Infrared emission bands from transitions between excited states of cesium–noble gas molecules

1979 ◽  
Vol 71 (10) ◽  
pp. 4052-4056 ◽  
Author(s):  
R. Novak ◽  
N. D. Bhaskar ◽  
W. Happer
Keyword(s):  
Excited States ◽  
Noble Gas ◽  
Infrared Emission ◽  
Gas Molecules

Theoretical prediction of new noble-gas molecules FNgBNR (Ng = Ar, Kr, and Xe; R = H, CH3, CCH, CHCH2, F, and OH)

2013 ◽  
Vol 15 (24) ◽  
pp. 9701 ◽  
Author(s):  
Jien-Lian Chen ◽  
Chang-Yu Yang ◽  
Hsiao-Jing Lin ◽  
Wei-Ping Hu
Keyword(s):  
Theoretical Prediction ◽  
Noble Gas ◽  
Gas Molecules

scholarly journals Emission of Noble Gases Binary Mixtures under Excitation by the Products of the 6Li (n, α)3 H Nuclear Reaction

2020 ◽  
Vol 2020 ◽  
pp. 1-7
Author(s):  
Kuanysh Samarkhanov ◽  
Mendykhan Khasenov ◽  
Erlan Batyrbekov ◽  
Inesh Kenzhina ◽  
Yerzhan Sapatayev ◽  
...  
Keyword(s):  
Nuclear Reaction ◽  
Nuclear Energy ◽  
Alkali Metals ◽  
Nuclear Reactor ◽  
Noble Gases ◽  
Noble Gas ◽  
Direct Conversion ◽  
Reaction Products ◽  
Gas Molecules ◽  
Sodium And Potassium

The luminescence of Kr-Xe, Ar-Kr, and Ar-Xe mixtures was studied in the spectral range 300–970 nm when excited by 6Li (n, α)3 H nuclear reaction products in the core of a nuclear reactor. Lithium was deposited on walls of experimental cell in the form of a capillary-porous structure, which made it possible to measure up to a temperature of 730 K. The temperature dependence of the radiation intensity of noble gas atoms, alkali metals, and heteronuclear ionic noble gas molecules was studied. Also, as in the case of single-component gases, the appearance of lithium lines and impurities of sodium and potassium is associated with vaporization during the release of nuclear reaction products from the lithium layer. The excitation of lithium atoms occurs mainly as a result of the Penning process of lithium atoms on noble gas atoms in the 1s states and subsequent ion-molecular reactions. Simultaneous radiation at transitions of atoms of noble gases and lithium, heteronuclear ion molecules of noble gases allows us to increase the efficiency of direct conversion of nuclear energy into light.

Selective Emergence of the Halogen Bond in Ground and Excited States of Noble‐Gas–Chlorine Systems

2019 ◽  
Vol 131 (13) ◽  
pp. 4239-4243 ◽  
Author(s):  
Fernando Pirani ◽  
David Cappelletti ◽  
Stefano Falcinelli ◽  
Diego Cesario ◽  
Francesca Nunzi ◽  
...  
Keyword(s):  
Excited States ◽  
Halogen Bond ◽  
Noble Gas

Absorption spectrum of the NO molecule. VIII. The heterogeneous (2Σ–2Π) interactions between excited states

1968 ◽  
Vol 46 (8) ◽  
pp. 987-1003 ◽  
Author(s):  
Ch. Jungen ◽  
E. Miescher
Keyword(s):  
Absorption Spectrum ◽  
High Resolution ◽  
Excited States ◽  
Rydberg State ◽  
Vacuum Ultraviolet ◽  
Principal Quantum Number ◽  
Rydberg States ◽  
Infrared Emission ◽  
Strong Interactions ◽  
Rydberg Series

