Radiolysis of water vapor in a wide range radiolysis source of a mass spectrometer. I. Individual and total cross sections for the production of positive ions, negative ions, and free radicals by electrons

1970 ◽  
Vol 74 (3) ◽  
pp. 582-587 ◽  
Author(s):  
Charles E. Melton
Author(s):  
Zineb Felfli ◽  
Kelvin Suggs ◽  
Nantambu Nicholas ◽  
Alfred Z. Msezane

We first explore negative-ion formation in fullerenes C44, C60, C70, C98, C112, C120, C132 and C136 through low-energy electron elastic scattering total cross sections calculations using our Regge-pole methodology. Water oxidation to peroxide and water synthesis from H2 and O2 are then investigated using the anionic catalysts C44ˉ to C136ˉ. The fundamental mechanism underlying negative-ion catalysis involves hydrogen bond strength-weakening in the transition state. DFT transition state calculations found C60ˉ numerically stable for both water and peroxide synthesis, C100ˉ increases the energy barrier the most and C136ˉ the most effective catalyst in both water synthesis and oxidation to H2O2.


1999 ◽  
Vol 52 (3) ◽  
pp. 473 ◽  
Author(s):  
S. J. Buckman ◽  
D. T. Alle ◽  
M. J. Brennan ◽  
P. D. Burrow ◽  
J. C. Gibson ◽  
...  

Transient negative ions (resonances) formed during the collision of an electron with an atom or molecule have been extensively studied for over thirty years. The continued interest in these states, both experimentally and theoretically, stems from the profound effects that they can have on electron scattering cross sections and the role that electron–electron correlations play in their formation and quasi-stability. A selective discussion of examples of such resonances, involving one, two and three excited electrons is given for a wide range of atomic and molecular systems.


1956 ◽  
Vol 34 (6) ◽  
pp. 701-715 ◽  
Author(s):  
F. P. Lossing ◽  
D. G. H. Marsden ◽  
J. B. Farmer

The mercury photosensitized (Hg3P1) decomposition of olefins has been examined using a reactor coupled directly to a mass spectrometer. The primary split of ethylene has been shown to be predominantly molecular, and that of propylene mainly into an allyl radical and a hydrogen atom. With 1-butene the split is predominantly at a C–C bond giving allyl and methyl radicals, although a rupture of a C–H bond occurs as well. With 2-butene and isobutene a C–H bond is broken. It is concluded that the allyl and methallyl radicals produced have large cross sections for reaction with excited mercury atoms.


2020 ◽  
Vol 21 (9) ◽  
pp. 3159
Author(s):  
Zineb Felfli ◽  
Kelvin Suggs ◽  
Nantambu Nicholas ◽  
Alfred Z. Msezane

We first explore negative-ion formation in fullerenes C44 to C136 through low-energy electron elastic scattering total cross sections calculations using our Regge-pole methodology. Then, the formed negative ions C44ˉ to C136ˉ are used to investigate the catalysis of water oxidation to peroxide and water synthesis from H2 and O2. The exploited fundamental mechanism underlying negative-ion catalysis involves hydrogen bond strength-weakening/breaking in the transition state. Density Functional Theory transition state calculations found C60ˉ optimal for both water and peroxide synthesis, C100ˉ increases the energy barrier the most, and C136ˉ the most effective catalyst in both water synthesis and oxidation to H2O2.


2017 ◽  
Vol 35 (3) ◽  
pp. 391-396 ◽  
Author(s):  
W. Zhang ◽  
R. Shen ◽  
Y. Ye ◽  
L. Wu ◽  
P. Zhu ◽  
...  

AbstractAn experimental investigation into laser ablation of secondary explosives, cyclotetramethylene tetranitramine (HMX), has been carried out by using a solid-state laser at the wavelength of 1064 nm. The ion particles of decomposition were detected by using a time-of-flight mass spectrometer. Possible attributions of both negative ions and positive ions were obtained. Some obvious peaks were found atm/z= 18, 28, 46, 60, and 106, corresponding to H2O, CO/N2/H2CN, NO2, CH2NO2/N2O2, and N(NO2)2/CH2(NO2)2, respectively. According to the distribution of the particles, three possible pathways were proposed to explain the process of particles. The results may shed some light on the possible decomposition mechanism of HMX under laser initiation.


2016 ◽  
Vol 94 (4) ◽  
pp. 431-436
Author(s):  
S.A. Elkilany

Inelastic collisions of protons with rubidium atoms are treated for the first time within the framework of the three channel coupled static, and frozen core approximations. The method is used for calculating partial and total cross sections with the assumption that only three channels (elastic; non-excited hydrogen, 1s-state; and excited hydrogen, 2s-state) are open. We have used the Lipmann–Schwinger equation and the Green’s functions iterative numerical method technique to solve the derived coupled integro-differential equations to obtain the computer code. The present results for total hydrogen formation cross sections are in agreement with results of other available ones in a wide range of incident energy.


In the previous paper it has been shown that the negative ions found in hydrogen, nitrogen, oxygen, and carbon dioxide are formed from positive ions which acquire two electrons from a negatively-charged surface, and are then accelerated away from the surface as negative ions. It will be shown in this paper that the negative ions come off the surface on which they are formed with a wide range of energy, extending from zero up to beyond 60 volts for O - and beyond 109 volts for H - . This energy is derived from the parent positive ions which have 200 volts’ kinetic energy on striking the surface.


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