Synthesis and characterization of nanometric gadolinia powders by room temperature solid-state displacement reaction and low temperature calcination

Nanometric-sized gadolinia (Gd₂O₃) powders were obtained by applying solid-state displacement reaction at room temperature and low temperature calcination. The XRD analysis revealed that the room temperature product was gadolinium hydroxide, Gd(OH)₃. In order to induce crystallization of Gd₂O₃, the subsequent calcination at 600 ∼ 1200 °C of the room temperature reaction products was studied. Calculation of average crystallite size (D) as well as separation of the effect of crystallite size and strain of nanocrystals was performed on the basic of Williamson-Hall plots. The morphologies of powders calcined at different temperatures were followed by scanning electron microscopy. The pure cubic Gd₂O₃ phase was made at 600 °C which converted to monoclinic Gd₂O₃ phase between 1400° and 1600 °C. High-density (96% of theoretical density) ceramic pellet free of any additives was obtained after pressureless sintering at 1600 °C for 4 h in air, using calcined powder at 600 °C.     

Signature of multiferroicity and pyroelectricity close to room temperature in BaFe12O19 hexaferrite

In this paper, we have reported the signature of multiferroicity and pyroelectricity in BaFe₁₂O₁₉ hexaferrite close to room temperature. The BaFe₁₂O₁₉ hexaferrite samples are synthesized by co-precipitation method at different sintering temperature ranging from 800 to 1200 °C and study their structural, ferroelectric, magnetic, magnetoelectric and pyroelectric properties. X-ray Diffraction patterns show the pure phase formation for all samples. Morphological changes are examined through the scanning electron microscope. The maximum ferroelectric polarization (0.66 μC/cm²) is observed for the sample sintered at 1200 °C, however maximum magnetic polarization 74 emu/g is observed for sample sintered at 1000 °C. Magneto-electric coupling measurements are also performed through dynamic method and average magneto-electric coupling coefficient (~ 7.05 × 10⁻⁷ mV/cm Oe²) is observed at room temperature for the sample sintered at 1200 °C. Furthermore, maximum pyroelectric constant (147 × 10⁻¹³C/cm² °C) is observed at 75 °C for BaFe₁₂O₁₉ samples sintered at 1200 °C. The observation of both multiferroicity and pyroelectricity close to room temperature in BaFe₁₂O₁₉ hexaferrite is interesting and useful for multifunctional devices.     

Microstructure and dielectric properties of the Ti-rich BaO–TiO2 thin films for microwave devices

Ti-rich BaO–TiO₂ thin films were grown on a Pt/Ti/SiO₂/Si substrate using rf sputtering and the structural and dielectric properties of the films were investigated. For the film grown at room temperature and rapidly thermal annealed (RTA) at 900 °C for 3 min, an amorphous phase with a small BaTi₅O₁₃ crystalline phase was formed. As the growth temperature increased, the amount of the BaTi₅O₁₁ crystalline phase increased. For the film grown at 350 °C and RTA at 900 °C for 3 min, the homogeneous BaTi₅O₁₁ phase was formed. The BaTi₄O₉ phase was developed when the growth temperature exceeded 450 °C. The thin film with the homogeneous BaTi₄O₉ phase was obtained when the film was grown at 550 °C and RTA at 900 °C for 3 min. The dielectric properties of the films were measured at 1–6 GHz range. The dielectric constant (ϵ_r) of the BaTi₅O₁₁ film was about 33 and the dissipation factor was about 0.01. The ϵ_r and the dissipation factor of the BaTi₄O₉ film were about 37 and 0.005, respectively.     

Effect of calcination temperature on the fabrication of transparent lutetium titanate by spark plasma sintering

Transparent lutetium titanate (Lu₂Ti₂O₇) bodies were fabricated by spark plasma sintering using Lu₂O₃ and TiO₂ powders calcined from 700 °C to 1200 °C. No solid-state reaction was identified after calcination at 700 °C, whereas single-phase Lu₂Ti₂O₇ powder was prepared at 1100 and 1200 °C. The calcination at 700 °C promoted densification at the early stages of sintering, whereas residual pores at grain boundaries resulted in Lu₂Ti₂O₇ bodies with low transparency. Low-density and opaque Lu₂Ti₂O₇ bodies formed owing to the coarsening of the powder calcined at 1200 °C. The Lu₂Ti₂O₇ body sintered using the powder calcined at the moderate temperature of 1100 °C had a density of 99.5% with the highest transmittances of 41% and 74% at wavelengths of 550 nm and 2000 nm, respectively.     

