Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    ISSN: 1434-601X
    Keywords: 25.70.−z ; 25.70.Lm
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The competition between fusion-fission and deeply inelastic reactions in the Cl + Ni system has been studied by investigating the exit channelQ-value dependence of theZ-distributions of fission-like fragments. TheZ-, kinetic energy- and angular distributions of the fission-like fragments produced in the37Cl +64Ni system atE lab=170, 186 MeV and in the28Si +74Ge system atE lab=176 MeV have been measured by counter telescopes. TheZ-distribution of the37Cl +64Ni system was found to be essentially the same as that of the35Cl +62Ni system at the same bombarding energy. It is shown that this result can not be explained by the statistical fusion fission model but is consistent with a deeply inelastic model. A systematic study of the fission-like phenomenon in this mass region indicates that the maximum angular momenta for fusion reactions as well as the minimum angular momenta for DIC can be reproduced by the Bass model in the sliding limit (f=1.0) while the maximum angular momenta for fully energy-damped deeply inelastic reactions are governed by the strong interaction radius as predicted by the successive critical distance fusion model. The significance of these results are discussed.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 1434-601X
    Keywords: 25.70.Lm
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The energy damped reaction products from37Cl+12C,27Al,48Ti and16O+48Ti were measured over a wide range of angles (typically 18°〈θ lab〈70°), incident energies (160 〈E lab(37Cl)〈200 MeV,E lab(16O)=118 MeV) and charges Z, including two systems (37Cl+37Al and16O+48Ti) which lead to the same compound nucleus64Zn with the same excitation energy and comparable angular momenta. The angular dependences of total kinetic energy (TKE) and dσ/dθ were decomposed into two components (forward peaked and nearly constant at backward angles), and the elemental TKE and cross sections were derived. The backward components of37Cl+27Al and16O+48Ti exhibit very different Z-distributions, indicating that the fragments do not originate from compound nucleus decay. The results can be understood in terms of an energy damping process.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Reversed stationary phases ; Hydrophobic parameter ; Water/methanol eluent mixtures
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The hydrophobic retention characteristics of stationary ligands for reversed-phase high-performance liquid chromatography have been evaluated from the slope (r-value) of the plots relating the capacity factors (log k′) of selected aliphatic and aromatic compounds with the reciprocal of methanol concentration (log (1/[MeOH])) in aqueous mobile phase. Octadecylsilyl (ODS), trimethylsilyl (TMS) and phenyldimethylsilyl (phenyl) groups were selected as the stationary ligands bonded to silica support. On ODS or TMS silicas, unlike on phenyl silica, aliphatic compounds gave slightly larger r-values than aromatic compounds, indicating that the shape of the ligand recognizes the hydrophobic surfaces of aliphatic and aromatic solute molecules. On TMS and phenyl silicas, the degree of solute hydrophobicity contributing to its retention is about 90% and 85% of that on ODS silica, respectively. On the other hand, on TMS and phenyl silicas, the polar functional group on the solute molecule brought about a smaller decrease in retention than on ODS silica.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Hydrophobic parameter ; Capacity factor variation ; Organic modifier concentration ; Displacement model
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The dependence of the capacity factor (k′) on the concentration of the organic modifier (D) in the aqueous binary mobile phase in reversed-phase high-performance liquid chromatography has been investigated to evaluate the hydrophobicity of the solute molecule. The r-values, defined as the slope of log k′ vs. log(1/D) plots, were measured for various solutes and related to the non-polar surface area and the partition coefficients. The r-value was found to be a good indication of solute hydrophobicity. Detailed investigation of the results allowed to consider statistically the molecular posture of the solute adsorbed onto the stationary alkyl ligand.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...