Synthese und Geruch von (Z)-Dehydro-homo-β-santalol

Summary Guided by molecular modeling studies, the synthesis of the title compound is described. The organoleptic evaluation proved the predicted real sandal like odour of (Z)-dehydro-homo--santalol.

Aus den Diplomarbeiten von C.P. (1991), I.P. und B.Ö. (1992), Universität Wien     

Competitive adsorption and desorption of a bi-solute mixture: effect of activated carbon type

This study aims to clarify the effects of carbon activation type and physical form on the extent of adsorption capacity and desorption capacity of a bi-solute mixture of phenol and 2-chlorophenol (2-CP). For this purpose, two different PACs; thermally activated Norit SA4 and chemically activated Norit CA1, and their granular countertypes with similar physical characteristics, thermally activated Norit PKDA and chemically activated Norit CAgran, were used. The thermally activated carbons were better adsorbers for phenol and 2-CP compared with chemically activated carbons, but adsorption was more reversible in the latter case. 2-CP was adsorbed preferentially by each type of activated carbon, but adsorption of phenol was strongly suppressed in the presence of 2-CP. The simplified ideal adsorbed solution (SIAS) model underestimated the 2-CP loadings and overestimated the phenol loadings. However, the improved and modified forms of the SIAS model could better predict the competitive adsorption. The type of carbon activation was decisive in the application of these models. For each activated carbon type, phenol was desorbed more readily in the bi-solute case, but desorption of 2-CP was less compared with single-solute. This was attributed to higher energies of 2-CP adsorption.     

Radionuclides in a sediment trap and bottom sediment samples from the eastern Turkish coast of the Black Sea

Summary Radionuclide (¹³⁷Cs, ²³⁸U, ²³²Th and ⁴⁰K) concentrations were determined in a sediment trap and bottom sediment samples collected from a station at the eastern Turkish coast of the Black Sea. The specific activity of the ¹³⁷Cs radionuclide in the settling particles ranged from 0.04±0.01 to 0.10±0.02 Bq^. g^-1dry weight. The calculated flux rate of the ¹³⁷Cs was between 0.37 and 2.59 Bq^. m^-2. d^-1in the sampling periods of 2002 and 2003. The ¹³⁷Cs concentration in the bottom sediment profile were between 0.039±0.013-9.083±0.017 Bq^. g^-1dry weight in the same station. The vertical profile of the radionuclides suggests that they have little mobility during the 17 years after the Chernobyl accident.     

Determination of the stability constants of uranyl complex with 8-hydroxyquinolinium sulfate

8-Hydroxyquinoline (8-HOQ) is known as an important chelating agent for several metal ions. This compound is practically insoluble in water. For this reason, in this study its water soluble sulfate salt has been used for complexing uranyl ions and the stability constants of the complex have been determined. The Irving-Rosotti method computing the Calvin-Bjerrum pH-titration data, was applied. Finally, the stability constants of the complex formed between (8-HOQN-H)₂SO₄ and uranyl ions were found to be lgK₁=8.25 and lgK₂=4.15, the overall stability constant being {ie55-1}.     

99mTc-labelled human serum albumin: Chemical and electrochemical labelling methods

The labelling of human serum albumin /HSA/ with^99mTc has been investigated using a chemical method /stannous citrate/ and electrolytically generated tin/II/ ions. A comparative study of various chemical parameters and current intensities has been carried out in order to find the optimal conditions for labelling. The labelling yield was over 95%, for the chemical and electrolytical methods.     

Preparation of hollow beads of poly(styrene-co-divinyl benzene)

Two methods are described for the production of hollow beads by copolymerization of styrene and divinyl benzene. Characterization of the beads is described and growth mechanisms proposed.     

Elimination of bremsstrahlung in activation analysis by the deflection of β-particles in a magnetic field

The structureless background at X-ray and low energy -ray region, resulting from bremsstrahlung due to the stopping of -radiations, causes serious problems in nuclear spectroscopy. In this study, in order to reduce the background and therefore to increase the sensitivity of the nuclear analytical technique and the number of elements observable, a methodology is developed to deflect the -particles by a magnetic field. The experimental setup consists of a permanent magnet /1 kG/, Ge/Li/ solid-state detector, and multichannel analyzer.     

Determination of trace elements in Na-bentonitic clay by INAA in Turkey

Instrumental neutron activation analysis was applied to the determination of trace elements in a Na-bentonitic clay. The irradiation was done in the Triga Mark II type reactor of ITU Nuclear Energy Institute. The sample was irradiated in two steps for short- and long- lived isotopes. After irradiation, spectra were taken using a germanium detector, multichannel analyzer Canberra System 100 and a fitting program called Sampo 90. The spectra of short-lived isotopes were analyzed to determine Al, Mg, Na, K, Ca, Ti elements and Mn, V trace elements. The spectra of long-lived isotopes were analyzed to determine Sc, Br, Sb, Cs, La, Ce, Sm, Yb, Hf, Pa, Np trace elements.     

Leaching of uranium with the H2O2-Na2SO4-H2SO4 (HSS) system and the efficiency of Acigol Lake water

The applicability of a new leaching method, the HSS (H₂O₂-Na₂SO₄-H₂SO₄) system, in the extraction of uranium from Saricaolu-Bergama Region low grade ore, and the efficiency of Acigol Lake (Denizli)-Turkey water as a natural source of Na₂SO₄ has been investigated. The effect of H₂SO₄ concentration, temperature, leaching time, H₂O₂ and Na₂SO₄ concentrations and the amount of Acigol Lake water on the extraction of uranium was examined. HSS was found suitable for the extraction of uranium from Saricaolu-Bergama Region samples and it was observed that the acid consumption could be decreased by adding Na₂SO₄.     

NMR spectroscopy of organophosphorus compounds II: Stereochemistry of [1-(2H-azirin-2-yl)alkyl]phosphonates

Summary The conformation and relative configuration of [1-(2H-azirin-2-yl)alkyl]phosphonates (2) has been established by thorough investigation of some characteristic representatives of the series by¹H,¹³C,¹⁵N, and³¹P NMR spectroscopy. It is shown that the chemical shift of the proton located to the phosphonate group can be used as a criterion for the discrimination and stereochemical assignment of diastereoisomers. NMR spectroscopic features of the compounds are discussed in terms of structural relationships.Dedicated to Univ.-Prof. Dr.K. Schlögl with the best wishes to his 70^th birthday