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The coupling conversion of C6-C8 olefins and methanol over SAPO-34 is proposed for enhancing carbon resource utilization and light olefins production. With the aid of thermogravimetric analysis (TGA), dissolution-extraction experiment and molecular dynamics simulations, the relationship between reactive “coke” and reaction pathway of methanol-to-olefin (MTO) are studied. Owing to its remarkable product shape selectivity, octene is explored to be an effective coking source for promoting ethene production.
Evolution of confined species on pre-coked SAPO-34 illustrates the effect of polycyclic aromatics on product shape selectivity in MTO reaction. [Display omitted]
•Pre-coking strategies based on C6 – C8 olefins cracking are summarized.•The C2=/C3= ratio in production enhances by 40%.•Impact of HCP species on diffusional hindrances, product selectivity, etc. are elucidated.•The combined transition-state and product shape selectivity in MTO process is established.