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Jörg Kärger

Publications and source records attributed to Jörg Kärger.

At least 19 recordsLinked to original sources
PubMed2006

Internal concentration gradients of guest molecules in nanoporous host materials: measurement and microscopic analysis.

Evolution of internal concentration profiles of methanol in 2-D pore structure of ferrierite crystal was measured in the pressure range of 0 to 80 mbar with the help of the recently developed interference microscopy technique. The measured profiles showed that both a surface barrier and internal diffusion controlled the kinetics of adsorption/desorption. Furthermore, they indicated that in the main part of the crystal, the z-directional 10-ring channels were not accessible to methanol and that the transport of methanol mainly occurred via 8-ring y-directional channels. The roof-like part of the crystal was almost instantaneously filled/emptied during adsorption/desorption, indicating accessible 10-ring channels in this section. The measured profiles were analyzed microscopically with the direct application of Fick's second law, and the transport diffusivity of methanol in ferrierite was determined as a function of adsorbed phase concentration. The transport diffusivity varied by more than 2 orders of magnitude over the investigated pressure range. Transport diffusivities, calculated from measured profiles from small and large pressure step changes, were all found to be consistent. Simulated concentration profiles obtained from the solution of Fick's second law with the calculated functional dependence of diffusivities on concentration compared very well with the measured concentration profiles, indicating validity and consistency of the measured data and the calculated diffusivities. The results indicate the importance of measuring the evolution of concentration profiles as this information is vital in determining (1) the direction of internal transport, (2) the presence of internal structural defects, and (3) surface/internal transport barriers. Such detailed information is available neither from common macroscopic methods since, they measure changes in macroscopic properties and use model assumptions to predict the concentration profiles inside, nor from microscopic methods, since they only provide information on average displacement of diffusing molecules.

Journal Article↗
PubMed2006

Exploration of molecular dynamics during transient sorption of fluids in mesoporous materials.

In recent years, considerable progress has been made in the development of novel porous materials with controlled architectures and pore sizes in the mesoporous range. An important feature of these materials is the phenomenon of adsorption hysteresis: for certain ranges of applied pressure, the amount of a molecular species adsorbed by the mesoporous host is higher on desorption than on adsorption, indicating a failure of the system to equilibrate. Although this phenomenon has been known for over a century, the underlying internal dynamics responsible for the hysteresis remain poorly understood. Here we present a combined experimental and theoretical study in which microscopic and macroscopic aspects of the relaxation dynamics associated with hysteresis are quantified by direct measurement and computer simulations of molecular models. Using nuclear magnetic resonance techniques and Vycor porous glass as a model mesoporous system, we have explored the relationship between molecular self-diffusion and global uptake dynamics. For states outside the hysteresis region, the relaxation process is found to be essentially diffusive in character; within the hysteresis region, the dynamics slow down dramatically and, at long times, are dominated by activated rearrangement of the adsorbate density within the host material.

Journal Article↗
PubMed2006

Two-component desorption from anisotropic pore networks.

Dynamic Monte Carlo simulations are performed to explore molecular desorption of a two-component mixture from a mode adsorbent of adsorbate-related anisotropy. The intrinsic dynamics of the adsorbent-adsorbate host-guest system is described by assuming a situation typical of a "molecular-traffic-control" system, where the hopping rates of the two components in two directions, perpendicular to each other, are identical, while for each component, perpendicular to that direction of preferential propagation, the hopping rates are reduced. The resulting desorption patterns are discussed in terms of the jump probabilities and are shown to approach the corresponding analytical solutions in the limiting cases of isotropic and unidirectional diffusions.

Journal Article↗
PubMed2005

Lambert diffusion in porous media in the Knudsen regime: equivalence of self-diffusion and transport diffusion.

We study molecular diffusion in nanopores with different types of roughness under the exclusion of mutual molecular collisions, i.e., in the so-called Knudsen regime. We show that the diffusion problem can be mapped onto Levy walks and discuss the roughness dependence of the diffusion coefficients D(s) and D(t) of self- and transport diffusion, respectively. While diffusion is normal in d=3, diffusion is anomalous in d=2 with D(s) approximately ln t and D(t) approximately ln L, where t and L are time and system size, respectively. Both diffusion coefficients decrease significantly when the roughness is enhanced, in remarkable disagreement with earlier findings.

Journal Article↗
PubMed2005

Sticking probability on zeolites.

