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  • Canadian Science Publishing  (3)
  • Sagert, N. H.  (3)
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  • Canadian Science Publishing  (3)
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  • 1
    Online Resource
    Online Resource
    Canadian Science Publishing ; 1967
    In:  Canadian Journal of Chemistry Vol. 45, No. 12 ( 1967-06-15), p. 1351-1355
    In: Canadian Journal of Chemistry, Canadian Science Publishing, Vol. 45, No. 12 ( 1967-06-15), p. 1351-1355
    Abstract: Secondary reactions in the liquid phase radiolysis of cyclohexane in the presence of N 2 O and SF 6 have been examined by determining the yields of liquid products. When we added up to 0.3 M N 2 O, the hydrogen yield was reduced from its initial yield of 5.5 G units to 2.5 G units. The nitrogen yields were about twice the decrease in hydrogen yields. Bicyclohexyl and cyclohexene yields increased from their initial values to 2.2 7 and 3.5 0  G units respectively. When we added up to 0.12 M SF 6 , all the yields were decreased to about one half of their initial value.These results may be interpreted in terms of Dyne's general mechanism for the radiolysis of hydrocarbons if two cyclohexyl radicals are produced for every electron scavenged by N 2 O, but if none are produced for electrons scavenged by SF 6 . It is suggested that the total electron yield in pure cyclohexane is about 4.1 G units, of which only 3.0 G units produce hydrogen. The other 2.5 G units of hydrogen from the radiolysis of pure cyclohexane are presumed to arise from direct excitation.
    Type of Medium: Online Resource
    ISSN: 0008-4042 , 1480-3291
    RVK:
    Language: English
    Publisher: Canadian Science Publishing
    Publication Date: 1967
    detail.hit.zdb_id: 1482256-8
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  • 2
    Online Resource
    Online Resource
    Canadian Science Publishing ; 1968
    In:  Canadian Journal of Chemistry Vol. 46, No. 20 ( 1968-10-15), p. 3284-3287
    In: Canadian Journal of Chemistry, Canadian Science Publishing, Vol. 46, No. 20 ( 1968-10-15), p. 3284-3287
    Abstract: The radiolysis of cyclohexane in the vapor phase has been examined in the presence of up to 3 mole % perfluorocyclohexane. The results indicate that perfluorocyclohexyl radicals are produced with a yield of 2.0 G units at 3% perfluorocyclohexane. It is concluded that these radicals are formed when the perfluorocyclohexyl anions are neutralized. The relevance of this neutralization to the liquid phase radiolysis of cyclohexane is discussed.
    Type of Medium: Online Resource
    ISSN: 0008-4042 , 1480-3291
    RVK:
    Language: English
    Publisher: Canadian Science Publishing
    Publication Date: 1968
    detail.hit.zdb_id: 1482256-8
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  • 3
    Online Resource
    Online Resource
    Canadian Science Publishing ; 1968
    In:  Canadian Journal of Chemistry Vol. 46, No. 22 ( 1968-11-15), p. 3511-3516
    In: Canadian Journal of Chemistry, Canadian Science Publishing, Vol. 46, No. 22 ( 1968-11-15), p. 3511-3516
    Abstract: The γ-radiolysis of cyclohexane has been examined in the vapor phase using N 2 O and SF 6 as electron scavengers. Both N 2 O and SF 6 reduce the hydrogen yield from 4.6 to 3.0 G units, indicating that 3.0 G units of hydrogen have neutral species as precursors, while 1.6 G units have electrons as precursors.Radiolysis of cyclohexane vapor with more than 2% N 2 O produces 10.4 G units of cyclohexene and 11.5 of nitrogen. Carbon dioxide reduces both these yields; the extrapolated value of G(N 2 ) is equal to G(electrons) at infinite CO 2 concentration. Thus O − is likely a precursor of that part of the nitrogen yield in excess of G(electrons), and of the cyclohexene yield associated with this nitrogen yield.The first order molecular detachment of hydrogen is unaffected by electron scavengers, showing that most of this first order yield has neutral precursors. The implications for Dyne's general mechanism of hydrocarbon radiolysis are discussed.
    Type of Medium: Online Resource
    ISSN: 0008-4042 , 1480-3291
    RVK:
    Language: English
    Publisher: Canadian Science Publishing
    Publication Date: 1968
    detail.hit.zdb_id: 1482256-8
    Location Call Number Limitation Availability
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