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Title: The contribution of electronically excited states to the radiation chemistry of organic systems

Technical Report ·
DOI:https://doi.org/10.2172/5119145· OSTI ID:5119145

The photocurrent from anthracene in 2,2,4-trimethylpentane, 2.2- dimethylbutane, cyclohexane, cyclopentane, and tetramethylsilane has been studied as a function of excitation energy from the ionization threshold to the onset of strong solvent absorption. The fluroescence from solutions of hexafluorobenzene in cyclopentane, 2,2,4-trimethylpentane, 2,2-dimethylbutane and tetramethylsilane irradiated with {beta}-particles has been studied as a function of the hexafluorobenzene concentration from c = 10{sup {minus}3}-10{sup {minus}1} M. The data are analyzed to permit extraction of the geminate ion-pair scavenging probability. The absorption of 160 nm light by cyclohexane in mixtures of cyclohexane, benzene and tetraphenylmethylenediamine results in an emission spectrum consisting of the simultaneous fluorescence from all three components. A mechanism for the development of this spectrum and its dependence on benzene concentration is constructed and shown to be quantitatively consistent with the results of independent measurements on the separate components. 55 refs.

Research Organization:
Minnesota Univ., Minneapolis, MN (United States). Dept. of Chemistry
Sponsoring Organization:
USDOE; USDOE, Washington, DC (United States)
DOE Contract Number:
FG02-85ER13404
OSTI ID:
5119145
Report Number(s):
DOE/ER/13404-6; ON: DE92001987
Country of Publication:
United States
Language:
English