Kinetics of Templated Grain Growth of 0.65Pb(Mg1/3Nb2/3)O3·0.35PbTiO3

Single-crystal layers of 0.65Pb(Mg_1/3Nb_2/3)O₃·0.35PbTiO₃ (PMN-35PT) were grown heteroepitaxially on {001}-BaTiO₃ template crystals. A {001}-BaTiO₃ crystal was embedded in a fine-grained matrix of PMN-35PT containing excess PbO and heated between 950° and 1150°C for 0–5 h. The initial growth of the PMN-35PT on the {001} surface and the growth of the matrix grains both displayed a t ^1/3 dependence which is characteristic of diffusion-controlled growth. Growth was limited to ∼100–150 μm due to the significantly reduced driving force at longer times because of matrix coarsening and porosity evolution.     

The role of ceramic and glass science research in meeting societal challenges: Report from an NSF‐sponsored workshop

Under the sponsorship of the U.S. National Science Foundation, a workshop on emerging research opportunities in ceramic and glass science was held in September 2016. Reported here are proceedings of the workshop. The report details eight challenges identified through workshop discussions: Ceramic processing: Programmable design and assembly; The defect genome: Understanding, characterizing, and predicting defects across time and length scales; Functionalizing defects for unprecedented properties; Ceramic flatlands: Defining structure‐property relations in free‐standing, supported, and confined two‐dimensional ceramics; Ceramics in the extreme: Discovery and design strategies; Ceramics in the extreme: Behavior of multimaterial systems; Understanding and exploiting glasses and melts under extreme conditions; and Rational design of functional glasses guided by predictive modeling. It is anticipated that these challenges, once met, will promote basic understanding and ultimately enable advancements within multiple sectors, including energy, environment, manufacturing, security, and health care.     

Predicting the deposition spot radius and the nanoparticle concentration distribution in an electrostatic precipitator

Abstract

Deposition of aerosol nanoparticles using an electrostatic precipitator is widely used in the aerosol community. Despite this, basic knowledge regarding what governs the deposition has been missing. This concerns the prediction of the size of the particle collection zone, but also, perhaps more importantly, prediction of the nanoparticle concentration distribution on the substrate, both of which are necessary to achieve faster and more precise deposition. In this article, we have used COMSOL Multiphysics simulations, experimental depositions, and two analytical models to describe the deposition. Based on that, we propose a simple equation that can be used to predict the size of the deposition spot as well as the particle concentration on the substrate. The equation we derive concludes that the size of the deposition spot only depends on the gas flow rate into the precipitator, and on the constant drift velocity of a particle in an electric field. The equation also displays that the deposited particle concentration is independent of the gas flow rate. Our general mathematical analysis has great applicability, as it can be used to model different geometries and different types of deposition methods than the one described in this article. We can therefore also propose that the drift velocity in this model easily could be replaced by another velocity acting on the particles at other deposition conditions, for instance, the thermophoretic velocity during thermophoretic deposition. This would result in the same dependence as presented in this article. Finally, we demonstrate analytically and through experiment that the particle distribution inside the spot will be homogenous and follows a top hat profile.     

Bladder Cancer Extracellular Vesicles Elicit a CD8 T Cell-Mediated Antitumor Immunity

Tumor-derived extracellular vesicles (TEVs) play crucial roles in mediating immune responses, as they carry and present functional MHC-peptide complexes that enable them to modulate antigen-specific CD8⁺ T-cell responses. However, the therapeutic potential and immunogenicity of TEV-based therapies against bladder cancer (BC) have not yet been tested. Here, we demonstrated that priming with immunogenic Extracellular Vesicles (EVs) derived from murine MB49 BC cells was sufficient to prevent MB49 tumor growth in mice. Importantly, antibody-mediated CD8⁺ T-cell depletion diminished the protective effect of MB49 EVs, suggesting that MB49 EVs elicit cytotoxic CD8⁺ T-cell-mediated protection against MB49 tumor growth. Such antitumor activity may be augmented by TEV-enhanced immune cell infiltration into the tumors. Interestingly, MB49 EV priming was unable to completely prevent, but significantly delayed, unrelated syngeneic murine colon MC-38 tumor growth. Cytokine array analyses revealed that MB49 EVs were enriched with pro-inflammatory factors that might contribute to increasing tumor-infiltrating immune cells in EV-primed MC-38 tumors. These results support the potential application of TEVs in personalized medicine, and open new avenues for the development of adjuvant therapies based on patient-derived EVs aimed at preventing disease progression.     

Improved Fracture Behavior of Alumina Microstructural Composites with Highly Textured Compressive Layers

Alumina‐based microstructural composites combining equiaxed and textured layers were fabricated to examine how cracks propagate and the mechanical properties are affected as a function of the residual stress and volume fraction of texture in a multilayer structure. By combining equiaxed and highly textured alumina layers of varying thermal expansion, the embedded textured layers were placed under compressive residual stresses as high as ?670 MPa. Composites with a near constant maximum failure stress of up to 300 MPa were shown to be almost independent of the initial defect size as result of the compressive residual stress in the textured layers. An apparent fracture toughness of up to 10.1 MPa·m^1/2 was obtained for composites with an equiaxed to textured volume ratio of 7.4:1. The high compressive stress in the textured layers arrested cracks, whereas the weak bonding parallel to the basal surfaces of the textured alumina grains caused cracks to deflect within the textured layers. The coupling of these two mechanisms resulted in crack arrest and a maximum work of fracture of ~1200 J/m² or almost 50 times higher than equiaxed alumina. We believe that embedding textured layers having compressive stresses below the surface of multilayer composites represent an important strategy for designing flaw‐tolerant materials with pronounced crack growth resistance and a high work of fracture.     

