Polyvinylpyrrolidone Research Articles

Tumor Microenvironment Reprogrammed Bimetallic Hybrid Nanostimulator for Triggering Radio-Cuproptosis-Immunotherapy.

Radio-immunotherapy driven by radiation-induced immunogenic cell death (ICD) is emerging as a potential opportunity to address conventional radiotherapy (RT) that is only applicable to localized tumor treatment. However, the effective activation of ICD during RT is severely limited by radiation dose, weak tumor immunogenicity, and radio-resistance caused by tumor microenvironment (TME). Herein, a novel bimetallic hybrid nanoscale coordination nanostimulator is first proposed by phosphate backbone doped with copper ions (Cu2+) and hafnium ions (Hf4+), and then modified with polyvinylpyrrolidone (PVP). The PVPylated Cu/Hf-doped phosphate nanostimulator (denoted as CHP) exhibits effective reprogramming of TME, including depletion of tumor endogenous glutathione (GSH), relief of tumor hypoxia and repolarization of M2 phenotypic macrophages, thus achieving tumor radiosensitization at low X-ray irradiation dose, gradually accumulation of tumor endogenous reactive oxygen species (ROS) and augmenting cuproptosis. In addition, cuproptosis can amplify RT-induced anti-tumor immunity through ICD activation, ultimately resulting in a robust anti-tumor immune response and long-term immunity, evidenced by distant tumor growth inhibition of 4T1-tumor-bearing models. More interestingly, it is discovered that CHP-mediated cuproptosis can be intensifiable during X-ray irradiation. Taken together, this work presents a novel radio-cuproptosis-immunotherapy cascade strategy, offering a new perspective for innovation in the treatment field of breast cancer.

Comprehensive study on dielectric properties and proton conductivity of graphene oxide (GO) embedded PVdF/PVP membrane electrolytes

This article investigates how the presence of polyvinylpyrrolidone (PVP) affects the dielectric properties and proton conductivity of phosphoric acid (PA) doped PVdF/PVP-based composite polymer electrolytes supported by graphene oxide (GO). In the study, insights into the structural, morphological, and thermal characteristics of the proposed composite electrolytes are obtained using characterization techniques such as Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), and thermogravimetric analysis (TGA). Proton conductivity and dielectric measurements are carried out across a frequency and temperature range (20 Hz-1 MHz, 300–420 K). We conduct in-depth discussions on the dielectric properties, including AC conductivity (σac), dielectric permittivity (ε′), imaginary permittivity (ε″), and loss tangent (tanδ) of the polymer electrolytes. While GO enhances the thermomechanical properties, the highest proton conductivity values are observed for (PVdF70/PVP30)-GO and (PVdF50/PVP50)-GO electrolytes, reaching 4.4 × 10−5 and 6.1 × 10−4 S/cm respectively. The dielectric measurements revealed a significant increase in the dielectric constant (ε′) and dielectric loss (ε″) values for the composite membranes, especially at lower frequencies and higher temperatures. For instance, the (PVdF50/PVP50)-GO composite exhibited ε′ values of 8.8 × 106, 1.99 × 105, and 77.38 at frequencies of 20 Hz, 1 kHz, and 1 MHz, respectively, at 300 K, and 7.38 × 106, 2.76 × 104, and 430.5 at 420 K. The ε″ values at 300 K for the same composite were 16.18 × 106, 7.25 × 105, and 1.09 × 103, respectively, at the same frequencies. (PVdF50-PVP50)-GO exhibits the lowest relaxation time (τ) and the highest proton conductivity at ambient temperature. These findings underscore the intricate interplay between PVP content, dielectric properties, and proton conductivity, providing valuable insights for the advancement of polymer electrolyte materials. This study contributes to our understanding of PA-doped (PVdFx/PVPy)-GO electrolytes, with implications for electronic and energy storage devices.

Ferrous ascorbate non-effervescent floating mini-caplets as an oral iron supplement.

This research aimed to develop non-effervescent floating mini-caplets of Ferrous Ascorbate (FA) using low-density polymers to overcome the problems of poor bioavailability associated with immediate-release iron products.Methods:The excipients and method (melt granulation) were selected based on pre-and post-compression parameters in trial batches. The formulation was optimized by a full factorial 32 experimental design. An optimized formulation was evaluated for drug release kinetic, accelerated stability study, and in vivo study in healthy adult New Zealand female rabbits.Results:The optimized formulation F6 mini-caplets (42.5% FA, 45% Glyceryl palmitostearate asPrecirol, 10% polyvinyl pyrrolidone K-30, and 2.5% lactose) were found to have instant floating and 12h floating duration in 0.1N Hydrochloric acid (HCl) dissolution medium. In vitro drug release (diffusion mechanism) at 1h and 5h was 30-35% and 65-70%, respectively. It was found stable for three months under an accelerated stability study. In vivo study showed significantly increased serum iron levels and decreased unsaturated iron binding capacity (UIBC) in the test group (optimized formulation) compared to control and standard (immediate-release iron).Conclusion:Based on the in vitro and in vivo results, we conclude that non-effervescent floating FA mini-caplets have higher bioavailability compared to immediate release FA, which may be attributed to prolonged iron release at its absorption site due to their retention in the gastric region. Hence, non-effervescent floating FA mini-caplets may act as a potential approach for iron deficiency.

