Effects of type of radiation on glow curve and thermoluminescence emission spectrum of CaF2:Tm

Thermoluminescence emission spectra of CaF₂:Tm (TLD-300) samples irradiated with 48 keV X-rays ⁶⁰Co gamma rays, 4.5 MeV alpha particles and 15 MeV neutrons were measured in the 300–650 K temperature region. Seven emission bands were observed of which the one in the infrared (at 803 nm) is very intense. The emission bands can be assigned to ¹D, ¹G, ³F and ³H levels characteristic for Tm³⁺ de-excitation in a cubic field. All observed lines in the spectrum are due to 4f-4f transitions. The spectra undergo remarkable changes in intensity when the temperature is raised from room temperature up to 350°C, while the number of the emission bands remains constant. The glow curve structure is both dependent on emission wavelength and the type of radiation. Evidence has been found that the trapping structures responsible for glow peaks 2 and 3 alter under the influence of high LET () radiation. For glow peaks 4–6 the filling of the traps alters with the type of radiation. The observations can be explained assuming a TL process involving several hole trapping centres but with only one luminescent centre (Tm³⁺) active at all temperatures.     

Determination of sulphhydryl compounds in physiological fluids by liquid chromatography with polarographic detection

Summary A polarographic detector with a horizontal, fast dropping mercury electrode has been applied for the determination of thiols in physiological fluids. To establish suitable detection conditions first some basic studies on the polarographic behaviour of penicillamine, glutathione and cysteine were performed. This type of detection shows a high selectivity and reasonably low detection limits for sulphhydryl compounds. Detection limits of 6×10^–7 mol l^–1 for penicillamine and cysteine and 8×10^–7 mol l^–1 for glutathione were found. A good linearity has been observed over a concentration range of three orders. The detector has successfully been applied to the determination of penicillamine in urine and serum samples.

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Bestimmung von Sulfhydrylverbindungen in physiologischen Flüssigkeiten durch Flüssigkeits-Chromatographie mit polarographischer Detektion

Zusammenfassung Ein polarographischer Detektor mit horizontaler, schnell tropfender Quecksilberelektrode wurde zur Bestimmung von Thiolen in physiologischen Flüssigkeiten angewendet. Zur Feststellung geeigneter Bedingungen wurden zunächst grundlegende Untersuchungen zum polarographischen Verhalten von Penicillamin, Glutathion und Cystein durchgeführt. Das Verfahren bietet hohe Selektivität und niedrige Nachweisgrenzen (6 · 10^–7 mol/l für Penicillamin und Cystein, 8 · 10^–7 mol/l für Glutathion). Linearität besteht über drei Größenordnungen. Der Detektor wurde mit gutem Erfolg für die Penicillaminbestimmung in Harn und Serum verwendet.

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Dedicated to Prof. Dr. H. Weisz on occasion of his 60th birthday

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On leave from the Technical University of Gdansk     

Die Einbettung von Mittelwertstrukturen in Q-Vektorräume

Ohne Zusammenfassung     

Some applications of enthalpimetric detection in flow injection analysis

Summary A flow injection manifold is described based on a flow-through arrangement of thermistors for measuring heat effects of chemical reactions. Temperature changes down to 10^–3 °C can be measured reproducibly. The working range for the determination of a component is dependent on the reaction enthalpy and can vary from 10^–3 to 10 mol/l for acids and bases, from 10 to 1000 ppm for e.g., alkylhydroperoxides. Sample frequencies up to 150 samples per hour can be realized.

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Einige Anwendungen der enthalpimetrischen Detektion in der Fließinjektionsanalyse

     

Kergin interpolants at the roots of unity approximate C2 functions

We establish a new formula for Kergin interpolation in the plane and use it to prove that the Kergin interpolation polynomials at the roots of unity of a function of classC ² in a neighborhood of the unit disc converge uniformly to the function on .     

Facile Surfactant‐Free Synthesis of p‐Type SnSe Nanoplates with Exceptional Thermoelectric Power Factors

A surfactant‐free solution methodology, simply using water as a solvent, has been developed for the straightforward synthesis of single‐phase orthorhombic SnSe nanoplates in gram quantities. Individual nanoplates are composed of {100} surfaces with {011} edge facets. Hot‐pressed nanostructured compacts (E_g≈0.85 eV) exhibit excellent electrical conductivity and thermoelectric power factors (S²σ) at 550 K. S²σ values are 8‐fold higher than equivalent materials prepared using citric acid as a structure‐directing agent, and electrical properties are comparable to the best‐performing, extrinsically doped p‐type polycrystalline tin selenides. The method offers an energy‐efficient, rapid route to p‐type SnSe nanostructures.     

Acid-base strengths in 1,2-dichloroethane

The pK_a value of hydriodic acid in 1,2-dichloroethane was determined from conductivity measurements. A glass electrode was calibrated for dichloroethane in the potentiometric titration of hydriodic acid with tetramethylguanidine. From potentiometric titrations, the pK_a values in dichloroethane of hydrobromic acid, hydrochloric acid, picric acid and some sulfonphthaleins as well as some protonated nitrogen bases were determined. In the curves of the titrations of the carboxylic acids and the hydrogen halides with TMG, evidence was found for the formation of the complex B(HX)₂.     

Impulse/response functions of individual components of flow-injection manifolds

The dispersion behaviour of the various individual parts making up a flow-injection manifold is often difficult to establish because it is virtually impossible to obtainthe required very small injection and detection volumes. It is shown that it is possible, under suitable experimental conditions, to find the impulse/response functionof each component by means of a deconvolution process of the response functions have been established, the response function of any arrangement can be predicted by convoluting the impulse/response functions of all the individuaol parts involved. Convolution and deconvolution were done in the Fourier domain, by using a fast FT algorithm.