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The removal of pharmaceutical contaminants from wastewater has gained considerable attention in recent years, particularly in the advancements of hydrogel-based adsorbents as a green solution for their ease of use, ease of modification, biodegradability, non-toxicity, environmental friendliness, and cost-effectiveness. This study focuses on the design of an efficient adsorbent hydrogel based on 1% chitosan, 40% polyethylene glycol 4000 (PEG4000), and 4% xanthan gum (referred to as CPX) for the removal of diclofenac sodium (DCF) from water. The interaction between positively charged chitosan and negatively charged xanthan gum and PEG4000 leads to strengthening of the hydrogel structure. The obtained CPX hydrogel, prepared by a green, simple, easy, low-cost, and ecological method, has a higher viscosity due to the three-dimensional polymer network and mechanical stability. The physical, chemical, rheological, and pharmacotechnical parameters of the synthesized hydrogel were determined. Swelling analysis demonstrated that the new synthetized hydrogel is not pH-dependent. The obtained adsorbent hydrogel reached the adsorption capacity (172.41 mg/g) at the highest adsorbent amount (200 mg) after 350 min. In addition, the adsorption kinetics were calculated using a pseudo first-order model and Langmuir and Freundlich isotherm parameters. The results demonstrate that CPX hydrogel can be used as an efficient option to remove DCF as a pharmaceutical contaminant from wastewater.

The tin-doped TiO2 powders obtained by sol-gel and microwave-assisted sol-gel methods were investigated. The synthesis took place in a basic medium (pH 10, ammonium hydroxide, 25%) starting from tetrabutyl orthotitanate in its parental alcohol. In the case of the dopant, Tin(II) 2-ethylhexanoate as SnO2 precursor was used in the amount of 1, 2, or 4 mol % SnO2. Based on thermal analysis data, the powders were thermally treated in air, at 500 °C. The comparative investigation of the structure and morphology of the nanopowders annealed at 500 °C was performed by scanning electron microscopy (SEM), high-resolution transmission electron microscopy with selected area electron diffraction (HRTEM/SAED), scanning transmission electron microscopy (STEM) coupled with EDX mapping, Fourier transmission infrared (FTIR), UV–Vis, Raman and photoluminescence (PL) spectroscopy, X-ray diffraction (XRD), and X-ray florescence spectroscopy (XRF). The obtained materials were tested for the photocatalytic removal of methyl orange dye from aqueous solutions. High degradation efficiencies (around 90%) were obtained by Sn doping after 3 h of UV light irradiation.

Bacterial cellulose (BC) is a biopolymer whose properties have been intensively studied, especially for biomedical applications. Since BC has no antimicrobial activity, it is necessary to use bioactive substances for developing wound healing applications. Another drawback of BC is the loss if its water retention capacity after dehydration. In order to overcome these problems, carboxymethyl cellulose (CMC) and turmeric extract (TE) were selected for the preparation of BC composites. Citric acid (CA) was used as the crosslinking agent. These composites were tested as potential antimicrobial wound dressing materials. TE-loaded BC–CMC composites were characterized in terms of their morphology, crystallinity, and thermal behavior. Swelling tests and curcumin-release kinetic analysis were also performed. All the composites tested had high swelling degrees, which is an advantage for the exudate adsorption from chronic wounds. The antibacterial potential of such composites was tested against Escherichia coli (E. coli), Staphylococcus aureus (S. aureus), and Candida albicans (C. albicans). The in vitro cytotoxicity toward L929 fibroblast cells was studied as well. The obtained results allow us to recommend these composites as good candidates for wound dressing applications.

In this paper, the thermal decomposition of crystalline Al(OH)3 was studied over the temperature range of 260–400 °C for particles with a size between 10 and 150 µm. The weight losses and thermal effects occurring in each of the dehydration process were assessed using thermogravimetry (TG) and differential scanning calorimetry (DSC) thermal analysis. X-ray diffraction (XRD) patterns, refined by the Rietveld method, were used for mineral phase identification, phase composition analysis, and crystallinity degree determination. Moreover, the particle size distributions and their corresponding D10, D50, and D90 numeric values were determined with a laser analyzer. We observed a strong relationship between the calcination temperature, the initial gibbsite grade particle size, and the crystallinity of the resulting powders. Hence, for all endothermic effects identified by DSC, the associated temperature values significantly decreased insofar as the particle dimensions decreased. When the gibbsite was calcined at a low temperature, we identified small amounts of boehmite phase along with amorphous new phases and unconverted gibbsite, while the powders calcined at 400 °C gradually yielded a mixture of boehmite and crystalized γ-Al2O3. The crystallinity % of all phase transition products declined with the increase in particle size or temperature for all the samples.

