WKB properties of the time-dependent Schrödinger system

It is shown that the time-dependent WKB expansion highlights some of the hidden properties of the Schrödinger equation and forms a natural bridge between that equation and the functional integral formulation of quantum mechanics. In particular it is shown that the leading (zero- and first-order in ) terms in the WKB expansion are essentially classical, and the relationship of this result to the classical nature of the WKB partition function, and of the anomalies in quantum field theory, is discussed.     

Energetic ion bombardment of Ag surfaces by C<Stack><Subscript>60</Subscript><Superscript>+</Superscript></Stack> and Ga<Superscript>+</Superscript> projectiles

The ion bombardment-induced release of particles from a metal surface is investigated using energetic fullerene cluster ions as projectiles. The total sputter yield as well as partial yields of neutral and charged monomers and clusters leaving the surface are measured and compared with corresponding data obtained with atomic projectile ions of similar impact kinetic energy. It is found that all yields are enhanced by about one order of magnitude under bombardment with the C60+ cluster projectiles compared with Ga+ ions. In contrast, the electronic excitation processes determining the secondary ion formation probability are unaffected. The kinetic energy spectra of sputtered particles exhibit characteristic differences which reflect the largely different nature of the sputtering process for both types of projectiles. In particular, it is found that under C60+ impact (1) the energy spectrum of sputtered atoms peaks at significantly lower kinetic energies than for Ga+ bombardment and (2) the velocity spectra of monomers and dimers are virtually identical, a finding which is in pronounced contrast to all published data obtained for atomic projectiles. The experimental findings are in reasonable agreement with recent molecular dynamics simulations.     

On-line coupling of ion chromatography and atomic spectrometry for ultra trace analysis in high purity molybdenum- and tungsten-silicide

The well-established technique of on-line coupling ion chromatography and atomic spectrometry for ultra trace analysis in high purity molybdenum and tungsten is extended to include the silicides MoSi(x) and WSi(x). An additionally included matrix elimination step allows an almost interference-free trace analysis in the silicide matrices. Reproducibility and accuracy of the on-line method were checked by comparison with several other methods, such as isotope dilution, radiochemical neutron activation analysis, direct determination by atomic absorption analysis and not at least with glow discharge mass spectrometry. The results show the high potential of the on-line method for reaching detection limits in the pg g(-1) range, but they show also remaining problems with contamination and system calibration.     

How electrons guard the space: shape optimization with probability distribution criteria

Efficient formulas for computing the probabilities of finding exactly electrons in an arbitrarily chosen volume ³ for Hartree–Fock wavefunctions are presented. These formulas allow the use of shape optimization techniques, such as level set methods, for optimizing with respect to various criteria involving such probabilities. The criterion defined as the difference between the Hartree–Fock and the independent-particle model probabilities of finding electrons in stresses the quantum effects due to the Pauli principle. We have implemented a 2D level set method for optimizing this criterion in order to study spatial separation of electron pairs in linear molecules. The method is described and the illustrative example of the BH molecule is reported.Contribution to the Jacopo Tomasi Honorary Issue     

Chemical Reactions in the Manufacture of Waveguides for Long Distance Optical Data Transmission

One of the modern high technologies which has advanced enormously in the last few years is glass fiber technology. This is used in the manufacture of glass fibers for lighting purposes and for the optical transfer of analog and digital data with a high transfer density. The technical demands made on the glass fibers required for data transfer, the optical waveguides, are extremely high and are already fulfilled to a large extent by industry. At present about four million kilometers of fiber, worth ca. 800 million DM are produced worldwide (10% in the Federal Republic of Germany). Numerous chemical processes take place during the manufacture of optical waveguides. However, in contrast both to the high and constantly growing demands on the quality and to the increasing production volume of such fibers, little is in fact known about the reactions involved. The present article will attempt to develop a picture of the multifarious reactions occurring in the course of this technical process on the basis of literature data and our own studies.     

Direct optical emission spectroscopy of liquid analytes using an electrolyte as a cathode discharge source (ELCAD) integrated on a micro-fluidic chip

Atomic emission detection of metallic species in aqueous solutions has been performed using a miniaturised plasma created within a planar, glass micro-fluidic chip. Detection was achieved using an Electrolyte as a Cathode Discharge source (ELCAD) in which the sample solution itself is used as the cathode for the discharge. To realise the ELCAD technique within a micro-fluidic device, a parallel liquid-gas flow was set up in a micro-channel and a glow discharge ignited between the flowing liquid sample surface and a metal wire anode. The detection of copper and sodium was achieved, using atmospheric pressure air as a carrier gas, by observation of atomic emission lines of copper at 324 nm, 327 nm, 511 nm, 515 nm and 522 nm and an atomic emission line of sodium at 589 nm using a commercially available miniaturised spectrometer. A total electrical power of less than 70 mW was required to sustain the discharge. A semi-quantitative, absolute detection limit of 17 nmol s(-1) was obtained for sodium with a sample flow rate of 100 microL min(-1) and an integration time of 100 ms in air at atmospheric pressure. The volume required for such detection is approximately 170 nL. Further analysis was performed with an Echelle spectrometer using both argon and air as a carrier gas. The geometry and flow rates used demonstrate the feasibility of integrating such micro-plasmas into other micro-fluidic devices, such as miniaturised CE devices, as a method of detection. The potential for using such micro-plasmas within highly portable miniaturised systems and mu-TAS devices is presented and discussed.     

Determination of 1-vinyl-2-pyrrolidone in human serum by high-performance liquid chromatography

Summary A simple method is described which allows the quantification of 1-vinyl-2-pyrrolidone (NVP) in human serum. NVP is extracted from serum with diethylether and determined with HPLC/UV-detection. 1-Cyclohexyl-2-pyrrolidone serves as an internal standard. The detection limit is 0.1 mg/l. The method has shown that NVP can enter the organisms of workers occupationally exposed to this substance.     

Numerical analysis of electroosmotic flow in dense regular and random arrays of impermeable, nonconducting spheres

We present a numerical scheme for analyzing steady-state isothermal electroosmotic flow (EOF) in three-dimensional random porous media, involving solution of the coupled Poisson, Nernst-Planck, and Navier-Stokes equations. While traditional finite-difference methods were used to resolve the Poisson-Nernst-Planck problem, the (electro)hydrodynamics has been addressed with high efficiency using the lattice-Boltzmann method. The developed model allows simulation of electrokinetic transport under most general conditions, including arbitrary value and distribution of electrokinetic potential at the solid-liquid interface, electrolyte composition, and pore space morphology. The approach provides quantitative information on a spatial distribution of simulated velocities. This feature was utilized to characterize EOF fields in regular and random, confined and bulk packings of hard (i.e., impermeable, nonconducting) spheres. Important aspects of pore space morphology (sphere size distribution), surface heterogeneity (mismatch in electrokinetic potentials at confining wall and sphere surface), and fluid phase properties (electrical double layer thickness) were investigated with respect to their influence on the EOF dynamics over microscopic and macroscopic spatial domains. Most important is the observation of a generally nonuniform pore-level EOF velocity profile in the sphere packings (even in the thin double layer limit) which is caused by pore space morphology and which is in contrast to the pluglike velocity distribution in a single, straight capillary under the same conditions.