Nature of oxygen in the passive film on stainless steels in 0.1 M NaCl solution

Three different oxygen species, O^2–, OH^–, and H₂O, are introduced into the deconvolution of the oxygen peaks measured in the prior study and their true concentrations are investigated in the depth profile. It is found that H₂O exists mainly in the outermost part of the passive film at the interface of solution and the passive film. OH^– and O^2– are found throughout the passive film; they have a maximum concentration in the outer layer at around 10 to 20 Å depth, with a concentration of 40 at.% for the stainless steel 29-4-2 and 50 at.% for 18-12. After the maximum the concentrations are sharply reduced with increasing sputtering time and remain at a constant concentration of about 10 at.% at 35 Å depth. Both species still exist at this concentration even after long time sputtering.     

Application of high-frequency ultrasound standing waves for the recovery of lipids from high-fat dairy effluent

Effect of high-frequency ultrasonication was examined on wastewater of a cheese manufacturing plant. Tests were carried out at two frequencies (500 kHz and 1 MHz) and two temperatures (22 and 40 °C). Samples were subjected to different energy densities; 7.5, 30.2, 60.5 and 121.0 J/mL at 500 kHz and 7.9, 31.7, 63.4 and 126.8 J/mL at 1 MHz to observe the creaming and recovery of lipid. These energy densities correspond to 30, 120, 240 and 480 s of sonication. Sonication was performed using a single plate transducer and reflector system at 40 W to create standing wave to coalesce and flocculate lipid globules. Recovery was higher at 40 °C after 480 s of sonication at both frequencies (77% at 500 kHz and 75% at 1 MHz). The lowest recovery of 47% was observed at 500 kHz and 22 °C at all applied energy densities. Changes in particle size and turbidity in the bottom aliquot indicated that high-frequency ultrasound caused coagulation and aggregation and settling of colloidal particles. Increase in particle size was observed to be highest at 1 MHz, 40 °C and 480 s of sonication. These results confirm that high-frequency ultrasound standing wave technology can be used to recover lipid from high-lipid dairy wastewater including that from cheese manufacturing.     

Analysis of the effect of annealing on the photoluminescence spectra of Cu ion implanted ZnS nanoparticles

In the present study, we report the photoluminescence (PL) study of nanoparticles of ZnS implanted with Cu⁺ ions at the doses of 5×10¹⁴, 1×10¹⁵ and 5×10¹⁵ ions/cm² and annealed at 200 and 300 °C. The photoluminescence spectra of the samples implanted at lower doses of 5×10¹⁴ and 1×10¹⁵ ions/cm² and annealed at 200 and 300 °C showed peaks at around 406, 418 and 485 nm. The PL emission peak at 485 nm was attributed to the transition of electrons from conduction band of ZnS to the impurity level formed by the implanted Cu⁺ ions. In the PL spectrum of the sample implanted at the highest dose of 5×10¹⁵ ions/cm², in addition to the emission peaks observed in the PL spectra of the samples implanted at lower doses, a peak at around 525 nm, the intensity of which decreased with increase in the annealing temperature, was observed. The emission peak at 525 nm was attributed to the transitions between sulfur and zinc vacancy levels. The full width at half maximum (FWHM) of the emission peak at 406 nm was observed to decrease with increase in annealing temperature, indicating lattice reconstruction. The observation of copper ion impurity related peak at 485 nm in the PL spectra of samples of the present study indicated that the doping of copper ions into the ZnS lattice is achievable by implanting Cu⁺ ions followed by annealing.     

Multi-peak behavior of photoluminescence of silica particles heat-treated in hydrogen at elevated temperature

Pure nano-partical silica was prepared by sol-gel method, and then was treated in a H₂ ambient at different temperatures. The surface structure and valence bonding of samples were analyzed with IR spectrum and X-ray induced photoelectron spectroscopy, respectively. Its photoluminescence property was studied with fluorescence spectroscopy. The results showed that only one luminescence band at 344 nm exists for silica heat-treated at 450 °C. Silica samples heat-treated at higher temperatures showed completely different luminescence comparing with the samples heat-treated at lower temperatures. Multi-peaks were found in the SiO₂ samples heat-treated at temperatures higher than 700 °C, in which the luminescence peaks at about 379 and 392 nm are similar with the β bands in silica glass originated from the same defect center of two-fold coordinated silicon atoms, and the luminescence bands at about 493 and 528 nm are few reported. The intensity of the luminescence bands increase with the increase of heat treatment temperature from 700 to 900 °C.     

