Fast nonequilibrium induction detectors based on thin superconducting films

A new type of fast detector is proposed. The operation of the detector is based on the change induced in the kinetic inductance of NbN and YBa₂Cu₃O_7−δ superconducting films by nonequilibrium quasiparticles produced by electromagnetic radiation. The speed of a NbN detector is essentially temperature-independent and is less than 1 ps. A model based on the Omen-Scalapino scheme describes well the experimental dependence of the voltage-power sensitivity of a NbN detector on the modulation frequency of the radiation. A low equilibrium quasiparticle density and a high quantum yield give detecting power D*=10¹²W⁻¹ · cm · Hz^1/2 at temperature T=4.2 K and D*=10¹⁶ W⁻¹ · cm · Hz^1/2 at temperature T=1.6 K. The time constant of the low-temperature YBaCuO induction detector is determined only by the electron-phonon interaction time τ _e-ph ^d in the nodal regions. Zh. Tekh. Fiz. 68, 63–69 (October 1998)     

Effect of thermomechanical processing on microstructural evolution and deformation behaviour of polycrystalline magnesium under quasi-static and high strain rate conditions

Abstract

The effect of thermomechanical processing on microstructure evolution and room temperature flow behaviour of polycrystalline magnesium in compression at strain rates of ~10^?2 and ~10³ s^?1 was investigated. Different initial microstructures were produced by optimising rolling and annealing cycles. Prior to annealing for 1 h at 350 °C, Mg samples were processed by two different treatments such as (i) hot rolling at 350 °C and (ii) hot rolling at 350 °C plus cold rolling at room temperature. Introduction of cold working step led to an increased fraction of hard oriented grains with a marginal grain size difference in post-annealed samples. A profound effect of thermomechanical processing on strain hardening rate as well as rate-sensitive flow behaviour of Mg was observed. The influence of prior processing history and strain rate on flow behaviour of Mg was clearly reflected in terms of texture strengthening/weakening phenomena and formation of microstructural deformation bands.     

A CCD based detector for quick detection of pressure induced phase transitions

Abstract

A high sensitivity CCD based two dimensional angle dispersive X-ray are a detector has been developed for quick detection of pressure induced phase transitions for a laboratory X-ray source such as a rotating anode generator. The performance of this detector was tested by successfully carrying out powder X-ray diffraction measurements on element Pd, intermetallics AuIn², AuGa² and low Z scatterer adamantane (C₁₀H_l6) at ambient conditions. Its utility for quick detection of phase transitions at high pressures with diamond anvil cell (DAC) is demonstrated by reproducing the known pressure induced structural phase transitions in RbI and KI. The importance of this detector system in search of unknown phase transitions has been established by observing new structural phase transitions in In_0.25Sn_0.75 and AuGa₂. Various softwares have also been developed such as interactive location of centre of diffraction rings, radial integration and image enhancement to analyze data from this detector.     

STUDY OF HEAVY ION MODIFIED CR-39 (DIETHYLENEGLYCOL BISALLYL CARBONATE)

The commercially available solid state nuclear track detector CR-39 was bombarded with 100 MeV Si⁸⁺ ions. The Fourier transfonned infrared (FTIR) spectroscopic technique was employed for studying the changes in chemical properties whereas differential scanning calorimetry was used for studying the changes in thermal properties. It was observed that there were substantial chemical modifications in the sample, such as the breaking of C-0 single bonds and the formation of phenolic 0-H bonds. lt was further observed that CR-39 is amorphous and rigid and shows no glass transition temperature.     

Non-empirical calculation of the electronic energy levels of the BF3 + ion. Interpretation of the photoelectron spectrum of BF3

There is a strong interaction between Na⁺ ions and the stable nitroxide radical 2,2,6,6-tetramethyl piperidinyl oxide (TMPN) in THF solution. The paramagnetic shift of the ²³Na resonance indicates that positive unpaired spin density is present at the sodium nucleus. The temperature dependence of the contact shift shows that complex formation is entropy-driven, since the TMPN - Na⁺ complex is endothermic by 8 ± 0·4 kJ mol^-1. Ab initio calculations, performed on a model system, indicate that attachment of the sodium cation to oxygen or to nitrogen leads to conformations whose energies are rather similar; only II(N) geometries are characterized by positive spin densities on sodium, as found experimentally. The longitudinal and transverse relaxation rates also point, from their relative magnitudes, to a predominant contribution from scalar I · S coupling, confirming a considerable degree of spin density transfer from the radical to the sodium nucleus.     

