Decrease In Transition Temperature Research Articles

Low dielectric properties of alkali-free aluminoborosilicate fiber glasses for PCB applications at 10GHz.

Alkali-free aluminoborosilicate glasses without (GDMC-Si) and with La2O3 addition (GDMC-La) were fabricated with an aim to develop low dielectric glass fibers for use in printed circuit boards (PCBs) as a reinforcing material in high-speed 5G/6G telecommunications application. This study presents the structural, thermo-physical, and dielectric properties of the glasses. The decrease in glass transition temperature (Tg) and the increase in coefficient of thermal expansion (CTE) were found by the addition of SiO2 and La2O3 in the present glass system, which are due to the depolymerization of the glass networks confirmed by the FTIR analysis. The dielectric constants (Dk) and the dissipation factors (Df) of the glasses were investigated at a high frequency of 10GHz. The Dk values of the GDMC-Si and GDMC-La glass systems reached a minimum of 4.50 and 4.75, while their Df values reached a minimum of 2.86 × 10-3 and 3.01 × 10-3, respectively. Notably, the Dk and Df values of the present glasses were lower than the commercial E-glass (Dk: 6.9, Df: 7.0 × 10-3 at 10GHz) and L-glass (Dk: 4.8, Df: 3.0 × 10-3 at 10GHz). Glass fibers with a diameter of 10μm were successfully drawn by the continuous melt-spinning process and their mechanical properties were investigated.

Investigation of electrochemical properties of lithium salt/poly(vinylidene fluoride)/polypyrrole blends

AbstractIn this study, structural, thermal, morphological, and electrochemical properties of poly(vinylidene fluoride)/polypyrrole (PVDF/PPy) blends are investigated. The investigation revealed phase separation between PPy and PVDF, a phenomenon supported by the thermodynamic interaction parameter. Increasing the PPy content from 10 to 50 wt% led to a significant reduction in the crystallinity of PVDF from 55.1% to 39.6%, and a corresponding decrease in the glass transition temperature (Tg) from 52.2 to 42.3°C. The enhanced interaction between components in the PVDF/PPy blends leads to an increase in local free volume due to the disruption of the polymer matrix. This disruption allows for greater molecular mobility, which in turn decreases the Tg. The increase in local free volume facilitates segmental motion of the polymer chains, thereby reducing the energy required for the transition from a glassy to a rubbery state. Ionic conductivity of the blends decreased with rising temperatures, likely due to interactions between the fluorine groups of PVDF and the NH groups of PPy. Notably, the transference number of lithium ions (tLi+) decreased from 0.30 to 0.14 as the PPy content increased from 10% to 50%, indicating a strong interaction between the cation and the polymer matrix.Highlights Electrochemical properties of poly(vinylidene fluoride)/polypyrrole (PVDF/PPy) blends are investigated. Interaction parameter‐supported phase separation is seen between PPy and PVDF. Intramolecular interactions of PVDF result in increasing local free volume. Ionic conductivity of the blends decreased with rising temperatures. tLi+ decreased with PPy increasing due to strong interaction of cation/matrix.

Influence of Bismuth Content on the Properties of Glass-Ceramics with Composition xBi2O3-(0.40-x)B2O3-0.15ZnO-0.45P2O5: Synthesis, Structural, Thermal Analysis, and Dielectric Relaxation Process

The glass-ceramics materials with the sample composition of xBi2O3-(0.40-x) B2O3-0.15ZnO-0.45P2O5 (BBZP) (where x = 0.10, 0.15, 0.20, and 0.25) have been prepared using the conventional melt-quenching technique. Different nanocrystalline phases embedded inside the glass-ceramic matrix have been characterised by analysing x-ray diffraction spectra. The obtained density values as well as molar volume increases with the rise of bismuth content. The network structure of the glass ceramic samples has been investigated employing Raman spectroscopy. The DSC analysis reveals the decrease in Glass transition temperature (Tg) (433K-416K), and crystallization temperature (Tc) (569K-556K) of the studied materials. The electrical properties of the samples have been investigated in the context of dielectric and modulus formalism. Different theoretical models have been employed to analyse the experimental data of dielectric and modulus spectra. The Nyquist plots of the materials have also been analysed employing relevant models. It has been shown that the higher bismuth containing samples are highly dense with high thermal stability. Such materials also have high dielectric strength. Analysis of these performance indicators suggests the possible applications of these materials in electrochemical devices.

