Stochastic model of angular distributions of fragments originating from the fission of excited compound nuclei

The anisotropy of angular distributions of fission fragments and the average multiplicity of prescission neutrons were calculated within a stochastic approach to fission dynamics on the basis of three-dimensional Langevin equations. This approach was combined with a Monte Carlo algorithm for the degree of freedom K (projection of the total angular momentum I onto the fission axis). The relaxation time τ _K in the coordinate K was considered as a free parameter of the model; it was estimated on the basis of a fit to experimental data on the anisotropy of angular distributions. Specifically, the relaxation time τ _K was estimated at 2 × 10^?21 s for the compound nuclei ²²⁴Th and ²²⁵Pa and at 4 × 10^?21 s for the heavier nuclei ²⁴⁸Cf, ²⁵⁴Fm, and ²⁶⁴Rf. The potential energy was calculated on the basis of the liquid-drop model with allowance for finiteness of the range of nuclear forces and for the diffuseness of the nuclear surface. A modified one-body viscosity mechanism featuring a coefficient k _s that takes into account the reduction of the contribution from the wall formula was used to describe collective-energy dissipation. The coefficient k _s was also treated as a free parameter and was estimated at 0.5 on the basis of a fit to experimental data on the average prescission multiplicity of neutrons.     

Nucleon-content effect on the fission lifetime of excited nuclei

It was shown previously that the fission lifetime of a nucleus excited to about 100 MeV depends strongly and nonmonotonically on the initial value of its angular momentum L ₀. This result was obtained on the basis of a refined version of the combined dynamical and statistical model. The present study is devoted to a theoretical analysis of the dependence of the fission time on the nucleonic composition of the nucleus involved. The respective calculations were performed within the same model. The dependence of the average fission time 〈t _f 〉 on the initial fissility parameter (Z ²/A)₀ appears to be of a resonance type and is similar to its dependence on L ₀. This dependence of the average fission time on (Z ²/A)₀ stems both from statistical calculations and from a dynamical simulation of the fission mode with allowance for friction. The conditions under which the average fission time reaches a maximum are specified. The dependence of the average fission time on (Z ²/A)₀ remains nonmonotonic in the fusion-fission reaction as well, in which case the distribution of compound nuclei with respect to the initial angular momentum is broad.     

Preliminary results of the experiment on search for neutron nuclei on a nuclear reactor

An experiment on search for neutron nuclei in the reaction of neutron-induced fission of ²³⁵U nuclei has been performed on a nuclear reactor. The hypothetical reaction ¹²²Te(^xn, (x ? k)n)^{122 + k} Te → (β^?) → ^{122 + k} I (x = k ≥ 10) has been investigated. The radiochemical method for selecting iodine isotopes from tellurium was used. The upper limit on the probability of formation of neutron clusters has been obtained: P _k ≤ 10^?8 (fission)^?1 for ¹¹n clusters and P _k ≤ 10^?9 (fission)^?1 for ¹¹n clusters.     

Vibronic-spin-orbit interactions in heterocyclic analogues of fluorene with the N and O heteroatoms

The transition dipole moments P _0n ^s for the transitions from the electronic triplet state ³ B ²(ππ*) to vibrational sublevels of the vibrational out-of-plane modes n of the carbazole and dibenzofuran molecules are calculated. The values of the radiative deactivation rate constant k _rad ^s of the triplet sublevels T ^s are determined along with the components k _SO ^s and k _VSO ^s of this constant, which depend on the intramolecular spin-orbit (SO) and vibronic-spin-orbit (VSO) interaction. It is ascertained that k _rad ^z > k _rad ^y . For different structural units of the molecules (the heteroatom and the carbon atoms of the dibenzene fragment), the effect of the SO coupling on the constant k _VSO～Σ_{s, n} (P _0n ^s )² is studied. A competition between the effects on k _VSO from the SO coupling in the carbon atoms and in the light N and O heteroatoms is revealed. This competition accounts for the weak influence of the heteroatom on this component of the rate constant k _rad in these molecules. It is ascertained that the intensity distribution among the vibronic lines in the phosphorescence spectra of carbazole and dibenzofuran I _0n ～Σs (P _0n ^s )² is different due to the substantially different influence of the N and O heteroatoms on the deactivation of the triplet sublevel T ^y .     

