NMR studies on the diffusion of hydrocarbons on the metal-organic framework material MOF-5.
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Journal Article↗
Biomedical subjects
Frank Stallmach
Publications and source records attributed to Frank Stallmach.
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. The column of the adsorbent material is placed in the sensitive region of the superconducting magnet and the rf coil of the NMR spectrometer. The time scales of the adsorption and desorption processes depend on concentration, temperature and crystal shape and are found to be in the range of 1-10 min. From the desorption branch, the non-equilibrium ZLC-NMR measurements yield intracrystalline diffusion coefficients in the range of 10(-13) to 10(-11) m2/s for different alkanes in silicalite-1. These values are always found to be smaller than the values measured by pulsed field gradient NMR under equilibrium condition indicating that there must be additional transport resistance at the external surface of these silicalite-1 zeolite crystals.
Adsorption↗
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. Our experimental results demonstrate that the microscopic mechanisms of proton conductivity in this system are effective on a time scale ranging from nanosecond to picosecond. In the present paper, we discuss more specifically on the relaxation processes occurring on a nanosecond time scale by combining high-resolution quasielastic neutron scattering and 1H pulse-field-gradient nuclear magnetic resonance experiments. The combination of these two techniques allows us to probe proton dynamics in both space and time domains. The existence of two types of proton dynamical processes has been identified. The slowest one is associated to long-range translational diffusion of protons between crystallographic oxygen sites and has been precisely characterized with a self-diffusion coefficient of 3.5 x 10(-8) cm2/s at 220 K and an activation energy of 29.2+/-1.4 kJ/mol. The fastest dynamical process is due to water molecules' reorientations occurring every 0.7 ns at 220 K with an activation energy of 17.4+/-1.5 kJ/mol. This powerful multitechnique approach provides important information required to understand the microscopic origin of proton transport in an ionic clathrate hydrate.
Journal Article↗
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. The methods used in the studies were NMR relaxometry and pulsed field gradient (PFG) NMR diffusometry. To study selectively the behavior of the non-aqueous-phase liquid (NAPL) phases, heavy water was used in the preparation of the cement pastes. The experimental results are in good agreement with the observations from earlier studies concerning the behavior of toluene in hydrating cement. For aliphatic solvents (cyclooctane, n-hexanol), indications for surprisingly large networks of connected droplets in the cement matrices are found.
Construction Materials↗
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. These techniques are based on (i) the measurement of the effective diffusivity under complete confinement, (ii) the application of the so-called NMR tracer desorption technique, and (iii) an analysis of the time dependence of the effective diffusivity in the short-time limit where, by an appropriate variation of the adsorbate and the measuring conditions, the limiting cases of reflecting and adsorbing boundaries could be considered. All these techniques are found to yield coinciding results, which are in excellent agreement with the crystal sizes determined by microscopy.
Journal Article↗
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)]. Since the width of the pulsed field gradients (delta) is bounded by 0< or =delta< or =tau, eta can only be in the range of 5< or =-eta< or =7. The predicted suppression of the unwanted cross terms is demonstrated experimentally using time-dependent external gradients which are controlled in the NMR experiment as well as spatially dependent internal background gradients generated by the magnetic properties of the sample itself. The theoretical and experimental results confirm and extend the approach of Sun et al. (J. Magn. Reson. 161 (2003) 168), who recently introduced a 13-interval type PFG NMR sequence with two asymmetric pulsed magnetic field gradients suitable to suppress unwanted cross terms with spatially dependent background field gradients.
Diffusion↗
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. The observed self-diffusion coefficients decrease with increasing molecular weights of the polymers and with a decreasing water content of the cartilage. In contrast, the long-time self-diffusion coefficients of the polymers in cartilage (diffusion time Delta approximately 600 ms) reflect the structural properties of the tissue. Measurements at different water contents, different molecular weights of the polymers and varying observation times suggest that primarily the collagenous network of cartilage but also the entanglements of the polymer chains themselves are responsible for the observed restricted diffusion. Additionally, anomalous restricted diffusion was shown to occur already in concentrated polymer solutions.
Animals↗
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) = -0.70+/-0.05 and D(s) = 2.20+/-0.05. The results demonstrate that NMR studies with native pore fluids are suitable to investigate the fractal nature of natural, unconsolidated porous materials.
Journal Article↗
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.
Adsorption↗