Search Results (962)

Proton spin–lattice and spin–spin NMR relaxation studies were conducted on lung tissue samples from 10 patients. For each case, relaxation properties of tumor tissue were compared with those of the corresponding reference tissue. The spin–lattice relaxation measurements were performed over a wide frequency range, from 10 kHz to 10 MHz, spanning three orders of magnitude. These were complemented by both spin–lattice and spin–spin relaxation data acquired at 18.7 MHz. Notably, the spin–spin relaxation process exhibited a bi-exponential character. This relaxation behavior was quantitatively analyzed using dedicated models to achieve two main goals: to evaluate the diagnostic potential of low-field NMR relaxometry, and to gain insights into the dynamics of water and macromolecules in tissue, in comparison with aqueous solutions of proteins and polymers. The frequency dependence of the spin–lattice relaxation rates was well described by a power-law function, with an exponent of approximately 0.3 closely matching the theoretical prediction for reptation dynamics in polymer systems, associated with the intermolecular relaxation contribution. The combined analysis of spin–lattice and spin–spin relaxation data revealed specific parameters (such as ratios between the relaxation rates or between the amplitudes of individual relaxation components) that can be considered as potential markers of pathological changes affecting molecular dynamics in tissues. Full article

The commercialization of rechargeable alkaline zinc–air batteries has been constrained by critical challenges associated with the zinc electrode, including passivation, dendrite growth, and hydrogen evolution reaction. These issues severely limit the cycle life and pose a major barrier to large-scale industrial deployment. Integration of porous anode structures and electrode additives—two widely investigated approaches for mitigating challenges related to zinc anode—shows significant promise. However, effectively combining these approaches remains challenging. This study introduces a method for fabricating zinc anodes that can combine the benefits of a porous structure and electrode additive. The polytetrafluoroethylene (PTFE) polymer binder used in fabricating the anode material resulted in a stable scaffold, providing the desired anode porosity of approximately 60% and effectively anchoring ZnO nanoparticles. The zinc anodes prepared using a nickel mesh current collector without any electrode additives demonstrated stable cycling performance, sustaining 350 cycles at a current density of 60 mA g_Zn⁻¹ with a coulombic efficiency of approximately 95%. Incorporating 2 wt.% Bi₂O₃ as an electrode additive further enhanced the cycling performance, achieving 200 stable cycles with 100% coulombic efficiency under an increased current density of 120 mA g_Zn⁻¹, signifying the effectiveness of the proposed fabrication strategy. Full article

A ceramic-based wideband capacitive-fed patch-loaded multi-layered rectangular dielectric resonator antenna (CFPL-ML-RDRA) with a compact form factor is proposed in this paper. The proposed antenna is composed of two ceramic substrates and a polymer as an adhesive. A capacitive-fed metallic patch structure is located on the top side of the bottom ceramic substrate. This novel structure generates two distinct resonant modes: the fundamental resonant mode of the RDRA and a hybrid resonant mode, which was confirmed through electric field (E-field) analysis and parametric studies. By merging these two resonant modes, the proposed antenna achieves a wide impedance bandwidth of 5.5 GHz, sufficient to cover the fifth-generation (5G) millimeter-wave (mmWave) frequency bands n257, n258, and n261 (5.25 GHz), while reducing the height of the DRA by 38.5% compared to the conventional probe-fed RDRA (PF-RDRA). Additionally, the 4 dBi realized gain bandwidth of the proposed CFPL-ML-RDRA is 5.4 GHz, which is 28.6% broader than that of the conventional PF-RDRA. To experimentally verify the antenna’s performance, the CFPL-ML-RDRA mounted on a test printed circuit board with a small ground size of 3.2 × 3.2 mm² was fabricated and characterized. The measured data align well with the simulated data. Furthermore, excellent antenna array performance was achieved based on array simulations. Therefore, the proposed antenna structure is well-suited for 5G mmWave mobile applications. Full article

