Search Results (1,072)

Co-pyrolysis of polyolefins (LDPE, PP, PS) mixed with silicone rubber (SR) was investigated using a laboratory-scale pyrolysis apparatus to evaluate product composition, synergistic interactions, and siloxane recovery potential. Synergistic effects were assessed by comparing experimental mass balances and product distributions with calculated values derived from individual polymer pyrolysis. Co-pyrolysis resulted in a reduction in liquid yield and an increase in gaseous products and solid residue compared to calculated values, with liquid yields decreasing by up to ≈15 wt% at high SR content. This shift was accompanied by an enrichment in lighter hydrocarbons in both phases, reaching up to a ≈18% relative increase at high SR content, and by a redistribution towards smaller cyclic siloxanes. Chromatographic analysis confirmed that no new compounds were formed, but the proportion of low molecular weight species increased with silicone content. These effects are attributed to the distinct thermal behavior of the polymers, as silicone rubber does not melt but becomes brittle, allowing molten polyolefins to infiltrate surface cracks and prolong residence time, thereby promoting secondary cracking. Furthermore, recovery of hexamethylcyclotrisiloxane (D₃), the primary silicone pyrolysis product, was demonstrated from the liquid co-pyrolysis products via solvent-assisted filtration using ethanol, achieving purities above 99.5% and recovery rates up to ≈75% compared to other possible methods. These findings provide insights into co-pyrolysis behavior and offer a basis for developing strategies for the recovery of siloxane and advanced recycling of mixed polymer waste. Full article

Neopterin, a low-molecular-weight pteridine, is a biomarker of pro-inflammatory immune activity. Its levels rise in viral infections, transplant rejection, autoimmune, cardiovascular, and neurodegenerative diseases, and cancer. In healthy human serum, neopterin concentration values are up to 10 nM. Detection is challenging due to its low concentration and limited solubility. In this work, a sensitive and selective electrochemical sensor for neopterin was developed using polydopamine molecularly imprinted polymers on a glassy carbon electrode. The polymer films were electro-polymerized directly on the electrode, varying the ratio of polymer to neopterin, while non-imprinted films were prepared without the template for comparison. Rebinding and template removal were monitored by cyclic voltammetry using ferricyanide as a redox probe. All imprinted films exhibited a concentration-dependent response from 1.2 nM to 1.2 mM, with a rapid increase at low concentrations up to 120 nM and a slower approach to a plateau at higher concentrations. The highest response was observed in films with the greatest neopterin content, consistent with increased binding site availability. Full article

The release of CO₂ gas into the atmosphere is one of the most prolific causes of global climate change. To solve this problem, cost-effective technologies are being sought. Polymer membranes are innovative materials that can be widely used in the process of capturing and separating CO₂ gas. In this work, an amine impregnated and amidated solid sorbent (AISS) containing a copolymer (PMMA-co-AA), which consists of acrylic acid (AA) and methyl methacrylate (MMA), and PEPA (polyethylene polyamine), was synthesized. For the first time, sorbents based on homopolymers and copolymers of acrylic acid and methyl methacrylate were compared for their ability to capture CO₂ gas. Other than the synthesis of low swelling AISS, a calculation of its energy consumption, and a comparison of its cyclic capacity with 30% water solutions of monoethanolamine and methyldiethanolamine (MEA and MDEA) were performed. The solid sorbent PMMA-co-AAS showed a higher cyclic capacity than others, corresponding to the order PMMA-co-AAS (23 mg/g) > PAAS (16 mg/g) > MDEA (10 mg/g) > MEA (6 mg/g). The average absorption rate for these sorbents was in the sequence of MEA > PMMA-co-AAS > PAAS > MDEA at 40 °C, and the desorption rates were PMMA-co-AAS > PAAS > MDEA > MEA for these sorbents at 70 °C, correspondingly. When the amount of acrylic acid in the copolymer was varied from 0 to 100%, the copolymer’s water absorption capacity ranged from 0.2 to 1359.63%. Among them, the swelling ability of the chosen sorbent prepared from the 10% AA-containing copolymer and PEPA was 0.64%. Full article

