Studies on the constituents of the green alga <Emphasis Type="Italic">Ulva lactuca</Emphasis>

Phytochemical investigations on a marine green alga Ulva lactuca led to the isolation of two new compounds (E)-6-heptacosen-5-one (1) and (E)-6-octadecen-5-ol (2), along with four known compounds, (Z)-10-hexacosene (3), docosanoic acid (4), palmitic acid (5), and isofucosterol (6). Compounds 3 and 4 were isolated for the first time from this species. The structures of the compounds were deduced with the help of modern spectroscopic techniques.     

An in situ STM/AFM and impedance spectroscopy study of the extremely pure 1-butyl-1-methylpyrrolidinium tris(pentafluoroethyl)trifluorophosphate/Au(111) interface: potential dependent solvation layers and the herringbone reconstruction

The structure and dynamics of the interfacial layers between the extremely pure air- and water-stable ionic liquid 1-butyl-1-methylpyrrolidinium tris(pentafluoroethyl)trifluorophosphate and Au(111) has been investigated using in situ scanning tunneling microscopy, cyclic voltammetry, electrochemical impedance spectroscopy, and atomic force microscopy measurements. The in situ scanning tunnelling microscopy measurements reveal that the Au(111) surface undergoes a reconstruction, and at -1.2 V versus Pt quasi-reference the famous (22 × √3) herringbone superstructure is probed. Atomic force microscopy measurements show that multiple ion pair layers are present at the ionic liquid/Au interface which are dependent on the electrode potential. Upon applying cathodic electrode potentials, stronger ionic liquid near surface structure is detected: both the number of near surface layers and the force required to rupture these layers increases. The electrochemical impedance spectroscopy results reveal that three distinct processes take place at the interface. The fastest process is capacitive in its low-frequency limit and is identified with electrochemical double layer formation. The differential electrochemical double layer capacitance exhibits a local maximum at -0.2 V versus Pt quasi-reference, which is most likely caused by changes in the orientation of cations in the innermost layer. In the potential range between -0.84 V and -1.04 V, a second capacitive process is observed which is slower than electrochemical double layer formation. This process seems to be related to the herringbone reconstruction. In the frequency range below 1 Hz, the onset of an ultraslow faradaic process is found. This process becomes faster when the electrode potential is shifted to more negative potentials.     

Polarization in the inelastic scattering of 185 MeV protons

The polarizations produced in the inelastic scattering of 185 MeV protons exciting the lowest octupole states in ¹²C and ²⁰⁸Pb are measured. The data together with earlier similar measurements for ⁴⁰Ca and ⁹⁰Zr are compared with existing theoretical models. The inclusion of a deformed spin-dependent interaction of the full Thomas form in the DWBA amplitude is found to considerably improve the theoretical fits to the data. For ¹²C, however, the DWBA fit is found to be inferior to that obtained using DWIA. The strong absorption model is found to give qualitatively good fits to the data for the heavier nuclei but again fails in the ¹²C case.     

Isothermal dimensional changes of some dental materials

The isothermal dimensional changes of four types of dental amalgams during the setting and for the next 24 hours after condensation have been studied by means of a Heraeus TA 500 thermal analysis system. The four types of dental amalgams were the lathe-cut conventional lowcopper amalgam (Amalcap), the spherical conventional low-copper amalgam (Spheralloy), the ternary unicomposition high-copper amalgam (Sybralloy) and the admixed high-copper (Dispersalloy) amalgam.The dimensional changes of the four types of amalgams are explained on the basis of their particle sizes and shapes and their constitutions.

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Zusammenfassung Mittels eines Heraeus TA 500 Thermoanalysensystemes wurden isotherme Größenveränderungen von Dentalamalgamen während des Setting und der 24 Stunden nach der Kondensation untersucht. Die Größenveränderungen der vier Amalgamgrundtypen (am Beispiel von Amalcap, Spheralloy, Sybralloy und Dispersalloy) wurden auf der Grundlage ihrer Teilchengröße und -form sowie auf der Grundlage ihrer Zusammensetzung erklärt.

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Determination of trace elements of Egyptian crops by neutron activation analysis

Multielemental neutron activation analysis was used for the determination of Al, As, Au, Br, Ca, Cd, Co, Cr, Cu, Fe, La, Mn, Mo, Sb, Se, W and Zn in African tea, and lady's fingers (Malvaceae Family), ginger (Zingiperaceae Family), canella bark (Laureceae Family), black pepper (Piperaceae Family), cucumber seeds and vegetable marrow seeds (Cucurbitaceae Family), tomatos seed (Solanaceae Family), safflower seeds (Compositae Family), jew's mallow seeds (Tiliaceae Family) and sesame (Pedaliaceae Family). Trace elements determination was made to the analysis of destructive (using super pure nitric acid and adsorbing the metal-APDC and metal-Dz complexes on activated charcoal) and nondestructive (dry seeds) samples. The method is simple, precise and sensitive for the determination of microamounts of the elements (ppm to ppb).     

Central collisions of24Mg nuclei with heavy emulsion group of nuclei (Br,Ag) at 4.5 AGeV/c momentum

Central collisions of²⁴Mg nuclei with the heavy (AgBr) group of emulsion nuclei are selected and analysed according to several selecting criteria. Theoretical calculations concerning cross sections for central events, average number of interacting protons from both projectile and target nuclei, multiplicity distributions of shower particles and dispersions, all based on the Glauber model, are performed to evaluate various criteria to select central events. The selection criterion based on the high multiplicity of total charged particles provides satisfactory agreement with the theoretical calculations.     

Relativistic DWBA calculations for polarization transfer in proton inelastic scattering

The matrix element for inelastic scattering of protons leading to the excitation of collective states in even-even nuclei is calculated in the framework of Dirac phenomenology using a DWBA approach. The deformed parts of the Lorentz scalar and four-vector optical potentials serve as the transition operators. The results are compared with the recently measured polarization transfer coefficients on ⁴⁰Ca and ²⁰⁸Pb at 500 MeV. The agreement with experiment is good.     

The transfer of momentum across surfaces drawn perpendicular to the direction of flow in gases under laminar conditions

Zusammenfassung Bei laminarer Strömung eines Gases ist die Übertragung der Bewegungsgrösse quer zu Flächen senkrecht zur Strömungsrichtung berechnet und gleich der transversalen Bewegungsgrösse quer zu Flächen, die parallel zur Strömungsrichtung laufen, gefunden worden. Daraus kann der Schluss gezogen werden, dass ein Flüssigkeitswürfel mit Seiten, die parallel zu den angegebenen Richtungen sind, statisch im Dreh-Gleichgewicht ist.