New aspects of micromachining and microlithography using 157-nm excimer laser radiation

The use of F₂ excimer laser sources, emitting at 157 nm, constitutes a new promising tool for scientific, industrial and lithography applications. The 157-nm laser emission enables high-resolution processes and the high photon energy offers the unique possiblity of photoionizing molecules in a single step. Therefore a lower fragmentation or thermal loading takes place. The 157-nm radiation will enable fundamental research and development for deep UV (DUV) high-resolution optical microlithography in the manufacturing of integrated circuits. This is the next step from the technology of ArF lasers at 193 nm. Furthermore, benefits are expected for key technologies requiring high-resolution processing and the micromachining of tough materials like Teflon or fused silica for micro-optics fabrication. Such applications require F₂ excimer laser sources with high performance, reliability and efficiency. The world of nanotechnology is just beginning to reveal its potential.     

CALCULATION OF DIFFUSION BARRIERS FOR HELIUM ATOM IN METALS

The diffusion barriers for the single helium atom in 3d transition metals are systematically studied by effective medium theory without any adjustable parameters. In the calculation, the relaxiation effects of lattice are taken into account. The comparison of our calculated results with the available experimental data and other theoretical values shows good agreement.     

Angular distributions of light projectile fragments in deep inelastic Pb + Em interactions at 160 A GeV

The nuclear emulsion was exposed at CERN by the lead projectile at 160 A GeV. The angles between any pair of fragments with Z = 2-4 have been measured in the emulsion plane for the events which did not contain heavy fragments. The constant characterizing the normal angle (J) distribution of the fragment momentum projection onto the emulsion plane with respect to initial projectile momentum p₀ is found to be C_J = (0.37 - 0.02) mrad. Corresponding value C₀ = (121 - 6) MeV/c of nucleon momentum distribution in the lead nucleus coincides with that expected from Fermi momentum distribution for this nucleus. The peak in the pair-angle distribution of double-charged fragments, ⁸Be M 2!, is presented for the region of small angles (<0.1 mrad). The fraction of !-particles coming from the decay of the ground state ⁸Be is found to be (13 - 2)% of their whole number.     

An analysis of maximum clique formulations and saturated linear dynamical network

Several formulations and methods used in solving an NP-hard discrete optimization problem, maximum clique, are considered in a dynamical system perspective proposing continuous methods to the problem. A compact form for a saturated linear dynamical network, recently developed for obtaining approximations to maximum clique, is given so its relation to the classical gradient projection method of constrained optimization becomes more visible. Using this form, gradient-like dynamical systems as continuous methods for finding the maximum clique are discussed. To show the one to one correspondence between the stable equilibria of the saturated linear dynamical network and the minima of objective function related to the optimization problem, La Salle's invariance principle has been extended to the systems with a discontinuous right-hand side. In order to show the efficiency of the continuous methods simulation results are given comparing saturated the linear dynamical network, the continuous Hopfield network, the cellular neural networks and relaxation labelling networks. It is concluded that the quadratic programming formulation of the maximum clique problem provides a framework suitable to be incorporated with the continuous relaxation of binary optimization variables and hence allowing the use of gradient-like continuous systems which have been observed to be quite efficient for minimizing quadratic costs.     

A bifurcated waveguide problem

We consider the diffraction of the dominant mode in a parallel-plate waveguide with hard boundaries which is incident on a centered soft-hard half-plane. By using the Fourier transform technique in conjunction with the Mode Matching method, the related boundary value problem is formulated as a modified Wiener-Hopf equation. The solution of the latter, which contains infinitely many constants, is found by solving numerically an infinite set of linear algebraic equations.     

On the Chemical and Structural Rearrange of Hg-organyltellurolate Clusters: Synthesis, X-ray Characterization, TGA and Raman Evaluation of [(PhTe)6(Ph3P)2Hg5Cl4]?·?2THF and [(PhTe)8Hg6Py2Cl4]?·?Py (Py = pyridine)

(PhTe)₂Hg reacts with HgCl₂ and triphenylphosphine to give the clusters [(PhTe)₆(Ph₃P)₂Hg₅Cl₄] · 2THF (1) and [(PhTe)₈Hg₆Py₂Cl₄] · Py (Py = pyridine) (2). In 1 each tellurium atom connects two Hg atoms, with Hg–Te distances around 2.75 Å. Phosphorus atoms of the triphenylphosphine groups complete the tetrahedral coordination of the Hg1 atoms. The second set of Hg atoms (Hg2) is also coordinated to chlorine atoms. The three-dimensional assembling of 1 encloses circular channels with medium diameter of 12.5 Å. The cluster 2 results from substitution of the oxidized triphenylphosphine ligands of 1 by one molecule of Hg(PhTe)₂ in the course of the synthetic procedures. The alternated Te–Hg bonds of 2 close a 12-membered ring with two inverted 4-membered rings in the middle. Thermogravimetrical evaluations and Raman scattering lines of 1 and 2 are also discussed.

Effect of methanol dilution on H-ZSM-5 zeolite deactivation in the process of light olefin formation

Conversion of methanol in the presence of H₂O, O₂, H₂, CO, CO₂ and He was studied at 733 K on H-ZSM-5 zeolite. The effect of diluent on the selectivity to light olefins and resistance to coking of H-ZSM-5 were observed. Among the diluents studied only water exerts a promoting effect on prolonged activity of the catalyst. Some explanations of the deactivation process are given.

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H₂O, O₂, H₂, CO, CO₂ He H-ZSM-5 733K. H-ZSM-5. . .

     

The significance of Kekulé structures for the stability of aromatic systems—II

Dihydroheptazethrene (V) and 1:14,11:12-dibenzo-5,7-dihydro-pentacene (VI) were synthesized. The former gave heptazethrene (VII) on dehydrogenation, whilst the latter polymerized immediately. This difference is explained by the fact that heptazethrene (VII) can be formulated with a Kekulé structure and the dehydrogenation product of VI cannot. Heptazethrene is a basis hydrocarbon and is closely related to dibenzoheptazethrene (VIII). Heptazethrenequinone (II) is a true quinone giving a blue vat, whilst the isomer (IV) is a diketone and does not give a vat.     

Al2O3-supported Fe?Ni catalysts for CO hydrogenation, I. Catalytic properties

CO conversion to hydrocarbons at various reaction temperatures and atmospheric pressure has been investigated on alumina-supported Fe, Ni and Fe–Ni catalysts. Maxima of activity and selectivity were obtained in hydrocarbon formation as a function of Fe content in the samples, which corresponds to a certain stoichiometry of metallic components.