Investigation of UV-blocking and photon-down conversion characteristics of PMMA@ CH3NH3PbBr3:WO3 polymer nanocomposites

Herein, methyl ammonium lead bromide: Tungsten trioxide (CH3NH3PbBr3:WO3) nano heterojunction and polymethyl methacrylate (PMMA) polymer composite films of different weight percentage (wt%) proportions of CH3NH3PbBr3:WO3 nanoparticles (0, 0.5, 1.0, 1.5 and 2.0 wt%) were prepared. The structure, morphology and thermal features of CH3NH3PbBr3:WO3 heterojunctions and PMMA@CH3NH3PbBr3:WO3 nanocomposites were investigated using X-ray diffraction (XRD), Fourier Transform-Infrared (FTIR) spectroscopy, Scanning electron microscopy (SEM) and Differential scanning calorimetry (DSC) techniques. The characterization data revealed decrease in crystallinity (up to 7.97%) and glass transition temperature (Tg) with increase in the concentration of CH3NH3PbBr3:WO3 nanoparticles in PMMA nanocomposites. The UV-visible absorbance and transmittance data of PMMA nanocomposites recorded using UV-visible spectroscopy was used to mathematically deduct the optical characteristics such as absorption coefficient, optical band gap, refractive index, extinction coefficient, finesse coefficient, optical conductivity and Urbach energy. The deducted data revealed improved UV-shielding, refractive index and optical conductivity values while the optical band gap and Urbach energy was found to decrease with concentration of dopant. The experimental data of different PMMA@CH3NH3PbBr3:WO3 composite films showed excellent UV- blocking properties in the wider wavelength range of 259-322nm(4.80eV-3.850eV). The PMMA nanocomposites with 2.0 wt% CH3NH3PbBr3:WO3 filler composition exhibited highest UV-shielding behavior with maximum UV-absorption in the wavelength range of 260 to 300nm. The pristine PMMA films showed a PL emission peak at 410nm while the PMMA nanocomposites exhibited strong emissions in the wavelength range of 485-520nm. The observed hydrophobicity, redshift and longer lifetime decay of 34.3 ns for PMMA nanocomposites is attributed to the incorporated CH3NH3PbBr3:WO3 heterojunction nanoparticles. The chromaticity profile suggested that the emission color changed from blue to green as the filler dose of CH3NH3PbBr3:WO3 varied from 0 to 2.0 wt%. Additionally, the findings from the study reveal that incorporation of CH3NH3PbBr3:WO3 into the PMMA matrix enhances UV-absorption, optical conductivity, hydrophobicity, thermal stability, electrical conductivity and photon-down conversion properties of PMMA which make the material suitable for photonic, photovoltaic, optoelectronic and light emitting diode applications.

Development of polyvinyl alcohol/carboxymethylcellulose-based bio-packaging film with citric acid crosslinking and clove essential oil encapsulated chitosan nanoparticle pickering emulsion

This study developed polyvinyl alcohol (PVA)/carboxymethylcellulose (CMC)-based films, using citric acid (CA) as a non-toxic crosslinking agent, to enhance the shelf life of water-soluble packaging films. Clove essential oil (CEO)-loaded chitosan nanoparticles (CSNPs) were prepared via Pickering emulsion and incorporated into PVA/CMC/CA composite films. The encapsulation of CEO was confirmed by FTIR and optical microscopy. Thermal properties were analyzed using thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC), revealing improved thermal stability and a decrease in glass transition temperature (Tg) upon crosslinking. The formation of ester bonds was confirmed by ATR-FTIR and 13CNMR. Water contact angle (WCA) measurements showed a decrease in hydrophilicity, enhancing the barrier properties of the films. SEM images demonstrated good dispersion of CSNP/CEO within the matrix, improving mechanical and barrier properties. The films exhibited a 30 % reduction in water vapor permeability and water solubility. Controlled release studies indicated that the composite films sustained CEO release, extending the shelf life of cherry tomatoes. Thus, these PVA/CMC/CA-CSNP/CEO composite films offer strong potential for food preservation applications.

