β-decay matrix elements from the study of asymmetric emission from polarised nuclei: γ-tagging – a new method for complex β-decay

A new method is introduced designed to facilitate study of matrix elements in complex β-decay through the measurement of asymmetric β-emission from a low-temperature polarised source. The method involves coincident detection of the β-emission with subsequent γ-transitions to tag the β-spectrum component. The method is demonstrated by application to the decay of ¹⁴⁰La. This revised version was published online in August 2006 with corrections to the Cover Date.     

Measurement of the sizes of a source of α particles from the collisions of relativistic 22Ne and 24Mg nuclei with photoemulsion nuclei

The correlation of two α particles has been measured. In the case of a one-dimensional parameterization of the correlation function, the size of the source of the α particles is R(α) = 2.84 ± 0.28_stat ± 0.23_sist fm. This result is compared to similar measurements for protons and deuterons.     

Normal and excess nitrogen uptake by iron-based Fe–Cr–Al alloys: the role of the Cr/Al atomic ratio

Upon nitriding ferritic iron-based Fe–Cr–Al alloys, containing a total of 1.50 at. % (Cr?+?Al) alloying elements with varying Cr/Al atomic ratio (0.21–2.00), excess nitrogen uptake occurred, i.e. more nitrogen was incorporated in the specimens than compatible with only inner nitride formation and equilibrium nitrogen solubility of the unstrained ferrite matrix. The amount of excess nitrogen increased with decreasing Cr/Al atomic ratio. The microstructure of the nitrided zone was investigated by X-ray diffraction, electron probe microanalysis, transmission electron microscopy and electron energy loss spectroscopy. Metastable, fine platelet-type, mixed Cr_{1? x} Al _x N nitride precipitates developed in the nitrided zone for all of the investigated specimens. The degree of coherency of the nitride precipitates with the surrounding ferrite matrix is discussed in view of the anisotropy of the misfit. Analysis of nitrogen-absorption isotherms, recorded after subsequent pre- and de-nitriding treatments, allowed quantitative differentiation of different types of nitrogen taken up. The amounts of the different types of excess nitrogen as function of the Cr/Al atomic ratio are discussed in terms of the nitride/matrix misfit and the different chemical affinities of Cr and Al for N. The strikingly different nitriding behaviors of Fe–Cr–Al and Fe–Cr–Ti alloys could be explained on this basis.     

Effect of Fe,Co, Ni and Cd CO‒activation on luminescence emission and decay of CaS:Ce phosphors

Cathodoluminescence (CL), photoluminescence (PL), thermoluminescence (TL) spectra, and decay after laser beam excitation of cerium-activated CaS phosphors doped with Fe, Co, Ni or Cd have been investigated. These studies shed some light on the nature of luminescence centres and the association of various groups of traps with the dopants. Effect of concentiation variation of these four elements on emission and decay characteristics of CaS:Ce phosphor has been discussed. In contrast with the earlier publication [W. Lehmann and F. M. Ryan, J. Electrochem. Soc. 119, 275 (1972)] we have found that Ni is an effective killer, Cd ineffective and Co has no clearly observable effect. Fe has also been found to be an effective killer for CaS:Ce phosphors. Ni and Fe appear to be more effective quenchers for shorter wavelength emission band characteristic of Ce in CaS.     

De–excitation of compound nuclei with A around 56: reduction of the emission barriers for protons and alpha particles

This paper contributes to the discussion on the phenomena of the enhanced emission of low–energetic charged particles during compound nuclei decay. The decay of compound nuclei ⁵²Fe, ⁵⁶Ni, and ⁵⁹Cu was studied. Energy spectra and emission angles of evaporated charged particles were measured in coincidence with gamma rays to determine the corresponding evaporation residue nucleus. Additionally, evaporation residue distributions were determined with the Munich rf recoil spectrometer. In this way, detailed channel–specific evaporation data were obtained for theoretical analysis. We extracted evaporation barriers and compared them with corresponding fusion barriers. The main result was revealed to be a lowering of the evaporation barrier for protons and alpha particles relative to the fusion barriers. But the observed effect is not as intensive as reported in recent studies. Received: 15 June 1998 / Revised version: 5 November 1998     