Enthalpy Relaxation Study of Poly(Vinyl Chloride) Films Based on the Time-Temperature Superposition Principle

Abstract

In the enthalpy relaxation of poly(vinyl chloride), a decrease in enthalpy upon the isothermal ageing was measured using the differential scanning calorimetry method as a function of ageing time (t_A) and ageing temperature. The range of the ageing temperature was from 56?°C (T_g ? 25?°C) to 72?°C (T_g ? 9?°C) where T_g denotes the glass transition temperature. The limiting value of the decrease in enthalpy was determined by applying a stretched exponential function to the measured enthalpy data. The relaxation function (?) was derived from the measured enthalpy and the construction of a master curve was tried by shifting the ? ? t_A curves of the respective ageing temperatures horizontally. Although there was no agreement between the shift factors (a_T) and the relaxation times of the ? ? t_A curves, the superposition was successfully constructed and the a_T values obtained for the poly(vinyl chloride) sample were found to be comparable to those reported for viscoelastic experiments over a broad temperature range above and below T_g carried out for different polymers. The origin of the decrease in enthalpy was briefly discussed in terms of the chain dynamics in the isothermal condition.     

Toward direct determination of conformations of protein building units from multidimensional NMR experiments III

Chemical shielding anisotropy tensors have been determined, within the GIAO-RHF formalism using a smaller [6-31+G(d)] and two medium-size basis sets [6-311++G(d,p) and TZ2P], for all elements of the conformational library (altogether 27 structures) of the hydrophobic model peptide For-L-Phe-NH₂. The individual chemical shifts and their conformational averages have been compared to their experimental counterparts taken from the BioMagnetic Resonance Bank (BMRB). At the highest level of theory applied, for all nuclei but the amide proton, deviations between statistically averaged theoretical and experimental chemical shifts are as low as a few percent. One-dimensional (1D) chemical shift - structure plots do not allow unambiguous identification of backbone conformations. On the other hand, on chemical shift - chemical shift plots of selected nuclei, e.g., ¹H ^N with ¹⁵N or ¹⁵N with ¹³C ^α , regions corresponding to major conformational motifs have been found, providing basis for the identification of peptide conformers solely from NMR shift data. The 2D ¹H ^α -¹³C ^α as well as the 3D ¹H ^α -¹³C ^α -¹³C ^β chemical shift - chemical shift plots appear to be of special importance for direct determination of conformations of protein building units from multidimensional NMR experiments. 48 pairs of ¹H ^α -¹³C ^α data for phenylalanine residues have been extracted from 18 selected proteins and compared to relevant ab initio results, supporting the calculated results. Thus, the appealing idea of establishing backbone folding information of peptides and proteins from chemical shift information alone, obtained from selected multiple-pulse NMR experiments (e.g., 2D-HSQC, 2D-HMQC, and 3D-HNCA), has received further support.     

Experimental calculations of number,energy and dose albedos for various materials using 662 keV gamma rays

ABSTRACT

Number, energy and dose albedos are measured at a scattering angle of 180° for a broad beam of 662 keV gamma rays obtained from a radioactive source of ¹³⁷Cs (having strength in µCi; 1 Ci?=?3.7?×?10¹⁰ disintegrations per second). The gamma beam is incident on semi-infinite thick targets of variable atomic numbers. The scattering media is divided into three sets, which are pure elements, alloys and composite materials. Experiments are carried out using a 3^″?×?3^″ NaI(Tl) scintillation detector. To obtain precision in data, the response unfolding of a scintillation detector is used, which converts the observed pulse-height distribution to a true photon spectrum over the energy range of 2.5 to 640 keV. The detector response unfolding results in the true intensity of back-scattered gamma flux by shifting the events resulting from partial absorption of photons to the full energy peak of the spectrum. In the present study, albedo factors are studied as a function of target thickness and their atomic number. The experimentally calculated numbers of back-scattered gamma photon are in good agreement with theoretically generated numbers of multiple back-scattered counts by using a Monte Carlo simulation code. The experimental data on energy and intensity of 662 keV gamma photons are used to evaluate the number, energy and dose albedos for different materials under investigation.     

