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Alkanes ionization

Absorption and Emission Spectra of Alkanes, Ionization in the Liquid Phase... [Pg.366]

Table 12.6. Rare Gas and Alkane Ionization Potentials and Polarizabilities and Free Energies for the Kr-Alkane Complex Equilibria at — 90°C... Table 12.6. Rare Gas and Alkane Ionization Potentials and Polarizabilities and Free Energies for the Kr-Alkane Complex Equilibria at — 90°C...
The species produced through ionization of an electron from a ir-orbital (such as from a C-H or a C-C bond of an alkane in mass spectrometry) cannot be represented at all by a connection table, yet the RAMSES notation can account for it as shown in Figure 2-59. [Pg.68]

Acid-catalyzed isomerization reactions of alkanes as well as alkylation and condensation reactions are initiated by protolytic ionization. Available evidence indicates nonlinear but not necessarily triangular... [Pg.163]

The C—H bonds of hydrocarbons show little tendency to ionize and alkanes alkenes and alkynes are all very weak acids The acid dissociation constant for methane for exam pie IS too small to be measured directly but is estimated to be about 10 ° (pK 60)... [Pg.368]

EPA Method 25A is the instrumental analyzer method for determination of total gaseous organic concentration using a flame ionization analyzer. The method apphes to the measurement of total gaseous organic concentration of vapors consisting primarily of alkanes, alkenes, and/or arenes (aromatic hydrocarbons). The concentration is expressed in terms of propane (or other appropriate organic calibration gas) or in terms or carrion. [Pg.2204]

Figure 14.12 Schematic diagram of the Refomiulyser system Inj, split injector Cl, polar capillary column C2, packed column to retain the alcohols C3, packed Porapak column for the separation of the oxygenates C4, non-polar capillary column C5, packed 13X column A/E cap, Tenax trap to retain the ar omatics Olf. trap, cap to retain the olefins Pt, olefins hydrogenatOT A cap, cap to retain the -alkanes FID, flame-ionization detector. Figure 14.12 Schematic diagram of the Refomiulyser system Inj, split injector Cl, polar capillary column C2, packed column to retain the alcohols C3, packed Porapak column for the separation of the oxygenates C4, non-polar capillary column C5, packed 13X column A/E cap, Tenax trap to retain the ar omatics Olf. trap, cap to retain the olefins Pt, olefins hydrogenatOT A cap, cap to retain the -alkanes FID, flame-ionization detector.
Duffield and coworkers65 studied the El- induced mass spectra of five arene- (215-219) and four alkane sulfonylthioureas (220-223) and observed two rearrangement processes, namely loss of S02 from 215-219 and the elimination of ArS02 and RS02 with the thione sulfur atom from 215-223. The other fragmentations involved simple bond cleavages with and without hydrogen transfer (equation 48). The loss of H2S was evident for all the compounds studied except 221 and 222. It was, however, found to be a thermal and not an ionization process. [Pg.158]

When both reactants have comparable ionization potentials, there is a close relationship between the H2 and H2 transfer reactions. For instance, a low efficiency of the H. transfer reaction from the alkane to a neutral olefin molecule (at least in the case of cyclohexane) is paralleled by a low efficiency of the corresponding H2 transfer process. Such a relationship can be accounted for by resonance phenomena. Unfortunately, not enough information is available on those systems where the... [Pg.278]

In this contribution, in order to illustrate tlie importance of shake-up bands for extended systems, we simulate and compare on correlated grounds the ionization spectra of polyethylene and poly acetylene, the most simplest systems one can consider to represent insulating or semi-conducting polymers. Conclusions for the infinite stereoregular chains are drawn by exU apolation of the trends observed with the first terms of the related n-alkane or acene series, CnH2n+2 and CnHn+2. respectively, with n=2, 4, 6 and 8. Our simulations are also compared to X-ray photoionization spectra (7) recorded on gas phase samples of ethylene, butadiene and hexatriene, which provide a clear experimental manisfestation of the construction of correlation bands (8-12). [Pg.78]

These calculations have been conducted on the basis of RHF optimized geometries, considering the 6-31G basis set for the n-alkane compounds (11), and the 6-31G basis set for the polyacene series (12). In both cases, the basis set contention has been checked by comparison with more thorough investigations on small compounds, such as ADC[3] calculations (11a) on n-butane based on the 6-31IG, 6-31G and 6-31G basis, or the MRSDCI ionization spectrum of ethylene as obtained by Murray and Davidson (33) using a 196-CGTO basis set. [Pg.81]

As the reaction temperature is increased, chemiluminescence is observed in the reactions of ozone with aromatic hydrocarbons and even alkanes. Variation of temperature has been used to control the selectivity in a gas chromatography (GC) detector [35], At room temperature, only olefins are detected at a temperature of 150°C, aromatic compounds begin to exhibit a chemiluminescent response and at 250°C alkanes respond, giving the detector a nearly universal response similar to a flame ionization detector (FID). The mechanisms of these reactions are complex and unknown. However, it seems likely that oxygen atoms produced in the thermal decomposition of ozone may play a significant role, as may surface reactions with 03 and O atoms. [Pg.359]

The gaseous atmosphere was then vented through a trap at -78° (to remove most of the benzene vapor) into an evacuated vessel. Samples were removed by gas-tight syringe and injected into a Hewlett-Packard 5790 gas chromatograph, equipped with a U ft, 1/8 in Porapak P column and a flame ionization detector. Use of known samples of hydrocarbons (methane and ethane) established that the minimum detectable amounts of product by this procedure were about 0.5-1 0 % (based on starting Nb complex). Several of the reactions (Mo(CO)g, W(C0)g and Ru (CO) p) gave small amounts (around 1-2 %) of these alkanes only with Cr(C0)g was a substantial yield of hydrocarbon product consistently observed (see below). [Pg.255]

T. K. Dutta and S. Harayama. Time-of-Flight Mass Spectrometric Analysis of High-Molecular-Weight Alkanes in Crude Oil by Silver Nitrate Chemical Ionization after Laser Desorption. Anal. Chem., 73(2001) 864-869. [Pg.79]


See other pages where Alkanes ionization is mentioned: [Pg.96]    [Pg.541]    [Pg.220]    [Pg.189]    [Pg.96]    [Pg.541]    [Pg.220]    [Pg.189]    [Pg.1032]    [Pg.96]    [Pg.314]    [Pg.1304]    [Pg.87]    [Pg.230]    [Pg.270]    [Pg.277]    [Pg.279]    [Pg.77]    [Pg.82]    [Pg.82]    [Pg.90]    [Pg.9]    [Pg.120]    [Pg.639]    [Pg.534]    [Pg.614]    [Pg.68]    [Pg.32]    [Pg.25]    [Pg.378]    [Pg.258]    [Pg.157]    [Pg.175]   
See also in sourсe #XX -- [ Pg.367 ]




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