Reconstruction of all-electron orbitals from one-electron pseudowave functions and calculations of the intensities of Si X-ray emission spectra of Si, β-SiC,stishovite, and β-cristobalite crystals

The intensities of Si X-ray emission spectra of Si, β-SiC, stishovite, and β-cristobalite crystals are calculated. The wave functions of the initial and final states are obtained in the framework of the density-functional theory with the use of the norm-conserving and ultrasoft pseudopotentials. The all-electron crystal orbitals are reconstructed from the one-electron pseudowave functions. The probabilities of X-ray emission transitions are calculated by reconstructing the all-electron orbitals in two different gauges, namely, the length and velocity gauges. The calculated intensities are compared with the experimental spectra and the partial densities of states.     

Application of the multireference equation of motion coupled cluster method,including spin–orbit coupling,to the atomic spectra of Cr,Mn, Fe and Co

The recently introduced multireference equation of motion (MR-EOM) approach is combined with a simple treatment of spin–orbit coupling, as implemented in the ORCA program. The resulting multireference equation of motion spin–orbit coupling (MR-EOM-SOC) approach is applied to the first-row transition metal atoms Cr, Mn, Fe and Co, for which experimental data are readily available. Using the MR-EOM-SOC approach, the splittings in each L-S multiplet can be accurately assessed (root mean square (RMS) errors of about 70 cm^?1). The RMS errors for J-specific excitation energies range from 414 to 783 cm^?1 and are comparable to previously reported J-averaged MR-EOM results using the ACESII program. The MR-EOM approach is highly efficient. A typical MR-EOM calculation of a full spin–orbit spectrum takes about 2 CPU hours on a single processor of a 12-core node, consisting of Intel XEON 2.93 GHz CPUs with 12.3 MB of shared cache memory.     

Electron emission from Al,Pt, Ag,and Au surfaces under the action of resonant photons with λ=2537 and 1850 Å

An original variant of an electronic device is described, which can be used for gamma-process selection under ionized gas conditions. The device is based on a Hanley and Schaffernicht electron gun. Selection of photons and metastable atoms is performed by a quartz tube located in axial symmetry with the primary electron gun. The desired signal is measured from the flow of secondary electrons emitted from Al, Pt, Ag, and Au surfaces under the action of resonant photons radiated from the levels Hg(6³P₁) and Hg(6¹P₁). For =2537 Å the following values were obtained for _ph 9.1, 3.8, 1.1, 0.25. Analogous values of _ph for =1850 Å were equal to 45.5, 10.8, 6.5, 3.2. The _ph values are in units of 10^–4.Translated from Vysshikh Uchebnykh Zavedenii, Fizika, No. 12, pp. 68–74, December, 1987.     

Direct generation of 81 nJ pulses and external compression to a subpicosecond regime with a 4.9 MHz chirped-pulse multipass-cavity Cr⁴⁺:forsterite oscillator

We report direct generation of 81 nJ chirped pulses from a room-temperature, Kerr lens mode-locked Cr??:forsterite oscillator operating at 1258 nm. To increase the pulse energy, the pulse repetition rate of the short x-type resonator was lowered from 143 to 4.9 MHz by the addition of a q-preserving multipass cavity, which provided an additional effective optical path length of 59.4 m. The duration of the chirped pulses was around 5.5 ps with a spectral width of 21 nm. The pulses were externally compressed to 607 fs by using a diffraction grating pair. To our knowledge, this is the highest reported pulse energy directly generated from a room-temperature mode-locked Cr??:forsterite laser.     

