Depolymerization of polysulfide polymers by dithionite ions

The action of sodium dithionite, Na₂S₂O₄ on desulfurized tetrasulfide polymers leads to their depolymerization. Our studies showed that successful depolymerization can be initiated only in an alkali medium when 1.9–3.2 mole of sodium hydroxide per mole of dithionite is used, and that this leads to the cleavage of disulfide bonds and the formation of polymers of lower molecular weight with ? SH end groups. Liquid polymers of 1000–5000 molecular weight are obtained when 0.388–0.155 mole sodium dithionite per segment of polymer is used for depolymerization in the presence of the above-mentioned quantity of sodium hydroxide per mole of dithionite. The depolymerization of poly-sulfide polymers with sodium dithionite in the presence of sodium hydroxide was followed by determination of the molecular weight and sulfur content of the polymer and analysis of the mother liquid.     

Microquantitative determination of hesperidin by pulse perturbation of the oscillatory reaction system

A simple and reliable kinetic method for the determination of hesperidin (Hesp) is developed. It is based on potentiometric monitoring of the concentration perturbations of the matrix reaction system which is in a stable non-equilibrium stationary state close to the bifurcation point. The Bray–Liebhafsky oscillatory reaction is used as the matrix system. The response of the matrix to perturbations by different concentrations of Hesp is followed by using a Pt electrode. A linear relationship between maximal potential shift and the logarithm of Hesp concentrations is obtained between 7.5 and 599.4 g mL^–1. The limit of detection is 0.65 g mL^–1. The described procedure has been successfully applied to the determination of Hesp from different sources (capsules, industrial and hand-squeezed orange juice, and white wine).     

Separation of carbohydrates by thin-layer chromatography

Summary The separation of 13 sugars by means of 8 solvents and one- and two-dimensional chromatography on cellulose and starch layers is described. Good results were obtained on cellulose layers.

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Zusammenfassung Die Trennung 13 verschiedener Zucker mit 8 Lösungsmitteln im Wege der ein- und zweidimensionalen Chromatographie auf Zelluloseund Stärkedünnschichten wurde beschrieben. Zelluloseschichten ergeben gute Resultate.

     

Application for optical thermometers calibration based on virtual instruments

In this paper we present a new developed application for calibration of optical thermometers which is implemented in the Serbian Metrology Institute. The method for calibration of optical thermometer–pyrometer is based on measuring blackbody temperature via thermocouple standards and measuring voltage on pyrometer in temperature range from 550 to 1650 °C. The objective is to precisely determinate calibration curve of pyrometer—transfer function. The metrology traceability was realized through thermocouples standard which has traceability to the international standard. A developed application has a role to control and supervise calibration process. Based on virtual instruments (VI), application offers monitoring measurement parameters in real time on three charts. The main advantage of the developed VI application is reduction of measurement uncertainty of type A by increased accuracy with multi—temperature measurement up to 3 thermocouples on temperature equilibrium in the measurement system and automatic data processing by converting voltage to temperature, calculating the mean value and standard deviation of the mean value. Advantage is also reflected in permanent data logging while application is running and low cost and user friendly interface One of the goals is to improve quality of metrological services through this application and support the establishment of a traceability chain to SI.     

Kinetic determination of morphine by means of Bray-Liebhafsky oscillatory reaction system using analyte pulse perturbation technique

A novel kinetic method for micro-quantitative determinations of morphine (MH) is proposed and validated. The method is based on the potentiometric monitoring of the concentration perturbations of the oscillatory reaction system being in a stable non-equilibrium stationary state close to the bifurcation point between stable and oscillatory state. The response of the Bray-Liebhafsky (BL) oscillatory reaction as a matrix system, to the perturbations by different concentrations of morphine, is followed by a Pt-electrode. The proposed method relies on the linear relationship between maximal potential shift, ΔE_m, and the logarithm of the added morphine amounts in the range of 0.004-0.18 μmol. Under optimum conditions, the sensitivity of the proposed method (as the limit of detection) is 0.001 μmol and the method is featured by good precision (R.S.D. = 1.6%) as well as the excellent sample throughput (45 samples h⁻¹). In addition to standard solution analysis, this approach was successfully applied for quantitative determination of morphine in a typical pharmaceutical dosage form. Some aspects of the possible mechanism of morphine action on the BL oscillating chemical system are discussed in detail.     

Stereochemical aspects of the controlled ring-opening polymerization of chiral cyclic esters

The stereochemical aspects of controlled polymerization of lactide and β-butyrolactone are discussed. The physicochemical and thermal properties of these polymers are shown to be depending on the stereochemical structure of the macromolecular chain. Different types of processes involving change of enantiomeric composition in the course of the polymerization reaction are examined in function of different initiators used. The formation of stereocomplexes from stereocopolymers of various enantiomeric compositions is reported.     

Dynamical time versus system time in quantum mechanics

Properties of an operator representing the dynamical time in the extended parameterization invariant formulation of quantum mechanics are studied. It is shown that this time operator is given by a positive operator measure analogously to the quantities that are known to represent various measurable time operators. The relation between the dynamical time of the extended formulation and the best known example of the system time operator, i.e., for the free one-dimensional particle, is obtained.