FORMULATION OF PROPOLIS-BASED RECURRENT APHTHOUS STOMATITIS (RAS) PROTECTIVE PATCH WITH COMBINATION OF PVP AND CELLULOSE MATERIALS

Objective: The objective of this study was to obtain a mucoadhesive patch for recurrent aphthous stomatitis (RAS) with propolis, proven propolis’ antibacterial ability against bacteria in the oral cavity, and to obtain the physical characteristics of the produced patch. Methods: The patch was produced using a solvent-casting method. The antibacterial properties were determined by the disc diffusion method against S. mutans, S. oralis, S. sanguinis, and S. gingivalis. The physical characteristics of the patch was determined by examining weight and thickness dimension, swelling, surface pH, and structure observation. Results: The patch was made from 8 formulations with different propolis concentrations, Polyvinylpyrrolidone (PVP), and the use of cellulose materials (Hydroxypropyl methylcellulose and Carboxymethylcellulose). The concentrations of propolis used were 3%, 5%, 7%, and 10%. While the ratio of PVP and cellulose material in the formulation is 2:1. Results showed that propolis had a zone of inhibition greater than 2 mm against S. oralis, S. sanguinis, S. mutans, and P. gingivalis bacteria. Patches produced were clear to brown-colored films with high swelling percentage due to hydrophilic polymers used. The patch thickness that is closest to the requirements of the buccal patch was F8 with 0.36+0.04 mm. The mean values of the patches have matched normal salivary pH of 5.5–7. Physically, PVP/CMC formulations were more sticky, and the PVP/HPMC patches were more solid and stronger. Conclusion: A mucoadhesive patch was obtained with a combination of PVP/CMC and PVP/HPMC, tween 80 as a surfactant, glycerin as a plasticizer, peppermint oil as a flavor enhancer and preservative, with the active ingredient propolis.

Meso-Macroporous Hydroxyapatite Powders Synthesized in Polyvinyl Alcohol or Polyvinylpyrrolidone Media.

Mesoporous hydroxyapatite (HA) is widely used in various applications, such as the biomedical field, as a catalytic, as a sensor, and many others. The aim of this work was to obtain HA powders by means of chemical precipitation in a medium containing a polymer-polyvinyl alcohol or polyvinylpyrrolidone (PVP)-with concentrations ranging from 0 to 10%. The HA powders were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, atomic emission spectroscopy with inductively coupled plasma, electron paramagnetic resonance, scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The specific surface area (SSA), pore volume, and pore size distributions were determined by low-temperature nitrogen adsorption measurements, and the zeta potential was established. The formation of macropores in powder agglomerates was determined using SEM and TEM. The synthesis in 10% PVP increased the SSA from 101.3 to 158.0 m2/g, while the ripening for 7 days led to an increase from 112.3 to 195.8 m2/g, with the total pore volume rising from 0.37 to 0.71 cm3/g. These materials could be classified as meso-macroporous HA. Such materials can serve as the basis for various applications requiring improved textural properties and may lay the foundation for the creation of bulk 3D materials using a technique that allows for the preservation of their unique pore structure.

A scalable and universal strategy for constructing long-term antibacterial coatings with lubricant property on medical catheters

Medical catheters might cause a high morbidity of catheter-associated urinary tract infections (CAUTIs) because of the bacterial adhesion onto the surface. In addition, the inherent hydrophobicity of catheter materials exacerbates mechanical friction, leading to tissue damage. Therefore, coatings with integrated antibacterial and lubricative properties are appealing approaches to mitigate these challenges. In this study, a kind of polyurethane (PU)-based coatings were developed and prepared on medical catheters, which were modified with a cationic antibacterial agent, quaternized ammonium-modified methyldiethanolamines (QMDEAs). Due to the reaction among castor oil tertiary alcohols, isocyanates and QMDEAs, a polymer cross-linked network was fabricated, in which a hydrophilic polymer, polyvinylpyrrolidone (PVP), was added to form a semi-interpenetrating network. The structures of the coatings were regulated by adjusting the lengths of alkyl chain of QMDEAs, concentrations of pre-coated solutions, ratios of QMDEA:isocyanate, and parameters of preparation process. Among the coatings we prepared, PU-C10–46 possessed the optimized performances, which reduced the dynamic friction coefficient by 91.38 % and had the antibacterial efficiency of 99.9 % with good biocompatibility. The in vivo anti-infective properties of PU-C10–46 were also demonstrated by an infected animal model. Furthermore, PU-C10–46 was produced in an industrial equipment, and the large-scaled industrial products also had the same performances. This work could provide a promising strategy to deal with the challenges of medical catheter-associated infection.