Ordering effect on the mechanical,electronic and magnetic properties of the β-based non-canonical approximant phases: β-Al50Cu33Fe17, η-Al50Cu44Fe6 and φ-Al47.5Cu49.5Fe3

Abstract

Using transmission electron microscopy and X-ray diffraction, we established that the ordered η1-Al₅₀Cu₄₄Fe₆ and φ-Al_47.5Cu_49.5Fe₃ (Fmm2) alloys with nano-sized domain structure are formed by slowly cooling, whereas β-solid solutions with a short-range order were found in quenched states. The φ′-modification which exhibits the additional long-period superstructure was also observed in Al_47.5Cu_49.5Fe₃. The studies of low temperature magnetic susceptibility and heat capacity did not reveal any another phase transitions in these alloys. The indentation test showed that hardness and Young’s modulus consistently grow as β-Al₅₀Cu₃₃Fe₁₇ → η1-Al₅₀Cu₄₄Fe₆ → (φ+φ′)-Al_47.5Cu_49.5Fe₃ and approach to those in icosahedral phase. The same trend in the Young’s modulus was obtained for alloys containing β-solid solution with a short-range order. Ab initio calculations, however, predicted the opposite tendency in cubic β-Al₅₀Cu_50?xFe_x with a decrease in x, which was explained by the weakening of the covalent Fe 3d – Al sp bonding. This discrepancy between the results for β- and ordered phases, we related to a crucial effect of ordering which is accompanied by a progressive distortion of cubic local structure in the series β-Al₅₀Cu₃₃Fe₁₇ → η1-Al₅₀Cu₄₄Fe₆ → φ-Al_47.5Cu_49.5Fe_3. As we demonstrated for η-Al(Cu, Fe), these distortions lead to the strengthening of the both covalent Fe–Al and Cu–Al bonds and the higher modules.     

Formation of [3]Pseudorotaxanes from β-cyclodextrin and a Series of Dicarboxylic Acids with Their Corresponding α,ω-alkanedicarboxylate Anions

通过研磨法和共沉淀法成功制得β-环糊精与碳原子数11~15的脂肪族二元酸包合物,并通过傅立叶变换红外光谱(FTIR)、差热分析(DTA)以及X射线衍射(XRD)的方法确证了该包合物为[3]准轮烷结构．上述包合物通过与NaOH作用得到了β-环糊精与脂肪族二元酸双负离子的包合物并通过核磁共振氢谱(1H-NMR)及二维NOSEY谱确认了该包合物同样具有[3]准轮烷结构．     

A Spectroscopic Study of the Interaction of the Fluorescent β-Carboline-3-carboxylic Acid N-methylamide with DNA Constituents: Nucleobases, Nucleosides and Nucleotides

Interaction between beta-carboline-3-carboxylic acid N-methylamide, betaCMAM, and nucleobases, nucleosides and nucleotides is studied in the ground state with UV-visible, (1)H NMR and (31)P NMR spectroscopies and in the first excited state, with steady-state and time-resolved fluorescence spectroscopy. Job plots show a predominant 1:1 interaction in both electronic states. Association constants are estimated from changes in the absorption spectra, and show that the strongest interaction is produced with the nucleosides: 2'-deoxyadenosine (dAdo) and thymidine (Thd), and with the mononucleotides: 2'-deoxycytidine 5'- monophosphate (5'-dCMP) and uridine 5'- monophosphate (5'-UMP). These results are corroborated by the upfield shifts of two (1)H NMR resonances of the betaCMAM indole group. The (31)P NMR resonance of nucleotides is shifted downfield, suggesting the presence of electrostatic or hydrogen bond interaction with betaCMAM. In the first electronic singlet excited state, static and dynamic quenching of betaCMAM emission is achieved upon addition of nucleobases, nucleosides and nucleotides. This has been analysed using Stern-Volmer kinetics.     

Structure and Magnetic Properties of (Ni1 – xZnx)Fe2O4 Ceramics with a Spatial Change in the Composition

Physics of the Solid State - Samples of homogeneous (x = 0, 0.1, and 0.2) and multilayer ceramics based on solid solutions of nickel–zinc ferrites (Ni1 – xZnx)Fe2O4...     

Magnetic nanoparticles based on iron coated carbon produced from the reaction of Fe2O3 with CH4: a Mössbauer study

In this work, it was investigated the production of magnetic nanoparticles encapsulated with carbon by the reaction of hematite and methane by Temperature Programmed Reaction up to 950°C. XRD and Mössbauer analyses showed that the materials prepared at 600°C and 700°C are mainly composed of magnetite and small amounts of hematite α -Fe₂O₃ with particle size of 30–40 nm. At higher temperatures, the spectra also display two central doublets corresponding to wüstite phase (Fe_1???x O). The materials were also characterized by magnetization measurements, BET surface area, thermal analysis (TG) and SEM. These materials can be prepared by a simple and low cost process and show great potential to be used as adsorbents and catalyst support.     