3D printing of biodegradable biocomposites based on forest industrial residues by fused deposition modeling

This study investigated the impact of industrial forest residues (IFR) type and proportion on 3D-printed biocomposites (BC). Fused deposition modeling (FDM) produced BC containing up to 20 % Jack pine sawdust, wood ashes, cellulose fibers, and polylactic acid (PLA). The BC thermal stability, surface chemistry, microstructure, and physical and mechanical were investigated. Thermal stability investigations revealed that adding IRF resulted in a decline in the PLA degradation temperature, an increase in the residual mass, a decrease in the glass transition temperature, and an improvement in crystallinity. Add IRF to PLA showed an important reduction in ductility, a consistent reduction of the tensile and flexural strengths with increasing proportion but only a slight or a non-significant reduction the modulus of elasticity. Adding forest waste filler to pure PLA increased the water absorption (WA) and dimensional accuracy (TA) of the biocomposites, which was expected due to the hydrophilic character of fillers. The microstructural analysis demonstrated that a higher filler level resulted in a greater porosity, roughness, and visible filler pull-out on the filament and printed parts surfaces. Surface chemistry analysis suggested poor interactions between the PLA and the fillers and consequently poor interfacial adhesion. Furthermore, the rheological investigations confirmed that the complex viscosity and storage modulus of PLA-Jack pine's sawdust and PLA-cellulose fibers increased with filler. In contrast, the PLA-wood ashes showed opposite results. Using 3D-printed biodegradable biocomposites provided a sustainable option for reducing dependence on non-renewable plastic, valorizing the value chain of forest products, and promoting the circular economy.

Fabrication of gallic acid containing poly(vinyl alcohol)/chitosan electrospun nanofibers with antioxidant and drug delivery properties

Chitosan-based nanofibers with excellent properties are attractive materials for specific industrial applications of contemporary interest. This work aims to fabricate functional nanofibers based on poly(vinyl alcohol)/chitosan (CS) with an antioxidant and model drug molecule, gallic acid (GA), by electrospinning, followed by cross-linking through glutaraldehyde (PVA-CS-GAs). PVA-CS-GAs were electrospun at two different concentrations by the adjustment of the CS feeding ratio. The detailed characteristics of the as-prepared electrospun nanofibers were elucidated by Fourier Transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), water contact angle (WCA) measurements, thermogravimetric and differential scanning calorimetry (TGA and DSC) analyses. SEM images indicated that the average fiber diameter distribution was in the range of 90–110 nm. The results show that morphology, mean diameter, wettability, and thermal characteristics of the composite nanofibers were affected by the CS feeding ratio. Although the increase in the amount of polar -OH groups with the addition of GA caused an improvement in the hydrophilicity and thermal stability of the electrospun nanofibers, it also caused a decrease in the thermal transition temperatures. Furthermore, antioxidant tests based on DPPH radical scavenging ability and in vitro release studies demonstrated that the cross-linked PVA-CS-GA composite nanofibers have good antioxidant activity and a pH-dependent drug release rate, indicating their potential for implementation in wound healing and drug delivery applications.

Mechanisms of electrical transition using a conformal MoOx cap on Mo-doped VO2 thermochromics

Mo-doped VO2 thin-films are deposited on the soda-lime glass by a reactive high-power impulse magnetron co-sputtering technique (R-HiPIMS). Rapid thermal annealing at 500 °C for 3 min is performed to achieve the fabrication under low thermal budget. To prevent VO2 from further oxidation, a conformal and semi-conducting MoOx film is applied as the capping layer by the plasma-enhanced atomic layer deposition (PE-ALD). After MoOx film is deposited, an electrical transition in the resistance ratio of 6–10 orders of magnitude has been found, especially for MoOx thicknesses less than 20 nm. A secondary phase of V2O3 plays an important role in abrupt change of current transportation. Also, the hysteresis of optical transition in transmittance at a wavelength of 2500 nm shows that both the width and transition temperature (TC) decrease with increasing the thickness of the MoOx cap. Moreover, the effect of localized surface plasmonic resonance (LSPR) due to the Karst-like structure has been detected by the absorption spectrum. The variations in LSPR peak, such as intensity, blue-shifting, and red-shifting, originated from either excess carrier or structure change are discussed. The high aspect ratio of surface morphology is further examined by atomic force microscopy. In addition, the coverage of MoOx on Mo-doped VO2 concerning the friction behavior is evaluated by lateral force microscopy (LFM), which is helpful in clarifying the responsible mechanisms during TC transition.

