N\bar N annihilation into two body channels

A simple model is constructed forN¯N annihilations into two non-strange mesons. Determining the ratio of isospin one to isospin zero annihilation by experimental information we predict the branching ratios for these channels. The agreement with experiment is surprisingly good.     

Magnetic resonance imaging and pulsed Doppler sonography of poststenotic jets: Correlation between signal void and flow velocity distribution

To correlate the appearance of poststenotic jets on gradient echo images with features of localized Doppler spectra of the jets, we studied an in vitro model of steady flow-through stenoses of 86, 96, and 99% area reduction. As fluids, water and a 40% glycerol solution in water were used. MRI was performed with a 1.5 T whole body imager and gradient echo images were obtained in planes parallel to the direction of flow. Doppler spectra were acquired separately from the MR measurements at 1 cm intervals for a distance of 10 cm downstream from the stenosis. Poststenotic signal void was observed for water and for the 40% glycerol solution only if the mean velocity within the stenosis exceeded a limit of 50–60 cm/sec. On the MR images, the jets could be divided into two segments: A proximal jet segment of uniform width equal to the diameter of the stenosis, followed by a distal jet segment which was characterized by broadening and then dissipating signal void. Except for the 99% stenosis, a high signal intensity core was present within the proximal jet segment. In the proximal jet segment, the Doppler measurements showed a low temporal fluctuation of the maximal flow velocity and only little flow opposite to the main flow direction. In the distal jet segment, the velocity fluctuation and the intensity of reverse flow increased sharply. The high signal intensity core of the jet was associated with a poststenotic zone of constant maximal flow velocity. The results demonstrate a close relationship between characteristic features of poststenotic jets in MRI and pulsed Doppler sonography.     

Quantum size effects in the attractive hubbard model

We investigate superconducting pair correlations in the attractive Hubbard model on a finite square lattice. Our aim is to understand the pronounced size dependence which they display in the weak and intermediate coupling regimes. These size effects originate from the electronic shell structure of finite systems and severely complicate a reliable extrapolation of numerical simulation data from small systems to the thermodynamic limit. To analyze the size effects in detail, we use the BCS approximation, as well as a particle number conserving modification of it and compare the results with those of quantum Monte Carlo simulations. As an application, we explore the possibility of reducing the shell effects in simulation data by changing the shape of the system and the imposed boundary conditions and by making use of the size dependence of corresponding BCS data.     

某些查耳酮化合物的发光

本文叙述了两个同质查耳酮系列的合成.一个带有查耳酮中心链(系列Ⅰ),另一个是系列Ⅰ的酯类(系列Ⅱ).研究了每个系列中三种化合物的发光,发现两个系列的所有化合物都能见到发光.系列Ⅰ中的化合物在峰值为360nm处可见到发光,而系Ⅱ列中的化合物未能观测到这一波长的发光.然而,在峰值为470nm处两者均可见到发光.得出的结论是,消除非键电子微扰作用的氢键是系列Ⅰ中的化合物在360nm处出现发光的原因.     

On the diameter and radius of randon subgraphs of the cube

The n-dimensional cube Qⁿ is the graph whose vertices are the subsets of {1,…n}, with two vertices adjacent if and only if their symmetric difference is a singleton. Clearly Qⁿ has diameter and radious n. Write M = n2^n-1 = e(Qⁿ) for the size of Qⁿ. Let Q = (Q_t)_o^M be a random Qⁿ-process. Thus Q^t is a spanning subgraph of Qⁿ of size t, and Q_t is obtained from Q_t–1 by the random addition of an edge of Qⁿ not in Q_t–1, Let t^(k) = τ(Q;δ?k) be the hitting time of the property of having minimal degree at least k. We show that the diameter d_t = diam (Q_t) of Q_t in almost every Q? behaves as follows: d_t starts infinite and is first finite at time t⁽¹⁾, it equals n + 1 for t⁽¹⁾ ? t⁽²⁾ and d_t, = n for t ? t⁽²⁾. We also show that the radius of Q_t, is first finite for t = t⁽¹⁾, when it assumes the value n. These results are deduced from detailed theorems concerning the diameter and radius of the almost surely unique largest component of Q_t, for t = Ω(M). © 1994 John Wiley & Sons, Inc.     