In this study, two types of mesoporous silica with different pore structures and volumes were synthesized by the soft-templating method. The two types of mesoporous silica, type MCM-41 and MCM-48, were loaded with three polyphenols—caffeic acid, p-coumaric acid and trans-ferulic acid—in the same ratio of mesoporous silica:polyphenol (1:0.4 w/w). The materials obtained were characterized from a morphological and structural point of view through different analysis techniques. Through X-ray diffraction (XRD), the crystallization plane and the ordered structure of the mesoporous silica were observed. The difference between the two types of materials containing MCM-41 and MCM-48 was observed through the different morphologies of the silica particles through scanning electron microscopy (SEM) and also through the Brunauer–Emmet–Teller (BET) analysis, that the surface areas and volumes of pores was different between the two types of mesoporous silica, and, after loading with polyphenols, the values were reduced. The characteristic bands of silica and of polyphenols were easily observed by Fourier-transform infrared spectroscopy (FTIR), and, through thermogravimetric analysis (TGA), the residual mass was determined and the estimated amount of polyphenol in the materials and the efficient loading of mesoporous silica with polyphenols could be determined. The in vitro study was performed in two types of simulated biological fluids with different pH—simulated gastric fluid (SGF) and simulated intestinal fluid (SIF). The obtained materials could be used in various biomedical applications as systems with controlled release of natural polyphenols and the most suitable application could be as food supplements especially when a mixture of such materials is used or when the polyphenols are co-loaded within the mesoporous silica.

Tailoring electrical and mechanical properties in the fluorite oxides family is of great interest for technological applications. Other than doping and substitution, entropy-driven stabilization is an emerging technique for new solid solutions formation and enhancing or exploring new functionalities. However, there is a high number of possible combinations for higher-order diagram investigations, and the current state of the art shows limited possibilities in predicting phase formation and related properties. In this paper, we expand the compositional space of fluorite oxides in ZrO2-HfO2-CeO2-Nb2O5-RE2O3 systems. X-ray diffractometry and scanning electron microscopy measurements showed the formation of cubic fluorite-type structures when processing compositions at 1600 °C.

Graded structures with different architectures were obtained by spark plasma sintering from (Ba1-xSrx)TiO3 (BST, x = 0.10; 0.20; 0.30) powders. The presence of the composition gradient was confirmed by structural and compositional investigations using X-ray diffraction and electron microscopy combined with energy dispersive X-ray spectroscopy. The concentration gradient was either asymmetric (3 layers, starting with x = 0.10 and ending with x = 0.30) or symmetric (5 or 6 layers, starting and ending with x = 0.10, and with a single or double x = 0.30 layer in the middle, respectively). Electrical measurements reveal a decrease of the dielectric constant with increasing the number of the layers. It was found that the symmetric graded structure with 6 layers has the best thermal stability of both, the dielectric constant (variation of only 8% between zero and 100 °C) and the pyroelectric coefficient (6% variation between zero and 80 °C). In addition, an enhancement of the pyroelectric signal for frequencies above 100 Hz is obtained in symmetric structures, an effect that is attributed to the additive contributions of the signals originated from the layers with different Sr content.

This paper introduces for the first time the preparation of cobalt aluminate (CoAl2O4) nanoparticles through a solution combustion method using a Mentha piperita leaves extract. The active constituents present in the mentha leaves extract act as both a chelating and a reducing agent. The isolated precursor was characterized by FTIR, UV–Vis, thermal analysis and XPS. Various techniques (XRD, SEM and TEM, XPS, FTIR and UV–Vis) were also used to characterize the cobalt aluminate spinel from the point of view of structure, morphology and surface chemistry. XRD confirmed the formation of a single-phase, crystalline cubic spinel structure with mean crystalline domain size of 19.5 nm. The TEM analysis showed rhombic and rectangular CoAl2O4 nanoparticles with unimodal particle size distribution and average particle size of about 35 nm. The characteristic peaks of the CoAl2O4 spinel were highlighted by the FTIR spectrum. The tetrahedral configuration of Co2+ ions in the CoAl2O4 spinel structure was illustrated by the absorbance and XPS spectra. Furthermore, XPS spectra reveal both tetrahedral and octahedral configurations of Al3+ ions. To evaluate the catalytic properties of the cobalt aluminate, the photocatalytic degradation of methylene blue (MB) was carried out under visible light irradiation.