The twin-blade planetary mixer is critical for processing highly viscous materials in the chemical and polymer industries, yet optimizing its mixing characteristics alongside energy efficiency remains challenging. This study investigates the twin-blade planetary mixer, using computational fluid dynamics simulation methods to analyze the operating parameters and multi-objective optimization of performance in viscous systems. First, the multi-axis stirring process was simulated numerically based on the Planetary Motion Method, revealing the working process at the cross-section and of the blades, thereby unveiling a mixing mechanism driven by cyclic transitions between local shear-intensive kneading and global convective circulation. Then, through orthogonal experiments and ANOVA, the dominant role of the hollow blade’s self-rotation speed on performance was clarified. Furthermore, based on Kriging and NSGA-II, with LINMAP employed for decision making, an optimal parameter combination, specifically a hollow blade self-rotation speed of 94.86 rpm, a speed ratio of 0.063, and a blade-to-bottom height of 2.79 mm, successfully achieved an 8.15% reduction in power consumption, a 20.03% increase in global axial flow, and a 5.01% enhancement in maximum kneading pressure. Full article

Molecularly imprinted polymers (MIPs) are widely employed for selective adsorption of target molecules in sensing and separation applications. The architecture of MIP films can influence adsorption behavior, interfacial stability, and reusability, yet systematic investigations of these effects are limited. This study aimed to evaluate how different polypyrrole (PPy) MIP film architectures affect the adsorption, stability, and regeneration characteristics of geraniol-imprinted layers on gold electrodes. Geraniol-imprinted and non-imprinted PPy films were electropolymerized onto quartz crystal microbalance (QCM) substrates. Two film architectures were compared: (i) a single-layer geraniol-imprinted PPy film, and (ii) a double-layer film consisting of a non-imprinted PPy underlayer followed by a geraniol-imprinted layer. Film characterization was performed using cyclic voltammetry (CV) and electrochemical quartz crystal microbalance (EQCM) measurements. Adsorption–desorption cycles were conducted to assess mass uptake, signal stability, and regeneration performance. EQCM analysis revealed that the double-layer architecture exhibited enhanced frequency signal stability during repeated adsorption–desorption cycles compared to single-layer films, suggesting a stabilizing effect of the underlying non-imprinted PPy layer at the electrode interface. Geraniol-imprinted films demonstrated significantly higher mass uptake than non-imprinted controls, confirming the sensitivity provided by molecular imprinting. Single-layer films showed more variability in signal response and less consistent regeneration performance. The architecture of MIP films significantly affects adsorption behavior, stability, and regeneration on electrode surfaces. Incorporating a non-imprinted PPy underlayer can improve signal reproducibility and enhance the robustness of MIP-based sensing interfaces. These findings provide guidance for the rational design of MIP coatings for electrochemical sensors and QCM-active platforms. Full article

In this work, we demonstrate a functional and previously insufficiently explored route for converting cyclic olefin copolymer (COC) TOPAS^® thin films into antibacterial hybrid materials through a combination of solvent casting, plasma activation, noble-metal sputtering, and subsequent thermal or laser treatment. While COC is already well-known as a transparent, chemically resistant material for pharmaceutical and optical applications, its coupling with post-treated noble-metal nanostructures for antibacterial functionality has not been systematically described. The main contribution of this study lies in showing that COC can serve not only as a passive packaging substrate, but also as an active platform for the formation of biologically relevant surface nanostructures. Compared with previously reported metal/polymer systems, the present work provides clear evidence that noble-metal layers on COC undergo substantial structural evolution after thermal and excimer-laser treatment, resulting in regular nanoclustered morphologies. A particularly important finding is the detection of Au particle implantation below the COC surface during sputtering, as revealed by Rutherford backscattering spectrometry, which distinguishes this system from conventional surface-only metal coatings. Furthermore, we show that laser and thermal processing do not merely reshape the deposited layer, but significantly influence the final biological response of the material. Ag-based structures showed strong bactericidal behavior against both Gram-negative Escherichia coli and Gram-positive Staphylococcus aureus. The prepared samples were comprehensively characterized by AFM, DSC, RBS, SEM, and TGA, and their roughness and wettability were also evaluated, enabling direct correlation between physicochemical changes and antibacterial performance. These results introduce a new strategy for upgrading conventionally used pharmaceutical COC materials into multifunctional surfaces with added antibacterial value. Full article

