Higher order field equations II; Limit properties of green's functions

In a previous paper wave propagation was studied according to a sixth-order partial differential equation involving a complex mass M. The corresponding Yang-Feldman integral equations (indicated as SM-YF-equations), were formulated using modified Green's functions G^M_R(x) and G^M_A(x), which then incorporate the partial differential equation together with certain boundary conditions. In this paper certain limit properties of these modified Green's functions are derived: (a) It is shown that for |M| → ∞ the Green's functions G^M_R(x) and G^M_A(x) approach the Green's functions Δ_R(x) and Δ_A(x) of the corresponding KG-equation (Klein-Gordon equation). (b) It is further shown that the asymptotic behaviour of G^M_A(x) and G^M_A(x) is the same as of Δ_R(x) and Δ_A(x) - and also the same as for D_R(x) and D_A(x) for t→ ± ∞, where D_R and D_A are the Green n's functions for the KG-equation with mass zero. It is essential to take limits in the sense of distribution theory in both cases (a) and (b). The property (b) indicates that the wave propagation properties of the SM-YF-equations, the KG-equation with finite mass and the KG-equation with mass zero are closely related in an asymptotic sense.     

Spectroscopic investigations and luminescence spectra of Nd and Dy doped different phosphate glasses

Spectral properties of Nd³⁺ and Dy³⁺ ions in different phosphate glasses were studied and several spectroscopic parameters were reported. Covalency of rare-earth-oxygen bond was studied in these phosphate glass matrices with the variation of modifier in host glass matrix. Using Judd-Ofelt intensity parameters (Ω₂, Ω₄ and Ω₆), radiative transition probabilities (A) and radiative lifetimes (τ_R) of certain excited states of Nd³⁺ and Dy³⁺ ions are estimated in these glass matrices. From the magnitudes of branching ratios (β_R) and integrated absorption cross-sections (Σ), certain transitions of both the ions are identified for laser excitation. From the emission spectra, peak stimulated emission cross-sections (σ_P) are evaluated for the emission transitions observed in all these phosphate glass matrices for both Nd³⁺ and Dy³⁺ ions.     

A kinetic study of the thermal decomposition process of potassium metabisulfite: Estimation of distributed reactivity model

The thermal decomposition kinetics of potassium metabisulfite was studied by thermogravimetric (TG) and differential thermogravimetric (DTG) techniques using non-isothermal experiments. The apparent activation energy (E_a) is determined using the differential (Friedman) isoconversional method. The results of the Friedman's isoconversional analysis of the TG data suggests that the investigated decomposition process follows a single-step reaction and the observed apparent activation energy was determined as 122.4±2.1 kJ mol⁻¹. A kinetic rate equation was derived for the decomposition process of potassium metabisulfite with contracting area model, f(α)=2(1−α)^1/2, which is established using the Malek's kinetic procedure. The value of pre-exponential factor (A) is also evaluated and was found to be A=1.37×10¹² min⁻¹. By applying the Miura's procedure the distributed reactivity model (DRM) for investigated decomposition process was established. From the dependence α versus E_a, the experimental distribution curve of apparent activation energies, f(E_a), was estimated. By applying the non-linear least-squares analysis, it was found that the Gaussian distribution model (with distribution parameters E₀=121.3 kJ mol⁻¹ and σ=1.5 kJ mol⁻¹) represents the best reactivity model for describing the investigated process. Using the Miura's method, the A values were estimated at five different heating rates and the average A values are plotted against E_a. The linear relationship between the A and E_a values was established (compensation effect). Also, it was concluded that the E_a values calculated by the Friedman's method and estimated distribution curve, f(E_a), are correct even in the case when the investigated decomposition process occurs through the single-step reaction mechanism.     

A new method to determine the electroweak couplings of individual light flavours at LEP

A method is presented for determining the yields and properties of individual light quark flavours in Z ⁰ decays that is essentially free of detailed assumptions about hadronisation. The method uses an equation system with the number of events which are single and double tagged by high energy hadrons as inputs. In addition, SU(2) isospin symmetry and the flavour independence of QCD are used to derive general relations between hadron production from the various primary light quarks. Assuming the branching fractions R _q of the Z ⁰ into down and strange quarks to be the same, five million hadronic Z ⁰ decays may allow precisions of δ(R _d = R _s)/(R _d = R _s) ～ 0.05 and δA _FB(d = s) ～ δA _fb(u) ～ 0.015 for the corresponding asymmetries. The method can be extended to include somewhat more model dependent symmetries of hadron production, which then allows the electroweak observables for each of the individual light quarks to be determined.     