The main objective of the study was to produce alternative binder materials, obtained with low cost, low energy consumption, and low CO2 production, by regenerating end-of-life (EOL) materials from mineral deposits, to replace ordinary Portland cement (OPC). The materials analyzed were ash and slag from the Turceni thermal power plant deposit, Romania. These were initially examined for morphology, mineralogical composition, elemental composition, degree of crystallinity, and heating behavior, to determine their ability to be used as a potential source of supplementary cementitious materials (SCM) and to establish the activation and transformation temperature in the SCM. The in-situ pozzolanic behavior of commercial cement, as well as cement mixtures with different percentages of ash addition, were further observed. The mechanical resistance, water absorption, sorptivity capacity, resistance to alkali reactions (ASR), corrosion resistance, and resistance to reaction with sulfates were evaluated in this study using low-vacuum scanning electron microscopy.

Four different functional properties at room temperature were found in Ba12Fe28Ti15O84 quaternary ferrite ceramics: a thermoelectric character with a prominent Seebeck coefficient of -400 μV/K, a strong ferrimagnetic character and weak magnetoresistivity, non-linear dielectric character (tunability) and ferro/piezoelectric response. The complex crystalline structure with a naturally occurring self-organized layered structure was mapped by High Resolution Transmission Electron Microscopy. A n-type conduction was found for optimized samples, consistent with the negative Seebeck coefficient. The presence of magnetic domains with a lateral size ranging from few hundreds of nanometers, up to few microns, extended over several grains indicates a strong intergranular magnetic interaction. Local ferroelectric switching as revealed by piezoresponse force microscopy showed a relatively weak effective piezoelectric coefficient with a remnant value of 0.5 p.m./V and a clockwise cycling direction, which was attributed to an effective negative piezoelectric coefficient. The switching behavior was described as originating from the material’s nanoscale layered complexity, with a strong anisotropy of its dielectric and ferro/piezoelectric local properties.

This paper aims to improve medical strategies regarding cancer treatment, by developing new targeted cancer therapy nanostructured systems, based on magnetite and natural catabolism products as coating agents (glutamic acid, tartaric acid), with induced cellular internalization. In order to create hydrophilic, biocompatible systems, suitable for targeted cancer therapy, and minimize the negative side effects of current approaches, a one-pot synthesis by co-precipitation technique, starting from Fe2+ and Fe3+ inorganic precursors and multifunctional organic compounds, carefully controlling the reaction parameters (concentration of precursors, pH, temperature etc.) was performed. The obtained Fe3O4 stabilised nanoparticles were subjected to morphological and structural characterization. The formation of inorganic-organic hybrid systems was evaluated using FTIR spectroscopy and complex thermal analysis (TG / DSC) for determining the content of the organic component, while X-ray Diffractometry and Scanning and Transmission Electron Microscopy were used to characterize the crystallinity and particle dimensions and distribution. The magnetic properties at room temperature were also evaluated, recording the magnetic susceptibility relative to the applied magnetic field.

Single-phase Ba1-xSrxTiO3 (BST) perovskite ceramics with 0.3 ≤ x ≤ 0.4 were prepared from powders synthesized via sol-gel route. The compositions have the ferroelectric-paraelectric phase transition close to room temperature. At 20 °C the BST ceramics are ferroelectric for 0.3 ≤ x ≤ 0.35 and paraelectric for x = 0.375 and x = 0.40. The study follows the relation between the structural changes produced when increasing the Sr content and the dielectric properties at low intensity electric fields. It is found that the grain size and tetragonality decreases as the Sr content increases. Analyses of complex permittivity and impedance spectroscopy reveal the temperature and frequency dependencies of the dielectric properties. The phase transitions seem to be of first order for all compositions, with a thermal hysteresis that decreases with increasing the Sr content, fact attributed to the corresponding increase of the grain boundaries weight allowing a more efficient stress relaxation in the structure during the change of the symmetry from cubic to tetragonal. The diffusiveness degree during the phase transition is increasing with Sr content, suggesting some relaxor-type contribution attributed to smaller grain size. The ac conductivity follows the universal Jonscher law, with an ac component having the power parameter s independent of Sr content, and a dc component that it is thermally activated with an activation energy of about 0.7–0.77 eV attributed to oxygen vacancies acting as donor-like defects. The fit of impedance spectra at different temperatures and frequencies is obtained by using an equivalent circuit accounting the grains, grain boundaries, electrode interfaces and the local contributions produced by reorientation of defect dipoles or defect clusters. All the component circuits have significant variations around phase transitions. These are discussed in relation to structural changes occurring during transition and considering the changes in the distribution of various charges when polarization vanishes.

