Amorphous Research Articles

Nano ZnO modified amorphous carbon materials enabling long-cycle performance and high-capacity for lithium/sodium-ion batteries

Zinc-modified carbon materials exhibit high specific capacity, good safety, and low self-discharge, making them promising anode materials for lithium-ion and sodium-ion batteries. However, the high cost of raw materials, complex fabrication processes, and limited cycle life remain significant challenges to their further development. In this study, we elucidated a two-step process, simple in technique and suitable for large-scale production, for in-situ zinc modification of amorphous carbon. The synthesized carbon material exhibited superior reversible specific capacity (maintaining 780.27 mAh·g−1 capacity after 80 cycles at 50 mA·g−1 current density), high cycling stability (maintaining Coulombic efficiency at 100.06 % after 15,000 cycles at 10 A·g−1 current density), and good application value (achieving a capacity of 89.67 mAh·g−1 after 1000 cycles at 200 mA·g−1 current density for the assembled MFAC-Zn || NVP full cell). Through our investigation, we discovered that Nano ZnO not only directly participate in electrochemical reactions but also effectively improve the microstructure of amorphous carbon, increasing its three-dimensional axial stacking and providing more reaction sites. The enrichment of open pores significantly enhances the diffusion efficiency of ions within the carbon-based matrix. The superior diffusion ability of alkali metal-ion in the electrode is the reason for the excellent electrochemical performance of Zinc-modified amorphous carbon. Moreover, the incorporation of Nano ZnO aids in the formation of a robust and thin SEI layer. This significantly enhances the stability of the electrode materials during cycling and improves charge transfer efficiency during the charge-discharge process. Our study provides a new strategy for adjusting the internal microstructure of amorphous carbon materials to achieve high-performance lithium/sodium storage.

Advanced Study of Structural and Optical Characteristics of Nanocrystalline Coomassie Brilliant Blue G-250 for Optoelectronic Device Optimization

This study explores the structural and optical properties of Coomassie Brilliant Blue G-250 (CBBG) using X-ray diffraction (XRD) and spectroscopic techniques. XRD analysis of both powder and thin film samples reveals distinct structural features: the powder exhibits a polycrystalline structure with strong diffraction peaks corresponding to cubic lattice planes, while the thin film shows a mix of crystalline orientations within an amorphous matrix. The Williamson-Hall relation is applied to determine average crystallite sizes, yielding 85.5nm for the powder and 71.8nm for the thin film, indicating their nanocrystalline nature. Microstrain analysis also reveals compressive strain within the thin film. These structural insights are critical for understanding CBBG's mechanical and optical properties, vital for biochemical and optoelectronic applications. Density functional theory (DFT) calculations with the B3LYP/6-311++G(d,p) basis set were used to optimize the molecular geometry and analyze HOMO-LUMO energies and reactive sites via the MEP map. CBBG shows higher hyperpolarizability than urea, indicating its potential for nonlinear optical applications. Miller indices further support its optoelectronic optimization. The real (ε1) and imaginary (ε2) parts of the dielectric constant were analyzed, revealing CBBG thin films exhibit strong polarization and charge displacement, influenced by structural disorder. Additionally, the volume and surface energy loss functions (VELF and SELF) highlight significant internal energy dissipation, emphasizing CBBG's potential for optoelectronic devices. The complex optical conductivity analysis reveals key absorption and dispersion behaviors essential for advanced photonic and electronic device design.

Novel Fimasartan Fluidized Solid Dispersion and Its Tablet: Preparation, Crystallinity, Solubility, Dissolution, and Pharmacokinetics in Beagle Dogs.

