Restricted self-diffusion of adsorbed water in MIL-100(Al).

An extended two-site exchange model is presented, which is used to evaluate pulsed field gradient (PFG) nuclear magnetic resonance (NMR) measurements of water in the nanoporous metal-organic framework MIL-100(Al). Here the water molecules exchange between the inter- and the intracrystalline space during the observation time, but are also restricted in their movement by the crystal surface. The evaluation of temperature and loading dependent PFG NMR data yields information about the intracrystalline diffusion process, the radius of the restricting geometry and the time constants of the exchange process.

Development and application of an exchange model for anisotropic water diffusion in the microporous MOF aluminum fumarate.

Diffusion of water in aluminum fumarate was studied by means of pulsed field gradient (PFG) nuclear magnetic resonance (NMR). Due to water molecules exchanging between the intracrystalline anisotropic pore space and the isotropic intercrystalline void space the model of intracrystalline anisotropic diffusion fails to describe the experimental PFG NMR data at high observation times. Therefore, the two-site exchange model developed by Kärger is extended to the case of exchange between an anisotropic and an isotropic site.

Temperature dependence of water diffusion pools in brain white matter.

Water diffusion in brain tissue can now be easily investigated using magnetic resonance (MR) techniques, providing unique insights into cellular level microstructure such as axonal orientation. The diffusive motion in white matter is known to be non-Gaussian, with increasing evidence for more than one water-containing tissue compartment. In this study, freshly excised porcine brain white matter was measured using a 125-MHz MR spectrometer (3T) equipped with gradient coils providing magnetic field gradients of up to 35,000 mT/m.

High-pressure low-field 1H NMR relaxometry in nanoporous materials.

A low-field NMR sensor with NdFeB permanent magnets (B0=118 mT) and a pressure cell made of PEEK (4 cm outer diameter) were designed for (1)H relaxation time studies of adsorbed molecules at pressures of up to 300 bar. The system was used to investigate methane uptake of microporous metal-organic frameworks and nanoporous activated carbon. T2 relaxation time distribution of pure methane and of methane under co-adsorption of carbon dioxide show that the host-guest interaction lead to a relaxation time contrasts, which may be used to distinguish between the gas phase and the different adsorbed phases of methane.

X-Nuclei NMR Self-Diffusion Studies in Mesoporous Silica Foam and Microporous MOF CuBTC.

A standard X-observe NMR probe was equipped with a z-gradient coil to enable high-sensitivity pulsed field gradient NMR diffusion studies of Li⁺ and Cs⁺ cations of aqueous salt solutions in a high-porosity mesocellular silica foam (MCF) and of CO₂ adsorbed in metal-organic frameworks (MOF). The coil design and the necessary probe modifications, which yield pulsed field gradients of up to ±16.2Tm, are introduced.

Self-Diffusion of Chain Molecules in the Metal-Organic Framework IRMOF-1: Simulation and Experiment.

Metal-organic frameworks (MOFs) possess characteristics, such as tunable pore size and chemical functionality, that make them attractive candidates for separations, catalysis, gas storage, and sensing applications. The rate of diffusion of guest molecules in the pores is an important property for all of these potential applications. In this work, the self-diffusion of hydrocarbons in IRMOF-1 was studied as a function of chain length with a combination of molecular dynamics simulations and pulsed field gradient NMR experiments.

Paramagnetic relaxation enhancement (PRE) as a tool for probing diffusion in environmentally relevant porous media.

The transport diffusivity of the paramagnetic molecule 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) was measured by monitoring its influence on the NMR transverse relaxation time (T₂) on surrounding water protons - also known as paramagnetic relaxation enhancement (PRE). Due to the nature of the PRE effect, few paramagnetic molecules are able to simultaneously reduce the T₂ of many NMR active nuclei, which represents a significant gain in sensitivity. In an aqueous solution, the minimal detectable TEMPO concentration was around 70 ppm.

The self-diffusion behavior of polyethylene glycol in cartilageas studied by pulsed-field gradient NMR.

The self-diffusion behavior of the polyethylene glycol (PFG) polymer in bovine nasal cartilage was studied by pulsed-field gradient (PFG) nuclear magnetic resonance (NMR). PFG NMR allows the determination of the mean square displacement of molecules in a given diffusion time (in the range of a few milliseconds up to seconds), monitors distances in micrometer scales and has the advantage of being non-invasive. Moreover the application of pfg nmr does not require concentration gradients In a previous study, PFG NMR was used to investigate the self-diffusion behavior of the PEG polymer in cartilage at very highconcentrations.