The present research focuses on the physicochemical and pharmacotechnical properties of new hydrogels obtained using allantoin, xanthan gum, salicylic acid and different concentrations of Aloe vera (5, 10, 20% w/v in solution; 38, 56, 71 wt% in dry gels). The thermal behavior of Aloe vera composite hydrogels was studied using DSC and TG/DTG analyses. The chemical structure was investigated using different characterization methods (XRD, FTIR and Raman spectroscopies) and the morphology of the hydrogels was studied SEM and AFM microscopy. Pharmacotechnical evaluation on tensile strength and elongation, moisture content, swelling and spreadability was also completed. Physical evaluation confirmed that the appearance of the prepared Aloe vera based hydrogels was homogeneous and the color varied from pale beige to deep opaque beige with increasing Aloe vera concentration. All other evaluation parameters, e.g., pH, viscosity, spreadability and consistency were found to be adequate in all hydrogel formulations. SEM and AFM images show that the structure of the hydrogels condensed into homogeneous polymeric solids with the addition of Aloe vera, in accordance with the decrease in peak intensities observed via XRD analysis. These results suggest interactions between the hydrogel matrix and Aloe vera as observed via FTIR and TG/DTG and DSC analyses. Considering that Aloe vera content higher than 10% (w/v) did not stimulate further interactions, this formulation (FA-10) can be used for further biomedical applications.

This research focused on the synthesis of apatite, starting from a natural biogenic calcium source (egg-shells) and its chemical and morpho-structural characterization in comparison with two commercial xenografts used as a bone substitute in dentistry. The synthesis route for the hydroxyapatite powder was the microwave-assisted hydrothermal technique, starting from annealed egg-shells as the precursor for lime and di-base ammonium phosphate as the phosphate precursor. The powders were characterized by Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray analysis (EDAX), transmission electron microscopy (TEM), X-ray fluorescence spectroscopy (XRF), and cytotoxicity assay in contact with amniotic fluid stem cell (AFSC) cultures. Compositional and structural similarities or differences between the powder synthesized from egg-shells (HA1) and the two commercial xenograft powders—Bio-Oss®, totally deproteinized cortical bovine bone, and Gen-Os®, partially deproteinized porcine bone—were revealed. The HA1 specimen presented a single mineral phase as polycrystalline apatite with a high crystallinity (Xc 0.92), a crystallite size of 43.73 nm, preferential growth under the c axes (002) direction, where it mineralizes in bone, a nano-rod particle morphology, and average lengths up to 77.29 nm and diameters up to 21.74 nm. The surface of the HA1 nanoparticles and internal mesopores (mean size of 3.3 ± 1.6 nm), acquired from high-pressure hydrothermal maturation, along with the precursor’s nature, could be responsible for the improved biocompatibility, biomolecule adhesion, and osteoconductive abilities in bone substitute applications. The cytotoxicity assay showed a better AFSC cell viability for HA1 powder than the commercial xenografts did, similar oxidative stress to the control sample, and improved results compared with Gen-Os. The presented preliminary biocompatibility results are promising for bone tissue regeneration applications of HA1, and the study will continue with further tests on osteoblast differentiation and mineralization.

In this study, zinc oxide nanoparticles were synthesized through a simple co-precipitation method starting from zinc acetate dihydrate and sodium hydroxide as reactants. The as-obtained ZnO nanoparticles were morphologically and structurally characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), photocatalytic activity, and by determining the antimicrobial activity against Gram-negative and Gram-positive bacteria. The XRD pattern of the zinc oxide nanoparticles showed the wurtzite hexagonal structure, and its purity highlighted that the crystallinity correlated with the presence of a single product, zinc oxide. The ZnO nanoparticles have an average crystallite size of 19 ± 11 nm, which is in accordance with the microscopic data. ZnO nanoparticles were tested against methyl orange, used as a model pollutant, and it was found that they exhibit strong photocatalytic activity against this dye. The antibacterial activity of ZnO nanoparticles was tested against Gram-negative and Gram-positive strains (Escherichia coli, Staphylococcus aureus, and Candida albicans). The strongest activity was found against Gram-positive bacteria (S. aureus).