Fimasartan, an angiotensin II receptor antagonist, exhibits low bioavailability due to its poor solubility; consequently, using solubilization technologies is essential to improve its bioavailability. In this study, novel fimasartan fluidized solid dispersion (FFSD) was developed using a fluid bed granulator to enhance the drug solubility andoral bioavailability. An appropriate FFSD was prepared in 50% ethanol using a fluid bed granulator, and its drug dissolution, morphology, and crystallinity were evaluated in comparison to the powdered drug. Moreover, the dissolution in various pH conditions and pharmacokinetics of the FFSD tablet in beagle dogs were investigated compared to the commercial fimasartan tablet. Among the hydrophilic polymers tested, hydroxypropyl methylcellulose (HPMC)showed the highest solubility. The FFSD, composed of fimasartan, HPMC, and microcrystalline cellulose at the weight ratio of 20:10:25, gave a granular aggregation of several particles with a smooth surface. The drug in this FFSD existed as an amorphous state, leading to a greatly increased drug dissolution. The FFSD tablet was prepared by compressing a mixture of FFSD, mannitol, croscarmellose sodium, and magnesium stearate at the weight ratio of 55:40:5:1. The FFSD tablet gave significantly higher drug dissolution, plasma concentrations, maximum plasma concentration (Cmax) andarea under the whole blood concentration-time curve (AUC) values than did the commercial fimasartan tablet. In the beagle dogs, the FFSD tablet (140.39±27.40ng·h/ml) had about a 1.7-fold higher AUC than the commercial fimasartan tablet (80.58±22.18 ng·h/ml), indicating an enhancement in thebioavailability. This novel FFSD tablet could be a potential oral pharmaceutical product with the improved oral bioavailability of fimasartan.

Recording and Revealing 2.5D Nanopatterned Hidden Information on Silk Protein Bioresists.

Nanopatterning on biomaterials has attracted significant attention as it can lead to the development of biomedical devices capable of performing diagnostic and therapeutic functions while being biocompatible. Among various nanopatterning techniques, electron-beam lithography (EBL) enables precise and versatile nanopatterning in desired shapes. Various biomaterials are successfully nanopatterned as bioresists by using EBL. However, the use of high-energy electron beams (e-beams) for high-resolutive patterning has incorporated functional materials and has caused adverse effects on biomaterials. Moreover, the scattering of electrons not absorbed by the bioresist leads to proximity effects, thus deteriorating pattern quality. Herein, EBL-based nanopatterning is reported by inducing molecular degradation of amorphous silk fibroin, followed by selectively inducing secondary structures. High-resolution EBL nanopatterning is achievable, even at low-energy e-beam (5keV) and low doses, as it minimizes the proximity effect and enables precise 2.5D nanopatterning via grayscale lithography. Additionally, integrating nanophotonic structures into fluorescent material-containing silk allows for fluorescence amplification. Furthermore, this post-exposure cross-linking way indicates that the silk bioresist can maintain nanopatterned information stored in silk molecules in the amorphous state, utilizing for the secure storage of nanopatterned information as a security patch. Based on the fabrication technique, versatile biomaterial-based nanodevices for biomedical applications can be envisioned.

Microencapsulation of Ferrous Sulfate in Lipid Matrices Produced by Spray Chilling: Characterization, Controlled Release, and In Vitro Gastric Behavior

ABSTRACTIron deficiency is a global nutritional concern, and food fortification is a strategy to address it. However, direct iron fortification can negatively impact sensory attributes. Spray chilling microencapsulation offers a solution while enhancing iron bioavailability. This study aimed to produce iron‐containing microparticles using spray chilling with varying ratios of beeswax and cocoa butter. The ratios had minimal impact on overall yield (73%–75%). The microparticles exhibited β and β′ polymorphic forms, and the inclusion of cocoa butter led to a more amorphous and heterogeneous matrix, resulting in more complex thermal behavior. Higher cocoa butter content improved iron retention (79%–81%) compared with higher beeswax concentrations (69%–70%). LPMs with greater cocoa butter content exhibited reduced iron release, with release kinetics following diffusion and relaxation mechanisms. Iron release across different temperatures ranged from 0.11 to 0.42 mg L−1, influenced by the lipid matrix, particle distribution, and size. The highest release was attributed to smaller, more homogeneous particles containing only one lipid in the matrix. LMPs effectively protected iron release under simulated gastric conditions, allowing significant release in simulated intestinal conditions (36.1%–56.3%). These iron microparticles show potential for use in the food industry, particularly for fortifying various food products, including infant formulas and supplements.

