Viscoelastic properties of amorphous polymers 3: low molecular weight poly(methylphenylsiloxane)

By making creep and recoverable creep measurements of a nearly monodisperse low molecular weight poly(methyl phenyl siloxane) sample, we have found on decreasing temperature towardsT _g that there is continuously a change in the viscoelastic spectrum concomitant with a decrease of the steadystate recoverable compliance. This behavior is exactly the same as previously observed in low molecular weight poly(styrene), proving that this spectacular anomaly in the viscoelasticity of low molecular weight polymers is general and deserves an explanation. Photon correlation spectroscopic measurements performed on the same sample have extended the observation of the viscoelastic response to shorter times and the result corroborates the trend of variation established by the creep data.Dedicated to Prof.Dr. E. W. Fischer on his 65th Birthday. Prof.Dr. Fischer is known for his valuable contribution to fosterine, international collaboration of research in polymer science. This work is an example of his contribution because it would not be possible without him bringing us together. One of us (KLN) would like to take this opportunity to thank Prof. Dr. Fischer for his unwaiving support of the 1st (Crete) and the 2nd (Alicante) International Discussion Meeting on Relaxations in Complex Systems     

Influence of Cyclodextrins on the Kinetics of Oxidation of Amino Acids and BSA by Hydrazyl Radicals

The kinetics of oxidation of amino acids (Arg, His, Lys, Phe, Thr and Tyr), a dipeptide (Gly-His), and BSA (bovine serum albumin) by two persistent water soluble free radicals of the hydrazyl type has been studied.The rate decreases in the order Arg>Lys>Tyr>Thr>HisBSAPheGly-His with bothfree radicals. Addition to the reaction mixture of - and -cyclodextrin decreases the oxidation rate, probably due to amino acidencapsulation in the cyclodextrin cavity. -Cyclodextrin protects more efficiently against oxidation than -cyclodextrin.     

The microscopic investigation of structures of moving flux lines by neutron and muon techniques

We have used a variety of microscopic techniques to reveal the structure and motion of flux line arrangements, when the flux lines in low T _c type II superconductors are caused to move by a transport current. Using small-angle neutron scattering by the flux line lattice (FLL), we are able to demonstrate directly the alignment by motion of the nearest-neighbor FLL direction. This tends to be parallel to the direction of flux line motion, as had been suspected from two-dimensional simulations. We also see the destruction of the ordered FLL by plastic flow and the bending of flux lines. Another technique that our collaboration has employed is the direct measurement of flux line motion, using the ultra-high-resolution spectroscopy of the neutron spin-echo technique to observe the energy change of neutrons diffracted by moving flux lines. The muon spin rotation (μSR) technique gives the distribution of values of magnetic field within the FLL. We have recently succeeded in performing μSR measurements while the FLL is moving. Such measurements give complementary information about the local speed and orientation of the FLL motion. We conclude by discussing the possible application of this technique to thin film superconductors.     

Radiochromic gel dosemeter for three-dimensional dosimetry

A gel dosemeter in which ionising radiation causes a colour change was produced by modifying an existing Fricke gel system. This allows a more convenient preparation procedure and gives a better quality dosimetric system for three-dimensional (3-D) dose measurements. The role of three active components of the Ferrous sulphate Xylenol orange Gelatin (FXG) gel dosemeter is quantified with special consideration of their effect on system sensitivity and stability. The optimal composition was found to be 0.5 mM ferrous sulphate, 0.1 mM xylenol orange and 25 mM sulphuric acid. The dose response is linear in the range 0.1–30 Gy. The FXG sensitivity, derived from the gradient of the dose response curve, was found to be ΔA=0.084 cm⁻¹ Gy⁻¹, where A is the optical absorption coefficient at a wavelength of 585 nm, with reproducibility and 24 h stability of better than 5%.     

