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Impact ionization

Coincidence experiments explicitly require knowledge of the time correlation between two events. Consider the example of electron impact ionization of an atom, figure Bl.10.7. A single incident electron strikes a target atom or molecule and ejects an electron from it. The incident electron is deflected by the collision and is identified as the scattered electron. Since the scattered and ejected electrons arise from the same event, there is a time correlation... [Pg.1428]

Figure Bl.10.7. Electron impact ionization coincidence experiment. The experiment consists of a source of incident electrons, a target gas sample and two electron detectors, one for the scattered electron, the other for the ejected electron. The detectors are coimected tlirough preamplifiers to the inputs (start and stop) of a time-to-amplitiide converter (TAC). The output of the TAC goes to a pulse-height-analyser (PHA) and then to a nuiltichaimel analyser (MCA) or computer. Figure Bl.10.7. Electron impact ionization coincidence experiment. The experiment consists of a source of incident electrons, a target gas sample and two electron detectors, one for the scattered electron, the other for the ejected electron. The detectors are coimected tlirough preamplifiers to the inputs (start and stop) of a time-to-amplitiide converter (TAC). The output of the TAC goes to a pulse-height-analyser (PHA) and then to a nuiltichaimel analyser (MCA) or computer.
It is well known that the electron-impact ionization mass spectrum contains both the parent and fragment ions. The observed fragmentation pattern can be usefiil in identifying the parent molecule. This ion fragmentation also occurs with mass spectrometric detection of reaction products and can cause problems with identification of the products. This problem can be exacerbated in the mass spectrometric detection of reaction products because diese internally excited molecules can have very different fragmentation patterns than themial molecules. The parent molecules associated with the various fragment ions can usually be sorted out by comparison of the angular distributions of the detected ions [8]. [Pg.2070]

Molecular Identification. In the identification of a compound, the most important information is the molecular weight. The mass spectrometer is able to provide this information, often to four decimal places. One assumes that no ions heavier than the molecular ion form when using electron-impact ionization. The chemical ionization spectrum will often show a cluster around the nominal molecular weight. [Pg.812]

The mass spectrum is a fingerprint for each compound because no two molecules are fragmented and ionized in exactly the same manner on electron-impact ionization. In reporting mass spectra the data are normalized by assigning the most intense peak (denoted as base peak) a value of 100. Other peaks are reported as percentages of the base peak. [Pg.815]

At still higher fields carriers can acquke enough energy from motion in an electric field to create electron—hole paks by impact ionization. Eor siUcon the electron ioniza tion rate, which is the number of paks generated per cm of electron travel, depends exponentially on electric field. It is about 2 X 10 cm for a 50 kV/cm field at 300 K. The electric field causes electrons and holes so created to travel in opposite dkections. They may create other electron—hole paks causing positive feedback, which leads to avalanche breakdown at sufficiently high fields. [Pg.346]

Physical Chemical Characterization. Thiamine, its derivatives, and its degradation products have been fully characterized by spectroscopic methods (9,10). The ultraviolet spectmm of thiamine shows pH-dependent maxima (11). H, and nuclear magnetic resonance spectra show protonation occurs at the 1-nitrogen, and not the 4-amino position (12—14). The H spectmm in D2O shows no resonance for the thiazole 2-hydrogen, as this is acidic and readily exchanged via formation of the thiazole yUd (13) an important intermediate in the biochemical functions of thiamine. Recent work has revised the piC values for the two ionization reactions to 4.8 and 18 respectively (9,10,15). The mass spectmm of thiamine hydrochloride shows no molecular ion under standard electron impact ionization conditions, but fast atom bombardment and chemical ionization allow observation of both an intense peak for the patent cation and its major fragmentation ion, the pyrimidinylmethyl cation (16). [Pg.85]

Static eliminating devices that ionize the atmosphere around the device are available. Static eliminators are divided into two main groups silent (corona) discharge eliminators, such as inductive eliminators, or high voltage eliminators which initiate an impact ionization of the air by applying strong electrostatic fields, and radioactive eliminators that provide a multitude of ions from independent ion sources (9). [Pg.289]

Similar detailed studies of RSFs have been carried out for GDMS, but not for electron-gun electron impact ionization or for SALI. The spread in elemental RSFs for electron-gas SNMS is comparable to that observed for Ar glow-discharge ionization of sputtered neutrals. ... [Pg.576]

Fig. 2.18. Electron-impact ionization cross-section for the Ni K shell, as a function of reduced electron energy U [2.128] U = Ep/Ek, where Ep is the primary electron energy and E Fig. 2.18. Electron-impact ionization cross-section for the Ni K shell, as a function of reduced electron energy U [2.128] U = Ep/Ek, where Ep is the primary electron energy and E <the binding energy ofthe K shell, (a) experimental points, (b) semi-empirical or theoretical curves.
The cross-section for electron impact ionization has already been mentioned in Sect. 2.2.2.2 in connection with electron sources, and a variety of experimental and theoretical cross-sections have been shown in Fig. 2.18 for the particular case of the K-shell of nickel. The expression for the cross-section derived by Casnati et al. [2.128] gives reasonably good agreement with experiment the earlier expression of Gry-zinski [2.131] is also useful. [Pg.40]