Retardation of unimolecular reactions in the solid phase

The retardation coefficient, K _R = k _l/k _s, for a homogeneous reaction in the bulk of a crystal was calculated within the framework of the free-volume model of unimolecular reactions in the solid phase in the approximation of an isotropic continuum. The key parameters entering into the working formula, more specifically, the additional activation volume for the solid phase and the compressibility coefficient, were estimated using semiempirical methods. The calculated values of K _R range from several units to several thousand units, an interval that encompasses all the experimental values of this quantity. Low values of K _R are indicative of reactions in the bulk of the crystal lattice. In addition, reactions on defects can occur, being predominant at K _R > 100. In all cases, the calculated values of K _R give an upper estimate of the degree of retardation, above which no experimental values have been obtained.     

Dasβ-Spektrum des Cs137

Theβ-ray spectrum of Cs¹³⁷ has been measured with an iron-free spectrometer. The energy of the soft component was found to beE ₀=514±2 keV. The parameterk of the hard-component shape factorC _2VA ⁽²⁾ (W)=q ²+kp ² was determined to bek=0.015±0.004. Theβ intensities amount to 6.5% (hard component) and 93.5% (soft component). TheK conversion coefficient of the isomeric transition was measured to beα _K=0.093±0.003, in excellent agreement withSliv's theoretical value.     

Prompt-fission-neutrons spectra of <Superscript>238</Superscript>U

The spectra of prompt fission neutrons from the reaction ²³⁸U(n, F) for neutrons of energy in the range E _n ≤ 20 MeV are interpreted within the statistical model. It is shown that exclusive spectra of prefission neutrons emitted in (n, xnf) reactions play a decisive role in describing the observed promptfission-neutron spectra and determine the average energies of prompt-fission neutrons. The dependence of the effect of prefission neutrons on the fissility of a target nucleus is demonstrated for the reactions ²³²Th(n, F), ²³⁵U(n, F), and ²³⁹Pu(n, F).     

Energy spectra of developed superfluid turbulence

Turbulence spectra in superfluids are modified by the nonlinear energy dissipation caused by the mutual friction between quantized vortices and the normal component of the liquid. We have found a new state of fully developed turbulence, which occurs in some range of two Reynolds parameters characterizing the superfluid flow. This state displays both the Kolmogorov-Obukhov 5/3-scaling law E_k ∝ k^?5/3 and a new “3-scaling law” E_k ∝ k^?3, each in a well-separated range of k.     

Novel features of the fragment mass variance in fission of hot nuclei

On the basis of data obtained by the incomplete fusion reactions ⁷Li(43A MeV)+²³²Th and ¹⁴N(34A MeV)+¹⁹⁷Au, the energy dependence of the variance (σ _M ² ) of the fragment mass in fission of highly heated nuclei has been investigated for total excitation energies E _tot ^* ranging from 50 up to 350 MeV. The dependence σ _M ² E _tot ^* shows some unexpected features when E _tot ^* exceeds a value of about 70 MeV. After this value, the steady increase of σ _M ² expected from its temperature dependence changes to some kind of plateau between 100 and 200 MeV. Further on, at E _tot ^* in excess of about 250 MeV, the variance is found to increase again sharply. In order to analyze this behavior quantitatively, a dynamical stochastic model has been developed. The model employs the one-body dissipation mechanism and describes the decay of highly excited and rotating nuclei by fission and light-particle evaporation. It satisfactorily explains the measured prior-to-scission neutron multiplicities and the experimental mass variances up to E _tot ^* ?250 MeV, but the stochastic treatment does not reveal any increase in σ _M ² at higher excitation energies in contradiction with the data.     

