Determination of the Composition of the Surface Layer of Binary Metal Alloys

We have analyzed the effect of various parameters (surface tensions of the components, molar volumes of the components and the solution, compression and depression in alloy formation, activity coefficients of the components in the melt) on the shape of the surface tension isotherm as a function of the surface layer composition. We compare the analysis results with experimental data. We propose a method for estimating the composition of the surface layer based on a model assuming an additive variation in the surface tension of the solution as a function of the composition of the surface layer. We have calculated the concentration of the surface-active component in the surface layer of melts in the systems Ge - Sn, Ge - Pb, and Ge - Bi.__________Translated from Poroshkovaya Metallurgiya, Nos. 1–2(441), pp. 60–67, January–February, 2005.     

Microwave remote sensing of physically buried objects in the Negev Desert: implications for environmental research

We report remote detections of physically buried specularly reflecting objects using microwave radar at two sites: Ashalim and Tseelim in the northern region of the Negev Desert, Israel. These detections provide confirmation that microwave subsurface remote sensing is a genuine phenomenon. At Ashalim, a scatterometer operating in the P-band (441 MHz, 68 cm) was mounted on a cherry picker truck at a height of 8 m and used to detect two triangular aluminum mesh reflectors (forming a 1-m square area reflector) buried down to a depth of 8 cm in dry sand. At Tseelim, the same scatterometer was mounted on an airplane flying at an altitude of 70 m and used to detect 1-m square aluminum reflectors (each one submerged at a different location along the airplane flight path) buried down to a depth of 20 cm. The experimental results compare favorably with a theoretical model that incorporates radar absorption effects arising in the sandy subsurface layer and radar interference effects arising from phase differences between reflections from the surface and buried reflector. The theoretical modeling also predicts the detection of a subsurface reflector down to a depth of about 4.4 m. This experiment and the associated modeling approach is the first of a series of planned experiments, which we outline for the detection and the theoretical evaluation of buried reflectors using remote microwave and VHF radar. We identify potential subject areas for environmental research.     

Compaction Kinetics with Liquid-Phase Sintering of W – Ni – Sn Pseudoalloys

A kinetic equation for compaction with liquid-phase sintering is found on the basis of rheological sintering theory. Kinetic coefficients of the equation are determined from physicochemical properties of a dispersed system and its components. Compaction kinetics are studied for the system W – Ni – Sn where the liquid phase is eutectic alloy Ni – Sn with the greatest nickel content. It is shown that experimental results are in good agreement with those obtained by the kinetic equation on the coordinates porosity – time. Diffusion coefficient is evaluated for tungsten in melt (67.5 mass% Ni + 32.5 mass% Sn): at 1200°C it is 0.113·10_–5 cm₂/sec for grain diameter L ₀ = 3 μm. Time dependences are also obtained for the compaction rate and viscosity of the pseudoalloys studied.     

Facile Microwave Assisted Synthesis of Silver Nanostars for Ultrasensitive Detection of Biological Analytes by SERS

We report a very simple, rapid and reproducible method for the fabrication of anisotropic silver nanostars (AgNS) that can be successfully used as highly efficient SERS substrates for different bioanalytes, even in the case of a near-infra-red (NIR) excitation laser. The nanostars have been synthesized using the chemical reduction of Ag⁺ ions by trisodium citrate. This is the first research reporting the synthesis of AgNS using only trisodium citrate as a reducing and stabilizing agent. The key elements of this original synthesis procedure are rapid hydrothermal synthesis of silver nanostars followed by a cooling down procedure by immersion in a water bath. The synthesis was performed in a sealed bottom flask homogenously heated and brought to a boil in a microwave oven. After 60 s, the colloidal solution was cooled down to room temperature by immersion in a water bath at 35 °C. The as-synthesized AgNS were washed by centrifugation and used for SERS analysis of test molecules (methylene blue) as well as biological analytes: pharmaceutical compounds with various Raman cross sections (doxorubicin, atenolol & metoprolol), cell lysates and amino acids (methionine & cysteine). UV-Vis absorption spectroscopy, (Scanning) Transmission Electron Microscopy ((S)TEM) and Atomic Force Microscopy (AFM) have been employed for investigating nanostars’ physical properties.     