A core-shell structured crystalline@amorphous MnO2 with enhanced plasma catalytic degradation performance for volatile organic sulfur compounds and degradation mechanism exploration

A crystalline@amorphous MnO2 (HT@RT) plasma catalyst was successfully constructed in this study to address the problem of odor pollution, especially from volatile organic sulfur compounds (VOSCs) with low olfactory thresholds. Complete conversion of dimethyl sulfide (DMS) at 140 J/L was achieved, and the ozone concentration in the exhaust gas was maintained below 5 ppm. Deeper mineralization of DMS was achieved in the HT@RT sample than in the individual HT and RT samples. A comprehensive analysis of multiple characterization techniques revealed that the HT@RT sample exhibited excellent DMS adsorption capacity, appropriate electric field responsiveness, high oxygen vacancy content, and abundant reactive oxygen species, which play key roles in the degradation of DMS. In addition, the DMS degradation process was investigated using in situ plasma diffuse reflectance infrared Fourier transform (DRIFT) spectroscopy. Combined with the results of gas chromatography-mass spectrometry, degradation pathways for DMS were proposed. The HT@RT sample combined the advantages of both amorphous and crystalline materials, significantly enhancing the activity and stability of the catalyst. Therefore, the crystalline@amorphous structured catalysts constructed in this study not only offer new insights for improving the performance of plasma catalysis but also provide an effective solution for eliminating odorous gases.

Eutectic binary phase diagram and kinetically stable homogeneous co-amorphous mixtures of two imidazole drugs

Amorphous multicomponent formulations allow improving the solubility and thus the bioavailability of active pharmaceutical ingredients (APIs) that are poorly soluble in water, provided that the molecular mobility in such formulations does not promote crystallization in the amorphous (glassy) state during their shelf life. Multicomponent formulations may involve a single API mixed with excipients, but also two mutually compatible APIs. Here, we describe kinetically stable amorphous binary mixtures of two commercial antifungal imidazole APIs, bifonazole and clotrimazole, which have similar melting points and glass transition temperatures. The equilibrium phase diagram of this binary system, as determined by differential scanning calorimetry, follows the Schroeder-van Laar-LeChatelier predictions, as typically found for compounds that are miscible as liquids but immiscible in the crystalline form, and is characterized by an experimental eutectic composition close to equimolar composition (xbifonazole = 0.45) and eutectic melting point Te = 392 K. The glass transition temperature Tg varies linearly with composition, as found in ideal liquid mixtures. Dielectric spectroscopy characterization is carried out to investigate the relaxation dynamics of each amorphous API separately, and of the amorphous mixtures (both in the supercooled liquid and glass state). A single structural α relaxation is observed in all supercooled liquid mixtures, confirming their homogeneity. Both pure amorphous APIs display conformational secondary relaxations: the one of bifonazole stems from the torsional rotation of the imidazole ring; the one of clotrimazole is significantly slower than that of bifonazole, and is related to small-angle librations of the imidazole and chlorobenzene rings. Conformational relaxation processes are observed also in binary mixtures, which display also a Johari-Goldstein relaxation as pure clotrimazole. Despite the presence of both primary and secondary relaxations, the binary mixtures are observed to remain amorphous for at least twelve months both at Tg and slightly above it.

INFLUENCE OF FIRECLAY GRANULES ON CALCIUM ALUMINATE CEMENT HYDRATION AND PROPERTIES AFTER FIRING

The article investigates the effect of granules, produced from dispersive fireclay using liquid glass as a binder, on the hydration process of calcium aluminate cement (CAC). Peculiarities of the hydration process were evaluated from the results of calorimetry, thermal analysis, XRD, SEM, and mechanical properties tests, as well as the relative viscosity of the cement pastes. It is determined that the granules are capable of entrapping water and releasing it later, shortening the incubation period and increasing the maximal heat release rate during the CAC crystallization stage and total cumulative heat as compared with the control samples with the same active cement part and containing dispersive fireclay particles, which are cement-inert. The redistribution of water due to granules’ addition results also in more hydrates C2AH8 and AH3 in CAC pastes containing granules than in those containing dispersive fireclay. Due to the reaction between the water solution containing dissolved cement minerals and sodium silicate film (dried liquid glass), the hydrogel-like phases form inside the granule during the hydration, which fill the gaps between the fireclay particles and after firing at 1100 °C form a glassy phase enveloping the fireclay particles and binding them to each other, providing the granule integrity and contributing to their strength. The specific structure formed due to the addition of fireclay granules does not change dramatically the density of the obtained composite, provides 7.4–18.5% higher strength after drying with 7.5–15% granule addition and ∼11% higher strength after sintering at 1100 °C with 5% granule addition (as compared with compositions containing dispersive fireclay). 30% granule addition can be considered as too much, causing significant strength loss.