Polymeric biocomposites are emerging as a new generation of eco-friendly and cost-effective materials that provide sustainable alternatives for the polymer industry while supporting environmental conservation. This study investigates the mechanical behavior of Low-Density Polyethylene (LDPE) compounds blended with natural rubber (NR) and reinforced with silanized Sugarcane Bagasse Ash (SCBA), chemically modified with bis(3 triethoxysilylpropyl) tetrasulfide (TESPT). Blends were formulated in LDPE/NR-SCBA weight ratios (wt%) of 90/10, 70/30, and 50/50, and processed at mixing speeds of 40 and 80 rpm to evaluate their potential as thermoplastic additives. Mechanical testing showed that blends mixed at 80 rpm achieved an 86% increase in elongation, while those processed at 40 rpm demonstrated a 78% enhancement in tensile strength. The incorporation of NR and vulcanizing systems markedly improved the overall mechanical properties of the composites. These biocomposites present promise for applications in the footwear industry (especially for soles) and for ergonomic molded components by conferring the advantageous combination of mechanical performance and esthetic appeal. Furthermore, development supports innovative manufacturing processes and contributes to reducing the industry`s carbon footprints, mitigating its negative impact on the planet. Full article

High-performance batteries for military and extreme environment applications require alternatives to conventional liquid lithium-ion batteries (LIBs), which suffer from poor low-temperature performance and safety risks. All-solid-state lithium batteries (ASSLBs) offer enhanced safety and superior low-temperature capability. In this work, we designed and fabricated composite solid-state electrolytes using polyvinylidene fluoride (PVDF) and polyacrylic acid (PAA) as polymer matrices, N,N-dimethylformamide (DMF) as the solvent, and lithium bis(trifluoromethane sulfonimide) (LiTFSI) as the lithium salt. Composite solutions with varying PAA mass ratios were prepared. Advanced three-dimensional (3D) printing technology enabled the rapid and precise fabrication of electrolyte membranes. An ionic conductivity of about 2.71 × 10⁻⁴ S cm⁻¹ at 25 °C, high mechanical strength, and good thermal properties can be achieved through component and 3D printing process optimization. Assembled LiCoO₂||PVDF@PAA||Li ASSLBs delivered an initial discharge capacity of 165.3 mAh/g at 0.1 mA cm⁻² (room temperature), maintaining 98% capacity retention after 300 cycles. At 0 °C, these cells provided 157.4 mAh/g initial capacity with 85% retention over 100 cycles at 0.1 mA cm⁻². This work identifies the optimal PAA ratio for enhanced electrochemical performance and demonstrates the viability of 3D printing for advanced ASSLB manufacturing. Full article

Waste drilling fluids represent a complex gel–colloidal system containing structurally stable polymeric networks and heavy-metal ions that can cause tremendous damage to the ecosystem. The current disposal methods, like solidification/landfills, formation reinjection, and chemical treatment, commonly suffer from high secondary pollution risks, poor resource recovery, and incomplete detoxification. This paper developed a photocatalytic approach to complex gel system treatment by hydrothermally synthesizing a novel sulfur-doped, oxygen-vacancy-modified 3D flower-like xS-BiOBr_0.5Cl_0.5 structure which effectively narrowed the bandgap of BiOX and thus significantly enhanced its catalytic activity. The chemical composition, morphology, specific surface areas, and bandgaps of the materials were characterized. The photocatalytic performance and cyclic stability of the materials were measured, and 0.5S-BiOBr_0.5Cl_0.5 showed the best photocatalytic performance. The rhodamine B(RhB) degradation and polymer degradation efficiencies of 0.5S-BiOBr_0.5Cl_0.5 were up to 91% and 79%, respectively, while the Hg(II), Cr(VI), and Cr(III) reduction efficiencies of the material were up to 48.10%, 96.58%, and 96.41%, respectively. The photocatalytic mechanism of the xS-BiOBr_0.5Cl_0.5 materials was evaluated through an oxygen vacancy analysis, active species capture experiments, and density functional theory (DFT) computations. Overall, the xS-BiOBr_0.5Cl_0.5 materials can provide a low-cost and harmless treatment method for waste drilling fluids and promote the “green” development of oil and gas. Full article