Contrasting the pharmacokinetic performance and gut microbiota effects of an amorphous solid dispersion and lipid nanoemulsion for a poorly water-soluble anti-psychotic

Increasing attention is being afforded to understanding the bidirectional relationship that exists between oral drugs and the gut microbiota. Often overlooked, however, is the impact that pharmaceutical excipients exert on the gut microbiota. Subsequently, in this study, we contrasted the pharmacokinetic performance and gut microbiota interactions between two commonly employed formulations for poorly soluble compounds, namely 1) an amorphous solid dispersion (ASD) stabilised by poly(vinyl pyrrolidone) K-30, and 2) a lipid nanoemulsion (LNE) comprised of medium chain glycerides and lecithin. The poorly soluble antipsychotic, lurasidone, was formulated with ASD and LNE due to its rate-limiting dissolution, poor oral bioavailability, and significant food effect. Both the ASD and LNE were shown to facilitate lurasidone supersaturation within in vitro dissolution studies simulating the gastrointestinal environment. This translated into profound improvements in oral pharmacokinetics in rats, with the ASD and LNE exerting comparable ∼ 2.5-fold improvements in lurasidone bioavailability, compared to the pure drug. The oral formulations imparted contrasting effects on the gut microbiota, with the LNE depleting the richness and abundance of the microbial ecosystem, as evidenced through reductions in alpha diversity (Chao1 index) and operational taxonomical units (OTUs). In contrast, the ASD exerted a ‘gut neutral’ effect, whereby a mild enrichment of alpha diversity and OTUs was observed. Importantly, this suggests that ASDs are effective solubility-enhancing formulations that can be used without comprising the integrity of the gut microbiota – an integral consideration in the treatment of mental health disorders, such as schizophrenia, due to the role of the gut microbiota in regulating mood and cognition.

Synthesis of Nixp/C Nanofibers As Interlayer and Sulfur Host for Lithium-Sulfur Batteries

Lithium-sulfur batteries (LSB) have a high theoretical capacity (1675 mAh g − 1) and energy density (2600 Wh kg−1), making them one of the most promising energy storage systems. 1 However, it has some limitations, such as “shuttle effect” of polysulfides and high volume expansion, causing poor cycle performance of the battery.The transition metal phosphides with carbon materials as sulfur host for LSB have attracted extensive scientific focus due to the large surface area and strong chemisorption ability. Moreover, high electrical conductivity of carbon-based material and the chemical adsorption effect of Ni-P phase can reduce the “shuttle effect”, and improve the cyclability of the material. 2,3 In this work, nickel phosphide carbon composite (NixP/C) nanofibers were synthesized using a water-soluble carbon source polyvinylpyrrolidone (PVP) and cost-effective electrospinning method. The impact of humidity on the physical and electrochemical characteristics of the electrospun NixP/C nanofibers was studied, utilizing them as interlayer and sulfur host material for LSB.The NixP/C nanofibers were synthesized using an electrospinning machine from PVP, nickel nitrate hexahydrate, and phosphoric acid as precursors. The nanofibers were electrospun at 18 kV voltage and 0.8 mL h–1 flow rate. The electrospinning humidity (RH) varied between 19-35%. Obtained nanofibers were dried at 110 ºC for 11 h. Finally, prepared fibers were annealed at 700 ºC for 1 h with a heating rate of 5 ºC min-1 in the N2 + H2 (4%) atmosphere.The crystalline phases of the final products were observed using X-Ray diffraction (XRD, Miniflex, Rigaku). The microstructure was studied by transmission electron microscopy (TEM, JEM-1400 Plus, JEOL). According to the results shown in Figure 1, Ni2P with a hexagonal structure and the space group of P62m, and Ni12P5 with a tetragonal structure, space group of 87:I4/m were formed. Nanoparticles of NixP are uniformly distributed within the carbon fiber matrix (inset).The NixP/C freestanding mats were embedded as a sulfur host or interlayer for LSB in CR2032 coin-type cells. 1 M Li2S6 catholyte solution and 1 M LiTFSI in 1,3- dioxolane (DOL)/1,2 dimethoxyethane (DME) (v/v, 1:1) with 2 wt% of LiNO3 were used as a source of sulfur and electrolyte, respectively. Further details and obtained results will be presented at the conference. Acknowledgements This research was funded by the projects AP13068219 “Development of multifunctional free-standing carbon composite nanofiber mats”, and AP19675260 “Development of nanofibrous electrode materials for next-generation lithium-ion batteries” from the Ministry of Education and Science of the Republic of Kazakhstan.