Fig. 3.31. Distributions (i)/(Ee) dEe of electron energy (E ) for a low-pressure HF-plasma (suffix pi, Maxwellian with temperature = 80000 K) and an electron beam (suffix eb, simplified to Gaussian shape with 40 eV half-width) (ii) rTx (Ej) ofthe Ej dependent electron impact ionization cross-section for X=Ti... Fig. 3.31. Distributions (i)/(Ee) dEe of electron energy (E ) for a low-pressure HF-plasma (suffix pi, Maxwellian with temperature = 80000 K) and an electron beam (suffix eb, simplified to Gaussian shape with 40 eV half-width) (ii) rTx (Ej) ofthe Ej dependent electron impact ionization cross-section for X=Ti...
In a strong electric field, a free electron acquires enough kinetic energy to cause an impact ionization i.e., an electron impacting on a neutral molecule causes an emission of a new electron, leading to the formation of new electron-ion pair. The new free electron is, in turn, accelerated to a velocity sufficient to cause further ionization. This leads to an avalanche-type generation of free electrons and ions. The electric field provides the necessary energy in such a way that the process can continue without the external radiation which was necessary for the onset of the process. [Pg.1216]

Figure 12.3 Mass spectrum of 2,2-dimethylpropane (C5Hi2 MW = 72). No molecular ion is observed when electron-impact ionization is used. (What do you think is the structure of the M+ peak at m/z = 57 )... Figure 12.3 Mass spectrum of 2,2-dimethylpropane (C5Hi2 MW = 72). No molecular ion is observed when electron-impact ionization is used. (What do you think is the structure of the M+ peak at m/z = 57 )...
There are numerous ionization techniques available to the mass spectrome-trist, but for GC/MS almost all analyses are performed using either electron impact ionization or chemical ionization. [Pg.15]

Electron Impact Ionization Electron impact ionization (ei) is by far the most commonly used ionization method. The effluent from the GC enters... [Pg.15]

Mass Spectra. Obtained by Gillis et al (Ref 104). Field ionization and electron impact ionization mass spectra are given by Brunee et al (Ref 54) Mechanical Properties < Sound Velocity. Hoge (Ref 77) obtained the following ultimate stress as a function of strain rate for machined discs (1.77g/cc) of PETN (all failures were brittle fractures)... [Pg.564]

Some of the problems encountered in the mass spectrometric study of ion-molecule reactions are illustrated in a review of the H2-He system (25). If the spectrometer ion source is used as a reaction chamber, a mixture of H2 and He are subjected to electron impact ionization, and both H2+ and He+ are potential reactant ions. The initial problem is iden-... [Pg.94]

Reactions of Complex Ions. For reactions of systems containing H2 or HD the failure to observe an E 1/2 dependence of reaction cross-section was probably the result of the failure to include all products of ion-molecule reaction in the calculation of the experimental cross-sections. For reactions of complex molecule ions where electron impact ionization probably produces a distribution of vibrationally excited states, kinetic energy transfer can readily open channels which yield products obscured by primary ionization processes. In such cases an E n dependence of cross-section may be determined frequently n = 1 has been found. [Pg.105]

The mass spectrum of 1-torr ethylene in 20-torr He is also shown in in Figure 14. Remembering that the (electron impact) ionization cross-section for ethylene is 20 times higher than that for He, we expect almost... [Pg.241]

Similarly, the thermal sensitivity of sulfur allotropes makes mass spectrometry of elemental sulfur and sulfur-rich compounds difficult especially with the conventional electron impact ionization. Nevertheless, valuable information has been obtained by this technique also. [Pg.33]


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Electron Impact Ionization. Generation of Positive Ions

Electron Impact and Chemical Ionization

Electron impact ionization

Electron impact ionization characterized

Electron impact ionization cross sections

Electron impact ionization cross sections dependence

Electron impact ionization cross sections quantum mechanical

Electron impact ionization description

Electron impact ionization experimental technique

Electron impact ionization library searches

Electron impact ionization mass spectrometry

Electron impact ionization model

Electron impact ionization section plot

Electron impact ionization, mass

Electron impact ionization/quadrupole mass filter

Electron impact ionizer

Electron impact measurements, ionization

Electron impact measurements, ionization energies

Impact Ionization Process

Impact Ionization and Carrier Multiplication

Impact Ionization and Photoionization

Impact ionization mass spectrometers

Impact ionization parameter

Impact of ionization and dissociation on partitioning

Ionization by electron impact

Ionization chamber, electron impact

Ionization, associative electron impact

Ionization, atmospheric pressure electron impact

Mass spectroscopy electron impact ionization

Organic silicon compounds, electron impact ionization

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Photon impact ionization

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Soft electron-impact ionization

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