Vibronic-spin-orbit coupling in octachlorodibenzo-p-dioxin

The dipole moments of vibronic transitions P _0R caused by vibronic-spin-orbit coupling along the coordinates of out-of-plane vibration modes R (to which the most intense vibronic lines of the fine-structure phosphorescence spectrum correspond) were calculated for the ³ B _1u (π π*) → S ₀ electronic transition in an octachlorodibenzo-p-dioxin molecule. The dependence of distribution (P _0R )² over R on the constant of spin-orbit coupling ?_A in different atomic groups (A = C, O, α-Cl, and β-Cl) of the molecule is ascertained. The contribution of these atomic groups (related to ?_A) to the value of P _0R ⁱ for the transitions from various triplet i-sublevels of the electronic state is determined. The obtained results about the different effect of the α-Cl and β-Cl atoms on the vibronic P _0R ⁱ and pure electronic transition dipole moments are discussed in connection with experimental data on the weak influence of the amount of chlorine atoms in polychlorinated dioxins on the phosphorescence decay time.     

Theg R -factor of rare-earth nuclei in the Geometric Collective Model

A parameter-free expression for the collective magnetic dipole operator ofee-nuclei is derived within the Geometric Collective Model. Using this result we give an analytical formula for the (g _R ?Z/A)-value of the lower spin groundstate band members foree-nuclei. The general procedure is explained discussing the results (energies, B(E2)-values and quadrupole moments) for^166–170Er-isotopes extensively. The groundstate bandg _R -factors of the isotopes^166–170Er,^153–160Gd,^160–164Dy,^170–174Yb are calculated and compared with experimental data and results of other models.     

MRI magic-angle effect in femorotibial cartilages of the red kangaroo

ObjectiveKangaroo knee cartilages are robust tissues that can support knee flexion and endure high levels of compressive stress. This study aimed to develop a detailed understanding of the collagen architecture in kangaroo knee cartilages and thus obtain insights into the biophysical basis of their function.DesignCylindrical/square plugs from femoral and tibial hyaline cartilage and tibial fibrocartilage were excised from the knees of three adult red kangaroos. Multi-slice, multi-echo MR images were acquired at the sample orientations 0° and 55° (“magic angle”) with respect to the static magnetic field. Maps of the transverse relaxation rate constant (R₂) and depth profiles of R₂ and its anisotropic component (R₂^A) were constructed from the data.ResultsThe R₂^A profiles confirmed the classic three-zone organisation of all cartilage samples. Femoral hyaline cartilage possessed a well-developed, thick superficial zone. Tibial hyaline cartilage possessed a very thick radial zone (80% relative thickness) that exhibited large R₂^A values consistent with highly ordered collagen. The R₂^A profile of tibial fibrocartilage exhibited a unique region near the bone (bottom 5–10%) consistent with elevated proteoglycan content (“attachment sub-zone”).ConclusionsOur observations suggest that the well-developed superficial zone of femoral hyaline cartilage is suitable for supporting knee flexion; the thick and well-aligned radial zone of tibial hyaline cartilage is adapted to endure high compressive stress; while the innermost part of the radial zone of tibial fibrocartilage may facilitate anchoring of the collagen fibres to withstand high shear deformation. These findings may inspire new designs for cartilage tissue engineering.     

The pair distributions and the osmotic coefficient in anomalous electrolytes up to concentrations c≈ 1 mol/1

The osmotic coefficient of anomalous electrolytes up to concentrations c ≈ 1 mol/l is explained by the pair distributions $\text{n(r) =}\text{exp}\text{[-β(}\text{V}{}_{\mathrm{c}}\text{(r) + V(}{}^{\mathrm{hs}}\text{)(r) + V}{}_1\text{(r))]}$. Here $\text{V}$_c(r) is a screened Coulomb potential, V(^hs)(r) a hard sphere potential and V₁(r) = ?A/r⁶ a short range attractive potential. For the contact distances R₊₊, R_?? and R_+? of the hard sphere potentials between ions with the same sign of their charges (++,??) and ions of opposite charges (+?) the relations R₊₊ = R_?? = R and R_+? = q₁R with 0 < q₁ < 1 are assumed. In contrast to a previous paper the parameter q₁ takes a fixed value q₁ ≈ 0,8. The constant A is determined by the fraction q₂ defined by A/R⁶ = q₂(Z²e²/DR) where the positive integer Z is the charge number of the ions and D the dielectric constant of the solvent. The numerical calculation of the osmotic coefficient of 1-1-valent hydrous electrolytes in the range of temperature 273 K ? T ? 293 K shows that the anomalous electrolytes are described by fractions q₂ in the range 0,25 ? q₂ ? 0,5 if the contact distances R are in the range $\text{3}\text{A}\text{?}\text{? R ? 7}\text{A}\text{?}$.     