Influence of polar‐modified ESBO on the thermal and mechanical properties of FKM/EPDM rubber blends

AbstractRenowned for its oil, heat, and chemical resistance, fluoroelastomer rubber (FKM) also presents notable drawbacks, such as inferior low‐temperature performance. In this study, 2,2‐trifluoroethylamine (TF) and 2,4‐difluorobenzylamine (DF) were grafted onto epoxidized soybean oil (ESBO) to generate two innovative plasticizers: ESBO‐TF and ESBO‐DF that they were specifically designed to augment the low‐temperature performance of FKM. A thorough investigation into the effects of ESBO‐TF/DF on FKM/EPDM blends' properties was conducted. The study demonstrated that the integration of ESBO‐TF and ESBO‐DF enhanced the vital properties of the FKM/EPDM blends, including elongation at break, tear strength, and, significantly, low‐temperature performance. There was a noticeable decrease in the glass transition temperature (Tg), dropping by 3.54 and 2.95°C with the incorporation of 10 phr ESBO‐TF and ESBO‐DF, respectively. These respective plasticizers showed positive effects on the plasticization and compatibilization of the FKM/EPDM blends, thus proposing a novel methodology for developing new plasticizers for FKM and related blends.

Inverse magnetic catalysis and energy loss in a holographic QCD model

In this paper, we consider the Einstein-Maxwell-dilaton holographic model for light quarks with nonzero magnetic field and chemical potential. First, we study the phase diagrams in T−μ and T−B planes. We observe inverse magnetic catalysis which is consistent with the lattice QCD results. We discuss the influence of the magnetic field and chemical potential on the location of the critical end point (CEP). It is found that the magnetic field increases the critical μCEP of the CEP in the T−μ plane and the chemical potential increases the critical BCEP of the CEP in the T−B plane. Second, we discuss the equations of state (EOS) with nonzero magnetic field and chemical potential. We observe that the EOS near the phase transition temperature are nonmonotonic. Then we study the energy loss with a nonzero magnetic field and chemical potential. It is found that the drag force of the heavy quark and jet quenching parameter q^ show an enhancement near the phase transition temperature. The peak values of drag force and q^ are pushed toward lower temperature with increasing B or μ. This phenomenon is consistent with the phase transition temperature decrease with increasing B or μ in this holographic model. Moreover, we find that the heavy quark may lose more energy when it is perpendicular to a magnetic field, which is consistent with the results of the jet quenching parameter. Published by the American Physical Society 2024

Exploring the impact of CuCl2 modification on structural variations and dielectric constant in bismuth borate tellurite glasses

Copper chloride doped boro-tellurite-based glass series with compositions 60TeO2-(25-x) Bi2O3–15B2O3-xCuCl2 (x = 0, 5, 10, 15, and 20) were synthesized using the traditional melt-quench procedure. The X-ray diffraction patterns of the examined glasses reveal their amorphous nature. The effect of CuCl2 addition on the glass network/structural units was studied using vibrational (FTIR/Raman) spectroscopy, and CuCl2 inclusion in the glass matrix resulted in a transformation from compact TeO4 to TeO3 structural units This shows that copper chloride acts as a modifier in the examined glass series, resulting in the creation of non-bridging oxygen (NBOs), meaning that the loosening of the glass network is further supported by a decrease in the glass transition temperature as CuCl2 content increases. UV–Vis DRS spectra of examined glasses reveal an absorption band corresponding to the typical transition of Cu2+ ions from 2B1g → 2B2g, situated in deformed octahedral sites in absorption spectra. As Cu+ concentration rises, the indirect optical band gap values drop from 2.94 eV to 1.75 eV. The metallization criterion values lie between 0.383 and 0.300 suggesting that these glasses are potential candidates for nonlinear optical applications. With an increase in Cu+ concentration, the values of molar refractive index (Rm) and molar electronic polarizability αm increases from 22.412 to 26.205 and 8.894 to 10.398 respectively, which correlate with increasing dielectric constant (ε′) values as the Cu+ amount increases. Further dielectric studies reveal non-Debye-type relaxation behaviour.