About ageing and fading of Cr-39 PADC track detectors used as air radon concentration measurement devices

PADC detectors are widely used as air radon concentration measurement devices and the typical procedure that a Radon Service Laboratory uses to manage the detectors provides a calibration phase followed by the field measurement. The calibration is performed in a reference radon concentration atmosphere, using high radon concentration values in order to achieve typical exposure values of few MBq h m^?3 with an exposure time of few days. On the other hand the field measurement is characterized by long term exposures lasting up to six months and by radon concentrations that are quite lower than the ones used in the calibration.The aim of this study is to check whether the calibration procedure is actually representative of a field measurement, or, in other words, whether and how much ageing or fading can affect the calibration factor.We found that the ageing and fading effect can produce a decrease in the detector sensitivity leading to an underestimation of the radon concentration up to 40% for exposure lasting few months. An important issue is that both ageing and fading can be ascribed to a decrease in the track etching velocity V_t.In the paper we also provide an algorithm to compensate for the sensitivity variation due to fading/ageing effect.     

Fluorescence Study of the Relaxation Process in Excited Hetarylthiazole Cations

The absorption and fluorescence spectra of five cations protonated at the quinolyl nitrogen atom (IH⁺–VH⁺) and one ethylated (IEt⁺) cation were investigated. For these compounds (except VH⁺) both an anomalously large fluorescence Stokes shift (up to 238 nm) and a large short-wavelength fluorescence shift (up to 145 nm) at decreasing temperatures (down to 77 K) were observed. This is not the case for unprotonated molecules. The ground-state conjugation between quinolyl and another molecular fragment was found for II, IH⁺, IIH⁺, and IEt⁺. The relaxation process of excited cations is medium viscosity and temperature dependent. The experimental results are explained in terms of excited-state structural relaxation.     

Overhauser shift of the electron spin-resonance line of Si:P at the metal-insulator transition: II. 29 Si contribution

The electron-spin resonance (ESR) line of delocalised electrons shifts upon saturation due to the hyperfine interaction with the dynamically polarized nuclear spins. The ²⁹ Si part of the Overhauser shift of the ESR line of phosphorus doped silicon (Si:P) is separated in the concentration range 2.7 ... 7.3×10 ¹⁸ / cm ³ covering the metal-insulator transition. The Overhauser shift profiles, recorded versus ²⁹ Si nuclear magnetic resonance (NMR) frequency, are asymmetric. Their dependence on temperature and ESR saturation compares reasonably with simulations. Time and NMR frequency dependence of the dynamic nuclear polarization is studied in detail. No pronounced variation of the ²⁹ Si Overhauser shift profiles with P concentration is observed, but the maximum value of the shift profile decreases with increasing P concentration. In contrast to standard ²⁹ Si NMR results, these measurements reveal the behaviour of the ²⁹ Si nuclei close to the P doping sites. Received 8 November 2001     

Contribution to the research on cellulose diacetate as a solid state track detector

Abstract

While having a similar composition to Cellulose Triacetate, Cellulose Diacetate is a less sensible heavy ions detector. With a 0.9 N potash etching at 20°C, ions which have higher Z than Carbon are not recorded and the Etch Rate Ratio is about 1 to 2 for Cu and Kr ions. The study of the infrared absorption spectra shows a decrease of the v(O-H) band intensity at 3500 cm^?1 for CDA, when it increases for CTA.     