Plastic pollution in freshwater ecosystems is an increasing environmental concern, prompting the search for biodegradable polymer (BP) alternatives. However, their degradation in natural aquatic environments remains poorly investigated and understood. This four-month in situ study compared the degradation in a lentic freshwater ecosystem of two compostable items, Mater-Bi^® shopping bag and disposable dish, with their respective pure polymer matrices, poly(butylene adipate-co-terephthalate) (PBAT) and polylactic acid (PLA). Additionally, biodegradable poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) and oil-based polypropylene (PP) were also tested. Changes in morphology, chemical composition and thermal and mechanical properties, as well as microbial colonization, were analyzed over time. A validated cleaning protocol was employed to ensure accurate surface analysis. Results showed detectable but limited degradation of pure polymers and their matrices in commercial products after 120 days of immersion with variations observed among polymer materials. Compostable materials exhibited significant leaching of fillers (starch, inorganic particles), leading to morphological changes and fragmentation. PHBV showed the fastest degradation among tested polyesters. PP exhibited only minor surface changes. Microbial colonization varied with polymer structure and degradability, but long-term degradation was limited by polymer properties and the gradual development of the plastisphere. This study highlights that standard laboratory tests may overestimate the environmental degradability of BPs and emphasizes the importance of in situ assessments, careful cleaning procedures and property characterizations to accurately assess polymer degradation in freshwater systems. Full article

This work analyzes the radiation shielding effectiveness of biocompatible hydrogel pads containing carbohydrate-based polymer matrices (Alginate, Chitosan, and Cellulose) integrated with the high atomic number (Z) fillers Bismuth Oxide (Bi₂O₃) and Zinc Oxide (ZnO). The Monte Carlo-based toolkit, Geant4, was used to simulate the deposition of the dose throughout a multilayer phantom that mimics the skin (Epidermis, Dermis, Subcutaneous, and Muscle) with a pad on top irradiated with photon and electron beams from 50 keV to 1000 keV. The results indicated that Bi₂O₃ succeeded in causing greater absorption of photons at doses, particularly in deep-layer tissues, from the increase in the filler content as well as the pad thickness. The Cellulose–Bi₂O₃ composites (10 mm thick) not only showed the best deep-shielding property among all investigated combinations but also the Alginate-based pads generally performed better with regard to the surface dose attenuation. The results demonstrate the promising potential of high-Z-doped hydrogels in serving as flexible, light, and biocompatible shielding materials for superficial radiotherapy. Full article

In the field of advanced electrical energy conversion and storage, remarkable attention has been given to the development of new, more sustainable electrolytes. In this regard, the combination of redox shuttles with aqueous bio-polymer gels seems to be a valid alternative via which to overcome the typical drawbacks of common liquid electrolytes such as corrosion, volatility or leakage. Despite the promising results obtained so far, redox-active species such as bis(6,6′-dimethyl-2,2′-bipyridine)copper(I) trifluoromethanesulfonylimide, ([Cu(I)(dmby)₂]TFSI), still present inherent challenges associated with their poor water solubility and oxidative lability, which prevents their employment in cheap and sustainable aqueous electrolytes. The present study investigates the stabilization of the Cu(I) complex ([Cu(I)(dmby)₂]TFSI) within two natural hydrogels based on the biopolymers κ-carrageenan and galactomannan, using ZnO nanoparticles as gelling agents. These eco-friendly and biocompatible systems are proposed as potential matrices for quasi-solid electrolytes (QSEs), offering a promising platform for advanced electrolyte design in electrochemical applications. Both hydrogels effectively stabilized and retained the redox species within their networks. In order to shed light on distinct stabilization mechanisms, complementary FTIR and SEM analyses were relevant to reveal the structural rearrangements, specific to each matrix, upon complex incorporation. Furthermore, thermogravimetric analysis confirmed notable thermal resilience in both systems, with the galactomannan-based gel demonstrating enhanced performance. Altogether, this work introduces a novel strategy for embedding copper-based redox couples into gelled electrolytes, paving the way toward their integration in real electrochemical devices, where long-term stability, redox retention, and energy conversion efficiency are critical evaluation criteria. Full article

