Rotational Analysis of the B2Σ+-X2Σ+ Bands of 12C18O+

The emission spectrum of the B²Σ⁺-X²Σ⁺ (First Negative) system of the molecular ion ¹²C¹⁸O⁺ have been photographed at a resolution sufficient to observe the spin splitting of the lines with N > 18. Four bands, 0-1, 0-3, 1-4 and 2-5, have been rotationally analyzed and the molecular constants of the B²Σ⁺ , v = 0,1, 2 and X²Σ⁺ , v =1, 3, 4, 5 have been obtained.     

Isotopic Effects on Stereodynamics of the C~+ + H_2→CH~+ + H Reaction

The effects of isotope substitution on stereodynamic properties for the reactions C~+ + H_2/HD/HT →CH~+ + H/D/T have been studied applying a quasi classical trajectory method occurring on the new ground state CH_2~+ potential energy surface [J. Chem. Phys. 142(2015) 124302]. In the center of mass coordinates applying the quasi classical trajectory method to investigate the orientation and the alignment of the product molecule. Differential cross section and three angle distribution functions P(θ_r), P(ф_r), P(θ_r, ф_r) on the potential energy surface that fixed the collision energy with a value is 40 kcal/mol have been studied. The isotope effect becomes more and more important with the reagent molecules H_2 changing into HD and HT. P(θ_r, ф_r) as the joint probability density function of both polar angles θ_r and ф_r, which can illustrate more detailed dynamics information. The isotope effect is obvious influence on the properties of stereodynamics in the reactions of C~+ + H_2/HD/HT → CH~+ + H/D/T.     

Effect of violating t-invariance of the electromagnetic interaction of hadrons in the processes n + p → d + γ and n + → d + e++e−

T-odd correlations that are possible in the processes n + p d + and n + p d + e⁺ + e^e- and that arise due to the capture of thermal neutrons are determined in terms of threshold amplitudes (for the process n + p d + @#@) or electromagnetic inelastic form factors (for the process n + p d+ e⁺ + e^e§-). The mechanism of these reactions is not given in concrete form, but those general properties of the electromagnetic hadronic current are used that are preserved with three-dimensional reflections.Translated from Izvestiya Vysshikh Uchebnykh Zavedenii, Fizika, No. 10, pp. 8–13, October, 1986.     

Rotational Analysis of the 1–4 Band of the B 2Σ+–X 2Σ+ System of 14C16O+

ABSTRACT

High-resolution emission spectrum of the 1–4 band of the B ²Σ⁺–X ²Σ⁺ transition of ¹⁴C¹⁶O⁺ was observed for the first time by conventional emission spectroscopy. The band spectrum was excited in a water-cooled Geissler lamp filled with commercial gaseous carbon monoxide enriched in about 80% of the radiocarbon ¹⁴C. A rotational analysis has been carried out and obtained molecular constants have been merged with previously published data for the B ²Σ⁺–A ²Π_i and A ²Π_i–X ²Σ⁺ transitions. The principal equilibrium constants for the ground X ²Σ⁺ state obtained from this work are ω_e = 2121.7726(98), ω_e x _e = 13.9055(27), B _e = 1.815290(30), α_e = 1.6594(33) × 10^?2, and γ_e = ? 0.377(73) × 10^?4 cm^?1. Also, presently known experimental equilibrium molecular constants of the X ²Σ⁺ states of the CO⁺ isotopic molecules are summarized and isotopic dependence of the B _e and ω _e constants is discussed.     

Study of the mechanism of the 3He + p → p + p + d reaction at a 3He momentum of 5 GeV/c

The mechanism of the reaction ³He + p → p + p + d is studied by making use of the ITEP 80 cm liquid-hydrogen bubble chamber exposed to a beam of 5 GeV/c ³He nuclei. The reaction cross section is equal to 20.6 ± 0.3 mb. The phase-space regions associated with quasifree scattering (QFS) and final-state interactions (FSI) are selected. Angular, mass and momentum distributions of the reaction products are obtained in the entire kinematically allowed range. The experimental data in the QFS region are compared with theoretical calculations based on the simplest pole-diagram approximation. The ³He and deuteron wave functions (WF) correspond to the realistic RSC potential. The D-wave components of these WF are taken into account. The absolute value of the cross section and shape of the distributions are described as a whole reasonably well within the frame of the model considered in the kinematical region where FSI may be neglected. But at large spectator momenta there is an essential disagreement. The possible reasons for this are discussed.     

Influence of reagent vibration on the stereodynamics of the Li + HF → LiF + H reaction

We investigate the influence of reagent vibration on the stereodynamics of the title reaction by the quasi-classical trajectory on the Aguado-Paniagua2-potential energy surface developed by Aguado et al. (J. Chem. Phys. 1997 106 1013). The cross sections and reaction probability as functions of the reagent vibration are calculated in the centre-of-mass frame. The product angular distributions of p(θ_r), p(φ_r), and p(θ_r, φ_r), which reflect the vector correlation, are also presented and discussed. The results indicate that the vector properties are sensitively affected by the vibrational excitation.     

Coherent laser spectroscopy of ¯pHe+

The facilities of the coherent laser pulse spectroscopy of the ¯pHe⁺ transitions are considered taking the magnetic structure of the energy levels into account. The possibility for the observation of the dynamics of intramolecular motions is also analyzed.     

