Rb蒸气中的5PJ+5PJ′→5S+5DJ″碰撞能量合并

研究了Rb(5PJ) Rb(5PJ′)→Rb(5S) Rb(5DJ″)的碰撞能量合并过程,一台单模半导体激光器共振激发Rb原子的5P1/2或5P3/2态,另一与泵浦激光束反向平行的单模激光束作为吸收线探测激发态原子密度及其空间分布,吸收线分别调至5P1/2→5D3/2和5P3/2→7S1/2跃迁,由激发态原子密度和谱线荧光比得到碰撞能量合并过程5PJ 5PJ′→5S 5DJ″的截面.两台激光器同时分别激发5P1/2和5P3/2态,通过对5DJ″→5PJ的荧光探测,得到5P3/2 5P1/2碰撞转移到5D5/2和5D3/2的截面分别为(1.12±0.50)×10-14和(1.01±0.45)×10-14cm2.     

On the kinetics of the C5H5 + C5H5 reaction

The possibility that the reaction between two cyclopentadienyl radicals (cC₅H₅) may lead to the production of naphthalene has been the subject of considerable theoretical and experimental studies. Though it has been proposed that this reaction may be the main channel for the formation of naphthalene in many combustion environments, the elementary mechanism leading from the initial adduct (C₅H₅_C₅H₅) to naphthalene is still not clear. In this study the portion of the C₁₀H₁₀ PES accessible to C₅H₅_C₅H₅ has been theoretically re-examined using density functional theory to locate stationary points and the CBS-QB3 computational protocol to determine energies. A new reaction pathway leading to the formation of a set of azulyl radicals was identified. Since it is known that azulyl radicals can easily decompose to naphthalene and atomic H, the proposed pathway provides an effective route for the formation of naphthalene. Channel specific kinetic constants were determined between 1100 K and 2000 K integrating the master equation for a PES comprising both this reaction pathway and the literature reaction pathway, which main product is the fulvalenyl radical. It was found that the main reaction channel is decomposition to reactants in the whole temperature range investigated and that the azulyl reaction channel is dominant over the fulvalenyl pathway up to 1450 K. The rate constants calculated at 1 bar for the azulyl and fulvalenyl reaction channels are 10^14.72T(K)^?0.853 exp(?3650/T(K)) and 10^10.30T(K)^0.951 exp(?7948/T(K)) cm³/mol/s, respectively. The rate constant for the formation of naphthalene through the azulyl channel is consistent with recent estimates based on the kinetic simulation of the pyrolysis and oxidation of cyclopentadiene.     

Facteurs de lande des niveaux des configurations 5s5p et 5s5d de cd I

A plane Fabry-Pérot is used to measure, with a precision of about 10^-4, the Landé factor of the levels issued from the 5s5p and 5s5d configurations of cadmium I. Calculations taking into account intermediate coupling effects and the anomalous gyromagnetic ratio of the free electron are insufficient to explain some experimental data; in such cases it is necessary to perform a more detailed analysis of the corrections due to the relativistic effects.     

Ti5O5 superstructures of cubic titanium monoxide

A cubic model is proposed for the Ti₅O₅ (Ti₅?O₅□ ≡ Ti₉₀?₁₈O₉₀□₁₈) superstructure of nonstoichiometric titanium monoxide Ti _x O _z with double imperfection. The unit cell of the cubic Ti₅O₅ superstructure has the threefold lattice parameter of the unit cell of the basis disordered B1 structure of Ti _x O _z monoxide and belongs to space group $Pm\bar 3m$ . The channel of the disorder-order transition, i.e., Ti _x O _z (space group $Fm\bar 3m$ )-Ti₅O₅ (space group $Pm\bar 3m$ ), includes 75 superstructure vectors of seven stars {k ₁₀}, {k ₇}, {k ₆₍₁₎}, {k ₆₍₂₎}, {k ₄₍₁₎}, {k ₄₍₂₎}, and {k ₁}. The distribution functions of Ti and O atoms over the sites of the cubic Ti₅O₅ superstructure are calculated. A comparison of the X-ray and electron diffraction data obtained for ordered TiO_1.087 monoxide with the theoretical simulation results supports the existence of the cubic Ti₅O₅ superstructure. The cubic (space group $Pm\bar 3m$ ) Ti₅O₅ superstructure is shown to be a high-temperature structure relative to the well-known monoclinic (space group C2/m) superstructure of the same type.     

Two-Brane Randall-Sundrum Model in AdS 5 and dS 5

Two flat Randall-Sundrum three-branes are analyzed, at fixed mutual distance, in the case where each brane contains an ideal isotropic fluid. Both fluids are to begin with assumed to obey the equation of state p = ( – 1), where is a constant. Thereafter, we impose the condition that there is zero energy flux from the branes into the bulk, and assume that the tension on either brane is zero. It then follows that constant values of the fluid energies at the branes are obtained only if the value of is equal to zero (i.e., a vacuum fluid). The fluids on the branes are related: if one brane is a dS ₄ brane (the effective four-dimensional constant being positive), then the other brane is dS ₄ also, and if the fluid energy density on one brane is positive, the energy density on the other brane is larger in magnitude but negative. This is a non-acceptable result, which sheds some light on how far it is possible to give a physical interpretation of the two-brane scenario. Also, we discuss the graviton localization problem in the two-brane setting, generalizing prior works.     

