymer, and an infiltrated perfluoropolyether lubricant. Thermogravimetric analysis (TGA) was used to ensure the thermal stability of the polymers in the nanofiber coating layers and to optimize the heat treatment process of the layers. Microstructural changes were studied by scanning electron microscopy (SEM) and surface roughness measurements. Contact angle measurements and sliding velocity tests on wind turbine blade segments at icing conditions of 0 °C and +5 °C indicate that the water sliding properties of the BLIS coating were improved compared to uncoated blades. In addition, coated blade segments showed a 50% lower ice adhesion strength than uncoated blades. Full article

Deep unconventional oil and gas reservoirs are critical to hydrocarbon exploration and development in China. However, their complex geological and petrophysical features, including high temperature, high pressure, high salinity, multiple pressure systems, and intricate pore–fracture structures, make them highly susceptible to formation damage during drilling, completion, stimulation, and production. Effective reservoir protection is therefore essential for minimizing damage and improving development efficiency. This paper systematically reviews recent advances in reservoir protection for deep unconventional reservoirs, with a focus on evaluation methods and protective materials. Laboratory evaluation methods, including permeability recovery, nuclear magnetic resonance, pressure decay, and spontaneous imbibition, together with field-based approaches such as well testing and production decline analysis, are summarized and assessed for their applicability to complex damage characterization. Major damage mechanisms, including liquid-phase trapping, solid invasion, sensitivity damage, stress sensitivity, and wettability alteration, are analyzed with emphasis on working fluid–reservoir interactions under multi-field coupling conditions. Recent progress in protective materials is also reviewed, covering polymer-based materials such as gel sealing agents, delayed-swelling hydrogels, water-/oil-soluble temporary plugging agents, and film-forming polymers, as well as ultrafine CaCO₃ and fiber-based materials. In addition, related protection technologies, including temporary plugging, film-forming fluid-loss control, underbalanced drilling, and low-damage completion fluids, are discussed. Existing models developed for conventional sandstone reservoirs are insufficient for deep unconventional systems. Future research should prioritize integrated evaluation and protection methods tailored to deep tight, shale, and fractured–vuggy carbonate reservoirs. This review provides a basis for understanding complex damage mechanisms, developing functional protective materials, and advancing integrated reservoir protection technologies for the efficient development of deep unconventional resources. Full article

The vitreous body is not only a transparent filling material of the posterior segment; it is a soft, hydrated, and biologically active matrix that supports structural, optical, and biochemical homeostasis. Vitrectomy therefore leaves a functional deficit that current substitutes only partly address. Intraocular gases, silicone oils, and perfluorocarbon liquids remain essential surgical tools, but they mainly provide mechanical tamponade and do not reproduce native viscoelasticity, diffusion control, or protection against oxidative and inflammatory stress. This review considers vitreous replacement as a functional biomaterials challenge. We discuss native vitreous physiology, the limitations of present tamponade agents, and emerging bioengineered substitutes designed to create a more physiological intravitreal environment. Particular attention is given to hydrogel and polymer-based systems, especially hyaluronic acid-based and in situ crosslinked platforms, which are being developed to combine optical clarity, injectability, soft mechanical support, controlled degradation, and favorable tissue interaction. We also emphasize the need for standardized preclinical testing of swelling, enzymatic stability, drug diffusion, rheology, and long-term biocompatibility. Although next-generation materials may move the field beyond passive space filling, manufacturing reproducibility, regulatory validation, chronic safety, and cautious early-phase trials remain major translational barriers. Full article

Cellulose is the strongest cell wall polymer defining plant cell shape and growth, and the most abundant biopolymer on the Earth. Its synthesis by the plasma membrane (PM)-localized cellulose synthase complexes (CSCs) depends on surrounding lipids that establish the membrane microenvironment in which CSCs work and form vesicles delivering and removing CSCs to and from the PM by exo- and endocytosis. The role of exact lipid molecular species in these processes is poorly understood. In the present work we used hypocotyls of etiolated wild-type Col-0 and mutant ixr1-1 Arabidopsis thaliana seedlings grown with or without isoxaben, a specific cellulose synthesis inhibitor, as a model to reveal lipid molecular species associated with cellulose biosynthesis. Different lipid classes were separated by thin-layer chromatography (TLC) and their molecular species were analyzed by liquid chromatography–triple quadrupole tandem mass spectrometry (LC-QqQ-MS/MS). A total of 250 lipid molecular species were identified. Col-0 plants maintained stable levels of membrane glycerophospholipids but displayed significant remodeling of their acyl chains. In the presence of isoxaben, they accumulated three times more phosphatidic acids, a hallmark of a stress response. The isoxaben-resistant mutant ixr1-1 was characterized by a higher relative content of phosphatidylethanolamines, potentially rendering membranes more labile, as well as plastid galactolipids, which accumulated under isoxaben treatment. The multifaceted effects of isoxaben, including its impact on endomembrane lipids, suggest that it has additional binding sites beyond CSC. Full article