J~P assignments of Λ_c~+ baryons

The "good" diquark is employed to study Λ_c~+ baryons within a mass loaded flux tube model. The study indicates that all Λ_c~+ baryons candidates in the 2008 review by the Particle Data Group (PDG) are well described in the mass loaded flux model. The quantum numbers J~P of these Λ_c~+ candidates are assigned. If Λ_c(2765)~+ is an orbitally excited Λ_c~+, it is likely the J~P=3~+/2 one. If Λ_c(2765)~+ is an orbitally excited Σ_c, there ought to be another J~P = 3~+/2 Λ_c~+ with mass ≈ 2770 MeV. In the model, there exists no J~P = 1~+/2 Λ_c~+ (≈ 2700) predicted in existing literature. Λ_c(2940)~+ is very possible the orbitally excited baryon with J~P = 5~-/2.     

Analysis of the bands of the B2Σ+-X2Σ+ transition in 12C16O+ and 13C16O+

The First Negative bands of ¹²C¹⁶O⁺ and ¹³C¹⁶O⁺, in the spectral region 40 000–46 000 cm⁻¹, have been photographed at a resolution sufficient to resolve the spin-doubled components. These data for ¹²C¹⁶O⁺, along with previously reported data of the same transitions, as well as microwave transitions of ¹²C¹⁶O⁺ in the ground state, have been explicitly included in a least-squares fit to determine the most precise set of molecular constants to date for the B²Σ⁺ and X²Σ⁺ states of ¹²C¹⁶O⁺. Furthermore, we report a rotational analysis of the First Negative bands of ¹³C¹⁶O⁺ for the first time. Several molecular constants characterizing ¹³C¹⁶O⁺ in the B²Σ⁺ and the X²Σ⁺ states, including spin-doubling parameters, have been determined.     

On polarization of strange baryons in reactions p + p↦p + Λ0 + K+ and p + p↦p + Σ0 + K+ near thresholds

Polarization properties of strange baryons produced in pp reactions, p + p↦p + Λ⁰ + K⁺ and p + p↦p + Σ⁰ + K⁺, near thresholds of the final states pΛ⁰K⁺ and pΣ⁰K⁺ are analysed relative to polarizations of colliding protons. The cross-sections for pp reactions are calculated within the effective Lagrangian approach accounting for strong pp rescattering in the initial state of colliding protons with a dominant contribution of the one-pion exchange and strong final-state interaction of daughter hadrons (Eur. Phys. J. A 9, 425 (2000)). Received: 22 October 2001 / Accepted: 14 November 2001     

Quasi-classical trajectory study of the stereodynamics of a Ne+H2+→NeH++H reaction

We have carried out a quasi-classical trajectory calculation for the reaction of Ne + H₂⁺ (v=0, j=1) → NeH⁺ + H on the ground state (1²A') using the LZHH potential energy surface constructed by Lü et al. [Lü S J, Zhang P Y, Han K L and He G Z 2010 J. Chem. Phys. 132 014303]. Differential cross sections at many collision energies indicate that the reaction is dominated by forward-scattering. In addition, the NeH⁺ product shows rotationally hot and vibrationally cold distributions. Stereodynamical results indicate that the products are strongly polarized in the direction perpendicular to the scattering plane and that the products rotate mainly in planes parallel to the scattering plane.     

The effect of humidity on the ionic conductivity of Mg2+-stabilized K+-β-ferrite

The ionic conductivity of Mg²⁺-stabilized potassium β-ferrites was studied in wet and dry air atmosphere and in the temperature range between room temperature and 500 °C. Several conductivity processes were determined. The impedance spectroscopic measurements were combined with thermogravimetric analysis data, and a microscopic interpretation for the effect of humidity on the conductivity of K⁺-β-ferrite is proposed. Between 400 and 500 °C, a change in the conductivity behavior is observed which is associated with the magnetic ordering temperature and a structural ordering in the conductivity planes of the materials. The activation energy values of the different conduction processes have been calculated.     

Laser-induced-fluorescence Fourier transform spectrometry of the XOg+ state of I2: Extensive analysis of the BOu+ → XOg+ fluorescence spectrum of 127I129I and 129I2

An extensive rotational analysis of the vibrational levels of the XO_g⁺ state of ¹²⁷I¹²⁹I (5 ≤ v″ ≤ 110) and ¹²⁹I₂ (4 ≤ v″ ≤ 108) has been done from laser-induced-fluorescence analyzed with a Fourier transform spectrometer. The usual Dunham relationships are checked. For the range explored the lines can be recalculated with an accuracy better than 0.010 cm⁻¹ and even 0.005 cm⁻¹ for low J values. Checks are done from absolute hyperfine measurements.     

Preparation of Zn2+–Ni2+–Fe3+–CO32−LDHs and study of photocatalytic activities for decomposition of Methyl Orange solution

New type photocatalytic materials of Zn²⁺–Ni²⁺–Fe³⁺–CO₃^2?LDHs were prepared by complexing agent-assisted homogeneous precipitation technique and Zn(NO₃)₂·6H₂O, Ni(NO₃)·6H₂O, Fe(NO₃)₃·9H₂O used as raw materials in the case of molar ratio of Zn²⁺/Ni²⁺/Fe³⁺ = 1:6:2. Zn²⁺–Ni²⁺–Fe³⁺–CO₃^2?LDHs having a specific surface area of 96.5 m²/g. The structure and catalytic properties of the material were systematically studied. The experimental results show that the Zn²⁺–Ni²⁺–Fe³⁺–CO₃^2?LDHs has a higher adsorption performance and lower band gap which make it an excellent catalyst for reducing the degradation of the methyl orange. Study on the process of photocatalytic reaction shows that Methyl Orange was adsorbed to the layer of Zn²⁺–Ni²⁺–Fe³⁺–CO₃^2?LDHs, and then it was photodecomposed to inorganic molecules and ions by Zn²⁺, Ni²⁺, and Fe³⁺ on the surface of Zn²⁺–Ni²⁺–Fe³⁺–CO₃^2?LDHs.