15N allocation into wheat grains (Triticum aestivum L.) influenced by sowing rate and water supply at flowering under a Mediterranean climate

This study examined the effects of a reduced wheat sowing rate (250 vs. 500 grains m^–2) on grain yield, uptake of ¹⁵N into grains, and the incorporation into gluten and non-gluten proteins of wheat under field conditions in the Aegean region. A single ¹⁵N application was applied at stem elongation, at flowering, or at both developmental stages. Each ¹⁵N treatment included either additional water supply, or no additional water supply at flowering. Sowing rate (either 250 or 500 grains m^–2) had no impact on grain yield. Grain yield increased with additional water supply, but at the expense of protein quality, because of a decrease in the protein content of gluten. The ¹⁵N content of the gluten and non-gluten proteins at grain maturity was not different among cultivars. ¹⁵N applied at both stem elongation and flowering was found in comparable amounts in grains and protein fractions, irrespective of sowing rate.     

Moderate hydrostatic pressure–temperature combinations for inactivation of Bacillus subtilis spores

We report the effect of using moderate hydrostatic pressure, 40–140?MPa, at moderate temperature (38–58°C) to inactivate Bacillus subtilis spores in McIlvaine's citric phosphate buffer at pH 6. We have investigated several parameters: pressure applied, holding time, pressure cycling, and temperature. The kinetics of spore inactivation is reported. The results show that spore inactivation is exponentially proportional to the time the sample is exposed to pressure. Spore germination and inactivation occur at the hydrostatic pressures/temperature combinations we explored. Cycling the pressure while keeping the total time at high pressure constant does not significantly increase spore inactivation. We show that temperature increases spore inactivation at two different rates; a slow rate below 33°C, and at a more rapid rate at higher temperatures. Increasing pressure leads to an increase in spore inactivation below 95?MPa; however, further increases in pressure give a similar rate kill. The time dependence of the effect of pressure is consistent with the first-order model (R²?>?0.9). The thermal resistance values (Z_T) of B. subtilis spores are 30°C, 37°C, and 40°C at 60, 80, 100?MPa. The increase in Z_T value at higher pressures indicates lower temperature sensitivity. The pressure resistance values (Z_P) are 125, 125 and 143?MPa at 38°C, 48°C, and 58°C. These Z_P values are lower than those reported for B. subtilis spores in the literature, which indicates higher sensitivity at pressures less than about 140?MPa. We show that at temperatures <60°C, B. subtilis spores are inactivated at pressures below 100?MPa. This finding could have implications for the design of the sterilization equipment.     

The half-life of <Superscript>198</Superscript>Au : High-precision measurement shows no temperature dependence

We have measured the half-life of the β -decay of ¹⁹⁸Au in a metallic environment, both at low temperature (19K), and also at room temperature. We find the half-lives at both temperatures to be the same within 0.04%, a finding that contradicts a recent report of a 3.6±1.0 % difference in the ¹⁹⁸Au half-life when measured at essentially the same two temperatures. Our results for the half-life, 2.6949±0.0009 d at room temperature and 2.6953±0.0008 d at 19K, also agree well with previous precision room temperature measurements.     

