Reactions between alkenes and methanol or dimethyl ether (DME) on zeolite catalysts are involved in industrial processes that are highly relevant for the transition to renewable carbon sources, such as the Methanol-To-Hydrocarbons (MTH) process. In MTH chemistry, alkene methylation increases the length of product carbon chains, and its relative rate with respect to other reactions largely controls the overall selectivity. Experimental studies of alkene methylation present a considerable challenge because they are typically accompanied by cracking, hydrogen transfer, and aromatization reactions. Herein, the pulse-response Temporal Analysis of Products (TAP) methodology and complementary FTIR measurements were employed to isolate a well-defined population of surface species, consistent with Surface Methoxy Species (SMS) on Bronsted acid sites that are reactive in alkene methylation on a ZSM-22 (TON) zeolite. Their coverage was determined by TAP titration to be ca. 5% of the total amount of Brønsted acid sties, which was also indirectly suggested by FTIR data. C2-C4 alkenes were quantitatively reacted with SMS to precisely measure the intrinsic kinetic parameters of isolated alkene methylation steps. The rate constants increased and the activation energies decreased as functions of the carbon number (EC2H4 = 52 kJ/mol > EC3H6 = 32 kJ/mol > Ec-C4H8 = 16 kJ/mol). However, the rate constant for iso-butene was comparable to propene, despite its activation energy (Ei-C4H8 = 19 kJ/mol) being much lower than propene's. This effect is in agreement with the increased steric hindrance predicted by DFT for isobutene adsorption and methylation in TON zeolites. Our results considerably extend previously available TAP data on alkene methylation reactions and furthermore validate ab initio models of these crucial steps in the complex MTH chemistry on acidic zeolites.

A temporal analysis of products (TAP) study of C2-C4 alkene reactions with a well-defined pool of methylating species on ZSM-22 zeolite

Lazzarini A.;
2020

Abstract

Reactions between alkenes and methanol or dimethyl ether (DME) on zeolite catalysts are involved in industrial processes that are highly relevant for the transition to renewable carbon sources, such as the Methanol-To-Hydrocarbons (MTH) process. In MTH chemistry, alkene methylation increases the length of product carbon chains, and its relative rate with respect to other reactions largely controls the overall selectivity. Experimental studies of alkene methylation present a considerable challenge because they are typically accompanied by cracking, hydrogen transfer, and aromatization reactions. Herein, the pulse-response Temporal Analysis of Products (TAP) methodology and complementary FTIR measurements were employed to isolate a well-defined population of surface species, consistent with Surface Methoxy Species (SMS) on Bronsted acid sites that are reactive in alkene methylation on a ZSM-22 (TON) zeolite. Their coverage was determined by TAP titration to be ca. 5% of the total amount of Brønsted acid sties, which was also indirectly suggested by FTIR data. C2-C4 alkenes were quantitatively reacted with SMS to precisely measure the intrinsic kinetic parameters of isolated alkene methylation steps. The rate constants increased and the activation energies decreased as functions of the carbon number (EC2H4 = 52 kJ/mol > EC3H6 = 32 kJ/mol > Ec-C4H8 = 16 kJ/mol). However, the rate constant for iso-butene was comparable to propene, despite its activation energy (Ei-C4H8 = 19 kJ/mol) being much lower than propene's. This effect is in agreement with the increased steric hindrance predicted by DFT for isobutene adsorption and methylation in TON zeolites. Our results considerably extend previously available TAP data on alkene methylation reactions and furthermore validate ab initio models of these crucial steps in the complex MTH chemistry on acidic zeolites.
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11697/181773
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 10
  • ???jsp.display-item.citation.isi??? 8
social impact