Printable MXene Ink Hybridized with ZSM-5 for Gas Sensing and CO2 Capturing

In this work we present preparation, characterization and microprinting of Ti3C2/ZSM-5 ink. Printable inks with a viscosity of 5-6 cP were prepared by ultrasonic dispersion of Ti3C2/ZSM-5 nanopowders in DMSO solvent using 1% Polyvinylpyrrolidone (PVP) as dispersant. Brunauer Emmett Teller (BET) results indicate a type IV adsorption isothermal curve for N2 gas with a type H4 retention ring. The data show that the average pore size of the composite material is 23nm, indicating that the material has a micro-mesoporous structure and exhibits excellent adsorption properties for gas sensing applications. However, the adsorption and desorption curves of CO2 shows hysteresis indicating strong interaction between functional groups on the material and CO2 molecules. This material has high CO2 adsorption performance and desorption hysteresis effect, indicating that it can be directly used for CO2 capture. Thermogravimetric (TGA) analysis showed the thermal stability of the composite, with a mass loss of only 5% at 800℃. Ti3C2/ZSM-5 composite ink has excellent anti-oxidation and dispersion properties. When the pure MXene interlayer void is exposed to air, the Ti element in MXene is easily oxidized to TiO2. The introduction of ZSM-5 not only limits the interaction between the functional groups on the surface of MXene, but also fills the layer gap of MXene, effectively reduces the contact with oxygen, and thus shows good oxidation resistance. No characteristic valence signal of TiO2 was observed in XPS results, which confirmed the effectiveness of the method. In addition, imidazole acid molecular sieve frame strengthened MXene adsorption, will have broad prospect of application in gas sensing field. In traditional printing methods, such as drop casting and spin coating, it is difficult to control the uniformity and roughness of coating thickness, which affects the service life and sensing properties of gas sensors. The use of spray atomization technology can maximize the uniform dispersion of ink, and can control the amount of spray, concentration, height and other parameters to control the thickness and roughness of the coating.

Advanced Nanostructured Textile Catalysts for Enhanced Hydrogen Production in PEM Water Electrolysis: An Overview and Recent Developments

As the global focus shifts towards a zero-emission society, hydrogen has emerged as a critical element in various industries, particularly in green hydrogen production. A promising method for this is Polymer Electrolyte Membrane Water Electrolysis (PEMWE), which uses pure water and electricity to produce high-purity hydrogen. However, the efficiency of PEMWE is highly dependent on the effectiveness of its catalysts, particularly in the context of the catalyst-coated membranes (CCMs) employed in these systems. Conventional preparation of these CCMs involves multiple steps, including synthesis and application of a catalyst ink, which often leads to catalyst agglomeration and requires high Ir (Iridium) loadings to maintain uniformity and performance.In our latest study, we have developed a novel approach using ultralight conductive IrO2 nanostructured textiles (NST) as a catalyst layer for PEMWE. This innovative method successfully circumvents the issue of electrically isolated inactive catalysts, a common problem with lower Ir amounts in traditional catalyst layers. By employing a process of sputtering IrO2 onto water-soluble polymer nanofibers, we have achieved facile CCM preparation and demonstrated unprecedented long-term hydrogen evolution with ultra-low Ir mass loadings at high rates. Our study revealed that the high performance of these CCMs is derived from their low resistivity and unique porous three-dimensional structure.The preparation of NST involves dissolving polyvinylpyrrolidone (PVP) in methanol, followed by electrospinning this solution onto a metal-foil collector. The resulting PVP nanofibers then undergo a sputtering process to deposit IrO2, forming the nanostructured textiles. This method eliminates the need for wet chemical routes and labor-intensive processes typically associated with conventional catalyst layer preparations, thus offering a more environmentally friendly and scalable alternative.Our performance evaluations of these NST CCMs, with varying Ir mass loadings, have shown significant advancements. The operational cell voltages of CCMs containing as little as 0.05 mg-Ir cm−2 were suppressed across all investigated current densities compared to conventional CCMs. Notably, operational voltages remained below 2 V even at the highest current density of 7 A cm−2. This level of performance is unprecedented for CCMs with such low catalyst amounts. Additionally, the long-term stability of these CCMs was remarkable, with operational times exceeding 1500 hours without significant increases in voltage, showcasing their potential for practical applications.An essential aspect of our study was the analysis of the electrical properties and the surface structure of the IrO2 NSTs. We observed that the electrical conductivity of these textiles was significantly higher than that of conventional catalyst layers. This high conductivity, coupled with the unique interconnected structure of the textiles, ensures efficient electrical contact between nano catalysts and the current collector, thus avoiding the formation of isolated catalysts. Our analyses revealed that the IrO2 NSTs have unique surface terminations and a high number of undercoordinated surface Ir atoms, contributing to their high intrinsic catalytic activity.Further insights were gained through operando X-ray absorption spectroscopy (XAS) measurements, which showed that the IrO2-nanostructured textiles possess a large number of D-band holes and are intrinsically highly active. This finding is crucial as it links the unique chemical state of the textiles to their high activity in oxygen evolution reactions (OER), a key process in PEMWE.Our recent developments in nanostructured textile catalysts for PEMWE mark a significant leap in hydrogen production technology. By demonstrating high-rate hydrogen production at low operational voltages and with significantly lower Ir mass loadings compared to conventional CCMs, we have addressed major challenges in the field. These advancements not only enhance the efficiency and sustainability of hydrogen production but also open avenues for applying this technology to other electrochemical conversion cells, paving the way for broader applications and further research. In this talk, we discuss the latest activity on NST, and highlight the challenges and opportunities for hydrogen production.

