THE MECHANISM OF HYDROGEN FORMATION IN THE RADIOLYSIS OF CYCLOHEXANE AND OTHER HYDROCARBONS
The gamma radiolyses of liquid alkanes with and without added iodine and methyl iodide or olefins were investigated. The systems and yields were: G(H/ sub 2/), G(CH/sub 4/), and G(HI) in cyclopertane, n-hexane, 3-methylpentane, and Z,4-dimethylpontane, each containing 2 x 10/sup -2/ M iodine and up to 0.8M methyl iodide; G(c-C/sub 5/H/sub 8/) and G(c-C/sub 5/H/sub 9/I) in cyclopentane methyl iodine; G(c-C/sub 6/H/sub 10/), G(c-C/sub 6/H/sub 11/I), and G(C/sub 12/H / sub 22/) in cyclohexane - methyl iodide - iodine; G (H/sub 2/), G(HD), and G(D/ sub 2/) for 1% cyclohexene-d/sub 10/ in cyclohexane and 1.5% cycyclohexene-d/sub 10/ in cyclopertane. Ultraviolet absorption of products was measured in vacuo for cyclohexane, cyclopertane, n-hexane, 0.05M cyclohexene in cyclohexane, and 0.05M cyclopentene in n-hexane at 20 deg C, and for 0.1M cyclohexene and 0.1M cyclopentene in 3-methylpentane glass at --196 deg C. The results are interpreted in terms of electron attachment and charge transfer as well as freeradical reactions. A yield of 0.5 molecule/100 ev or greater was found in cyclohexane for an organic product not previously reported. (auth)
- Research Organization:
- Univ. of Notre Dame, Ind.
- Sponsoring Organization:
- USDOE
- NSA Number:
- NSA-18-020057
- OSTI ID:
- 4030617
- Journal Information:
- Journal of the American Chemical Society (U.S.), Journal Name: Journal of the American Chemical Society (U.S.) Vol. Vol: 86; ISSN JACSA
- Country of Publication:
- Country unknown/Code not available
- Language:
- English
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Related Subjects
BINDING ENERGY
CHEMISTRY
CYCLOALKANES
CYCLOALKENES
DECOMPOSITION
DEUTERIUM
DEUTERIUM COMPOUNDS
FREE RADICALS
G-VALUE
HEXANE
HYDROGEN
HYDROIODIC ACID
IODIDES
IODINE
MEASURED VALUES
METHANE
METHYL RADICALS
ORGANIC IODINE COMPOUNDS
PENTANE
RADIATION CHEMISTRY
RADIOLYSIS
REACTION KINETICS
ULTRAVIOLET RADIATION
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