Direct synthesis of oxygenates via partial oxidation of methane in the presence of O2 and H2 over a combination of Fe-ZSM-5 and Pd supported on an acid-functionalized porous polymer
[Display omitted] •Liquid-phase partial oxidation of methane with O2 was achieved in the presence of H2.•Pd supported on acid-functionalized porous polymer was used for in situ H2O2 generation.•Fe-ZSM-5 was stable and active for methane oxidation with in situ H2O2.•The combination of these two catal...
Gespeichert in:
Veröffentlicht in: | Applied catalysis. A, General General, 2020-07, Vol.602, p.117711, Article 117711 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | [Display omitted]
•Liquid-phase partial oxidation of methane with O2 was achieved in the presence of H2.•Pd supported on acid-functionalized porous polymer was used for in situ H2O2 generation.•Fe-ZSM-5 was stable and active for methane oxidation with in situ H2O2.•The combination of these two catalysts showed the TOF of 3.8 h−1 at 30 ℃.
Aqueous-phase partial oxidation of methane over a combination of heterogeneous Fe-ZSM-5 and Pd catalysts was demonstrated in the presence of O2 and H2. Fe-ZSM-5 catalyst active for partial oxidation of methane with H2O2 was prepared by an ion-exchange method. For comparison, homogeneous Fe species (FeSO4) were also used as a catalyst for partial oxidation of methane. Several supported Pd catalysts for the direct synthesis of hydrogen peroxide from H2 and O2 were prepared using activated carbon (AC), AC treated with sulfuric acid (s-AC), as-synthesized hyper-crosslinked porous polymer (HCPP), HCPP with carboxylic group (c−HCPP), and HCPP with carboxylic and sulfonic groups (c-s−HCPP). Among them, the Pd catalyst supported on c-s−HCPP was effective for generating H2O2in situ, which enabled methane oxidation over Fe-ZSM-5 without any leaching. |
---|---|
ISSN: | 0926-860X 1873-3875 |
DOI: | 10.1016/j.apcata.2020.117711 |