Low temperature sintering and microwave dielectric properties of TiO2 ceramics

The TiO₂ ceramics were prepared by a solid-state reaction in the temperature range of 920–1100 °C for 2 h and 5 h using TiO₂ nano-particles (Degussa-P25 TiO₂) as the starting materials. The sinterability and microwave properties of the TiO₂ ceramics as a function of the sintering temperature were studied. It was demonstrated that the rutile phase TiO₂ ceramics with good compactness could be readily synthesized from the Degussa-P25 TiO₂ powder in the temperature range of 920–1100 °C without the addition of any glasses. Moreover, the TiO₂ ceramics sintered at 1100 °C/2 h and 920 °C/5 h demonstrated excellent microwave dielectric properties, such as permittivity (Ɛ_r) value >100, Q × f  > 23,000 GHz and τ_f ≅ 200 ppm/°C.     

Densification behavior and properties of alumina–chrome ceramics: Effect of TiO2

Highly dense alumina–chrome bodies with low porosity are usually used as corrosion and thermal resistant refractories. Alumina–chrome refractory with molar ratio 1:1 was developed using chemical grade hydrated alumina and chromium (III) oxide by conventional sintering route. Batch materials were attrition milled, isostatically pressed and sintered in the temperature range from 1000 °C to 1700 °C with 2 h soaking at peak temperature. Phase development of the sintered materials with temperature was studied by X-ray diffraction. Sintering temperature, sintering condition and addition of sintering aid (TiO₂) have immense effect on the densification of the alumina–chrome refractory. Highly dense alumina–chrome refractory with almost nil apparent porosity was developed at 1500 °C in reducing atmosphere. Flexural strength of the sintered materials at room temperature and at 1200 °C was also measured. 1 wt% TiO₂ gives the optimum result with respect to densification and flexural strength.     

Fracture toughness,strength and creep of transparent ceramics at high temperature

Fracture toughness, four-point bending strength of transparent spinel, Y₂O₃ and YAG ceramics in function of temperature (from room temperature up to 1500° C) were measured. Creep resistance at 1500–1550° C was studied too. Grain size distribution was determined on polished and etched surfaces of samples. Fracture surfaces after tests were examined by scanning electron microscopy. The obtained results showed that: in the case of spinel ceramics fracture toughness and strength decreased from 20 to 800° C, increased from 800 to 1200° C and decreased at higher temperature; in the case of Y₂O₃ ceramics they increased from 400 to 800° C, and next kept constant up to 1500° C; in the case of YAG ceramics they kept constant from 20 to 1200° C and then decreased. The creep strain rate was measured for spinel and YAG but not for Y₂O₃ ceramics which appeared creep resistant. The hypotheses concerning toughening and creep mechanisms were proposed.     

Preparation of cerium titanate brannerite by solution combustion,and phase transformation during heat treatment

An aqueous solution route was employed to prepare cerium titanate oxide brannerite. Thermal analysis, X-ray diffraction, Raman spectroscopy, transmission and scanning electron spectroscopy, were used to investigate the brannerite structure formation and bulk properties. Mixed metal oxides (TiO₂, CeO₂ and brannerite CeTi₂O₆) were formed upon calcination at 800 °C for 12 h. The amount of brannerite phase decreased to form the constituent oxides with increasing calcination temperature and only pure TiO₂ and CeO₂ were present after 1200 °C calcination. The brannerite CeTi₂O₆ phase reformed at 1300 °C, and its relative amount was increased with dwell time. After 48 h calcination at 1300 °C, brannerite with only minor metal oxide impurities (<1%) was observed. The sample melted at 1400 °C which led to the collapse of brannerite back to its constituent oxides. Further, the phase formation was influenced by pelletization of the powders, which may be explained by a molar volume increase during brannerite formation. Attempts to confirm this hypothesis using Pu brannerite were inconclusive.     

