Remarks on the exoticU-meson

In expectation of imminent result from the new hyperon beam experiment at CERN concerning the exoticU-meson at 3.1 GeV, we propose a detailed program of experimental tests to check the suggestion thatU is a \(qq\bar q\bar q\) “M-diquonium” state. Apart from some very characteristic decay modes, theU is expected to occur together with several analogous states with various quantum numbers to which it is intimately related.     

Random phase-coded multiplexing of hologram volumes using ground glass

We apply an encoding method, random phase-coded multiplexing, to volume hologram multiplexing and demonstrate the recording of 100 holograms in LiNbO₃: 0.01% Fe. A theory is developed to interpret the noise generated by this method, and a computer simulation is provided for direct comparison.     

Parallel processing of remotely sensed data: Application to the ATSR-2 instrument

Massively parallel computational paradigms can mitigate many issues associated with the analysis of large and complex remotely sensed data sets. Recently, the Beowulf cluster has emerged as the most attractive, massively parallel architecture due to its low cost and high performance. Whereas most Beowulf designs have emphasized numerical modeling applications, the Parallel Image Processing Environment (PIPE) specifically addresses the unique requirements of remote sensing applications. Automated, parallelization of user-defined analyses is fully supported. A neural network application, applied to Along Track Scanning Radiometer-2 (ATSR-2) data shows the advantages and performance characteristics of PIPE.     

Fabrication of three-dimensional crystalline microstructures by selective ion implantation and chemical etching

We present a new fabrication technique to produce three-dimensional (3D) microstructures on crystalline substrate using selective ion implantation and chemical etching. Localized lattice-damage layers at the specified depth beneath the substrate surface are formed by selective ion implantation. After etching out the partial surface regions and the buried lattice-damage layers by chemical etching, the 3D crystalline microstructures are produced. This technique is demonstrated on LiNbO₃ crystal to produce undercutting and free-standing microstructures, including microwire, microring, and microdisk. The measurement results of micro-Raman spectra show that the used fabrication process does not affect the original crystalline structure. The features of this technique include smooth structure surface, large undercutting range, and auto-etching stop. By using multiple implantations or repeating the proposed process several times, versatile 3D crystalline microstructures can be produced.     

Simultaneous determination of ampicillin, cefoperazone, and sulbactam in pharmaceutical formulations by HPLC with beta-cyclodextrin stationary phase

An accurate and reproducible method for the simultaneous determination of ampicillin (AMP), sulbactam (SUL), and cefoperazone (CFP) in pharmaceutical formulations by using HPLC with beta-CD stationary phase was developed. It involved the use of the added tetraethylammonium acetate (TEAA) reagent, pH, and methanol as the significant parameters to find the optimum separation condition. A high resolution and selectivity of analytes was obtained by running the mobile phase in methanol-5 mM TEAA buffer = 35:65 (v/v, pH 4.5) at 280 nm. The mean recoveries ranged from 96.6 to 103.3% for AMP in the synthetic mixture, 97.6 to 103.0% for SUL, and 97.0 to 104.0% for CFP. The low LOD (<1.8 microg/mL) and low CV (<0.9%) assured that this method was sensitive and reproducible. The assay of analytes in commercial products exhibited that it was convenient and reproducible for routine analyses of these components in sterilized H(2)O, saline, or 5% dextrose injection solutions.     

An efficient preparation of vinamidinium hexafluorophosphate salts

Substituted acetic acids or acetyl chlorides react with phosphorus oxychloride in DMF to yield the vinamidinium salts 3a-j in moderate to excellent recrystallized yields (28-90%). The cations are conveniently isolated as their hexafluorophosphate salts, which are easily handled nonhygroscopic solids. The nitro compound 3l is prepared in 91% yield by nitration of the parent vinamidinium 3k. The X-ray crystal structure is reported for the 2-phenyl isomer 3e and displays minimal overlap of the two pi-systems.     