Polyethylene terephthalate (PET) is a widely used polymer whose accumulation in the environment poses a significant pollution challenge. This study explores the degradation of bis(2-hydroxyethyl) terephthalate (BHET) and terephthalic acid (TPA)—two monomers commonly produced during PET hydrolysis and widely used as intermediates in PET recycling—through Advanced Oxidation Processes (AOPs) employing KrCl (222 nm) and XeBr (283 nm) excimer lamps in the presence of hydrogen peroxide (H₂O₂). The effects of the H₂O₂/monomer mass ratio, initial monomer concentrations, and reaction volume on degradation efficiency were systematically evaluated. The results demonstrate that excimer lamp technology, particularly KrCl, holds promising potential for the effective degradation of both BHET and TPA, and thus represents a viable strategy for PET waste treatment. Full article

Transparent polyimides with excellent mechanical properties and high optical transmittance have been widely used in various optical and electrical applications. However, due to the rigidity of their aromatic structure, their flexibility is limited, making them unsuitable for applications requiring different form factors, such as flexible display cover windows. Furthermore, the refractive index of most transparent polyimides is approximately 1.57, which differs from that of the optically clear adhesives (OCAs) and window materials that have values typically around 1.5, resulting in visual distortion. This study employed 4,4′-(hexafluoroisopropylidene)diphthalic anhydride (6FDA) and 2,2′-bis(trifluoromethyl)benzidine (TFMB) as the base structure of polyimides (6T). Additionally, 1,3-bis(aminomethyl)cyclohexane (BAC) with a monocyclic structure and bis(aminomethyl)bicyclo[2,2,1]heptane (BBH) with a bicyclic structure were introduced as co-monomers or crosslinking agents to 6T. The mechanical, thermal, and optical properties of the obtained copolymers (6T-BAC and 6T-BBH series) and crosslinked polymers (6T-CL-BAC and 6T-CL-BBH series) were compared. Both the copolymer series (6T-BAC and 6T-BBH) and the crosslinked series (6T-CL-BAC and 6T-CL-BBH) exhibited improved optical properties compared to the conventional 6T, with maximum transmittance exceeding 90% and refractive indices ranging from approximately 1.53 to 1.55. Notably, the copolymer series achieved transmittance levels above 95% and exhibited lower refractive indices (~1.53), demonstrating superior optical performance relative not only to the 6T baseline but also to the crosslinked series. The alicyclic polyimides synthesized in this study exhibited mechanical flexibility, high optical transmittance, and a refractive index approaching 1.5, demonstrating their applicability for use as flexible display cover window materials. Full article

Proton therapy has emerged as a highly precise and tissue-sparing radiotherapy technique, capitalizing on the unique energy deposition pattern of protons characterized by the Bragg peak. Ensuring treatment accuracy relies on calibration phantoms, often composed of tissue-equivalent polymeric materials. This study investigates the dosimetric behavior of four commonly used polymers—Parylene, Epoxy, Lexan, and Mylar—by analyzing their linear energy transfer (LET) values and Bragg curve characteristics across various proton energies. Experimental LET data were collected and used to train and evaluate the predictive power for Bragg peak of multiple artificial intelligence models, including kNN, SVR, MLP, RF, LWRF, XGBoost, 1D-CNN, LSTM, and BiLSTM. These algorithms were optimized using 10-fold cross-validation and assessed through statistical error and performance metrics including MAE, RAE, RMSE, RRSE, CC, and R². Results demonstrate that certain AI models, particularly RF and LWRF, accurately (in terms of all evaluation metrics) predict Bragg peaks in Epoxy polymers, reducing the reliance on costly and time-consuming simulations. In terms of CC and R² metrics, the LWRF model demonstrated superior performance, achieving scores of 0.9969 and 0.9938, respectively. However, when evaluated against MAE, RMSE, RAE, and RRSE metrics, the RF model emerged as the top performer, yielding values of 12.3161, 15.8223, 10.3536, and 11.4389, in the same order. Additionally, the SVR model achieved the highest number of statistically significant differences when compared pairwise with the other eight models, showing significance against six of them. The findings support the use of AI as a robust tool for designing reliable calibration phantoms and optimizing proton therapy planning. This integrative approach enhances the synergy between materials science, medical physics, and data-driven modeling in advanced radiotherapy systems. Full article