Development of a microstrip-based neutron detector

A gas-filled microstrip detector for thermal neutrons has been built and successfully tested in our laboratory. The detector has an active area of 20 mm × 15 mm and consists of alternate anodes and cathodes of widths 12 μm and 300 μm respectively. The anode to cathode gap is 150 μm and the pitch is 612 μm. A high resistance, meandering type horizontal strip connects the anodes at one end and aids in position sensing by charge division method. The detector is tested with gas mixtures³He+Kr (1: 2) and³He+CF₄ (2:1) at pressure of 3 atmospheres and using a Pu-Be neutron source. The pulse height spectrum shows energy resolution of ∼8% (FWHM) for the 764 keV peak at anode voltage of 525 V for³He+Kr and ∼15% at anode voltage of 800 V for³He+CF₄. Gas gains up to 6.3 × 103 and 3.6 × 103 are obtained respectively with these gas mixtures. The overall efficiency of the detector along the sensitive length is tested by exposing the active area to neutrons and recording the position spectrum. The detector shows fairly uniform efficiency (∼45%) over the active length.     

Spectroscopic Studies of a New Multi-Element Sensitive Fluorescent Probe Derived from 2-(2-pyridyl)benzimidazole: Selective Discrimination of Zn2+ from Its Congeners

ABSTRACT

A new multielement sensitive fluorescent probe, 1-(2-(phenylthio)ethyl)-2-(pyridin-2-yl)-1H-benzo[d]imidazole (L), has been synthesized by the reaction between 2-(pyridyl) benzimidazole and 2-chloroethyl phenyl sulfide. Excitation and emission wavelength of L are at 330 and 371 nm, respectively. Among various transition and nontransition metal ions, it can selectively read Zn²⁺ ion as the emission wavelength of L undergoes a red shift by 31 nm upon binding with Zn²⁺ in methanol. In the presence of Cd²⁺, Hg²⁺, and other common cations, the emission wavelength of L remains unchanged, and thus allows us to discriminate Zn²⁺ from its congeners. Both L and its Zn²⁺ complex are well characterized by different spectroscopic techniques like ¹H-NMR, ESI-TOF (+) mass, FT-IR, and elemental analysis data. The binding constant value of the complexation reaction between L and Zn²⁺ is found as 724.6 M^?1 in methanol. Density functional theoretical (DFT) studies nicely demonstrate the red shift in the emission wavelength of L upon binding with Zn^2+.     

CF3CDCl2分子红外多光子光热吸收谱

本文报道用铂丝光热吸收池作为探测器得到了CF₃CDCI₂的红外多光子吸收谱。并发现在线性吸收谱中944cm^-1处的吸收峰在多光子吸收谱中分裂为947cm^-1和927cm^-1两个吸收峰。这一现象与科里奥利力和非谐性引起的简正振动的耦合作用有关。这样,在用CF₃CDCI₂/CF₃CHCI₂体系分离氘同位素时,可以根据这一新结果选择更合适的激发波长。实验还发现在线性吸收谱中986cm^-1处的吸收峰在多光子吸收谱中出现约6cm^-2的红移。这种红移现象起源于分子振动能级的非谐性。 关键词：     

Sensitive and accurate dual-wavelength UV-VIS polarization detector for optical remote sensing of tropospheric aerosols

An UV-VIS polarization lidar has been designed and specified for monitoring aerosols in the troposphere, showing the ability to precisely address low particle depolarization ratios, in the range of a few percent. Non-spherical particle backscattering coefficients as low as 5×10^?8 m^?1?sr^?1 have been measured and the particle depolarization ratio detection limit is 0.6 %. This achievement is based on a well-designed detector with laser-specified optical components (polarizers, dichroic beamsplitters) summarized in a synthetic detector transfer matrix. Hence, systematic biases are drastically minimized. The detector matrix being diagonal, robust polarization calibration has been achieved under real atmospheric conditions. This UV-VIS polarization detector measures particle depolarization ratios over two orders of magnitude, from 0.6 up to 40 %, which is new, especially in the UV where molecular scattering is strong. Hence, a calibrated UV-VIS polarization-resolved time-altitude map is proposed for urban and free tropospheric aerosols up to altitude of 4 kilometers, which is also new. These sensitive and accurate UV-VIS polarization-resolved measurements enhance the spatial and time evolution of non-spherical tropospheric particles, even in urban polluted areas. This study shows the capability of polarization-resolved laser UV-VIS spectroscopy to specifically address the light backscattering by spherical and non-spherical tropospheric aerosols.     

