Grain-Boundary Wetting-Dewetting in z= 1 SiAlON Ceramic

The grain-boundary structure of a model SiAlON polycrystal with nominal composition Si₅AlON₇ was characterized by transmission electron microscopy (TEM) both in an equilibrium (as-processed) state at room temperature and after quenching from elevated temperature. In addition, low-frequency (1–13 Hz) internal friction data were recorded as a function of temperature, showing a pronounced grain-boundary sliding peak positioned at 1030°C. High-resolution transmission electron microscopy (HRTEM) of the equilibrated low-temperature microstructure revealed residual glass only at multigrain junctions, but no amorphous intergranular films were observed. The detection of clean interfaces in the as-processed sample contradicts the internal friction data, which instead suggests the presence of a low-viscosity grain boundary phase, sliding at elevated temperatures. Therefore, a thin section of the as-sintered material was heated to 1380°C and rapidly quenched. HRTEM analysis of this sample showed, apart from residual glass pockets, wetted grain boundaries, which is in line with the internal friction experiment. This wetting-dewetting phenomenon observed in z = 1 SiAlON is expected to have a strong impact not only on high-temperature engineering ceramics but also on geological, temperature-activated processes such as volcanic eruptions.     

Direct Characterization of Grain-Boundary Electrical Activity in Doped (Ba0.6Sr0.4)TiO3 by Combined Imaging of Electron-Beam-Induced Current and Electron-Backscattered Diffraction

Simultaneous measurements of remote electron beam induced current (REBIC) and orientation imaging microscopy (OIM) in a scanning electron microscope (SEM) have been applied to a polycrystalline (Ba_0.6Sr_0.4)TiO₃ with a positive temperature coefficient of resistivity (PTCR) to elucidate a grain-boundary character dependence of the potential barrier formation. The absence of electrical activity in a coherent Σ3 twin boundary is clearly imaged. The resistivity of individual grain boundaries estimated from a resistive contrast image is interpreted in terms of geometrical coherency, which is defined by the degree of coincidence in the reciprocal lattice points.     

Low-Frequency Measurements on the Grain-Boundary Internal Friction Peak in Chlorine-Doped Silicon Nitride

A procedure is shown to quantitatively analyze the morphology of the internal friction peak resulting from grain-boundary sliding. A Si₃N₄ polycrystal containing chlorine-doped SiO₂ at grain boundaries is selected as a model system for discussing chemical (e.g., anion) gradients at glassy grain boundaries. In this model material, grain boundaries lodging Cl⁻ anions show nonuniform thickness characteristics, which suggests a non-negligible dependence of the intergranular SiO₂-network structure upon grain misorientation. Both chemical and microstructural inhomogeneities existing in a polycrystalline ceramic body can result in peak broadening. The key for separating broadening contributions of chemical gradients from grain-size/morphology distributions resides in analyzing the peak-width change upon damping frequency. Groups of grain boundaries with different chemical characteristics may produce broadening because different peak components are generated that obey a spectrum of activation energies. On the other hand, microstructural inhomogeneities obey a single activation energy, but they generate a distribution of relaxation times. As a result, when a chemical gradient is present at grain boundaries, the peak may shift upon changing damping frequency with obeying a true activation energy, but its width increases with decreasing damping frequency. When peak broadening results only from microstructural inhomogeneities, the peak width is independent of damping frequency.     

Diffusion-Induced Grain-Boundary Migration in Ceria-Stabilized Tetragonal Zirconia Polycrystals

The microstructure and microchemistry of grain-boundary regions in (CeO₂+ La₂O₃)-stabilized tetragonal ZrO₂ polycrystals (Ce(La)-TZP) were studied by means of transmission electron microscopy (TEM). Evidence was found for the existence of crystalline and vitreous intergranular phases situated in small pockets at multiple grain junctions and in thin films along grain boundaries. In this ceramic system grain-boundary migration was observed in situ in the TEM in sample areas subjected to electron irradiation. Interfaces migrated away from their centers of curvature. Evidence was found for Ce de-alloying in the volume swept by the advancing boundaries. It is suggested that the coherency lattice strain brought about by a partial reduction of Ce, resulting in the diffusion of Ce³⁺ along grain boundaries to free surfaces, is the driving force for this phenomenon.     