The nanostructured cobalt aluminate (CoAl2O4) was obtained through an eco-friendly precursor method using aqueous extract of tamarind fruit. The use of plant extracts is a simple and effective approach for the preparation of CoAl2O4 nanoparticles. The polynuclear complex precursor was characterized by Fourier transform infrared spectroscopy (FTIR), ultraviolet–visible spectroscopy (UV–VIS) and thermal analysis. The cobalt aluminate was investigated by: X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), FTIR, UV–VIS and colour measurements by reflectance spectroscopy (RS). X-ray diffraction patterns confirmed the formation of cubic CoAl2O4 spinel phase with good crystallinity. The average particle size from TEM is about 71 nm. Chromatic coordinates indicate that the bluest colour was obtained for the cobalt aluminate obtained by subsequent heat treatment.

The Fe3O4/Ag/C nanocomposite was successfully prepared by combustion synthesis using citric acid as fuel. The composition, morphology and structure of the nanocomposite were investigated by Mossbauer spectroscopy, X-ray diffraction (XRD), thermogravimetric (TG)/differential scanning calorimetry (DSC), scanning electron microscopy (SEM)-energy dispersive X-ray (EDX), transmission electron microscopy (TEM) and N2 adsorption-desorption technique. The magnetic nanocomposite was tested as adsorbent for the removal of Methylene Blue, Acid Orange 7 and Rhodamine 6G in single and multi-component system from aqueous solutions. The effects of solution pH, contact time, adsorbent dose, and initial pollutants concentration on the dyes adsorption were studied. It was demonstrated that working in normal conditions, i.e. solution pH and room temperature (25 °C), removal percentage higher than 90% for single and binary-systems and higher than 75% for ternary-systems was obtained. Adsorption kinetic results showed that pseudo-second-order model describe the experimental data/adsorption process in single and multiple-solute systems. From the Sips isotherm model the maximum adsorption capacities in single systems were determined. The advantage of obtaining low-cost Fe3O4/Ag/C nanocomposite with good adsorption capacity and easy magnetic separation, effective in single and multi-component adsorption of both cationic and anionic dyes, represent a strong argument regarding its great potential for practical applications.

Ceramic scaffolds were prepared starting from a sol–gel powder, which was mixed with glucose as a pore-generating substance and subsequently thermally treated at different temperatures and for different periods in order to ensure the formation of a resistance structure. The final materials were characterized in terms of structure, morphology, and biological properties by employing X-ray diffraction, scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy, immersion in simulated body fluid, and specific cellular tests on mesenchymal stem cells (optical microscopy, MTT, and GSH assays). The results showed the occurrence of akermanite as the main crystalline phase in all scaffolds. The porosity and compression strength of these 3D architectures can be adjusted through the thermal treatment parameters. Moreover, the biological evaluation indicated an excellent bioactivity and a good biocompatibility at short term for all samples.

For more than five decades, alkali niobate-based materials (KxNa1−xNbO3) have been one of the most promising lead-free piezoelectric materials researched to be used in electronics, photocatalysis, energy storage/conversion and medical applications, due to their important health and environmentally friendly nature. In this paper, our strategy was to synthetize the nearest reproductible composition to KxNa1−xNbO3 (KNN) with x = 0.5, placed at the limit of the morphotropic phase boundary (MPB) with the presence of both polymorphic phases, orthorhombic and tetragonal. The wet synthesis route was chosen to make the mix crystal powders, starting with the suspension preparation of Nb2O5 powder and KOH and NaOH alkaline solutions. Hydrothermal microwave-assisted maturation (HTMW), following the parameter variation T = 200–250 °C, p = 47–60 bar and dwelling time of 30–90 min, was performed. All powders therefore synthesized were entirely KxN1−xNbO3 solid solutions with x = 0.06–0.69, and the compositional, elemental, structural and morphological characterization highlighted polycrystalline particle assemblage with cubic and prismatic morphology, with sizes between 0.28 nm and 2.95 μm and polymorphic O-T phase coexistence, and a d33 piezoelectric constant under 1 pC/N of the compacted unsintered and unpoled discs were found.