Superconducting and electronic properties of the metallic glass system La75Si25−x M x (M=Cr,Mn, Fe,Co, Ni,Cu, B,Al, Ga,In)

A new ternary metallic glass system, La₇₅Si_25–x M _x (where M is a 3d or a IIIA element) has been prepared by melt spinning. The superconducting transition temperature,T _c , is depressed by the magnetic 3d elements. For low Fe concentrations (less than 5 at.%) the depression is about 0.3 K/at.%. Part of the depression may be explained by a decreased density of states atE _F as determined by UPS measurements. The strongest depression is associated with the magnetic pair breaking due to spin scattering. In the IIIA additions we correlateT _c with the atomic radius of the additive.     

Interatomic bonds and the tensile anisotropy of trialuminides in the elastic limit: a density functional study for Al3(Sc,Ti, V,Cr)

The tensile anisotropy in the elastic limit of Al₃(Sc,?Ti,?V,?Cr) intermetallic compounds in both the L1₂ and D0₂₂ crystal structure has been investigated using first-principles density-functional calculations. In both crystal structures the main bonding character comes from the saturation of dominant d ³ (L1₂) and d ⁴ (D0₂₂) hybrid orbitals located on the TM atoms. The series Al₃Sc?→ Al₃V corresponds to gradual d-band filling and leads to a gradual increase of bond-strength and covalent bond formation. The magnetism of Cr breaks this trend in the Al₃Cr compound (for both ferromagnetic and antiferromagnetic configurations). In this series, a trend towards an increased anisotropy of the elastic constants, Young modulus Y and Poisson ratio ν is observed. The easy and hard directions of tension can be simply identified by the variation of Y, which corresponds to the presence or absence of covalently bonded–Al–TM–chains. A high anisotropy of the Poisson ratio arises also from an alternation of atoms in the lateral directions and can be understood in the same terms.     

Mineralogy of the clay fraction of soils from the moray cusco archaeological site: a study by energy dispersive X-ray fluorescence, X-ray diffractometry and M?ssbauer spectroscopy

The purpose of this work is to report the advances in the elemental and structural characterization of the clay fraction of soils from the terraces of the Moray Archaeological site, located 38 km north of the city of Cusco, Cusco Region. One sample was collected from each of the twelve terraces of this site and its clay fraction was separated by sedimentation. Previously the pH of the raw samples was measured resulting that all of the samples were from alkaline to strongly alkaline. Energy dispersive X-ray fluorescence (EDXRF) was used for the elemental characterization, and X-ray diffractometry (XRD) and transmission Mössbauer spectroscopy (TMS), using the ?? 14.4 keV nuclear resonance transition in ⁵⁷Fe, were used for the structural characterization of the clays and clay minerals present in each sample. The EDXRF analyses of all the samples show the presence of relatively high concentrations of sulfur in some of the samples and relatively high concentrations of calcium in all of the samples, which may be related to the high alkalinity of the samples. By XRD it is observed the presence of quartz, calcite, gypsum, cronstedtite, 2:1 phyllosilicates, and iron oxides. The mineralogical analysis of Fe by TMS shows that it is present in the form of hematite and occupying Fe^2?+? and Fe^3?+? sites in phyllosilicates, cronstedtite, and other minerals not yet identified.     

Angular momentum limitation of cluster emission from the compound nucleus: 16O(16O, α)28Si and 16O(16O, 8Be)24Mg

Excitation functions of the (¹⁶O, α) and (¹⁶O, ⁸Be) compound reactions on ¹⁶O have been measured and compared with Hauser-Feshbach model calculations. Using transmission coefficients for penetration of the real potential barrier in the exit channels we find global agreement, in contrast to systematic deviations obtained with optical-model transmission coefficients.