Heterogeneous perturbations 2E+ ~ 2Π of largely different magnitudes are observed with high resolution in the vacuum-ultraviolet absorption and in the infrared emission spectrum of the NO molecule. The rotational interactions between 2Σ+ Rydberg states and levels of the B2Π non-Rydberg state are shown to be "configurationally forbidden", but produced by the configuration interaction between the non-Rydberg levels and 2Π Rydberg states. The latter together with the 2Σ+ Rydberg states form p complexes. In this way the interactions display the l uncoupling in the complexes; they can be evaluated theoretically and can be analyzed fully. The cases of the strong interactions D2Σ+(v = 3) ~ B2Π(v = 16)and D2Σ+(v = 5) ~ B2Π(v = 21) and of the weaker D2Σ+(v = 1) ~ B2Π(v = 11), all three observed as perturbations in ε bands crossing 3 bands, are discussed in detail. It is further shown that perturbations between γ bands and β bands as well as perturbations between analogous bands of higher principal quantum number are absent, and thus the assignment of the A2Σ+ and E2Σ+ states to the s Rydberg series is confirmed.

scholarly journals Formation of Potential Interstellar Noble Gas Molecules in Gas and Adsorbed Phases

ACS Omega ◽  
2016 ◽  
Vol 1 (5) ◽  
pp. 765-772 ◽  
Author(s):  
Gerald T. Filipek ◽  
Ryan C. Fortenberry
Keyword(s):  
Noble Gas ◽  
Gas Molecules

THE HYDROGEN–CHLORINE SYSTEM IN THE MM PRESSURE RANGE: I. ENERGY DISTRIBUTION AMONG VIBRATIONALLY EXCITED STATES

1964 ◽  
Vol 42 (10) ◽  
pp. 2176-2192 ◽  
Author(s):  
F. D. Findlay ◽  
J. C. Polanyi
Keyword(s):  
Excited States ◽  
Rotational Temperature ◽  
Relative Rate ◽  
Infrared Emission ◽  
Vibrational States ◽  
Vibrationally Excited ◽  
Experimental Conditions ◽  
Reduced Pressure ◽  
A Chain ◽  
First Time

When atomic plus molecular hydrogen coming from a Wood's discharge tube are mixed with molecular chlorine, infrared emission is observed (1). At low reagent pressures, ~10−2 mm Hg, this emission can be related to the relative rate of the reaction H + Cl2 → HCl†ν + Cl proceeding to form HCl in vibrationally excited states ν = 1–6, of the ground electronic state. In the present work this system has been investigated for the first time at ~100 × the reagent pressure (~1 mm Hg). The reaction was shown to proceed by a chain mechanism. The translational–rotational temperature was 1300 ± 100 °K under the experimental conditions normally used. The vibrational distribution was notable for the presence of vibrators in levels ν = 7 and 8, which are respectively 4 and 10 kcal higher in energy than the exothermicity of the H + Cl2 reaction. The population in these levels appeared to be related to that in the levels with [Formula: see text]; it was proposed that vibrational–vibrational exchange among these lower levels was responsible for populating the higher ones. A simple model yielded a collision efficiency for HCl†ν=1 + HCl†ν=6 → HCl†ν=7 + HCl†ν=0, of Z1,6t = 6 × 103 collisions per transfer. Addition of HCl to the reaction mixture brought about a redistribution among vibrationally excited states indicative of a fast vibrational transfer, HClν=0 + HCl†ν=2 → 2 HCl†ν=1.At reduced pressure of HCl† the stationary-state distribution among higher vibrational states approximated closely to that observed at 10−2 mm Hg total pressure (where collisional deactivation is insignificant), suggesting that collisional deactivation was not of major importance even at the pressure used in the present work. In order to account for the high translational–rotational temperature, in the absence of substantial vibrational deactivation, it was necessary to suppose that the greater part of the energy liberated by the reaction H + Cl2 went directly into translational and rotational motion of the products.

Stability analysis of the neutral noble gas molecules FNgX and their anions FNgX−(Ng = He, Ar, Kr; X = O, S)

2009 ◽  
Vol 109 (4) ◽  
pp. 782-789 ◽  
Author(s):  
Yun Li ◽  
Hongqi Ai ◽  
Zhongnan Qi ◽  
Wei He ◽  
Liang Zhang
Keyword(s):  
Stability Analysis ◽  
Noble Gas ◽  
Gas Molecules
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