Magnetic Properties of Fe/Ni and Fe/Co Multilayer Thin Films

In this work, the magnetic and transport properties of Fe/SiO₂/Ni and Fe/SiO₂/Co multilayers grown on Si/SiO₂ substrates have been studied. The samples have been prepared by two-stage deposition process. In the first stage, Fe layer and SiO₂ interlayer of both samples are grown by ion beam deposition technique at room temperature. Then the samples are taken out to ambient atmosphere and loaded into a pulse laser deposition (PLD) chamber. Prior to the deposition of top layer, the samples are cleaned by annealing at 150 °C. In the second stage, Ni (or Co) layer is prepared by PLD technique at room temperature. The thickness of deposited layers has been measured by Rutherford back scattering (RBS). Magnetic properties of ferromagnetic bilayers have been investigated by room-temperature ferromagnetic resonance (FMR) and vibrating sample magnetometer (VSM) techniques. Standard four-point magneto-transport measurements at various temperatures have been performed. Two-step switching in the in-plane hysteresis loops of Fe/SiO₂/Ni and Fe/SiO₂/Co samples is observed. A crossing in the middle of hysteresis loops of both samples points to a weak antiferromagnetic interaction between the magnetic layers of the stacks. Saturation magnetization values have been obtained from the VSM measurements of samples with DC magnetic field perpendicular to the films surface. Magneto-transport measurements have shown the predominant contribution of anisotropic magnetic resistance both at room and low temperatures. FMR studies of Fe/SiO₂/Ni and Fe/SiO₂/Co samples have revealed additional non-uniform (surface and bulk SWR) modes, which behavior has been explained in the framework of the surface inhomogeneity model. An origin of the antiferromagnetic interaction has been discussed.     

Quantification of benzene,toluene, ethylbenzene and o-xylene in internal combustion engine exhaust with time-weighted average solid phase microextraction and gas chromatography mass spectrometry

A new and simple method for benzene, toluene, ethylbenzene and o-xylene (BTEX) quantification in vehicle exhaust was developed based on diffusion-controlled extraction onto a retracted solid-phase microextraction (SPME) fiber coating. The rationale was to develop a method based on existing and proven SPME technology that is feasible for field adaptation in developing countries. Passive sampling with SPME fiber retracted into the needle extracted nearly two orders of magnitude less mass (n) compared with exposed fiber (outside of needle) and sampling was in a time weighted-averaging (TWA) mode. Both the sampling time (t) and fiber retraction depth (Z) were adjusted to quantify a wider range of C_gas. Extraction and quantification is conducted in a non-equilibrium mode. Effects of C_gas, t, Z and T were tested. In addition, contribution of n extracted by metallic surfaces of needle assembly without SPME coating was studied. Effects of sample storage time on n loss was studied. Retracted TWA–SPME extractions followed the theoretical model. Extracted n of BTEX was proportional to C_gas, t, D_g, T and inversely proportional to Z. Method detection limits were 1.8, 2.7, 2.1 and 5.2 mg m⁻³ (0.51, 0.83, 0.66 and 1.62 ppm) for BTEX, respectively. The contribution of extraction onto metallic surfaces was reproducible and influenced by C_gas and t and less so by T and by the Z. The new method was applied to measure BTEX in the exhaust gas of a Ford Crown Victoria 1995 and compared with a whole gas and direct injection method.     

Polycondensation of low-active monomers in mesomorphic-like reaction mixtures and in presence of polymeric matrix

The study results of the synthesis of polyheterocycles based on dianhydrides, obtained by photochemical reaction of aromatic compounds with maleic anhydride, have been presented. In comparison with aromatic analogues the low reactivity of anhydride cycles is characteristic for tricyclodecenetetracarboxylic dianhydrides. This fact made unsuitable the traditional two-stage method to synthesize high-molecular polyheterocycles on the basis of these monomers. There has been estimated a possibility of chain growth of oligomeric polyamic acids (PAMA) in mesomorphic-like state of its solutions in mixed solvents. In this conditions the PAMA polymerization degree changed from 7 up to 60. These peculiarities have given the opportunity to synthesize polyheterocycles in mild conditions. The features of polycondensation of tricyclodecenetetracarboxylic dianhydrides with bis(4-aminophenyl) ether in the presence of poly-4-vinylpyridine, polyacrylic and polymethacrylic acids have been studied. There have been synthesized high-molecular-weight polyimides and polyamidoimides, possessing good physicomechanical and thermal properties.     