Flexible and biocompatible sensors are vital for a wide range of biomedical applications, including real-time health monitoring, intracranial pressure monitoring, knee replacement surgeries, wearables, and smart prosthetics. While various highly sensitive and stable pressure sensors have been demonstrated, they often lack the conformability and biocompatibility crucial for their wider application in various bio-integrated electronic systems. Herein, a piezoelectric pressure sensor is proposed using a hybrid polymer composite by leveraging the unique properties of Chitosan and Parylene C. Various material characterisations, such as XRD and FTIR, were performed to reveal structural and chemical characteristics of the novel composite material. Next, electromechanical characterisations of the pressure sensor were performed to reveal its dynamic sensing properties. The pressure sensor exhibits excellent sensitivity for both pressure and frequency, as well as cyclic stability (10³ cycles), wide pressure range (20–70 kPa), and biocompatibility. Full article

Candida albicans (C. albicans) is an opportunistic fungal pathogen and a major cause of nosocomial infections, especially in immunocompromised patients. Conventional diagnostic approaches such as blood culture and biochemical assays are accurate but require multi-step sample processing and prolonged turnaround times, limiting their applicability for rapid clinical screening. In the present study, we developed an electrochemical biosensor based on molecularly imprinted polymer (MIP) technology for the rapid and selective detection of intact C. albicans cells. The MIP layer was electropolymerized onto a screen-printed carbon electrode (SPCE), forming selective recognition cavities complementary to the fungal morphology. Electrochemical characterization and detection were performed using cyclic voltammetry in phosphate-buffered saline (PBS). The system demonstrated a wide linear detection range, enabling reliable quantification of C. albicans across concentrations spanning from 1 to 10⁴ CFU/mL and achieved an ultralow limit of detection (LOD) of 1.30 CFU/mL, demonstrating high sensitivity. High selectivity was confirmed against E. coli, S. aureus, and P. aeruginosa, demonstrating that the imprinted cavities effectively distinguish fungal cells from bacterial contaminants. These findings highlight the promise of MIP-based electrochemical biosensors as a simple, low-cost, and portable alternative for early fungal diagnostics. Full article

Polyether ether ketone (PEEK) is a high-performance polymer with exceptional mechanical properties, durability and lightweight. 3D printing of PEEK can be very beneficial in the medical industry to manufacture patient-specific implants; however, there is a lack of studies regarding the fatigue behavior of 3D-printed PEEK, especially under compression, which is closely related to its potential applications. This paper investigates the static and dynamic mechanical performance of 3D-printed PEEK. Tensile and compression tests were conducted on specimens with ±45° raster orientation. Annealing at 270 °C for 5 h increased crystallinity from 34.4% to 41.4% yet unexpectedly reduced tensile strength from 60.8 MPa to 47.3 MPa, while increasing Young’s modulus from 2.51 GPa to 3.51 GPa. Micro-CT analysis revealed increased pore size after annealing. Static compression strength showed improvement post-annealing, increasing from 80.1 MPa to 126.7 MPa, with modulus rising from 1.64 GPa to 2.28 GPa. Compression–compression fatigue tests, performed at 5 Hz and 2.5 Hz with stress amplitudes of 70–95% of maximum strength (R = 0.1), enabled the construction of the first S-N curve for 3D-printed PEEK under compressive loading. Annealed specimens exhibited superior fatigue life, with infinite life achieved at 83.3 MPa (70% of static strength). Thermal imaging highlighted the role of temperature in fatigue failure, showing that annealed specimens endured higher thermal loads. These findings support the suitability of 3D-printed PEEK for load-bearing biomedical applications under cyclic compressive loads. Full article