The valorization of lignocellulosic residues into bioactive and biodegradable materials offers a sustainable route for functional food packaging. In this study, hazelnut shells were exploited through an integrated process enabling the integrated recovery of polyphenols and cellulose. Polyphenols were extracted via hot water, liquid–liquid partitioning, and column chromatography, yielding a purified bioactive fraction. The residual biomass after polyphenol recovery was used for cellulose extraction (approximately 23% w/w) and converted into carboxymethyl cellulose (CMC) with a degree of substitution (DS) of 0.77. Active CMC films incorporating polyphenolic extracts exhibited improved mechanical performance, reaching tensile strengths of about 78 MPa and elongation at break values above 20%, while reducing water solubility to approximately 31%. The addition of carnauba wax further enhanced water resistance while modulating flexibility and stiffness. Attenuated Total Reflectance-Fourier Transform Infrared spectroscopy (ATR-FTIR) and scanning electron microscopy (SEM) analyses confirmed the conversion of crystalline cellulose into amorphous CMC and the successful incorporation of additives within the polymer matrix. The resulting films showed tunable mechanical, optical, and barrier properties, along with UV-blocking and antioxidant activity. These findings demonstrate that hazelnut shell-derived CMC films enriched with polyphenols and carnauba wax represent promising candidates for a sustainable platform for active food packaging applications, supporting a circular waste-to-value approach. Full article

Wastewater containing such inorganic contaminants, especially phosphate and nitrate ions, has to be treated thoroughly before disposal into natural environments. This is a precautionary measure to avoid adverse effects on public health, which are exacerbated when these two pollutants are present in an aqueous system. The present research investigated how the adsorption process is influenced by factors such as the effect of ion composition, contact time, temperature and competitive adsorption behavior in multi-anion systems using Ternary Biopolymer–Bentonite Beads. This study used five isotherms and four kinetic models to investigate phosphate ions removal on prepared natural Clay-Bio-polymer composite beads. The results indicate that the pseudo-second-order (PSO) kinetic model provides the most accurate description of the adsorption process. Moreover, the correlation coefficients (R²) obtained for both the Langmuir and Freundlich isotherm models are nearly equal to 1, confirming their strong reliability in fitting the experimental data. The strong fit of both the Langmuir and Freundlich models indicates that the adsorption process exhibits mixed behavior, with both monolayer adsorption on relatively homogeneous sites and multilayer adsorption on heterogeneous sites. This mixed-behavior system is typical of composite adsorbents with diverse surface properties. The Redlich-Peterson model, a hybrid of Langmuir and Freundlich, showed the best overall correlation (R² = 0.990 for H₂PO₄⁻ and 0.998 for NO₃⁻). The applicability of the Sips and Toth isotherm models, which account for both uniform and non-uniform adsorption behaviors, validated the experimental results. In the competitive binary system, the maximum adsorption capacities achieved by the composite were 121.844 mg/g for H₂PO₄⁻ and 27.979 mg/g for NO₃⁻. The results indicate strong competition between H₂PO₄⁻ and NO₃⁻ ions for the available active sites, reflecting an antagonistic adsorption. A positive value of ∆H° verifies that the adsorption process is endothermic and primarily physical, consistent with the experimental observations. The negative ∆G° values demonstrate that the adsorption occurs spontaneously, whereas the positive ∆S° indicates an increase in randomness at the solid–liquid interface during the uptake of phosphate ions. Full article

This article describes the development of a compact and affordable variable-temperature NMR instrument designed primarily to measure dynamic molecular motion in solids and liquids. The instrument consists of Lab-Tools’ Mk4 palm-top time-domain NMR spectrometer fitted with a Peltier-cooled variable-temperature probe inside a shimmed Halbach magnet. Measurement of NMR relaxation times T₁, T₂, and ${\mathrm{T}}_1\rho$ is possible over the temperature range −20 °C to 70 °C with cooling and heating rates, and data acquisition is controlled from an integrated mini-PC. The overall footprint of the instrument is roughly that of a shoe box, making both in-the-field and bench-top measurements possible. Applications of this instrument include measuring pore-size distribution in porous rocks, the viscosity of oils and tars trapped in porous rock, the properties of polymers, and the viscosity of the liquid components of foods (e.g. fruits, vegetables and seeds). Results of test measurements for calibrated oils and olive oil are presented together with measurements of molecular mobility in a solid polymer. Full article