Synthesis and Characterization of Electrospun Ni-BZY Nano-Fiber Anodes

Solid oxide fuel cell (SOFC) and related Protonic Ceramic Fuel Cell (PCFC) technologies have demonstrated significant promise for the efficient and clean electrochemical conversion of stored energy held in a wide variety of renewable fuels, decreasing dependence on traditional fossil fuels. The high efficiencies of both devices arise from the direct chemical-to-electrical energy transformation, achieved without moving parts and the losses inherent to combustion technologies. As in all fuel cells, electrons are generated via oxidation of fuel at the anode to power an external load before returning to the cathode to reduce an oxidant, usually O2. Separating the two electrodes is a dense, gas-tight, electronically insulating electrolyte that permits ion diffusion to complete the circuit. The SOFC’s solid oxide electrolyte passes oxides from the cathode to the anode, but the large activation barrier associated with this process requires high operating temperatures (≥700 ˚C), exacerbating degradative processes and adding challenges for thermal management. In contrast, the PCFC’s perovskite electrolyte permits protonic diffusion from the anode to the cathode, with a smaller activation barrier leading to lower operating temperatures (450 – 700 ˚C). Despite recent advancements in emerging PCFC materials, the overall efficiency and long-term stability of the device is still impacted in part by the anode’s ability to catalyze fuel oxidation, generate protons, and shuttle electrons to an attached current collector. These processes in turn are strongly linked to the morphology and stability of the anode—often a cermet composed of a Ni catalyst/electronic conductor and protonic ceramic such as yttrium-doped barium zirconate (BZY). In particular, continuity is needed for the Ni, BZY, and pore networks while maximizing boundaries between each phase (three-phase boundary). Traditionally, anodes are fabricated by mixing appropriate powders together without much control over the morphology over the micron-sized components. In this study, we explore an alternative approach to systematically engineer Ni-BZY nanofibers within the anode to enhance overall device performance through improving the underlying electrochemical processes at the anode. Low nickel-content BZY anodes (<40 wt. % Ni) for PCFCs are fabricated through electrospinning, with two distinct methods evaluated for nickel loading. First, uniform BZY nanofibers are synthesized by electrospinning a gel containing BZY metal cations and 5 wt. % Polyvinylpyrrolidone (PVP) as dispersant in ethanol/acetic acid solution followed by sintering at 900°C for 3 h in air, and subsequent electroless deposition of nickel on the fiber surfaces. Second, Ni-BZY is prepared by electrospinning a polymer containing a nickel salt and the same BZY precursors followed by co-sintering at 900°C for 3 h. The Ni-BZY fibers underwent morphological, crystallinity and elemental characterization via SEM, XRD, TEM and Raman microscopy. Initial comparison of the fibers fabricated by both methods has shown that uniform nickel loading of ~35 wt. % on the fibers was achieved in the second method. Slurries containing fibers made from both methods are deposited as anodes onto BZY electrolytes, and the complete cells are tested electrochemically under hydrogen at elevated temperature and compared with a control PCFC constructed using conventional powder materials with comparable nickel loading. In summary, electrospun nanofibers, known for their excellent permeability and faster charge transfer due to their porous structure, present an intriguing alternative for high-performance PCFC anode materials. Figure 1

