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Pre-spray-drying processing may affect stability after reconstitution of emulsion-based powders, such as infant formulas. This study aimed to evaluate the effects of pasteurization temperature and total solids (TS) of the feed on the stability of the emulsions obtained from the reconstituted powders. Four infant formula powders (50%-75 °C, 50%-100 °C, 60%-75 °C, and 60%-100 °C) were produced at pilot scale, from emulsions with 50 or 60% TS pasteurized at 75 or 100 °C for 18 s. Both the emulsion feeds and the emulsions from the reconstituted powders (12.5% TS) were analyzed. The results showed that feeds with 60% TS were flocculated, as indicated by the large particle size and viscosity and the pseudoplastic behavior. Light microscopy revealed that, during spray drying, the flocs were disrupted in 60%-100 °C, while the 60%-75 °C emulsion remained flocculated, reducing its stability post-reconstitution. Although all four emulsions were mainly stabilized by caseins, the presence of ß-lactoglobulin was also detected at the oil-water interface, in native state in the formulas preheated at 75 °C and aggregated in the formulas preheated at 100 °C. In conclusion, both the degree of whey protein denaturation (resulting from pasteurization) and the TS of the concentrates during infant formula production affected the emulsion stability of the reconstituted powders.

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This work proposes the slope of the phase spectrum as a signal processing parameter for the ultrasonic monitoring of the water content of water-in-crude oil emulsions. Experimental measurements, with water volume fractions from 0 to 0.48 and test temperatures of 20 °C, 25 °C, and 30 °C, were carried out using ultrasonic measurement devices operating in transmission-reception and backscattering modes. The results show the phase slope depends on the water volume fraction and, to a lesser extent, on the size of the emulsion droplets, leading to a stable behavior over time. Conversely, the behavior of the phase slope as a function of the volume fraction is monotonic with low dispersion. Fitting a power function to the experimental data provides calibration curves that can be used to determine the water content with percentage relative error up to 70% for a water volume fraction of 0.06, but less than 10% for water volume fractions greater than 0.06. Furthermore, the methodology works over a wide range of volume fractions.

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Kinematic indicators, including certain strain fringes, represent an important group of structures related to the progressive deformation in rocks. The evolution of these fibrous textures can be explained by the combination of multiple mechanisms of deformation and fluid flow, mainly controlled by the orientation of the strain field and the morphology of the grains. In general, the observations are done with an optical microscope and compared with computational models of growth. This work proposes a combination of crystallographic and cathodoluminescence data obtained in rocks from banded iron formations of the Iron Quadrangle in Brazil to represent an example of how complementary analytical techniques can be useful to understand geological problems. The chosen sample exhibits a strain fringe structure of quartz around a clast of magnetite partially transformed into goethite and hematite. Through the crystallographic data it was possible to identify the grain boundary morphology and domains of low deformation areas. On the other hand, the cathodoluminescence signal evidenced the occurrence of grains with a higher concentration of crystalline defects.

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We present the proof of concept of a general model that uses the tissue sample transmittance as input to estimate the depth-resolved attenuation coefficient of tissue samples using optical coherence tomography (OCT). This method allows us to obtain an image of tissue optical properties instead of intensity contrast, guiding diagnosis and tissues differentiation, extending its application from thick to thin samples. The performance of our method was simulated and tested with the assistance of a home built single-layered and multilayered phantoms (~100 µm each layer) with known attenuation coefficient on the range of 0.9 to 2.32 mm-1 . It is shown that the estimated depth-resolved attenuation coefficient recovers the reference values, measured by using an integrating sphere followed by the inverse adding doubling processing technique. That was corroborated for all situations when the correct transmittance value is used with an average difference of 7%. Finally, we applied the proposed method to estimate the depth-resolved attenuation coefficient for a thin biological sample, demonstrating the ability of our method on real OCT images.

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Many strategies have been developed for the synthesis of silicon carbide (SiC) thin films on silicon (Si) substrates by plasma-based deposition techniques, especially plasma enhanced chemical vapor deposition (PECVD) and magnetron sputtering, due to the importance of these materials for microelectronics and related fields. A drawback is the large lattice mismatch between SiC and Si. The insertion of an aluminum nitride (AlN) intermediate layer between them has been shown useful to overcome this problem. Herein, the high-power impulse magnetron sputtering (HiPIMS) technique was used to grow SiC thin films on AlN/Si substrates. Furthermore, SiC films were also grown on Si substrates. A comparison of the structural and chemical properties of SiC thin films grown on the two types of substrate allowed us to evaluate the influence of the AlN layer on such properties. The chemical composition and stoichiometry of the samples were investigated by Rutherford backscattering spectrometry (RBS) and Raman spectroscopy, while the crystallinity was characterized by grazing incidence X-ray diffraction (GIXRD). Our set of results evidenced the versatility of the HiPIMS technique to produce polycrystalline SiC thin films at near-room temperature by only varying the discharge power. In addition, this study opens up a feasible route for the deposition of crystalline SiC films with good structural quality using an AlN intermediate layer.

