Short-range order and F ion diffusion inside the Pb1 − xAlxF2 + x solid solution Part II: Al NMR investigation and proposal of clustering process

A ²⁷Al nuclear magnetic resonance (NMR) investigation at room temperature of the Pb_{1 − x}Al_xF_{2 + x} (0 ≤ x ≤ 0.12) solid solution and of the ordered Pb₉Al₂F₂₄ phase is carried out. Two different types of aluminium ions are identified and their ratio is determined as a function of x. A clustering process based on the formation of column clusters, more and more extended when x increases, is proposed on the basis of results issued from the ¹⁹F (Part I) and ²⁷Al NMR investigations.     

On the relation between protonium level shifts and nucleon-antinucleon scattering amplitudes

We study the Coulomb and threshold corrections to the low-energy scattering parameters for the proton-antiproton system, with numerical examples based on current optical models. Some commonly used expressions are shown to be inconsistent with our results. We check that the Trueman formula is valid for the level shifts of protonium, provided one takes properly into account the Coulomb corrections to the scattering lengths and volumes.     

A method for investigating the orientational behaviour of fibrous particles in gaseous flow

A method is described by which the angular orientation distribution of fibrous particles carried in a gaseous stream may be investigated. The method is based upon the interpretation of the spatial intensity distribution or scattering profile of laser light scattered by individual fibres. The scattering instrument used to capture the profiles is described, and the mathematical computation required to ascertain the orientation of each particle at the measurement point is detailed. Illustrative results are given for a study of airborne micromachined silicon particles of 12 μm length and 1.0 μm by 1.5 μm cross-section. The method is currently being employed by the authors to investigate ways of improving the orientation control over nonspherical particles in systems such as aerodynamic particle sizers and particle shape classifiers, since lack of particle orientation control is known to adversely affect the measurement accuracy of both these types of instrument.     

Orientation and relaxation of polymer–clay solutions studied by rheology and small-angle neutron scattering

The influence of shear on viscoelastic solutions of poly(ethylene oxide) (PEO) and clay [montmorillonite, i.e., Cloisite NA+ (CNA)] was investigated with rheology and small-angle neutron scattering (SANS). The steady-state viscosity and SANS were used to measure the shear-induced orientation and relaxation of the polymer and clay platelets. Anisotropic scattering patterns developed at much lower shear rates than in pure clay solutions. The scattering anisotropy saturated at low shear rates, and the CNA clay platelets aligned with the flow, with the surface normal parallel to the gradient direction. The cessation of shear led to partial and slow randomization of the CNA platelets, whereas extremely fast relaxation was observed for laponite (LRD) platelets. These PEO–CNA networklike solutions were compared with previously reported PEO–LRD networks, and the differences and similarities, with respect to the shear orientation, relaxation, and polymer–clay interactions, were examined. © 2004 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 42: 3102–3112, 2004     

Potential-dependent structure of the interfacial water on the gold electrode

Doubly tunable sum frequency generation (SFG) spectra demonstrate that the water molecules at gold/electrolyte interface change their orientation with applied potential. At negative potentials, water molecules in the double layer align with their oxygen atom pointing to the solution. As potential became positive to be close to the potential of zero charge (PZC), the SFG signal decreased, suggesting the OH groups of the water molecule are either in random orientation or parallel to the electrode. As potential became more positive than the PZC, the SFG signal increased again with the oxygen-up orientation as same as in the negative potential region, indicating that water molecules interact with the adsorbed sulfate anions. The peak position of the SFG spectra indicates a relatively disordered state of water molecules at the gold electrode surface, in contrast to the previously observed ice-like structure of water at electrolyte/oxide interfaces.