Reactions of Diethyl [(3-Bromomethyl-2-Thienyl)-Methylene]Propanedioate with Hydrazines: Syntheses of Dihydropyridazines,Pyridazines and O-Dimethylaminomethylarenecarbonitriles

Facile syntheses of dihydropyridazines, pyridazines, and o-dimethylaminomethylarenecarbonitriles have been achieved by the retro-malonate addition reaction. Bromoalkylidenemalonates 1,7, and 10 were treated with hydrazine to give dihydropyridazines 4, 8, and 11 in quantitative yields. DDQ or air oxidation of 4, 8, and 11 gave pyridazines 5, 9, and 12, Alternatively, treatment of 1, 7, and 10 with 1,1-dimethylhydrazine afforded o-dimethylaminomethylarenecarbonitriles 6,13, and 14 in good yields.     

Structure and dynamics of carbon black‐filled elastomers

The linear and nonlinear melt viscoelastic properties for a series of carbon black‐filled polymer composites were studied. Complementary tapping‐mode atomic force microscopy (AFM) studies were used to examine the dispersion and structural correlations of the filler particles in these composites. The low‐frequency dependence of the linear viscoelastic moduli gradually changes from liquidlike behavior for the unfilled polymer to pseudosolid character for composites with more than 9 vol % carbon black filler. The plateau modulus, inferred from the linear viscoelastic response, exhibits a somewhat discontinuous change at about 9 vol % filler. On the basis of the linear viscoelastic response, we postulate that the carbon black filler forms a continuous percolated network structure beyond 9 vol % filler, considerably lower than that expected from theoretical calculations for overlapping spheres and ellipsoids. We suggest that the lower threshold for percolation is due to the polymer mediation of the filler structure, resulting from the low functionality of the polymer and, consequently, few strong polymer–filler interactions, allowing for long loops and tails that can either bridge filler particles or entangle with one another. Furthermore, the strain amplitude for the transition from linear behavior to nonlinear behavior of the modulus for the composites with greater than 9 vol % filler is independent of frequency, and this critical strain amplitude decreases with increasing filler concentration. Complementary AFM measurements suggest a well‐dispersed carbon black structure with the nearest neighbor distance showing a discontinuous decrease at about 9 vol % filler, again consistent with the formation of a filler network structure beyond 9 vol % carbon black. © 2000 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 39: 256–275, 2001     

On the strategy of supply chain collaboration based on dynamic inventory target level management: A theory of constraint perspective

After the financial tsunami in 2008, how to adjust the target inventory level dynamically and instantly in order to reduce the risk that an enterprise encountered in a rapid demand changing market has become a crucial issue in the field of supply chain management. This paper explores the strategies of supply chain collaboration by utilizing theory of constraint to achieve the goal of adjusting the target inventory level dynamically. Three time-series-data-mining techniques – Sequential Probability Ratio Test (SPRT), CUSUM chart and Auto-regression Test (AR(1)) are used to detect the timing of market demand change. The results are used to adjust the target inventory level. Simulation techniques are used to explore the relative efficiency of the demand-change detection for the three methods. The techniques are also used to explore the effectiveness of various inventory management strategies on inventory performance based on the three demand change detection methods.     

Parallel synthesis of natural product-like polyhydroxylated pyrrolidine and piperidine alkaloids

The preparation of natural product-like polyhydroxylated pyrrolidine and piperidine alkaloids using a combination of solid– and solution-phase organic synthesis is described. The key intermediates, enantiopure five- or six-membered tri-O-benzyl cyclic nitrones, were efficiently prepared on solid support from accessible chiral furanosides and pyranosides, respectively. The substituent diversity was achieved by a diastereoselective addition of a variety of Grignard reagents to the cyclic nitrones in solution-phase synthesis. All reaction steps and work-up procedures were modified to allow the use of automated equipment. A 36-membered demonstration library with three diversity elements (core, configuration, and substituent) was prepared in good yield and purity.