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Brazilian coffee is well known worldwide due to its quality and richness in taste. The aim of the present study is to provide the elemental characterization of Brazilian coffee along different stages of the drip brewing process. To that end, samples from roasted ground coffee, spent coffee, paper filters and the final beverage were analyzed with one single ion beam technique, namely particle-induced X-ray emission (PIXE). In total, over 140 samples from 8 different Brazilian brands of ground coffee were analyzed. Large differences in some elemental concentrations were observed among different brands and among different batches of a single brand, which leads to high variances in the data. Concerning the beverage preparation, the analysis of the spent coffee shows that the transfer ratio from the ground coffee to the beverage differs for each element. Our results indicate that potassium and chlorine have the highest transfer ratio. Moreover, the concentration of rubidium is relatively high in drinking coffee. Finally, there is no influence of the elemental composition of paper filter in the preparation of drinking coffee.

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Phantoms are important tools for image quality control and medical training. Many phantom materials have been proposed for ultrasound; most of them use water as the solvent, but these materials have disadvantages such as dehydration and low temporal stability if not properly stored. To overcome these difficulties, copolymer-in-oil gel was proposed as an inert and stable material; however, speed of sound for these materials is still lower than what is described for most biological tissues. Here, we propose the glycerol dispersion in oil-based gels to modify the acoustic and elastic properties of copolymer-in-oil phantoms. We manufactured copolymer-in-oil gels using styrene-ethylene/butylene-styrene (SEBS) in concentrations 8%-15%. We used 2 types of mineral oils with different viscosities. Glycerol was added in a volume fraction 0%-30% of the total amount of liquid. The acoustic (i.e., speed of sound, attenuation and backscattering) and the mechanical (i.e., density and Young's modulus) properties of the samples were within the range of values observed for soft tissues. The acoustic parameters of the samples were dependent on oil viscosity and glycerol concentration. The speed of sound ranged 1423 m/s - 1502 m/s, while the acoustic attenuation and the ultrasonic backscattering increased by adding glycerol. The density and the Young's moduli were less affected by the presence of glycerol. We conclude that glycerol can be used to control the acoustic parameters of copolymer-in-oil gels. Additionally, it opens the possibility of incorporating other oil-insoluble substances to control further properties of the phantom.

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The thermal instability of GeO2/Ge structures lasts as a barrier against the development of Ge-based metal-oxide-semiconductor devices. In the present work, stabilization was achieved through the incorporation of nitrogen into the oxide layer by thermally growing GeOxNy films in NO. With this approach, a stable layer is obtained in a single step as opposed to other nitridation techniques (like plasma immersion) which require additional processing. Significant reduction of GeO desorption from the surface and a strong barrier against additional substrate oxidation were obtained by the insertion of a small amount of nitrogen content (N/O ≈ 10%). Nuclear reaction analysis and profiling showed that nitrogen incorporation and removal occur simultaneously during film growth, yielding N to be distributed throughout the whole film, without accumulation in any particular region. Both the oxidation barrier and the lower GeO desorption rate are explained by a reduction of vacancy diffusivity inside the dielectric. This is not caused by the densification of the oxide, but is a consequence of nitrogen blockage of oxygen vacancy diffusion paths.

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RESUMEN Se analizan muestras de secciones transversales de esculturas en madera policromadas por los métodos de microanálisis: Microscopía óptica, las técnicas nucleares: microfluorescencia de rayos X y microemisión de rayos X inducida por protones con sistema de detección por dispersión de Rutherford acoplado y el método tradicional de Microscopía Electrónica de Barrido con detección de fluorescencia de rayos X dispersiva en energía acoplada. Se enfatiza en la microfluorescencia de rayos X por ser un método novedoso a partir del desarrollo alcanzado en la óptica de rayos X y que se puede implementar en un sistema convencional de FRX. Los resultados se comparan en cuanto a resolución espacial para diferenciar la estructura de capas pictóricas y sensibilidad elemental. Se determinaron el número de capas, su posición relativa, su espesor y la composición química de los pigmentos para caracterizar valiosas policromías de la otrora iglesia habanera San Juan de Letrán con el objetivo de obtener información acerca de la "historia materia"; que deba contribuir a su investigación de procedencia y atribución. Los pigmentos usados en esta obra artística se identificaron por los elementos característicos. Los mapas de distribución elemental obtenidos por las técnicas nucleares usadas, reproducen exactamente las estructuras observadas en las fotomicrografías obtenidas por medio de la microscopía de luz.

ABSTRACT Cross section samples from polychrome wood sculpture are analyzed by optical microscopy, the nuclear techniques: micro-X Ray Fluorescence, micro- Proton induced X-ray Emission coupled with Rutherford Backscattering and the traditional method by Scanning Electronic Microscopy with Energy Dispersive X-ray fluorescence detection (SEM-EDX) micro-analytical methods. Special emphasis is dedicated to µXRF, a novel advanced technique developed thanks to the last achievements of the X-ray optics that can be available by modifying conventional laboratory XRF spectrometer, representing an alternative to the traditional and expensive SEM-EDX stratigraphic analysis of pictorial works. The results are compared with respect to spatial resolution to differentiate pictorial layer structure and elemental sensitivity. Number of layer, relative position of layer, layer thickness and chemical composition of pigments are determined in the characterization of valuable polychromies of once church San Juan de Letrán in order to obtain information about their "material history" that should contribute to its provenance and attribution research. The pigments used in this artistic works were identified by their characteristic elements. The elemental distribution maps obtained by the used nuclear techniques precisely reproduced microphotographies obtained by means of Light Microscopy.