Aluminum hydroxide is an essential material for the industrial production of ceramics (especially insulators and refractories), desiccants, absorbents, flame retardants, filers for plastics and rubbers, catalysts, and various construction materials. The calcination process of Al(OH)3 first induces dehydration and, finally, results in α-Al2O3 formation. Nevertheless, this process contains various intermediary steps and has been proven to be complicated due to the development of numerous transitional alumina. Each step of the investigation is vital for the entire process because the final properties of materials based on aluminum trihydroxide are determined by their phase composition, morphology, porosity, etc. In this paper, five dried, milled, and size-classified aluminum hydroxide specimens were thermally treated at 260, 300, and 400 °C, then, they were studied in order to identify the effects of temperature on their properties, such as particle morphology, specific surface area, pore size, and pore distribution. The major oxide compounds identified in all samples were characteristic of bauxite—namely, Al2O3 * 3H2O, SiO2, Fe2O3, Na2O, and CaO. Particles with smaller sizes (&lt, 10 µm = 76.28%) presented the highest humidity content (~5 wt.%), while all samples registered a mass loss of ~25 wt.% on ignition at 400 °C. The identified particles had the shapes of hexagonal or quasi-hexagonal platelets and resulted in large spherulitic concretions. The obtained results suggest that ceramic powders calcined at 400 °C should be used for applications as adsorbents or catalysts due to their high specific area of about 200–240 m2/g and their small pore width (3–3.5 nm).

Herein we report on novel multiferroic core&ndash, shell nanostructures of cobalt ferrite (CoFe2O4)&ndash, bismuth, sodium titanate doped with barium titanate (BNT&ndash, BT0.08), prepared by a two&ndash, step wet chemical procedure, using the sol&ndash, gel technique. The fraction of CoFe2O4 was varied from 1:0.5 to 1:1.5 = BNT&ndash, BT0.08/CoFe2O4 (molar ratio). X&ndash, ray diffraction confirmed the presence of both the spinel CoFe2O4 and the perovskite Bi0.5Na0.5TiO3 phases. Scanning electron microscopy analysis indicated that the diameter of the core&ndash, shell nanoparticles was between 15 and 40 nm. Transmission electron microscopy data showed two&ndash, phase composite nanostructures consisting of a BNT&ndash, BT0.08 core surrounded by a CoFe2O4 shell with an average thickness of 4&ndash, 7 nm. Cole-Cole plots reveal the presence of grains and grain boundary effects in the BNT&ndash, BT0.08/CoFe2O4 composite. Moreover, the values of the dc conductivity were found to increase with the amount of CoFe2O4 semiconductive phase. Both X-ray photoelectron spectroscopy (XPS) and M&ouml, ssbauer measurements have shown no change in the valence of the Fe3+, Co2+, Bi3+ and Ti4+ cations. This study provides a detailed insight into the magnetoelectric coupling of the multiferroic BNT&ndash, BT0.08/CoFe2O4 core&ndash, shell composite potentially suitable for magnetoelectric applications.

One of the most promising ways for the realization of multi-functional materials is the integration of oxides with different properties in artificial heterostructures. In this paper, a novel piezoelectric-ferromagnetic heterostructure consisting of 0.92Na(0.5)Bi(0.5)TiO(3)-0.08BaTiO(3) (abbreviated as BNT-BT0.08) and CoFe2O4 layers is fabricated on Si-Pt substrate, by sol-gel method coupled with spin-coating technique. The composite thin film shows only perovskite Bi0.5Na0.5TiO3-like rhombohedral phase and CoFe2O4 cubic phase. The thickness of CoFe2O4 and BNT-BT0.08 layers is similar to 280 and similar to 400 nm, respectively. BNT-BT0.08/CoFe2O4 heterostructure thin film shows a saturation magnetization of 0.11 emu/g at 5 K and 0.07 emu/g at 295 K, dielectric constant of 235 at 1 kHz and tunability of 70% at 1 kHz and an electric field E = 110 kV/cm. The results reveal that the investigated hybrid piezoelectric/ferromagnetic structure shows piezoelectric behavior, good ferroelectric and ferromagnetic properties. This bilayer composite can be used in miniature low-frequency magnetic sensor and piezoelectric sensor for biomedical domain.

