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Krypton, ionization potential

The difference in the ionization potentials of xenon and krypton (1170 versus 1351 kj/mol) indicates that krypton should be the less the reactive of the two. Some indication of the difference can be seen from the bond energies, which are 133 kj/mol for the Xe-F bond but only 50 kj/mol for the Kr-F bond. As a result, XeF2 is considerably more stable of the difluorides, and KrF2 is much more reactive. Krypton difluoride has been prepared from the elements, but only at low temperature using electric discharge. When irradiated with ultraviolet light, a mixture of liquid krypton and fluorine reacts to produce KF2. As expected, radon difluoride can be obtained, but because all isotopes of radon undergo rapid decay, there is not much interest in the compound. In this survey of noble gas chemistry, the... [Pg.566]

The density dependence of Vg in Kr was determined by field ionization of CH3I [62] and (0113)28 [63]. Whereas previous studies found a minimum in Vg at a density of 12 X 10 cm [66], the new study indicates that the minimum is at 14.4 x 10 cm (see Fig. 3). This is very close to the density of 14.1 x 10 cm at which the electron mobility reaches a maximum in krypton [67], a result that is consistent with the deformation potential model [68] which predicts the mobility maximum to occur at a density where Vg is a minimum. The use of (0113)28 permitted similar measurements of Vg in Xe because of its lower ionization potential. The results for Xe are also shown in Fig. 3 by the lower line. [Pg.181]

Fig. 2. Ionization potentials of certain species and the energies of argon, krypton, and... Fig. 2. Ionization potentials of certain species and the energies of argon, krypton, and...
From a comparison of their ionization potentials, one would expect that krypton would form compounds with more difficulty than would xenon and this is the case. The difluoiide of... [Pg.404]

Within a year of the discovery of XePtFe and as a result of worldwide activity, it was clear that the chemistry of the noble gases would be limited to the heavier elements as set out in my Noranda Lecture (see Ref. S2). Because of the dangerous radioactivity associated with all of the radon isotopes, this meant that the bulk of noble-gas chemistry would be that of xenon. The chemistry of krypton appeared to be limited to KrF2 and compounds that could be derived from it. In all cases, it was clear, the range of accessible noble-gas chemistry was dictated by lower ionization potentials at the noble-gas atom, and high electronegativity and small size of the ligand atoms, as discussed in Ref. 45. [Pg.198]

Nature of Ion Injected into Liquid Isobutylene. The krypton resonance lamp emits photons at 1236 A. (10.0 e.v.) and 1165 A. (10.6 e.v.) with relative intensities of 1.00 and 0.28 respectively (5). The ionization potential of isobutylene is 9.4 e.v., and the lowest appearance potential for a fragment ion from isobutylene is 11.3 e.v. (C4H7+) (I). Therefore, the only ion produced is the parent C4H8+. [Pg.369]

The relative product distribution produced by photons of 10-e.v. energy in the krypton resonance radiation photolysis will also be taken as representative of excited neutral decomposition induced by electron impact at energies exceeding the ionization potential of ethyl chloride (10.9 e.v.). That is, the contribution to the radiolysis products from excited neutral molecule decomposition will be assumed to have the same relative distribution as that observed in the photolytic decomposition. While superexcited molecules will also be produced in the radiolysis, there is considerable evidence to support the view that their modes... [Pg.430]

The relative density of solid argon is 1-7 and of solid krypton is 3 2, and both adopt the same crystal structure. From these data, the atomic weights, and the data for polarizabilities and ionization potentials in Table 4.1 calculate the binding energy of krypton from that of argon shown in Table 4.1. [Pg.35]

Prior to 1962 the rare gases were frequently called inert gases as no chemical compounds were known (there were a few clathrates and hydrates ), but the realization that the ionization potential of xenon was sufficiently low to be accessible to chemical reaction led to the preparation of several fluorides, oxides, oxyfluorides, and a hexafluoroplatinate of xenon. Several unstable krypton and radon compounds have been synthesized. [Pg.233]

Argon (Ar) gas, for example, is over 30 times more abundant than carbon dioxide and, therefore, not rare. And xenon is not inert it s first compounds were created in 1962. When xenon (Xe) forms binary fluorides and oxides as well as fluoride complexes and oxoanions, the stability of these compounds is very low. It s reactivity is related to increasing atomic size as you go down the table, which leads to a decrease in the first ionization potentials. Xenon tetraflouride (XeF,) is made by mixing one part xenon gas to three parts fluorine gas in a container at 400 °C. Compounds have been confirmed for argon (HArF), krypton (KrF2), xenon (numerous fluorides, oxyfluorides, and oxides), and radon (RnF2). It s believed that compounds exist with helium and neon as well, though none have been experimentally proven to date. [Pg.204]

The setup for atmospheric pressure photoionization (APPI) (Bos et ah, 2006 Hanold et ah, 2004 Raffaelli and Saba, 2003 Robb et ah, 2000) is very similar to that of APCI (Fig. 8.7). Only the corona discharge is replaced by a gas discharge lamp (krypton,10.0 eV) that generates ultraviolet (UV) photons in vacuum. The liquid phase is also vaporized by a pneumatic nebulizer and different geometries are used. Most analytes have ionization potentials below 10 eV, while high-pressure liquid chromatography (HPLC) solvents have higher ionization potentials (water 12.6 eV, methanol 10.8 eV, and acetonitrile 12.2 eV). [Pg.269]


See other pages where Krypton, ionization potential is mentioned: [Pg.25]    [Pg.45]    [Pg.566]    [Pg.482]    [Pg.19]    [Pg.369]    [Pg.30]    [Pg.904]    [Pg.121]    [Pg.401]    [Pg.57]    [Pg.3136]    [Pg.46]    [Pg.238]    [Pg.33]    [Pg.393]    [Pg.169]    [Pg.144]    [Pg.137]    [Pg.57]    [Pg.57]    [Pg.3135]    [Pg.233]    [Pg.187]    [Pg.373]    [Pg.64]    [Pg.2166]    [Pg.300]    [Pg.23]    [Pg.1090]    [Pg.144]    [Pg.350]    [Pg.322]    [Pg.199]    [Pg.154]    [Pg.403]    [Pg.475]    [Pg.612]   
See also in sourсe #XX -- [ Pg.80 ]




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