A stress test method of polycrystal 95%Al2O3 based on Vickers indentation-induced cracks

IntroductionPolycrystalline alumina is a critical material in the containment of nuclear reactors, and its stress must be evaluated. ObjectiveThe current Vickers fracture residual stress test methods are mainly used for amorphous materials. To realize the preliminary application in engineering practice, exploring suitable stress test methods for polycrystalline alumina and testing the micro-zone stress of 95%Al2O3 in 4J33/95%Al2O3brazed joints is necessary. MethodsThe specimens were loaded with different stress states by pre-stressing tooling, and the stress distribution in the test area was clarified through finite element analysis. Then, Vickers indentation experiments were carried out to count the indentation radius a, the crack length l, and the direction of crack propagation θ. ResultsWith the crack size not exceeding the grain size and the effects of microstructure (intergranular pores, intragranular pores, and grain boundaries) and crystal orientation on the crack projection length reduced, a model was developed for calculating the relationship between the crack projection length and the pre-stress of polycrystalline alumina at low load indentation in Palmqvist, with a maximum absolute deviation of 23.3 MPa and a maximum relative error of 49.7 %. The microzone stresses on the ceramic side of 4J33/95 % Al2O3brazed joints were characterized. ConclusionThe stress detection method based on Vickers indentation cracks proposed in this study provides a new idea for evaluating residual stresses in polycrystalline alumina; however, the universality of this method in polycrystalline alumina with different grain sizes and its applicability in other polycrystalline brittle materials can still be further explored.

Extended Tauc-Lorentz Model for Amorphous Materials With Non-Exponential Band Tails

Extended Tauc-Lorentz Model for Amorphous Materials With Non-Exponential Band Tails

Green Synthesis, Characterization and Pharmaceutical Applications of Biocompatible Zinc Oxide Nanoparticles Using Heliotropium rariflorum Stocks.

Background: Zinc oxide nanoparticles are safe, non-toxic, and biocompatible. These NPs are used in food packaging materials, self-cleaning glass, ceramics, deodorants, sunscreens, paints, coatings, ointments, lotions, and as preservatives. This study explored the biological potential of ZnO nanoparticles synthesized using H. rariflorum. Methods: In vitro antibacterial and antifungal activities against Bacillus subtilis, Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, Salmonella typhi, Candida albicans, Penicillium notatum, Aspergillus flavus, Aspergillus niger and Aspergillus solani were determined. Antioxidant activity was explored using the DPPH radical scavenging method. In vivo analgesic, antipyretic and sedative potential of synthesized nanoparticles was investigated using a mouse model. Results: SEM with various magnification powers showed that some particles were spherical while some were aggregated, flake-shaped, and hexagonal with rough and irregular surfaces. The EDX analysis revealed Zn (12.63%), O (22.83%) and C (63.11%) with trace quantities of Si (0.40%), Ca (0.54%) and P (0.49%). The XRD pattern indicated an amorphous state, with no peaks observed throughout the spectrum. The UV-visible spectrophotometry revealed a characteristic absorption peak at 375 nm, indicating the presence of ZnO nanoparticles. Fourier Transform Infrared Spectroscopy (FTIR) displayed several small peaks between 1793 and 2370 cm-1, providing evidence of the presence of different kinds of organic compounds with different functional groups. ZnO-NPs showed dose-dependent antibacterial and antifungal potential against all strains. Staphylococcus aureus and Candida albicans were the most susceptible strains. The nanoparticles exhibited a maximum antioxidant effect of 85.28% at 100 μg/mL. In this study, the acute toxicity test showed no mortality, and normal behavior was observed in mice at ZnO-NP doses of 5, 10, and 20 mg/kg. For analgesic and antipyretic activities, a two-way ANOVA revealed that dose, time, and the interaction between dose and time were significant. In contrast, the samples had a non-significant effect on sedative activity. Conclusions: This innovative study suggests a potential use of plant resources for managing microbes and treating various diseases, providing a scientific basis for the traditional use of H. rariflorum.