Micropatterning MXene/TiO2 Nanocomposite Ink for Gas Sensing

This work describes the preparation, characterization and micropatterning of MXene (Ti3C2/TiO2) nanocomposite inks. The MXene nanopowder was oxidized to Ti3C2/TiO2 nanocomposite powder by stirring in air for 3 hours using air aging method. The Ti3C2/TiO2 nanocomposite powder was then dispersed into Dimethyl Sulfoxide (DMSO) solvent, and the Ti3C2/TiO2 ink was prepared by using 1% mass fraction of Polyvinylpyrrolidone (PVP) solution as dispersant. The two-dimensional layered nanostructure of MXene and the characteristic peaks of TiO2 were observed by Raman and XRD results. SEM and TEM results show the layered structure of MXene nanoparticles as well as TiO2 nanoparticles with a diameter of about 2 nm on a single layer of MXene. FTIR results confirms that Ti-O bonds and Ti-C bonds indicating that part of Ti3C2 was oxidized to TiO2. The results of Brunauer Emmett Teller (BET) test on Ti3C2/TiO2 nanocomposite ink show that the specific surface area of the ink is 10.7194 m²/g and the maximum adsorption of N2 is 32.039cm3/g. Thermogravimetric analysis (TGA) indicate that Ti3C2/TiO2 exhibited excellent thermal stability, with a mass loss of only 15% at 800°C. In order to achieve the optimal printing effect, plasma surface treatment was carried out on the gold-plated silicon wafers, Polyethylene terephthalate (PET), and glass substrates, which decreases the contact angle of the ink on these substrates. The printing of Ti3C2/TiO2 nanocomposite ink on the substrate using the atomized printing technique with a mask plate enables printing of straight lines with a line width of 5µm. Film thickness can be controlled by adjusting the distance between the printhead and the substrate, as well as the pressure of the atomized printing jet.

Characterization, impact and wear properties of treated and as-received graphene nanosheets reinforcement in epoxy resin composites

PurposeThis study aims to explore the enhancement of mechanical properties in epoxy resin composites through the incorporation of graphene nanoparticles, focusing on their impact and wear resistance. It investigates the role of graphene, both treated and untreated, as a reinforcing agent in composites, highlighting the significance of nanoparticle dispersion and surfactant treatment in optimizing mechanical performance.Design/methodology/approachEmploying a novel dispersion technique using a drawing brush, this research contrasts with traditional methods by examining the effects of graphene nanoparticle concentrations treated with surfactants – Polyvinylpyrrolidone (PVP) and Sulphonated Naphthalene Formaldehyde (SNF) – on the mechanical properties of epoxy resin composites. The methodology includes conducting a series of impact and wear tests to assess the influence of graphene reinforcement on the composites' performance.FindingsThe findings reveal a marked enhancement in the composites impact resistance and energy absorption capabilities, which escalate with an increase in graphene content. Additionally, the study demonstrates a significant improvement in wear resistance, attributed to the superior mechanical properties, robust interface adhesion and effective dispersion of graphene. The use of surfactants for graphene treatment is identified as a crucial factor in these advancements, offering profound insights into the development of advanced composite materials for diverse industrial uses.Originality/valueThis study introduces a unique dispersion technique for graphene in epoxy composites, setting it apart from conventional methods. By focusing on the critical role of surfactant treatment in enhancing the mechanical properties of graphene-reinforced composites, it provides a novel insight into the optimization of impact and wear resistance.

Fat-signal suppression in breast diffusion-weighted imaging: the Good, the Bad, and the Ugly.