Isotope shifts and hyperfine structure in the transitions of gadolinium

High-resolution resonance ionization mass spectrometry has been used to measure isotope shifts and hyperfine structure in all (J = 2-6) and the transitions of gadolinium (Gd I). Gadolinium atoms in an atomic beam were excited with a tunable single-frequency laser in the wavelength range of 422-429 nm. Resonant excitation was followed by photoionization with the 363.8 nm line of an argon ion laser and resulting ions were mass separated and detected with a quadrupole mass spectrometer. Isotope shifts for all stable gadolinium isotopes in these transitions have been measured for the first time. Additionally, the hyperfine structure constants of the upper states have been derived for the isotopes ^{155, 157} Gd and are compared with previous work. Using prior experimental values for the mean nuclear charge radii, derived from the combination of muonic atoms and electron scattering data, field shift and specific mass shift coefficients for the investigated transitions have been determined and nuclear charge parameters for the minor isotopes ^{152, 154} Gd have been calculated. Received 18 November 1999     

Effects of Gd<Superscript>3+</Superscript> doping on structural and dielectric properties of PZT (Zr:Ti = 52:48) piezoceramics

The purpose of this research is to study the effect of doping Gd into Pb(Zr_0.52Ti_0.48)O₃ ceramics prepared by solid state reaction. X-ray diffraction patterns show that all PGZT samples are of tetragonal structure and the highest doping should be no more than 2 mole % Gd at which the unreacted oxides start to appear. The electron spin resonance (ESR) spectra of PGZT's indicate that Gd³⁺ can enter both A site of the perovskite structure instead of only A site as widely believed. The ESR peaks resonance shift towards low fields as the concentration is higher, which is due to the change in crystal field experienced by Gd³⁺ ions. At x =0.001, 0.005 and 0.01 dopings, two sets of powder ESR signals arising from Gd³⁺ (4f⁷, spin 7/2) ions at A site. The first set shows some fine structure having strong absorption peaks centered at 76.26 mT (g = 8.550). The second is a seven-peak spectrum centered at 206.01 mT (g = 3.165), which belongs to the Gd³⁺ ions at B sites. Furthermore, the overlapped ESR strong absorption peaks from 309.17 mT to 314.49 mT (g = 2.2818-2.1087) belong to Gd³⁺ of unreacted Gd₂O₃. The local environments of Gd³⁺ ions were verified from the calculated ESR spectra using appropriate spin Hamiltonian parameter, i.e. gyromagnetic tensor g, zero-field splitting D and hyperfine tensor A.     

The Electronic and Infrared Absorption Spectra of Toluene-d

Abstract

The infrared and ultraviolet absorption spectra of toluene-d have been investigated for the first time in the regions 400 - 4000 cm^?1 and 2350 ?2750 A° respectively. The intense band at 2666.3 A°(37494 cm^?1) in the u.v. vapour absorption spectrum has been identified as the o,o band and others have been interpreted in terms of the three (519,632 and 785 cm^?1) ground state and the six (454,526,743,935,963 and 1180 cm^?1 excited state fundamentals. The correlation of the various frequencies of the ground and excited states of toluene and toluene-d has been done. The observed isotopic shift for toluene-d is 14 cm^?1.     

Isotope shift studies in the first spectrum of dysprosium: confirmation of assignments to and new assignments to configuration

Isotope shifts (-) are reported for 221 spectral lines of the neutral dysprosium atom (Dy I) in the region 470-565 nm using a photoelectric recording Fabry-Perot spectrometer and highly enriched isotopic samples of and excited in liquid-nitrogen-cooled hollow-cathode lamps. Isotope shift data for 173 of these lines are being reported for the first time. Using the isotope shift data, term isotope shifts (-) have been evaluated for 99 even- and 68 odd-parity energy levels of Dy I. New values have been obtained for 24 odd and 36 even levels. These new values have enabled us to check some of the existing tentative assignments and also to suggest configuration assignments to a few unassigned energy levels. The earlier tentative assignments of 4 f10 5 d 6 p configuration to many high odd levels lying above have been presently confirmed. We could assign the 4f^95d6s6p configuration to 24 unassigned even levels. Received: 3 August 1998