Selective oxidation of CH4 and C2H6 over a mixed oxygen ion and electron conducting perovskite - A TAP and membrane reactors study

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autorschaft

  • Evgenii V. Kondratenko
  • Haihui Wang
  • Vita A. Kondratenko
  • Jürgen Caro

Externe Organisationen

  • Universität Rostock
  • South China University of Technology
Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Seiten (von - bis)142-149
Seitenumfang8
FachzeitschriftJournal of Molecular Catalysis A: Chemical
Jahrgang297
Ausgabenummer2
Frühes Online-Datum20 Sept. 2008
PublikationsstatusVeröffentlicht - 14 Jan. 2009

Abstract

In order to identify factors governing selectivity of an oxygen-conducting perovskite BaCoxFeyZrzO3-δ (BCFZ) membrane in the partial oxidation of methane and ethane, mechanistic aspects of product formation in these reactions were investigated with a millisecond time resolution using the temporal analysis of products (TAP) reactor. It was found that the selectivity depends on: (i) reduction degree of the perovskite surface; the higher the reduction degree, the higher the ethane and ethylene selectivity in methane and ethane oxidation, respectively, and (ii) contact time; short contact times favor partial selective oxidation. The influence of contact time on the ethylene selectivity in ethane oxidation at degrees of ethane conversion above 85% was experimentally proven in hollow fiber and disk membranes, which differ in the contact times. The low activity and selectivity in methane oxidation in the BCFZ perovskite membrane reactor were significantly increased, when the membrane on the hydrocarbon side was coated by a Ni-based steam reforming catalyst. This catalyst fulfils a double role: (i) it increases the oxygen transport through the perovskite membrane due to the high oxygen consumption, and (ii) it accelerates syngas production via deep methane oxidation followed by dry and steam reforming of methane. The syngas selectivity increases with an increase in the catalyst reduction degree, which is determined by the ratio of the rate of methane oxidation to the rate of oxygen permeation through the membrane.

ASJC Scopus Sachgebiete

Zitieren

Selective oxidation of CH4 and C2H6 over a mixed oxygen ion and electron conducting perovskite - A TAP and membrane reactors study. / Kondratenko, Evgenii V.; Wang, Haihui; Kondratenko, Vita A. et al.
in: Journal of Molecular Catalysis A: Chemical, Jahrgang 297, Nr. 2, 14.01.2009, S. 142-149.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Kondratenko EV, Wang H, Kondratenko VA, Caro J. Selective oxidation of CH4 and C2H6 over a mixed oxygen ion and electron conducting perovskite - A TAP and membrane reactors study. Journal of Molecular Catalysis A: Chemical. 2009 Jan 14;297(2):142-149. Epub 2008 Sep 20. doi: 10.1016/j.molcata.2008.09.015
Kondratenko, Evgenii V. ; Wang, Haihui ; Kondratenko, Vita A. et al. / Selective oxidation of CH4 and C2H6 over a mixed oxygen ion and electron conducting perovskite - A TAP and membrane reactors study. in: Journal of Molecular Catalysis A: Chemical. 2009 ; Jahrgang 297, Nr. 2. S. 142-149.
Download
@article{cbb6aa2813514ee7961f6375e6204457,
title = "Selective oxidation of CH4 and C2H6 over a mixed oxygen ion and electron conducting perovskite - A TAP and membrane reactors study",
abstract = "In order to identify factors governing selectivity of an oxygen-conducting perovskite BaCoxFeyZrzO3-δ (BCFZ) membrane in the partial oxidation of methane and ethane, mechanistic aspects of product formation in these reactions were investigated with a millisecond time resolution using the temporal analysis of products (TAP) reactor. It was found that the selectivity depends on: (i) reduction degree of the perovskite surface; the higher the reduction degree, the higher the ethane and ethylene selectivity in methane and ethane oxidation, respectively, and (ii) contact time; short contact times favor partial selective oxidation. The influence of contact time on the ethylene selectivity in ethane oxidation at degrees of ethane conversion above 85% was experimentally proven in hollow fiber and disk membranes, which differ in the contact times. The low activity and selectivity in methane oxidation in the BCFZ perovskite membrane reactor were significantly increased, when the membrane on the hydrocarbon side was coated by a Ni-based steam reforming catalyst. This catalyst fulfils a double role: (i) it increases the oxygen transport through the perovskite membrane due to the high oxygen consumption, and (ii) it accelerates syngas production via deep methane oxidation followed by dry and steam reforming of methane. The syngas selectivity increases with an increase in the catalyst reduction degree, which is determined by the ratio of the rate of methane oxidation to the rate of oxygen permeation through the membrane.",
keywords = "Membrane reactor, Mixed conductor, ODE, Perovskite, POM, Syngas, TAP",
author = "Kondratenko, {Evgenii V.} and Haihui Wang and Kondratenko, {Vita A.} and J{\"u}rgen Caro",
year = "2009",
month = jan,
day = "14",
doi = "10.1016/j.molcata.2008.09.015",
language = "English",
volume = "297",
pages = "142--149",
journal = "Journal of Molecular Catalysis A: Chemical",
issn = "1381-1169",
publisher = "Elsevier BV",
number = "2",

