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Comparison of cracking and hydrocraking of n-heptane on H-ZSM-5 catalysts

โœ Scribed by Joachim Liers; Dr. rer. nat. Josefin Meusinger; Dr. rer. nat. habil. Wladimir Reschetilowski


Publisher
John Wiley and Sons
Year
1993
Tongue
English
Weight
651 KB
Volume
16
Category
Article
ISSN
0930-7516

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โœฆ Synopsis


Dedicated to Professor Emeritus Dr. Hanns Hofmann on the occasion of his 70th birthday

Acid catalyzed cracking and bifunctional cracking of n-heptane were investigated on H-ZSM-5 catalysts. At a reaction temperature of 543 K, the cracking on metal-free zeolite was found to be directly proportional to hydrogen partial pressure. Hydrogen influences the hydrogenation of product olefins and carbon deposits and therefore enhances the overall activity. Under the same conditions, in the presence of platinum, the hydrocracking rate reaches a maximum with increasing hydrogen partial pressure. The reaction can be formally described by a Langmuir Hinshelwood mechanism: hydrogen is adsorbed on Pt in competition with hydrocarbons. The maximum reaction rate depends on a favourable ratio of the two adsorbed reactants. The energy of activation of hydrocracking was over 100 kJ/mol higher than that of acid cracking.


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