Variation of Width and Composition of Grain-Boundary Film in a High-Purity Silicon Nitride with Minimal Silica

Contrary to the widely accepted observation that grain-boundary amorphous films for a given Si₃N₄ composition have common (equilibrium) widths and compositions, a significant variation for both parameters from film to film was observed in an undoped high-purity Si₃N₄ prepared using a hot isostatic pressing method. This material previously has been reported to have an equilibrium film width of 0.6 nm, as measured using a high-resolution electron microscopy (HREM) method; this value is significantly different from that which is typical for other high-purity Si₃N₄ ceramics (1.0 nm). A total of four boundaries were analyzed, using spatially resolved electron energy-loss spectroscopy methods, which can give the chemical width and composition for the film. Widths of these grain-boundary films were substantially different from each other; only the thinnest matches the previous HREM observations. The nitrogen content in the film decreased concurrently as the film thickened. This material had many cavities and complicated configurations at triple pockets, because of the very low total-SiO₂ content (0.55 vol%). They created locally different equilibrium conditions for grain-boundary films, in comparison with other fully densified Si₃N₄, causing such strong variation in both film structure and chemistry. This observation reveals the importance of triple pockets in equilibrium film structures, providing new insight in evaluating the absorption and wetting models. The thinnest film may correspond to the amorphous structure that is required to bind two randomly oriented Si₃N₄ grains under greater local stress.     

Forces between Aluminum Oxide Grains in a Silicate Melt and Their Effect on Grain Boundary Wetting

Experiments in which the disperson and flocculation behavior of aluminum oxide grains in a Ca-Al-Si-O silicate liquid are examined have been used to determine the nature of the forces between oxide grains in a silicate melt. From observations of the way in which the melt penetrates grain boundaries in a high-purity polycrystalline aluminum oxide, it is concluded that at short ranges the interaction between most grains is strongly repulsive. The formation of aggregated groups of grains in settling experiments, however, indicates that at larger separations the forces between grains become attractive and hence that there is an energetic minimum in the interaction between grains. The results are discussed in relation to models for the stability of intergranular films in liquid-phase-sintered ceramics. Microstructural observations made on the melt-penetrated aluminas are used to make a quantitative estimate of the fraction of grain boundaries that are wetted by the melt. The observations indicate that large clusters of grains connected by unwetted grain boundaries exist in liquid-phase-sintered aluminas.     

Nondestructive characterization of grain boundary Z-directional lateral surface in ZnO using nanorobot combined with SEM

Different from focusing on grain boundary upper surface in plane X–Y, a unique approach of nanorobot-based nondestructive characterization of grain boundary Z-directional lateral surface within bulk ZnO ceramic can be creatively developed under scanning electron microscope (SEM). By rolling-over bulk ZnO, two-dimensional profiles and grain boundaries in Z-directional lateral surfaces have been imaged in plane Y–Z and individually electrically characterized nondestructively. Experiments demonstrate that it is feasible to realize nondestructive characterization of grain boundary Z-directional lateral surface structures and electrical properties using nanorobot combined with SEM. Relative height differences between grain boundaries within Z-directional lateral surface can characterize the relative position relationships. Z-directional lateral surface structures can further extend irregular grain boundary lengths in plane Y–Z to interpret surface effects of nonlinear electrical properties. Relative minor electrical reactive effects in grain indicate grain boundary dominate in nonlinear macroscopic electrical properties. Furtherly, it can be advanced to promote a nondestructive characterization of grain boundary.     

Habits of Grains in Dense Polycrystalline Solids

We show here that the boundaries of individual grains in dense polycrystals prefer certain crystallographic habit planes, almost as if they were independent of the neighboring crystals. In MgO, SrTiO₃, MgAl₂O₄, TiO₂, and aluminum, the specific habit planes within the polycrystal correspond to the same planes that dominate the external growth forms and equilibrium shapes of isolated crystals of the same phase. The observations decrease the apparent complexity of interfacial networks and suggest that the mechanisms of solid-state grain growth may be analogous to conventional crystal growth. The results also indicate that a model for grain-boundary energy and structure based on grain surface relationships is more appropriate than the widely accepted models based on lattice orientation relationships.     