In this work, bio-based thermoelectric composites were developed using acrylated epoxidized soybean oil (AESO) as the polymer matrix and bismuth telluride (Bi₂Te₃) as the thermoelectric filler. The materials were formulated for both UV-curing and thermal-curing processes, with a focus on Digital Light Processing (DLP) 3D printing. Although UV curing proved ineffective at high filler concentrations due to the light opacity of Bi₂Te₃, thermal curing enabled the fabrication of stable, homogeneously dispersed composites. The samples were thoroughly characterized through rheology, FTIR, TGA, XRD, SEM, and density measurements. Thermoelectric performance was assessed under a 70 °C temperature gradient, with Seebeck coefficients reaching up to 51 µV/K. Accelerated chemical degradation studies in basic media confirmed the degradability of the matrix. The results demonstrate the feasibility of combining additive manufacturing with sustainable materials for low-power thermoelectric energy harvesting applications. Full article

The development of a silane coupling agent with an aminopropyl structure as a nucleating agent for poly(ethylene terephthalate) (PET) is reported in this study. The tri–block oligomers nucleating agent was formed by 1,3-bis(3-aminopropyl)-1,1,3,3-tetramethyldisiloxane/oxalic acid/low molecular weight PET (LPOBD). It was subsequently cross-linked with tetraethyl orthosilicate to form LPOBD-T. Composites of LPOBD/PET and LPOBD-T/PET were prepared by melt blending, and their thermal and crystallization behaviors were analyzed using XRD, DSC, TG, and POM. The results indicated that not only did the triblock polymer nucleating agent LPOBD exhibit a strong nucleation effect, but the crosslinked LPOBD-T also demonstrated superior crystallization performance. Specifically, the crystallinity of the 1 wt% LPOBD-T/PET composite increased by 3.3%, the crystallization temperature rose by 21.1 °C, and the t_1/2 was reduced by 53 s. Moreover, the crystalline morphology was more uniform. These findings indicate that the tri-block oligomers synthesized from a silane coupling agent serve as effective nucleating agents for PET. Full article

A new approach in amperometric enzyme electrodes production based on all-electrochemically assisted procedures will be described. Enzyme (glucose oxidase) immobilization was performed by in situ co-crosslinking of enzyme molecules through electrophoretic protein deposition, assuring enzyme immobilization exclusively onto the transducer surface (Pt electrode). Analogously, the poor selectivity of the transducer was dramatically improved by the electrosynthesis of non-conducting polymers with built-in permselectivity, permitting the formation of a thin permselective film onto the transducer surface, able to reject common interferents usually found in real samples. Since both approaches required a proper and distinct electrochemical perturbation (a pulsed current sequence for electrophoretic protein deposition and cyclic voltammetry for the electrosynthesis of non-conducting polymers), an appropriate coupling of the two all-electrochemical approaches was assured by a thorough study of the likely combinations of the electrosynthesis of permselective polymers with enzyme immobilization by electrophoretic protein deposition and by the use of several electrosynthesized polymers. For each investigated combination and for each polymer, the analytical performances and the rejection capabilities of the resulting biosensor were acquired so to gain information about their sensing abilities eventually in real sample analysis. This study shows that the proper coupling of the two all-electrochemical approaches and the appropriate choice of the electrosynthesized, permselective polymer permits the easy fabrication of novel glucose oxidase biosensors with good analytical performance and low bias in glucose measurement from typical interferent in serum. This novel approach, resembling classical electroplating procedures, is expected to allow all the advantages expected from such procedures like an easy preparation biosensor, a bi-dimensional control of enzyme immobilization and thickness, interferent- and fouling-free transduction of the electrodic sensor and, last but not the least, possibility of miniaturization of the biosensing device. Full article