Haemophilus influenzae (H. influenzae) is an important respiratory pathogen that can cause various invasive and non-invasive bacterial infections requiring rapid and sensitive detection. In recent years, electrochemical biosensors have emerged as a practical alternative for pathogen detection due to their high sensitivity, portability and short analysis time. Molecularly imprinted polymers (MIPs) are a class of synthetic receptors designed to mimic biological recognition through template-directed polymerization. In this study, an electrochemical biosensor based on MIPs was developed for the selective detection of H. influenzae. The polymeric film composed of methacrylamide (MAM), acrylamide (AAM), and vinylpyrrolidone (VP) monomers was fabricated on a gold screen-printed electrode (gold-SPE). The results of cyclic voltammetry (CV) revealed a strong redox current shift corresponding to bacteria concentrations within an analytical range of 1–10,000 CFU/mL with LOD 1.03 CFU/mL, with relative standard deviation (RSD) values below 9% across the tested concentration range. The optimized composition yielded and exhibited excellent selectivity when tested against non-target bacteria such as Klebsiella pneumoniae, Pseudomonas aeruginosa, and Staphylococcus aureus. Full article

The paper presents results of a degradation analysis of polyamide 12 reinforced with carbon fibers used for additive manufacturing of cycloidal gear. Both FEM simulation and a fatigue test indicated the ability of the material to withstand loads during the work of cycloidal transmission. However, a run-to-failure (RTF) test revealed critical failure after 10⁵ cycles, with displacement and damage of the material in the area close to bearing instead of expected areas of teeth being in friction with pins. Acceleration analysis with time synchronous averaging (TSA) confirmed rapid degradation of the material’s strength at the end of the RTF test. It was found that the PA12 cycloidal gear damage was a result of fatigue accelerated by the temperature increase under the cyclic loads that took place during the RTF test. In particular, displacement of 0.2 mm did not appear in the specimens tested at 27 °C even after 10⁵ cycles, while at 140 °C this value was reached almost immediately. At 70 °C and 90 °C, plastic deformation of 0.2 mm was reached after 30,000 and 5000 cycles, respectively. The finding can be used in a predictive maintenance system of such cycloidal transmission with 3D-printed polymer gears. Full article

The reaction of the pyridylalcohol Ph₂C(OH)CH₂-2-py-6-Me (IH) with Me₃Al in refluxing toluene led to the isolation of the dimer [AlMe₂(μ-OC(Me)Ph₂)]₂ (1), whilst at ambient temperature the complex [(I)AlMe₂]·MeCN (2·MeCN) was isolated. Complex 1 is also readily available via the interaction of diphenylethanol and Me₃Al. Similar treatment of iPr₂C(OH)CH₂-2-py-6-Me (IIH) at ambient temperature afforded [(II)AlMe₂] (3). Treatment of IH and IIH with [VO(OiPr)₃] led to oxo-bridged complexes of the type [(VO)(μ₂-O)(I/II)]₂ (I (4·0.67MeCN), II (5)). The molecular structures of 1–5 are reported. These complexes have been employed as catalysts for the ring-opening polymerization (ROP) of the cyclic esters ε-caprolactone (ε-CL) and δ-valerolactone (δ-VL). For aluminium, complex 1/BnOH produced medium- to high-molecular-weight (M_n) PCL at 20 to 110 °C in solution, though some bi-/multi-modal behaviour was observed; for melts the M_n values were toward the lower end. For complexes 2 and 3, far lower M_n values for PCL were observed at 20 °C in solution and as melts, whilst in solution at 110 °C higher M_n values were achieved, though with less control. In general, M_n values for the PCL obtained using the vanadium complexes were low (≤8560 Da for 4, ≤2920 Da for 5). In the case of PVL, 1/BnOH in solution exhibited higher M_n values at lower temperatures with good control, and when employed as a melt, the M_n was toward the higher end (30,830 Da) observed. For 2/BnOH, much lower M_n values (≤2740 Da) were recorded both in solution and as a melt, whilst for 3, high M_n values were only observed in the absence of BnOH. Low M_n values (≤2920 Da) were also observed for the vanadium complexes 4 and 5. Kinetic results (both ε-CL and δ-VL) revealed that the vanadium complexes, particularly 4, outperformed the aluminium complexes. MALDI-ToF spectra revealed the formation of linear PCL polymers with BnO/H end groups for the aluminium/BnOH complexes in solution, and cyclic polymers when employed as melts. For vanadium, cyclic PCL polymers were the major family present. In the case of PVL, linear (BnO/H end groups) and cyclic polymers were observed when employing the Al/BnOH systems, whilst cyclic polymers were observed for vanadium. Copolymerization of ε-CL and δ-VL using 4/BnOH at 110 °C over 24 h led to incomplete conversion and formation of a random-type copolymer. Full article