Partial crystallization in Pd-BMG systems: From understanding structure towards influencing functionality through temperature-time series

Small quantities of crystalline domains created in an amorphous matrix are seen as an active driver for enhanced properties in bulk metallic glasses (BMGs). We investigated partial crystallization and phase transformations through a series of isotherms at 370°C performed on amorphous Pd-based BMG samples with the nominal composition of Pd43Cu27Ni10P20 (Pd-BMG) and a density of 9.425 g/cm3. X-ray based methods such as X-ray diffraction (XRD) and phase enhanced micro-computed tomography (μ-CT) have been pushed to their limits for studying atomic structure and morphology, while time available before crystallization has additionally been investigated via differential scanning calorimetry (DSC), and are combined with optical microscopy (OM), scanning electron microscopy (SEM), and hardness measurements for their mechanical properties. We reveal that Pd-based BMG samples isothermally treated at 370 °C start to crystallize after 20 min and still undergo phase transformations and recrystallization even after being fully crystalline after 60 min of the isothermal treatment. Interestingly, 3D phase enhanced micro-computed tomography shows a clear separation of two domains of slightly different densities. We highlight X-ray tomographic scans, allowing the 3D spatial visualization of extremely low-density contrast in different material domains, thus providing a multi-scale physical description of the Pd-BMG system. Interesting is the fact, that the re-crystallization is not homogenous and the crystalline domains can reach large size of (100–200 μm) in an amorphous matrix.

Single‐Luminophore Molecular Engineering for Rapidly Phototunable Solid‐State Luminescence

AbstractSmart materials enabling emission intensity or wavelength tuning by light stimulus have attracted attention in cutting‐edge fields. However, due to the general limitation of the dense molecular stacking (in solid states, especially in crystals) on photoresponsivity, constructing rapidly phototunable solid‐state luminescent systems remains challenging. Herein, we present a new luminophore that serves as both a photoresponsive and a luminous group with enhanced conformational freedom to attain this goal, namely, relying on photoexcitation‐induced molecular conformational change of an ionized persulfurated arene based on weak intermolecular aliphatic C−H⋅⋅⋅π interaction. Together with the phosphorescence characteristic of the molecule itself, rapidly enhanced phosphorescence upon irradiation can be observed in a series of phase states, like solution state, crystal, and amorphous state, especially with a high photoresponsive rate of 0.033 s−1 in crystal state that is superior to the relevant reported cases. Moreover, a rapidly phototunable afterglow effect is achieved by extending this molecule into some polymer‐based doping systems, endowing the system with unique dynamic imaging and fast photopatterning capabilities. This single‐luminophore molecular engineering and underlying mechanism have implications for building other condensed functional materials, principally for those with stimuli responses in solid states.

Modeling of fluence-dependent hole-burned spectra and hole-growth kinetics using multiple two-level system model.

Numerical formalism is presented that perfectly describes resonant low-temperature hole-burned spectra (including zero-phonon holes, ZPHs) and spectral hole-growth dynamics of Al-phthalocyanine tetrasulphonate embedded in hyperquenched glassy water films over more than seven orders of fluence magnitude (0.4 µJ/cm2-5.9 J/cm2). Frequency changes during spectral hole-burning (HB) are traditionally explained with the help of a single extrinsic two-level-system (TLSext) associated with impurity molecules. The new multiple two-level system (n-TLSext) models and data analysis presented in this work show that each chromophore in an amorphous medium can couple with multiple independent TLSext, which maintain perfect photo-memory, allowing a full return of the photoproduct to the initial ("preburn") state. Modeling reveals that the experimentally observed narrow photoproduct peak at higher energies, in close vicinity of the zero-phonon hole (ZPH), reflects a dynamical feature of the HB process populating so-called "terminal" states (states that do not interact with laser excitation). Within the n-TLSext model, each chromophore possesses multiple possibilities to create a photoproduct when in interaction with the burning laser, i.e., chromophores can interact with burning laser-light multiple times until reaching the terminal states. Due to phonon-assisted absorption, terminal states are typically at higher energies than the ZPH, in agreement with the hole burned spectra reported for many molecules embedded in various amorphous solids. However, many HB systems reveal both blue- (high-energy) and red-shifted (low-energy) antiholes (i.e., photoproducts). We suggest that future modeling of resonant holes in various proteins using our n-TLSext model will provide more insight on the complexity of the protein energy landscape.