Formation of Potential Barrier Related to Grain-Boundary Character in Semiconducting Barium Titanate

Resistance–temperature ( R – T ) characteristics were measured directly at single-grain boundaries in 0.1-mol%-niobium-doped barium titanate bicrystals that had been fabricated from polycrystalline sinters, to determine a geometrical grain-boundary character dependence of the positive temperature coefficient of resistivity (PTCR) effect. Both random boundaries and low-Σ boundaries exhibit a similar grain-boundary character dependence of the PTCR effect through a simple geometrical analysis, using the coincidence of reciprocal lattice points. Differences of the R – T characteristics in individual boundaries have been explained in terms of the formation of a potential barrier that is associated with the oxidation of grain boundaries during cooling, after sintering or annealing. The grain-boundary character is likely to affect the diffusivity of O²⁻ ions and, hence, is crucial to the formation of the potential barrier.     

Microstructural and Chemical Influences of Silicate Grain-Boundary Phases in Yttria-Stabilized Zirconia

The microstructure and chemistry of grain-boundary phases in silicate-doped Y₂O₃─ZrO₂ ceramics were evaluated by analytical electron microscopy. Two different silicate compositions were used: one an aluminosilicate and the other a borosilicate glass. These grain-boundary phases had a significant impact on the grain morphology, the chemical composition of the grains, and the crystallization of second phases. These results indicate that controlled additions of specific glass phases may provide a means for tailoring the microstructure and physical properties of zirconia ceramics.     

Grain-Boundary and Grain Electrical Resistances in CoxFe3−xO4

The complex impedance analysis technique was used to separate the grain-boundary and grain impedances of ferrites of the system Co_xFe_3−xO₄. All the samples, for x = 0.886, 0.960, 0.980, 0.995, 0.999, 1.005, 1.011, 1.021, 1.041, and 1.126, were fabricated by the traditional routine under the same conditions of preparation and sintering. The variations of both grain-boundary and grain resistances with temperature were evaluated in the frequency range 100 Hz < f < 40 MHz. The values of the activation energies for both conduction processes were determined from the Arrhenius plots, and the variations of these activation energies and of the resistances at 20° and 150°C were drawn as a function of x. A sharp change in these quantities was observed at the stoichiometric composition (x = 1). Explanations and suggestions for the observed behaviors have been made.     

Grain-Boundary Chemistry of Barium Titanate and Strontium Titanate: II, Origin of Electrical Barriers in Positive-Temperature-Coefficient Thermistors

Scanning transmission electron microscopy (STEM) of positive-temperature-coefficient (PTC) BaTiO₃ thermistors shows that the grain-boundary oxygen content in as-received (oxidatively cooled) materials is slightly enriched compared to quenched samples, and the acceptor-rich space-charge present at high temperatures is retained upon cooling. The defect density of the space charge is approximately equal to the acceptor state density at PTC boundaries determined by electrical measurements. Accordingly, it is proposed that the electrical barrier forms when acceptor defects already segregated in the ionic space charge at high temperature become active interface states when compensating donor defects in the grain-boundary core are oxidized. These acceptor defects appear to be primarily barium vacancies, but need not form upon cooling in the manner proposed by Daniels and Wernicke. Acceptor solutes when present can also contribute to barrier formation through space-charge segregation; the increase in interface state density upon addition of Mn is consistent with the magnitude of the expected segregation.     