Liquid electrolytes in conventional lithium-ion batteries pose safety risks associated with flammability, leakage, and explosion, whereas solid polymer electrolytes are generally limited by insufficient ionic conductivity at ambient temperature, restricting the development of high-energy lithium batteries. To address these issues, flexible poly (vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP)-based gel polymer electrolyte membranes (GPEs) were prepared via a slit-coating process combined with UV curing. NASICON-type lithium aluminum titanium phosphate (Li_1.3Al_0.3Ti_1.7P₃O₁₂, LATP) and garnet-type tantalum-doped lithium lanthanum zirconate (Li_6.4La₃Zr_1.4Ta_0.6O₁₂, LLZTO) were introduced as inorganic ceramic fillers to improve the ion-transport and interfacial properties of the GPE. Among the investigated samples, the PVDF-HFP-based GPE containing 10 wt% LLZTO exhibited the best overall performance, with an ionic conductivity of 3.40 × 10⁻⁴ S·cm⁻¹ at ambient temperature and a Li⁺ transference number of 0.77. Cyclic voltammetry results showed that the LLZTO-modified electrolyte membrane exhibited sharper and more symmetric redox peaks, higher peak current response, and better curve overlap during repeated cycles, indicating improved electrochemical reversibility and interfacial stability. In addition, LLZTO incorporation enhanced the mechanical strength, broadened the electrochemical stability window, and improved the flame-retardant behavior of the membrane. The LiFePO₄/GPE/Li cell assembled with the optimized membrane delivered an initial discharge capacity of 160 mAh·g⁻¹ at 0.1 C and maintained 80 mAh·g⁻¹ at 1 C, demonstrating good rate capability. Moreover, a capacity retention of 96% was maintained after 100 cycles at 0.1 C, confirming excellent cycling stability. Therefore, this work provides an effective strategy for the structural optimization and scalable preparation of high-performance gel polymer electrolyte membranes for lithium battery applications. Full article

Brewer’s spent grain (BSG), the main by-product of the brewing industry, is an abundant lignocellulosic residue that remains underused. In this study, antioxidant-rich extracts were obtained from BSG using pressurized liquid extraction (PLE) and subsequently incorporated into thermoplastic starch (TPS) films for sustainable food packaging applications. The phenolic profile analysis revealed 13 compounds, with caffeic acid and its hexoside as the most abundant. Extraction conditions were optimized using response surface methodology (RSM) to maximize yield and total phenolic content, showing that temperature had a significant positive effect. The selected extract had a total phenolic content of 3.19 mg/g dw and exhibited notable antioxidant activity. It was then incorporated into the polymer matrix, and the resulting films were analyzed for their structural, thermal, and antioxidant properties. The incorporation of BSG extracts improved the film antioxidant activity. Additionally, the release of phenolic compounds was evaluated and successfully described using a diffusion model based on Fick’s law, which allowed the calculation of a diffusion coefficient D = 2.63 × 10⁻⁸ cm²/s. Overall, the findings indicate that BSG-based extracts may represent promising functional additives for biodegradable polymer films, and the developed TPS films serve as proof-of-concept active packaging materials from renewable agro-industrial residues. Full article

DNA extraction is a critical prerequisite for reliable downstream analyses such as Polymerase Chain Reaction (PCR), sequencing, and genotyping. Conventional methods often require labor-intensive protocols, large sample volumes, or costly automation. Microfluidic approaches offer an alternative by reducing reagent consumption and enabling faster, more integrated workflows. Here, we present a passive lab-on-a-chip device that performs DNA extraction from complex biological media and enables subsequent on-chip single-molecule analysis. The chip integrates a magnetophoresis-based solid-phase extraction module with a fluorescence detection section capable of quantifying DNA molecules in microchannels and visualizing stretched molecules in nanochannels. The multi-level micro/nanofluidic architecture is fabricated in polymer using a single-step nanoimprinting process with a total manufacturing time of two minutes per chip, enabling scalable production. As a proof of concept, the device extracted DNA from samples spiked into buffer or plasma. On-chip transfer efficiency of DNA–bead complexes to the elution buffer reached 86%, and quantitative analysis of the recovered liquid showed an overall extraction efficiency of 40% (including DNA recovery off-chip), with intact 48 kbp DNA confirmed in both micro- and nanochannel measurements. This platform offers a promising foundation for point-of-care and point-of-interest applications, where integrated DNA extraction and analysis can reduce sample loss and support streamlined, automated workflows. Full article

Microneedles are a new technology in transdermal drug delivery that allows for the pain-free administration of drugs. Recently, these microneedles have gained popularity compared to traditional injections. Nevertheless, the selection of the most suitable materials is a significant issue, requiring a systematic analysis of various performance parameters. This paper developed a multi-criteria decision-making model based on the analytic hierarchy process (AHP) to systematically evaluate four primary material types for therapeutic microneedle applications: polymers, metals, ceramics, and silicon. The researchers defined five performance criteria, ranked by importance: biocompatibility (48.8%), mechanical properties (25.3%), manufacturability (15.8%), cost-effectiveness (6.6%), and compatibility with different types of microneedles (3.5%). The validity of the framework was established using the TOPSIS and ELECTRE methods, which showed strong agreement in the rankings, and a sensitivity analysis revealed that the rankings did not change with a ±20% variation in the parameters in 95% of the cases. The outcomes indicated that polymers are the most suitable, with the highest global priority score (38.3%), and they are good in biocompatibility (53.0% local priority), manufacturability (53.3%), and relative cost advantages (62.2%), though medical-grade polymer costs remain substantial. Metals were placed second (31.8%) due to their better mechanical properties (50.3%), followed by ceramics (17.6%) and silicon-based materials (12.3%). The framework offers clear decision guidelines: polymers for dissolving microneedle systems and controlled drug release applications; metals for precise liquid delivery devices; ceramics for specialized pharmaceutical uses that require extreme chemical compatibility; and silicon for research applications requiring precise geometries. Full article