The Inclusion Properties of a New Watersoluble Sulfonated Calix[4]resorcinarene towards Alkylammonium and N-Methylpyridinium Cations

The inclusion behaviour of a new water-soluble sulfonated calix[4]resorcinarene towards alkylammonium and N-methylpyridinium cations has been investigated on the basis of ¹H NMR spectroscopy and pH-potentiometry data. The inclusion of the N-methylpyridinium cation has been found to be dependent on pH with the preferable inclusion of the methyl substituent in alkaline and the aromatic ring in neutral aqueous media.     

Korrosion und Schutzanstriche

Ohne Zusammenfassung     

Korrosionsuntersuchung

Ohne Zusammenfassung     

Rheology of a dilute suspension of axisymmetric Brownian particles

Explicit results are presented for the complete rheological properties of dilute suspensions of rigid, axisymmetric Brownian particles possessing fore-aft symmetry, when suspended in a Newtonian liquid subjected to a general three-dimensional shearing flow, either steady or unsteady. It is demonstrated that these rheological properties can be expressed in terms of five fundamental material constants (exclusive of the solvent viscosity), which depend only upon the sizes and shapes of the suspended particles. Expressions are presented for these scalar constants for a number of solids of revolution, including spheroids, dumbbells of arbitrary aspect ratio and long slender bodies. These are employed to calculate rheological properties for a variety of different shear flows, including uniaxial and biaxial extensional flows, simple shear flows, and general two-dimensional shear flows. It is demonstrated that the rheological properties appropriate to a general two-dimensional shear flow can be deduced immediately from those for a simple shear flow. This observation greatly extends the utility of much of the prior Couette flow literature, especially the extensive numerical calculations of Scheraga et al. (1951, 1955).The commonality of many disparate results dispersed and diffused in earlier publications is emphasized, and presented from a unified hydrodynamic viewpoint.     

Determination of trace elements in zeolites by laser ablation ICP-MS

Laser ablation inductively coupled plasma mass spectrometry using a quadrupole-based mass spectrometer (LA-ICP-QMS) was applied for the analysis of powdered zeolites (microporous aluminosilicates) used for clean-up procedures. For the quantitative determination of trace element concentrations three geological reference materials, granite NIM-G, lujavrite NIM-L and syenite NIM-S, from the National Institute for Metallurgy (South Africa) with a matrix composition corresponding to the zeolites were employed. Both the zeolites and reference materials were fused with a lithium borate mixture to increase the homogeneity and to eliminate mineralogical effects. In order to compare two different approaches for the quantification of analytical results in LA-ICP-MS relative sensitivity coefficients (RSCs) of chemical elements and calibration curves were measured using the geostandards. The experimentally obtained RSCs are in the range of 0.2-6 for all elements of interest. Calibration curves for trace elements were measured without and with Li or Ti as internal standard element. With a few exceptions the regression coefficients of the calibration curves are better than 0.993 with internal standardization. NIM-G granite reference material was employed to evaluate the accuracy of the technique. Therefore, the measured concentrations were corrected with RSCs which were determined using lujavrite reference material NIM-L. This quantification method provided analytical results with deviations of 1-11% from the recommended and proposed values in granite reference material NIM-G, except for Co, Cs, La and Tb. The relative standard deviation (RSD) of the determination of the trace element concentration (n = 5) is about 1% to 6% using Ti as internal standard element. Detection limits of LA-ICP-QMS in the lower microg/g range (from 0.03 microg/g for Lu, Ta and Th to 7.3 microg/g for Cu, with the exception of La) have been achieved for all elements of interest. Under the laser ablation conditions employed (lambda: 266 nm, repetition frequency: 10 Hz, pulse energy: 10 mJ, laser power density: 6 x 10(9) W/cm2) fractionation effects of the determined elements relative to the internal standard element Ti were not observed.     

The rationality of the Hilbert-Kunz multiplicity in graded dimension two

We show that the Hilbert-Kunz multiplicity is a rational number for an R₊−primary homogeneous ideal I=(f₁, . . . , f_n) in a two-dimensional graded domain R of finite type over an algebraically closed field of positive characteristic. More specific, we give a formula for the Hilbert-Kunz multiplicity in terms of certain rational numbers coming from the strong Harder-Narasimhan filtration of the syzygy bundle Syz(f₁, . . . , f_n) on the projective curve Y=ProjR.     

Evaluation of an ultrasonic nebulizer-membrane separation interface (USN-MEMSEP) with ICP-AES for the determination of trace elements by solvent extraction

The introduction of volatile organic solvents and metal organic complexes into an inductively coupled plasma (ICP) is problematic due to overloading and pyrolysis effects. These include carbon built up in the torch and spectral interferences. As a consequence, solvent extraction as a method for preconcentrating trace metals for the determination by ICP has been limited. In this report a commercial ultrasonic nebulizer-membrane separation interface (USN-MEMSEP) for the direct introduction and separation of organic solvents using ICP atomic emission spectrometry (AES) and a sequential spectrometer has been evaluated for solvent extraction of chelated trace metals. The ability of the MEMSEP to separate volatile organic flows from metal aerosols has been demonstrated by determining the recoveries of several transition metals in an oil-based methyl-isobutyl ketone (MIBK) standard relative to an aqueous solution. However, low recoveries of several metal chelates have been found evidently due to the volatilization of the organic metal species at the boiling point of MIBK (160° C). Moreover, the multielement capability and limits of detection have been limited due to sequential atomic emission detection. Advantages of the technique include enhanced limits of detection (LODs) and reduced plasma and spectral interferences.