Empirical model for the effect of air humidity during manufacturing on the glass transition temperature of carbon fiber reinforced hot curing epoxy – a case study

Carbon fiber-epoxy laminates are used in aerospace manufacturing, e.g. as substrates for solar cells of satellites. Commonly, fibers or fibermats are impregnated with epoxy resin and placed in the required orientation. During subsequent curing, the resin molecules are crosslinked. Cured parts are characterized by their glass transition temperature (Tg). It has been observed that Tg of epoxy matrix resin vary with recorded absolute air humidity during wet fiber placement manufacturing. Based on the production data of a series production of 203 carbon fiber laminates for space application, an empirical linear relationship between the absolute air humidity at the beginning of each production day and the observed glass transition temperature of the fully cured laminate is formulated and validated. The empirical equation describes a linear decrease of achievable glass transition temperature with increasing absolute air humidity. The quantitative nature of the results encourages straightforward practical application to determine the maximum achievable Tg for given production conditions.

Ionic conductivity and dielectric characteristics of a Li incorporated PVA electrolyte membrane and a study of a fully solid-state electrochromic device based on it

The construction and study of a fully solid state electrochromic (EC) device with cathodic coloration exhibiting very fast response times (< 1s) is reported using a WO3 EC layer and a poly (vinyl alcohol) (PVA)- Lithium acetate membrane electrolyte. Broadband dielectric studies on the polymer membranes with different Li concentrations show multiple relaxation mechanisms out of which a segmental relaxation prominent beyond a certain composition is strongly correlated with Li-ion conduction yielding better ionic conductivity and reversible coloration in the EC device. The relatively high Li conductivity in PVA has a direct correspondence with the lowering of the crystallinity of PVA and a decrease of the glass transition temperature, Tg with increasing Li addition. A simple model of the coloration process suggests that the short electrolyte diffusion length coupled with a high electric field and an interfacial emf that varies as ≈t−0.6 results in the swift current response of the film with an optimal performance at 20 wt.% Li in PVA, exceeding which irreversible coloration can occur on the surface. The transient current is crucial for the observed swift switching characteristics. Ageing studies for almost a month indicate potential stability of the EC device for over 150 cycles.

Tuning the Mechanical Properties of 3D-Printed Objects by Mixing Chain Transfer Agents in Norrish Type I Photoinitiated RAFT Polymerization.

Photoinduced 3D printing via photocontrolled reversible-deactivation radical polymerization (photoRDRP) techniques has emerged as a robust technique for creating polymeric materials. However, methods for precisely adjusting the mechanical properties of these materials remain limited. In this study, we present a facile approach for adjusting the mechanical properties of 3D-printed objects by adjusting the polymer dispersity within a Norrish type I photoinitiated reversible addition-fragmentation chain transfer (NTI-RAFT) polymerization-based 3D printing process. We investigated the effects of varying the concentrations and molar ratios of trithiocarbonate (BTPA) and xanthate (EXEP) on the mechanical properties of the printed materials. Our findings demonstrate that increased concentrations of RAFT agents or higher proportions of the more active BTPA lead to a decrease in Young's modulus and glass transition temperatures, along with an increase in elongation at break, which can be attributed to the enhanced homogeneity of the polymer network. Using a commercial LCD printer, the NTI-RAFT-based 3D printing system effectively produced materials with tailored mechanical properties, highlighting its potential for practical applications.

Hygrothermal aging mechanism of epoxy composites used for medium-frequency transformers

The integration of medium-frequency transformer design and the harsh service environment raise higher demands for the medium-frequency insulation performance of epoxy composites. As epoxy composite's frequency response characteristics and sensitivity to moisture intrusion are still unknown, its application as the insulation materials of medium-frequency transformers under hygrothermal conditions is limited. This paper investigates the mechanism of moisture intrusion damage to the molecular structure of the epoxy resin matrix and its cross-linking points with the curing agent. The regularity of medium-frequency insulation performance degradation of epoxy composites after hygrothermal aging is studied. Results indicate that after 40 days of hygrothermal aging, moisture together with high temperature damaged the main chain of the epoxy resin and its cross-linking points with the curing agent, resulting in a 23 °C decrease in the glass transition temperature and an 82 % decrease in cross-linking density of the epoxy composite. Moisture ionization and the increase of carriers due to epoxy resin hydrolysis lead to an increase in the amount of space charge. The temperature rise caused by dipole steering polarization facilitates the formation of internal conductive pathways in the epoxy composite, resulting in a 73 % decrease in the medium-frequency breakdown strength and a four-order magnitude decrease in the medium-frequency volume resistivity of the epoxy composite. This study can guide the insulation design of high-reliability medium-frequency transformers.

Exploring the Impact of Bio-Based Plasticizers on the Curing Behavior and Material Properties of a Simplified Tire-Tread Compound.

