The excitation and detection of multiple quantum transitions in systems of coupled spins offers, among other advantages, an increase in resolution over single quantum n.m.r. since the number of lines decreases as the order of the transition increases. This paper reviews the motivation for detecting multiple quantum transitions by a Fourier transform experiment and describes an experimental approach to high resolution multiple quantum spectra in dipolar systems along with results on some protonated liquid crystal systems. A simple operator formalism for the essential features of the time development is presented and some applications in progress are discussed.The energy level diagram of a system of coupled spins 1/2 in high field is shown schematically in fig. I. The eigenstates are grouped according to Zeeman quantum number mi with smaller differences in energy within a Zeeman manifold due to the couplings between spins and the chemical shifts. For any eigenstate 10 of the spin Hamiltonian H (in frequency units)The single quantum selection rule 1 of the low power c.w. experiment and the one dimensional Fourier transform experiment arises because
Couette and parallel plate viscometers are two commonly used flow geometries to characterize shear viscosity of concentrated suspensions. In Couette flow, it is well documented that prolonged shearing causes a decrease in the apparent viscosity of concentrated suspensions due to shear-induced particle migration from the annulus region to the stagnant region under the bob. In this study, the technique of nuclear magnetic resonance imaging (NMRI) was used to measure the evolution of suspension concentration profiles in Couette and parallel-plate flow devices upon shearing. Neutrally buoyant suspensions of nearly monodisperse, non-Brownian spherical particles at a volume fraction of 0.5 in a Newtonian fluid were used. The same flow cells and suspensions were also used in a rheometer to measure the changes in shear stress under identical experimental conditions such that a direct comparison can be made between the stress and concentration data. For Couette flow, the NMRI data correlated very well with the stress measurements and directly confirmed the Leighton–Acrivos [J. Fluid. Mech. 181, 415 (1987)] shear-induced migration theory. In torsional flow between parallel plates, no detectable change was found in particle concentration in the radial direction, but some decrease in the apparent viscosity was observed. These results provide some important clues for developing and evaluating more general descriptions of particle migration for nonrectilinear shear flows.
SynopsisSolutions of poly(vinyl alcohol) (PVA) and polysaccharide with sodium borate (SB) are investigated as a model system for associating polymers which exhibit shear-induced fluid structure and shear-thickening rheology. Certain combinations of PYA and SB concentrations are shown to result in fluids that exhibit a viscosity maximum followed by shear thinning as shear rate is increased. Stress saturation is often observed in the shear-thinning region. A significant hysteresis is also reported in which higher viscosities and lower shear rate for the viscosity maximum are observed in steady-state measurements made while decreasing shear rate in a stepwise manner. Boron nuclear magnetic resonance spectra are shown to be useful for elucidating the nature of the borate/hydroxyl-dyad complexes, including their stereoselectivity. Boron resonance peaks allow quantitative determination of the number of complexes. Dynamic mechanical properties are included, and a physical picture of network structure building and breaking during flow of associating polymers is discussed.
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