Scalar gluonium candidates and the radiativeJ/ψ decays

We discuss productions of scalar gluonium candidates in the radiativeJ/ decays. The branching ratios of such productions are estimated on the basis of the Euler-Heisenberg effective Lagrangian for gluon-photon couplings. We mention that these estimates cannot be expected to be accurate to better than within a factor 2. We show that the radiativeJ/ decays probably invalidate gluoniumgg interpretation of the GAMS meson F₀(1590) and a narrow 0⁺⁺ stateS lying below 1 GeV. However, a possible wide scalar effective gluonium candidate(920) is shown not to be excluded by the data on the decayJ/. We also find that the experimental data about radiativeJ/ decays presumably agree with a recently suggested interpretation of F₀(1590) as being approximately a half-and-half mixture of pure 0⁺⁺ gluoniumgg andSU(3)_f singlet quarkoniumq¯q states.     

Investigation of 2-[(<Emphasis Type="Italic">E</Emphasis>)-2-(4-diethylaminophenyl)-1-ethenyl]-1,3,3-trimethyl-3H-indolium as a new highly sensitive reagent for the spectrophotometric determination of nitrophenols

A new, simple, rapid, and sensitive spectrophotometric method has been developed for the determination of nitrophenols [picric acid (PA); dinitrophenols (DNP)] in wastewater samples. The method is based on the reaction of nitrophenols with 2-[(E)-2-(4-diethylaminophenyl)-1-ethenyl]-1,3,3-trimethyl-3 H-indolium chloride reagent to form the colored ion associates, which are extracted by organic solvents. The molar absorptivity of the ion associates of PA with the investigated reagent ranges from 8.3×10⁴ to 11.3×10⁴ L mol^–1 cm^–1, depending on the extractant. Because only PA is extracted in an acidic medium with the investigated reagent, but both PA and DNP are extracted in an alkaline medium, it is possible to determine both substances in a mixture. Appropriate reaction conditions have been established. The absorbance of the colored extracts obeys Beers law in the range of 0.04–4.58 mg L^–1 PA, 1.0–18.4 mg L^–1 2,4-DNP and 1.2–14.7 mg L^–1 2,6-DNP, respectively. The limit of detections, calculated from a blank test (n=10; P=0.95), are 0.05 mg L^–1 PA, 0.9 mg L^–1 (2,4-DNP), and 1.1 mg L^–1 (2,6-DNP), respectively.     

Some problems concerning the use of automated radiochemical separation systems in destructive neutron activation analysis

The present state of a long term program is reviewed. It was started to elaborate a remote controlled automated radiochemical processing system for the neutron activation analysis of biological materials. The system is based on wet ashing of the sample, followed by reactive desorption of some volatile components. The distillation residue is passed through a series of columns filled with selective ion screening materials to remove the matrix activity. The solution is thus “stripped” from the interfering radioions, and it is processed to single-elements through group separations using ion-exchange chromatographic techniques. Some special problems concerning this system are treated. (a) General aspects of the construction of a (semi)automated radiochemical processing system are discussed; (b) Comparison is made between various technical realizations of the same basic concept; (c) Some problems concerning the “reconstruction” of an already published processing system are outlined.     

Temperature Development of Homo- and Hetero-Clustering in Saturated Vapors

Computational findings of temperature increase of clustering degree in saturated vapors are analyzed. A thermodynamic proof is presented and a simple criterion derived. Illustrations are based on saturated steam, magnesium and carbon vapor. The results are applicable to synthesis of fullerenes, metallofullerenes, and heterofullerenes, chemical vapor deposition technique, or atmospheric chemistry.     

Emanation Thermal Analysis of SiC Based Materials

Results of emanation thermal analysis (ETA) characterizing microstructure changes of SiC based materials during heat treatment in argon are demonstrated. This method made it possible to reveal fine changes of the texture of SiC nano-sized powders, SiC micro-sized powders and SiC whiskers under in situconditions of the heating. ETA curves can serve as fingerprints of the respective samples.This revised version was published online in November 2005 with corrections to the Cover Date.     