Elastic properties of Fe95-yNb2Mo2Cu1Siy-xBx (x=5-8, y=20-26) at % amorphous alloys

Amorphous materials exhibit complex atomic structures characterized by the absence of long-range order, in contrast to the well-defined periodicity of crystalline materials. This structural complexity is further pronounced in compositions such as FeMCuSiB (M = Nb, Mo, W and Ta), which incorporate elements with varying atomic radii and valencies. The Young's modulus of structures generated using traditional methods, such as melt-quenching and random packing, shows poor agreement with experimental data. In this study, we employ hybrid methods for generating the structures, which involve randomly packing elements without overlap, followed by thermalization at room temperature using Ab-initio Molecular Dynamics simulations. The Young's modulus evaluated from these structures aligns well with values measured using Dynamic Mechanical Analysis. Additionally, we utilize these structures to determine other elastic moduli including the bulk modulus and tetragonal shear modulus and find that the obtained values are consistent with the expected range for these compounds. We attribute the improved accuracy to a more representative approximation of the amorphous structure and the direct application of energy-strain relationships, rather than stress-strain relationships, for elastic moduli determination. Our methodology facilitates reliable predictions of the physical properties of amorphous materials and contributes to the design of FeMCuSiB (M = Nb, Mo, W and Ta) alloys with enhanced mechanical properties.

Amorphous Exsolution of Fe3O4 Nanoparticles in SrTiO3: A Path to High Activity and Stability in Photoelectrochemical Water‐Splitting

Exsolution creates metal nanoparticles embedded within perovskite oxide matrices, promoting optimal exposure, even distribution, and robust interactions with the perovskite structure. Fe3O4, an oxidized form of Fe, is an attractive catalyst for photoelectrochemical (PEC) water‐splitting due to its strong light absorption, excellent electrical conductivity, and chemical stability. However, exsolving Fe is challenging, often requiring harsh reduction conditions that can decompose the perovskite. Herein, hybrid composites are fabricated for PEC water‐splitting by reductively annealing a solution of SrTiO3 photoanode and Fe cocatalyst precursors. In situ transmission electron microscopy reveals uniform, high‐density Fe particles exsolving from amorphous SrTiO3 films, followed by film‐crystallization at elevated temperatures. This innovative process extracts entire Fe dopants while maintaining structural stability, even at doping levels exceeding 50%. Upon air exposure, the embedded Fe particles oxidize to Fe3O4, forming a Schottky junction and enhancing light absorption. These conditions yield a high activity of 5.10 mA cm−2 at 1.23 V versus reversible hydrogen electrode (an 11.86‐fold improvement over SrTiO3) from the 30% Fe‐doped SrTiO3, with excellent stability (97% retention) over 24 h. Theoretical calculations indicate that in the amorphous state, FeO bonds weaken while TiO bonds remain strong, promoting selective exsolution. The mechanisms driving amorphous exsolution versus crystal exsolution are elucidated.

High‐precision numerical simulation method for thermal–mechanical coupling in rubbers

AbstractImproving the precision of numerical simulations in thermal–mechanical coupling for amorphous polymer materials is crucial for their effective utilization. To enhance the precision of rubber numerical simulations, this study proposed a method considering the temperature and strain rate to establish tensile testing conditions based on the principle of time–temperature equivalence. Additionally, to obtain more precise parameters for hyperelastic constitutive equations, stress relaxation experiments were conducted to determine a set of stress values under complete rubber stress relaxation, which were used to fit the hyperelastic components of the hyper‐viscoelastic algorithm. A finite element model of rubber rebound was established, and a hyperelastic model based on loss factor and a hyperelastic model based on Prony series (hyper‐viscoelastic) were used to calculate the temperature changes caused by rubber rebound coefficient and energy dissipation during the rebound process at 110, 120, and 130°C. We compared the calculation results of these two algorithms with experimental data to verify their accuracy. The research results show that the average error of the rebound coefficient of the hyperelastic algorithm at three temperatures is 3.63%, and the average error of the rebound coefficient of the hyper‐viscoelastic algorithm at these three temperatures is 0.93%. The comparison with the rebound test results shows that the hyper‐viscoelastic method is more accurate and better captures the viscoelastic hysteresis of rubber, but the model calculation time is longer. In addition, at the moment of rebound sample impact, the maximum temperature rise amplitude of the hyperelastic algorithm sample impact position is 2.60, 1.75, and 0.91°C, which are 110, 120, and 130°C, respectively; The maximum heating amplitudes of the hyper‐viscoelastic algorithm are 2.05, 1.35, and 0.61°C. The hyper‐viscoelastic algorithm is closer to the actual test results.Highlights Applied the principle of time–temperature equivalence. Determination of material parameters using the hyper‐viscoelastic algorithm. Calculated the temperature change during the rubber rebound process.

