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161.
162.
Ohne Zusammenfassung
Structural aspects for grain boundary segregation studies
  相似文献   
163.
Poly(γ-benzyl-L-glutamate) (PBLG), was utilized as a surface coating agent in order to obtain parallel molecular orientation in thin layers of PBLG liquid-crystalline solutions confined between coated surfaces. It was found that in a thickness range much larger than the cholesteric pitch value, the texture was predominantly planar cholesteric. At film thickness comparable or smaller than the pitch, isotropic spherulites developed from a homeotropic nematic phase. Because of the coupling between the solution concentration and nematic director, as well as large differences in the elastic moduli of PBLG liquid-crystalline solutions, the long-range intermolecular interaction was unfavorable. Competition between parallel orientation induced by the surface coating of PBLG and inherent perpendicular orientation induced by PBLG molecules in the bulk would favor a short-range helix-coil transition mechanism, which results into a reentrant isotropic phase.  相似文献   
164.
Ohne Zusammenfassung
Trace analysis of lead, cadmium and manganese in honey and sugar

Wir danken dem Fonds der Chemischen Industrie für finanzielle Unterstützung.  相似文献   
165.
166.
Catalytic activities of three transition metals, as iridium (III) chloride, rhodium (III) chloride and palladium (II) chloride, were compared in the oxidation of six aromatic aldehydes (benzaldehyde, p‐chloro benzaldehyde, p‐nitro benzaldehyde, m‐nitro benzaldehyde, p‐methoxy benzaldehyde and cinnamaldehyde), two hydrocarbons (viz. (anthracene and phenanthrene)) and one aromatic and one cyclic alcohol (cyclohexanol and benzyl alcohol) by 50% H2O2. The presence of traces (substrate: catalyst ratio equal to 1:62500 to 1:1961) of the chlorides of iridium(III), rhodium(III) and palladium(II) catalyze these oxidations, resulting in good to excellent yields. It was observed that in most of the cases palladium(II) chloride is the most efficient catalyst. Conditions for the highest and most economical yields were obtained. Deviation from the optimum conditions decreases the yields. Oxidation in aromatic aldehydes is selective at the aldehydeic group only and other groups remain unaffected. This new, simple and economical method, which is environmentally safe, also requires less time. Reactive species of catalysts, existing in the reaction mixture are also discussed. Copyright © 2007 John Wiley & Sons, Ltd.  相似文献   
167.
The effect of crack tip sharpness on crack propagation in vulcanized rubbers has been studied. For very sharp cracks, tearing is found to occur on a small scale at very low energies not far above the threshold required for the onset of mechanical crack growth. The “small-scale” tearing energies show relatively little variation for rubbers that differ widely in tear strength as normally measured. Thus the latter property appears to be strongly influenced by variations in the ability of rubbers to promote tip blunting. The small-scale tear behavior is of relevance to other fracture phenomena, including cutting by sharp objects and tensile failure. Natural variations in tip sharpness occur during cyclic or time-dependent mechanical crack growth and influence the form of the crack growth characteristics.  相似文献   
168.
The discharge behaviour of an atmospheric dielectric barrier parallel plate discharge, used for surface treatment, is studied. Since an uniform plasma is preferable for surface treatment, filaments must be avoided in the discharge. The occurrence of filaments can be detected by measuring the current flowing through the discharge. Current and voltage measurements give an indication of the power consumption by the plasma. The power consumption of the plasma as function of the applied frequency is examined. (© 2007 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   
169.
Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 55, No. 4, pp. 613–618, October, 1991.  相似文献   
170.
The QQ mass spectrometer is shown to be applicable to ion structure determination via collision-induced dissociations of mass-selected ions. The instrument can be scanned so as to record the products of dissociation as well as those of ion—molecule association reactions. The dissociations correspond to those observed at high kinetic energy in mass-analyzed ion kinetic energy spectrometers and the association reactions show parallels with reactions seen in ion cyclotron resonance spectroscopy and in high-pressure mass spectrometry  相似文献   
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