Enhanced activity of MnxW0.05Ti0.95 − xO2 − δ for selective catalytic reduction of NOx with ammonia by self-propagating high-temperature synthesis

A series of TiO₂ supported MnWO_x catalysts Mn_xW_0.05Ti_0.95 − xO_2 − δ (x = 0.05, 0.1, 0.15) were synthesized by solution combustion method. The Mn_0.10W_0.05Ti_0.85O_2 − δ catalyst showed highest activity in NH₃-SCR reaction within a broad temperature range of 200 °C–400 °C. XRD and TEM results indicate that the active Mn and W species are highly dispersed over TiO₂ support in the form of nanoparticles (4–7 nm). The TEM and H₂-TPR results also suggest that a MnWO_x phase has been formed on the TiO₂, which is beneficial for the activity of the Mn_xW_0.05Ti_0.95 − xO_2 − δ catalysts in the high temperature range of 280 °C–400 °C.     

Microstructure and mechanical properties of ceramics obtained from chemically co-precipitated Al2O3-GdAlO3 nano-powders with eutectic composition

An efficient and flexible chemical co-precipitation method has been used to synthesize nanoscale Al₂O₃-GdAlO₃ powders with eutectic composition. The as-synthesized powders exhibit a highly dispersive and homogeneous distribution with an average particle size of 50 nm. The phase transition in the resulting powders strongly depends upon the calcination temperature. GdAlO₃ undergoes complete crystallization after calcination at 1050 °C, however, the diffraction peaks of α-Al₂O₃ are found at a relatively high calcination temperature of at least 1300 °C. The fully-densified Al₂O₃-GdAlO₃ ceramic with eutectic composition obtained by hot pressing the nanoscale powders at 1500 °C exhibits a room temperature flexural strength of 556 MPa, a Vickers hardness of 17.3 GPa and a fracture toughness of 7.5 MPa m^1/2. The high temperature flexural strength of the as-sintered Al₂O₃-GdAlO₃ ceramic is measured to be 515 MPa after bending tests at 1000 °C.     

Tribological properties of NiCr–ZrO2(Y2O3)–SrSO4 composites at elevated temperatures

The effect of SrSO₄ content on the tribological properties of NiCr–30wt%ZrO₂(Y₂O₃) (NC30Z) cermet was evaluated over a wide temperature range from room temperature to 1000 °C. The results indicated that the inclusion of SrSO₄ effectively improved the friction coefficients and wear rates of NC30Z cermet above 400 °C. NC30Z–5SrSO₄ composite against alumina ball exhibited satisfactory tribological performance, which was attributed to synergistic lubrication of pseudocubic-SrZrO₃ and NiCr₂O₄ between 400 °C and 800 °C and cubic-SrZrO₃, NiCr₂O₄, NiO and Cr₂O₃ at 1000 °C.     

Sintering mechanisms of Yttria with different additives

The sintering behaviour of conventional yttria powder was investigated, with emphasis on the effect of sintering additives such as B₂O₃, YF₃, Al₂O₃, ZrO₂, and TiO₂, etc. at sintering temperatures from 1000 °C to 1600 °C. Powder shrinkage behaviour was analysed using a dilatometer. The powder sintering mechanisms were identified at different temperatures using powder isothermal shrinkage curves. This analysis showed that the sintering additives B₂O₃ and YF₃ could improve yttria sintering by changing the diffusion/sintering mechanisms at certain temperatures, while sintering additives TiO₂, Al₂O₃ and ZrO₂ appeared to retard the powder densification at temperatures around 1000 °C and are more suitable when used at temperatures in excess of 1300 °C. The powder with La₂O₃ added had the slowest densification rate throughout the test temperatures in this experiment and was also found to be more suitable when used at temperatures higher than 1550 °C.     

Microwave dielectric properties of LiNb3O8 ceramics with TiO2 additions

The microwave dielectric properties of LiNb₃O₈ ceramics were investigated as a function of the sintering temperature and the amount of TiO₂ additive. LiNb₃O₈ ceramics, which were calcined at 750 °C and sintered at 1075 °C for 2 h, showed a dielectric constant (ɛ_r) of 34, a quality factor (Q × f₀) of 58,000 GHz and a temperature coefficient of resonance frequency (τ_f) of −96 ppm/°C, respectively. The density of the samples influenced the properties of these properties. As the TiO₂ content increased in the LiNb₃O₈–TiO₂ system, ɛ_r and τ_f of the material were increased due to the mixing effect of TiO₂ phase, which has higher dielectric constant and larger positive τ_f. The 0.65LiNb₃O₈–0.35TiO₂ ceramics showed a dielectric constant ɛ_r of 46.2, a quality factor (Q × f₀) of 5800 GHz and a temperature coefficient of resonance frequency τ_f of near to 0 ppm/°C.     