The sticking coefficient, i.e., the probability that, on hitting the surface of a nanoporous particle (zeolite), a molecule shall be able to enter the intracrystalline space, is a key quantity for the application of such materials in heterogeneous catalysis and molecular sieving. On the basis of pulsed field gradient NMR diffusion measurements and molecular dynamics simulations, typical values of this probability are found to be close to one. They exceed previous estimates on the basis of IR uptake measurements by many orders of magnitude.

Journal Article↗
PubMed2005

Surface self-diffusion of organic molecules adsorbed in porous silicon.

The pulsed field gradient nuclear magnetic resonance method has been employed to probe self-diffusion of organic guest molecules adsorbed in porous silicon with a 3.6 nm pore size. The molecular self-diffusion coefficient and intrapore adsorption were simultaneously measured as a function of the external vapor pressure. The latter was varied in a broad range to provide pore loading from less than monolayer surface coverage to full pore saturation. The measured diffusivities are found to be well-correlated with the adsorption isotherms. At low molecular concentrations in the pores, corresponding to surface coverages of less than one monolayer, the self-diffusion coefficient strongly increases with increasing concentration. This observation is attributed to the occurrence of activated diffusion on a heterogeneous surface. Additional experiments in a broad temperature range and using binary mixtures confirm this hypothesis.

Journal Article↗
PubMed2005

Concentration-dependent self-diffusion of adsorbates in mesoporous materials.

The pulsed-field gradient NMR method has been applied to study self-diffusion of liquids in mesoporous materials with different pore sizes and morphologies as a function of pore loading. It is found that the effective diffusivities of adsorbate molecules in mesopores at partial loadings are related to two mechanisms, the Knudsen diffusion through the gaseous phase in the pore space and the diffusion within the layer of molecules adsorbed on the pore walls. The relative contributions of these modes, which are determined by the details of the interphase equilibrium, change with variation of the pore loading, leading to a complex behavior of the effective self-diffusion coefficient. The impact of the pore size and the adsorbate-surface interaction on self-diffusion is elucidated. Possible reasons for an experimentally obtained hysteresis in the diffusivities measured on adsorption and desorption in mesopores are discussed.

Adsorption↗
PubMed2005

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↗
PubMed2005

Long-range diffusion in beds of nanoporous particles: pitfalls and potentials.

Owing to the recent progress in the area of hardware and software of the pulsed field gradient NMR technique, molecular transport in real-life zeolite systems, such as zeolite beds and particles of formulated fluid catalytic cracking (FCC) catalysts, can be investigated in detail. These studies have revealed a number of important features of molecular transport in zeolites, which are reviewed in the present paper. In particular, the anomalous character of intracrystalline diffusion in MFI-type zeolites, dependence of the tortuosity factor in zeolite beds on diffusion regime and the role of various modes of diffusion in transport limitations arising for catalytic reactions in FCC catalysts will be discussed.

Diffusion↗
PubMed2004

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↗
PubMed2004

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↗
PubMed2004

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↗
PubMed2002

Different time regimes of tracer exchange in single-file systems.

A complete description of the time dependence of tracer exchange in single-file systems is given. It is based on the combined application of dynamic Monte Carlo simulations and analytical calculations. Depending on the time elapsed, the tracer exchange is found to have different time scaling related to transport modes of either normal diffusion or single-file diffusion. The mode of single-file diffusion is reproduced by recent tracer exchange experiments conducted by laser-polarized 129Xe NMR spectroscopy.

Journal Article↗
PubMed2002

Regular intergrowth in the AFI-type crystals: influence on the intracrystalline adsorbate distribution as observed by interference and FTIR-microscopy.

Interference microscopy and FTIR microscopy are applied to study intracrystalline concentration profiles of methanol in CrAPO-5 zeolite crystals. By using both techniques, the high spatial resolution of interference microscopy is complemented by the ability of FTIR spectroscopy to pinpoint adsorbates by their characteristic IR bands. For the first time two-dimensional concentration profiles of an unprecedented quality are reported which show a nonhomogeneous distribution of adsorbate in zeolite crystal under equilibrium with the adsorbate vapor. These nonhomogeneous profiles are attributed to regular intergrowth effects in CrAPO-5. A possible internal structure of CrAPO-5 crystals is suggested.

Journal Article↗
PubMed2002

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↗
PubMed2002

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↗