Filiation structurale des phases de´rive´es de BaFeF5

Au sein d'un re´seau de type BaFeF₅ des chai?nes d'octae`dres fluore´sa`sommets communs peuvent disparai?tre en donnant naissance a des canaux dont l'occupation partielle ou totale par des files de cations Sr²⁺ et de couples d'anions F^?, conduit respectivement aux phases Sr₃(FeF₆)₂ ou Sr₅T₃F₁₉ (T = Cr, Co, Ga). Une discussion cristallochimique permet d'expliquer l'existence d'un domaine de solutions solides au sein du diagramme ternaire SrF₂BaF₂FeF₃.     

X-ray investigation of the role of the mixed emulsifier in the structure formation in o/w creams

The aim of this research work was to clarify the role of the mixed emulsifier in the structure formation and water binding mode in the case of o/w creams prepared with different surfactants. The swelling behavior of mixed emulsifiers was examined by means of direct investigation methods such as transmission electron microscopy (TEM) and X-ray diffraction. The detailed structure image of the creams was created with the help of the latter. The influence of the structure of the hydrophilic gel phase, and the structural changes during storage were studied with rheological methods. On the basis of the results, it can be stated that the investigated creams had different structures from those mentioned in the literature: surfactant did not create a mixed bilayer with the structure to furnish fatty amphiphile; instead, micelles were formed. These results correlated well with the results of the rheological tests.     

PPP-Berechnungen und Vergleich der Elektronenspektren von iso-π-elektronischen Sauerstoff-, Stickstoff-, Schwefel- und Selenheterocyclen

Zusammenfassung 42 Heterocyclen, die sich formal von alternierenden und nichtalternierenden Kohlenwasserstoffen durch Ersatz einer Doppelbindung durch die Heteroatome Sauerstoff, Stickstoff, Schwefel und Selen ableiten, werden nach dem Pariser-Parr-Pople-Verfahren berechnet und ihre Spektren im nahen Ultraviolett und Sichtbaren beschrieben. Schwefel und Selen werden dabei im LCAO-MO-Verfahren nach dem p-Modell behandelt. In den meisten Fällen können die Berechnungen nicht nur die spektralen Charakteristika gut wiedergeben, sondern auch Beziehungen in den Spektren iso--elektronischer Verbindungen gleicher Struktur verständlich machen. Berechnungen an kationischen Stickstoffheterocyclen führten dann zu falschen Ergebnissen, wenn die Stickstoffparameter vom Pyrroltyp übernommen werden.

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PPP-calculations and comparison of electronic spectra of iso--electronic oxygen, nitrogen, sulfur, and selenium heterocycles

42 heterocyclic compounds, formally derived from alternant or nonalternant hydrocarbons by replacing a C=C group by an oxygen, nitrogen, sulfur or selenium atom, are studied by the Pariser-Parr-Pople-type of calculation. By means of these results the near ultraviolet and visible spectra are described. The sulfur and the selenium atoms are treated in the LCAO-MO-method using the p-model. In most cases spectral features are not only well reproduced, but interrelations of the spectra of iso--electronic compounds, possessing analogous structures are interpreted, too. On calculating cationic nitrogen heterocycles using parameters of pyrrol type nitrogen results are unsatisfactory.

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Résumé 42 composés hétérocycliques, formellement dérivés d'hydrocarbures alternants ou non alternants par remplacement d'un groupement C=C par un atome d'oxygène, d'azote, de soufre ou de sélénium, sont étudiés par la méthode de Pariser-Parr-Pople. Les résultats obtenus permettent de décrire le spectre U.V. proche et visible. Soufre et sélénium sont traités en utilisant le modèle p. Dans la plupart des cas les caractères spectraux sont non seulement correctement reproduits, mais les relations entre les spectres des composés iso--électroniques à structures analogues peuvent être interprétées. Les calculs concernant les heterocycles à azote cationique sont insatisfaisants lorsqu'ils sont effectués avec des paramètres de l'azote du type pyrrole.

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Anmerkung: Die Arbeit wurde in dem von Prof. Dr. R. Mayer geleiteten Schwefelarbeitskreis der TU Dresden durchgeführt.