An asymptotic maximum likelihood for estimating the nominal angle of a spatially distributed source

This paper proposes a large-sample approximation of the maximum-likelihood estimator for direction finding in the presence of a spatially spread source. The key idea is to replace the parametric estimate of the four-dimensional nuisance parameter vector with the approximate one that depends on just one parameter of interest, called the nominal angle, thus permitting the use of one-dimensional optimization techniques. The proposed estimator is shown to be strongly consistent and asymptotically efficient, and the Cramér–Rao bound on its standard deviation is derived. Simulations show the estimator to outperform previously proposed estimators, such as the subspace-based estimator and others based on one-dimensional search.     

Distribution of Elements in a Cu-Added FeSi<Subscript>2</Subscript> Alloy Under Peritectoid and Eutectoid Reactions

The distribution of Si, Fe, and Cu in FeSi₂ alloys, with or without the addition of Cu, were studied by electron probe microanalysis (EPMA). Alloys were prepared by slow solidification from the melt. Without Cu addition, both ε- and α-phases were clearly observed, and a β-phase surrounding the ε-phase was additionally observed after in situ annealing at 950°C for 12 h. With inclusion of 0.5 at.% Cu, the eutectoid reaction (α → β + Si) was enhanced greatly. Only 0.01 at.% Cu was dissolved into the ε-phase, with the excess Cu atoms being largely found at the outer edge of the ε-phase. Ex situ annealing at 950°C for 12 h greatly changed the distribution of Si, Fe, and Cu. The ε-phase changed its Si/Fe atomic ratio from 1.470 to 1.907, indicating an early stage of the peritectoid reaction (ε + α → β) and/or the subsequent reaction (ε + Si → β), with an increase in the Cu content up to 0.04 at.%. The size of this new phase was smaller than the original ε-phase, and this new phase was surrounded by a shell of Si/Fe with an atomic ratio of 0.727 to 1.788 and a Cu content of 0.01 at.% to 0.11 at.%. In situ annealing under the same condition yielded different results: a large amount of Si segregates from the α-phase matrix, leaving a Si/Fe atomic ratio of only 0.506 to 0.530. The peritectoid reaction of the ε-phase was found to depend on the Cu content. For the ε-phase with undetectable levels of Cu, the Si/Fe atomic ratio remained at 0.954 to 0.998, but this ratio decreased with increasing Cu content to 0.55 at 2.20 at.% Cu. A plot of at.% Cu versus Si/Fe atomic ratio revealed a local minimum at the ε-phase and expectedly at both the β- and α-phases. Nonstoichiometric structures (neither α-, β- nor ε-phases) seemed to have higher at.% Cu compared with those with the closest Si/Fe composition.     

Development of high 1-deoxynojirimycin (DNJ) content mulberry tea and use of response surface methodology to optimize tea-making conditions for highest DNJ extraction

Mulberry 1-deoxynojirimycin (DNJ), a potent α-glucosidase inhibitor, suppresses postprandial blood glucose, thereby possibly preventing diabetes mellitus. At present, mulberry dry teas are commercially supplied as functional foods in many countries, but these products may not provide an effective dose (6 mg DNJ/60 kg human wt) due to their low DNJ content (about 100 mg/100 g of dry wt). Therefore, development of tea with higher DNJ content is desirable. To do this, we investigated distribution of DNJ content and α-glucosidase inhibitory activity in 35 Thai mulberry varieties. DNJ content in young leaves varied among mulberry varieties from 30 to 170 mg/100 g of dry leaves. Varieties having highest DNJ content were Kam, Burirum 60 and Burirum 51. Leaf position affected DNJ content: shoots > young leaves > mature leaves. DNJ concentration and α-glucosidase inhibitory activity were highly correlated (r = 0.84), suggesting that α-glucosidase inhibitory activity of mulberry leaves is mainly due to DNJ. Consequently, high DNJ content mulberry tea was produced from shoots of varieties such as Burirum 60, which contains 300 mg/100 g of dry wt. Tea-making conditions were optimized for highest DNJ extraction using response surface methodology. Approximate 95% of total DNJ in high DNJ content dry tea was extracted when temperature was maintained at 98 °C for 400 s; these conditions could be applicable for preparation of commercial products with high DNJ content. One cup (230 ml, a normal serving) of DNJ-enriched mulberry tea contained enough DNJ (6.5 mg) to effectively suppress postprandial blood glucose.     

Morphology development of ZnO produced by sonothermal process

Wurtzite ZnO (hcp) was produced by the 80 °C sonothermal reactions of 1:5, 1:10, and 1:20 molar ratios of Zn(NO₃)₂·6H₂O:NaOH in water, containing 2 g, 5 g, 10 g, and 20 g of polyethylene glycol (PEG) with the molecular weights (MWs) of 6000, 10000, and 20000 for 1 h, 3 h, and 5 h. ZnO phase with different morphologies was detected. When the amount of NaOH, both MW and the amount of PEG, and the experimental time were increased, the products still retain their single phase, but their morphologies were changed from nanoplates in clusters to nanospears with sharp tips gathering together in the shape of flowers, and long nanorods with oval tips in clusters. In the present work, formation mechanism of these products was also discussed.     

