Kinetics of electron attachment to OH and HNO3 and mutual neutralization of Ar+ with NO2(-) and NO3(-) at 300 and 500 K

The electron attachment rate constant to nitric acid (HNO(3)) has been measured in a flowing afterglow-Langmuir probe (FALP) apparatus at 300 and 500 K using three independent methods: the traditional FALP technique of monitoring electron depletion, "one-gas" VENDAMS (variable electron and neutral density attachment mass spectrometry), and "two-gas" VENDAMS. The three measurements are in agreement with a 300 K weighted average of 1.4 ± 0.3 × 10(-7) cm(3) s(-1), 2 to 10 times higher than previously reported values. Attachment is primarily dissociative yielding NO(2)(-) as previously reported, but for the first time a small endothermic channel to produce OH(-) was also observed at 500 K. From the one-gas VENDAMS data, associative attachment to the OH produced in the primary attachment was found to occur with an effective two body rate constant of 1.2±(0.7) (3)×10(-11) cm(3) s(-1) at 300 K, the first reported rate constant for this radical species. Finally, ion-ion neutralization rate constants of NO(2)(-) and NO(3)(-) with Ar(+) were determined to be 5.2±(2.5) (1.5) × 10(-8) and 4.5 ± 2.5 × 10(-8) cm(3) s(-1) at 300 K, respectively.     

Clusters of sulfur and selenium in nanoporous carbon

The results of x-ray diffraction, x-ray photoelectron spectroscopy, electrical, and galvanomagnetic studies of nanoporous carbon with sulfur and selenium nanoclusters introduced into pores are analyzed. Conclusions are drawn concerning the short-range order in the introduced clusters and their interaction with carbon.     

Photoluminescence of SiO<Subscript>2</Subscript> layers prepared on β-SiC films and an analysis of their elemental composition

The spectra of pulsed time-resolved photoluminescence of oxidized films prepared through electrochemical oxidation on SiC/Si films are investigated. The elemental composition of the films is analyzed using Rutherford backscattering and nuclear reactions. It is revealed that a certain part of the carbon atoms remain in the oxide. The specific features of the parameters of the spectral bands and their kinetics with time are explained by the presence of carbon uniformly distributed throughout the oxide. The structure of oxides at different oxidation times is examined with the use of electron microscopy. Conclusions are drawn regarding possible photoluminescence centers.     

The importance of NO+ (H2O)4 in the conversion of NO+ (H2O)n to H3O+ (H2O)n: I. Kinetics measurements and statistical rate modeling

The kinetics for conversion of NO(+)(H(2)O)(n) to H(3)O(+)(H(2)O)(n) has been investigated as a function of temperature from 150 to 400 K. In contrast to previous studies, which show that the conversion goes completely through a reaction of NO(+)(H(2)O)(3), the present results show that NO(+)(H(2)O)(4) plays an increasing role in the conversion as the temperature is lowered. Rate constants are derived for the clustering of H(2)O to NO(+)(H(2)O)(1-3) and the reactions of NO(+)(H(2)O)(3,4) with H(2)O to form H(3)O(+)(H(2)O)(2,3), respectively. In addition, thermal dissociation of NO(+)(H(2)O)(4) to lose HNO(2) was also found to be important. The rate constants for the clustering increase substantially with the lowering of the temperature. Flux calculations show that NO(+)(H(2)O)(4) accounts for over 99% of the conversion at 150 K and even 20% at 300 K, although it is too small to be detectable. The experimental data are complimented by modeling of the falloff curves for the clustering reactions. The modeling shows that, for many of the conditions, the data correspond to the falloff regime of third body association.     

Many-body ionization in a frozen Rydberg gas

In a dense gas of 300 microK 85Rb atoms of n approximately 50 ionization occurs on a 100 ns time scale, far too fast to be explained by the motion of the atoms or photoionization by 300 K blackbody radiation. Rapid ionization is accompanied by spectral broadening, with the spectrum becoming continuous at n=88 at a density of 5x10(10)cm(-3). The atomic transitions broaden both smoothly and by the emergence of new features, which we attribute to multiple atom absorptions. We attribute the rapid ionization to a sequence of near resonant dipole-dipole transitions through virtual states in this intrinsically many-body system, culminating in the ionization of some of the atoms.