Polymer Induced Drag Reduction in a Turbulent Pipe Flow Subjected to a Coriolis Force

The skin friction factor f in a turbulent wall-bounded flow can be greatly reduced by using polymer solutions. In this paper we discuss experimental results on the effect of the Coriolis force on turbulent drag reduction. To study this, a horizontal smooth-walled pipe with internal diameter 25?mm is placed on a horizontal table rotating about its vertical axis. The rotation is made non-dimensional with friction velocity and pipe diameter, to form the Rotation number Ro. For a range of bulk Rotation number (Ro _b ) between 0 and 0.6 for two different Reynolds numbers (Re _b = 15 & 30 × 10³), the pressure drop is measured, from which the average friction factor f is obtained. Additionally the effect of four different polymer concentrations has been investigated. The single-phase results show that the friction factor increases monotonic but gradual with Rotation. With polymer additives a drag reduction is found that increases with concentration, but which is not affected by the rotation.     

Reversed phase HPLC of different membrane-bound variant surface glycoprotein preparations from Trypanosoma brucei brucei

The chromatographic behaviour of the membrane-attached variant surface glycoprotein (mfVSG) of bloodstream forms of Trypanosoma brucei brucei AnTat 1.1 A preparations were studied by reversed phase high performance liquid chromatography (RP-HPLC). Among the different preparation procedures used, only the trifluoroacetic acid extraction gave a mfVSG preparation which was eluted from the RP-HPLC column. As well as for the soluble variant surface glycoprotein (sVSG) it was found that different mfVSG forms were eluted at different organic solvent concentrations from the RP-HPLC column. In addition, in preliminary studies, we have attempted to characterize the factors responsible for the trypanosome surface coat assembly. Using chromatographic techniques (RP-HPLC and thin layer chromatography), the results suggest a close relationship between the content of lipid-containing species and the heterogeneity of mfVSG preparation.     

Spin-momentum correlations in quasielastic electron scattering from deuterium

The spin-momentum correlation parameter A(V)(ed) was measured for the 2H-->(e-->,e'p)n reaction for missing momenta up to 350 MeV/c at Q2 = 0.21 (GeV/c)(2) for quasielastic scattering of polarized electrons from vector-polarized deuterium. The data give detailed information about the deuteron spin structure and are in good agreement with the results of microscopic calculations based on realistic nucleon-nucleon potentials and including various spin-dependent reaction mechanism effects. The experiment reveals in a most direct manner the effects of the D state in the deuteron ground-state wave function and shows the importance of isobar configurations for this reaction.     

Selective liquid-phase semihydrogenation of functionalized acetylenes and propargylic alcohols with silica-supported bimetallic palladium-copper catalysts

Silica-supported, bimetallic palladium-copper catalysts were prepared in solution under mild conditions by reacting lithium di(4-tolyl)cuprate with palladium acetate in the presence of silica particles. Small bimetallic palladium-copper particles were deposited on the silica surface as confirmed with TEM-EDAX and EXAFS. The new material has been applied as catalyst in the liquid-phase semihydrogenation of mono- and disubstituted alkynes and showed high selectivity toward the cis-alkenes. The influence of addition of quinoline or potassium hydroxide to the semihydrogenation reaction mixture and the effects of exposure of the catalyst to air before use have been investigated.     

Intermediate-range potential and the 1S0neutron-proton transition matrix

The half-shell transition matrix t(p, k) for the singlet s-wave neutron-proton interaction has been studied for a class of partly non-local potentials. The potentials have been generated from the experimental phase shifts by using inverse scattering theory. The non-uniqueness of the inversion solution has been exploited to construct potentials with different short-range behaviour. It is shown that the intermediate-range potential essentially determines t(p, k) for momenta p and k both less than 2fm^?. Different short-range behaviour is reflected in t(p, k) for larger momenta. The unknown high-energy phase shifts imply, however, comparable variations in that region even if the on-shell momentum k is small. The implications for nuclear structure calculations are discussed.     