Microstructural evolution,non‐Ohmic properties,and giant dielectric response in CaCu3Ti4−xGexO12 ceramics

The microstructural evolution, non‐Ohmic properties, and giant dielectric properties of CaCu₃Ti_4?xGe_xO₁₂ ceramics (x=0‐0.10) are systematically investigated. The Rietveld refinement confirms the existence of a pure CaCu₃Ti₄O₁₂ phase in all samples. Significantly enlarged grain sizes of CaCu₃Ti_4?xGe_xO₁₂ ceramics are associated with the liquid phase sintering mechanism. Enhanced dielectric permittivity from 6.90×10⁴ to 1.08×10⁵ can be achieved by increasing Ge⁴⁺ dopant from x=0‐0.10, whereas the loss tangent is remarkably reduced by a factor of ≈10. Non‐Ohmic properties are enhanced by Ge⁴⁺ doping ions. Using impedance and admittance spectroscopies, the underlying mechanisms for the dielectric and nonlinear properties are well described. The improved nonlinear properties and reduced loss tangent are attributed to the enhanced resistance and conduction activation energy of the grain boundaries. The largely enhanced permittivity is closely associated with the enlarged grain sizes and the increase in the Cu⁺/Cu²⁺ and Ti³⁺/Ti⁴⁺ ratios, which are calculated from the X‐ray absorption near‐edge structure.     

Comparison of Sample Preparation and Analysis Using Solid-Phase Extraction and Solid-Phase Microextraction to Determine Monohydroxy PAH in Urine by GC/HRMS

Sample preparation techniques using solid-phase extraction (SPE) and solid-phase microextraction (SPME) are compared for the analysis of monohydroxy polycyclic aromatic hydrocarbons (OHPAH) in human urine. Urine samples spiked with five carbon-13 labeled internal standards are first enzymatically hydrolyzed. Sixteen OHPAH from eight parent compounds (naphthalene, fluorene, phenanthrene, fluoranthene, pyrene, chrysene, benzo[ c ]phenanthrene, and benz[ a ]anthracene) are then extracted along with the internal standards by these two different techniques. The analytes are derivatized by a silylating reagent before final analysis. Final separation and detection are performed by temperature-programmed capillary gas chromatography (GC) and high-resolution mass spectrometry (HRMS). The two extraction techniques are compared for sample preparation time, cost, throughput, reinjection possibility, frequency of outliers, matrix interference, signal linearity, and method detection limit. SPE demonstrates major advantages over SPME for most of these aspects.     

The One-Dimensional Car Parking Problem and Its Application to the Distribution of Spacings between Matrix Cracks in Unidirectional Fiber-Reinforced Brittle Materials

Experimental observations of the spacings between cracks formed in the matrix in unidirectional fiber-reinforced brittle materials in a situation where a tensile stress is applied parallel to the lengths of the fibers, and where the fibers have a longer elongation to failure than the matrix, suggest that the distribution of crack spacings does not follow the one expected on the basis of a model where the matrix cracks at a well-defined single-valued stress. A simple model which is able to account for this apparent discrepancy between theory and experiment is developed and discussed.     

Comparison between microwave and conventional calcination techniques in regard to reactivity and morphology of co-precipitated BaTiO3 powder,and the electrical and energy storage properties of the sintered samples

Barium titanate (BaTiO₃) nanopowders were synthesized by an aqueous co-precipitation method followed by calcination. Either 2.45 GHz microwaves or conventional heating was used in order to investigate the impact of these techniques on the synthesis time, microstructure, and electrical properties of the materials. The heating temperatures ranged from 620 °C to 810 °C. X-ray diffraction (XRD) revealed pure BaTiO₃ formation by microwave heating in a noticeably shorter time (five minutes) compared to conventional heating (3 h). Field emission scanning electron microscopy (FESEM) results confirmed that the microwave process led to nanocube formation, whereas in the conventional procedure, the particles tended to form spherical shapes. To evaluate the electrical properties, the samples heated at 620 °C were conventionally sintered at 1280 °C, 1330 °C, and 1380 °C. Higher dielectric, piezoelectric, and ferroelectric properties and more energy-saving efficiency (ε_r=1012, tan δ=0.035 d₃₃=85 pC/N, p_r=6.2 µC/cm² and η=48% respectively) were achieved in the microwave-heated BaTiO₃ sintered at 1380 °C compared to the conventionally heated BaTiO₃ (ε_r=824, tan δ=0.030 d₃₃=75 pC/N, p_r=5 µC/cm² and η=27%) demonstrating that microwave calcination substantially affects the final electrical properties.