Formation of regular surface-supported mesostructures with periodicity controlled by chemical reaction rate

We report a LEEM and XPEEM study of the formation of a variety of stationary two-dimensional metallic and oxygen structures in Au and Au + Pd adlayers on Rh(110) during water formation reaction. They result from chemically frozen spinodal decomposition and are created, preserved, or reversibly modified by tuning the reaction conditions. The wavelength of lamellar structures obtained at intermediate metal coverage is found to obey a power scaling law with respect to the reaction rate.     

Antisymmetry of solutions for some weighted elliptic problems

This article concerns the antisymmetry, uniqueness, and monotonicity properties of solutions to some elliptic functionals involving weights and a double well potential. In the one-dimensional case, we introduce the continuous odd rearrangement of an increasing function and we show that it decreases the energy functional when the weights satisfy a certain convexity-type hypothesis. This leads to the antisymmetry or oddness of increasing solutions (and not only of minimizers). We also prove a uniqueness result (which leads to antisymmetry) where a convexity-type condition by Berestycki and Nirenberg on the weights is improved to a monotonicity condition. In addition, we provide with a large class of problems where antisymmetry does not hold. Finally, some rather partial extensions in higher dimensions are also given.     

Stress induced stripe formation in Pd/W(110)

A stress-induced stripe phase of submonolayer Pd on W(110) is observed by low-energy electron microscopy. The temperature dependence of the pattern is explained by the change both in the boundary free energy and elastic relaxation energy due to the increasing boundary width. The stripes are shown to disorder when the correlation length of the condensed phase becomes comparable to its period, while the condensate to lattice-gas transition takes place at a higher temperature, as revealed by low-energy electron diffraction.     

Counterion binding in the aqueous solutions of bile acid salts, as studied by computer simulation methods

We investigate the structural and dynamical properties of counterion binding in sodium cholate and sodium deoxycholate micelles at three different concentration, namely, 30, 90, and 300 mM, by means of molecular dynamics simulations at the atomistic level. The obtained results can resolve a long-standing, apparent contradiction between different experiments that reported discordant values for the degree of counterion binding. Namely, our results suggest that certain experimental techniques, such as freezing point depression, are only sensitive to the contact counterions, and hence, the degree of contact binding of the counterions is measured. On the other hand, in experiments employing, e.g., electrode potential or nuclear magnetic resonance measurements, the solvent-separated counterions also contribute to the signal detected, and hence, the counterions that are measured as bound ones do include the solvent-separated counterions as well.     

Dissociative double photoionization of N2 using synchrotron radiation: appearance energy of the N2+ dication

Photoionization cross sections for the production of the doubly charged ion N2+ from N2 have been measured by means of synchrotron radiation in the photon energy range from 50 to 110 eV. The appearance energy for N2+ has been determined as 55.2+/-0.2 eV, i.e., about 1.3 eV higher than the spectroscopic dissociation limit leading to the charge asymmetric dissociation channel N2+(2P)+N(4S) at 53.9 eV. The onset of a second threshold at 59.9+/-0.2 eV is detected and the energy dependence of photoion intensities near the threshold regions is interpreted in terms of the Wannier theory. The production of the N2+ dication is discussed in terms of direct and indirect mechanisms for dissociative charge asymmetric photoionization and by comparison with the potential energy curves of the intermediate N(2)2+ dication. Experimental evidences for the opening of the Coulomb explosion channel N2++N+ at high photon energies are provided by measuring the kinetic energy release spectra of N2+ fragments at selected photon energies.     

Determination of airborne polycyclic aromatic hydrocarbons at an airport by gas chromatography-mass spectrometry and evaluation of occupational exposure

The aim of this study was to determine airborne polycyclic aromatic hydrocarbons (PAHs) and biphenyl at an airport by gas chromatography-mass spectrometry and to evaluate occupational exposure by environmental monitoring. A total of 12 samplings were carried out in three areas: (1) a handling area where baggage was unloaded manually from vehicles onto conveyor belts (n=5); (2) the runway with plane and motor vehicle traffic (n=5) and (3) a departure lounge (n=2). PAHs levels were in most cases low. The higher levels found refer to naphthalene (130-13,050 ng/m3) and to its methyl-substitutes 2-methylnaphthalene (64-28,500 ng/m3) and 1-methylnaphthalene (24-35,300 ng/m3), and biphenyl (24-1610 ng/m3). A method was used to quantify twenty-four airborne PAHs, and biphenyl, and to detect a variety of other chemical compounds by means of the deconvolution program AMDIS. After sampling air on quartz filter and PUF and XAD-2 sorbents; extraction with dichloromethane, and concentration and purification on silica cartridges, analyses were carried out by gas chromatography-ion trap mass spectrometry. We used 20 deuterated PAHs to quantify both the 24 native PAHs and biphenyl. The native substances had been subdivided into small groups and in this way, their volatility was adequately reflected by the D-PAH present in each group. The limit of detection was 0.1 ng/m3 for all the PAHs, and a linear range of at least about three-fold the maximum level studied (naphthalene) was obtained both for D-PAHs and the native PAHs. A good recovery pattern was obtained for D-PAHs on quartz filters, PUF and XAD-2.