Neutron Diffraction Measurements of the Residual Stresses in Al2O3-ZrO2 (CeO2) Ceramic Composites

High-resolution neutron powder diffraction was used to study the residual stresses in Al₂O₃-ZrO₂ (12 mol% CeO₂) ceramic composites containing 10, 20, and 40 vol% ZrO₂ (CeO₂). The diffraction data were analyzed using the Rietveld structure refinement technique. The analysis shows that for all samples, the CeO₂-stabilized tetragonal ZrO₂ particles are in tension and the Al₂O₃ matrix is in compression. For both the ZrO₂ particles and the Al₂O₃ matrix, the average lattice strains are anisotropic and increase approximately linearly with a decrease in the corresponding phase content. It is shown that these features can be qualitatively understood by taking into consideration the thermal expansion mismatch between the ZrO₂ and Al₂O₃ grains. Also, for all composite samples, the diffraction peaks are broader than the instrumental resolution, indicating that the strains in these samples are inhomogeneous. From an analysis of the refined peak shape parameters, the average root-meansquare strain, which describes the distribution of the inhomogeneous strain field, was determined. Finally, the average residual stresses were evaluated from the experimentally determined average lattice strains and compared with recent results of X-ray measurements on similar composites.     

Protonic and electronic conductivity of the layered perovskite oxides HCa2Nb3O10 and Ca4Nb6O19

The structural and electrical properties of the Dion–Jacobson series layer perovskite HCa₂Nb₃O₁₀ were investigated. Within the intermediate temperature range (200–475 °C), the compound undergoes topochemical dehydration to Ca₄Nb₆O₁₉ and, under reducing atmospheres, partial reduction of Nb(V) to Nb(IV). These changes occur upon heating and are not reversed on cooling. Analysis of impedance data shows that the conductivity of Ca₄Nb₆O₁₉ is predominantly electronic under reducing atmospheres, consistent with the behavior of other structurally related mixed-valence layered niobates.     

Microstructure and Crystallography of Titanium Nitride Whiskers Grown by a Vapor–Liquid–Solid Process

Titanium nitride whiskers having diameters of 0.5 to 1.5 μm and aspect ratios in the range of 20 to 50 have been produced by a new commercially scalable vapor–liquid–solid process. Electron microscopy studies have shown that most of the whiskers can be classified into two types based upon structure and morphology. The whiskers of one type are single crystals and have a growth direction of (100). Whiskers of the second type are comprised of two crystals having a common (110) growth direction. Both types have smooth surfaces and relatively few internal defects. Additionally, a small percentage of whiskers have considerable internal structure related to significant magnesium impurities.     

丰城赣江大桥水上钻孔定位测量

丰城赣江大桥工程地质勘察水上钻孔定位施工放样是采用方向法前方交会.用电磁波测距三角高程测量来测定其孔口标高.从误差传播定律的角度,论证了该施测方案的正确性,同时也论述了要达到高精度放样的最佳图形是布设成两底角为锐角的等腰三角形.     

Semi‐Crystalline Polymer Blends for Material Extrusion Additive Manufacturing Printability: A Case Study with Poly(ethylene terephthalate) and Polypropylene

Semi‐crystalline polymers are an important class of materials for engineering applications due to their high modulus and barrier properties. Traditional manufacturing methods process semi‐crystalline polymers via rigid molds and well‐controlled temperature and pressure environments to handle the significant change in specific volume occurring during crystallization; however, material extrusion additive manufacturing does not use these features. This often leads to warpage‐induced build failure in fused filament fabrication (FFF). To enable FFF of semi‐crystalline polymers, this work investigates characteristics of immiscible polymer blends (e.g., disparate crystallization behavior and phase separation) to mitigate warping failure during printing. A series of poly(ethylene terephthalate)/polypropylene/polypropylene–graft–maleic anhydride blends are explored and the effect of thermal and morphological characteristics on printability is analyzed. It is shown that these blends can be extruded into filament and printed into a 3D structure. Extrapolations indicate that phase‐separated blends with increased total crystallization half‐time are beneficial for FFF printing.     