Combining macroscopic and microscopic diffusion studies in zeolites using NMR techniques.

In this study the zero length column (ZLC) technique is extended to the case where the decay of the adsorbed phase concentration is observed directly by nuclear magnetic resonance (NMR). An adsorption-desorption apparatus compatible with a 400-MHz NMR spectrometer was developed. It operates with nitrogen or helium as the inert purge gas.

Proton dynamics in the perchloric acid clathrate hydrate HClO4.5.5H2O.

In the perchloric acid clathrate hydrate HClO4.5.5H2O, the perchlorate anions are contained inside an aqueous host crystalline matrix, positively charged because of the presence of delocalized acidic protons.

Boundary effects of molecular diffusion in nanoporous materials: a pulsed field gradient nuclear magnetic resonance study.

The boundary conditions of intraparticle diffusion in nanoporous materials may be chosen to approach the limiting cases of either absorbing or reflecting boundaries, depending on the host-guest system under study and the temperature of measurement. Pulsed field gradient nuclear magnetic resonance is applied to monitor molecular diffusion of n-hexane and of an n-hexane-tetrafluoromethane mixture adsorbed in zeolite crystallites of type NaX under either of these limiting conditions. Taking advantage of the thus-established peculiarities of mass transfer at the interface between the zeolite bulk phase and the surrounding atmosphere, three independent routes for probing the crystal size are compared.

Direct investigation of the fate of NAPL contaminations in a hydrating cement matrix by means of magnetic resonance techniques.

The behavior of nonwatery solvent phases in hydrating cement pastes is of great interest in the context of solidification of wastes containing such phases. In a recent study, the influence of various solvents on the hydration kinetics of cement was studied. In this paper, we present results on the changes in the behavior of the solvent phases themselves during setting of the cement pastes.

Background gradient suppression in stimulated echo NMR diffusion studies using magic pulsed field gradient ratios.

By evaluating the spin echo attenuation for a generalized 13-interval PFG NMR sequence consisting of pulsed field gradients with four different effective intensities (F(p/r) and G(p/r)), magic pulsed field gradient (MPFG) ratios for the prepare (G(p)/F(p)) and the read (G(r)/F(r)) interval are derived, which suppress the cross term between background field gradients and the pulsed field gradients even in the cases where the background field gradients may change during the z-store interval of the pulse sequence. These MPFG ratios depend only on the timing of the pulsed gradients in the pulse sequence and allow a convenient experimental approach to background gradient suppression in NMR diffusion studies with heterogeneous systems, where the local properties of the (internal) background gradients are often unknown. If the pulsed field gradients are centered in the tau-intervals between the pi and pi/2 rf pulses, these two MPFG ratios coincide to eta=G(p/r)/F(p/r)=1-8/[1+(1/3)(delta/tau)(2)].

Structure-mobility relations of molecular diffusion in nanoporous materials.

Depending on the measuring conditions, pulsed field gradient (PFG) NMR measurements of molecular diffusion in beds of nanoporous particles may provide information about the propagation rate of guest molecules in both the intra- and interparticle spaces, as well as through the interface between them. Recent progress in both PFG NMR instrumentation and computational techniques have initiated studies of novel aspects in each of these areas, which are reviewed in this communication. They concern the possibility of multicomponent diffusion measurements with ultra-high pulsed field gradients, the peculiarities of molecular diffusion in channel networks, the determination of the surface-to-volume ratio of nanoporous particles and the dependence of the tortuosity factor of long-range diffusion on the diffusion mode in the intercrystalline space.

Self-diffusion of polymers in cartilage as studied by pulsed field gradient NMR.

Pulsed field gradient (PFG) nuclear magnetic resonance (NMR) was used to investigate the self-diffusion behaviour of polymers in cartilage. Polyethylene glycol and dextran with different molecular weights and in different concentrations were used as model compounds to mimic the diffusion behaviour of metabolites of cartilage. The polymer self-diffusion depends extremely on the observation time: The short-time self-diffusion coefficients (diffusion time Delta approximately 15 ms) are subjected to a rather non-specific obstruction effect that depends mainly on the molecular weights of the applied polymers as well as on the water content of the cartilage.

Fractal geometry of surface areas of sand grains probed by pulsed field gradient NMR.

Pulsed field gradient NMR self-diffusion studies of water were used to determine surface-to-volume ratios and specific surface areas of the grains forming a glacial sand deposit. Both quantities exhibit a noninteger power-law dependence as a function of the diameters of the grains. The associated fractal dimensions of the surface area ( D(s)) and of the pore volume ( D(v)) are found to be D(s)-D(v) = -0.