Re-dispersible Li<Superscript>+</Superscript> and Eu<Superscript>3+</Superscript> co-doped CdS nanoparticles: Luminescence studies

Re-dispersible CdS, 5 at.% Eu³⁺-doped CdS, 2 at.% Li⁺ and 5 at.% Eu³⁺ co-doped CdS nanoparticles in organic solvent are prepared by urea hydrolysis in ethylene glycol medium at a low temperature of 170°C. CdS nanoparticles have spherical shape with a diameter of ∼80 nm. The asymmetric ratio (A ₂₁) of the integrated intensities of the electrical dipole transition to the magnetic dipole transition for 5 at.% Eu³⁺-doped CdS is found to be 3.8 and this ratio is significantly decreased for 2 at.% Li⁺ and 5 at.% Eu³⁺ co-doped CdS (A ₂₁ = 2.6). It establishes that the symmetry environment of Eu³⁺ ion is more favored by Li-doping. Extra peak at 550 nm (green emission) could be seen for 2 and 5 at.% Eu³⁺ co-doped CdS. Also, the significant energy transfer from host CdS to Eu³⁺ is found for 5 at.% Eu³⁺-doped CdS compared to that for 2 at.% Li⁺ and 5 at.% Eu³⁺ co-doped CdS.      

Optical properties of a 5 m echelle vacuum spectrometer with an approximately diffraction-limited resolving power in the order of 106

The image formation and the spectral resolution of a 5m echelle spectrometer were investigated. As shown in this study, the spectrometer operates approximately diffraction-limited in the visible and uv, whereas in the vacuum uv (120.0 nm) the resolving power is still >54% of the diffraction-limited value. The spectrometer was designed according to the results of an analytical imaging theory. Residual optical aberrations were investigated by measuring the image distributions at four wavelengths between 120.0 and 632.8 nm (grating replaced by a plane mirror), in order to experimentally test the reliability of these theoretical results in combination with the influence of the imperfections of the optical components. The ratios of 40%-widths of the measured image distributions in the exit slit plane to the corresponding theoretical values were determined to be 0.56 at 120.0 nm, 0.68 at 174.0 nm, 0.74 at 257.3 nm, and 0.99 at 632.8 nm. Due to a lack of suitable light sources in the vacuum uv with sufficiently small band widths, the instrumental functions of the spectrometer could only be measured at 257.3, at 514.5, and at 632.8 nm, using stabilized and frequency doubled laser lines. The resolving powersR, which were deduced from the 40%-widths of the measured instrumental functions, were determined to be 1.42×10⁶ [0.80] at 257.3 nm, 0.86×10⁶ [0.97] at 514.5 nm, and 0.71×10⁶ [0.98] at 632.8nm (ratiosR ^exp/R ^theor in brackets). The comparatively high resolving powerR≳0.02×10⁶ [0.54] at 120.0 nm was estimated from the 40%-width of the measured image distribution.     

注入Ar+的蓝宝石晶体退火前后光致发光谱的分析

对注入Ar⁺后不同晶面取向的蓝宝石晶体在不同退火条件下的光致发光谱进行了分析.分析结果表明:三种晶面取向的蓝宝石样品经Ar⁺注入后,其光致发光谱中均出现了新的位于506nm处的发光峰;真空和空气气氛下的退火均对样品在506nm处的发光有增强作用,不同晶面取向的样品发光增强程度不同,且发光增强至最大时的退火温度也不同,空气气氛下的退火使样品发光增强程度更为显著.由此可以看出,退火气氛、退火温度和晶面取向均对样品发光峰强度有影响. 关键词： 2O₃')" href="#">Al₂O₃ 离子注入 退火 光致发光谱     

Wavelength dependent resonant nonlinearities in a standard saturable absorber IR26 on picosecond time scale

Nonlinear optical properties of a standard dye IR26 have been studied by using the Z-scan technique to decipher the difference in the mechanism of nonlinear absorption on picosecond time scale at two wavelengths i.e. at 1064 nm and 532 nm. A prominent contribution of nonlinear absorption is observed in the Z-scan profiles at 1064 nm. The dye exhibits the mechanism of self-defocusing at 1064 nm in contrast to that of self-focusing at 532 nm. While the two photon absorption has been found to be the dominant mechanism of reverse saturable absorption at 1064 nm, the mechanism of excited state absorption is operating at 532 nm. Additionally, the optical phase conjugate geometry of degenerate four wave mixing (DFWM) technique has been used to measure the third order nonlinear susceptibility values at 532 nm to compare with those obtained from the Z-scan profiles.     