The tire industry needs to become more sustainable to reduce pollution and fight climate change. Replacing fossil ingredients in a tire-tread compound with bio-based alternatives is an approach to create a more sustainable product. For instance, the plasticizer can be replaced, which is a petroleum-based ingredient used in relatively high amounts in the rubber. This approach was followed in the current study. Three plant-based plasticizers were selected as potential substitutes for treated distillate aromatic extract (TDAE) in a simplified tire-tread compound formulation, namely, sunflower oil, coconut oil, and cardanol. Additionally, squalane was used as a TDAE replacement to further investigate the possible interactions between plasticizers and other compound ingredients. Squalane (C30H62) is a fully saturated substance, containing six methyl groups but no additional chemical functional groups. Therefore, it was expected that squalane would result in limited interactions within the studied system. All alternatives to TDAE showed an increased cure rate and decreased scorch time, except squalane. This indicates that the three bio-based plasticizers might interact with the vulcanization system. For example, they could function as an additional coactivator of the curing system and/or shield the silica surface. A severe decrease in maximum torque and an increase in elongation at break were obtained for cardanol and sunflower oil. Both plasticizers also resulted in lower crosslink densities compared to the other compounds. A model study with the bio-plasticizers and sulfur verified that the unsaturation in the cardanol and sunflower oil reacted with the crosslinking agent. This leads to less sulfur available for the curing reaction, explaining the low maximum torque. The tan δ curves showed that all replacements resulted in a decrease in the glass transition temperature of the compound. Although all oil alternatives displayed promising results, none of them are suitable as a direct substitute for TDAE in a tire-tread compound due to its ability to interact additionally with other rubber ingredients and contribute in this form to the reinforcement of the compound.

Studies on the compositional dependent structural and electrical properties of CaTiO3-modified K0.5Na0.5NbO3 piezoelectric system

Lead-free piezoelectric ceramics of (1 − x)K0.5Na0.5NbO3-xCaTiO3 were fabricated, and their crystal structure, microstructure, and electrical properties were systematically studied. Rietveld refinement of the x-ray diffraction data and Raman spectroscopic analyses revealed a composition-dependent structural phase transition: three phase transitions, namely, from a pure orthorhombic phase for x ≤ 0.02 to a mixed phase of orthorhombic and tetragonal phases (0.03 ≤ x ≤ 0.08) and finally another mixed phase of tetragonal + cubic for x = 0.10 and 0.15 at room temperature (RT). The morphological study reveals a decrease in grain size along with a more uniform distribution of grains as the concentration of CaTiO3 (CT) increases; notably, a homogeneous distribution of grains is observed for x = 0.05. The temperature-dependent dielectric properties show two phase transitions, from orthorhombic to tetragonal (TO-T) and tetragonal to cubic (TC), for unmodified K0.5Na0.5NbO3 (KNN). However, both the phase transition temperatures (TO-T and TC) decrease, and the transition peaks broaden with an increase in CT substitution, and for x &amp;gt; 0.06, the TO-T shifted below RT. The broadening of the transition peak at TO-T may be due to the relaxation behavior. Among the prepared samples, the 5 mol. % CT-modified KNN shows the optimum electrical properties (d33 = 114 pC/N, ɛr = 412, and 2Pr = 15.25 μC/cm2) at RT. The enhanced electrical properties for x = 0.05 are due to the coexistence of orthorhombic and tetragonal phases, facilitating easy polarization rotation and flattening of the free energy profile. A phase diagram has been constructed based on the information gathered from the temperature-dependent dielectric measurements, RT x-ray diffraction, and Raman spectroscopy data and is discussed in detail.

Effect of cobalt doping on the structural, magnetic, optical, and electronic properties of LiFeCr4O8