Fat-signal suppression is essential for breast diffusion magnetic resonance imaging (or diffusion-weighted MRI, DWI) as the very low diffusion coefficient of fat tends to decrease absolute diffusion coefficient (ADC) values. Among several methods, the STIR (short-tau inversion recovery) method is a popular approach, but signal suppression/attenuation is not specific to fat contrary to other methods such as SPAIR (spectral adiabatic (or attenuated) inversion recovery). This article focuses on those two techniques to illustrate the importance of appropriate fat suppression in breast DWI, briefly presenting the pros and cons of both approaches. We show here through simulation and data acquired in a dedicated breast DWI phantom made of vials with water and various concentrations of polyvinylpyrrolidone (PVP) how ADC values obtained with STIR DWI may be biased toward tissue componentswith the longest T1 values: ADC values obtained with STIR fat suppression may be over/underestimated depending on the T1 and ADC profile within tissues. This bias is also illustrated in twoclinical examples. Fat-specific methods should be preferred over STIR for fat-signal suppression in breast DWI, such as SPAIR which also provides a higher sensitivity than STIR for lesion detection. One should remain aware, however, that efficient fat-signal suppression with SPAIR requires good B0 shimming to avoid ADC underestimation from residual fat contamination. The spectral adiabatic (or attenuated) inversion recovery (SPAIR) method should be preferred over short-tau inversion recovery (STIR) for fat suppression in breast DWI. Fat-signal suppression is essential for breast DWI; the SPAIR method is recommended. Short-tau inversion recovery (STIR)is not specific to fat; as a result, SNR is decreased and ADC values may be over- or underestimated. The STIR fat-suppression method must not be used after the injection of gadolinium-based contrast agents.

Determining the critical time points for hydrate formation in the presence of kinetic hydrate inhibitors: A rheological and kinetic study

Kinetic hydrate inhibitors have the characteristics of delaying hydrate nucleation and reducing hydrate growth rate. The utilized of kinetic hydrate inhibitors for hydrate blockage risk management is a promising technology for hydrate prevention in oil and gas industry. In this study, the rheological and kinetic properties of gas–water systems contained pure water, polyvinyl pyrrolidone and newly-synthesized inhibitor during hydrate formation at different subcooling degrees were in situ characterized using a high-pressure rheometer. By analyzing the experimental results, the concept of ‘critical time’ have been proposed to divide the time-varying process of hydrate formation into multiple stages. The three critical times indicated distinct trends in viscosity and pressure changes, as well as varying risks of hydrate blockage in hydrate prevention. The results further compared the differences in determining critical time through pressure and viscosity. The critical time of hydrate nucleation determined by viscosity was earlier than pressure due to the hypothesis of lag in gas consumption. The critical time of rapid hydrate growth determined by viscosity was later than gas consumption, which may be due to that the sharp increase in viscosity requires the aggregation of hydrates. According to the inhibition effect evaluation results determined by three critical times, it was found that the newly-synthesized inhibitor was more effective than polyvinyl pyrrolidone in inhibiting nucleation, delaying rapid hydrate growth time and reaching high viscosity time. This study can provide a comprehensive evaluation method for assessing the performance of kinetic hydrate inhibitors from both kinetic and rheological perspectives.

Microstructure evolution of zirconium boride whiskers prepared by electrospinning and their toughening effect

AbstractZirconium boride (ZrB2) whiskers hold significant potential for toughening ultra‐high temperature ceramics (UHTCs). Yet, their fabrication remains challenging due to limited knowledge of the microstructure evolution. Herein, high‐purity ZrB2 whiskers were successfully prepared by electrospinning combined with carbothermal reduction. Specifically, a precursor solution containing Zr–O–C–B networks stabilized through hydrogen bonds with polyvinyl pyrrolidone was synthesized as a spinnable ZrB2 precursor. High‐purity ZrB2 whiskers with a diameter of ca. 200 nm and a length of 5–10 µm were obtained by precise heat treatment of ZrB2 precursor fibers. In this process, ZrO2 grains formed initially and transformed into ZrB2 grains through carbothermal reduction, which further converted into ZrB2 whiskers through a solid‐liquid‐solid mechanism. To testify to the toughening effect for UHTCs, the ZrB2 whiskers were added into ZrB2 powders and followed by sintering. This strategic addition of 5 wt% ZrB2 whiskers led to a 19% enhancement in the fracture toughness of ZrB2 bulk. This study illuminated the preparation strategy and formation mechanism for ZrB2 whiskers and their application for toughening UHTCs.

Development of Ionic Polymer Membrane Based on PVDF for Capacitor Application

Objective: To address these issues, we propose the use of ionic polymer membranes. By reducing the demand for synthetic plastics, these membranes contribute to pollution reduction. Moreover, they offer economic and environmental benefits. Ionic polymers can also help limit carbon dioxide emissions. Method: In our study, we created a blend of polyvinylidene fluoride (PVDF), polyvinylpyrrolidone (PVP), and polyvinyl sulfonic acid (PVSA). This blend was used to fabricate an ionic membrane through the solvent casting method. The resulting membrane acts as a successful dielectric material, sandwiched between copper electrodes. We conducted extensive characterization, including microstructure analysis, crystal structure examination, identification of functional groups, and thermal behavior assessment. Results: Our findings demonstrate the potential of ionic polymer membranes for capacitor applications. By varying the composition of PVDF/PVP/PVSA, we explored different dielectric properties. Notably, the ionic polymer electrolyte can serve as an effective dielectric material, with copper electrodes providing a practical application. Conclusion: Our investigation included electrical current density measurements using cyclic voltammetry, elemental composition analysis, morphological studies, and material composition assessments.