Spectral modulation detection as a function of modulation frequency, carrier bandwidth, and carrier frequency region

The present study investigates the nature of spectral envelope perception using a spectral modulation detection task in which sinusoidal spectral modulation is superimposed upon a noise carrier. The principal goal of this study is to characterize spectral envelope perception in terms of the influence of modulation frequency (cycles/octave), carrier bandwidth (octaves), and carrier frequency region (defined by lower and upper cutoff frequencies in Hz). Spectral modulation detection thresholds measured as a function of spectral modulation frequency result in a spectral modulation transfer function (SMTF). The general form of the SMTF is bandpass in nature, with a minimum modulation detection threshold in the region between 2 to 4 cycles/octave. SMTFs are not strongly dependent on carrier bandwidth (ranging from 1 to 6 octaves) or carrier frequency region (ranging from 200 to 12 800 Hz), with the exception of carrier bands restricted to very low audio frequencies (e.g., 200-400 Hz). Spectral modulation detection thresholds do not depend on the presence of random level variations or random modulation phase across intervals. The SMTFs reported here and associated excitation pattern computations are considered in terms of a linear systems approach to spectral envelope perception and potential underlying mechanisms for the perception of spectral features.     

Investigation of the quantitative properties of the quadrupole orthogonal acceleration time-of-flight mass spectrometer with electrospray ionisation using 3,4-methylenedioxymethamphetamine

This paper describes the investigation of the potential of a quadrupole orthogonal acceleration time-of-flight mass spectrometer (Q-TOF) equipped with an atmospheric pressure ionisation interface for quantitative measurements of small molecules separated by reversed phase liquid chromatography. To this end, the detection limits and linear dynamic range in particular were studied in an LC/MS/MS experiment using 3,4-methylenedioxymethamphetamine standards and 3,4-methylenedioxyethylamphetamine for internal standardisation. In a second phase, the experiment was repeated with real biological extracts (whole blood, serum, and vitreous humour). A calibration for 3,4-methylenedioxymethamphetamine and its metabolite 3,4-methylenedioxyamphetamine was prepared in each of these matrices again using 3,4-methylenedioxyethylamphetamine as internal standard. The resulting quantitative data were compared with those obtained by liquid chromatography with fluorescence detection for the same extracts. The Q-TOF results revealed excellent sensitivity and a linear dynamic range of nearly four decades (2-10 000 pg on-column, r(2) = 0.9998, 1/x weighting). Furthermore, all the calibration curves prepared in biological material were superimposable, LC/MS/MS and LC-fluorescence, and the quantitative results for actual samples compared very favourably. It was concluded that the Q-TOF achieves a linear dynamic range for quantitative LC/MS/MS work exceeding that of fluorescence detection and at much better absolute sensitivity. Copyright 1999 John Wiley & Sons, Ltd.     

Radiometric characterization of radiochromic gel material applied for UVA radiation dosimetry

Diverse kinds of chemical products are useful for UVA dosimetry due to chemical incitation properties of ultraviolet radiation. It was recognized and approved that radiochromic gel materials have a specific behavior under UVA radiation exposure. The relationship between the UVA dose and the variation of visible light absorbance was found to follow a second-order function with good accuracy. Specific metrological properties of the gel material for radiometric UVA dosimetry application were studied at irradiation levels simulate deferent natural solar UVA radiation levels. The behavior of the gel absorbance properties, detector linearity, induced reaction and temporal and radiometric stability at various dose rate levels were investigated. The relationship between UVA dose and changes in optical absorbance is found independent of the UVA exposure rate including the solar UVA maximum level which could be detected at sea level. The studied gel material absorbs more than 90% of UVA radiation in 1 cm of the gel thickness. Gel detector linearity was investigated over a UVA range (20-84 W/m²) which exceeds the natural solar UVA radiation level and the linearity factor was found to be close to 1 with statistical differences ≤ 2%. The UVA induced dark reaction in the gel material continues for almost 4 min after stopping irradiation; which must be considered during measurements. The detector has good temporal stability even under high UVA exposure; hence the gel absorption in the UVA spectrum region is stable. Measured deviation was less than 1%, and relative variation of gel optical absorbance in UVA spectrum is about 35 times lower than that occur in visible region.