Multifunctional materials integrating optical and electric properties into a composite or into a doped single–phase material have attracted much attention from scientists for future optoelectronic devices. In this work, polycrystalline Ba1–xTbxTiO3, x = 0.00, 0.01 and 0.05 materials were synthesized by hydrothermal route and their photoluminescence and dielectric properties were studied. The as–prepared powders showed a microstructure consisting of grains with the shape of cube; and average particle size ranging from 75 nm to 150 nm. The investigated temperature dependence of dielectric permittivity of Ba1–xTbxTiO3 ceramics revealed a decrease of the Curie temperature (Tc) with increasing terbium content, and a more pronounced degree of diffuseness of phase transition. The resistivity at room temperature was discussed in terms of positive temperature coefficient of resistance (PTRC) effect. UV–vis reflectance spectra of Ba1–xTbxTiO3 samples showed a decrease of the band gap energy with the increase of Tb amount, due to the band–gap narrowing effect. The photoluminescence spectra recorded for Tb doped BaTiO3 materials, at 80 K, evidenced the typical f–f luminescence lines of the Tb3+ accompanied the broad luminescence band at about 425 nm due to self–trapped exciton recombination. These results demonstrated that the terbium enhances the dielectric properties and photoluminescence simultaneously, being suitable for electronic applications.

In this work, we report on the synthesis and characterization of BNT-BT0.08/CoFe2O4 biphasic composite with core-shell structure. This artificial core (BNT-BT0.08)/shell (CoFe2O4) heterostructure was prepared by sol-gel method and the resulting composite was characterized in term of microstructure, dielectric, piezoelectric and magnetic properties. BNT-BT0.08/CoFe2O4 sintered ceramic shows high permittivity (e′ ≥ 30) and high dielectric losses (tan δ ≥ 10) in the low frequency range (ν ≤ 104 Hz), remnant polarization (Pr) of ∼7.7 μC/cm2 and, remanent magnetization (Mr) of 24 emu/g at 5 K and of 14 emu/g, at room temperature. The present study reveals that the ferroelectric, piezoelectric and magnetic properties of this new architectured composite depend on the amount of each component and, can be tailored by adjusting their synthesis conditions. BNT-BT0.08/CoFe2O4 core-shell material investigated in this work provides a novel way to exploit new applications for the multifunctional composite, such as piezoelectric sensor, magnetoelectronic sensors and data storage devices.

Starting from SiO2–CaO–P2O5–ZnO–CaF2 oxide system, vitroceramic materials were obtained by employing the sol-gel approach, followed by thermal treatment in order to provide, in a controlled manner, the nucleation and growth of crystalline phases in the parent glassy matrix. Thermal analysis, X-ray diffraction, scanning electron microscopy, energy dispersive X-ray spectroscopy, transmission electron microscopy, selected area electron diffraction and Fourier transformed infrared spectroscopy were employed for the characterization of the resulting samples. The sintered vitroceramics present calcium silicates as crystallized nano-domains and a porosity that decreases with the enhancement of the processing temperature. The assessment of the biological properties was carried out in vitro by simulated body fluid immersion for 14 days, associated with a detailed analysis of the apatitic layer formed on the surface.

The influence of nickel substitutions on the local structure, dielectric and magnetic properties of Ba hexaferrites is investigated in this study for use as rare earth free permanent magnets and microwave devices, especially. For this purpose, BaNixFe12–xO19 (x = 0.0, 0.2, 0.5, 0.8 and 1.0) powders were prepared by auto–combustion of their citrate–nitrate gels precursor whilst spark plasma sintering and conventional sintering techniques were used in order to prepare BaNixFe12–xO19 sintered ceramics samples. Structure, microstructure, dielectric and magnetic properties of BaNixFe12–xO19 materials were investigated by X-ray diffraction, scanning electron microscopy (SEM), dielectric measurements, Mossbauer spectroscopy and SQUID magnetometry. X-ray diffraction analyses indicated that BaNixFe12–xO19, x = 0.0–1.0crystallized on the hexagonal BaFe12O19 structure and, the lattice parameters a and c, decrease as the Ni content increases. Raman spectroscopy analysis confirmed the formation of the BaFe12O19 phase. The presence of Fe in the +3 oxidation state (Fe3+) and of Ni2+ is confirmed by X-ray photoelectron spectroscopy (XPS). The SEM investigations on BaNixFe12–xO19 powders showed the change of the morphology from a granular-like structure to a platelet-like structure with increasing the nickel content which influences the dielectric and magnetic properties of these materials. Dielectric measurements performed on BaFe12−xNixO19 ceramics showed consistent differences between the two sintering methods. Impedance analysis shows a contribution of grains and grain boundaries in all samples. The Mossbauer spectroscopy results evidenced the five Wyckoff crystallographic iron positions and their site occupancy with respect to Ni substitutions content. The permanent magnet characteristics of the hexaferrites were confirmed by the high values of coercive field (up to ∼ 1.7 kOe) and remanence (∼28 emu/g), while the saturation magnetization values are found up to 95 emu/g at low temperatures and 70 emu/g at room temperature (for x = 0.8). The coercive field, remanence and maximum energy product decrease with nickel content, while the saturation magnetization behaves unmonotonically due to the specific variation of the site occupancy. More insight into the link between local structure and magnetic properties of Ni substituted Ba hexaferrite was given.