Development of hybrid polyvinylpyrrolidone/carboxymethyl cellulose/collagen incorporated oregano scaffolds via direct ink write printing for potential wound healing applications

Additive manufacturing can develop regenerative scaffolds for wound healing. 3D printing offers meticulous porosity, mechanical integrity, cell adhesion and cost-effectiveness. Herein, we prepared ink composed of carboxymethyl cellulose (CMC), polyvinylpyrrolidone (PVP), collagen, and oregano extract for the fabrication of tissue constructs. The blend was optimized to form a homogeneous ink and rheological characterization demonstrated shear thinning behavior. The scaffolds were printed using Direct Ink Write (DIW) at a flow speed of 4 mm3/s and a layer height of 0.18 mm. The fabricated scaffolds demonstrated an ultimate tensile strength (UTS) and toughness of 730 KPa and 2.72 MJ/m3, respectively. Scanning Electron Microscopy (SEM) revealed an average pore size of 300 ± 30 μm. Fourier transform infrared spectroscopy (FTIR) analysis confirmed that all materials were present. The contact angle of the composite scaffold was 68° ± 1°. Moreover, the scaffolds presented 82 % mass loss (degradation) in phosphate buffer saline (PBS) over 14 days. The composite scaffold exhibited inhibition zones of 9 mm and 12 mm against Staphylococcus aureus and Escherichia coli, respectively. The PVP/CMC/collagen/oregano 3D printed scaffolds exhibited excellent biocompatibility with the mesenchymal stem cells and humman dermal fibroblast cells, confirmed by water-soluble tetrazolium - 8 (WST-8) assay (test conducted for 7 days). The enhanced angiogenic potential of said scaffold was assesed by release of vascular endothelial growth factor followed by further validation through in-vivo CAM assay. Thus, confirming suitability for the potential wound healing application.

Antibacterial and antioxidant phlorizin-loaded nanofiber film effectively promotes the healing of burn wounds.

Burns usually result in damage and loss of skin forming irregular wound wounds. The lack of skin tissue protection makes the wound site highly vulnerable to bacterial infections, hindering the healing process. However, commonly used wound dressings do not readily provide complete coverage of irregular wounds compared to regular wounds. Therefore, there is an urgent need to prepare a wound dressing with high antimicrobial efficacy for the administration of drugs to irregular wounds. In this study, a chitosan (CS)/polyvinylpyrrolidone (PVP) composite nanofiber membrane (CS/PVP/Phlorizin) loaded with root bark glycosides (Phlorizin) was developed using an electrostatic spinning technique. The incorporation of phlorizin, a natural antioxidant, into the fiber membranes notably boosted their antimicrobial and antioxidant capabilities, along with demonstrating excellent hydrophilic characteristics. In vitro cellular experiments showed that CS/PVP/Phlorizin increased Hacat cell viability with the presence of better cytocompatibility. In scald wound healing experiments, Phlorizin-loaded nanofibrous membranes significantly promoted re-epithelialization and angiogenesis at the wound site, and reduced the inflammatory response at the wound site. Therefore, the above results indicate that this nanofiber membrane is expected to be an ideal dressing for burn wounds.

Polyvinylpyrrolidone-assisted sol–gel synthesis of efficient Li2TiSiO5/C composite anodes for Li-Ion batteries

This study presents the process of developing an effective anode material for lithium-ion batteries (LIBs) by usage of Li2TiSiO5 coated with a thin layer of carbon (LTSO/C). The material was prepared through a sol–gel method, where varying amounts of polyvinylpyrrolidone (PVP) were used as a carbon source during the synthesis process. The physicochemical analysis of the LTSO/C samples indicates that as the amount of PVP used during sol–gel synthesis increases, the particle diameter of LTSO decreases. Furthermore, the analysis shows that a thin amorphous carbon layer is deposited on the LTSO surfaces, along with additional carbon networks between the LTSO particles. Based on the electrochemical analysis conducted to optimize the amount of PVP during synthesis, the resulting LTSO/C composite electrode synthesized with 1 g of PVP exhibits a specific capacity of 274.5 mAh·g−1 at 0.1C after 150 cycles, which is quite close to the theoretical capacity. In addition, this LTSO/C electrode demonstrates exceptional electrochemical performance when operated at high rates, surpassing a discharge capacity of 170 mAh g−1 up to 2C. Therefore, the LTSO/C is an excellent choice for high-performance anode material in LIBs.