Fast atom bombardment mechanism process

Thus as a starting point for understanding the bombardment process we have developed a classical dynamics procedure to model the motion of atomic nuclei. The predictions of the classical model for the observables can be compared to the data from sputtering, spectrometry (SIMS), fast atom bombardment mass spectrometry (FABMS), and plasma desorption mass spectrometry (PDMS) experiments. In the circumstances where there is favorable agreement between the results from the classical model and experimental data It can be concluded that collision cascades are Important. The classical model then can be used to look at the microscopic processes which are not accessible from experiments In order to give us further insight into the ejection mechanisms. 

A wide variety of desorption ionization methods is available [7] desorption chemical ionization (DCI), secondary-ion mass spectrometry (SIMS), fast-atom bombardment (FAB), liquid-SIMS, plasma desorption (PD), matrix-assisted laser desorption ionization (MALDI), and field desorption (FD). Two processes are important in the ionization mechanism, i.e., the formation of ions in the sample matrix prior to desorption, and rapid evaporation prior to ionization, which can be affected by very rapid heating or by sputtering by high-energy photons or particles. In addition, it is assumed that the energy deposited on the sample surface can cause (gas-phase) ionization reactions to occur near the interface of the solid or liquid and the vacuum (the so-called selvedge) or provide preformed ions in the condensed phase with sufficient kinetic energy to leave their environment. 

Gross and coworkers129 also studied the unimolecular dissociation of protonated acy-lanilines, viz. A-[2-(benzoyloxy)phenyl]benzamides formed via both fast-atom bombardment (FAB) and electrospray ionization (ESI). They found that cyclization occurs upon the loss of a molecule of benzoic acid, and that a similar process occurs for the molecular ion under El. This gas-phase reaction is analogous to a solution reaction leading to phenyl-benzoxazoles. The proposed cyclization process, for which concurrent mechanisms were proposed (Scheme 38 depicts only the displacement reaction route), was corroborated by accurate mass measurements, tandem mass spectrometric experiments with comparison with reference ions, isotopic labeling and theoretical calculations. 

It thus appears that a possible and fast mechanism for the production of ozone is by way of oxygen atoms which act as catalysts for the conversion of 02 O3. Because oxygen atoms are essentially slow in destruction of ozone, the limiting stationary process must be the destruction of ozone via the same type of process which is responsible for oxygen destruction—e.g., electron bombardment—or else the increase in temperature of the discharge which would finally provoke the thermal decomposition of ozone and make Reaction 3 a limiting process. 

---