Dental resin composites are routinely exposed to chemically aggressive beverages that may compromise long-term functional performance. This study investigated the structure–property–tribology relationships of four restorative composites (Filtek Z250, Filtek Z550, Herculite, and Herculite Ultra) subjected to cyclic immersion in beverages with different pH values. A total of 120 cylindrical specimens (7 mm diameter, 2 mm thickness; n = 5 per material per condition) were fabricated and exposed to mineral water, tea, coffee, Coca-Cola^®, Cola Light^®, and red wine for 28 days under cyclic conditions. Microhardness, surface roughness (Ra), steady-state coefficient of friction (COF), and mass variation were evaluated. All composites exhibited significant microhardness reduction after acidic exposure (p < 0.05), with the greatest decrease observed for Herculite Ultra in red wine (−47.4%) and Coca-Cola^® (−35.3%). Filtek Z250 demonstrated the highest baseline hardness and the lowest degradation susceptibility. Surface roughness changes were formulation-dependent, with Herculite Ultra showing pronounced roughening (ΔRa up to +0.074 µm), whereas Filtek Z550 exhibited erosion-driven smoothing (ΔRa down to −0.068 µm). Tribological behaviour was primarily governed by matrix softening rather than roughness alterations, with softened systems displaying unstable frictional responses (COF range: 0.127–0.697; p < 0.05). The results indicate that polymer matrix stability plays a more critical role in long-term functional performance than surface roughness or mass variation alone. Clinically, frequent exposure to acidic and solvent-containing beverages may accelerate mechanical and tribological degradation of susceptible composite formulations. Full article

This in vitro study assessed the impact of coconut milk, cow milk, and soybean oil on the surface roughness (Ra) of two milled (polymer-infiltrated ceramic network (PICN), Vita Enamic (EN) and resin nanoceramic (RNC), Cerasmart (CS)) and 3D-printed (VarseoSmile Crown plus (VS)) hybrid resin–ceramic materials. Standardized rectangular specimens were prepared and subjected to cyclic immersion in the test media at 37 °C for 30 days to simulate dietary exposure. Surface roughness was measured pre- and post-aging, and statistical analysis was performed using two-way ANOVA and paired t-tests (α = 0.05). All media significantly increased Ra across all materials (p < 0.001). While coconut milk and soybean oil caused comparable roughening (Ra up to 0.155 µm), cow milk exhibited a material-specific impact. It roughened milled materials (EN and CS) (Ra: 0.147–0.154 µm) significantly more than the 3D-printed material (VS) (Ra: 0.126 µm) (p < 0.05). Notably, all post-aging Ra values remained below the clinical bacterial adhesion threshold of 0.2 µm. In conclusion, while all tested dietary media significantly degraded the surface topography of hybrid resin–ceramics, the 3D-printed hybrid resin–ceramic material demonstrated superior resistance to cow milk compared to milled alternatives. Nonetheless, plaque retention risks remain clinically acceptable for all tested materials. Full article

In this work, poly(3-dodecylthiophene) (P3DDT) thin films were electrochemically synthesized onto fluorine-doped tin oxide (FTO) substrates via cyclic voltammetry using tetraethylammonium tetrafluoroborate (Et₄NBF₄) as the supporting electrolyte. Optical analyses were performed using ultraviolet–visible absorption spectroscopy (UV-Vis), photoluminescence spectroscopy (PL), emission ellipsometry (EE) and Raman spectroscopy. The results revealed the formation of distinct structures during the electropolymerization process, which significantly affected the optical behavior observed in the UV–Vis and PL spectra. Furthermore, the EE measurements provided insights into the impact of these structures on the polarization states of emitted and transmitted light on energy and charge transfer mechanisms and on the photophysical behavior of P3DDT. Variations in the degree of polarization (P), anisotropy factor (r), and asymmetry factor (g) were analyzed as a function of the emission wavelength. The results confirm the potential of P3DDT as an active layer in electroluminescent devices, as the emissive material used in the active layer consisted exclusively of this polymer. Full article