SIMS investigations of ion beam induced PVK fragmentation

Summary The mass spectra of secondary ions emitted from PVK thin layers under 2 keV Xe⁺ bombardment were measured. The charasteristic elemental and molecular ions emitted were specified. The temperature dependence of the secondary emission was also measured. The results obtained were briefly discussed in terms of the ion beam-induced polymer structure fragmentation.Work supported by the research programme MR-I-5-8.     

Quantitative microstructural characterisation of Fe–30Ni alloy after martensitic transformations by means of stereological and magnetic methods

In the Fe–30Ni alloy investigated a martensitic transformation can occur both during quenching or plastic deformation. Martensite formed during plastic deformation, depending on the thermo-mechanical treatment applied, exhibits a different morphology from that achieved during quenching and forms the so-called composite-like structure. The morphology and volume fraction of martensite depends both on strain and temperature. In the present studies Fe–30Ni alloy was deformed by monotonic rolling in one path and perpendicular rolling in the temperature range M_D–M_S. The aim of the investigations was a determination of martensite volume fraction depending on the strain and temperature. To examine the influence of strain, the alloy was deformed by rolling in one path or perpendicular rolling at a temperature of − 30 °C, in the strain range of 10–30%. The dependence of temperature was investigated by rolling with 30% strain in a temperature range from − 30 °C to − 80 °C. The variants of thermo-mechanical treatment performed enabled us to achieve different martensite morphologies and volume fractions. Microstructural analysis was performed by means of light microscopy and transmission electron microscopy. The results of quantitative microstructural analysis of martensite and retained austenite volume fractions formed in different thermo-mechanical treatments were compared with those obtained by magnetic measurements. The fraction of deformation-induced martensite determined varied from 2% to 86%. The partial volume fractions V_V^MF of martensite formed in different deformation directions were also determined. It was found that the influence of the temperature on the martensite volume fraction is more pronounced than the influence of strain.     

Two-dimensional deghosting for EPI

A residual ghost artefact in echo-planar imaging (EPI) remains after the standard correction procedure based on a 1-dimensional phase-modulation of the spectra of even or odd echoes. A better reduction of this artefact is demonstrated using a 2-dimensional phase correction. The phase correction map is measured inside the ghost-free region of the image, preferably in a reference scan with an increased field of view, as the phase difference between complex images reconstructed separately from even and odd echoes. An extrapolated map consisting of spatial components up to the second order (constant,x, y, xy andx ²−y²) is then found by a fit to the measured values. This map is used to correct the phase of even- and odd-reconstructed images before adding them. This procedure may cause some spatially dependent loss of signal, but if the level of the residual artefact is less than 20% of the image intensity, such losses are negligible.     

The Structural Elucidation of Oligomeric Blue Dyes Derived from 9-Alkylcarbazoles

Carbazoles react with a variety of one-carbon fragments at the 3- or 3,6-positions to give di- and trimeric products with CH₂: links. These precursors react by losing hydride ion to give blue oligomeric dyes. Carbazoles substituted in the 9-position by CH₂SPh, CH₂SOPh, and CH₂SO₂Ph rearrange to give carbazole oligomers linked at the 3,6-positions. Products are characterised spectrally, and their mechanism of formation is discussed.     

Changes in the contents of mono-, di- and oligosaccharides in leek plants stored in cold room

The aim of this work is to present the results of the analysis of composition of mono-, di- and oligosaccharides, including the content of fructooligosaccharides as well as rafinose, stachyose in pseudo stalk of leek plants of the following cultivars: Shelton F1, Belton F1 and Parton F1. Leek plants were stored in cold room at the temperature 0 °C and relative humidity around 98% in the period from December to May. Fructose, glucose, saccharose, fructooligosaccharides (FOS) as well as α-galactosides were determined with the HPLC method with the application of water-alcohol extracts. It was shown that some of the studied parameters have changed during storage, i.e., the glucose content increased from 4.4 ± 0.3 to 16.2 ± 1.6, fructose from 4.7 ± 0.2 to 23.8 ± 0.4, saccharose from 5.1 ± 0.7 to 18.7 ± 0.1, depending on the cultivar and the storage period. The largest increase in the content of fructose and glucose took place between 60th and 90th day of storage which testifies to intensive hydrolysis of fructans. Leek cv. Parton F1 was characterised by the largest content of fructans and the lowest susceptibility to hydrolysis. The amount of kestose, nystose and rafinose after the period of storage changed from 0.3 ± 0.0 to 0.9 ± 0.2, 0.5 ± 0.1 to 1.8 ± 0.1, 0.8 ± 0.1 to 1.8 ± 0.2 g/100 g of dry mass, respectively. The content of stachyose, in turn, remained at a constant level and amounts to around 0.5 g/100 g of dry mass. Leek plants kept in typical refrigeration conditions are characterised by good durability and constitute a valuable merchandise. However, due to ongoing hydrolysis processes, the content of prebiotic substances decreased what lowered the health-promoting value.     