μ+ shift study inCdMgx (x=1%, 2%, 2.5%)shift study inCdMgx (x=1%, 2%, 2.5%)

In continuation of our earlier studies of the anomalous temperature dependence of the μ⁺ Knight shift K_μ in Cd,CdHg (1.2 at %) andCdMg (3.38 at %) — interpreted as due to Van Hove-type singularities in the local density of electron states /1/ — we have studied the temperature dependence of the μ⁺ Knight shift in polycrystallineCdMg (1.04 at %, 2.05 at %) and in a single crystal ofCdMg (2.5 at %). In contrast to pure Cd no anisotropies in K_μ could be detected. The temperature dependence of K_μ in aCdMg (2.05 at %) sample and in the monocrystallineCdMg (2.5 at %) sample essentially reproduces the one previously observed in polycrystallineCdMg (3.38 at %), showing a steplike discontinuity and a logarithmic singularity. A complete different behaviour is observed inCdMg (1.04 at %), where no logarithmic singularity seems to show up and where a steplike discontinuity of opposite sign at around 90 K is clearly seen. If these singularities are still to be interpreted in terms of Van Hove singularities, the question arises why there is such a nonlinear dependence on the Mg concentration.     

Blue up-conversion with excitation into Tm ions at 808 nm in YVO4 crystals co-doped with thulium and ytterbium

The up-conversion of infrared radiation at 808 nm, emitted by a diode laser, into blue emission centered at 480 nm in 1 at.% Tm, 5 at.% Yb: YVO₄; 1 at.% Tm, 8 at.% Yb: YVO₄ and 2 at.% Tm, 5 at.% Yb: YVO₄ has been studied. The highest intensity of blue emission is found for the 1 at.% Tm, 8 at.%Yb: YVO₄ system. The power dependence of up-converted emission upon continuous-wave excitation as well as the time evolution of its intensity upon short-pulse excitation were found to be consistent with a two-step excitation mechanism in which the forward Tm³⁺–Yb³⁺ energy transfer is followed by the back Yb³⁺–Tm³⁺ energy transfer. The effect of dopant concentrations on the up-conversion process is interpreted taking into account dynamics of the excited states involved.     

Two-dimensional multiplicity fluctuation analysis of target residues in nuclear collisions

Multiplicity fluctuation of the target residues emitted in the interactions in a wide range of projectile energies from 500 A MeV to 60 A GeV is investigated in the framework of two-dimensional scaled factorial moment methodology.The evidence of non-statistical multiplicity fluctuation is found in 16 O-AgBr collisions at 60 A GeV,but not in 56 Fe-AgBr collisions at 500 A MeV,84 Kr-AgBr collisions at 1.7 A GeV,16 O-AgBr collisions at 3.7 A GeV and 197 Au-AgBr collisions at 10.7 A GeV.     

A metastable de-excitation spectroscopy (MDS) study on oxygen adsorption on a polycrystalline zirconium surface

The adsorption of oxygen on a polycrystalline zirconium surface at room temperature has been studied by metastable de-excitation spectroscopy (MDS) in conjunction with UPS and AES. From the analysis of the measured spectra, we have shown the following. (1) At the initial stage of oxygen adsorption (exposure <1.2 L), the surface density of states (SDOS) of zirconium changes little at around the Fermi level (E_F), while it decreases appreciably at 1–2 eV below E_F (E_B=1–2 eV) by oxygen adsorption. (2) The SDOS at E_B=0–2 eV decreases with increasing oxygen exposure at >1.2 L and disappears at >8 L. (3) The oxygen 2p states (E_B=5–8 eV) are localized at the subsurface region at oxygen exposure 0–2 L. (4) The ZrO₂ phase appears at the outermost zirconium surface at around 2 L, then grows with increasing exposure, and finally dominates at >8 L. It is suggested that two different phases (ZrO₂ phase and that in which oxygen occupies subsurface sites) coexist at the outermost surface at 2–8 L.     

