Diffractive scattering in the dual model

A method is suggested for calculating the elastic amplitude as the shadow of multiparticle processes. This does not require explicit formulae for the production amplitudes, but depends only on the following assumptions: (a) Regge behaviour, (b) semi-local duality, (c) exchange degeneracy. The system is multiperipheral in general structure but because of the assumption (a)-(c), it incorporates such features as the clustering of final particles and provides a proper treatment of quantum numbers, phases, and resonance spins. As a result, the unitarity sum separates automatically into two components corresponding respectively to pomeron and ordinary reggeon exchange, each of which is seen to have the correct qualitative dependence on the quantum numbers, the energy s, and the momentum transfer t. Quantitatively, the elastic amplitude is given in terms of a triple-Regge vertex, for which we suggest a simple parametization based on a detailed study of existing experiment and the Veneziano model. The method is then applied to calculate the elastic amplitudes for π^±p, K^±p and pp within the range 6 < s < 50 and 0 > t > ?0.5 GeV². Semi-quantitative agreement is obtained with experiment with essentially no free parameter. Although the investigation is restricted at present to elastic scattering as the shadow of only the non-diffractive component satisfying (a)-(c), the method is believed to apply also to other diffractive processes, and may be regarded as the first step in an iterative solution of the full unitarity equation.     

Robust likelihood inference for multivariate correlated count data

A parametric robust approach for analyzing correlated count data is introduced. This method enables one to construct an asymptotically valid likelihood for the regression parameter when knowledge about the joint distribution for data is scarce or not available. We use simulations and real data analysis to demonstrate the merit of the proposed robust likelihood method.     

Dynamic model for a defective production system with Poka-Yoke

This paper proposes a dynamic model for a defective production system with Poka-Yoke. Poka-Yoke is a Japanese phrase which means mistake-proofing. The technique of Poka-Yoke has been diversely applied in modern production systems. In this study, we evaluate the total cost of a defective production system with Poka-Yoke. We also use a practical case in automotive industry to verify the proposed model. The case study reveals that Poka-Yoke is a cost-effective mechanism that generates satisfactory return of a defective production system, the effect of which depends on the investment cost of Poka-Yoke.     

The laser vs. the lamp: Photochemistry of long-chained bis-dibenzylketones

A comparison of products formed during photolysis of 1,12-bis-[4-(2-oxo-3-phenylpropyl)phenyl]dodecane (1) reveals a difference in laser and lamp photolysis in that the use of a laser increases the yield of macrocyclic paracyclophane rings (2) by a factor of three.     

Front and back surface cw CO2-laser annealing of arsenic ion-implanted silicon

The annealing behavior of arsenic-implanted silicon under scanned cw CO₂-laser irradiation from front and back surfaces is investigated. Ellipsometry, Hall effect, Rutherford backscattering measurements and neutron activation analysis indicate an enhancement of annealing efficiency by laser irradiation from the back surface, which provides complete recovery of crystal damage, high substitutionality and electrical activation of implanted arsenic atoms without redistribution of concentration profile. The enhancement of annealing efficiency under back-surface irradiation is explained by the difference in laser reflection from the front and back surface of silicon wafers. No differences in the results are found for scanned and static annealing.     

Diastereoselective Friedel-Crafts alkylation of indoles with chiral alpha-phenyl benzylic cations. Asymmetric synthesis of anti-1,1,2-triarylalkanes

The reactions of chiral benzyl carbocations bearing alpha-phenyl substituents with N-sulfonylated indoles afford 1,1,2-triarylalkanes with anti-selectivities. This outcome is a reversal of facial diastereoselectivity relative to Bach's alpha-alkyl-bearing benzyl cations. The reactions are promoted by either a Br?nsted acid (TFA) or Lewis acid (BF3.OEt2), offering differential diastereoselectivities and reactivities. The electronic properties of both reacting partners strongly influence the reaction rates and the product diastereoselectivities and appear to operate under kinetic control. This chemistry provides an efficient access to sterically congested tetrasubstituted ethanes.     

An optical image stabilisation using a droplet manipulation on a liquid crystal and polymer composite film

ABSTRACT

We demonstrate an image system with an optical image stabilisation using a droplet manipulation on a liquid crystal (LC) and polymer composite film (LCPCF) to reduce motion blur while preserve image quality. Such an image system adopts a liquid lens on an LCPCF and the mechanism is on a basis of droplet movement on LCPCF whose position changes because electrically tunable orientations of LC molecules on the surface of LCPCF. The change of position of the liquid lens compensates the deviation of light as the image system is under a handshake vibration. As a result, the image system under handshake vibrations could keep a clear image. The operating principles are introduced, and the experiments are performed and discussed. The concept in this paper can also be extended to design other optical components for modulating direction of light.     

A computational study of organic polyradicals stabilized by chromium atoms

Density functional theory has been used to investigate the properties of organic high spin molecules. The M05/cc-pVDZ calculations predict a septet ground state for the 2,3,6,7,10,11-hexahydro-1,4,5,8,9,12-hexaoxocoronene-2,3,6,7,10,11-hexayl radical (coronene-6O). The computations show further that the formation of intermolecular carbon-carbon bonds yields a singlet ground state for the dimer rather than a possible tridectet state as expected from the monomer's multiplicity. A benzene molecule placed between coronene-6O molecules leads to the desired high-spin cluster, but the overall stability of the cluster is low. A chromium atom inserted between two peripheral C(6) rings of coronene-6O yields a sandwich structure with the expected tridectet ground state and a binding energy which is 15 times larger than the corresponding tridectet dimer stabilized by a benzene molecule. The presented DFT calculations suggest that a chromium atom can effectively link organic polyradicals to larger magnetic units.