Fabrication and Electrical Properties of Textured Sr0.53Ba0.47Nb2O6 Ceramics by Templated Grain Growth

Textured Sr_0.53Ba_0.47Nb₂O₆ ceramics with a relative density of >95% were fabricated using templated grain growth (TGG). Acicular KSr₂Nb₅O₁₅ template particles synthesized via a molten salt process were aligned by tape casting in a mixture of solid-state-synthesized SrNb₂O₆ and BaNb₂O₆ powders. The resulting ceramics possessed strong fiber texture along the polar axis ([001]) of the strontium barium niobate. Samples with 15.4 wt% templates attained a textured fraction of 0.82 after sintering at a temperature of 1450°C for 4 h. These materials showed peak dielectric constants of 7550 at 1 kHz, remanent polarizations of 13.2 μC/cm², saturation polarizations of 21 μC/cm² (60%–85% of the single-crystal value), piezoelectric strain coefficients of 78 pC/N (70%–85% of the single-crystal value), and room-temperature pyroelectric coefficients of 2.9 × 10⁻²μC·(cm²·°C)⁻¹ (52% of the single-crystal value). These results show that TGG is a viable option for accessing single-crystal properties in polycrystalline ceramics.     

Gas Diffusion During Containerless Hot Isostatic Pressing of Liquid-Phase Sintered Ceramics

Diffusion and dissolution of gases are considerably higher in glasses than in most crystalline materials. Thus, materials with a glassy grain-boundary phase are susceptible to gas permeation when they are containerless hot isostatic pressed. Annealing of sinter-hot isostatic pressed alumina—magnesium aluminosilicate glass (3 to 10 vol%) composites and pure glass samples at 1200° to 1600°C results in dedensification by matrix bloating and swelling. The degree of dedensification increases with the hot isostatic pressing pressure, temperature, and time and increasing annealing temperature. A theoretical prediction of high-pressure gas permeation is developed based on a diffusion model. The analysis allows a satisfactory explanation for the gas diffusion effect on hot isostatic press densification. The analysis is also useful for developing design criteria for the hot isostatic press schedule and encapsulation materials. Annealing of hot isostatic pressed samples at 1100°C prior to high-temperature annealing results in no dedensification as a result of out-diffusion of the internal gases.     

Simultaneous growth mechanisms for Cu-seeded InP nanowires

We report on epitaxial growth of InP nanowires (NWs) from Cu seed particles by metal-organic vapor phase epitaxy (MOVPE). Vertically-aligned straight nanowires can be achieved in a limited temperature range between 340 °C and 370 °C as reported earlier. In this paper we present the effect of the V/III ratio on nanowire morphology, growth rate, and particle configuration at a growth temperature of 350 °C. Two regimes can be observed in the investigated range of molar fractions. At high V/III ratios nanowires grow from a solid Cu₂In particle. At low V/III ratios, nanowire growth from two particle types occurs simultaneously: Growth from solid Cu₂In particles, and significantly faster growth from In-rich particles. We discuss a possible growth mechanism relying on a dynamic interplay between vapor-liquid-solid (VLS) and vapor-solid-solid (VSS) growth. Our results bring us one step closer to the replacement of Au as seed particle material as well as towards a deeper understanding of particle-assisted nanowire growth.      

The Reaction-Bonded Aluminum Oxide (RBAO) Process: II, The Solid-State Oxidation of RBAO Compacts

The oxidation kinetics and the fraction of aluminum that is oxidized via solid–gas reaction in reaction-bonded aluminum oxide (RBAO) compacts are shown to be strongly dependent on the oxidation temperature and the characteristics (size and green density) of the RBAO compact. Based on the Biot number, the oxidation process of RBAO compacts is controlled by convective heat transfer. Low heat transfer from the surface of the compact results in too-rapid oxidation, thermal gradients, and core–shell oxidation of the compacts. Uniform oxidation of RBAO compacts is possible by oxidizing at low temperatures (400°–470°C), where slow surface reaction of the aluminum particles controls the oxidation of the compact. A grain model is presented to cover both linear and nonlinear oxidation regimes during the oxidation of a RBAO compact, and this model predicts the experimental results when surface reaction of the aluminum particles is the rate-controlling mechanism and oxidation of the compact occurs uniformly.     

Processing and Microstructure Development in Alumina–Silicon Carbide Intragranular Particulate Composites

Al₂O₃–SiC particulate composites were fabricated by hot-pressing mixtures of 5–30 vol% SiC with either α-Al₂O₃, γ-Al₂O₃, or boehmite (γ-AlOOH) to determine whether grain growth or the α-alumina phase transformation could be used to fabricate intragranular particulate composites. Samples starting with α-alumina resulted in primarily intergranular SiC of 0.3 μ and an alumina grain size of 1.5–4.1 μm. Heat treatments resulted in SiC coarsening but no entrapment of SiC by grain boundary breakaway. The α-alumina transformation in the samples starting with γ-alumina resulted in the entrapment of ∼48% of the 5 vol% of SiC added whereas 79% of the SiC was entrapped in the α-alumina grains in samples starting with boehmite. Only SiC particles ≤0.2 SmUm were entrapped in the α-alumina grains during the phase transformation. With increasing SiC content, the relative volume of intragranular SiC decreased, but the amount of intragranular SiC was constant and independent of the amount of SiC added before transformation. The formation of intragranular composites from γ-alumina and boehmite samples was explained with a model that attributes particle entrapment to the vermicular growth of α-alumina into the transition alumina matrix during the α-alumina phase transformation. Seeding the boehmite-based samples did not affect the concentration of entrapped SiC, but did lower the hot-pressing densification temperature by as much as 150°C.