Experiments with longitudinally polarized electrons in a storage ring using a siberian snake

We report on first measurements with polarized electrons stored in a medium-energy ring and with a polarized internal target. Polarized electrons were injected at 442 MeV (653 MeV), and a partial (full) Siberian snake was employed to preserve the polarization. Longitudinal polarization at the interaction point and polarization lifetime of the stored electrons were determined with laser backscattering. Spin observables were measured for electrodisintegration of polarized 3He, with simultaneous detection of scattered electrons, protons, neutrons, deuterons, and 3He nuclei, over a large phase space.     

Temperature dependence of the penetration depth in Sr2RuO4: evidence for nodes in the gap function

We report measurements of the magnetic penetration depth in single crystals of Sr2RuO4 down to 0.04 K using a tunnel-diode based, self-inductive technique. We observe a power law temperature dependence below 0.8 K, with no sign of a second phase transition nor of a crossover predicted for a multiband superconductor. A power law dependence suggests that the gap function has nodes, inconsistent with candidate p-wave states. We argue that nonlocal effects, rather than impurity scattering, can explain the observed T2 dependence instead of the T-linear behavior expected for line nodes.     

Interfacial tension between a liquid crystalline polyesteramide and polypropylene obtained by dielectric spectroscopy

Dielectric spectroscopy is an unexplored technique in the elucidation of the morphology of polymer blends. Especially the appearance of interfacial polarization can reveal important information about the microstructure of a polymer blend. A model system of liquid crystalline polymer fibers lined up in a thermoplastic matrix was investigated. After heating above the melting temperature of both phases, the fibers developed distortions which grew with time. Dielectric spectroscopy was used to follow the change in shape of the distorted fibers. The use of only two frequencies made it possible to increase the number of relevant data points in the initial stages of the fiber breakup process. From these measurements it was possible to calculate the growth rate and hence the interfacial tension between the two polymers. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 815–825, 1998     

The onset of coulomb explosions in polyatomic molecules

With the development of high intensity femtosecond lasers, the ionisation and dissociation dynamics of molecules has become an area of considerable interest. Using the technique of femtosecond laser mass spectrometry (FLMS), the molecules carbon disulphide, pyrimidine, toluene, cyclohexanone and benzaldehyde are studied with pulse widths of 50 fs in the near infrared (IR) wavelength region (790 nm). Results are presented and contrasted for laser beam intensities around 10(15) and 10(16) W cm(-2). For the lower intensities, the mass spectra yield dominant singly charged parent ions. Additionally, the appearance of doubly charged parent ions is evident for carbon disulphide, toluene and benzaldehyde with envelopes of doubly charged satellite species existing in these local regions. Carbon disulphide also reveals a small triply charged component. Such atomic-like features are thought to be a strong fingerprint of FLMS at these intensities. However, upon increasing the laser intensity to approximately 10(16) W cm(-2), parent ion dominance decreases and the appearance of multiply charged atomic species occurs, particularly carbon. This phenomenon has been attributed to Coulomb explosions in which the fast absorption of many photons may produce transient highly ionised parent species which can subsequently blow apart. Copyright 1999 John Wiley & Sons, Ltd.     

Uniform molecular analysis using femtosecond laser mass spectrometry

The potential of femtosecond laser time-of-flight mass spectrometry (FLMS) for uniform quantitative analysis of molecules has been investigated. Various samples of molecular gases and vapours have been studied, using ultra-fast ( approximately 50 fs) laser pulses with very high intensity (up to 1.6 x 10(16) Wcm(-2)) for non-resonant multiphoton ionisation/tunnel ionisation. Some of these molecules have high ionisation potentials, requiring up to ten photons for non-resonant ionisation. The relative sensitivity factors (RSF) have been determined as a function of the laser intensity and it has been demonstrated that for molecules with very different masses and ionisation potentials, uniform ionisation has been achieved at the highest laser intensities. Quantitative laser mass spectrometry of molecules is therefore a distinct possibility. Copyright 1999 John Wiley & Sons, Ltd.