Synthesis and enhanced gas sensing properties of flower-like ZnO/α-Fe2O3 core-shell nanorods

This paper reports a facile two-step synthesis route for the preparation of flower-like ZnO/α-Fe₂O₃ nanorods (NRs). Flower-like ZnO NRs with the average diameter about 810 nm and length about 4.5 µm were firstly synthesized via a chemical solution method, and then ZnO NRs was coated with a continuous α-Fe₂O₃ layer to form ZnO/α-Fe₂O₃ core-shell structure through an ionic-layer adsorption and reaction method. The gas-sensing results show that the ZnO/α-Fe₂O₃ NRs exhibit excellent sensitivity, selectivity, and response-recovery capacity to ethanol vapor at a low optimum temperature of 240 °C. In particular, compared with pure ZnO NRs and α-Fe₂O₃ nanoparticles (NPs), the ZnO/α-Fe₂O₃ NRs show an obvious improvement in gas sensing properties. The substantial improvement of sensing properties may be attributed to the unique microstructure and heterojunction formed between ZnO and α-Fe₂O₃.     

Probing the oxidation behavior of Ti2AlC MAX phase powders between 200 and 1000 °C

Oxidation of commercial Ti₂AlC MAX phase powders at 200–1000 °C has been investigated by XRD, XPS, SEM, STA and TGA coupled with FTIR. These powders are a mixture of Ti₂AlC, Ti₃AlC₂, TiC and Ti_1.2Al_0.8. Oxidation at 400 °C led to disappearance of carbide phases from Ti 2p, Al 2p and C 1s XPS spectra. At 600 °C, powders changed from dark grey to light grey with a significant volume increase due to crack formation. Powders were severely oxidized by detecting rutile with minor anatase TiO₂. At 800 °C, α-Al₂O₃ was detected while anatase transformed into rutile TiO₂. The cracks were healed and disappeared. At 1000 °C, the Ti₂AlC powders were fully oxidized into rutile TiO₂ and α-Al₂O₃ with a change of powder color from light grey to yellow. FTIR detected the release of C as CO₂ from 200 °C onwards but with additional CO above 800 °C.     

Thermal properties of La2O3-doped ZrB2- and HfB2-based ultra-high temperature ceramics

Thermal properties of La₂O₃-doped ZrB₂- and HfB₂-based ultra high temperature ceramics (UHTCs) have been measured at temperatures from room temperature to 2000 °C and compared with SiC-doped ZrB₂- and HfB₂-based UHTCs and monolithic ZrB₂ and HfB₂. Thermal conductivities of La₂O₃-doped UHTCs remain constant around 55–60 W/mK from 1500 °C to 1900 °C while SiC-doped UHTCs showed a trend to decreasing values over this range.     

Preparation and characterisation of mixed matrix Al2O3- and TiO2-based ceramic membranes prepared using polymeric synthesis route

Al₂O₃- and TiO₂-based ceramic membranes prepared using polymeric synthesis route were characterized by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy, X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR) and gas permeability tests. The influence of the final calcination temperature and the systematic investigation of the properties of the membranes are provided. The calcination temperature affected morphological, structural and chemical properties, as well as the gas permeability of the ceramic membranes. XRD analysis revealed rhombohedral and tetragonal structures of Al₂O₃ and TiO₂-based ceramic, respectively, prepared at calcination temperatures of 1100 and 1200 °C. The TiO₂-based ceramic matrix calcined at temperatures of 1100 and 1200 °C exhibited a well-defined crystalline microstructure with the grains increasing in size as a function of temperature. FTIR analysis revealed that phosphorus additives in orthoclase clay tend to form phosphonate groups during the calcination process. The decomposition of organic source was not fulfilled as tested at calcination temperatures of 1000, 1100 and 1200 °C.     