This paper is focused on the basic properties of ceramic composite materials used as thermal barrier coatings in the aerospace industry like SiC, ZrC, ZrB2 etc., and summarizes some principal properties for thermal barrier coatings. Although the aerospace industry is mainly based on metallic materials, a more attractive approach is represented by ceramic materials that are often more resistant to corrosion, oxidation and wear having at the same time suitable thermal properties. It is known that the space environment presents extreme conditions that challenge aerospace scientists, but simultaneously, presents opportunities to produce materials that behave almost ideally in this environment. Used even today, metal-matrix composites (MMCs) have been developed since the beginning of the space era due to their high specific stiffness and low thermal expansion coefficient. These types of composites possess properties such as high-temperature resistance and high strength, and those potential benefits led to the use of MMCs for supreme space system requirements in the late 1980s. Electron beam physical vapor deposition (EB-PVD) is the technology that helps to obtain the composite materials that ultimately have optimal properties for the space environment, and ceramics that broadly meet the requirements for the space industry can be silicon carbide that has been developed as a standard material very quickly, possessing many advantages. One of the most promising ceramics for ultrahigh temperature applications could be zirconium carbide (ZrC) because of its remarkable properties and the competence to form unwilling oxide scales at high temperatures, but at the same time it is known that no material can have all the ideal properties. Another promising material in coating for components used for ultra-high temperature applications as thermal protection systems is zirconium diboride (ZrB2), due to its high melting point, high thermal conductivities, and relatively low density. Some composite ceramic materials like carbon−carbon fiber reinforced SiC, SiC-SiC, ZrC-SiC, ZrB2-SiC, etc., possessing low thermal conductivities have been used as thermal barrier coating (TBC) materials to increase turbine inlet temperatures since the 1960s. With increasing engine efficiency, they can reduce metal surface temperatures and prolong the lifetime of the hot sections of aero-engines and land-based turbines.

We investigated in this paper a novel bilayer composite obtained by sol-gel and spin coating of the ferroelectric 0.92Na0.5Bi0.5TiO3–0.08BaTiO3 (abbreviated as BNT-BT0.08) and ferromagnetic CoFe2O4 phases, for miniature low-frequency magnetic sensors and piezoelectric sensors. This heterostructure, deposited on Si-Pt substrate (Si-Pt/CoFe2O4/BNT-BT0.08), was characterized using selected method such as: X-ray diffraction, dielectric spectroscopy, piezoelectric force microscopy, SQUID magnetometry, atomic force microscopy/magnetic force microscopy, and advanced methods of transmission electron microscopy. CoFe2O4/BNT-BT0.08 ferromagnetic–piezoelectric thin films show good magnetization, dielectric constant and piezoelectric response. The results of analyses and measurements reveal that this heterostructure can have applications in high-performance magnetoelectric devices at room temperature.

In this work we report on a new 1-1 composite coaxial nanostructure containing nanotubes of CoFe 2 O 4 and BNT-BT 0.08 prepared by a template-based fabrication technique using the sol-gel chemistry. In this regard, CoFe 2 O 4 /BNT-BT 0.08 core-shell nanotubes were prepared using a polycarbonate membrane template and sols precursors of CoFe 2 O 4 and BNT-BT 0.08 . The deposition of nanotubes was performed by pore wetting of the porous membranes via capillary action and subsequent pyrolysis. The studies with scanning electron microscopy and transmission electron microscopy (TEM) revealed that the composite material is characterized by the 1-D tubular structure. Analysis by X-ray diffraction, high-resolution TEM imaging and selected-area electron diffraction pattern demonstrated that the synthetic composite nanotube CoFe 2 O 4 /BNT-BT 0.08 has crystalline structure with cubic CoFe 2 O 4 and rhombohedral BNT-BT 0.08 phases. CoFe 2 O 4 /BNT-BT 0.08 coaxial nanotubes show dielectric properties, piezoelectric and ferromagnetic behavior.