Cobalt doping's influence on the structural, magnetic, and electronic properties of the double spinel LiFeCr4O8 was systematically investigated. Rietveld refinement revealed a consistent increase in lattice parameter a and unit cell volume with cobalt incorporation. Magnetic susceptibility measurements indicated three distinct transitions: an increase in the ferrimagnetic transition temperature (TN), a decrease in the magnetostructural transition temperature (TMS), and an increase in the spin gap transition by cobalt doping. Through diffuse reflectance spectroscopy the direct optical band gap (Eog) was obtained with values of 1.169 eV, 1.303 eV, 1.396 eV, and 1.230 eV for x = 0.0, 0.1, 0.2, and 0.5, respectively. The observed increase in Eog with cobalt doping suggests a widening of the band gap, which could be beneficial for optoelectronic applications. By means of X-ray photoelectron spectroscopy (XPS) the core levels of Li 1s, Co 3p, Fe 3p, Cr 3p, Fe 2p, Cr 2p, and O 1s were identified. XPS valence band (VB) analysis revealed a decreasing intensity at binding energy BE = 0 eV with respect to x = 0.0. Density functional theory calculations with Hubbard U correction (DFT + U) confirmed a ferrimagnetic semiconductor behavior with a direct electronic band gap (Eeg) of 1.085 eV.

Preparation and Properties of PA10T/PPO Blends Compatibilized with SEBS-g-MAH.

Plant-derived PA10T is regarded as one of the most promising semi-aromatic polyamides; however, shortcomings, including low dimensional accuracy, high moisture absorption, and relatively high dielectric constant and loss, have impeded its extensive utilization. Polymer blending is a versatile and cost-effective method to fabricate new polymeric materials with excellent comprehensive performance. In this study, various ratios of PA10T/PPO blends were fabricated via melt blending with the addition of a SEBS-g-MAH compatibilizer. Molau test and scanning electron microscopy (SEM) were employed to study the influence of SEBS-g-MAH on the compatibility of PA10T and PPO. These studies indicated that SEBS-g-MAH effectively refines the domain size of the dispersed PPO phase and improves the dispersion stability of PPO particles within a hexafluoroisopropanol solvent. This result was attributed to the in situ formation of the SEBS-g-PA10T copolymer, which serves as a compatibilizer. Differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA) results showed that the melting-crystallization behavior and thermal stability of blends closely resembled that of pure PA10T. Dynamic mechanical analysis (DMA) revealed that as the PPO content increased, there was a decrease in the glass transition temperature and storage modulus of PA10T. The water absorption rate, injection molding shrinkage, dielectric properties, and mechanical strength of blends were also systematically investigated. As the PPO content increased from 10% to 40%, the dielectric loss at 2.5 GHz decreased significantly from 0.00866 to 0.00572, while the notched Izod impact strength increased from 7.9 kJ/m2 to 13.7 kJ/m2.

Structural phase transitions in multicomponent La0.2Nd0.2Sm0.2Gd0.2RE50.2NbO4 (RE5 = Ho, Y, Tb, Eu, Pr) oxides

AbstractIn this work, the influence of compositional complexity on the structural and thermal properties of multicomponent rare‐earth ortho‐niobates from the La0.2Nd0.2Sm0.2Gd0.2RE50.2NbO4 (RE5 = Ho, Y, Tb, Eu, Pr) series was investigated. Based on X‐ray powder diffraction studies using synchrotron radiation, it was found that all tested materials were pure single‐phase compositions and showed stability in the monoclinic I2/c crystal structure at room temperature. High‐temperature X‐ray powder diffraction studies and dilatometry studies confirmed the presence of a structural phase transition between low‐temperature (I2/c) and high‐temperature (I41/a) polymorphs. The structural phase transition temperatures are between 676°C and 701°C. Interestingly, despite their compositional complexity, the structural phase transition temperature behaves similarly to conventional ortho‐niobates, that is, it depends on the radius of the A‐cation; that is, as the ionic radius increases, the phase transition temperature decreases. The transition has been categorized as a second‐order phase transition based on the observed relationship between the Landau order parameter and spontaneous strain. The coexistence of the tetragonal and monoclinic phases has been seen in all compositions around the temperature of the structural phase transition. The presence of two orientation states in the monoclinic structure leads to the so‐called spontaneous strain, which consists of longitudinal (u) and shear (v) strain components. The values of these strains at 300°C range between 2.42 and 2.58 × 10−2 for longitudinal, 2.98 and 3.04 × 10−2 for shear, and 5.46 and 5.57 × 10−2 for scalar spontaneous strain. It was found that the spontaneous strain in each of the materials under test was very little impacted by the variation in the complexity of the A sublattice's composition. In addition, thermal expansion coefficients of both polymorphs were determined, which range from 12.7 × 10−6 K−1 to 13.2 × 10−6 K−1 for the monoclinic structure and 9.7 × 10−6 K−1 to 9.9 × 10−6 K−1 for the tetragonal one.