Effect of annealing on the structure and magnetic properties of mechanically milled TiO2–Fe2O3 mixture

A mixture of Fe₂O₃ and TiO₂ oxides has been mechanically milled to form TiFe₂O₄ spinel phase. X-ray diffraction (XRD) pattern of the as-milled mixture shows the presence of both Fe₂O₃ and TiO₂ phases. The diffraction peaks become broader and their relative intensity drastically decreases due to the particle size reduction and accumulation of strains. The milled powder was then subjected to annealing at different temperatures (600, 750, 900, 1200 °C). Annealing at 600 °C and 750 °C does not show any significant change in the phase formation. Nonetheless, XRD patterns show a narrowing and an increase in the intensity of Fe₂O₃ peaks with respect to TiO₂, which was reflected by an evolution in particle nano-structure following SEM analysis. An increase in the intensity ratio of the major peaks belonging to Fe₂O₃ relative to the as-milled mixture, which was associated with a reduction of the amount of TiO₂, suggested a possible insertion of Ti into the Fe₂O₃ crystal lattice. However, in VSM measurements, annealing at 600 °C and 750 °C does not change the ferromagnetic phase but the effect of annealing was a notable reduction in the values of both Ms and Mr (saturation magnetization and remanence magnetization respectively) Ultimately, as the powder was heated to 900 °C a new phase seemed to have emerged, this phase was confirmed by SEM, XRD, and magnetic measurements (VSM) where it change phase from ferromagnetic to paramagnetic phase.     

A novel low-firing microwave dielectric ceramic Li2ZnGe3O8 with cubic spinel structure

A Li₂ZnGe₃O₈ ceramic was investigated as a promising microwave dielectric material for low-temperature co-fired ceramics applications. Li₂ZnGe₃O₈ ceramic was prepared via the conventional solid-state method. X-ray diffraction data shows that Li₂ZnGe₃O₈ ceramic crystallized into a cubic spinel structure with a space group of P4₁32. Dense ceramic with a relative densities of 96.3% were obtained when sintered at 945 °C for 4 h and exhibited the optimum microwave properties with a relative permittivity (ε_r) of 10.3, a quality factor (Q × f) of 47,400 GHz (at 13.3 GHz), and a temperature coefficient of resonance frequency (τ_f) of −63.9 ppm/°C. The large negative τ_f of Li₂ZnGe₃O₈ ceramic could be compensated by rutile TiO₂, and 0.9Li₂ZnGe₃O₈–0.1TiO₂0·1TiO₂ ceramic sintered at 950 °C for 4 h exhibited improved microwave dielectric properties with a near-zero τ_f of −1.6 ppm/°C along with ε_r of 11.3 and a Q × f of 35,800 GHz (11.6 GHz). Moreover, Li₂ZnGe₃O₈ was found to be chemically compatible with silver electrode when sintered at 945 °C.     

Protective properties of Al2O3 + TiO2 coating produced by the electrostatic spray deposition method

Mechanical resistance of Al₂O₃ + TiO₂ nanocomposite ceramic coating deposited by electrostatic spray deposition method onto X10CrAlSi18 steel to thermal and slurry tests was investigated. The coating was produced from colloidal suspension of TiO₂ nanoparticles dispersed in 3 wt% solution of Al₂(NO₃)₃, as Al₂O₃ precursor, in ethanol. TiO₂ nanoparticles of two sizes, 15 nm and 32 nm, were used in the experiments. After deposition, coatings were annealed at various temperatures, 300, 1000 and 1200 °C, and next exposed to cyclic thermal and slurry tests. Regardless of annealing temperature and the size of TiO₂ nanoparticles, the outer layer of all coatings was porous. The first five thermal cycles caused a rapid increase of aluminum content of the surface layer to 30–37 wt%, but further increase in the number of thermal cycles did not affect the aluminum content. The oxidation rate of coating-substrate system was lower during the thermal tests than during annealing. The oxidation rate was also lower for smaller TiO₂ particles (15 nm) forming the coating than for the larger ones (32 nm). The protective properties of Al₂O₃ + TiO₂ coating against intense oxidation of substrate were lost at 1200 °C. Slurry tests showed that coatings annealed at 1000 °C had the best slurry resistance, but thermal tests had weakened this slurry resistance, mainly due to decreasing adhesion of the coating.