A study is conducted to demonstrate catalytic dehydrogenation of light alkanes on metals and metal oxides. The study provides a complete overview of the materials used to catalyze this reaction, as dehydrogenation for the production of light olefins has become extremely relevant. Relevant factors, such as the specific nature of the active sites, as well as the effect of support, promoters, and reaction feed on catalyst performance and lifetime, are discussed for each catalytic Material. The study compares different catalysts in terms of the reaction mechanism and deactivation pathways and catalytic performance. The duration of the dehydrogenation step depends on the heat content of the catalyst bed, which decreases rapidly due to the endothermic nature of the reaction. Part of the heat required for the reaction is introduced to the reactors by preheating the reaction feed, additional heat being provided by adjacent reactors that are regenerating the coked catalysts.

Catalytic dehydrogenation of light alkanes on metals and metal oxides.

The dehydrogenation and aromatization of methane on modified ZSM-5 zeolite catalysts has been studied under non-oxidizing conditions with a fixed bed continuous-flow reactor and with a temperature programmed reactor. The results show that benzene is the only hydrocarbon product of the catalytic conversion of methane at high temperature (973 K). The catalytic activity of ZSM-5 is greatly improved by incorporating a metal cation (Mo or Zn). H2 and ethene have been directly detected in the products with a mass spectrometer during TPAR. A carbenium ion mechanism for the activation of methane is suggested.

Dehydrogenation and aromatization of methane under non-oxidizing conditions

Steam cracking of hydrocarbons has been the major source of light olefins for more than half a century. The recent studies have reported that ethylene and propylene can also be produced through the cracking of hydrocarbons over modified ZSM-5 zeolites in a considerable amount. This paper highlights the important current ideas about acid-catalyzed hydrocarbon cracking that has resulted in high yield of ethylene and propylene. Light olefin production via catalytic cracking of various industrial feedstocks, ranging from heavy hydrocarbons to ethane, over modified ZSM-5 zeolites, has been reviewed in the present paper. Furthermore, the influence of various employed promoters, i.e., alkali and alkaline earth, transition, rare earth elements, and phosphorus, on the chemical properties of the modified ZSM-5 and the performance of resulting catalyst in enhancing the selectivity to light olefins, have been addressed. Moreover, the influences of different factors, including the zeolite acidity, Si/Al ratio and the temperature, on the light olefin production and the reaction scheme have been specified. The role of incorporated element in the catalytic cracking mechanism is also summarized.

Catalytic cracking of hydrocarbons over modified ZSM-5 zeolites to produce light olefins: A review

Much attention has been paid to the transformation of lower alkanes such as propane and butanes into aromatic hydrocarbons from both industrial and academic points of view The aromatic hydrocarbons can be utilized as a booster for high octane number gasoline and are fundamental raw chemicals in petroleum chemistry The activation of lower alkanes is an intriguing subject In early work, Csicsery [1–5] described dehydrocyclodimerization of lower alkanes over bifunctional catalysts such as platinum on alumina and Cr2O3 on alumina

G. Creer

Papers

The reaction of propane over ZSM-5-H and ZSM-5-Zn zeolite catalysts