Single ionization of an asymmetric diatomic system by relativistic charged projectiles

2021 ◽  
Vol 103 (4) ◽  
Author(s):  
A. Jacob ◽  
C. Müller ◽  
A. B. Voitkiv
Atoms ◽  
2021 ◽  
Vol 9 (2) ◽  
pp. 31
Author(s):  
Ghanshyam Purohit

We report triple differential cross-sections (TDCSs) for the electron impact single ionization of tungsten atoms for the ionization taking place from the outer sub shells of tungsten atoms, viz. W (6s), W (5d), W (5p) and W (4f). The study of the electron-induced processes such as ionization, excitation, autoionization from tungsten and its charged states is strongly required to diagnose and model the fusion plasma in magnetic devices such as Tokamaks. Particularly, the cross-section data are important to understand the electron spectroscopy involved in the fusion plasma. In the present study, we report TDCS results for the ionization of W atoms at 200, 500 and 1000 eV projectile energy at different values of scattered electron angles. It was observed that the trends of TDCSs for W (5d) are significantly different from the trends of TDCSs for W (6s), W (5p) and W (4f). It was further observed that the TDCS for W atoms has sensitive dependence on value of momentum transfer and projectile energy.


Atoms ◽  
2021 ◽  
Vol 9 (1) ◽  
pp. 3
Author(s):  
Juan M. Monti ◽  
Michele A. Quinto ◽  
Roberto D. Rivarola

A complete form of the post version of the continuum distorted wave (CDW) theory is used to investigate the single ionization of multielectronic atoms by fast bare heavy ion beams. The influence of the non-ionized electrons on the dynamic evolution is included through a residual target potential considered as a non-Coulomb central potential through a GSZ parametric one. Divergences found in the transition amplitude containing the short-range part of the target potential are avoided by considering, in that term exclusively, an eikonal phase instead of the continuum factor as the initial channel distortion function. In this way, we achieve the inclusion of the interaction between the target active electron and the residual target, giving place to a more complete theory. The present analysis is supported by comparisons with existing experimental electron emission spectra and other distorted wave theories.


1998 ◽  
Vol 31 (22) ◽  
pp. 4961-4973
Author(s):  
K Lozhkin ◽  
B Fastrup ◽  
A D González ◽  
E Horsdal-Pedersen ◽  
V D Rodríguez
Keyword(s):  

1996 ◽  
Vol 74 (7-8) ◽  
pp. 373-375 ◽  
Author(s):  
R. Hippler ◽  
S. Helms ◽  
U. Brinkmann ◽  
J. Deiwiks ◽  
H. Schneider ◽  
...  

Recent experimental results for the multiple ionization of argon by positron impact have been reanalysed. Absolute cross sections for the double and triple ionization of argon were obtained from measured ratios of double-to-single and triple-to-single ionization, using known cross sections for single ionization and for positronium formation. Distinct differences compared to similar results for electron impact are noted.


1986 ◽  
Vol 64 (4) ◽  
pp. 323-327 ◽  
Author(s):  
Mohammed A. Kashem ◽  
H. Brian Dunford

The transient state kinetics of the oxidation of reduced nicotinamide adenine dinucleotide (NADH) by horseradish peroxidase compound I and II (HRP-I and HRP-II) was investigated as a function of pH at 25.0 °C in aqueous solutions of ionic strength 0.11 using both a stopped-flow apparatus and a conventional spectrophotometer. In agreement with studies using many other substrates, the pH dependence of the HRP-I–NADH reaction can be explained in terms of a single ionization of pKa = 4.7 ± 0.5 at the active site of HRP-I. Contrary to studies with other substrates, the pH dependence of the HRP-H–NADH reaction can be interpreted in terms of a single ionization with pKa of 4.2 ± 1.4 at the active site of HRP-II. An apparent reversibility of the HRP-II–NADH reaction was observed. Over the pH range of 4–10 the rate constant for the reaction of HRP-I with NADH varied from 2.6 × 105 to5.6 × 102 M−1 s−1 and of HRP-II with NADH varied from 4.4 × 104 to 4.1 M−1 s−1. These rate constants must be taken into consideration to explain quantitatively the oxidase reaction of horseradish peroxidase with NADH.


2004 ◽  
Vol 37 (8) ◽  
pp. 1565-1580 ◽  
Author(s):  
M Foster ◽  
D H Madison ◽  
J L Peacher ◽  
M Schulz ◽  
S Jones ◽  
...  

2010 ◽  
Vol 104 (16) ◽  
Author(s):  
O. G. de Lucio ◽  
S. Otranto ◽  
R. E. Olson ◽  
R. D. DuBois

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