60Co γ-RADIOLYSIS OF HYDROGEN HALIDES AT 77 °K

1966 ◽  
Vol 44 (2) ◽  
pp. 191-197
Author(s):  
R. C. Rumfeldt ◽  
D. A. Armstrong

Yields of hydrogen formed in the 60Co γ-radiolyses of pure polycrystalline samples of HBr and HCl at 77 °K decrease with increasing dose in the range 0 to 1 × 1018 eV per g. The true initial yields are G(H2)solidHClat77°K = 6.3 ± 0.2 and G(H2)solidHBrat77°K = 12.3 ± 0.3. Within experimental error these are the same as the respective liquid-phase yields at −79 °C. For doses in excess of 2 × 1018 eV per g the dose dependence is no longer significant and the yields tend toward plateau values of 3.2 ± 0.1 and 10.3 ± 0.1 for HCl and HBr respectively. The dose dependence of the hydrogen yields is attributed to the scavenging of a reactive intermediate by the halogen atoms and molecules which accumulate in the solid matrix as the dose increases.In independent experiments with an apparatus of the Klein–Scheer type it was shown that hydrogen atoms react readily with films of HBr at 77 °K. There is, however, no evidence of a significant reaction with HCl at this temperature. The difference in behavior of the two hydrogen halides may be explained by their different activation energies for reaction with hydrogen atoms. The results of the γ-radiolyses are discussed in the light of these experiments and it is suggested that the dose dependence may be a result of the scavenging of an ionic intermediate rather than a thermal hydrogen atom.

2011 ◽  
Vol 03 ◽  
pp. 555-563 ◽  
Author(s):  
YU. V. CHURKIN ◽  
A. B. FEDORTSOV ◽  
G. L. KLIMCHITSKAYA ◽  
V. A. YUROVA

We calculate the interaction energy and force between atoms and molecules and single-walled carbon nanotubes described by the Dirac model of graphene. For this purpose the Lifshitz-type formulas adapted for the case of cylindrical geometry with the help of the proximity force approximation are used. The results obtained are compared with those derived from the hydrodymanic model of graphene. Numerical computations are performed for hydrogen atoms and molecules. It is shown that the Dirac model leads to larger values of the van der Waals force than the hydrodynamic model. For a hydrogen molecule the interaction energy and force computed using both models are larger than for a hydrogen atom.


2011 ◽  
Vol 26 (22) ◽  
pp. 3958-3966 ◽  
Author(s):  
YU. V. CHURKIN ◽  
A. B. FEDORTSOV ◽  
G. L. KLIMCHITSKAYA ◽  
V. A. YUROVA

We calculate the interaction energy and force between atoms and molecules and single-walled carbon nanotubes described by the Dirac model of graphene. For this purpose the Lifshitz-type formulas adapted for the case of cylindrical geometry with the help of the proximity force approximation are used. The results obtained are compared with those derived from the hydrodymanic model of graphene. Numerical computations are performed for hydrogen atoms and molecules. It is shown that the Dirac model leads to larger values of the van der Waals force than the hydrodynamic model. For a hydrogen molecule the interaction energy and force computed using both models are larger than for a hydrogen atom.


1975 ◽  
Vol 53 (8) ◽  
pp. 1237-1244 ◽  
Author(s):  
D. G. Hooper ◽  
M. Simon ◽  
M. H. Back

The ratio of the rate constants for disproportionation and combination for ethyl radicals, kd/kc[Formula: see text]has been measured over the temperature range 298–173 K in the gas phase. Ethyl radicals were produced by direct photolysis of ethylene followed by addition of hydrogen atoms to ethylene. At low temperatures the only important reactions of the radicals were combination and disproportionation. The ratio kd/kc was obtained from measurements of the rates of formation of ethane, butane, and butene. No change in the ratio kd/kc was observed over the temperature range studied, leading to the conclusion that Ed − Ec = 0, within the experimental error. The significance of this result is discussed in relation to other measurements in both gas and liquid phase and to the nature of the transition state for this reaction.


2019 ◽  
Vol 484 (1) ◽  
pp. 56-60
Author(s):  
D. A. Indejtsev ◽  
E. V. Osipova

Hydrogen atom behavior in pure aluminum is described by ab initio modelling. All main energy characteristics of the system consisting of hydrogen atoms in a periodic aluminum crystal are found.


Crystals ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 189 ◽  
Author(s):  
Sandra Witkiewicz-Lukaszek ◽  
Anna Mrozik ◽  
Vitalii Gorbenko ◽  
Tetiana Zorenko ◽  
Pawel Bilski ◽  
...  

This work is dedicated to the development of new types of composite thermoluminescent (TL) detectors for simultaneous registration of the different components of ionization radiation based on the single crystalline films (SCFs) of Ce3+-doped Lu3−xGdxAl5O12:Ce (x = 0–1.5) garnet and Y3Al5O12:Ce (YAG:Ce) substrates using the liquid phase epitaxy (LPE) growth method. For this purpose, the TL properties of the mentioned epitaxial structures were examined in Risø TL/OSL-DA-20 reader under excitation by α- and β-particles from 242Am and 90Sr-90Y sources. We have shown that the cation engineering of SCF content can result in more significant separation of the TL glow curves of SCFs and substrates under α- and β-particle excitations in comparison with the prototype of such composite detectors based on the Lu3Al5O12:Ce (LuAG:Ce)/YAG:Ce epitaxial structure. Specifically, the difference between the TL glow curves of Lu1.5Gd1.5Al5O12:Ce SCFs and YAG:Ce substrates increases up to 120 K in comparison with a respective value of 80 degrees in the prototype based on the LuAG:Ce/YAG:Ce epitaxial structure. Therefore, the LPE-grown epitaxial structures containing Lu1.5Gd1.5Al5O12:Ce SCFs and Ce3+-doped YAG:Ce substrate can be successfully applied for simultaneous registration of α- and β-particles in mixed fluxes of ionization radiation.


1971 ◽  
Vol 49 (12) ◽  
pp. 2178-2182 ◽  
Author(s):  
J. A. Howard ◽  
S. Korcek

Absolute rate constants for the liquid phase autoxidation of some organic sulfides at 30 °C have been measured. The reactivities of organic sulfides towards t-butylperoxy radicals are equal to or somewhat less than the reactivities of structurally analogous ethers. The α-alkylthiylalkylperoxy radicals appear to be about 3–5 times more reactive in hydrogen atom abstraction than the α-alkoxyalkylperoxy radicals.


1969 ◽  
Vol 17 (2) ◽  
pp. 458-461 ◽  
Author(s):  
Bruce McCarroll ◽  
John R. Anderson

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