Measuring Diffusion with NMR

The ambient-pressure diaphragm-cell method was adapted and developed for high-pressure measurements by Woolf and co-workers in the 1970s. It retains the simplicity of the ambient-pressure glass diaphragm cell and has been used to obtain self-diffusion and intradiffusion coefficients over a wide temperature and pressure range to an accuracy of 1-2 per cent, which is in excellent agreement with self-diffusion measurements made with NMR techniques. 

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 ... 

We finish this section by comparing our results with NMR and incoherent neutron scattering experiments on water dynamics. Self-diffusion constants on the millisecond time scale have been measured by NMR with the pulsed field gradient spin echo (PFGSE) method. Applying this technique to oriented egg phosphatidylcholine bilayers, Wassail [68] demonstrated that the water motion was highly anisotropic, with diffusion in the plane of the bilayers hundreds of times greater than out of the plane. The anisotropy of... 

Johnson et al. [186] measured diffusion of fluorescein-labeled macromolecules in agarose gels. Their data agreed well with Eq. (85), which combined the hydrodynamic effects with the steric hindrance factors. Gibbs and Johnson [131] measured diffusion of proteins and smaller molecules in polyacrylamide gels using pulsed-field gradient NMR methods and found their data to fit the stretched exponential form... 

Fig. 3.1.5 Temperature dependence of the coefficient of long-range self-diffusion of ethane measured by PFG NMR in a bed of crystallites of zeolite NaX (points) and comparison with the theoretical estimate (line). The theoretical estimate is based on the sketched models of the prevailing Knudsen diffusion...

Comparison between xf a as determined on the basis of Eq. (3.1.15) from the microscopically determined crystallite radius and the intracrystalline diffusivity measured by PFG NMR for sufficiently short observation times t (top left of Figure 3.1.1), with the actual exchange time xintra resulting from the NMR tracer desorption technique, provides a simple means for quantifying possible surface barriers. In the case of coinciding values, any substantial influence of the surface barriers can be excluded. Any enhancement of xintra in comparison with x a, on the other side, may be considered as a quantitative measure of the surface barriers. 

Accurate interpretation of the formation properties (porosity, permeability and irreducible water saturation) requires reliable estimates of NMR fluid properties or the relationship between diffusivity and relaxation time. Estimation of oil viscosity and solution-gas content require their correlation with NMR measurable fluid properties. These include the hydrogen index, bulk fluid relaxation time and bulk fluid diffusivity [8]. 

NMR interpretation has made significant advances with diffusion-editing pulse sequences and two-dimensional inversion of diffusivity and T2 relaxation [7,40-44]. The 2D inversion can also be used to compare Tj and T2 relaxation with each other [42]. Distributions of these two characteristic parameters can now be displayed on a 2D map and the relationship between them more easily visually interpreted. The 2D distribution map can be interpreted by comparing the measured distribution with the line for the bulk diffusivity of water and the correlation lines for the hydrocarbon components in crude oils, shown in Figure 3.6.10 as dashed lines [40-46]. Figure... 

Three types of methods are used to study solvation in molecular solvents. These are primarily the methods commonly used in studying the structures of molecules. However, optical spectroscopy (IR and Raman) yields results that are difficult to interpret from the point of view of solvation and are thus not often used to measure solvation numbers. NMR is more successful, as the chemical shifts are chiefly affected by solvation. Measurement of solvation-dependent kinetic quantities is often used (<electrolytic mobility, diffusion coefficients, etc). These methods supply data on the region in the immediate vicinity of the ion, i.e. the primary solvation sphere, closely connected to the ion and moving together with it. By means of the third type of methods some static quantities entropy and compressibility as well as some non-thermodynamic quantities such as the dielectric constant) are measured. These methods also pertain to the secondary solvation-sphere, in which the solvent structure is affected by the presence of ions, but the... 

The reduction of the long-range diffusivity, Di by a factor of four with respect to bulk water can be attributed to the random morphology of the nanoporous network (i.e., effects of connectivity and tortuosity of nanopores). For comparison, the water self-diffusion coefficient in Nafion measured by PFG-NMR is = 0.58 x 10 cm s at T = 15. Notice that PFG-NMR probes mobilities over length scales > 0.1 /rm. Comparison of QENS and PFG-NMR studies thus reveals that the local mobility of water in Nafion is almost bulk-like within the confined domains at the nanometer scale and that the effective water diffusivity decreases due to the channeling of water molecules through the network of randomly interconnected and tortuous water-filled domains. ... 

An account has now appeared in which the domain-domain alignment determined using RDCs exhibits potential discrepancies with the alignment determined using NMR rotational diffusion measurements. In a study on polyubiquitin chains, Fushman and co-workers found small differences in the relative alignment of two ubiquitin units in Ub2 determined using RDCs and rotational diffusion measurements.124 The NMR study... 

Tanner [49] measured diffusion coefficients of water in three different types of frog muscle cells. He used a variety of magnetic field gradient techniques so as to cover a wide range of diffusion times A= 1 ms to 1 s. The time dependence of the diffusion coefficient was analyzed to obtain the intracellular diffusion coefficients and estimates of the permeability of the cell membranes. In restricted diffusion studies three 90 degree r.f. pulse sequences (stimulated echo) are often used which provides PG-NMR experiments with long diffusion times to explore the dependence of diffusion time on the echo attenuation [49]. 

Counterion binding is not a well defined quantity, with various experimental techniques weighing the ion distribution slightly differently. Thermodynamic methods (e.g. ion activities or osmotic coefficients) monitor the free counterion concentration, transport methods (e.g. ion self diffusion or conductivity) the counterions diffusing with the micelle, and spectroscopic methods (e.g. NMR) the counterions in close contact with the micelle surface. Measurement of the effect of Na+ counterions on the symmetric S-O stretching modes would also be expected to be highly dependent on the distance of the counterion from the micelle surface (similar to the NMR method). 

Almost all of these examples involve diffusion of a chemical species measuring diffusion rates has long been a specialty of NMR spectroscopy. The studies of KBr and drawn polyethylene produced unique information in the latter case, the known orientation of the deuterium electric field gradient in C-D bonds is used to determine the orientation, with respect to the magnetic field, of a polymer chain of a uniaxially ordered polyethylene fiber. The real time imaging of the polymerization of methyl methacrylate is very interesting and may represent a major direction for NMR imaging applications to polymer science. 

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Diffusion of hydrocarbons and other simple molecules in A, X and Y zeolites has been studied by a range of experimental methods including direct sorption rate measurements, chromatography and NMR. The advantages and limitations of these techniques are considered and results of recent experimental studies are reviewed with emphasis on the detailed microdynamic information obtainable by NMR. 

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