This paper discusses a new nuclear magnetic resonance (NMR) method that can provide wettability, saturation, and oil viscosity values in rocks partially saturated with oil and brine. The method takes advantage of two new technological advances in NMR well logging-the MRF* Magnetic Resonance Fluid Characterization Method and NMR "diffusion-editing" (DE) pulse sequences. We discuss the principles underlying the fluid characterization method and the pulse sequences. The fluid characterization method is used to provide robust inversions of DE data suites acquired on fully brine-saturated and partially saturated rock samples. The outputs of the inversion are separate diffusion-free brine and oil T 2 distributions for the fluids measured in the rocks.NMR measurements on partially saturated rocks are sensitive to wettability because of surface relaxation of the wetting-phase fluid. The surface relaxation rate, however, must be significant compared to the bulk relaxation rate in order for wettability to noticeably affect the NMR response. We present results showing that the surface relaxation rate at lower wetting-phase saturations is enhanced compared to that measured at higher saturations. The consequence of wetting-phase saturation on NMR-based wettability determination is discussed. Wettability affects the relaxation rates of both the wetting and nonwetting phases in partially saturated rocks. Surface relaxation of the wetting phase in a rock results in shorter relaxation times than would otherwise be observed for the bulk fluid. The nonwetting-phase fluid molecules do not come into contact with the pore surfaces, and therefore their relaxation rate in the rock is the same as in the bulk fluid.We present accurate and robust computations of diffusion-free T 2 relaxation time distributions for both the wetting and nonwetting phases in four rocks that include two sandstones and two dolomites. A DE data suite was acquired on each rock, measured in two different partial saturation states and also fully brinesaturated. Wettability is determined by comparing the oil and brine T 2 relaxation-time distributions measured in the partially saturated rocks with the bulk oil T 2 distribution and with the T 2 distribution of the fully brine-saturated sample. The brine and oil T 2 distributions are used to compute saturation and oil viscosity values.A general discussion elucidating the sensitivity range and T 2 limits of diffusion-based NMR methods is given in the appendix. The appendix also derives and displays the gain in signal-to-noise ratio that is achieved by using DE data sequences for fluid characterization in place of Carr-Purcell-Meiboom-Gill (CPMG) data suites.
The synthesis of several polyesters from p,p′-bibenzoic acid and diols bearing ether bonds in asymmetric positions is described. The polyesters develop smectic mesophases, the type of which depends on the chemical structure of the spacer. The ether groups and the asymmetry of the spacers stabilize the liquid crystalline order in these polymers. Glass transition and isotropization temperatures, enthalpies, and entropies of the thermotropic polyesters are reported. Comparison of the melting entropies with the conformational entropies of the chains suggests a great disorder in the mesophases of thermotropic polyesters. For some polyesters, the stretched polymer chains do not follow the direction of the fiber axis, an unusual phenomenon that has already been described for some polybibenzoates with aliphatic separators. The influence of the strain rate on the anomalous flow is discussed.
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