Fluorescence quenching of vaporous polycyclic aromatic hydrocarbons by oxygen

The fluorescence quenching by oxygen of vapors of nine polycyclic aromatic hydrocarbons with strongly different oxidation potentials 0.44 eV < E _ox < 1.61 eV (anthracene, 9-methylanthracene, 2-aminoanthracene, 9,10-dibromanthracene, pyrene, chrysene, phenanthrene, fluoranthene, and carbazole) is studied. From the dependences of the fluorescence decay rates and intensities on the oxygen pressure P _O2, the quenching rate constants k _S ^O2 for the excited singlet states S ₁ and the fraction f _S ^O2 of the S ₁ states quenched by oxygen are estimated. At P _O2 = 5 Torr, the k _S ^O2 constants vary from 1.2 × 10⁷ to 3.0 × 10⁵ s^?1 Torr^?1, while the fraction of the quenched excited singlet states changes from 0.1 (fluoranthene) to 0.7 (chrysene) and 0.8 (pyrene). The dependences of k _S ^O2 on the photophysical and electron-donor characteristics of the fluorescing compounds are analyzed. It is shown that, in the gas phase of anthracene and its derivatives, the magnitudes of k _S ^O2 are limited by the rate constants of gas-kinetic collisions k _gk and do not depend on the electron-donor characteristics of fluorophores, while the fraction of quenched states f _S ^O2 changes with the oxidation potential. For compounds with k _S ^O2 < k gk, both the rate constants k _S ^O2 and the fraction of quenched states f _S ^O2 depend on the E _ox of sensitizers, which demonstrates an important role played by the charge-transfer interactions in quenching of the S ₁ states. The dependence of the rate constants k _S ^O2 on the free energy of electron transfer ΔG _et is considered.     

Reaction dynamics at the barrier for heavy compound systems

To investigate basic properties of the fusion reaction dynamics for heavy compound systems, the partial wave distribution σ _l extracted from measured γ multiplicities can be employed as an alternative to the classically used fusion/fission excitation functions. A variety of reactions leading to compound nuclei in the Pb region can be used to investigate features like the fusion-fission competition, the role of deformation in the fusion of heavy systems, and a possible effect of the Z=82 shell on the enhancement of evaporation residue production. The measured spin distribution can provide information on the single partial wave cross sections, which is hidden in the integral fusion cross section. Moreover, it can reveal signatures in the high-spin region, which could be an indication of a stabilization due to an increase in the potential hole by shell correction energies E_shell in the vicinity of a closed shell. The systematic investigation and understanding of the fusion-fission reaction dynamics, together with the understanding of the structure of transfermium nuclei, which are stabilized only via shell effects, are essential for a successful program aiming at the synthesis of new elements at GSI, Dubna, or elsewhere. We started a series of experiments to measure those properties for the reactions at the Laboratori Nazionali di Legnaro, Italy. In order to extract the compound nucleus spin distribution, γ multiplicities are measured using the γ-detector array GASP and its inner ball in the multiplicity filter mode.     

Aussagen der Theorie von Kraichnan für die isotrope hydromagnetische Turbulenz

The theory ofKraichnan is applied to quasi-stationary isotropic hydromagnetic turbulence. The average infinitesimal-impulse-response functionsg(k, τ), g _m (k, τ) and the time-correlationsr(k, τ), r _m (k, τ) are evaluated by the non-local direct-interaction approximation within the inertial range. For the range of ohmic but no viscous dissipation it is found that the magnetic energy spectrumE _m (k) obeys aE(k)k ^?2-law in accordance with results ofGolitsyn andMoffatt.     

Integral characteristics of vibronic-spin-orbit interactions in a phosphorus-containing analogue of the fluorene molecule

The strengths (P ₀₀ ^s )² and F _VSO ² of the transitions from the triplet sublevels s = z, y, and x of the electronic state ³A″ of the phenyldibenzophosphole (DB(P-Ph)) molecule are calculated taking into account the intramolecular spin-orbit (SO) and joint vibronic-spin-orbit (VSO) interactions. The contributions to the vibronic transition strengths from the SO interactions in different structural elements of the molecule (the C atoms of the dibenzene framework, the P atom, and the Ph substituent) are determined. The effect of the nonplanar nuclear configuration of the DB(P-Ph) molecule on the values of F _VSO ^s is investigated. The radiative deactivation rate constants of the k _rad ^s triplet sublevels T ^s are estimated. It is found that the vibrations of the A′(B₁) symmetry in the fine-structure phosphorescence spectrum of DB(P-Ph) occur due to both the SO coupling exclusively in the P atom and the T ^x → S₀ transition (the x axis is perpendicular to the planar dibenzene framework of the molecule) with a high (preferential) population of this triplet sublevel.     