On the separation of initial and final state effects in photoelectron spectroscopy using an extension of the auger-parameter concept

First, we show that the quantity Δβ(i) = ΔE_A(kii) + 2ΔE_B(i) — ΔE_B(k) is directly related to the final state relaxation contribution ΔE_R(i) of the binding energy shift ΔE_B(i). ΔE_A(kii) is the kinetic energy shift of the Auger transition which corresponds to the decay of a hole state with a hole in level k into a final state with two holes in level i. The shift parameter Δβ(i), which is based on information on two binding energies, is conceptually similar to Wagner's Auger parameter. To establish the relation between Δβ(i) and ΔR(i) one needs, however, less drastic approximations than in the case of Auger parameter shifts. The only approximation necessary is the assumption that ΔR(i) is determined by coulomb contributions.Secondly, we use Δβ (i) to analyse the experimental data of eighteen gaseous phosphorus-containing compounds obtained by Sodhi and Cavell¹. It is shown that ΔR(P_2p) is strongly related to changes in the polarizability of the ligands. The initial state effects derived from our study deviate from those expected on the basis of simple electronegativity considerations.     

Effective biaxial modulus and strain energy density of ideally (h k l)-fiber-textured cubic polycrystalline films

The effective biaxial modulus (M_eff) and strain energy density (W) of cubic polycrystalline films with ideally (h k l) fiber textures are estimated using Vook-Witt (VW) grain interaction model and the data are compared with those derived from Voigt, Reuss and Voigt-Reuss-Hill (VRH) models. Numerical results show that the VW average of M_eff for ideally (1 0 0)- or (1 1 1)-fiber-textured films is identical to the VRH average of M_eff. For (1 1 0) and (1 1 2) planes, however, the VW average of M_eff for (1 1 0)-fiber-textured film is larger than that of (1 1 2)-fiber-textured film when the Zener anisotropic factor (A_R) is not equal to 1. Furthermore, M_eff and W exhibit incremental tendencies with the increase of the orientation factor (Γ_h k l) for the [h k l] axis when A_R > 1, implying that M_eff and W have the minimums on the (1 0 0) plane. Reversely, M_eff and W decrease with the increasing Γ_h k l when A_R < 1. This means that M_eff and W on (1 1 1) plane have the minimums.     

Spectroscopic and optical properties of Nd doped fluorine containing alkali and alkaline earth zinc-aluminophosphate optical glasses

Nd³⁺ doped fluorine containing zinc-aluminophosphate glasses have been prepared with alkali and alkaline earth content to understand the effect of network modifiers on radiative process. The physical and optical properties of these glasses have been evaluated. The Judd-Ofelt model for the intensity analysis of induced electric dipole transitions has been applied to the measured oscillator strengths of the absorption bands to determine the three phenomenological intensity parameters Ω₂, Ω₄ and Ω₆ for each glass. Using these parameters, transition probability (A), total transition probability (A_T), branching ratios (β_R) radiative life times (τ_R) and integrated cross-section (σ_a) for the stimulated emission have been theoretically calculated for certain excited Nd³⁺ fluorescent levels. From the obtained results the conclusion is made about the possibility of using these glasses as laser material.     

Elastic scattering of 56 MeV polarized deuterons on 4He

The differential cross section and the vector and tensor analyzing powers A_y, A_xx, A_yy and A_xz were measured for the d-⁴He elastic scattering at 56 MeV. The measurement of A_xz was performed using a deuteron beam polarized in the horizontal plane. An optical-model analysis of the experimental data was carried out. The magnitude of the tensor analyzing powers could not be reproduced without the tensor potential. By including the T_R type tensor potential, the optical-model calculations give a reasonable reproduction of the experimental data at θ_c.m. < 120°. The obtained T_R tensor potential was much stronger than that predicted by the folding model. The strength of the real T_R potential was roughly in accordance with that obtained from the optical-model analysis of d-⁴He elastic scattering at 20.2 MeV.     

Absorption and emission properties of Nd in lithium cesium mixed alkali borate glasses

Lithium cesium mixed alkali borate glasses of the composition 67B₂O₃·xLi₂O·(32−x)Cs₂O (where x=8, 12, 16, 20 and 24) containing 1 mol% Nd₂O₃ were prepared by melt quenching. The absorption spectra of Nd³⁺ were studied from the experimental oscillator strengths and the Judd-Ofelt intensity parameters were obtained. The intensity parameters are used to determine the radiative decay rates (emission probabilities of transitions) (A_T), branching ratios (β) and integrated absorption cross-sections (Σ) of the Nd³⁺ transitions from the excited state J manifolds to the lower lying J′ manifolds. Radiative lifetimes (τ_R) are estimated for certain excited states of Nd³⁺ in these mixed alkali borate glasses. Luminescence spectra were measured and the emission cross-sections (σ_p) were evaluated for the three emission transitions. The variation of luminescence intensity with x was recorded for the three transitions at different excitation power to see the effect of mixed alkalies in these borate glasses.     

