Ammonia pools effect in Cs modified X zeolites for side-chain alkylation of toluene with methanol
The strategy of in situ ammonia production from ammonia pools can modulate the Lewis acid-base pairs and distribution of alkali metal states in FAU zeolite, thereby constructing a superior catalyst for toluene side-chain alkylation. [Display omitted] •The ammonia pools effect (APE) modulates the Lew...
Gespeichert in:
Veröffentlicht in: | Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2023-10, Vol.474, p.145650, Article 145650 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | The strategy of in situ ammonia production from ammonia pools can modulate the Lewis acid-base pairs and distribution of alkali metal states in FAU zeolite, thereby constructing a superior catalyst for toluene side-chain alkylation.
[Display omitted]
•The ammonia pools effect (APE) modulates the Lewis acid-base pairs and Cs states in Cs-X zeolite.•The strategy of APE significantly promotes the performances for toluene side-chain alkylation.•the APE reduction contributes to the formation of the active intermediates of m-HCOO*.
Side-chain alkylation of toluene with methanol is a potential route for producing styrene. However, there are several challenges that prevent its industrialization, comprising the decomposition of methanol to CO and H2, and unavoidable by-products of ethylbenzene. Herein, we disclose that X zeolite after ion exchange of ammonium have an interesting and unexpected feature. It can modulate the Lewis acid-base pairs, via in situ ammonia production from ammonia pools, meanwhile, lead to more Cs+ species left in the zeolite, thereby constructing a superior catalyst for toluene side-chain alkylation. Especially for CsX-ex-AP catalyst, the ammonia pools effect (APE) in CsX-ex can achieve both higher toluene conversion and styrene selectivity. Furthermore, the methanol utilization efficiency increases significantly after APE reduction, indicating the selective catalysis for non-oxidative methanol dehydrogenation by in situ NH3 production from ammonia pools. In addition, the APE reduction contributes to the formation of the active intermediates of m-HCOO* species, which is another reason responsible for the superior performance. |
---|---|
ISSN: | 1385-8947 1873-3212 |
DOI: | 10.1016/j.cej.2023.145650 |