Neutron scattering variation

Two physically reasonable but quite different models have been used to describe the internal motions of lipid molecules observed by neutron scattering. In the first the protons are assumed to undergo diffusion in a sphere [63]. The radius of the sphere is allowed to be different for different protons. Although the results do not seem to be sensitive to the details of the variation in the sphere radii, it is necessary to have a range of sphere volumes, with the largest volume for methylene groups near the ends of the hydrocarbon chains in the middle of the bilayer and the smallest for the methylenes at the tops of the chains, closest to the bilayer surface. This is consistent with the behavior of the carbon-deuterium order parameters,. S cd, measured by deuterium NMR ... 

Figure 2 Variations in the neutron scattering amplitude or scattering length as a function of the atomic weight. The irregularities arise from the superposition of resonance scattering on a slowly increasing potential scattering. For comparison the scattering amplitudes for X rays under two different conditions are shown. Unlike neutrons, the X-ray case exhibits a monotonic increase as a function of atomic weight.

The Debye temperatures of stages two and one were determined by inelastic neutron scattering measurements [33], The total entropy variation using equation 8 is in the order of about 2 J/(mol.K). Although smaller in value, such variation accounts for 10-15% of the total entropy and should not be neglected. We are currently carrying on calculations of the vibrational entropy from the phonon density of states in LixC6 phases. 

Robinson BH, Toprakcioglu C, Dore JC, Chieux P (1984) Small-Angle Neutron-Scattering Study of Microemulsions Stabilized by Aerosol-Ot.l. Solvent and Concentration Variation. J Chem Soc Faraday Trans 1 80 13-27... 

PAD (perturbed angular distribution) is a variation of PAC with nuclear excitation by a particle beam from an accelerator. QMS is quasielastic MdBbauer-spectroscopy, QNS is quasielastic neutron spectroscopy. For MOBbauer spectroscopy (MS), perturbed angular correlation (PAC), and /J-nuclear magnetic resonance (/3-NMR), the accessible SE jump frequencies are determined by the life time (rN) of the nuclear states involved in the spectroscopic process. Since NMR is a resonance method, the resonance frequency of the experiment sets the time window. With neutron scattering, the time window is determined by the possible energy resolution of the spectrometer as explained later. 

In PB networks, the variation of the line shape as a function of the applied stress was interpreted in terms of a chain length distribution. Shorter chains may be more oriented than longer ones, at a given elongation [18], which may lead to a non-affine behaviour at the chain scale. The question of the spatial scale to which the deformation is affinely transmitted, has been investigated intensively by small angle neutron scattering [64]. However, it may happen as well that the chain portions close to junction points are more oriented (have a more restricted mobility) than those in the middle of the chains [19]. 

Now, we may evaluate the surface reconstruction generated by the suppression of a few kilobars of stress along the d axis, using the deformation coefficients under hydrostatic pressure. The authors of Ref. 136 have determined, in neutron-scattering experiments, the variation of the crystallographic parameters of anthracene ... 

Using this local moment model, and using band theory or its variations, a number of workers have been able to formulate expressions which represent the measured magnetic data reasonably well, at least for the case where well-localized moments are developed on the solute atoms (II, 18). However, considerably more data has become available on other properties of dilute alloys, including data on resistivity and specific heat, neutron scattering, various magnetic resonance experiments, Moss-bauer measurements, Kondo effect, and the like. Measurements have been extended also to alloys of many other systems besides those involving the platinum metals. 

Microemulsions consist of oil, water and an oil-water interfacial Him. DLS and SLS have been used to determine the translational diffusion coefficient and the interaction potential of microemulsions [45—47). The thickness of the inter-facial film and its curvature were measured by the contrast variation method in neutron scattering [48,491. This method is based on changing the scattering strength by changing the relative amount of light and heavy water in the microemulsion. 

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