}

Download

TY - JOUR

T1 - Selective oxidation of CH4 and C2H6 over a mixed oxygen ion and electron conducting perovskite - A TAP and membrane reactors study

AU - Kondratenko, Evgenii V.

AU - Wang, Haihui

AU - Kondratenko, Vita A.

AU - Caro, Jürgen

PY - 2009/1/14

Y1 - 2009/1/14

N2 - In order to identify factors governing selectivity of an oxygen-conducting perovskite BaCoxFeyZrzO3-δ (BCFZ) membrane in the partial oxidation of methane and ethane, mechanistic aspects of product formation in these reactions were investigated with a millisecond time resolution using the temporal analysis of products (TAP) reactor. It was found that the selectivity depends on: (i) reduction degree of the perovskite surface; the higher the reduction degree, the higher the ethane and ethylene selectivity in methane and ethane oxidation, respectively, and (ii) contact time; short contact times favor partial selective oxidation. The influence of contact time on the ethylene selectivity in ethane oxidation at degrees of ethane conversion above 85% was experimentally proven in hollow fiber and disk membranes, which differ in the contact times. The low activity and selectivity in methane oxidation in the BCFZ perovskite membrane reactor were significantly increased, when the membrane on the hydrocarbon side was coated by a Ni-based steam reforming catalyst. This catalyst fulfils a double role: (i) it increases the oxygen transport through the perovskite membrane due to the high oxygen consumption, and (ii) it accelerates syngas production via deep methane oxidation followed by dry and steam reforming of methane. The syngas selectivity increases with an increase in the catalyst reduction degree, which is determined by the ratio of the rate of methane oxidation to the rate of oxygen permeation through the membrane.

AB - In order to identify factors governing selectivity of an oxygen-conducting perovskite BaCoxFeyZrzO3-δ (BCFZ) membrane in the partial oxidation of methane and ethane, mechanistic aspects of product formation in these reactions were investigated with a millisecond time resolution using the temporal analysis of products (TAP) reactor. It was found that the selectivity depends on: (i) reduction degree of the perovskite surface; the higher the reduction degree, the higher the ethane and ethylene selectivity in methane and ethane oxidation, respectively, and (ii) contact time; short contact times favor partial selective oxidation. The influence of contact time on the ethylene selectivity in ethane oxidation at degrees of ethane conversion above 85% was experimentally proven in hollow fiber and disk membranes, which differ in the contact times. The low activity and selectivity in methane oxidation in the BCFZ perovskite membrane reactor were significantly increased, when the membrane on the hydrocarbon side was coated by a Ni-based steam reforming catalyst. This catalyst fulfils a double role: (i) it increases the oxygen transport through the perovskite membrane due to the high oxygen consumption, and (ii) it accelerates syngas production via deep methane oxidation followed by dry and steam reforming of methane. The syngas selectivity increases with an increase in the catalyst reduction degree, which is determined by the ratio of the rate of methane oxidation to the rate of oxygen permeation through the membrane.

KW - Membrane reactor

KW - Mixed conductor

KW - ODE

KW - Perovskite

KW - POM

KW - Syngas

KW - TAP

UR - http://www.scopus.com/inward/record.url?scp=57749188958&partnerID=8YFLogxK

U2 - 10.1016/j.molcata.2008.09.015

DO - 10.1016/j.molcata.2008.09.015

M3 - Article

AN - SCOPUS:57749188958

VL - 297

SP - 142

EP - 149

JO - Journal of Molecular Catalysis A: Chemical

JF - Journal of Molecular Catalysis A: Chemical

SN - 1381-1169

IS - 2

ER -