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RADIATION CHEMISTRY OF ORGANIC COMPOUNDS. IV. CYCLOHEXANE

Journal Article · · Journal of Physical Chemistry (U.S.)
DOI:https://doi.org/10.1021/j150576a009· OSTI ID:4235633

The major products formed in the 800 kvp electron radiolysis of cyclohexane are hydrogen, cyclohexene, and dicyclohexyl. Minor amounts of products result from fragmentation and isomerization of the ring system. The initial yields are, G(C/sub 6/H/sub 10/) = 2.5 and G(dicpclohexyl) = 2.0 and were unchanged by irradiation either in 10 atmospheres of hydrogen or at liquid nitrogen temperature. In the presence of solutes, oxygen, iodine, and benzene, the cyclohenene yield decreased to a limiting value of G = O.T. The results are discussed in terms of a mechanism which involves the decomposition of excited cyclohexane molecules. The results show that of the excited molecules that decompose approximately 15% give products directly by an unspecified molecular process. (auth)

Research Organization:
General Electric Research Lab., Schenectady, N.Y.
Sponsoring Organization:
USDOE
NSA Number:
NSA-13-016044
OSTI ID:
4235633
Journal Information:
Journal of Physical Chemistry (U.S.), Journal Name: Journal of Physical Chemistry (U.S.) Vol. Vol: 63; ISSN JPCHA
Country of Publication:
Country unknown/Code not available
Language:
English

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