Asymmetric Ring Opening in a Tetrazine-Based Ligand Affords a Tetranuclear Opto-Magnetic Ytterbium Complex

We report the formation of a tetranuclear lanthanide cluster, [Yb₄(bpzch)₂(fod)₁₀] ( 1 ), which occurs from a serendipitous ring opening of the functionalised tetrazine bridging ligand, bpztz (3,6-dipyrazin-2-yl-1,2,4,5-tetrazine) upon reacting with Yb(fod)₃ (fod⁻=6,6,7,7,8,8,8-heptafluoro-2,2-dimethyl-3,5-octandionate). Compound 1 was structurally elucidated via single-crystal X-ray crystallography and subsequently magnetically and spectroscopically characterised to analyse its magnetisation dynamics and its luminescence behaviour. Computational studies validate the observed M_J energy levels attained by spectroscopy and provides a clearer picture of the slow relaxation of the magnetisation dynamics and relaxation pathways. These studies demonstrate that 1 acts as a single-molecule magnet (SMM) under an applied magnetic field in which the relaxation occurs via a combination of Raman, direct, and quantum tunnelling processes, a behaviour further rationalised analysing the luminescent properties. This marks the first lanthanide-containing molecule that forms by means of an asymmetric tetrazine decomposition.     

Polyurethanes as Carriers of Antitumorous Drugs

Drug delivery systems on a polyurethane base with various antitumorous drugs, such as cyclophosphane, thiophosphamide and vincristine, have been prepared. An in vitro technique was used to determine the release characteristics of the drugs into model biological media. It was shown the drug release occurs in accordance with first-order kinetics, as well a maximum degree for the drug loading were studied. The thermodynamic parameters of drug release has been determined. It was illustrated that the activation energies were 4.3, 3.9 and 3.2 kcal/mole for cyclophosphane, thiophosphamide and vincristine respectively, corresponding to a diffuse-controlled mechanism of release. © 1998 John Wiley & Sons, Ltd.     

Investigation of the Hydrogen Etching Effect of the SiC Surface on the Formation of Graphene Films

Technical Physics - We have studied the effect of temperature and etching duration of the 4H-SiC (0001) surface in hydrogen on the structural perfection of graphene films grown by thermal...     

Temperature fields control in the process of spark plasma sintering of thermoelectrics

The process of creating thermoelectrics by spark plasma sintering of nanostructured powders in order to obtain materials with improved thermoelectric properties has been modeled. The factors that influence the distribution of thermal field in the sintering process have been analyzed. The influence of geometric parameters of tooling on the formation of temperature gradient field required for effective sintering of functionally gradient materials and segmented branches of thermo-elements has been considered. The results can be used to determine the conditions and modes of sintering of functionally gradient materials in installations of spark plasma sintering and hot pressing.     

Quantification of Transformation Products of Unsymmetrical Dimethylhydrazine in Water Using SPME and GC-MS

Quantification of trace concentrations of transformation products of rocket fuel unsymmetrical dimethylhydrazine (UDMH) in water requires complex analytical instrumentation and tedious sample preparation. The goal of this research was to develop a simple and automated method for sensitive quantification of UDMH transformation products in water using headspace (HS) solid-phase microextraction (SPME) in combination with GC-MS and GC-MS/MS. HS SPME is based on extraction of analytes from a gas phase above samples by a micro polymer coating followed by a thermal desorption of analytes in a GC inlet. Extraction by 85 µm Carboxen/polydimethylsiloxane fiber at 50 °C during 60 min provides the best combination of sensitivity and precision. Tandem mass spectrometric detection with positive chemical ionization improves method accuracy and selectivity. Detection limits of twelve analytes by GC-MS/MS with chemical ionization are about 10 ng L^?1. GC-MS provides similar detection limits for five studied analytes; however, the list of analytes detected by this method can be further expanded. Accuracies determined by GC-MS were in the range of 75–125% for six analytes. Compared to other available methods based on non-SPME sample preparation approaches (e.g., liquid–liquid and solid-phase extraction), the developed method is simpler, automated and provides lower detection limits. It covers more UDMH transformation products than available SPME-based methods. The list of analytes could be further expanded if new standards become available. The developed method is recommended for assessing water quality in the territories affected by space activities and other related studies.