Luminescence centers in ceramics of yttrium, scandium, and bismuth oxytungstates

An investigation is made of the luminescence spectra of Me₂WO₆ ceramics (Me=Y, Sc, Bi). The spectra were decomposed into elementary components by the Alentsev—Fock method. Radiation hands with a maximum at 3.02 eV in the Y₂WO₆ luminescence spectrum, at 2.8 eV in the ScWO₆ spectrum, and at 2.93 eV in the Bi₂WO₆ spectrum are assigned to the light emission of self-localized Frenkel excitons. The bands with maxima at 2.25 and 1.75 eV in the Y₂WO₆ spectrum, at 2.36 and 1.9 eV in the Sc₂WO₆ spectrum, and at 2.35 and 1.9 eV in the Bi₂WO₆ spectrum are related to oxygen vacancies. Translated from Zhurnal Prikladnoi Spektroskopii, Vol 67, No. 2, pp. 273–275, March–April, 2000.     

Pressure-induced molecular dissociation in iodine at low temperatures

Abstract

Synchrotron x-ray diffraction experiments at low temperatures have revealed that even at 35K the molecular dissociation starts taking place at P_S=21.5 and finishes at P_f=26.1GPa. An extrapolation of the phase boundary thus obtained at several temperatures intersects the T=4K line at P_S=21.6 and P_f=26.3GPa. This result, inferring the monatomic structure to be realized at P=30GPa and T=4K, leads to a discrepancy against the recent Mössbauer result obtained at the same point in the P-T phase diagram.     

Microstructure, hydrogenation and optical behavior of Mg-Ni multilayer films deposited by magnetron sputtering

Mg-Ni multilayer films with sequential Mg and Ni layers were prepared by direct current magnetron sputtering. The substrate temperature influences the microstructure of the films greatly. The film deposited at 298 K exhibits multilayered structure, while the film shows nanocrystalline/amorphous composite structure at the deposition temperature of 473 K. The optical properties between hydrogenation/dehydrogenation states of the films were performed using spectrophotometer in visible light region. The film deposited at 473 K can switch from mirror-like metallic state towards brownish yellow transparent state under 0.6 MPa H₂ at 298 K, and the optical transmittance modulation reaches up to 20% both at a wavelength of 770 nm and IR region, while the film deposited at 298 K exhibits low optical change, and the optical switching behavior can hardly be found. The extra free energy stored in the boundary of the nanocrystallines benefits the formation of magnesium-based hydride, resulting in the enhancement of the optical switching properties of the Mg-Ni film deposited at 473 K.     

Generation of microcellular poly(methyl methacrylate) by compressed gases

Abstract

Generation of microcellular poly(methy1 methacrylate) (PMMA) was studied in CO₂ and N₂O at pressures from 2 to 15MPa at three temperatures, 293.2K, 308.2K, and 323.2 K. The average diameter d and average number density N of voids generated by a rapid expansion of compressed gases in PMMA were measured by use of an optical microscope. Effects of gases, temperature, and pressure on the d and N values were examined. Even at pressure below glass transition pressure of PMMA with both gases, voids of diameter being as small as those found at high pressure, 15MPa, were obtained at each temperature. However, the void density of PMMA at lower pressure by both gases was not so good as those obtained at high pressures.     

Absorption,excitation and fluorescence spectra of thallium activated cesium bromide

Absorption, excitation and fluorescence spectra of T1⁺ doped cesium bromide have been investigated at various thallium concentrations. At very low thallium concentration two absorption bands are obtained at 225 nm and 264 nm. With rise of thallium concentration additional absorption bands are obtained at 230, 244, 258, 270 and 285 nm. A single bell-shaped fluorescence band at 357 nm in the ultraviolet region is obtained at low thallium concentration. Two additional visible fluorescence bands appear at 440 and 540 nm with rise in thallium content. The excitation spectra for ultraviolet emission band and visible emission bands are found to be different. Accordingly the ultraviolet emission band is attributed to the characteristic A emission in T1⁺ ion and the visible bands are attributed to dimer centers havingD _4h site symmetry.