Randall–Sundrum II model from small field inflation in light of planck data and reheating temperature

We focus on the behaviours of small field of an arctangent potential form, in Randall–Sundrum II braneworld. Within this framework, there is only one brane with positive tension while the second membrane is sent to infinity, and the configuration the model allows to localize the gravity on the curvature of the bulk. In that context, we found that inflationary observables (n _s, r, and dn _s/dlnk) depend only on the e-folding number N. From the power perturbation value P _R (k) given by the latest observational measurements, we evaluate the values of brane tension λ and the energy scale V ₀, and we have shown that the various inflationary perturbation parameters are widely consistent with the recent Planck data for a suitable choice of value of the number N. Concerning the reheating phase, we found a large value of the temperature T _re ～ 5 × 10¹⁴ GeV.     

Unified Mechanism behind the Appearance of <Emphasis Type="Italic">T</Emphasis>-Odd TRI and ROT Asymmetries in Actinide Fission Induced by Cold Polarized Neutrons

Some shortcomings of the approaches that are used to describe T-odd ROT and TRI asymmetries in true ternary fission via reactions involving the emission of prescission alpha particles and which are based on employing the classical method of trajectory calculations are analyzed. These shortcomings are caused by the disregard of the interference between the fission widths of different sJ_s neutron resonance states formed in the first well of the deformation potential of fissile compound nuclei. It is shown that the method used in some studies to determine T-odd TRI-asymmetries for prescission alpha particles is at odds with basic concepts of the generalizedmodel of the nucleus and approaches to constructing collective (for example, bending) vibrations of a fissile compound nucleus. Quantum-mechanical fission theory is generalized via employing a unified mechanism of formation of T-odd TRI and ROT asymmetries for prescission alpha particles and evaporated photons (neutrons). The proposed mechanism takes correctly into account the effect of quantum rotation of a fissile compound nucleus on the angular distributions of fission fragments and alpha particles for true ternary fission, as well as on the angular distribution of prompt photons (neutrons) emitted by fragments originating from the delayed fission of the aforementioned nuclei.     

Scattering the Geometry of Weighted Graphs

Given two weighted graphs (X, b_k, m_k), k =?1,2 with b₁ ～ b₂ and m₁ ～ m₂, we prove a weighted L¹-criterion for the existence and completeness of the wave operators W_±(H₂, H₁, I_1,2), where H_k denotes the natural Laplacian in ?²(X, m_k) w.r.t. (X, b_k, m_k) and I_1,2 the trivial identification of ?²(X, m₁) with ?²(X, m₂). In particular, this entails a general criterion for the absolutely continuous spectra of H₁ and H₂ to be equal.     

Effect of vibronically induced spin-orbit coupling of electronic ππ* states on nonradiative intersystem crossing: Naphthalene

The effect of (I) S ₁(¹ B _2u ) ? T ₁(³ B _1u ) and (II) S ₁ ? T ₂ (³ B _3g ) ? T ₁ transitions in naphthalene on the rate constant K _ST ^s of the S ₁ ? T ₁ nonradiative transitions to all triplet sublevels s = z, y, x of the T ₁ state has been investigated in the approximation of vibronically induced spin-orbit couplings, taking into account all out-of-plane vibrational modes. The shapes of the vibrational modes that are most active in these transitions are determined. The calculated values K _ST = (0.33–0.75) × 10⁷ s^?1, obtained with allowance for the I and I + II transitions, are consistent with the experimental values (K _ST)_exp found by different researchers. It is established in all calculation versions that K _ST > K _ST ^z > k _ST ^x . This relation is in qualitative agreement with the known magnetooptical data.     

Oxidation of the aniline–styrene epoxide-<Emphasis Type="Italic">p</Emphasis>-toluenesulfonic acid ternary system in polar solvents: Trends and mechanism

Investigation of the kinetics of oxygen absorption by the aniline–styrene epoxide-p-toluenesulfonic acid ternary system (TS) in an acetonitrile solution led to a simple equation for the oxidation rate: V _TS = k[aniline]⁰ ? [epoxide]⁰[acid]¹ at [aniline], [epoxide] ? [acid], k = 0.77 × 10^–3s^–1, and 343 K. The data obtained indicated that a complex of the three starting reagents formed before oxidation. In a mixed solvent containing tert-butanol, the dependence of V _TS on its composition was extremum. A scheme was suggested that explained the change in the dependence V _TS = k′[aniline]^–0.63[epoxide]^0.86[acid]¹ in the mixed solvent by the decomposition of the complex in the presence of alcohol.