Thermomagnetic history effects in LaCo5xNi5−5x and ThCo5xNi5−5x compounds

The magnetization versus temperature curves of several compounds of the series LaCo_5xNi_5?5x were found to give rise to an abrupt increase at temperatures being higher in accordance as the applied field strengths are smaller. The magnetic properties strongly depend on the magnetic as well as on the thermal history. The observed magnetic behaviour is discussed in terms of mictomagnetism and narrow Block wall propagation.     

Corrosion of 85-5-5-5 bronze in natural and synthetic acid rain

In order to investigate the decay of bronzes exposed to acid wet depositions, a comparative study has been performed by following the corrosion behaviour of different sets of bronze specimens exposed either to natural rain or to a similar solution, without organic compounds, artificially reproduced in laboratory. The as cast G85 bronze specimens were exposed to aggressive solutions for different periods through a wet-dry technique. The pH trend of the solutions and the amount of metals transferred into the solutions were periodically monitored. OM, SEM, XRD, RAMAN analyses and ac electrochemical measurements were performed on the artificially weathered specimens. Preliminary results, showing the difference between the ageing in natural and synthetic rain, suggest the influence of the organic components on the corrosion process. In particular, the growth of a more uniform protective layer of corrosion products on the metal surface exposed to the natural rain could be attributed to these components. PACS 82.45.Bb; 82.33.Tb     

Theoretical study of structures of Ga5N5 cluster

The structures and energies of a Ga₅N₅ cluster have been calculated using a full-potential linear-muffin-tin-orbital (FP-LMTO) method, combined with molecular dynamics technique. Twenty-four structures for a Ga₅N₅ cluster have been obtained. The most stable structure is a C₁ planar structure with a N₃ subunit. The Ga₅N₅ clusters show a preference for a N₃ subunit, revealing the same behavior as in the Ga₃N₃ and Ga₄N₄ clusters. The existence of strong N–N bonds dominates the structure of a Ga₅N₅ cluster. Through the calculation of the density of states we found that the most stable structure of Ga₅N₅ clusters presented semiconductor-like properties.     

Dynamics of cyclohexadienyl radicals in NaZSM-5 and LiZSM-5

The dynamics of the muonium substituted cyclohexadienyl radical adsorbed on NaZSM-5 and LiZSM-5 was investigated. Avoided-level-crossing muon spin resonance studies revealed extensive surface-sorbate interactions and showed a strong effect of the nature of the metal dopants on the radical mobility.     

Optische übergangswahrscheinlichkeiten der Konfigurationen 3p 5 4s–3p 5 5p des Argon I

Optical transition probabilities of the configurations 3p ⁵ 4s–3p ⁵ 5p of Argon I were determined in a wall-stabilized arc plasma and compared with the theoretical results for different types of spin-orbit-coupling. Mostly the differences in the results forLS-jl- and intermediate-coupling are small compared with the deviations of the experimental values. Therefore it may be presumed that in some cases not the assumption of an approximately valid coupling scheme is responsible for the errors of the theoretical transition probabilities, but the other quantum mechanical approximation processes.     

Hodge Dual Symmetry of Green-Schwarz Superstring in AdS5 S^5

The hidden symmetry and an infinite set non-local conserved currents of the Green-Schwarz superstring on AdS549 S^5 have been pointed out by Bena et al. In this paper, we show that the Hodge dual between the Maurer Caftan equation and the equation of motion gives the hidden symmetry in the moduli space of Green-Schwarz superstring. Thus by twisty transforming the vielbeins, we can express the currents of the paper [I. Bena, J. Polchinski, and R. Roiban, Phys. Rev. D 69 （2004） 0460021 as the Lax connections bv a uniaue spectral narameter.     

Eu3+掺杂5Li2O-1Nb2O5-5TiO2发光陶瓷的制备及性能研究

以Li2CO3、Nb2O5、TiO2和Eu2O3为原料,采用固相法制备Eu3+掺杂的5Li2CO3-1Nb2O5-5TiO2(LNT)发光介质陶瓷.通过密度、XRD和荧光光谱测试,对0.2%(质量分数)Eu2O3掺杂的陶瓷片进行性能表征.结果表明:1 120 ℃烧结致密的陶瓷片,其晶相结构为"M-相"与Li2TiO3两相复合构成;在400 nm的近紫外光激发下,样品有较强的橙光(592 nm)和红光(615 nm)发射,分别属于Eu3+的5D0→7F1的磁偶极跃迁和5D0→7F2的电偶极跃迁.     

Fluorescence Emitted During the Autooxidation of 2,3,4,6-tetrahydroxy-5H-benzocyclohepten-5-one

Data suggest that the purpurogallin (2,3,4,6-tetrahydroxy-5H-benzocyclohepten-5-one, hydroxybenzotropolone) and its analogues formed from the polyphenols can be precursors of the most complex natural compounds—humic acids and melanin-like polymers. Therefore, to confirm this possibility, the autooxidation of purpurogallin to humus-like substances has been performed. The oxidation process has been assayed by means of fluorescence and UV/VIS absorption spectroscopy. The obtained results indicate that purpurogallin undergoes a free-radical-mediated autooxidation via purpurogallinquinones to humus-like polymers. The scheme of the complex transformation of purpurogallin has been proposed.