The Post-Hopf-Bifurcation Response of a Loosely Supported Cylinder in an Array Subjected to Cross-Flow. Part II: Theoretical Model and Comparison with Experiments

A nonlinear quasi-steady model for the analysis of the dynamics of a loosely supported cylinder, which takes into account position-dependent nonlinear fluid forces as well as nonuniform flow, is formulated. The model includes an approximation for the equivalent viscous damping associated with energy dissipation on impact at the support. The nonlinear model shows reasonably good agreement with experiments, in predicting the observed bifurcations in the cylinder response. Comparison criteria include the standard orbital plots, time traces and response spectra. A borderline chaotic response is found to be predominant over the test velocity range. In this chaotic regime, the theoretical results were verified via attractor fractal-dimension calculations and saddle orbit distributions; theoretical values of these invariant measures compare reasonably well with their experimental counterparts. Two mechanisms leading to chaos have been identified for this system. The first is a switching mechanism , at the onset of impacting. The second, and more prevalent, is the type I intermittency route to chaos.     

Intramolecular hemiacetals. The acid-base-catalyzed ring-chain interconversion of 2-substituted 2-hydroxy-4,4-dimethylmorpholinium cations in aqueous solution.

The ring-chain tautomerism in aqueous solution of some aryl-substituted morpholinium salts (bromides), has been studied and equilibrium constants are reported. In the crystals the substrates exist entirely in their cyclic forms as hemiacetals, but in aqueous solution NMR measurements reveal that an equilibrium is established between the cyclic (hemiacetal) and the noncyclic (ketone) form, the degree of ring-opening being more pronounced with electron-donating aryl substituents at the carbonyl carbon. The kinetics of the ring-chain interconversion in water has been investigated spectrophotometrically by a 'pH jump' stopped-flow technique. General base catalysis is observed with a Br?nsted beta value apparently independent of substituent and equal to 0.60. The Hammett rho values for various base catalysts are close to those for very similar intermolecular reactions involving hemiacetal breakdown, leading to the suggestion of a 'normal' class n mechanism for base catalysis. For acid catalysis, however, a quite different situation is encountered, since no general acid but only (weak) catalysis by the hydronium ion can be detected. We believe this deviation from 'normal' general acid catalysis is caused by an electrostatic interaction, and we suggest that it might result from a change in the usual class e mechanism for general acid catalysis by a situation in which rate-limiting concerted proton transfer is replaced by rate-limiting preprotonation. This is supported by the observed drastic change in Hammett rho value for catalysis by the hydronium ion, compared with the 'normal' case. An interesting case is encountered for the 4-aminophenyl-substituted substrate, in which the amino group becomes protonated in acid solution, thus representing a new substituent. Despite this complication, the various equilibrium and rate constants may also be evaluated experimentally for this substrate.     

Gas chromatographic-mass spectrometric detection of trace amounts of organic compounds in the intravenous solution Infusio Darrowi.

A gas chromatographic-mass spectrometric procedure was employed to confirm the presence of trace amounts of organic compounds in the intravenous solution Infusio Darrowi. Organic contaminants in the solution analysed were concentrated by microextraction with n-pentane. The main compounds detected were 2,6-di-tert.-butyl-4-methylphenol, 2,6-di-tert.-butyl-4-ethylphenol, 2,6-di-tert.-butyl-4-methoxyphenol, benzothiazole, isomeric C9 alkyl phenols and di(n-butyl) phthalate. These impurities were leached from rubber stoppers during their sterilization into the intravenous solution at levels ranging ca. from 5 x 10(-6) to 5 x 10(-8) g/l.