Change of crystallinity and optical transmittance of K2Ni(SO4)2·6H2O single crystal by heat treatment

Potassium nickel sulfate hexahydrate (KNISH) was prepared and grown as single crystal from the supersaturated aqueous solution at 309 K using slow evaporation method. Thermal measurements were achieved for the prepared crystal. The dehydration process, structural phase transitions and melting point of the obtained material were detected. Crystal structure and optical transmittance of KNISH crystal were studied through heat treatment. At 370 K, the dehydration process started to convert KNISH to the anhydrous phase KNIS and the crystallinity decreased gradually until the material became totally amorphous at 383 K. The anhydrous KNIS stayed at the amorphous state from 383 K to 629 K where it transformed again to the crystalline state with different structure. The heat treatment under dehydration temperature did not affect the efficiency of KNISH crystal for using as ultraviolet light filter and sensor. Above dehydration temperature, the obtained anhydrous phase KNIS is not suitable for these applications.

Investigating Charge-Induced Transformations of Metal Nanoparticles in a Radically-Inert Liquid: A Liquid-Cell TEM Study.

We present a novel in situ liquid-cell transmission electron microscopy (TEM) approach to study the behavior of metal nanoparticles under high-energy electron irradiation. By utilizing a radically-inert liquid environment, we aim to minimize radiolysis effects and explore the influence of charge-induced transformations. We observed complex dynamics in nanoparticle behavior, including morphological changes and transitions between amorphous and crystalline states. These transformations are attributed to the delicate interplay between charge accumulation on the nanoparticles and enhanced radiolysis, suggesting a significant role for charge-assisted processes in nanoparticle evolution. Our findings provide valuable insights into the fundamental mechanisms driving nanoparticle behavior at the nanoscale and demonstrate the potential of liquid-cell TEM for studying complex physicochemical processes in controlled environments.

Customizable Self-Microemulsifying Rectal Suppositories by Semisolid Extrusion 3D Printing.

Objectives: This study aims to create an innovative self-microemulsifying drug delivery system (SMEDDS) suppository for ibuprofen (IBU) using semisolid extrusion (SSE) three-dimensional (3D) printing technology. Methods: Based on solubility studies and the ability to form a transparent microemulsion upon dilution, a selected oil, surfactant, and co-surfactant were utilized to prepare SMEDDS-3DPS containing IBU. The optimal formulation consisted of 10% Triacetin, 80% Gelucire 48/16, and 10% Tetraethylene glycol. SSE 3D printing was employed to create three different-sized suppositories with varying drug contents. These suppositories were assessed for their physicochemical properties, content uniformity, and dissolution profiles. Results: The prepared mixture exhibited suitable physical properties for printing, with nano-sized emulsion droplets providing a large surface area for improved drug absorption in the rectum. Characterization techniques such as differential scanning calorimetry, powder X-ray diffraction, and Fourier transform infrared spectroscopy indicated that IBU was present in the formulation in an amorphous state. Additionally, in vitro dissolution tests demonstrated that SMEDDS-3DPS had a significantly higher initial dissolution rate compared with IBU powder. Conclusions: This research suggests that SMEDDS-3DPS, as a rectal IBU dosage form, can enhance the rectal bioavailability of IBU. It demonstrates the versatility of 3D printing as a novel manufacturing method for lipid-based suppositories and highlights the simplicity and adaptability of SSE 3D printing technology in producing customized suppositories tailored to individual patient needs, surpassing traditional methods.