Oregano: chemical analysis and evaluation of its antimalarial, antioxidant, and cytotoxic activities

Abstract: GC‐FID and GC‐MS analysis of essential oil from oregano leaves (Origanum compactum) resulted in the identification of 46 compounds, representing more than 98% of the total composition. Carvacrol was the predominant compound (36.46%), followed by thymol (29.74%) and p‐cymene (24.31%). Serial extractions with petroleum ether, ethyl acetate, ethanol, and water were performed on aerials parts of Origanum compactum. In these extracts, different chemical families were characterized: polyphenols (gallic acid equivalent 21.2 to 858.3 g/kg), tannins (catechin equivalent 12.4 to 510.3 g/kg), anthocyanins (cyanidin equivalent 0.38 to 5.63 mg/kg), and flavonoids (quercetin equivalent 14.5 to 54.7 g/kg). The samples (essential oil and extracts) were subjected to a screening for antioxidant (DPPH and ABTS assays) and antimalarial activities and against human breast cancer cells. The essential oil showed a higher antioxidant activity with an IC₅₀= 2 ± 0.1 mg/L. Among the extracts, the aqueous extract had the highest antioxidant activity with an IC₅₀= 4.8 ± 0.2 mg/L (DPPH assay). Concerning antimalarial activity, Origanum compactum essential oil and ethyl acetate extract showed the best results with an IC₅₀ of 34 and 33 mg/mL, respectively. In addition, ethyl acetate extract (30 mg/L) and ethanol extract (56 mg/L) showed activity against human breast cancer cells (MCF7). The oregano essential oil was considered to be nontoxic.     

Fate of ivermectin residues in ewes' milk and derived products

The fate of ivermectin (IVM) residues was studied throughout the processing of daily bulk milk from 30 ewes (taken up to 33 d following subcutaneous administration of 0.2 mg IVM/kg b.w.) in the following milk products: yoghurt made from raw and pasteurized milk; cheese after pressing; 30- and 60-day ripened cheese; and whey, secondary whey and whey proteins obtained after cheese-making (albumin cheese). The concentration of the H2B1a component of IVM was analysed in these dairy products using an HPLC method with fluorescence detection. The mean recovery of the method was, depending on the matrix, between 87 and 100%. Limits of detection in the order of only 0.1 microg H2B1a/kg of product were achieved. Maximum concentrations of IVM were detected mostly at 2 d after drug administration to the ewes. The highest concentration of IVM was found on day 2 in 60-day ripened cheese (96 microg H2B1a/kg cheese). Secondary whey was the matrix with the lowest concentration of IVM (<0.6 microg H2B1a/ kg). Residue levels fell below the limits of detection between day 5 (for secondary whey) and day 25 (for all cheese samples). In the matrices investigated, linear correlations between daily concentrations of IVM, milk fat and solid content were evident. During yoghurt production, fermentation and thermal stability of IVM was observed. During cheese production, approximately 35% of the IVM, present in the raw (bulk) milk samples, was lost. From the results it was concluded that the processing of ewes' milk did not eliminate the drug residues under investigation. The consequences of IVM in the human diet were discussed. Milk from treated animals should be excluded from production of fat products like cheese for longer after treatment with IVM than for lower fat products.     

The influence of iodide on glass transition temperature of high-pressure nuclear waste glasses

The glass transition temperature (T_g) is a key parameter to investigate for application in nuclear waste immobilization in borosilicate glasses. T_g for several glasses containing iodine (I) has been measured in order to determine the I effect on T_g. Two series of glass composition (ISG and NH) containing up to 2.5 mol% I and synthesized under high pressure (0.5 to 1.5 GPa) have been investigated using differential scanning calorimetry (DSC). The I local environment in glasses has been determined using X-ray photoelectron spectroscopy and revealed that I is dissolved under its iodide form (I⁻). Results show that T_g is decreased with the I addition in the glass in agreement with previous results. We also observed that this T_g decrease is a strong function of glass composition. For NH, 2.5 mol% I induces a decrease of 24°C in T_g, whereas for ISG, 1.2 mol% decreases the T_g by 64°C. We interpret this difference as the result of the I dissolution mechanism and its effect on the polymerization of the boron network. The I dissolution in ISG is accompanied by a depolymerization of the boron network, whereas it is the opposite in NH. Although ISG corresponds to a standardized glass, for the particular case of I immobilization it appears less adequate than NH considering that the decrease in T_g for NH is small in comparison to ISG.