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Mechanism of neopentane cracking over solid acids

Journal Article · · J. Catal.; (United States)

Neopentane was used as a probe to test whether catalyst protons can attack the C-C and/or the C-H sigma-bonds in the cracking of alkanes. Over a variety of solid acids approximately one CH/sub 4/ molecule was formed for every neopentane reacted. Moreover, in most cases nearly as much isobutene was formed. With H-Y zeolite (H-Y) and particularly with H-mordenite (H-M), however, hydride transfer leading to paraffin formation became important or dominant. Generally, the results conformed to (CH/sub 3/)/sub 3/C-H/sup +/-CH/sub 3/ ..-->.. CH/sub 4/ + (CH/sub 3/)/sub 3/C/sup +/ with the t-butyl ion either decomposing to isobutene or else undergoing secondary reactions. The latter tended to increase with the intensive factor of the acidity, i.e., with the strength of the acid-base interaction. The fraction of neopentane converted to CH/sub 4/, when plotted in the Arrhenius fashion against T/sup -1/, produced straight lines from which apparent activation energies could be calculated. Values obtained fell between 30 kcal/mol for silica-alumina and 14 kcal/mol for H-M (the most acidic and active catalyst investigated). Controversial views found in current literature are discussed in light of the present results.

Research Organization:
Univ. of Pittsburgh, PA (USA)
OSTI ID:
5259579
Journal Information:
J. Catal.; (United States), Journal Name: J. Catal.; (United States) Vol. 110:1; ISSN JCTLA
Country of Publication:
United States
Language:
English