15N enrichment of ammonium, glutamine-amide and urea, measured via mass isotopomer analysis of hexamethylenetetramine.

Ammonium is an important intermediate of protein metabolism and is a key component of acid-base balance. Investigations of the metabolism of NH(4)(+) in vivo using isotopic techniques are difficult because of the low concentration of NH(4)(+) in biological fluids and because of frequent artifactual isotopic dilution of the enrichment of NH(4)(+) during the assay. A new gas chromatographic mass spectrometric method was designed to monitor the (15)N enrichment and concentration of NH(4)(+) in vivo. These are both calculated from the mass isotopomer distribution of hexamethylenetetramine (HMT) formed by reacting NH(4)(+) with formaldehyde. The enrichment of NH(4)(+) is amplified four times since the HMT molecule contains four atoms of nitrogen derived from NH(4)(+). This allows the measurement of low (15)N enrichment of NH(4)(+), down to 0.1%. (15)N enrichment of urea and of the amide N of L-glutamine are measured by enzymatic release of NH(4)(+) and conversion of the latter to HMT. These new techniques facilitate in vivo investigations of the metabolism of NH(4)(+) and related compounds.     

Liquid crystalline polymers at interfaces

Main chain liquid crystalline polymers (LCPs) at solid-nematic interfaces exhibit a variety of phase transition between distorted and undistorted states. In one case the transition results from the confinement of grafted chains immersed in a nematic solvent and subject to homeotropic anchoring. The general features of the transition are similar for long and for short chains. The detailed physics is different since long chains exhibit Gaussian, entropic elasticity while the elasticity of the short chain is due to their rigidity. As a result it is possible to weakly confine long chains without triggering a distortion while for short chains the nematic distortion occurs simultaneously with the buckling of the rod like LCPs. Related effects are found for uniformly adsorbed LCPs and for free, confined chains. Different scenarios are expected when homogeneous anchoring is imposed.     

Deformation of globular polysoaps: extension, confinement and extensional flow

A theoretical model of the extension and confinement of globular polysoaps predicts novel force laws. Polysoaps are polymers comprising of a flexible hydrophilic backbone incorporating, at intervals, amphiphilic monomers. The equilibrium configuration of long polysoaps, that form numerous spherical intrachain micelles, is a spherical globule of close packed micelles. The coupling of the deformation to the hierarchical self organization of the chain gives rise to a distinctive force law involving, for extension, two plateau regimes. When the chain is stretched by extensional flow the two regimes merge and the polysoap exhibits a single globule-stretch transition. Received 16 June 1998 and Received in final form 19 November 1998     

NMR on superfluid<Superscript>3</Superscript>He in aerogel

The transition to superfluidity of³He in high porosity (98.2%) acrogel has been observed by nuclear magnetic resonance techniques. The onset of the transition at all pressures above 13 bar is marked by a sharp increase in NMR frequency similar to that observed in bulk³He-A. This suggests that the aerogel/superfluid phase is highly homogeneous although both the transition temperature, T_c, and the amplitude of the order parameter are substantially suppressed. The acrogel strands are ≈ 50Å in diameter, much smaller than the superfluid coherence length. Consequently, we have attempted to interpret our observations as an impurity scattering problem. Based on our measurements of the magnetic field dependence of T_c it appears that both magnetic and potential scattering play important roles where the magnetic scattering can be associated with solid³He on the aerogel surface. This is determined by isotopic exchange with⁴He, a process which appears to stabilize a new superfluid state similar to the bulk B-phase.     

Domain Patterns in the Microwave-Induced Zero-Resistance State

It has been proposed that the microwave-induced “zero-resistance” phenomenon, observed in a GaAs two-dimensional electron system at low temperatures in moderate magnetic fields, results from a state with multiple domains, in which a large local electric field E(r) is oriented in different directions. We explore here the questions of what may determine the domain arrangement in a given sample, what do the domains look like in representative cases, and what may be the consequences of domain-wall localization on the macroscopic dc conductance. We consider both effects of sample boundaries and effects of disorder, in a simple model, which has a constant Hall conductivity, and is characterized by a Lyapunov functional.     

Hole-burning diffusion measurements in high magnetic field gradients

We describe methods for the measurement of translational diffusion in very large static magnetic field gradients by NMR. The techniques use a "hole-burning" sequence that, with the use of fringe field gradients of 42 T/m, can image diffusion along one dimension on a submicron scale. Two varieties of this method are demonstrated, including a particularly efficient mode called the "hole-comb," in which multiple diffusion times comprising an entire diffusive evolution can be measured within the span of a single detected slice. The advantages and disadvantages of these methods are discussed, as well as their potential for addressing non-Fickian diffusion, diffusion in restricted media, and spatially inhomogeneous diffusion.     

Electroluminescence (EL) from natural semiconducting (p-type) diamond

Microscopical examination in this work has shown the EL obtained from a semiconducting diamond using silver-paint electrodes to appear mainly at the negative electrode and only at very small points where the silver grains make contact with the crystal. Complications due to large variations in grain size and shape were eliminated by preparing silver-evaporated electrodes, with dimensions of the order of 1 μm. The EL brightness was found to increase with the decrease of the electrode size. An expression describing the dependence of the EL on the applied voltage and on the energy of the level to which excitation takes place was fitted to the experimental results. Detailed analysis of the EL suggested that electrons are raised by impact with holes to four discrete levels in the forbidden gap, probably from the level at 0.37 eV above the valence band present in these diamonds. The emission spectrum was found to show three peaks in the spectral range 3600–9000 Å, and indicated the existence of another peak beyond 9000 Å. All the emission bands seem to result from recombination at one common level, which should be the valence band itself or a level very close to it. Our emission spectrum fitted that given in the literature (ref. [13]) for cathodoluminescence of natural semiconducting diamond.