Preparation of Aluminum Nitride Powder from Aluminum Polynuclear Complexes

AIN powder was synthesized from aluminum polynuclear complexes. Basic aluminum chloride and basic aluminum lactate were used as the aluminum polynuclear complexes. These starting materials and glucose were dissolved in water and mixed homogeneously. AIN powder was obtained by calcining after drying and precalcining at 800°C under nitrogen gas flow. Then excess carbon was removed by firing in air. Nitridation in the system was investigated and compared with that in the alumina–carbon black system. It was found that in our reaction system nitridation began and proceeded at lower calcination temperatures above 1200°C than in the alumina–carbon black system. Using aluminum polynuclear complexes, AIN was synthesized through the nitridation of γ-alumina and produced in a very fine and sharp particle size distribution.     

Effect of Nd2O3 Concentration on the Defect Structure of CeO2–Nd2O3 Solid Solution

An extensive X-ray study of CeO₂–Nd₂O₃ solid solutions was performed, and the densities of solid solutions containing various concentrations of NdO_1.5 were measured using several techniques. Solid solutions containing 0–80 mol% NdO_1.5 were synthesized by coprecipitation from Ce(NO₃)₃ and Nd(NO₃)₃ aqueous solutions, and the coprecipitated samples were sintered at 1400°C. A fluorite structure was observed for CeO₂–NdO_1.5 solid solutions with 0–40 mol% NdO_1.5, which changed to a rare earth C-type structure at 45–75 mol% NdO_1.5. The change in the lattice parameters of CeO₂–NdO_1.5 solid solutions, when plotted with respect to the NdO_1.5 concentration, showed that the lattice parameters followed Vegard's law in both the fluorite and rare earth C-type regions. The maximum solubility limit for NdO_1.5 in CeO₂ solid solution was approximately 75 mol%. The relationship between the density and the Nd concentration indicated that the defect structure followed the anion vacancy model over the entire range (0–70 mol% NdO_1.5) of solid solution.     

Some properties of Sb2Te3−xSex for nonvolatile memory based on phase transition

Composition dependence of properties of Sb₂Te_3–x Se _x in the range 0x<3 were studied using differential thermal analysis and X-ray diffraction. Sb₂Te_3–x Se _x form solid solution for 0<x1.25 and 2.75x<3. A systematic study of crystallization temperature in Sb₂Te_3–x Se _x (0x2.75) thin films prepared by flash evaporation was carried out. In preliminary experiments for some compositions, more than 10³ repetitions between amorphous and crystalline states were attained by the application of electric pulses.     

Inside Front Cover: Self‐Assembly of SiO2 Nanowires and Si Microwires into Hierarchical Heterostructures on a Large Scale (Adv. Mater. 8/2005)

The inside cover shows a scanning electron micrograph of a novel hierarchical heterostructures, as reported by Hu and co‐workers on p. 971. The heterostructures are formed from Si core microwires covered by dense, aligned SiO₂ nanowires, thus forming multiple junctions to the cores. The inset shows a schematic of the Sn‐catalyzed vapor–liquid–solid growth mechanism. These materials are envisaged to become important for optical fibers, low‐dimensional waveguides, scanning near‐field optical microscopes and high‐bandwidth optical signal processing devices.     

Inside Front Cover: Self‐Assembled Highly Faceted Wurtzite‐Type ZnS Single‐Crystalline Nanotubes with Hexagonal Cross‐Sections (Adv. Mater. 16/2005)

Highly faceted wurtzite‐type ZnS nanotubes with hexagonal cross‐section morphologies have been self‐assembled via a controllable high‐temperature thermal‐chemical reaction route in work reported by Yin and co‐workers on p. 1972. The self‐assembly growth along c‐axis to highly hexagonal‐faceted ZnS single‐crystalline nanotubes is associated with the crystallographic characteristics, such as the non‐central and polar surfaces of the wurtzite‐type ZnS structure. The faceted ZnS nanotubes grow along the <0001> direction, and are closed by low‐index faces of non‐polar {1000} faces. The inside cover and insets show electron microscopy and scanning electron microscopy images of the faceted ZnS nanotubes.     

Effect of Platelet-Rich Plasma on M1/M2 Macrophage Polarization

Osteoarthritis of the knee (OAK) is a chronic degenerative disease and progresses with an imbalance of cytokines and macrophages in the joint. Studies regarding the use of platelet-rich plasma (PRP) as a point-of-care treatment for OAK have reported on its effect on tissue repair and suppression of inflammation but few have reported on its effect on macrophages and macrophage polarization. Based on our clinical experience with two types of PRP kits Cellaid Serum Collection Set P type kit (leukocyte-poor-PRP) and an Autologous Protein Solution kit (APS leukocyte-rich-PRP), we investigated the concentrations of humoral factors in PRPs prepared from the two kits and the effect of humoral factors on macrophage phenotypes. We found that the concentrations of cell components and humoral factors differed between PRPs purified using the two kits; APS had a higher concentration of M1 and M2 macrophage related factors. The addition of PRP supernatants to the culture media of monocyte-derived macrophages and M1 polarized macrophages revealed that PRPs suppressed M1 macrophage polarization and promoted M2 macrophage polarization. This research is the first to report the effect of PRPs purified using commercial kits on macrophage polarization.     

Dynamic Stabilization of DNA Assembly by Using Pyrrole-Imidazole Polyamide

We used N-methylpyrrole (Py)-N-methylimidazole-(Im) polyamide as an exogenous agent to modulate the formation of DNA assemblies at specific double-stranded sequences. The concept was demonstrated on the hybridization chain reaction that forms linear DNA. Through a series of melting curve analyses, we demonstrated that the binding of Py−Im polyamide positively influenced both the HCR initiation and elongation steps. In particular, Py−Im polyamide was found to drastically stabilize the DNA duplex such that its thermal stability approached that of an equivalent hairpin structure. Also, the polyamide served as an anchor between hairpin pairs in the HCR assembly, thus improving the originally weak interstrand stability. We hope that these proof-of-concept results can inspire future use of Py−Im polyamide as a molecular tool to modulate the formation of DNA assemblies.