Crystallization of Precursors to Forsterite and Chromium-Doped Forsterite

The pyrolysis and crystallization of poly(methacrylate) precursors and xerogels of forsterite and chromium-doped forsterite were studied by in situ high-temperature, dynamic X-ray diffraction and thermal analysis. For both types of precursor, crystallization of forsterite occurred at lower temperature when doped with chromium. Also, exotherms above 700°C occurred 50°C lower when chromium was present. When residual carbon in the xerogels was more than ∼1%, an unidentified crystalline intermediate phase formed at ∼800°C. Conversion of the intermediate phase to forsterite was faster than amorphous material. Thus, full crystallinity was attained at a lower temperature when the xerogels had some residual carbon.     

Cubic-to-Tetragonal Displacive Transformation in Gd2O3–Bi2O3 Ceramics

Gd₂O₃-doped Bi₂O₃ polycrystalline ceramics containing between 2 and 7 mol% Gd₂O₃ were fabricated by pressureless sintering powder compacts. The as-sintered samples were tetragonal at room temperature. Hightemperature X-ray diffraction (XRD) traces showed that the samples were cubic at elevated temperatures and transformed into the tetragonal polymorph during cooling. On the basis of conductivity measurements as a function of temperature and differential scanning calorimetry (DSC), the cubic → tetragonal as well as tetragonal → cubic → teansition temperatures were determined as a function of Gd₂O₃ concentration. The cubic → tetragonal transformation appears to be a displacive transformation. It was observed that additions of ZrO₂ as a dopant, which is known to suppress cation interdiffusion in rare-earth oxide–Bi₂O₃ systems, did not suppress the transition, consistent with it being a displacive transition. Annealing of samples at temperatures 660°C for several hundred hours led to decomposition into a mixture of monoclinic and rhombohedral phases. This shows that the tetragonal polymorph is a metastable phase.     

Effect of Nb2O5 Alloying on Thermal Expansion Anisotropy of 2 mol% Y2O3-Stabilized Tetragonal ZrO2

Tetragonal ZrO₂ ( t -ZrO₂) solid solutions were prepared with addit ons of 2 mol% Y₂O₃ plus up to 0.45 mol% Nb₂O₅. The thermal expansion coefficients in both the a- and c -axis lattice directions increased with Nb₂O₅ alloying and the thermal expansion in the c -axis direction was greater than that in the a -axis direction over the entire composition range. This anisotropic thermal expansion behavior was related to the 4-fold coordination of Nb⁵⁺ with oxygen ions in t -ZrO₂ solid solutions in the system ZrO₂–Y₂O₃–Nb₂O₅. The fracture toughness continuously increased with Nb₂O₅ alloying and suggested that the c/a axial ratio is a more significant factor than the internal stress that arises from the thermal expansion anisotropy, in the determination of the transformability of t -ZrO₂ in this system.     

Surface-Bound Microgels for Separation,Sensing, and Biomedical Applications

This study presents a comprehensive survey of microgel-coated materials and their functional behavior, describing the complex interplay between the physicochemical and mechanical properties of the microgels and the chemical and morphological features of substrates. The cited literature is articulated in four main sections: i) properties of 2D and 3D substrates, ii) synthesis, modification, and characterization of the microgels, iii) deposition techniques and surface patterning, and iv) application of microgel-coated surfaces focusing on separations, sensing, and biomedical applications. Each section discusses – by way of principles and examples – how the various design parameters work in concert to deliver functionality to the composite systems. The case studies presented herein are viewed through a multi-scale lens. At the molecular level, the surface chemistry and the monomer make-up of the microgels endow responsiveness to environmental and artificial physical and chemical cues. At the micro-scale, the response effects shifts in size, mechanical, and optical properties, and affinity towards species in the surrounding liquid medium, ranging from small molecules to cells. These phenomena culminate at the macro-scale in measurable, reversible, and reproducible effects, aiming in a myriad of directions, from lab-scale to industrial applications.