Chromatographic performance of monolithic and particulate stationary phases. Hydrodynamics and adsorption capacity

Monolithic chromatographic support structures offer, as compared to the conventional particulate materials, a unique combination of high bed permeability, optimized solute transport to and from the active surface sites and a high loading capacity by the introduction of hierarchical order in the interconnected pore network and the possibility to independently manipulate the contributing sets of pores. While basic principles governing flow resistance, axial dispersion and adsorption capacity are remaining identical, and a similarity to particulate systems can be well recognized on that basis, a direct comparison of sphere geometry with monolithic structures is less obvious due, not least, to the complex shape of theskeleton domain. We present here a simple, widely applicable, phenomenological approach for treating single-phase incompressible flow through structures having a continuous, rigid solid phase. It relies on the determination of equivalent particle (sphere) dimensions which characterize the corresponding behaviour in a particulate, i.e. discontinuous bed. Equivalence is then obtained by dimensionless scaling of macroscopic fluid dynamical behaviour, hydraulic permeability and hydrodynamic dispersion in both types of materials, without needing a direct geometrical translation of their constituent units. Differences in adsorption capacity between particulate and monolithic stationary phases show that the silica-based monoliths with a bimodal pore size distribution provide, due to the high total porosity of the material of more than 90%, comparable maximum loading capacities with respect to random-close packings of completely porous spheres.     

Mikroreflexionsmessungen zur Untersuchung dünner Oberflächenschichten

Zusammenfassung Es wird eine einfache optische Methode zur Dickenbestimmung dünner Oberflächenfilme beschrieben, die sich besonders zur Untersuchung von Korrosionsschichten eignet.

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Investigation of thin corrosion layers by microreflexion measurement

A simple optical method for the determination of thin surface films is described. It is especially suitable for the thin corrosion layer investigation.

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Mit 1 Abbildung

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Meinem verehrten Lehrer, Prof. Dr.H. Nowotny, gewidmet.     

X-ray determination of the mean amplitudes of vibration and debye temperatures of some rare earth monochalcogenides

The x-ray diffraction intensities of Bragg reflections have been measured at room temperature for thulium selenide, samarium sulphide, samarium selenide and samarium telluride. On the basis of a common amplitude approximation, the Debye-Waller factor, the mean amplitude of vibration and the Debye temperature have been evaluated. The values of the Debye temperatures and mean amplitudes of vibration are 176±16°K, 0·185 ± 0·017 Å (TmSe), 155 ± 7°K, 0·244 ± 0·012 Å (SmS), 153 ± 14°K, 0·221 ± 0·020 Å (SmSe) and 151 ± 20°K, 0·204 ± 0·027 Å (SmTe).     

Physical nucleon properties from lattice QCD

We investigate various resummations of the chiral expansion and fit to the extremely accurate lattice QCD data for the mass of the nucleon recently obtained by the CP-PACS group. Using a variety of finite-range regulators, we demonstrate a remarkably robust chiral extrapolation of the nucleon mass. The systematic error associated with the chiral extrapolation alone is estimated to be less than 1%.     

Self-organized criticality and stock market dynamics: an empirical study

The stock market is a complex self-interacting system, characterized by intermittent behaviour. Periods of high activity alternate with periods of relative calm. In the present work we investigate empirically the possibility that the market is in a self-organized critical state (SOC). A wavelet transform method is used in order to separate high activity periods, related to the avalanches found in sandpile models, from quiescent. A statistical analysis of the filtered data shows a power law behaviour in the avalanche size, duration and laminar times. The memory process, implied by the power law distribution of the laminar times, is not consistent with classical conservative models for self-organized criticality. We argue that a “near-SOC” state or a time dependence in the driver, which may be chaotic, can explain this behaviour.     

Taking compact NMR to monitoring real reactions in large-scale chemical industries—General considerations and learnings from a lab-scale test case

The considerations for use of compact nuclear magnetic resonance in a large-scale industrial environment clearly differ from those in academic and educational settings and even from those in smaller companies. In the first part of this article, these differences will be discussed along with the additional requirements that need to be fulfilled for successful applicability in different use cases. In the second part of the article, outcomes from different research activities aiming to fulfill these requirements will be presented with a focus on an online reaction-monitoring study on a lab-scale nucleophilic chlorination reaction.