Analysis of the 2ν3 band of 12CD3F at 5.06 μm recorded under high resolution

The 2ν₃(A₁) band of ¹²CD₃F near 5.06 μm has been recorded with a resolution of 20–24 × 10^?3 cm^?1. The value of the parameter (α^B ? α^A) for this band was found to be very small and, therefore, the K structure of the R(J) and P(J) manifolds was unresolved for J < 15 and only partially resolved for larger J values. The band was analyzed using standard techniques and values for the following constants determined: ν₀ = 1977.178(3) cm^?1, B″ = 0.68216(9) cm^?1, D″_J = 1.10(30) × 10^?6 cm^?1, α^B = (B″ ? B′) = 3.086(7) × 10^?3 cm^?1, and β^J = (D″_J ? D′_J) = ?3.24(11) × 10^?7 cm^?1. A value of α^A = (A″ ? A′) = 2.90(5) × 10^?3 cm^?1 has been obtained through band contour simulations of the R(J) and P(J) multiplets.     

Electronic transition-moment variation in the B 2ϵ+−X 2Пr system of the AsO molecule

The spectrum of AsO was excited in a quartz discharge tube and the relative band intensities were measured by using photographic photometry. It was found that the electronic transition moment varies as R_e(r) = constant x (1–0.575r) in the range $\text{1.46}\text{A}\text{?}\text{< r < 1.66}\text{A}\text{?}$. Smoothed relative band strengths are derived for the 11 bands.     

The deformation and orientation effect on reaction cross section with deformed targets

The reaction cross section (σ_R) for a deformed target nucleus and spherical projectile is calculated using the optical-limit approximation of the Glauber-Sitenko theory. A method is presented to include both the density-dependent NN interaction and the higher order deformations of the target nucleus in the collision process. We studied both the orientation and the deformation dependence of σ_R within the energy range 30–900 MeV/A. We found that the orientation of the heavy target nucleus (A ≥ 120) can produce a difference in the calculated σ_R up to 30%. The averaged σ_R over all directions of the symmetry axis of the deformed nucleus differs by less than 1% compared with σ_R calculated for a spherical target with the same rms matter radius as the deformed nucleus. For certain orientation, it was found that σ_R is highly dependent on the hexadecapole deformation. The orientation-averaged cross sections show almost no variation with either the sign or the value of the hexadecapole deformation. We compared the average cross section with the experimental data for several mass numbers; fair agreement is obtained.     

On the stability of the A 15 structure

The pair potential model is applied to problems of thermodynamic stability involving the A 15 structure. Many such problems have been clarified and answered by this procedure. Among the problems considered are the stability of A 15V₃Al and Nb₃Si; the stability of Nb₃(M₁, M₂) and V₃(M₁, M₂) A 15 pseudobinary stability of stoichiometric A15 phases; long range order of A 15 phases; the effect of pressure on the stability of the A 15 structure; the type of phase diagram that is stable in the vicinity of the A 15 phase.     

Total cross sections for 4,6He + 28Si reactions measured at 10–28 MeV/A

New results on the energy dependence of the total cross section (σ _R) for ⁶He scattering on ²⁸Si in the incident energy range 10–28 MeV/A are obtained. The α-particle-production cross sections for the ²⁸Si(⁶He, ⁴He)X channel are measured as well. The secondary beam of ⁶He with an intensity of up to 5×10⁴ particle/s was generated by bombarding a thick beryllium target with ～32-MeV/A ⁷Li ions. In the energy region below 17 MeV/A, σ _R increases sharply. The experimental dependences of the total cross sections are compared with the results of σ _R calculations using the double-folding potential within the optical model. The energy dependence of σ _R for ⁶He differs from that for the neighboring nuclei, which can be associated with the structural features of the former nucleus. The energy spectra of α particles produced in the ⁶He interactions with silicon indicate two mechanisms of their production: transfer reaction and ⁶He breakup in the field of the ²⁸Si nucleus.     

Optical and thermal properties of F and F aggregate centers in KF

A detailed investigation has been carried out of the optical and thermal properties of centers such as F, F_A, M and M_A in pure, Na-doped and Li-doped KF. Most centers exhibit properties which are qualitatively similar to those produced in other potassium halides with the notable exception of the F_A (Na) center, which has both Type I and Type II behavior.