Large-scale synthesis of WO3 nanoplates by a microwave-hydrothermal method

Tungsten oxide (WO₃) nanoplates were synthesized by a 270 W microwave-hydrothermal reaction of Na₂WO₄·2H₂O and citric acid (C₆H₈O₇·H₂O) in deionized water. X-ray diffraction (XRD), scanning electron microscopy (SEM), high resolution transmission electron microscopy (HRTEM), and selected area electron diffraction (SAED) were used to reveal the synthesis of WO₃ complete rectangular nanoplates in the solution of 0.2 g citric acid for 180 min, with O-W-O FTIR stretching modes at 819 and 741 cm⁻¹, and two prominent O-W-O Raman stretching modes at 804 and 713 cm⁻¹. The 2.71 eV indirect energy gap, and 430-460 nm blue emission wavelength range of WO₃ complete rectangular nanoplates were determined using UV-visible and photoluminescence (PL) spectrometers. The formation mechanism was also proposed according to the experimental results.     

Oxidative Stress and Its Significant Roles in Neurodegenerative Diseases and Cancer

Reactive oxygen and nitrogen species have been implicated in diverse pathophysiological conditions, including inflammation, neurodegenerative diseases and cancer. Accumulating evidence indicates that oxidative damage to biomolecules including lipids, proteins and DNA, contributes to these diseases. Previous studies suggest roles of lipid peroxidation and oxysterols in the development of neurodegenerative diseases and inflammation-related cancer. Our recent studies identifying and characterizing carbonylated proteins reveal oxidative damage to heat shock proteins in neurodegenerative disease models and inflammation-related cancer, suggesting dysfunction in their antioxidative properties. In neurodegenerative diseases, DNA damage may not only play a role in the induction of apoptosis, but also may inhibit cellular division via telomere shortening. Immunohistochemical analyses showed co-localization of oxidative/nitrative DNA lesions and stemness markers in the cells of inflammation-related cancers. Here, we review oxidative stress and its significant roles in neurodegenerative diseases and cancer.     

Transformation of cubic AgBiS2 from nanoparticles to nanostructured flowers by a microwave-refluxing method

Cubic AgBiS₂ nanoparticles and flower-like clusters were successfully synthesized by microwave refluxing of CH₃COOAg, Bi(NO₃)₃·5H₂O and thiosemicarbazide (NH₂NHCSNH₂) in ethylene glycol. The phase was detected by X-ray diffraction (XRD) and selected area electron diffraction (SAED). The SAED pattern was also in accordance with that of the simulation. Scanning and transmission electron microscopy (SEM and TEM) revealed the gradual transformation of nanoparticles into flower-like clusters by increasing microwave power. Their UV–visible absorption and photoluminescence (PL) emission were detected by spectrometry. Possible formation mechanism of nanoparticles and nanostructured flowers was also proposed according to the experimental results.     

Biomolecule and surfactant-assisted hydrothermal synthesis of PbS crystals

PbS crystals were hydrothermally synthesized using Pb(NO₃)₂, l-cysteine, and N-cetyl pyridinium chloride in solutions with different pH values at 140 °C. Flower-like, granular and truncated cubic PbS crystals composing of Pb and S were detected using an X-ray diffractometer (XRD), a scanning electron microscope (SEM), a transmission electron microscope (TEM), a selected area electron diffraction (SAED) technique and an energy dispersive X-ray (EDX) analyzer. In addition, a Raman spectrometer revealed the presence of the first and second overtone modes at 436 and 602 cm⁻¹, respectively. Emission spectra of the products were detected at 412 nm using a photoluminescence (PL) spectrometer.     

Solid-state synthesis of cubic ZnTe nanocrystals using a microwave plasma

Cubic ZnTe nanocrystals were produced from 1:1 and 1.8:1 molar ratios of Zn:Te by a 900 W microwave plasma. The phase was detected using X-ray diffraction (XRD), which are in accordance with those of the simulations, and selected area electron diffraction (SAED). Raman spectroscopy, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) showed that the products were nanocrystals with different orientations, including three longitudinal optical (LO) vibrations at 205, 410 and 620 cm^? 1 and a transverse optical (TO) vibration at 166 cm^? 1. Their green emissions were detected at 562 nm (2.21 eV) using luminescence spectrophotometry.     

Transient solid-state production of nanostructured CuS flowers

CuS (hcp) with different morphologies was produced using a transient solid-state reaction by the direct flow of electricity through solids, containing 1:1 molar ratio of Cu:S powders, in a high vacuum system for different lengths of time. X-ray diffraction (XRD), selected area electron diffraction (SAED), and scanning and transmission electron microscopies (SEM and TEM) specified that the products were nanostructured CuS flowers, and nanostructured CuS composing of nanoparticles with different orientations, controlled by the length of time. Raman vibrations were detected at 474.5 cm^− 1, and photoluminescent (PL) emissions at 347.5 nm. Both the XRD and SAED patterns are in accordance with those obtained by the corresponding simulations.