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P-modified deactivated TS-1: A benign catalyst for the MTP reaction.

Authors :
Lin, Yuxia
Xu, Deyi
Chen, Zhen
Yu, Yunkai
Li, Fang
Huang, Xin
Liu, Yueming
He, Mingyuan
Source :
Catalysis Today. Dec2022, Vol. 405, p258-266. 9p.
Publication Year :
2022

Abstract

Highly efficient catalyst is the core for the conversion of methanol to propylene (MTP). The deactivated TS-1 zeolite (De-TS-1) derived from the industrial ammoximation process has been successfully applied in the MTP reaction. After a series of systematic characterizations, the Si-OH groups adjacent to open Ti species (Si-OH(Ti) groups) were identified to be the active centers for the MTP reaction. Through further P modification on the acid-washed H-De-TS-1 zeolite, the obtained H-De-TS-1–0.4 P zeolite showed a better performance in the reaction. The total olefins selectivity and the single-run lifetime reached 87.9% and 91 h respectively and the hydrogen transfer index was as low as 0.11. This improvement could be attributed to the attenuated acid properties of H-De-TS-1–0.4 P zeolite, which suppressed the hydrogen transfer reactions, aromatization reactions and promoted the formation of olefins. During the process of P modification, phosphoric acid not only reacted with the Si-OH(Ti) groups to decrease the amount and strength of Brønsted acid sites, but also interacted with Ti-OH groups to transform the tetrahedral Ti species into octahedral ones and meanwhile decreased the amount and strength of Lewis acid sites. [Display omitted] • Si-(OH)Ti sites in the deactivated TS-1 were identified to be the active centers for the MTP reaction. • Phosphorus modification has been successfully applied on the deactivated TS-1. • Phosphoric acid reacted with not only the Si-OH(Ti), but also the Ti-OH. • The deactivated TS-1 as industrial discard solid waste was successfully recycled. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09205861
Volume :
405
Database :
Academic Search Index
Journal :
Catalysis Today
Publication Type :
Academic Journal
Accession number :
159857441
Full Text :
https://doi.org/10.1016/j.cattod.2022.04.034