Fields of strains around the inclusion of second phase in a uniform matrix undergoing plastic deformation

This paper focuses on the problem of the evaluation of strains around the inclusions of various shapes and properties located in the uniform matrix undergoing large plastic deformations. The analysis is performed using the rigid-plastic finite-element approach. The uniform plane-strain deformation field is simulated by an introduction of zero friction forces into the program for the compression process. An assumption that the die is wider than the sample allows to simulate ideally uniform flow of metal. Several shapes of the inclusions are investigated, but the results for three most common shapes of the particle's cross-section are presented in the paper. They are: square with the sides parallel to the main directions, square with the sides inclined under an angle of 45° to the main directions and round.     

Preliminary results on a new polymer electrolyte,poly(ethyleneoxide)-Hg(CIO4)2

A new solid polymer electrolyte, poly(ethylene oxide)-Hg(ClO₄)₂, has been prepared with the ratio of ethylene oxide units to mercury ions ranging from 4 to 20. The variation of conductivity with temperature does not follow a simple Arrhenius law. At high salt concentrations the films are entirely amorphous.     

Potential of the Pb,PbSO4/H2SO4 electrode at temperatures up to 240°C

Standard lead—lead sulphate electrode potential was determined over the temperature range 20–240°C from emf measurements of the Pb, PbSO₄H₂SO₄ (0.05M)K₂SO₄KClHCl(0.1M)/AgCl, Ag and Pb, PbSO₄H₂SO₄(m)K₂SO₄H₂SO₄(0.05M)PbSO₄, Pb cells where m = 0.005, 0.01, 0.1 and 0.5 M. To this effect lead—lead sulphate electrode potential was calculated using the temperature relationship of the standard silver—silver chloride electrode potential and activity coefficients of hydrochloric acid determined by Greeley et al. at temperatures up to 260°C. Diffusion potentials occurring at the phase boundaries in the cells under investigation were calculated using the Henderson's equation. Values of the standard lead—lead sulphate electrode potential were determined by extrapolation of the E°′ function to the zero ionic strength which was calculated using the second sulphuric acid dissociation constant determined by Lietzke et al. at temperatures up to 300°C. The standard electrode potential was described in the temperature range 20–240°C by the following relationship: E°_{Pb, PbSO4/SO^2?4}(V) = 0.040-0.00126T. A change in entropy ΔS° of the electrode reaction Pb + SO^2?₄ = PbSO₄ + 2e^? is constant in this temperature range and is ?243 JK^?1 mol^?1 (?1018 cal K^?1 mol^?1).     

Biological Availability and Preliminary Selenium Speciation in Selenium-Enriched Mycelium of Lentinula edodes (Berk.)

Our goal is to obtain a new food supplement — a chemopreventive preparation derived from selenium (Se)-enriched Lentinula edodes mycelium. In the present study the bioavailability of selenium from Se-enriched mycelium preparations was tested in vitro and in vivo. Three different preparations of selenated mycelium were compared: dried mycelium, lyophilized mycelium, and lyophilized-autolyzed mycelium. In vitro, estimated Se bioavailabilities were 60%, 82%, and 98%, respectively. In vivo bioavailability was determined in rats. As reference, sodium selenite and Se yeast formulations were used at an Se-equivalent dose. The pharmacokinetic data for tested mycelial preparations suggest a rapid but incomplete Se absorption, and rapid elimination, without risk of accumulation. The speciation of selenium in Se-enriched mycelial cultures was carried out by specific oxido-reduction reactions. For tested mycelium the main part of Se was in the 0 and IV oxidation states in inorganic form or combined in a lipid or carbohydrate structure, about 47% was in the –II state in Se-amino acids or in other undefined water- or alcohol soluble organic compounds. Differences in pharmacokinetic data for Se yeast and L. edodes mycelial formulations probably arise from differences in Se speciation. Our data suggest that formulations of selenized Lentinula edodes mycelium could be used in chemoprevention as food supplements.